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OLEYL ALCOHOL 5 EO
Oleyl Alcohol 5 EO Oleyl alcohol 5 EO /ˈoʊliˌɪl, ˈoʊliəl/,[1] octadecenol /ˌɒktəˈdɛsɪˌnɒl/, or cis-9-octadecen-1-ol, is an unsaturated fatty alcohol with the molecular formula C18H36O or the condensed structural formula CH3(CH2)7-CH=CH-(CH2)8OH. It is a colorless oil, mainly used in cosmetics.[2] Oleyl alcohol 5 EO can be produced by the hydrogenation of oleic acid esters by Bouveault–Blanc reduction, which avoids reduction of the C=C group (as would occur with usual catalytic hydrogenation). The required oleate esters are obtained from beef fat, fish oil, and, in particular, olive oil (from which it gains its name). The original procedure was reported by Louis Bouveault in 1904[3] and subsequently refined. Oleyl alcohol 5 EO has uses as a nonionic surfactant, emulsifier, emollient and thickener in skin creams, lotions and many other cosmetic products including shampoos and hair conditioners. It has also been investigated as a carrier for delivering medications through the skin or mucus membranes; particularly the lungs. Oleic acid - the corresponding fatty acid Oleylamine - the corresponding amine Oleamide - the corresponding amide Oleyl alcohol 5 EO, or cis-9-octadecen-1-ol, is an unsaturated fatty alcohol with the molecular formula C18H36O or the condensed structural formula CH3(CH2)7-CH=CH-(CH2)8OH.It can be produced by the hydrogenation of oleic acid esters; which can be obtained naturally from beef fat, fish oil and in particular oliveoil (from which it gains its name). Production by the Bouveault-Blanc reduction of ethyl oleate or n-butyl oleate esters was reported by Louis Bouveault in1904 and subsequently refined.It has uses as a nonionic surfactant, emulsifier, emollient and thickener in skin creams, lotions and many other cosmeticproducts including shampoos and hair conditioners. It has also been investigated as a carrier for delivering medications through the skin or mucus membranes;particularly the lungs.It is a non-ionic, unsaturated fatty alcohol. It has uses as a nonionic surfactant, emulsifier, emollient and thickener in skincreams, lotions Oleyl alcohol 5 EO and Octyldodecanol are long chain fatty alcohols. Stearyl Alcohol is a white, waxy solid with a faint odor, while Oleyl alcohol 5 EO and Octyldodecanol are clear, colorless liquids. These three ingredients are found in a wide variety of products such as hair conditioners, foundations, eye makeup, skin moisturizers, skin cleansers and other skin care products.Oleyl alcohol 5 EO and Octyldodecanol help to form emulsions and prevent an emulsion from separating into its oil and liquid components. These ingredients also reduce the tendency of finished products to generate foam when shaken. When used in the formulation of skin care products, Stearyl Alcohol, Oleyl alcohol 5 EO and Octyldodecanol act as a lubricants on the skin surface, which gives the skin a soft, smooth appearance. Uses Oleyl alcohol 5 EO is a nonionic surfactant used as a hair coating in shampoos and conditioners.Oleyl alcohol 5 EO is used as an emollient (skin softener), emulsifier, and thickener in creams and lotions. Oleyl alcohol 5 EO, octadecenol, or cis-9-octadecen-1-ol, is a fatty alcohol coming from inedible beef fat. It is also found in fish oil. Its chemical formula is C18H36O or CH3(CH2)7-CH=CH-(CH2)8OH. It is a non-ionic, unsaturated fatty alcohol. It has uses as a nonionic surfactant, emulsifier, emollient and thickener in skin creams, lotions and many other cosmetic products, plasticizer for softening fabrics, surfactant and hair coating in shampoos and hair conditioners, and a carrier for medications. Oleyl alcohol 5 EO is classified under CAS No.143-28-2.Oleyl alcohol 5 EO is also known as cis-9-octadecen-1-ol.Oleyl alcohol 5 EO is a non-ionic, unsaturatedfatty alcohol, a long-chain aliphatic alcohol that occurs naturally in fish oils.Oleyl alcohol 5 EO prepared by synthetic reduction of plant-derived oleic acid. Oleyl alcohol 5 EO can be used in large scale applications as the softening and lubrication of textile fabrics, and in production of carbon paper,stencil paper, and printing ink.Oleyl alcohol 5 EO also utilized as an antifoam agent and cutting lubricant.Oleyl alcohol 5 EO also known as precursor for the preparation of its sulfuric ester derivatives, which are used in detergents and wetting agents.Oleyl alcohol 5 EO has also been incorporated into various formulations for drug delivery.Oleyl alcohol 5 EO can also be used as a non-ionicsurfactant, emulsifier, emollient and thickener in skin creams, lotions and many othercosmetic products. Oleyl alcohol 5 EO also used as plasticizer for softening fabrics, surfactant and hair coating in shampoos and hair conditioners, and a carrier for medications. Oleyl alcohol 5 EO (also octadecenol or cis-9-octadecen-1-ol) is a non-ionic, unsaturated fatty alcohol. It is an emulsion stabilizer, antifoam agent, detergent, and release agent for food applications. Oleyl alcohol 5 EO is found in fish oils and inedible beef fat. It belongs to the family of fatty alcohols. These are aliphatic alcohols consisting of a chain of 8 to 22 carbon atoms (do not have to bear a carboxylic acid group Substituents Long chain fatty alcohol Organic oxygen compound Hydrocarbon derivative Primary alcohol Organooxygen compound Alcohol Aliphatic acyclic compound Stearyl Alcohol, Oleyl alcohol 5 EO, and Octyl Dodecanol are long-chain saturated or unsaturated (Oleyl) fatty alcohols. They are used in numerous cosmetic product categories at concentrations of less than 0.1 percent to greater than 50 percent.The metabolism of Stearyl Alcohol and Oleyl alcohol 5 EO in rats is described. The results of acute oral toxicity studies indicate a very low order of toxicity. In rabbit irritation tests, these alcohols produced minimal ocular irritation and minimal to mild cutaneous irritation. Stearyl Alcohol produced no evidence of contact sensitization or comedogenicity.Clinical patch testing indicates a very low order of skin irritation potential and sensitization. Photoreactivity studies on products containing these ingredients were negative for phototoxicity or photosensitization.Based on the available data, it is concluded that Stearyl Alcohol, Oleyl alcohol 5 EO, and Octyl Dodecanol are safe as currently used in cosmetics. Applications Oleyl alcohol 5 EO is used in softening and lubrication of textile fabrics, and in the production of carbon paper, stencil paper, and printing ink. It finds application in cosmetic products viz skin creams and lotions as a thickner, hair conditioners and hair coating shampoos. It is utilized as an antifoaming agent and cutting lubricant, as the precursor for the preparation of its sulfuric ester derivatives, which are used in detergents and wetting agents. It plays a vital role in various formulations for drug delivery. Occurs in fish oils. Emulsion stabiliser, antifoam agent, detergent and release agent for food applications Oleyl alcohol 5 EO, octadecenol, or cis-9-octadecen-1 -ol, is a fatty alcohol coming from inedible beef fat. It is also found in fish oil. Oleyl alcohol 5 EO is used in softening and lubrication of textile fabrics, and in the production of carbon paper, stencil paper, and printing ink. It finds application in cosmetic products viz skin creams and lotions as a thickner, hair conditioners and hair coating shampoos. It is utilized as an antifoaming agent and cutting lubricant, as the precursor for the preparation of its sulfuric ester derivatives, which are used in detergents and wetting agents. It plays a vital role in various formulations for drug delivery. Solubility Miscible with alcohol and ether. Slightly miscible with carbon tetrachloride. Immiscible with water. Oleyl alcohol 5 EO is a fatty alcohol which is usually found in fish oil and beef fat. It is unsaturated and non-ionic in nature which shares a wide scope in various application as well as end-user industries. Oleyl alcohol 5 EO is used in an extensive range of applications such as lotions, thickener in skin creams, emulsifiers, surfactants, hair coatings, hair conditioners, and plasticizers for softening fabrics. The global market for Oleyl alcohol 5 EO has been witnessing significant growth on account of increasing demand from its application industries such as personal care. It is used in a variety of applications such as surfactants, pharmaceuticals and cosmetics. One of the major opportunities for the surfactant industry is bio-based surfactants where rising awareness among consumers towards eco-friendly products has noticeably contributed towards the growing demand for Oleyl alcohol 5 EO in surfactants. Surfactants also share a broad application scope as foaming agents, emulsifiers, detergents, and wetting agents. Conditioning and detergency are some of the vital properties of surfactants due to which they share a wide application scope. Major applications of Oleyl alcohol 5 EO-based surfactants include personal care, textile, pharmaceutical, soap and detergent among others. Key manufacturers have entered into several collaborations and agreements with other companies for the marketing of new products as well as garnering a larger share in the market. Other applications of Oleyl alcohol 5 EO include plasticizer for use in fabrics. The market for Oleyl alcohol 5 EO in plasticizers has been witnessing noticeable growth due to changing lifestyles and emerging global economies in Asia Pacific and Latin America. Additionally, growing environmental awareness and rising legal provisions have been serving as a catalyst for the plasticizers market with developments in various emerging economies such as Brazil, Russia, China and India. Matured regions such as Europe and North America accounted for the highest demand for Oleyl alcohol 5 EO due to the presence of vast hair care and skin care industries in these regions resulting in significant demand for the chemical. Moreover, emerging economies in Asia Pacific such as Japan, China and India are anticipated to witness the fastest growth rate over the forecast period on account of growing hair care, skin care and pharmaceutical industries in the region. Various factors such as rising awareness regarding healthy hair and skin among consumers as well as changing lifestyles is expected to boost the demand for personal care products which in turn is anticipated to contribute towards the demand for Oleyl alcohol 5 EO. Increased demand for personal care products such as hair care and skin care is expected to be another important factor that triggers the need for Oleyl alcohol 5 EO, due to increased awareness of hair and skin. In addition, the increasing demand for drugs is also expected to contribute to the increased demand for Oleyl alcohol 5 EO in the production of various drugs and ointments during the forecast period. In addition, due to low cost and ease of use, the increase in alcohol consumption in surfactants has contributed significantly to the growth of the market. However, fluctuating prices of major raw materials have been a major concern for producers and are expected to limit the growth of the market. Oleyl alcohol 5 EO focusing on the commercialization and development of cost-effective bio-based surfactants, is expected to provide new opportunities for the growth of the market. Oleyl alcohol 5 EO It is a clear, colorless liquid. It is found in a wide variety of products such as hair conditioners, skin moisturizers, skin cleansers and other skin care products.Oleyl alcohol 5 EO helps to form emulsions and prevent an emulsion from separating into its oil and liquid components. When used in the formulation of skin care products, it acts as a lubricants on the skin surface, which gives the skin a soft, smooth appearance.Increasing demand for personal care products such as hair care and skin care on account of rising awareness for hair and skin is expected to be another major factor driving the demand for Oleyl alcohol 5 EO. Moreover, growing demand for pharmaceuticals is also expected to contribute towards the growing demand for Oleyl alcohol 5 EO in the production of various drugs and ointments within the forecast period. In addition, increasing consumption of Oleyl alcohol 5 EO in surfactants due to their low cost and ease of availability has also contributed significantly towards the growth of the market. However, fluctuating prices of key feedstock materials has been major concern for the manufacturers and is expected to limit the growth of the market. Focus on commercializing and developing cost-effective bio-based surfactants using Oleyl alcohol 5 EO is anticipated to provide new opportunities for the growth of the market. Oleyl alcohol 5 EO Usage Oleyl alcohol 5 EO is used in the treatment, control, prevention of the following diseases, conditions and symptoms: Psoriasis Seborrheic dermatitis Skin creams and lotions thickener Hair softening Oleyl alcohol 5 EO - Side effects It is a list of possible side effects from the medicines containing Oleyl alcohol 5 EO. This is not a comprehensive list. These side effects are likely to be seen, but not always. Some of the side effects are rare, but they can be very serious. Consult your doctor if you observe any of the following side effects, especially those that do not persist despite your waiting period. Skin irritation Irritation of the head skin Skin / hair coloring Oleyl alcohol 5 EO Study, Action Mechanism and Pharmacology Oleyl alcohol 5 EO improves the condition of the patient by performing the following functions: The skin is causing dead cells from the upper layer. Inhibit phosphatidylcholine synthesis. Oleyl alcohol 5 EO, or cis-9-octadecen-1-ol, is an unsaturated fatty alcohol with the molecular formula C18H36O or the condensed structural formula CH3(CH2)7-CH=CH-(CH2)8OH.It can be produced by the hydrogenation of oleic acid esters; which can be obtained naturally from beef fat, fish oil and in particular oliveoil (from which it gains its name). Production by the Bouveault-Blanc reduction of ethyl oleate or n-butyl oleate esters was reported by Louis Bouveault in1904 and subsequently refined.It has uses as a nonionic surfactant, emulsifier, emollient and thickener in skin creams, lotions and many other cosmeticproducts including shampoos and hair conditioners. It has also been investigated as a carrier for delivering medications through the skin or mucus membranes;particularly the lungs.It is a non-ionic, unsaturated fatty alcohol. It has uses as a nonionic surfactant, emulsifier, emollient and thickener in skincreams, lotions Oleyl alcohol 5 EO and Octyldodecanol are long chain fatty alcohols. Stearyl Alcohol is a white, waxy solid with a faint odor, while Oleyl alcohol 5 EO and Octyldodecanol are clear, colorless liquids. These three ingredients are found in a wide variety of products such as hair conditioners, foundations, eye makeup, skin moisturizers, skin cleansers and other skin care products.Oleyl alcohol 5 EO and Octyldodecanol help to form emulsions and prevent an emulsion from separating into its oil and liquid components. These ingredients also reduce the tendency of finished products to generate foam when shaken. When used in the formulation of skin care products, Stearyl Alcohol, Oleyl alcohol 5 EO and Octyldodecanol act as a lubricants on the skin surface, which gives the skin a soft, smooth appearance. Uses Oleyl alcohol 5 EO is a nonionic surfactant used as a hair coating in shampoos and conditioners.Oleyl alcohol 5 EO is used as an emollient (skin softener), emulsifier, and thickener in creams and lotions. Oleyl alcohol 5 EO, octadecenol, or cis-9-octadecen-1-ol, is a fatty alcohol coming from inedible beef fat. It is also found in fish oil. Its chemical formula is C18H36O or CH3(CH2)7-CH=CH-(CH2)8OH. It is a non-ionic, unsaturated fatty alcohol. It has uses as a nonionic surfactant, emulsifier, emollient and thickener in skin creams, lotions and many other cosmetic products, plasticizer for softening fabrics, surfactant and hair coating in shampoos and hair conditioners, and a carrier for medications. (9Z)-octadecen-1-ol is a long chain fatty alcohol that is octadecanol containing a double bond located at position 9 (the Z-geoisomer). It has a role as a nonionic surfactant and a metabolite. It is a long-chain primary fatty alcohol and a fatty alcohol 18:1. A mixture of cis-9[1(-14)C] octadecenol and [1(-14)C] docosanol was injected into the brains of 19-day-old rats, and incorporation of radioactivity into brain lipids was determined after 3, 12, and 24 hr. Both alcohols were metabolized by the brain but at different rates; each was oxidized to the corresponding fatty acid, but oleic acid was more readily incorporated into polar lipids. Substantial amounts of radioactivity were incorporated into 18:1 alkyl and alk-1-enyl moieties of the ethanolamine phosphoglycerides and into 18:1 alkyl moieties of the choline phosphoglycerides. Even after the disappearance of the 18:1 alcohol from the substrate mixture (12 hr), the 22:0 alcohol was not used to any measurable extent for alkyl and alk-1-enylglycerol formation. cis-9-Octadecenyl alcohol (Oleyl alcohol 5 EO), orally administered, increased the relative concentration of 18:1 alkyl and alk-1-enyl moieties in alkoxylipids of the small intestine of rats. Farnesol (FOH) inhibits the CDP-choline pathway for PtdCho (phosphatidylcholine) synthesis, an activity that is involved in subsequent induction of apoptosis /SRP: programmed cell death/. Interestingly, the rate-limiting enzyme in this pathway, CCTalpha (CTP:phosphocholine cytidylyltransferase alpha), is rapidly activated, cleaved by caspases and exported from the nucleus during FOH-induced apoptosis. The purpose of the present study was to determine how CCTalpha activity and PtdCho synthesis contributed to induction of apoptosis by FOH and Oleyl alcohol 5 EO. Contrary to previous reports, /the authors/ show that the initial effect of FOH and Oleyl alcohol 5 EO was a rapid (10-30 min) and transient activation of PtdCho synthesis. During this period, the mass of DAG (diacylglycerol) decreased by 40%, indicating that subsequent CDP-choline accumulation and inhibition of PtdCho synthesis could be due to substrate depletion. At later time points (>1 h), FOH and Oleyl alcohol 5 EO promoted caspase cleavage and nuclear export of CCTalpha, which was prevented by treatment with oleate or DiC8 (dioctanoylglycerol). Protection from FOH-induced apoptosis required CCTalpha activity and PtdCho synthesis since (i) DiC8 and oleate restored PtdCho synthesis, but not endogenous DAG levels, and (ii) partial resistance was conferred by stable overexpression of CCTalpha and increased PtdCho synthesis in CCTalpha-deficient MT58 cells. These results show that DAG depletion by FOH or Oleyl alcohol 5 EO could be involved in inhibition of PtdCho synthesis. However, decreased DAG was not sufficient to induce apoptosis provided nuclear CCTalpha and PtdCho syntheses were sustained. Residues of Oleyl alcohol 5 EO are exempted from the requirement of a tolerance when used as a cosolvent (limit: 15%) in accordance with good agricultural practice as inert (or occasionally active) ingredients in pesticide formulations applied to growing crops or to raw agricultural commodities after harvest. Hydrophilic and lipophilic formulations of naproxen were prepared, and the influence of the excipients in the formulations on the ulcerogenic potential of naproxen was investigated in rats. Doses of naproxen suspensions ranging from 3.125-100 mg/kg were administered to fasted rats and excised stomachs were examined macroscopically for the incidence and severity of lesions. Results were expressed as the 50% ulceration dose. Results of the study showed that a lipophilic formulation containing Oleyl alcohol 5 EO provided the greatest gastric protection. Long-chain fatty acids are important nutrients, but obesity is the most common nutritional disorder in humans. In this study /the authors/ investigated the effect of Oleyl alcohol 5 EO on the intestinal long-chain fatty acid absorption in rats. ...[14C]Oleic acid and Oleyl alcohol 5 EO /was administered/ as lipid emulsion intraduodenally in unanesthetized lymph-cannulated rats and measured the lymphatic output of oleic acid. ... Lipid emulsion /was then administered/ with a stomach tube and ... the luminal and mucosal oleic acid residues /were measured/. Furthermore, rats were fed Oleyl alcohol 5 EO as a dietary component for 20 days, and fecal lipid and the weight of adipose tissues were measured. In lymph-cannulated rats, triglyceride and [14C]oleic acid output in the lymph were significantly lower in the presence of Oleyl alcohol 5 EO when compared with the absence of Oleyl alcohol 5 EO in a dose-dependent manner. The radioactivity remaining in the intestinal lumen was more strongly detected in rats that had been orally administered Oleyl alcohol 5 EO than in the controls. The feces of rats fed an oleyl-alcohol-added diet contained much higher amounts of lipids, and the weights of their adipose tissues were significantly lower than in the control group. These results suggest that Oleyl alcohol 5 EO inhibits the rat gastrointestinal absorption of long-chain fatty acids in vivo. Studies of the influence of fatty acids, which were the component of intestinal mucosal lipids, on the permeability of several drugs across bilayer lipid membranes generated from egg phosphatidylcholine and intestinal lipid have been pursued. The permeability coefficients of p-aminobenzoic acid, salicylic acid and p-aminosalicylic acid (anionic-charged drug) increased when fatty acids such as lauric, stearic, oleic, linoleic and linolenic acid were incorporated into the bilayer lipid membranes generated from phosphatidylcholine. In the presence of methyl linoleate and Oleyl alcohol 5 EO, no enhancing effect on p-aminobenzoic acid transfer was obtained. The effect of fatty acids was more marked at pH 6.5 than at pH 4.5. In contrast, upon the addition of fatty acids to intestinal lipid membranes which originally contained fatty acids, the permeability coefficient of p-aminobenzoic acid tended to decrease, though the permeability through intestinal lipid membranes was larger than that of phosphatidylcholine membranes. The permeability of p-aminobenzoic acid across bilayer lipid membranes from intestinal phospholipids was significantly decreased to about equal that of phosphatidylcholine membranes, and reverted to the value of intestinal lipid membranes when fatty acids were added to intestinal phospholipids. It seemed reasonable to assume that free fatty acids in the intestinal neutral lipid fraction could contribute to the increase in the permeability of p-aminobenzoic acid. On the basis of above results, possible mechanisms for good absorbability of weakly acidic drugs from the intestine are discussed. The aim of this study was to investigate the frequency of sensitization to fatty alcohols in a group of patients with suspected cosmetic or medicament contact dermatitis. From May 1992 to September 1995, we patch tested a series of 5 fatty alcohols on 146 patients. These included 108 females and 38 males aged from 13 to 72 years (mean age 42.5). These patients, who had previously been tested with the GIRDCA standard series, were selected because their clinical lesions or histories indicated topical preparations as the possible source of their contact dermatitis. High-grade fatty alcohols (> 99% pure) were used for testing. 34 patients (23.2%), 25 female and 9 male aged from 14 to 72 years, showed a positive patch test to fatty alcohols, 33 of them to Oleyl alcohol 5 EO. A total of 39 reactions were detected with 5 patients showing more than 1 positive reaction. Our results show that sensitization to Oleyl alcohol 5 EO is not rare in patients with contact dermatitis due to cosmetics or topical medicaments. Acute Exposure/ ... Up to 50% glycerol, 10% hydroxyethyl lactamide (HELA), 10% Oleyl alcohol 5 EO, 10% Solketal, 10% glycofurol, 100% tetrahydrofurfuryl alcohol (THFA) and 10% urea induced no discernible change in the histological appearance of the skin whereas 100% dimethyl sulphoxide (DMSO), 100% dimethyl formamide (DMF), 100% N-methyl-2-pyrrolidone, 10% Azone, 10% oleic acid, 10% methyl laurate, 10% benzyl alcohol and 10% glycerol formal caused severe skin irritation. Subchronic or Prechronic Exposure/ ... In lymph-cannulated rats, triglyceride and [14C]oleic acid output in the lymph were significantly lower in the presence of Oleyl alcohol 5 EO when compared with the absence of Oleyl alcohol 5 EO in a dose-dependent manner. The radioactivity remaining in the intestinal lumen was more strongly detected in rats that had been orally administered Oleyl alcohol 5 EO than in the controls. The feces of rats fed an oleyl-alcohol-added diet contained much higher amounts of lipids, and the weights of their adipose tissues were significantly lower than in the control group. Three unsaturated fatty alcohols at 35-50 microM inhibited DNA synthesis and the proliferation of tumor cells by a combination with hyperthermia to greater extents in the order: oleyl (C18:1)-> linoleyl (C18:2)-> alpha-linolenyl (C18:3) alcohol. Two saturated fatty alcohols, palmityl (C16:0)- and stearyl (C18:0) alcohols, did not inhibit at the same concentrations. At 100 microM, palmityl alcohol inhibited, whereas stearyl alcohol did not. ... The inhibition of the unsaturated fatty alcohols on DNA synthesis and proliferation was nearly proportional to the amount of their intercellular accumulation at 37 degrees C or 42 degrees C; the most inhibitory, Oleyl alcohol 5 EO, was the most membrane-permeable, whilst inversely the least inhibitory, alpha-linolenyl alcohol, was the least permeable. A proportional correlation was not observed for saturated fatty alcohols Oleyl alcohol 5 EO's use as a chemical intermediate, automotive lubricant, defoamer, cosolvent and plasticizer for printing ink, and as a cosmetic emollient may result in its release to the environment through various waste streams. Oleyl alcohol 5 EO is a natural product in fish oils. If released to the air, an estimated vapor pressure of 9.3X10-5 mm Hg at 25 °C indicates Oleyl alcohol 5 EO will exist in both the vapor and particulate-phases in the atmosphere. Vapor-phase Oleyl alcohol 5 EO 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 4.9 hours and ozone radicals in the troposphere with an estimated half-life of 2.1 hours. Particulate-phase Oleyl alcohol 5 EO will be removed from the atmosphere by wet or dry deposition. If released to soil, Oleyl alcohol 5 EO is expected to have no mobility based upon an estimated Koc of 1.3X10+4. Volatilization from moist soil surfaces is expected to be an important fate process based upon an estimated Henry's Law constant of 4.6X10-4 atm-cu m/mole. However, adsorption to soil is expected to attenuate volatilization. One microbial study which used pure cultures suggests that biodegradation may be an important fate process of Oleyl alcohol 5 EO in soil and water, but no rate data are available. If released to water, Oleyl alcohol 5 EO is expected to adsorb to suspended solids and sediment based upon the estimated Koc. 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 8 hours and 7.4 days, respectively. However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column. The estimated volatilization half-life from a model pond is 163 days if adsorption is considered. An estimated BCF of 420 suggests the potential for bioconcentration in aquatic organisms is high. 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 Oleyl alcohol 5 EO may occur through inhalation of vapors or through eye and dermal contact with this compound at workplaces where Oleyl alcohol 5 EO is produced or used. The general public may be exposed to Oleyl alcohol 5 EO by dermal contact during the use of cosmetics in which it is contained as a cosmetic emollient and through fish consumption. Oleyl alcohol 5 EO's use as a chemical intermediate, automotive lubricant, defoamer, cosolvent and plasticizer for printing ink, and as a cosmetic emollient(1) may result in its release to the environment through various waste streams(SRC). Based on a classification scheme(1), an estimated Koc value of 1.3X10+4(SRC), determined from a structure estimation method(2), indicates that Oleyl alcohol 5 EO is expected to be immobile in soil(SRC). Volatilization of Oleyl alcohol 5 EO from moist soil surfaces may be expected to be an important fate process(SRC) given an estimated Henry's Law constant of 4.6X10-4 atm-cu m/mole(SRC), using a fragment constant estimation method(3). Oleyl alcohol 5 EO is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 9.3X10-5 mm Hg(SRC), determined from a fragment constant method(4). However, adsorption to soil is expected to attenuate volatilization(SRC). Based on one microbial study, Oleyl alcohol 5 EO was found to be utilized as the sole carbon source by bacteria, yeast, and fungi(5). Although this study provides little insight into the rate of biodegradation in soil, it suggests that biodegradation in soil may be important(SRC). Based on a classification scheme(1), an estimated Koc value of 1.23X10+4(SRC), determined from a structure estimation method(2), indicates that Oleyl alcohol 5 EO is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 4.6X10-4 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 8 hours and 7.4 days, respectively(SRC). However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column. The estimated volatilization half-life from a model pond is 163 days if adsorption is considered(5). Alcohols are generally resistant to hydrolysis(6). According to a classification scheme(7), an estimated BCF of 420(SRC), from an estimated log Kow of 7.5(8) and a regression-derived equation(9), suggests the potential for bioconcentration in aquatic organisms is high(SRC). Based on one microbial study, Oleyl alcohol 5 EO was found to be utilized as the sole carbon source by bacteria, yeast, and fungi(10). Although this study provides little insight into the rate of biodegradation in water, it suggests that biodegradation in water may be important(SRC). ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), Oleyl alcohol 5 EO, which has an estimated vapor pressure of 9.3X10-5 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase Oleyl alcohol 5 EO 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 4.5 hrs(SRC), calculated from its rate constant of 7.8X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Particulate-phase oleyl alchol may be removed from the air by wet or dry deposition(SRC). The rate constant for the vapor-phase reaction of Oleyl alcohol 5 EO with ozone has been estimated as 1.3X10-16 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). This corresponds to an atmospheric half-life of about 2.1 hrs at an atmospheric concentration of 7X10+11 ozone molecules per cu cm(4). AEROBIC: Oleyl alcohol 5 EO (10 g) was found to be utilized as the sole carbon source by bacteria (Pseudomonas) in 10 days at 30 °C and pH 6.8-7.0. In the same study, 10 g Oleyl alcohol 5 EO was utilized as the sole carbon source by 3 yeasts (Candida, Pichia, and an unknown) in 10 days at 30 °C and pH 6.8-7.0. It was also utilized by 3 fungi (Aspergillus, Penicillium, and an unknown) in 20 days at 20-25 °C and pH 5.5
OLEYL AMINE ETHOXYLATED 
1-Amino-9-octadecene; Oleinamine; 9-octadecenylamine; (Z)-9-Octadecen-1-amine; Oleamine; Oleylamin (German); cas no: 112-90-3
OLEYL AMINE  
oleyl amine oxide 2 eo; Oleylamine with 2 mol EO; Oleyl Amin Etoksilatlar; Coco Amin Etoksilatlar; Oleyl alcohol ethoxylate 2 EO; Tallow Amine Ethoxylate; cas no: 26635-93-8
oleyl amine oxide 2 eo
oleyl amine oxide 2 eo; Oleylamine with 2 mol EO; Oleyl Amin Etoksilatlar; Coco Amin Etoksilatlar; Oleyl alcohol ethoxylate 2 EO; Tallow Amine Ethoxylate; cas no: 26635-93-8
OLEYL CETYL ALCOHOL 30/70
Oleyl Cetyl Alcohol 30/70 Oleyl cetyl alcohol 30/70, Ceto Stearyl Alcohol or cetearyl alcohol is a mixture of fatty alcohols, consisting predominantly of cetyl (16 C) and stearyl alcohols (18 C) and is classified as a fatty alcohol. . Oleyl cetyl alcohol 30/70 is used as an emulsion stabilizer, Oleyl cetyl alcohol 30/70 is used as opacifying agent, and Oleyl cetyl alcohol 30/70 is used as foam boosting surfactant, as well as an aqueous and Oleyl cetyl alcohol 30/70 is used as nonaqueous viscosity-increasing agent. Oleyl cetyl alcohol 30/70 imparts an emollient feel to the skin and can be used in water-in-oil emulsions, oil-in-water emulsions, and anhydrous formulations. Oleyl cetyl alcohol 30/70 is commonly used in hair conditioners and other hair products. What is Oleyl cetyl alcohol 30/70 used for? Oleyl cetyl alcohol 30/70 is used as an emulsion stabilizer, Oleyl cetyl alcohol 30/70 is used as opacifying agent, and Oleyl cetyl alcohol 30/70 is used as foam boosting surfactant, as well as an aqueous and nonaqueous viscosity-increasing agent. Oleyl cetyl alcohol 30/70 imparts an emollient feel to the skin and Oleyl cetyl alcohol 30/70 can be used in water-in-oil emulsions, oil-in-water emulsions, and anhydrous formulations. Oleyl cetyl alcohol 30/70 is a chemical found in cosmetic products Oleyl cetyl alcohol 30/70 is a white, waxy substance made from cetyl alcohol and stearyl alcohol, both fatty alcohols. Oleyl cetyl alcohol 30/70 is found in animals and plants, like coconut and palm oil. Oleyl cetyl alcohol 30/70 can also be made in a laboratory. Chemical name : Oleyl/ Cetyl alcohol 30/70 chemical name : Oleyl/ Cetyl alcohol 30/70 Appearance : white solid assay : C16: 10-25 %; C18: 70-90 % other : Hydroxyl value: 208-218 mgKOH/g Acid value: max 0,2mgKOH/g Saponification Value: max. 1 mg KOH/g Moisture : max 0,1 % Density : ca. 0,825 / 40 °C Packing : drums Einecs : 268-106-1 CAS No. : 68002-94-8 Synonym : Fettalkohol C 16/ C 18 und C 18 ungesättigt Product categories : alcohols, Oleyl cetyl alcohol 30/70 is used in personal care products, Oleyl cetyl alcohol 30/70 is used in mainly skin lotions, Oleyl cetyl alcohol 30/70 is used in hair products, and Oleyl cetyl alcohol 30/70 is used in creams. Oleyl cetyl alcohol 30/70 help create smoother creams, thicker lotions, and more stable foam products. Oleyl cetyl alcohol 30/70 are sometimes called long-chain alcohols because of their chemical formula. Oleyl cetyl alcohol 30/70 usually has an even number of carbon atoms, with a single alcohol group (–OH) attached to the last carbon. Cetyl alcohol has 16 carbon atoms. Stearyl alcohol has 18. Oleyl cetyl alcohol 30/70 is a combination of the two, so it has 34 carbon atoms. Oleyl cetyl alcohol 30/70 ’s molecular formula is C34H72O2. Oleyl cetyl alcohol 30/70 helps prevent creams from separating into oil and liquid. A chemical that helps to keep liquid and oil together is known as an emulsifier. Oleyl cetyl alcohol 30/70 may also make a product thicker or increase the product’s ability to foam. skin lotions. Oleyl cetyl alcohol 30/70 is used in moisturizers. Oleyl cetyl alcohol 30/70 is used in skin creams. Oleyl cetyl alcohol 30/70 is used in sunscreen. Oleyl cetyl alcohol 30/70 is used in shampoo. Oleyl cetyl alcohol 30/70 is used in conditioners. Oleyl cetyl alcohol 30/70 is used in hair removal creams. Oleyl cetyl alcohol 30/70 is used in hair mousse. Oleyl cetyl alcohol 30/70 is used in anti-frizz hair cream. Oleyl cetyl alcohol 30/70 is used in hair dye. Oleyl cetyl alcohol 30/70 is used in mascara. Oleyl cetyl alcohol 30/70 most often appears on the ingredient list as Oleyl cetyl alcohol 30/70 , but may have many other names. Oleyl cetyl alcohol 30/70 isn’t the only fatty alcohol used in cosmetic products. Other examples include cetyl alcohol, lanolin, oleyl alcohol, and stearyl alcohol. Oleyl cetyl alcohol 30/70 is used to help soften the skin and hair and to thicken and stabilize cosmetic products, such as lotions and hair products. As an emollient, Oleyl cetyl alcohol 30/70 is considered an effective ingredient for soothing and healing dry skin. Oleyl cetyl alcohol 30/70 is a extremely common multitasker ingredient that gives your skin a nice soft feel (emollient) and Oleyl cetyl alcohol 30/70 gives body to creams and lotions. Oleyl cetyl alcohol 30/70 also helps to stabilize oil-water mixes (emulsions), though Oleyl cetyl alcohol 30/70 does not function as an emulsifier in itself. Oleyl cetyl alcohol 30/70 typical use level in most cream type formulas is 2-3%. Oleyl cetyl alcohol 30/70 (CH3 (CH2) nOH) is a mixture of cetyl and stearyl alcohols from vegetable or synthetic sources. Oleyl cetyl alcohol 30/70 It is classified as a fatty alcohol. Oleyl cetyl alcohol 30/70 is a white, waxy solid substance in the form of flakes. Oleyl cetyl alcohol 30/70 Fat soluble, Oleyl cetyl alcohol 30/70 but not water soluble. Oleyl cetyl alcohol 30/70 In the pharmaceutical and cosmetic industry, Oleyl cetyl alcohol 30/70 acts as an emulsion stabilizer; Oleyl cetyl alcohol 30/70 Matting agent; Oleyl cetyl alcohol 30/70 Surfactant - foam booster; and Oleyl cetyl alcohol 30/70 are used as viscosity increasing agents. Oleyl cetyl alcohol 30/70 Usually used in creams and lotions. Oleyl cetyl alcohol 30/70 Its melting point is 122 ° F (50 ° C) and the boiling point of Oleyl cetyl alcohol 30/70 is: 480. 2 ° F (249 ° C). Oleyl cetyl alcohol 30/70 has a slight characteristic odor. Oleyl cetyl alcohol 30/70 is found as white or pale yellow waxy mass or white flakes or granules. Oleyl cetyl alcohol 30/70 Melts when heated, giving a colorless or pale yellow liquid without turbidity or dispersed particles. Oleyl cetyl alcohol 30/70 Practically insoluble in water; Oleyl cetyl alcohol 30/70 is easily soluble in ether; soluble in alcohol and petroleum ether. Oleyl cetyl alcohol 30/70 When melted, it mixes with fixed oils, liquid paraffin and melted lanolin. Oleyl cetyl alcohol 30/70 is a mixture of solid aliphatic alcohols mainly composed of cetyl alcohol and stearyl alcohol. Oleyl cetyl alcohol 30/70 It is obtained by reducing the appropriate fatty acids. Oleyl cetyl alcohol 30/70 British Pharmacopoeia (BP) and the American National Formula (USNF) state that it should not contain less than 90% cetyl + stearyl alcohol and less than 40% stearyl alcohol. Oleyl cetyl alcohol 30/70 is used in cream, ointment and Oleyl cetyl alcohol 30/70 as a hardener and Setostearyl Alcohol (Oleyl cetyl alcohol 30/70, Oleyl cetyl alcohol 30/70 ) as emulsion stabilizer in other topical preparations. Oleyl cetyl alcohol 30/70 It is useful in the preparation of oil / water type emulsions that can remain stable over a wide pH range in combination with hydrophilic emulsifying agents. Also, Oleyl cetyl alcohol 30/70 is used to increase the softening effect of pomades prepared with paraffin. Although Setostearyl Alcohol (Oleyl cetyl alcohol 30/70, Oleyl cetyl alcohol 30/70 ) is a nonirritant substance, hypersensitivity reactions have been reported due to the main components of Oleyl cetyl alcohol 30/70 cetyl and stearyl alcohol. Oleyl cetyl alcohol 30/70 is a mixture of stearic and cetyl alcohols in equal proportions. In nature, Oleyl cetyl alcohol 30/70 this substance is found in the form of solid white granules of Oleyl cetyl alcohol 30/70 with a characteristic odor. The undoubted advantage of cosmetics with Oleyl cetyl alcohol 30/70 is the extremely low probability of any of them. Oleyl cetyl alcohol 30/70 is not the cheapest and most common substance. Considering the rather high cost of Oleyl cetyl alcohol 30/70 cosmetics, Oleyl cetyl alcohol 30/70 is not only possible to make their own preparation, but also highly desirable. Oleyl cetyl alcohol 30/70 is used in the Pharmaceutical and Cosmetic industries. Appearance Oleyl cetyl alcohol 30/70 It is oily, granular and solid. Oleyl cetyl alcohol 30/70 is white in color. Oleyl cetyl alcohol 30/70 has a characteristic odor. Oleyl cetyl alcohol 30/70 Appearance Oily, granular (Paste) and Solid Oleyl cetyl alcohol 30/70 Color White Oleyl cetyl alcohol 30/70 Odor It has a characteristic odor. Oleyl cetyl alcohol 30/70 Danger In case of skin and eye contact, wash with plenty of water and soap. In case of inhalation or swallowing, apply to the nearest health facility. Oleyl cetyl alcohol 30/70 Properties It is a granular, oily solid raw material with a specific light odor. Oleyl cetyl alcohol 30/70 Usage Area Oleyl cetyl alcohol 30/70 Cosmetic product manufacturing and Oleyl cetyl alcohol 30/70 especially in hair cream production, Oleyl cetyl alcohol 30/70 ) The carrier is actively used in the production of hand and face creams or lotions. In addition, Oleyl cetyl alcohol 30/70 finds use in sweat scent products and Oleyl cetyl alcohol 30/70 sun care products. Oleyl cetyl alcohol 30/70 ; Cetylstearyl alcohol; Cetyl / stearyl alcohol Oleyl cetyl alcohol 30/70 CAS number 67762-27-0 Oleyl cetyl alcohol 30/70 Properties Oleyl cetyl alcohol 30/70 Chemical formula CH 3 (CH 2) n-CH 2 -OH; n = variable, typically 14-16 Oleyl cetyl alcohol 30/70 Melting point 48 to 56 ° C (118 to 133 ° F; 321 to 329 K) [1] Oleyl cetyl alcohol 30/70 Unless otherwise stated, data are given for standardized materials (25 ° C [77 ° F] at 100 kPa). Oleyl cetyl alcohol 30/70 Melts when heated, giving a colorless or pale yellow liquid without turbidity or dispersed particles. Oleyl cetyl alcohol 30/70 Practically insoluble in water; Oleyl cetyl alcohol 30/70 is easily soluble in ether; soluble in alcohol and petroleum ether. Oleyl cetyl alcohol 30/70 When melted, it mixes with fixed oils, liquid paraffin and melted lanolin. Oleyl cetyl alcohol 30/70 is a mixture of solid aliphatic alcohols mainly composed of cetyl alcohol and stearyl alcohol. Oleyl cetyl alcohol 30/70 It is obtained by reducing the appropriate fatty acids. Oleyl cetyl alcohol 30/70 British Pharmacopoeia (BP) and the American National Formula (USNF) state that it should not contain less than 90% cetyl + stearyl alcohol and less than 40% stearyl alcohol. Oleyl cetyl alcohol 30/70 is used in cream, ointment and Oleyl cetyl alcohol 30/70 as a hardener and Setostearyl Alcohol (Oleyl cetyl alcohol 30/70, Oleyl cetyl alcohol 30/70 ) as emulsion stabilizer in other topical preparations. Oleyl cetyl alcohol 30/70 It is useful in the preparation of oil / water type emulsions that can remain stable over a wide pH range in combination with hydrophilic emulsifying agents. Also, Oleyl cetyl alcohol 30/70 is used to increase the softening effect of pomades prepared with paraffin. Although Setostearyl Alcohol (Oleyl cetyl alcohol 30/70, Oleyl cetyl alcohol 30/70 ) is a nonirritant substance, hypersensitivity reactions have been reported due to the main components of Oleyl cetyl alcohol 30/70 cetyl and stearyl alcohol. Oleyl cetyl alcohol 30/70 is a mixture of stearic and cetyl alcohols in equal proportions. In nature, Oleyl cetyl alcohol 30/70 this substance is found in the form of solid white granules of Oleyl cetyl alcohol 30/70 with a characteristic odor. The undoubted advantage of cosmetics with Oleyl cetyl alcohol 30/70 is the extremely low probability of any of them. Oleyl cetyl alcohol 30/70 is not the cheapest and most common substance. Considering the rather high cost of Oleyl cetyl alcohol 30/70 cosmetics, Oleyl cetyl alcohol 30/70 is not only possible to make their own preparation, but also highly desirable. Oleyl cetyl alcohol 30/70 is used in the Pharmaceutical and Cosmetic industries. Oleyl cetyl alcohol 30/70 (CH3 (CH2) nOH) is a mixture of cetyl and stearyl alcohols that can come from vegetable or synthetic sources. It is classified as a fatty alcohol. Oleyl cetyl alcohol 30/70 is a flake-shaped white, waxy, solid material. It is oil soluble but not water soluble. In the pharmaceutical and cosmetic industry, Oleyl cetyl alcohol 30/70 acts as an emulsion stabilizer; opacifying agent; surfactant - foam booster; and viscosity enhancing agent. It is generally used in creams and lotions. It has a melting point of 50 ° C and a boiling point: 249 ° C. Oleyl cetyl alcohol 30/70 . Oleyl cetyl alcohol 30/70 (CH3 (CH2) nOH) is a mixture of cetyl and stearyl alcohols from vegetable or synthetic sources. Oleyl cetyl alcohol 30/70 It is classified as a fatty alcohol. Oleyl cetyl alcohol 30/70 is a white, waxy solid substance in the form of flakes. Oleyl cetyl alcohol 30/70 Fat soluble, Oleyl cetyl alcohol 30/70 but not water soluble. Oleyl cetyl alcohol 30/70 In the pharmaceutical and cosmetic industry, Oleyl cetyl alcohol 30/70 acts as an emulsion stabilizer. Oleyl cetyl alcohol 30/70 is useful in the preparation of oil / water type emulsions that can remain stable over a wide pH range in combination with hydrophilic emulsifying agents. Also, Oleyl cetyl alcohol 30/70 is used to increase the softening effect of pomades prepared with paraffin. Although Setostearyl Alcohol (Oleyl cetyl alcohol 30/70, Oleyl cetyl alcohol 30/70 ) is a nonirritant substance, hypersensitivity reactions have been reported due to the main components of Oleyl cetyl alcohol 30/70 cetyl and stearyl alcohol. Oleyl cetyl alcohol 30/70 is a mixture of naturally derived (Coconut and Palm Oil) fatty alcohols, mainly Cetyl and Stearyl Alcohol. Oleyl cetyl alcohol 30/70 develops a very effective viscosity in your creams, lotions and other personal care products, including anhydrous formulations such as body brighteners or oil blends. This amazing ingredient can be used to change the rheology and viscosity in the creation of both O / W and W / O emulsions. In addition to the improved viscosity, Oleyl cetyl alcohol 30/70 also gives the formulation its emollience. Compared to Cetyl Alcohol, Setostearyl alcohol offers increased viscosity building effects as well as increased penetration of other additives. Oleyl cetyl alcohol 30/70 has long been known as "carrier" and "penetration enhancer". Oleyl cetyl alcohol 30/70 is a mixture of solid aliphatic alcohols mainly composed of cetyl alcohol and stearyl alcohol. Oleyl cetyl alcohol 30/70 It is obtained by reducing the appropriate fatty acids. Oleyl cetyl alcohol 30/70 British Pharmacopoeia (BP) and the American National Formula (USNF) state that it should not contain less than 90% cetyl + stearyl alcohol and less than 40% stearyl alcohol. Oleyl cetyl alcohol 30/70 is used in cream, ointment and Oleyl cetyl alcohol 30/70 as a hardener and Setostearyl Alcohol (Oleyl cetyl alcohol 30/70, Oleyl cetyl alcohol 30/70 ) as emulsion stabilizer in other topical preparations. Oleyl cetyl alcohol 30/70 It is useful in the preparation of oil / water type emulsions that can remain stable over a wide pH range in combination with hydrophilic emulsifying agents. Also, Oleyl cetyl alcohol 30/70 is used to increase the softening effect of pomades prepared with paraffin. Although Setostearyl Alcohol (Oleyl cetyl alcohol 30/70, Oleyl cetyl alcohol 30/70 ) is a nonirritant substance, hypersensitivity reactions have been reported due to the main components of Oleyl cetyl alcohol 30/70 cetyl and stearyl alcohol. Oleyl cetyl alcohol 30/70 is a mixture of stearic and cetyl alcohols in equal proportions. In nature, Oleyl cetyl alcohol 30/70 is found in the form of solid white granules with a characteristic odor. It is used as a conditioning agent because it moisturizes enough and improves the wet / dry combout. A 30/70 blend will form a harder emulsion than Oleyl cetyl alcohol 30/70 70/30. Oleyl cetyl alcohol 30/70 is a mixture of fatty alcohols mainly composed of cetyl alcohol and stearyl alcohol. These alcohols generally conform to the following formula. Cetyl Alcohol Empirical Formula C16H34O or CH3 (CH2) 14CH2OH Stearyl Alcohol Empirical Formula C18H38O or CH3 (CH2) 16CH2OH Oleyl cetyl alcohol 30/70 Practically insoluble in water; Oleyl cetyl alcohol 30/70 is easily soluble in ether; soluble in alcohol and petroleum ether. Oleyl cetyl alcohol 30/70 When melted, it mixes with fixed oils, liquid paraffin and melted lanolin. Oleyl cetyl alcohol 30/70 : Used as emulsifier and thickener in lotions Oleyl cetyl alcohol 30/70 : oils derived from coconut and palm. this is not a drying alcohol. Used as an emollient and to protect skin against moisture loss. A gentle moisturizer, sweat booster, and emulsifier. In hair products, it is used to smooth and soften hair cuticle. Oleyl cetyl alcohol 30/70 -A secondary emulsifier that thickens or adds body to lotions. Oleyl cetyl alcohol 30/70 derived from vegetable extracts and a natural thickener, emulsifier. Common types of alcohol you may encounter in hair care products are lauryl alcohol, cetyl alcohol, myristyl alcohol, Oleyl cetyl alcohol 30/70 , stearyl alcohol and behenyl alcohol. Oleyl cetyl alcohol 30/70 , Oleyl cetyl alcohol 30/70 , or cetylstearyl alcohol is a mixture of fatty alcohol consisting predominantly of cetyl and stearyl alcohols and classified as an alcohol alcohol. Oleyl cetyl alcohol 30/70 When to tighten or add as a styptic. Oleyl cetyl alcohol 30/70 They are used to dissolve and mix the components in it. Oleyl cetyl alcohol 30/70 They are used to lighten the skin. Oleyl cetyl alcohol 30/70 Emulsifier from vegetable raw materials. Oleyl cetyl alcohol 30/70 Add to emulsions to prevent the ingredients in cosmetic formula from splitting Oleyl cetyl alcohol 30/70 Viscosity corrector (regulator) and stabilizer of lotions and creams of M / In emulsions Oleyl cetyl alcohol 30/70 Primary structural surfactant deodorant / antiperspirant is used in solid structures. Oleyl cetyl alcohol 30/70 Does not have irritative activity, Oleyl cetyl alcohol 30/70 promotes the penetration of nutrients into the deeper layers of the skin. Oleyl cetyl alcohol 30/70 Creates a moisture retention film and has a disinfecting effect. Oleyl cetyl alcohol 30/70 gives the skin a soft pleasant feeling. Oleyl cetyl alcohol 30/70 Promotes binding and discounting in creams, lipsticks and other cosmetic products in large amounts of water. Oleyl cetyl alcohol 30/70 Emulsion softener and stabilizer. Oleyl cetyl alcohol 30/70 Conditioner for hair improves its structure and facilitates combing. Cetearyl stearyl alcohol for use as an emulsifier, softener, viscosity controller or dispersant. It can also be used as a chemical intermediate in products such as deodorants and cleaners, where it improves its foaming properties. As a result, you'll find cetyl alcohol and stearyl alcohol in a wide variety of personal care products, lubricants, resins, cosmetics, and more. Lions, creams, hair shampoos, creams, body washes, makeup products. Oleyl cetyl alcohol 30/70 Ethoxylate (C16-18 Alcohol ethoxylate) also Ceteareth, alpha-Ceto Stearyl l-omega-hydroxy-poly (oxy-1,2-ethanediyl), CETEARYL STEARYL Alcohol Ethoxylated, Polyoxyethylene Ceto Stearyl Alcohol, Polyethylene Glycol Ceto Stearyl Ether. Oleyl cetyl alcohol 30/70 Ethoxylate is white, waxy and solid / scale based on ethoxylation. More than 10 molecules of ethoxylate are soluble in water and also soluble in polar solvents. They are non-ionic, biodegradable surfactants. Oleyl cetyl alcohol 30/70 Ethoxylate is widely used in various industrial applications in the fields of textile, medicine, chemistry and agriculture. Oleyl cetyl alcohol 30/70 Ethoxylate is white, waxy and solid / scale based on ethoxylation. More than 10 molecules of ethoxylate are soluble in water and also soluble in polar solvents. They are non-ionic, biodegradable surfactants. Oleyl cetyl alcohol 30/70 Ethoxylate is widely used in various industrial applications in the fields of textile, medicine, chemistry and agriculture. Skin Care: All Creams, Lotions Hair Care: Conditioners, Cream Rinse, Styling Aids Body Care: Creams, Lotions, Salves and Anhydrous Products Use Oleyl cetyl alcohol 30/70 in Cosmetics: We recommend that you dissolve Oleyl cetyl alcohol 30/70 with the oily phase. Additional operating conditions refer to general principles for uptake of M / In emulsionsOleyl cetyl alcohol 30/70 is usually applied in creams and hair balms. Oleyl cetyl alcohol 30/70 Active ingredients in antimicrobial preparations. Oleyl cetyl alcohol 30/70 Thickener for Shampoos Oleyl cetyl alcohol 30/70 Emulsifiers for creams, hair masks Cetyl stearyl alcohol 30-70 Used in cream, lotion, ointment, shampoo, conditioner, balm, make-up products. Oleyl cetyl alcohol 30/70 A common multitasker ingredient in body creams and lotions that gives your skin a pleasant and soft feeling (emollient). Oleyl cetyl alcohol 30/70 It also helps to balance oil-water mixtures. Oleyl cetyl alcohol 30/70 Fatty alcohols have oil-soluble (and therefore softening) tail pieces, and Oleyl cetyl alcohol 30/70 which makes them completely dry and not irritating and Oleyl cetyl alcohol 30/70 makes it completely suitable for the skin. Oleyl cetyl alcohol 30/70 Emulsifier from vegetable raw materials. Oleyl cetyl alcohol 30/70 Add to emulsions to prevent the ingredients in cosmetic formula from splittingOleyl cetyl alcohol 30/70 Viscosity corrector (regulator) and stabilizer of lotions and creams of M / In emulsionsOleyl cetyl alcohol 30/70 Primary structural surfactant deodorant / antiperspirant is used in solid structures. Oleyl cetyl alcohol 30/70 Does not have irritative activity,Oleyl cetyl alcohol 30/70 promotes the penetration of nutrients into the deeper layers of the skin. Oleyl cetyl alcohol 30/70 Creates a moisture retention film. Oleyl cetyl alcohol 30/70 has a disinfecting effect. Oleyl cetyl alcohol 30/70 gives the skin a soft pleasant feeling. Oleyl cetyl alcohol 30/70 Promotes binding and discounting in creams, lipsticks and other cosmetic products in large amounts of water. Oleyl cetyl alcohol 30/70 Emulsion softener and stabilizer. Oleyl cetyl alcohol 30/70 strukturoobrazovatel and gentle. Oleyl cetyl alcohol 30/70 Conditioner for hair improves its structure and facilitates combing. Oleyl cetyl alcohol 30/70 is a so-called fatty alcohol, a mix of cetyl and stearyl alcohol, other two emollient fatty alcohols. Though chemically speaking, Oleyl cetyl alcohol 30/70 is alcohol (as in, it has an -OH group in its molecule), properties of Oleyl cetyl alcohol 30/70 are totally different from the properties of low molecular weight or drying alcohols such as denat alcohol. Oleyl cetyl alcohol 30/70 have a long oil-soluble (and thus emollient) tail part that makes them absolutely non-drying and non-irritating and are totally ok for the skin. Oleyl cetyl alcohol 30/70 is a mixture of naturally derived (Coconut and Palm Oil) fatty alcohols consisting predominantly of Oleyl cetyl alcohol 30/70. Cetearyl Alcohol offers very efficient viscosity building in your creams, lotions, and other personal care products, including anhydrous formulations such as body polishes or oil blends. This fabulous ingredient can be utilized to modify rheology and viscosity in the creation of both O/W and W/O emulsions. In addition to enhanced viscosity, Oleyl cetyl alcohol 30/70 also imparts its own emolliency in the formulation. When compared to Cetyl Alcohol, Cetearyl Alchol offers enhanced viscosity building effects as well as improved penetration of other ingredients. Oleyl cetyl alcohol 30/70 has long been known as a carrier and penetration enhancer. Cetyl stearyl alcohol 30-70 is widely used fatty alcohol is often employed as the sole conditioning agent in crme rinse or hair conditioner formulations, as it adequately moisturizes and improves wet/dry combout. The 30/70 blend will create a stiffer emulsion than the Cetearyl Alcohol 70/30 will. If you are looking for a softer emulsion then look at Cetearyl Alcohol 70/30 or Stearyl Alcohol INCI: Oleyl cetyl alcohol 30/70 Claims of Oleyl cetyl alcohol 30/70: Emulsion Stabilizers Opacifying Agents Surfactants - Foam Boosters Viscosity Increasing Agents - Aqueous Viscosity Increasing Agents - Nonaqueous Applications/Recommended for: Skin care (Facial care, Facial cleansing, Body care, Baby care) Decorative cosmetics/Make-up Toiletries (Shower & Bath, Oral care. . . ) Hair care (Shampoos, Conditioners & Styling) Perfumes & fragrances Sun care (Sun protection, After-sun & Self-tanning) Recommended use levels: 0. 5-10. 0%, depending on the application Cetyl stearyl alcohol 30-70 plant derived emulsifier. solid white wax-like product with typical fat-like odour. Fatty alcohols are prepared from fatty acids by esterification and catalytic hydrogenation. fatty alcohols have a wide range of uses as ingredients in lubricants, resins, perfumes and cosmetics. , emollients, emulsifiers and thickeners in ointments of various sorts and are widely used as a hair coating in shampoos and hair conditioners. also used as a consistency-giving factor in cosmetics and personal care creams and lotions. fatty alcohols are emulsifiers and emollients to make skin smoother and prevent moisture loss. Identical fatty esters are used to improve rub-out of formulas and to control viscosity and dispersion characteristics in cosmetics, personal care products and pharmaceutical ingredients. USES PERSONAL CARE - COSMETIC • Oleyl cetyl alcohol 30/70 - an emollient used in cosmetics, hair, nail, and skin care products. • Oleyl cetyl alcohol 30/70 , a fatty alcohol derived from the saponification of suitable vegetable oils and the resulting fatty acids produced. Stabilizes emulsion and regulates consistency. • Oleyl cetyl alcohol 30/70: used as an emulsifier and thickener in lotions. • Oleyl cetyl alcohol 30/70: derived from coconut and palm oils. This is not a drying alcohol. Used as an emollient and to protect skin from moisture loss. Improving the effects in skin feel or hair feel. • a gentle humectant, lather booster, and emulsifier. In hair products, it is used to smooth and soften the hair cuticle. Oleyl cetyl alcohol 30/70 - a secondary emulsifier that thickens or adds body to lotions. • Oleyl cetyl alcohol 30/70 derived from vegetable extracts and is a natural thickener, emulsifier VEGAN STATUS Vegan suitable PALM DERIVATIVES STATUS Palm present (RSPO - Mass balanced, sustainable) Cetearyl Alcohol, also called Cetyl-Stearyl Alcohol, is the principal raw material used to synthesize cationic, anionic and nonionic surfactant. It also finds wide application in various industries such as plastics, textiles, medicines, food, farming, machinery, commodity chemicals, and mineral floatation. Oleyl cetyl alcohol 30/70 is a mixture of fatty alcohols consisting predominantly of cetylalcohol and stearyl alcohol. These alcohols conform generally to the formula: Cetyl Alcohol Empirical Formula C16H34O or CH3(CH2)14CH2OH Stearyl Alcohol Empirical Formula C18H38O or CH3(CH2)16CH2OH Vegetable source fatty alcohol derived from sustainable palm and coconut oil fatty alcohols (cetyl and stearyl alcohol) used to thicken and stabilize formulations. Oleyl cetyl alcohol 30/70 imparts an emollient feel to the skin. Oleyl cetyl alcohol 30/70 can be used in water-in-oil emulsions, oil-in-water emulsions, and anhydrous formulations--cream, lotion, ointment, body butter, salt scrubs. Oleyl cetyl alcohol 30/70 (Cetearyl) is a blend of cetyl and stearyl fatty alcohols, and is used as to add viscosity and and as a stabiliser in creams and lotions. Oleyl cetyl alcohol 30/70 is also used as a co-emulsifier and imparts emollient feel and lubricity to the skin. Oleyl cetyl alcohol 30/70 is suitable for us in Creams, Lotions, Balms, Body Butters, Anhydrous Scrubs and Solid Conditioning Bars. Oleyl cetyl alcohol 30/70 is highly compatible with Conditioning Emulsifier and Veg-Emulse, but can be used with all our emuslifiers. - Add for tightening of time or as styptic. - Are used for dissolution and mixing of ingredients among themselves. - Are used for mitigation of skin. - So-Emulgator from vegetable raw materials. - Add to emulsions to prevent division of components in cosmetic formula - correction (regulator) of viscosity and the stabilizer of creams and lotions of emulsions of M / In - as primary structural surfactant is used in firm structures of deodorants/antiperspirants. - Does not render irritant action, - promotes penetration of nutrients into deeper layers of skin. - Forms moisture-holding film, - possesses disinfecting action. - gives soft pleasant feeling to skin - Promotes binding and deduction in creams, lipstick and other cosmetics of large amount of water. - Softener and stabilizer of emulsions. - strukturoobrazovatel and emolent. - the konditsoner for hair, improves their structure, facilitates combing APPLICATIONS OF Cetyl stearyl alcohol 30-70 Oleyl cetyl alcohol 30/70 for use as an emulsifier, emollient, viscosity controller or dispersant. It can also be used as a chemical intermediate in products such as deodorants and cleaners, in which it improves foaming properties. As a result, you can find cetyl alcohol and stearyl alcohol in a wide range of personal care products, lubricants, resins, cosmetics and more. Lotions, creams, hair shampoos, conditioners, body washes, makeup products. Cetostearyl Alcohol Ethoxylate (C16-18 Alcohol ethoxylate) is also known as Ceteareth, alpha-Ceto Stearyl l-omega-hydroxy-poly (oxy-1,2-ethanediyl), Ceto Stearyl Alcohol Ethoxylated, Polyoxyethylene Ceto Stearyl Alcohol, Polyethylene Glycol Ceto Stearyl Ether. Cetostearyl Alcohol Ethoxylate is white, waxy and solid/flake based on the ethoxylation. More than 10 mole ethoxylate is water soluble and also can dissolve in polar solvents. It is biodegradable surfactants with non-ionic property. Cetostearyl Alcohol Ethoxylate is widely used in various industrial applications in textile, pharmaceutical, chemical and agriculture field. These surfactants are used as wetting agents, emulsifiers, room cleaning solutions, metalworking and leather processing factories. Skin Care: All Creams, Lotions Hair Care: Conditioners, Cream Rinse, Styling Aids Body Care: Creams, Lotions, Salves and Anhydrous Products Use in cosmetics: - we recommend to melt cetearyl alcohol together with oil phase. - additional working conditions refer to the general principles of receiving emulsions of M / In -Cetyl stearyl alcohol 30-70 is applied generally in creams and hair balms. - Active ingredients in antimicrobic preparations. - thickener for shampoos - with - emulsifier for creams, masks for hair - Joins in cosmetic creams, deodorants, depilators, eyelash oils, hairsprays, masks for hair.
OLEYL ERUCATE
OLEYL LACTATE N° CAS : 42175-36-0 Nom INCI : OLEYL LACTATE Nom chimique : Propanoic acid, 2-hydroxy-, 9-octadecenyl ester Ses fonctions (INCI) Emollient : Adoucit et assouplit la peau
OLEYL LACTATE
cas no 110-25-8 N-Oleoylsarcosine; 2-(N-Methyloleamido)acetic acid; Oleoylsarcosine; Oleic sarcosine; (Z)-N-Methyl-N-(1-oxo-9-octadecenyl)glycine; Oleyl methylaminoethanoic acid; Oleoyl N-methylaminoacetic acid; Medialanic acid (VAN);
OLEYL SARCOSINE
C16 - C18 Triglycerides; Olus Oil & Vegetable Oil cas no: 68956-68-3
OLEYLAMINE 2 EO
Composition: Oleylamine 2 EO Acid thickener Oleylamine 2 EO is used for thickening hydrochloric acid cleaner compositions Oleylamine 2 EO is a nonionic surfactant providing wetting, foam, emulsification and corrosion inhibition and functions primarily as an acid thickener. Oleylamine 2 EO finds application in cleaners used on vertical surfaces such as toilet bowls, dairy, brewery and food processing equipment. Oleylamine 2 EO is used as a viscosifier in acidic medium and cleansers Acid Thickener Our product range includes a wide range of acid thickener and oleyl amine ethoxylate. By keeping track with the latest market development, we introduce high quality 2-2.5 % Dosage Acid Thickener for HCL that gives long term viscosity stability. The offered thickener is processed using optimum quality chemical compounds and cutting edge technology in line with industry standards. Our provided thickener is tested on different parameters so as to deliver qualitative product at clients’ end. Moreover, clients can avail this thickener from us at nominal prices. Features: Longer shelf life Accurately processed High purity Description ATAMAN CHEMICALS offers acid thickener especially used in the manufacturing of toilet cleaners . Oleylamine 2 EO very effectively thickens hydrochloric acid at a very low dosage of 2% - 2.5%. Oleylamine 2 EO also gives long term viscocity and provides 90% corrosion inhibition in HCl Acid . General Characterstics :- Appearance @ 25 Deg C Yellow to Brownish Viscous Liquid Chemical Description - Ethoxylated Amines Moisture - 1% Max Active Content - 99% Min Density - 0.90 Approx Special Features Easy Dispersion in aqueous systems. Works at very low dosage of 1.8% to 2.5 %. Gives very good consistency in Toilet Cleaner. Very easy to make . Excellent thickness of Toilet Cleaner Formed. Instructions for Use Hydrochloric Acid ( HCl ) should be of 33% Purity Min and should be Iron Free. HCl Acid should not be very dark yellow in colour. Wear Safety Masks and Gloves during manufacturing of Toilet Cleaner. Use only Acid Stable colours , for example use Acid Blue for blue color. Procedure for Use: (For Making 100 kg Toilet Cleaner Batch) First take 68 Kg Water in the reactor. Now add 2 kg Oleylamine 2 EO in the water and stirr well for 10 minutes. Now while stirring continuously , add 30 kg HCL of atleast 33% Purity. Continue stirring for 10 minutes so that acid thickener gets mixed completely in the solution. Now you can add any acid stable colour as per your choice . You can adjust dosage of Oleylamine 2 EO as per the thickness required. Storage and Handling: The product can be stored at ambient temperature for two years. Product properties *) Active substance content: about 100 % Appearance at 25 °C: yellowish to brownish liquid pH (DIN EN 1262), 1 % aqueous solution, 20 °C: 9 – 11 Solubility at 20 °C 1 % in water: turbid 10 % in mineral oil: clear 10 % in xylene: clear 10 % in glycol: turbid Density (DIN 51757) at 50 °C: 0.89 g/cm³ Viscosity (DIN 53015) at 50 °C :approx. 35 mPas Refractive index (DIN 53491) at 50 °C: approx. 1.463 Pour point (DIN/ISO 3016): approx. 15 °C Flash point (DIN/ISO 2592): > 200 °C Alkaline number (mg KOH/1 g amine): 156 - 164 Remarks: Product must be homogenized at 30 – 40 °C before use. POE OLEYL AMINE ETHOXYLATE Oleylamine with 2 mol EO is used as thickener for HCl and Phosphoric acid based systems. Oleylamine 2 EO is a compound of non-ionic surfactant and cationic surfactant, which is used in thickening of strong acidic systems, such as toilet cleaner and rust remover Characteristics 1. Excellent thickening effect on strong acid system 2. Small amount added, stable system after thickening 3. Simple use, add at room temperature, can obtain good thickening effect Dosage: 1% - 2.5% Production Process: 1. Add water into the pot first, and slowly add NP 10 (solubilizing essence, making the system more transparent and stable) after stirring, and add pigment after fully dissolved. 2. Slowly add thickener Oleylamine 2 EO under high-speed stirring, and the thickener will disperse into milky liquid in water. 3.Add hydrochloric acid, stir, the liquid slowly thicken and become transparent. 4. Add essence and stir until the product is transparent Note: NP 10 surfactant has been added to the thickener to improve the detergent's decontamination and spreadability. The product has a certain amount of foam to remove the greasy substances in the urine scale ACID THICKENER Acid thickener thickens and increases the viscosity of a range of acid systems including phosphoric, sulfuric, hydrofluoric, citric, oxalic etc. It is a multifunctional material featuring effective thickening, wetting, corrosion inhibition and perfume solubilization. It is especially used in compositions such as toilet bowl cleaners, metal cleaners and brighteners, rust stain removers, denture cleansers, metal descalers, general hard surface cleaners, detergent, disinfectants and other cleaning agents. Slightly combining a strong ionic salt such as sodium chloride with an acid thickener provides an adequate composition viscosity in the preferred concentration range of thickening agent as well as increases viscosity in many cases. ATAMAN CHEMICALS offers a fast acting and reliable acid thickener with exceptional thickening properties. AREAS OF APPLICATIONS Acid bowl cleaners Acid truck cleaners Acidic household cleaners Acidic abrasive cleaners Acid rinse aids Acid metal cleaner Building restoration cleaners Fabric softeners Scale and rust removers Detergent sanitizers Cationic silicone emulsions Peroxide based detergents Hydrogen peroxide bleach products Dye levelling aids Rheological uses Cosmetics Breweries and food processing equipments Other vertical surface cleaners PRODUCT FEATURES Non-toxic Non-irritating High solubility Clear liquid Highly compatible with quaternary biocides Biodegradable Long term stable viscosity Ability to thicken both inorganic and organic acids Better replacement of nonionics used for wetting and perfume solubilization Additional corrosion inhibition Thickens both inorganic and organic acids Easy to solubilize Fatty amine ethyloxylates Surface-active fatty amine ethoxylates are obtained by the action of ethylene oxide on fatty amine. The reaction can be represented in summary simplified form by the following general equation: Fatty amine Ethylene oxide Fatty amine ethoxylate x + y = n number of molecules of ethylene oxide added When ethylene oxide is added to the fatty amines, dihydric alcohols with terminal hydroxyl groups are produced. Under suitable conditions further reactions with these are possible. Moreover, the nitrogen can be quaternized. Fatty amine ethoxylates are in principle basic in nature, they form salts with acids and have an alkaline reaction in aqueous solution. In view of their surface activity they must therefore be classified with the cationic compounds and, like them, they have affinity to fibres and surfaces. Nevertheless, they often behave like nonionic surfactants towards many indicators and also in other applications, and all the more so the longer the added ethylene oxide chain is. Their physical and chemical properties, and especially the surface-active ones, are determined largely by the ratio of the hydrophobic fatty amine radical to the hydrophilic solubilizing polyglycol chains in the molecule. The length of the polyglycol chains is indicated by the number of molecules of ethylene oxide added per molecule of fatty amine and is also known as degree of ethoxylation. Since both the type of initial fatty amine and the amount of ethylene oxide can be chosen arbitrarily, there are two possibilities for modifying the hydrophilic/hydrophobic balance. Both have been employed in producing the Genamin product range. This consists of four groups, each of which is based on a different fatty amine and is distinguished by corresponding code letters: C = Coconut fatty amine saturated C8-C18 fatty amines, predominantly C12-C14 O = Oleylamine predominantly unsaturated C18 fatty amines S = Stearylamine saturated C16-C18 fatty amines T = Tallow fatty amine saturated and unsaturated C16-C18 fatty amines A multistage ethoxylation series is available for each of these amines, and the number of added molecules ofethylene oxide is expressed by an additional suffix, e.g. 080 for 8, 150 for 15 and 250 for 25 moles of ethylene oxide per molecule of fatty amine. The last zero in all suffixes indicates that all grades contain practically 100 % active substance. Common degrees of ethoxylation are Genamin grades with 2, 5, 8, 20 and 25 moles of ethylene oxide. If for special purposes a narrower range is required, this can easily be achieved by formulating corresponding blends of neighbouring products. Sometimes, however, blends of more distant products produce even better effects. The procedure is to use the usual mixing rule and to employ the amine numbers as a basis for calculation. Moreover, when entire production batches are taken, any degrees of ethoxylation can be produced. To obtain completely homogeneous blends, it is preferable to employ temperatures of 50 – 60°C. It is recommended that this temperature should be also maintained when aqueous dilutions are produced. In certain concentration ranges (usually between 70 and 40 % active substance) the occurrence of gelatinous hydrates, which are slow to dissolve in cold water, is avoided. In suitable cases the gel state can be eliminated by adding solubilizers (alcohols, glycols, etc.). These are also appropriate if stable, non-flammable, higher dilutions are to be produced from products that form a turbid solution. In principle the solubility in water rises with increasing degree of ethoxylation. The slightly ethoxylated products are only moderately dispersible at room temperature and therefore form turbid solutions resembling emulsions. The medium and higher-ethoxylated products dissolve to form a clear solution. On the other hand, the solubility in water decreases with rising temperature. Therefore turbidity can occasionally occur even in inherently clear solutions, for example if the recommended working temperature of 50 – 60°C is maintained when dilutions are prepared. This is a reversible physical phenomenon that normally impairs neither further processing nor subsequent use. The solutions become clear again as they cool. Higher-ethoxylated compounds display no turbidity in aqueous solution up to boiling point. However, with these too the temperature limit is depressed to a greater or lesser extent by large quantities of electrolytes, especially neutral salts or alkalis.
Oleylamine 2 EO
9-Octadecenylamine; (Z)-Octadec-9-enylamine; 1-Amino-9-octadecene, (9Z)-Octadecene CAS NO:112-90-3
Oleylamine 2EO
1-Amino-9-octadecene; Oleinamine; 9-octadecenylamine; (Z)-9-Octadecen-1-amine; Oleamine; Oleylamin; 1-AMINO-9-OCTADECENE; CIS-1-AMINO-9-OCTADECENE; CIS-9-OCTADECENYLAMINE; OLEYLAMINE; (z)-9-octadecen-1-amin; (Z)-9-Octadecen-1-amine; (z)-9-octadecenylamin; (z)-octadec-9-enylamine; 9-octadecenylamine(oda); alamine11; armeeno; kemaminep989; noramo; oleamine; oleinamine; oleylamin; oleylamine(9-octadecenylamine,oda); OLEYLAMINE, TECH., 70%; Oleylamine, approximate C18-content 80-90%; 9-Octadecen-1-amine, (9Z)- CAS NO:112-90-3
Olive Oil Refined
SYNONYMS OLIVAE OLEUM;OLIVE OIL;OLIVE OIL, EXTRA VIRGIN;OLIVE OIL, PURE/RIVIERA;OLIVE OIL, REFINED A;OLIVE POMACE OIL;OIL OF OLIVE;sweetoil CAS NO:8001-25-0
Olive Oil Virgin
SYNONYMS OLIVAE OLEUM;OLIVE OIL;OLIVE OIL, EXTRA VIRGIN;OLIVE OIL, PURE/RIVIERA;OLIVE OIL, REFINED A;OLIVE POMACE OIL;OIL OF OLIVE;sweetoil CAS NO:8001-25-0
Olmesartan Medoxomil
SYNONYMS Azor; 4-(1-Hydroxy-1-methylethyl)-2-propyl-1-((2'-(1H-tetrazol-5-yl) (1,1'-biphenyl)-4-yl)methyl)-1H-imidazole5-carboxylic acid (5-methyl-2-oxo-1,3-dioxol-4-yl) methyl ester; 5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl 5-(2- hydroxypropan-2-yl)-2-propyl-3-((4-(2-(2H-tetrazol-5-yl)phenyl)phenyl)methyl)imidazole-4-carboxylate; Benicar; Olmetec; Votum; cas no:144689-63-4; 144689-24-7 (Parent)
OLUS OIL
EINECS 232-313-5 CAS NO:8002-53-7
olus oil (or) canola oil
OLUS OIL; CANOLA OIL; brassica napus l. oil; canbra oil; rapeseed oil; Olus (Vegetable) Oil CAS NO:68956-68-3
Omeprazole
SYNONYMS 5-Methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole, Antra, Losec cas no:73590-58-6
Omeprazole 7.5%, 8.5% Pellets Anti-Ulceratives
SYNONMYS H 168 68;H 168-68;H 16868;Magnesium, Omeprazole;Omeprazole;Omeprazole Magnesium;Omeprazole Sodium;Prilosec;Sodium, Omeprazole CAS NO:73590-58-6
Omeprazole CEP
SYNONYMS 5-Methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole, Antra, Losec cas no:73590-58-6
Omeprazole Mg
SYNONYMS 5-Methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazoleMagnesium Complex cas no:95382-33-5
Omeprazole Sodium
SYNONYMS Losev; Omeprazole; Prilosec;(R,S)-5-Methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl) methyl]sulfinyl]- 1H-benzimidazole monosodium salt; Losec Sodium; Omepral; Andra; Sodium 5-methoxy-2-[(4-methoxy-3,5- dimethyl-pyridin-2-yl)methylsulfinyl]benzoimidazole; cas no:73590-58-6, (Base) 95510-70-6 (Sodium)
OMNIRAD TPO
Omnirad TPO представляет собой высокоэффективный фотоинициатор типа I с низким уровнем пожелтения, используемый для инициирования радикальной полимеризации ненасыщенных олигомеров, например акрилаты после воздействия УФ-света. Омнирад ТПО можно использовать в сочетании с моно- или многофункциональными мономерами в качестве реактивных разбавителей.
Omnirad TPO — это фотоинициатор, используемый во многих отраслях производства красок.

