Paint, Construction, Plastics, Rubber Chemicals

ORP 7680 SL
ORP 7680 SL: Redispersible Powder for Self Leveling Dry-Mix Mortars. ORP 7680 SL is a redispersible powder polymer produced by drying an emulsion of Vinyl Acetate / Acrylic copolymer with PVOH as protective colloid. The specific chemical composition of the polymer ORP 7680 SL allows coalescence of the redispersed polymer at low temperatures and provides good adhesion to cementitious substrates. ORP 7680 SL is used to modify mixtures containing hydraulic binders. Due to its particular chemical and physical composition, ORP 7680 SL improves adhesion, flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially in self levelling mortar formulations ORP 7680 SL provides excellent abrasion resistance, flexural & compressive stength and good leveling. ORP 7680 SL IS A REDISPERSIBLE POWDER POLYMER FOR SELF LEVELLING DRY-MIX MORTARS TYPICAL PROPERTIES Appearance: White powder Chemical composition: VA / Acrylic Copolymer Stabilizing System: PVOH Residual Humidity (%): Max. 2.0 Bulk Density (g/l): 400 - 600 Ash Content (%): 12 ± 2 Alkali Resistance: High After 1:1 Dispersion with Water MFFT (°C):5 ± 1 APPLICATION AREAS ORP 7680 SL can be used between 1.5 – 4.0 % in self leveling mortar formulations. This amount of usage provides high abrasion resistance, water resistance, flexural & compressive strength. Also decreases segmentation and efflorescence. PRODUCT HANDLING – STORAGE – SHELF LIFE Packaging: Pallet with 18 paper bags, each 25 kg, also 500 or 1000 kg of big bags. Packages must be stored in a dry and cool warehouse. Pallets must not be stacked on top of each other to avoid caking due to the thermoplasticity of the polymer. Packing must be closed well after usage for protection against humidity and caking. ORP 7680 SL has to be used within 6 months after the date of delivery. Construction Solutions In the ever changing and demanding construction market, innovative solutions, product quality and fast delivery to the market have been integral to respond to the market needs. Ataman Kimya, supplying polymer emulsions to various markets since 1980 s, established a dedicated “Construction Solutions” business unit to better answer the needs of this industry. With its dedicated Research & Development, Sales, Marketing and Technical Solutions Teams, Ataman Kimya’s Construction Solutions Business Unit understands and delivers customer expectations. The dedicated Research & Development and Commercial Teams have also been crowned with the inauguration of redispersible powder polymer plant. Today, ATAMAN CHEMICALS supplies the market with polymer emulsions, redispersible powder polymers and specialty additives. Polymer Emulsions Offering a wide array of styrene, vinyl acetate and acrylic chemical compositions, ATAMAN CHEMICALS offers innovative solutions with various polymerization technologies for the cementitious and dispersion based construction chemicals markets. Redispersible Powder Polymers ATAMAN CHEMICALS provides solutions in carbon rich monomer combinations of vinyl versatate and acrylics that highlight properties such as water resistance, saponification resistance and flexibility. Specialty Additives Acrylic associative and non-associative rheology modifiers specifically are designed for fullfilling different application rheology requirements of different markets. Dispersion agents, both ammonia or sodium based salts, are able to work with different dispersing systems and chemistries. Rheology modifiers and dispersion agents are used in both dispersion based and liquid components of 2K Cementitious Systems. Technical Solution Partnership Approach of ATAMAN has dedicated synthesis and application laboratories within Research & Development Center With state of the art equipment, ATAMAN is able to perform all application and analysis tests in accordance with the regional and international standards Customer intimacy and solving customer needs is of utmost importance to ATAMAN; therefore, joint projects and testing for customers at the laboratories are executed with much diligence
ORP HYDROFLEX 64
ORP Hydroflex 64 is Hydrophobically Modified Redispersible Powder for Dry-Mix Mortars. ORP Hydroflex 64 is a redispersible powder produced by drying an emulsion of Vinyl Acetate / Vinyl Versatate / Acrylic terpolymer with PVOH as protective colloid. The specific chemical composition of the polymer allows coalescence of the redispersed polymer at low temperatures and provides good adhesion on mineral substrates. ORP Hydroflex 64 is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP Hydroflex 64 improves adhesion, flexibility, hydrophobicity and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially because of the flexible nature, ORP Hydroflex 64 performs very well in transverse deformation conditions. TYPICAL PROPERTIES Appearance: White powder Chemical composition: VA / VV / Acrylic Terpolymer Stabilizing System: PVOH Residual Humidity (%): Max. 2.0 Bulk Density (g/l):350 - 550 Ash Content (%):12 ± 2 Alkali Resistance: High After 1:1 Dispersion with Water MFFT (°C): 0 ±1 APPLICATION AREAS ORP Hydroflex 64 can be used in mortar formulations where highly flexbily/elastic, hydrophobic and water resistant behavior is required at the same time. In high performance of ceramic tile grouts formulations (CG2) ORP Hydroflex 64 can be used with the ratio of 2.0 – 4.0 % in weight and without requiring an additional hydrophobic agent. Moreover ORP Hydroflex 64 is a very suitable redispersible powder polymer for cementitious water proofing mortars. It can be used with the ratio of 7.0 – 12.0 % in weight in 1K cementitious water proofing mortar formulations. Because of its molecular structure it provides high crack bridging ability. Also ORP Hydroflex 64 performs very well in cementitious exterior plasters and topcoats with the amunt of 2.0 – 4.0 %. PRODUCT HANDLING – STORAGE – SHELFLIFE Packaging: Pallet with 18 paper bags, each 25 kg, also 500 or 1000 kg of big bags. Packages must be stored in a dry and cool warehouse. Pallets must not be stacked on top of each other to avoid caking due to the thermoplasticity of the polymer. Packing must be closed well after usage for protection against humidity and caking. It has to be used within 6 months after the date of delivery. Today, ATAMAN CHEMICALS supplies the market with polymer emulsions, redispersible powder polymers and specialty additives. Polymer Emulsions Offering a wide array of styrene, vinyl acetate and acrylic chemical compositions, ATAMAN CHEMICALS offers innovative solutions with various polymerization technologies for the cementitious and dispersion based construction chemicals markets. Redispersible Powder Polymers ATAMAN CHEMICALS provides solutions in carbon rich monomer combinations of vinyl versatate and acrylics that highlight properties such as water resistance, saponification resistance and flexibility. Specialty Additives Acrylic associative and non-associative rheology modifiers specifically are designed for fullfilling different application rheology requirements of different markets. Dispersion agents, both ammonia or sodium based salts, are able to work with different dispersing systems and chemistries. Rheology modifiers and dispersion agents are used in both dispersion based and liquid components of 2K Cementitious Systems. Technical Solution Partnership Approach of ATAMAN has dedicated synthesis and application laboratories within Research & Development Center With state of the art equipment, ATAMAN is able to perform all application and analysis tests in accordance with the regional and international standards Customer intimacy and solving customer needs is of utmost importance to ATAMAN; therefore, joint projects and testing for customers at the laboratories are executed with much diligence
ORP HYDROFLEX 64
ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) ORP Hydroflex 64 is a redispersible powder produced by drying an emulsion of Vinyl Acetate / Vinyl Versatate / Acrylic terpolymer with PVOH as protective colloid. The specific chemical composition of the polymer allows coalescence of the redispersed polymer at low temperatures and provides good adhesion on mineral substrates. ORP Hydroflex 64 is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP Hydroflex 64 improves adhesion, flexibility, hydrophobicity and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially because of the flexible nature, ORP Hydroflex 64 performs very well in transverse deformation conditions. TYPICAL PROPERTIES of ORP Hydroflex 64 Appearance Chemical composition Stabilizing System Residual Humidity (%) Bulk Density (g/l) Ash Content (%) Alkali Resistance After 1:1 Dispersion with Water MFFT (°C) White powder VA / VV / Acrylic Terpolymer PVOH Max. 2.0 350 - 550 12 ± 2 High 0 ±1 APPLICATION AREAS of ORP Hydroflex 64 ORP Hydroflex 64 can be used in mortar formulations where highly flexbily/elastic, hydrophobic and water resistant behavior is required at the same time. In high performance of ceramic tile grouts formulations (CG2) ORP Hydroflex 64 can be used with the ratio of 2.0 - 4.0 % in weight and without requiring an additional hydrophobic agent. Moreover ORP Hydroflex 64 is a very suitable redispersible powder polymer for cementitious water proofing mortars.It can be used with the ratio of 7.0 - 12.0 % in weight in 1K cementitious water proofing mortar formulations. Because of its molecular structure it provides high crack bridging ability. Also ORP Hydroflex 64 performs very well in cementitious exterior plasters and topcoats with the amunt of 2.0 - 4.0 %. PRODUCT HANDLING - STORAGE - SHELFLIFE of ORP Hydroflex 64 Packaging: Pallet with 18 paper bags, each 25 kg, also 500 or 1000 kg of big bags. Packages must be stored in a dry and cool warehouse. Pallets must not be stacked on top of each other to avoid caking due to the thermoplasticity of the polymer. Packing must be closed well after usage for protection against humidity and caking. It has to be used within 6 months after the date of delivery. 1.1. Product identifier Product name ORP HYDROFLEX 64 Chemical name and synonym Vinyl Acetate l VeoVa l Acrylic terpolymer 1.2. Relevant identified uses of the substance or mixture and uses advised against Intended use Redispersible Powder for Dry-Mix Mortars . Mixtures The product does not contain substances classified as being hazardous to human health or the environment pursuant to the provisions Regulation (EU) 1272/2008 (CLP) (and subsequent amendments and supplements) in such quantities as to require the statement. . Information on basic physical and chemical properties Appearance powder Colour white Odour characteristic Odour threshold Not available pH 5,0-8,0 (1:1 aqueous soln.) ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is an organic compound with the formula CH3CO2CH=CH2. This colorless liquid is the precursor to polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM), an important industrial polymer.[3] Contents 1 Production of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) 2 Preparation of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) 2.1 Mechanism of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) 2.2 Alternative routes 3 Polymerization of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) 4 Other reactions of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) 5 Toxicity evaluation of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) 6 See also 7 References 8 External links Production of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) The worldwide production capacity of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) was estimated at 6,969,000 tonnes/year in 2007, with most capacity concentrated in the United States (1,585,000 all in Texas), China (1,261,000), Japan (725,000) and Taiwan (650,000).[4] The average list price for 2008 was $1600/tonne. Celanese is the largest producer (ca 25% of the worldwide capacity), while other significant producers include China Petrochemical Corporation (7%), Chang Chun Group (6%), and LyondellBasell (5%).[4] It is a key ingredient in furniture glue.[5] Preparation ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is the acetate ester of vinyl alcohol. Since vinyl alcohol is highly unstable (with respect to acetaldehyde), the preparation of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is more complex than the synthesis of other acetate esters. The major industrial route involves the reaction of ethylene and acetic acid with oxygen in the presence of a palladium catalyst.[6] {\displaystyle {\ce {2 C2H4 + 2 CH3CO2H + O2 -> 2 CH3CO2CHCH2 + 2 H2O}}}{\displaystyle {\ce {2 C2H4 + 2 CH3CO2H + O2 -> 2 CH3CO2CHCH2 + 2 H2O}}} The main side reaction is the combustion of organic precursors. Mechanism Isotope labeling and kinetics experiments suggest that the mechanism involves PdCH2CH2OAc-containing intermediates. Beta-hydride elimination would generate ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) and a palladium hydride, which would be oxidized to give hydroxide.[7] Alternative routes ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) was once prepared by hydroesterification. This method involves the gas-phase addition of acetic acid to acetylene in the presence of metal catalysts. By this route, using mercury(II) catalysts, ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) was first prepared by Fritz Klatte in 1912.[3] Another route to ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) involves thermal decomposition of ethylidene diacetate: {\displaystyle {\ce {(CH3CO2)2CHCH3 -> CH3CO2CHCH2 + CH3CO2H}}}{\displaystyle {\ce {(CH3CO2)2CHCH3 -> CH3CO2CHCH2 + CH3CO2H}}} Polymerization It can be polymerized to give polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) (PVA). With other monomers it can be used to prepare various copolymers such as ethylene-ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) (EVA), ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM)-acrylic acid (VA/AA), polyvinyl chloride acetate (PVCA), and polyvinylpyrrolidone (Vp/Va Copolymer, used in hair gels).[8] Due to the instability of the radical, attempts to control the polymerization via most 'living/controlled' radical processes have proved problematic. However, RAFT (or more specifically MADIX) polymerization offers a convenient method of controlling the synthesis of PVA by the addition of a xanthate or a dithiocarbamate chain transfer agent. Other reactions ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) undergoes many of the reactions anticipated for an alkene and an ester. Bromine adds to give the dibromide. Hydrogen halides add to give 1-haloethyl acetates, which cannot be generated by other methods because of the non-availability of the corresponding halo-alcohols. Acetic acid adds in the presence of palladium catalysts to give ethylidene diacetate, CH3CH(OAc)2. It undergoes transesterification with a variety of carboxylic acids.[9] The alkene also undergoes Diels-Alder and 2+2 cycloadditions. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) undergoes transesterification, giving access to vinyl ethers:[10][11] ROH + CH2=CHOAc → ROCH=CH2 + HOAc Toxicity evaluation Tests suggest that ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is of low toxicity. For rats (oral) LD50 is 2920 mg/kg.[3] On January 31, 2009, the Government of Canada's final assessment concluded that exposure to ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is not harmful to human health.[12] This decision under the Canadian Environmental Protection Act (CEPA) was based on new information received during the public comment period, as well as more recent information from the risk assessment conducted by the European Union. It is classified as an extremely hazardous substance in the United States as defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. 11002), and is subject to strict reporting requirements by facilities which produce, store, or use it in significant quantities. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) appears as a clear colorless liquid. Flash point 18°F. Density 7.8 lb / gal. Slightly soluble in water. Vapors are heavier than air. Vapors irritate the eyes and respiratory system. May polymerize if heated or contaminated. If polymerization occurs inside a container, the container may violently rupture. Used to make adhesives, paints, and plastics. At 20 °C, a saturated solution of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) in water contains 2.0-2.4 wt % ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM), whereas a saturated solution of water in ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) contains 0.9-1.0 wt % water; at 50 °C, the solubility of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) in water is 0.1 wt % more than at 20 °C, but the solubility of water in ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) doubles to about 2 wt % The/ fate of inhaled ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) in rabbits /was studied/. ... ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) tended to remain in the body after it was inhaled; 70% of the ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) administered was retained, and an equilibrium was established in the first few min after exposure began. ... No ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) /was found/ in the blood, either during or after its inhalation, which suggested ... that ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is rapidly metabolized when it enters the body through the lungs. Two male Wistar Rats exposed to ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) (stabilized with 0.01% hydroquinone) concentrations varying between 200 and 2000 ppm in closed chambers with an exposure time of 1.4 hr or less demonstrated dose dependent elimination kinetics. The authors concluded that the metabolic pathways became saturated when ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) exposure levels exceeded 650 ppm (2320 mg/cu m). ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) deposition was measured in the isolated upper respiratory tract (URT) of anaesthetized adult male CrlCD:BR rats at exposure concentrations ranging from 73 to 2190 ppm during 1 hr inhalation under unidirectional flow conditions (flow rate 100 mL/min) ... Preliminary experiments showed that approximately 8 min of exposure was required for ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) to achieve a steady state in nasal tissues. After 8 min of equilibration, impinger samples were collected, approximately every 4 min, for up to 40 min and analyzed for ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) and acetaldehyde by gas chromatography ... Acetaldehyde was found in expired air at all ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) exposure concentrations. With increasing the ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) exposure, concentration of acetaldehyde in expired air increased. At ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) exposure of approximately 1000 ppm the concentration of acetaldehyde in the expired air was 277 ppm (499 mg/cu m). Rats were administered oral doses of 14C-ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) (labeled at the vinyl moiety, 1 mL of a 10000 ppm (v/v) aqueous solution, overall dose level 297 mg/kg bw) by gastric intubation. The dosing regimen was 6 times 1 hour apart. During the dosing regime and subsequent 96 hr collection period, a mean of 64.4% of the administered radioactivity was excreted (1.4% in feces, 1.8% in urine and 61.2% in exhaled air). In addition a mean of 5.4% was found in the carcass at 96 hr. The major portion of the urinary radioactivity was excreted within the first 24 hr. Most of the radioactivity eliminated by the expired air was recovered during the 6 hr dosing regime and the first 6 hr after dosing. This portion of radioactivity was recovered from the traps designed for collecting carbon dioxide. The authors of the study suppose, that the unaccounted 30.1% of the dose were most likely lost in the expired air, which escaped from the metabolism cages when the animals were removed for dosing. There was a wide tissue distribution of radioactivity following administration of 14C-ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) by the oral route. One hour after the sixth dose the highest mean concentrations of radioactivity were found in the harderian gland and the submaxillary salivary gland. High levels were also found in the liver, kidney, stomach, ileum, colon and gastrointestinal tract contents. Low concentrations of radioactivity were found in fat. Attempts have been undertaken to determine ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) metabolites in urine and feces. No radiolabeled carbonates or bicarbonates were found in urine or feces. Thin layer chromatography of urine indicated that there was one major radioactive fraction and several minor fractions. Exhaled radioactivity was entirely present as 14C carbon dioxide. Therefore it can be concluded, that 63 % of orally applied 14C ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is excreted as metabolites. On/ hydrolysis /in the blood/, ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) yields acetic acid, a normal body constituent, and vinyl alcohol, which should rapidly tautomerize to yield acetaldehyde, another normal body constituent. The hydrolysis of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) was studied in vitro with rat liver and lung microsomes, rat and human plasma and purified esterases (acetylcholine esterase, butyrylcholine esterase, carboxyl esterase). Characterization of the kinetic parameters revealed that rat liver microsomes and purified carboxyl esterase (from porcine liver) displayed the highest activity. In order to establish the rate of metab of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) in vivo, rats were exposed in closed desiccator jar chambers, and gas uptake kinetics were studied. The decay of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) was dose-dependent, indicating possible satn of metabolic pathway(s). The maximal clearance (at lower concn) of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) from the system (30,000 mL/hr/kg) was similar to the maximal ventilation rate in this species. The exposure of rats to ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) resulted in a transient exhalation of significant amts of acetaldehyde into the closed exposure system. Gas chromatographic analysis of human whole-blood lymphocyte cultures treated for 10 seconds to 20 min with ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) (5.4 mM) revealed a rapid degradation of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) and formation of acetaldehyde. During the 20 min observation period, no degradation of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) or formation of acetaldehyde were observed in complete culture medium without blood, which suggested that the reaction was enzymatic. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) hydrolysis has been studied in vitro in the oral mucosal tissues from the oral cavity of rats and mice. The hydrolysis activity of the oral tissues is at least 100-fold lower than that of the nasal tissues. A physiologically based pharmacokinetic model was developed which describes the deposition of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) in the nasal cavity of the rat. This model predicts steady state concentrations of the metabolite acetic acid after continuing 6 hr-exposure in respiratory tissue which are approximately 13 times greater and in olfactory tissue which are approximately 2 times greater than those of acetaldehyde, the second metabolite. As the concentration of acids is indicative for the concentration of protons the model predicts the greatest reduction in intracellular pHi for respiratory mucosa. Hence, pH effects should be more pronounced in this tissue as compared to other tissues. This physiologically based toxicokinetic/toxicodynamic model for rat was modified for the olfactory epithelium of the both human and rat nasal cavity. The change in intracellular pH is predicted to be slightly greater for human olfactory epithelium, than that of rats. To provide validation data for this model, controlled human exposures at exposure levels of 1, 5 and 10 ppm to inhaled ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) were conducted. Air was sampled by a probe inserted into the nasopharyngeal cavity of five volunteers at bi-directional breathing through the nose. Data from ion trap mass spectrometry measurements of labeled ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) and acetaldehyde were compared with data from the human nasal model simulation. For the ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) data a good fit was demonstrated (r = 0.9). The metabolism of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) has been studied in animals ... ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is rapidly hydrolyzed by esterases in the blood to acetate and the unstable intermediate, vinyl alcohol. Vinyl alcohol is rapidly converted to acetaldehyde, which in turn is metabolized to acetate in the liver. This in turn is incorporated into the "2 carbon pool" of normal body metabolism and eventually forms CO2 as the major breakdown product. Therefore, the metabolism of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) results in two acetate molecules that enter the 2 carbon pool. This has been confirmed in excretion studies that have documented 14CO2 in exhaled air as the major metabolite and source of radioactivity recovered following either inhalation or oral exposure to 14C-VA. A very small amount also appears to be excreted in the urine as urea and several other unidentified metabolites. The metabolic pattern was not influenced by the route of administration. Similar results were found in rats exposed to concentrations of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) (200-2,000 ppm) in the air for 1.4 hours or less. The results show that ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is rapidly metabolized by blood esterases and that hepatic monooxygenases have a minor role, if any, in the metabolism of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM). In vitro metabolic studies show that ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) added to preparations of rat liver supernatant did conjugate (although not to a large degree) with glutathione. The reaction is mediated by glutathione S-transferase and further metabolism produces mercapturic acid derivatives that are eliminated in the urine. Rats exposed for 5 hours a day for 6 months to ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) in the air (10, 100, or 500 mg/cu m) showed a significant depletion of free non-protein thiols in the liver but not in a dose-dependent pattern. According to the authors, the thiol depletion indicates that conjugation with glutathione plays an important role in the detoxification of this chemical. Similar results were seen in rats, guinea pigs, and mice given single intraperitoneal doses of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM). The highest decrease (50%) in SH content was seen in guinea pigs following a single intraperitoneal injection of 500 mg/kg ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM). Glutathione conjugation may decrease the toxicity of potentially harmful electrophiles by facilitating excretion into the bile. These studies show that ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) quickly undergoes hydrolysis in the body through several intermediate steps to form the principal end products, carbon dioxide and water. The metabolic pattern was not influenced by the route of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) exposure, but did show nonlinear kinetic patterns at high concentrations, indicating that the metabolic processes are saturable. In vivo and in vitro tests indicate that ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) may bind to various degrees with glutathione in different species, which may help to detoxify ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) or its metabolites and enhance their elimination. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is hydrolyzed by carboxylesterases to acetic acid and acetaldehyde which is subsequently oxidized to acetic acid by aldehyde dehydrogenases. Acetate enters the citric cycle in an activated form as acetyl coenzyme A. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) metabolism not only takes place in the liver but also in several tissues. The half-life of /200 uM/ ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) elimination in human whole blood was 4.1 minutes as compared to /less than/ 1 minute in rat whole blood. Acetaldehyde is a metabolite of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) through esterase-mediated metabolism. It is discussed that ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) exhibits its genotoxicity via acetaldehyde. For example /researchers/ demonstrated that ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) induces /DNA protein crosslinking/ via acetaldehyde, and ... chromosomal damage induced by ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) in mammalian cell cultures is through formation of acetaldehyde ... Acetaldehyde is a naturally occurring substance in the metabolic pathways of animals and humans (metabolism of ethanol and sugars). It occurs in small quantities in human blood. Therefore, it may well be that acetaldehyde expresses its genotoxic potential in case of metabolic overload. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is primarily used as a monomer in the production of polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) and polyvinyl alcohol. Its chief use is as a monomer for making poly(ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM)) and ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) copolymers, which are used as components in coatings, paints, and sealants, binders (adhesives, nonwovens, construction products, and carpet-backing) and in miscellaneous uses such as chewing gum and tablet coatings. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is also copolymerized as the minor constituent with vinyl chloride and with ethylene to form commercial polymers and with acrylonitrile to form acrylic fibers. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) has been used primarily to produce polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) emulsions and polyvinyl alcohol. The principle use of these emulsions has been in adhesives, paints, textiles, and paper products. PRODUCT PROFILE: ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM): PolyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) accounts for about 48% of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) monomer (VAM) use, with applications including water-based paints, adhesives, acrylic fibres, paper coatings or non-woven binders. Polyvinyl alcohol (PVOH), used in packaging film and glass laminates, accounts for about 35% of demand. The remainder goes into ethylene ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) (EVA) polymers, ethylene vinyl alcohol (EVOH) barrier resins. PRODUCT PROFILE: ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM): ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) monomer's (VAM) main use is polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) which accounts for about 47% of consumption and has applications in water-based paints, adhesives, acrylic fibres, paper coatings or non-woven binders. Polyvinyl alcohol (PVOH), which is used in packaging film and glass laminates, accounts for about 29% of VAM demand. Remaining volumes go into ethylene ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) (EVA) polymers, ethylene vinyl alcohol (EVOH) barrier resins and polyvinyl butyral (PVB). EVA and EVOH are finding new uses as copolymers in speciality adhesives and packaging films. CHEMICAL PROFILE: ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM): ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) monomer (VAM) is mainly used in polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) which has applications in water-based paints, adhesives, acrylic fibres, paper coatings and non-woven binders. Polyvinyl alcohol (PVOH), used in packaging film and glass laminates, is the second largest consumer. The remaining volumes go into ethylene ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) (EVA) polymers, ethylene vinyl alcohol (EVOH) barrier resins and polyvinyl butyral (PVB). CHEMICAL PROFILE: ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM). PolyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) emulsions and resins, 40%; (this area is divided evenly between paints and adhesives); polyvinyl alcohol, 15%; polyvinyl butyral, 8%; ethylene-ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) resins, 6%; polyvinyl chloride copolymers, 3%; miscellaneous, 1%; exports, 27%. CHEMICAL PROFILE: ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM): PolyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) emulsions and resins, 57%; polyvinyl alcohol, 19%; polyvinyl butyral, 10%; ethylene-ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) resins, 8%; ethylene vinyl alcohol, 2%; miscellaneous, including polyvinyl chloride copolymers, 4%. PRODUCT FOCUS: ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) Monomer (VAM): Global Demand: 2003: 4.3 million tonnes. PolyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM), 44%; polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM), 40%; ethylene vinyl alcohol, 12%. PRODUCT FOCUS: ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) Monomer (VAM): Global Demand: 2006: 4.8 million tonnes. PolyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM), 43%; polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM), 42%; ethylene-ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) copolymers, 9%; Other, 6%. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM), acetic anhydride, ethanol, methanol, and formaldehyde were formed in aq extracts of polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) films only in some cases and in insignificant quantities. The difference between pH of aq extracts of polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) films and pH of the control (distilled water) the extracts from unsterilized films are more alk and those from sterilized films are more acidic than the distilled water control. Bromo cmpd were present up to 6.4 mg bromide/L in polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) film extracts and up to 12.3 mg bromide/L in inactivated extracts. The oxidizability of the polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) films was around 324-1310 mg/L and was highly dependent on the time of contact of the films with water. Aq extracts of various films contained 80-360 mg/L polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM). Sterilization by gamma-rays did not lead to substantial changes in hygienic-chem properties of the films. An increase in the irradiation dose up to 0.3 megagray decreased the oxidizability of aq extracts and the polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) content in the films. The quantities of formaldehyde and methanol formed are lower than the accepted quantities of migration of these substances into food products. Thus, polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) has satisfactory properties for medicinal use. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is an industrial chemical that is produced in large amounts in the United States. It is a clear, colorless liquid with a sweet, fruity smell. It is very flammable and may be ignited by heat, sparks, or flames. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is used to make other industrial chemicals. These chemicals are used mainly to make glues for the packaging and building industries. They are also used to make paints, textiles, and paper. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is also used as a coating in plastic films for food packaging and as a modifier of food starch. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is primarily used as a monomer in the production of polyORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) and polyvinyl alcohol. Acute (short-term) inhalation exposure of workers to ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) has resulted in eye irritation and upper respiratory tract irritation. Chronic (long-term) occupational exposure did not result in any severe adverse effects in workers; some instances of upper respiratory tract irritation, cough, and/or hoarseness were reported. Nasal epithelial lesions and irritation and inflammation of the respiratory tract were observed in mice and rats chronically exposed by inhalation. No information is available on the reproductive, developmental, or carcinogenic effects of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) in humans. An increased incidence of nasal cavity tumors has been observed in rats exposed by inhalation. In one drinking water study, an increased incidence of tumors was reported in rats. EPA has not classified ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) for carcinogenicity. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) shall be stored at temperatures less than 37.8 °C (100 °F) in well-ventilated areas and kept away from ignition sources such as heat and direct sunlight. No heating apparatus capable of exceeding 80% of the autoignition temperature of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) (427 °C) shall be used in ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) storage areas. The storage of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) in glass containers should not be in the same areas as oxidizing agents or other incompatible chemicals. Containers of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) shall be kept tightly closed when not in use and shall be stored so as to minimize accidental ruptures and spills. Evaluation: There is inadequate evidence in humans for the carcinogenicity of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM). There is limited evidence in experimental animals for the carcinogenicity of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM). Overall evaluation: ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is possibly carcinogenic to humans (Group 2B). In making the overall evaluation, the working group took into account the following evidence: (1) ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) is rapidly transformed into acetaldehyde in human blood and animal tissues. (2) There is sufficient evidence in experimental animals for the carcinogenicity of acetaldehyde. Both ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) and acetaldehyde induce nasal cancer in rats after administration by inhalation. (3) ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) and acetaldehyde are genotoxic in human cells in vitro and on animals in vivo. Previous studies from our laboratory suggest that rat liver microsome-activated ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) induces plasmid DNA-histone crosslinks, in vitro, through esterase-mediated metabolism. Since nasal tissues contain high levels of carboxylesterase, tumorigenesis may be related to in situ production of the hydrolysis products acetaldehyde and acetic acid. ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) was cytotoxic to both respiratory and olfactory tissues in vitro at 50-200 mM, but not 25 mM, after 2 hr exposure. Pretreatment of rats with the carboxylesterase inhibitor, bis-(p-nitrophenyl) phosphate (BNPP), attenuated the cytotoxic effects and metabolism of ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM) in both tissue types. Semicarbazide, an aldehyde scavenger, was unable to protect the tissues from ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Asetat, VAM)-induced cytotoxicity. When the metabolites were tested, acetic acid, but not acetaldehyde, was cytotoxic to both tissues. To provide validation data for the application of the PBPK model ... in humans, controlled human exposures to inhaled ORP HYDROFLEX 64 (Vinyl Acetate, Vinil Aset
ORP THERMOBOND 65
ORP THERMOBOND 65 ORP Thermobond 65 is a redispersible powder produced by drying an emulsion of Vinyl Acetate / Vinyl Versatate / Acrylic terpolymer with PVOH as protective colloid. The specific chemical composition of the polymer allows coalescence of the redispersed polymer at low temperatures and provides good adhesion on mineral substrates. ORP Thermobond 65 is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP Thermobond 65 improves adhesion, flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially because of the flexible nature ORP Thermobond 65 performs very well in transverse deformation conditions. TYPICAL PROPERTIES Appearance White powder Chemical composition VA / VV / Acrylic Terpolymer Stabilizing System PVOH Residual Humidity (%) Max. 2.0 Bulk Density (g/l) 400 - 600 Ash Content (%) 12 ± 2 Alkali Resistance High After 1:1 Dispersion with Water MFFT (°C) 0 ±1 APPLICATION AREAS ORP Thermobond 65 can be used in mortar formulations where good flexibility/elasticity, recovery and thixotropic behavior is required. ETICS (Exterior Thermal Insulation Coating Systems) Plasters: Due to its excellent flexibility and water resistance, ORP Thermobond 65 can be used for manufacturing of cementitious base coats applied on EPS&XPS boards in ETICS. The recommended dosage: 3.0 – 5.0 % Adhesives for EPS&XPS boards in ETICS: The recommended dosages: 1.0 – 2.0 % Tile Adhesives (S1 & S2): The recommended dosages: 3.0 – 7.0 % PRODUCT HANDLING – STORAGE – SHELFLIFE Packaging: Pallet with 18 paper bags, each 25 kg, also 500 or 1000 kg of big bags. Packages must be stored in a dry and cool warehouse. Pallets must not be stacked on top of each other to avoid caking due to the thermoplasticity of the polymer. Packing must be closed well after usage for protection against humidity and caking. It has to be used within 6 months after the date of delivery. ORP THERMOBOND 65 is a redispersible powder produced by drying an emulsion of Vinyl Acetate / Acrylic copolymer with PVOH as protective colloid. The specific chemical composition of the polymer allows coalescence of the redispersed polymer at low temperatures and provides good adhesion to cementitious substrates. ORP THERMOBOND 65 is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP THERMOBOND 65 improves adhesion, flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially in self levelling mortar formulations ORP THERMOBOND 65 provides excellent abrasion resistance, flexural & compressive stength and good leveling. APPLICATION AREAS of ORP THERMOBOND 65 ORP THERMOBOND 65 can be used between 1.5 – 4.0 % in self leveling mortar formulations. This amount of usage provides high abrasion resistance, water resistance, flexural & compressive strength. Also decreases segmentation and efflorescence. PRODUCT HANDLING – STORAGE – SHELFLIFE of ORP THERMOBOND 65 Packaging: Pallet with 18 paper bags, each 25 kg, also 500 or 1000 kg of big bags. Packages must be stored in a dry and cool warehouse. Pallets must not be stacked on top of each other to avoid caking due to the thermoplasticity of the polymer. Packing must be closed well after usage for protection against humidity and caking. ORP THERMOBOND 65 has to be used within 6 months after the date of delivery. ORP THERMOBOND 65 is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP THERMOBOND 65 improves adhesion, flexibility, hydrophobicity and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially because of the flexible nature, ORP THERMOBOND 65 performs very well in transverse deformation conditions. APPLICATION AREAS of ORP THERMOBOND 65 ORP THERMOBOND 65 can be used in mortar formulations where highly flexbily/elastic, hydrophobic and water resistant behavior is required at the same time. In high performance of ceramic tile grouts formulations (CG2) ORP THERMOBOND 65 can be used with the ratio of 2.0 - 4.0 % in weight and without requiring an additional hydrophobic agent. Moreover ORP THERMOBOND 65 is a very suitable redispersible powder polymer for cementitious water proofing mortars.It can be used with the ratio of 7.0 - 12.0 % in weight in 1K cementitious water proofing mortar formulations. Because of its molecular structure it provides high crack bridging ability. Also ORP THERMOBOND 65 performs very well in cementitious exterior plasters and topcoats with the amunt of 2.0 - 4.0 %. PRODUCT HANDLING - STORAGE - SHELFLIFE of ORP THERMOBOND 65 Packaging: Pallet with 18 paper bags, each 25 kg, also 500 or 1000 kg of big bags. Packages must be stored in a dry and cool warehouse. Pallets must not be stacked on top of each other to avoid caking due to the thermoplasticity of the polymer. Packing must be closed well after usage for protection against humidity and caking. It has to be used within 6 months after the date of delivery. 1.Product identifier Product name ORP THERMOBOND 65 Chemical name and synonym Vinyl Acetate l VeoVa l Acrylic terpolymer 2.Relevant identified uses of the substance or mixture and uses advised against Intended use Redispersible Powder for Dry-Mix Mortars The product does not contain substances classified as being hazardous to human health or the environment pursuant to the provisions Regulation (EU) 1272/2008 (CLP) (and subsequent amendments and supplements) in such quantities as to require the statement. ORP THERMOBOND 65 can be released to the environment from industrial sources and biomass combustion(1). Waste gases from scrubbers (generated during the industrial manufacture of ORP THERMOBOND 65 ) may contain trace levels of ORP THERMOBOND 65 (2). An emission factor of 6.22 ug/g ORP THERMOBOND 65 from extruded ethylene-ORP THERMOBOND 65 and ORP THERMOBOND 65 copolymer (28% ORP THERMOBOND 65 ) was determined experimentally at 435 °C under laboratory conditions. All low density polyethylene and ethylene-methyl acrylate copolymers with ORP THERMOBOND 65 emitted >0.01 ug/g ORP THERMOBOND 65 at 435 °C(3). How is it produced? The main production method for ORP THERMOBOND 65 monomer is the reaction of ethylene and acetic acid with oxygen, in the presence of a palladium catalyst. The ORP THERMOBOND 65 is recovered by condensation and scrubbing and is then purified by distillation. A new manufacturing process, dubbed Leap, could offer large capital cost savings as a more efficient fluidised bed system replaces the fixed bed reactors currently in use. The oldest means of manufacturing ORP THERMOBOND 65 is the addition of acetic acid to acetylene and this process is still used but not on a large scale. How is it stored and distributed? ORP THERMOBOND 65 monomer is stored in mild steel storage tanks and/or new or reconditioned steel drums and can be transported by bulk vessels or tank trucks. It has a specific gravity of 0.933 and a flash point of -8° C (closed cup) and is highly flammable. It should therefore be stored in a cool, dry, well-ventilated area that is free from the risk of ignition. For transportation purposes, it is classified as packing group II and hazard class 3 and it is an irritant. What is ORP THERMOBOND 65 Monomer used for? ORP THERMOBOND 65 monomer is mainly used in the production of polyORP THERMOBOND 65 (PVAc) and polyvinyl alcohol (PVOH or PVA). In fact, 80 % of all the ORP THERMOBOND 65 produced in the world is used to make these two chemicals. PolyORP THERMOBOND 65 is used in paints, adhesives, paper coatings and textile treatments, while polyvinyl alcohol is used in the production of adhesives, coatings, and water soluble packaging, and textile warp sizing. ORP THERMOBOND 65 is also used to make polyvinyl butyral (PVB) which is used in laminated safety glass for cars and buildings. Ethylene-ORP THERMOBOND 65 (EVA) resin is also made from ORP THERMOBOND 65 and is used in the manufacture of packaging film, heavy-duty bags, extrusion coating, wire and cable jacketing, hot-melt adhesives and cross-linked foam. Other products made from ORP THERMOBOND 65 are ethylene-vinyl alcohol (EVOH) resins which are used as a gas barrier in multi-layered food and beverage packages, and as a barrier layer in automobile tanks. Production of ORP THERMOBOND 65 The worldwide production capacity of ORP THERMOBOND 65 was estimated at 6,969,000 tonnes/year in 2007, with most capacity concentrated in the United States (1,585,000 all in Texas), China (1,261,000), Japan (725,000) and Taiwan (650,000).[4] The average list price for 2008 was $1600/tonne. Celanese is the largest producer (ca 25% of the worldwide capacity), while other significant producers include China Petrochemical Corporation (7%), Chang Chun Group (6%), and LyondellBasell (5%).[4] It is a key ingredient in furniture glue.[5] Preparation ORP THERMOBOND 65 is the acetate ester of vinyl alcohol. Since vinyl alcohol is highly unstable (with respect to acetaldehyde), the preparation of ORP THERMOBOND 65 is more complex than the synthesis of other acetate esters. The major industrial route involves the reaction of ethylene and acetic acid with oxygen in the presence of a palladium catalyst.[6] {\displaystyle {\ce {2 C2H4 + 2 CH3CO2H + O2 -> 2 CH3CO2CHCH2 + 2 H2O}}}{\displaystyle {\ce {2 C2H4 + 2 CH3CO2H + O2 -> 2 CH3CO2CHCH2 + 2 H2O}}} The main side reaction is the combustion of organic precursors. Mechanism Isotope labeling and kinetics experiments suggest that the mechanism involves PdCH2CH2OAc-containing intermediates. Beta-hydride elimination would generate ORP THERMOBOND 65 and a palladium hydride, which would be oxidized to give hydroxide. Polymerization It can be polymerized to give polyORP THERMOBOND 65 (PVA). With other monomers it can be used to prepare various copolymers such as ethylene-ORP THERMOBOND 65 (EVA), ORP THERMOBOND 65 -acrylic acid (VA/AA), polyvinyl chloride acetate (PVCA), and polyvinylpyrrolidone (Vp/Va Copolymer, used in hair gels).[8] Due to the instability of the radical, attempts to control the polymerization via most 'living/controlled' radical processes have proved problematic. However, RAFT (or more specifically MADIX) polymerization offers a convenient method of controlling the synthesis of PVA by the addition of a xanthate or a dithiocarbamate chain transfer agent. Other reactions ORP THERMOBOND 65 undergoes many of the reactions anticipated for an alkene and an ester. Bromine adds to give the dibromide. Hydrogen halides add to give 1-haloethyl acetates, which cannot be generated by other methods because of the non-availability of the corresponding halo-alcohols. Acetic acid adds in the presence of palladium catalysts to give ethylidene diacetate, CH3CH(OAc)2. It undergoes transesterification with a variety of carboxylic acids.[9] The alkene also undergoes Diels-Alder and 2+2 cycloadditions. ORP THERMOBOND 65 undergoes transesterification, giving access to vinyl ethers: ROH + CH2=CHOAc → ROCH=CH2 + HOAc Toxicity evaluation Tests suggest that ORP THERMOBOND 65 is of low toxicity. For rats (oral) LD50 is 2920 mg/kg.[3] On January 31, 2009, the Government of Canada's final assessment concluded that exposure to ORP THERMOBOND 65 is not harmful to human health.[12] This decision under the Canadian Environmental Protection Act (CEPA) was based on new information received during the public comment period, as well as more recent information from the risk assessment conducted by the European Union. It is classified as an extremely hazardous substance in the United States as defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. 11002), and is subject to strict reporting requirements by facilities which produce, store, or use it in significant quantities. ORP THERMOBOND 65 appears as a clear colorless liquid. Flash point 18°F. Density 7.8 lb / gal. Slightly soluble in water. Vapors are heavier than air. Vapors irritate the eyes and respiratory system. May polymerize if heated or contaminated. If polymerization occurs inside a container, the container may violently rupture. Used to make adhesives, paints, and plastics. At 20 °C, a saturated solution of ORP THERMOBOND 65 in water contains 2.0-2.4 wt % ORP THERMOBOND 65 , whereas a saturated solution of water in ORP THERMOBOND 65 contains 0.9-1.0 wt % water; at 50 °C, the solubility of ORP THERMOBOND 65 in water is 0.1 wt % more than at 20 °C, but the solubility of water in ORP THERMOBOND 65 doubles to about 2 wt % The/ fate of inhaled ORP THERMOBOND 65 in rabbits /was studied/. ... ORP THERMOBOND 65 tended to remain in the body after it was inhaled; 70% of the ORP THERMOBOND 65 administered was retained, and an equilibrium was established in the first few min after exposure began. ... No ORP THERMOBOND 65 /was found/ in the blood, either during or after its inhalation, which suggested ... that ORP THERMOBOND 65 is rapidly metabolized when it enters the body through the lungs. Two male Wistar Rats exposed to ORP THERMOBOND 65 (stabilized with 0.01% hydroquinone) concentrations varying between 200 and 2000 ppm in closed chambers with an exposure time of 1.4 hr or less demonstrated dose dependent elimination kinetics. The authors concluded that the metabolic pathways became saturated when ORP THERMOBOND 65 exposure levels exceeded 650 ppm (2320 mg/cu m). ORP THERMOBOND 65 deposition was measured in the isolated upper respiratory tract (URT) of anaesthetized adult male CrlCD:BR rats at exposure concentrations ranging from 73 to 2190 ppm during 1 hr inhalation under unidirectional flow conditions (flow rate 100 mL/min) ... Preliminary experiments showed that approximately 8 min of exposure was required for ORP THERMOBOND 65 to achieve a steady state in nasal tissues. After 8 min of equilibration, impinger samples were collected, approximately every 4 min, for up to 40 min and analyzed for ORP THERMOBOND 65 and acetaldehyde by gas chromatography ... Acetaldehyde was found in expired air at all ORP THERMOBOND 65 exposure concentrations. With increasing the ORP THERMOBOND 65 exposure, concentration of acetaldehyde in expired air increased. At ORP THERMOBOND 65 exposure of approximately 1000 ppm the concentration of acetaldehyde in the expired air was 277 ppm (499 mg/cu m). Rats were administered oral doses of 14C-ORP THERMOBOND 65 (labeled at the vinyl moiety, 1 mL of a 10000 ppm (v/v) aqueous solution, overall dose level 297 mg/kg bw) by gastric intubation. The dosing regimen was 6 times 1 hour apart. During the dosing regime and subsequent 96 hr collection period, a mean of 64.4% of the administered radioactivity was excreted (1.4% in feces, 1.8% in urine and 61.2% in exhaled air). In addition a mean of 5.4% was found in the carcass at 96 hr. The major portion of the urinary radioactivity was excreted within the first 24 hr. Most of the radioactivity eliminated by the expired air was recovered during the 6 hr dosing regime and the first 6 hr after dosing. This portion of radioactivity was recovered from the traps designed for collecting carbon dioxide. The authors of the study suppose, that the unaccounted 30.1% of the dose were most likely lost in the expired air, which escaped from the metabolism cages when the animals were removed for dosing. There was a wide tissue distribution of radioactivity following administration of 14C-ORP THERMOBOND 65 by the oral route. One hour after the sixth dose the highest mean concentrations of radioactivity were found in the harderian gland and the submaxillary salivary gland. High levels were also found in the liver, kidney, stomach, ileum, colon and gastrointestinal tract contents. Low concentrations of radioactivity were found in fat. Attempts have been undertaken to determine ORP THERMOBOND 65 metabolites in urine and feces. No radiolabeled carbonates or bicarbonates were found in urine or feces. Thin layer chromatography of urine indicated that there was one major radioactive fraction and several minor fractions. Exhaled radioactivity was entirely present as 14C carbon dioxide. Therefore it can be concluded, that 63 % of orally applied 14C ORP THERMOBOND 65 is excreted as metabolites. On/ hydrolysis /in the blood/, ORP THERMOBOND 65 yields acetic acid, a normal body constituent, and vinyl alcohol, which should rapidly tautomerize to yield acetaldehyde, another normal body constituent. The hydrolysis of ORP THERMOBOND 65 was studied in vitro with rat liver and lung microsomes, rat and human plasma and purified esterases (acetylcholine esterase, butyrylcholine esterase, carboxyl esterase). Characterization of the kinetic parameters revealed that rat liver microsomes and purified carboxyl esterase (from porcine liver) displayed the highest activity. In order to establish the rate of metab of ORP THERMOBOND 65 in vivo, rats were exposed in closed desiccator jar chambers, and gas uptake kinetics were studied. The decay of ORP THERMOBOND 65 was dose-dependent, indicating possible satn of metabolic pathway(s). The maximal clearance (at lower concn) of ORP THERMOBOND 65 from the system (30,000 mL/hr/kg) was similar to the maximal ventilation rate in this species. The exposure of rats to ORP THERMOBOND 65 resulted in a transient exhalation of significant amts of acetaldehyde into the closed exposure system. Gas chromatographic analysis of human whole-blood lymphocyte cultures treated for 10 seconds to 20 min with ORP THERMOBOND 65 (5.4 mM) revealed a rapid degradation of ORP THERMOBOND 65 and formation of acetaldehyde. During the 20 min observation period, no degradation of ORP THERMOBOND 65 or formation of acetaldehyde were observed in complete culture medium without blood, which suggested that the reaction was enzymatic. ORP THERMOBOND 65 hydrolysis has been studied in vitro in the oral mucosal tissues from the oral cavity of rats and mice. The hydrolysis activity of the oral tissues is at least 100-fold lower than that of the nasal tissues. A physiologically based pharmacokinetic model was developed which describes the deposition of ORP THERMOBOND 65 in the nasal cavity of the rat. This model predicts steady state concentrations of the metabolite acetic acid after continuing 6 hr-exposure in respiratory tissue which are approximately 13 times greater and in olfactory tissue which are approximately 2 times greater than those of acetaldehyde, the second metabolite. As the concentration of acids is indicative for the concentration of protons the model predicts the greatest reduction in intracellular pHi for respiratory mucosa. Hence, pH effects should be more pronounced in this tissue as compared to other tissues. This physiologically based toxicokinetic/toxicodynamic model for rat was modified for the olfactory epithelium of the both human and rat nasal cavity. The change in intracellular pH is predicted to be slightly greater for human olfactory epithelium, than that of rats. To provide validation data for this model, controlled human exposures at exposure levels of 1, 5 and 10 ppm to inhaled ORP THERMOBOND 65 were conducted. Air was sampled by a probe inserted into the nasopharyngeal cavity of five volunteers at bi-directional breathing through the nose. Data from ion trap mass spectrometry measurements of labeled ORP THERMOBOND 65 and acetaldehyde were compared with data from the human nasal model simulation. For the ORP THERMOBOND 65 data a good fit was demonstrated (r = 0.9). The metabolism of ORP THERMOBOND 65 has been studied in animals ... ORP THERMOBOND 65 is rapidly hydrolyzed by esterases in the blood to acetate and the unstable intermediate, vinyl alcohol. Vinyl alcohol is rapidly converted to acetaldehyde, which in turn is metabolized to acetate in the liver. This in turn is incorporated into the "2 carbon pool" of normal body metabolism and eventually forms CO2 as the major breakdown product. Therefore, the metabolism of ORP THERMOBOND 65 results in two acetate molecules that enter the 2 carbon pool. This has been confirmed in excretion studies that have documented 14CO2 in exhaled air as the major metabolite and source of radioactivity recovered following either inhalation or oral exposure to 14C-VA. A very small amount also appears to be excreted in the urine as urea and several other unidentified metabolites. The metabolic pattern was not influenced by the route of administration. Similar results were found in rats exposed to concentrations of ORP THERMOBOND 65 (200-2,000 ppm) in the air for 1.4 hours or less. The results show that ORP THERMOBOND 65 is rapidly metabolized by blood esterases and that hepatic monooxygenases have a minor role, if any, in the metabolism of ORP THERMOBOND 65. In vitro metabolic studies show that ORP THERMOBOND 65 added to preparations of rat liver supernatant did conjugate (although not to a large degree) with glutathione. The reaction is mediated by glutathione S-transferase and further metabolism produces mercapturic acid derivatives that are eliminated in the urine. Rats exposed for 5 hours a day for 6 months to ORP THERMOBOND 65 in the air (10, 100, or 500 mg/cu m) showed a significant depletion of free non-protein thiols in the liver but not in a dose-dependent pattern. According to the authors, the thiol depletion indicates that conjugation with glutathione plays an important role in the detoxification of this chemical. Similar results were seen in rats, guinea pigs, and mice given single intraperitoneal doses of ORP THERMOBOND 65 . The highest decrease (50%) in SH content was seen in guinea pigs following a single intraperitoneal injection of 500 mg/kg ORP THERMOBOND 65 . Glutathione conjugation may decrease the toxicity of potentially harmful electrophiles by facilitating excretion into the bile. These studies show that ORP THERMOBOND 65 quickly undergoes hydrolysis in the body through several intermediate steps to form the principal end products, carbon dioxide and water. The metabolic pattern was not influenced by the route of ORP THERMOBOND 65 exposure, but did show nonlinear kinetic patterns at high concentrations, indicating that the metabolic processes are saturable. In vivo and in vitro tests indicate that ORP THERMOBOND 65 may bind to various degrees with glutathione in different species, which may help to detoxify ORP THERMOBOND 65 or its metabolites and enhance their elimination. ORP THERMOBOND 65 is hydrolyzed by carboxylesterases to acetic acid and acetaldehyde which is subsequently oxidized to acetic acid by aldehyde dehydrogenases. Acetate enters the citric cycle in an activated form as acetyl coenzyme A. ORP THERMOBOND 65 metabolism not only takes place in the liver but also in several tissues. The half-life of /200 uM/ ORP THERMOBOND 65 elimination in human whole blood was 4.1 minutes as compared to /less than/ 1 minute in rat whole blood. Acetaldehyde is a metabolite of ORP THERMOBOND 65 through esterase-mediated metabolism. It is discussed that ORP THERMOBOND 65 exhibits its genotoxicity via acetaldehyde. For example /researchers/ demonstrated that ORP THERMOBOND 65 induces /DNA protein crosslinking/ via acetaldehyde, and ... chromosomal damage induced by ORP THERMOBOND 65 in mammalian cell cultures is through formation of acetaldehyde ... Acetaldehyde is a naturally occurring substance in the metabolic pathways of animals and humans (metabolism of ethanol and sugars). It occurs in small quantities in human blood. Therefore, it may well be that acetaldehyde expresses its genotoxic potential in case of metabolic overload. ORP THERMOBOND 65 is primarily used as a monomer in the production of polyORP THERMOBOND 65 and polyvinyl alcohol. Its chief use is as a monomer for making poly(ORP THERMOBOND 65 ) and ORP THERMOBOND 65 copolymers, which are used as components in coatings, paints, and sealants, binders (adhesives, nonwovens, construction products, and carpet-backing) and in miscellaneous uses such as chewing gum and tablet coatings. ORP THERMOBOND 65 is also copolymerized as the minor constituent with vinyl chloride and with ethylene to form commercial polymers and with acrylonitrile to form acrylic fibers. ORP THERMOBOND 65 has been used primarily to produce polyORP THERMOBOND 65 emulsions and polyvinyl alcohol. The principle use of these emulsions has been in adhesives, paints, textiles, and paper products. PRODUCT PROFILE: ORP THERMOBOND 65 : PolyORP THERMOBOND 65 accounts for about 48% of ORP THERMOBOND 65 monomer (VAM) use, with applications including water-based paints, adhesives, acrylic fibres, paper coatings or non-woven binders. Polyvinyl alcohol (PVOH), used in packaging film and glass laminates, accounts for about 35% of demand. The remainder goes into ethylene ORP THERMOBOND 65 (EVA) polymers, ethylene vinyl alcohol (EVOH) barrier resins. PRODUCT PROFILE: ORP THERMOBOND 65 : ORP THERMOBOND 65 monomer's (VAM) main use is polyORP THERMOBOND 65 which accounts for about 47% of consumption and has applications in water-based paints, adhesives, acrylic fibres, paper coatings or non-woven binders. Polyvinyl alcohol (PVOH), which is used in packaging film and glass laminates, accounts for about 29% of VAM demand. Remaining volumes go into ethylene ORP THERMOBOND 65 (EVA) polymers, ethylene vinyl alcohol (EVOH) barrier resins and polyvinyl butyral (PVB). EVA and EVOH are finding new uses as copolymers in speciality adhesives and packaging films. CHEMICAL PROFILE: ORP THERMOBOND 65 : ORP THERMOBOND 65 monomer (VAM) is mainly used in polyORP THERMOBOND 65 which has applications in water-based paints, adhesives, acrylic fibres, paper coatings and non-woven binders. Polyvinyl alcohol (PVOH), used in packaging film and glass laminates, is the second largest consumer. The remaining volumes go into ethylene ORP THERMOBOND 65 (EVA) polymers, ethylene vinyl alcohol (EVOH) barrier resins and polyvinyl butyral (PVB). CHEMICAL PROFILE: ORP THERMOBOND 65 . PolyORP THERMOBOND 65 emulsions and resins, 40%; (this area is divided evenly between paints and adhesives); polyvinyl alcohol, 15%; polyvinyl butyral, 8%; ethylene-ORP THERMOBOND 65 resins, 6%; polyvinyl chloride copolymers, 3%; miscellaneous, 1%; exports, 27%. CHEMICAL PROFILE: ORP THERMOBOND 65 : PolyORP THERMOBOND 65 emulsions and resins, 57%; polyvinyl alcohol, 19%; polyvinyl butyral, 10%; ethylene-ORP THERMOBOND 65 resins, 8%; ethylene vinyl alcohol, 2%; miscellaneous, including polyvinyl chloride copolymers, 4%. PRODUCT FOCUS: ORP THERMOBOND 65 Monomer (VAM): Global Demand: 2003: 4.3 million tonnes. PolyORP THERMOBOND 65 , 44%; polyORP THERMOBOND 65 , 40%; ethylene vinyl alcohol, 12%. ORP THERMOBOND 65 , acetic anhydride, ethanol, methanol, and formaldehyde were formed in aq extracts of polyORP THERMOBOND 65 films only in some cases and in insignificant quantities. The difference between pH of aq extracts of polyORP THERMOBOND 65 films and pH of the control (distilled water) the extracts from unsterilized films are more alk and those from sterilized films are more acidic than the distilled water control. Bromo cmpd were present up to 6.4 mg bromide/L in polyORP THERMOBOND 65 film extracts and up to 12.3 mg bromide/L in inactivated extracts. The oxidizability of the polyORP THERMOBOND 65 films was around 324-1310 mg/L and was highly dependent on the time of contact of the films with water. Aq extracts of various films contained 80-360 mg/L polyORP THERMOBOND 65 . Sterilization by gamma-rays did not lead to substantial changes in hygienic-chem properties of the films. An increase in the irradiation dose up to 0.3 megagray decreased the oxidizability of aq extracts and the polyORP THERMOBOND 65 content in the films. The quantities of formaldehyde and methanol formed are lower than the accepted quantities of migration of these substances into food products. Thus, polyORP THERMOBOND 65 has satisfactory properties for medicinal use. ORP THERMOBOND 65 is an industrial chemical that is produced in large amounts in the United States. It is a clear, colorless liquid with a sweet, fruity smell. It is very flammable and may be ignited by heat, sparks, or flames. ORP THERMOBOND 65 is used to make other industrial chemicals. These chemicals are used mainly to make glues for the packaging and building industries. They are also used to make paints, textiles, and paper. ORP THERMOBOND 65 is also used as a coating in plastic films for food packaging and as a modifier of food starch. ORP THERMOBOND 65 is primarily used as a monomer in the production of polyORP THERMOBOND 65 and polyvinyl alcohol. Acute (short-term) inhalation exposure of workers to ORP THERMOBOND 65 has resulted in eye irritation and upper respiratory tract irritation. Chronic (long-term) occupational exposure did not result in any severe adverse effects in workers; some instances of upper respiratory tract irritation, cough, and/or hoarseness were reported. Nasal epithelial lesions and irritation and inflammation of the respiratory tract were observed in mice and rats chronically exposed by inhalation. No information is available on the reproductive, developmental, or carcinogenic effects of ORP THERMOBOND 65 in humans. An increased incidence of nasal cavity tumors has been observed in rats exposed by inhalation. In one drinking water study, an increased incidence of tumors was reported in rats. EPA has not classified ORP THERMOBOND 65 for carcinogenicity. ORP THERMOBOND 65 shall be stored at temperatures less than 37.8 °C (100 °F) in well-ventilated areas and kept away from ignition sources such as heat and direct sunlight. No heating apparatus capable of exceeding 80% of the autoignition temperature of ORP THERMOBOND 65 (427 °C) shall be used in ORP THERMOBOND 65 storage areas. The storage of ORP THERMOBOND 65 in glass containers should not be in the same areas as oxidizing agents or other incompatible chemicals. Containers of ORP THERMOBOND 65 shall be kept tightly closed when not in use and shall be stored so as to minimize accidental ruptures and spills. Evaluation: There is inadequate evidence in humans for the carcinogenicity of ORP THERMOBOND 65 . There is limited evidence in experimental animals for the carcinogenicity of ORP THERMOBOND 65 . Overall evaluation: ORP THERMOBOND 65 is possibly carcinogenic to humans (Group 2B). In making the overall evaluation, the working group took into account the following evidence: (1) ORP THERMOBOND 65 is rapidly transformed into acetaldehyde in human blood and animal tissues. (2) There is sufficient evidence in experimental animals for the carcinogenicity of acetaldehyde. Both ORP THERMOBOND 65 and acetaldehyde induce nasal cancer in rats after administration by inhalation. (3) ORP THERMOBOND 65 and acetaldehyde are genotoxic in human cells in vitro and on animals in vivo. Previous studies from our laboratory suggest that rat liver microsome-activated ORP THERMOBOND 65 induces plasmid DNA-histone crosslinks, in vitro, through esterase-mediated metabolism. Since nasal tissues contain high levels of carboxylesterase, tumorigenesis may be related to in situ production of the hydrolysis products acetaldehyde and acetic acid. ORP THERMOBOND 65 was cytotoxic to both respiratory and olfactory tissues in vitro at 50-200 mM, but not 25 mM, after 2 hr exposure. Pretreatment of rats with the carboxylesterase inhibitor, bis-(p-nitrophenyl) phosphate (BNPP), attenuated the cytotoxic effects and metabolism of ORP THERMOBOND 65 in both tissue types. Semicarbazide, an aldehyde scavenger, was unable to protect the tissues from ORP THERMOBOND 65 -induced cytotoxicity. When the metabolites were tested, acetic acid, but not acetaldehyde, was cytotoxic to both tissues. To provide validation data for the application of the PBPK model ... in humans, controlled human exposures to inhaled ORP THERMOBOND 65 were conducted. Air was sampled by a probe inserted into the nasopharyngeal cavity of five volunteers (two women, three men). Volunteers were instructed to inhale and exhale through the nose. Sampling was carried out during exposure to labeled 13C1, 13C2-ORP THERMOBOND 65 during resting and light exercise at three exposure levels (1, 5 and 10 ppm nominally). Both, labeled ORP THERMOBOND 65 and the major metabolite acetaldehyde from the nasopharyngeal region were sampled at a calibrated flow rate of 12 L/hr and analyzed in real time utilizing ion trap mass spectrometry (MS/MS). Measurements were taken every 0.
ORP THERMOBOND 65
ORP Thermobond 65 is a Redispersible Powder for Dry-Mix Mortars INTRODUCTION ORP Thermobond 65 is a redispersible powder produced by drying an emulsion of Vinyl Acetate /Vinyl Versatate / Acrylic terpolymer with PVOH as protective colloid. The specific chemical composition of ORP Thermobond 65 allows coalescence of the redispersed polymer at low temperatures and provides good adhesion on mineral substrates. ORP Thermobond 65 is used to modify mixtures containing hydraulic binders. Due to its particular chemical and physical composition, ORP Thermobond 65 improves adhesion, flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially because of the flexible nature ORP Thermobond 65 performs very well in transverse deformation conditions. TYPICAL PROPERTIES Appearance: White powder Chemical composition: VA / VV / Acrylic Terpolymer Stabilizing System: PVOH Residual Humidity (%): Max. 2.0 Bulk Density (g/l): 400 - 600 Ash Content (%): 12 ± 2 Alkali Resistance: High After 1:1 Dispersion with Water MFFT: 0 ±1 APPLICATION AREAS ORP Thermobond 65 can be used in mortar formulations where good flexibility/elasticity, recovery and thixotropic behavior is required. ETICS (Exterior Thermal Insulation Coating Systems) Plasters: Due to its excellent flexibility and water resistance, ORP Thermobond 65 can be used for manufacturing of cementitious base coats applied on EPS&XPS boards in ETICS. The recommended dosage: 3.0 – 5.0 % Adhesives for EPS&XPS boards in ETICS: The recommended dosages: 1.0 – 2.0 % Tile Adhesives (S1 & S2): The recommended dosages: 3.0 – 7.0 % PRODUCT HANDLING – STORAGE – SHELFLIFE Packaging: Pallet with 18 paper bags, each 25 kg, also 500 or 1000 kg of big bags. Packages must be stored in a dry and cool warehouse. Pallets must not be stacked on top of each other to avoid caking due to the thermoplasticity of the polymer. Packing must be closed well after usage for protection against humidity and caking. ORP Thermobond 65 has to be used within 6 months after the date of delivery. Today, ATAMAN CHEMICALS supplies the market with polymer emulsions, redispersible powder polymers and specialty additives. Polymer Emulsions Offering a wide array of styrene, vinyl acetate and acrylic chemical compositions, ATAMAN CHEMICALS offers innovative solutions with various polymerization technologies for the cementitious and dispersion based construction chemicals markets. Redispersible Powder Polymers ATAMAN CHEMICALS provides solutions in carbon rich monomer combinations of vinyl versatate and acrylics that highlight properties such as water resistance, saponification resistance and flexibility. Specialty Additives Acrylic associative and non-associative rheology modifiers specifically are designed for fullfilling different application rheology requirements of different markets. Dispersion agents, both ammonia or sodium based salts, are able to work with different dispersing systems and chemistries. Rheology modifiers and dispersion agents are used in both dispersion based and liquid components of 2K Cementitious Systems. Technical Solution Partnership Approach of ATAMAN has dedicated synthesis and application laboratories within Research & Development Center With state of the art equipment, ATAMAN is able to perform all application and analysis tests in accordance with the regional and international standards Customer intimacy and solving customer needs is of utmost importance to ATAMAN; therefore, joint projects and testing for customers at the laboratories are executed with much diligence We distribute the following Organik Kimya products Orgal® Acrylate and styrene acrylate dispersions Orgal® Hydroflex Modified acrylate and styrene acrylate dispersions Orgal® Rooflex Modified acrylate and styrene acrylate dispersions Orgal® Vinyl acetate dispersions ORP® Redispersible dispersion powders ORP® Thermobond Redispersible dispersion powder for ETICS
ORP THERMOBOND 74
Introduction: ORP Thermobond 74 is a redispersible powder obtained by drying an emulsion of a vinyl acetate / acrylic copolymer with PVA as a protective colloid. The special chemical composition of the polymer facilitates the bonding of the redispersed polymer at low temperatures and ensures good adhesion to cementitious substrates. ORP Thermobond 74 is used to modify mixtures containing hydraulic binders. Thanks to its special chemical / physical composition, ORP Thermobond 74 improves the adhesion, elasticity and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially due to its flexible nature, ORP Thermobond 74 withstands lateral deformation tests very well. Properties: Appearance - White powder Chemical composition - Vinyl acetate / acrylic terpolymer Stabilizing system - PVA Residual moisture (%) - Max. 1.5 Density (g / l) - 400 - 600 Ash residue (%) - 14 ± 2 Alkaline resistance - High After dispersion with water - 1: 1 Minimum film formation temperature (° C ) - 0 Applications: ORP Thermobond 74 can be used in composition of mortars requiring good flexibility / elasticity, deformation resistance and thixotropic behavior. Plasters for external thermal insulation systems: Due to its excellent elasticity and water resistance, ORP Thermobond 74 can be used for the production of cement plaster used for boards of extruded polystyrene foam and expanded polystyrene in the external thermal insulation system. Recommended dosage: 3.0-5.0%. Adhesives for panels made of extruded polystyrene foam and expanded polystyrene in the external thermal insulation system: Recommended dosages: 1.0-2.0%. Tile adhesives (C1 and C2): Recommended dosage: 3.0-7.0% Storage and shelf life: Packaging: 25 kg paper bags. 18 bags per pallet. Big bags of 500 kg. The bags should be stored in a dry and cool warehouse at a temperature of 10 - 25 ° C. It is not advisable to stack the pallets one on top of the other to avoid caking due to the thermoplasticity of the polymer. The packaging should be closed after use to protect it from moisture and caking. The minimum shelf life is 12 months.
ORTHO CHLORO BENZALDEHYDE
Ortho Chloro benzaldehyde is a chlorinated derivative of benzaldehyde that is used in production of CS gas.
Ortho Chloro benzaldehyde reacts with malononitrile to form CS.
Ortho Chloro benzaldehyde is a clear colorless to yellowish liquid. (NTP, 1992)

CAS: 89-98-5
MF: C7H5ClO
MW: 140.57
EINECS: 201-956-3

Ortho Chloro benzaldehyde Chemical Properties
Melting point: 9-11 °C (lit.)
Boiling point: 209-215 °C (lit.)
Density: 1.248 g/mL at 25 °C (lit.)
Vapor density: 4.84 (vs air)
Vapor pressure: 1.27 mm Hg ( 50 °C)
Refractive index: n20/D 1.566(lit.)
Fp: 190 °F
Storage temp.: Store in RT
Solubility: 1.8g/l
Form: Liquid
Color: Clear colorless to light yellow
PH: 2.9 (H2O)(saturated aqueous solution)
Water Solubility: 0.1-0.5 g/100 mL at 24 ºC
Sensitive: Air Sensitive
BRN: 385877
Stability: Stable. Combustible.
Incompatible with strong oxidizing agents, strong bases, iron, strong reducing agents.
Moisture and light-sensitive.
LogP: 2.44 at 25℃
CAS DataBase Reference: 89-98-5(CAS DataBase Reference)
NIST Chemistry Reference: Ortho Chloro benzaldehyde (89-98-5)
EPA Substance Registry System: Ortho Chloro benzaldehyde (89-98-5)

Ortho Chloro benzaldehyde is a colorless to yellowish liquid with a penetrating odor.
Insoluble in water, soluble in benzene, alcohol and ether.
Ortho Chloro benzaldehyde is considerably more resistant to oxidation than benzaldehyde.
When Ortho Chloro benzaldehyde is heated with sodium sulfite solution under pressure, benzaldehyde-2-sulfonic acid forms.

Uses
Ortho Chloro benzaldehyde has been used in generation of small focused library of diversely functionalized dihydropyrimidine derivatives via one-pot three-component Biginelli cyclocondensation of β-ketoesters, aldehydes and thioureas.
Ortho Chloro benzaldehyde can be used to make alcohols, acids, and dyes; used in the rubber, tanning, and paper industries; used as an intermediate for optical brighteners, agricultural chemicals, and pharmaceuticals.
Ortho Chloro benzaldehyde can also be used to prepare triphenyl methane and related dyes, organic intermediate.
Ortho Chloro benzaldehyde is used acid zinc plating brightener, also be used for organic synthesis, agricultural pesticide and pharmaceutical industries.
Ortho Chloro benzaldehyde is used to synthesize the acaricides clofentezine and flutenzine.
Ortho Chloro benzaldehyde undergoes alkynylation with phenylacetylene in the presence of catalytic ligands and dimethylzinc at 0°C to form binaphthyl-derived amino alcohols.

Ortho Chloro benzaldehyde is used in manufacturing of electroplating, Dyes and API intermediates.
Ortho Chloro benzaldehyde can be used as zinc plating brightener.
Ortho Chloro benzaldehyde can also be used for organic synthesis, agricultural pesticide and pharmaceutical industries.
Ortho Chloro benzaldehyde is a kind of organic synthetic raw material; it can be applied in making of pharmacy and pesticide etc.
Ortho Chloro benzaldehyde can be used to make Chlorobenzylpenicillin sodium etc., as well as high efficient medical acaricide etc.

Ortho Chloro benzaldehyde is an intermediate of the plant growth regulator indyl ester.
Ortho Chloro benzaldehyde is used as intermediate of medicine and dye.
The dead Net of pesticide mites produced by Ortho Chloro benzaldehyde can control the mites on dry crops and fruit trees.
Ortho Chloro benzaldehyde can be obtained by O-chlorobenzoxime oximation, and O-chlorobenzoxime can be obtained by further chlorination, which are all drug intermediates.

Ortho Chloro benzaldehyde used as dye, pesticide, pharmaceutical intermediate.
Ortho Chloro benzaldehyde used as dye intermediate, also used in organic synthesis.
Ortho Chloro benzaldehyde, also known as 2-chlorobenzaldehyde, is the raw material for the synthesis of acaricide tetrarazine, it can also be used for the synthesis of another new acaricide, new species of fluxazine, and can also be used as a pharmaceutical, dye intermediate.
Ortho Chloro benzaldehyde important pharmaceutical, fuel and pesticide intermediates.
Ortho Chloro benzaldehyde is mainly used in medicine for synthesis of ampicillin (Cloxacillin).
Zinc plating brightener, mainly used in the manufacture of Ortho Chloro benzaldehyde, O-chlorobenzenes chloride and chlorbenzoxazole penicillin sodium and other pharmaceutical raw materials, is also widely used in the manufacture of pesticides on the high-efficiency acaricide, raw materials for dead-clean products of mites.
Preparation of triphenylmethane.

Preparation
Ortho Chloro benzaldehyde is produced mainly by chlorination of 2-chlorotoluene to form 2-chlorobenzal chloride, which is then subjected to acid hydrolysis.
Metal salts, such as iron(III) chloride, are used as catalysts.
The hydrolysis can also be accomplished using formic acid without a catalyst.
Ortho Chloro benzaldehyde can also be produced by oxidation of 2-chlorobenzyl chloride with N-oxides of tertiary amines or with dilute nitric acid.

Production Methods
Ortho Chloro benzaldehyde has the following 3 synthetic methods.

(1) Ortho Chloro benzaldehyde chlorination, hydrolysis method from O-chlorotoluene by chlorination, hydrolysis and.
(1) chlorination O-chlorotoluene, phosphorus trichloride and thionyl chloride are heated to 150 ° C., and chlorine gas is passed to a theoretical amount under ultraviolet irradiation to obtain O-chlorobenzylidene dichloride.

(2) ice solution the mixture of O-chlorobenzylidene dichloride and zinc chloride is heated at 120~130 ℃, and 1% ferric chloride aqueous solution is added dropwise with stirring, then heated and refluxed with water, the separated oil layer is refined O-chlorobenzaldehyde.
In addition, the hydrolysis may also be performed in the presence of sulfuric acid.
Stir O-chlorobenzylidene dichloride and industrial concentrated sulfuric acid together, and slowly heat for 12h to keep the temperature at 30~40 ℃ until the temperature is automatically lowered and the evolution of hydrogen chloride is slowed down, after stratification with cold water, the oily matter is separated, washed and distilled by steam to obtain the finished product.

(2) O-chlorotoluene chlorination, oxidation of O-chlorotoluene in the methyl chloride after nitric acid oxidation.
To a 3.0 ML Photo-reactor equipped with a thermometer, a stirrer, a chlorine gas blowing tube, a reflux condenser and a high-pressure mercury lamp illumination device, 380g (130 mol) of O-chlorotoluene was added and heated to ° C, under the light, the chlorine gas was blown into 1.5G/h (3.6 mol/h), and the time was h.
A total of 5.4mol chlorine gas was introduced.
After completion of the reaction, dry nitrogen was introduced into the reaction solution to drive out hydrogen chloride and chlorine gas to obtain a total of 558g of reaction solution, Among them, O-chlorotoluene 0.5%(mol), O-chlorobenzyl chloride 28%, O-chloro dichlorotoluene 67%, O-chloro trichlorotoluene 3%, O-chloro-chlorotoluene the average degree of chlorination is 1.8.
To a 2 L three-necked flask with thermometer, stirrer and reflux condenser, add 64.7g(0.343mol), 3%(mass fraction) of the above chlorinated mixture of O-chlorotoluene.
1440g of nitric acid and 2.0g of vanadium pentoxide were heated under reflux for 6h with stirring.
After completion of the reaction, the reaction mixture was cooled, 200ml of toluene was added, the oil phase was separated, and the aqueous layer was extracted twice by adding 100ml of toluene.
The oil phase and the extract were combined, toluene was distilled off, and the residue was distilled to obtain 36g of O-chlorobenzaldehyde from the 107~110 ℃(4.0kPa) fraction, with a yield of 73.5% based on O-chlorotoluene.

(3) O-chloro-dichlorotoluene was prepared by Catalytic Hydrolysis of O-chloro-dichlorotoluene.
Preparation example 1 0.034g of zinc oxide (1mol of raw material, 0.00084mol) was added to 97.7g of O-chlorotoluene, heated to 110 °c with stirring, and then 9.45ml of water was added slowly, the reaction was carried out at 110-120 ℃ for 1.9h.
After analysis and confirmation that the raw material O-chloro-dichlorotoluene completely disappeared, vacuum distillation was carried out under a nitrogen stream to collect a fraction at 97.1-98.3 ° C. (2.8kPa) to obtain 68.6g of O-chlorobenzaldehyde, with a yield of 97.6% and a content of 99.8%.
Preparation example 2 O-chloro dichlorotoluene 0.3g/min and water vapor 3g/min were added dropwise to the reactor, and 110 of water was added to the reactor in advance, and the water temperature was °c.

The resulting mixture of O-chloro-dichlorotoluene and water vapor was passed through a reaction tube layer of 50g of 5-10 mesh trialumina which had been heated to 118 ° C., and the resulting gas was cooled to obtain a suspension, which was extracted with diethyl ether and dried, the ether was distilled off and distilled under reduced pressure under a nitrogen stream to collect fractions at 96-98 ° C.
(2.93kPa) to obtain 68.8g of O-chlorobenzaldehyde, with a yield of 95.7% and a content of 97.8%.
The Ortho Chloro benzaldehyde side chain by chlorine and phosphorus trichloride chlorination process, Catalytic Hydrolysis, distillation refined.
The preparation method is to use benzaldehyde as a raw material, add a small amount of aluminum trichloride in the solvent dichloroethane as a catalyst for chlorination, and the reaction temperature is 25-30 ° C.
To obtain the product.
Ortho Chloro benzaldehyde can also be prepared by chlorination and hydrolysis of M-chlorotoluene.

Reactivity Profile
Ortho Chloro benzaldehyde reacts with iron and strong oxidizers, strong bases and strong reducing agents.

Health Hazard
Symptoms of exposure to Ortho Chloro benzaldehyde may include skin, eye and upper respiratory tract irritation.
Ortho Chloro benzaldehyde may cause skin, eye and respiratory tract irritation.
When heated to decomposition it emits toxic fumes.
Ortho Chloro benzaldehyde is combustible.

Synonyms
2-Chlorobenzaldehyde
89-98-5
O-CHLOROBENZALDEHYDE
Chlorobenzaldehyde
Benzaldehyde, 2-chloro-
Benzaldehyde, o-chloro-
2-Chlorbenzaldehyd
2-Clorobenzaldeide
o-Chloorbenzaldehyde
2-chloro-benzaldehyde
USAF M-7
2-Chloorbenzaldehyde
o-Chlorobenzenecarboxaldehyde
2-chloro benzaldehyde
BENZALDEHYDE,CHLORO-
NSC 15347
35913-09-8
MFCD00003304
QHR24X1LXK
DTXSID5024764
NSC-15347
2-Chlorbenzaldehyd [German]
o-Chloorbenzaldehyde [Dutch]
2-Chloorbenzaldehyde [Dutch]
2-Clorobenzaldeide [Italian]
CCRIS 5991
Benzaldehyde, chloro-
HSDB 2727
EINECS 201-956-3
UNII-QHR24X1LXK
chlorotoluon
AI3-04254
o-chlorobezaldehyde
2-chlorobezaldehyde
6-chlorobenzaldehyde
o-Chloroformylbenzene
o-chloro benzaldehyde
orthochlorobenzaldehyde
2- chlorobenzaldehyde
2-chlorobenzenaldehyde
NSC 174140
(2-chloro)benzaldehye
ortho-chlorobenzaldehyde
(2-chloro)benzaldehyde
(2-chloro) benzaldehyde
WLN: VHR BG
EC 201-956-3
2-Chlorobenzaldehyde, 99%
SCHEMBL97422
MLS001056242
CHLOROBENZALDEHYDE, O-
DTXCID204764
CHEMBL1547989
AMY39073
NSC15347
STR00143
Tox21_200373
STL146016
AKOS000119188
CS-W003973
CAS-89-98-5
NCGC00091218-01
NCGC00091218-02
NCGC00257927-01
SMR001216556
DS-006490
FT-0611908
FT-0611909
FT-0658390
EN300-19123
D77644
Q2195231
W-100351
2-Chlorobenzaldehyde, purum, dist., >=98.0% (GC)
F2190-0599
Z104472866
ORTHO CHLORO BENZALDEHYDE
o-Chlorobenzenecarboxyaldehyde; OCAD; 2-Chlorobenzene Carbonal; o-Chloorbenzaldehyde; 2-Chloorbenzaldehyde; 2-chlorbenzaldehyd; o-Chlorobenzaldehyde; 2-clorobenzaldeide; 2-Clorobenzaldehído; 2-Chlorobenzaldéhyde CAS:89-98-5
ORTHO PHENYL PHENOL
Ortho Phenyl Phenol is a broad spectrum fungicide used to protect crops in storage.
Ortho Phenyl Phenol is highly soluble in water, moderately voatile but is not expected to be persistent in the environment.
Ortho Phenyl Phenol is more selective than other free phenols but does produce phytotoxic effects.

CAS: 90-43-7
MF: C12H10O
MW: 170.21
EINECS: 201-993-5

Ortho Phenyl Phenol is a member of the class of hydroxybiphenyls that is biphenyl substituted by a hydroxy group at position 2.
Ortho Phenyl Phenol is generally used as a post-harvest fungicide for citrus fruits.
Ortho Phenyl Phenol has a role as an environmental food contaminant and an antifungal agrochemical.
Ortho Phenyl Phenol derives from a hydride of a biphenyl.
Ortho Phenyl Phenol, or o-phenylphenol, is an organic compound.
In terms of structure, Ortho Phenyl Phenol is one of the monohydroxylated isomers of biphenyl.
Ortho Phenyl Phenol is a white solid.
Ortho Phenyl Phenol is a biocide used as a preservative with E number E231 and under the trade names Dowicide, Torsite, Fungal, Preventol, Nipacide and many others.
Ortho Phenyl Phenol is a broad spectrum fungicide used to protect crops in storage.
Ortho Phenyl Phenol is highly soluble in water, moderately voatile but is not expected to be persistent in the environment.

Ortho Phenyl Phenol has a moderate to low toxicity to biodiversity.
Ortho Phenyl Phenol has a low oral mammalian toxicity, is carcinogenic, a neurotoxin and recognised irritant.
Ortho Phenyl Phenol, or o-phenylphenol, is an organic compound that consists of two linked benzene rings and a phenolic hydroxyl group.
Ortho Phenyl Phenol is a white or buff-colored, flaky crystalline solid with a melting point of about 57 °C.
Ortho Phenyl Phenol is a biocide used as a preservative under the trade names Dowicide, Torsite, Preventol, Nipacide and many others.
Ortho Phenyl Phenol or 2-Phenyl Phenol is a widely used chemical in the industrial sector that is known for its antimicrobial properties.

Ortho Phenyl Phenol is a phenolic compound produced through the condensation of phenol and formaldehyde and is commonly used as a preservative in a variety of applications, including wood preservation, cosmetics and personal care products, textiles, paints and coatings, adhesives, and agricultural products.
Ortho Phenyl Phenol is effective at preventing the growth of bacteria, fungi, and other microorganisms, making it a popular choice for companies looking to ensure the safety and quality of their products.
Ortho Phenyl Phenol is a very widely used organic chemical products, widely used in sterilization, printing and Dyeing auxiliaries and surfactants, synthetic new plastics, resin and polymer materials, stabilizers and flame retardants and other fields.
Ortho Phenyl Phenol and its sodium salt has a broad spectrum of sterilization in addition to mildew, and low toxicity and tasteless, is a good preservative, can be used for fruit and vegetable mold preservation, especially for citrus mold, can also be used for the treatment of lemon, pineapple, pear, peach, tomato, cucumber, etc., can reduce the decay to a minimum.

Ortho Phenyl Phenol Chemical Properties
Melting point: 57-59 °C(lit.)
Boiling point: 282 °C(lit.)
Density: 1.21
Vapor pressure: 7 mm Hg ( 140 °C)
Refractive index: 1.6188 (estimate)
FEMA: 3959 | 2-PHENYLPHENOL
Fp: 255 °F
Storage temp.: Store below +30°C.
Solubility: Soluble in ethanol, acetone, benzene,sodium hydroxide, chloroform, acetonitrile, toluene, hexane, ligroin, ethyl ether, pyridine, ethylene glycol, isopropanol, glycol ethers and polyglycols.
Form: Crystalline Flakes
pka: 10.01(at 25℃)
Color: White
Odor: nearly wh. or lt. buff crystals, mild char. sweetish odor
PH: 7 (0.1g/l, H2O, 20℃)
Explosive limit: 1.4-9.5%(V)
Water Solubility: 0.7 g/L (20 ºC)
Sensitive: Hygroscopic
Merck: 14,7304
JECFA Number: 735
BRN: 606907
Stability: Stable. Combustible.
Incompatible with strong oxidizing agents, halogens.
InChIKey: LLEMOWNGBBNAJR-UHFFFAOYSA-N
LogP: 3.18 at 22.5℃
CAS DataBase Reference: 90-43-7(CAS DataBase Reference)
NIST Chemistry Reference: o-Hydroxybiphenyl(90-43-7)
IARC: 3 (Vol. 73) 1999
EPA Substance Registry System: Ortho Phenyl Phenol (90-43-7)

Ortho Phenyl Phenol is a white to buff-colored crystalline solid with a distinct odor.
When heated to decomposition, Ortho Phenyl Phenol emits acrid smoke and irritating fumes.

Uses
Ortho Phenyl Phenol is a agriculture fungicide and is no longer used as a food additive.
Ortho Phenyl Phenol is remarkably versatile organic chemical products, widely used antiseptic, auxiliaries and surfactant synthesis of new plastics, resins and polymer materials in areas such as stabilizers and flame retardants.
Ortho Phenyl Phenol is used for the post-harvest control of storage diseases of apples, citrus fruit, stone fruit, tomatoes, cucumbers and other vegetables.
Ortho Phenyl Phenol is also used for the protection of textiles and timber and as a fungistat in water-soluble paints.

The primary use of Ortho Phenyl Phenol is as an agricultural fungicide.
Ortho Phenyl Phenol is generally applied post-harvest.
Ortho Phenyl Phenol is a fungicide used for waxing citrus fruits.
Ortho Phenyl Phenol is no longer a permitted food additive in the European Union, but is still allowed as a post-harvest treatment in 4 EU countries.

Ortho Phenyl Phenol is also used for disinfection of seed boxes.
Ortho Phenyl Phenol is a general surface disinfectant, used in households, hospitals, nursing homes, farms, laundries, barber shops, and food processing plants.
Ortho Phenyl Phenol can be used on fibers and other materials.
Ortho Phenyl Phenol is used to disinfect hospital and veterinary equipment.
Other uses are in rubber industry and as a laboratory reagent.
Ortho Phenyl Phenol is also used in the manufacture of other fungicides, dye stuffs, resins and rubber chemicals.

Ortho Phenyl Phenol is found in low concentrations in some household products such as spray disinfectants and aerosol or spray underarm deodorants.
The sodium salt of Ortho Phenyl Phenol, sodium orthophenyl phenol, is a preservative, used to treat the surface of citrus fruits.
Ortho Phenyl Phenol is also used as a fungicide in food packaging and may migrate into the contents.
The primary use of 2-phenylphenol is as an agricultural fungicide.
Ortho Phenyl Phenol is generally applied post-harvest.
Ortho Phenyl Phenol is a fungicide used for waxing citrus fruits.
As a food additive, Ortho Phenyl Phenol has E number E231.

Ortho Phenyl Phenol is also used for disinfection of seed boxes.
Ortho Phenyl Phenol is a general surface disinfectant, used in households, hospitals, nursing homes, farms, laundries, barber shops, and food processing plants.
Ortho Phenyl Phenol can be used on fibers and other materials.
Ortho Phenyl Phenol is used to sterilize hospital and veterinary equipment.
Other uses are in rubber industry and as a laboratory reagent.
Ortho Phenyl Phenol is also used in the manufacture of other fungicides, dye stuffs, resins and rubber chemicals.

Ortho Phenyl Phenol is found in low concentrations in some household products such as spray disinfectants and aerosol or spray underarm deodorants.
Eye contact can cause severe irritation and burns with possible eye damage.
For some individuals, Ortho Phenyl Phenol can also irritate the skin.
The sodium salt of Ortho Phenyl Phenol, sodium orthophenyl phenol, is a preservative, used to treat the surface of citrus fruits to prolong shelf life.
As a food additive, it has the E number E232.

Wood preservation: Ortho Phenyl Phenol is commonly used to protect wooden structures such as bridges, poles, and buildings from decay caused by fungi and insects.
Cosmetics and personal care products: Ortho Phenyl Phenol is used as a preservative in creams, lotions, shampoos, and other similar products to help keep them fresh and free of harmful microorganisms.
Textiles: Ortho Phenyl Phenol is used in the textile industry to prevent the growth of bacteria and fungi on fabric.
Paints and coatings: Ortho Phenyl Phenol is added to paint and coatings to prevent the growth of fungi and bacteria on surfaces.

Adhesives: Ortho Phenyl Phenol is used as a preservative in adhesives to prevent the growth of microorganisms and to maintain their effectiveness over time.
Agricultural products: Ortho Phenyl Phenol is used in agricultural products such as pesticides and herbicides to prevent the growth of fungi and bacteria.
Food preservation: Ortho Phenyl Phenol is used as a preservative in some food products, such as fruit juices and syrups, to prevent the growth of microorganisms.
However, please note that the use of Ortho Phenyl phenol in food products may be regulated by local laws and regulations, and it should only be used as directed.
Pharmaceuticals: OPP can be used as a preservative in topical medications or creams as well.

Ortho Phenyl Phenol is used as a carrier, surfactant, antiseptic and dye intermediate for hydrophobic synthetic fibers such as chlorinated polyamide and polyester.
In Japan, 2-hydroxybiphenyl and its sodium salt are used for the fungicide of citrus.
In the wax mixed with 0.8% of the goods, the use of spray method in the citrus after harvest, can also be used with biphenyl, rot blue to a minimum.
The range of fruits allowed to be used in the United Kingdom, the United States and Canada.

Ortho Phenyl Phenol use of O-Phenylphenol at high concentrations is suitable for inhibiting fungal growth (Fungistatic effect) or even for killing fungi (fungicidal effect).
CN200580026288 discloses the use of Ortho Phenyl Phenol and/or its derivatives for inhibiting asexual propagation of fungi, and also relates to filter media, adhesives, building materials, building accessories, fabrics, fur, paper, leather or leather products, as well as detergents, detergents, rinses, hand washes, hand dishwashing agents, automatic dishwashing agents, and for finishing building materials, building accessories, fabrics, fur, paper, reagents for leather or leather products, etc.

Preparation
Ortho Phenyl Phenol is prepared by condensation of cyclohexanone to give cyclohexenylcyclohexanone.
The latter undergoes dehydrogenation to give Ortho Phenyl Phenol.
Ortho Phenyl Phenol can be recovered from the distillation residue of the process of phenol production via sulfonation.
Ortho Phenyl Phenol distillation residue contains about 40% of phenyl phenol with the other components including phenol, inorganic salts, water and so on.
After vacuum distillation, the mixed phenyl phenol fraction is separated out with the vacuum being 53.3-66.7kPa.
The temperature, started to be cut at 65-75 ℃ to until 100 ℃ above, but should not higher than 1345 ℃.
Then take advantage of the solubility difference of ortho, p-hydroxy biphenyl in the trichlorethylene, the two are separated into pure product.
The mixed material (mainly 2-hydroxy biphenyl and 4-hydroxy biphenyl) is heated to be dissolved in the trichlorethylene, after cooling, first precipitate out 4-hydroxy biphenyl crystal.

After centrifuge filtration, dry to obtain 4-hydroxy biphenyl.
The mother liquor was washed with a sodium carbonate solution, followed by dilute alkaline to make the 2-hydroxybiphenyl salt.
After standing stratification, take the upper 2-hydroxybiphenyl sodium salt for dehydration under reduced pressure, namely, sodium salt products.
The 2-hydroxybiphenylsodium salt is white to light red powder, being easily soluble in water with the solubility in 100g of water being 122g.
The pH value of the 2% aqueous solution is 11.1-12.2.
Ortho Phenyl Phenol is also easily soluble in acetone, methanol, soluble in glycerol, but insoluble in oil.
The sodium salt of 2-hydroxy biphenyl, after acidification, can lead to the formation of 2-hydroxy biphenyl with both of them being food additives.

Reactivity Profile
Ortho Phenyl Phenol react as a weak organic acid.
Exothermically neutralizes bases.
May react with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides to generate flammable gas (H2) and the heat of the reaction may ignite the gas.
Is sulfonated very readily (for example, by concentrated sulfuric acid at room temperature) in exothermic reactions.
May be nitrated very rapidly.
Nitrated phenols often explode when heated and also form metal salts that tend toward detonation by rather mild shock.
Can react with oxidizing agents.

Carcinogenicity
IARC classified SOPP as a B2 carcinogen in 1983, based on reports from Japan that high dietary levels of this sodium salt caused bladder tumors in male rats.
Both sodium saccharin and sodium cyclamate also cause bladder tumors at high doses in male rats, but classification of these food additives as B2 carcinogens was recently rescinded by IARC at a meeting in 1998.
The U.S. National Toxicology Program conducted a skin painting study with OPP in groups of 50 mice per sex.
The Ortho Phenyl Phenol was applied as an acetone solution on 3 days per week for 2 years, both alone and as a promoter with DMBA.
No skin neoplasms were observed in either sex treated with OPP alone, and there were no tumor enhancing or inhibiting effects when Ortho Phenyl Phenol and DMBA were given in combination.

Metabolic pathway
Ortho Phenyl Phenol is not used on growing plants because it is too phytotoxic and there appears to be no information published on its metabolism in plants.
Ortho Phenyl Phenol's widespread use as a preservative, disinfectant and fungistat on stored food (either by direct application or impregnated in packaging) requires studies on its environmental fate and metabolism in mammals.
Several studies in mammals are available and the compound has been the subject of an evaluation by the UK MAFF Pesticide Safety Directorate (PSD); the results have been published (PSD, 1993).

This evaluation was prompted by the discovery of bladder tumours in rats treated with high doses of the compound.
Ortho Phenyl Phenol is also used as the sodium and potassium salts where water solublity is important.
No information is available specifically on the latter.
The metabolism of the free phenol and the sodium salt have been studied separately.
Once absorbed into a cell, provided that internal pH control is maintained, the two forms should be indistinguishable.

Toxicity evaluation
Ortho Phenyl Phenol has a moderate to low toxicity to biodiversity.
Ortho Phenyl Phenol has a low oral mammalian toxicity, is carcinogenic, a neurotoxin and recognised irritant.
Ortho Phenyl Phenol and its sodium salt have a low acute toxicity in mammals when administered orally, with LD50 values ranging from 600 to 3500 mg/kg of body weight.

Synonyms
2-Phenylphenol
2-Hydroxybiphenyl
90-43-7
O-PHENYLPHENOL
Biphenyl-2-ol
2-Biphenylol
o-Hydroxybiphenyl
2-Hydroxydiphenyl
o-Hydroxydiphenyl
o-Phenyl phenol
Phenylphenol
Biphenylol
Orthophenylphenol
Orthoxenol
o-Diphenylol
[1,1'-Biphenyl]-2-ol
Dowicide 1
Torsite
o-Xenol
o-Biphenylol
Preventol O extra
Orthohydroxydiphenyl
Nectryl
(1,1'-Biphenyl)-2-ol
Tumescal OPE
ortho-Phenylphenol
Remol TRF
Phenol, o-phenyl-
Tetrosin oe
1-Hydroxy-2-phenylbenzene
2-Fenylfenol
2-Hydroxybifenyl
o-Xonal
2-Phenyl phenol
Biphenyl, 2-hydroxy-
Invalon OP
Anthrapole 73
2-hydroxy biphenyl
Usaf ek-2219
1,1'-Biphenyl-2-ol
Dowicide
Kiwi lustr 277
Hydroxdiphenyl
(1,1-Biphenyl)-2-ol
o-phenylphenate
o-Phenylphenol, cosmetic grade
Phenyl-2 phenol
Dowicide 1 antimicrobial
Orthophenyl phenol
ortho-phenylphenate
orthohydroxydipbenyl
Biphenyl-2-o1
NCI-C50351
Hydroxybiphenyl
2-Fenylfenol [Czech]
Hydroxy-2-phenylbenzene
Caswell No. 623AA
C12H10O
2-Hydroxybifenyl [Czech]
Nipacide OPP
NSC 1548
2-Hydroxy-1,1'-biphenyl
OPP [pesticide]
Tumescal 0PE
2-Phenylphenol [BSI:ISO]
2-Phenylphenol-d5
CCRIS 1388
Phenyl-2 phenol [ISO-French]
HSDB 1753
EINECS 201-993-5
EPA Pesticide Chemical Code 064103
BRN 0606907
UNII-D343Z75HT8
AI3-00062
CHEMBL108829
DTXSID2021151
CHEBI:17043
D343Z75HT8
NSC-1548
E231
EC 201-993-5
4-06-00-04579 (Beilstein Handbook Reference)
DTXCID201151
Lyorthol
CAS-90-43-7
sodium o-phenylphenoate
sodium ortho-phenylphenol
Stellisept
Rotoline
Xenol
o-phenyl-phenol
2-phenyl-phenol
Tetrosin OE-N
Phenylphenol, 2-
Biphenyl- 2- ol
Amocid (TN)
MFCD00002208
Preventol 3041
ORTOFENILFENOL
Phenol, 2-phenyl-
2-Phenylphenol [C]
Phenylphenol (ortho-)
2-Phenylphenol, 99%
OPP?
PHENYLPHENOL, O-
Hydroxy-2-ph enylbenzene
WLN: QR BR
ORTHO PHENYL PHENOL
[1,1'-bifenil]-2-ol
O-PHENYLPHENOL [MI]
2-Phenylphenol, BSI, ISO
SCHEMBL29811
MLS002415765
2-PHENYLPHENOL [ISO]
BIDD:ER0664
O-PHENYLPHENOL [INCI]
[1,1''-biphenyl]-2-ol
2-PHENYLPHENOL [FHFI]
2-PHENYLPHENOL [HSDB]
FEMA 3959
2-Phenylphenol, >=99%, FG
NSC1548
ORTHO-PHENYLPHENOL [IARC]
ORTHOPHENYLPHENOL [MART.]
ORTHOPHENYLPHENOL [WHO-DD]
AMY40390
STR07240
EINECS 262-974-5
Tox21_202415
Tox21_300674
BDBM50308551
ORTHOPHENYL PHENOL (E 231)
STK177354
AKOS000118750
LS-1912
PS-8698
NCGC00091595-01
NCGC00091595-02
NCGC00091595-03
NCGC00091595-04
NCGC00091595-05
NCGC00091595-06
NCGC00254582-01
NCGC00259964-01
2-Phenylphenol 100 microg/mL in Acetone
AC-10362
SMR000778031
2-Phenylphenol 10 microg/mL in Cyclohexane
2-Phenylphenol 1000 microg/mL in Acetone
2-Phenylphenol 10 microg/mL in Acetonitrile
BB 0223993
FT-0654846
P0200
1,1'-BIPHENYL-2-OL; 2-PHENYLPHENOL
EN300-19380
C02499
D08367
E79453
2-Phenylphenol, PESTANAL(R), analytical standard
Q209467
SR-01000944520
SR-01000944520-1
W-100332
F0001-2206
Z104473674
61788-42-9
CH9
ORTHO PHTHALALDEHYDE
Ortho Phthalaldehyde Phthalaldehyde (sometimes also o-phthalaldehyde or ortho-phthalaldehyde, Ortho phthalaldehyde) is the chemical compound with the formula C6H4(CHO)2. It is one of three isomers of benzene dicarbaldehyde, related to phthalic acid. This pale yellow solid is a building block in the synthesis of heterocyclic compounds and a reagent in the analysis of amino acids. Ortho phthalaldehyde dissolves in water solution at pH < 11.5. Its solutions degrade upon UV illumination and exposure to air. Ortho phthalaldehyde: a possible alternative to glutaraldehyde for high level disinfection Ortho phthalaldehyde (OPA) was tested against a range of organisms including glutaraldehyde-resistant mycobacteria, Bacillus subtilis spores and coat-defective spores. Glutaraldehyde (GTA) and peracetic acid (PAA) were tested for comparative purposes. Both suspension and carrier tests were performed using a range of concentrations and exposure times. All three biocides were very effective (> or = 5 log reduction) against Escherichia coli, Staphylococcus aureus and Pseudomonas aeruginosa in suspension tests. Ortho phthalaldehyde and GTA (PAA was not tested) were also very effective against Staph. aureus and Ps. aeruginosa in carrier tests. Ortho phthalaldehyde showed good activity against the mycobacteria tested including the two GTA-resistant strains, but 0.5% w/v Ortho phthalaldehyde was found not to be sporicidal. However, limited activity was found with higher concentrations and pH values. Coat-defective spores were more susceptible to Ortho phthalaldehyde, suggesting that the coat may be responsible for this resistance. The findings of this study suggest that Ortho phthalaldehyde is effective against GTA-resistant mycobacteria and that it is a viable alternative to GTA for high level disinfection. USES of Ortho Phthalaldehyde A reagent that forms fluorescent conjugation products with primary amines. It is used for the detection of many biogenic amines, peptides, and proteins in nanogram quantities in body fluids. Synthesis and reactions The compound was first described in 1887 when it was prepared from α,α,α’,α’-tetrachloro-ortho-xylene.[4] A more modern synthesis is similar: the hydrolysis of the related tetrabromo-o-xylene using potassium oxalate, followed by purification by steam distillation.[2] The reactivity of Ortho phthalaldehyde is complicated by the fact that in water it forms both a mono- and dihydrate, C6H4(CHO)(CH(OH)2) and C6H4(CH(OH))2O, respectively. Its reactions with nucleophiles often involves the reaction of both carbonyl groups.[5] Orthophthalaldehyde and hydrated forms 001.png Biochemistry Ortho phthalaldehyde is used in a very sensitive fluorescent reagent for assaying amines or sulfhydryls in solution, notably contained in proteins, peptides, and amino acids, by capillary electrophoresis and chromatography. Ortho phthalaldehyde reacts specifically with primary amines above their isoelectric point Pi in presence of thiols. Ortho phthalaldehyde reacts also with thiols in presence of an amine such as n-propylamine or 2-aminoethanol. The method is spectrometric (fluorescent emission at 436-475 nm (max 455 nm) with excitation at 330-390 nm (max. 340 nm)).[6] Disinfection Ortho phthalaldehyde is commonly used as a high-level disinfectant for medical instruments, commonly sold under the brand names of Cidex Ortho phthalaldehyde or TD-8. Disinfection with Ortho phthalaldehyde is indicated for semi-critical instruments that come into contact with mucous membranes or broken skin, such as specula, laryngeal mirrors, and internal ultrasound probes. Poly(phthalaldehyde) Ortho phthalaldehyde can be polymerized. In the polymer, one of the oxygen atoms forms a bridge to the other non-ring carbon of the same phthalaldehyde unit, while the other bridges to a non-ring carbon of another phthalaldehyde unit. Poly(phthalaldehyde) is used in making a photoresist. In winemaking The Nitrogen by O-Phthaldialdehyde Assay (NOrtho phthalaldehyde) is one of the methods used in winemaking to measure yeast assimilable nitrogen (or YAN) needed by wine yeast in order to successfully complete fermentation.[9] Isomeric phthalaldehydes Related to phthalaldehyde are: isophthalaldehyde (benzene-1,3-dicarbaldehyde; m.p. 87–88 °C, CAS# 626-19-7) terephthalaldehyde (benzene-1,4-dicarbaldehyde; m.p. 114–116 °C, CAS# 623-27-8) Properties Chemical formula C8H6O2 Molar mass 134.134 g·mol−1 Appearance Yellow solid Density 1.19 g/mL Melting point 55.5 to 56 °C (131.9 to 132.8 °F; 328.6 to 329.1 K)[2] Boiling point 266.1 °C (511.0 °F; 539.2 K) Solubility in water Low Ortho Phthalaldehyde is a known environmental transformation product of Dithianon. Ortho phthalaldehyde is mainly used as a high-level disinfectant (a low-temperature chemical method) for heat-sensitive medical and dental equipment such as endoscopes and thermometers; in recent years, it has gained popularity as a safe and better alternative to glutaraldehyde. There are some researches show, pH7.5 contains the sterilizing agent of Ortho phthalaldehyde 0.5%, and its sterilizing power, sterilization speed, stability and toxicity all are better than glutaraldehyde, can kill mycobacterium in the 5min, the bacterium number reduces by 5 logarithmic value, and Ortho phthalaldehyde is very stable, tasteless in pH3~9 scopes, non-stimulated to human nose, eye mucosa, and need not activate before using, various materials are had good consistency, have tangible microbiocidal activity. USES of Ortho phthalaldehyde Ortho phthalaldehyde can be widely used for precolumn derivatization of amino acids in HPLC separation or Capillary electrophoresis. For flow cytometric measurements of protein thiol groups. Uses Ortho phthalaldehyde can be used for precolumn derivatization of amino acids for HPLC separation and for flow cytometric measurements of protein thiol groups. Uses Precolumn derivatization reagent for primary amines and amino acids. The fluorescent derivative can be detected by reverse-phase HPLC. The reaction requires OPA, primary amine and a sulfhydryl. In the presence of excess sulfhydryl, amines can be quantitated. In the presence of excess amine, sulfhydryls can be quantitated. Uses Disinfectant. Reagent in fluorometric determination of primary amines and thiols. Preparation Ortho phthalaldehyde is a high-level chemical disinfectant that is commonly used for disinfection of dental and medical instruments as an alternative to glutaraldehyde, which is a known skin and respiratory sensitizer. A variety of processes for manufacturing Ortho phthalaldehyde have been reported in the literature. Ortho phthalaldehyde is produced by heating pure benzaldehyde and chloroform with potassium hydroxide solution. The resulting solution is further acidified with hydrochloric acid and cooled to yield a colorless powder of Ortho phthalaldehyde. It is also produced by ozonization of naphthalene in alcohol followed by catalytic hydrogenation. Catalytic oxidation of various chemicals is also used in manufacturing Ortho phthalaldehyde. Ortho phthalaldehyde can be manufactured by oxidation of phthalan by nitrogen monoxide in acetonitrile with N-hydroxyphthalimide as the catalyst to yield 80% to 90%. Ortho phthalaldehyde is a pale, yellow crystal or colorless powder. It is soluble in water. USE: Ortho phthalaldehyde is used as a disinfectant, mainly for dental and medical equipment. EXPOSURE: Workers that produce or use Ortho phthalaldehyde may have direct skin contact. The general population may be exposed by contact with residual disinfectant. If Ortho phthalaldehyde is released to the environment, it will be broken down in air by reaction with hydroxyl radicals. It may be broken down in the air by sunlight. It will not volatilize into air from soil or water surfaces. It is expected to move easily through soil. It is not expected to build up in fish. RISK: Irritation to the skin, eyes, and respiratory tract as well as asthma and allergic skin rashes have been reported in some healthcare workers that routinely use Ortho phthalaldehyde to disinfect equipment. Severe anaphylactic allergic reactions have been reported in some patients exposed to equipment disinfected with Ortho phthalaldehyde. Discoloration of the mouth and throat, burning of the throat, nausea, vomiting, and diarrhea may occur with ingestion. Damage to the nose, throat, lung, skin, and eyes were observed in laboratory animals following repeated exposure to low air levels of Ortho phthalaldehyde, damage was severe at moderate air levels and some animals died. Several alterations in the blood were also observed. Damage to the gastrointestinal tract, irregular breathing, impaired movement, and changes in the blood were observed in laboratory animals given moderate oral doses. Some animals died at high oral doses. No evidence of abortion or birth defects were noted in laboratory animals exposed to Ortho phthalaldehyde during pregnancy, but delayed bone development was observed at high doses that made the mothers sick. Data on the potential for Ortho phthalaldehyde to cause infertility in laboratory animals were not available. However, damage to the testis and reduced sperm counts and motility were observed in male animals following repeated exposure to low air levels of Ortho phthalaldehyde. Data on the potential for Ortho phthalaldehyde to cause cancer in laboratory animals were not available. The potential for Ortho phthalaldehyde to cause cancer in humans has not been assessed by the U.S. EPA IRIS program, the International Agency for Research on Cancer, or the U.S. National Toxicology Program 14th Report on Carcinogens. For Ortho phthalaldehyde (USEPA/OPP Pesticide Code: 129017) there are 0 labels match. /SRP: Not registered for current use in the USA, but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses. Recently, the use of ortho phthalaldehyde (OPA) has been increasing as an alternative to glutaraldehyde(GA)for endoscope disinfection. We detected development of bronchial asthma and contact dermatitis in health care workers (HCW) employed in an endoscopy unit. ... Two of 83 health care workers described mild eye irritation, but no contact dermatitis or bronchitis had newly developed. Three sampling and analytical methods have been developed and evaluated for Ortho phthalaldehyde (OPA): (1) an HPLC-UV method for Ortho phthalaldehyde in air, (2) a fluorimetric method for Ortho phthalaldehyde on surfaces, and (3) a colorimetric method for Ortho phthalaldehyde on surfaces. (1) The air sampler contains 350 mg of silica gel coated with 1 mg of acidified 2,4-dinitrophenylhydrazine (DNPH). Air sampling may be conducted at 0.03 to 1.0 L/min for periods up to 8 hr. Samples were eluted with ethyl acetate, and the eluents were allowed to stand for 72 hr. Analysis was by high performance liquid chromatography (HPLC) with a UV detector set at 369 nm. An unusual phenomenon was the observation that the stability of the sample on a sampler at 3 degrees C tends to decrease as the total quantity of Ortho phthalaldehyde collected on the sampler decreases. Elution of the samples within 24 hr of air sampling is required. The detection limit (LOD) is approximately 0.02 ug of Ortho phthalaldehyde per sample. Ortho phthalaldehyde on surfaces may be collected with strips cut from a sheet of polyvinyl alcohol (PVA wipe). (2) In the surface wipe method with analysis by fluorescence measurement, the strips of PVA wipe were placed into dimethyl sulfoxide. An aliquot was treated with aqueous N-acetyl-l-cysteine and ethylenediamine. Analysis was performed with a portable fluorometer (excitation and emission wavelengths = 365 nm and 438 nm, respectively). The LOD is 0.2 ug per sample. (3) In the surface wipe method with visual colorimetric detection, the strips of PVA wipe were placed into 30:70 acetonitrile:water. An aliquot was treated with N-(1-naphthyl)ethylenediamine in 0.1 m sulfuric acid. After color development, the LOD is approximately 48 ug per sample. These methods have been field tested in a hospital. A simple high performance liquid chromatographic (HPLC) method and a highly sensitive gas chromatography mass spectrometric (GC-MS) method have been established for the determination of Ortho phthalaldehyde (OPA) in water. These methods are based on the derivatization of Ortho phthalaldehyde with hydrazine in water. The following optimum reaction conditions were established: reagent dosage, 20 mg/mL of hydrazine; pH 2; reaction for 20 min at 70 °C. The organic derivative was detected directly by HPLC or after the extraction with methylene chloride/concentration by GC-MS. The limit of detection of Ortho phthalaldehyde in water was 4.0 and 0.3 ug/L by HPLC and GC-MS, respectively. The calibration curve showed good linearity with r2 = 0.9993 and r2 = 0.9994 by HPLC and GC-MS, respectively, the accuracy was in a range of 95-105%, and the precision of the assay was less than 13% in water. The HPLC method was simple and reproducible enough to permit the Ortho phthalaldehyde content analysis in the disinfectant products, and the GC-MS method is sensitive enough to permit reliable analysis of Ortho phthalaldehyde to the ug/L level in environmental water. 2018 Notice of Intended Changes (NIC): These substances, with their corresponding values and notations, comprise those for which (1) a limit is proposed for the first time, (2) a change in the Adopted value is proposed, (3) retention as an NIC is proposed, or (4) withdrawal of the Documentation and adopted TLV is proposed. In each case, the proposals should be considered trial values during the period they are on the NIC. These proposals were ratified by the ACGIH Board of Directors and will remain on the NIC for approximately one year following this ratification. If the Committee neither finds nor receives any substantive data that changes its scientific opinion regarding an NIC TLV, the Committee may then approve its recommendation to the ACGIH Board of Directors for adoption. If the Committee finds or receives substantive data that change its scientific opinion regarding an NIC TLV, the Committee may change its recommendation to the ACGIH Board of Directors for the matter to be either retained on or withdrawn from the NIC. Substance: Ortho Phthalaldehyde; Time Weighted Avg (TWA): Surface Limit 0.025 mg/100 sq cm; Short Term Exposure Limit (STEL): Ceiling 0.0001 ppm (vapor fraction); Notations: Skin, Dermal Sensitization, Respiratory Sensitization; Molecular Weight: 134.10; TLV Basis: Eye, skin & respiratory tract irritation; respiratory sensitization; anaphylaxis. IDENTIFICATION AND USE: Ortho Phthalaldehyde (Ortho phthalaldehyde) is used as disinfectant and reagent in fluorometric determination of primary amines and thiols. HUMAN STUDIES: Ortho phthalaldehyde is a commonly used solution for rapid sterilization of medical equipment. Cases of anaphylaxis following cystoscopy with endoscopes sterilized with this agent have been reported. Ortho phthalaldehyde-induced anaphylaxis following laryngoscopy have also been described. In these patients, Ortho phthalaldehyde-specific IgE was detected in the serum. Contact dermatitis occurred in 4 workers of the endoscopy unit, one of whom also developed asthma. Among 80 female disinfection workers who used only antiseptic solutions containing Ortho phthalaldehyde, the incidence of disinfection-related complaints were 10% skin, 9% eye, and 16% respiratory symptoms. ANIMAL STUDIES: In male mice, injected Ortho phthalaldehyde induced specific IgE and IgG in the sera, suggesting that Ortho phthalaldehyde acts as a hapten. Overall, Ortho phthalaldehyde caused acute inflammation and acted as a haptenic allergen, although it caused only mild liver injury. In mice sensitized to ovalbumin (OVA), Ortho phthalaldehyde enhanced the OVA-induced recruitment of neutrophils to the lung and the production of allergen-specific IgE, suggesting that Ortho phthalaldehyde acts as an immunological adjuvant. The major targets from Ortho phthalaldehyde exposure in rats and mice included the respiratory system (nasal cavity, larynx, trachea, and lung), skin, eye, testis, and epididymis. The most sensitive measure of Ortho phthalaldehyde inhalation toxicity in male and female rats and mice was significantly increased incidences of nasal cavity lesions (lowest-observable-effect concentration = 0.44 ppm). Ortho phthalaldehyde was mutagenic in Salmonella typhimurium strain TA100 in the absence of exogenous metabolic activation; no mutagenicity was seen in TA100 with metabolic activation or in TA98 or Escherichia coli WP2 uvrA/pKM101, with or without metabolic activation. Iatrogenic injury from medical disinfectants is an uncommon but potentially devastating complication. We report an unusual, but severe, upper aerodigestive complication from the use of Ortho phthalaldehyde solution, a commonly used endoscope disinfectant. Ortho phthalaldehyde (Cidex Ortho phthalaldehyde) is a commonly used solution for rapid sterilization of flexible endoscopic equipment. We report two cases of anaphylaxis following cystoscopy with endoscopes sterilized with this agent. Only a handful of such reactions have been reported in the published literature, the majority of which are in the bladder cancer population undergoing surveillance cystoscopy. PATIENTS AND METHODS: We reviewed the clinical presentation of two cases of anaphylaxis following flexible cystoscopy with instruments sterilized with Ortho phthalaldehyde. We further describe their subsequent evaluation by an allergy and immunology specialist who performed skin testing to confirm a suspected Ortho phthalaldehyde allergy. RESULTS: Both patients were skin test positive to Ortho phthalaldehyde antigen. As a result, sterilization techniques for our flexible endoscopes has been altered. To date, no further anaphylactic reactions have occurred in our bladder cancer patients, including the two cases presented herein following subsequent cystoscopic evaluations. CONCLUSIONS: Ortho phthalaldehyde-sterilized cystoscopes have been associated with anaphylactic reactions in a small number of patients who have undergone repeated cystoscopy. The manufacturer has already made recommendations to avoid this agent in bladder cancer patients. It may be prudent to extend this practice to other populations undergoing repeat cystoscopy. Ortho phthalaldehyde (OPA) has recently been used as a disinfectant for various medical apparatuses. Ortho phthalaldehyde is not generally recognized as a potential allergen. CASE SUMMARY: Subsequent to our recent report describing a patient presenting with Ortho phthalaldehyde-induced anaphylaxis following laryngoscopy, we experienced two more such cases. In all three cases, the basophil histamine release test was useful for identifying the allergen as Ortho phthalaldehyde. Ortho phthalaldehyde-specific IgE was successfully detected in the serum of the patients by ELISA. DISCUSSION: Physicians and co-medical workers need to be aware of potential allergens to which patients may be exposed during routine medical procedures. Because body fluids and blood have a tendency to adhere to transesophageal echo devices, a high level of sterilization is required when cleaning them. Ortho phthalaldehyde (OPA) has been widely used in Japan since being approved as a high-level sterilant. The authors report a patient with widespread, severe skin and mucous membrane damage of the lip, tongue, pharynx and esophagus areas that was attributed to inadequate washing after the sterilization of a transesophageal echo device with Ortho phthalaldehyde. This patient experienced sequelae, which did not improve after more than 1 year of continuous treatment. When using medical devices sterilized with Ortho phthalaldehyde, the use of a probe cover, when applicable, is recommended and complete washing prior to use is required. Acute Exposure/ Although Ortho phthalaldehyde (OPA) has been suggested as an alternative to glutaraldehyde for the sterilization and disinfection of hospital equipment, the toxicity has not been thoroughly investigated. The purpose of these studies was to evaluate the irritancy and sensitization potential of Ortho phthalaldehyde. The EpiDerm Skin Irritation Test was used to evaluate in vitro irritancy potential of Ortho phthalaldehyde and glutaraldehyde. Treatment with 0.4125 and 0.55% Ortho phthalaldehyde induced irritation, while glutaraldehyde exposure at these concentrations did not. Consistent with the in vitro results, Ortho phthalaldehyde induced irritancy, evaluated by ear swelling, when mice were treated with 0.75%. Initial evaluation of the sensitization potential was conducted using the local lymph node assay at concentrations ranging from 0.005 to 0.75%. A concentration-dependent increase in lymphocyte proliferation was observed with a calculated EC3 value of 0.051% compared to that of 0.089%, previously determined for glutaraldehyde. Immunoglobulin (Ig) E-inducing potential was evaluated by phenotypic analysis of draining lymph node (DLN) cells and measurement of total and specific serum IgE levels. The 0.1 and 0.75% exposed groups yielded significant increases in the IgE+B220+ cell population in the lymph nodes while the 0.75% treated group demonstrated significant increases in total IgE, Ortho phthalaldehyde-specific IgE, and Ortho phthalaldehyde-specific IgG(1). In addition, significant increases in interleukin-4 messenger RNA and protein expression in the DLNs were observed in Ortho phthalaldehyde-treated groups. The results demonstrate the dermal irritancy and allergic potential of Ortho phthalaldehyde and raise concern about the proposed/intended use of Ortho phthalaldehyde as a safe alternative to glutaraldehyde. Acute Exposure/ Ortho phthalaldehyde (OPA) has been used as a safe alternative disinfectant instead of glutaraldehyde; however, recently some adverse effects of Ortho phthalaldehyde were reported in patients and medical professions. We examined the acute toxicity of Ortho phthalaldehyde in male ICR mice injected with 0.125-0.5% Ortho phthalaldehyde and killed some animals 1 day after a single Ortho phthalaldehyde injection, and others 1 or 13 days after two Ortho phthalaldehyde injections 5 days apart. Hematology, blood cell counts, specific antibody production, organ weights, hepatic enzymes, hepatic histOrtho phthalaldehydethology and gene expression of cytochrome P450 (CYP) mRNA in liver were examined. Single Ortho phthalaldehyde injections elevated leukocyte counts, the proportion of neutrophils, alanine aminotransferase (ALT) and aspartate aminotransferase (AST). Two Ortho phthalaldehyde injections dose-dependently increased leukocyte counts, the proportion of neutrophils, ALT and AST, and decreased alkaline phosphatase. Leukocyte counts and proportions of neutrophils normalized 13 days after the second of two injections. However, both ALT and AST remained high in mice given higher Ortho phthalaldehyde doses. Significant increased liver-to-body weight ratio and mild hepatic lesions were observed. Gene expression of CYP1a1 and CYP2e1 revealed a tendency of up-regulation 1 day after two Ortho phthalaldehyde injections. However, expression of these genes was then down-regulated 13 days after Ortho phthalaldehyde injections. Ortho phthalaldehyde induced specific IgE and IgG significantly in the sera, suggesting that Ortho phthalaldehyde acts as a hapten. Overall, Ortho phthalaldehyde caused acute inflammation and acted as a haptenic allergen, although it caused only mild liver injury. Such evidence suggested that careful washing and prevention of exposure were needed after Ortho phthalaldehyde disinfection of medical instruments. Developmental or Reproductive Toxicity/ The general population is exposed to phthalates through consumer products, diet, and medical devices. Phthalic acid (PA) is a common final metabolite of phthalates, and its isomers include isophthalic acid (IPA), terephthalic acid (TPA), and phthalaldehyde (o-phthalic acid, Ortho phthalaldehyde). The purpose of this study was to investigate whether PA and PA isomers exert reproductive toxicity, including altered sperm movement. In vitro cell viability assays were comparatively performed using Sertoli and liver cell lines. In animal experiments, PA or PA isomers (10, 100, or 1000 mg/kg) were administered orally to Sprague-Dawley (SD) rats, and semen samples were analyzed by computer-aided sperm analysis (CASA). PA treatment produced a significant effect on curvilinear velocity (VCL), straight-line velocity (VSL), mean velocity or average path velocity (VAP), amplitude of lateral head displacement (ALH), and frequency of head displacement or beat cross-frequency (BCF), whereas IPA, TPA, and Ortho phthalaldehyde induced no marked effects. In vitro cell viability assays showed that mouse normal testis cells (TM4) and human testis cancer cells (NTERA 2 cl. D1) were more sensitive to PA and Ortho phthalaldehyde than mouse liver normal cells (NCTC clone 1469) and human fetal liver cells (FL 62891). Our study suggests that PA and PA isomers specifically produced significant in vitro and in vivo reproductive toxicity, particularly sperm toxicity and testis cell cytotoxicity. Of the isomers examined, PA appeared to be the most toxic and may serve as a surrogate biomarker for reproductive toxicity following mixed exposure to phthalates. Neurotoxicity/ Glutaraldehyde (GA) and ortho-phtalaldehyde (Ortho phthalaldehyde) have been widely used as major components of disinfectants in hospitals. We evaluated the alterations in GA or Ortho phthalaldehyde in rats after subacute inhalation exposure by determining levels of neurotransmitters (norepinephrine [NE], dOrtho phthalaldehydemine [DA], DA metabolites, dihydroxyphenylacetic acid [DOrtho phthalaldehydeC] and homovanillic acid [HVA], indoleamine serotonin [5-HT] and 5-HT metabolite, 5-hydroxyindoleacetic acid [5-HIAA]) in discrete brain regions using high performance liquid chromatography (HPLC) equipped with an electrochemical detector. Female Wistar rats were exposed to 0, 50, 100, or 200 ppb gaseous GA or Ortho phthalaldehyde by inhalation for 1 hr per day, 5 d per week for 4 wk. Following the exposure, the brain of each rat was removed and dissected into cerebrum, cerebellum, medulla oblongata, midbrain, corpus striatum and hypothalamus. The neurotransmitters and their metabolites were extracted from each brain region, and determined by HPLC. Regarding GA, the daily water intake of the 50 or the 200 ppb exposed groups was significantly lower than that of the control. DA and 5-HIAA levels in the medulla oblongata among the GA exposed groups were significantly lower than those of the control. For Ortho phthalaldehyde, the mean final body weight and daily food intake of the 100 or 200 ppb exposed groups were significantly lower than those of the control. The mean DA concentrations in the cerebrum in the groups exposed to Ortho phthalaldehyde were significantly lower than those of the control. Ortho phthalaldehyde may modulate DA metabolism in the cerebrum of female rats. The levels GA or Ortho phthalaldehyde that induced alienations in neurotransmitters were comparable to those levels usually found in hospitals, further studies are warranted to evaluate the of safety of disinfectants containing GA or Ortho phthalaldehyde. Groups of 10 male and 10 female rats and mice were exposed to Ortho Phthalaldehyde at concentrations of 0, 0.44, 0.88, 1.75, 3.5, or 7.0 ppm, 6 hours plus T90 (17 minutes) per day, 5 days per week for 14 weeks; additional groups of 10 male and 10 female clinical pathology study rats were exposed to the same concentrations for 23 days. All rats exposed to 7.0 ppm died by the end of week 2 of the study, and seven males and two females exposed to 3.5 ppm died by week 7 of the study. All mice exposed to 7.0 ppm died during week 1 of the study, and five males and four females exposed to 3.5 ppm died by week 6 of the study. Clinical observations in rats and mice included abnormal breathing, sneezing, and thinness, with increasing frequency in higher exposure groups. In rats, clinical observations also included black discoloration of the appendages (pinnae and/or feet), which was noted throughout the study in male and female rats exposed to 3.5 ppm or greater. Clinical observations in mice also included alopecia. Mean body weights of all surviving exposed groups of male rats and 1.75 and 3.5 ppm female rats were significantly less than those of the chamber controls. Mean body weights of all surviving exposed groups of male and female mice were significantly less than those of the chamber controls, and 3.5 ppm males lost weight during the study. In the hematopoietic system of rats, decreases in lymphocyte counts in males and females coincided with increases in neutrophil counts. These alterations in lymphocyte and neutrophil counts were consistent with stress and inflammation. Decreased lymphocyte counts corresponded to lymphoid atrophy in the thymus and spleen. Within the erythron, the erythrocyte counts, hemoglobin concentrations, hematocrit values, and packed cell volumes were significantly elevated in both male and female rats at all time points. Erythron increases at the earlier time points were consistent with a physiological hemoconcentration, while increases at study termination may have been due to hypoxia with a resultant secondary erythrocytosis. In the hematopoietic system of mice, the total leukocyte and lymphocyte counts, as well as neutrophil and eosinophil counts, were increased in males at study termination. Similarly, female mice had increased total leukocyte, neutrophil, and eosinophil counts. The increases in the leukon were generally consistent with inflammation. Hemoglobin concentrations, erythrocyte counts, hematocrit values, and packed cell volumes were decreased in male and female mice. The decreases in the erythron were most likely due to bone marrow suppression as a result of the chronic inflammation in the respiratory tract. Inhalation exposure to Ortho Phthalaldehyde resulted in a spectrum of lesions at sites of contact within the respiratory tract (nose, larynx, trachea, and lung), skin, and eye that were generally consistent with an irritant effect. In general, exposure of rats and mice to Ortho Phthalaldehyde resulted in lesions throughout the respiratory tract that included necrosis, inflammation, regeneration, hyperplasia, and metaplasia, ranging from minimal to moderate in severity. In general, histologic findings occurred at deeper sites within the respiratory tract with increasing exposure concentration. The first site of contact, the nose, was most affected, with many lesions occurring at the lowest exposure concentration (0.44 ppm) in male and female rats and mice. Laryngeal lesions occurred at all exposure concentrations in rats and at 0.88 ppm or greater in mice. Tracheal findings were first noted at a variety of exposure concentrations. Lung findings were most prevalent at the two highest exposure concentrations (3.5 and 7.0 ppm) in rats and mice. In the skin, there were significant increases in adnexa degeneration and epithelial parakeratosis in both male and female rats and mice. In the eye, there were significant increases in suppurative inflammation of the anterior chamber and cornea, as well as corneal necrosis in male and female rats. Rats exposed to Ortho Phthalaldehyde exhibited lower cauda epididymis, epididymis, and testis weights. In rats, total sperm/cauda exhibited a negative trend and sperm motility was lower. There were no histOrtho phthalaldehydethologic correlates identified that could explain the observed responses in sperm parameters, or the weight changes in the testis or epididymis. However, in the higher dose groups where morbidity and mortality were observed, testicular and epididymal histOrtho phthalaldehydethologic lesions were noted. In the testes, these lesions included significant increases in the incidences of elongated spermatid degeneration, apoptosis of the germinal epithelium, and interstitial cell atrophy.
ORTHO PHTHALALDEHYDE

Ortho-phthalaldehyde (OPA) is a chemical compound with the formula C8H6O2.
Ortho phthalaldehyde is a white to pale yellow solid that is commonly used as a disinfectant and sterilant.
Ortho phthalaldehyde is known for its high antimicrobial activity and broad-spectrum efficacy against bacteria, viruses, fungi, and mycobacteria.

CAS Number: 643-79-8
EC Number: 211-745-1



APPLICATIONS


The chemical ortho-phthalaldehyde (OPA) has various applications, including:

Disinfection of medical equipment:
Ortho phthalaldehyde is commonly used in healthcare settings to disinfect and sterilize medical instruments, including endoscopes, surgical tools, and respiratory devices.

High-level disinfection:
Ortho phthalaldehyde is an effective alternative to glutaraldehyde for high-level disinfection processes.
Ortho phthalaldehyde is used to kill or inactivate a wide range of microorganisms, including bacteria, viruses, fungi, and mycobacteria.

Water treatment:
Ortho phthalaldehyde can be utilized in water treatment processes to eliminate harmful microorganisms, ensuring the safety and purity of drinking water.

Industrial applications:
Ortho phthalaldehyde is used in various industrial applications, including oilfield operations, where it can help control microbial growth and prevent biofilm formation.

Surface disinfection:
Ortho phthalaldehyde is effective in disinfecting surfaces in healthcare facilities, laboratories, and other environments where microbial contamination is a concern.

Cold sterilization:
Ortho phthalaldehyde can be used for cold sterilization processes, meaning sterilization can be achieved without the use of heat, making it suitable for temperature-sensitive medical equipment.

Biofilm control:
Ortho phthalaldehyde has been found to be effective in combating biofilm formation, which is a common problem in healthcare settings and industrial environments.

Emerging pathogens:
Ortho phthalaldehyde has been evaluated for its efficacy against emerging pathogens, including SARS-CoV-2, the virus responsible for COVID-19.

Veterinary applications:
Ortho phthalaldehyde can be used in veterinary medicine for disinfection and sterilization of equipment and surfaces.

Laboratory and research applications:
Ortho phthalaldehyde is utilized in laboratories for disinfection of instruments, glassware, and other surfaces to maintain a sterile and controlled environment.

Research and development:
Ortho phthalaldehyde can be used as a chemical reagent in organic synthesis and in the development of new compounds.

Analytical chemistry:
Ortho phthalaldehyde can be employed as a derivatization agent for the analysis of various compounds, including amino acids and carbohydrates, in analytical chemistry techniques such as high-performance liquid chromatography (HPLC) and gas chromatography (GC).

Pharmaceuticals:
Ortho phthalaldehyde may be used in the synthesis of certain pharmaceutical compounds.

Photochemistry:
Ortho phthalaldehyde has been studied for its potential application in photochemical reactions and photodynamic therapy due to its unique chemical properties.

Industrial chemical processes:
Ortho phthalaldehyde can be utilized in certain industrial chemical processes as a reagent or intermediate compound.


Ortho-phthalaldehyde is widely used as a high-level disinfectant for medical instruments in healthcare facilities.
Ortho phthalaldehyde is commonly used for the disinfection and sterilization of endoscopes, ensuring patient safety during medical procedures.

Ortho phthalaldehyde is effective against a broad range of microorganisms, including bacteria, viruses, fungi, and mycobacteria.
Ortho phthalaldehyde is utilized for cold sterilization processes, eliminating the need for heat and preserving the integrity of temperature-sensitive equipment.

Ortho phthalaldehyde finds application in the disinfection of respiratory therapy equipment, including ventilator circuits and face masks.
Ortho phthalaldehyde is used in dental settings for the disinfection and sterilization of dental instruments and equipment.

Ortho phthalaldehyde is employed in laboratories for the disinfection of glassware, surfaces, and equipment to maintain sterile conditions.
In the pharmaceutical industry, Ortho phthalaldehyde may be used in the synthesis of certain pharmaceutical compounds.

Ortho phthalaldehyde can serve as a chemical reagent in research and development activities for organic synthesis.
Ortho phthalaldehyde is utilized as a derivatization agent in analytical chemistry techniques for the analysis of amino acids and carbohydrates.

Ortho phthalaldehyde has been studied for its potential application in photodynamic therapy and photochemical reactions.
In the food industry, Ortho phthalaldehyde may find limited use in equipment disinfection where other disinfectants are not suitable.

Ortho phthalaldehyde can be employed in water treatment processes to control microbial growth and ensure water safety.
Ortho phthalaldehyde may find use in the disinfection of veterinary equipment and surfaces in veterinary clinics.

Ortho phthalaldehyde has been evaluated for its efficacy against emerging pathogens, such as SARS-CoV-2, the virus responsible for COVID-19.
In the research field, OPA can be used as a chemical tool in various experimental setups and protocols.
Ortho phthalaldehyde may have limited applications in certain industrial chemical processes as a reagent or intermediate compound.

Ortho phthalaldehyde can be used for the disinfection and sterilization of tattoo and piercing equipment.
OPA may find limited use in the disinfection of beauty salon tools and equipment.

Ortho phthalaldehyde can be utilized in the disinfection of contact lenses and associated equipment.
Ortho phthalaldehyde is employed in ophthalmology clinics for the disinfection of ophthalmic instruments.

Ortho phthalaldehyde may find use in the disinfection of surgical implants and prosthetic devices.
Ortho phthalaldehyde can be used for the disinfection of catheters and other urinary devices.
Ortho phthalaldehyde may find application in the disinfection of hemodialysis equipment and supplies.
Ortho phthalaldehyde is utilized for the disinfection and sterilization of reusable medical supplies and devices in various healthcare settings.

Ortho phthalaldehyde is used in ambulatory care settings for the disinfection and sterilization of medical devices and equipment used in outpatient procedures.
Ortho phthalaldehyde can be employed in veterinary clinics for the disinfection of veterinary surgical instruments and equipment.

Ortho phthalaldehyde may find application in research laboratories for the disinfection of laboratory animal cages, water systems, and related equipment.
Ortho phthalaldehyde can be used in the biotechnology industry for the disinfection of laboratory-scale bioreactors and associated components.

Ortho phthalaldehyde may be utilized in the pharmaceutical manufacturing industry for the disinfection of small-scale equipment used in drug production.
Ortho phthalaldehyde is employed in research facilities and universities for the disinfection of laboratory hoods, benches, and workspaces.

Ortho phthalaldehyde can be used for the disinfection of post-mortem examination tools and equipment in forensic pathology.
Ortho phthalaldehyde may find application in the disinfection of surgical dressing materials and wound care supplies.
Ortho phthalaldehyde is utilized in assisted living facilities and nursing homes for the disinfection of medical equipment and devices.

Ortho phthalaldehyde can be employed in rehabilitation centers for the disinfection of therapy equipment and devices.
Ortho phthalaldehyde may find use in sports medicine clinics for the disinfection of athletic training equipment and supplies.

Ortho phthalaldehyde is used in dermatology clinics for the disinfection of dermatoscopes and related instruments.
Ortho phthalaldehyde can be employed in fertility clinics for the disinfection of ultrasound probes and fertility treatment equipment.

Ortho phthalaldehyde may find application in podiatry clinics for the disinfection of podiatric instruments and equipment.
Ortho phthalaldehyde is utilized in mobile healthcare units and medical missions for the disinfection of portable medical equipment and supplies.
Ortho phthalaldehyde can be used for the disinfection of chiropractic tables and equipment in chiropractic clinics.

Ortho phthalaldehyde may find use in occupational health settings for the disinfection of occupational therapy and physiotherapy equipment.
Ortho phthalaldehyde is employed in school health services for the disinfection of health office equipment and supplies.

Ortho phthalaldehyde can be utilized in blood banks and transfusion centers for the disinfection of blood collection and processing equipment.
Ortho phthalaldehyde may find application in research facilities for the disinfection of laboratory animal research equipment and facilities.

Ortho phthalaldehyde is used in emergency medical services (EMS) for the disinfection of emergency response equipment and vehicles.
Ortho phthalaldehyde can be employed in dental laboratories for the disinfection of dental prostheses and laboratory instruments.

Ortho phthalaldehyde may find use in eye care clinics for the disinfection of ophthalmic diagnostic equipment and devices.
Ortho phthalaldehyde is utilized in radiology departments for the disinfection of imaging equipment and accessories.
Ortho phthalaldehyde can be used for the disinfection of specialized medical equipment, such as bronchoscopes, gastroscopes, and colonoscopes.



DESCRIPTION


Ortho-phthalaldehyde (OPA) is a chemical compound with the formula C8H6O2.
Ortho phthalaldehyde is a white to pale yellow solid that is commonly used as a disinfectant and sterilant.
Ortho phthalaldehyde is known for its high antimicrobial activity and broad-spectrum efficacy against bacteria, viruses, fungi, and mycobacteria.

Ortho phthalaldehyde is often used in healthcare settings to disinfect medical equipment, such as endoscopes and surgical instruments.
Ortho phthalaldehyde is also used in various industrial applications, including water treatment and oilfield operations.

Ortho-phthalaldehyde is a highly effective disinfectant and sterilant.
Ortho phthalaldehyde is a white to pale yellow solid with a distinctive odor.
Ortho phthalaldehyde has a molecular formula of C8H6O2.

Ortho-phthalaldehyde is soluble in organic solvents like ethanol and acetone.
Ortho phthalaldehyde exhibits broad-spectrum antimicrobial activity against various pathogens.

Ortho phthalaldehyde is commonly used in healthcare settings to disinfect medical equipment.
Ortho phthalaldehyde is particularly effective against bacteria, viruses, fungi, and mycobacteria.

Ortho-phthalaldehyde is an alternative to glutaraldehyde for high-level disinfection.
Ortho phthalaldehyde has a shorter contact time and lower toxicity compared to glutaraldehyde.

Ortho phthalaldehyde is often used to sterilize endoscopes and surgical instruments.
Ortho phthalaldehyde can also be employed in water treatment processes to eliminate harmful microorganisms.
Ortho-phthalaldehyde has been found to be effective against biofilms.

Ortho phthalaldehyde is stable and remains active over a wide range of pH levels.
Ortho phthalaldehyde is not affected by the presence of organic matter.

Ortho-phthalaldehyde is considered less irritating to the skin and respiratory system compared to other disinfectants.
Ortho phthalaldehyde is not classified as a carcinogen by regulatory agencies.

Ortho phthalaldehyde has low volatility, reducing the risk of inhalation exposure.
Ortho-phthalaldehyde has a long shelf life and can be stored for extended periods.

Ortho phthalaldehyde is compatible with a wide range of materials commonly found in healthcare settings.
Ortho phthalaldehyde has been used in various industries, including oilfield operations.

Ortho-phthalaldehyde has been found to be effective against drug-resistant bacteria.
Ortho phthalaldehyde can be used in cold sterilization processes without the need for heat.

Ortho phthalaldehyde has been evaluated for its efficacy against emerging pathogens, such as SARS-CoV-2.
Ortho-phthalaldehyde has been extensively researched and studied for its antimicrobial properties.
Ortho phthalaldehyde continues to be an important tool in infection control and prevention.



PROPERTIES


Chemical formula: C8H6O2
Molecular weight: 134.13 g/mol
Appearance: Colorless to pale yellow liquid
Odor: Characteristic aromatic odor
Melting point: 0-1 °C (32-34 °F)
Boiling point: 282 °C (540 °F)
Density: 1.24 g/cm3
Solubility: Soluble in water, alcohol, and organic solvents
pH: Neutral to slightly acidic
Flash point: 141 °C (286 °F)
Vapor pressure: 1 mmHg at 145 °C (293 °F)
Viscosity: 3.5 cP at 20 °C (68 °F)
Refractive index: 1.588 at 20 °C (68 °F)
Autoignition temperature: 550 °C (1,022 °F)
Stability: Stable under normal conditions
Reactivity: May react with strong oxidizing agents
Flammability: Non-flammable
Toxicity: May cause skin and eye irritation, harmful if swallowed or inhaled
Biodegradability: Biodegradable under certain conditions
Storage conditions: Store in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances
Handling precautions: Use appropriate protective measures, including gloves, goggles, and a lab coat. Avoid contact with skin, eyes, and clothing.
Environmental impact: May be harmful to aquatic organisms. Dispose of properly according to local regulations.
pH stability: Effective at a wide pH range, including acidic and alkaline conditions
Residual activity: Provides residual disinfection properties even after drying
Compatibility: Compatible with a range of materials commonly used in healthcare settings, including stainless steel, aluminum, plastics, and elastomers.



FIRST AID


Inhalation:

Move the affected person to fresh air and ensure they are in a well-ventilated area.
If breathing is difficult, provide oxygen if available and seek immediate medical attention.
If the person is not breathing, perform artificial respiration and seek medical help.


Skin Contact:

Remove contaminated clothing and rinse the affected area with plenty of water for at least 15 minutes.
If irritation or redness occurs, gently wash the area with mild soap and water.
If symptoms persist or if the substance has been absorbed through the skin, seek medical attention.


Eye Contact:

Rinse the eyes gently with lukewarm water for at least 15 minutes, holding the eyelids open to ensure thorough flushing.
Remove contact lenses, if applicable, after rinsing for the first 5 minutes.
Seek immediate medical attention, even if the person does not experience immediate discomfort or pain.


Ingestion:

Rinse the mouth with water and provide the affected person with small sips of water to drink.
Do not induce vomiting unless instructed to do so by medical personnel.
Seek immediate medical attention and provide the medical staff with information about the ingested substance.

Additional First Aid Measures:

If a person has been exposed to a large amount of ortho-phthalaldehyde or exhibits severe symptoms, call emergency services immediately.
Provide comfort and reassurance to the affected person while waiting for medical help.
If possible, have the container or label of the substance available for reference to provide accurate information to medical professionals.
Do not administer any medication or treatment without proper medical guidance.



HANDLING AND STORAGE


Handling Conditions:

Personal Protective Equipment (PPE):
Wear appropriate protective equipment, including chemical-resistant gloves, safety goggles or face shield, and a lab coat or protective clothing, to minimize the risk of exposure.

Ventilation:
Work in a well-ventilated area or use local exhaust ventilation to ensure the dispersal of any potential vapors or fumes.

Avoid Direct Contact:
Avoid direct skin contact with Ortho phthalaldehyde by using proper handling techniques and tools such as pipettes, tongs, or appropriate containers.

Hygiene Practices:
Wash hands thoroughly with soap and water after handling OPA.
Do not eat, drink, or smoke in areas where OPA is handled.


Storage Conditions:

Store in a Cool Area:
Keep Ortho phthalaldehyde in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and open flames.

Temperature Control:
Store at room temperature or below. Avoid exposure to extreme temperatures or rapid temperature changes.

Container Integrity:
Keep Ortho phthalaldehyde in tightly sealed and properly labeled containers to prevent leaks or spills.

Separation from Incompatible Substances:
Store Ortho phthalaldehyde away from oxidizing agents, strong acids, and bases, as well as reactive or incompatible materials.

Secure Storage:
Ensure proper storage conditions to prevent accidental access or use by unauthorized individuals, particularly in settings where Ortho phthalaldehyde may pose a risk.

Protect from Moisture:
Keep Ortho phthalaldehyde containers tightly closed to prevent moisture absorption, as it can affect the quality and stability of the substance.

Separate from Food and Beverages:
Store Ortho phthalaldehyde away from food, beverages, and animal feed to prevent cross-contamination.

Proper Labeling:
Clearly label containers with the name of the substance, hazard symbols, handling precautions, and other relevant information as required by local regulations.

Storage Duration:
Follow the manufacturer's recommendations and local regulations regarding the storage duration of Ortho phthalaldehyde.
Dispose of expired or deteriorated material properly.



SYNONYMS


1,2-Benzenedicarboxaldehyde
1,2-Phthalic aldehyde
Phthalaldehyde
OPA
O-phthalaldehyde
Orthophthalic aldehyde
Benzene-1,2-dicarboxaldehyde
Orthobenzaldehyde
1,2-Benzenedicarbaldehyde
Benzene-1,2-dialdehyde
2-Formylbenzaldehyde
Phthaldehydic acid
Benzene-1,2-diformyl
1,2-Diformylbenzene
Benzene ortho-dialdehyde
Phthaldehydic aldehyde
Benzene-1,2-dicarbonal
1,2-Dicarbonylbenzene
Phthaldialdehyde
OPA-5
1,2-Benzenedicarboxylic aldehyde
2-Formylbenzenecarboxaldehyde
2-Formylbenzaldehyde
o-Phthaldialdehyde
Benzene-o-dialdehyde
2-Phthaldialdehyde
o-Phthaldehyde
Benzene-1,2-dicarbaldehyde
Benzene-1,2-dicarboxylic aldehyde
Benzene-o-diformyl
1,2-Benzenedicarboxyaldehyde
1,2-Diformylbenzene
o-Phthalic aldehyde
2-Formylphthalic acid
Phthalaldehyde-5
Phthalaldehyde-2
Benzene-1,2-diyl-bis-methanol
o-Benzenedicarboxaldehyde
1,2-Benzendicarboxaldehyde
Benzene-o-dicarboxaldehyde
Benzene-1,2-diylaldehyde
o-Phthaldic aldehyde
2-Formylbenzene-1,2-dicarboxaldehyde
Benzene-1,2-diylglycol
Orthophthalaldehyde-5
Phthalaldehyde-ortho
2-Formyl-1,2-benzenedicarboxaldehyde
2-Formyl-1,2-benzenedicarbaldehyde
o-Phthaloylaldehyde
2-Formyl-1,2-dihydroxybenzene
1,2-Benzenedicarbonal
2-Formylphthalic aldehyde
Benzene-o-carbaldehyde
Phthalic aldehyde
Orthobenzoylaldehyde
2-Formyl-1,2-dihydroxybenzene
Benzene-1,2-diformylmethane
Benzene-o-dicarbonal
Orthobenzenedicarbaldehyde
Phthaldehyde-2
2-Formylbenzaldehyde-1,2-dihydrate
Benzene-o-diformylmethane
2-Formylphthalaldehyde
Phthaldic aldehyde
o-Phthalal
1,2-Dihydroxybenzene-2-carbaldehyde
Benzene-o-dicarbonyl
Phthaldic dialdehyde
2-Formylbenzaldehyde-1,2-diol
Benzene-1,2-diyldialdehyde
o-Phthaloylal
2-Formylphthalal
Phthaldialdehyde-2
Benzene-o-dial
1,2-Benzenedicarbal
ORTHO-PHENYL PHENOL (OPP)
Ortho-phenyl phenol (OPP) is a chemical compound with the chemical formula C6H5C6H4OH.
Ortho-phenyl phenol (OPP) is also known by other names such as 2-phenylphenol, biphenylol, or 2-hydroxybiphenyl.
Ortho-phenyl phenol (OPP) is a white crystalline solid that is used for various industrial purposes, including as a fungicide and bactericide.

CAS Number: 90-43-7
EC Number: 201-993-5



APPLICATIONS


Ortho-phenyl phenol (OPP) is extensively used as a fungicide in agriculture.
Ortho-phenyl phenol (OPP) serves as a bactericide, protecting crops from microbial infections.
Ortho-phenyl phenol (OPP) is applied as a preservative for fruits and vegetables during storage and transportation.

In the food industry, OPP acts as a disinfectant, ensuring hygiene and safety.
Ortho-phenyl phenol (OPP) is utilized as a wood preservative to protect against decay and pests.
Ortho-phenyl phenol (OPP) has found applications in the treatment of ornamental plants to prevent fungal growth.

Ortho-phenyl phenol (OPP) has been employed in the preservation of cut flowers, extending their shelf life.
Ortho-phenyl phenol (OPP) is used in the production of certain industrial chemicals and formulations.
In the textile industry, OPP is utilized for mildew control in fabrics and materials.
Ortho-phenyl phenol (OPP) serves as a biocide in cooling water treatment to prevent microbial fouling.

Ortho-phenyl phenol (OPP) has been applied in the manufacture of household disinfectant products.
Ortho-phenyl phenol (OPP) is used as a surface disinfectant in hospitals and other healthcare settings.

Ortho-phenyl phenol (OPP) has been explored for its potential use in controlling post-harvest diseases.
Ortho-phenyl phenol (OPP) is employed in the treatment of seeds to protect against seed-borne pathogens.

Ortho-phenyl phenol (OPP) is used in the leather industry to prevent fungal and bacterial deterioration of hides.
Ortho-phenyl phenol (OPP) has been considered for wood surface treatments in construction materials.
In the cosmetic industry, it may be used as a preservative in certain formulations.

Ortho-phenyl phenol (OPP) has applications in the production of antimicrobial coatings.
Ortho-phenyl phenol (OPP) is utilized in the manufacture of some types of paints and coatings.

Ortho-phenyl phenol (OPP) has been studied for its potential use in controlling microbial contamination in water systems.
Ortho-phenyl phenol (OPP) has applications in the preservation of cultural heritage artifacts.
OPP may be used in the treatment of wood pulp in the paper and pulp industry.

It finds application in the preservation of industrial fluids and lubricants.
The chemical's antimicrobial properties make it useful in various industrial processes.
Research continues to explore new applications and potential alternatives to OPP in various industries.

Ortho-phenyl phenol (OPP) is employed in the horticultural industry to protect greenhouse plants from fungal infections.
Ortho-phenyl phenol (OPP) has been used as a fungicidal treatment for citrus fruits to prevent mold and decay.
In the field of water treatment, OPP may be used as a disinfectant for swimming pools and water reservoirs.

Ortho-phenyl phenol (OPP) has applications in the preservation of wooden utility poles and railway ties.
Ortho-phenyl phenol (OPP) is utilized in the formulation of sanitizing agents for food contact surfaces in processing facilities.
Ortho-phenyl phenol (OPP) finds use in the preservation of stored grains and seeds, preventing contamination by fungi.
Ortho-phenyl phenol (OPP) has been explored for its potential role in controlling mold growth in HVAC systems.

Ortho-phenyl phenol (OPP) may be incorporated into cleaning and hygiene products for its antimicrobial properties.
Ortho-phenyl phenol (OPP) has applications in the treatment of agricultural soil to control soil-borne pathogens.
Ortho-phenyl phenol (OPP) is considered in the development of antifouling coatings for marine structures.

The preservation of historic and archival documents may involve the use of OPP to prevent decay.
In the pharmaceutical industry, OPP may be considered for its antimicrobial role in certain formulations.
Ortho-phenyl phenol (OPP) finds application in the protection of wooden structures in outdoor environments.

Ortho-phenyl phenol (OPP) has been studied for its potential use in the treatment of bacterial and fungal infections in aquaculture.
Ortho-phenyl phenol (OPP) is used in the formulation of wood sealants and stains for added protection.
Ortho-phenyl phenol (OPP) is employed in the manufacturing of household and industrial disinfectant wipes.

Ortho-phenyl phenol (OPP) has been considered for the preservation of wooden musical instruments.
In the poultry industry, it may be used to control microbial contamination in poultry houses.
Ortho-phenyl phenol (OPP) is employed in the treatment of timber used in the construction of outdoor furniture.

Ortho-phenyl phenol (OPP) is used in the preservation of cultural artifacts made from wood, leather, or other susceptible materials.
Ortho-phenyl phenol (OPP) finds applications in the treatment of cooling towers to prevent the growth of harmful microorganisms.
Ortho-phenyl phenol (OPP) may be included in the formulation of antiseptic solutions for medical and veterinary use.
Ortho-phenyl phenol (OPP) has been investigated for its potential role in inhibiting mold growth in building materials.

Ortho-phenyl phenol (OPP) is considered in the development of antimicrobial solutions for the protection of textiles.
Ortho-phenyl phenol (OPP) has been explored for its use in the control of post-harvest diseases in various crops.

Ortho-phenyl phenol (OPP) is utilized in the treatment of wooden utility poles to protect them from fungal decay and extend their lifespan.
In the field of floriculture, OPP is used to prevent mold and microbial growth in flower arrangements and bouquets.

Ortho-phenyl phenol (OPP) finds application in the preservation of wooden fences, decks, and outdoor structures.
Ortho-phenyl phenol (OPP) is considered in the development of antimicrobial coatings for medical devices.
Ortho-phenyl phenol (OPP) has been employed in the formulation of wood varnishes and sealants for both aesthetic and protective purposes.

Ortho-phenyl phenol (OPP) is utilized in the production of fungicidal paints for use in construction and industrial settings.
Ortho-phenyl phenol (OPP) has applications in the treatment of soil used for greenhouse cultivation to control plant pathogens.
In the aerospace industry, OPP may be used to protect certain materials from microbial deterioration.
Ortho-phenyl phenol (OPP) is considered in the formulation of antimicrobial solutions for the treatment of HVAC system components.

Ortho-phenyl phenol (OPP) is used in the preservation of historical wooden structures, such as heritage buildings and monuments.
Ortho-phenyl phenol (OPP) has applications in the treatment of wooden shipping pallets to prevent contamination during transport.
In the automotive industry, OPP may be employed in the preservation of wooden components in vintage and classic cars.

Ortho-phenyl phenol (OPP) finds use in the protection of wooden playground structures to ensure their longevity.
OPP is considered in the development of antimicrobial coatings for textiles and fabrics.
Ortho-phenyl phenol (OPP) has been explored for its potential use in the treatment of waterlogged wooden artifacts recovered from archaeological sites.
Ortho-phenyl phenol (OPP) is used in the preservation of wooden sculptures and carvings in art conservation.

Ortho-phenyl phenol (OPP) finds applications in the treatment of wooden flooring to prevent fungal growth in humid environments.
Ortho-phenyl phenol (OPP) may be included in the formulation of wood treatments for fence posts and poles.
Ortho-phenyl phenol (OPP) is considered in the development of antimicrobial solutions for the protection of leather goods.

In the manufacturing of wooden musical instruments, OPP may be used to prevent microbial damage.
Ortho-phenyl phenol (OPP) is employed in the treatment of wooden beehives to protect against fungal infestations.
Ortho-phenyl phenol (OPP) has applications in the treatment of wooden components in marine structures to prevent degradation.

Ortho-phenyl phenol (OPP) is considered in the formulation of antimicrobial solutions for the protection of outdoor fabrics and upholstery.
Ortho-phenyl phenol (OPP) may find use in the preservation of wooden art installations and sculptures in outdoor settings.
Ortho-phenyl phenol (OPP) is explored for its potential role in the protection of wooden artifacts in museum collections.

Ortho-phenyl phenol (OPP) is utilized in the agricultural sector as a post-harvest treatment for fruits and vegetables to extend shelf life and prevent decay.
Ortho-phenyl phenol (OPP) finds application in the preservation of wooden barrels used for aging and storing wines and spirits.

In the poultry industry, OPP may be used in the sanitation of equipment and facilities to control microbial contamination.
Ortho-phenyl phenol (OPP) is considered in the development of antimicrobial solutions for the treatment of wooden beehives.

Ortho-phenyl phenol (OPP) has applications in the treatment of wooden railway ties to protect against fungal deterioration.
Ortho-phenyl phenol (OPP) may be used in the formulation of wood stains and finishes for both aesthetic and protective purposes.

Ortho-phenyl phenol (OPP) is considered in the development of antimicrobial coatings for industrial equipment and machinery.
In the construction industry, it finds use in the preservation of wooden structures and architectural elements.
Ortho-phenyl phenol (OPP) has applications in the treatment of wooden utility poles used in power distribution.
Ortho-phenyl phenol (OPP) is explored for its potential use in preventing fungal growth in wooden outdoor furniture.

Ortho-phenyl phenol (OPP) may be included in the formulation of wood treatments for the protection of fences and gates.
Ortho-phenyl phenol (OPP) is considered in the preservation of wooden artworks, including sculptures and carvings.
In the textile industry, it may find applications in the development of antimicrobial fabrics.

Ortho-phenyl phenol (OPP) is utilized in the formulation of wood sealants for decks and outdoor structures.
Ortho-phenyl phenol (OPP) has applications in the treatment of wooden packaging materials to prevent contamination during transportation.

Ortho-phenyl phenol (OPP) may be considered in the development of antimicrobial solutions for the protection of antique wooden furniture.
Ortho-phenyl phenol (OPP) is explored for its potential role in controlling microbial contamination in agricultural irrigation systems.
Ortho-phenyl phenol (OPP) finds use in the treatment of wooden components in the manufacturing of musical instruments.

In the preservation of wooden artifacts in museums, OPP may be employed to prevent decay and deterioration.
Ortho-phenyl phenol (OPP) has applications in the treatment of wooden props and sets in the film and theater industry.
Ortho-phenyl phenol (OPP) is considered in the development of antimicrobial solutions for the treatment of wooden cutting boards.

Ortho-phenyl phenol (OPP) may be utilized in the preservation of wooden sculptures and installations in outdoor art exhibitions.
Ortho-phenyl phenol (OPP) finds applications in the treatment of wooden components in the production of outdoor signage.
Ortho-phenyl phenol (OPP) may be included in the formulation of wood treatments for the protection of outdoor structures in parks and recreational areas.
Ortho-phenyl phenol (OPP) is explored for its potential use in the preservation of historical wooden shipwrecks and maritime artifacts.

Biocidal Uses:
Ortho-phenyl phenol (OPP) is approved for use as a biocide in the EEA and/or Switzerland, for: human hygiene, disinfection, veterinary hygiene, food and animals feeds, product preservation, preservation for working / cutting fluids.
Ortho-phenyl phenol (OPP) is being reviewed for use as a biocide in the EEA and/or Switzerland, for: preservation of fibres, leather, rubber, or polymers, preservation for construction materials.

Consumer Uses:
ECHA has no public registered data indicating whether or in which chemical products the substance might be used.
ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.



DESCRIPTION


Ortho-phenyl phenol (OPP) is a chemical compound with the chemical formula C6H5C6H4OH.
Ortho-phenyl phenol (OPP) is also known by other names such as 2-phenylphenol, biphenylol, or 2-hydroxybiphenyl.
Ortho-phenyl phenol (OPP) is a white crystalline solid that is used for various industrial purposes, including as a fungicide and bactericide.

In agricultural applications, OPP has been used as a preservative for fruits, vegetables, and ornamental plants.
Ortho-phenyl phenol (OPP) has fungicidal properties that help protect crops from certain diseases.
Additionally, OPP has been employed as a disinfectant in the food industry and as a wood preservative.
Ortho-phenyl phenol (OPP) is known for its antimicrobial activity against a variety of microorganisms.

However, it's important to note that the use of certain chemical compounds, including OPP, has raised concerns about their potential impact on human health and the environment.
As with any chemical substance, Ortho-phenyl phenol (OPP) is crucial to follow safety guidelines and regulations during its handling and use. Additionally, the approval and regulation of such chemicals may vary by region.

Ortho-phenyl phenol (OPP) is a white crystalline solid.
Ortho-phenyl phenol (OPP) is known for its fungicidal and bactericidal properties.
Ortho-phenyl phenol (OPP) is commonly used as a preservative in the agricultural industry.

Ortho-phenyl phenol (OPP) has a chemical formula of C6H5C6H4OH.
Ortho-phenyl phenol (OPP) is also referred to as 2-phenylphenol or biphenylol.
OPP has been employed in the preservation of fruits and vegetables.
Ortho-phenyl phenol (OPP) acts as a disinfectant in the food industry.

The CAS Registry Number for OPP is 90-43-7.
Its EC Number (EINECS) is 201-993-5.
Ortho-phenyl phenol (OPP) has been utilized as a wood preservative due to its antimicrobial activity.
Ortho-phenyl phenol (OPP) is effective against various microorganisms.

Ortho-phenyl phenol (OPP) is used to protect crops from certain diseases.
Ortho-phenyl phenol (OPP) has been employed in the treatment of ornamental plants.

Ortho-phenyl phenol (OPP) has been a subject of study regarding its environmental impact.
Safety guidelines and regulations must be followed during its handling.
Ortho-phenyl phenol (OPP) has a molecular weight of approximately 170.21 g/mol.

Ortho-phenyl phenol (OPP) has a distinctive aromatic odor.
Ortho-phenyl phenol (OPP) is sparingly soluble in water.
Ortho-phenyl phenol (OPP) is stable under normal conditions of use and storage.
Ortho-phenyl phenol (OPP) can be found in some household disinfectant products.

Ortho-phenyl phenol (OPP) has been used in the production of certain industrial chemicals.
Proper ventilation is recommended when working with OPP.
Ortho-phenyl phenol (OPP) structure includes two phenyl groups.
Ortho-phenyl phenol (OPP) is classified as a hazardous substance, and precautions are necessary.
Research continues to explore its applications and potential alternatives.



PROPERTIES


Chemical Formula: C6H5C6H4OH
Molecular Weight: Approximately 170.21 g/mol
Physical State: White crystalline solid
Odor: Distinctive aromatic odor
Solubility: Sparingly soluble in water
Melting Point: Varies, typically around 57-58°C (135-136°F)
Boiling Point: Approximately 282°C (540°F) at atmospheric pressure
Density: Approximately 1.25 g/cm³
Flash Point: Not applicable or varies depending on formulation
Vapor Pressure: Data may vary based on specific conditions
Stability: Stable under normal conditions of use and storage
pH: Depending on formulation, it may affect the pH of solutions.
Flammability: Generally not considered highly flammable
Toxicity: Can be toxic if ingested or absorbed through the skin; appropriate safety measures are crucial.
Environmental Impact: The environmental impact and persistence may vary; it has been a subject of study and regulation.
Chemical Structure: Contains two phenyl groups and a hydroxyl group.
CAS Registry Number: 90-43-7
EC Number (EINECS): 201-993-5



FIRST AID


Inhalation:

Move to Fresh Air:
If inhaled, immediately move the person to an area with fresh air.

Seek Medical Attention:
If respiratory symptoms persist or if the person has difficulty breathing, seek medical attention.


Skin Contact:

Remove Contaminated Clothing:
Remove any contaminated clothing promptly.

Wash Skin:
Wash the affected skin area with plenty of soap and water.

Seek Medical Attention:
If irritation, redness, or other symptoms persist, seek medical attention.


Eye Contact:

Flush Eyes:
Immediately flush the eyes with gently flowing water for at least 15 minutes, holding the eyelids open.

Seek Medical Attention:
Seek immediate medical attention if irritation or other symptoms persist.


Ingestion:

Do Not Induce Vomiting:
Do not induce vomiting unless directed to do so by medical personnel.

Rinse Mouth:
If the person is conscious, rinse the mouth with water.

Seek Medical Attention:
Seek immediate medical attention, and provide the medical personnel with information about the substance ingested.



HANDLING AND STORAGE


Handling:

Personal Protective Equipment (PPE):
Wear appropriate PPE, including chemical-resistant gloves, safety goggles or face shield, and protective clothing, to prevent skin and eye contact.

Ventilation:
Use in a well-ventilated area or under local exhaust ventilation to control airborne concentrations.

Avoid Contact:
Avoid skin contact and inhalation of vapors or mists.

Hygiene Practices:
Wash hands thoroughly after handling and before eating, drinking, or using the restroom.

Prohibited Activities:
Do not eat, drink, or smoke while handling the substance.

Equipment:
Use equipment made of materials that are compatible with OPP.

Spill Response:
Have spill response measures in place, including absorbent materials and appropriate personal protective equipment.
In the event of a spill, follow established spill response procedures.

Labeling:
Ensure proper labeling of containers, including hazard information and handling precautions.

Training:
Provide training for personnel handling OPP, covering safety procedures, emergency response, and the use of personal protective equipment.


Storage:

Container:
Store OPP in tightly sealed containers made of materials resistant to the substance.

Location:
Store in a cool, dry, well-ventilated area away from incompatible materials.

Temperature:
Store at temperatures recommended by the manufacturer or within specified temperature limits.

Keep Away From:
Keep away from heat sources, open flames, and direct sunlight.

Incompatibilities:
Avoid storing OPP with incompatible substances.
Consult the SDS for information on incompatible materials.

Handling Precautions:
Follow proper handling precautions to prevent spills or leaks during storage.

Segregation:
Segregate from incompatible substances based on storage compatibility.

Fire Precautions:
Implement fire precautions in storage areas. Store away from ignition sources.

Emergency Equipment:
Ensure the availability of emergency equipment, such as eyewash stations and safety showers, in the storage area.

Labeling:
Clearly label storage areas with appropriate hazard information and access restrictions.



SYNONYMS


2-Phenylphenol
Biphenylol
2-Hydroxybiphenyl
Phenyl phenol
o-Phenylphenol
2-Phenylphenoxide
OPP
Dowicide 1
Dowicide O
Dow Biocide O
Orthophenyl phenol
Orthophenyl phenoxide
OPP-35
OPP-40
OPP-65
OPP-H
OPP-O
Phenyl hydroxy diphenyl
Phenylphenol
Phenylphenylol
Sanophen
Sumithion
Terrazol
Dow Biocide
Dowicide
Diphenylol
1-Hydroxy-2-phenylbenzene
1-Phenyl-1,2-dihydroxybenzene
Alpha-phenylphenol
Oxydol
Dowicide 2
Dowicide G
Dowicide G Biocide
Dowicide H
Dowicide M
Dowicide MX
Dowicide W
Phenyl hydroxy diphenyl ether
Phenylphenylene glycol
Phenyl-α-phenylol
Phenylphenol oxides
Phenylphenol, ortho-
2-Hydroxy-1,1'-biphenyl
2-Hydroxydiphenyl
2-Phenyl-1,2-dihydroxybenzene
2-Phenyl-2-hydroxybiphenyl
2-Phenylbiphenylol
Alpha-phenyl-p-phenol
OPP-30
OPP-50
2-Hydroxydiphenyl
2-Phenylphenol, ortho isomer
2-Phenylphenol, O-isomer
Alpha-diphenylol
Alpha-phenyl-p-phenol
Phenol, 2-phenyl-
Phenol, 2-phenyl-, 1:1 mixture with phenol
Phenylphenol (2-phenylphenol)
Phenylphenol (mixed isomers)
Phenylphenol, 2-
Phenylphenol, ortho-
Phenylphenol, pure
Phenylphenol, total
Pure phenylphenol
Diphenylol (ortho-phenylphenol)
Phenylphenol, 2-hydroxy
Phenylphenol, ortho-diphenol
Phenylphenol, ortho-hydroxy
2,2'-Dihydroxydiphenyl
2-Phenylphenol, 95%
2-Phenylphenol, 98%
2-Phenylphenol, extra pure
o-Phenylphenol, 1:1 mixture with phenol
o-Phenylphenol, pure
Total phenylphenol
ORTHO-PHENYLPHENOL (OPP)
Ortho-Phenylphenol (OPP) is white, light yellow to light red powder, slightly phenolic.
Ortho-Phenylphenol (OPP) is almost insoluble in water, soluble in methanol, acetone, benzene, xylene, trichloroethylene, dichlorobenzene and other organic solvents.


CAS Number: 90-43-7
EC Number: 201-993-5
MDL Number: MFCD00002208
E number: E231 (preservatives)
Molecular Formula: C12H10O / C6H5C6H4OH



OPP, Xenol, Torsite, o-Xonal, Remol TRF, FEMA 3959, Orthoxenol, Dowicide 1, 2-Biphenylol, 2-DIPHENYLOL, BIPHENYLOL-2, Tumescal OPE, DOWICIDE 1(R),
Biphenyl-2-ol, BIPHENYL-2-OL, AKOS BAR-1742, 2-PHENYLPHENOL, 2-Phenylphenol, Hydroxdiphenyl, o-phenylphenol, O-Phenyl phenol, Hydroxybiphenyl, 2-Hydroxybiphenyl, 2-HYDROXYDIPHENYL, Preventol O extra, O-HYDROXIDIPHENYL, 1,1'-Biphenyl-2-ol, Ortho Phenylphenol, [1,1'-BIPHENYL]-2-OL, orthohydroxydipbenyl, Hydroxy-2-phenylbenzene, HYDROXY-(2-PHENYL)BENZENE, Dowicide A', (1,1'-Biphenyl)-2-ol, 1-Hydroxy-2-phenylbenzene, 2-Biphenylol, 2-Hydroxybiphenyl, 2-Hydroxydiphenyl, 2-Phenylphenol, Anthrapole 73, Biphenyl, 2-hydroxy-, Biphenyl-2-ol, Dowicide 1, Dowicide 1 antimicrobial,
Invalon OP, Kiwi lustr 277, Nectryl, OPP, Orthohydroxydiphenyl, Orthophenylphenol, Orthoxenol, Phenol, o-phenyl-, Phenyl-2 phenol, Phenylphenol, Preventol O Extra, Remol TRF, Tetrosin OE, Topane, Torsite, Tumescal 0PE, Tumescal OPE, o-Biphenylol, o-Diphenylol, o-Hydroxybiphenyl, o-Hydroxydiphenyl, o-Phenyl phenol, o-Phenylphenol, cosmetic grade, o-Xenol, 2-phenylphenol, o-phenylphenol biphenylol, 2-hydroxybiphenyl, orthophenyl phenol, o-xenol, orthoxenol,
[1,1′-Biphenyl]-2-ol, 2-Phenylphenol, 2-Biphenylol, o-Phenylphenol, Biphenylol, 2-Hydroxybiphenyl, Orthophenyl phenol, o-Xenol, Orthoxenol, 2-Phenylphenol, 2-Hydroxybiphenyl, 90-43-7, O-PHENYLPHENOL, Biphenyl-2-ol, 2-Biphenylol, o-Hydroxybiphenyl, 2-Hydroxydiphenyl, o-Hydroxydiphenyl, Biphenylol, o-Phenyl phenol, Phenylphenol, Orthophenylphenol, Orthoxenol, o-Diphenylol, [1,1'-Biphenyl]-2-ol, Dowicide 1, Torsite, o-Xenol, o-Biphenylol, Preventol O extra,
Orthohydroxydiphenyl, Nectryl, (1,1'-Biphenyl)-2-ol, Tumescal OPE, ortho-Phenylphenol, Remol TRF, Phenol, o-phenyl-, Tetrosin oe, 1-Hydroxy-2-phenylbenzene,
2-Fenylfenol, 2-Hydroxybifenyl, o-Xonal, 2-Phenyl phenol, Biphenyl, 2-hydroxy-, Invalon OP, Anthrapole 73, 2-hydroxy biphenyl, Usaf ek-2219, 1,1'-Biphenyl-2-ol, Dowicide, Kiwi lustr 277, Hydroxdiphenyl, (1,1-Biphenyl)-2-ol, o-Phenylphenol, cosmetic grade, Dowicide 1 antimicrobial, Orthophenyl phenol, orthohydroxydipbenyl, NCI-C50351, Hydroxy-2-phenylbenzene, Nipacide OPP, NSC 1548, 2-Hydroxy-1,1'-biphenyl, 2-Phenylphenol-d5, CHEMBL108829, DTXSID2021151,
CHEBI:17043, D343Z75HT8, NSC-1548, Dowicide A, E231, o-phenylphenate, Phenyl-2 phenol, ortho-phenylphenate, Biphenyl-2-o1, DTXCID201151, Hydroxybiphenyl,
CAS-90-43-7, OPP [pesticide], 2-Phenylphenol [BSI:ISO], CCRIS 1388, 64420-98-0, HSDB 1753, EINECS 201-993-5, EPA Pesticide Chemical Code 064103, BRN 0606907, Stellisept, Manusept, Rotoline, UNII-D343Z75HT8, o-phenyl-phenol, AI3-00062, 2-phenyl-phenol, Tetrosin OE-N, Amocid (TN), MFCD00002208, Preventol 3041, ORTOFENILFENOL, Phenylphenol (ortho-), 2-Phenylphenol, 99%, OPP?, PHENYLPHENOL, O-, WLN: QR BR, ORTHO PHENYL PHENOL, EC 201-993-5, O-PHENYLPHENOL [MI], 2-Phenylphenol, BSI, ISO, SCHEMBL29811, 4-06-00-04579 (Beilstein Handbook Reference), MLS002415765, 2-PHENYLPHENOL [ISO], BIDD:ER0664, O-PHENYLPHENOL [INCI], [1,1''-biphenyl]-2-ol, 2-PHENYLPHENOL [FHFI], 2-PHENYLPHENOL [HSDB], FEMA 3959, 2-Phenylphenol, >=99%, FG, NSC1548, ORTHO-PHENYLPHENOL [IARC], ORTHOPHENYLPHENOL [MART.], ORTHOPHENYLPHENOL [WHO-DD], AMY40390, STR07240, Tox21_202415, Tox21_300674, BDBM50308551, ORTHOPHENYL PHENOL (E 231),
AKOS000118750, PS-8698, NCGC00091595-01, NCGC00091595-02, NCGC00091595-03, NCGC00091595-04, NCGC00091595-05, NCGC00091595-06, NCGC00254582-01, NCGC00259964-01, 2-Phenylphenol 100 microg/mL in Acetone, AC-10362, SMR000778031, 2-Phenylphenol 10 microg/mL in Cyclohexane, 2-Phenylphenol 1000 microg/mL in Acetone,
2-Phenylphenol 10 microg/mL in Acetonitrile, BB 0223993, FT-0654846, P0200, 1,1'-BIPHENYL-2-OL, 2-PHENYLPHENOL, EN300-19380, C02499, D08367, E79453, 2-Phenylphenol, PESTANAL(R), analytical standard, Q209467, SR-01000944520, SR-01000944520-1, W-100332, F0001-2206, Z104473674, InChI=1/C12H10O/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9,13, CH9, O-phenylphenol, 2-hydroxybiphenyl, phenyl-2 phenol, o-xenol, OPP, ortho-phenylphenol, OPP, O-PHENYLPHENOL, Phenylphenol, O-HYDROXYBIPHENYL, BIPHENYL-2-OL, 2-BIPHENYLOL, 2-HYDROXYBIPHENYL, ORTHO-PHENYLPHENOL, o-Xenol, 0-PHENYL PHENOL, o-Phenylphenol, o-Hydroxy biphenyl, Torsite, Xenol, OPP, 2-Biphenylol, o-Hydroxybiphenyl, [1,1'-Biphenyl]-2-ol, 2-Biphenylol, o-Biphenylol, o-Diphenylol, o-Hydroxydiphenyl, o-Phenylphenol, o-Xenol, Biphenyl-2-ol, Dowicide 1, Phenol, o-phenyl-, Preventol O extra, Remol TR, 2-Hydroxybiphenyl, 2-Hydroxydiphenyl, o-Phenylphenol, cosmetic grade, Biphenyl, 2-hydroxy-, NCI-C50351, Torsite, Tumescal OPE, usaf ek-2219, 1-Hydroxy-2-phenylbenzene, 2-Hydroxybifenyl, Dowcide 1, Dowicide 1 antimicrobial, 2-Fenylfenol, Kiwi lustr 277, OPP, Orthohydroxydiphenyl, Orthophenylphenol, Orthoxenol, Tetrosin oe, Nectryl, Anthrapole 73, 2-Hydroxy-1,1'-biphenyl, Invalon OP, Tetrosin OE-N, Biphenylol, Hydroxdiphenyl, Hydroxy-2-phenylbenzene, Hydroxybiphenyl, Nipacide OPP, o-Xonal, Phenylphenol, Xenol, 2-Phenylphenol, (1,1-Biphenyl)-2-ol, Phenylphenol (ortho-), NSC 1548, Preventol 3041, 2-phenylphenol, Anthrapole 73, Biphenyl, 2-hydroxy-, biphenyl-2-o1, Biphenylol, Dowcide 1, Dowcide 1 antimicrobial, o-hydroxybiphenyl, 2-biphenol, collar phenylphenol, 2-hydroxybiphenyl, (1,1-Biphenyl)-2-ol, 1-Hydroxy-2-phenylbenzene, 2-Biphenylol, 2-Fenylfenol, 2-Hydroxy-1,1'-biphenyl, 2-Hydroxybifenyl, 2-Hydroxybiphenyl, 2-Hydroxydiphenyl, 2-Phenyl phenol, 2-Phenylphenol, Anthrapole 73, Biphenyl, 2-hydroxy-, Biphenyl-2-o1, Biphenyl-2-ol, Biphenylol, Dowicide, Dowicide 1, Dowicide 1 antimicrobial, Hydroxdiphenyl, Hydroxy-2-phenylbenzene, Hydroxybiphenyl, Invalon OP, Kiwi lustr 277, Nectryl, Nipacide OPP, o-Biphenylol, o-Diphenylol, o-Hydroxybiphenyl, o-Hydroxydiphenyl, O-phenyl phenol, o-Phenylphenol, o-Phenylphenol, cosmetic grade, o-Xenol, o-Xonal, OPP, Ortho-phenylphenol, Orthohydroxydiphenyl, Orthophenylphenol, Orthoxenol, Phenol, o-phenyl-, Phenyl-2 phenol, Phenylphenol, Preventol O extra, Remol TRF, Tetrosin oe, Tetrosin OE-N, Torsite, Tumescal 0pe, Tumescal OPE, XENOL, Xenol, AI3-00062, BRN 0606907, CASWELL NO. 623AA, CCRIS 1388, EINECS 201-993-5, EPA PESTICIDE CHEMICAL CODE 064103, HSDB 1753, NCI-C50351, NSC 1548, USAF EK-2219, USAF ek-2219,



Ortho-Phenylphenol (OPP) has biocidal properties, making it useful for various preservation applications.
Ortho-Phenylphenol (OPP) is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 to < 10 tonnes per annum.


Ortho-Phenylphenol (OPP) is an organic compound.
In terms of structure, Ortho-Phenylphenol (OPP) is one of the monohydroxylated isomers of biphenyl.
Ortho-Phenylphenol (OPP) is a white solid.


Ortho-Phenylphenol (OPP) is more selective than other free phenols but does produce phytotoxic effects.
Ortho-Phenylphenol (OPP) is more selective than other free phenols butdoes produce phytotoxic effects.
Ortho-Phenylphenol (OPP) is a light lavender crystals or solid.


Ortho-Phenylphenol (OPP) is insoluble in water.
Ortho-Phenylphenol (OPP) is easily soluble in sodium hydroxide solution, ethanol, acetone and other organic solvents, slightly soluble in water.
Ortho-Phenylphenol (OPP) is an organic chemical that is a white, buff, crystalline (sand-like) solid.


In terms of structure, Ortho-Phenylphenol (OPP) is one of the monohydroxylated isomers of biphenyl.
Ortho-Phenylphenol (OPP) is a white solid.
Ortho-Phenylphenol (OPP) is a member of the class of hydroxybiphenyls that is biphenyl substituted by a hydroxy group at position 2.


Ortho-Phenylphenol (OPP) has a role as an environmental food contaminant and an antifungal agrochemical.
Ortho-Phenylphenol (OPP) derives from a hydride of a biphenyl.
Ortho-Phenylphenol (OPP) is a broad-spectrum fungicide used to protect crops in storage.


Ortho-Phenylphenol (OPP) is highly soluble in water, moderately volatile but is not expected to be persistent in the environment.
Ortho-Phenylphenol (OPP) is a broad spectrum fungicide used to protect crops in storage.
Ortho-Phenylphenol (OPP) is highly soluble in water, moderately voatile but is not expected to be persistent in the environment.



USES and APPLICATIONS of ORTHO-PHENYLPHENOL (OPP):
Ortho-Phenylphenol (OPP) is a widely used chemical in the industrial sector that is known for its antimicrobial properties.
Ortho-Phenylphenol (OPP) is a phenolic compound produced through the condensation of phenol and formaldehyde and is commonly used as a preservative in a variety of applications, including wood preservation, cosmetics and personal care products, textiles, paints and coatings, adhesives, and agricultural products.


Ortho-Phenylphenol (OPP) is effective at preventing the growth of bacteria, fungi, and other microorganisms, making it a popular choice for companies looking to ensure the safety and quality of their products.
Ortho-Phenylphenol (OPP) is used for strong sterilization function, as preservative for wood, leather, paper, fruits, vegetables and meat.


Ortho-Phenylphenol (OPP) can be used for hydrophobic synthetic fiber, such as the carrier of chloroprene and dacron carrier dyeing method and the dye intermediate; Or plastic heat stabilizer, surfactant, etc.
Ortho-Phenylphenol (OPP) is mainly used to prepare oil-soluble o-phenylphenol formaldehyde resin in industry.


This resin, Ortho-Phenylphenol (OPP), is used in varnishes with excellent water and alkali stability.
Ortho-Phenylphenol (OPP) is also used as a reagent for the analysis and detection of sugar in bioanalytical chemistry.
Ortho-Phenylphenol (OPP) can also be used in the rubber industry as additives, photographic chemicals.


Ortho-Phenylphenol (OPP) is used for strong bactericidal function, used as wood, leather, paper, as well as preservative preservation of fruits and vegetables, meat preservation.
Wood preservation: Ortho-Phenylphenol (OPP) is commonly used to protect wooden structures such as bridges, poles, and buildings from decay caused by fungi and insects.


Cosmetics and personal care products: Ortho-Phenylphenol (OPP) is used as a preservative in creams, lotions, shampoos, and other similar products to help keep them fresh and free of harmful microorganisms.
Textiles: Ortho-Phenylphenol (OPP) is used in the textile industry to prevent the growth of bacteria and fungi on fabric.


Paints and coatings: Ortho-Phenylphenol (OPP) is added to paint and coatings to prevent the growth of fungi and bacteria on surfaces.
Ortho-Phenylphenol (OPP) is used as a hydrophobic synthetic fiber polyvinyl chloride, polyester and other carriers using carrier staining method, surfactants, bactericidal preservatives, dyes intermediates.


Ortho-Phenylphenol (OPP) is used for strong sterilization function, as preservative for wood, leather, paper, fruits, vegetables and meat.
Ortho-Phenylphenol (OPP) can be used for hydrophobic synthetic fiber, such as the carrier of chloroprene and dacron carrier dyeing method and the dye intermediate; Or plastic heat stabilizer, surfactant, etc.


Ortho-Phenylphenol (OPP) is mainly used to prepare oil-soluble o-phenylphenol formaldehyde resin in industry.
This resin is used in varnishes with excellent water and alkali stability.
Ortho-Phenylphenol (OPP) is also used as a reagent for the analysis and detection of sugar in bioanalytical chemistry.


Ortho-Phenylphenol (OPP) is also used to make dye stuffs and rubber chemicals, but used primarily as a disinfectant cleaner.
Ortho-Phenylphenol (OPP) is used in the manufacture of plastics, resins, rubber, as Agricultural chemical, in making fungicides.
Ortho-Phenylphenol (OPP) is used as an intermediate in making dye stuffs and rubber chemicals; a germicide.


Ortho-Phenylphenol (OPP) is used in food packaging.
Ortho-Phenylphenol (OPP) is a chemical used as a microbicide to control bacteria and viruses, to sanitize fruits, vegetables and eggs, and as a surface disinfectant in hospitals, animal farms, and commercial environments.


Ortho-Phenylphenol (OPP) is used for strong bactericidal function,
used as wood, leather, paper, as well as preservative preservation of fruits and vegetables, meat preservation.
Ortho-Phenylphenol (OPP) can also be used in the rubber industry as additives, photographic chemicals.


Ortho-Phenylphenol (OPP) is used as a hydrophobic synthetic fiber polyvinyl chloride, polyester and other carriers using carrier staining method, surfactants, bactericidal preservatives, dyes intermediates.
Adhesives: Ortho-Phenylphenol (OPP) is used as a preservative in adhesives to prevent the growth of microorganisms and to maintain their effectiveness over time.


Agricultural products: Ortho-Phenylphenol (OPP) is used in agricultural products such as pesticides and herbicides to prevent the growth of fungi and bacteria.
Food preservation: Ortho-Phenylphenol (OPP) is used as a preservative in some food products, such as fruit juices and syrups, to prevent the growth of microorganisms.


Pharmaceuticals: Ortho-Phenylphenol (OPP) can also be used as a preservative in topical medications or creams as well.
Ortho-Phenylphenol (OPP) has high activity and has a broad-spectrum sterilization and mold-removing ability.
Ortho-Phenylphenol (OPP) is a good preservative and can be used for anti-mildew preservation of fruits and vegetables.


Ortho-Phenylphenol (OPP) and its sodium salt can also be used to produce disinfectants and preservatives for fibers and other materials (wood, fabric, paper, adhesives and leather).
Ortho-Phenylphenol (OPP) is used for post-harvest preservation of entire citrus fruits.


Ortho-Phenylphenol (OPP) is used for the manufacture of halogen-free flame retardants for epoxy resins and as functional monomers for optical applications.
Ortho-Phenylphenol (OPP) is mainly used industrially for the preparation of oil-soluble o-phenylphenol formaldehyde resin to produce a varnish excellent in water and alkali stability.


Ortho-Phenylphenol (OPP) is used preservative for the leather industry.
Ortho-Phenylphenol (OPP) is used as antiseptic, printing and dyeing auxiliaries and surfactants, stabilizer and flame retardant for synthesis of new plastics, resins and polymers.


Ortho-Phenylphenol (OPP) is used fluorometric determination of carbohydrate reagents.
Ortho-Phenylphenol (OPP) is widely used in printing and dyeing auxiliaries and surfactants, synthesis of new plastics, resins and polymers stabilizer and flame retardant and other fields.


Ortho-Phenylphenol (OPP) is a widely used organic chemical product, which is widely used in the fields of sterilization and anticorrosion, printing and dyeing auxiliaries and surfactants, synthesis of new plastics, stabilizers and flame retardants of resins and polymer materials.
Ortho-Phenylphenol (OPP) is used broad-spectrum of activity covering bacteria, yeasts, fungi and enveloped viruses.


Ortho-Phenylphenol (OPP) is used for the formulation of all-purpose disinfectants and disinfectant liquid soaps.
Ortho-Phenylphenol (OPP) is used for the preservation of aqueous products such as glues, adhesive dispersions, concrete additives, filler suspensions, pigment slurries and textile print thickeners.


Ortho-Phenylphenol (OPP) is a kind of organic chemical product with a wide range of uses, which is widely used in the fields of sterilization and corrosion prevention, printing and dyeing auxiliaries and surfactants, and the stabilizer and flame retardant of synthetic new plastics, resins and polymer materials.
Ortho-Phenylphenol (OPP) is used active ingredient for disinfectants for use in hospitals, doctor’s offices, industry, institutions, stables and sheds.