КАС: 75980-60-8
МФ: C22H21O2P
МВт: 348,37
ИНЭКС: 278-355-8

Omnirad TPO представляет собой фотоинициатор на основе моноацилфосфиноксида, который можно включать в различные полимерные матрицы для эффективного отверждения и стабильности цвета смолы.
Omnirad TPO-L может использоваться после соответствующего тестирования в составе отверждаемых УФ-излучением покрытий и красок на основе акрилатов для таких подложек, как бумага, дерево, металл, пластик и стекло.
Для улучшения отверждения поверхности.
Омнирад ТПО-Л обычно комбинируют с другими фотоинициаторами, такими как Омнирад 481, Омнирад 73.
и Omnirad BP Flake.
Свойства готового продукта будут зависеть от фактически используемых реакционноспособных мономеров, олигомеров и добавок.

Омнирад ТПО — эффективный свободнорадикальный (1)-тип, высокоэффективный фотоинициатор с поглощением в длинноволновом диапазоне.
Из-за широкого диапазона поглощения Omnirad TPO эффективный пик поглощения составляет 350 ~ 400 нм, а пик поглощения составляет около 420 нм, что длиннее, чем у обычного инициатора, после того, как свет может генерировать бензоил и фосфорил, два свободных радикала могут инициировать полимеризация, поэтому скорость отверждения света высо��ая, Omnirad TPO также обладает эффектом фотоотбеливания, подходит для толстой пленки Глубокое отверждение и характеристики покрытия без желтого цвета, с низкой летучестью, подходят для водной основе.

Химические свойства Омнирад ТПО
Температура плавления: 88-92 °C (лит.)
Температура кипения: 519,6 ± 60,0 ° C (прогнозировано)
Плотность: 1,12 г/мл при 25 °C (лит.)
Давление пара: 0 Па при 25 ℃
Показатель преломления: n20/D 1,475 (лит.)
Fp: >230 °F
Температура хранения: запечатанный в сухом, комнатная температура
Растворимость: растворим в метаноле
Форма: порошок в кристалл
Цвет: от светло-желтого до желтого и зеленого
Растворимость в воде: 3,4 мг/л при 20℃
λmax: 400 нм (DMF) (лит.)
Стабильность: Стабильная. Несовместим с сильными окислителями.
InChIKey: VFHVQBAGLAREND-UHFFFAOYSA-N
LogP: 3,1 при 23 ℃
Ссылка на базу данных CAS: 75980-60-8 (Ссылка на базу данных CAS)
Система регистрации веществ EPA: Omnirad TPO (75980-60-8)

Использование
Omnirad TPO можно использовать для фотосшивания композита на основе ПММА, который в дальнейшем можно использовать в качестве изолятора затвора в органических тонкопленочных транзисторах (OTFT).
Omnirad TPO также можно использовать для формирования УФ-отверждаемых уретан-акрилатных покрытий.
Омнирад ТПО также может быть использован в фотоиндуцированной реакции образования фосфинорганических соединений, которые потенциально находят применение в качестве лигандов с металлическими катализаторами и реагентами.

Omnirad TPO, используемый для белой системы, может использоваться для УФ-отверждаемого покрытия, печатной краски, УФ-отверждаемого клея, покрытия для оптического волокна, фоторезиста, фотополимерной печатной формы, смолы для стереолитографии, композитного материала, материала для пломбирования зубов и т. д.

Omnirad TPO является фотоинициатором, который в основном используется в красках для трафаретной печати, красках для литографической печати, красках для флексографской печати и покрытиях для дерева.
Omnirad TPO на белой поверхности или на поверхности с высоким содержанием пигмента диоксида титана может быть полностью отвержден.
Широко используется в различных покрытиях из-за его превосходных поглощающих свойств, что делает Omnirad TPO особенно подходящим для красок для шелковой печати, литографии, красок для флексографской печати, покрытий для дерева.
Отсутствие пожелтения покрытия, низкий эффект постполимеризации и отсутствие остатка.
Omnirad TPO также можно использовать для прозрачных покрытий, особенно для продуктов с низкими требованиями к запаху.
При использовании отдельно в ненасыщенных полиэфирах стиролсодержащих систем Omnirad TPO обладает высокой эффективностью инициирования.

Для акрилатной системы, особенно окрашенной системы, обычно необходимо использовать амин или акриламид, в то же время и другое соединение фотоинициатора, чтобы добиться полного отверждения системы, особенно подходит для слабого пожелтения, отверждения белого системы и толстопленочные слои.
Фотоинициатор Omnirad TPO можно использовать в сочетании с PDB 240 или CBP 393 для повышения эффективности отверждения.
Omnirad TPO является лучшим растворителем для экстракции нефтяных ароматических углеводородов, а также используется в качестве реагента для формилирования в тонкой химической промышленности.
Omnirad TPO – лучший растворитель для экстракции нефтяных ароматических углеводородов; Смешанный раствор N-формилморфолина и морфолина (1:1) является экстракционным растворителем для установки по производству метилэтилкетона.

Синонимы
75980-60-8
Дифенил(2,4,6-триметилбензоил)фосфиноксид
(Дифенилфосфорил)(мезитил)метанон
Оксид фосфина, дифенил(2,4,6-триметилбензоил)-
дифенилфосфорил-(2,4,6-триметилфенил)метанон
ИНЭКС 278-355-8
дифенил(2,4,6-триметилбензоил)фосфиноксид
DTXSID4052502
2,4,6-триметилбензоилдифенилфосфиноксид
2,4,6-триметилбензоилдифенилфосфиноксид
УНИ-B9EIM2D97X
B9EIM2D97X
Метанон, (дифенилфосфинил) (2,4,6-триметилфенил)-
дифенил(2,4,6-триметилбензоил)фосфиноксид
триметилбензоилдифенилфосфиноксид
ТПО
ЕС 278-355-8
Фотоотверждение ТПО
2,4,6-триметилбензоилдифенилфосфиноксид
ТМДПО
ди(фенил)фосфорил-(2,4,6-триметилфенил)метанон
ЧИВАКУРЕ ТПО
ДВОЙНОЙ ТПО
АДДИТОЛ ТПО
ГЕНОКЮР ТПО
SCHEMBL27651
КЕМБЛ3561198
DTXCID8031075
VFHVQBAGLAREND-UHFFFAOYSA-
Токс21_303757
MFCD00192110
АКОС015840661
CS-W009334
NCGC00357056-01
AC-10380
AS-14718
КАС-75980-60-8
ЛС-106027
2,4,6-триметилбензоилдифенилфосфиноксид
Д3358
FT-0609902
2,4,6-триметилбензоилдифенилфосфиноксид
2,4,6-триметилбензоил-дифенилфосфиноксид
О11728
(2,4,6-триметилбензоил)дифенилфосфиноксид
дифенил(2,4,6-триметилбензоил)оксид фосфора
дифенил-2,4,6-триметилбензоилфосфиноксид
дифенил(2,4,6-триметилбензоил)фосфиноксид
дифенил-(2,4,6-триметилбензоил)фосфиноксид
2,4,6-ТРИМЕТИЛБЕНЗОИЛДИФЕНИЛФОСФИНОКСИД
Метанона, (дифенилфосфинил) (2,4,6-триметилфенил)-
Дифенил(2,4,6-триметилбензоил)фосфиноксид, 97%
Оксид фосфина, дифенил (2,4,6-триметилбензоил)-
Q27274548
ТРИМЕТИЛБЕНЗОИЛДИФЕНИЛФОСФИНОКСИД [INCI]
(ДИФЕНИЛФОСФИНИЛ)(2,4,6-ТРИМЕТИЛФЕНИЛ)МЕТАНОН
Люцирин ТПО твердый (2,4,6-триметилбензоилдифенилфосфиноксид)
ontan wax (acid, esterified and saponified)
CI 351; 4,4'-Bis(2-sulfonatostyryl)biphenyl Disodium Salt; 2,2′-([1,1′-Biphenyl]-4,4′-diyldi-2,1-ethenediyl)bis-benzenesulfonic acid disodium salt; Tinopal CBS-X, Fluorescent Brightener 351 (FB 351 ) , C.I.351, Fluorescent Brightener CBS-X CAS NO:27344-41-8
OPE WAX (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК)
OPE WAX (Окисленный полиэтиленовый воск) — это тип полиэтиленового воска, прошедший процесс окисления.
OPE WAX (окисленный полиэтиленовый воск) обладает превосходной внутренней и внешней смазкой.


Номер CAS: 68441-17-8
Номер ЕС: 614-498-8
Номер леев: MFCD00084426
Молекулярная формула: C51H102O21Si2.



По, Полиоксиэтилен, Окисленный полиэтилен, Окисленный полиэтилен, Окисленные полиэтиленовые воски, Этен, гомополимер, окисленный, Полиэтилен, окисленный, Окисленный полиэтиленовый воск, Этен, гомополимер, окисленный, Окисленный полиэтиленовый воск, Полиэтилен, оксидиз, Окисленный полиэтиленовый воск, Поли(этилен) окисленный, Полиэтилен, окисленный,



OPE WAX (Окисленный полиэтиленовый воск) получают путем окисления полиэтиленового воска.
Молекулы OPE WAX (окисленный полиэтиленовый воск) имеют полярные группы, такие как карбонильные группы и гидроксильные группы, - свойство, которое увеличивает совместимость с наполнителями, пигментами и полярными смолами.


Смачиваемость и диспергируемость OPE WAX (окисленного полиэтиленового воска) также лучше, чем у полиэтиленового воска.
OPE WAX (окисленный полиэтиленовый воск) представляет собой твердый полимер с низкой адгезией, обладающий хорошей химической и термостабильностью, высокой температурой размягчения, а также хорошим смазочным действием.


Молекулярная цепь OPE WAX (окисленный полиэтиленовый воск) имеет определенные функциональные группы, поэтому его растворимость с полярной смолой значительно улучшена, что превосходит полиэтиленовый воск.
OPE WAX низкой плотности (окисленный полиэтиленовый воск) можно заранее пластифицировать, при этом последующий крутящий момент снижается.


OPE WAX (окисленный полиэтиленовый воск) обладает превосходной внутренней и внешней смазкой.
OPE WAX (окисленный полиэтиленовый воск) может улучшить дисперсность красителя, придать изделиям хороший блеск и повысить эффективность производства.
OPE WAX (Окисленный полиэтиленовый воск) представляет собой водорастворимый и термопластичный неионный линейный макромолекулярный полимер, обладающий свойствами флокуляции,
загущение, медленное высвобождение, смазывание, дисперсия, удержание, удержание воды и т. д., он нетоксичен и не вызывает раздражения.


OPE WAX (Окисленный полиэтиленовый воск) представляет собой низкомолекулярный полиэтилен с гидроксилом и карбоксилом.
OPE WAX (Окисленный полиэтиленовый воск) действует как смазка. Обеспечивает хорошую химическую стойкость.
OPE WAX (окисленный полиэтиленовый воск) обладает хорошей внутренней и внешней смазывающей способностью, поэтому он может достигать лучших смазочных свойств, чем другие смазочные материалы, когда он используется в формуле жестких прозрачных или непрозрачных изделий из ПВХ.


OPE WAX (Окисленный полиэтиленовый воск) — это тип полиэтиленового ��оска, прошедший процесс окисления.
OPE WAX (окисленный полиэтиленовый воск) получается в результате полимеризации газообразного этилена и широко используется в различных отраслях промышленности благодаря своим уникальным свойствам.


OPE WAX (окисленный полиэтиленовый воск) обладает хорошей морозостойкостью, термостойкостью, химической стойкостью и износостойкостью, а также хорошей совместимостью с полиэтиленом, полипропиленом, поливинилацетатом и бутилкаучуком.
OPE WAX (окисленный полиэтиленовый воск) может улучшить текучесть полиэтилена, полипропилена и АБС, а также способность полиметилметакрилата и поликарбоната вынимать из формы.


PE-воск - это неокисленный воск, OPE-воск - это окисленный воск с определенным кислотным числом, молекулярная цепь окисленного воска с определенным количеством карбонила и гидроксила, OPE WAX (окисленный полиэтиленовый воск) - отличный новый полярный воск, поэтому совместимость с наполнители, пигменты, полярные смолы значительно улучшены, смазывающая способность, дисперсия лучше, чем у полиэтиленового воска, а также оба связующих свойства.


OPE WAX (окисленный полиэтиленовый воск) может улучшить текучесть полиэтилена, полипропилена, АБС-пластика и извлечение из формы полиметилметакрилата и поликарбоната.
Для ПВХ и других внешних смазок OPE WAX (окисленный полиэтиленовый воск) обладает более сильным внутренним смазочным эффектом по сравнению с другими внешними смазками.


OPE WAX (Окисленный полиэтиленовый воск) имеет низкую вязкость, высокую температуру размягчения, твердость.
OPE WAX (окисленный полиэтиленовый воск) обладает хорошими специальными характеристиками, такими как нетоксичность, хорошая термическая стабильность, высокая температура и низкая летучесть, отличная дисперсия наполнителей, пигментов, отличная внешняя смазывающая способность и сильная внутренняя смазка.


OPE WAX (окисленный полиэтиленовый воск) также обладает связующим эффектом и может повысить эффективность производства при переработке пластмасс.
Низкая стоимость производства, хорошая совместимость с полиолефиновой смолой, OPE WAX (окисленный полиэтиленовый воск) обладает хорошей влагостойкостью при комнатной температуре, сильной химической стойкостью, отличными электрическими свойствами, может улучшить внешний вид готовой продукции.


OPE WAX (окисленный полиэтиленовый воск) является идеальным продуктом для замены монгольского воска, сычуаньского воска, жидкого парафина, микрокристаллического воска, натурального парафина, полиэтиленового воска и так далее.
OPE WAX (Окисленный полиэтиленовый воск) производство полиэтиленового воска после специальной системы окисления.


OPE WAX (Окисленный полиэтиленовый воск) содержит низкомолекулярный полиэтиленоксид, содержащий гидроксильные и карбоксильные группы.
OPE WAX (Окисленный полиэтиленовый воск) представляет собой белый и слегка желтоватый порошок, обладающий хорошей химической стабильностью, растворимый в ароматических углеводородах.
OPE WAX (Окисленный полиэтиленовый воск) изготавливается из полиэтиленового воска после специального процесса окисления.


Молекулярная цепь имеет определенные функциональные группы, поэтому смешиваемость OPE WAX (окисленного полиэтиленового воска) с полярной смолой значительно улучшена.
Благодаря определенному количеству карбонильных и гидроксильных групп в молекулярной цепи OPE WAX (Окисленный полиэтиленовый воск) значительно улучшается совместимость с наполнителями, пигментами и полярными смолами.


Смачиваемость и диспергируемость в полярной системе лучше, чем у полиэтиленового воска, а OPE WAX (окисленный полиэтиленовый воск) также обладает связывающими свойствами.
OPE WAX (окисленный полиэтиленовый воск) используется в промышленности по переработке пластмасс, внутренняя и внешняя смазка ПВХ относительно сбалансирована.
Смазывающая способность OPE WAX (окисленного полиэтиленового воска), добавленного к жесткой, прозрачной и непрозрачной формуле ПВХ, лучше, чем у других смазок.


Благодаря высокой температуре плавления и низкой вязкости OPE WAX (окисленный полиэтиленовый воск) способствует хорошей текучести смолы, относительно снижает энергопотребление при смешивании смолы, уменьшает адгезию между смолой и формой, легко удаляет пленку, играет роль внутреннего и внешняя смазка, а также обладает хорошими антистатическими свойствами.



ИСПОЛЬЗОВАНИЕ И ПРИМЕНЕНИЕ ОПЕ ВОСК (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
OPE WAX (окисленный полиэтиленовый воск) также широко применяется для изготовления кабелей из полиэтилена или ПВХ, профилей из ПВХ, труб в качестве пластической смазки нового типа.
OPE WAX (Окисленный полиэтиленовый воск) изготавливается из полиэтиленового воска путем специального процесса окисления.
OPE WAX (окисленный полиэтиленовый воск) обладает особыми свойствами, такими как низкая вязкость, высокая температура размягчения и хорошая твердость.


OPE WAX (Окисленный полиэтиленовый воск) — нетоксичный, обладающий хорошей термической стабильностью, низкотемпературной летучестью, превосходной дисперсией наполнителей и пигментов.
OPE WAX (окисленный полиэтиленовый воск) не только обладает превосходной внешней смазывающей способностью, но также обладает сильным внутренним смазочным эффектом, а также обладает эффектом сцепления, что может повысить эффективность производства при обработке пластмасс и снизить производственные затраты.


OPE WAX (Окисленный полиэтиленовый воск) используется в качестве термостабилизатора ПВХ и профиля, трубы, плиты и т. д.
После эмульгирования OPE WAX (окисленный полиэтиленовый воск) используется в бумажной, полиграфической, красильной и швейной промышленности, чернилах на водной основе, креме для обуви на водной основе;


OPE WAX (окисленный полиэтиленовый воск) используется в маточной смеси, маточной смеси наполнителя, модифицированной маточной смеси, функциональной маточной смеси;
OPE WAX (Окисленный полиэтиленовый воск) используется термоплавкий клей, клеи.
OPE WAX (Окисленный полиэтиленовый воск) используется Краска, покрытие, краска для дорожной разметки.


OPE WAX (окисленный полиэтиленовый воск) используется во многих продуктах, таких как ПВХ-компаунд, ПВХ-профиль, ПВХ-трубы, ПВХ-кабельный наполнитель, вспомогательные средства для обработки ТПЭ, термоплавкие клеи и листы ПВХ.
OPE WAX (окисленный полиэтиленовый воск) широко используется в производстве бумаги, покрытий, чернил, текстильной печати и крашения, повседневной химической промышленности и других отраслях промышленности.


OPE WAX (окисленный полиэтиленовый воск), используемый в цветной маточной смеси, изделиях из ПВХ, восковой эмульсии (эмульгировании), модифицированном материале.
OPE WAX (окисленный полиэтиленовый воск) используется в качестве смазочных материалов при переработке пластмасс, используется в области термоплавких материалов для дорожной разметки, действует как диспергатор для маточных смесей, пигментов, технического углерода, может использоваться в качестве добавки для различных типов восков, таких как чистка обуви, воск для пола, автомобильный воск и т. д.


OPE WAX (окисленный полиэтиленовый воск) также можно эмульгировать в воде. Эмульсии используются при отделке текстиля для получения гладкой поверхности, что облегчает дальнейшие этапы производства.
OPE WAX (окисленный полиэтиленовый воск) используется во многих продуктах, таких как ПВХ-компаунд, ПВХ-профиль, ПВХ-трубы, ПВХ-кабельный наполнитель, вспомогательные средства для обработки ТПЭ, термоплавкие клеи и листы ПВХ.


OPE WAX (окисленный полиэтиленовый воск) действует как смазка, агент экономии средств и антиадгезив в процессе экструзии, каландрирования, литья под давлением, формования с раздувом ПЭ, ПП и других пластиков.
OPE WAX (окисленный полиэтиленовый воск) действует как диспергатор для маточных смесей, пигментов, технического углерода, добавки к исходному материалу, наполнителя исходного материала и других пигментов.


OPE WAX (окисленный полиэтиленовый воск) применяется в области термоплавких материалов для дорожной разметки.
OPE WAX (окисленный полиэтиленовый воск) действует как добавка для чистки обуви, воска для полов, автомобильного воска, полировочного воска, фарфора, воска для таблеток, красок, покрытий, кабеля, копировальной бумаги, вощеной бумаги, смягчителя текстиля и т. д.


Добавка для обработки резины, антикоррозионное средство для автомобилей и т. д.
Был разработан метод получения OPE WAX (окисленного полиэтиленового воска), который имеет множество применений, например, при производстве пластмасс, резины, кожи, бумаги, чернил, текстиля и т. д.


Эксперименты по окислению полиэтиленовых восков проводились на пилотной установке.
Реактор представлял собой колонный реактор диаметром 0,27 м и высотой 3 м с конической распределительной тарелкой.
Результаты экспериментов показали, что оптимальными условиями получения окисленных полиэти��еновых восков являются: катализатор КМnО4, температура реакции 141—148°С, время реакции 3—7 ч, скорость воздуха 4—8 м/с.


Этим методом можно получить OPE WAX (окисленный полиэтиленовый воск) с кислотным числом выше 30 мгKOH/г.
OPE WAX (окисленный полиэтиленовый воск) используется в качестве смазочного материала при обработке пластмасс, таких как поливинилхлорид, для предотвращения прилипания пластика к горячим поверхностям в оборудовании, что экономит энергию и улучшает свойства материалов таких продуктов, как трубы и профили из ПВХ.


OPE WAX (окисленный полиэтиленовый воск) также можно эмульгировать в воде.
Восковые эмульсии применяются в качестве отделки тканей для получения более гладкой поверхности, облегчения шитья и повышения устойчивости к образованию ворса и катышков.


Полиэтиленовые воски используются в полиролях, наносимых на обувь, мебель, полы и кузов автомобиля, а также в восковых эмульсиях для защиты поверхности, придания блеска или повышения безопасности за счет повышения сопротивления скольжению.
Добавление восковых эмульсий в покрытие глянцевых журналов защищает поверхность от стирания краски.


На кожуру цитрусовых также можно нанести тонкий слой OPE WAX (окисленный полиэтиленовый воск), чтобы предотвратить ее высыхание и образование синяков.
OPE WAX (окисленный полиэтиленовый воск) в виде профилей ПВХ, труб, пластин, цветной маточной смеси, технологической добавки, дозировка 0,3 ~ 0,5% может улучшить качество поверхности обрабатываемых изделий.


Использование OPE WAX (окисленный полиэтиленовый воск) в качестве смазки для обработки пластиковых изделий может эффективно улучшить извлечение из формы, значительно сократить время очистки формы.
OPE WAX (окисленный полиэтиленовый воск) в основном используется для изделий из ДПК и вспененных материалов, таких как: вспененный профиль из ПВХ ДПК, плита, строительный шаблон из ДПК, вспененный профиль, пенопластовая плита и т. д. жесткие изделия.


OPE WAX (окисленный полиэтиленовый воск) широко используется благодаря своей превосходной морозостойкости, термостойкости, химической стойкости и износостойкости.
При обычном производстве OPE WAX (окисленный полиэтиленовый воск) можно добавлять непосредственно при переработке полиолефинов в качестве добавки, которая увеличивает блеск и технологические свойства продукта.


В качестве смазки OPE WAX (окисленный полиэтиленовый воск) имеет стабильные химические свойства и хорошие электрические свойства.
Полиэтиленовый воск растворяется в полиэтилене, полипропилене, поливинилацетате, этиленпропиленовом каучуке и бутилкаучуке.
OPE WAX (окисленный полиэтиленовый воск) может улучшить текучесть полиэтилена, полипропилена, АБС-пластика и извлечение из формы полиметилметакрилата и поликарбоната.


Полиэтиленовые воски обеспечивают более сильную внутреннюю смазку ПВХ, чем другие внешние смазочные материалы.
OPE WAX (окисленный полиэтиленовый воск) также может использоваться в качестве сырья и вспомогательных материалов для кондиционеров для текстиля, автомобильного воска и кондиционера для кожи.
OPE WAX (окисленный полиэтиленовый воск) может использоваться в качестве диспергатора, смазки, отбеливателя и связующего агента для пигментов или наполнителей, таких как плотная маточная смесь, полипропиленовая маточная смесь, маточная смесь добавок и маточная смесь наполнителя.


OPE WAX (Окисленный полиэтиленовый воск) используется в качестве смазок для обработки резины и пластмасс, средств для удаления пленок и фазовых растворителей.
В рецептурах водных покрытий и чернил OPE WAX (окисленный полиэтиленовый воск) обеспечивает превосходную износостойкость, стойкость к адгезии и устойчивость к царапинам.


В настоящее время OPE WAX (окисленный полиэтиленовый воск) широко используется в пенопластах ПВХ, но в других аспектах он используется реже по причинам цены.
Пенопласт ПВХ является наиболее сложным в производстве изделий из ПВХ, с ним возникает больше всего проблем, и его труднее всего решить.
Пластификация может быть значительно ускорена после добавления оксидов.


-Хорошие эмульгирующие свойства, поскольку при окислении OPE WAX (окисленный полиэтиленовый воск) вводится большое количество кислородсодержащих групп, межфазное натяжение во время эмульгирования снижается, благодаря чему может быть получена стабильная эмульсия OPE WAX (окисленный полиэтиленовый воск). и уменьшили количество эмульгатора, что очень важно для полировки.


-OPE WAX (Окисленный полиэтиленовый воск) хорошо совместим с резиной, пластиком, парафином и другими материалами.
Внутренняя и внешняя смазка ПВХ относительно сбалансирована, добавление OPE WAX (окисленного полиэтиленового воска) в состав жесткого прозрачного ПВХ превосходит другие смазочные материалы.


-Молекулярная цепь OPE WAX (окисленный полиэтиленовый воск) имеет определенное количество карбонильных и гидроксильных групп.
OPE WAX (Окисленный полиэтиленовый воск) — это превосходный новый полярный воск, благодаря которому значительно улучшаются совместимость с наполнителями, пигментами и полярными смолами, а также улучшаются смазывающая способность и диспергируемость.
OPE WAX (Окисленный полиэтиленовый воск) превосходит полиэтиленовый воск, а также обладает связующими свойствами.


-OPE WAX (окисленный полиэтиленовый воск) имеет хорошую совместимость с полиолефиновыми смолами и т. д.
OPE WAX (Окисленный полиэтиленовый воск) обладает хорошей влагостойкостью при нормальной температуре, высокой химической стойкостью, отличными электрическими свойствами, улучшенным внешним видом готовой продукции, низкой вязкостью и высокой температурой размягчения.

Хорошая твердость и другие специальные свойства, нетоксичность, хорошая термическая стабильность, низкая летучесть при высоких температурах, отличная дисперсия наполнителей и пигментов, отличная внешняя смазывающая способность, сильная внутренняя смазка и даже вместе OPE WAX (окисленный полиэтиленовый воск) может улучшить производственная эффективность переработки пластмасс и снижение производственных затрат.


-Окисленный полиэтиленовый воск для изделий из ПВХ
*OPE WAX (окисленный полиэтиленовый воск) можно использовать в качестве смазки для ПВХ и других пластиков.
*OPE WAX (окисленный полиэтиленовый воск) является превосходной внутренней и внешней смазкой.
*OPE WAX (окисленный полиэтиленовый воск) может улучшить смазывающую способность между полимером и металлом.
*OPE WAX (окисленный полиэтиленовый воск) может улучшить дисперсию красителей.
*Дайте продуктам хорошую прозрачность и блеск.
* Лучше повысить эффективность производства


-OPE WAX (окисленный полиэтиленовый воск) обычно используется в производстве жестких изделий из ПВХ благодаря его превосходной совместимости с ПВХ и способности улучшать различные свойства конечного продукта.
Вот несколько способов использования OPE WAX (окисленного полиэтиленового воска) при производстве жестких изделий из ПВХ:

*Смазка:
OPE WAX (окисленный полиэтиленовый воск) действует как смазка, уменьшая трение и улучшая текучесть ПВХ во время обработки.
Это облегчает экструзию или литье под давлением жестких изделий из ПВХ, что приводит к улучшению качества поверхности и стабильности размеров.

* Помощь в обработке:
OPE WAX (окисленный полиэтиленовый воск) может действовать как технологическая добавка, улучшая плавление ПВХ-смол и улучшая прочность расплава материала.
OPE WAX (окисленный полиэтиленовый воск) может привести к повышению производительности и снижению процента брака во время производства.

*Модификация воздействия:
OPE WAX (окисленный полиэтиленовый воск) можно использовать в качестве модификатора ударной вязкости в жестких изделиях из ПВХ, улучшая их прочность и устойчивость к ударам.
OPE WAX (окисленный полиэтиленовый воск) особенно полезен в тех случаях, когда продукт может подвергаться механическим напряжениям или ударам, например, трубы или фитинги.

*Антиблокирующий агент:
OPE WAX (Окисленный полиэтиленовый воск) можно использовать в качестве антиадгезива в пленках ПВХ, предотвращая их слипание во время хранения или транспортировки.
Это улучшает обработку и удобство использования для конечных пользователей.

*Матирующий эффект:
OPE WAX (окисленный полиэтиленовый воск) можно использовать для придания матирующего эффекта покрытиям и краскам из ПВХ, в результате чего получается матовый или сатиновый оттенок.
Это полезно в тех случаях, когда глянцевый внешний вид нежелателен.

*Термическая стабильность:
OPE WAX (окисленный полиэтиленовый воск) демонстрирует хорошую термическую стабильность, что позволяет ему выдерживать высокие температуры без существенного разрушения.
Это свойство делает OPE WAX (окисленный полиэтиленовый воск) подходящим для использования в жестких изделиях из ПВХ, которые могут подвергаться воздействию повышенных температур во время обработки или использования.



ХИМИЧЕСКИЙ СОСТАВ ОПЕ ВОСК (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
Молекулярная цепь OPE WAX (окисленный полиэтиленовый воск) имеет определенные функциональные группы, поэтому растворимость его и полярной смолы может быть значительно улучшена, что лучше, чем у полиэтиленового воска.



ПРЕИМУЩЕСТВА OPE WAX (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
OPE WAX (Окисленный полиэтиленовый воск) изготавливается из полиэтиленового воска путем специального процесса окисления.
OPE WAX (Окисленный полиэтиленовый воск) имеет низкую вязкость, высокую температуру размягчения, хорошую твердость и другие особые свойства.
В системе ПВХ OPE WAX низкой плотности (окисленный полиэтиленовый воск) можно заранее пластифицировать, а последующий крутящий момент снижается.
OPE WAX (окисленный полиэтиленовый воск) обладает превосходной внутренней и внешней смазкой.



В ЧЕМ РАЗНИЦА МЕЖДУ ОПЕ-ВОСКОМ (ОКИСЛЕННЫМ ПОЛИЭТИЛЕНОВЫМ ВОСКОМ) И ПОЛИЭТИЛЕНОВЫМ ВОСКОМ?
OPE WAX (Окисленный полиэтиленовый воск) — блестящие пластиковые вспомогательные средства для внутренней и внешней смазки.
OPE WAX (окисленный полиэтиленовый воск) в основном производится с использованием полиэтиленпарафина, стеарата, сульфата стеариновой кислоты, нагреваемого в реакционном сосуде до температуры 380 °C в течение 6–8 часов.

Разница между OPE WAX (окисленным полиэтиленовым воском) и полиэтиленовым воском заключается в том, что OPE WAX (окисленный полиэтиленовый воск) содержит модифицированный восковой продукт полярного гена, поэтому свойства OPE WAX (окисленный полиэтиленовый воск), такие как долговечность и полировка, улучшаются. намного лучше, чем полиэтиленовый воск.

Химические свойства OPE WAX (окисленный полиэтиленовый воск) более стабильны, чем полиэтиленовый воск, нетоксичны и не вызывают коррозии, что делает OPE WAX (окисленный полиэтиленовый воск) более широко используемым.
OPE WAX (окисленный полиэтиленовый воск) — это универсальный и очень полезный материал, который предлагает множество преимуществ в различных отраслях промышленности.

Одним из ключевых преимуществ OPE WAX (окисленного полиэтиленового воска) являются его превосходные смазочные свойства.
Благодаря низкому коэффициенту трения OPE WAX (окисленный полиэтиленовый воск) может эффективно снижать трение между поверхностями, что приводит к снижению износа оборудования и механизмов.

Эта характеристика делает OPE WAX (окисленный полиэтиленовый воск) идеальной добавкой для промышленного применения, такого как обработка пластмасс, производство резиновых смесей и состав покрытий.
Кроме того, OPE WAX (окисленный полиэтиленовый воск) демонстрирует превосходную диспергируемость, что означает, что его можно легко добавлять в различные среды без комкования и осаждения.

Эта особенность OPE WAX (окисленный полиэтиленовый воск) обеспечивает равномерное распределение по желаемым материалам, улучшая их общие характеристики и стабильность.



ПРЕИМУЩЕСТВА OPE WAX (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
1. OPE WAX (окисленный полиэтиленовый воск) можно использовать в качестве смазки для ПВХ и других пластиков.
2. Отличная внутренняя и внешняя смазка.
3. OPE WAX (окисленный полиэтиленовый воск) может улучшить смазывающую способность между полимером и металлом.
4. OPE WAX (окисленный полиэтиленовый воск) может улучшить дисперсию красителей.
5. Придайте продуктам хорошую прозрачность и блеск.
6. Лучше повысить эффективность производства.



ХИМИЧЕСКАЯ ХАРАКТЕРИСТИКА ОПЕ ВОСК (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
Низкий клей, высокая температура размягчения и хорошая твердость со стабильными химическими характеристиками, хорошей термостабильностью, хорошими дисперсионными характеристиками, отсутствием ядов, отсутствием инея и слизистой оболочки; В качестве идеальной смазки для внутренних и наружных работ OPE WAX (окисленный полиэтиленовый воск) может использоваться вместо жидкого парафина, натурального парафина и т. д.



СВОЙСТВА ОПЕ ВОСК (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
OPE WAX (окисленный полиэтиленовый воск) представляет собой белые частицы, чешуйки или порошок, обладающие хорошим смазочным действием, химической стойкостью и хорошими электрическими характеристиками, растворимые в ароматических углеводородах.



ОСОБЕННОСТИ OPE WAX (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
1. Улучшенная совместимость:
OPE WAX (окисленный полиэтиленовый воск) демонстрирует повышенную совместимость с полярными материалами, такими как поливинилхлорид (ПВХ), полипропилен (ПП) и различными покрытиями.
Такая совместимость способствует лучшему диспергированию и адгезии OPE WAX (окисленного полиэтиленового воска) в этих материалах, что приводит к улучшению характеристик и стабильности.

2. Смазка и сопротивление скольжению:
OPE WAX (окисленный полиэтиленовый воск) обладает превосходными смазочными свойствами, снижает трение и улучшает сопротивление скольжению различных продуктов.
OPE WAX (окисленный полиэтиленовый воск) можно использовать в качестве добавки в покрытиях, чернилах и пластмассах для улучшения свойств поверхности и облегчения обработки.

3. Матирующий эффект:
При использовании в покрытиях и красках OPE WAX (окисленный полиэтиленовый воск) может придавать матирующий эффект, приводя к матовому или сатиновому эффекту.
Это особенно полезно в тех случаях, когда глянцевый внешний вид нежелателен.

4. Улучшенные реологические свойства:
OPE WAX (окисленный полиэтиленовый воск) может изменять реологические свойства составов, такие как вязкость и текучесть.
OPE WAX (окисленный полиэтиленовый воск) может действовать как модификатор реологии, улучшая технологичность и эксплуатационные характеристики различных систем.

5. Термическая стабильность:
OPE WAX (окисленный полиэтиленовый воск) демонстрирует хорошую термическую стабильность, что позволяет ему выдерживать высокие температуры без существенного разрушения.
Это свойство делает OPE WAX (окисленный полиэтиленовый воск) подходящим для применений, требующих термостойкости, таких как термоплавкие клеи и покрытия.

6. Антиблокирующие свойства:
OPE WAX (Окисленный полиэтиленовый воск) можно использовать в качестве антиблокировочного агента в пленках, предотвращая их слипание во время хранения или транспортировки.
Это улучшает обработку и удобство использования для конечных пользователей.



OPE WAX (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК) ОБЛАДАЕТ НЕСКОЛЬКИМИ ПРЕИМУЩЕСТВАМИ, В ТОМ ЧИСЛЕ:
1. Улучшенные свойства поверхности:
OPE WAX (окисленный полиэтиленовый воск), как известно, улучшает поверхностные свойства материалов, такие как устойчивость к царапинам и сопротивление скольжению.
OPE WAX (окисленный полиэтиленовый воск) может придать изделиям гладкую и блестящую поверхность и повысить их долговечность.

2. Повышенная технологичность:
OPE WAX (окисленный полиэтиленовый воск) может улучшить технологические характеристики материалов, облегчая их обращение и обработку.
OPE WAX (окисленный полиэтиленовый воск) может уменьшить трение между поверхностями во время обработки, что приводит к улучшению текучести и сокращению времени обработки.

3. Высокая термическая стабильность:
OPE WAX (Окисленный полиэтиленовый воск) обладает высокой термической стабильностью и выдерживает температуру до 150°C без разложения.
Это делает OPE WAX (окисленный полиэтиленовый воск) подходящим для использования в высокотемпературных применениях, таких как термоплавкие клеи и покрытия.

4. Низкая волатильность:
OPE WAX (окисленный полиэтиленовый воск) имеет низкую летучесть, что означает, что он не испаряется в воздух.
Это делает OPE WAX (окисленный полиэтиленовый воск) подходящим для использования в продуктах, для которых важны низкий запах и выбросы, например, в упаковочных материалах для пищевых продуктов.

5. Совместимость:
OPE WAX (окисленный полиэтиленовый воск) совместим с широким спектром полимеров, включая полиэтилен, полипропилен, полистирол и ПВХ.
Это делает OPE WAX (окисленный полиэтиленовый воск) универсальной добавкой, которую можно использовать в различных областях.



ПРЕИМУЩЕСТВА OPE WAX (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
OPE WAX (окисленный полиэтиленовый воск) — это универсальный и очень выгодный материал, который предлагает множество преимуществ в различных отраслях промышленности.
Одно из ключевых преимуществ OPE WAX (окисленный полиэтиленовый воск) заключается в его исключительных смазочных свойствах.
Благодаря низкому коэффициенту трения OPE WAX (окисленный полиэтиленовый воск) уменьшает трение между поверхностями, обеспечивая плавное движение и уменьшая износ.

Кроме того, OPE WAX (окисленный полиэтиленовый воск) демонстрирует превосходную термостойкость, что делает его идеальным выбором для применений, связанных с высокими температурами.
Устойчивость OPE WAX (окисленный полиэтиленовый воск) к химическим веществам еще больше повышает его полезность в отраслях, где часто встречается воздействие агрессивных веществ.

Еще одним существенным преимуществом является способность OPE WAX (окисленный полиэтиленовый воск) улучшать характеристики текучести материалов во время обработки или производственных процессов, таких как экструзия или литье под давлением.
Это свойство не только помогает получить более точную конечную продукцию, но и повышает эффективность производства за счет минимизации простоев, вызванных засорением или заклиниванием оборудования.

Кроме того, OPE WAX (окисленный полиэтиленовый воск) действует как эффективный диспергатор, обеспечивая лучшее распределение пигментов и наполнителей в таких рецептурах, как краски или покрытия, что приводит к улучшению окраски и общему качеству конечного продукта.



ХАРАКТЕРИСТИКИ ОПЕ ВОСК (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
OPE WAX (окисленный полиэтиленовый воск) хорошо совместим с ПВХ и другими добавками ПВХ.
OPE WAX (окисленный полиэтиленовый воск) подходит для многих условий обработки, он может улучшить плавление, плавление, ударную вязкость и блеск поверхности.
OPE WAX (окисленный полиэтиленовый воск) может широко использоваться в прозрачных листах, гранулах, оконных профилях, плитах и трубах.



ОБЗОР РЫНКА И ОТЧЕТ ОПЕ ВОСК (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
OPE WAX (Окисленный полиэтиленовый воск) — это разновидность полиэтиленового воска, который получают путем окисления низкомолекулярного полиэтилена.
OPE WAX (окисленный полиэтиленовый воск) обычно используется в качестве смазочного материала, диспергатора и вспомогательного средства в различных отраслях промышленности, включая производство пластмасс, покрытий, клеев и резины.

Будущие перспективы рынка OPE WAX (окисленный полиэтиленовый воск) позитивны и многообещающи.
Ожидается, что на рынке OPE WAX (окисленный полиэтиленовый воск) в течение прогнозируемого периода будет наблюдаться устойчивый рост.
Технологические достижения и инновации в производстве OPE WAX (окисленный полиэтиленовый воск), вероятно, будут способствовать росту рынка.

Растущий спрос на OPE WAX (окисленный полиэтиленовый воск) со стороны отраслей конечного использования, таких как упаковка, текстиль и краски, является еще одним важным фактором, способствующим росту рынка.
Текущие перспективы рынка OPE WAX (окисленный полиэтиленовый воск) также благоприятны.

Рынок переживает устойчивый рост благодаря широкому спектру применения OPE WAX (окисленного полиэтиленового воска) в различных отраслях промышленности.
Спрос на OPE WAX (окисленный полиэтиленовый воск) особенно высок в промышленности по производству пластмасс, где он используется в качестве смазки и антиадгезива.

Растущий спрос на пластиковые изделия в различных секторах, включая автомобилестроение, строительство и упаковку, стимулирует рост рынка OPE WAX (окисленный полиэтиленовый воск).
Более того, растущая осведомленность о преимуществах OPE WAX (окисленный полиэтиленовый воск), таких как его низкая температура плавления, отличная дисперсия и улучшенные технологические характеристики, еще больше способствует росту рынка.

Кроме того, на рынке OPE WAX (окисленный полиэтиленовый воск) наблюдается появление новых игроков и расширение существующих производителей, что приводит к усилению конкуренции и инновациям в продукции.
Однако такие проблемы, как колебания цен на сырье и экологические проблемы, связанные с утилизацией OPE WAX (окисленный полиэтиленовый воск), могут в некоторой степени препятствовать росту рынка.

Тем не менее, общий прогноз рынка OPE WAX (окисленный полиэтиленовый воск) остается позитивным, с прогнозируемым среднегодовым темпом роста (CAGR) в % в течение упомянутого прогнозируемого периода.



В ЧЕМ РАЗНИЦА МЕЖДУ ОПЕ-ВОСКОМ (ОКИСЛЕННЫМ ПОЛИЭТИЛЕНОВЫМ ВОСКОМ) И ПОЛИЭТИЛЕНОВЫМ ВОСКОМ?
PE-воск - это неокисленный воск, OPE WAX (окисленный полиэтиленовый воск) - это окисленный воск с определенным кислотным числом, молекулярная цепь окисленного воска с определенным количеством карбонила и гидроксила, окисленный полиэтиленовый воск - отличный новый полярный воск, поэтому совместимость с наполнителями, пигментами, полярными смолами значительно улучшается смазывающая способность, дисперсия лучше, чем у полиэтиленового воска, а также оба связующих свойства.

Полиэтиленовый воск имеет хорошую совместимость с полиэтиленом, полипропиленом, поливинилхлоридом, этиленпропиленовым каучуком и бутилкаучуком.
Он может улучшить текучесть полиэтилена, полипропилена, АБС-пластика и выемку полиметилметакрилата и поликарбоната.
Для ПВХ и других внешних смазок полиэтиленовый воск обладает более сильным внутренним смазочным эффектом по сравнению с другими внешними смазками.



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ОПЕ ВОСК (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
Точка размягчения (°С): 90-110
Плотность (г/см3): 0,94-0,96
Кислотный показатель (мг КОН/г): 12-15
Кислотное число: 10–13 КОН мг/г 13–16 КОН мг/г 4–10 КОН мг/г
Точка размягчения ℃ : 100-105
ВязкостьCPS при 140 ℃ : 200-300
Кислотное число, мг КОН/г: 15-20
Внешний вид: Белый шарик
Внешний вид: белый порошок со светло-желтым оттенком.
Молекулярный вес: 3000-4000



МЕРЫ ПЕРВОЙ ПОМОЩИ ОПЕ ВОСК (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
-Описание мер первой помощи:
*При вдыхании:
При вдыхании выведите пострадавшего на свежий воздух.
*При попадании на кожу:
Смыть большим количеством воды с мылом.
*В случае зрительного контакта:
В качестве меры предосторожности промойте глаза водой.
*При проглатывании:
Никогда не давайте ничего перорально человеку, находящемуся без сознания.
Прополоскать рот водой.
-Указание на необходимость немедленной медицинской помощи и специального лечения:
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ OPE WAX (ОКИСЛЕННОГО ПОЛИЭТИЛЕНОВОГО ВОСКА):
-Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Хранить в подходящих закрытых контейнерах для утилизации.



МЕРЫ ПОЖАРОТУШЕНИЯ ОПЕ ВОСК (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Используйте водяной спрей, спиртостойкую пену, сухие химикаты или углекислый газ.
-Дальнейшая информация:
Данные недоступны



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/ПЕРСОНАЛЬНАЯ ЗАЩИТА OPE WAX (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
-Параметры управления:
--Ингредиенты с параметрами контроля на рабочем месте:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
*Защита глаз/лица:
Используйте средства защиты глаз.
*Защита кожи:
Работайте в перчатках.
Вымойте и высушите руки.
*Защита тела:
Непроницаемая одежда
*Защита органов дыхания:
Защита органов дыхания не требуется.
-Контроль воздействия на окружающую среду:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ОПЕ-ВОСКА (ОКИСЛЕННОГО ПОЛИЭТИЛЕНОВОГО ВОСКА):
-Условия безопасного хранения, включая любые несовместимости:
*Условия хранения:
Хранить в прохладном месте.
Хранить контейнер плотно закрытым в сухом и хорошо проветриваемом месте.
Открытые контейнеры необходимо тщательно закрыть и хранить в вертикальном положении во избежание утечки.



СТАБИЛЬНОСТЬ И РЕАКЦИОННАЯ СПОСОБНОСТЬ OPE WAX (ОКИСЛЕННЫЙ ПОЛИЭТИЛЕНОВЫЙ ВОСК):
-Реактивность:
Данные недоступны
-Химическая стабильность:
Стабилен при рекомендуемых условиях хранения.
-Возможность опасных реакций:
Данные недоступны
-Условия, чтобы избежать:
Данные недоступны

OPTICAL BRIGHTNER CBS-127
OPTICAL BRIGHTENER CBS-127 Optical Brightener CBS-127 is highly effective in polymer substrates such as acrylics, thermoplastic polyurethanes, polyvinylchloride, styrene ehomo and copolymers, polyolefins,and other organic substrates. Main applications of Optical Brightener CBS-127 include synthetic fibers,plastics and plastic rubbers. Additional applications include clear varnish,pigmented varnish,paints,printing inks and synthetic leather. Short Description: High quality whitening Optical Brightener FP-127 for PVC CAS NO 40470-68-6 FLUORESCENT BRIGHTENER FP [Chemical name] FLUORESCENT BRIGHTENER FP [Structure] [Molecular weight]418.5 [Physical properties] Melting Range 216-222℃ Specific Gravity(20℃) 1.23g/cm3 λmax in ultra-violet range 350-355nm Solubility (20℃) %W/W Water <0.01 Acetone <0.1 Dimethylacetamide 1.4 Chloroform 0.4 Ethylacetate <0.1 n-Hexne <0.01 Methanol <0.1 [Molecular weight]418.5 [Physical properties] Melting Range of Optical Brightener CBS-127:216-222℃ Specific Gravity(20℃) of Optical Brightener CBS-127: 1.23g/cm3 λmax of Optical Brightener CBS-127 in ultra-violet range 350-355nm Solubility (20℃) of Optical Brightener CBS-127: %W/W Water of Optical Brightener CBS-127: <0.01 Acetone of Optical Brightener CBS-127:<0.1 Dimethylacetamide of Optical Brightener CBS-127: 1.4 Chloroform of Optical Brightener CBS-127: 0.4 Ethylacetate of Optical Brightener CBS-127: <0.1 n-Hexne of Optical Brightener CBS-127:<0.01 Methanol of Optical Brightener CBS-127: <0.1 Methylene chloride of Optical Brightener CBS-127: 0.1 [Volatility(heating rate 20℃/min) Temperature(℃) of Optical Brightener CBS-127 Weight loss(%) 310 1.0 325 2.0 350 2.0 [Applications of Optical Brightener CBS-127: Optical Brightener CBS-127 is highly effective in polymer substrates such as acrylics, thermoplastic polyurethanes,polyvinylchloride,styrene ehomo and copolymers,polyolefins,and other organicsubstrates. Main applications of Optical Brightener CBS-127 include synthetic fibers,plastics and plastic rubbers. Additional applications include clear varnish,pigmented varnish,paints,printing inks and synthetic leather. [Feature of Optical Brightener CBS-127: Optical Brightener CBS-127 features good resistance to heat, exceptional whitening properties,good light fastness and low volatility. Optical Brightener CBS-127 has a brilliant bluish greenish cast ,features good compatilility in various substrates. Optical Brightener CBS-127 is especially suitable for applications such as films and fibers. [Appearance of Optical Brightener CBS-127: Flow free bright yellowish powder. [Storage of Optical Brightener CBS-127: Keep in cool dry place,keep away from sunlight ,Provided the usual precautions for handing chemicals are observed. Avoided dust formation and ignition sources. [Package of Optical Brightener CBS-127: Paper drum lined with plastics bags,net weight 25KG. [Handling&safety of Optical Brightener CBS-127: FPcan be handled in accordance with the usual rules for industrial chemicals.Avoid dust formation and ignition sources. Dosage of Optical Brightener CBS-127: According the whitening demand to choose the dosage, following suggestion dosage: (1) PVC: Whitening:0.01-0.05% (10-50g/100kg) Transparence of Optical Brightener CBS-127:0.0001-0.001% (0.1-1g/100kg) (2) Polybenzene: Whitening of Optical Brightener CBS-127: 0.001% (1g/100kg) Transparence of Optical Brightener CBS-127:0.0001-0.001% (0.1-1g/100kg) (3) ABS: 0.01-0.05% (10-50g/100kg) Description Optical Brightener CBS-127 is a high stability optical brightener agent with very stable excellent whitening effect. No yellowing and discoloring will occur on the products whitening by this whitening agent even if they are stored for a long time. So it is very popular and very widely used in Plastic especially for soft plastic such as wire, cable, artificial leathers etc. Specification: Name Optical brightener agent CBS-127 Appearance Light yellow powder CAS No. 40470-68-6 Molecular Formula C30H26O2 Purity ≥99% Melting point 216-222℃ Ash ≤0.5% Volatile matter ≤0.3% Use Of CBS-127 It is especially suitable for the whitening of PVC and polystyrene series products, and it can also be used for whitening and brightening of other thermoplastics, coatings, inks, and synthetic fibers. Amount of fluorescent whitening agent CBS-127 added per 100kg polymer (reference dosage): PVC: Whitening: 0.01-0.05% (10-50g) Transparent: 0.0001-0.001% (0.1-1g) PS: Whitening: 0.001% (1g) Transparent: 0.0001-0.001% (0.1-1g) ABS: Whitening: 0.01—0.05%(10g-50g)(It can effectively eliminate the inherent yellow in ABS) Transparent: 0.01—0.05(10g-50g) Other plastic Such as poly(methyl methacrylate), Cellulose carbonate etc., the dosage of cbs-127 can refer to the above formula used in the pvc.
Optical brightener CBS-X
Orange,sweet,extract; OIL, ORANGE; ORANGE PEEL OIL, SWEET; ORANGE OIL; ORANGE OIL AND EXTRACT; ORANGE OIL BRAZIL; ORANGE OIL, CALIFORNIA TYPE; ORANGE OIL COLD-PRESSED, CALIFORNIA CAS NO:8028-48-6
ORANGE OIL
cas no 89-98-5 o-Chlorobenzenecarboxyaldehyde; OCAD;2-Chlorobenzene Carbonal; o-Chloorbenzaldehyde (Dutch); 2-Chloorbenzaldehyde (Dutch); 2-chlorbenzaldehyd (German); o-Chlorobenzaldehyde; 2-clorobenzaldeide (Italian); 2-Clorobenzaldehído (Spanish); 2-Chlorobenzaldéhyde (French);
ORGAL 803 CM
Области применения Orgal 803 CM: модификатор цемента, базовые покрытия EIFS и полы из терраццо.


Тип продукта: Акрилы и акриловые сополимеры
Химический состав: Акриловый полимер.


Orgal 803 CM — акриловый полимер, не содержащий APEO и формальдегида, предназначенный для высокоэффективных покрытий для различных наружных и внутренних работ, покрытий по дереву, морилок.
Orgal 803 CM демонстрирует совместимость с алкидами и прозрачность при нанесении морилок на дерево.


Максимальный срок годности Orgal 803 CM составляет 12 месяцев.
При использовании в покрытиях на водной основе Orgal 803 CM демонстрирует адгезию в мокром и сухом виде, превосходную внешнюю долговечность, стойкость к растрескиванию, мелу и щелочам, сохранение блеска и оттенка, а также отличную реологическую реакцию на модификаторы.



ИСПОЛЬЗОВАНИЕ И ПРИМЕНЕНИЕ ORGAL 803 CM:
Orgal 803 CM используется в качестве модификатора цемента, базовых покрытий EIFS и напольных покрытий из терраццо.
Области применения Orgal 803 CM: модификатор цемента, базовые покрытия EIFS и полы из терраццо.


При использовании в покрытиях на водной основе Orgal 803 CM демонстрирует адгезию в мокром и сухом виде, превосходную внешнюю долговечность, стойкость к растрескиванию, мелу и щелочам, сохранение блеска и оттенка, а также отличную реологическую реакцию на модификаторы.
Orgal 803 CM демонстрирует совместимость с алкидами и прозрачность при нанесении морилок на дерево.


Orgal 803 CM используется в клеях, герметиках, красках и покрытиях.
Области применения Orgal 803 CM: краски для дома, полуглянцевые краски из яичной скорлупы, фасадные краски, глянцевые краски, краски для внутренних работ, краски для кухни и ванной комнаты, морилки для дерева.



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ОРГАЛА 803 СМ:
Название продукта: ОРГАЛ П 803 СМ
Химический состав: переменный ток
Всего твердых веществ (%±1): 47
рН: 9,0-9,0
Вязкость (мПа.с макс): 300
MFFT (°C): 10
Тс (°С): 15



МЕРЫ ПЕРВОЙ ПОМОЩИ ORGAL 803 CM:
-Описание мер первой помощи.
*Общие советы:
Покажите этот паспорт безопасности материала лечащему врачу.
*При вдыхании:
После ингаляции:
Свежий воздух.
*При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промыть кожу с
вода/душ.
*В случае зрительного контакта:
После зрительного контакта:
Промойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.
*При проглатывании:
После глотания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.
-Указание на необходимость немедленной медицинской помощи и специального лечения.
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ ORGAL 803 CM:
-Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Закройте дренажи.
Соберите, свяжите и откачайте пролитую жидкость.
Соблюдайте возможные ограничения по материалам.
Возьмите в сухом виде.
Утилизируйте должным образом.
Очистите пораженное место.



МЕРЫ ПОЖАРОТУШЕНИЯ ORGAL 803 CM:
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Углекислый газ (CO2)
Мыло
Сухой порошок
*Неподходящие средства пожаротушения:
Для этого вещества/смеси не установлены ограничения по огнетушащим веществам.
-Дальнейшая информация:
Не допускайте попадания воды для пожаротушения в поверхностные воды или систему грунтовых вод.



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/ПЕРСОНАЛЬНАЯ ЗАЩИТА ORGAL 803 CM:
-Параметры управления:
--Ингредиенты с параметрами контроля на рабочем месте:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
*Защита глаз/лица:
Используйте средства защиты глаз.
Безопасные очки
*Защита тела:
защитная одежда
*Защита органов дыхания:
Рекомендуемый тип фильтра: Фильтр A
-Контроль воздействия на окружающую среду:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ORGAL 803 CM:
-Условия безопасного хранения, включая любые несовместимости:
*Условия хранения:
Плотно закрыто.
Сухой.



СТАБИЛЬНОСТЬ И РЕАКЦИОННАЯ СПОСОБНОСТЬ ОРГАЛА 803 СМ:
-Химическая стабильность:
Продукт химически стабилен при стандартных условиях окружающей среды (комнатная температура).
-Возможность опасных реакций:
Данные недоступны


ORGAL F 4050
ORGAL F 4050 - это сополимер акрила, не содержащий APEO, который предназначен для твердых, устойчивых к царапинам и химическим веществам покрытий мебели и внутренней древесины.
ORGAL F 4050 от Organik Kimya — это сополимер акрила, не содержащий APEO.
ORGAL F 4050 отличается высокой прочностью, высоким блеском и ударной вязкостью.

Номер CAS: 105-59-9
Номер EINECS: 203-312-7

Синонимы: транс-2-гексен, 4050-45-7, (Э)-2-гексен, 2-гексен, (Е)-, 2-гексен, (2Е)-гекс-2-ен, 2Е-гексен, (2Е)-2-гексен, 592-43-8, 2TZ30GGG1A, NSC-74123, Гексен, изомеры, Гексен, изомер, MFCD00009473, транс-Гекс-2-ен, HSDB 5143, 25264-994 3-1, EINECS 246-768-2, UNII-2TZ30GGG1A, UNII-RBV8CN16R2, EINECS 209-755-2, EINECS 223-752-3, NSC 74123, UNII-092313365W, (2E)-гекс-2-ен, AI3-28402, 2-гексен, цис + транс, транс-2-гексен, 97%, (2E)-2-гексен #, 2-ГЕКСЕН, TRANSRBV8CN16R2, 2-Гексен, (цис и транс), 2-Гексен (смешанный цис и транс), DTXSID90881224, CHEBI:137755, NSC74123, ZINC1699507, LMFA11000035, AKOS015840064, 2-Гексен, цис + транс, тех. 85%, (E)-2-C6H12, H0380, 2-Гексен (цис+транс), технический сорт, 85%, Q27255598, 092313365W, Orgal P 74 S, Orgal Duraflex 84 S, Orgal P 086VR, Orgal P 6830, Orgal PST 5010, Orgal PST 100 E, Orgal PST 100, Orgal PST 50 E, Orgal P 806 S, Orgal P 056V, Orgal K 6459 E, Orgal K 6455 E, Orgal PR 9464, Orgal PR 845 A, ORGAL F 4050, Orgal P 888, Orgal P 878, Orgal P 850 RR, Orgal P 850, Orgal P 838 W, Orgal P 8266, Orgal P 8240, Orgal P 826, Orgal P 808, Orgal P 050G, Orgal P 036V, Orgal P 6820, Orgal P 671, Orgal P 653, Orgal P 600, Orgal P 062 V, Orgal P 526, Orgal P 523 V, Orgal PST 50 A, Orgal P 523 V, Orgal P 526, Orgal P 062V, Orgal P 600, Orgal P 653, Orgal P 671, Orgal P 6820, Orgal P 036V, Orgal P 050G, Orgal P 808, Orgal P 826, Orgal P 8240, Orgal P 8266, Orgal PR 9464, Orgal K 649 EN, Orgal K 6455 E, Orgal K 6459 E, Orgal P 056V, Orgal P 806 S, Orgal PR 667

ORGAL F 4050 обеспечивает отличную шлифовальную способность, хорошую стойкость к засорению и холодной жидкости.
ORGAL F 4050 обеспечивает хорошую прозрачность прозрачных покрытий и отличную прозрачность пленки для влажной/сухой воды.
ORGAL F 4050 предназначен для устойчивой к царапинам мебели и однокомпонентных внутренних деревянных покрытий.

Покрытия на основе ORGAL F 4050 отличаются высокой прочностью и показывают хорошую прозрачность, блеск и ударную вязкость.
Покрытия на основе ORGAL F 4050 обладают отличной стойкостью к воздействию бытовой химии.
Пленки обладают хорошей устойчивостью к воздействию бытовой химии.

ORGAL F 4050 представляет собой сополимер акрила, не содержащий APEO.
ORGAL F 4050 отличается высокой прочностью, высоким блеском и ударной вязкостью.
ORGAL F 4050 подходит для грунтовок для внутренних работ, антибактериальных грунтовок для древесины, грунтовочных грунтовок и грунтовок с устойчивостью к вспышкам и ранней ржавчине на металлических поверхностях.

Максимальный срок хранения ORGAL F 4050 составляет 12 месяцев.
Конкретные свойства и применение ORGAL F 4050 зависят от его рецептуры и предполагаемого использования, которое может быть предоставлено производителем или поставщиком продукта.
ORGAL F 4050 – это линейка полимерных эмульсий на основе акриловой, стирол-акриловой и винилакриловой химии.

ORGAL F 4050 - это акриловый полимер, не содержащий APEO, предназначенный для создания высококачественных грунтовок для блокировки морилок для дерева, стен, потолков и металлических поверхностей.
ORGAL F 4050 может использоваться в составах, содержащих оксид цинка и совместим с различными наполнителями и пигментами.
ORGAL F 4050 демонстрирует отличные пятноблокирующие свойства, адгезию к древесине, устойчивость к мгновенной ржавлению.

Эти продукты соответствуют нормам ЛОС, постепенно отказываясь от формальдегида, аммиака и других запрещенных веществ.
ORGAL F 4050 – это линейка полимерных эмульсий на основе акриловой, стирол-акриловой и винилакриловой химии.
Эти продукты соответствуют нормам ЛОС, постепенно отказываясь от формальдегида, аммиака и других запрещенных веществ.

ORGAL F 4050, также известный как N-метилдиэтаноламин и чаще как MDEA, представляет собой органическое соединение с формулой CH3N(C2H4OH)2.
ORGAL F 4050 представляет собой бесцветную жидкость с запахом аммиака.
Пленки обладают хорошей устойчивостью к воздействию бытовой химии.

ORGAL F 4050 обеспечивает отличную шлифовальную способность, хорошую стойкость к засорению и холодной жидкости.
ORGAL F 4050 обеспечивает хорошую прозрачность прозрачных покрытий и отличную прозрачность пленки для влажной/сухой воды.
ORGAL F 4050 предназначен для устойчивой к царапинам мебели и однокомпонентных внутренних деревянных покрытий.

ORGAL F 4050 предназначен для твердых внутренних покрытий древесины, требующих устойчивости к царапинам и химическим веществам.
Покрытия, изготовленные с помощью ORGAL F 4050, будут обладать хорошей прозрачностью, блеском и ударной вязкостью.
Акриловый сополимер для промышленных покрытий по дереву, мебельных покрытий с повышенной жесткостью, химической стойкостью и стойкостью к истиранию.

Покрытия на основе ORGAL F 4050 обладают повышенной прочностью, твердостью, блеском и прозрачностью.
Формирующая пленка устойчива к воздействию бытовой химии.
ORGAL F 4050 - это сополимер акрила, не содержащий APEO, который предназначен для твердых, устойчивых к царапинам и химическим веществам покрытий мебели и внутренней древесины.

ORGAL F 4050 отличаются высокой прочностью и хорошей прозрачностью, блеском и ударной вязкостью.
Покрытия на основе ORGAL F 4050 обладают отличной стойкостью к воздействию бытовой химии.
ORGAL F 4050 смешивается с водой, этанолом и бензолом.

Третичный амин ORGAL F 4050 широко используется в качестве подсластителя в химической, нефтеперерабатывающей промышленности, производстве синтез-газа и природного газа.
Аналогичными соединениями являются ORGAL F 4050, первичный амин, и диэтаноламин (DEA), вторичный амин, оба из которых также используются для обработки аминных газов.
Определяющей характеристикой ORGAL F 4050 по сравнению с этими другими аминами является его способность преимущественно удалять H2S (и удалять CO2) из потоков высокосернистого газа.

Популярность ORGAL F 4050 в качестве растворителя для очистки газов обусловлена несколькими его преимуществами по сравнению с другими алканоламинами.
Одним из таких преимуществ является низкое давление пара, что позволяет получать высокие аминные композиции без заметных потерь через абсорбер и регенератор.
ORGAL F 4050 также устойчив к термическому и химическому разложению и в значительной степени несмешивается с углеводородами.

ORGAL F 4050 - это обычная базовая нота в парфюмерии, позволяющая аромату сохраняться.
Наконец, ORGAL F 4050 имеет относительно низкую теплоту реакции с сероводородом и углекислым газом, что позволяет снизить нагрузку на ребойлер и, следовательно, снизить эксплуатационные расходы.
ORGAL F 4050 используется в покрытиях для бетонных полов и стен, обеспечивая долговечность и устойчивость к истиранию и химическим веществам.

ORGAL F 4050 используется в производстве PSA для лент, этикеток и наклеек благодаря своим сильным адгезионным свойствам к липкости и отслаиванию.
ORGAL F 4050 используется в рецептурах клеев для строительных материалов, обеспечивая прочное сцепление с такими основаниями, как дерево, металл и пластик.

Внешний вид: Опаловая эмульсия
Содержание твердых веществ (%_1) +: 40
Вязкость (Brookfield LVT 2/60): макс. 500 имп/с
рН: 8,0 - 9,0
MFFT (°C): 49
Стабильность при хранении: Защита от замерзания

ORGAL F 4050 подходит для грунтовок для внутренних работ, антибактериальных грунтовок для древесины, грунтовочных грунтовок и грунтовок с устойчивостью к вспышкам и ранней ржавчине на металлических поверхностях.
ORGAL F 4050 - это акриловый полимер, не содержащий APEO, предназначенный для создания высококачественных грунтовок для блокировки морилок для дерева, стен, потолков и металлических поверхностей.
ORGAL F 4050 может использоваться в составах, содержащих оксид цинка и совместим с различными наполнителями и пигментами.

ORGAL F 4050 демонстрирует отличные пятноблокирующие свойства, адгезию к древесине, устойчивость к мгновенной ржавлению.
Максимальный срок хранения ORGAL F 4050 составляет 12 месяцев.
ORGAL F 4050 менее реактивен по отношению к CO2, но имеет равновесную нагрузочную способность, приближающуюся к 1 моль CO2 на моль амина.

ORGAL F 4050 также требует меньше энергии для регенерации.
Чтобы объединить преимущества ORGAL F 4050 и более мелких аминов, MDEA обычно смешивают с каталитическим промотором, таким как пиперазин, PZ, или быстрореагирующим амином, таким как MEA, чтобы сохранить реакционную способность, но снизить затраты на регенерацию.
ORGAL F 4050 или aMDEA использует пиперазин в качестве катализатора для увеличения скорости реакции с CO2.

ORGAL F 4050 был коммерчески успешным.
Было проведено множество тестов на эффективность ORGAL F 4050 или смесей MDEA/piperazine по сравнению с одиночными аминами.
Скорость производства CO2 была выше, чем у ORGAL F 4050 при той же тепловой мощности и общей молярной концентрации, когда эксперименты проводились на пилотной установке Университета Реджайны, которая была смоделирована по образцу завода по производству природного газа.

Также были обнаружены незначительные следовые количества продуктов распада.
Однако, когда те же контрольные переменные и испытания были проведены на электростанции Boundary Dam, скорость производства CO2 для смешанного растворителя была ниже, чем у ORGAL F 4050.
Это произошло в результате снижения способности растворителя поглощать CO2 после разложения.

Поскольку Boundary Dam является угольной электростанцией, она работает в более суровых условиях и производит нечистые дымовые газы, содержащие летучую золу, SO2 и NO2, которые подаются на улавливание углерода.
Даже при предварительной обработке дымовых газов их все еще достаточно для производства продуктов разложения, таких как амины с прямой цепью и соединения серы, которые накапливаются, поэтому регенерация ORGAL F 4050 и MDEA больше невозможна.
Чтобы эти смеси успешно снижали тепловую нагрузку, необходимо поддерживать их химическую стабильность.

Использует:
ORGAL F 4050 используется в защитных покрытиях для печатных плат для предотвращения попадания влаги и пыли, обеспечивая надежную работу.
Обеспечивает защитную герметизацию электронных компонентов, защищая их от воздействия факторов окружающей среды.
ORGAL F 4050 используется в покрытиях для кухонных шкафов и шкафов для ванных комнат для обеспечения прочной, влагостойкой отделки.

Обеспечивает устойчивость к ультрафиолетовому излучению и атмосферным воздействиям для уличной деревянной мебели, сохраняя внешний вид и структурную целостность.
ORGAL F 4050 используется в качестве связующего вещества в печатных красках для обеспечения хорошей адгезии, сохранения цвета и качества печати.
Наносится в качестве защитного слоя на печатные материалы для усиления блеска и стойкости к истиранию.

ORGAL F 4050 используется в покрытиях для EIFS для обеспечения защитного, атмосферостойкого покрытия.
Применяется на крышах для обеспечения гидроизоляции, защиты от ультрафиолета и увеличения срока службы.
ORGAL F 4050 используется в покрытиях для бытовой техники, такой как холодильники и стиральные машины, обеспечивая долговечность и очищаемую поверхность.

Обеспечивает безопасную, прочную и яркую отделку детских игрушек и оборудования для игровых площадок.
ORGAL F 4050 используется в покрытиях для сельскохозяйственной техники и оборудования, обеспечивая защиту от атмосферных воздействий, химических веществ и механического износа.
Применяется в покрытиях для тепличных конструкций для обеспечения защиты от ультрафиолета и долговечности.

ORGAL F 4050 используется в покрытиях для упаковочных материалов для пищевых продуктов для обеспечения влагостойкости и сохранения целостности продукта.
Обеспечивает защитные покрытия для промышленных упаковочных материалов, обеспечивая долговечность при транспортировке и хранении.
ORGAL F 4050 используется в покрытиях для медицинских приборов и оборудования для обеспечения долговечной, стерилизуемой отделки.

Применяется в покрытиях для гигиенических изделий, таких как одноразовые перчатки и халаты, обеспечивая барьерные свойства и долговечность.
Формулируется в художественных красках для использования в изобразительном искусстве, обеспечивая яркие цвета и отличную обрабатываемость.
ORGAL F 4050 используется в покрытиях для различных ремесленных материалов, обеспечивая долговечность и эстетическое улучшение.

Наносится на стены и полы подвала для обеспечения водонепроницаемого барьера и предотвращения проникновения влаги.
Обеспечивает гидроизоляцию и защиту от ультрафиолета открытых наружных поверхностей.

ORGAL F 4050 используется в составах, которые позволяют легко удалять граффити, защищая поверхности от вандализма.
Входит в состав покрытий, которые обеспечивают теплоизоляционные свойства для энергоэффективности в зданиях.

ORGAL F 4050 - это специальный полимер на основе акриловой эмульсии, предназначенный для использования в различных покрытиях и клеях.
ORGAL F 4050 обычно используется в составах, требующих баланса между эксплуатационными характеристиками и соблюдением экологических норм.
ORGAL F 4050 можно использовать в сочетании с другими полимерами и добавками для достижения желаемых свойств в конечном продукте.

ORGAL F 4050 используется в рецептурах красок для внутренних стен, которые требуют хорошей моющейся способности, устойчивости к пятнам и эстетической привлекательности.
Идеально подходит для наружных покрытий благодаря своей устойчивости к ультрафиолетовому излучению и долговечности, защищая поверхности от суровых погодных условий.
Обеспечивает отличную адгезию и коррозионную стойкость для металлических поверхностей, подходит для промышленного оборудования и конструкций.

Используется в покрытиях для бетонных полов и стен, обеспечивая долговечность и устойчивость к истиранию и химическим веществам.
ORGAL F 4050 используется в производстве лент, этикеток и наклеек благодаря своим сильным адгезионным свойствам к липкости и отслаиванию.
Разработан для прочного сцепления с такими строительными материалами, как дерево, металл и пластик.

Применяется в упаковке для склеивания различных материалов, таких как бумага, картон и пластик.
Наносится на ткани для обеспечения водонепроницаемости, огнестойкости и повышенной прочности без ущерба для текстуры и гибкости.
ORGAL F 4050 используется в качестве связующего вещества в нетканых материалах для гигиенических изделий, фильтрующих материалов и геотекстиля, обеспечивая прочность и структурную целостность.

Входит в состав герметиков для герметизации швов и щелей в зданиях, обеспечивая гибкость, устойчивость к атмосферным воздействиям и адгезию к различным основаниям.
ORGAL F 4050 используется в автомобильной промышленности для герметизации швов и соединений, обеспечивая долговечность и устойчивость к воздействию тепла и автомобильных жидкостей.
ORGAL F 4050 используется в защитных покрытиях для различных поверхностей, обеспечивая устойчивость к факторам окружающей среды, таким как влага, химические вещества и истирание.

Разработан для декоративных целей, обеспечивая эстетическую отделку с долговечностью и защитой.
Применяется в покрытиях из бумаги и картона для улучшения таких свойств, как блеск, гладкость и пригодность для печати.
ORGAL F 4050 используется в упаковочных пленках для придания барьерных свойств и улучшения внешнего вида упакованных товаров.

ORGAL F 4050 используется в качестве модификатора в цементных и бетонных составах для улучшения таких свойств, как адгезия, гибкость и долговечность.
В состав входят клеи для плитки, обеспечивающие прочное сцепление и устойчивость к влаге и перепадам температуры.
ORGAL F 4050 используется в покрытиях для деревянной мебели для улучшения внешнего вида, защиты от износа, а также обеспечения устойчивости к факторам окружающей среды.

Применяется в покрытиях для деревянных полов для долговечности, устойчивости к царапинам и простоте ухода.
ORGAL F 4050 используется в автомобильных красках и покрытиях благодаря своей превосходной адгезии, долговечности и устойчивости к факторам окружающей среды.
Входит в состав покрытий для внутренних автомобильных компонентов для обеспечения долговечной и эстетически привлекательной отделки.

ORGAL F 4050 используется в покрытиях для лодок и морских сооружений, обеспечивая защиту от воды, соли и других суровых морских условий.
Применяется в покрытиях для промышленного оборудования для защиты от износа, коррозии и химического воздействия.
ORGAL F 4050 используется в покрытиях для различного промышленного оборудования, обеспечивая долговечность и устойчивость к суровым условиям эксплуатации.

Разработан в продуктах «сделай сам» для ремонта и благоустройства дома, обеспечивает простоту нанесения и надежную работу.
ORGAL F 4050 используется в декоративной отделке для домашних интерьеров и экстерьеров, обеспечивая как защиту, так и эстетическое улучшение.
Идеально подходит для использования в красках для потолков благодаря своей способности обеспечивать гладкое, матовое покрытие с отличным покрытием.

ORGAL F 4050 используется в качестве базового покрытия для подготовки поверхностей к покраске, обеспечивая лучшую адгезию и равномерное покрытие.
Обеспечивает длительную защиту машин и оборудования, работающих в суровых промышленных условиях.
Обеспечивает защитный барьер для предотвращения ржавчины и коррозии на металлических поверхностях.

ORGAL F 4050 используется в покрытиях днища автомобилей для защиты от коррозии, дорожных солей и механических повреждений.
Обеспечивает хорошую адгезию и долговечность на пластиковых деталях, используемых в автомобильных интерьерах и экстерьерах.
Применяется на корпусах лодок и кораблей для защиты от повреждений водой, обрастания и морской растительности.

Обеспечивает нескользящую, прочную поверхность на палубах судов, способную выдерживать суровые морские условия.
ORGAL F 4050 используется в покрытиях для интерьеров самолетов, обеспечивая прочную и эстетически приятную отделку, отвечающую строгим авиационным стандартам.
Обеспечивает защиту наружных поверхностей самолета от факторов окружающей среды и механического износа.

Профиль безопасности:
ORGAL F 4050 используется в хорошо проветриваемых помещениях или с соответствующими средствами защиты органов дыхания.
ORGAL F 4050 - это защитные очки или лицевой щиток для защиты глаз.
Вдыхание аэрозоля или тумана может вызвать раздражение дыхательных путей.

Не ешьте, не пейте и не курите при использовании этого продукта.
Тщательно вымойте руки после работы.
Несмотря на то, что в целом в нем мало летучих органических соединений, неправильная утилизация может оказать воздействие на окружающую среду.

Избегайте попадания в окружающую среду.
Утилизируйте содержимое/контейнер в соответствии с местными правилами.
Вымойте большим количеством воды с мылом.

При появлении раздражения кожи или сыпи обратитесь за медицинской помощью.
Осторожно смойте водой в течение нескольких минут.
Снимите контактные линзы, если они есть и это легко сделать.

Если раздражение глаз не проходит, обратитесь за медицинской помощью.
Выведите человека на свежий воздух и держите его удобным для дыхания.
Если дыхание затруднено, немедленно обратитесь за медицинской помощью.

Длительный или повторный контакт с кожей может вызвать раздражение или дерматит.
Надевайте защитные перчатки и избегайте прямого контакта с кожей.
Может вызвать раздражение глаз при контакте.


ORGAL HYDROFLEX 57
Orgal Hydroflex 57 представляет собой не содержащую пластификаторов и не содержащую APEO анионно-неионную водную дисперсию на основе стирола и эфира акриловой кислоты.
Orgal Hydroflex 57 широко распространен на всех рынках, где используются системы на водной основе, благодаря множеству специфических свойств, которых можно достичь.


Химическое название: Стирол-акриловый сополимер.


Orgal Hydroflex 57 основан на группе химикатов, которые являются настоящими «рабочими лошадками» в области химии полимеров.
Orgal Hydroflex 57 известен как акрилаты, в эту группу входят акриловая кислота и ее эфиры — метилакрилат, бутилакрилат, этилакрилат и 2-этилгексилакрилат.


Все эти акриловые мономеры являются высокореактивными химическими веществами, что означает, что они легко соединяются сами с собой или с другими мономерами с образованием коммерчески важных полимеров.
Одна из наиболее важных полимерных реакций, происходящая посредством эмульсионной полимеризации, включает соединение мономеров на акриловой основе со стиролом с образованием Orgal Hydroflex 57.


Универсальность этого класса полимеров во многом обязана широкому семейству акриловых мономеров, которые в сочетании со стиролом могут образовывать статистические сополимеры с определенными температурами стеклования (Tg).
Orgal Hydroflex 57 широко распространен на всех рынках, где используются системы на водной основе, благодаря множеству специфических свойств, которых можно достичь.


Orgal Hydroflex 57 представляет собой дисперсионную эмульсию стирола-акрилового сополимера на водной основе.
Orgal Hydroflex 57 представляет собой стабилизированную поверхностно-активными веществами не содержащую коллоидов эмульсию, которая обладает превосходными характеристиками загрузки пигментов, устойчивостью к щелочам и хорошей связующей способностью для удержания текстурных агрегатов.


Orgal Hydroflex 57 представляет собой группу полимеров, обычно получаемых путем полимеризации комбинации стирола и акриловых мономеров.
Эти полимеры обладают смесью свойств, полученных как от акриловых, так и от стирольных компонентов.
Это составы на водной основе, которые диспергируются в воде с образованием стабильных эмульсий.


Благодаря отличным адгезионным, прочным и пленкообразующим свойствам Orgal Hydroflex 57 имеет широкий спектр применения в различных отраслях промышленности.
Orgal Hydroflex 57 представляет собой эмульсию стирольно-акрилового сополимера с низким содержанием APEO, аммиака и формальдегида, которая образует прозрачную, эластичную и слегка липкую пленку при высыхании при температуре выше 0°C.


Orgal Hydroflex 57 хорошо совместим с цементными смесями.
Orgal Hydroflex 57 обеспечивает лучшую реологию раствора, уменьшает образование трещин в растворах, а после отверждения улучшает адгезию, гибкость, водостойкость и способность перекрывать трещины.


Orgal Hydroflex 57 представляет собой стирол-акриловый сополимер, не содержащий APEO, аммиака и формальдегида, с низкой Tg, который образует прозрачную, эластичную и слегка липкую пленку при высыхании при температуре выше 0°C.
Orgal Hydroflex 57 хорошо совместим с цементными смесями.


Orgal Hydroflex 57 обеспечивает лучшую реологию раствора, снижает
образование трещин в строительных растворах и после затвердевания улучшает адгезию, гибкость, водостойкость и способность перекрывать трещины.
Orgal Hydroflex 57 представляет собой стирол-акриловую сополимерную эмульсию, не содержащую APEO, аммиака и формальдегида, с низким Tg.


Orgal Hydroflex 57 образует прозрачную, эластичную и липкую пленку при высыхании при температуре выше 0°C.
Orgal Hydroflex 57 хорошо совместим с цементными смесями.
Orgal Hydroflex 57 обеспечивает лучшую реологию раствора, уменьшает растрескивание, улучшает адгезию, гибкость, водостойкость и устойчивость к растрескиванию.



ИСПОЛЬЗОВАНИЕ И ПРИМЕНЕНИЕ ORGAL HYDROFLEX 57:
Настоятельно рекомендуется для производства матовых, полуглянцевых красок и грунтовок благодаря превосходной стойкости к истиранию и высокой способности связывания пигментов Orgal Hydroflex 57.
Рекомендуется для шпаклевок, герметиков и акриловой штукатурки из-за превосходной водостойкости Orgal Hydroflex 57.
Orgal Hydroflex 57 можно использовать с клеями для керамической плитки на основе дисперсии и клеями ETIC благодаря их превосходной адгезионной способности.


Orgal Hydroflex 57 используется в качестве связующего вещества в красках на водной основе для архитектурных красок (внутреннее и наружное применение).
Orgal Hydroflex 57 в основном используется во внутренних латексных красках, внутренних клеях для керамической плитки, шпатлевках, шпаклевках и эластомерных кровельных покрытиях, изготовленных из стирольно-акрилового сополимера.


Также используются вторичные связующие из стекловолокна, например, для настенных покрытий.
Orgal Hydroflex 57 обеспечивает превосходный блеск, прочность пленки, долговечность и стойкость к удалению моющими средствами.
Orgal Hydroflex 57 обеспечивает высокую устойчивость к ультрафиолетовому излучению и устойчивость к воде и щелочам.


Orgal Hydroflex 57 считается важным компонентом напольной отделки.
Orgal Hydroflex 57 в основном используется в архитектурных/декоративных красках для внутренних и наружных стен, глянцевых красках для кухни и ванны, фасадов и т. д.


Orgal Hydroflex 57 используется в деревообрабатывающей и мебельной промышленности.
Благодаря превосходным связующим свойствам пигментов в красках для внутренних и наружных работ в качестве связующего используется Orgal Hydroflex 57.
Orgal Hydroflex 57 обеспечивает идеальный блеск, прочность пленки, долговечность и химическую стойкость.


Покрытия Orgal Hydroflex 57 обеспечивают высокую устойчивость к ультрафиолетовому излучению, а также устойчивость к воде и щелочам.
Orgal Hydroflex 57 невероятно долговечен.
Важно знать, что добавление стирола в Orgal Hydroflex 57 может снизить водопоглощение и гибкость пленки.


Этот тип покрытия требует относительно небольшого ухода благодаря низкой склонности Orgal Hydroflex 57 к собиранию грязи, а также исключительной гибкости и долговечности пленки.
Используется Orgal Hydroflex 57, обеспечивающий сильную адгезию, отличные характеристики загрузки пигмента и устойчивость к щелочам.


Несмотря на эти недостатки, Orgal Hydroflex 57 по-прежнему широко используется в строительных продуктах, таких как клеи для керамической плитки, шпатлевки, шпаклевки и эластомерные кровельные покрытия.
Orgal Hydroflex 57 также используется во вторичных связующих для стекловолокна, таких как настенные покрытия и архитектурные декоративные покрытия.


Orgal Hydroflex 57 улучшает реологию раствора, адгезию, гибкость, водостойкость и способность перекрывать трещины.
Orgal Hydroflex 57 безопасен для систем, контактирующих с питьевой водой.
Orgal Hydroflex 57 используется в 2К цементных гидроизоляционных растворах.


Orgal Hydroflex 57 применяется для цементных плиточных клеев 2K (тип S2).
Orgal Hydroflex 57 используется в гидроизоляционных системах на основе 1К или 2К битума.
Orgal Hydroflex 57 — это стирол-акриловая эмульсия, не содержащая APEO, аммиака и формальдегида.


Orgal Hydroflex 57 имеет низкий Tg и образует прозрачную, эластичную и слегка липкую пленку.
Orgal Hydroflex 57 – новый экологически чистый полимер для эластичных строительных растворов.
Orgal Hydroflex 57 также обеспечивает лучшую реологию раствора, уменьшает образование трещин и улучшает адгезию и гибкость.


Orgal Hydroflex 57 представляет собой линейку полимерных эмульсий на основе акриловой, стирол-акриловой и винилакриловой химии.
Orgal Hydroflex 57 соответствует нормам ЛОС, поэтапно отказываясь от формальдегида, аммиака и других ограниченных веществ.
Orgal Hydroflex 57 используется для производства цементных гидроизоляционных растворов, цементных клеев для плитки и гидроизоляционных систем на битумной основе.


Orgal Hydroflex 57 можно использовать в системах, контактирующих с питьевой водой.
Orgal Hydroflex 57 используется в качестве связующего для красок для внутренних и наружных работ благодаря своим выдающимся свойствам связывания пигментов.
Orgal Hydroflex 57 обеспечивает идеальный блеск, прочность пленки, долговечность и стойкость к удалению моющими с��едствами.


Покрытия на основе Orgal Hydroflex 57 обладают превосходной устойчивостью к ультрафиолетовому излучению, а также устойчивостью к воде и щелочам.
Важно отметить, что увеличение содержания стирола в Orgal Hydroflex 57 может ухудшить водопоглощение и эластичность пленки.
Эти покрытия требуют минимального ухода, поскольку имеют низкую склонность к загрязнению и обладают хорошей гибкостью и твердостью пленки.


Orgal Hydroflex 57 считается важным компонентом напольной отделки.
Orgal Hydroflex 57 в основном используется в архитектурных/декоративных красках для внутренних и наружных стеновых покрытий, глянцевых красках для кухонь и ванных комнат, фасадов и т. д., а также в деревообрабатывающей и мебельной промышленности.


-Использование красок и покрытий Orgal Hydroflex 57:
Orgal Hydroflex 57 в основном используется в качестве связующего вещества в красках и покрытиях на водной основе.
Orgal Hydroflex 57 предлагает множество преимуществ и играет важную роль в обеспечении необходимых свойств красок и покрытий.

Orgal Hydroflex 57 обеспечивает отличную адгезию, позволяя краске прочно сцепляться с различными поверхностями, такими как металл, дерево, пластик и бетон.
Orgal Hydroflex 57 также способствует образованию пленки при высыхании краски или покрытия на водной основе.

Эта пленка образует защитный слой, который обеспечивает долговечность, прочность и устойчивость покрытия к атмосферным воздействиям.
Пленка также может помочь предотвратить воздействие химикатов, влаги и загрязнений на нижележащее основание.


-Использование Orgal Hydroflex 57 в строительстве:
Orgal Hydroflex 57 обычно используется в рецептурах строительных материалов для улучшения прочности сцепления между подложками и обеспечения гибкости.
При добавлении в строительные растворы и затирки Orgal Hydroflex 57 может помочь улучшить адгезию, долговечность и гибкость.

Orgal Hydroflex 57 улучшает прочность сцепления между раствором или затиркой и основанием, что делает их идеальными для таких применений, как ремонт каменной кладки, приклеивание плитки и других строительных проектов.
Orgal Hydroflex 57 также можно использовать в качестве добавки в составы бетона и цемента для повышения удобоукладываемости, прочности и долговечности.


- Эмульсионные полимеры используют Orgal Hydroflex 57:
Orgal Hydroflex 57 можно использовать в качестве эмульсионных полимеров благодаря их способности диспергироваться в воде и создавать стабильные эмульсии.
Orgal Hydroflex 57 может использоваться в качестве ингредиента при производстве синтетического каучука.

Orgal Hydroflex 57 используется в качестве связующего эмульсии для улучшения свойств резиновых смесей, таких как гибкость, адгезия, стойкость к химическим веществам и истиранию.

При добавлении в текстильные покрытия Orgal Hydroflex 57 обеспечивает широкий спектр функциональных возможностей.
Orgal Hydroflex 57 повышает устойчивость к воде, адгезии и пятнам, а также повышает прочность и долговечность материала.



ДРУГИЕ СВОЙСТВА ORGAL HYDROFLEX 57:
* Хорошая устойчивость к атмосферным воздействиям и хорошая устойчивость к пятнам.
* Широкий баланс растяжения/удлинения
*Возможность перекрестных ссылок
*Высокая пигментсвязывающая способность
*Идеальный блеск, прочность пленки и стойкость к удалению моющими средствами.
*Хорошая адгезия к обычным основаниям, включая оцинкованную сталь, алюминий и дерево.
*Одним из недостатков Orgal Hydroflex 57 является склонность к пожелтению под воздействием прямых солнечных лучей.
Фактически, с увеличением содержания стирола пожелтение усиливается, хотя влияние могут иметь и другие факторы.
Например, свободнорадикальные инициаторы полимеризации Orgal Hydroflex 57 могут влиять на степень пожелтения конечного продукта.



ЖЕЛАЕМЫЕ СВОЙСТВА ОРГАЛА ГИДРОФЛЕКС 57:
Orgal Hydroflex 57 обладает превосходными гидрофобными характеристиками, что означает, что они обладают превосходной водостойкостью и скоростью пропускания паров влаги (MVTR) по сравнению с полностью акриловыми полимерами.
Кроме того, сам стирол является гидрофобным мономером, что позволяет производить Orgal Hydroflex 57 с низким размером частиц.

В результате появляются полимеры, которые идеально подходят для определенных применений, например, в качестве грунтовок для строительной промышленности или связующих веществ для покрытий бумаги.
Еще одним важным свойством Orgal Hydroflex 57 является высокая температура стеклования.
В результате Orgal Hydroflex 57 отличается долговечностью, хорошей стойкостью к истиранию и хорошими механическими свойствами.



ОСНОВНЫЕ ХАРАКТЕРИСТИКИ И ПРИМЕНЕНИЯ ORGAL HYDROFLEX 57:
*Грунты, штукатурки, текстурированные и настенные краски для архитектурных покрытий.
*Внутренние и наружные покрытия из дерева и металла.
* Высокая производительность и долговечность для домашнего и промышленного использования.
*Системы влажной адгезии, самосшивки и блокировки пятен.
*Марки общего назначения действуют как загустители, имеющие псевдопластичный профиль.



ПРЕИМУЩЕСТВА ORGAL HYDROFLEX 57:
*Высокая пигментсвязывающая способность и устойчивость к щелочам.
*Положительное влияние на интенсивность цвета и устойчивость к истиранию.
* Не содержит APEO и формальдегида для здорового применения внутри помещений.
* Простота в обращении, широкое применение.
*Технология производства автоматизации и стабильное качество



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ОРГАЛА ГИДРОФЛЕКС 57:
Внешний вид: Белая эмульсия
Твердое содержание (%_1) +: 57
Вязкость RVT 3/60: макс. 700 сП.
pH: 7,0–9,0
Плотность (25°С, г/см3) ±0,01:1,04
MFFT (°C): < 0
Тс (°С): -10
Стабильность при хранении: Беречь от замерзания.



МЕРЫ ПЕРВОЙ ПОМОЩИ ОРГАЛА ГИДРОФЛЕКС 57:
-Описание мер первой помощи.
*Общие советы:
Покажите этот паспорт безопасности материала лечащему врачу.
*При вдыхании:
После ингаляции:
Свежий воздух.
*При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промыть кожу с
вода/душ.
*В случае зрительного контакта:
После зрительного контакта:
Промойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.
*При проглатывании:
После глотания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.
-Указание на необходимость немедленной медицинской помощи и специального лечения.
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ ORGAL HYDROFLEX 57:
-Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Закройте дренажи.
Соберите, свяжите и откачайте пролитую жидкость.
Соблюдайте возможные ограничения по материалам.
Возьмите в сухом виде.
Утилизируйте должным образом.
Очистите пораженное место.



МЕРЫ ПОЖАРОТУШЕНИЯ ORGAL HYDROFLEX 57:
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Углекислый газ (CO2)
Мыло
Сухой порошок
*Неподходящие средства пожаротушения:
Для этого вещества/смеси не установлены ограничения по огнетушащим веществам.
-Дальнейшая информация:
Не допускайте попадания воды для пожаротушения в поверхностные воды или систему грунтовых вод.



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/ПЕРСОНАЛЬНАЯ ЗАЩИТА ORGAL HYDROFLEX 57:
-Параметры управления:
--Ингредиенты с параметрами контроля на рабочем месте:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
*Защита глаз/лица:
Используйте средства защиты глаз.
Безопасные очки
*Защита тела:
защитная одежда
*Защита органов дыхания:
Рекомендуемый тип фильтра: Фильтр A
-Контроль воздействия на окружающую среду:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ORGAL HYDROFLEX 57:
-Условия безопасного хранения, включая любые несовместимости:
*Условия хранения:
Плотно закрыто.
Сухой.