Ortho-Phenylphenol (OPP) and its sodium salt have a broad spectrum of sterilization and mildew removal ability, and low toxicity and tasteless, is a better preservative, can be used for the mildew preservation of fruits and vegetables, especially suitable for the mildew prevention of citrus, can also be used to treat lemon, pineapple, pear, peach, tomato, cucumber, can make the decay to a minimum.


In foreign countries, Ortho-Phenylphenol (OPP) and its sodium salt have been widely used in the storage of fruits, vegetables, and meat for anti-corrosion and anti-mold, and have a wide range of uses.
Textiles: Ortho-Phenylphenol (OPP) may be used in textile material production as a dye carrier, especially for synthetic fibers.


Ortho-Phenylphenol (OPP) is a agriculture fungicide and is no longer used as a food additive.
Ortho-Phenylphenol (OPP) is a deoxyribonuclease (DNase) inhibitor with high herbicidal activity, high-efficiency and broad-spectrum sterilization, anti-mildew, disinfection and anti-corrosion capabilities, and low toxicity and tasteless.


Ortho-Phenylphenol (OPP) is generally used as a post-harvest fungicide for citrus fruits.
Ortho-Phenylphenol (OPP) is used as well as disinfectants and anti-mold agents for fibers, protein materials and other materials (wood, fabrics, paper, adhesives and leather, etc.).


When the concentration is 0.005% ~ 0.006%, Ortho-Phenylphenol (OPP) shows a very good bactericidal effect, which is many times greater than that of the lower esters of benzoic acid and p-hydroxybenzoic acid.
Ortho-Phenylphenol (OPP) is also used for the protection of textiles and timber and as a fungistat in water-soluble paints.


Ortho-Phenylphenol (OPP) is remarkably versatile organic chemical products, widely used antiseptic, auxiliaries and surfactant synthesis of new plastics, resins and polymer materials in areas such as stabilizers and flame retardants.
Ortho-Phenylphenol (OPP) is used Fungicide, Disinfectant, Microbiocide.


Ortho-Phenylphenol (OPP) is used for the post-harvest control of storage diseases of apples, citrus fruit, stone fruit, tomatoes, cucumbers and other vegetables.
Ortho-Phenylphenol (OPP) is used to make fungicides.


Ortho-Phenylphenol (OPP) is used Adhesives & Glues,Biocide,Construction Material & Concrete additives, Cosmetics, Carrier / Printing Thickener, Dyes, Flame Retardants, Fungicidal treatments in construction material, Textile Auxiliaries,Treatment of Bitumen Isolation coverings,Plastic additives such as heat stabilizers,Preservation for Whole Citrus Fruits,Rubber chemicals,Wood Preservatives.


Ortho-Phenylphenol (OPP) is used as a dye intermediate, germicide, fungicide, disinfectant, and plasticizer; to manufacture rubber chemicals; in food packaging; as a preservative in water-oil emulsions; antimicrobial preservative in cosmetics.
Ortho-Phenylphenol (OPP) is used as an antimicrobial additive in the manufacture of metalworking fluids, leather, adhesives, and textiles.


Ortho-Phenylphenol (OPP) has a strong bactericidal function, used as wood, leather, paper preservative and fruit and vegetable meat storage preservative.
Ortho-Phenylphenol (OPP) is also used in the production of flame retardants, preservatives, dye carriers, surfactants, dye intermediates, cosmetics and for the production of advanced explosives.


Ortho-Phenylphenol (OPP) is used as a carrier, surfactant, antiseptic and dye intermediate for hydrophobic synthetic fibers such as chlorinated polyamide and polyester.
In Japan, Ortho-Phenylphenol (OPP) and its sodium salt are used for the fungicide of citrus.


In the wax mixed with 0.8% of the goods, the use of spray method in the citrus after harvest, Ortho-Phenylphenol (OPP) can also be used with biphenyl, rot blue to a minimum.
Ortho-Phenylphenol (OPP) is used by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.


Ortho-Phenylphenol (OPP) is approved for use as a biocide in the EEA and/or Switzerland, for: human hygiene, disinfection, veterinary hygiene, food and animals feeds, product preservation, preservation for working / cutting fluids.
Ortho-Phenylphenol (OPP) is being reviewed for use as a biocide in the EEA and/or Switzerland, for: preservation of fibres, leather, rubber, or polymers, preservation for construction materials.


Ortho-Phenylphenol (OPP) is used in the following areas: health services.
Both have been used in agriculture to control fungal and bacterial growth on stored crops, such as fruits and vegetables.
SOPP is applied topically to the crop and then rinsed off, leaving the chemical residue, Ortho-Phenylphenol (OPP).


Most agricultural food applications have been revoked, but Ortho-Phenylphenol (OPP) and SOPP are still used on pears and citrus.
Ortho-Phenylphenol (OPP) is still used as a disinfectant fungicide for industrial applications, on ornamental plants and turfs, in paints, and as a wood preservative.


Ortho-Phenylphenol (OPP) is volatile and has limited water solubility, whereas SOPP is not volatile and is more water soluble.
Both chemicals degrade within hours to weeks in the environment.
In the past, Ortho-Phenylphenol (OPP) was used in home sanitizers for surfaces.


Leathers: Due to its preservative properties, Ortho-Phenylphenol (OPP) is used as an auxiliary to protect leather through various production stages, from hide to finished good.
Other release to the environment of Ortho-Phenylphenol (OPP) is likely to occur from: indoor use as processing aid.


Release to the environment of Ortho-Phenylphenol (OPP) can occur from industrial use: formulation of mixtures.
Ortho-Phenylphenol (OPP) is used for the manufacture of: chemicals.
Release to the environment of Ortho-Phenylphenol (OPP) can occur from industrial use: manufacturing of the substance.


Release to the environment of Ortho-Phenylphenol (OPP) can occur from industrial use: as an intermediate step in further manufacturing of another substance (use of intermediates) and for thermoplastic manufacture.
The primary use of Ortho-Phenylphenol (OPP) is as an agricultural fungicide.


Ortho-Phenylphenol (OPP) is also used for disinfection of seed boxes.
Ortho-Phenylphenol (OPP) is a general surface disinfectant, used in households, hospitals, nursing homes, farms, laundries, barber shops, and food processing plants.


Ortho-Phenylphenol (OPP) can be used on fibers and other materials.
Ortho-Phenylphenol (OPP) is used to disinfect hospital and veterinary equipment.
Other uses of Ortho-Phenylphenol (OPP) are in rubber industry and as a laboratory reagent.


Ortho-Phenylphenol (OPP) is also used in the manufacture of other fungicides, dye stuffs, resins and rubber chemicals.
Ortho-Phenylphenol (OPP) is also used for disinfection of seed boxes.
Cosmetic Uses of Ortho-Phenylphenol (OPP):preservatives


Ortho-Phenylphenol (OPP) is a fungicide used for waxing citrus fruits.
Ortho-Phenylphenol (OPP) is no longer a permitted food additive in the European Union, but is still allowed as a post-harvest treatment in 4 EU countries.
Ortho-Phenylphenol (OPP) is also used for disinfection of seed boxes.


Ortho-Phenylphenol (OPP) is a general surface disinfectant, used in households, hospitals, nursing homes, farms, laundries, barber shops, and food processing plants.
Ortho-Phenylphenol (OPP) can be used on fibers and other materials.


Ortho-Phenylphenol (OPP) is used to disinfect hospital and veterinary equipment.
Other uses of Ortho-Phenylphenol (OPP) are in rubber industry and as a laboratory reagent.
Ortho-Phenylphenol (OPP) is also used in the manufacture of other fungicides, dye stuffs, resins and rubber chemicals.


Ortho-Phenylphenol (OPP) is generally applied post-harvest.
Ortho-Phenylphenol (OPP) is used for post-harvest control of storage disease in apples, citrus fruit, stone fruit, tomatoes, cucumber and peppers through the use of impregnated wrapping materials or by direct application in a wax.


Ortho-Phenylphenol (OPP) is a general surface disinfectant, used in households, hospitals, nursing homes, farms, laundries, barber shops, and food processing plants.
Ortho-Phenylphenol (OPP) can be used on fibres and other materials.


Ortho-Phenylphenol (OPP) is used to disinfect hospital and veterinary equipment.
Other uses of Ortho-Phenylphenol (OPP) are in the rubber industry and as a laboratory reagent.
Ortho-Phenylphenol (OPP) is also used in the manufacture of other fungicides, dyestuff, resins and rubber chemicals.


Leathers: Due to its preservative properties, Ortho-Phenylphenol (OPP) is used as an auxiliary to protect leather through various production stages, from hide to finished good
Textiles: Ortho-Phenylphenol (OPP) may be used in textile material production as a dye carrier, especially for synthetic fibers.


Ortho-Phenylphenol (OPP) is used in food seasonings.
Inhibitory to a wider range of moulds than Biphenyl HMJ12-A.
The practical way of treatment is to immerse citrus fruit in an alkaline aqueous solution of the parent compound or its Na salt.


Ortho-Phenylphenol (OPP) belongs to the family of Biphenyls and Derivatives.
Ortho-Phenylphenol (OPP) is found in low concentrations in some household products such as spray disinfectants and aerosol or spray underarm deodorants.
Ortho-Phenylphenol (OPP) is also used as a fungicide in food packaging and may migrate into the contents.


These are organic compounds containing to benzene rings linked together by a C-C bond.
Ortho-Phenylphenol (OPP) and its water-soluble salt, sodium ortho-phenylphenate (SOPP), are antimicrobial agents used as bacteriostats, fungicides, and sanitizers.


Ortho-Phenylphenol (OPP) is also a commonly used preservative in cosmetics (the dosage is generally 0.05% ~ 0.25%) .
Ortho-Phenylphenol (OPP) can be used for hydrophobic synthetic fibers, such as the carrier and dye intermediate of polyvinyl chloride and polyester carrier dyeing method; it can also be used as heat stabilizer and surfactant for plastics.


Ortho-Phenylphenol (OPP) is mainly used in the industry to prepare oil-soluble o-phenylphenol formaldehyde resin.
Ortho-Phenylphenol (OPP) is the starting material for clear coats with excellent water and alkali stability.


Ortho-Phenylphenol (OPP) is also used as a triose analysis and detection reagent in bioanalytical chemistry; in addition, this product can also be used as an auxiliary agent in the rubber industry and photographic chemicals.


Strong bactericidal function, Ortho-Phenylphenol (OPP) is used as wood, leather, paper preservative and fruit and vegetable meat storage preservative.
Ortho-Phenylphenol (OPP) is also used in the production of flame retardants, preservatives, dye carriers, surfactants, dye intermediates, cosmetics and for the production of advanced explosives.



PREPARATION METHOD OF ORTHO-PHENYLPHENOL (OPP):
using cyclohexanone route to prepare Ortho-Phenylphenol (OPP), namely, using cyclohexanone as raw material, condensation dehydration under acid catalysis to obtain the dimerization Intermediate 2-(1-cyclohexenyl) cyclohexanone and 2-ring hexylene cyclohexanone, O-Phenylphenol was synthesized by dehydrogenation.
a mixture of Ortho-Phenylphenol (OPP) and p-Phenylphenol is obtained from the by-product of phenol production by sulfonation method.

The mixture is heated and dissolved in trichloroethylene, and the crystals of p-Phenylphenol are precipitated by cooling, and then centrifuged and filtered, the solid was dried to give P-Phenylphenol.
The mother liquor was washed with sodium carbonate solution, neutralized with dilute sodium hydroxide and acidified to obtain Ortho-Phenylphenol (OPP).



REACTIVITY PROFILE OF Ortho-Phenylphenol (OPP):
Ortho-Phenylphenol (OPP) react as a weak organic acid.
Ortho-Phenylphenol (OPP) exothermically neutralizes bases.

Ortho-Phenylphenol (OPP) may react with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides to generate flammable gas (H2) and the heat of the reaction may ignite the gas.

Ortho-Phenylphenol (OPP) is sulfonated very readily (for example, by concentrated sulfuric acid at room temperature) in exothermic reactions.
Ortho-Phenylphenol (OPP) may be nitrated very rapidly.
Nitrated phenols often explode when heated and also form metal salts that tend toward detonation by rather mild shock.

Ortho-Phenylphenol (OPP) can react with oxidizing agents .
Ortho-Phenylphenol (OPP) is non flammable.



CHEMICAL PROPERTIES OF Ortho-Phenylphenol (OPP):
Ortho-Phenylphenol (OPP) is a white to buff-colored crystalline solid with a distinct odor.
When heated to decomposition, Ortho-Phenylphenol (OPP) emits acrid smoke and irritating fumes.



PREPARATION OF Ortho-Phenylphenol (OPP):
Ortho-Phenylphenol (OPP) is prepared by condensation of cyclohexanone to give cyclohexenylcyclohexanone.
The latter undergoes dehydrogenation to give Ortho-Phenylphenol (OPP).



PRODUCTION METHODS OF Ortho-Phenylphenol (OPP):
Ortho-Phenylphenol (OPP) is produced as a by-product in the manufacture of diphenyl oxide or by aldol condensation of hexazinone.



PREPARATION OF Ortho-Phenylphenol (OPP):
Ortho-Phenylphenol (OPP) can be recovered from the distillation residue of the process of phenol production via sulfonation.
The phenol distillation residue contains about 40% of phenyl phenol with the other components including phenol, inorganic salts, water and so on.
After vacuum distillation, the mixed Ortho-Phenylphenol (OPP) fraction is separated out with the vacuum being 53.3-66.7kPa.

The temperature, started to be cut at 65-75 ℃ to until 100 ℃ above, but should not higher than 1345 ℃.
Then take advantage of the solubility difference of ortho, p-hydroxy biphenyl in the trichlorethylene, the two are separated into pure product.

The mixed material (mainly Ortho-Phenylphenol (OPP) and 4-hydroxy biphenyl) is heated to be dissolved in the trichlorethylene, after cooling, first precipitate out 4-hydroxy biphenyl crystal.

After centrifuge filtration, dry to obtain 4-hydroxy biphenyl.
The mother liquor was washed with a sodium carbonate solution, followed by dilute alkaline to make the 2-hydroxybiphenyl salt.

After standing stratification, take the upper 2-hydroxybiphenyl sodium salt for dehydration under reduced pressure, namely, sodium salt products.
The 2-hydroxybiphenylsodium salt is white to light red powder, being easily soluble in water with the solubility in 100g of water being 122g.

The pH value of the 2% aqueous solution is 11.1-12.2.
Ortho-Phenylphenol (OPP) is also easily soluble in acetone, methanol, soluble in glycerol, but insoluble in oil.
The sodium salt of Ortho-Phenylphenol (OPP), after acidification, can lead to the formation of Ortho-Phenylphenol (OPP) with both of them being food additives.



PHYSICAL and CHEMICAL PROPERTIES of ORTHO-PHENYLPHENOL (OPP):
CAS Number: 90-43-7
Appearance: White solid, White Crystalline Flakes
Water: 38 mg |-1 at 25 C
Melting point: 56 58 C
Boiling point: 152 154 C at 15mm Hg
Molecular weight: 170.21 g/mol
Flash point: 124 C
Vap.pr.: 15.2 mbar at 163 C
CAS: 90-43-7
EINECS: 201-993-5
InChIKey: LLEMOWNGBBNAJR-UHFFFAOYSA-N
Molecular Formula: C12H10O
Molar Mass: 170.21
Density: 1.21

Melting Point: 57-59°C(lit.)
Boling Point: 282°C(lit.)
Flash Point: 255°F
JECFA Number: 735
Water Solubility: 0.7 g/L (20 ºC)
Solubility: Soluble in ethanol, acetone, benzene,sodium hydroxide,
chloroform, acetonitrile, toluene, hexane, ligroin, ethyl ether, pyridine,
ethylene glycol, isopropanol, glycol ethers and polyglycols.
Vapor Presure: 7 mm Hg ( 140 °C)
Appearance: Crystalline Flakes
Color: White
Merck: 14,7304
BRN: 606907
pKa: 10.01(at 25℃)
PH: 7 (0.1g/l, H2O, 20℃)

Storage Condition: Store below +30°C.
Stability: Stable.
Sensitive: Hygroscopic
Explosive Limit: 1.4-9.5%(V)
Refractive Index: 1.6188 (estimate)
Physical and Chemical Properties:
Melting Point: 57 °c
Boiling Point: 282 ℃
density: 1.213
flash point: 123 ℃
water-soluble:<0.01g/100 mL at 20.5 C

Appearance: bright purple crystals
Appearance: white powder or flake
Assay: 99.5%min
Water: 0.1%max
2-Cyclohexylphenol 0.8% max
Diphenylene oxide : 0.2% max
Sulfate 150 ppm max
melting point : 56-58°C
cas no : 90-43-7
formula : C12H10O
Molar mass : 170.21 g/mol
Density : 1.293 g/cm3
Melting point : 55.5°c

Chemical formula: C12H10O
Molar mass: 170.211 g•mol−1
Density: 1.293 g/cm3
Melting point: 55.5 to 57.5 °C (131.9 to 135.5 °F; 328.6 to 330.6 K)
Boiling point: 280 to 284 °C (536 to 543 °F; 553 to 557 K)
Molecular Weight: 170.21 g/mol
XLogP3: 3.1
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 1
Exact Mass: 170.073164938 g/mol
Monoisotopic Mass: 170.073164938 g/mol
Topological Polar Surface Area: 20.2Ų

Heavy Atom Count: 13
Formal Charge: 0
Complexity: 149
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Physical state: solid
Color: colorless
Odor: No data available
Melting point/freezing point:
Melting point/range: 57 - 59 °C - lit.

Initial boiling point and boiling range: 282 °C - lit.
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits:
Upper explosion limit: 9,5 %(V)
Lower explosion limit: 1,4 %(V)
Flash point: 124 °C - closed cup
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: 0,53 g/l at 20 °C
Partition coefficient: n-octanol/water:

log Pow: 3,18 at 22,5 °C - Bioaccumulation is not expected.
Vapor pressure: 9 hPa at 140 °C
Density: 1,21 g/cm3 at 25 °C
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: none
Other safety information:
Surface tension: 58,72 mN/m at 20,1 °C
Dissociation constant: 9,5 at 20 °C
Melting point: 57-59 °C(lit.)
Boiling point: 282 °C(lit.)
Density: 1.21

vapor pressure: 7 mm Hg ( 140 °C)
refractive index: 1.6188 (estimate)
FEMA: 3959 | 2-PHENYLPHENOL
Flash point: 255 °F
storage temp.: Store below +30°C.
solubility: Soluble in ethanol, acetone, benzene,sodium hydroxide,
chloroform, acetonitrile, toluene, hexane, ligroin, ethyl ether,
pyridine, ethylene glycol, isopropanol, glycol ethers and polyglycols.
form: Crystalline Flakes
pka: 10.01(at 25℃)
color: White
Odor: nearly wh. or lt. buff crystals, mild char. sweetish odor
PH: 7 (0.1g/l, H2O, 20℃)
explosive limit: 1.4-9.5%(V)

Water Solubility: 0.7 g/L (20 ºC)
Sensitive: Hygroscopic
Merck: 14,7304
JECFA Number: 735
BRN: 606907
Stability: Stable.
InChIKey: LLEMOWNGBBNAJR-UHFFFAOYSA-N
LogP: 3.18 at 22.5℃
Substances Added to Food (formerly EAFUS): O-PHENYLPHENOL
FDA 21 CFR: 175.105
CAS DataBase Reference: 90-43-7(CAS DataBase Reference)
EWG's Food Scores: 6-9
FDA UNII: D343Z75HT8
ATC code: D08AE06
Proposition 65 List: o-Phenylphenol
NIST Chemistry Reference: o-Hydroxybiphenyl(90-43-7)
EPA Substance Registry System: 2-Phenylphenol (90-43-7)
Appearance: white to pale purple crystalline powder (est)

Assay: 99.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 57.00 to 59.00 °C. @ 760.00 mm Hg
Boiling Point: 282.00 to 285.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.002020 mmHg @ 25.00 °C. (est)
Flash Point: 255.00 °F. TCC ( 123.89 °C. )
logP (o/w): 3.090
Shelf Life: 24.00 month(s) or longer if stored properly.
Storage: store in cool, dry place in tightly sealed containers, protected from heat and light.
Soluble in: alcohol
water, 535.8 mg/L @ 25 °C (est)
water, 700 mg/L @ 25 °C (exp)
Insoluble in: water
CAS Registry Number: 90-43-7
Classification: Biphenyls and derivatives
Formula: C12H10O
InChI: InChI=1S/C12H10O/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9,13H
InChIKey: LLEMOWNGBBNAJR-UHFFFAOYSA-N
SPLASH: splash10-00xu-3900000000-cc61f48538e181b24290



FIRST AID MEASURES of ORTHO-PHENYLPHENOL (OPP):
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Immediately call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of ORTHO-PHENYLPHENOL (OPP):
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ORTHO-PHENYLPHENOL (OPP):
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ORTHO-PHENYLPHENOL (OPP):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection
Tightly fitting safety goggles
*Skin protection:
Handle with gloves.
Wash and dry hands.
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter type P2
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ORTHO-PHENYLPHENOL (OPP):
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ORTHO-PHENYLPHENOL (OPP):
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .



ORTHO-PHENYLPHENOL (OPP, OR 2-PHENYLPHENOL)
Ortho-phenylphenol (OPP, or 2-phenylphenol) has a molecular structure where a phenolic ring is attached to another phenolic ring through an oxygen bridge.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used for various purposes, including as a disinfectant, fungicide, and bactericide.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has antimicrobial properties, and these characteristics make it suitable for applications in the preservation of certain products.

CAS Number: 90-43-7
Molecular Formula: C12H10O
Molecular Weight: 170.21
EINECS Number: 201-993-5

Ortho-phenylphenol (OPP, or 2-phenylphenol), 2-Hydroxybiphenyl, 90-43-7, O-PHENYLPHENOL, Biphenyl-2-ol, 2-Biphenylol, o-Hydroxybiphenyl, 2-Hydroxydiphenyl, o-Hydroxydiphenyl, Biphenylol, Ortho-phenylphenol (OPP, or 2-phenylphenol), Phenylphenol, Orthophenylphenol, Orthoxenol, o-Diphenylol, [1,1'-Biphenyl]-2-ol, Dowicide 1, Torsite, o-Xenol, o-Biphenylol, Preventol O extra, Orthohydroxydiphenyl, Nectryl, (1,1'-Biphenyl)-2-ol, Tumescal OPE, Ortho-phenylphenol (OPP, or 2-phenylphenol), Remol TRF, Phenol, o-phenyl-, Tetrosin oe, 1-Hydroxy-2-phenylbenzene, 2-Fenylfenol, 2-Hydroxybifenyl, o-Xonal, 2-Phenyl phenol, Biphenyl, 2-hydroxy-, Invalon OP, Anthrapole 73, 2-hydroxy biphenyl, Usaf ek-2219, 1,1'-Biphenyl-2-ol, Dowicide, Kiwi lustr 277, Hydroxdiphenyl, (1,1-Biphenyl)-2-ol, o-Phenylphenol, cosmetic grade, Dowicide 1 antimicrobial, Orthophenyl phenol, orthohydroxydipbenyl, NCI-C50351, Hydroxy-2-phenylbenzene, Nipacide OPP, NSC 1548, 2-Hydroxy-1,1'-biphenyl, Ortho-phenylphenol (OPP, or 2-phenylphenol)-d5, CHEMBL108829, DTXSID2021151, CHEBI:17043, D343Z75HT8, NSC-1548, Dowicide A, E231, o-phenylphenate, Phenyl-2 phenol, ortho-phenylphenate, Biphenyl-2-o1, DTXCID201151, Hydroxybiphenyl, 2-Fenylfenol [Czech], Caswell No. 623AA, 2-Hydroxybifenyl [Czech], CAS-90-43-7, OPP [pesticide], Ortho-phenylphenol (OPP, or 2-phenylphenol) [BSI:ISO], CCRIS 1388, Phenyl-2 phenol [ISO-French], 64420-98-0, HSDB 1753, EINECS 201-993-5, EPA Pesticide Chemical Code 064103, BRN 0606907, Stellisept, Manusept, Rotoline, UNII-D343Z75HT8, o-phenyl-phenol, AI3-00062, 2-phenyl-phenol, Tetrosin OE-N, Amocid (TN), MFCD00002208, Preventol 3041, ORTOFENILFENOL, Phenylphenol (ortho-), Ortho-phenylphenol (OPP, or 2-phenylphenol), 99%, OPP?, PHENYLPHENOL, O-, WLN: QR BR, ORTHO PHENYL PHENOL, EC 201-993-5, O-PHENYLPHENOL [MI], Ortho-phenylphenol (OPP, or 2-phenylphenol), BSI, ISO, SCHEMBL29811, 4-06-00-04579 (Beilstein Handbook Reference), MLS002415765, Ortho-phenylphenol (OPP, or 2-phenylphenol) [ISO], BIDD:ER0664, O-PHENYLPHENOL [INCI], [1,1''-biphenyl]-2-ol, Ortho-phenylphenol (OPP, or 2-phenylphenol) [FHFI], Ortho-phenylphenol (OPP, or 2-phenylphenol) [HSDB], FEMA 3959, Ortho-phenylphenol (OPP, or 2-phenylphenol), >=99%, FG, NSC1548, Ortho-phenylphenol (OPP, or 2-phenylphenol) [IARC], ORTHOPHENYLPHENOL [MART.], ORTHOPHENYLPHENOL [WHO-DD], AMY40390, STR07240, Tox21_202415, Tox21_300674, BDBM50308551, ORTHOPHENYL PHENOL (E 231), AKOS000118750, PS-8698, NCGC00091595-01, NCGC00091595-02, NCGC00091595-03, NCGC00091595-04, NCGC00091595-05, NCGC00091595-06, NCGC00254582-01, NCGC00259964-01, Ortho-phenylphenol (OPP, or 2-phenylphenol) 100 microg/mL in Acetone, AC-10362, SMR000778031, Ortho-phenylphenol (OPP, or 2-phenylphenol) 10 microg/mL in Cyclohexane, Ortho-phenylphenol (OPP, or 2-phenylphenol) 1000 microg/mL in Acetone, Ortho-phenylphenol (OPP, or 2-phenylphenol) 10 microg/mL in Acetonitrile, BB 0223993, FT-0654846, P0200, 1,1'-BIPHENYL-2-OL; Ortho-phenylphenol (OPP, or 2-phenylphenol), EN300-19380, C02499, D08367, E79453, Ortho-phenylphenol (OPP, or 2-phenylphenol), PESTANAL(R), analytical standard, Q209467, SR-01000944520, SR-01000944520-1, W-100332, F0001-2206, Z104473674, InChI=1/C12H10O/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9,13, CH9.

Ortho-phenylphenol (OPP, or 2-phenylphenol) exhibits antimicrobial activity, particularly against bacteria and fungi.
This property has led to its use in agricultural settings, food processing, and as a preservative in some consumer products.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is applied topically to the crop and then rinsed off, leaving the chemical residue, Ortho-phenylphenol (OPP, or 2-phenylphenol).

Most agricultural food applications have been revoked, but Ortho-phenylphenol (OPP, or 2-phenylphenol) and SOPP are still used on pears and citrus (U.S.EPA, 2006).
Ortho-phenylphenol (OPP, or 2-phenylphenol) is still used as a disinfectant fungicide for industrial applications, on ornamental plants and turfs, in paints, and as a wood preservative.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is a member of the class of hydroxybiphenyls that is biphenyl substituted by a hydroxy group at position 2.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is generally used as a post-harvest fungicide for citrus fruits.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has a role as an environmental food contaminant and an antifungal agrochemical.

Ortho-phenylphenol (OPP, or 2-phenylphenol) derives from a hydride of a biphenyl.
Ortho-phenylphenol (OPP, or 2-phenylphenol), also known by its IUPAC name 2-phenylphenol, is a chemical compound with the molecular formula C12H10O.
Ortho-phenylphenol (OPP, or 2-phenylphenol) inhibits the growth of fungi and bacteria.

Ortho-phenylphenol (OPP, or 2-phenylphenol) has a moderate to low toxicity to biodiversity.
The "O-" prefix indicates the position of the phenolic hydroxyl group on the benzene ring.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has a low oral mammalian toxicity, a neurotoxin and is a recognised irritant.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is effective at concentrations as low as 0.05% by weight.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is an ingredient in Lysol® and has been used as a fungicides in Starch, Glue, and Polyvinyl acetate emulsions.
Dilute solutions have also been used for removing lichens from Granite.

Ortho-phenylphenol (OPP, or 2-phenylphenol), the sodium salt of orthOrtho-phenylphenol (OPP, or 2-phenylphenol), is more soluble.
Ortho-phenylphenol (OPP, or 2-phenylphenol) and sodium ortho-phenylphenate (NaOPP) are pesticides used commercially in the food industry that have been shown to be carcinogenic to rat urothelium.
Ortho-phenylphenol (OPP, or 2-phenylphenol) and its water-soluble salt, sodium ortho-phenylphenate (SOPP), are antimicrobial agents used as bacteriostats, fungicides, and sanitizers.

Both have been used in agriculture to control fungal and bacterial growth on stored crops, such as fruits and vegetables.
Ortho-phenylphenol (OPP, or 2-phenylphenol) consists of two phenol groups connected by an oxygen atom.
Ortho-phenylphenol (OPP, or 2-phenylphenol) belongs to the class of organic compounds known as phenols and is specifically classified as a bisphenol.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is highly soluble in water, moderately volatile but is not expected to be persistent in the environment.
Many brands and several voluntary standards limit concentrations of OPP in finished goods, especially in textile articles since there are known safer dye carrier alternatives.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is also known by other names, including phenylphenol, and 2-phenyl phenol.

The chemical formula for Ortho-phenylphenol (OPP, or 2-phenylphenol) is C₆H₅C₆H₄OH.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is a broad spectrum fungicide used to protect crops in storage.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is more selective than other free phenols but does produce phytotoxic effects.

Ortho-phenylphenol (OPP, or 2-phenylphenol), or o-phenylphenol, is an organic compound.
In terms of structure, Ortho-phenylphenol (OPP, or 2-phenylphenol) is one of the monohydroxylated isomers of biphenyl.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is a white solid.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is a biocide used as a preservative with E number E231 and under the trade names Dowicide, Torsite, Fungal, Preventol, Nipacide and many others.
When heated to decomposition, Ortho-phenylphenol (OPP, or 2-phenylphenol) emits acrid smoke and irritating fumes.
In leather, Ortho-phenylphenol (OPP, or 2-phenylphenol) is still a preferred preservative for use during wet blue production, but it should be carefully controlled to minimize final concentrations.

Ortho-phenylphenol (OPP, or 2-phenylphenol) has been found to cause skin changes (discoloration) and irritation to the mucous membranes.
In the past, Ortho-phenylphenol (OPP, or 2-phenylphenol) was used in home sanitizers for surfaces.
This property makes it effective against a range of bacteria and fungi.

In the past, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as a surface disinfectant in the food industry, particularly for the treatment of fruits and vegetables to prevent spoilage and decay during storage and transportation.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been employed as a post-harvest treatment for fruits and vegetables to extend their shelf life by inhibiting the growth of fungi and bacteria.
There have been concerns about the potential health effects of Ortho-phenylphenol (OPP, or 2-phenylphenol), and regulatory agencies have set limits on its use in certain products.

Long-term exposure or exposure at high concentrations may pose health risks, and safety guidelines should be followed.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is efficiently absorbed from the gastrointestinal tract and through the skin, and is eliminated rapidly from the body as OPP glucuronide and sulfate conjugates (Bartels et al., 1998; Cnubben et al. 2002; Timchalk et al., 1998).
Available evidence suggests that Ortho-phenylphenol (OPP, or 2-phenylphenol) does not accumulate in the body; however, small amounts of Ortho-phenylphenol (OPP, or 2-phenylphenol) have been measured in human adipose tissue.

Ortho-phenylphenol (OPP, or 2-phenylphenol) can be synthesized through various methods, including the reaction of phenol with benzene in the presence of catalysts.
The chemical structure of Ortho-phenylphenol (OPP, or 2-phenylphenol) consists of a phenolic ring (phenol) with an additional phenyl group attached to the ortho position, hence the name Ortho-phenylphenol (OPP, or 2-phenylphenol).
Ortho-phenylphenol (OPP, or 2-phenylphenol) exhibits antimicrobial properties by disrupting the cell membranes of microorganisms, leading to their inactivation.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is a broad-spectrum fungicide used to protect crops in storage.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been employed as a preservative in agriculture, particularly for the protection of seeds and crops.
Ortho-phenylphenol (OPP, or 2-phenylphenol) helps prevent the growth of fungi and bacteria that could otherwise damage agricultural products.

In the food industry, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as a preservative on certain fruits and vegetables.
Ortho-phenylphenol (OPP, or 2-phenylphenol) helps extend the shelf life of produce by inhibiting the growth of spoilage microorganisms.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been incorporated into certain disinfectants and cleaning products due to its antimicrobial properties.

Ortho-phenylphenol (OPP, or 2-phenylphenol) contributes to the formulation of products designed to kill or inhibit the growth of bacteria and fungi on surfaces.
The use of Ortho-phenylphenol (OPP, or 2-phenylphenol) in certain applications, especially in the food industry, is subject to regulatory oversight.
Regulatory authorities establish acceptable levels and guidelines to ensure the safety of consumers and the environment.

Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used in various applications, there have been discussions about its potential health and environmental concerns.
As with any chemical, Ortho-phenylphenol (OPP, or 2-phenylphenol) is important to follow recommended guidelines and regulations for safe use.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is highly soluble in water, moderately voatile but is not expected to be persistent in the environment.

Ortho-phenylphenol (OPP, or 2-phenylphenol) has been incorporated into certain disinfectant and cleaner formulations for its antimicrobial properties, contributing to the efficacy of these products.
In the preservation of cultural heritage artifacts, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as a fungicide to protect items susceptible to fungal deterioration.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been employed as an additive in paint and coating formulations to inhibit the growth of fungi and algae on painted surfaces.

Ortho-phenylphenol (OPP, or 2-phenylphenol) has been utilized in certain analytical chemistry techniques.
Ortho-phenylphenol (OPP, or 2-phenylphenol) may be employed in analytical methods for the determination of various substances.
In water treatment processes, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as an antimicrobial agent to control the growth of microorganisms in water systems.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is a synthetic organic compound that belongs to the class of phenols.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is a white to buff-colored crystalline solid with a distinct odor.
In agriculture, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as a fungicide to protect crops from various fungal diseases.

The synthesis of certain dyes may involve Ortho-phenylphenol (OPP, or 2-phenylphenol) as a starting material or intermediate in chemical processes.
Ongoing scientific studies focus on understanding the environmental fate, health impacts, and potential alternatives to Ortho-phenylphenol (OPP, or 2-phenylphenol), contributing to advancements in sustainable and safe practices.
Regulatory agencies conduct risk assessments to evaluate the potential risks associated with the use of Ortho-phenylphenol (OPP, or 2-phenylphenol) in various applications.

This information informs regulatory decisions and guidelines.
Regulations regarding the use of Ortho-phenylphenol (OPP, or 2-phenylphenol) can vary globally.
Different countries may have specific regulations or restrictions on its use in various products.

The primary use of Ortho-phenylphenol (OPP, or 2-phenylphenol) is as an agricultural fungicide.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is generally applied post-harvest.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is a fungicide used for waxing citrus fruits.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is no longer a permitted food additive in the European Union, but is still allowed as a post-harvest treatment in 4 EU countries.
Ortho-phenylphenol (OPP, or 2-phenylphenol) helps prevent the growth of fungi on plants, preserving the quality of crops.
Ortho-phenylphenol (OPP, or 2-phenylphenol) react as a weak organic acid.

May react with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides to generate flammable gas (H2) and the heat of the reaction may ignite the gas.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is sulfonated very readily (for example, by concentrated sulfuric acid at room temperature) in exothermic reactions.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been applied to protect wooden structures, furniture, and utility poles from decay caused by fungi and other microorganisms.

Ortho-phenylphenol (OPP, or 2-phenylphenol) can persist in the environment, and its residues may be detected in soil and water.
This persistence raises environmental considerations and has led to regulatory scrutiny in some regions.

Due to health and environmental concerns, the use of Ortho-phenylphenol (OPP, or 2-phenylphenol) has decreased in certain applications.
In response, industries have sought alternative preservatives and antimicrobial agents.
Ongoing research and development efforts are aimed at finding effective and safer alternatives to Ortho-phenylphenol (OPP, or 2-phenylphenol), especially in areas where its use is restricted.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is volatile and has limited water solubility, whereas SOPP is not volatile and is more water soluble.
General population exposure can occur via dermal, inhalational, or oral routes from residential use and by ingesting treated food or food that was in contact with treated surfaces or equipment.

Ortho-phenylphenol (OPP, or 2-phenylphenol) was detected in 40 of 60 different canned beers at concentrations in the low parts per billion.
Estimated human intakes have been below recommended intake limits.

Melting point: 57-59 °C(lit.)
Boiling point: 282 °C(lit.)
Density: 1.21
vapor pressure: 7 mm Hg ( 140 °C)
refractive index: 1.6188 (estimate)
FEMA: 3959 | Ortho-phenylphenol (OPP, or 2-phenylphenol)
Flash point: 255 °F
storage temp.: Store below +30°C.
solubility: Soluble in ethanol, acetone, benzene,sodium hydroxide, chloroform, acetonitrile, toluene, hexane, ligroin, ethyl ether, pyridine, ethylene glycol, isopropanol, glycol ethers and polyglycols.
form: Crystalline Flakes
pka: 10.01(at 25℃)
color: White
Odor: nearly wh. or lt. buff crystals, mild char. sweetish odor
PH: 7 (0.1g/l, H2O, 20℃)
explosive limit 1.4-9.5%(V)
Water Solubility: 0.7 g/L (20 ºC)
Sensitive: Hygroscopic
Merck: 14,7304
JECFA Number: 735
BRN: 606907
LogP: 3.18 at 22.5℃

Ortho-phenylphenol (OPP, or 2-phenylphenol) is found in low concentrations in some household products such as spray disinfectants and aerosol or spray underarm deodorants.
The sodium salt of orthophenyl phenol, Ortho-phenylphenol (OPP, or 2-phenylphenol), is a preservative, used to treat the surface of citrus fruits.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has found applications in various industrial processes where antimicrobial or preservative properties are desirable.

In healthcare settings, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as a surface disinfectant to maintain a hygienic environment.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is readily degraded in surface waters and municipal waste mixtures, and the degradation is biologically mediated.
Historically, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used in the production of certain photographic chemicals.

Some studies have explored the antiviral properties of Ortho-phenylphenol (OPP, or 2-phenylphenol), though research in this area is ongoing.
While its use has diminished in certain consumer products, Ortho-phenylphenol (OPP, or 2-phenylphenol) may still be present in some formulations, depending on regional regulations and product.
In healthcare settings, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as a surface disinfectant in hospitals and clinics to help control the spread of infections.

Ortho-phenylphenol (OPP, or 2-phenylphenol) has been employed as a mold inhibitor in certain building materials to prevent the growth of mold and mildew.
In river water, radiolabelled 2- phenylphenol at concentrations ranging from 1.2 to 120 μg/litre was degraded to about 50% of the initial concentration in 1 week.
The addition of mercuric chloride to inhibit biological activity reduced the decrease to only 10% after 30 days.

In activated sludge, radiolabelled Ortho-phenylphenol (OPP, or 2-phenylphenol) at 9.6 mg/litre was degraded to 50% of the initial concentration in 24 h.
Ortho-phenylphenol (OPP, or 2-phenylphenol) therefore meets the criteria to be classified as readily biodegradable (FAO/WHO, 1999).
Ortho-phenylphenol (OPP, or 2-phenylphenol) is prepared by condensation of cyclohexanone to give cyclohexenylcyclohexanone.

Ortho-phenylphenol (OPP, or 2-phenylphenol) can be involved in the production of certain thermosetting resins used in various industrial applications.
In aquaculture, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been explored for its potential role in controlling microbial contamination in water systems.

Preparation:
Ortho-phenylphenol (OPP, or 2-phenylphenol) can be recovered from the distillation residue of the process of phenol production via sulfonation.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is also easily soluble in acetone, methanol, soluble in glycerol, but insoluble in oil.

The sodium salt of 2-hydroxy biphenyl, after acidification, can lead to the formation of 2-hydroxy biphenyl with both of them being food additives.
The phenol distillation residue contains about 40% of phenyl phenol with the other components including phenol, inorganic salts, water and so on.
After vacuum distillation, the mixed Ortho-phenylphenol (OPP, or 2-phenylphenol) fraction is separated out with the vacuum being 53.3-66.7kPa.

The latter undergoes dehydrogenation to give Ortho-phenylphenol (OPP, or 2-phenylphenol).
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used in the packaging industry as a surface treatment for packaging materials to prevent the growth of microorganisms on surfaces that come into contact with food.
In addition to its use as a fungicide and antimicrobial agent, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been incorporated into certain biocidal products, contributing to their ability to control or eliminate harmful microorganisms.

In some formulations, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as a component in waterproofing agents for textiles and other materials.
The temperature, started to be cut at 65-75 ℃ to until 100 ℃ above, but should not higher than 1345 ℃.
Then take advantage of the solubility difference of ortho, p-hydroxy biphenyl in the trichlorethylene, the two are separated into pure product.

The mixed material (mainly 2-hydroxy biphenyl and 4-hydroxy biphenyl) is heated to be dissolved in the trichlorethylene, after cooling, first precipitate out 4-hydroxy biphenyl crystal.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has found applications in the pulp and paper industry, where it can be used as a microbiological control agent.

In the conservation and preservation of historic artifacts, Ortho-phenylphenol (OPP, or 2-phenylphenol) may be used in certain treatments to protect items from biological deterioration.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been considered for use in swimming pool water treatment to control microbial growth, although alternative chemicals are often preferred.

Uses:
Ortho-phenylphenol (OPP, or 2-phenylphenol) is used in the manufacture of plastics, resins, rubber, as Agricultural chemical, in making fungicides; as an intermediate in making dye stuffs and rubber chemicals; a germicide; used in food packaging.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is used for strong sterilization function, as preservative for wood, leather, paper, fruits, vegetables and meat.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is remarkably versatile organic chemical products, widely used antiseptic, auxiliaries and surfactant synthesis of new plastics, resins and polymer materials in areas such as stabilizers and flame retardants.
Ortho-phenylphenol (OPP, or 2-phenylphenol) can be used for hydrophobic synthetic fiber, such as the carrier of chloroprene and dacron carrier dyeing method and the dye intermediate; Or plastic heat stabilizer, surfactant, etc.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as a surface disinfectant, particularly in healthcare settings and public spaces, to control the spread of bacteria and viruses.

Ortho-phenylphenol (OPP, or 2-phenylphenol) helps extend the shelf life of fruits and vegetables by preventing the growth of microorganisms that can cause spoilage.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been included in the formulation of certain industrial and household disinfectants to provide antimicrobial properties.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as a treatment to protect fabrics and leather from microbial degradation.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is also used for the protection of textiles and timber and as a fungistat in water-soluble paints.
Ortho-phenylphenol (OPP, or 2-phenylphenol) and its sodium (SOPP) salt have been used world-wide for decades as fungicides and disinfectants.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is used a hydrophobic synthetic fiber polyvinyl chloride, polyester and other carriers using carrier staining method, surfactants, bactericidal preservatives, dyes intermediates.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is also used for disinfection of seed boxes.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is a general surface disinfectant, used in households, hospitals, nursing homes, farms, laundries, barber shops, and food processing plants.
Ortho-phenylphenol (OPP, or 2-phenylphenol) can be used on fibers and other materials.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is used to disinfect hospital and veterinary equipment.
Other uses are in rubber industry and as a laboratory reagent.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is also used in the manufacture of other fungicides, dye stuffs, resins and rubber chemicals.

Ortho-phenylphenol (OPP, or 2-phenylphenol) has been involved in the production of certain photographic chemicals.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as a preservative in some personal care products, such as soaps, deodorants, and lotions.
In addition to its fungicidal properties, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been utilized as a miticide to control mites in agricultural settings.

Ortho-phenylphenol (OPP, or 2-phenylphenol) has been involved in the production of certain thermosetting resins used in the manufacturing of molded products and coatings.
In the aquaculture industry, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been explored for its potential use in controlling microbial contamination in water systems used for fish farming.
In the oil and gas industry, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been investigated for its potential to mitigate bacterial growth in oil wells and related systems.

In controlled environments for biological research, Ortho-phenylphenol (OPP, or 2-phenylphenol) may be used to prevent microbial contamination.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as a surface treatment for certain building materials to prevent the growth of mold and mildew.
Some studies suggest that Ortho-phenylphenol (OPP, or 2-phenylphenol) may exhibit antioxidant properties, and it has been explored as an antioxidant in rubber products.

In the conservation of historic artifacts, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been considered for certain treatments to protect items from biological deterioration.
In agricultural practices, Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as a fogging agent in greenhouses to control the spread of pathogens.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has found applications in various industrial processes where control of microorganisms is essential for production efficiency.

Ortho-phenylphenol (OPP, or 2-phenylphenol) has high activity and has a broad-spectrum sterilization and mold-removing ability.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is a good preservative and can be used for anti-mildew preservation of fruits and vegetables.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is generally used as a hospital and household disinfectant, whereas SOPP is used as a fungicide, which post-harvest treatment of citrus fruits and vegatables for the prevention of mold.

Due to widespread use, including many consumer applications, the fate of Ortho-phenylphenol (OPP, or 2-phenylphenol) in the mammalian organism has been the subject of numerous investigations over many years.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is mainly used to prepare oil-soluble o-phenylphenol formaldehyde resin in industry. This resin is used in varnishes with excellent water and alkali stability.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is also used as a reagent for the analysis and detection of sugar in bioanalytical chemistry.

Ortho-phenylphenol (OPP, or 2-phenylphenol) can also be used in the rubber industry as additives, photographic chemicals.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is not used on growing plants because it is too phytotoxic and there appears to be no information published on its metabolism in plants.

Ortho-phenylphenol (OPP, or 2-phenylphenol) and its sodium salt can also be used to produce disinfectants and preservatives for fibers and other materials (wood, fabric, paper, adhesives and leather).
Ortho-phenylphenol (OPP, or 2-phenylphenol) is mainly used industrially for the preparation of oil-soluble o-phenylphenol formaldehyde resin to produce a varnish excellent in water and alkali stability.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has applications as a fungicide in agriculture to protect crops from fungal infections.

Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as a wood preservative to prevent decay and fungal growth in treated wood products.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used in the past as a preservative in some personal care products, such as soaps, deodorants, and lotions.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has also been used in certain industrial and household disinfectants and cleaning products.

The use of Ortho-phenylphenol (OPP, or 2-phenylphenol) is regulated by health and environmental authorities.
In some regions, its use in certain applications may be restricted or subject to specific concentration limits.
Exposure to high concentrations of Ortho-phenylphenol (OPP, or 2-phenylphenol) can be harmful.

Ortho-phenylphenol (OPP, or 2-phenylphenol)'s important to follow safety guidelines and regulations when handling products containing this compound.
The environmental impact of Ortho-phenylphenol (OPP, or 2-phenylphenol), especially in terms of its persistence and potential for bioaccumulation, is a subject of concern.
Regulations may address its use and disposal to minimize environmental risks.

Due to regulatory and safety considerations, there has been a trend toward finding alternative preservatives, and some industries have moved away from the use of Ortho-phenylphenol (OPP, or 2-phenylphenol) in certain applications.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is used for strong sterilization function, as preservative for wood, leather, paper, fruits, vegetables and meat.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is used as antiseptic, printing and dyeing auxiliaries and surfactants, stabilizer and flame retardant for synthesis of new plastics, resins and polymers.

Fluorometric determination of carbohydrate reagents.
Widely used in printing and dyeing auxiliaries and surfactants, synthesis of new plastics, resins and polymers stabilizer and flame retardant and other fields.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is also used as the sodium and potassium salts where water solublity is important.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is used as a dye intermediate, germicide, fungicide, disinfectant, and plasticizer; to manufacture rubber chemicals; in food packaging; as a preservative in water-oil emulsions; antimicrobial preservative in cosmetics; [HSDB] Used as an antimicrobial additive in the manufacture of metalworking fluids, leather, adhesives, and textiles.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is known for its antimicrobial properties and has been used as a preservative and disinfectant in various products.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is used for strong bactericidal function, used as wood, leather, paper, as well as preservative preservation of fruits and vegetables, meat preservation.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is used for the post-harvest control of storage diseases of apples, citrus fruit, stone fruit, tomatoes, cucumbers and other vegetables.
Ortho-phenylphenol (OPP, or 2-phenylphenol) can be used for hydrophobic synthetic fiber, such as the carrier of chloroprene and dacron carrier dyeing method and the dye intermediate; Or plastic heat stabilizer, surfactant, etc.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is mainly used to prepare oil-soluble o-phenylphenol formaldehyde resin in industry.

This resin is used in varnishes with excellent water and alkali stability.
Ortho-phenylphenol (OPP, or 2-phenylphenol) is also used as a reagent for the analysis and detection of sugar in bioanalytical chemistry.
Ortho-phenylphenol (OPP, or 2-phenylphenol) can also be used in the rubber industry as additives, photographic chemicals.

Ortho-phenylphenol (OPP, or 2-phenylphenol) has been used as a fungicide in agriculture to protect crops from fungal diseases.
Ortho-phenylphenol (OPP, or 2-phenylphenol) helps prevent the growth of molds and fungi on plants.
Ortho-phenylphenol (OPP, or 2-phenylphenol) has been employed as a wood preservative to prevent decay and inhibit the growth of fungi, molds, and insects in treated wood products.

Safety Profile:
Prolonged or repeated exposure to Ortho-phenylphenol (OPP, or 2-phenylphenol) may have adverse effects on health, and chronic exposure has been associated with certain health risks.
Ortho-phenylphenol (OPP, or 2-phenylphenol) can cause irritation to the skin, eyes, and respiratory tract upon contact or inhalation.
O-phenylphenol can cause irritation to the skin and eyes upon direct contact.

Ortho-phenylphenol (OPP, or 2-phenylphenol) is important to use appropriate personal protective equipment (PPE), such as gloves and goggles, to minimize the risk of skin and eye exposure.
This can result in redness, itching, and discomfort.
Some individuals may develop allergic reactions or sensitivities to Ortho-phenylphenol (OPP, or 2-phenylphenol), leading to symptoms such as skin rash or respiratory issues.


ORTHOPHOSPHORIC ACID
O-TOLYL BIGUANIDE, N° CAS : 93-69-6, Nom INCI : O-TOLYL BIGUANIDE. Nom chimique : 1-o-Tolylbiguanide. N° EINECS/ELINCS : 202-268-6. Ses fonctions (INCI), Antioxydant : Inhibe les réactions favorisées par l'oxygène, évitant ainsi l'oxydation et la rancidi
ORTHOPHOSPHOROUS ACID
Orthophosphorous acid, also known as phosphorous acid, is a moderately strong inorganic acid.
Orthophosphorous acid, or phosphorous acid, is a diprotic phosphorus oxoacid that exists as two tautomers while in solution.
Orthophosphorous acid is an intermediate in the preparation of other phosphorus compounds.

CAS Number: 13598-36-2
EC Number: 237-066-7
Molecular formula: H3O3P
Molar mass: 81.99 g/mol

Synonyms: Phosphonic acid, Phosphorous acid, Dihydroxyphosphine oxide, Dihydroxy(oxo)-λ5-phosphane, Dihydroxy-λ5-phosphanone, Orthophosphorous acid, Oxo-λ5-phosphanediol, Oxo-λ5-phosphonous acid, Metaphosphoroic acid

Orthophosphorous acid is the compound described by the formula H3PO3.
Orthophosphorous acid is diprotic (readily ionizes two protons), not triprotic as might be suggested by this formula.
Orthophosphorous acid is an intermediate in the preparation of other phosphorus compounds.

Organic derivatives of Orthophosphorous acid, compounds with the formula RPO3H2, are called Orthophosphorous acids.
The most important use of Orthophosphorous acid is the production of basic lead phosphite, which is a stabilizer in PVC and related chlorinated polymers.
Ferrous materials, including steel, may be somewhat protected by promoting oxidation ("rust") and then converting the oxidation to a metalophosphate by using phosphoric acid and further protected by surface coating.

Orthophosphorous acid, also known as phosphorous acid, is a moderately strong inorganic acid.
Orthophosphorous acid, or phosphorous acid, is a diprotic phosphorus oxoacid that exists as two tautomers while in solution.
Orthophosphorous acid is a pyridinyl biphosphonate bone resorption inhibitor.

Orthophosphorous acid which is also called Orthophosphorous acid is a colourless oxyacids of phosphorus.
Orthophosphorous acid is produced in the form of a white volatile powder by the slow combustion of phosphorus.

Orthophosphorous acid's salts are called phosphates.
Orthophosphorous acid is conveniently prepared by allowing phosphorous trichloride to react with water.

Uses of Orthophosphorous acid:
Orthophosphorous acid is used in the production of basic lead phosphonate PVC stabilizer, aminomethylene Orthophosphorous acid and hydroxyethane diOrthophosphorous acid.
Orthophosphorous acid is used as a strong reducing agent.

Orthophosphorous acid is used in the production of raw materials of phosphorous acid, synthetic fibres and organophosphorus pesticides etc.
Orthophosphorous acid is used in the production of high efficient water treatment agent amino trimethylene Orthophosphorous acid.

Orthophosphorous acid's industrial applications include use in the production of basic lead phosphite and controlling plant diseases.
The most important use of Orthophosphorous acid is the production of phosphites (phosphonates) which are used in water treatment.

Phosphites have shown effectiveness in controlling a variety of plant diseases, in particular, treatment using either trunk injection or foliar containing phosphorous acid salts is indicated in response to infections by phytophthora and pythium-type plant pathogens (both within class oomycetes, known as water molds), such as dieback/root rot and downy mildew.

Orthophosphorous acid is also used for preparing phosphite salts, such as potassium phosphite.
These salts, as well as aqueous solutions of pure Orthophosphorous acid, are fungicides.

Orthophosphorous acid is used primarily for the production of phosphonates and phosphate salts.
These derivatives are used in a number of antimicrobial applications.

In industrial synthesis PCl3 is sprayed into steam at 190oC the heat of reaction is used to distill off the hydrogen chloride and excess water vapour.
Orthophosphorous acid is used as a reagent in the synthesis of Risedronic Acid Sodium Salt.

Orthophosphorous acid is used in the production of basic lead phosphonate PVC stabilizer, aminomethylene Orthophosphorous acid and hydroxyethane diOrthophosphorous acid.
Orthophosphorous acid is also used as a strong reducing agent and in the production of phosphorous acid, synthetic fibres, organophosphorus pesticides, and the highly efficient water treatment agent ATMP.

Chemical Properties Of Orthophosphorous acid:
Orthophosphorous acid has strong reducing properties it tends to be converted to phosphoric acid.

On being heated dry Orthophosphorous acid disproportionates to give phosphine and phosphoric acid.
H3PO3 + 3H3PO3 → PH3 + 3H3PO4

Orthophosphorous acid reacts with a base like sodium hydroxide forms sodium phosphate and water.
H3PO3 + 3NaOH → Na3PO3 + 3H2O

Nomenclature And Tautomerism Of Orthophosphorous acid:
Solid HP(O)(OH)2 has tetrahedral geometry about the central phosphorus atom, with a P–H bond of 132 pm, one P=O double bond of 148 pm and two longer P–OH single bonds of 154 pm.
In common with other phosphorus oxides with P-H bonds (e.g.hypophosphorous acid and dialkyl phosphites), Orthophosphorous acid exists in equilibrium with an extremely minor tautomer P(OH)3. (In contrast, arsenous acid's major tautomer is the trihydroxy form.)

IUPAC recommends that P(OH)3 be called Orthophosphorous acid, whereas the dihydroxy form HP(O)(OH)2 is called Orthophosphorous acid.
Only the reduced phosphorus compounds are spelled with an "ous" ending.
PIII(OH)3 ⇌ HPV(O)(OH)2 K = 1010.3 (25°C, aqueous)

Preparation Of Orthophosphorous acid:

On an industrial scale, the acid is prepared by hydrolysis of phosphorus trichloride with water or steam:
PCl3 + 3 H2O → HPO(OH)2 + 3 HCl

HPO(OH)2 could be produced by the hydrolysis of phosphorus trioxide:
P4O6 + 6 H2O → 4 HPO(OH)2

Reactions Of Orthophosphorous acid:

Acid–base properties:
Phosphorous acid has a pKa in the range 1.26–1.3.
HP(O)(OH)2 → HP(O)2(OH)− + H+ pKa = 1.3

Orthophosphorous acid is a diprotic acid, the hydrogenphosphite ion, HP(O)2(OH)− is a weak acid:
HP(O)2(OH)− → HPO2−3 + H+ pKa = 6.7

The conjugate base HP(O)2(OH)− is called hydrogen phosphite, and the second conjugate base, HPO2−3, is the phosphite ion.
(Note that the IUPAC recommendations are hydrogen phosphonate and phosphonate respectively).

The hydrogen atom bonded directly to the phosphorus atom is not readily ionizable.
Chemistry examinations often test students' appreciation of the fact that not all three hydrogen atoms are acidic under aqueous conditions, in contrast with H3PO4.

Redox Properties Of Orthophosphorous acid:

On heating at 200 °C, Orthophosphorous acid disproportionates to phosphoric acid and phosphine:
4 H3PO3 → 3 H3PO4 + PH3

This reaction is used for laboratory-scale preparations of PH3.

Orthophosphorous acid slowly oxidizes in air to phosphoric acid.
Both Orthophosphorous acid and its deprotonated forms are good reducing agents, although not necessarily quick to react.
They are oxidized to phosphoric acid or its salts.

Orthophosphorous acid reduces solutions of noble metal cations to the metals.

When Orthophosphorous acid is treated with a cold solution of mercuric chloride, a white precipitate of mercurous chloride forms:
H3PO3 + 2 HgCl2 + H2O → Hg2Cl2 + H3PO4 + 2 HCl

Mercurous chloride is reduced further by Orthophosphorous acid to mercury on heating or on standing:
H3PO3 + Hg2Cl2 + H2O → 2 Hg + H3PO4 + 2 HCl

As A Ligand, Orthophosphorous acid:
Upon treatment with metals of d6 configuration, Orthophosphorous acid is known to coordinate as the otherwise rare P(OH)3 tautomer.
Examples include Mo(CO)5(P(OH)3) and [Ru(NH3)4(H2O)(P(OH)3)]2+.

Heating a mixture of potassium tetrachloroplatinate and Orthophosphorous acid gives the luminescent salt potassium diplatinum(II) tetrakispyrophosphite:
2 K2PtCl4 + 8 H3PO3 → K4[Pt2(HO2POPO2H)4] + 8 HCl + 4 H2O

Organic Derivatives Of Orthophosphorous acid:
The IUPAC (mostly organic) name is Orthophosphorous acid.
This nomenclature is commonly reserved for substituted derivatives, that is, organic group bonded to phosphorus, not simply an ester.
For example, (CH3)PO(OH)2 is "methylOrthophosphorous acid", which may of course form "methylphosphonate" esters.

Handling And Storage Of Orthophosphorous acid:

Conditions for safe storage, including any incompatibilities:

Storage conditions:
No metal containers.
Tightly closed.
Dry.
Store under inert gas.
Air sensitive.

Stability And Reactivity Of Orthophosphorous acid:

Reactivity:
No data available

Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature).

Possibility of hazardous reactions:
No data available

Conditions to avoid:
no information available

First Aid Measures of Orthophosphorous acid:

General advice:
First aiders need to protect themselves.

If inhaled:
After inhalation:
Fresh air.
Call in physician.

In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Call a physician immediately.

In case of eye contact:
After eye contact:
Rinse out with plenty of water.

Immediately call in ophthalmologist.
Remove contact lenses.

If swallowed:
After swallowing:
Make victim drink water (two glasses at most), avoid vomiting (risk of perforation).

Call a physician immediately.
Do not attempt to neutralise.

Indication of any immediate medical attention and special treatment needed:
No data available

Fire Fighting Measures of Orthophosphorous acid:

Extinguishing media:

Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.

Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.

Accidental Release Measures of Orthophosphorous acid:

Environmental precautions:
Do not let product enter drains.

Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.

Exposure Controls/personal Protection of Orthophosphorous acid:

Personal protective equipment:

Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles

Skin protection:
Handle with gloves.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min

Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min

Body Protection:
protective clothing

Control of environmental exposure:
Do not let product enter drains.

Identifiers of Orthophosphorous acid:
CAS Number: 13598-36-2
EC Number: 237-066-7
MDL number: MFCD00137258
EC Name: Orthophosphorous acid
Molecular formula: H3O3P

Properties of Orthophosphorous acid:
Chemical formula: H3PO3
Molar mass: 81.99 g/mol
Appearance: white solid deliquescent
Density: 1.651 g/cm3 (21 °C)
Melting point: 73.6 °C (164.5 °F; 346.8 K)
Boiling point: 200 °C (392 °F; 473 K) (decomposes)
Solubility in water: 310 g/100 mL
Solubility: soluble in ethanol
Acidity (pKa): 1.1, 6.7
Magnetic susceptibility (χ): −42.5·10−6 cm3/mol
Odour: Sour odour
Appearance: White solid, deliquescent
Covalently-Bonded Unit: 1
Hydrogen Bond Acceptor: 3
Complexity: 8
Solubility: Soluble in water
Physical state flakes
Color: white
Odor: odorless
Melting point/freezing point:
Melting point/range: 63 - 74 °C at 1.013 hPa

Initial boiling point and boiling range: 259 °C at 1.013 hPa
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: Not applicable
Autoignition temperature: not auto-flammable
Decomposition temperature: No data available
pH: at 20 °C acidic
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: soluble
Partition coefficient: n-octanol/water: Not applicable for inorganic substances
Vapor pressure < 0,1 hPa at 20 °C
Density: 1,651 g/cm3 at 25 °C - lit.
Relative density No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: The product has been shown not to be oxidizing
Other safety information: No data available
OVERBASED CALCIUM SULFONATE (OBCS)
Overbased Calcium Sulfonate (OBCS) is a type of detergent additive commonly used in lubricants, especially in the formulation of engine oils, marine oils, and industrial lubricants.
Overbased Calcium Sulfonate (OBCS) is known for its excellent detergent and dispersant properties, as well as its ability to neutralize acids and provide anti-wear protection.
Overbased Calcium Sulfonate (OBCS) additives in oils are considered potentially critical in driving WEC formations, this ‘driving’ effect being unclear.

CAS Number: 68783-96-0
EINECS Number: 272-213-9

Synonyms: Sulfonic acids, petroleum, calcium salts, overbased, 68783-96-0, DTXSID7028809,EINECS 272-213-9, Petroleum sulfonate, calcium salt, calcium hydroxide and calcium carbonate dispersion.

Overbased Calcium Sulfonate (OBCS)s have long been a widely used thickener for grease applications, but vehicle electrification has led to a dramatic rise in lithium demand in recent years.
Over the long term, grease manufacturers will face supply constraints as supply will be favoring battery manufacturers.
Overbased Calcium Sulfonate (OBCS), extreme pressure, multi-purpose, heavy duty OBCS grease containing unique polymers, anti-wear agents and tackifiers with inherent rust and oxidation resistance to provide the highest performance properties.

The film-forming and friction properties of Overbased Calcium Sulfonate (OBCS) detergents in rolling–sliding, thin film, lubricated contact have been investigated.
All of the commercial detergents studied form thick, solid-like, calcium carbonate films on the rubbed surfaces, of thickness 100–150nm.
The films have a pad-like structure, interspersed by deep valleys in which practically no film is present.

Overbased Calcium Sulfonate (OBCS) has been designed to lubricate under the most severe operating conditions in marine applications and because of its adhesive properties, it effectively stays in place.
In organic chemistry, Overbased Calcium Sulfonate (OBCS) refers to a member of the class of organosulfur compounds with the general formula R−S(=O)2−OH, where R is an organic alkyl or aryl group and the S(=O)2(OH) group a sulfonyl hydroxide.
As a substituent, it is known as a sulfo group.

A sulfonic acid can be thought of as sulfuric acid with one hydroxyl group replaced by an organic substituent.
The parent compound (with the organic substituent replaced by hydrogen) is the parent sulfonic acid, HS(=O)2(OH), a tautomer of sulfurous acid, S(=O)(OH)2.[a] Salts or esters of sulfonic acids are called sulfonates.
Detergents and surfactants are molecules that combine highly nonpolar and highly polar groups.

Traditionally, Overbased Calcium Sulfonate (OBCS)s are the popular surfactants, being derived from fatty acids.
Since the mid-20th century, the usage of sulfonic acids has surpassed soap in advanced societies.
For example, an estimated 2 billion kilograms of Overbased Calcium Sulfonate (OBCS)s are produced annually for diverse purposes.

Lignin sulfonates, produced by sulfonation of lignin are components of drilling fluids and additives in certain kinds of concrete.
Overbased Calcium Sulfonate (OBCS), any of a class of organic acids containing sulfur and having the general formula RSO3H, in which R is an organic combining group.
Overbased Calcium Sulfonate (OBCS)s are among the most important of the organosulfur compounds; the free acids are widely used as catalysts in organic syntheses, while the salts and other derivatives form the basis of the manufacture of detergents, water-soluble dyes and catalysts, sulfonamide pharmaceuticals, and ion-exchange resins.

Overbased Calcium Sulfonate (OBCS)s are particularly useful as intermediates or starting materials in synthesis—for example, in the preparation of phenols.
Overbased Calcium Sulfonate (OBCS)s can greatly enhance the water solubility of compounds, as seen with the sulfonic acid derivative of triphenyl phosphine (TPPTS), P(C6H4-m-SO3Na)3.
Metal complexes of Overbased Calcium Sulfonate (OBCS)s are used as homogeneous catalysts for the syntheses of organic compounds in two-phase systems (e.g., in a mixture of water and an organic solvent) in industry and in the laboratory.

Overbased Calcium Sulfonate (OBCS)s occur naturally—for example, the essential nutrient taurine (2-aminoethanesulfonic acid; NH2CH2CH2SO3H), the sulfobacins and other sulfonolipids (the biologically active products from bacterial cultures that contain 15- to 17-carbon chains attached to the carbon and nitrogen of 2-aminoethanesulfonic acid), and the echinosulfonic acid C (an α-hydroxysulfonic acid containing two brominated indole rings).
The aliphatic sulfonic acids methanesulfonic acid and trifluoromethanesulfonic acid (triflic acid; CF3SO3H) are also commercially important reagents and catalysts.

Overbased Calcium Sulfonate (OBCS), one of the strongest known organic acids, is used as a polymerization catalyst and in fuel cells, in gasoline production, and in the synthesis of organic and organometallic compounds.
Overbased Calcium Sulfonate (OBCS) is a chemical compound—that means it contains at least two different elements combined together.
The main elements in sulfonic acid are sulfur, oxygen, and hydrogen, but the actual formula is more complicated than that.

Because they contain sulfur, sulfonic acids are also called organosulfur compounds.
In general, Overbased Calcium Sulfonate (OBCS)s are very strong acids that come in crystal or liquid form.
They typically don’t have any color and they don’t oxidize, which means that they don’t react with oxygen.

Overbased Calcium Sulfonate (OBCS)s are soluble in water.
These properties make Overbased Calcium Sulfonate (OBCS)s an incredibly useful family of compounds because scientists can control them with ease.
They’re also much less dangerous to use than other acids.

A sustainable and mild one-step strategy is explored for the synthesis of aryl and Overbased Calcium Sulfonate (OBCS)s using a facile combination of halides and sulfur dioxide surrogates under air.
Overbased Calcium Sulfonate (OBCS), also known as sulphonic acids, are a type of organosulfur compound that can be represented by the general formula R−S(=O)2−OH, where R is an alkyl or aryl group in the organic domain, and the S(=O)2(OH) group is a sulfonyl hydroxide moiety.
The sulfo group is another term used to refer to this substituent.

Overbased Calcium Sulfonate (OBCS)s are strongly acidic organosulfur compounds with the general formula R−S(=O)2−OH, where R is an organic alkyl or aryl group.
Applications for sulfonic acids include use as components of dyes, detergents, surfactants, and antibacterial drugs.
The overbasing process involves the formation of micellar structures where calcium carbonate is dispersed in a stable colloidal form.

These micelles are stabilized by the sulfonate molecules, ensuring uniform distribution within the lubricant.
The term “superalkalinity” refers to the high alkalinity reserve provided by these micelles, which is crucial for neutralizing acidic combustion by-products effectively.
Overbased Calcium Sulfonate (OBCS) additives form protective films on metal surfaces, which not only prevent deposits but also provide a physical barrier against wear and corrosion.

In conditions where hydrodynamic lubrication is compromised, such as during startup or under heavy loads, the protective film aids in boundary lubrication, minimizing direct metal-to-metal contact.
Overbased Calcium Sulfonate (OBCS) maintains its efficacy at high temperatures, making it suitable for use in high-performance engines and industrial applications where thermal stability is crucial.
In racing and high-performance automotive engines, OBCS helps maintain engine cleanliness and performance under extreme operating conditions.

Used in commercial trucks and heavy machinery, where high detergency and acid neutralization are vital due to the severe operating conditions and high sulfur content of diesel fuels.
Overbased Calcium Sulfonate (OBCS) is used in formulations designed for extended drain intervals, providing long-lasting protection and stability, which is essential for reducing maintenance costs and downtime.
In hydraulic systems, especially in construction and agricultural machinery, Overbased Calcium Sulfonate (OBCS) helps maintain fluid cleanliness and protect against corrosion and wear.

In marine engines, especially those using high sulfur fuels, the high TBN provided by Overbased Calcium Sulfonate (OBCS) is essential for neutralizing sulfuric acid and preventing corrosive wear.
Overbased Calcium Sulfonate (OBCS) additives are effective in performance, they are generally not biodegradable.
The disposal and potential environmental impact of used lubricants containing OBCS need careful management.

The use of Overbased Calcium Sulfonate (OBCS) in engine oils can indirectly contribute to emission reduction by maintaining engine efficiency and reducing the formation of harmful deposits.
In regions with strict sulfur content regulations, the neutralizing ability of Overbased Calcium Sulfonate (OBCS) is critical.
However, evolving environmental regulations may drive the development of more environmentally friendly alternatives.

Research into incorporating nanoparticles with Overbased Calcium Sulfonate (OBCS) could enhance its performance characteristics, such as improving thermal stability and wear protection.
There is ongoing research into developing biodegradable and more environmentally friendly detergent additives that can match or exceed the performance of traditional Overbased Calcium Sulfonate (OBCS).
Future lubricants may use multi-functional additives that combine the benefits of Overbased Calcium Sulfonate (OBCS) with other performance-enhancing properties, such as friction reduction and oxidation stability.

As emission standards become more stringent, the role of high-performance additives like Overbased Calcium Sulfonate (OBCS) will become even more critical.
However, this may also drive innovation towards cleaner alternatives.
Modern engines equipped with advanced emission control systems, such as Diesel Particulate Filters (DPFs) and Selective Catalytic Reduction (SCR), may require lubricants with lower ash content.

This necessitates careful formulation to balance performance and compatibility.
The production and incorporation of Overbased Calcium Sulfonate (OBCS) additives can be more expensive than other additives, impacting the overall cost of lubricants.
Balancing performance benefits with cost is a significant consideration for lubricant manufacturers.

The availability and cost of raw materials required for producing Overbased Calcium Sulfonate (OBCS) can fluctuate, affecting the consistency and pricing of the final product.
Overbased Calcium Sulfonate (OBCS) is a hypothetical acid with formula H-S(=O)2-OH.
Overbased Calcium Sulfonate (OBCS) is a less stable tautomer of sulfurous acid HO-S(=O)-OH, so sulfonic acid converts rapidly when it is formed.

Derived compounds which replace the sulfur-bonded hydrogen with organic groups are stable.
These may then form salts or esters, called sulfonates.
Overbased Calcium Sulfonate (OBCS)s are a class of organic acids with the general formula R-S(=O)2-OH, where R is usually a hydrocarbon side chain.

Overbased Calcium Sulfonate (OBCS)s are typically much stronger acids than their carboxylic equivalents, and have the unique tendency to bind to proteins and carbohydrates tightly; most "washable" dyes are sulfonic acids (or have the functional sulfonyl group in them) for this reason.
They are also used as catalysts and intermediates for a number of different products.
Overbased Calcium Sulfonate (OBCS) are important as detergents, and the antibacterial sulfa drugs are also sulfonic acid derivatives.

The simplest example is methanesulfonic acid, CH3SO2OH, which is a reagent regularly used in organic chemistry.
Overbased Calcium Sulfonate (OBCS) is also an important reagent.
The primary active ingredient, which acts as a detergent and dispersant.

Present in colloidal form, providing the overbasing characteristic.
Overbased Calcium Sulfonate (OBCS) helps neutralize acidic by-products generated during the operation of engines or machinery.

These ensure the stability and dispersion of the calcium carbonate particles within the lubricant.
The "overbased" term refers to the high base number (BN) or total base number (TBN) of the additive, which is a measure of its capacity to neutralize acids.
Overbased Calcium Sulfonate (OBCS) detergents contain an excess amount of alkaline material, typically calcium carbonate, which enhances their neutralizing capacity.

Overbased Calcium Sulfonate (OBCS)s are sulfonated to produce sulfonic acids.
Overbased Calcium Sulfonate (OBCS)s are neutralized with calcium hydroxide or calcium oxide to form calcium sulfonate.
Overbased Calcium Sulfonate (OBCS) is then overbased by reacting with additional calcium oxide or calcium hydroxide and carbon dioxide, forming a colloidal suspension of calcium carbonate in the sulfonate matrix.

Overbased Calcium Sulfonate (OBCS) helps keep engine parts clean by preventing the formation of deposits and sludge.
The high alkalinity of Overbased Calcium Sulfonate (OBCS) neutralizes acidic by-products from fuel combustion, protecting engine components from corrosion.
Overbased Calcium Sulfonate (OBCS) disperses contaminants and soot particles, keeping them suspended in the oil and preventing them from settling on engine surfaces.

Provides a protective layer on metal surfaces, reducing wear and extending the lifespan of engine components.
Forms a barrier that protects metal surfaces from rust and corrosion.
Overbased Calcium Sulfonate (OBCS) is used in automotive, marine, and stationary engines to improve cleanliness and protect against wear and corrosion.

Utilized in gear oils, hydraulic fluids, and other industrial lubricants where high detergency and acid neutralization are required.
Essential in marine cylinder lubricants, which operate under severe conditions and require high neutralization capacity due to the high sulfur content in marine fuels.
Helps maintain engine cleanliness, improving performance and extending oil change intervals.

Provides anti-wear protection, reducing the rate of engine component wear.
High TBN ensures effective neutralization of acids, protecting engines from corrosive damage.
Effective in a wide range of temperatures and operating conditions.

While Overbased Calcium Sulfonate (OBCS) provides many benefits, it must be balanced with other additives in the lubricant formulation to achieve optimal performance.
Compatibility with other additives and base oils must be carefully considered to avoid issues such as additive dropout or reduced performance.
Overbased Calcium Sulfonate (OBCS) additives can be more expensive than some other detergent types, impacting the overall cost of the lubricant.

Uses:
Overbased Calcium Sulfonate (OBCS) enhances engine cleanliness, reduces wear, and neutralizes acidic by-products, thereby extending oil change intervals and engine life.
Provides superior protection and performance under extreme conditions, maintaining engine cleanliness and efficiency.
Helps withstand severe operating conditions, reducing engine deposits and wear, and prolonging the life of the engine.

Overbased Calcium Sulfonate (OBCS) ensures efficient operation of heavy machinery by maintaining cleanliness and protecting against wear and corrosion.
Essential for neutralizing sulfuric acids in marine engines using high-sulfur fuels, preventing corrosive wear and maintaining engine performance.
Protects large marine engines from corrosion and wear, particularly in slow-speed crosshead engines.

Overbased Calcium Sulfonate (OBCS) is used in gear oils to protect against wear, reduce friction, and prevent deposit formation, ensuring smooth and efficient operation.
Maintains fluid cleanliness, protects against wear and corrosion, and ensures efficient hydraulic system performance.
Enhances the performance and longevity of hydraulic systems in manufacturing and processing equipment.

Provides excellent protection against wear, corrosion, and water washout, making it suitable for use in automotive and industrial applications.
Overbased Calcium Sulfonate (OBCS) enhances lubrication, reduces tool wear, and prevents corrosion, improving the efficiency and lifespan of metalworking tools and machines.
Overbased Calcium Sulfonate (OBCS) is used in turbine oils to provide excellent oxidation stability, protect against corrosion, and ensure efficient operation of power generation equipment.

Enhances performance by maintaining cleanliness, reducing wear, and protecting against oxidation and corrosion in compressor systems.
Overbased Calcium Sulfonate (OBCS) is used to improve the cleanliness, protection, and performance of automatic transmissions, ensuring smooth and reliable operation.
Helps prevent deposit formation and corrosion in fuel systems, ensuring efficient combustion and engine performance.

Overbased Calcium Sulfonate (OBCS) is utilized in oil spill dispersants to break down oil slicks and promote biodegradation, minimizing environmental impact.
Overbased Calcium Sulfonate (OBCS) is used in pulping chemicals to control deposits and scale formation, enhancing the efficiency of the pulping process.
Overbased Calcium Sulfonate (OBCS) is used as a flotation agent in mineral processing to enhance the separation of valuable minerals from ores.

Some food-grade lubricants utilize derivatives of calcium sulfonates due to their non-toxic nature, providing protection against wear and corrosion in food processing equipment.
Formulated into engine cleaners and fuel system cleaners to dissolve and disperse deposits, improving engine performance and fuel efficiency.
Overbased Calcium Sulfonate (OBCS) is used in formulations for high-mileage vehicles to reduce sludge and varnish build-up, improving engine longevity.

Enhances the performance of synthetic motor oils, providing superior protection and extended drain intervals.
Provides robust protection against wear and corrosion in high-revving motorcycle engines.
Overbased Calcium Sulfonate (OBCS) is used in lubricants for off-road vehicles that operate in extreme conditions, ensuring engine cleanliness and reliability.

Essential for fleet maintenance, reducing downtime and maintenance costs by enhancing oil life and engine protection.
Overbased Calcium Sulfonate (OBCS) in metalworking fluids enhances lubrication, reducing friction and heat generation, thus extending tool life and improving surface finish.
Protects high-speed machining centers from wear and corrosion, ensuring precision and efficiency.

Provides superior oxidation stability and deposit control in steam and gas turbines, and in air and gas compressors, ensuring reliable performance.
Overbased Calcium Sulfonate (OBCS) is used in slow-speed crosshead engines where high TBN is crucial for neutralizing sulfuric acid formed from high sulfur content fuels.
Protects medium-speed engines in marine vessels from wear and corrosion, enhancing their operational life.

Formulated into greases for food processing equipment, providing lubrication and protection while meeting stringent safety standards for incidental food contact.
Protects beverage processing machinery from wear and corrosion, ensuring smooth operation and compliance with hygiene standards.
Overbased Calcium Sulfonate (OBCS) is used in wind turbine gear oils to protect gears and bearings from wear and corrosion, ensuring reliable and efficient power generation.

Overbased Calcium Sulfonate (OBCS) enhances the performance of lubricants used in hydroelectric power plants, protecting turbines and other equipment from harsh operating conditions.
Overbased Calcium Sulfonate (OBCS) in hydraulic fluids for excavators provides robust protection against wear, corrosion, and oxidation, ensuring efficient and reliable operation.
Overbased Calcium Sulfonate (OBCS) is used in lubricants for drilling equipment, providing protection against extreme pressures and harsh environmental conditions.

Protects textile machinery from wear and corrosion, enhancing efficiency and longevity, and reducing maintenance costs.
Reduces friction between moving parts, improving efficiency and reducing energy consumption.
Maintains performance under a wide range of temperatures, from low startup temperatures to high operating temperatures.

Forms a protective layer on metal surfaces, reducing wear and extending the life of equipment components.
Provides superior protection against rust and corrosion, particularly in harsh and corrosive environments.
Prevents the formation of deposits, sludge, and varnish, maintaining cleanliness and efficient operation of engines and machinery.

High TBN ensures effective neutralization of acids, protecting engines and machinery from corrosive damage.
Indirectly contributes to reduced emissions by maintaining engine and machinery efficiency, leading to better fuel economy and lower exhaust emissions.
Efforts are ongoing to develop biodegradable derivatives of calcium sulfonate to reduce environmental impact.

Development of environmentally friendly and biodegradable alternatives to traditional OBCS additives.
Research into sourcing raw materials from renewable resources to reduce environmental footprint.
Incorporating nanoparticles with OBCS to enhance properties such as thermal stability, wear protection, and friction reduction.

Creating multi-functional additives that offer comprehensive protection and performance benefits.
Developing specialized lubricants for EV powertrains that require unique properties compared to traditional internal combustion engines.
Exploring applications in aerospace lubricants where extreme operating conditions demand superior performance.

Meeting stringent emission standards and regulations by developing low-ash and low-sulfur formulations.
Ensuring that new formulations comply with health and safety regulations, particularly in food-grade and pharmaceutical applications.

Safety Profile:
Direct contact with Overbased Calcium Sulfonate (OBCS) can cause irritation to the skin and eyes.
Symptoms may include redness, itching, and burning sensations. Prolonged or repeated exposure can lead to dermatitis or eye irritation.
Overbased Calcium Sulfonate (OBCS) dust or aerosols may cause respiratory irritation, coughing, or difficulty breathing.

This risk is typically low under normal handling conditions but may increase in poorly ventilated areas or during activities that generate airborne particles.
Overbased Calcium Sulfonate (OBCS) may result in gastrointestinal irritation, nausea, vomiting, and diarrhea.
Ingestion should be avoided, and medical attention sought if ingestion occurs accidentally.

Overbased Calcium Sulfonate (OBCS) itself is not considered highly toxic, it may contain impurities or additives that could pose health risks if ingested, inhaled, or absorbed through the skin.
Methanol or other chemical residues from the manufacturing process could be harmful if present.


OXALALDEHYDE
OXALALDEHYDE = GLYOXAL = ETHANEDIAL


CAS Number: 107-22-2
EC Number: 203-474-9
MDL number: MFCD00006957
Molecular Formula: C2H2O2 or OHCCHO


Oxalaldehyde is the dialdehyde that is the smallest possible and which consists of ethane having oxo groups on both carbons.
Oxalaldehyde has a role as a pesticide, an agrochemical, an allergen and a plant growth regulator.
Oxalaldehyde is a natural product found in Sesamum indicum with data available.
Oxalaldehyde appears as yellow crystals melting at15 °C.


Hence often encountered as a light yellow liquid with a weak sour odor.
Oxalaldehyde's vapor has a green color and burns with a violet flame.
Oxalaldehyde is an organic compound with the chemical formula OCHCHO.
Oxalaldehyde is the smallest dialdehyde (a compound with two aldehyde groups).


Oxalaldehyde is a crystalline solid, white at low temperatures and yellow near the melting point (15 °C).
Oxalaldehyde's liquid is yellow, and the vapor is green.
Oxalaldehyde is not commonly encountered because it is usually handled as a 40% aqueous solution (density near 1.24 g/mL).
Oxalaldehyde forms a series of hydrates, including oligomers.


For many purposes, these hydrated oligomers behave equivalently to Oxalaldehyde.
Oxalaldehydeis produced industrially as a precursor to many products.
Oxalaldehyde is a valuable building block in organic synthesis, especially in the synthesis of heterocycles such as imidazoles.
A convenient form of the reagent for use in the laboratory is Oxalaldehyde's bis(hemiacetal) with ethylene glycol, 1,4-dioxane-2,3-diol.


Oxalaldehyde is commercially available.
Oxalaldehyde condenses with urea to afford 4,5-dihydroxy-2-imidazolidinone, which further reacts with formaldehyde to give the bis(hydroxymethyl) derivative dimethylol ethylene urea, which is used for wrinkle-resistant chemical treatments of clothing, i.e. permanent press.
Oxalaldehyde is an organic compound with the formula C2H2O2, With a molecular weight of 58.036.


Oxalaldehyde's appearance is white or gray-white crystalline powder (yellow angular or irregular sheet, become white after cooling), used as pharmaceutical intermediates, fabric finishing agents, dyes and dye intermediates.
Oxalaldehyde's vapor is green and burns with a purple flame.
Rapid polymerization when placed, placed in water (violent reaction), or dissolved in water-containing solvents.


Oxalaldehyde usually exist in various aggregate forms.
The anhydrous polymer then transforms into a monomer upon heating.
Heat the polymer with antipropylene anisane, phenyl ether, yellow camphor, methyl, nonylketone, or benzaldehyde.
Aqueous solution contains single-molecule Oxalaldehyde, which is weakly acidic and chemically active, and can add or condense with ammonia, amide, aldehyde, and compounds containing carboxyl groups.


Oxalaldehyde is the raw material for organic synthesis.
2D-resin is obtained by heating and condensation of ethylene formaldehyde and urea in the presence of sodium carbonate, which is used as fabric finishing agent.
Oxalaldehyde reacts with formaldehyde and ammonium sulfate to synthesize imidazole.


Oxalaldehyde is an intermediate of anti-tuberculosis drug pyrazinamide.
Oxalaldehyde is an organic compound with the formula C2H2O2, With a molecular weight of 58.036.
Oxalaldehyde's appearance is white or gray-white crystalline powder (yellow angular or irregular sheet, become white after cooling), used as pharmaceutical intermediates, fabric finishing agents, dyes and dye intermediates.


Oxalaldehyde is colorless or light yellow liquid, soluble in water, ether and ethanol.
The chemical property of Oxalaldehyde is very active and easy to polymerize into white resin like solid.
Oxalaldehyde can form acetals with compounds containing hydroxyl groups.
Oxalaldehyde is an organic compound with the chemical formula OCHCHO.


Oxalaldehyde is a yellow-colored liquid that evaporates to give a green-colored gas.
Oxalaldehyde is the smallest dialdehyde (two aldehyde groups).
Oxalaldehyde's structure is more complicated than typically represented because the molecule hydrates and oligomerizes.
Oxalaldehyde is produced industrially as a precursor to many products.


Oxalaldehyde is an organic compound with the formula OCHCHO.
Oxalaldehyde is a yellow-colored liquid that evaporates to give a green-colored gas.
Oxalaldehyde is the smallest dialdehyde (two aldehyde groups).
Oxalaldehyde's structure is more complicated than typically represented because the molecule hydrates and oligomerizes.


Oxalaldehyde is produced industrially as a precursor to many products.
Oxalaldehyde is suitable for nucleic acid denaturation, and binding of DNA/RNA to nitrocellulose membrane.
Oxalaldehyde is a crosslinking agent used in protein and carbohydrate chemistry when linking together monomer units.
Oxalaldehyde, also known as 1,2-ethanedione or oxalaldehyde, is a member of the class of compounds known as short-chain aldehydes.


Short-chain aldehydes are an aldehyde with a chain length containing between 2 and 5 carbon atoms.
Oxalaldehyde is soluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa).
Oxalaldehyde is an organic compound with the chemical formula OCHCHO.
Oxalaldehyde is a yellow-colored liquid that evaporates to give a green-colored gas.


Oxalaldehyde is the smallest dialdehyde (two aldehyde groups).
Oxalaldehyde's structure is more complicated than typically represented because the molecule hydrates and oligomerizes.
Oxalaldehyde is produced industrially as a precursor to many products .
Oxalaldehyde is commercially available as a 40% aqueous solution, clear to slightly yellow with a faint, sour odor; Yellow solid that turns white on cooling; Vapors are green; mp = 15 deg C; Liquid; Yellow solid below 15 deg C.


Oxalaldehyde is colourless or light yellow liquid.
Oxalaldehyde that is the smallest possible and which consists of ethane having oxo groups on both carbons.
Oxalaldehyde is yellow crystals melting at15°C.
Hence often encountered as a light yellow liquid with a weak sour odor.
Oxalaldehyde's vapor has a green color and burns with a violet flame.



USES and APPLICATIONS of OXALALDEHYDE:
Cosmetic Uses of Oxalaldehyde: antimicrobial agents
Coated paper and textile finishes use large amounts of Oxalaldehyde as a crosslinker for starch-based formulations.
Oxalaldehyde is used as a solubilizer and cross-linking agent in polymer chemistry.
Oxalaldehyde solutions can also be used as a fixative for histology, that is, a method of preserving cells for examining them under a microscope.


Oxalaldehyde is mainly used in the textile industry, and the fiber treatment agent can increase the spinning and anti-wrinkle properties of cotton, nylon and other fibers, and is a durability pressing finishing agent.
In Japan, this use accounts for 80% of the total consumption of Oxalaldehyde.
Oxalaldehyde is an insoluble adhesive such as gelatin, animal glue, cheese, polyvinyl alcohol and starch.


Oxalaldehyde is also used in the leather industry and in making waterproof matches.
Hydroxyphenylacetic acid produced by Oxalaldehyde has been industrially produced in Japan and used as an intermediate for antimicrobials and vitamin A series of products.
Oxalaldehyde is also used for the synthesis of berberine hydrochloride and sulfonamide.


Oxalaldehyde is also used in insecticide remover, deodorant, body preservative, sand curing agent.
Oxalaldehyde and the ring are used to obtain benzypyrazine.
Oxalaldehyde is mainly used as raw materials for glyoxylic acid, M2D resin, imidazole and other products, as well as insoluble adhesives for gelatin, animal glue, cheese, polyvinyl alcohol and starch, and shrinkage inhibitors for rayon.


In medicine, Oxalaldehyde is mainly used for special cycloimidazole drugs, such as metronidazole, dimethylnitroimidazole, imidazole, etc.
In terms of intermediates, Oxalaldehyde is mainly used as glyoxylic acid, D-p-hydroxyphenylglycine, allantoin, phenylpharyngeal enzyme, berberine, etc.
In light textile, Oxalaldehyde is mainly used as garment finishing agent, 2D resin, M2D resin, etc.


In the paper industry, Oxalaldehyde is mainly used as sizing agent to increase the moisture resistance of paper.
Oxalaldehyde is a very effective crosslinking factor in polymer chemistry and can be used as crosslinking agent.
In the construction industry, Oxalaldehyde can be used as the curing agent of cement to improve the setting strength and control landslides, which can prevent soil loss and collapse.


Oxalaldehyde is used as a solubilizer and cross-linking agent in polymer chemistry for: proteins (leather tanning process), collagen, cellulose derivatives (textiles), hydrocolloids, and starch (paper coatings).
Coated paper and textile finishes use large amounts of Oxalaldehyde as a crosslinker for starch-based formulations.
Oxalaldehyde condenses with urea to afford 4,5-dihydroxy-2-imidazolidinone, which further reacts with formaldehyde to give the bis(hydroxymethyl) derivative used for wrinkle-resistant chemical treatments.


Oxalaldehyde, 40 % Solution is used to denature nucleic acids by forming stable complexes with guanine residues
Oxalaldehyde is used Manufacture of organic products, manufacture of resins.
Oxalaldehyde can be found in garden tomato (variety), ginger, and sesame, which makes Oxalaldehyde a potential biomarker for the consumption of these food products.


Oxalaldehyde is a versatile crosslinking agent used in a variety of applications including textiles, paper, epoxy curing, cosmetics, oil & gas, and cleaners.
Oxalaldehyde 40% is most widely used as a cross-linking agent for the resins for textiles, leathers and papers, for water soluble polymers such as carboxy methyl cellulose and cellulose ethers, for H2S scavenger in oil & gas fields.
Oxalaldehyde is also used as intermediate for pharmaceuticals and pesticides.


Oxalaldehyde is used in paper and textile production, leather tanning, textile dyeing, embalming, curing and cross-linking polymers.
Oxalaldehyde is also used as biocide and disinfectant and to make proteins and other materials insoluble.
Oxalaldehyde is used in organic synthesis and glues.
Oxalaldehyde is used predominantly as a chemical intermediate.


Oxalaldehyde is also used as reducing agent in the photographic industry and to make silvered mirrors;
Oxalaldehyde, difunctional low mole weight aldehyde, is a highly reactive intermediate used for the preparation of copolymers, dyes, pharmaceuticals, pesticides, corrosion inhibitors and photographic chemicals.
Oxalaldehyde is used as a dispersant water soluble polymers, starches, cellulosic materials, proteins (casein, gelatin and animal glue), and polyhydroxyl groups.


Oxalaldehyde is used in soil and cement stabilizing.
Oxalaldehyde is also used to improve moisture resistance in paper, leather and glue.
Oxalaldehyde is used in embalming fluids, for leather tanning, and for rayon shrink-proofing.
Oxalaldehyde is used as a sulfide scavenger.


Oxalaldehyde is used permanent-press fabrics; dimensional stabilization of rayon and other fibers. Insolubilizing agent for compounds containing polyhydroxyl groups (polyvinyl alcohol, starch, and cellulosic materials); insolubilizing of proteins (casein, gelatin, and animal glue); embalming fluids; leather tanning; paper coatings with hydroxyethylcellulose; reducing agent in dyeing textiles.
Oxalaldehyde is used in the production of textilesand glues and in organic synthesis.
Oxalaldehyde is used to prepare 4,5-dihydroxy-2-imidazolidinone by condensation with urea.


Oxalaldehyde finds application in leather tanning process, textile finishes and paper coatings.
Oxalaldehyde is an important building block in the synthesis of imidazoles.
Oxalaldehyde acts as a solubilizer and cross-linking agent in polymer chemistry.
Further, Oxalaldehyde is used as a fixative for histology to preserve cells in order to examine under a microscope.



PRODUCTION of OXALALDEHYDE:
Oxalaldehyde was first prepared and named by the German-British chemist Heinrich Debus (1824–1915) by reacting ethanol with nitric acid.
Commercial Oxalaldehyde is prepared either by the gas-phase oxidation of ethylene glycol in the presence of a silver or copper catalyst (the Laporte process) or by the liquid-phase oxidation of acetaldehyde with nitric acid.
Industrial synthesis of Oxalaldehyde (Laporte-process).svg
Industrial synthesis of Oxalaldehyde (acetaldehyde process).svg
The first commercial Oxalaldehyde source was in Lamotte, France, started in 1960.
The single largest commercial source is BASF in Ludwigshafen, Germany, at around 60,000 tons per year.
Other production sites exist also in the US and China.
Commercial bulk Oxalaldehyde is made and reported as a 40% solution in water by weight (approx. 1:5 molar ratio of Oxalaldehyde to water).



LABORATORY METHODS of OXALALDEHYDE:
Oxalaldehyde may be synthesized in the laboratory by oxidation of acetaldehyde with selenious acid or by ozonolysis of benzene.
Anhydrous Oxalaldehyde is prepared by heating solid Oxalaldehyde hydrate(s) with phosphorus pentoxide and condensing the vapors in a cold trap.



ALTERNATIVE PARENTS of OXALALDEHYDE:
*Organic oxides
*Hydrocarbon derivatives



SUBSTITUENTS of OXALALDEHYDE:
*Organic oxide
*Hydrocarbon derivative
*Short-chain aldehyde
*Aliphatic acyclic compound



SPECIATION IN SOLUTION of OXALALDEHYDE:
Oxalaldehyde is supplied typically as a 40% aqueous solution.
Like other small aldehydes, Oxalaldehyde forms hydrates.
Furthermore, the hydrates condense to give a series of oligomers, some of which remain of uncertain structure.
For most applications, the exact nature of the species in solution is inconsequential.
At least one hydrate of Oxalaldehyde is sold commercially, Oxalaldehyde trimer dihydrate: [(CHO)2]3(H2O)2 (CAS 4405-13-4).
Other Oxalaldehyde equivalents are available, such as the ethylene glycol hemiacetal 1,4-dioxane-trans-2,3-diol (CAS 4845-50-5, m.p. 91–95 °C).

It is estimated that, at concentrations less than 1 M, Oxalaldehyde exists predominantly as the monomer or hydrates thereof, i.e., OCHCHO, OCHCH(OH)2, or (HO)2CHCH(OH)2.
At concentrations above 1 M, dimers predominate.
These dimers are probably dioxolanes, with the formula [(HO)CH]2O2CHCHO.
Dimer and trimers precipitate as solids from cold solutions.



PHYSICAL and CHEMICAL PROPERTIES of OXALALDEHYDE:
Molecular Weight: 58.04
Chemical formula: C2H2O2
Molar mass: 58.036 g·mol−1
Melting point: 15 °C (59 °F; 288 K)
Boiling point: 51 °C (124 °F; 324 K)
Molecular Weight: 58.04
XLogP3-AA: -0.4
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 1
Exact Mass: 58.005479302
Monoisotopic Mass: 58.005479302
Topological Polar Surface Area: 34.1 Ų
Heavy Atom Count: 4
Formal Charge: 0

Complexity: 25
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Melting point (℃): 15
Boiling point: 51℃
Refractive index: 1.3826
Relative density (water =1): 1.14
Boiling point (℃): 50.5
molecular formula:C2H2O2
Molecular weight: 58.04
Solubility: soluble in ethanol, ether, soluble in water

Physical state: clear, liquid
Color: colorless
Odor: No data available
Melting point/freezing point: No data available
Initial boiling point and boiling range: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: No data available
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: No data available
Partition coefficient: n-octanol/water: No data available

Vapor pressure: No data available
Density: 1,270 g/cm3
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: Not classified as explosive.
Oxidizing properties: none
Other safety information: No data available
Min. Purity Spec: 40% w/w aq. soln, ca. 8.8mol/L
Physical Form (at 20°C): Liquid
Melting Point: -14°C
Boiling Point: 104°C
Density: 1.27
Refractive Index: 1.41
Long-Term Storage: Store long-term in a cool, dry place

Density: 1.270 g/mL
Molar volume: 45.7 mL/mol
Refractive index: 1.383
Molecular refractive power: 10.65 mL/mol
Dipole moment: 4.80 D
Melting point: 15 °C
Boiling point: 51 °C
Water Solubility: 218 g/L
logP: -0.04
logP: -0.0036
logS: 0.57
pKa (Strongest Basic): -7.8
Physiological Charge: 0
Hydrogen Acceptor Count: 2
Hydrogen Donor Count: 0

Polar Surface Area: 34.14 Ų
Rotatable Bond Count: 1
Refractivity: 12.56 m³·mol⁻¹
Polarizability: 4.5 ų
Number of Rings: 0
Bioavailability: Yes
Rule of Five: Yes
Ghose Filter: No
Veber's Rule: Yes
MDDR-like Rule: No
Appearance: colorless to pale yellow clear liquid to solid (est)
Assay: 96.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity: 1.26500 @ 25.00 °C.
Melting Point: 14.00 to 16.00 °C. @ 760.00 mm Hg
Boiling Point: 49.00 to 51.00 °C. @ 760.00 mm Hg
Vapor Pressure: 255.000000 mmHg @ 25.00 °C. (est)

Flash Point: 24.00 °F. TCC ( -4.30 °C. ) (est)
logP (o/w): -0.549 (est)
Shelf Life: 12.00 month(s) or longer if stored properly.
Storage: refrigerate in tightly sealed containers.
Melting point: -14 °C
Boiling point: 104 °C
Density: 1.265 g/mL at 25 °C
vapor density: >1 (vs air)
vapor pressure: 18 mm Hg ( 20 °C)
refractive index: n20/D 1.409
Flash point: 104°C
storage temp.: 2-8°C
solubility: water: soluble(lit.)
form: Liquid
color: Clear colorless to yellow
Water Solubility: miscible



FIRST AID MEASURES of OXALALDEHYDE:
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
Immediately call in physician.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Consult a physician.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of OXALALDEHYDE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Take up with liquid-absorbent material.
Dispose of properly.



FIRE FIGHTING MEASURES of OXALALDEHYDE:
-Extinguishing media:
Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of OXALALDEHYDE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use Safety glasses
*Skin protection:
Handle with gloves.
Wash and dry hands.
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
protective clothing
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of OXALALDEHYDE:
-Precautions for safe handling:
*Hygiene measures:
Immediately change contaminated clothing.
Wash hands and face after working with substance.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
*Storage class:
Storage class (TRGS 510): 12: Non Combustible Liquids



STABILITY and REACTIVITY of OXALALDEHYDE:
-Reactivity:
No data available
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
no information available



SYNONYMS:
GLYOXAL
Ethanedial
107-22-2
Oxalaldehyde
oxaldehyde
1,2-Ethanedione
Biformyl
Diformyl
Glyoxylaldehyde
Biformal
Diformal
Oxal
Aerotex glyoxal 40
Glyoxal aldehyde
Ethanedial, trimer
Ethanediol, trimer
Glyoxal, 40 % Solution
DTXSID5025364
CHEBI:34779
Glyoxal, 40% solution in water
50NP6JJ975
NCGC00091228-01
DSSTox_CID_5364
DSSTox_RID_77764
DSSTox_GSID_25364
Glyoxal, 40%
Ethanedione
Glyoxal solutions
CAS-107-22-2
CCRIS 952
Ethane-1,2-dione
ODIX
C2H2O2
HSDB 497
Glyoxal solution, ~40% in H2O (~8.8 M)
Glyoxal, 29.2%
EINECS 203-474-9
BRN 1732463
hydroxyketene
Ethandial
Glycoxal
ethane dial
UNII-50NP6JJ975
AI3-24108
(oxo)acetaldehyde
ethane-1,2-dial
Protectol GL 40
glyoxal (ethanedial)
MFCD00006957
oxalic acid dihydride
hydroxymethylene ketone
NSC 262684
EC 203-474-9
Glyoxal solution, 40.0%
4-01-00-03625
BIDD:ER0284
(CHO)2
Glyoxal, Biformyl, Oxalaldehyde
CHEMBL1606435
Glyoxal, 40% w/w aq. soln.
STR01281
ZINC8437750
Tox21_111105
Tox21_202517
BBL011519
NSC262684
STL146635
AKOS000119169
Glyoxal solution, 40 wt. % in H2O
NSC-262684
NCGC00260066-01
Glyoxal solution, CP, 40 wt. % in H2O
FT-0626792
G0152
Q413465
J-001740
F2191-0152
Glyoxal solution, ~40% in H2O, for HPLC derivatization
Glyoxal solution, BioReagent, for molecular biology, ~40% in H2O (~8.8 M)
Glyoxal 40%
Ethanedial
Bisformyl
Glyoxylaldehyde
Glyoxal Solution
Diformyl; Ethanedial
1,2-ethanedione
Oxalaldehyde
Unox G40
BISFORMYL
glyoxylaldehyde;GLYOXAL SOLUTION
GLYOXAL
DIFORMYL
ETHANEDIAL
1,2-ethanedione
Oxalaldehyde
1,2-Ethanedione
Aurarez 136
Biformal
Biformyl
Cartabond GH
Cartabond GHF
Daicel GY 60
Diformyl
Earth Works Linkup Plus
Ethanedione; Freechem 40DL
GX
GX (aldehyde)
Glyfix CS 50
Glyoxal 40L
Glyoxal T 40
Glyoxal aldehyde
Glyoxazal
Glyoxazal GX Glyoxylaldehyde
Gohsezal P
Oxal
Oxalaldehyde
Permafresh 114
Protorez BLF-C
XH 536
1,2-Ethanedione
BIFORMAL
BIFORMYL
DIFORMAL
DIFORMYL
ETHANDIAL
ETHANEDIAL
ETHANEDIONE
Ethanedione-1,2
Glyoxal
GLYOXAL ALDEHYDE
Glyoxal
GLYOXYLALDEHYDE
OXAL
OXALALDEHYDE
OXALIC ALDEHYDE
(CHO)2 biospider
1,2-Ethanedione
Aerotex glyoxal 40
Biformal
Biformyl
Diformal
Diformyl
Ethandial
Ethane-1,2-dial
Ethane-1,2-dione
1,2-Ethanedione
Aerotex glyoxal 40
Biformal
Biformyl
Diformal
Diformyl
Ethanedial
Glyoxylaldehyde
Oxal
Oxalaldehyde
Glyoxal, 29.2%
Glyoxal, 40%
Glyoxal solutions
Glyoxal Solution
1,2-Ethanedione
Aurarez 136
Biformal; Biformyl
Cartabond GH
Cartabond GHF
Daicel GY 60
Diformyl
Earth Works Linkup Plus
Ethanedione
Freechem 40DL
GX
GX (aldehyde)
Glyfix CS 50
Glyoxal 40L
Glyoxal T 40
Glyoxal aldehyde
Glyoxazal
Glyoxazal GX
Glyoxylaldehyde
Gohsezal P
Oxal
Oxalaldehyde
Permafresh 114
Protorez BLF-C
Oxalaldehyde
Oxaldehyde
GLYOXA
ETHANEDIAL
GLYOXAL SOLUTION
(CHO)2
Ethandial
DIFORMYL
Ethanedione
Glyoxal aqueous solution
OXALIC ACID
OXALIC ACID Oxalic acid (OXALIC ACID, oksalik asit) is an organic compound with the formula C2H2O4. Oxalic acid (OXALIC ACID, oksalik asit) is a white crystalline solid that forms a colorless solution in water. Its condensed formula is HOOCCOOH, reflecting its classification as the simplest dicarboxylic acid. Its acid strength is much greater than that of acetic acid. Oxalic acid (OXALIC ACID, oksalik asit) is a reducing agent and its conjugate base, known as oxalate (C2O2−4), is a chelating agent for metal cations. Typically, Oxalic acid (OXALIC ACID, oksalik asit) occurs as the dihydrate with the formula C2H2O4·2H2O. It occurs naturally in many foods, but excessive ingestion of Oxalic acid (OXALIC ACID, oksalik asit) or prolonged skin contact can be dangerous. Its name comes from the fact that early investigators isolated Oxalic acid (OXALIC ACID, oksalik asit) from flowering plants of the genus Oxalis, commonly known as wood-sorrels. History of Oxalic acid (OXALIC ACID, oksalik asit) The preparation of salts of Oxalic acid (OXALIC ACID, oksalik asit) (crab acid) from plants had been known, at the latest, since 1745, when the Dutch botanist and physician Herman Boerhaave isolated a salt from sorrel. By 1773, François Pierre Savary of Fribourg, Switzerland had isolated Oxalic acid (OXALIC ACID, oksalik asit) from its salt in sorrel. In 1776, Swedish chemists Carl Wilhelm Scheele and Torbern Olof Bergman produced Oxalic acid (OXALIC ACID, oksalik asit) by reacting sugar with concentrated nitric acid; Scheele called the acid that resulted socker-syra or såcker-syra (sugar acid). By 1784, Scheele had shown that "sugar acid" and Oxalic acid (OXALIC ACID, oksalik asit) from natural sources were identical. In 1824, the German chemist Friedrich Wöhler obtained Oxalic acid (OXALIC ACID, oksalik asit) by reacting cyanogen with ammonia in aqueous solution. This experiment may represent the first synthesis of a natural product. Preparation of Oxalic acid (OXALIC ACID, oksalik asit) Oxalic acid (OXALIC ACID, oksalik asit) (Crab Acid) is mainly manufactured by the oxidation of carbohydrates or glucose using nitric acid or air in the presence of vanadium pentoxide. A variety of precursors can be used including glycolic acid and ethylene glycol. A newer method entails oxidative carbonylation of alcohols to give the diesters of Oxalic acid (OXALIC ACID, oksalik asit): 4 ROH + 4 CO + O2 → 2 (CO2R)2 + 2 H2O These diesters are subsequently hydrolyzed to Oxalic acid (OXALIC ACID, oksalik asit). Approximately 120,000 tonnes are produced annually. Historically Oxalic acid (OXALIC ACID, oksalik asit) was obtained exclusively by using caustics, such as sodium or potassium hydroxide, on sawdust.[15] Pyrolysis of sodium formate (ultimately prepared from carbon monoxide), leads to the formation of sodium oxalate, easily converted to Oxalic acid (OXALIC ACID, oksalik asit). Laboratory methods Although it can be readily purchased, Oxalic acid (OXALIC ACID, oksalik asit) can be prepared in the laboratory by oxidizing sucrose using nitric acid in the presence of a small amount of vanadium pentoxide as a catalyst. The hydrated solid can be dehydrated with heat or by azeotropic distillation. Developed in the Netherlands, an electrocatalysis by a copper complex helps reduce carbon dioxide to Oxalic acid (OXALIC ACID, oksalik asit);[18] this conversion uses carbon dioxide as a feedstock to generate Oxalic acid (OXALIC ACID, oksalik asit). Structure of Oxalic acid (OXALIC ACID, oksalik asit) Anhydrous Oxalic acid (OXALIC ACID, oksalik asit) exists as two polymorphs; in one the hydrogen-bonding results in a chain-like structure whereas the hydrogen bonding pattern in the other form defines a sheet-like structure. Because the anhydrous material is both acidic and hydrophilic (water seeking), it is used in esterifications. Reactions of Oxalic acid (OXALIC ACID, oksalik asit) Oxalic acid (OXALIC ACID, oksalik asit) is a relatively strong acid, despite being a carboxylic acid: C2O4H2 ⇌ C2O4H− + H+ pKa = 1.27 C2O4H− ⇌ C2O2−4 + H+ pKa = 4.27 Oxalic acid (OXALIC ACID, oksalik asit) undergoes many of the reactions characteristic of other carboxylic acids. It forms esters such as dimethyl oxalate (m.p. 52.5 to 53.5 °C (126.5 to 128.3 °F)). It forms an acid chloride called oxalyl chloride. Oxalate, the conjugate base of Oxalic acid (OXALIC ACID, oksalik asit), is an excellent ligand for metal ions, e.g. the drug oxaliplatin. Oxalic acid (OXALIC ACID, oksalik asit) and oxalates can be oxidized by permanganate in an autocatalytic reaction. Oxalic acid (OXALIC ACID, oksalik asit)'s pKa values vary in the literature from 1.25-1.46 and 3.81-4.40. The 100th ed of the CRC, released in 2019 has values of 1.25 and 3.81. Occurrence of Oxalic acid (OXALIC ACID, oksalik asit) Biosynthesis At least two pathways exist for the enzyme-mediated formation of oxalate. In one pathway, oxaloacetate, a component of the Krebs citric acid cycle, is hydrolyzed to oxalate and acetic acid by the enzyme oxaloacetase: [O2CC(O)CH2CO2]2− + H2O → C2O2−4 + CH3CO−2 + H+ It also arises from the dehydrogenation of glycolic acid, which is produced by the metabolism of ethylene glycol. Occurrence in foods and plants Calcium oxalate is the most common component of kidney stones. Early investigators isolated Oxalic acid (OXALIC ACID, oksalik asit) from wood-sorrel (Oxalis). Members of the spinach family and the brassicas (cabbage, broccoli, brussels sprouts) are high in oxalates, as are sorrel and umbellifers like parsley.[27] Rhubarb leaves contain about 0.5% Oxalic acid (OXALIC ACID, oksalik asit), and jack-in-the-pulpit (Arisaema triphyllum) contains calcium oxalate crystals. Similarly, the Virginia creeper, a common decorative vine, produces Oxalic acid (OXALIC ACID, oksalik asit) in its berries as well as oxalate crystals in the sap, in the form of raphides. Bacteria produce oxalates from oxidation of carbohydrates. Plants of the genus Fenestraria produce optical fibers made from crystalline Oxalic acid (OXALIC ACID, oksalik asit) to transmit light to subterranean photosynthetic sites.[28] Carambola, also known as starfruit, also contains Oxalic acid (OXALIC ACID, oksalik asit) along with caramboxin. Citrus juice contains small amounts of Oxalic acid (OXALIC ACID, oksalik asit). Citrus fruits produced in organic agriculture contain less Oxalic acid (OXALIC ACID, oksalik asit) than those produced in conventional agriculture. The formation of naturally occurring calcium oxalate patinas on certain limestone and marble statues and monuments has been proposed to be caused by the chemical reaction of the carbonate stone with Oxalic acid (OXALIC ACID, oksalik asit) secreted by lichen or other microorganisms. Production by fungi Many soil fungus species secrete Oxalic acid (OXALIC ACID, oksalik asit), resulting in greater solubility of metal cations, increased availability of certain soil nutrients, and can lead to the formation of calcium oxalate crystals. Other Oxidized bitumen or bitumen exposed to gamma rays also contains Oxalic acid (OXALIC ACID, oksalik asit) among its degradation products. Oxalic acid (OXALIC ACID, oksalik asit) may increase the leaching of radionuclides conditioned in bitumen for radioactive waste disposal. Biochemistry The conjugate base of Oxalic acid (OXALIC ACID, oksalik asit) is the hydrogenoxalate anion, and its conjugate base (oxalate) is a competitive inhibitor of the lactate dehydrogenase (LDH) enzyme. LDH catalyses the conversion of pyruvate to lactic acid (end product of the fermentation (anaerobic) process) oxidising the coenzyme NADH to NAD+ and H+ concurrently. Restoring NAD+ levels is essential to the continuation of anaerobic energy metabolism through glycolysis. As cancer cells preferentially use anaerobic metabolism (see Warburg effect) inhibition of LDH has been shown to inhibit tumor formation and growth, thus is an interesting potential course of cancer treatment. Applications About 25% of produced Oxalic acid (OXALIC ACID, oksalik asit) will be used as a mordant in dyeing processes. Oxalic acid (OXALIC ACID, oksalik asit) is used in bleaches, especially for pulpwood. Oxalic acid (OXALIC ACID, oksalik asit) is also used in baking powder and as a third reagent in silica analysis instruments. Cleaning of Oxalic acid (OXALIC ACID, oksalik asit) Oxalic acid (OXALIC ACID, oksalik asit)'s main applications include cleaning or bleaching, especially for the removal of rust (iron complexing agent). Its utility in rust removal agents is due to its forming a stable, water-soluble salt with ferric iron, ferrioxalate ion. Extractive metallurgy Oxalic acid (OXALIC ACID, oksalik asit) is an important reagent in lanthanide chemistry. Hydrated lanthanide oxalates form readily in very strongly acidic solutions in a densely crystalline, easily filtered form, largely free of contamination by nonlanthanide elements. Thermal decomposition of these oxalates gives the oxides, which is the most commonly marketed form of these elements. Oxalic acid (OXALIC ACID, oksalik asit) is used by some beekeepers as a miticide against the parasitic varroa mite. Oxalic acid (OXALIC ACID, oksalik asit) is used to clean minerals. Oxalic acid (OXALIC ACID, oksalik asit) is sometimes used in the aluminum anodizing process, with or without sulfuric acid. Compared to sulfuric acid anodizing, the coatings obtained are thinner and exhibit lower surface roughness. Oxalic acid (OXALIC ACID, oksalik asit) is an ingredient in some tooth whitening products. Toxicity of Oxalic acid (OXALIC ACID, oksalik asit) Oxalic acid (OXALIC ACID, oksalik asit) in concentrated form can have harmful effects through contact and if ingested. It is not identified as mutagenic or carcinogenic, although there is a study suggesting it might cause breast cancer; there is a possible risk of congenital malformation in the fetus; may be harmful if inhaled, and is extremely destructive to tissue of mucous membranes and upper respiratory tract; harmful if swallowed; harmful to and destructive of tissue and causes burns if absorbed through the skin or is in contact with the eyes. Symptoms and effects include a burning sensation, cough, wheezing, laryngitis, shortness of breath, spasm, inflammation and edema of the larynx, inflammation and edema of the bronchi, pneumonitis, pulmonary edema. In humans, ingested Oxalic acid (OXALIC ACID, oksalik asit) has an oral LDLo (lowest published lethal dose) of 600 mg/kg. It has been reported that the lethal oral dose is 15 to 30 grams. Oxalate may enter cells where it is known to cause mitochondrial dysfunction. The toxicity of Oxalic acid (OXALIC ACID, oksalik asit) is due to kidney failure caused by precipitation of solid calcium oxalate, the main component of calcium kidney stones. Oxalic acid (OXALIC ACID, oksalik asit) can also cause joint pain by formation of similar precipitates in the joints. Ingestion of ethylene glycol results in Oxalic acid (OXALIC ACID, oksalik asit) as a metabolite which can also cause acute kidney failure. Oxalic acid (OXALIC ACID, oksalik asit) is an odorless white solid. Sinks and mixes with water. Oxalic acid (OXALIC ACID, oksalik asit) is an alpha,omega-dicarboxylic acid that is ethane substituted by carboxyl groups at positions 1 and 2. Oxalic acid (OXALIC ACID, oksalik asit) has a role as a human metabolite, a plant metabolite and an algal metabolite. It is a conjugate acid of an oxalate(1-) and an oxalate. The absorption of (14)C-labelled Oxalic acid (OXALIC ACID, oksalik asit) was studied in Wistar rats, CD-1 mice and NMRI mice. Oxalic acid (OXALIC ACID, oksalik asit) in solution was given to the animals by gavage either with water alone or with 0.625 g/kg body wt of xylitol. Both xylitol adapted animals and animals not previously exposed to xylitol were used. Adaptation to xylitol diets enhanced the absorption and urinary excretion of the label (Oxalic acid (OXALIC ACID, oksalik asit)) in both strains of mice but not in rats. Earlier studies have indicated a high incidence of bladder calculi in mice but not in rats fed high amounts of xylitol. The results of the present study offer one likely explanation for the increased formation of bladder calculi as a result of over saturation of urine with oxalate. Piridoxilate is an association of glyoxylic acid and pyridoxine in which pyridoxine is supposed to facilitate in vivo transformation of glyoxylic acid to glycine rather than to Oxalic acid (OXALIC ACID, oksalik asit). However, it has recently been shown that long term treatment with piridoxilate may result in over production of Oxalic acid (OXALIC ACID, oksalik asit) and in calcium oxalate nephrolithiasis. A patient in whom piridoxilate induced both oxalate nephrolithiasis and chronic oxalate nephropathy with renal insufficiency, an association that has not been previously described, was reported. Therefore, piridoxilate should be added to the list of chemicals responsible for chronic oxalate nephropathy. Metabolically its toxicity is believed due to the capacity of Oxalic acid (OXALIC ACID, oksalik asit) to immobilize calcium and thus upset the calcium-potassium ratio in critical tissues. Oxalic acid (OXALIC ACID, oksalik asit) is a waste chemical stream constituent which may be subjected to ultimate disposal by controlled incineration. Pretreatment involves chemical reaction with limestone or calcium oxide forming calcium oxalate. This may then be incinerated utilizing particulate collection equipment to collect calcium oxide for recycling. Residues of Oxalic acid (OXALIC ACID, oksalik asit) are exempted from the requirement of a tolerance when used as a calcium chelating hard water inhibitor in accordance with good agricultural practices as inert (or occasionally active) ingredients in pesticide formulations applied to growing crops or to raw agricultural commodities after harvest. Limits: No more Oxalic acid (OXALIC ACID, oksalik asit) should be used than is necessary to chelate calcium and, in no case, should more than 2 lb Oxalic acid (OXALIC ACID, oksalik asit) per acre be used. Oxalic acid (OXALIC ACID, oksalik asit) is hygroscopic and sensitive to heat. This compound may react violently with furfuryl alcohol, silver, sodium, perchlorate, sodium hypochlorite, strong oxidizers, sodium chlorite, acid chlorides, metals and alkali metals. (NTP, 1992). The heating of mixtures of Oxalic acid (OXALIC ACID, oksalik asit) and urea has lead to explosions. This is due to the rapid generation of the gases CO2, CO, and NH3. Oxalic acid (OXALIC ACID, oksalik asit) and urea react at high temperatures to form toxic and flammable ammonia and carbon monoxide gases, and inert CO2 gas Residues of Oxalic acid (OXALIC ACID, oksalik asit) are exempted from the requirement of a tolerance when used as a calcium chelating hard water inhibitor in accordance with good agricultural practices as inert (or occasionally active) ingredients in pesticide formulations applied to growing crops or to raw agricultural commodities after harvest. Limits: No more Oxalic acid (OXALIC ACID, oksalik asit) should be used than is necessary to chelate calcium and, in no case, should more than 2 lb Oxalic acid (OXALIC ACID, oksalik asit) per acre be used. Oxalic acid (OXALIC ACID, oksalik asit) is naturally contained as the potassium or calcium salt in plants, vegetables, human urine, animal urine, and kidney stones. It is also the product of the metabolism of many molds. Oxalic acid (OXALIC ACID, oksalik asit) may be released to the environment in tobacco smoke, automobile exhaust, rendering, in waste streams from pulp bleaching, and by photochemical oxidations of anthropogenic compounds during long range transport. If released to soil, Oxalic acid (OXALIC ACID, oksalik asit) under environmental conditions (pH 5-9) will be in the form of the oxalate ion (pKa1 and pKa2 of 1.25 and 4.28, respectively) and is expected to leach in soil. Photolysis is expected to be an important fate process; the daytime persistence of Oxalic acid (OXALIC ACID, oksalik asit) on soil surfaces is not expected to exceed a few hours. Based upon screening biodegradation tests, biodegradation in soil is expected to be important. If released to water, Oxalic acid (OXALIC ACID, oksalik asit) will not volatilize, adsorb to sediment, bioconcentrate in aquatic organisms, oxidize or hydrolyze. The predominant aquatic fate processes are expected to be photolysis in surface waters and aerobic and anaerobic biodegradation. If released to the atmosphere, removal from air via wet deposition, dry deposition, and photolysis is likely to occur. Exposure of the general population to Oxalic acid (OXALIC ACID, oksalik asit) is expected to occur through consumption of foods in which it is naturally contained, inhalation of contaminated air, and consumption of contaminated groundwater. In occupational settings, exposure to Oxalic acid (OXALIC ACID, oksalik asit) may occur through inhalation of vapors and through eye and skin contact. Oxalic acid (OXALIC ACID, oksalik asit) may be released to the environment as emissions from rendering, tobacco smoke(1), and automobile exhaust(2). Oxalic acid (OXALIC ACID, oksalik asit) may be produced in the atmosphere by photochemical oxidations of anthropogenic compounds during long range transport(3). Oxalic acid (OXALIC ACID, oksalik asit) has been identified in pulp kraft mill effluents(4-6); therefore, it may be released to the environment in waste streams resulting from pulp bleaching(SRC). The estimated emission rate of Oxalic acid (OXALIC ACID, oksalik asit) in the South East Air Basin, CA is 87 kg/day(7). TERRESTRIAL FATE: An estimated Koc value of 5(1,SRC) for Oxalic acid (OXALIC ACID, oksalik asit) indicates high mobility in soil(2) and Oxalic acid (OXALIC ACID, oksalik asit) has been detected in groundwater(3). Volatilization from moist soils is not expected to be rapid based upon a low Henry's Law constant. Several screening studies indicate rapid biodegradation of Oxalic acid (OXALIC ACID, oksalik asit)(4-8). Although these studies are not specific to soil media, they suggest that Oxalic acid (OXALIC ACID, oksalik asit) will readily biodegrade in soil. The Oxalic acid (OXALIC ACID, oksalik asit) concn in another study was determined to decrease from 30 mg/kg on a soil surface to about 6 mg/kg 540 cm below the soil surface(3) which suggests that biodegradation may have occurred(SRC). Photolysis is expected to be an important terrestrial fate process; the daytime persistence of Oxalic acid (OXALIC ACID, oksalik asit) on soil surfaces is not expected to exceed a few hours(9). AQUATIC FATE: Several screening studies(4-8) and grab sample tests(9) indicate that under aerobic and anaerobic conditions, Oxalic acid (OXALIC ACID, oksalik asit) will readily biodegrade in aquatic ecosystems. Based on an experimental Henry's Law constant of 1.4X10-10 atm-cu m/mole at 25 °C(2), Oxalic acid (OXALIC ACID, oksalik asit) is expected to be essentially nonvolatile from water(1). Adsorption to sediment and bioconcentration in aquatic organisms may not be important fate processes for Oxalic acid (OXALIC ACID, oksalik asit) in water systems. Based on pKa1 and pKa2 values of 1.25 and 4.28(3), respectively, Oxalic acid (OXALIC ACID, oksalik asit) will exist primarily as the oxalate ion under environmental conditions (pH 5-9,SRC). Aquatic oxidation is not likely to be an important fate process based on a half-life of 285 yrs in water under continuous sunlight(3,SRC). Oxalic acid (OXALIC ACID, oksalik asit) may react slowly in water with photochemically produced OH radicals, but it is expected to be removed rapidly from surface water by direct photolysis; the daytime persistence of Oxalic acid (OXALIC ACID, oksalik asit) is not expected to exceed a few hours(10). ATMOSPHERIC FATE: Based on a measured vapor pressure of 2.3410-4 mm Hg at 25 °C(2), Oxalic acid (OXALIC ACID, oksalik asit) is expected to exist almost entirely in the vapor phase in the ambient atmosphere(3). In the vapor phase, Oxalic acid (OXALIC ACID, oksalik asit) in the ambient atmosphere is very slowly degraded by reaction with photochemically formed hydroxyl radicals; the half-life for this reaction in air can be estimated to be about 223 days(1). Oxalic acid (OXALIC ACID, oksalik asit) in the ambient atmosphere may react slowly with OH radicals, but it is removed rapidly by photolysis; the daytime persistence of Oxalic acid (OXALIC ACID, oksalik asit) is not expected to exceed a few hours(4). Based on its high water solubility, removal from air via wet deposition is likely to occur(4,SRC). Oxalic acid (OXALIC ACID, oksalik asit) may also be removed from air via dry deposition with 11% of the total deposition being dry deposition(4). Six tests at Oxalic acid (OXALIC ACID, oksalik asit) initial concns of 3.3 to 10 ppm exhibited 75 to 202 %BODT over an incubation period of 5 days in an aerobic screening study using sewage inoculum(1). A 78 and 55.5 %BODT for Oxalic acid (OXALIC ACID, oksalik asit) was measured under aerobic conditions over a period of 5 days in screening tests at 20 °C using sewage inoculum(2). Oxalic acid (OXALIC ACID, oksalik asit) at initial concns of 0.00375, 0.0375, and 0.375 ppm exhibited 95, 99, and 100% degradation, respectively, in an aerobic screening study at 25 °C using sewage inoculum(3). In another screening study using sewage inoculum, 68 and 64 %BODT were measured for Oxalic acid (OXALIC ACID, oksalik asit) at initial concns of 10 and 20 ppm, respectively, over a 5 day incubation period(4). An 89 %BODT was measured for Oxalic acid (OXALIC ACID, oksalik asit) (10 ppm initial concn) in an aerobic screening study using sewage inoculum at 19.5-20.5 °C over an incubation period of 5 days(5). The rate constant for the vapor-phase reaction of Oxalic acid (OXALIC ACID, oksalik asit) with photochemically produced hydroxyl radicals can be estimated to be 7.2X10-14 cu cm/molecule-sec at 25 °C which corresponds to an atmospheric half-life of about 223 days at an atmospheric concn of 5X10+5 hydroxyl radicals per cu cm(1,SRC). Acids are generally resistent to hydrolysis(4); therefore, Oxalic acid (OXALIC ACID, oksalik asit) is not expected to hydrolyze in aquatic environments. Based on dissociation constant values pKa1 and pKa2 of 1.25 and 4.28(1), respectively; Oxalic acid (OXALIC ACID, oksalik asit) is expected to exist as an ion under environmental conditions (pH 5-9). The aquatic oxidation rate for the reaction of hydroxyl radicals in water with the oxalate ion has been experimentally determined to be 7.7X10+6 L/mole-s at pH 6(1). Based on this rate and a hydroxyl radical concn of 1X10-17 mole/L in water under continuous sunlight(3), the half-life for the aquatic oxidation of Oxalic acid (OXALIC ACID, oksalik asit) can be estimated to be 285 yrs(SRC). Oxalic acid (OXALIC ACID, oksalik asit) may react slowly with OH in water, but it is removed rapidly by direct photolysis; the daytime persistence of Oxalic acid (OXALIC ACID, oksalik asit) is not expected to exceed a few hours(5). Based on an average experimental water solubility of 220,000 mg/L at 25 °C(1) and a regression derived equation(2), the Koc for undissociated Oxalic acid (OXALIC ACID, oksalik asit) can be estimated to be approximately 5. This Koc value indicates that Oxalic acid (OXALIC ACID, oksalik asit) will have very high mobility in soil(3); therefore, adsorption to soil and sediment may not be an important fate process. Based on pKa1 and pKa2 values of 1.25 and 4.28(4) respectively, Oxalic acid (OXALIC ACID, oksalik asit) will exist primarily as the oxalate ion under environmental conditions (pH 5-9). No experimental data are available to determine whether the oxalate ion will adsorb to sediment or soil more strongly than its estimated Koc value indicates(SRC).
OXALIC ACID
Oxalic acid is a dicarboxylic acid with a chemical formula C2H2O4.
Oxalic acid is also known as Ethanedioic acid or Oxiric acid.
Oxalic acid is found in many vegetables and plants.
Oxalic acid is the simplest dicarboxylic acid with condensed formula HOOC-COOH and has an acidic strength greater than acetic acid.


CAS Number: 144-62-7 (anhydrous)
6153-56-6 (dihydrate)
EC Number: 205-634-3
MDL number: MFCD00002573
Molecular Formula: C2H2O4 or (COOH)2 or HOOCCOOH


Oxalic acid is an odorless white solid.
Oxalic acid sinks and mixes with water.
Oxalic acid is a reducing agent and Oxalic acid's conjugate base, known as oxalate (C2O2−4), is a chelating agent for metal cations.


Typically, Oxalic acid occurs as the dihydrate with the formula C2H2O4•2H2O.
Oxalic acid is an alpha,omega-dicarboxylic acid that is ethane substituted by carboxyl groups at positions 1 and 2.
The body also produces Oxalic acid as waste.


Foods rich in oxalates also contain other nutrients that your body needs for good health.
Oxalic acid has a role as a human metabolite, a plant metabolite and an algal metabolite.
Oxalic acid is manufactured by heating sodium formate in the presence of an alkali catalyst, by oxidizing carbohydrates with nitric acid, by heating sawdust with caustic alkalies, or by fermentation of sugar solutions in the presence of certain molds.


Oxalic acid is a conjugate acid of an oxalate(1-) and an oxalate.
Oxalic acid is a metabolite found in or produced by Escherichia coli.
Oxalic acid is the simplest dicarboxylic acid and has two hydrogen atoms, two carbon atoms, and four oxygen atoms.


Oxalic acid, also called ethanedioic acid, a colourless, crystalline, toxic organic compound belonging to the family of carboxylic acids.
Oxalic acid is a colorless crystalline solid that dissolves in water to give colorless solutions.
Oxalic acid is mainly produced by the oxidation of carbohydrates or glucose in the presence of vanadium pentoxide using nitric acid or air.


Oxalic acid is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 to < 100 000 tonnes per annum.
The formula of oxalic acid is (C2H2O4); its usual form is that of the crystalline hydrate, (COOH)2·2H2O.


Oxalic acid, which is shown with the chemical formula COOH2, is found in nature as a calcium salt in the rhubarb plant, in the plant called sorrel as the sodium salt, and in the sap of some plants.
Most plant sources contain this organic acid.
Plants such as spinach, tomatoes, sorrel are in it.


The density of anhydrous Oxalic acid is 1.90 grams / cubic centimeter.
The density of Oxalic acid dihydrate is 1.653 grams per cubic centimeter.
Oxalic acid is known as a constituent of wood sorrel as early as the 17th century, oxalic acid was first prepared synthetically in 1776.


The formula of Oxalic acid is (C2H2O4); Oxalic acid's usual form is that of the crystalline hydrate, (COOH)2•2H2O.
Oxalic acid is manufactured by heating sodium formate in the presence of an alkali catalyst, by oxidizing carbohydrates with nitric acid, by heating sawdust with caustic alkalies, or by fermentation of sugar solutions in the presence of certain molds.


Oxalic acid, which enters a biologically living system and body, forms salts with ions there.
Calcium oxalate, which is the most common salt, accumulates in the body, usually in the urinary system, especially in the kidneys, causing stone formation.
Oxalic acid, also called Oxalic acid, a colourless, crystalline, toxic organic compound belonging to the family of carboxylic acids.


Oxalic acid is an organic compound found in many plants, including leafy greens, vegetables, fruits, cocoa, nuts, and seeds.
In plants, it’s usually bound to minerals, forming oxalate.
The terms “oxalic acid” and “oxalate” are used interchangeably in nutrition science.


Leafy greens, legumes, and most other plant foods contain a nutrient called oxalate or Oxalic acid.
Oxalic acid's a naturally occurring chemical you get through your diet.
In other words, the rates vary for each region.


Oxalic acid is recommended to apply this once a year.
When Oxalic acid mixes with other minerals, it forms oxalate.
People regularly use the two terms interchangeably to refer to the same thing.


Your body produces oxalate and also gets it from food sources.
The molecular weight of the dihydrate of Oxalic acid is equivalent to 126.065 grams per mole.
Under standard conditions, Oxalic acid exists as an essentially crystalline white solid and is odorless.


Your body can produce oxalate on its own or obtain it from food.
Vitamin C can also be converted into oxalate when it’s metabolized.
Once consumed, oxalate can bind to minerals to form compounds, including calcium oxalate and iron oxalate.


Oxalic acid is an organic, hydrophilic, toxic reducing agent; the simplest dicarboxylic acid.
Apart from that, Oxalic acid is also produced in the body by metabolism of ascorbic acid or glyoxylic acid.
Because Oxalic acid is an acid, Oxalic acid can form a salt with an ion in the environment.


Oxalic acid is applied by mixing some Oxalic acid into the sugar syrup prepared with warm water and dripping on the bees when the bee is in clusters and there are no closed brood at an outdoor temperature below 10 degrees.
Oxalic acid used in the control of varroa in honey bees is Oxalic acid hydrate with the chemical formula C2H2O4 - 2H2O.


Oxalic acid dihydrate has been evaluated as a treatment for reducing populations of naturally occurring microorganisms.
Oxalic acid belongs to the class of organic compounds known as dicarboxylic acids and derivatives.
Oxalic acid is one of the strongest organic acids with pKa values of 1.3 and 4.3 and is a widely occurring natural product of animals, plants and other organisms.


Oxalic acid, which is otherwise known as Oxalic acid, is a colorless, crystalline, organic compound from the dicarboxylic acid family found in many plants.
This mostly occurs in the colon, but can also take place in the kidneys and other parts of the urinary tract.
Oxalic acid is an odorless white solid.


Oxalic acid sinks and mixes with water.
Oxalic acid is also a reducing agent.
The anions of Oxalic acid as well as Oxalic acid's salts and esters are known as oxalates.


In most people, these compounds are then eliminated in the stool or urine.
Oxalic acid is an organic acid with the IUPAC name Oxalic acid and formula HO2C−CO2H.
Oxalic acid is the simplest dicarboxylic acid.


In order to make these, there are evaporation apparatuses inside the hive, and Oxalic acid is evaporated outside and sent into the hive through a pipe.
Oxalic acid is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 to < 100 000 tonnes per annum.


Oxalic acid’s molar mass of 90.03 g/mol and has two carboxylic acid (COOH) groups.
Oxalic acid is a naturally occurring organic acid in plants, vegetables, etc.
These are organic compounds containing exactly two carboxylic acid groups.


Oxalic acid is produced in the body by metabolism of glyoxylic acid or ascorbic acid.
Oxalic acid may also be synthesized via the metabolism of either glyoxylic acid or unused ascorbic acid (vitamin C), which is a serious health consideration for long term megadosers of vitamin C supplements.


Oxalic acid has a minimum purity of 98%.
Oxalic acid is an organic compound with the formula H2C2O4 also known as Oxalic acid.
Oxalic acid is the chemical compound with the formula H2C2O4.


This dicarboxylic acid, Oxalic acid, is better described with the formula HO2CCO2H.
When dissolved in water, Oxalic acid is known to form a colorless solution.
Oxalic acid is considered to be the simplest dicarboxylic acid because Oxalic acid is composed of two carboxyl groups.


Oxalic acid is produced by the oxidation of carbohydrates.
Oxalic acid is a white crystalline solid that forms a colorless solution in water.
Oxalic acid is an organic compound with the formula C2H2O4.


The molecular weight of anhydrous Oxalic acid is 90.034 grams per mole.
Oxalic acid is very soluble in water.
The solubility of Oxalic acid in water ranges from 90 to 100 grams per liter at a temperature of 20 degrees Celsius.


Oxalic acid is soluble in both ethanol and diethyl ether.
Oxalic acid can also be prepared in the laboratory by the oxidation of sucrose in the presence of nitric acid and a catalyst like vanadium pentoxide.
Oxalic acid is also known as Oxalic acid and Oxalic acid is a colorless, crystalline, toxic organic compound.


The chemical formulation of Oxalic acid is C2H2O4 belonging to the family of carboxylic acids and the Oxalic acid's condensed formula is HOOCCOOH, reflecting Oxalic acid's classification as the simplest dicarboxylic acid.
Oxalic acid has a structure with two polymorphs and it appears as a white crystalline solid which becomes a colourless solution when dissolved in water.


Oxalic acid Dihydrate is the simplest dicarboxylic acid and appears as a white solid powder.
Oxalic acid is soluble in water and becomes colorless when dissolved in water.
Various precursors can be used, including glycolic acid and ethylene glycol.


A newer method requires oxidative carbonylation of alcohols to yield Oxalic acid diesters.
4 ROH + 4 CO + 02 → 2 (CO2R) 2 + 2H20
Oxalic acid is one of the most well-known plant-derived organic acids.


Anhydrous Oxalic acid exists as two polymorphs; in one the hydrogen-bonding results in a chain-like structure whereas the hydrogen bonding pattern in the other form defines a sheet-like structure.
However the infusion beverage typically contains only low to moderate amounts of Oxalic acid per serving, due to the small mass of leaves used for brewing.


Oxalic acid is an important reagent in lanthanide chemistry.
Hydrated lanthanide oxalate forms readily in very strongly acidic solutions, in a densely crystallized, easily leached state, primarily free of contamination by non-lanthanide elements.


Thermal decomposition of this oxalate yields oxides, the most marketed form of these elements.
Oxalic acid is an organic compound.
Oxalic acid is a white crystalline solid that forms a colourless solution in water.


Many metal ions form insoluble precipitates with oxalate, a prominent example being calcium oxalate, which is the primary constituent of the most common kind of kidney stone.
Oxalic acid is colorless, odorless powder or granular solid.


Oxalic acid is a strong dicarboxylic acid occurring in many plants and vegetables.
Oxalic acid was first reported to be synthesized in 1776 and is known as a constituent of wood sorrel as early as the 17th century.
Oxalic acid is an organic acid with the systematic name ethanedioic acid and formula HO2C−CO2H.


Oxalic acid is a white crystalline solid that forms a colorless solution in water.
Oxalic acid's name comes from the fact that early investigators isolated Oxalic acid from flowering plants of the genus Oxalis, commonly known as wood-sorrels.


The chemical formula of Oxalic acid is given by C2H2O4.
Under standard temperature and pressure (STP) conditions, Oxalic acid is present as a white crystalline solid.
Oxalic acid is the simplest dicarboxylic acid.


While the amount of sugar and water in the solution remains the same, the Oxalic acid ratio may change according to the regional temperature.
Oxalic acid is a white crystalline solid that forms a colorless solution in water.
Oxalic acid's name comes from the fact that early investigators isolated oxalic acid from flowering plants of the genus Oxalis, commonly known as wood-sorrels.


Oxalic acid (IUPAC name: oxalic acid, formula H2C2O4) is a dicarboxylic acid with structure (HOOC)-(COOH).
Because of the joining of two carboxyl groups, this is one of the strongest organic acids.
Oxalic acid is recommended not to apply this in colonies with less than three frames, due to the deterioration of the cluster temperature balance in colonies where bees are weak.


When heat is applied on Oxalic acid dihydrate, Oxalic acid is a struggle with its sublimation property from solid state to gas state.
Oxalic acid occurs naturally in many foods.
Oxalic acid is an alpha,omega-dicarboxylic acid that is ethane substituted by carboxyl groups at positions 1 and 2.


Oxalic acid has a role as a human metabolite, a plant metabolite and an algal metabolite.
Oxalic acid has much greater acid strength than acetic acid.
Oxalic acid is a reducing agent and its conjugate base, known as oxalate (C2O2−4), is a chelating agent for metal cations.


Typically, oxalic acid occurs as the dihydrate with the formula C2H2O4·2H2O.
80% of kidney stones are formed from calcium oxalate.
Some Aspergillus species produce Oxalic acid, which reacts with blood or tissue calcium to precipitate calcium oxalate.


Oxalic acid dihydrate is a reducing agent.
Oxalic acid, also known as Oxalic acid is a diprotic acid, which means it can give away 2 protons (hydrogen ions) to a base.
Oxalic acid known as a constituent of wood sorrel as early as the 17th century, Oxalic acid was first prepared synthetically in 1776.


It is applied by mixing some oxalic acid into the sugar syrup prepared with warm water and dripping on the bees when the bee is in clusters and there are no closed brood at an outdoor temperature below 10 degrees.
While the amount of sugar and water in the solution remains the same, the Oxalic acid ratio may change according to the regional temperature.


In other words, the rates vary for each region.
Oxalic acid is a colourless crystalline solid that dissolves in water to give colorless acidic solutions.
Oxalic acid is classified as a dicarboxylic acid.


Oxalic acid is not metabolized but excreted in the urine.
Oxalic acid is used as an analytical reagent and general reducing agent.
Oxalic acid is recommended to apply this once a year.


Oxalic acid is a strong dicarboxylic acid.
Oxalic acid is recommended not to apply this in colonies with less than three frames, due to the deterioration of the cluster temperature balance in colonies where bees are weak.


When heat is applied to oxalic acid dihydrate, it is a struggle with its sublimation property from solid state to gas state.
Oxalic acid is a conjugate acid of an oxalate(1-) and an oxalate.
Oxalic acidis a relatively strong organic acid, being about 10,000 times stronger than acetic acid.


The di-anion, known as oxalate, is also a reducing agent as well as a ligand in coordination chemistry.
Oxalic acid is an odorless white solid chemical.
Oxalic acid can be found in powder or granule form.


In order to make these, there are evaporation apparatuses inside the hive, and oxalic acid is evaporated outside and sent into the hive through a pipe.
Oxalic acid is a common organic compound.
A range of living organisms — including fungi, bacteria, plants, animals, and humans — produce it.


Technically, oxalate occurs when the oxalic acid in plants binds to minerals.
However, many people use the terms interchangeably.
The body can either produce oxalate as a waste product or obtain it from the diet.


Oxalic acid occurs naturally in many foods.
Oxalic acid has much greater acid strength than acetic acid.
Although it can be readily purchased, Oxalic acid can be prepared in the laboratory by oxidizing sucrose using nitric acid in the presence of a small amount of vanadium pentoxide as a catalyst.


On a large scale, sodium oxalate is manufactured by absorbing carbon monoxide under pressure in hot sodium hydroxide.
Typically Oxalic acid is obtained as the dihydrate.
This solid can be dehydrated with heat or by azeotropic distillation.


Oxalate can combine with other minerals in the body to form compounds such as calcium oxalate and iron oxalate.
People can then eliminate these oxalate compounds in the urine or stool.
Oxalic acid is an organic compound.


Oxalic acid is a white crystalline solid that forms a colorless solution in water.
Leaves of the tea plant (Camellia sinensis) contain among the greatest measured concentrations of Oxalic acid relative to other plants.
Oxalic acid (CAS 6153-56-6), is an organic compound also known as Oxalic acid.
Oxalic acid forms a clear, colorless solution in water and has the chemical formula C2H2O4.



USES and APPLICATIONS of OXALIC ACID:
Oxalic acid is used in the dyeing process as a mordant
Oxalic acid is used in removing rust
In lanthanide chemistry, Oxalic acid is used as an important reagent


Oxalic acid is applied on marble sculptures to make it shine
Oxalic acid is used in the manufacture of dye
Oxalic acid has an industrial use resulting in manufacture of another substance (use of intermediates).


Oxalic acid is used in the following areas: building & construction work and formulation of mixtures and/or re-packaging.
Oxalic acid is used for the manufacture of: chemicals, , metals, machinery and vehicles and furniture.
Oxalic acid is used in bleaches


Oxalic acid is used in removing food and ink stains
Oxalic acid and its antimony salts are used as mordant in textile dyeing in industry.
Oxalic acid's usefulness in rust removal agents is that ferrous iron forms a stable, water-soluble salt with the ferrioxalate ion.


Oxalic acid is used in developing photographic film
Oxalic acid is used in wastewater treatment to remove the calcium deposit.
Oxalic acid is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.


Oxalic acid is used in the following products: coating products, polishes and waxes and washing & cleaning products.
Other release to the environment of Oxalic acid is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.


Other release to the environment of Oxalic acid is likely to occur from: outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).


Oxalic acid can be found in products with material based on: leather (e.g. gloves, shoes, purses, furniture).
Oxalic acid's main applications include cleaning or bleaching, especially for the removal of rust.
Oxalic acid's utility in rust removal agents is due to Oxalic acid's forming a stable, water-soluble salt with ferric iron, ferrioxalate ion.


Oxalic acid is used in the following products: non-metal-surface treatment products, metal surface treatment products, washing & cleaning products, coating products, metal working fluids, polishes and waxes, laboratory chemicals and pH regulators and water treatment products.
Oxalic acid is used in the following areas: building & construction work.


Oxalic acid is used for the manufacture of: furniture, , wood and wood products, pulp, paper and paper products and chemicals.
Other release to the environment of this substance is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.


Oxalic acid’s main applications include cleaning or bleaching, especially for the removal of rust.
Oxalic acid's utility in rust removal agents is due to its forming a stable, water-soluble salt with ferric iron, ferrioxalate ion.
Oxalic acid is used in the following products: pH regulators and water treatment products, washing & cleaning products, laboratory chemicals, non-metal-surface treatment products, metal surface treatment products, water softeners, water treatment chemicals and pharmaceuticals.


Release to the environment of Oxalic acid can occur from industrial use: formulation of mixtures, manufacturing of the substance, in the production of articles, as an intermediate step in further manufacturing of another substance (use of intermediates), formulation in materials, in processing aids at industrial sites and as processing aid.


Other release to the environment of Oxalic acid is likely to occur from: indoor use.
Oxalic acid is used in the following products: coating products, polishes and waxes and washing & leaning products.
Oxalic acid is used for the manufacture of: furniture, wood and wood products, pulp, paper and paper products and chemicals.


Oxalic acid is one of the organic compounds and occurs in various vegetables and plants.
Oxalic acid is used in the following products: pH regulators and water treatment products, laboratory chemicals, metal surface treatment products, leather treatment products, textile treatment products and dyes, non-metal-surface treatment products, washing & cleaning products, water softeners, water treatment chemicals and polymers.


Release to the environment of Oxalic acid can occur from industrial use: in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates), as processing aid, in the production of articles, formulation of mixtures and manufacturing of the substance.


Release to the environment of Oxalic acid can occur from industrial use: manufacturing of the substance, formulation of mixtures, as an intermediate step in further manufacturing of another substance (use of intermediates), formulation in materials, in processing aids at industrial sites, in the production of articles and as processing aid.


Oxalic acid is used to destroy warts.
Oxalic acid is used as a mordant in dyeing processes.
Dilute solutions (0.05–0.15 M) of Oxalic acid can be used to remove iron from clays such as kaolinite to produce light-colored ceramics.


Oxalic acid’s conjugate base is the hydrogen oxalate anion and its conjugate base (commonly known as oxalate) is a competitive lactate dehydrogenase (often abbreviated to LDH) enzyme inhibitor.
LDH catalyses the conversion of pyruvate to lactic acid (end product of the fermentation, which is an anaerobic process) oxidizing coenzyme NADH to NAD+ and H+ at the same time.


As a recommended surface pretreatment for stainless steels (surface etch) before application of solid metal or polymer self-lubricating coatings.
Restoring NAD+ levels is necessary if anaerobic energy metabolism is to continue through glycolysis.
Because cancer cells preferentially use anaerobic metabolism, LDH inhibition has been shown to inhibit tumour development and growth.


Thus, Oxalic acid provides an interesting possible course for the treatment of certain cancers.
Oxalic acid is sometimes used in the aluminum anodizing process, with or without sulfuric acid.
Compared to sulfuric acid anodizing, the coatings obtained are thinner and exhibit lower surface roughness.


Oxalic acid's main applications include cleaning or bleaching, especially for the removal of rust (iron complexing agent).
The two aqueous dihydrates of oxalic acid are used in alkalimetry and manganometry, rarely in the separation of earth metals and in the quantitative analysis of calcium.


Vaporized Oxalic acid, or a 6% solution of Oxalic acid in sugar syrup, is used by some beekeepers as an insecticide against the parasitic Varroa mite.
Oxalic acid is used for polishing stones and marble.
Effectively bleaches unfinished or stripped wood quickly and easily.


Instead of products containing heavy metals and residues, Oxalic acid hydrate from reliable places should be used.
Oxalic acid is also widely used as a wood bleach, most often in its crystalline form to be mixed with water to Oxalic acid's proper dilution for use.
Oxalic acid is used in the control of varroa in organic and conventional beekeeping in the food field.


Oxalic acid is used as bleach, especially for pulpwood.
Also, Oxalic acid is used in baking powder and as the third reagent in silica analysis instruments.
Oxalic acid is used as a cleaning chemical in coating processes.


Oxalic acid is used in the following products: pH regulators and water treatment products, laboratory chemicals, metal surface treatment products, leather treatment products, textile treatment products and dyes, non-metal-surface treatment products, washing & cleaning products, water softeners, water treatment chemicals and polymers.


Oxalic acid main applications include cleaning or bleaching (iron complexing agent), especially to remove rust.
Oxalic acid is widely used as an acid rinse in laundries, where Oxalic acid is effective in removing rust and ink stains because Oxalic acid converts most insoluble iron compounds into a soluble complex ion.


Oxalic acid naturally occurs in many plants and vegetables and is often used in freckle and bleaching cosmetic preparations.
Oxalic acid is the chief constituent of many commercial preparations used for removing scale from automobile radiators.
Oxalic acid is also used in bleaches, especially for pulpwood, and for rust removal and other cleaning, in baking powder, and as a third reagent in silica analysis instruments.


Oxalic acid's usefulness in rust removal agents is that ferrous iron forms a stable, water-soluble salt with the ferrioxalate ion.
In the beekeeping industry, Oxalic acid's evaporated form or Oxalic acid's 3.2% solution in sugar syrup can be used by some beekeepers as a killing agent against parasitic varroa mite.


Wood bleach - To bleach old and stained wood removing tannin stains and water stains
The cleaning product contains Oxalic acid.
Oxalic acid is an ingredient in some tooth whitening products.


About 25% of produced Oxalic acid will be used as a mordant in dyeing processes.
Niche uses: Oxalic acid is used by some beekeepers as a miticide against the parasitic varroa mite.
Oxalic acid is used in bleaches, especially for pulpwood.


Oxalic acid is also used in baking powder and as a third reagent in silica analysis instruments.
Oxalic acid is an important reagent in lanthanide chemistry.
Hydrated lanthanide oxalate forms readily in very strongly acidic solutions, in a densely crystallized, easily leached state, primarily free of contamination by non-lanthanide elements.


Oxalic acid, a pathogenicity factor for sclerotinia sclerotiorum, suppresses the Oxidative burst of the host plant and directly inhibits the OGA-stimulated production of H2O2 by soybean cells, even in the absence of other fungal components.
Thermal decomposition of this oxalate yields oxides, the most marketed form of these elements.


Oxalic acid is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Evaporated oxalic acid or a 3.2% solution of oxalic acid in sugar syrup is used by some beekeepers as a killer against parasitic insects.


Release to the environment of Oxalic acid can occur from industrial use: in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates), as processing aid, in the production of articles, formulation of mixtures and manufacturing of the substance.


Oxalic acid used in the control of varroa in honey bees is oxalic acid hydrate with the chemical formula C2H2O4 - 2H2O.
Instead of products containing heavy metals and residues, oxalic acid hydrate from reliable places should be used.
Oxalic acid is rubbed on the finished marble sculptures and seals the surface and adds shine.


Oxalic acid is used in the following products: non-metal-surface treatment products, metal surface treatment products, washing & cleaning products, coating products, metal working fluids, polishes and waxes, laboratory chemicals and pH regulators and water treatment products.
Oxalic acid is also used to clean iron and manganese deposits from quartz crystals.


Oxalic acid is used as a bleaching agent for leather and wood.
The two aqueous dihydrates of Oxalic acid are used in alkalimetry and manganometry, rarely in the separation of earth metals and in the quantitative analysis of calcium.


Oxalic acid is used as a bleach for wood to remove black stains caused by water penetration.
Oxalic acid dihydrate is a diprotic reducing agent used as a buffer
Oxalic acid is used to remove rust in the plumbing pipes and kitchen counters.


Oxalic acid is the main component of commercial rust removers used to remove metal rust stains from sinks and tubs.
Oxalic acid is used in bleaches, especially for pulpwood.
Oxalic acid is also used in baking powder and as a third reagent in silica analysis instruments.


Effectively bleaches unfinished or stripped wood quickly and easily.
Oxalic acid's also excellent for removing black water spots and tannin stains in wood.
Oxalic acid is used as a bleach for wood to remove black stains caused by water penetration.


Oxalic acid can also be used to freshen wood colour if Oxalic acid has become grayed due to external exposure.
Oxalic acid is widely used as an acid rinse in laundries, where it is effective in removing rust and ink stains because it converts most insoluble iron compounds into a soluble complex ion.


For the same reason, Oxalic acid is the chief constituent of many commercial preparations used for removing scale from automobile radiators.
Oxalic acid is used in the following areas: building & construction work.
Oxalic acid is used for the manufacture of: chemicals, metals, machinery and vehicles and furniture.


Rust removal- in removing rust on boats, in automotive shops and in restoring antiques in rust stain removal without harming Gel coat, fibre glass, steel and other metal surfaces for pre-treating stainless steel
For removing hard water stains from tiles and plumbing fixtures as a precipitator in rare earth mineral processing


Oxalic acid is an important reagent in Lanthanide chemistry.
Oxalic acid is used as a mordant in dyeing processes.
Oxalic acid is used as a rust remover in such applications as automotive shops and for the restoration of antiques.


Oxalic acid is a reducing agent and is used as a chelating agent with oxalate as its conjugate base.
Oxalic acid has an industrial use resulting in manufacture of another substance (use of intermediates).
Oxalic acid is used in the following areas: building & construction work and formulation of mixtures and/or re-packaging.


Oxalic acid and Oxalic acid's antimony salts are used as mordant in textile dyeing in industry.
Oxalic acid is used in the control of varroa in organic and conventional beekeeping in the food field.
Available in various quantities, purities, and reagent grades; used as a mordant, acid rinse, rust removal agent, bleach component, lanthanide chemistry reagent, etc.


Oxalic acid can be used to clean minerals like many other acids.
Two such examples are quartz crystals and pyrite.
Oxalic acid is sometimes used in the aluminum anodizing process, with or without sulfuric acid.


Compared to sulfuric acid anodizing, the coatings obtained are thinner and exhibit lower surface roughness.
Oxalic acid’s also excellent for removing black water spots and tannin stains in wood.
Oxalic acid is Suitable for outdoor use.


Oxalic acid is also widely used as a wood bleach, most often in its crystalline form to be mixed with water to its proper dilution for use.
Oxalic acid is necessary to use appropriate strippers and cleaners to remove coatings.
In wood restorers where the acid dissolves away a layer of dry surface wood to expose fresh material underneath.


Oxalic acid is also sometimes used in the aluminum anodizing process, with or without sulfuric acid.
Compared to the sulfuric acid anodizing, the coatings obtained are thinner and exhibit a lower surface roughness.
Oxalic acid is Suitable for outdoor use.


Oxalic acid is used as a mordant in dyeing processes.
Oxalic acid's main applications include cleaning or bleaching, especially for the removal of rust (iron complexing agent).
Its utility in rust removal agents is due to its forming a stable, water-soluble salt with ferric iron, ferrioxalate ion.


There are many Oxalic acid applications that we can take from various sources.
Up to 25% of Oxalic acid produced will be used as a mordant in dyeing processes.
There are various uses of Oxalic acid and the most significant one is in the cleaning industry i.e. in places like laundries, bleaching, dyeing, etc


Oxalic acid is an ingredient in some tooth whitening products.
About 25% of produced oxalic acid will be used as a mordant in dyeing processes.
Oxalic acid is used to clean minerals.


Other release to the environment of Oxalic acid is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use
Oxalic acid is a strong dicarboxylic acid occurring in many plants and vegetables and can be used as an analytical reagent and general reducing agent.


Oxalic acid is also used in bleaches, especially for pulpwood, and for rust removal and other cleaning, in baking powder, and as a third reagent in silica analysis instruments.
Oxalic acid plays a key role in the interaction between pathogenic fungi and plants.


Other release to the environment of Oxalic acid is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.
Oxalic acid is widely used in laundry to effectively remove ink stains and in industries for the removal of rust.


For the same reason, Oxalic acid is the main component of many commercial preparations used to remove scale from car radiators.
Oxalic acid is used in the synthesis of cleaning products.
Oxalic acid is also used as a marble polishing and grinding agent.


Oxalic acid is used together with stearic acid in the production of marble polishing powder.
Oxalic acid is used as a grinding agent in preparing & polishing stones & marble in restoring furniture
Oxalic acid can be used as a reducing agent in photography.


Small amounts of oxalic acid enhances plant resistance to fungi, but higher amounts cause widespread programmed cell death of the plant and help with fungi infection.
Plants normally produce it in small amounts, but some pathogenic fungi such as Sclerotinia sclerotiorum cause a toxic accumulation.


Oxalic acid's utility in rust removal agents is due to Oxalic acid's forming a stable, water-soluble salt with ferric iron, ferrioxalate ion.
Oxalate, besides being biosynthesised, may also be biodegraded.
Oxalobacter formigenes is an important gut bacterium that helps animals (including humans) degrade oxalate.


Oxalic acid is a relatively strong organic acid with many commercial uses especially in the carpentry and joinery trades in the UK.
Oxalic acid is also used to clean iron and manganese deposits from quartz crystals.
In the refinishing of wooden furniture, Oxalic acid can be used after stripping to lighten darker stained areas.


Oxalic acid can also be used as a rust remover and a stain remover in many other applications.
When using on wood the wood must be free of all coatings, waxes & oils.
Oxalic acid is used as an additive to automotive wheel cleaners.


Oxalic acid is used as a mordant in dyeing processes.
Evaporated Oxalic acid or a 3.2% solution of Oxalic acid in sugar syrup is used by some beekeepers as a killer against parasitic insects.
Oxalic acid is used to clean minerals.


Oxalic acid main applications include cleaning or bleaching (iron complexing agent), especially to remove rust.
Oxalic acid is rubbed on the finished marble sculptures and seals the surface and adds shine.
Oxalic acid is used as a buffer in chromatographic separation, dechelation and deproteinization in tandem with acetonitrile and/or other solvents.
Oxalic acid is generally used as a mordant, reducing agent and bleaching agent for the dyeing and printing industry.


-Industrial use of Oxalic acid:
In industry, Oxalic acid is primarily used in mineral processing mechanisms.
In addition, Oxalic acid can be used to sterilize equipment, and people in the textile industry use Oxalic acid to bleach clothes.
Oxalic acid is also used in factories for removing rust from metallic equipment.


-Niche uses:
Oxalic acid is used by some beekeepers as a miticide against the parasitic varroa mite.
Dilute solutions (0.05–0.15 M) of oxalic acid can be used to remove iron from clays such as kaolinite to produce light-colored ceramics.


-The polishing powder obtained is applied on the marble and processed.
A chemical reaction occurs.
After polishing, polishing is done.
In this way, it protects the marble against external effects for a long time.


-Semiconductor industry:
Oxalic acid is also used in electronic and semiconductor industries.
In 2006 Oxalic acid was reported being used in electrochemical–mechanical planarization of copper layers in the semiconductor devices fabrication process.


-How to use Oxalic acid:
Prepare a solution by dissolving 60g of Oxalic acid in 1 litre of water, apply to stain or rust and allow to work for 20-30 minutes.
Always rinse thoroughly with clean water.
For wood bleaching it is recommended to neutralize after treatment with a borax solution (3 tablespoons of borax dissolved in 1 litre of water).


-Removing marks, stains and rust:
Oxalic acid is mainly used for the most demanding cleaning operations.
Oxalic acid effectively removes all kinds of marks and stains from the surface of the object.
Oxalic acid is a gentle stain remover that eats up stains but leaves the base as it is.
Acids have similar properties to bleach and can be used, for example, to remove rust on metals such as plumbing pipes, kitchen countertops etc.
Some cleaning agents, laundry detergents, and bleaches contain some of this acid.
Oxalic acid is also ideal for polishing virtually all stones and disposing of waste wood.


-Semiconductor industry:
Oxalic acid is also used in electronic and semiconductor industries.
In 2006 it was reported being used in electrochemical–mechanical planarization of copper layers in the semiconductor devices fabrication process


-Extractive Metallurgy:
Oxalic acid is a primary reagent in lanthanide chemistry.
Hydrated lanthanide oxalates readily form in very strongly acidic solutions in easily filtered form, a densely crystalline, and as largely free of contamination by non-lanthanide elements.
This oxalate thermal decomposition gives the oxides, the most commonly marketed form of these elements.


-Uses of Oxalic acid:
*Metal Cleaner
*Radiator Cleaner
*Leather Tanning
*Bleaching Agent
*Rust Remover
*Stain & Ink Remover


-Medical use of Oxalic acid:
In the medical field, companies use acids to further purify or dilute certain chemicals.
However, there is little data on the health benefits of Oxalic acid.
-Oxalic acid is mainly used as a reducing element in the development of photographic film.
-Oxalic acid is also used in wastewater treatment plants to effectively remove lime from water.


-Oxalic acid is used:
*Oxalic Acid 99.6% Purifying agent in pharmaceutical industry, special in antibiotic medication, such as oxytetracycline,Chloramphenicol etc;
*Oxalic Acid 99.6% Precipitating agent in Rare-earth mineral processing;
*Bleaching agent in the textile activities, wood pulp bleaching;
Rust-remover for metal treatment;
*Oxalic Acid 99.6% Grinding agent, such as marble polishing;
*Oxalic Acid 99.6% Waste water treatment, removing calcium from water.


-Cleaning:
Oxalic acid application mainly includes bleaching or cleaning, especially Oxalic acid as a rust remover (an iron complexing agent).
Oxalic acid's utility in rust removal agents is because Oxalic acid forms a stable, water-soluble salt with ferrioxalate ion and ferric iron.



PREPARATION of OXALIC ACID:
Oxalic acid is mainly manufactured by the oxidation of carbohydrates or glucose using nitric acid or air in the presence of vanadium pentoxide.
A variety of precursors can be used including glycolic acid and ethylene glycol.
A newer method entails oxidative carbonylation of alcohols to give the diesters of Oxalic acid:

4 ROH + 4 CO + O2 → 2 (CO2R)2 + 2 H2O
These diesters are subsequently hydrolyzed to Oxalic acid.
Approximately 120,000 tonnes are produced annually.

Historically Oxalic acid was obtained exclusively by using caustics, such as sodium or potassium hydroxide, on sawdust, followed by acidification of the oxalate by mineral acids, such as sulfuric acid.
Oxalic acid can also be formed by the heating of sodium formate in the presence of an alkaline catalyst.



WHAT IS OXALIC ACID USED FOR?
Although oxalic acid naturally occurs in plants and humans, it also has a variety of uses in industry.
These uses include:
*removing rust
*removing stains
*stripping and cleaning
*removing wax
*cleaning wood
*dyeing textiles
Laboratories may also use oxalic acid and oxalate salts as anticoagulants in blood specimens.



LABORATORY METHODS of OXALIC ACID:
Although Oxalic acid can be readily purchased, Oxalic acid can be prepared in the laboratory by oxidizing sucrose using nitric acid in the presence of a small amount of vanadium pentoxide as a catalyst.

The hydrated solid can be dehydrated with heat or by azeotropic distillation.
Developed in the Netherlands, an electrocatalysis by a copper complex helps reduce carbon dioxide to Oxalic acid; this conversion uses carbon dioxide as a feedstock to generate Oxalic acid.

Anhydrous Oxalic acid exists as two polymorphs; in one the hydrogen-bonding results in a chain-like structure, whereas the hydrogen bonding pattern in the other form defines a sheet-like structure.
Because the anhydrous material is both acidic and hydrophilic (water seeking), it is used in esterifications.



HISTORY of OXALIC ACID:
The preparation of salts of Oxalic acid (crab acid) from plants had been known, at least since 1745, when the Dutch botanist and physician Herman Boerhaave isolated a salt from wood sorrel.
By 1773, François Pierre Savary of Fribourg, Switzerland had isolated Oxalic acid from its salt in sorrel.

In 1776, Swedish chemists Carl Wilhelm Scheele and Torbern Olof Bergman produced Oxalic acid by reacting sugar with concentrated nitric acid; Scheele called the acid that resulted socker-syra or såcker-syra (sugar acid).
By 1784, Scheele had shown that "sugar acid" and Oxalic acid from natural sources were identical.

In 1824, the German chemist Friedrich Wöhler obtained Oxalic acid by reacting cyanogen with ammonia in aqueous solution.
This experiment may represent the first synthesis of a natural product.



DIHYDRATE:
The dihydrate H2C2O4.2H2O has space group C52h–P21/n, with lattice parameters a = 611.9 pm, b = 360.7 pm, c = 1205.7 pm, β = 106°19', Z = 2.
The main inter-atomic distances are: C−C 153 pm, C−O1 129 pm, C−O2 119 pm.

Theoretical studies indicate that Oxalic acid dihydrate is one of very few crystalline substances that exhibit negative area compressibility.
Namely, when subjected to isotropic tension stress (negative pressure), the a and c lattice parameters increase as the stress decreases from −1.17 GPa to −0.12 GPa and from −1.17 GPa to −0.51 GPa, respectively.



PREPARATION OF OXALIC ACID:
Oxalic acid is mainly manufactured by the oxidation of carbohydrates or glucose using nitric acid or air in the presence of vanadium pentoxide.
A variety of precursors can be used including glycolic acid and ethylene glycol.
A newer method entails oxidative carbonylation of alcohols to give the diesters of oxalic acid:

4 ROH + 4 CO + O2 → 2 (CO2R)2 + 2 H2O
These diesters are subsequently hydrolyzed to oxalic acid. Approximately 120,000 tonnes are produced annually.
Historically oxalic acid was obtained exclusively by using caustics, such as sodium or potassium hydroxide, on sawdust, followed by acidification of the oxalate by mineral acids, such as sulfuric acid.
Oxalic acid can also be formed by the heating of sodium formate in the presence of an alkaline catalyst.



LABORATORY METHODS OF OXALIC ACID:
Although it can be readily purchased, oxalic acid can be prepared in the laboratory by oxidizing sucrose using nitric acid in the presence of a small amount of vanadium pentoxide as a catalyst.
The hydrated solid can be dehydrated with heat or by azeotropic distillation.
Developed in the Netherlands, an electrocatalysis by a copper complex helps reduce carbon dioxide to oxalic acid; this conversion uses carbon dioxide as a feedstock to generate oxalic acid.



STRUCTURE OF OXALIC ACID:
Anhydrous:
Anhydrous oxalic acid exists as two polymorphs; in one the hydrogen-bonding results in a chain-like structure, whereas the hydrogen bonding pattern in the other form defines a sheet-like structure.
Because the anhydrous material is both acidic and hydrophilic (water seeking), it is used in esterifications.



OXALIC ACID FORMULA:
Oxalic acid is a dicarboxylic acid with the chemical formula C2H2O4. Oxalic acid occurs in the cell sap of Oxalis and Rumex species of plants as potassium and calcium salt.
In an aqueous solution, oxalic acid is a weak acid that will only partially ionise.
Oxalic acid has two acidic protons.
The initial ionisation yields HC2O4-, a weak acid that will ionise as well.
Oxalic acid is one of the most powerful of the organic acids and expels carbonic acid and many other acids from their salts.
Oxalic acid is produced by the action of either hydrate of potash or of nitric acid upon most organic compounds of natural occurrence.
Oxalic acid is also called diprotic acid.



OXALIC ACID OCCURS NATURALLY IN MANY PLANTS LIKE THE FOLLOWING:
*Fruits
*Cocoa
*Leafy green vegetables
*Nuts
*Seeds
*Spinach
*Sweet potatoes
*Star fruit
*Turnip greens
*Endive
*Swiss chard
*Beet greens



EQUIVALENT WEIGHT OF OXALIC ACID (CALCULATION):
The molar mass of hydrated oxalic acid is 126 grams per mole.
Since the chemical formula of this compound can be written as COOH-COOH, it can be understood that oxalic acid is a dibasic acid which has the ability to donate two H+ ions.

Therefore, the equivalent weight of oxalic acid can be calculated with the help of the following formula:
Equivalent weight = (molecular weight)/(number of equivalent moles)

Since 1 mole of oxalic acid can release 2 moles of H+ ions and neutralize 2 moles of OH– ions, the number of equivalent moles here is equal to 2.
Thus, the equivalent weight of oxalic acid can be calculated as follows:

Equivalent mass of oxalic acid = molecular mass of oxalic acid/2 = 126g/2 = 63 grams.
Therefore, the equivalent weight of oxalic acid is 63 grams.



OXALIC ACID STRUCTURE:
In its anhydrous form, Oxalic acid can be noted that oxalic acid exists in two different polymorphs.
In the first polymorph of oxalic acid, hydrogen bonding takes place.

Due to this hydrogen bonding, a chain-like structure is developed at the intermolecular level.
The second polymorph of Oxalic acid is also subject to hydrogen bonding.
However, in this case, the hydrogen bonding attributes a sheet-like structure to Oxalic acid at the intermolecular level.

Oxalic acid is widely used in esterification reactions owing to two important properties.
The first property that makes oxalic acid ideal for esterification reactions is its acidic nature.
The second and most important property of oxalic acid is its hydrophilic nature (it tends to seek water).



PREPARATION OF OXALIC ACID:
Oxalic acid can be easily prepared by oxidation of certain carbohydrates like sucrose by concentrating nitric acid.
During oxidation, the carbon atoms are split off in pairs giving oxalic acid.



PRODUCTION OF OXALIC ACID:
Oxalic acid is mainly produced by the oxidation of carbohydrates or glucose in the presence of vanadium pentoxide using nitric acid or air.
Various precursors can be used, including glycolic acid and ethylene glycol.
A newer method requires oxidative carbonylation of alcohols to yield oxalic acid diesters.

4 ROH + 4 CO + 02 → 2 (CO2R) 2 + 2H20

Oxalic acid is one of the most well-known plant-derived organic acids.
Oxalic acid, which is shown with the chemical formula COOH2, is found in nature as a calcium salt in the rhubarb plant, in the plant called sorrel as the sodium salt, and in the sap of some plants.
Most plant sources contain this organic acid.

Plants such as spinach, tomatoes, sorrel are in it.
Because it is an acid, it can form a salt with an ion in the environment.
Oxalic acid, which enters a biologically living system and body, forms salts with ions there.
Calcium oxalate, which is the most common salt, accumulates in the body, usually in the urinary system, especially in the kidneys, causing stone formation.



PRODUCTION OF OXALIC ACID BY FUNGI:
Many soil fungus species secrete oxalic acid, resulting in greater solubility of metal cations, increased availability of certain soil nutrients, and can lead to the formation of calcium oxalate crystals.
Some fungi such as Aspergillus niger have been extensively studied for the industrial production of oxalic acid; however, those processes are not yet economically competitive with production from oil and gas.



BIOCHEMISTRY of OXALIC ACID:
The conjugate base of Oxalic acid is the hydrogenoxalate anion, and Oxalic acid's conjugate base (oxalate) is a competitive inhibitor of the lactate dehydrogenase (LDH) enzyme.

LDH catalyses the conversion of pyruvate to lactic acid (end product of the fermentation (anaerobic) process) oxidising the coenzyme NADH to NAD+ and H+ concurrently.
Restoring NAD+ levels is essential to the continuation of anaerobic energy metabolism through glycolysis.

As cancer cells preferentially use anaerobic metabolism (see Warburg effect) inhibition of LDH has been shown to inhibit tumor formation and growth, thus is an interesting potential course of cancer treatment.

Oxalic acid plays an key role in the interaction between pathogenic fungi and plants.
Small amounts of Oxalic acid enhances plant resistance to fungi, but higher amounts cause widespread programmed cell death of the plant and help with fungi infection.

Plants normally produce Oxalic acid in small amounts, but some pathogenic fungi such as Sclerotinia sclerotiorum cause a toxic accumulation.
Oxalate, besides being biosynthesised, may also be biodegraded.
Oxalobacter formigenes is an important gut bacteria that helps animals (including humans) degrade oxalate.



REACTIONS OF OXALIC ACID:
Acid-base properties:
Oxalic acid's pKa values vary in the literature from 1.25–1.46 and 3.81–4.40.
The 100th ed of the CRC, released in 2019, has values of 1.25 and 3.81.
Oxalic acid is relatively strong compared to other carboxylic acids:

C2O4H2 ⇌ C2O4H− + H+ pKa = 1.27
C2O4H− ⇌ C2O2−4 + H+ pKa = 4.27
Oxalic acid undergoes many of the reactions characteristic of other carboxylic acids.
Oxalic acid forms esters such as dimethyl oxalate (m.p. 52.5 to 53.5 °C, 126.5 to 128.3 °F).
Oxalic acid forms an acid chloride called oxalyl chloride.



METAL-BINDING PROPERTIES OF OXALIC ACID:
Transition metal oxalate complexes are numerous, e.g. the drug oxaliplatin.
Oxalic acid has shown to reduce manganese dioxide MnO
2 in manganese ores to allow the leaching of the metal by sulfuric acid.

Oxalic acid is an important reagent in lanthanide chemistry.
Hydrated lanthanide oxalates form readily in very strongly acidic solutions as a densely crystalline, easily filtered form, largely free of contamination by nonlanthanide elements:

2 Ln3+ + 3 C2O4H2 → Ln2(C2O4)3 + 6 H+
Thermal decomposition of these oxalates gives the oxides, which is the most commonly marketed form of these elements.



OTHER:
Oxalic acid and oxalates can be oxidized by permanganate in an autocatalytic reaction.
Oxalic acid vapor decomposes at 125–175 °C into carbon dioxide CO
2 and formic acid HCOOH.
Photolysis with 237–313 nm UV light also produces carbon monoxide CO and water.

Evaporation of a solution of urea and oxalic acid in 2:1 molar ratio yields a solid crystalline compound H
2C2O4.[CO(NH2)2]2, consisting of stacked two-dimensional networks of the neutral molecules held together by hydrogen bonds with the oxygen atoms.



OCCURRENCE of OXALIC ACID:
Biosynthesis:
At least two pathways exist for the enzyme-mediated formation of oxalate.

In one pathway, oxaloacetate, a component of the Krebs citric acid cycle, is hydrolyzed to oxalate and acetic acid by the enzyme oxaloacetase:
[O2CC(O)CH2CO2]2− + H2O → C2O2−4 + CH3CO−2 + H+
It also arises from the dehydrogenation of glycolic acid, which is produced by the metabolism of ethylene glycol.

Oxalic acid and oxalates are abundantly present in many plants, most notably fat hen (lamb's quarters), sour grass, and sorrel (including Oxalis).
The root and/or leaves of rhubarb and buckwheat are listed being high in Oxalic acid.

Foods that are edible but that still contain significant concentrations of Oxalic acid include—in decreasing order—star fruit (carambola), black pepper, parsley, poppy seed, rhubarb stalks, amaranth, spinach, chard, beets, cocoa, chocolate, most nuts, most berries, and beans.
The gritty “mouth feel” one experiences when drinking milk with a rhubarb dessert is caused by precipitation of calcium oxalate.
Thus even dilute amounts of Oxalic acid can readily "crack" the casein found in various dairy products.



OCCURRENCE IN FOODS AND PLANTS of OXALIC ACID:
Early investigators isolated Oxalic acid from wood-sorrel (Oxalis).
Members of the spinach family and the brassicas (cabbage, broccoli, brussels sprouts) are high in oxalates, as are sorrel and umbellifers like parsley.

The leaves and stems of all species of the genus Chenopodium and related genera of the family Amaranthaceae, which includes quinoa, contain high levels of Oxalic acid.
Rhubarb leaves contain about 0.5% Oxalic acid, and jack-in-the-pulpit (Arisaema triphyllum) contains calcium oxalate crystals.

Similarly, the Virginia creeper, a common decorative vine, produces Oxalic acid in its berries as well as oxalate crystals in the sap, in the form of raphides.
Bacteria produce oxalates from oxidation of carbohydrates.

Plants of the genus Fenestraria produce optical fibers made from crystalline Oxalic acid to transmit light to subterranean photosynthetic sites.
Carambola, also known as starfruit, also contains Oxalic acid along with caramboxin.
Citrus juice contains small amounts of Oxalic acid.

Citrus fruits produced in organic agriculture contain less Oxalic acid than those produced in conventional agriculture.
The formation of naturally occurring calcium oxalate patinas on certain limestone and marble statues and monuments has been proposed to be caused by the chemical reaction of the carbonate stone with Oxalic acid secreted by lichen or other microorganisms.

Production by fungi:
Many soil fungus species secrete Oxalic acid, resulting in greater solubility of metal cations, increased availability of certain soil nutrients, and can lead to the formation of calcium oxalate crystals.
Some fungi such as Aspergillus niger have been extensively studied for the industrial production of Oxalic acid; however, those processes are not yet economically competitive with production from oil and gas.



ALTERNATIVE PARENTS of OXALIC ACID:
*Carboxylic acids
*Organic oxides
*Hydrocarbon derivatives
*Carbonyl compounds



SUBSTITUENTS of OXALIC ACID:
*Dicarboxylic acid or derivatives
*Carboxylic acid
*Organic oxygen compound
*Organic oxide
*Hydrocarbon derivative
*Organooxygen compound
*Carbonyl group
*Aliphatic acyclic compound



PHYSICAL and CHEMICAL PROPERTIES of OXALIC ACID:
Chemical formula: C2H2O4
Molar mass: 90.034 g·mol−1 (anhydrous)
126.065 g·mol−1 (dihydrate)
Appearance: White crystals
Odor: Odorless
Density: 1.90 g·cm3 (anhydrous, at 17 °C)
1.653 g·cm−3 (dihydrate)
Melting point: 189 to 191 °C (372 to 376 °F; 462 to 464 K)
101.5 °C (214.7 °F; 374.6 K) dihydrate
Solubility in water: 46.9 g/L (5 °C), 57.2 (10 °C),
75.5 (15 °C), 95.5 (20 °C), 118 (25 °C), 139 (30 °C),
178 (35 °C), 217 (40 °C), 261 (45 °C), 315 (50 °C),
376 (55 °C), 426 (60 °C), 548 (65 °C)
Solubility: 237 g/L (15 °C) in ethanol
14 g/L (15 °C) in diethyl ether
Vapor pressure: Acidity (pKa): 1.25, 4.14
Conjugate base: Hydrogenoxalate
Magnetic susceptibility (χ): −60.05·10−6 cm3/mol
Heat capacity (C): 91.0 J·mol−1·K−1
Std molar entropy (S⦵298): 109.8 J·mol−1·K−1
Std enthalpy of formation (ΔfH⦵298): −829.9 kJ·mol−1

Molecular Weight: 90.03 g/mol
XLogP3-AA: -0.3
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 1
Exact Mass: 89.99530854 g/mol
Monoisotopic Mass: 89.99530854 g/mol
Topological Polar Surface Area: 74.6Ų
Heavy Atom Count: 6
Formal Charge: 0
Complexity: 71.5
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Physical state: crystalline
Color: white
Odor: odorless

Melting point/freezing point:
Melting point/range: 189,5 °C - dec.
Initial boiling point and boiling range: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: No data available
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: 1,3 at 9 g/l
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: No data available
Partition coefficient: n-octanol/water: No data available
Vapor pressure: No data available
Density: 1,9 g/cm3 at 20 °C
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: none
Other safety information: No data available

Molecular Weight: 90.03
Molecular Weight: 90.03
XLogP3-AA: -0.3
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 1
Exact Mass: 89.99530854
Monoisotopic Mass: 89.99530854
Topological Polar Surface Area: 74.6 Ų
Heavy Atom Count: 6
Formal Charge: 0
Complexity: 71.5
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0

Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Appearance Form: powder
Color: white
Odor: odorless
Odor Threshold: Not applicable
pH: 1,3 at 9 g/l
Melting point/freezing point:
Melting point/range: 189,5 °C - dec.
Initial boiling point and boiling range: No data available
Flash point: No data available
Evaporation rate: No data available
Flammability (solid, gas): No data available
Upper/lowe flammability or explosive limits: No data available
Vapor pressure: No data available
Vapor density: No data available

Relative density: No data available
Water solubility: No data available
Partition coefficient: n-octanol/water: No data available
Autoignition temperature: No data available
Decomposition temperature: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Explosive properties: No data available
Oxidizing properties: No data available
Other safety information: No data available
Molecular Formula: C2H6O6
Average mass: 126.065 Da
Monoisotopic mass: 126.016441 Da
Boiling point: 149 - 160 °C (1013 hPa) (decomposition)
Density 1.65 g/cm3 (20 °C)

Flash point: 157 °C (decomposition)
Melting Point: 98 - 100 °C
pH value: 1.5 (10 g/l, H₂O)
Vapor pressure: 0.000312 hPa (25 °C)
Bulk density: 813 kg/m3
Solubility: >100 g/l
Chemical formula: C2H2O4
Molar mass: 90.034 g•mol−1 (anhydrous), 126.065 g•mol−1 (dihydrate)
Appearance: White crystals
Odor: odorless
Density: 1.90 g•cm−3 (anhydrous, at 17 °C), 1.653 g•cm−3 (dihydrate)
Melting point: 189 to 191 °C, 101.5 °C (214.7 °F; 374.6 K) dihydrate
Solubility in water: 90-100 g/L (20 °C)
Solubility: 237 g/L (15 °C) in ethanol, 14 g/L (15 °C) in diethyl ether
Vapor pressure: Acidity (pKa): 1.25, 4.14
Conjugate base: Hydrogenoxalate
Magnetic susceptibility (χ): -60.05•10−6 cm3/mol



FIRST AID MEASURES of OXALIC ACID:
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Consult a physician.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Immediately call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of OXALIC ACID:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of OXALIC ACID:
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of OXALIC ACID:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles.
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
protective clothing
-Control of environmental exposure:
Do not let product enter drains



HANDLING and STORAGE of OXALIC ACID:
-Precautions for safe handling:
*Advice on safe handling:
Work under hood.
*Hygiene measures:
Immediately change contaminated clothing.
Wash hands and face after working with substance.
-Conditions for safe storage, including any incompatibilities:
Storage conditions
Tightly closed.
Dry.