СТАБИЛЬНОСТЬ И РЕАКЦИОННАЯ СПОСОБНОСТЬ ORGAL HYDROFLEX 57:
-Химическая стабильность:
Продукт химически стабилен при стандартных условиях окружающей среды (комнатная температура).
-Возможность опасных реакций:
Данные недоступны


ORGAL K 411
Orgal K 411 представляет собой акриловую эмульсию, не содержащую APEO и пластификаторов, обладающую свойствами мягкой и пластичной пленки.


Тип продукта: Акрилы и акриловые сополимеры > Акриловые эмульсии
Химический состав: Акриловая эмульсия.


Акриловая композиция обеспечивает очень хорошую гибкость и долговременную стойкость к атмосферным воздействиям, что приводит к сохранению белизны, адгезии и гибкости при старении.


Orgal K 411 используется в рецептурах кровельных покрытий и везде, где требуется гибкий полимер с высоким содержанием сухого остатка, очень хорошей адгезией и долговечностью.
Orgal K 411 представляет собой акриловую эмульсию, не содержащую APEO и пластификаторов, обладающую свойствами мягкой и пластичной пленки.



ИСПОЛЬЗОВАНИЕ И ПРИМЕНЕНИЕ ORGAL K 411:
Области применения Orgal K 411: герметики, герметики и клеи для полов и ковров.
Orgal K 411 используется в рецептурах кровельных покрытий и везде, где требуется гибкий полимер с высоким содержанием сухого остатка, очень хорошей адгезией и долговечностью.



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ОРГАЛА К 411:
Название продукта: ОРГАЛ К 411
Химический состав: Акриловая эмульсия.
Всего твердых веществ (% ±1%): 59
рН: 6,0
Вязкость (мПа.с макс.): 1000
MFFT (°C): <0
Тс (°С): -36
Тип продукта: Акрилы и акриловые сополимеры > Акриловые эмульсии
Физическая форма: Эмульсия



МЕРЫ ПЕРВОЙ ПОМОЩИ ОРГАЛА К 411:
-Описание мер первой помощи.
*Общие советы:
Покажите этот паспорт безопасности материала лечащему врачу.
*При вдыхании:
После ингаляции:
Свежий воздух.
*При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промыть кожу с
вода/душ.
*В случае зрительного контакта:
После зрительного контакта:
Промойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.
*При проглатывании:
После глотания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.
-Указание на необходимость немедленной медицинской помощи и специального лечения.
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ ORGAL K 411:
-Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Закройте дренажи.
Соберите, свяжите и откачайте пролитую жидкость.
Соблюдайте возможные ограничения по материалам.
Возьмите в сухом виде.
Утилизируйте должным образом.
Очистите пораженное место.



МЕРЫ ПОЖАРОТУШЕНИЯ ORGAL K 411:
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Углекислый газ (CO2)
Мыло
Сухой порошок
*Неподходящие средства пожаротушения:
Для этого вещества/смеси не установлены ограничения по огнетушащим веществам.
-Дальнейшая информация:
Не допускайте попадания воды для пожаротушения в поверхностные воды или систему грунтовых вод.



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/ПЕРСОНАЛЬНАЯ ЗАЩИТА ORGAL K 411:
-Параметры управления:
--Ингредиенты с параметрами контроля на рабочем месте:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
*Защита глаз/лица:
Используйте средства защиты глаз.
Безопасные очки
*Защита тела:
защитная одежда
*Защита органов дыхания:
Рекомендуемый тип фильтра: Фильтр A
-Контроль воздействия на окружающую среду:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ОРГАЛА К 411:
-Условия безопасного хранения, включая любые несовместимости:
*Условия хранения:
Плотно закрыто.
Сухой.



СТАБИЛЬНОСТЬ И РЕАКЦИОННАЯ СПОСОБНОСТЬ ОРГАЛА К 411:
-Химическая стабильность:
Продукт химически стабилен при стандартных условиях окружающей среды (комнатная температура).
-Возможность опасных реакций:
Данные недоступны


ORGAL P 062V
Orgal P 062V — это акриловые, винилакриловые и стиролакриловые полимерные эмульсии, не содержащие APEO и MIT, для внутренних и наружных настенных покрытий и художественных красок.


Тип продукта: Акрилы и акриловые сополимеры > Винил-акрил
Химический состав: Винил-акриловая сополимерная эмульсия


Orgal P 062V — это дисперсия винил-акрилового сополимера с низкой излучательной способностью, не содержащая APEO, специально разработанная для использования в производстве экологически чистых красок для внутренних работ, не содержащих растворителей, обладающих превосходной гидрофобностью и стойкостью к мокрому истиранию, отличной укрывистостью, хорошей адгезией и слабый запах.
Orgal P 062V — это акриловые, винилакриловые и стиролакриловые полимерные эмульсии, не содержащие APEO и MIT, для внутренних и наружных настенных покрытий и художественных красок.


Orgal P 062V представляет собой сополимер винилацетата и акрила.
Orgal P 062V имеет эмульсию винил-акрилового сополимера с низким уровнем эмиссии, не содержащую APEO.



ИСПОЛЬЗОВАНИЕ И ПРИМЕНЕНИЕ ORGAL P 062V:
Orgal P 062V можно использовать в качестве связующего для всех типов низкоэмиссионных настенных покрытий.
Краски, не содержащие летучих органических соединений на основе и с Orgal P 062V, обладают превосходной стойкостью к истиранию, трещиностойкости, стойкости к образованию пятен во всех составах красок, не содержащих растворителей, в диапазоне среднего и высокого содержания OCP.


Orgal P 062V — это дисперсия винил-акрилового сополимера с низкой излучательной способностью, не содержащая APEO, специально разработанная для использования в производстве экологически чистых красок для внутренних работ, не содержащих растворителей, обладающих превосходной гидрофобностью и стойкостью к мокрому истиранию, отличной укрывистостью, хорошей адгезией и слабый запах.
Orgal P 062V используется в составах красок с низким содержанием летучих органических соединений (ЛОС), в красках, не содержащих растворителей, где хорошее пленкообразование достигается без использования коалесцентов.


Применение и использование Orgal P 062V: рынки, строительство.
Области применения Orgal P 062V: химическая стойкость,
Краски для самостоятельного изготовления, глянцевые краски/краски для отделки, столярные покрытия, шлифуемые герметики/грунтовки и морилки для дерева


Orgal P 062V используется в строительстве: ограждающие конструкции и кровельные покрытия, а также архитектурные покрытия.
Orgal P 062V — это дисперсия винил-акрилового сополимера с низкой излучательной способностью, не содержащая APEO, специально разработанная для использования в производстве экологически чистых красок для внутренних работ, не содержащих растворителей, с превосходной гидрофобностью и стойкостью к мокрому истиранию, отличной укрывистостью, хорошей адгезией и низкой запах.


Orgal P 062V используется в составах красок с низким содержанием летучих органических соединений (ЛОС), в красках, не содержащих растворителей, где хорошее пленкообразование достигается без использования коалесцентов.
Области применения Orgal P 062V: матовые краски, не содержащие растворителей.


Orgal P 062V используется в качестве основного связующего для всех видов красок для стен с низким уровнем выбросов.
Orgal P 062V специально разработан для использования в красках для стен, не содержащих растворителей, с очень хорошей водостойкостью и стойкостью к истиранию, очень хорошими эксплуатационными свойствами, хорошей адгезией и слабым запахом.


При составлении красок с низким содержанием летучих органических соединений и без растворителей хорошее образование пленки может быть достигнуто без коалесцирующих добавок.
Краски, не содержащие летучих органических соединений, изготовленные на основе Orgal P 062V, обеспечивают очень хорошую стойкость к истиранию, устойчивость к образованию грязевых трещин в составах, не содержащих растворителей, от среднего до высокого диапазона ПВХ.
Orgal P 062V отличается образованием пленки без коалесцентов, низким впитыванием грязи, очень хорошей адгезией и водостойкостью.



ХАРАКТЕРИСТИКИ ORGAL P 062V:
*Интерьерные краски
*Отличный



ХИМИЧЕСКАЯ СЕМЬЯ ORGAL P 062V:
*Акрилы,
*Акрилаты и метакрилаты,
*Винилы,
* Винилы и производные винила



ТИП ПРОДУКТА ORGAL P 062V:
*Покрытие
*Технологии
*Готовые к использованию продукты



СЕМЕЙСТВО ПРОДУКТОВ ORGAL P 062V:
*Готовая к использованию продукция — краски и покрытия.
*Другие краски и покрытия



ОСОБЕННОСТИ И ПРЕИМУЩЕСТВА ORGAL P 062V:
*Маркировка претензий
*Без формальдегида,
* Низкий уровень летучих органических соединений,
*Другие заявления о маркировке



ХАРАКТЕРИСТИКИ ОРГАЛА П 062В:
*Отличная стойкость к истиранию
*Пленкообразование без коалесцентов.
*Отличная адгезия
*Отличная водостойкость
*Не содержит APEO, формальдегида и аммиака.
*Отличная устойчивость к загрязнениям и трещинам.
* Низкое накопление пыли
* Легко наносится.



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ОРГАЛА П 062В:
Химический состав: переменный ток
Всего твердых веществ (% ±1): 43
рН: 7,5
Вязкость (мПа.с макс): 400
MFFT (°C): 14
Тс (°С): 25
Внешний вид: Белая вязкая жидкость.
Продукт 2: ОРГАЛ П 062В
Химический состав: ВА/АС
Всего твердых веществ (% ±1): 53
рН: 4,0
Вязкость (мПа.с макс): 4000

MFFT (°C): <3
Тс (°С): 11
Внешний вид: Белая эмульсия
Дополнительная информация (общая)
Внешний вид: Белая эмульсия
Всего твердых веществ (% ±1): 53
pH: 4,0–5,5
Вязкость (Brookfield RVT 3/20, мПа.с): 2500±1500
MFFT (°C): <3
Тс (°С): 11
Вязкость по Брукфилду (мПас): 2500 ± 1500
Производительность: Отлично подходит для внутренних красок.



МЕРЫ ПЕРВОЙ ПОМОЩИ ОРГАЛА П 062В:
-Описание мер первой помощи.
*Общие советы:
Покажите этот паспорт безопасности материала лечащему врачу.
*При вдыхании:
После ингаляции:
Свежий воздух.
*При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промыть кожу с
вода/душ.
*В случае зрительного контакта:
После зрительного контакта:
Промойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.
*При проглатывании:
После глотания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.
-Указание на необходимость немедленной медицинской помощи и специального лечения.
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ ORGAL P 062V:
-Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Закройте дренажи.
Соберите, свяжите и откачайте пролитую жидкость.
Соблюдайте возможные ограничения по материалам.
Возьмите в сухом виде.
Утилизируйте должным образом.
Очистите пораженное место.



МЕРЫ ПОЖАРОТУШЕНИЯ ОРГАЛА П 062В:
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Углекислый газ (CO2)
Мыло
Сухой порошок
*Неподходящие средства пожаротушения:
Для этого вещества/смеси не установлены ограничения по огнетушащим веществам.
-Дальнейшая информация:
Не допускайте попадания воды для пожаротушения в поверхностные воды или систему грунтовых вод.



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/ПЕРСОНАЛЬНАЯ ЗАЩИТА ORGAL P 062V:
-Параметры управления:
--Ингредиенты с параметрами контроля на рабочем месте:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
*Защита глаз/лица:
Используйте средства защиты глаз.
Безопасные очки
*Защита тела:
защитная одежда
*Защита органов дыхания:
Рекомендуемый тип фильтра: Фильтр A
-Контроль воздействия на окружающую среду:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ORGAL P 062V:
-Условия безопасного хранения, включая любые несовместимости:
*Условия хранения:
Плотно закрыто.
Сухой.



СТАБИЛЬНОСТЬ И РЕАКЦИОННАЯ СПОСОБНОСТЬ ОРГАЛА П 062В:
-Химическая стабильность:
Продукт химически стабилен при стандартных условиях окружающей среды (комнатная температура).
-Возможность опасных реакций:
Данные недоступны

ORGAL P 526
Orgal P 526 обладает хорошей способностью связывать пигменты.
Orgal P 526 представляет собой сополимерную эмульсию винила и VeoVa.


Тип продукта: Винилы > Полимерные эмульсии винилацетата
Химический состав: Виниловая сополимерная эмульсия VeoVa.


Orgal P 526 представляет собой 55% сухого вещества, APEO, аммиак, пластификатор и свободную от коалесцирующих сополимеров эмульсию винилацетата и винилового эфира версатиновой кислоты (VeoVa).
Orgal P 526 действует как связующее для водных красок.


Orgal P 526 образует пленки без трещин при высыхании при температуре выше 11°C, прозрачные и обладающие хорошей гибкостью.
Orgal P 526 обладает очень хорошими глянцевыми свойствами, реологией, водостойкостью и связыванием пигментов.
Orgal P 526 представляет собой полностью высушенную пленку, обладающую хорошей устойчивостью к воде, щелочам и ультрафиолетовому излучению.


Orgal P 526 представляет собой сополимер винилацетата и винилверсатата.
Оргал П 526 представляет собой водную дисперсию сополимера на основе винилацетата и винилверсатата.
Orgal P 526 представляет собой сополимерную эмульсию винила и VeoVa.


Orgal P 526 образует прозрачные, эластичные пленки без трещин при высыхании при температуре выше 11°C.
Orgal P 526 не содержит APEO, аммиака, пластификаторов и коалесцентов.
Высушенная пленка обладает хорошей устойчивостью к воде, щелочам и ультрафиолетовому излучению.


Orgal P 526 обладает хорошей способностью связывать пигменты.
Orgal P 526 представляет собой свободную от APEO, аммиака, пластификатора и коалесцентную сополимерную эмульсию винилацетата и винилового эфира длинноцепочечной разветвленной карбоновой кислоты (VeoVa).


Orgal P 526 образует пленки без трещин при высыхании при температуре выше 11°C.
Пленки четкие, с хорошей гибкостью.
Оргал П 526 представляет собой мелкодисперсную эмульсию средней вязкости. Полностью высушенная пленка обладает хорошей устойчивостью к воде, щелочам и ультрафиолетовому излучению.


Orgal P 526 обладает хорошей способностью связывать пигменты и подходит для
производство наружных, внутренних красок, матовых, полуглянцевых, тиксотропных красок, штукатурок и текстурированных покрытий.
Оргал П 526 – водная дисперсия сополимера на основе винилацетата и винилверсатата.



ИСПОЛЬЗОВАНИЕ И ПРИМЕНЕНИЕ ORGAL P 526:
Orgal P 526 представляет собой терполимер винилацетата/винилового эфира длинноцепочечной разветвленной карбоновой кислоты и акрила, не содержащий APEO, аммиака, пластификаторов и коалесцентов.
Orgal P 526 обладает хорошей способностью связывания пигментов и подходит для изготовления наружных, внутренних красок, матовых, полуглянцевых, тиксотропных красок, штукатурок и текстурированных покрытий.


Водная дисперсия Оргал П 526 отличается высокой вяжущей способностью, хорошей водостойкостью и устойчивостью к омылению, рекомендуется для производства матовых и полуматовых красок для внутренних и наружных работ с хорошими реологическими свойствами.
Благодаря своим отличительным свойствам Orgal P 526 широко используется для производства огнезащитных ПК.


Применение Orgal P 526: Строительство: ограждающие конструкции и кровля, а также архитектурные покрытия.
Orgal P 526 образует пленки без трещин при высыхании при температуре выше 11°C.
Пленки четкие, с хорошей гибкостью.


Orgal P 526 обладает очень хорошими глянцевыми свойствами, реологией, водостойкостью и связыванием пигментов.
Orgal P 526 представляет собой полностью высушенную пленку, обладающую хорошей устойчивостью к воде, щелочам и ультрафиолетовому излучению.
Orgal P 526 используется для производства красок для внутренних и наружных работ, матовых, полуглянцевых, тиксотропных красок, штукатурок и текстурированных покрытий.



ХАРАКТЕРИСТИКИ ОРГАЛА П 526:
Оргал П 526 представляет собой дисперсию с мелким размером частиц и средней вязкостью.
Полностью высушенная пленка обладает хорошей водостойкостью, устойчивостью к щелочам и ультрафиолетовому излучению.

При высыхании выше 11°С на пленке не образуются трещины.
Полученная пленка имеет высокую белизну и хорошую гибкость.

Дисперсия имеет:
*Отличная реология;
*Хорошая водостойкость;
*Высокая когезионность пигмента;
*Широкий спектр применения.



СВОЙСТВА ОРГАЛА П 526:
 Очень хороший блеск
 Отличная реология
 Отличная водостойкость
 Отличное связывание пигментов
 Широкий спектр применения



ОБРАЩЕНИЕ – ХРАНЕНИЕ – СРОК ХРАНЕНИЯ ORGAL P 526:
Для обеспечения безопасного хранения Оргала П 526 контейнеры должны быть хорошо запечатаны во избежание испарения воды и образования пленки.
Оргал П 526 следует хранить при температуре 5–25°C не более 12 дней.
месяцев и следует избегать замораживания.



ХИМИЧЕСКАЯ СЕМЬЯ ОРГАЛА P 526:
*Акрилы,
*Акрилаты и метакрилаты,
*Винилы,
* Винилы и производные винила



ТИП ПРОДУКТА ORGAL P 526:
*Покрытие
*Технологии
*Готовые к использованию продукты
*Семейства продуктов
*Готовая к использованию продукция — краски и покрытия.
*Другие краски и покрытия



ОСОБЕННОСТИ И ПРЕИМУЩЕСТВА ORGAL P 526:
*Маркировка претензий
*Без формальдегида,
*Другие заявления о маркировке
*Приложения и использование
*Рынки
*Строительная конструкция



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ОРГАЛА П 526:
Общая информация
Химический состав: ВА/ВВ
Всего твердых веществ (% ±1): 55 ± 1
pH: 4,0–6,0
Вязкость по Брукфилду (мПас): 2000–5000
MFFT (°C): 11 ± 1
Тс (°С): 25
Внешний вид: Молочно-белая эмульсия.
Структура полимера: ВА/ВВ
Подробная информац��я

Внешний вид: Белая эмульсия/молочно-белая жидкость.
Содержание твердого вещества (% ±1): 49–51
pH: 4 - 6
Вязкость (Brookfield RVT 6/20, сП): 2000 – 5000
Плотность (25°С, г/см³) ± 0,01: 1,08
MFFT (°C): ~11
Тс (°С): ~24
Стабильность при хранении: Беречь от замерзания.
Вязкость по Брукфилду (мПа×с): 4000 ± 1500
Тип продукта: Винилы > Полимерные эмульсии винилацетата
Химический состав: Виниловая эмульсия сополимера VeoVa
Физическая форма: Жидкость



МЕРЫ ПЕРВОЙ ПОМОЩИ ОРГАЛА Р 526:
-Описание мер первой помощи.
*Общие советы:
Покажите этот паспорт безопасности материала лечащему врачу.
*При вдыхании:
После ингаляции:
Свежий воздух.
*При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промыть кожу с
вода/душ.
*В случае зрительного контакта:
После зрительного контакта:
Промойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.
*При проглатывании:
После глотания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.
-Указание на необходимость немедленной медицинской помощи и специального лечения.
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ ORGAL P 526:
-Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Закройте дренажи.
Соберите, свяжите и откачайте пролитую жидкость.
Соблюдайте возможные ограничения по материалам.
Возьмите в сухом виде.
Утилизируйте должным образом.
Очистите пораженное место.



МЕРЫ ПОЖАРОТУШЕНИЯ ORGAL P 526:
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Углекислый газ (CO2)
Мыло
Сухой порошок
*Неподходящие средства пожаротушения:
Для этого вещества/смеси не установлены ограничения по огнетушащим веществам.
-Дальнейшая информация:
Не допускайте попадания воды для пожаротушения в поверхностные воды или систему грунтовых вод.



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/ПЕРСОНАЛЬНАЯ ЗАЩИТА ORGAL P 526:
-Параметры управления:
--Ингредиенты с параметрами контроля на рабочем месте:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
*Защита глаз/лица:
Используйте средства защиты глаз.
Безопасные очки
*Защита тела:
защитная одежда
*Защита органов дыхания:
Рекомендуемый тип фильтра: Фильтр A
-Контроль воздействия на окружающую среду:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ORGAL P 526:
-Условия безопасного хранения, включая любые несовместимости:
*Условия хранения:
Плотно закрыто.
Сухой.



СТАБИЛЬНОСТЬ И РЕАКЦИОННАЯ СПОСОБНОСТЬ ORGAL P 526:
-Химическая стабильность:
Продукт химически стабилен при стандартных условиях окружающей среды (комнатная температура).
-Возможность опасных реакций:
Данные недоступны


ORGAL P 671
Orgal P 671 представляет собой эмульсию винил-акрилового сополимера высокой концентрации, не содержащую APEO.
Orgal P 671 также обладает очень хорошей стойкостью к истиранию и хорошей стойкостью к внешним воздействиям.


Химическое семейство: акрилаты, акрилаты и метакрилаты, винилы, винилы и производные винила.
Тип продукта: Акрилы и акриловые сополимеры > Винил-акрил
Химический состав: Винил-акриловый сополимер


Orgal P 671 представляет собой сополимер винилацетата и акрила.
Orgal P 671 представляет собой эмульсию винил-акрилового сополимера высокой концентрации, не содержащую APEO.
Orgal P 671 образует прозрачную, средней твердости и блестящую пленку при высыхании при температуре выше 10°C.


Orgal P 671 обладает превосходным связыванием пигментов, что обеспечивает очень высокую стойкость к истиранию даже при высоком уровне содержания ПВХ.
Orgal P 671 универсален и прост в приготовлении.
Orgal P 671 также обладает очень хорошей стойкостью к истиранию и хорошей стойкостью к внешним воздействиям.



ИСПОЛЬЗОВАНИЕ И ПРИМЕНЕНИЕ ORGAL P 671:
Orgal P 671 также обладает очень хорошей стойкостью к истиранию и хорошей стойкостью к внешним воздействиям.
Orgal P 671 используется для широкого спектра применений: для большинства внутренних покрытий, от гладких до полуглянцевых, текстурированных покрытий, грунтовок и штукатурок.



ХАРАКТЕРИСТИКИ ORGAL P 671:
*Штукатурка/Шпаклевка
*Отличный



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ОРГАЛА П 671:
Химический состав: Винил-акриловый сополимер
Всего твердых веществ (% ±1): 55
рН: 4,5 - 5,5
Вязкость по Брукфилду (мПас макс): 500
MFFT (°C): 10 ± 1
Тс (°С): 17
Внешний вид: Белая эмульсия
Структура полимера: ВА/АК
Тип продукта: Акрилы и акриловые сополимеры > Винил-акрил
Физическая форма: Жидкость



МЕРЫ ПЕРВОЙ ПОМОЩИ ORGAL P 671:
-Описание мер первой помощи.
*Общие советы:
Покажите этот паспорт безопасности материала лечащему врачу.
*При вдыхании:
После ингаляции:
Свежий воздух.
*При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промыть кожу с
вода/душ.
*В случае зрительного контакта:
После зрительного контакта:
Промойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.
*При проглатывании:
После глотания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.
-Указание на необходимость немедленной медицинской помощи и специального лечения.
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ ORGAL P 671:
-Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Закройте дренажи.
Соберите, свяжите и откачайте пролитую жидкость.
Соблюдайте возможные ограничения по материалам.
Возьмите в сухом виде.
Утилизируйте должным образом.
Очистите пораженное место.



МЕРЫ ПОЖАРОТУШЕНИЯ ORGAL P 671:
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Углекислый газ (CO2)
Мыло
Сухой порошок
*Неподходящие средства пожаротушения:
Для этого вещества/смеси не установлены ограничения по огнетушащим веществам.
-Дальнейшая информация:
Не допускайте попадания воды для пожаротушения в поверхностные воды или систему грунтовых вод.



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/ПЕРСОНАЛЬНАЯ ЗАЩИТА ORGAL P 671:
-Параметры управления:
--Ингредиенты с параметрами контроля на рабочем месте:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
*Защита глаз/лица:
Используйте средства защиты глаз.
Безопасные очки
*Защита тела:
защитная одежда
*Защита органов дыхания:
Рекомендуемый тип фильтра: Фильтр A
-Контроль воздействия на окружающую среду:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ORGAL P 671:
-Условия безопасного хранения, включая любые несовместимости:
*Условия хранения:
Плотно закрыто.
Сухой.



СТАБИЛЬНОСТЬ И РЕАКЦИОННАЯ СПОСОБНОСТЬ ORGAL P 671:
-Химическая стабильность:
Продукт химически стабилен при стандартных условиях окружающей среды (комнатная температура).
-Возможность опасных реакций:
Данные недоступны


ORGAL P 6820
Orgal P 6820 — это универсальная и простая в приготовлении эмульсия винилового сополимера, не содержащая APEO и аммиака, которая образует прозрачные, нелипкие и прочные пленки при высыхании при температуре выше 12°C.


Химическое семейство: акрилаты, акрилаты и метакрилаты, винилы, винилы и производные винила.
Тип продукта: Акрилы и акриловые сополимеры > Винил-акрил
Химический состав: Винилацетат/акрилат.


Orgal P 6820 представляет собой высокоэффективный, не содержащий APEO, не содержащий аммиака, простой в приготовлении сополимер винилацетата и акрилата, который образует прозрачные, нелипкие и прочные пленки при высыхании при температуре выше 12°C.
Orgal P 6820 обладает превосходной способностью связывать пигменты, что обеспечивает превосходную стойкость к истиранию даже при высоком уровне содержания ПВХ.


Orgal P 6820 обладает превосходной стойкостью к истиранию и воде, а также отличным образованием пленки и адгезией.
Orgal P 6820 рекомендуется для внутренних архитектурных красок и подходит для полуглянцевых красок яичной скорлупы.


Orgal P 6820 — это универсальная и простая в приготовлении эмульсия винилового сополимера, не содержащая APEO и аммиака, которая образует прозрачные, нелипкие и прочные пленки при высыхании при температуре выше 12°C.
Orgal P 6820 содержит эмульсию нового поколения с превосходной способностью связывания пигментов, которая обеспечивает превосходную стойкость к истиранию даже при высоком уровне содержания ПВХ.



ИСПОЛЬЗОВАНИЕ И ПРИМЕНЕНИЕ ORGAL P 6820:
Применение Orgal P 6820: Строительство — ограждающие конструкции, кровельные и архитектурные покрытия.
Orgal P 6820 обладает превосходной способностью связывать пигменты, что обеспечивает превосходную стойкость к истиранию даже при высоком уровне содержания ПВХ.

Orgal P 6820 обладает превосходной стойкостью к истиранию и воде, а также отличным образованием пленки и адгезией.
Orgal P 6820 рекомендуется для внутренних архитектурных красок и подходит для полуглянцевых красок яичной скорлупы.



ХИМИЧЕСКОЕ СЕМЕЙСТВО ORGAL P 6820:
*Акрилы, акрилаты и метакрилаты,
*Винилы, винилы и производные винила



ТИП ПРОДУКТА ORGAL P 6820:
*Покрытие
*Технологии
*Готовые к использованию продукты
*Семейства продуктов
*Готовая к использованию продукция — краски и покрытия.
*Другие краски и покрытия



ОСОБЕННОСТИ И ПРЕИМУЩЕСТВА ORGAL P 6820:
*Маркировка претензий
*Без формальдегида,
*Другие заявления о маркировке
*Приложения и использование
*Рынки
*Строительная конструкция



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ORGAL P 6820:
Внешний вид: Белая эмульсия
Твердое содержание (%_1): 55
Вязкость (Brookfield LVT 2/60): макс. 500 сП.
рН: 4,5 - 5,5
Плотность (25°С, г/см³): 1,08 ± 0,01.
MFFT (°C): 12
Тс (°С): 20
Стабильность при хранении: Беречь от замерзания.
Тип продукта: Акрилы и акриловые сополимеры > Винил-акрил
Химический состав: Винилацетат/акрилат.
Физическая форма: Эмульсия



МЕРЫ ПЕРВОЙ ПОМОЩИ ORGAL P 6820:
-Описание мер первой помощи.
*Общие советы:
Покажите этот паспорт безопасности материала лечащему врачу.
*При вдыхании:
После ингаляции:
Свежий воздух.
*При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промыть кожу с
вода/душ.
*В случае зрительного контакта:
После зрительного контакта:
Промойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.
*При проглатывании:
После глотания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.
-Указание на необходимость немедленной медицинской помощи и специального лечения.
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ ORGAL P 6820:
-Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Закройте дренажи.
Соберите, свяжите и откачайте пролитую жидкость.
Соблюдайте возможные ограничения по материалам.
Возьмите в сухом виде.
Утилизируйте должным образом.
Очистите пораженный участок.



МЕРЫ ПОЖАРОТУШЕНИЯ ORGAL P 6820:
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Углекислый газ (CO2)
Мыло
Сухой порошок
*Неподходящие средства пожаротушения:
Для этого вещества/смеси не установлены ограничения по огнетушащим веществам.
-Дальнейшая информация:
Не допускайте попадания воды для пожаротушения в поверхностные воды или систему грунтовых вод.



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/ПЕРСОНАЛЬНАЯ ЗАЩИТА ORGAL P 6820:
-Параметры управления:
--Ингредиенты с параметрами контроля на рабочем месте:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
*Защита глаз/лица:
Используйте средства защиты глаз.
Безопасные очки
*Защита тела:
защитная одежда
*Защита органов дыхания:
Рекомендуемый тип фильтра: Фильтр A
-Контроль воздействия на окружающую среду:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ORGAL P 6820:
-Условия безопасного хранения, включая любые несовместимости:
*Условия хранения:
Плотно закрыто.
Сухой.



СТАБИЛЬНОСТЬ И РЕАКЦИОННАЯ СПОСОБНОСТЬ ORGAL P 6820:
-Химическая стабильность:
Продукт химически стабилен при стандартных условиях окружающей среды (комнатная температура).
-Возможность опасных реакций:
Данные недоступны


ORGAL P 806 S
Orgal P 806 S Orgal P 806 S by Organik Kimya is a styrene acrylic copolymer. Orgal P 806 S is suitable for primers. Recommended for architectural exterior paints, textured paints, EIFS topcoats and elastomeric wall paints. It is in-line with VOC regulations, phasing out formaldehyde, ammonia and other restricted substances. Orgal P 806 S are water based polymers that can be produced from styrene and various acrylate esters such as methyl methacrylate, butyl acrylate, 2-ethylhexyl acrylate, acrylic acid, etc. By selecting the appropriate hard (ie styrene) and soft monomers, polymers with specific attributes for a variety of end-use applications can be built. Orgal P 806 S are versatile because of the building blocks and Tg that can be created. All of the different acrylic monomers can be used to build a random copolymer. Suppliers continue to develop new monomers for use by the synthetic emulsion polymers industry. Because of the wide variety of properties that can be achieved, Orgal P 806 S find use in every market where water-based systems are used. Resin-supported emulsions Resin-supported emulsions (RSE) are a unique subset of Orgal P 806 S. An emulsion is built on an alkali soluble resin that results in a vehicle with low MFFT relative to the polymers Tg. These products have much of the same flexibility and broad applicability as do Orgal P 806 S. Benefits: UV resistance Broad tensile/elongation balance Crosslinkable Good adhesion to common substrate Celanese manufactures Orgal P 806 S dispersions for use in a variety of industrial and consumer end-use applications, including: architectural decorative coatings such construction products as ceramic tile adhesives, fillers, putties and elastomeric roof coatings glass-fiber secondary binder applications, such as wall coverings Orgal P 806 S dispersions have a limited availability. Please check with your Celanese representative for current statuses. View specific products and product grades throughout our website as well. Orgal P 806 S is a water-based dispersion emulsion of styrene acrylic copolymer. It is a surfactant stabilized colloid free emulsion that has excellent pigment loading characteristics, alkali resistance, and good binding capacity to hold texture aggregates. This product is used for producing semi gloss to matt finish emulsion paint, interior and exterior architectural structure. Orgal P 806 S are used as binder for interior and exterior paints due to their outstanding pigment binding properties. Orgal P 806 S offer ideal gloss, film strength, durability and resistance to removal by detergents. Coatings based on styrene acrylate emulsions display excellent U.V stability and resistance to water, and alkalis. It is important to note that increasing the styrene content in styrene/acrylic copolymers may impair the water absorption and elasticity of the film. These coatings require very low maintenance as they have low tendency to pick up dirt and show good film flexibility and hardness. Orgal P 806 S are considered as a significant component of floor finishes. Majorly used in architectural/decorative paints for interior and exterior wall coatings, gloss paints for kitchen and bath, façades etc. followed by the wood and furniture industry. An aqueous coating composition comprising a mixture of: (i) an aqueous emulsion of a first polymeric film-forming resin; and (ii) a second polymeric film-forming resin comprising an organic solution of a plasticised Orgal P 806 S emulsified in water. An aqueous coating composition as claimed in claim 1, wherein the plasticised Orgal P 806 S is present in an amount of greater than or equal to 2 wt% and less than or equal to 15 wt%, preferably greater than or equal to 3 wt% and less than or equal to 7 wt% based on the total weight of the composition. An aqueous coating composition as claimed in claim 1 or 2, wherein the Orgal P 806 S is derivable by polymerisation of a monomer mixture comprising one or more alkyl (meth)acrylate monomers and one or more optionally substituted styrene comonomers. An aqueous coating composition as claimed in any one of the preceding claims, wherein the styrene-acrylic copolymer is derivable from a monomer mixture comprising greater than or equal to 30 wt% and less than or equal to 60 wt% of one or more alkyl (meth)acrylate comonomers and greater than or equal to 40 wt% and less than or equal to 70 wt% of one or more optionally substituted styrene comonomers. An aqueous coating composition as claimed in claim 3 or 4, wherein the one or more alkyl (meth)acrylates comprises one or more C1 to C8 alkyl (meth)acrylates. An aqueous coating composition as claimed in any one of claims 3 to 5, wherein the one or more optionally substituted styrene monomers are selected from one or more of unsubstituted styrene and C1 to C6 alkyl substituted styrene. An aqueous coating composition as claimed in any one of the preceding claims, wherein the Orgal P 806 S is essentially not cross-linked. An aqueous coating composition as claimed in any one of the preceding claims, wherein the Orgal P 806 S has a weight averaged molecular weight of greater than or equal to 50,000 Daltons. An aqueous coating composition as claimed in any one of the preceding claims, wherein the Orgal P 806 S has a weight averaged molecular weight of less than or equal to 200,000 Daltons. An aqueous coating composition as claimed in any one of the preceding claims, wherein the ratio by weight of the first polymeric film-forming resin to the plasticised Orgal P 806 S is 2:1 to 1:4. An aqueous coating composition as claimed in any one of the preceding claims, wherein the first polymeric film-forming resin is selected from an acrylic resin, a styrene-acrylic resin, a polyvinyl acetate resin, a polyurethane resin, an alkyd resin or a polyalkyl siloxane. An aqueous coating composition as claimed in any one of the preceding claims, wherein the first polymeric film-forming resin is an acrylic resin. An aqueous coating composition as claimed in any one of the preceding claims, wherein the first polymeric film-forming resin is a copolymer. An aqueous coating composition as claimed in any one of the preceding claims, wherein the first polymeric film-forming resin is present in an amount of 1 to 20% by weight, preferably 2 to 10% by weight, based on the total weight of the composition. An aqueous coating composition as claimed in any one of the preceding claims wherein the first polymeric film-forming resin is essentially a non-thickening polymeric resin. An aqueous coating composition as claimed in any one of the preceding claims further including a thickening agent. An aqueous coating composition as claimed in any one of the preceding claims wherein the first polymeric film-forming resin has a weight average molecular weight of greater than or equal to 225,000 Daltons and less than or equal to 600,000 Daltons. An aqueous coating composition as claimed in any one of the preceding claims wherein said coating composition further includes one or more pigments. An aqueous coating composition as claimed in any one of the preceding claims wherein said coating composition further includes one or more extenders. An aqueous coating composition as claimed in any one of the preceding claims, wherein the aqueous coating composition has a solids content of from 30 to 75 wt% based on the total weight of the composition. An aqueous coating composition as claimed in any one of the preceding claims, wherein the aqueous coating composition consists essentially of: (i) 1 to 20 wt% of the first polymeric film-forming resin; (ii) 2 to 15 wt% of the plasticised Orgal P 806 S; (iii) 5 to 25 wt% of one or more pigments; (iv) 30 to 60 wt% of one or more extenders; (v) 0.1 to 7 wt% of one or more thickeners; (vi) 0 to 6 wt% of one or more adjuvants selected from antibacterial agents, antifoaming agents, pH regulators, wetting agents and dry film protection agents; (vii) 3 to 8 wt% of an organic solvent; and (viii) water present in an amount of greater than or equal to 10 wt% based on the total weight of the aqueous coating composition, such that the sum of the percent by weight of each of the components (i) to (viii) totals 100% by weight. An aqueous coating composition as claimed in any one of the preceding claims, wherein the aqueous coating composition is in the form of a water based paint. Product Spectrum Product Name : Orgal P 806 S Chemical Composition of Orgal P 806 S: AC Total Solids of Orgal P 806 S(%±1) : 60 pH of Orgal P 806 S: 5.0-5.0 Viscosity of Orgal P 806 S(mPa.s max) : 2,000 MFFT of Orgal P 806 S(°C) : <0 Tg of Orgal P 806 S(°C) : -35 Application Areas of Orgal P 806 S Anticarbonation Coatings : Suitable Elastomeric Wall Coatings : Excellent Textured Coatings : Excellent Orgal P 806 S Technical Datasheet Orgal P 806 Sis a high solids, APEO-free acrylic polymer produced with UV crosslinking technology. Orgal P 806 Sis used to formulate elastomeric wall coatings having outstanding exterior durability, excellent elongation, tensile strength, crack bridging properties and dirt pick-up resistance. The grade does not turn yellow on UV exposure and exhibits crack resistance, very low water absorption, water vapor permeability, very low surface tack. Orgal P 806 Sshows adhesion over a variety of substrates. Orgal P 806 Sis internally plasticized which eliminates the need for external plasticizer. Orgal P 806 Shas a shelf life of 12 months. Product Type of Orgal P 806 SAcrylics & Acrylic Copolymers Chemical Composition of Orgal P 806 SAcrylic polymer Physical Form of Orgal P 806 SLiquid Architectural Coatings of Orgal P 806 S A broad range of all acrylics, styrene acrylics and vinyl acrylics for matt, semi-gloss and gloss interior and exterior paints. All new product developments are in line with the latest VOC regulations, phasing out formaldehyde, ammonia and other restricted substances. Orgal P 806 S Chemical Composition of Orgal P 806 S:AC Total Solids of Orgal P 806 S(%±1): 60 pH of Orgal P 806 S: 5.0 - 7.0 Viscosity of Orgal P 806 S(mPa.s, max) : 2,000 MFFT of Orgal P 806 S(°C): <0 Tg of Orgal P 806 S(°C): -35 In summary, the main features of the Orgal P 806 Sare as follows. • Orgal P 806 Sis a styrene acrylic polymer without APEO and without ammonia. • Orgal P 806 Soffers excellent interaction with various PU rheology organizers, • Orgal P 806 Sgives perfect color intensity with different dye systems, • Orgal P 806 Shas excellent adhesion to pigments and excellent resistance to friction, • Orgal P 806 Soffers very good adhesion on mineral surfaces, • Orgal P 806 Shas excellent water resistance, • Orgal P 806 Shas a low viscosity which facilitates the use in production facilities. Orgal P 806 S, which is the product of long-term studies on innovation and the use of new technologies, is an excellent choice for high quality paints as ammonia-free styrene acrylic polymer with reduced environmental effects. A method of preparing an aqueous coating composition as defined in any one of the preceding claims comprising contacting, preferably mixing, an aqueous emulsion of a first polymeric film-forming resin as defined in any one of the preceding claims with an organic solution of a plasticised Orgal P 806 S emulsified in water as defined in any one of the preceding claims. Suitably, the first polymeric film-forming resin as defined hereinafter is a conventional film-forming polymer resin, such as a vinylic or acrylic resin, employed in emulsion paints. Unexpectedly, it has been found that the inclusion of a second polymeric film-forming resin comprising an organic solution of a plasticised Orgal P 806 S emulsified in water in combination with an aqueous emulsion of the first polymeric film-forming resin typically provides an aqueous coating composition which exhibits improved adhesion and cohesion compared with a comparable aqueous coating composition which only includes either the first polymeric film-forming resin or the second polymeric film-forming resin. Suitably, the aqueous coating composition of the present invention may exhibit improved UV colour fastness, improved abrasion resistance and improved water resistance (i.e. scrub resistance) compared with waterborne counterpart compositions which include either the first polymeric film-forming resin or the second polymeric film-forming resin only. By the term "aqueous emulsion of a first polymeric film-forming resin" we mean the first film-forming resin is insoluble in water and is in the form of an aqueous colloidal dispersion. The second film-forming resin is dissolved in an organic solvent which is immiscible with water and the resultant organic solution emulsified in water. Preferably, the second film-forming resin is essentially an organic solution-in-water emulsion wherein the water is the predominant phase. Suitably, the aqueous coating compositions of the present invention are water based and so the main liquid component is water. Conventional emulsion paints usually comprise, as well as water, a minor amount of an organic solvent, such as 2,2,4-trimethyl 1,3-pentanediol monoisobutyrate (Texanol™), Butyl Cellosolve™, or white spirit, to aid coalescence of the dispersed film - forming polymer. Preferably, the aqueous coating composition of the present invention includes less than or equal to 10 wt%, more preferably less than or equal to 8 wt%, even more preferably less than or equal to 5 wt%, even more preferably less than or equal to 3 wt%, based on the total weight of the aqueous coating composition, of organic solvents. Preferably, all of the organic solvent present in the aqueous coating composition is derived from the organic solvent-in-water emulsion of the plasticised Orgal P 806 S. Preferably, the aqueous composition of the present invention comprises greater than or equal to 10 wt%, more preferably greater than or equal to 15 wt%, even more preferably greater than or equal to 20 wt%, most preferably greater than or equal to 25 wt%, based on that total weight of the composition of water. Preferably, the aqueous composition of the present invention comprises less than or equal to 55 wt%, more preferably less than or equal to 45 wt%, even more preferably less than or equal to 35 wt%, most preferably less than or equal to 30 wt%, based on the total weight of the compositions, of water. It will be appreciated the organic solvent of the second film-forming resin forms the balance of the liquid phase of the aqueous coating composition of the present invention. Preferably, the plasticised Orgal P 806 S comprises less than or equal to 5 wt%, more preferably less than or equal to 3 wt%, most preferably less than or equal to 1 wt%, based on weight averaged molecular weight of the Orgal P 806 S, of one or more cross-linking comonomers. Most preferably, the Orgal P 806 S is non-crosslinked. Preferably, the plasticised Orgal P 806 S includes essentially no functional groups which may react with complimentary functional groups present in the first polymeric film-forming resin. Suitably, the resultant film formed from the aqueous coating composition is essentially non-crosslinked. The Orgal P 806 S is essentially a linear polymer. Preferably, the plasticised Orgal P 806 S itself (i.e. the Orgal P 806 S and plasticiser but not including the organic solvent and aqueous phase) is present in an amount of greater than or equal to 2 wt%, more preferably greater than or equal to 3 wt%, most preferably greater than or equal to 4 wt%, based on the total weight of the aqueous coating composition. Preferably, the plasticised Orgal P 806 S itself (i.e. the Orgal P 806 S and plasticiser but not including the organic solvent and aqueous phase) is present in an amount of less than or equal to 15 wt%, more preferably less than or equal to 10 wt%, most preferably less than or equal to 7 wt%, based on the total weight of the aqueous coating composition. The second polymeric film-forming resin comprising the Orgal P 806 S and plasticiser, and other non-aqueous soluble components if present, dissolved in an organic solvent, such as C9-C11 aliphatic hydrocarbons and the resultant organic solution is emulsified in an aqueous phase. It will be appreciated by those skilled in the art that it is necessary to include the appropriate amount of such an organic solvent-in-water emulsion so that the overall content of the Orgal P 806 S itself, organic solvent and plasticiser, in the aqueous coating composition of the present invention falls within the preferred limits as defined herein. Suitably, such amounts may be determined by routine experimentation based on the known concentration of Orgal P 806 S, and organic solvent and plasticiser if present, in the Orgal P 806 S aqueous mixture. Although the Orgal P 806 S and plasticiser is in the form of an organic solvent-in-water emulsion, the Orgal P 806 S is essentially insoluble in water. The Orgal P 806 S is essentially formed from hydrophobic monomers as detailed hereinafter which typically have a solubility in water of less than 50 g/l at 25 °C and 1 bar. Preferably, the Orgal P 806 S itself is present in an amount of greater than or equal to 10 wt% and less than or equal to 35 wt%, most preferably approximately 20 wt%, based on the total weight of the organic solution emulsified in water. Suitably, the organic solution of the Orgal P 806 S emulsified in water comprises less than or equal to 65 wt% and greater than or equal to 35 wt%, most preferably approximately 45 wt% of water. Suitably, the organic solution of the Orgal P 806 S emulsified in water comprises between 5 to 20 wt%, most preferably 15 wt% of an organic solvent. Suitably, the organic solution of the Orgal P 806 S emulsified in water comprises between 5 to 30 wt%, most preferably approximately 20 wt% of a plasticiser, based on the total weight of the organic solution emulsified in water. Suitable organic solvents are well known to those skilled in the art and include 2,2,4-trimethyl-1,3-peritanediol monoisobutyrate (Texanol™), Butyl Cellosolve™ and white spirit. Suitably, when the Orgal P 806 S is in the form of an aqueous mixture as defined herein, the aqueous mixture comprising 20 wt% of the Orgal P 806 S, 20% plasticiser, 45 wt% water and 15 wt% organic solvent has a Brookfield viscosity of (spindle number 1 at 60 rpm and at 25 °C) of greater than or equal to 30 cps and less than or equal to 60 cps, more preferably greater than or equal to 40 cps and less than or equal to 50 cps. Preferably, the Orgal P 806 S is formed by polymerisation of a monomer mixture comprising one or more acrylic monomers as defined herein with one or more optionally substituted styrene monomers as defined herein. Preferred acrylic monomers include acrylic acid, methacrylic acid and the esters of such acids. Preferred esters include alkyl (meth)acrylates which term refers to the corresponding acrylate or methacrylate ester which are usually formed from the corresponding acrylic or methacrylic acids by reaction with an alkanol. In other words the term "alkyl (meth)acrylate" refers to either an alkyl methacrylate or an alkyl acrylate. Other acrylic monomers include hydroxyl functional monomers such as hydroxyethyl acrylate, hydroxyethyl methacrylate and hydroxybutyl acrylate and gamine functional monomers such as dimethylaminoethyl methacrylate. Preferably, the Orgal P 806 S includes less than or equal to 10 wt%, more preferably less than or equal to 5 wt%, most preferably essentially no hydroxy and/or amine functional acrylic monomers. Preferably, the alkyl (meth)acrylate is a (C1-C22)alkyl (meth)acrylate. Examples of C1-C22 alkyl groups of the alkyl (meth)acrylates includes methyl, ethyl, n-propyl, n-butyl, iso-butyl, tert-butyl, iso-propyl, pentyl, hexyl, cyclohexyl, 2-ethyl hexyl, heptyl, octyl, ethylhexyl, nonyl, decyl, isodecyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl, behenyl, and isomers thereof. When there are sufficient number of carbon atoms, the alkyl group may be straight or branched chain. Preferably, the (C1-C22)alkyl (meth)acrylate is a (C1-C8)alkyl methacrylate, in particular methyl methacrylate, ethyl acrylate, butyl acrylate, butyl methacrylate and 2-ethylhexyl acrylate, and isomers thereof. Preferably, the Orgal P 806 S is derived from a monomer mixture comprising two or more alkyl (meth)acrylate monomers as defined herein, in particular butyl methacrylate, especially iso-butyl methacrylate, and 2-ethylhexyl acrylate. Preferably, the Orgal P 806 S includes less than or equal to 10 wt%, based on the weight average molecular weight of the Orgal P 806 S, more preferably less than or equal to 5 wt%, most preferably essentially no acrylic acid monomers. Preferably, the Orgal P 806 S includes less than or equal to 10 wt%, based on the weight average molecular weight of the Orgal P 806 S, more preferably less than or equal to 5 wt%, most preferably essentially no methacrylic acid monomers. Highly preferred acrylic monomers consist essentially of one or more alkyl (meth)acrylate monomers as defined herein. Preferably, the Orgal P 806 S comprises greater than or equal to 30 wt%, more preferably greater than or equal to 40 wt%, most preferably greater than or equal to 45 wt%, based on the weight average molecular weight of the Orgal P 806 S, of one or more acrylic monomers as defined herein. Preferably, the Orgal P 806 S comprises less than or equal to 60 wt% more preferably less than or equal to 55 wt%, most preferably less than or equal to 50 wt%, based on the weight average molecular weight of the Orgal P 806 S, of one or more acrylic monomers as defined herein. Preferred optionally substituted styrene monomers include unsubstituted styrene and styrene substituted with one or more C1-C6 alkyl substituents. The styrene may be substituted at the α or β position of the ethylene group or on the aromatic ring, or at a combination of these positions. Preferably, the styrene is substituted at the α or β position of the ethylene group. More preferred optionally substituted styrene monomers include unsubstituted styrene and styrene substituted with one or more C1-C6 alkyl substituents, such as methyl, ethyl, propyl, butyl, pentyl or hexyl which alkyl group when there are sufficient number of carbon atoms may be straight or branched chain. Highly preferred optionally substituted styrene monomers include unsubstituted styrene and mono substituted C1-C6 alkyl styrene, particularly mono substituted C1-C4alkyl styrene such as butyl styrene. Preferably, the Orgal P 806 S comprises greater than or equal to 40 wt%, more preferably greater than or equal to 45 wt%, most preferably greater than or equal to 50 wt%, based on the weight average molecular weight of the Orgal P 806 S, of one or more optionally substituted styrene monomers as defined herein. Preferably, the Orgal P 806 S comprises less than or equal to 70 wt%, more preferably less than or equal to 60 wt%, most preferably less than or equal to 55 wt%, based on the weight average molecular weight of the Orgal P 806 S, of one or more optionally substituted styrene monomers as defined herein. Preferably, the Orgal P 806 S is derived essentially from a monomer mixture comprising one or more alkyl (meth)acrylate monomers a defined herein and one or more optionally substituted styrene comonomers as defined herein. In other words, the alkyl (meth)acrylate and optionally substituted styrene monomers represent greater than 99%, preferably 100%, of the monomers present in the Orgal P 806 S. Suitable plasticisers are well known to those skilled in the art and include phthalic anhydride esters, trimellitic acid esters, hydrogenated terphenyls, chlorinated parrafins as disclosed in US 5,962,579 . Preferably, the one or more plasticisers comprises a chloroparaffin or an alkyl phthalate. The plasticiser may be present in an amount of greater than or equal to 70 wt% and less than or equal to 20 wt%, most preferably 50 wt%, based on the weight averaged molecular weight of the Orgal P 806 S. Preferably, the Orgal P 806 S includes less than 5 wt%, more preferably less than 3 wt%, most preferably less than 2 wt%, of one or more adjuvants, such as in can preservation agents i.e. methyl iso-thiazolinone or chloro methyl isothiazolinone. Preferably, the Orgal P 806 S itself has a weight averaged molecular weight of greater than or equal to 30,000, more preferably greater than or equal to 50,000, most preferably greater than or equal to 70,000. Preferably, the Orgal P 806 S itself (i.e. in the absence of any plasticiser and further adjuvants as defined herein) has a weight averaged molecular weight of less than or equal to 400,000, more preferably less than or equal to 200,000, most preferably less than or equal to 100,000. Preferably, the Orgal P 806 S itself (i.e. in the absence of any plasticiser and further adjuvants as defined herein) has a glass transition temperature (Tg) of less than or equal to 70 °C and greater than or equal to 35 °C. Preferably, the glass transition temperature of the Orgal P 806 S and plasticiser is less than or equal to 50 °C and greater than or equal to -10 °C, preferably greater than or equal to 0 °C. Glass transition temperatures may be determined by routine experimentation using the Fox equation, employing a pre-dried (at 105 °C for 2 hours) sample of the Orgal P 806 S, with a heating rate of 4 °C min-1 over a temperature range of -60 to +150 °C and a modulation rate of ±1 °C per 55 sec. Characteristics: Good film forming Good binding Plasticizer free Solvent free Excellent resistance towards alkalis and water Excellent pigment / extender wetting properties Specifications: Solid content 50.0 +/- 1.0% pH 7.0 - 8.0 Viscosity 1500 - 6000 mPa.s Dispersion properties: Appearance White, viscous emulsion Emulsifying system Anionic (biodegradable) Tg + 18 ° C Particle size approx. 140 nm Film properties: Appearance Clear, glossy and transparent Surface Non tacky MFFT + 17 ° C Applications: Orgal P 806 S can be used for interior and exterior paints with good washability, it is also suitable for the formulation of floor tile and building adhesives, roof coatings and sealants. Storage: In shade of the sun and at temperatures between + 5 ° C and + 30 ° C Shelf life: 6 months in original closed packaging
ORGAL P 838 W
Orgal P 838 W совместим с алкидами и обеспечивает прозрачность при нанесении морилок на дерево.


Тип продукта: Акрилы и акриловые сополимеры
Химический состав: Акриловый полимер.


Orgal P 838 W — акриловый полимер, не содержащий APEO и формальдегида, разработанный для высокоэффективных покрытий для различных наружных и внутренних работ, покрытий по дереву, морилок.
Orgal P 838 W совместим с алкидами и обеспечивает прозрачность при нанесении морилок на дерево.


Максимальный срок хранения Orgal P 838 W составляет 12 месяцев.
При использовании в покрытиях на водной основе Orgal P 838 W демонстрирует адгезию в мокром и сухом виде, превосходную внешнюю долговечность, стойкость к растрескиванию, мелу и щелочам, сохранение блеска и оттенка, а также отличную реакцию на модификаторы реологии.



ИСПОЛЬЗОВАНИЕ И ПРИМЕНЕНИЕ ORGAL P 838 W:
Области применения Orgal P 838 W: модификатор цемента, базовые покрытия EIFS и полы из терраццо.
При использовании в покрытиях на водной основе Orgal P 838 W демонстрирует адгезию в мокром и сухом виде, превосходную внешнюю долговечность, стойкость к растрескиванию, мелу и щелочам, сохранение блеска и оттенка, а также отличную реакцию на модификаторы реологии.


Orgal P 838 W совместим с алкидами и обеспечивает прозрачность при нанесении морилок на дерево.
Orgal P 838 W используется в клеях, герметиках, красках и покрытиях.
Области применения Orgal P 838 W: краски для дома, полуглянцевые краски из яичной скорлупы, фасадные краски, глянцевые краски, краски для внутренних работ, краски для кухни и ванной комнаты, морилки для дерева.



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ORGAL P 838 W:
Химический состав: переменный ток
Всего твердых веществ (% ±1): 46
pH: 7,5 – 8,5
Вязкость по Брукфилду (мПас макс): 500
MFFT (°C): 14 ± 1
Tg (°C): н/д
Внешний вид: Опалово-белая эмульсия.
Структура полимера: переменный ток
Продукт 2: ORGAL P 838 W

Химический состав: Акриловый полимер.
Всего твердых веществ (% ±1): 46
рН: 7,5
Вязкость (мПа.с макс): 500
MFFT (°C): 14
Тс (°С): 21
Тип продукта: Акрилы и акриловые сополимеры
Физическая форма: Эмульсия



МЕРЫ ПЕРВОЙ ПОМОЩИ ORGAL P 838 W:
-Описание мер первой помощи.
*Общие советы:
Покажите этот паспорт безопасности материала лечащему врачу.
*При вдыхании:
После ингаляции:
Свежий воздух.
*При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промыть кожу с
вода/душ.
*В случае зрительного контакта:
После зрительного контакта:
Промойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.
*При проглатывании:
После глотания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.
-Указание на необходимость немедленной медицинской помощи и специального лечения.
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ ORGAL P 838 W:
-Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Закройте дренажи.
Соберите, свяжите и откачайте пролитую жидкость.
Соблюдайте возможные ограничения по материалам.
Возьмите в сухом виде.
Утилизируйте должным образом.
Очистите пораженный участок.



МЕРЫ ПОЖАРОТУШЕНИЯ ORGAL P 838 W:
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Углекислый газ (CO2)
Мыло
Сухой порошок
*Неподходящие средства пожаротушения:
Для этого вещества/смеси не установлены ограничения по огнетушащим веществам.
-Дальнейшая информация:
Не допускайте попадания воды для пожаротушения в поверхностные воды или систему грунтовых вод.



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/ПЕРСОНАЛЬНАЯ ЗАЩИТА ORGAL P 838 W:
-Параметры управления:
--Ингредиенты с параметрами контроля на рабочем месте:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
*Защита глаз/лица:
Используйте средства защиты глаз.
Безопасные очки
*Защита тела:
защитная одежда
*Защита органов дыхания:
Рекомендуемый тип фильтра: Фильтр A
-Контроль воздействия на окружающую среду:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ORGAL P 838 W:
-Условия безопасного хранения, включая любые несовместимости:
*Условия хранения:
Плотно закрыто.
Сухой.



СТАБИЛЬНОСТЬ И РЕАКЦИОННАЯ СПОСОБНОСТЬ ORGAL P 838 W:
-Химическая стабильность:
Продукт химически стабилен при стандартных условиях окружающей среды (комнатная температура).
-Возможность опасных реакций:
Данные недоступны


ORGAL P 838 W
Orgal P 838 W совместим с алкидами и обеспечивает прозрачность при нанесении морилок на дерево.


Тип продукта: Акрилы и акриловые сополимеры
Химический состав: Акриловый полимер.


Orgal P 838 W — акриловый полимер, не содержащий APEO и формальдегида, разработанный для высокоэффективных покрытий для различных наружных и внутренних работ, покрытий по дереву, морилок.
Orgal P 838 W совместим с алкидами и обеспечивает прозрачность при нанесении морилок на дерево.


Максимальный срок хранения Orgal P 838 W составляет 12 месяцев.
При использовании в покрытиях на водной основе Orgal P 838 W демонстрирует адгезию в мокром и сухом виде, превосходную внешнюю долговечность, стойкость к растрескиванию, мелу и щелочам, сохранение блеска и оттенка, а также отличную реакцию на модификаторы реологии.



ИСПОЛЬЗОВАНИЕ И ПРИМЕНЕНИЕ ORGAL P 838 W:
Области применения Orgal P 838 W: модификатор цемента, базовые покрытия EIFS и полы из терраццо.
При использовании в покрытиях на водной основе Orgal P 838 W демонстрирует адгезию в мокром и сухом виде, превосходную внешнюю долговечность, стойкость к растрескиванию, мелу и щелочам, сохранение блеска и оттенка, а также отличную реакцию на модификаторы реологии.


Orgal P 838 W совместим с алкидами и обеспечивает прозрачность при нанесении морилок на дерево.
Orgal P 838 W используется в клеях, герметиках, красках и покрытиях.
Области применения Orgal P 838 W: краски для дома, полуглянцевые краски из яичной скорлупы, фасадные краски, глянцевые краски, краски для внутренних работ, краски для кухни и ванной комнаты, морилки для дерева.



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ORGAL P 838 W:
Химический состав: переменный ток
Всего твердых веществ (% ±1): 46
pH: 7,5 – 8,5
Вязкость по Брукфилду (мПас макс): 500
MFFT (°C): 14 ± 1
Tg (°C): н/д
Внешний вид: Опалово-белая эмульсия.
Структура полимера: переменный ток
Продукт 2: ORGAL P 838 W

Хими��еский состав: Акриловый полимер.
Всего твердых веществ (% ±1): 46
рН: 7,5
Вязкость (мПа.с макс): 500
MFFT (°C): 14
Тс (°С): 21
Тип продукта: Акрилы и акриловые сополимеры
Физическая форма: Эмульсия



МЕРЫ ПЕРВОЙ ПОМОЩИ ORGAL P 838 W:
-Описание мер первой помощи.
*Общие советы:
Покажите этот паспорт безопасности материала лечащему врачу.
*При вдыхании:
После ингаляции:
Свежий воздух.
*При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промыть кожу с
вода/душ.
*В случае зрительного контакта:
После зрительного контакта:
Промойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.
*При проглатывании:
После глотания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.
-Указание на необходимость немедленной медицинской помощи и специального лечения.
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ ORGAL P 838 W:
-Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Закройте дренажи.
Соберите, свяжите и откачайте пролитую жидкость.
Соблюдайте возможные ограничения по материалам.
Возьмите в сухом виде.
Утилизируйте должным образом.
Очистите пораженный участок.



МЕРЫ ПОЖАРОТУШЕНИЯ ORGAL P 838 W:
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Углекислый газ (CO2)
Мыло
Сухой порошок
*Неподходящие средства пожаротушения:
Для этого вещества/смеси не установлены ограничения по огнетушащим веществам.
-Дальнейшая информация:
Не допускайте попадания воды для пожаротушения в поверхностные воды или систему грунтовых вод.



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/ПЕРСОНАЛЬНАЯ ЗАЩИТА ORGAL P 838 W:
-Параметры управления:
--Ингредиенты с параметрами контроля на рабочем месте:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
*Защита глаз/лица:
Используйте средства защиты глаз.
Безопасные очки
*Защита тела:
защитная одежда
*Защита органов дыхания:
Рекомендуемый тип фильтра: Фильтр A
-Контроль воздействия на окружающую среду:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ORGAL P 838 W:
-Условия безопасного хранения, включая любые несовместимости:
*Условия хранения:
Плотно закрыто.
Сухой.



СТАБИЛЬНОСТЬ И РЕАКЦИОННАЯ СПОСОБНОСТЬ ORGAL P 838 W:
-Химическая стабильность:
Продукт химически стабилен при стандартных условиях окружающей среды (комнатная температура).
-Возможность опасных реакций:
Данные недоступны


ORGAL P 839 W
Orgal p 839 w и акриловый полимер, не содержащий формальдегида, предназначены для высокоэффективных покрытий для различных наружных и внутренних применений, покрытий для дерева, морилок для дерева.
При использовании в Orgal p 839 w он демонстрирует адгезию во влажном и сухом состоянии, отличную внешнюю прочность, стойкость к растрескиванию, мелу и щелочам, сохранение блеска и оттенка, а также отличную реакцию модификатора реологии.
Тщательно разработанные механические свойства Orgal p 839 w улучшают стойкость к холодной проверке.

Акриловый полимер, не содержащий формальдегида, относится к типу акрилового полимера, который производится без использования формальдегида или содержит минимальные уровни формальдегида в составе своего состава.
Orgal p 839 w - это химическое соединение, которое традиционно используется в производстве некоторых смол и полимеров, но также известно своей потенциальной опасностью для здоровья.
Акриловая основа ORGAL P 839 W обеспечивает превосходную внешнюю прочность.
Orgal p 839 w демонстрирует совместимость с алкидами и прозрачность в банке в морилках для дерева.

Orgal p 839 w имеет максимальный срок хранения 12 месяцев.
Orgal p 839 w - отличный выбор для деревянных покрытий своими руками, а также красок на минеральных поверхностях.
Orgal p 839 w позволяет достичь очень низких показателей водопроницаемости в соответствии с EN 927-5.

Orgal p 839 w , образует прозрачную, среднетвердую и глянцевую пленку при сушке выше 10°C.
Orgal p 839 w обладает превосходным связыванием пигментов, что обеспечивает очень высокую стойкость к истиранию даже при высоком содержании ПВХ.
Orgal p 839 w представляет собой сополимер винилацетата и акрила.

Orgal p 839 w представляет собой тип сополимера, который содержит в своей молекулярной структуре как винилацетат, так и акриловые мономерные единицы.
Orgal p 839 w универсален и прост в составлении.
Orgal p 839 w также обладает очень хорошей устойчивостью к истиранию и хорошей долговечностью на открытом воздухе.

Orgal p 839 w используется для широкого спектра применений, для большинства внутренних покрытий от плоских до полуглянцевых, текстурированных покрытий, грунтовок и штукатурок.
Orgal p 839 w - это стирол-акриловый сополимер, специально разработанный для использования в красках для внутренних и наружных работ, не содержащих растворителей, матовых или полуглянцевых красок для стен со слабым запахом.
Orgal p 839 w не содержит летучих органических соединений, APEO, аммиака и формальдегида.

Orgal p 839 w устойчив к жидкому стеклу и может использоваться в составах силикатных красок.
Orgal p 839 w обеспечивает отличное пленкообразование без использования коалесцирующих агентов.
Краски на основе Orgal p 839 w демонстрируют отличную стойкость к влажному истиранию, щелочам и грязеобразованию при высоком диапазоне ПВХ, а также высокую способность связывать пигменты.

Orgal p 839 w обычно используется в рецептуре клеев.
Они обеспечивают склеивающие свойства, необходимые для адгезии без использования формальдегида.
В лакокрасочной промышленности Orgal p 839 w используется для создания пленок, которые хорошо прилипают к поверхностям, обеспечивают долговечность и демонстрируют низкий уровень выбросов летучих органических соединений.

Orgal p 839 w также может использоваться в текстильной промышленности, в частности, в производстве покрытий для тканей, обеспечивая такие свойства, как водоотталкивающие свойства и устойчивость к пятнам.
Orgal p 839 w может использоваться в рецептуре герметиков для воздуховодов отопления, вентиляции и кондиционирования воздуха (HVAC), способствуя общей эффективности и безопасности систем отопления, вентиляции и кондиционирования воздуха.

Химический состав / Общее содержание твердых веществ (%±1) / pH / Вязкость (мПа.с, макс.) / MFFT (°C) / Tg (°C):
Orgal P 74 S:
S/AC 50 7,0 - 8,0 3000 <3 5
Orgal Duraflex 84 S:
AC 50 7,0 - 8,0 1000 5 н/д
Orgal P 086VR:
AC 43 8,5 - 9,0 400 14 н/д
Orgal P 6830:
VA / AC 55 4,5 - 5,5 750 12 20
Orgal PST 5010:
С/С 50 7,5 - 9,0 2,000 11 11
Orgal PST 100 E:
S / AC 50 7,5 - 9,0 1 500 20 20
Оргал PST 100:
S / AC 50 7,5 - 9,0 1 500 20 20
Orgal PST 50 E:
/АМ 50 7,5 - 9,0 7,000 18 18
Orgal P 806 S:
С/Ас 50 7,5 - 9,0 8 000 <0 -6
Orgal P 056V:
S/AC 50 8,0 - 9,0 3 000 <3 5
Orgal K 6459 E:
AC 55 7,5 - 8,5 1 000 <0 -35
Orgal K 6455 E:
AC 60 5,0 - 7,0 2 000 <0 -35
Orgal PR 9464:
AC 46 8,5 - 9,0 500 <7 <3
Orgal PR 845 A:
AC 46,5 8,0 - 9,0 400 3 -1
Orgal PR 842 A:
AC 43 8,0 - 8,5 100 9 12
Orgal P 888:
AC 45 7,0 - 8,0 500 24 30
Orgal P 878:
AC 46 8,0 - 9,0 500 14 21
Orgal P 850 RR:
AC 50 8,0 - 9,0 1 000 18 22
Orgal P 850:
AC 50 8,5 - 9,5 400 18 22
Orgal P 838 W:
AC 46 7,5 - 8,5 500 14 н/д
Orgal P 8266:
AC 60 7,5 - 8,5 2 000 3 8
Orgal P 8240:
AC 43 7,5 - 8,5 400 14 н/д
Orgal P 826:
AC 60 8,5 - 9,5 6 000 5 9
Orgal P 808:
AC 50 7,0 - 8,0 750 5 8
Orgal P 050G:
AC 47 8,0 - 8,5 1 000 <3 н/д
Orgal P 036V:
AC 50 8,0 - 9,0 500 <3 0
Orgal P 6820:
VA / AC 55 4,5 - 5,5 500 12 20
Orgal P 671:
VA / AC 55 4,5 - 5,5 500 10 17
Orgal P 653:
VA / AC 58 4,0 - 6,0 5 000 10 20
Orgal P 600:
VA / AC 50 4,0 - 5,0 5 000 7 14
Orgal P 062 V:
VA / AC 53 4,0 - 5,5 4 000 <3 11
Orgal P 526:
VA / VeoVA 55 4,0 - 6,0 5,500 11 25
Orgal P 523 В:
VA / VeoVA 50 4,0 - 6,0 5 000 3 11
Orgal PST 50 A:
С/С 50 7,5 - 9,0 11 000 20 20

Orgal p 839 w используется в производстве клеев для ковровых основ и напольных покрытий.
Это помогает гарантировать, что в помещениях, где обычно используются эти материалы, снижается уровень выбросов формальдегида.
Orgal p 839 w находит применение в рецептурах деревянных покрытий и отделок для мебели и столярных изделий.

Эти покрытия обеспечивают защиту, улучшают эстетику и способствуют более безопасной среде в помещении.
Orgal p 839 w может быть включен в покрытия для бумажных и картонных изделий, обеспечивая улучшенные печатные свойства, влагостойкость и общую долговечность.
Orgal p 839 w используется в рецептуре герметиков для строительных применений.

Эти герметики обеспечивают адгезионные свойства и гибкость, избегая при этом потенциальных проблем со здоровьем, связанных с выделением формальдегида.
В кожевенной промышленности Orgal p 839 w может применяться в производстве покрытий для кожгалантереи, обеспечивающих защитные и эстетические свойства без использования формальдегида.
Orgal p 839 w может функционировать в качестве модификаторов реологии в различных составах.

Эти модификаторы влияют на вязкость и текучесть материала, влияя на его применение и эксплуатационные характеристики.
В соответствии с устойчивыми и экологически чистыми практиками, некоторые Orgal p 839 w разработаны как биоразлагаемые, что позволяет решить проблемы воздействия на окружающую среду определенных химических веществ.
Orgal p 839 w широко используется в производстве полимерных эмульсий.

Эти эмульсии находят применение в широком спектре отраслей промышленности, включая краски, покрытия и клеи.
Orgal p 839 w обычно используется в рецептуре герметиков и швов для проектов строительства и благоустройства дома.
Эти продукты способствуют герметизации и отделке без введения формальдегида.

Использует:
Orgal p 839 w используется в рецептуре клеев для различных применений, включая деревообработку, строительство и упаковку.
Эти клеи обеспечивают адгезивные свойства без использования формальдегида.
Orgal p 839 w используется в производстве покрытий и красок для таких поверхностей, как стены, мебель и автомобильные компоненты.

Они способствуют созданию долговечной отделки с меньшим воздействием на окружающую среду.
Эти полимеры, содержащиеся в строительных герметиках и герметиках, обеспечивают эффективную герметизацию без необходимости использования формальдегида.
Они обычно используются в таких областях, как установка окон, стыков и зазоров.

Orgal p 839 w используется в текстильной промышленности для создания отделки тканей, обеспечивая такие свойства, как водоотталкивающие свойства, устойчивость к морщинам и огнестойкость без включения формальдегида.
Применяется в покрытии бумаги и картона для улучшения таких свойств, как пригодность к печати, влагостойкость и общая долговечность, не способствуя выделению формальдегида.

Orgal p 839 w используется в составах клеев для напольных покрытий, в том числе для укладки ковровых покрытий и плиточных клеев, где требуется прочное сцепление без присутствия формальдегида.
Orgal p 839 w используется в отделке древесины и морилках для мебели и столярных изделий, способствуя эстетической привлекательности и защите деревянных поверхностей.
Применяется в покрытиях и отделках автомобильных компонентов, обеспечивая защитный слой без использования формальдегида, обеспечивая безопасность и соответствие экологическим нормам.

Используется в полиграфической промышленности для приготовления печатных красок и покрытий, способствуя безопасности работников и снижению воздействия на окружающую среду.
Используется в процессах очистки воды, где эти полимеры способствуют флокуляции и осаждению без введения формальдегида в водные системы.
Применяется в кожевенной промышленности для создания покрытий для кожгалантереи, обеспечивающих защиту и улучшающих внешний вид без использования формальдегида.

Orgal p 839 w используется в рецептуре герметиков для воздуховодов отопления, вентиляции и кондиционирования воздуха (HVAC), обеспечивая эффективную герметизацию без выделения формальдегида.
Некоторые акриловые полимеры, не содержащие формальдегида, являются биоразлагаемыми, что способствует созданию более устойчивых и экологически чистых составов.
Применяются в качестве связующих и матричных смол при производстве композиционных материалов, способствуя прочности и долговечности без содержания формальдегида.

Orgal p 839 w используется в качестве модификаторов реологии в различных составах для воздействия на вязкость и текучесть, улучшения эксплуатационных характеристик.
Содержится в прокладках и герметиках для автомобильного применения, обеспечивая эффективную герметизацию без использования формальдегида.
Orgal p 839 w используется в рецептуре клеев для упаковочных материалов, обеспечивая прочное сцепление без введения формальдегида в упаковку.

Акриловые полимеры, не содержащие формальдегида, обычно используются в производстве красок на водной основе, способствуя снижению выбросов летучих органических соединений и улучшению экологических показателей.
Используется в производстве клеев для электронной промышленности, обеспечивающих эффективное склеивание без включения формальдегида.
Orgal p 839 w используется в рецептуре покрытий для упаковочных материалов, таких как картон и бумага, обеспечивая защиту и пригодность для печати без включения формальдегида.

Акриловые полимеры, не содержащие формальдегида, могут использоваться в производстве медицинских клеев, обеспечивая безопасное и эффективное склеивание в медицинских целях.
Содержится в клеях, используемых для этикеток, наклеек и лент, обеспечивая прочную адгезию без использования формальдегида.
Включается в составы для контроля пенообразования в различных промышленных процессах, таких как краски, покрытия и клеи, без введения формальдегида.

Orgal p 839 w используется в производстве средств гигиены, таких как гигиенические прокладки и подгузники, где для склеивания требуются клеи без содержания формальдегида.
Содержится в добавках для составов бетонов для улучшения таких свойств, как удобоукладываемость и прочность без использования формальдегида.

Включается в покрытия и составы в качестве ингибиторов коррозии, способствуя защите поверхностей без выделения формальдегида.
Orgal p 839 w используется в качестве разделительных агентов для пресс-форм в производственных процессах для облегчения выпуска формованных изделий без необходимости формальдегида.

Синонимы:
Оргал 74 С
Orgal Duraflex 84 S
Оргал 086ВР
Оргал 6830
Оргал PST 5010
Orgal PST 100 E
Оргал ПСТ 100
Orgal PST 50 E
Orgal P 806 S
Оргал 056В
Orgal K 6459 E
Orgal K 6455 E
Оргал PR 9464
Orgal PR 845 A
Оргал PR 842 А
Оргал 888
Оргал 878
Оргал 850 РР
Оргал 850
Orgal P 838 W
Orgal P 8266
Orgal P 8240
Оргал 826
Оргал 808
Оргал 050Г
Оргал 036В
Оргал 6820
Оргал 671
ORGAL P 839 Вт
ORGAL P 839 W - это акриловый полимер, не содержащий APEO, предназначенный для создания высококачественных грунтовок для блокировки морилок для дерева, стен, потолков и металлических поверхностей.
ORGAL P 839 W может использоваться в составах, содержащих оксид цинка и совместим с различными наполнителями и пигментами.
ORGAL P 839 W проявляет отличные пятноотталкивающие свойства, адгезию к древесине, устойчивость к мгновенной ржавлению.

Номер CAS: 105-59-9
Номер EINECS: 203-312-7

Синонимы: Orgal P 74 S, Orgal Duraflex 84 S, Orgal P 086VR, Orgal P 6830, Orgal PST 5010, Orgal PST 100 E, Orgal PST 100, Orgal PST 50 E, Orgal P 806 S, Orgal P 056V, Orgal K 6459 E, Orgal K 6455 E, Orgal PR 9464, Orgal PR 845 A, ORGAL P 839 W, Orgal P 888, Orgal P 878, Orgal P 850RR, Orgal P 850, Orgal P 838 W, Orgal P 8266, Orgal P 8240, Orgal P 826, Orgal P 808, Orgal P 050G, Orgal P 036V, Orgal P 6820, Orgal P 671, Orgal P 653, Orgal P 600, Orgal P 062 V, Orgal P 526, Orgal P 523V, Orgal PST 50 A, Orgal PR 667, Orgal PR 670, Orgal PST 65, Orgal ORGAWHITE 2000, ORGAL M 340, ORGAL M 420 (Акрилик), ORGAL HT 465 (HAZ), Orgal P 086V, Orgal P 090V, Orgal seks 3011, Orgal CX 3015-X, Orgal CX 3060, N-МЕТИЛДИЭТАНОЛАМИН, 105-59-9, Бис(гидроксиэтил)метиламин, Метилдиэтаноламин, 2,2'-(Метилимино)дитанол, Метилдиэтаноламин, Этанол, 2,2'-(метилимино)бис-, 591248-66-7, N-метиламинодигликол, N-метилиминодитанол, N-метил-2,2'-иминодитанол, 2,2'-метилиминдиэтанол, N-метилдиэтанолимин, 2-[2-гидроксиэтил(метил)амино]этанол, ВВС США DO-52, N,N-бис(2-гидроксиэтил)метиламин, бис(2-гидроксиэтил)метиламин, метилбис(2-гидроксиэтил)амин, диэтанометиламин, метилиминдитанол, этанол, 2,2'-(метилимино)ди-, N-метилдиэтаноламин, N,N-ди(2-гидроксиэтил)-N-метиламин, бис(2-гидроксиэтил)метиламин, NSC 11690, 2-( N-2-гидроксиэтил-N-метиламино)этанол, 3IG3K131QJ, N-метилимин-2,2'-дитанол, DTXSID8025591, 2-[(2-гидроксиэтил)(метил)амино]этан-1-ол, NSC-11690, этанол,2'-(метилимино)ди-, этанол,2'-(метилимино)бис-, WLN: Q2N1 & 2Q, CCRIS 4843, N-метил-диэтаноламин, EINECS 203-312-7, BRN 1734441, UNII-3IG3K131QJ, бис-(гидроксиэтил)метиламин, HSDB 6804, Mdea (диол), N-метилдетаноламн, n-метилдиэтаноламин, метилдиэтаноламин, N-метил-дитаноламин диэтанол-амин, аминоспирт mda, ди(гидроксиэтил)метиламин, EC 203-312-7, 2-гидрокси-1-[(2-гидроксиэтил)метиламино]-этил, SCHEMBL17605.

ORGAL P 839 Безформальдегидный акриловый полимер, предназначенный для нанесения высокоэффективных покрытий в различных наружных и внутренних работах, древесных покрытий, морилок для дерева.
При использовании в покрытиях на водной основе он демонстрирует адгезию во влажной и сухой воде, отличную внешнюю прочность, стойкость к трещинам, мелу и щелочам, сохранение блеска и оттенка, а также отличную реакцию на модификатор реологии.
ORGAL P 839 W демонстрирует алкидную совместимость и прозрачность в морилках для дерева. Максимальный срок годности составляет 12 месяцев.

ORGAL P 839 W подходит для различных наружных и внутренних работ, включая покрытия для дерева и морилки для дерева.
При использовании в ORGAL P 839 W он демонстрирует отличную адгезию во влажной и сухой воде, исключительную долгове��ность снаружи и устойчивость к трещинам, мелу и щелочам.
ORGAL P 839 W также сохраняет блеск и оттенок и обладает отличной реологической реологической реакцией.

ORGAL P 839 W отличается тщательно продуманными механическими свойствами, повышающими стойкость к холодному контролю.
Акриловый полимер, не содержащий формальдегида, относится к акриловому полимеру, полученному без использования формальдегида или с минимальным содержанием формальдегида в его составе.
ORGAL P 839 W — это химическое соединение, традиционно используемое в производстве некоторых смол и полимеров, но оно также известно своей потенциальной опасностью для здоровья.

Акриловая основа ORGAL P 839 W обеспечивает превосходную долговечность снаружи.
ORGAL P 839 W демонстрирует алкидную совместимость и прозрачность в морилках для дерева. Максимальный срок хранения ORGAL P 839 W составляет 12 месяцев.
ORGAL P 839 W – отличный выбор для самодельных покрытий и красок для дерева на минеральных поверхностях.

ORGAL P 839 W позволяет достичь очень низких показателей водопроницаемости в соответствии со стандартом EN 927-5.
При высыхании при температуре выше 10°C ORGAL P 839 W образует прозрачную и глянцевую пленку средней твердости.
ORGAL P 839 W обладает превосходным связыванием пигмента, обеспечивая очень высокую стойкость к истиранию даже при высоких уровнях ПВХ (объемной концентрации пигмента).

ORGAL P 839 W представляет собой винилацетатно-акриловый сополимер, что означает, что он содержит в своей молекулярной структуре как винилацетат, так и акриловые мономерные единицы.
ORGAL P 839 W универсален и прост в составлении, обладает очень хорошей стойкостью к истиранию и долговечностью на открытом воздухе.
ORGAL P 839 W используется для широкого спектра применений, включая большинство внутренних покрытий от плоских до полуглянцевых, текстурированных покрытий, грунтовок и штукатурок. ORGAL P 839 W - это сополимер стирола и акрила, специально разработанный для использования в матовых и полуглянцевых красках для стен без растворителей для внутренних и наружных работ со слабым запахом.

ORGAL P 839 W не содержит летучих органических соединений (ЛОС), этоксилатов алкилфенола, аммиака и формальдегида.
ORGAL P 839 W устойчив к жидкому стеклу и может использоваться в составах силикатных красок.
ORGAL P 839 W обеспечивает отличное пленкообразование без использования коалесцирующих агентов.

Краски на основе ORGAL P 839 W демонстрируют отличную стойкость к мокрым царапинам, щелочам и грязевым трещинам при высоких диапазонах ПВХ, а также высокую способность связывания пигментов.
ORGAL P 839 W обычно используется в рецептурах клеев, обеспечивая необходимые для адгезии адгезионные свойства без использования формальдегида.
В лакокрасочной промышленности ORGAL P 839 W используется для создания пленок, которые хорошо прилипают к поверхностям, обеспечивают долговечность и демонстрируют низкий уровень выбросов летучих органических соединений.

ORGAL P 839 W также может использоваться в текстильной промышленности, в частности, в производстве покрытий для тканей, обладающих такими свойствами, как водоотталкивающие свойства и устойчивость к пятнам.
Кроме того, ORGAL P 839 W может использоваться в составлении герметиков для систем отопления, вентиляции и кондиционирования воздуха (ОВКВ), способствуя общей эффективности и безопасности систем ОВКВ.
ORGAL P 839 W — это разновидность полимера на основе акриловой эмульсии.

Акриловые эмульсии ORGAL P 839 W используются в различных областях, включая краски, покрытия, клеи и текстиль.
Эти полимеры известны своей отличной адгезией, гибкостью, водостойкостью и долговечностью.
ORGAL P 839 W подходит для грунтовок для внутренних поверхностей, блокирующих танин/пятна, грунтовок для древесины, грунтовочных грунтовок и грунтовок с устойчивостью к вспышкам и ранней ржавчине на металлических поверхностях.

Максимальный срок хранения ORGAL P 839 W составляет 12 месяцев.
Конкретные свойства и применение ORGAL P 839 W зависят от его рецептуры и предполагаемого использования, которое может быть предоставлено производителем или поставщиком продукта.
ORGAL P 839 W — линейка полимерных эмульсий на основе акриловой, стирол-акриловой и винилакриловой химии.

Эти продукты соответствуют нормам ЛОС, постепенно отказываясь от формальдегида, аммиака и других запрещенных веществ.
ORGAL P 839 W — линейка полимерных эмульсий на основе акриловой, стирол-акриловой и винилакриловой химии.
Эти продукты соответствуют нормам ЛОС, постепенно отказываясь от формальдегида, аммиака и других запрещенных веществ.

ORGAL P 839 W, также известный как N-метилдиэтаноламин и чаще как MDEA, представляет собой органическое соединение с формулой CH3N(C2H4OH)2.
ORGAL P 839 W представляет собой бесцветную жидкость с запахом аммиака.
ORGAL P 839 W смешивается с водой, этанолом и бензолом.

Третичный амин, он широко используется в качестве подсластителя в химической, нефтеперерабатывающей, синтез-газовой промышленности и природном газе.
Аналогичными соединениями являются ORGAL P 839 W, первичный амин, и диэтаноламин (DEA), вторичный амин, оба из которых также используются для обработки аминового газа.

Химический состав: AC
MFFT (°C): 9± 1
Tg (°C): 12
Полимерная структура: AC

ORGAL P 839 W используется в производстве клеев для ковровых покрытий и напольных покрытий.
Это применение помогает гарантировать, что в помещениях, где обычно используются эти материалы, снижен уровень выбросов формальдегида.
ORGAL P 839 W находит применение в рецептурах древесных покрытий и отделок для мебели и шкафов. Эти покрытия обеспечивают защиту, улучшают эстетику и способствуют повышению безопасности в помещении.

ORGAL P 839 W можно использовать в покрытиях для бумажных и картонных изделий, обеспечивая улучшенные печатные свойства, влагостойкость и общую долговечность.
ORGAL P 839 W используется в рецептурах герметиков для строительных работ.
Эти герметики обеспечивают адгезионные свойства и гибкость, избегая при этом потенциальных проблем со здоровьем, связанных с выделением формальдегида.

В кожевенной промышленности ORGAL P 839 W может применяться в производстве покрытий для кожаных изделий, обеспечивающих защитные и эстетические свойства без использования формальдегида.
ORGAL P 839 W может функционировать в качестве модификаторов реологии в различных составах.
Эти модификаторы влияют на вязкость и текучесть материала, способствуя его применению и эксплуатационным характеристикам.

В соответствии с устойчивыми и экологически чистыми методами, некоторые составы ORGAL P 839 W разработаны как биоразлагаемые, что позволяет решить проблемы воздействия некоторых химических веществ на окружающую среду.
ORGAL P 839 W обычно используется в производстве полимерных эмульсий.
Эти эмульсии находят применение в самых разных отраслях промышленности, включая краски, покрытия и клеи.

ORGAL P 839 W также используется в рецептурах герметиков и составов для швов в строительстве и благоустройстве дома.
ORGAL P 839 W подходит для герметизации и отделки без добавления формальдегида.
ORGAL P 839 W используется в покрытиях для бетонных полов и стен, обеспечивая долговечность и устойчивость к истиранию и химическим веществам.

ORGAL P 839 W используется в производстве PSA для лент, этикеток и наклеек благодаря своим сильным адгезионным свойствам к липкости и отслаиванию.
ORGAL P 839 W используется в рецептурах клеев для строительных материалов, обеспечивая прочное сцепление с такими основаниями, как дерево, металл и пластик.
Наносится на ткани для придания водонепроницаемости, огнестойкости и повышенной долговечности, не влияя на текстуру и гибкость ткани.

ORGAL P 839 W используется в качестве связующего вещества в нетканых материалах для гигиенических изделий, фильтрующих материалов и геотекстиля, обеспечивая прочность и структурную целостность.
Входит в состав герметиков, используемых для герметизации швов и щелей в зданиях, обеспечивая гибкость, устойчивость к атмосферным воздействиям и адгезию к различным основаниям.
ORGAL P 839 W используется в автомобильной промышленности для герметизации швов и соединений, обеспечивая долговечность и устойчивость к воздействию тепла и автомобильных жидкостей.

ORGAL P 839 W часто подвергается исследованиям и разработкам, направленным на улучшение его эксплуатационных характеристик или расширение области применения.
Включение наночастиц для улучшения таких свойств, как устойчивость к царапинам, термическая стабильность и антимикробная активность.
Разработка био или экологически чистых вариантов для снижения воздействия на окружающую среду и повышения устойчивости.

Интеграция в «умные» покрытия, которые могут реагировать на раздражители окружающей среды, такие как температура, pH или механическое воздействие, обеспечивая такие функции, как самовосстановление или изменение цвета.
Производители и поставщики ORGAL P 839 W обычно предлагают всестороннюю техническую поддержку, чтобы помочь клиентам оптимизировать рецептуры и процессы нанесения.
Помощь в разработке рецептур, отвечающих конкретным требованиям к производительности.

Доступ к услугам по тестированию для оценки эффективности разработанных продуктов в различных условиях.
Предоставление учебных занятий и учебных материалов для обеспечения правильного обращения, применения и техники безопасности.
ORGAL P 839 W - это акриловый полимер, не содержащий APEO, предназначенный для создания высококачественных грунтовок для блокировки морилок для дерева, стен, потолков и металлических поверхностей.

ORGAL P 839 W может использоваться в составах, содержащих оксид цинка и совместим с различными наполнителями и пигментами.
ORGAL P 839 W проявляет отличные пятноотталкивающие свойства, адгезию к древесине, устойчивость к мгновенной ржавлению.
ORGAL P 839 W подходит для грунтовок для внутренних поверхностей, блокирующих танин/пятна, грунтовок для древесины, грунтовочных грунтовок и грунтовок с устойчивостью к вспышкам и ранней ржавчине на металлических поверхностях.

Максимальный срок хранения ORGAL P 839 W составляет 12 месяцев.
ORGAL P 839 W менее реакционноспособен по отношению к CO2, но имеет равновесную нагрузочную способность, приближающуюся к 1 моль CO2 на моль амина.

Использует:
ORGAL P 839 W используется в рецептурах клеев для различных областей применения, включая деревообработку, строительство и упаковку.
Эти клеи обеспечивают связующие свойства без использования формальдегида.
ORGAL P 839 W используется в производстве покрытий и красок для таких поверхностей, как стены, мебель и автомобильные компоненты.

Эти покрытия способствуют долговечной отделке с меньшим воздействием на окружающую среду.
Используемый в строительных герметиках и герметиках, ORGAL P 839 W обеспечивает эффективную герметизацию без необходимости использования формальдегида.
Эти полимеры обычно используются в таких областях, как установка окон, швов и зазоров.

ORGAL P 839 W используется в текстильной промышленности для создания отделки тканей, обеспечивая такие свойства, как водоотталкивающие свойства, устойчивость к сминанию и огнестойкость без добавления формальдегида.
При нанесении покрытий на бумагу и картон ORGAL P 839 W улучшает такие свойства, как пригодность для печати, влагостойкость и общая долговечность, не способствуя выделению формальдегида.
ORGAL P 839 W - это специальный полимер на основе акриловой эмульсии, предназначенный для использования в различных покрытиях и клеях.

ORGAL P 839 W обычно используется в составах, требующих баланса между производительностью и соблюдением экологических норм.
ORGAL P 839 W можно использовать в сочетании с другими полимерами и добавками для достижения желаемых свойств в конечном продукте.
ORGAL P 839 W используется в рецептурах красок для внутренних стен, которые требуют хорошей моющейся способности, устойчивости к пятнам и эстетической привлекательности.

Идеально подходит для наружных покрытий благодаря своей устойчивости к ультрафиолетовому излучению и долговечности, защищая поверхности от суровых погодных условий.
Обеспечивает отличную адгезию и коррозионную стойкость для металлических поверхностей, подходит для промышленного оборудования и конструкций.
Используется в покрытиях для бетонных полов и стен, обеспечивая долговечность и устойчивость к истиранию и химическим веществам.

ORGAL P 839 W используется в производстве лент, этикеток и наклеек благодаря своим сильным адгезионным свойствам к липкости и отслаиванию.
Разработан для прочного сцепления с такими строительными материалами, как дерево, металл и пластик.
Применяется в упаковке для склеивания различных материалов, таких как бумага, картон и пластик.

Наносится на ткани для обеспечения водонепроницаемости, огнестойкости и повышенной прочности без ущерба для текстуры и гибкости.
ORGAL P 839 Wis используется в качестве связующего вещества в нетканых материалах для гигиенических изделий, фильтрующих материалах и геотекстиле, обеспечивая прочность и структурную целостность.
Входит в состав герметиков для герметизации швов и щелей в зданиях, обеспечивая гибкость, устойчивость к атмосферным воздействиям и адгезию к различным основаниям.

ORGAL P 839 W используется в автомобильной промышленности для герметизации швов и соединений, обеспечивая долговечность и устойчивость к воздействию тепла и автомобильных жидкостей.
ORGAL P 839 W используется в защитных покрытиях для различных поверхностей, обеспечивая устойчивость к факторам окружающей среды, таким как влага, химические вещества и истирание.
Разработан для декоративных целей, обеспечивая эстетическую отделку с долговечностью и защитой.

Применяется в покрытиях из бумаги и картона для улучшения таких свойств, как блеск, гладкость и пригодность для печати.
ORGAL P 839 W используется в упаковочных пленках для придания барьерных свойств и улучшения внешнего вида упакованных товаров.
ORGAL P 839 W используется в качестве модификатора в составах цемента и бетона для улучшения таких свойств, как адгезия, гибкость и долговечность.

В состав входят клеи для плитки, обеспечивающие прочное сцепление и устойчивость к влаге и перепадам температуры.
ORGAL P 839 W используется в покрытиях для деревянной мебели для улучшения внешнего вида, защиты от износа, а также обеспечения устойчивости к факторам окружающей среды.
Применяется в покрытиях для деревянных полов для долговечности, устойчивости к царапинам и простоте ухода.

ORGAL P 839 W используется в автомобильных красках и покрытиях благодаря своей превосходной адгезии, долговечности и устойчивости к факторам окружающей среды.
Входит в состав покрытий для внутренних автомобильных компонентов для обеспечения долговечной и эстетически привлекательной отделки.
ORGAL P 839 W используется в покрытиях для лодок и морских сооружений, обеспечивая защиту от воды, соли и других суровых морских условий.

Применяется в покрытиях для промышленного оборудования для защиты от износа, коррозии и химического воздействия.
ORGAL P 839 W используется в покрытиях для различного промышленного оборудования, обеспечивая долговечность и устойчивость к суровым условиям эксплуатации.
Разработан в продуктах «сделай сам» для ремонта и благоустройства дома, обеспечивает простоту нанесения и надежную работу.

ORGAL P 839 W используется в декоративной отделке для домашних интерьеров и экстерьеров, обеспечивая как защиту, так и эстетическое улучшение.
Идеально подходит для использования в красках для потолков благодаря своей способности обеспечивать гладкое, матовое покрытие с отличным покрытием.
ORGAL P 839 W используется в качестве базового покрытия для подготовки поверхностей к покраске, обеспечивая лучшую адгезию и равномерную отделку.

Обеспечивает длительную защиту машин и оборудования, работающих в суровых промышленных условиях.
Обеспечивает защитный барьер для предотвращения ржавчины и коррозии на металлических поверхностях.
ORGAL P 839 W используется в покрытиях днища автомобилей для защиты от коррозии, дорожных солей и механических повреждений.

Обеспечивает хорошую адгезию и долговечность на пластиковых деталях, используемых в автомобильных интерьерах и экстерьерах.
Применяется на корпусах лодок и кораблей для защиты от повреждений водой, обрастания и морской растительности.
ORGAL P 839 W используется в полиграфической промышленности для разработки рецептур печатных красок и покрытий, способствуя повышению безопасности работников и снижению воздействия на окружающую среду.

ORGAL P 839 W используется в процессах очистки воды, где эти полимеры способствуют флокуляции и осаждению без введения формальдегида в водные системы.
Применяемый в кожевенной промышленности, ORGAL P 839 W создает покрытия для кожаных изделий, обеспечивая защиту и улучшая внешний вид без использования формальдегида.
ORGAL P 839 W используется в рецептуре герметиков для систем отопления, вентиляции и кондиционирования воздуха (ОВКВ), обеспечивая эффективную герметизацию без выделения формальдегида.

Некоторые акриловые полимеры, не содержащие формальдегида, в том числе ORGAL P 839 W, являются биоразлагаемыми, что способствует созданию более устойчивых и экологически чистых составов.
Он применяется в качестве связующих и матричных смол при производстве композитных материалов, повышая прочность и долговечность без содержания формальдегида.
ORGAL P 839 W служит в качестве модификаторов реологии в различных составах, влияя на вязкость и свойства текучести для улучшения эксплуатационных характеристик.

ORGAL P 839 W содержится в прокладках и герметиках для автомобильной промышленности, обеспечивая эффективную герметизацию без использования формальдегида.
ORGAL P 839 W используется в рецептуре клеев для упаковочных материалов, обеспечивая прочное сцепление без внесения формальдегида в упаковку.
Акриловые полимеры, не содержащие формальдегида, обычно используются в производстве красок на водной основе, способствуя снижению выбросов летучих органических соединений и улучшению экологических характеристик.

Они содержатся в клеях, используемых в электронной промышленности, обеспечивая эффективное склеивание без включения формальдегида.
ORGAL P 839 W используется в рецептуре покрытий для упаковочных материалов, таких как картон и бумага, обеспечивая защиту и пригодность для печати без включения формальдегида.
Акриловые полимеры, не содержащие формальдегида, могут использоваться в производстве медицинских клеев, обеспечивая безопасное и эффективное склеивание в медицинских целях.

Они содержатся в клеях, используемых для этикеток, наклеек и лент, обеспечивая прочную адгезию без использования формальдегида.
Входит в составы для контроля пенообразования в различных промышленных процессах, таких как краски, покрытия и клеи, без введения формальдегида.
ORGAL P 839 W используется в производстве средств гигиены, таких как гигиенические прокладки и подгузники, где для склеивания требуются клеи без содержания формальдегида.

ORGAL P 839 W содержится в добавках для составов бетонов для улучшения таких свойств, как удобоукладываемость и прочность, без использования формальдегида.
Входит в состав покрытий и составов в качестве ингибиторов коррозии, способствуя защите поверхностей без выделения формальдегида.
ORGAL P 839 W используется в качестве разделительных составов для пресс-форм в производственных процессах для облегчения выпуска формованных изделий без необходимости использования формальдегида.

Профиль безопасности:
ORGAL P 839 W используется в хорошо проветриваемых помещениях или с соответствующими средствами защиты органов дыхания.
Не ешьте, не пейте и не курите при использовании этого продукта.
Тщательно вымойте руки после работы.

Несмотря на то, что в целом в нем мало летучих органических соединений, неправильная утилизация может оказать воздействие на окружающую среду.
Избегайте попадания в окружающую среду.
Утилизируйте содержимое/контейнер в соответствии с местными правилами.

Вымойте большим количеством воды с мылом.
При появлении раздражения кожи или сыпи обратитесь за медицинской помощью.
Осторожно смойте водой в течение нескольких минут.

Снимите контактные линзы, если они есть и это легко сделать.
Если раздражение глаз не проходит, обратитесь за медицинской помощью.
Выведите человека на свежий воздух и держите его удобным для дыхания.

Если дыхание затруднено, немедленно обратитесь за медицинской помощью.
Длительный или повторный контакт с кожей может вызвать раздражение или дерматит.
Надевайте защитные перчатки и избегайте прямого контакта с кожей.

Может вызвать раздражение глаз при контакте.
ORGAL P 839 W - это защитные очки или лицевой щиток для защиты глаз.
Вдыхание аэрозоля или тумана может вызвать раздражение дыхательных путей.



ORGAL P 850 RR
Orgal P 850 RR демонстрирует превосходную стойкость к истиранию и ультрафиолетовому излучению.
Orgal P 850 RR подходит для большинства матовых и глянцевых покрытий для внутренних и наружных работ, включая акриловую яичную скорлупу для кухонь и ванных комнат.


Тип продукта: Акрилы и акриловые сополимеры > Акриловые эмульсии
Химический состав: Акриловый полимер.
Физическая форма: Эмульсия


Orgal P 850 RR — это акриловый полимер, не содержащий APEO и формальдегида, обладающий превосходной стойкостью к внешним воздействиям, потенциалом глянца, прозрачностью банки и реакцией на загуститель.
Orgal P 850 RR демонстрирует превосходную стойкость к истиранию и ультрафиолетовому излучению.


Orgal P 850 RR демонстрирует хорошую адгезию во влажных и сухих условиях.
Высушенные пленки на основе Orgal P 850 RR демонстрируют хорошую стойкость к слипанию, пожелтению и водостойкость.
Orgal P 850 RR подходит для большинства матовых и глянцевых покрытий для внутренних и наружных работ, включая акриловую яичную скорлупу для кухонь и ванных комнат.


Orgal P 850 RR также подходит для пропиток для дерева, красок для бетонных полов и грунтовок.
Максимальный срок хранения Оргал П 850 РР составляет 12 месяцев.



ИСПОЛЬЗОВАНИЕ И ПРИМЕНЕНИЕ ORGAL P 850 RR:
Области применения Orgal P 850 RR: Краски и морилки для дерева своими руками.
Orgal P 850 RR демонстрирует превосходную стойкость к истиранию и ультрафиолетовому излучению.
Orgal P 850 RR демонстрирует хорошую адгезию во влажных и сухих условиях.


Высушенные пленки на основе Orgal P 850 RR демонстрируют хорошую стойкость к слипанию, пожелтению и водостойкости.
Orgal P 850 RR подходит для большинства матовых и глянцевых покрытий для внутренних и наружных работ, включая акриловую яичную скорлупу для кухонь и ванных комнат.
Orgal P 850 RR также подходит для пропиток для дерева, красок для бетонных полов и грунтовок.



ХАРАКТЕРИСТИКИ ORGAL P 850 RR:
*Внешние краски
*Отличный



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ORGAL P 850 RR:
Название продукта: ORGAL P 850 RR
Химический состав: Акриловый полимер.
Всего твердых веществ (% ±1): 50
рН: 8,0
Вязкость (мПа.с макс.): 1000
MFFT (°C): 18
Тс (°С): 22
Внешний вид: Белая эмульсия
Структура полимера: переменный ток
Тип продукта: Акрилы и акриловые сополимеры > Акриловые эмульсии
Физическая форма: Эмульсия

Общая информация:
Химический состав: переменный ток
Всего твердых веществ (% ±1): 50
pH: 8,0–9,0
Вязкость по Брукфилду (мПас): 200–1000
MFFT (°C): 18 ± 1
Тс (°С): 22 ± 1
Внешний вид: Белая эмульсия
Структура полимера: переменный ток
Тип продукта: Акрилы и акриловые сополимеры > Акриловые эмульсии
Физическая форма: Эмульсия



МЕРЫ ПЕРВОЙ ПОМОЩИ ORGAL P 850 RR:
-Описание мер первой помощи.
*Общие советы:
Покажите этот паспорт безопасности материала лечащему врачу.
*При вдыхании:
После ингаляции:
Свежий воздух.
*При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промыть кожу с
вода/душ.
*В случае зрительного контакта:
После зрительного контакта:
Промойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.
*При проглатывании:
После глотания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.
-Указание на необходимость немедленной медицинской помощи и специального лечения.
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ ORGAL P 850 RR:
-Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Закройте дренажи.
Соберите, свяжите и откачайте пролитую жидкость.
Соблюдайте возможные ограничения по материалам.
Возьмите в сухом виде.
Утилизируйте должным образом.
Очистите пораженный участок.



МЕРЫ ПОЖАРОТУШЕНИЯ ORGAL P 850 RR:
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Углекислый газ (CO2)
Мыло
Сухой порошок
*Неподходящие средства пожаротушения:
Для этого вещества/смеси не установлены ограничения по огнетушащим веществам.
-Дальнейшая информация:
Не допускайте попадания воды для пожаротушения в поверхностные воды или систему грунтовых вод.



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/ПЕРСОНАЛЬНАЯ ЗАЩИТА ORGAL P 850 RR:
-Параметры управления:
--Ингредиенты с параметрами контроля на рабочем месте:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
*Защита глаз/лица:
Используйте средства защиты глаз.
Безопасные очки
*Защита тела:
защитная одежда
*Защита органов дыхания:
Рекомендуемый тип фильтра: Фильтр A
-Контроль воздействия на окружающую среду:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ORGAL P 850 RR:
-Условия безопасного хранения, включая любые несовместимости:
*Условия хранения:
Плотно закрыто.
Сухой.



СТАБИЛЬНОСТЬ И РЕАКЦИОННАЯ СПОСОБНОСТЬ ORGAL P 850 RR:
-Химическая стабильность:
Продукт химически стабилен при стандартных условиях окружающей среды (комнатная температура).
-Возможность опасных реакций:
Данные недоступны


ORGAL P 878
Orgal P 878 представляет собой акриловый полимер, разработанный для высокоэффективных покрытий для различных наружных и внутренних работ.


Тип продукта: акрилы и акриловые сополимеры
Химический состав: Акриловый полимер


Orgal P 878 не свободен от APEO и демонстрирует адгезию во влажном и сухом состоянии, отличную внешнюю стойкость, устойчивость к быстрому смыванию, стойкость к воде, истиранию, царапинам, трещинам, мелу и щелочам в покрытиях на водной основе.
Orgal P 878 также обеспечивает сохранение блеска и оттенка и превосходную реакцию на модификаторы реологических свойств.
Orgal P 878 имеет максимальный срок годности 12 месяцев.



ПРИМЕНЕНИЕ ORGAL P 878:
Orgal P 878 используется для латекса для обработки красок.
Благодаря своей гидрофобной и прочной природе, краски и прозрачные покрытия на основе Orgal P 878 обладают отличной водостойкостью и адгезией к пористым основаниям, стойкостью к быстрому смыванию (дождю), а также очень хорошей стойкостью к слипанию, истиранию и поглощению грязи. .



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ORGAL P 878:
Тип продукта: акрилы и акриловые сополимеры
Химический состав: Акриловый полимер
Физическая форма: Эмульсия



МЕРЫ ПЕРВОЙ ПОМОЩИ ORGAL P 878:
-Описание мер первой помощи:
*Общие рекомендации:
Покажите этот паспорт безопасности материала лечащему врачу.
*При вдыхании:
После вдоха:
Свежий воздух.
Вызовите врача.
*При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промойте кожу водой/душем.
Проконсультируйтесь с врачом.
*При попадании в глаза:
После зрительного контакта:
Смойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.
* При проглатывании:
После проглатывания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.
- Указание на необходимость немедленной медицинской помощи и специального лечения:
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ ORGAL P 878:
- Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Закрыть стоки.
Собирайте, связывайте и откачивайте разливы.
Соблюдайте возможные ограничения по материалам.
Бери насухо.
Утилизируйте правильно.
Очистите пораженный участок.



ПРОТИВОПОЖАРНЫЕ МЕРЫ ORGAL P 878:
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Используйте меры пожаротушения, соответствующие местным условиям и
окружающая среда.
*Неподходящие средства пожаротушения:
Для этого вещества/смеси не даются ограничения огнетушащих веществ.
-Дальнейшая информация:
Предотвратить загрязнение поверхностных вод или системы грунтовых вод водой для пожаротушения.



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/СРЕДСТВА ИНДИВИДУАЛЬНОЙ ЗАЩИТЫ ORGAL P 878:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
* Защита глаз/лица:
Используйте средства защиты глаз.
Безопасные очки
* Защита кожи:
Полный контакт:
Материал: Нитриловый каучук
Минимальная толщина слоя: 0,11 мм
Время прорыва: 480 мин.
Всплеск контакта:
Материал: Нитриловый каучук
Минимальная толщина слоя: 0,11 мм
Время прорыва: 480 мин.
* Защита тела:
защитная одежда
-Контроль воздействия окружающей среды:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ORGAL P 878:
- Меры предосторожности для безопасного обращения:
*Советы по безопасному обращению:
Работа под капотом.
*Гигиенические меры:
Немедленно смените загрязненную одежду.
Применяйте профилактическую защиту кожи.
Вымойте руки и лицо после работы с веществом.
-Условия для безопасного хранения, включая любые несовместимости:
*Условия хранения:
Плотно закрытый.
Сухой.
Хранить под замком или в месте, доступном только для квалифицированных или уполномоченных лиц.



СТАБИЛЬНОСТЬ и РЕАКЦИОННАЯ СПОСОБНОСТЬ ORGAL P 878:
-Реактивность:
Данные недоступны
-Химическая стабильность:
Продукт химически стабилен в стандартных условиях окружающей среды (комнатная температура).
-Условия, чтобы избежать:
Нет доступной информации
-Несовместимые материалы:
Данные недоступны



ORGAL PR 667
Orgal pr 667 представляет собой стирольно-акриловый сополимер низкой вязкости с очень мелкими частицами.
Orgal pr 667 обеспечивает слегка липкую, эластичную и прозрачную пленку.
Orgal pr 667 обеспечивает слегка липкую, эластичную и прозрачную пленку.


Orgal pr 667 обладает превосходными проникающими свойствами, долговечностью и адгезией.
Orgal pr 667 подходит для производства водных грунтовок высокой проникающей способности и морилок для древесины.
Оргал пр 667 обеспечивает высокую устойчивость к щелочным средам.


Оргал пр 667 совместим с гипсом и гипсокартонами.
Максимальный срок хранения – 12 месяцев.
Оргал пр 667 представляет собой эмульсию стирола-акрилового сополимера с очень мелким размером частиц.


Orgal pr 667 предназначен как для грунтовок, так и может включаться в составы морилок.
Оргал пр 667 – выпускается в виде маловязкой эмульсии от голубоватого до белого оттенка.
Оргал пр 667 позволяет получить пленку слегка липкую, эластичную и прозрачную.


Благодаря очень маленькому размеру частиц Orgal pr 667 обладает отличными проникающими и адгезионными свойствами.
Для обеспечения надежного хранения Оргала пр 667 тару необходимо очень хорошо укупоривать, чтобы не допустить испарения воды и образования оболочки.
Оргал pr 667 следует хранить при температуре 5–25°C не более 12 месяцев, не допуская замораживания.



ИСПОЛЬЗОВАНИЕ И ПРИМЕНЕНИЕ ORGAL PR 667:
Использование Orgal pr 667 для морилки: Отлично.
Orgal pr 667 предназначен как для грунтовок, так и может включаться в составы морилок.
Оргал пр 667 – выпускается в виде маловязкой эмульсии от голубоватого до белого оттенка.
Оргал пр 667 позволяет получить пленку слегка липкую, эластичную и прозрачную.
Благодаря очень маленькому размеру частиц Orgal pr 667 обладает отличными проникающими и адгезионными свойствами.



ОБЛАСТЬ ПРИМЕНЕНИЯ ОРГАЛА ПР 667:
Orgal pr 667, благодаря очень маленькому размеру частиц, особенно хорошо работает с сильно проникающими грунтами на водной основе, шпаклевками, цементами и асбестоцементами.
При этом проникающая способность увеличивается при уменьшении количества сухого остатка и добавлении небольших количеств ПАВ.
Пропорции разведения определяются экспериментальным путем.

Полученные покрытия обладают хорошей стойкостью к щелочным средам, совместимы с гипсом и изделиями из Оргала пр 667.
- Отличная проникающая способность
- Отличная адгезия
- Отличная износостойкость



ХАРАКТЕРИСТИЧЕСКИЕ СВОЙСТВА ОРГАЛА ПР 667:
Внешний вид Молочно-белая жидкость
Сухой остаток % ±1 34
Вязкость по Брукфилду RVT 1/20 макс. 100 спс.
pH 8,0–8,5
Мин. температура образования пленки 0°C
Температура стеклования 1°C



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ОРГАЛА ПР 667:
Химический состав: S/AC
Всего твердых веществ (%±1): 34
рН: 8,0-8,0
Вязкость (мПа.с макс): 100
MFFT (°C): 0
Тс (°С): 1



МЕРЫ ПЕРВОЙ ПОМОЩИ ОРГАЛА ПР 667:
-Описание мер первой помощи:
*Общие советы:
Покажите этот паспорт безопасности материала лечащему врачу.
*При вдыхании:
После ингаляции:
Свежий воздух.
*При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промойте кожу водой/душем.
*В случае зрительного контакта:
После зрительного контакта:
Промойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.
*При проглатывании:
После глотания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.
-Указание на необходимость немедленной медицинской помощи и специального лечения:
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ ORGAL PR 667:
-Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Закройте дренажи.
Соберите, свяжите и откачайте пролитую жидкость.
Соблюдайте возможные ограничения по материалам.
Возьмите в сухом виде.
Утилизируйте должным образом.
Очистите пораженное место.