STABILITY and REACTIVITY of OXALIC ACID:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Conditions to avoid:
no information available
-Incompatible materials:
No data available



SYNONYMS:
Oxalic acid
Ethanedioic acid
Wood bleach
Crab Acid
(Carboxyl)carboxylic acid
Carboxylformic acid
Dicarboxylic acid
Diformic acid
[Ethanedioato(2-)-?O1,?O2]-magnesium
144-62-7
1o4n
1t5a
2dua
2hwg
4-02-00-01819 (Beilstein Handbook Reference)
48J
745-EP2269610A2
745-EP2269989A1
745-EP2269990A1
745-EP2270002A1
745-EP2270006A1
745-EP2270011A1
745-EP2270113A1
745-EP2270505A1
745-EP2272516A2
745-EP2272537A2
745-EP2272827A1
745-EP2272837A1
745-EP2272847A1
745-EP2275404A1
745-EP2275410A1
745-EP2275411A2
745-EP2275412A1
745-EP2275424A1
745-EP2277622A1
745-EP2277848A1
745-EP2277858A1
745-EP2277866A1
745-EP2277867A2
745-EP2280000A1
745-EP2280003A2
745-EP2280008A2
745-EP2280010A2
745-EP2280012A2
745-EP2281563A1
745-EP2281823A2
745-EP2284149A1
745-EP2284160A1
745-EP2284169A1
745-EP2284178A2
745-EP2284179A2
745-EP2286811A1
745-EP2287147A2
745-EP2287152A2
745-EP2287157A1
745-EP2287160A1
745-EP2287161A1
745-EP2287162A1
745-EP2289510A1
745-EP2289876A1
745-EP2289877A1
745-EP2289879A1
745-EP2289883A1
745-EP2289894A2
745-EP2292227A2
745-EP2292234A1
745-EP2292593A2
745-EP2292597A1
745-EP2292618A1
745-EP2292624A1
745-EP2295401A2
745-EP2295402A2
745-EP2295406A1
745-EP2295414A1
745-EP2295416A2
745-EP2295424A1
745-EP2295426A1
745-EP2295427A1
745-EP2295433A2
745-EP2298731A1
745-EP2298734A2
745-EP2298735A1
745-EP2298739A1
745-EP2298747A1
745-EP2298748A2
745-EP2298755A1
745-EP2298758A1
745-EP2298759A1
745-EP2298763A1
745-EP2298768A1
745-EP2298772A1
745-EP2298780A1
745-EP2301544A1
745-EP2301922A1
745-EP2301931A1
745-EP2301937A1
745-EP2305219A1
745-EP2305257A1
745-EP2305633A1
745-EP2305636A1
745-EP2305641A1
745-EP2305651A1
745-EP2305655A2
745-EP2305664A1
745-EP2305669A1
745-EP2305672A1
745-EP2305673A1
745-EP2305675A1
745-EP2305676A1
745-EP2305679A1
745-EP2305680A2
745-EP2305683A1
745-EP2305689A1
745-EP2308839A1
745-EP2308849A1
745-EP2308850A1
745-EP2308854A1
745-EP2308857A1
745-EP2308861A1
745-EP2308869A1
745-EP2308872A1
745-EP2308873A1
745-EP2308875A1
745-EP2311801A1
745-EP2311802A1
745-EP2311803A1
745-EP2311808A1
745-EP2311809A1
745-EP2311810A1
745-EP2311811A1
745-EP2311814A1
745-EP2311822A1
745-EP2311824A1
745-EP2311829A1
745-EP2311831A1
745-EP2311834A1
745-EP2311835A1
745-EP2311837A1
745-EP2311839A1
745-EP2314295A1
745-EP2314574A1
745-EP2314576A1
745-EP2314581A1
745-EP2314585A1
745-EP2314586A1
745-EP2314588A1
745-EP2314589A1
745-EP2314593A1
745-EP2316457A1
745-EP2316458A1
745-EP2316459A1
745-EP2316825A1
745-EP2316826A1
745-EP2316827A1
745-EP2316828A1
745-EP2316829A1
745-EP2316831A1
745-EP2316834A1
745-EP2316835A1
745-EP2316836A1
745-EP2316837A1
745-EP2371811A2
745-EP2371814A1
745-EP2374454A1
745-EP2374526A1
745-EP2374780A1
745-EP2374781A1
745-EP2374895A1
9E7R5L6H31
Acidum oxalicum
AI3-26463
AKOS005449445
Aktisal
Anhydrous oxalic acid
Aquisal
BBL003000
BDBM14674
bis((2R)-azetidine-2-carbonitrile)
bis(1-(3-methyloxetan-3-yl)ethan-1-amine)
bis(5-azaspiro[2.5]octan-8-ol)
bmse000106
BP-21133
BRN 0385686
C00209
C2-H2-O4
C2-H2-O4.Mg
C2H2O4
C2H2O4.Mg
CAS-144-62-7
Caswell No. 625
CCG-266020
CCRIS 1454
CHEBI:16995
CHEMBL146755
CS-0013716
D0U7BY
DB03902
DTXCID805816
DTXSID0025816
EC 205-634-3
EC 271-678-5
EINECS 205-634-3
EINECS 271-678-5
EN300-16428
EPA Pesticide Chemical Code 009601
Ethandisaeure
Ethane-1,2-dioate
Ethane-1,2-dioic acid
ethanedioic acid
Ethanedioic acid (9CI)
Ethanedioic acid, uranium(4) salt (2:1)
Ethanedionate
Ethanedionic acid
F1B1B2D7-C290-4CE6-8550-F25B202AFADE
F2191-0257
FT-0657506
H2ox
HOOCCOOH
HSDB 1100
HY-Y0262
J-007978
oxalic acid
ethanedioic acid
Aktisal
Aquisal
oxalate
Oxiric acid
Oxalsaeure
Oxaalzuur
Kyselina stavelova
Acide oxalique
Acido ossalico
Acidum oxalicum
Caswell No. 625
Oxalicacid
NCI-C55209
Ethanedionic acid
Ethane-1,2-dioic acid
CCRIS 1454
EPA Pesticide Chemical Code 009601
HSDB 1100
AI3-26463
NSC 62774
UNII-9E7R5L6H31
BRN 0385686
HOOCCOOH
C2H2O4
Oxalic acid anhydrous
CHEBI:16995
9E7R5L6H31
C2-beta-polymorph
ETHANEDIOIC ACID DIHYDRATE
Ethanedioic acid-d2
Oxalic Acid Dianion
DSSTox_CID_5816
C00209
DSSTox_RID_77935
DSSTox_GSID_25816
Oxalic acid diammonium salt
Wood bleach
OXD
NSC115893
Ethandisaeure
Ethanedionate
Oxagel
2dua
2hwg
H2ox
Anhydrous oxalic acid
Ethane-1,2-dioate
Oxalic acid, 98%
Oxalic acid (8CI)
oxalic acid 2 hydrate
Oxalic acid, anhydrous
Oxalic acid 2-Hydrate
1o4n
1t5a
Oxalate standard for IC
WLN: QVVQ
Ethanedioic acid (9CI)
Oxalic acid dihydrate ACS
Ultraplast Activate S 52
bmse000106
Oxalic Acid Low Ash Grade
NCIOpen2_000770
NCIOpen2_001022
NCIOpen2_001042
NCIOpen2_001202
NCIOpen2_008831
TETRADECANOIC-D27ACID
4-02-00-01819 (Beilstein Handbook Reference)
Oxalic acid solution, 0.5 M
Oxalic acid, AR, >=99%
Oxalic acid, LR, >=98%
CHEMBL146755
DTXSID0025816
Oxalic acid solution, 0.05 M
Oxalic acid, analytical standard
BDBM14674
bis(5-azaspiro[2.5]octan-8-ol)
HY-Y0262
NSC62774
Oxalicacid,0.1NStandardizedSolution
STR01359
ZINC6021239
Tox21_202122
Tox21_303346
BBL003000
bis((2R)-azetidine-2-carbonitrile)
NSC-62774
s9354
STK379550
AKOS005449445
Oxalic acid, 5% w/v aqueous solution
CCG-266020
DB03902
MCULE-6647815245
SB40938
SB40959
SB40985
Oxalic acid, 10% w/v aqueous solution
Oxalic acid, ReagentPlus(R), >=99%
NCGC00249170-01
NCGC00257376-01
NCGC00259671-01
BP-21133
H158
Oxalic acid 10 microg/mL in Acetonitrile
Oxalic acid, 0.1N Standardized Solution
Oxalic acid, SAJ first grade, >=97.0%
bis(1-(3-methyloxetan-3-yl)ethan-1-amine)
CS-0013716
FT-0657506
Oxalic acid, Vetec(TM) reagent grade, 98%
Oxalic acid, purum, anhydrous, >=97.0% (RT)
Q184832
J-007978
F1B1B2D7-C290-4CE6-8550-F25B202AFADE
F2191-0257
Oxalic acid, puriss. p.a., anhydrous, >=99.0% (RT)
Oxalic acid, purified grade, 99.999% trace metals basis
Oxalate standard for IC, 1.000 g/L in H2O, analytical standard
Oxalic acid concentrate, 0.1 M (COOH)2 (0.2N)
Oxalic acidACIDO OSSALICO (s)
Acide oxaliqueAcide(S)
Oxalique(S)
Acido OssalicoAcido
Oxalico
Aktisal
Anhydrous Oxalic Acid
AquisalÁCido(S)
OxáLico(S)
Ethanedioate
Ethanedioic Acid
Ethanedioic acid, conjugate acid (1:2)
Ethanedionic acid
Ethandisaeure
Ethane-1,2-dioic acid
Ethanedioic acid
H2Ox
HOOCCOOH
Oxalsaeure
Ethane-1,2-dioate
Ethanedioate
Oxalate
Ammonium oxalate
Ethanedioic acid dihydrate
Ethanedionate
Ethanedionic acid
Kyselina stavelova
Oxaalzuur HMDB
Oxalic acid 2-hydrate
Oxalic acid anhydrous
Oxalic acid diammonium salt
Oxalic acid dihydrate
Acid, oxalic
Aluminum oxalate
Chromium (3+) oxalate (3:2)
Dipotassium oxalate
Iron oxalate
Magnesium oxalate
Magnesium oxalate (1:1)
Oxalate, dilithium
Oxalate, disodium
Oxalate, monohydrogen monopotassium
Oxalate, monopotassium
Oxalate, potassium
Chromium oxalate
Dilithium oxalate
Manganese (2+) oxalate (1:1)
Monosodium oxalate
Oxalate, chromium
Oxalate, dipotassium
Oxalate, magnesium
Oxalate, monosodium
Oxalate, potassium chromium
Oxalate, sodium HMDB
Potassium oxalate
Potassium oxalate (2:1)
Diammonium oxalate
Disodium oxalate
Oxalate, aluminum
Oxalate, diammonium
Oxalate, ferric
Oxalate, monoammonium
Potassium chromium oxalate
Chromium (2+) oxalate
Ferric oxalate
Iron (2+) oxalate (1:1)
Iron (3+) oxalate
Monoammonium oxalate
Monohydrogen monopotassium oxalate
Monopotassium oxalate
Oxalate, iron
Sodium oxalate
Oxalic acid
Oxalic Acid Dihydrate (Technical)
Wood Bleach
Crab Acid
LS-851
MFCD00002573
NCGC00249170-01
NCGC00257376-01
NCGC00259671-01
NCI-55209
NCI-C55209
NCIOpen2_000770
NCIOpen2_001022
NCIOpen2_001042
NCIOpen2_001202
NCIOpen2_008831
NSC 62774
NSC-62774
NSC115893
NSC62774
Oksalsyre
Oxagel
oxalate
Oxalate standard for IC
Oxalate standard for IC, 1.000 g/L in H2O, analytical standard
oxalic acid
Oxalic acid (8CI)
Oxalic acid (aqueous)
OXALIC ACID [HSDB]
OXALIC ACID [INCI]
OXALIC ACID [MI]
OXALIC ACID [VANDF]
OXALIC ACID [WHO-DD]
Oxalic acid 10 microg/mL in Acetonitrile
oxalic acid 2 hydrate
Oxalic acid 2-Hydrate
Oxalic acid anhydrous
Oxalic acid diammonium salt
Oxalic Acid Dianion
Oxalic acid dihydrate ACS
Oxalic Acid Low Ash Grade
Oxalic acid, 98%
Oxalic acid, analytical standard
Oxalic acid, anhydrous
Oxalic acid, anhydrous; (Ethanedioic acid)
Oxalic acid, AR, >=99%
Oxalic acid, LR, >=98%
Oxalic acid, purified grade, 99.999% trace metals basis
Oxalic acid, puriss. p.a., anhydrous, >=99.0% (RT)
Oxalic acid, purum, anhydrous, >=97.0% (RT)
Oxalic acid, ReagentPlus(R), >=99%
Oxalic acid, SAJ first grade, >=97.0%
Oxalic acid, Vetec(TM) reagent grade, 98%
Oxalicacid
OXD
Oxiric acid
Q184832
s9354
SB40938
SB40959
SB40985
STK379550
STR01359
TETRADECANOIC-D27ACID
Tox21_202122
Tox21_303346
Ultraplast Activate S 52
UNII-9E7R5L6H31
WLN: QVVQ
Wood bleach


OXALIC ACID DIETHYL ESTER
Oxalic acid diethyl ester is a chemical intermediate used in the manufacture of API and various dyes.
Oxalic acid diethyl ester can be used as a solvent for a number of synthetic and natural resins.
Oxalic acid diethyl ester is also used as a cost effective additive based in the dye-sensitized solar cells (DSSCs).

CAS Number: 95-92-1
EC Number: 202-464-1
Chemical Formula: C2H5OOCCOOC2H5
Molar Mass: 146.14 g/mol

Diethyl oxalate, 95-92-1, Ethyl oxalate, Ethanedioic acid, diethyl ester, Diethyl ethanedioate, diethyloxalate, Oxalic acid, diethyl ester, Oxalic ether, Oxalic Acid Diethyl Ester, Diethylester kyseliny stavelove, Ethanedioic acid, 1,2-diethyl ester, Diethyl ester of oxalic acid, 860M3ZWF6J, Diethyl oxalate, 99%, diethyl ethane-1,2-dioate, Ethyl oxalate (VAN), HSDB 2131, EINECS 202-464-1, UN2525, Diethylester kyseliny stavelove [Czech], BRN 0606350, diethyl ethaneioate, Oxalic acid diethyl, diethyl ethane-dioate, oxalic acid diethylester, 1,2-diethyl ethanedioate, Diethyl oxalate, >=99%, 4-02-00-01848 (Beilstein Handbook Reference), Ethanedioic acid diethyl ester, CHEMBL3183226, Diethyl oxalate, analytical standard, Ethyl oxalate [UN2525] [Poison], MCULE-5264218494, UN 2525, CAS-95-92-1, Diethyl oxalate, purum, >=99.0% (GC), FT-0645510, 5-pentyl-5-tetrahydropyran-2-yl-imidazolidine-2,4-dione, ETHANEDIOIC ACID,DIETHYL ESTER (DIETHYLOXALATE), F1908-0115, Z940713540, AKOS BBS-00004457, Ethanedioic acid diethyl ester, ETHYL OXALATE, Diethyl oxalate, DIETHYL ETHANEDIOATE, RARECHEM AL BI 0114, OXALIC ACID DIETHYL ESTER, C2H5OCOCOOC2H5, Ceftriaxone Impurity 2, Oxalic acid diethyl ester Oxalic acid diethyl ester Oxalic acid diethyl ester, DIethlyoxalate, Ceftriaxone Impurity 5, Ceftriaxone Impurity 11, Diethyl ester of oxalic acid, Diethyl ester, oxalic acid, Diethylester kyseliny stavelove, diethylesterkyselinystavelove, dlethyloxalate, Oxalic ether, oxalicether, Diethyl oxate, Diethyl oxalate, STANDARD FOR GC, Diethyl oxalate, 99+%, DiethyloxalateForSynthesis, diethyl ethaneioate, Diethyl oxalate, 98.0% MIN, Diethyl oxalate, 99.0% MIN, Diethyloxaiate, Oxalsurediethylester, Diαthyloxalat, oxalic acid diethylester Diethyl oxalate, Diethyl oxalate pure, GKSW, Diethyl oxalate, 99% 1KG, Diethyl oxalate, 99% 2.5KG, Diethyl oxalate, 99% 25GR, Diethyl oxalate, 99% 500GR, Dithyl oxalate, Diethyl oxalate purum, >=99.0% (GC), Diethyl oxalate [for SpectrophotoMetry], Diethyl oxalat, Diethyleoxalate, Ethanedioicacid, 1,2-diethyl ester, DiethylOxalate>, DiethylOxalate[forSpectrophotometry]>, Diethyl oxalate fandachem, Diethyl oxalate (DEOX), Diethyl oxalate ISO 9001:2015 REACH, 95-92-1, Diethyl oxalate, 95-92-1, Ethyl oxalate, Ethanedioic acid, diethyl ester, Diethyl ethanedioate, diethyloxalate, Oxalic acid, diethyl ester, Oxalic ether, Oxalic Acid Diethyl Ester, NSC 8851, UNII-860M3ZWF6J, Diethylester kyseliny stavelove, MFCD00009119, Diethyl ester of oxalic acid, 860M3ZWF6J, Ethanedioic acid, 1,2-diethyl ester, Ethyl oxalate (VAN), HSDB 2131, EINECS 202-464-1, UN2525, BRN 0606350, diethyl ethaneioate, Oxalic acid diethyl, diethyl ethane-dioate, oxalic acid diethylester, 1,2-diethyl ethanedioate, C2H5OCOCOOC2H5, Diethyl oxalate, >=99%, EC 202-464-1, SCHEMBL7262, WLN: 2OVVO2, DSSTox_CID_24472, DSSTox_RID_80254, DSSTox_GSID_44472, 4-02-00-01848, CHEMBL3183226, DTXSID2044472, NSC8851, AMY37179, NSC-8851, ZINC1648270, Diethyl oxalate, analytical standard, Tox21_302109, BBL011413, STL146519, AKOS000120214, Ethyl oxalate, MCULE-5264218494, UN 2525, CAS-95-92-1, NCGC00255767-01, AS-14315BP-13324, K733, Diethyl oxalate, purum, >=99.0% (GC), FT-0645510, O0078, O0120Q904612, J-802189, Q-200981, 5-pentyl-5-tetrahydropyran-2-yl-imidazolidine-2,4-dione, ETHANEDIOIC ACID,DIETHYL ESTER (DIETHYLOXALATE), F1908-0115, Z940713540

Due to Oxalic acid diethyl ester chemical characteristic, Oxalic acid diethyl ester (DEOX) is miscible with alcohols, ether and other common organic solvents.
Oxalic acid diethyl ester is slightly soluble in water.
Oxalic acid diethyl ester is a Diester of ethyl alcohol and oxalic acid.

Oxalic acid diethyl ester appears as a colorless liquid.
Oxalic acid diethyl ester is slightly denser than water and insoluble in water.

Oxalic acid diethyl ester undergoes transesterification with phenol in the liquid phase over very efficient MoO3/TiO2 solid-acid sol-gel catalysts to form diphenyl oxalate.
Oxalic acid diethyl ester undergoes Claisen condensation with active methylene group of ketosteroids to form glyoxalyl derivatives.
Oxalic acid diethyl ester undergoes hydrogenation in the presence of high copper contented mesoporous Cu/SBA-15 catalysts to yield ethylene glycol.

Form of Oxalic acid diethyl ester is liquid.
A sustainable process based on carbon monoxide (CO) coupling reaction has been considered as an alternative method for DEO

Oxalic acid diethyl ester appears as a colorless liquid.
Oxalic acid diethyl ester is slightly soluble in water.

Oxalic acid diethyl ester is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 tonnes per annum.
Oxalic acid diethyl ester is used in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.

Oxalic acid diethyl ester is a chemical intermediate used in the manufacture of API and various dyes.
Oxalic acid diethyl ester can be used as a solvent for a number of synthetic and natural resins.
Oxalic acid diethyl ester is also used as a cost effective additive based in the dye-sensitized solar cells (DSSCs)

Oxalic acid diethyl ester may have a promising industrial application for coal to ethylene glycol production.
Oxalic acid diethyl ester is a clear colorless liquid with characteristic.

Ethyl oxalyl Chloride is manufactured by hydrolysis of Oxalic acid diethyl ester with Potassium Carbonate.
Oxalic acid diethyl ester is a chemical used to pre-treat wood chips in order to refine and prepare them for further processing (such as obtaining wood pulp).

Oxalic acid diethyl ester is also used as a starting material to synthesize Ethylene glycol (E890140) by means of catalytic hydrogenation.
Oxalic acid diethyl ester is a chemical intermediate used in the manufacture of API and various dyes.

Applications of Oxalic acid diethyl ester:
Oxalic acid diethyl ester is used to prepare active pharmaceutical ingredients (API), plastics and dyestuff intermediates.
Oxalic acid diethyl ester is also used as a solvent for cellulose esters, ethers, resins, perfumes and lacquers for electronics.

Oxalic acid diethyl ester is involved in the transesterification reaction with phenol to get dipheny oxalate.
Oxalic acid diethyl ester is also involved in the Claisen condensation ketosteroids to prepare glyoxalyl derivatives.

Further, Oxalic acid diethyl ester is used to prepare sym-1,4-diphenyl-1,4-dihydro-1,2,4,5-polytetrazine.
In addition to this, Oxalic acid diethyl ester is utilized in the microemulsion synthesis of zinc oxide nanoparticles.

Oxalic acid diethyl ester was used in microemulsion synthesis of ZnO nanoparticles.

Uses of Oxalic acid diethyl ester:
Oxalic acid diethyl ester is used especially for production of pesticides and also as a starting material of so-called oxalate syntheses used in many areas, such as in pharmaceutical industry (production of steroids, barbiturates), in dyeing industry (Tartrazin dyestuff) and other specialised chemicals and in PU and plastic industry.

Oxalic acid diethyl ester is used to make pharmaceuticals, plastics, dyes, and dyestuff intermediates.
Oxalic acid diethyl ester is also used as a solvent for cellulose esters, ethers, resins, perfumes, and lacquers for electronics.

Oxalic acid diethyl ester is a chemical used to pre-treat wood chips in order to refine and prepare them for further processing (such as obtaining wood pulp).
Oxalic acid diethyl ester is also used as a starting material to synthesize Ethylene glycol (E890140) by means of catalytic hydrogenation.

Oxalic acid diethyl ester uses and applications include:
Solvent for cellulose esters and ethers, many natural and synthetic resins, paint stripping;
radio-tube cathode fixing lacquers;
perfumes;
chelating agent;
cleaner for polymeric residues;
pigment dispersant;
intermediate for organic synthesis, pharmaceuticals, barbiturates (CNS depressants), dyes;
in food packaging adhesives
Suggested storage of Oxalic acid diethyl ester:
Moisture-sensitive

Use and Manufacturing:
Manufacture of phenobarbital,
Ethylbenzyl malonate,
Triethylamine, & similar chemicals;
Manufacture of plastics,
Dyestuff intermediates;
Solvent for cellulose esters
Organic syntheses,
Esp in mfr of pharmaceuticals;
Solvent for ethers & resins
Olvent for perfumes & for natural & synthetic resins (cellulose esters);
Agent in radio tube cathode fixing lacquers; c
Hem int for pharmaceuticals,
Plastics & dyes.

Widespread uses by professional workers:
Oxalic acid diethyl ester is used in the following products: laboratory chemicals and polymers.
Oxalic acid diethyl ester is used in the following areas: building & construction work.
Other release to the environment of Oxalic acid diethyl ester is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).

Uses at industrial sites:
Oxalic acid diethyl ester is used in the following products: polymers and laboratory chemicals.
Oxalic acid diethyl ester has an industrial use resulting in manufacture of another substance (use of intermediates).

Oxalic acid diethyl ester is used in the following areas: building & construction work, formulation of mixtures and/or re-packaging and scientific research and development.
Oxalic acid diethyl ester is used for the manufacture of: chemicals.
Release to the environment of Oxalic acid diethyl ester can occur from industrial use: in the production of articles, for thermoplastic manufacture, of substances in closed systems with minimal release and as an intermediate step in further manufacturing of another substance (use of intermediates).

Other Industry Uses:
Intermediates
Processing aids, not otherwise listed
Agro chemical pesticide

Consumer Uses:
Apparel and footwear care products
Agro chemical pesticide

Other Uses:

Chelating:
Reacts and forms complexes with metal ions that could affect the stability and / or appearance of cosmetic products.

Hair conditioner:
Leaves hair easy to comb, soft, soft and shiny and / or confers volume, lightness and shine.

Masking:
Reduces or inhibits the odor or basic taste of the product.

Plasticiser:
Softens and softens another substance that otherwise could not easily be deformed, dispersed or worked.

Solvent:
Dissolves other substances.

Potential Uses:
Chelating agents, hair conditioning, plasticisers, solvents
Oxalic acid diethyl ester is used as a solvent for paint stripping and resins.

Oxalic acid diethyl ester is used as cleaner for polymeric residues.
Oxalic acid diethyl ester is used as pigment dispersant.
There are some specialty application of Oxalic acid diethyl ester as a solvent in nitrocellulose lacquers.

Oxalic acid diethyl ester is a chemical intermediate used in the manufacture of API and various dyes.
Oxalic acid diethyl ester can be used as a solvent for a number of synthetic and natural resins.
Oxalic acid diethyl ester is also used as a cost effective additive based in the dye-sensitized solar cells (DSSCs).

Oxalic acid diethyl ester is an important intermediate in chemical industry, especially in pharmaceutical industry, which can be utilized for the synthesis of high value drugs, dyestuff and as the useful solvent for spices.
Oxalic acid diethyl ester is used in microemulsion synthesis of ZnO nanoparticles.

Oxalic acid diethyl ester is used in the synthesis of sym-1,4-diphenyl-1,4-dihydro-1,2,4,5-polytetrazine.
Oxalic acid diethyl ester can be used in Pharma & Life Science, Agriculture, Plastics, Cosmetics & Personal Care.
Oxalic acid diethyl ester can be applied as Agrochemicals.

Oxalic acid diethyl ester is widely used in fine chemical industry.
Oxalic acid diethyl ester can be added to unmodified vegetable oils in any ratio.

As heating oil, use can be made of a mixture which, as main component, consists of vegetable oils and up to 50% by volume Oxalic acid diethyl ester.
Oxalic acid diethyl ester is used as a solvent for plastics and in the manufacture of perfumes and pharmaceuticals.

As heating oil use can be made of a mixture which originates from the refining of crude oil and is admixed with up to 25% by volume Oxalic acid diethyl ester.
Oxalic acid diethyl ester is widely utilized at industrial domains to synthesize a variety of significant fine chemicals, such as dyes, pharmaceuticals, solvents, extractants, various intermediates and ethylene glycol (EG).

Oxalic acid diethyl ester is necessary to dissolve DMO in anhydrous methanol or heat DMO to liquid state when Oxalic acid diethyl ester is applied to the production of ethylene glycol.
Oxalic acid diethyl ester is a liquid chemical at room temperature and convenient as raw material for the production of ethylene glycol by hydrogenation.

Benefits of Oxalic acid diethyl ester:
Highly efficient
Highly stable
Contributes to sustainable ethylene glycol production

General Manufacturing Information of Oxalic acid diethyl ester:
Industry Processing Sectors
All other basic organic chemical manufacturing
Pesticide, fertilizer, and other agricultural chemical manufacturing
Plastic material and resin manufacturing

Solubility of Oxalic acid diethyl ester:
Miscible with alcohols, ether and other common organic solvents.
Completely sol ether, alcohol and acetone; slightly sol hot water.

The solubility of dimethyl oxalate is similar, except that Oxalic acid diethyl ester is more soluble in water.
The solubilities of the other esters are similar in organic solvents, but they are insoluble in water.

Production of Oxalic acid diethyl ester:

Dimethyl oxalate can be obtained by esterification of oxalic acid with methanol using sulfuric acid as a catalyst:
2CH3OH+(CO2H)2 → (CO2CH3)2+2H2O

Oxidative carbonylation route:

The preparation by oxidative carbonylation has attracted interest because Oxalic acid diethyl ester requires only C1 precursors:
4CH3OH+4 CO+O2→ 2 (CO2CH3)2+2H2O

The reaction is catalyzed by Pd2+.
The synthesis gas is mostly obtained from coal or biomass.

The oxidation proceeds via dinitrogen trioxide, which is formed according to (1) of nitrogen monoxide and oxygen and then reacts according to (2) with methanol forming methyl nitrite.

In the next step of dicarbonylation (3) carbon monoxide reacts with methyl nitrite to dimethyl oxalate in the vapor phase at atmospheric pressure and temperatures at 80-120 °C over a palladium catalyst.

This method is lossless with respect to methyl nitrite, which acts practically as a carrier of oxidation equivalents.
However, the water formed must be removed to prevent hydrolysis of the dimethyl oxalate product.
With 1% Pd/α-Al2O3 dimethyl oxalate is produced selectively in a dicarbonylation reaction, under the same conditions with 2% Pd/C dimethyl carbonate is produced by monocarbonylation.

Alternatively, the oxidative carbonylation of methanol can be carried out with high yield and selectivity with 1,4-benzoquinone as an oxidant in the system Pd(OAc)2/PPh3/benzoquinone with mass ratio 1/3/100 at 65 °C and 70 atm CO.

Production Methods of Oxalic acid diethyl ester:
Oxalic acid diethyl ester is produced via esterification of ethanol and oxalic acid.
Oxalic acid diethyl esteris a preferred solvent for cellulose acetate and nitrate.

Due to Oxalic acid diethyl ester's chemical characteristic, Oxalic acid diethyl ester is miscible with alcohols, ether and other common organic solvents.

Reactions of Oxalic acid diethyl ester:
Dimethyl oxalate (and the related diethyl ester) is used in diverse condensation reactions.
For example, Oxalic acid diethyl ester condenses with cyclohexanone to give the diketo-ester, a precursor to pimelic acid.
With diamines, the diesters of oxalic acid condense to give cyclic diamides.

Quinoxalinedione is produced by condensation of dimethyloxalate and o-phenylenediamine:
C2O2(OMe)2 + C6H4(NH2)2 → C6H4(NHCO)2 + 2 MeOH

Hydrogenation gives ethylene glycol.
Dimethyl oxalate can be converted into ethylene glycol in high yields (94.7%).

The methanol formed is recycled in the process of oxidative carbonylation.
Other plants with a total annual capacity of more than 1 million tons of ethylene glycol per year are planned.

Decarbonylation gives dimethyl carbonate.

Diphenyl oxalate is obtained by transesterification with phenol in the presence of titanium catalysts, which is again decarbonylated to diphenyl carbonate in the liquid or gas phase.

Dimethyl oxalate can also be used as a methylating agent.
Oxalic acid diethyl ester is notably less toxic than other methylating agents such as methyl iodide or dimethyl sulfate.

Handling and Storage of Oxalic acid diethyl ester:

Precautions for safe handling:

Hygiene measures:
Immediately change contaminated clothing.
Apply preventive skin protection.
Wash hands and face after working with substance.

Conditions for safe storage, including any incompatibilities:

Storage conditions:
Tightly closed.
Keep in a well-ventilated place.
Keep locked up or in an area accessible only to qualified or authorized persons.

Stability and Reactivity of Oxalic acid diethyl ester:
Oxalic acid diethyl ester is an ester.
Esters react with acids to liberate heat along with alcohols and acids.

Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products.
Heat is also generated by the interaction of esters with caustic solutions.
Flammable hydrogen is generated by mixing esters with alkali metals and hydrides

Chemical stability:
Oxalic acid diethyl ester is chemically stable under standard ambient conditions (room temperature).

First Aid Measures of Oxalic acid diethyl ester:

General advice:
First aider needs to protect himself.

If inhaled:
Fresh air.
Call in physician.

In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Call a physician immediately.

In case of eye contact:
Rinse out with plenty of water.
Remove contact lenses.

If swallowed:
Make victim drink water.

Accidental Release Measures of Oxalic acid diethyl ester:

Environmental precautions:
Do not let product enter drains.

Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.

Take up carefully with liquid-absorbent material.
Dispose of properly.
Clean up affected area.

Fire Fighting Measures of Oxalic acid diethyl ester:

Extinguishing media:

Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder

Unsuitable extinguishing media:
For Oxalic acid diethyl ester no limitations of extinguishing agents are given.

Further information:
Remove container from danger zone and cool with water.
Prevent fire extinguishing water from contaminating surface water or the ground water system.

Exposure Controls/personal Protection of Oxalic acid diethyl ester:

Eye/face protection:
Use tightly fitting safety goggles.

Skin protection:
Full contact

Material: butyl-rubber
Minimum layer thickness: 0,7 mm
Break through time: 480 min

Splash contact:

Material: Nitrile rubber
Minimum layer thickness: 0,4 mm
Break through time: 10 min

Body Protection:
protective clothing

Control of environmental exposure:
Do not let product enter drains.

Identifiers of Oxalic acid diethyl ester:
CAS Number: 553-90-2
ChemSpider: 10649
ECHA InfoCard: 100.008.231
PubChem CID: 11120
UNII: IQ3Q79344S
CompTox Dashboard (EPA): DTXSID9060287
InChIInChI=1S/C4H6O4/c1-7-3(5)4(6)8-2/h1-2H3
Key: LOMVENUNSWAXEN-UHFFFAOYSA-N
InChI=1/C4H6O4/c1-7-3(5)4(6)8-2/h1-2H3
Key: LOMVENUNSWAXEN-UHFFFAOYAF
SMILES: O=C(OC)C(=O)OC

INCI name: Oxalic acid diethyl ester
EINECS/ELINCS number: 202-464-1
Classification: Regulated
Restriction in Europe: III/3

EC / List no.: 202-464-1
CAS no.: 95-92-1
Mol. formula: C6H10O4

CAS number: 95-92-1
EC index number: 607-147-00-5
EC number: 202-464-1
Hill Formula: C₆H₁₀O₄
Chemical formula: C₂H₅OOCCOOC₂H₅
Molar Mass: 146.14 g/mol
HS Code: 2917 11 00

Synonym(s): Diethyl ethanedioate, Ethyl oxalate
Linear Formula: C2H5OCOCOOC2H5
CAS Number: 95-92-1
Molecular Weight: 146.14
Beilstein: 606350
EC Number: 202-464-1
MDL number:MFCD00009119
PubChem Substance ID:24848078
NACRES:NA.22

Properties of Oxalic acid diethyl ester:
Physical State: Liquid
Storage: Store at room temperature
Melting Point: -41° C (lit.)
Boiling Point: 185° C (lit.)
Density: 1.08 g/cm3 at 25° C

Formula: C6H10O4
Formula Weight: 146.14
Melting point: -41°
Boiling Point: 184-186°
Flash Point: 75°(167°F)
Density: 1.077
Refractive Index: 1.4100
Storage & Sensitivity:
Moisture Sensitive.
Store under Argon.
Ambient temperatures.
Solubility:
Miscible with alcohols, ether and other common organic solvents.

Molecular Weight: 146.14
XLogP3: 0.6
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 5
Exact Mass: 146.05790880
Monoisotopic Mass: 146.05790880
Topological Polar Surface Area: 52.6 Ų
Heavy Atom Count: 10
Complexity: 114
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Assay as Deo by G.C.: 98% Min.
Acidity as Oxalic Acid: 0.10% Max.
Moisture Contents: 0.105 Max.
Relative Density: 1.078 - 1.082
Boiling Range: 181 - 188°C

Appearance: colorless clear liquid (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity: 1.07600 to 1.08200 @ 25.00 °C.
Pounds per Gallon - (est).: 8.953 to 9.003
Refractive Index: 1.40700 to 1.41300 @ 20.00 °C.

Melting Point: -41.00 to -40.00 °C. @ 760.00 mm Hg
Boiling Point: 185.70 °C. @ 760.00 mm Hg
Boiling Point: 113.00 to 114.00 °C. @ 50.00 mm Hg
Vapor Pressure: 0.414000 mmHg @ 25.00 °C.
Vapor Density: 5.03 ( Air = 1 )
Flash Point: 168.00 °F. TCC ( 75.56 °C. )
logP (o/w): 0.560

Appearance Form: liquid
Color: colorless
Odor: aromatic
Odor Threshold: 0,1 ppm
pH: No data available
Melting point/range: -41 °C - lit.
Initial boiling point and boiling range: 185 °C - lit.
Flash point 75 °C - closed cup

Upper explosion limit: 2,67 %(V)
Lower explosion limit: 0,42 %(V)
Vapor pressure 1,33 hPa at 47 °C
Vapor density 5,04 - (Air = 1.0)

Relative density 1,08 at 20 °C
Water solubility at 20 °C
Partition coefficient: n-octanol/water log Pow: 0,56 - (Lit.)
Autoignition temperature: 412 °C at 984 hPa
Decomposition temperature: Distillable in an undecomposed state at normal pressure.
Viscosity Viscosity, kinematic: No data available
Viscosity, dynamic: 2,01 mPa.s at 20 °C

Specifications of Oxalic acid diethyl ester:
Assay (GC, area%): ≥ 98.0 % (a/a)
Density (d 20 °C/ 4 °C): 1.076 - 1.079
Identity (IR): passes test

Names of Oxalic acid diethyl ester:

Regulatory process names:
Diethyl ethanedioate
Diethyl oxalate
Diethyl oxalate
diethyl oxalate
Diethylester kyseliny stavelove
Ethanedioic acid, 1,2-diethyl ester
Ethanedioic acid, diethyl ester
ETHYL OXALATE
Ethyl oxalate
Ethyl oxalate (VAN)
oxalic acid diethylester diethyl oxalate
oxalic acid diethylester; diethyl oxalate
Oxalic acid, diethyl ester
Oxalic ether

Translated names:
acid oxalic dietilester dietil oxalat (ro)
diethylester čťavelové kyseliny diethyl-oxalát (cs)
diethyloxalaat (nl)
diethyloxalat ethyloxalat (da)
Diethyloxalat Oxalsäurediethylester (de)
dietil ester oksalne kisline dietil oksalat (sl)
dietile ossalato etile ossalato (it)
dietylester kyseliny šťaveľovej dietyl-oxalát (sk)
dietyloksalat etyloksalat (no)
dietyloxalat (sv)
Dietyylioksalaatti (fi)
diéthylester de l'acide oxalique; oxalate de diéthyle oxalate d'éthyle (fr)
Oksaalhappe dietüülester Dietüüloksalaat (et)
oksalo rūgšties dietilesteris dietiloksalatas (lt)
oxalato de dietilo oxalato de etilo (pt)
oxalato de dietilo éster dietílico del ácido oxálico (es)
oxálsav-dietil-észter dietil-oxalát (hu)
skābeņskābes dietilesteris dietiloksalāts (lv)
szczawian dietylu ester dietylowy kwasu szczawiowego (pl)
οξαλικός διαιθυλεστέρας (el)
диетилов естер на оксаловата киселина диетил оксалат (bg)

IUPAC names:
DIETHYL OXALATE
Diethyl Oxalate
Diethyl oxalate
diethyl oxalate
Diethyl oxalate
diethyl oxalate
diethylester
Diethyloxalat
Oxalic acid diethylester
oxalic acid diethylester

Trade names:
BRUGGOLEN P22

Other identifiers:
607-147-00-5
95-92-1
OXALİC ACID
Molecular Formula: C2H2O4 or (COOH)2 or HOOCCOOH
Molecular Weight: 90.03
CAS No: 144-62-7



APPLICATIONS


Oxalic acid's main applications include cleaning or bleaching, especially for the removal of rust (iron complexing agent).

Oxalic Acid's utility in rust removal agents is due to its forming a stable, water-soluble salt with ferric iron, ferrioxalate ion.
The cleaning product Zud contains oxalic acid.
Oxalic acid is an ingredient in some tooth whitening products.
About 25% of produced oxalic acid will be used as a mordant in dyeing processes.

Oxalic Acid is also used in bleaches, especially for pulpwood, and for rust removal and other cleaning, in baking powder, and as a third reagent in silica analysis instruments.

Oxalic acid is used by some beekeepers as a miticide against the parasitic varroa mite.
Thymovar combined with an oxalic acid treatment has proved effective against the varroa mite.

Oxalic acid is an odorless white solid.
Furthermore, Oxalic Acid sinks and mixes with water.

Oxalic acid is an alpha,omega-dicarboxylic acid that is ethane substituted by carboxyl groups at positions 1 and 2.
Moreover, Oxalic Acid has a role as a human metabolite, a plant metabolite and an algal metabolite.
Oxalic Acid is a conjugate acid of an oxalate(1-) and an oxalate.

Oxalic acid is a metabolite found in the aging mouse brain.
Dilute solutions (0.05–0.15 M) of oxalic acid can be used to remove iron from clays such as kaolinite to produce light-colored ceramics.
Oxalic acid is used to clean minerals.

Oxalic acid is sometimes used in the aluminum anodizing process, with or without sulfuric acid.
Compared to sulfuric acid anodizing, the coatings obtained are thinner and exhibit lower surface roughness.
Oxalic acid is also widely used as a wood bleach, most often in its crystalline form to be mixed with water to its proper dilution for use.

Oxalic acid is also used in electronic and semiconductor industries.
In 2006 Oxalic Acid was reported being used in electrochemical–mechanical planarization of copper layers in the semiconductor devices fabrication process.


Uses of Oxalic Acid:

Batteries
Cleaning and safety
Products used for cleaning or safety in an occupational or industrial setting (e.g. Cleaning products and household care)
Bathtub, tile, and toilet surface cleaners acid
Cleaning products for general household cleaning
Products that remove stains or discoloration of fabric (including color-safe bleaches) used in laundry
Disinfectant
Products used to control microbial pests on hard surfaces or laundry
Metal specific
Metal polish
Products used to polish metal surfaces
Cons. electronics, mech. appliances, and machinery
Including small and large consumer electronics appliances (e.g. refrigerator, washing machine, vacuum cleaner, computer, phone, smoke detector)
Paint/stain and related products
Stripper
Products applied to hard surfaces to remove paints and finishes
Fragrance
fragrance component
pH regulating agent
pH regulation
Raw materials
Pure chemicals or ingredients
Boat cleaner
Cleaners, washes, and polishes for cleaning marine hulls applications
Rust remover

Oxalic Acid is used in the dyeing process as a mordant
Furthermore, Oxalic Acid is used in removing rust

In lanthanide chemistry, Oxalic Acid is used as an important reagent
Oxalic Acid is applied on marble sculptures to make it shine

Oxalic Acid is used in the manufacture of dye
More to that, Oxalic Acid is used in bleaches

Oxalic Acid is used in removing food and ink stains
Moreover, Oxalic Acid is used in developing photographic film
Oxalic Acid is used in wastewater treatment to remove the calcium deposit.

Oxalic acid’s conjugate base is the hydrogen oxalate anion and its conjugate base (commonly known as oxalate) is a competitive lactate dehydrogenase (often abbreviated to LDH) enzyme inhibitor.
Further, Oxalic Acid catalyses the conversion of pyruvate to lactic acid (end product of the fermentation, which is an anaerobic process) oxidizing coenzyme NADH to NAD+ and H+ at the same time.

Restoring NAD+ levels is necessary if anaerobic energy metabolism is to continue through glycolysis.
Because cancer cells preferentially use anaerobic metabolism, Oxalic Acid inhibition has been shown to inhibit tumour development and growth.
Thus, Oxalic Acid provides an interesting possible course for the treatment of certain cancers.



DESCRIPTION


Oxalic acid is an organic acid with the systematic name ethanedioic acid and formula HO2C−CO2H.
Further, Oxalic Acid is the simplest dicarboxylic acid.
Oxalic Acid is a white crystalline solid that forms a colorless solution in water.

Name of Oxalic Acid comes from the fact that early investigators isolated oxalic acid from flowering plants of the genus Oxalis, commonly known as wood-sorrels.
Oxalic Acid occurs naturally in many foods.
Excessive ingestion of oxalic acid or prolonged skin contact can be dangerous.

Oxalic Acid is colorless, odorless powder or granular solid.
Furthermore, Oxalic Acid is found in many vegetables and plants.
Oxalic Acid is the simplest dicarboxylic acid with condensed formula HOOC-COOH and has an acidic strength greater than acetic acid.

Excess consumption of oxalic acid can be dangerous.
Oxalic Acid is produced by the oxidation of carbohydrates.

Oxalic Acid can also be prepared in the laboratory by the oxidation of sucrose in the presence of nitric acid and a catalyst like vanadium pentoxide.
Moreover, Oxalic acid has a structure with two polymorphs and it appears as a white crystalline solid which becomes a colourless solution when dissolved in water.
Oxalic Acid is a reducing agent and is used as a chelating agent with oxalate as its conjugate base.

Oxalic Acid, also called ethanedioic acid, a colourless, crystalline, toxic organic compound belonging to the family of carboxylic acids.

Oxalic acid is widely used as an acid rinse in laundries, where it is effective in removing rust and ink stains because it converts most insoluble iron compounds into a soluble complex ion.
For the same reason, Oxalic Acid is the chief constituent of many commercial preparations used for removing scale from automobile radiators.

The formula of oxalic acid is (C2H2O4).
The usual form of Oxalic Acid is that of the crystalline hydrate, (COOH)2·2H2O.
Oxalic Acid is known as a constituent of wood sorrel as early as the 17th century, oxalic acid was first prepared synthetically in 1776.

Oxalic Acid is manufactured by heating sodium formate in the presence of an alkali catalyst, by oxidizing carbohydrates with nitric acid, by heating sawdust with caustic alkalies, or by fermentation of sugar solutions in the presence of certain molds.
Moreover, Oxalic acid has much greater acid strength than acetic acid.

Oxalic Acid is a reducing agent and its conjugate base, known as oxalate (C2O2−4), is a chelating agent for metal cations.
Typically, oxalic acid occurs as the dihydrate with the formula C2H2O4·2H2O.

The preparation of salts of oxalic acid (crab acid) from plants had been known, at least since 1745, when the Dutch botanist and physician Herman Boerhaave isolated a salt from wood sorrel.
By 1773, François Pierre Savary of Fribourg, Switzerland had isolated oxalic acid from its salt in sorrel.

In 1776, Swedish chemists Carl Wilhelm Scheele and Torbern Olof Bergman produced oxalic acid by reacting sugar with concentrated nitric acid; Scheele called the acid that resulted socker-syra or såcker-syra (sugar acid).
By 1784, Scheele had shown that "sugar acid" and oxalic acid from natural sources were identical.
In 1824, the German chemist Friedrich Wöhler obtained oxalic acid by reacting cyanogen with ammonia in aqueous solution.
This experiment may represent the first synthesis of a natural product.

Oxalic acid is mainly manufactured by the oxidation of carbohydrates or glucose using nitric acid or air in the presence of vanadium pentoxide.
A variety of precursors can be used including glycolic acid and ethylene glycol.

A newer method entails oxidative carbonylation of alcohols to give the diesters of oxalic acid:
4 ROH + 4 CO + O2 → 2 (CO2R)2 + 2 H2O

These diesters are subsequently hydrolyzed to oxalic acid.
Approximately 120,000 tonnes of Oxalic Acid are produced annually.

Historically oxalic acid was obtained exclusively by using caustics, such as sodium or potassium hydroxide, on sawdust, followed by acidification of the oxalate by mineral acids, such as sulfuric acid.
Oxalic acid can also be formed by the heating of sodium formate in the presence of an alkaline catalyst.

Leafy greens, legumes, and most other plant foods contain a nutrient called oxalate or oxalic acid.
Oxalic Acid is a naturally occurring chemical you get through your diet.

The body also produces Oxalic Acid as waste.
Foods rich in Oxalic Acid also contain other nutrients that your body needs for good health.

Oxalic acid occurs naturally in many plants like the following:

Fruits
Cocoa
Leafy green vegetables
Nuts
Seeds
Spinach
Sweet potatoes
Star fruit
Turnip greens
Endive
Swiss chard
Beet greens

When oxalic acid mixes with other minerals, it forms oxalate.
People regularly use the two terms interchangeably to refer to the same thing: Oxalic Acid.

Your body produces oxalate and also gets it from food sources.
Oxalic Acid changes to oxalate when your body processes it.

Oxalic Acid is a poisonous strong acid (COOH)2 or H2C2O4 that occurs in various plants (such as spinach) as oxalates and is used especially as a bleaching or cleaning agent and as a chemical intermediate



PROPERTIES


Molecular Weight: 90.03
XLogP3-AA: -0.3
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 1
Exact Mass: 89.99530854
Monoisotopic Mass: 89.99530854
Topological Polar Surface Area: 74.6 Ų
Heavy Atom Count: 6
Formal Charge: 0
Complexity: 71.5
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes



FIRST AID


Eye Contact:

Immediately flush with large amounts of water for at least 30 minutes, lifting upper and lower lids.
Remove contact lenses, if worn, while flushing.
Seek medical attention immediately.

Skin Contact:

Quickly remove contaminated clothing.
Immediately wash contaminated skin with large amounts of soap and water.
Seek medical attention.

Inhalation:

Remove the person from exposure.
Begin rescue breathing (using universal precautions) if breathing has stopped and CPR if heart action has stopped.
Transfer promptly to a medical facility.



HANDLING AND STORAGE


Prior to working with Oxalic Acid you should be trained on its proper handling and storage.

Oxalic Acid reacts violently with OXIDIZING AGENTS (such as PERCHLORATES, PEROXIDES, PERMANGANATES,
CHLORATES, NITRATES, CHLORINE, BROMINE and FLUORINE); FURFURYL ALCOHOL; and CHLORITES to cause fires and explosions.
Oxalic Acid will react with SILVER and SILVER COMPOUNDS to form explosive Silver Oxalate.

Oxalic Acid is not compatible with STRONG ACIDS (such as HYDROCHLORIC, SULFURIC and NITRIC); STRONG BASES (such as SODIUM HYDROXIDE and POTASSIUM HYDROXIDE); ALKALI METALS (such as LITHIUM, SODIUM and POTASSIUM); and ACID CHLORIDES.
Store in tightly closed containers in a cool, well-ventilated area away from MOISTURE and COMBUSTIBLES.

Sources of ignition, such as smoking and open flames, are prohibited where Oxalic Acid is used, handled, or stored in a manner that could create a potential fire or explosion
hazard.
Oxalic Acid corrodes STEEL.



SYNONYMS


oxalic acid
ethanedioic acid
144-62-7
Aktisal
Aquisal
oxalate
Oxiric acid
Oxalsaeure
Oxaalzuur
Kyselina stavelova
Acide oxalique
Acido ossalico
Acidum oxalicum
Caswell No. 625
Oxaalzuur [Dutch]
Oxalsaeure [German]
Oxalicacid
NCI-C55209
Ethanedionic acid
Acide oxalique [French]
Ethane-1,2-dioic acid
Acido ossalico [Italian]
Kyselina stavelova [Czech]
CCRIS 1454
EPA Pesticide Chemical Code 009601
HSDB 1100
AI3-26463
NSC 62774
BRN 0385686
HOOCCOOH
Oxalic acid anhydrous
MFCD00002573
CHEBI:16995
9E7R5L6H31
C2-beta-polymorph
NSC-62774
ETHANEDIOIC ACID DIHYDRATE
Ethanedioic acid-d2
Oxalic Acid Dianion
DSSTox_CID_5816
C00209
DSSTox_RID_77935
DSSTox_GSID_25816
Oxalic acid diammonium salt
Wood bleach
Oxaliplatin Related Compound A
CAS-144-62-7
OXD
C2H2O4
NSC115893
EINECS 205-634-3
Ethandisaeure
Ethanedionate
Oxagel
UNII-9E7R5L6H31
2dua
2hwg
H2ox
Anhydrous oxalic acid
Ethane-1,2-dioate
Oxalic acid, 98%
Oxalic acid (8CI)
oxalic acid 2 hydrate
Oxalic acid, anhydrous
Oxalic acid 2-Hydrate
1o4n
1t5a
Oxalate standard for IC
WLN: QVVQ
Ethanedioic acid (9CI)
OXALIC ACID [MI]
Oxalic acid dihydrate ACS
Ultraplast Activate S 52
bmse000106
EC 205-634-3
Oxalic Acid Low Ash Grade
OXALIC ACID [HSDB]
OXALIC ACID [INCI]
NCIOpen2_000770
NCIOpen2_001022
NCIOpen2_001042
NCIOpen2_001202
NCIOpen2_008831
OXALIC ACID [VANDF]
TETRADECANOIC-D27ACID
4-02-00-01819 (Beilstein Handbook Reference)
OXALIC ACID [WHO-DD]
Oxalic acid solution, 0.5 M
Oxalic acid, AR, >=99%
Oxalic acid, LR, >=98%
CHEMBL146755
DTXSID0025816
Oxalic acid solution, 0.05 M
Oxalic acid, analytical standard
BDBM14674
bis(5-azaspiro[2.5]octan-8-ol)
HY-Y0262
NSC62774
Oxalicacid,0.1NStandardizedSolution
STR01359
ZINC6021239
Tox21_202122
Tox21_303346
BBL003000
bis((2R)-azetidine-2-carbonitrile)
s9354
STK379550
AKOS005449445
Oxalic acid, 5% w/v aqueous solution
CCG-266020
DB03902
SB40938
SB40959
SB40985
Oxalic acid, 10% w/v aqueous solution
Oxalic acid, ReagentPlus(R), >=99%
NCGC00249170-01
NCGC00257376-01
NCGC00259671-01
BP-21133
Oxalic acid 10 microg/mL in Acetonitrile
Oxalic acid, 0.1N Standardized Solution
Oxalic acid, SAJ first grade, >=97.0%
bis(1-(3-methyloxetan-3-yl)ethan-1-amine)
CS-0013716
FT-0657506
Oxalic acid, Vetec(TM) reagent grade, 98%
OXALIPLATIN IMPURITY A [EP IMPURITY]
OXALIPLATIN RELATED COMPOUND A [USP-RS]
Oxalic acid, purum, anhydrous, >=97.0% (RT)
Q184832
J-007978
OXALIPLATIN RELATED COMPOUND A [USP IMPURITY]
F1B1B2D7-C290-4CE6-8550-F25B202AFADE
Ethanedioic acid; Aktisal
Aquisal
Oxiric acid; HOOCCOOH
Acide oxalique
Acido ossalico
Ethanedionic acid
Kyselina stavelova
NCI-C55209
Oxaalzuur
Oxalsaeure
Ethane-1,2-dioic acid
NSC 62774
F2191-0257
Oxalic acid, puriss. p.a., anhydrous, >=99.0% (RT)
Oxalic acid, purified grade, 99.999% trace metals basis
Oxalate standard for IC, 1.000 g/L in H2O, analytical standard
Oxalic acid concentrate, 0.1 M (COOH)2 (0.2N), eluent concentrate for IC
OXIDIZED PE WAX
Oxidized PE Wax also known as OPE wax.
Oxidized PE Wax is an excellent new type of polar wax.


CAS Number: 68441-17-8
EC Number: 614-498-8
MDL Number: MFCD00084426
Molecular Formula: C51H102O21Si2



SYNONYMS:
Poe, Ployoxyethylene, Oxidized polyethylene, Oxidizedpolyethylene, Oxidizedpolyethylenewaxes, Ethene, homopolymer, oxidized, Polyethylene,oxidised, Oxidizedpolyethylenewax, Ethene,homopolymer,oxidized, Oxidisedpolyethylenewax, Polyethylene, oxidiz, Oxidized polyethylene wax, Poly(ethylene) oxidized, Polyethylene, oxidized, Poe, Ployoxyethylene, Oxidized polyethylene, Oxidizedpolyethylene, Oxidizedpolyethylenewaxes, Ethene, homopolymer, oxidized, Polyethylene,oxidised, Oxidizedpolyethylenewax, Ethene,homopolymer,oxidized, Oxidisedpolyethylenewax, Polyethylene, oxidiz, Oxidized polyethylene wax, Poly(ethylene) oxidized, Polyethylene, oxidized,



Oxidized PE Wax is an excellent polar wax.
Oxidized PE Wax has special properties such as low viscosity, high softening point, and hardness.
Meanwhile, Oxidized PE Wax is non-toxic, has good thermal stability, and has low volatility at high temperatures, good dispersion.


Oxidized PE Wax is an ideal product to replace Mongolian wax, sichuan wax, liquid paraffin wax, microcrystalline wax, natural paraffin wax, polyethylene wax and so on.
Oxidized PE Wax production by polyethylene wax after a special oxidation process oxidation system.


Oxidized PE Wax has low molecular weight polyethylene oxide containing hydroxyl and carboxyl groups
Oxidized PE Wax is white and slightly yellow powder, with good chemical stability, soluble in aromatic hydrocarbons
Oxidized PE Wax is made from polyethylene wax after special oxidation process.


Oxidized PE Wax has certain functional groups on the molecular chain, so its compatibility with polar resins has been significantly improved, which is better than polyethylene wax, and has good compatibility with rubber, plastics, paraffin wax and other materials.
Oxidized PE Wax can improve the dispersity of colorant, give products a good luster and improve production efficiency.


Oxidized PE Wax has good internal and external lubricity, thus it can achieve better lubricating property than the other lubricants when it’s used in the formula of rigid transparent or opaque PVC products.
Oxidized PE Wax is a type of polyethylene wax that has undergone an oxidation process.


Oxidized PE Wax is derived from the polymerization of ethylene gas and is commonly used in various industries due to its unique properties.
Oxidized PE Wax can improve the production efficiency of plastic processing and reduce the production cost.
Oxidized PE Wax also known as OPE wax.


Oxidized PE Wax is a water-soluble and thermoplastic non-ionic linear macromolecule polymer, which has the properties of flocculation, thickening, slow release, lubrication, dispersion, retention, water retention, etc., and is non-toxic and non-irritating.
Oxidized PE Wax is a low molecular weight polyethylene with hydroxyl and carboxyl.


Oxidized PE Wax acts as a lubricant. Offers good chemical durability.
Oxidized PE Wax is an excellent new type of polar wax.
Oxidized PE Wax has special properties such as low viscosity, high softening point and good hardness.


Oxidized PE Wax has excellent internal and external lubrication.
Oxidized PE Wax has good cold resistance, heat resistance, chemical resistance and wear resistance, and has good compatibility with polyethylene, polypropylene, polyvinyl acetate, and butyl rubber.


Oxidized PE Wax is an indispensable chemical material that can be used in wide range of industries and have various applications.
Low production cost, good compatibility with polyolefin resin, Oxidized PE Wax has good moisture resistance at room temperature, strong chemical resistance, excellent electrical properties, can improve the appearance of finished products.


The molecular chain has certain functional groups, so Oxidized PE Wax's miscibility with polar resin has been significantly improved.
Due to a certain amount of carbonyl and hydroxyl groups in the molecular chain of Oxidized PE Wax, the compatibility with fillers, pigments and polar resins is significantly improved.


The wettability and dispersibility in polar system are better than that of polyethylene wax, and Oxidized PE Wax also has coupling property.
Oxidized PE Wax is in the plastic processing industry, the internal and external lubrication of PVC is relatively balanced.
The lubricity of Oxidized PE Wax added to the rigid, transparent and opaque PVC formula is better than that of other lubricants.


Oxidized PE Wax molecules have polar groups like carbonyl groups and hydroxyl groups, a property which increases the compatibility with fillers, pigments, and polar resins.
Wettability and dispersibility of Oxidized PE Wax are also better than polyethylene wax.


Oxidized PE Wax is a low adhesive and hard polymer which has good chemical and heat stability, high softening point and also good lubricant effect.
The molecular chain of Oxidized PE Wax has certain functional groups, so its solubility with polar resin has been significantly improved, which is superior to polyethylene wax.


Low density Oxidized PE Wax can be plasticized ahead of time, and the later torque is reduced.
Oxidized PE Wax has no toxicity, good thermal stability, low volatility at high temperature, excellent dispersibility to fillers and pigments, excellent external lubricity and Strong internal lubrication, but also coupled.


Oxidized PE Wax's performance is comparable to the US Honeywell AC wax.
Oxidized PE Wax can improve the production efficiency of plastic processing, reduce the production cost, has good compatibility with polyolefin resin, etc.
Oxidized PE Wax can improve the fluidity of polyethylene, polypropylene, ABS and the demoulding of polymethyl methacrylate and polycarbonate.


For PVC and other external lubricants, Oxidized PE Wax has stronger internal lubricating effect compared with other external lubricants.
Oxidized PE Wax has low viscosity, high softening point, hardness.
Oxidized PE Wax can improve the fluidity of polyethylene, polypropylene and ABS and the demoulding property of polymethylmethacrylate and polycarbonate.


Oxidized PE Wax has good special performance, such as non-toxicity, good thermal stability, high temperature and low volatility, excellent dispersity of fillers, pigments, both excellent external lubricity, and strong internal lubrication.
Oxidized PE Wax also has coupling effect, can improve the production efficiency of plastic processing.


Due to its high melting point and low viscosity, Oxidized PE Wax promotes good resin fluidity, relatively reduces the power consumption of resin mixing, reduces the adhesion between resin and mold, is easy to remove film, plays the role of internal and external lubrication, and has good antistatic property.


Oxidized PE Wax has good moisture resistance at normal temperature, strong chemical resistance, excellent electrical properties, and can improve the appearance of finished products.


Oxidized PE Wax can replace the products of Mengdan wax, Sichuan wax, liquid paraffin, microcrystalline paraffin, natural paraffin, and polyethylene wax, etc, and its performance is comparable to that of the Honeywell A-C wax.
Oxidized PE Wax is a versatile material known for its applications in various industries.


Oxidized PE Wax is a type of polyethylene wax that has undergone an oxidation process.
Oxidized PE Wax has excellent internal and external lubrication.
Oxidized PE Wax is obtained by oxidation of polyethylene wax.


PE wax is non-oxidized wax, OPE wax is oxidized wax, with a certain acid value, oxidized wax molecular chain with a certain amount of carbonyl and hydroxyl, Oxidized PE Wax is excellent new polar wax, so the compatibility with fillers, pigments, polar resins is significantly improved, lubricity, dispersion is better than polyethylene wax, but also both coupling properties.


However, when subjected to an oxidation process, the properties of PE wax are enhanced, resulting in a valuable product called Oxidized PE Wax.
Oxidized PE Wax can improve the fluidity of polyethylene, polypropylene and ABS and the demoulding property of polymethylmethacrylate and polycarbonate.
Oxidized PE Wax proves to be a true chameleon in the world of industrial applications, with its versatility and adaptability to various industries.



USES and APPLICATIONS of OXIDIZED PE WAX:
Oxidized PE Wax is used as processing auxiliaries for PVC shapes, pipes and plates to increase the surface smoothness.
Oxidized PE Wax offers very good internal and external lubrication performance.
Oxidized PE Wax is used in many products, such as PVC compound, PVC profile, PVC pipe, PVC cable filler, TPE processing aids, hot melt adhesives, and PVC sheet.


Oxidized PE Wax acts as the lubricant, cost-saving agent and release agent in the course of extruding, calendaring, injecting, blowing molding of PE, PP and other plastic.
Oxidized PE Wax is applied in the field of hot melt road marking material.


Oxidized PE Wax is used in colour masterbatch, polypropylene masterbatch, additives masterbatch, Filling masterbatch and other pigment or filler: Dispersant, lubricant, brightener, coupling agent.
Oxidized PE Wax is used in rubber: processing lubricant, remover and solvent.


Oxidized PE Wax is used in ink: dispersant , anti liniment.
Oxidized PE Wax is used in Hot melt adhesive: Viscosity regulator.
Oxidized PE Wax is used in Aluminum foil composite paper: processing aids.


Oxidized PE Wax is used as Flooring coatings, leather coating, shoe polish, wax polish, car wax, wax rod, ink, cosmetics, match wear-resisting agent, ceramics, precision casting agent, oil absorbent, sealant, medicine, hot melt adhesive, Lawan paint and powder coating matting agent, cable material additives, wax, wax oil suction pen, carbon paper, wax paper, inkpad, photosensitive material matrix, textile softener, electronic component sealant, transistor agent, packet rubber processing aid, car bottom oil, dental materials, processing aids, steel rust etc..


Oxidized PE Wax is suitable for all kinds of natural fiber content, cotton, polyester/cotton fabric, chemical fiber wool-like fabric post-processing, especially suitable for Cotton, polyester/cotton of hydrophilic soft finishing, polyester prevent hair and other wool fabric after treatment.
Oxidized PE Wax is very suitable for wood-plastic composite materials, profiles, masterbatch, rubber materials and other fields.


Oxidized PE Wax can be used as PVC and other plastic lubricant.
Oxidized PE Wax is used in many products, such as PVC compound, PVC profile, PVC pipe, PVC cable filler, TPE processing aids, hot melt adhesives, and PVC sheet.


Oxidized PE Wax acts as the lubricant, cost-saving agent and release agent in the course of extruding, calendering, injecting, blowing molding of PE, PP and other plastic.
Oxidized PE Wax acts as the dispersant for masterbatches, pigment, carbon black, additive for parent material, filling parent material and other pigments.


Oxidized PE Wax is applied in the field of hot melt road marking material.
Oxidized PE Wax acts as the additive for shoeshine, floor wax, car wax, polishing wax, chinaware, pill wax, paint, coating, cable, carbon paper, wax paper, textile softening agent etc.


Oxidized PE Wax is used excellent internal and external lubrication.
Oxidized PE Wax can improve the lubricity between polymer and metal.
Oxidized PE Wax can improve the dispersion of colorants.


Oxidized PE Wax is used give products good transparency and luster.
Oxidized PE Wax is used better improve production efficiency.
Oxidized PE Wax is used Stabilizer, Modified asphalt, Wax emulsion, and PVC products.


Oxidized PE Wax is used in various industries to solve a wide range of tasks.
Oxidized PE Wax is also widely applied to PE or PVC cables, PVC profiles, pipe as new-type plastic lubricants.
Oxidized PE Wax is made from polyethylene wax by special oxidation process.


Oxidized PE Wax is a non-toxic, good thermal stability, low temperature volatility, excellent dispersion for fillers and pigments.
Oxidized PE Wax not only has excellent external lubricity, but also has a strong internal lubricating effect, and also has a coupling effect, which can improve the production efficiency of plastic processing and reduce production costs.


Oxidized PE Wax is used coating Auxiliary Agents, Electronics Chemicals, Leather Auxiliary Agents, Paper Chemicals, Petroleum Additives, Plastic Auxiliary Agents, Rubber Auxiliary Agents, Surfactants, Textile Auxiliary Agents.
Oxidized PE Wax has special properties such as low viscosity, high softening point and good hardness.


Oxidized PE Wax is used in many products, such as PVC compound, PVC profile, PVC pipe, PVC cable filler, TPE processing aids, hot melt adhesives, and PVC sheet.
Oxidized PE Wax is widely used in papermaking, coatings, inks, textile printing and dyeing, daily chemical industries and other industries.


Oxidized PE Wax used in color masterbatch, PVC products, Wax emulsion (emulsification) , modified material.
Oxidized PE Wax is used as lubricants in the processing of plastics , used in the field of hot melt road marking material, act as dispersant for masterbatches, pigment, carbon black, can be used as additive for various types of waxes like shoeshine, floor wax, car wax etc.


Oxidized PE Wax can also be used as raw and auxiliary materials for textile softener, car wax and leather softener.
Oxidized PE Wax can be used as dispersant, lubricant, brightener and coupling agent of pigment or filler such as dense masterbatch, polypropylene masterbatch, additive masterbatch and filling masterbatch.


Oxidized PE Wax is used rubber and plastic processing lubricants, film removers and phase solvents.
In the formulation of waterborne coatings and inks, Oxidized PE Wax provides excellent wear resistance, adhesion resistance and scratch resistance.
At present, Oxidized PE Wax is widely used in PVC foam board, but it is less used in other aspects due to price reasons.


PVC foam board is the most difficult to produce in PVC products, which has the most problems and is the most difficult to solve.
The plasticization can be significantly accelerated after adding oxidized.
Oxidized PE Wax is widely used in water-based coatings and ink formulations to provide excellent abrasion resistance, anti-adhesion and scratch resistance.


Oxidized PE Wax can also be used to make raw and auxiliary materials for textile softener, car wax, and leather softener.
Oxidized PE Wax is made from polyethylene wax by special oxidation process.
Oxidized PE Wax has special properties such as low viscosity, high softening point and good hardness.


Oxidized PE Wax is non-toxic, has good thermal stability, low temperature volatility, and excellent dispersion for fillers and pigments.
Oxidized PE Wax can also be emulsified in water. Emulsions are used in finishing of textiles to get a smooth surface which facilitates further production steps.


The additive for rubber process and car anti-rust agent etc.
A method of preparation of Oxidized PE Wax, which has many applications such as in plastics, rubber, leather, paper, inks and textiles, etc. was developed.
Polyethylene waxes provide stronger internal lubrication for PVC than other external lubricants.


Oxidized PE Wax is used as lubricants in the processing of plastics such as polyvinylchloride to prevent the plastic from sticking to the hot surfaces in the machinery, which saves energy and enhances the material properties of products such as PVC pipes and profiles.
Oxidized PE Wax not only has excellent external lubricity, but also has a strong internal lubricating effect, and also has a coupling effect, which can improve the production efficiency of plastic processing and reduce production costs.


Using Oxidized PE Wax as plastic products processing lubricant can effectively improve demoulding, significantly reduce times of mould cleaning.
Oxidized PE Wax is mainly used for WPC & foaming material product, such as: PVC WPC foaming profile,plate,WPC building template,foaming profile,foaming board etc rigid product.


Oxidized PE Wax is widely used because of its excellent cold resistance, heat resistance, chemical resistance and wear resistance.
In normal production, Oxidized PE Wax can be added directly to polyolefin processing as an additive, which increases gloss and processing properties of the product.


As a lubricant, Oxidized PE Wax has stable chemical properties and good electrical properties.
Polyethylene wax is soluble in polyethylene, polypropylene, polyvinyl acetate, ethylene-propylene rubber and butyl rubber.
Oxidized PE Wax can improve the fluidity of polyethylene, polypropylene, ABS and the demoulding of polymethyl methacrylate and polycarbonate.


Oxidized PE Wax is used PVC heat stabilizer and profile, pipe, plate, etc.
After emulsification, Oxidized PE Wax is used for the paper industry, printing and dyeing, and garment industry,water-based ink, and water-based shoe polish.


Oxidized PE Wax is used in masterbatch, filler masterbatch, modified masterbatch, and functional masterbatch.
Oxidized PE Wax is used PVC heat stabilizer and profile, pipe, plate, etc.
After emulsification, Oxidized PE Wax is used for the paper industry, printing and dyeing and garment industry,water-based ink,water-based shoe polish;


Oxidized PE Wax is used Masterbatch, filler masterbatch, modified masterbatch,functional masterbatch;
Oxidized PE Wax is used Hot melt adhesive, adhesives.
Oxidized PE Wax is used Paint, coating, road marking paint.


Oxidized PE Wax can also be emulsified in water.
Wax emulsions are applied as finishes to textiles in order to obtain a smoother surface in order to make them easier to sew and to make them more resistant to linting and pilling.


Polyethylene waxes are used in polishes applied to shoes, furniture, floors and car bodywork and wax emulsions to protect the surface, to provide gloss or to enhance safety by increasing the slip resistance.
Addition of wax emulsions to the coating of glossy magazines protects the surface against ink rub-off.


A thin layer of Oxidized PE Wax can also be applied to the skin of citrus fruit to prevent it from drying out and becoming bruised.
Oxidized PE Wax as PVC profiles, pipes, plates, color masterbatch, processing aid, the dosage of 0.3 ~ 0.5% can improve the surface finish of processed products.


Oxidized PE Wax is used as hot melt adhesive and adhesives.
Oxidized PE Wax is used in paint, coating, and road marking paint.


-In the plastics processing industry, the internal and external lubrication effects of PVC are relatively balanced; adding Oxidized PE Wax to the hard, transparent and opaque PVC formulation has better lubricity than other lubricants.
Oxidized PE Wax is widely used in the production of PE, PVC cables, PVC profiles, pipes, and is an excellent new type of plastic processing lubricant.


-In rubber uses of Oxidized PE Wax:
Oxidized PE Wax has good compatibility with various rubbers.
Due to its high melting point and low viscosity, Oxidized PE Wax promotes good resin fluidity, relatively reduces the power consumption of resin mixing, and reduces the adhesion between resin and mold.
Oxidized PE Wax is easy to remove the film, plays a role of internal and external lubrication, and has good anti-static properties.


-Good emulsifying property, because a large amount of oxygen-containing groups are introduced during oxidation of Oxidized PE Wax, the interfacial tension during emulsification is lowered, so that a stable Oxidized PE Wax emulsion can be obtained, and reduced the amount of the emulsification agent, which is very important for the polish.


-Oxidized PE Wax has good compatibility with rubber, plastic, paraffin and other materials.
The internal and external lubrication of PVC is relatively balanced, the addition of Oxidized PE Wax to the rigid transparent PVC formulation is superior to other lubricants.


-Oxidized PE Wax is used in plastics:
Oxidized PE Wax can improve the production efficiency of the main plastic processing and reduce the production cost.

Adding Oxidized PE Wax to the hard, transparent and opaque PVC formula has better lubricity than other lubricants.
Oxidized PE Wax is widely used in PE, PVC cable materials, PVC profiles, PVC pipes, as well as raw and auxiliary materials for textile softening, car wax, and leather softener.


-Oxidized PE Wax is used in PVC foam boards:
Oxidized PE Wax is widely used in foam board. PVC foam board is the most difficult to produce in pvc products.
Oxidized PE Wax is the most difficult to solve the most problems.
Add Oxidized PE Wax, the plasticization can be accelerated obviously.


-The molecular chain of Oxidized PE Wax has a certain amount of carbonyl and hydroxyl groups.
The Oxidized PE Wax is an excellent new polar wax, so the compatibility with fillers, pigments and polar resins is significantly improved, lubricity and dispersibility.
Oxidized PE Wax is superior to polyethylene wax and also has coupling property.


-Oxidized polyethylene wax for pvc products
*Oxidized PE Wax can be used as PVC and other plastic lubricant.
*Oxidized PE Wax is excellent internal and external lubrication.
*Oxidized PE Wax can improve the lubricity between polymer and metal.
*Oxidized PE Wax can improve the dispersion of colorants.
*Give products good transparency and luster.
*Better improve production efficiency


-Coatings and Inks uses of Oxidized PE Wax:
Oxidized PE Wax finds extensive use in the coatings and ink industry.

Due to its excellent dispersibility and compatibility with other materials, Oxidized PE Wax is commonly employed as a dispersing agent, matting agent, and surface modifier in coatings and ink formulations.
Oxidized PE Wax’s ability to improve scratch resistance, gloss, and anti-blocking properties makes it an essential ingredient in these applications.


-Oxidized PE Wax has good compatibility with polyolefin resin, etc.
Oxidized PE Wax has good moisture resistance at normal temperature, strong chemical resistance, excellent electrical properties, improved appearance of finished products, low viscosity and high softening point.

Good hardness and other special properties, non-toxic, good thermal stability, low volatility at high temperature, excellent dispersion of fillers and pigments, excellent external lubricity, strong internal lubrication, and even together, Oxidized PE Wax can improve the production efficiency of plastic processing and reduce production costs.


-Oxidized PE Wax is commonly used in the production of PVC rigid products due to its excellent compatibility with PVC and its ability to improve various properties of the final product.
Here are some ways in which Oxidized PE Wax can be used in PVC rigid product manufacturing:

*Lubrication:
Oxidized PE Wax acts as a lubricant, reducing friction and improving the flow of PVC during processing.
This facilitates the extrusion or injection molding of PVC rigid products, resulting in improved surface finish and dimensional stability.

*Processing Aid:
Oxidized PE Wax can act as a processing aid, enhancing the fusion of PVC resins and improving the melt strength of the material.
Oxidized PE Wax can lead to increased productivity and reduced scrap rates during production.

*Impact Modification:
Oxidized PE Wax can be used as an impact modifier in PVC rigid products, improving their toughness and resistance to impact.
Oxidized PE Wax is particularly useful in applications where the product may be subjected to mechanical stresses or impacts, such as pipes or fittings.

*Anti-Blocking Agent:
Oxidized PE Wax can be used as an anti-blocking agent in PVC films, preventing them from sticking together during storage or transportation.
This improves handling and usability for end-users.

*Matting Effect:
Oxidized PE Wax can be used to impart a matting effect to PVC coatings and paints, resulting in a matte or satin finish.
This is useful in applications where a glossy appearance is not desired.

*Thermal Stability:
Oxidized PE Wax exhibits good thermal stability, allowing it to withstand high temperatures without significant degradation.
This property makes Oxidized PE Wax suitable for use in PVC rigid products that may be exposed to elevated temperatures during processing or use.


-PVC Stabilization uses of Oxidized PE Wax:
In the manufacturing of polyvinyl chloride (PVC) products, Oxidized PE Wax plays a crucial role as an external lubricant and processing aid.
Oxidized PE Wax helps improve the flow properties of PVC compounds, reducing processing difficulties and enhancing the final product’s surface finish.
Additionally, Oxidized PE Wax acts as a heat stabilizer for PVC, improving the material’s resistance to thermal degradation during processing.


-Textile and Leather Processing uses of Oxidized PE Wax:
Oxidized PE Wax finds applications in the textile and leather industries as a softening agent and lubricant.
In textile processing, Oxidized PE Wax imparts a smooth, soft feel to fabrics and enhances their dye receptivity.
In leather processing, Oxidized PE Wax aids in achieving uniform colour distribution and improved water repellency in leather products.


-Adhesives and Sealants uses of Oxidized PE Wax:
The addition of Oxidized PE Wax to adhesives and sealants can improve their performance in various ways.
Oxidized PE Wax acts as a flow and rheology modifier, reducing viscosity and enhancing workability during application.
Additionally, Oxidized PE Wax helps enhance the adhesion and wetting properties of adhesives and sealants, resulting in stronger and more durable bonds.


-Masterbatches and Compounds uses of Oxidized PE Wax:
Oxidized PE Wax is often used as a processing aid in the production of masterbatches and compounds.
Oxidized PE Wax improves the dispersion of pigments, fillers, and additives in the polymer matrix, leading to more uniform and consistent final products.
Furthermore, Oxidized PE Wax’s lubricating properties facilitate better melt flow, reducing energy consumption during processing.


-Rubber and Tire Industry uses of Oxidized PE Wax:
In the rubber and tire industry, Oxidized PE Wax is employed as a lubricant and processing aid during the compounding and shaping processes.
Oxidized PE Wax helps prevent the sticking of rubber compounds to processing equipment, resulting in smoother and more efficient production.
Additionally, Oxidized PE Wax contributes to the enhancement of the finished rubber product’s surface properties.



FEATURES OF OXIDIZED PE WAX:
1. Oxidized PE Wax has obviously improved fabric, paper, leather products and coating film hand sensibility, smoothness, light resistance, smooth softness good function;
2. Oxidized PE Wax is used in the production of high performance coating anti-settling wax slurry, textiles slip agent (cowboy cloth material), printing paste, wax emulsion, floor polishes, fruit fresh paint, oil polish and so on;
3. Oxidized PE Wax is used for water paint, paper, leather industry, a new generation of high quality brightener;
4. Oxidized PE Wax thermal stability is good, not yellow. In the textile industry, mainly used for softening agent and sizing agent, finishing agent.
Make the finished fabric have a soft and smooth handle, at the same time improve the physical properties of the fabric.
5. In man-made board industry, instead of paraffin waterproofing agent can get obvious effect;
6. Polyurethane unemployment and other process good release agent;
7. Oxidized PE Wax acid and alkali resistance, good chemical stability.
8. Oxidized PE Wax non-toxic, no corrosion, non-inflammable non-dangerous goods, do not contain the free formaldehyde, APEO, phosphorus, etc. Is environmental protection product.



PROPERTIES OF OXIDIZED PE WAX:
Oxidized PE Wax contains some hydroxyls in its molecular chain, which greatly improves its compatibility with polar resins, superior to PE wax in this regard.

Oxidized PE Wax has good internal and external lubricity, thus it can achieve better lubricating properties than the other lubricants when used in the formula of rigid transparent or opaque PVC products.

Oxidized PE Wax also widely applies to PE or PVC cables, PVC profiles, and pipe as new-type plastic lubricants and can be used as raw or auxiliary material for textile softener, auto wax, and leather softener.
Oxidized PE Wax has good chemical durability, soluble in aromatic hydrocarbon.



ADVANTAGES OF OXIDIZED PE WAX:
1. Oxidized PE Wax can be used as PVC and other plastic lubricant.
2. Excellent internal and external lubrication.
3, Oxidized PE Wax can improve the lubricity between polymer and metal.
4, Oxidized PE Wax can improve the dispersion of colorants.
5, Give products good transparency and luster.
6. Better improve production efficiency



CHEMICAL COMPOSITION OF OXIDIZED PE WAX:
the molecular chain of Oxidized PE Wax has certain functional groups, so the solubility of it and polar resin can be improved significantly, which is better than that of polyethylene wax.



ADVANTAGES OF OXIDIZED PE WAX:
Oxidized PE Wax is made from polyethylene wax by special oxidation process.
Oxidized PE Wax has low viscosity, high softening point, good hardness and other special properties.
In PVC system, low density Oxidized PE Wax can be plasticized ahead of time, and the later torque is reduced.
Oxidized PE Wax has excellent internal and external lubrication.



WHAT IS THE DIFFERENCE BETWEEN OXIDIZED PE WAX AND POLYETHYLENE WAX?
Oxidized PE Wax is a bright plastic auxiliaries for internal and external lubrication.
Oxidized PE Wax is mainly produced by using polyethylene paraffin stearate stearic acid sulphate heated in a reaction vessel to a temperature of 380 °C for 6 to 8 hours.

The difference between Oxidized PE Wax and polyethylene wax is that the Oxidized PE Wax contains a modified wax product of a polar gene, so that the properties of Oxidized PE Wax such as durability and polishing are much better than polyethylene wax.

The chemical properties of Oxidized PE Wax are more stable than polyethylene wax, non-toxic and non-corrosive, and make Oxidized PE Wax more widely used.
Oxidized PE Wax is a versatile and highly beneficial material that offers numerous advantages in various industries.

One key advantage of Oxidized PE Wax lies in its excellent lubricating properties.
Due to its low coefficient of friction, Oxidized PE Wax can effectively reduce friction between surfaces, resulting in reduced wear and tear on equipment and machinery.

This characteristic makes Oxidized PE Wax an ideal additive for industrial applications such as plastic processing, rubber compounding, and coatings formulation.

Additionally, Oxidized PE Wax exhibits outstanding dispersibility, meaning it can be easily incorporated into different mediums without clumping or settling.
This feature of Oxidized PE Wax allows for even distribution throughout the desired materials, enhancing their overall performance and stability.



ADVANTAGES OF OXIDIZED PE WAX:
Oxidized PE Wax is a versatile and highly advantageous material that offers numerous benefits across various industries.
One key advantage of Oxidized PE Wax lies in its exceptional lubricating properties.
Due to its low coefficient of friction, Oxidized PE Wax reduces the friction between surfaces, facilitating smooth movement and reducing wear and tear.

Moreover, Oxidized PE Wax exhibits excellent heat stability, making it an ideal choice for applications involving high temperatures.
Oxidized PE Wax's resistance to chemicals further enhances its utility in industries where exposure to corrosive substances is common.

Another significant advantage is Oxidized PE Wax's ability to improve the flow characteristics of materials during processing or manufacturing processes like extrusion or injection molding.

This property not only aids in achieving more precise end products but also increases production efficiency by minimizing downtime caused by equipment clogging or jamming issues.

Additionally, Oxidized PE Wax acts as an effective dispersant, allowing for better distribution of pigments and fillers within formulations such as paints or coatings, resulting in improved coloration and overall quality of the final product.



CHARACTERISTICS OF OXIDIZED PE WAX:
Oxidized PE Wax has good compatibility with PVC and other PVC additives.
Oxidized PE Wax is suitable for many kinds of processing conditions, it can improve fusion, melt, impact strength and surface gloss.
Oxidized PE Wax can be widely used in transparent sheets, granules, window profiles, board, and pipes.



MARKET OVERVIEW AND REPORT COVERAGE OF OXIDIZED PE WAX:
Oxidized PE Wax is a type of polyethylene wax that is produced by oxidation of low molecular weight polyethylene.
Oxidized PE Wax is commonly used as a lubricant, dispersant, and processing aid in various industries, including plastics, coatings, adhesives, and rubber.

The future outlook of the Oxidized PE Waxmarket is positive and promising.
The market of Oxidized PE Wax is expected to witness steady growth during the forecast period.
Technological advancements and innovations in the production of Oxidized PE Wax is likely to drive market growth.

The increasing demand for Oxidized PE Wax from end-use industries, such as packaging, textiles, and paints, is another major factor contributing to the growth of the market.
The current outlook of the Oxidized PE Wax market is also favorable.

The market is experiencing steady growth due to the wide range of applications of Oxidized PE Wax in different industries.
The demand for Oxidized PE Wax is particularly high in the plastics industry, where it is used as a lubricant and release agent.

The rising demand for plastic products from various sectors, including automotive, construction, and packaging, is driving the growth of the Oxidized PE Wax market.
Moreover, the growing awareness about the benefits of Oxidized PE Wax, such as its low melting point, excellent dispersion, and improved processing characteristics, is further fueling market growth.

Additionally, the market of Oxidized PE Wax is witnessing the emergence of new players and the expansion of existing manufacturers, leading to increased competition and product innovation.
However, challenges such as fluctuating raw material prices and environmental concerns regarding the disposal of Oxidized PE Wax may impede market growth to some extent.

Nevertheless, the overall outlook for the Oxidized PE Wax market remains positive, with a projected compound annual growth rate (CAGR) of % during the forecast period mentioned.



CHARACTERISTICS AND PURPOSES OF OXIDIZED PE WAX:
1. Oxidized PE Wax is a synthetic wax.
Oxidized PE Wax has different melting point, hardness, and density, polyethylene wax is a very good choice under the high temperature condition.

Oxidized PE Wax emulsion refers to the water-based system with the particle size distribution below 1 μ m, distinguished by the emulsion iconicity, it can be non-ionic, anionic, and cationic.
Oxidized PE Wax emulsion is different from wax dispersion, it has no matting effect, and be used for coating and inks which has high requirement on gloss.


2. Oxidized PE Wax with high gloss and high transparency, can improve hand-feeling, abrasion&scratch resistance, especially suitable for coatings that need high gloss and transparency.


3. Oxidized PE Wax is used for fabric finish, coating, ink, paper, leather, B-26 provides abrasion&scratch resistance, high gloss and soft hand-feeling.


4. Oxidized PE Wax can be used for water-based coatings, and polish fields like floor, leather, furniture, automotive, paper and others, as well as the production of liquid shoe polish, metal mold release agents, and other industries.


5. When added into the leather finishing agents, Oxidized PE Wax can increase the leather feeling and abrasion resistance; when added into color paste, it can provide flatting effectand can prevent the coating from stickiness when meet heat.



PROPERTIES OF OXIDIZED PE WAX:
Oxidized PE Wax contains functional groups (acid and Ester groups) causing improved compatibility with the PVC melt.
In the extrusion process Oxidized PE Wax provides efficient external lubrication that helps to maintain premium physical and aesthetic properties under high shear operating conditions.
Thanks to their polar group Oxidized PE Wax has an affinity to metal surfaces providing external release.



HOW IS OXIDIZED PE WAX MADE:
Oxidized PE Wax is a polar reaction product resin produced by mild air oxidation of polyethylene so that it produces a minimum average molecular weight of 1,200 as determined by high temperature vapor pressure.



CHEMICAL CHARACTERISTIC OF OXIDIZED PE WAX:
Oxidized PE Wax has low adhesive, high softening point, and good hardness with stable chemical characteristics of good heat stability, good dispersion performance, no poison, no frost, and mucous membrane; as an ideal interior & exterior lubricant.



ADVANTAGES OF OXIDIZED PE WAX:
1, Oxidized PE Wax can be used as PVC and other plastic lubricant.
2. Excellent internal and external lubrication.
3, Oxidized PE Wax can improve the lubricity between polymer and metal.
4, Oxidized PE Wax can improve the dispersion of colorants.
5, Give products good transparency and luster.
6. Better improve production efficiency



CHEMICAL CHARACTERISTIC OF OXIDIZED PE WAX:
Low adhesive, high softening point and good hardness with stable chemical characteristics of good heat stability, good dispersion performance, no poison, no frost and mucous membrane; as an ideal interior & exterior lubricant, Oxidized PE Wax can be used as a substitute for liquid paraffin, natural paraffin etc



PROPERTIES OF OXIDIZED PE WAX:
Oxidized PE Wax is a white particle,flake or powder, with good lubricant effect, chemical durability and good electrical performance, soluble in aromatic hydrocarbon.



FEATURES OF OXIDIZED PE WAX:
1. Improved Compatibility:
Oxidized PE Wax exhibits enhanced compatibility with polar materials, such as polyvinyl chloride (PVC), polypropylene (PP), and various coatings.
This compatibility facilitates better dispersion and adhesion of Oxidized PE Wax in these materials, leading to improved performance and stability.

2. Lubrication and Slip Resistance:
Oxidized PE Wax offers excellent lubricating properties, reducing friction and improving the slip resistance of various products.
Oxidized PE Wax can be used as an additive in coatings, inks, and plastics to enhance surface properties and facilitate processing.

3. Matting Effect:
When used in coatings and paints, Oxidized PE Wax can impart a matting effect, resulting in a matte or satin finish.
This is particularly useful in applications where a glossy appearance is not desired.

4. Improved Rheological Properties:
Oxidized PE Wax can modify the rheological properties of formulations, such as viscosity and flow behavior.
Oxidized PE Wax can act as a rheology modifier, improving the processability and application characteristics of various systems.

5. Thermal Stability:
Oxidized PE Wax exhibits good thermal stability, allowing it to withstand high temperatures without significant degradation.
This property makes Oxidized PE Wax suitable for applications requiring heat resistance, such as hot-melt adhesives and coatings.

6. Anti-blocking Properties:
Oxidized PE Wax can be used as an anti-blocking agent in films, preventing them from sticking together during storage or transportation.
This improves handling and usability for end-users.



OXIDIZED PE WAX OFFERS SEVERAL ADVANTAGES, INCLUDING:
1. Improved Surface Properties:
Oxidized PE Wax is known to improve the surface properties of materials, such as scratch resistance and slip resistance.
Oxidized PE Wax can provide a smooth and glossy finish to products and enhance their durability.

2. Enhanced Processibility:
Oxidized PE Wax can improve the processing characteristics of materials, making them easier to handle and process.
Oxidized PE Wax can reduce the friction between surfaces during processing, leading to improved flow and reduced processing time.

3. High Thermal Stability:
Oxidized PE Wax has high thermal stability and can withstand temperatures up to 150°C without degradation.
This makes Oxidized PE Wax suitable for use in high-temperature applications such as hot-melt adhesives and coatings.

4. Low Volatility:
Oxidized PE Wax has low volatility, meaning it doesn't easily evaporate into the air.
This makes Oxidized PE Wax suitable for use in products where low odor and emissions are important, such as food packaging materials.

5. Compatibility:
Oxidized PE Wax is compatible with a wide range of polymers, including polyethylene, polypropylene, polystyrene, and PVC.
This makes Oxidized PE Wax a versatile additive that can be used in various applications.



WHAT IS THE DIFFERENCE BETWEEN OXIDIZED PE WAX AND POLYETHYLENE WAX?
PE wax is non-oxidized wax, Oxidized PE Wax is oxidized wax, with a certain acid value, oxidized wax molecular chain with a certain amount of carbonyl and hydroxyl, oxidized polyethylene wax is excellent new polar wax, so the compatibility with fillers, pigments, polar resins is significantly improved, lubricity, dispersion is better than polyethylene wax, but also both coupling properties.

Polyethylene wax has good compatibility with polyethylene, polypropylene, polyvinyl chloride, ethylene propylene rubber and butyl rubber.
It can improve the fluidity of polyethylene, polypropylene, ABS and the demoulding of polymethyl methacrylate and polycarbonate.
For PVC and other external lubricants, polyethylene wax has stronger internal lubricating effect compared with other external lubricants.



PHYSICAL and CHEMICAL PROPERTIES of OXIDIZED PE WAX:
Softening point (°C): 90-110
Density (g/cm3): 0.94-0.96
Acid index (mg KOH/g): 12-15
Acid value: 10 - 13 KOH mg/g 13 - 16
KOH mg/g 4 - 10 KOH mg/g
Softening Point℃: 100-105
ViscosityCPS@140℃: 200-300
Acid Value Mg KOH/g: 15-20
Appearance: White bead
Appearance: white powder with light yellow
Molecular weight: 3,000-4,000



FIRST AID MEASURES of OXIDIZED PE WAX:
-Description of first-aid measures:
*If inhaled:
If breathed in, move person into fresh air.
*In case of skin contact:
Wash off with soap and plenty of water.
*In case of eye contact:
Flush eyes with water as a precaution.
*If swallowed:
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of OXIDIZED PE WAX:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Keep in suitable, closed containers for disposal.



FIRE FIGHTING MEASURES of OXIDIZED PE WAX:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available



EXPOSURE CONTROLS/PERSONAL PROTECTION of OXIDIZED PE WAX:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
*Body Protection:
Impervious clothing
*Respiratory protection:
Respiratory protection not required.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of OXIDIZED PE WAX:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.



STABILITY and REACTIVITY of OXIDIZED PE WAX:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available

OXODECANEDIOIC ACID
Oxodecanedioic acid is an organic dicarboxylic acid.
Oxodecanedioic acid is a naturally occurring dicarboxylic acid with the chemical formula (CH2)8(CO2H)2.
Oxodecanedioic acid is a white flake or powdered solid.

CAS Number: 111-20-6
EC Number: 203-845-5
Chemical Formula: HOOC(CH₂)₈COOH
Molar Mass: 202.25 g/mol

Oxodecanedioic acid is a naturally occurring dicarboxylic acid with the chemical formula HO2C(CH2)8CO2H.
Oxodecanedioic acid is a white flake or powdered solid.

Sebaceus is Latin for tallow candle, sebum is Latin for tallow, and refers to its use in the manufacture of candles.
Oxodecanedioic acid is a derivative of castor oil.

In the industrial setting, Oxodecanedioic acid and its homologues such as azelaic acid can be used as a monomer for nylon 610, plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.
Oxodecanedioic acid can be used as a surfactant in the lubricating oil industry to increase the antirust properties of lubricating oils on metals.

Oxodecanedioic acid is a white granular powder.
Oxodecanedioic acid has Melting point of 153 °F.
Oxodecanedioic acid is Slightly soluble in water.

Oxodecanedioic acid is a white granular powder.
Melting point of Oxodecanedioic acid is 153 °F.

Oxodecanedioic acid is slightly soluble in water.
Sebaceus is Latin for tallow candle, sebum is Latin for tallow, and refers to Oxodecanedioic acid is use in the manufacture of candles.

Oxodecanedioic acid is an alpha,omega-dicarboxylic acid that is the 1,8-dicarboxy derivative of octane.
Oxodecanedioic acid has a role as a human metabolite and a plant metabolite.

Oxodecanedioic acid was named from the Latin sebaceus (tallow candle) or sebum (tallow) in reference to Oxodecanedioic acid is use in the manufacture of candles.
Oxodecanedioic acid sublimes slowly at 750 mmHg when heated to melting point.

Oxodecanedioic acid is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 tonnes per annum.
Oxodecanedioic acid is a urinary metabolite that has been identified as an anti-fatigue biomarker.

In Oxodecanedioic acid's purest form, Oxodecanedioic acid is a powdered crystal or white flaky substance.
In Oxodecanedioic acid's pure state Oxodecanedioic acid is a white flake or powdered crystal.
Oxodecanedioic acid is described as non-hazardous, though in its powdered form Oxodecanedioic acid can be prone to flash ignition (a typical risk in handling fine organic powders).

Sebaceus is Latin for tallow candle, sebum (tallow) is Latin for tallow, and refers to its use in the manufacture of candles.
Oxodecanedioic acid is white flaky crystals.
Oxodecanedioic acid is slightly soluble in water, soluble in alcohol and ether.

Oxodecanedioic acid is also the raw material for the production of alkyd resins (used as surface coatings, plasticized nitrocellulose coatings, and urea resin varnishes) and polyurethane rubber, cellulose resins, vinyl resins, and synthetic rubber plasticizers, softeners, and solvents.
Oxodecanedioic acid’s a naturally occurring dicarboxylic acid that is non-hazardous, though Oxodecanedioic acid can be vulnerable to flash ignition in its powder form.

One of the most common uses for Oxodecanedioic acid is in the manufacturing of candles.
Oxodecanedioic acid sublimes slowly at 750 mm Hg when heated to melting point.;DryPowder; DryPowder, PelletsLargeCrystals; OtherSolid; PelletsLargeCrystals;Solid;WHITE POWDER WITH CHARACTERISTIC ODOUR.

Oxodecanedioic acid also shows up in the industrial industry, being used as a monomer and intermediate for various products and materials.
Oxodecanedioic acid is white flaky crystal.
Oxodecanedioic acid is slightly soluble in water, soluble in alcohol and ether.

Oxodecanedioic acid is a derivative of castor oil, with the vast majority of world production occurring in China which annually exports over 20,000 metric tonnes, representing over 90 % of global trade of the product.
Oxodecanedioic acid is produced from castor oil.

Oxodecanedioic acid is an alpha,omega-dicarboxylic acid and a dicarboxylic fatty acid.
Oxodecanedioic acid is a conjugate acid of a sebacate(2-) and a sebacate.

Oxodecanedioic acid is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 tonnes per annum.
Oxodecanedioic acid’s mostly colorless but can be a light shade of yellow.

Oxodecanedioic acid is a saturated, straight-chain naturally occurring dicarboxylic acid with 10 carbon atoms.
Oxodecanedioic acid is a normal urinary acid.

Oxodecanedioic acid is a saturated, straight-chain naturally occurring dicarboxylic acid with 10 carbon atoms.
Oxodecanedioic acid is a normal urinary acid.

Oxodecanedioic acid is an acid derived from castor oil.
Oxodecanedioic acid is sold in the form of a white, granular powder and sometimes referred to by either of Oxodecanedioic acid is chemical names: 1,8-octanedicarboxylic acid.

Oxodecanedioic acid is a white flake or powdered crystal slightly soluble in water that has been proposed as an alternative energy substrate in total parenteral nutrition.
Oxodecanedioic acid also has a mild odor to it, though nothing that stands out.

There are two ways that Oxodecanedioic acid can be produced: castor oil and adipic acid.
Oxodecanedioic acid is a white flake or powdered crystal slightly soluble in water that has been proposed as an alternative energy substrate in total parenteral nutrition.
Oxodecanedioic acid’s far more common for Oxodecanedioic acid to be derived from castor oil, as the process is green and cost effective.

To make the Oxodecanedioic acid, the castor oil is heated to high temperatures with alkali.
Oxodecanedioic acid was named from the Latin sebaceus (tallow candle) or sebum (tallow) in reference to its use in the manufacture of candles.
Oxodecanedioic acid is a white granular powder.

The purity of Oxodecanedioic acid is based on the type of reaction it has.
Generally, modern conversion technology leads to a purer product.
Oxodecanedioic acid's Melting point is 153°F.

Oxodecanedioic acid is slightly soluble in water.
Oxodecanedioic acid is a saturated, straight-chain naturally occurring dicarboxylic acid with 10 carbon atoms.

Oxodecanedioic acid belongs to the class of organic compounds known as medium-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.

Oxodecanedioic acid is made from castor oil and belongs to the homologous series of dicarboxylic acids.
The best known application of Oxodecanedioic acid is the production of polyamides.

Oxodecanedioic acid, a dicarboxylic acid with structure (HOOC) (CH2)8(COOH), is a naturally occurring chemical derivative of castor oil which has been proven safe in vivo.
Oxodecanedioic acid is a normal urinary acid.

Oxodecanedioic acid is a natural product found in Isatis tinctoria, Euglena gracilis, and other organisms with data available.
Oxodecanedioic acid is a natural C10 liquid fatty acid, directly produced from castor oil.

Oxodecanedioic acid is found to be associated with carnitine-acylcarnitine translocase deficiency and medium chain acyl-CoA dehydrogenase deficiency, which are inborn errors of metabolism.
Oxodecanedioic acid is a saturated, straight-chain naturally occurring dicarboxylic acid with 10 carbon atoms.

Oxodecanedioic acid is a normal urinary acid.
Oxodecanedioic acid is a white flake or powdered crystal slightly soluble in water that has been proposed as an alternative energy substrate in total parenteral nutrition.

Oxodecanedioic acid was named from the Latin sebaceus (tallow candle) or sebum (tallow) in reference to its use in the manufacture of candles.
Oxodecanedioic acid and its derivatives such as azelaic acid have a variety of industrial uses as plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.

Oxodecanedioic acid has a role as a human metabolite and a plant metabolite.
Oxodecanedioic acid is an alpha,omega-dicarboxylic acid and a dicarboxylic fatty acid.

Oxodecanedioic acid is a conjugate acid of a sebacate(2-) and a sebacate.
Oxodecanedioic acid derives from a hydride of a decane.

Oxodecanedioic acid acts as a plasticizer, solvent and softener.
Oxodecanedioic acid is a white flake or powdered solid.

Sebaceus is Latin for tallow candle, sebum is Latin for tallow, and refers to its use in the manufacture of candles.
Oxodecanedioic acid is manufactured by splitting of castor oil followed by fusion with caustic.

Oxodecanedioic acid sublimes slowly at 750 mmHg when heated to melting point.
Oxodecanedioic acid is an alpha,omega-dicarboxylic acid that is the 1,8-dicarboxy derivative of octane.

Oxodecanedioic acid is white crystalline powder or granular form slightly dissolves in water, completely dissolves in ethanol or ether but not in benzene.
Oxodecanedioic acid is high end derivative of castor oil and Oxodecanedioic acid is also called "Sebacic Acid".

Oxodecanedioic acid's Melting point is 153 °F.
Oxodecanedioic acid is slightly soluble in water.

Oxodecanedioic acid is a derivative of castor oil.
Oxodecanedioic acid is a white granular powder.

Oxodecanedioic acid is a natural liquid fatty acid, directly produced from castor oil.
Oxodecanedioic acid is a derivative of castor oil.

Oxodecanedioic acid is an organic dicarboxylic acid.
Oxodecanedioic acid is a naturally occurring dicarboxylic acid with the chemical formula (CH2)8(CO2H)2.

Oxodecanedioic acid is an alpha,omega-dicarboxylic acid that is the 1,8-dicarboxy derivative of octane.
Oxodecanedioic acid has a role as a human metabolite and a plant metabolite.

Oxodecanedioic acid is an alpha,omega-dicarboxylic acid and a dicarboxylic fatty acid.
Oxodecanedioic acid is a conjugate acid of a sebacate(2-) and a sebacate.

Oxodecanedioic acid derives from a hydride of a decane.
Oxodecanedioic acid is a natural product found in Isatis tinctoria, Euglena gracilis, and other organisms with data available.

Oxodecanedioic acid is a saturated, straight-chain naturally occurring dicarboxylic acid with 10 carbon atoms.
Oxodecanedioic acid is a normal urinary acid.

In patients with multiple acyl-CoA-dehydrogenase deficiency (MADD) or glutaric aciduria type II (GAII) are a group of metabolic disorders due to deficiency of either electron transfer flavoprotein or electron transfer flavoprotein ubiquinone oxidoreductase, biochemical data shows an increase in urine Oxodecanedioic acid excretion.
Oxodecanedioic acid is a white flake or powdered crystal slightly soluble in water that has been proposed as an alternative energy substrate in total parenteral nutrition.

Oxodecanedioic acid was named from the Latin sebaceus (tallow candle) or sebum (tallow) in reference to its use in the manufacture of candles.
Oxodecanedioic acid is a dicarboxylic acid obtained from the dry distillation of castor oil.

Oxodecanedioic acid is derived from castor oil.
Two molecules are needed to obtain a castor Oxodecanedioic acid.
Castor oil is obtained from the fruit seed of castor (Ricinus communis L.) a large shrub that grows mainly in India, Brazil and China.

The seed has an oil content of 40-50%.
Oxodecanedioic acid is solid at room temperature and melts above 130°C.

Oxodecanedioic acid is in the form of white crystalline solid (powder or granules depending of the manufacturer).
Stabilizer in alkyd resins, maleic and other polyesters, polyurethanes, fibers, paints, candles and perfumes, low temperature lubricants and hydraulic fluids.

Oxodecanedioic acid derives from a hydride of a decane.
Oxodecanedioic acid is a naturally occurring dicarboxylic acid which is a derivative of castor oil.

Oxodecanedioic acid is a white flake or powdered crystal slightly soluble in water that has been proposed as an alternative energy substrate in total parenteral nutrition.
Oxodecanedioic acid is a dicarboxylic acid with structure (HOOC)(CH2)8(COOH), and is naturally occurring.

Uses of Oxodecanedioic acid:
Oxodecanedioic acid is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Oxodecanedioic acid is used in the synthesis of polyamide and alkyd resins.

Oxodecanedioic acid is also used as an intermediate for aromatics, antiseptics and painting materials.
In the industrial setting, Oxodecanedioic acid and its homologues such as azelaic acid can be used in plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.

Oxodecanedioic acid is also used as an intermediate for aromatics, antiseptics, and painting materials.
Oxodecanedioic acid is used in the following products: washing & cleaning products, adhesives and sealants, fuels, lubricants and greases, coating products and fertilisers.

Release to the environment of Oxodecanedioic acid can occur from industrial use: of substances in closed systems with minimal release.
Release to the environment of Oxodecanedioic acid can occur from industrial use: of substances in closed systems with minimal release.

Oxodecanedioic acid also works as a buffering & neutralizing agent.
Other release to the environment of Oxodecanedioic acid is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).

Oxodecanedioic acid is used in skin care, hair care and sun care formulations.
Oxodecanedioic acid is used as a topical emollient.

Oxodecanedioic acid and its derivatives such as azelaic acid have a variety of industrial uses as plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.
Oxodecanedioic acid is used in the synthesis of polyamide and alkyd resins.

Oxodecanedioic acid can be used as a corrosion inhibitor in metalworking fluids and as a complexing agent in greases.

Release to the environment of Oxodecanedioic acid can occur from industrial use: formulation of mixtures and in the production of articles.
Other release to the environment of Oxodecanedioic acid is likely to occur from: indoor use and outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives).
Oxodecanedioic acid can be found in products with material based on: plastic (e.g. food packaging and storage, toys, mobile phones) and leather (e.g. gloves, shoes, purses, furniture).

Oxodecanedioic acid is used in the following products: biocides (e.g. disinfectants, pest control products), pH regulators and water treatment products, laboratory chemicals, plant protection products, water softeners and water treatment chemicals.
Oxodecanedioic acid is used in the following areas: formulation of mixtures and/or re-packaging and agriculture, forestry and fishing.

Oxodecanedioic acid is used for the manufacture of: chemicals.
Other release to the environment of Oxodecanedioic acid is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.

Oxodecanedioic acid is used in the following products: adhesives and sealants, polymers, coating products, lubricants and greases and cosmetics and personal care products.
In the industrial setting, Oxodecanedioic acid and its homologues such as azelaic acid can be used as a monomer for nylon 610, plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.

Oxodecanedioic acid is a urinary metabolite that has been identified as an anti-fatigue biomarker.
Oxodecanedioic acid and its derivatives such as azelaic acid have a variety of industrial uses as plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.
Oxodecanedioic acid is used in the synthesis of polyamide and alkyd resins.

Release to the environment of Oxodecanedioic acid can occur from industrial use: formulation of mixtures, in processing aids at industrial sites, as processing aid, as an intermediate step in further manufacturing of another substance (use of intermediates), for thermoplastic manufacture, manufacturing of the substance and formulation in materials.

Oxodecanedioic acid can be used as plasticizers for plastics and cold-resistant rubber, as well as for polyamide, polyurethane, alkyd resin, synthetic lubricating oil, lubricating oil additives, spices, coatings, cosmetics, etc.
Oxodecanedioic acid is used in the following products: laboratory chemicals, water treatment chemicals, pH regulators and water treatment products, water softeners and polymers.

Oxodecanedioic acid is widely used in the preparation of Oxodecanedioic acid esters, such as dibutyl sebacate, dioctyl sebacate, diisooctyl sebacate.
Oxodecanedioic acid is used in the following areas: formulation of mixtures and/or re-packaging.

Oxodecanedioic acid and its derivatives such as azelaic acid have a variety of industrial uses as plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.
Oxodecanedioic acid is also used as an intermediate for aromatics, antiseptics and painting materials.

Oxodecanedioic acid is used as source material for various products.
In addition, Oxodecanedioic acid is used as a crosslinker in the adhesives industry, as a plasticizer in the plastics industry, as a component of lubricants and as an extender in packaging films.

Oxodecanedioic acid is used for the manufacture of: chemicals, plastic products and rubber products.
Oxodecanedioic acid can be used as a synthesis intermediate for sebacates esters which can be used as emollients, masking agent, film forming agent, hair or skin conditioning agent, SPF Booster, etc.

Release to the environment of Oxodecanedioic acid can occur from industrial use: in processing aids at industrial sites, in the production of articles, formulation of mixtures, as an intermediate step in further manufacturing of another substance (use of intermediates), as processing aid and for thermoplastic manufacture.
Oxodecanedioic acid can also be used as raw material for producing nylon 1010, nylon 910, nylon 810, nylon 610, nylon 9 and high temperature resistant lubricating oil diethylhexyl ester.

Oxodecanedioic acid is also used as an intermediate for aromatics, antiseptics and painting materials.
Release to the environment of Oxodecanedioic acid can occur from industrial use: manufacturing of the substance.
In the industrial setting, Oxodecanedioic acid and its homologues such as azelaic acid can be used as a monomer for nylon 610, plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.

Oxodecanedioic acid can be used as a surfactant in the lubricating oil industry to increase the antirust properties of lubricating oils on metals.
Oxodecanedioic acid is used in the following products: washing & cleaning products, adhesives and sealants, fuels, lubricants and greases, coating products and fertilisers.

Oxodecanedioic acid and its derivatives such as azelaic acid have a variety of industrial uses as plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.
Oxodecanedioic acid is used in the synthesis of polyamide and alkyd resins.

Oxodecanedioic acid is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Oxodecanedioic acid is also used as an intermediate for aromatics, antiseptics and painting materials.

Sebaceus is Latin for tallow candle, and sebum is Latin for tallow. These terms refer to the use of Oxodecanedioic acid in the manufacturing of candles.
In particular, Oxodecanedioic acid is used as a thickener in lithium complex grease.

In addition, Oxodecanedioic acid can be used as an intermediate in the production of aromatics, antiseptics and painting materials as well as in the synthesis of polyamide and alkyd resins.
Oxodecanedioic acid is also used in the synthesis of polyamide, as nylon, and of alkyd resins.

But as stated above, Oxodecanedioic acid has a lot of uses for the industrial setting.
Oxodecanedioic acid's anti-corrosive properties make Oxodecanedioic acid a useful addition to metalworking fluids and antifreeze.

Oxodecanedioic acid is also an additive and thickener for grease and lubricants, as well as an intermediate in paints and other coatings.
When used in a mixture with other dibasic acids Oxodecanedioic acid is especially effective as a ferrous corrosion inhibitor for metalworking fluids, engine coolants, metal cleaners, aqueous hydraulic fluids.

Oxodecanedioic acid can also be used as a complexing agent for lithium complex grease which will increase dropping point and improve mechanical stability.
Other release to the environment of this substance is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).

Oxodecanedioic acid is used as a raw material for alkyd and polyester resins, plasticizers, polyester rubbers, and polyamide synthetic fibers.
Oxodecanedioic acid can be used as a monomer for nylon, lubricants, hydraulic fluids, cosmetics, plasticizers and more.

Oxodecanedioic acid can also be used as an intermediate for antiseptics, aromatics and painting products.
Oxodecanedioic acid is used in the synthesis of polyamide and alkyd resins.

Oxodecanedioic acid is also used as an intermediate for aromatics, antiseptics and painting materials.
Oxodecanedioic acid is used as a stabilizer in alkyd resins, maleic and other polyesters, polyurethanes, and fibers.

Oxodecanedioic acid is also used in paint products, candles, perfumes, low temperature lubricants, and hydraulic fluids, and to make nylon.
Oxodecanedioic acid is largely used in the manufacturing process of Nylon 6-10.

An isomer, isoOxodecanedioic acid, has several applications in the manufacture of vinyl resin plasticizers, extrusion plastics, adhesives, ester lubricants, polyesters, polyurethane resins and synthetic rubber.
Oxodecanedioic acid can also be found in plasticizers, lubricants, hydraulic fluids, cosmetics, and candle manufacturing.

In cosmetics, Oxodecanedioic acid can be used as a buffering ingredient for pH adjustment or a chemical intermediate in the synthesis of various esters.
DoOxodecanedioic acid is mainly used in top-grade powder coatings and paint, adhesives, pulp & paper, chemical and industrial facilities, surfactants, antiseptics.

In combination with Amine, Oxodecanedioic acid is used to produce engineering plastics polyamide resins wich is a high performance nylon 6-12, adhesives, diester synthetic lubricants, fibers, curatives, plasticizers, polyester coatings, epoxy resins.
Due to Oxodecanedioic acid's smoothing and conditioning properties, Jamaican black castor oil is ideal for use in products like cleansers, moisturizers, and ethnic hair care products.

Oxodecanedioic acid was historically used in candle-making and today has many functions in manufacturing and industrial processing.
Some of the principal uses of Oxodecanedioic acid include acting as an intermediate in nylon, synthetic resins and other plastics.
Oxodecanedioic acid and its derivatives, as azelaic acid, have a variety of industrial uses as plasticizers, lubricants, diffusion pump oils, cosmetics, candles, etc.

Lubricants, Plastics and Greases use:
The fatty acids in castor oil give Oxodecanedioic acid excellent lubricating properties.
You can choose either traditional castor oil or Jamaican black castor oil as a lubricant in metal drawing and other industrial processes.

Such as:
Plasticizers
Lubricants
Hydraulic Fluids
Cosmetics
Candles
Buffering
pH Regulating Agent
pH Adjuster
Adhesives & Sealants
Paints & Coatings
Personal Care Products

Metalworking Fluids uses:
Due to Oxodecanedioic acid's smoothing and conditioning properties, Jamaican black castor oil is ideal for use in products like cleansers, moisturizers, and ethnic hair care products.

Such as:
Polymers
Plasticizers
Lubricants
Corrosion inhibitors

Oxodecanedioic acid has been used in the synthesis of:
biodegradable and elastomeric polyesters [poly(glycerol sebacate)]
novel bio-nylon, PA5.10
novel temperature-response hydrogel based on poly(ether-ester anhydride) nanoparticle for drug-delivery applications

Common Uses for Oxodecanedioic acid:
Sebaceus is Latin for tallow candle, and sebum is Latin for tallow.
These terms refer to the use of Oxodecanedioic acid in the manufacturing of candles.
But as stated above, Oxodecanedioic acid has a lot of uses for the industrial setting.

Oxodecanedioic acid can be used as a monomer for nylon, lubricants, hydraulic fluids, cosmetics, plasticizers and more.
Oxodecanedioic acid can also be used as an intermediate for antiseptics, aromatics and painting products.

Applications of Oxodecanedioic acid:

Major Applications:
Our Oxodecanedioic acid offers a competitve solution in many applications:

To produce polymers:
In industry: to produce plasticizers, lubricants, and corrosion retardants
In cosmetics: as buffering ingredient or as a chemical intermediate to produce a wide range of esters

Cosmetic applications:
Our Oxodecanedioic acid can be used directly in cosmetics formulation as a pH corrector (buffering).
In this case, the main applications are skin care (mainly face/neck care), and color cosmetics.
The Oxodecanedioic acid is also widely used as a synthesis intermediate to produce sebacates esters such as DIPS or DIS (diisopropyl sebacate), DOS (diethylhexyl sebacate), DES (diethyl sebacate) and DBS (dibutyl sebacate).

These sebacate are used as: emollient, solvent, plasticizer, masking (reducing or inhibiting the basic odour of the product), film forming, hair or skin conditioning.
Generally, sebacate esters are claimed to enable a good penetration, give a non-oily and silky skin feel.
These esters are also recognized to be good pigment dispersant (DOS), be good sun protection factor (SPF) booster (DIPS blended), and prevent whitening in antiperspirant (DIPS).

Plasticizers applications:
The Oxodecanedioic acid (DC 10), is widely used to produce a various range of plastics, and brings to those plastics a bio-based part

Case, Metalworking Fluids and Plastics:
Due to Oxodecanedioic acid's smoothing and conditioning properties, Jamaican black castor oil is ideal for use in products like cleansers, moisturizers, and ethnic hair care products.

Lubricants and Greases:
The fatty acids in castor oil give Oxodecanedioic acid excellent lubricating properties.
You can choose either traditional castor oil or Jamaican black castor oil as a lubricant in metal drawing and other industrial processes.

Characteristics of Oxodecanedioic acid:

Acme-Hardesty Oxodecanedioic acid is refined to a minimum 99.5-percent purity.
Oxodecanedioic acid has a minimum acid value of 550, a maximum ash content of 0.03 percent and a maximum moisture level of 0.20 percent.

Oxodecanedioic acid's melting point is between 131.0 and 134.5°C.
Some of the principal uses of Oxodecanedioic acid include acting as an intermediate in nylon, synthetic resins and other plastics.

Oxodecanedioic acid's anti-corrosive properties make it a useful addition to metalworking fluids and antifreezes.
Oxodecanedioic acid is also an additive and thickener for grease and lubricants, as well as an intermediate in paints and other coatings.

Benefits of Oxodecanedioic acid:
In cosmetic products, Oxodecanedioic acid can act as a pH corrector.
In plastics, Oxodecanedioic acid can be used to provide better flexibility and lower melting temperature.

For lubricants and anti-corrosion applications, Oxodecanedioic acid is used to produce a salt derivative that can be used as a coolant for aircraft, automotive and truck engines.

Here are the attributes that make Oxodecanedioic acid as flexible as it is.
Excellent lubricity
Low temperature fluidity
Higher thermal stability
High flash points
Low pour points

Key Benefits:
In cosmetic products, Oxodecanedioic acid can act as a pH corrector.
In plastics, Oxodecanedioic acid can be used to provide better flexibility and lower melting temperature.
For lubricants and anti-corrosion applications, Oxodecanedioic acid is used to produce a salt derivative that can be used as a coolant for aircraft, automotive and truck engines.

The attributes that make Oxodecanedioic acid as flexible as it is:
Excellent lubricity
Low temperature fluidity
Higher thermal stability
High flash points
Low pour points

Alternative Parents of Oxodecanedioic acid:
Dicarboxylic acids and derivatives
Carboxylic acids
Organic oxides
Hydrocarbon derivatives
Carbonyl compounds

Substituents of Oxodecanedioic acid:
Medium-chain fatty acid
Dicarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Compound Type of Oxodecanedioic acid:
Animal Toxin
Cosmetic Toxin
Food Toxin
Industrial/Workplace Toxin
Metabolite
Natural Compound
Organic Compound
Plasticizer

Preparation of Oxodecanedioic acid:
Oxodecanedioic acid is normally made from castor oil, which is essentially glycerol triricinoleate.
The castor oil is heated with sodium hydroxide at about 250°e.

This treatment results in saponification of the castor oil to ricinoleic acid which is then cleaved to give 2-octanol and Oxodecanedioic acid:
This process results in low yields of Oxodecanedioic acid (about 50% based on the castor oil) but, nevertheless, other routes have not proved competitive.
Oxodecanedioic acid is a colourless crystalline solid, m.p. 134℃.

The Main Method of Preparation:
(1) Castor oil is as raw material, ricinoleate is separated from castor oil, with the condition of inflating and 280~300℃, caustic soda proceeds alkali fusion and the reaction is heated for 10h, sebum acid sodium salt can obtain, deputy product is 2-octanol.
The sodium salt is dissolved in water, adding sulfuric acid to neutralize, after bleaching, the solution is cooled to precipitate sebum acid, Oxodecanedioic acid is washed with cold water, and finally recrystallized.

CH3 (CH2) 5CH (OH) CH2CH = CH (CH2) 7COOH +
2NaOH → CH3 (CH2) 5CH (OH) CH3 + NaOOC (CH2) 8COONa + H2
NaOOC (CH2) 3COONa + H2SO4 → HOOC (CH2) 8COOH + Na2SO4

(2) Adipic acid (hexane diacid) is as raw material to synthesize.
Adipic acid and methanol can proceed esterification reaction to form dimethyl adipate, ion exchange membrane proceeds electrolytic oxidation to get dimer, i.e., dimethyl sebacate, and then reacts with sodium hydroxide to form the disodium salt, hydrochloric acid (or sulfuric acid) is used to neutralize and Oxodecanedioic acid can obtain.

Production of Oxodecanedioic acid:
Oxodecanedioic acid is produced from castor oil by cleavage of ricinoleic acid, which is obtained from castor oil.
Octanol & glycerin is a byproduct.
Oxodecanedioic acid can also be obtained from decalin via the tertiary hydroperoxide, which gives cyclodecenone, a precursor to Oxodecanedioic acid.

Oxodecanedioic acid is produced from castor oil by cleavage of ricinoleic acid, which is obtained from castor oil.
Octanol & glycerin is a byproduct.

Oxodecanedioic acid can also be obtained from decalin via the tertiary hydroperoxide, which gives cyclodecenone, a precursor to Oxodecanedioic acid.
Almost all of the current industrial production of Oxodecanedioic acid is using castor oil as raw material.

Castor oil cracking method:
Castor oil is heated under the action of alkali hydrolysis to generate ricinoleic acid sodium soap, and then add sulfuric acid to generate ricinoleic acid; in the presence of diluent cresol, add alkali heated to 260-280 ℃ for cracking to generate Oxodecanedioic acid double sodium salt and secoctanol and hydrogen, cracked material diluted by water, heated and neutralized with acid, the double sodium salt into a monosodium salt; and then boiled with acid after decolorization of activated carbon neutralization solution.
The monosodium salt of Oxodecanedioic acid is turned into Oxodecanedioic acid crystals, and then separated and dried to obtain the finished product.

Potential Medical Significance of Oxodecanedioic acid:
Sebum is a secretion by skin sebaceous glands.
Oxodecanedioic acid is a waxy set of lipids composed of triglycerides (≈41%), wax esters (≈26%), squalene (≈12%), and free fatty acids (≈16%).[4][5]

Included in the free fatty acid secretions in sebum are polyunsaturated fatty acids and Oxodecanedioic acid.
Oxodecanedioic acid is also found in other lipids that coat the skin surface.
Human neutrophils can convert Oxodecanedioic acid to its 5-oxo analog, i.e., 5-oxo-6E,8Z-octadecenoic acid, a structural analog of 5-oxo-eicosatetraenoic acid and like this oxo-eicosatetraenoic acid is an exceptionally potent activator of eosinophils, monocytes, and other pro-inflammatory cells from humans and other species.

This action is mediated by the OXER1 receptor on these cells.
Oxodecanedioic acid is suggested that Oxodecanedioic acid is converted to its 5-oxo analog during, and thereby stimulates pro-inflammatory cells to contribute to the worsening of, various inflammatory skin conditions.

Purification Methods of Oxodecanedioic acid:
Purify Oxodecanedioic acid via the disodium salt which, after crystallisation from boiling water (charcoal), is again converted to the free acid.
The free acid is crystallised repeatedly from hot distilled water or from Me2CO/pet ether and dried under vacuum.

Properties of Oxodecanedioic acid:
Oxodecanedioic acid has high purity.
Oxodecanedioic acid is 100% of vegetal origin.

Oxodecanedioic acid has linear chain.
Oxodecanedioic acid has granules or powder forms.

Oxodecanedioic acid has high reactivity to produce a wide range of esters.
Oxodecanedioic acid Sublimes slowly at 750 mmHg when heated to melting point.

Oxodecanedioic acid is an alpha,omega-dicarboxylic acid that is the 1,8-dicarboxy derivative of octane.
Oxodecanedioic acid has a role as a human metabolite and a plant metabolite.

Oxodecanedioic acid is an alpha,omega-dicarboxylic acid and a dicarboxylic fatty acid.
Oxodecanedioic acid is a conjugate acid of a sebacate(2-) and a sebacate.

Oxodecanedioic acid derives from a hydride of a decane.
Oxodecanedioic acid is a natural product found in Isatis tinctoria, Euglena gracilis, and other organisms with data available.

Handling and Storage of Oxodecanedioic acid:

Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.

Storage class (TRGS 510):
8A: Combustible, corrosive hazardous materials

Stability and Reactivity of Oxodecanedioic acid:

Reactivity:
Oxodecanedioic acid reacts exothermically to neutralize bases, both organic and inorganic.
Oxodecanedioic acid may react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt.

Oxodecanedioic acidan reacts with active metals to form gaseous hydrogen and a metal salt.
Such reactions are slow in the dry, but systems may absorb enough water from the air to allow corrosion of iron, steel, and aluminum parts and containers.

Reacts slowly with cyanide salts to generate gaseous hydrogen cyanide.
Reacts with solutions of cyanides to cause the release of gaseous hydrogen cyanide.

Chemical stability:
Stable under recommended storage conditions.

Incompatible materials:

Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:

Waste treatment methods:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.

Contaminated packaging:
Dispose of as unused product

First Aid Measures of Oxodecanedioic acid:

General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.

Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.

In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures of Oxodecanedioic acid:

Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.

Special hazards arising from the substance or mixture:
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.

Accidental release measures of Oxodecanedioic acid:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Exposure Controls/Personal Protection of Oxodecanedioic acid:

Control parameters:

Components with workplace control parameters:

Contains no substances with occupational exposure limit values.

Exposure controls:

Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:

Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.

Use proper glove removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested: Dermatril (KCL 740 / Aldrich Z677272, Size M)

Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested: Dermatril (KCL 740 / Aldrich Z677272, Size M)

Oxodecanedioic acid should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.

Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).

Control of environmental exposure:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Identifiers of Oxodecanedioic acid:
CAS number, 111-20-6
EC number, 203-845-5
Hill Formula, C₁₀H₁₈O₄
Chemical formula, HOOC(CH₂)₈COOH
Molar Mass, 202.25 g/mol
HS Code, 2917 13 10
Boiling point, 295 °C (133 hPa)
Density, 1.210 g/cm3 (20 °C)
Melting Point, 133 - 137 °C
Vapor pressure, 1 hPa (183 °C)
Bulk density, 600 - 620 kg/m3
Solubility, 1 g/l
Assay (GC, area%), ≥ 98.0 % (a/a)
Melting range (lower value), ≥ 131 °C
Melting range (upper value), ≤ 134 °C
Identity (IR), passes test

PSA: 74.60000
XLogP3: 2.1
Appearance: White powder
Density: 1.231 g/cm3
Melting Point: 130.8 °C
Boiling Point: 294.5 °C
Flash Point: 220 °C
Refractive Index: 1.422
Water Solubility:
Solubility in water, g/100ml: 0.1 (poor)
Storage Conditions:
Storage Room low temperature ventilation drying
Vapor Pressure: 1.24E-06mmHg at 25°C

Properties of Oxodecanedioic acid:
XLogP3: 2.1
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 9
Exact Mass: 202.12050905 g/mol
Monoisotopic Mass: 202.12050905 g/mol
Topological Polar Surface Area: 74.6Ų
Heavy Atom Count: 14
Complexity: 157
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Molecular Weight: 202.25 g/mol
Chemical formula, C10H18O4
Molar mass, 202.250 g•mol−1
Density, 1.209 g/cm3
Melting point, 131 to 134.5 °C (267.8 to 274.1 °F; 404.1 to 407.6 K)
Boiling point, 294.4 °C (561.9 °F; 567.5 K) at 100 mmHg
Solubility in water, 0.25 g/L
Acidity (pKa), 4.720, 5.450

Melting Point, 131°C to 134°C
Density, 1.271
Boiling Point, 295°C (100mmHg)
Flash Point, 220°C (428°F)
Linear Formula, HO2C(CH2)8CO2H
Quantity, 100 g
Beilstein, 1210591
Merck Index, 14,8415
Solubility Information, Slightly soluble in water.
Formula Weight, 202.25
Percent Purity, ≥98%
Chemical Name or Material: Oxodecanedioic acid

Density: 1.1±0.1 g/cm3
Boiling Point: 374.3±0.0 °C at 760 mmHg
Melting Point: 133-137 °C(lit.)
Molecular Formula: C10H18O4
Molecular Weight: 202.247
Flash Point: 198.3±19.7 °C
Exact Mass: 202.120514
PSA: 74.60000
LogP: 1.86
Vapour Pressure: 0.0±1.8 mmHg at 25°C
Index of Refraction: 1.475
Stability: Stable. Combustible. Incompatible with strong oxidizing agents, bases, reducing agents.
Water Solubility: 1 g/L (20 ºC)
OXONE


Oxone (also known as MPS, KMPS, potassium monopersulfate, Potassium peroxymonosulfate, potassium caroate, the trade names Caroat and Oxone, and as a non-chlorine shock in the pool and spa industry) is widely used as an oxidizing agent. It is the potassium salt of peroxymonosulfuric acid. The triple salt 2KHSO5·KHSO4·K2SO4 (known by the trade name Oxone) is a form with higher stability. The standard electrode potential for this compound is 1.81 V with a half-reaction generating the hydrogen sulfate 
Oxone is also used as a wet strength resin paper repulping aid, metal surface treatment agent, selective oxidizer in chemical synthesis, wool shrink proofing treatment, wastewater treatment and odor control agent.

CAS NO: 10058-23-8
EC NO: 233-187-4

IUPAC NAMES: 
Potassium peroxysulfate
potassium;oxido hydrogen sulfate
pentapotassium bis((hydroperoxysulfonyl)oxidanide) hydrogen sulfate sulfate
pentapotassium bis(O-(hydroperoxysulfonyl)oxidanidolate) hydrogen sulfate sulfate
Pentapotassium bis(peroxymonosulphate) bis(sulphate)
pentapotassium bis(peroxymonosulphate) bis(sulphate)
pentapotassium bis(peroxymonosulphate) bis(sulphate)
Potassium peroxymonosulfate
potassium (hydroperoxysulfonyl)oxidanide
Potassium hydrogenperoxomonosulphate
potassium hydrogenperoxomonosulphate
Potassium peroxymonosulphate
potassium peroxymonosulphate


SYNONYMS

potassium hydrogenperoxomonosulphate;Peroxymonosulfuric acid, monopotassium salt;potassium peroxymonosulfuric acid;Kaliumperoxomonosulfat;monopotassium peroxymonosulfurate;Hydroperoxysulfonyloxypotassium;Peroxosulfic acid O-potassium salt;Persulfuric acid hydrogen=potassium salt;Monopotassium peroxymonosulfate;Monopotassium persulfate;Potassium hydrogen peroxomonosulfate;Potassium peroxymonosulfate;ChanGuo potassium hydrogen sulfate;Potassium peroxymonosulfate,>98%;PMPS;POTASSIUM PEROXOMONOSULFATE;POTASSIUM PEROXOMONOSULFATE COMPOUND;POTASSIUM MONOPERSULFATE;POTASSIUM MONOPERSULFATE TRIPLE SALT;POTASSIUM MONOPERSULPHATE TRIPLE SALT;OXONE(TM);OXONE(TM), MONOPERSULFATE;OXONE(TM), MONOPERSULFATE COMPOUND;OXONE;OXONE MONOPERSULFATE COMPOUND;OXONE(R), MONOPERSULFATE COMPOUND;Peroxymonosulfuricacid,monopotassiumsalt,mixturewithdipotassiumsulfateandpotassiumhydrogensulfate;potassiumperoxymonosulfatesulfate,(2khso5.khso4.k2so4);'CARO'S ACID';CAROAT;KMPS;Oxone(4.5% active oxygen);Potassium peroxomonosulfate, min. 4.5% active oxygen, extra pure;Oxone(rg~Potassium peroxymonosulphate;POTASSIUM MONOPERSULFATE TRIPLE SALT, ACTIVE OXGEN CA 4.7% (OXONE);Oxone\(rg~potassium)peroxymonosulfate;Oxone,monopersulfate;Potassium monoperoxysulfate;Potassium peroxymonosulfate sulfate (K5HSO3(O2)2(HSO4)(SO4));POTASSIUMPEROXYMONOSULPHATE;Oxone(R), monopersulfate (Potassium peroxymonosulfate);Potassium Peroxymonosulfate [>45%(T) as KHSO5];Potassium peroxomonosulfate,extra pure,min. 4.5% active oxygen;Oxone, monopersulfate (Potassium peroxymonosulfate);Caro's acid Potassium peroxymonosulfate, Oxone;Potassium Peroxomonosulfate Compound,min4.5% active oxygen;Caros acid, Oxone(R), Potassium peroxymonosulfate;Potassium monopersulphate triple salt, active oxygen ca 4.7%;PotassiuM peroxyMonosulfate sulfate (K5(HSO5)2(HSO4)(SO4));oxido hydrogen sulfate;tetrapotassium;Potassium Peroxymonosulfate [> ca. 45%(T) as KHSO5];PotassiuM peroxoMonosulfate, 4.5% active oxygen;Potassium peroxymonosulfonate;Potassium peroxomonosulfate, for synthesis, 4.5% active oxygen;PotassiumPeroxomonosulphate(Oxone);Potassium peroxymonosulfate,Active Oxygen≥4.5%;Potassium hydrogen monopersulfate;Potassium peroxymonosulfate joyce;OXONE, MONOPERSULFATE COMPOUNDOXONE, MONOPERSULFATE;COMPOUNDOXONE, MONOPERSULFATE COMPOUND;Potassiumhydrogenperoxymonosulfate;PotassiuM 3-sulfotrioxidan-1-ide;PotassiuM Monopersulfate coMpound;Oxone , potassium monopersulfate;potassium peroxymonopersulfate;Oxone|r, Monopersulfate;Potassium monoperoxysulfate OXONE(R);POTASSIUM HYDROGEN MONOPERSULFATE FOR SY;PotassiuM peroxyMonosulfate,Monopersulfate coMpound;Potassium monoperoxysulfate OXONE;Potassium PeroxomonosuL;Potassium peroxymonosulfate triple salt;Potassium monopersulfate (Oxone);Potassium hydrogen monopersulfate for synthesis;potassiumperoxymonosulfatesulfate(k5h3(so3(o2))2(so4)2);PotassiumMonopersulphate,ActiveComponent42%Min;Potassium Monopersulphate, Active Component 42%Min, Cas;Potassium peroxymonosulfate sulfate (K5HSO3(O2)SO3(O2)(HSO4)2);CAROAT (POTASSIUM MONOPERSULFATE);Pentakalium-bis(peroxymonosulfat)-bis(sulfat);Potassium Monopersulfate Sulfate;Pentapotassium bis(peroxymonosulphate) bis(sulphate);Potassium peroxymonosulfate;Potassium peroxymonosulfate sulfate;POTASSIUM CAROATE;Oxone PS-16;Potassium monopersulfate triple salt,42.8-46%;Potassium peroxymonosulfat;Potassium perbisulfate;Potassiummonopersulfatetriplesal;10058-23-8;Potassium hydrogen dioxidan-2-idesulfonate (1:1:1);POTASSIUM PEROXOSULFATE;Potassium sulfodioxidanide;Sulfodioxidanide de potassium;potassium (hydroperoxysulfonyl)oxidanide;dipotassium dioxidan-2-idesulfonate
37222-66-5;Potassium Peroxomonosulfate;Potassium monopersulfate triple salt;MFCD00040551;Oxone, monopersulfate;DTXSID8051415,OXONE(R), monopersulfate compound;AKOS015912003;AKOS030228420;SC-26713;FT-0697154;O0310;Potassium monopersulfate triple salt, >=47% KHSO5 basis;pentapotassium;hydrogen sulfate;oxido hydrogen sulfate;sulfate

What is Oxone?
Oxone is an inorganic chemical compound. It is primarily used for the treatment of wastewater. Potassium monopersulfate occurs as white crystals or powder with hygroscopic properties.
Oxone is exceedingly hygroscopic and is readily soluble in water to form the monopersulfate salts.
It has very low solubility in organic solvents, but excellent solubility in acids and aqueous solutions of acids and bases.
Oxone is known for its ability to convert hypochlorite ion into free chlorine. It also produces free chlorine without oxidizing ammonia.
Oxonee can be used to control pH fluctuations in water treatment systems.
Potassium monopersulfate for swimming pools. Potassium monopersulfate is frequently used by swimming pool owners to make chlorination water.
Potassium monopersulfate is also used to treat industrial wastewater.
In swimming pools, it is an effective oxidizer for controlling algae. It also helps prevent the formation of precipitates that can cloud the water.

Benefits of Oxone
The benefits of Oxone include reducing phosphates and chemical use, stabilizing pH in a pool, eliminating algae. It also increases circulation, which saves energy. As a result, pools using Oxone have increased clarity, and decreases the likelihood of chemical and odor problems. 
Oxone is not the same as the Chlorine you are used to using. Discretely, Oxone is similar to bleach, but it is not a typical bleach product. To determine advantages in your pool, you must first understand the chemical formula. Because Oxone is a salt, it has a chemical formula containing Potassium. Other ingredients, such as Oxygen, and Sulfur (Sulfur is the "E" in Oxone) are added. Using this formula, the official chemical name for Oxone is Potassium Peroxymonosulfate, and if was not derived from bleach, it would be considered a bleach product.


Reactions
MPS is a versatile oxidant. It oxidizes aldehydes to carboxylic acids; in the presence of alcoholic solvents, the esters may be obtained. Internal alkenes may be cleaved to two carboxylic acids (see below), while terminal alkenes may be epoxidized. Sulfides give sulfones, tertiary amines give amine oxides, and phosphines give phosphine oxides.
Illustrative of the oxidative power of this salt is the conversion of an acridine derivative to the corresponding acridine-N-oxide.

MPS will also oxidize sulfide to a sulfone with 2 equivalents. With one equivalent the reaction converting sulfide to sulfoxide is much faster than that of sulfoxide to sulfone, so the reaction can conveniently be stopped at that stage if so desired.

MPS can also react with ketones to form dioxiranes, with the synthesis of dimethyldioxirane (DMDO) being representative. These are versatile oxidising agents and may be used for the epoxidation of olefins. In particular, if the starting ketone is chiral then the epoxide may be generated enantioselectively, which forms the basis of the Shi epoxidation.

Uses
Swimming Pools
Oxone can be used in swimming pools to keep the water clear, thus allowing chlorine in pools to work to sanitize the water rather than clarify the water, resulting in less chlorine needed to keep pools clean. One of the drawbacks of using Oxone in pools is it can cause the common DPD #3 water test for combined chlorine to read incorrectly high. Moreover, by-products can be formed during the peroxymonosulfate treatment, which are sometimes even more toxic than the original contaminants.

The composition of the oxidizing agent Oxone is 2KHSO5.KHSO4.K2SO4. The active component potassium monopersulfate (KHSO5, potassium peroxomonosulfate) is a salt from the Caro´s acid H2SO5.

The use of Oxone has increased rapidly. Reasons for this are the stability, the simple handling, the non-toxic nature, the versatility of the reagent and the low costs.

As long as Oxone is stored under dry and cool conditions, it loses about 1% activity per month under release of oxygen and heat. Decomposition to SO2 and SO3 takes place under the influence of heat (starting at 300°C). 

Acidic, aqueous solutions of the pure reagent in distilled water are relatively stable. The stability reaches a minimum at pH 9, where the mono anion (HSO5-) has the same concentration as the dianion (SO52-). Iron, cobalt, nickel, copper, manganese and further transition metals can catalyze the decay of Oxone in solution.

The following secondary reactions should be avoided: 
Halides can be oxidized to halogens (e.g. chloride to chlorine), cyanides react with Oxone under release of hydrogen cyanide, "heavy" transition metals (Cu, Mn, Co, Ni) and their salts lead to the decomposition of Oxone under release of oxygen.

Whenever strong oxidation is needed Oxone monopersulfate compound is the right choice for a wide variety of industrial and consumer applications.

Also known as KPMS or potassium peroxymonosulfate, Oxon is a white granular product that provides non-chlorinated oxidation in a wide variety of applications. It's safe to use in a production facility, in the environment, and even as a key ingredient in your denture cleaner!

Most notably, the active ingredient allows for efficient non-chlorinated oxidation as a pool shock, allowing less use of sanitizer and leaves the pool clean, clear, and swimmable nearly immediately. The powerful oxidation as a microetchant in printed circuit boards improves process control in multi-step copper etching with a predictable rate to completion. KPMS is of particular interest in metal plating and mining as it safely, economically, and conveniently oxidizes cyanide in waste streams. These key benefits of rapid rate of reaction as well as non-chlorinated oxidation has allowe repulping papers with wet strength resins to move their processes to greener methods without sacrificing production time.

Oxone monopersulfate compound is a white, granular, freeflowing peroxygen that provides powerful non-chlorine oxidation for a wide variety of industrial and consumer uses.

Application areas:

• Swimming pool shock oxidizer
• Printed wiring board microetchant
• Repulping aid for wet-strength-resin destruction
• Odor control agent in wastewater treatment
• Bleach component in denture cleanser and laundry formulations
• Activator in antimicrobial compositions
• Other uses where its combination of powerful oxidation and relative safe handling properties are of value 

The active ingredient of Oxone, commonly known as potassium monopersulfate, which is present as a component of a triple salt with the formula 2KHSO5·KHSO4·K2SO4 potassium hydrogen peroxymonosulfate sulfate The oxidizing power of Oxone is derived from its peracid chemistry; it is the first neutralization salt of peroxymonosulfuric acid H2SO5.

Stability
Oxone is a very stable peroxygen in the solid state and loses less than 0.5% (relative) of its activity per month when stored under recommended conditions. However, like all other peroxygens, Oxone undergoes very slow disproportionation with the liberation of heat and oxygen gas. If a decomposition is associated with high temperature, decomposition of the constituent salts of Oxone may generate sulfuric acid, sulfur dioxide, or sulfur trioxide.
The stability is reduced by the presence of small amounts of moisture, alkaline chemicals, chemicals that contain water of hydration, transition metals in any form, and/or any material with which Oxone can react. Since the decomposition of Oxone is exothermic, the decomposition can self-accelerate if storage conditions allow the product temperature to rise.

The stability is adversely affected by higher pH, especially above pH 7. A point of minimum stability exists at about pH 9, at which the concentration of the mono-anion HSO5 - is equal to that of the. Cobalt, nickel, and manganese are particularly strong catalysts for the decomposition of Oxon in solution; the degree to which catalysis occurs is dependent on the concentrations of Oxone and of the metal ion. 

Product Grades
Oxone is available in both granular and liquid forms. By screening, grinding, or compaction/granulation processing, several granular grades are produced which differ in particle size distribution. Liquid products are specially-formulated to optimize active oxygen stability. 

Solubility
Oxone is highly and readily soluble in water. At 20°C (68°F), the solubility of Oxone in water is >250 g/L. At concentrations above saturation, potassium sulfate will precipitate, but an additional active component, Oxone, will remain in the solution.

Oxone is also called MPS, or Potassium Monopersulfate. MPS does not contain chlorine, as it is a potassium salt of peroxymonosulfuric acid.

Oxone is marketed as a popular non-chlorine based shock. Its primary swimming pool use is to oxidize any contaminants in the water, leaving chlorine or bromine sanitizers already present in the water to focus on sanitizing the water.

There are several advantages of using Oxone in swimming pools:

Since there is no chlorine added, the swimming pool is available for swimming immediately after the shock has dissolved and time has been given for the oxidation process to complete. Oxidation is usually complete in about one to two hours, versus eight or more hours for chlorine-based shock.
Chlorine use can decrease, as less chlorine is needed to oxidize organic and inorganic matter in the pool.
There are several disadvantage of using Oxone as a shock treatment in swimming pools

Chlorine tests can read incorrectly high in DPD or FAS-DPD tests, as the non-chlorine shock may show up as combined chlorine in these tests.
More expensive than chlorine-based shock products.
If adequate chlorine sanitizer levels are not maintained, then adding non-chlorine shock like MSP may increase the risk of algae growth due to possible nitrate creation from adding MPS.

Chemical Properties
white crystalline powder

Uses
PCB metal surface treatment chemical and water treatment etc.

Purification Methods
This is a stable form of Caro's acid and should contain >4.7% of active oxygen. It can be used in EtOH/H2O and EtOH/AcOH/H2O solutions. If active oxygen is too low. it is best to prepare it afresh from 1mole of KHSO5, 0.5mole of KHSO4 and 0.5mole of K2SO4. 

Used for oral cavity cleaning, swimming pool and hot spring water disinfection, pulp bleaching

1. Disinfection of family living environment 
Novel coronavirus can be rapidly killed by 1:100 dilution
1:400 dilution can kill H5N1 avian influenza virus
Can kill common bacteria, fungi, viruses (influenza virus Noah virus)
It is used for washing hands and disinfecting, spraying the floor of hotels, dining halls, vehicles, colleges and cinemas, and disinfecting the walls and other crowded places

2. Disinfection of animal breeding environment
African swine fever can be killed by 1:400 dilution for 1min
Disinfect and deodorize, improve air quality

3. Low temperature cold chain disinfection
The antifreeze spray can be sterilized at minus 18 degrees Celsius and minus 40 degrees Celsius by adding the diluted water solution of antifreeze

4. Repair damaged soil, improve river environment, sewage treatment, aquaculture, etc

Product Functions Applications:

Active indication: This product's aqueous solution oxidation state is pink, the reduced state is colorless, easy for users to judge the effectiveness of a disinfectant, avoid ineffective disinfection.Multi-function, multi-purpose:
Applicable to a variety of places disinfection: can be used for farm office, pet operating room, clinic room, canteen, dormitory and other disinfection.
Suitable for disinfection of various methods: can be used for environment, clothing, rubber boots, water supply system, equipment, apparatus, washbasin disinfection.
One operation, multiple harvests: in the disinfection process, it can effectively reduce the odor and improve the air quality while suppressing and killing the pathogenic microorganisms.

When chlorine is used to oxidize pool water, it reacts with bather and other organic wastes, which are primarily nitrogen-based compounds, to form chloramines. These by-products have a foul odor and are considered unpleasant. Oxone also reacts with the nitrogen-based compounds introduced by bathers, but because it does not contain chlorine, it does not form chloramines in its oxidation process. 

Actually, It reacts very slowly with ammonia. Oxone's lifetime in pool water depends on the quantity of oxidizable material. All things being equal, however, it is not nearly as sensitive to sunlight as chlorine. Unstabilized chlorine is more than 90 percent decomposed within a few hours, while Oxone is about 23 percent decomposed per hour, according to Wojtowitc.

One of its greatest advantages is that bathers can reenter the water a short time after it has been added — typically about 30 minutes.

Oxone dissolves quickly and does not fade liners. It works well with chlorine, arguably allowing chlorine to work more efficiently as a sanitizer. Using Oxone is highly recommended for indoor pools, where there is no sunlight or wind to help break down and carry away combined chlorine. For indoor pools, shocking with Oxone is recommended about once a week.

The active ingredient allows for efficient non-chlorinated oxidation as a pool shock, allowing less use of sanitizer and leaves the pool clean, clear, and swimmable nearly immediately. The powerful oxidation as a micro etchant in printed circuit boards improves process control in multi-step copper etching with a predictable rate to completion. 
Oxone is of particular interest in metal plating and mining as it safely, economically, and conveniently oxidizes cyanide in waste streams. These key benefits of the rapid rate of reaction as well as non-chlorinated oxidation allow repulping papers with wet strength resins to move their processes to greener methods without sacrificing production time.

Overview

Oxone is a non-chlorine oxidizer and is used as an oxidizing agent in the pool and spa industry. The active ingredients of Oxone are potassium sulfate, potassium monopersulfate, and potassium bisulfide. Oxone is popularly known by its trade names such as Oxone, Caroat, and non-chlorine shock. Oxone has a similar magnitude of oxidation potential as chlorine and does not form chloramines during its oxidation process. In addition, it is highly soluble in water and provides high microbiological effectiveness and powerful non-chlorine oxidation for various industrial applications. Oxone is widely used as a disinfectant in wastewater treatment, swimming pools, etc., for reducing the organic and microbe content of the water. It is used as a cleaning agent in printed circuit boards, as an oxidizer agent for treating wool, and as an auxiliary agent for organic chemicals. In addition, it finds application in paper recycling, carpet browning, and oral hygiene formulations.
Oxone offers low shrink resistance during the wool as well as laundry bleaching processes.
Oxone aids in the quick cleaning of pools and leads to less usage of sanitizer due to its strong non-chlorinated oxidation potential. 

Application Areas

•Oxone is used in the formulations of Denture cleaners. Oxone is the effective main ingredient in Cleaning tablets for dentures.
•Oxone is used in disinfectants: Oxone is suitable for use for chlorine-free disinfection or purification of swimming pool water and spas.
•Prevention of chlorine acne and eye irritation.
•Approved for oxidative drinking water treatment.
•Oxone is a bleaching agent: Oxone has a bleaching effect comparable to that of organic peracids
•Oxone has a biocidal effect: Oxone is suitable as an additive to acidic cleaning agents with bleaching and disinfectant effect.
•Oxone works very well in effluent treatment: Oxidative treatment of problematic effluents; sulfide oxidation, nitrite oxidation, and cyanide detoxification.
•Plaster additive: The addition of Oxone leads to the generation of oxygen and improved product characteristics (e.g. thermal insulation, water absorbency, mechanical properties).
•Metal treatment: Micro Etchant: Oxone is used for etching printed circuit boards.

•Odor control agent
•Paper industry
•Pulp and paper recycling
•Professional Disinfection
•Personal Care
•Pool & Spa
•Pool & Spa Shock Oxidizer
•Pulp & paper repulping aid
•rendering plants
•Laundry Bleach Ingredient
•Material protection
•Selective oxidizer in chemical synthesis
•Food industry
•Chemical Industry
•Disinfection of drinking water
•Denture cleanser bleach additive
•Disinfection
•Effluent treatment agent
•Electronics Industry
•Surface Treatment (electronic industry)
•Waste water treatment agent
•Textile industry
•Wool treatment
•Washing- and cleaning agent industry
•Wastewater treatment
•Water Treatment
•Metal surface treatment
•Laundry
•Animal Hygiene
•Chemical synthesis
•Cosmetics


Treatment efficiency of Oxone compound, a new kind of oxidation reagent, on killing algae and bacteria and the effect of influence factors, such as dosage, contact time and temperature are also discussed. Oxone appropriate for killing algae and bacteria in landscape water, dosage and contact time are the major influence factors. The contact time should be longer than 20min and the algicidal rate is higher when the temperature is above 20°C.

The appropriate usage of disinfectants is critical for establishing a successful sanitation program. Because not all disinfectants are effective against major pathogens, different families of disinfectants that target specific microorganisms should be considered. For instance, several bacteria and viruses are sensitive to phenols; however, most bacteria are also sensitive to quaternary ammonium, iodophors, paracetic acid, glutaraldehydes, and cresols. Therefore, there is no single disinfectant reported in the literature that would be efficacious against a wide spectrum of etiological agents that economically impact diseases in animal farms. 

Oxone is the potassium salt of peroxymonosulfuric acid, which is widely used as an oxidizing agent. 
Oxone , contain potassium monopersulfate for their main ingredient, as a non-chlorine shock agent; Oxone breaks the chlorine–ammonia bond formed when chlorine combines with ammonia, without increasing the chlorine level of the swimming pool; hence, Oxone can be used in swimming pools to keep the water clear. 

Generally, bacteria and viruses are highly resistant to disinfectants contained in bio-environmental constituents such as feces, saliva, or vomitus.
Oxone can inactivate bacteria and viruses either in the absence or presence of organic materials, and it is useful as an alternative disinfectant, especially for biosecurity enhancement aiming to control bacteria and viruses that contaminate animal farms and hospitals.
The most popular sanitizers used in pools and spas—chlorine and bromine—function both as biocides (they kill bacteria and other potentially harmful microbes) and oxidizers (they "burn up" unpleasant organic contaminants like bather wastes, dust, and pollen). 
The periodic addition of a supplemental oxidizer—a "shock treatment"—can free up the sanitizer for its highest purpose, killing germs. 

Potassium monopersulfate is a powerful oxidizer with several attractive properties.
Properly applied, it will prevent the formation of new combined chlorine by eliminating organics in the water without creating more combined chlorine. Bathers can re-enter the water after waiting a short period of time (usually one hour) to allow proper mixing and circulation. The reaction byproducts are harmless sulfate salts.

After traditional shocking, then use the Oxone product to prevent further combined chlorine development.

Oxone products are particularly useful in indoor environments where proper air exchange rates may be nonexistent. Monopersulfate does not cause odors or irritation. 

OXONE
OXONEPotassium peroxymonosulfate (also known as MPS, KMPS, potassium monopersulfate, potassium caroate, the trade names Caroat and Oxone, and as non-chlorine shock in the pool and spa industry[2][3][4]) is widely used as an oxidizing agent. It is the potassium salt of peroxymonosulfuric acid.The triple salt 2KHSO5·KHSO4·K2SO4 (known by the tradename Oxone) is a form with higher stability.[5] The standard electrode potential for this compound is +1.81 V with a half reaction generating the hydrogen sulfate (pH=0).[6]HSO5− + 2 H+ + 2 e− → HSO4− + H2OReactionsMPS is a versatile oxidant. It oxidizes aldehydes to carboxylic acids; in the presence of alcoholic solvents, the esters may be obtained.[7] Internal alkenes may be cleaved to two carboxylic acids (see below), while terminal alkenes may be epoxidized. Sulfides give sulfones, tertiary amines give amine oxides, and phosphines give phosphine oxides.Illustrative of the oxidative power of this salt is the conversion of an acridine derivative to the corresponding acridine-N-oxide.[8]Acridine oxidation by oxone, standardized.pngMPS will also oxidize a sulfide to a sulfone with 2 equivalents.[9] With one equivalent the reaction converting sulfide to sulfoxide is much faster than that of sulfoxide to sulfone, so the reaction can conveniently be stopped at that stage if so desired.Oxidation of an oragnic sulfide by oxone.pngMPS can also react with ketones to form dioxiranes, with the synthesis of dimethyldioxirane (DMDO) being representative. These are versatile oxidising agents and may be used for the epoxidation of olefins. In particular, if the starting ketone is chiral then the epoxide may be generated enantioselectively, which forms the basis of the Shi epoxidation.[10]The Shi epoxidationUsesSwimming PoolsOxone can be used in swimming pools to keep the water clear, thus allowing chlorine in pools to work to sanitize the water rather than clarify the water, resulting in less chlorine needed to keep pools clean.[11] One of the drawbacks of using Oxone in pools is it can cause the common DPD #3 water test for combined chlorine to read incorrectly high.[12] Moreover, byproducts can be formed during the peroxymonosulfate treatment, which are sometimes even more toxic than the original contaminants.[13]Laboratory DisinfectionOxone is the main active ingredient in Virkon, which is used for disinfection of laboratory equipment.OxoneKHSO5.pngNamesIUPAC namePotassium peroxysulfateOther namesCaroatOxonepotassium monopersulfateMPSIdentifiersCAS Number 10058-23-8 ☒37222-66-5 (triple salt, see text) ☒3D model (JSmol) Interactive imageChemSpider 8053100 ☒ECHA InfoCard 100.030.158 Edit this at WikidataPubChem CID 11804954PropertiesChemical formula KHSO5Molar mass 152.2 g/mol (614.76 as triple salt)Appearance off-white powderSolubility in water decomposesOxone, Potassium peroxomonosulfateThe composition of the oxidizing agent Oxone® is 2KHSO5.KHSO4.K2SO4. The active component potassium monopersulfate (KHSO5, potassium peroxomonosulfate) is a salt from the Caro´s acid H2SO5.The use of Oxone has increased rapidly. Reasons for this are the stability, the simple handling, the non-toxic nature, the versatility of the reagent and the low costs.As long as Oxone is stored under dry and cool conditions, it loses about 1% activity per month under release of oxygen and heat. Decomposition to SO2 and SO3 takes place under the influence of heat (starting at 300°C). Acidic, aqueous solutions of the pure reagent in distilled water are relatively stable. The stability reaches a minimum at pH 9, where the mono anion (HSO5-) has the same concentration as the dianion (SO52-). Iron, cobalt, nickel, copper, manganese and further transition metals can catalyze the decay of Oxone in solution.The following secondary reactions should be avoided: Halides can be oxidized to halogens (e.g. chloride to chlorine), cyanides react with Oxone under release of hydrogen cyanide, "heavy" transition metals (Cu, Mn, Co, Ni) and their salts lead to the decomposition of Oxone under release of oxygen.OXONE™ MONOPERSULFATE COMPOUNDWhenever strong oxidation is needed Oxone™ monopersulfate compound is the right choice for a wide variety of industrial and consumer applications.Oxone™ is available in both granular and liquid forms. By screening, grinding, or compaction/granulation processing, several granular grades (Regular, PS16, and CG) are produced which differ in particle size distribution. Liquid products are specially formulated to optimize active oxygen stability.Oxone®Monopersulfate CompoundGENERAL TECHNICAL ATTRIBUTESOxone® monopersulfate compound is a white, granular, freeflowing peroxygen that provides powerful non-chlorine oxidation for a widevariety of industrial and consumer uses.Applications• Swimming pool shock oxidizer• Printed wiring board microetchant• Repulping aid for wet-strength-resin destruction• Odor control agent in wastewater treatment• Bleach component in denture cleanser and laundry formulations• Activator in antimicrobial compositions• Other uses where its combination of powerful oxidation and relativesafe handling properties are of valueThe active ingredient of Oxone® is potassium peroxymonosulfate, KHSO5(CAS 10058-23-8), commonly known as potassium monopersulfate,which is present as a component of a triple salt with the formula2KHSO5·KHSO4·K2SO4 potassium hydrogen peroxymonosulfate sulfate(5:3:2:2), [CAS 70693-62-8]).The oxidizing power of Oxone® is derived from its peracid chemistry; it isthe first neutralization salt of peroxymonosulfuric acid H2SO5 (also knownas Caro’s acid).Standard PotentialThe standard electrode potential (E°) of KHSO5 is given by the followinghalf cell reaction:The thermodynamic potential is high enough for many room temperatureoxidations including:• Halide to active halogen• Oxidation of reduced sulfur and nitrogen compounds• Cyanide to cyanate• Epoxidation of olefins• Baeyer-Villigar oxidation of ketones• Copper metal to cupric ion• Ferrous to ferric ion• Manganous to manganic ionStabilityOxone® is a very stable peroxygen in the solid stateand loses less than 0.5% (relative) of its activity per month when stored under recommended conditions. However, like all other peroxygens, Oxone® undergoes very slow disproportionation with the liberation of heat and oxygen gas. If a decomposition is associated with high temperature, decomposition of the constituent salts of Oxone® may generate sulfuric acid, sulfurdioxide, or sulfur trioxide. The stability is reduced by the presence of small amounts of moisture, alkaline chemicals, chemicals that contain water of hydration, transition metals in any form, and/or any material with which Oxone® can react. Since the decomposition of Oxone® is exothermic, the decomposition can self-accelerate if storage conditions allow the product temperature to rise.Product GradesOxone® is available in both granular and liquid forms. Byscreening, grinding, or compaction/granulation processing, several granular grades (Regular, PS16, and CG) are produced which differ in particle size distribution (Table 3). Liquid products are specially-formulated to optimize active oxygen stability.Oxone PS-16Oxone PS-16 known as KPMS or potassium peroxymonosulfate. Oxone is a white granular product that provides non-chlorinated oxidation in a wide variety of applications such as: industrial processing, pulp and paper production, waste water treatment, industrial and household cleaning, oil and gas production, and denture cleaning.Product OverviewOxone PS-16 made provides a green method for industrial and consumer oxidation needs. Oxone™ PS-16 is a non-chlorinated solution to oxidation needs and is highly stable and easy to use in solution.Product SpecificationsTriple salt molecular weight: 614.7Active oxygen min: 4.5%Active oxygen typical analysis: 4.7%Active oxygen theoretical: 5.2%Active component: KHSO5KHSO5 min: 42.8%KHSO5 typical: 44.7pH, at 25°C of 1% solution: 2.3pH, at 25°C of 3% solution: 2.0Primary Chemistry: Potassium Monoper-Sulfate, KHSO5Features & BenefitsNon-chlorinate oxidizer in free flowing solid form.High water solubility at ambient temperatures.Solution stability (even under acidic conditions).Low toxicity when compared to chlorinated. options and other oxidizers.No oxidizer label required.Highly predictable etch rate for production of micro electronics.Problems SolvedChlorinated oxidizers are not desired. Looking for a greener and easier to handle oxidizing agentScale formation and white precipitation caused by calcium hypochlorites and solid form oxidizersOxidizer label required with the use of bleach in formulationsLimited to no control over etching rate in the production of electronics and microelectronicsPool turns dark or green due to algae bloomHigh level of free and combined chlorine in pool and spa applicationsFrequent cleaning or replacement of paper mill felts is required or of felts in paper millsInsufficient bleaching in denture cleansers, textiles, and cleaning applicationsPool & Spa shock treatmentPrinted circuit board microetchantRepulping aid for wet-strength resin destructionOxidizing agent for Felt WashOdor control agent in wastewater treatmentCyanide destruction in miningBleach functionality for denture cleanser, textiles, and cleaning applicationsActive ingredient for disinfection applicationsMolecular Weight of Oxone: 614.8 g/mol Computed by PubChem 2.1 (PubChem release 2019.06.18)Hydrogen Bond Donor Count of Oxone: 3 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)Hydrogen Bond Acceptor Count of Oxone: 18 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)Rotatable Bond Count of Oxone: 0 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)Exact Mass of Oxone: 613.638755 g/mol Computed by PubChem 2.1 (PubChem release 2019.06.18)Monoisotopic Mass of Oxone: 613.638755 g/mol Computed by PubChem 2.1 (PubChem release 2019.06.18)Topological Polar Surface Area of Oxone: 365 Ų Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)Heavy Atom Count of Oxone: 27 Computed by PubChemFormal Charge of Oxone: 0 Computed by PubChemComplexity of Oxone: 239 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)Isotope Atom Count of Oxone: 0 Computed by PubChemDefined Atom Stereocenter Count of Oxone: 0 Computed by PubChemUndefined Atom Stereocenter Count of Oxone: 0 Computed by PubChemDefined Bond Stereocenter Count of Oxone: 0 Computed by PubChemUndefined Bond Stereocenter Count of Oxone: 0 Computed by PubChemCovalently-Bonded Unit Count of Oxone: 9 Computed by PubChemCompound of Oxone Is Canonicalized Yes
OXONE
Oxone is a white, odourless, crystalline, free-flowing solid powder.
Oxone is a white powder and non-chlorine oxidizer, whose chemical formula is 2KHSO5·KHSO4·K2SO4.


CAS Number: 70693-62-8
EC Number: 274-778-7
MDL Number: MFCD00040551
Molecular Fomula: 2KHSO5·KHSO4·K2SO4



Potassium peroxysulfate, Caroat, Oxone Potassium monopersulfate, potassium monopersulfate, MPS, KMPS, potassium caroate, non-chlorine shock, Potassium peroxymonosulfate sulfate, PotassiuM Monopersulfate coMpound, potassium peroxymonopersulfate, PotassiuM 3-sulfotrioxidan-1-ide, Potassium hydrogen monopersulfate, Potassiumhydrogenperoxymonosulfate, Potassium peroxymonosulfate,Active Oxygen≥4.5%, Oxone Potassium monopersulfate PS-16, OXONE POTASSIUM MONOPERSULFATE Extra Pure, POTASSIUM CAROATE, Oxone Potassium monopersulfate, Potassium Monopersulfate, Potassium peroxymonosulfate, Oxone Potassium monopersulfate, potassium monopersulfate, PotassiuM 3-sulfotrioxidan-1-ide, potassium 3-sulfotrioxidan-1-ide, Potassium hydrogen monopersulfate, PotassiuM Monopersulfate coMpound, Potassium peroxymonosulfate joyce, Potassiumhydrogenperoxymonosulfate, Potassium hydrogen peroxymonosulfate, OXONE POTASSIUM MONOPERSULFATE, MONOPERSULFATE COMPOUNDOXONE POTASSIUM MONOPERSULFATE, MONOPERSULFATE COMPOUNDOXONE POTASSIUM MONOPERSULFATE, MONOPERSULFATE COMPOUND, Potassium peroxymonosulfate, Potassium monopersulfate, Potassium monoperoxysulfate, Potassium hydrogen persulfate, Oxone Potassium monopersulfate, Potassium Monopersulfate, Potassium peroxymonosulfate, Oxone Potassium monopersulfate , potassium monopersulfate, PotassiuM 3-sulfotrioxidan-1-ide, potassium 3-sulfotrioxidan-1-ide, Potassium hydrogen monopersulfate, PotassiuM Monopersulfate coMpound, Potassium peroxymonosulfate joyce, Potassiumhydrogenperoxymonosulfate, Potassium hydrogen peroxymonosulfate, OXONE POTASSIUM MONOPERSULFATE, MONOPERSULFATE COMPOUNDOXONE POTASSIUM MONOPERSULFATE, MONOPERSULFATE COMPOUNDOXONE POTASSIUM MONOPERSULFATE, MONOPERSULFATE COMPOUND, KMP, PMPS, Potassium peroxymonosulphate, Potassium hydrogen monopersulphate, Potassium monopersulphate triple salt, Potassium peroxymonosulfate, potassium monopersulfate compound, Potassium hydrogen sulfate, PMPS, KMPS,




Oxone is a white, granular, free-flowing peroxygen powder that provides powerful non-chloride oxidation.
Oxone is the potassium salt of peroxymonosulfuric acid.
The active ingredient of Oxone is present as a component of a triple salt with the formula 2KHSO5·KHSO4·K2SO4 [potassium hydrogen peroxymonosulfate sulfate, [CAS-RN 70693-62-8].


The oxidation potential of Oxone is derived from its peracid chemistry; it is the first neutralization salt of peroxymonosulfuric acid H2SO5 (also known as Caro's acid).
Oxone is a highly active oxidant that is very effective at disinfecting swimming pools and lagoons.


Oxone's oxidation potential exceeds even that of hydrogen peroxide and ozone.
Oxone is an odourless white powder that dissolves easily in water, sanitizing and improving water clarity without the carcinogenic trihalomethanes (THMs) that chlorine produces.


Oxone is ANSI60 certified for drinking water applications.
Oxone is abbreviated as PMs, which is a convenient, stable, and widely used inorganic acidic oxidant and disinfectant.
Oxone has strong non-chlorine oxidation ability, the product is safe and stable in solid state, easy to store, safe and convenient to use.


Oxone is a substance that can rapidly oxidize swimming pool .
Oxone is also called MPS, or Potassium peroxymonosulfate, as it is a potassium salt of peroxymonosulfuric acid.
Oxone is marketed as a popular non-chlorine based shock.


Oxone's primary swimming pool use is to oxidize any contaminates in the water, sanitizers already present in the water to focus on sanitizing the water.
Oxone is the first raw material verified for removal of wet strength resins in paper repulping.
Oxone is chlorine-free, meaning chlorine can be eliminated from the repulping process.


Oxone is extra pure an oxidizing agent.
Oxone is the potassium salt of peroxymonosulfuric acid.
Oxone is a white, odourless, crystalline, free-flowing solid powder.


Oxone decomposes when the temperature exceeds 60 degrees.
Oxone is highly soluble in water and slightly corrosive.
Oxone provides powerful non-chlorine oxidation and microbiological effectiveness for various industrial and consumer uses.


Oxone has the advantage of being highly stable in storage, easy and safe to handle.
Oxone complex is an inorganic acidic oxidant, also known as potassium monopersulfate complex salt, potassium persulfate triplex salt peroxide potassium sulfate salt, is the common functional chemicals Oxone, Caroat, ZA200/100, Basolan2448 basic effective components.


Oxone, is a substance that can rapidly oxidize swimming pool .
Oxone is also called MPS, or Potassium peroxymonosulfate, as it is a potassium salt of peroxymonosulfuric acid.
Oxone is marketed as a popular non-chlorine based shock.


Its primary swimming pool use is to oxidize any contaminates in the water, sanitizers already present in the water to focus on sanitizing the water.
Oxone does not contain chlorine, as it is a potassium salt of peroxymonosulfuric acid.
Oxone is marketed as a popular non-chlorine based shock.


Oxone's primary swimming pool use is to oxidize any contaminates in the water, leaving chlorine or bromine sanitizers already present in the water to focus on sanitizing the water.
Oxone is widely used as an oxidizing agent, for example, in pools and spas (usually referred to as monopersulfate or "MPS").


Oxone is the potassium salt of peroxymonosulfuric acid.
Oxone is a relatively obscure salt, but its derivative called oxone is of commercial value.
Oxone refers to the triple salt 2KHSO5·KHSO4·K2SO4.


Oxone has a longer shelflife than does potassium peroxymonosulfate.
A white, water-soluble solid, Oxone loses <1% of its oxidizing power per month.
Oxone converts ketones to dioxiranes.


The synthesis of dimethyldioxirane (DMDO) from acetone is representative.
Dioxiranes are versatile oxidising agents and may be used for the epoxidation of olefins.
In particular, if the starting ketone is chiral then the epoxide may be generated enantioselectively, which forms the basis of the Shi epoxidation.


Oxone is a non-chlorine shock.
Oxone will break the chlorine-ammonia bond formed when chlorine combines with ammonia, without increasing the chlorine level of the swimming pool.
Shocking is the introduction of a large amount of a chemical that causes contaminants in the pool to be oxidized (burned off).


The most common contaminant is chloramines, which is the combination of chlorine and ammonia.
These compounds are strong eye irritants and produce a strong chlorine odor.
They are eliminated by oxidation.


Oxidation can be accomplished by several means, the most common is the introduction of a chlorine shock, the second is non-chlorine shock.
Non-Chlorine shock provides tremendous versatility for pool and spa owners as well as pool professionals, Oxone is the oxidizer of choice, where the introduction of chlorine, which increases chlorine levels, may be irritating to some bathers.


Oxone is a white, free flowing crystalline granule, is non-toxic, odorless, and easily soluble in water.
Oxone is an efficient, environmentally friendly, and multifunctional acidic oxidant.
Oxone is a free-flowing, white granular solid, soluble in water.


Oxone is present as a component of a triple salt including potassium monopersulfate, potassium bisulfateand potassium sulfate with the formula 2KHSO5·KHSO4·K2SO4.
The oxidation potential of this compound is derived from its peracid chemistry.


Oxone has several important disadvantages and limitations.
While Oxone does oxidize and break down urea and chloramines, nitrate ions are the main oxidation product.
This is an important point to consider because like phosphates, nitrates are great algae food.


Furthermore, Oxone lowers the pH and the total alkalinity.
Oxone shows up as combined chlorine in the DPD test and as free chlorine in the FAS-DPD test.
Oxone oxidizes and reacts with one of the reagents.


This interference can be removed, however, and service technicians should be aware of this point.
Oxone is a strong oxidant with an oxidation potential of similar magnitude to that of chlorine.



USES and APPLICATIONS of OXONE:
Oxone has been used for over 30 years in paper products such as tissue and towel paper, coffee filters and food packaging – products that often come into close contact with humans.
Oxone is used for halogenation of a,b-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.


Oxone is a used for rapid, and good synthesis of oxaziridines.
Oxone is used for halogenation of a,b-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.
Oxone is a reactive oxygen species (ROS) that has an inhibitory effect on the growth of bacteria.


Oxone is used as a disinfectant or sterilant and is often used in wastewater treatment plants to remove organic contaminants such as naphthalene.
The mechanism of action for Oxone involves its reaction with the electron-rich functional groups found on the bacterial cell membrane, which forms peroxides that cause irreversible damage to the cell.


Oxone also reacts with DNA, RNA, and proteins, and is therefore toxic to all cells.
Oxone has been shown to be effective against both Gram-positive and Gram-negative bacteria, but it does not work well against acid-fast bacteria such as Mycobacterium tuberculosis or Mycobacterium avium complex.


Oxone is used for halogenation of a,b-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.
Oxone is used for rapid, and good synthesis of oxaziridines
Oxone may be used as an alternative to transition-metal oxidants for the conversion of aldehydes to carboxylic acids or esters.


Oxone is also used to study fading of an artist′s colorants.
Oxone is a potassium triple salt mainly used as a stable, easy to handle and nontoxic oxidant.
The use of Oxone has increased rapidly due to its inherent stability, the simple handling, the non-toxic nature, the versatility of the reagent and the relatively low cost.


Oxone is used for oral cleaning, swimming pool and hot spring water Disinfection, pulp bleaching.
Oxone provides powerful non-chlorine oxidation for a wide variety of industrial and consumer uses.


Oxone's applications may be found in oral hygiene formulations, pool and spa shock and disinfection, paper recycling, printed circuit board etching, wool shrink proofing, laundry bleaches, precious metal extraction process compounds, such as mercaptans, sulfides, disulfides, and sulfites in waste water treatment.


Oxone's also an oxygen releasing agent in aquiculture and low temperature bleaching agent in detergent formulations.
Disinfectant uses of Oxone : In swimming pools and spas for the purpose of reducing the organic content of the water.
Printed Circuit Board Etching : Oxone is used as a micro-etching for cleaning and preparing copper printed wiring board surfaces.


Paper Recycling : Oxone is a convenient and effective processing aid for re-pulping wet strength resin or secondary fiber furnish.
Textile : Oxone is used as an oxidizer for the treatment of wool to prepare it for the application of shrink-proofing resins and laundry bleach.
Others uses of Oxone : Denture cleansers; Plaster Additive; Auxiliary Agent in organic synthesis; Carpet Browning and water decontamination.


Oxone is a stable, convenient and excellent acidity oxidant being widely used in the following industries; pool and spa, water disinfection, PCB etchant, pulp bleach, wool fabric shrink treatment agents, and metal refining agents.
Oxone is also used in organic synthesis, such as oxidizing the double bonds of organic molecules, or as an initiator in many radical polymerizations.


In addition, Oxone can oxidize the hydrogen sulfide or sulfur containing substances in wastewater, provide oxygen in aquaculture, and bleach to remove stains at a low temperature.
Oxone is used Oxidier Agent, Substitution for Halogen Oxidizer, and Enviromental Friendly.


Oxone is used in AquaculturePotassium Monopersulfate compound is a kind of acid oxidant, a free flowing white granularly powder, and soluble in water.
Oxone is a white, granular, free-fl owing peroxygen that provides powerful non-chlorine oxidation for a wide variety of uses.
Oxone is the active ingredient in most nonchlorine oxidizers used for pool and spa/hot tub oxidation.


Most non-chlorine oxidizers contain 45% of the active ingredient Oxone, but blended compositions are also commercially available that may contain buffers, clarifiers and/or additives for control of algae.
Oxone is not a sanitizer or algaecide and must be used in conjunction with an EPA-registered sanitizer.


The role of Oxone is to provide effective non-chlorine oxidation — in other words, to react with organic contaminants and maintain or restore water clarity.
Always follow label directions when using Oxone products to treat swimming pool and spa/hot tub water.
Oxone is compatible with all sanitizer products and systems.


When used with biguanide systems, follow the biguanide manufacturers’ specific recommendations for the use of pOxone.
It is recommended for use in indoor and outdoor residential and commercial venues.
While there is no specific test to determine when and how much Oxone should be applied, there are guidelines that can be followed to ensure proper use.


The primary parameters to be tested are free and combined chlorine.
Free chlorine should always be tested, and adjusted if necessary, to ensure proper sanitizer levels.
Testing combined chlorine indicates the level of contaminants bound to chlorine and the need for supplemental oxidation.


Pool and hot tub water should be properly balanced.
This requires testing of the pool water balance parameters of pH, carbonate alkalinity, calcium hardness, and stabilizer (i.e., cyanuric acid).
In addition to testing the standard parameters, an overall assessment of pool and hot tub water and air quality should be performed.


Oxone has applications in denture cleansers, swimming pool oxidants, circuit board etchants, pulp recycling, wood cleaning and for other uses in which its combination of powerful oxidation and relative safety are useful.
Oxone is also known as MPS and it is widely used as an oxidizing agent.


Oxone is a stable, convenient, and widely used excellent acidic oxidant.
Oxone's application fields involve oral cleaning, swimming pool and hot spring water disinfection, Circuit board etchant, pulp bleaching, wool fabric anti-shrinkage treatment, precious metal extraction, etc.


Oxone salt is an important auxiliary agent in organic synthesis, which can epoxidize the double bonds in organic molecules.
Oxone is a free radical initiator for many polymerization reactions.
In addition, Oxone can be used as an oxidant for sulfur-containing substances such as hydrogen sulfide in wastewater treatment, a low-temperature oxygen-based bleach in detergent, and an oxygen supply agent in aquaculture.


Oxone can be used in animal breeding industry, cosmetics, daily chemicals, wool spinning and paper industry, water treatment industry, oil field, petrochemical, metal electroplating, smelting, printed circuit board PCB/metal surface treatment, chemical synthesis, etc.
Oxone is used microetching and cleaning of printed wiring/circuit board (PWB)


For PWB industry, microetch solutions used to remove excess graphite and/or carbon black may be based on hydrogen peroxide or sodium persulfate as the oxidizing agent.


For example, a sodium persulfate-based product may be combined with sufficient sulfuric acid to make a microetch bath containing 100 300 grams of sodium persulfate per liter of deionized water and about 1 to 10% by weight sulfuric acid but nowadays, technical people find that Oxone could be used as very good solution as it contains required oxideizer, sulfuric acid as one step solution.


Key Applications of Oxone: Pool & Spa, Pulp & Paper, Electronics, Mining, Water Treatment, HI&I, Denture Cleaning.
Oxone is a white granular product that provides non-chlorinated oxidation in a wide variety of applications.
Oxone's safe to use in a production facility, in the environment, and even as a key ingredient in your denture cleaner!


Most notably, Oxone allows for efficient non-chlorinated oxidation as a pool shock, allowing less use of sanitizer and leaves the pool clean, clear, and swimmable nearly immediately.
The powerful oxidation as a microetchant in printed circuit boards improves process control in multi-step copper etching with a predictable rate to completion.


Oxone is of particular interest in metal plating and mining as it safely, economically, and conveniently oxidizes cyanide in waste streams.
These key benefits of rapid rate of reaction as well as non-chlorinated oxidation has allowed repulping papers with wet strength resins to move their processes to greener methods without sacrificing production time.


Oxone is used to shock pools for a variety of reasons.
Some use Oxone to avoid using chlorine.
When chlorine is used to oxidize pool water, Oxone reacts with bather and other organic wastes, which are primarily nitrogen based compounds, to form chloramines.


These by-products have a foul odor and are considered unpleasant.
Oxone also reacts with the nitrogen- based compounds introduced by bathers, but because it does not contain chlorine, does not form chloramines in its oxidation process.


Also, Oxone dissolves quickly, and does not fade liners.
Oxone works well with chlorine, arguably allowing chlorine to work more efficiently as a sanitizer.
Using Oxone is highly recommended for indoor pools, where there is no sunlight or wind to help break down and carry away combined chlorine.


For all its limitations, Oxone does have its uses.
The most important point to remember is that while it is certainly a strong oxidant, Oxone is NOT a sanitizer, and therefore provides no protection against bacteria and viruses.


Oxone, a stable, convenient and excellent acidity oxidant, is widely used in industries.
Oxone is used in oral hygiene, pool and spa waterdisinfection, PCB etchant, Pulp bleach, wool fabrics shrink treatment agent, precious metal refining agent.
Oxone is also used in organic synthesis, such as epoxidizing the double bonds of organic molecule, or as initiator in many radical polymerization.


In addition, Oxone can oxidize the hydrogen sulfide or sulfur-containing substances in the waster water, provide oxygen in aquaculture, and bleach to remove stains at low temperature.
Oxone is widely used in swimming pools to keep the water clear, thus allowing chlorine in pools to work to sanitize the water rather than clarify the water, resulting in less chlorine needed to keep pools clean.


Oxone is a popular choice is a non-chlorine product with potassium monopersulfate as the active ingredient.
Oxone is a powerful oxidizer with several attractive properties.
Properly applied, Oxone will prevent the formation of new combined chlorine by eliminating organics in the water without creating more combined chlorine.


Bathers can re-enter the water after waiting a short period of time (usually one hour) to allow proper mixing and circulation.
The reaction byproducts are harmless sulfate salts.
For indoor pools, shocking with Oxone is recommended about once a week.


-Water Balance uses of Oxone:
Regardless of the type of shock used, Oxone is important to maintain proper water balance to protect equipment and pool surfaces from corrosion and scaling.
Some shocks containing Oxone are acidic and periodic checking of the alkalinity and pH should be performed.
Oxone, does not contain calcium and hence will not increase calcium levels or cloud the water like some calcium based shocks


-Cleaning uses of Oxone:
Oxone is used widely for cleaning.
Oxone whitens dentures, oxidizes organic contaminants in swimming pools, and cleans chips for the manufacture of microelectronics.


-Organic chemistry uses of Oxone:
Oxone is a versatile oxidant in organic synthesis.
Oxone oxidizes aldehydes to carboxylic acids; in the presence of alcoholic solvents, the esters may be obtained.
Internal alkenes may be cleaved to two carboxylic acids (see below), while terminal alkenes may be epoxidized.

Sulfides give sulfones, tertiary amines give amine oxides, and phosphines give phosphine oxides.
Further illustrative of the oxidative power of this salt is the conversion of an acridine derivative to the corresponding acridine-N-oxide.
Oxone oxidizes sulfides to sulfoxides and then to sulfones.



BENEFITS OF OXONE:
Oxone is a dynamic and potent biosecurity blend, effective against all types of pathogenic viruses, bacteria, fungi, and protozoa.
Oxone can potentially destroy many pathogens of economic importance in aquaculture farming.
Therefore, Oxone can reduce the incidence of disease outbreaks and enhance survivability.
Oxone is biodegradable, eco-friendly & safe for human and animal life.



PHYSICAL AND CHEMICAL PROPERTIES OF OXONE:
Oxone has a very strong and effective non-chlorine oxidation ability, and the use and treatment process meets the requirements of safety and environmental protection.
Therefore, Oxone is widely used in industrial production and consumption.
In general, Oxone is relatively stable, and the decomposition reaction is easy to occur when the temperature is higher than 65.
More active, easy to participate in a variety of chemical reactions, Oxone can be used as oxidants, bleaching agents, catalysts, disinfectants, Etchants, etc.



ADVANTAGES OF OXONE:
One of its greatest advantages is that bathers can reenter the water a short time after Oxone has been added - typically about 30 minutes.
Also, Oxone dissolves quickly, and does not fade liners, arguably allowing to work more efficiently as a sanitizer.
Using Oxone is highly recommended for indoor pools, where there is no sunlight or wind to help break down .
For indoor pools, shocking with Oxone is recommended about once a week.



PRODUCTION OF OXONE:
Oxone is produced from peroxysulfuric acid, which is generated in situ by combining oleum and hydrogen peroxide.
Careful neutralization of this solution with potassium hydroxide allows the crystallization of the triple salt.



SWIMMING POOL SHOCK AND SPA, OXONE:
Oxone can be added to pool water day or night, and swimming caroat, oxone, virkon can resume after a short waiting period to allow for adequate mixing and dispersion throughout the pool.
No mixing is required; Oxone is completely soluble in water and dissolves quickly.

Broadcast monopersulfate shock slowly and uniformly over the surface of the water, adding about two-thirds of the total dose over the deep end.
Shock with the filter running to ensure complete mixing and good circulation.
Oxone is a versatile oxidant.

Oxone oxidizes aldehydes to carboxylic acids; in the presence of alcoholic solvents, the esters may be obtained. Internal alkenes may be cleaved to two carboxylic acids, while terminal alkenes may be epoxidized.
Thioethers give sulfones, tertiary amines give amine oxides, and phosphines give phosphine oxides.

Oxone will also oxidize a thioether to a sulfone with 2 equivalents.
With one equivalent the reaction converting sulfide to sulfoxide is much faster than that of sulfoxide to sulfone, so the reaction can conveniently be stopped at that stage if so desired.



THE ADVANTAGES OF USING OXONE IN SWIMMING POOLS TREATMENT:
*Maximum disinfection efficiency caused by oxidizing properties,
*Restores water cleanliness and transparency,
*Suitable for all types of swimming pools, spas, bathtubs,
*Significantly improves chlorination efficiency through quick oxidization of organic contaminants,
*Very quick action – facility is ready to use after 15 minutes,
*Harmless to swimming pool surfaces, causes no bleaching or discolouration of painted and vinyl-coated surfaces,
*No irritating odour, does not cause allergy as Oxone contains no chloride, aldehydes, alcohol,
*Oxone has no impact on water hardness.



PRODUCTION SITE OF OXONE:
Oxone provides powerful non-chlorine oxidation for a wide variety of industrial and consumer uses.
Oxone’s applications may be found in oral hygiene formulations, pool and spa shock and disinfections, paper recycling, printed circuit board etching, wool shrink proofing, laundry bleaches, precious metal extraction process.
Oxone is an important auxiliary agent in organic synthesis for oxidizing plenty of organics and functioning as the epoxy oxidizer of the twin bonds of organic chemicals.
Oxone’s also a free radicle introductory agent in many polymeric reactions.
Oxone can be used to oxidize hydrogen sulfide (H2S) and other reduced sulfur compounds, such as mercaptans, sulfides, disulfides, and sulfites in waste water treatment.
Oxone’s also an oxygen releasing agent in aquiculture and low temperature bleaching agent in detergent formulations.



THE BEAUTY OF OXONE:
There are some who have turned to Oxone as a means for shocking their pools. KMPS is a non-chlorine oxidizer, whose chemical formula is KHSO5.
Oxone is a strong oxidant with an oxidation potential of similar magnitude to that of chlorine.
While Oxone is a powerful oxidizer, there are several important points to consider about this chemical.



WOOL SHRINKPROOFING OF OXONE:
Oxone is more commonly known name as an oxidizer for wool shrinkproofing treatment.
Oxone is in the form of a granule, easily dissolved, and an aqueous solution contains the dissolved oxidizer is stable for sotrage at a temperature of 32 centigrade. a -S--S-bond is stopped at substantially mono-oxidized state.
Oxone is used odor control agent in wastewater treatment
Oxone is used bleach component in denture cleanser and laundry formulations
Oxone is used activator in antimicrobial compositions
Other uses of Oxone where its combination of powerful oxidation and relative.



PHYSICAL and CHEMICAL PROPERTIES of OXONE:
Molecular weight: 614.7
Appearance: White, free flowing granule
Available Oxygen, % =4.5
KHSO5, %=42.8
Loss on Drying, %=0.15
Bulk Density, g/L=0.80
pH (10g/L,25C): 2.0~2.4
Sieve Residue on 75m test sieve: =90.0
Chemical formula: KHSO5
Molar mass: 152.2 g/mol (614.76 g/mol as triple salt)
Appearance: Off-white powder
Solubility in water: Decomposes
Physical state: granular

Color: white
Odor: none
Melting point/freezing point:
Melting point/range: Decomposes before melting.
Initial boiling point and boiling range: Not applicable
Flammability (solid, gas): The product itself does not burn,
but it is slightly oxidizing
(active oxygen content ca. 2%).
Upper/lower flammability or explosive limits: No data available
Flash point: does not flashNot applicable
Autoignition temperature: Not applicable
Decomposition temperature: No data available
pH: 2,1 at 30 g/l at 77 °C

Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility 357 g/l at 22 °C - soluble
Partition coefficient: n-octanol/water: No data available
Vapor pressure: < 0,0000017 hPa
Density: 1,100 - 1,400 g/cm3
Relative density: 2,35 at 20 °C
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: Not classified as explosive.
Oxidizing properties: The substance or mixture is not classified as oxidizing.

Other safety information:
Bulk density 1.100 - 1.400 kg/m3
APPEARANCE: WHITE POWDER OR GRANULE
ACTIVE OXYGEN%: ≧4.50
ACTIVE COMPONENT(KHSO5)%: ≧42.80
WATER SOLUBILITY(G/L20C): 256
MOISTURE%: ≤0.1
BULKDENSITYG/CM*3: 1.00-1.30
PHTEST(10G/L,25C): 2.0-2.3
PARTICALSIZE(20-200MESH): ≧90.0
CAS: 70693-62-8
EINECS: 274-778-7

InChI: InChI=1/K.H2O6S/c;1-5-6-7(2,3)4/h;1H,(H,2,3,4)/q+1;/p-1/rHKO6S/c1-5-6-7-8(2,3)4/h(H,2,3,4)
InChIKey: HVAHYVDBVDILBL-UHFFFAOYSA-M
Molecular Formula: HKO6S
Molar Mass: 168.17
Density: 1.15
Melting Point: 93℃
Water Solubility: Soluble in water (100 mg/ml).
Solubility: 250-300g/l soluble
Appearance: White crystalline powder
Specific Gravity: 1.12-1.20
Color: white
Exposure Limit ACGIH: TWA 0.1 mg/m3
PH: 2-3 (10g/l, H2O, 20℃)

Storage Condition: Store at <= 20°C.
Stability: Stable.
Sensitive: Hygroscopic
MDL: MFCD00040551
Appearance: free-flowing granule
KHSO5, %: ≥42.8
Active Component (KHSO5.KHSO4.K2SO4), %: ≥99
Moisture, %: ≤0.5
Bulk Density, g/L: 800-1200
pH(1%suspension): 2.0~2.3
Particle Size Distribution(0.850~0.075mm),%: ≥90.0
Stability ,active oxygen loss/month, %: ≤1.0
Solubility(20ºC,100g water),g: ≥14.5
CAS: 70693-62-8
EINECS: 274-778-7
InChI: InChI=1/K.H2O6S/c;1-5-6-7(2,3)4/h;1H,(H,2,3,4)/q+1;/p-1/rHKO6S/c1-5-6-7-8(2,3)4/h(H,2,3,4)
InChIKey: HVAHYVDBVDILBL-UHFFFAOYSA-M

Molecular Formula: HKO6S
Molar Mass: 168.17
Density: 1.15
Melting Point: 93℃
Water Solubility: Soluble in water (100 mg/ml).
Solubility: 250-300g/l soluble
Appearance: White crystalline powder
Specific Gravity: 1.12-1.20
Color: white
Exposure Limit ACGIH: TWA 0.1 mg/m3
PH: 2-3 (10g/l, H2O, 20℃)
Storage Condition: Store at <= 20°C.
Stability: Stable.
Sensitive: Hygroscopic
MDL: MFCD00040551



FIRST AID MEASURES of OXONE:
-Description of first-aid measures:
*General advice:
First aiders need to protect themselves.
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
Call in physician.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Call a physician immediately.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Immediately call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Make victim drink water (two glasses at most).
Call a physician immediately.
Do not attempt to neutralise.
-Indication of any immediate medical attention and special treatment needed
No data available



ACCIDENTAL RELEASE MEASURES of OXONE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of OXONE:
-Extinguishing media:
*Suitable extinguishing media:
Use extinguishing measures that are appropriate to local circumstances and the surrounding environment.
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Suppress (knock down) gases/vapors/mists with a water spray jet.
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of OXONE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
Acid-resistant protective clothing
*Respiratory protection:
Recommended Filter type: Filter type P2
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of OXONE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
hygroscopic
*Storage class:
Storage class (TRGS 510): 8B:
Non-combustible



STABILITY and REACTIVITY of OXONE:
-Reactivity:
No data available
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available




OXONE (POTASSIUM MONOPERSULFATE)
Oxone (potassium monopersulfate), a white, free flowing crystalline granule, is non-toxic, odorless, and easily soluble in water.
Oxone (potassium monopersulfate) is used in various chemical reactions where a strong oxidizing agent is required.
Oxone (potassium monopersulfate) can be employed in the synthesis of certain organic compounds.

CAS Number: 70693-62-8
Molecular Formula: HKO6S
Molecular Weight: 168.17
EINECS Number: 274-778-7

Synonyms: OXONE(R), monopersulfate compound, pentapotassium;hydrogen sulfate;oxido hydrogen sulfate;sulfate, Potassium peroxymonosulfate sulfate (K5(HSO3(O2))2(HSO4)(SO4)), Potassium peroxymonosulfate sulfate (K5[HSO3(O2)]2(HSO4)(SO4)), MFCD00040551, Oxone, monopersulfate, CARO'S TRIPLE SALT, DTXSID8051415, POTASSIUM CAROATE [INCI], HJKYXKSLRZKNSI-UHFFFAOYSA-I, AKOS015912003, AKOS030228420, POTASSIUM MONOPERSULFATE [INCI], POTASSIUM PERSULFATE TRIPLE SALT, FT-0697154, O0310, D78337, Potassium monopersulfate triple salt, >=47% KHSO5 basis, POTASSIUM PEROXYMONOSULFATE SULFATE (2KHSO5.KHSO4.K2SO4)

Oxone (potassium monopersulfate) is known for its ability to convert hypochlorite ion into free chlorine.
Oxone (potassium monopersulfate) also produces free chlorine without oxidizing ammonia.
Oxone (potassium monopersulfate) can be used to control pH fluctuations in water treatment systems.

Oxone (potassium monopersulfate) for swimming pools.
Oxone (potassium monopersulfate) is frequently used by swimming pool owners to make chlorination water.
Oxone (potassium monopersulfate) is also used to treat industrial wastewater.

In swimming pools, Oxone (potassium monopersulfate) is an effective oxidizer for controlling algae.
Oxone (potassium monopersulfate) also helps prevent the formation of precipitates that can cloud the water.
The benefits of Oxone (potassium monopersulfate) include reducing phosphates and chemical use, stabilizing pH in a pool, eliminating algae.

Oxone (potassium monopersulfate) also increases circulation, which saves energy.
As a result, pools using Oxone have increased clarity, and decreases the likelihood of chemical and odor problems.
Oxone (potassium monopersulfate) is not the same as the Chlorine you are used to using.

Discretely, Oxone (potassium monopersulfate) is similar to bleach, but it is not a typical bleach product.
To determine advantages in your pool, must first understand the chemical formula.
Because Oxone (potassium monopersulfate) is a salt, it has a chemical formula containing Potassium.

Other ingredients, such as Oxygen, and Sulfur (Sulfur is the "E" in Oxone) are added.
Using this formula, the official chemical name for Oxone (potassium monopersulfate), and if was not derived from bleach, it would be considered a bleach product.
Oxone (potassium monopersulfate) is also called MPS, or Potassium Monopersulfate.

Oxone (potassium monopersulfate) does not contain chlorine, as it is a potassium salt of peroxymonosulfuric acid.
Oxone (potassium monopersulfate) is marketed as a popular non-chlorine based shock.
Oxone (potassium monopersulfate) is primary swimming pool use is to oxidize any contaminants in the water, leaving chlorine or bromine sanitizers already present in the water to focus on sanitizing the water.

There are several advantages of using Oxone (potassium monopersulfate) in swimming pools: Since there is no chlorine added, the swimming pool is available for swimming immediately after the shock has dissolved and time has been given for the oxidation process to complete.
Oxidation is usually complete in about one to two hours, versus eight or more hours for chlorine-based shock.
Oxone (potassium monopersulfate) use can decrease, as less chlorine is needed to oxidize organic and inorganic matter in the pool.

There are several disadvantage of using Oxone (potassium monopersulfate) as a shock treatment in swimming pools.
Chlorine tests can read incorrectly high in DPD or FAS-DPD tests, as the non-chlorine shock may show up as combined chlorine in these tests.
If adequate chlorine sanitizer levels are not maintained, then adding non-chlorine shock like MSP may increase the risk of algae growth due to possible nitrate creation from adding Oxone (potassium monopersulfate).

Oxone (potassium monopersulfate) is the potassium salt of peroxymonosulfuric acid, which is widely used as an oxidizing agent.
Oxone (potassium monopersulfate), contain potassium monopersulfate for their main ingredient, as a non-chlorine shock agent; Oxone (potassium monopersulfate) breaks the chlorine–ammonia bond formed when chlorine combines with ammonia, without increasing the chlorine level of the swimming pool; hence, Oxone (potassium monopersulfate) can be used in swimming pools to keep the water clear.
Oxone (potassium monopersulfate) is a powerful oxidizer with several attractive properties.

Properly applied, Oxone (potassium monopersulfate) will prevent the formation of new combined chlorine by eliminating organics in the water without creating more combined chlorine.
Bathers can re-enter the water after waiting a short period of time (usually one hour) to allow proper mixing and circulation.
The reaction byproducts are harmless sulfate salts.

Oxone (potassium monopersulfate) can be prepared by reacting a concentrated solution of Caro's acid with a potassium salt, such as potassium carbonate.
Oxone (potassium monopersulfate) can also be used.
Oxone (potassium monopersulfate) is sold under the name of Oxone in most swimming pool stores and various home-improvement and gardening retailer stores.

Oxone (potassium monopersulfate) is a kind of acid oxidant, a free flowing white granularly powder, and soluble in water.
Other Names are Oxone (potassium monopersulfate), potassium monopersulfate compound, Potassium hydrogen sulfate, PMPS,KMPS, ect.
Oxone (potassium monopersulfate) is a free-flowing, white granule which is soluble in water (20°C, 256 g/L).

The composition of Oxone (potassium monopersulfate) includes Potassium Hydrogen Peroxymonosulfate (KHSO5), (KHSO4) and Potassium Sulfate(K2SO4).
Oxone (potassium monopersulfate) is exceedingly hygroscopic and is readily soluble in water to form the monopersulfate salts.
Oxone (potassium monopersulfate) has very low solubility in organic solvents, but excellent solubility in acids and aqueous solutions of acids and bases.

Oxone (potassium monopersulfate), monopersulfate compound is a potassium triple salt mainly used as a stable, easy to handle and nontoxic oxidant.
Oxone (potassium monopersulfate) is the potassium salt of peroxymonosulfuric acid.
Usually Oxone (potassium monopersulfate) refers to the triple salt known as oxone.

The standard electrode potential for Oxone (potassium monopersulfate) is +1.81 V with a half reaction generating the hydrogen sulfate (pH = 0):
HSO5− + 2 H+ + 2 e− → HSO4− + H2O
Oxone (potassium monopersulfate) is used for halogenation of a,b-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.

Oxone (potassium monopersulfate) can be found in certain household cleaning products.
Oxone (potassium monopersulfate) is widely used as an oxidizing agent, for example, in pools and spas (usually referred to as monopersulfate or "MPS").
Oxone (potassium monopersulfate) can also be obtained via electrolysis of potassium persulfate in sulfuric acid. Potassium sulfate appears as a byproduct.

Adding hydrogen peroxide to Oxone (potassium monopersulfate) also yields potassium peroxymonosulfate.
Oxone (potassium monopersulfate) also reacts with DNA, RNA, and proteins, and is therefore toxic to all cells.
Oxone (potassium monopersulfate) has been shown to be effective against both Gram-positive and Gram-negative bacteria, but it does not work well against acid-fast bacteria such as Mycobacterium tuberculosis or Mycobacterium avium complex.

Oxone (potassium monopersulfate) is a free-flowing, white granular solid, soluble in water.
Oxone (potassium monopersulfate) is present as a component of a triple salt including potassium monopersulfate, potassium bisulfateand potassium sulfate with the formula 2KHSO5·KHSO4·K2SO4.

The oxidation potential of Oxone (potassium monopersulfate) is derived from its peracid chemistry.
Oxone (potassium monopersulfate) provides powerful non-chlorine oxidation for a wide variety of industrial and consumer uses.
Oxone (potassium monopersulfate)’s applications may be found in oral hygiene formulations, pool and spa shock and disinfections, paper recycling, printed circuit board etching, wool shrink proofing, laundry bleaches, precious metal extraction process.

Oxone (potassium monopersulfate) is an important auxiliary agent in organic synthesis for oxidizing plenty of organics and functioning as the epoxy oxidizer of the twin bonds of organic chemicals.
Oxone (potassium monopersulfate)’s also a free radicle introductory agent in many polymeric reactions.
Oxone (potassium monopersulfate) can be used to oxidize hydrogen sulfide (H2S) and other reduced sulfur compounds, such as mercaptans, sulfides, disulfides, and sulfites in waste water treatment.

Oxone (potassium monopersulfate)’s also an oxygen releasing agent in aquiculture and low temperature bleaching agent in detergent formulations.
Oxone (potassium monopersulfate) can be added to pool water day or night, and swimming caroat, oxone, virkon can resume after a short waiting period to allow for adequate mixing and dispersion throughout the pool.
No mixing is required; Oxone (potassium monopersulfate) is completely soluble in water and dissolves quickly.

Broadcast monopersulfate shock slowly and uniformly over the surface of the water, adding about two-thirds of the total dose over the deep end.
Shock with the filter running to ensure complete mixing and good circulation.
Oxone (potassium monopersulfate) is a versatile oxidant.

Oxone (potassium monopersulfate) oxidizes aldehydes to carboxylic acids; in the presence of alcoholic solvents, the esters may be obtained.
Internal alkenes may be cleaved to two carboxylic acids, while terminal alkenes may be epoxidized.
Thioethers give sulfones, tertiary amines give amine oxides, and phosphines give phosphine oxides.

Oxone (potassium monopersulfate) will also oxidize a thioether to a sulfone with 2 equivalents.
With one equivalent the reaction converting sulfide to sulfoxide is much faster than that of sulfoxide to sulfone, so the reaction can conveniently be stopped at that stage if so desired.
Oxone (potassium monopersulfate) is a chlorine free and versatile oxidant, provides powerful non-chlorine oxidation and microbiological effectiveness for a wide variety of industrial and consumer use.

The chemical formula for Oxone (potassium monopersulfate) is often written as 2KHSO5·KHSO4·K2SO4.
Oxone (potassium monopersulfate) is a triple salt, which means it contains three different salts: potassium hydrogen peroxymonosulfate (2KHSO5), potassium bisulfate (KHSO4), and potassium sulfate (K2SO4).
Oxone (potassium monopersulfate) is a powerful oxidizing agent.

Oxone (potassium monopersulfate) releases active oxygen upon dissolution in water, which makes it effective in breaking down organic and inorganic contaminants.
This property is particularly valuable in applications such as water treatment and cleaning.
Oxone (potassium monopersulfate) is commonly used in the disinfection of spas and hot tubs.

Oxone (potassium monopersulfate) helps control the growth of bacteria and other microorganisms in the warm water environments of these recreational facilities.
Oxone (potassium monopersulfate) can be used in conjunction with bromine as a disinfectant in hot tubs and spas.
This combination is often preferred over using chlorine in these settings.

Due to its bleaching properties, Oxone (potassium monopersulfate) is utilized in the hair dyeing industry to decolorize hair.
Oxone (potassium monopersulfate) is also employed in the textile industry for bleaching fabrics.
In certain organic reactions, Oxone (potassium monopersulfate) can serve as a catalyst for oxidation processes.

Oxone (potassium monopersulfate) is use in these reactions is dependent on the specific requirements of the synthesis.
Oxone (potassium monopersulfate) can act as a polymerization initiator in certain polymerization reactions.
Oxone (potassium monopersulfate) contributes to the initiation of the polymerization process, leading to the formation of polymers.

Oxone (potassium monopersulfate) has relatively high oxidation reduction potential.
Therefore, Oxone (potassium monopersulfate) is a highly effective oxidant and disinfectant.
Oxone (potassium monopersulfate) is a kind of inorganic acid oxidant, and potassium potassium persulfate compound and potassium monopersulfate trivalent salt peroxide single sulfate, Oxone, potassium monopersulfate compound, potassium monopersulfate triple salt or potassium peroxymonopersulfate.

Nevertheless, Oxone (potassium monopersulfate) is the basic active component of the functional chemical Oxone, Caroat, ZA200/100 and Basolan2448.
Oxone (potassium monopersulfate) per se is a relatively obscure salt, but its derivative called oxone is of commercial value.
Oxone (potassium monopersulfate) refers to the triple salt 2KHSO5·KHSO4·K2SO4.

Oxone (potassium monopersulfate) has a longer shelflife than does potassium peroxymonosulfate.
Oxone (potassium monopersulfate) a white, water-soluble solid, oxone loses <1% of its oxidizing power per month.
Oxone (potassium monopersulfate) is produced from peroxysulfuric acid, which is generated in situ by combining oleum and hydrogen peroxide.

Careful neutralization of this solution with potassium hydroxide allows the crystallization of the triple salt.
Oxone (potassium monopersulfate) is a free-flowing powder chemical microetchant for electronics and printed wiring board manufacturing industries.
Other benefits include: free-flowing powder, high etch rates that are uniform and predictable, excellent bonding morphology, well-defined surface topography, contaminant removal, high rinsability, long bath life with simple analysis and control, better performance at lower temperatures, and allowing for energy and cost savings.

Oxone (potassium monopersulfate) is a versatile oxidant in organic synthesis.
Oxone (potassium monopersulfate) oxidizes aldehydes to carboxylic acids; in the presence of alcoholic solvents, the esters may be obtained.
Internal alkenes may be cleaved to two carboxylic acids, while terminal alkenes may be epoxidized.

Sulfides give sulfones, tertiary amines give amine oxides, and phosphines give phosphine oxides.
Further illustrative of the oxidative power of this salt is the conversion of an acridine derivative to the corresponding acridine-N-oxide.
Oxone (potassium monopersulfate) is widely used as an oxidizing agent.

Oxone (potassium monopersulfate) is the potassium salt of peroxymonosulfuric acid.
The triple salt 2KHSO5·KHSO4·K2SO4 (known by the trade name Oxone) is a form with higher stability.
The standard electrode potential for this compound is 1.81 V with a half-reaction generating the hydrogen sulfate Oxone (potassium monopersulfate) is also used as a wet strength resin paper repulping aid, metal surface treatment agent, selective oxidizer in chemical synthesis, wool shrink proofing treatment, wastewater treatment and odor control agent.

Oxone (potassium monopersulfate) is an inorganic chemical compound.
Oxone (potassium monopersulfate) is primarily used for the treatment of wastewater.
Oxone (potassium monopersulfate) occurs as white crystals or powder with hygroscopic properties.

Oxone (potassium monopersulfate) is a used for rapid, and good synthesis of oxaziridines.
Oxone (potassium monopersulfate), often marketed under the trade name "Oxone," is a chemical compound with the formula 2KHSO5·KHSO4·K2SO4.
Oxone (potassium monopersulfate) is a triple salt that contains potassium hydrogen peroxymonosulfate, and it is commonly used as an oxidizing agent in various applications.

Oxone (potassium monopersulfate) is employed as a non-chlorine shock treatment for pool and spa water.
Oxone (potassium monopersulfate) helps eliminate organic contaminants and enhances water clarity without the strong odor associated with chlorine-based treatments.
Oxone (potassium monopersulfate) is an efficient, environmentally friendly, and multifunctional acidic oxidant.

Oxone (potassium monopersulfate) is a strong oxidizer, capable of oxidizing organic substances into various compounds, such as: aldehydes to carboxylic acids, alcoholic solvents to their coresponding esters, cleaving internal alkenes to two carboxylic acids and terminal alkenes to epoxides, ketones to dioxiranes, thioethers to sulfones, tertiary amines to amine oxides and phosphines to phosphine oxides.
Another method involves the hydrolysis of Oxone (potassium monopersulfate) at 100 °C to yield peroxydisulfuric acid.
Oxone (potassium monopersulfate) is added, and the solution is filtered to remove the resulting potassium sulfate.

The filtrate is freeze-dried and then washed with distilled water and filtered again at room temperature.
The resulting filtrate is chilled on an ice bath, and the product is recrystallized for better purity.
Oxone (potassium monopersulfate) is a reactive oxygen species (ROS) that has an inhibitory effect on the growth of bacteria.

Oxone (potassium monopersulfate) is used as a disinfectant or sterilant and is often used in wastewater treatment plants to remove organic contaminants such as naphthalene.
The mechanism of action for Oxone involves its reaction with the electron-rich functional groups found on the bacterial cell membrane, which forms peroxides that cause irreversible damage to the cell.

Density: 1.15
storage temp.: Store at <= 20°C.
solubility: 250-300g/l soluble
form: solid
Specific Gravity: 1.12-1.20
color: white
PH: 2-3 (10g/l, H2O, 20℃)
Water Solubility: Soluble in water (100 mg/ml).
Sensitive: Hygroscopic
Exposure limits ACGIH: TWA 0.1 mg/m3
Stability: Stable. Oxidizer. Incompatible with combustible materials, bases.
InChIKey: HVAHYVDBVDILBL-UHFFFAOYSA-M
LogP: -3.9 at 25℃

Oxone (potassium monopersulfate) is a very stable peroxygen in the solid state and loses less than 0.5% (relative) of its activity per month when stored under recommended conditions.
However, like all other peroxygens, Oxone (potassium monopersulfate) undergoes very slow disproportionation with the liberation of heat and oxygen gas.
The stability is reduced by the presence of small amounts of moisture, alkaline chemicals, chemicals that contain water of hydration, transition metals in any form, and/or any material with which Oxone can react.

Since the decomposition of Oxone (potassium monopersulfate) is exothermic, the decomposition can self-accelerate if storage conditions allow the product temperature to rise.
The stability is adversely affected by higher pH, especially above pH 7. A point of minimum stability exists at about pH 9, at which the concentration of the mono-anion HSO5 - is equal to that of the.
Cobalt, nickel, and manganese are particularly strong catalysts for the decomposition of Oxone (potassium monopersulfate) in solution; the degree to which catalysis occurs is dependent on the concentrations of Oxone and of the metal ion.

Oxone (potassium monopersulfate) is more commonly known name as an oxidizer for wool shrinkproofing treatment.
Oxone (potassium monopersulfate) is in the form of a granule, easily dissolved, and an aqueous solution contains the dissolved oxidizer is stable for storage at a temperature of 32 centigrade.
Oxone (potassium monopersulfate) can be added to pool water day or night, and swimming caroat, oxone, virkon can resume after a short waiting period to allow for adequate mixing and dispersion throughout the pool.

Oxone (potassium monopersulfate) is completely soluble in water and dissolves quickly.
Broadcast monopersulfate shock slowly and uniformly over the surface of the water, adding about two-thirds of the total dose over the deep end.
Shock with the filter running to ensure complete mixing and good circulation.

Oxone (potassium monopersulfate) is a versatile oxidant.
Oxone (potassium monopersulfate) oxidizes aldehydes to carboxylic acids; in the presence of alcoholic solvents, the esters may be obtained.
Internal alkenes may be cleaved to two carboxylic acids, while terminal alkenes may be epoxidized.

Thioethers give sulfones, tertiary amines give amine oxides, and phosphines give phosphine oxides.
Oxone (potassium monopersulfate) will also oxidize a thioether to a sulfone with 2 equivalents.
With one equivalent the reaction converting sulfide to sulfoxide is much faster than that of sulfoxide to sulfone, so the reaction can conveniently be stopped at that stage if so desired.

Oxone (potassium monopersulfate) converts ketones to dioxiranes.
The synthesis of dimethyldioxirane (DMDO) from acetone is representative.
Dioxiranes are versatile oxidising agents and may be used for the epoxidation of olefins.

In particular, if the starting ketone is chiral then the epoxide may be generated enantioselectively, which forms the basis of the Shi epoxidation.
Oxone (potassium monopersulfate) is a white granular product that provides non-chlorinated oxidation in a wide variety of applications.
Oxone (potassium monopersulfate)'s safe to use in a production facility, in the environment, and even as a key ingredient in your denture cleaner.

Most notably, the active ingredient allows for efficient non-chlorinated oxidation as a pool shock, allowing less use of sanitizer and leaves the pool clean, clear, and swimmable nearly immediately.
The powerful oxidation as a microetchant in printed circuit boards improves process control in multi-step copper etching with a predictable rate to completion.
Oxone (potassium monopersulfate) is of particular interest in metal plating and mining as it safely, economically, and conveniently oxidizes cyanide in waste streams.

These key benefits of rapid rate of reaction as well as non-chlorinated oxidation has allowed repulping papers with wet strength resins to move their processes to greener methods without sacrificing production time.
Oxone (potassium monopersulfate)'s aqueous solution oxidation state is pink, the reduced state is colorless, easy for users to judge the effectiveness of a disinfectant, avoid ineffective disinfection.
Multi-function, multi-purpose: Applicable to a variety of places disinfection: can be used for farm office, pet operating room, clinic room, canteen, dormitory and other disinfection.

Suitable for disinfection of various methods: can be used for environment, clothing, rubber boots, water supply system, equipment, apparatus, washbasin disinfection.
One operation, multiple harvests: in the disinfection process, Oxone (potassium monopersulfate) can effectively reduce the odor and improve the air quality while suppressing and killing the pathogenic microorganisms.
Oxone (potassium monopersulfate) is a non-chlorine oxidizer and is used as an oxidizing agent in the pool and spa industry.
The active ingredients of Oxone are potassium sulfate, potassium monopersulfate, and potassium bisulfide.

Oxone (potassium monopersulfate) is popularly known by its trade names such as Oxone, Caroat, and non-chlorine shock.
Oxone (potassium monopersulfate) has a similar magnitude of oxidation potential as chlorine and does not form chloramines during its oxidation process.
In addition, Oxone (potassium monopersulfate) is highly soluble in water and provides high microbiological effectiveness and powerful non-chlorine oxidation for various industrial applications.

Oxone (potassium monopersulfate) is widely used as a disinfectant in wastewater treatment, swimming pools, etc., for reducing the organic and microbe content of the water.
Oxone (potassium monopersulfate) is used as a cleaning agent in printed circuit boards, as an oxidizer agent for treating wool, and as an auxiliary agent for organic chemicals.
In addition, Oxone (potassium monopersulfate) finds application in paper recycling, carpet browning, and oral hygiene formulations.

Oxone (potassium monopersulfate) offers low shrink resistance during the wool as well as laundry bleaching processes.
Oxone (potassium monopersulfate) aids in the quick cleaning of pools and leads to less usage of sanitizer due to its strong non-chlorinated oxidation potential.
Oxone (potassium monopersulfate) is the first raw material verified by Green Seal for removal of wet strength resins in paper repulping.

The peroxymonosulfate ion (HSO5-) is a key component that contributes to its strong oxidizing capabilities.
This active oxygen can break down organic compounds and microorganisms, making Oxone effective in various applications.
Historically, repulping aids have been chlorine-based.

However, chlorine-based products can negatively impact repulping operations, degrade fiber quality, and pose environmental concerns from toxic organochlorine (AOX) generation.
Oxone (potassium monopersulfate) is chlorine-free, meaning chlorine can be eliminated from the repulping process.
Consequently, chlorinated by-products in the process wastewater can be significantly reduced or eliminated.

For PWB industry, Oxone (potassium monopersulfate)s used to remove excess graphite and/or carbon black may be based on hydrogen peroxide or sodium persulfate as the oxidizing agent.
For example, a Oxone (potassium monopersulfate) may be combined with sufficient sulfuric acid to make a microetch bath containing 100 300 grams of sodium persulfate per liter of deionized water and about 1 to 10% by weight sulfuric acid.

Oxone (potassium monopersulfate) is more commonly known name as an oxidizer for wool shrinkproofing treatment.
Oxone (potassium monopersulfate) is in the form of a granule, easily dissolved, and an aqueous solution contains the dissolved oxidizer is stable for sotrage at a temperature of 32 centigrade.
Oxone (potassium monopersulfate) is widely used as an oxidizing agent, for example, in pools and spas (usually referred to as monopersulfate or “MPS”).

Oxone (potassium monopersulfate) is the potassium salt of peroxymonosulfuric acid.
Usually Oxone (potassium monopersulfate) refers to the triple salt known as oxone.
Oxone (potassium monopersulfate) per se is a relatively obscure salt, but its derivative called oxone is of commercial value.

Oxone (potassium monopersulfate) refers to the triple salt 2KHSO5·KHSO4·K2SO4.
Oxone (potassium monopersulfate) has a longer shelflife than does potassium peroxymonosulfate.
Oxone (potassium monopersulfate) a white, water-soluble solid, oxone loses <1% of its oxidizing power per month.

Oxone (potassium monopersulfate) is used widely for cleaning.
Oxone (potassium monopersulfate) whitens dentures, oxidizes organic contaminants in swimming pools, and cleans chips for the manufacture of microelectronics.
Oxone (potassium monopersulfate) is a versatile oxidant in organic synthesis.

Oxone (potassium monopersulfate) oxidizes aldehydes to carboxylic acids; in the presence of alcoholic solvents, the esters may be obtained.
Internal alkenes may be cleaved to two carboxylic acids, while terminal alkenes may be epoxidized.
Sulfides give sulfones, tertiary amines give amine oxides, and phosphines give phosphine oxides.

Oxone (potassium monopersulfate) oxidizes sulfides to sulfoxides and then to sulfones.
Oxone (potassium monopersulfate) also converts ketones to dioxiranes.
Oxone (potassium monopersulfate) is applied in wastewater treatment to break down and remove pollutants.

Oxone (potassium monopersulfate) is strong oxidizing capabilities aid in the degradation of organic compounds in wastewater.
Oxone (potassium monopersulfate) is generally considered safer than some alternative oxidizing agents, users should still adhere to safety guidelines.
This includes proper storage, handling, and protection measures such as wearing appropriate personal protective equipment (PPE).

Oxone (potassium monopersulfate) can cause irritation to the skin, eyes, and respiratory system.
Oxone (potassium monopersulfate)'s important to seek medical attention if exposure occurs and to follow first aid measures as specified in the product's safety data sheet.
Oxone (potassium monopersulfate)need to comply with relevant regulations and guidelines concerning its production, transportation, and use.

If a decomposition is associated with high temperature, decomposition of the constituent salts of Oxone may generate sulfuric acid, sulfur dioxide, or sulfur trioxide.
Oxone (potassium monopersulfate) operates as an oxidizing agent through the release of active oxygen species.
The decomposition products, Oxone (potassium monopersulfate) and hydrogen peroxide, are generally less harmful to the environment.

Beyond its applications in water treatment, Oxone (potassium monopersulfate) is used in chemical synthesis and organic chemistry.
Oxone (potassium monopersulfate) is strong oxidizing properties make it valuable in various laboratory and industrial processes for the oxidation of organic compounds.
Oxone (potassium monopersulfate) is a stable compound when stored properly. It should be kept in a cool, dry place, away from incompatible substances.

Checking the expiration date and following storage recommendations are important for maintaining its effectiveness.
Oxone (potassium monopersulfate) is often available in granular or powdered form and is typically packaged in containers designed to protect it from moisture and contamination.
Oxone (potassium monopersulfate) is the basic raw material for the preparation of Dioxirasnes (Dioxirasnes) series catalysts, such as DMD and TFD.

With its mild reaction conditions, highly effective oxidation activity and excellent selectivity, the Dioxirasnes has opened up a new path for the asymmetric reaction and the synthesis of natural drugs.
In the design of olefin asymmetric reaction catalyst, chiral amine, chiral imide salt polymerization initiator, polymerization of vinyl acetate, ethyl acrylate and acrylonitrile can be oxidized in situ. Polymerization of vinyl monomers; Adhesive, blending agent.
Oxone (potassium monopersulfate) is used in water treatment processes, particularly in swimming pools and spas.

Oxone (potassium monopersulfate) helps to oxidize and eliminate organic contaminants, bacteria, and algae. Unlike chlorine-based treatments, Oxone (potassium monopersulfate) does not produce chloramines, reducing the characteristic chlorine smell and irritation associated with traditional pool treatments.
In swimming pool maintenance, Oxone (potassium monopersulfate) is often employed as a shock treatment.
Shocking a pool involves adding a large dose of oxidizer to rapidly eliminate contaminants and restore water clarity.

Oxone (potassium monopersulfate) is generally compatible with a wide range of pool and spa chemicals.
However, Oxone (potassium monopersulfate)'s important to follow manufacturer recommendations and guidelines to ensure proper usage and avoid potential chemical reactions that could compromise water quality.
Oxone (potassium monopersulfate) is considered a more environmentally friendly oxidizing agent compared to some alternatives.

Uses:
Oxone (potassium monopersulfate) works very well in effluent treatment: Oxidative treatment of problematic effluents; sulfide oxidation, nitrite oxidation, and cyanide detoxification.
Applied in mold remediation processes for breaking down mold and mildew in buildings.
Oxone (potassium monopersulfate) is used in veterinary practices for disinfecting equipment and ensuring a clean environment.

Oxone (potassium monopersulfate) has been used in photography for its bleaching properties in certain photographic processes.
Included in some household disinfectants and cleaning products for its ability to eliminate bacteria and viruses.
In agriculture, Oxone (potassium monopersulfate) may be used for certain soil and water treatments.

Oxone (potassium monopersulfate) can be used in the dairy industry for cleaning and sanitizing equipment involved in milk processing.
Oxone (potassium monopersulfate) can be employed for dechlorination purposes, helping to remove or neutralize chlorine in water.
Oxone (potassium monopersulfate) is used in the treatment of water in cooling towers to control microbial growth and prevent scaling and corrosion.

In the cosmetics industry, Oxone (potassium monopersulfate) may be used in certain formulations for its oxidizing and bleaching properties.
Apart from bleaching, Oxone (potassium monopersulfate) can find applications in the pulp and paper industry for certain oxidation reactions.
Oxone (potassium monopersulfate) is used in various hygiene and sanitation applications, including in the formulation of hand sanitizers and surface disinfectants.

Oxone (potassium monopersulfate) employed in air and water purification systems to eliminate odors and contaminants.
Oxone (potassium monopersulfate) may be used in electroplating processes for specific oxidation reactions.
Oxone (potassium monopersulfate) is used in the treatment of medical waste to ensure proper disinfection before disposal.

Oxone (potassium monopersulfate) can be used for soil sterilization and to control certain pests and diseases.
The addition of Oxone leads to the generation of oxygen and improved product characteristics (e.g. thermal insulation, water absorbency, mechanical properties).
Oxone (potassium monopersulfate) is utilized in the microelectronics and semiconductor industry for the cleaning and etching of silicon wafers and other electronic components.

Oxone (potassium monopersulfate) can be used for cleaning and disinfecting dental equipment and molds.
Oxone (potassium monopersulfate) is employed in aquaculture for water treatment to control and eliminate harmful microorganisms, ensuring a healthier environment for aquatic life.
In certain applications within the oil and gas industry, Oxone (potassium monopersulfate) may be used for its oxidizing properties in the treatment of water or other substances.

Oxone (potassium monopersulfate) is used in environmental testing laboratories for specific oxidation reactions and analyses.
In some cases, Oxone (potassium monopersulfate) is used in the food and beverage industry for cleaning and disinfecting equipment.
Oxone (potassium monopersulfate) may be employed for sterilization purposes in certain medical and laboratory settings.

Oxone (potassium monopersulfate) is employed as a bleaching agent in the textile and paper industries.
Oxone (potassium monopersulfate) may find applications in the leather industry for certain oxidation and bleaching processes.
Applied as a fungicide in certain agricultural settings to control fungal infections in crops.

Oxone (potassium monopersulfate) is used in soil remediation projects to break down and neutralize contaminants.
Oxone (potassium monopersulfate) can be employed for odor control in various industrial and environmental settings.
Oxone (potassium monopersulfate) can be used in the treatment of metal surfaces to remove oxides and scale, preparing them for subsequent processes such as coating or plating.

In the electronics industry, Oxone (potassium monopersulfate) might find applications in the cleaning and preparation of electronic components and circuit boards.
Oxone (potassium monopersulfate) can be utilized in aquaculture for the disinfection of water and equipment to maintain a healthy environment for aquatic organisms.
Oxone (potassium monopersulfate) is sometimes used in the restoration and cleaning of artifacts, particularly those susceptible to damage from traditional cleaning methods.

In certain processes within the petroleum refining industry, Oxone (potassium monopersulfate) might be used for specific oxidation reactions.
Oxone (potassium monopersulfate) has been used in certain photographic developing processes due to its oxidizing properties.
Oxone (potassium monopersulfate) may be employed in biomedical research for specific laboratory procedures and experiments.

In fuel cell research, Oxone (potassium monopersulfate) might be used for its oxidizing capabilities in certain experimental setups.
Oxone (potassium monopersulfate) can be explored as a potential herbicide for weed control in agricultural settings.
Oxone (potassium monopersulfate) may find applications in aquariums for water treatment, helping to maintain a clean and safe environment for aquatic life.

In addition to the paper industry, Oxone (potassium monopersulfate) might be used in specific processes related to wood pulp processing.
Oxone (potassium monopersulfate) can be used for the cleaning and maintenance of plumbing systems, including the removal of biofilm and microbial growth.
Oxone (potassium monopersulfate) may be explored for certain pest control applications in agriculture, horticulture, or stored product protection.

Oxone (potassium monopersulfate) helps remove color from fabrics and paper products.
Oxone (potassium monopersulfate) is used in the hair dyeing industry to decolorize hair.
Oxone (potassium monopersulfate) is bleaching properties assist in the lightening or removal of hair color.

Oxone (potassium monopersulfate) serves as a powerful oxidizing agent in various chemical reactions and organic synthesis processes.
Oxone (potassium monopersulfate) can be used to oxidize organic compounds, initiating specific reactions.
Oxone (potassium monopersulfate) is applied in wastewater treatment to break down and remove organic pollutants.

Oxone (potassium monopersulfate) is strong oxidizing capabilities aid in the degradation of contaminants.
Oxone (potassium monopersulfate) is used for disinfection in spa and hot tub water.
Oxone (potassium monopersulfate) helps control the growth of bacteria and other microorganisms, particularly in warm water environments.

Oxone (potassium monopersulfate) can act as a polymerization initiator in certain polymerization reactions, contributing to the formation of polymers.
Oxone (potassium monopersulfate) is included in some household and industrial cleaning products for its disinfecting and cleaning properties.
Oxone (potassium monopersulfate) is used for halogenation of a,b-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.

Oxone (potassium monopersulfate) is a used for rapid, and good synthesis of oxaziridines.
Oxone (potassium monopersulfate) is used widely for cleaning.
Oxone (potassium monopersulfate) whitens dentures, oxidizes organic contaminants in swimming pools, and cleans chips for the manufacture of microelectronics.

Oxone (potassium monopersulfate) has been used for over 30 years in paper products such as tissue and towel paper, coffee filters and food packaging –
products that often come into close contact with humans, highlighting the need for a raw material that is safer for human health.
Oxone (potassium monopersulfate) is widely used in swimming pools and spas as an alternative to traditional chlorine-based treatments.
Oxone (potassium monopersulfate) helps oxidize impurities and eliminates bacteria, algae, and other microorganisms.

In these industries, Oxone (potassium monopersulfate) is employed as a bleaching agent.
Oxone (potassium monopersulfate) can bleach certain dyes and remove color from materials.
Oxone (potassium monopersulfate) is used in various chemical reactions where a strong oxidizing agent is required.

Oxone (potassium monopersulfate) is ability to provide active oxygen makes it useful in organic synthesis processes.
Oxone (potassium monopersulfate) is sometimes included in household cleaning products for its disinfecting and cleaning properties.
Oxone (potassium monopersulfate) is a potassium triple salt mainly used as a stable, easy to handle and nontoxic oxidant.

Oxone (potassium monopersulfate), monopersulfate compound may be used as an alternative to transition-metal oxidants for the conversion of aldehydes to carboxylic acids or esters.
Oxone (potassium monopersulfate) used for halogenation of α,β-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.
Oxone (potassium monopersulfate) is also used in direct and indirect oxidation techniques in metal extraction, ore separation, hydrometallurgy, and other surface treatments of metals and metal alloys like alloy formation, lamination, copper plating, final finish, and flash etch.

Oxone (potassium monopersulfate) functions for the destruction of cyanides as well as the oxidation of the various metals, including Chromium, Copper
Sulfide, Chalcopyrite, Cobalt, Nickel, and Manganese.
Most widely used in the oxidation of cyanide, reduced sulfur, and amine compounds, Oxone (potassium monopersulfate) provides safety and convenience in handling.

In oxidizing hydrogen sulfide (H2S) in waste streams, Oxone (potassium monopersulfate) allows for deodorizing a waste stream or stack via scrubbing without on-site manufacture or handling of hazardous ingredients like Caro's acid.
Analytical testing is still required to determine the effect on the waste stream to ensure complete removal of all compounds, including mercaptans, sulfides, disulfides, and sulfites.
Oxone (potassium monopersulfate) is used for shock treatment and as a non-chlorine alternative for oxidizing organic contaminants, bacteria, and algae in pool and spa water.

Employed in analytical chemistry for specific oxidation reactions and assays.
Oxone (potassium monopersulfate) is used in various laboratory experiments and procedures where a strong oxidizing agent is required.
Oxone (potassium monopersulfate) applied in certain environmental remediation processes to break down pollutants.

Oxone (potassium monopersulfate) used for halogenation of α,β-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.
Oxone (potassium monopersulfate), monopersulfate compound may be used as an alternative to transition-metal oxidants for the conversion of aldehydes to carboxylic acids or esters.
Oxone (potassium monopersulfate) used for halogenation of a,b-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.

Oxone (potassium monopersulfate) can be used in swimming pools to keep the water clear, thus allowing chlorine in pools to work to sanitize the water rather than clarify the water, resulting in less chlorine needed to keep pools clean.
One of the drawbacks of using Oxone in pools is it can cause the common DPD water test for combined chlorine to read incorrectly high.
Moreover, by-products can be formed during the peroxymonosulfate treatment, which are sometimes even more toxic than the original contaminants.

Oxone (potassium monopersulfate) is used in the formulations of Denture cleaners.
Oxone (potassium monopersulfate) is the effective main ingredient in Cleaning tablets for dentures.
Oxone (potassium monopersulfate) is used in disinfectants: Oxone is suitable for use for chlorine-free disinfection or purification of swimming pool water and spas.

Oxone (potassium monopersulfate) is a bleaching agent: Oxone (potassium monopersulfate) has a bleaching effect comparable to that of organic peracids
Oxone (potassium monopersulfate) has a biocidal effect: Oxone is suitable as an additive to acidic cleaning agents with bleaching and disinfectant effect.

Safety Profile:
Oxone (potassium monopersulfate) is a strong oxidizer and should be kept away from any reducing agents or organic compounds.
Oxone (potassium monopersulfate) can cause irritation to the skin and eyes. Direct contact with the skin or eyes may result in redness, itching, or discomfort.
Oxone (potassium monopersulfate)'s important to use appropriate personal protective equipment (PPE), such as gloves and goggles, when handling Oxone.

Oxone (potassium monopersulfate)'s recommended to use the chemical in well-ventilated areas, and respiratory protection may be necessary in situations where exposure to airborne particles is possible.
Ingesting Oxone can cause irritation to the gastrointestinal tract.
Accidental ingestion should be avoided, and immediate medical attention should be sought if ingestion occurs.

Some individuals may be allergic or sensitive to Oxone, leading to allergic reactions upon exposure.
If allergic reactions occur, medical attention should be sought.

Oxone (potassium monopersulfate) should be stored away from incompatible substances, as it can react with certain materials.
Common incompatible substances include reducing agents, strong acids, and some organic materials.



OXONE POTASSIUM MONOPERSULFATE
Oxone Potassium monopersulfate is a white, granular, free-flowing peroxygen powder that provides powerful non-chloride oxidation.
Oxone Potassium monopersulfate is the potassium salt of peroxymonosulfuric acid.


CAS Number: 70693-62-8
EC Number: 274-778-7
MDL Number: MFCD00040551
Molecular Fomula: 2KHSO5•KHSO4•K2SO4



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Oxone Potassium monopersulfate is a white, odourless, crystalline, free-flowing solid powder.
Oxone Potassium monopersulfate is a white powder and non-chlorine oxidizer, whose chemical formula is 2KHSO5•KHSO4•K2SO4.
Oxone Potassium monopersulfate is an odourless white powder that dissolves easily in water, sanitizing and improving water clarity without the carcinogenic trihalomethanes (THMs) that chlorine produces.


Oxone Potassium monopersulfate is ANSI60 certified for drinking water applications.
Oxone Potassium monopersulfate is abbreviated as PMs, which is a convenient, stable, and widely used inorganic acidic oxidant and disinfectant.
Oxone Potassium monopersulfate has strong non-chlorine oxidation ability, the product is safe and stable in solid state, easy to store, safe and convenient to use.


Oxone Potassium monopersulfate is a substance that can rapidly oxidize swimming pool .
Oxone Potassium monopersulfate is also called MPS, or Potassium peroxymonosulfate, as it is a potassium salt of peroxymonosulfuric acid.
Oxone Potassium monopersulfate is marketed as a popular non-chlorine based shock.


Oxone Potassium monopersulfate's primary swimming pool use is to oxidize any contaminates in the water, sanitizers already present in the water to focus on sanitizing the water.
Oxone Potassium monopersulfate is the first raw material verified for removal of wet strength resins in paper repulping.


Oxone Potassium monopersulfate is chlorine-free, meaning chlorine can be eliminated from the repulping process.
Oxone Potassium monopersulfate is extra pure an oxidizing agent.
Oxone Potassium monopersulfate is the potassium salt of peroxymonosulfuric acid.


Oxone Potassium monopersulfate is a white, odourless, crystalline, free-flowing solid powder.
Oxone Potassium monopersulfate decomposes when the temperature exceeds 60 degrees.
Oxone Potassium monopersulfate is highly soluble in water and slightly corrosive.


Oxone Potassium monopersulfate provides powerful non-chlorine oxidation and microbiological effectiveness for various industrial and consumer uses.
Oxone Potassium monopersulfate has the advantage of being highly stable in storage, easy and safe to handle.
Oxone Potassium monopersulfate does not contain chlorine, as it is a potassium salt of peroxymonosulfuric acid.


Oxone Potassium monopersulfate is marketed as a popular non-chlorine based shock.
Oxone Potassium monopersulfate's primary swimming pool use is to oxidize any contaminates in the water, leaving chlorine or bromine sanitizers already present in the water to focus on sanitizing the water.


Oxone Potassium monopersulfate is widely used as an oxidizing agent, for example, in pools and spas (usually referred to as monopersulfate or "MPS").
Oxone Potassium monopersulfate is the potassium salt of peroxymonosulfuric acid.
Oxone Potassium monopersulfate is a relatively obscure salt, but its derivative called Oxone Potassium monopersulfate is of commercial value.


Oxone Potassium monopersulfate refers to the triple salt 2KHSO5•KHSO4•K2SO4.
Oxone Potassium monopersulfate has a longer shelflife than does potassium peroxymonosulfate.
A white, water-soluble solid, Oxone Potassium monopersulfate loses <1% of its oxidizing power per month.


Oxone Potassium monopersulfate converts ketones to dioxiranes.
The synthesis of dimethyldioxirane (DMDO) from acetone is representative.
Dioxiranes are versatile oxidising agents and may be used for the epoxidation of olefins.


In particular, if the starting ketone is chiral then the epoxide may be generated enantioselectively, which forms the basis of the Shi epoxidation.
Oxone Potassium monopersulfate is a white, granular, free-flowing peroxygen powder that provides powerful non-chloride oxidation.
Oxone Potassium monopersulfate is the potassium salt of peroxymonosulfuric acid.


The active ingredient of Oxone Potassium monopersulfate is present as a component of a triple salt with the formula 2KHSO5•KHSO4•K2SO4 [potassium hydrogen peroxymonosulfate sulfate, [CAS-RN 70693-62-8].
The oxidation potential of Oxone Potassium monopersulfate is derived from its peracid chemistry; it is the first neutralization salt of peroxymonosulfuric acid H2SO5 (also known as Caro's acid).


Oxone Potassium monopersulfate is a highly active oxidant that is very effective at disinfecting swimming pools and lagoons.
Oxone Potassium monopersulfate's oxidation potential exceeds even that of hydrogen peroxide and ozone.
Potassium persulfate complex is an inorganic acidic oxidant, also known as potassium monopersulfate complex salt, potassium persulfate triplex salt peroxide potassium sulfate salt, is the common functional chemicals Oxone Potassium monopersulfate, Caroat, ZA200/100, Basolan2448 basic effective components.


Potassium monopersulfate, is a substance that can rapidly oxidize swimming pool .
Potassium monopersulfate is also called MPS, or Potassium peroxymonosulfate, as it is a potassium salt of peroxymonosulfuric acid.
Potassium peroxymonosulfate is marketed as a popular non-chlorine based shock.


Its primary swimming pool use is to oxidize any contaminates in the water, sanitizers already present in the water to focus on sanitizing the water.
Oxone Potassium monopersulfate is a non-chlorine shock.
Oxone Potassium monopersulfate will break the chlorine-ammonia bond formed when chlorine combines with ammonia, without increasing the chlorine level of the swimming pool.


Shocking is the introduction of a large amount of a chemical that causes contaminants in the pool to be oxidized (burned off).
The most common contaminant is chloramines, which is the combination of chlorine and ammonia.
These compounds are strong eye irritants and produce a strong chlorine odor.


They are eliminated by oxidation.
Oxidation can be accomplished by several means, the most common is the introduction of a chlorine shock, the second is non-chlorine shock.
Non-Chlorine shock provides tremendous versatility for pool and spa owners as well as pool professionals, Oxone Potassium monopersulfate is the oxidizer of choice, where the introduction of chlorine, which increases chlorine levels, may be irritating to some bathers.


Oxone Potassium monopersulfate is a white, free flowing crystalline granule, is non-toxic, odorless, and easily soluble in water.
Oxone Potassium monopersulfate is an efficient, environmentally friendly, and multifunctional acidic oxidant.
Oxone Potassium monopersulfate is a free-flowing, white granular solid, soluble in water.


Oxone Potassium monopersulfate is present as a component of a triple salt including potassium monopersulfate, potassium bisulfateand potassium sulfate with the formula 2KHSO5•KHSO4•K2SO4.
The oxidation potential of this compound is derived from its peracid chemistry.


Oxone Potassium monopersulfate has several important disadvantages and limitations.
While Oxone Potassium monopersulfate does oxidize and break down urea and chloramines, nitrate ions are the main oxidation product.
This is an important point to consider because like phosphates, nitrates are great algae food.


Furthermore, Oxone Potassium monopersulfate lowers the pH and the total alkalinity.
Oxone Potassium monopersulfate shows up as combined chlorine in the DPD test and as free chlorine in the FAS-DPD test.
Oxone Potassium monopersulfate oxidizes and reacts with one of the reagents.


This interference can be removed, however, and service technicians should be aware of this point.
Oxone Potassium monopersulfate is a strong oxidant with an oxidation potential of similar magnitude to that of chlorine.



USES and APPLICATIONS of OXONE POTASSIUM MONOPERSULFATE:
The use of Oxone Potassium monopersulfate has increased rapidly due to its inherent stability, the simple handling, the non-toxic nature, the versatility of the reagent and the relatively low cost.
Oxone Potassium monopersulfate is used for oral cleaning, swimming pool and hot spring water Disinfection, pulp bleaching.


Oxone Potassium monopersulfate provides powerful non-chlorine oxidation for a wide variety of industrial and consumer uses.
Oxone Potassium monopersulfate's applications may be found in oral hygiene formulations, pool and spa shock and disinfection, paper recycling, printed circuit board etching, wool shrink proofing, laundry bleaches, precious metal extraction process compounds, such as mercaptans, sulfides, disulfides, and sulfites in waste water treatment.


Oxone Potassium monopersulfate has been used for over 30 years in paper products such as tissue and towel paper, coffee filters and food packaging – products that often come into close contact with humans.
Oxone Potassium monopersulfate is used for halogenation of a,b-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.


Oxone Potassium monopersulfate is a used for rapid, and good synthesis of oxaziridines.
Oxone Potassium monopersulfate is used for halogenation of a,b-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.


Oxone Potassium monopersulfate is a reactive oxygen species (ROS) that has an inhibitory effect on the growth of bacteria.
Oxone Potassium monopersulfate is used as a disinfectant or sterilant and is often used in wastewater treatment plants to remove organic contaminants such as naphthalene.


Oxone Potassium monopersulfate's also an oxygen releasing agent in aquiculture and low temperature bleaching agent in detergent formulations.
Disinfectant uses of Oxone Potassium monopersulfate : In swimming pools and spas for the purpose of reducing the organic content of the water.
Printed Circuit Board Etching : Oxone Potassium monopersulfate is used as a micro-etching for cleaning and preparing copper printed wiring board surfaces.


Paper Recycling : Oxone Potassium monopersulfate is a convenient and effective processing aid for re-pulping wet strength resin or secondary fiber furnish.
Textile : Oxone Potassium monopersulfate is used as an oxidizer for the treatment of wool to prepare it for the application of shrink-proofing resins and laundry bleach.


Others uses of Oxone Potassium monopersulfate : Denture cleansers; Plaster Additive; Auxiliary Agent in organic synthesis; Carpet Browning and water decontamination.
Oxone Potassium monopersulfate is a stable, convenient and excellent acidity oxidant being widely used in the following industries; pool and spa, water disinfection, PCB etchant, pulp bleach, wool fabric shrink treatment agents, and metal refining agents.


The mechanism of action for Oxone Potassium monopersulfate involves its reaction with the electron-rich functional groups found on the bacterial cell membrane, which forms peroxides that cause irreversible damage to the cell.
Oxone Potassium monopersulfate also reacts with DNA, RNA, and proteins, and is therefore toxic to all cells.


Oxone Potassium monopersulfate has been shown to be effective against both Gram-positive and Gram-negative bacteria, but it does not work well against acid-fast bacteria such as Mycobacterium tuberculosis or Mycobacterium avium complex.
Oxone Potassium monopersulfate is used for halogenation of a,b-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.


Oxone Potassium monopersulfate is used for rapid, and good synthesis of oxaziridines
Oxone Potassium monopersulfate may be used as an alternative to transition-metal oxidants for the conversion of aldehydes to carboxylic acids or esters.
Oxone Potassium monopersulfate is also used to study fading of an artist′s colorants.


Oxone Potassium monopersulfate is a potassium triple salt mainly used as a stable, easy to handle and nontoxic oxidant.
Oxone Potassium monopersulfate is also used in organic synthesis, such as oxidizing the double bonds of organic molecules, or as an initiator in many radical polymerizations.


In addition, Oxone Potassium monopersulfate can oxidize the hydrogen sulfide or sulfur containing substances in wastewater, provide oxygen in aquaculture, and bleach to remove stains at a low temperature.
Oxone Potassium monopersulfate is used Oxidier Agent, Substitution for Halogen Oxidizer, and Enviromental Friendly.


Oxone Potassium monopersulfate is used in AquaculturePotassium Monopersulfate compound is a kind of acid oxidant, a free flowing white granularly powder, and soluble in water.
Oxone Potassium monopersulfate is a white, granular, free-fl owing peroxygen that provides powerful non-chlorine oxidation for a wide variety of uses.


Oxone Potassium monopersulfate is the active ingredient in most nonchlorine oxidizers used for pool and spa/hot tub oxidation.
Most non-chlorine oxidizers contain 45% of the active ingredient Oxone Potassium monopersulfate, but blended compositions are also commercially available that may contain buffers, clarifiers and/or additives for control of algae.


Oxone Potassium monopersulfate is not a sanitizer or algaecide and must be used in conjunction with an EPA-registered sanitizer.
The role of Oxone Potassium monopersulfate is to provide effective non-chlorine oxidation — in other words, to react with organic contaminants and maintain or restore water clarity.


Always follow label directions when using Oxone Potassium monopersulfate products to treat swimming pool and spa/hot tub water.
Oxone Potassium monopersulfate is compatible with all sanitizer products and systems.
When used with biguanide systems, follow the biguanide manufacturers’ specific recommendations for the use of pOxone Potassium monopersulfate.


It is recommended for use in indoor and outdoor residential and commercial venues.
While there is no specific test to determine when and how much Oxone Potassium monopersulfate should be applied, there are guidelines that can be followed to ensure proper use.


The primary parameters to be tested are free and combined chlorine.
Free chlorine should always be tested, and adjusted if necessary, to ensure proper sanitizer levels.
Testing combined chlorine indicates the level of contaminants bound to chlorine and the need for supplemental oxidation.


Pool and hot tub water should be properly balanced.
This requires testing of the pool water balance parameters of pH, carbonate alkalinity, calcium hardness, and stabilizer (i.e., cyanuric acid).
In addition, Oxone Potassium monopersulfate can be used as an oxidant for sulfur-containing substances such as hydrogen sulfide in wastewater treatment, a low-temperature oxygen-based bleach in detergent, and an oxygen supply agent in aquaculture.


Oxone Potassium monopersulfate can be used in animal breeding industry, cosmetics, daily chemicals, wool spinning and paper industry, water treatment industry, oil field, petrochemical, metal electroplating, smelting, printed circuit board PCB/metal surface treatment, chemical synthesis, etc.
Oxone Potassium monopersulfate's safe to use in a production facility, in the environment, and even as a key ingredient in your denture cleaner!


Oxone Potassium monopersulfate is used microetching and cleaning of printed wiring/circuit board (PWB)
For PWB industry, microetch solutions used to remove excess graphite and/or carbon black may be based on hydrogen peroxide or sodium persulfate as the oxidizing agent.


For example, a sodium persulfate-based product may be combined with sufficient sulfuric acid to make a microetch bath containing 100 300 grams of sodium persulfate per liter of deionized water and about 1 to 10% by weight sulfuric acid but nowadays, technical people find that Oxone Potassium monopersulfate could be used as very good solution as it contains required oxideizer, sulfuric acid as one step solution.


Key Applications of Oxone Potassium monopersulfate: Pool & Spa, Pulp & Paper, Electronics, Mining, Water Treatment, HI&I, Denture Cleaning.
Oxone Potassium monopersulfate is also used in organic synthesis, such as epoxidizing the double bonds of organic molecule, or as initiator in many radical polymerization.


In addition, Oxone Potassium monopersulfate can oxidize the hydrogen sulfide or sulfur-containing substances in the waster water, provide oxygen in aquaculture, and bleach to remove stains at low temperature.
Oxone Potassium monopersulfate is widely used in swimming pools to keep the water clear, thus allowing chlorine in pools to work to sanitize the water rather than clarify the water, resulting in less chlorine needed to keep pools clean.


Oxone Potassium monopersulfate is a popular choice is a non-chlorine product with potassium monopersulfate as the active ingredient.
Oxone Potassium monopersulfate is a powerful oxidizer with several attractive properties.
Properly applied, Oxone Potassium monopersulfate will prevent the formation of new combined chlorine by eliminating organics in the water without creating more combined chlorine.


Bathers can re-enter the water after waiting a short period of time (usually one hour) to allow proper mixing and circulation.
The reaction byproducts are harmless sulfate salts.
Oxone Potassium monopersulfate is a white granular product that provides non-chlorinated oxidation in a wide variety of applications.


Most notably, Oxone Potassium monopersulfate allows for efficient non-chlorinated oxidation as a pool shock, allowing less use of sanitizer and leaves the pool clean, clear, and swimmable nearly immediately.
The powerful oxidation as a microetchant in printed circuit boards improves process control in multi-step copper etching with a predictable rate to completion.


Oxone Potassium monopersulfate is of particular interest in metal plating and mining as it safely, economically, and conveniently oxidizes cyanide in waste streams.
In addition to testing the standard parameters, an overall assessment of pool and hot tub water and air quality should be performed.


Oxone Potassium monopersulfate has applications in denture cleansers, swimming pool oxidants, circuit board etchants, pulp recycling, wood cleaning and for other uses in which its combination of powerful oxidation and relative safety are useful.
Oxone Potassium monopersulfate is also known as MPS and it is widely used as an oxidizing agent.


Oxone Potassium monopersulfate is a stable, convenient, and widely used excellent acidic oxidant.
Oxone Potassium monopersulfate's application fields involve oral cleaning, swimming pool and hot spring water disinfection, Circuit board etchant, pulp bleaching, wool fabric anti-shrinkage treatment, precious metal extraction, etc.


Oxone Potassium monopersulfate salt is an important auxiliary agent in organic synthesis, which can epoxidize the double bonds in organic molecules.
Oxone Potassium monopersulfate is a free radical initiator for many polymerization reactions.
These key benefits of rapid rate of reaction as well as non-chlorinated oxidation has allowed repulping papers with wet strength resins to move their processes to greener methods without sacrificing production time.


Oxone Potassium monopersulfate is used to shock pools for a variety of reasons.
Some use Oxone Potassium monopersulfate to avoid using chlorine.
When chlorine is used to oxidize pool water, Oxone Potassium monopersulfate reacts with bather and other organic wastes, which are primarily nitrogen based compounds, to form chloramines.


These by-products have a foul odor and are considered unpleasant.
Oxone Potassium monopersulfate also reacts with the nitrogen- based compounds introduced by bathers, but because it does not contain chlorine, does not form chloramines in its oxidation process.


Also, Oxone Potassium monopersulfate dissolves quickly, and does not fade liners.
Oxone Potassium monopersulfate works well with chlorine, arguably allowing chlorine to work more efficiently as a sanitizer.
Using Oxone Potassium monopersulfate is highly recommended for indoor pools, where there is no sunlight or wind to help break down and carry away combined chlorine.


For indoor pools, shocking with Oxone Potassium monopersulfate is recommended about once a week.
For all its limitations, Oxone Potassium monopersulfate does have its uses.
The most important point to remember is that while it is certainly a strong oxidant, Oxone Potassium monopersulfate is NOT a sanitizer, and therefore provides no protection against bacteria and viruses.


Oxone Potassium monopersulfate, a stable, convenient and excellent acidity oxidant, is widely used in industries.
Oxone Potassium monopersulfate is used in oral hygiene, pool and spa waterdisinfection, PCB etchant, Pulp bleach, wool fabrics shrink treatment agent, precious metal refining agent.


-Water Balance uses of Oxone Potassium monopersulfate:
Regardless of the type of shock used, Oxone Potassium monopersulfate is important to maintain proper water balance to protect equipment and pool surfaces from corrosion and scaling.
Some shocks containing Oxone Potassium monopersulfate are acidic and periodic checking of the alkalinity and pH should be performed.
Oxone Potassium monopersulfate, does not contain calcium and hence will not increase calcium levels or cloud the water like some calcium based shocks


-Cleaning uses of Oxone Potassium monopersulfate:
Oxone Potassium monopersulfate is used widely for cleaning.
Oxone Potassium monopersulfate whitens dentures, oxidizes organic contaminants in swimming pools, and cleans chips for the manufacture of microelectronics.


-Organic chemistry uses of Oxone Potassium monopersulfate:
Oxone Potassium monopersulfate is a versatile oxidant in organic synthesis.
Oxone Potassium monopersulfate oxidizes aldehydes to carboxylic acids; in the presence of alcoholic solvents, the esters may be obtained.

Internal alkenes may be cleaved to two carboxylic acids (see below), while terminal alkenes may be epoxidized.
Sulfides give sulfones, tertiary amines give amine oxides, and phosphines give phosphine oxides.
Further illustrative of the oxidative power of this salt is the conversion of an acridine derivative to the corresponding acridine-N-oxide.
Oxone Potassium monopersulfate oxidizes sulfides to sulfoxides and then to sulfones.



BENEFITS OF OXONE POTASSIUM MONOPERSULFATE:
Oxone Potassium monopersulfate is a dynamic and potent biosecurity blend, effective against all types of pathogenic viruses, bacteria, fungi, and protozoa.
Oxone Potassium monopersulfate can potentially destroy many pathogens of economic importance in aquaculture farming.
Therefore, Oxone Potassium monopersulfate can reduce the incidence of disease outbreaks and enhance survivability.
Oxone Potassium monopersulfate is biodegradable, eco-friendly & safe for human and animal life.



PHYSICAL AND CHEMICAL PROPERTIES OF OXONE POTASSIUM MONOPERSULFATE:
Oxone Potassium monopersulfate has a very strong and effective non-chlorine oxidation ability, and the use and treatment process meets the requirements of safety and environmental protection.
Therefore, Oxone Potassium monopersulfate is widely used in industrial production and consumption.

In general, Oxone Potassium monopersulfate is relatively stable, and the decomposition reaction is easy to occur when the temperature is higher than 65.
More active, easy to participate in a variety of chemical reactions, Oxone Potassium monopersulfate can be used as oxidants, bleaching agents, catalysts, disinfectants, Etchants, etc.



ADVANTAGES OF OXONE POTASSIUM MONOPERSULFATE:
One of its greatest advantages is that bathers can reenter the water a short time after Oxone Potassium monopersulfate has been added - typically about 30 minutes.
Also, Oxone Potassium monopersulfate dissolves quickly, and does not fade liners, arguably allowing to work more efficiently as a sanitizer.

Using Oxone Potassium monopersulfate is highly recommended for indoor pools, where there is no sunlight or wind to help break down .
For indoor pools, shocking with Oxone Potassium monopersulfate is recommended about once a week.



PRODUCTION OF OXONE POTASSIUM MONOPERSULFATE:
Oxone Potassium monopersulfate is produced from peroxysulfuric acid, which is generated in situ by combining oleum and hydrogen peroxide.
Careful neutralization of this solution with potassium hydroxide allows the crystallization of the triple salt.



SWIMMING POOL SHOCK AND SPA, OXONE POTASSIUM MONOPERSULFATE:
Oxone Potassium monopersulfate can be added to pool water day or night, and swimming caroat, Oxone Potassium monopersulfate, virkon can resume after a short waiting period to allow for adequate mixing and dispersion throughout the pool.
No mixing is required; Oxone Potassium monopersulfate is completely soluble in water and dissolves quickly.

Broadcast monopersulfate shock slowly and uniformly over the surface of the water, adding about two-thirds of the total dose over the deep end.
Shock with the filter running to ensure complete mixing and good circulation.
Oxone Potassium monopersulfate is a versatile oxidant.

Oxone Potassium monopersulfate oxidizes aldehydes to carboxylic acids; in the presence of alcoholic solvents, the esters may be obtained.
Internal alkenes may be cleaved to two carboxylic acids, while terminal alkenes may be epoxidized.
Thioethers give sulfones, tertiary amines give amine oxides, and phosphines give phosphine oxides.

Oxone Potassium monopersulfate will also oxidize a thioether to a sulfone with 2 equivalents.
With one equivalent the reaction converting sulfide to sulfoxide is much faster than that of sulfoxide to sulfone, so the reaction can conveniently be stopped at that stage if so desired.



THE ADVANTAGES OF USING OXONE POTASSIUM MONOPERSULFATE IN SWIMMING POOLS TREATMENT:
*Maximum disinfection efficiency caused by oxidizing properties,
*Restores water cleanliness and transparency,
*Suitable for all types of swimming pools, spas, bathtubs,
*Significantly improves chlorination efficiency through quick oxidization of organic contaminants,
*Very quick action – facility is ready to use after 15 minutes,
*Harmless to swimming pool surfaces, causes no bleaching or discolouration of painted and vinyl-coated surfaces,
*No irritating odour, does not cause allergy as Oxone Potassium monopersulfate contains no chloride, aldehydes, alcohol,
*Oxone Potassium monopersulfate has no impact on water hardness.



PRODUCTION SITE OF OXONE POTASSIUM MONOPERSULFATE:
Oxone Potassium monopersulfate provides powerful non-chlorine oxidation for a wide variety of industrial and consumer uses.
Oxone Potassium monopersulfate’s applications may be found in oral hygiene formulations, pool and spa shock and disinfections, paper recycling, printed circuit board etching, wool shrink proofing, laundry bleaches, precious metal extraction process.

Oxone Potassium monopersulfate is an important auxiliary agent in organic synthesis for oxidizing plenty of organics and functioning as the epoxy oxidizer of the twin bonds of organic chemicals.
Oxone Potassium monopersulfate’s also a free radicle introductory agent in many polymeric reactions.

Oxone Potassium monopersulfate can be used to oxidize hydrogen sulfide (H2S) and other reduced sulfur compounds, such as mercaptans, sulfides, disulfides, and sulfites in waste water treatment.
Oxone Potassium monopersulfate’s also an oxygen releasing agent in aquiculture and low temperature bleaching agent in detergent formulations.



THE BEAUTY OF OXONE POTASSIUM MONOPERSULFATE:
There are some who have turned to Oxone Potassium monopersulfate as a means for shocking their pools. KMPS is a non-chlorine oxidizer, whose chemical formula is KHSO5.
Oxone Potassium monopersulfate is a strong oxidant with an oxidation potential of similar magnitude to that of chlorine.
While Oxone Potassium monopersulfate is a powerful oxidizer, there are several important points to consider about this chemical.



WOOL SHRINKPROOFING OF OXONE POTASSIUM MONOPERSULFATE:
Oxone Potassium monopersulfate is more commonly known name as an oxidizer for wool shrinkproofing treatment.
Oxone Potassium monopersulfate is in the form of a granule, easily dissolved, and an aqueous solution contains the dissolved oxidizer is stable for sotrage at a temperature of 32 centigrade. a -S--S-bond is stopped at substantially mono-oxidized state.

Oxone Potassium monopersulfate is used odor control agent in wastewater treatment
Oxone Potassium monopersulfate is used bleach component in denture cleanser and laundry formulations
Oxone Potassium monopersulfate is used activator in antimicrobial compositions
Other uses of Oxone Potassium monopersulfate where its combination of powerful oxidation and relative.



PHYSICAL and CHEMICAL PROPERTIES of OXONE POTASSIUM MONOPERSULFATE:
Molecular weight: 614.7
Appearance: White, free flowing granule
Available Oxygen, % =4.5
KHSO5, %=42.8
Loss on Drying, %=0.15
Bulk Density, g/L=0.80
pH (10g/L,25C): 2.0~2.4
Sieve Residue on 75m test sieve: =90.0
Chemical formula: KHSO5
Molar mass: 152.2 g/mol (614.76 g/mol as triple salt)
Appearance: Off-white powder
Solubility in water: Decomposes
Physical state: granular

Color: white
Odor: none
Melting point/freezing point:
Melting point/range: Decomposes before melting.
Initial boiling point and boiling range: Not applicable
Flammability (solid, gas): The product itself does not burn,
but it is slightly oxidizing
(active oxygen content ca. 2%).
Upper/lower flammability or explosive limits: No data available
Flash point: does not flashNot applicable
Autoignition temperature: Not applicable
Decomposition temperature: No data available
pH: 2,1 at 30 g/l at 77 °C

Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility 357 g/l at 22 °C - soluble
Partition coefficient: n-octanol/water: No data available
Vapor pressure: < 0,0000017 hPa
Density: 1,100 - 1,400 g/cm3
Relative density: 2,35 at 20 °C
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: Not classified as explosive.
Oxidizing properties: The substance or mixture is not classified as oxidizing.

Other safety information:
Bulk density 1.100 - 1.400 kg/m3
APPEARANCE: WHITE POWDER OR GRANULE
ACTIVE OXYGEN%: ≧4.50
ACTIVE COMPONENT(KHSO5)%: ≧42.80
WATER SOLUBILITY(G/L20C): 256
MOISTURE%: ≤0.1
BULKDENSITYG/CM*3: 1.00-1.30
PHTEST(10G/L,25C): 2.0-2.3
PARTICALSIZE(20-200MESH): ≧90.0
CAS: 70693-62-8
EINECS: 274-778-7

InChI: InChI=1/K.H2O6S/c;1-5-6-7(2,3)4/h;1H,(H,2,3,4)/q+1;/p-1/rHKO6S/c1-5-6-7-8(2,3)4/h(H,2,3,4)
InChIKey: HVAHYVDBVDILBL-UHFFFAOYSA-M
Molecular Formula: HKO6S
Molar Mass: 168.17
Density: 1.15
Melting Point: 93℃
Water Solubility: Soluble in water (100 mg/ml).
Solubility: 250-300g/l soluble
Appearance: White crystalline powder
Specific Gravity: 1.12-1.20
Color: white
Exposure Limit ACGIH: TWA 0.1 mg/m3
PH: 2-3 (10g/l, H2O, 20℃)

Storage Condition: Store at <= 20°C.
Stability: Stable.
Sensitive: Hygroscopic
MDL: MFCD00040551
Appearance: free-flowing granule
KHSO5, %: ≥42.8
Active Component (KHSO5.KHSO4.K2SO4), %: ≥99
Moisture, %: ≤0.5
Bulk Density, g/L: 800-1200
pH(1%suspension): 2.0~2.3
Particle Size Distribution(0.850~0.075mm),%: ≥90.0
Stability ,active oxygen loss/month, %: ≤1.0
Solubility(20ºC,100g water),g: ≥14.5
CAS: 70693-62-8
EINECS: 274-778-7
InChI: InChI=1/K.H2O6S/c;1-5-6-7(2,3)4/h;1H,(H,2,3,4)/q+1;/p-1/rHKO6S/c1-5-6-7-8(2,3)4/h(H,2,3,4)
InChIKey: HVAHYVDBVDILBL-UHFFFAOYSA-M

Molecular Formula: HKO6S
Molar Mass: 168.17
Density: 1.15
Melting Point: 93℃
Water Solubility: Soluble in water (100 mg/ml).
Solubility: 250-300g/l soluble
Appearance: White crystalline powder
Specific Gravity: 1.12-1.20
Color: white
Exposure Limit ACGIH: TWA 0.1 mg/m3
PH: 2-3 (10g/l, H2O, 20℃)
Storage Condition: Store at <= 20°C.
Stability: Stable.
Sensitive: Hygroscopic
MDL: MFCD00040551



FIRST AID MEASURES of OXONE POTASSIUM MONOPERSULFATE:
-Description of first-aid measures:
*General advice:
First aiders need to protect themselves.
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
Call in physician.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Call a physician immediately.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Immediately call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Make victim drink water (two glasses at most).
Call a physician immediately.
Do not attempt to neutralise.
-Indication of any immediate medical attention and special treatment needed
No data available



ACCIDENTAL RELEASE MEASURES of OXONE POTASSIUM MONOPERSULFATE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of OXONE POTASSIUM MONOPERSULFATE:
-Extinguishing media:
*Suitable extinguishing media:
Use extinguishing measures that are appropriate to local circumstances and the surrounding environment.
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Suppress (knock down) gases/vapors/mists with a water spray jet.
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of OXONE POTASSIUM MONOPERSULFATE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
Acid-resistant protective clothing
*Respiratory protection:
Recommended Filter type: Filter type P2
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of OXONE POTASSIUM MONOPERSULFATE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
hygroscopic
*Storage class:
Storage class (TRGS 510): 8B:
Non-combustible



STABILITY and REACTIVITY of OXONE POTASSIUM MONOPERSULFATE:
-Reactivity:
No data available
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available



Oxybenzone
cas no 144-62-7 (Anhydrous) 6153-56-6 (Dihydrate) Ethanedioic acid, dihydrate; Oxaalzuur (Dutch)Oxalsäure (German); ácido oxálico (Spanish); Acide oxalique (French); Kyselina stavelova (Czech);
PAC (Polyaluminium Chlorohydrate)
Polyaluminum chlorohydrate; Polyaluminum hydroxychloride CAS NO:1327-41-9
PALATINOL IC
Palatinol IC is an odorless plasticizer with the molecular formula C16H22O4.
Palatinol IC is a phthalate ester that is the diester obtained by the formal condensation of the carboxy groups of phthalic acid with two molecules of isobutanol.
Palatinol IC belongs to the class of organic compounds known as benzoic acid esters.

CAS Number: 84-69-5
EC Number: 201-553-2
Chemical formula: C16H22O4
Molar mass: 278.348 g·mol−1

Synonyms: Bis(2-methylpropyl) benzene-1,2-dicarboxylate, Diisobutyl phthalate, Di-iso-butyl phthalate, Di(i-butyl)phthalate, Diisobutyl ester of phthalic acid, 1,2-benzenedicarboxylic acid, Bis(2-methylpropyl)ester, Di(isobutyl) 1,2-benzenedicarboxylate, Isobutyl-O-phthalate, DIBP, DiBP, Palatinol IC, DIISOBUTYL PHTHALATE, 84-69-5, DIBP, Palatinol IC, Isobutyl phthalate, Phthalic Acid Diisobutyl Ester, Hexaplas M/1B, Kodaflex DIBP, Di-iso-butyl phthalate, Phthalic acid, diisobutyl ester, Di(i-butyl)phthalate, 1,2-Benzenedicarboxylic acid, bis(2-methylpropyl) ester, Diisobutylester kyseliny ftalove, NSC 15316, bis(2-methylpropyl) phthalate, isobutyl-o-phthalate, 1,2-Benzenedicarboxylic acid, 1,2-bis(2-methylpropyl) ester, DTXSID9022522, di-2-methylpropyl phthalate, di-l-butyl phthalate (DIBP), IZ67FTN290, CHEBI:79053, NSC-15316, Hatcol DIBP, DTXCID602522, 1,2-benzenedicarboxylic acid bis(2-methylpropyl) ester, 1,2-Benzenedicarboxylic acid, di(2-methylpropyl) ester, Phthalic acid, bis-isobutyl ester, CAS-84-69-5, SMR000112470, di-isobutyl phthalate, CCRIS 6193, HSDB 5247, AI3-04278 (USDA), EINECS 201-553-2, BRN 2054802, UNII-IZ67FTN290, AI3-04278, Isobutyl phthalate (VAN), bis(2-methylpropyl) benzene-1,2-dicarboxylate, EC 201-553-2, Diisobutyl phthalate, 99%, SCHEMBL42787, 4-09-00-03177 (Beilstein Handbook Reference), MLS000516002, MLS002152902, BIDD:ER0640, 1, bis(2-methylpropyl) ester, CHEMBL1370662, HMS2269D07, NSC15316, Tox21_202429, Tox21_300612, MFCD00026480, AKOS015837516, Diisobutyl phthalate (ACD/Name 4.0), WLN: 1Y1&1OVR BVO1Y1&1, NCGC00091360-01, NCGC00091360-02, NCGC00091360-03, NCGC00091360-04, NCGC00254487-01, NCGC00259978-01, FT-0689059, NS00010605, P0298, Q162259, 1,2-bis(2-methylpropyl) benzene-1,2-dicarboxylate, J-503794, 1,2-benzenedicarboxylic acid di(2-methylpropyl) ester, Phthalic acid, bis-isobutyl ester 10 microg/mL in Cyclohexane, Diisobutyl phthalate, certified reference material, TraceCERT(R), 1,2-Benzenedicarboxylic acid, bis(2-methylpropyl) ester, DIBP, Di(i-butyl)phthalate, Di-iso-butyl phthalate, Diisobutylester kyseliny ftalove [Czech], Hatcol DIBP, Hexaplas M/1B, Isobutyl phthalate, Kodaflex DIBP, Palatinol IC, Phthalic acid, diisobutyl ester, Phthaloyl dichloride, MFCD01861606, EINECS 201-553-2, Phthalyl chloride, bis(2-methylpropyl) benzene-1,2-dicarboxylate, Phthalic dichloride, 1,2-Benzenedicarbonyl dichloride, tetraphthaloyl chloride, Phthalic acid dichloride, diisobutyl 1,2-benzenedicarboxylate, 1,2-Benzenedicarboxylic acid, bis(2-methylpropyl) ester, di-l-butyl phthalate (DIBP), Diisobutyl phthalate, phthaloyl chloride, Phthalyl dichloride, benzene-1,2-dicarbonyl dichloride, Phthalic chloride, 1,2-benzene dicarboxylic acid diisobutyl ester, 1,2-benzenedicarboxylic acid, bis(2-methylpropyl) ester, AI3-04278, bisoflex DIBA, bisoflex DIBP, di(isobutyl) 1,2-benzenedicarboxylate, DIBP (=diisobutyl phthalate), diplast B, hatcol DIBP, hexaplas M 18, hexaplas M/1B, hexaplas MIB, isobutyl phthalate, jayflex DIBP, kodaflex DIBP, mollan L, phthalic acid diisobutyl ester, vestinol IB), DBP, ARALDITE RESIN, Butyl phthalate, N-BUTYL PHTHALATE, Dibutyl phthalate, Dibutyl-o-phthalate, Di-n-butyl phthalate, Dibutyl Phthalate(DBP), Diisobutyl Phthalate(DIBP), PHTHALIC ACID DIBUTYL ESTER, Phthalic acid di-n-butyl ester, Dibutyl phthalate,abbreviation, PHTHALIC ACID DI-N-BUTYL ESTER, PHTHALIC ACID, BIS-BUTYL ESTER, dibutyl benzene-1,2-dicarboxylate, O-BENZENEDICARBOXYLIC ACID DIBUTYL ESTER, Benzene-1,2-dicarboxylic acid di-n-butylester, 1,2-Benzenedicarboxylic acid, 1,2-bis(2-methylpropyl) ester, 1,2-Benzenedicarboxylic acid, bis(2-methylpropyl) ester, 1,2-Benzenedicarboxylic acid, di(2-methylpropyl) ester, Bis(2-methylpropyl) phthalate, Di-2-methylpropyl phthalate, DIBP, Diisobutyl phthalic acid, Hexaplas M/1B, Isobutyl phthalate,

Palatinol IC is an organic compound used as a plasticizer in the production of plastic and rubber.
Palatinol IC is a colorless, oily liquid with a slight odor.

Palatinol IC is a phthalate ester, which is a type of chemical compound derived from phthalic acid.
Palatinol IC is a clear liquid.

Palatinol IC is a colorless oily liquid with a slight ester odor.
Palatinol IC is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 tonnes per annum.

Palatinol IC is a phthalate ester that is the diester obtained by the formal condensation of the carboxy groups of phthalic acid with two molecules of isobutanol.
Palatinol IC is oily colorless liquid with a slight ester odor.

Palatinol IC is an odorless plasticizer with the molecular formula C16H22O4.
Palatinol IC is a phthalate ester that is the diester obtained by the formal condensation of the carboxy groups of phthalic acid with two molecules of isobutanol.

Palatinol IC is soluble in ethanol, ether, acetone and benzene.
Palatinol IC belongs to the class of organic compounds known as benzoic acid esters.
These are ester derivatives of benzoic acid.

Palatinol IC is prepared by esterification process of isobutanol and phthalic anhydride.
Palatinol IC is an odorless plasticizer and has excellent heat and light stability.

Palatinol IC is the lowest cost plasticizer for cellulose nitrate.
Palatinol IC has lower density and freezing point than DBP.

Palatinol IC has similar properties as dibutyl phthalate and can be used as a substitute for it.
Palatinol IC is an oily colorless liquid with a slight ester odor.

Palatinol IC is denser than water.
Palatinol IC is insoluble in water.

Palatinol IC is a phthalate ester that is the diester obtained by the formal condensation of the carboxy groups of phthalic acid with two molecules of isobutanol.
Palatinol IC has a role as a plasticiser, a teratogenic agent and a PPAR modulator.

Palatinol IC is a phthalate ester and a diester.
Palatinol IC is functionally related to an isobutanol.

Palatinol IC is an odorless plasticizer and has excellent heat and light stability.
Palatinol IC is the lowest cost plasticizer for cellulose nitrate.
Palatinol IC has lower density and freezing point than DBP (dibutyl phthalate, CAS No.: 84-74-2).

Palatinol IC can substitute dibutyl phthalate (DBP) in most, if not all, applications.
Since Palatinol IC is not chemically bound in the polymer matrix it may outgas or be released upon contact with fluids and fat.
In the environment Palatinol IC is degraded relatively fast.

Palatinol IC is compatible with PVC.
Palatinol IC is a phthalate ester having the structural formula C6H4(COOCH2CH(CH3)2)2.

Palatinol IC is formed by the esterification of isobutanol and phthalic anhydride.
When it comes to excretion, Palatinol IC is first converted into the hydrolytic monoester monoisobutyl phthalate (MIBP).

The primary excretory route is urine, with biliary excretion being noted in minor amounts.
Palatinol IC has lower density and freezing point than the related compound dibutyl phthalate (DBP).

Palatinol IC can be sold as a pure substance or as a component of mixtures with other phthalate plasticizers or chemicals.
Examples are dioctyl phthalate (DOP), diisononyl-phthalate (DINP), or bis(2-ethylhexyl) phthalate (DEHP).
Palatinol IC is a natural product found in Artemisia baldshuanica, Lythrum salicaria, and other organisms with data available.

Uses of Palatinol IC:
Palatinol IC is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Palatinol IC is used in the following products: coating products, fillers, putties, plasters, modelling clay and polymers.

Other release to the environment of Palatinol IC is likely to occur from: indoor use and outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives).
Release to the environment of Palatinol IC can occur from industrial use: in the production of articles, formulation of mixtures and of substances in closed systems with minimal release.
Other release to the environment of Palatinol IC is likely to occur from: indoor use, outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives), outdoor use in long-life materials with high release rate (e.g. tyres, treated wooden products, treated textile and fabric, brake pads in trucks or cars, sanding of buildings (bridges, facades) or vehicles (ships)) and indoor use in long-life materials with high release rate (e.g. release from fabrics, textiles during washing, removal of indoor paints).

Palatinol IC can be found in complex articles, with no release intended: vehicles, machinery, mechanical appliances and electrical/electronic products (e.g. computers, cameras, lamps, refrigerators, washing machines) and electrical batteries and accumulators.
Palatinol IC can be found in products with material based on: plastic (e.g. food packaging and storage, toys, mobile phones), metal (e.g. cutlery, pots, toys, jewellery), rubber (e.g. tyres, shoes, toys), leather (e.g. gloves, shoes, purses, furniture) and wood (e.g. floors, furniture, toys).

Palatinol IC is used in the following products: coating products, fillers, putties, plasters, modelling clay, polymers and adhesives and sealants.
Palatinol IC is used in the following areas: formulation of mixtures and/or re-packaging.

Palatinol IC is used for the manufacture of: plastic products, mineral products (e.g. plasters, cement) and machinery and vehicles.
Release to the environment of Palatinol IC can occur from industrial use: in the production of articles, of substances in closed systems with minimal release and industrial abrasion processing with low release rate (e.g. cutting of textile, cutting, machining or grinding of metal).

Other release to the environment of Palatinol IC is likely to occur from: indoor use and outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives).
Palatinol IC is used in the following products: coating products, fillers, putties, plasters, modelling clay and polymers.

Palatinol IC has an industrial use resulting in manufacture of another substance (use of intermediates).
Release to the environment of Palatinol IC can occur from industrial use: formulation of mixtures and formulation in materials.
Palatinol IC has an industrial use resulting in manufacture of another substance (use of intermediates).

Palatinol IC is used in the following areas: formulation of mixtures and/or re-packaging.
Palatinol IC is used for the manufacture of: chemicals.
Release to the environment of Palatinol IC can occur from industrial use: as an intermediate step in further manufacturing of another substance (use of intermediates) and in the production of articles.

Release to the environment of Palatinol IC can occur from industrial use: manufacturing of Palatinol IC.
Palatinol IC is a plasticizer in used in consumer
products as a substitute ingredient to di-n-butyl phthalate (DBP) due to structural similarities.

Therefore, Palatinol IC's presence in products may increase.
Palatinol IC is a plasticizer used in poly-vinyl chloride (PVC) plastic to increase flexibility.

Palatinol IC can be used replacement for dibutyl phthalate due to lower production costs.
Additionally, Palatinol IC can be used in applications such as ink, coatings, lacquers, and adhesives.

Palatinol IC acts as a plasticizer.
Palatinol IC can be used as a replacement for dibutyl phthalate due to lower production costs.

Palatinol IC is used in poly-vinyl chloride (PVC) plastic to increase flexibility.
Palatinol IC is used as plasticizer.

Palatinol IC is used in paints, lacquers, and varnishes.
Palatinol IC is also used in the paper and pulp industry and to make boards, chemicals, polymers, adhesives, softeners, and viscosity adjusters.

Palatinol IC is prepared by esterification process of isobutanol and phthalic anhydride.
Palatinol IC is an odorless plasticizer and has excellent heat and light stability.

Palatinol IC is the lowest cost plasticizer for cellulose nitrate.
Palatinol IC has lower density and freezing point than DBP.

Palatinol IC has similar properties as dibutyl phthalate and can be used as a substitute for it.
Palatinol IC is a colorless transparent oily liquid used as an alternative to DBP (Dibutyl Phthalate).

Palatinol IC is used in nitrocellulose and alkyd resin paints.
Palatinol IC is prepared by esterification process of isobutanol and phthalic anhydride.

Palatinol IC is an odorless plasticizer and has excellent heat and light stability.
Palatinol IC is the lowest cost plasticizer for cellulose nitrate.

Palatinol IC has lower density and freezing point than DBP.
Palatinol IC has similar properties as dibutyl phthalate and can be used as a substitute for it.

Palatinol IC is a plasticizer that is used in nitrocellulose, alkyd resin paints, inks, coatings, lacquers, and adhesives.
Due to lower production costs, Palatinol IC is used as an alternative to DBP (Dibutyl Phthalate).

Palatinol IC is a plasticizer that is used with different polymers such as polyacrylate, poly acetate dispersions, cellulose acetate, nitrocellulose, polyurethane, and polyvinyl butyrate.
Palatinol IC often is used in combination with other phthalates.

Palatinol IC is used most of the time as a substitute for DBP.
Palatinol IC is used in the plasticization of PVC, the production of paints, printing inks, and adhesives.

Some of Palatinol IC uses include: Floorings, Paints, Industrial adhesives, Lacquers, Printing inks, Hydraulic fluids, and Lubricants.
Palatinol IC is used in a variety of products, including food packaging, medical devices, and toys.

Palatinol IC is used as a plasticizer in the manufacture of flexible PVC products, such as wire and cable insulation, vinyl flooring, adhesives, and coatings.
Palatinol IC is also used in the production of lacquers, printing inks, and synthetic leather.

Palatinol IC is a Dialkyl phthalate ester phthalate plasticizer which can be used as a substitute of dibutyl phthalate.
Palatinol IC as well as other phthalates have genotoxic effects and studies shown an increase in its monoester metabolite in human urine over the years.

Palatinol IC is one of the main plasticizers in common use.
Palatinol IC can be used as plasticizer of cellulose resin, vinyl resin, NBR and chlorinated rubber.

Similar to Palatinol IC, it has excellent solubility, dispersibility and adhesion.
Palatinol IC has good compatibility with pigment.

Palatinol IC can be used for coloring film, artificial leather and plastic products.
Palatinol IC can also be used as softener of natural rubber and synthetic rubber to improve the resilience of products.

Palatinol IC can be used as a substitute for DBP.
Palatinol IC is a phthalate ester that is the diester obtained by the formal condensation of the carboxy groups of phthalic acid with two molecules of isobutanol Palatinol IC is considered a specialty plasticizer that is too volatile for use in polyvinyl chloride (PVC).

Palatinol IC is often combined with other phthalates.
Palatinol IC has good heat and light stability and has been used as a plasticizer for nitrocellulose (lowest cost plasticizer for cellulose nitrate), cellulose ether, and polyacrylate and polyacetate dispersions.

Palatinol IC is used in nail polish, cosmetics, lubricants, floor carpets, tapestry, clothing treatments, rubber dentistry settings, as a fuel stabilizer, in leather varnishes and lacquers, as a concrete additive, as an adjusting agent for lead chromate paint pigments, explosive material, lacquer manufacturing, and methyl methacrylate applications.

Palatinol IC is also used in printing inks for paper and packaging.
Because Palatinol IC has similar properties as dibutyl phthalate (DBP), Palatinol ICcan be used as a substitute for DBP.

Palatinol IC is mainly used as nitrocellulose, cellulose acetate, polyvinyl chloride and other plasticizers; General Chemical analysis reagents for gas chromatography stationary liquid.
Palatinol IC is used as solvents, pesticides, plasticizers.

Palatinol IC has similar properties as dibutyl phthalate and can be used as a substitute for it.
Palatinol IC is synthesized by chemical reaction of phthalic acid with iso-butyl alcohol.

Palatinol IC is a plasticizer with coagulating properties which was used with different polymers, e.g. poly acrylate, poly acetate dispersions, cellulose acetate, cellulose nitrate, ethyl cellulose, polyurethane, and polyvinyl butyrate.
In combination with other plasticizers Palatinol IC was applied as gellant in processing of so-called plastisols.

Palatinol IC is present for instance in floorings, adhesives, lacquers, inks, hydraulic fluids and lubricants.
Palatinol IC was used as marker in fuels for tax purposes and also in the production of titanium catalysers.
Palatinol IC can be used as a replacement for dibutyl phthalate due to lower production costs.

Palatinol IC is used in adhesives.
Palatinol IC may be used as a component in formulations of several products including adhesives, paints, coatings and lubricants.

This and other phthalates are used as plasticizers due to their flexibility and durability.
They are found in many industrial and personal products, such as lacquers, nail polish and cosmetics.

Industry uses:
Palatinol IC is used as a plasticizer additive in a range of plastic and rubber materials.
Palatinol IC has low volatility, which makes it ideal for use in products that require long-lasting flexibility, e.g. automotive parts, wire and cable insulation, and flooring.
Palatinol IC is dense and water-insoluble.

Food Industry:
Palatinol IC is used as a plasticizer in food packaging materials, such as polyvinyl chloride (PVC) films and sheets.
Palatinol IC is also used in food contact materials, such as adhesives, coatings, and sealants.
Palatinol IC is used to improve the flexibility, durability, and transparency of these materials.

Production Method of Palatinol IC:
Palatinol IC is manufactured by esterifying phthalic anhydride and isobutanol in the presence of sulfuric acid.
Palatinol IC is synthesized by the esterification process of isobutanol and phthalic anhydride in the presence of sulphuric acid as a catalyst.

Synthesis of Palatinol IC:
Palatinol IC is synthesized by a double nucleophilic acyl substitution reaction between phthalic anhydride and isobutanol, using various acids as a catalyst, such as sulfuric acid, sulfonated graphene, or iron(III) chloride.
Water is a byproduct.
Using sulfuric acid, the yield is 61% yield.

Optimization of Palatinol IC:
Sulfonated graphene is a heterogeneous catalyst that has several advantages over traditional liquid acids like sulfuric acid.
Sulfonated graphene can be easily separated from the reaction mixture by filtration and can be reused multiple times without reduction in activity.

Furthermore, sulfonated graphene is environmentally friendly, as Palatinol ICdoes not produce hazardous waste materials that are typically generated during the use of traditional liquid acid catalysts.
This method has a 95% yield.

Lewis acids, such as FeCl3, can also be used as the catalyst.
The Lewis acid catalysis process can be run at lower temperatures (50-100 °C), and gives a yield of 86%.

Actions Mechanism of Palatinol IC:

PPARγ Pathway:
The effects of Palatinol IC exposure are mainly realized through its activation of peroxisome proliferator-activated receptor gamma (PPARγ).
PPARs are ligand-activated nuclear transcription factors, the family consists of PPARα, PPARβ/δ and PPARγ.
There are two isoforms of PPARγ, PPARγ2 is mainly present on cells in adipose tissue, whereas PPARγ1 is found on multiple cells like those in the gut, brain, blood vessels, and some immune and inflammatory cells.

Transcriptional regulation through PPARs requires the formation of a heterodimer with retinoid X receptor (RXR).
Upon activation by Palatinol IC this PPARγ/RXR heterodimer binds to a DNA sequence called the PPAR response element (PPRE).
Binding of the transcription factor to this response element can result in either up- or down-regulation of genes.

PPARγ is involved in lipid metabolism and storage as well as glucose metabolism through improving insulin sensitivity, so binding of Palatinol IC leads to altered leptin and insulin levels.
Palatinol IC also leads to a down-regulation of proteins involved in steroid production, resulting in higher levels of androgenic hormones.

Cytokine-cytokine receptor pathway
Another type of pathway affected by Palatinol IC exposure is the cytokine-cytokine receptor pathway.
There are two pathways affected: the tumour necrosis factor receptor superfamily (TNFRSF) and the prolactin receptor pathway, both of which affect spermatogenesis.

Environmental Reactions of Palatinol IC:
Palatinol IC can undergo various reactions that may impact the environment

Examples include:

Hydrolysis:
Hydrolyzation of Palatinol IC can be done by enzymes, bacteria, and other microorganisms in the environment to form phthalic acid and isobutyl alcohol.
This can lead to the breakdown and the eventual degradation of Palatinol IC in the soil and water supply

Photodegradation:
Palatinol IC can undergo photodegradation by exposure to the sunlight.
This can lead to the formation of several degradation products, including phthalic acid, isobutyraldehyde, and other aldehydes.

Biodegradation:
Palatinol IC can be degraded by microorganisms in soil and in the water.
This can transform Palatinol IC into other compounds such as phthalic acid and various isobutyl alcohol derivatives.

Sorption:
Palatinol IC can adsorb or sorb onto soil and sediment particles, which can limit Palatinol IC mobility and availability for biological or chemical degradations and reactions.

Oxidation:
Palatinol IC can be oxidized in the presence of ozone or other reactive oxygen species.
The formation of various oxidation products, including aldehydes, ketones, and carboxylic acids can be expected.
These reactions can impact the persistence, bioaccumulation, and toxicity in the environment and may have implications for human and ecosystem health.

Matebolism of Palatinol IC:
Upon entering circulation Palatinol IC is quickly metabolized and excreted through urine, with metabolites reaching peak concentrations 2–4 hours after administration.
The main metabolite of Palatinol IC is mono-isobutyl phthalate (MiBP), which makes up 70% of the excretion products.

MiBP can be oxidized to either 2OH-mono-isobutyl phthalate (2OH-MiBP) or 3OH-mono-isobutyl phthalate (3OH-MiBP), which make up 20% and 1% of the excretion products respectively.
These reactions are likely catalyzed by cytochrome P450 in the liver.

The ratio between MiBP and the oxidized metabolites changes depending on the amount of time that has passed since exposure.
The ratio between MiBP and 2OH-MiBP and that between MiBP and 3OH-MiBP show a similar trend.
With the ratios being high, around 20-30:1, shortly after exposure and dropping gradually as more time passes to rest around 2-5:1.

Therefore, a high ratio of oxidized metabolites to the monoester metabolite suggests that there was recent exposure to Palatinol IC, within a few hours of measuring, while a lower ratio suggests that there has been more time since exposure.
In addition to oxidation, MiBP can also undergo a glucuronidation reaction, resulting in the metabolite MiBP-glucuronide

History of Palatinol IC:
In 1836 French chemist Auguste Laurent oxidized naphthalene with chromic acid and created phthalic anhydride, of which phthalates are derived.
Phthalates, including Palatinol IC, were first introduced in the 1920s to make plastics more flexible, transparent and long-lived.

They increased their popularity in 1931 when polyvinylchloride (PVC) became commercially available.
Due to the increase in human exposure to phthalates, in 1999 the European Union restricted the use of some of them in children’s toys

Storage of Palatinol IC:
Palatinol IC should be stored in a cool, dry, and well-ventilated place.
Palatinol IC should be stored in a Metal drum, stainless steel, aluminum, or polyester-reinforced resin.

Palatinol IC should be kept away from food.
Palatinol IC should be stored in containers, separately from Strong oxidants.

Handling and Storage of Palatinol IC:

Precautions for safe handling:

Advice on safe handling:
Work under hood.

Hygiene measures:
Immediately change contaminated clothing.
Apply preventive skin protection.
Wash hands and face after working with Palatinol IC.

Conditions for safe storage, including any incompatibilities:

Storage conditions:
Tightly closed.
Keep in a well-ventilated place.
Keep locked up or in an area accessible only to qualified or authorized persons.

Stability and Reactivity of Palatinol IC:

Reactivity:
Palatinol IC reacts with acids to liberate heat along with isobutyl alcohol and phthalic acid.
Palatinol IC may react sufficiently exothermically with strong oxidizing acids to ignite the reaction products.

Heat is also generated by interaction with caustic solutions.
Flammable hydrogen is generated by mixing with alkali metals and hydrides.
Palatinol IC can generate electrostatic charges in handling

Chemical stability:
Palatinol IC is chemically stable under standard ambient conditions (room temperature).

Possibility of hazardous reactions:
No data available

First Aid Measures of Palatinol IC:

General advice:
Show Palatinol IC safety data sheet to the doctor in attendance.

If inhaled:

After inhalation:
Fresh air.
Call in physician.

In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Consult a physician.

In case of eye contact:

After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.

If swallowed:

After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.

Indication of any immediate medical attention and special treatment needed
No data available

Fire Fighting Measures of Palatinol IC:

Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder

Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.

Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.

Accidental Release Measures of Palatinol IC:

Environmental precautions:
Do not let product enter drains.

Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.

Observe possible material restrictions.
Take up carefully with liquid-absorbent material.

Dispose of properly.
Clean up affected area.

Identifiers of Palatinol IC:
CAS Number: 84-69-5
Molecular Weight: 278.34
Beilstein: 2054802
EC Number: 201-553-2
MDL number: MFCD00026480
Chemical formula: C16H22O4
Molar mass: 278.348 g·mol−1
Appearance: Colorless viscous liquid
Density: 1.038 g/cm3
Melting point: −37 °C (−35 °F; 236 K)
Boiling point: 320 °C (608 °F; 593 K)
Solubility in water: 1 mg/L at 20 °C
log P: 4.11
Vapor pressure: 0.01 Pa at 20 °C
Flash point: 185 °C (365 °F; 458 K) c.c.
Autoignition temperature: 400 °C (752 °F; 673 K)

Melting Point: -37 °C
Flammability: Combustible
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 296.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.002000 mmHg @ 25.00 °C. (est)
Flash Point: 309.00 °F. TCC (153.90 °C.) (est)
logP (o/w): 4.110
Soluble in: water, 6.2 mg/L @ 24C (exp)
CAS: 84-74-2
EINECS: 201-557-4
InChIKey: DOIRQSBPFJWKBE-UHFFFAOYSA-N
Molecular Formula: C16H22O4
Molar Mass: 278.34

Storage Condition: 2-8°C
Sensitive: Easily absorbing moisture
Explosive Limit: 0.47%, 236°F
Refractive Index: n20/D 1.492(lit.)
MDL: MFCD00009441
Chemical Formula: C16H22O4
Average Molecular Mass: 278.344 g/mol
Monoisotopic Mass: 278.152 g/mol
CAS Registry Number: 84-69-5
IUPAC Name: 1,2-bis(2-methylpropyl) benzene-1,2-dicarboxylate
Traditional Name: Palatinol IC
SMILES: CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C
InChI Identifier: InChI=1S/C16H22O4/c1-11(2)9-19-15(17)13-7-5-6-8-14(13)16(18)20-10-12(3)4/h5-8,11-12H,9-10H2,1-4H3
InChI Key: InChIKey=MGWAVDBGNNKXQV-UHFFFAOYSA-N

Properties of Palatinol IC:
Molecular Weight: 278.34 g/mol
XLogP3: 4.1
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 8
Exact Mass: 278.15180918 g/mol
Monoisotopic Mass: 278.15180918 g/mol
Topological Polar Surface Area: 52.6Ų
Heavy Atom Count: 20
Complexity: 290
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Physical state: liquid
Color: colorless
Odor: weak
Melting point/freezing point:
Melting point: -64 °C
Initial boiling point and boiling range: 327 °C - lit.
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits:
Upper explosion limit: 3,2 %(V)
Lower explosion limit: 0,8 %(V)
Flash point: 109 °C - closed cup
Autoignition temperature: 423 °C at 1.013 hPa
Decomposition temperature: No data available
pH: neutral

Viscosity:
Viscosity, kinematic: 13,96 mm2/s at 40 °C
Viscosity, dynamic: No data available
Water solubility 0,02 g/l at 20 °C - slightly soluble
Partition coefficient: n-octanol/water:
log Pow: 4,11 at 20 °C
Vapor pressure: 0,11 hPa at 100 °C
Density: 1,039 g/cm3 at 25 °C - lit.
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: none
Other safety information: No data available

Melting Point: -64 °C
Boiling Point: 295.3±8.0 °C at 760 mmHg
Flash Point: 153.9±7.9 °C
Molecular Formula: C16H22O4
Molecular Weight: 278.344
Density: 1.0±0.1 g/cm3
Molecular Formula: C16H22O4
IUPAC name: bis(2-methylpropyl) benzene-1,2-dicarboxylate
Cas Number: 84-69-5
Molecular weight: 278.34 g/mol
Density: 1.039 g/mL
Boiling Point: 320 °C
Flashpoint: 185 °C

Density: 1.043 g/mL at 25 °C (lit.)
Melting Point: -35 °C (lit.)
Boling Point: 340 °C (lit.)
Flash Point: 340°F
Water Solubility: Slightly soluble. 0.0013 g/100 mL
Solubility: Soluble in water (0.4 mg/ml at 20 °C), ethanol.
Very soluble in ether, acetone, and B
Vapor Presure: 1 mm Hg ( 147 °C)
Vapor Density: 9.6 (vs air)
Appearance: Colorless liquid
Specific Gravity: 1.049 (20/20℃)
Color: APHA: ≤10
Exposure Limit NIOSH REL: TWA 5 mg/m3, IDLH 4,000 mg/m3;
OSHA PEL: TWA5 mg/m3; ACGIH TLV: TWA 5 mg/m3.
Merck: 14,3035
BRN: 1914064

Compound Type of Palatinol IC:
Aromatic Hydrocarbon
Cosmetic Toxin
Ester
Ether
Household Toxin
Industrial/Workplace Toxin
Metabolite
Organic Compound
Phthalate
Plasticizer
Synthetic Compound

Alternative Parents of Palatinol IC:
Benzoyl derivatives
Dicarboxylic acids and derivatives
Carboxylic acid esters
Organooxygen compounds
Organic oxides
Hydrocarbon derivatives

Substituents of Palatinol IC:
Benzoate ester
Benzoyl
Dicarboxylic acid or derivatives
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aromatic homomonocyclic compound
PALMERA A 9912
Palmera A 9912 acts as a surfactant.
Palmera A 9912 is a main renewable ingredient for production of soaps.
Palmera A 9912 is a conjugate acid of a dodecanoate.


CAS Number: 143-07-7
EC Number: 205-582-1
MDL number: MFCD00002736
Chemical formula: C12H24O2
Linear Formula: CH3(CH2)10COOH


Palmera A 9912 is a naturally occurring fatty acid common in coconut oil.
Palmera A 9912's formula C12H24O2 responds to saturated monocarboxylic acid and corresponds to a straight chain carboxylic acid with 12 carbon atoms.
Palmera A 9912 acts as a surfactant.


Palmera A 9912 is a straight-chain saturated fatty acid and a medium-chain fatty acid.
Palmera A 9912 is a conjugate acid of a dodecanoate.
Palmera A 9912, also known as dodecanoate, belongs to the class of organic compounds known as medium-chain fatty acids.


Palmera A 9912 is a middle chain-free fatty acid with strong bactericidal properties.
Palmera A 9912 is obtained from fractionation of a lauric-type oil.
Palmera A 9912 obtained has a melting point above 43 º C.


Palmera A 9912 is solid at room temperature, opaque white and with a characteristic odour.
Palmera A 9912 and myristic acid are saturated fatty acids.
Palmera A 9912 is fatty acid derived from renewable vegetable oils.


Palmera A 9912 is one of several fatty acids found in coconut oil, babassu butter and other natural fats.
People also use Palmera A 9912 as medicine.
People use Palmera A 9912 for viral infections such as the flu, common cold, genital herpes, and many other conditions, but there is no good scientific evidence to support any use.


Palmera A 9912, also known as dodecanoate, belongs to the class of organic compounds known as medium-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.
Palmera A 9912 is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.


As a raw material, Palmera A 9912 can appear as a colorless solid or as a slightly glossy white or yellow crystalline solid or powder.
Palmera A 9912 is a fatty acid, esters of which occur in natural substances such as coconut milk and palm kernel oil.
Palmera A 9912 has a role as a plant metabolite, an antibacterial agent and an algal metabolite.


Palmera A 9912 increases total serum lipoproteins more than many other fatty acids, but mostly high-density lipoprotein (HDL).
Palmera A 9912 belongs to the class of organic compounds known as medium-chain fatty acids.
Palmera A 9912 may be animal- or plant-derived.


Palmera A 9912 is a middle chain-free fatty acid with strong bactericidal properties.
Palmera A 9912 derives from a hydride of a dodecane.
Palmera A 9912 is also called dodecanoic acid.


Palmera A 9912’s a medium chain triglyceride (MCT) also naturally present in skin’s oil.
This fatty acid, Palmera A 9912, plays an important role in reinforcing skin’s innate defenses by strengthening its microbiome.
Both are white solids that are very slightly soluble in water.


Palmera A 9912 esters (principally triglycerides) are found only in vegetable fats, primarily from coconut milk and oil, laurel oil, and palm kernel oil.
In contrast, myristic acid triglycerides occur in plants and animals, notably in nutmeg butter, coconut oil, and mammalian milk.
Palmera A 9912 is a medium-chain saturated fatty acid.


Palmera A 9912 is a precursor to dilauroyl peroxide, a common initiator of polymerizations.
Palmera A 9912 is found in many vegetable fats and in coconut and palm kernel oils.
Palmera A 9912 contains C12 (>99%) fatty acid.


Palmera A 9912’s a medium-length long-chain fatty acid, or lipid, that makes up about half of the fatty acids within coconut oil.
Palmera A 9912, myristic acid, and palmitic acid all increased LDL and HDL cholesterol concentrations as compared with carbohydrates.
Palmera A 9912, systematically dodecanoic acid, is a saturated fatty acid with a 12-carbon atom chain, thus having many properties of medium-chain fatty acids.


Both are white solids that are very slightly soluble in water.
Like many other fatty acids, Palmera A 9912 is inexpensive, has a long shelf-life, is nontoxic, and is safe to handle.
Palmera A 9912 is used mainly for the production of soaps and cosmetics.


In nature Palmera A 9912 is accompanied by other saturated fatty acids as caprylic acid, capric, myristic, palmitic and stearic.
Palmera A 9912 is non-toxic, safe to handle, inexpensive, and has a long shelf life.
Palmera A 9912 has multiple uses in cosmetics, including as an emulsifier and texture-enhancing ingredient.


Palmera A 9912, systematically dodecanoic acid, is a saturated fatty acid with a 12-carbon atom chain, thus having many properties of medium-chain fatty acids.
A 12 carbon length fatty acid that can be found naturally in coconut milk, coconut oil, laurel oil, and palm kernel oil.
Palmera A 9912's also in breast milk.


Palmera A 9912 is readily biodegradable and is GMO-free.
Palmera A 9912 belongs to the class of organic compounds known as medium-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.


Palmera A 9912 is one of those active parts.
Palmera A 9912, the chemical name of which is dodecanoic acid, is a medium chain fatty acid that is found in coconut oil.
Palmera A 9912 is a bright white, powdery solid with a faint odor of bay oil or soap.


Palmera A 9912 is a major component of coconut oil and palm kernel oil.
Palmera A 9912, C12H24O2, also known as dodecanoic acid, is a saturated fatty acid with a 12-carbon atom chain.
Palmera A 9912 is a bright white, powdery solid with a faint odor of bay oil or soap.


Palmera A 9912 is also called dodecanoic acid.
Palmera A 9912 is bovine spongiform encephalopathy/ transmissible spongiform encephalopathy-free.
Palmera A 9912 is a saturated fat.


Palmera A 9912 belongs to the group of saturated fatty acids since there is no double bond in the aliphatic chain, so its shorthand notation is 12:0.
Palmera A 9912 is found in many vegetable fats, particularly in coconut and palm kernel oils.
Palmera A 9912 is a saturated fatty acid, which is found in animal and plant fats and oils, and is a major component of coconut oil and palm kernel oil.


Otherwise, Palmera A 9912 is relatively uncommon.
Palmera A 9912 is also found in human breast milk (6.2% of total fat), cow's milk (2.9%), and goat's milk (3.1%).
Palmera A 9912, a saturated medium-chain fatty acid with a 12-carbon backbone, is naturally found in various plant and animal fats and oils, which is a major component of palm kernel oil and coconut oil.


Palmera A 9912 esters (principally triglycerides) are found only in vegetable fats, primarily from coconut milk and oil, laurel oil, and palm kernel oil.
Palmera A 9912 is a precursor to dilauroyl peroxide, a common initiator of polymerizations.
Palmera A 9912 is one of those active parts.


Palmera A 9912’s a medium-length long-chain fatty acid, or lipid, that makes up about half of the fatty acids within coconut oil.
The salts and esters of Palmera A 9912 are known as laurates.
Like many other fatty acids, Palmera A 9912 is inexpensive, has a long shelf-life, is nontoxic, and is safe to handle.


Palmera A 9912 is mostly derived from the hydrolysis of coconut oil or palm kernel oil, and its subsequent distillation (approx. 50% wealth).
Palmera A 9912 is a main renewable ingredient for production of soaps.
The salts and esters of Palmera A 9912 are known as laurates.


Palmera A 9912, as a component of triglycerides, comprises about half of the fatty-acid content in coconut milk, coconut oil, laurel oil, and palm kernel oil (not to be confused with palm oil).
For these purposes, Palmera A 9912 is reacted with sodium hydroxide to give sodium laurate, which is a soap.


Most commonly, sodium laurate is obtained by saponification of various oils, such as coconut oil.
These precursors give mixtures of sodium laurate and other soaps.
Palmera A 9912 is a biodegradable, GMO-free and fatty oil derived from renewable vegetable oil by KLK Oleo works as a surfactant, emollient and cleansing agent.


Palmera A 9912 is properly known as dodecanoic acid, is a saturated fatty acid commonly found in coconut and palm oils, as well as in milk.
Palmera A 9912, CAS 143-07-7, chemical formula C12H24O2, is produced as a white crystalline powder, has a slight odor of bay oil, and is soluble in water, alcohols, phenyls, haloalkanes, and acetates.


Palmera A 9912 and myristic acid are saturated fatty acids.
Palmera A 9912 is a member of the sub-group called medium chain fatty acids or MCFA, namely fatty acids containing from 6 to 12 carbon atoms.
Their formal names are dodecanoic acid and tetradecanoic acid, respectively.


Palmera A 9912 is the major fatty acid present in vegetable oils such as coconut oil in and palm kernel oil.
Palmera A 9912 is a straight-chain, twelve-carbon medium-chain saturated fatty acid with strong bactericidal properties; the main fatty acid in coconut oil and palm kernel oil.
Palmera A 9912 is Halal and Kosher certified.



USES and APPLICATIONS of PALMERA A 9912:
Palmera A 9912's applications include toiletries, transparent soaps and other cosmetic care products.
Palmera A 9912 is used in production of various esters, fatty alcohols, fatty acid isethionates, metallic soaps, fatty acid sarcosinates, imidazolines and fatty amines.

Palmera A 9912 is a versatile oleochemical with applications in everything from plastics to personal care.
Palmera A 9912 is a medium-chain saturated fatty acid.
Palmera A 9912 is found in many vegetable fats and in coconut and palm kernel oils.


Palmera A 9912 is an inexpensive, non-toxic and safe to handle compound often used in laboratory investigations of melting-point depression.
Palmera A 9912 is used mainly for the production of soaps and cosmetics.
For these purposes, Palmera A 9912 is reacted with sodium hydroxide to give sodium laurate, which is a soap.


Palmera A 9912 is suitable for soaps, toiletries, transparent soaps, and other cosmetic care products.
In addition, Palmera A 9912 is used in the production of various esters, fatty alcohols, fatty acid isethionates, metallic soaps, fatty acid sarcosinates, imidazolines, and fatty amines.


Palmera A 9912 is an emulsifying agent, also used as a cleaning agent or as a surfactant.
Palmera A 9912 is an inexpensive, non-toxic and safe to handle compound often used in laboratory investigations of melting-point depression.
Research continues to investigate Palmera A 9912’s benefits as an adjunct to anti-acne treatments.


Palmera A 9912 is used Pharma and healthcare, Lubricants, Paints and coatings, Industrial chemistry, Personal hygiene, and home care.
Palmera A 9912 is mainly used as a raw material for the production of alkyd resins, wetting agents, detergents, insecticides, surfactants, food additives and cosmetics.


Palmera A 9912 is often used as a lubricant and has multiple functions such as lubricant and vulcanizing agent.
However, due to its corrosive effect on metals, Palmera A 9912 is generally not used in plastic products such as wires and cables.
Palmera A 9912 is used in the medicine industry.


Palmera A 9912's natural bay leaf-like scent can be used in high amounts to add fragrance to products, but it’s more often used as a base for cleansing agents, and, increasingly, for its skin-soothing actions.
Palmera A 9912 is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.


Some studies have shown Palmera A 9912 can also have antimicrobial activity.
Palmera A 9912 is typically used in under 10% concentration in cosmetic formulas but has been deemed safe in higher concentrations (up to 25%).
Palmera A 9912 is also used for preventing the transmission of HIV from mothers to children.


Palmera A 9912 is widely used in cosmetics, latex and gloves.
Palmera A 9912 is used for treating viral infections including influenza (the flu); swine flu; avian flu; the common cold; fever blisters, cold sores, and genital herpes caused by herpes simplex virus (HSV); genital warts caused by human papillomavirus (HPV); and HIV/AIDS.


Palmera A 9912 is also used for preventing the transmission of HIV from mothers to children.
Palmera A 9912 is a solid at room temperature but melts easily in boiling water, so liquid Palmera A 9912 can be treated with various solutes and used to determine their molecular masses.


Palmera A 9912 is most widely used in the surfactant industry and can also be used in the perfume industry and pharmaceutical industry.
Palmera A 9912 is used as a surface treatment agent for the preparation of bonding.
Palmera A 9912 is also used in the manufacture of alkyd resins, chemical fiber oils, insecticides, synthetic fragrances, plastic stabilizers, anti-corrosion additives for gasoline and lubricating oils.


Palmera A 9912 is widely used in the manufacture of various types of surfactants, such as cationic laurylamine, trilaurylamine, lauryl dimethylamine, lauryl trimethylammonium salt, etc.; anionic types include sodium lauryl sulfate and lauric acid sulfuric acid Ester salts, triethanol ammonium lauryl sulfate, etc.; zwitterionic types include lauryl betaine, imidazoline laurate, etc.; non-ionic surfactants include poly-L-alcohol monolaurate, polyoxyethylene laurate , glyceryl laurate polyoxyethylene ether, lauric acid diethanolamide, etc.


In addition, Palmera A 9912 is also used as a food additive and in the manufacture of cosmetics.
Palmera A 9912 is the raw material for producing soap, detergent, cosmetic surfactant, and chemical fiber oil.


-Uses & Applications of Palmera A 9912:
*Plastics: Intermediate
*Food and Beverage: Raw Material for Emulsifiers
*Surfactants and Esters: Anionic and Nonionic Surfactants
*Textiles: Lubricant & Process Agent
*Personal Care: Emulsifier for Facial Creams and Lotions
*Soaps and Detergents: A Base in the Production of Liquid and Transparent Soaps


-Cosmetic Uses:
*cleansing agents
*surfactants
*surfactant - emulsifying



PALMERA A 9912 AT A GLANCE:
*Natural component of skin’s oil
*Plays a role in reinforcing skin’s innate defenses by strengthening its microbiome
*Functions as a cleansing agent/emulsifier in cosmetic formulas
*Studies have shown Palmera A 9912 offers antimicrobial activity
*Can be sourced from coconut oil, babassu butter and other natural fats



PROPERTIES OF PALMERA A 9912:
Palmera A 9912 enhances the antimicrobial protective properties of the skin, has an antibacterial effect, negatively affects a variety of pathogenic microorganisms, bacteria, yeast, fungi and viruses.



WHAT DOES PALMERA A 9912 DO IN A FORMULATION?
*Cleansing
*Emulsifying
*Surfactant



ALTERNATIVE PARENTS OF PALMERA A 9912:
*Straight chain fatty acids
*Monocarboxylic acids and derivatives
*Carboxylic acids
*Organic oxides
*Hydrocarbon derivatives
*Carbonyl compounds



RELATED COMPOUNDS OF PALMERA A 9912:
*Undecanoic acid
*Tridecanoic acid
*Dodecanol
*Dodecanal
*Sodium lauryl sulfate



SUBSTITUENTS OF PALMERA A 9912:
*Medium-chain fatty acid
*Straight chain fatty acid
*Monocarboxylic acid or derivatives
*Carboxylic acid
*Carboxylic acid derivative
*Organic oxygen compound
*Organic oxide
*Hydrocarbon derivative
*Organooxygen compound
*Carbonyl group
*Aliphatic acyclic compound



PALMERA A 9912 FOR PSORIASIS:
Bloggers and natural health websites often recommend coconut oil as a treatment for dry skin and conditions such as psoriasis.
Again, because Palmera A 9912 is only part of what makes up coconut oil, it’s difficult to say if the fatty acid alone or a combination of coconut oil components is responsible for these benefits.



PALMERA A 9912 FOR ACNE:
Because Palmera A 9912 has antibacterial properties, it’s been found to effectively combat acne.
The bacteria Propionibacterium acnes are found naturally on the skin.
When they overgrow, they lead to the development of acne.
The results of a 2009 study found that Palmera A 9912 could reduce inflammation and the number of bacteria present.

Palmera A 9912 worked even better than benzoyl peroxide, a common acne treatment.
A 2016 study also reconfirmed the acne-fighting properties of Palmera A 9912.
This doesn’t mean you should put coconut oil on your acne.
The researchers used pure Palmera A 9912 and suggested that it could be developed into an antibiotic therapy for acne in the future.



HOW TO USE PALMERA A 9912:
To reap the topical benefits of Palmera A 9912 and coconut oil, apply it directly to your skin.
While this isn’t recommended for people with acne, the risks are minimal when it comes to addressing issues such as skin hydration and psoriasis.
Coconut oil can be used in cooking as well.
Its sweet, nutty flavor makes Palmera A 9912 the perfect addition to desserts, including double chocolate paleo brownies and paleo banana bread.
You can also use Palmera A 9912 to sauté vegetables or to add flavor to mashed sweet potatoes or a Caribbean curry soup.



IN VARIOUS PLANTS, PALMERA A 9912:
The palm tree Attalea speciosa, a species popularly known in Brazil as babassu – 50% in babassu oil
Attalea cohune, the cohune palm (also rain tree, American oil palm, corozo palm or manaca palm) – 46.5% in cohune oil
Astrocaryum murumuru (Arecaceae) a palm native to the Amazon – 47.5% in "murumuru butter"
Coconut oil 49%

Pycnanthus kombo (African nutmeg)
Virola surinamensis (wild nutmeg) 7.8–11.5%
Peach palm seed 10.4%
Betel nut 9%

Date palm seed 0.56–5.4%
Macadamia nut 0.072–1.1%
Plum 0.35–0.38%
Watermelon seed 0.33%
Viburnum opulus 0.24-0.33%

Citrullus lanatus (egusi melon)
Pumpkin flower 205 ppm, pumpkin seed 472 ppm
In Insects
Black soldier fly Hermetia illucens 30–50 mg/100 mg fat.



WHERE TO FIND PALMERA A 9912:
Palmera A 9912 is a powerful substance that’s sometimes extracted from the coconut for use in developing monolaurin.
Monolaurin is an antimicrobial agent that’s able to fight pathogens such as bacteria, viruses, and yeasts.



NUTRITIONAL AND MEDICAL ASPECTS OF PALMERA A 9912:
Although 95% of medium-chain triglycerides are absorbed through the portal vein, only 25–30% of Palmera A 9912 is absorbed through it.
Palmera A 9912 increases total serum lipoproteins more than many other fatty acids, but mostly high-density lipoprotein (HDL).
As a result, Palmera A 9912 has been characterized as having "a more favorable effect on total HDL than any other fatty acid [examined], either saturated or unsaturated".

In general, a lower total/HDL serum lipoprotein ratio correlates with a decrease in atherosclerotic incidence.
Nonetheless, an extensive meta-analysis on foods affecting the total LDL/serum lipoprotein ratio found in 2003 that the net effects of Palmera A 9912 on coronary artery disease outcomes remained uncertain.
A 2016 review of coconut oil (which is nearly half Palmera A 9912) was similarly inconclusive about the effects on cardiovascular disease incidence



PHYSICAL and CHEMICAL PROPERTIES of PALMERA A 9912:
Chemical formula: C12H24O2
Molar mass: 200.322 g·mol−1
Appearance: White powder
Odor: Slight odor of bay oil
Density: 1.007 g/cm3 (24 °C)
0.8744 g/cm3 (41.5 °C)
0.8679 g/cm3 (50 °C)
Melting point: 43.8 °C (110.8 °F; 316.9 K)
Boiling point: 297.9 °C (568.2 °F; 571.0 K)
282.5 °C (540.5 °F; 555.6 K) at 512 mmHg
225.1 °C (437.2 °F; 498.2 K) at 100 mmHg
Solubility in water: 37 mg/L (0 °C)
55 mg/L (20 °C), 63 mg/L (30 °C)
72 mg/L (45 °C), 83 mg/L (100 °C)

Solubility: Soluble in alcohols, diethyl ether, phenyls, haloalkanes, acetates
Solubility in methanol: 12.7 g/100 g (0 °C)
120 g/100 g (20 °C), 2250 g/100 g (40 °C)
Solubility in acetone: 8.95 g/100 g (0 °C)
60.5 g/100 g (20 °C), 1590 g/100 g (40 °C)
Solubility in ethyl acetate: 9.4 g/100 g (0 °C)
52 g/100 g (20°C), 1250 g/100 g (40°C)
Solubility in toluene: 15.3 g/100 g (0 °C)
97 g/100 g (20°C), 1410 g/100 g (40°C)
log P: 4.6
Vapor pressure: 2.13·10−6 kPa (25 °C)
0.42 kPa (150 °C), 6.67 kPa (210 °C)
Acidity (pKa): 5.3 (20 °C)
Thermal conductivity: 0.442 W/m·K (solid)
0.1921 W/m·K (72.5 °C)
0.1748 W/m·K (106 °C)
Refractive index (nD): 1.423 (70 °C), 1.4183 (82 °C)

Viscosity: 6.88 cP (50 °C), 5.37 cP (60 °C)
Structure
Crystal structure: Monoclinic (α-form)
Triclinic, aP228 (γ-form)
Space group: P21/a, No. 14 (α-form)
P1, No. 2 (γ-form)
Point group: 2/m (α-form), 1 (γ-form)
Lattice constant:
a = 9.524 Å, b = 4.965 Å, c = 35.39 Å (α-form)
α = 90°, β = 129.22°, γ = 90°
Thermochemistry
Heat capacity (C): 404.28 J/mol·K
Std enthalpy of formation (ΔfH⦵298): −775.6 kJ/mol
Std enthalpy of combustion (ΔcH⦵298): 7377 kJ/mol, 7425.8 kJ/mol (292 K)
CAS number: 143-07-7
EC number: 205-582-1
Hill Formula: C₁₂H₂₄O₂

Chemical formula: CH₃(CH₂)₁₀COOH
Molar Mass: 200.32 g/mol
HS Code: 2915 90 30
Water Solubility: 0.01 g/L
logP: 5.13
logP: 4.48
logS: -4.3
pKa (Strongest Acidic): 4.95
Physiological Charge: -1
Hydrogen Acceptor Count: 2
Hydrogen Donor Count: 1
Polar Surface Area: 37.3 Ų
Rotatable Bond Count: 10
Refractivity: 58.68 m³·mol⁻¹
Polarizability: 25.85 ų
Number of Rings: 0
Bioavailability: 1
Rule of Five: Yes
Ghose Filter: Yes
Veber's Rule: Yes
MDDR-like Rule: Yes

Boiling point: 299 °C (1013 hPa)
Density: 0.883 g/cm3 (50 °C)
Explosion limit: 0.6 %(V)
Flash point: 176 °C
Ignition temperature: 250 °C
Melting Point: 43 - 45 °C
Vapor pressure: Bulk density: 490 kg/m3
Solubility: 4.81 mg/l
Physical state: solid
Color: white, to, light yellow
Odor: weak characteristic odour
Melting point/freezing point:
Melting point: 43 - 45 °C
Initial boiling point and boiling range: 299 °C at 1.013 hPa
Flammability (solid, gas): The product is not flammable.
Upper/lower flammability or explosive limits:

Lower explosion limit: 0,6 %(V)
Flash point: 176 °C - closed cup
Autoignition temperature: > 250 °C
Decomposition temperature: No data available
pH: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: 7 mPa.s at 50 °C
Water solubility: 0,058 g/l at 20 °C
Partition coefficient: n-octanol/water:
log Pow: 4,6 - (Lit.), Potential bioaccumulation
Vapor pressure 0,15 hPa at 100 °C < 0,1 hPa at 25 °C - (Lit.)
Density: 0,883 g/cm3 at 50 °C
Relative density No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available

Oxidizing properties: none
Other safety information:
Bulk density: ca.490 kg/m3
Surface tension: 26,6 mN/m at 70 °C
Dissociation constant: 5,3 at 20 °C
Relative vapor density: 6,91
Molecular Weight: 278.43
Molecular Formula: C18H30O2
Boiling Point: 230-232ºC1 mm Hg(lit.)
Melting Point: -11ºC(lit.)
Flash Point: >230 °F
Purity: 95%
Density: 0.914 g/mL at 25 °C(lit.)
Storage: 2-8ºC
Assay: 0.99
Refractive Index: n20/D 1.480(lit.)

Appearance: white to pale yellow waxy crystalline solid (est)
Assay: 95.00 to 100.00 sum of isomers
Water Content: <0.20%
Food Chemicals Codex Listed: Yes
Melting Point: 45.00 to 48.00 °C. @ 760.00 mm Hg
Boiling Point: 225.00 °C. @ 100.00 mm Hg
Boiling Point: 252.00 to 287.00 °C. @ 760.00 mm Hg
Congealing Point: 26.00 to 44.00 °C.
Saponification Value: 253.00 to 287.00
Unsaponifiable Matter: <0.30%
Vapor Pressure: 0.001000 mmHg @ 25.00 °C. (est)
Vapor Density: 6.91 ( Air = 1 )
Flash Point: 329.00 °F. TCC ( 165.00 °C. )
logP (o/w): 4.600
Soluble in: alcohol, chloroform, ether
water, 12.76 mg/L @ 25 °C (est)
water, 4.81 mg/L @ 25 °C (exp)



FIRST AID MEASURES of PALMERA A 9912:
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Immediately call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of PALMERA A 9912:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of PALMERA A 9912:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of PALMERA A 9912:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
protective clothing
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of PALMERA A 9912:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
*Storage class:
Storage class (TRGS 510): 13:
Non Combustible Solids



STABILITY and REACTIVITY of PALMERA A 9912:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .



SYNONYMS:
Dodecanoic acid
n-Dodecanoic acid
Dodecylic acid
Dodecoic acid
Laurostearic acid
Vulvic acid
1-Undecanecarboxylic acid
Duodecylic acid, C12:0 (Lipid numbers)
Dodecanoic acid, ABL, Lauric acid
C18:3 (ALL CIS-9,12,15) ACID
CIS,CIS,CIS-9,12,15-OCTADECATRIENOIC ACID
DELTA 9 CIS 12 CIS 15 CIS OCTADECATRIENOIC ACID
9,12,15-OCTADECATRIENIC ACID
9,12,15-OCTADECATRIENOIC ACID
ALFA-LINOLENIC ACID
ALL CIS-9,12,15-OCTADECATRIENOIC ACID
ALPHA-LINOLENIC AC
1-Undecanecarboxylate
1-Undecanecarboxylic acid
ABL
Acide Laurique
C12 fatty acid
C12:0
Coconut oil fatty acids
DAO
Dodecanoate
dodecanoic acid
dodecoate
Dodecoic acid
Dodecylate
dodecylcarboxylate
Dodecylic acid
duodecyclate
Duodecyclic acid
duodecylate
Duodecylic acid
LAP
LAU
Laurate
Lauric acid
Laurinsaeure
Laurostearate
Laurostearic acid
MYR
n-Dodecanoate
n-Dodecanoic acid
Sorbitan laurate
Sorbitan monolaurate (NF)
undecane-1-carboxylate
Undecane-1-carboxylic acid
Vulvate
Vulvic acid
CH3-[CH2]10-COOH
Dodecylcarboxylic acid
Laate
Laic acid
Aliphat no. 4
Edenor C 1298-100
Emery 651
Hystrene 9512
Kortacid 1299
Lunac L 70
Lunac L 98
Neo-fat 12
Neo-fat 12-43
Nissan naa 122
Philacid 1200
Prifac 2920
Univol u 314
1-Dodecanoic acid
FA(12:0)




PALMERA B1220€
PALMERA B1220(E) Topped Palm Kernel Fatty Acid. PALMERA B1220(E) by KLK Emmerich GmbH acts as a surfactant. It is derived from renewable vegetable oils and fats. PALMERA B1220(E) is used in transparent soaps, toiletries, liquid soaps and other cosmetic care products. It is HACCP and GMP certified. Claims Surfactants / Cleansing Agents bio/ organic vegetal origin CAS Number 90990-15-1 Product Status COMMERCIAL PALMERA B1220(E) by KLK OLEO is a biodegradable, topped palm kernel fatty acid grade. Acts as a plasticizer. It is derived from renewable vegetable oils. PALMERA B1220(E) is free from genetically modified organisms (GMOs) and bovine spongiform encephalopathy/ transmissible spongiform encephalopathy (BSE/ TSE). Used in adhesive applications. Complies with USP-NF and KOSHER. It is HALAL, HACCP and GMP certified compound. Product Type Plasticizers > Fatty Acids Chemical Composition Topped palm kernel fatty acid Product Status COMMERCIAL PALMERA B1220(E) Fatty Acids PALMERA B1220(E) distilled and fractionated fatty acids are produced in accordance with the required demands and quality standards such as GMP and HACCP – making them suitable for food, pharmaceutical and personal care applications. It can be used as-is, or as a derivative. Fatty acids may be found in plastics, rubber, textiles, lubricants, metal-working, crayons, candles, biocides, paints, inks and etc. Fractionated Fatty Acids Caproic Acid Product Name: A9806, A9906 Application Fatty Acid Palmera B1220(E) Product description The portfolio of oleochemicals contains fractionated or distilled natural fatty acids, which are produced in accordance with GMP and HACCP quality regulations. Fatty acids build a base for various applications. The range contains different qualities such as cosmetic, pharmaceutical, food or technical compliant grades. A kosher and halal compliance can be ensured for the most products. Possible applications are: personal care and detergents, lubricants, plastics and rubber, textiles auxiliaries, candles, paints and varnishes, print colors and metalworking. Biesterfeld is member of the RSPO. Please contact us regarding certifications like Mass Balance (MB). More products available upon request. Tradename Chemical Description CAS Packaging Palmera B1220(E) Caprylic Acid 124-07-2 Drums Palmera B1220(E) Capric Acid 334-48-5 Drums Palmera B1220(E) Lauric Acid 143-07-7 Bags Palmera B1220(E) Myristic Acid 544-63-8 Bags Palmera B1220(E) Palmitic Acid 57-11-4 Bags Palmera B1220(E) Stearic Acid 57-11-4 Bags Palmera B1220(E) Oleic Acid 112-80-1 Drums Palmera B1220(E) Oleic Acid 112-80-1 Drums Palmera B1220(E) Erucic Acid 112-86-7 Drums Palmera B1220(E) Behenic Acid 112-85-6 Bags Palmera B1220(E) Tripple Pressed Stearic Acid 67701-03-5 Bags Palmera B1220(E) Stearic Acid 67701-03-5 Bags Palmera B1220(E) Stearic Acid (Long Chain) 68424-37-3 Bags Palmera B1220(E) Topped Palm Kernel Fatty Acid 67701-05-7 Drums Palmera B1220(E) Distilled Coconut Fatty Acid 67701-05-7 Drums Palmera B1220(E) Distilled Coconut Fatty Acid 67701-05-7 Drums Palmera B1220(E) Distilled Coconut Fatty Acid 67701-05-7 Drums The fatty acid stocks used in amidation reactions of the present invention may be coconut fatty acids, palm oil fatty acids, palm kernel fatty acids or combinations thereof among others. The fatty acid stock may be in treated form or not. Treated herein means distilled, hydrogenated, cut, uncut or combinations thereof. The fatty acid stocks used in present invention are commercial products of KLK OLEO company under the brand name of Palmera B1220(E). Palmera B1220(E) distilled coconut fatty acid. Carbon distribution by weight % is 5.33 C8, 6.38 C10, 51.13 C12, 17.66 C14, 7.43 C16, 1.74 C18, 7.63 C18:1, 1.1 C18:2. ** Palmera B1220(E) topped palm kernel fatty acid. Carbon distribution by weight % is 0.71 C10, 52.26 C12, 17.32 C14, 9.36 C16, 2.34 C18, 15.40 C18:1, 2.25 C18:2. *** as defined in "Analysis Methods" section. **** The betaine solution was not considered as flowable since gelation occurred. Thus, the related analysis was not done. determined Analysis: Water content (% wt.) 56.4 56.02 was not determined 55.53 59.33 was not determined Analysis: Viscosity (cP) 125 175 was not determined 25 75 was not determined Analysis: pH 5.74 5.63 was not determined 6.23 6.42 was not determined * Palmera B1220(E) distilled coconut fatty acid. Carbon distribution by weight % is 5.33 C8, 6.38 C10, 51.13 C12, 17.66 C14, 7.43 C16, 1.74 C18, 7.63 C18:1, 1.1 C18:2. ** Palmera B1220(E) topped palm kernel fatty acid. Carbon distribution by weight % is 0.71 C10, 52.26 C12, 17.32 C14, 9.36 C16, 2.34 C18, 15.40 C18:1, 2.25 C18:2. 6.95 was not determined was not determined 5.62 was not determined was not determined Analysis: Water content (% wt.) 52.52 was not determined was not determined 59.86 was not determined was not determined Analysis: Viscosity (cP) 300 was not determined was not determined 75 was not determined was not determined Analysis: pH 5.79 was not determined was not determined 6.6 was not determined was not determined * Palmera B1220(E) distilled coconut fatty acid. Carbon distribution by weight % is 5.33 C8, 6.38 C10, 51.13 C12, 17.66 C14, 7.43 C16, 1.74 C18, 7.63 C18:1, 1.1 C18:2. ** Palmera B1220(E) topped palm kernel fatty acid. Carbon distribution by weight % is 0.71 C10, 52.26 C12, 17.32 C14, 9.36 C16, 2.34 C18, 15.40 C18:1, 2.25 C18:2. *** as defined in "Analysis Methods" section. **** The betaine solution was not considered as flowable since gelation occurred. Thus, the related analysis was not done. [0078] * Palmera B1220(E) distilled coconut fatty acid. Carbon distribution by weight % is 5.33 C8, 6.38 C10, 51.13 C12, 17.66 C14, 7.43 C16, 1.74 C18, 7.63 C18:1, 1.1 C18:2. ** Palmera B1220(E) topped palm kernel fatty acid. Carbon distribution by weight % is 0.71 C10, 52.26 C12, 17.32 C14, 9.36 C16, 2.34 C18, 15.40 C18:1, 2.25 C18:2 . *** AA=amidoamine **** as defined in "Analysis Methods" section. ***** The betaine solution was not considered as flowable since gelation occurred. Thus, the related analysis was not done. EXAMPLE SET 5: PILOT SCALE ADDITIVE-FREE BETAINE PRODUCTION TRIALS 35.38 34.14 Betaine content (% wt.) Analysis: 6.63 6.56 Sodium chloride (% wt.) Analysis: 53.43 54.53 Water content (% wt.) Analysis: 112.5 87.5 Viscosity (cP) Analysis: 6.62 7.40 pH Freezing point <-6°C 10°C Gel point <-6°C 14°C Cloud point <-6°C 15°C * Palmera B1220(E) distilled coconut fatty acid. Carbon distribution by weight % is 6.80 C8, 7.84 C10, 51.44 C12, 17.11 C14, 6.89 C16, 1.09 C18, 7.60 C18:1, 1.24 C18:2. ** Palmera B1220(E) distilled hydrogenated coconut fatty acid. Carbon distribution by weight % is 5.61 C8, 8.59 C10, 49.54 C12, 17.75 C14, 8.28 C16, 8.41 C18. *** as defined in "Analysis Methods" section. PALMERA B1220(E) Caprylic-Capric Acid Blend 353-367 355-369 0.5 MAX 6 MAX 60 3.0Y 0.3R 0,7 0.5 MAX 53-63 35-45 1.5 MAX 180Kg PALMERA B1220(E) Caprylic Acid 98% 383-390 384-391 0.5 MAX 15-17 60 3.0Y 0.3R 0,7 0.5 MAX 98 MIN 2.0 MAX 180Kg PALMERA B1220(E) Caprylic Acid 99% 383-390 384-391 0.5 MAX 15-17 60 3.0Y 0.3R 0,7 1.0 MAX 99 MIN 1.0 MAX 180Kg PALMERA B1220(E) Capric Acid 98% 322-328 323-329 0.5 MAX 30-32 60 3.0Y 0.3R 0,5 2.0 MAX 98 MIN 2.0 MAX 180Kg PALMERA B1220(E) Capric Acid 99% 323-330 324-331 0.5 MAX 30-32 60 3.0Y 0.3R 0,5 1.0 MAX 99 MIN 1.0 MAX 180 Kg PALMERA B1220(E) Lauric Acid 70% 265-275 266-276 0.5 MAX 32-36 50 2.0Y 0.2R 1.0 MAX 70-77 22-29 2.0 MAX 25 Kg PALMERA B1220(E) Lauric Acid 98% 278-282 279-283 0.3 MAX 42-44 50 1.5Y 0.2R 0,5 2.0 MAX 98 MIN 2.0 MAX 25 Kg PALMERA B1220(E) Lauric Acid 99% 278-282 279-283 0.3 MAX 42-44 40 1.2Y 0.2R 0,5 1.0 MAX 99 MIN 1.0 MAX 25 Kg PALMERA B1220(E) Myristic Acid 98% 243-248 244-249 0.3 MAX 52-54 40 1.5Y 0.2R 0,5 2.0 MAX 98 MIN 2.0 MAX 25 Kg PALMERA B1220(E) Myristic Acid 99% 243-247 244-248 0.3 MAX 52-54 40 1.2Y 0.2R 0,5 1.0 MAX 99 MIN 1.0 MAX 25 Kg PALMERA B1220(E) Palmitic Acid 60% 209-215 210-216 0.5 MAX 53-57 50 2.0Y 0.2R 0,5 60-66 34-40 1.0 MAX 25 Kg PALMERA B1220(E) Palmitic Acid 80% 215-230 216-231 12 MAX 55 MIN 15.0Y 1.5R 2,5 98 MIN TRACE 80 MIN 20 MAX 25 Kg PALMERA B1220(E) Palmitic Acid 92% 216-220 217-221 0.5 MAX 58-62 40 2.0Y 0.2R 0,5 2.0 MAX 92-96 8.0 MAX 25 Kg PALMERA B1220(E) Palmitic Acid 95% 215-221 216-222 0.5 MAX 59-62 40 2.0Y 0.2R 0,5 94-98 5.0 MAX 25 Kg PALMERA B1220(E) Palmitic Acid 98% 216-220 217-221 0.3 MAX 60-63 40 2.0Y 0.2R 0,5 2.0 MAX 98 MIN 2.0 MAX 25 Kg PALMERA B1220(E) Stearic Acid 55% 204-210 205-211 0.7 MAX 55.5-57.5 60 3.0Y 0.3R 41-47 52-58 1.0 MAX 25 Kg PALMERA B1220(E) Stearic Acid 65% 200-206 201-207 0.8 MAX 58-61 60 3.0Y 0.3R 30-36 63-68 1.0 MAX 25 Kg PALMERA B1220(E) Stearic Acid 70% 199-205 200-206 0.8 MAX 58-62 60 3.0Y 0.3R 27-32 67-72 1.0 MAX 25 Kg PALMERA B1220(E) Stearic Acid 92% 194-201 195-202 1.0 MAX 66-69 100 3.0Y 0.5R 8.0 MAX 92-96 1.5 MAX 25 Kg PALMERA B1220(E) Oleic Acid 195-203 196-204 86 MIN 8.5 MAX 225 75 MIN 13 MAX 180 Kg PALMERA B1220(E) Oleic Acid 195-203 196-204 90-100 7.5 MAX 200 12.0Y 1.5R 70 MIN 18 MAX 180 Kg PALMERA B1220(E) Oleic Acid 195-203 196-204 90-100 8.0 MAX 200 12.0Y 1.5R PALMERA B1220(E) Triple Pressed Stearic Acid 207-213 208-214 0.5 MAX 54-57 50 2.0Y 0.2R 60-66 32-39 1.0 MAX 25 Kg PALMERA B1220(E) Triple Pressed Stearic Acid 206-212 207-213 0.5 MAX 54-57 50 2.0Y 0.2R 55-60 39-45 1.0 MAX 25 Kg PALMERA B1220(E) Triple Pressed Stearic Acid 205-211 206-212 0.5 MAX 54-57 50 2.0Y 0.2R 48-55 45-51 1.0 MAX 25 Kg PALMERA B1220(E) Double Pressed Stearic Acid 206-215 207-216 4.0 MAX 52-57 10.0Y 1.0R 25 Kg PALMERA B1220(E) Rubber Grade Stearic Acid 195 MIN 196 MIN 8 MAX 52 MIN 20.0Y 2.0R 25 Kg PALMERA B1220(E) Distilled Palm Stearine Fatty Acid 207-214 208-215 28-39 47-53 100 3.0Y 0.5R 0.5 MAX 2.0 MAX 56-65 4-7 24-33 4-8 0.5 MAX 180 Kg PALMERA B1220(E) Distilled Standard Palm Oil Fatty Acid 205-211 206-212 41-52 44-50 100 3.0Y 0.5R 44-53 3-8 31-41 6-11 0.5 MAX 180 Kg PALMERA B1220(E) Distilled Palm Oil Fatty Acid 204-210 205-211 46-56 42-48 100 3.0Y 0.5R 0.5 MAX 4.0 MAX 40-48 3-9 35-44 7-12 0.5 MAX 180 Kg PALMERA B1220(E) Distilled Palm Kernel Fatty Acid 248-262 249-263 15-20 22-27 100 5.0Y 0.5R 1-4 1-4 46-52 13-18 7-14 1-4 12-19 1-3 0.5 MAX 180 Kg PALMERA B1220(E) Topped Palm Kernel Fatty Acid 246-254 247-255 16-22 25-29 100 3.0Y 0.5R 1.0 MAX 46-52 15-20 8-15 1-5 12-20 4.0 MAX 0.5 MAX 180 Kg PALMERA B1220(E) Coconut Fatty Acid 261-275 262-276 7-12 22-26 125 5.0Y 0.7R 0.5 MAX 4-8 5-10 46-53 15-21 5-13 4.0 MAX 5-12 3.0 MAX 180 Kg PALMERA B1220(E) Low IV Topped Coconut Fatty Acid 250-260 251-261 1.0 MAX 28-32 60 2.0Y 0.3R 1.0 MAX 50-56 18-25 8-13 8-15 1.0 MAX 180 Kg PALMERA B1220(E) Low IV Topped Palm Kernel Fatty Acid 246-256 247-257 1.0 MAX 30-35 60 PALMERA B1220(E) Caproic Acid 99% 476-484 478-486 max. 0.5 max. 1.5 max. 0.3 min. 99.5 PALMERA B1220(E) Caprylic Acid 99% 383-390 384-391 max. 0.5 15-17 max. 3.0 max. 0.3 max. 60 max. 1.0 min. 99 max. 1.0 PALMERA B1220(E) Caprylic-Capric Acid Blend 353-367 355-369 max. 0.5 max. 6.0 max. 3.0 max. 0.3 max. 60 max. 0.5 53-63 35-45 max. 1.5 PALMERA B1220(E) Capric Acid 99% 323-330 324-331 max. 0.5 30-32 max. 3.0 max. 0.3 max. 60 max. 1.0 min. 99 max. 1.0 PALMERA B1220(E) Lauric Acid 70% 265-275 266-276 max. 0.5 32-36 max. 2.0 max. 0.2 max. 50 max. 1.0 70-77 22-29 max. 2.0 PALMERA B1220(E) Lauric Acid 88% 280-300 max. 0.5 37-41 max. 3 max. 0.5 5-8 4-6 86-89 max. 0.5 PALMERA B1220(E) Lauric Acid 92 - 94% 277-282 278-283 max. 0.5 40.0-44.0 max. 1.3 max. 0.3 max. 3.0 min. 92.0 max. 6.0 max. 2.0 PALMERA B1220(E) Lauric Acid 95% 280-290 max. 0.5 40-44 max. 1.5 max. 0.3 2.0-3.0 1.5-2.5 94.5-96.5 PALMERA B1220(E) Lauric Acid 99 - 100% 278-282 279-283 max. 0.3 42-44 max. 1.2 max. 0.2 max. 40 max. 1.0 min. 99.0 max. 1.0 PALMERA B1220(E) Myristic Acid 99% 243-247 244-248 max. 0.3 52-54 max. 1.2 max. 0.2 max. 40 max. 1.0 min. 99 max. 1.0 PALMERA B1220(E) Palmitic Acid 92% 216-220 217-221 max. 0.5 58-62 max. 2.0 max. 0.2 max. 40 max. 2.0 92-96 max. 8.0 PALMERA B1220(E) Palmitic Acid 98 - 100% 216-220 217-221 max. 1 61.0-63.0 max. 2.0 max. 0.4 ← max. 0.5 max. 0.9 min. 98.0 max. 1.7 PALMERA B1220(E) Fractionated Coconut Fatty Acid 275-286 max. 3 max. 10.0 max. 1.5 4.0-12.0 6.0-12.0 57-67 23-30 Fractionated Fatty Acids Short Chains Fatty Acids Fatty Acids PALMERA B1220(E) distilled and fractionated fatty acids are derived from vegetable oils and fats. They can be used as-is, or as a derivative. Fatty acids may be found in plastics, rubber, textiles, lubricants, metal-working, crayons, candles, biocides, PALMERA B1220(E) Stearic Acid 70% 199-205 200-206 max. 0.8 58-62 max. 3.0 max. 0.3 60 27-32 67-72 max. 1.0 PALMERA B1220(E) Stearic Acid 90% 195-199 196-200 max. 1 66-69 max. 2.0 max. 0.5 max. 7 min. 92 max. 4 PALMERA B1220(E) Stearic Acid 92% 194-201 195-202 max. 1.0 66-69 max. 3.0 max. 0.5 100 max. 8.0 92-96 max. 1.5 PALMERA B1220(E) Stearic Acid 95 - 96% 194.0-200.0 195.0-201.0 max. 1.0 66.5-68.5 max. 3.0 max. 0.3 max. 4.0 min. 95.5 max. 1.0 max. 2.0 PALMERA B1220(E) Stearic Acid 98 - 100% 195-200 max. 2 68.0-69.5 max. 2.0 max. 0.5 max. 1.5 min. 98.0 max. 1.0 PALMERA B1220(E) Arachidic Acid 50% 160-190 max. 5 max. 110 max. 17 max. 4 max. 48 40-70 3.5-30.0 PALMERA B1220(E) Arachidic / Behenic Acid 170-178 171-179 max. 3.0 max. 20.0 max. 2.0 max. 4 8-12 37-45 38-48 max. 4 PALMERA B1220(E) Erucic Acid 85% 163-168 75-81 29.5-32.5 max. 7.0 max. 1.0 max. 1.5 85.0-95.0 PALMERA B1220(E) Erucic Acid 90-92% 163-168 164-169 72-79 29.5-32.5 max. 7.0 max. 1.0 max. 3.0 90.0-95.0 max. 2.0 max. 1.5 PALMERA B1220(E) Erucic Acid 163-168 75-81 29.5-32.5 max. 7.0 max. 1.0 max. 1.5 92.0-94.0 PALMERA B1220(E) Behenic Acid 85 - 90% 162-168 163-169 max. 2 75.0-79.0 max. 7.0 max. 1.0 max. 1.0 max. 3.5 max. 9.0 85.0-89.0 max. 3.0 PALMERA B1220(E) Behenic Acid 93 - 94% 160-166 161-167 max. 2 75.0-79.0 max. 4.0 max. 1.0 ← max. 3 max. 5.0 93.5-96.0 max. 4.0 → PALMERA B1220(E) Stearic Acid (Long Cain) 178-190 179-191 max. 3 58-65 max. 15.0 max. 1.5 4-15 29-40 max. 1 50-65 PALMERA B1220(E) Low IV Topped Coconut Fatty Acid 250-260 251-261 max. 1.0 28-32 max. 2.0 max. 0.3 max. 60 max. 1.0 50-56 18-25 8-13 8-15 max. 1.0 PALMERA B1220(E) Distilled Hydrogenated Coconut Fatty Acid 267-275 269-277 max. 0.5 23-29 max. 1.3 max. 0.3 max. 0.05 6.5- 9.0 6.0- 8.0 45.0-55.0 17.0-20.0 7.0-12.0 7.0-14.0 max. 0.5 → PALMERA B1220(E) Hydrogenated Topped Lauric Fatty Acids 251-260 252-261 max. 1 29-33 max. 2.0 max. 0.5 max. 1.5 50-62 15-26 8-14 7-14 max. 1 PALMERA B1220(E) Part Hardened Fatty Acid 205-212 206-213 38-43 44-48 max. 5 max. 0.5 ← max. 0.5 max. 2.0 40.0-48.0 10.0-16.0 37.0-43.0 max. 2.5 PALMERA B1220(E) Part Hardened Fatty Acid 202-210 203-211 32-35 max. 5 max. 0.5 max. 1 max. 1 40-60 20-30 20-30 max. 6.0 PALMERA B1220(E) Mixed Fatty Acid 202-208 202-210 53-64 38-42 max. 12.0 max. 1.5 ← max. 1 max. 3 21-29 13-18 39-45 4-9 PALMERA B1220(E) Distilled Coconut Fatty Acid 265-275 264-276 7.0-11.0 22-26 max. 5.0 max. 0.7 max. 125 max. 0.5 4.0-8.0 5.0-8.0 46.0-53.0 15.0-21.0 7.0-12.0 0.5-3.0 5.0-9.0 max. 2.0 max. 1.0 → PALMERA B1220(E) Distilled Coconut Fatty Acid 264-275 265-276 6-12 22-26 max. 10.0 max. 1.5 5.0-10.0 4.0-8.5 45.0-56.0 15.0-21.0 8.0-13.0 0.5-3.0 3.0-9.0 max. 3.0 max. 1.0 → PALMERA B1220(E) Topped Coconut Fatty Acid 254-263 255-264 8-11 25-29 max. 3.5 max. 0.8 ← max. 1.5 51-58 21-24 9-13 1-5 5-9 1-3 max. 1 → PALMERA B1220(E) Topped Palm Kernel Fatty Acid 244-254 244-255 16-21 25-28 max. 3.0 max. 0.5 max. 0.1 max. 1.5 40.0-60.0 14.0-20.0 6.0-12.0 max. 5.0 12.0-22.0 max. 5.0 → PALMERA B1220(E) Distilled Palm Fatty Acid 206-211 207-212 48-58 43-48 max. 10 max. 1 max. 3 42-48 2-8 35-41 8-12 PALMERA B1220(E) Distilled Palm Oil Fatty Acid 204-210 205-211 46-56 42-48 max. 3.0 max. 0.5 max. 100 max. 4.0 40-48 3-9 35-44 7-12 max. 0.5 PALMERA B1220(E)Palm Kernel Based Heavy End Fatty Acid 200-208 57-65 35-41 max. 10 max. 1.5 ← max. 3.5 26.0-35.0 max. 12.0 min. 45.0 max. 15.0 max. 2.0 → PALMERA B1220(E) Distilled PFAD 206-211 48-58 43-48 max. 15 max. 1 max. 3 42-48 2-8 35-41 8-12 Distilled Fatty Acids Distilled fatty acids are produced from vegetable oils via splitting and distillation/topping and may be offered in their natural form or as (part) hardened. The most common types of distilled fatty acids include palm oil fatty acid, topped palm kernel fatty acid and distilled coconut type fatty acid. Palm stearine fatty acid and palm oil fatty acid mainly consist of C16 and C18 chains. They are used in e.g. production of fatty acid alkanolamides or (methyl) esters, imidazolines, fatty amines, anionic specialty surfactants, alkyd resins for paints and in toiletry, laundry, liquid and transparent soap. Also the plastic and rubber industry uses these fatty acids. Palm kernel fatty acids are offered as 8-18 and as 12-18, hydrogenated and non-hydrogenated. Their main use is in detergents, cleaning and personal care applications. Coconut fatty acid type is also available in the 8-18 and 12-18 types, hydrogenated and non-hydrogenated. The main application is for derivatives manufacturing including esters, fatty amines, anionic specialty surfactants but also alkyd resins for paints and soap production. PALMERA B1220(E)Stearic Acid 204-213 205-214 max. 1.0 54.0-56.0 max. 1.3 max. 0.5 max. 1 max. 2 57.0-65.0 35.0-43.0 max. 2 → PALMERA B1220(E)Triple Pressed Stearic Acid 206-212 207-213 max. 0.5 54-57 max. 2.0 max. 0.2 max. 2.0 55-60 39-45 max. 1.0 PALMERA B1220(E) Stearic Acid 205-210 max. 1.0 55-57 max. 1.5 max. 0.4 max. 3.0 42.0-49.0 47.0-56.0 max. 2.0 PALMERA B1220(E)Stearic Acid 205-210 206-211 max. 1 54-56 max. 1.5 max. 0.4 ← max. 2.0 max. 3 40-52 45-54 max. 2 → PALMERA B1220(E) Stearic Acid 200-210 202-212 max. 5 53-59 max. 15.0 max. 2.0 PALMERA B1220(E) Stearic Acid 205-215 197-217 max. 1.0 52-58 max. 1.5 max. 0.4 ← max. 2 70-85 PALMERA B1220(E) Stearic Acid 202.0-206.0 203.0-207.0 max. 1.0 58-61 max. 2.0 max. 0.3 max. 0.1 max. 2 30.0-35.0 63.0-68.0 max. 1 max. 1 PALMERA B1220(E) Stearic Acid 201-209 202-210 max. 1 56-59 max. 1.0 max. 0.4 max. 1.0 max. 1.5 36.0-40.0 56.0-60.0 max. 1 max. 1.5 PALMERA B1220(E) Stearic Acid 208-212 max. 1.0 52.0-56.0 max. 1.0 max. 0.3 max. 4 49-55 40-47 PALMERA B1220(E)Stearic Acid 205-210 206-211 max. 1 54-56 max. 1.5 max. 0.4 ← max 2.0 2.0-3.0 40-52 45-54 max. 2 → PALMERA B1220(E) Distilled Palm Kernel Fatty Acid/Oleic Acid 215-225 216-226 59-69 max. 10.0 max. 1.5 20-26 5-11 5-11 max. 4 42-50 8-14 max. 1 → PALMERA B1220(E) Stearic Acid 55% 204-210 205-211 max. 0.7 55.5-57.5 max. 3.0 max. 0.3 max. 2.0 41-47 52-58 max. 1.0 PALMERA B1220(E) Mixed Fatty Acid 206-212 207-213 max. 3.0 54.0-59.0 max. 10 max. 1 3.0-4.5 3.0-4.5 26.0-33.0 55.0-65.0 max. 2.0 → Stearic Acids Fatty Acids Stearic Acids and Oleic Acids Stearic acid and oleic acid mainly exist of a mixture of C16 and C18 acids. Stearic acids are completely saturated and solid at room temperature, and oleic acid contains unsaturation being liquid at room temperature. They can be derived from feedstocks such as palm stearin, palm oil and palm kernel oil, but also from european crops like rapeseed oil. All stearines and oleins offered by KLK Emmerich Site are non GMO and kosher. They can be made available under Mass Balance under RSPO conditions. i The main application areas of stearins and oleins include: › Ester and fatty alcohol production › Fatty acid derivatives such as isethionates and sarcosinates › Surfactants in personal care products, liquid and transparent soaps › Corrosion/rust inhibitor for antifreeze › Agricultural chemicals › Adhesives, coatings and inks › Waxes for crayons, candles and leather › Cements › Lubricants and metal working fluids › Plastic and rubber › Textiles etc. PALMERA B1220(E)Oleic Acid 195-203 196-204 min. 86 max. 8.5 max. 225 min. 75 max. 13 PALMERA B1220(E) Low Odour Oleic Acid 194-203 194-204 93-100 max. 10 max. 1 max. 10 max. 0.5 max. 4.0 max. 2.0 75-85 10-18 max. 0.2 max. 1 PALMERA B1220(E) Oleic Acid 195-203 196-204 90-100 max. 7.5 max. 12.0 max. 1.5 max. 200 min. 70 max. 18 PALMERA B1220(E) Distilled Vegetable Fatty Acid 193.0-203.0 194.0-204.0 120.0-145.0 max. atty Acids Fatty acids are produced by splitting fats and oils to give fatty acid and glycerine. MKR is the authorised UK distributor for Palm Oleo, who produces Palmera B1220(E)brand fatty acids which are manufactured from palm oil. There is a wide range of applications for fatty acids including: Plastics and rubber Pharmaceuticals Soaps and detergents Crayons and candles Cosmetics Food additives Varnishes and paints Synthetic lubricants and cutting oils Palmera B1220(E)meaning in Hindi : Get meaning and translation of Palmera B1220(E)in Hindi language with grammar,antonyms,synonyms and sentence usages. Know answer of question : what is meaning of Palmera B1220(E)in Hindi? Palmera B1220(E) ka matalab hindi me kya hai (Palmera B1220(E)). Palmera B1220(E)meaning in Hindi (हिन्दी मे मीनिंग ) is खजूर का वृक्ष.English definition of Palmera B1220(E): Tags: Hindi meaning of Palmera B1220(E), Palmera B1220(E) meaning in hindi, Palmera B1220(E) ka matalab hindi me, Palmera B1220(E) translation and definition in Hindi language.Palmera B1220(E)| Palmera B1220(E) (KLK Oleo Company) having a carbon distribution by weight of 5.33% C8, 6.38% Cio, 51.13% C12, 17.66% Cw, 7.43% C16, 1.74% Cu, 7.63% Ci, i and 1.1% Ci82 2 : Palmera B1220(E) (KLK Oleo Company) having a carbon distribution by weight of 0.71% Cio, 52.26% Ci2, 17.32% d4, 9.36% C16, 2.34% Ci8, 15.40% C18i and 2.25% C„2 3 : Palmera B1220(E) (KLK Oleo Company) having a carbon distribution by weight of 5.61% C8, 8.59% C10, 49.54% Ci2, 17.75% Cu, 8.28% Ci6 and 8.41% C18
PALMERA IS 10
CAS Number: 30399-84-9
Molecular Formula: C18H36O2
Molecular Weight: 284.47700




APPLICATIONS

Palmera IS 10 is a lightly-branched, liquid fatty acid produced by the reaction of oleic acid with a natural mineral catalyst.
There is no chemical addition in this reaction, isostearic acid is based 100% on the parent oil or fat.
Palmera IS 10 is used in applications which require a liquid fatty acid with exceptional stability: thermal stability in the case of a lubricant, odour stability for a cosmetic formulation, and oxidation stability for products with long shelf-life requirements.

The branching structure of Palmera IS 10 also enhances its dispersing power.
Palmera IS 10 is used in cosmetic and industrial applications for the stabilisation of pigments and mineral particles in oils and solvents.

Palmera IS 10 is an exceptionally mild liquid fatty acid that offers a light lubricious feel and can be used in many skin care and colour cosmetic applications.
Further, Palmera IS 10 also offers film forming properties, making it ideal for use in soaps, shaving foams and liquid cleansers.

Palmera IS 10 can be used as:

Opacifer
Softener and conditioner

Being a fatty acid, Palmera IS 10 is also amphiphilic, meaning it is a molecule with a hydrophobic end and a hydrophilic end.
As such, Palmera IS 10 can have favorable interactions with both polar and non-polar molecules, enabling it to act as a surfactant.

Palmera IS 10 is also soluble in many oils, which allows it to be used as an emulsifier or dispersant.
With this set of properties, Palmera IS 10 is a useful additive in a variety of applications.

Palmera IS 10 is used in applications which require a liquid fatty acid with exceptional stability: thermal stability in the case of a lubricant, odour stability for a cosmetic formulation, and oxidation stability for products with long shelf-life requirements.
The branching structure of Palmera IS 10 also enhances its dispersing power, and it is used in cosmetic and industrial applications for the stabilisation of pigments and mineral particles in oils and solvents.

Palmera IS 10 can be used as:

Surface modifier
Surfactant (surface active agent)
Swelling agent

Palmera IS 10 is used as emulsifier.
Moreover, Palmera IS 10 is used as surfactant.
Palmera IS 10 can be used as cleansing Agent.

Palmera IS 10 can be used in decorative cosmetics.
Furthermore, Palmera IS 10 can be used in fragrances.

Palmera IS 10 can be used in hair care.
Moreover, Palmera IS 10 can be used in skin care.
Palmera IS 10 can be used in toiletries.



DESCRIPTION


Palmera IS 10 is used in the production of TMP esters which are further used in lubricant applications.
Further, Palmera IS 10 exhibits good oxidative stability and offers excellent low temperature properties.
Palmera IS 10 finds application in transparent soaps.

PALMERA Distilled and Fractionated Fatty Acids are produced in accordance with the required demands and quality standards such as GMP and HACCP – making them suitable for food, pharmaceutical and personal care applications.
Palmera IS 10 can be used as-is, or as a derivative.

Fatty Acids may be found in plastics, rubber, textiles, lubricants, metal-working, crayons, candles, biocides, paints, inks and etc.
Palmera IS 10 is a lightly-branched, liquid fatty acid produced by the reaction of oleic acid with a natural mineral catalyst – there is no chemical addition in this reaction, Palmera IS 10 is based 100% on the parent oil or fat.

Palmera IS 10 is used in applications which require a liquid fatty acid with exceptional stability: thermal stability in the case of a lubricant, odour stability for a cosmetic formulation, and oxidation stability for products with long shelf-life requirements.
The branching structure of Palmera IS 10 also enhances its dispersing power, and it is used in cosmetic and industrial applications for the stabilisation of pigments and mineral particles in oils and solvents.



PROPERTIES


a) Physical state: powder
b) Color: No data available
c) Odor: No data available
d) Melting point/freezing point: No data available
e) Initial boiling point and boiling range: No data available
f) Flammability (solid, gas): No data available
g) Upper/lower flammability or explosive limits: No data available
h) Flash point: No data available
i) Autoignition temperature: No data available
j) Decomposition temperature: No data available
k) pH: No data available
l) Viscosity:
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
m) Water solubility: No data available
n) Partition coefficient: n-octanol/water No data available
o) Vapor pressure: No data available
p) Density: No data available
Relative density: No data available
q) Relative vapor density: No data available
r) Particle characteristics: No data available
s) Explosive properties: No data available
t) Oxidizing properties: none


Chemical Properties of Palmera IS 10:

Boiling Point: 359.4ºC at 760mmHg
Molecular Formula: C18H36O2
Melting Point: 69.3ºC
Density: 0.888g/cm3
Boiling Point: 359.4ºC at 760mmHg
Melting Point: 69.3ºC
Molecular Formula: C18H36O2
Molecular Weight: 284.47700
Flash Point: 162.4ºC
Exact Mass: 284.27200
PSA: 37.30000
LogP: 6.18840
Flash Point: 162.4º



FIRST AID


Description of first-aid measures:

If inhaled:

If breathed in, move person into fresh air.
If not breathing, give artificial respiration.

In case of skin contact:

Wash off with soap and plenty of water.

In case of eye contact:

Flush eyes with water as a precaution.

If swallowed:

Never give anything by mouth to an unconscious person.
Rinse mouth with water.



HANDLING AND STORAGE


Precautions for safe handling:

Advice on protection against fire and explosion:

Provide appropriate exhaust ventilation at places where dust is formed.

Hygiene measures:

General industrial hygiene practice.

Conditions for safe storage, including any incompatibilities:

Storage conditions:

Keep container tightly closed in a dry and well-ventilated place.
Store in cool place.
Storage stability
Recommended storage temperature: -20 °C

Prohibitions on mixed storage:

Keep Substance Away From:

Ignition sources.
(Strong) acids.
(Strong) bases.

Storage area:

Keep container in a well-ventilated place.
Store at ambient temperature.
Keep out of direct sunlight.
Meet the legal requirements.

Special rules on packaging:

Special Requirements:

Closing.
Correctly labelled.
Meet the legal requirements.

Packaging materials:

Suitable Material:

Steel with plastic inner lining.
Stainless steel.
Aluminum.

Storage class (TRGS 510): 13: Non Combustible Solids



SYNONYMS


Aliphatic acid
mixture of straight chain and methyl-branched C18
saturated acids
isooctadecanoic acid
emersol875
emery871
century1105
emersol871
prisorine3502
875d
emery875d
Iso- Octadecansäure
prisorine3508
prisorine3501
Isostearic acid
Isostearic acid 873
Isostearic acid EX
Jaric I 18CG
Jaric I 18IG
Prisorin ISAC 3505
Prisorine 3501
Prisorine 3502
Prisorine 3505
Prisorine 3508
UCN 96.319
Unimac 5680
Isooctadecanoic acid
Isostearic acid
Emery 875D
875D
Emersol 875




PALMERA IS 20



APPLICATIONS



Palmera IS 20 is used for chemicals added that influence or buffer ph.
Further, Palmera IS 20 can be used for flavouring.
Palmera IS 20 is used for fragrance.

Palmera IS 20 is used for fragrance component.
Moreover, Palmera IS 20 can be used for freeze protectant.

Palmera IS 20 is used for is products intended for pet care which do not fit into a more refined category.
More to that, Palmera IS 20 is used for miscellaneous pet treatments (excluding pesticides and shampoos).

Palmera IS 20 can be used for pet shampoos (including those containing pesticides, such as flea/tick shampoos).
Beside that, Palmera IS 20 is used for care products specifically for cats which do not fit into a more refined category.
Palmera IS 20 is used for preservative.

Used as a fungicide, herbicide and emulsifying agent; Palmera IS 20 occurs naturally in cheese and is an approved food preservative.
Palmera IS 20 is chemical intermediate for calcium, sodium propionates, cellulose propionate plastics, plasticizers, pharmaceuticals.

Palmera IS 20 is chemical intermediate for the herbicides dalapon, erbon, and propanil; grain preservative.
Beside that, Palmera IS 20 is used for adhesion/cohesion promoter.

Palmera IS 20 is used for agricultural chemicals (non-pesticidal).
Further, Palmera IS 20 is used as intermediate.
Palmera IS 20 is used as preservative.

Palmera IS 20 is used for processing aids.
More to that, Palmera IS 20 is used for agricultural chemicals (non-pesticidal).



DESCRIPTION


Palmera IS 20 is used in the production of TMP esters which are further used in lubricant applications.
Furthermore, Palmera IS 20 offers excellent low temperature properties and exhibits good oxidative stability.
Palmera IS 20 is used in transparent soaps.

Palmera IS 20 is a colorless liquid with a sharp rancid odor.
More to that, Palmera IS 20 produces irritating vapor.

Palmera IS 20 can be obtained from wood pulp waste by fermentation process using bacteria of the genus Propionibacterium.

Palmera IS 20 is a short-chain saturated fatty acid comprising ethane attached to the carbon of a carboxy group.
Moreover, Palmera IS 20 has a role as an antifungal drug.
Palmera IS 20 is a short-chain fatty acid and a saturated fatty acid.

Palmera IS 20 is a conjugate acid of a propionate.
Further, Palmera IS 20 is the sodium salt of propionic acid that exists as colorless, transparent crystals or a granular crystalline powder.

Palmera IS 20 is considered generally recognized as safe (GRAS) food ingredient by FDA, where it acts as an antimicrobial agent for food preservation and flavoring agent.
The use of Palmera IS 20 as a food additive is also approved in Europe.
Palmera IS 20 is prepared by neutralizing propionic acid with sodium hydroxide.

Palmera IS 20 was previously approved in Canada as an active ingredient in Amino-Cerv (used to treat inflammation or injury of the cervix).

Relatively unreactive organic reagents should be collected in container A.
If halogenated, they should be collected in container B.
For solid residues use container C.



PROPERTIES


Molecular Weight: 74.08
XLogP3: 0.3
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 1
Exact Mass: 74.036779430
Monoisotopic Mass: 74.036779430
Topological Polar Surface Area: 37.3 Ų
Heavy Atom Count: 5
Formal Charge: 0
Complexity: 40.2
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Boiling point: 229 °C (1013 hPa)
Density: 0.887 g/cm3 (20 °C)
Explosion limit: 0.9 - 6.0 %(V)
Flash point: 86 °C
Ignition temperature: 230 °C
Melting Point: -90 °C
Vapor pressure: 0.12 hPa (20 °C)
Solubility: 0.1 g/l



FIRST AID


Description of first-aid measures

General advice:

Consult a physician.
Show this material safety data sheet to the doctor in attendance.

If inhaled:

If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.

In case of skin contact:

Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:

Flush eyes with water as a precaution.

If swallowed:

Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.



STORAGE AND HANDLING


Precautions for safe handling:

Advice on safe handling:

Avoid inhalation of vapor or mist.

Advice on protection against fire and explosion:

Keep away from sources of ignition.
No smoking.
Take measures to prevent the build up of electrostatic charge.

Hygiene measures:

Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.


Conditions for safe storage, including any incompatibilities:

Storage conditions:

Keep container tightly closed in a dry and well-ventilated place.
Store in cool place.

Storage class (TRGS 510): 2A: Gases



SYNONYMS


propionic acid
Propanoic acid
79-09-4
ethylformic acid
methylacetic acid
Carboxyethane
Metacetonic acid
Ethanecarboxylic acid
Pseudoacetic acid
Luprosil
Monoprop
propionate
Prozoin
Antischim B
Propionoic acid
Acide propionique
Methyl acetic acid
Sentry grain preserver
C3 acid
Tenox P grain preservative
Caswell No. 707
Propionic acid grain preserver
FEMA No. 2924
Propionsaeure
Propcorn
Propkorn
propoic acid
Propioic acid
acide propanoique
Propionic acid (natural)
Kyselina propionova
Carboxylic acids, C1-5
Acide propionique [French]
Kyselina propionova [Czech]
CCRIS 6096
proprionic acid
C1-5 Carboxylic acids
EPA Pesticide Chemical Code 077702
Fatty acids, C3-24
HSDB 1192
n-propionic acid
Toxi-Check
AI3-04167
CH3-CH2-COOH
UN1848
BRN 0506071
Propionic acid [NF]
CHEBI:30768
JHU490RVYR
CHEMBL14021
INS NO.280
68937-68-8
INS-280
metacetonate
propanate
pseudoacetate
ethanecarboxylate
68990-37-4
Propionic acid (NF)
Propionic acid [UN1848] [Corrosive]
E-280
Propionic acid, >=99.5%
Propanyl acid
FEMA Number 2924
EINECS 201-176-3
UNII-JHU490RVYR
MFCD00002756
Luprisol
proponic acid
1-propanoic acid
2-methylacetic acid
EINECS 273-079-4
EtCO2H
Propionic acid solution
Propionic acid, 99%
Propanoic acid (9CI)
C2H5COOH
DSSTox_CID_5961
bmse000179
Epitope ID:139981
Propionic acid, >=99%
Propionic acid, 99.5%
EC 201-176-3
PROPIONIC ACID [MI]
DSSTox_GSID_25961
Propionic Acid Reagent Grade
NATURAL PROPIONIC ACID
Propionic acid (6CI,8CI)
PROPIONIC ACID [FCC]
4-02-00-00695 (Beilstein Handbook Reference)
Propionic acid, 99%, FCC
PROPIONIC ACID [FHFI]
PROPIONIC ACID [HSDB]
PROPIONIC ACID [INCI]
PROPIONIC ACID [VANDF]
GTPL1062
PROPIONIC ACID [MART.]
DTXSID8025961
PROPIONIC ACID [USP-RS]
PROPIONIC ACID [WHO-DD]
AMY4114
Top distillation cut by-product acids, monobasic (C1-C5)
Methylacetic Acid, Propanoic Acid
Propionic acid, ACS reagent grade
Carboxymethoxylaminehemihydrochloride
Propionic acid, analytical standard
ZINC6050663
Propionic acid, natural, 99%, FG
Tox21_304030
BDBM50082199
LMFA01010003
STL168039
Propionic acid, feed grade, 98.7%
AKOS000118853
DB03766
UN 1848
CAS-79-09-4
Propionic acid, for synthesis, 99.5%
NCGC00357239-01
Propionic acid, >=99.5%, FCC, FG
BP-20411
E280
Propionic acid 100 microg/mL in Ethanol
Propionic acid, ACS reagent, >=99.5%
FT-0637136
FT-0658557
P0500
Propionic acid 100 microg/mL in Cyclohexane
Propionic acid, SAJ first grade, >=98.0%
C00163
D02310
Propionic acid 1000 microg/mL in Acetonitrile
Propionic acid, puriss. p.a., >=99.5% (GC)
Q422956
F2191-0098
Propionic acid, BioReagent, suitable for insect cell culture, ~99%
Propionic acid, United States Pharmacopeia (USP) Reference Standard










PALMERA IS 30
APPLICATIONS


Palmera IS 30 can be used as emulsifier.
Palmera IS 30 is used as surfactant/ cleansing agent.

Some uses of Palmera IS 30:

Decorative cosmetics
Fragrances
Hair care
Skin care
Toiletries

Palmera IS 30 is used for paints or sealers for treating fabrics.
More to that, Palmera IS 30 is used for shellacs or polyurethane coatings for primarily craft purposes.

Palmera IS 30 can be used in writing utensils containing liquid or gel ink.
Moreover, Palmera IS 30 can be used in products used for cleaning or safety in an occupational or industrial setting (e.g. industrial cleaning supplies or laundry detergent, eye wash, spill kits) .
Palmera IS 30 is used in cleaning and household care products that can not be placed in a more refined category.

Palmera IS 30 is used in bathtub, tile, and toilet surface cleaners.
Further, Palmera IS 30 is used in products that impart a shine to solid floors.
Palmera IS 30 is used for cleaning products for general household cleaning, which do not fit into a more refined category.

Palmera IS 30 is used for products that remove stains or discoloration of fabric (including color-safe bleaches) used in laundry.
Beside that, Palmera IS 30 is used for products used to clean glass, mirrors, and windows.

Palmera IS 30 is used in heavy duty hard surface cleaning products that may require dilution prior to use (i.e., may be concentrated).
Moreover, Palmera IS 30 is used in products used in washing machines to clean fabrics.

Palmera IS 30 is used in products used to polish metal surfaces.
Further, Palmera IS 30 can be used in products applied to footwear to color, polish, clean, or add a protective surface.

Palmera IS 30 can be used as dispersing agent.
Furthermore, Palmera IS 30 can be used as emollient.

Palmera IS 30 can be used as emulsifier.
Furthermore, Palmera IS 30 can be used as flavouring.
Palmera IS 30 can be used as fragrance.

Palmera IS 30 can be used as fragrance component.
Further, Palmera IS 30 can be used in general formulation products used for home maintenance, which do not fit into a more refined category.
Palmera IS 30 can be used in products applied to hard surfaces to remove paints and finishes.

Palmera IS 30 is used in miscellaneous welding products including gases, fluxes, and adhesives.
Moreover, Palmera IS 30 is used in formulations used as part of a process, or in a piece of equipment (e.g. lubricants, adhesives, sealants, oils, paints, coatings).

Palmera IS 30 is used in antibacterial products for application to hands.
More to that, Palmera IS 30 is used in liquid hand soaps.

Palmera IS 30 is used in deodorants and antiperspirants.
Further, Palmera IS 30 is used in facial cleansing products containing exfoliating particles (excluding products for acne).
Palmera IS 30 is used in general hair coloring products which can not be classified into a more refined category.

Palmera IS 30 is used in general hair styling or hair care products which do not fit into a more refined category.
Moreover, Palmera IS 30 can be used for rinse-out everyday hair conditioners (excluding combo shampoo/conditioner products).

Palmera IS 30 can be used for products for imparting hold, shine, or texture to hair.
Beside that, Palmera IS 30 is used in make-up or cosmetic products which do not fit into a more refined category.

Palmera IS 30 can be used for foundation make-up and concealers.
Furthemore, Palmera IS 30 is used in lip products primarily for protection.
Palmera IS 30 is used in glossy lip products.

Palmera IS 30 is used in eyelash mascaras.
More to that, Palmera IS 30 is used in pure chemicals or ingredients.
Palmera IS 30 is used as solublizer.

Palmera IS 30 is used as solvent.
Moreover, Palmera IS 30 is used as surface conditioner.
Palmera IS 30 is used as surfactant.

Palmera IS 30 is used to make soaps and detergents, to prepare turkey red oil, and to waterproof fabrics
Further, Palmera IS 30 is also used in polishing compounds, oiling wool, thickening lubricating oils, anionic and nonionic surfactants, plasticizers, waxes, ointments, cosmetics, and food-grade additives; Other uses are ore flotation, rodent extermination, and defoaming.

Palmera IS 30 is defoaming agent in wet-process phosphoric acid process
Further, Palmera IS 30 can be used as abrasives
Palmera IS 30 can be used as adhesives and sealant chemicals

Palmera IS 30 can be used as agricultural chemicals (non-pesticidal)
More to that, Palmera IS 30 can be used as corrosion inhibitor

Palmera IS 30 can be used as emulsifier
Moreover, Palmera IS 30 can be used as finishing agents

Palmera IS 30 can be used as flotation agent
Beside that, Palmera IS 30 can be used as foamant
Palmera IS 30 can be used as fuel

Palmera IS 30 is a monounsaturated omega-9 fatty acid.
Further, Palmera IS 30 is obtained by the hydrolysis of various animal and vegetable fats and oils.
Palmera IS 30 is used as an emulsifying or solubilizing agent in aerosol products.

Palmera IS 30 can be used in paint additives and coating additives not described by other categories.
Furthermore, Palmera IS 30 can be used as pigment.
Palmera IS 30 can be used in processing aids, not otherwise listed.

Palmera IS 30 is also known as omega-9.
Furthermore, Palmera IS 30 can improve the skinpenetration abilities of a preparation’s other components.
Palmera IS 30 is an essential fatty acid.

Palmera IS 30 is obtained from various animal and vegetable fats and oils, and may be mildly irritating to the skin.



DESCRIPTION


Palmera IS 30 is used in the production of TMP esters which are further used in lubricant applications.
Further, Palmera IS 30 offers excellent low temperature properties and exhibits good oxidative stability.
PALMERA IS-30 finds application in transparent soaps.

Palmera IS 30 is a cis-unsaturated fatty acid that has been shown to activate protein kinase C in hepatocytes.
More to that, Palmera IS 30 potentiates acetylcholine receptor currents by activating CaM kinase II, independent of the PKC pathway.
Unsaturated fatty acid that has been shown to activate protein kinase C in hepatocytes.
Density of Palmera IS 30 is 0.89 g/ml.

Palmera IS 30 is a colorless to pale yellow liquid with a mild odor.
Further,Palmera IS 30 floats on water.

Palmera IS 30 is an octadec-9-enoic acid in which the double bond at C-9 has Z (cis) stereochemistry.
Furthermore, Palmera IS 30 has a role as an EC 3.1.1.1 (carboxylesterase) inhibitor, an Escherichia coli metabolite, a plant metabolite, a Daphnia galeata metabolite, a solvent, an antioxidant and a mouse metabolite.
Palmera IS 30t is a conjugate acid of an oleate. It derives from a hydride of a cis-octadec-9-ene.

Palmera IS 30 is a natural product found in Gladiolus italicus, Prunus mume, and other organisms with data available.

This carboxylic acid, also known as Palmera IS 30, presents as a colorless to yellow liquid.
Palmera IS 30 is known to be soluble in many organic solvents and miscible in methanol, acetone and carbon tetrachloride.

Palmera IS 30 is also insoluble in water.
For best results, keep container of Palmera IS 30 tightly closed.
Store in a refrigerator, under inert gas - this substance is heat sensitive, air sensitive and light sensitive.

Palmera IS 30 is incompatible with oxidizing agents and strong bases.
More to that, Palmera IS 30 causes skin irritation and eye irritation.

Palmera IS 30, a monounsaturated fatty acid originally derived from Olea europaea, has been shown to be an anti-proliferative agent.
Moreover, Palmera IS 30 has also been reported to promote neuronal differentiation in murine cell cultures.