МЕРЫ ПОЖАРОТУШЕНИЯ ОРГАЛА ПР 667:
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Вода
Мыло
Углекислый газ (CO2)
Сухой порошок
*Неподходящие средства пожаротушения:
Для этого вещества/смеси не установлены ограничения по огнетушащим веществам.
-Дальнейшая информация:
Не допускайте попадания воды для пожаротушения в поверхностные воды или систему грунтовых вод.



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/ПЕРСОНАЛЬНАЯ ЗАЩИТА ORGAL PR 667:
-Параметры управления:
--Ингредиенты с параметрами контроля на рабочем месте:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
*Защита глаз/лица:
Используйте средства защиты глаз.
Безопасные очки
*Защита кожи:
Полный контакт:
Материал: Нитриловый каучук.
Минимальная толщина слоя: 0,11 мм.
Время прорыва: 480 мин.
Всплеск контакта:
Материал: Нитриловый каучук.
Минимальная толщина слоя: 0,11 мм.
Время прорыва: 480 мин.
*Защита тела:
защитная одежда
*Защита органов дыхания:
Рекомендуемый тип фильтра: Тип фильтра P2.
-Контроль воздействия на окружающую среду:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ORGAL PR 667:
-Условия безопасного хранения, включая любые несовместимости:
*Условия хранения:
Плотно закрыто.
Сухой.



СТАБИЛЬНОСТЬ И РЕАКЦИОННАЯ СПОСОБНОСТЬ ORGAL PR 667:
-Химическая стабильность:
Продукт химически стабилен при стандартных условиях окружающей среды (комнатная температура).
-Несовместимые материалы:
Данные недоступны



ORGAL PR 845 A
Orgal PR 845 A обладает устойчивостью к ржавлению и отличной адгезией к древесине.


Тип продукта: Акрилы и акриловые сополимеры > Акриловые эмульсии
Химический состав: Акриловый сополимер.


Orgal PR 845 A — акриловый полимер, не содержащий APEO и оксидов цинка.
Orgal PR 845 A предназначен для высококачественных внутренних грунтовок, блокирующих танины и пятна, для дерева, грунтовок, стен, потолков и металлических поверхностей.
Orgal PR 845 A обладает устойчивостью к ржавлению и отличной адгезией к древесине.


Orgal PR 845 A позволяет создавать продукты с низким содержанием летучих органических соединений в соответствии с Директивой ЕС 2004/42/CE, поскольку он демонстрирует хорошие характеристики коалесценции при низких температурах.
Orgal PR 845 A совместим с оксидом цинка и различными наполнителями и пигментами.
Максимальный срок хранения Оргал PR 845 А составляет 12 месяцев.



ИСПОЛЬЗОВАНИЕ И ПРИМЕНЕНИЕ ORGAL PR 845 A:
Области применения Orgal PR 845 A: Краски для дома и защита от пятен.
Orgal PR 845 A предназначен для высококачественных внутренних грунтовок, блокирующих танины и пятна, для дерева, грунтовок, стен, потолков и металлических поверхностей.


Orgal PR 845 A обладает устойчивостью к ржавлению и отличной адгезией к древесине.
Orgal PR 845 A позволяет создавать продукты с низким содержанием летучих органических соединений в соответствии с Директивой ЕС 2004/42/CE, поскольку он демонстрирует хорошие характеристики коалесценции при низких температурах.
Orgal PR 845 A совместим с оксидом цинка и различными наполнителями и пигментами.



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ОРГАЛА ПР 845 А:
Название продукта: ОРГАЛ ПР 845 А
Химический состав: переменный ток
Всего твердых веществ (% ± 1): 46,5
рН: 8,0-8,0
Вязкость (мПа.с макс): 400
MFFT (°C): 3
Тс (°С): -1
Тип продукта: Акрилы и акриловые сополимеры > Акриловые эмульсии
Химический состав: Акриловый сополимер.
Физическая форма: эмульсия, опал.



МЕРЫ ПЕРВОЙ ПОМОЩИ ORGAL PR 845 A:
-Описание мер первой помощи.
*Общие советы:
Покажите этот паспорт безопасности материала лечащему врачу.
*При вдыхании:
После ингаляции:
Свежий воздух.
*При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промыть кожу с
вода/душ.
*В случае зрительного контакта:
После зрительного контакта:
Промойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.
*При проглатывании:
После глотания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.
-Указание на необходимость немедленной медицинской помощи и специального лечения.
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ ORGAL PR 845 A:
-Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Закройте дренажи.
Соберите, свяжите и откачайте пролитую жидкость.
Соблюдайте возможные ограничения по материалам.
Возьмите в сухом виде.
Утилизируйте должным образом.
Очистите пораженный участок.



МЕРЫ ПОЖАРОТУШЕНИЯ ORGAL PR 845 A:
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Углекислый газ (CO2)
Мыло
Сухой порошок
*Неподходящие средства пожаротушения:
Для этого вещества/смеси не установлены ограничения по огнетушащим веществам.
-Дальнейшая информация:
Не допускайте попадания воды для пожаротушения в поверхностные воды или систему грунтовых вод.



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/ПЕРСОНАЛЬНАЯ ЗАЩИТА ORGAL PR 845 A:
-Параметры управления:
--Ингредиенты с параметрами контроля на рабочем месте:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
*Защита глаз/лица:
Используйте средства защиты глаз.
Безопасные очки
*Защита тела:
защитная одежда
*Защита органов дыхания:
Рекомендуемый тип фильтра: Фильтр A
-Контроль воздействия на окружающую среду:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ORGAL PR 845 A:
-Условия безопасного хранения, включая любые несовместимости:
*Условия хранения:
Плотно закрыто.
Сухой.



СТАБИЛЬНОСТЬ И РЕАКЦИОННАЯ СПОСОБНОСТЬ ORGAL PR 845 A:
-Химическая стабильность:
Продукт химически стабилен при стандартных условиях окружающей среды (комнатная температура).
-Возможность опасных реакций:
Данные недоступны


ORGAL PST 100
Orgal PST 100 соответствует нормам по ЛОС, поэтапно отказывающимся от формальдегида, аммиака и других ограниченных веществ.


Тип продукта: Акрилы и акриловые сополимеры > Стирол/акриловые сополимеры
Химический состав: стирольно-акриловый сополимер.


Orgal PST 100 представляет собой сополимер стирола и акрила.
Orgal PST 100 подходит для глянцевых и текстурированных красок.
Orgal PST 100 рекомендуется для грунтовок, верхних покрытий EIFS, а также для внутренних и наружных работ, полуглянцевых красок с эффектом яичной скорлупы и красок для черепицы.


Orgal PST 100 соответствует нормам по ЛОС, поэтапно отказывающимся от формальдегида, аммиака и других ограниченных веществ.
Orgal PST 100 обладает хорошей стойкостью к истиранию благодаря высокой способности связывать пигменты, а также превосходной стойкости к щелочам и воде, что снижает выцветание.


Orgal PST 100 демонстрирует превосходную адгезию к минеральным основаниям и реологические характеристики при использовании загустителей на основе полиуретана.
Краски на основе Orgal PST 100 демонстрируют высокую стойкость цвета при колеровке универсальными красителями на водной основе.
Orgal PST 100 представляет собой стирол-акриловый сополимер, не содержащий APEO и аммиака, который образует прозрачные, твердые и блестящие пленки при высыхании при температуре выше 20°C.


Orgal PST 100 — связующее для красок, подходящее для большинства плоских и полуглянцевых красок, красок из ПВХ для внутренних и наружных работ из яичной скорлупы, толстослойных текстурированных, кварцевых и влагозащитных покрытий.
Максимальный срок хранения Оргал ПСТ 100 составляет 12 месяцев.



ИСПОЛЬЗОВАНИЕ И ПРИМЕНЕНИЕ ORGAL PST 100:
Orgal PST 100 подходит для глянцевых и текстурированных красок.
Orgal PST 100 рекомендуется для грунтовок, верхних покрытий EIFS, а также для внутренних и наружных работ, полуглянцевых красок с эффектом яичной скорлупы и красок для черепицы.
Orgal PST 100 соответствует нормам по ЛОС, поэтапно отказывающимся от формальдегида, аммиака и других ограниченных веществ.


Orgal PST 100 обладает хорошей стойкостью к истиранию благодаря высокой способности связывать пигменты, а также превосходной стойкости к щелочам и воде, что снижает выцветание.
Orgal PST 100 демонстрирует превосходную адгезию к минеральным основаниям и реологические характеристики при использовании загустителей на основе полиуретана.


Краски на основе Orgal PST 100 демонстрируют высокую стойкость цвета при колеровании универсальными красителями и красителями на водной основе.
Orgal PST 100 — связующее для красок, подходящее для большинства плоских и полуглянцевых красок, красок из ПВХ для внутренних и наружных работ из яичной скорлупы, толстослойных текстурированных, кварцевых и влагозащитных покрытий.



ФИЗИЧЕСКИЕ И ХИМИЧЕСКИЕ СВОЙСТВА ORGAL PST 100:
Тип продукта: Акрилы и акриловые сополимеры > Стирол/акриловые сополимеры
Химический состав: стирольно-акриловый сополимер.
Физическая форма: эмульсия, опал.



МЕРЫ ПЕРВОЙ ПОМОЩИ ОРГАЛА ПСТ 100:
-Описание мер первой помощи.
*Общие советы:
Покажите этот паспорт безопасности материала лечащему врачу.
*При вдыхании:
После ингаляции:
Свежий воздух.
*При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промыть кожу с
вода/душ.
*В случае зрительного контакта:
После зрительного контакта:
Промойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.
*При проглатывании:
После глотания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.
-Указание на необходимость немедленной медицинской помощи и специального лечения.
Данные недоступны



МЕРЫ ПРИ СЛУЧАЙНОМ ВЫБРОСЕ ORGAL PST 100:
-Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.
-Методы и материалы для локализации и очистки:
Закройте дренажи.
Соберите, свяжите и откачайте пролитую жидкость.
Соблюдайте возможные ограничения по материалам.
Возьмите в сухом виде.
Утилизируйте должным образом.
Очистите пораженный участок.



МЕРЫ ПОЖАРОТУШЕНИЯ ORGAL PST 100:
-Средства пожаротушения:
*Подходящие средства пожаротушения:
Углекислый газ (CO2)
Мыло
Сухой порошок
*Неподходящие средства пожаротушения:
Для этого вещества/смеси не установлены ограничения по огнетушащим веществам.
-Дальнейшая информация:
Не допускайте попадания воды для пожаротушения в поверхностные воды или систему грунтовых вод.



КОНТРОЛЬ ВОЗДЕЙСТВИЯ/ПЕРСОНАЛЬНАЯ ЗАЩИТА ORGAL PST 100:
-Параметры управления:
--Ингредиенты с параметрами контроля на рабочем месте:
-Средства контроля воздействия:
--Средства индивидуальной защиты:
*Защита глаз/лица:
Используйте средства защиты глаз.
Безопасные очки
*Защита тела:
защитная одежда
*Защита органов дыхания:
Рекомендуемый тип фильтра: Фильтр A
-Контроль воздействия на окружающую среду:
Не допускайте попадания продукта в канализацию.



ОБРАЩЕНИЕ И ХРАНЕНИЕ ORGAL PST 100:
-Условия безопасного хранения, включая любые несовместимости:
*Условия хранения:
Плотно закрыто.
Сухой.



СТАБИЛЬНОСТЬ И РЕАКЦИОННАЯ СПОСОБНОСТЬ ORGAL PST 100:
-Химическая стабильность:
Продукт химически стабилен при стандартных условиях окружающей среды (комнатная температура).
-Возможность опасных реакций:
Данные недоступны


Organik Hindistan Cevizi Yağı
COCONUT OIL ORGANIC VIRGIN; coconut oil; coconut palm oil; cocoanut oil; kokos oil; oils, coconut; fixed oil obtained by expression of the kernels of the seeds of the coconut, cocos nucifera l., palmaceae CAS NO:8001-31-8
Organik Katı Kakao Yağı
COCOA BUTTER ORGANIC ; Theobroma Cacao (Cocoa) Seed Butter; Cocoa, extract; THEOBROMA CACAO SEED BUTTER CAS NO:8002-31-1
ORP 5070
ORP 5070 ORP 5070 is a redispersible powder produced by drying an emulsion of Vinyl Acetate / VeoVa 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 5070 is used to modify mixtures containing hydraulic binders. Due to ORP 5070’s particular chemical / physical composition, ORP 5070 improves adhesion, flexibility and water resistance of ORP 5070 mortars containing hydraulic binders such as cement, gypsum or lime. Especially after heat aging and water immersion conditions ORP 5070 provides excellent performance. TYPICAL PROPERTIES OF ORP 5070 Appearance of ORP 5070 White powder Chemical composition of ORP 5070 VA / VeoVa Copolymer Stabilizing System of ORP 5070 PVOH Residual Humidity (%)of ORP 5070 Max. 1.5 Density (g/l) of ORP 5070 525 ± 75 Ash Content (%) of ORP 5070 12 ± 2 Alkali Resistance of ORP 5070 High After 1:1 Dispersion with Water 6.0 – 7.0 pH MFFT (°C) of ORP 5070 8 Due to strong adhesion properties of ORP 5070, ORP 5070 can be used for manufacturing of tile adhesives and EIFS adhesives fullfilling requirements of standarts. The recommended dosages: C1 tile adhesives of ORP 5070 : 0.5 – 1.0 % C2 tile adhesives of ORP 5070 : 2.0 – 5.0 % EIFS adhesives of ORP 5070: 1.0 – 2.0 % Having excellent adhesion properties of ORP 5070, abrassion and water resistance of ORP 5070, ORP 5070 can be used in tile grouts and repair mortar formulations, between 2.0 – 4.0 %. Because of providing excellent water resistance of ORP 5070 and compressive strength of ORP 5070 ORP 5070 can be used also in EIFS plaster formulations, between 3.0 – 5.0 %. ORP 5070 is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 5070 improves adhesion, ORP 5070 improves flexibility and ORP 5070 improves water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially after heat aging and in water immersion conditions, ORP 5070 provides excellent performance. ORP 5070 is used in Tile adhesives.ORP 5070 is used in Tile grouts and repair mortars.ORP 5070 is used in EIFS plasters.ORP 5070 is used in Adhesives fro EPS and XPS boards. ORP 5070 has excellent adhesion properties, ORP 5070 abrasion and water resistance, ORP 5070 can be used in tile joints and repair mortar formulations between 2.0 - 4.0%. Due to the excellent water resistance of ORP 5070 and the compressive strength of ORP 5070, ORP 5070 can be used in EIFS plaster formulations between 3.0 - 5.0%. ORP 5070 is used to modify mixtures containing hydraulic binders. ORP 5070 improves adhesion due to its unique chemical / physical composition, ORP 5070 increases flexibility and ORP 5070 increases the water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. ORP 5070 provides excellent performance especially after heat aging and immersion in water. ORP 5070 is used for tile adhesives, ORP 5070 for tile mortars and repair mortars, ORP 5070 for EIFS plasters, ORP 5070 for EPS and XPS boards. ORP 5070; is a redispersible powder produced by an emulsion of Vinyl Acetate / VeoVa copolymer with PVOH as a protective colloid. The specific chemical composition of the ORP 5070 polymer; allows the polymer to coalesce. ORP 5070 Provides good adhesion to re-dispersed polymer and cementitious substrates at low temperatures. ORP 5070 is used to modify mixtures containing hydraulic binders. Due to its special chemical / physical composition, ORP 5070; cement; adhesion of mortars containing hydraulic binders such as gypsum or lime; improves flexibility and water resistance. ORP 5070 offers excellent performance especially after heat aging and water immersion conditions. ORP 5070 is a ready-to-use, ORP 5070 fast drying, ORP 5070, water-based acrylic (VEOVA) copolymer floor and wall insulation primer with specific chemical and physical properties. ORP 5070 is an easy product to prepare for use. ORP 5070 It has excellent waterproofing. ORP 5070 Practical and easy to apply. ORP 5070 is water-based and environmentally friendly. ORP 5070 has high strength and UV resistance. ORP 5070 Provides the insulation of the walls and floors where it is applied, and allows breathing. ORP 5070 is used in floors, terraces and roofs that create wet areas and water ponding. ORP 5070 is used in foundation curtain concrete. ORP 5070 It is used as an adherence enhancing primer on the interior and exterior facades of buildings, on surfaces with adherence problems, before the product to be applied with the final layer. ORP 5070 It is used as an adherence enhancer before the screed to be applied on old concrete floors. ORP 5070 is used in factory warehouse areas. ORP 5070 is used for tile adhesives, ORP 5070 for tile mortars and repair mortars, ORP 5070 for EIFS plasters, ORP 5070 for EPS and XPS boards. ORP 5070 It is used on old surfaces with resistance problems. ORP 5070 is used as a protector on garden concrete and stone surfaces. ORP 5070 is used in sports fields with concrete and asphalt floors. Compounds modified with ORP 5070 VAE exhibit improved adhesion, flexural strength, deformability, wear resistance and are easier to process. Leveling, thixotropy and water retention are essentially unaffected. ORP 5070 is ideal for use with other mortar additives aimed at improving certain properties. ORP 5070 increases the adhesion between the base layer and the mortar, ORP 5070 makes the mortar with better alkali resistance. ORP 5070 Increases the compressive strength of the mortar, ORP 5070 extends the opening time. . ORP 5070 has excellent adhesion properties, ORP 5070 abrasion and water resistance, ORP 5070 can be used in tile joints and repair mortar formulations between 2.0 - 4.0%. Due to the excellent water resistance of ORP 5070 and the compressive strength of ORP 5070, ORP 5070 can be used in EIFS plaster formulations between 3.0 - 5.0%. ORP 5070 is used to modify mixtures containing hydraulic binders. ORP 5070 improves adhesion due to its unique chemical / physical composition, ORP 5070 increases flexibility and ORP 5070 increases the water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. ORP 5070 provides excellent performance especially after heat aging and immersion in water. ORP 5070 is used for tile adhesives, ORP 5070 is used as a protector on garden concrete and stone surfaces. ORP 5070 is used in sports fields with concrete and asphalt floors. Compounds modified with ORP 5070 VAE exhibit improved adhesion, flexural strength, deformability, wear resistance and are easier to process. Leveling, thixotropy and water retention are essentially unaffected. ORP 5070 is ideal for use with other mortar additives aimed at improving certain properties. ORP 5070 increases the adhesion between the base layer and the mortar, ORP 5070 makes the mortar with better alkali resistance. ORP 5070 is a redispersible powder produced by drying an emulsion of Vinyl Acetate / VeoVa 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 5070 is used to modify mixtures containing hydraulic binders. Due to ORP 5070’s particular chemical / physical composition, ORP 5070 improves adhesion, flexibility and water resistance of ORP 5070 mortars containing hydraulic binders such as cement, gypsum or lime. Especially after heat aging and water immersion conditions ORP 5070 provides excellent performance. TYPICAL PROPERTIES OF ORP 5070 Appearance of ORP 5070 White powder Chemical composition of ORP 5070 VA / VeoVa Copolymer Stabilizing System of ORP 5070 PVOH Residual Humidity (%)of ORP 5070 Max. 1.5 Density (g/l) of ORP 5070 525 ± 75 Ash Content (%) of ORP 5070 12 ± 2 Alkali Resistance of ORP 5070 High After 1:1 Dispersion with Water 6.0 – 7.0 pH MFFT (°C) of ORP 5070 8 Due to strong adhesion properties of ORP 5070, ORP 5070 can be used for manufacturing of tile adhesives and EIFS adhesives fullfilling requirements of standarts. The recommended dosages: C1 tile adhesives of ORP 5070 : 0.5 – 1.0 % C2 tile adhesives of ORP 5070 : 2.0 – 5.0 % EIFS adhesives of ORP 5070: 1.0 – 2.0 % Having excellent adhesion properties of ORP 5070, abrassion and water resistance of ORP 5070, ORP 5070 can be used in tile grouts and repair mortar formulations, between 2.0 – 4.0 %. Because of providing excellent water resistance of ORP 5070 and compressive strength of ORP 5070 ORP 5070 can be used also in EIFS plaster formulations, between 3.0 – 5.0 %. ORP 5070 is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 5070 improves adhesion, ORP 5070 improves flexibility and ORP 5070 improves water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially after heat aging and in water immersion conditions, ORP 5070 provides excellent performance. ORP 5070 is used in Tile adhesives.ORP 5070 is used in Tile grouts and repair mortars.ORP 5070 is used in EIFS plasters.ORP 5070 is used in Adhesives fro EPS and XPS boards. ORP 5070 has excellent adhesion properties, ORP 5070 abrasion and water resistance, ORP 5070 can be used in tile joints and repair mortar formulations between 2.0 - 4.0%. Due to the excellent water resistance of ORP 5070 and the compressive strength of ORP 5070, ORP 5070 can be used in EIFS plaster formulations between 3.0 - 5.0%. ORP 5070 is used to modify mixtures containing hydraulic binders. ORP 5070 improves adhesion due to its unique chemical / physical composition, ORP 5070 increases flexibility and ORP 5070 increases the water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. ORP 5070 provides excellent performance especially after heat aging and immersion in water. ORP 5070 is used for tile adhesives, ORP 5070 for tile mortars and repair mortars, ORP 5070 for EIFS plasters, ORP 5070 for EPS and XPS boards. ORP 5070; is a redispersible powder produced by an emulsion of Vinyl Acetate / VeoVa copolymer with PVOH as a protective colloid. The specific chemical composition of the ORP 5070 polymer; allows the polymer to coalesce. ORP 5070 Provides good adhesion to re-dispersed polymer and cementitious substrates at low temperatures. ORP 5070 is used to modify mixtures containing hydraulic binders. Due to its special chemical / physical composition, ORP 5070; cement; adhesion of mortars containing hydraulic binders such as gypsum or lime; improves flexibility and water resistance. ORP 5070 offers excellent performance especially after heat aging and water immersion conditions. ORP 5070 is a ready-to-use, ORP 5070 fast drying, ORP 5070, water-based acrylic (VEOVA) copolymer floor and wall insulation primer with specific chemical and physical properties. ORP 5070 is an easy product to prepare for use. ORP 5070 It has excellent waterproofing. ORP 5070 Practical and easy to apply. ORP 5070 is water-based and environmentally friendly. ORP 5070 has high strength and UV resistance. ORP 5070 Provides the insulation of the walls and floors where it is applied, and allows breathing. ORP 5070 is used in floors, terraces and roofs that create wet areas and water ponding. ORP 5070 is used in foundation curtain concrete. ORP 5070 It is used as an adherence enhancing primer on the interior and exterior facades of buildings, on surfaces with adherence problems, before the product to be applied with the final layer. ORP 5070 It is used as an adherence enhancer before the screed to be applied on old concrete floors. ORP 5070 is used in factory warehouse areas. ORP 5070 is used for tile adhesives, ORP 5070 for tile mortars and repair mortars, ORP 5070 for EIFS plasters, ORP 5070 for EPS and XPS boards. ORP 5070 It is used on old surfaces with resistance problems. ORP 5070 is used as a protector on garden concrete and stone surfaces. ORP 5070 is used in sports fields with concrete and asphalt floors. Compounds modified with ORP 5070 VAE exhibit improved adhesion, flexural strength, deformability, wear resistance and are easier to process. Leveling, thixotropy and water retention are essentially unaffected. ORP 5070 is ideal for use with other mortar additives aimed at improving certain properties. ORP 5070 increases the adhesion between the base layer and the mortar, ORP 5070 makes the mortar with better alkali resistance. ORP 5070 Increases the compressive strength of the mortar, ORP 5070 extends the opening time. . ORP 5070 has excellent adhesion properties, ORP 5070 abrasion and water resistance, ORP 5070 can be used in tile joints and repair mortar formulations between 2.0 - 4.0%. Due to the excellent water resistance of ORP 5070 and the compressive strength of ORP 5070, ORP 5070 can be used in EIFS plaster formulations between 3.0 - 5.0%. ORP 5070 is used to modify mixtures containing hydraulic binders. ORP 5070 improves adhesion due to its unique chemical / physical composition, ORP 5070 increases flexibility and ORP 5070 increases the water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. ORP 5070 provides excellent performance especially after heat aging and immersion in water. ORP 5070 is used for tile adhesives, ORP 5070 is used as a protector on garden concrete and stone surfaces. ORP 5070 is used in sports fields with concrete and asphalt floors. Compounds modified with ORP 5070 VAE exhibit improved adhesion, flexural strength, deformability, wear resistance and are easier to process. Leveling, thixotropy and water retention are essentially unaffected. ORP 5070 is ideal for use with other mortar additives aimed at improving certain properties. ORP 5070 increases the adhesion between the base layer and the mortar, ORP 5070 makes the mortar with better alkali resistance.
ORP 5070 MP
ORP 5070 MP ORP 5070 MP is a redispersible powder produced by drying an emulsion of Vinyl Acetate / VeoVa 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 5070 MP is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 5070 MP improves adhesion, flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially after heat aging and water immersion conditions ORP 5070 MP provides excellent performance. TYPICAL PROPERTIES Appearance White powder Chemical composition VA / VeoVa Copolymer Stabilizing System PVOH Residual Humidity (%) Max. 1.5 Density (g/l) 525 ± 75 Ash Content (%) 12 ± 2 Alkali Resistance High After 1:1 Dispersion with Water pH 6.0 – 7.0 MFFT (°C) 8 APPLICATION AREAS Adhesives: Due to its strong adhesion properties, ORP 5070 MP can be used for manufacturing of tile adhesives and EIFS adhesives fullfilling requirements of standarts. The recommended dosages: C1 tile adhesives : 0.5 – 1.0 % C2 tile adhesives : 2.0 – 5.0 % EIFS adhesives : 1.0 – 2.0 % Tile Grouts and Repair Mortars: Having excellent adhesion properties, abrassion and water resistance, ORP 5070 MP can be used in tile grouts and repair mortar formulations, between 2.0 – 4.0 %. EIFS Plasters: Because of providing excellent water resistance and compressive strength ORP 5070 MP can be used also in EIFS plaster formulations, between 3.0 – 5.0 % PRODUCT HANDLING – STORAGE – SHELFLIFE Packaging: Pallet with 18 or 30 paper bags, each 25 kg (450 or 750 kg) also 500 kg of big bags. Packages must be stored in a dry and cool warehouse at temperatures between 10 – 25 °C. 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. ORP 5070 MP 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 5070 MP is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 5070 MP improves adhesion, flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially in self levelling mortar formulations ORP 5070 MP provides excellent abrasion resistance, flexural & compressive stength and good leveling. APPLICATION AREAS of ORP 5070 MP ORP 5070 MP 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 5070 MP 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 5070 MP has to be used within 6 months after the date of delivery. ORP 5070 MP is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 5070 MP 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 5070 MP performs very well in transverse deformation conditions. APPLICATION AREAS of ORP 5070 MP ORP 5070 MP 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 5070 MP can be used with the ratio of 2.0 - 4.0 % in weight and without requiring an additional hydrophobic agent. Moreover ORP 5070 MP 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 5070 MP performs very well in cementitious exterior plasters and topcoats with the amunt of 2.0 - 4.0 %. PRODUCT HANDLING - STORAGE - SHELFLIFE of ORP 5070 MP 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. Product identifier Product name ORP 5070 MP Chemical name and synonym Vinyl Acetate l VeoVa l Acrylic terpolymer 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 5070 MP is an organic compound with the formula CH3CO2CH=CH2. This colorless liquid is the precursor to polyORP 5070 MP , an important industrial polymer. 1 Production of ORP 5070 MP 2 Preparation of ORP 5070 MP 2.1 Mechanism of ORP 5070 MP 2.2 Alternative routes 3 Polymerization of ORP 5070 MP 4 Other reactions of ORP 5070 MP 5 Toxicity evaluation of ORP 5070 MP Production of ORP 5070 MP The worldwide production capacity of ORP 5070 MP 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 5070 MP is the acetate ester of vinyl alcohol. Since vinyl alcohol is highly unstable (with respect to acetaldehyde), the preparation of ORP 5070 MP 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 5070 MP and a palladium hydride, which would be oxidized to give hydroxide. Polymerization It can be polymerized to give polyORP 5070 MP (PVA). With other monomers it can be used to prepare various copolymers such as ethylene-ORP 5070 MP (EVA), ORP 5070 MP -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 5070 MP 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 5070 MP undergoes transesterification, giving access to vinyl ethers: ROH + CH2=CHOAc → ROCH=CH2 + HOAc Toxicity evaluation Tests suggest that ORP 5070 MP 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 5070 MP 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 5070 MP 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 5070 MP in water contains 2.0-2.4 wt % ORP 5070 MP , whereas a saturated solution of water in ORP 5070 MP contains 0.9-1.0 wt % water; at 50 °C, the solubility of ORP 5070 MP in water is 0.1 wt % more than at 20 °C, but the solubility of water in ORP 5070 MP doubles to about 2 wt % The/ fate of inhaled ORP 5070 MP in rabbits /was studied/. ... ORP 5070 MP tended to remain in the body after it was inhaled; 70% of the ORP 5070 MP administered was retained, and an equilibrium was established in the first few min after exposure began. ... No ORP 5070 MP /was found/ in the blood, either during or after its inhalation, which suggested ... that ORP 5070 MP is rapidly metabolized when it enters the body through the lungs. Two male Wistar Rats exposed to ORP 5070 MP (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 5070 MP exposure levels exceeded 650 ppm (2320 mg/cu m). ORP 5070 MP 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 5070 MP 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 5070 MP and acetaldehyde by gas chromatography ... Acetaldehyde was found in expired air at all ORP 5070 MP exposure concentrations. With increasing the ORP 5070 MP exposure, concentration of acetaldehyde in expired air increased. At ORP 5070 MP 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 5070 MP (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 5070 MP 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 5070 MP 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 5070 MP is excreted as metabolites. On/ hydrolysis /in the blood/, ORP 5070 MP 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 5070 MP 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 5070 MP in vivo, rats were exposed in closed desiccator jar chambers, and gas uptake kinetics were studied. The decay of ORP 5070 MP was dose-dependent, indicating possible satn of metabolic pathway(s). The maximal clearance (at lower concn) of ORP 5070 MP from the system (30,000 mL/hr/kg) was similar to the maximal ventilation rate in this species. The exposure of rats to ORP 5070 MP 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 5070 MP (5.4 mM) revealed a rapid degradation of ORP 5070 MP and formation of acetaldehyde. During the 20 min observation period, no degradation of ORP 5070 MP or formation of acetaldehyde were observed in complete culture medium without blood, which suggested that the reaction was enzymatic. ORP 5070 MP 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 5070 MP 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 5070 MP 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 5070 MP and acetaldehyde were compared with data from the human nasal model simulation. For the ORP 5070 MP data a good fit was demonstrated (r = 0.9). The metabolism of ORP 5070 MP has been studied in animals ... ORP 5070 MP 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 5070 MP 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 5070 MP (200-2,000 ppm) in the air for 1.4 hours or less. The results show that ORP 5070 MP is rapidly metabolized by blood esterases and that hepatic monooxygenases have a minor role, if any, in the metabolism of ORP 5070 MP. In vitro metabolic studies show that ORP 5070 MP 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 5070 MP 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 5070 MP . The highest decrease (50%) in SH content was seen in guinea pigs following a single intraperitoneal injection of 500 mg/kg ORP 5070 MP . Glutathione conjugation may decrease the toxicity of potentially harmful electrophiles by facilitating excretion into the bile. These studies show that ORP 5070 MP 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 5070 MP 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 5070 MP may bind to various degrees with glutathione in different species, which may help to detoxify ORP 5070 MP or its metabolites and enhance their elimination. ORP 5070 MP 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 5070 MP metabolism not only takes place in the liver but also in several tissues. The half-life of /200 uM/ ORP 5070 MP 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 5070 MP through esterase-mediated metabolism. It is discussed that ORP 5070 MP exhibits its genotoxicity via acetaldehyde. For example /researchers/ demonstrated that ORP 5070 MP induces /DNA protein crosslinking/ via acetaldehyde, and ... chromosomal damage induced by ORP 5070 MP 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 5070 MP is primarily used as a monomer in the production of polyORP 5070 MP and polyvinyl alcohol. Its chief use is as a monomer for making poly(ORP 5070 MP ) and ORP 5070 MP 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 5070 MP 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 5070 MP has been used primarily to produce polyORP 5070 MP emulsions and polyvinyl alcohol. The principle use of these emulsions has been in adhesives, paints, textiles, and paper products. PRODUCT PROFILE: ORP 5070 MP : PolyORP 5070 MP accounts for about 48% of ORP 5070 MP 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 5070 MP (EVA) polymers, ethylene vinyl alcohol (EVOH) barrier resins. PRODUCT PROFILE: ORP 5070 MP : ORP 5070 MP monomer's (VAM) main use is polyORP 5070 MP 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 5070 MP (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 5070 MP : ORP 5070 MP monomer (VAM) is mainly used in polyORP 5070 MP 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 5070 MP (EVA) polymers, ethylene vinyl alcohol (EVOH) barrier resins and polyvinyl butyral (PVB). CHEMICAL PROFILE: ORP 5070 MP . PolyORP 5070 MP emulsions and resins, 40%; (this area is divided evenly between paints and adhesives); polyvinyl alcohol, 15%; polyvinyl butyral, 8%; ethylene-ORP 5070 MP resins, 6%; polyvinyl chloride copolymers, 3%; miscellaneous, 1%; exports, 27%. CHEMICAL PROFILE: ORP 5070 MP : PolyORP 5070 MP emulsions and resins, 57%; polyvinyl alcohol, 19%; polyvinyl butyral, 10%; ethylene-ORP 5070 MP resins, 8%; ethylene vinyl alcohol, 2%; miscellaneous, including polyvinyl chloride copolymers, 4%. PRODUCT FOCUS: ORP 5070 MP Monomer (VAM): Global Demand: 2003: 4.3 million tonnes. PolyORP 5070 MP , 44%; polyORP 5070 MP , 40%; ethylene vinyl alcohol, 12%. ORP 5070 MP , acetic anhydride, ethanol, methanol, and formaldehyde were formed in aq extracts of polyORP 5070 MP films only in some cases and in insignificant quantities. The difference between pH of aq extracts of polyORP 5070 MP 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 5070 MP film extracts and up to 12.3 mg bromide/L in inactivated extracts. The oxidizability of the polyORP 5070 MP 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 5070 MP . 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 5070 MP 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 5070 MP has satisfactory properties for medicinal use. ORP 5070 MP 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 5070 MP 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 5070 MP is also used as a coating in plastic films for food packaging and as a modifier of food starch. ORP 5070 MP is primarily used as a monomer in the production of polyORP 5070 MP and polyvinyl alcohol. Acute (short-term) inhalation exposure of workers to ORP 5070 MP 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 5070 MP 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 5070 MP for carcinogenicity. ORP 5070 MP 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 5070 MP (427 °C) shall be used in ORP 5070 MP storage areas. The storage of ORP 5070 MP in glass containers should not be in the same areas as oxidizing agents or other incompatible chemicals. Containers of ORP 5070 MP 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 5070 MP . There is limited evidence in experimental animals for the carcinogenicity of ORP 5070 MP . Overall evaluation: ORP 5070 MP is possibly carcinogenic to humans (Group 2B). In making the overall evaluation, the working group took into account the following evidence: (1) ORP 5070 MP 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 5070 MP and acetaldehyde induce nasal cancer in rats after administration by inhalation. (3) ORP 5070 MP 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 5070 MP 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 5070 MP 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 5070 MP in both tissue types. Semicarbazide, an aldehyde scavenger, was unable to protect the tissues from ORP 5070 MP -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 5070 MP 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 5070 MP during resting and light exercise at three exposure levels (1, 5 and 10 ppm nominally). Both, labeled ORP 5070 MP 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 0.8 sec in an exposure period of 2 to 5 min resulting in data during all phases of the breathing. The rate of sampling was rapid enough to capture much of the behavior of ORP 5070 MP in the human nasal cavity including inhalation and exhalation. However, the sampling was not frequent enough to accurately capture the peak concentration in every breath. ORP 5070 MP 's production and use as a monomer for making poly (ORP 5070 MP) and ORP 5070 MP copolymers, in the production of paints, sealants, coatings, and binders and in miscellaneous uses such as chewing gum and tablet coatings may result in its release to the environment through various waste streams. If released to air, a vapor pressure of 90.2 mm Hg at 20 °C indicates ORP 5070 MP will exist solely as a vapor in the ambient atmosphere. Vapor-phase ORP 5070 MP is expected to be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 14 hours. If released to soil, ORP 5070 MP is expected to have high mobility based upon an estimated Koc of 60. Although leaching is possible, concurrent hydrolysis will decrease its importance. Volatilization from moist soil surfaces is also expected to be an important fate process based upon an estimated Henry's Law constant of 5.1X10-4 atm-cu m/mole. ORP 5070 MP may volatilize from dry soil surfaces based upon its vapor pressure. Polymerization may occur in sunlight. Biodegradation of ORP 5070 MP may be an important environmental fate process in soil under both aerobic (51 to 62% biodegradation reached in 5 day BOD test using sewage inoculum) and anaerobic conditions (nearly complete degradation in 26 hrs); reaction products of acetaldehyde and acetate are formed under both oxygen conditions. If released to water, ORP 5070 MP is not expected to adsorb to suspended solids and sediment in water based on the estimated Koc value. Volatilization from water surfaces is expected to be an important fate process based on its estimated Henry's Law constant. Estimated volatilization half-lives for a model river and model lake are 4 hours and 4 days, respectively. A 98% of theoretical BOD was reported using activated sludge in the Japanese MITI test, suggesting that biodegradation may be an important environmental fate process in water. An estimated BCF of 3.2 suggests the potential for bioconcentration in aquatic organisms is low. Degradation by hydrolysis (half-life of 7.3 days at 25 °C and pH 7) and by photochemically produced oxidants will occur. Occupational exposure to ORP 5070 MP may occur through inhalation and dermal contact with this compound at workplaces where ORP 5070 MP is produced or used. The general population may be exposed to ORP 5070 MP through inhalation and dermal contact with products containing ORP 5070 MP ; limited exposure may occur via ingestion from its use in chewing gum and tablet coatings. (SRC) ORP 5070 MP 's production and use as a monomer for making poly(ORP 5070 MP ) and ORP 5070 MP copolymers, in the production of paints, films, sealants, lacquers, coatings, food packaging, and binders, in chewing gum and as a tablet coating(1,2) and safety glass(3) may result in its releas
ORP 5070 MP
ORP 5070 MP: Redispersible Powder for Dry-Mix Mortars. ORP 5070 MP is a redispersible powder produced by drying an emulsion of Vinyl Acetate / VeoVa 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 5070 MP is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 5070 MP improves adhesion, flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially after heat aging and water immersion conditions ORP 5070 MP provides excellent performance. TYPICAL PROPERTIES Appearance: White powder Chemical composition:VA / VeoVa Copolymer Stabilizing System:PVOH Residual Humidity (%):Max. 1.5 Density (g/l):525 ± 75 Ash Content (%):12 ± 2 Alkali Resistance:High After 1:1 Dispersion with Water pH: 6.0 – 7.0 MFFT (°C):8 APPLICATION AREAS Adhesives: Due to its strong adhesion properties, ORP 5070 MP can be used for manufacturing of tile adhesives and EIFS adhesives fullfilling requirements of standarts. The recommended dosages: C1 tile adhesives : 0.5 – 1.0 % C2 tile adhesives : 2.0 – 5.0 % EIFS adhesives : 1.0 – 2.0 % Tile Grouts and Repair Mortars: Having excellent adhesion properties, abrassion and water resistance, ORP 5070 MP can be used in tile grouts and repair mortar formulations, between 2.0 – 4.0 %. EIFS Plasters: Because of providing excellent water resistance and compressive strength ORP 5070 MP can be used also in EIFS plaster formulations, between 3.0 – 5.0 % PRODUCT HANDLING – STORAGE – SHELFLIFE Packaging: Pallet with 18 or 30 paper bags, each 25 kg (450 or 750 kg) also 500 kg of big bags. Packages must
ORP 5377 HP
ORP 5377 HP:Hydrophobic Redispersible Powder for Dry-Mix Mortars. ORP 5377 HP is a redispersible powder produced by drying an emulsion of Vinyl Acetate / Vinyl Versatate 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 5377 HP is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 5377 HP improves adhesion, abrasion resistance,flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially for water repellency, abrasion resistance and mechanical performance tests after water immerison, ORP 5377 HP provides excellent performance. TYPICAL PROPERTIES Appearance: White powder Chemical composition: VA/VV 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):9 ±1 APPLICATION AREAS Tile Grouts and Repair Mortars: Having excellent adhesion properties, abrassion and water resistance, ORP 5377 HP can be used in tile grouts and repair mortar formulations, between 2.0 – 4.0 %. ETICS (Exterior Thermal Insulation Coating Systems) Plasters: Because of providing excellent water resistance and compressive strength ORP 5377 HP can be used also in ETICS plaster formulations, between 3.0 – 5.0 % 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 6072 MP
ORP 6072 MP Redispersible Powder for Dry-Mix Mortars INTRODUCTION ORP 6072 MP is a redispersible powder produced by drying an emulsion of Vinyl Acetate / VeoVa / 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 to cementitious substrates. ORP 6072 MP is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 6072 MP improves adhesion, flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially after heat aging and water immersion conditions ORP 6072 MP provides excellent performance. TYPICAL PROPERTIES Appearance : White powder Chemical composition: VA / VeoVa / Acrylic Terpolymer Stabilizing System: PVOH Residual Humidity (%):Max. 2.0 Bulk Density (g/l):400 – 600 Ash Content (%):14 ± 2 Alkali Resistance: High After 1:1 Dispersion with Water MFFT (°C): 8 ±1 APPLICATION AREAS Adhesives: Due to its strong adhesion properties, ORP 6072 MP can be used for manufacturing of tile adhesives and ETICS adhesives fullfilling requirements of standarts. The recommended dosages: C1 tile adhesives : 0.5 – 1.0 % C2 tile adhesives : 2.0 – 5.0 % ETICS adhesives : 1.0 – 2.0 % Tile Grouts and Repair Mortars: Having excellent adhesion properties, abrasion and water resistance, ORP 6072 MP can be used in tile grouts and repair mortar formulations, between 2.0 – 4.0 %. ETICS (Exterior Thermal Insulation Coating Systems) Plasters: Because of providing excellent water resistance and compressive strength ORP 6072 MP can be used also in ETICS plaster formulations, between 3.0 – 5.0 % 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 7085 HM
ORP 7085 HM Redispersible Powder for Dry-Mix Mortars ORP 7085 HM is a redispersible powder produced by drying an emulsion of VAM / 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 7085 HM is used to modify mixtures containing hydraulic binders. Due to its particular chemical /physical composition, ORP 7085 HM improves adhesion, flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. TYPICAL PROPERTIES Appearance: White powder Chemical composition: VAM / Acrylic Copolymer Stabilizing System: PVOH Residual Humidity: ~1 % Density (g/l): 525 ± 75 Ash Content % ± 2: 11 Alkali Resistance :High After 1:1 Dispersion with Water pH : 6.0 – 7.0 MFFT (°C):7 APPLICATION AREAS Tile Adhesives: Due to its strong adhesion properties, ORP 7085 HM can be used for manufacturing of tile adhesives fullfilling C1 & C2 requirements. The recommended dosages: C1 tile adhesives: 0.5 – 1.0 % C2 tile adhesives: 1.0 – 3.0 % Repair Mortars: Having excellent adhesion properties, abrassion and water resistance, ORP 7085 HM can be used between 1.0 – 2.0 % in repair mortar formulations. PRODUCT HANDLING – STORAGE – SHELFLIFE Packaging: Pallet with 18 paper bags, each 25 kg (450 kg) or big bags (500 kg). Packages must be stored in a dry and cool warehouse at temperatures between 10 – 25 °C. 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.
ORP 7085 HM
ORP 7085 HM ORP 7085 HM is a redispersible powder produced by drying an emulsion of VAM / 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 7085 HM is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 7085 HM improves adhesion, flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. TYPICAL PROPERTIES Appearance White powder Chemical composition VAM / Acrylic Copolymer Stabilizing System PVOH Residual Humidity ~1 % Density (g/l) 525 ± 75 Ash Content % ± 2 11 Alkali Resistance High After 1:1 Dispersion with Water pH 6.0 – 7.0 MFFT (°C) 7 APPLICATION AREAS Tile Adhesives: Due to its strong adhesion properties, ORP 7085 HM can be used for manufacturing of tile adhesives fullfilling C1 & C2 requirements. The recommended dosages: C1 tile adhesives: 0.5 – 1.0 % C2 tile adhesives: 1.0 – 3.0 % Repair Mortars: Having excellent adhesion properties, abrassion and water resistance, ORP 7085 HM can be used between 1.0 – 2.0 % in repair mortar formulations. PRODUCT HANDLING – STORAGE – SHELFLIFE Packaging: Pallet with 18 paper bags, each 25 kg (450 kg) or big bags (500 kg). Packages must be stored in a dry and cool warehouse at temperatures between 10 – 25 °C. 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. ORP 7085 HM 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 7085 HM is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 7085 HM improves adhesion, flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially in self levelling mortar formulations ORP 7085 HM provides excellent abrasion resistance, flexural & compressive stength and good leveling. APPLICATION AREAS of ORP 7085 HM ORP 7085 HM 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 7085 HM 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 7085 HM has to be used within 6 months after the date of delivery. ORP 7085 HM is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 7085 HM 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 7085 HM performs very well in transverse deformation conditions. APPLICATION AREAS of ORP 7085 HM ORP 7085 HM 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 7085 HM can be used with the ratio of 2.0 - 4.0 % in weight and without requiring an additional hydrophobic agent. Moreover ORP 7085 HM 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 7085 HM performs very well in cementitious exterior plasters and topcoats with the amunt of 2.0 - 4.0 %. PRODUCT HANDLING - STORAGE - SHELFLIFE of ORP 7085 HM 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 7085 HM 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 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 7085 HM is an organic compound with the formula CH3CO2CH=CH2. This colorless liquid is the precursor to polyORP 7085 HM , an important industrial polymer. 1 Production of ORP 7085 HM 2 Preparation of ORP 7085 HM 2.1 Mechanism of ORP 7085 HM 2.2 Alternative routes 3 Polymerization of ORP 7085 HM 4 Other reactions of ORP 7085 HM 5 Toxicity evaluation of ORP 7085 HM Production of ORP 7085 HM The worldwide production capacity of ORP 7085 HM 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 7085 HM is the acetate ester of vinyl alcohol. Since vinyl alcohol is highly unstable (with respect to acetaldehyde), the preparation of ORP 7085 HM 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 7085 HM and a palladium hydride, which would be oxidized to give hydroxide. Polymerization It can be polymerized to give polyORP 7085 HM (PVA). With other monomers it can be used to prepare various copolymers such as ethylene-ORP 7085 HM (EVA), ORP 7085 HM -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 7085 HM 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 7085 HM undergoes transesterification, giving access to vinyl ethers: ROH + CH2=CHOAc → ROCH=CH2 + HOAc Toxicity evaluation Tests suggest that ORP 7085 HM 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 7085 HM 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 7085 HM 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 7085 HM in water contains 2.0-2.4 wt % ORP 7085 HM , whereas a saturated solution of water in ORP 7085 HM contains 0.9-1.0 wt % water; at 50 °C, the solubility of ORP 7085 HM in water is 0.1 wt % more than at 20 °C, but the solubility of water in ORP 7085 HM doubles to about 2 wt % The/ fate of inhaled ORP 7085 HM in rabbits /was studied/. ... ORP 7085 HM tended to remain in the body after it was inhaled; 70% of the ORP 7085 HM administered was retained, and an equilibrium was established in the first few min after exposure began. ... No ORP 7085 HM /was found/ in the blood, either during or after its inhalation, which suggested ... that ORP 7085 HM is rapidly metabolized when it enters the body through the lungs. Two male Wistar Rats exposed to ORP 7085 HM (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 7085 HM exposure levels exceeded 650 ppm (2320 mg/cu m). ORP 7085 HM 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 7085 HM 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 7085 HM and acetaldehyde by gas chromatography ... Acetaldehyde was found in expired air at all ORP 7085 HM exposure concentrations. With increasing the ORP 7085 HM exposure, concentration of acetaldehyde in expired air increased. At ORP 7085 HM 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 7085 HM (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 7085 HM 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 7085 HM 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 7085 HM is excreted as metabolites. On/ hydrolysis /in the blood/, ORP 7085 HM 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 7085 HM 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 7085 HM in vivo, rats were exposed in closed desiccator jar chambers, and gas uptake kinetics were studied. The decay of ORP 7085 HM was dose-dependent, indicating possible satn of metabolic pathway(s). The maximal clearance (at lower concn) of ORP 7085 HM from the system (30,000 mL/hr/kg) was similar to the maximal ventilation rate in this species. The exposure of rats to ORP 7085 HM 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 7085 HM (5.4 mM) revealed a rapid degradation of ORP 7085 HM and formation of acetaldehyde. During the 20 min observation period, no degradation of ORP 7085 HM or formation of acetaldehyde were observed in complete culture medium without blood, which suggested that the reaction was enzymatic. ORP 7085 HM 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 7085 HM 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 7085 HM 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 7085 HM and acetaldehyde were compared with data from the human nasal model simulation. For the ORP 7085 HM data a good fit was demonstrated (r = 0.9). The metabolism of ORP 7085 HM has been studied in animals ... ORP 7085 HM 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 7085 HM 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 7085 HM (200-2,000 ppm) in the air for 1.4 hours or less. The results show that ORP 7085 HM is rapidly metabolized by blood esterases and that hepatic monooxygenases have a minor role, if any, in the metabolism of ORP 7085 HM. In vitro metabolic studies show that ORP 7085 HM 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 7085 HM 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 7085 HM . The highest decrease (50%) in SH content was seen in guinea pigs following a single intraperitoneal injection of 500 mg/kg ORP 7085 HM . Glutathione conjugation may decrease the toxicity of potentially harmful electrophiles by facilitating excretion into the bile. These studies show that ORP 7085 HM 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 7085 HM 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 7085 HM may bind to various degrees with glutathione in different species, which may help to detoxify ORP 7085 HM or its metabolites and enhance their elimination. ORP 7085 HM 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 7085 HM metabolism not only takes place in the liver but also in several tissues. The half-life of /200 uM/ ORP 7085 HM 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 7085 HM through esterase-mediated metabolism. It is discussed that ORP 7085 HM exhibits its genotoxicity via acetaldehyde. For example /researchers/ demonstrated that ORP 7085 HM induces /DNA protein crosslinking/ via acetaldehyde, and ... chromosomal damage induced by ORP 7085 HM 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 7085 HM is primarily used as a monomer in the production of polyORP 7085 HM and polyvinyl alcohol. Its chief use is as a monomer for making poly(ORP 7085 HM ) and ORP 7085 HM 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 7085 HM 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 7085 HM has been used primarily to produce polyORP 7085 HM emulsions and polyvinyl alcohol. The principle use of these emulsions has been in adhesives, paints, textiles, and paper products. PRODUCT PROFILE: ORP 7085 HM : PolyORP 7085 HM accounts for about 48% of ORP 7085 HM 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 7085 HM (EVA) polymers, ethylene vinyl alcohol (EVOH) barrier resins. PRODUCT PROFILE: ORP 7085 HM : ORP 7085 HM monomer's (VAM) main use is polyORP 7085 HM 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 7085 HM (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 7085 HM : ORP 7085 HM monomer (VAM) is mainly used in polyORP 7085 HM 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 7085 HM (EVA) polymers, ethylene vinyl alcohol (EVOH) barrier resins and polyvinyl butyral (PVB). CHEMICAL PROFILE: ORP 7085 HM . PolyORP 7085 HM emulsions and resins, 40%; (this area is divided evenly between paints and adhesives); polyvinyl alcohol, 15%; polyvinyl butyral, 8%; ethylene-ORP 7085 HM resins, 6%; polyvinyl chloride copolymers, 3%; miscellaneous, 1%; exports, 27%. CHEMICAL PROFILE: ORP 7085 HM : PolyORP 7085 HM emulsions and resins, 57%; polyvinyl alcohol, 19%; polyvinyl butyral, 10%; ethylene-ORP 7085 HM resins, 8%; ethylene vinyl alcohol, 2%; miscellaneous, including polyvinyl chloride copolymers, 4%. PRODUCT FOCUS: ORP 7085 HM Monomer (VAM): Global Demand: 2003: 4.3 million tonnes. PolyORP 7085 HM , 44%; polyORP 7085 HM , 40%; ethylene vinyl alcohol, 12%. ORP 7085 HM , acetic anhydride, ethanol, methanol, and formaldehyde were formed in aq extracts of polyORP 7085 HM films only in some cases and in insignificant quantities. The difference between pH of aq extracts of polyORP 7085 HM 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 7085 HM film extracts and up to 12.3 mg bromide/L in inactivated extracts. The oxidizability of the polyORP 7085 HM 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 7085 HM . 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 7085 HM 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 7085 HM has satisfactory properties for medicinal use. ORP 7085 HM 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 7085 HM 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 7085 HM is also used as a coating in plastic films for food packaging and as a modifier of food starch. ORP 7085 HM is primarily used as a monomer in the production of polyORP 7085 HM and polyvinyl alcohol. Acute (short-term) inhalation exposure of workers to ORP 7085 HM 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 7085 HM 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 7085 HM for carcinogenicity. ORP 7085 HM 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 7085 HM (427 °C) shall be used in ORP 7085 HM storage areas. The storage of ORP 7085 HM in glass containers should not be in the same areas as oxidizing agents or other incompatible chemicals. Containers of ORP 7085 HM 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 7085 HM . There is limited evidence in experimental animals for the carcinogenicity of ORP 7085 HM . Overall evaluation: ORP 7085 HM is possibly carcinogenic to humans (Group 2B). In making the overall evaluation, the working group took into account the following evidence: (1) ORP 7085 HM 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 7085 HM and acetaldehyde induce nasal cancer in rats after administration by inhalation. (3) ORP 7085 HM 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 7085 HM 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 7085 HM 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 7085 HM in both tissue types. Semicarbazide, an aldehyde scavenger, was unable to protect the tissues from ORP 7085 HM -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 7085 HM 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 7085 HM during resting and light exercise at three exposure levels (1, 5 and 10 ppm nominally). Both, labeled ORP 7085 HM 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 0.8 sec in an exposure period of 2 to 5 min resulting in data during all phases of the breathing. The rate of sampling was rapid enough to capture much of the behavior of ORP 7085 HM in the human nasal cavity including inhalation and exhalation. However, the sampling was not frequent enough to accurately capture the peak concentration in every breath. ORP 7085 HM 's production and use as a monomer for making poly (ORP 7085 HM) and ORP 7085 HM copolymers, in the production of paints, sealants, coatings, and binders and in miscellaneous uses such as chewing gum and tablet coatings may result in its release to the environment through various waste streams. If released to air, a vapor pressure of 90.2 mm Hg at 20 °C indicates ORP 7085 HM will exist solely as a vapor in the ambient atmosphere. Vapor-phase ORP 7085 HM is expected to be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 14 hours. If released to soil, ORP 7085 HM is expected to have high mobility based upon an estimated Koc of 60. Although leaching is possible, concurrent hydrolysis will decrease its importance. Volatilization from moist soil surfaces is also expected to be an important fate process based upon an estimated Henry's Law constant of 5.1X10-4 atm-cu m/mole. ORP 7085 HM may volatilize from dry soil surfaces based upon its vapor pressure. Polymerization may occur in sunlight. Biodegradation of ORP 7085 HM may be an important environmental fate process in soil under both aerobic (51 to 62% biodegradation reached in 5 day BOD test using sewage inoculum) and anaerobic conditions (nearly complete degradation in 26 hrs); reaction products of acetaldehyde and acetate are formed under both oxygen conditions. If released to water, ORP 7085 HM is not expected to adsorb to suspended solids and sediment in water based on the estimated Koc value. Volatilization from water surfaces is expected to be an important fate process based on its estimated Henry's Law constant. Estimated volatilization half-lives for a model river and model lake are 4 hours and 4 days, respectively. A 98% of theoretical BOD was reported using activated sludge in the Japanese MITI test, suggesting that biodegradation may be an important environmental fate process in water. An estimated BCF of 3.2 suggests the potential for bioconcentration in aquatic organisms is low. Degradation by hydrolysis (half-life of 7.3 days at 25 °C and pH 7) and by photochemically produced oxidants will occur. Occupational exposure to ORP 7085 HM may occur through inhalation and dermal contact with this compound at workplaces where ORP 7085 HM is produced or used. The general population may be exposed to ORP 7085 HM through inhalation and dermal contact with products containing ORP 7085 HM ; limited exposure may occur via ingestion from its use in chewing gum and tablet coatings. (SRC) ORP 7085 HM 's production and use as a monomer for making poly(ORP 7085 HM ) and ORP 7085 HM copolymers, in the production of paints, films, sealants, lacquers, coatings, food packaging, and binders, in chewing gum and as a tablet coating(1,2) and safety glass(3) may result in its release to the environment through various waste streams(SRC). ORP 7085 HM can be released to the environment from industrial sources and biomass combustion(4). Waste gases from scrubbers (generated during the industrial manufacture of ORP 7085 HM ) may contain trace levels of ORP 7085 HM (5). TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 60(
ORP 7099 RD
ORP 7099 RD Introduction: ORP 7099 RD is a redispersible powder obtained by drying an emulsion of a vinyl acetate / VeoVa / acrylic terpolymer 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 7099 RD is used for modification of mixtures containing hydraulic binders. Due to its special chemical / physical composition, ORP 7099 RD improves the adhesion, elasticity and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Properties: Appearance - White powder Chemical composition - Vinyl acetate / VeoVa / acrylic terpolymer Stabilizing system - PVA Residual moisture (%) - Max. 1.5 Density (g / l) - 400 - 600 Ash residue (%) - 12 ± 2 Alkaline resistance - High After dispersion with water - 1: 1 pH - 6.0-7.0 Minimum film formation temperature (ºС) - 0 Applications: C1 tile adhesives: Recommended dosages: 0.5-1.0% C2 tile adhesives: Recommended dosages: 2.0-5.0% Repair mortars: With excellent adhesion, resistance and water resistance, ORP 7099 RD can be used in repair mortar formulations at a dosage of 1.0 - 2.0%. Storage and expiration date: 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 temperatures between 10 - 25 ° C. It is not advisable to stack 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.
ORP 7365
ORP 7365 HP-Hydrophobic Redispersible Powder for Dry-Mix Mortars.ORP 7365 HP 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 7365 HP is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 7365 HP improves adhesion, abrasion resistance,flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially in the systems that require water resistance, flexibility and abrasion resistance at the same time ORP 7365 HP provides excellent performance.Having excellent abrasion resistance, flexibility and water resistance ORP 7365 HP can be used in tile grouts formulations, between 2.0 – 4.0 %.Because of providing excellent water resistance, flexibility and compressive strength ORP 7365 HP can be used also in EIFS plaster formulations, between 3.0 – 5.0 %.Water Proofing Mortars:ORP 7365 HP can be used in one component water proofing mortars, between 7.0 – 10.0% because of having excellent flexibility, hydrophobicity and water resistance.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 substraHtes.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is used to modify mixtures containing hydraulic binders. Due to ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) s particular chemical / physical composition,ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) improves adhesion, abrasion resistance,flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially in the systems ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) require water resistance, flexibility and abrasion resistance at the same time ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) provides excellent performance.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) Application Areas: ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) having excellent abrasion resistance, flexibility and water resistance ORP 7365 HP can be used in tile grouts formulations, between 2.0 - 4.0 %.Because of providing excellent water resistance, flexibility and compressive strength ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) can be used also in EIFS plaster formulations, between 3.0 - 5.0 %. ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) Product; Handling; Storage ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) Packaging: Pallet with 18 or 30 paper bags, each 25 kg (450 or 750 kg) also 500 kg of big bags.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) Packages must be stored in a dry and cool warehouse at temperatures between 10 - 25 °C. Pallets must not be stacked on top of each other to avoid caking due to the thermoplasticity of the polymer.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) Packing must be closed well after usage for protection against humidity and caking.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) has to be used within 6 months.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is a redispersible powder obtained by drying a Vinyl Acetate / Acrylic copolymer emulsion with PVA as a protective colloid. The chemical composition of the polymer ensures the coalescence of the redispersible polymer at low temperatures and provides good adhesion to mineral substrates. ORP 7365 HP is used for modifying mixtures containing various binders. Due to its special physical / chemical composition, ORP 7365 HP improves adhesion, abrasion resistance, elasticity and water resistance of mortars.Due to ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer)s excellent water resistance, elasticity and compressive strength,ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) can be used for plasters in SPTC.ith excellent abrasion, flexibility and water resistance,ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) can be used in tile grouting compounds.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is a redispersible powder obtained by drying a Vinyl Acetate / Acrylic copolymer emulsion with PVA as a protective colloid. The chemical composition of the polymer ensures the coalescence of the redispersible polymer at low temperatures and provides good adhesion to mineral substrates. ORP 7365 HP is used for modifying mixtures containing various binders. Due to its special physical / chemical composition, ORP 7365 HP improves adhesion, abrasion resistance, elasticity and water resistance of mortars.Due to ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer)s excellent water resistance, elasticity and compressive strength, ORP 7365 HP can be used for plasters in SPTC.Due to ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer)s excellent flexibility, hydrophobicity and water resistance, ORP 7365 HP can be used in one-component waterproofing mortars.With excellent abrasion, flexibility and water resistance,ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) can be used in tile grouting compounds.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 7365 HP (Vinyl Acetate,Acrylic Copolymer) is used to modify mixtures containing hydraulic binders. Due to ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer)s particular chemical / physical composition,ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) improves adhesion, abrasion resistance,flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially in the systems ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) require water resistance, flexibility and abrasion resistance at the same time ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) provides excellent performance.Having excellent abrasion resistance, flexibility and water resistance ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) can be used in tile grouts formulations, between 2.0 - 4.0 %.Because of providing excellent water resistance, flexibility and compressive strength ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) can be used also in EIFS plaster formulations, between 3.0 - 5.0 %.Water Proofing Mortars: ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) can be used in one component water proofing mortars, between 7.0 - 10.0% because of having excellent flexibility, hydrophobicity and water resistance.The polymer powder based vinylatsetatnoho-acrylic copolymer ORP 7099 RD (net weight 12600 kg), ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) (net weight 450 kg) taORP THERMOBOND 74 (net weight 7,200 kg) is redysperhovanyy powder obtained by drying emulsion acrylic vinylatsetatnoho terpolimeraz polivinylovym alcohol in yakostizahysnoho colloid. The structure of ORP 7099 RD are: vinyl acetate monomer - 89% butyl acrylate monomer - 8%, the agent antizlezhuvannya - 1% filler - 1%, other functional additives - 1% final humidity - max 2% Bottom ash residue - 12 + -2%. The structure of ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) include: vinyl acetate monomer - 91% butyl acrylate monomer - 5% agent antizlezhuvannya - 1% filler - 1%, other functional additives - 1% final humidity - max 2% Bottom ash residue - 14 + -2%.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is a hydrophobic polymer powder. Used in systems requiring water resistance, flexibility and abrasion resistance.K proofing Mortar Formulation Powder CEM II 4,5R -8 µm Silica Sand Tylose MH 6 YP4 ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) Floset AD Filler Retention Agent Performance Modifier Plasticizer Shin-Etsu SNF Liquid Agitan 3 Acticide MV Defoamer Biocide Münzing Chemie Thor *Powder: Liquid ratio is : in weight.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is an organic compound with the formula CH3CO2CH=CH2.This colorless liquid is the precursor to polyvinyl acetate, an important industrial polymer.The worldwide production capacity of ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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).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%).ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is a key ingredient in furniture glue.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is the acetate ester of vinyl alcohol. Since vinyl alcohol is highly unstable (with respect to acetaldehyde), the preparation of ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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.The main side reaction is the combustion of organic precursors.Isotope labeling and kinetics experiments suggest that the mechanism involves PdCH2CH2OAc-containing intermediates. Beta-hydride elimination would generate vinyl acetate and a palladium hydride, which would be oxidized to give hydroxide.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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, vinyl acetate was first prepared by Fritz Klatte in 1912.[3] Another route to vinyl acetate involves thermal decomposition of ethylidene diacetate.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) can be polymerized to give polyvinyl acetate (PVA). With other monomers it can be used to prepare various copolymers such as ethylene-vinyl acetate (EVA), ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) (VA/AA), polyvinyl chloride acetate (PVCA), and polyvinylpyrrolidone (Vp/Va Copolymer, used in hair gels).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.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) undergoes transesterification with a variety of carboxylic acids.The alkene also undergoes Diels-Alder and 2+2 cycloadditions.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) undergoes transesterification, giving access to vinyl ethers.Tests suggest that ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is of low toxicity. For rats (oral) LD50 is 2920 mg/kg.On January 31, 2009, the Government of Canada's final assessment concluded that exposure toORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is not harmful to human health.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.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) in significant quantities.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) appears as a clear colorless liquid.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) Flash point 18°F.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) Density 7.8 lb / gal.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) Slightly soluble in water.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) Vapors are heavier than air.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) Vapors irritate the eyes and respiratory system. May polymerize if heated or contaminated. If polymerization occurs inside a container, the container may violently rupture.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) Used to make adhesives, paints, and plastics.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is an industrial chemical that is produced in large amounts in the United States.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is a clear, colorless liquid with a sweet, fruity smell. It is very flammable and may be ignited by heat, sparks, or flames. Vinyl acetate 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 7365 HP is used to modify mixtures containing various binders. Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP provides adhesion of mortars thanks to its special physical / chemical composition. Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP increases wear resistance, elasticity and water resistance. ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) provides excellent water resistance. Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP provides elasticity. Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP thanks to its compressive strength, ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) can be used for plasters in SPTC. In addition to excellent abrasion, flexibility and water resistance, ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) can be used in tile joint filling compounds. ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) is a redispersible powder obtained by drying a Vinyl Acetate / Acrylic copolymer emulsion with PVA as a protective colloid. The chemical composition of the polymer allows the redispersible polymer to coalesce at low temperatures and provides good adhesion to Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP mineral substrates. ORP 7365 HP is used to modify mixtures containing various binders. ORP 7365 HP increases the adhesion of mortars thanks to its special physical / chemical composition, Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP abrasion resistance, Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP elasticity and Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP water resistance. Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP can be used for plasters in ORP 7365 HP SPTC thanks to its excellent water resistance, elasticity and compressive strength. ORP 7365 HP can be used in one-component waterproofing mortars thanks to the excellent flexibility, hydrophobicity and water resistance of ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer). With its excellent abrasion, flexibility and water resistance, ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) can be used in tile joint filling compounds. ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) is a redispersible powder produced by drying a Vinyl Acetate / Acrylic copolymer emulsion with PVOH as a protective colloid. The specific chemical composition of the polymer allows the re-dispersed polymer to coalesce at low temperatures and provides good adhesion to cement-based substrates. ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) is used to modify mixtures containing hydraulic binders. Due to the special chemical / physical composition of ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer), ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) increases the adhesion, abrasion resistance, flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or cement.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is also used as a coating in plastic films for food packaging and as a modifier of food starch.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is an acetate ester.At 20 °C, a saturated solution of vinyl acetate in water contains 2.0-2.4 wt % ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer), whereas a saturated solution of water in ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) contains 0.9-1.0 wt % water; at 50 °C, the solubility of ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) in water is 0.1 wt % more than at 20 °C, but the solubility of water in ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) doubles to about 2 wt %.The/ fate of inhaled ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) in rabbits /was studied.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) tended to remain in the body after ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) was inhaled; 70% of the ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) administered was retained, and an equilibrium was established in the first few min after exposure began.No ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) /was found/ in the blood, either during or after its inhalation, which suggested.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is rapidly metabolized when ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) enters the body through the lungs.The hydrolysis of ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) was studied in vitro with rat liver and lung microsomes, rat and human plasma and purified esterases (acetylcholine esterase, butyrylcholine esterase, carboxyl esterase).In order to establish the rate of metab of ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) in vivo, rats were exposed in closed desiccator jar chambers, and gas uptake kinetics were studied. The decay of ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) was dose-dependent, indicating possible satn of metabolic pathway(s). The maximal clearance (at lower concn) of ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) from the system (30,000 mL/hr/kg) was similar to the maximal ventilation rate in this species. The exposure of rats to ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) resulted in a transient exhalation of significant amts of acetaldehyde into the closed exposure system.Attempts have been undertaken to determine ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) can be concluded, that 63 % of orally applied 14C vinyl acetate is excreted as metabolites.Rats were administered oral doses of 14C-ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) (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.Two male Wistar Rats exposed to ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) (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 vinyl acetate exposure levels exceeded 650 ppm (2320 mg/cu m).ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 7365 HP (Vinyl Acetate,Acrylic Copolymer) and acetaldehyde by gas chromatography ... Acetaldehyde was found in expired air at all ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) exposure concentrations. With increasing the ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) exposure, concentration of acetaldehyde in expired air increased. At vinyl acetate exposure of approximately 1000 ppm the concentration of acetaldehyde in the expired air was 277 ppm (499 mg/cu m).Gas chromatographic analysis of human whole-blood lymphocyte cultures treated for 10 seconds to 20 min with ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) (5.4 mM) revealed a rapid degradation of ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) and formation of acetaldehyde. During the 20 min observation period, no degradation of ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) or formation of acetaldehyde were observed in complete culture medium without blood, which suggested that the reaction was enzymatic.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 7365 HP (Vinyl Acetate,Acrylic Copolymer) in the nasal cavity of the rat.To provide validation data for this model, controlled human exposures at exposure levels of 1, 5 and 10 ppm to inhaled ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 7365 HP (Vinyl Acetate,Acrylic Copolymer) and acetaldehyde were compared with data from the human nasal model simulation. For the ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) data a good fit was demonstrated (r = 0.9).Finally, solutions of ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) were placed in the mouth of anesthetized rats for 10 min and then analyzed for acetaldehyde concentrations.The metabolism of ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) has been studied in animals . ORP 7365 HP 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 substraHtes. ORP 7365 HP is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) improves adhesion, ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) improves abrasion resistance, ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) improves flexibility and ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) improves water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially in the systems that require water resistance, flexibility and abrasion resistance at the same time ORP 7365 HP provides excellent performance.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 7365 HP (Vinyl Acetate,Acrylic Copolymer) (200-2,000 ppm) in the air for 1.4 hours or less. The results show that ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) is rapidly metabolized by blood esterases and that hepatic monooxygenases have a minor role, if any, in the metabolism of ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer).In vitro metabolic studies show that ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 7365 HP (Vinyl Acetate,Acrylic Copolymer). The highest decrease (50%) in SH content was seen in guinea pigs following a single intraperitoneal injection of 500 mg/kg ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer). Glutathione conjugation may decrease the toxicity of potentially harmful electrophiles by facilitating excretion into the bile. These studies show that ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 7365 HP (Vinyl Acetate,Acrylic Copolymer) may bind to various degrees with glutathione in different species, which may help to detoxify ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) or its metabolites and enhance their elimination.ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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 7365 HP (Vinyl Acetate,Acrylic Copolymer) metabolism not only takes place in the liver but also in several tissues.Acetaldehyde is a metabolite of ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) through esterase-mediated metabolism. It is discussed that ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) exhibits its genotoxicity via acetaldehyde. For example /researchers/ demonstrated that ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) induces /DNA protein crosslinking/ via acetaldehyde, and ... chromosomal damage induced by ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) 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).ORP 7365 HP (Vinyl Acetate,Acrylic Copolymer) occurs in small quantities in human blood. Therefore, it may well be that acetaldehyde expresses its genotoxic potential in case of metabolic overload. ORP 7365 HP can be used in one-component waterproofing mortars thanks to the excellent flexibility, hydrophobicity and water resistance of ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer). With its excellent abrasion, flexibility and water resistance, ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) can be used in tile joint filling compounds. ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) is a redispersible powder produced by drying a Vinyl Acetate / Acrylic copolymer emulsion with PVOH as a protective colloid. The specific chemical composition of the polymer allows the re-dispersed polymer to coalesce at low temperatures and provides good adhesion to cement-based substrates. ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) is used to modify mixtures containing hydraulic binders. Due to the special chemical / physical composition of ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer), ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) increases the adhesion, abrasion resistance, flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or cement. Lime. While ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) systems require water resistance, flexibility and abrasion resistance, ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) provides excellent performance. With its excellent abrasion resistance, flexibility and water resistance, ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) can be used between 2.0 - 4.0% in tile mortar formulations. ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) can also be used in EIFS due to its excellent water resistance, flexibility and compressive strength. Waterproofing Mortars: ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) can be used between 7.0 - 10.0% in single component waterproofing mortars due to its excellent flexibility, hydrophobicity and water resistance. polymer powder based vinilatsetatnoho-acrylic copolymer ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) is a hydrophobic polymer powder. ORP 7365 HP is used to modify mixtures containing various binders. Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP provides adhesion of mortars thanks to its special physical / chemical composition. Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP increases wear resistance, elasticity and water resistance. ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) provides excellent water resistance. Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP provides elasticity. Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP thanks to its compressive strength, ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) can be used for plasters in SPTC. In addition to excellent abrasion, flexibility and water resistance, ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) can be used in tile joint filling compounds. ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer) is a redispersible powder obtained by drying a Vinyl Acetate / Acrylic copolymer emulsion with PVA as a protective colloid. The chemical composition of the polymer allows the redispersible polymer to coalesce at low temperatures and provides good adhesion to Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP mineral substrates. ORP 7365 HP is used to modify mixtures containing various binders. ORP 7365 HP increases the adhesion of mortars thanks to its special physical / chemical composition, Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP abrasion resistance, Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP elasticity and Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP water resistance. Vinyl Acetate, Acrylic Copolymer - ORP 7365 HP can be used for plasters in ORP 7365 HP SPTC thanks to its excellent water resistance, elasticity and compressive strength. ORP 7365 HP can be used in one-component waterproofing mortars thanks to the excellent flexibility, hydrophobicity and water resistance of ORP 7365 HP (Vinyl Acetate, Acrylic Copolymer).
ORP 7365 HP
ORP 7365 HP Hydrophobic Redispersible Powder for Dry-Mix Mortars INTRODUCTION ORP 7365 HP 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 7365 HP is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 7365 HP improves adhesion, abrasion resistance,flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially in the systems that require water resistance, flexibility and abrasion resistance at the same time ORP 7365 HP provides excellent performance. TYPICAL PROPERTIES Appearance: White powder Chemical composition: VA / Acrylic Copolymer Stabilizing System: PVOH Residual Humidity (%): Max. 1.5 Density (g/l): 400 - 600 Ash Content (%):14 ± 2 Alkali Resistance: High After 1:1 Dispersion with Water pH:8.0 – 9.0 MFFT (°C): 0 APPLICATION AREAS Tile Grouts: Having excellent abrasion resistance, flexibility and water resistance ORP 7365 HP can be used in tile grouts formulations, between 2.0 – 4.0 %. EIFS Plasters: Because of providing excellent water resistance, flexibility and compressive strength ORP 7365 HP can be used also in EIFS plaster formulations, between 3.0 – 5.0 % Water Proofing Mortars: ORP 7365 HP can be used in one component water proofing mortars, between 7.0 – 10.0% because of having excellent flexibility, hydrophobicity and water resistance. PRODUCT HANDLING – STORAGE – SHELFLIFE Packaging: Pallet with 18 or 30 paper bags, each 25 kg (450 or 750 kg) also 500 kg of big bags. Packages must be stored in a dry and cool warehouse at temperatures between 10 – 25 °C. 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 7365 HP has to be used within 12 months.
ORP 7365 HP
ORP 7365 HP ORP 7365 HP 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 7365 HP is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 7365 HP improves adhesion, abrasion resistance,flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially in the systems that require water resistance, flexibility and abrasion resistance at the same time ORP 7365 HP provides excellent performance. TYPICAL PROPERTIES Appearance White powder Chemical composition VA / Acrylic Copolymer Stabilizing System PVOH Residual Humidity (%) Max. 1.5 Density (g/l) 400 - 600 Ash Content (%) 14 ± 2 Alkali Resistance High After 1:1 Dispersion with Water pH 8.0 – 9.0 MFFT (°C) 0 APPLICATION AREAS Tile Grouts: Having excellent abrasion resistance, flexibility and water resistance ORP 7365 HP can be used in tile grouts formulations, between 2.0 – 4.0 %. EIFS Plasters: Because of providing excellent water resistance, flexibility and compressive strength ORP 7365 HP can be used also in EIFS plaster formulations, between 3.0 – 5.0 % Water Proofing Mortars: ORP 7365 HP can be used in one component water proofing mortars, between 7.0 – 10.0% because of having excellent flexibility, hydrophobicity and water resistance. PRODUCT HANDLING – STORAGE – SHELFLIFE Packaging: Pallet with 18 or 30 paper bags, each 25 kg (450 or 750 kg) also 500 kg of big bags. Packages must be stored in a dry and cool warehouse at temperatures between 10 – 25 °C. 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 12 months. ORP 7365 HP 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 7365 HP is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 7365 HP improves adhesion, flexibility and water resistance of mortars containing hydraulic binders such as cement, gypsum or lime. Especially in self levelling mortar formulations ORP 7365 HP provides excellent abrasion resistance, flexural & compressive stength and good leveling. APPLICATION AREAS of ORP 7365 HP ORP 7365 HP 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 7365 HP 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 7365 HP has to be used within 6 months after the date of delivery. ORP 7365 HP is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 7365 HP 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 7365 HP performs very well in transverse deformation conditions. APPLICATION AREAS of ORP 7365 HP ORP 7365 HP 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 7365 HP can be used with the ratio of 2.0 - 4.0 % in weight and without requiring an additional hydrophobic agent. Moreover ORP 7365 HP 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 7365 HP performs very well in cementitious exterior plasters and topcoats with the amunt of 2.0 - 4.0 %. PRODUCT HANDLING - STORAGE - SHELFLIFE of ORP 7365 HP 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 7365 HP 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 7365 HP in water contains 2.0-2.4 wt % ORP 7365 HP , whereas a saturated solution of water in ORP 7365 HP contains 0.9-1.0 wt % water; at 50 °C, the solubility of ORP 7365 HP in water is 0.1 wt % more than at 20 °C, but the solubility of water in ORP 7365 HP doubles to about 2 wt % The/ fate of inhaled ORP 7365 HP in rabbits /was studied/. ... ORP 7365 HP tended to remain in the body after it was inhaled; 70% of the ORP 7365 HP administered was retained, and an equilibrium was established in the first few min after exposure began. ... No ORP 7365 HP /was found/ in the blood, either during or after its inhalation, which suggested ... that ORP 7365 HP is rapidly metabolized when it enters the body through the lungs. Two male Wistar Rats exposed to ORP 7365 HP (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 7365 HP exposure levels exceeded 650 ppm (2320 mg/cu m). ORP 7365 HP 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 7365 HP 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 7365 HP and acetaldehyde by gas chromatography ... Acetaldehyde was found in expired air at all ORP 7365 HP exposure concentrations. With increasing the ORP 7365 HP exposure, concentration of acetaldehyde in expired air increased. At ORP 7365 HP 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 7365 HP (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 7365 HP 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 7365 HP 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 7365 HP is excreted as metabolites. ORP 7365 HP is an organic compound with the formula CH3CO2CH=CH2. This colorless liquid is the precursor to polyORP 7365 HP , an important industrial polymer. 1 Production of ORP 7365 HP 2 Preparation of ORP 7365 HP 2.1 Mechanism of ORP 7365 HP 2.2 Alternative routes 3 Polymerization of ORP 7365 HP 4 Other reactions of ORP 7365 HP 5 Toxicity evaluation of ORP 7365 HP Production of ORP 7365 HP The worldwide production capacity of ORP 7365 HP 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 7365 HP is the acetate ester of vinyl alcohol. Since vinyl alcohol is highly unstable (with respect to acetaldehyde), the preparation of ORP 7365 HP 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 7365 HP and a palladium hydride, which would be oxidized to give hydroxide. Polymerization It can be polymerized to give polyORP 7365 HP (PVA). With other monomers it can be used to prepare various copolymers such as ethylene-ORP 7365 HP (EVA), ORP 7365 HP -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 7365 HP 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 7365 HP undergoes transesterification, giving access to vinyl ethers: ROH + CH2=CHOAc → ROCH=CH2 + HOAc Toxicity evaluation Tests suggest that ORP 7365 HP 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 7365 HP 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. On/ hydrolysis /in the blood/, ORP 7365 HP 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 7365 HP 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 7365 HP in vivo, rats were exposed in closed desiccator jar chambers, and gas uptake kinetics were studied. The decay of ORP 7365 HP was dose-dependent, indicating possible satn of metabolic pathway(s). The maximal clearance (at lower concn) of ORP 7365 HP from the system (30,000 mL/hr/kg) was similar to the maximal ventilation rate in this species. The exposure of rats to ORP 7365 HP resulted in a transient exhalation of significant amts of acetaldehyde into the closed exposure system. 1.1. Product identifier Product name ORP 7365 HP 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 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. Gas chromatographic analysis of human whole-blood lymphocyte cultures treated for 10 seconds to 20 min with ORP 7365 HP (5.4 mM) revealed a rapid degradation of ORP 7365 HP and formation of acetaldehyde. During the 20 min observation period, no degradation of ORP 7365 HP or formation of acetaldehyde were observed in complete culture medium without blood, which suggested that the reaction was enzymatic. ORP 7365 HP 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 7365 HP 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 7365 HP 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 7365 HP and acetaldehyde were compared with data from the human nasal model simulation. For the ORP 7365 HP data a good fit was demonstrated (r = 0.9). The metabolism of ORP 7365 HP has been studied in animals ... ORP 7365 HP 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 7365 HP 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 7365 HP (200-2,000 ppm) in the air for 1.4 hours or less. The results show that ORP 7365 HP is rapidly metabolized by blood esterases and that hepatic monooxygenases have a minor role, if any, in the metabolism of ORP 7365 HP. In vitro metabolic studies show that ORP 7365 HP 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 7365 HP 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 7365 HP . The highest decrease (50%) in SH content was seen in guinea pigs following a single intraperitoneal injection of 500 mg/kg ORP 7365 HP . Glutathione conjugation may decrease the toxicity of potentially harmful electrophiles by facilitating excretion into the bile. These studies show that ORP 7365 HP 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 7365 HP 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 7365 HP may bind to various degrees with glutathione in different species, which may help to detoxify ORP 7365 HP or its metabolites and enhance their elimination. ORP 7365 HP 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 7365 HP metabolism not only takes place in the liver but also in several tissues. The half-life of /200 uM/ ORP 7365 HP 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 7365 HP through esterase-mediated metabolism. It is discussed that ORP 7365 HP exhibits its genotoxicity via acetaldehyde. For example /researchers/ demonstrated that ORP 7365 HP induces /DNA protein crosslinking/ via acetaldehyde, and ... chromosomal damage induced by ORP 7365 HP 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 7365 HP is primarily used as a monomer in the production of polyORP 7365 HP and polyvinyl alcohol. Its chief use is as a monomer for making poly(ORP 7365 HP ) and ORP 7365 HP 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 7365 HP 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 7365 HP has been used primarily to produce polyORP 7365 HP emulsions and polyvinyl alcohol. The principle use of these emulsions has been in adhesives, paints, textiles, and paper products. PRODUCT PROFILE: ORP 7365 HP : PolyORP 7365 HP accounts for about 48% of ORP 7365 HP 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 7365 HP (EVA) polymers, ethylene vinyl alcohol (EVOH) barrier resins. PRODUCT PROFILE: ORP 7365 HP : ORP 7365 HP monomer's (VAM) main use is polyORP 7365 HP 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 7365 HP (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 7365 HP : ORP 7365 HP monomer (VAM) is mainly used in polyORP 7365 HP 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 7365 HP (EVA) polymers, ethylene vinyl alcohol (EVOH) barrier resins and polyvinyl butyral (PVB). CHEMICAL PROFILE: ORP 7365 HP . PolyORP 7365 HP emulsions and resins, 40%; (this area is divided evenly between paints and adhesives); polyvinyl alcohol, 15%; polyvinyl butyral, 8%; ethylene-ORP 7365 HP resins, 6%; polyvinyl chloride copolymers, 3%; miscellaneous, 1%; exports, 27%. CHEMICAL PROFILE: ORP 7365 HP : PolyORP 7365 HP emulsions and resins, 57%; polyvinyl alcohol, 19%; polyvinyl butyral, 10%; ethylene-ORP 7365 HP resins, 8%; ethylene vinyl alcohol, 2%; miscellaneous, including polyvinyl chloride copolymers, 4%. PRODUCT FOCUS: ORP 7365 HP Monomer (VAM): Global Demand: 2003: 4.3 million tonnes. PolyORP 7365 HP , 44%; polyORP 7365 HP , 40%; ethylene vinyl alcohol, 12%. ORP 7365 HP , acetic anhydride, ethanol, methanol, and formaldehyde were formed in aq extracts of polyORP 7365 HP films only in some cases and in insignificant quantities. The difference between pH of aq extracts of polyORP 7365 HP 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 7365 HP film extracts and up to 12.3 mg bromide/L in inactivated extracts. The oxidizability of the polyORP 7365 HP 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 7365 HP . 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 7365 HP 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 7365 HP has satisfactory properties for medicinal use. ORP 7365 HP 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 7365 HP 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 7365 HP is also used as a coating in plastic films for food packaging and as a modifier of food starch. ORP 7365 HP is primarily used as a monomer in the production of polyORP 7365 HP and polyvinyl alcohol. Acute (short-term) inhalation exposure of workers to ORP 7365 HP 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 7365 HP 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 7365 HP for carcinogenicity. ORP 7365 HP 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 7365 HP (427 °C) shall be used in ORP 7365 HP storage areas. The storage of ORP 7365 HP in glass containers should not be in the same areas as oxidizing agents or other incompatible chemicals. Containers of ORP 7365 HP 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 7365 HP . There is limited evidence in experimental animals for the carcinogenicity of ORP 7365 HP . Overall evaluation: ORP 7365 HP is possibly carcinogenic to humans (Group 2B). In making the overall evaluation, the working group took into account the following evidence: (1) ORP 7365 HP 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 7365 HP and acetaldehyde induce nasal cancer in rats after administration by inhalation. (3) ORP 7365 HP 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 7365 HP 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 7365 HP 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 7365 HP in both tissue types. Semicarbazide, an aldehyde scavenger, was unable to protect the tissues from ORP 7365 HP -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 7365 HP 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 7365 HP during resting and light exercise at three exposure levels (1, 5 and 10 ppm nominally). Both, labeled ORP 7365 HP 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 0.8 sec in an exposure period of 2 to 5 min resulting in data during all phases of the breathing. The rate of sampling was rapid enough to capture much of the behavior of ORP 7365 HP in the human nasal cavity including inhalation and exhalation. However, the sampling was not frequent enough to accurately capture the peak concentration in every breath. ORP 7365 HP 's production and use as a monomer for making poly (ORP 7365 HP) and ORP 7365 HP copolymers, in the production of paints, sealants, coatings, and binders and in miscellaneous uses such as chewing gum and tablet coatings may result in its release to the environment through various waste streams. If released to air, a vapor pressure of 90.2 mm Hg at 20 °C indicates ORP 7365 HP will exist solely as a vapor in the ambient atmosphere. Vapor-phase ORP 7365 HP is expected to be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 14 hours. If released to soil, ORP 7365 HP is expected to have high mobility based upon an estimated Koc of 60. Although leaching is possible, concurrent hydrolysis will decrease its importance. Volatilization from moist soil surfaces is also expected to be an important fate process based upon an estimated Henry's Law constant of 5.1X10-4 atm-cu m/mole. ORP 7365 HP may volatilize from dry soil surfaces based upon its vapor pressure. Polymerization may occur in sunlight. Biodegradation of ORP 7365 HP may be an important environmental fate process in soil under both aerobic (51 to 62% biodegradation reached in 5 day BOD test using sewage inoculum) and anaerobic conditions (nearly complete degradation in 26 hrs); reaction products of acetaldehyde and acetate are formed under both oxygen conditions. If released to water, ORP 7365 HP is not expected to adsorb to suspended solids and sediment in water based on the estimated Koc value. Volatilization from water surfaces is expected to be an important fate process based on its estimated Henry's Law constant. Estimated volatilization half-lives for a model river and model lake are 4 hours and 4 days, respectively. A 98% of theoretical BOD was reported using activated sludge in the Japanese MITI test, suggesting that biodegradation may be an important environmental fate process in water. An estimated BCF of 3.2 suggests the potential for bioconcentration in aquatic organisms is low. Degradation by hydrolysis (half-life of 7.3 days at 25 °C and pH 7) and by photochemically produced oxidants will occur. Occupational exposure to ORP 7365 HP may occur through inhalation and dermal contact with this compound at workplaces where ORP 7365 HP is produced or used. The general population may be exposed to ORP 7365 HP through inhalation and dermal contact with products containing ORP 7365 HP ; limited exposure may occur via ingestion from its use in chewing gum and tablet coatings. (SRC) ORP 7365 HP 's production and use as a monomer for making poly(ORP 7365 HP ) and ORP 7365 HP copolymers, in the production of paints, films, sealants, lacquers, coatings, food packaging, and binders, in chewing gum and as a tablet coating(1,2) and safety glass(3) may result in its release to the environment through various
ORP 7680
Product name ORP 7680 SL Chemical name and synonym VA / Acrylic copolymer ORP 7680 TYPICAL PROPERTIES ORP 7680 Appearance White powder ORP 7680 Chemical composition VA / Acrylic Copolymer ORP 7680 Stabilizing System PVOH ORP 7680 Residual Humidity (%) Max. 2.0 ORP 7680 Bulk Density (g/l) 400 - 600 ORP 7680 Ash Content (%) 12 ± 2 ORP 7680 Alkali Resistance High ORP 7680 After 1:1 Dispersion with Water MFFT (°C) 5 ± 1 ORP 7680 Information on basic physical and chemical properties. ORP 7680 Appearance powder ORP 7680 Colour white ORP 7680 Odour characteristic ORP 7680 Odour threshold. Not available. ORP 7680 pH. 5,0-8,0 (1:1 aqueous soln.) ORP 7680 Melting point / freezing point. Not available. ORP 7680 Initial boiling point. Not applicable. ORP 7680 Boiling range. Not available. ORP 7680 Flash point. Not applicable. ORP 7680 Evaporation Rate Not available. ORP 7680 Flammability of solids and gases Not available. ORP 7680 Lower inflammability limit. 20 g/m3. ORP 7680 Upper inflammability limit. Not available. ORP 7680 Lower explosive limit. Not available. ORP 7680 Upper explosive limit. Not available. ORP 7680 Vapour pressure. Not available. ORP 7680 Vapour density Not available. ORP 7680 Relative density. Not available. ORP 7680 Solubility Not available. ORP 7680 Partition coefficient: n-octanol/water Not available. ORP 7680 Auto-ignition temperature. 300 °C. > ORP 7680 Decomposition temperature. Not available. ORP 7680 Viscosity Not available. ORP 7680 Explosive properties Not available. ORP 7680 Oxidising properties Not available. ORP 7680 Other information. ORP 7680 Bulk density 400 - 600 g/l ORP 7680 Min. Cloud Ignition temperature ca. 480°C ORP 7680 Dust explosion class 1 ORP 7680 Kst value 122 bar.m/sec ORP 7680 Maximum explosion pressure 6,7 bar ORP 7680 Minimum ignition energy 3 - 10 mJ with inductance ORP 7680 Glow temperature >400°C ORP 7680 SL-Redispersible Powder for Self Leveling Dry-Mix Mortars.ORP 7680 SL 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 7680 SL is used to modify mixtures containing hydraulic binders. Due to its particular chemical / 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 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.ORP 7680 SL is a redispersible powder obtained by drying a Vinyl Acetate / Acrylic Copolymer emulsion with PVA as a protective colloid. The specific chemical composition of the polymer ensures the coalescence of the redispersible polymer at low temperatures and ensures good adhesion to various substrates.ORP 7680 SL is used for modifying mixtures containing various binders. Due to its special physical / chemical composition, ORP 7680 SL improves the adhesion, flexibility and water resistance of mortars containing cement, gypsum or lime. Especially in self-leveling mortar formulations, ORP 7680 SL provides excellent abrasion resistance, high flexural and compressive strength, and good leveling during application. ORP 7680 EYES: Remove contact lenses, if present. Wash immediately with plenty of water for at least 15 minutes, opening the eyelids fully. If problem persists, seek medical advice. ORP 7680 SKIN: Remove contaminated clothing. Wash immediately with plenty of water. If irritation persists, get medical advice/attention. Wash contaminated clothing before using it again. ORP 7680 INHALATION: Remove to open air. In the event of breathing difficulties, get medical advice/attention immediately. ORP 7680 INGESTION: Get medical advice/attention. Induce vomiting only if indicated by the doctor. Never give anything by mouth to an unconscious person, unless authorised by a doctor. ORP 7680 Extinguishing media. SUITABLE EXTINGUISHING EQUIPMENT The extinguishing equipment should be of the conventional kind: carbon dioxide, foam, powder and water spray. UNSUITABLE EXTINGUISHING EQUIPMENT None in particular. ORP 7680 Special hazards arising from the substance or mixture. HAZARDS CAUSED BY EXPOSURE IN THE EVENT OF FIRE Do not breathe combustion products. The product is combustible and, when the powder is released into the air in sufficient concentrations and in the presence of a source of ignition, it can create explosive mixtures with air. Fires may start or get worse by leakage of the solid product from the container, when it reaches high temperatures or through contact with sources of ignition. ORP 7680 Advice for firefighters. GENERAL INFORMATION Use jets of water to cool the containers to prevent product decomposition and the development of substances potentially hazardous for health. Always wear full fire prevention gear. Collect extinguishing water to prevent it from draining into the sewer system. Dispose of contaminated water used for extinction and the remains of the fire according to applicable regulations. SPECIAL PROTECTIVE EQUIPMENT FOR FIRE-FIGHTERS Normal fire fighting clothing i.e. fire kit (BS EN 469), gloves (BS EN 659) and boots (HO specification A29 and A30) in combination with self-contained open circuit positive pressure compressed air breathing apparatus (BS EN 137). ORP 7680 Personal precautions, protective equipment and emergency procedures. Use breathing equipment if fumes or powders are released into the air. These indications apply for both processing staff and those involved in emergency procedures. Avoid dust formation. Do not breathe dust. ORP 7680 Environmental precautions. The product must not penetrate into the sewer system or come into contact with surface water or ground water. Cover any spilled material in accordance with regulations to prevent dispersal by wind. ORP 7680 Methods and material for containment and cleaning up. Confine using earth or inert material. Collect as much material as possible and eliminate the rest using jets of water. Contaminated material should be disposed of in compliance with the provisions set forth in point 13. ORP 7680 Reference to other sections. Any information on personal protection and disposal is given in sections 8 and 13. Eliminate all source of ignition. Observe notes under section 7. ORP 7680 Precautions for safe handling. Before handling the product, consult all the other sections of this material safety data sheet. Avoid leakage of the product into the environment. Do not eat, drink or smoke during use. Avoid dust formation. Increased risk of slipping if substance comes into contact with water. ORP 7680 Conditions for safe storage, including any incompatibilities. Keep the product in clearly labelled containers. Keep containers away from any incompatible materials, see section 10 for details. The bags have to be stored in a closed, cool, and dry place. The bags have to be protected from high humudity and high temperatures above 25°C (77°F). Dusting has to be avoided, since it may create explosive mixture with air. Take precautionary measures against electrostatic charging. Keep away from open flames, heat and sparks. ORP 7680 Exposure controls. Comply with the safety measures usually applied when handling chemical substances. ORP 7680 HAND PROTECTION In the case of prolonged contact with the product, protect the hands with penetration-resistant work gloves (see standard EN 374). Work glove material must be chosen according to the use process and the products that may form. Latex gloves may cause sensitivity reactions. ORP 7680 SKIN PROTECTION None required. ORP 7680 EYE PROTECTION Wear airtight protective goggles (see standard EN 166). ORP 7680 RESPIRATORY PROTECTION Use a type P filtering facemask (see standard EN 149) or equivalent device, whose class (1, 2 or 3) and effective need, must be defined according to the outcome of risk assessment. ORP 7680 ENVIRONMENTAL EXPOSURE CONTROLS. The emissions generated by manufacturing processes, including those generated by ventilation equipment, should be checked to ensure compliance with environmental standards. ORP 7680 Reactivity. There are no particular risks of reaction with other substances in normal conditions of use. ORP 7680 Chemical stability.The product is stable in normal conditions of use and storage. ORP 7680 Possibility of hazardous reactions.No hazardous reactions are foreseeable in normal conditions of use and storage. ORP 7680 Conditions to avoid. None in particular. However the usual precautions used for chemical products should be respected. ORP 7680 Incompatible materials. Information not available. ORP 7680 Hazardous decomposition products. Information not available.
ORP 7680 SL
ORP 7680 SL ORP 7680 SL 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 7680 SL is used to modify mixtures containing hydraulic binders. Due to its particular chemical / 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. APPLICATION AREAS of ORP 7680 SL 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 – SHELFLIFE of ORP 7680 SL 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. ORP 7680 SL is used to modify mixtures containing hydraulic binders. Due to its particular chemical / physical composition, ORP 7680 SL 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 7680 SL performs very well in transverse deformation conditions. TYPICAL PROPERTIES of ORP 7680 SL 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 7680 SL ORP 7680 SL 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 7680 SL can be used with the ratio of 2.0 - 4.0 % in weight and without requiring an additional hydrophobic agent. Moreover ORP 7680 SL 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 7680 SL performs very well in cementitious exterior plasters and topcoats with the amunt of 2.0 - 4.0 %. PRODUCT HANDLING - STORAGE - SHELFLIFE of ORP 7680 SL 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 7680 SL 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 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 7680 SL is an organic compound with the formula CH3CO2CH=CH2. This colorless liquid is the precursor to polyORP 7680 SL , an important industrial polymer.[3] 1 Production of ORP 7680 SL 2 Preparation of ORP 7680 SL 2.1 Mechanism of ORP 7680 SL 2.2 Alternative routes 3 Polymerization of ORP 7680 SL 4 Other reactions of ORP 7680 SL 5 Toxicity evaluation of ORP 7680 SL 6 See also 7 References 8 External links Production of ORP 7680 SL The worldwide production capacity of ORP 7680 SL 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 7680 SL is the acetate ester of vinyl alcohol. Since vinyl alcohol is highly unstable (with respect to acetaldehyde), the preparation of ORP 7680 SL 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 7680 SL and a palladium hydride, which would be oxidized to give hydroxide. Polymerization It can be polymerized to give polyORP 7680 SL (PVA). With other monomers it can be used to prepare various copolymers such as ethylene-ORP 7680 SL (EVA), ORP 7680 SL -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 7680 SL 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 7680 SL undergoes transesterification, giving access to vinyl ethers:[10][11] ROH + CH2=CHOAc → ROCH=CH2 + HOAc Toxicity evaluation Tests suggest that ORP 7680 SL 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 7680 SL 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 7680 SL 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 7680 SL in water contains 2.0-2.4 wt % ORP 7680 SL , whereas a saturated solution of water in ORP 7680 SL contains 0.9-1.0 wt % water; at 50 °C, the solubility of ORP 7680 SL in water is 0.1 wt % more than at 20 °C, but the solubility of water in ORP 7680 SL doubles to about 2 wt % The/ fate of inhaled ORP 7680 SL in rabbits /was studied/. ... ORP 7680 SL tended to remain in the body after it was inhaled; 70% of the ORP 7680 SL administered was retained, and an equilibrium was established in the first few min after exposure began. ... No ORP 7680 SL /was found/ in the blood, either during or after its inhalation, which suggested ... that ORP 7680 SL is rapidly metabolized when it enters the body through the lungs. Two male Wistar Rats exposed to ORP 7680 SL (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 7680 SL exposure levels exceeded 650 ppm (2320 mg/cu m). ORP 7680 SL 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 7680 SL 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 7680 SL and acetaldehyde by gas chromatography ... Acetaldehyde was found in expired air at all ORP 7680 SL exposure concentrations. With increasing the ORP 7680 SL exposure, concentration of acetaldehyde in expired air increased. At ORP 7680 SL 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 7680 SL (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 7680 SL 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 7680 SL 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 7680 SL is excreted as metabolites. On/ hydrolysis /in the blood/, ORP 7680 SL 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 7680 SL 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 7680 SL in vivo, rats were exposed in closed desiccator jar chambers, and gas uptake kinetics were studied. The decay of ORP 7680 SL was dose-dependent, indicating possible satn of metabolic pathway(s). The maximal clearance (at lower concn) of ORP 7680 SL from the system (30,000 mL/hr/kg) was similar to the maximal ventilation rate in this species. The exposure of rats to ORP 7680 SL 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 7680 SL (5.4 mM) revealed a rapid degradation of ORP 7680 SL and formation of acetaldehyde. During the 20 min observation period, no degradation of ORP 7680 SL or formation of acetaldehyde were observed in complete culture medium without blood, which suggested that the reaction was enzymatic. ORP 7680 SL 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 7680 SL 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 7680 SL 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 7680 SL and acetaldehyde were compared with data from the human nasal model simulation. For the ORP 7680 SL data a good fit was demonstrated (r = 0.9). The metabolism of ORP 7680 SL has been studied in animals ... ORP 7680 SL 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 7680 SL 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 7680 SL (200-2,000 ppm) in the air for 1.4 hours or less. The results show that ORP 7680 SL is rapidly metabolized by blood esterases and that hepatic monooxygenases have a minor role, if any, in the metabolism of ORP 7680 SL . In vitro metabolic studies show that ORP 7680 SL 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 7680 SL 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 7680 SL . The highest decrease (50%) in SH content was seen in guinea pigs following a single intraperitoneal injection of 500 mg/kg ORP 7680 SL . Glutathione conjugation may decrease the toxicity of potentially harmful electrophiles by facilitating excretion into the bile. These studies show that ORP 7680 SL 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 7680 SL 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 7680 SL may bind to various degrees with glutathione in different species, which may help to detoxify ORP 7680 SL or its metabolites and enhance their elimination. ORP 7680 SL 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 7680 SL metabolism not only takes place in the liver but also in several tissues. The half-life of /200 uM/ ORP 7680 SL 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 7680 SL through esterase-mediated metabolism. It is discussed that ORP 7680 SL exhibits its genotoxicity via acetaldehyde. For example /researchers/ demonstrated that ORP 7680 SL induces /DNA protein crosslinking/ via acetaldehyde, and ... chromosomal damage induced by ORP 7680 SL 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 7680 SL is primarily used as a monomer in the production of polyORP 7680 SL and polyvinyl alcohol. Its chief use is as a monomer for making poly(ORP 7680 SL ) and ORP 7680 SL 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 7680 SL 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 7680 SL has been used primarily to produce polyORP 7680 SL emulsions and polyvinyl alcohol. The principle use of these emulsions has been in adhesives, paints, textiles, and paper products. PRODUCT PROFILE: ORP 7680 SL : PolyORP 7680 SL accounts for about 48% of ORP 7680 SL 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 7680 SL (EVA) polymers, ethylene vinyl alcohol (EVOH) barrier resins. PRODUCT PROFILE: ORP 7680 SL : ORP 7680 SL monomer's (VAM) main use is polyORP 7680 SL 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 7680 SL (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 7680 SL : ORP 7680 SL monomer (VAM) is mainly used in polyORP 7680 SL 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 7680 SL (EVA) polymers, ethylene vinyl alcohol (EVOH) barrier resins and polyvinyl butyral (PVB). CHEMICAL PROFILE: ORP 7680 SL . PolyORP 7680 SL emulsions and resins, 40%; (this area is divided evenly between paints and adhesives); polyvinyl alcohol, 15%; polyvinyl butyral, 8%; ethylene-ORP 7680 SL resins, 6%; polyvinyl chloride copolymers, 3%; miscellaneous, 1%; exports, 27%. CHEMICAL PROFILE: ORP 7680 SL : PolyORP 7680 SL emulsions and resins, 57%; polyvinyl alcohol, 19%; polyvinyl butyral, 10%; ethylene-ORP 7680 SL resins, 8%; ethylene vinyl alcohol, 2%; miscellaneous, including polyvinyl chloride copolymers, 4%. PRODUCT FOCUS: ORP 7680 SL Monomer (VAM): Global Demand: 2003: 4.3 million tonnes. PolyORP 7680 SL , 44%; polyORP 7680 SL , 40%; ethylene vinyl alcohol, 12%. PRODUCT FOCUS: ORP 7680 SL Monomer (VAM): Global Demand: 2006: 4.8 million tonnes. PolyORP 7680 SL , 43%; polyORP 7680 SL , 42%; ethylene-ORP 7680 SL copolymers, 9%; Other, 6%. ORP 7680 SL , acetic anhydride, ethanol, methanol, and formaldehyde were formed in aq extracts of polyORP 7680 SL films only in some cases and in insignificant quantities. The difference between pH of aq extracts of polyORP 7680 SL 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 7680 SL film extracts and up to 12.3 mg bromide/L in inactivated extracts. The oxidizability of the polyORP 7680 SL 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 7680 SL . 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 7680 SL 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 7680 SL has satisfactory properties for medicinal use. ORP 7680 SL 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 7680 SL 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 7680 SL is also used as a coating in plastic films for food packaging and as a modifier of food starch. ORP 7680 SL is primarily used as a monomer in the production of polyORP 7680 SL and polyvinyl alcohol. Acute (short-term) inhalation exposure of workers to ORP 7680 SL 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 7680 SL 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 7680 SL for carcinogenicity. ORP 7680 SL 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 7680 SL (427 °C) shall be used in ORP 7680 SL storage areas. The storage of ORP 7680 SL in glass containers should not be in the same areas as oxidizing agents or other incompatible chemicals. Containers of ORP 7680 SL 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 7680 SL . There is limited evidence in experimental animals for the carcinogenicity of ORP 7680 SL . Overall evaluation: ORP 7680 SL is possibly carcinogenic to humans (Group 2B). In making the overall evaluation, the working group took into account the following evidence: (1) ORP 7680 SL 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 7680 SL and acetaldehyde induce nasal cancer in rats after administration by inhalation. (3) ORP 7680 SL 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 7680 SL 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 7680 SL 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 7680 SL in both tissue types. Semicarbazide, an aldehyde scavenger, was unable to protect the tissues from ORP 7680 SL -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 7680 SL 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 7680 SL during resting and light exercise at three exposure levels (1, 5 and 10 ppm nominally). Both, labeled ORP 7680 SL 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 0.8 sec in an exposure period of 2 to 5 min resulting in data during all phases of the breathing. The rate of sampling was rapid enough to capture much of the behavior of ORP 7680 SL in the human nasal cavity including inhalation and exhalation. However, the sampling was not frequent enough to accurately capture the peak concentration in every breath. ORP 7680 SL 's production and use as a monomer for making poly (ORP 7680 SL) and ORP 7680 SL copolymers, in the production of paints, sealants, coatings, and binders and in miscellaneous uses such as chewing gum and tablet coatings may result in its release to the environment through various waste streams. If released to air, a vapor pressure of 90.2 mm Hg at 20 °C indicates ORP 7680 SL will exist solely as a vapor in the ambient atmosphere. Vapor-phase ORP 7680 SL is expected to be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 14 hours. If released to soil, ORP 7680 SL is expected to have high mobility based upon an estimated Koc of 60. Although leaching is possible, concurrent hydrolysis will decrease its importance. Volatilization from moist soil surfaces is also expected to be an important fate process based upon an estimated Henry's Law constant of 5.1X10-4 atm-cu m/mole. ORP 7680 SL may volatilize from dry soil surfaces based upon its vapor pressure. Polymerization may occur in sunlight. Biodegradation of ORP 7680 SL may be an important environmental fate process in soil under both aerobic (51 to 62% biodegradation reached in 5 day BOD test using sewage inoculum) and anaerobic conditions (nearly complete degradation in 26 hrs); reaction products of acetaldehyde and acetate are formed under both oxygen conditions. If released to water, ORP 7680 SL is not expected to adsorb to suspended solids and sediment in water based on the estimated Koc value. Volatilization from water surfaces is expected to be an important fate process based on its estimated Henry's Law constant. Estimated volatilization half-lives for a model river and model lake are 4 hours and 4 days, respectively. A 98% of theoretical BOD was reported using activated sludge in the Japanese MITI test, suggesting that biodegradation may be an important environmental fate process in water. An estimated BCF of 3.2 suggests the potential for bioconcentration in aquatic organisms is low. Degradation by hydrolysis (half-life of 7.3 days at 25 °C and pH 7) and by photochemically produced oxidants will occur. Occupational exposure to ORP 7680 SL may occur through inhalation and dermal contact with this compound at workplaces where ORP 7680 SL is produced or used. The general population may be exposed to ORP 7680 SL through inhalation and dermal contact with products containing ORP 7680 SL ; limited exposure may occur via ingestion from its use in chewing gum and tablet coatings. (SRC) ORP 7680 SL 's production and use as a monomer for making poly(ORP 7680 SL ) and ORP 7680 SL copolymers, in the production of paints, films, sealants, lacquers, coatings, food packaging, and binders, in chewing gum and as a tablet coating(1,2) and safety glass(3) may result in its release to the environment through various waste streams(SRC). ORP 7680 SL can be released to the environment from industrial sources and biomass combustion(4). Waste gases from scrubbers (generated during the industrial manufacture of ORP 7680 SL ) may contain trace levels of ORP 7680 SL (5). TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 60(SRC), determined from a log Kow of 0.73(2) and a regression-derived equation(3), indicates that ORP 7680 SL is expected to have high mobility in soil(SRC). Volatilization of ORP 7680 SL from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 5.1X10-4 atm-cu m/mole(SRC), derived from its vapor pressure, 90.2 mm Hg(4), and water solubility, 20,000 mg/L(5). However, a hydrolysis half-life of 7.3 days (25 °C and pH 7)(6) indicates that hydrolysis may occur in moist soils and is expected to attenuate leaching in the soil column(SRC). ORP 7680 SL is expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(4). ORP 7680 SL readily polymerizes; therefore, if ORP 7680 SL is released to the environment, polymerization may occur(SRC). Complete biodegradation of ORP 7680 SL occurred using a soil inoculum within 26 hours under both anaerobic and aerobic conditions; acetaldehyde and acetate were formed as reaction products under both oxygen conditions(7). This suggests that biodegradation may be an important environmental fate process in soil(SRC). The aqueous hydrolysis half-life of ORP 7680 SL at 25 °C and pH 7 has been reported to be 7.3 days(1); the hydrolysis r
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 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 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 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
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 (Phenat)
cas no 643-79-8 o-Phthalaldehyde; o-Phthalic dicarboxaldehyde; Benzene-1,2-dicarboxaldehyde; OPA;
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.
Orthophénylphénol
cas no 7664-38-2 Phosphoric acid; Hydrogen phosphate; o-Phosphoric acid; Acide Phosphorique (French); Acido Fosforico (Italian); Fosforzuuroplossingen (Dutch); Ortho-phosphoramide; Phosphorsaeureloesungen (German); White Phosphoric Acid; Orthophosphorsäure (German);
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
Orthosiphon stamineus
clerodendranthus spicatus leaf extract; extract of the leaves of the jawa tea, orthosiphon stamineus, labiatae; kumis kuching leaf extract; orthosiphon leaf extract; java tea leaf extract CAS NO:84012-29-3
O-TOLYL BIGUANIDE
oxalic acid ethanedioic acid Aktisal Aquisal oxalate Oxiric acid Oxalsaeure Oxaalzuur Kyselina stavelova Acide oxalique Acido ossalico Acidum oxalicum CAS:144-62-7
Oud Yağı
OUD OIL ; oudh oil; AGARWOOD OIL; aetoxylon sympetalum; aetoxylon sympetalum wood oil; gaharu buaya oil; agarwood oil (aetoxylon sympetalum) CAS NO:1333524-00-7
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).
OXIDIZED POLYETHYLENE
cas no 70693-62-8 Potassium peroxymonosulfate; Potassium Peroxomonosulfate; Potassium monopersulfate triple salt; PotassiumPeroxomonosulfate; Potassium monoperoxysulfate OXONE(R);
Oxo Alcohol C 11 EO/PO
MARLOX OP 1 CAS-No.: 68937-66-6
OXO ALKOL C11 6EO/4PO
Köpüğün az olması istenilen durumlarda her tür deterjanda kullanılan temizleme özelliği olan noniyonik aktif madde
Oxo Alkol C12-15 7EO
LAURETH-4; Dehydol LS 2; Penetrant JFC; Syntanol ES 3; Synperonic L 7; Syntanol ALM 8; Tergitol 24L50; Tergitol 24L92; Surfonic L 24-2; Surfonic L 24-3; Surfonic L 24-7 CAS NO:68439-50-9
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
OXOTHIAZOLIDINE
BENZOPHENONE-3, N° CAS : 131-57-7 - Oxybenzone. Nom INCI : BENZOPHENONE-3. Nom chimique : 2-Hydroxy-4-methoxybenzophenone. N° EINECS/ELINCS : 205-031-5. Absorbant UV : Protège le produit cosmétique contre les effets de la lumière UV. Filtre UV : Permet de filtrer certains rayons UV afin de protéger la peau ou les cheveux des effets nocifs de ces rayons.Methanone, (2-hydroxy-4-methoxyphenyl)phenyl-; : (2-hydroxy-4-methoxyphenyl)(phenyl)methanone; (2-Hydroxy-4-methoxyphenyl)- phenylmethanone; (2-Hydroxy-4-methoxyphenyl)-phenylmethanone; (2-Hydroxy-4-methoxyphenyl)phenylmethanone; 2-benzoyl-5-methoxyphenol; 2-Hydroxy-4-methoxy benzophenone; Benzophenone, 2-hydroxy-4-methoxy-; Benzophenone-3; Eversorb 11; Speedblock UV-9; La benzophénone-3 est utilisée comme filtres UV dans des crèmes solaires et des produits cosmétiques, mais aussi dans la production d'insecticides, de produits chimiques agricoles et de produits pharmaceutiques, ainsi que comme additif pour les plastiques (incluant les emballages alimentaires), les matériaux de revêtement et les adhésifs. Lorsqu’appliquée sur la peau, la benzophénone-3 est absorbée efficacement avant d’être métabolisée et excrétée rapidement dans l’urine sous forme de métabolites conjugués. L’alimentation peut également être une source d’exposition importante à la benzophénone-3. En effet elle est parfois utilisée comme additif alimentaire, ou présente dans l’emballage d’où elle peut migrer vers l’aliment. La benzophénone-3 est suspectée appartenir au groupe des perturbateurs endocriniens, c’est-à-dire qu’elle serait capable d’interagir avec le système endocrinien pouvant dès lors causer des effets néfastes pour la santé. Le dosage urinaire de la benzophénone-3 glucuroconjuguée permet une estimation de l’exposition récente, ce qui est un bon indicateur des pratiques individuelles à modifier si l’on souhaite réduire la charge corporelle en polluants chimiques.s; Benzophenone-3(BP3); Escalol 567; (2-Hydroxy-4-methoxyphenyl)(phenyl)methanon [German] ;(2-Hydroxy-4-methoxyphenyl)(phenyl)methanone ; (2-Hydroxy-4-méthoxyphényl)(phényl)méthanone [French] ; 131-57-7 [RN]; 205-031-5 [EINECS]; 2-hydroxy-4-methoxy benzophenone; 2-Hydroxy-4-methoxybenzophenone;2-hydroxy-4-methoxyphenyl phenyl ketone; Benzophenone, 2-hydroxy-4-methoxy-; BENZOPHENONE-3; Methanone, (2-hydroxy-4-methoxyphenyl)phenyl- oxibenzona [Spanish] oxybenzone [USAN] [Wiki] oxybenzone [French] oxybenzonum [Latin] Uvinul M-40 оксибензон [Russian] أوكسيبانزون [Arabic] 羟苯甲酮 [Chinese] (2-hydroxy-4-methoxyphenyl)-phenylmethanone (2-Hydroxy-4-methoxyphenyl)phenylmethanone (2-Hydroxy-4-methoxy-phenyl)-phenyl-methanone [131-57-7] 1-(cyclopropylcarbonyl)-N-(4-ethoxyphenyl)-3,3-dimethylindoline-5-sulfonamide 14375-37-2 [RN] 153859-73-5 [RN] 2-Benzoyl-5-methoxyphenol 2-HYDROXY-4-METHOXYBENZOPHE 2-hydroxy-4-methoxy-benzophenone 2-Hydroxy-4-Methoxybenzophenone (en) 2-HYDROXY-4-METHOXYBNZOPHENONE 4-Methoxy-2-hydroxybenzophenone Advastab 45 Anuvex Benzoic acid, 4-(aminomethyl)- (9CI) Benzophenone 3 Benzophenone-3 (Bp-3) Chimassorb 90 Cyasorb UV 9 cyclohexa-3,5-diene-1,2-dione; (2-hydroxy-4-methoxyphenyl)-phenylmethanone D05309 DB01428 DuraScreen EINECS 205-031-5 Escalol 567 Eusolex 4360 Eusolex 4360;Escalol 567;KAHSCREEN BZ-3;Benzophenone 3 Eusolex-4360 Neo heliopan BB Ongrostab HMB Oprea1_174131 oxibenzona [Portuguese] Oxybenzon OXYBENZONE|2-BENZOYL-5-METHOXYPHENOL Pharmakon1600-01500451 Prestwick2_000887 Prestwick3_000887 PreSun 15 PreSun 46 Solaquin Solbar Spectra-sorb UV 9 SPECTRUM1500451 Spectrum5_001337 ST029243 Sunscreen UV-15 Syntase 62 UF 3 UV 9 Uvinul 40 Uvinul 40 (TN) Uvinul 9 Uvinul M 40 Uvinul M40 Uvistat 24 WLN: 1OR CQ DVR
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);
Oxybenzone ( BENZOPHENONE-3)
COCAMIDOPROPYLAMINE OXIDE, N° CAS : 68155-09-9, Nom INCI : COCAMIDOPROPYLAMINE OXIDE, N° EINECS/ELINCS : 268-938-5/931-324-9, Classification : Tensioactif amphotère; Agent nettoyant : Aide à garder une surface propre. Sinergiste de mousse : Améliore la qualité de la mousse produite en augmentant une ou plusieurs des propriétés suivantes: volume, texture et / ou stabilité. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Hydrotrope : Augmente la solubilité d'une substance qui est peu soluble dans l'eau.. Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : N-oxyde de N-((diméthylamino)-3 propyl) coco amides Oxyde de cocamidopropylamine Oxyde de cocamidopropyldiméthylamine Noms anglais : (COCAMIDOPROPYL)DIMETHYLAMINE OXIDE 3-(N,N-DIMETHYLAMINO)PROPYL COCOAMIDO AMINE OXIDE 3-COCOAMIDOPROPYL DIMETHYLAMINE OXIDE AMIDES, COCO, N-(3-(DIMETHYLAMINO)PROPYL), N-OXIDE COCAMIDOPROPYLDIMETHYLAMINE OXIDE N,N-DIMETHYL-N-(3-(COCONUT OIL ALKYL)AMIDOPROPYL)AMINE OXIDE N,N-DIMETHYL-N-(3-COCAMIDOPROPYL)AMINE OXIDE
Oxyde de cocamidopropylamine ( COCAMIDOPROPYLAMINE OXIDE)
Oxyde de zinc, Synonymes : Blanc de zinc, Monoxyde de zinc, Blanc permanent, C.I. 77947, C.I. pigment white 4, No CAS 1314-13-2, No ECHA 100.013.839, No CE 215-222-5, L’oxyde de zinc est un composé chimique d'oxygène et de zinc, corps ionique de formule chimique ZnO. Il est utilisé dans de nombreuses applications, telles que la fabrication de verres, de céramiques, dans la formation d'eugénate, dans la composition d'aliments et de crèmes solaires.Ce pigment ZnO sert dans l'industrie verrière et céramique à la préparation des verres blancs opaques et des émaux. Il entre aussi directement dans la composition des ferrites.Il s'agit d'un produit de l'industrie pharmaceutique et cosmétique, antiseptique connu bien avant le xixe siècle, où les chimistes pharmaciens s'occupaient de sa préparation. Il était employé en poudre, ou encore incorporé à des onguents ou des pommades pour les affections de la peau. Dans les années 1880, l'oxyde de zinc était employé sur la peau en tant qu'anti-transpirant, car il neutralise les productions acides tout en détruisant le plus grand nombre de bactéries présentes sur la peau. Il apporte encore une protection contre les brûlures, il peut être utilisé dans les préparations de ciment dentaire. Il sert à fabriquer des savons de zinc, utilisés comme siccatifs ou fongicides. Avec le dioxyde de titane, l'oxyde de zinc reste une charge opacifiante et protectrice des crèmes solaires. C'est une charge active dans l'industrie du caoutchouc et celle des pneumatiques. L'oxyde de zinc favorise la cinétique de vulcanisation. L'oxyde de zinc est un composant essentiel à la préparation de formulation ayant comme forme galénique la poudre. Il est à noter que le ZnO peut irriter gravement les mamelons et les parties de la peau ayant le moins de kératine en induisant une apoptose des cellules de ces régions.Zinc oxide; cink-oxid (hu); cinka oksīds (lv); cinko oksidas (lt); cinkov oksid (hr); ossido di zinco (it); oxid de zinc (ro); oxid zinečnatý (cs); oxid zinočnatý (sk); oxyde de zinc (fr); Sinkkioksidi (fi); sinkoksid (no); tlenek cynku (pl); Tsinkoksiid (et); zinkoxid (da);zinkoxide (nl); óxido de cinc (es); óxido de zinco (pt); οξείδιο του ψευδαργύρου (el);цинков окис (bg); Zinc oxide (ZnO), çinko oksit, çinkooksit, çinko oksid, çinkooksid,cinko oksit, cinko oksid. : Zinc oxide ; zinc oxide; Oxo zinc; Oxozinc; Reaction mass of 1309-48-4 and 7631-86-9; Reaction mass of 1313-13-9 and 7758-99-8; Reaction mass of 13463-67-7 and 14807-96-6 and 21645-51-2 and 68037-59-2; UPV8; zin oxide; Zinc (II) oxide; Zinc oxide (CI 77947); Zinc oxide (CI 77947) ; zinc oxide - poussières de fusion; zinc oxide / zinkoxid; Zinc Oxide Powder; Zinc oxide, ZnO; Zinc oxygen(2-); Zinc(II) oxide; Zinc(II)oxide; Zinci oxidum; zincoxide; OXIDO DE ZINC; zinc monoxide
Oxyde de zinc
ZINC OXIDE N° CAS : 1314-13-2 - Oxyde de zinc Interdit dans les cosmétiques en spray Origine(s) : Minérale Autres langues : Ossido di zinco, Zinkoxid, Óxido de zinc Nom INCI : ZINC OXIDE Nom chimique : Zinc oxide (CI 77947) N° EINECS/ELINCS : 215-222-5 Potentiel Comédogène (pc) : 1 Classification : Règlementé, Filtre UV minéral. Ses fonctions (INCI) Agent de foisonnement : Réduit la densité apparente des cosmétiques Colorant cosmétique : Colore les cosmétiques et/ou confère une couleur à la peau Agent de protection de la peau : Aide à éviter les effets néfastes des facteurs externes sur la peau Absorbant UV : Protège le produit cosmétique contre les effets de la lumière UV Filtre UV : Permet de filtrer certains rayons UV afin de protéger la peau ou les cheveux des effets nocifs de ces rayons.
Oxyde d'étain
Hydrocarbon waxes (petroleum) CAS NO:64742-33-2
OXYTOCIN
SYNONYMS Alpha-hypophamine;Atonin O;Atonin O, 3-L-isoleucine-8-L-leucine-;Di-sipidin;Endopituitrina;Glycinamide, L-cysteinyl-L-tyrosyl-L-isoleucyl-L-glutaminyl-L-asparaginyl-L-cysteinyl-L-prolyl-L-leucyl-, cyclic (1→6)-disulfide;Hyphotocin;Intertocine S;L-Cysteinyl-L-tyrosyl-L-isoleucyl-L-glutaminyl-L-asparaginyl-L-cysteinyl-L-prolyl-L-leucylglycinamide cyclic (1→6)-disulfide;Nobitocin S;Orasthin;oxitocina (Spanish) ;Oxystin;Oxytocin (English, German);Oxytocine (French) CAS NO:50-56-6
OZOCERITE WAX
earth wax; ozocerite; ozokerite wax; Hydrocarbon waxes (petroleum) CAS NO: 64742-33-2
Ozokerite
ozokerite, Cas : 64742-33-2 / 8021-55-4, EC : 265-134-6, L’ozokérite ou ozocérite , autrefois appelé earthwax (cire de terre) est une roche naturellement odorante et ayant la consistance d'une cire (en raison de sa teneur en Paraffine. Il existe de nombreux gisements dans le monde de cet hydrocarbure naturel1. Il s'agit d'une roche riche en carbone fossile constituée d'un mélange naturel de paraffines à longue chaîne et parfois classé dans les huiles minérales. On nomme parfois aussi (mais improprement) ozocérite une « cire » extraite (par traitement physicochimique) de la lignine
Ozokérite MD
p-amino benzoic acid; p-aminobenzoate; p-aminobenzoic acid; p-amino-Benzoic acid; para-aminobenzoic acid; Vitamin BX; Vitamin H1; PABA, N° CAS : 150-13-0, Nom INCI : PABA, Nom chimique : 4-Aminobenzoic acid, N° EINECS/ELINCS : 205-753-0. Noms français : 4-Aminobenzoic acid; 4-CARBOXANILINE; ACIDE AMINO-4 BENZOIQUE; Acide amino-4 benzoïque; Acide aminobenzoïque (para-); Acide p-aminobenzoique; Acide para-aminobenzoique; BENZOIC ACID, 4-AMINO-; BENZOIC ACID, P-AMINO-; p-Aminobenzoic acid; P-CARBOXANILINE; P-CARBOXYPHENYLAMINE. Noms anglais : 4-Aminobenzoic acid. Utilisation et sources d'émission: Fabrication de produits qui préviennent les brûlures causées par le soleil. Ses fonctions (INCI). Agent d'entretien de la peau : Maintient la peau en bon état. Non classé : Non classé; 150-13-0 [RN]. 205-753-0 [EINECS]; 471605 [Beilstein]; 4-Aminobenzoesäure [German] ; 4-Aminobenzoic Acid; 4-Aminobenzoic acid ; 4-aminophenylcarboxylic acid ;4-Carboxyphenylamine; Acide 4-aminobenzoïque [French] ; Acido p-aminobenzoico [Italian]; aminobenzoic acid [USP]; Aniline-4-carboxylic acid; Anti-Gray-hair Factor; Benzoic acid, 4-amino- ; Kyselina p-aminobenzoova ; PABA; p-amino benzoic acid; p-aminobenzoate; p-aminobenzoic acid; p-amino-Benzoic acid; para-aminobenzoic acid; Vitamin BX; Vitamin H1; ZR DVQ [WLN]; Actipol; Anticantic vitamin; Antichromotrichia factor; Pabagel ; Trochromogenic factor; γ-Aminobenzoic acid; 1-Amino-4-carboxybenzene; 4-Aminobenzoesaeure; 4-azaniumylbenzoate; 4-Carboxyaniline; ABEE; Acidum paraminobenzoicum; AMBEN; Anticanitic vitamin; Anti-chromotrichia factor; Bacterial vitamin H1;Benzoic acid, p-amino-; Chromotrichia factor; Hachemina; PAB; Pabacyd; Pabafilm; Pabamine; Pabanol; p-Aminobenzoesaeure; Papacidum; Para amino benzoic acid; para-amino benzoic acid; Paraminobenzoic Acid; Paraminol; Paranate; p-Carboxyaniline; p-Carboxyphenylamine; Potaba ; Romavit; Sunbrella ; Trichochromogenic factor; γ-Aminobenzoate; γ-Aminobenzoic acid; 对氨基苯甲酸 [Chinese]
Ökaliptus Yağı
EUCALYPTUS OIL ; eucalyptus globulus leaf oil; eucalyptus 80/85%; eucalyptus globulus oil; eucalyptus ess. oil (for fragrance) (Robertet); hydroessential eucalyptus; hydroessential eucalyptus; eucalyptus forte CAS NO:8000-48-4
P.E.G 4000/6000/8000
SYNONYMS PEG; Macrogol; Polyoxyethlene; Aquaffin; Nycoline;alpha-hydro-omega-hydroxypoly(oxy-1,2-ethanediyl); polyethylene glycols; Poly Ethylene Oxide; Polyoxyethylene; Polyglycol; 1,2-ethanediol Ehoxylated; Polyoxyethylene ether; Polyoxyethylene; Poly(ethylene glycol); CAS NO:25322-68-3
PABA ( Acide 4-aminobenzoïque)
Polyaluminum chlorohydrate; Polyaluminum hydroxychloride CAS NO:1327-41-9
PAC (Polyaluminium Chlorohydrate)
Polyaluminum chlorohydrate; Polyaluminum hydroxychloride CAS NO:1327-41-9
Paçuli Yağı
PATCHOULI OIL ; patchouli oil; patchouli heart ; patchouli purecoeur essential oil; pogostemon patchouli oil; patchouli fraction oil; volatile oil obtained from the leaves of the patchouli, pogostemon cablin, labiatae CAS NO:8014-09-3
PALATINOL IC
Palatinol IC представляет собой пластификатор без запаха с молекулярной формулой C16H22O4.
Palatinol IC представляет собой эфир фталевой кислоты, который представляет собой диэфир, полученный формальной конденсацией карбоксильных групп фталевой кислоты с двумя молекулами изобутанола.
Palatinol IC принадлежит к классу органических соединений, известных как эфиры бензойной кислоты.