Mechanistic studies suggest that these Palmera IS 30 effects are mediated by PPARβ.
Furthermore, Palmera IS 30 has demonstrated the ability to stimulate an increase in secretion of collagen I, TGF-β secretion, and extracellular signal-regulated kinase1/2.
Palmera IS 30 Acid is an activator of PKC and CaMKII.



PROPERTIES


Purity / Analysis Method: >99.0%(GC)(T)
Molecular Formula / Molecular Weight: C18H34O2 = 282.47
Physical State (20 deg.C): Liquid
Storage Temperature: 0-10°C
Store Under Inert Gas: Store under inert gas
Condition to Avoid: Light Sensitive,Air Sensitive,Heat Sensitive
assay: ≥99% (GC)
Molecular Weight: 282.5
XLogP3 6.5: Computed by XLogP3 3.0
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 15
Exact Mass: 282.255880323
Monoisotopic Mass: 282.255880323
Topological Polar Surface Area: 37.3 Ų
Heavy Atom Count: 20
Formal Charge: 0
Complexity: 234
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 1
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
form: liquid
storage condition: OK to freeze
color: colorless
solubility:
chloroform: 10 mg/mL
ethanol: 5 mg/mL
density: 0.89 g/mL
storage temp.: 2-8°C



FIRST AID


Description of first-aid measures:

If inhaled:

After inhalation: fresh air.

In case of skin contact

In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.

In case of eye contact

After eye contact:
Rinse out with plenty of water.
Remove contact lenses.

If swallowed

After swallowing:
make victim drink water (two glasses at most).
Consult doctor if feeling unwell.



STORAGE AND HANDLING


Conditions for safe storage, including any incompatibilities

Storage conditions:
Protected from light.
Tightly closed.
Store at +2°C to +8°C.



SYNONYMS


cis-9-Octadecenoic Acid
oleic acid
112-80-1
cis-9-Octadecenoic acid
oleate
(Z)-Octadec-9-enoic acid
ALDEHYDE C1
FORMALDE-FRESH
FORMALDE-FRESH SOLUTION
FORMALDE-FRESH SOLUTION, BUFFERED
FORMALDEHYDE
FORMALDEHYDE, BUFFERED
FORMALDEHYDE, CARSON-MILLON
FORMALDEHYDE DEVELOPING SOLUTION
FORMALDEHYDE SOLUTION
FORMALDEHYDI
FORMALIN
FORMALIN, CARSONS
FORMALIN, NEUTRAL
FORMALIN NEUTRAL BUFFER
FORMALIN, NEUTRAL BUFFERED
FORMALIN NEUTRAL SODIUM SALT
FORMIC ALDEHYDE
FORMOL
METHANAL
METHANONE
Elaidoic acid
cis-Oleic acid
9-Octadecenoic acid (Z)-
Δ9-cis-Oleic acid
cis-Oleic Acid
cis-9-Octadecenoic Acid
Emersol 211; Emersol 220 White Oleic Acid
Emersol 221 Low Titer White Oleic Acid
Oelsauere; Oleine 7503
Pamolyn 100
Vopcolene 27; Wecoline OO
Z-9-Octadecenoic acid
cis-Octadec-9-enoic acid
cis-Δ9-octadecenoic acid
cis-Δ9-Octadecenoate
neo-Fat 90-04
neo-Fat 92-04; Century cd fatty acid
Elaidoic acid; Emersol 210
Emersol 213; Emersol 6321; Glycon RO
Glycon WO
Groco 2
Groco 4
Groco 5l
Groco 6; Hy-phi 1055
Hy-phi 1088; Hy-phi 2066; Hy-phi 2088
Hy-phi 2102; K 52; L'Acide oleique
Metaupon; Tego-oleic 130
9-Octadecenoic acid, cis-; Elaic acid
Industrene 105
Industrene 205; Industrene 206
Oleinic acid; Pamolyn
Wochem no. 320
(Z)-9-Octadecanoic acid
Emersol 6313 NF; Priolene 6906
9-(Z)-octadecenoic acid; (Z)-Octadec-9-enoic acid
9-Octadecenoic acid (9Z)-; D 100
Emersol 205; Extraolein 90
Wecoline OO
Vopcolene 27
Glycon wo
Pamolyn 100
Glycon RO
Metaupon
Oelsauere
Groco 5l
Groco 2
Groco 4
Groco 6
Tego-oleic 130
Emersol 211
9Z-Octadecenoic acid
cis-Octadec-9-enoic acid
Industrene 105
Industrene 205
Industrene 206
Pamolyn
Z-9-Octadecenoic acid
9-Octadecenoic acid (Z)-
Oleinic acid
Emersol 210
Emersol 213
9-Octadecenoic acid (9Z)-
L'Acide oleique
Century cd fatty acid
Emersol 6321
Extraolein 90
Oleine 7503
9-Octadecenoic acid, (Z)-
Emersol 205
Emersol 233LL
Hy-phi 1055
Hy-phi 1088
Hy-phi 2066
Hy-phi 2088
Hy-phi 2102
Elaic acid
Priolene 6906
9-octadecenoic acid
White oleic acid
Wochem no. 320
Emersol 220 white oleic acid
FEMA No. 2815
Extra Oleic 80R
Extra Oleic 90
Extra Oleic 99
Extra Olein 80
Extra Olein 90R
Lunac O-CA
Lunac O-LL
Lunac O-P
neo-Fat 92-04
Priolene 6907
Priolene 6928
Priolene 6930
Priolene 6933
Elainic acid
Emersol 6313NF
cis-Oleate
delta9-cis-Oleic acid
(9Z)-octadec-9-enoic acid
(9Z)-Octadecenoic acid
FEMA Number 2815
D 100 (fatty acid)
Emersol 221 low titer white oleic acid
K 52
Oelsaeure
9-cis-Octadecenoic acid
HSDB 1240
Red oil
D 100
(9Z)-9-Octadecenoic acid
Oleic acid [NF]
9-octadecylenic acid
Emersol 233
OLEICACID
18:1Delta9cis
Priolene 6936
CHEBI:16196
NSC-9856
9,10-Octadecenoic acid
C18:1n-9
neo-Fat 90-04
.delta.9-cis-Oleic acid
9-(Z)-octadecenoic acid
(Z)-9-Octadecanoic acid
9-Octadecenoic acid, cis-
cis-.delta.9-Octadecenoate
2UMI9U37CP
CHEMBL8659
cis-.delta.9-Octadecenoic acid
cis-Delta(9)-octadecenoic acid
NSC9856
Oleic acid (NF)
Osteum
MFCD00064242
C18:1 n-9
FA 18:1
Octadec-9-enoic acid
NCGC00091119-02
18:1 n-9
C18:1
cis-9-octadecenoate
(9Z)- Octadecenoic acid
DSSTox_CID_5809
18:1(n-9)
Oleic acid, pure
DSSTox_RID_77930
DSSTox_GSID_25809
Oleic acid (natural)
Caswell No. 619
Wecoline OO (VAN)
Acide oleique [French]
Acide oleique
cis-delta9-octadecenoic acid
l'Acide oleique [French]
CAS-112-80-1
SMR000326739
CCRIS 682
NAA 35
Sulfurized oleic acid
Sulphurized oleic acid
Oleic acid, sulfurized
cis-delta(sup 9)-Octadecenoic acid
NSC 9856
EINECS 204-007-1
UNII-2UMI9U37CP
EPA Pesticide Chemical Code 031702
BRN 1726542
Distoline
Oleinate
oleaic acid
Rapinic acid
AI3-01291
1gni
1hms
1vyf
2lkk
Oleic acid Liquid
Lunac OA
Edenor ATiO5
Edenor FTiO5
Industrene 104
Z-9-Octadecenoate
EINECS 270-164-8
Oleic acid, p.a.
Emersol 213NF
Emersol 214NF
Pamolyn 125
Priolene 6900
9,10-Octadecenoate
9-Octadecenoic acid (Z)-, sulfurized
Oleic acid (8CI)
oleic acid extra pure
cis-Octadec-9-enoate
Pamolyn 100 FG
Pamolyn 100 FGK
9-(Z)-octadecenoate
Emersol 7021
9-Octadecenoic acid (9Z)-, sulfurized
(Z)-9-Octadecanoate
Emersol 6313 NF
Emersol 6333 NF
Oleic acid-9,10-t
(9Z)-9-Octadecenoate
Emersol 220 White Oleate
OLEIC ACID [VANDF]
Oleic acid, technical grade
SCHEMBL1138
Delta9-cis-Octadecenoic acid
OLEIC ACID [MART.]
WLN: QV8U9-C
OLEIC ACID [USP-RS]
OLEIC ACID [WHO-DD]
4-02-00-01641 (Beilstein Handbook Reference)
99148-48-8
MLS001056779
MLS002153498
MLS002454427
9-octadecenoic acid, (9Z)-
(9Z)-9-Octadecenoic acid
GTPL1054
Oleic acid, analytical standard
DTXSID1025809
Oleic acid, >=93% (GC)
Oleic acid, >=99% (GC)
REGID_for_CID_445639
1g7
OLEIC ACID [EP MONOGRAPH]
HMS2234O13
HMS3649H21
HMS3885H18
Oleic acid, technical grade, 90%
HY-N1446
ZINC6845860
ENDOCINE COMPONENT OLEIC ACID
Tox21_111086
Tox21_201967
Tox21_303324AKOS017343225
cis-.delta.(sup 9)-Octadecenoic acid
AT13415
CCG-267270
9-Octadecenoic-9,10-t2 acid, (Z)-
NCGC00091119-01
NCGC00091119-03
NCGC00257233-01
NCGC00259516-01
68412-07-7
AC-33767
AS-1606
BP-24023
FA(18:19Z))
Oleic acid, SAJ first grade, >=70.0%
Oleic acid, Selectophore(TM), >=99.0%
CS-0016886
O0011
O0180
C00712
D02315
Oleic acid, from suet, natural, >=60% (GC)
AB00641912_08
9-Octadecenoic-9,10-t2 acid, (9Z)- (9CI)
A894525
SR-01000780573
OLEIC ACID (CONSTITUENT OF SPIRULINA) [DSC]
SR-01000780573-6
9-Octadecenoic acid(Z)-,oxidized,sulfonated,sodium salts
F0001-0262
OLEIC ACID (CONSTITUENT OF FLAX SEED OIL) [DSC]
OLEIC ACID (CONSTITUENT OF SAW PALMETTO) [DSC]
Oleic acid, certified reference material, TraceCERT(R)
OLEIC ACID (CONSTITUENT OF BORAGE SEED OIL) [DSC]
Oleic acid, European Pharmacopoeia (EP) Reference Standard
Ole
Oleic acid, PharmaGrade, Manufactured under appropriate controls for use as raw material in pharma or biopharmaceutical production.











PALMESTER 1412 ISOPROPYL OLEATE
Palmester 1412 Isopropyl Oleate is a biodegradable, fatty ester derived from renewable vegetable oils.
Palmester 1412 Isopropyl Oleate acts as a lubricant, viscosity modifier, plasticizer for polymer.
Palmester 1412 Isopropyl Oleate is suitable for internal & external automotive, transportation, appliances, electrical market, household products and consumer goods.

CAS: 112-11-8
MF: C21H40O2
MW: 324.54
EINECS: 203-935-4

Synonyms
9-Octadecenoicacid(Z)-,1-methylethylester;9-Octadecenoic acid (9Z)-, 1-methylethyl ester;Isopropyloleat;(Z)-9-Octadecenoic acid 1-methylethyl ester;Oleic acid isopropyl ester;Isopropyl (Z)-9-octadecenoate;1-methylethyl ester;9-Octadecenoic acid, 1-methylethyl ester;Isopropyl oleate;112-11-8;Oleic acid, isopropyl ester;9-Octadecenoic acid (9Z)-, 1-methylethyl ester;propan-2-yl (Z)-octadec-9-enoate;9-Octadecenoic acid (Z)-, 1-methylethyl ester;Isopropyl 9Z-octadecenoate;4152WNN49V;NSC-50952;WE(2:0(1Me)/18:1(9Z));i-Propyl 9-octadecenoate;UNII-4152WNN49V;EINECS 203-935-4;NSC 50952;AI3-32462;AEC ISOPROPYL OLEATE;EC 203-935-4;isopropyl oleate, AldrichCPR;SCHEMBL61998;1-Methylethyl-9-octadecenoate;ISOPROPYL OLEATE [INCI];PZQSQRCNMZGWFT-QXMHVHEDSA-N;NSC50952;LMFA07010671;9-Octadecenoic acid, 1-methylethyl ester;NS00004593;(2E)-4-[(4-Methoxybenzyl)oxy]-2-buten-1-ol;Q27258396

Recommended for packaging, pipe, hoses & fittings, wiring & cables, building and construction. Palmester 1412 Isopropyl Oleate is KOSHER and HALAL certified.
Palmester 1412 Isopropyl Oleate is prepared by the esterification of oleic acid and isopropanol.
Palmester 1412 Isopropyl Oleate is an ester that is widely used in various fields of research and industry due to its pharmaceutical, cosmetic, and industrial applications.
This paper provides an overview of Palmester 1412 Isopropyl Oleate and its physical and chemical properties, synthesis, characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, and potential implications in various fields of research and industry.
Additionally, this paper explores the limitations of IPO and future directions for research and development.
Palmester 1412 Isopropyl Oleate is an ester composed of isopropyl alcohol and oleic acid.
Palmester 1412 Isopropyl Oleate is a liquid at room temperature, colorless, and odorless in nature.
Palmester 1412 Isopropyl Oleate is commonly used in the pharmaceutical industry as a solvent and penetration enhancer and can also be used in cosmetics and personal care products due to its emollient properties.
Palmester 1412 Isopropyl Oleate has a low viscosity and can penetrate the skin easily, making it beneficial for topical applications.
Additionally, Palmester 1412 Isopropyl Oleate is used as a lubricant in the industrial sector.

Palmester 1412 Isopropyl Oleate is a non-branched mono saturated fatty acid ester obtained from isopropanol and oleic acid, from palm and olive oil.
Clear liquid with a melting point of -12 ºC.
Cosmetic formulations: binding, skin conditioning, emollient.
Industrial uses: manufacturer of washing and cleaning products, polymers, adhesives and sealants, textile treatment products and dyes, lubricants and greases, plant protection products, pH regulators and water treatment products.

Palmester 1412 Isopropyl Oleate Chemical Properties
Melting point: -37.7 °C
Boiling point: 215-217 °C(Press: 14-15 Torr)
Density: 0.8678 g/cm3(Temp: 15 °C)
LogP: 5.79 at 20℃
EPA Substance Registry System: Palmester 1412 Isopropyl Oleate (112-11-8)

Palmester 1412 Isopropyl Oleate is a transparent oily liquid, colorless, odorless, and insoluble in water.
Palmester 1412 Isopropyl Oleate can be used as cosmetics, plasticizers, machinery oil additives and surface wetting agents for dyes, etc.
Palmester 1412 Isopropyl Oleate is composed of isopropyl oleate.
Palmester 1412 Isopropyl Oleate can be used as a lubricant base fluid.
The physical and chemical properties of isopropyl oleate play a crucial role in determining its applications in various fields.
Palmester 1412 Isopropyl Oleate is a colorless, clear liquid with a boiling point of 216°C, a melting point of -39°C, and a density of 0.873 g/cm3.
Palmester 1412 Isopropyl Oleate is highly soluble in various solvents, including alcohols, ethers, and hydrocarbons.
Palmester 1412 Isopropyl Oleate is stable under normal conditions, but can undergo a hydrolysis reaction with water to produce isopropanol and oleic acid.

Uses
Palmester 1412 Isopropyl Oleate also has good low temperature properties.
Palmester 1412 Isopropyl Oleate can effectively reduce the freezing point and cold filter point of biodiesel and improve the low temperature flow properties of biodiesel.

Synthesis and Characterization
Palmester 1412 Isopropyl Oleate can be synthesized by several methods, including esterification, transesterification, and direct esterification.
The most common method is esterification, where isopropyl alcohol and Palmester 1412 Isopropyl Oleate are reacted in the presence of a catalyst such as sulfuric acid.
The reaction results in the formation of isopropyl oleate and water.
The characterization of Palmester 1412 Isopropyl Oleate is done using various analytical methods.
These methods include infrared spectroscopy, gas chromatography, and nuclear magnetic resonance.
PALMESTER 1412 ISOPROPYL OLEATE

Palmester 1412 Isopropyl Oleate, a clear liquid, is an ester resulting from the combination of isopropyl alcohol and oleic acid.
With its smooth and non-greasy texture, Palmester 1412 Isopropyl Oleate serves as an excellent emollient in cosmetic formulations.
Palmester 1412 Isopropyl Oleate plays a key role as a skin-conditioning agent, contributing to the softness and hydration of the skin.

CAS Number: 112-11-8
EC Number: 203-935-4

Isopropyl Oleate, Oleic Acid Isopropyl Ester, Ester of Isopropyl Alcohol and Oleic Acid, Isopropyl Ester of Oleic Acid, Isopropyl Oleate Ester, Oleic Acid Ester with Isopropyl Alcohol, Isopropyl Oleate Estol 1511, Isopropyl Oleate Estol 1515, Isopropyl Oleate Estol 1618, Estol 1650 Isopropyl Oleate, Estol 1655 Isopropyl Oleate, Isopropyl Oleate Estol 1762, Isopropyl Oleate Estol 1862, Isopropyl Oleate Estol 1865, Isopropyl Oleate Estol 1868, Isopropyl Oleate Estol 1875, Isopropyl Oleate Estol 1895, Isopropyl Oleate Estol 1911, Isopropyl Oleate Estol 1915, Isopropyl Oleate Estol 1962, Isopropyl Oleate Estol 1965, Isopropyl Oleate Estol 1968, Isopropyl Oleate Estol 1975, Isopropyl Oleate Estol 1985, Isopropyl Oleate Estol 2011, Isopropyl Oleate Estol 2015, Isopropyl Oleate Estol 2062, Isopropyl Oleate Estol 2065, Isopropyl Oleate Estol 2068, Isopropyl Oleate Estol 2075, Isopropyl Oleate Estol 2085, Isopropyl Oleate Estol 3011, Isopropyl Oleate Estol 3015, Isopropyl Oleate Estol 3062, Isopropyl Oleate Estol 3065, Isopropyl Oleate Estol 3068, Isopropyl Oleate Estol 3075, Isopropyl Oleate Estol 3085, Isopropyl Oleate Estol 4011, Isopropyl Oleate Estol 4015, Isopropyl Oleate Estol 4062, Isopropyl Oleate Estol 4065, Isopropyl Oleate Estol 4068, Isopropyl Oleate Estol 4075, Isopropyl Oleate Estol 4085, Isopropyl Oleate Estol 5011, Isopropyl Oleate Estol 5015, Isopropyl Oleate Estol 5062, Isopropyl Oleate Estol 5065, Isopropyl Oleate Estol 5068, Isopropyl Oleate Estol 5075, Isopropyl Oleate Estol 5085, IPM Oleate, Oleate Ester of Isopropyl Alcohol, Oleic Acid Ester with 2-Propanol, 2-Propanol Oleate, 1-Methylethyl Ester of Oleic Acid, Oleic Acid Ester with Propan-2-ol, Isopropanol Oleate, Oleic Acid 2-Propanol Ester, Ester of Oleic Acid and Isopropanol, Oleic Acid Ester with Isopropanol.



APPLICATIONS


Palmester 1412 Isopropyl Oleate widespread application in skincare products, serving as a key emollient for lotions and creams.
Its role in cosmetic formulations extends to makeup products, contributing to the smooth application of foundations and concealers.
In the pharmaceutical industry, Palmester 1412 Isopropyl Oleate is utilized in topical formulations, enhancing the delivery of active ingredients.
Haircare products, including conditioners and styling formulations, benefit from Palmester 1412 Isopropyl Oleate's hair-conditioning properties.

Palmester 1412 Isopropyl Oleate's use as a lubricant base fluid is essential in automotive applications, ensuring efficient and smooth operation of mechanical components.
Palmester 1412 Isopropyl Oleate serves as a plasticizer in polymer formulations, influencing the flexibility and resilience of plastic materials.
Its presence in cleaning and maintenance products enhances the spreadability and performance of these formulations.

Palmester 1412 Isopropyl Oleate is a valuable ingredient in sunscreens, contributing to even application and improved skin feel.
Palmester 1412 Isopropyl Oleate is used in the production of personal lubricants, providing a smooth and non-irritating experience.
In the textile industry, Isopropyl Oleate is employed as a fabric softener, enhancing the feel of textiles.

Palmester 1412 Isopropyl Oleate is found in adhesive formulations, improving the adhesive properties and application of these products.
Palmester 1412 Isopropyl Oleate is used in the formulation of insect repellents, contributing to the spreadability of the repellent on the skin.

Its application in the manufacturing of candles enhances the texture and appearance of the candles.
Palmester 1412 Isopropyl Oleate plays a role in the production of bath oils and bath bombs, contributing to a luxurious bathing experience.
Palmester 1412 Isopropyl Oleate is incorporated into deodorant formulations, improving the glide and feel during application.
Palmester 1412 Isopropyl Oleate is utilized in the production of pet care products, including grooming formulations for pets.

Its use in the creation of massage oils enhances the glide and moisturizing properties of the oils.
Palmester 1412 Isopropyl Oleate is found in anti-aging creams, contributing to the overall texture and efficacy of these formulations.
Palmester 1412 Isopropyl Oleate is used in the production of industrial lubricants, ensuring the smooth operation of machinery.
Palmester 1412 Isopropyl Oleate is present in paint formulations, contributing to the spreadability and finish of the paint.

Palmester 1412 Isopropyl Oleate finds application in the formulation of leather treatments, improving the softness and conditioning of leather products.
Palmester 1412 Isopropyl Oleate is utilized in the production of hair dyes, improving the spreadability and application of the dye.
Palmester 1412 Isopropyl Oleate is found in the formulation of nail polishes, contributing to the smooth and even application of the polish.

Palmester 1412 Isopropyl Oleate is employed in the creation of cosmetic wipes, enhancing the effectiveness of these skincare products.
Its use in the production of industrial and household cleaners improves the spreadability and performance of these cleaning solutions.

Palmester 1412 Isopropyl Oleate is a common ingredient in facial serums, contributing to the delivery of active ingredients and promoting skin health.
Its inclusion in baby care products, such as baby oils and lotions, provides gentle and moisturizing properties for delicate baby skin.

Palmester 1412 Isopropyl Oleate is employed in the formulation of shaving creams and gels, ensuring a smooth and comfortable shaving experience.
In the production of hair serums, Isopropyl Oleate helps in enhancing the shine and manageability of the hair.
Palmester 1412 Isopropyl Oleate finds application in the creation of cuticle oils, contributing to the nourishment and maintenance of healthy cuticles.
Palmester 1412 Isopropyl Oleate is used in sunless tanning products, aiding in the even application and absorption of tanning agents.

Its presence in massage creams and lotions enhances the gliding effect during massages and provides skin-conditioning benefits.
Palmester 1412 Isopropyl Oleate is utilized in the manufacturing of lip glosses, contributing to their smooth and glossy texture on the lips.
Palmester 1412 Isopropyl Oleate plays a role in the formulation of intimate care products, including personal lubricants, due to its non-irritating properties.

Palmester 1412 Isopropyl Oleate is found in the production of perfumes, helping to disperse fragrance notes evenly on the skin.
Its use in eye makeup removers contributes to the effective and gentle removal of eye makeup products.
Palmester 1412 Isopropyl Oleate is present in the creation of dry shampoos, providing a non-greasy and refreshing option for hair cleansing.
Palmester 1412 Isopropyl Oleate finds application in the formulation of hand sanitizers, counteracting the drying effects of alcohol on the skin.

Palmester 1412 Isopropyl Oleate is used in the production of solid perfumes, ensuring a smooth and easily applicable consistency.
Its inclusion in natural and organic deodorants enhances the glide and comfort during application.

Isopropyl Oleate is utilized in the creation of eyebrow pencils and pomades, aiding in the smooth application and blending of color.
In the production of tattoo inks, Isopropyl Oleate may contribute to improved pigment dispersion and application.
Palmester 1412 Isopropyl Oleate is found in the formulation of hair masks, providing nourishment and revitalization to the hair.
Palmester 1412 Isopropyl Oleate is present in the creation of natural and organic mascaras, contributing to a clump-free and conditioning formula.

Its use in foot creams and scrubs enhances the moisturizing and softening effects on rough and dry skin.
Palmester 1412 Isopropyl Oleate finds application in the creation of acne treatment products, delivering active ingredients without causing excessive dryness.
Palmester 1412 Isopropyl Oleate is employed in the formulation of natural and organic foundations, improving the spreadability and blendability of pigments.

Palmester 1412 Isopropyl Oleate is used in the production of lip scrubs, aiding in exfoliation and smoothing of the lips.
Its presence in natural and organic night creams contributes to the skin-conditioning and rejuvenating effects.
Palmester 1412 Isopropyl Oleate is found in the formulation of makeup setting sprays, helping to set makeup without compromising its appearance.

Palmester 1412 Isopropyl Oleate is commonly used in the formulation of foundation primers, providing a smooth base for makeup application.
Its inclusion in natural and organic serums enhances the penetration of active ingredients for targeted skincare benefits.
Palmester 1412 Isopropyl Oleate is found in the production of natural and organic hair conditioners, improving hair texture and manageability.
Palmester 1412 Isopropyl Oleate plays a role in the creation of cuticle conditioners, aiding in the maintenance of healthy and hydrated cuticles.

Palmester 1412 Isopropyl Oleate is used in the manufacturing of bath salts, contributing to the dispersion of fragrance and moisturizing effects.
Its presence in foot scrubs and exfoliating products enhances the removal of dead skin cells, leaving feet soft and rejuvenated.

Palmester 1412 Isopropyl Oleate is utilized in the formulation of hair styling creams, providing hold and definition without stiffness.
In the production of anti-aging serums, Isopropyl Oleate contributes to the luxurious feel and absorption of active ingredients.
Palmester 1412 Isopropyl Oleate is found in natural and organic body lotions, imparting a non-greasy finish while moisturizing the skin.
Palmester 1412 Isopropyl Oleate is used in the creation of bath oils, creating a soothing and moisturizing experience during baths.

Its inclusion in natural and organic blushes contributes to a seamless and blendable application on the cheeks.
Palmester 1412 Isopropyl Oleate plays a role in the formulation of fragrance oils, aiding in the even diffusion of scents in various products.

Palmester 1412 Isopropyl Oleate is utilized in the production of natural and organic sunscreens, enhancing the spreadability and even coverage.
Palmester 1412 Isopropyl Oleate is found in the formulation of beard balms, providing conditioning benefits for facial hair and skin.
Its use in cuticle repair creams contributes to the healing and nourishment of damaged cuticles.
Palmester 1412 Isopropyl Oleate is employed in the creation of natural and organic hair mists, enhancing shine and manageability.

Palmester 1412 Isopropyl Oleate is present in natural and organic hand creams, providing quick absorption and long-lasting hydration.
In the formulation of natural and organic eye creams, Isopropyl Oleate contributes to smoother application and improved skin texture.
Palmester 1412 Isopropyl Oleate is used in the creation of lip gloss balms, combining hydration with a glossy finish.

Its presence in natural and organic body scrubs enhances the exfoliating and moisturizing effects on the skin.
Palmester 1412 Isopropyl Oleate plays a role in the production of cuticle butter, offering intensive conditioning for nails and cuticles.
Palmester 1412 Isopropyl Oleate is found in natural and organic body washes, contributing to a luxurious lather and skin-conditioning properties.

Palmester 1412 Isopropyl Oleate is utilized in the formulation of natural and organic facial cleansers, aiding in the removal of impurities.
Its inclusion in natural and organic hair masks enhances the nourishing and revitalizing effects on the hair.
Isopropyl Oleate is found in the production of natural and organic lip serums, providing hydration and a smooth feel.



DESCRIPTION


Palmester 1412 Isopropyl Oleate, a clear liquid, is an ester resulting from the combination of isopropyl alcohol and oleic acid.
With its smooth and non-greasy texture, Palmester 1412 Isopropyl Oleate serves as an excellent emollient in cosmetic formulations.
Palmester 1412 Isopropyl Oleate plays a key role as a skin-conditioning agent, contributing to the softness and hydration of the skin.

Palmester 1412 Isopropyl Oleate exhibits a high spreadability factor, making it valuable in skincare products for its easy application and absorption.
Derived from renewable sources, it aligns with sustainable practices, serving as a biodegradable fatty ester.

Its compatibility with various ingredients allows for a wide range of applications in cosmetics and personal care products.
As a lubricant base fluid, Palmester 1412 Isopropyl Oleate enhances the performance of formulations requiring smooth and efficient lubrication.

Palmester 1412 Isopropyl Oleate acts as a viscosity modifier, influencing the thickness and flow characteristics of the products it is incorporated into.
Palmester 1412 Isopropyl Oleate serves as a plasticizer for polymers, imparting flexibility and resilience to polymer-based formulations.
Suitable for both internal and external automotive applications, it finds utility in lubricating and conditioning automotive components.

Its presence in transportation, appliances, and electrical markets highlights its adaptability to diverse industrial applications.
Palmester 1412 Isopropyl Oleate's incorporation in household products and consumer goods enhances the sensory experience of these products.

Recommended for packaging materials, Palmester 1412 Isopropyl Oleate contributes to the overall performance and feel of packaging solutions.
Its application in pipes, hoses, and fittings emphasizes its role in ensuring smooth functionality and longevity in these components.

Palmester 1412 Isopropyl Oleate's use in wiring and cables showcases its compatibility with materials commonly used in electrical applications.
In building and construction, it contributes to the effectiveness of formulations for various construction-related products.
The KOSHER and HALAL certifications validate its suitability for products adhering to specific dietary requirements.

Palmester 1412 Isopropyl Oleate's role in Estol formulations underscores its use in specific product lines for diverse applications.
As a clear and colorless liquid, it maintains the aesthetic integrity of formulations in which it is included.
Palmester 1412 Isopropyl Oleate is known for its stability over time, contributing to the longevity and quality of cosmetic and industrial products.

Its presence in skincare formulations enhances the overall moisturizing and conditioning effects on the skin.
Palmester 1412 Isopropyl Oleate's biodegradability reflects a commitment to environmentally conscious practices in product development.
Palmester 1412 Isopropyl Oleate's use in automotive applications extends to both internal components and external finishes.

Palmester 1412 Isopropyl Oleate's versatility makes it a valuable ingredient in formulations targeting diverse industries and consumer needs.
Known for its ease of incorporation and effectiveness, Palmester 1412 Isopropyl Oleate continues to be a sought-after ingredient in the formulation of various cosmetic, industrial, and personal care products.



FIRST AID


Inhalation:

If inhaled, move the affected person to fresh air.
If breathing difficulties persist, seek medical attention.


Skin Contact:

In case of skin contact, remove contaminated clothing.
Wash the affected area with plenty of soap and water.
If irritation or redness occurs, seek medical advice.


Eye Contact:

In case of contact with eyes, rinse cautiously with water for several minutes, removing contact lenses if present.
Seek medical attention if irritation persists.


Ingestion:

If swallowed, do not induce vomiting unless directed by medical personnel.
Rinse mouth with water and seek immediate medical attention.


Firefighting Measures:

Extinguishing Media:

Use fire-extinguishing media suitable for surrounding materials (e.g., water spray, foam, dry chemical).


Special Firefighting Procedures:

Wear appropriate protective equipment.
Evacuate the area if the fire is uncontrollable.


Unusual Fire and Explosion Hazards:

No unusual fire or explosion hazards reported.


Accidental Release Measures:

Personal Precautions:

Wear appropriate protective equipment.
Avoid breathing vapors or dust.
Provide adequate ventilation.


Environmental Precautions:

Prevent the substance from entering sewers, watercourses, or low areas.


Clean-Up Methods:

Absorb spilled material with an inert absorbent.
Collect in a suitable container for disposal.


Notes to Physicians:

Treat symptomatically based on individual reactions.
Provide supportive care as necessary.



HANDLING AND STORAGE


Handling:

Handling Procedures:
Follow good industrial hygiene practices during handling.
Wash hands thoroughly after handling and before eating, drinking, or smoking.

Protection Against Fire and Explosion:
Take measures to prevent the buildup of electrostatic charges.
Use explosion-proof equipment if applicable.

Ventilation:
Ensure adequate ventilation in areas where the product is handled or processed.
Use local exhaust ventilation if necessary to control airborne concentrations.

Protective Measures:
Wear appropriate personal protective equipment (PPE), including gloves, safety goggles, and protective clothing.
Use respiratory protection if exposure limits are exceeded.

Storage Compatibility:
Store away from incompatible materials and substances.
Check the SDS for specific information on substances to avoid.

Handling Precautions:
Avoid contact with eyes, skin, and clothing.
Do not eat, drink, or smoke while handling the product.
Avoid inhalation of vapors or dust.


Storage:

Storage Conditions:
Store in a cool, dry, and well-ventilated area.
Keep away from heat sources, direct sunlight, and open flames.

Storage Temperature:
Store within a specified temperature range, as indicated in the SDS.

Storage Containers:
Use approved containers made of compatible materials.
Keep containers tightly closed when not in use to prevent contamination.

Incompatible Materials:
Store away from incompatible materials, as listed in the SDS.

Specific End Uses:
Store the product in a manner consistent with its intended applications.

Control Measures:
Implement engineering controls to minimize exposure during storage.
Use secondary containment to prevent spills from reaching the environment.

Handling of Leaked or Spilled Material:
Clean up spills immediately, following appropriate safety measures.
Dispose of waste in accordance with local regulations.

Storage Stability:
Check the product's stability over time and adhere to expiration dates if applicable.
PALMESTER 1417 ETHYLHEXYL OLEATE
Palmester 1417 Ethylhexyl Oleate made from our oleic acid and designed for use in a wide variety of applications where the properties of a high quality ester are required.
Palmester 1417 Ethylhexyl Oleate is intended for uses where excellent color, stability and odor characteristics and natural origin are desired.
Palmester 1417 Ethylhexyl Oleate finds application in personal care formulations as an emollient or in lubricants as a friction modifier in engine oils or as a feed for further modification.

CAS: 26399-02-0
MF: C26H50O2
MW: 394.67
EINECS: 247-655-0

Synonyms
2-ethylhexyl oleate;9-Octadecenoic acid (9Z)-, 2-ethylhexyl ester;2-Ethylhexyloleat;2-Ethylhexyl 9-octadecenoate;(Z)-9-Octadecenoic acid 2-ethylhexyl ester;Oleic acid 2-ethylhexyl ester;2-Ethyl hexyl Oleate(2EHS);2-ethylhexyloctadec-9-enoate;2-Ethylhexyl oleate;26399-02-0;ethylhexyl oleate;9-Octadecenoic acid (9Z)-, 2-ethylhexyl ester;2-ETHYLHEXYL (9Z)-OCTADEC-9-ENOATE;2-ethylhexyl (Z)-octadec-9-enoate;2-Ethylhexanol oleic acid ester;9-Octadecenoic acid (Z)-, 2-ethylhexyl ester;R34927QY59;UNII-R34927QY59;2-ethylhexyloleate;EINECS 247-655-0;SABODERM EO;SYMPATENS-EO;DUB OO;EC 247-655-0;AEC ETHYLHEXYL OLEATE;SCHEMBL333602;Oleic acid, 2-ethylhexyl ester;ETHYLHEXYL OLEATE [INCI;DTXSID90893468;(+/-)-ETHYLHEXYL OLEATE;BBA39902;2-ETHYLHEXYL 2-OCTADECENOATE;ETHYLHEXYL OLEATE, (+/-)-;AKOS027322108;AS-66491;NS00004020;2-OCTADECENOIC ACID, 2-ETHYLHEXYL ESTER;Q27287724

Palmester 1417 Ethylhexyl Oleate has been used as a viscocity control agent in personal care for products with high fat or wax contents, and for some other uses in lubricants and cosmetics such as bath oils, hair preparations and creams.
Palmester 1417 Ethylhexyl Oleate is a branched mono-saturated fatty acid ester obtained from 2-ethylhexanol and oleic fatty acid, mainly from palm oil.
Clear liquid at room temperatures with a melting point around -20 ºC.
Cosmetic formulations: Skin conditioning, emollient
Industrial uses: washing & cleaning products manufacturer, lubricants and greases, adhesives and sealants, polishes and waxes, textile treatment products and dyes and polymers.

Palmester 1417 Ethylhexyl Oleate is a chemical compound that belongs to the group of fatty esters.
Palmester 1417 Ethylhexyl Oleate is a liquid that is chemically stable and has a low surface tension.
Palmester 1417 Ethylhexyl Oleate has been shown to be an effective magnetic particle for water permeability, with a spacing of 0.2 nm and a viscosity of 20 cP.
Palmester 1417 Ethylhexyl Oleate can also act as a homogeneous catalyst in chemical reactions, such as the inhibition constant for fatty acid hydrolysis and the surface methodology for polymers.

2-ethylhexyl oleate Chemical Properties
Boiling point: 465.8±24.0 °C(Predicted)
density: 0.867±0.06 g/cm3(Predicted)
LogP: 11.429 (est)
CAS DataBase Reference: 26399-02-0
EPA Substance Registry System: Palmester 1417 Ethylhexyl Oleate (26399-02-0)
PALMESTER 1451 N-BUTYL STEARATE
Palmester 1451 n-Butyl Stearate is a fatty acid ester that is the butyl ester of stearic acid.
Palmester 1451 n-Butyl Stearate has a role as an algal metabolite.
Palmester 1451 n-Butyl Stearate derives from an octadecanoic acid.

CAS: 123-95-5
MF: C22H44O2
MW: 340.58
EINECS: 204-666-5

Synonyms
OCTADECANOIC ACID BUTYL ESTER;ButylStearateForSynthesis;N-BUTYL PALMITATE/-STEARATE;butyl stearate, tech.;FEMA 2214;BUTYL STEARATE;Butyl stearate Stearic acid butyl ester;BUTYL OCTADECANOATE;BUTYL STEARATE;123-95-5;N-Butyl stearate;Butyl octadecanoate;Octadecanoic acid, butyl ester;Kesscoflex BS;n-Butyl octadecanoate;Stearic acid, butyl ester;Butyl octadecylate;Kessco BSC;Wickenol 122;Witcizer 200;Witcizer 201;Starfol BS-100;Emerest 2325;Tegester butyl stearate;RC plasticizer B-17;Uniflex BYS;Groco 5810;APEX 4;FEMA No. 2214;Batyl stearate;Stearic acid butyl ester;NSC 4820;6Y0AI5605C;NSC-4820;Stearic Acid n-Butyl Ester;68154-28-9;BS;Wilmar butyl stearate;FEMA Number 2214;HSDB 942;Estrex 1B 54, 1B 55;EINECS 204-666-5;BRN 1792866;n-butylstearate;UNII-6Y0AI5605C;AI3-00398;Kessco BS;Unimate BYS;Uniflex BYS-tech;Oleo-Coll LP;C22H44O2;EINECS 268-908-1;Kemester 5510;Priolube 1451;Witconol 2326;Butyl stearate (NF);Radia 7051;Butyl stearate, ~99%;ADK STAB LS-8;Stearic acid-n-butyl ester;BUTYL STEARATE [II];BUTYL STEARATE [MI];SCHEMBL28437;BUTYL STEARATE [FCC];BUTYL STEARATE [FHFI];BUTYL STEARATE [INCI];BUTYL STEARATE [USP-RS];DTXSID5027013;N-BUTYL STEARATE [HSDB];CHEBI:85983;FEMA 2214;NSC4820;Butyl stearate, analytical standard;LMFA07010795;MFCD00026669;AKOS015901590;BS-14737;Butyl stearate, technical, 40-60% (GC);FT-0631720;NS00006400;S0077;D10681;D70203;J-005011;W-204214;Q10442124;Butyl stearate, United States Pharmacopeia (USP) Reference Standard

Palmester 1451 n-Butyl Stearate is a fatty acid ester, which has application in cosmetics, personal care products, and as an emollient in food industries.
Palmester 1451 n-Butyl Stearate is composed of n-butyl stearate.
Palmester 1451 n-Butyl Stearate can be used as a lubricant base fluid.
Palmester 1451 n-Butyl Stearate is a fatty ester derived from renewable vegetable oils.
Palmester 1451 n-Butyl Stearate acts as a lubricant, viscosity modifier, plasticizer for polymer.
Palmester 1451 n-Butyl Stearate is a biodegradable grade.
Used in internal & external automotive, transportation, appliances, electrical market, household products and consumer goods.
Palmester 1451 n-Butyl Stearate is also suitable for packaging, pipe, hoses & fittings, wiring & cables, building and construction.
Palmester 1451 n-Butyl Stearate is KOSHER and HALAL certified.
Palmester 1451 n-Butyl Stearate is a fatty acid ester that is the butyl ester of stearic acid.
Palmester 1451 n-Butyl Stearate has a role as an algal metabolite.
Palmester 1451 n-Butyl Stearate is functionally related to an octadecanoic acid.

Palmester 1451 n-Butyl Stearate Chemical Properties
Melting point: 17-22 °C
Boiling point: 220°C (25 mmHg)
Density: 0.861 g/mL at 20 °C(lit.)
Refractive index: n20/D 1.443
FEMA: 2214 | BUTYL STEARATE
Fp: 25 °C
Storage temp.: 2-8°C
Form: Liquid
Specific Gravity: 0.856
Color: White or Colorless to Light yellow
Odor: at 100.00 %. mild fatty oily
Odor Type: fatty
Water Solubility: Immiscible with water. Miscible with ethanol and acetone
FreezingPoint: 25.0 to 27.0 ℃
JECFA Number: 184
Merck: 14,1589
BRN: 1792866
Exposure limits: ACGIH: TWA 10 mg/m3; TWA 3 mg/m3
Dielectric constant: 3.1(30℃)
LogP: 9.70
CAS DataBase Reference: 123-95-5(CAS DataBase Reference)
NIST Chemistry Reference: Palmester 1451 n-Butyl Stearate 123-95-5)
EPA Substance Registry System: Palmester 1451 n-Butyl Stearate (123-95-5)

Palmester 1451 n-Butyl Stearate is a colorless or pale yellow oily liquid or low melting waxy solid.
Palmester 1451 n-Butyl Stearate has no odor or a faintly fatty odor.
soluble in acetone, chloroform, soluble in ethanol, insoluble in water.

Uses
Palmester 1451 n-Butyl Stearate is used as finishing agents, lubricants and lubricant additives.
Palmester 1451 n-Butyl Stearate is also used as a plasticizer, food packaging material and as a dye solvent.
Palmester 1451 n-Butyl Stearate acts as a reactant and involved in the preparation of octadecanoic acid methyl ester by reacting with methanol.
Palmester 1451 n-Butyl Stearate finds application as a binder in cosmetics like soaps, shampoos and shaving creams, skin conditioners and surfactants for cosmetic formulations.
Palmester 1451 n-Butyl Stearate is a stearic acid used in very small quantities in cosmetic preparations as an emulsifier for creams and lotions.
Palmester 1451 n-Butyl Stearate has been shown to cause allergic reactions.

Palmester 1451 n-Butyl Stearate is an internal lubricant for a variety of resin processing, non-toxic, waterproof and good thermal stability.
Palmester 1451 n-Butyl Stearate can also be used as a lubricant for fabrics, waterproofing agents, additives for lubricants, and base materials for cosmetics.
Suitable for PVC transparent products and pipes, used as internal lubricant for resin processing.

Preparation
Palmester 1451 n-Butyl Stearate is obtained by esterification of stearic acid and butanol, dealcoholization, washing with water and pressure filtration.
By reacting silver state with n-butyl iodide at 100°C by transesterification of glyceryl tristearate (tristearin) with n-butyl alcohol.
PALMESTER 1512 ISOPROPYL MYRISTATE
Palmester 1512 Isopropyl Myristate is odorless when pure.
Palmester 1512 Isopropyl Myristate may be synthesized by conventional esterification of isopropanol with myristic acid.
Palmester 1512 Isopropyl Myristate is a fatty acid ester.

CAS: 110-27-0
MF: C17H34O2
MW: 270.45
EINECS: 203-751-4

Synonyms
Isopropyl Myristate, 96% 25GR;IPM 100;IPM-EX;IPM-R;Radia 7730 (IPM);Isopropyl myristate Vetec(TM) reagent grade, 98%;MYRISTIC ACID ISOPROPYL ESTER MINIMU;ISO-PROPYL N-TETRADECANOATE;ISOPROPYL MYRISTATE;110-27-0;Isopropyl tetradecanoate;Estergel;Isomyst;Tetradecanoic acid, 1-methylethyl ester;Bisomel;Promyr;Deltyl Extra;Kesscomir;Tegester;Sinnoester MIP;Crodamol IPM;Plymoutm IPM;Starfol IPM;Unimate IPM;Kessco IPM;Stepan D-50;Emcol-IM;Wickenol 101;Emerest 2314;propan-2-yl tetradecanoate;1-Methylethyl tetradecanoate;Deltylextra;Myristic acid isopropyl ester;JA-FA IPM;Crodamol I.P.M.;Kessco isopropyl myristate;FEMA No. 3556;Tetradecanoic acid, isopropyl;Myristic acid, isopropyl ester;Tetradecanoic acid, isopropyl ester;Caswell No. 511E;HSDB 626;NSC 406280;Isopropyl myristate [USAN];1-Tridecanecarboxylic acid, isopropyl ester;UNII-0RE8K4LNJS;0RE8K4LNJS;EINECS 203-751-4;Estergel (TN);EPA Pesticide Chemical Code 000207;NSC-406280;BRN 1781127;methylethyl tetradecanoate;MFCD00008982;iso-Propyl N-tetradecanoate;DTXSID0026838;CHEBI:90027;EC 203-751-4;Tetradecanoic acid methyethyl ester;1405-98-7;NCGC00164071-01;WE(2:0(1Me)/14:0);MYRISTIC ACID, ISOPROPYL ALCOHOL ESTER;Isopropyl myristate, 98%;TETRADECONOIC ACID, 1-METHYLETHYL ESTER;DTXCID306838;ISOPROPYL MYRISTATE (II);ISOPROPYL MYRISTATE [II];ISOPROPYL MYRISTATE (MART.);ISOPROPYL MYRISTATE [MART.];ISOPROPYL MYRISTATE (USP-RS);ISOPROPYL MYRISTATE [USP-RS];CAS-110-27-0;ISOPROPYL MYRISTATE (EP MONOGRAPH);ISOPROPYL MYRISTATE [EP MONOGRAPH];IPM-EX;IPM-R;tetradecanoic acid 1-methylethyl ester;Deltyextra;Tegosoft M;Isopropyl myristate [USAN:NF];Liponate IPM;Crodamol 1PM;IPM 100;isopropyl-myristate;Lexol IPM;Isopropyltetradecanoate;Radia 7190;Isopropyl myristate (NF);Isopropyl tetradecanoic acid;SCHEMBL2442;Myristic acid-isopropyl ester;Isopropyl myristate, >=98%;CHEMBL207602;ISOPROPYL MYRISTATE [MI];WLN: 13VOY1&1;FEMA 3556;tetradecanoic acid isopropyl ester;ISOPROPYL MYRISTATE [FHFI];ISOPROPYL MYRISTATE [HSDB];ISOPROPYL MYRISTATE [INCI];ISOPROPYL MYRISTATE [VANDF];Isopropyl myristate, >=90% (GC);Tox21_112080;Tox21_202065;Tox21_303171;ISOPROPYL MYRISTATE [WHO-DD];LMFA07010677;NSC406280;s2428;AKOS015902296;Tox21_112080_1;DB13966;USEPA/OPP Pesticide Code: 000207;NCGC00164071-02;NCGC00164071-03;NCGC00256937-01;NCGC00259614-01;LS-14615;HY-124190;CS-0085813;FT-0629053;M0481;NS00006471;D02296;F71211;Isopropyl myristate; 1-Methylethyl tetradecanoate;EN300-25299830;Q416222;SR-01000944751;Isopropyl myristate, Vetec(TM) reagent grade, 98%;Q-201418;SR-01000944751-1;Isopropyl myristate, United States Pharmacopeia (USP) Reference Standard;TETRADECANOIC ACID,ISOPROPYL ESTER (MYRISTATE,ISOPROPYL ESTER);Isopropyl myristate, Pharmaceutical Secondary Standard; Certified Reference Material;InChI=1/C17H34O2/c1-4-5-6-7-8-9-10-11-12-13-14-15-17(18)19-16(2)3/h16H,4-15H2,1-3H

Palmester 1512 Isopropyl Myristate is an ester of isopropyl alcohol myristic acid.
Palmester 1512 Isopropyl Myristate is mainly used as a solubilizer, emulsifier and emollient in cosmetic and topical medicines.
Palmester 1512 Isopropyl Myristate also finds applications as a flavoring agent in the food industry.
Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
Palmester 1512 Isopropyl Myristate medical preparations to ameliorate the skin absorption.
Palmester 1512 Isopropyl Myristate has been largely studied and impulsed as a skin penetration enhancer.
At the moment the primary usage for which Palmester 1512 Isopropyl Myristate is formally indicated is as the active ingredient in a non-prescription pediculicide rinse.
Palmester 1512 Isopropyl Myristate is the ester of isopropyl alcohol and myristic acid.

Palmester 1512 Isopropyl Myristate is a nonsteroidal anti-inflammatory drug that is used to treat inflammatory conditions.
Palmester 1512 Isopropyl Myristate can be found in cosmetics, toiletries, and skin care products.
Palmester 1512 Isopropyl Myristate has been shown to inhibit the production of water vapor from skin cells and the development of allergic symptoms in vitro.
Palmester 1512 Isopropyl Myristate also has a role in preventing water loss from the skin by acting as a barrier to water vapor.
Palmester 1512 Isopropyl Myristate is also able to inhibit autoimmune diseases by inhibiting hiv infection in a model system.
Palmester 1512 Isopropyl Myristate has been shown to have antifungal properties and antimicrobial activity against Escherichia coli, Enterococcus faecalis, Pseudomonas aeruginosa, Staphylococcus aureus, Klebsiella pneumoniae, Proteus mirabilis, Bacillus cereus, Candida albicans and Aspergillus niger.
Isopropyl myrist
Palmester 1512 Isopropyl Myristate is colorless or light yellow oily liquid,can be dissolved with organic solvents,insoluble in water.
Palmester 1512 Isopropyl Myristate is the ester of isopropanol and myristic acid.
Palmester 1512 Isopropyl Myristate is one of the important additives of top grade cosmetics, and it owns excellent performance of infiltration, moistening and softening to skin, so it can be used as emulsifier and wetting agent of cosmetics.

Palmester 1512 Isopropyl Myristate Chemical Properties
Melting point: ~3 °C (lit.)
Boiling point: 193 °C/20 mmHg (lit.)
Density: 0.85 g/mL at 25 °C (lit.)
Vapor pressure: Vefractive index: n20/D 1.434(lit.)
FEMA: 3556 | ISOPROPYL MYRISTATE
Fp: >230 °F
Storage temp.: 2-8°C
Solubility: <0.05mg/l
Form: Liquid
Specific Gravity: 0.855 (20/4℃)
Color: Clear
Odor: odorless
Water Solubility: Miscible with alcohol. Immiscible with water and glycerol.
Merck: 14,5215
JECFA Number: 311
BRN: 1781127
Stability: Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey: AXISYYRBXTVTFY-UHFFFAOYSA-N
LogP: 7.71
CAS DataBase Reference: 110-27-0(CAS DataBase Reference)
NIST Chemistry Reference: Palmester 1512 Isopropyl Myristate (110-27-0)
EPA Substance Registry System: Palmester 1512 Isopropyl Myristate (110-27-0)

Palmester 1512 Isopropyl Myristate is a colorless and odorless liquid with a faint odor, and miscible with vegetable oil.
Palmester 1512 Isopropyl Myristate is not easy to be either hydrolyzed or become rancid.
The refractive index nD20 is 1.435~1.438, and the relative density (20°C) is 0.85~0.86.
Palmester 1512 Isopropyl Myristate is used in many applications, including pharma, food and personal care product manufacturing.
Palmester 1512 Isopropyl Myristate is virtually odorless, very slightly fatty, but not rancid
Palmester 1512 Isopropyl Myristate is a clear, colorless, practically odorless liquid of low viscosity that congeals at about 5°C.
Palmester 1512 Isopropyl Myristate consists of esters of propan-2-ol and saturated high molecular weight fatty acids, principally myristic acid.

Content Analysis
Weight 1.5 g sample. Then Palmester 1512 Isopropyl Myristate is determined by the method ester assay (OT-18).
The equivalent factor (e) in the calculation is 135.2.
Or Palmester 1512 Isopropyl Myristate is determined by a non-polar column method of gas chromatography (GT-10-4).

Uses
Palmester 1512 Isopropyl Myristate is a fatty acid ester which is used as solvent in water-in-oil emulsion, oils and fatty based ointments.
The use of Palmester 1512 Isopropyl Myristate is recommended in the Sterility Test chapter of the European, Japanese and United States Pharmacopoeia (EP, 2.6.13, JP, 4.06 and USP, 71) as diluent for oils and oily solutions, as well as for ointments and creams.
Indeed, its solvent properties improve the filterability of these samples.
Palmester 1512 Isopropyl Myristate is known as a penetration enhancer for topical preparations.
Palmester 1512 Isopropyl Myristate is a waterclear, low viscous oily liquid with a very good spreading capacity on the skin.
Palmester 1512 Isopropyl Myristate is mainly used in cosmetics as an oilcomponent for emulsions, bath oils and as a solvent for active substances.

Palmester 1512 Isopropyl Myristate is an emollient in cosmetic and pharmaceutical bases.
Palmester 1512 Isopropyl Myristate is an emollient, moisturizer, binder, and skin softener that also assists in product penetration.
An ester of myristic acid, Palmester 1512 Isopropyl Myristate is naturally occurring in coconut oil and nutmeg.
Although Palmester 1512 Isopropyl Myristate is generally considered comedogenic, some ingredient manufacturers clearly specify non-comedogenicity on their data sheets.
In cosmetic and topical medicinal Preparations where good absorption through the skin is desired. A jellied Palmester 1512 Isopropyl Myristate was marketed as Estergel.

Palmester 1512 Isopropyl Myristate is a polar emollient and is used in cosmetic and topical pharmaceutical preparations where skin absorption is desired.
Palmester 1512 Isopropyl Myristate is also used as a treatment for head lice.
Palmester 1512 Isopropyl Myristate is also in flea and tick killing products for pets.
Palmester 1512 Isopropyl Myristate is used to remove bacteria from the oral cavity as the non-aqueous component of the two-phase mouthwash product "Dentyl pH".
Palmester 1512 Isopropyl Myristate is also used as a solvent in perfume materials, and in the removal process of prosthetic make-up.
Hydrolysis of the ester from Palmester 1512 Isopropyl Myristate can liberate the acid and the alcohol.
The acid is theorized to be responsible for decreasing of the pH value of formulations.

Palmester 1512 Isopropyl Myristate is used in cosmetic and topical medicinal preparations where good absorption through the skin is desired.
Palmester 1512 Isopropyl Myristate is also used as a pesticide-free treatment against head lice which works by dissolving the wax that covers the exoskeleton of head lice, killing them by dehydration.
Palmester 1512 Isopropyl Myristate is used as a solvent in perfume materials.
Palmester 1512 Isopropyl Myristate is the non-aqueous component of the two-phase mouthwash, Dentyl pH, where it removes bacteria from the oral cavity.
Palmester 1512 Isopropyl Myristate is also used in the removal process of prosthetic make-up.
Palmester 1512 Isopropyl Myristate is also used in flea and tick products for pets.

Pharmaceutical Applications
Palmester 1512 Isopropyl Myristate is a nongreasy emollient that is absorbed readily by the skin.
Palmester 1512 Isopropyl Myristate is used as a component of semisolid bases and as a solvent for many substances applied topically.
Applications in topical pharmaceutical and cosmetic formulations include bath oils; make-up; hair and nail care products; creams; lotions; lip products; shaving products; skin lubricants; deodorants; otic suspensions; and vaginal creams.
For example, isopropyl myristate is a self-emulsifying component of a proposed cold cream formula, which is suitable for use as a vehicle for drugs or dermatological actives; Palmester 1512 Isopropyl Myristate is also used cosmetically in stable mixtures of water and glycerol.

Palmester 1512 Isopropyl Myristate is used as a penetration enhancer for transdermal formulations, and has been used in conjunction with therapeutic ultrasound and iontophoresis.
Palmester 1512 Isopropyl Myristate has been used in a water-oil gel prolonged-release emulsion and in various microemulsions.
Such microemulsions may increase bioavailability in topical and transdermal applications.
Palmester 1512 Isopropyl Myristate has also been used in microspheres, and significantly increased the release of drug from etoposide-loaded microspheres.
Palmester 1512 Isopropyl Myristate is used in soft adhesives for pressuresensitive adhesive tapes.

Pharmacology
Palmester 1512 Isopropyl Myristate is used in pharmaceutical preparations because it improves solubility and increases absorption through the skin.
External uses include a non-irritating iodine preparation for disinfecting the skin and aerosol bactericidal preparations for feminine hygiene use without irritation of the skin and mucous membranes.
Preparations for internal use include oral steroid formulations and anaesthetic injection solutions.
Veterinary medications containing Palmester 1512 Isopropyl Myristate include oral or parenteral compositions for lungworm infections and a spray formulation for bovine udders to treat mastitis, combat infection and improve the general skin condition.

Palmester 1512 Isopropyl Myristate has been found to be an effective repository vehicle for im injection of penicillin in rabbits and for sc administration of oestrogens in ovariectomized rats.
In assays on human forearms, vasoconstrictor activity of ointment preparations containing 0025% betamethasone 17-benzoate in white soft paraffin was increased by the presence of isopropyl myristate.
Donovan, Ohmart & Stoklosa noted that the good solvent properties of isopropyl myristate might increase the therapeutic activity of formulations by the apparent alteration in particle size of the active ingredients, so that further evaluation and clinical study would be necessary before its use in extemporaneous compounding could be recommended.
Studies in which the antifungal activity of paraben esters solubilized by surfactants was decreased by Palmester 1512 Isopropyl Myristate indicate that the effectiveness of medicinal substances may be influenced by the presence of surfactants and oily ingredients such as Palmester 1512 Isopropyl Myristate.

Production Method
Palmester 1512 Isopropyl Myristate is a product of esterification of myristic acid derived from re-steamed coconut coil with isopropyl alcohol.
(1) 200 kg myristic acid and 450 kg isopropyl alcohol were added into the reaction vessel in turn. After mixing, 360 kg sulfuric acid (98%) was added.
The reaction mixture was heated to reflux for 10 hours.
Isopropyl alcohol was then recovered, washed with ice water, and neutralized with Na2CO3 aqueous solution (10%).
Under normal pressure, isopropyl alcohol and water were distilled.
While under reduced pressure, Palmester 1512 Isopropyl Myristate was distilled (185°C/1.0kPa~195°C/2.7kPa).

(2) 90 kg isopropyl alcohol was added into the reaction vessel and then sulfuric acid as catalyst, with 5% of the total amount, was added.
During mixing, 228 kg myristic acid was added slowly.
The mixture was heated to reflux and water was continuously separated.
Until no water was separated, the reaction temperature was reduced and probe was obtained to measure the acid value.
When the acid value reached 1.5 mg KOH/g, the reaction was completed.
Alkali was then added for neutralization.
After the removal of water under reduced pressure, the pressure was further reduced for dealcoholization until the acid value was 0.05~1.0 mg KOH/g.
The final product is then Palmester 1512 Isopropyl Myristate.

Production Methods
Palmester 1512 Isopropyl Myristate may be prepared either by the esterification of myristic acid with propan-2-ol or by the reaction of myristoyl chloride and propan-2-ol with the aid of a suitable dehydrochlorinating agent.
A high-purity material is also commercially available, produced by enzymatic esterification at low temperature.

Biochem/physiol Actions
Palmester 1512 Isopropyl Myristate is used to change the physicochemical characteristics of microsheres such as poly(lactic-co-glycolic acid) (PLGA) microspheres.
Palmester 1512 Isopropyl Myristate is used as a oil phase component in the formulaton of microemulsion systems.

Side effects
Thrapecylate myristate is a medicine used to treat head lice infestations in adults and children 4 years of age and older.
Common side effects include skin irritation, rash, and contact dermatitis.
PALMESTER 1517 ISOPROPYL PALMITATE
Palmester 1517 Isopropyl Palmitate is a fatty acid ester obtained by the formal condensation of carboxy group of palmitic acid with propan-2-ol.
Metabolite observed in cancer metabolism.
Palmester 1517 Isopropyl Palmitate has a role as a human metabolite.

CAS: 142-91-6
MF: C19H38O2
MW: 298.5
EINECS: 205-571-1

Synonyms
kesscoipp;kesscoisopropylpalmitate;Lexol IPP;Liponate IPP;nikkolipp;Palmitic acid esters;Plymouth ipp;plymouthipp;ISOPROPYL PALMITATE;142-91-6;Isopropyl hexadecanoate;Hexadecanoic acid, 1-methylethyl ester;Isopalm;Wickenol 111;Deltyl;Isopal;Propal;Deltyl prime;Emerest 2316;Tegester isopalm;Ja-fa ippkessco;Sinnoester PIT;Crodamol IPP;Plymouth IPP;Starfol IPP;Unimate IPP;Kessco IPP;Emcol-IP;Isopropyl n-hexadecanoate;Nikkol IPP;Stepan D-70;Palmitic acid, isopropyl ester;Estol 103;Usaf ke-5;JA-FA Ipp;1-Methylethyl hexadecanoate;Kessco isopropyl palmitate;Hexadecanoic acid,isopropyl ester;Hariol ipp;propan-2-yl hexadecanoate;Palmitic Acid Isopropyl Ester;NSC 69169;Estol 1517;HSDB 2647;Tegosoft P;Liponate IPP;UNII-8CRQ2TH63M;EINECS 205-571-1;Lexol IPP;8CRQ2TH63M;NSC-69169;BRN 1786567;CHEBI:84262;2-propyl hexadecanoate;AI3-05733;Isopropyl palmitate (NF);Isopropyl palmitate [NF];MFCD00008993;DTXSID9027104;EC 205-571-1;4-02-00-01167 (Beilstein Handbook Reference);Isopropyl ester of hexadecanoic acid;NCGC00164128-01;WE(2:0(1Me)/16:0);DTXCID507104;ISOPROPYL PALMITATE (II);ISOPROPYL PALMITATE [II];ISOPROPYL PALMITATE (MART.);ISOPROPYL PALMITATE [MART.];ISOPROPYL PALMITATE (USP-RS);ISOPROPYL PALMITATE [USP-RS];ISOPROPYL PALMITATE (EP IMPURITY);ISOPROPYL PALMITATE [EP IMPURITY];CAS-142-91-6;ISOPROPYL PALMITATE (EP MONOGRAPH);ISOPROPYL PALMITATE [EP MONOGRAPH];iso-propylpalmitate;isopropyl-palmitate;Hexadecanoic acid 1-methylethyl ester;Radia 7200;1-methylethyl hexandecanoate;SCHEMBL7743;Palmitic acid-isopropyl ester;Isopropyl palmitate, >=90%;CHEMBL139055;Hexadecanoic acid isopropyl ester;Hexadecanoic acid, 1-methyl ester;ISOPROPYL PALMITATE [HSDB];ISOPROPYL PALMITATE [INCI];WLN: 15VOY1 & 1;ISOPROPYL PALMITATE [VANDF];NSC69169;Tox21_112085;Tox21_202558;ISOPROPYL PALMITATE [WHO-DD];LMFA07010675;AKOS015902011;Tox21_112085_1;CS-W012142;HY-W011426;NCGC00164128-02;NCGC00260107-01;BS-15396;Hexadecanoic acidisopropyl n-hexadecanoate;Isopropyl palmitate, technical grade, 90%;FT-0631830;NS00009869;P0005;1-Methylethyl ester1-methylethyl hexandecanoate;D04632;A885074;SR-01000944752;J-007718;Q2631777;SR-01000944752-1;Isopropyl hexadecanoate, European Pharmacopoeia (EP) Reference Standard;Isopropyl palmitate, United States Pharmacopeia (USP) Reference Standard;Isopropyl palmitate, Pharmaceutical Secondary Standard; Certified Reference Material

Palmester 1517 Isopropyl Palmitate is a fatty acid ester and an isopropyl ester.
Palmester 1517 Isopropyl Palmitate is functionally related to a hexadecanoic acid.
Palmester 1517 Isopropyl Palmitate is an analog of isopropyl myristate and an aliphatic ester used as a flavoring ingredient in food industry.
Palmester 1517 Isopropyl Palmitate is one of the volatile compounds found in Psidium salutare fruits and boiled buckwheat flour.
Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

Palmester 1517 Isopropyl Palmitate is a fatty acid ester obtained by the formal condensation of carboxy group of palmitic acid with propan-2-ol.
Metabolite observed in cancer metabolism.
Palmester 1517 Isopropyl Palmitate has a role as a human metabolite.
Palmester 1517 Isopropyl Palmitate is a fatty acid ester and an isopropyl ester.
Palmester 1517 Isopropyl Palmitate is functionally related to a hexadecanoic acid.
Palmester 1517 Isopropyl Palmitate is a reactive lipid that is used as a co-solvent in wastewater treatment.
Palmester 1517 Isopropyl Palmitate is also used to make dimethyl fumarate, an active ingredient for the treatment of alopecia areata.
Palmester 1517 Isopropyl Palmitate has been shown to be a good reactant in the kinetic study of particle formation.

The reaction mechanism of this lipid is not well understood, but Palmester 1517 Isopropyl Palmitate has been shown to have clinical relevance and clinical properties in vivo.
Palmester 1517 Isopropyl Palmitate is the ester of isopropyl alcohol and palmitic acid.
Palmester 1517 Isopropyl Palmitate is an emollient, moisturizer, thickening agent, and anti-static agent.
The chemical formula is CH3(CH2)14COOCH(CH3)2.
Palmester 1517 Isopropyl Palmitate is a texture enhancer and emollient as used in cosmetics.
Palmester 1517 Isopropyl Palmitate can potentially be problematic for those with oily skin, depending on the amount in the product and your skin’s response.
Palmester 1517 Isopropyl Palmitate may be synthetic or derived from plant and animal sources.

Palmester 1517 Isopropyl Palmitate Chemical Properties
Melting point: 11-13 °C (lit.)
Boiling point: 160°C 2mm
Density: 0.852 g/mL at 25 °C (lit.)
Vapor pressure: 0.007Pa at 25℃
Refractive index: n20/D 1.438(lit.)
Fp: >230 °F
Storage temp.: 2-8°C
Solubility: <0.001g/l
Color: Colourless
Odor: very sl. odor
Water Solubility: Not miscible or difficult to mix with water.
BRN: 1786567
InChIKey: XUGNVMKQXJXZCD-UHFFFAOYSA-N
LogP: 8.16
CAS DataBase Reference: 142-91-6(CAS DataBase Reference)
NIST Chemistry Reference: Palmester 1517 Isopropyl Palmitate(142-91-6)
EPA Substance Registry System: Palmester 1517 Isopropyl Palmitate (142-91-6)

Palmester 1517 Isopropyl Palmitate is a clear, colorless to pale yellow-colored, practically odorless viscous liquid that solidifies at less than 16°C.

Uses
Palmester 1517 Isopropyl Palmitate is an emollient and moisturizer, it also acts as a binder and solvent.
Similar to isopropyl myristate, Palmester 1517 Isopropyl Palmitate is produced from the combination of palmitic acid (coconut or palm oil) and isopropyl alcohol.
Enzymes are able to metabolize this ingredient and studies do not show allergic reactions or toxicity.
Some sources indicate comedogenicity potential.
Palmester 1517 Isopropyl Palmitate is used to formulate and evaluate the suitability of pluronic lecithin organogels containing flurbiprofen for topical application and to characterize microemulsion systems of isopropyl palmitate, water and 2:1 Brij 97, and 1-butanol by different experimental techniques.

Palmester 1517 Isopropyl Palmitate is an analogue of isopropyl myristate and a volatile aliphatic ester used in the food industry as a flavoring agent.
Palmester 1517 Isopropyl Palmitate is also used as a lubricant in the textile industry.
Palmester 1517 Isopropyl Palmitate is also used in cosmetics as an antistatic agent, binding agent, emollient, solvent and skin care agent.
At higher concentrations a comedogenic effect is possible.

Pharmaceutical Applications
Palmester 1517 Isopropyl Palmitate is a nongreasy emollient with good spreading characteristics, used in topical pharmaceutical formulations and cosmetics such as: bath oils; creams; lotions; make-up; hair care products; deodorants; lip products; suntan preparations; and pressed powders.
Palmester 1517 Isopropyl Palmitate is an established penetration enhancer for transdermal systems.
Palmester 1517 Isopropyl Palmitate has also been used in controlled-release percutaneous films.
Table I: Uses of isopropyl palmitate

Production Methods
Palmester 1517 Isopropyl Palmitate is prepared by the reaction of palmitic acid with propan-2-ol in the presence of an acid catalyst.
A high-purity material is also commercially available, which is produced by enzymatic esterification at low temperatures.

Side effects
Side effects for the skin: If overused, Palmester 1517 Isopropyl Palmitate may cause acne, blackheads, whiteheads, and clogged pores.
Depending on the content of the ingredients in the product, the skin may experience some irritation.
If Palmester 1517 Isopropyl Palmitate is used without dilution, it may cause comedoles.
People with oily skin should also avoid isopropyl palmitate.
Side effects for hair: Excessive use of products containing Palmester 1517 Isopropyl Palmitate on hair can make hair look untidy, oily, and untidy due to excessive moisture in the hair.
When there is an open wound on the scalp, Palmester 1517 Isopropyl Palmitate should also be avoided.
PALMESTER 1543 ETHYLHEXYL PALMITATE

Palmester 1543 Ethylhexyl Palmitate, also known as EHP, is a synthetic ester derived from renewable vegetable oils.
Palmester 1543 Ethylhexyl Palmitate serves as an emollient and fragrance enhancer in cosmetic formulations.
Palmester 1543 Ethylhexyl Palmitate is a colorless and odorless compound, meeting stringent standards for fragrance use.

CAS Number: 29806-73-3
EC Number: 249-862-1

Octyl Palmitate, EHP, Octyl Hexyl Ester, 2-Ethylhexyl Palmitate, Octyl Palmitate Ester, Palmester 1543, Hexyl Ester of Palmitic Acid, Ethylhexyl Ester of Palmitic Acid, Octyl Hexyl Palmitate, Ethylhexyl Palmitate Ester, Octyl Hexyl Palmitate Ester, Palmester 1543 EHP, Octyl Ester of Hexyl Palmitate, Ethylhexyl Ester Hexyl Palmitate, Palmitic Acid Ethylhexyl Ester, Octyl Palmitate Compound, Hexyl Ester of Ethylhexyl Palmitate, Octyl Palmitate Derivative, Ester of Ethylhexyl Palmitate, Ethylhexyl Palmitate Octyl Ester, Hexyl Palmitate Ethylhexyl Ester, Octyl Palmitate Hexyl Ester, Ethylhexyl Palmitate Palmester 1543, Palmitate 1543 Ester, Hexyl Ester of Octyl Palmitate, Ethylhexyl Ester of Octyl Palmitate, Octyl Ester of Ethylhexyl Palmitate, Palmitic Acid Hexyl Ester, EHP Palmester 1543, Octyl Palmitate Hexyl Ester Compound, Ethylhexyl Ester Octyl Palmitate, Palmester 1543 Octyl Palmitate, Octyl Ester of Palmitic Acid, Octyl Palmitate Ethylhexyl Ester, Hexyl Ester of Octyl Palmitate, Ethylhexyl Palmitate Hexyl Ester, Palmitate 1543 Octyl Hexyl Ester, Octyl Hexyl Ester of Ethylhexyl Palmitate, Octyl Palmitate Hexyl Ester Derivative, Ethylhexyl Ester of Hexyl Palmitate, Palmester 1543 Octyl Ester, Hexyl Palmitate Octyl Ester Compound, Octyl Palmitate Hexyl Ester Derivative, Ethylhexyl Palmitate Octyl Hexyl Ester, Octyl Ester of Hexyl Palmitate, Palmester 1543 Ethylhexyl Palmitate Ester, Hexyl Palmitate Octyl Ester Compound, Octyl Palmitate Hexyl Ester Palmester 1543, Ethylhexyl Palmitate Octyl Ester Compound, Hexyl Ester of Octyl Palmitate Ethylhexyl, Octyl Palmitate Hexyl Ester Ethylhexyl, Palmester 1543 Octyl Palmitate Hexyl Ester, Octyl Ester of Ethylhexyl Palmitate, Hexyl Palmitate Ethylhexyl Ester Compound, Octyl Palmitate Ethylhexyl Ester Palmester 1543, Hexyl Ester of Octyl Palmitate Ethylhexyl, Octyl Palmitate Hexyl Ester Ethylhexyl, Palmester 1543 Octyl Ester Hexyl Palmitate.



APPLICATIONS


Palmester 1543 Ethylhexyl Palmitate is commonly used as an emollient in various skincare products.
Palmester 1543 Ethylhexyl Palmitate is a key ingredient in night creams, providing moisturization and improving skin texture.

Hand creams often incorporate Palmester 1543 Ethylhexyl Palmitate for its skin-conditioning properties.
Palmester 1543 Ethylhexyl Palmitate is found in cleansing lotions, contributing to a smooth and gentle cleansing experience.

Baby creams utilize Palmester 1543 Ethylhexyl Palmitate for its emollient nature, suitable for delicate skin.
Massage lotions benefit from its glide-enhancing characteristics, making the application smoother.
Skincare formulations such as lotions and creams often feature Palmester 1543 Ethylhexyl Palmitate for a luxurious feel.

Palmester 1543 Ethylhexyl Palmitate is included in cosmetic products to enhance fragrance and olfactory experiences.
Palmester 1543 Ethylhexyl Palmitate serves as a replacement for mineral oil in skincare formulations.

Palmester 1543 Ethylhexyl Palmitate is used in formulations where the stability and keeping qualities of the product are crucial.
Cosmetic products designed for sensitive skin may include Palmester 1543 Ethylhexyl Palmitate for its gentle nature.
Sunscreen formulations may use this compound to improve the spreadability and skin-feel.
Palmester 1543 Ethylhexyl Palmitate is incorporated into makeup products like foundations for a smoother application.

Anti-aging creams often contain Palmester 1543 Ethylhexyl Palmitate to help moisturize and condition mature skin.
Lip balms may include Palmester 1543 Ethylhexyl Palmitate to provide a soft and moisturizing texture.

Palmester 1543 Ethylhexyl Palmitate is used in body lotions and creams to impart a silky and non-greasy feel on the skin.
Palmester 1543 Ethylhexyl Palmitate is a versatile ingredient in formulations for dry and chapped skin.
Hair care products, such as leave-in conditioners, may utilize this compound for its conditioning properties.

Palmester 1543 Ethylhexyl Palmitate is suitable for use in various cosmetic care products due to its broad applications.
Palmester 1543 Ethylhexyl Palmitate is found in skincare products targeting specific skin concerns, like hydration.
Cosmetics designed for a relaxing experience, such as massage creams, may contain this ester.
Palmester 1543 Ethylhexyl Palmitate is employed in formulations where a lightweight and easily spreadable texture is desired.

Palmester 1543 Ethylhexyl Palmitate can be part of the ingredients in moisturizing body washes and shower gels.
Palmester 1543 Ethylhexyl Palmitate is used in formulations where the focus is on providing a pleasant sensory experience.
Palmester 1543 Ethylhexyl Palmitate's versatility makes it a valuable ingredient in a wide range of cosmetic and personal care applications.

Palmester 1543 Ethylhexyl Palmitate is commonly included in formulations for facial moisturizers to provide a lightweight and non-greasy feel.
Its compatibility with various active ingredients makes it a versatile component in anti-acne creams and treatments.
Palmester 1543 Ethylhexyl Palmitate is often present in sunscreen lotions, contributing to an even application and improved skin feel.

Palmester 1543 Ethylhexyl Palmitate is utilized in foundation formulations to create a smooth and blendable texture.
Eye creams may incorporate Palmester 1543 Ethylhexyl Palmitate for its emollient properties to hydrate the delicate skin around the eyes.

BB creams and tinted moisturizers may contain this ester for its ability to enhance product spreadability.
Palmester 1543 Ethylhexyl Palmitate is added to makeup primers to create a smooth canvas for subsequent makeup application.
Palmester 1543 Ethylhexyl Palmitate finds application in lip glosses and lipsticks to provide a creamy and moisturizing consistency.
Palmester 1543 Ethylhexyl Palmitate is used in hand sanitizers and antibacterial gels to improve the texture of the product on the skin.

Palmester 1543 Ethylhexyl Palmitate is included in cuticle creams and nail care products for its skin-conditioning effects.
Palmester 1543 Ethylhexyl Palmitate is a common ingredient in after-shave lotions, offering soothing and moisturizing properties.
Palmester 1543 Ethylhexyl Palmitate is found in foot creams to help soften and hydrate dry and rough skin.
Palmester 1543 Ethylhexyl Palmitate is used in formulations for body scrubs and exfoliating products to enhance the overall skin-feel.

Palmester 1543 Ethylhexyl Palmitate contributes to the luxurious texture of body oils and massage oils.
Palmester 1543 Ethylhexyl Palmitate is often present in sunless tanning products for its skin-conditioning benefits.
Palmester 1543 Ethylhexyl Palmitate is utilized in deodorant formulations to improve the glide and spreadability.

Palmester 1543 Ethylhexyl Palmitate can be found in depilatory creams to enhance the smoothness of the product during application.
Palmester 1543 Ethylhexyl Palmitate is used in shaving creams and foams to provide a lubricating and moisturizing effect.
Palmester 1543 Ethylhexyl Palmitate is present in cosmetic wipes and towelettes for its emollient and skin-conditioning properties.

Palmester 1543 Ethylhexyl Palmitate may be incorporated into dry shampoo formulations for its hair-conditioning benefits.
Palmester 1543 Ethylhexyl Palmitate is a common ingredient in body powders, contributing to a silky and soft texture.
Palmester 1543 Ethylhexyl Palmitate is used in skincare serums and treatments to enhance the overall product experience.

Palmester 1543 Ethylhexyl Palmitate finds application in cosmetic formulations designed for sensitive or reactive skin.
Palmester 1543 Ethylhexyl Palmitate is included in cosmetic products for men, such as beard oils and grooming products.
Palmester 1543 Ethylhexyl Palmitate can be part of the formulation for bath oils and bath bombs, providing a luxurious bathing experience.

Palmester 1543 Ethylhexyl Palmitate is often included in body lotions and creams to impart a soft and velvety feel to the skin.
Palmester 1543 Ethylhexyl Palmitate is used in facial cleansers and makeup removers to enhance the effectiveness of the product while maintaining a pleasant texture.
Palmester 1543 Ethylhexyl Palmitate is employed in hand serums and treatments to nourish and hydrate the skin, especially targeting dry cuticles.
Palmester 1543 Ethylhexyl Palmitate is found in pre-makeup primers, helping create a smooth base for foundation application.

Palmester 1543 Ethylhexyl Palmitate is utilized in cosmetic formulations for individuals with oily or acne-prone skin due to its lightweight nature.
Palmester 1543 Ethylhexyl Palmitate is included in exfoliating scrubs, aiding in the removal of dead skin cells while providing a silky feel.

Palmester 1543 Ethylhexyl Palmitate is commonly added to tinted moisturizers to improve the spreadability of pigments on the skin.
Palmester 1543 Ethylhexyl Palmitate is used in intimate care products, such as personal lubricants, for its skin-friendly and emollient properties.
Palmester 1543 Ethylhexyl Palmitate is found in cuticle oils to soften and moisturize the cuticle area, promoting healthy nails.

Palmester 1543 Ethylhexyl Palmitate may be present in bath foams and shower gels, contributing to a luxurious bathing experience.
Palmester 1543 Ethylhexyl Palmitate is included in under-eye creams and serums to provide a smooth application and enhance hydration.

Palmester 1543 Ethylhexyl Palmitate is employed in cosmetic stick formulations, like solid perfumes, for its solidifying and skin-conditioning qualities.
Palmester 1543 Ethylhexyl Palmitate is utilized in body mists and sprays to enhance the even distribution of fragrance on the skin.
Palmester 1543 Ethylhexyl Palmitate is commonly found in cosmetic formulations targeting specific skin concerns, such as dry patches or rough areas.

Palmester 1543 Ethylhexyl Palmitate is present in foot sprays and powders to improve the application and comfort of the product.
Palmester 1543 Ethylhexyl Palmitate is used in cuticle balms and treatments to soften and moisturize the skin around the nails.
Palmester 1543 Ethylhexyl Palmitate can be found in cosmetic products designed for use during and after pregnancy to address skin changes.

Palmester 1543 Ethylhexyl Palmitate is included in facial masks, contributing to the product's texture and skin-conditioning properties.
Palmester 1543 Ethylhexyl Palmitate is employed in cosmetic formulations for men's grooming products, such as beard balms and beard oils.
Palmester 1543 Ethylhexyl Palmitate may be added to deodorant creams for its skin-friendly and emollient effects.

Palmester 1543 Ethylhexyl Palmitate is utilized in lip care products, including lip balms and treatments, for its moisturizing and smoothing properties.
Palmester 1543 Ethylhexyl Palmitate is found in cosmetic formulations for mature skin, providing anti-aging benefits and hydration.
Palmester 1543 Ethylhexyl Palmitate is commonly included in cosmetic formulations for individuals with sensitive or reactive skin.

Palmester 1543 Ethylhexyl Palmitate is used in sun care products beyond sunscreen formulations, contributing to the overall skin feel.
Palmester 1543 Ethylhexyl Palmitate is present in facial serums and treatments, enhancing the spreadability and absorption of active ingredients.



DESCRIPTION


Palmester 1543 Ethylhexyl Palmitate, also known as EHP, is a synthetic ester derived from renewable vegetable oils.
Palmester 1543 Ethylhexyl Palmitate serves as an emollient and fragrance enhancer in cosmetic formulations.
Palmester 1543 Ethylhexyl Palmitate is a colorless and odorless compound, meeting stringent standards for fragrance use.

Palmester 1543 Ethylhexyl Palmitate exhibits excellent keeping qualities, making it a desirable ingredient in skincare products.
Palmester 1543 Ethylhexyl Palmitate is readily biodegradable, contributing to environmentally friendly formulations.
Palmester 1543 Ethylhexyl Palmitate is a GMO-free alternative, emphasizing its commitment to natural and sustainable sourcing.

Palmester 1543 Ethylhexyl Palmitate is produced to high standards, ensuring consistency in both color and odor for cosmetic applications.
Palmester 1543 Ethylhexyl Palmitate is a safe and effective replacement for mineral oil in various skincare formulations.

BSE/TSE-free certification assures consumers that it is free from transmissible spongiform encephalopathy.
Its versatility allows for use in a variety of cosmetic care products, including night creams and hand creams.
Palmester 1543 Ethylhexyl Palmitate is a popular choice in cleansing lotions, offering a smooth and luxurious feel on the skin.

Baby creams often incorporate Palmester 1543 Ethylhexyl Palmitate for its gentle and emollient properties.
Massage lotions benefit from its skin-conditioning characteristics, enhancing the overall sensory experience.
Palmester 1543 Ethylhexyl Palmitate is HALAL certified, meeting dietary requirements for specific consumers.

Palmester 1543 Ethylhexyl Palmitate holds KOSHER certification, appealing to those who adhere to kosher dietary practices.
As an emollient, it helps improve the texture of cosmetic products, leaving the skin soft and smooth.
Palmester 1543 Ethylhexyl Palmitate's use of renewable vegetable oils aligns with the growing demand for sustainable ingredients.

Palmester 1543 Ethylhexyl Palmitate is known for its lightweight and non-greasy texture, making it suitable for various formulations.
Palmester 1543 Ethylhexyl Palmitate is a compound carefully crafted for fragrance use, enhancing the olfactory experience of cosmetic products.
Palmester 1543 Ethylhexyl Palmitate's compatibility with the skin makes it a favored ingredient in night creams for its moisturizing effects.

Palmester 1543 Ethylhexyl Palmitate is a crucial component in formulations where keeping qualities and stability are paramount.
Palmester 1543 Ethylhexyl Palmitate's biodegradability underscores its commitment to environmentally conscious cosmetic production.
Cosmetic products containing Palmester 1543 Ethylhexyl Palmitate are formulated to meet high standards for quality and safety.

The absence of genetically modified organisms ensures a cleaner and more natural cosmetic ingredient.
Palmester 1543 Ethylhexyl Palmitate is a versatile and reliable choice for formulators seeking an effective and sustainable emollient.



PROPERTIES


Chemical Structure: Ethylhexyl Palmitate is a fatty acid ester with the chemical formula C26H52O2.
Type: Synthetic ester.
Source: Derived from renewable vegetable oils.
Appearance: Typically a colorless liquid.
Odor: Odorless or has a mild, characteristic odor.
Texture: Emollient with a smooth and silky texture.
Function: Acts as an emollient, providing a soft and smooth feel to the skin.
Fragrance Enhancer: Used to enhance the fragrance in cosmetic formulations.
Biodegradability: Readily biodegradable, indicating environmentally friendly characteristics.
Boiling Point: 398.93°C
Melting Point: 2°C
Solubility: Soluble in chloroform and hexanes



FIRST AID


Inhalation:

Move the person to fresh air.
If breathing is difficult, administer oxygen.
Seek medical attention if symptoms persist.


Skin Contact:

Remove contaminated clothing.
Wash the affected area with plenty of water and mild soap.
If irritation persists, seek medical attention.


Eye Contact:

Rinse eyes thoroughly with water for at least 15 minutes, holding eyelids open.
Seek immediate medical attention if irritation or redness persists.


Ingestion:

Do not induce vomiting unless directed by medical personnel.
Rinse mouth with water if the person is conscious.
Seek medical attention.


General Advice:

In all cases, if symptoms persist or if there is uncertainty about the severity of exposure, seek medical attention promptly.
Provide the medical personnel with information about the specific chemical involved.



HANDLING AND STORAGE


General Handling Guidelines:

Personal Protection:
Use appropriate personal protective equipment (PPE) such as gloves, safety glasses, and protective clothing.
Follow workplace safety guidelines and practices.

Ventilation:
Use the product in well-ventilated areas or under local exhaust ventilation.

Avoidance of Contact:
Avoid direct skin contact and inhalation of vapors or mists.
Wash hands thoroughly after handling.

Preventive Measures:
Implement good industrial hygiene practices.
Do not eat, drink, or smoke while handling the substance.

Spill and Leak Response:
Implement spill control measures to contain and clean up spills promptly.
Use appropriate absorbent materials.
Dispose of waste in accordance with local regulations.


General Storage Guidelines:

Storage Conditions:
Store Ethylhexyl Palmitate in a cool, dry, and well-ventilated area.
Keep away from incompatible materials (as specified in the SDS).
Store away from direct sunlight.

Temperature Control:
Store at temperatures specified by the manufacturer.
Avoid extreme temperatures.

Container Integrity:
Ensure containers are tightly closed and properly labeled.
Check containers regularly for leaks or damage.

Segregation:
Store away from incompatible materials, as indicated in the SDS.

Specific Storage Requirements:
Follow any specific storage requirements outlined in the SDS.

Handling Cautions:
Follow proper lifting and handling procedures to prevent injuries.

Fire Prevention:
Keep away from ignition sources.
Store away from flammable materials.
PALMESTER 1545 ETHYLHEXYL STEARATE

Palmester 1545 Ethylhexyl Stearate is a versatile cosmetic ingredient known for its emollient properties.
Derived from renewable vegetable oils, it aligns with a sustainable and eco-friendly approach.
Palmester 1545 Ethylhexyl Stearate has a smooth, silky texture that contributes to the luxurious feel of cosmetic products.

CAS Number: 22047-49-0
EC Number: 244-754-0

Ethylhexyl Stearate, Palmester 1545, Stearyl Ethylhexyl Ester, Ethylhexyl Stearate Palmester 1545, Stearyl Ester of Ethylhexyl Stearate, Ester of Ethylhexyl Stearate, Stearyl Ethylhexyl Stearate, Ethylhexyl Ester of Stearyl Stearate, Palmester 1545 Stearyl Ester, Stearyl Ester of Palmester 1545, Ethylhexyl Stearate 1545, Palmester 1545 Ethylhexyl Ester, Stearyl Ester 1545, Ester of Palmester 1545, Stearyl Ester of Ethylhexyl Stearate 1545, Ethylhexyl Stearate Ester, Stearyl Ethylhexyl Ester 1545, Palmester 1545 Stearyl Ethylhexyl Ester, Stearyl Stearate Ethylhexyl Ester, Ethylhexyl Stearate Palmester 1545 Ester, Stearyl Ester of Ethylhexyl Stearate Palmester 1545, Ester of Stearyl Ethylhexyl Stearate, Ethylhexyl Ester Stearyl Stearate, Palmester 1545 Stearyl Ethylhexyl Stearate, Ethylhexyl Stearate 1545 Ester, Palmester 1545 Ethylhexyl Stearate Ester, Stearyl Ester 1545 Ethylhexyl Stearate, Ester of Palmester 1545 Stearyl, Ethylhexyl Stearate Ester 1545, Stearyl Ester of Palmester 1545 Ethylhexyl Stearate, Palmester 1545 Stearyl Ester of Ethylhexyl Stearate, Stearyl Stearate Ethylhexyl Ester Palmester 1545, Ethylhexyl Stearate Palmester 1545 Stearyl Ester, Stearyl Ester 1545 Ethylhexyl Stearate Palmester 1545, Ester of Stearyl Ethylhexyl Stearate Palmester 1545, Ethylhexyl Ester Stearyl Stearate 1545, Palmester 1545 Stearyl Ethylhexyl Stearate Ester, Stearyl Ester of Ethylhexyl Stearate Palmester 1545, Ester of Palmester 1545 Ethylhexyl Stearate, Stearyl Ethylhexyl Ester 1545 Palmester 1545, Ethylhexyl Stearate Ester Palmester 1545, Stearyl Stearate Ethylhexyl Ester 1545, Palmester 1545 Stearyl Ester of Ethylhexyl Stearate, Ester of Stearyl Ethylhexyl Stearate 1545, Ethylhexyl Ester Stearyl Stearate Palmester 1545, Stearyl Ester 1545 Ethylhexyl Stearate Ester, Ester of Palmester 1545 Stearyl Ethylhexyl Stearate, Stearyl Ethylhexyl Stearate Palmester 1545 Ester, Ethylhexyl Stearate 1545 Ester Stearyl, Palmester 1545 Stearyl Ester 1545 Ethylhexyl Stearate, Stearyl Ester of Ethylhexyl Stearate Palmester 1545 Ethylhexyl Stearate, Ester of Palmester 1545 Stearyl Ethylhexyl Stearate Ester, Ethylhexyl Ester Stearyl Stearate 1545 Palmester 1545, Stearyl Ester 1545 Ethylhexyl Stearate Palmester 1545 Ester



APPLICATIONS


Palmester 1545 Ethylhexyl Stearate is commonly utilized as an emollient in a wide range of cosmetic products.
Night creams often incorporate Palmester 1545 Ethylhexyl Stearate to provide effective moisturization and enhance skin texture.

Hand creams benefit from the skin-conditioning properties of Palmester 1545 Ethylhexyl Stearate, promoting soft and nourished hands.
Cleansing lotions enriched with this compound offer a gentle and smooth cleansing experience.
Baby creams utilize Palmester 1545 Ethylhexyl Stearate for its emollient nature, suitable for delicate and sensitive baby skin.

Massage lotions containing this ester enhance the glide during massages, providing a luxurious feel.
Its use extends to various cosmetic care products, contributing to the overall formulation's efficacy.
Facial serums and treatments leverage the spreadability and absorption-enhancing properties of Palmester 1545 Ethylhexyl Stearate.

Makeup formulations, including foundations, may feature this compound for a smoother and more even application.
The ester serves as a fragrance enhancer, contributing to a pleasant olfactory experience in cosmetic products.
Palmester 1545 Ethylhexyl Stearate is a suitable replacement for mineral oil in cosmetic formulations.

Sunscreen formulations benefit from this ester's properties, improving spreadability and skin-feel.
Lip balms may include Palmester 1545 Ethylhexyl Stearate to provide a soft and moisturizing texture to the lips.

Body lotions and creams often feature this compound to impart a silky and non-greasy finish on the skin.
Anti-aging creams may incorporate Palmester 1545 Ethylhexyl Stearate for its skin-conditioning and moisturizing benefits.

The ester is used in formulations targeting specific skin concerns, such as dry or chapped skin.
Hair care products, including leave-in conditioners, may contain this compound for its conditioning properties.
Palmester 1545 Ethylhexyl Stearate is found in cosmetic wipes and towelettes for its skin-conditioning effects.
Deodorant formulations may utilize this ester to enhance the glide and spreadability of the product.

Inclusion in facial masks contributes to the product's texture and overall skin-conditioning properties.
Cosmetic products designed for men, such as beard oils and grooming products, may contain this compound.

Palmester 1545 Ethylhexyl Stearate is employed in formulations targeting specific skin types, including sensitive or reactive skin.
Moisturizing body washes and shower gels may include this ester for its skin-friendly and emollient nature.
Palmester 1545 Ethylhexyl Stearate can be part of the ingredients in bath oils and bath bombs, providing a luxurious bathing experience.
Palmester 1545 Ethylhexyl Stearate is a versatile ingredient, making it suitable for a diverse range of cosmetic and personal care applications.

Palmester 1545 Ethylhexyl Stearate is a common inclusion in cosmetic serums, contributing to their smooth texture and ease of application.
Its emollient properties make it a valuable ingredient in body butter formulations, ensuring deep moisturization.

Palmester 1545 Ethylhexyl Stearate is utilized in skin balms to provide a protective barrier and prevent moisture loss.
Palmester 1545 Ethylhexyl Stearate can be found in sunless tanning lotions and sprays, enhancing the application and skin-feel.

Palmester 1545 Ethylhexyl Stearate is used in powder formulations, such as blushes and bronzers, for its blending capabilities.
In makeup primers, Palmester 1545 Ethylhexyl Stearate contributes to a smooth canvas for subsequent makeup application.

Its skin-conditioning effects make it a beneficial ingredient in cuticle oils for nail care.
Eyebrow pomades may include this compound for its contribution to a creamy and easily applicable texture.
Palmester 1545 Ethylhexyl Stearate enhances the overall feel of exfoliating scrubs and contributes to a silky finish.

Personal lubricants and intimate care products utilize this ester for its skin-friendly properties.
Palmester 1545 Ethylhexyl Stearate may be present in dry shampoo formulations to impart conditioning benefits to the hair.

Included in shaving creams, it provides lubrication and a smooth glide during shaving.
Palmester 1545 Ethylhexyl Stearate contributes to the silky texture of body powders, ensuring a comfortable application.
Deodorants and antiperspirants may contain this ester for its skin-friendly and emollient effects.
In matte lipsticks, it aids in achieving a non-drying formula while providing a desirable texture.

Palmester 1545 Ethylhexyl Stearate is utilized in cosmetic pencils, ensuring a creamy and easily blendable consistency.
Included in foot creams, it helps soften and moisturize dry and rough skin on the feet.
Some nail polishes may contain Palmester 1545 for its contribution to a smooth and glossy finish.

Its texture-enhancing properties make it suitable for inclusion in eye shadow formulations.
Palmester 1545 Ethylhexyl Stearate is used in eyeliner gels for its ability to contribute to a long-lasting and smudge-resistant formula.
Cosmetic products for makeup removal benefit from the ester's gentle and skin-conditioning nature.

Included in facial mists, it contributes to a lightweight and refreshing application on the skin.
Palmester 1545 Ethylhexyl Stearate may be found in liquid foundation formulations to improve spreadability and blendability.
Men's grooming products like beard creams and grooming lotions may feature this compound for its skin-friendly properties.
The ester enhances the even distribution of fragrance in body mists, providing a longer-lasting scent.

Its conditioning properties make Palmester 1545 a valuable ingredient in leave-in hair conditioners.
Palmester 1545 Ethylhexyl Stearate contributes to the luxurious texture of hair masks, providing deep nourishment to the hair.

Included in liquid highlighters, this ester aids in achieving a smooth and blendable consistency on the skin.
Palmester 1545 Ethylhexyl Stearate enhances the moisturizing effect of shower oils, leaving the skin soft and hydrated.
Palmester 1545 Ethylhexyl Stearate is used in body scrubs to improve the overall sensory experience during exfoliation.
In tattoo creams and aftercare lotions, it helps soothe and moisturize the skin.

Palmester 1545 Ethylhexyl Stearate contributes to the glossy and non-sticky texture of lip gloss formulations.
Included in insect repellent creams, it aids in creating a smooth and easy-to-apply formula.
Its emollient nature is beneficial in hand sanitizers, preventing skin dryness often associated with frequent use.

In tinted moisturizers, it improves the spreadability of pigments for a more even skin tone.
Palmester 1545 Ethylhexyl Stearate is used in body shimmers to provide a radiant and shimmering effect on the skin.

Palmester 1545 Ethylhexyl Stearate contributes to the creamy texture of eyeshadows, ensuring easy application and blending.
Included in foot sprays, it improves the application and overall comfort of the product.

In hydrating face mists, it enhances the skin's moisture levels with a lightweight application.
Palmester 1545 Ethylhexyl Stearate is featured in overnight masks, providing prolonged skin-conditioning benefits.
In body balms, it offers a rich and indulgent texture, ideal for intensive skin moisturization.

Its emollient properties make it suitable for cuticle creams, promoting healthy nails.
Used in liquid blush formulations, it aids in achieving a natural and dewy finish on the cheeks.
Palmester 1545 Ethylhexyl Stearate may be present in oil-based perfumes, contributing to a long-lasting fragrance on the skin.
In hydroalcoholic gels, it can help counteract the drying effects of alcohol on the skin.
Included in cleansing oils, it assists in the gentle removal of makeup and impurities.

Its use in body creams for expectant mothers addresses skin changes during and after pregnancy.
Palmester 1545 Ethylhexyl Stearate is utilized in solid perfumes for its solidifying and skin-conditioning qualities.
In bronzing lotions, it enhances the application and ensures an even distribution of color.
Included in skin-perfecting primers, it creates a smooth base for flawless makeup application.



DESCRIPTION


Palmester 1545 Ethylhexyl Stearate is a versatile cosmetic ingredient known for its emollient properties.
Derived from renewable vegetable oils, it aligns with a sustainable and eco-friendly approach.
Palmester 1545 Ethylhexyl Stearate has a smooth, silky texture that contributes to the luxurious feel of cosmetic products.

With its excellent emollient nature, it imparts a soft and velvety touch to the skin upon application.
As a GMO-free compound, Palmester 1545 Ethylhexyl Stearate assures consumers of its commitment to avoiding genetically modified organisms.

The safety profile is enhanced by being Bovine Spongiform Encephalopathy/Transmissible Spongiform Encephalopathy-free.
Palmester 1545 Ethylhexyl Stearate can effectively replace mineral oil in various cosmetic formulations.
Night creams benefit from its inclusion, providing moisturization and promoting skin comfort.

Its application extends to hand creams, offering skin-conditioning benefits for the hands.
Cleansing lotions containing this ester ensure a gentle and nourishing cleansing experience.
Baby creams incorporate Palmester 1545 Ethylhexyl Stearate for its emollient and skin-friendly characteristics.
Massage lotions are enriched with the ester, enhancing the overall sensory experience during massages.

Its HALAL and KOSHER certifications make it suitable for consumers adhering to specific dietary requirements.
Palmester 1545 Ethylhexyl Stearate stands out for its broad use in cosmetic care products, showcasing its versatility.

Facial serums and treatments benefit from its spreadability and absorption-enhancing properties.
Palmester 1545 Ethylhexyl Stearate, as a fragrance enhancer, contributes to a pleasing olfactory experience in cosmetic formulations.
Palmester 1545 Ethylhexyl Stearate's non-greasy feel makes it an ideal choice for formulations where light texture is desired.
Body lotions containing this compound provide a silky and non-greasy finish on the skin.
Its compatibility with different skin types, including sensitive skin, adds to its appeal.

Palmester 1545 Ethylhexyl Stearate contributes to the stability and shelf life of cosmetic products, ensuring product quality.
Palmester 1545 Ethylhexyl Stearate's biodegradability aligns with the growing demand for environmentally conscious cosmetic ingredients.
Inclusion in makeup products, such as foundations, enhances the smooth application and blendability.

Sunscreen formulations may feature this ester for improved spreadability and skin-feel.
Its use in anti-aging creams showcases its moisturizing and skin-conditioning benefits for mature skin.
Palmester 1545 Ethylhexyl Stearate stands as a testament to the combination of efficacy, safety, and sustainability in cosmetic formulations.



PROPERTIES


Boiling Point: 426.2°C
Melting Point: -45°C
pH: Neutral
Solubility: Insoluble in water
Viscosity: Low



FIRST AID


Inhalation:

If inhaled, move the affected person to fresh air.
If breathing difficulties persist, seek medical attention.


Skin Contact:

In case of skin contact, remove contaminated clothing.
Wash the affected area with plenty of soap and water.
If irritation or redness occurs, seek medical advice.


Eye Contact:

In case of contact with eyes, rinse cautiously with water for several minutes, removing contact lenses if present.
Seek medical attention if irritation persists.


Ingestion:

If swallowed, do not induce vomiting unless directed by medical personnel.
Rinse mouth with water and seek immediate medical attention.


Notes to Physicians:

Treat symptomatically based on individual reactions.
Provide supportive care as necessary.


Firefighting Measures:

Extinguishing Media:

Use fire-extinguishing media suitable for surrounding materials (e.g., water spray, foam, dry chemical).


Special Firefighting Procedures:

Wear appropriate protective equipment.
Evacuate the area if the fire is uncontrollable.


Unusual Fire and Explosion Hazards:

No unusual fire or explosion hazards reported.



HANDLING AND STORAGE


Handling:

Handling Procedures:
Follow good industrial hygiene practices during handling.
Wash hands thoroughly after handling and before eating, drinking, or smoking.

Protection Against Fire and Explosion:
Take measures to prevent the buildup of electrostatic charges.
Use explosion-proof equipment if applicable.

Ventilation:
Ensure adequate ventilation in areas where the product is handled or processed.
Use local exhaust ventilation if necessary to control airborne concentrations.

Protective Measures:
Wear appropriate personal protective equipment (PPE), including gloves, safety goggles, and protective clothing.
Use respiratory protection if exposure limits are exceeded.

Storage Compatibility:
Store away from incompatible materials and substances.
Check the SDS for specific information on substances to avoid.

Handling Precautions:
Avoid contact with eyes, skin, and clothing.
Do not eat, drink, or smoke while handling the product.
Avoid inhalation of vapors or dust.


Storage:

Storage Conditions:
Store in a cool, dry, and well-ventilated area.
Keep away from heat sources, direct sunlight, and open flames.

Storage Temperature:
Store within a specified temperature range, as indicated in the SDS.

Storage Containers:
Use approved containers made of compatible materials.
Keep containers tightly closed when not in use to prevent contamination.

Incompatible Materials:
Store away from incompatible materials, as listed in the SDS.

Specific End Uses:
Store the product in a manner consistent with its intended applications.

Control Measures:
Implement engineering controls to minimize exposure during storage.
Use secondary containment to prevent spills from reaching the environment.

Handling of Leaked or Spilled Material:
Clean up spills immediately, following appropriate safety measures.
Dispose of waste in accordance with local regulations.

Storage Stability:
Check the product's stability over time and adhere to expiration dates if applicable.

Special Precautions:
Follow any specific precautions or recommendations provided in the SDS.

Security Measures:
Implement security measures to prevent unauthorized access or theft.
PALMESTER 3595 CAPRYLIC/CAPRIC TRIGLYCERIDE (MCT)

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is a chemical compound commonly known as Medium-Chain Triglycerides (MCT).
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is a type of fatty acid ester derived from coconut oil or palm kernel oil.
MCTs are composed of medium-chain fatty acids, specifically caprylic acid (8 carbons) and capric acid (10 carbons).
The triglyceride structure refers to the glycerol molecule combined with three fatty acid chains.

CAS Number: 65381-09-1
EC Number: 265-724-3

Caprylic/Capric Triglyceride, MCT, Medium-Chain Triglycerides, Palmester 3595, Fractionated Coconut Oil, Coconut Triglycerides, Capryl Capric Triglycerides, Caprylic Capric Acid Triglyceride, Mixed Triglycerides, C8/C10 Triglycerides, Caprylic Capric Glycerides, Caprylic Glycerides, Capric Glycerides, Caprylic Fatty Acid Triglyceride, Capric Fatty Acid Triglyceride, Medium-Chain Fatty Acid Ester, Caprylic/Capric Acid Ester, MCT Oil, Caprylic Capric Ester, Medium-Chain Ester, Caprylic Capric Ester of Glycerin, Triglycerol Ester, Capryl Caprylate, Capric Caprylate, Glycerin Ester of Medium-Chain Fatty Acids, Glycerol Triester of Caprylic/Capric Acids, MCT Triglyceride, Coconut Oil Ester, Medium-Chain Glyceride, Caprylic Capric Glycerol Ester, Glyceride of Coconut Oil, Coconut Fatty Acid Triglyceride, Capric Fatty Acids Glyceride, Medium-Chain Fatty Acid Triglyceride, Triglyceride of Caprylic/Capric Acids, MCT Glyceride, Medium-Chain Coconut Oil Ester, Coconut Oil Triglycerol Ester, Capric Glycerol Triglyceride, Caprylic Glycerol Triglyceride, Caprylic Capric Triester of Glycerol, Glycerol Triglyceride of Medium-Chain Fatty Acids, MCT Esters, Caprylic Capric Oil, Glyceride of Fractionated Coconut Oil, Caprylic Ester of Glycerol, Capric Ester of Glycerol, Medium-Chain Triglycerol Ester, Glycerol Triester of Caprylic/Capric Fatty Acids, Coconut Oil Fatty Acids Glyceride, MCT Fraction, Caprylic Glycerol Ester of Fatty Acids, Capric Glycerol Ester of Fatty Acids, Medium-Chain Fatty Acid Glyceride, Caprylic/Capric Acid Ester of Glycerol.



APPLICATIONS


Palmester 3595 Caprylic/Capric Triglyceride (MCT) is a commonly used ingredient in skincare products such as moisturizers and lotions.
Its emollient properties make it a valuable component in formulations designed to soften and hydrate the skin.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is often found in facial cleansers, contributing to a gentle and effective cleansing experience.

In the cosmetics industry, it is a popular choice for foundations and concealers, providing a smooth and even application.
Sunscreen formulations often include Palmester 3595 Caprylic/Capric Triglyceride (MCT) to enhance spreadability and skin-feel.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) serves as a carrier oil for essential oils in aromatherapy and fragrance applications.
Massage oils frequently contain this compound for its lightweight texture and ease of glide.
Due to its stability and compatibility, it is used in a variety of haircare products, including conditioners and styling products.
Lip balms utilize Palmester 3595 Caprylic/Capric Triglyceride (MCT) to impart a soft and moisturizing feel to the lips.

In anti-aging creams, Palmester 3595 Caprylic/Capric Triglyceride (MCT) contributes to the overall texture and helps deliver active ingredients to the skin.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is present in bath oils and bath bombs, enhancing the bathing experience with its emollient properties.

Makeup removers often contain Palmester 3595 Caprylic/Capric Triglyceride (MCT) for its ability to dissolve makeup while leaving the skin feeling nourished.
Baby care products, including diaper creams and lotions, may feature Palmester 3595 Caprylic/Capric Triglyceride (MCT) for its gentle and skin-friendly nature.

Hand creams use Palmester 3595 Caprylic/Capric Triglyceride (MCT) to provide effective moisturization and combat dryness.
In deodorants and antiperspirants, Palmester 3595 Caprylic/Capric Triglyceride (MCT) assists in creating a smooth and comfortable application.
Fragrance formulations benefit from its solvent properties, helping to disperse and enhance the longevity of scents.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is utilized in the production of bath and shower gels for its emollient and cleansing characteristics.
Body scrubs often incorporate this compound to enhance the exfoliation process and leave the skin feeling soft.
In hair serums and leave-in treatments, Palmester 3595 Caprylic/Capric Triglyceride (MCT) helps in detangling and adding a silky shine to the hair.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is a common ingredient in personal lubricants for its skin-friendly and lubricating properties.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is featured in facial masks to improve the spreadability and overall texture of the product.
Foot creams use Caprylic/Capric Triglyceride to moisturize and soften the skin on the feet.
Tattoo aftercare products may contain Palmester 3595 Caprylic/Capric Triglyceride (MCT) for its soothing and skin-conditioning effects.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is used in cosmetic wipes and towelettes for its emollient properties.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is found in shaving creams to provide lubrication and a smooth shaving experience.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is a key ingredient in body lotions and creams, contributing to their luxurious texture and moisturizing properties.
Nail care products, such as cuticle creams and oils, often include MCT to nourish and condition the nails and surrounding skin.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is used in sunless tanning products to provide an even application and enhance the absorption of tanning agents.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is a common component in natural and organic skincare formulations due to its renewable sourcing and eco-friendly profile.
Eyebrow pencils and pomades may contain Palmester 3595 Caprylic/Capric Triglyceride (MCT) for its role in creating a smooth and blendable consistency.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is present in dry shampoos, contributing to their lightweight and non-greasy formulation.
Shampoo formulations may include Palmester 3595 Caprylic/Capric Triglyceride (MCT) to enhance the overall feel and manageability of the hair.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is utilized in bath salts and bath oils to disperse essential oils and provide skin-conditioning benefits.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is found in intimate care products, such as personal lubricants, for its gentle and non-irritating properties.
Some natural and organic deodorants use Palmester 3595 Caprylic/Capric Triglyceride (MCT) for its skin-friendly nature and compatibility with other natural ingredients.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is employed in lip care products, including lip glosses and balms, for its moisturizing and glossy effects.
Tattoo inks may contain Palmester 3595 Caprylic/Capric Triglyceride (MCT) to improve pigment dispersion and application.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is used in shaving foams and gels to provide a smooth glide and reduce friction during shaving.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is featured in facial serums to enhance the delivery of active ingredients and promote skin health.
Natural and organic mascaras may incorporate Palmester 3595 Caprylic/Capric Triglyceride (MCT) for its lightweight and conditioning properties.
In body mists and sprays, the compound aids in even fragrance distribution and provides a non-greasy finish.
Hair masks and deep conditioning treatments often include Palmester 3595 Caprylic/Capric Triglyceride (MCT) for its ability to nourish and revitalize hair strands.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is used in acne treatment products to deliver active ingredients without causing excessive dryness.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is found in solid perfumes, contributing to their smooth and easily applicable consistency.
Makeup setting sprays may contain Palmester 3595 Caprylic/Capric Triglyceride (MCT) for its ability to set makeup without compromising its appearance.
Some natural and organic insect repellents use Caprylic/Capric Triglyceride as a base for essential oil blends.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is used in natural and mineral-based foundations to improve the spreadability and blendability of pigments.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is present in baby wipes for its gentle and moisturizing qualities.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is utilized in hand sanitizers to counteract the drying effects of alcohol and provide a skin-conditioning element.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is a versatile ingredient in the formulation of various cosmetic and personal care products, showcasing its adaptability to different applications.

Hair styling products, including hair sprays and gels, may incorporate Caprylic/Capric Triglyceride for its lightweight and non-sticky feel.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is a common ingredient in cuticle oils, providing nourishment and promoting healthy nails.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is used in foot creams to soften and moisturize dry and rough skin on the feet.

Some natural and organic foundations use Palmester 3595 Caprylic/Capric Triglyceride (MCT) as a base to create a smooth and buildable coverage.
Nail polish removers may contain this compound to help dissolve nail polish while conditioning the nails.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is employed in beard oils to soften facial hair and moisturize the underlying skin.
Scalp treatments, including serums and oils, may include Caprylic/Capric Triglyceride for its conditioning effects on the scalp.
Natural and organic baby lotions use this compound for its gentle and non-irritating properties on delicate baby skin.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is found in anti-chafing products to provide a smooth and friction-reducing barrier on the skin.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is utilized in after-sun care products to soothe and moisturize sun-exposed skin.
Some natural and organic blushes incorporate MCT for its ability to blend seamlessly and provide a natural-looking flush.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is a common ingredient in cuticle balms, aiding in the maintenance of healthy and hydrated cuticles.
Beard balms may include Palmester 3595 Caprylic/Capric Triglyceride (MCT) to soften facial hair and impart a subtle sheen.
Natural and organic mascara formulations may use MCT for its conditioning and non-clumping properties.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is featured in hand masks to provide intensive moisturization and rejuvenation.

Lip scrubs often contain this compound to aid in exfoliating and smoothing the lips.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is used in natural and organic sunscreens for its ability to enhance the even distribution of UV filters.
In natural and organic eyeliners, Palmester 3595 Caprylic/Capric Triglyceride (MCT) contributes to a smooth and easily applicable texture.

Some natural and organic dry body oils use Caprylic/Capric Triglyceride for a lightweight and non-greasy finish.
Foot scrubs may incorporate this compound for its emollient properties, leaving the feet soft and refreshed.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is used in cuticle serums to nourish and condition the nail beds.
Natural and organic night creams may contain MCT for its skin-conditioning and rejuvenating effects.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is found in natural and organic makeup removers to dissolve makeup while leaving the skin nourished.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is used in natural and organic lip balms to provide hydration and prevent dryness.
In natural and organic setting powders, MCT may contribute to a lightweight and finely milled texture for a seamless finish.



DESCRIPTION


Palmester 3595 Caprylic/Capric Triglyceride (MCT) is a chemical compound commonly known as Medium-Chain Triglycerides (MCT).
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is a type of fatty acid ester derived from coconut oil or palm kernel oil.
MCTs are composed of medium-chain fatty acids, specifically caprylic acid (8 carbons) and capric acid (10 carbons).
The triglyceride structure refers to the glycerol molecule combined with three fatty acid chains.

Palmester 3595 Caprylic/Capric Triglyceride (MCT), commonly known as MCT, is a versatile and widely used chemical compound.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) stands out as a colorless and odorless liquid with a smooth, silky texture.

Derived from renewable sources such as coconut or palm kernel oil, it aligns with sustainable and eco-friendly practices.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is composed of medium-chain fatty acids, specifically caprylic acid and capric acid.

With its excellent emollient properties, Palmester 3595 Caprylic/Capric Triglyceride (MCT) is a popular choice in skincare products for its ability to soften and smooth the skin.
Its lightweight and non-greasy feel make it an ideal ingredient in cosmetic formulations, ranging from lotions to serums.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) serves as a solvent for fragrances, enhancing their dispersion and overall effectiveness in various products.

The triglyceride structure of Palmester 3595 Caprylic/Capric Triglyceride (MCT), combined with glycerol, contributes to its stability under different conditions.
Recognized for its compatibility with different skin types, it is often included in formulations for sensitive skin.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is a common ingredient in massage oils, contributing to a luxurious and gliding sensation during massages.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) has a neutral scent, making it an excellent carrier for both fragranced and fragrance-free cosmetic products.
Due to its stability, MCT helps extend the shelf life of formulations, ensuring product quality over time.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) plays a crucial role in skincare products designed for hydration and moisturization, promoting skin health.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is an ester of glycerol and medium-chain fatty acids, offering enhanced solubility in both water and oil.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is recognized for its ability to enhance the spreadability and absorption of active ingredients in formulations.

As a GMO-free ingredient, MCT assures consumers of its commitment to avoiding genetically modified organisms.
Its presence in cosmetic formulations contributes to a pleasant sensory experience, leaving a silky and non-greasy finish on the skin.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is often used in formulations targeting specific skin concerns, such as dryness or roughness.
The clear and transparent nature of MCT allows it to be seamlessly incorporated into various cosmetic products without altering their appearance.

Palmester 3595 Caprylic/Capric Triglyceride (MCT)'s emollient nature makes it suitable for use in haircare products, providing conditioning benefits to the hair.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is known for its versatility in formulations, ranging from skincare creams to makeup products like foundations and lip balms.
Its inclusion in sunscreens contributes to improved spreadability and a comfortable skin-feel during application.
Palmester 3595 Caprylic/Capric Triglyceride (MCT) is HALAL and KOSHER certified, meeting specific dietary requirements and preferences.

Palmester 3595 Caprylic/Capric Triglyceride (MCT) is a key ingredient in environmentally conscious formulations due to its renewable sourcing and biodegradability.
Its widespread use across the cosmetic and personal care industry attests to MCT's efficacy, safety, and multifunctional qualities.



PROPERTIES


Boiling Point: 270°C
Solubility: Soluble in water
Viscosity: 25-33 cP



FIRST AID


Inhalation:

If inhaled, move the affected person to fresh air.
If breathing difficulties persist, seek medical attention.


Skin Contact:

In case of skin contact, remove contaminated clothing.
Wash the affected area with plenty of soap and water.
If irritation or redness occurs, seek medical advice.


Eye Contact:

In case of contact with eyes, rinse cautiously with water for several minutes, removing contact lenses if present.
Seek medical attention if irritation persists.


Ingestion:

If swallowed, do not induce vomiting unless directed by medical personnel.
Rinse mouth with water and seek immediate medical attention.



HANDLING AND STORAGE


Handling:

Handling Procedures:
Follow good industrial hygiene practices during handling.
Wash hands thoroughly after handling and before eating, drinking, or smoking.

Protection Against Fire and Explosion:
Take measures to prevent the buildup of electrostatic charges.
Use explosion-proof equipment if applicable.

Ventilation:
Ensure adequate ventilation in areas where the product is handled or processed.
Use local exhaust ventilation if necessary to control airborne concentrations.

Protective Measures:
Wear appropriate personal protective equipment (PPE), including gloves, safety goggles, and protective clothing.
Use respiratory protection if exposure limits are exceeded.

Storage Compatibility:
Store away from incompatible materials and substances.
Check the SDS for specific information on substances to avoid.

Handling Precautions:
Avoid contact with eyes, skin, and clothing.
Do not eat, drink, or smoke while handling the product.
Avoid inhalation of vapors or dust.


Storage:

Storage Conditions:
Store in a cool, dry, and well-ventilated area.
Keep away from heat sources, direct sunlight, and open flames.

Storage Temperature:
Store within a specified temperature range, as indicated in the SDS.

Storage Containers:
Use approved containers made of compatible materials.
Keep containers tightly closed when not in use to prevent contamination.

Incompatible Materials:
Store away from incompatible materials, as listed in the SDS.

Specific End Uses:
Store the product in a manner consistent with its intended applications.

Control Measures:
Implement engineering controls to minimize exposure during storage.
Use secondary containment to prevent spills from reaching the environment.

Handling of Leaked or Spilled Material:
Clean up spills immediately, following appropriate safety measures.
Dispose of waste in accordance with local regulations.

Storage Stability:
Check the product's stability over time and adhere to expiration dates if applicable.
PALMITIC ACID
SYNONYMS n-Hexadecoic acid; Pentadecanecarboxylic acid; n-Hexadecanoic acid; 1-Pentadecanecarboxylic acid; Cetylic acid; Hexadecylic acid; (EDENOR C1698) CAS NO. 57-10-3
PALMITIC ACID
Palmitic Acid is a kind of common saturated fatty acid of a 16-carbon backbone, which is contained in fats and waxes.
Palmitic Acid naturally exists in palm oil and palm kernel oil, and can also be found in butter, cheese, milk, meat, cocoa butter, soybean oil and sunflower oil.
Palmitic Acid can be produced by many kinds of plants and organisms.

CAS: 57-10-3
MF: C16H32O2
MW: 256.42
EINECS: 200-312-9

Synonms
Palmitic acid, Hexadecanoic acid, 57-10-3, Cetylic acid, palmitate, n-Hexadecanoic acid, Hexadecylic acid, Hydrofol, n-Hexadecoic acid, 1-Pentadecanecarboxylic acid, Palmitinic acid, hexaectylic acid, Pentadecanecarboxylic acid, hexadecoic acid, 1-Hexyldecanoic Acid, Industrene 4516, Emersol 140, Emersol 143, Hystrene 8016, Hystrene 9016, Palmitinsaeure, Palmitic acid, pure, Palmitic acid 95%, Kortacid 1698, FEMA No. 2832, Loxiol EP 278, Palmitic acid (natural), Hydrofol Acid 1690, Cetyl acid, Prifac 2960, C16:0, HSDB 5001, Pristerene 4934, Pristerene-4934, Edenor C16, NSC 5030, AI3-01594, Lunac P 95KC, Lunac P 95, Lunac P 98, CCRIS 5443, Prifac-2960, CHEBI:15756, NSC5030, NSC-5030, EINECS 200-312-9, UNII-2V16EO95H1, FA 16:0, BRN 0607489, Palmitic acid (NF), DTXSID2021602, Glycon P-45, IMEX C 1498, 2V16EO95H1, Hexadecanoic acid (9CI), MFCD00002747, Palmitic acid (7CI,8CI), CHEMBL82293, DTXCID101602, 67701-02-4, CH3-[CH2]14-COOH, EC 200-312-9, 4-02-00-01157 (Beilstein Handbook Reference), n-hexadecoate, LMFA01010001, PA 900, EDENOR C 16-98-100, FA 1695, SURFAXIN COMPONENT PALMITIC ACID, 1-hexyldecanoate, NCGC00164358-01, LUCINACTANT COMPONENT PALMITIC ACID, pentadecanecarboxylate, Hexadecanoic acid 10 microg/mL in Acetonitrile, HEXADECANOIC-11,11,12,12-D4 ACID, PALMITIC ACID (II), PALMITIC ACID [II], PALMITIC ACID (MART.), PALMITIC ACID [MART.], CH3-(CH2)14-COOH, Palmitic acid; Hexadecanoic acid, PLM, palmic acid, Hexadecanoate (n-C16:0), PALMITIC ACID (EP MONOGRAPH), PALMITIC ACID [EP MONOGRAPH], Acid, Palmitic, CAS-57-10-3, Acid, Hexadecanoic, SR-01000944716, Palmitic acid [USAN:NF], palmitoate, Hexadecoate, Palmitinate, Palmitinsaure, palmitic-acid, palmitoic acid, Hexadecanoicacid, Aethalic acid, Hexadecanoic acid Palmitic acid, 2hmb, 2hnx, Palmitic acid_jeyam, n-Hexadecyclic Acid, fatty acid 16:0, Palmitic Acid, FCC, Kortacid 1695, Palmitic acid_RaGuSa, Univol U332, 1219802-61-5, Prifrac 2960, Hexadecanoic acid anion, Hexadecanoic--d5 Acid, 3v2q, Palmitic acid, >=99%, bmse000590, Epitope ID:141181, CETYL ACID [VANDF], PALMITIC ACID [MI], SCHEMBL6177, PALMITIC ACID [DSC], PALMITIC ACID [FCC], PALMITIC ACID [FHFI], PALMITIC ACID [HSDB], PALMITIC ACID [INCI], PALMITIC ACID [USAN], FAT, WLN: QV15, P5585_SIGMA, PALMITIC ACID [VANDF], GTPL1055, QSPL 166, PALMITIC ACID [USP-RS], PALMITIC ACID [WHO-DD], (1(1)(3)C)hexadecanoic acid, 1b56, HMS3649N08, Palmitic acid, analytical standard, Palmitic acid, BioXtra, >=99%, Palmitic acid, Grade II, ~95%, HY-N0830, Palmitic acid, natural, 98%, FG, Tox21_112105, Tox21_201671, Tox21_302966, AC9381, BDBM50152850, s3794, Palmitic acid, >=95%, FCC, FG, AKOS005720983, Tox21_112105_1, CCG-267027, CR-0047, DB03796, Palmitic acid, for synthesis, 98.0%, NCGC00164358-02, NCGC00164358-03, NCGC00256424-01, NCGC00259220-01, BP-27917, Palmitic acid, purum, >=98.0% (GC), SY006518, CS-0009861, FT-0626965, FT-0772579, P0002, P1145, Palmitic acid, SAJ first grade, >=95.0%, EN300-19603, C00249, D05341, Palmitic acid, Vetec(TM) reagent grade, 98%, PALMITIC ACID (CONSTITUENT OF SPIRULINA), Palmitic acid, >=98% palmitic acid basis (GC), A831313, Q209727, PALMITIC ACID (CONSTITUENT OF FLAX SEED OIL), PALMITIC ACID (CONSTITUENT OF SAW PALMETTO), SR-01000944716-1, SR-01000944716-2, BA71C79B-C9B1-451A-A5BE-B480B5CC7D0C, PALMITIC ACID (CONSTITUENT OF BORAGE SEED OIL), PALMITIC ACID (CONSTITUENT OF SPIRULINA) [DSC], F0001-1488, Z104474418, PALMITIC ACID (CONSTITUENT OF EVENING PRIMROSE OIL), PALMITIC ACID (CONSTITUENT OF SAW PALMETTO) [DSC]

Palmitic Acid can be used for the production of soap, cosmetics, and industrial mold release agents.
Palmitic Acid is also a food processing aid. It can also be used to produce cetyl alocohol which is useful in the production of detergents and cosmetics.
Recently, Palmitic Acid has been also used for the manufacture of a long-acting antipsychotic medication, paliperidone palmitate.

Palmitic acid occurs as white crystalline scales with a slight characteristic odor and taste.
Palmitic Acid is one of the most common saturated fatty acids found in animals and plants.
Palmitic Acid is a mixture of solid organic acids obtained from fats consisting chiefly of palmitic acid (C16H35O2) with varying amounts of stearic acid (C16H36O2).
As Palmitic Acid name tells us, it is found in palm oil but also in butter, cheese, milk and meat.

Palmitic acid (hexadecanoic acid in IUPAC nomenclature) is a fatty acid with a 16-carbon chain.
Palmitic Acid is the most common saturated fatty acid found in animals, plants and microorganisms.
Palmitic Acid chemical formula is CH3(CH2)14COOH, and its C:D (the total number of carbon atoms to the number of carbon–carbon double bonds) is 16:0.
Palmitic Acid is a major component of the oil from the fruit of oil palms (palm oil), making up to 44% of total fats.
Meats, cheeses, butter, and other dairy products also contain palmitic acid, amounting to 50–60% of total fats.
Palmitates are the salts and esters of palmitic acid.
The palmitate anion is the observed form of palmitic acid at physiologic pH (7.4).
Major sources of C16:0 are palm oil, palm kernel oil, coconut oil, and milk fat

Palmitic Acid Chemical Properties
Melting point: 61-62.5 °C(lit.)
Boiling point: 351.5 °C
density: 0.852 g/mL at 25 °C(lit.)
vapor pressure: 10 mm Hg ( 210 °C)
refractive index 1.4273
FEMA: 2832 | PALMITIC ACID
Fp: >230 °F
storage temp.: room temp
solubility: chloroform: 0.5 M, clear, colorless
form: Flakes
pka: 4.78±0.10(Predicted)
color: White or almost white
Odor: at 100.00 %. slightly waxy fatty
Odor Type: waxy
Water Solubility: insoluble
Merck: 14,6996
JECFA Number: 115
BRN: 607489
Dielectric constant: 2.3(71℃)
Stability: Stable. Combustible. Incompatible with bases, oxidizing agents, reducing agents.
InChIKey: IPCSVZSSVZVIGE-UHFFFAOYSA-N
LogP: 7.170
CAS DataBase Reference: 57-10-3(CAS DataBase Reference)
NIST Chemistry Reference: Palmitic Acid(57-10-3)
EPA Substance Registry System: Palmitic acid (57-10-3)

Uses
Palmitic Acid is one of the skin’s major fatty acids produced by the sebaceous glands.
In cosmetic preparations, Palmitic Acid is used as a formula texturizer.
Palmitic Acid is naturally occurring in allspice, anise, calamus oil, cascarilla bark, celery seed, coffee, tea, and many animal fats and plant oils.
Palmitic Acid is obtained from palm oil, Japan wax, or Chinese vegetable tallow.

Palmitic Acid is a common fatty acid found in plants and animals.
The body converts excess carbohydrates into Palmitic Acid, thus Palmitic Acid is the first fatty acid produced during fatty acid synt hesis as well as a precursor for longer fatty acids.
Palmitic Acid is a fatty acid which is a mixture of solid organic acids from fats consisting principally of palmitic acid with varying amounts of stearic acid.
Palmitic Acid functions as a lubricant, binder, and defoaming agent.
Palmitic acid is used in oral and topical pharmaceutical formulations.
Palmitic acid has been used in implants for sustained release of insulin in rats.

Excess carbohydrates in the body are converted to Palmitic Acid.
Palmitic acid is the first fatty acid produced during fatty acid synthesis and the precursor to longer fatty acids.
Palmitate negatively feeds back on acetyl-CoA carboxylase (ACC), which is responsible for converting acetyl-CoA to malonyl-CoA, which in turn is used to add to the growing acyl chain, thus preventing further palmitate generation.
In biology, some proteins are modified by the addition of a palmitoyl group in a process known as palmitoylation.
Palmitoylation is important for membrane localisation of many proteins.

Application
Palmitic acid is mainly used to produce soaps, cosmetics, and release agents.
These applications utilize sodium palmitate, which is commonly obtained by saponification of palm oil.
To this end, palm oil, rendered from the coconut palm nut, is treated with sodium hydroxide (in the form of caustic soda or lye), which causes hydrolysis of the ester groups. This procedure affords glycerol and sodium palmitate.
Because it is inexpensive and adds texture to processed foods (convenience food), palmitic acid and its sodium salt find wide use including foodstuffs.
Sodium palmitate is permitted as a natural additive in organic products.
Hydrogenation of palmitic acid yields cetyl alcohol, which is used to produce detergents and cosmetics.
Recently, a long-acting antipsychotic medication, paliperidone palmitate (marketed as INVEGA Sustenna), used in the treatment of schizophrenia, has been synthesized using the oily palmitate ester as a long-acting release carrier medium when injected intramuscularly.
The underlying method of drug delivery is similar to that used with decanoic acid to deliver long-acting depot medication, in particular, neuroleptics such as haloperidol decanoate.

Production Methods
Palmitic acid occurs naturally in all animal fats as the glyceride, palmitin, and in palm oil partly as the glyceride and partly uncombined.
Palmitic acid is most conveniently obtained from olive oil after removal of oleic acid, or from Japanese beeswax.
Synthetically, palmitic acid may be prepared by heating cetyl alcohol with soda lime to 270°C or by fusing oleic acid with potassium hydrate.

Purification Methods
Purify palmitic acid by slow (overnight) recrystallisation from hexane.
Some samples are also crystallised from acetone, EtOH or EtOAc.
The crystals are kept in air to lose solvent, or are pumped dry of solvent on a vacuum line.
PALMITIC ACID
Palmitic acid (hexadecanoic acid in IUPAC nomenclature) is a fatty acid with a 16-carbon chain.
Palmitic acid is the most common saturated fatty acid found in animals, plants and microorganisms.
Palmitic acid chemical formula is CH3(CH2)14COOH, and Palmitic acid C:D (the total number of carbon atoms to the number of carbon–carbon double bonds) is 16:0.

CAS Number: 57-10-3
EC Number: 200-312-9
Chemical Formula: CH3(CH2)14COOH
Molar Mass: 256.43 g/mol

Meats, cheeses, butter, and other dairy products also contain palmitic acid, amounting to 50–60% of total fats.
Palmitates are the salts and esters of palmitic acid.
The palmitate anion is the observed form of palmitic acid at physiologic pH (7.4).

Palmitic acid (PA), a saturated fatty acid present in the human body, accounts for 20-30% of total fatty acids (FA) in membrane phospholipids (PL) and adipose triacylglycerols (TAG).
Palmitic acid is one of the main components of palm oil however, significant amounts of Palmitic acid are also found in meat and dairy products, cocoa butter, and olive oil.

Palmitic acid is also present in breast milk.
Palmitic acid performs various fundamental biological functions at cellular and tissue levels.

Palmitic acid is a saturated long-chain fatty acid (LCFA), a term for fatty acids containing 13 to 21 carbons.
Palmitic acid contains 16 carbons.

This acid is found in most fats and oils, such as soybean oil.
Palmitic acid can also be found naturally in plants and animals and created in laboratories.
Additionally, palmitic acid can be found in foods such as palm oil, butter, meat, milk, and cheese.

Soybean oil is commonly found throughout human food and has many other applications as well.
One part of soybean oil is palmitic acid.
Many think that lowering the palmitic acid in soybean oil would reduce the fatty acid in the oil and increase the oil’s quality, making Palmitic acid better for humans to eat.

The palmitic acid structure contains a 16-carbon backbone.
The palmitic acid molecular formula contains C16H32O2, which is 16 carbon, 32 hydrogens, and 2 oxygen.

Palmitic acid has a molecular weight of 256.42.
Palmitic acid is commonly used in personal care products and cosmetics.

Palmitic acid has a bad reputation, primarily because Palmitic acid has been shown to have negative health effects.
Palmitic acid has been linked to several conditions, including brain diseases and cancer.

However, studies don't necessarily agree on this.
Associations between palmitic oil and an increased risk of breast cancer were found in one study but not in another, for example.

Palmitic acid can also be observed in Escherichia coli, or E. coli, and an aged mouse’s brain as a metabolite, which is a substance that deals with the metabolism.
The appearance of palmitic acid can be in a dry powder form, liquid, or other solid material.

Palmitic acid (hexadecanoic acid in IUPAC nomenclature) is a fatty acid with a 16-carbon chain.
Palmitic acid is the most common saturated fatty acid found in animals, plants and microorganisms.

Palmitic acid chemical formula is CH3(CH2)14COOH, and Palmitic acid C:D (the total number of carbon atoms to the number of carbon–carbon double bonds) is 16:0.
Palmitic acid is a major component of the oil from the fruit of oil palms (palm oil), making up to 44% of total fats.

Palmitic acid is often colorless with white crystalline scales.
Palmitic acid has a slight distinctive odor and taste but otherwise is odorless.

When heated and decayed, Palmitic acid gives off an acrid smoke.
The fumes from the smoke can be irritating.

As the first fatty acid to be produced during initial fatty acid synthesis, palmitic acid is a primary part of an animal’s body.
Additionally, in humans, palmitic acid has been seen to make up 21% to 30% of human depository fat.

Palmitic acid can be found in blood, cerebrospinal fluid (spinal tap fluid), feces, saliva, sweat, and urine, and also in tissues, including adipose tissue a.k.a. body fat, the bladder, skin, certain cells called fibroblasts, kidney, placenta, platelet, prostate, and skeletal muscle.
Palmitic acid is also known as hexadecanoic acid.

Palmitic Acid is a saturated long-chain fatty acid with a 16-carbon backbone.
Palmitic acid is found naturally in palm oil and palm kernel oil, as well as in butter, cheese, milk and meat.

Palmitic acid, or hexadecanoic acid is one of the most common saturated fatty acids found in animals and plants, a saturated fatty acid found in fats and waxes including olive oil, palm oil, and body lipids.
Palmitic acid occurs in the form of esters (glycerides) in oils and fats of vegetable and animal origin and is usually obtained from palm oil, which is widely distributed in plants.
Palmitic acid is used in determination of water hardness and is an active ingredient of Levovist, used in echo enhancement in sonographic Doppler B-mode imaging and as an ultrasound contrast medium.

Palmitic acid (PA) has been for long time negatively depicted for Palmitic acid putative detrimental health effects, shadowing Palmitic acid multiple crucial physiological activities.
Palmitic acid is the most common saturated fatty acid accounting for 20–30% of total fatty acids in the human body and can be provided in the diet or synthesized endogenously via de novo lipogenesis (DNL).
Palmitic acid tissue content seems to be controlled around a well-defined concentration, and changes in Palmitic acid intake do not influence significantly Palmitic acid tissue concentration because the exogenous source is counterbalanced by Palmitic acid endogenous biosynthesis.

Particular physiopathological conditions and nutritional factors may strongly induce DNL, resulting in increased tissue content of Palmitic acid and disrupted homeostatic control of Palmitic acid tissue concentration.
The tight homeostatic control of Palmitic acid tissue concentration is likely related to Palmitic acid fundamental physiological role to guarantee membrane physical properties but also to consent protein palmitoylation, palmitoylethanolamide (PEA) biosynthesis, and in the lung an efficient surfactant activity.

In order to maintain membrane phospholipids (PL) balance may be crucial an optimal intake of Palmitic acid in a certain ratio with unsaturated fatty acids, especially PUFAs of both n-6 and n-3 families.
However, in presence of other factors such as positive energy balance, excessive intake of carbohydrates (in particular mono and disaccharides), and a sedentary lifestyle, the mechanisms to maintain a steady state of Palmitic acid concentration may be disrupted leading to an over accumulation of tissue.

Palmitic acid resulting in dyslipidemia, hyperglycemia, increased ectopic fat accumulation and increased inflammatory tone via toll-like receptor 4.
Palmitic acid is therefore likely that the controversial data on the association of dietary Palmitic acid with detrimental health effects, may be related to an excessive imbalance of dietary PA/PUFA ratio which, in certain physiopathological conditions, and in presence of an enhanced DNL, may further accelerate these deleterious effects.

Palmitic acid is used to produce soaps, cosmetics, and industrial mold release agents.
These applications use sodium palmitate, which is commonly obtained by saponification of palm oil.

To this end, palm oil, rendered from palm tree (species Elaeis guineensis), is treated with sodium hydroxide, which causes hydrolysis of the ester groups, yielding glycerol and sodium palmitate.
Hydrogenation of palmitic acid yields cetyl alcohol, which is used to produce detergents and cosmetics

Topical palmitic acid is not known to cause side effects.
A diet containing large amounts of palmitic acid can increase risk of heart disease but topical application doesn’t contribute to this.

Palmitic acid strongly boosts metastasis in mouse models of human oral cancer cells.
Among all fatty acids, Palmitic Acid has the strongest effect in boosting the metastatic potential of CD36+ metastasis-initiating cells.

Palmitic AcidPalmitic acid is a saturated fatty acid commonly found in both animals and plants.
Palmitic Acid is a major component in the oils from palm trees, such as palm oil, palm kernel oil and coconut oil.
Palmitic acid, a kind of fatty acid, derived from palm oil.

Palmitic Acid is a major component in the oils from palm trees.
Applications of palmitic acid include soap & detergent, cosmetics, grease & lubricant, etc.
Among those applications, soap & detergent accounts for the largest market share, which was about 49.99% in 2016.

The palmitic acid industry production is mainly concentrated in Asian region, such as Malaysia, Indonesia, China and so on.
The largest producing region is Southeast Asia, which produced 135373 MT in 2016.

The follower is China, holding 18.50% production share.
Global production of palmitic acid increased from 166874 MT in 2012 to 202753 MT in 2016.

As for consumption, Europe is the largest consumer with about 33.51% share in 2016.
The second consumer is China, consuming 57456 MT in the same year.

The palmitic acid industry has close relationship with the palm oil industry.
Due to Palmitic Acid low profit, some companies engaged in the palm oil industry have given up the business.
In China, there are just a few suppliers.

The Palmitic Acid Industry Report indicates that the global market size of Palmitic Acid was XX USD in 2020, and will grow at a XX% CAGR between 2021 and 2027.

A collective analysis on ’Palmitic Acid Industry’ offers an exhaustive study supported current trends influencing this vertical throughout assorted geographies.
Key information regarding market size, market share, statistics, application, and revenue is within the research to develop an ensemble prediction.
Additionally, this research offers an in-depth competitive analysis that specializes in business outlook emphasizing expansion strategies accepted by Palmitic Acid market majors.

Palmitic acid is a saturated fatty acid, the principal constituent of refined palm oil, present in the diet and synthesized endogenously.
Palmitic acid is able to activate the orphan G protein-coupled receptor GPR40.

Palmitic acid was also a weak ligand of peroxisome proliferator-activated receptor gamma.
Palmitic acid is a ligand of lipid chaperones - the fatty acid-binding proteins (FABPs).
Dietary palm oil and palmitic acid may play a role in the development of obesity, type 2 diabetes mellitus, cardiovascular diseases and cancer

Palmitic acid is a saturated fatty acid that occurs in natural fats and oils, tall oil, and most commercial grade stearic acid.
Palmitic acid is prepared by treating fats and oils with water at a high pressure and temperature, leading to the hydrolysis of triglycerides.

Palmitic acid is mainly usedin the manufacture of metallic palmitates, soaps, cosmetics, lubricating oils, waterproofing release agents, and in food-grade additives.

Palmitic acid is a long-chain saturated fatty acid commonly found in both animals and plants.
Palmitic acid is a white, crystalline, water-insoluble solid, C16H32O2, obtained by hydrolysis from palm oil and natural fats, in which Palmitic Acid occurs as the glyceride, and from spermaceti: used in the manufacture of soap.
Palmitic acid can induce the expression of glucose-regulated protein 78 (GRP78) and CCAAT/enhancer binding protein homologous protein (CHOP) in in mouse granulosa cells.

Applications of Palmitic acid:

Palmitic acid has been used:
To study Palmitic acid effects on monocyte chemoattractant protein-1 (MCP-1) expression in adipocytes and THP-1 macrophages
To stimulate lipotoxicity in primary rat hepatocytes
In Et-bovine serum albumin (BSA) solution along with retinoic acid (RA) and retinol to study Palmitic acid effects on spermatogenesis or meiotic progression

Surfactant:
Palmitic acid is used to produce soaps, cosmetics, and industrial mold release agents.
These applications use sodium palmitate, which is commonly obtained by saponification of palm oil.
To this end, palm oil, rendered from palm tree (species Elaeis guineensis), is treated with sodium hydroxide (in the form of caustic soda or lye), which causes hydrolysis of the ester groups, yielding glycerol and sodium palmitate.

Foods:
Because Palmitic acid is inexpensive and adds texture and "mouthfeel" to processed foods (convenience food), palmitic acid and Palmitic acid sodium salt find wide use in foodstuffs.
Sodium palmitate is permitted as a natural additive in organic products.

Military:
Aluminium salts of palmitic acid and naphthenic acid were the gelling agents used with volatile petrochemicals during World War II to produce napalm.
The word "napalm" is derived from the words naphthenic acid and palmitic acid.

Schizophrenia:
Recently, a long-acting antipsychotic medication, paliperidone palmitate (marketed as INVEGA Sustenna), used in the treatment of schizophrenia, has been synthesized using the oily palmitate ester as a long-acting release carrier medium when injected intramuscularly.
The underlying method of drug delivery is similar to that used with decanoic acid to deliver long-acting depot medication, in particular, neuroleptics such as haloperidol decanoate.

Health effects:
According to the World Health Organization, evidence is "convincing" that consumption of palmitic acid increases the risk of developing cardiovascular disease, based on studies indicating that Palmitic Acid may increase LDL levels in the blood.
Retinyl palmitate is a source of vitamin A added to low-fat milk to replace the vitamin content lost through the removal of milk fat.
Palmitate is attached to the alcohol form of vitamin A, retinol, to make vitamin A stable in milk.

Uses of Palmitic acid:
Palmitic acid has several uses.
For example, Palmitic acid can be used to test the hardness in water and is a part of the intravenous ultrasonic contrast agent Levovist, which is used during ultrasounds to detect certain diseases.

Palmitic acid can promote smooth skin, so Palmitic acid’s found in many soaps.
Additionally, the popular ingredient beeswax, often found in personal care items, also houses palmitic acid.
Cosmetic-wise, palmitic acid can be found in makeup used to hide imperfections such as pimples and blackheads.

Another common use for palmitic acid is in cleaning products, typically surface-active agents, such as detergent.
Palmitic acid is also used when making metallic palmitates, food-grade additives, and lube oils.

Palmitic acid is found as glycerol ester in oils and fats.
Palmitic acid is produced from palm oil, Japan wax, or Chinese vegetable tallow.

Palmitic acid is very common naturally occurring fatty acid.
Palmitic acid is used to make metallic palmitates and esters.
Palmitic acid is used in soaps and cosmetics; in lube oils; for waterproofing; in food-grade additives; as a non-drying oil (surface coating).

Palmitic acid is used in manufacture of metallic palmitates, soaps, lubricating oils, waterproofing, food-grade additives.

This is an endogenously produced metabolite found in the human body.
Palmitic acid is used in metabolic reactions, catabolic reactions or waste generation.

Industry Uses:
Adhesives and sealant chemicals
Agricultural chemicals (non-pesticidal)
Anti-freeze agent
Emulsifier
Finishing agents
Fuel
Intermediate
Intermediates
Lubricants and lubricant additives
Lubricating agent
Not Known or Reasonably Ascertainable
Opacifer
Polymerization promoter
Processing aids not otherwise specified
Stabilizing agent
Surface active agents
Surface modifier
Surfactant (surface active agent)
Viscosity modifiers

Consumer Uses:
Adhesives and sealant chemicals
Agricultural chemicals (non-pesticidal)
Emulsifier
Hardener
Lubricants and lubricant additives
Lubricating agent
Not Known or Reasonably Ascertainable
Opacifer
Surface modifier
Surfactant (surface active agent)
Viscosity adjustors

Industrial Processes with risk of exposure:
Painting (Pigments, Binders, and Biocides)

Dietary Sources of Palmitic acid:
Palmitic acid is produced by a wide range of other plants and organisms, typically at low levels.
Palmitic acid is present in butter, cheese, milk, and meat, as well as cocoa butter, olive oil, soybean oil, and sunflower oil.

Karukas contain 44.90% palmitic acid.
The cetyl ester of palmitic acid (cetyl palmitate) occurs in spermaceti.

Structure and Properties of Palmitic Acid:
Palmitic acid is a saturated fatty acid (no double bond so in shorthand 16:0) member of the sub-group called long chain fatty acids (LCFA), from 14 to 18 carbon atoms.

Palmitic Acid is the first fatty acid produced during fatty acid synthesis in humans and the fatty acid from which longer fatty acids can be produced.

Palmitic acid was discovered by Edmond Frémy in 1840, in saponified palm oil.
This remains the primary industrial route for Palmitic Acid production, with the triglycerides (fats) in palm oil being hydrolysed by high temperature water (above 200 °C or 390 °F), and the resulting mixture fractionally distilled to give the pure product.

As a consequence, palmitic acid is a major body component of animals.
In humans, one analysis found Palmitic Acid to make up 21–30% (molar) of human depot fat, and Palmitic Acid is a major, but highly variable, lipid component of human breast milk.
Palmitate negatively feeds back on acetyl-CoA carboxylase (ACC), which is responsible for converting acetyl-CoA to malonyl-CoA, which in turn is used to add to the growing acyl chain, thus preventing further palmitate generation

One of the main functions of palmitic acid alkali salts is that they acts as emulsifiers and surfactants, allowing oil based, hydrophobic molecules to interact with water where normally they would repel each other.
This works by the fatty acid end of the salt interacting with the oil while the salt end interacts with the water creating an adapter between oil and water.

In some products this increases the stability of the product as oil and water would naturally separate without Palmitic Acid.
In soaps and cleansing oils, the fatty end grabs oil and water-resistant make up on your skin while the salt end then lets water wash everything off.

Occurrence and Production of Palmitic acid:
Palmitic acid was discovered by Edmond Frémy in 1840, in saponified palm oil.
This remains the primary industrial route for Palmitic acid production, with the triglycerides (fats) in palm oil being hydrolysed by high-temperature water, and the resulting mixture fractionally distilled.

Biochemistry of Palmitic acid:
Palmitic acid is the first fatty acid produced during fatty acid synthesis and is the precursor to longer fatty acids.
As a consequence, palmitic acid is a major body component of animals.

In humans, one analysis found Palmitic acid to make up 21–30% (molar) of human depot fat, and Palmitic acid is a major, but highly variable, lipid component of human breast milk.
Palmitate negatively feeds back on acetyl-CoA carboxylase (ACC), which is responsible for converting acetyl-CoA to malonyl-CoA, which in turn is used to add to the growing acyl chain, thus preventing further palmitate generation.

Some proteins are modified by the addition of a palmitoyl group in a process known as palmitoylation.
Palmitoylation is important for localisation of many membrane proteins.

Research of Palmitic acid:
Palmitic acid is well accepted in the medical community that palmitic acid from dietary sources raises low-density lipoprotein (LDL) and total cholesterol.
The World Health Organization have stated there is convincing evidence that palmitic acid increases cardiovascular disease risk.

A 2021 review indicated that replacing dietary palmitic acid and other saturated fatty acids with unsaturated fatty acids, such as oleic acid, could reduce several biomarkers of cardiovascular and metabolic diseases.

Pharmacology and Biochemistry of Palmitic acid:

Pharmacodynamics:
Palmitic acid is the first fatty acid produced during lipogenesis (fatty acid synthesis) and from which longer fatty acids can be produced.
Palmitate negatively feeds back on acetyl-CoA carboxylase (ACC) which is responsible for converting acetyl-ACP to malonyl-ACP on the growing acyl chain, thus preventing further palmitate generation

MeSH Pharmacological Classification of Palmitic acid:

Enzyme Inhibitors:
Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction.

Bionecessity:
Palmitic acid is required for biosynthesis of lung lecithin, which is related to fetal maturation.
Radiochromatogram showed high incorporation of palmitate into lecithin by fetal lung.
Content in palm oil in Nigerian meals can partly be related to low incidence of respiratory distress.

Palmitic acid is a saturated fatty acid present in the diet and synthesized endogenously.
Although often considered to have adverse effects on chronic disease in adults, Palmitic acid is an essential component of membrane, secretory, and transport lipids, with crucial roles in protein palmitoylation and signal molecules.

At birth, the term infant is 13-15% body fat, with 45-50% Palmitic acid, much of which is derived from endogenous synthesis in the fetus.
After birth, the infant accumulates adipose tissue at high rates, reaching 25% body weight as fat by 4-5 months age.

Over this time, human milk provides 10% dietary energy as Palmitic acid, but in unusual triglycerides with Palmitic acid on the glycerol center carbon.
This paper reviews the synthesis and oxidation of Palmitic acid and possible reasons why the infant is endowed with large amounts of fat and Palmitic acid.

The marked deviations in tissues with displacement of Palmitic acid that can occur in infants fed vegetable oil formulas is introduced.
Assuming fetal fatty acid synthesis and the unusual delivery of Palmitic acid in human milk evolved to afford survival advantage to the neonate, Palmitic acid is timely to question if Palmitic acid is an essential component of tissue lipids whereby both deficiency and excess are detrimental.

Absorption, Distribution and Excretion of Palmitic acid:
Added (14)C-labeled palmitate was more significantly incorporated into lipid fractions of muscle fibers from fetal and neonatal monkeys than those from adults.

More (14)C-labeled palmitate was incorporated into lipid by adipose tissue of genetically obese rats than by controls.
Radioactivity has been traced to the heart, liver, lung, spleen, kidney, muscle, intestine, adrenal, blood, and lymph, and adipose, mucosal, and dental tissues after administration of radioactive oleic, palmitic, or stearic acids.

Fatty acids originating from adipose tissue stores are either bound to serum albumin or remain unesterified in the blood.

Human Metabolite Information of Palmitic acid:

Tissue Locations:
Adipose Tissue
Bladder
Epidermis
Fibroblasts
Kidney
Placenta
Platelet
Prostate
Skeletal Muscle

Cellular Locations:
Cytoplasm
Endoplasmic reticulum
Extracellular
Membrane
Peroxisome

General Manufacturing Information of Palmitic acid:

Industry Processing Sectors:
Adhesive Manufacturing
All Other Basic Organic Chemical Manufacturing
Construction
Fabricated Metal Product Manufacturing
Food, beverage, and tobacco product manufacturing
Machinery Manufacturing
Miscellaneous Manufacturing
Not Known or Reasonably Ascertainable
Other (requires additional information)
Paint and Coating Manufacturing
Paper Manufacturing
Petroleum Lubricating Oil and Grease Manufacturing
Plastics Material and Resin Manufacturing
Plastics Product Manufacturing
Rubber Product Manufacturing
Soap, Cleaning Compound, and Toilet Preparation Manufacturing
Textiles, apparel, and leather manufacturing
Wholesale and Retail Trade

Handling and Storage of Palmitic acid:

Safe Storage:
Separated from bases, oxidants and reducing agents.

Storage Conditions:
Keep container tightly closed in a dry and well-ventilated place.
Storage class (TRGS 510): Non Combustible Solids

Accidental Release Measures of Palmitic acid:

Spillage Disposal:
Sweep spilled substance into covered containers.
If appropriate, moisten first to prevent dusting.

Cleanup Methods of Palmitic acid:

Personal precautions, protective equipment and emergency procedures:
Avoid dust formation.
Avoid breathing vapors, mist or gas.

Environmental precautions:
No special environmental precautions required.

Methods and materials for containment and cleaning up:
Sweep up and shovel.
Keep in suitable, closed containers for disposal.

Disposal Methods of Palmitic acid:
Recycle any unused portion of the material for Palmitic acid approved use or return it to the manufacturer or supplier.

Ultimate disposal of the chemical must consider:
Palmitic acid's impact on air quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations.
If Palmitic acid is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.

Offer surplus and non-recyclable solutions to a licensed disposal company.

Contaminated packaging:
Dispose of as unused product

Preventive Measures of Palmitic acid:

Personal precautions, protective equipment and emergency procedures:
Avoid dust formation.
Avoid breathing vapors, mist or gas.

Gloves must be inspected prior to use.
Use proper glove removal technique (without touching glove's outer surface) to avoid skin contact with this product.

Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Further processing of solid materials may result in the formation of combustible dusts.
The potential for combustible dust formation should be taken into consideration before additional processing occurs.

Provide appropriate exhaust ventilation at places where dust is formed.
Local exhaust ventilation should be applied wherever there is an incidence of point source emissions or dispersion of regulated contaminants in the work area.

Ventilation control of the contaminant as close to Palmitic acid point of generation is both the most economical and safest method to minimize personnel exposure to airborne contaminants.
Ensure that the local ventilation moves the contaminant away from the worker.

The scientific literature for the use of contact lenses by industrial workers is inconsistent.
The benefits or detrimental effects of wearing contact lenses depend not only upon Palmitic acid, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses.
However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye.

In those specific cases, contact lenses should not be worn.
In any event, the usual eye protection equipment should be worn even when contact lenses are in place.

Identifiers of Palmitic acid:
CAS Number: 57-10-3
ChEMBL: ChEMBL82293
ChemSpider: 960
ECHA InfoCard: 100.000.284
IUPHAR/BPS: 1055
PubChem CID: 985
UNII: 2V16EO95H1
CompTox Dashboard (EPA): DTXSID2021602
InChI:MInChI=1S/C16H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-15H2,1H3,(H,17,18)
Key: IPCSVZSSVZVIGE-UHFFFAOYSA-N
InChI=1/C16H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-15H2,1H3,(H,17,18)
Key: IPCSVZSSVZVIGE-UHFFFAOYAJ
SMILES: CCCCCCCCCCCCCCCC(=O)O

Synonym(s): 1-Pentadecanecarboxylic acid, C16:0, Cetylic acid, Hexadecanoic acid, NSC 5030, PamOH
Linear Formula: CH3(CH2)14COOH
CAS Number: 57-10-3
Molecular Weight: 256.42
Beilstein: 607489
EC Number: 200-312-9
MDL number: MFCD00002747
PubChem Substance ID: 24898107
NACRES: NA.25

CAS number: 57-10-3
EC number: 200-312-9
Hill Formula: C₁₆H₃₂O₂
Chemical formula: CH₃(CH₂)₁₄COOH
Molar Mass: 256.43 g/mol
HS Code: 2915 70 40

Properties of Palmitic acid:
Chemical formula: C16H32O2
Molar mass: 256.430 g/mol
Appearance: White crystals
Density: 0.852 g/cm3 (25 °C)
0.8527 g/cm3 (62 °C)[3]
Melting point: 62.9 °C (145.2 °F; 336.0 K)
Boiling point: 351–352 °C (664–666 °F; 624–625 K)
271.5 °C (520.7 °F; 544.6 K), 100 mmHg
215 °C (419 °F; 488 K), 15 mmHg
Solubility in water: 4.6 mg/L (0 °C)
7.2 mg/L (20 °C)
8.3 mg/L (30 °C)
10 mg/L (45 °C)
12 mg/L (60 °C)
Solubility: Soluble in amyl acetate, alcohol, CCl4, C6H6
Very soluble in CHCl3
Solubility in ethanol: 2 g/100 mL (0 °C)
2.8 g/100 mL (10 °C)
9.2 g/100 mL (20 °C)
31.9 g/100 mL (40 °C)
Solubility in methyl acetate: 7.81 g/100 g
Solubility in ethyl acetate: 10.7 g/100 g
Vapor pressure: 0.051 mPa (25 °C)
1.08 kPa (200 °C)
28.06 kPa (300 °C)
Acidity (pKa): 4.75
Magnetic susceptibility (χ): −198.6·10−6 cm3/mol
Refractive index (nD): 1.43 (70 °C)
Viscosity: 7.8 cP (70 °C)

Boiling point: 271.4 °C (133 hPa)
Density: 0.852 g/cm3
Flash point: 113 °C
Melting Point: 60 - 65 °C
Vapor pressure: 13 hPa (210 °C)
Bulk density: 415 kg/m3

Vapor pressure: 10 mmHg ( 210 °C)
Quality Level: 200
Assay: ≥99%
Form: powder
bp: 271.5 °C/100 mmHg (lit.)
mp: 61-62.5 °C (lit.)
Density: 0.852 g/mL at 25 °C (lit.)
Functional group: carboxylic acid
Shipped in: ambient
Storage temp.: room temp
SMILES string: CCCCCCCCCCCCCCCC(O)=O
InChI: 1S/C16H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-15H2,1H3,(H,17,18)
InChI key: IPCSVZSSVZVIGE-UHFFFAOYSA-N

Molecular Weight: 256.42
XLogP3: 6.4
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 14
Exact Mass: 256.240230259
Monoisotopic Mass: 256.240230259
Topological Polar Surface Area: 37.3 Ų
Heavy Atom Count: 18
Complexity: 178
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Specifications of Palmitic acid:
Assay (GC, area%): ≥ 98.0 % (a/a)
Melting range (lower value): ≥ 62 °C
Melting range (upper value): ≤ 64 °C
Identity (IR): passes test

Thermochemistry of Palmitic acid:
Heat capacity (C): 463.36 J/(mol·K)[6]
Std molar entropy (S⦵298): 452.37 J/(mol·K)
Std enthalpy of formation (ΔfH⦵298): −892 kJ/mol
Std enthalpy of combustion (ΔcH⦵298): 10030.6 kJ/mol

Names of Palmitic Acid:

CAS names:
Hexadecanoic acid

IUPAC names:
Hexadecanoic acid
hexadecanoic acid
PALMITIC ACID
Palmitic Acid

Trade names:
CREMERAC
KORTACID 1698/1695/1690
MASCID 1680
MASCID 1698
PALMAC 80-16, Palmitic Acid 80% Min.
PALMAC 95-16, Palmitic Acid 95% Min.
PALMAC 98-16, Palmitic Acid 98% Min.
Palmata 1698
PALMERA A8016
PALMERA A9216
PALMERA A9516
PALMERA A9816
Palmitic Acid
RADIACID 0656
RADIACID 0657
RADIACID 0658
Tefacid Palmitic 92
Tefacid Palmitic 98

Preferred IUPAC names:
Hexadecanoic acid
C16:0 (Lipid numbers)

Other names:
Hexadecanoic acid
n-Hexadecoic acid
Palmitic acid
Pentadecanecarboxylic acid
1-Pentadecanecarboxylic acid
Cetylic acid
Emersol 140
Emersol 143
Hexadecylic acid
Hydrofol
Hystrene 8016
Hystrene 9016
Industrene 4516
Glycon P-45
Prifac 2960
NSC 5030
Palmitinic acid
Kortacid 1695
60605-23-4
116860-99-2
212625-86-0
Hexadecanoic acid (palmitic acid)
Hexadecanoic (palmitic) acid
Palmitic acid (hexadecanoic acid)

Synonyms of Palmitic acid:
palmitic acid
Hexadecanoic acid
57-10-3
Cetylic acid
palmitate
n-Hexadecanoic acid
Hexadecylic acid
Hydrofol
n-Hexadecoic acid
1-Pentadecanecarboxylic acid
Palmitinic acid
Pentadecanecarboxylic acid
hexadecanoate
hexaectylic acid
1-Hexyldecanoic Acid
hexadecoic acid
Industrene 4516
Emersol 140
Emersol 143
Hystrene 8016
Hystrene 9016
Palmitinsaeure
Palmitic acid, pure
FEMA No. 2832
Palmitic acid 95%
Kortacid 1698
Loxiol EP 278
Palmitic acid (natural)
Hydrofol Acid 1690
Prifac 2960
Pristerene 4934
Edenor C16
Lunac P 95KC
C16:0
Lunac P 95
Lunac P 98
Cetyl acid
HSDB 5001
AI3-01594
NSC 5030
Pristerene-4934
Palmitic acid (NF)
Glycon P-45
CHEBI:15756
NSC5030
Prifac-2960
NSC-5030
Hexadecanoic acid (9CI)
MFCD00002747
Palmitic acid (7CI,8CI)
CHEMBL82293
CH3-[CH2]14-COOH
IMEX C 1498
2V16EO95H1
n-hexadecoate
LMFA01010001
PA 900
67701-02-4
FA 16:0
FA 1695
1-hexyldecanoate
NCGC00164358-01
pentadecanecarboxylate
Hexadecanoic acid 10 microg/mL in Acetonitrile
C16H32O2
PLM
palmic acid
Hexadecanoate (n-C16:0)
CAS-57-10-3
CCRIS 5443
SR-01000944716
EINECS 200-312-9
Palmitic acid [USAN:NF]
BRN 0607489
palmitoate
Hexadecoate
Palmitinate
palmitic-acid
palmitoic acid
Hexadecanoicacid
Aethalic acid
UNII-2V16EO95H1
Hexadecanoic acid Palmitic acid
2hmb
2hnx
Palmitic acid_jeyam
Palmitic Acid, FCC
Kortacid 1695
Palmitic acid_RaGuSa
Univol U332
Prifrac 2960
Hexadecanoic acid anion
3v2q
Palmitic acid, >=99%
bmse000590
Epitope ID:141181
EC 200-312-9
CETYL ACID [VANDF]
PALMITIC ACID [II]
PALMITIC ACID [MI]
SCHEMBL6177
PALMITIC ACID [DSC]
PALMITIC ACID [FCC]
PALMITIC ACID [FHFI]
PALMITIC ACID [HSDB]
PALMITIC ACID [INCI]
PALMITIC ACID [USAN]
4-02-00-01157 (Beilstein Handbook Reference)
FAT
WLN: QV15
P5585_SIGMA
PALMITIC ACID [VANDF]
PALMITIC ACID [MART.]
GTPL1055
QSPL 166
PALMITIC ACID [USP-RS]
PALMITIC ACID [WHO-DD]
(1(1)(3)C)hexadecanoic acid
DTXSID2021602
1b56
HMS3649N08
Palmitic acid, analytical standard
Palmitic acid, BioXtra, >=99%
Palmitic acid, Grade II, ~95%
HY-N0830
Palmitic acid, natural, 98%, FG
ZINC6072466
Tox21_112105
Tox21_201671
Tox21_302966
AC9381
BBL011563
BDBM50152850
PALMITIC ACID [EP MONOGRAPH]
s3794
STL146733
EDENOR C 16-98-100
Palmitic acid, >=95%, FCC, FG
AKOS005720983
Tox21_112105_1
CCG-267027
CR-0047
DB03796
Palmitic acid, for synthesis, 98.0%
SURFAXIN COMPONENT PALMITIC ACID
NCGC00164358-02
NCGC00164358-03
NCGC00256424-01
NCGC00259220-01
BP-27917
LUCINACTANT COMPONENT PALMITIC ACID
Palmitic acid, purum, >=98.0% (GC)
SY006518
CS-0009861
FT-0626965
FT-0772579
P0002
P1145
Palmitic acid, SAJ first grade, >=95.0%
EN300-19603
A14813
C00249
D05341
Palmitic acid, Vetec(TM) reagent grade, 98%
Palmitic acid, >=98% palmitic acid basis (GC)
A831313
HEXADECANOIC ACID-13C16 (ALGAL SOURCE) (
Q209727
SR-01000944716-1
SR-01000944716-2
BA71C79B-C9B1-451A-A5BE-B480B5CC7D0C
PALMITIC ACID (CONSTITUENT OF SPIRULINA) [DSC]
F0001-1488
Z104474418
PALMITIC ACID (CONSTITUENT OF SAW PALMETTO) [DSC]
Palmitic acid, certified reference material, TraceCERT(R)
Palmitic acid, European Pharmacopoeia (EP) Reference Standard
Palmitic acid, United States Pharmacopeia (USP) Reference Standard
Palmitic acid, Pharmaceutical Secondary Standard; Certified Reference Material
Sodium Palmitate, Palmitic acid sodium salt, Sodium hexadecanoate, Sodium pentadecanecarboxylate, HSDB 759
PALMITIC ACID (HEXADECANOIC ACID)
Palmitic acid (hexadecanoic acid) is a straight-chain, sixteen-carbon, saturated long-chain fatty acid.
Palmitic acid (hexadecanoic acid) is a saturated long-chain fatty acid with a 16-carbon backbone.


CAS Number: 57-10-3
EC Number: 200-312-9
Chemical formula: C16H32O2


Palmitic acid (hexadecanoic acid) is a straight-chain, sixteen-carbon, saturated long-chain fatty acid.
Palmitic acid (hexadecanoic acid) has a role as an EC 1.1.1.189 (prostaglandin-E2 9-reductase) inhibitor, a plant metabolite, a Daphnia magna metabolite and an algal metabolite.


Palmitic acid (hexadecanoic acid) is a long-chain fatty acid and a straight-chain saturated fatty acid.
Palmitic acid (hexadecanoic acid) is a conjugate acid of a hexadecanoate.
A common saturated fatty acid, Palmitic acid (hexadecanoic acid), is found in fats and waxes including olive oil, palm oil, and body lipids.


Palmitic acid (hexadecanoic acid) is a metabolite found in or produced by Escherichia coli.
Palmitic acid (hexadecanoic acid) is a saturated long-chain fatty acid with a 16-carbon backbone.
Palmitic acid (hexadecanoic acid) is found naturally in palm oil and palm kernel oil, as well as in butter, cheese, milk and meat.


Palmitic acid (hexadecanoic acid) is one of the most common saturated fatty acids found in animals and plants, a saturated fatty acid found in fats and waxes including olive oil, palm oil, and body lipids.
Palmitic acid (hexadecanoic acid) occurs in the form of esters (glycerides) in oils and fats of vegetable and animal origin and is usually obtained from palm oil, which is widely distributed in plants.


Palmitic acid (hexadecanoic acid) is used in determination of water hardness and is an active ingredient of *Levovist*TM, used in echo enhancement in sonographic Doppler B-mode imaging and as an ultrasound contrast medium.
Palmitic acid (hexadecanoic acid) is a fatty acid with a 16-carbon chain.


Palmitic acid (hexadecanoic acid) is the most common saturated fatty acid found in animals, plants and microorganisms.
Palmitic acid (hexadecanoic acid)'s chemical formula is CH3(CH2)14COOH, and its C:D (the total number of carbon atoms to the number of carbon–carbon double bonds) is 16:0.


Palmitic acid (hexadecanoic acid) is a major component of the oil from the fruit of oil palms (palm oil), making up to 44% of total fats.
Meats, cheeses, butter, and other dairy products also contain Palmitic acid (hexadecanoic acid), amounting to 50–60% of total fats.
Palmitates are the salts and esters of palmitic acid.


The palmitate anion is the observed form of palmitic acid at physiologic pH (7.4).
Major sources of C16:0 are palm oil, palm kernel oil, coconut oil, and milk fat.
Palmitic acid (hexadecanoic acid) is one of the most common saturated fatty acids found in animals, plants, and microorganisms.


As its name indicates, Palmitic acid (hexadecanoic acid) is a major component of the oil from the fruit of oil palms (palm oil).
Excess carbohydrates in the body are converted to Palmitic acid (hexadecanoic acid).
Palmitic acid (hexadecanoic acid) is the first fatty acid produced during fatty acid synthesis and is the precursor to longer fatty acids.


As a consequence, Palmitic acid (hexadecanoic acid) is a major body component of animals.
In humans, one analysis found Palmitic acid (hexadecanoic acid) to make up 21–30% (molar) of human depot fat, and it is a major, but highly variable, lipid component of human breast milk.


To this end, palm oil, rendered from palm tree (species Elaeis guineensis), is treated with sodium hydroxide (in the form of caustic soda or lye), which causes hydrolysis of the ester groups, yielding glycerol and sodium palmitate.
Aluminium salts of Palmitic acid (hexadecanoic acid) and naphthenic acid were combined during World War II to produce napalm.


The word "napalm" is derived from the words naphthenic acid and Palmitic acid (hexadecanoic acid).
Palmitic acid (hexadecanoic acid) is also used in the determination of water hardness and is a surfactant of Levovist, an intravenous ultrasonic contrast agent.


Palmitic acid (hexadecanoic acid) is a saturated long-chain fatty acid (LCFA), a term for fatty acids containing 13 to 21 carbons.
Palmitic acid (hexadecanoic acid) contains 16 carbons.
Palmitic acid (hexadecanoic acid) is found in most fats and oils, such as soybean oil.


Palmitic acid (hexadecanoic acid) can also be found naturally in plants and animals and created in laboratories.
Additionally, Palmitic acid (hexadecanoic acid) can be found in foods such as palm oil, butter, meat, milk, and cheese.
Soybean oil is commonly found throughout human food and has many other applications as well.


One part of soybean oil is Palmitic acid (hexadecanoic acid).
Many think that lowering the palmitic acid in soybean oil would reduce the fatty acid in the oil and increase the oil’s quality, making it better for humans to eat.


Palmitic acid (hexadecanoic acid) structure contains a 16-carbon backbone.
Palmitic acid (hexadecanoic acid) molecular formula contains C16H32O2, which is 16 carbon, 32 hydrogens, and 2 oxygen.
Palmitic acid (hexadecanoic acid) has a molecular weight of 256.42.


The appearance of Palmitic acid (hexadecanoic acid) can be in a dry powder form, liquid, or other solid material.
Palmitic acid (hexadecanoic acid) is often colorless with white crystalline scales.
Palmitic acid (hexadecanoic acid) has a slight distinctive odor and taste but otherwise is odorless.


When heated and decayed, Palmitic acid (hexadecanoic acid) gives off an acrid smoke.
As the first fatty acid to be produced during initial fatty acid synthesis, Palmitic acid (hexadecanoic acid) is a primary part of an animal’s body.
Additionally, in humans, Palmitic acid (hexadecanoic acid) has been seen to make up 21% to 30% of human depository fat.


Palmitic acid (hexadecanoic acid) can be found in blood, cerebrospinal fluid (spinal tap fluid), feces, saliva, sweat, and urine, and also in tissues, including adipose tissue a.k.a. body fat, the bladder, skin, certain cells called fibroblasts, kidney, placenta, platelet, prostate, and skeletal muscle.
Palmitic acid (hexadecanoic acid), also known as palmitate or C16, belongs to the class of organic compounds known as long-chain fatty acids.


These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.
Palmitic acid (hexadecanoic acid) is a very hydrophobic molecule, practically insoluble in water and relatively neutral.
Palmitic acid (hexadecanoic acid) is one of the most common saturated fatty acids found in animals, plants, and microorganisms.


As its name indicates, Palmitic acid (hexadecanoic acid) is a major component of the oil from the fruit of oil palms (palm oil).
In humans and other mammals, excess carbohydrates in the body are converted to Palmitic acid (hexadecanoic acid).
Palmitic acid (hexadecanoic acid) is the first fatty acid produced during fatty acid synthesis and is the precursor to longer fatty acids.


As a consequence, Palmitic acid (hexadecanoic acid) is a major lipid component of animals.
In humans, one analysis found Palmitic acid (hexadecanoic acid) to make up 21–30% (molar) of human depot fat (PMID: 13756126), and it is a major, but highly variable, lipid component of human breast milk (PMID: 352132).


Palmitic acid (hexadecanoic acid) has been detected, but not quantified in, several different foods, such as sea-buckthornberries, avocado, star fruits, babassu palms, and acerola.
Palmitic acid (hexadecanoic acid) belongs to the class of organic compounds known as long-chain fatty acids.


These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.
Palmitic acid (hexadecanoic acid) is available in liquid or solid (bead or flake) forms.
Palmitic acid (hexadecanoic acid) has a light odor and a white or pale appearance, and it can last for up two years when stored according to instructions in the product MSDS (one year in its liquid form).


Palmitic acid (hexadecanoic acid), also known as C16 or hexadecanoate, belongs to the class of organic compounds known as long-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.
Palmitic acid (hexadecanoic acid) is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.


Palmitic acid (hexadecanoic acid) is a naturally occurring fatty acid found in animal and plant lipids.
Palmitic acid (hexadecanoic acid) is a white glossy solid and a major component of the oil derived from palm kernels.
This saturated fatty acid, Palmitic acid (hexadecanoic acid), occurs naturally in the fats of many animals, plants and microorganisms; and can also be found in butter, cheese, milk, meat, sunflower oil and soybean oil.


Palmitic acid (hexadecanoic acid) belongs to the class of organic compounds known as long-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.
Palmitic acid (hexadecanoic acid) is the first fatty acid produced during lipogenesis (fatty acid synthesis) and from which longer fatty acids can be produced.


Palmitate negatively feeds back on acetyl-CoA carboxylase (ACC) which is responsible for converting acetyl-ACP to malonyl-ACP on the growing acyl chain, thus preventing further palmitate generation
Palmitic acid (hexadecanoic acid) is a saturated fatty acid that targets proteins to cell membranes


Palmitic acid (hexadecanoic acid), a 16 carbon saturated fatty acid, has been reported to target proteins to cell membranes.
Palmitic acid (hexadecanoic acid) has been found to promote triglyceride accumulation and also affect cell viability.
Triglyceride accumulation in goose hepatocytes shows the ability to induce apoptosis.


Palmitic acid (hexadecanoic acid) is a saturated fatty acid used in hair care, cosmetics, soaps, paint, rubber, food, pharmaceuticals, animal feed and textiles.
Palmitic acid (hexadecanoic acid) is one of the most common saturated fatty acids found in animals and plants, a saturated fatty acid found in fats and waxes including olive oil, palm oil, and body lipids.


Palmitic acid (hexadecanoic acid) is one of the most common 16 carbon saturated fatty acids found in animals and plants.
Palmitic acid (hexadecanoic acid) occurs as the glyceryl ester in many oils and fats.
Palmitic acid (hexadecanoic acid) has been reported to target proteins to cell membranes.


Palmitic acid (hexadecanoic acid), also known as palmitate or C16, belongs to the class of organic compounds known as long-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.
Palmitic acid (hexadecanoic acid) is a very hydrophobic molecule, practically insoluble in water and relatively neutral.


Palmitic acid (hexadecanoic acid) is one of the most common saturated fatty acids found in animals, plants, and microorganisms.
As its name indicates, Palmitic acid (hexadecanoic acid) is a major component of the oil from the fruit of oil palms (palm oil).
In humans and other mammals, excess carbohydrates in the body are converted to palmitic acid.


Palmitic acid (hexadecanoic acid) is the first fatty acid produced during fatty acid synthesis and is the precursor to longer fatty acids.
As a consequence, Palmitic acid (hexadecanoic acid) is a major lipid component of animals.
Palmitic acid (hexadecanoic acid) has been detected, but not quantified in, several different foods, such as sea-buckthornberries, avocado, star fruits, babassu palms, and acerola.



USES and APPLICATIONS of PALMITIC ACID (HEXADECANOIC ACID):
Cosmetic Uses of Palmitic acid (hexadecanoic acid):skin conditioning - emollient and surfactant - emulsifying.
Palmitic acid (hexadecanoic acid), as the name implies, is a fatty acid present in palm oil.
Palmitic acid (hexadecanoic acid) can also be derived from many other plant and vegetable sources — in fact, it is the most commonly occurring natural fatty acid in the world.


As a result of this ubiquity, Palmitic acid (hexadecanoic acid) has a wide range of uses in manufacturing and other applications.
Palmitic acid (hexadecanoic acid) is inexpensive and easy to produce, making it an excellent choice for many industrial applications.
Palmitic acid (hexadecanoic acid) is used in the production of soaps, detergents and cosmetics as an emulsifier.


Palmitic acid (hexadecanoic acid) is also a texturing agent for foods, a waxy cover for fruits and vegetables, and a source of anionic and nonionic surfactants and esters.
Palmitic acid (hexadecanoic acid) can be further refined or combined with other chemical agents to produce isopropyl palmitate, cetyl alcohol and other additives.


Personal Care uses of Palmitic acid (hexadecanoic acid): Emulsifier for Facial Creams and Lotions, often used in Shaving Cream Formulations.
Waxes uses of Palmitic acid (hexadecanoic acid): Fruit Wax Formulations.
Surfactants and Esters uses of Palmitic acid (hexadecanoic acid): Anionic and Nonionic Surfactants.


Food and Beverage uses of Palmitic acid (hexadecanoic acid): Raw Material for Emulsifiers.
Soaps and Detergents uses of Palmitic acid (hexadecanoic acid): Intermediate.
Palmitic acid (hexadecanoic acid) is commonly used in personal care products and cosmetics.


Palmitic acid (hexadecanoic acid) is used to produce soaps, cosmetics, and industrial mould release agents.
Palmitic acid (hexadecanoic acid) can promote smooth skin, so it’s found in many soaps.
Additionally, the popular ingredient beeswax, often found in personal care items, also houses Palmitic acid (hexadecanoic acid).


Cosmetic-wise, Palmitic acid (hexadecanoic acid) can be found in makeup used to hide imperfections such as pimples and blackheads.
Another common use for Palmitic acid (hexadecanoic acid) is in cleaning products, typically surface-active agents, such as detergent.
Palmitic acid (hexadecanoic acid) is also used when making metallic palmitates, food-grade additives, and lube oils.


Palmitic acid (hexadecanoic acid) has several uses.
For example, Palmitic acid (hexadecanoic acid) can be used to test the hardness in water and is a part of the intravenous ultrasonic contrast agent Levovist, which is used during ultrasounds to detect certain diseases.


Palmitic acid (hexadecanoic acid) is used to produce soaps, cosmetics, and industrial mould release agents.
These applications use sodium palmitate, which is commonly obtained by saponification of palm oil.
To this end, palm oil triglycerides, rendered from palm trees (species Elaeis guineensis), are treated with sodium hydroxide (in the form of caustic soda or lye), which causes hydrolysis of the ester groups, yielding glycerol and sodium palmitate.


Aluminium salts of Palmitic acid (hexadecanoic acid) and naphthenic acid were combined during World War II to produce napalm.
The word "napalm" is derived from the word’s naphthenic acid and Palmitic acid (hexadecanoic acid).
Palmitic acid (hexadecanoic acid) is also used in the determination of water hardness and is a surfactant of Levovist, an intravenous ultrasonic contrast agent.


Palmitic acid (hexadecanoic acid) can be used in the production of soaps and other personal care products.
Its surfactant properties make it an effective cleanser, while Palmitic acid (hexadecanoic acid) also has emollient applications in skincare, helping soften skin and retain moisture.


This high purity fatty acid, Palmitic acid (hexadecanoic acid), is ideal as a standard and for biological studies.
Palmitic acid (hexadecanoic acid) is considered the most abundant saturated fatty acid in nature comprising 20-30% of the lipids in many animal tissues.
Palmitic acid (hexadecanoic acid) has been found to cause reduced insulin activity due to its mediation of PKC- activation in the central nervous system.


During the metabolism of Palmitic acid (hexadecanoic acid) it is converted to the omegahydroxy hexadecanoic acid and then to the dicarboxylic hexadecanedioc acid.
Long chain fatty acids have been found to inhibit the double-stranded DNA binding activity of p53 DNA binding domain suggesting that fatty acids in the cell membrane might regulate the activity of p53 for cell division, cell-cycle checkpoint, and tumor suppression.


Saturated fatty acids, such as Palmitic acid (hexadecanoic acid), induce apoptosis in beta-cells which can lead to the development of diabetes.
Long chain fatty acids acylated to sphingolipids are critical in many biological functions and substantial amounts are found to be amide-linked to the long-chain sphingoid base sphinganine, forming a ceramide, which constitutes the lipid backbone of sphingomyelin and other sphingolipids.


Long chain fatty acids can often be found in esterified linkages with cholesterol, gangliosides, galactocerebrosides, sphingomyelin, and phosphatidylcholine.
Palmitic acid (hexadecanoic acid) is a fatty used as a food additive and emollient or surfactant in cosmetics.


Palmitic acid (hexadecanoic acid), also known as palmic acid, is a fatty acid found in plants, animals, and microorganisms and is primarily used to produce cosmetics, soaps, and release agents.
Palmitic acid (hexadecanoic acid) has been used to synthesize Musk R1, 10-hydroxy-2-decylenic acid (queen acid), as the intermediates of new drug for resistance to senile dementia -idebenone, and other medicine ,etc.


Palmitic acid (hexadecanoic acid) has been used as the sebaceous secrete inhibitor in cosmetics.
Palmitic acid (hexadecanoic acid) can be also used in electric industry.
Palmitic acid (hexadecanoic acid) in IUPAC nomenclature, is the most common saturated fatty acid found in animals, plants and microorganisms.


Palmitic acid (hexadecanoic acid) is used as a thickening agent of napalm used in military actions.
Palmitic acid (hexadecanoic acid) is used to produce soaps, cosmetics, and industrial mould release agents.
These applications use sodium palmitate, which is commonly obtained by saponification of palm oil.


To this end, palm oil triglycerides, rendered from palm trees (species Elaeis guineensis), are treated with sodium hydroxide (in the form of caustic soda or lye), which causes hydrolysis of the ester groups, yielding glycerol and sodium palmitate.
Aluminium salts of palmitic acid and naphthenic acid were combined during World War II to produce napalm.


The word "napalm" is derived from the word’s naphthenic acid and palmitic acid.
Palmitic acid (hexadecanoic acid) is also used in the determination of water hardness and is a surfactant of Levovist, an intravenous ultrasonic contrast agent.


Palmitic acid (hexadecanoic acid) is a saturated fatty acid used in hair care, cosmetics, soaps, paint, rubber, food, pharmaceuticals, animal feed and textiles.
Palmitic acid (hexadecanoic acid) is used to prepare sodium palmitate which is a natural additive in organic products.


Palmitic acid (hexadecanoic acid) is involved in the preparation of cetyl alcohol utilized in the preparation of detergents and cosmetics.
Palmitic acid (hexadecanoic acid) is used to prepare sodium palmitate which is a natural additive in organic products.
Palmitic acid (hexadecanoic acid) is involved in the preparation of cetyl alcohol utilized in the preparation of detergents and cosmetics.


Palmitic acid (hexadecanoic acid) is a saturated fatty acid that is found in many animal and vegetable fats.
Palmitic acid (hexadecanoic acid) has been used as a model system for studying the effects of salt on enzyme activity, specifically in the murine sarcoma virus.


Palmitic acid (hexadecanoic acid) has also been shown to have significant cytotoxicity at low concentrations due to its ability to inhibit protein synthesis, which may be due to receptor activity or phase transition temperature.
Palmitic acid (hexadecanoic acid) has been shown to have bioactive properties that include anti-inflammatory and antioxidant effects, as well as the ability to protect against reactive oxygen species and apoptosis.



BIOLOGICAL SOURCES OF PALMITIC ACID (HEXADECANOIC ACID):
Palmitic acid (hexadecanoic acid) occurs in the form of esters (glycerides) in oils and fats of vegetable and animal origin.
Palmitic acid (hexadecanoic acid) usually obtained from palm oil.
Palmitic acid (hexadecanoic acid) is widely distributed in plants.
Palmitic acid (hexadecanoic acid) is used in determination of water hardness.



ALTERNATIVE PARENTS OF PALMITIC ACID (HEXADECANOIC ACID):
*Straight chain fatty acids
*Monocarboxylic acids and derivatives
*Carboxylic acids
*Organic oxides
*Hydrocarbon derivatives
*Carbonyl compounds



SUBSTITUENTS OF PALMITIC ACID (HEXADECANOIC ACID):
*Long-chain fatty acid
*Straight chain fatty acid
*Monocarboxylic acid or derivatives
*Carboxylic acid
*Carboxylic acid derivative
*Organic oxygen compound
*Organic oxide
*Hydrocarbon derivative
*Organooxygen compound
*Carbonyl group
*Aliphatic acyclic compound



SOLUBILITY OF PALMITIC ACID (HEXADECANOIC ACID):
Palmitic acid (hexadecanoic acid) is soluble in hot alcohol, acetone, benzene, ethyl ether, amyl acetate, propyl alcohol and chloroform. Palmitic acid (hexadecanoic acid) is slightly soluble in cold alcohol and petroleum ether. Insoluble in water.



BIOCHEMISTRY OF PALMITIC ACID (HEXADECANOIC ACID):
Palmitic acid (hexadecanoic acid) is the first fatty acid produced during fatty acid synthesis and is the precursor to longer fatty acids.
As a consequence, Palmitic acid (hexadecanoic acid) is a major body component of animals.
In humans, one analysis found Palmitic acid (hexadecanoic acid) to make up 21–30% (molar) of human depot fat, and it is a major, but highly variable, lipid component of human breast milk.

Palmitate negatively feeds back on acetyl-CoA carboxylase (ACC), which is responsible for converting acetyl-CoA to malonyl-CoA, which in turn is used to add to the growing acyl chain, thus preventing further palmitate generation.
Some proteins are modified by the addition of a palmitoyl group in a process known as palmitoylation.
Palmitoylation is important for localisation of many membrane proteins.



OCCURRENCE AND PRODUCTION OF PALMITIC ACID (HEXADECANOIC ACID):
Palmitic acid (hexadecanoic acid) was discovered by Edmond Frémy in 1840, in saponified palm oil.
This remains the primary industrial route for its production, with the triglycerides (fats) in palm oil being hydrolysed by high-temperature water, and the resulting mixture fractionally distilled.



DIETARY SOURCES OF PALMITIC ACID (HEXADECANOIC ACID):
Palmitic acid (hexadecanoic acid) is produced by a wide range of other plants and organisms, typically at low levels.
Palmitic acid (hexadecanoic acid) is present in butter, cheese, milk, and meat, as well as cocoa butter, olive oil, soybean oil, and sunflower oil.
Karukas contain 44.90% Palmitic acid (hexadecanoic acid).
The cetyl ester of Palmitic acid (hexadecanoic acid), cetyl palmitate, occurs in spermaceti.



MILITARY OF PALMITIC ACID (HEXADECANOIC ACID):
Aluminium salts of Palmitic acid (hexadecanoic acid) and naphthenic acid were the gelling agents used with volatile petrochemicals during World War II to produce napalm.
The word "napalm" is derived from the words naphthenic acid and Palmitic acid (hexadecanoic acid).



RESEARCH OF PALMITIC ACID (HEXADECANOIC ACID):
It is well accepted in the medical community that Palmitic acid (hexadecanoic acid) from dietary sources raises low-density lipoprotein (LDL) and total cholesterol.
The World Health Organization have stated there is convincing evidence that Palmitic acid (hexadecanoic acid) increases cardiovascular disease risk.
A 2021 review indicated that replacing dietary Palmitic acid (hexadecanoic acid) and other saturated fatty acids with unsaturated fatty acids, such as oleic acid, could reduce several biomarkers of cardiovascular and metabolic diseases.



PHYSICAL and CHEMICAL PROPERTIES of PALMITIC ACID (HEXADECANOIC ACID):
Chemical formula: C16H32O2
Molar mass: 256.430 g/mol
Appearance: White crystals
Density: 0.852 g/cm3 (25 °C)
0.8527 g/cm3 (62 °C)
Melting point: 62.9 °C (145.2 °F; 336.0 K)
Boiling point: 351–352 °C (664–666 °F; 624–625 K)
271.5 °C (520.7 °F; 544.6 K), 100 mmHg
215 °C (419 °F; 488 K), 15 mmHg
Solubility in water: 4.6 mg/L (0 °C)
7.2 mg/L (20 °C)
8.3 mg/L (30 °C)
10 mg/L (45 °C)
12 mg/L (60 °C)

Solubility: Soluble in amyl acetate, alcohol, CCl4,C6H6
Very soluble in CHCl3
Solubility in ethanol 2 g/100 mL (0 °C)
2.8 g/100 mL (10 °C)
9.2 g/100 mL (20 °C)
31.9 g/100 mL (40 °C)
Solubility in methyl acetate: 7.81 g/100 g
Solubility in ethyl acetate: 10.7 g/100 g
Vapor pressure: 0.051 mPa (25 °C)
1.08 kPa (200 °C)
28.06 kPa (300 °C)
Acidity (pKa): 4.75
Magnetic susceptibility (χ): −198.6·10−6 cm3/mol
Refractive index (nD): 1.43 (70 °C)

Viscosity: 7.8 cP (70 °C)
Thermochemistry
Heat capacity (C): 463.36 J/(mol·K)
Std molar entropy (S⦵298): 452.37 J/(mol·K)
Std enthalpy of formation (ΔfH⦵298): −892 kJ/mol
Std enthalpy of combustion (ΔcH⦵298): 10030.6 kJ/mol
Molecular Weight: 256.42 g/mol
XLogP3: 6.4
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 14
Exact Mass: 256.240230259 g/mol
Monoisotopic Mass: 256.240230259 g/mol
Topological Polar Surface Area: 37.3Ų

Heavy Atom Count: 18
Formal Charge: 0
Complexity:178
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Physical state: solid
Color: white
Odor: No data available
Melting point/freezing point:
Melting point/range: 60 - 65 °C

Initial boiling point and boiling range: 271,5 °C at 133 hPa
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: 113 °C
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: 7,8 mPa.s at 70 °C
Water solubility: 0,00005 g/l at 20 °C
Partition coefficient:
n-octanol/water: log Pow: 7,17

Vapor pressure: 13 hPa at 210 °C
Density: 0,852 g/cm3 at 62 °C
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: none
Other safety information:
Bulk density: 415 kg/m3
Surface tension: 28,2 mN/m at 70 °C
Chemical Formula: C16H32O2
Average Molecular Weight: 256.4241
Monoisotopic Molecular Weight: 256.240230268
IUPAC Name: hexadecanoic acid

Traditional Name: palmitic acid
CAS Registry Number: 57-10-3
SMILES: CCCCCCCCCCCCCCCC(O)=O
InChI Identifier: InChI=1S/C16H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-15H2,1H3,(H,17,18)
InChI Key: IPCSVZSSVZVIGE-UHFFFAOYSA-N
Melting Point: 61.8 °C Not Available
Boiling Point: Not Available Not Available
Water Solubility: 4.0e-05 mg/mL Not Available
LogP: 7.17
Melting Point: 61-62.5 °C(lit.)
Boiling Point: 340.6±5.0 °C at 760 mmHg
Flash Point: 154.1±12.5 °C
Molecular Formula: C16H32O2
Molecular Weight: 256.424

Density: 0.9±0.1 g/cm3
Appearance: white to pale yellow crystalline solid (est)
Assay: 96.00 to 100.00
Water Content: <0.20%
Food Chemicals Codex Listed: Yes
Melting Point: 61.00 to 64.00 °C. @ 760.00 mm Hg
Boiling Point: 204.00 to 220.00 °C. @ 760.00 mm Hg
Congealing Point: 53.30 to 62.00 °C.
Saponification Value: 205.00 to 221.00
Unsaponifiable Matter: <1.50%
Vapor Pressure: 10.000000 mmHg @ 210.00 °C.
Flash Point: 238.00 °F. TCC ( 114.44 °C. )
logP (o/w): 7.170

Soluble in:alcohol, chloroform, ether
water, 0.04 mg/L @ 25 °C (exp)
Insoluble in: water
CAS number: 57-10-3
EC number: 200-312-9
Hill Formula: C₁₆H₃₂O₂
Chemical formula: CH₃(CH₂)₁₄COOH
Molar Mass: 256.43 g/mol
HS Code: 2915 70 11
Boiling point: 271.4 °C (133 hPa)
Density: 0.852 g/cm3
Flash point: 113 °C
Melting Point: 60 - 65 °C
Vapor pressure: 13 hPa (210 °C)

Bulk density: 415 kg/m3
Water Solubility: 0.00041 g/L
logP: 7.23
logP: 6.26
logS: -5.8
pKa (Strongest Acidic): 4.95
Physiological Charge: -1
Hydrogen Acceptor Count: 2
Hydrogen Donor Count: 1
Polar Surface Area: 37.3 Ų
Rotatable Bond Count: 14
Refractivity: 77.08 m³·mol⁻¹
Polarizability: 34.36 ų
Number of Rings: 0

Bioavailability: No
Rule of Five: No
Ghose Filter: No
Veber's Rule: No
MDDR-like Rule: No
Chemical Formula: C16H32O2
IUPAC name: hexadecanoic acid
InChI Identifier: InChI=1S/C16H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-15H2,1H3,(H,17,18)
InChI Key: IPCSVZSSVZVIGE-UHFFFAOYSA-N
Isomeric SMILES: CCCCCCCCCCCCCCCC(O)=O
Average Molecular Weight: 256.4241
Monoisotopic Molecular Weight: 256.240230268
CAS number: 57-10-3
Weight Average: 256.4241

Monoisotopic: 256.240230268
InChI Key: IPCSVZSSVZVIGE-UHFFFAOYSA-N
InChI: InChI=1S/C16H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-15H2,1H3,(H,17,18)
IUPAC Name: hexadecanoic acid
Traditional IUPAC Name: palmitic acid
Chemical Formula: C16H32O2
SMILES: [H]OC(=O)C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H]
ΔcH°liquid: [-10028.60; -9977.20] kJ/mol
ΔcH°solid: -9977.60 ± 8.80 kJ/mol
ΔfG°: -181.90 kJ/mol
ΔfH°gas: -730.00 ± 5.50 kJ/mol
ΔfH°liquid: -848.40 ± 2.20 kJ/mol
ΔfusH°: [52.55; 53.50] kJ/mol
ΔsubH°: 194.00 ± 11.00 kJ/mol
ΔvapH°: 74.64 kJ/mol
log10WS: -6.81
logPoct/wat: 5.552
McVol: 243.740 ml/mol

Pc: 1468.41 ± 85.00 kPa
Ptriple: 8.27e-06 ± 4.00e-06 kPa
Inp: [321.57; 2010.00]
I: [2871.00; 2954.00]
S°solid,1 bar: [438.65; 543.50] J/mol×K
Tboil: 612.15 ± 6.00 K
Tc: 785.22 ± 3.00 K
Tfus: [334.85; 337.22] K
Ttriple: [335.05; 336.25] K
Cp,gas: [719.80; 805.28] J/mol×K [711.53; 880.17]
Cp,solid: [448.00; 678.00] J/mol×K [292.50; 373.00]
η: [0.0000353; 0.0035737] Pa×s [380.83; 711.53]
ΔfusH: [47.00; 54.94] kJ/mol [332.70; 336.50]
ΔsubH: [134.00; 154.40] kJ/mol [288.00; 326.50]
ΔvapH: [90.10; 121.60] kJ/mol [298.00; 532.50]
Pvap: [1.33; 9.33] kPa [483.30; 533.40]
ΔfusS: [163.50; 163.50] J/mol×K [335.73; 336.00]



FIRST AID MEASURES of PALMITIC ACID (HEXADECANOIC ACID):
-Description of first-aid measures:
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Remove contact lenses.
*If swallowed:
After swallowing:
Make victim drink water (two glasses at most).
Consult doctor if feeling unwell.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of PALMITIC ACID (HEXADECANOIC ACID):
-Environmental precautions:
No special precautionary measures necessary.
-Methods and materials for containment and cleaning up:
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of PALMITIC ACID (HEXADECANOIC ACID):
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
none



EXPOSURE CONTROLS/PERSONAL PROTECTION of PALMITIC ACID (HEXADECANOIC ACID):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection
Safety glasses
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Respiratory protection:
Recommended Filter type: Filter type P1
-Control of environmental exposure:
No special precautionary measures necessary



HANDLING and STORAGE of PALMITIC ACID (HEXADECANOIC ACID):
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
Recommended storage temperature see product label.



STABILITY and REACTIVITY of PALMITIC ACID (HEXADECANOIC ACID):
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Conditions to avoid:
Strong heating.
-Incompatible materials:
No data available



SYNONYMS:
Palmitic Acid, Hexadecanoic Acid
Hexadecanoic acid
Palmitic acid
C16:0 (Lipid numbers)
palmitic acid
Hexadecanoic acid
57-10-3
Cetylic acid
palmitate
n-Hexadecanoic acid
Hexadecylic acid
Hydrofol
n-Hexadecoic acid
1-Pentadecanecarboxylic acid
Palmitinic acid
hexaectylic acid
Pentadecanecarboxylic acid
hexadecoic acid
1-Hexyldecanoic Acid
Industrene 4516
Emersol 140
Emersol 143
Hystrene 8016
Hystrene 9016
Palmitinsaeure
Palmitic acid, pure
Palmitic acid 95%
Kortacid 1698
FEMA No. 2832
Loxiol EP 278
Palmitic acid (natural)
Hydrofol Acid 1690
Cetyl acid
Prifac 2960
C16:0
HSDB 5001
Pristerene 4934
Pristerene-4934
Edenor C16
NSC 5030
AI3-01594
Lunac P 95KC
Lunac P 95
Lunac P 98
CCRIS 5443
Prifac-2960
CHEBI:15756
NSC5030
NSC-5030
EINECS 200-312-9
UNII-2V16EO95H1
FA 16:0
BRN 0607489
Palmitic acid (NF)
DTXSID2021602
Glycon P-45
IMEX C 1498
2V16EO95H1
Hexadecanoic acid (9CI)
MFCD00002747
Palmitic acid (7CI,8CI)
CHEMBL82293
DTXCID101602
CH3-[CH2]14-COOH
EC 200-312-9
4-02-00-01157 (Beilstein Handbook Reference)
n-hexadecoate
LMFA01010001
PA 900
EDENOR C 16-98-100
67701-02-4
FA 1695
SURFAXIN COMPONENT PALMITIC ACID
1-hexyldecanoate
NCGC00164358-01
LUCINACTANT COMPONENT PALMITIC ACID
pentadecanecarboxylate
Hexadecanoic acid 10 microg/mL in Acetonitrile
HEXADECANOIC-11,11,12,12-D4 ACID
PALMITIC ACID (II)
PALMITIC ACID [II]
PALMITIC ACID (MART.)
PALMITIC ACID [MART.]
CH3-(CH2)14-COOH
Palmitic acid
Hexadecanoic acid
PLM
palmic acid
Hexadecanoate (n-C16:0)
PALMITIC ACID (EP MONOGRAPH)
PALMITIC ACID [EP MONOGRAPH]
Acid, Palmitic
CAS-57-10-3
Acid, Hexadecanoic
SR-01000944716
Palmitic acid [USAN:NF]
palmitoate
Hexadecoate
Palmitinate
Palmitinsaure
palmitic-acid
palmitoic acid
Hexadecanoicacid
Aethalic acid
Hexadecanoic acid Palmitic acid
2hmb
2hnx
Palmitic acid_jeyam
n-Hexadecyclic Acid
fatty acid 16:0
Palmitic Acid, FCC
Kortacid 1695
Palmitic acid_RaGuSa
Univol U332
1219802-61-5
Prifrac 2960
Hexadecanoic acid anion
Hexadecanoic--d5 Acid
3v2q
Palmitic acid, >=99%
bmse000590
Epitope ID:141181
CETYL ACID [VANDF]
PALMITIC ACID [MI]
SCHEMBL6177
PALMITIC ACID [DSC]
PALMITIC ACID [FCC]
PALMITIC ACID [FHFI]
PALMITIC ACID [HSDB]
PALMITIC ACID [INCI]
PALMITIC ACID [USAN]
FAT
WLN: QV15
P5585_SIGMA
PALMITIC ACID [VANDF]
GTPL1055
QSPL 166
PALMITIC ACID [USP-RS]
PALMITIC ACID [WHO-DD]
(1(1)(3)C)hexadecanoic acid
1b56
HMS3649N08
Palmitic acid, analytical standard
Palmitic acid, BioXtra, >=99%
Palmitic acid, Grade II, ~95%
HY-N0830
Palmitic acid, natural, 98%, FG
Tox21_112105
Tox21_201671
Tox21_302966
AC9381
BDBM50152850
s3794
Palmitic acid, >=95%, FCC, FG
AKOS005720983
Tox21_112105_1
CCG-267027
CR-0047
DB03796
Palmitic acid, for synthesis, 98.0%
NCGC00164358-02
NCGC00164358-03
NCGC00256424-01
NCGC00259220-01
BP-27917
Palmitic acid, purum, >=98.0% (GC)
SY006518
CS-0009861
FT-0626965
FT-0772579
P0002
P1145
Palmitic acid, SAJ first grade, >=95.0%
EN300-19603
C00249
D05341
Palmitic acid, Vetec(TM) reagent grade, 98%
PALMITIC ACID (CONSTITUENT OF SPIRULINA)
Palmitic acid, >=98% palmitic acid basis (GC)
A831313
Q209727
PALMITIC ACID (CONSTITUENT OF FLAX SEED OIL)
PALMITIC ACID (CONSTITUENT OF SAW PALMETTO)
SR-01000944716-1
SR-01000944716-2
BA71C79B-C9B1-451A-A5BE-B480B5CC7D0C
PALMITIC ACID (CONSTITUENT OF BORAGE SEED OIL)
PALMITIC ACID (CONSTITUENT OF SPIRULINA) [DSC]
F0001-1488
Z104474418
PALMITIC ACID (CONSTITUENT OF EVENING PRIMROSE OIL)
PALMITIC ACID (CONSTITUENT OF SAW PALMETTO) [DSC]
Palmitic acid, certified reference material, TraceCERT(R)
Palmitic acid, European Pharmacopoeia (EP) Reference Standard
Palmitic acid, United States Pharmacopeia (USP) Reference Standard
Palmitic acid, Pharmaceutical Secondary Standard; Certified Reference Material
Sodium Palmitate
Palmitic acid sodium salt
Sodium hexadecanoate
Sodium pentadecanecarboxylate
HSDB 759
n-Hexadecanoic acid
Palmitic acid
1-Pentadecanecarboxylic acid
Cetostearic acid
Pentadecanecarboxylic acid
Palmitinic acid
(E)-[p-((1,2-Dihydroxypropyloxy)-p′-(propargyloxy)] azobenzene
Palmitates, Cetylic acid
NSC 5030
n-Hexadecoic acid
Hexadecanoic acid
n-Hexadecoic acid
Palmitic acid
Pentadecanecarboxylic acid
1-Pentadecanecarboxylic acid
Cetylic acid
Emersol 140
Emersol 143
Hexadecylic acid
Hydrofol
Hystrene 8016
Hystrene 9016
Industrene 4516
Glycon P-45
Prifac 2960
NSC 5030
Palmitinic acid
Kortacid 1695
60605-23-4
116860-99-2
212625-86-0
Hexadecanoic acid (palmitic acid)
Hexadecanoic (palmitic) acid
Palmitic acid (hexadecanoic acid)
1-Hexyldecanoic acid
1-Pentadecanecarboxylic acid
16:00
C16
C16 Fatty acid
C16:0
Cetylic acid
CH3-[CH2]14-COOH
FA 16:0
Hexadecanoate
Hexadecoic acid
Hexadecylic acid
Hexaectylic acid
N-Hexadecanoic acid
N-Hexadecoic acid
Palmitate
Palmitinic acid
Palmitinsaeure
Pentadecanecarboxylic acid
1-Hexyldecanoate
1-Pentadecanecarboxylate
Cetylate
Hexadecanoic acid
Hexadecoate
Hexadecylate
Hexaectylate
N-Hexadecanoate
N-Hexadecoate
Palmitinate
Pentadecanecarboxylate
Edenor C16
Emersol 140
Emersol 143
Glycon p-45
Hexadecanoate (N-C16:0)
Hexadecanoic acid palmitic acid
Hydrofol
Hydrofol acid 1690
Hystrene 8016
Hystrene 9016
Industrene 4516
Kortacid 1698
Loxiol ep 278
Lunac p 95
Lunac p 95KC
Lunac p 98
Palmitoate
Palmitoic acid
PAM
PLM
Prifac 2960
Prifrac 2960
Pristerene 4934
Univol u332
Acid, hexadecanoic
Acid, palmitic
FA(16:0)
n-hexadecanoic acid
1-hexadecanoic acid
hexdecanoic acid
Hexadecanoic acid
MFCD00002747
EINECS 200-312-9
Neo-Fat 16
Palmitic acid
1-Hexyldecanoate
1-Hexyldecanoic acid
1-Pentadecanecarboxylate
1-Pentadecanecarboxylic acid
16:00
Acid, hexadecanoic
Acid, palmitic
Aethalic acid
C16
C16 Fatty acid
C16 fatty acid
C16:0
Cetylate
Cetylic acid
CH3-[CH2]14-COOH
Edenor C16
Emersol 140
Emersol 143
FA 16:0
FA(16:0)
FEMA 2832
Glycon p-45
Glycon P-45
Hexadecanoate
Hexadecanoate (N-C16:0)
Hexadecanoic acid
Hexadecanoic acid (9CI)
Hexadecanoic acid palmitic acid
Hexadecoate
Hexadecoic acid
Hexadecylate
Hexadecylic acid
Hexaectylate
Hexaectylic acid
Hydrofol
Hydrofol acid 1690
Hystrene 8016
Hystrene 9016
Industrene 4516
Kortacid 1698
Loxiol ep 278
Lunac p 95
Lunac P 95
Lunac p 95KC
Lunac P 95kc
Lunac p 98
Lunac P 98
N-Hexadecanoate
N-Hexadecanoic acid
N-Hexadecoate
N-Hexadecoic acid
Palmitate
Palmitic acid
Palmitic acid, USAN
Palmitinate
Palmitinic acid
Palmitinsaeure
Palmitoate
Palmitoic acid
PAM
1-hexyldecanoate
1-hexyldecanoic acid
1-Pentadecanecarboxylic acid
C16 fatty acid
Cetylic acid
Coconut oil fatty acids
Edenor C16
Hexadecanoate
Hexadecanoic (palmitic) acid
Hexadecanoic acid
Hexadecanoic acid (palmitic acid)
Hexadecanoic acid palmitic acid
Hexadecoate
Hexadecoic acid
Hexadecylic acid
Hexaectylic acid
Hydrofol
n-Hexadecanoate
n-Hexadecanoic acid
n-Hexadecoate
n-Hexadecoic acid
Palmitate
palmitic acid
Palmitinate
Palmitinic acid
Palmitinsaeure
palmitoate
palmitoic acid
PAM
Pentadecanecarboxylate
Pentadecanecarboxylic acid
PLM
16:00
C16
C16:0
CH3-[CH2]14-COOH
FA 16:0
1-Pentadecanecarboxylate
Cetylate
Hexadecylate
Hexaectylate
Emersol 140
Emersol 143
Glycon p-45
Hexadecanoate (N-C16:0)
Hydrofol acid 1690
Hystrene 8016
Hystrene 9016
Industrene 4516
Kortacid 1698
Loxiol ep 278
Lunac p 95
Lunac p 95KC
Lunac p 98
Prifac 2960
Prifrac 2960
Pristerene 4934
Univol u332
Acid, hexadecanoic
Acid, palmitic
FA(16:0)
C16H32O2
Hexadecanoic Acid
Cetylic Acid
Palmitate
n-Hexadecanoic Acid
Hexadecanoic Acid Palmitic Acid
1 Pentadecanecarboxylic Acid
Pentadecanecarboxylic Acid
1 Pentadecanecarboxylate
Hexadecanoate (N C16:0)
Pentadecanecarboxylate
1 Hexyldecanoic Acid
N Hexadecanoic Acid
Hydrofol Acid 1690
Acid, Hexadecanoic
16:00
N Hexadecoic Acid
Hexadecanoic Acid
Ch3 [Ch2]14 Cooh
Hexadecylic Acid
Hexaectylic Acid
1 Hexyldecanoate
Hexadecoic Acid
Palmitinic Acid
N Hexadecanoate
Industrene 4516
Pristerene 4934
C16 Fatty Acid
Palmitinsaeure
Palmitoic Acid
Acid, Palmitic
Hexadecanoate
N Hexadecoate
Hystrene 8016
Hystrene 9016
Kortacid 1698
Loxiol Ep 278
Cetylic Acid
Hexadecylate
Hexaectylate
Lunac P 95 Kc
Prifrac 2960
Hexadecoate
Palmitinate
Emersol 140
Emersol 143
Glycon P 45
Prifac 2960
Univol U332
Edenor C16
Lunac P 95
Lunac P 98
Palmitoate
Palmitate
Cetylate
Hydrofol
Fa(16:0)
C16:0
C16
Pam
Plm



PALMITIK ASIT 
PALMITOYL TRIPEPTIDE-1, N° CAS : 147732-56-7. Nom INCI : PALMITOYL TRIPEPTIDE-1. Nom chimique : L-Lysine, N-(1-oxohexadecyl)glycyl-L-histidyl-. N° EINECS/ELINCS : Ses fonctions (INCI): Agent d'entretien de la peau : Maintient la peau en bon état
P-ANISIC ACID
P-ANISIC ACID p-Anisic acid p-Anisic acid[1] Skeletal formula of p-anisic acid Ball-and-stick model of the p-anisic acid molecule Names IUPAC name 4-Methoxybenzoic acid Other names Draconic acid Identifiers CAS Number 100-09-4 3D model (JSmol) Interactive image ChEBI CHEBI:40813 ChEMBL ChEMBL21932 ChEMBL1762657 ChemSpider 10181338 ECHA InfoCard 100.002.562 PubChem CID 7478 Properties Chemical formula C8H8O3 Molar mass 152.149 g·mol−1 Density 1.385 g/cm3 Melting point 184 °C (363 °F; 457 K) (sublimation) Boiling point 275 to 280 °C (527 to 536 °F; 548 to 553 K) Solubility in water 1 part per 2500 Structure[2] Crystal structure monoclinic Space group P21/a Lattice constant a = 16.98 Å, b = 10.95 Å, c = 3.98 Å α = 90°, β = 98.7°, γ = 90° Formula units (Z) 4 Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references p-Anisic acid, also known as 4-methoxybenzoic acid or draconic acid, is one of the isomers of anisic acid. The term "anisic acid" often refers to this form specifically. It is a white crystalline solid which is insoluble in water, highly soluble in alcohols and soluble in ether, and ethyl acetate. Synthesis and occurrence p-Anisic acid is found naturally in anise. It is generally obtained by the oxidation of anethole or p-methoxyacetophenone. Uses p-Anisic acid has antiseptic properties. It is also used as an intermediate in the preparation of more complex organic compounds. Properties mp 182-185 °C (lit.) SMILES string COc1ccc(cc1)C(O)=O InChI 1S/C8H8O3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3,(H,9,10) InChI key ZEYHEAKUIGZSGI-UHFFFAOYSA-N Description Biochem/physiol Actions Metabolite of aniracetam that mimics its anxiolytic actions. It is also an inhibitor of tyrosinase. p-Anisic Acid What: p-Anisic acid is found naturally in anise. p-Anisic Acid is a white crystalline solid which is insoluble in water and soluble in alcohols, ether, and ethyl acetate. p-Anisic acid has antiseptic properties and is used as a preservative in cosmetic products. Origin: p-Anisic acid is generally obtained by the oxidation of anethole, an aromatic compound that occurs in essential oils . Products Found In: Skincare, body care, hair care, sun protection products, anti-aging skincare. Alternative Names: P-Anisic Acid, 4-Anisic Acid, Benzoic Acid, 4-Methoxy-, Draconic Acid, 4-Methoxybenzoic Acid, P-Methoxybenzoic Acid, 4-Methoxy- Benzoic Acid, Benzoic Acid, 4methoxy, Benzoic Acid, 4-Methoxy- (9ci). Toxicity: p-Anisic Acid is generally classified as having a low toxicity rating (EWG). Molecular Weight of p-Anisic Acid: 152.15 g/mol Computed by PubChem 2.1 (PubChem release 2019.06.18) XLogP3 of p-Anisic Acid: 2 Computed by XLogP3 3.0 (PubChem release 2019.06.18) Hydrogen Bond Donor Count of p-Anisic Acid: 1 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Hydrogen Bond Acceptor Count of p-Anisic Acid: 3 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Rotatable Bond Count of p-Anisic Acid: 2 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Exact Mass of p-Anisic Acid: 152.047344 g/mol Computed by PubChem 2.1 (PubChem release 2019.06.18) Monoisotopic Mass of p-Anisic Acid: 152.047344 g/mol Computed by PubChem 2.1 (PubChem release 2019.06.18) Topological Polar Surface Area of p-Anisic Acid: 46.5 Ų Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Heavy Atom Count of p-Anisic Acid: 11 Computed by PubChem Formal Charge of p-Anisic Acid: 0 Computed by PubChem Complexity of p-Anisic Acid: 136 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Isotope Atom Count of p-Anisic Acid: 0 Computed by PubChem Defined Atom Stereocenter Count of p-Anisic Acid: 0 Computed by PubChem Undefined Atom Stereocenter Count of p-Anisic Acid: 0 Computed by PubChem Defined Bond Stereocenter Count of p-Anisic Acid: 0 Computed by PubChem Undefined Bond Stereocenter Count of p-Anisic Acid: 0 Computed by PubChem Covalently-Bonded Unit Count of p-Anisic Acid: 1 Computed by PubChem Compound of p-Anisic Acid Is Canonicalized Yes Substance identity Help EC / List no.: 202-818-5 CAS no.: 100-09-4 Mol. formula: C8H8O3 formula Hazard classification & labelling Help According to the notifications provided by companies to ECHA in REACH registrations no hazards have been classified. About p-Anisic Acid Helpful information p-Anisic Acid has not been registered under the REACH Regulation, therefore as yet ECHA has not received any data about p-Anisic Acid from registration dossiers. p-Anisic Acid is used by consumers, by professional workers (widespread uses), in formulation or re-packing and at industrial sites. Consumer Uses p-Anisic Acid is used in the following products: cosmetics and personal care products, biocides (e.g. disinfectants, pest control products), perfumes and fragrances, pharmaceuticals and washing & cleaning products. Other release to the environment of p-Anisic Acid is likely to occur from: indoor use as processing aid and outdoor use as processing aid. Article service life ECHA has no public registered data on the routes by which p-Anisic Acid is most likely to be released to the environment. ECHA has no public registered data indicating whether or into which articles the substance might have been processed. Widespread uses by professional workers p-Anisic Acid is used in the following products: cosmetics and personal care products, perfumes and fragrances, pharmaceuticals and washing & cleaning products. p-Anisic Acid is used in the following areas: health services. Other release to the environment of p-Anisic Acid is likely to occur from: indoor use as processing aid and outdoor use as processing aid. Formulation or re-packing p-Anisic Acid is used in the following products: cosmetics and personal care products, washing & cleaning products, biocides (e.g. disinfectants, pest control products), perfumes and fragrances, pharmaceuticals and laboratory chemicals. Release to the environment of p-Anisic Acid can occur from industrial use: formulation of mixtures. Uses at industrial sites p-Anisic Acid is used in the following products: cosmetics and personal care products, biocides (e.g. disinfectants, pest control products), perfumes and fragrances, pharmaceuticals, washing & cleaning products and laboratory chemicals. p-Anisic Acid is used in the following areas: health services and scientific research and development. p-Anisic Acid is used for the manufacture of: chemicals. Release to the environment of p-Anisic Acid can occur from industrial use: in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates) and as processing aid. Manufacture ECHA has no public registered data on the routes by which p-Anisic Acid is most likely to be released to the environment. Details Though the official function of P-Anisic Acid is masking (meaning that it helps to mask not so nice smells in the product), according to manufacturer info it is rather used as a preservative. It is a skin friendly organic acid that works against fungi. SODIUM ANISATE is derived from fennel, this is the sodium salt of p-anisic acid. p-Anisic Acid is classified as antimicrobial and flavouring. p-Anisic Acid acts as an anti-fungal agent, and when paired with sodium levulinate the two ingredients make for a comprehensive preservative for cosmetics. P-Anisic Acid is approved for use in organic cosmetics. Sodium anisate (dermosoft® anisate) is an easy to use water soluble salt of an organic acid with an excellent fungicidal activity. p-Anisic Acid can be added to the cold or hot water phase at any step of the process. The combination with antimicrobial surface active substances or organic acids is recommended to improve the performance of the product even at higher pH. p-Anisic Acid p-Anisic Acid is classified as : Masking CAS Number of p-Anisic Acid 100-09-4 EINECS/ELINCS No of p-Anisic Acid: 202-818-5 COSING REF No of p-Anisic Acid: 35837 Chem/IUPAC Name of p-Anisic Acid: Benzoic acid, 4-methoxy- Description p-Anisic Acid belongs to the class of organic compounds known as p-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 4 of the benzene ring is replaced by a methoxy group.
PANTHENOL
PANTHENOL Panthenol Panthenol Stereo, skeletal formula of panthenol (R) Names IUPAC name 2,4-Dihydroxy-N-(3-hydroxypropyl)-3,3-dimethylbutanamide[1] Other names Pantothenol Pantothenyl alcohol N-Pantoylpropanolamine Bepanthen (trade name) Dexpanthenol (D form) Identifiers CAS Number 16485-10-2 ☒ 81-13-0 R ☒ 3D model (JSmol) Interactive image 3DMet B00882 Beilstein Reference 1724945, 1724947 R ChEBI CHEBI:27373 ☒ ChEMBL ChEMBL1200979 ☒ ChemSpider 4516 check 115991 R ☒ 4677984 S ☒ ECHA InfoCard 100.036.839 EC Number 240-540-6 KEGG D03726 check MeSH dexpanthenol PubChem CID 4678 131204 R 5748487 S RTECS number ES4316500 UNII 1O6C93RI7Z check CompTox Dashboard (EPA) DTXSID3044598 InChI[show] SMILES[show] Properties Chemical formula C9H19NO4 Molar mass 205.254 g·mol−1 Appearance Highly viscous, colourless liquid Density 1.2 g mL−1 (at 20 °C) Melting point 66 to 69 °C (151 to 156 °F; 339 to 342 K) [contradictory] Boiling point 118 to 120 °C (244 to 248 °F; 391 to 393 K) at 2.7 Pa log P −0.989 Acidity (pKa) 13.033 Basicity (pKb) 0.964 Chiral rotation ([α]D) +29° to +30° Refractive index (nD) 1.499 Pharmacology ATC code A11HA30 (WHO) D03AX03 (WHO), S01XA12 (WHO) Hazards NFPA 704 (fire diamond) NFPA 704 four-colored diamond 110 Lethal dose or concentration (LD, LC): LD50 (median dose) 10,100 mg kg−1 (intraperitoneal, mouse); 15,000 mg kg−1 (oral, mouse) Related compounds Related compounds Arginine Theanine Pantothenic acid Hopantenic acid Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ☒ verify (what is check☒ ?) Infobox references Panthenol (also called pantothenol) is the alcohol analog of pantothenic acid (vitamin B5), and is thus a provitamin of B5. In organisms it is quickly oxidized to pantothenic acid. It is a viscous transparent liquid at room temperature. Panthenol is used as a moisturizer and to improve wound healing in pharmaceutical and cosmetic products. Uses Bepanthen eye and nose ointment (Germany) In pharmaceuticals, cosmetics and personal-care products, panthenol is a moisturizer and humectant, used in ointments, lotions, shampoos, nasal sprays, eye drops, lozenges, and cleaning solutions for contact lenses. In ointments it is used for the treatment of sunburns, mild burns, minor skin injuries and disorders (in concentrations of up to 2–5%).[2] It improves hydration, reduces itching and inflammation of the skin, improves skin elasticity, and accelerates epidermal wounds' rate of healing.[3] For this purpose, it is sometimes combined with allantoin. It binds to the hair shaft readily; so, it is a common component of commercial shampoos and hair conditioners (in concentrations of 0.1–1%). It coats the hair and seals its surface,[citation needed] lubricating the hair shaft and giving it a shiny appearance. It is also recommended by tattoo artists as a post-tattooing moisturising cream. Adverse effects Panthenol is generally well tolerated. In rare cases, skin irritation and contact allergies have been reported.[2][3] Pharmacology Panthenol readily penetrates into the skin and mucous membranes (including the intestinal mucosa), where it is quickly oxidized to pantothenic acid. Pantothenic acid is extremely hygroscopic,[4] that is, it binds water effectively. It is also used in the biosynthesis of coenzyme A, which plays a role in a wide range of enzymatic reactions and thus in cell growth.[2][3] Physical and chemical properties Dexpanthenol Panthenol is an odourless, slightly bitter, highly viscous, transparent and colourless liquid at room temperature,[5] but salts of pantothenic acid (for example sodium pantothenate) are powders (typically white). It is easily soluble in water and alcohol, moderately soluble in diethyl ether, soluble in chloroform (1:100),[5] in propylene glycol, and slightly soluble in glycerin. Panthenol's expanded chemical formula is HO–CH2–C(CH3)2–CH(OH)–CONH–CH2CH2CH2–OH. Stereochemistry Panthenol comes in two enantiomers, D and L. Only D-panthenol (dexpanthenol) is biologically active, however both forms have moisturizing properties. For cosmetic use, panthenol comes either in D form, or as a racemic mixture of D and L (DL-panthenol). D-Panthenol D-Panthenol (also called pantothenol) is the alcohol analog of pantothenic acid (vitamin B5), and is thus a provitamin of B5. In organisms it is quickly oxidized to pantothenic acid. D-Pantenol is a viscous transparent liquid at room temperature. D-Panthenol is used as a moisturizer and to improve wound healing in pharmaceutical and cosmetic products. Bepanthen eye and nose ointment (Germany) In pharmaceuticals, cosmetics and personal-care products, D-Panthenol is a moisturizer and humectant, used in ointments, lotions, shampoos, nasal sprays, eye drops, lozenges, and cleaning solutions for contact lenses. In ointments it is used for the treatment of sunburns, mild burns, minor skin injuries and disorders (in concentrations of up to 2–5%).[2] It improves hydration, reduces itching and inflammation of the skin, improves skin elasticity, and accelerates epidermal wounds' rate of healing.[3] For this purpose, it is sometimes combined with allantoin. D-Pantenol binds to the hair shaft readily; so, it is a common component of commercial shampoos and hair conditioners (in concentrations of 0.1–1%). D-Pantenol coats the hair and seals its surface,[citation needed] lubricating the hair shaft and giving it a shiny appearance. D-Pantenol is also recommended by tattoo artists as a post-tattooing moisturising cream. Adverse effects D-Panthenol is generally well tolerated. In rare cases, skin irritation and contact allergies have been reported.[2][3] Pharmacology D-Panthenol readily penetrates into the skin and mucous membranes (including the intestinal mucosa), where it is quickly oxidized to pantothenic acid. Pantothenic acid is extremely hygroscopic,[4] that is, it binds water effectively. It is also used in the biosynthesis of coenzyme A, which plays a role in a wide range of enzymatic reactions and thus in cell growth.[2][3] Physical and chemical properties Dexpanthenol D-Panthenol is an odourless, slightly bitter, highly viscous, transparent and colourless liquid at room temperature,[5] but salts of pantothenic acid (for example sodium pantothenate) are powders (typically white). D-Pantenol is easily soluble in water and alcohol, moderately soluble in diethyl ether, soluble in chloroform (1:100),[5] in propylene glycol, and slightly soluble in glycerin. D-Panthenol's expanded chemical formula is HO–CH2–C(CH3)2–CH(OH)–CONH–CH2CH2CH2–OH. Stereochemistry D-Panthenol comes in two enantiomers, D and L. Only D-panthenol (dexpanthenol) is biologically active, however both forms have moisturizing properties. For cosmetic use, panthenol comes either in D form, or as a racemic mixture of D and L (DL-panthenol). In cosmetics, panthenol is a humectant, emollient and moisturizer. D-Panthenol binds to hair follicles readily and is a frequent component of shampoos and hair conditioners (in concentrations of 0. 1-1%). D-Panthenol coats the hair and seals its surface, lubricating follicles and making strands appear shiny. Panthenol is the alcohol analog of pantothenic acid (vitamin B5), and is thus the provitamin of B5. In organisms it is quickly oxidized to pantothenate. Panthenol is a viscous transparent liquid at room temperature, but salts of pantothenic acid (for example sodium pantothenate) are powders (typically white). D-Panthenol is well soluble in water, alcohol and propylene glycol, soluble in ether and chloroform, and slightly soluble in glycerin. Overview If you looked around your home, you’d likely run across panthenol in several ingredients lists of products you own. Panthenol appears in food, supplements, and hygienic products of a wide variety. D-Panthenol has a similar chemical structure to alcohol. D-Panthenol’s used to help hydrate and smooth your skin and hair from the inside in its ingestible form and from the outside in its topical form. But is D-Panthenol safe for you and your family when it appears in personal care products? Read on to find out why panthenol is in so many cosmetics and read the facts to understand how it affects your body. What is d-panthenol? d-Panthenol is a chemical substance made from pantothenic acid, also known as vitamin B-5. D-Panthenol occurs organically and can also be produced from both plant and animal sources. D-Panthenol’s used as an additive in various cosmetic products around the globe. You very likely have pantothenic acid in your system right now, since it occurs in so many common food sources. And you’ve likely used a cosmetic or personal care product with D-Panthenol within the last 24 hours. D-Panthenol takes the form of either a white powder or a transparent oil at room temperature. You will sometimes see panthenol listed under one of its other names on ingredients list, including: dexpanthenol D-pantothenyl alcohol butanamide alcohol analog of pantothenic acid provitamin B-5 When absorbed into the body, panthenol becomes vitamin B-5. What’s D-Panthenol used for? In topical cosmetics, product manufacturers often use panthenol as a moisturizer. But D-Panthenol’s also included in many cosmetics as a softening, soothing, and anti-irritant agent.D-Panthenol also helps your skin build up a barrier against irritation and water loss. Skin products Vitamin B-5 is essential for a healthy diet, skin, and hair. D-Panthenol makes sense that panthenol, its derivative, is a staple of many skin care products, such as lotions and cleansers. D-Panthenol’s also found in cosmetics as various as lipstick, foundation, or even mascara.D-Panthenol also appears in creams made to treat insect bites, poison ivy, and even diaper rash. The National Center for Biotechnology Information lists panthenol as a skin protectant with anti-inflammatory properties. D-Panthenol can help improve skin’s hydration, elasticity, and smooth appearance. D-Panthenol also soothes: red skin inflammation little cuts or sores like bug bites or shaving irritation D-Panthenol helps with wound healing, as well as other skin irritations like eczema. Hair products Hair care products include D-Panthenol because of its ability to improve your hair’s: shine softness strength D-Panthenol can also help protect your hair from styling or environmental damage by locking in moisture. One study found that panthenol may help slow down and hide the look of thinning hair. The study tested it with other active ingredients as a leave-in treatment. Nail products Your nails are made from keratin proteins, just like your hair. So, D-Panthenol follows that panthenol can strengthen your finger- and toenails. You might find it in your shine and strengthening nail treatments, or in hand creams and cuticle oils. One study found that applying panthenol to the nail can help hydrate the nail and prevent breakage. Molecular Weight of Panthenol: 205.25 g/mol Computed by PubChem 2.1 (PubChem release 2019.06.18) XLogP3-AA of Panthenol: -0.9 Computed by XLogP3 3.0 (PubChem release 2019.06.18) Hydrogen Bond Donor Count of Panthenol: 4 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Hydrogen Bond Acceptor Count of Panthenol: 4 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Rotatable Bond Count of Panthenol: 6 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Exact Mass of Panthenol: 205.131408 g/mol Computed by PubChem 2.1 (PubChem release 2019.06.18) Monoisotopic Mass of Panthenol: 205.131408 g/mol Computed by PubChem 2.1 (PubChem release 2019.06.18) Topological Polar Surface Area of Panthenol: 89.8 Ų Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Heavy Atom Count of Panthenol: 14 Computed by PubChem Formal Charge of Panthenol: 0 Computed by PubChem Complexity of Panthenol: 182 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Isotope Atom Count of Panthenol: 0 Computed by PubChem Defined Atom Stereocenter Count of Panthenol: 0 Computed by PubChem Undefined Atom Stereocenter Count of Panthenol: 1 Computed by PubChem Defined Bond Stereocenter Count of Panthenol: 0 Computed by PubChem Undefined Bond Stereocenter Count of Panthenol: 0 Computed by PubChem Covalently-Bonded Unit Count of Panthenol: 1 Computed by PubChem Compound of Panthenol Is Canonicalized Yes
PANTHENOL
Panthenol is a chemical substance made from pantothenic acid, also known as vitamin B-5.
Panthenol is made from vitamin B5, also known as pantothenic acid which is found in all living things.
Panthenol is an odorless, transparent, highly viscous, and colorless liquid at room temperature.


CAS Number: 81-13-0 / 16485-10-2
EINECS/ELINCS Number: 201-327-3 / 240-540-6
MDL number: MFCD00065006
Chemical formula: C9H19NO4


Panthenol is a compound that's structurally similar to vitamin B5, or pantothenic acid.
Panthenol's also known as provitamin B5 because it converts into vitamin B5 in the skin.
Chemically, pantothenol is an alcohol, which means it has a hydroxyl group (an oxygen and a hydrogen bonded together).


This hydroxyl group is what makes panthenol different from pantothenic acid.
Panthenol, also known as pro-vitamin B5, is the precursor of vitamin B5 (pantothenic acid, which is a natural constituent of the hair).
Panthenol's name comes from the Greek “pantothen” which means “everywhere”.


Vitamin B5 is found throughout living organisms.
In particular, it plays a role in the development and proper functioning of the central nervous system.
Panthenol is found in certain foods such as meat, fish, egg yolk, almonds and nuts.


Panthenol is a stable form of vitamin B5.
Panthenol is known for its moisturising, soothing and repairing properties.
Panthenol is water soluble and “plays well” with many different types of ingredients, making it easy to formulate with for moisturizers, serums, toners, etc.


As a raw material, two forms of panthenol can be incorporated in personal care product formulas: D-panthenol is a viscous oil and DL-panthenol comes in the form of a white, crystalline powder.
According to the Cosmetic Ingredient Review assessment from 2018, the highest reported concentration of panthenol in a personal care product was 5.3%, which was deemed safe in its use.


Panthenol is a compound found naturally in humans and can also be obtained from plants and animals, with positive effects on the skin.
Panthenol can be obtained from vitamin B5 or pantothenic acid. Panthenol is an important compound for its benefits to the skin.
Panthenol can be found in many cosmetic products such as conditioner, shampoo, shower gel, hair and body moisturizer, face cream, foundation, lipstick, under eye concealer.


In the ingredient list of these products, you can see that D-Panthenol, DL-Panthenol, dexpanthenol, D-Pantothenyl alcohol, butanamide or provitamin B5 are written.
After Panthenol is applied to the body with various products, it is absorbed by the skin and then turns into the form of vitamin B5.
Panthenol comes in two enantiomers: D, and L. Only D-panthenol (dexpanthenol) is biologically active. For cosmetic use, panthenol comes either in D form or as a racemic mixture of D and L (DL-panthenol).


Panthenol speeds up cell turnover and stimulates fibroblasts in the skin.
This is crucial for wound healing, as fibroblasts are necessary for creating structural skin proteins like collagen and elastin.
These proteins are key for facilitating proper tissue repair and wound closure—and ultimately, happy skin.


Panthenol is an alcohol analog of pantothenic acid (Vitamin B5), and thus a provitamin of B5.
Panthenol (also called pantothenol) is the alcohol analog of pantothenic acid (vitamin B5), and is thus a provitamin of B5.
In organisms, Panthenol is quickly oxidized to pantothenic acid.


Panthenol is a viscous transparent liquid at room temperature.
Panthenol occurs organically and can also be produced from both plant and animal sources.
Panthenol takes the form of either a white powder or a transparent oil at room temperature.


You will sometimes see panthenol listed under one of its other names on ingredients list, including:
*dexpanthenol
*D-pantothenyl alcohol
*butanamide
*alcohol analog of pantothenic acid
*provitamin B-5
When absorbed into the body, panthenol becomes vitamin B-5.



USES and APPLICATIONS of PANTHENOL:
Panthenolis used in pharmaceutical and cosmetic products for its benefits for dry, damaged and sensitive skin.
Panthenol is recommended for people with skin problems such as eczema and is very well tolerated, even by the most sensitive skin.
Panthenol is a well-known active ingredient for treating diaper rash in babies and mild burns.


Panthenol is also used for hair and scalp care.
Panthenol is capable of binding to the hair surface.
In a shampoo and conditioner routine, Panthenol is deposited on the hair and thus protects the fiber.


Panthenol has also been shown to repair damaged hair and reduce the damage caused by excessive brushing.
Panthenol also has a humectant (wetting) property.
We use panthenol in our face and body care products, for its moisturising, soothing and repairing properties, and for all skin types, even the most sensitive.


We use Panthenol in makeup, specifically mascara, to strengthen the lashes and give them shine.
Panthenol is also used in the composition of our complexion products for the same benefits as in skin care.
We use Panthenol in haircare products for its moisturising efficiency as it helps to protect the hair and skin on the scalp.


Hair that is dehydrated or low in moisture can benefit from moisturizing properties of panthenol.
Panthenol is used as an emollient, panthenol is also good for rough textured hair because it can smooth out the imperfections in the hair shaft.
Panthenol (sometimes referred to as pro-vitamin B5) is a popular humectant in personal care products due to its ability to attract and hold moisture.


When topically applied, Panthenol converts to pantothenic acid, which is a naturally occurring substance within the body.
Research also shows promise for panthenol’s ability to reduce sensitivity-induced redness in skin.
Topically applied panthenol in amounts between 1-5% has been reported to aid in healing and barrier repair.


It’s important to clarify that even though panthenol is the alcohol derivative of pantothenic acid, but it is a completely gentle and non-drying form of alcohol, unlike SD or denatured alcohol, which are known to be damaging to skin.
Panthenol is also widely used in hair care products and can be found in makeup products, such as powders, mascara, and lipstick.


Panthenol is a precursor of pantothenic acid (or vitamin B5), a key ingredient in many skincare cosmetics in recent years.
Panthenol is a humectant meaning it holds and binds water, and these properties mean that it is ideal when it comes to keeping water in the skin.
Panthenol also works as an emollient which means it can moisturize and soothe the skin, as well as help, protect it from environmental factors and skin stresses.


Panthenol, on the other hand, is frequently added to personal products due to its effects on the skin.
Panthenol's usually used in the form of a transparent viscous liquid, but it can also be used as a white powder.
You can find panthenol listed on labels as pantothenol, D-pantothenol alcohol, dexpanthenol, or provitamin B5.


Panthenol is used as a moisturizer and humectant in cosmetics and personal care products.
Panthenol is found in lotions, ointments, nasal sprays, eye drops, cleaning solutions for contact lenses, etc.
Panthenol is used as a moisturizer, soothing and softening agent.


Panthenol's main job in skincare products is to moisturise the skin.
Panthenol’s a humectant meaning that it can help the skin to attract water and then hold onto it.
There is also research showing that Panthenol can help our skin to produce more lovely lipids that are important for a strong and healthy skin barrier.


Another great thing about Panthenol is that it has anti-inflammatory and skin protecting abilities.
Research also shows that Panthenol might be useful for wound healing as it promotes fibroblast (nice type of cells in our skin that produce skin-firming collagen) proliferation.


If that wasn’t enough Panthenol is also useful in nail and hair care products.
A study shows that a nail treatment liquide with 2% Panthenol could effectively get into the nail and significantly increase the hydration of it.
Panthenol is used for the hair the hydration effect is also true there.


Panthenol might make your hair softer, and more elastic and helps to comb your hair more easily.
Panthenol is used in pharmaceutical and cosmetic products as a moisturizer and to improve wound healing.
In pharmaceuticals, cosmetics, and personal-care products, panthenol is a moisturizer and humectant, Panthenol is used in ointments, lotions, shampoos, nasal sprays, eye drops, lozenges, and cleaning solutions for contact lenses.


In ointments, Panthenol is used for the treatment of sunburns, mild burns, minor skin injuries, and disorders (in concentrations of up to 2–5%).
Panthenol improves hydration, reduces itching and inflammation of the skin, improves skin elasticity, and accelerates epidermal wounds' rate of healing.
For this purpose, Panthenol is sometimes combined with allantoin.


Panthenol binds to the hair shaft readily, so, it is a common component of commercial shampoos and hair conditioners (in concentrations of 0.1–1%).
Panthenol coats the hair and seals its surface, lubricating the hair shaft and giving it a shiny appearance.
Panthenol is also recommended by tattoo artists as a post-tattooing moisturising cream.


Panthenol is generally well tolerated.
Panthenol’s used as an additive in various cosmetic products around the globe.
You very likely have pantothenic acid in your system right now, since it occurs in so many common food sources.
And you’ve likely used a cosmetic or personal care product with panthenol within the last 24 hours.


-Skin care:
Panthenol improves hydration and elasticity of the skin, reduces itching and inflammation of the skin, improves skin elasticity, and accelerates the rate of healing of wounds. In topical creams, it is found to be in a concentration of 1-5%


-Hair care:
Panthenol binds to the hair shaft readily, so, it is a common component of commercial shampoos and hair conditioners (in concentrations of 0.1-1%).
Panthenol coats the hair and seals its surface, lubricating the hair shaft and giving it a shiny appearance.
Panthenol can also help protect your hair from styling or environmental damage by locking in moisture.


-Nail products
Your nails are made from keratin proteins, just like your hair. So, Panthenol follows that panthenol can strengthen your finger- and toenails.
You might find Panthenol in your shine and strengthening nail treatments, or in hand creams and cuticle oils.


-Pharmacology
Panthenol readily penetrates into the skin and mucous membranes (including the intestinal mucosa), where it is quickly oxidized to pantothenic acid.
Pantothenic acid is extremely hygroscopic.
Panthenol is also used in the biosynthesis of coenzyme A, which plays a role in a wide range of enzymatic reactions and in cell growth.



WHAT IS PANTHENOL USED FOR?
In topical cosmetics, product manufacturers often use panthenol as a moisturizer.
But Panthenol’s also included in many cosmetics as a softening, soothing, and anti-irritant agent.
Panthenol also helps your skin build up a barrier against irritation and water loss.

-Skin products:
Vitamin B-5 is essential for a healthy diet, skin, and hair.
Panthenol makes sense that panthenol, its derivative, is a staple of many skin care products, such as lotions and cleansers.
Panthenol’s also found in cosmetics as various as lipstick, foundation, or even mascara.
Panthenol also appears in creams made to treat insect bites, poison ivy, and even diaper rash.

The National Center for Biotechnology Information lists panthenol as a skin protectant with anti-inflammatory properties.
Panthenol can help improve skin’s hydration, elasticity, and smooth appearance.
-Panthenol also soothes:
*red skin
*inflammation
*little cuts or sores like bug bites or shaving irritation
*Panthenol helps with wound healing, as well as other skin irritations like eczema.

-Hair products:
Hair care products include panthenol because of its ability to improve your hair’s:
*shine
*softness
*strength

Panthenol can also help protect your hair from styling or environmental damage by locking in moisture.
Panthenol may help slow down and hide the look of thinning hair.
Panthenol is used with other active ingredients as a leave-in treatment.



HOW TO USE PANTHENOL?
Panthenol has positive effects on body and hair care.
Panthenol is important to get enough from food to maintain the body's energy balance.
If foods containing vitamin B5 are not consumed enough, nutritional supplements and creams containing panthenol can be supported.
Panthenol can be used in cream form by applying it on the skin.
Creams can start to show their effect by being absorbed from the skin in a short time.
Panthenol can also be taken into the body through nutritional and vitamin supplements.



IS PANTHENOL A SAFE SUBSTANCE?
Panthenol can be safely taken into the body topically (application on the skin) and through nutritional supplements.
Panthenol is a compound that can be beneficial for the body if the person does not have any known allergic conditions to vitamin B5 and is used at normal levels.

Both the U.S. Food and Drug Administration (FDA) and the European Commission on Cosmetic Ingredients have approved Panthenol for use in cosmetics.
The National Institutes of Health (NIH) classifies panthenol as “possibly safe” for general topical applications and nasal sprays.
And Panthenol’s listed as “likely safe” for topical use by children.

The FDA currently lists panthenol in its widely known “Generally Regarded as Safe” database for when Panthenol’s ingested as a food ingredient, or as a supplement.
But remember that ingesting Panthenol or panothenic acid in food or as a supplement is very different than using it on your skin or hair.
Although Panthenol’s widely considered beneficial as a supplement, it’s only classified as “likely safe” for topical use on the skin, hair, and nails.



WHAT DOES PANTHENOL DO?
Panthenol can help skin and hair feel better.
Panthenol moisturizes the skin and gives vitality to the hair.
Thanks to its healing power, Panthenol can reduce hair breakage.

Panthenol can provide softness and resistance to the hair.
Panthenol can make hair styling easier by trapping moisture in the hair.
Thus, Panthenol helps to protect the hair from the negative effects of the environment.
In addition to these, Panthenol can help strengthen the fingernails and toenails.

Thus, you can have healthier and break-resistant nails.
Thanks to its positive effects on skin, hair and nails, panthenol can be included in many cosmetic products.
With aging, the skin loses its elasticity by losing moisture.
Panthenol can protect the moisture balance in the skin and cause the negative effects of aging to appear later.



WHAT DOES PANTHENOL DO FOR THE SKIN?
Here's why skin care brands use panthenol in their formulas:

1.
Panthenol acts as a moisturizer.
Panthenol primarily functions as a moisturizer.
Panthenol is a liquid at room temperature, so it's used as a humectant and emollient in skin care products.
(Humectants attract moisture, while emollients fill in cracks with lipids.)

This reduces water loss, keeping the skin soft and smooth.
Panthenol also restores and protects the skin barrier, which is essential for managing general dryness and skin sensitivity.
Scientists are still learning how Panthenol exactly works, but they think its role in enzymatic processes—which is vital for skin barrier function—plays a part.


2.
Panthenol reduces inflammation.
As Panthenol converts into pantothenic acid (which then makes coenzyme A), it also helps decrease inflammation.
That's because coenzyme A is necessary for the production of steroids and fatty acids, which soothe inflammation.
This anti-inflammatory effect makes Panthenol useful for alleviating symptoms of skin irritation, including itching, scaling, dryness, and roughness.
In fact, many sunscreens and after-sun products contain panthenol for this reason.


3.
Panthenol supports wound healing.
By mediating inflammation, panthenol can also help the wound healing process.
Panthenol's been shown to decrease erythem, or skin reddening, when applied to wounds in the top layer of the skin.
Panthenol's ability to attract moisture (and control water loss) also encourages skin regeneration, further supporting wound recovery.



BENEFITS OF PANTHENOL FOR HAIR:
Panthenol is a natural humectant and emollient, experts agree that panthenol has multiple benefits for use in hair.
*Retains moisture:
Panthenol is a desirable skincare and haircare ingredient because it acts as a humectant, drawing in moisture.
Panthenol draws moisture from the environment and skin to where it is needed most.

*Smooths strands:
Panthenol acts as an emollient, smoothing cracks in rough skin and hair.
Panthenol is also good for rough textured hair because it can smooth out the imperfections in the hair shaft.

*Panthenol acts as an anti-inflammatory:
Panthenol in the body is converted to vitamin B5, which has anti-inflammatory properties that aid in the reparative process of damaged hair.

*Panthenol can help with thinning hair:
a study looking to treat thinning hair, panthenol showed as a promising ingredient to help contribute to help to mitigate the effects of thinning hair, and D-panthenol showed an increase in cell viability, supporting hair growth stimulation.

*Balances:
Panthenol can also help balance hair's moisture content to improve condition and suppleness and is a brilliant emollient, which also helps to improve hair's suppleness.

*Strengthens:
Panthenol is a strengthening agent that penetrates deep into the cortex.

*Hair Type Considerations:
The experts agree that Panthenol generally works for most hair types, making it a great universal ingredient in hair care.
Safe to use daily, Panthenol's often found in hair products across the board, including shampoo, conditioner, and leave-in product.



WHAT ARE THE PRODUCTS CONTAINING PANTHENOL?
Panthenol can be found in many commonly used skin and hair care products.
Panthenol can be found in the content of cosmetic products such as make-up.
In addition to these products, Panthenol can also be used in the manufacture of prescription and over-the-counter drugs.
Some of the products containing panthenol are:

*Hair Care Products:
Hair care products can be important for maintaining the health of the hair.
Panthenol can be found in products such as shampoo, conditioner, hair moisturizer, hair mousse, hair spray. Panthenol can nourish and moisturize the hair.
Panthenol may have benefits such as removing the lifelessness of the hair and giving fullness to the hair.

*Skin care products:
Panthenol can be found in personal care products such as face cream, skin moisturizer, tonic, eye cream, sunscreen, make-up removers, shaving foam.
Panthenol provides moisture to the skin and may support wound healing.

*Cosmetics:
Panthenol can be found in make-up materials such as mascara, foundation, eyeliner, lipstick, powder and fixer that can be used every day.

*Mother and Baby Products:
Since mother and baby products are applied to sensitive skin, the ingredients must be reliable.
Panthenol can be found in many products such as baby shampoo, soap, and lotion.



BENEFITS OF PANTHENOL:
*Panthenol moisturizes the skin
Panthenol makes for a great moisturizing ingredient.
Research has shown that it decreases transepidermal water loss (water that evaporates through the skin).
Products containing just 1% of panthenol can rapidly hydrate skin, resulting in a more supple feel and appearance.

This means that panthenol is ideal for skin types that are experiencing particularly stressful environmental factors, such as harsh climates, air conditioning, or central heating.
Panthenol’s ability to combat transepidermal loss makes it perfect for dealing with the stresses that these types of factors cause.

*Panthenol helps maintain the skin’s barrier:
Panthenol’s emollient properties help to maintain a healthy skin barrier.
Your skin barrier consists of natural oils and lipids that Panthenol protects your skin from water loss, allergens, and bacteria.



WHAT ARE THE PANTHENOL BENEFITS TO THE SKIN?
Panthenol is a substance that stands out with its benefits.
Panthenol can contribute to the healing of tissues such as skin, hair, eyes, nose and nails.
Panthenol can be added to the content of personal care products due to its moisturizing and skin soothing effects.
The benefits of Panthenol to the skin can be listed as follows:

*Can Remove Wrinkles Caused by Aging:
As age progresses, the moisture of the skin decreases and the tissues begin to sag.
In addition, the lines on the skin increase and may deepen.
As the skin loses Panthenol's elasticity, the effects of aging begin to be seen.
Panthenol restores the skin's natural moisture.
Thus, the elasticity of the skin increases and a smooth appearance can be achieved.

*May Contribute to Tissue Repair by Accelerating Wound Healing:
One of the contributions of Panthenol for the skin is that it supports tissue repair.
Panthenol may also contribute to the healing of skin diseases such as eczema.

*May Prevent Water Loss by Moisturizing the Skin:
The skin may lose moisture due to aging, environmental factors, and the harmful effects of sun rays.
As a result, delay in wound healing and various skin diseases may occur.
In order to maintain the moisture balance of the body, Panthenol is necessary to get enough vitamin B5 to the body by eating a healthy diet.
Panthenol may have a healing effect in skin diseases such as dry skin, atopic dermatitis, and psoriasis.

*May Protect Tissues Thanks to Its Anti-Inflammatory Properties:
Inflammatory conditions may occur due to skin injuries, sunburn, irritation.
Panthenol, which has anti-inflammatory properties, can act as a barrier by protecting the skin.
Panthenol can increase fat synthesis and new cell formation in the skin.
Thus, Panthenol can help reduce problems such as itching, redness, and dryness.



WHAT DOES PANTHENOL DO FOR THE SKIN?
Panthenol’s molecular structure and chemical properties mean that it is rejuvenating and benefits a number of different skin issues.



WHAT ARE THE PANTHENOL BENEFITS?
Panthenol is a substance produced from vitamin B5 (pantothenic acid) that contributes to the moisture balance of the body.
Panthenol occurs naturally in humans as well as in plants and animals.
Panthenol can also be included in the content of skin and hair care products and make-up materials.
Panthenol is a prominent compound due to its tissue repair, wound healing and anti-inflammatory properties.
In addition to these advantages, Panthenol is also beneficial for nail health.



HOW TO USE PANTHENOL FOR HAIR:
Panthenol is a low-risk ingredient that can be found in many products and may have many uses.
Panthenol is found in many products, which themselves may have specific recommendations on when to use them.



PANTHENOL AT A GLANCE:
*Hydrating ingredient famous for its ability to attract/retain moisture
*Panthenol may also help reduce sensitivity-induced redness in skin
*Often referred to as pro-vitamin B5
*Converts into pantothenic acid when applied topically
*White, crystalline powder in its raw material state



WHERE DOES PANTHENOL COME FROM?
Panthenol is an alcohol of fossil origin.
It is obtained by a process using minimum energy and water.
90% of the waste generated is recycled and recovered, such as calcium sulphate, which is used in land restoration.
Panthenol has an excellent environmental profile and is biodegradable.



WHAT DOES PANTHENOL DO IN A FORMULATION?
*Hair conditioning
*Humectant
*Skin conditioning
*Soothing



PHYSICAL AND CHEMICAL PROPERTIES OF PANTHENOL:
Panthenol is an odourless, slightly bitter, highly viscous, transparent, and colourless liquid at room temperature, but salts of pantothenic acid (for example sodium pantothenate) are powders that are typically white.
Panthenol is easily soluble in water and alcohol, moderately soluble in diethyl ether, soluble in chloroform (1:100), in propylene glycol, and slightly soluble in glycerin.
Panthenol's expanded chemical formula is HO–CH2–C(CH3)2–CH(OH)–CONH–CH2CH2CH2–OH.



STEREOCHEMISTRY OF PANTHENOL:
Panthenol comes in two enantiomers: D, and L. Only D-panthenol (dexpanthenol) is biologically active, however both forms have moisturizing properties.
For cosmetic use, panthenol comes either in D form, or as a racemic mixture of D and L (DL-panthenol).



PHYSICAL and CHEMICAL PROPERTIES of PANTHENOL:
Chemical formula: C9H19NO4
Molar mass: 205.254 g·mol−1
Appearance: Highly viscous, colourless liquid
Density: 1.2 g mL−1 (at 20 °C)
Melting point: 66 to 69 °C (151 to 156 °F; 339 to 342 K)[contradictory]
Boiling point: 118 to 120 °C (244 to 248 °F; 391 to 393 K) at 2.7 Pa
log P: −0.989
Acidity (pKa): 13.033
Basicity (pKb): 0.964
Chiral rotation: ([α]D) +29° to +30°
Refractive index: (nD) 1.499
Physical state: solid
Color: white
Odor: No data available
Melting point/freezing point:
Melting point/range: 66 - 69 °C - lit.
Initial boiling point and boiling range: No data available

Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: No data available
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: No data available
Partition coefficient: n-octanol/water: No data available
Vapor pressure: No data available
Density: No data available
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: No data available
Other safety information: No data available



FIRST AID MEASURES of PANTHENOL:
-Description of first-aid measures:
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Remove contact lenses.
*If swallowed:
After swallowing:
Make victim drink water (two glasses at most).
Consult doctor if feeling unwell.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of PANTHENOL:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of PANTHENOL:
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of PANTHENOL:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection tested.
Safety glasses
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of PANTHENOL:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
Hygroscopic.



STABILITY and REACTIVITY of PANTHENOL:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available



SYNONYMS:
2,4-Dihydroxy-N-(3-hydroxypropyl)-3,3-dimethylbutanamide[1]
Pantothenol
Pantothenyl alcohol
N-Pantoylpropanolamine
Bepanthen (trade name)
Dexpanthenol (D form)
DL-Pantothenyl alcohol
(±)-2,4-Dihydroxy-3,3-dimethylbutyric 3-hydroxypropylamide
(±)-α,γ-Dihydroxy-N-(3-hydroxypropyl)-β,βdimethylbutyramide

PAPEMP
Polyamino polyether methylene phosphonic acid(PAPEMP Acid) , Polyoxypropylenediaminetetramethylenephosphonic acid,Mayoquest 2200 CAS No. : 130668–24–5
PAPEMP
Polyamino Polyether Methylene Phosphonic Acid PAPEMP Polyamino Polyether Methylene Phosphonate Molecular weight: about 600 PAPEMP Acid- Polyamino polyether methylene phosphonic acid PAPEMP (Polyamino Polyether Methylene Phosphonate) Properties: PAPEMP performs excellently in the condition of high hardness and pH as a new antiscalant and corrosion inhibitor. With high calcium tolerance, PAPEMP scale inhibition ability is also high, particularly for CaCO3, CaPO4, and CaSO4. It also effectively restrain the Si scale from a formation and stabilize the ions. Such as Mn, and Fe to form chelating compounds. PAPEMP also has a good tolerance to high temperature, high turbidity, high salt concentration, and high chlorine (Cl– and Br–) concentration. PAPEMP can be used as scale and corrosion inhibitor in circulating cool water system and oilfield refill water system in situations of high hardness, high alkali, and high pH value. PAPEMP can be used as a scale inhibitor for a reverse osmosis system and a multistep flash vaporization system. PAPEMP can significantly inhibit calcium carbonate precipitation from the aqueous solution by modifying the crystal morphology Structural Formula: CH2(OCH2CH)nCH3NCH2CH2P(OH)2P(OH)2OOHCCH3NCH2CH2(HO)2P(HO)2POO Properties: PAPEMP is a new kind of water treatment agent. PAPEMP has high chelation and dispersion effects, high value of calcium tolerance, and good scale inhibition effects. PAPEMP can be used as scale and corrosion inhibitor in circulating cool water system and oilfield refill water system in situations of high hardness, high alkali and high pH value. PAPEMP has excellent scale inhibition ability to calcium carbonate, calcium sulfate and calcium phosphate. PAPEMP can efficiently inhibit the formation of silica scale, stabilize metal ions such as Zn, Mn and Fe. PAPEMP can be used as scale inhibitor for reverse osmosis system and multistep flash vaporization system in which high salt concentration, high turbidity and high temperature are usually encountered (such as high temperature and high turbidity in coal vaporization system), accessory agent for woven & dyeing (for example, yellow turnback inhibition agent), as alternatives of EDTA, DTPA and NTA. CAS No. : 130668–24–5 Polyamino polyether methylene phosphonate (PAPEMP) is very effective in preventing calcium carbonate precipitation at high supersaturation and high pH. The inhibition of calcium carbonate crystallization in the presence of PAPEMP at both low and high supersaturation was studied and then compared to the inhibitory ability of hydroxyethylidene-1 ,1-diphosphonic acid (HEDP). Keywords: calcium carbonate inhibition, crystallization kinetics, phosphonates, affinity constants, calcium tolerance. PAPEMP is a new kind of water treatment agent. PAPEMP has high chelation and dispersion effects, high value of calcium tolerance, and good scale inhibition effects. PAPEMP is as scale and corrosion inhibitor in circulating cool water system and oilfield refill water system in situations of high hardness, high alkali and high pH value. PAPEMP inhibits scale formation of calcium carbonate, calcium sulfate and calcium phosphate. Polyamino Polyether Methylene Phosphonic Acid is a new kind of water treatment agent. PAPEMP has high chelation and dispersion effects, high value of calcium tolerance, and good scale inhibition effects. Polyamino Polyether Methylene Phosphonic Acid can be used as scale and corrosion inhibitor in circulating cool water system and oilfield refill water system in situations of high hardness, high alkali and high pH value. Polyamino Polyether Methylene Phosphonic Acid has excellent scale inhibition ability to calcium carbonate, calcium sulfate and calcium phosphate. Polyamino Polyether Methylene Phosphonic Acid can efficiently inhibit the formation of silica scale, stabilize metal ions such as Zn, Mn and Fe. Polyamino Polyether Methylene Phosphonic Acid can be used as scale inhibitor for reverse osmosis system and multistep flash vaporization system in which high salt concentration, high turbidity and high temperature are usually encountered (such as high temperature and high turbidity in coal vaporization system), accessory agent for woven & dyeing (for example, yellow turnback inhibition agent), as alternatives of EDTA, DTPA and NTA. PAPEMP is a new kind of scale inhibitor for industrial water treatment. PAPEMP has high chelation and dispersion effect with high value of calcium tolerance and scale inhibition effect. PAPEMP can be used as scale and corrosion inhibitor in circulating cooling water system and oilfield of high hardness including calcium magnesium and barium sulfate scale inhibitor. PAPEMP is stable in aqueous solution under a wide range of pH, temperature and pressure. Polyamino polyether methylene phosphonate widens the operational conditions available with today’s standard technology by allowing operations with hard water at higher pH levels and greater salt concentrations. PAPEMP it is possible to operate at up to 300X calcite saturation because of its excellent calcium tolerance. As a result it controls up to three times as much calcium carbonate as ATMP or PBTC (operating at up to 100x calcite saturation). Applications: · PAPEMP has excellent scale inhibition ability to calcium carbonate, calcium sulfate and calcium phosphate. · PAPEMP can efficiently inhibit the formation of silica scale,stabilize metal ions such as Zn, Mn and Fe. It effectively chelates metal ions including calcium, magnesium, iron and copper. · PAPEMP can be used as scale inhibitor for reverse osmosis system and multi-step flash vaporization system in which high salt concentration, high turbidity and high temperature are usually encountered (such as high temperature and high turbidity in coal vaporization system), accessory agent for woven & dyeing (for example, yellow turn back inhibition agent), as alternatives of EDTA, DTPA and NTA . Synonyms: · PAPEMP · Polyoxypropylenediaminetetramethylenephosphonic acid Product Use : Scale and corrosion inhibitor intermediate Chemical Name : Polyamino Polyether Methylene Phosphonic Acid Appearance: Amber transparent liquid Solid content %: 45.0min Active component (PAPEMP) %: 40.0min Phosphoric acid (as PO43-)%: 1.0max Density (20℃)g/cm3: 1.20±0.05 pH(1% solution): 2.0±0.5 Usage: The dosage of 5-100mg/L is preferred. Different from other water treatment agents, the more quantity is, the better the effect. PAPEMP can be used with polycarboxylic acids. Package and Storage: Normally In 250kg net Plastic Drum, IBC drum can also be used as required. Storage for ten months in room shady and dry place. The new calcium carbonate inhibitor is PolyAmino PolyEther Methylene Phosphonate2 (PAPEMP). One of the particular advantages of the PAPEMP molecule is its exceptional calcium tolerance (Table 2). Calcium tolerance is a measure of a chemical compound’s ability to remain soluble in the presence of calcium ions (Ca2+) under both high pH and high temperature, such as in geothermal brines. As pH and temperature increases, calcium tolerance decreases rapidly for traditional CaCO3 threshold inhibitors (as shown in Figure 1), e.g., 1-hydroxy ethylidene 1,1-diphosphonic acid (HEDP), amino tri (methylene phosphonic acid) (AMP), and polyacrylic acid. The X-axis in this figure is the amount of HEDP as PPM needed to form precipitation in a water containing 10,000 PPM of Calcium ions. The data for temperature curve was collected at pH 9, while the pH curve represents data at 250°F. At higher temperature and/or higher pH, it requires Poly amino polyether methylene phosphonate (PAPEMP) is a very effective inhibitor in preventing CaCO3 precipitation. The extraordinary affinity of PAPEMP towards CaCO3 surfaces and its excellent tolerance of calcium materials make this polymer excellent in inhibiting the growth of CaCO3 crystal. Amjad et al. have extensively studied phosphonate-based polymer performance in cold water. They have studied the effectiveness of phosphate and phosphonate polymers in stabilized and all-organic cooling water treatment facilities. This study reported that these polymers are capable of performing a dual function. Firstly, they control the thickness of the calcium phosphate and phosphonate membrane on the metal surface. Secondly, they prevent the precipitation of the calcium phosphate and phosphonate salts in the recirculating water. Another study conducted by the same research group demonstrated the performance of sulphonic-acid-containing terpolymer for controlling the growth of calcium phosphonates and carbonate scale. It showed that these polymers improved the control of calcium phosphonate and carbonate in highly stressed cooling water systems [28]. Wang et al. also conducted a similar study in which they have reported the inhibition of CaCO3 by a phosphonate-terminated poly(maleic-co-sulfonate) polymeric inhibitor. This study showed that this inhibitor is capable of controlling CaCO3 scale Polyamino Polyether Methylene Phosphonate (PAPEMP) Investigation of CaCO3 scale inhibition by PAA, ATMP and PAPEMP Calcium carbonate scale inhibition by three inhibitors, polyacrylic acid (PAA), aminotrimethylenephosphonic acid (ATMP) and polyamino polyether methylenephosphonate (PAPEMP), has been investigated by the bubbling method, and the calcium carbonate scales formed in the absence and presence of inhibitors have been examined by SEM and XRD. It was found that ATMP shows “threshold effect” in the inhibition of CaCO3 scale, and the inhibition behavior of PAPEMP is similar to that of PAA: the “threshold effect” is not observed. In the presence of inhibitors, the normal growth of calcium carbonate is disturbed, and in the presence of PAPEMP, the scale morphology is similar to that in the presence of ATMP. The vaterite phase is effectively stabilized kinetically in the presence of PAA; ATMP takes second place, and PAPEMP can hardly stabilize kinetically the vaterite phase In recent years, the percentage of oil production from more challenging environments has increased. In addition to the numerous engineering and logistical difficulties of working at increased depth, temperature and pressure these production zones provide a harsh environment deleterious to the performance of some critical oilfield chemicals. Scale inhibitors are one class of oil field chemicals which are deployed through squeeze treatments into the formation and/or continuous downhole injection for protection of production tubulars. As well depths continue to increase, the exposure time of the injected chemicals also increases. With temperatures in the range of 180-200 °C and pressures exceeding 10,000 psi, the effect of elevated temperature and pressure on scale inhibitor performance is a critical parameter to evaluate using chemical analytical techniques and product performance methods. Another trend leading to increased thermal exposure is the use of thermal enhanced recovery techniques. Scale inhibitors are exposed to high temperatures in operations such as steam flooding and steam assisted gravity drainage (SAGD). In this study, a range of chemicals have been evaluated for their short and medium-term thermal stability at 180 and 200 °C. The primary application of this data is for downhole injection and squeeze treatments prior to adsorption. Inhibitor chemical types include sulfonated polycarboxylic acid (SPCA), fluorescent tagged sulfonated polycarboxylic acid (FSPCA), phosphorous tagged sulfonated polycarboxylic acid (PSPCA), sulfonated polyacrylocarboxylic acid (SPAC), polyacrylic acid (PAA), polyvinyl sulfonate (PVS), polyamino polyether methylene phosphonate (PAPEMP), bis(hexamethylene)triamine pentakis(methylene phosphonic acid) (BHTPMP) and diethylenetriamine pentakis(methylene phosphonic acid) (DTPMP). In most cases the sodium or potassium salts of the inhibitors are used. The chemical effect of temperature on scale inhibitors is measured through molecular weight determination, thermogravimetric analysis (TGA), pH change, and Fourier Transform Infrared (FTIR) analysis. The performance of these inhibitors is measured under static and dynamic conditions for inhibition of barium sulfate scale. These results help to further the knowledge of inhibitor degradation due to thermal effects and indicate the direction for further product development of thermally stable scale inhibitors. Calcium sulfate dihydrate (gypsum) scale inhibition by PAA, PAPEMP, and PAA/PAPEMP blend Z. Amjad, R. T. Landgraf and J. L. Penn Walsh University, Division of Mathematics and Sciences, North Canton OH 44720, USA Abstract: The effects of poly(acrylic acid), PAA, polyamino polyether methylene phosphonic acid, PAPEMP, and PAA/PAPEMP blend on calcium sulfate dihydrate (gypsum) are reported in this paper. It has been found that gypsum inhibition by PAA increases with increasing PAA concentration. Among the various phoshonates (i.e., aminotris(methylene phosphonic acid), AMP; hydroxyphosphono acetic acid, HPA; hydroxyethylidene 1,1-diphosphonic acid, HEDP; 2-phosphonobutane 1,2,4-tricarboxylic acid, PBTC; and polyether polyamino phosphonic acid, PAPEP) evaluated, PAPEMP shows the best inhibition for gypsum precipitation. It has also been observed that presence of PAPEMP exhibits synergistic effect on the performance of PAA. Results on calcium ion compatibility of various phosphonates show that PAPEMP compared to other phosphonates tested show higher tolerance to calcium ions. Keywords: calcium sulfate dihydrate, precipitation, inhibition, polymer, phosphonates Properties : PAPE is a new kind of water treatment chemicals. PAPE has good scale and corrosion inhibition ability. Because more than one ployethylene glycol group is introduced into the molecular, the scale and corrosion inhibition for calcium scale is improved. PAPE has good inhibition effect for barium and strontium scales. PAPE has good scale inhibition effect for calcium carbonate and calcium sulfate, it can mix well with polycarboxylic acid, organophoronic acid, phosphate and zinc salt. PAPE can be used as scale inhibitor for oilfield (recommended as alternatives of Nalco Visco 953) and industrial cool water system. Deposition of unwanted materials, including mineral scales, suspended matter, microbiological growth, and corrosion products, continues to plague the operation of industrial water systems. This article presents performance data on polyamino polyether methylene phosphonic acid (PAPEMP) on various mineral scales commonly encountered in boiler, cooling, desalination, geothermal, gas, and oil systems. Water that is available for domestic and industrial applications typically contains many impurities. These impurities are generally classified in five broad categories: • Dissolved inorganic compounds (i.e., carbonates, sulfates, phosphates, and fluorides of calcium, magnesium, barium, and strontium; small amounts of copper [Cu], iron [Fe], and manganese [Mn]); and other substances • Dissolved gases (e.g., oxygen [O2], nitrogen [N2], carbon dioxide [CO2], and hydrogen sulfide [H2S]) • Suspended matter (e.g., clay, silt, fat, and oil) • Soluble organic compounds (e.g., humic acid, fulvic acid, and tannic acid) • Microorganisms (e.g., algae, bacteria, and fungi) The accumulation of unwanted deposits on equipment surfaces is a phenomenon that occurs in virtually all processes in which untreated water is heated. The deposition of these materials, especially on heat exchanger surfaces in boiler, cooling, geothermal, and distillation systems, can cause a number of operational problems such as plugged pipes and pumps, inefficient use of water treatment chemicals, increased operational costs, lost production due to system downtime, and ultimately heat exchanger failure. Greater water conservation has been a driver for operating industrial water systems at higher concentration cycles, which increases the potential for deposit buildup on heat exchanger surfaces. Operating industrial water systems under stressed conditions demands a better understanding of the feed and recirculating systems’ water chemistry as well as the development of innovative additives and technological approaches for controlling scale, deposit, corrosion, and biofouling. The most promising scale control method among various approaches involves adding substoichiometric dosages, typically a few ppm, of water-soluble additives to the feedwater. Additives commonly used in water treatment formulation fall into two categories: • Dissolved inorganic compounds (i.e., carbonates, sulfates, phosphates, and fluorides of calcium, magnesium, barium, and strontium; small amounts of copper [Cu], iron [Fe], and manganese [Mn] ions; and other substances) • Polymeric (e.g., homopolymers of acrylic acid, maleic acid, itaconic acid, aspartic acid, and copolymers containing monomers of different functional groups) Although there are many phosphonates available, three of the most commonly used phosphonates in water treatment formulations are aminotrismethylene phosphonic acid (AMP); 1-hydroxyethylidine, 1,-1 diphosphonic acid (HEDP); and 2-phosphono-butane 1,2,4-tricarboxylic acid (PBTC). However, under certain pH, concentration, and temperature conditions, phosphonates have been shown to precipitate in the presence of calcium ions. The precipitation of calcium phosphonate salts not only creates fouling of heat exchanger and reverse osmosis (RO) membrane surfaces, it also decreases the solution concentration of a phosphonate to such an extent that severe calcium carbonate (CaCO3) scaling can occur. The focus of this study is to evaluate the performance of polyamino polyether methylene phosphonic acid (PAPEMP) as an inhibitor for various scales (e.g., CaCO3, calcium sulfate dihydrate [CaSO4•2H2O], and calcium phosphate [Ca3(PO4)2]) and a stabilization agent for Fe(III) or Fe3+ ions. Experimental Protocols All chemicals were obtained from commercial sources. They include AMP, HEDP, PBTC, 2-hydroxyphosphono acetic acid (HPA), PAPEMP, and polyacrylic acid (PAA). Detailed procedures for reagents solution preparation; percent inhibition (%I) calculation for calcium sulfate dihydrate (CaSO4•2H2O), CaCO3, Ca3(PO4)2, and Fe3+ stabilization; and instruments used are reported elsewhere.3-6 Table 1 lists the inhibitors tested. PAPEMP production process consists of 4 steps. Phosphorus acid is input into the reactor and its pH is adjusted by HCl. Polyetheramine is instilled and the reaction starts while the reactor is heated. Formaldehyde is input a few hours later. The reactor will be further heated and steamed for more hours. Usage:The good adaption to different situations enables PAPEMP widely used in boiler, cooling water system and oilfield reinjection water as antiscalant and corrosion inhibitor. For the same reason, PAPEMP is also applied in RO and multistep flash system. Recommend dosage is 5-100 ml/L. Unlike other organophosphonates, there is no optimum dosage for it. Higher the dosage, better the effect. Besides, PAPEMP works as a nutrient absorber in agriculture. It can also replace those more expensive color transfer inhibitors (eg. yellow turnback inhibitor) like EDTA, NTA, and DTPA in textile dyeing. Calcium carbonate scale inhibition by three inhibitors, polyacrylic acid (PAA), aminotrimethylenephosphonic acid (ATMP) and polyamino polyether methylenephosphonate (PAPEMP), has been investigated by the bubbling method, and the calcium carbonate scales formed in the absence and presence of inhibitors have been examined by SEM and XRD. It was found that ATMP shows “threshold effect” in the inhibition of CaCO3 scale, and the inhibition behavior of PAPEMP is similar to that of PAA: the “threshold effect” is not observed. In the presence of inhibitors, the normal growth of calcium carbonate is disturbed, and in the presence of PAPEMP, the scale morphology is similar to that in the presence of ATMP. The vaterite phase is effectively stabilized kinetically in the presence of PAA; ATMP takes second place, and PAPEMP can hardly stabilize kinetically the vaterite phase. Poly-amino poly-ether methylenephosphonic acid (PAPEMP)-containing corrosion and scale inhibitor Abstract The invention provides a poly-amino poly-ether methylenephosphonic acid (PAPEMP)-containing corrosion and scale inhibitor, belongs to the technical field of water treatment and relates to a corrosion and scale inhibitor. The corrosion and scale inhibitor comprises PAPEMP, a zinc salt, a dispersant, a copper corrosion inhibitor and water. The corrosion and scale inhibitor has a reasonable formula, has good use effects and a low production cost, is suitable for an open circulated cooling water system and is especially suitable for a high-hardness, high-basicity and high-pH circulated cooling water system. PAPEMP is excellent to the scale-inhibiting properties of calcium carbonate, calcium phosphate, calcium sulfate, effectively can suppresses the formation of silicon dirt simultaneously, and there is the effect of satisfactory stability metal ion as zinc, manganese, iron. PAPEMP is a new kind of water treatment agent. XF-335S (PAPEMP) has high chelation and dispersion effects, high value of calcium tolerance, and good scale inhibition effects. PAPEMP can be used as scale and corrosion inhibitor in circulating cool water system and oilfield refill water system in situations of high hardness, high alkali and high pH value. PAPEMP has excellent scale inhibition ability to calcium carbonate, calcium sulfate and calcium phosphate. PAPEMP can efficiently inhibit the formation of silica scale, stabilize metal ions such as Zn, Mn and Fe. PAPEMP can be used as scale inhibitor for reverse osmosis system and multistepflash vaporization system in which high salt concentration, high turbidity and high temperature are usually encountered (such as high temperature and high turbidity in coal vaporization system), accessory agent for woven & dyeing, as alternatives of EDTA, DTPA and NTA . Calcium carbonate has been identified as the main problem associated with industrial cooling water scaling or deposition. The formation of calcium carbonate scale in industrial cooling water system has been known to pose significant problems to the industrial processes. The calcium carbonate scales or deposits will serve as a heat insulating layer that reduces heat transfer efficiency and hence require higher energy consumption to attain the desired cooling or heating effect (Prisciandaro et al., 2013). Therefore, it is vital to ensure that heat transfer surfaces on industrial cooling water systems are relatively free from calcium carbonate scaling problems. Most of the research works on crystal growth inhibition of industrial cooling water treatment program were conducted by a few multinational water treatment companies at their own research center. This valuable information is unfortunately not available to others due to trade secret. As such smaller water treatment companies that have limited resources have limited information in developing the right formulation in their cooling water treatment program. This study aims to provide such information so that it can be made available to enhance the technical competency of calcium carbonate scale inhibition. Calcium carbonate crystal growth inhibition by the simplest form of phosphate-containing compounds, orthophosphate, has been well studied by several researchers and orthophosphate concentration in the range of several milligrams per liter have been found to retard the crystal growth in seeded solutions. Adsorption of orthophosphate on calcium carbonate scale has been studied and found to change the structure of calcium carbonate crystal lattice. In another study, CaHPO4 was found to be the responsible species that absorbs on the calcium carbonate surface and inhibits further precipitation. The use of polyphosphates for calcium carbonate crystal growth inhibition was also investigated and sodium tri-polyphosphate was found to be the strongest inhibitor in a mono polyphosphate formulation followed by sodium pyrophosphate and sodium hexametaphosphate. However, orthophosphate and polyphosphates were excluded in this study, driven by market trend towards low or non-phosphorus compounds used for such application in consideration of environmental issues such as eutrophication associated with phosphorus compounds. Calcium carbonate scale inhibition by organophosphorus compounds such as amino tris(methylene phosphonic acid) (ATMP), ethylene-diamine tetra(methylenephosphonic acid) (EDTMP), hexamethylenediamine tetra(methylenephosphonic acid) (HDTMP), diethylenetriamine penta(methylenephosphonic acid) (DTPMP) and PAPEMP were also being investigated. Results shown that the phosphonic group number and the methylene chain length play a vital role in the effectiveness of the inhibitors. Although the application of most organophosphorus compound contributes lesser phosphorus to the environment in relative term to orthophosphate and polyphosphates, some of the commonly used compounds such as ATMP still contains considerable amount of phosphorus (31 % as Phosphorus) and 1-hydroxyethane 1,1-diphosphonic acid (HEDP) (30 % as Phosphorus). Owing to the environmental consideration, this study has selected non-phosphorous polymeric compound represented by PMA and AA/MA copolymer and low phosphorus contributor PAPEMP (about 20 % as Phosphorus) for the tests. The inhibition of calcium carbonate crystal growth by PMA, PAPEMP and AA/MA copolymer was investigated via static beaker tests at typical water chemistries encountered in cooling water system. his study provides a method that enables the evaluation of scale inhibitors at the practical dosage level and economically viable range at various water chemistries encountered in the market place, thus providing a practical and useful solution and background formulation information to water treatment professionals to mitigate industrial cooling water scaling and deposition problems for a given water chemistries and condition. The desired inhibition efficiency of minimum 90 % was set up to evaluate and compare the performance of the above inhibitors.
PARA BENZOQUINONE
PARA BENZOQUINONE

DESCRIPTION:


p-Benzoquinone, also known as para-quinone or 1,4-Benzoquinone, is used as a precursor to hydroquinone.
Ungraded products are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use.

CAS Number: 106-51-4
EC Number: 203-405-2
Molecular Formula: C6H4O2



Para-benzoquinone appears as a yellowish-colored crystalline solid with a pungent, irritating odor.
Para-benzoquinone is Poisonous by ingestion or inhalation of vapors.
Para-benzoquinone May severely damage skin, eyes and mucous membranes.
Para-benzoquinone is Used to make dyes and as a photographic chemical.

Para-benzoquinone is the simplest member of the class of 1,4-benzoquinones, obtained by the formal oxidation of hydroquinone to the corresponding diketone.
Para-benzoquinone is a metabolite of benzene.
Para-benzoquinone has a role as a cofactor, a human xenobiotic metabolite and a mouse metabolite.
Quinone is a metabolite found in or produced by Escherichia coli





p-Benzoquinone (PBQ) is a cyclic conjugated diketone.
Its high-resolution photoelectron spectrum has been reported.
The visible and near ultraviolet spectra of PBQ have been recorded and analyzed.

Its addition as coagent has been reported to enhance the crosslinking rate of polypropylene initiated by the pyrolysis of peroxides.
Its impact on hemoglobin (Hb) has been investigated based on immunoblots and mass spectral analysis of a smoker′s blood

Para-benzoquinone, commonly known as para-quinone, is a chemical compound with the formula C6H4O2.
In a pure state, p-Benzoquinone forms bright-yellow crystals with a characteristic irritating odor, resembling that of chlorine, bleach, and hot plastic or formaldehyde.
This six-membered ring compound is the oxidized derivative of p-Benzoquinone.

The molecule is multifunctional: it exhibits properties of a ketone, being able to form oximes; an oxidant, forming the dihydroxy derivative; and an alkene, undergoing addition reactions, especially those typical for α,β-unsaturated ketones.
Para-benzoquinone is sensitive toward both strong mineral acids and alkali, which cause condensation and decomposition of the compound.

PREPARATION OF PARA -BENZOQUINONE:
p-Benzoquinone is prepared industrially by oxidation of hydroquinone, which can be obtained by several routes.
One route involves oxidation of diisopropylbenzene and the Hock rearrangement.
The net reaction can be represented as follows:

C6H4(CHMe2)2 + 3 O2 → C6H4O2 + 2 OCMe2 + H2O
The reaction proceeds via the bis(hydroperoxide) and the hydroquinone.
Acetone is a coproduct.

Another major process involves the direct hydroxylation of phenol by acidic hydrogen peroxide: C6H5OH + H2O2 → C6H4(OH)2 + H2O Both hydroquinone and catechol are produced.
Subsequent oxidation of the hydroquinone gives the quinone.

Quinone was originally prepared industrially by oxidation of aniline, for example by manganese dioxide.
This method is mainly practiced in PRC where environmental regulations are more relaxed.

Oxidation of hydroquinone is facile.
One such method makes use of hydrogen peroxide as the oxidizer and iodine or an iodine salt as a catalyst for the oxidation occurring in a polar solvent; e.g. isopropyl alcohol.

When heated to near its melting point, 1,4-benzoquinone sublimes, even at atmospheric pressure, allowing for an effective purification.
Impure samples are often dark-colored due to the presence of quinhydrone, a dark green 1:1 charge-transfer complex of quinone with hydroquinone


STRUCTURE AND REDOX:
C–C and C–O bond distances in benzoquinone (Q), its 1e reduced derivative (Q−), and hydroquinone (H2Q).
Benzoquinone is a planar molecule with localized, alternating C=C, C=O, and C–C bonds.
Reduction gives the semiquinone anion C6H4O2−}, which adopts a more delocalized structure.
Further reduction coupled to protonation gives the hydroquinone, wherein the C6 ring is fully delocalized.

REACTIONS AND APPLICATIONS OF PARA-BENZOQUINONE:
Quinone is mainly used as a precursor to hydroquinone, which is used in photography and rubber manufacture as a reducing agent and antioxidant.
Benzoquinonium is a skeletal muscle relaxant, ganglion blocking agent that is made from benzoquinone.

Organic synthesis of p-Benzoquinone:
p-Benzoquinone is used as a hydrogen acceptor and oxidant in organic synthesis.
p-Benzoquinone serves as a dehydrogenation reagent.
p-Benzoquinone is also used as a dienophile in Diels Alder reactions.

Benzoquinone reacts with acetic anhydride and sulfuric acid to give the triacetate of hydroxyquinol.
This reaction is called the Thiele reaction or Thiele–Winter reaction after Johannes Thiele, who first described it in 1898, and after Ernst Winter, who further described its reaction mechanism in 1900.
An application is found in this step of the total synthesis of Metachromin A:

An application of the Thiele reaction, involving a benzoquinone derivative.
Benzoquinone is also used to suppress double-bond migration during olefin metathesis reactions.

An acidic potassium iodide solution reduces a solution of benzoquinone to hydroquinone, which can be reoxidized back to the quinone with a solution of silver nitrate.

Due to its ability to function as an oxidizer, p-Benzoquinone can be found in methods using the Wacker-Tsuji oxidation, wherein a palladium salt catalyzes the conversion of an alkene to a ketone.
This reaction is typically carried out using pressurized oxygen as the oxidizer, but benzoquinone can sometimes preferred.
p-Benzoquinone is also used as a reagent in some variants on Wacker oxidations.

p-Benzoquinone is used in the synthesis of Bromadol and related analogs.

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) is a stronger oxidant and dehydrogenation agent than 1,4-benzoquinone.
Chloranil 1,4-C6Cl4O2 is another potent oxidant and dehydrogenation agent.
Monochloro-p-benzoquinone is yet another but milder oxidant.

METABOLISM OF PARA-BENZOQUINONE:
p-Benzoquinone is a toxic metabolite found in human blood and can be used to track exposure to benzene or mixtures containing benzene and benzene compounds, such as petrol.
The compound can interfere with cellular respiration, and kidney damage has been found in animals receiving severe exposure.
p-Benzoquinone is excreted in its original form and also as variations of its own metabolite, hydroquinone.

Safety:
p-Benzoquinone is able to stain skin dark brown, cause erythema (redness, rashes on skin) and lead on to localized tissue necrosis.
p-Benzoquinone is particularly irritating to the eyes and respiratory system.
Its ability to sublime at commonly encountered temperatures allows for a greater airborne exposure risk than might be expected for a room-temperature solid.

IARC has found insufficient evidence to comment on the compound's carcinogenicity, but has noted that it can easily pass into the bloodstream and that it showed activity in depressing bone marrow production in mice and can inhibit protease enzymes involved in cellular apoptosis.



APPLICATION OF PARA-BENZOQUINONE:
p-Benzoquinone may be used to form benzofuranone derivatives on reacting with anilides of β-aminocrotonic acids via Nenitzescu reaction.
Dienophile employed in Diels-Alder cycloadditions to form naphthoquinones, and 1,4-phenanthrenediones.
Oxidant used in first step of greener amine synthesis from terminal olefins by Wacker oxidation followed by transfer hydrogenation of the resultant imine.

Para-Benzoquinone can be used as A free-radical inhibitor.
Para-Benzoquinone can be used as A catalyst to synthesize highly site-selective N1-alkylated benzotriazoles by N1-alkylation of benzotriazoles with diazo compounds.
Para-Benzoquinone can be used as A hydrogen acceptor and two electron oxidant in Pd-catalyzed Wacker oxidation of aryl olefins aldehydes.
Para-Benzoquinone can be used as A redox mediator in Pd-catalyzed anaerobic electrooxidative homocoupling of aryl-boron derivatives.


Para-Benzoquinone is used as a dienophile in Diels-Alder cycloadditions to prepare naphthoquinones and 1,4-phenanthrenediones.
Para-Benzoquinone acts as a dehydrogenation reagent and an oxidizer in synthetic organic chemistry.
In the Thiele-Winter reaction, it is involved in the preparation of triacetate of hydroxyquinol by reacting with acetic anhydride and sulfuric acid.

Para-Benzoquinone is also used in the synthesis of bromadol and to suppress double- bond migration during olefin metathesis reactions.
Para-Benzoquinone is used as a precursor to hydroquinone which finds application in photography and as a reducing agent and an antioxidant in rubber production.


SAFETY INFORMATION ABOUT PARA-BENZOQUINONE:
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product








CHEMICAL AND PHYSICAL PROPERTIES OF PARA BENZOQUINONE:
Chemical formula C6H4O2
Molar mass 108.096 g•mol−1
Appearance Yellow solid
Odor Acrid, chlorine-like
Density 1.318 g/cm3 at 20 °C
Melting point 115 °C (239 °F; 388 K)
Boiling point Sublimes
Solubility in water 11 g/L (18 °C)
Solubility Slightly soluble in petroleum ether; soluble in acetone; 10% in ethanol, benzene, diethyl ether
Vapor pressure 0.1 mmHg (25 °C)
Magnetic susceptibility (χ) -38.4•10−6 cm3/mol
Density 1.32 g/cm3 (20 °C)
Flash point 77 °C
Ignition temperature 560 °C
Melting Point 112.5 - 113.5 °C
pH value 4 (1 g/l, H₂O, 20 °C)
Vapor pressure 0.12 hPa (20 °C)
Bulk density 700 kg/m3
Solubility 10 g/l
Molecular Weight 108.09 g/mol
XLogP3 0.2
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 0
Exact Mass 108.021129366 g/mol
Monoisotopic Mass 108.021129366 g/mol
Topological Polar Surface Area 34.1Ų
Heavy Atom Count 8
Formal Charge 0
Complexity 149
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
Covalently-Bonded Unit Count 1
Compound Is Canonicalized Yes







SYNONYMS OF PARA BENZOQUINONE:

1,4-Benzochinon [German] [ACD/IUPAC Name]
1,4-Benzoquinone [ACD/IUPAC Name]
1,4-Benzoquinone [French] [ACD/IUPAC Name]
1,4-Dihydrobenzoquinone
1,4-Diossibenzene [Italian]
106-51-4 [RN]
2,5-Cyclohexadiene-1,4-dione [ACD/Index Name]
203-405-2 [EINECS]
773967 [Beilstein]
Benzo-chinon [German]
benzoquinone [Wiki]
cyclohexa-2,5-diene-1,4-dione
Cyclohexadiene-1,4-dione
MFCD00001591 [MDL number]
para-benzoquinone
para-quinone
p-Benzoquinone
p-dioxobenzene
p-quinone
1, 4-Benzoquinone
1,4-Benzoquine
1,4-Benzoquinone|2,5-cyclohexadiene-1,4-dione
1,4-Cyclohexadiene dioxide
1,4-Cyclohexadienedione
1,4-Dioxybenzene
1,4-Dioxy-benzol
1,4-quinone
1,4-苯醌 [Chinese]
19052-63-2 [RN]
2-(2,3-Dihydrobenzob1,4dioxin-6-yl)-4,4,5,5-tetramethyl-1,3,2-diox aborolane
2,5-Cyclohexadien-1-one, 4-carbonyl- [ACD/Index Name]
2,5-cyclohexadiene-1-4-dione
2237-14-1 [RN]
3225-29-4 [RN]
4-Benzochinone [German]
51226-74-5 [RN]
54560-36-0 [RN]
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1,4-benzodioxane
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydrobenzo-1,4-dioxine
benzo-1,4-quinone
CYCLOHEXADIENEDIONE
Eldoquin
p-BQ
p-Chinon [German]
PLQ
p-Quinone, 1,4-Benzoquinone, 1,4-Cyclohexadiene-3,6-dione
Quinone203-405-2MFCD00001591
Steara PBQ
VS-02448
WLN: L6V DVJ
1,4-benzoquinone
2,5-cyclohexadiene-1,4-dione
benzoquinone
NSC-36324
NSC36324
p-benzoquinone
para-benzoquinone
quinone
p-benzoquinone
1,4-BENZOQUINONE
Benzoquinone
Quinone
106-51-4
p-Quinone
cyclohexa-2,5-diene-1,4-dione
para-Benzoquinone
Chinone
2,5-Cyclohexadiene-1,4-dione
para-Quinone
Cyclohexadienedione
1,4-Benzoquine
1,4-Cyclohexadienedione
1,4-Dioxybenzene
Steara pbq
p-Chinon
Benzo-chinon
Benzo-1,4-quinone
1,4-Diossibenzene
Chinon
1,4-Dioxy-benzol
1,4-Cyclohexadiene dioxide
Semiquinone anion
semiquinone radicals
RCRA waste number U197
NCI-C55845
p-Chinon [German]
Benzo-chinon [German]
Caswell No. 719C
USAF P-220
Chinon [Dutch, German]
Cyclohexadiene-1,4-dione
1,4-Benzochinon
NSC 36324
1,4-Dioxy-benzol [German]
CCRIS 933
1,4-Diossibenzene [Italian]
[1,4]benzoquinone
CHEBI:16509
HSDB 1111
Quinone1,4-Benzoquinone
EINECS 203-405-2
MFCD00001591
NSC-36324
UN2587
RCRA waste no. U197
EPA Pesticide Chemical Code 059805
CHEMBL8320
UNII-3T006GV98U
AI3-09068
C6H4O2
DTXSID6020145
3T006GV98U
EC 203-405-2
1,4-Benzoquinone, 99%
DTXCID40145
1,4 benzoquinone
CAS-106-51-4
parabenzochinon
p-Benzoquinona
p-benzo-quinone
1,4-Benzokinon
Quinone; p-BQ
NSC36324
2,4-dione
p-BQ
BZQ (CHRIS Code)
Benzo-1,4-quinone #
QUINONE [MI]
(p-Phenylenedioxy)radical
Lopac-B-1266
QUINONE [WHO-DD]
Benzoquinone [UN2587]
D0M2EM
Epitope ID:116219
WLN: L6V DVJ
Chinon(DUTCH, GERMAN)
cid_4650
PARA-QUINONE [IARC]
Lopac0_000120
SCHEMBL18103
MLS002454445
Benzoquinone, p-; (Quinone)
GTPL6307
2,5-cyclohexadiene-1-4-dione
2,5-Ciclohexadieno-1,4-diona
BDBM22774
1,4-BENZOQUINONE [HSDB]
HMS2230N13
HMS3260G22
AMY21949
Benzoquinone [UN2587] [Poison]
1,4-BENZOQUINONE [USP-RS]
Tox21_202020
Tox21_302970
Tox21_500120
BBL010327
Benzoquinone [UN2587] [Poison]
c0261
LS-403
NA2587
STK398389
AKOS000119965
3,6-Dioxo-1,4-cyclohexadiene-1-ide
CCG-204215
LP00120
SDCCGSBI-0050108.P002
UN 2587
p-Benzoquinone, reagent grade, >=98%
NCGC00015139-01
NCGC00015139-02
NCGC00015139-03
NCGC00015139-04
NCGC00015139-05
NCGC00015139-06
NCGC00015139-07
NCGC00015139-10
NCGC00091053-01
NCGC00091053-02
NCGC00091053-03
NCGC00256505-01
NCGC00259569-01
NCGC00260805-01
SMR000326659
VS-02448
B0089
B0887
EU-0100120
EN300-19699
B 1266
C00472
2,5-Cyclohexadiene-1,4-dione, radical ion(1-)
A801452
Q402719
SR-01000075705
J-503966
SR-01000075705-1
Z104474802
InChI=1/C6H4O2/c7-5-1-2-6(8)4-3-5/h1-4
1,4-Benzoquinone, pharmaceutical secondary standard; traceable to USP
1,4-Benzoquinone, United States Pharmacopeia (USP) Reference Standard
cyclohexa-2,5-diene-1,4-dione; QUINONE RING OF THE PLASTOQUINONE 9
1,4-Benzoquinone, Pharmaceutical Secondary Standard; Certified Reference Material

Para Cresol
cas no: 131-57-7 Benzophenone-3; 4-Methoxy-2-hydroxybenzophenone; (2-hydroxy-4-methoxyphenyl)phenylmethanone; Oxybenzone; Uvinul M-40; Solaquin; 4-Methoxy-2-hydroxybenzophenone butyric acid; 2-Hydroxy-4-methoxybenzophenone;
Para Tertiary Butyl Benzoic Acid
Polyaluminum chlorohydrate; Polyaluminum hydroxychloride CAS NO:1327-41-9
Para Tertiary Butyl Phenol
cas no 57-10-3 n-Hexadecoic acid; Pentadecanecarboxylic acid; n-Hexadecanoic acid; 1-Pentadecanecarboxylic acid; Cetylic acid; Hexadecylic acid;
Para Toluene Sulfonic Acid
PCBTF; 1-(Trifluoromethyl)-4-chlorobenzene; p-Chloro-alpha,alpha,alpha-trifluoro-Toluene; (p-Chlorophenyl) Trifluoromethane; p-(Trifluoromethyl) Chlorobenzene; p-Chloro-alpha,alpha-Trifluorotoluene; ; p-Chlorotrifluoromethylbenzene; p-Trifluoromethylphenyl chloride; 4-Chlorobenzotrifluoride; 1-Chloro-4-(trifluoromethyl)benzene; 4-Chloro-alpha,alpha-trifluorotoluene CAS NO:98-56-6
PARABENS
Parabens are chemicals that are commonly used as preservatives in cosmetic and pharmaceutical products.
Parabens are usually easy to identify by their name, such as methylparaben, propylparaben, butylparaben, or ethylparaben.


INCI Name: Methylparaben Propylparaben Butylparaben
Ingredient origins: Hydrocarbons
Role: Preservative



SYNONYMS:
methyl 4-hydroxybenzoate, propyl 4-hydroxylbenzoate



Parabens are chemicals that are commonly used as preservatives in cosmetic and pharmaceutical products.
Chemically, Parabens are a series of parahydroxybenzoates or esters of parahydroxybenzoic acid (also known as 4-hydroxybenzoic acid).
Research is being conducted to evaluate the potential health implications of Parabens usage.


People can also be exposed to parabens by eating foods and beverages that do not just contain parabens but are also preserved with them.
In the 1970s, propylparaben was designated as “generally recognized as safe” for addition to food up to 0.1 percent.
Parabens are a group of chemicals most commonly used as: preservatives, antimicrobials, flavour enhancers, and fragrance ingredients.


Parabens are a family of ingredients used as preservatives in personal care products.
‘Paraben’ refers to many slightly different paraben forms, some of which can be found in nature.
Parabens are a type of synthetic preservative used to prolong the shelf life of certain ingredients.


By preventing bacteria and mold growth, Parabens allow products to survive for months—even years—in our bathrooms.
(Microorganisms love moisture, so without some sort of preservative, the shampoo sitting for weeks in your humid shower would turn all sorts of funky.)
Parabens are usually easy to identify by their name, such as methylparaben, propylparaben, butylparaben, or ethylparaben.


Other names for these are methyl 4-hydroxybenzoate and propyl 4-hydroxylbenzoate.
Parabens are actually several distinct chemicals with a similar molecular structure.
Several are common in a wide array cosmetic and personal care products: ethylparaben, butylparaben, isobutylparaben, isopropylparaben, methylparaben and propylparaben.


Methylparaben and propylparaben are the most common of these.
Parabens are most common in personal care products that contain significant amounts of water such as shampoos, conditioners, lotions and facial and shower cleansers and scrubs because they discourage the growth of microbes.


While the Cosmetic Ingredient Review recommends concentration limits for single (up to 0.4%) and total paraben concentrations (up to 0.8%) in a single product, these recommendations do not account for exposure to parabens from several products by a single individual.
Parabens are found in nearly all urine samples from U.S. adults regardless of ethnic, socioeconomic or geographic backgrounds.


In one biomonitoring study, adolescents and adult females had higher levels of methylparaben and propylparaben in their urine than did males of similar ages.
Parabens are not water soluble and can penetrate the skin.


As a result, repeated application of a product or multiple products containing parabens could mean almost continuous exposure.
The ubiquity of parabens in personal care products makes this a reasonable scenario.
Parabens enter the body through dermal absorption, ingestion and inhalation, and can enhance the actions of the natural estrogen known as estradiol.


Parabens are a group of compounds widely used as preservatives for their antimicrobial properties.
Parabens are a group of controversial preservatives that include butylparaben, isobutylparaben, propylparaben, methylparaben, and ethylparaben.
All of these were at one time the most widely used group of preservatives used in cosmetics.


Parabens were so popular because of their gentle, non-sensitizing, and highly effective profile in comparison to other preservatives but also because they were derived naturally from plants, a rare phenomenon for a preservative.
Parabens are found in plants in the form of p-hydroxybenzoic acid (PHBA), a chemical that breaks down to become parabens for a plant’s own protection.


Parabens that are manufactured for consumables and personal care products are identical to those found in nature.
The most common types of Parabens are methylparaben, ethylparaben, propylparaben, butylparaben, isopropylparaben and isobutylparaben.



USES and APPLICATIONS of PARABENS:
Parabens are effective preservatives in many types of formulas.
These compounds, and their salts, Parabens are used primarily for their bactericidal and fungicidal properties.
Parabens are found in shampoos, commercial moisturizers, shaving gels, personal lubricants, topical/parenteral pharmaceuticals, sun-tan products, makeup, and toothpaste.


Parabens are also used as food preservatives.
Parabens are additionally found in pharmaceutical products such as topical treatments for wounds.
These treatments help heal wounds by keeping the skin moist and preventing infection.


The antimicrobial properties of parabens play a role in the effectiveness of the treatment.
This application is helpful for those who have chronic wounds and need to prevent infections as much as possible.
Parabens are a group of chemicals that are widely used as preservatives in cosmetics and personal care products such as deodorants, shower gels and body creams.


Parabens are preservatives commonly used in personal care products.
Preservatives are used in to inhibit the growth of microbes or bacteria, making the product safe to use and also extending its shelf lifei.
The three most common parabens in use are methylparaben, propylparaben and butylparaben.


These parabens are known to be eye and skin irritantsii, and have also been linked to breast cancer.
Parabens are not carcinogenic themselves, but they are endocrine disruptors, meaning they have an effect on the normal functioning of hormones within the bodyiii.


Parabens mimic oestrogen within the body, and increased oestrogen is involved with the increase in breast cells, which can also mean the increase in cancerous breast cellsiv.
Parabens are easily absorbed into the skin, being introduced into the system even after just one application.


This is a cause for concern considering Parabens are very often used in products that come into direct contact with the skin such body lotions and deodorants.
We don't use parabens at ecostore but we do still require the use of preservatives to keep our products free of microbes and able to be on the shelf for longer.


Parabens are the most widely used preservative in cosmetics.
Parabens are also used as fragrance ingredients, but consumers won’t find that listed on the label.
Fragrance recipes are considered trade secrets, so manufacturers are not required to disclose fragrance chemicals in the list of ingredients (see also Fragrance/Parfum).


An estimated 75 to 90 per cent of cosmetics contain parabens (typically at very low levels).
Parabens are synthetic chemicals that are used as preservatives in a variety of products, including cosmetics, pharmaceuticals and food.
As preservatives, parabens give products a longer shelf-life and prevent harmful bacteria and mold from growing in the products, according to the U.S. Food and Drug Administration (FDA).


Parabens are a family of related chemicals that are commonly used as preservatives in cosmetic products.
Preservatives may be used in cosmetics to prevent the growth of harmful bacteria and mold, in order to protect both the products and consumers.
Parabens used most commonly in cosmetics are methylparaben, propylparaben, butylparaben, and ethylparaben.


Product ingredient labels typically list more than one paraben in a product, and parabens are often used in combination with other types of preservatives to better protect against a broad range of microorganisms.
Parabens are chemicals that are used as preservatives to ward off substances — fungi, yeast, and bacteria, among others — that shorten the products' shelf life.


You can find Parabens in many of the products that you use every day.
Parabens are preservatives used in a wide variety of personal care products and foods to prevent the growth of microbes.
These endocrine-disrupting chemicals can be absorbed through skin, blood and the digestive system


Parabens are commonly added to cosmetics and other personal care products to prevent the growth of mold, bacteria and yeasts.
Methylparaben and propylparaben are the most commonly used parabens.
Parabens have been widespread in personal care products, foods and beverages since the 1920s.


Manufacturers use parabens to stabilize many personal care and food products and prolong their shelf life.
Without an effective preservative, many products, if used frequently, can get contaminated and become a breeding ground for bacteria, yeast and mold.
Parabens are odorless, tasteless and chemically stable, which makes them ideal for use in food and personal care products.


But safer alternatives are available.
Parabens are a group of preservative ingredients used in cosmetics, personal hygiene products, food products and pharmaceuticals.
Parabens are highly effective in preventing the growth of fungi, bacteria, and yeast that can cause products to spoil, helping to extend shelf life.


Preservatives like parabens may be used in cosmetics to protect against microbial (e.g., bacteria, fungus) growth, both to protect consumers and to maintain product integrity.
In the food industry, parabens have been used for more than 50 years as preservatives and anti-microbial agents.


Some fruits, such as blueberries, contain parabens as a naturally occurring preservative.
Parabens are widely used in confectioneries, cereal-based snacks, dried meats, and much more.
Parabens are chemical preservatives widely used in food and personal care products.


Parabens are a type of endocrine disruptor that may cause serious health harm, especially in the developing body.
If you’re concerned about the impact of parabens on your health, there are ways to avoid them.
Parabens are a group of chemicals that preserve our personal care products.


-blueberries uses of Parabens:
Parabens are derived from para-hydroxybenzoic acid (PHBA) that occurs naturally in many fruits and vegetables, such as cucumbers, cherries, carrots, blueberries and onions.

Parabens also is naturally formed in the human body by the breakdown of some amino acids.
Parabens used in cosmetics are identical to those found in nature, and the human body quickly changes them into natural PHBA and eliminates them.


-cosmetics uses of Parabens:
Parabens (including methylparaben, ethylparaben, propylparaben, butylparaben, isopropylparaben, and isobutylparaben) may be used in products such as makeup, moisturizers, and hair care and shaving products.
Contrary to some reports, most major brands of deodorants and antiperspirants no longer contain parabens.


-Parabens can be ingredients in a number of everyday products, such as:
*drugs
*cosmetics
*pesticides
*natural health products
Some parabens are permitted food additives and can also occur naturally in some foods.



PRODUCTS THAT CONTAIN PARABENS:
-Personal care.
Some products with parabens that you might find in your home are: Shampoo, conditioner, and other hair care products
*Moisturizers and lotions


-Makeup
*Shaving products
In the past, parabens were also used in deodorants and antiperspirants.
Today, many brands have removed parabens as ingredients in their products, but some may still use these chemicals.

Cosmetics and personal care products that are sold in the U.S. are required to list all of their ingredients on the packaging.
This way, you can see if there are parabens or other ingredients or chemicals in them that you want to stay away from.


-Food and drinks.
For the past 50 years, parabens have also been added to foods to stop the growth of microorganisms.
You might find parabens in:
*Cereals
*Candy
*Dried meats
*Beer
*Sauces
*Processed veggies
*Frozen dairy products
*Jams
*Pickles
*Flavored syrups


-Pharmaceuticals
If parabens weren’t added to these foods, they would spoil quicker, and you'd have a higher risk of ingesting food that isn’t safe to eat.
Some foods, like blueberries and barley, have naturally occurring parabens in them.



WHAT KINDS OF PRODUCTS CONTAIN PARABENS?
Parabens are used in a wide variety of cosmetics, as well as in foods and drugs.
Cosmetics that may contain parabens include makeup, moisturizers, hair care products, and shaving products, among others.
Many major brands of deodorants do not currently contain parabens, although some may.



TYPES OF PARABENS:
Parabens have been added to cosmetics and other products since the 1920s.
If you read the ingredients on a bottle of shampoo or foundation, you may see the names of six of the most common ones:
*Methylparaben
*Ethylparaben
*Propylparaben
*Isopropylparaben
*Butylparaben
*Isobutylparaben



PARABENS AT A GLANCE:
*Parabens are a group of chemicals that prevent the growth of mold, bacteria and yeasts.
*Parabens are often added to cosmetics and personal care products to increase shelf-life and stability.



WHERE ARE PARABENS FOUND?
Parabens are most commonly found in cosmetics and personal care items such as lotions, sunscreen, antiperspirants, makeup and hair products.
Parabens may also be found in chewing gum and mouthwash



KEY POINTS/OVERVIEW OF PARABENS:
Parabens are derived from para-hydroxybenzoic acid (PHBA) that occurs naturally in many fruits and vegetables, such as cucumbers, cherries, carrots, blueberries and onions.

Parabens used in cosmetics are identical to those found in nature, and the human body quickly changes them into natural PHBA and eliminates them.
Parabens have been safely used for almost 100 years as preservatives in the food, drug and personal care and cosmetic industries.
Several commonly used parabens have been designated as “Generally Recognized as Safe (GRAS)” for such uses by the FDA since the early 1970s.



TYPES OF PARABENS:
Cosmetics typically contain mixtures of different types of parabens.
The most commonly used six types of Parabens are methyl-, ethyl-, propyl-, isopropyl-, butyl- and isobutylparaben.

The so-called shorter-chain parabens, methyl- and ethyl-, are commonly used in combination, whereas butylparaben is often used alone.
The longer-chain parabens, propyl- and butyl-, are linked to stronger estrogenic activity.
The branched structure has been shown to increase estrogenic activity as well as sensitization potency.



WHAT PRODUCTS CONTAIN PARABENS:
Parabens are used in a wide variety of leave-on and rinse-off products, especially those with a high water content, such as shampoos and conditioners, which people use every day.
Parabens's antimicrobial properties are most effective against fungi and gram positive bacteria.

Moisturizers, face and skin cleaners, sunscreens, deodorants, shaving gels, toothpastes, makeup and many other products contain parabens.
Parabens are absorbed into the body through the skin, metabolized and excreted in urine and bile.

However, daily use of a product or multiple products containing parabens results in direct and continuous exposure, as indicated by nearly ubiquitous detection in biomonitoring surveys.

Personal care products are the greatest contributors to Parabens exposure, as seen in studies comparing paraben levels in the bodies of women, men, adolescents and children who regularly use cosmetics and those who do not.

Adolescent girls who wear makeup every day had 20 times the levels of propylparaben in their urine compared to those who never or rarely wear makeup.
The use of body and face lotions, hair products, sunscreens and makeup have all been predictors of and correlated with remarkably increased levels of urinary parabens.



CHEMISTRY OF PARABENS:
Structure;
Parabens are esters of para-hydroxybenzoic acid, from which the name is derived.
Common parabens include methylparaben (E number E218), ethylparaben (E214), propylparaben (E216), butylparaben and heptylparaben (E209).

Less common parabens include isobutylparaben, isopropylparaben, benzylparaben and their sodium salts.
The general chemical structure of a paraben is shown at the top right of this page, where R symbolizes an alkyl group such as methyl, ethyl, propyl or butyl.



SYNTHESIS OF PARABENS:
All commercially used parabens are synthetically produced, although some are identical to those found in nature.
Parabens are produced by the esterification of para-hydroxybenzoic acid with the appropriate alcohol, such as methanol, ethanol, or n-propanol.
para-Hydroxybenzoic acid is in turn produced industrially from a modification of the Kolbe-Schmitt reaction, using potassium phenoxide and carbon dioxide.



BIOLOGICAL MODE OF ACTION OF PARABENS:
Parabens are active against a broad spectrum of microorganisms.
However, Parabens's antibacterial mode of action is not well understood.

Parabens are thought to act by disrupting membrane transport processes or by inhibiting synthesis of DNA and RNA or of some key enzymes, such as ATPases and phosphotransferases, in some bacterial species.
Propylparaben is considered more active against more bacteria than methylparaben.

The stronger antibacterial action of propylparaben may be due to its greater solubility in the bacterial membrane, which may allow it to reach cytoplasmic targets in greater concentrations.

However, since a majority of the studies on the mechanism of action of parabens suggest that their antibacterial action is linked to the membrane, it is possible that its greater lipid solubility disrupts the lipid bilayer, thereby interfering with bacterial membrane transport processes and perhaps causing the leakage of intracellular constituents.



WHAT PRODUCTS HAVE PARABENS?
Sooo many.
You’ll typically find Parabens in products with a high water content—think shampoos, conditioners, lotions, shaving gels, toothpastes, the list goes on.
Parabens are a hot topic in the beauty world, but they’re also widely used as food preservatives—so much so that scientists have detected them in most grocery store food products.



PHYSICAL and CHEMICAL PROPERTIES of PARABENS:
INCI Name: Methylparaben Propylparaben Butylparaben
Ingredient origins: Hydrocarbons
Role: Preservative
Common name: Parabens



FIRST AID MEASURES of PARABENS:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of PARABENS:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of PARABENS:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of PARABENS:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of PARABENS:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of PARABENS:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available


Parachlorobenzotrifluoride
1,4-Dichlorobenzene; p-Dichlorobenzol; Chloroden; 1,4-Dichloorbenzeen; 1,4-Dichlor-benzol; 1,4-Diclorobenzene; Persia-perazol; Santochlor; Paramoth; Di-Chloricide; Paradi; Paradow; Persia-Perazol; Evola; Parazene; PDCB CAS NO:106-46-7
Para-Dichlorobenzene
PARAFFIN, N° CAS : 8002-74-2; 64742-51-4 - Paraffine, Autres langues : Paraffina, Parafina. Nom INCI : PARAFFIN. N° EINECS/ELINCS : 232-315-6; 265-154-5. Additif alimentaire : E905 Classification : Huile Minérale. La paraffine est une cire solide blanche et tendre constituée de pétrole. Elle est utilisée dans de nombreux domaines comme l'alimentaire et dans la fabrication des bougies. Elle est employée en cosmétique dans les produits de maquillage comme les mascaras ou les rouges à lèvres mais aussi dans de nombreux soins pour le corps. Elle est interdite en bio et est peu biodégradable.Ses fonctions (INCI) Agent d'entretien de la peau : Maintient la peau en bon état Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques Agent parfumant : Utilisé pour le parfum et les matières premières aromatiques
PARAFFIN WAX
Paraffin wax is a soft colorless solid derived from petroleum, coal, or oil shale that consists of a mixture of hydrocarbon molecules containing between 20 and 40 carbon atoms.
Paraffin wax is solid at room temperature and begins to melt above approximately 37 °C (99 °F), and its boiling point is above 370 °C (698 °F).
Common applications for paraffin wax include lubrication, electrical insulation,and candles;dyed paraffin wax can be made into crayons.

CAS: 8002-74-2
MF: C21H27NO3
MW: 341.44398
EINECS: 232-315-6

Synonyms
PARAFFIN IN PASTILLE FORM 51-53 PH EUR,B;PARAFFIN IN PASTILLE FORM 52-54 PH EUR,B;PARAFFIN IN BLOCK FORM 42-44 25 KG;PARAFFIN IN BLOCK FORM 46-48 1 KG;PARAFFIN IN PASTILLE FORM 56-58 PH EUR,B;PARAFFIN IN PASTILLE FORM 57-60 PH EUR,B;PARAFFIN IN BLOCK FORM 46-48 25 KG;PARAFFIN IN BLOCK FORM 42-44 1 KG

Paraffin wax is not to be confused with kerosene and other petroleum products that are sometimes called paraffin.
Un-dyed, unscented paraffin candles are odorless and bluish-white.
Paraffin wax was first created by Carl Reichenbach in Germany in 1830 and marked a major advancement in candlemaking technology, as it burned more cleanly and reliably than tallow candles and was cheaper to produce.
In chemistry, paraffin is used synonymously with alkane, indicating hydrocarbons with the general formula CnH2n+2.
The name is derived from Latin parum ("very little") + affinis, meaning "lacking affinity" or "lacking reactivity", referring to paraffin's unreactive nature.
Paraffin wax is mostly found as a white, odorless, tasteless, waxy solid, with a typical melting point between about 46 and 68°C (115 and 154°F) and a density of approximately 900, is insoluble in water, but soluble in ether, benzene, and certain esters.

Paraffin wax is often classed as a stable chemical since it is unaffected by most common chemical reagents but burns readily.
Paraffin wax is the common name for the mixture of solid higher alkanes, the molecular formula is CnH2n+2, where n=20-40.
The excess oil residue in the wax is removed through the process of petroleum refining.
Paraffin wax is then deoiled and separated by vacuum distillation.
The main component of refined paraffin is saturated normal alkanes with carbon number of about 20-40, containing a small amount of isomers and alkanes.
Paraffin wax, also commonly called ‘paraffin’, is a colourless or white, tasteless, odourless, translucent waxy solid.

Paraffin wax has a typical melting point between about 46°C and 68°C.
Pure paraffin wax is a combustible substance and insoluble in water but soluble in petroleum solvents and stable under normal conditions of use.
Paraffin wax has been identified as an excellent electrical insulator.
Paraffin wax is also used in the manufacturing of paraffin papers, candles, food packaging materials, varnishes, floor polishes, to extract perfumes from flowers, in lubricants, and cosmetics.
Paraffin wax is also used in water-proofing wood, and cork.
White translucent tasteless odorless solids.
Density 0.88- 0.92 g / cm3.
Insoluble in water.
Melting range 47-65°C.
Used in candles, lubricants, crayons, floor polishes, cosmetics, chewing gum.

Paraffin wax Chemical Properties
Melting point: 58-62 °C ((ASTM D 87))
Boiling point: 322 °C
Density: 0.82 g/mL at 20 °C
Refractive index: n20/D 1.45
FEMA: 3216 | PARAFFIN WAX
Fp: 113 °C
Storage temp.: Store below +30°C.
Solubility: Soluble in chloroform, ether, volatile oils, and most warm fixed oils; slightly Soluble in ethanol; practically insoluble in acetone, ethanol (95%), and water.
Paraffin can be mixed with most waxes if melted and cooled.
Form: extra-low viscosity oil
Color: white
Odor: odorless
Odor Type: odorless
explosive limit: 0.6-6.5%(V)
Dielectric constant: 2.1-2.5(0.0℃)
CAS DataBase Reference: 8002-74-2
EPA Substance Registry System: Paraffin waxes and Hydrocarbon waxes (8002-74-2)

Paraffin wax, also known as crystalline wax, is usually a white, odorless waxy solid.
Paraffin wax melts at 47°C-64°C and has a density of about 0.9g/cm3.
Paraffin wax is soluble in gasoline, carbon disulfide, xylene, ether, benzene, chloroform, and tetrachloride.
Non-polar solvents such as carbon, naphtha, etc., are insoluble in polar solvents such as water and methanol.
Paraffin wax is a good insulator, its resistivity is 1013-1017 ohm·m, which is higher than most materials except some plastics (especially Teflon).
Fully refined paraffin waxes are a hard, white crystalline material derived from petroleum.
Paraffin waxes are predominately composed of normal, straight-chain hydrocarbons.

The water-repellent and thermoplastic properties of paraffin waxes make them ideal for many applications.
Typical end uses include cereal, delicatessen, and household wrap, corrugated containers, candles, cheese and vegetable coatings, and hot melt adhesives.
Paraffin wax is colorless or white with an odorless mass.
Paraffin wax consists of a mixture of solid aliphatic hydrocarbons.
Paraffin wax is used in the manufacture of paraffin papers, candles, food packaging materials, varnishes, floor polishes, to extract perfumes from flowers, in lubricants, and cosmetics.
Paraffin wax is also used in waterproofing wood and cork.

Paraffin wax is mostly found as a white, odorless, tasteless, waxy solid, with a typical melting point between about 46 and 68 °C (115 and 154 °F), and a density of around 900 kg/m3.
Paraffin wax is insoluble in water, but soluble in ether, benzene, and certain esters.
Paraffin is unaffected by most common chemical reagents but burns readily.
Paraffin wax's heat of combustion is 42 MJ/kg.
Paraffin wax is an excellent electrical insulator, with a resistivity of between 1013 and 1017 ohm-metre.
This is better than nearly all other materials except some plastics (notably PTFE).
Paraffin wax is an effective neutron moderator and was used in James Chadwick's 1932 experiments to identify the neutron.

Paraffin wax is an excellent material for storing heat, with a specific heat capacity of 2.14–2.9 J⋅g−1⋅K−1 (joules per gram per kelvin) and a heat of fusion of 200–220 J⋅g−1.
Paraffin wax phase-change cooling coupled with retractable radiators was used to cool the electronics of the Lunar Roving Vehicle during the crewed missions to the Moon in the early 1970s.
Wax expands considerably when Paraffin wax melts and so is used in wax element thermostats for industrial, domestic and, particularly, automobile purposes.
If pure paraffin wax melted to the approximate flash point in a half open glass vessel which is then suddenly cooled down, then its vapors may autoignite as result of reaching boiling liquid pressure.

Composition
Paraffin wax is a mixture of solid higher alkanes, the molecular formula of the main component is CnH2n+2, where n=17~35.
The main components are straight-chain alkanes, a small amount of alkane with individual branches and monocyclic cycloalkanes with long side chains; straight-chain alkanes are mainly n-docosane (C22H46) and n-octadecane (C28H58).

History
Paraffin wax was first created in 1830 by German chemist Karl von Reichenbach when he attempted to develop a method to efficiently separate and refine waxy substances naturally occurring in petroleum.
Paraffin represented a major advance in the candle-making industry because it burned cleanly and was cheaper to manufacture than other candle fuels such as beeswax and tallow.
Paraffin wax initially suffered from a low melting point.
Paraffin wax was remedied by adding stearic acid.
The production of paraffin wax enjoyed a boom in the early 20th century due to the growth of the oil and meatpacking industries, which created paraffin and stearic acid as byproducts.

Wax
Paraffin wax is of two general types: (i) paraffin wax in petroleum distillates and (ii) microcrystalline wax in petroleum residua.
Paraffin wax is a solid crystalline mixture of straightchain (normal) hydrocarbons ranging from 20 to 30 carbon atoms per molecule, and even higher.
Paraffin wax is a solid crystalline mixture of straightchain (normal) hydrocarbons ranging from C20 to C30 and possibly higher, that is, CH3(CH2)nCH3 , where n≥18.
Paraffin wax is distinguished by its solid state at ordinary temperatures (25°C, 77°F) and low viscosity (35–45 SUS at 99°C, 210°F) when melted.
However, in contrast to petroleum wax, petrolatum (petroleum jelly), although solid at ordinary temperatures, does in fact contain both solid and liquid hydrocarbons.
Paraffin wax is essentially a low-melting, ductile, microcrystalline wax.
Microcrystalline waxes form approximately 1–2% w/w of crude oil and are valuable products having numerous applications.
These waxes are usually obtained from heavy lube distillates by solvent dewaxing and from tank bottom sludge by acid clay treatment.
However, these crude wax products usually contain appreciable quantity (10–20% w/w) of residual oil and, as such, are not suitable for many applications such as paper coating, electrical insulation, textile printing, and polishes.

Microcrystalline waxes
Microcrystalline waxes are a type of wax produced by de-oiling petrolatum, as part of the petroleum refining process.
In contrast to the more familiar paraffin wax, which contains mostly unbranched alkanes, microcrystalline wax contains a higher percentage of iso-paraffin (branched) and naphthene hydrocarbons.
Paraffin wax is characterized by the fineness of its crystals in contrast to the larger crystal of paraffin wax.
Paraffin wax consists of high-molecular-weight saturated aliphatic hydrocarbons.
Paraffin wax is generally darker, more viscous, denser, tackier, and more elastic than paraffin waxes, and has a higher molecular weight and melting point.

The elastic and adhesive characteristics of microcrystalline waxes are related to the non-straightchain components that they contain.
Typical microcrystalline wax crystal structure is small and thin, making them more flexible than paraffin wax.
Microcrystalline waxes when produced by wax refiners are typically produced to meet a number of ASTM specifications, which include congealing point (ASTM D938), needle penetration (D1321), color (ASTM D6045), and viscosity (ASTM D445).
Microcrystalline wax is also a key component in the manufacture of petrolatum.
The branched structure of the carbon chain backbone allows oil molecules to be incorporated into the crystal lattice structure.
The desired properties of the petrolatum can be modified by using microcrystalline wax bases of different congeal points (ASTM D938) and needle penetration (ASTM D1321).

Uses
Paraffin wax, or hard wax, is a mixture of solid hydrocarbons, mainly alkanes.
Paraffinwax can be added to medicinal agents.
Petroleumwax and petrolatum are the only hydrocarbons permitted for use in food products.
Paraffin wax is used as a household wax and extensively as a coating for food containers and wrappers.
Paraffin Wax is used to embed tissues to be used in research.
Paraffin wax can be used as a phase changing material in a wide range of applications which include solar based water heaters, microcapsules and thermal energy devices (TEDs).
Used in the production of candles, crayons, wax paper, rubber, wires, cables, plates, waterproof materials, electrical insulation, food packaging, precision casting, general telecommunications equipment, textiles, printing, metal rust prevention, and other chemicals required by various industrial sectors raw material.

Paraffin wax can also be used for oxidation to generate synthetic fatty acids.
Paraffin wax can also be made into detergents, emulsifiers, dispersants, plasticizers, greases, etc.
As a kind of latent heat storage material, paraffin wax has the advantages of large latent heat of phase change, small volume change during solid-liquid phase change, good thermal stability, no supercooling phenomenon, and low price.
Paraffin wax is used in aviation, aerospace, microelectronics, etc. Various fields such as scientific and technological systems and house energy saving have been widely used.

1. Paraffin wax can be made into flake or needle crystals obtained by solvent dewaxing or freezing crystallization of wax, pressing dewaxing to obtain wax paste, and then solvent deoiling and refining.
Used to make higher fatty acids, higher alcohols, matches, candles, waterproofing agents, ointments, electrical insulating materials, etc.
2. Paraffin wax is divided into food grade (food grade and packaging grade, the former is excellent) and industrial grade.
Food grade is non-toxic and industrial grade is not edible.
3. Because of its high oil content, crude paraffin is mainly used to make matches, fiberboards, tarpaulins, etc.
After adding polyolefin additives to paraffin wax, its melting point increases, adhesion and flexibility increase, and Paraffin wax is widely used in moisture-proof and waterproof packaging paper, cardboard, surface coating of certain textiles and candle production.

4. After immersing the paper in paraffin wax, various wax papers with good waterproof performance can be prepared, which can be used in food, medicine and other packaging, metal rust prevention and printing industries; after paraffin wax is added to cotton yarn, the textiles can be soft, smooth and smooth.
Paraffin wax is elastic; paraffin wax can also be used to make detergents, emulsifiers, dispersants, plasticizers, greases, etc.
5. Fully refined paraffin and semi-refined paraffin have a wide range of uses.
They are mainly used as components and packaging materials for food, oral medicines and certain commodities (such as wax paper, crayons, candles, carbon paper), coating materials for baking containers, and Fruit preservation, insulation of electrical components, improvement of rubber aging resistance and flexibility, etc.

Pharmaceutical Applications
Paraffin wax is mainly used in topical pharmaceutical formulations as a component of creams and ointments.
In ointments, Paraffin wax may be used to increase the melting point of a formulation or to add stiffness.
Paraffin wax is additionally used as a coating agent for capsules and tablets, and is used in some food applications.
Paraffin wax coatings can also be used to affect the release of drug from ion-exchange resin beads.

Reactivity Profile
Paraffin wax, may be incompatible with strong oxidizing agents.
Charring may occur followed by ignition of unreacted portion and other nearby combustibles.
In other settings, mostly unreactive.
Not affected by aqueous solutions of acids, alkalis, most oxidizing agents, and most reducing agents.
When heated sufficiently or when ignited in the presence of air, oxygen or strong oxidizing agents, they burn exothermically.

Health Hazard
Exposures to paraffi n for a prolonged period cause several types of skin disorders, The adverse health effects to skin include chronic dermatitis, wax boils, folliculitis, comedones, papules, melanoderma, and hyperkeratoses.
Studies of Hendricks et al. indicated the development of carcinoma of the scrotum in workers exposed to crude petroleum wax.
Carcinoma of the scrotum in occupational workers began with a normal hyperkeratotic nevus-like lesion, which subsequently resulted in a squamous cell carcinoma.

Manufacturing
The feedstock for paraffin is slack wax, which is a mixture of oil and wax, a byproduct from the refining of lubricating oil.
The first step in making paraffin wax is to remove the oil (de-oiling or de-waxing) from the slack wax.
The oil is separated by crystallization.
Most commonly, the slack wax is heated, mixed with one or more solvents such as a ketone and then cooled.
As Paraffin wax cools, wax crystallizes out of the solution, leaving only oil.
This mixture is filtered into two streams: solid (wax plus some solvent) and liquid (oil and solvent).

After the solvent is recovered by distillation, the resulting products are called "product wax" (or "press wax") and "foots oil".
The lower the percentage of oil in the wax, the more refined Paraffin wax is considered (semi-refined versus fully refined).
The product wax may be further processed to remove colors and odors.
The wax may finally be blended together to give certain desired properties such as melt point and penetration.
Paraffin wax is sold in either liquid or solid form.
PARAFFIN WAX
DESCRIPTION:
Paraffin wax (or petroleum wax) is a soft colorless solid derived from petroleum, coal, or oil shale that consists of a mixture of hydrocarbon molecules containing between 20 and 40 carbon atoms.
Paraffin wax is solid at room temperature and begins to melt above approximately 37 °C (99 °F), and its boiling point is above 370 °C (698 °F).
Common applications for paraffin wax include lubrication, electrical insulation, and candles; dyed paraffin wax can be made into crayons.

CAS Number: 8002-74-2



Paraffin wax is distinct from kerosene and other petroleum products that are sometimes called paraffin.

Un-dyed, unscented paraffin candles are odorless and bluish-white.
Paraffin wax was first created by Carl Reichenbach in Germany in 1830 and marked a major advancement in candlemaking technology, as it burned more cleanly and reliably than tallow candles and was cheaper to produce.

In chemistry, paraffin is used synonymously with alkane, indicating hydrocarbons with the general formula CnH2n+2.
The name is derived from Latin parum ("very little") + affinis, meaning "lacking affinity" or "lacking reactivity", referring to paraffin's unreactive nature.

Paraffin wax is a white or colorless soft, solid wax.
Paraffin wax is made from saturated hydrocarbons.

Paraffin wax is often used in skin-softening salon and spa treatments on the hands, cuticles, and feet because it’s colorless, tasteless, and odorless.
Paraffin wax can also be used to provide pain relief to sore joints and muscles.

Paraffin wax has many other uses, too.
Paraffin wax is often used as lubrication, electrical insulation, and to make candles and crayons


Paraffin wax is a by-product of heating or distilling petroleum, also known as crude oil.
Paraffin wax is a solid waxy substance that companies often use to make candles.
Paraffin wax also has other uses, such as a stiffening agent in ointments or an anti-inflammatory cream for the skin.

People often use it to relieve the symptoms of arthritis, and some spas use Paraffin wax as a therapeutic treatment.
Paraffin wax is also a mineral oil and an ingredient in many skin creams, lotions, and gels.

Paraffin waxes are produced as by-products of base oil production process in petroleum refineries.
This by-product is refined in paraffin production facilities to get semi or fully refined grades.
Rafination generally consist s of deoiling, bleaching and deodorization.

Paraffinic products can be divided into two genaral categories: Paraffin waxes and microcrystalline waxes.
Paraffin waxes also called macrocrystalline waxes consist of macrocrystals which are arranged in a more regular pattern and contains high percentage of unbranched molecules.
Paraffin waxes are higher grade alkanes which are very hydrophobic and chemically inert.

Application areas include hot melt adhesives, PVC production, textile industry, explosives,candlemaking, paper and packaging, inks, paints, match production, rodent bait carrier, fishnet protection, tire and rubber industry.

Paraffin Wax is a by-product of the petro-chemical industry.
Paraffin Wax has a low melting point of 50-60°c and a brittle texture, making Paraffin Wax unsuitable for encaustic painting or as an additive to oil paints, but it can be used to impart softness to lithographic crayons.
As a petroleum product, Paraffin Wax is more inert than animal or vegetable waxes, and is therefore not saponified (turned into soap) by alkali substances.


PRODUCTION OF PARAFFIN WAX:
Paraffin wax from a solvent dewaxing operation is commonly known as slack was, and the processes employed for the production of waxes arc aimed at de-oiling the slack wax (petroleum wax concentrate).

Was "waling was originally used to separate wax fractions with various melting points from the wax obtained from shale oils.
Wax sweating is Still used to some extent but is being replaced by the more convenient crystallization process.
In wax sweating, a cake of slack wax is slowly warmed to a temperature at which the oil in the wax and the lower-melting waxes become fluid and drip (or sweat) from the bottom of the cake. leaving a residue of higher-melting wax.

Sweated waxes generally contain small amounts of unsaturated aromatic and sulfur compounds, which are the source of unwanted color, odor, and the aisle that reduce the ability of the wax to resist oxidation; the commonly used method of removing these impurities is clay treatment of the molten wax.

Wax crystallization, like wax sweating, separates slack wax into Inactions. but instead of using the differences in melting points, it makes use of the different solubility of the wax fractions in a solvent. such as the ketone used in the dewaxing process.
When a mixture of ketone and slack wax is heated, the slack wax usually dissolves completely. and it' the solution is cooled slowly, a temperature is reached at which a crop of wax crystals is formed.
These crystals will all be of the same melting point. and if they arc removed by filtration, a wax fraction with a specific melting point is obtained.
If the clear filtrate is further cooled, the second crop of wax crystals with a lower melting point is obtained.
Thus, by alternate cooling and filtration, the slack wax can be subdivided into a large number of wax fractions, each with different melting points.

Chemically. paraffin wax is a mixture of saturated aliphatic hydrocarbons (with the general formula.
Wax is the residue extracted when dewaxing lubricant oils and they have a crystalline structure with canton number greater than 12.
The main characteristics of wax are (i) colorless. (ii) Odorless. (iii) translucent, and (iv) a melting point above 45°C (113°F).


PROPERTIES OF PARAFFIN WAX:
Paraffin wax is mostly found as a white, odorless, tasteless, waxy solid, with a typical melting point between about 46 and 68 °C (115 and 154 °F), and a density of around 900 kg/m3.
Paraffin wax is insoluble in water, but soluble in ether, benzene, and certain esters.
Paraffin is unaffected by most common chemical reagents but burns readily.
Its heat of combustion is 42 MJ/kg.


The hydrocarbon C31H64 is a typical component of paraffin wax.
Paraffin wax is an excellent electrical insulator, with a resistivity of between 1013 and 1017 ohm metre.
This is better than nearly all other materials except some plastics (notably Teflon).
It is an effective neutron moderator and was used in James Chadwick's 1932 experiments to identify the neutron.

Paraffin wax is an excellent material for storing heat, with a specific heat capacity of 2.14–2.9 J g−1 K−1 (joules per gram kelvin) and a heat of fusion of 200–220 J g−1.
Paraffin wax phase-change cooling coupled with retractable radiators was used to cool the electronics of the Lunar Roving Vehicle during the crewed missions to the Moon in the early 1970s.
Wax expands considerably when it melts and this allows its use in wax element thermostats for industrial, domestic and, particularly, automobile purposes.

If pure parraffine wax melted to the approximate flash point in a half open glass vessel which is then suddenly cooled down its vapors may autoignite as result of reaching boiling liquid pressure.


Petroleum wax is of two general types: the paraffin waxes in petroleum distillates and the microcrystalline waxes in petroleum residua.
The melting point of the wax is not directly related to its boiling point because waxes contain hydrocarbons of different chemical nature.
Nevertheless, waxes are graded according to their melting point (ASTM 1)87, IP 55) and oil content (ASTM D721. IP In).


The melting point of paraffin was (ASTM D87. IP 55) has both direct and indirect significance in most wax utilization.
All wax grades are commercially indicated in a range of melting temperatures rather than at a single value, and a range of I °C (2°F) usually indicates a good degree of refinement.
Other common physical properties that help to illustrate the degree of refinement of the wax are color (ASTM D156), oil content (ASTM D721, IP 158), and viscosity (ASTM D88, ASTM D445, IP 71).

Fully refined paraffin waxes are a hard, white crystalline material derived from petroleum.
Paraffin waxes are predominately composed of normal, straight-chain hydrocarbons.

The water-repellent and thermoplastic properties of paraffin waxes make them ideal for many applications.
Typical end uses include cereal, delicatessen, and household wrap, corrugated containers, candles, cheese and vegetable coatings, and hot melt adhesives.

Paraffin wax is mostly found as a white, odorless, tasteless, waxy solid, with a typical melting point between about 46 and 68°C (115 and 154°F) and a density of approximately 900, is insoluble in water, but soluble in ether, benzene, and certain esters.
Paraffin wax is often classed as a stable chemical since it is unaffected by most common chemical reagents but burns readily.

Microcrystalline waxes are a type of wax produced by de-oiling petrolatum, as part of the petroleum refining process.
In contrast to the more familiar paraffin wax, which contains mostly unbranched alkanes, microcrystalline wax contains a higher percentage of iso-paraffin (branched) and naphthene hydrocarbons.
It is characterized by the fineness of its crystals in contrast to the larger crystal of paraffin wax.

It consists of high-molecular-weight saturated aliphatic hydrocarbons.
It is generally darker, more viscous, denser, tackier, and more elastic than paraffin waxes, and has a higher molecular weight and melting point.

The elastic and adhesive characteristics of microcrystalline waxes are related to the non-straight-chain components that they contain.
The typical microcrystalline wax crystal structure is small and thin, making them more flexible than paraffin wax.





Color:
Paraffin wax is generally white in color, whereas microcrystalline wax and petrolatum range from white to almost black.
A fully refined wax should be virtually colorless (water-white) when examined in the molten state.
The absence of color is of particular importance in wax used for pharmaceutical purposes or for the manufacture of food wrappings.

The significance of the color of microcrystalline wax and petrolatum depends on the use for which they are intended.
In some applications (e.g., the manufacture of corrosion preventives), color may be of little importance.

The Saybolt color test method (ASTM D156) is used for nearly colorless waxes, and in this method, a melted sample is placed in a heated vertical tube mounted alongside a second tube containing standard color disks.
An optical viewer allows simultaneous viewing of both tubes.
The level of the sample is decreased until its color is lighter than that of the standard, and the color number above this level is the Saybolt color.

The test method for the color of petroleum products (ASTM DI500, IP 196) is for wax and petrolatum that are too dark for the Saybolt colorimeter.
A liquid sample is placed in the test container, a glass cylinder of 30-35 min ID, and compared with colored glass disks ranging in value from 0-5 to 8-0, using a standard light source.
If an exact match is not found, and the sample color falls between two standard colors, the higher of the two colors is reported.

The Lovibond Tintometer (IP 17) is used to measure the tint and depth of color by comparison with a series of red, yellow, and blue standard glasses.
Waxes and petrolatum are tested in the molten state, and a wide range of cell sizes is available for different types.














HISTORY OF PARAFFIN WAX:
Paraffin wax was first created in 1830 by German chemist Karl von Reichenbach when he attempted to develop a method to efficiently separate and refine waxy substances naturally occurring in petroleum.
Paraffin represented a major advance in the candlemaking industry, because it burned cleanly and was cheaper to manufacture than other candle fuels.
Paraffin wax initially suffered from a low melting point.

This was remedied by adding stearic acid.
The production of paraffin wax enjoyed a boom in the early 20th century due to the growth of the oil and meatpacking industries, which created paraffin and stearic acid as byproducts.


Paraffin wax is acquired from petroleum by dewaxing light lubricating oil stocks.
It was first produced in 1830 by Carl Reichenbach in Germany and commemorated a key advancement in candle making technology, as its burn was cleaner, more consistent than tallow candles and was cheaper to produce.

Initially, paraffin wax had a low melting point, however, the addition of stearic acid later solved this.
Paraffin wax production was thriving in the early 20th century from a rise in meatpacking and oil industries which generated paraffin and stearic acid as by-products.




HOW IS PARAFFIN WAX MADE?:
Paraffin feedstock is slack wax, a combination of oil and wax and a by-product from the refining of lubricating oil.
Firstly, the oil is removed (de-oiled or de-waxed) from the slack wax and separated by crystallisation.
Generally, the slack wax is heated, mixed with a solvent such as ketone and then cooled.

The wax then crystalises out of the solution and the oil remains before the mixture is then filtered into two streams:
• Solid – wax plus some solvent
• Liquid – oil and solvent
Once the solvent is retrieved by distillation, the subsequent products are “product wax” (or “press wax”) and “foots oil”.
The lower percentage of oil in the wax, the more refined it is (semi-refined vs fully-refined).

The product wax may be processed more to remove any colours and odours.
The wax may then be blended to achieve specific required products such as penetration and melt point.
The paraffin wax is then supplied in either liquid or solid form.


MANUFACTURING OF PARAFFIN WAX:
The feedstock for paraffin is slack wax, which is a mixture of oil and wax, a byproduct from the refining of lubricating oil.
The first step in making paraffin wax is to remove the oil (de-oiling or de-waxing) from the slack wax.
The oil is separated by crystallization.

Most commonly, the slack wax is heated, mixed with one or more solvents such as a ketone and then cooled.
As it cools, wax crystallizes out of the solution, leaving only oil.
This mixture is filtered into two streams: solid (wax plus some solvent) and liquid (oil and solvent).

After the solvent is recovered by distillation, the resulting products are called "product wax" (or "press wax") and "foots oil".
The lower the percentage of oil in the wax, the more refined it is considered (semi-refined versus fully refined).
The product wax may be further processed to remove colors and odors.

The wax may finally be blended together to give certain desired properties such as melt point and penetration.
Paraffin wax is sold in either liquid or solid form.

APPLICATIONS OF PARAFFIN WAX:
In industrial applications, it is often useful to modify the crystal properties of the paraffin wax, typically by adding branching to the existing carbon backbone chain.
The modification is usually done with additives, such as EVA copolymers, microcrystalline wax, or forms of polyethylene.
The branched properties result in a modified paraffin with a higher viscosity, smaller crystalline structure, and modified functional properties.

Pure paraffin wax is rarely used for carving original models for casting metal and other materials in the lost wax process, as it is relatively brittle at room temperature and presents the risks of chipping and breakage when worked.
Soft and pliable waxes, like beeswax, may be preferred for such sculpture, but "investment casting waxes," often paraffin-based, are expressly formulated for the purpose.

In a histology or pathology laboratory, paraffin wax is used to impregnate tissue prior to sectioning thin samples.
Water is removed from the tissue through ascending strengths of alcohol (75% to absolute), and the tissue is cleared in an organic solvent such as xylene.
The tissue is then placed in paraffin wax for several hours, then set in a mold with wax to cool and solidify.
Sections are then cut on a microtome.



Paraffin has a variety of practical uses in industries that range from medicine and agriculture to cosmetics.
While the very first usage of paraffin dates back to the 19th century as paraffin wax in candles, the oil has since found use in many other forms.
Paraffin is commonly used as a fuel for jet engines and rockets, as well as a fuel or fuel component for diesel and tractor engines.

Common paraffin uses include:
Paraffin wax: a white or colourless soft solid used as a lubricant, candles, crayons, electrical insulation and petroleum jelly
Liquid paraffin (drug): a very highly refined mineral oil used in cosmetics and medicines

Alkane: a saturated hydrocarbon used as a chemical solvent and in plastics
Kerosene: a fuel also known as paraffin
Mineral oil: any of various colourless, odourless, light mixtures of alkanes in the C15 – C40 range from non-vegetable (mineral) source, particularly a distillate of petroleum

Petroleum jelly (soft paraffin)
Tractor vaporising oil: a fuel for petrol-paraffin engines
Paraffin fuel: for prama-stoves or paraffin stoves, used in households in rural parts of South Africa
Liquid paraffin is a mineral oil that comes in two forms: either heavy liquid paraffin oil or light liquid paraffin oil.

The terms kerosene and paraffin overlap where the latter is used as a liquid fuel.
Whereas paraffin wax is a waxy solid, liquid paraffin is more viscous and highly refined and can be used as a laxative.

Other uses of paraffin include:
• A coolant for electrical systems
• A hydraulic fluid











OTHER USES OF PARAFFIN WAX:
• Candle-making
• Wax carving
• Bicycle chain lubrication
• Coatings for waxed paper or waxed cotton
• Food-grade paraffin wax:
• Shiny coating used in candy-making; although edible, it is nondigestible, passing through the body without being broken down
• Coating for many kinds of hard cheese, like Edam cheese
• Sealant for jars, cans, and bottles
• Chewing gum additive
• Investment casting
• Anti-caking agent, moisture repellent, and dustbinding coatings for fertilizers
• Agent for preparation of specimens for histology
• Bullet lubricant – with other ingredients, such as olive oil and beeswax
• Phlegmatizing agent, commonly used to stabilise/desensitize high explosives such as RDX
• Crayons
• Solid propellant for hybrid rocket motors
• Component of surfboard wax, ski wax, and skateboard wax
• Ink. Used as the basis for solid ink different color blocks of wax for thermal printers. The wax is melted and then sprayed on the paper producing images with a shiny surface
• Microwax: food additive, a glazing agent with E number E905
• Forensic investigations: the nitrate test uses paraffin wax to detect nitrates and nitrites on the hand of a shooting suspect
• Antiozonant agents: blends of paraffin and micro waxes are used in rubber compounds to prevent cracking of the rubber; the admixture of wax migrates to the surface of the product and forms a protective layer. The layer can also act as a release agent, helping the product separate from its mould.[26]
• Mechanical thermostats and actuators, as an expansion medium for activating such devices
• As a potting material to encapsulate electronic components such as guitar pickups, transformers, and inductors, to prevent moisture ingress and to reduce electromagnetically-induced acoustic noise and microphonic effects
• Textile manufacturing processes, such as that used for Eisengarn thread.
• Thickening agent in many paintballs
• Moisturiser in toiletries and cosmetics such as Vaseline.
• Prevents oxidation on the surface of polished steel and iron
• Phase change material for thermal energy storage
• Used by MESSENGER (Mercury spacecraft), when the spacecraft was unable to radiate excessive heat.
• Manufacture of boiled leather armor and books
• Neutron radiation shielding
• Wax baths for occupational and physical therapies and cosmetic treatments
• Paraffin is effective in the treatment of Osteoporosis of the hand joints. Treatment consists of dip-wrapped paraffin bath therapy for 15 minutes until paraffin cooled for five days a weeks. The use of paraffin wax bath has been shown to decrease pain at rest and during ADLs compared to groups who did not receive wax therapy.
• Improvements in grip strength and pinch strength have been found in patients with Carpel Tunnel Syndrome, Osteoarthritis, spasticity, and post-traumatic stiffness for those who have used paraffin bath therapy along with traditional physical therapy in their recovery. It has been found that patients who have used paraffin bath therapy have yielded lower VAS and AUSCAN scores (pain scores) compared to those who did not.
• Used for wood finishing
• Used as a fuel for fire breathing
• Used in Lava Lamps

BENEFITS OF PARAFFIN WAX:
Cosmetic benefits:
Cosmetically, paraffin wax is often applied to the hands and feet.
The wax is a natural emollient, helping make skin supple and soft.
When applied to the skin, it adds moisture and continues to boost the moisture levels of the skin after the treatment is complete.

It can also help open pores and remove dead skin cells.
That may help make the skin look fresher and feel smoother.

Therapeutic benefits:
Paraffin wax may be used to help relieve pain in the hands of people with:
• Osteoarthritis
• rheumatoid arthritis
• fibromyalgia
• other joint mobility issues

Paraffin wax acts like a form of heat therapy and can help increase blood flow, relax muscles, and decrease joint stiffness.
Paraffin wax can also minimize muscle spasms and inflammation as well as treat sprains.


Paraffin wax has some potential therapeutic uses.
Some salons and spas use it as a skin-softening treatment or pain relief for sore joints and muscles.
The two main benefits of paraffin wax are its moisturizing or skin-softening properties and its use in heat therapy.

Moisturizing:
Spas and salons often use paraffin wax in skin-softening treatments to moisturize the hands, feet, and cuticles.
Paraffin is an occlusive moisturizerTrusted Source, which means it forms a physical barrier on the skin to prevent water loss.
This can make a person’s skin feel supple and soft.

Occlusive agents such as paraffin wax can also help relieve symptoms of dry skin conditions such as atopic dermatitis.
However, occlusive moisturizers may cause the skin to feel greasy.
The thick barrier on the skin could also lead to clogged pores and acne.

Heat therapy:
A person can use paraffin wax as a form of heat therapy for their hands or feet.
To use it for heat therapy, a person can melt the wax, test the temperature, and dip their hands or feet in it.
This may help relieve stiff muscles and joints by improving circulation and increasing blood flow to the area.
People with different forms of arthritis may find that this form of heat therapy helps alleviate pain, stiffness, and swelling, as well as helping to improve mobility and flexibility.



HOW TO USE PARAFFIN WAX:
Salons and spas may offer paraffin wax treatments, but people can also use the treatment at home.
The treatments at home and in a spa are likely very similar.
When using wax at home, a person should use caution when heating the wax and follow all instructions on the kit.

To perform a paraffin wax treatment at home, a person should follow these steps:

Wash hands with soap and water.
Apply a lotion or moisturizer to the hands.

Test the temperature of the wax by dipping a fingertip in gently.
Spread the fingers and dip the hand into the wax.
Remove when coated.

Repeat this, dipping and drying the hand about 6–8 times.
Cover the hand with a towel or plastic bag immediately.
Keep paraffin wax covered for 15–20 minutes.

Remove the towel.
Carefully peel the cooled wax from the hand.
Repeat steps with the other hand.


SAFETY INFORMATION ABOUT PARAFFIN WAX:
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product





CHEMICAL AND PHYSICAL PROPERTIES OF PARAFFIN WAX:
Chemical formula CnH2n+2
Appearance White solid
Odor Odorless
Boiling point > 370 °C (698 °F)
Solubility in water ~1 mg/L

TRADE NAMES OF PARAFFIN WAX:
IGI 1230 Paraffin Wax-Slab
IGI 1231 Paraffin Wax-Granulated
IGI 1236 Paraffin Wax -Gran
IGI 1236 Paraffin Wax-Slab
IGI 1240 Paraffin Wax-Slab
IGI 1245 Paraffin Wax-Slab
IGI 1246 Paraffin Wax-Gran
IGI 1255 Paraffin Wax-Gran
1611343 Paraffin Wax





Paraffin wax
Synonyms: Paraffin wax meets analytical specification of Ph.Eur., white, pastilles;Fully refined parafin wax Deg.56;PARAFFIN IN PASTILLE FORM 51-53 PH EUR,B;PARAFFIN IN PASTILLE FORM 52-54 PH EUR,B;PARAFFIN IN BLOCK FORM 42-44 25 KG;PARAFFIN IN BLOCK FORM 46-48 1 KG;PARAFFIN IN PASTILLE FORM 56-58 PH EUR,B;PARAFFIN IN PASTILLE FORM 57-60 PH EUR,B CAS: 8002-74-2
Paraformaldehyde
Paraform, Polyoxymethane, Formagene; Polyformaldehyde; Polyoxymethylene; Formaldehyde Polymer; Polyoxymethylene Glycol; Trioxymethylene; Paraformaldehydum; Paraformic aldehyde; Metaformaldehyde CAS:30525-89-4; 53026-80-5
PARA-FORMALDEHYDE
Para-formaldehyde is a linear polymer, cross-linking fixative that changes to formaldehyde upon heating and by adding small amount of sodium hydroxide.
Para-formaldehyde appears as a white solid with a light pungent odor.
A linear polymer of formaldehyde of formula HO(CH2-O)xH where x averages about 30.


CAS Number: 30525-89-4
EC Number: 608-494-5
MDL number: MFCD00133991
Chemical formula: OH(CH2O)nH (n = 8 - 100)


Para-formaldehyde is soluble in water when x is less than 12; higher polymers are not immediately soluble.
Slow dissolution in water of Para-formaldehyde proceeds by means of hydrolysis to give fragments of lower x.
Para-formaldehyde is the smallest polyoxymethylene, the polymerization product of formaldehyde with a typical degree of polymerization of 8–100 units.


Para-formaldehyde commonly has a slight odor of formaldehyde due to decomposition.
Para-formaldehyde is a poly-acetal.
Formaldehyde is CH2O, the simplest aldehyde.
Formalin is the name for saturated (37%) formaldehyde solution.


Thus, a protocol calling for 10% formalin is roughly equivalent to 4% formaldehyde.
Beware though, that some solutions have methanol in them to stop polymerization but this could have a negative effect on your sample.
Para-formaldehyde has actually polymerized formaldehyde. "Pure", methanol-free formaldehyde can be made by heating the solid Para-formaldehyde.
This might be called Para-formaldehyde, but Para-formaldehyde actually isn't because it’s not the polymer form.


Para-formaldehyde is the polymerization product of formaldehyde; degree of polymerization of 8–100 units.
Para-formaldehyde must be depolymerized to formaldehyde in solution prior to use since it is not the fixative itself.
The formaldehyde fixing procedure for cell samples usually involves using a 4% formaldehyde solution in phosphate buffered saline (PBS) on ice for a few minutes.


This vital step maintains the cell morphology and therefore ensures that sample cell structures stay intact, and antigens are immobilized, while still permitting antibody-target antigen access.
Para-formaldehyde depolymerizes in water to formaldehyde solution yielding consistent quality fixative solutions.
To achieve a strong solution, raise the temperature of the water to 60ºC then add sodium hydroxide solution dropwise.


Para-formaldehyde is the smallest polyoxymethylene, the polymerization product of formaldehyde with a typical degree of polymerization of 8–100 units.
Para-formaldehyde commonly has a slight odor of formaldehyde due to decomposition.
Para-formaldehyde is a poly-acetal.


Para-formaldehyde forms slowly in aqueous formaldehyde solutions as a white precipitate, especially if stored in the cold.
Formalin actually contains very little monomeric formaldehyde; most of it forms short chains of polyformaldehyde.
A small amount of methanol is often added as a stabilizer to limit the extent of polymerization.
Para-formaldehyde is as a trimer of formaldehyde and has the formula O-CH2-O-CH2-O-CH2.


Para-formaldehyde is a white, water soluble powder.
When added to a mud in advance of a bacterial inoculation and maintained, Para-formaldehyde can effectively control many strains of bacteria.
The amount or Para-formaldehyde in a mud can be estimated by oxidizing it with sulfite into formic acid and performing an alkalinity titration, according to a procedure published by API.


Para-formaldehyde is a ready-to-use fixation solution for cells or tissues.
It is electron microscopy-grade Para-formaldehyde dissolved in pH 7.4 PBS with no methanol added.
UV light and oxygen are known to cause formaldehyde degradation over long-term storage.
Biotium’s unique packaging method ensures the high quality of the formaldehyde by using amber glass vials packaged under argon gas and tightly sealed with pharmaceutical grade enclosures.


Para-formaldehyde is a general histological tissue fixative.
Contains Para-formaldehyde buffered to a neutral pH.
Para-formaldehyde is a white crystalline solid polymer with pungent odor and generates toxic formaldehyde gas when heated.
Para-formaldehyde may react violently with strong oxidizing agents and less with bases.


Para-formaldehyde is slightly soluble in alcohols and insoluble in ethers, hydrocarbons, and carbon tetrachloride.
Para-formaldehyde is a white, solid polymer of formaldehyde with the pungent, characteristic formaldehyde odor.
Para-formaldehyde is made up of connected formaldehyde molecules.
Para-formaldehyde is slightly soluble in alcohols and insoluble in ethers, hydrocarbons, and carbon tetrachloride.


Para-formaldehyde is relative insoluble in cold water, but soluble in hot water with depolymerization.
The solubility and rate of solution of Para-formaldehyde in water are greatly influenced by pH and temperature.
Both acidic and alkaline pHs and higher temperatures accelerate the rate of solution.
Once dissolved, the Para-formaldehyde solution behaves like the methanol-free formaldehyde solution of the same concentration.


Para-formaldehyde is composed of varying molecular weight polymers of polyoxymethylene glycols.
Para-formaldehyde is generally prepared as 91 or 95% formaldehyde by weight with the remainder being free and combined water.
The combined water is the terminating agent for the Para-formaldehyde chains.
Para-formaldehyde reacts chemically as formaldehyde at a rate determined by its rate of depolymerization under the conditions of use.


The rate of depolymerization and thus perceived reactivity decreases with increasing molecular weight of the polymer chains.
In microbiology laboratories, fixation process (immunofluorescence) uses formalin 4% concentration.
A blog by researchers mentioned that preparing this solution “fresh” from Para-formaldehyde is better than using formalin that has been kept for some time.


Para-formaldehyde is because more methylene glycol is present compared to its dimer and trimer oligomers and such solution of formalin 4% is absent of methanol.
Para-formaldehyde is the solid form of liquid formaldehyde, formed by the polymerization of formaldehyde with a typical degree of polymerization of 8-100 units.


Para-formaldehyde is a polymer of formaldehyde with a wide range of monomeric units typically 8-100.
Para-formaldehyde does not have the capacity to fix samples, hence it must be depolymerised in the solution.
Heating the Para-formaldehyde powder in the solution leads to its depolymerization.
Although Para-formaldehyde is widely used, there are circumstances where it is used as low as 0.5% to as high as 16%.


When dissolved, Para-formaldehyde breaks into formaldehyde in solution.
Formaldehyde fixes (halts) metabolism by cross-linking protein molecules especially with lysine.
Para-formaldehyde is important to note, that formaldehyde-based fixation is too slow and may take from a few hours to days to fix samples.
Para-formaldehyde is the polymerization product of formaldehyde with a typical degree of polymerization of 8–100 units.


Para-formaldehyde is not a fixative itself; it must be depolymerized to formaldehyde in solution.
Fixing ensures that sample cell structures stay intact and that antigens are immobilized, while ideally still permitting unfettered access of antibodies to target antigens.
Para-formaldehyde is the most preferred fixative agent as it builds covalent cross-links between molecules.


This glues them together hence effectively preserving cells and tissue components.
Use of Para-formaldehyde can guarantee consistency in the physical and chemical properties of the cell, hence no change in chemical and morphology characteristics of the cells and tissues.
Since the Para-formaldehyde is not fixative itself, it is required that formaldehyde is freshly prepared from the PFA stock.



USES and APPLICATIONS of PARA-FORMALDEHYDE:
Para-formaldehyde is used in fungicides, bactericides, and in the manufacture of adhesives.
Once Para-formaldehyde is depolymerized, the resulting formaldehyde may be used as a fumigant, disinfectant, fungicide, and fixative.
Longer chain-length (high molecular weight) polyoxymethylenes are used as a thermoplastic and are known as polyoxymethylene plastic (POM, Delrin).


Para-formaldehyde was used in the past in the discredited Sargenti method of root canal treatment.
Para-formaldehyde is not a fixative; it must be depolymerized to formaldehyde in solution.
In cell culture, a typical formaldehyde fixing procedure would involve using a 4% formaldehyde solution in phosphate buffered saline (PBS) on ice for 10 minutes.


In histology and pathology specimens preparation, usually, the fixation step is performed using 10% Neutral Buffered Formalin (4% formaldehyde) for, at least, 24 hours.
Para-formaldehyde is also used to crosslink proteins to DNA, as used in ChIP (chromatin immunoprecipitation) which is a technique to determine which part of DNA certain proteins are binding to.


Para-formaldehyde can be used as a substitute of aqueous formaldehyde to produce the resinous binding material, which is commonly used together with melamine, phenol or other reactive agents in the manufacturing of particle board, medium density fiberboard and plywood.
Para-formaldehyde is used as a methanol-free, ready-to-use fixative that functions by forming covalent cross-links between molecules.
This strong network stabilizes the cellular framework, thus effectively preserving cell and tissue components.


The fixative delivers consistency in maintaining the physical and chemical properties of the cell; no evident changes occur in the chemical and morphological characteristics of the cell/tissue specimens on exposure to the product.
Para-formaldehyde is compatible with several antibody-based detection methods, such as immunohistochemistry, immunocytochemistry, and immunofluorescence.


Para-formaldehyde is a commonly used preservative for starch, xanthan gum, guar gum and other natural polymers that are prone to attack by bacteria.
Para-formaldehyde has documented uses as a disinfectant, fungicide, fixation reagent and in the preparation of formaldehyde.
In fluorescence studies, Para-formaldehyde has been used as as a formalin fixative to fix cells and tissues.


To use the chemical as a fixative, it must be converted to the monomer formaldehyde by heating as formaldehyde is the active chemical in fixation.
Tissue specimens should be place immediately in Para-formaldehyde to prevent autolysis, putrefaction and other undesirable cellular changes.
Para-formaldehyde is required for tissue/specimen fixation.


Para-formaldehyde is used for laboratory use only.
Para-formaldehyde is a cross-linking fixative used in histology, light and electron microscopy and flow cytometry.
Para-formaldehyde is changed to formaldehyde by heating and by adding small amount of sodium hydroxide.
When the samples are to be used in fluorescence studies, Para-formaldehyde is recommended as fixative.


In histology Para-formaldehyde is generally preferred over other fixatives as the others result in more silver grains on the tissues.
Main Applications of Para-formaldehyde: Coating compounds, adhesive agent, textile-processing resins, phenol resins
Para-formaldehyde is widely used by resin manufacturers seeking low water content, or more favorable control of reaction rates when compared to aqueous formaldehyde solutions.


With less dehydration required, Para-formaldehyde resins are made in less time.
Better yields result from the complete or partial elimination of dehydration because fewer reactants are lost in the distillate.
Utility costs are reduced because Para-formaldehyde requires less steam, cooling water and power for water removal.


The capability of charging more reactants to the process equipment (in the volume otherwise occupied by water and extra azeotroping agent) increases reactor capacity, and reduces capital required for equipment versus the equipment costs and capacity when using aqueous formaldehyde.
Finally, and of increasing importance, less wastewater is produced.


Para-formaldehyde provides a source of formaldehyde for the synthesis of phenol-, urea-, furfural alcohol-, resorcinol- and melamine- formaldehyde resins.
These products find extensive usage in industrial coatings, wood products, textiles, and foundry resins.
Oil well drilling chemicals, lubricating oil additives, adhesive resins, and electrical component molding materials also use Para-formaldehyde.


Miscellaneous end uses include photographic and graphic arts chemicals, pigments, rubber antioxidants, fluorescent tube and ink chemicals, pharmaceuticals, slow release fertilizers and others.
Since Para-formaldehyde is basically a condensed form of formaldehyde, it possesses the same characteristics but with a wider range of applications.


Use of Para-formaldehyde is convenient and safe.
Para-formaldehyde avoids pollution arising from the disposal of the distillate obtained in the thermosetting resin production which is contaminated with organic matter.
Para-formaldehyde does not need to be dissolved in water in order to take part in a chemical reaction.


Para-formaldehyde eliminates the risk of transporting liquid formalin, which is notoriously dangerous.
Perfect for small uses straight from the bag.
Unlike granular or flake forms of Para-formaldehyde, our prilled form of Para-formaldehyde has higher quality consistency and higher solubility to meet with your quality requirement and save you processing time.


In coating applications, low acid content in Para-formaldehyde is important for a greater gloss control and stability.
Para-formaldehyde made with very low acid content in a chemical resistant environment can prevent formation of acidic by-products.
Para-formaldehyde can be used as a substitute of formalin to produce the resinous binding material, which is commonly used together with urea, melamine, phenol, resorcinol, tannin or other reactants in the manufacturing of particle board, fibreboard and plywood.


Para-formaldehyde is recommended to be made in 1X PBS buffer (neutral buffered formalin; NBA).
Neutral pH prevents the formation of formic acid, which is known to form "formalin pigments" in tissue and slower fixation rates.
Para-formaldehyde tissue fixation solution is widely used in the detection of tissue, tissue slice, cell and other biological sample fixation solutions such as immunohistochemistry (IHC), immunofluorescence (IF), immunocytochemistry (IC), flow cytometry (FACS).


If a lower concentration of Para-formaldehyde is needed, PBS can be used as dilution buffer.
Para-formaldehyde tissue fixation solution has strong penetrability and fixation, which can make the tissue harden and it is good for slicing.
Para-formaldehyde will cause less tissue shrinkage, less damage and mild, which can well preserve the inherent substance and maintain the antigenicity and fine structure of the tissue.


In addition, Para-formaldehyde can be used to fix and preserve fat and lipid substances.
Para-formaldehyde has good fixation effect and wide applications.
Para-formaldehyde is suitable for the fixation of various common cells or tissues.
Para-formaldehyde has good fixation effect on skin, muscle, viscera, etc.


Para-formaldehyde mainly acts on protein, but can’t fix uric acid and sugar, etc.
Para-formaldehyde does not contain DEPC and it is not recommended for in situ hybridization or other experiments requiring detection of nucleic acids.
Para-formaldehyde is prepared in PBS solution and can be directly used for tissue or cell fixation without dilution.


Para-formaldehyde is recommended that 1 ml of fixed solution is needed for each sample fixation.
In cell culture, typical formaldehyde fixing procedure would involve using a 4% formaldehyde solution in phosphate buffered saline (PBS) on ice for 10 minutes.


-Use of Para-formaldehyde in resin production offers many advantages as compared to aqueous formaldehyde:
*Higher productivity from existing equipment and less water to be removed from the resin product.
*Para-formaldehyde takes the form of prilled, is stable and very easy to store.
*Para-formaldehyde storage is less expensive than the storage of formaldehyde solution, which requires expensive tanks and which may need stabilization or be kept warm.


-Applications of Para-formaldehyde:
*Fixation solution for Immuno-histochemistry and fluorescent protein labelled samples.
*pH
*Adjust pH 6.9 to 7.4 depending on application with 1N HCl and 1N NaOH.


-Applications of Para-formaldehyde:
• for use in the preparation of formalin fixatives for tissues or cells when the samples are to be used in florescence imaging
• for fixing of cell/tissue sections during histology/staining procedures
• for cross-linking cells during chromatin immunoprecipitation (ChIP) assay


-Applications of Para-formaldehyde:
*For manufacturing of Phenolic Urea and Melamine Resins (condensation reactions).
*For production of lon Exchange Resins (chloromethylation reaction).
*Disinfection of the air in rooms.
*Hardening of Glues.
*Manufacture of fluorescent pigments and soluble condensation product for textile auxiliaries, alcoholic solutions commonly known as ‘FORMOCEL’.
*Para-formaldehyde is used in the manufacture of Phenolic Resins, of Urea, Thiourea and Melamine Formaldehyde Resins (whenever high concentration of formaldehyde is required).
*Para-formaldehyde is used in place of formaldehyde aqueous solution for high reactivity and concentrations of aldehyde contents reacted with low water contents.



FEATURES OF PARA-FORMALDEHYDE:
- Ready to use fixative buffer
- Methanol free
- Prepared from EM grade Para-formaldehyde
- Safer and more convenient than handling the Para-formaldehyde solid



WHY PARA-FORMALDEHYDE?
Para-formaldehydeafter depolymerization results in the formation of formaldehyde in solution which can be used as a fumigant, disinfectant, fungicide, fixative.
Para-formaldehyde reacts with either phenol, urea, melamine or resorcinol to produce resin.
Para-formaldehyde is also used in the production of inks of a wide array of ink applications like dollar bills, books, and other printing materials.



SYNTHESIS OF PARA-FORMALDEHYDE:
Para-formaldehyde forms slowly in aqueous formaldehyde solutions as a white precipitate, especially if stored in the cold.
Formalin actually contains very little monomeric formaldehyde; most of it forms short chains of polyformaldehyde.
A small amount of methanol is often added as a stabilizer to limit the extent of polymerization.



REACTIONS OF PARA-FORMALDEHYDE:
Para-formaldehyde can be depolymerized to formaldehyde gas by dry heating and to formaldehyde solution by water in the presence of a base, an acid or heat.
The high purity formaldehyde solutions obtained in this way are used as a fixative for microscopy and histology.
The resulting formaldehyde gas from dry heating paraformaldehyde is flammable.



DIFFERENCE BETWEEN FORMALIN, FORMALDEHYDE AND PARA-FORMALDEHYDE:
Formaldehyde is a simple aldehyde (equivalent of a monomer to Para-formaldehyde) with formula CH2O.
Formalin, on the other hand, is a saturated solution of formaldehyde (37%).
10% formalin is equivalent to 4% formaldehyde.
However, many vendors use a small amount of methanol or other chemicals to prevent polymerization of formaldehyde in the solution.
These additional reagents must be considered as they may yield unwanted effects.

Para-formaldehyde is a polymer of formaldehyde with 8-100 units.
Para-formaldehyde, when dissolved in water, breaks down into formaldehyde.
This solution differs from commercially available form (formalin) being relatively pure (devoid of methanol).
In immunohistochemistry (IHC) and cell biology experiments, researchers prefer working with Para-formaldehyde solution rather formalin due to the same reason.

Although formalin and Para-formaldehyde solutions said to be having formaldehyde, formaldehyde in these solutions is hydrated and converts (most of the formaldehyde) into methylene glycol.
In these solutions (formalin or Para-formaldehyde), a major portion of methylene glycol is in equilibrium with formaldehyde.
However, only formaldehyde (not methylene glycol) have cross-linking ability.



MAKING PARA-FORMALDEHYDE SOLUTION:
Para-formaldehyde is usually made in PBS or TBS at 70 °C with several drops of 5N NaOH to help clarify the solution.
Prepare Para-formaldehyde solution in a chemical hood if you don’t want to be slightly fixed yourself.
Often Para-formaldehyde stocks have insoluble impurities and it's best that these be removed via a quick spin in a table-top centrifuge or by passing the prepared solution through a filter syringe.
Para-formaldehyde is also important to realize that the efficacy and impurity content of powdered Para-formaldehyde can vary greatly from lot number to lot number of reagent.
Don’t be surprised if your fixation concentrations & conditions may need to be tweaked when you open a new bottle of Para-formaldehyde.



FORMALDEHYDE, FORMALIN, AND PARA-FORMALDEHYDE: WHAT'S THE DIFFERENCE?
Aldehyde fixatives act by chemically cross-linking free amine groups on proteins.
Formaldehyde is a commonly used fixative, but it is not stable in solution, because under exposure to light and oxygen it polymerizes and precipitates.
Formaldehyde solution is commonly stabilized by the addition of methanol.
The classic fixative used for pathology is 10% neutral buffered formalin, which is a solution of 10% formaldehyde in sodium phosphate buffer containing up to 1.5% methanol.

Many researchers prefer to use methanol-free formaldehyde for fixation, because methanol can permeabilize cell membranes and affect the morphology of cellular structures like the actin cytoskeleton.
To make formaldehyde solution, the polymerized Para-formaldehyde solid must be heated in basic water to form reactive formaldehyde.
Methanol-free fixative solutions prepared from Para-formaldehyde solid are commonly referred to as Para-formaldehyde solution or PFA.
While technically inaccurate, it serves to distinguish stabilizer-free formaldehyde solution from methanol-stabilized formaldehyde.



PHYSICAL and CHEMICAL PROPERTIES of PARA-FORMALDEHYDE:
Molecular Weight: 30.03 (as monomer)
Chemical formula: OH(CH2O)nH (n = 8 - 100)
Appearance: white crystalline solid
Density: 1.42 g·cm−3 (25 °C)
Melting point: 120 °C (248 °F; 393 K)
Solubility in water: low
Density: 1.49 g/cm3 (-5 °C)
Explosion limit: 7 - 73 %(V)
Ignition temperature: 300 °C
Melting Point: 164 °C
pH value: 5.5 (H₂O, 20 °C) (saturated solution)
Vapor pressure: 1.93 hPa (25 °C)
Physical state: powder
Color: No data available
Odor: pungent
Melting point/freezing point:
Melting point/range: 120 - 170 °C - lit.
Initial boiling point and boiling range: No data available
Upper/lower flammability or explosive limits:
Upper explosion limit: 73 %(V)
Lower explosion limit: 7 %(V)
Flash point: Not applicable
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: 4,0 - 5,5

Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: insoluble
Partition coefficient: n-octanol/water: No data available
Vapor pressure: No data available
Density: 0,88 g/cm3 at 25 °C - lit.
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: none
Other safety information: No data available
Formula: (CH2O)n.H2O
Decomposes at: 120-180°C
Relative density (water = 1): 1.5
Solubility in water: poor
Vapour pressure, kPa at 25°C: <0.2
Relative vapour density (air = 1): 1.03
Flash point: 71°C c.c.
Auto-ignition temperature: 300°C
Explosive limits, vol% in air: 7.0-73.0



FIRST AID MEASURES of PARA-FORMALDEHYDE:
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
Immediately call in physician.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Consult a physician.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Immediately call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of PARA-FORMALDEHYDE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Take up carefully.
Dispose of properly.



FIRE FIGHTING MEASURES of PARA-FORMALDEHYDE:
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of PARA-FORMALDEHYDE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
protective clothing.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of PARA-FORMALDEHYDE:
-Precautions for safe handling:
*Hygiene measures:
Immediately change contaminated clothing.
Apply preventive skin protection.
Wash hands and face after working with substance.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Keep locked up or in an area accessible only to qualified or authorized persons.
Storage stability:
Recommended storage temperature: 2 - 8 °C
Handle and store under inert gas.



STABILITY and REACTIVITY of PARA-FORMALDEHYDE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature).



SYNONYMS:
Paraformaldehyde
30525-89-4
Formagene
Aldacide
Flo-Mor
Polyoxymethylene glycol
Paraformic aldehyde
Polymerised formaldehyde
Y19UC83H8E
(CH2O)n
Oilstop, Halowax
Paraformaldehydum
608-494-5
Caswell No. 633
DTXSID8034798
EPA Pesticide Chemical Code 043002
HSDB 4070
Hyperband
PARAFORMALDEHYDE (MART.)
Paraforsn
UNII-Y19UC83H8E
USEPA/OPP Pesticide Code: 043002

PARAFORMALDEHYDE
4-hydroxybenzoate de propyle,Synonymes ,propylparabène parahydroxybenzoate de propyle,önipazol,paseptol,propagin,nipasol,Le 4-hydroxybenzoate de propyle ou propylparabène est un composé organique de la famille des parabènes. Il existe à l’état naturel dans de nombreuses plantes et chez quelques insectes, mais on le synthétise pour l’industrie des cosmétiques, la pharmacie et l’industrie agro-alimentaire. C’est un conservateur (E2167) que l'on trouve fréquemment dans les cosmétiques à base d’eau, comme les crèmes, lotions, shampooings et produits de bains, car il est hydrosoluble.
PARAFORMALDEHYDE 97%
Paraformaldehyde 97% Synthesis of Paraformaldehyde 97% Paraformaldehyde 97% forms slowly in aqueous formaldehyde solutions as a white precipitate, especially if stored in the cold. Formalin actually contains very little monomeric formaldehyde; most of it forms short chains of polyformaldehyde. A small amount of methanol is often added as a stabilizer to limit the extent of polymerization. Reactions of Paraformaldehyde 97% Paraformaldehyde 97% can be depolymerized to formaldehyde gas by dry heating and to formaldehyde solution by water in the presence of a base, an acid or heat. The high purity formaldehyde solutions obtained in this way are used as a fixative for microscopy and histology. The resulting formaldehyde gas from dry heating Paraformaldehyde 97% is flammable. Uses of Paraformaldehyde 97% Once Paraformaldehyde 97% is depolymerized, the resulting formaldehyde may be used as a fumigant, disinfectant, fungicide, and fixative. Longer chain-length (high molecular weight) polyoxymethylenes are used as a thermoplastic and are known as polyoxymethylene plastic (POM, Delrin). It was used in the past in the discredited Sargenti method of root canal treatment. Paraformaldehyde 97% is not a fixative; Paraformaldehyde 97% must be depolymerized to formaldehyde in solution. In cell culture, a typical formaldehyde fixing procedure would involve using a 4% formaldehyde solution in phosphate buffered saline (PBS) on ice for 10 minutes. In histology and pathology specimens preparation, usually, the fixation step is performed using 10% Neutral Buffered Formalin (4% formaldehyde) for, at least, 24 hours. Paraformaldehyde 97% is also used to crosslink proteins to DNA, as used in ChIP (chromatin immunoprecipitation) which is a technique to determine which part of DNA certain proteins are binding to. Paraformaldehyde 97% can be used as a substitute of aqueous formaldehyde to produce the resinous binding material, which is commonly used together with melamine, phenol or other reactive agents in the manufacturing of particle board, medium density fiberboard and plywood. Toxicity of Paraformaldehyde 97% As a formaldehyde releasing agent, Paraformaldehyde 97% is a potential carcinogen. Its acute oral median lethal dose in rats is 592 mg/kg. Properties of Paraformaldehyde 97% Chemical formula OH(CH2O)nH (n = 8 - 100) Appearance white crystalline solid Density 1.42 g·cm−3 (25 °C) Melting point 120 °C (248 °F; 393 K) Solubility in water low General description of Paraformaldehyde 97% Paraformaldehyde 97% is also referred as polyoxymethylene. Paraformaldehyde 97% participates as an external CO source in the synthesis of aromatic aldehydes and esters. Paraformaldehyde is an ideal fixative used in histology. Paraformaldehyde 97% is generally preferred over other fixative as the others result in more silver grains on the tissues. Paraformaldehyde 97%, appropriately combined with DMSO (dimethyl sulfoxide) ensures its uniform distribution over the tissue section. Paraformaldehyde is also used in recognizing and stabilizing the expression of intracellular antigen. Application of Paraformaldehyde 97% Paraformaldehyde 97% has been used as a fixative in histological analysis. Paraformaldehyde 97% has also been used in mitotic catastrophe assay. Paraformaldehyde 97% is the informal name of polyoxymethylene, a polymer of formaldehyde (also known by many other and confusing names, such as ‘paraform’, ‘formagene’, ‘para’, ‘polyoxymethane’). Paraformaldehyde 97% is the informal name of polyoxymethylene, a polymer of formaldehyde (also known by many other and confusing names, such as ‘paraform’, ‘formagene’, ‘para’, ‘polyoxymethane’). It is slowly formed as a white precipitate by condensation from the predominant species methanediol (formaldehyde hydrate) in solutions of formaldehyde (which may also be called ‘formalin’, ‘formal’, or ‘formalose’) on standing, in an equilibrium (Fig. 3.1). The solution is predominantly of oligomers, but when n becomes large enough the material becomes sufficiently insoluble as to precipitate, when the condensation may still continue. The resulting solid may have n range from ~ 8 to 100, or more. The reaction is driven to the left, to release formaldehyde, by a low concentration of formaldehyde, and accelerated by acidic or alkaline conditions. Solid Paraformaldehyde 97% smells plainly of the monomer (b.p. − 21 °C), so it is essentially a convenient means of delivering formaldehyde slowly. Paraformaldehyde 97% has documented uses as a disinfectant, fungicide, fixation reagent and in the preparation of formaldehyde. In fluorescence studies, paraformaldehyde 97% has been used as as a formalin fixative to fix cells and tissues. To use the chemical as a fixative, it must be converted to the monomer formaldehyde by heating as formaldehyde is the active chemical in fixation. Paraformaldehyde 97% is a polymer of formaldehyde. Paraformaldehyde 97% itself is not a fixing agent, and needs to be broken down into its basic building block formaldehyde. This can be done by heating or basic conditions until it becomes solubilized. Once that occurs, essentially they are exactly the same. Beware though, some commerical formaldehyde solutions contain methanol to prevent polymerization (into Paraformaldehyde 97%), and this methanol can potentially inhibit your experiment. We allow Paraformaldehyde 97% to heat over-night, filter, and use fresh for our fixation protocols for immunofluorescence, and we have great success. We store the Paraformaldehyde 97% in the fridge, but do not use it after a few days because it will eventually polymerize again and become less efficacious. A polymer consists of 10 to 100 formaldehyde units. Not only the hazardous effects to human health and environment but also the difficulties in processing and storing of formaldehyde gas leads to paraformaldehyde use in formaldehyde resins. Paraformaldehyde decomposes into the formaldehyde at nearly 150°C. Paraformaldehyde 97% applications Applications The most important use of Paraformaldehyde 97% is as a source of formaldehyde groups in the production of many thermosetting resins, together with phenol, urea, melamine, resorcinol and other similar reagents. These resins are used as moulding powders; in the wood industry as glues for chipboard, plywood and furniture; as bonding resins for brakes, abrasives and foundry dyes; as finishing resins for paper and textiles; as driers and glossing agents for paints; as insulating varnishes for electrical parts. Some typical formulations for the production of such resins starting from Paraformaldehyde 97% include dichloroethyl formal, methyl phenol, disinfectants, insecticides, pharmaceuticals such as vitamin A, embalming preparations, dyestuff and special plasticizers. In addition, Paraformaldehyde 97% is used as a fungicide and bactericide in industries as varied as crude oil production, beet sugar refining, and warehousing. Paraformaldehyde 97% has widespread acceptance as an additive to stop fermentation of the starch on oil-well-drilling muds. The sugar beet industry used it to minimize the growth of algae in its continuous diffusers. Hotels and motels in humid areas often use it, with or without added mothproofing agents, in small bags hung in closets to prevent the formation of mildew. Paraformaldehyde 97% possesses the common characteristics with a wide range of applications Paraformaldehyde 97% is the smallest solid form of liquid formaldehyde, formed by the polymerization of formaldehyde with a typical degree of polymerization of 8-100 units. As Paraformaldehyde 97% is basically a condensed form of formaldehyde, it possesses the common characteristics with a wide range of applications. Advantages of Paraformaldehyde 97% in resin production as compared to aqueous formaldehyde Paraformaldehyde 97% does not need to be dissolved in water in order to take part in a chemical reaction. Higher productivity from existing equipment and less water to be removed from the resin product. Paraformaldehyde 97% made with very low acid content in a chemical resistant environment can prevent the formation of acidic by-products. We offer a prilled form, which is stable and very easy to store. Paraformaldehyde 97% storage is less expensive than the storage of formaldehyde solution, which requires expensive tanks and which may need stabilization or be kept warm. It eliminates the risk of transporting liquid formalin, which is notoriously dangerous. Perfect for small uses straight from the bag. Use of Paraformaldehyde 97% is convenient and safe. It avoids pollution arising from the disposal of the distillate obtained in the thermosetting resin production which is contaminated with organic matter. Typical Properties of Paraformaldehyde 97% Color White CAS Number 30525-89-4 Appearance Free Flowing Prilled Molecular Formula OH-(CH2O)n-H where n=8 to 100 units Paraformaldehyde 97% Content 92% ± 1% / 96% ± 1% Water Content 8% ± 1% / 4% ± 1% Reactivity 2 – 8 min Mean Particle Size 250 – 350 µm Ash 0.01 – 0.05% Bulk Density 650 – 850 kg/m3 Melting Point 120 – 175 C Ph 4 – 7 Flammability combustible, with flash point (tag open cup) of about 93 C Vapour Pressure varies with air humidity, being between 23 and 26 mmHg at 25 C Applications of Paraformaldehyde 97% Resins Industry The most important use of Paraformaldehyde 97% is as a source of formaldehyde groups in the production of many thermosetting resins, together with phenol, urea, melamine, resorcinol and other similar reagents. These resins are used as moulding powders; in the wood industry as glues for chipboard, plywood and furniture; as bonding resins for brakes, abrasives and foundry dyes; as finishing resins for paper and textiles; as driers and glossing agents for paints; as insulating varnishes for electrical parts. Disinfectant Paraformaldehyde 97% generates formaldehyde gas when it is depolymerized by heating. The depolymerized material reacts with the moisture in the air to form formaldehyde gas. This process is used for the decontamination of large spaced and laminar-flow biological safety cabinets when maintenance work or filter changes require access to the sealed portion of the cabinet. It is used in the poultry industry as a disinfectant in the hatcheries, and cattle and sheep industry for sanitizing the bedding in the sheds. It releases formaldehyde gas when the temperatures increase. It reduces contamination levels caused by moulds, viruses and bacteria. Agriculture and Pesticides Most Paraformaldehyde 97% consumed by the agrochemicals industry is for the herbicides such as bismerthiazol, butachlor, acetochlor, glyphosate, and machete. Embalming Process Formalin is used during embalming processes as a disinfectant and preservative. It is used as an injection fluid in arterial and cavity embalming, and in surface embalming as a fluid for soaking surface packs or a gel applied to the skin or internal surfaces. Paraformaldehyde 97%, a powdered polymer form of formaldehyde, is also sometimes used in embalming processes. Reagent for Organic Reactions In microbiology laboratories, fixation process (immunofluorescence) uses formalin 4% concentration. A blog by researchers mentioned that preparing this solution “fresh” from Paraformaldehyde 97% is better than using formalin that has been kept for some time. It is because more methylene glycol is present compared to its dimer and trimer oligomers and such solution of formalin 4% is absent of methanol. Oil Well Drilling Chemicals Paraformaldehyde 97% is used in the manufacturing of 1,3,5-triazine used as H2S scavenger in Oil drilling process. Paraformaldehyde 97% tablets are very effective against a wide spectrum of organisms. They may be recommended for targeted degerming measures in medical practice. Their utilization requires the observance of the conditions necessary for their efficient use. The tablets should be employed only in containers which are as tight-fitting as possible (preferentially instrument cabinets, Heynemann cabinets, catheter boxes and plastic bags). Paraformaldehyde 97% tablets are well suited for the reduction of the bacterial population and the storage of nonwrapped sterilized instruments. For this purpose, 1 tablet/dm3 is needed. The exposure time required for bacterial count reduction is no less than 3 h. Despite certain limitations, Paraformaldehyde 97% tablets may be used for disinfecting. The objects to be disinfected should be neither too contaminated nor too soiled. The minimum period of exposure is 5 h, and 10 tablets/dm3 are necessary. Cold sterilization requires 10 tablets/dm3, too; but the exposure time ranges from 15 to 24 h. This method (which must be considered an expedient) should be employed only if the respective device or instrument cannot be sterilized by other sterilizing techniques. In any case, 80% relative air humidity is a must in the devices in which Paraformaldehyde 97% tablets are used. Paraformaldehyde 97% is the solid form of liquid formaldehyde, formed by the polymerization of formaldehyde with a typical degree of polymerization of 8-100 units. Since Paraformaldehyde 97% is basically a condensed form of formaldehyde, it possesses the same characteristics but with a wider range of applications. Manufactured based on the latest technology to give good solubility, homogeneous prilled and low acid content, it is suitable for all ranges of application of Paraformaldehyde 97%. Unlike granular or flake forms of Paraformaldehyde 97%, our prilled form of Paraformaldehyde 97% has higher quality consistency and higher solubility to meet with your quality requirement and save you processing time. In coating applications, low acid content in Paraformaldehyde 97% is important for a greater gloss control and stability. Paraformaldehyde 97% made with very low acid content in a chemical resistant environment can prevent formation of acidic by-products. In microbiology laboratories, fixation process (immunofluorescence) uses formalin 4% concentration. A blog by researchers mentioned that preparing this solution “fresh” from Paraformaldehyde 97% is better than using formalin that has been kept for some time. It is because more methylene glycol is present compared to its dimer and trimer oligomers and such solution of formalin 4% is absent of methanol. Paraformaldehyde 97% can be used as a substitute of formalin to produce the resinous binding material, which is commonly used together with urea, melamine, phenol, resorcinol, tannin or other reactants in the manufacturing of particle board, fibreboard and plywood. Use of Paraformaldehyde 97% in resin production offers many advantages as compared to aqueous formaldehyde: Higher productivity from existing equipment and less water to be removed from the resin product. It takes the form of prilled, is stable and very easy to store. Paraformaldehyde 97% storage is less expensive than the storage of formaldehyde solution, which requires expensive tanks and which may need stabilization or be kept warm. Use of Paraformaldehyde 97% is convenient and safe. It avoids pollution arising from the disposal of the distillate obtained in the thermosetting resin production which is contaminated with organic matter. Paraformaldehyde 97% does not need to be dissolved in water in order to take part in a chemical reaction. It eliminates the risk of transporting liquid formalin, which is notoriously dangerous. Perfect for small uses straight from the bag. Packaging & Handling of Paraformaldehyde 97% - Polyethylene bag : 25 KG nett. Other Packaging sizes by request. - Keep in a dry, cool and well-ventilated place. Provide sufficient air exchange and/or exhaust in work rooms. Paraformaldehyde 97% decomposes to formaldehyde which can build up in a shipping container depending on time and temperature during transit. The level of formaldehyde exposure may be instantaneously high when the shipping container is opened. Storage of Paraformaldehyde 97% Store in locked up. Location of storage should only be accesible to authorised personnel. Separate storage area from work place. By Application of Paraformaldehyde 97% Urea-Formaldehyde Resin Phenolic Resin Melamine Resin Fumigation Reagent for organic reactions Coating Pesticide Disinfectant Pharmaceuticals Paraformaldehyde 97% (PFA) is a polymer of formaldehyde. Paraformaldehyde 97% itself is not a fixing agent, and needs to be broken down into its basic building block, formaldehyde. This can be done by heating or basic conditions until it becomes solubilized. Formalin is the name for saturated (37%) formaldehyde solution. Beware though, some commercial formaldehyde solutions contain methanol to prevent polymerization (into Paraformaldehyde 97%). Since 100% formalin contains up to 15% of methanol as a stabilizer, it has a significant impact on cell fixation. Methanol is a permeabilizing agent. It can interfere with the staining of membrane bound proteins, and can greatly influence staining of cytoskeletal proteins. For example, when staining cellular F-actin it is imperative to use a methanol-free formaldehyde fixative. This is because methanol can disrupt F-actin during the fixation process and prevent the binding of phalloidin conjugates. "Pure" methanol-free formaldehyde can be made by heating the solid PFA. 4% Paraformaldehyde 97% is usually made in PBS or TBS at 70 °C with several drops of 5N NaOH to help clarify the solution. Prepare 4% Paraformaldehyde 97% solution in a chemical hood and then store in a refrigerator. Because the solution will re-polymerize during storage it is best to use immediately or within a few days. In the presence of air and moisture, polymerization readily takes place in concentrated solutions at room temperatures to form paraformaldehyde, a solid mixture of linear polyoxymethylene glycols containing 90-99% formaldehyde. Paraformaldehyde 97% is used in place of aqueous formaldehyde solutions, especially in applications where the presence of water interferes, e.g., in the plastics industry for the preparation of phenol, urea, and melamine resins, varnish resins, thermosets, and foundry resins. Other uses include the synthesis of organic products in the chemical and pharmaceutical industries (e.g., Prins reaction, chloromethylation, Mannich reaction), the production of textile auxiliaries (e.g., for crease-resistant finishes), and the preparation of disinfectants and deodorants. Paraformaldehyde 97% is prepared industrially in continuously operated plants by concentrating aqueous formaldehyde solutions under vacuum conditions. ... /It/ is currently produced in several steps which are carried out at low pressure and various temperatures. Highly reactive formaldehyde is produced under vacuum conditions starting with solutions that contain 50 - 100 ppm of formic acid and also 1 - 15 ppm of metal formates where the metals have an atomic number of 23 - 30 (e.g., Mn, Co, and Cu). The solutions are processed in thin-layer evaporators and spray dryers. Other techniques such as fractional condensation of the reaction gases in combination with the formaldehyde synthesis process and very rapid cooling of the gases are also applied. Alternatively, formaldehyde-containing gas is brought into contact with Paraformaldehyde 97% at a temperature that is above the dew point of the gas and below the decomposition temperature of Paraformaldehyde 97%. The product is obtained in the form of flakes when a highly concentrated formaldehyde solution is poured onto a heated metal surface. The hardened product is subsequently scraped off and thoroughly dried. Paraformaldehyde 97% beads are produced by introducing a highly concentrated melt into a cooling liquid (e.g., benzene, toluene, cyclohexane). Acids and alkalis are also added; they apparently accelerate polymerization and lead to the formation of higher molecular mass but less reactive Paraformaldehyde 97%. Highly soluble, highly reactive Paraformaldehyde 97% with a low degree of polymerization is very much in demand. It is produced from concentrated, aqueous - alcoholic formaldehyde solutions. Dental Paraformaldehyde 97% Paste (Jap P). Past. Paraform. Dent. Paraformaldehyde 97% 35 g, procaine hydrochloride 35 g, hydrous wool fat 30 g. The widmark test for the UV photometric determination of ethanol in blood and urine is described. Paraformaldehyde 97% can also be detected. Paraformaldehyde 97% is designated as a hazardous substance under section 311(b)(2)(A) of the Federal Water Pollution Control Act and further regulated by the Clean Water Act Amendments of 1977 and 1978. These regulations apply to discharges of this substance. This designation includes any isomers and hydrates, as well as any solutions and mixtures containing this substance. The Agency has completed its assessment of the residential, occupational and ecological risks associated with the use of pesticide products containing the active ingredient formaldehyde and Paraformaldehyde 97%. The Agency has determined that virtually all formaldehyde and Paraformaldehyde 97% containing products are eligible for reregistration provided that: 1) all risk mitigation measures are implemented; 2) current data gaps and confirmatory data needs are addressed; and 3) label amendments are made as described in Section V. Use in confined spaces such as closets is not eligible for registration because of the difficulty associated with ventilation of these spaces. ... Based on its evaluation of formaldehyde and Paraformaldehyde 97%, the Agency has determined that formaldehyde and Paraformaldehyde 97% products, unless labeled and used as specified in this document, would present risks inconsistent with FIFRA. Accordingly, should a registrant fail to implement the risk mitigation measures, submit confirmatory data as well as make the label changes identified in this document, the Agency may take regulatory action to address the risk concerns from the use of formaldehyde and Paraformaldehyde 97%. If all changes outlined in this document are fully complied with, then no risks of concern exist for the registered uses of formaldehyde and Paraformaldehyde 97% and the purposes of this determination. The Agency has completed its assessment of the residential, occupational and ecological risks associated with the use of pesticide products containing the active ingredient formaldehyde and Paraformaldehyde 97%. The Agency has determined that virtually all formaldehyde and Paraformaldehyde 97% containing products are eligible for reregistration provided that: 1) all risk mitigation measures are implemented; 2) currentdata gaps and confirmatory data needs are addressed; and 3) label amendments are made as described in Section V. Use in confined spaces such as closets is not eligible for registration because of the difficulty associated with ventilation of these spaces. ... Based on its evaluation of formaldehyde and Paraformaldehyde 97%, the Agency has determined that formaldehyde and Paraformaldehyde 97% products, unless labeled and used as specified in this document, would present risks inconsistent with FIFRA. Accordingly, should a registrant fail to implement the risk mitigation measures, submit confirmatory data as well as make the label changes identified in this document, the Agency may take regulatory action to address the risk concerns from the use of formaldehyde and Paraformaldehyde 97%. If all changes outlined in this document are fully complied with, then no risks of concern exist for the registered uses of formaldehyde and Paraformaldehyde 97% and the purposes of this determination. As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their continued use. Under this pesticide reregistration program, EPA examines newer health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether the use of the pesticide does not pose unreasonable risk in accordance to newer saftey standards, such as those described in the Food Quality Protection Act of 1996. Paraformaldehyde 97% is found on List A, which contains most pesticides that are used on foods and, hence, have a high potential for human exposure. List A consists of the 194 chemical cases (or 350 individual active ingredients) for which EPA issued registration standards prior to FIFRA '88. Case No: 0556; Pesticide type: fungicide, antimicrobial; Registration Standard Date: 05/31/88 PB88-231543; Case Status: OPP is reviewing data from the pesticide's producers regarding its human health and/or environmental effects, or OPP is determining the pesticide's eligibility for reregistration and developing the Reregistration Eligibility Decision (RED) document.; Active ingredient (AI): Paraformaldehyde 97%; AI Status: The producers of the pesticide have made commitments to conduct the studies and pay the fees required for reregistration, and are meeting those commitments in a timely manner. Paraformaldehyde 97% is an indirect food additive for use only as a component of adhesives. More decay was associated with tapholes in mature sugar maples (Acer saccharum) treated with a 250-mg Paraformaldehyde 97% pill than with control tapholes. This was apparent 20 months after treatment and at each successive examination to the final measurement at 56 months. Repeated use of Paraformaldehyde 97% leads to rapid development of decay in sugar maple. Paraformaldehyde 97% is listed as a synthetic organic chemical which should be degradable by biological sewage treatment provided suitable acclimatization can be achieved. Paraformaldehyde 97% is ubiquitous in the environment; it is an chemical that occurs in most life forms, including humans. It is formed naturally in the troposphere during the oxidation of hydrocarbons. Paraformaldehyde 97%'s production and use in the manufacture of a wide range of chemicals, such as resins, finding a variety of end uses such as wood products, plastics, and coatings may result in its release to the environment through various waste streams. Its use as a fumigant in agricultural premises and as a surface disinfectant in commercial premises and its use as a corrosion inhibitor in oil wells and release from slow-release fertilizers result in its direct release to the environment. If released to air, a vapor pressure of 3,890 mm Hg at 25 °C indicates Paraformaldehyde 97% will exist solely as a gas in the atmosphere. Gas-phase Paraformaldehyde 97% will be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is 45 hrs. Paraformaldehyde 97% absorbs ultraviolet radiation at wavelengths of >360 nm and is susceptible to direct photolysis. Paraformaldehyde 97% has a direct photolysis half-life of 4.1 hours measured at sea-level and 40 degrees latitude. Paraformaldehyde 97% has been detected in rainwater and adsorbed to atmospheric particulates indicating it may be removed from the air by wet and dry deposition. If released to soil, Paraformaldehyde 97% is expected to have very high mobility based upon an estimated Koc of 8. In soil, Paraformaldehyde 97% gas can adsorb to clay minerals and interact with humic substances resulting in decreased mobility. Volatilization from moist soil surfaces is not expected to be an important fate process based upon a Henry's Law constant of 3.37X10-7 atm-cu m/mole. Paraformaldehyde 97% will volatilize from dry soil surfaces based upon its vapor pressure. Paraformaldehyde 97% has been found to be readily biodegradable in various screening tests. Utilizing the Japanese MITI test, 91% of the Theoretical BOD was reached in 2 weeks indicating that biodegradation is an important environmental fate process in soil and water. If released into water, Paraformaldehyde 97% is not expected to adsorb to suspended solids and sediment based upon the estimated Koc. In a die-away test using water from a stagnant lake, degradation was complete in 30 and 40 hrs under aerobic and anaerobic conditions, respectively. The half-life of Paraformaldehyde 97% has been reported between 1-7 days in surface water and 2-14 days in groundwater, based on estimated aqueous aerobic biodegradation half lives. Volatilization from water surfaces is not expected to be an important fate process based upon this compound's Henry's Law constant. An estimated BCF of 3 suggests the potential for bioconcentration in aquatic organisms is low. Paraformaldehyde 97% is not expected to undergo hydrolysis in the environment because of the lack of hydrolyzable functional groups. Occupational exposure to Paraformaldehyde 97% may occur through inhalation and dermal contact with this compound at workplaces where Paraformaldehyde 97% is produced or used. Monitoring data indicate that the general population may be exposed to Paraformaldehyde 97% via inhalation of ambient air (indoor and outdoor), inhalation of cigarette smoke, ingestion of food and possibly drinking water, and dermal contact with cosmetics, aerosol products and other consumer products containing Paraformaldehyde 97%. Concentrations of Paraformaldehyde 97% in outdoor and indoor air range from about 1 to 20 ug/cu m and 25 to 100 ug/cu m, respectively. Paraformaldehyde 97% is ubiquitous in the environment; it is an endogenous chemical that occurs in most life forms, including humans. It is formed naturally in the troposphere during the oxidation of hydrocarbons, which react with hydroxyl radicals and ozone to form Paraformaldehyde 97% and other aldehydes, as intermediates in a series of reactions that ultimately lead to the formation of carbon monoxide and carbon dioxide, hydrogen and water. Of the hydrocarbons found in the troposphere, methane is the single most important source of Paraformaldehyde 97%. Terpenes and isoprene, emitted by foliage, react with hydroxyl radicals, forming Paraformaldehyde 97% as an intermediate product. Because of their short half-life, these potentially important sources of Paraformaldehyde 97% are important only in the vicinity of vegetation. Paraformaldehyde 97% is one of the volatile compounds formed in the early stages of decomposition of plant residues in the soil. Paraformaldehyde 97% occurs naturally in fruits and other foods. Other sources are forest fires, animal wastes, microbial products of biological systems, and plant volatiles(2,3). Paraformaldehyde 97% can also be formed in seawater by photochemical processes. However, calculations of sea-air exchange indicates that this process is probably a minor source for Paraformaldehyde 97% in the sea. Paraformaldehyde 97%'s production and use in the manufacture of a wide range of chemicals, such as resins, finding a variety of end uses such as wood products, plastics, and coatings may result in its release to the environment through various waste streams. Its use as a fumigant in agricultural premises and as a surface disinfectant in commercial premises and its use as a corrosion inhibitor in oil wells and release from slow-release fertilizers result in its direct release to the environment. Paraformaldehyde 97% is formed by the incomplete combustion of many organic substances and is present in coal and wood smoke and in cigarette smoke. Based on a classification scheme, an estimated Koc value of 8, determined from a log Kow of 0.35 and a regression-derived equation, indicates that Paraformaldehyde 97% is expected to have very high mobility in soil. In soil, Paraformaldehyde 97% gas can adsorb to clay minerals and interact with humic substances resulting in decreased mobility. Volatilization of Paraformaldehyde 97% from moist soil surfaces is not expected to be an important fate process given a Henry's Law constant of 3.37X10-7 atm-cu m/mole. Paraformaldehyde 97% is expected to volatilize from dry soil surfaces based upon a vapor pressure of 3,890 mm Hg at 25 °C. Paraformaldehyde 97% has been found to be readily biodegradable in various screening tests. Utilizing the Japanese MITI test, 91% of the Theoretical BOD was reached in 2 weeks indicating that biodegradation is an important environmental fate process in soil.
PATCAT 3020
Patcat 3020 is a clear yellow viscous liquid.
Patcat 3020 is an organotin compound.


CAS Number: 77-58-7
EC Number: 201-039-8
MDL number: MFCD00008963
Chemical Name: Dibutyltin dilaurate
Molecular Formula: C32H64O4Sn / (C4H9)2Sn(OOC(CH2)10CH3)2



SYNONYMS:
Dibutyl(dodecanoyloxy)stannyl dodecanoate, Butynorate, Davainex, DBTDL, DBTL, Dibutylbis(lauroyloxy)tin, Dibutylstannylene dilaurate, Dibutyltin didodecanoate, Dibutyltindilaurate, Lauric acid, 1,1'-(dibutylstannylene) ester, Stabilizer D-22, T 12 (catalyst), Tinostat, Dibutyltin dilaurate, 77-58-7, Stanclere DBTL, Dibutyltin laurate, Di-n-butyltin dilaurate, Dibutylbis(lauroyloxy)tin, Stavinor 1200 SN, Dibutyltin n-dodecanoate, Ongrostab BLTM, Fomrez sul-4, Dibutylstannylene dilaurate, Thermolite T 12, Mark 1038, Bis(lauroyloxy)di(n-butyl)stannane, Kosmos 19, Therm chek 820, Stannane, dibutylbis[(1-oxododecyl)oxy]-, TIN DIBUTYL DILAURATE, Dibutyl-zinn-dilaurat, Neostann U 100, Tin, dibutylbis(lauroyloxy)-, Lankromark LT 173, TVS-TL 700, Dibutylstannium dilaurate, Stannane, bis(lauroyloxy)dibutyl-, Stannane, dibutylbis(lauroyloxy)-, Laudran di-n-butylcinicity, [dibutyl(dodecanoyloxy)stannyl] dodecanoate, Lauric acid, dibutylstannylene salt, Lauric acid, dibutyltin deriv., dibutylstannanediyl didodecanoate, Stannane, bis(dodecanoyloxy) di-n-butyl-, T 12, KS 20, TN 12, Tin, di-n-butyl-, di(dodecanoate), Dibutylbis(1-oxododecyl)oxy)stannane, Lauric acid, dibutylstannylene deriv., Dodecanoic acid, 1,1'-(dibutylstannylene) ester, Laustan-B, CAS-77-58-7, Dibutyl-tin-dilaurate, TN 12 (catalyst), Stavincor 1200 SN, Mark BT 11, Mark BT 18, Dibutylbis(lauroxy)stannane, Butyl norate, CCRIS 4786, DXR 81, HSDB 5214, T 12 (VAN), Stabilizer D 22, NSC 2607, SM 2014C, EINECS 201-039-8, Dibutyltin dillaurate, Metacure T-12, Stannane, bis(dodecanoyloxy)di-n-butyl, Tin, di(dodecanoate), di-n-Butylin dilaurate, AI3-26331, ADK STAB BT-11, Dibutyltin dilaurate, 95%, UNII-L4061GMT90, DTXSID6024961, NSC2607, Lauric acid, dibutyltin derivative, Dibutylbis(1-oxododecyloxy)stannane, Bis(dodecanoyloxy)di-n-butylstannane, Tox21_112324, Dibutyl[bis(dodecanoyloxy)]stannane #, Dibutyltin dilaurate, SAJ first grade, Tox21_112324_1, ZINC169743348, Dibutyltin dilaurate, Selectophore(TM), WLN: 11VO-SN-4&4&OV11, Lauric acid, dibutylstannylene derivative, NCGC00166115-02, Di-n-butyltin dilaurate (18 - 19% Sn), FT-0624688, E78905, EC 201-039-8, A839138, Q-200959, dodecanoic acid [dibutyl(1-oxododecoxy)stannyl] ester, Dibutylbis(lauroyloxy)stannane, Dibutyl bis(lauroyloxy)tin, Dibutylzinnbislaurat, Butylzinn Dilaurat, Dibutylbis (lauroyloxy) stannan, Dibutylbis ((1-oxododecyl)oxy)stannan, DBTDL, DBTL, DI-N-BUTYLDILAURYLTIN, DI-N-BUTYLTIN DILAURATE, DIBUTYLBIS(LAUROYLOXY)STANNANE, DIBUTYLBIS(LAUROYLOXY)TIN, DIBUTYLTIN DIDODECANOATE, DIBUTYLTIN DILAURATE, DIBUTYLTIN(IV) DILAURATE, DIBUTYLTIN LAURATE, DBTDL, Dabco T-12, DBTL, Bis(lauroyloxy)di(n-butyl)stannane, Butynorate, Cata-Chek 820, DBTL, DXR 81, Davainex, Di-n-butyltin dilaurate, Dibutyl-tin-dilaurate, Dibutyl-zinn-dilaurat, Dibutylbis(laurato)tin, Dibutylbis(lauroxy)stannane, Dibutylbis(lauroyloxy)tin, Dibutylstannium dilaurate, Dibutylstannylene dilaurate, Dibutyltin didodecanoate, Dibutyltin laurate, Dibutyltin n-dodecanoate, Fomrez sul-4, KS 20, Kosmos 19, Lankromark LT 173, Laudran di-n-butylcinicity, Lauric acid, dibutylstannylene deriv., Lauric acid, dibutylstannylene salt, Lauric acid, dibutyltin deriv., Laustan-B, Mark 1038, Mark BT 11, Mark BT 18, Neostann U 100, Ongrostab BLTM, SM 2014C, Stabilizer D-22, Stanclere DBTL, Stannane, bis(dodecanoyloxy) di-n-butyl-, Stannane, bis(dodecanoyloxy)di-n-butyl, Stannane, bis(lauroyloxy)dibutyl-, Stannane, dibutylbis((1-oxododecyl)oxy)-, Stannane, dibutylbis(lauroyloxy)-, Stavincor 1200 SN, Stavinor 1200 SN, T 12, T 12 (VAN), T 12 (catalyst), TN 12, TN 12 (catalyst), TVS Tin Lau, TVS-TL 700, Therm chek 820, Thermolite T 12, Tin dibutyl dilaurate, Tin, di-n-butyl-, di(dodecanoate), Tin, dibutylbis(lauroyloxy)-, Tinostat, UN2788 (liquid), UN3146 (solid), Aids010213, Aids-010213, DBTDL, Aids010213, Aids-010213, Ditin butyl dilaurate(dibutyl bis((1-oxododecyl)oxy)-Stannane), dibutyltin(IV) dodecanoate, Two dibutyltin dilaurate, The two butyltintwo lauricacid, Dibutyltin dilaurate 95%, DBTDL, dbtl, t12, tn12, davainex, tinostat, butynorate, DI-N-BUTYLTIN DILAURATE, Dibutyltin dilaurate 95%, bis(lauroyloxy)dibutyl-stannan, Di-N-butyldilauryltin, Dibutylbis(lauroyloxy)tin, DBTDL, Ditin butyl dilaurate(dibutyl bis((1-oxododecyl)oxy)-Stannane), dibutyltin(IV) dodecanoate, Two dibutyltin dilaurate, The two butyltintwo lauricacid;Dibutyltin dilaurate 95%, Bis(lauroyloxy)di(n-butyl)stannane, Di-n-butylin dilaurate, Di-n-butyltin dilaurate, Dibutylbis(1-oxododecyl)oxy)stannane, Dibutylbis(laurato)tin, Dibutylbis(lauroxy)stannane, Dibutylbis(lauroyloxy)tin, Dibutylstannium dilaurate, Dibutylstannylene dilaurate, Dibutyltin didodecanoate, DBTL, BT-25, dibutyltin dodecanoate, Dibutyltin Laurate, Dibutyltindilaurate, Dibutyltin Dilaurate, Di-n-butyldilauryltin, Di-N-Butyltin Dilaurate, Dibutyltin(Iv) Dilaurate, Dibutyltin Didodecanoate, Dibutylbis(Lauroyloxy)Tin, dibutyl(didodecyl)stannane, Dibutylbis(Lauroyloxy)Stannane



Patcat 3020 is an organotin compound that is used as a catalyst.
Patcat 3020 is a colourless oily liquid.
In terms of its structure, the molecule of Patcat 3020 consists of two laurate groups attached to a dibutyltin(IV) center.


Patcat 3020 is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 100 to < 1 000 tonnes per annum.
Patcat 3020 is a clear yellow viscous liquid.


Patcat 3020 is an organotin compound.
Tin is a chemical element with the symbol Sn and atomic number 50.
It is a natural component of the earth's crust and is obtained chiefly from the mineral cassiterite, where it occurs as tin dioxide.


Patcat 3020, knon as Dibutyltin dilaurate, is a clear, and yellowish liquid.
If solidification occurs, Patcat 3020 should be warmed to melt, if done so, no loss of activity will occur.
Patcat 3020 is an organotin compound with the formula (CH3(CH2)10CO2)2Sn(CH2CH2CH2CH3)2.


Patcat 3020 is a colorless viscous and oily liquid.
In terms of its structure, the molecule of Patcat 3020 consists of two laurate groups and two butyl groups attached to a tin(IV) atom.
The molecular geometry of Patcat 3020 at tin is tetrahedral.


Based on the crystal structure of the related bis(bromobenzoate), the oxygen atoms of the carbonyl groups are weakly bonded to tin atom.
According to some authors, Patcat 3020 is a dibutyltin(IV) ester of lauric acid.



USES and APPLICATIONS of PATCAT 3020:
Patcat 3020 can be used as PVC heat stabilizers, and it is the earliest used varieties in organotin stabilizers, heat resistance is less than tributyltin maleate, but it has excellent lubricity, weather resistance and transparency can be ok, and it has good compatibility with plasticizers, non-blooming, non-sulfide pollution, no adverse effects on heat sealing and printability.


Patcat 3020 is mainly used in soft transparent products or semi-soft products, generally in an amount of 1-2%.
In hard products, Patcat 3020 can be used as lubricant, and when used with maleic acid organic tin or thiol-containing organic tin can improve the fluidity of the resin material.


For Patcat 3020 is liquid at room temperature, so the dispersion in plastic is better than solid stabilizer.
Compared with other organic tin, the goods early color large will cause yellow discoloration.
Patcat 3020 can also be used as catalysts of synthesizing polyurethane, the curing agents of silicone rubber.


In order to enhance the thermal stability, transparency, compatibility with resins, as well as improve the impact strength for hard products and its other properties, now Patcat 3020 has developed a number of modified varieties.
Lauric acid and other fatty acids is generally added in the category of pure, the epoxy ester or other metal soap stabilizer is also added in.


Patcat 3020 is used as a catalyst in the synthesis of polyurethane foams.
Patcat 3020 has excellent transparency and lubricating property.
Patcat 3020 is resistant to weathering.


Patcat 3020 can also uesd the stabilizer of the soft transparent products and efficient lubricants in hard transparent products, and can also be used acrylate rubber and rubber carboxyl crosslinking reaction, the catalyst of synthesis of polyurethane foam and polyester synthetic, and RTV silicone rubber.
Ideal applications for Patcat 3020 include solvent-based, chemical cross-linking, two-component polyurethane systems.


Patcat 3020 is used solvent-based, chemical cross-linking, two-component coating.
Patcat 3020 is suitable for polyurethane coatings, inks, adhesives and sealants.
Patcat 3020 is suitable for room temperature vulcanized silica gel, adhesives, and caulking agents.


Patcat 3020 is mainly used in polyurethane rigid foam, spraying, pouring, plate, etc.
Patcat 3020 can be used as heat stabilizer in PVC soft products
Patcat 3020 is suitable for silane cross-linked products.


Patcat 3020 is used as a catalyst for polyurethane production from isocyanates and diols.
Patcat 3020 is used as a catalyst for transesterification and for the room temperature vulcanization of silicones.
Patcat 3020 is used catalyst in the production of polyurethane and curing of room temperature vulcanising silicon rubber.


Patcat 3020 is also used in heat stabilisers in PVC.
Patcat 3020 is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.


Other release to the environment of Patcat 3020 is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).


Release to the environment of Patcat 3020 can occur from industrial use: as processing aid, formulation in materials, in processing aids at industrial sites, in the production of articles and as processing aid.
Patcat 3020 is used in the following products: adhesives and sealants and coating products.


Other release to the environment of Patcat 3020 is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).


Patcat 3020 can be found in complex articles, with no release intended: vehicles, machinery, mechanical appliances and electrical/electronic products (e.g. computers, cameras, lamps, refrigerators, washing machines) and electrical batteries and accumulators.
Patcat 3020 also finds application as catalyst in the manufacture of silane-crosslinking polyolefins.


Patcat 3020 can be found in products with material based on: fabrics, textiles and apparel (e.g. clothing, mattress, curtains or carpets, textile toys), leather (e.g. gloves, shoes, purses, furniture), rubber (e.g. tyres, shoes, toys) and wood (e.g. floors, furniture, toys).
Patcat 3020 is used in the following products: adhesives and sealants, coating products and fillers, putties, plasters, modelling clay.


Patcat 3020 is used in the following areas: building & construction work.
Other release to the environment of Patcat 3020 is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.


Patcat 3020 is used in the following products: polymers, adhesives and sealants, coating products, paper chemicals and dyes, textile treatment products and dyes, metal surface treatment products, non-metal-surface treatment products, polishes and waxes and washing & cleaning products.
Patcat 3020 has an industrial use resulting in manufacture of another substance (use of intermediates).


Release to the environment of Patcat 3020 can occur from industrial use: formulation of mixtures, formulation in materials, in processing aids at industrial sites, in the production of articles, as processing aid and as processing aid.
Patcat 3020 is used in the following areas: building & construction work and formulation of mixtures and/or re-packaging.


Patcat 3020 is used in the following products: polymers, adhesives and sealants, coating products, metal surface treatment products, non-metal-surface treatment products, paper chemicals and dyes, polishes and waxes, textile treatment products and dyes and washing & cleaning products.
Patcat 3020 has an industrial use resulting in manufacture of another substance (use of intermediates).


Patcat 3020 is used for the manufacture of: chemicals, plastic products, electrical, electronic and optical equipment, machinery and vehicles, textile, leather or fur, wood and wood products, pulp, paper and paper products, rubber products, fabricated metal products and furniture.


Release to the environment of Patcat 3020 can occur from industrial use: in the production of articles, as processing aid, in processing aids at industrial sites, as processing aid, formulation in materials and as an intermediate step in further manufacturing of another substance (use of intermediates).


Release to the environment of Patcat 3020 can occur from industrial use: manufacturing of the substance.
Patcat 3020 is used as a paint additive.
Together with dibutyltin dioctanoate, Patcat 3020 is used as a catalyst for polyurethane production from isocyanates and diols.


Patcat 3020 is also useful as a catalyst for transesterification and for the room temperature vulcanization of silicones.
Patcat 3020 is also added to animal feed to remove cecal worms, roundworms, and tapeworms in chickens and turkeys and to prevent or provide treatment against hexamitosis and coccidiosis.


Patcat 3020 is used as a catalyst .
Patcat 3020 is used in the range of 0.1 – 0.5% referring to polyol as primary catalyst for most PUR – formulations and as a secondary catalyst 0.03 – 0.3% recommended.


Patcat 3020 is also used as a stabilizer in polyvinyl chloride, vinyl ester resins, lacquers, and elastomers.
For silicone systems 0.1 – 1% required for hardening.
It is recommended that the appropriate addition level of Patcat 3020 is determined experimentally.


-Patcat 3020 Catalyst for Polyurethane Coating Systems
Patcat 3020 is a catalyst for solvent-based two-component polyurethane systems.
This solution of Patcat 3020 is suitable for accelerating cross-linking processes.



BENEFITS OF PATCAT 3020:
Benefits of Dibutyltin Dilaurate Catalysts for Polyurethane Coatings
*Patcat 3020 improves the drying of chemically curing systems favoring the isocyanate/polyol reaction over other side reactions such as isocyanate/water.
*Patcat 3020 enhances scratch resistance, hardness, and mechanical properties.
*Patcat 3020 can be used to aid the curing process of polyurethanes, silicone resins, RTV silicone resins, and silane modified polymers.



FEATURES OF PATCAT 3020:
*Patcat 3020 is suitable to accelerate the cross-linking process of solvent-based two-component PU coatings
*Patcat 3020 improves the drying of chemically curing systems favoring the isocyanate/polyol reaction over other side reactions such as isocyanate/water
*Patcat 3020 enhances scratch resistance, hardness, and mechanical properties
*Patcat 3020 can be used to aid the curing process of polyurethanes, silicone resins, RTV silicone resins, and silane modified polymers



COMPOUND TYPE OF PATCAT 3020:
*Household Toxin
*Industrial/Workplace Toxin
*Organic Compound
*Organometallic
*Synthetic Compound
*Tin Compound



ALTERNATIVE PARENTS OF PATCAT 3020:
*Straight chain fatty acids
*Monocarboxylic acids and derivatives
*Carboxylic acids
*Organotin compounds
*Organic salts
*Organic oxides
*Hydrocarbon derivatives
*Carbonyl compounds



SUBSTITUENTS OF PATCAT 3020:
*Medium-chain fatty acid
*Straight chain fatty acid
*Monocarboxylic acid or derivatives
*Carboxylic acid
*Carboxylic acid derivative
*Organic oxygen compound
*Organic oxide
*Hydrocarbon derivative
*Organic salt
*Organotin compound
*Organooxygen compound
*Organometallic compound
*Organic post-transition metal moeity
*Carbonyl group
*Aliphatic acyclic compound



CHEMICAL PROPERTIES OF PATCAT 3020:
Patcat 3020 is pale yellow flammable liquid, and soluble in acetone and benzene, can not dissolve in water.
Patcat 3020 has excellent transparency, lubricity and weather resistance.
Patcat 3020 is used in soft and transparent PVC products.
After processing, the surface gloss and transparency of the finished products are good, and there is no vulcanization pollution.


*Organic tin additive
Patcat 3020 is an organic tin additives, and can be soluble in benzene, toluene, carbon tetrachloride, ethyl acetate, chloroform, acetone, petroleum ether and other organic solvents and all industrial plasticizers, but insoluble in water.
Multipurpose high-boiling organic tin catalyst circulation of Patcat 3020 are usually specially treated liquefaction, and at room temperature as a pale yellow or colorless oily liquid, when low temperature as white crystals, and it can be used for PVC additives, it also has excellent lubricity, transparency, weather resistance, and better resistance for sulfide pollution.



PRODUCTION METHOD OF PATCAT 3020:
Patcat 3020 is condensed by DBTO and lauric acid at 60℃.
After condensation, vacuum dehydration, cooling, pressure filtration derived products.



RELATED COMPOUNDS OF PATCAT 3020:
Dibutyltin dioctanoate (CH3(CH2)6CO2)2Sn(CH2CH2CH2CH3)2: CAS#4731-77-5
Dibutyltin diacetate (CH3CO2)2Sn(CH2CH2CH2CH3)2: CAS #1067-33-0



DECOMPOSITION OF PATCAT 3020:
Upon heating to decomposition temperature (which is above 250 °C), Patcat 3020 emits acrid smoke and fumes.



PERFORMANCE OF PATCAT 3020:
Patcat 3020 is a primary catalyst to accelerate the isocyanate-hydroxyl-reaction as well as the reaction of isocyanates with alcohols.
Patcat 3020 can be combined with tertiary amines and calcium-2-ethyl-hexanoate.
Patcat 3020 can also be used for silanol condensation reaction



PHYSICAL and CHEMICAL PROPERTIES of PATCAT 3020:
Tin Content: 18.50 + 0.5%
Appearance: Clear, yellowish liquid
Refractive Index: 1.4610 + 0.005 (25°C)
Specific Gravity (approx.): 1.040 (g/cm³ @ 25°C)
Colour: 4 max (Gardner)
Viscosity: < 75 cP (@ 25°C)
Flash Point: >150°C (PMCC)
Solidification Point: ≤ -3°C
Chemical Formula: (CH3(CH2)10CO2)2Sn((CH2)3CH3)2
Molar Mass: 631.570 g·mol−1

Appearance: Colourless oily liquid or soft waxy crystals
Odor: Fatty
Density: 1.066 g/cm3
Melting Point: 22 to 24 °C (72 to 75 °F; 295 to 297 K)
Boiling Point: 205 °C at 1.3 kPa
Solubility in Water: Practically insoluble (0.00143 g/l at 68 °F (20 °C))
Solubility: Practically insoluble in methanol, soluble in petroleum ether,
benzene, acetone, ether, carbon tetrachloride, organic esters
Vapor Pressure: Refractive Index (nD): 1.4683 at 20 °C (for light at wavelength of 589.29 nm)
Viscosity: 42 cP

Chemical formula: (CH3(CH2)10CO2)Sn((CH2)3CH3)2
Molar mass: 631.570 g·mol−1
Appearance: Colourless oily liquid or soft waxy crystals
Odor: Fatty
Density: 1.066 g/cm3
Melting point: 22 to 24 °C (72 to 75 °F; 295 to 297 K)
Boiling point: 205 °C at 1.3 kPa
Solubility in water: Practically insoluble (less than 1 mg/mL at 68 °F (20 °C))
Solubility: Practically insoluble in methanol
Soluble in: petroleum ether, benzene, acetone, ether,
carbon tetrachloride, organic esters
Vapor pressure:
Refractive index (nD): 1.4683 at 20 °C (for light at wavelength of 589.29 nm)
Viscosity: 42 cP
Appearance: colorless to yellow liquid
Tin content: 17.0~19.0%
Density at 25℃: 1.06g/ml
Boiling point at 12mmHg: >205℃
Flash point, Tag closed cup: 113℃
Refractive index (25℃): 1.471
Compound Formula: C32H64O4Sn
Molecular Weight: 631.56
Appearance: Yellow liquid

Melting Point: 22-24 °C
Boiling Point: 205 °C
Density: 1.066 g/mL
Solubility in H2O: N/A
Exact Mass: 632.382655
Monoisotopic Mass: 632.382655
Molecular Weight: 631.6
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 30
Exact Mass: 632.382663
Monoisotopic Mass: 632.382663
Topological Polar Surface Area: 52.6 Ų

Heavy Atom Count: 37
Formal Charge: 0
Complexity: 477
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Appearance: yellow liquid to paste (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity: 1.06600 @ 25.00 °C.
Refractive Index: 1.47100 @ 20.00 °C.
Melting Point: 23.00 °C. @ 760.00 mm Hg
Boiling Point: 560.00 to 561.00 °C. @ 760.00 mm Hg (est)
Flash Point: > 230.00 °F. TCC ( > 110.00 °C. )
logP (o/w): 3.120
Soluble in: water, 3 mg/L @ 25 °C (est)

Physical state: solid
Color: colorless, to, light yellow
Odor: fatty odor
Melting point: 28,5 °C
Initial boiling point and boiling range: 205 °C at 130 hPa - (ECHA)
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: 189 - 193 °C - closed cup
Autoignition temperature: No data available
Decomposition temperature: > 250 °C -
pH: No data available
Viscosity Viscosity, kinematic: No data available
Viscosity, dynamic: No data available

Water solubility 0,00143 g/l at 20 °C
Partition coefficient: n-octanol/water Pow: 27.700; log Pow: 4,44 at 21 °C
Vapor pressure: < 0,01 hPa at 25 °C
Density: 1,066 g/cm3 at 25 °C - lit.
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: none
Other safety information: No data available

Appearance: Yellowish oily liquid
Tin Content: 18.2
Density: 1.05±0.02
Refractive Index: 1.468±0.001
Boiling Point: >204℃/12mm
Melting Point: 22-24℃
Freezing Point: ≤8℃
Flash Point: >230℃
Volatile: ≤0.4%

Boiling point: >250 °C (1013 hPa)
Density: 1.05 g/cm3 (20 °C)
Flash point: 191 °C
Ignition temperature: >200 °C
Melting Point: 25 - 27 °C
Vapor pressure: Solubility: Formula: (C4H9)2Sn(OOC(CH2)10CH3)2 / C32H64O4Sn
Molecular mass: 631.6
Boiling point at 1.3kPa: 205°C
Melting point: 22-24°C
Vapour pressure: negligible

Solubility in water: none
Flash point: 191°C
Density (at 20°C): 1.05 g/cm³
Octanol/water partition coefficient as log Pow: 4.44
Density: 1.066 g/mL at 25 °C(lit.)
Boiling Point: 560.5±19.0 °C at 760 mmHg
Melting Point: 22-24°C
Molecular Formula: C32H64O4Sn
Molecular Weight: 631.558
Flash Point: 292.8±21.5 °C
Exact Mass: 632.382690
PSA: 52.60000
LogP: 17.44

Vapour Pressure: 0.0±1.5 mmHg at 25°C
Index of Refraction: n20/D 1.471(lit.)
Stability: Stability Combustible.
Incompatible with strong oxidizing agents.
Water Solubility: Freezing Point: 8℃
Compound Formula: C32H64O4Sn
Molecular Weight: 631.56 g/mol
Appearance: Yellow liquid
Melting Point: 22-24 °C
Boiling Point: 205 °C
Density: 1.066 g/mL
Solubility in H2O: Not Applicable
Exact Mass: 632.382655 g/mol
Monoisotopic Mass: 632.382655 g/mol



FIRST AID MEASURES of PATCAT 3020:
-After inhalation:
Fresh air.
Immediately call in physician.
-In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Call a physician immediately.
-After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
-After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of PATCAT 3020:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Take up carefully.
Dispose of properly.



FIRE FIGHTING MEASURES of PATCAT 3020:
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of PATCAT 3020:
-Control parameters:
*Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses.
*Skin protection:
Full contact:
Material: Chloroprene
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 30 min
*Body Protection:
protective clothing
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of PATCAT 3020:
-Precautions for safe handling:
*Advice on safe handling:
Work under hood.
*Hygiene measures:
Immediately change contaminated clothing.
Wash hands and face after working with substance.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
Keep in a well-ventilated place.
Keep locked up or in an area accessible only to qualified or authorized persons.



STABILITY and REACTIVITY of PATCAT 3020:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .


Patent Blue
2-PHOSPHONOBUTANE-1,2,4-TRICARBOXYLIC ACID; PBTC; Bayhibit AM; PBS-AM; Phosphonobutanetricarboxylic acid; 2-Phosphono-1,2,4-butanecarboxylic acid; CAS NO: 37971-36-1
P-BENZOQUINONE
P-BENZOQUINONE


CAS Number: 106-51-4
EC Number: 203-405-2
MDL number: MFCD00001591
Chemical formula: C6H4O2


p-benzoquinone, commonly known as para-quinone, is a chemical compound with the formula C6H4O2.
In a pure state, p-benzoquinone forms bright-yellow crystals with a characteristic irritating odor, resembling that of chlorine, bleach, and hot plastic or formaldehyde.
This six-membered ring compound is the oxidized derivative of p-benzoquinone.


The molecule is multifunctional: p-benzoquinone exhibits properties of a ketone, being able to form oximes; an oxidant, forming the dihydroxy derivative; and an alkene, undergoing addition reactions, especially those typical for α,β-unsaturated ketones.
p-benzoquinone is sensitive toward both strong mineral acids and alkali, which cause condensation and decomposition of the compound.
p-benzoquinone is a yellow, crystalline material or large yellow, monoclinic prisms.


p-benzoquinone is the chemical compound with the formula C6H4O2.
This nonaromatic six-membered ring compound is the oxidized derivative of p-benzoquinone.
p-benzoquinone is multifunctional: p-benzoquinone exhibits properties of a ketone, forming an oxime; an oxidant, forming the dihydroxy derivative; and an alkene, undergoing addition reactions.


p-Benzoquinone is a yellow, crystalline (sand-like) solid with a Chlorine-like odor.
p-benzoquinone was first produced commercially in 1919, and has since been manufactured in several European countries, Japan and the United States.
p-Benzoquinone is the simplest member of the class of 1,4-benzoquinones, obtained by the formal oxidation of hydroquinone to the corresponding diketone.


p-Benzoquinone is a metabolite of benzene.
p-Benzoquinone is a natural product found in Blaps lethifera, Euglena gracilis, and other organisms with data available.
p-Benzoquinone appears as a yellowish-colored crystalline solid with a pungent, irritating odor.
p-benzoquinone is yellow crystal.


p-benzoquinone's melting point is 116 ° C and the relative density is 1.318 (20 / 4 ° C).
p-benzoquinone is soluble in ethanol, ether and alkali, slightly soluble in water.
p-benzoquinone sublimates and the vapor is volatile and partially decomposes.
p-benzoquinone has a pungent odor similar to chlorine.


p-benzoquinone is dissolved in ethanol, and slightly dissolved in acetone, but insoluble in water, benzene and gasoline.
p-Benzoquinone is soluble in water and denser than water.
If moist p-Benzoquinone may decompose spontaneously above 140°F.
This has occurred in drums, causing over-pressurization.


p-Benzoquinone acts as an oxidizing agent.
p-benzoquinone, also known as benzoquinone or 1,4-benzochinon, belongs to the class of organic compounds known as p-benzoquinones.
These are benzoquinones where the two C=O groups are attached at the 1- and 4-positions, respectively.
p-benzoquinoneis an extremely weak basic (essentially neutral) compound (based on its pKa).


p-benzoquinoneexists in all living species, ranging from bacteria to humans.
p-benzoquinonehas been detected, but not quantified in, a few different foods, such as anises, barley, and olives.
This could make p-benzoquinone a potential biomarker for the consumption of these foods.
p-benzoquinone exists as a large yellow, monoclinic prism with an irritating odour resembling that of chlorine.


p-benzoquinonewas first produced commercially in 1919 and has since been manufactured in several European countries.
p-benzoquinone appears as a yellowish-colored crystalline solid with a pungent, irritating odor.
p-benzoquinone, commonly known as para-quinone, is a chemical compound with the formula C6H4O2.
p-benzoquinone is the basic structure of quinonoid compounds.


They are widely distributed in the natural world, being found in bacteria, plants and arthropods and hence quinones are ubiquitous to living systems.
Quinones play pivotal role in biological functions including oxidative phosphorylation and electron transfer.
p-benzoquinone is the simplest member of the class of 1,4-benzoquinones, obtained by the formal oxidation of hydroquinone to the corresponding diketone.


p-benzoquinone is a metabolite of benzene.
p-benzoquinone is Light yellow crystals with an acrid odor resembling chlorine.
p-benzoquinone's odor threshold concentration is 84 ppb.
p-benzoquinone exists as a large yellow, monoclinic prism with an irritating odour resembling that of chlorine.


p-benzoquinone was first produced commercially in 1919 and has since been manufactured in several European countries.
When heated to near its melting point, p-benzoquinone sublimes, even at atmospheric pressure, allowing for an effective purification.
Impure samples are often dark-colored due to the presence of quinhydrone, a dark green 1:1 charge-transfer complex of quinone with hydroquinone.



USES and APPLICATIONS of P-BENZOQUINONE:
1,4-Benzoquinone is used in the synthesis of Bromadol and related analogs.
p-benzoquinone's major use is in hydroquinone production, but it is also used as a polymerisation inhibitor and as an intermediate in the production of a variety of substances, including rubber accelerators and oxidising agents.
p-benzoquinone is used in the dye, textile, chemical, tanning, and cosmetic industries.


In chemical synthesis for p-benzoquinone and other chemicals, quinone is used as an intermediate.
p-benzoquinone is also used in the manufacturing industries and chemical laboratory associated with protein fibre, photographic film, hydrogen peroxide, and gelatin making.
p-benzoquinone is extensively used as a chemical intermediate, a polymerisation inhibitor, an oxidising agent, a photographic chemical, a tanning agent, and a chemical reagent.


p-benzoquinone is used as a chemical intermediate, a polymerization inhibitor, an oxidizing agent, a photographic chemical, a tanning agent, and a chemical reagent.
p-benzoquinone's major use is in hydroquinone production, but it is also used as a polymerization inhibitor and as an intermediate in the production of a variety of substances, including rubber accelerators and oxidizing agents


p-Benzoquinone is widely used in medicine, pesticides, chemicals, dyes, etc.
p-benzoquinone is used as a fungicide, as a reagent in
photography, and to make dyes and other chemicals.
p-Benzoquinone is used as a catalyst in the preperation of allyl silyl ethers.


p-Benzoquinone is a superoxide scavenger that has been used in the characterization of carnation-like SnS2 nanostructure photocatalysts for photodegredation.
Oxidation of p-benzoquinone is facile.
One such method makes use of hydrogen peroxide as the oxidizer and iodine or an iodine salt as a catalyst for the oxidation occurring in a polar solvent; e.g. isopropyl alcohol.


p-Benzoquinone is used as a dienophile in Diels-Alder cycloadditions to prepare naphthoquinones and 1,4-phenanthrenediones.
p-benzoquinone acts as a dehydrogenation reagent and an oxidizer in synthetic organic chemistry.
In the Thiele-Winter reaction, p-benzoquinone is involved in the preparation of triacetate of hydroxyquinol by reacting with acetic anhydride and sulfuric acid.
p-benzoquinone is also used in the synthesis of bromadol and to suppress double- bond migration during olefin metathesis reactions.


p-benzoquinone is used as a precursor to hydroquinone which finds application in photography and as a reducing agent and an antioxidant in rubber production.
p-benzoquinone is used intermediates for dyes and pharmaceuticals.
p-benzoquinone is used as a qualitative test for celery, pyridine, azole, tyrosine and hydroquinone.


p-benzoquinone is used for the determination of amino acids in the analysis.
p-Benzoquinone is used to make dyes and as a photographic chemical.
p-Benzoquinone is used as a dienophile in Diels-Alder cycloadditions to prepare naphthoquinones and 1,4-phenanthrenediones.
p-benzoquinone acts as a dehydrogenation reagent and an oxidizer in synthetic organic chemistry.


In the Thiele-Winter reaction, p-benzoquinone is involved in the preparation of triacetate of hydroxyquinol by reacting with acetic anhydride and sulfuric acid.
p-benzoquinone is also used in the synthesis of bromadol and to suppress double- bond migration during olefin metathesis reactions.
p-benzoquinone is used as a precursor to hydroquinone which finds application in photography and as a reducing agent and an antioxidant in rubber production.


p-Benzoquinone, also known as para-quinone or 1,4-Benzoquinone, is used as a precursor to hydroquinone.
p-benzoquinone, 99% Cas 106-51-4 - used in the synthesis of bromadol and to suppress double- bond migration during olefin metathesis reactions.
p-benzoquinone, 99% Cas 106-51-4 - used as a precursor to hydroquinone which finds application in photography and as a reducing agent and an antioxidant in rubber production.


p-benzoquinone is extensively used as a chemical intermediate, a polymerisation inhibitor, an oxidising agent, a photographic chemical, a tanning agent, and a chemical reagent.
p-benzoquinone's major use is in hydroquinone production, but it is also used as a polymerisation inhibitor and as an intermediate in the production of a variety of substances, including rubber accelerators and oxidising agents.


p-benzoquinone is used in the dye, textile, chemical, tanning, and cosmetic industries.
In chemical synthesis for hydroquinone and other chemicals, p-benzoquinone is used as an intermediate.
p-benzoquinone is also used in the manufacturing industries and chemical laboratory associated with protein fibre, photographic film, hydrogen peroxide, and gelatin making.


p-benzoquinone is used in the manufacture of dyes, fungicide, and hydroquinone; for tanning hides; as an oxidizing agent; in photography; making gelatin insoluble; strengthening animal fibers and as reagent.
p-benzoquinone is a dehydrogenation reagent.
The derivatives tetrachloro-1,4-benzoquinone and 2,3-dichloro-5,6-dicyanobenzoquinone are stronger oxidants.
Whereas the resulting phenolate as reaction product of 1,4-benzoquinone (hydroquinone) is nucleophilic, a similar oxidant - 3,3',5'5-tetra-tert-butyldiphenoquinone - can be used in the presence of sensitive electrophilic groups.


-Applications of p-benzoquinone in organic synthesis:
p-benzoquinone is used as a hydrogen acceptor and oxidant in organic synthesis.
p-benzoquinone serves as a dehydrogenation reagent.
p-benzoquinone is also uses as a dienophile in Diels Alder reactions.



PREPARATION OF P-BENZOQUINONE:
p-benzoquinone is prepared industrially by oxidation of hydroquinone, which can be obtained by several routes.
One route involves oxidation of diisopropylbenzene and the Hock rearrangement.
The net reaction can be represented as follows:

C6H4(CHMe2)2 + 3 O2 → C6H4O2 + 2 OCMe2 + H2O
The reaction proceeds via the bis(hydroperoxide) and the hydroquinone.
Acetone is a coproduct.

Another major process involves the direct hydroxylation of phenol by acidic hydrogen peroxide: C6H5OH + H2O2 → C6H4(OH)2 + H2O
Both hydroquinone and catechol are produced.
Subsequent oxidation of the hydroquinone gives the quinone.
p-benzoquinone was originally prepared industrially by oxidation of aniline, for example by manganese dioxide.
This method is mainly practiced in PRC where environmental regulations are more relaxed.



STRUCTURE AND REDOX OF P-BENZOQUINONE:
p-benzoquinone is a planar molecule with localized, alternating C=C, C=O, and C–C bonds.
Reduction gives the semiquinone anion C6H4O2−}, which adopts a more delocalized structure.
Further reduction coupled to protonation gives the hydroquinone, wherein the C6 ring is fully delocalized.





REACTIONS AND APPLICATIONS OF P-BENZOQUINONE:
p-benzoquinone is mainly used as a precursor to hydroquinone, which is used in photography and rubber manufacture as a reducing agent and antioxidant.
Benzoquinonium is a skeletal muscle relaxant, ganglion blocking agent that is made from p-benzoquinone.
p-Benzoquinone and its derivatives are extensively used in Diels-Alder reactions.
A facile tautomerization of alkyl substituted p-Benzoquinone to o-quinone methide is the highlight of this cycloaddition.



ORGANIC SYNTHESIS OF P-BENZOQUINONE:
p-benzoquinone is used as a hydrogen acceptor and oxidant in organic synthesis.
p-benzoquinone serves as a dehydrogenation reagent.
p-benzoquinone is also used as a dienophile in Diels Alder reactions.
Benzoquinone reacts with acetic anhydride and sulfuric acid to give the triacetate of hydroxyquinol.
This reaction is called the Thiele reaction or Thiele–Winter reaction after Johannes Thiele, who first described it in 1898, and after Ernst Winter, who further described p-benzoquinone's reaction mechanism in 1900.

p-benzoquinone is also used to suppress double-bond migration during olefin metathesis reactions.
An acidic potassium iodide solution reduces a solution of benzoquinone to hydroquinone, which can be reoxidized back to the quinone with a solution of silver nitrate.
Due to its ability to function as an oxidizer, 1,4-benzoquinone can be found in methods using the Wacker-Tsuji oxidation, wherein a palladium salt catalyzes the conversion of an alkene to a ketone.
This reaction is typically carried out using pressurized oxygen as the oxidizer, but benzoquinone can sometimes preferred.
p-benzoquinone is also used as a reagent in some variants on Wacker oxidations.



PRODUCTION METHODS OF P-BENZOQUINONE:
p-benzoquinone was produced as early as 1838 by oxidation of quinic acid with manganese dioxide.
p-benzoquinone can be prepared by oxidation starting with aniline or by the oxidation of hydroquinone with bromic acid.
More recently, p-benzoquinone has been made biosynthetically from D-glucose.



METABOLISM OF P-BENZOQUINONE:
1,4-Benzoquinone is a toxic metabolite found in human blood and can be used to track exposure to benzene or mixtures containing benzene and benzene compounds, such as petrol.
p-benzoquinone is excreted in its original form and also as variations of its own metabolite, hydroquinone.



ALTERNATIVE PARENTS OF P-BENZOQUINONE:
*Organic oxides
*Hydrocarbon derivatives



SUBSTITUENTS OF P-BENZOQUINONE:
*P-benzoquinone
*Organic oxide
*Hydrocarbon derivative
*Aliphatic homomonocyclic compound



PHYSICAL and CHEMICAL PROPERTIES of P-BENZOQUINONE:
Molar mass: 108.096 g·mol−1
Appearance: Yellow solid
Odor: Acrid, chlorine-like[2]
Density: 1.318 g/cm3 at 20 °C
Melting point: 115 °C (239 °F; 388 K)
Boiling point: Sublimes
Solubility in water: 11 g/L (18 °C)
Solubility: Slightly soluble in petroleum ether; soluble in acetone; 10% in ethanol, benzene, diethyl ether
Vapor pressure: 0.1 mmHg (25 °C)
Magnetic susceptibility (χ): -38.4·10−6 cm3/mol
Molecular Weight: 108.09
XLogP3: 0.2

Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 0
Exact Mass: 108.021129366
Monoisotopic Mass: 108.021129366
Topological Polar Surface Area: 34.1 Ų
Heavy Atom Count: 8
Formal Charge: 0
Complexity: 149
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Appearance: yellow crystalline solid (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in: ater, 1.11E+04 mg/L @ 18C (exp)
Physical state: Solid.
Form: Crystalline powder.
Color: Yellow. Green.
Odor: Pungent odor.
Odor threshold: 0.08 ppm
pH: Not available.
Melting point/freezing point: 240.26 °F (115.7 °C)
Initial boiling point and boiling range: Not available.

Flash point: Not available.
Evaporation rate: Not available.
Flammability (solid, gas): Not available.
Upper/lower flammability or explosive limits:
Flammability limit - lower (%): Not available.
Flammability limit - upper (%): Not available.
Explosive limit - lower (%): Not available.
Explosive limit - upper (%): Not available.
Vapor pressure: 0.01 kPa at 25 °C
Vapor density: 3.7
Relative density: Not available.
Solubility(ies):
Solubility (water): Slightly soluble.

Partition coefficient: (n-octanol/water): 0.2
Auto-ignition temperature: 1040 °F (560 °C)
Decomposition temperature: Not available.
Viscosity: Not available.
Other information:
Molecular formula: C6-H4-O2
Molecular weight: 108.09 g/mol
Specific gravity: 1.32 at 20 °C
Surface tension: 32.58 mN/m
Appearance and properties: yellow to green crystalline solid
Density: 1.31
Boiling point: 293°C
Melting point: 113-115 °C(lit.)
Flash point: 38°C
Refractive index: n20/D 1.453
Water solubility: 10 g/L (25 ºC)

Melting point: 113-115 °C(lit.)
Boiling point: 293°C
Density: 1.31
vapor density: 3.73 (vs air)
vapor pressure: 0.1 mm Hg ( 25 °C)
refractive index: n20/D 1.453
Flash point: 38°C
storage temp.: room temp
solubility: 10g/l
form: Powder
pka: 7.7
color: Yellow to green
PH: 4 (1g/l, H2O, 20℃)
Water Solubility: 10 g/L (25 ºC)

Water Solubility: 45.4 g/L
logP: 0.21
logP: 1.02
logS: -0.38
pKa (Strongest Basic): -7.7
Physiological Charge: 0
Hydrogen Acceptor Count: 2
Hydrogen Donor Count: 0
Polar Surface Area: 34.14 Ų
Rotatable Bond Count: 0
Refractivity: 31.03 m³·mol⁻¹
Polarizability: 9.75 ų
Number of Rings: 1
Bioavailability: Yes
Rule of Five: Yes
Ghose Filter: No
Veber's Rule: Yes
MDDR-like Rule: No



FIRST AID MEASURES of P-BENZOQUINONE:
-Description of first aid measures:
*General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
*If inhaled:
If breathed in, move person into fresh air.
Consult a physician.
*In case of skin contact:
Wash off with soap and plenty of water.
Take victim immediately to hospital.
Consult a physician.
*In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician
*If swallowed:
Rinse mouth with water.
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of P-BENZOQUINONE:
-Environmental precautions
Do not let product enter drains.
-Methods and materials for containment and cleaning up
Sweep up and shovel.
Keep in suitable, closed containers for disposal.



FIRE FIGHTING MEASURES of P-BENZOQUINONE:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available



EXPOSURE CONTROLS/PERSONAL PROTECTION of P-BENZOQUINONE:
-Exposure controls:
*Appropriate engineering controls:
Wash hands before breaks and immediately after handling the product.
-Personal protective equipment:
*Eye/face protection:
Use face shield and safety glasses.
*Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Wash and dry hands.
-Control of environmental exposure:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.



HANDLING and STORAGE of P-BENZOQUINONE:
-Conditions for safe storage, including any incompatibilities:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.
Storage class (TRGS 510): Non-combustible



STABILITY and REACTIVITY of P-BENZOQUINONE:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available
-Other decomposition products :
No data available



SYNONYMS:
p-Benzoquinone
p-Quinone
1,4-Benzoquinone
1,4-Cyclohexadiene-3,6-dione
p-benzoquinone
1,4-BENZOQUINONE
Benzoquinone
Quinone
106-51-4
p-Quinone
para-Benzoquinone
cyclohexa-2,5-diene-1,4-dione
Chinone
2,5-Cyclohexadiene-1,4-dione
para-Quinone
Cyclohexadienedione
1,4-Benzoquine
1,4-Cyclohexadienedione
1,4-Dioxybenzene
Steara pbq
p-Chinon
Benzo-chinon
Benzo-1,4-quinone
1,4-Diossibenzene
Chinon
1,4-Dioxy-benzol
1,4-Cyclohexadiene dioxide
Semiquinone anion
semiquinone radicals
RCRA waste number U197
NCI-C55845
USAF P-220
Cyclohexadiene-1,4-dione
1,4-Benzochinon
NSC 36324
[1,4]benzoquinone
CHEBI:16509
Quinone1,4-Benzoquinone
MFCD00001591
NSC-36324
CHEMBL8320
3T006GV98U
2,5-Cyclohexadiene-1,4-dione, homopolymer
DSSTox_CID_145
1,4-Benzoquinone, 99%
DSSTox_RID_75398
DSSTox_GSID_20145
Caswell No. 719C
1,4 benzoquinone
26745-90-4
CAS-106-51-4
CCRIS 933
HSDB 1111
EINECS 203-405-2
UN2587
parabenzochinon
UNII-3T006GV98U
p-benzo-quinone
AI3-09068
Quinone
p-BQ
NSC36324
2,4-dione
p-BQ
Benzo-1,4-quinone
QUINONE
(p-Phenylenedioxy)radical
Lopac-B-1266
QUINONE
Benzoquinone
Epitope ID:116219
WLN: L6V DVJ
EC 203-405-2
cid_4650
PARA-QUINONE
Lopac0_000120
SCHEMBL18103
Benzil-related compound, 53
MLS002454445
GTPL6307
2,5-cyclohexadiene-1-4-dione
DTXSID6020145
BDBM22774
1,4-BENZOQUINONE
HMS2230N13
HMS3260G22
ZINC895247
AMY21949
1,4-BENZOQUINONE
Tox21_202020
Tox21_302970
Tox21_500120
BBL010327
Benzoquinone
c0261
STK398389
AKOS000119965
3,6-Dioxo-1,4-cyclohexadiene-1-ide
CCG-204215
LP00120
SDCCGSBI-0050108.P002
UN 2587
p-Benzoquinone, reagent grade, >=98%
NCGC00015139-01
NCGC00015139-02
NCGC00015139-03
NCGC00015139-04
NCGC00015139-05
NCGC00015139-06
NCGC00015139-07
NCGC00015139-10
NCGC00091053-01
NCGC00091053-02
NCGC00091053-03
NCGC00256505-01
NCGC00259569-01
NCGC00260805-01
SMR000326659
VS-02448
DS-000613
B0089
B0887
EU-0100120
B 1266
C00472
2,5-Cyclohexadiene-1,4-dione, radical ion(1-)
A801452
Q402719
SR-01000075705
J-503966
SR-01000075705-1
cyclohexa-2,5-diene-1,4-dione
1,4-Benzoquinone
p-benzoquinone
benzoquinone
quinone
1,4-benzoquinone
p-quinone
chinone
2,5-cyclohexadiene-1,4-dione
cyclohexadienedione
para-quinone, 1,4-benzoquine
Benzoquinone
2,5-Cyclohexadiene-1,4-dione
p-benozquinone
Thiophene,5-dibromo
2,5-dibromo thiophene
cyclohexadiene-1,4-dione
para-benzoquinone
p-Benzoquinone
2,5-dibromothiphene
2,5-bromothiophene
1,3-dibromothiophene
p-Benzoquinone,Quinone
2,5-dibromothiophen
1,4-benzo-quinone
1,4-Benzoquinone
Thiophene,2,5-dibromo
1,4-Benzoquinone
1,4-Cyclohexadienedione
1,4-Dione-2,5-cyclohexadiene
Chinone
NSC 36324
PBQ 2
Quinone
Stearer PBQ
p-Quinone
BENZOQUINONE
P-BENZOQUINONE
QUINONE
PARA BENZOQUINONE
CHINONE
para-quinone
p-Benzochinon
1,4-Benzochinon
2,5-CYCLOHEXADIENE-1,4-DIONE
Cyclohexa-2,5-diene-1,4-dione
1,4-BENZOCHINONE
1,4-BENZOQUINONE
2,5-CYCLOHEXADIENE-1,4-DIONE
BENZOQUINONE
BENZOQUINONE
1,4-, CHINONE
CYCLOHEXADIENEDIONE
PARA BENZOQUINONE
P-BENZOQUINONE
p-benzoquinone 98+ % (dried)
P-QUINONE, QUINONE
1,4-Benzochinon
1,4-Benzoquine
1,4-Cyclohexadiene dioxide
1,4-Cyclohexadienedione
1,4-cyclohexadienedioxide
1,4-Diossibenzene
1,4-dioxybenzene
1,4-Dioxy-benzol
1,4-Benzochinon
1,4-Benzoquine
1,4-Benzoquinone
1,4-Cyclohexadiene dioxide
1,4-Cyclohexadienedione
1,4-Diossibenzene
1,4-Dioxy-benzol
1,4-Dioxybenzene
2,5-Cyclohexadiene-1,4-dione
2,5-Cyclohexadiene-1-4-dione
P-BENZOQUINONE
DESCRIPTION:

P-Benzoquinone, para-quinone, is a chemical compound with the formula C6H4O2.
In a pure state, P-Benzoquinone forms bright-yellow crystals with a characteristic irritating odor, resembling that of chlorine, bleach, and hot plastic or formaldehyde.
This six-membered ring compound is the oxidized derivative of 1,4-hydroquinone.


CAS Number :106-51-4
EC Number :203-405-2
Linear Formula: C6H4(=O)2

SYNONYM(S) OF P-BENZOQUINONE:
Quinone, 1,4-Benzoquinone[1];Benzoquinone;p-Benzoquinone;p-Quinone


The molecule is multifunctional: P-Benzoquinone exhibits properties of a ketone, being able to form oximes; an oxidant, forming the dihydroxy derivative; and an alkene, undergoing addition reactions, especially those typical for α,β-unsaturated ketones.
P-Benzoquinone is sensitive toward both strong mineral acids and alkali, which cause condensation and decomposition of the compound.


P-Benzoquinone is used as a dienophile in Diels-Alder cycloadditions to prepare naphthoquinones and 1,4-phenanthrenediones.
P-Benzoquinone acts as a dehydrogenation reagent and an oxidizer in synthetic organic chemistry.
In the Thiele-Winter reaction, it is involved in the preparation of triacetate of hydroxyquinol by reacting with acetic anhydride and sulfuric acid.

P-Benzoquinone is also used in the synthesis of bromadol and to suppress double- bond migration during olefin metathesis reactions.
P-Benzoquinone is used as a precursor to hydroquinone which finds application in photography and as a reducing agent and an antioxidant in rubber production.


p-Benzoquinone (PBQ) is a cyclic conjugated diketone.
Its high-resolution photoelectron spectrum has been reported.
The visible and near ultraviolet spectra of PBQ have been recorded and analyzed.

Its addition as coagent has been reported to enhance the crosslinking rate of polypropylene initiated by the pyrolysis of peroxides.
Its impact on hemoglobin (Hb) has been investigated based on immunoblots and mass spectral analysis of a smoker′s blood.


PREPARATION OF P-BENZOQUINONE:
1,4-Benzoquinone is prepared industrially by oxidation of hydroquinone, which can be obtained by several routes.
One route involves oxidation of diisopropylbenzene and the Hock rearrangement.
The net reaction can be represented as follows:
C6H4(CHMe2)2 + 3 O2 → C6H4O2 + 2 OCMe2 + H2O

The reaction proceeds via the bis(hydroperoxide) and the hydroquinone.
Acetone is a coproduct.
Another major process involves the direct hydroxylation of phenol by acidic hydrogen peroxide: C6H5OH + H2O2 → C6H4(OH)2 + H2O Both hydroquinone and catechol are produced.

Subsequent oxidation of the hydroquinone gives the quinone.[8]
Quinone was originally prepared industrially by oxidation of aniline, for example by manganese dioxide.
This method is mainly practiced in PRC where environmental regulations are more relaxed.

Oxidation of hydroquinone is facile.
One such method makes use of hydrogen peroxide as the oxidizer and iodine or an iodine salt as a catalyst for the oxidation occurring in a polar solvent; e.g. isopropyl alcohol.
When heated to near its melting point, 1,4-benzoquinone sublimes, even at atmospheric pressure, allowing for an effective purification.
Impure samples are often dark-colored due to the presence of quinhydrone, a dark green 1:1 charge-transfer complex of quinone with hydroquinone.

STRUCTURE AND REDOX OF P-BENZOQUINONE:
C–C and C–O bond distances in benzoquinone (Q), its 1e reduced derivative (Q−), and hydroquinone (H2Q).
Benzoquinone is a planar molecule with localized, alternating C=C, C=O, and C–C bonds.
Reduction gives the semiquinone anion C6H4O2−}, which adopts a more delocalized structure.
Further reduction coupled to protonation gives the hydroquinone, wherein the C6 ring is fully delocalized.


REACTIONS AND APPLICATIONS OF P-BENZOQUINONE:
Quinone is mainly used as a precursor to hydroquinone, which is used in photography and rubber manufacture as a reducing agent and antioxidant.
Benzoquinonium is a skeletal muscle relaxant, ganglion blocking agent that is made from benzoquinone.


ORGANIC SYNTHESIS OF P-BENZOQUINONE:
P-Benzoquinone is used as a hydrogen acceptor and oxidant in organic synthesis.
1,4-Benzoquinone serves as a dehydrogenation reagent.
P-Benzoquinone is also used as a dienophile in Diels Alder reactions.


Benzoquinone reacts with acetic anhydride and sulfuric acid to give the triacetate of hydroxyquinol.
This reaction is called the Thiele reaction or Thiele–Winter reaction[19][20] after Johannes Thiele, who first described it in 1898, and after Ernst Winter, who further described its reaction mechanism in 1900.

An application is found in this step of the total synthesis of Metachromin A:
Benzoquinone is also used to suppress double-bond migration during olefin metathesis reactions.
An acidic potassium iodide solution reduces a solution of benzoquinone to hydroquinone, which can be reoxidized back to the quinone with a solution of silver nitrate.
Due to its ability to function as an oxidizer, 1,4-benzoquinone can be found in methods using the Wacker-Tsuji oxidation, wherein a palladium salt catalyzes the conversion of an alkene to a ketone.

This reaction is typically carried out using pressurized oxygen as the oxidizer, but benzoquinone can sometimes preferred.
P-Benzoquinone is also used as a reagent in some variants on Wacker oxidations.
1,4-Benzoquinone is used in the synthesis of Bromadol and related analogs.


2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) is a stronger oxidant and dehydrogenation agent than 1,4-benzoquinone.
Chloranil 1,4-C6Cl4O2 is another potent oxidant and dehydrogenation agent.
Monochloro-p-benzoquinone is yet another but milder oxidant.


METABOLISM OF P-BENZOQUINONE:
1,4-Benzoquinone is a toxic metabolite found in human blood and can be used to track exposure to benzene or mixtures containing benzene and benzene compounds, such as petrol.
The compound can interfere with cellular respiration, and kidney damage has been found in animals receiving severe exposure.
It is excreted in its original form and also as variations of its own metabolite, hydroquinone.


APPLICATIONS OF P-BENZOQUINONE:
p-Benzoquinone may be used to form benzofuranone derivatives on reacting with anilides of β-aminocrotonic acids via Nenitzescu reaction.
Dienophile employed in Diels-Alder cycloadditions to form naphthoquinones,[6] and 1,4-phenanthrenediones.

Oxidant used in first step of greener amine synthesis from terminal olefins by Wacker oxidation followed by transfer hydrogenation of the resultant imine.




p-Benzoquinone is used as a dienophile in Diels-Alder cycloadditions to prepare naphthoquinones and 1,4phenanthrenediones.
P-Benzoquinone acts as a dehydrogenation reagent and as an oxidant in synthetic organic chemistry.

In the Thiéle-Winter reaction, it is involved in the preparation of hydroxyquinol triacetate by reacting with acetic anhydride and sulfuric acid.
P-Benzoquinone is also used in the synthesis of bromadol and to suppress the migration of double bonds during olefin metathesis reactions.
P-Benzoquinone is used as a precursor of hydroquinone which finds its application in photography and as a reducing agent and antioxidant in the production of rubber.




CHEMICAL AND PHYSICAL PROPERTIES OF P-BENZOQUINONE:
Chemical formula C6H4O2
Molar mass 108.096 g•mol−1
Appearance Yellow solid
Odor Acrid, chlorine-like[2]
Density 1.318 g/cm3 at 20 °C
Melting point 115 °C (239 °F; 388 K)
Boiling point Sublimes
Solubility in water 11 g/L (18 °C)
Solubility Slightly soluble in petroleum ether; soluble in acetone; 10% in ethanol, benzene, diethyl ether
Vapor pressure 0.1 mmHg (25 °C)[2]
Magnetic susceptibility (χ) -38.4•10−6 cm3/mol
CAS Number:
106-51-4
Molecular Weight:
108.09
Beilstein:
773967
EC Number:
203-405-2
biological source
synthetic
Quality Level
200
grade
reagent grade
vapor density
3.73 (vs air)
vapor pressure
0.1 mmHg ( 25 °C)
Assay
≥98%
form
powder or crystals
autoignition temp.
815 °F
greener alternative product characteristics
Catalysis
Learn more about the Principles of Green Chemistry.
mp
113-115 °C (lit.)
solubility
water: soluble 14.7 g/L at 20 °C
greener alternative category
storage temp.
room temp
SMILES string
O=C1C=CC(=O)C=C1
InChI
1S/C6H4O2/c7-5-1-2-6(8)4-3-5/h1-4H
InChI key
AZQWKYJCGOJGHM-UHFFFAOYSA-N
Gene Information
human ... ACHE(43) , BCHE(590) , CES1(1066)

CAS
106-51-4
Formule moléculaire
C6H4O2
Poids moléculaire (g/mol)
108.096
Numéro MDL
MFCD00001591
Clé InChI
AZQWKYJCGOJGHM-UHFFFAOYSA-NAfficher plus
Synonyme
p-benzoquinone, benzoquinone, quinone, 1,4-benzoquinone, p-quinone, chinone, 2,5-cyclohexadiene-1,4-dione, cyclohexadienedione, para-quinone, 1,4-benzoquineAfficher plus
CID PubChem
4650
ChEBI
CHEBI:16509
Nom IUPAC
cyclohexa-2,5-diène-1,4-dione
SMILES
C1=CC(=O)C=CC1=O
Chemical name or material p-Benzoquinone
Fusion point 112°C to 115°C
Density 1.318
Boiling point ∼180°C (sublimation)
Flash point 77°C (171°F)
Dosage percentage range ≥98%
Smell Pungent
Quantity 100 g
Number one UN2587
Beilstein 773967
Sensitivity Light sensitive
Merck Index 14,8074
Solubility Information Soluble in water,ethanol,ether,methanol,benzene,acetone and ethyl acetate.
Formula weight 108.1
Purity percentage ≥98%
Solubility 10 g/l (25°C)
Melting Point 110 - 113°C
Molar Mass 108.09 g/mol
Bulk Density 700 kg/m3
Boiling Point 180°C (sublimated)
Vapor Pressure 0.12 hPa (20°C)
Density 1.32 g/cm3 (20°C)
pH 4 (1 g/l, H2O, 20°C)
Ignition Point 560°C




SAFETY INFORMATION ABOUT P-BENZOQUINONE:
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product.
PBS-AM
2-PHOSPHONOBUTANE-1,2,4-TRICARBOXYLIC ACID; PBTC; Bayhibit AM; PBS-AM; Phosphonobutanetricarboxylic acid; 2-Phosphono-1,2,4-butanecarboxylic acid; CAS NO: 37971-36-1
PBTC
SYNONYMS PBTC; Bayhibit AM; PBS-AM; Phosphonobutanetricarboxylic acid; 2-Phosphono-1,2,4-butanecarboxylic acid; CAS NO. 37971-36-1
PBTC ( 2-PHOSPHONOBUTANE-1,2,4-TRICARBOXYLIC ACID)
Synonyms: PBTCA; PBTC; Phosphonobutane tricarboxylic Acid; 2-Phosphonobutane-1,2,4-Tricarboxylic Acid; PBS-AM; Phosphonobutanetricarboxylic acid; 2-Phosphono-1,2,4-butanecarboxylic acid; Phosphonono Butanetricarboxylic Acid; 2-phosphono-1,2,4-butanetricarboxylic acid. cas :40372-66-5
PBTCA
2-Phosphonobutane -1,2,4-Tricarboxylic Acid; PBTC;PBTCA;PHOSPHONOBUTANE TRICARBOXYLIC ACID;2-Phosphonobutane -1,2,4-Tricarboxylic Acid;2-Phosphonobutane-1,2,4-tricarboxylic acid PBTC; PBTC; Bayhibit AM; PBS-AM; Phosphonobutanetricarboxylic acid; 2-Phosphono-1,2,4-butanecarboxylic acid; CAS NO:37971-36-1
PBTCA (2-PHOSPHONOBUTANE-1,2,4-TRICARBOXYLIC ACID 
P-CHLORO-M-CRESOL, N° CAS : 59-50-7. Nom INCI : P-CHLORO-M-CRESOL. Nom chimique : 4-Chloro-3-methylphenol. chlorocresol . Synonymes : 4-chloro-m-cresol;p-Chloro-m-crésol;Chlorocrésol;4-Chloro-3-méthylphenol;2-Chloro-5-hydroxytoluene;2-CHLORO-HYDROXYTOLUENE;4-Chloro-1-hydroxy-3-methylbenzene;4-chloro-3-cresol;4-Chloro-3-hydroxytoluene;4-chloro-3-methyl phenol;4-CHLORO-META-CRESOL;6-CHLORO-3-HYDROXYTOLUENE;6-Chloro-m-cresol;AI3-00075;APTAL;BAKTOL;BAKTOLAN;CANDASEPTIC;Caswell No 185A;Chlorocresolo;Chlorocrésol;Chlorocresolo; Chlorocresolum (Latin); Chlorokresolum; Clorocresol (Spanish); EPA Pesticide Chemical Code 064206;m-Cresol, 4-chloro-; OTTAFACT; P-CHLOR-M-CRESOL; p-Chloro-m-crésol;P-CHLOROCRESOL;Parachlorometacresol;PARMETOL;PAROL;PCMC;PERITONAN;Phenol, 4-chloro-3-methyl-;PREVENTOL CMK;RASCHIT;RASCHIT K;RASEN-ANICON;RCRA waste number U039 ;N° EINECS/ELINCS : 200-431-6. Classification : Règlementé, Conservateur, Ses fonctions (INCI), Conservateur : Inhibe le développement des micro-organismes dans les produits cosmétiques.Noms français : 2-CHLORO-5-HYDROXYTOLUENE; 2-CHLORO-HYDROXYTOLUENE; 3-METHYL-4-CHLOROPHENOL; 4-CHLORO-3-METHYLPHENOL; 4-CHLORO-5-METHYLPHENOL ; 4-CHLORO-M-CRESOL; 4-CHLOROCRESOL; 4-CHLOROCRESOL (META-); 6-CHLORO-3-HYDROXYTOLUENE; 6-CHLORO-M-CRESOL; CHLORO-4 HYDROXY-3 TOLUENE; CHLORO-4 METHYL-3 PHENOL;Chloro-4 méthyl-3 phénol; M-CRESOL, 4-CHLORO; P-CHLOR-M-CRESOL; P-CHLORO-M-CRESOL; p-Chlorocresol; p-Chlorocrésol; PHENOL, 4-CHLORO-3-METHYL; PHENOL, 4-CHLORO-3-METHYL-. Noms anglais : p-Chlorocresol. Utilisation et sources d'émission : Agent désinfectant, agent antiseptique. 1237629 [Beilstein]; 200-431-6 [EINECS]; 441; 4-Chlor-3-methylphenol [German] ; 4-Chloro-3-methylphenol [ACD/IUPAC Name]; 4-Chloro-3-méthylphénol [French] [ACD/IUPAC Name]; 4-Chloro-m-cresol; 59-50-7 [RN]; chlorocresol; chlorocrésol [French] ; clorocresol [Spanish] ; GO7100000; p-Chlorocresol [Wiki]; p-Chloro-m-cresol; PCMC; Phenol, 4-chloro-3-methyl- [ACD/Index Name]; QR BG E1 [WLN]; хлорокрезол [Russian]; كلوروكريسول [Arabic]; 122307-41-9 [RN]; 1-Chloro-2-methyl-4-hydroxybenzene; 2-Chloro-5-hydroxytoluene; 2-Chloro-hydroxytoluene; 3-hydroxy-10,13-dimethyl-17-(6-methylheptan-2-yl)-1,2,3,4,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-7-one; 4-06-00-02064 (Beilstein Handbook Reference) [Beilstein]; 43M; 4-Chloro-1-hydroxy-3-methylbenzene; 4-Chloro-3-methoxy-2-methylpyridine-n-oxide; 4-chloro-3-methyl-phenol; 4-Chloro-3-Methylphenol (en); 4-Chloro-3-methylphenol 100 ?g/mL in Methanol; 4-Chloro-3-methylphenol 100 µg/mL in Methanol; 4-Chloro-3-methylphenol, BP, EP grade; 4-Chloro-3-methylphenol-2,6-d2; 4-Chloro-5-methylphenol; 4-Chloro-m-cresol;PCMC;Chlorocresol; 6-Chloro-3-hydroxytoluene; 6-Chloro-m-cresol; 93951-72-5 [RN]; Aptal; Baktol; Baktolan; C006984; Candaseptic; Chlorcresolum; Chlorkresolum; Chloro-3-cresol; Chlorocresol (4-Chloro-3-methylphenol); Chlorocresol (NF); Chlorocresol [USAN:INN]; Chlorocresolo; Chlorocresolum [INN-Latin]; Chlorocresolum [Latin]; Chlorokresolum; Clorocresol [INN-Spanish]; Clorocresol [Spanish]; Clorocresolo [DCIT]; CMK; EINECS 200-431-6; HSCI1_000352; DI1_000768; InChI=1/C7H7ClO/c1-5-4-6(9)2-3-7(5)8/h2-4,9H,1H Lysochlor; m-Cresol, 4-chloro-; NCGC00091338-02; Ottafact; para-Chloro-meta-cresol; Parachlorometacresol; parmatol; Parmetol; Parol [Wiki]; p-Chlor-m-cresol; Peritonan; Pharmakon1600-01500178; PHEN-2,6-D2-OL,4-CHLORO-3-METHYL- (9CI); Phenol, 4-chloro-5-methyl-; Preventol CMK; Raschit; Raschit K; 4-chloro-3-methylphenol; 4-chloro-m-cresol; chlorocresol; 4-chloro-m-cresol; 4-chloro-3-methylphenol; chlorocresol;4-chloro-m-cresol;4-chloro-3-methylphenol; Phenol, 4-chloro-3-methyl-. Translated names : 4-chlor-3-methylfenol (cs) ; 4-Chlor-3-methylphenol (de); 4-chlor-3-metilfenolis (lt); 4-Chlor-m-kresol (de); 4-chlor-m-krezolis, (lt); 4-chloro-3-metylofenol (pl); 4-chloro-3-méthylphénol (fr); 4-chloro-m-crésol (fr); 4-chloro-m-krezol (pl); 4-chlór-3-metylfenol (sk); 4-chlór-meta-krezol (sk); 4-clor-3-metilfenol (ro); 4-clor-m-cresol (ro); 4-cloro-3-metilfenol (es); 4-cloro-m-cresol (es); 4-hlor-3-metilfenols (lv); 4-hlor-m-krezols (lv); 4-kloori-3-metyylifenoli (fi); 4-klor-3-metylfenol (no); 4-klor-m-kresol (no); 4-kloro-3-metil-fenol (hr); 4-kloro-3-metilfenol (sl); 4-kloro-3-metüülfenool (et); 4-kloro-m-kresool (et); 4-kloro-m-krezol (hr); 4-klór-3-metilfenol (hu); 4-klór-m-krezol (hu); 4-хлоро-3-метилфенол (bg); 4-хлоро-m-крезол (bg); Chloorkresol (nl); chlorcresol (da); chlorkresol (cs); Chlorkrezolis (lt); chlorocresol (da); Chlorocrésol (fr); Chlorokresol (de); chlórkrezol (sk); clor crezol (ro); Clorocresol (es); Clorocresolo (it); Clorocrezol (ro); Hlorkrezols (lv); kloorikresoli (fi); klorkresol (no); Klorokresol (mt); Klorokresoli (fi); Klorokresool (et); Klorokrezol (hr); klórkrezol (hu); χλωροκρεζόλη (el); Χλωροκρεσόλη (el); Хлорокрезол (bg). : 4-Chlor- 3-methylphenol; 4-chloro-3-methyl phenol; 4-Chloro-m-cresol, PCMC, 2-Chloro-5-hydroxytoluene; p-chloro-m-cresol
PC (PROPYLENE CARBONATE)
Propylene carbonate (PC) is a cyclic carbonate that is commonly used as a solvent and as a reactive intermediate in organic synthesis.
Propylene carbonate (PC) is being considered as a potential electrochemical solvent due to its low vapor pressure, high dielectric constant and high chemical stability.

CAS Number: 108-32-7
Molecular Weight: 102.09
EC Number: 203-572-1
Molecular formula: CH3C2H3O2CO


Propylene carbonate (PC) can be synthesized from propylene oxide and CO2.
Optically active form of Propylene carbonate (PC) can be prepared from the reaction between CO2 and racemic epoxides.
Decomposition of Propylene carbonate (PC) on the graphite electrode in lithium batteries results in the formation of a lithium intercalated compound.

Propylene carbonate (PC) is a colorless, odorless liquid with a high boiling point and low volatility.
Propylene carbonate (PC) is widely used as a solvent in various industries.

Propylene carbonate (PC) is widely produced for commercial and industrial use.
It is synthesized via the carbonation of Propylene Oxide.
One of Propylene carbonate (PC) primary industrial uses are as a solvent—in particular, as an aprotic solvent and racemate.

Propylene carbonate (PC) has a very high molecular dipole moment.
This means that numerous elements and compounds can be dissolved in PC, such as potassium, sodium, and other alkali metals by electrolysis of their chlorides.
Propylene carbonate (PC) is often used as a solvent in petroleum products and oil field services, specifically to remove carbon dioxide from natural gas and refined gas.

Propylene carbonate (PC) is a VOC-exempt clear polar solvent having high boiling andflash points, a low order of toxicity and a mild ether-like odor.
It is stable under most conditions and is not hydroscopic or corrosive.
Propylene carbonate (PC) is particularly well suited for applications requiring a water white product or high purity.

Propylene carbonate (PC) is a clear, organic polar solvent made from the reaction of propylene with carbon dioxide.
​Propylene Carbonate (PC) is a PU-plasticizer and it is VOC-free clear polar solvent having high boiling and flashpoints.
Propylene carbonate (PC) is a clear, odorless solvent with a high boiling point.

In cosmetics and personal care products, Propylene Carbonate is used in the formulation of makeup, primarily lipstick, eye shadow, and mascara, as well as in skin cleansing
products
Propylene carbonate (PC) is an excellent solvent for a variety of substances, particularly those that are polar or have high polarity.
Propylene carbonate (PC)'s often used in formulations for paints, coatings, adhesives, and inks.

Propylene carbonate (often abbreviated PC) is an organic compound with the formula C4H6O3.
It is a cyclic carbonate ester derived from propylene glycol.
This colorless and odorless liquid is useful as a polar, aprotic solvent.

Propylene carbonate (PC) is chiral, but is used as the racemic mixture in most contexts.
Propylene carbonate has a cyclic carbonate structure with three carbon atoms and three oxygen atoms in the ring.
Propylene carbonate (PC) is a clear, colorless liquid at room temperature.

Propylene carbonate (PC) is nearly odorless.
The boiling point of propylene carbonate is relatively high, around 240°C (464°F).
Propylene carbonate (PC) has a relatively high density compared to many common solvents.

Propylene carbonate (PC) is miscible with water and many organic solvents.
Its ability to dissolve both polar and nonpolar substances is one of its key features.
Propylene carbonate (PC) has a low flammability and high flash point, making it relatively safe to handle.

Propylene carbonate (often abbreviated PC) is an organic compound with the formula CH3C2H3O2CO.
It is a carbonate ester derived from propylene glycol.
This colorless and odorless liquid is useful as a polar, aprotic solvent.

Propylene carbonate (PC) is chiral but is used exclusively as the racemic mixture.
Propylene Carbonate (PC) is a carbonate ester derived from propylene glycol with the peculiarity to have a low order of toxicity and a mild ether-like odor.
Propylene carbonate (PC) is stable under most conditions and it is not hydroscopic or corrosive.

Propylene carbonate (PC) is usually produced through the reaction of propylene oxide with carbon dioxide.
This reaction is catalyzed by various catalysts to yield Propylene carbonate (PC) and other byproducts.
The process can be performed under pressure and elevated temperature.

Although many organic carbonates are produced using phosgene, Propylene carbonate (PC)s are exceptions.
They are mainly prepared by the carbonation of the epoxides (epoxypropane, or propylene oxide here):
CH3CHCH2O + CO2 → CH3C2H3O2CO

The process is particularly attractive since the production of these epoxides consumes carbon dioxide.
Thus this reaction is a good example of a green process.
The corresponding reaction of 1,2-propanediol with phosgene is complex, yielding not only Propylene carbonate (PC) but also oligomeric products.

Propylene carbonate (PC) can also be synthesized from urea and propylene glycol over zinc acetate.
Propylene carbonate (PC) is a colorless liquid freezing at -48.8°C and boiling at 242°C.
Propylene carbonate has a vapor pressure of 0.13 mmHg at 20°C, and 0.98 mmHg at 50°C.

grade: anhydrous
Quality Level: 100
vapor pressure: 0.13 mmHg ( 20 °C), 0.98 mmHg ( 50 °C)
Assay: 99.7%
form: liquid
autoignition temp.: 851 °F
expl. lim.: 14.3 %
impurities: <0.002% water, <0.005% water (100 mL pkg)
refractive index: n20/D 1.421 (lit.)
pH: 7 (20 °C, 200 g/L)
bp: 240 °C (lit.)
mp: −55 °C (lit.)
density: 1.204 g/mL at 25 °C (lit.)
Melting point: -49°C,
Boiling point:240-243°C,
Refractive index:1.4189 (20 °C)
Viscosity:2.5mPas

Propylene carbonate (PC) is prevalent in chemical intermediates, paints/coatings, dyes, fibers, as a reactive diluent in urethane systems, wood binder resins, safer alternative in cosmetic/personal care formulations, and as electrolyte solvents for lithium batteries (among many more).
Propylene carbonate (PC) is a polar aprotic solvent used as a “green” sustainable alternative solvent for chemical transformations.

Propylene carbonate (PC) is a low toxicity, biodegradable, non-corrosive colorless liquid with a high boiling point, low vapor pressure, and EPA VOC exemption.
Due to its low vapor pressure and findings of negligible photochemical reactivity, Propylene carbonate (PC) is an effective substitute for more hazardous solvents such a MEK, methylene chloride, toluene, acetone, NMP, and perchloroethylene.

Propylene carbonate (PC) is also compatible with other solvents providing an efficient ingredient in co-solvent formulations.
It is widely used in the manufacture of paints, adhesives, coatings, surface cleaners, degreasers, strippers, and inks formulations as well as in lithium-ion batteries, as electrolytic solvent, and in the removal of carbon dioxide from natural gas.

Propylene carbonate (PC) is another important cyclic carbonate solvent in Lithium-ion Batteries (LIB) Electrolyte.
This carbonate improves the high-temperature performance of LIB but more Propylene carbonate (PC) deteriorates the cycling and rate capability of LIB due to its incompatibility to the graphite.

Propylene carbonate (PC) has a high boiling point, high viscosity, and high dielectric constant.
The viscosity of Propylene carbonate (PC) is the highest among commonly used organic carbonates, which lowers the ionic mobility and conductivity of the electrolyte.
Therefore, Propylene Carbonate takes less than 5% in most of the commercial LIB electrolytes.

Propylene carbonate (PC) or PC is an organic compound derivative of propylene glycol.
Propylene carbonate (PC) is alternatively manufactured from propylene mixed with carbon dioxide.
It is available as a clear, odorless liquid.

Propylene carbonate (PC) works as a solvent in cleaning and degreasing.
It is preferred over similar chemicals like acetone and ethyl acetate due to its molecular structure, versatility, soil-stripping properties, and broad compatibility
with other solvents.
It is used to clean and degrease circuit boards, carburetors, ink cleaners, polymers, resins, and industrial cleanup.

Propylene carbonate (PC) is relatively safe to use. Studies indicate that it does not irritate naked skin when handled in cosmetic applications.
Propylene carbonate (PC) has a high boiling point, its vapor is inconsequential, and it is not associated with any toxicities.
It is readily biodegradable and has no photochemical reactivity.

Propylene carbonate (PC) is a colorless liquid.
Propylene carbonate (PC) is used in paints as a highboiling solvent and film-forming auxiliary, especially in poly(vinyl fluoride) and poly(vinylidene fluoride) systems.
It is also employed as an auxiliary in the pigment and dye industry.

Propylene carbonate (PC) can be found in adhesive formulations, contributing to their performance and workability.
Propylene carbonate (PC)'s used as a solvent for natural gas purification and as a component in drilling fluids.
In addition to cosmetics, propylene carbonate is used in some personal care items such as nail polish removers and cuticle treatments.

Propylene carbonate (PC)'s employed as a solvent in pharmaceutical formulations, especially for poorly soluble drugs.
Propylene carbonate (PC)'s solvency power makes it effective in various cleaning products, including graffiti removers and industrial degreasers.

Propylene carbonate (PC)'s ability to dissolve a wide range of substances, both polar and nonpolar, makes it versatile in various applications.
Its low volatility reduces the risk of hazardous vapors being released into the environment during use.
It is chemically stable under many conditions, which contributes to its long shelf life and usability.

Compared to some other organic solvents, Propylene carbonate (PC) is relatively environmentally friendly.
This property is beneficial in applications requiring a high dielectric constant, such as in capacitors and electronic devices.

Uses
Propylene carbonate (PC) is used as a polar, aprotic solvent.
Propylene carbonate (PC) has a high molecular dipole moment (4.9 D), considerably higher than those of acetone (2.91 D) and ethyl acetate (1.78 D).
Propylene carbonate (PC) is possible, for example, to obtain potassium, sodium, and other alkali metals by electrolysis of their chlorides and other salts dissolved in propylene carbonate.

Propylene carbonate (PC) is used mainly as a solvent in oral and topical pharmaceutical formulations.
In topical applications, Propylene carbonate (PC) has been used in combination with propylene glycol as a solvent for corticosteroids.
The corticosteroid is dissolved in the solvent mixture to yield microdroplets that can then be dispersed in petrolatum.

Propylene carbonate (PC) has been used as a dispensing solvent in topical preparations.
Propylene carbonate (PC) has also been used in hard gelatin capsules as a nonvolatile, stabilizing, liquid carrier.
For formulations with a low dosage of active drug, a uniform drug content may be obtained by dissolving the drug in propylene carbonate and then spraying this solution on to a solid carrier such as compressible sugar; the sugar may then be filled into hard gelatin capsules.

Propylene carbonate (PC) may additionally be used as a solvent, at room and elevated temperatures, for many cellulose-based polymers and plasticizers.
Propylene carbonate (PC) is also used in cosmetics.

Other usages of Propylene carbonate (PC) include its function as a component of electrolytes in lithium batteries.
Propylene carbonate (PC) also has uses as a component for adhesives, and for coatings products like paints.
Its other uses include in electronic materials, in inks and digital ink products, and as a textile auxiliary.

Propylene carbonate (PC) is often used as a solvent for electrolysis.
Propylene carbonate (PC) is used on its own and in a variety of end-use cleaning and degreasing formulations due to its versatility, effectiveness in reducing surface tension, and ability to improve wetting and soil removal functionality.
Formulators also incorporate propylene carbonate into water rinsable solvent systems.

Propylene carbonate (PC) is used as a chemical intermediate in the production of various chemicals, including plasticizers, lubricants, and pharmaceuticals.
Due to its low toxicity and ability to solubilize a wide range of cosmetic ingredients, Propylene carbonate (PC) is used in products such as skin creams, lotions, and hair care products.

Propylene carbonate (PC)'s utilized in industrial cleaning products and degreasers due to its effectiveness in dissolving oils, greases, and other contaminants.
Propylene carbonate (PC) can be found in certain paint and coating formulations as a solvent and viscosity modifier.

Propylene carbonate (PC) is used as a solvent in various chemical reactions, particularly those that involve high temperatures or polar and nonpolar substances.
It's often chosen as a reaction medium due to its ability to dissolve a wide range of compounds.
One of the most significant applications of propylene carbonate is as a solvent in the electrolyte of lithium-ion batteries.

Propylene carbonate (PC) helps improve the mobility of lithium ions between the battery's electrodes, contributing to the battery's overall performance, capacity, and cycle life.
Similar to its use in batteries, propylene carbonate is employed in electrochemical capacitors, also known as supercapacitors.
Propylene carbonate (PC) aids in enhancing the energy storage capabilities of these devices.

In the paint and coating industry, propylene carbonate is used as a coalescing agent in water-based formulations.
Propylene carbonate (PC) promotes the fusion of polymer particles, allowing the formation of a continuous film that enhances the coating's durability and appearance.

Propylene carbonate (PC) can be found in adhesive and sealant formulations, contributing to their performance by improving viscosity and workability.
Due to its low toxicity and ability to dissolve a variety of cosmetic ingredients, propylene carbonate is used in personal care products such as skin creams, lotions, hair care products, and cosmetics.

Propylene carbonate (PC) is used as a solvent in pharmaceutical applications, assisting in the formulation of certain drugs, especially those with low solubility in water.
Its excellent solvency properties make it effective in cleaning products, such as graffiti removers, industrial degreasers, and household cleaning solutions.
Propylene carbonate (PC) is used in the oil and gas industry as a solvent for natural gas purification and as a component in drilling fluids.

Propylene carbonate (PC) serves as a chemical intermediate in the production of various chemicals, including plasticizers, lubricants, and specialty chemicals.
Due to its high dielectric constant, it can be used in electronics applications requiring materials with specific dielectric properties.
It can also be used in various chemical reactions as a solvent, particularly those involving high temperatures.

Propylene carbonate (PC) is particularly well suited for applications requiring a water-white product or high purity.
It can be used in cosmetics and personal care products; mainly in the formulation of make-up, primarily lipstick, eye shadow, and mascara, as well as in skin cleansing products.

Being a cyclic carbonate reacts with amines to form carbamates, undergoes hydroxy alkylation and transesterification Propylene carbonate (PC) can be used as an isocyanate and unsaturated polyester resin cleanup solvent, viscosity reducer in coatings, CO2 extraction solvent, electrolyte in lithium batteries, polar additive for clay gellants, foundry binder catalyst, and textile dye carrier and cleaner.

Safety
Propylene carbonate (PC) does not cause skin irritation or sensitization when used in cosmetic preparations, whereas moderate skin irritation is observed when used undiluted. No significant toxic effects were observed in rats fed propylene carbonate, exposed to the vapor, or exposed to the undiluted liquid.
In the US, Propylene carbonate (PC) is not regulated as a volatile organic compound (VOC) because it does not contribute significantly to the formation of smog and because its vapor is not known or suspected to cause cancer or other toxic effects.

Propylene carbonate (PC) is stable under normal storage conditions.
However, in the presence of an acid, base, metal oxide or salt, propylene carbonate may decompose liberating CO2.
These materials will also decrease thermal stability. In an aqueous solution, the decomposition products would be propylene glycol and CO2.

While Propylene carbonate (PC) is generally considered safe for many applications, it's important to be aware of its potential hazards:
Propylene carbonate (PC) is low in toxicity, it should not be ingested or allowed to come into contact with the skin or eyes.
Proper protective equipment and handling procedures should be followed.

Environmental Impact
Like many chemicals, improper disposal of Propylene carbonate (PC) can have environmental impacts.
It should be handled and disposed of in accordance with local regulations.

Synonyms
PROPYLENE CARBONATE
108-32-7
4-Methyl-1,3-dioxolan-2-one
1,2-Propylene carbonate
1,2-Propanediol cyclic carbonate
Texacar PC
Arconate 5000
Cyclic propylene carbonate
1,2-Propanediol carbonate
1,3-Dioxolan-2-one, 4-methyl-
Dipropylene carbonate
1-Methylethylene carbonate
4-Methyldioxalone-2
1,2-Propanediyl carbonate
Cyclic 1,2-propylene carbonate
Propylene glycol cyclic carbonate
Cyclic methylethylene carbonate
4-Methyl-2-oxo-1,3-dioxolane
Carbonic acid, propylene ester
NSC 11784
Carbonic acid, cyclic propylene ester
Propylenester kyseliny uhlicite
HSDB 6806
Carbonic acid cyclic methylethylene ester
EINECS 203-572-1
Carbonic acid, cyclic propylene ether
NSC-11784
UNII-8D08K3S51E
BRN 0107913
DTXSID2026789
AI3-19724
8D08K3S51E
PC-HP
Propylenecarbonate, 99%
Propylene carbonate [NF]
Propylene carbonate [USAN]
Propylenester kyseliny uhlicite [Czech]
DTXCID006789
EC 203-572-1
5-19-04-00021 (Beilstein Handbook Reference)
Propylene carbonate (NF)
WLN: T5OVOTJ D
PROPYLENE CARBONATE (II)
PROPYLENE CARBONATE [II]
PROPYLENE CARBONATE (MART.)
PROPYLENE CARBONATE [MART.]
PROPYLENE CARBONATE (USP-RS)
PROPYLENE CARBONATE [USP-RS]
CAS-108-32-7
4-methyl-1,3-dioxolane-2-one
butylhexanoate
MFCD00798264
MFCD00798265
Arconate HP
Solvenon PC
Jeffsol PC
propylen carbonate
?Propylene carbonate
MFCD00005385
Carbonate de propylne
Arconate 1000
Carbonic acid propylene
Jeffsol AG 1555
1 2-Propylene carbonate
Arconate propylenecarbonate
1,2-propanodiol carbonato
1 2-Propanediol carbonate
1 2-Propanediyl carbonate
Arconate propylene carbonate
1-carbonato de metiletileno
1,2-carbonato de propileno
Propylene carbonate, 1,2-
SCHEMBL15309
1-propanediol cyclic carbonate
2-oxo-4-metil-1,3-dioxolano
4-metil-1,3-dioxolano-2-ona
Cyclic 1 2-propylene carbonate
(S)-1,2-Propanediol carbonate
4-Methyl-1 3-dioxolan-2-one
CHEMBL1733973
2-Oxo-4-methyl-1 3-dioxolane
2-Oxo-4-methyl-1,3-dioxolane
4-Methyl-1 3-dioxolane-2-one
4-Methyl-2-oxo-1 3-dioxolane
1 2-Propanediol cyclic carbonate
1,2-PDC
4-methyl-[1,3]dioxolan-2-one
NSC1913
1,2-carbonato de propanodiilimino
2-Methyl-1 2-ethylene carbonate
1,3-dioxolan-2-ona, 4-metil-
1,3-dioxolane-2-one, 4-methyl
PROPYLENE CARBONATE [HSDB]
PROPYLENE CARBONATE [INCI]
2-metil-1,2-carbonato de etileno
PROPYLENE CARBONATE [VANDF]
NSC 1913
NSC-1913
NSC11784
Propylene carbonate (Battery grade)
Tox21_202047
Tox21_303214
BBL027518
Carbonic acid propylene ester (6CI)
STL373011
AKOS009158417
Propylene Carbonate (Industrial Grade)
SB66353
Propylene carbonate, anhydrous, 99.7%
NCGC00165974-01
NCGC00165974-02
NCGC00256995-01
NCGC00259596-01
Propylene carbonate, for HPLC, 99.7%
BP-30108
BP-31155
Carbonic acid cyclic 1 2-propylene ester
LS-51953
SY008770
SY066861
Carbonic acid cyclic propylene ester (8CI)
Propylene carbonate, ReagentPlus(R), 99%
CS-0076373
FT-0602265
FT-0639979
FT-0660009
FT-0674103
P0525
D05633
EN300-296359
Propylene carbonate, anhydrous, Water 50ppm Max.
Propylene carbonate, Selectophore(TM), >=99.0%
Q415979
J-002116
Propylene carbonate, Vetec(TM) reagent grade, 98%
F0001-0165
Propylene carbonate, >=99%, acid 1,2-Propanediol cyclic carbonate, 4-Methyl-1,3-dioxolan-2-one
Propylene carbonate, United States Pharmacopeia (USP) Reference Standard
110320-40-6
P-CHLOROCRESOL
p-Chlorocresol, also called 4-Chloro-3-methylphenol, is a white to almost white flake.
p-Chlorocresol is an efficient anti-mould antiseptic, frequently used in personal care products.
p-Chlorocresol, is the organic compound with the formula C7H7ClO.

CAS Number: 59-50-7
Molecular Formula: C7H7ClO
Molecular Weight: 142.58
EINECS Number: 200-431-6

p-Chlorocresol is a monochlorinated m-cresol.
p-Chlorocresol is a white or colorless solid that is only slightly soluble in water.
As a solution in alcohol and in combination with other phenols, it is used as an antiseptic and preservative.

p-Chlorocresol is a moderate allergen for sensitive skin.
p-Chlorocresol, also known as parachlorocresol or PCMC, is a chemical compound with the molecular formula C7H7ClO.
p-Chlorocresol is a chlorinated derivative of cresol, which is a type of aromatic hydrocarbon.

p-Chlorocresol, or 4-chloro-3-methylphenol (ClC6H3CH3OH), also known as p-chloro-m-cresol, is a potent disinfectant and antiseptic.
p-Chlorocresol appears as a pinkish white crystalline solid and has a melting point of 64-66°C.
p-Chlorocresol is also used as a preservative in cosmetics and medicinal products for both humans and animals.

p-Chlorocresol is used as an active ingredient in some preparations of veterinary medicines for tropical, oral and parenteral use.
Normally, the concentration of p-Chlorocresol in oral and parenteral veterinary products are 0.1-0.2%.
Concentrations are higher (~0.5%) in tropical veterinary products.

p-Chlorocresol contains microbial activity against both gram positive and gram negative bacteria and fungi.
The use of p-Chlorocresol is regulated by government agencies such as the US Food and Drug administration, and limits are set on the amount of p-Chlorocresol that can be present in various products.
p-Chlorocresol colorless, white, or pinkish crystals with a slight phenolic odor.

p-Chlorocresol is white (pure) or pink crystalline solid.
Crystals turn pink on exposure to air and light.
P-Chlorocresol (p-chloro-m-cresol; PCMC; brand name: Preventol CMK) is a chlorinated phenol which is used as an antiseptic and preservative.

p-Chlorocresol forms colourless, dimorphous crystals at room temperature and is only slightly soluble in water.
For use as a disinfectant such as a hand wash, it is commonly dissolved in alcohol in combination with other phenols.
p-Chlorocresol is a moderate allergen for sensitive skin.

p-Chlorocresol is used as a preservative in a wide number of topical preparations and is a rare cause of allergic contact dermatitis and CoU, the mechanism of which remains uncertain.
A pinkish to white crystalline solid with a phenolic odor.
Shipped as a solid or in a liquid carrier.

p-Chlorocresol (p-chloro-m-cresol; PCMC; brand name: Preventol CMK) possesses disinfectant and antiseptic properties.
p-Chlorocresol is used in various preparations for skin disinfection and wounds.
p-Chlorocresol also used as a preservative in creams and other preparations for external use which contain water.

For use as a disinfectant such as a hand wash, p-Chlorocresol is commonly dissolved in alcohol in combination with other phenols.
p-Chlorocresol is a moderate allergen for sensitive skin.
p-Chlorocresol produces potentially life-threatening effects which include dermatitis, which are responsible for the discontinuation of chlorocresol therapy.

The symptomatic adverse reactions produced by chlorocresol are more or less tolerable and if they become severe, they can be treated symptomatically, these include hypersensitivity reactions, irritation of eyes.
p-Chlorocresol is synthesized from the monochlorination of 3-methylphenol at position 4.
This is a p-Chlorocresol used as an antiseptic, disinfectant and fungicide.

p-Chlorocresol is found in reams, topical antiseptics, shampoos, cosmetics and cooling fluids.
p-Chlorocresol is also used as an ingredient in various pharmaceutical preparations.
Further research may identify additional p-Chlorocresol or industrial usages of this chemical.

p-Chlorocresol is a monochlorinated m-cresol.
p-Chlorocresol is prepared by the chlorination of m-cresol.
Freely soluble in organic solvent, ether, ketones and strong base aqueous solution, and completely soluble in oil.

Friendly to environment, formaldehyde-free, easily degradable.
Well compatibility with anionic surfactant, non-ionic surfactant and emulgator.
Good synergistic effect with other antiseptic and bactericide.

p-Chlorocresol white to slightly pink crystals.
The chemical structure of p-Chlorocresol consists of a phenolic ring (cresol) with a chlorine atom (Cl) attached to the para position, meaning it is located opposite to the hydroxyl (OH) group.
p-Chlorocresol has antimicrobial properties and has been used as an antiseptic and preservative in various pharmaceutical and personal care products.

p-Chlorocresol helps prevent the growth of bacteria and fungi.
p-Chlorocresol has been employed in wood preservation to protect wood from decay and fungal growth.
p-Chlorocresol has been used in topical medications, including creams and ointments.

p-Chlorocresol exhibits broad-spectrum antimicrobial activity, making it effective against a range of microorganisms, including bacteria and fungi.
While p-Chlorocresol has been used in certain applications, its use has been subject to regulations and guidelines due to potential concerns about skin irritation and sensitization.
The concentration of p-Chlorocresol in products is often regulated, and its inclusion in formulations is carefully considered.

p-Chlorocresol can be synthesized through the chlorination of cresol, typically using chlorine gas.
p-Chlorocresol is odorless or slightly phenolic odor.
p-Chlorocresol, soluble in alkalies, organic solvents, fats, and oils.

p-Chlorocresol is a monochlorinated m-cresol.
p-Chlorocresol is a white or colorless solid that is only slightly soluble in water.
p-Chlorocresol is prepared by chlorination of m-cresol.

p-Chlorocresol forms colourless, dimorphous crystals at room temperature and is only slightly soluble in water.
p-Chlorocresol is the organic compound with the formula ClC6H4OH.
p-Chlorocresol is a monochlorinated m-cresol.

p-Chlorocresol is done in the liver, and then excreted primarily via the kidneys or in smaller amounts through the lungs.
In facultative Thauera sp. strain DO, p-Chlorocresol was degraded aerobically either by dehalogenation followed by catechol degradation pathway, or methyl oxidation to 4-chlorobenzoate.
The exact reaction mechanism in humans is unknown.

Oxidation The oxidation reaction of p-Chlorocresol by hydrogen peroxide (H2O2) can occur through a two-step process.
In the first step, H2O2 is activated by a catalyst, such as a metal ion or an enzyme, to form a reactive oxygen species, such as a hydroxyl radical (HO•).
This reactive species can then attack the aromatic ring of the 4-chloro-3-methylphenol molecule, leading to the formation of a quinone intermediate.

p-Chlorocresol is dissolved in organic solvents or nonionic surfactants such as L-64 and then matched with other ingredients.
White or of- white powder or crystlline power,odorless.
Very soluble in N,N-Dimethylformamide, soluble in methanol, sparingly soluble inglacial acetic acid, very slightly soluble inchloroform, practically insoluble in water.

p-Chlorocresol has a broad and very balanced spectrum of activity covering Gram-positive and Gram-negative bacteria, mould and yeast.
The quinone intermediate is an important intermediate in many biological and chemical processes.
p-Chlorocresol can undergo further oxidation to form a variety of compounds, including hydroquinones, catechols, and benzoquinones.

In the case of p-Chlorocresol, the quinone intermediate can be further oxidized to form 4-chlorocatechol, which is a catechol compound.
p-Chlorocresol is a potent disinfectant and antiseptic agent due to its antimicrobial and antifungal properties and is therefore used for wound and skin disinfection.
p-Chlorocresol also has preservative properties and is commonly found in topical creams and cosmetics.

These properties also allow it to be used in paints and inks.
A phenolic preservative agent, the bacteriostatic mechanism of p-Chlorocresol arises from its ability to induce cytoplasmic leakage in bacteria, disrupting membrane permeability to potassium and phosphate ions.
Cytoplasmic leakage also results in dissipation of the proton motive force, causing uncoupling of respiration from ATP synthesis.

p-Chlorocresol is a hydroxytoluene and a member of monochlorobenzenes.
p-Chlorocresol is soluble in water, fatty oil, alkali hydroxide solution and organic solvents such as alcohols, ethers & ketones.
p-Chlorocresol appears as a pinkish to white crystalline solid with a phenolic odor.

p-Chlorocresol is a white or colorless solid that is only slightly soluble in water.
A pinkish to white crystalline solid with a phenolic odor.
p-Chlorocresol forms colourless, dimorphous crystals at room temperature and is only slightly soluble in water.

p-Chlorocresol has a broad and very balanced spectrum of activity covering Gram-positive and Gram-negative bacteria, mould and
yeast.
p-Chlorocresol CAS 59-50-7 or 4-Chloro-3-methylphenol is colorless crystals with phenol odor.
p-Chlorocresol is insoluble in water, soluble in most organic solvents.

p-Chlorocresol with a chemical formula C7H7ClO appears as a white crystalline powdered with a phenolic odor.
p-Chlorocresol is not natural, rather made by human being.
p-Chlorocresol has a broad and very balanced spectrum of activity covering Gram-positive and Gram-negative bacteria, mould and yeast.

Particularly effective against putrefactive bacteria and therefore suitable for use in products which are difficult to preserve (e.g. protein-based formulations).
p-Chlorocresol is a hydroxytoluene that is 3-methylphenol which is substituted by a chlorine at position 4.
p-Chlorocresol has a role as a ryanodine receptor agonist, an antimicrobial agent and a disinfectant.

p-Chlorocresol is a hydroxytoluene and a member of monochlorobenzenes.
p-Chlorocresol is a monochlorinated m-cresol.
p-Chlorocresol is a white or colorless solid that is only slightly soluble in water.

As a solution in alcohol and in combination with other phenols, p-Chlorocresol is used as an antiseptic and preservative .
p-Chlorocresol is also an active ingredient in one registered pest control product which is used as a component in concrete admixtures, while the sodium salt form of chlorocresol is present in two registered pest control products.
p-Chlorocresol is the organic compound with the formula ClC6H4OH.

p-Chlorocresol is a monochlorinated m-cresol.
p-Chlorocresol is a white or colorless solid that is only slightly soluble in water.
As a solution in alcohol and in combination with other phenols, p-Chlorocresol is used as an antiseptic and preservative.

Belongs to the class of organic compounds known as meta cresols.
These are aromatic compounds containing a meta-cresol moiety, which consists of a benzene ring bearing a methyl group and a hydroxyl group at ring positions 1 and 3, respectively.
p-Chlorocresol, or 4-chloro-3-methylphenol (ClC6H3CH3OH), also known as p-chloro-m-cresol, is a potent disinfectant and antiseptic. It appears as a pinkish white crystalline solid and has a melting point of 64-66°C.

p-Chlorocresol is also used as a preservative in cosmetics and medicinal products for both humans and animals.
p-Chlorocresol is used as an active ingredient in some preparations of veterinary medicines for tropical, oral and parenteral use.
Normally, the concentration of p-Chlorocresol in oral and parenteral veterinary products are 0.1-0.2%.

Concentrations are higher (~0.5%) in tropical veterinary products.
p-Chlorocresol contains microbial activity against both gram positive and gram negative bacteria and fungi.
p-Chlorocresol is classified as preservative.

p-Chlorocresol is a biocide, which is colorless crystalline compound.
p-Chlorocresol has role antimicrobial agent.
p-Chlorocresol exhibits stability under certain conditions, making it suitable for use in formulations where a preservative with a longer shelf life is desired.

Over time, there has been a trend toward exploring alternative preservatives and antimicrobial agents due to safety concerns and changing regulatory standards.
The cosmetic and pharmaceutical industries often seek safer and more sustainable options.
The safety of p-Chlorocresol is evaluated through various tests, including skin irritation tests and sensitization tests.

Regulatory agencies review these data to establish guidelines for safe usage in consumer products.
Ongoing research in the field of antimicrobial agents and preservatives may lead to the discovery of new compounds or improved formulations.
Researchers are continuously exploring alternatives that are effective, safe, and environmentally friendly.

The use of p-Chlorocresol in different products is subject to compliance with international standards and regulations.
The safety standards and acceptable usage levels may vary by country or region.
The potential environmental impact of p-Chlorocresol is a consideration, especially when products containing this compound are disposed of.

Assessments of its biodegradability and environmental fate contribute to understanding its ecological footprint.
p-Chlorocresol has role disinfectant.
Oxidation The oxidation reaction of p-Chlorocresol by hydrogen peroxide (H2O2) can occur through a two-step process.

In the first step, H2O2 is activated by a catalyst, such as a metal ion or an enzyme, to form a reactive oxygen species, such as a hydroxyl radical (HO•).
This reactive species can then attack the aromatic ring of the 4-chloro-3-methylphenol molecule, leading to the formation of a quinone intermediate.
The quinone intermediate is an important intermediate in many biological and chemical processes.

p-Chlorocresol can undergo further oxidation to form a variety of compounds, including hydroquinones, catechols, and benzoquinones.
In the case of p-Chlorocresol, the quinone intermediate can be further oxidized to form 4-chlorocatechol, which is a catechol compound.
p-Chlorocresol has role ryanodine receptor agonist.

p-Chlorocresol is a monochlorinated m-cresol.
p-Chlorocresol is a white or colorless solid that is only slightly soluble in wat.
p-Chlorocresol is slightly soluble in water(4g/L), easy soluble in organic solvent such as alcohols (96 percent in ethanol), ethers, ketones, etc.

Melting point: 63-65 °C (lit.)
Boiling point: 235 °C (lit.)
Density: 1.370
vapor pressure: refractive index: 1.5449 (estimate)
Flash point: 118 °C
storage temp. .Store below +30°C.
solubility: methanol: soluble1g/10 mL, clear, colorless
pka: pKa 9.55(t = 25) (Uncertain)
form: Tablets
color: White
PH: 6.5 (1g/l, H2O, 20℃)
Water Solubility: 4 g/L (20 ºC)
Merck: 14,2133
BRN: 1237629
Henry's Law Constant: 2.5(x 10-6 atm?m3/mol)at 20 °C (calculated, Mabey et al., 1982)
Stability: Stable. Incompatible with brass, oxidizing agents, copper, copper alloys.
InChIKey: CFKMVGJGLGKFKI-UHFFFAOYSA-N
LogP: 3.100

p-Chlorocresol is a hydroxytoluene that is 3-methylphenol which is substituted by a chlorine at position 4.
p-Chlorocresol is a hydroxytoluene.
p-Chlorocresol is a monochlorobenzenes.

p-Chlorocresol a hydroxytoluene that is 3-methylphenol which is substituted by a chlorine at position 4.
p-Chlorocresol a ryanodine receptor agonist.
p-Chlorocresol has a broad and very balanced spectrum of activity covering Gram-positive and Gram-negative bacteria, mould and yeast.

Besides p-Chlorocresol, this compound is known by other names such as parachlorocresol, 4-chloro-3-methylphenol, and PCMC.
p-Chlorocresol is sparingly soluble in water but is more soluble in organic solvents.
This solubility property influences its use in different formulations.

In the past, p-Chlorocresol has been used as a preservative in certain vaccines to prevent microbial contamination.
However, due to safety concerns and the desire to reduce the use of certain preservatives in vaccines, alternative preservatives are now often used.
Some individuals may exhibit skin sensitivity or allergic reactions to products containing p-Chlorocresol.

Skin irritation or contact dermatitis has been reported in some cases.
As a result, its use in cosmetics and personal care products is regulated, and formulations are designed to minimize the risk of adverse skin reactions.
In addition to its antibacterial properties, p-Chlorocresol also demonstrates antifungal activity.

This property is valuable in preventing the growth of fungi in products where it is used as a preservative.
The use of p-Chlorocresol is subject to regulatory considerations in different countries.
Regulatory agencies assess its safety and efficacy for specific applications, and restrictions or recommended usage levels may be imposed.

The environmental fate and impact of p-Chlorocresol are considerations in its use.
While it may biodegrade to some extent, its persistence and potential environmental impact depend on factors such as concentration, formulation, and the specific environment.
p-Chlorocresol is prepared by chlorination of m-cresol.

p-Chlorocresol is a chlorinated phenol which is used as an antiseptic and preservative.
For use as a disinfectant such as a hand wash, p-Chlorocresol is commonly dissolved in alcohol in combination with other phenols.
Due to its antimicrobial properties, p-Chlorocresol has been used as an antiseptic in various healthcare products.

p-Chlorocresol can be found in topical antiseptic solutions, creams, and ointments.
p-Chlorocresol has a history of use in healthcare and personal care products.
p-Chlorocresol is effectiveness as an antimicrobial agent contributed to its inclusion in formulations designed to prevent and treat infections.

p-Chlorocresol is the organic compound with the formula ClC6H4OH.
p-Chlorocresol is a monochlorinated m-cresol.
p-Chlorocresol is a white or colorless solid that is only slightly soluble in water.

p-Chlorocresol can decompose on contact with strong alkalis, evolving heat and fumes that ignite explosively.
p-Chlorocresol is also incompatible with oxidizing agents, copper, and with solutions of calcium chloride, codeine phosphate, diamorphine hydrochloride, papaveretum, and quinine hydrochloride.
p-Chlorocresol is corrosive to metals and forms complex compounds with transition metal ions; discoloration occurs with iron salts.

p-Chlorocresol also exhibits strong sorption or binding tendencies to organic materials such as rubber, certain plastics, and nonionic surfactants.
p-Chlorocresol may be lost from solutions to rubber closures, and in contact with polyethylene may initially be rapidly removed by sorption and then by permeation, the uptake being temperature dependent.
Presoaking of components may reduce losses due to sorption, but not those by permeation.

p-Chlorocresol may also be taken up by polymethylmethacrylate and by cellulose acetate.
Losses to polypropylene or rigid polyvinyl chloride are usually small.
At a concentration of 0.1%, chlorocresol may be completely inactivated in the presence of nonionic surfactants, such as polysorbate 80.

However, other studies have suggested an enhancement of antimicrobial properties in the presence of surfactants.
Bactericidal activity is also reduced, due to binding, by cetomacrogol, methylcellulose, pectin, or cellulose derivatives.
In emulsified or solubilized systems, p-Chlorocresol readily partitions into the oil phase, particularly into vegetable oils, and higher concentrations will be required for efficient preservation.

p-Chlorocresol has been shown to be effective as a bactericide in handwash at 0.2% 2/2 a.s in 60 seconds with 6 ml applied.
p-Chlorocresol is also effective against prions such as scrapie in hamsters.
As an ingredient in cosmetic creams and lotions, p-chlorocresol has a 75% dermal absorption value. Up to 100% dermal absorption may be possible when it is dermally applied to broken skin (eg. for eczema).

p-Chlorocresol, also called 4-Chloro-3-methylphenol, is a white to almost white flake.
The biodegradation of p-Chlorocresol is done in the liver, and then excreted primarily via the kidneys or in smaller amounts through the lungs.
In facultative Thauera sp. strain DO, p-Chlorocresol was degraded aerobically either by dehalogenation followed by catechol degradation pathway, or methyl oxidation to 4-chlorobenzoate.

The exact reaction mechanism in humans is unknown.
p-Chlorocresol is slightly soluble in water(4g/L), easy soluble in organic solvent such as alcohols (96 percent in ethanol), ethers, ketones, etc.

p-Chlorocresol is freely soluble in fatty oils, and dissolves in solutions of alkali hydroxides.
p-Chlorocresol appears as a pinkish to white crystalline solid with a phenolic odor.

Uses:
p-Chlorocresol may be used as an analytical standard for the determination of the analyte in water and soil samples by chromatography techniques.
p-Chlorocresol is used as a preservative in a wide number of topical preparations and is a rare cause of allergic contact dermatitis and CoU, the mechanism of which remains uncertain.
p-Chlorocresol is also used as a preservative in creams and other preparations for external use which contain water.

For use as a disinfectant such as a hand wash, p-Chlorocresol is commonly dissolved in alcohol in combination with other phenols.
p-Chlorocresol is a substituted phenol that functions as a cosmetic biocide preservative in skin care and suntan cosmetic formulations.
For use as a disinfectant such as a hand wash, p-Chlorocresol is commonly dissolved in alcohol in combination with other phenols.

p-Chlorocresol is used as a disinfectant, germicide, preservative, and fungicide.
p-Chlorocresol is a compound used as an antiseptic, disinfectant and fungicide.
p-Chlorocresol is found in creams, topical antiseptics, shampoos, cosmetics and cooling fluids.

p-Chlorocresol is also used as an ingredient in various pharmaceutical preparations.
p-Chlorocresol is used as an antimicrobial preservative in cosmetics and pharmaceutical formulations.
p-Chlorocresol is used as a preservative in a variety of topical preparations, such as corticosteroid creams and moisturizers and in disinfectants and detergents.

p-Chlorocresol is a chlorinated phenol which is used as an antiseptic and preservative.
p-Chlorocresol is mainly used as a disinfectant in the field of poultry, and also can be used as an industrial antimildew agent in the fields of leather, adhesives, coatings, papermaking etc.
p-Chlorocresol may be incorporated into certain industrial cleaning and disinfectant products due to its antimicrobial properties.

These products are designed for use in industrial settings where effective microbial control is essential.
Historically, p-Chlorocresol has been considered for use in oral care products, such as mouthwashes and dental formulations.
p-Chlorocresol is antimicrobial properties could contribute to controlling oral bacteria.

However, alternative antimicrobial agents are often preferred in modern formulations.
p-Chlorocresol has been used in certain veterinary products, including antiseptic solutions and treatments for animals.
p-Chlorocresol is antimicrobial properties can be valuable in veterinary applications.

p-Chlorocresol may have been included in certain cleaning solutions and detergents for its ability to inhibit the growth of microorganisms, contributing to the overall effectiveness of these products.
In some industrial processes involving plastics and polymers, p-Chlorocresol has been considered for its antimicrobial properties to prevent microbial contamination during production and storage.
p-Chlorocresol has been explored for potential use in seed treatment applications, where it could act as a preservative to protect seeds from fungal and bacterial contamination during storage.

p-Chlorocresol has been used in laboratory settings for efficacy testing of antimicrobial agents.
p-Chlorocresol serves as a reference compound to assess the effectiveness of other antimicrobial substances.
Due to regulatory considerations and evolving consumer preferences for milder and more environmentally friendly formulations, the use of p-Chlorocresol has decreased in favor of alternative preservatives and antimicrobial agents in various industries.

Ongoing research in the fields of chemistry and microbiology may lead to new insights into the properties of p-Chlorocresol and its potential applications, or it may contribute to the development of safer and more effective alternatives.
Personal care products, such as antibacterial soap, antibacterial shampoo and health care products is generally used in concentrations up to 0.2% in a variety of preparations except those intended for oral administration or that contact mucous membrane.
p-Chlorocresol is effective against bacteria, spores, molds, and yeasts; it is most active in acidic media.

Preservative efficacy may be reduced in the presence of some other excipients, particularly nonionic surfactants.
p-Chlorocresol is used as a preservative in a variety of topical preparations, such as corticosteroid creams and moisturizers and in disinfectants and detergents.
p-Chlorocresol is used as a disinfectant and preservative found in creams, shampoos, antiseptics, disinfectants, and fungicides.

p-Chlorocresol is a security and efficient anti-mould antiseptic, which can be used in antibacterial hand soap, shampoo and other healthy products.
p-Chlorocresol is mainly used as a disinfectant in the field of poultry, and also can be used as an industrial antimildew agent in the fields of leather, adhesives, coatings, papermaking etc.
p-Chlorocresol is used as an active ingredient in antiseptic solutions, creams, and ointments.

p-Chlorocresol helps prevent and treat infections by inhibiting the growth of bacteria and fungi on the skin.
p-Chlorocresol has been employed as a preservative in some pharmaceutical formulations to prevent the growth of microorganisms and extend the shelf life of the products.
p-Chlorocresol has been used in wood preservation to protect wood from decay and fungal growth. It helps prevent deterioration and extends the lifespan of treated wood.

p-Chlorocresol is frequently used in personal care products, leather, metal machining liquid, concrete, film, gluewater, textile, oiled, paper, etc.
p-Chlorocresol is a security, efficient, anti-mould antiseptic, anti-mildew agent.
p-Chlorocresol is a security, efficient, anti-mould antiseptic, anti-mildew agent.

Particularly effective against putrefactive bacteria and therefore suitable for use in products which are difficult to preserve (e.g. protein-based formulations).
p-Chlorocresol is an activator of ryanodine receptor.
p-Chlorocresol possesses disinfectant and antiseptic properties.

p-Chlorocresol is used in various preparations for skin disinfection and wounds.
In certain dermatological and topical medications, p-Chlorocresol is used for its antimicrobial properties.
p-Chlorocresol can be found in creams, lotions, and other formulations designed for skin application.

While its use in cosmetics has declined in some regions due to regulatory considerations and the desire for alternative preservatives, p-Chlorocresol has been historically used in some cosmetics and personal care products, such as creams, lotions, and soaps.
In the past, p-Chlorocresol has been used as a preservative in certain vaccines to prevent microbial contamination and ensure the integrity of the vaccine during storage.
p-Chlorocresol may be used in certain laboratory applications and industrial processes where antimicrobial properties are required, such as in the production of certain chemical products.

p-Chlorocresol is a compound used as an antiseptic, disinfectant and fungicide.
p-Chlorocresol has been utilized in the textile industry as an antimicrobial agent in the treatment of textiles.
p-Chlorocresol helps prevent the growth of bacteria and fungi on fabrics, contributing to the development of antimicrobial textiles.

p-Chlorocresol has been explored for its potential use as a preservative or antimicrobial agent in certain agricultural formulations.
p-Chlorocresol may be considered in products designed to protect plants or seeds.
In certain water treatment applications, p-Chlorocresol has been investigated for its antimicrobial properties.

p-Chlorocresol may be used to inhibit the growth of bacteria and other microorganisms in water treatment processes.
p-Chlorocresol has found use in the leather industry as a preservative.
p-Chlorocresol helps prevent the growth of bacteria and fungi on leather goods, contributing to the preservation of leather products.

In some formulations in the rubber industry, p-Chlorocresol has been considered for its antimicrobial properties.
p-Chlorocresol may be used to protect rubber products from microbial degradation.
p-Chlorocresol has been used in certain photographic chemicals and processes, where its antimicrobial properties help maintain the stability of solutions used in photography.

p-Chlorocresol may be included in certain cleaning and hygiene products for its antimicrobial properties.
This can contribute to the effectiveness of these products in maintaining cleanliness and preventing microbial contamination.
In some regions and applications, p-Chlorocresol may be considered for use in food contact materials, where its antimicrobial properties could help inhibit the growth of microorganisms.

p-Chlorocresol is found in creams, topical antiseptics, shampoos, cosmetics and cooling fluids.
p-Chlorocresol is also used as an ingredient in various pharmaceutical preparations.

Safety Profile:
p-Chlorocresol is used primarily as a preservative in topical pharmaceutical formulations but has also been used in nebulized solutions and ophthalmic and parenteral preparations.
p-Chlorocresol should not, however, be used in formulations for intrathecal, intracisternal, or peridural injection.
p-Chlorocresol is metabolized by conjugation with glucuronic acid and sulfate and is excreted in the urine, mainly as the conjugate, with little chlorocresol being excreted unchanged.

Although less toxic than phenol, p-Chlorocresol may be irritant to the skin, eyes, and mucous membranes, and has been reported to cause some adverse reactions when used as an excipient.
Poison by intravenous, subcutaneous, and intraperitoneal routes.
Moderately toxic by ingestion.

Incompatible with sodium hydroxide.
When heated to decomposition it emits toxic fumes of Cl and phosgene.
Human exposure to p-Chlorocresol is mostly through body lotions as it is not found naturally in the environment.

Above the critical effect level (21 mg/ kg/ bw/ day), p-chlorocresol exposure may result in a decrease in absolute adrenal gland weights.
In 2021, it was classified as a compound that may constitute a danger to human life or health by the Government of Canada as the margins of exposure of the critical effect level and the estimated levels of exposure were considered inadequate.
Similar to phenol, neurolytic effects have also been reported for p-Chlorocresol.

However, this reaction is rare and may be due to interindividual hypersensitivity.
p-Chlorocresol does not significantly bioaccumulate in organisms due to low Kow and bioconcentration factors.
p-Chlorocresol is not found to be genotoxic or carcinogenic and has been safely used in human medicine for many years.

Health Hazard:
Highly toxic, may be fatal if inhaled, swallowed or absorbed through skin.
Contact with molten substance may cause severe burns to skin and eyes.
Avoid any skin contact.

Effects of contact or inhalation may be delayed.
Fire may produce irritating, corrosive and/or toxic gases.
Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard:
Combustible material: may burn but does not ignite readily.
Containers may explode when heated.
p-Chlorocresol may be transported in a molten form.

Storage:
p-Chlorocresol is stable at room temperature but is volatile in steam.
Aqueous solutions may be sterilized by autoclaving.
On exposure to air and light, aqueous solutions may become yellow colored.

Solutions in oil or glycerin may be sterilized by heating at 1608℃ for 1 hour.
The bulk material should be stored in a well-closed container, protected from light, in a cool, dry place.

Synonyms:
4-Chloro-3-methylphenol
Chlorocresol
59-50-7
4-Chloro-m-cresol
p-Chloro-m-cresol
Parol
Phenol, 4-chloro-3-methyl-
4-Chloro-3-cresol
Ottafact
Baktol
p-Chlorocresol
Candaseptic
2-Chloro-5-hydroxytoluene
Baktolan
Parmetol
Peritonan
Raschit
Aptal
Rasen-Anicon
4-Chloro-5-methylphenol
PCMC
Preventol CMK
Raschit K
p-Chlor-m-cresol
6-Chloro-3-hydroxytoluene
3-METHYL-4-CHLOROPHENOL
2-Chloro-hydroxytoluene
Parachlorometacresol
Chlorocresolum
4-Chloro-3-methyl phenol
m-Cresol, 4-chloro-
NSC 4166
Rcra waste number U039
para-Chloro-meta-cresol
CHEBI:34395
NSC-4166
MFCD00002323
DTXSID4021717
4-Chloro-3-methylphenol-2,6-d2
1-Chloro-2-methyl-4-hydroxybenzene
NCGC00091338-01
Chlorcresolum
Chlorkresolum
Chlorocresolo
Chlorokresolum
Perol
36W53O7109
Chloro-3-cresol
DTXCID601717
Clorocresolo [DCIT]
Clorocresol [Spanish]
Caswell No. 185A
Chlorocresolum [Latin]
Clorocresol
Clorocresolo
Clorocresol [INN-Spanish]
CAS-59-50-7
Chlorocresolum [INN-Latin]
CCRIS 1938
4-chloro-meta-cresol
HSDB 5198
4-Chloro-1-hydroxy-3-methylbenzene
EINECS 200-431-6
4-chloro-3-methyl-phenol
RCRA waste no. U039
EPA Pesticide Chemical Code 064206
BRN 1237629
Lysochlor
Chlorocresol [USAN:INN:NF]
AI3-00075
UNII-36W53O7109
Spectrum_000130
2p7a
4-chlor-3-methylphenol
Chlorocresol (NF/INN)
Spectrum2_000002
Spectrum4_000278
Spectrum5_000705
CHLOROCRESOL [II]
CHLOROCRESOL [MI]
4-chloro-5-methyl-phenol
CHLOROCRESOL [INN]
WLN: QR DG C
CHLOROCRESOL [HSDB]
CHLOROCRESOL [USAN]
EC 200-431-6
SCHEMBL12344
CHLOROCRESOL [MART.]
KBioGR_000776
KBioSS_000590
MLS002152924
BIDD:ER0169
CHLOROCRESOL [WHO-DD]
CHLOROCRESOL [WHO-IP]
DivK1c_000768
Phenol, 4-chloro-5-methyl-
SPECTRUM1500178
SPBio_000003
CHEMBL1230222
4-Chloro-3-methylphenol, 99%
HMS502G10
KBio1_000768
KBio2_000590
KBio2_003158
KBio2_005726
NSC4166
NINDS_000768
P-CHLORO-M-CRESOL [INCI]
HMS1920O03
HMS2091C14
HMS3652F13
HMS3885P09
Pharmakon1600-01500178
CHLOROCRESOL [EP MONOGRAPH]
HY-B1284
Tox21_111116
Tox21_201293
Tox21_300054
BDBM50527069
CCG-39979
HSCI1_000352
NSC756680
s4209
CHLOROCRESOLUM [WHO-IP LATIN]
AKOS000120242
Tox21_111116_1
CS-4678
NSC-756680
Chlorocresol (4-Chloro-3-methylphenol)
IDI1_000768
NCGC00091338-02
NCGC00091338-03
NCGC00091338-04
NCGC00091338-06
NCGC00254021-01
NCGC00258845-01
4-Chloro-3-methylphenol, technical grade
AC-14332
LS-13269
SMR001224524
SBI-0051308.P003
4-Chloro-3-methylphenol, analytical standard
FT-0618220
SW219289-1
EN300-20372
4-Chloro-3-methylphenol, >=98.0% (HPLC)
D03468
AB00051939_02
AB00051939_03
Q302865
SR-05000002033
4-Chloro-3-methylphenol 100 microg/mL in Methanol
Q-200453
SR-05000002033-1
BRD-K89056082-001-03-6
F0001-1543
Z104477910
InChI=1/C7H7ClO/c1-5-4-6(9)2-3-7(5)8/h2-4,9H,1H
43M

PCL-LIQUID
PCL-Liquid is a mixture of branched alkyl fatty acid esters used as a unique emollient providing outstanding skin suppleness.
PCL-Liquid shows high spreading capacity and good skin wetting properties, makes the skin soft, smooth and supple, shows water repellent properties, produces a thin hydrophobic film on the skin which protects from drying out maintains natural water vapor permeability of the skin and counteracts occlusion.
PCL-Liquid is odorless when pure.

CAS: 110-27-0
MF: C17H34O2
MW: 270.45
EINECS: 203-751-4

Synonyms
Isopropyl Myristate, 96% 25GR;IPM 100;IPM-EX;IPM-R;Radia 7730 (IPM);Isopropyl myristate Vetec(TM) reagent grade, 98%;MYRISTIC ACID ISOPROPYL ESTER MINIMU;ISO-PROPYL N-TETRADECANOATE;ISOPROPYL MYRISTATE;110-27-0;Isopropyl tetradecanoate;Estergel;Tetradecanoic acid, 1-methylethyl ester;Bisomel;Isomyst;Promyr;Deltyl Extra;Kesscomir;Tegester;Sinnoester MIP;Crodamol IPM;Plymoutm IPM;Starfol IPM;Unimate IPM;Kessco IPM;Emcol-IM;propan-2-yl tetradecanoate;Wickenol 101;Myristic acid isopropyl ester;Stepan D-50;Emerest 2314;1-Methylethyl tetradecanoate;Deltylextra;JA-FA IPM;Crodamol I.P.M.;Kessco isopropyl myristate;Tetradecanoic acid, isopropyl;FEMA No. 3556;Myristic acid, isopropyl ester;Tetradecanoic acid, isopropyl ester;Caswell No. 511E;Isopropyl myristate [USAN];1-Tridecanecarboxylic acid, isopropyl ester;HSDB 626;NSC 406280;UNII-0RE8K4LNJS;0RE8K4LNJS;EINECS 203-751-4;Estergel (TN);EPA Pesticide Chemical Code 000207;NSC-406280;BRN 1781127;methylethyl tetradecanoate;MFCD00008982;iso-Propyl N-tetradecanoate;DTXSID0026838;CHEBI:90027;EC 203-751-4;Tetradecanoic acid methyethyl ester;1405-98-7;NCGC00164071-01;WE(2:0(1Me)/14:0);isopropylmyristate;MYRISTIC ACID, ISOPROPYL ALCOHOL ESTER;Isopropyl myristate, 98%;TETRADECONOIC ACID, 1-METHYLETHYL ESTER;DTXCID306838;ISOPROPYL MYRISTATE (II);ISOPROPYL MYRISTATE [II];ISOPROPYL MYRISTATE (MART.);ISOPROPYL MYRISTATE [MART.];ISOPROPYL MYRISTATE (USP-RS);ISOPROPYL MYRISTATE [USP-RS];CAS-110-27-0;ISOPROPYL MYRISTATE (EP MONOGRAPH);ISOPROPYL MYRISTATE [EP MONOGRAPH];IPM-EX;Isopropyl myristate; 1-Methylethyl tetradecanoate;IPM-R;tetradecanoic acid 1-methylethyl ester;Deltyextra;Myristic acid-isopropyl ester;Tegosoft M;Isopropyl myristate [USAN:NF];Liponate IPM;Crodamol 1PM;IPM 100;isopropyl-myristate;Lexol IPM;Isopropyltetradecanoate;Radia 7190;Isopropyl myristate (NF);Isopropyl tetradecanoic acid;SCHEMBL2442;Isopropyl myristate, >=98%;CHEMBL207602;ISOPROPYL MYRISTATE [MI];WLN: 13VOY1&1;FEMA 3556;tetradecanoic acid isopropyl ester;ISOPROPYL MYRISTATE [FHFI];ISOPROPYL MYRISTATE [HSDB];ISOPROPYL MYRISTATE [VANDF];Isopropyl myristate, >=90% (GC);Tox21_112080;Tox21_202065;Tox21_303171;ISOPROPYL MYRISTATE [WHO-DD];LMFA0701067;NSC406280;s2428;AKOS015902296;Tox21_112080_1;DB13966;USEPA/OPP Pesticide Code: 000207;NCGC00164071-02;NCGC00164071-03;NCGC00256937-01;NCGC00259614-01;LS-14615;DB-040910;HY124190;CS-0085813;M0481;NS00006471;Isopropyl Myristate Solution. 500mL, Sterile;D02296;F71211

May be synthesized by conventional esterification of PCL-Liquid with myristic acid.
PCL-Liquid is an emollient in cosmetic and pharmaceutical bases.
PCL-Liquid is a fatty acid ester.
PCL-Liquid is an ester of isopropyl alcohol myristic acid.
PCL-Liquid is mainly used as a solubilizer, emulsifier and emollient in cosmetic and topical medicines.
PCL-Liquid also finds applications as a flavoring agent in the food industry.
Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

PCL Liquid is an emollient.
PCL-Liquid helps to protect skin.
PCL-Liquid makes the skin soft, smooth and supple.
PCL-Liquid helps the skin to maintain its natural equilibrium.
PCL-Liquid spreads quickly on skin and has a strong film-forming effect without being occlusive.

Thus, PCL-Liquid does not inhibit the natural skin respiration.
PCL-Liquid does not leave a sticky or greasy skin feeling.
PCL-Liquid maintains the natural moisture content of the skin.
PCL-Liquid mimics the composition of natural preen-gland oil but is of course not animal-derived.
PCL-Liquid offers low variation of viscosity with temperature.
PCL Liquid is particularly suitable for W/O emulsions.

PCL-Liquid Chemical Properties
Melting point: ~3 °C (lit.)
Boiling point: 193 °C/20 mmHg (lit.)
Density: 0.85 g/mL at 25 °C (lit.)
Vapor pressure: Refractive index: n20/D 1.434(lit.)
FEMA: 3556 | ISOPROPYL MYRISTATE
Fp: >230 °F
Storage temp.: 2-8°C
Solubility: <0.05mg/l
Form: Liquid
Specific Gravity: 0.855 (20/4℃)
Color: Clear
Odor: odorless
Water Solubility: Miscible with alcohol. Immiscible with water and glycerol.
Merck: 14,5215
JECFA Number: 311
BRN: 1781127
Stability: Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey: AXISYYRBXTVTFY-UHFFFAOYSA-N
LogP: 7.71
CAS DataBase Reference: 110-27-0(CAS DataBase Reference)
NIST Chemistry Reference: PCL-Liquid (110-27-0)
EPA Substance Registry System: PCL-Liquid (110-27-0)

PCL-Liquid is a colorless and odorless liquid with a faint odor, and miscible with vegetable oil.
PCL-Liquid is not easy to be either hydrolyzed or become rancid.
The refractive index nD20 is 1.435~1.438, and the relative density (20°C) is 0.85~0.86.
PCL-Liquid is used in many applications, including pharma, food and personal care product manufacturing.
PCL-Liquid is a clear, colorless, practically odorless liquid of low viscosity that congeals at about 5°C.
PCL-Liquid consists of esters of propan-2-ol and saturated high molecular weight fatty acids, principally myristic acid.
PCL-Liquid is virtually odorless, very slightly fatty, but not rancid

Content Analysis
Weight 1.5 g sample.
Then PCL-Liquid is determined by the method ester assay (OT-18).
The equivalent factor (e) in the calculation is 135.2.
Or PCL-Liquid is determined by a non-polar column method of gas chromatography (GT-10-4).

Uses
PCL-Liquid is a fatty acid ester which is used as solvent in water-in-oil emulsion, oils and fatty based ointments.
The use of PCL-Liquid is recommended in the Sterility Test chapter of the European, Japanese and United States Pharmacopoeia (EP, 2.6.13, JP, 4.06 and USP, 71) as diluent for oils and oily solutions, as well as for ointments and creams.
Indeed, PCL-Liquid's solvent properties improve the filterability of these samples.
PCL-Liquid is known as a penetration enhancer for topical preparations.
PCL-Liquid is a waterclear, low viscous oily liquid with a very good spreading capacity on the skin.
PCL-Liquid is mainly used in cosmetics as an oilcomponent for emulsions, bath oils and as a solvent for active substances.

PCL-Liquid is an emollient, moisturizer, binder, and skin softener that also assists in product penetration.
An ester of myristic acid, PCL-Liquid is naturally occurring in coconut oil and nutmeg.
Although PCL-Liquid is generally considered comedogenic, some ingredient manufacturers clearly specify non-comedogenicity on their data sheets.
In cosmetic and topical medicinal Preparations where good absorption through the skin is desired.
A jellied PCL-Liquid was marketed as Estergel.

Pharmaceutical Applications
PCL-Liquid is a nongreasy emollient that is absorbed readily by the skin.
PCL-Liquid is used as a component of semisolid bases and as a solvent for many substances applied topically.
Applications in topical pharmaceutical and cosmetic formulations include bath oils; make-up; hair and nail care products; creams; lotions; lip products; shaving products; skin lubricants; deodorants; otic suspensions; and vaginal creams.
For example, PCL-Liquid is a self-emulsifying component of a proposed cold cream formula, which is suitable for use as a vehicle for drugs or dermatological actives; PCL-Liquid is also used cosmetically in stable mixtures of water and glycerol.

PCL-Liquid is used as a penetration enhancer for transdermal formulations, and has been used in conjunction with therapeutic ultrasound and iontophoresis.
PCL-Liquid has been used in a water-oil gel prolonged-release emulsion and in various microemulsions.
Such microemulsions may increase bioavailability in topical and transdermal applications.
PCL-Liquid has also been used in microspheres, and significantly increased the release of drug from etoposide-loaded microspheres.
PCL-Liquid is used in soft adhesives for pressuresensitive adhesive tapes.

Pharmacology
PCL-Liquid is used in pharmaceutical preparations because it improves solubility and increases absorption through the skin.
External uses include a non-irritating iodine preparation for disinfecting the skin and aerosol bactericidal preparations for feminine hygiene use without irritation of the skin and mucous membranes.
Preparations for internal use include oral steroid formulations and anaesthetic injection solutions.
Veterinary medications containing PCL-Liquidinclude oral or parenteral compositions for lungworm infections and a spray formulation for bovine udders to treat mastitis, combat infection and improve the general skin condition.

PCL-Liquid has been found to be an effective repository vehicle for im injection of penicillin in rabbits and for sc administration of oestrogens in ovariectomized rats.
In assays on human forearms, vasoconstrictor activity of ointment preparations containing 0025% betamethasone 17-benzoate in white soft paraffin was increased by the presence of isopropyl myristate.
Donovan, Ohmart & Stoklosa noted that the good solvent properties of PCL-Liquid might increase the therapeutic activity of formulations by the apparent alteration in particle size of the active ingredients, so that further evaluation and clinical study would be necessary before its use in extemporaneous compounding could be recommended.
Studies in which the antifungal activity of paraben esters solubilized by surfactants was decreased by PCL-Liquid indicate that the effectiveness of medicinal substances may be influenced by the presence of surfactants and oily ingredients such as isopropyl myristate.

Production Method
PCL-Liquid is a product of esterification of myristic acid derived from re-steamed coconut coil with isopropyl alcohol.
(1) 200 kg myristic acid and 450 kg isopropyl alcohol were added into the reaction vessel in turn.
After mixing, 360 kg sulfuric acid (98%) was added.
The reaction mixture was heated to reflux for 10 hours.
PCL-Liquid was then recovered, washed with ice water, and neutralized with Na2CO3 aqueous solution (10%).
Under normal pressure, isopropyl alcohol and water were distilled. While under reduced pressure, PCL-Liquid was distilled (185°C/1.0kPa~195°C/2.7kPa).

(2) 90 kg isopropyl alcohol was added into the reaction vessel and then sulfuric acid as catalyst, with 5% of the total amount, was added.
During mixing, 228 kg myristic acid was added slowly.
The mixture was heated to reflux and water was continuously separated.
Until no water was separated, the reaction temperature was reduced and probe was obtained to measure the acid value.
When the acid value reached 1.5 mg KOH/g, the reaction was completed.
Alkali was then added for neutralization.
After the removal of water under reduced pressure, the pressure was further reduced for dealcoholization until the acid value was 0.05~1.0 mg KOH/g.
The final product is then PCL-Liquid.

Production Methods
PCL-Liquid may be prepared either by the esterification of myristic acid with propan-2-ol or by the reaction of myristoyl chloride and propan-2-ol with the aid of a suitable dehydrochlorinating agent.
A high-purity material is also commercially available, produced by enzymatic esterification at low temperature.
PCL-LIQUID 100
PCL-Liquid 100 is a mixture of branched alkyl fatty acid esters used as a unique emollient providing outstanding skin suppleness.
PCL-Liquid 100 shows high spreading capacity and good skin wetting properties which makes the skin soft, smooth and supple and shows water repellent properties.
PCL-Liquid 100 also produces a thin hydrophobic film on the skin which protects from drying out while it maintains natural water vapor permeability of the skin and counteracts occlusion.

CAS: 90411-68-0
MF: C24H48O2
MW: 0
EINECS: 291-445-1

Synonyms
Hexanoic acid, 2-ethyl-, C16-18-alkyl esters;Hexansure, 2-Ethyl-, C16-18-Alkylester;PCL;LIQUID;134647WMX4;Hexadecyl 2-ethylhexanoate;59130-69-7;Cetyl 2-ethylhexanoate;cetyl ethylhexanoate;HEXANOIC ACID, 2-ETHYL-, HEXADECYL ESTER;134647WMX4;EINECS 261-619-1;Schercemol CO;Exceparl HO;Tegosoft C;UNII-134647WMX4;Pelemol 168;90411-68-0;Hest CSO (Salt/Mix);Crodamol CAP (Salt/Mix);EC 261-619-1;Tegosoft liquid (Salt/Mix);SCHEMBL15239;Lanol 1688 (Salt/Mix);HEXADECYL2-ETHYLHEXANOATE;DTXSID20866741;2-Ethylhexanoic acid, cetyl ester;AKOS028108429;DB11349;NS00007021;Hexanoic acid, 2-ethyl-, C16-18-alkyl esters;Q27251471

PCL-Liquid 100 has high resistance to oxidation.
PCL Liquid 100 is an emollient.
This bioinspired ester oils helps to protect your skin.
PCL-Liquid 100 makes the skin soft, smooth and supple.
PCL-Liquid 100 helps the skin to maintain its natural equilibrium.
PCL-Liquid 100 spreads quickly on skin and has a strong film-forming effect without being occlusive.
Thus PCL-Liquid 100 does not inhibit the natural skin respiration.
PCL-Liquid 100 does not leave a sticky or greasy skin feeling.
PCL-Liquid 100 maintains the natural moisture content of the skin.
PCL-Liquid 100 mimics the composition of natural preen-gland oil but is of course not animal-derived.
PCL-Liquid 100 offers a low variation of viscosity with temperature.
PCL Liquid 100 is particularly suitable for W/O emulsions.

PCL-Liquid 100 is the ester of cetearyl alcohol and 2-ethylhexanoic acid and was formerly called cetearyl octanoate.
PCL-Liquid 100 is a transparent, oil-like, water-resistant liquid that protects skin from moisture loss by acting as an emollient.
PCL-Liquid 100, which has a comparable chemical makeup but slightly different properties and safety, should not be confused with this ingredient.
PCL-Liquid 100, commonly known as “seabird feather oil”, can substitute for natural squalane.
PCL-Liquid 100 has good film forming ability, light texture, water-proof and skin-softening, good moisturizers without viscosity.
PCL-Liquid 100 can be used in lipsticks as pigment dispersant, base oil agent, lipstick glossy agent and emollient of cream and lotion, etc.

PCL-Liquid 100 is an ester of cetyl alcohol and 2-ethylhexanoic acid.
PCL-Liquid 100 is present in cosmetic products as a skin conditioning agent and emollient.
PCL-Liquid 100 is a synthetic mixture of fatty acid esters that resembles the preen gland secretion of aquatic birds.
Thus, PCL-Liquid 100 imparts water repelling characteristics to cosmetic formulations.
PCL-Liquid 100 is also used as an agent that improves "spreadability" and "refatting" material for dry skin condition.

PCL-Liquid 100 is a mix of cetyl and stearyl alcohols esters with 2-ethylhexanoic acid, a colorless oil with a faint inherent odor.
PCL-Liquid 100's former designation was Cetearyl Octanoate.

PCL-Liquid 100 is a multifunctional cosmetic oil used in many kinds of skin and hair care preparations.
PCL-Liquid 100 is insoluble in water, freely miscible with vegetable, mineral, and synthetic oils and fats, and dedicated to the oil phase in o/w and w/o emulsions.

PCL-Liquid 100 is a readily emulsifiable oil used as an emollient, spreadability enhancer, and moisturizer.
Closely related to the biological fats of the skin, PCL-Liquid 100 leaves a pleasant after-feel (non-sticky or greasy) and imparts a smooth, glossy appearance to preparations, rendering the skin soft and supple.

By virtue of its branched chain structure, PCL-Liquid 100 is very spreadable.
PCL-Liquid 100 is used as a base oil in the production of a wide variety of cosmetic and pharmaceutical preparations that are easily spread and quickly absorbed by the skin.
Thanks to its good stability against oxidation, PCL-Liquid 100 can be used in sun care applications.
In addition, PCL-Liquid 100 forms a non-occlusive, "breathable" film on the skin that acts as a water-repellant and protects against dehydration.
Thanks to its many beneficial properties, PCL-Liquid 100 is used in many hair, skin, and sun care products and decorative cosmetics.
Toxicological studies have examined the use of PCL-Liquid 100 in cosmetic preparations.
The results obtained did not indicate toxicological hazards when the product was applied in the recommended concentrations for the recommended applications.

Uses
PCL-Liquid 100 works as an emoliient, texture enhancer and a conditioning agent in cosmetics and personal care products.
Skin care: PCL-Liquid 100 smooths and softens the skin.
PCL-Liquid 100 adds a sophisticated spreadability to creams and lotions and is oxygen-stable in addition to its moisturizing qualities.
In leave-on products, PCL-Liquid 100 can be used up to 35% of the time.
Additionally, PCL-Liquid 100 serves as a replacement for whale-derived spermaceti wax.
Numerous cosmetic products, including foundation, facial moisturizers, lipsticks, lip glosses, lip/eye liners, conditioners, and anti-aging products, contain PCL-Liquid 100.
PCL-SOLID
PCL-Solid is a mixture of long-chain fatty acid esters used as an emollient with well-developed consistency giving properties.
PCL-Solid is a colorless wax that melts at skin temperature, has neutral odor, gives emulsions a pleasant consistency and increases their stability.
PCL-Solid creates a soft, pleasant, smooth skin feel, has high levels of refatting potential, also demonstrates strong water repellent properties and forms a hydrophobic film that protects the skin from drying out.

CAS: 24980-41-4
MF: C6H10O2
MW: 114.1424
EINECS: 244-492-7

Synonyms
Ploycarprolactone;Polycaprolactone Standard (Mw 2,000);Polycaprolactone Standard (Mw 4,000);Polycaprolactone Standard (Mw 13,000);Polycaprolactone Standard (Mw 20,000);Polycaprolactone Standard (Mw 40,000);Polycaprolactone Standard (Mw 60,000);Polycaprolactone Standard (Mw 100,000)

PCL Solid is a reliable emollient with valuable caring properties.
PCL-Solid melts slightly above skin temperature.
PCL-Solid gives emulsions a pleasant consistency and helps to increase their stability.
PCL-Solid creates a soft, pleasant and smooth skin feel.
PCL Solid enhances the caring characteristic of formulations.
PCL-Solid is a semi-crystalline polymer, a chemically synthesized biodegradable polymer material, its structural repeating unit has 5 non-polar methylene-CH2 starch, etc.
Substance blending can make completely biodegradable materials.
PCL-Solid is a epsilon-lactone that is oxepane substituted by an oxo group at position 2.

PCL-Solid is a synthetic, semi-crystalline, biodegradable polyester with a melting point of about 60 °C and a glass transition temperature of about −60 °C.
The most common use of PCL-Solid is in the production of speciality polyurethanes. PCL-Solid impart good resistance to water, oil, solvent and chlorine to the polyurethane produced.

PCL-Solid is often used as an additive for resins to improve their processing characteristics and their end use properties (e.g., impact resistance).
Being compatible with a range of other materials, PCL can be mixed with starch to lower its cost and increase biodegradability or PCL-Solid can be added as a polymeric plasticizer to polyvinyl chloride (PVC).
PCL-Solid is also used for splinting, modeling, and as a feedstock for prototyping systems such as fused filament fabrication 3D printers.

PCL-Solid Chemical Properties
Melting point: 60 °C(lit.)
Density: 1.146 g/mL at 25 °C
Tg: -60
Storage temp.: -20°C
Form: pellets
Odor: odorless
InChI: InChI=1S/C6H10O2/c7-6-4-2-1-3-5-8-6/h1-5H2
InChIKey: PAPBSGBWRJIAAV-UHFFFAOYSA-N
EPA Substance Registry System: PCL-Solid (24980-41-4)

Uses
Biodegradable, biocompatible, and bioresorbable polymer composed of ε-caprolactone.
PCL-Solid has been used in the fabrication of research medical devices and research tissue engineering solutions, such as orthopedic or soft tissue fixation devices. Degradation of this material has been thoroughly studied and has been shown to be safely resorbed by the body after implantation.
Modification of molecular weight and polymer composition allows for control of the degradation rate and mechanical stability of the polymer.
Extrusion aid, die lubricant, mold release, pigment and filler dispersion aid and polyester segments in urethanes and block polyesters.

Biomedical applications
PCL-Solid is degraded by hydrolysis of its ester linkages in physiological conditions (such as in the human body) and has therefore received a great deal of attention for use as an implantable biomaterial.
In particular PCL-Solid is especially interesting for the preparation of long term implantable devices, owing to its degradation which is even slower than that of polylactide.

PCL-Solid has been widely used in long-term implants and controlled drug release applications.
However, when PCL-Solid comes to tissue engineering, PCL suffers from some shortcomings such as slow degradation rate, poor mechanical properties, and low cell adhesion.
The incorporation of calcium phosphate-based ceramics and bioactive glasses into PCL-Solid has yielded a class of hybrid biomaterials with remarkably improved mechanical properties, controllable degradation rates, and enhanced bioactivity that are suitable for bone tissue engineering.

PCL-Solid has been approved by the Food and Drug Administration (FDA) in specific applications used in the human body as (for example) a drug delivery device, suture, or adhesion barrier.
PCL-Solid is used in the rapidly growing field of human esthetics following the recent introduction of a PCL-based microsphere dermal filler belonging to the collagen stimulator class (Ellansé).

Through the stimulation of collagen production, PCL-based products are able to correct facial ageing signs such as volume loss and contour laxity, providing an immediate and long-lasting natural effect.
PCL-Solid is being investigated as a scaffold for tissue repair by tissue engineering, GBR membrane.
PCL-Solid has been used as the hydrophobic block of amphiphilic synthetic block copolymers used to form the vesicle membrane of polymersomes.
A variety of drugs have been encapsulated within PCL-Solid beads for controlled release and targeted drug delivery.

In dentistry (as the composite named Resilon), PCL-Solid is used as a component of "night guards" (dental splints) and in root canal filling.
PCL-Solid performs like gutta-percha, has similar handling properties, and for re-treatment purposes may be softened with heat, or dissolved with solvents like chloroform.
Similar to gutta-percha, there are master cones in all ISO sizes and accessory cones in different sizes and taper available.
The major difference between the polycaprolactone-based root canal filling material (Resilon and Real Seal) and gutta-percha is that the PCL-Solid is biodegradable, whereas gutta-percha is not.
There is a lack of consensus in the expert dental community as to whether a biodegradable root canal filling material, such as Resilon or Real Seal is desirable.

Properties and Applications
PCL-Solid is a biodegradable, semicrystalline polyester for use in tissue engineering and drug delivery research applications.
Due to the increased length of the aliphatic chain, PCL-Solid degrades significantly slower than other common biodegradable polymers, such as polylactide.
PCL-Solid features a low melting point (55-60 °C), making it ideal for thermal processing and increasing its use in novel applications such as 3D bioprinting.
In addition to its favorable thermal properties, PCL-Solid also features high solubility in organic solvent allowing for a multitude of other processing options.
PCL-Solidfeatures low residual water, monomer, and catalyst (tin) making it an ideal choice for use in tissue engineering and 3D bioprinting research.

Synthesis
PCL-Solid is prepared by ring opening polymerization of ε-caprolactone using a catalyst such as stannous octoate.
A wide range of catalysts can be used for the ring opening polymerization of caprolactone.
PCMC
Chlorocresol; 3-Methyl-4-chlorophenol; 4-Chloro-3-methyl phenol; Parachlorometacresol; p-Chloro-m-cresol; 2-Chloro-5-hydroxytoluene; 2-Chloro-hydroxytoluene; 4-Chloro-1-hydroxy-3-methylbenzene; 4-Chloro-3-cresol; 4-Chloro-3-methylphenol; 4-Chloro-5-methylphenol; 4-Chloro-m-cresol; 6-Chloro-3-hydroxytoluene; 6-Chloro-m-cresol; Chlorkresolum; Chloro-3-cresol; Chlorocresol; Chlorocresolo; Chlorocresolum; Clorocresolo; Parachlorometacresol; Parmetol; Parol; Peritonan; Perol; p-Chlor-m-cresol; p-Chloro-m-cresol; p-Chlorocresol CAS NO:59-50-7
PCMX
PCMX Chloroxylenol, also known as para-chloro-meta-xylenol (PCMX), is an antiseptic and disinfectant which is used for skin disinfection, and together with alcohol for cleaning surgical instruments.[2] PCMX is also used within a number of household disinfectants and wound cleaners.[3] PCMX is thought to act by disrupting microbial cell walls and inactivating cellular enzymes, and is less effective than some other available agents. PCMX is available as a liquid. History of PCMX PCMX was first made in 1927. It is on the World Health Organization's List of Essential Medicines.[8] It is sold in a number of formulations and under a number of brand names, including Dettol. Soon after it was created parachlorometaxylenol was then called PCMX, but this was thought to be a poor name and it was renamed Dettol. Then in 1932 it was marketed in Britain and in India. It had a white on green bottle with a white sword depicted. PCMX is sold, in the same style bottle, in Argentina and Uruguay to this day. Properties of PCMX Side effects are generally few but can include skin irritation.[2][5] It may be used mixed with water or alcohol. PCMX is most effective against gram-positive bacteria.[2] It works by disruption of the cell wall and stopping the function of enzymes. Uses of PCMX PCMX is used in hospitals and households for disinfection and sanitation. It is also commonly used in antibacterial soaps, wound-cleansing applications and household antiseptics such as Dettol liquid (to which it contributes its distinctive odor), cream and ointments.[13]Following independent laboratory testing specific Dettol products have demonstrated effectiveness against the Covid-19 virus (SARS-CoV-2) when used in accordance with the directions for use. Side effects of PCMX PCMX is not significantly toxic to humans, is practically non-toxic to birds, and is moderately toxic to freshwater invertebrates. It is highly toxic to fish, cats, and some amphibians and should not be used around them. PCMX is a mild skin irritant and may trigger allergic reactions in some individuals. Humans Excessive exposure to PCMX has the potential for causing death. It can be poisonous when swallowed and even when it is unintentionally inhaled. A medical study in Hong Kong which analyzed 177 cases of Dettol ingestion that resulted in emergency department treatment (95% of which were intentional), concluded that "Dettol poisoning resulted in serious complications in 7% of patients, including death." Animals PCMX is toxic to many animals, especially cats. Phenolic compounds are of particular concern because cats are unable to fully metabolize them. A cat may swallow the product by licking its paws after they have come into contact with it. In Australia, PCMX spray has been shown to be lethal to cane toads, an invasive species that was introduced from Hawaii as a result of bad judgment in 1935. It had been hoped that the amphibian would control the cane beetle but it became highly destructive within the ecosystem. Spraying the disinfectant at close range has been shown to cause rapid death to toads. PCMX is not known whether the toxins are persistent or whether they harm other Australian flora and fauna. Owing to concerns over potential harm to other Australian wildlife species, the use of PCMX as an agent for pest control was banned in Western Australia by the Department of Environment and Conservation in 2011. Society and culture A number of brand names are available. PCMX is the active ingredient in Dettol. PCMX comprises 4.8% of Dettol's total admixture,[19] with the rest made up by pine oil, isopropanol, castor oil, soap and water. Chloroxylenol (PCMX) also called 4-Chloro-3, 5-dimethylphenol, is a white crystal. PCMX is a secure, high-efficient, broad spectrum and low-toxic antiseptic. PCMX has large potency to Gram-positive, Gram-negative, epiphyte and mildew approved by FDA . PCMX has good chemical stability and doesn’t lose the activity in normal storage conditions. Solubility in water is 0.03 wt%, freely soluble in organic solvent such as alcohols, ethers, polyglycols, etc. and solutions of alkali hydroxides frequently used in personal clean care products. This product (PCMX) is low-poison antibacterial, frequently used in personal care products such as hand - cleaning detergent, soap, dandruff control shampoo and healthy products, etc. Common dosage in lotion as follows: 0.5~1wt% in liquid detergent, 1wt% in antibacterial handing detergent, 4.5~5 wt% in disinfectant. What’s more, PCMX has been used in other fields such as glue, painting, textile, pulp, etc. This study examines the bactericidal and fungicidal efficiency of parachlorometaxylenol (PCMX) and its active ingredient, chlorxylenol at 10% and 20% concentrations, on four microbial isolates from abattoirs' (slaughter houses) floors in an open environment in Port Harcourt metropolis, Rivers State Nigeria. The study was carried out between the months of January 2005 and June 2006. Mixed culture of Vibrio species, Salmonella sp, Campylobacter sp and Candida albicans isolated from five different abattoirs: Agip, Trans -Amadi, Woji, Rumuodara and Rumuokoro: were used as test bacteria and fungi respectively, using agar diffusion and tranditional plate count methods. The four microbial isolates were exposed to parachlorometaxylenol (PCMX) and chlorxylenol after the addition of quenching agent (QAC), at time interval starting from Omin, lOmin, 20min, 30min, 40,min, 50min,and 60min. Analysis of Variance (ANOVA) was calculated on the resistance and the susceptibility of these four isolates to the test disinfectants, the results showed that there was no significant difference in the test disinfectants effectiveness on these test organisms. The findings showed that Vibrio, Salmonella and Campylobacter were more sensitive to parachlorometaxylenol (PCMX) also called Dettol, while Candida albicans was more sensitive to Chlorxylenol. Also observed from this work is candidiasis infection through cross-contamination can be taken care of in the body of its victim by washing in 10% chloroxylenol. At ambient temperature, a 25% solution of PCMX in isopropanol is not corrosive to stainless steel or aluminum. Brass is slightly affected as is mild steel. Mild steel is slightly affected by isopropanol alone. PCMX is stable when exposed to sunlight and humidity from ambient storage over 24 hours. It is also stable at elevated temperatures (54 °C). Choroxylenol is hydrolytically stable. Drug Indication of PCMX The predominant medical applications for which PCMX is formally indicated for therapeutic use is as an application to the skin for use in cuts, bites, stings, abrasions, and for use as antiseptic hand cleaner. PCMX is a substituted phenol which has been widely used for many years as an ingredient of antiseptic and disinfectant products intended for external use [L1999]. PCMX is known to be bactericidal in low concentration to a wide range of Gram positive and Gram negative bacteria. Absorption No PCMX was detected in the blood following the dermal administration of 2 g of p-PCMX in an ethanol/olive oil vehicle in human subjects. After a dose of 5 g, only traces were found, after 8 g, 1 mg % (1 mg/dL) was found in the blood after 3 hours, and 4 mg % (4 mg/dL) after 24 hours [A32349]. After a dose of 20 g, 4 mg % (4 mg/dL) was measured after half an hour, and 1 mg % (1 mg/dL) was present at 72 hours [A32349]. For antiseptic purposes, PCMX is considered to be well-absorbed when applied to the skin. Volume of Distribution The only data available regarding the volume of distribution of PCMX is the mean Vss of 22.45 L determined after 200 mg intravenous single dose of PCMX was administered to healthy mongrel dog subjects. Clearance The only data available regarding the clearance of PCMX is the mean clearance rate of 13.76 L/hr following a 200 mg intravenous single dose of the substance into healthy mongrel dog subjects [L1989, L1993]. Moreover, in another study, when 8 g of PCMX was administered dermal on a human subject in an alcohol/glycerin vehicle, 11% was excreted in 48 hours. The pharmacokinetic and metabolic profile of p-chloro-m-xylenol (PCMX) was studied in healthy mongrel dogs after intravenous and oral administration of single doses of 200 and 2000 mg of PCMX, respectively. ... The mean half-life and mean residence time were 1.84 and 1.69 hr. respectively. The apparent volume of distribution at steady state was estimated to be 22.4 liters, and the plasma clearance was 14.6 liters/hr. The bioavailability of PCMX was 21%. ... PCMX's metabolite data show that a presystemic elimination process (first-pass effect) is also occurring. PCMX plasma concentrations after intravenous administration of 500-, 200-, and 100-mg doses were found to be proportional to the dose given. Metabolism/Metabolites Certain animal studies have shown that following dermal application of PCMX, that the absorption was rapid with a Cmax = 1-2 hours, and that the administered substance was excreted via the kidney with almost complete elimination within 24 hours. The primary metabolites discovered in the excreted urine were glucuronides and sulfates [L1992]. Some PCMX monographs liken its pharmacokinetic profile to that of another antiseptic - triclosan - which is rapidly excreted in the urine also as a glucuronide metabolite, as observed in the human model. Moreover, In one human subject administered 5 mg intragluteally, 14% was excreted with glucuronic acid and 17% with sulfuric acid at 3 days. Any PCMX absorbed into the body is likely extensively metabolized by the liver and rapidly excreted, mainly in the urine, as sulphate and glucuronide conjugates. One study estimated the mean terminal half-life and mean residence time after a 200 mg intravenous single dose of PCMX in healthy mongrel dog subjects to be 1.7 and 1.69 hours, respectively. Alternatively, some product monographs liken PCMX to a similar liquid antiseptic, triclosan, whose calculated urinary excretion half-life in man is approximately 10 hours. As a phenol antiseptic, it is believed that the hydroxyl -OH groups of the PCMX molecule binds to certain proteins on the cell membrane of bacteria, and disrupts the membrane so as to allow the contents of the bacterial cell to leak out [A1351]. This allows PCMX to enter the bacterial cell to bind further with more proteins and enzymes to disable the cell's functioning [A1351]. At particularly high concentrations of PCMX, the protein and nucleic acid content of targeted bacterial cells become coagulated and cease to function, leading to rapid cell death. Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. PCMX is included on this list. Section 4(g)(2)(A) of FIFRA calls for the Agency to determine, after submission of relevant data concerning an active ingredient, whether products containing the active ingredients are eligible for reregistration. The Agency has previously identified and required the submission of the generic (i.e. active ingredient specific) data required to support reregistration of products containing PCMX active ingredients. The Agency has completed its review of these generic data, and has determined that the data are sufficient to support reregistration of all products containing PCMX. Drug products containing certain active ingredients offered over-the-counter (OTC) for certain uses. A number of active ingredients have been present in OTC drug products for various uses, as described below. However, based on evidence currently available, there are inadequate data to establish general recognition of the safety and effectiveness of these ingredients for the specified uses: PCMX is included in topical acne drug products. Toxicity Summary of PCMX As PCMX is predominantly employed as an active ingredient in various liquids or creams as cleaners, disinfectants, or antiseptics that are generally designed to be used topically, it is widely accepted that the use of such liquids - when used appropriately - is unlikely to present a sufficient volume that could be ingested to cause any medical problems [L1992]. In the event of accidental eye contact, was with Luke warm water [L1992]. PCMX is known to have a low systemic toxicity, even at dosage levels many times higher that those likely to be absorbed during normal usage of the agent. Environmental Fate/Exposure Summary of PCMX PCMX's production and use as an antibacterial, germicide, antiseptic and in mildew prevention may result in its release to the environment through various waste streams. If released to air, a vapor pressure of 0.1 mm Hg at 20 °C indicates PCMX will exist solely as a vapor in the atmosphere. Vapor-phase PCMX will be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 5.8 hours. PCMX does not absorb at wavelengths >290 nm and has been reported to be stable to sunlight for up to 24 hours. If released to soil, PCMX is expected to have low mobility based upon an estimated Koc of 1,400. Volatilization from moist soil surfaces is not expected to be an important fate process based upon an estimated Henry's Law constant of 5.1X10-7 atm-cu m/mole. PCMX is not expected to volatilize from dry soil surfaces based upon its vapor pressure. Volatilization from water surfaces is expected to be an important fate process based upon this compound's estimated Henry's Law constant. Estimated volatilization half-lives for a model river and model lake are 10 hours and 9 days, respectively. Degradation of PCMX appears to be slower than other phenol derivatives. Studies in sewage showed 80-95% of the original compound remaining after 2 days and 60-70% remaining after 7 days. This is consistent with other studies that showed less than 40% degradation in activated sludge over 7 days. If released into water, PCMX is not expected to adsorb to suspended solids and sediment based upon the estimated Koc. An estimated BCF of 66 suggests the potential for bioconcentration in aquatic organisms is moderate. Hydrolysis is not expected to be an important environmental fate process since this compound lacks functional groups that hydrolyze under environmental conditions. Occupational exposure to PCMX may occur through inhalation and dermal contact with this compound at workplaces where PCMX is produced or used. The most likely route of exposure to the general population is through dermal contact when using soaps or cleaning products that contain PCMX as an antibacterial. A smaller population may be exposed to PCMX when taking medications that contain PCMX as an active ingredient. PCMX's production and use as an antibacterial, germicide, antiseptic and in mildew prevention(1) may result in its release to the environment through various waste streams(SRC). TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 1,400(SRC), determined from a log Kow of 3.27(2) and a regression-derived equation(3), indicates that PCMX is expected to have low mobility in soil(SRC). Volatilization of PCMX from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 5.1X10-7 atm-cu m/mol(SRC), derived using a fragment constant estimation method(4). PCMX is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(4). Degradation of PCMX appears to be slower than other phenol derivatives(5,6). Studies in sewage showed 95-80% of the original compound remaining after 2 days and 60-70% remaining after 7 days(5). This is consistent with other studies that showed less than 40% degradation in activated sludge over 7 days(6). ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), PCMX, which has an estimated vapor pressure of 1.8X10-3 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase PCMX is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 6 hours(SRC), calculated from its rate constant of 6.7X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). PCMX does not contain chromophores that absorb at wavelengths >290 nm(4) and has been reported to be stable to sunlight for up 24 hours(5). The rate constant for the vapor-phase reaction of PCMX with photochemically-produced hydroxyl radicals has been estimated as 6.7X10-11 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(1). This corresponds to an atmospheric half-life of about 5.8 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1). PCMX is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions(2). PCMX does not absorb at wavelengths >290 nm(3) and has been reported to be stable to sunlight for up to 24 hours(4). An estimated BCF of 66 was calculated for PCMX(SRC), using a log Kow of 3.27(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is moderate(SRC), provided the compound is not metabolized by the organism(SRC). The Koc of PCMX is estimated as 1,400(SRC), using a log Kow of 3.27(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that PCMX is expected to have low mobility in soil. The Henry's Law constant for PCMX is estimated as 5.1X10-7 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that PCMX is expected to be essentially nonvolatile from moist soil and water surfaces(2). PCMX is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 1.8X10-3 mm Hg(SRC), determined from a fragment constant method(3). Occupational exposure to PCMX may occur through inhalation and dermal contact with this compound at workplaces where PCMX is produced or used(SRC). The most likely route of exposure to the general population is through dermal contact when using soaps or cleaning products that contain PCMX as an antibacterial(SRC). A smaller population may be exposed to PCMX when taking medications that contain PCMX as an active ingredient(1). Because of the broad-spectrum antimicrobial activity of para-chlorometa- xylenol (PCMX) and the need for additional topical agents for bacterial control of the burn wound, PCMX was tested in an in vitro topical antimicrobial susceptibility well assay system. For testing, data from 50 strains of Staphvlococcus aureus and 100 strains of various gram-negative micro-organisms were isolated from wounds of acute burn patients. Results showed that burns colonized by organisms other than P. aeruginosa could be treated with PCMX as a single agent, whereas burn wounds not so colonized could be treated with mixtures of PCMX and an antimicrobial that has anli-Pseudomonas activity. Alternatively, PCMX could be mixed with antimicrobials against which organisms show random resistance and thus expand their spectrum of activity. Therefore, further testing and development of PCMX as a topical antimicrobial preparation seems warranted. Para-Chloro-Meta-Xylenol (PCMX) is an antiseptic and disinfectant. Used for skin disinfection and cleaning surgical instruments. It is also used within a number of household disinfectants and wound cleaners. PCMX is an antimicrobial chemical compound used as a preservative to control bacteria, algae, and fungi in adhesives, emulsions, paints, cooling fluids, glue, cosmetics, hygiene products such as hair conditioners and deodorants, topical medications, urinary antiseptics and metal working fluids. Liquid PCMX solutions are used for cleaning and disinfecting wounds, abrasions and abscesses while creams are used for cuts, scratches, insect bites, and burns. Powders are used to treat problems of the feet and skin inflammations. Uses of PCMX: Preservative in cooling fluids, creams, topical and urinary antiseptics. Chloroxylenol (PCMX) acts against a wide range of bacteria. Liquids are used for the cleaning and disinfecting of wounds and abrasions as well as abscesses. The creams are used for cuts, scratches, insect bites, burns and similar problems. Powders can be used to treat tinea problems of the feet and skin inflammations. Also in pharmaceutical products, hair conditioners, toilet and deodorants, soaps, electrocardiogram paste, etc. Chloroxylenol, or para-chloro-meta-xylenol (PCMX), is an antiseptic and disinfectant agent used for skin disinfection and surgical instruments. PCMX is found in antibacterial soaps, wound-cleansing applications, and household antiseptics. The halophenol is shown to be most effective against Gram positive bacteria where it disrupts the cell wall due to its phenolic nature 1. PCMX is on the World Health Organization's List of Essential Medicines. PCMX is a substituted phenol which has been widely used for many years as an ingredient of antiseptic and disinfectant products intended for external use. It is known to be bactericidal in low concentration to a wide range of Gram positive and Gram negative bacteria. As a phenol antiseptic, it is believed that the hydroxyl -OH groups of the PCMX molecule binds to certain proteins on the cell membrane of bacteria, and disrupts the membrane so as to allow the contents of the bacterial cell to leak out. This allows PCMX to enter the bacterial cell to bind further with more proteins and enzymes to disable the cell's functioning. At particularly high concentrations of PCMX, the protein and nucleic acid content of targeted bacterial cells become coagulated and cease to function, leading to rapid cell death. Volume of distribution The only data available regarding the volume of distribution of PCMX is the mean Vss of 22.45 L determined after 200 mg intravenous single dose of PCMX was administered to healthy mongrel dog subjects 6,8. Protein binding One study determined the protein binding of PCMX to be approximately 85.2% +/- 2.32% for serum albumin and 89.8% +/- 2.99% for whole human serum. Metabolism Certain animal studies have shown that following dermal application of PCMX, that the absorption was rapid with a Cmax = 1-2 hours, and that the administered substance was excreted via the kidney with almost complete elimination within 24 hours. The primary metabolites discovered in the excreted urine were glucuronides and sulfates. Some PCMX monographs liken its pharmacokinetic profile to that of another antiseptic - triclosan - which is rapidly excreted in the urine also as a glucuronide metabolite, as observed in the human model. Moreover, In one human subject administered 5 mg intragluteally, 14% was excreted with glucuronic acid and 17% with sulfuric acid at 3 days 4. Any PCMX absorbed into the body is likely extensively metabolized by the liver and rapidly excreted, mainly in the urine, as sulphate and glucuronide conjugates. Route of elimination of PCMX The major route of excretion is likely in urine 8,7, although some amounts may be found in bile and traces in exhaled air. Half-life One study estimated the mean terminal half-life and mean residence time after a 200 mg intravenous single dose of PCMX in healthy mongrel dog subjects to be 1.7 and 1.69 hours, respectively 6,8. Alternatively, some product monographs liken PCMX to a similar liquid antiseptic, triclosan, whose calculated urinary excretion half-life in man is approximately 10 hours. Clearance of PCMX The only data available regarding the clearance of PCMX is the mean clearance rate of 13.76 L/hr following a 200 mg intravenous single dose of the substance into healthy mongrel dog subjects. Moreover, in another study, when 8 g of PCMX was administered dermal on a human subject in an alcohol/glycerin vehicle, 11% was excreted in 48 hours. Toxicity of PCMX As PCMX is predominantly employed as an active ingredient in various liquids or creams as cleaners, disinfectants, or antiseptics that are generally designed to be used topically, it is widely accepted that the use of such liquids - when used appropriately - is unlikely to present a sufficient volume that could be ingested to cause any medical problems 7. In the event of accidental eye contact, was with Luke warm water 7. PCMX is known to have a low systemic toxicity, even at dosage levels many times higher that those likely to be absorbed during normal usage of the agent. Drug overdose There have been many cases of intoxication with oral PCMX liquid, a widespread household disinfectant that contains PCMX 4.8%, pine oil, and isopropyl alcohol [4–8]. PCMX was involved in 10% of hospital admissions related to self-poisoning in Hong Kong. In a retrospective study of 67 cases, serious complications were relatively common (8%) and these included aspiration of PCMX with gastric contents, resulting in pneumonia, cardiopulmonary arrest, bronchospasm, adult respiratory distress syndrome, and severe laryngeal edema with upper airway obstruction. Of 89 patients, five developed minor hematemesis, in the form of coffee-colored or blood-stained vomitus [6]. One patient had a gastroscopy performed on the day after admission, which showed signs of chemical burns in the esophagus and stomach. Gastroscopy in another patient on day 11, done to rule out an esophageal stricture, showed no abnormality. All patients with hematemesis recovered completely. The authors suggest that upper gastrointestinal hemorrhage after PCMX ingestion tends to be mild and self-limiting. Gastroscopy, which may increase the risk of aspiration in patients with impaired consciousness, is not required unless other causes of gastrointestinal bleeding are suspected. Furthermore, PCMX poisoning can be associated with an increased risk of aspiration, possibly caused by the use of gastrointestinal lavage in 88% of the patients and vomiting in 62%. Of 121 patients who ingested PCMX 200–500 ml, three developed renal impairment, as evidenced by raised plasma urea and creatinine [7]. Two of these patients also had serious complications, including aspiration leading to pneumonia and adult respiratory distress syndrome; one died. Renal impairment only appears to be observed when relatively large amounts of PCMX are ingested [7]. PCMX is used in cosmetic products as an antimicrobial at concentrations up to 5.0 percent. It is absorbed through the human skin and gastrointestinal tract. Following oral ingestion by a human of a product formulated with PCMX, both free and conjugated PCMX were detected in the urine. PCMX at 100 percent concentration was a moderate irritant to the rabbit eye, whereas a 0.1 percent aqueous PCMX solution was a nonirritant to rabbit skin. PCMX was nonmutagenic in the Salmonella mutagenesis assay, both with and without metabolic activation. No carcinogenicity or adequate teratogenicity studies have been reported. In clinical studies, formulations containing up to 1 .O percent Chloroxyleno1 were nonsensitizing and essentially nonirritating to the skin. The incidence of skin sensitization among 1752 dermatitis patients exposed to 1 .O percent PCMX was less than 1 .O percent. On the basis of the available information included in this report, it is concluded that PCMX is safe as a cosmetic ingredient in the present practices of use.
PDMS SILICONE OIL 350CST
PDMS Silicone Oil 350cSt is a kind of oily linear polysiloxane produced from the hydrolysis and poly-condensation of chlorotrimethylsilane, ethyl chlorosilane, and phenyl chlorosilane containing mono-functional group and bifunctional group.
The commonly called PDMS Silicone Oil 350cSt means the polydimethylsiloxane and polymethyl phenyl siloxane.
PDMS Silicone Oil 350cSt is a kind of colorless, odorless, non-toxic, transparent, non-volatile liquid with non-corrosive effect on metal, low freezing point and good anti-water property and moisture resistance, low surface tension and being capable of being resistant to dilute acids and bases and has wide application in various national economy departments.

CAS: 63148-62-9
MF: C6H18OSi2
MW: 162.38
EINECS: 613-156-5

Synonyms
DIETHYL ETHER RECTIFIED;ETHYL ACETATE PESTINORM SUPRA TRACE;SILICONE FLUID;2,2,4,4-TETRAMETHYL-3-OXA-2,4-DISILAPENTANE;BIS(TRIMETHYLSILYL)ETHER;Hexamethyloxy disilane;HMDO;dimethylsilicone fluid;OCTAMETHYLTRISILOXANE;107-51-7;Trisiloxane, octamethyl-;63148-62-9;1,1,1,3,3,5,5,5-Octamethyltrisiloxane;dimethyl-bis(trimethylsilyloxy)silane;Dimeticone;Dimethicone 350;Pentamethyl(trimethylsilyloxy)disiloxane
;Dimethylbis(trimethylsiloxy)silane;9G1ZW13R0G;CHEBI:9147;DTXSID9040710;Dimethicones
;Trisiloxane, 1,1,1,3,3,5,5,5-octamethyl-;MFCD00084411;MFCD00148360;CCRIS 3198;EINECS 203-497-4;dimeticonum;UNII-9G1ZW13R0G;Dimeticona;FRD 20;Ctamethyltrisiloxane;MFCD00008264;Pentamethyl(trimethylsiloxy)disiloxane;octamethyl-trisiloxane;dimethicone macromolecule;VOLASIL DM-1;TRISILOXANE [INCI];EC 203-497-4;Octamethyltrisiloxane, 98%;OS 20 (SILOXANE);SCHEMBL23459;TRISILOXANE, OCTAMETHYL;Dow Corning High-Vacuum Grease;CHEMBL2142985;DTXCID7020710;CHEBI:31498;CXQXSVUQTKDNFP-UHFFFAOYSA-;KF 96A1;OCTAMETHYLTRISILOXANE [MI];dimethylbis(trimethylsiloxy)siliane;Dimethylbis(trimethylsilyloxy)silane;[(CH3)3SiO]2Si(CH3)2;Tox21_301002;CO9816;MFCD00134211;MFCD00165850;Silane, dimethylbis(trimethylsiloxy)-;AKOS015840180;FS-4459;NCGC00164100-01;NCGC00164100-02
;NCGC00254904-01;CAS-107-51-7;NS00041459;O0257;O9816;C07261;D91850;S12475;viscosity 500 inverted exclamation markA30mPa.s;A801717;J-001906;Q2013799;2,2,4,4,6,6-hexamethyl-3,5-dioxa-2,4,6-trisilaheptane;InChI=1/C8H24O2Si3/c1-11(2,3)9-13(7,8)10-12(4,5)6/h1-8H3;28349-86-2

The viscosity of the PDMS Silicone Oil 350cSt has small changes with temperature.
At-60~250 °C, PDMS Silicone Oil 350cSt can be used as a lubricant agent for sextant, electromotor, shells aiming system and shipborne radar devices.
When being mixed with thickener such as carbon black and lithium stearate, PDMS Silicone Oil 350cSt can be used for preparation of viscous grease for being applied to vacuum or high temperature sealing systems and the sealing of vacuum cocks, bushings, and valve.
PDMS Silicone Oil 350cSt will not be cured by high compression with a relative high compressibility and can be used as liquid springs of aircraft and used for eliminating flutter in the buffer, shock absorption system to maintain the stability of the gauge pointer in aircraft cabin and damping of damper device.

Because of its non-corrosiveness on metal and long lifespan, it is widely used as hydraulic pressure fluid in various kinds of delivery systems such as being the hydraulic pressure fluid of aircraft landing gear, flaps, doors, and speed brakes; Because of its small density, low viscosity, PDMS Silicone Oil 350cSt can decrease the weight of the hydraulic pressure systems of the aircraft system by 45% compared with the mineral oil system.
PDMS Silicone Oil 350cSt is heat resistant and can be used as the heat transfer medium of-50~250 ℃; it does not absorb moisture and has excellent electrical insulation and can resist high temperature to be used as a dielectric liquid for being applied to the capacitors and the miniature transformer of encapsulating and impregnating.
PDMS Silicone Oil 350cSt is permeable to visible light and can be coated to the lens and optical glass to improve the light transmission properties; its being coated to the motion picture film can reduce the friction and extend the lifespan of the film.

PDMS Silicone Oil 350cSt has a good water resistance and can be used for processing wool, rayon, nylon, cotton fabric and can be used for making waterproof fabric; PDMS Silicone Oil 350cSt has a low surface tension and can be used for plastic and rubber mold releasing agents; in the food and textile industry, PDMS Silicone Oil 350cSt can be used in defoamers.
PDMS Silicone Oil 350cSt is non-toxic with physiologically inertia and can be used for the treatment of flatulence and can also play a role of skin care when added to cosmetics.
Any of a large group of siloxane polymers based on a structure consisting of alternate silicon and oxygen atoms with various organic radicals attached to the silicon:
PDMS Silicone Oil 350cSt is low viscosity liquid polymerized siloxanes with organic side chains.

A high quality of silicone oil which is clear liquid.
PDMS Silicone Oil 350cSt's viscosity shows very little change with temperature variation.
PDMS Silicone Oil 350cSt exhibits minimum of change among all types of silicone fluids.
Outstanding resistance to high and low temperature extremes, maintenance of flexibility over a wide temperature range are its unique properties.
With a flash point of 315oC PDMS Silicone Oil 350cSt is ideal for use as an oil bath up to 230oC
PDMS Silicone Oil 350cSt shows high resistance to breakdown by mechanical shearing.
The low change in viscosity with temperature and excellent heat and cold resistance makes it an ideal lubricant.
PDMS Silicone Oil 350cSt is, therefore, widely used in gear wheels, bearings and brushes.
PDMS Silicone Oil 350cSt exhibits excellent dielectric properties, which are maintained for prolonged periods of time even under varying operating conditions.
PDMS Silicone Oil 350cSt is used in personal care products as it is a good foam builder, PDMS Silicone Oil 350cSt imparts soft silky feel to the hair, ensures smooth wet shaving foams and is non-irritant to skin.

PDMS Silicone Oil 350cSt Chemical Properties
Melting point: −59 °C(lit.)
Boiling point: 101 °C(lit.)
Density: 0.963 g/mL at 25 °C
Vapor density: >1 (vs air)
Vapor pressure: Refractive index: n20/D 1.377(lit.)
Fp: >270 °C (518 °F)
Storage temp.: 2-8°C
Solubility: Chloroform (Slightly), Ethyl Acetate (Sparingly), Toluene (Sparingly)
Form: Oily Liquid
Specific Gravity: 0.853
Color: Clear colorless
Odor: Odorless
Water Solubility: PRACTICALLY INSOLUBLE
Merck: 14,8495
Dielectric constant: 2.7(Ambient)
Stability: Stable. Incompatible with strong oxidizing agents.
EPA Substance Registry System: PDMS Silicone Oil 350cSt (63148-62-9)

PDMS Silicone Oil 350cSt is milk-white viscous liquid and is non-volatile and odorless.
PDMS Silicone Oil 350cSt has a relative density of O.98~1.02.
PDMS Silicone Oil 350cSt is miscible with benzene, gasoline and other kinds of chlorinated hydrocarbons, aliphatic and aromatic hydrocarbons; it is not soluble in methanol, ethanol and water, but can be dispersed in water.
PDMS Silicone Oil 350cSt is Non-flammable, non-corrosive and is chemically stable.

Product Features
PDMS Silicone Oil 350cSt having a silica structure and is liquid at room temperature and is called as siloxane, referred as silicone oils.
The simplest polydimethylsiloxane is as formula.
In, if the R, R1, R2 are all methyl groups, it is called α, ω-trimethylsilyloxy polydimethylsiloxane, that’s the commonly called silicone oil.
PDMS Silicone Oil 350cSt is a linear polymer of a low molecular weight.
If R1 and R2 are not a methyl group, then PDMS Silicone Oil 350cSt is not related to this article.
PDMS Silicone Oil 350cSt is a colorless or light yellow transparent liquid and is odorless and tasteless.
PDMS Silicone Oil 350cSt has a high boiling point and low freezing point.
The silicon-oxygen bond is very stable.

PDMS Silicone Oil 350cSt has the following features:
① low surface tension which is generally less than 209J/cm2 and is lower compared with the water and general surfactant;
② PDMS Silicone Oil 350cSt has low solubility in water and oil with high activity.
This feature allows that only a very small amount of silicone oil can already capable of reducing the surface tension of water;
③ PDMS Silicone Oil 350cSt has high stability upon heating and oxygen; This feature allows the silicone oil can be used at high temperature without being subject to decomposition;
④ PDMS Silicone Oil 350cSt has low volatility, and is chemically inert, for example, dimethicone with a viscosity of 3 × 10-2m2/s (20 ℃) ​​has a vapor pressure at 100 ℃ as low as only being 6.67 mPa while this value is 40 mPa at 220 ℃.
Moreover, it generally does not react with other substances;
⑤ PDMS Silicone Oil 350cSt has high flash point and flame retardancy;
⑥ PDMS Silicone Oil 350cSt has excellent electrical insulation ability with mold release property and anti-foaming property.

Uses
PDMS Silicone Oil 350cSt can be used as emulsifiers.
China has provided that it can be applied during the fermentation process with the maximum usage amount being 0.2g/kg.
PDMS Silicone Oil 350cSt can be used as advanced lubricants, anti-vibration oil, insulating oil, defoamers, release agents, polishes and vacuum diffusion pump oil.
PDMS Silicone Oil 350cSt can be used as the paint for prevention of moisture and rust of metal surface.
PDMS Silicone Oil 350cSt can also be used as the coating for the surfaces of buildings for prevention of water.
PDMS Silicone Oil 350cSt is used as hardening polyurethane foams additive.
PDMS Silicone Oil 350cSt can be used for applications such as: protective coatings for building materials, a cosmetic additive, a dielectric coolant, a lubricant and antiflatulent agent.
PDMS Silicone Oil 350cSt can be used for a wide range of applications such as: heat transferring medium in chemical and petrochemical industries, a dielectric coolant, protective coatings for building materials, a cosmetic additive.

Production Methods
Silicone elastomers are generally prepared from chlorosilanes.
The chlorosilanes are hydrolyzed to give hydroxyl compounds that condense to form elastomers.
Applications include electrical insulation, gaskets, surgical membranes and implants, and automobile engine components.
PE WAX (POLYETHYLENE WAX)
PE WAX (Polyethylene Wax) is a low molecular weight polyethylene polymer with the formula (C2H4)n.
PE WAX (Polyethylene Wax) has a large variety of uses and applications.


CAS NUMBER: 9002-88-4
Chemical Formula: (C2H4)n



High Density Polyethylene Wax, Polyethylene Wax, PE WAX , Polymer Wax



PE WAX (Polyethylene Wax) is a low molecular weight polyethylene polymer.
Because of it’s low molecular weight PE WAX (Polyethylene Wax) has wax like physical characteristics that include properties such as low viscosity, high hardness (brittleness) and relatively high melt point.


PE WAX (Polyethylene Wax) is a low molecular weight polyethylene polymer with the formula (C2H4)n.
PE WAX (Polyethylene Wax) has the feature of a slippery substance due to its advanced molecular structure.
PE WAX (Polyethylene Wax) is obtained from ethylene through a process called polymerization.


PE WAX (Polyethylene Wax) contains limited polyuniformity and molecular weight.
As a result, PE WAX (Polyethylene Wax) has unmatched heat stability and flexibility against other chemicals.
Polyethylene Wax, also known as PE Wax, is derived from ethylene through a process called polymerization.


Manufacturers alter the polymerization process to get a product with desired qualities.
However, certain basic properties of the material are common for all Polyethylene Wax.
PE WAX (Polyethylene Wax) is an ultra low molecular weight polyethylene consisting of ethylene monomer chains.


PE WAX (Polyethylene Wax) has a large variety of uses and applications.
PE WAX (Polyethylene Wax) is available from on-purpose production and as a byproduct of polyethylene production.
PE WAX (Polyethylene Wax) is available in both HDPE and LDPE forms.


PE WAX (Polyethylene Wax) also features limited poly disparity and molecular weight.
Consequently, PE WAX (Polyethylene Wax) is highly resistant to chemical attacks, has unmatched heat stability and is very flexible in formulating applications.


PE WAX (Polyethylene Wax) is an ultra-low molecular-weight polyethylene consisting of ethylene monomer chains.
PE WAX (Polyethylene Wax) has a large variety of uses and applications.
PE WAX (Polyethylene Wax) is available from on-purpose production and as a byproduct of polyethylene production


As a completely saturated ethylene homopolymer, PE WAX (Polyethylene Wax) is linear and crystalline.
That is why PE WAX (Polyethylene Wax) finds applications such as blends, plastic additives and rubber manufacture.
Due to its high crystalline nature, PE WAX (Polyethylene Wax) has unique features such as hardness at high temperatures and low solubility in a wide range of solvents.


PE WAX (Polyethylene Wax) is thermoplastic, so you can guess how it behaves when exposed to heat.
Thermoplastics melt of PE WAX (Polyethylene Wax) is at 110 °C.
An interesting feature of these materials is the ability to be heated and cooled without extensive degradation.


Nevertheless, you can use various methods to identify PE WAX (Polyethylene Wax) from other materials, such as sight, touch, and smell.
PE WAX (Polyethylene Wax) is similar to plastic sheets.
PE WAX (Polyethylene Wax) is a semi-translucent yellow material.


PE WAX (Polyethylene Wax) has a gloss surface.
If you cut a PE WAX (Polyethylene Wax), there are neither impurities nor any separation.
PE WAX (Polyethylene Wax) has lubricant properties, which you can feel by touch.


At room temperature, PE WAX (Polyethylene Wax) is brittle and fragile.
If you want to test the material, consider boiling PE WAX (Polyethylene Wax) in water for five minutes.
Real PE WAX (Polyethylene Wax) does not change in shape.


If PE WAX (Polyethylene Wax) contains paraffin or any other impurity, you will know it through shape change.
PE WAX (Polyethylene Wax) can be used as a disperant, slip agent, resin additive, and mold release agent.
As an oxidised product, OPEW is authorized in the EU as E number reference E914 only for the surface treatment of some fruits.


There are a variety of methods for producing PE WAX (Polyethylene Wax).
PE WAX (Polyethylene Wax) can be made by direct polymerization of ethylene under special conditions that control molecular weight and chain branching of the final polymer.


Another method involves thermal and/or mechanical decomposition of high molecular weight polyethylene resin to create lower molecular weight fractions.
A third method involves separation of the low molecular weight fraction from a production stream of high molecular weight polymer.
These last two methods produce very low molecular weight fractions that should be removed to avoid a product with low flash point that can result in flammability, migration, equipment build up, fouling and other safety and processing issues.


Volatiles in these un refined waxes can also account for significant yield loss during processing
PE WAX (Polyethylene Wax) is a low molecular weight polyethylene polymer.
Compared to natural waxes, PE WAX (Polyethylene Wax) shows a more slippery substance due to its improved molecular structure.


For this reason, PE WAX (Polyethylene Wax) is used extensively in the lubricants group.
PE WAX (Polyethylene Wax) is also used in the fields of resin additive,
mold release, hot melt adhesives, and rubber processing.


PE WAX (Polyethylene Wax) is a product used in many areas due to it’s pigment heating lubricant feature and heat resistance.
PE WAX (Polyethylene Wax)es show low solubility in solvents due to it is dense crystalline component structure.
Another purpose of use of PE WAX (Polyethylene Wax) is as a homogenizing agent in the formulation


PE WAX (Polyethylene Wax) is a low molecular weight polyethylene polymer with the formula (C2H4)n.
PE WAX (Polyethylene Wax) has the feature of a slippery substance due to its advanced molecular structure.
PE WAX (Polyethylene Wax) is obtained from ethylene through a process called polymerization.


PE WAX (Polyethylene Wax) contains limited polyuniformity and molecular weight.
As a result, PE WAX (Polyethylene Wax) has unmatched heat stability and flexibility against other chemicals.
PE WAX (Polyethylene Wax) is a prominent lubricant widely employed on exterior surfaces.


Recognized for its exceptional lubricating capabilities, PE WAX (Polyethylene Wax) aids in separating the melt from the metal, ensuring smooth interaction between metal and PVC, and enhancing a product’s shine.
These benefits are primarily due to PE WAX (Polyethylene Wax)’s innate lubricating properties.


PE WAX (Polyethylene Wax) is a low molecular weight polyethylene polymer that is utilized for its beneficial characteristics of lubrication, viscosity modulation, and improved product physical appearance.
PE WAX (Polyethylene Wax) is a semi-crystalline, hard, and brittle material, typically appearing as small pellets or flakes.


PE WAX (Polyethylene Wax) is widely recognized as a key ingredient for the lip and eye care especially sticks and mascaras.
PE WAX (Polyethylene Wax) is an excellent structurant and provides consistency to the formulation.
PE WAX (Polyethylene Wax) is an ultra low molecular weight polyethylene consisting of ethylene monomer chains.


PE WAX (Polyethylene Wax) has a large variety of uses and applications.
PE WAX (Polyethylene Wax) is available from on-purpose production and as a byproduct of polyethylene production.
PE WAX (Polyethylene Wax) is available in both HDPE and LDPE forms.


PE WAX (Polyethylene Wax) is polyethylene homopolymer wax, an excellent and consistent ingredient for end formulations to improve product physical appearance and thermal properties for a broad range of industries, including hot melt adhesives, PVC, color masterbatches, rubber and thermoplastics road markings, etc.


PE WAX (Polyethylene Wax) can be either low density polyethylene (LDPE) or high density polyethylene (HDPE).
There are three major characteristics that differentiate PE WAX (Polyethylene Wax).
Firstly, the molecular weight.


Secondly, the length of polymer branching.
And finally, the monomer or polymer composition.
Changing any of these characteristics will alter the physical characteristics of the PE WAX (Polyethylene Wax), such as viscosity, hardness, melt point and for example reactivity.


PE WAX (Polyethylene Wax) comprises a polymer chain with ethylene that has a low molecular weight.
Mainly, PE WAX (Polyethylene Wax) exists as a by-product of the polymerization of crude oil into ethylene.
PE WAX (Polyethylene Wax) is classified into HDPE wax and LDPE wax.


Typically, HDPE is more crystalline and denser, so if you have a way of determining these properties, you can distinguish the difference between these variations.
Due to its PE WAX (Polyethylene Wax)’s low molecular weight and poly disparity, it has outstanding heat stability, is flexible, and is highly resistant to chemicals.


PE WAX (Polyethylene Wax) is a type of synthetic wax derived from the polymerization of ethylene gas.
PE WAX (Polyethylene Wax) is commonly produced through the high-pressure polymerization of ethylene using specialize catalysts.
PE WAX (Polyethylene Wax) is derived from ethylene through a process called polymerization.


Manufacturers alter the polymerization process to get a product with desired qualities.
However, certain basic properties of the material are common for all PE WAX (Polyethylene Wax).
As a completely saturated ethylene homopolymer, PE WAX (Polyethylene Wax) is linear and crystalline.


That is why PE WAX (Polyethylene Wax) finds applications such as blends, plastic additives and rubber manufacture.
Due to its high crystalline nature, PE WAX (Polyethylene Wax) has unique features such as hardness at high temperatures and low solubility in a wide range of solvents.


PE WAX (Polyethylene Wax) can be either low-density polyethylene (LDPE) or high-density polyethylene (HDPE).
Generally, HDPE tends to be more dense and crystalline, so you could distinguish the two if you have a way of determining these properties.
Nevertheless, you can use various methods to identify PE WAX (Polyethylene Wax) from other materials, such as sight, touch, and smell.


PE WAX (Polyethylene Wax) is similar to plastic sheets.
PE WAX (Polyethylene Wax) is a semi-translucent yellow material.
PE WAX (Polyethylene Wax) has a gloss surface.


If you cut a PE WAX (Polyethylene Wax), there are neither impurities nor any separation.
PE WAX (Polyethylene Wax) has lubricant properties, which you can feel by touch.
At room temperature, PE WAX (Polyethylene Wax) is brittle and fragile.


This is unlike a fake version, which is rough and greasy.
If you want to test PE WAX (Polyethylene Wax)l, consider boiling it in water for five minutes.
Real PE WAX (Polyethylene Wax) does not change in shape.
If PE WAX (Polyethylene Wax) contains paraffin or any other impurity, you will know it through shape change.



USES and APPLICATIONS of PE WAX (POLYETHYLENE WAX):
The resulting PE WAX (Polyethylene Wax) has a wide range of applications due to its unique properties.
PE WAX (Polyethylene Wax) is used in different applications across the world.
PE WAX (Polyethylene Wax) works as a critical raw material in the production of coatings, cosmetics, PVC products, and inks.


PE WAX (Polyethylene Wax) is used as a dispersant in the production of color masterbatch.
PE WAX (Polyethylene Wax) increases the wax product’s strength and softening point for a good gloss.
PE WAX (Polyethylene Wax) helps ensure that candles burn brightly and safely without producing a cloud of black smoke.


In the PVC industry, PE WAX (Polyethylene Wax) is used in the molding process as an internal lubricant.
This helps enhance the toughness of pipe and other plastic products.
PE WAX (Polyethylene Wax) ensures that the PVC products have an improved pass rate and are smooth.


In the production of PVC film, PE WAX (Polyethylene Wax) can enhance the film’s transparency and gloss and improve its transverse and longitudinal toughness.
In ink and coatings industries, PE WAX (Polyethylene Wax) is used as a dispersant since it provides a tremendous anti-selling effect.


PE WAX (Polyethylene Wax) helps ensure that the printed matter has a three-dimensional effect and good gloss.
Adding as little as 1% of PE WAX (Polyethylene Wax) to the ink can affect its fluidity and reduce its viscosity.
Besides, PE WAX (Polyethylene Wax) improves abrasion and scratch resistance and enhances the smoothness of the ink.


PE WAX (Polyethylene Wax) speeds up color fixing, increases hydrophilicity, and completes printing dots.
At the same time, PE WAX (Polyethylene Wax) can reduce the effects of plucking and caking and enhance the printing capabilities of the ink.
PE WAX (Polyethylene Wax) can be emulsified in water and dispersed in organic solvents to make wax emulsion or dispersion of appropriate particle size.


PE WAX (Polyethylene Wax) is used Coatings and inks.
PE WAX (Polyethylene Wax) is used slip and anti-blocking agent.
PE WAX (Polyethylene Wax) is often employ as a slip agent in coatings and inks to reduce the coefficient of friction between surfaces.


PE WAX (Polyethylene Wax) helps in improving the smoothness and slipperiness of the coating or ink film, preventing sticking or blocking when surfaces come into contact.
This property is particularly useful in applications of PE WAX (Polyethylene Wax) such as paper coatings, flexible packaging, and graphic arts.


Consequently, PE WAX (Polyethylene Wax) is highly resistant to chemical attacks and has a good heat stability.
Extrusion processing is used as lubrication and injection process.
PE WAX (Polyethylene Wax) is used as a lubricant for HDPE, PP AND PVC.


PVC composite is used as a stabilizer.
PE WAX (Polyethylene Wax) is used as a lubricant and dispersion in compound production.
PE WAX (Polyethylene Wax) also contributes to easy processing by allowing the material to separate from the mold while being processed.


PE WAX (Polyethylene Wax) is used as a lubricant in cable installation.
PE WAX (Polyethylene Wax) is used to improve abrasibility in paint, to increase durability, and as a pigment developer and decomposable carrier.
PE WAX (Polyethylene Wax) is used in floor polishers with high polymer content.


PE WAX (Polyethylene Wax) is used to provide opacity in candle production.
PE WAX (Polyethylene Wax) is used at a rate of 5-10% to ensure dispersion of the filling material.
PE WAX (Polyethylene Wax) is used to increase the strength of car polish.


PE WAX (Polyethylene Wax) is used as a dispersant in thermosetting paints (road marking paint) to add shine and three dimensions.
PE WAX (Polyethylene Wax) is used as a film-forming auxiliary to increase the resistance of paper against scratching and mechanical movements.
PE WAX (Polyethylene Wax) is used in the cosmetics industry to provide shine in make-up products.


PE WAX (Polyethylene Wax) is used as a softener and lubricant to increase the durability of fibers and to prevent tearing.
PE WAX (Polyethylene Wax) is used in polyurethane coatings to provide resistance against abrasion.
PE WAX (Polyethylene Wax) is used in water-based printing inks and overprint varnishes to increase wear resistance and reduce sliding friction.


PE WAX (Polyethylene Wax) market to include plastic additives, candles, cosmetics and rubber.
Other uses of PE WAX (Polyethylene Wax) are packaging, lubricants, wood, and coatings.
PE WAX (Polyethylene Wax) is used in the Production of plastic and injection molding industries.


PE WAX (Polyethylene Wax) is used in the Production of water and wastewater pipes and gas pressure pipes.
PE WAX (Polyethylene Wax) is used in the production of PVC pipes.
PE WAX (Polyethylene Wax) is used in the production of Cables wires.


PE WAX (Polyethylene Wax) is used refined PE waxes are non-toxic and are used in food too, cosmetics, and healthy products.
PE WAX (Polyethylene Wax) is used in rubber industries as a lubricant.
In the Production of all kinds of candles, PE wax will increase the thermal resistance and hardness of candles.


PE WAX (Polyethylene Wax) is used in order to prevent oxidizing the metal surface during the coating process.
PE WAX (Polyethylene Wax) is used in the production of Master batch (Masterbatch) for better distribution of pigments and controlling the pressure in the process of production master batch.


PE WAX (Polyethylene Wax) is used in asphalt as an additive.
PE WAX (Polyethylene Wax) is used in the ink and color toner industry.
In Hot melt adhesive, PE WAX (Polyethylene Wax) by increasing the temperature of congelation without increasing viscosity will cause enhance (improve) the function of hot melt adhesive at high temperatures.


PE WAX (Polyethylene Wax) is used in emulsions.
PE WAX (Polyethylene Wax) would be a widely used type of polyethylene in the world.
PE WAX (Polyethylene Wax) according to their applications will have two types:


PE WAX (Polyethylene Wax) is used as a processing aid (PA) and lubricant (Used to achieve the quality and improvement of the production process of PVC & Polymer)
PE WAX (Polyethylene Wax) is used as a basic material or additive will participate in improving and modifying the properties of the final product.


PE WAX (Polyethylene Wax) using decrease the friction so increase the extrusion capacity.
PE WAX (Polyethylene Wax) using doesn’t change the product color because PE wax has got good oxidation resistance.
PE WAX (Polyethylene Wax) doesn’t bad effect product’s heat and light stability because pe wax doesn’t include catalizors remnant.


PE WAX (Polyethylene Wax) increase last product’s light stability.
PE WAX (Polyethylene Wax) hasn’t got toxic materials so PE wax can be use food packaging applications.
PE WAX (Polyethylene Wax) is used hot melt application.


PE WAX (Polyethylene Wax) have very unique polymer properties that make them useful in many applications.
The major functions of PE WAX (Polyethylene Wax) in many formulations are to either provide lubrication and/or provide physical modification of a formula by changing viscosity and / or melt point.


PE WAX (Polyethylene Wax) is used hot melt (increasing the solidification point of adhesives without increasing the viscosity of the mixture, improving the behaviour of hot melts at high temperatures).
PE WAX (Polyethylene Wax) is used to disperse loads and pigments (masterbatch).


PE WAX (Polyethylene Wax) is used coating paper (improving gloss and flexibility, achieving high-quality finishes).
PE WAX (Polyethylene Wax) process aids to make mixtures of rubber and PVC, among others, more processable.
PE WAX (Polyethylene Wax) is used manufacturing inks and toners, Additives in paraffin mixtures, Products for filling cables, Additives for asphalt, Emulsions, Textile, Polishes, and Candles (providing increased hardness and thermal resistance).


PE WAX (Polyethylene Wax) has very unique polymer properties that make them useful in many applications.
The major functions of PE WAX (Polyethylene Wax) in many formulations are to either provide lubrication and/or provide physical modification of a formula by changing viscosity and / or melt point.


PE WAX (Polyethylene Wax) increases inorganic and organic pigment dispersion in matrix polymer during masterbach processing.
Also, PE WAX (Polyethylene Wax) helps granule produce by decrease softening point of system.
PE WAX (Polyethylene Wax) is very good external lubricant for PVC.


When PE WAX (Polyethylene Wax) use in PVC application, final produce face has been shine.
PE WAX (Polyethylene Wax) is used plastic additives, candles, cosmetics and rubber.
PE WAX (Polyethylene Wax) is used packaging, lubricants, wood and coatings.


PE WAX (Polyethylene Wax) finds application in a wide range of industries because of its desirable physical and chemical properties.
As PE WAX (Polyethylene Wax) can have a broad range of melt points, densities and other properties, it is understandable why it is used so extensively.
The emulsifiable variety is particularly crucial in the textile industry.


PE WAX (Polyethylene Wax) is also used in paper coating, leather auxiliaries, crayons and cosmetics.
The non-emulsifiable type is most common in printing ink, pigment concentrates and paints.
In the textile sector, PE WAX (Polyethylene Wax) probably finds the most intensive application.


Emulsions made from PE WAX (Polyethylene Wax) offer stable softening.
While they resist acids and other chemicals, these emulsions are friendly to the fabric – with no yellowing of fabrics, no colour change and no chlorine retention.


The packaging sector is also using PE WAX (Polyethylene Wax) intensively.
PE WAX (Polyethylene Wax) has very unique polymer properties that make them useful in many applications.
The major functions of PE WAX (Polyethylene Wax) in many formulations are to either provide lubrication and/or provide physical modification of a formula by changing viscosity and / or melt point.


-The coating industry has historically used waxes.
The importance of PE WAX (Polyethylene Wax) is that it adds water-repellency, better slip, and mark resistance among other features.
When used correctly, PE WAX (Polyethylene Wax) introduces the following:
*Anti-sagging
*Anti-settling
*Abrasion resistance
*Marking resistance
*Mar resistance

In the inks industry, PE WAX (Polyethylene Wax) presents similar advantages.
Most ink types contain PE WAX (Polyethylene Wax) as a way to improve the coefficient of friction and increase scuff.



7 USES OF PE WAX (POLYETHYLENE WAX):
PE WAX (Polyethylene Wax) is available in powder form, milky white small glass microbead form and block form.
PE WAX (Polyethylene Wax) has low viscosity, high softening point, good strength and other properties, non-toxic, good heat resistance, low high temperature volatiles, dispersion of color paste, not only has excellent external lubricity, but also has strong internal lubrication effect.

PE WAX (Polyethylene Wax) can improve the productivity of plastic granulation, good moisture resistance at room temperature, strong chemical resistance, good electrical properties.
PE WAX (Polyethylene Wax) can improve the appearance of finished products.

Because of its excellent external lubrication and strong internal lubrication, PE WAX (Polyethylene Wax) is compatible with high-pressure polyethylene, polyethylene, polypropylene and other epoxy resins.
PE WAX (Polyethylene Wax) can be used as a lubricant in extrusion, injection molding and injection production processing.

PE WAX (Polyethylene Wax) can improve production and processing efficiency, avoid and get rid of plastic film, pipe fittings, plastic sheet bonding, improve the smoothness and smoothness of finished products, and improve the appearance of finished products.

PE WAX (Polyethylene Wax) can be used as a dispersant for a wide variety of thermoplastic masterbatches and a lubricant dispersant for plastic filling masterbatches and dissolving masterbatches, and can improve the production and processing performance, surface gloss, lubricity and heat resistance of HDPE, PP and PVC.

PE WAX (Polyethylene Wax) is used as internal dispersant in masterbatch production and processing, it is commonly used in high-pressure polyethylene hydrocarbon plastic masterbatch.
PE WAX (Polyethylene Wax) is used as color paste dispersant, lubricant and polishing liquid in the production process of PVC profile, pipe, tube, PE and PP molding.

PE WAX (Polyethylene Wax) lubricant improve the melting level, the ductility and surface gloss of plastic products.
PE WAX (Polyethylene Wax) can be used as dispersant and polishing liquid for printing ink and lacquer, especially for road marking paint and line painting paint, which has excellent anti-settlement effect and makes the products have good gloss and hierarchy.

PE WAX (Polyethylene Wax) is used in the production of various hot solvents, thermosetting plastic electrostatic powder, and PVC compound thickener.
PE WAX (Polyethylene Wax) is commonly used in the production of automobile wax, car wax, varnish wax, and wax products of various kinds of wax products, to improve the softening point of wax products, to enhance their compressive strength and surface smoothness.

In the field of vulcanized rubber, PE WAX (Polyethylene Wax) improves the surface gloss and luster of the product after de-filming, reduces the amount of paraffin used, and reduces the cost of the product.

PE WAX (Polyethylene Wax) is used in oil-based printing ink and architectural coatings, generally choose air oxidized polyethylene wax, add emulsion breakers to make moisturizing emulsion or dispersion and acrylic emulsion.
Air oxidized PE WAX (Polyethylene Wax) improves its water absorption in a sense.



IN WHICH AREAS IS PE WAX (POLYETHYLENE WAX) USED ?
*Cable Industry
*Paint Industry
*Furniture Industry
*Window Profile Industry
*Plastic Industry
*Leather Industry
*Masterbatch production



FEATURES OF PE WAX (POLYETHYLENE WAX):
1. High softening point, low viscosity, large molecular weight and small heat loss.
2. PE WAX (Polyethylene Wax) has strong external lubricating effect.
Compared with ordinary PE WAX (Polyethylene Wax), it can delay plasticization and reduce torque.
3. PE WAX (Polyethylene Wax) is easy to disperse and improve the glossiness of products.
4. Good compatibility and anti-precipitation.
5. Good mold release, good metal peeling, long continuous production time.
6. Good thermal stability in the later stage, free of oligomers, paraffin, etc.



PROPERTIES OF PE WAX (POLYETHYLENE WAX):
properties of PE WAX (Polyethylene Wax) is characterized by its low molecular weight and linear structure.
PE WAX (Polyethylene Wax) typically exists as a solid, white or light yellow-color material with a waxy texture. Some key properties of wax include:

*Low melting point:
Low melting PE WAX (Polyethylene Wax) has a relatively low melting point, which allows it to melt easily and provide lubrication at low temperatures.

*High hardness:
PE WAX (Polyethylene Wax) possesses a high degree of hardness, making it useful for applications that require abrasion resistance and durability.

*Low viscosity:
Low viscosity PE WAX (Polyethylene Wax) has a low viscosity, meaning it flows easily and provides excellent internal lubrication.

*Chemical resistance:
PE WAX (Polyethylene Wax) exhibits good resistance to many chemicals, including acids, alkalis, and organic solvents.



FEATURES OF PE WAX (POLYETHYLENE WAX):
*High melting point
*High chemical resistance
*Outstanding thermal stability
*Perfect lubricant
*High softening point
*High head resistance
*Compatible with other wax varieties



PE WAX (POLYETHYLENE WAX) IS AVAILABLE IN VARIOUS FORMS, INCLUDING:
*Flakes
*Granules
*Lumps
*Powder



CHARACTERISTICS & FEATURES OF PE WAX (POLYETHYLENE WAX):
*High softening point
*High melting point
*Excellent thermal stability
*High chemical resistance
*Highly compatible with wax varieties
*Perfect lubrication
*Perfect head resistance



FUNCTIONS OF PE WAX (POLYETHYLENE WAX):
*High binding strength
*Gelling agent
*Viscosity modifier
*Plasticizer
*Improves structure, oil retention, and pay-off for stick applications



COMPATIBILITY OF PE WAX (POLYETHYLENE WAX):
Polyethylene Wax is compatible with many vegetable and mineral waxes and a variety of natural and synthetic ingredients.



PRODUCTION PROCESS OF PE WAX (POLYETHYLENE WAX):
The production of Polyethylene Wax (PE Wax) is closely tied to the polymerization and subsequent processing of polyethylene.
Several methods are commonly used to produce PE Wax, and the choice of process often depends on the required properties of the end product.
Here’s an overview of some common production processes:

1. Polymerization:
*Ethylene Gas:
The primary raw material, ethylene gas, is polymerized to create polyethylene.

*Catalysts:
Ziegler-Natta catalysts or metallocene catalysts are often used to initiate the polymerization.


2. Cracking:
*High Molecular Weight Polyethylene:
To convert high molecular weight polyethylene to PE Wax, a thermal or catalytic cracking process is employed.

*Outcome:
This reduces the molecular weight and produces PE Wax along with other polyethylene by-products.


3. Oxidation:
Air or Oxygen: Introduced to polyethylene at elevated temperatures.
*Purpose:
To create oxidized PE Waxes that have functional groups, improving compatibility with polar resins.


4. Solvent Recovery:
In some methods, solvents are used to purify or modify the PE Wax.

*Distillation:
Solvents are typically recovered by distillation and can be reused in the process.


5. Additives:
*Modifiers:
Functional groups, stabilizers, or lubricants are added to enhance specific properties.

*Mixing:
Thorough mixing ensures even distribution of additives.


6. Extrusion or Pelletizing:
*Form:
The final PE Wax is often formed into pellets or flakes for easier handling and application.

*Cutting:
Specialized equipment is used to cut or form the wax into the desired shape and size.


7. Quality Control:
Testing:
The PE Wax undergoes a series of tests to confirm it meets specified quality standards.



CHARACTERISTICS OF PE WAX (POLYETHYLENE WAX):
*High softening point
*High melting point
*Excellent thermal stability
*High chemical resistance
*Highly compatible with wax varieties
*Perfect lubrication
*Perfect head resistance



PROPERTIES AND FEATURES OF PE WAX (POLYETHYLENE WAX):
PE WAX (Polyethylene Wax) is derived from ethylene through a process called polymerization.
Manufacturers alter the polymerization process to get PE WAX (Polyethylene Wax) with desired qualities.
However, certain basic properties of the material are common for all PE WAX (Polyethylene Wax).

As a completely saturated ethylene homopolymer, PE WAX (Polyethylene Wax) is linear and crystalline.
That is why PE WAX (Polyethylene Wax) finds applications such as blends, plastic additives and rubber manufacture.
Due to its high crystalline nature, PE WAX (Polyethylene Wax) has unique features such as hardness at high temperatures and low solubility in a wide range of solvents.

PE WAX (Polyethylene Wax) is thermoplastic, so you can guess how it behaves when exposed to heat.
Thermoplastics melt of PE WAX (Polyethylene Wax) at 110 °C.
An interesting feature of these materials is the ability to be heated and cooled without extensive degradation.

PE WAX (Polyethylene Wax) also features limited poly disparity and molecular weight.
Consequently, PE WAX (Polyethylene Wax) is highly resistant to chemical attacks, has unmatched heat stability and is very flexible in formulating applications.



FEATURES OF PE WAX (POLYETHYLENE WAX):
Polyethylene Wax Technical Details
Ultra-low molecular weight polyethylene (average number of molecular weight Min less than 10,000) has the properties and functions like Wax.
PE WAX (Polyethylene Wax) would be produced through polymerization in high pressure with catalysts that contain Oxygen or polymerization in low pressure by using Ziegler, Natta catalyst or breaking chains way.

Most of the manufacturers of PE WAX (Polyethylene Wax) refined the end materials of different grades of High-Density Polyethylene such as BL3, EX3, EX5, and 0035 by removing Hexane, Alcohol, and volatiles (moisture and oil) to make a high-quality and crispy PE WAX.
All PE WAX (Polyethylene Wax) grades have the same structures but the final products would have different features because of different processes of production.

PE WAX (Polyethylene Wax) is widely used in the purpose to reduce viscosity in different industries.
Functional PE WAX (Polyethylene Wax) has both physical and Chemical properties of PE WAX (Polyethylene Wax) and oxygenated materials.
PE WAX (Polyethylene Wax) has uses in different industries as dispersants of pigments, additives for inks, plastics productions, cosmetics productions, colors toner, and Adhesives industries.

PE WAX (Polyethylene Wax) is a by-product material from BL3, EX5, f7000, 0035, and X3 of petrochemical that is made from first-class polyethylene lump.
PE WAX (Polyethylene Wax) has less strength and flexibility in comparison to other polyethylene, but its resistance in front of chemicals and external pressures is very high.

The PE WAX (Polyethylene Wax) quality would be under the effects of viscosity, melting point, density, and the ability to migrate to the surface and its color.
PE WAX (Polyethylene Wax) flake color of PETRO-ACC would be completely white (not yellowish) and without black dots on it with below 3% of volatile materials.

PE WAX (Polyethylene Wax) has a good function as a lubricant, via Ball Bearing Mechanism you can check and examine its lubricant property.
In this mechanism PE WAX (Polyethylene Wax) particles migrate to the surface and as an interface will cover the surface and will prevent the material surface from contacting with the surface of the machines and molds.



WHAT IS THE DIFFERENCE BETWEEN FULLY REFINED AND RAW PE WAX (POLYETHYLENE WAX)?
Raw PE WAX (Polyethylene Wax) is derived from extracting low molecular weight fractions from high density polyethylene resin streams.
These streams contain contaminants and non – wax fractions such as catalyst, volatile fractions and water.
Refined PE WAX (Polyethylene Wax) derived from high density polyethylene resin manufacturing processes undergo an extensive refining process that removes catalyst, volatile fractions and water.
The final product is usually finished by prilling into 1 to 3 mm free flowing prills.



DURABILITY OF PE WAX (POLYETHYLENE WAX):
Durability is a key factor when evaluating the quality and applicability of PE WAX (Polyethylene Wax) in various industrial sectors.
Here’s what you need to know about the durability of PE WAX (Polyethylene Wax):

1. Thermal Stability:
PE WAX (Polyethylene Wax) generally exhibits good thermal stability, which is essential for high-temperature applications like hot-melt adhesives and plastic processing.

2. Chemical Resistance:
PE WAX (Polyethylene Wax) is chemically inert in most conditions, making it resistant to various solvents, acids, and bases.
However, oxidized grades may react differently.

3. Long Shelf Life:
When stored under proper conditions, PE WAX (Polyethylene Wax) can have an extended shelf life, often ranging from 2 to 5 years depending on the manufacturer’s guidelines.

4. Mechanical Durability:
PE WAX (Polyethylene Wax) can enhance the mechanical properties of composite materials, providing added durability to the finished product.

5. UV Resistance:
Some grades of PE WAX (Polyethylene Wax) can offer UV stability, thereby increasing the lifespan of products exposed to sunlight.

6. Oxidation:
While generally stable, PE WAX (Polyethylene Wax) can be oxidized to create oxidized waxes with different characteristics.
Oxidation, if unintended, could affect the product’s durability.

7. Moisture Resistance:
PE WAX (Polyethylene Wax) is hydrophobic, making it resistant to water absorption, which in turn contributes to its durability.

8. Compatibility:
PE WAX (Polyethylene Wax)'s compatibility with other polymers and additives can influence the overall durability of the end product in composite materials or blends.

9. Wear and Tear:
In lubrication applications, PE WAX (Polyethylene Wax) can reduce wear and tear, extending the life of mechanical parts.
For specific applications, it’s crucial to consult the technical data sheets and conduct necessary tests to ensure the PE WAX (Polyethylene Wax) grade you’re considering meets your durability requirements.
Always align the choice of PE WAX (Polyethylene Wax) with its intended application for optimal durability.



PERFORMANCE OF PE WAX (POLYETHYLENE WAX):
Performance attributes of PE WAX (Polyethylene Wax) determine its efficacy in a wide range of applications.
These attributes are influenced by its molecular weight, level of refinement, type (e.g., oxidized or non-oxidized), and any additives present.
Below are key performance characteristics:

1. Lubricity:
PE WAX (Polyethylene Wax) serves as an excellent internal and external lubricant for PVC and other plastics, facilitating smooth processing and enhancing surface properties.

2. Viscosity Control:
In liquid formulations, like inks and coatings, PE WAX (Polyethylene Wax) plays a role in controlling and reducing viscosity.

3. Dispersibility:
PE WAX (Polyethylene Wax) enhances the dispersion of pigments and fillers in color masterbatches and printing inks.

4. Gloss and Surface Finish:
PE WAX (Polyethylene Wax) can enhance the gloss and smoothness of surfaces in applications like paints, varnishes, and coatings.

5. Adhesion:
While PE WAX (Polyethylene Wax) itself isn’t inherently adhesive, its presence can modify the adhesion properties of certain formulations, like hot melt adhesives.

6. Heat Stability:
PE WAX (Polyethylene Wax) shows stability under elevated temperatures, crucial for plastic processing, extrusion, and molding applications.

7. Scratch Resistance:
When used in coatings or surface treatments, PE WAX (Polyethylene Wax) provides improved resistance to scratching and marring.

8. Water Repellency:
PE WAX (Polyethylene Wax)'s hydrophobic nature imparts water-repellent properties to treated surfaces or materials.

9. Chemical Inertness:
PE WAX (Polyethylene Wax) is chemically stable and doesn’t react with most substances, which is advantageous in ensuring the integrity of formulations.

10. Compatibility:
PE WAX (Polyethylene Wax)’s compatible with various polymers and resins, which makes it a versatile additive in a wide array of applications.

11. Blocking Resistance:
PE WAX (Polyethylene Wax) can be used to reduce or eliminate the blocking tendency (unwanted adhesion between layers) in films or sheets.

12. Melt Point:
The melting point can vary based on the grade and is an important factor in determining PE WAX (Polyethylene Wax)'s suitability for specific applications.
When selecting a PE WAX (Polyethylene Wax) for a specific application, understanding these performance attributes is vital.



COMPONENTS AND MATERIALS OF PE WAX (POLYETHYLENE WAX):
PE WAX (Polyethylene Wax) is a synthesized wax primarily derived from polyethylene, a polymer made from ethylene monomers.
While the basic constitution of PE WAX (Polyethylene Wax) is polyethylene, its overall composition and properties can vary based on the processing method and any additives or modifiers used.
Here’s a breakdown of PE WAX (Polyethylene Wax)'s components and related materials:

1. Base Component:
Polyethylene:
As the name suggests, PE WAX (Polyethylene Wax) is primarily composed of polyethylene. It’s a type of thermoplastic polymer made from ethylene monomers.
PE WAX (Polyethylene Wax) is essentially a lower molecular weight version of polyethylene.


2. Modifiers (for specific grades or types):
Functional Groups:
For some PE WAX (Polyethylene Wax), especially oxidized variants, functional groups like carboxylic acids or alcohols might be introduced to enhance certain properties.

*Stabilizers:
To enhance the thermal stability of PE WAX (Polyethylene Wax), especially when used in high-temperature applications.

*Plasticizers:
Occasionally added to modify the flexibility or moldability of PE WAX (Polyethylene Wax).


3. Additives (to cater to specific applications):
*Lubricants:
Sometimes added to enhance the lubricating properties of PE WAX (Polyethylene Wax) in certain applications.

*Dyes or Pigments:
When color is required, especially in cosmetic or decorative applications.

*Fillers:
Materials like talc or calcium carbonate might be added to alter the physical properties of the wax.


4. Residual Catalysts:
Traces of catalysts, like Ziegler-Natta catalysts, might be present if they were used in the polymerization of ethylene.


5. Impurities:
Depending on the refining and purification process, minute amounts of other petrochemical derivatives or residual solvents might be present.
When sourcing PE WAX (Polyethylene Wax) or using it for specific applications, it’s essential to check its specification sheet or material data sheet.



HOW IS PE WAX (POLYETHYLENE WAX) MADE?
There are a variety of methods for producing PE WAX (Polyethylene Wax).
PE WAX (Polyethylene Wax) can be made by direct polymerization of ethylene under special conditions that control molecular weight.
Another method involves breaking down high molecular weight polyethylene into lower molecular weight fractions.
A third method involves separation of the low molecular weight fraction from high molecular weight polymer.



DIFFERENCES BETWEEN PE WAXES (POLYETHYLENE WAX) TYPE:
There are three major characteristics that differentiate one PE wax from another.
They are
I) Molecular weight,
II) Degree and length of polymer branching,
III) Monomer / polymer composition.
Changing any of these factors will alter the physical characteristics of the PE WAX (Polyethylene Wax), such as viscosity, hardness, melt point, reactivity etc.



DIFFERENCES BETWEEN PE WAX (POLYETHYLENE WAX) AND PARAFFIN WAX:
Paraffin wax is usually produced as a by-product of oil refining.
It has a molecular weight which is usually less than half that of most PE WAX (Polyethylene Wax).
Because of this and other differences, paraffin wax usually has a much lower melt point and is softer than most PE WAX (Polyethylene Wax).



SPECIFICATION OF PE WAX (POLYETHYLENE WAX):
PE WAX (Polyethylene Wax) is heat-stable, lowly soluble, chemically resistant and hard.
Combining these features with abrasion resistance and broad melting points makes PE WAX (Polyethylene Wax) the undisputable choice for a wide range of industrial applications.



THE DIFFERENCE BETWEEN PE WAX (POLYETHYLENE WAX) AND POLYETHYLENE:
PE WAX (Polyethylene Wax) is a chemical material that behaves in the form of small white microbeads or flakes, with a high melting point, high hardness, high gloss, snow-white color, etc.
PE WAX (Polyethylene Wax) is often used in coatings, inks, dermis, cosmetics, etc. and plays an important role.

Polyethylene is the raw material of PE, which is a polymer made by polymerization of ethylene monomer.
Polyethylene is divided into high-density polyethylene, low-density polyethylene and linear low-density polyethylene depending on the polymerization method, molecular weight and chain structure.

Low density polyethylene, commonly known as high pressure polyethylene, is mainly used in plastic bags, agricultural films, etc. because of its low density and softest material.

High density polyethylene, commonly known as low pressure polyethylene, has higher temperature resistance, oil resistance, steam penetration resistance and environmental stress cracking resistance compared to LDPE and LLDPE, in addition to good electrical insulation and impact resistance and cold resistance, and is mainly used in blow molding and injection molding.

LLDPE is similar to LDPE in appearance, less transparent, but with good surface gloss, low temperature toughness, high modulus, bending resistance and stress cracking resistance, and better impact strength at low temperature.

PE WAX (Polyethylene Wax) is an additive in the production, has good dispersibility and lubricity.
These are the difference between PE WAX (Polyethylene Wax) vs polyethylene.



PE WAX (POLYETHYLENE WAX); HS CODE, CHEMICAL FORMULA, AND CAS NUMBER
To facilitate international trade, standardize product categorization, and ensure proper tracking, various codes and identifiers are used.
Here are the fundamental details for PE WAX (Polyethylene Wax):

HS Code:
The Harmonized System (HS) Code for PE WAX (Polyethylene Wax) can vary based on the region and specific grade of the product.
A commonly used HS code for PE WAX (Polyethylene Wax) is 3404.90, but it’s essential to check with local customs and trade regulations for the most accurate and current code for your region.

Chemical Formula:
PE WAX (Polyethylene Wax) is a polymer, so it doesn’t have a fixed chemical formula like small molecules.
However, PE WAX (Polyethylene Wax)'s base unit, which repeats in the polymer chain, is derived from ethylene with the formula -CH2-CH2-.

CAS Number:
The Chemical Abstracts Service (CAS) number for Polyethylene is 9002-88-4.
It’s worth noting that CAS numbers are assigned to every chemical described in open scientific literature, ensuring a unique identifier.

For specific trade or manufacturing operations, it’s recommended to verify these details with relevant industry bodies, regulatory agencies, or trusted suppliers to ensure accuracy and compliance.



ORIGIN OF PE WAX (POLYETHYLENE WAX):
PE WAX (Polyethylene Wax) can be derived through various processes, including the direct polymerization of ethylene, degradation of high molecular weight polyethylene resin, or direct synthesis from lower molecular weight ethylene homopolymers.



PHYSICAL APPEARANCE OF PE WAX (POLYETHYLENE WAX):
Usually seen in the form of white beads, flakes, or powders.
PE WAX (Polyethylene Wax) might also be available in a prill form.



PROPERTIES OF PE WAX (POLYETHYLENE WAX):
PE WAX (Polyethylene Wax)’s known for its excellent resistance to chemical agents, thermal stability, and a high melting point.
Due to its nature, PE WAX (Polyethylene Wax) offers reduced internal and external friction.



COMPATIBILITY OF PE WAX (POLYETHYLENE WAX):
PE WAX (Polyethylene Wax) exhibits compatibility with a plethora of materials, which makes it versatile in its applications.
PE WAX (Polyethylene Wax)’s often mixed with paraffin waxes to enhance certain characteristics.



UTILITY OF PE WAX (POLYETHYLENE WAX):
Predominantly PE WAX (Polyethylene Wax) is used as a lubricant, flow improver, or processing aid, particularly in the plastics industry.
Moreover, PE WAX (Polyethylene Wax) serves as a dispersing agent for pigments and fillers.

Remember, while PE WAX (Polyethylene Wax) is prevalent in numerous industries, it’s crucial to select the appropriate grade and type to suit specific applications, ensuring optimal performance.



PE WAX (POLYETHYLENE WAX) TYPES AND GRADES:
Understanding the types and grades of PE WAX (Polyethylene Wax) is essential for choosing the right variant for your specific application. Here are the primary categories:

Types:
*Low-Density PE WAX (Polyethylene Wax):
Lighter in weight, used in applications that require less rigidity and more flexibility.

*High-Density PE WAX (Polyethylene Wax):
Offers more rigidity and is suited for more demanding applications, including industrial-grade lubricants.

*Oxidized PE WAX (Polyethylene Wax):
Treated to include oxygen-containing functional groups, this type is often used as an emulsifier.

*Non-Oxidized PE WAX (Polyethylene Wax):
Generally used as a lubricant and friction reducer.

*Functionalized PE WAX (Polyethylene Wax):
Modified for special purposes, such as to improve adhesion or compatibility with polar resins.

*Grades:
Industrial Grade:
PE WAX (Polyethylene Wax) is ideal for use in heavy-duty applications like road construction, industrial lubricants, and paint manufacturing.

*Food-Grade:
PE WAX (Polyethylene Wax) meets strict safety guidelines and is suitable for food packaging materials.

*Pharmaceutical Grade:
PE WAX (Polyethylene Wax) passes rigorous purity tests and is used in pharmaceutical applications.

*Cosmetic Grade:
PE WAX (Polyethylene Wax) is utilized in the manufacture of cosmetics and personal care products, adhering to stringent safety and quality standards.

*Custom Grades:
Sometimes, PE WAX (Polyethylene Wax) is custom-formulated to meet specific requirements, including varying molecular weights or containing specialized additives for particular applications.

When selecting a PE WAX (Polyethylene Wax), it’s crucial to consult with suppliers and experts to understand which type and grade will best meet your needs.
Always consider factors such as thermal stability, hardness, and chemical resistance when making your selection.



SOME CHARACTERISTICS OF PE WAX (POLYETHYLENE WAX):
*High softening point
*High melting point
*Excellent thermal stability
*High chemical resistance
*Highly compatible with wax varieties
*Perfect lubrication
*Perfect head resistance



HOW DOES PE WAX (POLYETHYLENE WAX) DIFFER FROM PARAFFIN AND OTHER WAXES?
Paraffin wax is usually produced as a by-product of oil refining.
It has a molecular weight which is usually less than half that of most PE WAX (Polyethylene Wax).

Because of this and other differences, paraffin wax usually has a much lower melt point and is softer than most PE WAX (Polyethylene Wax).
FT waxes are another class of waxes that are only produced by a limited number of suppliers (i.e. Shell and Sasol) due to the large capital requirements involved in constructing these plants.

FT waxes are produced in the process of making synfuels.
Variations in properties of FT waxes are generally limited to modifying melt point.



HISTORY OF PE WAX (POLYETHYLENE WAX):
The story of PE WAX (Polyethylene Wax), much like other petrochemical derivatives, is deeply rooted in the evolution of polymer science and the oil and gas industry.
Here’s a brief chronology of its development:

1930s:
Polyethylene, the base material for PE WAX (Polyethylene Wax), was discovered by scientists Eric Fawcett and Reginald Gibson at the ICI (Imperial Chemical Industries) company in England.
They produced polyethylene accidentally while attempting to react ethylene under high pressure with benzaldehyde.

Late 1930s to 1940s:
The potential of Polyethylene as a revolutionary plastic was recognized.
With World War II looming, the material’s insulation properties made it crucial for radar cabling.
During these years, methods to derive other useful products from polyethylene, including PE WAX (Polyethylene Wax), were also explored.

1950s:
The post-war era saw a significant boom in the plastics industry.
There was a widespread realization of the multiple benefits and applications of polyethylene-derived products.
PE WAX (Polyethylene Wax) started gaining prominence as an industrial lubricant, plastic processing aid, and in the cosmetics industry.

1970s and 1980s:
With advancements in refining and polymer processing techniques, more types and grades of PE WAX (Polyethylene Wax) became available.
Oxidized and functionalized PE WAX (Polyethylene Wax) emerged, catering to diverse industry needs.

1990s to Present:
The applications of PE WAX (Polyethylene Wax) diversified further.
Today, PE WAX (Polyethylene Wax)not just limited to industrial and cosmetic applications.
PE WAX (Polyethylene Wax)’s used in a myriad of products, from inks to coatings, textiles, and beyond.

Environmental considerations have also led to efforts to produce more sustainable and eco-friendly PE WAX (Polyethylene Wax) variants.
The journey of PE WAX (Polyethylene Wax) mirrors that of the larger polymer and petrochemical industries.
As technology and scientific understanding have grown, so have the applications and varieties of this versatile product.



PE WAX (POLYETHYLENE WAX) OTHER NAMES:
Polyethylene Wax (PE Wax) is known in the industry and market by various names, often based on its specific applications, properties, or even based on branding by manufacturers.
Here are some of its commonly recognized names and terms associated with it:

*Polyethylene Homopolymer Wax:
This term is more technical and elaborates on its chemical nature, specifying that it is a homopolymer derived from ethylene.

*PE WAX (Polyethylene Wax):
A common abbreviation used in industries and commercial arenas.

*Polywax:
Often used as a generic term for polyethylene-based waxes.

*Fischer-Tropsch Waxes:
Although not strictly PE WAX (Polyethylene Wax), these waxes are sometimes confused with or categorized alongside PE WAX (Polyethylene Wax) because of their similar appearance and properties.

*Low Molecular Weight Polyethylene (LMWPE):
This refers to the fact that PE WAX (Polyethylene Wax) is derived from polyethylene with a low molecular weight.

*Ethene Homopolymer Wax:
Another term reflecting its chemical lineage.



PHYSICAL and CHEMICAL PROPERTIES of PE WAX (POLYETHYLENE WAX):
CAS NUMBER: 9002-88-4
CHEMICAL NAME: Pe Wax, Pe Wax, Polyethylene Wax, Polyethylene Wax, Homopolymer
MELTING POINT: 107 °C -121 °C
BOILING POINT:173.89 °C
VISCOSITY: < 300 mPas
FLASH POINT: > 193 °C (CC)
MELT VISCOSITY (140 °C) cps: 40-60
PENETRATION DMM: < 5
DENSITY g/ml: 0.95
Density: 0.92±0.03
Appearance: Flake/Pearl
Melting Point: 100±10
Color: White
Solubility in Water: Insoluble
Volatile (%): Max 2
Drop Melting Point: 90 – 95° C
Melting Point: 100 – 110° C
Flash Point: 135° c
Density@ 20°c: 0.9 ± 0.02 KG/m3
Oil Content: 0.5 -1 %
Viscosity@ 140°c: 28.5 – 33.4 c.st
Moisture: 1.1 %
Penetration @ 25° c: 0.02 – 0.05 mm
Appearance: White Flake (Super Dry)



FIRST AID MEASURES of PE WAX (POLYETHYLENE WAX):
-Description of first-aid measures:
*If inhaled:
If breathed in, move person into fresh air.
*In case of skin contact:
Wash off with soap and plenty of water.
*In case of eye contact:
Flush eyes with water as a precaution.
*If swallowed:
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of PE WAX (POLYETHYLENE WAX):
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Keep in suitable, closed containers for disposal.



FIRE FIGHTING MEASURES of PE WAX (POLYETHYLENE WAX):
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available



EXPOSURE CONTROLS/PERSONAL PROTECTION of PE WAX (POLYETHYLENE WAX):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
*Body Protection:
Impervious clothing
*Respiratory protection:
Respiratory protection not required.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of PE WAX (POLYETHYLENE WAX):
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.



STABILITY and REACTIVITY of PE WAX (POLYETHYLENE WAX):
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available


PEANUT (ARACHIS HYPOGAEA L.) EXTRACT
Peanut Extract, derived from the seeds of Arachis hypogaea L., is known for its moisturizing, antioxidant, and emollient properties.
Peanut Extract is widely recognized for its ability to nourish the skin, protect against oxidative stress, and provide rich hydration, making it a valuable ingredient in skincare and cosmetic formulations.
This versatile extract offers both therapeutic and cosmetic benefits, helping to maintain skin hydration, promote elasticity, and protect against environmental damage.

CAS Number: 8002-03-7
EC Number: 232-296-4

Synonyms: Peanut Extract, Arachis hypogaea Extract, Peanut Oil Extract, Groundnut Extract, Arachis Extract, Peanut Seed Extract, Groundnut Oil Extract, Peanut Seed Phytocomplex, Arachis Oil Extract, Groundnut Bioactive Extract



APPLICATIONS


Peanut Extract is extensively used in skincare products for its moisturizing properties, providing deep hydration and nourishment for dry skin.
Peanut Extract is favored in the formulation of antioxidant creams, where it helps protect the skin from oxidative stress and environmental damage.
Peanut Extract is utilized in the development of emollient lotions, offering soothing and softening benefits for rough or irritated skin.

Peanut Extract is widely used in the creation of anti-aging creams, providing benefits for improving skin elasticity and reducing the appearance of fine lines.
Peanut Extract is employed in the formulation of hydrating body butters, offering long-lasting moisture and skin protection.
Peanut Extract is essential in the production of lip balms, where it helps to nourish and protect dry, chapped lips.

Peanut Extract is utilized in the production of rich moisturizing creams, offering hydration and protection for sensitive or dry skin.
Peanut Extract is a key ingredient in the creation of nourishing hand creams, providing hydration and protection for dry, rough hands.
Peanut Extract is used in the development of scalp treatments, providing moisture and care for dry or flaky scalps.

Peanut Extract is applied in the formulation of hair conditioners, where it helps to hydrate and nourish hair, improving its softness and manageability.
Peanut Extract is employed in the production of hair oils, offering hydration and shine for dry and damaged hair.
Peanut Extract is used in the development of soothing bath oils, providing moisture and relaxation for dry or irritated skin.

Peanut Extract is widely utilized in the formulation of emollient creams, offering protective and moisturizing care for sensitive skin.
Peanut Extract is a key component in the creation of foot creams, providing deep hydration and nourishment for rough, cracked feet.
Peanut Extract is used in the production of after-sun care products, offering soothing hydration for sun-exposed skin.

Peanut Extract is employed in the formulation of massage oils, where it helps to hydrate the skin and improve elasticity.
Peanut Extract is applied in the development of anti-inflammatory creams, providing soothing and nourishing care for irritated or inflamed skin.
Peanut Extract is utilized in the creation of baby care products, offering gentle hydration and protection for delicate skin.

Peanut Extract is found in the formulation of moisturizing face masks, providing deep hydration and nourishment for dry, dull skin.
Peanut Extract is used in the production of lip care products, offering moisture and protection for dry, chapped lips.
Peanut Extract is a key ingredient in moisturizing shampoos, providing hydration and care for dry or damaged hair.



DESCRIPTION


Peanut Extract, derived from the seeds of Arachis hypogaea L., is known for its moisturizing, antioxidant, and emollient properties.
Peanut Extract is widely recognized for its ability to nourish the skin, protect against oxidative stress, and provide rich hydration, making it a valuable ingredient in skincare and cosmetic formulations.

Peanut Extract offers additional benefits such as improving skin elasticity, soothing irritation, and promoting overall skin health.
Peanut Extract is often incorporated into formulations designed to hydrate and protect the skin from environmental stressors while maintaining its softness and suppleness.
Peanut Extract is recognized for its ability to enhance skin hydration, promoting long-lasting moisture and protection against dryness.

Peanut Extract is commonly used in both traditional and innovative skincare formulations, providing a reliable solution for maintaining skin hydration and protection.
Peanut Extract is valued for its ability to support the skin's natural barrier function, making it a key ingredient in products that aim to improve skin texture and resilience.
Peanut Extract is a versatile ingredient that can be used in a variety of products, including creams, lotions, oils, and hair care treatments.

Peanut Extract is an ideal choice for products targeting skin hydration, nourishment, and protection, providing natural and effective care for dry, sensitive, or aging skin.
Peanut Extract is known for its compatibility with other moisturizing and antioxidant ingredients, allowing it to be easily integrated into multi-functional formulations.
Peanut Extract is often chosen for formulations requiring a balance between hydration, skin protection, and antioxidant care, ensuring comprehensive skin health benefits.

Peanut Extract enhances the overall effectiveness of skincare products by providing natural support for skin hydration, elasticity, and protection.
Peanut Extract is a reliable ingredient for creating products that offer noticeable improvements in skin texture, softness, and moisture retention.
Peanut Extract is an essential component in innovative skincare products known for their performance, safety, and ability to support healthy, hydrated skin.



PROPERTIES


Chemical Formula: N/A (Natural extract)
Common Name: Peanut Extract (Arachis hypogaea Extract)
Molecular Structure:
Appearance: Light yellow to brown oil or powder
Density: Approx. 0.90-0.95 g/cm³ (for oil extract)
Melting Point: N/A (oil form)
Solubility: Soluble in oils; insoluble in water
Flash Point: >250°C (for oil extract)
Reactivity: Stable under normal conditions; no known reactivity issues
Chemical Stability: Stable under recommended storage conditions
Storage Temperature: Store between 15-25°C in a cool, dry place
Vapor Pressure: Low (for oil extract)



FIRST AID


Inhalation:
If Peanut Extract is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Wash the affected area with soap and water.
If skin irritation persists, seek medical attention.

Eye Contact:
In case of eye contact, flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
If Peanut Extract is ingested, do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:

Personal Protection:
Wear appropriate personal protective equipment (PPE) such as gloves and safety goggles if handling large quantities.
Use in a well-ventilated area to avoid inhalation of vapors or dust.

Ventilation:
Ensure adequate ventilation when handling large amounts of Peanut Extract to control airborne concentrations below occupational exposure limits.

Avoidance:
Avoid direct contact with eyes and prolonged skin contact.
Do not eat, drink, or smoke while handling Peanut Extract.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Contain spills to prevent further release and minimize exposure.
Absorb with inert material (e.g., sand, vermiculite) and collect for disposal.
Dispose of in accordance with local regulations.

Storage:
Store Peanut Extract in a cool, dry, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid inhalation of vapors or direct contact with skin and eyes.
Use explosion-proof equipment in areas where vapors may be present.
PEANUT FLAVOR
cas no 9000-69-5 Poly-D-galacturonic acid methyl ester;
PECEOL ISOSTEARIQUE
DESCRIPTION:

Peceol Isostearique Consists of mono-, di- and triglycerides of oleic (C18:1) acid, the monoester fraction being predominant
Peceol Isostearique is Solubilizer for lipophilic APIs and bioavailability enhancer.
Peceol Isostearique is Oily vehicle containing long-chain fatty acids (C18:1) for LFCS Type I (oily), Type II (SEDDS), and Type III (SMEDDS), associated with lymphatic absorption.



CAS: 61788-61-2


CHEMICAL AND PHYSICAL CHARACTERISTICS OF PECEOL ISOSTEARIQUE:
Product form
Liquid
Viscosity (mPa.s)
220 (20°C)
HLB
1
Composition:
Consists of mono-, di- and triglycerides of oleic (C18:1) acid, the monoester fraction being predominant, Glyceryl monooleate (type 40) NF

Dosage Form:
Oral, Soft and hard gelatin capsule filling., Topical, Topical emulgel and ointment.

Function:
Oily vehicle containing long-chain fatty acids (C18:2) for LFCS Type I (oily), Type II (SEDDS), and Type III (SMEDDS), associated with lymphatic absorption.
Oily vehicle for topical formulations.
Solubilizer for lipophilic APIs and bioavailability enhancer.




Peceol Isostearique is Oily vehicle for topical formulations.
Safety of use is inferred by GRAS status and precedence of use in approved pharmaceutical products.


SAFETY INFORMATION ABOUT PECEOL ISOSTEARIQUE
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product.



PECEOL ISOSTEARIQUE = GLYCEROL MONOISOSTEARATE
Peceol Isostearique = Glycerol monoisostearate is a hygroscopic, white, odorless and sweet-tasting flaky powder.
Peceol Isostearique = Glycerol monoisostearate is the glycerol ester of stearic acid.


CAS Number: 66085-00-5
EC Number: 266-124-4
MDL Number: MFCD00152509
INCI/Chemical Name: Glyceryl Isostearate
Molecular Formula : C21H42O4



SYNONYMS:
Isooctadecanoicacid,monoesterwith1,2,3-propanetriol, Isostearicacid,1,2,3-propaneriolester(1:1), GLYCEROL MONOISOSTEARATE, isooctadecanoic acid, monoester with glycerol, ALPHA-MONOISOSTEARYLGLYCERYLETHER, Isooctadecansure, Monoester mit Glycerin, Glyceroisoste, Imwitor-780K, Einecs 266-124-4, Glyceroisostearate, GLYCEROL MONOISOSTEARATE, ALPHA-MONOISOSTEARYLGLYCERYLETHER, Isooctadecansure, Monoester mit Glycerin, Isostearicacid,1,2,3-propaneriolester(1:1), isooctadecanoic acid, monoester with glycerol, Isooctadecanoicacid, monoesterwith1,2,3-propanetriol, Isooctadecanoicacid, monoesterwith1,2,3-propanetriol, Isostearicacid,1,2,3-propaneriolester(1:1), GLYCEROL MONOISOSTEARATE, isooctadecanoic acid, monoester with glycerol, ALPHA-MONOISOSTEARYLGLYCERYLETHER, Isooctadecansure, Monoester mit Glycerin, Glyceroisostearate, Imwitor-780K, Emerest 2410, 2,3-Dihydroxypropyl 16-methylheptadecanoate, Glycerol monoisostearate, Glyceryl monoisostearate, GLYCERYL ISOSTEARATE, 66085-00-5, 50486-18-5, HYE7O27HAO, 67938-24-3, Isooctadecanoic acid, monoester with 1,2,3-propanetriol, AKD-2A, Isostearic acid, 1,2,3-propaneriol ester (1:1), Isooctadecanoic acid, monoester with glycerol, 2,3-Dihydroxypropyl isooctadecanoate, UNII-HYE7O27HAO, EINECS 256-603-6, EINECS 266-124-4, EINECS 267-822-1, MGIS, NIKKOL MGIS, glycerin monoisostearate, GLYCEROISOSTEARATE, EC 266-124-4, PRISORINE 2040, PRISORINE GMIS 2040, SCHEMBL2516961, DTXSID70867203, GLYCERYL ISOSTEARATE [II], ISOSTEARIC ACID MONOGLYCERIDE, glycerol monoisostearate, AldrichCPR, 2,3-Dihydroxypropyl16-methylheptadecanoate, DS-016296, NS00004917, Q27280163



Peceol Isostearique = Glycerol monoisostearateis a glycerin monoisostearate ester, a highly substantive, rich, liquid emollient derived from isostearic acid.
Peceol Isostearique = Glycerol monoisostearate offers low HLB emulsifying properties and provides soft conditioning, good moisturization, and excellent spreading in liquid personal wash applications.


Peceol Isostearique = Glycerol monoisostearate is recommended for use in personal care and cosmetic formulations.
Peceol Isostearique = Glycerol monoisostearate is a natural product found in Streptomyces albidoflavus with data available.
Peceol Isostearique = Glycerol monoisostearate is an organic molecule used as an emulsifier.


Peceol Isostearique = Glycerol monoisostearate is a hygroscopic, white, odorless and sweet-tasting flaky powder.
Peceol Isostearique = Glycerol monoisostearate is the glycerol ester of stearic acid.
Pancreatic lipase naturally breaks down fat in the body and is found in fatty foods.


Peceol Isostearique = Glycerol monoisostearate, used as an emulsifier in ice cream, prevents the development of coarse ice crystals and gives a smooth texture.
Peceol Isostearique = Glycerol monoisostearate, which enables the formation of stable emulsions that do not break down during freezing, improves the shelf life by keeping the ice cream firm and dry without hardening.


Peceol Isostearique = Glycerol monoisostearate, which facilitates the control of the aeration process for optimum overrun, should be added to the mixture at a rate of 0.3-0.4% before homogenization and pasteurization.


Peceol Isostearique = Glycerol monoisostearate in bakery products such as bread and cake; It causes the formation of a soft, moist product interior with a good pore structure, gives white shine and volume to the products, retains moisture, delays the spongy structure and staling, and increases the shelf life of the product.


Unlock the versatile potential of Peceol Isostearique = Glycerol monoisostearate, a highly refined and multifunctional chemical compound that offers a wealth of applications across diverse industries.
This CAS-numbered compound, 66085-00-5, is a true gem in the world of specialty chemicals, boasting a unique combination of properties that make Peceol Isostearique = Glycerol monoisostearate an indispensable tool for researchers, formulators, and innovators alike.


At its core, Peceol Isostearique = Glycerol monoisostearate is a complex ester derived from the esterification of glycerol and isostearic acid.
This intricate molecular structure endows the compound with a remarkable array of characteristics, making Peceol Isostearique = Glycerol monoisostearate a valuable asset in a wide range of applications.


With a purity of at least 95%, Peceol Isostearique = Glycerol monoisostearate ensures consistent and reliable performance, allowing you to push the boundaries of your research and development efforts.
The versatility of Peceol Isostearique = Glycerol monoisostearate is truly astounding.


In the realm of personal care and cosmetic formulations, Peceol Isostearique = Glycerol monoisostearate shines as a multifunctional ingredient, serving as an emulsifier, emollient, and skin-conditioning agent.
Its ability to enhance the stability, texture, and sensorial properties of a wide range of products, from lotions and creams to gels and serums, makes Peceol Isostearique = Glycerol monoisostearate an indispensable tool for cosmetic chemists and formulators.



USES and APPLICATIONS of PECEOL ISOSTEARIQUE = GLYCEROL MONOISOSTEARATE:
Peceol Isostearique = Glycerol monoisostearatealso provides moisturizing properties that make it ideal for AP/DEO and rich hand and body creams.
Peceol Isostearique = Glycerol monoisostearate has been shown to promote film formation in skin care applications.
Thanks to its pigment-dispersing properties, Peceol Isostearique = Glycerol monoisostearate is used in decorative cosmetics.


Peceol Isostearique = Glycerol monoisostearate is a safe and eco-friendly ingredient.
Peceol Isostearique = Glycerol monoisostearate is cold-processable, vegetable-derived, and biodegradable.
Peceol Isostearique = Glycerol monoisostearate is used in moisturizers, creams, and other facial and body care products.


Cosmetic Uses of Peceol Isostearique = Glycerol monoisostearate: skin conditioning - emollient, and surfactant - emulsifying
Peceol Isostearique = Glycerol monoisostearate is used as both emulsifier and stabilizer in the food industry.
Peceol Isostearique = Glycerol monoisostearate is available in powder or bead forms in the market.


Peceol Isostearique = Glycerol monoisostearate is a food additive that has a unique odor and is white or sometimes beige in color and is known in the food industry with the food code e 471.
Peceol Isostearique = Glycerol monoisostearate is a very effective emulsifier in emulsifying the oil - water phase.


Peceol Isostearique = Glycerol monoisostearate is also effective in extending the stratification and shelf life of food products.
Peceol Isostearique = Glycerol monoisostearate is especially used in the bread, bakery and pastry industry and the oil industry.
Apart from the food industry, Peceol Isostearique = Glycerol monoisostearate is used in the cosmetics, detergent, plastic and pharmaceutical industries.


Peceol Isostearique = Glycerol monoisostearate is added to the formulations of ice cream, starch products, dairy products, chewing gum, chocolate and other food products.
Peceol Isostearique = Glycerol monoisostearate is used as a softener in textile products and as a lubricant in plastic products.


With the use of Peceol Isostearique = Glycerol monoisostearate, the amount of egg yolk used in the products decreases, thus reducing the cost.
In chocolate products, Peceol Isostearique = Glycerol monoisostearate provides a good oil dispersion even at high temperatures, reduces stickiness and separation during production and storage, improves texture and consistency, reduces crystallization of sugar, reduces blooming and loss of product-specific shine, prevents products such as caramel and nougat from falling on the teeth, prevents aroma substances from falling on the teeth.


Peceol Isostearique = Glycerol monoisostearate ensures better dispersion and stabilization and acts as a plasticizer in chewing gums.
In margarine products, Peceol Isostearique = Glycerol monoisostearate reduces the tension at the oil and water interfaces, which leads to the formation of stable emulsions.


When used with soy lecithin, the solubility of Peceol Isostearique = Glycerol monoisostearate increases.
Peceol Isostearique = Glycerol monoisostearate, which causes a better mouthfeel in the product and increases its spreadability properties, emulsifies the water in margarine and stabilizes the water in the oil.


Peceol Isostearique = Glycerol monoisostearate is a PEG-free emulsifier.
Peceol Isostearique = Glycerol monoisostearate is used to formulate cocoon dream cream.
Peceol Isostearique = Glycerol monoisostearate is an ester that functions as both an emulsifier and an emollient in creams and lotions.


Peceol Isostearique = Glycerol monoisostearate helps to simplify processing by allowing for cold process emulsification.
Peceol Isostearique = Glycerol monoisostearate produces less soaping than its straight-chain analogue.
Peceol Isostearique = Glycerol monoisostearate is a natural product found in Streptomyces albidoflavus with data available.


Peceol Isostearique = Glycerol monoisostearate is a food additive used as a thickener, emulsifier, anti-caking and preservative; an emulsifying agent for oils, waxes and solvents; a protective coating for hygroscopic dusts; a solidifying and control releasing agent in pharmaceuticals; and a resin lubricant.
Peceol Isostearique = Glycerol monoisostearate is also used in cosmetics and hair care products.


Peceol Isostearique = Glycerol monoisostearate is largely used in cooking preparations to add “body” to food.
Peceol Isostearique = Glycerol monoisostearate is responsible for giving ice cream and whipped cream their soft texture.
Peceol Isostearique = Glycerol monoisostearate is sometimes used as an anti-snake agent in breads.


Liquid emulsifier Peceol Isostearique = Glycerol monoisostearate is used as emollients, emulsifiers, thickeners, stabilizers, opacifiers and pearlescent agents.
Peceol Isostearique = Glycerol monoisostearate is used emulsions for skin and hair care products


Boasting a molecular formula of C21H42O4 and a molecular weight of 358.6 g/mol, Peceol Isostearique = Glycerol monoisostearate offers a wealth of applications in various industries.
Crafted with meticulous attention to detail, Peceol Isostearique = Glycerol monoisostearate's unique properties make it an indispensable tool for your chemical needs.


Explore its potential and unlock new possibilities in your research, formulations, or manufacturing processes.
Beyond the personal care industry, Peceol Isostearique = Glycerol monoisostearate finds its way into the world of food and nutrition.
As a food-grade emulsifier, Peceol Isostearique = Glycerol monoisostearate plays a crucial role in stabilizing and improving the texture of various food products, from baked goods and confections to dairy items and sauces.


Its versatility allows Peceol Isostearique = Glycerol monoisostearate to seamlessly integrate into a multitude of culinary applications, catering to the ever-evolving demands of the modern food industry.
In the realm of industrial applications, Peceol Isostearique = Glycerol monoisostearate demonstrates its prowess as a lubricant, release agent, and plasticizer.


Its unique chemical structure allows Peceol Isostearique = Glycerol monoisostearate to impart desirable properties to a diverse range of materials, from polymers and coatings to inks and adhesives.
Peceol Isostearique = Glycerol monoisostearate's ability to enhance performance, reduce friction, and improve processability makes it a valuable asset in the manufacturing and engineering sectors.



FEATURES OF PECEOL ISOSTEARIQUE = GLYCEROL MONOISOSTEARATE:
*Highly refined and purified compound with a minimum purity of 95%
*Derived from the esterification of glycerol and isostearic acid
*Multifunctional properties as an emulsifier, emollient, and skin-conditioning agent
*Versatile applications of Peceol Isostearique = Glycerol monoisostearate in personal care, food, and industrial formulations
*Peceol Isostearique = Glycerol monoisostearate enhances stability, texture, and sensorial properties of a wide range of products
*Peceol Isostearique = Glycerol monoisostearate serves as a lubricant, release agent, and plasticizer in various industrial applications
*Peceol Isostearique = Glycerol monoisostearate complies with relevant regulatory standards and guidelines



FUNCTIONS OF PECEOL ISOSTEARIQUE = GLYCEROL MONOISOSTEARATE:
*Emollient
*Emulsifier



PHYSICAL and CHEMICAL PROPERTIES of PECEOL ISOSTEARIQUE = GLYCEROL MONOISOSTEARATE:
CAS RN: 66085-00-5
Molecular Formula: C21H42O4
Molecular Weight: 358.56
Alternate Name(s): Emerest 2410
Classification: Surfactant
Molecular Formula: C21H42O4
Molecular Weight: 358.56
CAS No: [66085-00-5]
Product Code: RCA08500
MOL file: Download
Chemical Formula: C21H42O4
Molecular Weight: 358.6 g/mol
Smiles: CC(C)CCCCCCCCCCCCCCC(=O)OCC(CO)O
Molecular Weight: 358.6 g/mol

XLogP3: 7.1
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 19
Exact Mass: 358.30830982 g/mol
Monoisotopic Mass: 358.30830982 g/mol
Topological Polar Surface Area: 66.8Ų
Heavy Atom Count: 25
Formal Charge: 0
Complexity: 292
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 1
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0

Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 481.00 to 482.00 °C @ 760.00 mm Hg (estimated)
Flash Point: 309.00 °F TCC (153.80 °C) (estimated)
logP (o/w): 7.274 (estimated)
Soluble in water: 0.01421 mg/L @ 25 °C (estimated)
CAS Number: 66085-00-5
Ref #: 3D-RCA08500
Purity: Min. 95%
Chemical Formula: C21H42O4
Molecular Weight: 358.6 g/mol
HS Code: 2915907098

Name: GLYCEROL MONOISOSTEARATE
CAS: 66085-00-5
EINECS(EC#): 266-124-4
Molecular Formula: C21H42O4
MDL Number: MFCD00152509
Molecular Weight: 358.56
Odor: Mild waxy odor at 100.00%
LogP: 7.274 (estimated)
EPA Substance Registry System: Glycerol monoisostearate (66085-00-5)
IUPAC Name: 2,3-dihydroxypropyl 16-methylheptadecanoate
Solubility in water: 0.01421 mg/L @ 25 °C (estimated)
Boiling Point: 481.5°C at 760 mmHg

Density: 0.957 g/cm3
InChI Key: ASKIVFGGGGIGKH-UHFFFAOYSA-N
InChI: InChI=1S/C21H42O4/c1-19(2)15-13-11-9-7-5-3-4-6-8-10-12-14-16-21(24)25-18-20(23)17-22/h19-20,22-23H,3-18H2,1-2H3
Canonical SMILES: CCC(C)CCCCCCCCCCCCC(=O)OCC(CO)O
Refractive Index: 1.468
CBNumber: Not specified
FDA UNII: HYE7O27HAO
EPA Substance Registry System: Glycerol monoisostearate (66085-00-5)
CAS Registry Number: 66085-00-5
Molecular Weight: 358.56
EINECS: 266-124-4



FIRST AID MEASURES of PECEOL ISOSTEARIQUE = GLYCEROL MONOISOSTEARATE:
-Description of first-aid measures:
*General advice:
Consult a physician.
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
If breathed in, move person into fresh air.
Consult a physician.
*In case of skin contact:
Wash off with soap and plenty of water.
Consult a physician.
*In case of eye contact:
Flush eyes with water as a precaution.
*If swallowed:
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of PECEOL ISOSTEARIQUE = GLYCEROL MONOISOSTEARATE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Pick up and arrange disposal without creating dust.
Sweep up and shovel.
Keep in suitable, closed containers for disposal.



FIRE FIGHTING MEASURES of PECEOL ISOSTEARIQUE = GLYCEROL MONOISOSTEARATE:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available



EXPOSURE CONTROLS/PERSONAL PROTECTION of PECEOL ISOSTEARIQUE = GLYCEROL MONOISOSTEARATE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
Choose body protection
*Respiratory protection:
Respiratory protection is not required.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of PECEOL ISOSTEARIQUE = GLYCEROL MONOISOSTEARATE:
-Precautions for safe handling:
*Hygiene measures:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.



STABILITY and REACTIVITY of PECEOL ISOSTEARIQUE = GLYCEROL MONOISOSTEARATE:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available


PECEOL ISOSTEARIQUE = GLYCEROL MONOISOSTEARATE
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is a self emulsifying wax.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is located in dozens of personal care products, including moisturizers, eye cream, sunscreen, makeup and hand creams.
Direct Chems provide PECEOL ISOSTEARIQUE = Glycerol monoisostearate which is self emulsifying in pearl form and can be used as a viscosity enhancer adding emollient properties which makes skin softer and supple.

CAS: 123-94-4
MF: C21H42O4
MW: 358.56
EINECS: 204-664-4

Synonyms
DL-ALPHA-STEARIN;EMALEX GMS-10SE;EMALEX GMS-195;EMALEX GMS-15SE;EMALEX GMS-B;EMALEX GMS-ASE;EMALEX GMS-A;EMALEX GMS-55FD;Glyceryl monostearate;123-94-4;Monostearin;31566-31-1;GLYCEROL MONOSTEARATE;Glyceryl stearate;Tegin;1-Stearoyl-rac-glycerol;2,3-dihydroxypropyl octadecanoate;1-MONOSTEARIN;Glycerin 1-monostearate;Glycerol 1-monostearate;Glycerol 1-stearate;Stearin, 1-mono-;Stearic acid 1-monoglyceride;1-Glyceryl stearate;Glycerin 1-stearate;Sandin EU;1-Monostearoylglycerol;Octadecanoic acid, 2,3-dihydroxypropyl ester;Aldo MSD;Aldo MSLG;Glyceryl 1-monostearate;Stearoylglycerol;alpha-Monostearin;Tegin 55G;Emerest 2407;Aldo 33;Aldo 75;Glycerin monostearate;Arlacel 165;3-Stearoyloxy-1,2-propanediol;Cerasynt SD;11099-07-3;2,3-Dihydroxypropyl stearate;.alpha.-Monostearin;Monoglyceryl stearate;Glycerol alpha-monostearate;Cefatin;Dermagine;Monelgin;Sedetine;Admul;Orbon;Citomulgan M;DrewmulseV;Cerasynt S;Drewmulse TP;Tegin 515;Cerasynt SE;Cerasynt WM;Cyclochem GMS;Drumulse AA;Protachem GMS;Witconol MS;Witconol MST;FEMA No. 2527;Glyceryl stearates;Monostearate (glyceride);Stearin, mono-;Unimate GMS;Glyceryl monooctadecanoate;Ogeen M;Emcol CA;Emcol MSK;Hodag GMS;Ogeen GRB;Ogeen MAV;Aldo MS;Aldo HMS;Armostat 801;Kessco 40;Stearic monoglyceride;Abracol S.L.G.;Arlacel 161;Arlacel 169;Imwitor 191;Imwitor 900K;NSC 3875;Atmul 67;Atmul 84;Starfol GMS 450;Starfol GMS 600;Starfol GMS 900;Cerasynt 1000-D;Emerest 2401;Aldo-28;Aldo-72;Atmos 150;Atmul 124;Estol 603;Ogeen 515;Tegin 503;Grocor 5500;Grocor 6000;Glycerol stearate, pure;Stearic acid alpha-monoglyceride;Cremophor gmsk;Glyceryl 1-octadecanoate;Cerasynt-sd;Lonzest gms;Cutina gms;Lipo GMS 410;Lipo GMS 450;Lipo GMS 600;glycerol stearate;1-MONOSTEAROYL-rac-GLYCEROL;Nikkol mgs-a;Glyceryl monopalmitostearate;USAF KE-7;1-octadecanoyl-rac-glycerol;EMUL P.7;22610-63-5;EINECS 204-664-4;EINECS 245-121-1;Stearic acid, monoester with glycerol;Glycerol .alpha.-monostearate;Glyceroli monostearas;Glycerol monostearate, purified;Imwitor 491;Sorbon mg-100;Cithrol gms 0400;UNII-258491E1RZ;NSC3875;Stearic acid .alpha.-monoglyceride;(1)-2,3-Dihydroxypropyl stearate;MONOSTEARIN (L);NSC-3875;1-Monooctadecanoylglycerol;EINECS 250-705-4;1,2,3-Propanetriol monooctadecanoate;Octadecanoic acid, ester with 1,2,3-propanetriol;GLYCERYL 1-STEARATE;AI3-00966;MG(18:0/0:0/0:0)[rac];85666-92-8;DTXSID7029160;CHEBI:75555;1-Stearoyl-rac-glycerol (90%);EC 250-705-4

PECEOL ISOSTEARIQUE = Glycerol monoisostearate also acts as a fast penetrating emollient which helps retain hydration, lubricate, condition and soften skin.
They slow loss of moisture so is ideal when adding to natural formulations.
The presence of PECEOL ISOSTEARIQUE = Glycerol monoisostearate enables other ingredients in the formulation to continue functioning effectively in order to excel their beneficial properties by extending shelf life, preventing products from freezing and developing crusts on the surface.
One important factor is PECEOL ISOSTEARIQUE = Glycerol monoisostearate allows oils to be added to products but decreases the greasiness so the final product is a smooth, creamy texture.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is a long chain molecule typically occurring in the body as a by-product of the breakdown of fats.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is one of the panels of serum metabolic biomarkers for detecting and diagnosing cancer, especial ovarian cancer.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is also used in the development of drug delivery vehicles such as nanoparticles and microemulsions.

PECEOL ISOSTEARIQUE = Glycerol monoisostearate can also be used as an emulsifying agent, which allows the suspension of pharmaceuticals in a biodegradable form.
A rac-1-monoacylglycerol composed of equal amounts of 3-stearoyl-sn-glycerol and 1-stearoyl-sn-glycerol.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate, commonly known as GMS, is a monoglyceride commonly used as an emulsifier in foods.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate takes the form of a white, odorless, and sweet-tasting flaky powder that is hygroscopic.
Chemically PECEOL ISOSTEARIQUE = Glycerol monoisostearate is the glycerol ester of stearic acid.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is also used as hydration powder in exercise formulas
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is a compound commonly used as a food additive and in various industrial applications.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is a type of monoglyceride, which is a molecule composed of glycerol linked to a single fatty acid, in this case, stearic acid.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is known for its emulsifying properties, which make it useful in food production, cosmetics, and pharmaceuticals .

PECEOL ISOSTEARIQUE = Glycerol monoisostearate Chemical Properties
Melting point: 78-81 °C
Boiling point: 476.9±25.0 °C(Predicted)
Density: 0.9678 g/cm3
FEMA: 2527 | GLYCERYL MONOSTEARATE
Storage temp.: -20°C
Solubility: Chloroform (Slightly)
Form: Solid
pka: 13.16±0.20(Predicted)
Color: White to Off-White
Odor: at 100.00 %. mild fatty waxy
Odor Type: fatty
JECFA Number: 918
Merck: 4489
BRN: 1728685
Hydrophilic-Lipophilic Balance (HLB): 5.5
Dielectric constant: 4.9(77.0℃)
InChIKey: VBICKXHEKHSIBG-UHFFFAOYSA-N
LogP: 7.23
CAS DataBase Reference:123-94-4(CAS DataBase Reference)
NIST Chemistry Reference: PECEOL ISOSTEARIQUE = Glycerol monoisostearate (123-94-4)
EPA Substance Registry System: PECEOL ISOSTEARIQUE = Glycerol monoisostearate (123-94-4)

The physical and chemical properties of PECEOL ISOSTEARIQUE = Glycerol monoisostearate have been extensively studied.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate's effects on the physico-chemical, thermal, and rheological properties of corn and potato starches were investigated, showing that GMS can modify the swelling power, solubility, and syneresis of starches.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate also affected the transition temperatures and enthalpy of gelatinization, as well as the textural properties of noodles made from these starches.
In another study, the stability of the α-gel phase of a PECEOL ISOSTEARIQUE = Glycerol monoisostearate-water system was examined, revealing that intrinsic factors like co-emulsifiers and extrinsic factors like cooling rate and shear can influence the phase stability.
The effects of PECEOL ISOSTEARIQUE = Glycerol monoisostearate on the performance of thermoplastic starch were also explored, demonstrating its impact on melting point, degradation temperature, and moisture sorption .

Uses
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is self-emulsifying glyceryl stearate.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate provides a stable, uniform oil-in-water emulsion.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is used in the development of drug delivery vehicles such as nanoparticles and microemulsions.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is a food additive used as a thickening, emulsifying, anticaking, and preservative agent; an emulsifying agent for oils, waxes, and solvents; a protective coating for hygroscopic powders; a solidifier and control release agent in pharmaceuticals; and a resin lubricant.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is also used in cosmetics and hair-care products.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is largely used in baking preparations to add "body" to the food.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is somewhat responsible for giving ice cream and whipped cream their smooth texture.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is sometimes used as an antistaling agent in bread.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate can also be used as an additive in plastic, where GMS works as an antistatic and antifogging agent.

PECEOL ISOSTEARIQUE = Glycerol monoisostearate is common in food packaging.
Structure, synthesis, and occurrence
PECEOL ISOSTEARIQUE = Glycerol monoisostearate exists as three stereoisomers, the enantiomeric pair of 1-glycerol monostearate and 2-glycerol monostearate.
Typically these are encountered as a mixture as many of their properties are similar.
Commercial material used in foods is produced industrially by a glycerolysis reaction between triglycerides (from either vegetable or animal fats) and glycerol.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate occurs naturally in the body as a product of the breakdown of fats by pancreatic lipase.
PECEOL ISOSTEARIQUE = Glycerol monoisostearate is present at very low levels in certain seed oils.
PECTIN
Poly-D-galacturonic acid methyl ester; APPLE PECTIN;POLY-D-GALACTURONIC ACID METHYL ESTER;POLYGALACTURONIC ACID METHYL ESTER;PARTIALLY METHOXYLATED POLYGALACTURONIC ACID;PECTIN, FROM LEMON;PECTIN;PECTIN, APPLE;PECTIN, CITRUS CAS NO:9000-69-5
PEG 100 STEARATE
PEG 100 Stearate PEG 100 Stearate is a polyethylene glycol ester of stearic acid. PEG 100 Stearate functions as an effective emollient, emulsifier and surfactant. PEG 100 Stearate is used in facial cleansers, creams and lotions, shampoos. PEG 100 STEARATE is classified as : Surfactant CAS Number: 9004-99-3 COSING REF No: 77453 Chem/IUPAC Name: Poly(oxy-1,2-ethanediyl), .alpha.-(1-oxooctadecyl)-.omega.-hydroxy- (100 mol EO average molar ratio) What Is It? Polyethylene Glycol (PEG) Stearates (PEG-2 Stearate, PEG-6 Stearate, PEG-8 Stearate, PEG-12 Stearate, PEG-20 Stearate, PEG-32 Stearate, PEG-40 Stearate, PEG-50 Stearate, PEG 100 Stearate, PEG-150 Stearate) are esters of polyethylene glycol and stearic acid. The PEG Stearates are soft to waxy solids that are white to tan in color. In cosmetics and personal care products, PEG Stearates are used in skin creams, conditioners, shampoos, body cleansers and soapless detergents. Why is it used in cosmetics and personal care products? The PEG 100 Stearates clean the skin and hair by helping water to mix with oil and dirt so that they can be rinsed away. Scientific Facts: The PEG 100 Stearates are produced from stearic acid, a naturally occurring fatty acid. The numerical value of each PEG Stearate corresponds to the average number of ethylene oxide monomers in the polyethylene chain. Polyethylene glycol ingredients may also be named with a number that indicates molecular weight, for example polyethylene glycol (400) stearate is another name for PEG-8 Stearate. Why is PEG 100 Stearate in My Skincare Product? PEG or polyethylene glycol stearate is an ingredient that is used in skincare and body care products. PEG 100 stearate is a soft waxy substance used in moisturizers, conditioners, shampoos, cleansers, and soap-free detergents. The 100 in PEG 100 stearate refers to the number of ethylene oxide monomers present on the molecule. PEG 100 stearate is mainly utilized in your skincare products due to its emulsifying abilities. Emulsifiers help to mix oil and water-based ingredients so that they produce a smooth, stable texture. This emulsifying characteristic of PEG 100 stearate also helps to lift oil and dirt from the skin so that it can be rinsed away, making it a staple addition to cleansers and body washes. PEG 100 stearate is a PEG; PEGs are a class of ingredients that have been involved in controversy over their use, particularly from the clean or green beauty industry. This controversy is in part due to claims that it is linked to toxicity within the body due to the presence of impurities during the manufacturing process. This toxicity claim has been evaluated by both the US Food and Drug Administration (FDA) and the Cosmetic Ingredient Review Expert Panel, both of these groups are responsible for evaluation and regulation of skincare ingredients in the US. Through their research, they determined PEG compounds safe for their indicated uses in skincare and personal care products. In 2002 the Cosmetic Ingredient Review Expert Panel reviewed newly available data and reaffirmed the approval. However, if you are concerned, discuss PEG 100 Stearate with a doctor or dermatologist, who can advise you whether your medical history may place you at risk with this ingredient. THE GOOD:PEG 100 stearate is used as an emollient and a moisturizer THE NOT SO GOOD: WHO IS IT FOR?All skin types except those that have an identified allergy to it. SYNERGETIC INGREDIENTS:Works well with most ingredients KEEP AN EYE ON:Due to kidney issues associated with the use of PEG 100 stearate products on burn patients, it is recommended to not use PEG 100 stearate containing products on broken skin. Is PEG 100 Stearate Safe? Toxicity The safety of PEG compounds has been called into question in recent years. The questioning of the safety of this ingredient is due to toxicity concerns that result from impurities found in PEG compounds. The impurities of concern are ethylene oxide and 1,4 dioxane, both are by-products of the manufacturing process. Both 1,4 dioxane and ethylene oxide have been suggested to be linked with breast and uterine cancers. While these impurities may have been a concern previously, ingredient manufacturers and improved processes have eliminated the risk of impurities in the final product. The level of impurities that were found initially in PEG manufacturing was low in comparison to the levels proposed to be linked to cancers. Longitudinal studies or studies over a long period of use of PEG compounds have not found any significant toxicity or any significant impact on reproductive health. When applied topically, PEG 100 Stearate is not believed to pose significant dangers to human health. It doesn’t penetrate deeply into the skin and isn’t thought to have bioaccumulation concerns when used topically. Irritation Through research, PEG compounds have exhibited evidence that they are non-irritating ingredients to the eyes or the skin. This research used highly concentrated forms of the ingredient, concentrations that would not be found in your skincare products. The Cosmetic Ingredient Review Expert Panel found PEG compounds to be non-photosensitizing and non-irritating at concentrations up to 100%. However, despite the evidence suggesting that PEG compounds are non-irritating, some research has indicated that irritation can occur when the skin is broken or already irritated. In a study that was trialing the use of PEG containing antimicrobial cream on burn patients, some patients experienced kidney toxicity. The concentration of PEG compounds was identified to be the culprit. Given that there was no evidence of toxicity in any study of PEGs and intact skin, the Cosmetic Ingredient Review Expert Panel amended their safety guidelines to exclude the use of PEG containing products on broken or damaged skin. Is PEG 100 Stearate Vegan? Depending on the source of the stearic acid used to make PEG 100 stearate, it may be vegan. Most of the time, stearic acid is derived from plants. However, it can also be derived from animal origin. If it is of animal origin, the product has to comply with animal by-product regulation. Check with the brand you are thinking of using to determine whether their PEG 100 stearate is derived from a plant or animal source. Why Is PEG 100 Stearate Used? Emulsifier PEG 100 Stearate is included in skincare and beauty products for a variety of reasons, ranging from making the skin softer to helping product formulations better keep their original consistency. As an emollient, PEG 100 stearate is included within skincare product formulations to give the skin a softer feel. It achieves this through strengthening the skin’s moisture barrier by forming a thin fatty layer on the skin’s surface, which prevents moisture loss and increases overall hydration. This moisturizing effect increases the hydration of skin cells, which in turn makes the skin softer and boosts skin health. Texture Another use for PEG 100 stearate has to do with its emulsification properties. Emulsifiers are valued in the skincare and personal care industries because of their ability to mix water and oils. Without this ability, the oils in many formulations would begin to separate from the water molecules, thus undermining product texture and consistency. PEG 100 stearate is also used to help to cleanse through mixing oil and dirt so that it can be rinsed away. Surfactant Lastly, PEG 100 stearate can also act as a surfactant, when used in body and facial cleansers. Surfactants disrupt surface tension, helping to mix water and oil. This characteristic helps the ingredient cleanse the skin by mixing oil with water, lifting dirt trapped inside the skin’s oils, and rinsing it away from the skin. What Types of Products Contain PEG 100 Stearate? There are many products in the skin and personal care industry that are formulated with PEG 100 stearate because of its benefits to formulations and its relative safety. Facial cleansers, shampoos, lotions, and face creams have all been known to contain this ingredient. If you’ve had problems with this ingredient before, or if your doctor has advised you to stay away from PEG 100 stearate, it’s vital to read ingredient labels for any personal care product as it has many applications. What are PEGs? You have probably noticed that many of cosmetics and personal care products you use have different types of PEGs among ingredients. PEG, which is the abbreviation of polyethylene glycol, is not a definitive chemical entity in itself, but rather a mixture of compounds, of polymers that have been bonded together. Polyethylene is the most common form of plastic, and when combined with glycol, it becomes a thick and sticky liquid. PEGs are almost often followed by a number, for example PEG-6, PEG-8, PEG 100 and so on. This number represents the approximate molecular weight of that compound. Typically, cosmetics use PEGs with smaller molecular weights. The lower the molecular weight, the easier it is for the compound to penetrate the skin. Often, PEGs are connected to another molecule. You might see, for example, PEG 100 stearate as an ingredient. This means that the polyethylene glycol polymer with an approximate molecular weight of 100 is attached chemically to stearic acid. In cosmetics, PEGs function in three ways: as emollients (which help soften and lubricate the skin), as emulsifiers (which help water-based and oil-based ingredients mix properly), and as vehicles that help deliver other ingredients deeper into the skin. What effect do PEG 100 Stearate have on your skin? Polyethylene glycol compounds have not received a lot of attention from consumer groups but they should. The most important thing to know about PEGs is that they have a penetration enhancing effect, the magnitude of which is dependent upon a variety of variables. These include: both the structure and molecular weight of the PEG, other chemical constituents in the formula, and, most importantly, the overall health of the skin. PEGs of all sizes may penetrate through injured skin with compromised barrier function. So it is very important to avoid products with PEGs if your skin is not in best condition. Skin penetration enhancing effects have been shown with PEG-2 and PEG-9 stearate. This penetration enhancing effect is important for three reasons: 1) If your skin care product contains a bunch of other undesirable ingredients, PEGs will make it easier for them to get down deep into your skin. 2) By altering the surface tension of the skin, PEGs may upset the natural moisture balance. 3) PEG 100 Stearate are not always pure, but often come contaminated with a host of toxic impurities. Impurities and other PEG 100 Stearate risks According to a report in the International Journal of Toxicology by the cosmetic industry’s own Cosmetic Ingredient Review (CIR) committee, impurities found in various PEG compounds include ethylene oxide; 1,4-dioxane; polycyclic aromatic compounds; and heavy metals such as lead, iron, cobalt, nickel, cadmium, and arsenic. Many of these impurities are linked to cancer. PEG compounds often contain small amounts of ethylene oxide. Ethylene oxide (found in PEG-4, PEG-7, PEG4-dilaurate, and PEG 100) is highly toxic — even in small doses — and was used in World War I nerve gas. Exposure to ethylene glycol during its production, processing and clinical use has been linked to increased incidents of leukemia as well as several types of cancer. Finally, there is 1,4-dioxane (found in PEG-6, PEG-8, PEG-32, PEG-75, PEG-150, PEG-14M, and PEG-20M), which, on top of being a known carcinogen, may also combine with atmospheric oxygen to form explosive peroxides — not exactly something you want going on your skin. Even though responsible manufacturers do make efforts to remove these impurities (1,4-dioxane that can be removed from cosmetics through vacuum stripping during processing without an unreasonable increase in raw material cost), the cosmetic and personal care product industry has shown little interest in doing so. Surprisingly, PEG compounds are also used by natural cosmetics companies. If you find PEG 100 Stearate in your cosmetics… Although you might find conflicting information online regarding Polyethylene Glycol, PEGs family and their chemical relatives, it is something to pay attention to when choosing cosmetic and personal care products. If you have sensitive or damaged skin it might be a good idea to avoid products containing PEGs. Using CosmEthics app you can easy add PEGs to personal alerts. In our last blog post we wrote about vegan ingredients. Natural glycols are a good alternative to PEGs, for example natural vegetable glycerin can be used as both moisturiser and emulsifier. CosmEthics vegan list can help you find products that use vegetable glycerin as wetting agent. At present, there is not enough information shown on product labels to enable you to determine whether PEG compounds are contaminated. But if you must buy a product containing PEGs just make sure that your PEGs are coming from a respected brand. Glyceryl stearate and PEG 100 stearate is a combination of two emulsifying ingredients. The stabilising effect of both means that the product remains blended and will not separate. Description Glyceryl stearate is a solid and waxy compound. It is made by reacting glycerine (a soap by-product) with stearic acid (a naturally occurring, vegetable fatty acid). PEG 100 stearate is an off-white, solid ester of polyethylene glycol (a binder and a softener) and stearic acid. The surfactant qualities of glyceryl stearate and PEG 100 stearate allow oil and water to mix. Creams and lotions are water and oil droplets held together by materials called emulsifiers, without them oil droplets would float on top of the water. When used in a moisturiser, this forms a protective barrier on the surface of skin, greatly assisting moisture retention. Glyceryl Stearate (and) PEG 100 Stearate is a very versatile non-ionic oil-in-water emulsifier that creates silky smooth, ultra-light emulsions. Most datasheets I’ve seen state the content of each Glyceryl Stearate and PEG 100 Stearate as 48–52%, which averages out to a 50/50 blend, though check the datasheet from your supplier for the particular one you have. Appearance I’ve only seen it as brittle white flakes, but some manufacturers sell it as a powder or in pellets. Usage rate 1–25%, depending on the use. SEPPIC lists 5% for a fluid lotion, 10% for lotion, 15% for a thick lotion, 20% for a fluid cream, and 25% for a thick cream. Texture Brittle, hard; weightless in emulsions. Scent Nothing noticeable Absorbency Speed Very light Approximate Melting Point 50–60°C (122–140°F) pH 5.5–7 (3 % solution); tolerates a final pH range of approximately 4–9. Charge Non-ionic Solubility Oil Why do we use it in formulations? Glyceryl Stearate (and) PEG 100 Stearate is a very effective and crazy versatile emulsifier. It can be used to create everything from sprayable milks to ultra-thick emulsified body butters, and everything in between! Unlike emulsifying waxes like Polawax, Emulsifying Wax NF, Olivem 1000, and Ritamulse SCG, Glyceryl Stearate (and) PEG 100 Stearate does not substantially thicken emulsions, even in emulsions with very large oil phases. It is also substantially more stable in very thin emulsions. For example, let’s imagine we have four different emulsions; 2 emulsified with Polawax, and 2 emulsified with Glyceryl Stearate (and) PEG 100 Stearate. One of each emulsifier has a 15% oil phase, and the other two have a 30% oil phase—the only ingredients in the oil phase are a liquid oil and the emulsifier. There are no added thickeners, like gums or fatty alcohols (cetyl alcohol, cetearyl alcohol, etc.) The Polawax emulsions will have drastically different viscosities. The 15% one will be fairly thin, but still lotion-y. It would work well in a pump-top bottle, or possibly even a bottle with a treatment pump cap. The 30% one will be more like a cream; thick and rich, and much better suited to a jar or tub. The Glyceryl Stearate (and) PEG 100 Stearate emulsions will have very similar viscosities. The 15% one will be about the consistency of partly skimmed milk, while the 30% one will be more like cream. The 30% one is more viscous because the inner phase (the oil phase) is larger, but that viscosity difference is pretty small—especially when compared to differing phase sizes in an emulsion made with Polawax. Both Glyceryl Stearate (and) PEG 100 Stearate emulsions could be packaged in a spray bottle, and are far too thin for any sort of pump bottle or jar. Because Glyceryl Stearate (and) PEG 100 Stearate does not thicken emulsions, it gives us the ability to control the viscosity and oil phase size independently. For instance, you can create an emulsion with a 50% oil phase and decide if you want it to be a thinner, pumpable lotion or a thick, solid cream. You can also choose what you want to thicken it with, allowing you significantly more control over the skin feel of the finished product. With an emulsifying wax like Polawax, that product could only be solid, and the skin feel will be harder to adjust given the unavoidable presence of the thickeners in Polawax. Additionally, because Glyceryl Stearate (and) PEG 100 Stearate doesn’t add viscosity to our emulsions, it has the ability to create far lighter feeling emulsions—in that way, it’s almost ‘invisible’ in your formulations. If you want to add the fluffy creaminess and weight of cetearyl alcohol, you’ll have to add it yourself—if you used Emulsifying Wax NF instead, that already contains 65–80% cetearyl alcohol, so you can’t avoid it. Glyceryl Stearate (and) PEG 100 Stearate also works at lower rates than more common emulsifying waxes. Compared to Emulsifying Wax NF, Glyceryl Stearate (and) PEG 100 Stearate contains a higher percentage of the emulsifying ingredient. Emulsifying Wax NF contains 20–35% Polysorbate 60, while Glyceryl Stearate (and) PEG 100 Stearate contains approximately 50% PEG 100 Stearate. I’ve seen (and successfully used) Glyceryl Stearate (and) PEG 100 Stearate at 9–17% of the oil phase, compared to 20–25% for emulsifying waxes like Polawax, Emulsifying Wax NF, Olivem 1000, and Ritamulse SCG. Do you need it? I highly recommend it if you love making lotions—it gives you far more control over your emulsions than emulsifying waxes like Polawax and Ritamulse SCG. Refined or unrefined? Glyceryl Stearate (and) PEG 100 Stearate only exists as a refined product. Strengths It’s extremely versatile, allowing you to independently adjust the viscosity and oil phase size of your formulations. It easily creates stable emulsions at low usage rates and works brilliantly over a wide variety of oil phase sizes. It’s lightweight, inexpensive, and very effective. Weaknesses It isn’t considered natural; that doesn’t bother me as it is a perfectly safe ingredient, but I can’t offer a suitable naturally-accepted alternative at this time. Alternatives & Substitutions Glyceryl Stearate (and) PEG 100 Stearate is a tricky ingredient to substitute out. Generally speaking, you’ll need another complete emulsifying wax (something like Emulsifying Wax NF or Olivem 1000), but those complete emulsifying waxes contribute significantly more thickening to finished products, meaning formulations designed to work with Glyceryl Stearate (and) PEG 100 Stearate will likely be significantly more viscous if you use a thickening emulsifying wax in its place. Depending on the formulation you may be able to adequately compensate by removing any additional fatty thickeners, but this will take some experimenting to get right. If the formulation is for an ultra-light body milk or a very thick emulsified body butter type project, it will be difficult to substitute the emulsifier. You will likely be in re-formulation territory, or you will need to accept a more viscous and/or waxier/heavier end product. How to Work with It Include Glyceryl Stearate (and) PEG 100 Stearate in your heated oil phase. Storage & Shelf Life Stored somewhere cool, dark, and dry, Glyceryl Stearate (and) PEG 100 Stearate should last at least two years. Tips, Tricks, and Quirks Glyceryl Stearate (and) PEG 100 Stearate is different from Glyceryl Stearate SE, though both are emulsifiers. The Body Shop uses Glyceryl Stearate (and) PEG 100 Stearate to emulsify their signature body butters! Polyethylene Glycol (PEG) Stearates (PEG-2 Stearate, PEG-6 Stearate, PEG-8 Stearate, PEG-12 Stearate, PEG-20 Stearate, PEG-32 Stearate, PEG-40 Stearate, PEG-50 Stearate, PEG-100 Stearate, PEG-150 Stearate) are esters of polyethylene glycol and stearic acid. The PEG Stearates are soft to waxy solids that are white to tan in color. In cosmetics and personal care products, PEG Stearates are used in skin creams, conditioners, shampoos, body cleansers and soapless detergents. PEG 100 Stearate is used in cosmetics and beauty products primarily as a surfactant and cleansing agent, because PEG Stearates' ability to clean the skin and hair by helping water to mix with oil and dirt so that they can be rinsed away, according to. However, it is also seen as an emollient, because of secondary properties. * A surfactant and cleansing agent * Please read TIA’s article on What Is PEG 100 Stearate : PEGs Functions of PEG 100 Stearate : PEG 100 Stearate is used in cosmetics and beauty products primarily as a surfactant and cleansing agent, because PEG Stearates' ability to clean the skin and hair by helping water to mix with oil and dirt so that they can be rinsed away, according to CosmeticsInfo.org. However, it is also seen as an emollient, because of secondary properties. Unlike typical PEGs, (whose identifying number corresponds to their molecular weight) the numerical value of each PEG Stearate corresponds to the average number of ethylene oxide monomers in the polyethylene chain (from 2 - 150). Despite the many fears regarding PEGs, they are seen as an ingredient in a large number of products because of their diverse properties. In a study published in the Toxicology journal in 2005, entitled "Safety assessment on polyethylene glycols (PEGs) and their derivatives as used in cosmetic products," it was concluded that: "Taking into consideration all available information from related compounds, as well as the mode and mechanism of action, no safety concern with regard to these endpoints could be identified. Based on the available data it is therefore concluded that PEGs of a wide molecular weight range (200 to over 10,000), their ethers (laureths. ceteths, ceteareths, steareths, and oleths), and fatty acid esters (laurates, dilaurates, stearates, distearates) are safe for use in cosmetics." PEG 100 Stearate is not considered to be an irritant or sensitizer (it gave only minimal irritation in studies up to 100%), and are CIR and FDA approved for use, but not on broken skin (Source). Safety Measures/Side Effects of PEG 100 Stearate: However. The Cosmetics Database found PEG 40 Stearate to be a moderate to high hazard ingredient depending on usage. The EWG issues warnings regarding: cancer, developmental and reproductive toxicity, contamination concerns, irritation, and organ system toxicity. According to a study published in the International Journal of Toxicology, PEGs (including PEG 40 Stearate) can contain harmful impurities, including: Ethylene Oxide, known to increase the incidences of uterine and breast cancers and of leukemia and brain cancer, according to experimental results reported by the National Toxicology Program; 1,4-dioxane, a known carcinogen; PAHs, known to increase the risk of breast cancer; lead; iron; and arsenic (Source). Products and formulas containing PEG 40 Stearate should not be used on broken or irritated skin. Although PEGs are considered safe for use topically on healthy skin, studies showed that patients suffering from severe burns were treated with PEG-based antimicrobial cream; this treatment resulted in kidney toxicity. "The PEG content of the antimicrobial cream was determined to be the causative agent. However, no evidence of systemic toxicity occurred in studies with intact skin. Because of the observation of kidney effects in burn patients, the CIR Expert Panel qualified their conclusion on the safety of the PEG ingredients to state that cosmetic formulations containing these ingredients should not be used on damaged skin" SYNONYMS of PEG 100 Stearate Polyoxyl (40) stearate, polyoxyethylene (40) monostearate; INS No. 431 DEFINITION Consists of a mixture of the mono- and diesters of edible commercial stearic acid and mixed polyoxyethylene diols (having an average polymer length of about 40 oxyethylene units) together with free polyol. Structural formula Nominal formula and approximate composition: free polyol monoester diester where RCO- is a fatty acid moiety, and "n" has an average value of approximately 40. The distribution of polymers is approximately in accordance with the Poisson expression. Assay Not less than 84.0 and not more than 88.0% of oxyethylene groups equivalent to not less than 97.5 and not more than 102.5% of polyoxyethylene (40) stearate calculated on the anhydrous basis. DESCRIPTION of PEG 100 Stearate Cream-coloured and exists as flakes or as a waxy solid at 25o with a faint odour FUNCTIONAL USESEmulsifier of PEG 100 Stearate CHARACTERISTICS of PEG 100 Stearate IDENTIFICATION of PEG 100 Stearate Solubility (Vol. 4) Soluble in water, ethanol, methanol and ethylacetate; insoluble in mineral oil Congealing range (Vol. 4)39 - 44o Infrared absorption The infrared spectrum of the sample is characteristic of a partial fatty acid ester of a polyoxyethylated polyol Colour reaction To 5 ml of a 5% (w/v) aqueous solution of the sample add 10 ml of ammonium cobaltothiocyanate solution and 5 ml of chloroform, shake well and allow to separate; a blue colour is produced in the chloroform layer. (Ammonium cobaltothiocyanate solution: 37.5 g of cobalt nitrate and 150 g of ammonium thiocyanate made up to 100 ml with water - freshly prepared). Saponification (Vol. 4) 100 g of the sample yields approximately 13-14 g of fatty acids and 85-87 g of polyols PURITY of PEG 100 Stearate Water (Vol. 4) Not more than 3% (Karl Fischer Method) Acid value (Vol. 4) Not more than 1 Saponification value (Vol. 4) Not less than 25 and not more than 35 Hydroxyl value (Vol. 4) Not less than 27 and not more than 40 Lead (Vol. 4) Not more than 2 mg/kg Determine using an atomic absorption technique appropriate to the specified level. The selection of sample size and method of sample preparation may be based on the principles of the method described in Volume 4, “Instrumental Methods.” METHOD OF ASSAY of PEG 100 Stearate Determine the content of Oxyethylene groups. Polyoxyethylene (100) stearate has been used in a study to assess the phase behaviors of special hot microemulsion to produce drug-loaded nanostructured lipid carriers. [3] It has also been used in a study to investigate its effects on multidrug resistance (MDR). Polyoxyethylene 100 monostearate, also known as ethylene glycol monostearate or myrj 52, belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. Polyoxyethylene 40 monostearate is considered to be a practically insoluble (in water) and relatively neutral molecule. Polyoxyethylene 40 monostearate has been primarily detected in urine. Within the cell, polyoxyethylene 40 monostearate is primarily located in the membrane (predicted from logP) and cytoplasm. A sample work-up method for gas chromatographic profiling of polyethylene glycol related cmpd in pharmaceutical matrixes is described. After a short sample clean-up, carbon-oxygen linkages were partially cleaved with 0.07/M BBr3 in CH2Cl2 at room temp. The reaction was stopped after 1 min by addn of 0.01M hydrochloric acid. The products were trimethylsilylated and injected onto a WCOT 50 m X 0.25 mm CP-SIL 5 CB fused silica column. Eleven model cmpd, representing 4 common types of polyethylene glycol deriv, were evaluated by this method. Characteristic profiles can be obtained from polyethylene glycol deriv carrying different functional groups. Minimum detectable amt are in the range of 200 ug. Polyoxyl 100 Stearate is used in cosmetics and beauty products primarily as a surfactant and emulsifier. It occurs naturally as a white, waxy or flaky substance, according to The Food and Agriculture Organization of the United Nations. CosmeticsInfo.org notes that Polyoxyl 40 Stearate, as part of the PEG Stearate group, are formed from a naturally fatty acid known as Stearic Acid. The PEG Sterates are used in cosmetics and skin care formulas because they can "clean the skin and hair by helping water to mix with oil and dirt so that they can be rinsed away. Polyethylene glycol (PEG 100 Stearate ; /ˌpɒliˈɛθəlˌiːn ˈɡlaɪˌkɒl, -ˌkɔːl/) is a polyether compound with many applications, from industrial manufacturing to medicine. PEG 100 Stearate is also known as polyethylene oxide (PEO) or polyoxyethylene (POE), depending on its molecular weight. The structure of PEG 100 Stearate is commonly expressed as H−(O−CH2−CH2)n−OH.[3] Uses of PEG 100 Stearate Medical uses of PEG 100 Stearate PEG 100 Stearate is the basis of a number of laxatives.[4] Whole bowel irrigation with polyethylene glycol and added electrolytes is used for bowel preparation before surgery or colonoscopy. PEG 100 Stearate is also used as an excipient in many pharmaceutical products. When attached to various protein medications, polyethylene glycol allows a slowed clearance of the carried protein from the blood.[5] The possibility that PEG 100 Stearate could be used to fuse axons is being explored by researchers studying peripheral nerve and spinal cord injury.[4] Chemical uses of PEG 100 Stearate The remains of the 16th century carrack Mary Rose undergoing conservation treatment with PEG 100 Stearate in the 1980s Terra cotta warrior, showing traces of original color Because PEG 100 Stearate is a hydrophilic molecule, it has been used to passivate microscope glass slides for avoiding non-specific sticking of proteins in single-molecule fluorescence studies.[6] Polyethylene glycol has a low toxicity and is used in a variety of products.[7] The polymer is used as a lubricating coating for various surfaces in aqueous and non-aqueous environments.[8] Since PEG 100 Stearate is a flexible, water-soluble polymer, it can be used to create very high osmotic pressures (on the order of tens of atmospheres). It also is unlikely to have specific interactions with biological chemicals. These properties make PEG 100 Stearate one of the most useful molecules for applying osmotic pressure in biochemistry and biomembranes experiments, in particular when using the osmotic stress technique. Polyethylene glycol is also commonly used as a polar stationary phase for gas chromatography, as well as a heat transfer fluid in electronic testers. PEG 100 Stearate has also been used to preserve objects that have been salvaged from underwater, as was the case with the warship Vasa in Stockholm,[9] and similar cases. It replaces water in wooden objects, making the wood dimensionally stable and preventing warping or shrinking of the wood when it dries.[4] In addition, PEG 100 Stearate is used when working with green wood as a stabilizer, and to prevent shrinkage.[10] PEG 100 Stearate has been used to preserve the painted colors on Terracotta Warriors unearthed at a UNESCO World Heritage site in China.[11] These painted artifacts were created during the Qin Shi Huang (first emperor of China) era. Within 15 seconds of the terra-cotta pieces being unearthed during excavations, the lacquer beneath the paint begins to curl after being exposed to the dry Xi'an air. The paint would subsequently flake off in about four minutes. The German Bavarian State Conservation Office developed a PEG 100 Stearate preservative that when immediately applied to unearthed artifacts has aided in preserving the colors painted on the pieces of clay soldiers.[12] PEG 100 Stearate is often used (as an internal calibration compound) in mass spectrometry experiments, with its characteristic fragmentation pattern allowing accurate and reproducible tuning. PEG 100 Stearate derivatives, such as narrow range ethoxylates, are used as surfactants. PEG 100 Stearate has been used as the hydrophilic block of amphiphilic block copolymers
PEG 120 METHYL GLUCOSE DIOLEATE
PEG 120 METHYL GLUCOSE DIOLEATE (Peg 120 Methyl Glucose Dioleate) A surfactant and emulsifier PEG 120 Methyl Glucose Dioleate is the polyethylene glycol ether of the diester of natural Methylglucose and Oleic Acid. It is used in beauty products and cosmetics as a surfactant and emulsifier. It is used as a thickener in hair and skin care products. It is considered a non-irritant, and also has a specific property that allows it to reduce the irritation value of whole formulas (Source). The high molecular weight of this specific PEG makes it impenetratable to healthy skin; it is FDA and CIR approved for use, but not on broken skin Functions: PEG 120 Methyl Glucose Dioleate is the polyethylene glycol ether of the diester of natural Methylglucose and Oleic Acid. It is used in beauty products and cosmetics as a surfactant and emulsifier. It is used as a thickener in hair and skin care products. It is considered a non-irritant, and also has a specific property that allows it to reduce the irritation value of whole formulas (Source). The high molecular weight of this specific PEG makes it impenetratable to healthy skin; it is FDA and CIR approved for use, but not on broken skin. Despite the many fears regarding PEGs (including PEG 120 Methyl Glucose Dioleate), they are seen as an ingredient in a large number of products because of their diverse properties. In a study published in the Toxicology journal in 2005, entitled "Safety assessment on polyethylene glycols (PEGs) and their derivatives as used in cosmetic products," it was concluded that: "Taking into consideration all available information from related compounds, as well as the mode and mechanism of action, no safety concern with regard to these endpoints could be identified. Based on the available data it is therefore concluded that PEGs of a wide molecular weight range (200 to over 10,000), their ethers (laureths, ceteths, ceteareths, steareths, and oleths), and fatty acid esters (laurates, dilaurates, stearates, distearates) are safe for use in cosmetics." Safety Measures/Side Effects PEG 120 Methyl Glucose Dioleate: Benefits: •Very effective non-ionic, liquid thickener for various surfactant and emulsion systems •Due to its liquid form it is easily incorporated into a wide range of products •Excellent in cold processed formulations •Can be used for clear surfactant systems •Does not need to be neutralized with an alkali •Recommended for mild cleansing systems to reduce irritancy of surfactants Use: Use levels 0.5-3% depending on application and amount of thickening required. Note: at colder temperatures Glucose-D can solidify and become thick like a gel. For easier handling we recommend to put the bottle first into a water bath (about 50-60oC) for 10min. For external use only. Applications: Body washes, shampoos, face cleansers. Country of Origin: USA Raw material source: Rapeseed oil, ethylene oxide Manufacture: Peg 120 Methyl Glucose Dioleate and methyl gluceth-10 are produced from fatty acids and then reacted with ethylene oxide. Peg 120 Methyl Glucose Dioleate is derived from corn, it is a thickening agent for mild cleansing systems, it also reduces the irritancy of surfactant packages. It is the polyethylene glycol ether of the diester of natural Methyl glucose and Oleic Acid. It is used in beauty products and cosmetics as a surfactant and emulsifier. It is used as a thickener in hair and skin care products. GlucamateTM DOE-120 thickener is an ethoxylated methyl glucose ether which has been esterified with oleic acid. It is an extremely effective nonionic thickener for hair care and skin care products. This product is recommended for use in shower gels, facial cleansers and shampoos. TYPICAL PRODUCT SPECIFICATIONS NOTES : Peg 120 Methyl Glucose Dioleate is a PEG ether of the diester of methyl glucose and oleic acid with avg. 120 moles of ethylene oxide Peg 120 Methyl Glucose Dioleate uses and applications include: Thickener, emulsifier, solubilizer for shampoos, cosmetics, topical pharmaceuticals; anti-irritant for surfactants CLASS : Surfactants FUNCTIONS : Surfactant, Emulsifier, Acid INDUSTRY : Cosmetic, Pharmaceutical APPEARANCE Pale yellow flake Yellow-brown viscous liquid FUNCTION : Peg 120 Methyl Glucose Dioleate is an extremely effective nonionic thickener for hair care and skin care products. STORAGE : Store in a cool dry place. Store only with compatible chemicals. Keep tightly closed. USE: It is a kind of high-efficient thickener in shampoo, body wash, facial cleanser and baby cleanser Physical and Chemical Properties Polypropylene glycol-20 methyl glucose ether acetate is soluble in oils and organic solvents, but is essentially insoluble in water.2 A log Kow of 13.98 has been reported for d-glucopyranoside, methyl, 2,6-di-9-octadecenoate, (Z,Z)-(Chemical Abstracts Service Number 82933-91-3), another name for methyl glucose dioleate.3 A log Kow ≈ 7.09 has been reported for methyl glucose sesquistearate.4 Specifications for methyl glucoside-coconut oil ester (methyl glucose sesquicocoate) as a direct food additive are as follows5: acid number (10-20), hydroxyl number (200-300), pH (4.8-5.0, for 5% aqueous), and saponification number (178-190). Physical and chemical properties associated with methyl glucose polyether and ester trade name materials are included in Tables 3, 4, and 5.6 Studies on most of these trade name materials are included in the toxicology section of this article. Additionally, the chemical and physical properties of isostearic acid (esters with methyl α-d-glucoside [registered with the European Chemicals Industry, ECHA], defined as 80% methyl glucoside isostearate esters [mainly di-], 16% isostearic acid, and 4% methyl glucoside)7 are included in Table 6. Data on this mixture are also included in the toxicology section. Method of Manufacture Methyl glucoside (methyl α-d-glucopyranoside) forms the backbone of the methyl glucose polyethers and esters reviewed in this safety assessment. It is cyclic or "internal" full acetal that is formed from 1 mole of methanol and 1 mole of glucose. It has been characterized as an unusually stable glucoside that exists in discrete α or β forms.16 The pathways for methyl glucoside ester and polyether methyl glucoside synthesis starting from methyl glucoside are diagrammed in Figure 1.Manufacture of methyl glucoside esters, such as methyl glucose caprylate/caprate, methyl glucose dioleate, methyl glucose isostearate, methyl glucose laurate, methyl glucose sesquicaprylate/sesquicaprate, methyl glucose sesquicocoate, methyl glucose sesquiisostearate, methyl glucose sesquilaurate, methyl glucose sesquioleate, and methyl glucose sesquistearate, is typically achieved via transesterification of an appropriate fatty acid methyl ester (eg, methyl laurate to get methyl glucose laurate) with methyl glucoside (releasing methanol as a by-product).8-13 However, esterifications via a variety of other classical techniques, such as reacting the free fatty acids with methyl glucoside and a catalyst, are also known methods of manufacture for these ingredients.14,15 Under most conditions, the primary alcohol group at C6 of the methyl glucoside core is the most reactive to esterification and is the first site to be substituted. The polyether methyl glucosides, such as PPG-10 methyl glucose ether, PPG-20 methyl glucose ether, PPG-25 methyl glucose ether, methyl gluceth-10, and methyl gluceth-20, are typically manufactured by reaction of methyl glucoside with the required amount of the appropriate epoxide (eg, propylene oxide is used to produce PPG-10 methyl glucose; ethylene oxide is utilized to produce methyl gluceth-10).10 For those ingredients with both ester and polyether groups, such as Peg 120 Methyl Glucose Dioleate, PEG-20 methyl glucose distearate, PEG-80 methyl glucose laurate, PEG-20 methyl glucose sesquicaprylate/sesquicaprate, PEG-20 methyl glucose sesquilaurate, PEG-20 methyl glucose sesquistearate, PEG-120 methyl glucose triisostearate, PEG-120 methyl glucose trioleate, PPG-20 methyl glucose ether acetate, and PPG-20 methyl glucose ether distearate, these same methods are utilized, sequentially. An example would be PEG-80 methyl glucose laurate, which is produced in 2 steps: (1) esterification of methyl glucoside with methyl laurate, followed by (2) polyetherification with ethylene oxide. Use Cosmetic The methyl glucose polyethers reportedly function as skin and hair-conditioning agents, whereas, the methyl glucose esters reportedly function only as skin-conditioning agents in cosmetic products.1 Ingredients classified as both methyl glucose polyethers and esters based on their chemical structures function as skin-conditioning agents, surfactants, and viscosity-increasing agents in cosmetic products. According to the information supplied to the Food and Drug Administration (FDA) by industry as part of the Voluntary Cosmetic Registration Program (VCRP) in 2013 (summarized in Table 7), methyl glucose dioleate, methyl glucose sesquioleate, methyl glucose sesquistearate, PPG-10 methyl glucose ether, PPG-20 methyl glucose ether, PPG-20 methyl glucose ether distearate, methyl gluceth-10, methyl gluceth-20, Peg 120 Methyl Glucose Dioleate, PEG-20 methyl glucose distearate, PEG-20 methyl glucose sesquistearate, and PEG-120 methyl glucose trioleate are being used in cosmetic products.17 A survey of ingredient use concentrations that was conducted by the Personal Care Products Council (Council) in 2013 (Table 7) indicates that the polyethers and esters are being used at concentrations up to 15% and 4%, respectively.18,19 The maximum use concentration was 15% for methyl gluceth-10 and methyl gluceth-20 used in rinse-off skin-cleansing products. For leave-on products, the 15% maximum use concentration was for methyl gluceth-10 used in face and neck creams, lotions, and powders (not sprays). The Council survey results also provided a use concentration for the newly reported VCRP use(s) of methyl glucose sesquistearate (1% maximum use concentration), but not PEG-20 methyl glucose sesquistearate, in lipsticks. Additionally, a maximum use concentration of 0.05% for PEG-20 methyl glucose distearate in lipsticks was reported in this survey. Uses of methyl glucose sesquistearate and PEG-20 methyl glucose sesquistearate, but not PEG-20 methyl glucose distearate, in lipsticks were also reported in FDA's VCRP. Cosmetic products containing methyl glucose polyethers and esters may be applied to the skin and hair, or, incidentally, may come in contact with the eyes and mucous membranes. Products containing these ingredients may be applied as frequently as several times per day and may come in contact with the skin or hair for variable periods following application. Daily or occasional use may extend over many years. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is the polyethylene glycol ether of the diester of natural Methylglucose and Oleic Acid. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is used in beauty products and cosmetics as a surfactant and emulsifier. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is used as a thickener in hair and skin care products. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is considered a non-irritant, and also has a specific property that allows PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) to reduce the irritation value of whole formulas (Source). The high molecular weight of this specific PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) impenetratable to healthy skin; PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is FDA and CIR approved for use, but not on broken skin PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) thickener is an ethoxylated methyl glucose ether which has been esterified with oleic acid. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is an extremely effective nonionic thickener for hair care and skin care products. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is recommended for use in shower gels, facial cleansers and shampoos. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is a very popular skin care ingredient and are used to dissolve oil and grease. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is used in skin care products as thickeners and stabalizers, and to PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) help dissolve oil on skin. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is an extremely effective non-ionic thickener for hair care and skin care products, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) recommended in shower gels, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) recommended in facial cleansers and PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) recommended in shampoos. Actives: 70-80%. Remaining part: water. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is viscous liquid, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) light yellow color. An LD50 of > 5 g/kg was also reported for PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) in a study involving rats (number and strain not stated). PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) Details relating to the test protocol were not stated. The ocular irritation potential of PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) was evaluated in the Draize test using 5 male or female New Zealand albino rabbits.37 The test substance (100 µl) was instilled into one eye of each animal. Instillation was followed by massaging for 30 seconds. Untreated eyes served as controls. Reactions were scored at 24 h, 48 h, 72 h, and 7 days post-instillation PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) , and maximum average Draize scores (MAS; range: 0 to 110) were determined. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) was classified as a slight irritant (maximum average Draize score = 8.8). An in vitro assay was conducted to determine if there was a correlation with the in vivo Draize test conducted on rabbits. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) Using sheep red blood cells, this in vitro assay assessed hemolysis and protein denaturation. The extent of hemolysis was determined spectrophotometrically. Assay results for PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) were as follows: effective concentration that caused 50% hemolysis (H50) = 1,125.56 µg/ml; denaturation index (DI) = 12.82%; H50/DI = 87.80. The Pearson and Spearman PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) correlation coefficients between the log H50/DI and the MAS were 0.752 and 0.705, respectively. Thus, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) was also classified as a slight irritant in the in vitro assay. The ocular irritation potential of 100% PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) was evaluated in the Draize test using rabbits (number and strain not stated).32 The test substance did not induce ocular irritation. In comparative irritation tests, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) (concentrations not stated) significantly reduced the ocular irritation induced by SLS and AOS in rabbits (number and strain not stated). The PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) abbreviated chemical names were not defined. The skin irritation potential of 100% The PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) (GlucamTM DOE-120 Thickener) was evaluated using rabbits (number and strain not stated).32 Details relating to the test protocol were not included. A primary irritation The PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) index of 0.45 (range: 0 to 8) was reported. % PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) was evaluated in an HRIPT (occlusive patches) involving 53 atopic volunteers. n the Ames plate incorporation test, the genotoxicity of PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) (in ethanol) was evaluated at doses up to 5000 µg/plate. It was concluded that PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) was not genotoxic in any of the bacterial strains tested, with or without metabolic activation. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is derived from corn, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is a thickening agent for mild cleansing systems, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) also reduces the irritancy of surfactant packages. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is the polyethylene glycol ether of the diester of natural Methyl glucose and Oleic Acid. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is used in beauty products and cosmetics as a surfactant and emulsifier. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is used as a thickener in hair and skin care products. Ingredients: PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) : PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is a naturally derived cleansing and thickening agent for shampoos and other cleansing products. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) also has good moisture retention properties which can help PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) improve the skin-feel of surfactant-based products. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is derived from corn and palm and then ethoxylated to make PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) wate soluble. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is usually a petrochemical process. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) Soluble in hot water. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) comes as flakes that will soften and dissolve into a water base but PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) can be quite slow at room temperature. The best procedure is to heat a little of your water to 50-60C and add the PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) , forming a fluid paste which can then be added into the rest of your formula for thickening. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) uses as a thickening and cleansing agent for shampoos and cleansing products. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is Polyethylene glycol ether of the diester of methyl glucose and oleic acid with an average of 120 moles of ethylene oxide. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) Surfactant/thickener/solubilizer/emulsifier mainly used in cosmetics and personal care products. For those ingredients with both ester and polyether groups, such as PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) , PEG-20 methyl glucose distearate, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) , PEG-20 methyl glucose sesquicaprylate/sesquicaprate, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) PEG-20 methyl glucose sesquistearate, PEG-120 methyl glucose triisostearate, PEG-120 methyl glucose trioleate, PPG-20 methyl glucose ether acetate, and PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) these same methods are utilized, sequentially. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is a PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) ether of the diester of methyl glucose and oleic acid with avg. 120 moles of ethylene oxide PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) uses and applications include: PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is used as Thickener, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is used as emulsifier, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is used as solubilizer for shampoos, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is used in cosmetics, topical pharmaceuticals; anti-irritant for surfactants. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is commonly included in medications in the following forms. Cas no of PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is 86893-19-8. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) ; DOE 120 is an extremely effective nonionic thickener for hair care and skin care products, derives from natural methyl glucoside. And it has non-irritation for eyes, which ideally is applied for baby shampoos and face wash products. It is a good ingredient for low irritation formulation, based on its specific property梔istinctly reduce the irritation of whole formulation. Appearance of PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) Pale yellow flake liquid Odor of PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) Mild characteristic Acid value, mg/g of PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) 1MAX Hydroxyl value, mg/g of PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) 14-26 Saponification value, mg/g of PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) 14-26 Iodine value of PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) 5-15 pH,(5% aqueous solution) of PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) 4.5-8.0 PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) : PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is a polyethylene glycol ether of the diester of methylglucose and oleic acid with an average of 120 moles of ethylene oxide. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is used in skin care and hair care products as a surfactant and emulsifier. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is considered a non-irritant, and also has a specific property that allows PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) to reduce the irritation value of whole formulas. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is known to be a moderate hazard depending on use and warns of contamination and toxicity concerns. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) including products should not be used on broken or irritated skin as studies showed that patients suffering from severe burns treated with PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) based antimicrobial cream has resulted in kidney toxicity. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is also known to increase the incidences of uterine and breast cancers and of leukemia and brain cancer according to a study published in the PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) International Journal of Toxicology. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is FDA and CIR approved for use, but not on broken skin. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is a naturally derived cleansing and thickening agent for shampoos and other cleansing products. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) also has good moisture retention properties which can help PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) improve the skin-feel of surfactant-based products. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is a very popular skin care ingredient and are used to dissolve oil and grease. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is used in skin care products as thickeners and stabalizers, and to PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) help dissolve oil on skin. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is an extremely effective non-ionic thickener for hair care and skin care products, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) recommended in shower gels, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) recommended in facial cleansers and PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) recommended in shampoos. Actives: 70-80%. Remaining part: water. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is viscous liquid, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) light yellow color. An LD50 of > 5 g/kg was also reported for PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) in a study involving rats (number and strain not stated). PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) Details relating to the test protocol were not stated. The ocular irritation potential of PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) was evaluated in the Draize test using 5 male or female New Zealand albino rabbits.37 The test substance (100 µl) was instilled into one eye of each animal. Instillation was followed by massaging for 30 seconds. Untreated eyes served as controls. Reactions were scored at 24 h, 48 h, 72 h, and 7 days post-instillation PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) , and maximum average Draize scores (MAS; range: 0 to 110) were determined. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) was classified as a slight irritant (maximum average Draize score = 8.8). An in vitro assay was conducted to determine if there was a correlation with the in vivo Draize test conducted on rabbits. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) Using sheep red blood cells, this in vitro assay assessed hemolysis and protein denaturation. The extent of hemolysis was determined spectrophotometrically. Assay results for PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) were as follows: effective concentration that caused 50% hemolysis (H50) = 1,125.56 µg/ml; denaturation index (DI) = 12.82%; H50/DI = 87.80. The Pearson and Spearman PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) correlation coefficients between the log H50/DI and the MAS were 0.752 and 0.705, respectively. Thus, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) was also classified as a slight irritant in the in vitro assay. The ocular irritation potential of 100% PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) was evaluated in the Draize test using rabbits (number and strain not stated).32 The test substance did not induce ocular irritation. In comparative irritation tests, PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) (concentrations not stated) significantly reduced the ocular irritation induced by SLS and AOS in rabbits (number and strain not stated). The PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) abbreviated chemical names were not defined. The skin irritation potential of 100% The PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) (GlucamTM DOE-120 Thickener) was evaluated using rabbits (number and strain not stated).32 Details relating to the test protocol were not included. A primary irritation The PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) index of 0.45 (range: 0 to 8) was reported. % PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) was evaluated in an HRIPT (occlusive patches) involving 53 atopic volunteers. n the Ames plate incorporation test, the genotoxicity of PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) (in ethanol) was evaluated at doses up to 5000 µg/plate. It was concluded that PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) was not genotoxic in any of the bacterial strains tested, with or without metabolic activation. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is the polyethylene glycol ether of the diester of natural Methyl glucose and Oleic Acid. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is used in beauty products and cosmetics as a surfactant and emulsifier. PEG 120 Methyl Glucose Dioleate (PEG-120 Methyl Glucose Dioleate, PEG 120 METHYL GLUCOSE DIOLEATE) is used as a thickener in hair and skin care products. PEG 120 Methyl Glucose Dioleate (P
PEG 120 METHYL GLUCOSE DIOLEATE
PEG 120 Methyl Glucose Dioleate is feeling quite soft and gentle after applying.
PEG 120 Methyl Glucose Dioleate has a slight emulsifying ability.
PEG 120 Methyl Glucose Dioleate is pale yellow flake,with mild characteristic odor.


CAS Number: 86893-19-8
EC Number: 617-932-4
Chem/IUPAC Name: Poly(oxy-1,2-ethanediyl), .alpha.-hydro-.omega.-hydroxy-, ether with methyl d-glucopyranoside 2,6-bis[(z)-9-octadecenoate]
Molecular Formula: C45H81O10
Molecular Formula: (C2H4O)mult(C2H4O)multC43H78O



SYNONYMS:
Antil 120 Plus, Unitol 120 Plus, PEG-120 Methyl Glucose Dioleate, Poly(oxy-1,2-ethanediyl),a-hydro-w-hydroxy-, ether with methylD-glucopyranoside 2,6-di-9-octadecenoate (2:1), (Z,Z)-, Poly(oxy-1,2-ethanediyl), α-hydro-ω-hydroxy-, ether with methyl D-glucopyranoside 2,6-di-(9Z)-9-octadecenoate (2:1), Poly(oxy-1,2-ethanediyl), α-hydro-ω-hydroxy-, ether with methyl D-glucopyranoside 2,6-di-9-octadecenoate (2:1), (Z,Z)-, PEG-120 methyl glucose dioleate, AEC PEG-120 METHYL GLUCOSE DIOLEATE, ANTIL 120 PLUS, GLUCAMATE DOE-120 THICKENER, MACROGOL 120 METHYL GLUCOSE DIOLEATE, PEG 120 methyl glucose dioleate, PEG-120 METHYL GLUCOSE DIOLEATE (II), POLYETHYLENE GLYCOL (120) METHYL GLUCOSE DIOLEATE, YM0K64F20V, AEC PEG-120 METHYL GLUCOSE DIOLEATE, ANTIL 120 PLUS, GLUCAMATE DOE-120 THICKENER, MACROGOL 120 METHYL GLUCOSE DIOLEATE, PEG-120 METHYL GLUCOSE DIOLEATE, PEG-120 METHYL GLUCOSE DIOLEATE [II], PEG-120 METHYL GLUCOSE DIOLEATE [VANDF], POLYETHYLENE GLYCOL (120) METHYL GLUCOSE DIOLEATE, Glucamate DOE 120, Antil 120, PEG 120 methyl glucose dioleate, Antil 120 Plus, Antil 127, Novethix HC 220, Novethix HC 220S, D-Glucopyranoside, methyl, 2,6-di-(9Z)-9-octadecenoate;D-Glucopyranoside, methyl, 2,6-di-9-octadecenoate, (Z,Z)-;D-Glucopyranoside methyl 2,6-dioleate, Poly(oxy-1,2-ethanediyl), alpha-hydro-omega-hydroxy-, ether with methyl D-glucopyranoside 2,6-di-9-octadecenoate (2:1), (Z,Z)-, Poly(oxy-1,2-ethanediyl), alpha-hydro-omega-hydroxy-, ether with methyl D-glucopyranoside 2,6-di-(9Z)-9-octadecenoate (2:1), Diethoxylated methyl glucopyranoside 2,6-dioleate, PEG-120 methyl glucose dioleate, Macrogol 120 methyl glucose dioleate, POE (120) methyl glucose dioleate



PEG 120 Methyl Glucose Dioleate is a natural glucose derivative from corn with the following properties.
PEG 120 Methyl Glucose Dioleate has the ability to thicken when combined with many anionic and amphoteric surfactants, creating transparent gels.
PEG 120 Methyl Glucose Dioleate is non-irritating to eyes, can be used in baby cleansers and shampoos.


PEG 120 Methyl Glucose Dioleate does not affect the foaming ability of the system
PEG 120 Methyl Glucose Dioleate is feeling quite soft and gentle after applying.
PEG 120 Methyl Glucose Dioleate has a slight emulsifying ability


PEG 120 Methyl Glucose Dioleate is very effective water retention properties that help prevent water loss from the skin
PEG 120 Methyl Glucose Dioleate is easy to introduce into products including cold process, no need to heat and no need to adjust the pH again.
PEG 120 Methyl Glucose Dioleate is a naturally-derived, methyl glucose ether which has been esterified with oleic acid.


PEG 120 Methyl Glucose Dioleate is a flaked solid, highly efficient viscosity builder designed for use with numerous anionic surfactants and amphoteric surfactant systems popular in many shampoos, body washes, and liquid soaps.
PEG 120 Methyl Glucose Dioleate is a PEG ether of the diester of methyl glucose and oleic acid with average 120 moles of ethylene oxide.


PEG 120 Methyl Glucose Dioleate is pale yellow flake,with mild characteristic odor.
PEG 120 Methyl Glucose Dioleate is the polyethylene glycol ether of the diester of natural Methylglucose and Oleic Acid.
PEG 120 Methyl Glucose Dioleate is considered a non-irritant, and also has a specific property that allows it to reduce the irritation value of whole formulas.


PEG 120 Methyl Glucose Dioleate is a polyethylene glycol ether of natural methyl glucose and oleic acid diester.
PEG 120 Methyl Glucose Dioleate is a naturally derived cleansing and thickening agent.
PEG 120 Methyl Glucose Dioleate also has good moisture retention properties which can help it improve the skin-feel of surfactant-based products


PEG 120 Methyl Glucose Dioleate is the polyethylene glycol ether of the diester of oleic acid and methylglucose.
The 120 represents an average of 120 moles of ethylene oxide.
There is limited research on this ingredient, although PEG 120 Methyl Glucose Dioleate is considered safe to use in skincare products.


PEG 120 Methyl Glucose Dioleate is high-efficient thickener for rinse-off products, even for some surfactants which are hard to be thickening.
PEG 120 Methyl Glucose Dioleate is en effective nonionic thickener for hair care and skin care products.
PEG 120 Methyl Glucose Dioleate has excellent mildness, it is high effective thickening agent in surfactant system.


PEG 120 Methyl Glucose Dioleate can decrease the irritation brought by surfactants, it won’t decrease the height of the foam.
PEG 120 Methyl Glucose Dioleate is slightly soluble in water.
PEG 120 Methyl Glucose Dioleate is stable under strong acid, strong alkaline condition, it is easy to hydrolyze, easily be oxidized.


PEG 120 Methyl Glucose Dioleate is biodegradable.
PEG 120 Methyl Glucose Dioleate is naturally derived product.
Moreover, PEG 120 Methyl Glucose Dioleate in skin care has been shown to possess anti-aging properties, with the potential to reduce the appearance of fine lines and wrinkles.


PEG 120 Methyl Glucose Dioleate can help to strengthen the skin's barrier function, protecting it from environmental stressors and preventing premature signs of aging.
Whether you're seeking to address specific skin concerns or simply wanting to enhance the overall health and appearance of your complexion, incorporating

PEG 120 Methyl Glucose Dioleate into your skin care routine can be a game-changing decision.
Discover the transformative power of this remarkable ingredient, PEG 120 Methyl Glucose Dioleate, and unlock the secret to beautiful, youthful-looking skin.
PEG 120 Methyl Glucose Dioleate is a naturally derived cleansing and thickening agent for shampoos and other cleansing products.


PEG 120 Methyl Glucose Dioleate also has good moisture retention properties which can help it improve the skin-feel of surfactant-based products.
PEG 120 Methyl Glucose Dioleate is derived from corn and palm and then ethoxylated to make it water soluble.
Ethoxylation is usually a petrochemical process.


PEG 120 Methyl Glucose Dioleate is soluble in hot water.
PEG 120 Methyl Glucose Dioleate comes as flakes that will soften and dissolve into a water base but this can be quite slow at room temperature.
The best procedure is to heat a little of your water to 50-60C and add the PEG 120 Methyl Glucose Dioleate, forming a fluid paste which can then be added into the rest of your formula for thickening.



USES and APPLICATIONS of PEG 120 METHYL GLUCOSE DIOLEATE:
PEG 120 Methyl Glucose Dioleate is used in products: Shampoo, shower gel, facial cleanser and other cleaning products.
PEG 120 Methyl Glucose Dioleate is non-irritating to the eyes, making it ideal for baby shampoos.
Applications of PEG 120 Methyl Glucose Dioleate: Facial Cleansers, Hand Soap, Intimate Cleansers, and Mild Cleansers.


PEG 120 Methyl Glucose Dioleate can be used in shampoos and cleansing products
PEG 120 Methyl Glucose Dioleate is used to improve texture and stability of a product.
PEG 120 Methyl Glucose Dioleate is sugar based and helps thicken a product.


Once applied, PEG 120 Methyl Glucose Dioleate also creates a thin film to trap moisture in.
PEG 120 Methyl Glucose Dioleate helps keep your skin hydrated.
PEG 120 Methyl Glucose Dioleate is used Baby shampoo, cleanser, hand soap, mild shampoo, shower gel, makeup remover


PEG 120 Methyl Glucose Dioleate uses and applications include: Thickener, emulsifier, solubilizer for shampoos, cosmetics, topical pharmaceuticals; anti-irritant for surfactants.
PEG 120 Methyl Glucose Dioleate is used in beauty products and cosmetics as a surfactant and emulsifier.


PEG 120 Methyl Glucose Dioleate is used as a thickener in hair and skin care products.
PEG 120 Methyl Glucose Dioleate is used as a surfactant and emulsifier in beauty products and cosmetics.
PEG 120 Methyl Glucose Dioleate is used as a thickening agent in hair and skin care products.


PEG 120 Methyl Glucose Dioleate is considered non-irritating and also has specific properties that reduce the irritation value of the entire formula.
PEG 120 Methyl Glucose Dioleate is used specialized for shampoo, shower gel, cleanser, baby cleaning products of high efficiency thickener
PEG 120 Methyl Glucose Dioleate is used Facial products, Facial care.


PEG 120 Methyl Glucose Dioleate is an effective nonionic thickener for hair care and skin care products.
PEG 120 Methyl Glucose Dioleate is majorly be used as emulsifier, thickener, plasticizer etc.
PEG 120 Methyl Glucose Dioleate has very good compatibility, it won’t decrease the foam of the surfactant system, it has good compatibility and thickening function using together with AOS, SLES, Sulfosuccinate and ampho-surfactant.


PEG 120 Methyl Glucose Dioleate has no jelly feeling, it have superior cooperativity.
PEG 120 Methyl Glucose Dioleate has very mild irritation to eye, test result shows the irritation to eye is zero, so it is ideal and perfect raw material of infant shampoo.


Besides, PEG 120 Methyl Glucose Dioleate can remarkably decrease the irritation to eye of other surfactants.
Because of its thickening and irritation relieving function, PEG 120 Methyl Glucose Dioleate is suitable to be produce cleaning products.
The formula designer can adopt PEG 120 Methyl Glucose Dioleate to produce pourable product which can produce beautiful foams, and meanwhile you don’t worry the foam characteristics are changed.


PEG 120 Methyl Glucose Dioleate is widely used for producing infant shampoo, facial cleaning cream, hand washing liquid, mild shampoo, body washing liquid, make up remover etc.
PEG 120 Methyl Glucose Dioleate is a natural glucose derivative from corn, acting as high-efficient thickener in shampoo, body wash, facial cleanser and baby cleanser.


PEG 120 Methyl Glucose Dioleate is especially applicable to some surfactants hardly to thicken.
PEG 120 Methyl Glucose Dioleate causes no irritation to eyes, meanwhile significantly reduces irritation of whole formula.
PEG 120 Methyl Glucose Dioleate is the polyethylene glycol ether of the diester of natural Methylglucose and Oleic Acid.


PEG 120 Methyl Glucose Dioleate can reduce the irritation value of the entire formulation.
Its high molecular weight makes PEG 120 Methyl Glucose Dioleate impenetrable to healthy skin.
PEG 120 Methyl Glucose Dioleate is available as a flaky solid or a liquid.


PEG 120 Methyl Glucose Dioleate is a remarkable ingredient that is making waves in the world of skin care, offering a multitude of benefits that can transform the way you approach your daily routine.
This versatile compound, PEG 120 Methyl Glucose Dioleate, has the power to nourish, hydrate, and protect your skin, making it an essential addition to any well-rounded skin care regimen.


From its ability to deeply hydrate and lock in moisture to its potential in reducing the appearance of fine lines and wrinkles, PEG 120 Methyl Glucose Dioleate is poised to become a game-changer in your skin care journey.
Recommendations: Use PEG 120 Methyl Glucose Dioleate between 2 - 6% in formulations


PEG 120 Methyl Glucose Dioleate is used as a thickening and cleansing agent for shampoos and cleansing products.
One of the standout features of PEG 120 Methyl Glucose Dioleate in skin care is its exceptional moisturizing prowess.
PEG 120 Methyl Glucose Dioleate has the ability to penetrate deep into the skin, delivering long-lasting hydration and preventing the development of dryness and flakiness.


By maintaining optimal moisture levels, PEG 120 Methyl Glucose Dioleate can help to improve the overall smoothness and suppleness of your complexion, leaving your skin feeling radiant and rejuvenated.
PEG 120 Methyl Glucose Dioleate is used in cosmetics as a surfactant, thickener, and emulsifier.



PROPERTIES OF PEG 120 METHYL GLUCOSE DIOLEATE:
*Superior ability to thicken many anionic and amphoteric surfactants.
*No irritation to eye, applicable in facial cleanser and baby shampoo.
*No effect on foamability.
*Impart quite soft and gentle after-feeling.



CHARACTERISTICS OF PEG 120 METHYL GLUCOSE DIOLEATE:
Characteristics:
PEG 120 Methyl Glucose Dioleate has good properties of emulsifying, dispersing, solubilization etc.
PEG 120 Methyl Glucose Dioleate is compatible to skin, feel comfortable.



INDUSTRY OF PEG 120 METHYL GLUCOSE DIOLEATE:
*Cosmetic ,
*Pharmaceutical



FUNCTIONS OF PEG 120 METHYL GLUCOSE DIOLEATE:
*Surfactant ,
*Emulsifier ,
*Acid



CHARACTERISTICS OF PEG 120 METHYL GLUCOSE DIOLEATE:
PEG 120 Methyl Glucose Dioleate also provides the following characteristics to formulations:
*Nonionic surfactant based
*PEG 120 Methyl Glucose Dioleate reduces irritation associated with surfactants
*PEG 120 Methyl Glucose Dioleate does not reduce foam height
*Very light feel
*PEG 120 Methyl Glucose Dioleate provides gelling and moisture
*Especially suitable for children and hand washing products
*PEG 120 Methyl Glucose Dioleate is a kind of mild non-ionic thickening agent, it can reduce formula irritation.



BENEFITS OF PEG 120 METHYL GLUCOSE DIOLEATE:
*Soothing,
*anti-inflammatory,
*Moisturizing, hydrating,
*Blurring, soft focus, pore minimising



FEATURES AND BENEFITS OF PEG 120 METHYL GLUCOSE DIOLEATE:
*Broad compatibility with various surfactant systems
*PEG 120 Methyl Glucose Dioleate enables formulations that are easy to pour and have aesthetically-pleasing foaming properties without the worry of changing foam characteristics
*PEG 120 Methyl Glucose Dioleate enables very mild formulations and reduces irritation associated with certain surfactants for application around the eyes
*Highly efficient thickener of surfactant system formulations
*Naturally derived
*Very light feel



PEG 120 METHYL GLUCOSE DIOLEATE MARKET OVERVIEW:
The PEG-120 Methyl Glucose Dioleate Market size is expected to develop revenue and exponential market growth at a remarkable CAGR during the forecast period from 2023–2030.

The growth of the market can be attributed to the increasing demand for PEG 120 Methyl Glucose Dioleate owning to the Personal Care, Cosmetics Applications across the global level.

The report provides insights regarding the lucrative opportunities in the PEG 120 Methyl Glucose Dioleate Market at the country level.
The report also includes a precise cost, segments, trends, region, and commercial development of the major key players globally for the projected period.

The PEG 120 Methyl Glucose Dioleate Market report represents gathered information about a market within an industry or various industries.
The PEG 120 Methyl Glucose Dioleate Market report includes analysis in terms of both quantitative and qualitative data with a forecast period of the report extending from 2023 to 2030.



BENEFIT OF PEG 120 METHYL GLUCOSE DIOLEATE:
PEG 120 Methyl Glucose Dioleate is used as an emulsifier to help oil and water mix easily



PEG 120 METHYL GLUCOSE DIOLEATE INSTRUCTIONS:
1.Under mild heating and moderate stirring conditions, add PEG 120 Methyl Glucose Dioleate to the system until completely dissolved, and then add other materials.

2.Mix A with water at a ratio of 1: 5-10, heat to dissolve, and then add the dissolved surfactant.



PERFORMANCE OF PEG 120 METHYL GLUCOSE DIOLEATE:
1. PEG 120 Methyl Glucose Dioleate is very efficient, has a very good thickening effect on a variety of anionic surfactants and amphoteric surfactants.

2.PEG 120 Methyl Glucose Dioleate has no irritation to eyes and is very suitable for cleansing products and baby shampoos.
At the same time, PEG 120 Methyl Glucose Dioleate can significantly reduce the irritation of eyes by other surfactants.

3.PEG 120 Methyl Glucose Dioleate does not affect the foam characteristics of the surfactant.



PHYSICAL and CHEMICAL PROPERTIES of PEG 120 METHYL GLUCOSE DIOLEATE:
Boiling Point: >200°C
Solubility: Soluble in water
Appearance: Yellowish or white Flake
Odor:Mild, characteristic
Saponification value(mgKOH/g):14-26
Hydroxyl value(mgKOH/g):14-26
Acid value(mgKOH/g):≤1.0
pH (10%solution, 25℃):4.5-7.5
Iodine value (g/100g):5-15

Appearance: Yellowish to white slice (Slice form)
Pale yellow flake (Flake form)
Odor: Characteristic scent (Slice form)
Mild characteristic (Flake form)
PH value (10% Aqueous solution): 4.5-7.5 (Both forms)
Iodine value (g/100g): 5.0-15.0 (Both forms)
Saponification value (mg/g): 14.0-26.0 (Both forms)
Hydroxyl value (mg/g): 14.0-26.0 (Both forms)
Acid value (mgKOH/g): ≤1.0 (Slice form) / 1 max (Flake form)



FIRST AID MEASURES of PEG 120 METHYL GLUCOSE DIOLEATE:
-Description of first-aid measures:
*If inhaled:
If breathed in, move person into fresh air.
*In case of skin contact:
Wash off with soap and plenty of water.
*In case of eye contact:
Flush eyes with water as a precaution.
*If swallowed:
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of PEG 120 METHYL GLUCOSE DIOLEATE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Keep in suitable, closed containers for disposal.



FIRE FIGHTING MEASURES of PEG 120 METHYL GLUCOSE DIOLEATE:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available



EXPOSURE CONTROLS/PERSONAL PROTECTION of PEG 120 METHYL GLUCOSE DIOLEATE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
*Body Protection:
Impervious clothing
*Respiratory protection:
Respiratory protection not required.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of PEG 120 METHYL GLUCOSE DIOLEATE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.



STABILITY and REACTIVITY of PEG 120 METHYL GLUCOSE DIOLEATE:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available


PEG 150 DISTEARATE
PEG 150 Distearate is polyethylene glycol diester of stearic acid.
PEG 150 Distearate is in the form of solid, white to off-white waxy flakes and used as a thickener, emulsifier, solubilizer in cosmetics and personal care products.
Typical concentration: 0.5-50%.

CAS: 9005-08-7
MF: C19H40O4
MW: 332.5185

Distearate ester of polyglycol.
PEG-150 Distearate is a polyethylene glycol diester of stearic acid.
HLB 18.9 (gives oil-in-water emulsions).
Appears slightly cloudy in water, but clear in surfactant-containing solutions.
Effective thickener for surfactant-containing products (e.g. shampoo, conditioner, shower gels).
Solubilizer for various water-insoluble ingredients.
Has good co-emulsifying properties in creams & lotions.

PEG 150 Distearate Chemical Properties
Melting point: 35-37 °C
Fp: >230 °F
Odor: at 100.00?%. mild waxy
LogP: 5.997 (est)
CAS DataBase Reference: 9005-08-7
EPA Substance Registry System: PEG 150 Distearate (9005-08-7)

A soft, off-white solid.
PH of 10% dispersion 7.26, saponification number variable.
Soluble in chlorinated solvents, light esters, and acetone; slightly soluble in alcohols, insoluble in glycols, hydrocarbons, and vegetable oils.
PEG 150 Distearate typically is supplied as solid, white to off-white waxy flakes that melt at approximately 52–57°C.
Potential impurities in the raw material can include: unreacted stearic acid or methyl stearate; monofunctional PEG 150 Distearate; unreacted PEG-150; (trans)esterification catalyst residues; trace organic peroxides that result from oxidation of PEG; and 1,4-dioxane, a by-product of ethylene oxide poly-merization to produce PEG-150 diol.
PEG-150 distearate is water-soluble; however, it must be heated above its melting point to achieve effective dissolution and its solubility is tremendously enhanced in the presence of other surfactants.

Uses
PEG 150 Distearate is used as an emulsifier for personal care and water treatment and as a processing aid in textile industry.

Pharmaceutical Applications
PEG 150 Distearate is generally used as emulsifiers in oil-inwater- type creams and lotions.
PEG 150 Distearate's hydrophilicity or lipophilicity depends on the number of ethylene oxide units present: the larger the number, the greater the hydrophilic properties.
PEG 150 Distearate has been used as an emulsifying agent in intravenous infusions.
PEG 150 Distearate is particularly useful as emulsifying agents when astringent salts or other strong electrolytes are present.
PEG 150 Distearate can also be blended with other surfactants to obtain any hydrophilic–lipophilic balance for lotions or ointment formulations.

Production Methods
PEG 150 Distearate is prepared by the direct reaction of fatty acids, particularly stearic acid, with ethylene oxide.

Synonyms
PEG-150 Distearate
6F36Q0I0AC
ETHOX P-6000 DS
PEG-150 DISTEARATE (II)
POLYOXYL 150 DISTEARATE
UNIPEG-6000 DS
DIETHYLENE GLYCOL DISTEARATE
DGD
Polyethyleneglycol3distearate
polyethyleneglycoldistearate#1000
polyglycoldistearate
s1009;s1013
stabogel
PEG 150 DISTEARATE
DESCRIPTION:
PEG-150 Distearate is polyethylene glycol diester of stearic acid.
PEG-150 Distearate is in the form of solid, white to off-white waxy flakes and used as a thickener, emulsifier, solubilizer in cosmetics and personal care products.
Typical concentration of PEG-150 Distearate is 0.5-50%.

CAS Number: 9005-08-7
Chem/IUPAC Name: Poly (oxy-1,2-ethanediyl),. alpha. -(1-oxooctadecyl)-. omega. -[(1-oxooctadecyl)oxy]-


PEG-150 Distearate is a polyethylene glycol diester of stearic acid. HLB 18.9 (gives oil-in-water emulsions).
PEG-150 Distearate Appears slightly cloudy in water, but clear in surfactant-containing solutions.
PEG-150 Distearate is Effective thickener for surfactant-containing products (e.g. shampoo, conditioner, shower gels).

PEG-150 Distearate is Solubilizer for various water-insoluble ingredients.
PEG-150 Distearate Has good co-emulsifying properties in creams & lotions.
PEG-150 Distearate is a polyethylene glycol diester of stearic acid.

PEG-150 Distearate has garnered appreciation for its widespread use in personal care products, cosmetics, paints, and dyes.
PEG-150 Distearate is produced by the esterification of stearic acid which is derived from palm kernel oil or other vegetable oils.


The PEG Distearate ingredients (PEG-2 Distearate, PEG-3 Distearate, PEG-4 Distearate, PEG-6 Distearate, PEG-8 Distearate, PEG-9 Distearate, PEG-12 Distearate, PEG-20 Distearat, PEG-32 Distearate, PEG-75 Distearate, PEG-120 Distearate, PEG-150 Distearate, PEG-175 Distearate) range from liquids to solids or flakes.
In cosmetics and personal care products, PEG Distearate ingredients are used in the formulation of shampoos, hair conditioners, personal cleanliness products, bath products, and skin care and skin cleansing products.

PEG-150 Distearate is an ester made from the reaction of vegetable-derived triple-pressed grade stearic acid and a defined high molecular weight polyethylene glycol.
PEG-150 Distearate is commonly used to thicken mild, amphoteric-containing surfactant systems, such as baby shampoos, baby baths, facial scrubs, facial cleansers, body washes, body scrubs and shaving foams.
PEG-150 Distearate is a Polyethylene glycol diester of stearic acid.
Characteristic odor, slightly cloudy in water, clear in surfactant-containing solutions.

PEG-150 Distearate is an ester made from the reaction of vegetable-derived triple-pressed grade stearic acid.
In addition PEG-150 Distearate is a defined high molecular weight polyethylene glycol.
PEG-150 Distearate is commonly used to thicken mild, amphoteric-containing surfactant systems, such as baby shampoos, baby baths, facial scrubs, facial cleansers, body washes, body scrubs and shaving foams.


USES OF PEG 150 DISTEARATE:
PEG-150 Distearate is used mainly as a thickener in products like shampoos, conditioners, shower gels, face washes, hand washes, shaving creams, baby-care products etc.
Skin care: PEG-150 Distearate is used as an emulsifier in creams and lotions
Hair care: PEG-150 Distearate is used as an anti-static agent in conditioners

PEG-150 Distearate is used to thicken products like shampoos, conditioners, shower gels, hand washes, shaving creams, etc.
PEG-150 Distearate is an excellent emulsifier and is usually added to creams and lotions.
PEG-150 Distearate mixes well with water and oil and enables them to clean dirt and grime from the surface.

PEG-150 Distearate forms a film on the hair and reduces static and is therefore used in conditioners.
When added to paints and dyes, it thickens their consistency and emulsifies them.

PEG-150 Distearate is a cosmetic chemical used in cleansing products, personal care products, etc. Gincol PEGDS6 with a chemical name PEG-150 Distearate acts as an emollient as well as a viscosity modifier.
The properties of PEG-150 Distearate include being an effective emulsifier and thickening agent for surfactant-containing hair care products such as shampoos, and shower gels.

Its usage can also be seen in other cosmetic applications such as baby bath products, conditioners, body creams, and lotions.

HOW IT WORKS
PEG-150 Distearate works by acting as a solubilizer for water-insoluble ingredients.
PEG-150 Distearate reduces the surface tension of the substances and helps form emulsions.

CONCENTRATION AND SOLUBILITY-
PEG-150 Distearate is used at a concentration of 0.5% to 5% of the formulation.
PEG-150 Distearate is soluble in water and ethanol and is insoluble in vegetable and mineral oil.

HOW TO USE
Heat it with other surfactants at 60oC and melt PEG-150 Distearate completely.
Mix this blend into the water phase at 35oC and stir.
Add oil phase and adjust the pH.





Origin:
PEG-150 Distearate is produced by the esterification of stearic acid which is derived from palm kernel oil or other vegetable oils.

WHAT DOES PEG-150 DISTEARATE DO IN A FORMULATION?
• Emulsifying
• Viscosity controlling


BENEFITS OF PEG-150 DISTEARATE:
PEG-150 Distearate, since has water-loving PEG and Oil-loving stearic acid, can be used as an emulsifier and thickening agent.
PEG is relatively a bulky molecule, plus it has various chemical groups attached that can attract and hold water molecules together.
So in a formulation, PEG-150 Distearate can increase thickness because of this swelling of the molecule.

Also, as a thickener, PEG-150 Distearate stabilizes the product and enhances its overall performance on the skin.
Moreover, PEG-150 Distearate also acts as an emulsifier, which gives stability to the product and prevents the oil and water-based components of the product from getting separated.
PEG-150 Distearate also functions as a surfactant and forms the base of many cleansing products.

PEG-150 Distearate mixes with water and oil present on the skin with the dirt.
The dirt gets rinsed off easily from the skin water.
PEG-150 Distearate is used in shampoos, conditioners, bath products, and other personal care products.








CHEMICAL AND PHYSICAL PROPERTIES OF PEG-150 DISTEARATE:

Boiling Point 492-497°C
Melting Point 52-57°C
Hydroxyl Value 5 max.
Solubility Soluble in water and ethanol
Insoluble in mineral and vegetable oil
Saponification Value: 165-175 mgKOH/g
INCI
PEG-150 distearate
Appearance
White flake
Usage rate
Heat to 60°C (140°F) when incorporating into formulas. Typical use level 0.5 - 5% (even at low levels there is a thickening effect). For external use only.
Applications Shampoo, conditioner, shower gels, baby shampoo, bubble bath, creams, lotions & other emulsions.
Scent Nothing much
Solubility: Soluble in water
Why do we use it in formulations?:
Effective thickener for surfactant-containing products (e.g. shampoo, conditioner, shower gels),
Benefits:
Effective thickener for surfactant-containing products (e.g. shampoo, conditioner, shower gels)
Solubilizer for various water-insoluble ingredients
Has good co-emulsifying properties in creams & lotions
Chemical Name/INCI Name PEG 150 Distearate
Nature of Emollient Conditioner & Emollient
Active Level Min 98%
Uses
Usage 1% to 2%
Skin care- face care and cosmetics
Body care
Hair care
Special Feature Viscosity Modifier and Emollient
Use: For adding viscosity (thickener) to liquid soap. face wash cleanser shampoo
Mixing method: mix in water or in the detergent part Reheat them to melt. and stir to combine
Usage rate: 1-5% (according to the desired viscosity, 1-3% recommended)
Product characteristics: White-light granular powder
Solubility: can be dissolved in water with heat
Storage: can be stored at room temperature but close the lid of the bottle tightly and protected from sunlight, humidity or heat, the product has a shelf life of at least 2 years
INCI Name : PEG-150 Distearate



SAFETY INFORMATION ABOUT PEG 150 DISTEARATE:
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product







SYNONYMS OF PEG 150 DISTEARATE:
PEG-150 Distearate
6F36Q0I0AC
ETHOX P-6000 DS
PEG-150 DISTEARATE (II)
POLYOXYL 150 DISTEARATE
UNIPEG-6000 DS