Номер CAS: 84-69-5
Номер ЕС: 201-553-2
Химическая формула: C16H22O4.
Молярная масса: 278,348 г·моль−1

Бис(2-метилпропил)бензол-1,2-дикарбоксилат, Диизобутилфталат, Ди-изобутилфталат, Ди(изобутил)фталат, Диизобутиловый эфир фталевой кислоты, 1,2-бензолдикарбоновая кислота, Бис(2-метилпропил) )эфир, ди(изобутил)1,2-бензолдикарбоксилат, изобутил-О-фталат, DIBP, DiBP, Palatinol IC, ДИИЗОБУТИЛФТАЛАТ, 84-69-5, DIBP, Palatinol IC, изобутилфталат, диизобутиловый эфир фталевой кислоты, гексаплаз M /1B, Kodaflex DIBP, диизобутилфталат, фталевая кислота, диизобутиловый эфир, ди(изобутил)фталат, 1,2-бензолдикарбоновая кислота, бис(2-метилпропиловый) эфир, диизобутиловый эфир киселина фталова, NSC 15316, бис (2-метилпропил)фталат, изобутил-о-фталат, 1,2-бензолдикарбоновая кислота, 1,2-бис(2-метилпропил) эфир, DTXSID9022522, ди-2-метилпропилфталат, ди-1-бутилфталат (DIBP) , IZ67FTN290, CHEBI:79053, NSC-15316, Hatcol DIBP, DTXCID602522, бис(2-метилпропиловый) эфир 1,2-бензолдикарбоновой кислоты, ди(2-метилпропиловый) эфир 1,2-бензолдикарбоновой кислоты, бис- изобутиловый эфир, CAS-84-69-5, SMR000112470, диизобутилфталат, CCRIS 6193, HSDB 5247, AI3-04278 (USDA), EINECS 201-553-2, BRN 2054802, UNII-IZ67FTN290, AI3-04278, изобутил фталат (VAN), бис(2-метилпропил)бензол-1,2-дикарбоксилат, EC 201-553-2, диизобутилфталат, 99%, SCHEMBL42787, 4-09-00-03177 (Справочник Beilstein), MLS000516002, MLS002152902 , BIDD:ER0640, 1, бис(2-метилпропил) эфир, CHEMBL1370662, HMS2269D07, NSC15316, Tox21_202429, Tox21_300612, MFCD00026480, AKOS015837516, диизобутилфталат (ACD/название 4.0), WL Н: 1Y1&1OVR BVO1Y1&1, NCGC00091360-01, NCGC00091360-02 , NCGC00091360-03, NCGC00091360-04, NCGC00254487-01, NCGC00259978-01, FT-0689059, NS00010605, P0298, Q162259, 1,2-бис(2-метилпропил)бензол-1,2-дикарбоксилат , J-503794, 1 Ди(2-метилпропил) эфир 2-бензолдикарбоновой кислоты, бис-изобутиловый эфир фталевой кислоты 10 мкг/мл в циклогексане, диизобутилфталат, сертифицированный эталонный материал, TraceCERT(R), 1,2-бензолдикарбоновая кислота, бис(2- метилпропиловый эфир, DIBP, ди(изобутил)фталат, диизобутилфталат, диизобутиловый эфир киселина фталова [Чехия], Hatcol DIBP, Hexaplas M/1B, изобутилфталат, Kodaflex DIBP, Palatinol IC, фталевая кислота, диизобутиловый эфир , Фталоилдихлорид, MFCD01861606, EINECS 201-553-2, Фталилхлорид, бис(2-метилпропил)бензол-1,2-дикарбоксилат, Фталевой дихлорид, 1,2-бензолдикарбонилдихлорид, тетрафталоилхлорид, Дихлорид фталевой кислоты, диизобутил 1, 2-бензолдикарбоксилат, 1,2-бензолдикарбоновая кислота, бис(2-метилпропил) эфир, ди-1-бутилфталат (ДИБФ), диизобутилфталат, фталоилхлорид, фталилдихлорид, бензол-1,2-дикарбонилдихлорид, фталевой хлорид, Диизобутиловый эфир 1,2-бензолдикарбоновой кислоты, бис(2-метилпропил) эфир 1,2-бензолдикарбоновой кислоты, AI3-04278, бисофлекс ДИБА, бисофлекс ДИБФ, ди(изобутил)1,2-бензолдикарбоксилат, ДИБФ (=диизобутилфталат) ), дипласт B, хаткол DIBP, гексаплас M 18, гексаплас M/1B, гексаплас MIB, изобутилфталат, jayflex DIBP, кодафлекс DIBP, моллан L, диизобутиловый эфир фталевой кислоты, вестинол IB), DBP, АРАЛДИТОВАЯ СМОЛА, бутилфталат, N -БУТИЛФТАЛАТ, дибутилфталат, дибутил-о-фталат, ди-н-бутилфталат, дибутилфталат (DBP), диизобутилфталат (DIBP), дибутиловый эфир фталевой кислоты, ди-н-бутиловый эфир фталевой кислоты, дибутилфталат, аббревиатура , ДИ-Н-БУТИЛОВЫЙ ЭФИР ФТАЛЕВОЙ КИСЛОТЫ, ФТАЛЕВАЯ КИСЛОТА, БИС-БУТИЛОВЫЙ ЭФИР, дибутилбензол-1,2-дикарбоксилат, ДИБУТИЛОВЫЙ ЭФИР О-БЕНЗОЛДИКАРБОКСИЛЬНОЙ КИСЛОТЫ, ди-н-бутиловый эфир бензол-1,2-дикарбоновой кислоты, 1, 2-Бензолдикарбоновая кислота, 1,2-бис(2-метилпропил) эфир, 1,2-Бензолдикарбоновая кислота, бис(2-метилпропил) эфир, 1,2-Бензолдикарбоновая кислота, ди(2-метилпропил) эфир, Бис(2) -метилпропил)фталат, ди-2-метилпропилфталат, DIBP, диизобутилфталевая кислота, Hexaplas M/1B, изобутилфталат,

Palatinol IC — органическое соединение, используемое в качестве пластификатора при производстве пластмасс и резины.
Palatinol IC представляет собой бесцветную маслянистую жидкость со слабым запахом.

Palatinol IC представляет собой эфир фталевой кислоты, который представляет собой тип химического соединения, полученного из фталевой кислоты.
Palatinol IC представляет собой прозрачную жидкость.

Palatinol IC представляет собой бесцветную маслянистую жидкость со слабым эфирным запахом.
Palatinol IC зарегистрирован в соответствии с Регламентом REACH и производится и/или импортируется в Европейскую экономическую зону в объеме ≥ 1 тонны в год.

Palatinol IC представляет собой эфир фталевой кислоты, который представляет собой диэфир, полученный формальной конденсацией карбоксильных групп фталевой кислоты с двумя молекулами изобутанола.
Palatinol IC представляет собой маслянистую бесцветную жидкость со слабым эфирным запахом.

Palatinol IC представляет собой пластификатор без запаха с молекулярной формулой C16H22O4.
Palatinol IC представляет собой эфир фталевой кислоты, который представляет собой диэфир, полученный формальной конденсацией карбоксильных групп фталевой кислоты с двумя молекулами изобутанола.

Palatinol IC растворим в этаноле, эфире, ацетоне и бензоле.
Palatinol IC принадлежит к классу органических соединений, известных как эфиры бензойной кислоты.
Это эфирные производные бензойной кислоты.

Palatinol IC получают путем этерификации изобутанола и фталевого ангидрида.
Palatinol IC представляет собой пластификатор без запаха и обладает превосходной термо- и светостойкостью.

Palatinol IC — самый дешевый пластификатор нитрата целлюлозы.
Palatinol IC имеет более низкую плотность и температуру замерзания, чем DBP.

Palatinol IC имеет свойства, аналогичные дибутилфталату, и может использоваться в качестве его заменителя.
Palatinol IC представляет собой маслянистую бесцветную жидкость со слабым эфирным запахом.

Palatinol IC плотнее воды.
Palatinol IC нерастворим в воде.

Palatinol IC представляет собой эфир фталевой кислоты, который представляет собой диэфир, полученный формальной конденсацией карбоксильных групп фталевой кислоты с двумя молекулами изобутанола.
Palatinol IC играет роль пластификатора, тератогенного агента и модулятора PPAR.

Palatinol IC представляет собой сложный эфир фталевой кислоты и диэфир.
Palatinol IC функционально связан с изобутанолом.

Palatinol IC представляет собой пластификатор без запаха и обладает превосходной термо- и светостойкостью.
Palatinol IC — самый дешевый пластификатор нитрата целлюлозы.
Palatinol IC имеет более низкую плотность и температуру замерзания, чем DBP (дибутилфталат, номер CAS: 84-74-2).

Palatinol IC может заменить дибутилфталат (DBP) в большинстве, если не во всех, применениях.
Поскольку Palatinol IC химически не связан с полимерной матрицей, он может выделять газ или выделяться при контакте с жидкостями и жиром.
В окружающей среде Palatinol IC разлагается относительно быстро.

Palatinol IC совместим с ПВХ.
Palatinol IC представляет собой эфир фталевой кислоты, имеющий структурную формулу C6H4(COOCH2CH(CH3)2)2.

Palatinol IC образуется путем этерификации изобутанола и фталевого ангидрида.
Когда дело доходит до выведения, Palatinol IC сначала превращается в гидролитический моноэфир моноизобутилфталат (МИБФ).

Основным путем выведения является моча, при этом экскреция с желчью отмечается в незначительных количествах.
Palatinol IC имеет более низкую плотность и температуру замерзания, чем родственное соединение дибутилфталат (DBP).

Palatinol IC может продаваться как в чистом виде, так и в виде компонента смесей с другими фталатными пластификаторами или химическими веществами.
Примерами являются диоктилфталат (DOP), диизононилфталат (DINP) или бис(2-этилгексил)фталат (DEHP).
Palatinol IC – это натуральный продукт, обнаруженный в Artemisia baldshuanica, Lythrum salicaria и других организмах, о которых имеются данные.

Использование Palatinol IC:
Palatinol IC используется потребителями, в изделиях, профессиональными работниками (широко распространенное применение), при составлении рецептур или переупаковке, на промышленных объектах и в производстве.
Palatinol IC используется в следующих продуктах: покрытиях, шпатлевках, шпаклевках, штукатурках, глине для лепки и полимерах.

Другие выбросы Palatinol IC в окружающую среду могут происходить при: использовании внутри помещений и при использовании на открытом воздухе, приводящем к попаданию в материалы или на них (например, связующее вещество в красках и покрытиях или клеях).
Выброс Palatinol IC в окружающую среду может происходить при промышленном использовании: при производстве изделий, составлении смесей и веществ в закрытых системах с минимальным выбросом.
Другие выбросы Palatinol IC в окружающую среду, вероятно, происходят в результате: использования внутри помещений, использования вне помещений, приводящего к включению в материалы или на них (например, связующего вещества в красках и покрытиях или клеях), использования вне помещений в долговечных материалах с высокой скоростью высвобождения. (например, шины, обработанные деревянные изделия, обработанные ткани и ткани, тормозные колодки в грузовиках или легковых автомобилях, шлифовка зданий (мосты, фасады) или транспортных средств (суда)) и использование внутри помещений с долговечными материалами с высокой скоростью выделения (например, выделение из ткани, текстиль при стирке, удалении внутренних красок).

Palatinol IC можно найти в сложных изделиях, не предназначенных для выпуска: транспортных средствах, машинах, механических устройствах и электрических/электронных изделиях (например, компьютерах, фотоаппаратах, лампах, холодильниках, стиральных машинах), а также электрических батареях и аккумуляторах.
Palatinol IC можно найти в продуктах, содержащих материалы на основе: пластика (например, упаковка и хранение пищевых продуктов, игрушки, мобильные телефоны), металла (например, столовые приборы, кастрюли, игрушки, украшения), резины (например, шины, обувь, игрушки), кожи (например, например, перчатки, обувь, сумки, мебель) и дерево (например, полы, мебель, игрушки).

Palatinol IC используется в следующих продуктах: покрытиях, шпатлевках, шпаклевках, штукатурках, пластилине, полимерах, клеях и герметиках.
Palatinol IC используется в следующих областях: составление смесей и/или переупаковка.

Palatinol IC используется для производства: пластмассовых изделий, минеральных продуктов (например, штукатурки, цемента), а также машин и транспортных средств.
Выброс Palatinol IC в окружающую среду может происходить при промышленном использовании: при производстве изделий, веществ в закрытых системах с минимальным выбросом и при промышленной абразивной обработке с низкой скоростью выброса (например, резка текстиля, резка, механическая обработка или шлифовка металла).

Другие выбросы Palatinol IC в окружающую среду могут происходить при: использовании внутри помещений и при использовании на открытом воздухе, приводящем к попаданию в материалы или на них (например, связующее вещество в красках и покрытиях или клеях).
Palatinol IC используется в следующих продуктах: покрытиях, шпатлевках, шпаклевках, штукатурках, пластилине и полимерах.

Palatinol IC имеет промышленное применение, приводящее к производству другого вещества (использование промежуточных продуктов).
Выброс Palatinol IC в окружающую среду может происходить в результате промышленного использования: при составлении смесей и в составе материалов.
Palatinol IC имеет промышленное применение, приводящее к производству другого вещества (использование промежуточных продуктов).

Palatinol IC используется в следующих областях: составление смесей и/или переупаковка.
Palatinol IC используется для производства: химических веществ.
Выброс Palatinol IC в окружающую среду может происходить при промышленном использовании: как промежуточный этап при дальнейшем производстве другого вещества (использование полупродуктов) и при производстве изделий.

Выброс Palatinol IC в окружающую среду может происходить в результате промышленного использования: производства Palatinol IC.
Palatinol IC — пластификатор, используемый в потребительских целях.
продукты в качестве ингредиента-заменителя ди-н-бутилфталата (DBP) из-за структурного сходства.

Таким образом, присутствие Palatinol IC в продуктах может увеличиться.
Palatinol IC — пластификатор, используемый в пластике из поливинилхлорида (ПВХ) для повышения гибкости.

Palatinol IC можно использовать вместо дибутилфталата из-за более низких производственных затрат.
Кроме того, Palatinol IC можно использовать в таких областях, как чернила, покрытия, лаки и клеи.

Palatinol IC действует как пластификатор.
Palatinol IC можно использовать в качестве замены дибутилфталата из-за более низких производственных затрат.

Palatinol IC используется в пластике из поливинилхлорида (ПВХ) для повышения гибкости.
Palatinol IC используется в качестве пластификатора.

Palatinol IC используется в красках, лаках и лаках.
Palatinol IC также используется в бумажной и целлюлозной промышленности, а также в производстве картона, химикатов, полимеров, клеев, пластификаторов и регуляторов вязкости.

Palatinol IC получают путем этерификации изобутанола и фталевого ангидрида.
Palatinol IC представляет собой пластификатор без запаха и обладает превосходной термо- и светостойкостью.

Palatinol IC — самый дешевый пластификатор нитрата целлюлозы.
Palatinol IC имеет более низкую плотность и температуру замерзания, чем DBP.

Palatinol IC имеет свойства, аналогичные дибутилфталату, и может использоваться в качестве его заменителя.
Palatinol IC представляет собой бесцветную прозрачную маслянистую жидкость, используемую в качестве альтернативы DBP (дибутилфталату).

Palatinol IC используется в красках на основе нитроцеллюлозы и алкидных смол.
Palatinol IC получают путем этерификации изобутанола и фталевого ангидрида.

Palatinol IC представляет собой пластификатор без запаха и обладает превосходной термо- и светостойкостью.
Palatinol IC — самый дешевый пластификатор нитрата целлюлозы.

Palatinol IC имеет более низкую плотность и температуру замерзания, чем DBP.
Palatinol IC имеет свойства, аналогичные дибутилфталату, и может использоваться в качестве его заменителя.

Palatinol IC — пластификатор, который используется в нитроцеллюлозе, красках на основе алкидных смол, чернилах, покрытиях, лаках и клеях.
Из-за более низких производственных затрат Palatinol IC используется в качестве альтернативы DBP (дибутилфталату).

Palatinol IC представляет собой пластификатор, который используется с различными полимерами, такими как полиакрилат, дисперсии полиацетата, ацетат целлюлозы, нитроцеллюлоза, полиуретан и поливинилбутират.
Palatinol IC часто используется в сочетании с другими фталатами.

Palatinol IC в большинстве случаев используется в качестве заменителя DBP.
Palatinol IC используется при пластификации ПВХ, производстве красок, печатных красок и клеев.

Некоторые области применения Palatinol IC включают: напольные покрытия, краски, промышленные клеи, лаки, печатные краски, гидравлические жидкости и смазочные материалы.
Palatinol IC используется в различных продуктах, включая упаковку пищевых продуктов, медицинские устройства и игрушки.

Palatinol IC используется в качестве пластификатора при производстве гибких изделий из ПВХ, таких как изоляция проводов и кабелей, виниловые полы, клеи и покрытия.
Palatinol IC также используется в производстве лаков, печатных красок и синтетической кожи.

Palatinol IC представляет собой пластификатор на основе диалкилфталатного эфира фталата, который можно использовать в качестве заменителя дибутилфталата.
Palatinol IC, как и другие фталаты, обладают генотоксическим действием, и исследования показали увеличение его моноэфирного метаболита в моче человека с течением времени.

Palatinol IC является одним из основных широко используемых пластификаторов.
Palatinol IC можно использовать в качестве пластификатора целлюлозной смолы, виниловой смолы, NBR и хлорированного каучука.

Подобно Palatinolу IC, он обладает превосходной растворимостью, диспергируемостью и адгезией.
Palatinol IC имеет хорошую совместимость с пигментами.

Palatinol IC можно использовать для окраски пленок, изделий из искусственной кожи и пластика.
Palatinol IC также можно использовать в качестве смягчителя натурального и синтетического каучука для повышения устойчивости изделий.

Palatinol IC можно использовать вместо DBP.
Palatinol IC представляет собой сложный эфир фталевой кислоты, который представляет собой диэфир, полученный формальной конденсацией карбоксильных групп фталевой кислоты с двумя молекулами изобутанола. Palatinol IC считается специальным пластификатором, который слишком летуч для использования в поливинилхлориде (ПВХ).

Palatinol IC часто комбинируют с другими фталатами.
Palatinol IC обладает хорошей термо- и светостабильностью и использовался в качестве пластификатора для нитроцеллюлозы (самый дешевый пластификатор для нитрата целлюлозы), эфира целлюлозы, а также дисперсий полиакрилата и полиацетата.

Palatinol IC используется в лаках для ногтей, косметике, смазочных материалах, напольных коврах, гобеленах, средствах для ухода за одеждой, резиновых стоматологических инструментах, в качестве стабилизатора топлива, в лаках и лаках для кожи, в качестве добавки к бетону, в качестве корректирующего агента для пигментов красок на основе хромата свинца, взрывчатые вещества, производство лаков и применение метилметакрилата.

Palatinol IC также используется в печатных красках для бумаги и упаковки.
Поскольку Palatinol IC обладает свойствами, аналогичными дибутилфталату (DBP), Palatinol IC можно использовать в качестве заменителя DBP.

Palatinol IC в основном используется в качестве нитроцеллюлозы, ацетата целлюлозы, поливинилхлорида и других пластификаторов; Реагенты общего химического анализа для стационарной жидкости газовой хроматографии.
Palatinol IC используется в качестве растворителей, пестицидов, пластификаторов.

Palatinol IC имеет свойства, аналогичные дибутилфталату, и может использоваться в качестве его заменителя.
Palatinol IC синтезируется химической реакцией фталевой кислоты с изобутиловым спиртом.

Palatinol IC представляет собой пластификатор с коагулирующими свойствами, который использовался с различными полимерами, например, с полиакрилатом, дисперсиями полиацетата, ацетатом целлюлозы, нитратом целлюлозы, этилцеллюлозой, полиуретаном и поливинилбутиратом.
В сочетании с другими пластификаторами Palatinol IC применялся в качестве гелеобразователя при переработке так называемых пластизолей.

Palatinol IC присутствует, например, в напольных покрытиях, клеях, лаках, чернилах, гидравлических жидкостях и смазочных материалах.
Palatinol IC использовался в качестве маркера в топливе для целей налогообложения, а также в производстве титановых катализаторов.
Palatinol IC можно использовать в качестве замены дибутилфталата из-за более низких производственных затрат.

Palatinol IC используется в клеях.
Palatinol IC можно использовать в качестве компонента в рецептурах некоторых продуктов, включая клеи, краски, покрытия и смазочные материалы.

Этот и другие фталаты используются в качестве пластификаторов благодаря своей гибкости и долговечности.
Они содержатся во многих промышленных и бытовых товарах, таких как лаки, лаки для ногтей и косметика.

Промышленность использует:
Palatinol IC используется в качестве пластификатора в ряде пластиковых и резиновых материалов.
Palatinol IC имеет низкую летучесть, что делает его идеальным для использования в продуктах, требующих длительной гибкости, например, в автомобильных деталях, изоляции проводов и кабелей, а также в напольных покрытиях.
Palatinol IC плотный и нерастворимый в воде.

Пищевая промышленность:
Palatinol IC используется в качестве пластификатора в упаковочных материалах для пищевых продуктов, таких как пленки и листы поливинилхлорида (ПВХ).
Palatinol IC также используется в материалах, контактирующих с пищевыми продуктами, таких как клеи, покрытия и герметики.
Palatinol IC используется для улучшения гибкости, долговечности и прозрачности этих материалов.

Способ производства Palatinol IC:
Palatinol IC производится путем этерификации фталевого ангидрида и изобутанола в присутствии серной кислоты.
Palatinol IC синтезируется в процессе этерификации изобутанола и фталевого ангидрида в присутствии серной кислоты в качестве катализатора.

Синтез Palatinol IC:
Palatinol IC синтезируется путем реакции двойного нуклеофильного ацильного замещения между фталевым ангидридом и изобутанолом с использованием различных кислот в качестве катализатора, таких как серная кислота, сульфированный графен или хлорид железа (III).
Вода является побочным продуктом.
При использовании серной кислоты выход составляет 61%.

Оптимизация Palatinol IC:
Сульфированный графен представляет собой гетерогенный катализатор, который имеет ряд преимуществ перед традиционными жидкими кислотами, такими как серная кислота.
Сульфированный графен легко отделяется от реакционной смеси фильтрованием и может быть использован многократно без снижения активности.

Кроме того, сульфированный графен безвреден для окружающей среды, поскольку Palatinol IC не производит опасных отходов, которые обычно образуются при использовании традиционных жидких кислотных катализаторов.
Этот метод имеет выход 95%.

В качестве катализатора также можно использовать кислоты Льюиса, такие как FeCl3.
Процесс кислотного катализа Льюиса может проводиться при более низких температурах (50–100 ° C) и дает выход 86%.

Механизм дейс��вия Palatinol IC:

Путь PPARγ:
Эффекты воздействия Palatinol IC в основном реализуются за счет активации гамма-рецептора, активируемого пролифератором пероксисом (PPARγ).
PPAR представляют собой активируемые лигандами ядерные факторы транскрипции, семейство состоит из PPARα, PPARβ/δ и PPARγ.
Существует две изоформы PPARγ: PPARγ2 в основном присутствует в клетках жировой ткани, тогда как PPARγ1 обнаруживается во многих клетках, таких как клетки кишечника, головного мозга, кровеносных сосудов, а также в некоторых иммунных и воспалительных клетках.

Регуляция транскрипции посредством PPAR требует образования гетеродимера с рецептором ретиноида X (RXR).
При активации Palatinolом IC этот гетеродимер PPARγ/RXR связывается с последовательностью ДНК, называемой элементом ответа PPAR (PPRE).
Связывание транскрипционного фактора с этим ответным элементом может привести как к повышению, так и к понижению регуляции генов.

PPARγ участвует в метаболизме и хранении липидов, а также в метаболизме глюкозы за счет повышения чувствительности к инсулину, поэтому связывание Palatinol IC приводит к изменению уровней лептина и инсулина.
Palatinol IC также приводит к снижению регуляции белков, участвующих в выработке стероидов, что приводит к повышению уровня андрогенных гормонов.

Путь цитокин-цитокиновых рецепторов
Другим типом пути, на который влияет воздействие Palatinol IC, является путь цитокин-цитокиновый рецептор.
Затрагиваются два пути: суперсемейство рецепторов фактора некроза опухоли (TNFRSF) и путь рецептора пролактина, оба из которых влияют на сперматогенез.

Реакции Palatinol IC на окружающую среду:
Palatinol IC может подвергаться различным реакциям, которые могут повлиять на окружающую среду.

Примеры включают в себя:

Гидролиз:
Гидролиз Palatinol IC может осуществляться ферментами, бактериями и другими микроорганизмами в окружающей среде с образованием фталевой кислоты и изобутилового спирта.
Это может привести к разрушению и возможной деградации Palatinol IC в почве и водоснабжении.

Фотодеградация:
Palatinol IC может подвергаться фотодеградации под воздействием солнечного света.
Это может привести к образованию нескольких продуктов разложения, в том числе фталевой кислоты, изобутиральдегида и других альдегидов.

Биодеградация:
Palatinol IC может разлагаться микроорганизмами в почве и воде.
Это может превратить Palatinol IC в другие соединения, такие как фталевая кислота и различные производные изобутилового спирта.

Сорбция:
Palatinol IC может адсорбироваться или сорбироваться на частицах почвы и отложений, что может ограничивать подвижность и доступность Palatinol IC для биологического или химического разложения и реакций.

Окисление:
Palatinol IC может окисляться в присутствии озона или других активных форм кислорода.
Можно ожидать образования различных продуктов окисления, в том числе альдегидов, кетонов и карбоновых кислот.
Эти реакции могут влиять на стойкость, биоаккумуляцию и токсичность в окружающей среде, а также иметь последствия для здоровья человека и экосистем.

Матеболизм Palatinol IC:
При попадании в кровоток Palatinol IC быстро метаболизируется и выводится через мочу, при этом метаболиты достигают максимальной концентрации через 2–4 часа после приема.
Основным метаболитом Palatinol IC является моноизобутилфталат (МиБФ), который составляет 70% продуктов выведения.

MiBP может окисляться либо до 2OH-моноизобутилфталата (2OH-MiBP), либо до 3OH-моноизобутилфталата (3OH-MiBP), которые составляют 20% и 1% продуктов выведения соответственно.
Эти реакции, вероятно, катализируются цитохромом Р450 в печени.

Соотношение между MiBP и окисленными метаболитами меняется в зависимости от времени, прошедшего с момента воздействия.
Соотношение между MiBP и 2OH-MiBP, а также между MiBP и 3OH-MiBP демонстрирует аналогичную тенденцию.
Соотношения высокие, около 20-30:1, вскоре после воздействия и постепенно снижаются по мере того, как проходит время отдыха, примерно 2-5:1.

Таким образом, высокое соотношение окисленных метаболитов к моноэфирному метаболиту предполагает недавнее воздействие Palatinol IC, в течение нескольких часов после измерения, тогда как более низкое соотношение предполагает, что с момента воздействия прошло больше времени.
Помимо окисления, MiBP также может подвергаться реакции глюкуронидации, в результате чего образуется метаболит MiBP-глюкуронид.

История Palatinol IC:
В 1836 году французский химик Огюст Лоран окислил нафталин хромовой кислотой и создал фталевый ангидрид, из которого получают фталаты.
Фталаты, в том числе Palatinol IC, были впервые представлены в 1920-х годах для придания пластмассам большей гибкости, прозрачности и долговечности.

Их популярность возросла в 1931 году, когда поливинилхлорид (ПВХ) стал коммерчески доступным.
Из-за увеличения воздействия фталатов на человека в 1999 году Европейский Союз ограничил использование некоторых из них в детских игрушках.

Хранение Palatinol IC:
Palatinol IC следует хранить в прохладном, сухом и хорошо проветриваемом месте.
Palatinol IC следует хранить в металлическом барабане, из нержавеющей стали, алюминия или смолы, армированной полиэфиром.

Palatinol IC следует хранить отдельно от продуктов питания.
Palatinol IC следует хранить в контейнерах отдельно от сильных окислителей.

Обращение и хранение Palatinol IC:

Меры предосторожности для безопасного обращения:

Рекомендации по безопасному обращению:
Работа под капотом.

Гигиенические меры:
Немедленно смените загрязненную одежду.
Применяйте профилактическую защиту кожи.
Вымойте руки и лицо после работы с Palatinol IC.

Условия безопасного хранения, включая любые несовместимости:

Условия хранения:
Плотно закрыто.
Хранить в хорошо проветриваемом месте.
Храните взаперти или в месте, доступном только квалифицированным или уполномоченным лицам.

Стабильность и реакционная способность Palatinol IC:

Реактивность:
Palatinol IC реагирует с кислотами с выделением тепла вместе с изобутиловым спиртом и фталевой кислотой.
Palatinol IC может достаточно экзотермически реагировать с сильными окисляющими кислотами, вызывая воспламенение продуктов реакции.

Тепло также выделяется при взаимодействии с каустическими растворами.
Горючий водород образуется при смешивании с щелочными металлами и гидридами.
Palatinol IC может генерировать электростатические заряды при обращении с ним.

Химическая стабильность:
Palatinol IC химически стабилен при стандартных условиях окружающей среды (комнатная температура).

Возможность опасных реакций:
Данные недоступны

Меры первой помощи Palatinol IC:

Общий совет:
Покажите паспорт безопасности Palatinol IC лечащему врачу.

При вдыхании:

После ингаляции:
Свежий воздух.
Вызовите врача.

При попадании на кожу:
Немедленно снимите всю загрязненную одежду.
Промойте кожу водой/душем.
Проконсультируйтесь с врачом.

При попадании в глаза:

После зрительного контакта:
Промойте большим количеством воды.
Вызовите офтальмолога.
Снимите контактные линзы.

При проглатывании:

После глотания:
Немедленно дайте пострадавшему выпить воды (максимум два стакана).
Проконсультируйтесь с врачом.

Указание на необходимость немедленной медицинской помощи и специального лечения.
Данные недоступны

Меры пожаротушения Palatinol IC:

Подходящие средства пожаротушения:
Вода
Мыло
Углекислый газ (CO2)
Сухой порошок

Неподходящие средства пожаротушения:
Для этого вещества/смеси не установлены ограничения по огнетушащим веществам.

Дальнейшая информация:
Не допускайте попадания воды для пожаротушения в поверхностные воды или систему грунтовых вод.

Меры по случайному высвобождению Palatinol IC:

Экологические меры предосторожности:
Не допускайте попадания продукта в канализацию.

Методы и материалы для локализации и очистки:
Закройте дренажи.
Соберите, свяжите и откачайте пролитую жидкость.

Соблюдайте возможные ограничения по материалам.
Собирать осторожно с материалом, впитывающим жидкость.

Утилизируйте должным образом.
Очистите пораженное место.

Идентификаторы Palatinol IC:
Номер CAS: 84-69-5
Молекулярный вес: 278,34
Байльштайн: 2054802
Номер ЕС: 201-553-2
Номер леев: MFCD00026480
Химическая формула: C16H22O4.
Молярная масса: 278,348 г·моль−1
Внешний вид: Бесцветная вязкая жидкость.
Плотность: 1,038 г/см3
Температура плавления: -37 ° C (-35 ° F; 236 К)
Точка кипения: 320 ° C (608 ° F; 593 К)
Растворимость в воде: 1 мг/л при 20 °C.
журнал Р: 4.11
Давление пара: 0,01 Па при 20 °C.
Температура вспышки: 185 ° C (365 ° F; 458 К) куб.см.
Температура самовоспламенения: 400 ° C (752 ° F; 673 К)

Точка плавления: -37 °С.
Воспламеняемость: Горючий
Анализ: от 95,00 до 100,00.
Внесен в Кодекс пищевых химикатов: Нет
Температура кипения: 296,00 °С. @ 760,00 мм рт. ст.
Давление пара: 0,002000 мм рт. ст. при 25,00 °C. (стандартное восточное время)
Температура вспышки: 309,00 °F. TCC (153,90 °C) (оценка)
logP (н/б): 4,110
Растворим в: воде, 6,2 мг/л при 24°C (экспер.)
КАС: 84-74-2
ЭИНЭКС: 201-557-4
InChIKey: DOIRQSBPFJWKBE-UHFFFAOYSA-N
Молекулярная формула: C16H22O4.
Молярная масса: 278,34

Условия хранения: 2-8°C
Чувствительность: легко впитывает влагу.
Предел взрываемости: 0,47%, 236°F
Показатель преломления: n20/D 1,492 (лит.)
лей: MFCD00009441
Химическая формула: C16H22O4.
Средняя молекулярная масса: 278,344 г/моль.
Моноизотопная масса: 278,152 г/моль.
Регистрационный номер CAS: 84-69-5
Название ИЮПАК: 1,2-бис(2-метилпропил)бензол-1,2-дикарбоксилат.
Традиционное название: Palatinol IC.
УЛЫБКИ: CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C
Идентификатор InChI: 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
Ключ InChI: InChIKey=MGWAVDBGNNKXQV-UHFFFAOYSA-N

Свойства Palatinol IC:
Молекулярный вес: 278,34 г/моль
XLogP3: 4.1
Количество доноров водородной связи: 0
Количество акцепторов водородной связи: 4
Количество вращающихся облигаций: 8
Точная масса: 278,15180918 г/моль.
Моноизотопная масса: 278,15180918 г/моль.
Топологическая площадь полярной поверхности: 52,6Ų.
Количество тяжелых атомов: 20
Сложность: 290
Количество атомов изотопа: 0
Определенное количество стереоцентров атома: 0
Неопределенное количество стереоцентров атома: 0
Определенное количество стереоцентров связи: 0
Неопределенное количество стереоцентров связи: 0
Количество единиц ковалентной связи: 1
Соединение канонизировано: Да

Физическое состояние: жидкость
Цвет: бесцветный
Запах: слабый
Точка плавления/точка замерзания:
Температура плавления: -64 °С.
Начальная точка кипения и диапазон кипения: 327 °С – лит.
Горючесть (твердого тела, газа): Данные отсутствуют.
Верхний/нижний пределы воспламеняемости или взрывоопасности:
Верхний предел взрываемости: 3,2 %(В)
Нижний предел взрываемости: 0,8 %(В)
Температура вспышки: 109 °C – в закрытом тигле.
Температура самовоспламенения: 423 °C при 1,013 гПа.
Температура разложения: Данные отсутствуют.
pH: нейтральный

Вязкость:
Вязкость, кинематическая: 13,96 мм2/с при 40 °C
Вязкость, динамическая: данные отсутствуют.
Растворимость в воде 0,02 г/л при 20 °C - слабо растворим.
Коэффициент распределения: н-октанол/вода:
log Pow: 4,11 при 20 °C
Давление пара: 0,11 гПа при 100 °C.
Плотность: 1039 г/см3 при 25 °C – лит.
Относительная плотность: данные отсутствуют.
Относительная плотность пара: данные отсутствуют.
Характеристики частиц: данные отсутствуют.
Взрывоопасные свойства: данные отсутствуют.
Окислительные свойства: нет
Другая информация по безопасности: данные отсутствуют.

Точка плавления: -64 °С.
Точка кипения: 295,3±8,0 °C при 760 мм рт.ст.
Температура вспышки: 153,9±7,9 °C.
Молекулярная формула: C16H22O4.
Молекулярный вес: 278,344
Плотность: 1,0±0,1 г/см3
Молекулярная формула: C16H22O4.
Название ИЮПАК: бис(2-метилпропил)бензол-1,2-дикарбоксилат.
Номер кассы: 84-69-5
Молекулярный вес: 278,34 г/моль.
Плотность: 1,039 г/мл
Точка кипения: 320 °С.
Температура вспышки: 185 °С.

Плотность: 1,043 г/мл при 25 °C (лит.)
Точка плавления: -35 °C (лит.)
Точка Болинга: 340 °C (лит.)
Температура вспышки: 340°F
Растворимость в воде: слабо растворим. 0,0013 г/100 мл
Растворимость: Растворим в воде (0,4 мг/мл при 20 °C), этаноле.
Хорошо растворим в эфире, ацетоне и B.
Давление паров: 1 мм рт. ст. (147 °C)
Плотность пара: 9,6 (по сравнению с воздухом)
Внешний вид: Бесцветная жидкость.
Удельный вес: 1,049 (20/20 ℃)
Цвет: APHA: ≤10
Предел воздействия NIOSH REL: TWA 5 мг/м3, IDLH 4000 мг/м3;
OSHA PEL: TWA5 мг/м3; ACGIH TLV: TWA 5 мг/м3.
Мерк: 14,3035
РН: 1914064

Тип соединения Palatinol IC:
Ароматический углеводород
Косметический токсин
Эстер
Эфир
Бытовой токсин
Промышленный/рабочий токсин
Метаболит
Органическое соединение
Фталат
Пластификатор
Синтетическое соединение

Альтернативные родители Palatinol IC:
Бензоильные производные
Дикарбоновые кислоты и производные
Эфиры карбоновых кислот
Кислородорганические соединения
Органические оксиды
Производные углеводородов

Заместители Palatinol IC:
Бензоатный эфир
Бензоил
Дикарбоновая кислота или производные
Эфир карбоновой кислоты
Производное карбоновой кислоты
Органическое кислородное соединение
Органический оксид
Производное углеводорода
Кислородорганическое соединение
Ароматическое гомомоноциклическое соединение
Palladium (II) Acetate
Palladium (II) Acetate; Palladium(II) acetate; Palladium diacetate; hexakis(acetato)tripalladium; bis(acetato)palladium cas no: 3375-31-3
PALM ACID
PALM ALCOHOL, N° CAS : 93762-75-5. Nom INCI : PALM ALCOHOL. N° EINECS/ELINCS : 297-792-5. Classification : Alcool. Ses fonctions (INCI). Agent d'entretien de la peau : Maintient la peau en bon état
PALM ALCOHOL
PALM KERNEL ACID, N° CAS : 101403-98-9, Nom INCI : PALM KERNEL ACID, N° EINECS/ELINCS : 309-936-7. Classification : Huile de Palme (Dérivé). Ses fonctions (INCI). Agent nettoyant : Aide à garder une surface propre. Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile)