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SODIUM CAPRYLATE
SODIUM CAPRYLOAMPHOACETATE, Nom INCI : SODIUM CAPRYLOAMPHOACETATE. Nom chimique : Octanamide, N-[2-[N-(2-hydroxyethyl)-N-(carboxymethyl)amino]ethyl]-, sodium salt Ses fonctions (INCI). Agent nettoyant : Aide à garder une surface propre. Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide. 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 Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM CAPRYLOAMPHOACETATE
SODIUM CARBOMER N° CAS : 73298-57-4 Nom INCI : SODIUM CARBOMER Classification : Polymère de synthèse Ses fonctions (INCI) Stabilisateur d'émulsion : Favorise le processus d'émulsification et améliore la stabilité et la durée de conservation de l'émulsion Agent filmogène : Produit un film continu sur la peau, les cheveux ou les ongles Gélifiant : Donne la consistance d'un gel à une préparation liquide Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques
SODIUM CARBOMER
SODIUM CARBOXYMETHYL STARCH, N° CAS : 9063-38-1 Nom INCI : SODIUM CARBOXYMETHYL STARCH Ses fonctions (INCI) Agent fixant : Permet la cohésion de différents ingrédients cosmétiques Stabilisateur d'émulsion : Favorise le processus d'émulsification et améliore la stabilité et la durée de conservation de l'émulsion Agent filmogène : Produit un film continu sur la peau, les cheveux ou les ongles Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques
SODIUM CARBONATE(HEAVY)
SODIUM CARBONATE(HEAVY) Sodium Carbonate(Heavy) is a strong alkali base used in green cleaning products. Often found in powder form, it's used in a wide range of industries, such as in cleaning and personal care products and as a fungicide, microbicide, herbicide, and pH adjuster. What Is Sodium Carbonate(Heavy)? Sodium Carbonate(Heavy) is a chemical compound with the molecular formula Na2CO3. It's commonly referred to as washing soda and is used in cleaning products, glass production, as a food additive, and more. Synonyms Sodium Carbonate(Heavy) may go by the following names: Washing soda Soda ash DiSodium Carbonate(Heavy) Calcined soda Carbonic acid disodium salt Solvay soda 497-19-8 Properties Sodium Carbonate(Heavy) is alkali with a high pH when in concentrated solutions. When it is added to water it breaks down into carbonic acid and sodium hydroxide (lye). Cleaning Uses Sodium Carbonate(Heavy) is used in several cleaning products, including green cleaning ones, due to its disinfectant properties and ability to cut through grease and soften water. You can find it in laundry detergents, automatic dishwashing detergents, all-purpose cleaners, glass cleaners, stain removers, countertop cleaners, sanitizing sprays, and bleach. To clean and disinfect with Sodium Carbonate(Heavy), the Environmental Protection Agency (EPA) recommends using 2 ounces per gallon of water.1 This solution can be used to clean hard, non-porous surfaces, such as floors, walls, bathtubs, tile, and grout. Sodium Carbonate(Heavy) is considered an irritant at concentrations below 15 percent and caustic above 15 percent according to the EPA, so keep this in mind when mixing your cleaning solutions with it.1 Wear cleaning gloves and avoid getting it in your eyes or mouth. Other Uses In addition to its use in cleaning products, Sodium Carbonate(Heavy) is used in: Chemical manufacturing Food (e.g., anticaking agent) Glass manufacturing Personal care products (e.g., bubble bath, toothpaste, bath salts and soaks, and scrubs) Pulp and paper products Swimming pool maintenance (to adjust the pH) Therapeutic treatments (e.g., to treat dermatitides) Veterinary medicine treatments (e.g., to treat ringworm, cleanse the skin, and treat eczema) Product Brands Containing Sodium Carbonate(Heavy) To see if certain products contain Sodium Carbonate(Heavy), try searching the U.S. Department of Health and Human Services Household Products Database, the Environmental Working Group's (EWG) Guide to Healthy Cleaning, the Good Guide, or the EWG's Skin Deep Cosmetic Database. If using the general term "Sodium Carbonate(Heavy)" doesn't generate a lot of results, try entering one of its synonyms. Regulation When Sodium Carbonate(Heavy) is used in personal care products, food, or drugs, it is monitored by the U.S. Food and Drug Administration (FDA). For other uses, such as pesticides and cleaning products, it is monitored by the EPA. Health and Safety The EPA considers Sodium Carbonate(Heavy) a safe pesticide and the FDA designates it as generally regarded as safe (GRAS). In the 2006 "Reregistration Eligibility Decision (R.E.D) for Sodium Carbonate(Heavy); Weak Mineral Bases," the EPA notes that there are no known human health hazards when Sodium Carbonate(Heavy) is used according to EPA and FDA GRAS guidelines and that "no additional information is needed" to assess its safety.1 After seeking immediate medical attention, here are some home care, first-aid guidelines: Ingestion: Have the person drink a glass of water or milk unless otherwise advised by a health care provider. However, do not have them drink if they are having any of the serious symptoms such as vomiting, convulsions, or drowsiness and have difficulty swallowing. Do not have the person vomit unless to told to do so by a doctor or poison control center. Eye or skin contact: Flush with plenty of water for a minimum of 15 minutes. Inhalation: Move the person to fresh air. Environmental Effects According to the 2006 R.E.D document, the EPA considers Sodium Carbonate(Heavy) to be a naturally occurring chemical found in soil and water and doesn't expect any adverse effects on wildlife or water if low amounts are released into the environment. Therefore, it could be considered green.1 Source Most of the world's supply of Sodium Carbonate(Heavy) is derived from processing trona ore, which is mined in southwest Wyoming.2 Making Sodium Carbonate(Heavy) Interestingly enough, you can also make Sodium Carbonate(Heavy) from baking soda by baking it in the oven. Sodium Carbonate(Heavy) Jump to navigationJump to search Not to be confused with Sodium bicarbonate (baking soda), a similar compound. Sodium Carbonate(Heavy) Skeletal formula of Sodium Carbonate(Heavy) Sample of Sodium Carbonate(Heavy) Names IUPAC name Sodium Carbonate(Heavy) Other names Soda ash, washing soda, soda crystals, sodium trioxocarbonate Identifiers CAS Number 497-19-8 (anhydrous) check 5968-11-6 (monohydrate) ☒ 6132-02-1 (decahydrate) ☒ 3D model (JSmol) Interactive image ChEBI CHEBI:29377 check ChEMBL ChEMBL186314 check ChemSpider 9916 check ECHA InfoCard 100.007.127 Edit this at Wikidata EC Number 207-838-8 E number E500(i) (acidity regulators, ...) PubChem CID 10340 RTECS number VZ4050000 UNII 45P3261C7T check CompTox Dashboard (EPA) DTXSID1029621 Edit this at Wikidata InChI[show] SMILES[show] Properties Chemical formula Na2CO3 Molar mass 105.9888 g/mol (anhydrous) 286.1416 g/mol (decahydrate) Appearance White solid, hygroscopic Odor Odorless Density 2.54 g/cm3 (25 °C, anhydrous) 1.92 g/cm3 (856 °C) 2.25 g/cm3 (monohydrate)[1] 1.51 g/cm3 (heptahydrate) 1.46 g/cm3 (decahydrate)[2] Melting point 851 °C (1,564 °F; 1,124 K) (Anhydrous) 100 °C (212 °F; 373 K) decomposes (monohydrate) 33.5 °C (92.3 °F; 306.6 K) decomposes (heptahydrate) 34 °C (93 °F; 307 K) (decahydrate)[2][6] Solubility in water Anhydrous, g/100 mL: 7 (0 °C) 16.4 (15 °C) 34.07 (27.8 °C) 48.69 (34.8 °C) 48.1 (41.9 °C) 45.62 (60 °C) 43.6 (100 °C)[3] Solubility Soluble in aq. alkalis,[3] glycerol Slightly soluble in aq. alcohol Insoluble in CS2, acetone, alkyl acetates, alcohol, benzonitrile, liquid ammonia[4] Solubility in glycerine 98.3 g/100 g (155 °C)[4] Solubility in ethanediol 3.46 g/100 g (20 °C)[5] Solubility in dimethylformamide 0.5 g/kg[5] Acidity (pKa) 10.33 Magnetic susceptibility (χ) −4.1·10−5 cm3/mol[2] Refractive index (nD) 1.485 (anhydrous) 1.420 (monohydrate)[6] 1.405 (decahydrate) Viscosity 3.4 cP (887 °C)[5] Structure Crystal structure Monoclinic (γ-form, β-form, δ-form, anhydrous)[7] Orthorhombic (monohydrate, heptahydrate)[1][8] Space group C2/m, No. 12 (γ-form, anhydrous, 170 K) C2/m, No. 12 (β-form, anhydrous, 628 K) P21/n, No. 14 (δ-form, anhydrous, 110 K)[7] Pca21, No. 29 (monohydrate)[1] Pbca, No. 61 (heptahydrate)[8] Point group 2/m (γ-form, β-form, δ-form, anhydrous)[7] mm2 (monohydrate)[1] 2/m 2/m 2/m (heptahydrate)[8] Lattice constant a = 8.920(7) Å, b = 5.245(5) Å, c = 6.050(5) Å (γ-form, anhydrous, 295 K)[7] α = 90°, β = 101.35(8)°, γ = 90° Coordination geometry Octahedral (Na+, anhydrous) Thermochemistry Heat capacity (C) 112.3 J/mol·K[2] Std molar entropy (So298) 135 J/mol·K[2] Std enthalpy of formation (ΔfH⦵298) −1130.7 kJ/mol[2][5] Gibbs free energy (ΔfG˚) −1044.4 kJ/mol[2] Hazards Main hazards Irritant Safety data sheet MSDS GHS pictograms GHS07: Harmful[9] GHS Signal word Warning GHS hazard statements H319[9] GHS precautionary statements P305+351+338[9] NFPA 704 (fire diamond) [11] NFPA 704 four-colored diamond 010 Lethal dose or concentration (LD, LC): LD50 (median dose) 4090 mg/kg (rat, oral)[10] Related compounds Other anions Sodium bicarbonate Other cations Lithium carbonate Potassium carbonate Rubidium carbonate Caesium carbonate Related compounds Sodium sesquicarbonate Sodium percarbonate Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ☒ verify (what is check☒ ?) Infobox references Sodium Carbonate(Heavy), Na2CO3, (also known as washing soda, soda ash and soda crystals) is the inorganic compound with the formula Na2CO3 and its various hydrates. All forms are white, water-soluble salts that yield moderately alkaline solutions in water. Historically it was extracted from the ashes of plants growing in sodium-rich soils. Because the ashes of these sodium-rich plants were noticeably different from ashes of wood (once used to produce potash), Sodium Carbonate(Heavy) became known as "soda ash."[12] It is produced in large quantities from sodium chloride and limestone by the Solvay process. Contents 1 Hydrates 1.1 Washing soda 2 Applications 2.1 Glass manufacture 2.2 Water softening 2.3 Food additive and cooking 2.4 Inexpensive, weak base 2.5 Precursor to other compounds 2.6 Miscellaneous 3 Physical properties 4 Occurrence as natural mineral 5 Production 5.1 Mining 5.2 Barilla and kelp 5.3 Leblanc process 5.4 Solvay process 5.5 Hou's process 6 See also 7 References 8 Further reading 9 External links Hydrates Sodium Carbonate(Heavy) is obtained as three hydrates and as the anhydrous salt: Sodium Carbonate(Heavy) decahydrate (natron), Na2CO3·10H2O, which readily effloresces to form the monohydrate. Sodium Carbonate(Heavy) heptahydrate (not known in mineral form), Na2CO3·7H2O. Sodium Carbonate(Heavy) monohydrate (thermonatrite), Na2CO3·H2O. Also known as crystal carbonate. anhydrous Sodium Carbonate(Heavy), also known as calcined soda, is formed by heating the hydrates. It is also formed when sodium hydrogen carbonate is heated (calcined) e.g. in the final step of the Solvay process. The decahydrate is formed from water solutions crystallizing in the temperature range -2.1 to +32.0 °C, the heptahydrate in the narrow range 32.0 to 35.4 °C and above this temperature the monohydrate forms.[13] In dry air the decahydrate and heptahydrate lose water to give the monohydrate. Other hydrates have been reported, e.g. with 2.5 units of water per Sodium Carbonate(Heavy) unit ("pentahemihydrate").[14] Washing soda Sodium Carbonate(Heavy) decahydrate (Na2CO3·10H2O), also known as washing soda, is the most common hydrate of Sodium Carbonate(Heavy) containing 10 molecules of water of crystallization. Soda ash is dissolved in water and crystallized to get washing soda. {\displaystyle {\ce {Na2CO3 + 10H2O -> Na2CO3.10H2O}}}{\displaystyle {\ce {Na2CO3 + 10H2O -> Na2CO3.10H2O}}} It is transparent crystalline solid. It is one of the few metal carbonates which are soluble in water. It is alkaline with a pH level of 11; it turns red litmus to blue. It has detergent properties or cleansing properties, because it can remove dirt and grease from dirty clothes, etc. It attacks dirt and grease to form water soluble products, which are then washed away on rinsing with water. Applications Some common applications of Sodium Carbonate(Heavy) (or washing soda) include: Sodium Carbonate(Heavy) (or washing soda) is used as a cleansing agent for domestic purposes like washing clothes. Sodium Carbonate(Heavy) is a component of many dry soap powders. It is used for removing temporary and permanent hardness of water.[15] (see water softening). It is used in the manufacture of glass, soap and paper. (see glass manufacture) It is used in the manufacture of sodium compounds like borax Glass manufacture Sodium Carbonate(Heavy) serves as a flux for silica, lowering the melting point of the mixture to something achievable without special materials. This "soda glass" is mildly water-soluble, so some calcium carbonate is added to the melt mixture to make the glass insoluble. Bottle and window glass (soda-lime glass) is made by melting such mixtures of Sodium Carbonate(Heavy), calcium carbonate, and silica sand (silicon dioxide (SiO2)). When these materials are heated, the carbonates release carbon dioxide. In this way, Sodium Carbonate(Heavy) is a source of sodium oxide. Soda-lime glass has been the most common form of glass for centuries.[16] Water softening Water Hardness in United States Hard water contains dissolved compounds, usually calcium or magnesium compounds. Sodium Carbonate(Heavy) is used for removing temporary and permanent hardness of water.[15] As Sodium Carbonate(Heavy) is water-soluble and magnesium carbonate and calcium carbonate are insoluble, so it is used to soften water by removing Mg2+ and Ca2+. These ions form insoluble solid precipitates upon treatment with carbonate ions: {\displaystyle {\ce {Ca^2+ + CO3^2- -> CaCO3}}}{\displaystyle {\ce {Ca^2+ + CO3^2- -> CaCO3}}} {\displaystyle {\ce {Ca^2+(aq) + Na2CO3(aq) -> CaCO3(s) + 2Na+(aq)}}}{\displaystyle {\ce {Ca^2+(aq) + Na2CO3(aq) -> CaCO3(s) + 2Na+(aq)}}} Similarly, {\displaystyle {\ce {Mg^2+(aq) + Na2CO3(aq) -> MgCO3(s) + 2Na+(aq)}}}{\displaystyle {\ce {Mg^2+(aq) + Na2CO3(aq) -> MgCO3(s) + 2Na+(aq)}}} The water is softened because it no longer contains dissolved calcium ions and magnesium ions.[15] Food additive and cooking Sodium Carbonate(Heavy) is a food additive (E500) used as an acidity regulator, anticaking agent, raising agent, and stabilizer. It is one of the components of kansui (かん水), a solution of alkaline salts used to give ramen noodles their characteristic flavor and texture. It is used in the production of snus to stabilize the pH of the final product. Sodium Carbonate(Heavy) is used in the production of sherbet powder. The cooling and fizzing sensation results from the endothermic reaction between Sodium Carbonate(Heavy) and a weak acid, commonly citric acid, releasing carbon dioxide gas, which occurs when the sherbet is moistened by saliva. In China, it is used to replace lye-water in the crust of traditional Cantonese moon cakes, and in many other Chinese steamed buns and noodles. In cooking, it is sometimes used in place of sodium hydroxide for lyeing, especially with German pretzels and lye rolls. These dishes are treated with a solution of an alkaline substance to change the pH of the surface of the food and improve browning. Sodium Carbonate(Heavy) is corrosive to aluminum cookware, utensils and foil. [17] Inexpensive, weak base Sodium Carbonate(Heavy) is also used as a relatively strong base in various fields. As a common alkali, it is preferred in many chemical processes because it is cheaper than NaOH and far safer to handle. Its mildness especially recommends its use in domestic applications. For example, it is used as a pH regulator to maintain stable alkaline conditions necessary for the action of the majority of photographic film developing agents. It is also a common additive in swimming pools and aquarium water to maintain a desired pH and carbonate hardness (KH). In dyeing with fiber-reactive dyes, Sodium Carbonate(Heavy) (often under a name such as soda ash fixative or soda ash activator) is used to ensure proper chemical bonding of the dye with cellulose (plant) fibers, typically before dyeing (for tie dyes), mixed with the dye (for dye painting), or after dyeing (for immersion dyeing). It is also used in the froth flotation process to maintain a favourable pH as a float conditioner besides CaO and other mildly basic compounds. Precursor to other compounds Sodium bicarbonate (NaHCO3) or baking soda, also a component in fire extinguishers, is often generated from Sodium Carbonate(Heavy). Although NaHCO3 is itself an intermediate product of the Solvay process, the heating needed to remove the ammonia that contaminates it decomposes some NaHCO3, making it more economic to react finished Na2CO3 with CO2: Na2CO3 + CO2 + H2O → 2NaHCO3 In a related reaction, Sodium Carbonate(Heavy) is used to make sodium bisulfite (NaHSO3), which is used for the "sulfite" method of separating lignin from cellulose. This reaction is exploited for removing sulfur dioxide from flue gases in power stations: Na2CO3 + SO2 + H2O → NaHCO3 + NaHSO3 This application has become more common, especially where stations have to meet stringent emission controls. Sodium Carbonate(Heavy) is used by the cotton industry to neutralize the sulfuric acid needed for acid delinting of fuzzy cottonseed. Miscellaneous Sodium Carbonate(Heavy) is used by the brick industry as a wetting agent to reduce the amount of water needed to extrude the clay. In casting, it is referred to as "bonding agent" and is used to allow wet alginate to adhere to gelled alginate. Sodium Carbonate(Heavy) is used in toothpastes, where it acts as a foaming agent and an abrasive, and to temporarily increase mouth pH. Sodium Carbonate(Heavy) is also used in the processing and tanning of animal hides.[citation needed] Physical properties The integral enthalpy of solution of Sodium Carbonate(Heavy) is −28.1 kJ/mol for a 10% w/w aqueous solution.[18] The Mohs hardness of Sodium Carbonate(Heavy) monohydrate is 1.3.[6] Occurrence as natural mineral Structure of monohydrate at 346 K. Sodium Carbonate(Heavy) is soluble in water, and can occur naturally in arid regions, especially in mineral deposits (evaporites) formed when seasonal lakes evaporate. Deposits of the mineral natron have been mined from dry lake bottoms in Egypt since ancient times, when natron was used in the preparation of mummies and in the early manufacture of glass. The anhydrous mineral form of Sodium Carbonate(Heavy) is quite rare and called natrite. Sodium Carbonate(Heavy) also erupts from Ol Doinyo Lengai, Tanzania's unique volcano, and it is presumed to have erupted from other volcanoes in the past, but due to these minerals' instability at the earth's surface, are likely to be eroded. All three mineralogical forms of Sodium Carbonate(Heavy), as well as trona, trisodium hydrogendicarbonate dihydrate, are also known from ultra-alkaline pegmatitic rocks, that occur for example in the Kola Peninsula in Russia. Extraterrestrially, known Sodium Carbonate(Heavy) is rare. Deposits have been identified as the source of bright spots on Ceres, interior material that has been brought to the surface.[19] While there are carbonates on Mars, and these are expected to include Sodium Carbonate(Heavy),[20] deposits have yet to be confirmed, this absence is explained by some as being due to a global dominance of low pH in previously aqueous Martian soil.[21] Production Mining Trona, trisodium hydrogendicarbonate dihydrate (Na3HCO3CO3·2H2O), is mined in several areas of the US and provides nearly all the domestic consumption of Sodium Carbonate(Heavy). Large natural deposits found in 1938, such as the one near Green River, Wyoming, have made mining more economical than industrial production in North America. There are important reserves of trona in Turkey; two million tons of soda ash have been extracted from the reserves near Ankara. It is also mined from some alkaline lakes such as Lake Magadi in Kenya by dredging. Hot saline springs continuously replenish salt in the lake so that, provided the rate of dredging is no greater than the replenishment rate, the source is fully sustainable.[citation needed] Barilla and kelp Several "halophyte" (salt-tolerant) plant species and seaweed species can be processed to yield an impure form of Sodium Carbonate(Heavy), and these sources predominated in Europe and elsewhere until the early 19th century. The land plants (typically glassworts or saltworts) or the seaweed (typically Fucus species) were harvested, dried, and burned. The ashes were then "lixiviated" (washed with water) to form an alkali solution. This solution was boiled dry to create the final product, which was termed "soda ash"; this very old name refers derives from the Arabic word soda, in turn applied to salsola soda, one of the many species of seashore plants harvested for production. "Barilla" is a commercial term applied to an impure form of potash obtained from coastal plants or kelp.[22] The Sodium Carbonate(Heavy) concentration in soda ash varied very widely, from 2–3 percent for the seaweed-derived form ("kelp"), to 30 percent for the best barilla produced from saltwort plants in Spain. Plant and seaweed sources for soda ash, and also for the related alkali "potash", became increasingly inadequate by the end of the 18th century, and the search for commercially viable routes to synthesizing soda ash from salt and other chemicals intensified.[23] Leblanc process Main article: Leblanc process In 1792, the French chemist Nicolas Leblanc patented a process for producing Sodium Carbonate(Heavy) from salt, sulfuric acid, limestone, and coal. In the first step, sodium chloride is treated with sulfuric acid in the Mannheim process. This reaction produces sodium sulfate (salt cake) and hydrogen chloride: 2NaCl + H2SO4 → Na2SO4 + 2HCl The salt cake and crushed limestone (calcium carbonate) was reduced by heating with coal.[16] This conversion entails two parts. First is the carbothermic reaction whereby the coal, a source of carbon, reduces the sulfate to sulfide: Na2SO4 + 2C → Na2S + 2CO2 The second stage is the reaction to produce Sodium Carbonate(Heavy) and calcium sulfide: Na2S + CaCO3 → Na2CO3 + CaS This mixture is called black ash. The soda ash is extracted from the black ash with water. Evaporation of this extract yields solid Sodium Carbonate(Heavy). This extraction process was termed lixiviation. The hydrochloric acid produced by the Leblanc process was a major source of air pollution, and the calcium sulfide byproduct also presented waste disposal issues. However, it remained the major production method for Sodium Carbonate(Heavy) until the late 1880s.[23][24] Solvay process Main article: Solvay process In 1861, the Belgian industrial chemist Ernest Solvay developed a method to make Sodium Carbonate(Heavy) by first reacting sodium chloride, ammonia, water, and carbon dioxide to generate sodium bicarbonate and ammonium chloride:[16] NaCl + NH3 + CO2 + H2O → NaHCO3 + NH4Cl The resulting sodium bicarbonate was then converted to Sodium Carbonate(Heavy) by heating it, releasing water and carbon dioxide: 2NaHCO3 → Na2CO3 + H2O + CO2 Meanwhile, the ammonia was regenerated from the ammonium chloride byproduct by treating it with the lime (calcium oxide) left over from carbon dioxide generation: 2NH4Cl + CaO → 2NH3 + CaCl2 + H2O The Solvay process recycles its ammonia. It consumes only brine and limestone, and calcium chloride is its only waste product. The process is substantially more economical than the Leblanc process, which generates two waste products, calcium sulfide and hydrogen chloride. The Solvay process quickly came to dominate Sodium Carbonate(Heavy) production worldwide. By 1900, 90% of Sodium Carbonate(Heavy) was produced by the Solvay process, and the last Leblanc process plant closed in the early 1920s.[16] The second step of the Solvay process, heating sodium bicarbonate, is used on a small scale by home cooks and in restaurants to make Sodium Carbonate(Heavy) for culinary purposes (including pretzels and alkali noodles). The method is appealing to such users because sodium bicarbonate is widely sold as baking soda, and the temperatures required (250 °F (121 °C) to 300 °F (149 °C)) to convert baking soda to Sodium Carbonate(Heavy) are readily achieved in conventional kitchen ovens.[25] Hou's process This process was developed by Chinese chemist Hou Debang in the 1930s. The earlier steam reforming byproduct carbon dioxide was pumped through a saturated solution of sodium chloride and ammonia to produce sodium bicarbonate by these reactions: CH4 + 2H2O → CO2 + 4H2 3H2 + N2 → 2NH3 NH3 + CO2 + H2O → NH4HCO3 NH4HCO3 + NaCl → NH4Cl + NaHCO3 The sodium bicarbonate was collected as a precipitate due to its low solubility and then heated up to approximately 80 °C (176 °F) or 95 °C (203 °F) to yield pure Sodium Carbonate(Heavy) similar to last step of the Solvay process. More sodium chloride is added to the remaining solution of ammonium and sodium chlorides; also, more ammonia is pumped at 30-40 °C to this solution. The solution temperature is then lowered to below 10 °C. Solubility of ammonium chloride is higher than that of sodium chloride at 30 °C and lower at 10 °C. Due to this temperature-dependent solubility difference and the common-ion effect, ammonium chloride is precipitated in a sodium chloride solution. The Chinese name of Hou's process, lianhe zhijian fa (联合制碱法), means "coupled manufacturing alkali method": Hou's process is coupled to the Haber process and offers better atom economy by eliminating the production of calcium chloride, since ammonia no longer needs to be regenerated. The byproduct ammonium chloride can be sold as a fertilizer. See also Natron Residual Sodium Carbonate(Heavy) index Sodium bicarbonate
SODIUM CARBOXYMETHYL STARCH
SODIUM CASEINATE, N° CAS : 9005-46-3, Nom INCI : SODIUM CASEINATE. Ses fonctions (INCI) : Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Agent d'entretien de la peau : Maintient la peau en bon état
SODIUM CASEINATE
sodium,heptadecyl sulfate; Hexadecylsulfuric Acid; Sodium Salt SODIUM CETYL STEARYL SULFATE cas no: 59186-41-3
SODIUM CASEINATE
CAS number: 9005-46-3
EC number: 618-419-8

Sodium caseinate is a compound derived from casein, a protein present in the milk of mammals.
Casein is the dominant protein in cow’s milk and responsible for its opaque, white appearance.
sodium caseinate’s an integral component of many milk-based products like ice cream and cheese.
Casein proteins can be separated from milk and used independently as a supplement or additive to thicken, texturize, and stabilize various food products.
Sodium caseinate can be used as a protein supplement and to alter the texture and stability of various products, such as baked goods, cheeses, ice cream, medications, and soap.

How sodium caseinate’s made
The terms casein and sodium caseinate are often used interchangeably, but they differ slightly on a chemical level.
Sodium caseinate is a compound that forms when casein proteins are chemically extracted from skim milk.

First, the solid casein-containing curds are separated from the whey, which is the liquid part of milk.
This can be done by adding specialized enzymes or an acidic substance — like lemon juice or vinegar — to the milk.
Once the curds have been separated from the whey, they’re treated with a basic substance called sodium hydroxide before being dried into a powder.

The resulting sodium caseinate powder can then be used in a variety of foods, including:
-protein powder
-coffee creamer
-cheese
-ice cream
-cheese-flavored snacks
-margarine
-cereal bars
-processed meats
-chocolate
-bread

What is Sodium Caseinate?
Sodium caseinates primary purpose is as an emulsifier.
The emulsification of sodium casein is mainly contributed to casein.
This is because casein is a protein, the molecules of that have both hydrophilic and hydrophobic groups, which can be attracted to water and fatty substances to achieve emulsification.

What is Sodium caseinate Made of?
Sodium casein is composed of protein, fat, calcium, sodium, lactose and others.

How is Sodium Caseinate made?
Like calcium caseinate, Sodium caseinate is produced by treating casein curd with an alkaline substance, here it is sodium hydroxide.
The insoluble casein is converted into a soluble form in this way.

How to Produce Casein?
Generally, casein is made from skim milk by two methods, precipitation by acid or coagulation by rennet, one is acid casein, another is rennet casein.

Applications:
-Cream liqueurs
-Nutritional beverages
-Processed cheese and spreads
-Soups
-Whipping agent
-Non-dairy creamer
-Processed meat

Description of Sodium caseinate:
Sodium caseinate is a kind of water soluble emulsifier.
Sodium caseinate has the function of stabilizing, strengthening protein, thickening, foaming etc.
Sodium caseinate is also a protein nutrition fortifier.
Sodium caseinate has also been used in bread, biscuits, and other cereals.
Like casein, sodium caseinate is a high quality protein source.

Sodium caseinate is made from milk protein and is hydrolyzed and absorbed to participate in the normal metabolism of the body.
There is no definite chemical structure for sodium caseinate.
In electrophoretic analysis, there are at least 20 different kinds of protein components.
The main components are a mixture of alpha casein, beta casein and kappa casein (rather than simple proteins).

Sodium Caseinate can be used in Food, Beverage, Pharmaceutical, Health & Personal care products, Agriculture/Animal Feed/Poultry.
Sodium Caseinate is used as food emulsifier and thickening agent in bread, biscuits, candy, cakes, ice cream, yogurt drinks, and margarine, gravy, fast food, meat and seafood products.
Sodium caseinate is the biochemical name for casein, which is a type of protein found in the milk from all mammals.
Casein, which is Latin for “cheese,” is a major component of commercial cheese and its principle source of protein.
Some people are allergic to sodium caseinate, and it has been linked to some human diseases, mainly autism and gastrointestinal problems.

Sodium caseinate is a compound derived from casein, the main protein in milk.
sodium caseinate’s commonly used as a food additive because of its diverse nutritional and functional properties.
sodium caseinate’s used in nutrition supplements and processed foods like cheese, ice cream, bread, and cured meats, as well as in various cosmetic and personal care products.

Sodium caseinate, the sodium salt of casein (a milk protein), is a multi-functional food additive, and together with calcium caseinate, they’re dairy protein commonly used as an emulsifier, thickener or stabilizer in food.
Sodium caseinate improves the properties of food during processing and storage, as well as provides nutrition, taste and smell.

The following are the simple manufacturing process:
1. Acid Casein
The fresh milk, after the process of skimmed and pasteurized, then add acid (lactic acid, acetic acid, hydrochloric acid or sulfuric acid) and adjust the pH to 4.6 to make the casein micelles lose their charge and solidify & precipitate. Then followed by neutralization and drying.

2. Rennet Casein
Made from skim milk, then add rennetase to form a coagulated precipitate.

This ingredient has the following features:
-Good emulsifying properties
-Good water solubility
-Good whipping properties
-Low flavour profile
-Good nutritional value
-Good retort stabilty

This ingredient can be used in the following applications:
-Whipped toppings
-Coffee whiteners
-Cream liqueurs
-Nutritional products
-Wet blend ingredient for susceptible population
-Not intended for use as a Dry Blend ingredient for infants
Synergy
Sodium caseinate itself is a high molecular weight protein that has a certain viscosity in an aqueous solution.
The combined uses with some thickeners, such as carrageenan, guar gum, and CMC can greatly improve its thickening and suspension stability.
The synergistic effect with carrageenan is the best, in addition to increasing the viscosity, it can also improve the emulsifying ability.

Heat Stable
Sodium caseinates emulsion can be sterilized at 120 ℃ for a long time without destroying its stability and functionality.

What’re the applications of Sodium Caseinate?
With Sodium caseinates emulsification, foaming, thickening, hydration, gelling and other properties, plus it is a protein, sodium caseinate is widely used in food, cosmetics and pharmaceutical industries.

Food
Sodium caseinates uses of food grade are more wider than casein due to the water-soluble property.
The common applications are in ice cream, meat products, bread, cereal products and etc.
Let’s see Sodium caseinates functions and suggested uses in food categories.

Sausage
Sodium caseinate can make fat distribution evenly, enhance the stickiness of the meat.
The common usage: 0.2-0.5%.

Ice cream
Ice cream contains a certain amount of fat and non-fat milk solids.
The common usage of sodium caseinate is 0.2-0.3%.
Sodium caseinate is added as/to:

There are several types of caseinates, but sodium caseinate is usually preferred because it’s the most water-soluble, meaning that it readily mixes with other substances.
Sodium caseinate is a food additive and nutritional supplement derived from the milk protein casein.

A variety of uses
Sodium caseinate is an ingredient with many broad and useful applications in the food, cosmetic, and personal care industries.

Nutrition supplements
Casein comprises approximately 80% of the protein in cow’s milk, while whey accounts for the remaining 20%.
Sodium caseinate is a popular protein choice in supplements like protein powders, snack bars, and meal replacements because it provides a rich source of high quality and complete protein.

Proteins are considered complete if they contain all nine essential amino acids that your body needs to stay healthy.
Research suggests that casein can promote the growth and repair of muscle tissue, which makes it a popular protein supplement choice among athletes and weight lifters.
Due to Sodium caseinates favorable amino acid profile, sodium caseinate is also frequently used as a protein source in infant formulas.

Food additive
In addition to being a great source of protein, sodium caseinate has many functional attributes that make it a popular additive in the food industry.
For example, sodium caseinate has a high capacity for water absorption, meaning it can be used to modify the texture of foods like dough and commercially prepared baked goods .
sodium caseinate’s also frequently used as an emulsifier to keep fats and oils suspended in products like processed and cured meats.
Sodium caseinate’s unique melting properties also make it useful for producing natural and processed cheeses, while its foaming properties make it an ideal additive in products like whipped toppings and ice cream.

Other applications
Although sodium caseinate’s usually added to food, sodium caseinate is also used to change the texture and chemical stability of a variety of other products like pharmaceutical drugs, soap, makeup, and personal care products.

An emulsifying stabilizer, which can avoid the shrinking and deforming caused by the low milk solids content.
Reduce lactose content in the formulation, prevent lactose from crystallizing during freezing and storage of the finished product.

Bakery
Sodium caseinate combines with gluten protein to improve the stability and gas retention of the gluten network, enhance the dough’s elasticity and toughness.
In addition, sodium caseinate can also interact with amylose, thereby soften and extend the shelf life of bread.

Coffee Mate
Sodium caseinate is the main ingredient of coffee mate or non-dairy cream due to its three characteristics:

With a high protein content.
A strong emulsifying effect with fat and it can prevent the agglomeration and accumulation of fat.
Increasing the viscosity and mouthfeel of coffee mate, making the product taste more delicious.

Food supplement
Due to Sodium caseinates high protein content, Sodium caseinate can be combined with cereal products to produce high-protein cereal products, elderly foods, infant foods and diabetic foods.
In addition, sodium caseinate can also be added to dairy products such as margarine, chocolate, whipped toppings, desserts, and cheese as an emulsifier and foaming agent to increase the viscosity of the aqueous phase, stabilize the emulsification system, increase the viscosity of bubbles, and prevent fat balls.

Cosmetics
Per the “European Commission database for information on cosmetic substances and ingredients”, sodium caseinate acts as an antistatic, hair conditioning, and skin conditioning agent in cosmetic and personal care products.

CHARACTERISTIC of Sodium caseinate:
White to yellowish colour, free flowing powder, typical milk taste and smell without foreign odour.

APPLICATIONS of Sodium caseinate:
Food supplements (baby food and sports nutrition), coffee creamers, drinks and dietetic products, meat industry, processed and hard cheese.

BENEFITS of Sodium caseinate:
Improvement of nutrition features, high emulsification, gelling properties (good viscosity), enrich products with organic amino-acids, foaming capability, water and fat absorbability.

Casein has a wide variety of uses, from being a major component of cheese, to use as a food additive.
The most common form of casein is sodium caseinate.
In milk, casein undergoes phase separation to form colloidal casein micelles, a type of secreted biomolecular condensate.
These highly purified caseinate proteins have a good nutritional value and excellent functional properties (emulsion, thickening).

Dietetics :
- Clinical nutrition
- Slimming and nutritional foods

Food industries :
- Meat processing
- Meat, ready-cooked dishes
- Dairy products
- Coffee whiteners

The enzyme trypsin can hydrolyze off a phosphorus-containing peptone.
The commercial product also known as casein is used in adhesives, binders, protective coatings, and other products.
The purified material is a water-insoluble white powder.
While Sodium caseinate is also insoluble in neutral salt solutions, Sodium caseinate is readily dispersible in dilute alkalies and in salt solutions such as those of sodium oxalate and sodium acetate.

Definition of Sodium caseinate:
Though commonly regarded as the principal protein in milk (approximately 3%), casein is actually a colloidal aggregate composed of several identifiable proteins together with phosphorus and calcium.
Sodium caseinate occurs in milk as a heterogeneous complex called calcium caseinate, which can be fractionated by a number of methods.
Sodium caseinate can be precipitated with acid at p H 4.7 or with the enzyme rennet (rennin).
The product of the latter method is called paracasein, the term being applied to any of the casein fractions involved, i.e., α, β, κ, etc.
Sodium Caseinates are protein products mainly used in the food-, sports- and diet- industries because of their various functional properties.

Product information
Sodium caseinates are produced from fresh skimmed milk.
With Neutralization the curds from the skim milk acid coagulation are made soluble.
After that, the protein contained in the curd is rendered functional and soluble.
Finally an alkali containing sodium (sodium hydroxide or soda) is added.
After that the dehydration (drying) is the last step.

Spray dried Sodium caseinates are known for their highly viscosity and emulsifying properties.
That’s why they are often applied in ready meals, sausages, coffee creamers and other dairy products.

Extruded sodium caseinates are neutralized in an extruder.
The dry matter of the final product is close to 94%.
In the next step the extruded sodium caseinates are grounded.
This allows to get a desired particle size. The product is often applied in coffee creamer and delicatessen.

Applications of Sodium caseinate:
-Ready-to-eat-meals
-Dairy products
-Dietetics
-Meat processing (for example sausages)
-Sports nutrition
-Coffee whiteners
-Product’s advantages

Sodium caseinate has Emulsifier and thickening qualities
Sodium caseinate has Texturizing properties
Sodium caseinate has a low viscosity

Sodium caseinate is made from casein which is the main protein present in milk which is used as an excellent food additive and for industrial purposes as it contains high protein & nutritional value.
In food industry Sodium caseinate is used to improve the quality of products.
Sodium caseinate is totally safe for consumption as it is announced as unrestricted food additive by FAO and WHO, so, used in all kinds of food products such as meat products, roasted food, artificial cream, coffee partner, baby food, cheese, various cake and candies, beverages, medicine for daily uses and many more.

Useful in a wide variety of applications, our Sodium Caseinate provides excellent functionality, helping to deliver texture in your products and provides whitening and a clean, milky flavour to beverages.
A spray dried protein powder made from premium quality acid casein.
Adds texture to your products by thickening and stabilising; adds thickness and opacity to sauces.

Highly functional for creamers, providing opacity and helping enhance foam structure.
Has a bland milky flavour making Sodium caseinate ideal for use in flavour sensitive formulations and high protein beverages.

Applications:
-Bakery
-Yogurt & ice cream
-Confectionery & chocolate
-Beverages

Chemical Properties
White to cream colored powder

Uses:
Sodium Caseinate is the sodium salt of casein, a milk protein.
Sodium caseinate is used as a protein source and for its functional properties such as water binding, emulsification, whitening, and whipping.
Sodium caseinate is used in coffee whiteners, nondairy whipped toppings, processed meat, and desserts.
Casein is the phosphoprotein of fresh milk; the rennin-coagulated product is sometimes called paracasein.
British nomenclature terms the casein of fresh milk caseinogen and the coagulated product casein.

As Sodium caseinate exists in milk it is probably a salt of calcium.
Casein is not coagulated by heat.
Sodium caseinate is precipitated by acids and by rennin, a proteolytic enzyme obtained from the stomach of calves. Casein is a conjugated protein belonging to the group of phosphoproteins.

Sodium caseinate is obtained from casein, a protein found in mammal's milk.
Sodium caseinate is rich in protein and is usually used as a protein supplement and food additive.

Uses Of Sodium Caseinate
-Protein supplement - This sodium caseinate powder can be used as a protein powder because it provides a rich source of high quality protein.
Sodium caseinate contains 90 per cent protein.
This essential nutrient is required for the body for building and repairing muscle tissues, improving bone health and boosting metabolism.
As sodium caseinate is high in protein, it would make an excellent protein supplement choice among athletes and people involved in strength training .

-Food additive - In the food industry, sodium caseinate is used as a food additive.
Sodium caseinate can be used to change the texture and stabilise many kinds of food products such as ice cream, cheese, coffee creamer, cereal bars, chocolate, bread, margarine, cheese-flavoured snacks and processed meats.

What Is Sodium Caseinate And How Its Made?
Milk is curdled by adding specialised enzymes or an acidic substance such as lemon juice or vinegar to it.
After which, the solid curds are separated from the whey, which is the liquid part of the milk.
Once the curd has been separated, they are treated with an alkali called sodium hydroxide, and are then dried and formed into a powder.

Sodium caseinate is called sodium caseinate, which is extracted from casein and contains 90 per cent protein.
Casein and sodium caseinate are almost the same products and can be used in the same manner, but they vary on a chemical level.
A high quality milk protein product, manufactured from fresh pasteurised skimmed milk through acid precipitation of the casein followed by neutralisation and drying.

Sodium Caseinate uses as follows:
In Food
Sodium Caseinate can be used as nutritional suppliments, thickener, emulsifier and texture stabilizer in food such as in bread, biscuits, candy, cakes, ice cream, yogurt drinks, and margarine, gravy, fast food, meat and seafood products.
In sausage, Sodium caseinate can be used to make fat distribution uniform, and enhance the adhesion property of meat. The dosage in sausage is 0.2%-0.3%.
In the fish cake, Sodium caseinate can improve the elasticity.

In ice cream, the use of sodium caseinate helps to the bubble of products stable and to prevent sugar condensation and contraction.
In bread Sodium caseinate is used to achieve enhancement.
In bread, biscuit and noodles, the dosage is 0.2%-0.5%; in foreign pastry, doughnut and chocolate, Sodium caseinate is 0.59%-5.0% while in cream milk beverages, it is 0.2%-0.39%.
In addition, gellan gum can also be used in dairy products and egg products.

In Beverage
Sodium Caseinate can be used as nutritional suppliments, thickener, emulsifier and texture stabilizer in beverage.

In Pharmaceutical
Sodium Caseinate can be used as intermediate in Pharmaceutical.

In Health and Personal care
Sodium Caseinate can be used in cosmetic and personal care products.

CHEMICAL PARAMETERS:
Protein (as is %): ≥ 87,0 (92,5% in dry matter)
Fat (%): ≤ 2,0
Moisture (%): ≤ 6,0
Ash (%): ≤ 4,5
pH: ≤ 7,0
Insolubility (ml): ≤ 1,0
Lactose (%): ≥ 0,5
Purity (disc): A, A/B

MICROBIOLOGICAL PARAMETERS:
Total Plate Count /g: ≤2 000
Coliforms/0,1g: absent
E- Coli /0,1 g: absent
Salmonella /25 g: absent
Antibiotics: absent
Yeast /g: ≤ 50
Mould /g: ≤ 50

SYNONYMS:
CASEIN SODIUM
CASEIN SODIUM MILK
CASEIN SODIUM SALT
casein,sodiumcomplex
Caseins,sodiumcomplexes
sodiumcasein
luodanbaisuanna
ldbsn
sodiumcomplex
NUTROSE
SODIUM CASEINATE
SODIUM CASEINATE FOOD GRADE
CASEIN FROM BOVINE MILK SODIUM
CaseinHydrolysate(Technical)(AcidHydrolysed)
Sodium caseinate, pract.
casein sodium salt from bovine milk
Casein Sodium from Milk
Casein Na salt
Casein SodiuM
Nutrose 〔Casein Sodium〕
Sodium caseite
Sodium Caseinate,>90%
Sodium caseinate USP/BP/EP
Sodium cascinate
SODIUM CETEARYL SULFATE
Sulfuric acid, C16-18-alkyl esters, sodium salts; SODIUM CETEARYL SULFATE, N° CAS : 59186-41-3. Origine(s) : Végétale, Synthétique. Nom INCI : SODIUM CETEARYL SULFATE. Classification : Sulfate, Tensioactif anionique. Ses fonctions (INCI): Agent nettoyant : Aide à garder une surface propre. Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide.Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM CETYL SULFATE
cas no 7775-09-9 Soda Chlorate; Chloric acid, sodium salt; chlorax; Chlorsaure (German); Natrium Chloraat (Dutch); Natrium Chlorat (German); Sodio (Clorato Di) (Italian); Sodium (Chlorate De) (French); Chlorate of Soda;
SODIUM CHLORATE
cas no 7758-19-2 Chlorous Acid, Sodium Salt; Chlorite (sodium salt); Natriumchlorit (German); Clorito de sodio (Spanish); Chlorite de sodium (French);
SODIUM CHLORIDE PHARMA
SODIUM CHLORIDE PHARMA What is it? Sodium chloride Pharma (NaCl) is the chemical name for salt. Sodium chloride Pharma occurs naturally as the mineral halite. Commercially, it is obtained by the solar evaporation of salt water, or by mining. It is a component of Sodium chloride Pharma injections USP, and has production uses in pharmaceutical processing.[1] Sodium chloride Pharma has uses a channeling agent, and as an osmotic agent in the cores of controlled-release tablets. It also is used to help modify drug release, and to adjust porosity in tablet coatings. It can adjust drug release from gels and emulsions, and adjust the thickness of solutions by altering the ionic attributes of a formulation.[1] Sodium chloride Pharma is widely used in a variety of pharmaceutical products to produce isotonic solutions. It is used in normal nasal saline sprays, in intravenous lock flush solutions, and in eye washes or solutions. Sodium chloride Pharma tablets are also available to replace salt lost through excess sweating to help prevent muscle cramps. Sodium chloride Pharma solution may also be used to dilute medications for nebulization and inhalation.[2] As an excipient, Sodium chloride Pharma may be regarded as nontoxic and nonirritant. However, toxic effects following the oral ingestion of 0.5–1.0 g per kilogram of body weight in adults may occur.[1] Abstract Sodium chloride Pharma ceutical applications must fulfill high purity requirements, as excipients or active pharmaceutical ingredients (API). In addition to the chemical purity, bacteriological limits must also be observed. The requirements are defined in pharmacopoeias (BP, Ch.P., JP, Ph.Eur., USP, KP, Ph.Rus.) and individually specified in quality agreements between salt producers and pharmaceutical companies. Solar salts and rock salts cannot be used directly as pharmaceutical salt due to their insufficient purity and/or increased microbial content. The required purity can only be achieved by crystallizing vacuum salt. For this purpose, the methods single effect, multiple effect, MVR and recrystallization are available. The first three technologies require additionally the removal of mother liquor from the crystals by washing with purified water, usually per production campaign. The recrystallization process doesn’t require additional washing due to the low sulfate concentration in the process brine loop. The sulfate requirements for pharmaceutical salt will be automatically fulfilled. Generally, high bromide and potassium contents in the crude salt or in the crude brine make the production of pharmaceutical salt difficult or even impossible. Several case studies from Europe, Asia and Africa confirm the recrystallization process as suitable for the production of pharmaceutical salt. The production of API Sodium chloride Pharma requires compliance with GMP standards (FDA, EU-GMP). Pharmaceutical salt with extreme low sulfate limits, like in China, needs additional sulfate removal from the raw brine and/or double crystallization. Since anticaking agents or free-flow additives may not be used for pharmaceutical salt, special measures are required to prevent caking of the salt. Granulation can be an additional process step. One possible application for granulation is the production of dry dialysis concentrates, where only the pharmaceutical grade vacuum salt is granulated or in mixture with other salts required for the dialysis. The preparation of pharmaceutical grade brine requires removal of undesirable ions, such as calcium, magnesium, and sulfate. This can be achieved by chemical precipitation, ion exchange and/or nanofiltration. The main applications of pharmaceutical sodium chloride are hemodialysis and peritoneal dialysis. Further applications include IV (intravenous) solutions, oral rehydration salts and extraction of biological heparin. Due to the worldwide growing demand, this market segment might be of increasing interest for salt producers. Pharmaceutical grade sodium chloride is required for dialysis solutions (hemodialysis, peritoneal dialysis, hemofiltration), intravenous (IV) injections, oral rehydration salts, channeling agents, osmotic agents, cleansing solutions, pharmaceutical formulations, nutrition (enteral, parenteral), extraction of biological heparin, and non-medical applications (corrosion testing, cosmetics, etc.). Dialysis application dominates with a 50% share the global market due to the worldwide mounting kidney failure. The worldwide increasing wealth also drives the pharmaceutical grade Sodium chloride Pharma market as spending in the healthcare sector are increasing. Dialysis is used as replacement for lost kidney functions, cleaning the blood from waste products through artificial means. Renal dialysis is vital to a growing number of patients around the world and the only alternative for many people, because kidney transplantation is precluded due to a shortage of donor organs. Sodium chloride is the major component of dry and liquid hemodialysis concentrates, as well as peritoneal dialysis solutions. The second key application of pharmaceutical grade Sodium chloride Pharma are IV solutions. These solutions have a wide range of applications which include regulation of blood pressure, hydration, electrolyte balance, medication and nutrition delivery, flushing, cleaning out IV lines and feed tubes, wound cleaning, renal dialysis and plasma collection. Urological and gynecological surgeries, and knee and hip replacements, may require up to 30 liters of solution for each treatment. Sodium chloride Pharma 0.9% injection bags are currently in shortage in the U.S. [1]. Most often, diarrhea kills children and elder people by dehydration. In order to replace the lost liquid, it is essential to feed extra drinks as soon as diarrhea starts. Oral rehydration therapy with oral rehydration salt (ORS) solutions is a cheap, simple and effective way to treat dehydration caused by diarrhea. It has substantially contributed to the dramatic global reduction in mortality from diarrheal disease. ORS is the name of a balanced glucose-electrolyte mixture, where each sachet with 20.5 grams contains 2.6 grams Sodium chloride Pharma, 13.5 grams anhydrous glucose, 1.5 grams potassium chloride and 2.9 grams tri Sodium chloride Pharma citrate, dihydrate [2]. Global pharmaceutical grade Sodium chloride Pharma consumption is estimated to reach 690 kt by 2019 [3]. The market is continuously growing, with North-America as the leading consumer, followed by the Asia-Pacific region and Europe. U.S., Germany and Japan are also among the world’s largest consumers. The Asia-Pacific region with China, India, Indonesia, Vietnam, etc. is the fastest growing market across the world, followed by North-America and Europe. By 2021, an annual growth rate of approximately 6% of the worldwide dialysis patients is expected. The overall pharmaceutical grade Sodium chloride Pharma market will continue to grow with a compound annual growth rate (CAGR) of more than 5% in terms of volume. It is estimated to reach 1,000 kt by 2025, making the Asia-Pacific region, Africa, South-America, Eastern Europe, and the Russian Commonwealth particularly attractive for new capacities or capacity expansion. At present, only around 30 companies out of hundreds of salt producers worldwide produce pharmaceutical grade Sodium chloride Pharma. One reason for this is that pharmaceutical grade Sodium chloride Pharma is a salt specialty with a market share of less than 1% of the total global salt demand. The major part goes to applications in the chemical industry, road de-icing, human and animal nutrition and water treatment. In addition, pharmaceutical salt is only suitable in the form of vacuum salt, and specific measures in production, quality monitoring and documentation are necessary. Extra certifications and qualifications are also required. Pharmaceutical grade Sodium chloride Pharma is required in injections; hemodialysis, peritoneal dialysis, & hemofiltration solutions, oral rehydration salts (ORS), channeling agents/ osmotic agent, mechanical cleansing solutions, and others (dietary formulations and infant formulations). The report covers qualitative aspect and detailed volume (kilotons) and value ($Million) forecasts along with its applications and region. This study aims at estimating the global market for 2013 and to project the expected demand of the same by 2019. This market research study provides a detailed qualitative and quantitative analysis of the global pharmaceutical grade Sodium chloride Pharma market. It provides a comprehensive review of key market drivers, restraints, opportunities, winning imperatives, challenges, and key issues in the market. The market is segmented and projected for important regions, such as Asia-Pacific, Europe, North America and Rest of the World, which are further segmented for key countries in each region. This research report categorizes the global pharmaceutical grade Sodium chloride Pharma market on the basis of applications and region along with forecasting volume, value, and trends in each of the markets. On the basis of application: Pharmaceutical grade Sodium chloride Pharma is characterized on the basis of applications that include injections, hemodialysis, peritoneal dialysis, & hemofiltration solutions, oral rehydration salts (ORS), channeling agents/ osmotic agent, mechanical cleansing solutions, and others (dietary formulations and infant formulations). These applications are described in detail in this report. On the basis of region: Regional level segmentation is done for Pharmaceutical grade Sodium chloride Pharma that includes North America, Asia-Pacific, Europe and Rest of the World and further for key countries in each region that include U.S., China, Japan, India, Germany, France, and Belgium. South America, Africa and Middle East are collectively considered in Rest of the World. The pharmaceutical grade Sodium chloride Pharma market is estimated to witness a CAGR of 6.9% between 2014 and 2019 in terms of volume, and the consumption is anticipated to reach 690 KT by 2019. The report on ‘Pharmaceutical grade Sodium chloride Pharma market’ considers study by its applications. Pharmaceutical grade Sodium chloride Pharma finds its application in injections, dialysis, oral rehydration salts (ORS), pharmaceutical formulations, mechanical cleansing solutions, and others (dietary formulations and infant formulations). The market is estimated to increase significantly in Asia-Pacific due to the increasing awareness and increased spending of the region in the healthcare sector. The growing dialysis and IV solutions applications are projected to register descent CAGRs in terms of volume, during the forecast period (2014- Growing awareness, increased spending in the healthcare sector and excessive availability and accessibility makes Asia-Pacific an attractive market for capacity expansion. Asia-Pacific is the fastest growing market across the world, followed by North America and Europe. With the aforementioned opportunities, the overall pharmaceutical grade Sodium chloride Pharma market remains attractive for coming years. The key participants in this market are AkzoNobel [Sanal Pharma] (The Netherlands), K+S AG (Germany), Dominion Salt (New Zealand), Salinen Austria AG (Austria), Cargill Incorporated (U.S.), Sudsalz (Germany), Cheetham Salt (Australia) and Hub Salt (Pakistan). This report follows both top-down and bottom-up approaches to estimate and forecast the global market size. Sodium chloride Pharma, ACS, USP-EP-JP Hawkins carries high purity, pharmaceutical grade Sodium chloride Pharma. We also carry pharmaceutical grade Sodium chloride Pharma in bulk and in multiple packaging options. Appearance: White Crystals Molecular Weight: 58.44 Chemical Formula: NaCl CAS #: 7647-14-5 Solubility: 36g/100ml water at 20°C Storage Conditions: Store in tight containers at 15-30ºC Sodium chloride Pharma, ACS supplied by Hawkins, Inc. Pharmaceutical Group meets the standards of the American Chemical Society (ACS). Sodium chloride Pharma, USP-EP-JP: Sodium chloride Pharma, USP/EP/JP supplied by Hawkins, Inc. Pharmaceutical Group meets the standards of United States Pharmacopeia (USP), European Pharmacopeia (EP), and Japanese Pharmacopeia (JP) monograph standards below. Product Description Sodium chloride Pharma (Pharma Grade) is a white crystalline solid commonly known as common salt, table salt or halite, is an ionic compound with the chemical formula NaCl, representing a 1:1 ratio of Sodium chloride Pharma and chloride ions. It is one of the most abundant minerals on Earth and an essential nutrient for many animals and plants. Pharmaceutical grade Sodium chloride Pharma or pharmaceutical salt is manufactured under appropriate GMP controls norm for pharmaceutical production it is a screened, granular, white crystalline Sodium chloride Pharma manufactured under stringent process control procedures. WE GUARANTEE CONTINOUS HIGH QUALITY Sodium chloride Pharma Pharmaceutical Quality are committed to purity our customers can rely on. Salt in its purest form and without additives plays an essential role in the pharmaceutical industry, in the manufacture medical and pharmaceutical products. Active Pharmaceutical Ingredients - API Comply with the monographs of all international pharmacopoeia Registered licenses for all main markets, including US DMF P Sodium chloride Pharma Pharmaceutical Quality - API quality P+ Sodium chloride Pharma Pharmaceutical Quality - API quality Dedicated manufacturing line and finishing area - FDA accepted Manufacturing based on GMP-ICH Q7 guidelines for API What is Sodium chloride Pharma? Sodium chloride Pharma (NaCl), also known as salt, is an essential compound our body uses to: absorb and transport nutrients maintain blood pressure maintain the right balance of fluid transmit nerve signals contract and relax muscles Salt is an inorganic compound, meaning it doesn’t come from living matter. It’s made when Na (Sodium chloride Pharma) and Cl (chloride) come together to form white, crystalline cubes. Your body needs salt to function, but too little or too much salt can be harmful to your health. While salt is frequently used for cooking, it can also be found as an ingredient in foods or cleansing solutions. In medical cases, your doctor or nurse will typically introduce Sodium chloride Pharma as an injection. Read on to see why and how salt plays an important role in your body. What’s the difference between salt and Sodium chloride Pharma? Despite the fact that many people use the words Sodium chloride Pharma and salt interchangeably, they are different. Sodium chloride Pharma is a mineral and a nutrient that’s naturally occurring. Unprocessed foods like fresh vegetables, legumes, and fruit can naturally have Sodium chloride Pharma. Baking soda has Sodium chloride Pharma too. But about 75 to 90 percent of the Sodium chloride Pharma we get comes from salt already added to our foods. The weight of salt is usually a combination of 40 percent Sodium chloride Pharma and 60 percent chloride. How can you use Sodium chloride Pharma? How is Sodium chloride Pharma used medically? When your doctor prescribes a treatment with salt, they’ll use the term Sodium chloride Pharma. Sodium chloride Pharma mixed with water creates a saline solution, which has a number of different medical purposes. Medical uses for a saline solution include: Name Use IV drips to treat dehydration and electrolyte imbalances; can be mixed with sugar Saline flush injections to flush a catheter or IV after medication is administered Nasal irrigation or nasal drops to clear congestion and reduce post nasal drip and keep the nasal cavity moist Cleaning wounds to wash and rinse the area for a clean environment Eye drops to treat eye redness, tearing, and dryness Sodium chloride Pharma inhalation to help create mucus so you can cough it out It’s important to consult a doctor and only use medical saline products (excluding over-the-counter products like contact solution) as prescribed. Different types of saline solutions will contain different ratios of Sodium chloride Pharma to water. Saline that’s used for different purposes may also have additional chemicals or compounds added in. How much salt should you eat? Although salt and Sodium chloride Pharma are different, salt is 40 percent Sodium chloride Pharma and we get most of our Sodium chloride Pharma intake from salt. Many companies and restaurants use salt to preserve, season, and flavor their food. Since one teaspoon of salt has about 2,300 milligrams (mg) of Sodium chloride Pharma, it’s easy to go over the daily value. According to the CDCTrusted Source, the average American eats over 3,400 mg each day. You can limit your Sodium chloride Pharma intake by eating unprocessed foods. You may also find it easier to manage your Sodium chloride Pharma intake by making more meals at home. The American Dietary Guidelines recommendTrusted Source that Americans consume less than 2,300 mg of Sodium chloride Pharma per day. Low- Sodium chloride Pharma diet Your doctor may suggest sticking to a low- Sodium chloride Pharma diet if you’re at risk for high blood pressure or heart disease. If you have heart disease, you should try to consume less than 2,000 mg of Sodium chloride Pharma per day, although the American Heart Association (AHA) recommends keeping it under 1,500 mg. Eliminating processed foods like sausages and ready-made meals may make maintaining this number easier. Top ten low- Sodium chloride Pharma frozen meals » What does your body use Sodium chloride Pharma for? Nutrient absorption and transportation Sodium chloride Pharma and chloride play an important role in your small intestine. Sodium chloride Pharma helps your body absorb: Maintaining resting energy Sodium chloride Pharma and potassium are electrolytes in the fluid outside and inside your cells. The balance between these particles contributes to how your cells maintain your body’s energy. It’s also how nerves send signals to the brain, your muscles contract, and your heart functions. Maintaining blood pressure and hydration Your kidneys, brain, and adrenal glands work together to regulate the amount of Sodium chloride Pharma in your body. Chemical signals stimulate the kidney to either hold on to water so it can be reabsorbed into the bloodstream or get rid of excess water through the urine. When there’s too much Sodium chloride Pharma in your bloodstream, your brain signals your kidneys to release more water into your blood circulation. This leads to an increase in blood volume and blood pressure. Decreasing your Sodium chloride Pharma intake can lead to less water being absorbed into the bloodstream. The result is a lower blood pressure. Side effects For the most part, Sodium chloride Pharma isn’t a health hazard, but in excessive amounts it can irritate your: Excess salt While Sodium chloride Pharma is essential, it’s also in large amounts of almost everything we eat. Eating too much salt is linked to: Too little Sodium chloride Pharma Sodium chloride Pharma deficiency is usually a sign of an underlying disorder. The name for this condition is hyponatremia. It can be due to: About 75 to 90 percent of our Sodium chloride Pharma intake comes from salt, or Sodium chloride Pharma. Salt provides an essential mineral (Sodium chloride Pharma) that our bodies use for functions such as maintaining blood pressure and absorbing nutrients. You can also use salt for seasoning foods, cleaning your household items, and addressing certain medical issues. The American Dietary Guidelines suggest you eat less than 2,300 mg of Sodium chloride Pharma per day. You can do this by eating less processed foods, like cold cuts and prepackaged foods, and cooking meals at home. What foods have the least amount of Sodium chloride Pharma? » Too much salt can lead to bigger health concerns like high blood pressure, heart disease, and kidney disease. Lowering your salt intake while increasing how much potassium you get can help lower your risk for those conditions. You should consult your doctor before adding more Sodium chloride Pharma to your diet. Most people exceed the recommended amount, but people who drink excessive amounts of water, have persistent diarrhea, or participate in long endurance events may have Sodium chloride Pharma deficiency. In these cases, good oral hydration may help. In more severe cases, a healthcare professional may need to provide intravenous (IV) saline solution to restore hydration and electrolytes. Sodium chloride Pharma Sodium chloride Pharma (NaCl), commonly known as salt, is one of the most abundant minerals on Earth and an essential nutrient for many animals and plants. It is naturally found in seawater and in underground rock formations. What is Sodium chloride Pharma? Sodium chloride Pharma is the chemical name for salt. Sodium chloride Pharma is an electrolyte that regulates the amount of water in your body. Sodium chloride Pharma also plays a part in nerve impulses and muscle contractions. Sodium chloride Pharma is used to treat or prevent Sodium chloride Pharma loss caused by dehydration, excessive sweating, or other causes. Sodium chloride Pharma may also be used for purposes not listed in this medication guide. Important Information You should not take Sodium chloride Pharma if you have ever had an allergic reaction to it, or if you have high Sodium chloride Pharma levels in your blood. Before you take Sodium chloride Pharma, tell your doctor if you have high blood pressure, kidney or liver disease, fluid retention (especially around your legs or your lungs), congestive heart failure, preeclampsia of pregnancy if you are on a low-salt diet, or if you are allergic to any foods or drugs. Tell your doctor if you are pregnant or breast-feeding. Stop using Sodium chloride Pharma and call your doctor at once if you have stomach pain, nausea and vomiting, or swelling in your hands or feet. Call your doctor if your symptoms do not improve, or if they get worse while using Sodium chloride Pharma. Before taking this medicine You should not take Sodium chloride Pharma if you have ever had an allergic reaction to it, or if you have high Sodium chloride Pharma levels in your blood. To make sure you can safely take Sodium chloride Pharma, tell your doctor if you have any of these other conditions: FDA pregnancy category C. It is not known whether Sodium chloride Pharma will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. It is not known whether Sodium chloride Pharma passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. How should I take Sodium chloride Pharma? Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label. Take Sodium chloride Pharma with a full glass (8 ounces) of water. Sodium chloride Pharma may be taken with or without food. To be sure this medication is helping your condition, your blood may need to be tested often. Visit your doctor regularly. Do not share this medication with another person, even if they have the same symptoms you have. Call your doctor if your symptoms do not improve, or if they get worse while using Sodium chloride Pharma. What should I avoid while taking Sodium chloride Pharma? Avoid becoming overheated or dehydrated during exercise and in hot weather. Follow your doctor's instructions about the type and amount of liquids you should drink. In some cases, drinking too much liquid can be as unsafe as not drinking enough. Sodium chloride Pharma side effects Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat. Stop using Sodium chloride Pharma and call your doctor at once if you have a serious side effect such as: This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. See also: Sodium chloride Pharma side effects (in more detail) What other drugs will affect Sodium chloride Pharma? There may be other drugs that can interact with Sodium chloride Pharma. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor. See also: Sodium chloride Pharma drug interactions (in more detail) Further information Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances. Sodium chloride Pharma (NaCl) What is Sodium chloride Pharma? Sodium chloride Pharma is an ionic compound in which the Sodium chloride Pharma and chloride ions are in the ratio of 1:1. It is commonly called table salt, common salt or halite (the mineral form of common salt). It is the salt which is mainly responsible for the salinity of seawater and for the extracellular fluid which is present in many multi-cellular organisms. It finds its application from household to industrial processes. Seawater is a major source of this salt. The chemical formula of Sodium chloride Pharma is NaCl. The Occurrence of Sodium chloride Pharma Mostly all the chemical compounds which consist of chlorine or Sodium chloride Pharma is usually derived from salts. It is distributed abundantly in nature. Salt is a major ingredient of the dissolved materials in seawater. Pure salt can be obtained from mineral halite. Sodium chloride Pharma is obtained by mining the deposits and brine solution is obtained by passing water into the deposits. Hence the salts get dissolved then the solution is pumped out. Evaporation of the sea water is one of the major processes used to obtain salt and is most widely followed in countries like India. The crystals obtained usually consists of impurities such as calcium sulfate, Sodium chloride Pharma sulfate etc. Pure crystals are obtained by dissolving the salts with little water and filtering the solution. Preparation of Sodium chloride Pharma However, Sodium chloride Pharma and chlorine respond together to generate a substance that is familiar to nearly everybody in the globe that is Sodium chloride Pharma, or table salt, or common salt. 2Na(s) + Cl2(g) → 2NaCl(s) Properties of Sodium chloride Pharma It is easily soluble in water and partially soluble or insoluble in other liquids. They are white crystals which do not have an odour but possess a taste. In its aqueous state NaCl acts as a good conductor of electricity due to the free movement of the ions. It has a melting point of 801°C and a boiling point of 1,413°C. Sodium chloride Pharma Crystal Structure Sodium chloride Pharma Crystal Structure Uses of Sodium chloride Pharma It is widely used in food industries as a food preservative and as a flavour enhancer. It is a major raw material in the industrial manufacturing of various chemicals such as Sodium chloride Pharma carbonate, Sodium chloride Pharma hydrogen carbonate etc. This salt is used in glass production. In cold countries, it is used to prevent the build-up of ice on roads, bridges etc which is important for safe driving conditions. Frequently Asked Questions – FAQs What is Sodium chloride Pharma used for? The basic compound used by our body to digest and transport nutrients is Sodium chloride Pharma ( NaCl), also known as salt. Preservation of blood pressure. Keeping the correct fluid balance. Why the formula of Sodium chloride Pharma is NaCl? If Sodium chloride Pharma atoms interact with chlorine atoms, Sodium chloride Pharma is formed. Sodium chloride Pharma will donate an electron (which is a negative-charged particle) to chlorine as this happens. The chemical formula for Sodium chloride Pharma is NaCl, indicating that there is precisely one chloride atom for every Sodium chloride Pharma atom present. Does Sodium chloride Pharma kill bacteria? Sodium chloride Pharma is not only used for a number of different things, but is a good antibacterial agent as well. An antibacterial agent is one that prevents bacteria from developing and multiplying. What is the primary composition of NaCl? Formula and structure: NaCl is the molecular formula of Sodium chloride Pharma and 58.44 g / mol is its molar mass. It is an ionic compound which consists of a chloride anion (Cl-) and a Sodium chloride Pharma cation (Na+).
SODIUM CHLORITE
SODIUM CHLORITE Sodium chlorite Jump to navigationJump to search Sodium chlorite Na+.svg Chlorition.png The sodium cation Space-filling model of the chlorite anion Sodium chlorite 450g.jpg Names IUPAC name Sodium chlorite Other names Chlorous acid, sodium salt Textone Identifiers CAS Number 7758-19-2 check 49658-21-1 (trihydrate) ☒ 3D model (JSmol) Interactive image ChEBI CHEBI:78667 ☒ ChemSpider 22860 check ECHA InfoCard 100.028.942 Edit this at Wikidata EC Number 231-836-6 KEGG C19523 ☒ PubChem CID 23668197 RTECS number VZ4800000 UNII G538EBV4VF check UN number 1496 CompTox Dashboard (EPA) DTXSID8021272 Edit this at Wikidata InChI[show] SMILES[show] Properties Chemical formula NaClO2 Molar mass 90.442 g/mol (anhydrous) 144.487 g/mol (trihydrate) Appearance white solid Odor odorless Density 2.468 g/cm3, solid Melting point anhydrous decomposes at 180–200 °C trihydrate decomposes at 38 °C Solubility in water 75.8 g/100 mL (25 °C) 122 g/100 mL (60 °C) Solubility slightly soluble in methanol, ethanol Acidity (pKa) 10-11 Structure Crystal structure monoclinic Thermochemistry Std enthalpy of formation (ΔfH⦵298) -307.0 kJ/mol Pharmacology ATC code D03AX11 (WHO) Hazards Safety data sheet SDS GHS pictograms GHS03: OxidizingGHS05: CorrosiveGHS06: ToxicGHS09: Environmental hazard GHS Signal word Danger GHS hazard statements H272, H301, H310, H330, H314, H318, H400 GHS precautionary statements P210, P220, P221, P260, P262, P264, P270, P271, P273, P280, P284, P301+330+331, P303+361+353, P305+351+338, P310, P361, P363, P370+378, P391, P403+233, P405, P501 Ingestion hazard Category 3 Inhalation hazard Category 2 Eye hazard Category 1 Skin hazard Category 1B NFPA 704 (fire diamond) NFPA 704 four-colored diamond 021OX Flash point Non-flammable Lethal dose or concentration (LD, LC): LD50 (median dose) 350 mg/kg (rat, oral) Related compounds Other anions Sodium chloride Sodium hypochlorite Sodium chlorate Sodium perchlorate Other cations Potassium chlorite Barium chlorite Related compounds Chlorine dioxide Chlorous acid Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ☒ verify (what is check☒ ?) Infobox references Sodium chlorite (NaClO2) is a chemical compound used in the manufacturing of paper and as a disinfectant. Contents 1 Use 1.1 Chemical reagent 1.2 Acidified sodium chlorite 1.3 Use in public crises 2 Safety 3 Toxicity 4 Manufacture 5 General references 6 References 7 External links Use The main application of sodium chlorite is the generation of chlorine dioxide for bleaching and stripping of textiles, pulp, and paper. It is also used for disinfection of municipal water treatment plants after conversion to chlorine dioxide.[1]:2 An advantage in this application, as compared to the more commonly used chlorine, is that trihalomethanes (such as chloroform) are not produced from organic contaminants.[1]:25,33 Chlorine dioxide generated from sodium chlorite is approved by FDA under some conditions for disinfecting water used to wash fruits, vegetables, and poultry.[2][full citation needed] Sodium chlorite, NaClO2, sometimes in combination with zinc chloride, also finds application as a component in therapeutic rinses, mouthwashes,[3][4] toothpastes and gels, mouth sprays, as preservative in eye drops,[5] and in contact lens cleaning solution under the trade name Purite. It is also used for sanitizing air ducts and HVAC/R systems and animal containment areas (walls, floors, and other surfaces). Chemical reagent In organic synthesis, sodium chlorite is frequently used as a reagent in the Pinnick oxidation for the oxidation of aldehydes to carboxylic acids. The reaction is usually performed in monosodium phosphate buffered solution in the presence of a chlorine scavenger (usually 2-methyl-2-butene).[6] In 2005, sodium chlorite was used as an oxidizing agent to convert alkyl furans to the corresponding 4-oxo-2-alkenoic acids in a simple one pot synthesis.[7] Acidified sodium chlorite Mixing sodium chlorite solution with a weak food-grade acid solution (commonly citric acid), both stable, produces short-lived acidified sodium chlorite (ASC) which has potent decontaminating properties. Upon mixing the main active ingredient, chlorous acid is produced in equilibrium with chlorite anion. The proportion varies with pH, temperature, and other factors, ranging from approximately 5–35% chlorous acid with 65–95% chlorite; more acidic solutions result in a higher proportion of chlorous acid. Chlorous acid breaks down to chlorine dioxide which in turn breaks down to chlorite anion and ultimately chloride anion. ASC is used for sanitation of the hard surfaces which come in contact with food and as a wash or rinse for a variety of foods including red meat, poultry, seafood, fruits and vegetables. Because the oxo-chlorine compounds are unstable when properly prepared, there should be no measurable residue on food if treated appropriately.[8][9] ASC also is used as a teat dip for control of mastitis in dairy cattle.[10] Use in public crises The U.S. Army Natick Soldier Research, Development, and Engineering Center produced a portable "no power required" method of generating chlorine dioxide, known as ClO2, gas, described as one of the best biocides available for combating contaminants, which range from benign microbes and food pathogens to Category A Bioterror agents. In the weeks after the 9/11 attacks when anthrax was sent in letters to public officials, hazardous materials teams used ClO2 to decontaminate the Hart Senate Office Building, and the Brentwood Postal Facility.[11] In addressing the COVID-19 pandemic, the U.S. Environmental Protection Agency has posted a list of many disinfectants that meet its criteria for use in environmental measures against the causative coronavirus.[12][13] Some are based on sodium chlorite that is activated into chlorine dioxide, though differing formulations are used in each product. Many other products on the EPA list contain sodium hypochlorite, which is similar in name but should not be confused with sodium chlorite because they have very different modes of chemical action. Safety Sodium chlorite, like many oxidizing agents, should be protected from inadvertent contamination by organic materials to avoid the formation of an explosive mixture. The chemical is stable in pure form and does not explode on percussive impact, unless organic contaminants are present, such as on a greasy hammer striking the chemical on an anvil.[14] It also easily ignites by friction if combined with a reducing agent like powdered sugar, sulfur or red phosphorus. Toxicity Sodium chlorite is a strong oxidant and can therefore be expected to cause clinical symptoms similar to the well known sodium chlorate: methemoglobinemia, hemolysis, kidney failure.[15] A dose of 10-15 grams of sodium chlorate can be lethal.[16] Methemoglobemia had been demonstrated in rats and cats,[17] and recent studies by the EMEA have confirmed that the clinical symptomatology is very similar to the one caused by sodium chlorate in rats, mice, rabbits, and green monkeys.[18] There is only one human case in the medical literature of chlorite poisoning.[19] It seems to confirm that the toxicity is equal to sodium chlorate. From the analogy with sodium chlorate, even small amounts of about 1 gram can be expected to cause nausea, vomiting and even life-threatening hemolysis in glucose-6-phosphate dehydrogenase deficient persons. The EPA has set a maximum contaminant level of 1 milligram of chlorite per liter (1 mg/L) in drinking water.[20] Sellers of “Miracle Mineral Solution”, a mixture of sodium chlorite and citric acid also known as "MMS" that is promoted as a cure-all have been convicted, fined, or otherwise disciplined in multiple jurisdictions around the world. MMS products were variously referred to as snake oil and complete quackery. The U.S. Food and Drug Administration has issued multiple warnings against consuming MMS.[21] [22] [23][24] [25][26] [27][28][29] Manufacture The free acid, chlorous acid, HClO2, is only stable at low concentrations. Since it cannot be concentrated, it is not a commercial product. However, the corresponding sodium salt, sodium chlorite, NaClO2 is stable and inexpensive enough to be commercially available. The corresponding salts of heavy metals (Ag+, Hg+, Tl+, Pb2+, and also Cu2+ and NH4+) decompose explosively with heat or shock. Sodium chlorite is derived indirectly from sodium chlorate, NaClO3. First, sodium chlorate is reduced to chlorine dioxide, typically in a strong acid solution using reducing agents such as sodium sulfite, sulfur dioxide, or hydrochloric acid. This intermediate is then absorbed into a solution of aqueous sodium hydroxide where another reducing agent converts it to sodium chlorite. Even hydrogen peroxide can be used as the reducing agent, giving oxygen gas as its byproduct rather than other inorganic salts or materials that could contaminate the desired product.[30] Sodium Chlorite: Can It Be Used as Medicine? Chlorite vs. chloride Typical uses Health claims Alleged medical uses Safety and side effects Takeaway What’s sodium chlorite? Sodium chlorite — also referred to as chlorous acid, sodium salt textone, and Miracle Mineral Solution — is composed of sodium (Na), chlorine (Cl), and oxygen (O2). Many claims have been made for its use as a health supplement. However, the U.S. Food and Drug Administration (FDA)Trusted Source warns that it’s a dangerous, potentially life threatening chemical that should never be swallowed. It isn’t the same as sodium chloride Don’t confuse sodium chlorite with sodium chloride. Sodium chloride (NaCl) is also called table salt. Sodium chloride is used for many things, but it’s typically thought of as a seasoning and food preservative. Sodium chlorite (NaClO2) is typically found in an industrial setting as a bleach and a disinfectant. How’s sodium chlorite used? Sodium chlorite is marketed to both consumers and industries for various uses. Some consumer uses of sodium chlorite include: water treatment and purification surface cleaner for areas of food preparation antimicrobial treatment for food, especially seafood Larger concentrations of sodium chlorite are commonly used for industrial purposes, such as: bleaching and stripping of textiles, pulp, and paper sterilizing agent used in water treatment plants Are there any health benefits to sodium chlorite? Sodium chlorite has been promoted as a health supplement and a treatment for various illnesses, such as: common cold arthritis HIV malaria cancer hepatitis amyotrophic lateral sclerosis (ALS) While there are anecdotal reports from people who claim to have experienced medical relief by ingesting sodium chlorite solutions, there’s no reliable scientific evidence showing a benefit. The FDA issued a warning in 2019 to not drink sodium chlorite products, stating they are dangerous.Trusted Source Promoted health benefits Despite the lack of evidence supporting the use of sodium chlorite as a medication, some continue to support this chemical as a form of alternative medicine. Of these supporters, people with ALS — also known as Lou Gehrig’s disease — report the most positive benefits from sodium chlorite. ALS is a rare neurological disease that progressively leads to: muscle weakness impaired motor function muscle cramps slurred speech Eventually this condition can shut down vital parts of the body. Only about 10 percent of people with this condition live for longer than 10 years following diagnosis. People with ALS who use sodium chlorite report positive benefits, including: increased muscle activity clearer speech slowed rate of ALS progression improved flexibility improved motor functions, balance, and speed of movement Sodium chlorite received approval in the European Union as an “orphan drug” in the treatment of ALS. These drugs are usually used for rare conditions and don’t always require proven safety and effectiveness. A small number of studies have evaluated sodium chlorite in people with ALS, but the results are too preliminary to know if it’s beneficial. Is it safe to ingest sodium chlorite? Ingesting sodium chlorite as a form of alternative medicine for extended periods of time or in larger dosages is unsafe and can cause a variety of symptoms, including: fatigue diarrhea headache nausea excess saliva insomnia dehydration lowered blood pressure In addition to these symptoms, there are more serious health problems that healthcare providers warn may result from use of this chemical, such as: worsening of ALS skin burns nosebleeds hoarse throat coughing bronchitis shortness of breath In high concentrations, sodium chlorite is typically used as a bleach and a disinfectant. Sodium chlorite can be supplied either as a solid or a solution. Both forms are potentially dangerous and require a high degree of safety and skill during storage and handling. Sodium chlorite is a white flaky salt prepared at a concentration of 80%. It is extremely reactive and will explode in a violent reaction on contact with organic substances including basic items such as gloves and clothing, spillage control materials such as sawdust and cotton waste, or even oil and grease. Heat, friction or just impact can lead to an explosion, so the solid should be dissolved in water to form a solution as quickly as possible. In practice the dry form is simply too dangerous to transport, store and handle for normal WTP use, so liquid sodium chlorite is normally employed. Sodium chlorite is a highly corrosive liquid that requires careful handling to avoid damage to pipe work and equipment. Spillages of sodium chlorite must be washed away before they evaporate to leave the flammable dry residue. It has to be stored under temperature controlled conditions and is supplied at a concentration of 25–26% w/w, which gives the sodium chlorite optimum storage characteristics. At this concentration it still freezes at −15°C and is also explosive at relatively low temperatures and so should be maintained at below 40°C (Cowley, 1993). The solution is stable under neutral to slightly acidic conditions but will decay under more acidic conditions which can be prevented by adding a small amount of alkalinity (<10 mg CaCO3 L−1). However, it will also decay if the alkalinity buffers the solution above pH 8.0 (Eq. 32.6), so pH control during storage is an important consideration. Chlorate is present as an impurity in most sodium chlorite products with contamination levels usually 2–3% by weight of chlorite. [32.6] Chlorine dioxide has a relatively short half life and so is made up as required at a concentration of 1g L−1 if used in open systems or 10 g L−1 if used in enclosed pressurized systems. It is produced by reacting chlorine gas or a solution of chlorine with sodium chlorite in a glass mixing chamber which is filled with porcelain Raschig rings or Teflon® chips (Eq. 32.5). Stoichiometrically 0.5 kg of Cl2 and 1.34 kg NaClO2 are required to produce 1 kg of ClO2 (Fig. 32.1; Black and Veatch Corporation, 2010). Once prepared, ClO2 can be photo-chemically degraded in sunlight to form chlorate, chlorite, hydrogen peroxide, oxygen and chlorine, and so it must be stored and used in the dark. Similarly it is destroyed by UV light. Sign in to download full-size image Figure 32.1. Schematic diagram of the generation and use of chlorine dioxide using chlorine gas. Alternatively chlorine dioxide can be produced by reacting the sodium chlorite with hydrochloric acid. However, this process uses 1.25 times more NaClO2 than the chlorine reaction to produce the same weight of ClO2 (Eq. 32.7). Stoichiometrically 0.54 kg of HCl and 1.67 kg NaClO2 are required to produce 1 kg of ClO2, although in practice 50% more NaClO2 is required and possibly up to three times the amount of HCl may be needed to lower the pH sufficiently for the reaction to occur at pH ≤0.5 (Twort et al., 2000). [32.7] Generators are normally rented so when this is added to the cost of sodium chlorite, then chlorine dioxide disinfection is expensive, even taking into consideration that smaller doses are required compared to either chlorine or chloramines. Contact tank designs and the use of either injectors or diffusers are very similar to those used for chlorination (see Ch. 31, p. 580). However, care must be taken not to allow chlorine dioxide to escape to the atmosphere, so open pipes or channels should not be used at high ClO2 concentrations. Further details on the generation and use of chlorine dioxide are given in Gates (1998). General description The acidified solution of sodium chlorite has been tested for the antimicrobial action on the broiler carcasses. It was found to be effective in the reduction of natural bioburden in a prechill procedure..[3] Application Sodium chlorite may be used in the synthesis of chlorine dioxide[1] and as a hydroxylating agent for the hydroxylation of androstenedione (steroid).[2] Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ☒ verify (what is check☒ ?) Infobox references Sodium chlorite (NaClO2) is a chemical compound used in the manufacturing of paper and as a disinfectant. Contents 1 Use 1.1 Chemical reagent 1.2 Acidified sodium chlorite 1.3 Use in public crises 2 Safety 3 Toxicity 4 Manufacture 5 General references 6 References 7 External links Use The main application of sodium chlorite is the generation of chlorine dioxide for bleaching and stripping of textiles, pulp, and paper. It is also used for disinfection of municipal water treatment plants after conversion to chlorine dioxide.[1]:2 An advantage in this application, as compared to the more commonly used chlorine, is that trihalomethanes (such as chloroform) are not produced from organic contaminants.[1]:25,33 Chlorine dioxide generated from sodium chlorite is approved by FDA under some conditions for disinfecting water used to wash fruits, vegetables, and poultry.[2][full citation needed] Sodium chlorite, NaClO2, sometimes in combination with zinc chloride, also finds application as a component in therapeutic rinses, mouthwashes,[3][4] toothpastes and gels, mouth sprays, as preservative in eye drops,[5] and in contact lens cleaning solution under the trade name Purite. It is also used for sanitizing air ducts and HVAC/R systems and animal containment areas (walls, floors, and other surfaces). Chemical reagent In organic synthesis, sodium chlorite is frequently used as a reagent in the Pinnick oxidation for the oxidation of aldehydes to carboxylic acids. The reaction is usually performed in monosodium phosphate buffered solution in the presence of a chlorine scavenger (usually 2-methyl-2-butene).[6] In 2005, sodium chlorite was used as an oxidizing agent to convert alkyl furans to the corresponding 4-oxo-2-alkenoic acids in a simple one pot synthesis.[7] Acidified sodium chlorite Mixing sodium chlorite solution with a weak food-grade acid solution (commonly citric acid), both stable, produces short-lived acidified sodium chlorite (ASC) which has potent decontaminating properties. Upon mixing the main active ingredient, chlorous acid is produced in equilibrium with chlorite anion. The proportion varies with pH, temperature, and other factors, ranging from approximately 5–35% chlorous acid with 65–95% chlorite; more acidic solutions result in a higher proportion of chlorous acid. Chlorous acid breaks down to chlorine dioxide which in turn breaks down to chlorite anion and ultimately chloride anion. ASC is used for sanitation of the hard surfaces which come in contact with food and as a wash or rinse for a variety of foods including red meat, poultry, seafood, fruits and vegetables. Because the oxo-chlorine compounds are unstable when properly prepared, there should be no measurable residue on food if treated appropriately.[8][9] ASC also is used as a teat dip for control of mastitis in dairy cattle.[10] Use in public crises The U.S. Army Natick Soldier Research, Development, and Engineering Center produced a portable "no power required" method of generating chlorine dioxide, known as ClO2, gas, described as one of the best biocides available for combating contaminants, which range from benign microbes and food pathogens to Category A Bioterror agents. In the weeks after the 9/11 attacks when anthrax was sent in letters to public officials, hazardous materials teams used ClO2 to decontaminate the Hart Senate Office Building, and the Brentwood Postal Facility.[11] In addressing the COVID-19 pandemic, the U.S. Environmental Protection Agency has posted a list of many disinfectants that meet its criteria for use in environmental measures against the causative coronavirus.[12][13] Some are based on sodium chlorite that is activated into chlorine dioxide, though differing formulations are used in each product. Many other products on the EPA list contain sodium hypochlorite, which is similar in name but should not be confused with sodium chlorite because they have very different modes of chemical action. Safety Sodium chlorite, like many oxidizing agents, should be protected from inadvertent contamination by organic materials to avoid the formation of an explosive mixture. The chemical is stable in pure form and does not explode on percussive impact, unless organic contaminants are present, such as on a greasy hammer striking the chemical on an anvil.[14] It also easily ignites by friction if combined with a reducing agent like powdered sugar, sulfur or red phosphorus. Toxicity Sodium chlorite is a strong oxidant and can therefore be expected to cause clinical symptoms similar to the well known sodium chlorate: methemoglobinemia, hemolysis, kidney failure.[15] A dose of 10-15 grams of sodium chlorate can be lethal.[16] Methemoglobemia had been demonstrated in rats and cats,[17] and recent studies by the EMEA have confirmed that the clinical symptomatology is very similar to the one caused by sodium chlorate in rats, mice, rabbits, and green monkeys.[18] There is only one human case in the medical literature of chlorite poisoning.[19] It seems to confirm that the toxicity is equal to sodium chlorate. From the analogy with sodium chlorate, even small amounts of about 1 gram can be expected to cause nausea, vomiting and even life-threatening hemolysis in glucose-6-phosphate dehydrogenase deficient persons. The EPA has set a maximum contaminant level of 1 milligram of chlorite per liter (1 mg/L) in drinking water.[20] Sellers of “Miracle Mineral Solution”, a mixture of sodium chlorite and citric acid also known as "MMS" that is promoted as a cure-all have been convicted, fined, or otherwise disciplined in multiple jurisdictions around the world. MMS products were variously referred to as snake oil and complete quackery. The U.S. Food and Drug Administration has issued multiple warnings against consuming MMS.[21] [22] [23][24] [25][26] [27][28][29] Manufacture The free acid, chlorous acid, HClO2, is only stable at low concentrations. Since it cannot be concentrated, it is not a commercial product. However, the corresponding sodium salt, sodium chlorite, NaClO2 is stable and inexpensive enough to be commercially available. The corresponding salts of heavy metals (Ag+, Hg+, Tl+, Pb2+, and also Cu2+ and NH4+) decompose explosively with heat or shock. Sodium chlorite is derived indirectly from sodium chlorate, NaClO3. First, sodium chlorate is reduced to chlorine dioxide, typically in a strong acid solution using reducing agents such as sodium sulfite, sulfur dioxide, or hydrochloric acid. This intermediate is then absorbed into a solution of aqueous sodium hydroxide where another reducing agent converts it to sodium chlorite. Even hydrogen peroxide can be used as the reducing agent, giving oxygen gas as its byproduct rather than other inorganic salts or materials that could contaminate the desired product.[30] Sodium Chlorite: Can It Be Used as Medicine? Chlorite vs. chloride Typical uses Health claims Alleged medical uses Safety and side effects Takeaway What’s sodium chlorite? Sodium chlorite — also referred to as chlorous acid, sodium salt textone, and Miracle Mineral Solution — is composed of sodium (Na), chlorine (Cl), and oxygen (O2). Many claims have been made for its use as a health supplement. However, the U.S. Food and Drug Administration (FDA)Trusted Source warns that it’s a dangerous, potentially life threatening chemical that should never be swallowed. It isn’t the same as sodium chloride Don’t confuse sodium chlorite with sodium chloride. Sodium chloride (NaCl) is also called table salt. Sodium chloride is used for many things, but it’s typically thought of as a seasoning and food preservative. Sodium chlorite (NaClO2) is typically found in an industrial setting as a bleach and a disinfectant. How’s sodium chlorite used? Sodium chlorite is marketed to both consumers and industries for various uses. Some consumer uses of sodium chlorite include: water treatment and purification surface cleaner for areas of food preparation antimicrobial treatment for food, especially seafood Larger concentrations of sodium chlorite are commonly used for industrial purposes, such as: bleaching and stripping of textiles, pulp, and paper sterilizing agent used in water treatment plants Are there any health benefits to sodium chlorite? Sodium chlorite has been promoted as a health supplement and a treatment for various illnesses, such as: common cold arthritis HIV malaria cancer hepatitis amyotrophic lateral sclerosis (ALS) While there are anecdotal reports from people who claim to have experienced medical relief by ingesting sodium chlorite solutions, there’s no reliable scientific evidence showing a benefit. The FDA issued a warning in 2019 to not drink sodium chlorite products, stating they are dangerous.Trusted Source Promoted health benefits Despite the lack of evidence supporting the use of sodium chlorite as a medication, some continue to support this chemical as a form of alternative medicine. Of these supporters, people with ALS — also known as Lou Gehrig’s disease — report the most positive benefits from sodium chlorite. ALS is a rare neurological disease that progressively leads to: muscle weakness impaired motor function muscle cramps slurred speech Eventually this condition can shut down vital parts of the body. Only about 10 percent of people with this condition live for longer than 10 years following diagnosis. People with ALS who use sodium chlorite report positive benefits, including: increased muscle activity clearer speech slowed rate of ALS progression improved flexibility improved motor functions, balance, and speed of movement Sodium chlorite received approval in the European Union as an “orphan drug” in the treatment of ALS. These drugs are usually used for rare conditions and don’t always require proven safety and effectiveness. A small number of studies have evaluated sodium chlorite in people with ALS, but the results are too preliminary to know if it’s beneficial. Is it safe to ingest sodium chlorite? Ingesting sodium chlorite as a form of alternative medicine for extended periods of time or in larger dosages is unsafe and can cause a variety of symptoms, including: fatigue diarrhea headache nausea excess saliva insomnia dehydration lowered blood pressure In addition to these symptoms, there are more serious health problems that healthcare providers warn may result from use of this chemical, such as: worsening of ALS skin burns nosebleeds hoarse throat coughing bronchitis shortness of breath In high concentrations, sodium chlorite is typically used as a bleach and a disinfectant. Sodium chlorite can be supplied either as a solid or a solution. Both forms are potentially dangerous and require a high degree of safety and skill during storage and handling. Sodium chlorite is a white flaky salt prepared at a concentration of 80%. It is extremely reactive and will explode in a violent reaction on contact with organic substances including basic items such as gloves and clothing, spillage control materials such as sawdust and cotton waste, or even oil and grease. Heat, friction or just impact can lead to an explosion, so the solid should be dissolved in water to form a solution as quickly as possible. In practice the dry form is simply too dangerous to transport, store and handle for normal WTP use, so liquid sodium chlorite is normally employed. Sodium chlorite is a highly corrosive liquid that requires careful handling to avoid damage to pipe work and equipment. Spillages of sodium chlorite must be washed away before they evaporate to leave the flammable dry residue. It has to be stored under temperature controlled conditions and is supplied at a concentration of 25–26% w/w, which gives the sodium chlorite optimum storage characteristics. At this concentration it still freezes at −15°C and is also explosive at relatively low temperatures and so should be maintained at below 40°C (Cowley, 1993). The solution is stable under neutral to slightly acidic conditions but will decay under more acidic conditions which can be prevented by adding a small amount of alkalinity (<10 mg CaCO3 L−1). However, it will also decay if the alkalinity buffers the solution above pH 8.0 (Eq. 32.6), so pH control during storage is an important consideration. Chlorate is present as an impurity in most sodium chlorite products with contamination levels usually 2–3% by weight of chlorite. [32.6] Chlorine dioxide has a relatively short half life and so is made up as required at a concentration of 1g L−1 if used in open systems or 10 g L−1 if used in enclosed pressurized systems. It is produced by reacting chlorine gas or a solution of chlorine with sodium chlorite in a glass mixing chamber which is filled with porcelain Raschig rings or Teflon® chips (Eq. 32.5). Stoichiometrically 0.5 kg of Cl2 and 1.34 kg NaClO2 are required to produce 1 kg of ClO2 (Fig. 32.1; Black and Veatch Corporation, 2010). Once prepared, ClO2 can be photo-chemically degraded in sunlight to form chlorate, chlorite, hydrogen peroxide, oxygen and chlorine, and so it must be stored and used in the dark. Similarly it is destroyed by UV light. Sign in to download full-size image Figure 32.1. Schematic diagram of the generation and use of chlorine dioxide using chlorine gas. Alternatively chlorine dioxide can be produced by reacting the sodium chlorite with hydrochloric acid. However, this process uses 1.25 times more NaClO2 than the chlorine reaction to produce the same weight of ClO2 (Eq. 32.7). Stoichiometrically 0.54 kg of HCl and 1.67 kg NaClO2 are required to produce 1 kg of ClO2, although in practice 50% more NaClO2 is required and possibly up to three times the amount of HCl may be needed to lower the pH sufficiently for the reaction to occur at pH ≤0.5 (Twort et al., 2000). [32.7] Generators are normally rented so when this is added to the cost of sodium chlorite, then chlorine dioxide disinfection is expensive, even taking into consideration that smaller doses are required compared to either chlorine or chloramines. Contact tank designs and the use of either injectors or diffusers are very similar to those used for chlorination (see Ch. 31, p. 580). However, care must be taken not to allow chlorine dioxide to escape to the atmosphere, so open pipes or channels should not be used at high ClO2 concentrations. Further details on the generation and use of chlorine dioxide are given in Gates (1998). General description The acidified solution of sodium chlorite has been tested for the antimicrobial action on the broiler carcasses. It was found to be effective in the reduction of natural bioburden in a prechill procedure..[3] Application Sodium chlorite may be used in the synthesis of chlorine dioxide[1] and as a hydroxylating agent for the hydroxylation of androstenedione (steroid).[2]
SODIUM CHLORITE 31%
SODIUM COCAMINOPROPIONATE N° CAS : 68608-68-4 / 8033-69-0 / 12676-68-4 Nom INCI : SODIUM COCAMINOPROPIONATE N° EINECS/ELINCS : 271-795-1 Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM CITRATE
SODIUM CITRATE Sodium citrate Monosodium citrate Disodium citrate Trisodium citrate The three forms of the salt are collectively known by the E number E331. Sodium citrates are used as acidity regulators in food and drinks, and also as emulsifiers for oils. They enable cheeses to melt without becoming greasy. Sodium citrate is used to prevent donated blood from clotting in storage. It is also used in a laboratory, before an operation, to determine whether a person's blood is too thick and might cause a blood clot, or if the blood is too thin to safely operate. SODIUM CITRATE Trisodium citrate dihydrate is a salt of citric acid Use a small amount to make a melty cheese sauce out of any cheese Add to spherification liquids to neutralize the pH when needed Commonly used as a sequestrant and pH buffer in food and beverages Cold/hot soluble, practically insoluble in ethanol (96%) earn and spend points. DESCRIPTION 100% Pure Food Grade Sodium Citrate Powder (e331) for use in spherification and molecular gastronomy. Sodium Citrate (E331) is the sodium salt of citric acid. Like citric acid, it has a sour taste. Like other salts, it also has a salty taste. It is commonly known as sour salt and is mainly used as a food additive, usually for flavor or as a preservative. It gives club soda both its sour and salty flavors. It reduces the acidity of foods, so it allows spherification with strongly acidic ingredients. Sodium citrate is also used as an antioxidant in food as well as a sequestrant. It dissolves easily and acts instantaneously. OTHER DETAILS Dietary Attributes: Plant-Based, Non-GMO, Gluten-Free, Kosher (OU), Keto-friendly Ingredient List: Sodium Citrate Allergen(s): None Uses This medication is used to make the urine less acidic. Urine that is less acidic helps the kidneys get rid of uric acid, helping to prevent gout and certain types of kidney stones (urate). This medication can also prevent and treat certain metabolic problems (acidosis) caused by kidney disease. Citric acid and citrate salts (which contain potassium and sodium) belong to a class of drugs known as urinary alkalinizers. Because some conditions require you to limit your intake of potassium and sodium, your doctor's choice of product may depend on how much potassium and sodium you can take. How to use Sodium CITRATE & CITRIC Acid Shake the container well before each dose. Take this medication by mouth, usually 4 times a day or as directed by your doctor. To help prevent diarrhea and stomach upset, take each dose after a meal, and mix your prescribed dose of medication in a full glass (4 to 8 ounces or 120 to 240 milliliters) of cold water or juice just before taking, or take as directed by your doctor. Drink the entire mixture slowly. Ask your doctor or pharmacist for further instructions. The liquid form of this medication must be mixed with at least 4 ounces (120 milliliters) of water or juice before taking. Refrigerating the mixture before drinking may improve the taste. Drink more water or juice after taking this medication unless otherwise directed by your doctor. Dosage is based on your medical condition and response to treatment. Take this medication as prescribed. Do not increase your dose or take this more often without your doctor's approval. Use this medication regularly to get the most benefit from it. To help you remember, take it at the same times each day. While taking this medication, you may need to test the pH (acidity) of your urine using special paper. The pH will help determine the proper dose. Consult your doctor or pharmacist for more information. What is citric acid and sodium citrate? Citric acid and sodium citrate are both alkalinizing agents that make the urine less acidic. The combination of citric acid and sodium citrate is used to prevent gout or kidney stones, or metabolic acidosis in people with kidney problems. Citric acid and sodium citrate may also be used for other purposes not listed in this medication guide. Important Information You should not use this medication if you have kidney failure, severe heart damage (such as from a prior heart attack), Addison's disease (an adrenal gland disorder), high levels of potassium in your blood (hyperkalemia), or if you are severely dehydrated or have heat cramps. Before you take citric acid and sodium citrate, tell your doctor about all your medical conditions, especially kidney disease, heart disease, high blood pressure, a history of heart attack, urinary problems, swelling (edema), or chronic diarrhea (such as ulcerative colitis, Crohn's disease). Also tell your doctor about all other medications you use, including over-the-counter medications and household remedies. Citric acid and sodium citrate should be taken after meals to help prevent stomach or intestinal side effects. The liquid medicine should be mixed with water or juice. Drink plenty of liquids while you are taking citric acid and sodium citrate. Your treatment may include a special diet. You should become very familiar with the list of foods you should eat or avoid to help control your condition. Avoid using antacids without your doctor's advice, including household baking soda (sodium bicarbonate). Antacids that contain aluminum or sodium can interact with citric acid and sodium citrate, causing a serious electrolyte imbalance or aluminum toxicity. Avoid eating foods that are high in salt, or using extra table salt on your meals. To be sure citric acid and sodium citrate is helping your condition, your blood and urine may need to be tested often. Follow your doctor's instructions carefully and do not miss any scheduled appointments. Serious side effects of citric acid and sodium citrate include muscle twitching or cramps, swelling or weight gain, weakness, mood changes, rapid and shallow breathing, fast heart rate, restless feeling, black or bloody stools, severe diarrhea, or seizure (convulsions). Before taking this medicine You should not use this medication if you are allergic to it, or if you have: kidney failure; severe heart damage (such as from a prior heart attack); Addison's disease (an adrenal gland disorder); high levels of potassium in your blood (hyperkalemia); or if you are severely dehydrated or have heat cramps. How should I take citric acid and sodium citrate? Take this medication exactly as prescribed by your doctor. Do not take it in larger amounts or for longer than recommended. Follow the directions on your prescription label. Citric acid and sodium citrate should be taken after meals to help prevent stomach or intestinal side effects. You may also need to take the medicine at bedtime. Follow your doctor's instructions. Shake the oral solution (liquid) well just before you measure a dose. To be sure you get the correct dose, measure the liquid with a marked measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one. The liquid medicine should be mixed with at lease 4 ounces of water or juice. Drink this mixture slowly and then add a little more water to the same glass, swirl gently and drink right away. You may chill the mixed medicine to make it taste better, but do not allow it to freeze. Drink plenty of liquids while you are taking citric acid and sodium citrate. Your treatment may include a special diet. It is very important to follow the diet plan created for you by your doctor or nutrition counselor. You should become very familiar with the list of foods you should eat or avoid to help control your condition. To be sure citric acid and sodium citrate is helping your condition, your blood and urine may need to be tested often. Follow your doctor's instructions carefully and do not miss any scheduled appointments. Trisodium citrate dihydrate is a tribasic salt of citric acid. Trisodium citrate dihydrate is produced by complete neutralisation of citric acid with high purity sodium hydroxide or carbonate and subsequent crystallisation. Trisodium citrate dihydrate is widely used in foods, beverages and various technical applications mainly as buffering, sequestering or emulsifying agent.Sodium citrate dihydrate is the most widely used emulsifying salt in sliced processed cheese products. It is commonly used as a buffering agent in combination with citric acid to provide precise pH control required in many food and beverage applications.Trisodium citrate is often referred to as sodium citrate, though sodium citrate can refer to any of the three sodium salts of citric acid. Sodium citrate has a saline, mildly tart flavor. It is mildly basic and can be used along with citric acid to make biologically compatible buffers. Sodium citrate is primarily used as a food additive, usually for flavor or as a preservative. In certain varieties of club soda, sodium citrate is employed as a flavoring agent. Sodium citrate is a common ingredient in Bratwurst, and is also used to contribute a tart flavor in commercial, ready-to- drink beverages and drink mixes. It is found in gelatin mix, ice-cream, jams, sweets, milk powder, processed cheeses, carbonated beverages, and wine.Sodium Citrate is also used as an emulsifier for oils in the cheesemaking process. Sodium citrate allows cheese to melt without becoming greasy. Historically, sodium phosphate was used to keep water and fat droplets mixed when cheese is melted. Soy Products: Bakery Flavors,Table Top Product Dairy Confectionery, Fruits, Vegetables Meat, Seafood , Cereals, Snacks Desserts, Ice Cream Ready Meals, Instant Food, Fruit Preparations, Sweet Spreads Baby Food, Infant Formula Sauces, Dressings, Seasoning The main functions of citric acid and the citrates in foods and beverages can be summarized as follows: as a flavor adjunct, to improve taste as a pH control agent, e.g., for gelation control, buffering and preservative enhancement as a chelating agent to improve the action of antioxidants and prevent spoilage of foods such as seafood Beverages, Alcoholic Beverages, Carbonated Soft Drinks, Instant Drinks, Syrups, Juice Drinks, Tea and Coffee, Sports and Energy Drinks, Waters Within this market, citric acid or its salts perform several functions. The dominant application is for flavor enhancement. Many of the lemon, lime or citrus soft drinks available today use citric acid as a way of enhancing the tangy, zesty flavor consumers associate with these tropical fruit flavors. Additionally, citric acid can help provide consistency in acidity and flavor of fruit juices or fruit cordials. If used together with sodium citrate, it is possible for citric acid to help maintain the flavor of other types of soft drinks without adding to the tanginess. Sodium citrate can also provide a cool saline taste. Effervescent tablets and preparations: The reaction of citric acid and bicarbonate liberates carbon dioxide, which aids the dissolution of active ingredients and improves palatability. Effervescent systems are widely used in denture-cleaning products, as well as pain relief and vitamin tablets. Pharmaceutically active substances - many are supplied as their citrate salt. pH control: Citric acid, with sodium or potassium citrate, is an efficient buffering system used in a variety of pharmaceutical and cosmetic applications for improving stability and (where appropriate) enhancing the activity of preservatives. Flavor: The sharp, acid taste of citric acid (which is often used to enhance fruit flavors) can help mask the unpleasant, medicinal taste of pharmaceuticals. Antioxidant: The citrate ion is a powerful chelating agent for trace metal ions. Blood anticoagulant: The citrate ion will chelate calcium, thereby reducing the tendency for blood to clot. Diuretic - potassium citrate has diuretic properties. Clinical Nutrition Medical Devices OTC, Food Supplements Pharmaceutical Productscolor Cosmetics Deodorants, Fragrances Hair Care, Oral Care Skin Care Soap and Bath Products, Cleaners & Detergents, The major components of cleaning products are surfactants and builders. Other ingredients are added to provide a variety of functions, e.g., increasing cleaning performance for specific soils/surfaces, ensuring product stability, and supplying a unique identity to a product. Complex phosphates and sodium citrate are common sequestering builders. Builders enhance or maintain the cleaning efficiency of the surfactant. The primary function of builders is to reduce water hardness. This is done either by sequestration or chelation (holding hardness minerals in solution); by precipitation (forming an insoluble substance); or by ion exchange (trading electrically charged particles). Builders can also supply and maintain alkalinity, which assists cleaning, especially of acid soils; help keep removed soil from redepositing during washing, and emulsify oily and greasy soils. Dish Washing Industrial Cleaners, Laundry Care Surface Care. Trisodium citrate dihydrate occurs as white, granular crystals or as white, crystalline powder with a pleasant, salty taste. It is slightly deliquescent in moist air, freely soluble in water and practically insoluble in ethanol (96 %). Product Usage: Mainly used as food additive and preservative, The anticoagulant in blood transfusions, Used to relieve discomfort in urinary tract infections, Trisodium citrate dihydrate also works as buffering agent in food and acidity regulator as antacid, As a sequestrant - to improve the quality and stability of the food p6132-04-3roducts, As a emulsifier - to stabilize processed foods like cheese. Sodium citrate material is derived from the citric acid (sodium salts). This material is available in the colorless granular form or powdery form. This is fragrance free material and generously mixed with water, but not in the alcohol. Trisodium citrate dihydrate is not contain any food allergens and it is suitable for consumption by vegans and vegetarians. Trisodium citrate dihydrate adds enjoyable flavor in food items. It is widely used as dehydrate salt, but it provides remarkable gain in dry products where long shelf life is needed to store it. Sodium Citrate Dihydrate is generally immediately available in most volumes. High purity, submicron and nanopowder forms may be considered. American Elements produces to many standard grades when applicable, including Mil Spec (military grade); ACS, Reagent and Technical Grade; Food, Agricultural and Pharmaceutical Grade; Optical Grade, USP and EP/BP (European Pharmacopoeia/British Pharmacopoeia) and follows applicable ASTM testing standards. Typical and custom packaging is available. Additional technical, research and safety (MSDS) information is available as is a Reference Calculator for converting relevant units of measurement. Sodium citrate. It is used as flavors, stabilizing agent, buffering agent, chelating agent, nutritional supplement of buttermilk, emulsifying agent and flavoring agent in food and beverage industry;it can be used as anti-blood clotting, apophlegmatisant and diuretics in phamaceutical industry;it can replace sodium tripolyphosphate as a non-toxic detergent additives in detergent industry;it can also be used in brewing, injection, photography drugs and electroplating etc. Contact us for more information. Sodium citrate is the sodium salt of citric acid. It is white, crystalline powder or white, granular crystals, slightly deliquescent in moist air, freely soluble in water, practically insoluble in alcohol. Like citric acid, it has a sour taste. From the medical point of view, it is used as alkalinizing agent. It works by neutralizing excess acid in the blood and urine. Trisodium citrate dihydrate has been indicated for the treatment of metabolic acidosis. Sodium citrate dihydrate (C6H5Na3O7•2H2O), also known as citric trisodium salt dihydrate, or trisodium citrate dehydrate is obtained from citric acid and is available in granular or powder form having a salty but pleasant taste. Sodium citrate dihydrate is odorless and freely soluble in water, marginally deliquescent in moist air, and insoluble in alcohol. Trisodium citrate dihydrate is prepared by completely neutralizing citric acid with high purity sodium hydroxide or carbonate followed by crystallization. Global Sodium Citrate Dihydrate Market: Overview: Trisodium citrate dihydrate is a non-toxic, neutral salt having low reactivity. Trisodium citrate dihydrate shows chemically stability when stored at ambient temperatures. Sodium citrate dihydrate is totally biodegradable and disposable with the regular waste or sewage. It is widely used in the food industry inpreservatives, and as a flavoring agent. According to the FDA Select Committee, sodium citrate are regarded as safe when used in normal quantities. In the pharmaceutical industry, it is used to resist changes in the pH. Sodium citrate dihydrate also finds its use as a buffering agent, alkalizing agent, emulsifying agent, or sequestering agent. Global Sodium Citrate Dihydrate Market: Segmentation: Global sodium citrate dihydrate market is segmented into types, forms, functions, applications, manufacturing methods, and region. Types of sodium citrate dehydrate can be segmented into monosodium citrate, disodium citrate, and trisodium citrate. The global sodium citrate dihydrate market can be segmented on the basis of form into granular and crystals. Functions include regulation of pH, chelating agent, buffering agent, flavor enhancer, and emulsifying agent. Application types include food and beverage industry, cleaners and detergents, industrial applications and healthcare industry. Global sodium citrate dihydrate market is also segmented on the basis of manufacturing methods. Region-wise, global sodium citrate dihydrate market is segmented into North America, Latin America, Europe, Asia-Pacific and MEA. Global Trisodium Citrate Dihydrate Market: Region-wise Outlook: The global sodium citrate dihydrate market is expected to witness a considerable growth in CAGR between 2015 and 2025. Owing to number of favorable conditions, the focus of the major chemical companies is gradually shifting towards the growing economies. China has graduated to become the largest base for producing chemicals worldwide in terms of capacity and output. Reason being the cost benefits over the western countries in terms of production of chemical products and a high demand within the country. Moreover, the licensing procedures are comparatively shorter and the construction costs being lower than in Europe. Global Trisodium Citrate Dihydrate Market: Drivers & Restraints: Seasonal factors for beverages and new detergent applications are the principal growth drivers for the global sodium citrate dihydrate market. Fluctuations in the raw materials prices hinders the steady growth of the global sodium citrate dihydrate market. Trisodium Citrate Dihydrate (TriSodium Citrate) is commonly used to improve exercise performance and as a food additive. Trisodium citrate dihydrate's naturally a strong source of antioxidants and typically used as a natural preservative. Some have also used the ingredient in beverages to increase acidity or to emulsify cheese during the aging process. This ingredient may be added to foods and beverages or smoothies and green drinks. It is a pure white powder and has no fillers or binders, additives or preservatives. Various sizes available for personal use and quantity discounts available on bulk- packed foods and food powders for commercial uses. Only the highest quality natural food and bulk ingredients are sourced through family-owned Prescribed For Life Nutrition. Thank you for shopping with us and please come again! BENEFITS: Promotes healthy circulation and blood flow, Balances the pH levels in the body, Odorless and tasteless, 100% food grade. We use only FDA GRAS rated ingredients(Generally Recognized as Safe) that are Non-GMO (Contains NO Genetically Modified Organisms). We have size options for individual use and in volume at wholesale pricing. Sodium citrate dihydrate with chemical formula C6H5Na3O7 - 2H2O is also known as citric trisodium salt dihydrate, or trisodium citrate dehydrate. Sodium citrate dihydrate is obtained from the reaction of citric acid, high purity sodium hydroxide or carbonate followed by crystallization. Sodium citrate dihydrate is characterised as odorless and freely soluble in water, marginally deliquescent in moist air, and insoluble in alcohol. Sodium citrate dihydrate is a non-toxic, neutral salt having low reactivity. Trisodium citrate dihydrate shows chemical stability when stored at ambient temperatures. Sodium citrate dihydrate is totally biodegradable and disposable with regular waste or sewage. Globally increasing demand from the end-use industries is expected to be the key growth driver for sodium citrate dehydrate during the period of study. Geographically, Asia-Pacific dominated trisodium citrate dihydrate market driven in terms of production and consumption driven by higher demand into major end-user industry in the region. Asia-Pacific was followed by North America and Europe as second and third largest market for sodium citrate dihydrate market. Asia Pacific is projected to have fastest growth, owing to increasing consumption into its increasing industrial base demanding higher sodium citrate dihydrate. Sodium citrate, (molecular formula: Na3C6H5O7 • 2H2O) has molecular weight of 294.1, is a colorless crystal or white crystalline powder product; it is odorless, salty taste, and cool.It will lose its crystal water at 150 °C and will be decomposed at even higher temperature. It also has slight deliquescence in wet air and has weathering property upon hot air. It is soluble in water and glycerol, but insoluble in alcohol and some other organic solvents. Sodium citrate has no toxic effect, and has pH adjusting capability as well as having a good stability, and therefore can be used in the food industry. Sodium citrate has the greatest demand when being used as a food additive; As food additives, it is mainly used as flavoring agents, buffers, emulsifiers, bulking agents, stabilizers and preservatives; in addition, combination between sodium citrate and citric acid can be used in a variety of jams, jelly,Sodium citrate is currently the most important citrate. Trisodium citrate dihydrate is produced by two steps: first starch food is fermented to generate citric acid; secondly, citric acid is neutralized by alkali to generate the final products. Sodium citrate has the following excellent performance: Safe and nontoxic properties; Since the basic raw material for the preparation of sodium citrate mainly comes from the food, it is absolutely safe and reliable without causing harm to human health. The United Nations Food and Agriculture and the World Health Organization has no restriction in its daily intake, which means that this product can be considered as non- toxic food. It is biodegradable. After subjecting to the dilution of a large amount of water, sodium citrate is partially converted into citrate, which coexists with sodium citrate in the same system. Citrate is easy to subject to biological degradation at water by the action of oxygen, heat, light, bacteria and microbes. Its decomposition pathways are generally going through aconitic acid, itaconic acid, citraconic acid anhydride to be further converted to carbon dioxide and water.The ability of forming complex with metal ions. Sodium citrate has a good capability of forming complex with some metal ions such as Ca2+, Mg2+; for other ions such as Fe2+, it also has a good complex-forming ability. Excellent solubility, and the solubility increases with increasing temperature of water. It has a good capability for pH adjustment and a good buffering property. Sodium citrate is a weak acid-strong alkali salt; When combined with citrate, they can form a pH buffer with strong compatibility; therefore, this is very useful for some cases in which it is not suitable to have large change of pH value. In addition, sodium citrate also has excellent retardation performance and stability. juice, drinks, cold drinks, dairy products and pastries gelling agents, flavoring agents and nutritional supplements. During the process of clinically taking fresh blood, adding some amount of sterile sodium citrate can play a role in prevent blood clotting; this is exactly taking advantage of the features that calcium citrate can form soluble complexes with calcium ion; In the field of medicine, it is used for the in vitro anti-clotting drugs and anticoagulants drugs, phlegm drugs, and diuretics drugs during blood transfusions; Trisodium citrate dihydrate can also used for cyanide-free electroplating industry; also used as developer for photographic industry. It can be used as flavoring agents, buffering materials, emulsifiers, and stabilizer in the food industry. Moreover, it is also widely used in chemical, metallurgical industry, the absorption of sulfur dioxide exhaust with the absorption rate of 99% and regenerate liquid sulfur dioxide citrate for recycle application. Sodium citrate has a good water solubility and a excellent cheating capability with Ca2 +, Mg2 + and other metal ions; it is biodegradable and has a strong dispersing ability and anti-redeposition ability; Daily-applied chemical detergents use it as alternative to trimer sodium phosphate for production of non-phosphorus detergent and phosphate-free liquid detergent. Adding a certain amount sodium citrate to the detergent can significantly increase the cleaning ability of detergent cleaning. The large scale of application of sodium tripolyphosphate as a builder in detergents is an important discovery in synthetic detergent industry. It is non-toxic without environmental pollution; it can also be acted as a buffer for the production of cosmetics.It can be used as Ph adjusting agents and emulsifying enhancers applied to jam, candy, jelly and ice cream; its combination with citric acid has an effect of alleviating tour; it also has effects on forming complex with metal ions. China rules that it can be applied to various types of food with appropriate usage according to the absolute necessity. It can be used as a food additive, as complex agent and buffering agent in electroplating industry; at the field of pharmaceutical industry, it is used for the manufacturing of anti-clotting drugs; and used as the detergent additives in light industry. It is used as the analysis agents used for chromatography analysis and can also used for preparing bacterial culture medium; moreover, it can also be applied into pharmaceutical industry. The product can be used for the flavoring processing of food, as stabilizers, buffers and deputy complex-forming agents in non-toxic electroplating industry; at pharmaceutical industry, it is used as anti-clotting agent, phlegm drugs and diuretics drugs. It can also be used in brewing, injection, newspaper and movies medicines.An anticoagulant also used as a biological buff. Sodium citrate is chiefly used as a food additive, usually for flavor or as a preservative. Anticoagulant for collection of blood. In photography; as sequestering agent to remove trace metals; as emulsifier, acidulant and sequestrant in foods.Sodium Citrate, Dihydrate, a conjugate base of a weak acid, can perform as a biological buffering agent because it resists changes in pH. Citric acid is one of a series of compounds responsible for the physiological oxidation of fats, carbohydrates and proteins to carbon dioxide and water. Trisodium Citrate Dihydrate is often used to prepare sodium citrate buffer for antigen retrieval of tissue samples. The citrate solution is designed to break protein cross-links; thus, unmasking antigens and epitopes in formalin-fixed and paraffin embedded tissue sections, resulting in enhancing staining intensity of antibodies. Trisodium citrate dihydrate has anticoagulant activity and as a calcium chelator, it forms complexes that disrupt the tendency of blood to clot. Molecular Weight of sodium citrate: 258.07 g/mol Hydrogen Bond Donor Count of sodium citrate: 1 Hydrogen Bond Acceptor Count of sodium citrate: 7 Rotatable Bond Count of sodium citrate: 2 Exact Mass of sodium citrate: 257.972835 g/mol Monoisotopic Mass of sodium citrate: 257.972835 g/mol Topological Polar Surface Area of sodium citrate: 141 Ų Heavy Atom Count of sodium citrate: 16 Formal Charge of sodium citrate: 0 Complexity of sodium citrate: 211 Isotope Atom Count of sodium citrate: 0 Defined Atom Stereocenter Count of sodium citrate: 0 Undefined Atom Stereocenter Count of sodium citrate: 0 Defined Bond Stereocenter Count of sodium citrate: 0 Undefined Bond Stereocenter Count of sodium citrate: 0 Covalently-Bonded Unit Count of sodium citrate: 4 Compound of sodium citrate is Canonicalized?: Yes
SODIUM COCAMINOPROPIONATE
SODIUM COCETH SULFATE Origine(s) : Végétale, Synthétique Nom INCI : SODIUM COCETH SULFATE Classification : Sulfate, Composé éthoxylé, Tensioactif anionique À SAVOIRLe sodium Coceth Sulfate est un tensioactif anionique équivalent au Sodium Laureth Sulfate. On le retrouve principalement dans certains démaquillant et produits de bain. Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM COCETH SULFATE
SODIUM COCETH-30 SULFATE N° CAS : 68891-38-3 Nom INCI : SODIUM COCETH-30 SULFATE Classification : Sulfate, Composé éthoxylé Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM COCETH-30 SULFATE
SODIUM COCO SULFOACETATE Nom INCI : SODIUM COCO SULFOACETATE 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) Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM COCO SULFOACETATE
SODIUM COCOA BUTTERATE Beurre de cacao saponifié Nom INCI : SODIUM COCOA BUTTERATE Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM COCOA BUTTERATE
SODIUM COCOAMPHOACETATE; N° CAS : 90387-76-1; Nom INCI : SODIUM COCOAMPHOACETATE; N° EINECS/ELINCS : 291-352-6/931-291-0. Classification : Tensioactif amphotère. Le sodium cocoamphoacetate est un tensioactif de type amphotère dérivé de l'huile de coco. Il est autorisé en bio. Glycine, N-(2-aminoethyl)-N-(2-hydroxyethyl)-, N-coco acyl derivs., monosodium salts
SODIUM COCOAMPHOACETATE
disodium; 2-chloroacetate;2-(4,5-dihydroimidazol-1-yl)ethanol;hydroxide; glycine, N-(2-aminoethyl)-N-(2-hydroxyethyl)-, N-coco-acyl derivatives, monosodium salts cas no: 68608-65-1
SODIUM COCOAMPHOPROPIONATE
SYNONYMS Dodecyl sodium sulfate, Dodecyl sulfate sodium salt, Lauryl sulfate sodium salt, SDS, Sodium dodecyl sulfate, Sodium lauryl sulfate CAS NO:151-21-3
SODIUM COCO-SULFATE
cas no 90170-45-9 l-Alanine; N-coco-acyl derivatives, sodium salts; Sodium N-Cocoyl-L-Alaninate; L-Alanine, N-coco acyl derivs., sodium salts;
SODIUM COCOYL ALANINATE
cas no 68187-32-6 Sodium N-Cocoyl L-Glutamate; N-Kokos-acylderivate glutamic acid, natriumsalze (German); N-coco acil derivados ácido L-glutámico, sales sódicas; (Spanish); N-acyles de coco acide L-glutamique, sels sodiques (French);
SODIUM COCOYL GLUTAMATE
Sodium cocoyl glutamate; Sodium cocoanutylglutamate cas no: 68187-32-6
SODIUM COCOYL GLUTAMINATE
cas no 29923-31-7 N-(1-Oxododecyl)-L-glicinic acid monosodium salt; N-Lauroyl-L-glicinic acid monosodium salt; Sodium N-dodecanoylglycinate; Sodium lauroyl glycinate; Monosodium N-lauroyl-L-glycinate;
SODIUM COCOYL GLYCINATE
SODIUM COCOYL GLYCINATE; N° CAS : 90387-74-9; Nom INCI : SODIUM COCOYL GLYCINATE; Nom chimique : Glycine, N-coco acyl derivs., sodium salts; N° EINECS/ELINCS : 291-350-5; Ses fonctions (INCI). Agent nettoyant : Aide à garder une surface propre. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Agent d'entretien de la peau : Maintient la peau en bon état
SODIUM COCOYL ISETHIONATE (SCI)
SODIUM COCOYL SARCOSINATE; Glycine, N-methyl-, N-coco acyl derivs, sodium salts; N° CAS : 61791-59-1, Nom INCI : SODIUM COCOYL SARCOSINATE; N° EINECS/ELINCS : 263-193-2 ; Classification : Tensioactif anionique; Ses fonctions (INCI); Agent nettoyant : Aide à garder une surface propre; Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance; Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM COCOYL SARCOSINATE
SODIUM COCOYL TAURATE N° CAS : 86089-05-6 Nom INCI : SODIUM COCOYL TAURATE N° EINECS/ELINCS : 289-173-3 Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM COCOYL TAURATE
cas no 28348-53-0 Sodium o-cumenesulfonate; Sodium 2-isopropylbenzenesulfonate; Eltesol SC 40; Benzenesulfonic acid, (1-methylethyl)-, sodium salt; Sodium Cumene Sulphonate 40;
SODIUM CUMENE SULFONATE
cumenesulfonic acid sodium salt; Sodium cumenesulphonate; SODIUM CUMENESULFONATE, N° CAS : 32073-22-6 / 28348-53-0, Nom INCI : SODIUM CUMENESULFONATE, N° EINECS/ELINCS : 250-913-5 / 248-983-7. Ses fonctions (INCI); 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 : Cumène sulfonate de sodium. Noms anglais : BENZENE, (1-METHYLETHYL)-, MONOSULFO DERIV., SODIUM SALT; CUMENESULFONIC ACID, SODIUM SALT; SODIUM CUMENE SULFONATE; 250-913-5 [EINECS]; 2-Isopropylbenzènesulfonate de sodium [French]; 32073-22-6 [RN]; Benzene, (1-methylethyl)-, monosulfo deriv., sodium salt; Benzenesulfonic acid, (1-methylethyl)-, sodium salt; benzenesulfonic acid, 2-(1-methylethyl)-, sodium salt; Benzenesulfonic acid, 2-(1-methylethyl)-, sodium salt (1:1) ; Natrium-2-isopropylbenzolsulfonat [German] ; sodium 2-(1-methylethyl)benzenesulfonate; sodium 2-(propan-2-yl)benzenesulfonate; Sodium 2-isopropylbenzenesulfonate [ACD/IUPAC Name];Sodium cumenesulphonate; SODIUM O-CUMENESULFONATE; (1-Methylethyl)benzenesulfonic acid sodium salt; CUMENE MONOSULPHO DERIVATIVE SODIUM SALT; cumene, monosulpho derivative, sodium salt; cumenesulfonic acid sodium salt; Sodium 2-(propan-2-yl) benzene sulfonate; SODIUM 2-(PROPAN-2-YL)BENZENE-1-SULFONATE; sodium 2-propan-2-ylbenzenesulfonate; Sodium 4-propan-2-ylbenzenesulfonate; Sodium cumene sulfonate; Sodium cumenesulfonate; Sodium isopropylbenzenesulfonate; SODIUM MONO-ISOPROPYLBENZENESULFONATE; Sodium-4-(1 methyl ethyl) benzene sulfonate. 250-913-5 [EINECS]; 2-Isopropylbenzènesulfonate de sodium [French] ; 32073-22-6 [RN] ; Benzene, (1-methylethyl)-, monosulfo deriv., sodium salt; Benzenesulfonic acid, (1-methylethyl)-, sodium salt; benzenesulfonic acid, 2-(1-methylethyl)-, sodium salt; Benzenesulfonic acid, 2-(1-methylethyl)-, sodium salt (1:1) [ACD/Index Name]; Natrium-2-isopropylbenzolsulfonat [German]; sodium 2-(1-methylethyl)benzenesulfonate; sodium 2-(propan-2-yl)benzenesulfonate Sodium 2-isopropylbenzenesulfonate [ACD/IUPAC Name]; Sodium cumenesulphonate; SODIUM O-CUMENESULFONATE; (1-Methylethyl)benzenesulfonic acid sodium salt; [32073-22-6] 71407-44-8 [RN]; CUMENE MONOSULPHO DERIVATIVE SODIUM SALT; cumene, monosulpho derivative, sodium salt; cumenesulfonic acid sodium salt; Sodium 2-(propan-2-yl) benzene sulfonate; SODIUM 2-(PROPAN-2-YL)BENZENE-1-SULFONATE; sodium 2-propan-2-ylbenzenesulfonate; Sodium 4-propan-2-ylbenzenesulfonate; Sodium cumene sulfonate; Sodium cumenesulfonate; Sodium isopropylbenzenesulfonate; SODIUM MONO-ISOPROPYLBENZENESULFONATE; Sodium-4-(1 methyl ethyl) benzene sulfonate; Sodium o-cumenesulfonate ; Sodium 2-isopropylbenzenesulfonate; Benzenesulfonic acid, (1-methylethyl)-, sodium salt; Sodium o-cumenesulfonate; Sodium 2-isopropylbenzenesulfonate; Benzenesulfonic acid, (1-methylethyl)-, sodium salt; 15763-77-6; Sodium o-cumenesulphonate; o-Cumenesulfonic acid, sodium salt; Sodium 2-isopropylbenzenesulphonate; o-Cumenesulphonic acid, sodium salt; SODIUM CUMENE SULFONATE; Benzenesulfonic acid, 2-(1-methylethyl)-, sodium salt (1:1); Sodium 2-(propan-2-yl) benzene sulfonate; Sodium-4-(1 methyl ethyl) benzene sulfonate; Benzene, (1-methylethyl)-, monosulfo deriv., sodium salt; Benzenesulfonic acid,(1-methylethyl)-, sodium salt (1:1) 71407-44-8
SODIUM CYANIDE
SODIUM CYANIDE (Sodyum Siyanür, SODIUM CYANIDE) Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is a poisonous compound with the formula NaCN. It is a white, water-soluble solid. Cyanide has a high affinity for metals, which leads to the high toxicity of this salt. Its main application, in gold mining, also exploits its high reactivity toward metals. It is a moderately strong base. When treated with acid, it forms the toxic gas hydrogen cyanide: NaCN + H2SO4 → HCN + NaHSO4 Contents 1 Production and chemical properties of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) 2 Applications of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) 2.1 Cyanide mining of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) 2.1.1 Sodium gold cyanide 2.2 Chemical feedstock of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) 2.3 Niche uses of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) 2.4 Homicide of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) 3 Toxicity of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) Production and chemical properties of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is produced by treating hydrogen cyanide with sodium hydroxide:[4] HCN + NaOH → NaCN + H2O Worldwide production was estimated at 500,000 tons in the year 2006. Formerly it was prepared by the Castner process involving the reaction of sodium amide with carbon at elevated temperatures. NaNH2 + C → NaCN + H2 The structure of solid NaCN is related to that of sodium chloride.[5] The anions and cations are each six-coordinate. Potassium cyanide (KCN) adopts a similar structure. Each Na+ forms pi-bonds to two CN− groups as well as two "bent" Na---CN and two "bent" Na---NC links.[6] Because the salt is derived from a weak acid, Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) readily reverts to HCN by hydrolysis; the moist solid emits small amounts of hydrogen cyanide, which smells like bitter almonds (not everyone can smell it—the ability thereof is due to a genetic trait[7]). Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) reacts rapidly with strong acids to release hydrogen cyanide. This dangerous process represents a significant risk associated with cyanide salts. It is detoxified most efficiently with hydrogen peroxide (H2O2) to produce sodium cyanate (NaOCN) and water:[4] NaCN + H2O2 → NaOCN + H2O Applications of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) Cyanide mining See also: Cyanide process Sodium gold cyanide Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is used mainly to extract gold and other precious metals in mining industry. This application exploits the high affinity of gold(I) for cyanide, which induces gold metal to oxidize and dissolve in the presence of air (oxygen) and water, producing the salt sodium gold cyanide (or gold Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE)) and sodium hydroxide: 4 Au + 8 NaCN + O2 + 2 H2O → 4 Na[Au(CN)2] + 4 NaOH A similar process uses potassium cyanide (KCN, a close relative of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE)) to produce potassium gold cyanide (KAu(CN)2). Few other methods exist for this extraction process. Chemical feedstock of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) Several commercially significant chemical compounds are derived from cyanide, including cyanuric chloride, cyanogen chloride, and many nitriles. In organic synthesis, cyanide, which is classified as a strong nucleophile, is used to prepare nitriles, which occur widely in many chemicals, including pharmaceuticals. Illustrative is the synthesis of benzyl cyanide by the reaction of benzyl chloride and Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE).[8] Niche uses of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) Being highly toxic, Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is used to kill or stun rapidly such as in widely illegal cyanide fishing and in collecting jars used by entomologists. Homicide of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) In 1986, Stella Nickell murdered her husband Bruce Nickell with Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE). In order to disguise her being responsible for the murder, she placed several bottles of Excedrin tainted with Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) on store shelves near her home in Tacoma, WA. Susan Snow, a bank manager living nearby in the same town, died several days later from taking some of the tainted Excedrin. In 1991, Joseph Meling, a resident of Tumwater, WA, copied Nickell's idea, this time tainting capsules of Sudafed on store shelves near his home to murder his wife and disguise the incident as a mass murder. Meling had forged life insurance in his wife's name totaling $700,000. Meling's wife Jennifer Meling survived the poisoning attempt but two other residents of Tumwater died after taking the tainted Sudafed. Toxicity of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) Main article: Cyanide poisoning Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE), like other soluble cyanide salts, is among the most rapidly acting of all known poisons. NaCN is a potent inhibitor of respiration, acting on mitochondrial cytochrome oxidase and hence blocking electron transport. This results in decreased oxidative metabolism and oxygen utilization. Lactic acidosis then occurs as a consequence of anaerobic metabolism. An oral dosage as small as 200–300 mg can be fatal. Aqueous solutions of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) are slightly hydrolyzed (Kh= 2.5X10-5) at ordinary temperatures to produce hydrogen cyanide. When heated in a dry carbon dioxide atmosphere, Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) fuses without much decomposition. Thermal dissociation of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) has been studied in an atm of helium at 600-1050 °C and in an atm of nitrogen at 1050-1255 °C. It has been shown that vapor phase over melt contains decomposition products. As estimated in rats given 30 mg Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) intraperitoneally over a period of 8 days, 80 percent of the total cyanide is excreted in the urine in the form of thiocyanate. The effects of carotid body chemoreceptor stimulation by Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) on respiration and phrenic nerve activity were studied in intact and vagotomized rabbits. In intact animals an intracarotid injection of 30 ug of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) resulted in an elevation of phrenic nerve activity and a rapid onset of respiratory excitation associated with an increase in respiratory rate and the response was markedly potentiated after vagotomy. The change in respiratory rate was primarily due to a decrease in expiration time in intact animals, whereas it resulted from a pronounced decrease in inspiration time in vagotomized animals. Apparently, a suppressive effect of the vagus nerve on carotid body chemoreceptor reflex occurred. An induction of a continuous increase in phrenic nerve activity accompanied by apneustic respiration by intracarotid dopamine was another evidence to support the /observation/. The major detoxification pathway for cyanide in many species is a biotransformation to the less toxic thiocyanate. Hepatic thiosulfate: cyanide sulfurtransferase (rhodanese) is the principal enzyme demonstrating in vitro catalytic activity. Despite the assumed importance of the hepatic enzyme for cyanide detoxification in vivo, the effects of liver damage (surgical or chemical) on cyanide lethality in animals have not been examined previously. Male CD-1 mice pretreated with carbon tetrachloride (CCl4, 1 mg/kg, ip 24 hr prior to the administration of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE). In other experiments carbon tetrachloride was given in the same doses at both 48 hr and 24 hr prior to Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE). Hepatotoxicity was documented by elevated serum glutamic pyruvic transaminase (SGPT) activity, by histologic evaluation of the extent of cellular necrosis, by electron microscopy of the mitochondrial fraction, and by the increased duration of zoxazolamine-induced paralysis. Lethality was not changed by carbon tetrachloride pretreatments when Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) was given alone in doses of 4 or 6 mg/kg or at a dose of 10.7 mg/kg following sodium thiosulfate (sodium sulfide, 1 g/kg, ip). A small but statistically ... protective effect was exhibited by CCl4 when Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) was given at a dose of 16 mg/kg following the administration of sodium sulfide. Rhodanese activity as measured in mitochrondrial preparations fractionated from the livers of mice pretreated with carbon tetrachloride was not different from that in animals given the corn oil vehicle even through electron micrographs showed extensive mitochondrial damage. No difference in cyanide lethality was evident between sham-operated mice and partially (2/3) hepatectomized mice at 24 hr post-surgery. An intact healthy liver does not appear to be essential for cyanide detoxification in mice whether or not thiosulfate is also given. Because rhodanese activity was slightly but ... higher in mitochondria lysed by Triton X-100 than in intact mitochondria, the mitochondrial membrane may constitute a barrier to sodium sulfide. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) releases hydrogen cyanide gas, a highly toxic chemical asphyxiant that interferes with the body’s ability to use oxygen. Exposure to Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) can be rapidly fatal. It has whole-body (systemic) effects, particularly affecting those organ systems most sensitive to low oxygen levels: the central nervous system (brain), the cardiovascular system (heart and blood vessels), and the pulmonary system (lungs). Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is used commercially for fumigation, electroplating, extracting gold and silver from ores, and chemical manufacturing. Hydrogen cyanide gas released by Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) has a distinctive bitter almond odor (others describe a musty “old sneakers smell”), but a large proportion of people cannot detect it; the odor does not provide adequate warning of hazardous concentrations. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is odorless when dry. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is shipped as pellets or briquettes. It absorbs water from air (is hygroscopic or deliquescent). Super toxic; probable oral lethal dose in humans is less than 5 mg/kg or a taste (less than 7 drops) for a 70 kg (150 lb.) person. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is poisonous and may be fatal if inhaled, swallowed or absorbed through the skin. Contact with Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) may cause burns to skin and eyes. Individuals with chronic diseases of the kidneys, respiratory tract, skin, or thyroid are at greater risk of developing toxic cyanide effects. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is not combustible itself, but contact with acids releases highly flammable hydrogen cyanide gas. Fire may produce irritating or poisonous gases. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) reacts violently with strong oxidants such as nitrates, chlorates, nitric acid, and peroxides, causing an explosion hazard. Upper and lower explosive (flammable) limits in air are not available for Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE). Cyanide is usually found joined with other chemicals to form compounds. Examples of simple cyanide compounds are hydrogen cyanide, Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) and potassium cyanide. Certain bacteria, fungi, and algae can produce cyanide, and cyanide is found in a number of foods and plants. In certain plant foods, including almonds, millet sprouts, lima beans, soy, spinach, bamboo shoots, and cassava roots (which are a major source of food in tropical countries), cyanides occur naturally as part of sugars or other naturally-occurring compounds. However, the edible parts of plants that are eaten in the United States, including tapioca which is made from cassava roots, contain relatively low amounts of cyanide. Hydrogen cyanide is a colorless gas with a faint, bitter, almondlike odor. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) and potassium cyanide are both white solids with a bitter, almond-like odor in damp air. Cyanide and hydrogen cyanide are used in electroplating, metallurgy, organic chemicals production, photographic developing, manufacture of plastics, fumigation of ships, and some mining processes. Hydrogen cyanide gas produced from Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) mixes well with air; explosive mixtures are easily formed. Warning: Heart palpitations may occur within minutes after exposure. Caution is advised. Effects may be delayed. Signs and Symptoms of Acute Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) Exposure: Signs and symptoms of acute exposure to Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) may include hypertension (high blood pressure) and tachycardia (rapid heart rate), followed by hypotension (low blood pressure) and bradycardia (slow heart rate). Cardiac arrhythmias and other cardiac abnormalities are common. Cyanosis (blue tint to the skin and mucous membranes) and cherry-red or bloody mucous membranes may occur. Tachypnea (rapid respiratory rate) may be followed by respiratory depression. Pulmonary edema and lung hemorrhage may also occur. Headache, vertigo (dizziness), agitation, and giddiness may be followed by combative behavior, dilated and unreactive pupils, convulsions, paralysis, and coma. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is irritating to the skin and mucous membranes. Lacrimation (tearing) and a burning sensation of the mouth and throat are common. Increased salivation, nausea, and vomiting are often seen. Emergency Life-Support Procedures: Acute exposure to Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) may require decontamination and life support for the victims. All exposed persons should be transported to a health care facility as quickly as possible. Emergency personnel should wear protective clothing appropriate to the type and degree of contamination. Air-purifying or supplied-air respiratory equipment should also be worn as necessary. Rescue vehicles should carry supplies such as plastic sheeting and disposable plastic bags to assist in preventing spread of contamination. Inhalation Exposure: 1. Move victims to fresh air. Emergency personnel should avoid self-exposure to Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE). 2. Evaluate vital signs including pulse and respiratory rate, and note any trauma. If no pulse is detected, provide CPR. If not breathing, provide artificial respiration. IMMEDIATELY begin administering 100% oxygen to all victims. Monitor victims for respiratory distress.Warning: To prevent self-poisoning, avoid mouth-to-mouth breathing; use a forced-oxygen mask. Direct oral contact with Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE)-contaminated persons or their gastric contents may result in self-poisoning. 3. RUSH to a health care facility! 4. Obtain authorization and/or further instructions from the local hospital for administration of an antidote or performance of other invasive procedures. Dermal/Eye Exposure: 1. Remove victims from exposure. Emergency personnel should avoid self- exposure to Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE). 2. Evaluate vital signs including pulse and respiratory rate, and note any trauma. If no pulse is detected, provide CPR. If not breathing, provide artificial respiration. IMMEDIATELY begin administering 100% oxygen to all victims. Monitor victims for respiratory distress.Warning: To prevent self-poisoning, avoid mouth-to-mouth breathing; use a forced-oxygen mask. Direct oral contact with Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE)-contaminated persons or their gastric contents may result in self-poisoning. 3. RUSH to a health care facility! 4. Remove contaminated clothing as soon as possible. 5. If eye exposure has occurred, eyes must be flushed with lukewarm water for at least 15 minutes. 6. Wash exposed skin areas twice with soap and water. 7. Obtain authorization and/or further instructions from the local hospital for administration of an antidote or performance of other invasive procedures. Ingestion Exposure: 1. Evaluate vital signs including pulse and respiratory rate, and note any trauma. If no pulse is detected, provide CPR. If not breathing, provide artificial respiration. IMMEDIATELY begin administering 100% oxygen to all victims. Monitor victims for respiratory distress.Warning: To prevent self-poisoning, avoid mouth-to-mouth breathing; use a forced-oxygen mask. Direct oral contact with Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE)-contaminated persons or their gastric contents may result in self-poisoning. 2. RUSH to a health care facility! 3. DO NOT induce vomiting. Ipecac is not recommended for ingestion of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE). 4. Obtain authorization and/or further instructions from the local hospital for administration of an antidote or performance of other invasive procedures. 5. Activated charcoal may be administered if victims are conscious and alert. Use 15 to 30 g (1/2 to 1 oz) for children, 50 to 100 g (1-3/4 to 3-1/2 oz) for adults, with 125 to 250 mL (1/2 to 1 cup) of water. 6. Promote excretion by administering a saline cathartic or sorbitol to conscious and alert victims. Children require 15 to 30 g (1/2 to 1 oz) of cathartic; 50 to 100 g (1-3/4 to 3-1/2 oz) is recommended for adults. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is non-combustible. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) releases highly flammable and toxic hydrogen cyanide gas on contact with acids or water. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is a poor candidate for incineration. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is an extremely hazardous substance (EHS) subject to reporting requirements when stored in amounts in excess of its threshold planning quantity (TPQ) of 100 lbs. Manufacturers and processors of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) are required to conduct chemical fate and terrestrial effects tests under TSCA section 4. Acute systemic toxicity of hydrogen cyanide, Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE), and potassium cyanide by instillation into the inferior conjunctival sac was investigated in rabbits. Methods of Dissemination Indoor Air: Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) can be released into indoor air as fine droplets, liquid spray (aerosol), or fine particles. Water: Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) can be used to contaminate water. Food: Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) can be used to contaminate food. Outdoor Air: Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) can be released into outdoor air as fine droplets, liquid spray (aerosol), or fine particles. Agricultural: If Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is released as fine droplets, liquid spray (aerosol), or fine particles, it has the potential to contaminate agricultural products. ROUTES OF EXPOSURE: Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) can affect the body through ingestion, inhalation, skin contact, or eye contact. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) can affect the body through ingestion, inhalation, skin contact, or eye contact. The effects of tribuyltin and Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) on hemolysis in human erythrocytes are described. Tributyltin has a sharp cut take off concentration for induction of hemolysis. A 5 uM concentration of tributyltin induces hemolysis and 1 uM or less does not in erythrocyte suspensions with lysis are sigmoidal indicating a complex molecular mechanism leading to lysis. Ten mM Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) plus 1 uM tributyltin does not stimulate hemolysis rates above levels observed with 10 mM Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) alone. Five nM Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) plus hemolytic concentrations of tributyltin stimulates hemolysis rates synergistically compared with either cyanide or tributyltin alone. Ultrastructurally, hemolytic concentrations of tribuyltin can be visualized in the electron microscope by osmium staining during fixation as electron dense spheres penetrating the lipid bilayer of the erythrocyte plasma membrane. Ten mM Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) plus 25 uM tributyltin increases slightly the size of osmiophilic structures in erythrocyte membranes compared with those spheres seen in cells exposed to 25 uM tribuyltin alone. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is the only compound tested that stimulates tributyltin induced hemolysis. CHEMICAL DANGERS: Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is water-reactive. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) decomposes on contact with acids, acid salts, water, moisture, and carbon dioxide, producing highly toxic, flammable hydrogen cyanide gas. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) solution in water is a strong base; it reacts violently with acid and is corrosive. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is incompatible with strong oxidants. Carbon dioxide from the air is sufficiently acidic to liberate toxic hydrogen cyanide gas on contact with Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE). EXPLOSION HAZARDS: Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) reacts violently with strong oxidants such as nitrates, chlorates, nitric acid, and peroxides, causing an explosion hazard. Upper and lower explosive (flammable) limits in air are not available for Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE). Containers may explode when heated or if they are contaminated with water. FIRE FIGHTING INFORMATION: Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is non-combustible. The agent itself does not burn. Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) releases highly flammable and toxic hydrogen cyanide gas on contact with acids or water. Fire will produce irritating, corrosive, and/or toxic gases. Hydrogen cyanide gas produced from Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) mixes well with air; explosive mixtures are easily formed. TIME COURSE: Effects occur rapidly following exposure to Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE). Inhalation exposure to hydrogen cyanide gas released from Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) produces symptoms within seconds to minutes; death may occur within minutes. What is Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE)? The term cyanide is clearly understood in the public consciousness to be almost synonymous with poison itself. This is largely because of its use as lethal suicide pill (L-pill) in World War 2, most notably with the suicide of Nazi army officer Erwin Rommel. The cyanide used in the L-pill was potassium cyanide but the properties of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) are nearly identical. An inorganic and very innocent looking white solid with deadly properties, Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) (NaCN) can be fatal at amounts as little as 5% of a teaspoon. It is produced from the equally dangerous gas hydrogen cyanide (HCN) in a simple process with sodium hydroxide. Why would a company want so much of it? Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is used industrially across the globe, most frequently in the mining of gold. Although most of us have the traditional imagery of a 19th-century gold miner panning for nuggets, this isn’t the industrial method used today. After mining and milling, the crude rock mixture is turned into a fine powder and added to a solution of Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE). The gold forms strong bonds with cyanide molecules and can then be separated from the rest of the minerals because it is then soluble in water. It then reacts with zinc and turns back into a solid. Finally is smelted to isolate the gold and cast into bars. How dangerous is it? As with the very similar potassium cyanide used in the L-pill, Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is extremely toxic to humans. Although there are risks with skin absorption, the biggest risk is ingestion. Inhaling or swallowing Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) blocks oxygen transport causing serious medical problems and ultimately death. Gold Extraction Process Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) has been used in the extraction of gold from ore for over a century. Today it is still considered the most efficient extraction method – with Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) used in the leaching process in most gold mining operations. Solid Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is produced to form a white crystalline briquette or ‘cyanoid’. Liquid Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) is delivered to mine sites via purpose-built isotanks that are suitable for road or rail transport. In inorganic cyanides, the cyanide group is present as the anion CN−. Salts such as Sodium cyanide (Sodyum Siyanür, SODIUM CYANIDE) and potassium cyanide are highly toxic.[2] Hydrocyanic acid, also known as hydrogen cyanide, or HCN, is a highly volatile liquid that is produced on a large scale industrially. It is obtained by acidification of cyanide salts.
SODIUM DECYL SULFATE ( Sulfate de sodium et de décyle)
SODIUM DEHYDROACETATE, N° CAS : 4418-26-2 - Déhydroacétate de sodium. sodium dehydracetate; Sodium dehydroacetate; Origine(s) : Synthétique. Autre langue : Dihidroacetato sódico, Nom INCI : SODIUM DEHYDROACETATE. Nom chimique : Sodium 1-(3,4-dihydro-6-methyl-2,4-dioxo-2H-pyran-3-ylidene)ethanolate; N° EINECS/ELINCS : 224-580-1 Additif alimentaire : E266. Le déhydroacétate de sodium est un conservateur utilisé dans les cosmétiques pour ses propriétés antimicrobiennes. Même si l'ingrédient semble poser peu de problèmes pour la santé, notez toutefois que sa concentration est limitée (voir ci-dessous) et qu'il est interdit dans les produits en spray de type aérosol. Il est autorisé en Bio.Ses fonctions (INCI) Conservateur : Inhibe le développement des micro-organismes dans les produits cosmétiques. Classification : Règlementé, Conservateur. Sodium 1-(3,4-dihydro-6-methyl-2,4-dioxo-2H-pyran-3-ylidene)ethanolate; sodium 1-(3,4-dihydro-6-methyl-2,4-dioxo-2H-pyran-3-ylidene)ethonolate; sodium 1-(3,4-dihydro-6-methyl-2,4-dioxo-2H-pyran-3-ylidene)ethonolate; sodium dehydracetate; sodium dehydracetate; Sodium dehydroacetate. Translated names: 1-(3,4-dihidro-6-metil-2,4-dioxo-2H-piran-3-iliden)etanolato de sodio (es); 1-(3,4-dihydro-6-méthyl-2,4-dioxo-2H-pyranne-3-ylidène)éthanolate de sodium (fr); 1-(3,4-diidro-6-metil-2,4-diosso-2H-piran-3-iliden)etanolato di sodio (it); 1-(3,4-diidro-6-metil-2,4-dioxo-2H-pirano-3-ilideno)etanolato de sódio (pt); 1-(3,4-διυδρο-6-μεθυλο-2,4-διοξο-2H-πυραν-3-υλιδεν)αιθυλικό νάτριο (el); 3-acetyl-6-methyltetrahydropyran-2,4-dion, sodná sůl (cs); 3-acetylo-6-metylo-4-okso-4H-piran-2-olan sodu (pl); dehidracetato de sódio (pt); dehidracetato sódico (es); dehydracetová kyselina, sodná sůl (cs); dehydrooctan sodu (pl); deidracetato di sodio (it); déhydroacétate de sodium (fr); Naatrium-1-(3,4-dihüdro-6-metüül-2,4-diokso-2H-püraan-3-ülideen)etonolaat (et); Naatriumdehüdroatsetaat (et); natrijev 1-(3,4-dihidro-6-metil-2,4-diokso-2H-piran-3-iliden)etonolat (hr); natrijev 1-(3,4-dihidro-6-metil-2,4-diokso-2H-piran-3-iliden)etanolat (sl); natrijev dehidracetat (hr); natrijev dehidroacetat (sl) ; natrio 1-(3,4-dihidro-6-metil-2,4-diokso-2H-piran-3-iliden)etanoliatas (lt); natrio dehidracetatas (lt); natrium dehydracetaat (nl); natrium dehydracetat (da); natrium-1-(3,4-dihydro-6-methyl-2,4-dioxo-2H-pyran-3-ylideen)ethanolaat (nl); natrium-1-(3,4-dihydro-6-methyl-2,4-dioxo-2H-pyran-3-yliden)ethanolat (da); natrium-1-(3,4-dihydro-6-metyl-2,4-diokso-2H-pyran-3-yliden)etanolat (no); natrium-1-(3,4-dihydro-6-metyl-2,4-dioxo-2H-pyran-3-yliden)etanolat (sv); natriumdehydracetat (no); Natriumdehydroasetaatti (fi); nátrium-1-(3,4-dihidro-6-metil-2,4-dioxo-2H-pirán-3-Ilidén)-etanolát (hu); nátrium-3-acetyl-4-oxo-6-metyl-4H-pyrán-2-olát (sk); nátrium-dehidracetát (hu); nātrija 1-(3,4-dihidro-6-metil-2,4-diokso-2H-pirān-3-ilidēn)etonolāts (lv); nātrija dehidracetāts (lv) ; sodiu 1-(3,4-dihidro-6-metil-2,4-dioxo-2H-piran-3-iliden)etonolat (ro); sodiu dehidracetat (ro); δεϋδροξικό νάτριο (el); натриев дехидрацетат (bg); натриев-1-(3,4-дихидро-6-метил-2,4-диоксо-2H-пиран-3-илиден)eтанолат (bg) CAS names 2H-Pyran-2,4(3H)-dione, 3-acetyl-6-methyl-, ion(1-), sodium (1:1) 1-(3,4-dihydro-6-methyl-2,4-dioxo-2H-pyran-3-ylidene)ethanolate sodium sodium (1E)-1-(6-methyl-2,4-dioxopyran-3-ylidene)ethanolate sodium 1-(3,4-dihydro-6methyl-2,4-dioxo-2H-pyran-3ylidene)ethanolate sodium 1-(6-methyl-2,4-dioxo-2H-pyran-3(4H)-ylidene)ethanolate sodium 1-(6-methyl-2,4-dioxo-pyran-3-ylidene)ethanolate sodium 3-acetyl-6-methylpyran-3-ide-2,4-dione Sodium dehydracetate, Dehydroacetic acid sodium salt, 3-(1-Hydroxyethylidene)-6-methyl-2H-pyran-2,4(3H)-dione sodium salt; 1-(6-Méthyl-2,4-dioxo-2H-pyran-3(4H)-ylidène)éthanolate de sodium [French] [ACD/IUPAC Name] 224-580-1 [EINECS] 2H-Pyran-2,4(3H)-dione, 3-(1-hydroxyethylidene)-6-methyl-, sodium salt (1:1) [ACD/Index Name] 4418-26-2 [RN] Natrium-1-(6-methyl-2,4-dioxo-2H-pyran-3(4H)-yliden)ethanolat [German] [ACD/IUPAC Name] Sodium 1-(6-methyl-2,4-dioxo-2H-pyran-3(4H)-ylidene)ethanolate [ACD/IUPAC Name] Sodium dehydroacetate Sodium 1-(3,4-dihydro-6-methyl-2,4-dioxo-2H-pyran-3-ylidene)ethanolate
SODIUM DEHYDROACETATE ( Déhydroacétate de sodium)
cas no 7789-12-0 Dichromic acid disodium aalt dihydrate; Sodium dichromate dihydrate; Disodium dichromate dihydrate; Sodium dichromate; Natriumdichromat (German); Dicromato de sodio (Spanish); Dichromate de sodium (French); Sodio (dicromato di) (Italian);
SODIUM DIETHYLHEXYL SULFOSUCCINATE
SODIUM DILAURETH-7 CITRATE, Nom INCI : SODIUM DILAURETH-7 CITRATE. Classification : Composé éthoxylé. 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). Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM DILAURETH-7 CITRATE
cas no 128-04-1 Sodium dimethyldithiocarbamate; Carbam-S; SDDC; Dimethyldithiocarbamate sodium salt; Dimethyldithiocarbamic acid sodium salt; Methyl namate; N,N-Dimethyldithiocarbamate sodium salt; N,N-Dimethyldithiocarbamic acid sodium salt; Sodam; Sodium N,N-dimethyldithiocarbamate; Sodium dimethyl dithiocarbamate; Sodium dimethylaminecarbodithioate; Sodium dimethylaminocarbodithioate; Sodium dimethylcarbamodithioate; Sodium dimethyldithiocarbamate; Thiostop N;
SODIUM DIMETHYLDITHIOCARBAMATE
SODIUM DIMETHYLDITHIOCARBAMATE Dimethyldithiocarbamate Chemical structure of the dimethyldithiocarbamate anion Dimethyldithiocarbamate is the organosulfur anion with the formula (CH3)2NCS2−. It is one of the simplest organic dithiocarbamate. Uses It is a component of various pesticides and rubber chemicals in the form of its salts sodium dimethyldithiocarbamate, and potassium dimethyldithiocarbamate) as well as its complexes zinc dimethyldithiocarbamate, ferric dimethyldithiocarbamate, and nickel bis(dimethyldithiocarbamate). Oxidation gives thiram. Properties Related Categories Building Blocks, Chemical Synthesis, Organic Building Blocks, Sulfur Compounds, Thiocarbonyl Compounds Molecular Weight of Sodium dimethyldithiocarbamate: 143.21 g/mol Computed by PubChem 2.1 (PubChem release 2019.06.18) Hydrogen Bond Donor Count of Sodium dimethyldithiocarbamate: 0 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Hydrogen Bond Acceptor Count of Sodium dimethyldithiocarbamate: 2 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Rotatable Bond Count of Sodium dimethyldithiocarbamate: 0 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Exact Mass of Sodium dimethyldithiocarbamate: 142.983936 g/mol Computed by PubChem 2.1 (PubChem release 2019.06.18) Monoisotopic Mass of Sodium dimethyldithiocarbamate: 142.983936 g/mol Computed by PubChem 2.1 (PubChem release 2019.06.18) Topological Polar Surface Area of Sodium dimethyldithiocarbamate: 36.3 Ų Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Heavy Atom Count of Sodium dimethyldithiocarbamate: 7 Computed by PubChem Formal Charge of Sodium dimethyldithiocarbamate: 0 Computed by PubChem Complexity of Sodium dimethyldithiocarbamate: 64 Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18) Isotope Atom Count of Sodium dimethyldithiocarbamate: 0 Computed by PubChem Defined Atom Stereocenter Count of Sodium dimethyldithiocarbamate: 0 Computed by PubChem Undefined Atom Stereocenter Count of Sodium dimethyldithiocarbamate: 0 Computed by PubChem Defined Bond Stereocenter Count of Sodium dimethyldithiocarbamate: 0 Computed by PubChem Undefined Bond Stereocenter Count of Sodium dimethyldithiocarbamate: 0 Computed by PubChem Covalently-Bonded Unit Count of Sodium dimethyldithiocarbamate: 2 Computed by PubChem Compound of Sodium dimethyldithiocarbamate Is Canonicalized Yes Sodium dimethyldithiocarbamate act as materials preservatives for fuels, metalworking fluids, paints, coatings, adhesives, cloth, and paper/paperboard; they act as antifoulants/slimicides in a variety of liquids including industrial/commercial cooling water, air washer water, sugar mill pulp/process water, marine heat exchangers, gas/oil recovery fluid, industrial wastewater treatment systems, industrial water purification systems, reverse osmosis water systems, and pasteurizer cooling water. Their main uses are as antifoulants in industrial cooling and air washer water systems, as well as pulp and paper mills and gas/oil drilling muds. Product description SDDC (Sodium Dimethyldithiocarbamate) is a yellowish aqueous solution and is used in the following applications: Biocide for paper mills, sugar mills, water treatment, leather industry Heavy metal scavenger Applications/uses Water treatment industrial . Sodium dimethyldithiocarbamate, is used to aid the precipitation of metals in industrial wastewater treatment and pretreatment systems. When used appropriately it can effectively enhance the removal of some difficult to treat pollutants, without impacting the environment or POTW operations. However, sodium dimethyldithiocarbamate is toxic to aquatic life and can combine to form, or break down to, a number of other toxic chemicals, including thiram (an EPA registered fungicide) and other thiurams, other dithiocarbamates, carbon disulfide, and dimethylamine. Thiram is known to be toxic to aquatic life at the following levels: LC50 less than 10 :g/l (parts per billion) including some less than 1 :g/l for several varieties of catfish, carp, rainbow trout, daphnia, and harlequinfish; LC50 between 10 and 100 ug/l in other studies Occurence(s)/Use(s) Herbicide, biocide (cutting oils and aqueous systems), coagulant, vulcanizing agent, chelating agent; water treatment (precipitate heavy metal ions); stops polymerization of synthetic latexes in rubber Sodium dimethyldithiocarbamate Agent Name Sodium dimethyldithiocarbamate CAS Number 128-04-1 Formula C3-H6-N-S2.Na Major Category Pesticides Sodium dimethyldithiocarbamate formula graphical representation Synonyms Aceto SDD 40; Alcobam NM; Amersep MP 3R; Brogdex 555; Carbam S; Carbam-S; DDC; DMDK; Diaprosim AB 13; Dibam; Dibam A; Dimethyldithiocarbamate sodium salt; Dimethyldithiocarbamic acid, sodium salt; Diram; MSL; MSL (carbamate); MetalPlex 143; Methyl namate; N,N-Dimethyldithiocarbamate sodium salt; N,N-Dimethyldithiocarbamic acid, sodium salt; Nalmet A 1; Nocceler S; SDDC; Sanceler S; Sdmdtc; Sharstop 204; Sodam; Sodium N,N-dimethyldithiocarbamate; Sodium dimethyl dithiocarbamate; Sodium dimethylaminecarbodithioate; Sodium dimethylaminocarbodithioate; Sodium dimethylcarbamodithioate; Sta-Fresh 615; Steriseal liquid #40; Thiostop N; Vinditat; Vinstop; Vulnopol NM; Wing Stop B; Carbamic acid, dimethyldithio-, sodium salt; [ChemIDplus] Category Dithiocarbamates (Pesticide) Description 40% aqueous solution: Yellow liquid; [HSDB] Off-white to cream colored flakes; [MSDSonline] Sources/Uses Used as a disinfectant, corrosion inhibitor, coagulant, vulcanizing agent, chelating agent, fungicide, and biocide (paints, cutting oils, water treatment, leather tanning, and paper manufacturing); [HSDB] Comments May cause irritation; [MSDSonline] Several of the dialkyldithiocarbamates are known skin sensitizers.
SODIUM DIOCTYL SULFOSUCCINATE
Sodium dodecylbenzene sulfonate. Utilisation et sources d'émission: Agent nettoyant, agent dispersant; Sodium dodecylbenzenesulfonate. CAS names; Benzenesulfonic acid, dodecyl-, sodium salt (1:1); SODIUM DODECYLBENZENESULFONATE, N° CAS : 25155-30-0, Nom INCI : SODIUM DODECYLBENZENESULFONATE, Nom chimique : Sodium dodecylbenzenesulphonate. N° EINECS/ELINCS : 246-680-4. Classification : Tensioactif anionique. 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).Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : BENZENESULFONIC ACID, DODECYL-, SODIUM SALT; DODECYL BENZENE SULFONATE DE SODIUM; DODECYL BENZENESULFONIC ACID, SODIUM SALT; DODECYLBENZENE SULFONATE DE SODIUM; DODECYLBENZENESULFONATE DE SODIUM; DODECYLBENZENESULFONIC ACID SODIUM SALT; Dodécylbenzènesulfonate de sodium; Sel de sodium de l'acide dodécylbenzènesulfonique; SEL SODIQUE DE L'ACIDE DODECYLBENZENESULFONIQUE; SODIUM DODECYL BENZENE SULFONATE; Sodium dodecylbenzene sulfonate; Sodium dodecylbenzenesulfonate; SODIUM LAURYLBENZENESULFONATE; SODIUM, DODECYL BENZENE SULFONATE DE ; SODIUM, DODECYLBENZENE SULFONATE DE; SODIUM, DODECYLBENZENESULFONATE DE. Noms anglais : Sodium dodecylbenzene sulfonate. Utilisation et sources d'émission: Agent nettoyant, agent dispersant; Sodium dodecylbenzenesulfonate. CAS names; Benzenesulfonic acid, dodecyl-, sodium salt (1:1); : alkylarylsulphonates; Benzenesulfonic acid, dodecyl-, sodium salt; Dodecene-1 LAS (JIS K 3363-1990) ; Dodecylbenzene sulfonic acid, sodium salt; DUBAROL; sodium 2-dodecylbenzene-1-sulfonate; SODIUM 2-DODECYLBENZENESULFONATE; Sodium 4-dodecylbenzenesulfonate; Sodium dodecyl benzene sulfonate; sodium dodecyl benzenesulfonate; sodium dodecylbenzenesufonate; Sodium Dodecylbenzenesulfonate (Sodium Alkylbenzenesulfonate C10-C13); Sodium dodecylbenzenesulphonate; Sodiumdodecylbenzenesulfonate; Tetrapropylenbenzenesulfonic acid sodium salt ; Trade names: Alkyl(C12)benzenesulfonic acid, sodium salt; Dodecylbenzene sodium sulfonate; dodecylbenzenesulfonic acid, sodium salt; Na-C12 LAS; SDBS; Sodium Dodecyl Benzene Sulphonate; sodium dodecylbenzene sulphonate; Sodium laurylbenzenesulfonate; sodium linear C12 Alkylbenzene sulfonate; Sodium 4-dodecylbenzenesulfonate [ACD/IUPAC Name] ; 218-654-2 [EINECS]; 25155-30-0 [RN]; 4171051; 4-Dodécylbenzènesulfonate de sodium [French] ; 4-Dodecylbenzenesulfonic acid, sodium salt; benzenesulfonic acid, 4-dodecyl-, sodium salt ; Benzenesulfonic acid, 4-dodecyl-, sodium salt (1:1) [ACD/Index Name]; DB6825000; MFCD00011508; Natrium-4-dodecylbenzolsulfonat [German] [ACD/IUPAC Name]; SDBS; sodium 4-dodecylbenzenesulphonate; sodium dodecyl benzenesulfonate; sodium dodecylbenzenesulfonate; sodium para-dodecylbenzene sulfonate; SODIUM P-DODECYLBENZENESULFONATE ; 11067-82-6 [RN]; 4-(2-dodecyl)benzene sulfonate sodium salt; Benzenesulfonic acid,4-dodecyl-, sodium salt (1:1); Dodecyl benzenesulfonic acid, sodium salt; DODECYLBENZENESODIUMSULFONATE; EINECS 218-654-2; P-DODECYLBENZENESULFONIC ACID, SODIUM SALT; sodium 4-dodecylbenzene-1-sulfonate; sodium 4-laurylbenzenesulfonate
SODIUM DODECYL SULFATE
CAS Number: 151-21-3
IUPAC name: Sodium dodecyl sulfate
Chemical formula: C12H25NaSO4
Molar mass: 288.372 g
EC Number: 205-788-1

Sodium dodecyl sulfate (SDS) or Sodium dodecyl sulfate (SLS), sometimes written sodium laurilsulfate, is an organic compound with the formula CH3(CH2)11OSO3Na.
Sodium dodecyl sulfate is an anionic surfactant used in many cleaning and hygiene products.
This compound is the sodium salt of the 12-carbon an organosulfate.
Sodium dodecyl sulfates hydrocarbon tail combined with a polar "headgroup" give the compound amphiphilic properties and so make it useful as a detergent.
Sodium dodecyl sulfate is also component of mixtures produced from inexpensive coconut and palm oils.
Sodium dodecyl sulfate is a common component of many domestic cleaning, personal hygiene and cosmetic, pharmaceutical,
and food products, as well as of industrial and commercial cleaning and product formulations.

Physicochemical properties
The critical micelle concentration (CMC) in water at 25 °C is 8.2 mM, and the aggregation number at this concentration is usually considered to be about 62.
The micelle ionization fraction (α) is around 0.3 (or 30%).

Applications
Cleaning and hygiene
Sodium dodecyl sulfate is mainly used in detergents for laundry with many cleaning applications.
Sodium dodecyl sulfate is a highly effective surfactant and is used in any task requiring the removal of oily stains and residues. For example, it is found in higher concentrations with industrial products including engine degreasers, floor cleaners, and car exterior cleaners.

Sodium dodecyl sulfate is a component in hand soap, toothpastes, shampoos, shaving creams, and bubble bath formulations, for its ability to create a foam (lather), for its surfactant properties, and in part for its thickening effect.

Food additive
Sodium dodecyl sulfate, appearing as its synonym Sodium dodecyl sulfate (SLS), is considered a generally recognized as safe (GRAS) ingredient for food use according to the USFDA (21 CFR 172.822).


Sodium dodecyl sulfate is used as an emulsifying agent and whipping aid.
As an emulsifier in or with egg whites the United States Code of Federal Regulations require that it must not exceed 1,000 parts per million (0.1%) in egg white solids or 125 parts per million (0.0125%) in frozen or liquid egg whites and as a whipping agent for the preparation of marshmallows it must not exceed 0.5% of the weight of gelatine.
SLS is reported to temporarily diminish perception of sweetness.

Laboratory applications
Sodium dodecyl sulfate is used in cleaning procedures, and is commonly used as a component for lysing cells during RNA extraction and/or DNA extraction, and for denaturing proteins in preparation for electrophoresis in the Sodium dodecyl sulfate-PAGE technique.


Denaturation of a protein using Sodium dodecyl sulfate
In the case of Sodium dodecyl sulfate-PAGE, the compound works by disrupting non-covalent bonds in the proteins, and so denaturing them, i.e. causing the protein molecules to lose their native conformations and shapes.

By binding to proteins at a ratio of one Sodium dodecyl sulfate molecule per 2 amino acid residues, the negatively charged detergent provides all proteins with a similar net negative charge and therefore a similar charge-to-mass ratio.
In this way, the difference in mobility of the polypeptide chains in the gel can be attributed solely to their length as opposed to both their native charge and shape.

Sodium dodecyl sulfate is possible to make separation based on the size of the polypeptide chain to simplify the analysis of protein molecules, this can be achieved by denaturing proteins with the detergent Sodium dodecyl sulfate.

Pharma applications
Sodium dodecyl sulfate is a widely used in the pharmaceutical field as an ionic solubilizer and emulsifier that is suitable for applications in liquid dispersions, solutions, emulsions and micro emulsions, tablets, foams and semi-solids such as creams, lotions and gels.

Additionally, SLS aids in tablet wettability, as well as lubrication during manufacturing. Brand names of pharma-grade SLS include Kolliphor SLS and Kolliphor SLS Fine.

Miscellaneous applications
SLS is used in an improved technique for preparing brain tissues for study by optical microscopy.
The technique, which has been branded as CLARSodium dodecyl sulfate, was the work of Karl Deisseroth and coworkers at Stanford University, and involves infusion of the organ with an acrylamide solution to bind the macromolecules of the organ (proteins, nucleic acids, etc.), followed by thermal polymerization to form a "brain–hydrogel" (a mesh interspersed throughout the tissue to fix the macromolecules and other structures in space), and then by lipid removal using Sodium dodecyl sulfate to eliminate light scattering with minimal protein loss, rendering the tissue quasi-transparent.

Along with sodium dodecylbenzene sulfonate and Triton X-100, aqueous solutions of Sodium dodecyl sulfate are popular for dispersing or suspending nanotubes, such as carbon nanotubes.

Niche uses
SLS has been proposed as a potentially effective topical microbicide, for intravaginal use, to inhibit and possibly prevent infection by various enveloped and non-enveloped viruses such as the herpes simplex viruses, HIV, and the Semliki Forest virus.

Liquid membranes formed from Sodium dodecyl sulfate in water have been demonstrated to work as unusual particle separators.
The device acts as a reverse filter, allowing large particles to pass while capturing smaller particles.

Production
Sodium dodecyl sulfate is synthesized by treating lauryl alcohol with sulfur trioxide, oleum, or chlorosulfuric acid to produce hydrogen lauryl sulfate.
Lauryl alcohol can be used in pure form or as a mixtures of fatty alcohols.

When produced from these sources, "Sodium dodecyl sulfate" products are a mixture of various sodium alkyl sulfates with Sodium dodecyl sulfate being the main component.
For instance, Sodium dodecyl sulfate is a component, along with other chain-length amphiphiles, when produced from coconut oil, and is known as sodium coco sulfate (SCS).

Sodium dodecyl sulfate is available commercially in powder, pellet, and other forms (each differing in rates of dissolution), as well as in aqueous solutions of varying concentrations.

Safety
Sodium dodecyl sulfate is not carcinogenic.
Like all detergents, Sodium dodecyl sulfate removes oils from the skin, and can cause skin and eye irritation.
Sodium dodecyl sulfate has been shown to irritate the skin of the face, with prolonged and constant exposure (more than an hour) in young adults.
Sodium dodecyl sulfate may worsen skin problems in individuals with chronic skin hypersensitivity, with some people being affected more than others.

Oral concerns
The low cost of Sodium dodecyl sulfate, its lack of impact on taste, its potential impact on volatile sulfur compounds (VSCs), which contribute to malodorous breath, and its desirable action as a foaming agent have led to the use of Sodium dodecyl sulfate in the formulations of toothpastes.

A series of small crossover studies (25–34 patients) have supported the efficacy of SLS in the reduction of VSCs, and its related positive impact on breath malodor, although these studies have been generally noted to reflect technical challenges in the control of study design variables.

While primary sources from the group of Irma Rantanen at University of Turku, Finland conclude an impact on dry mouth (xerostomia) from SLS-containing pastes, a 2011 Cochrane review of these studies, and of the more general area, concludes that there "is no strong evidence… that any topical therapy is effective for relieving the symptom of dry mouth".

A safety concern has been raised on the basis of several studies regarding the effect of toothpaste Sodium dodecyl sulfate on aphthous ulcers, commonly referred to as canker or white sores.
A consensus regarding practice (or change in practice) has not appeared as a result of the studies.

As Lippert notes, of 2013, "very few… marketed toothpastes contain a surfactant other than Sodium dodecyl sulfate," and leading manufacturers continue to formulate their produce with Sodium dodecyl sulfate.

Appearance: White or cream-colored crystals, flakes, or powder
Odor: Faint odor of fatty substances
Density: 1.01 g/cm3
Melting point: 206 °c
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 12
Exact Mass: 288.13712473
Monoisotopic Mass: 288.13712473
Topological Polar Surface Area: 74.8 Ų
Heavy Atom Count: 18
Complexity: 249
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 2
Compound Is Canonicalized: Yes

About Sodium dodecyl sulfate
Sodium dodecyl sulfate is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 to < 100 000 tonnes per annum.

Sodium dodecyl sulfate is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.

Consumer Uses of Sodium dodecyl sulfate
Sodium dodecyl sulfate is used in the following products: washing & cleaning products, coating products, plant protection products, adhesives and sealants, fillers, putties, plasters, modelling clay, air care products, polishes and waxes and cosmetics and personal care products.

Other release to the environment of Sodium dodecyl sulfate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).

Article service life of Sodium dodecyl sulfate
Other release to the environment of Sodium dodecyl sulfate is likely to occur from: indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment) and outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials). Sodium dodecyl sulfate can be found in complex articles, with no release intended: vehicles and machinery, mechanical appliances and electrical/electronic products (e.g. computers, cameras, lamps, refrigerators, washing machines). Sodium dodecyl sulfate can be found in products with material based on: plastic (e.g. food packaging and storage, toys, mobile phones) and paper (e.g. tissues, feminine hygiene products, nappies, books, magazines, wallpaper).

Widespread uses by professional workers
Sodium dodecyl sulfate is used in the following products: adhesives and sealants, coating products, fillers, putties, plasters, modelling clay, plant protection products and polymers.
Sodium dodecyl sulfate is used in the following areas: building & construction work and agriculture, forestry and fishing.

Other release to the environment of Sodium dodecyl sulfate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.

Formulation or re-packing of Sodium dodecyl sulfate
Sodium dodecyl sulfate is used in the following products: cosmetics and personal care products, washing & cleaning products, air care products, biocides (e.g. disinfectants, pest control products), coating products, fillers, putties, plasters, modelling clay, polishes and waxes and polymers.
Release to the environment of Sodium dodecyl sulfate can occur from industrial use: formulation of mixtures.

Uses of Sodium dodecyl sulfate at industrial sites
Sodium dodecyl sulfate is used in the following products: polymers, laboratory chemicals, biocides (e.g. disinfectants, pest control products), metal surface treatment products, pH regulators and water treatment products and washing & cleaning products.

Sodium dodecyl sulfate is used in the following areas: building & construction work.
Sodium dodecyl sulfate is used for the manufacture of: plastic products, chemicals and rubber products.

Release to the environment of Sodium dodecyl sulfate can occur from industrial use: in processing aids at industrial sites, in the production of articles, as an intermediate step in further manufacturing of another substance (use of intermediates), as processing aid and for thermoplastic manufacture.

Other release to the environment of Sodium dodecyl sulfate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.

Sodium dodecyl sulfate (SLS) is an anionic surfactant naturally derived from coconut and/or palm kernel oil.
Sodium dodecyl sulfate usually consists of a mixture of sodium alkyl sulfates, mainly the lauryl.

Sodium dodecyl sulfate lowers surface tension of aqueous solutions and is used as fat emulsifier, wetting agent, and detergent in cosmetics, pharmaceuticals and toothpastes.
Sodium dodecyl sulfate is also used in creams and pastes to properly disperse the ingredients and as research tool in protein biochemistry. SLS also has some microbicidal activity.

Sodium dodecyl sulfate is used as a surfactant in shampoos and toothpastes.
Sodium dodecyl sulfate also has microbicidal activities against both enveloped (Herpes simplex viruses, HIV-1, Semliki Forest virus) and nonenveloped (papillomaviruses, reovirus, rotavirus and poliovirus) viruses, although it has not been approved for this use.

Like other surfactants, Sodium dodecyl sulfate is amphiphilic.
Sodium dodecyl sulfate thus migrates to the surface of liquids, where its alignment and aggregation with other Sodium dodecyl sulfate molecules lowers the surface tension. This allows for easier spreading and mixing of the liquid.
Sodium dodecyl sulfate has potent protein denaturing activity and inhibits the infectivity of viruses by by solubilizing the viral envelope and/or by denaturing envelope and/or capsid proteins.

Sodium dodecyl sulfate is an organic sodium salt that is the sodium salt of dodecyl hydrogen sulfate. Sodium dodecyl sulfate has a role as a detergent and a protein denaturant.

Dodecyl sulfate, [sodium salt] appears as white to pale yellow paste or liquid with a mild odor.
Sinks and mixes with water. (USCG, 1999)

An anionic surfactant, usually a mixture of sodium alkyl sulfates, mainly the lauryl; lowers surface tension of aqueous solutions; used as fat emulsifier, wetting agent, detergent in cosmetics, pharmaceuticals and toothpastes; also as research tool in protein biochemistry.

Features of Sodium Dodecyl Sulfate (Lauryl):
Popular anionic detergent for a variety of protein methods Especially useful for denaturing polyacrylamide gel electrophoresis (SDS-PAGE)
Common component of cell lysis buffers

This lauryl-grade sodium dodecyl sulfate (SDS) is a popular anionic detergent for routine protein electrophoresis and cell lysis methods. The formulation is a mixture of several different alkyl sulfate chain lengths (C10 to C18).

Sodium dodecyl sulfate (sodium lauryl sulfate) also called SDS (= sodium dodecyl sulfate), is an anionic surfactant that is used as a detergent, eg. in detergents or toothpaste.
Sodium dodecyl sulfate is also used as a denaturant for proteins, and is mainly used in biochemistry and biotechnology.
The effect on proteins is based on breaking non-covalent bonds of the proteins and thus destroying their quaternary and tertiary structure.

Sodium Dodecyl Sulfate (SDS) is an anionic detergent that denatures secondary and nondisulfide-linked tertiary protein structure, shattering the native shape.
Sodium Dodecyl Sulfate provides a negative charge to each protein as a function of their size.

Accordingly, all of proteins have the same shape in the gel separation they are separated only for their size. Furthermore, Sodium Dodecyl Sulfate can be used to aid in lysing cell during DNA extraction.

Sodium Dodecyl Sulfate is what’s known as a “surfactant”.
This means it lowers the surface tension between ingredients, which is why it’s used as a cleansing and foaming agent.

Most concerns about Sodium Dodecyl Sulfate stem from the fact that it can be found in beauty and self-care products as well as in household cleaners.

Grooming products, such as shaving cream, lip balm, hand sanitizer, nail treatments, makeup remover, foundation, facial cleansers, exfoliants, and liquid hand soap

Hair products, such as shampoo, conditioner, hair dye, dandruff treatment, and styling gel

Dental care products, such as toothpaste, teeth whitening products, and mouthwash

Bath products, such as bath oils or salts, body wash, and bubble bath

Creams and lotions, such as hand cream, masks, anti-itch creams, hair-removal products, and sunscreen

Sodium Dodecyl Sulfate (SDS) is a surfactant, which basically means it has an effect on the surfaces it touches. It’s used in a variety of products such as food thickeners, toothpaste, and floor cleaners.

Uses of Sodium Dodecyl Sulfate
All the soaps and cleaning products that you use are a mix of water and oil.
But they don’t mix together on their own.

Instead, surfactants bring them together.
Soap's cleaning power comes from the bonded oil and water molecules rubbing against dirt and grease.

That is why so many products have surfactants in them.
They blend the ingredients that make cleaning happen.‌

Sodium lauryl sulfate is very easy and inexpensive to make, and it works well in many situations. You'll see it listed as an ingredient in common products found in the home and in the workplace. ‌

Personal Products. These include things like:

Body wash
Hand soap
Facial cleaner
Bubble bath
Toothpaste
Shampoo

Sodium Dodecyl Sulfate is also a foaming agent.
Many of these products use Sodium Dodecyl Sulfate to give a foaming action during the cleaning process.
If you have a foaming face wash or are working up a good lather with your shampoo, you're probably using something with SLS.‌

Sodium Dodecyl Sulfate’s ability to break down oil and grease lends itself well to industrial products.
You can find it in household cleaning products as well as engine cleaners and industrial-strength soaps. ‌

You may see Sodium Dodecyl Sulfate used in certain foods you eat, within limits approved by the FDA.
As a food additive, SLS can make marshmallows fluffier and dried egg products lighter.
Sodium Dodecyl Sulfate helps mix citrus and other acidic liquids with water to make fruit drinks.

Sodium Dodecyl Sulfate (SDS), also known as Sodium lauryl sulfate, is a widely used surfactant in cleaning products, cosmetics, and personal care products.
The sodiumclauryl sulfate formula is a highly effective anionic surfactant used to remove oily stains and residues.

Sodium Dodecyl Sulfate is found in high concentrations in industrial products, including engine degreasers, floor cleaners, and car wash products, where workplace protections can be implemented to avoid unsafe exposures.
Sodium Dodecyl Sulfate is also used in lower concentrations in household and personal care products such as cleaning products, toothpastes, shampoos, and shaving foams.

Sodium Dodecyl Sulfate has been an ingredient in shampoos since the 1930s.
Sodium Dodecyl Sulfate works as a surfactant, trapping oil and dirt in hair so it can rinse away with water.

Personal Care Products
An effective foaming agent, Sodium Dodecyl Sulfate can help create a rich lather in products like body and hand wash, facial cleansers and bubble.
Likewise, Sodium Dodecyl Sulfate helps create the foaming action in toothpaste and also helps remove food particles from teeth.

Cleaning Products
Sodium Dodecyl Sulfate is an effective surfactant used in household cleaning products to help remove oily stains and residues, such as food stains in carpets.
Because of its ability to break down oil and grease, Sodium Dodecyl Sulfate also is an ingredient in many industrial cleaning products, such as engine degreasers and industrial strength detergents.

Food Additive
As a food additive, Sodium Dodecyl Sulfate is used as an emulsifier or thickener.
For example, Sodium Dodecyl Sulfate helps make marshmallows and dried egg products light and fluffy.
Sodium Dodecyl Sulfate also helps acids mix better with liquids, for example in fruit juices and punches.

Sodium Dodecyl Sulfate is frequently used as a surfactant, or foaming agent.
Sodium Dodecyl Sulfate may also serve as an emulsifier, helping oil based and water based ingredients to stay mixed.
In many of our toothpastes SLS is used as a surfactant and helps to properly disperse the ingredients during brushing, and ensures easy rinsing and removal of debris (i.e. food particles).

Sodium Dodecyl Sulfate may be derived from either petroleum based or vegetable based sources.
The oils can be split into glycerin and the component fatty acids, one of which is lauric acid.
The lauric acid is isolated and then hydrogenated to form the lauryl alcohol.

Alternately, the whole oil can be esterified and then hydrogenated to form the fatty alcohols of which lauryl alcohol would be isolated by fractionation.
The lauryl alcohol is then combined with sulfur which then forms the salt, Sodium Dodecyl Sulfate.

Sodium Dodecyl Sulfate is a cleansing agent known for being too good at the job and potentially irritating the skin.
But, on the positive side, it can produce copious, creamy and luxurious foam compared to the more gentle and thus nowadays much more commonly used Sodium Dodecyl Sulfate.

In fact, SLS is so good at irritating the skin that it is very commonly used in dermatological studies just for that. It is a so-called "primary irritant", a substance that irritates the skin in one go (without prior sensitization) but doesn't do any other big harm (such as being carcinogenic or systematically toxic - those claims are not true).
Also, the formula can greatly influence the irritating potential of SLS, and mixing it with other cleaning agents makes it milder.

If it's not in a cleanser, it works as an emulsifier or even as a penetration enhancer for active materials.

Synonyms:
151-21-3
SODIUM LAURYL SULFATE
Sodium dodecylsulfate
Sodium lauryl sulphate
Sodium dodecyl sulphate
Dodecyl sodium sulfate
Neutrazyme
Sodium n-dodecyl sulfate
Irium
Dodecyl sulfate sodium salt
Dodecyl sulfate, sodium salt
Sulfuric acid monododecyl ester sodium salt
Anticerumen
Duponal
Duponol
Gardinol
Dreft
Aquarex methyl
Duponol methyl
Solsol needles
Stepanol methyl
Duponol waqa
Stepanol wac
Stepanol waq
Duponol qx
Richonol af
Perlandrol L
Perlankrol L
Sipex sb
Sipex sd
Standapol wa-ac
Stepanol me dry
Duponol Me
Richonol A
Richonol C
Sintapon L
Duponol C
Maprofix LK
Standapol WAQ
Stepanol ME
Stepanol WA
Akyposal SDS
Carsonol SLS
Maprobix NEU
Maprofix NEU
Maprofix WAC
Aquarex ME
Dupanol WAQ
Duponol QC
Duponol WA
Duponol WA dry
Duponol WAQ
Empicol LPZ
Hexamol SLS
Melanol CL
Duponal WAQE
Duponol WAQE
Duponol WAQM
Lanette Wax-S
Sterling wa paste
Conco sulfate WA
Conco sulfate WN
Nikkol SLS
Orvus WA Paste
Sipex OP
Sipex SP
Sipex UB
Sipon LS
Sipon PD
Sipon WD
Detergent 66
Montopol La Paste
Sipon LSB
Maprofix WAC-LA
Sterling WAQ-CH
Cycloryl 21
Cycloryl 31
Stepanol WA Paste
Conco Sulfate WAG
Conco Sulfate WAN
Conco Sulfate WAS
Quolac EX-UB
Odoripon Al 95
Avirol 118 conc
Cycloryl 580
Cycloryl 585N
Lauryl sulfate sodium salt
Lauyl sodium sulfate
Maprofix 563
Sinnopon LS 95
Stepanol T 28
Steinapol NLS 90
Empicol LS 30
Empicol LX 28
Lauryl sodium sulfate
Melanol CL 30
NALS
Rewopol NLS 30
Standapol waq special
Standapol was 100
Sinnopon LS 100
Stepanol WA-100
Carsonol SLS Special
Standapol 112 conc
Stepanol ME Dry AW
Avirol 101
Emersal 6400
Monogen Y 100
Carsonol SLS Paste B
sodium;dodecyl sulfate
Stepanol methyl dry aw
Berol 452
Emal 10
EMAL O
Sipon LS 100
n-Dodecyl sulfate sodium
Sodium monolauryl sulfate
Monododecyl sodium sulfate
Sodiumlauryl ether sulfate
Conco sulfate WA-1200
Conco sulfate WA-1245
Dehydag sulfate GL emulsion
Product no. 75
Product no. 161
MFCD00036175
Emulsifier no. 104
CHEBI:8984
UNII-368GB5141J
P and G Emulsifier 104
Sodium lauryl sulfate ether
Sodium Laurylsulfate
Sulfuric acid monododecyl ester sodium salt (1:1)
SLS
Texapon K 1296
NCI-C50191
Laurylsulfuric Acid Sodium Salt
Natriumalkyl(C8-C20)-sulfate
Dodecyl alcohol, hydrogen sulfate, sodium salt
Dodecylsulfuric Acid Sodium Salt
Finasol osr2
Incronol SLS
Natriumlaurylsulfat
368GB5141J
NSC-402488
NCGC00091020-03
E487
Jordanol SL-300
Finasol osr(sub 2)
Dodecyl sulfate sodium
Monagen Y 100
Perklankrol ESD 60
Caswell No. 779
Natrium laurylsulfuricum
DSSTox_CID_6031
DSSTox_RID_77989
Sodium monododecyl sulfate
DSSTox_GSID_26031
12738-53-3
12765-21-8
1334-67-4
Laurylsiran sodny [Czech]
Lauryl sulfate, sodium salt
Dehydrag sulfate gl emulsion
Dehydag sulphate GL emulsion
Laurylsiran sodny
Rhodapon UB
Sodium lauryl sulfate 30%
sodiumdodecylsulfate
CAS-151-21-3
CCRIS 6272
Lauryl sulfate sodium
HSDB 1315
Sodium lauryl sulfate, dental grade
EINECS 205-788-1
EPA Pesticide Chemical Code 079011
NSC 402488
CP 75424
Empicol
AI3-00356
Sodium lauryl sulfate [JAN:NF]
sodiumlauryl sulfate
Sodium laurilsulfate
sodium dodecylsulphate
Sodium dedecyl sulfate
Sodium-dodecyl-S-SDS
IPC-SDS
sodium n-dodecyl sulphate
Sodium Lauryl Sulfate NF
lauryl sulphate sodium salt
EC 205-788-1
dodecyl sulphate sodium salt
SCHEMBL1102
C12H25NaO4S
sodium dodecyl sulfate (sds)
CHEMBL23393
Sodium dodecyl sulfate, 99%
sodium dodecyl sulphate (sds)
sodium 2-dodecoxyethyl sulfate
Sodium dodecyl sulphate solution
DTXSID1026031
dodecyl sulfuric acid sodium salt
Dodecyl sulphuric acid sodium salt
Sodium lauryl sulfate (JP17/NF)
BCP30594
CS-B1770
Tox21_111059
Tox21_201614
Tox21_300149
BDBM50530482
AKOS015897278
AKOS025147308
Tox21_111059_1
DB00815
Dodecyl sulfuric acid ester sodium salt
NCGC00091020-01
NCGC00091020-02
NCGC00254225-01
NCGC00259163-01
NCGC00274082-01
AS-14730
M361
Lauryl Sulfate, Sodium Salt (25% Aq.)
D1403
FT-0603358
FT-0700721
I0352
S0588
D01045
F16341
S-4600
S-4601
Sodium dodecyl sulfate, 10% solution in water
SODIUM DODECYL SULFATE BIOTECH GRD 100G
Q422241
Sodium n-dodecyl sulfate, 98%, for electrophoresis
Sodium n-dodecyl sulfate (SDS), 20% aqueous solution
F0001-0539
Z169572898
SODIUM DODECYLBENZENESULFONATE ( Dodécylbenzènesulfonate de sodium )
SODIUM DODOXYNOL-40 SULFATE Nom INCI : SODIUM DODOXYNOL-40 SULFATE Classification : Sulfate, Composé éthoxylé Ses fonctions (INCI) Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM DODOXYNOL-40 SULFATE
cas no 6381-77-7 Isoascorbic acid, sodium salt; D-Araboascorbic acid, monosodium salt; D-erythro-Hex-2-enonic acid, gamma-lactone, monosodium salt; Erythorbic Acid Monosodium Salt; Monosodium erythorbate; Neo-cebitate; 2,3-Didehydro-3-O-sodio- D-erythro- hexono-1,4-Lactone; 2,3-Didehidro-3-O-sodio-D- eritro-hexono- 1,4-Lactona: 2,3-Didéhydro-3-O-sodio-D- érythro-hexono-1,4-Lactone; Sodium D-araboascorbate; sodium D-isoascorbate;
SODIUM ERYTHORBATE
SYNONYMS Isoascorbic acid, sodium salt; D-Araboascorbic acid, monosodium salt; D-erythro-Hex-2-enonic acid, gamma-lactone, monosodium salt; Erythorbic Acid Monosodium Salt; Monosodium erythorbate; Neo-cebitate; 2,3-Didehydro-3-O-sodio- D-erythro- hexono-1,4-Lactone; 2,3-Didehidro-3-O-sodio-D- eritro-hexono- 1,4-Lactona: 2,3-Didéhydro-3-O-sodio-D- érythro-hexono-1,4-Lactone; Sodium D-araboascorbate; sodium D-isoascorbate; CAS NO. 6381-77-7
SODIUM ERYTHORBATE ( Érythorbate de sodium ) Sodium isoascorbate
ETHYL 4-HYDROXYBENZOATE SODIUM SALT ETHYL-4-HYDROXYBENZOIC ACID SODIUM SALT ETHYL-P-HYDROXYBENZOATE SODIUM SALT p-Hydroxybenzoic acid ethyl ester sodium salt sodium 4-ethoxycarbonylphenoxide SODIUM ETHYL 4-HYDROXYBENZOATE SODIUM ETHYL-P-HYDROXYBENZOATE benzoicacid,4-hydroxy-,ethylester,sodiumsalt Benzoicacid,p-hydroxy-,ethylester,sodiumderiv. 4-Hydroxybenzoic acid ethyl ester sodium salt SODIUM ETHYLPARABEN EthylParabenSodium ETHYL4-HYDROBENZOATESODIUMSALT BENZOICACID,PARA-HYDROXY-,ETHYLESTER,SODIUMSALT 4-(Sodiooxy)benzoic acid ethyl ester 4-Sodiooxybenzoic acid ethyl ester CAS :35285-68-8
SODIUM ETHYL PARABENE
Chemical name Sodium Ethyl p-Hydroxybenzoate 35285-68-8Sodium Ethylparaben Sodium Ethyl paraben is a broad spectrum antimicrobial agent designed for preservation of a wide range of cosmetics, toiletries pharmaceuticals. Nipagin A Sodium is suitable to preserve both rinse- off and leave- on formulations. Nipagin A Sodium is effective against bacteria, molds and yeast. EC / List no.: 252-487-6 CAS no.: 35285-68-8 Mol. formula: C9H9NaO3 Sodium Ethyl P-hydroxybenzoate Odor: characteristic Use: Sodium ethyl p-hydroxybenzoate is widely used in food and pharmaceutical and textile industry for its antiseptic property. Sodium Ethylparaben is also can be used in industries such as cosmetics, feed and so on. Synonyms: benzoic acid, 4-hydroxy-, ethyl ester, sodium salt benzoic acid, p-hydroxy-, ethyl ester, sodium deriv. ethyl p-hydroxybenzoate, sodium salt ethylparaben sodium ethylparaben, sodium salt 4- hydroxybenzoic acid, ethyl ester, sodium salt sodium 4-ethoxycarbonyl phenoxide sodium 4-ethoxycarbonylphenoxide sodium ethyl 4-hydroxybenzoate sodium ethyl p-hydroxybenzoate sodium ethyl paraben sodium;4-ethoxycarbonylphenolate Synonym: Ethyl 4-hydroxybenzoate sodium salt, p-Hydroxybenzoic acid ethyl ester sodium salt, Ethylparaben sodium salt Sodium Ethyl paraben is a Sodium salt of ethylparaben Sodium Ethylparaben uses and applications include: Antimicrobial, preservative, bactericide, fungicide for foods, beer, pharmaceuticals; preservative in cosmetics Sodium Ethylparaben is a water-soluble antiseptic mainly used as a safe, high efficiency, broad-spectrum antibiotic for cosmetics. Sodium Ethyl paraben is in the paraben family of preservatives used by the food, pharmaceutical, and personal care product industries. INCI designation Sodium Ethylparaben. Product properties *) Appearance: White powder Chemical and physical data pH 9.5- 10.5 Water content: max. 5.0 % Assay by non aqueous titration: 99 - 102 % Uses: Sodium Ethyl paraben is a broad spectrum antimicrobial agent designed for preservation of a wide range of cosmetics, toiletries pharmaceuticals. Sodium Ethyl paraben is suitable to preserve both rinse- off and leave- on formulations. Sodium Ethylparaben is effective against bacteria, molds and yeast. The recommended use level of Nipagin A Sodium to preserve most product types is normally in the range of 0.1- 0.3 % based on the total weight of the finished product. The Paraben esters have many advantages as preservatives,like broad spectrum antimicrobial activity, effective at low use concentrations, compatible with a wide range of cosmetic ingredients, colourless, odourless, well documented toxicological and dermatological acceptability based on human experience (used in cosmetics, food and pharmaceuticals since 1930ies), p-Hydroxybenzoic Acid and a number of its esters occur naturally in a variety of plants and animals, stable and effective over a wide pH- range, etc. The Sodium Parabens, like Sodium Ethylparaben have several additional advantages: - Nipagin A Sodium is highly soluble in cold water for ease of addition. - No heating stage required for incorporation, thus saving energy and plant occupancy. - Increased antimicrobial activity at alkaline pH. Applications: Sodium Ethylparaben is designed for preservation of a wide range of cosmetics and toiletries. Sodium Ethylparaben is suitable to preserve both rinse- off and leave- on formulations. Formulations which are prone to bacteria contamination an additional antibacterial preservative, like Nipaguard DMDMH might be necessary to add as Sodium Ethylparaben provides a higher efficacy against fungi than against bacteria. Solubility Water up to 50 % Sodium Ethylparaben SINGLE PRESERVATIVE Sodium Ethylparaben is a highly water-soluble short-chain paraben in sodium salt form. The major benefit offered by the sodium salts is their high solubility in cold water, thereby enabling the introduction of parabens without heating or pre-dissolving in solvents. Benefits Sodium Ethylparaben has high solubility in cold water Sodium Ethylparaben performs broad spectrum of activity against bacteria and fungi Sodium Ethylparaben shows effectiveness at low concentrations Sodium Ethylparaben has stability over a broad pH-range Water-soluble Biodegradability at environmental concentrations Global acceptance in personal care applications Ethylparaben Sodium, also known as Ethyl paraben or Ethyl parahydroxybenzoate, can be used as a food additive and as an antifungal preservative Incorporation: Sodium Ethylparaben is highly soluble in water and so easily incorporated into cosmetic formulations. It is important to note that, whilst the aqueous solubility in alkaline solution is high, if the pH of the formulated product is acidic the sodium salt reverts to the ester and the low solubility is regained. Microbial activity: Sodium Ethylparaben has a broad spectrum of activity which includes the following common spoilage organisms. Microorganisms MIC level (%) Gram-negative bacteria Pseudomonas aeruginosa 0.113 Escherichia coli 0.056 Klebsiella pneumoniae 0.056 Serratia marcescens 0.056 Proteus vulgaris 0.068 Salmonella enteritidis 0.046 Gram-positive bacteria Staphylococcus aureus 0.079 Streptococcus haemolyticus 0.068 Bacillus cereus 0.028 Yeasts Candida albicans 0.079 Saccharomyces cerevisiae 0.056 Molds Aspergillus niger 0.045 Technical Data Appearance :Powder Active Substance (ca.): 100% INCI-Name: Sodium Ethylparaben Applications Aqueous concentrates may be prepared up to 40% in strength. The concentrate may then be added to the process, preferably slowly and with rapid mixing. Due to the high pH of aqueous solutions of sodium parabens, the pH of the final product requires adjustment. The aqueous solution should be used within a short time of preparation as prolonged storage will result in alkaline hydrolysis of the esters. It is important to note that, at the target pH of the formulation, the parabens will exist as the free esters and not as salts and, therefore, the solubility will also be that of the free esters. Use of the sodium salts will facilitate introduction of the parabens; it will not allow higher concentrations to be used compared with the free esters. pH stability: Sodium Ethylparaben remains fully stable over a wide pH range from 3.0- 11.0. Aqueous solutions of Nipagin A Sodium are not long- term stable at alkaline pH. Temperature stability The recommended maximum handling temperature is 80°C. Storage instructions Sodium Ethylparaben is stable in sealed original containers. Further information on handling, storage and dispatch is given in the EC safety data sheet. Sodium Ethylparaben is a broad spectrum antimicrobial agent designed for preservation of a wide range of cosmetics, toiletries pharmaceuticals. It is suitable to preserve both rinse- off and leave- on formulations. This product is highly soluble in cold water, which adds to its ease of addition to formulations. Sodium Ethylparaben. Sodium Ethyl paraben provides a broad spectrum of activity against bacteria & fungi. Sodium Ethyl paraben is a short-chain paraben in sodium salt form. Sodium Ethylparaben offers high solubility in cold water, low order of toxicity and stability over a broad pH-range. Sodium Ethylparaben exhibits effectiveness at low concentrations. Sodium Ethylparaben shows good biodegradability at environmental concentrations. Sodium Ethylparaben is used in all kinds of personal care products. Parabene Product description Parabens - esters of the para-hydroxybenzoic acid, are used as preservatives for pharmaceuticals, cosmetics as well as food applications due to their effective antibacterial and fungicidal properties. The grades comply to different pharmaceutical standards as EP, BP or USP. More products available upon request. INCI CAS Methyl Paraben 99-76-3 Sodium Methyl Paraben 5026-62-0 Propyl Paraben 94-13-3 Sodium Propyl Paraben 35285-69-9 Ethyl Paraben 120-47-8 Sodium Ethyl Paraben 35285-68-8 Butyl Paraben 94-26-8 Preservative for the cosmetic industry. Sodium Ethyl p-Hydroxybenzoate, designed for preservation of a wide range of cosmetics and toiletries. Sodium Ethyl Paraben is suitable to preserve both rinse- off and leave- on formulations. Formulations which are prone to bacteria contamination an additional antibacterial preservative might be necessary to add as it provides a higher efficacy against fungi than against bacteria. Sodium Ethyl Paraben is broad spectrum antimicrobial agent designed for preservation of a wide range of cosmetics, toiletries pharmaceuticals. Sodium Ethyl Paraben is suitable to preserve both rinse- off and leave- on formulations. Sodium Ethyl Paraben is effective against bacteria, molds and yeast. Sodium Ethyl Paraben's usage level to preserve most product types is normally in the range of 0.1- 0.3 % based on the total weight of the finished product. Sodium Ethyl Paraben is soluble in cold water for ease; No heating stage required for incorporation, thus saving energy and plant occupancy; Increased antimicrobial activity at alkaline pH.pH stability; remains fully stable over a wide pH range from 3.0- 11.0. Aqueous solutions are not long- term stable at alkaline pH.max. temperature 80°C. This substance is one of the parabens family. Parabens are esters formed by p-hydroxybenzoic acid and an alcohol. They are largely used as biocides in cosmetics and toiletries, medicaments, or food. They have synergistic power with biocides. Parabens can induce allergic contact dermatitis, mainly in chronic dermatitis and wounded skin. • p-Hydroxybenzoic acid ethyl ester sodium salt • SODIUM ETHYL-P-HYDROXYBENZOATE • SODIUM ETHYL 4-HYDROXYBENZOATE • sodium 4-ethoxycarbonylphenoxide • benzoicacid,4-hydroxy-,ethylester,sodiumsalt • Benzoicacid,p-hydroxy-,ethylester,sodiumderiv. • ETHYL-P-HYDROXYBENZOATE SODIUM SALT • ETHYL-4-HYDROXYBENZOIC ACID SODIUM SALT • ETHYL 4-HYDROXYBENZOATE SODIUM SALT • 4-Hydroxybenzoic acid ethyl ester sodium salt • SODIUM ETHYLPARABEN • EthylParabenSodium • ETHYL4-HYDROBENZOATESODIUMSALT • BENZOICACID,PARA-HYDROXY-,ETHYLESTER,SODIUMSALT • 4-(Sodiooxy)benzoic acid ethyl ester • 4-Sodiooxybenzoic acid ethyl ester • p-Hydroxybenzoic acid ethyl ester sodium salt,sodium salt • Sodium 4-(ethoxycarbonyl)phenolate • Benzoic acid,4-hydroxy-, ethyl ester, sodiuM salt (1:1) • Sodium Ethyl-p-hydroxyl Benzoate • 35285-68-8 • Sodium 4-(ethoxycarbonyl) • p-Hydroxybenzoic acid ethyl ester sodium salt fandachem • odium 4-(ethoxycarbonyl)phenolate • 35285-68-8 • C9H9O3Na • Benzoic acid Series • Aromatic Esters Ethyl Paraben Sodium - Names and Identifiers Name p-Hydroxybenzoic acid ethyl ester sodium salt,sodium salt Synonyms p-Hydroxybenzoic acid ethyl ester sodium salt SODIUM ETHYL-P-HYDROXYBENZOATE SODIUM ETHYL 4-HYDROXYBENZOATE sodium 4-ethoxycarbonylphenoxide benzoicacid,4-hydroxy-,ethylester,sodiumsalt Benzoicacid,p-hydroxy-,ethylester,sodiumderiv. ETHYL-P-HYDROXYBENZOATE SODIUM SALT ETHYL-4-HYDROXYBENZOIC ACID SODIUM SALT sodium salt Ethyl 4-hydroxybenzoate,sodium salt Sodium Ethylparaben Ethyl Paraben Sodium sodium 4-(ethoxycarbonyl)phenolate benzoic acid, 4-hydroxy-, ethyl ester, sodium salt (1:1) Ethyl p-hydroxybenzoate sodium Parabens are a family of related ingredients commonly used as preservatives in cosmetics and personal care products. They help prevent the growth of harmful bacteria and mold, protecting both products and consumers. Parabens are highly effective and widely used preservatives that enhance the shelf life and safety of products including all types of cosmetics, as well as foods and drugs, and protect the families who trust and enjoy them. The most commonly used parabens in cosmetics are methylparaben, ethylparaben, propylparaben, and butylparaben. Paraben preservatives all share para-hydroxybenzoic acid, or PHBA, as a common chemical structure. PHBA occurs naturally in many fruits and vegetables. The parabens used in cosmetics are identical to those found in nature, and are quickly eliminated by the body. Any product that contains water is susceptible to being spoiled by the growth of fungi or bacteria, which could cause problems such as discoloration, malodor, or breakdown of the product. Under certain conditions, an inadequately preserved product can become contaminated, allowing harmful levels of microorganisms to grow. Parabens are highly effective preservatives that protect products against such changes, thus enhancing the shelf life and safety of products, and have been used safely for decades. Ethylparaben, also known as e-214 or aseptin a, belongs to the class of organic compounds known as p-hydroxybenzoic acid alkyl esters. These are aromatic compounds containing a benzoic acid, which is esterified with an alkyl group and para-substituted with a hydroxyl group. It is used as an antifungal preservative. Sodium ethyl para-hydroxybenzoate, the sodium salt of ethylparaben, has the same uses and is given the E number E215. Ethylparaben is an extremely weak basic (essentially neutral) compound (based on its pKa). Its formula is HO-C6H4-CO-O-CH2CH3. Ethylparaben is a mild and phenolic tasting compound. Outside of the human body, ethylparaben has been detected, but not quantified in, alcoholic beverages. This could make ethylparaben a potential biomarker for the consumption of these foods. Ethylparaben (ethyl para-hydroxybenzoate) is the ethyl ester of p-hydroxybenzoic acid. Ethylparaben is a potentially toxic compound. As a food additive, it has E number E214. This information is based on our present state of knowledge and is intended to provide general notes on our products and their uses. It should not therefore be construed as guaranteeing specific properties of the products described on their suitability for a particular application. Any existing industrial property rights must be observed. The quality of our products is guaranteed under our General Conditions of Sale.
SODIUM ETHYL P-HYDROXYBENZOATE (SODIUM ETHYL PARABEN)
Sodium 2-ethylhexyl sulfate; 2-Ethylhexylsulfate, sodium salt; ALKOHOLSULFAT, NA-SALZ I-C8; Sodium (2-ethylhexyl) alcohol sulfate; sodium (2-ethylhexyl) sulfate; Sodium 2-ethylhexyl sulfate; SODIUM ETHYLHEXYL SULFATE, N° CAS : 126-92-1, Nom INCI : SODIUM ETHYLHEXYL SULFATE. Nom chimique : Sodium etasulfate. N° EINECS/ELINCS : 204-812-8. Classification : Sulfate Ses fonctions (INCI). Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile). 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 : Ethalsulfate de sodium; ETHALSULFATE SODIQUE; ETHASULFATE SODIUM; ETHYL-2 HEXYLSULFATE DE SODIUM. Noms anglais : 2-ETHYL-1-HEXANOL SODIUM SULFATE ; 2-ETHYLHEXYL SODIUM SULFATE; SODIUM 2-ETHYLHEXYL SULFATE; SODIUM ETASULFATE; SODIUM ETHASULFATE; SULFURIC ACID, MONO(2-ETHYLHEXYL) ESTER, SODIUM SALT; Sodium etasulfate. CAS names: Sulfuric acid, mono(2-ethylhexyl) ester, sodium salt (1:1). : 2-ethylhexyl hydrogen sulfate; 2-ethylhexyl hydrogen sulfate; sodium; 2-Ethylhexylsulfate, sodium salt; ALKOHOLSULFAT, NA-SALZ I-C8; Sodium (2-ethylhexyl) alcohol sulfate; sodium (2-ethylhexyl) sulfate; Sodium 2-ethylhexyl sulfate; sodium etasulphate; sodium ethasulfate; Sodium-2-ethylhexyl sulphate; Sodium-2-ethylhexylsulphate; sodium;2-ethylhexyl sulfate; Sulfuric acid,mono(2-ethylhexyl)ester,sodium salt; 126-92-1 [RN]; 12838560LI 1487; 204-812-8 [EINECS]; 2-Ethylhexyl sulfate sodium salt; 5177087; étasulfate de sodium ; etasulfato de sodio [Spanish] ; MFCD00042047 [MDL number]; MP0700000; natrii etasulfas [Latin] ; Natrium-2-ethylhexylsulfat [German] ; Sodium 2-ethylhexyl sulfate; sodium etasulfate; sodium ethasulfate; Sulfate de sodium et de 2-éthylhexyle [French] ; sulfuric acid, 2-ethylhexyl ester, sodium salt; Sulfuric acid, 2-ethylhexyl ester, sodium salt (1:1); tergemist; UNII:12838560LI; натрия этасульфат [Russian] ; إيتاسولفات صوديوم [Arabic]; 依他硫酸钠 [Chinese]; 11099-08-4 secondary RN [RN] ; 1-Hexanol, 2-ethyl-, hydrogen sulfate, sodium salt; 1-Hexanol, 2-ethyl-, sulfate, sodium salt; 2-Ethyl-1-hexanol hydrogen sulfate sodium salt; 2-Ethyl-1-hexanol sodium sulfate; 2-ethyl-1-hexanol sulfate sodium salt; 2-ethylhexyl hydroxysulfonate, sodium salt; 2-Ethylhexyl sodium sulfate; 2-Ethylhexylsiran sodny [Czech]; 2-Ethylhexylsulfate sodium; 2-Ethylhexylsulphate,sodium salt 75037-31-9 secondary RN [RN]; ammonium 2-ethylhexyl sulphate; Avirol SA 4106; Carsonol SHS; emcol d 5-10; emersal 6465; Etasulfate de sodium [French]; Etasulfato sodico [Spanish] ; Ethasulfate sodium; Hexanol, 2-ethyl-, hydrogen sulfate, sodium salt; Lugalvan TC-EHS; Lutensit TC-EHS; Mono(2-ethylhexyl) sulfate sodium salt; mono(2-ethylhexyl)sulfate sodium salt ; Newcol 1000SN; nia proof 08; Niaproof ; Niaproof 08; Nissan Sintrex EHR; pentrone on; propaste 6708; Rewopol NEHS 40; Rhodapon BOS; Sinolin SO 35; Sintrex EHR; sipex bos ;Sodium (2-Ethylhexyl)Alcohol Sulfate; sodium 2-ethylhexyl sulphate; Sodium Ethylhexyl Sulfate; Sodium mono(2-ethylhexyl) sulfate; Sodium octyl sulfate, iso-; Sodium(2-ethylhexyl)alcohol sulfate ; sodium; sulfuric acid 2-ethylhexyl ester; sodium-2-ethylhexyl sulfate; sodium2-ethylhexylsulfate; sodiumisooctylsulfate; Sole Tege TS 25; Sulfuric Acid Mono(2-ethylhexyl) Ester Sodium Salt ; Sulfuric acid, mono(2-ethylhexyl) ester, sodium salt; Supralate SP; Tergimist; tergitol 08; Tergitol anionic 08; Tergitol-8; Tergitol-8|Niaproof-8|Sodium 2-ethylhexyl sulfate; Texapon 842; Texapon 890; Witcolate D 5-10. Sodium 2-ethylhexyl sulfate is a low-foaming anionic surfactant with excellent wetting properties and outstanding stability in highly electrolyte, alkaline and acidic systems. It is a profound hydrotropic and wetting agent suitable for use in the production of liquid detergents for household and industrial use such as hard-surface cleaners and alkaline and acid metal degreasers. Owing to its wetting and penetrating properties Sodium 2-ethylhexyl sulfate is used as a mercerizing agent in textile industry, in metal galvanization, pickling and brightening, in lye washing and peeling solutions for fruits and vegetables, in fountain solutions for offset printing, wallpaper removal solutions etc. Sodium 2-ethylhexyl sulfate uses and applications include: Wetting agent for electroplating baths, alkaline textile processing aids, industrial cleaners; coemulsifier for polymerization; viscous control in adhesives; food packaging adhesives; in paperpaperboard in contact with aqueousfatty foods; surfactant, detergent, wetting agent, emulsifier, penetrant, stabilizer for cosmetics, pharmaceuticals, textiles, household and industrial cleaners, metal cleaning, paints, plastics, rubber, food packaging and processing, adhesives; washinglye peeling of fruits and vegetables. product carries excellent wetting, spreading and hydrotropic proterties. This material can tolorate alkanline condition. Sodium Ethylhexyl Sulfate is mainly applied as wetting agent in alkaline solutions such as in the textile industry. Sodium Ethylhexyl Sulfate can also be added to the aerosol fulmulated product as the spreading agent. Also the material can be used as the hydrotropic agent.
SODIUM ETHYLHEXYL SULFATE ( ETHYL-2 HEXYLSULFATE DE SODIUM) Sulfate de sodium et de 2-éthylhexyle
cas no 120-47-87 Ethyl 4-hydroxybenzoate; Sodium ethylp-hydroxybenzoate; Sodium ethyl p-hydroxybenzoate;
SODIUM ETHYLPARABEN
Ethyl p-hydroxybenzoate; SODIUM ETHYLPARABEN, N° CAS : 35285-68-8. Nom INCI : SODIUM ETHYLPARABEN. Nom chimique : Sodium 4-ethoxycarbonylphenoxide; N° EINECS/ELINCS : 252-487-6; Classification : Paraben, Perturbateur endocrinien suspecté, Règlementé, Conservateur. Ses fonctions (INCI) : Conservateur : Inhibe le développement des micro-organismes dans les produits cosmétiques.4-Hydroxybenzoic acid, ethyl ester, sodium salt; Benzoic acid, 4-hydroxy-, ethyl ester, sodium salt; Benzoic acid, p-hydroxy-, ethyl ester, sodium deriv.; Ethyl p-hydroxybenzoate, sodium salt ; Ethylparaben sodium; Ethylparaben, sodium salt; Sodium 4-ethoxycarbonylphenoxide; Sodium ethylparaben. CAS names : Benzoic acid, 4-hydroxy-, ethyl ester, sodium salt (1:1); : Ethyl-4-hydroxybenzoat, Natriumsalz; Ethyl-4-hydroxybenzoat, sodium salt; p-Hydroxybenzoic acid ethyl ester sodium salt; sodium 4-(ethoxycarbonyl)benzen-1-olate; sodium 4-(ethoxycarbonyl)phenolate; sodium;4-ethoxycarbonylphenolate; Sodium ethyl p-hydroxybenzoate; 252-487-6 [EINECS]; 35285-68-8 [RN]; 4-(Éthoxycarbonyl)phénolate de sodium [French] ; Benzoic acid, 4-hydroxy-, ethyl ester, sodium salt (1:1) ; E215; ETHYLPARABEN SODIUM; Natrium-4-(ethoxycarbonyl)phenolat [German] [ACD/IUPAC Name]; p-hydroxybenzoic acid ethyl ester sodium salt; Sodium 4-(ethoxycarbonyl)phenolate [ACD/IUPAC Name]; Sodium ethylparaben Z0D00IVA10 [35285-68-8] 4-ethoxycarbonylphenolate 4-Hydroxybenzoic acid, ethyl ester, sodium salt 5026-62-0 [RN] Benzoic acid, 4-hydroxy-, ethyl ester, sodium salt Benzoic acid, 4-hydroxy-, methyl ester, sodium salt BENZOIC ACID, p-HYDROXY-, ETHYL ESTER, SODIUM DERIV. BENZOIC ACID, p-HYDROXY-, METHYL ESTER, SODIUM DERIV. Bonomold OMNa EINECS 225-714-1 EINECS 252-487-6 Ethyl p-hydroxybenzoate, sodium salt ETHYL4-HYDROXYBENZOATESODIUMSALT Ethylparaben sodium salt Ethylparaben, sodium salt Methyl 4-hydroxybenzoate sodium salt METHYL P-HYDROXYBENZOATE, SODIUM SALT Methylparaben sodium [NF] Methylparaben sodium (NF) Methylparaben sodium [USAN] [USAN] methylparaben, sodium salt MFCD00016475 [MDL number] NIPASEPT SODIUM Preserval MS Sodium [ACD/Index Name] [ACD/IUPAC Name] [Wiki] sodium 4-(ethoxycarbonyl)benzen-1-olate SODIUM 4-(ETHOXYCARBONYL)BENZENOLATE Sodium 4-(methoxycarbonyl)phenolate [ACD/IUPAC Name] sodium 4-carbethoxyphenolate sodium 4-carbomethoxyphenolate sodium 4-ethoxycarbonylphenolate Sodium 4-ethoxycarbonylphenoxide sodium 4-methoxycarbonylphenolate sodium and 4-ethoxycarbonylphenolate SODIUM ETHYL PARABEN Sodium Ethyl Parahydroxybenzoate Sodium ethyl p-hydroxybenzoate, tech. Sodium methyl 4-hydroxybenzoate Sodium methyl p-hydroxybenzoate Sodium methylparaben Sodium p-methoxycarbonylphenoxide Sodium, (p-carboxyphenoxy)-, methyl ester (7CI) sodium;4-ethoxycarbonylphenolate Solparol ST5405340 UNII:Z0D00IVA10 UNII-F57SQP06GK UNII-Z0D00IVA10
SODIUM FORMATE
Sodium Formate Sodium formate, HCOONa, is the sodium salt of formic acid, HCOOH. It usually appears as a white deliquescent powder. Properties Chemical formula HCOONa Molar mass 68.007 g/mol Appearance white granules deliquescent Density 1.92 g/cm3 (20 °C) Melting point 253 °C (487 °F; 526 K) Boiling point decomposes Solubility in water 43.82 g/100 mL (0 °C) 97.2 g/100 mL (20 °C) 160 g/100 mL (100 °C) Solubility insoluble in ether soluble in glycerol, alcohol, formic acid Preparation For commercial use, sodium formate is produced by absorbing carbon monoxide under pressure in solid sodium hydroxide at 130 °C and 6-8 bar pressure: CO + NaOH → HCO2Na Because of the low-cost and large-scale availability of formic acid by carbonylation of methanol and hydrolysis of the resulting methyl formate, sodium formate is usually prepared by neutralizing formic acid with sodium hydroxide. Sodium formate is also unavoidably formed as a by-product in the final step of the pentaerythritol synthesis and in the crossed Cannizzaro reaction of formaldehyde with the aldol reaction product trimethylol acetaldehyde [3-hydroxy-2,2-bis(hydroxymethyl)propanal]. In the laboratory, sodium formate can be prepared by neutralizing formic acid with sodium carbonate. It can also be obtained by reacting chloroform with an alcoholic solution of sodium hydroxide. CHCl3 + 4 NaOH → HCOONa + 3 NaCl + 2 H2O or by reacting sodium hydroxide with chloral hydrate. C2HCl3(OH)2 + NaOH → CHCl3 + HCOONa + H2O The latter method is, in general, preferred to the former because the low aqueous solubility of CHCl3 makes it easier to separate out from the sodium formate solution, by fractional crystallization, than the soluble NaCl would be. Sodium formate may also be created via the haloform reaction between ethanol and sodium hypochlorite in the presence of a base. This procedure is well documented for the preparation of chloroform. Properties Physical properties Sodium formate crystallizes in a monoclinic crystal system with the lattice parameters a = 6,19 Å, b = 6,72 Å, c = 6,49 Å and β = 121,7°.[3] Chemical properties On heating, sodium formate decomposes to form sodium oxalate and hydrogen.[4] The resulting sodium oxalate can be converted by further heating to sodium carbonate upon release of carbon monoxide: As a salt of a weak acid (formic acid) and a strong base (sodium hydroxide) sodium formate reacts in aqueous solutions basic: A solution of formic acid and sodium formate can thus be used as a buffer solution. Sodium formate is slightly water-hazardous and inhibits some species of bacteria but is degraded by others. Uses Sodium formate is used in several fabric dyeing and printing processes. It is also used as a buffering agent for strong mineral acids to increase their pH, as a food additive (E237), and as a de-icing agent. In structural biology, sodium formate can be used as a cryoprotectant for X-ray diffraction experiments on protein crystals,[6] which are typically conducted at a temperature of 100 K to reduce the effects of radiation damage. Sodium formate plays a role in the synthesis of formic acid, it is converted by sulfuric acid via the following reaction equation: Sodium formate is converted with sulfuric acid to formic acid and sodium sulfate. The urticating hair of stinging nettles contain sodium formate as well as formic acid. Solid sodium formate is used as a non-corrosive agent at airports for de-icing of runways in mix with corrosion inhibitors and other additives, which rapidly penetrate solid snow and ice layers, detach them from the asphalt or concrete and melt the ice rapidly. Sodium formate was also used as a road deicer in the city of Ottawa from 1987 to 1988. The high freezing point depression e.g. in comparison to the still frequently used urea (which is effective but problematic due to eutrophication) effectively prevents the re-icing, even at temperatures below −15 °C. The thawing effect of the solid sodium formate can even be increased by moistening with aqueous potassium formate or potassium acetate solutions. The degradability of sodium formate is particularly advantageous with a chemical oxygen demand (COD) of 211 mg O2/g compared with the de-icing agents sodium acetate (740 mg O2/g) and urea with (> 2,000 mg O2/g).[8] Saturated sodium formate solutions (as well as mixtures of other alkali metal formates such as potassium and cesium formate) are used as important drilling and stabilizing aids in gas and oil exploration because of their relatively high density. By mixing the corresponding saturated alkali metal formate solutions any densities between 1,0 and 2,3 g/cm3 can be set. The saturated solutions are biocidal and long-term stable against microbial degradation. Diluted, on the other hand, they are fast and completely biodegradable. As alkali metal formates as drilling aids make it unnecessary to add solid fillers to increase the density (such as barytes) and the formate solutions can be recovered and recycled at the drilling site, formates represent an important advance in exploration technology. Applications Biotechnological Sodium formate is used as the carbon source for culturing bacteria. Sodium formate is also useful for increasing yields of DNA isolation by ethanol precipitation. Industrial Sodium formate is used in the textile industry to neutralize sulfuric acid waste streams and also as a photoresist while using aniline dyes. It is also a pickling agent in chrome tanning and helps to impede vulcanization of chloroprene in synthetic rubber production. In processing cotton for disposable cotton pads, Sodium formate is used to eliminate the buildup of static electricity. Concrete longevity Sodium formate is used to mitigate water damage to concrete by acting as a concrete sealant, while also being environmentally benign and cheaper than the commonly used epoxy alternative for sealing concrete against water permeation.[9] Food Sodium formate may be added to food as a seasoning, sometimes in the form of sodium diacetate, a one-to-one complex of Sodium formate and acetic acid,[10] given the E-number E262. It is often used to give potato chips a salt and vinegar flavor.[citation needed] Sodium formate (anhydrous) is widely used as a shelf-life extending agent, pH control agent[11] It is safe to eat at low concentration.[12] Buffer solution A solution of Sodium formate (a basic salt of acetic acid) and acetic acid can act as a buffer to keep a relatively constant pH level. This is useful especially in biochemical applications where reactions are pH-dependent in a mildly acidic range (pH 4–6). Heating pad A hand warmer containing a supersaturated solution of Sodium formate which releases heat upon crystallization Sodium formate is also used in heating pads, hand warmers, and hot ice. Sodium formate trihydrate crystals melt at 136.4 °F/58 °C[13] (to 137.12 °F/58.4 °C),[14] dissolving in their water of crystallization. When they are heated past the melting point and subsequently allowed to cool, the aqueous solution becomes supersaturated. This solution is capable of cooling to room temperature without forming crystals. By pressing on a metal disc within the heating pad, a nucleation center is formed, causing the solution to crystallize back into solid Sodium formate trihydrate. The bond-forming process of crystallization is exothermic.[15] The latent heat of fusion is about 264–289 kJ/kg.[13] Unlike some types of heat packs, such as those dependent upon irreversible chemical reactions, a Sodium formate heat pack can be easily reused by immersing the pack in boiling water for a few minutes, until the crystals are completely dissolved, and allowing the pack to slowly cool to room temperature. Preparation A crystal of Sodium formate trihydrate (length 1.7 centimetres) For laboratory use, Sodium formate is inexpensive and usually purchased instead of being synthesized. It is sometimes produced in a laboratory experiment by the reaction of acetic acid, commonly in the 5–8% solution known as vinegar, with sodium carbonate ("washing soda"), sodium bicarbonate ("baking soda"), or sodium hydroxide ("lye", or "caustic soda"). Any of these reactions produce Sodium formate and water. When a sodium and carbonate ion-containing compound is used as the reactant, the carbonate anion from sodium bicarbonate or carbonate, reacts with hydrogen from the carboxyl group (-COOH) in acetic acid, forming carbonic acid. Carbonic acid readily decomposes under normal conditions into gaseous carbon dioxide and water. This is the reaction taking place in the well-known "volcano" that occurs when the household products, baking soda and vinegar, are combined. Sodium formate appears in sodium methylate at 0.3% The slow decomposition in storage of 98-100% Sodium formate with liberation of carbon monoxide led to rupture of the sealed glass containers. In absence of gas leakage, a full 2.5 L bottle would develop a pressure of over 7 bar during 1 yr at 25 °C. Explosive decomposition of Sodium formate on a clean nickel ... surface was studied, using deuteroSodium formate. A full 1 L bottle of 96% Sodium formate burst when the ambient temp fell to -6 °C overnight and the contents froze and expanded. Gas pressure from previous partial decomposition may also have contributed. Sodium formate decomposes slowly during storage and more rapidly under fire conditions, forming carbon monoxide. Sodium formate is a reagent comprised of the organic chemical Sodium formate that cleaves proteins into peptides at the C- or N-terminal side of an aspartate residue. Enzyme pathways involved in detoxification of hydrogen peroxide, formaldehyde, and Sodium formate, which are produced as a consequence of oxidative demethylation by the cytochrome P-450 system, were examined in isolated hepatocytes from phenobarbital pretreated rats. The formaldehyde produced during oxidative demethylation in isolated hepatocytes is rapidly oxidized to Sodium formate. Depletion of cellular reduced glutathione by pretreatment of rats with diethylmaleate decreases the rate of Sodium formate production, and therefore, it appears that formaldehyde produced by oxidative demethylation is oxidized by formaldehyde dehydrogenase, an enzyme which requires but does not consume reduced glutathione. Because of the rapid nonenzymatic reaction of formaldehyde with reduced glutathione, this enzyme system may be viewed as essential to prevent the loss of reduced glutathione due to S-hydroxymethylglutathione formation. Reduced glutathione concentration in isolated hepatocytes decreased rapidly following addition of substrates undergoing oxidative demethylation. Addition of other cytochrome P-450 substrates which do not undergo demethylation did not result in such a dramatic oxidation of reduced glutathione. Sodium formate, produced during oxidative demethylation acts as a substrate for the peroxidatic mode of catalase, but also binds to catalase as an anionic ligand. This binding decreases the catalase concentration detectable by cyanide titration and therefore appears to inhibit the catalytic reaction mode. Synthesis of Sodium formate by hydrolysis of methyl formate is based on a two-stage process: in the first stage, methanol is carbonylated with carbon monoxide; in the second stage, methyl formate is hydrolyzed to Sodium formate and methanol. Sodium formate is produced as a byproduct in the liquid-phase oxidation of hydrocarbons to acetic acid. In the United States, butane is used as the hydrocarbon, and ca. 50 kg of Sodium formate is produced per ton of acetic acid. In Europe, the oxidation of naphtha is preferred, and up to 250 kg of Sodium formate is produced per ton of acetic acid in this process. The reaction of sodium formate or calcium formate with strong mineral acids, such as sulfuric and nitric acids, is the oldest known process for producing Sodium formate commercially. If formates or sodium hydroxide are available cheaply or occur as byproducts in other processes, Sodium formate can still be produced economically in this manner. A method for analysis of Sodium formate in concentration of approx 0.2 mg/l in body fluids and tissues is described. Formate dehydrogenase analysis is done in two steps. In the first step, a 0.1 ml sample of blood, urine, or tissue extraction is mixed with 0.1 of 10 mmol/l nicotinamide adenine dinucleotide soln, 0.1 ml of potassium phosphate buffer, and 50 ul of formate dehydrogenase soln. The mixture is incubated for 15 min at 37 °C then 0.1 ml of diaphorase soln, 50 ul of resazurin soln and 0.5 ml of phosphate buffer (pH 6.00, 200 mmol/l) are added. Fluorescence is measured. Indirect food substance additives affirmed as generally recognized as safe. (a) Sodium formate (CH2O2, CAS Reg. No. 64-18-6) is also referred to as methanoic acid or hydrogen carboxylic acid. It occurs naturally in some insects and is contained in the free acid state in a number of plants. Sodium formate is prepared by the reaction of sodium formate with sulfuric acid and is isolated by distillation. (b) Sodium formate is used as a constituent of paper and paperboard used for food packaging. (c) The ingredient is used at levels not to exceed good manufacturing practice in accordance with part 186.1(b)(1). (d) Prior sanctions for Sodium formate different from the uses established in this section do not exist or have been waived. An examination of 12 fatalities attributed to methanol poisoning is presented. Six individuals were found deceased, and their postmortem methanol and Sodium formate concentrations ranged from 84 to 543 mg/dL and 64 to 110 mg/dL, respectively. In the other six individuals, hospital treatment such as bicarbonate, ethanol infusion, and hemodialysis was administered. Antemortem methanol and Sodium formate concentrations ranged from 68 to 427 mg/dL and 37 to 91 mg/dL, respectively, whereas corresponding postmortem methanol and Sodium formate levels ranged from undetectable to 49 mg/dL and undetectable to 48 mg/dL, respectively. Hospital treatment of Sodium formate toxicity resulted in significantly reduced postmortem methanol and Sodium formate concentrations In 13-week studies, groups of 10 animals of each species and sex were exposed to Sodium formate at concentrations of 0, 8, 16, 32, 64, and 128 ppm for 6 hr a day, 5 days a week. Two mice, 1 male and 1 female, died in the 128 ppm groups. Body weight gains were significantly decreased in mice exposed to 64 and 128 ppm Sodium formate. Microscopic changes in rats and mice ranged from minimal to mild in severity and generally were limited to animals in the 128 ppm groups. Lesions related to exposure to Sodium formate consisted of squamous metaplasia and degeneration of the respiratory and olfactory epithelia, respectively. Hematologic and serum biochemical changes at interim and terminal time points were minimal to mild and, generally, were consistent with hemoconcentration. Sodium formate's production and use as a preservative in foods and silage; acidulant in dyeing of natural and synthetic fibers, leather tanning; coagulating latex in rubber production, and in chemical synthesis may result in its release to the environment through various waste streams. Its use in hydrofracking to prevent pipe corrosion and application to freshly cut grass prior to ensilation will result in its direct release to the environment. Sodium formate occurs in fruits, vegetables, and leaves and roots of plants, and also in the defensive secretions of numerous insects, particularly of ants. Sodium formate is an intermediary human metabolite that is immediately transformed to formate. If released to air, a vapor pressure of 42.6 mm Hg at 25 °C indicates Sodium formate will exist solely as a vapor in the atmosphere. Vapor-phase Sodium formate 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 36 days. Sodium formate does not absorb at wavelengths >290 nm and therefore is not expected to be susceptible to direct photolysis by sunlight. If released to soil, Sodium formate is expected to have very high mobility based upon an estimated Koc of 1. Volatilization from moist soil surfaces is expected to be an important fate process based upon a Henry's Law constant of 1.67X10-7 atm-cu m/mole. The pKa of Sodium formate is 3.75, indicating that this compound will primarily exist in anion form in the environment and anions generally do not adsorb more strongly to organic carbon and clay than their neutral counterparts. Sodium formate may volatilize from dry soil surfaces based upon its vapor pressure. Theoretical BOD values ranging from 4.3% to 77.6% after 5 days using sewage, activated sludge, fresh water, and synthetic sea water inocula indicate that biodegradation may be an important environmental fate process in soil and water. If released into water, Sodium formate is not 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 Henry's Law constant. Estimated volatilization half-lives for a model river and model lake are 150 and 1,100 days, respectively. An estimated BCF of 3.2 suggests the potential for bioconcentration in aquatic organisms is low. 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 Sodium formate may occur through inhalation and dermal contact with this compound at workplaces where Sodium formate is produced or used. Monitoring data indicate that the general population may be exposed to Sodium formate via inhalation of ambient air, ingestion of food, and dermal contact with this compound in consumer products containing Sodium formate as well as when stung by certain insects and marine cnidarians. Sodium formate occurs in fruits, vegetables, and leaves and roots of plants(1), and also in the defensive secretions of numerous insects, particularly of ants(2). It is also an intermediate product in the decomposition of organic matter in lake sediment(3) and a photooxidation product of alkanes, alkenes, and biogenic terpenes by hydroxyl-radical(4,5). Sodium formate is an intermediary human metabolite that is immediately transformed to formate(6). Based on a classification scheme(1), an estimated Koc value of 1(SRC), determined from a log Kow of -0.54(2) and a regression-derived equation(3), indicates that Sodium formate is expected to have very high mobility in soil(SRC). The pKa of Sodium formate is 3.75(4), indicating that this compound will primarily exist in anion form in the environment and anions generally do not adsorb more strongly to organic carbon and clay than their neutral counterparts(5). Volatilization of Sodium formate from moist soil surfaces is expected to be an important fate process(SRC) given a Henry's Law constant of 1.67X10-7 atm-cu m/mole(6). Sodium formate is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 42.6 mm Hg(7). Theoretical BOD values ranging from 4.3% to 77.6% after 5 days using sewage and activated sludge inocula(8-13) indicate that biodegradation may be an important environmental fate process in soil(SRC). According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), Sodium formate, which has a vapor pressure of 42.6 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase Sodium formate 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 36 days(SRC), calculated from its rate constant of 4.5X10-13 cu cm/molecule-sec at 25 °C(3). Sodium formate does not absorb at wavelengths >290 nm(4) and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC). Sodium formate biodegrades readily in screening tests(1-9). Specific results include: 4.3 and 38.8% of theoretical BOD after 5 and 10 days using a sewage inoculum(1); 43.7-77.6% of theoretical BOD after 5 days with a sewage inoculum(2); 70% of theoretical BOD in 24 hours using activated sludge(3); 66% of theoretical BOD in 12 hours using an activated sludge inoculum(4); 39.9% of theoretical BOD in 24 hours with activated sludge(5); 48 and 51% of theoretical BOD after 5 days with unacclimated and acclimated sewage inoculum, respectively(6); and 40.5 and 51.7% of theoretical BOD after 5 days with sewage inocula in fresh water and synthetic seawater, respectively(7). Microorganisms are present in the air that can degrade formate in rainwater(8). Sodium formate, present at 100 mg/L, reached 110% of its theoretical BOD in 2 weeks using an activated sludge inoculum at 30 mg/L in the Japanese MITI test(9). The rate constant for the vapor-phase reaction of Sodium formate with photochemically-produced hydroxyl radicals is 4.5X10-13 cu cm/molecule-sec at 25 °C(1). This corresponds to an atmospheric half-life of about 36 days at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(2). Sodium formate is not expected to undergo hydrolysis in the environment due to the lack of hydrolyzable functional groups(3). Sodium formate does not absorb at wavelengths >290 nm(4) and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC). The anhydrous acid catalyzes its own esterification with alcohols and polyols, but often also promotes dehydration to the ether or olefin(5). Anhydrous Sodium formate decomposes to carbon monoxide and water(6). Reactions between hydroxyl radicals and Sodium formate occur in cloud water. During daylight hours, aqueous-phase hydroxyl radical reactions can both produce and destroy Sodium formate in cloud drops and may control the Sodium formate levels in rain(7). The Koc of Sodium formate is estimated as 1(SRC), using a log Kow of -0.54(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that Sodium formate is expected to have very high mobility in soil. The pKa of Sodium formate is 3.75(4), indicating that this compound will primarily exist in anion form in the environment and anions generally do not adsorb more strongly to organic carbon and clay than their neutral counterparts(5). The Henry's Law constant for Sodium formate is 1.67X10-7 atm-cu m/mole(1). This Henry's Law constant indicates that Sodium formate is expected to volatilize from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 150 days(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 1100 days(SRC). Sodium formate's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of Sodium formate from dry soil surfaces may exist(SRC) based upon a vapor pressure of 42.6 mm Hg(3). Concentrations of Sodium formate in the Ohio River, Little Miami River and Tannes Creek were 12-39 ppb, 18.4-25.2 ppb, and 22.3 ppb, respectively(1). In Lake Kizaki in Japan, surface concentration of Sodium formate was 115 ppb(2). Although the concentration varied with depth (0-28 m) between 0 and 115 ppb, the variation was not a smoothly decreasing one(2). The volume-weighted average concentration of Sodium formate in Venezuelan rains was 7 uM in the continental region(1). Sodium formate was detected in 14 wet precipitation samples collected from 9 sites in southern California between 1982 and 1984 with concentrations ranging from 0.18 uM in snow from rural Wrightwood to 15.85 uM in rain from urban Los Angeles, and an average concentration of 4.12 uM(2). Six in-cloud precipitation samples collected from a cloud in Shenandoah National Park, VA during September 1990 had an average Sodium formate concentration of 8.3 uM(3). Precipitation samples collected at two Wisconsin lakes on the Wisconsin Acid Deposition Monitoring Network contained Sodium formate concentrations ranging from the detection limit of 20 ppb to 2,576 ppb, median 382 ppb(4). The average volume-weighted concentration of Sodium formate in rainwater in a study (154 measurements) at Wilmington, NC was 7.4 umol/L and contributed 19% of the rainwater's acidity(5). Fogwater in Corvallis, OR had a median and high Sodium formate concentration of 61 and 133 umol/L, respectively(6). NIOSH (NOES Survey 1981-1983) has statistically estimated that 158,933 workers (37,338 of these were female) were potentially exposed to Sodium formate in the US(1). The NOES Survey does not include farm workers. Occupational exposure to Sodium formate may occur through inhalation and dermal contact with this compound at workplaces where Sodium formate is produced or used(SRC). Monitoring data indicate that the general population may be exposed to Sodium formate via inhalation of ambient air, ingestion of food, and dermal contact with this compound in consumer products containing Sodium formate as well as when stung by certain insects and marine cnidarians(SRC). Sodium Formate is generally immediately available in most volumes. High purity, submicron and nanopowder forms may be considered. American Elements produces to many standard grades when applicable, including Mil Spec (military grade); ACS, Reagent and Technical Grade; Food, Agricultural and Pharmaceutical Grade; Optical Grade, USP and EP/BP (European Pharmacopoeia/British Pharmacopoeia) and follows applicable ASTM testing standards. Typical and custom packaging is available. Additional technical, research and safety (MSDS) information is available as is a Reference Calculator for converting relevant units of measurement. About Sodium formate Helpful information Sodium formate is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 100 000 to < 1 000 000 tonnes per annum. Sodium formate is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing. Consumer Uses Sodium formate is used in the following products: washing & cleaning products, polishes and waxes and water treatment chemicals. Other release to the environment of Sodium formate is likely to occur from: indoor use as processing aid. Article service life Other release to the environment of Sodium formate is likely to occur from: outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment). Sodium formate can be found in products with material based on: leather (e.g. gloves, shoes, purses, furniture) and metal (e.g. cutlery, pots, toys, jewellery). Widespread uses by professional workers Sodium formate is used in the following products: washing & cleaning products, laboratory chemicals, anti-freeze products and water treatment chemicals. Sodium formate is used in the following areas: mining, health services and municipal supply (e.g. electricity, steam, gas, water) and sewage treatment. Other release to the environment of Sodium formate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use. Formulation or re-packing Sodium formate is used in the following products: leather treatment products, laboratory chemicals and washing & cleaning products. Release to the environment of Sodium formate can occur from industrial use: formulation of mixtures, formulation in materials and of substances in closed systems with minimal release. Other release to the environment of Sodium formate is likely to occur from: indoor use as reactive substance. Uses at industrial sites Sodium formate is used in the following products: leather treatment products, heat transfer fluids, pH regulators and water treatment products and anti-freeze products. Sodium formate is used in the following areas: formulation of mixtures and/or re-packaging, mining and printing and recorded media reproduction. Sodium formate is used for the manufacture of: textile, leather or fur. Release to the environment of Sodium formate can occur from industrial use: in processing aids at industrial sites, in the production of articles, as processing aid, of substances in closed systems with minimal release, as an intermediate step in further manufacturing of another substance (use of intermediates) and formulation of mixtures. Other release to the environment of Sodium formate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners). Manufacture Release to the environment of Sodium formate can occur from industrial use: manufacturing of the substance and as an intermediate step in further manufacturing of another substance (use of intermediates).
SODIUM FUMARATE
cas no 527-07-1 D-Gluconic acid, sodium salt; D-Gluconic acid monosodium salt; Glonsen; Gluconato di sodio; Monosodium D-gluconate; Sodium (2R,3S,4R,5R')-2,3,4,5,6-pentahydroxyhexanoate; 2,3,4,5,6-Pentahydroxycaproic acid sodium salt; Sodium Gluconate;
SODIUM GLYCINATE
SODIUM GLYCOLATE, N° CAS : 2836-32-0 - Glycolate de sodium, Nom INCI : SODIUM GLYCOLATE, N° EINECS/ELINCS : 220-624-9, Ses fonctions (INCI), Régulateur de pH : Stabilise le pH des cosmétiques. Noms français : GLYCOLATE DE SODIUM. Noms anglais : ACETIC ACID, HYDROXY-, MONOSODIUM SALT; GLYCOLIC ACID, MONOSODIUM SALT; SODIUM .ALPHA.-HYDROXYACETATE; SODIUM GLYCOLATE
SODIUM GLYCOLATE ( Glycolate de sodium)
cas no 10124-56-8 Metaphosphoric acid, hexasodium salt; Calgon S; SHMP; Glassy sodium; Hexasodium metaphosphate; Metaphosphoric acid, hexasodium salt; Sodium Polymetaphosphate; sodium polymetaphosphate; Graham's Salt; Graham's salt; SHMP;
SODIUM HEXAMETAPHOSPHATE
Sodium Hexametaphosphate Uses of Sodium hexametaphosphate Sodium hexametaphosphate is used as a sequestrant and has applications within a wide variety of industries, including as a food additive in which Sodium hexametaphosphate is used under the E number E452i. Sodium carbonate is sometimes added to SHMP to raise the pH to 8.0–8.6, which produces a number of Sodium hexametaphosphate products used for water softening and detergents. A significant use for sodium hexametaphosphate is as a deflocculant in the production of clay-based ceramic particles. Sodium hexametaphosphate is also used as a dispersing agent to break down clay and other soil types for soil texture assessment. Sodium hexametaphosphate is used as an active ingredient in toothpastes as an anti-staining and tartar prevention ingredient. The energy drink NOS contains sodium hexametaphosphate. Food additive As a food additive, Sodium hexametaphosphate is used as an emulsifier. Artificial maple syrup, canned milk, cheese powders and dips, imitation cheese, whipped topping, packaged egg whites, roast beef, fish fillets, fruit jelly, frozen desserts, salad dressing, herring, breakfast cereal, ice cream, beer, and bottled drinks, among other foods, can contain Sodium hexametaphosphate. Preparation of Sodium hexametaphosphate Sodium hexametaphosphate is prepared by heating monosodium orthophosphate to generate sodium acid pyrophosphate: 2 NaH2PO4 → Na2H2P2O7 + H2O Subsequently, the pyrophosphate is heated to give the corresponding sodium hexametaphosphate: 3 Na2H2P2O7 → (NaPO3)6 + 3 H2O followed by rapid cooling. Reactions of Sodium hexametaphosphate SHMP hydrolyzes in aqueous solution, particularly under acidic conditions, to sodium trimetaphosphate and sodium orthophosphate. History of Sodium hexametaphosphate Hexametaphosphoric acid was named (but misidentified) in 1849 by the German chemist Theodor Fleitmann. By 1956, chromatographic analysis of hydrolysates of Graham's salt (sodium polyphosphate) indicated the presence of cyclic anions containing more than four phosphate groups; these findings were confirmed in 1961. In 1963, the German chemists Erich Thilo and Ulrich Schülke succeeded in preparing sodium hexametaphosphate by heating anhydrous sodium trimetaphosphate. Safety of Sodium hexametaphosphate Sodium phosphates are recognized to have low acute oral toxicity. Sodium hexametaphosphate concentrations not exceeding 10,000mg/l or mg/kg are considered protective levels by the EFSA and USFDA. Extreme concentrations of this salt may cause acute side effects from excessive blood serum concentrations of sodium, such as: “irregular pulse, bradycardia, and hypocalcemia." Properties of Sodium hexametaphosphate Chemical formula Na6P6O18 Molar mass 611.7704 g mol−1 Appearance White crystals Odor odorless Density 2.484 g/cm3 Melting point 628 °C (1,162 °F; 901 K) Boiling point 1,500 °C (2,730 °F; 1,770 K) Solubility in water soluble Solubility insoluble in organic solvents Refractive index (nD) 1.482 General description of Sodium hexametaphosphate Sodium hexametaphosphate is an inorganic polyphosphate salt commonly used as a corrosion inhibitor, emulsifying agent and as a tooth whitening agent in dentifrice formulations. Application of Sodium hexametaphosphate Sodium hexametaphosphate has been used as a deflocculant to prepare clay suspensions. Final report on the safety assessment of Sodium Metaphosphate, Sodium Trimetaphosphate, and Sodium Hexametaphosphate These inorganic polyphosphate salts all function as chelating agents in cosmetic formulations. In addition, Sodium Metaphosphate functions as an oral care agent, Sodium Trimetaphosphate as a buffering agent, and Sodium Hexametaphosphate as a corrosion inhibitor. Only Sodium Hexametaphosphate is currently reported to be used. Although the typical concentrations historically have been less than 1%, higher concentrations have been used in products such as bath oils, which are diluted during normal use. Sodium Metaphosphate is the general term for any polyphosphate salt with four or more phosphate units. The four-phosphate unit version is cyclic, others are straight chains. The hexametaphosphate is the specific six-chain length form. The trimetaphosphate structure is cyclic. Rats fed 10% Sodium Trimetaphosphate for a month exhibited transient tubular necrosis; rats given 10% Sodium Metaphosphate had retarded growth and those fed 10% Sodium Hexametaphosphate had pale and swollen kidneys. In chronic studies using animals, growth inhibition, increased kidney weights (with calcium deposition and desquamation), bone decalcification, parathyroid hypertrophy and hyperplasia, inorganic phosphaturia, hepatic focal necrosis, and muscle fiber size alterations. Sodium Hexametaphosphate was a severe skin irritant in rabbits, whereas a 0.2% solution was only mildly irritating. A similar pattern was seen with ocular toxicity. These ingredients were not genotoxic in bacterial systems nor were they carcinogenic in rats. No reproductive or developmental toxicity was seen in studies using rats exposed to Sodium Hexametaphosphate or Sodium Trimetaphosphate. In clinical testing, irritation is seen as a function of concentration; concentrations as high as 1% produced no irritation in contact allergy patients. Because of the corrosive nature of Sodium Hexametaphosphate, it was concluded that these ingredients could be used safely if each formulation was prepared to avoid skin irritation; for example, low concentration in a leave-on product or dilution of a higher concentration as part of product usage. Uses of Sodium hexametaphosphate Salt mixture of metaphosphates Great for combining with sodium citrate for making cheese sauces Commonly used as a pH buffer and sequestrant Cold/hot soluble, free flowing powder DESCRIPTION of Sodium hexametaphosphate (SHMP) 100% Pure Food Grade Sodium Hexametaphosphate SHMP (e452i) for use in molecular gastronomy. SHMP is a sequestrant, which allows gelling agents to be hydrated at much lower temperatures. It is the highest performing sequestrant available. And unlike sodium citrate, it has no taste at the concentrations used for gel hydration. OTHER DETAILS of Sodium hexametaphosphate Dietary Attributes: Plant-Based, Gluten-Free, Non-GMO, Kosher (OU), Keto-friendly Ingredient List: Sodium Hexametaphosphate Allergen(s): None Effect of sodium hexametaphosphate concentration and cooking time on the physicochemical properties of pasteurized process cheese Sodium hexametaphosphate (SHMP) is commonly used as an emulsifying salt (ES) in process cheese, although rarely as the sole ES. It appears that no published studies exist on the effect of Sodium hexametaphosphate concentration on the properties of process cheese when pH is kept constant; pH is well known to affect process cheese functionality. The detailed interactions between the added phosphate, casein (CN), and indigenous Ca phosphate are poorly understood. We studied the effect of the concentration of Sodium hexametaphosphate (0.25–2.75%) and holding time (0–20 min) on the textural and rheological properties of pasteurized process Cheddar cheese using a central composite rotatable design. All cheeses were adjusted to pH 5.6. The meltability of process cheese (as indicated by the decrease in loss tangent parameter from small amplitude oscillatory rheology, degree of flow, and melt area from the Schreiber test) decreased with an increase in the concentration of Sodium hexametaphosphate. Holding time also led to a slight reduction in meltability. Hardness of process cheese increased as the concentration of Sodium hexametaphosphate increased. Acid-base titration curves indicated that the buffering peak at pH 4.8, which is attributable to residual colloidal Ca phosphate, was shifted to lower pH values with increasing concentration of Sodium hexametaphosphate. The insoluble Ca and total and insoluble P contents increased as concentration of Sodium hexametaphosphate increased. The proportion of insoluble P as a percentage of total (indigenous and added) P decreased with an increase in ES concentration because of some of the (added) Sodium hexametaphosphate formed soluble salts. The results of this study suggest that Sodium hexametaphosphate chelated the residual colloidal Ca phosphate content and dispersed CN; the newly formed Ca-phosphate complex remained trapped within the process cheese matrix, probably by cross-linking CN. Increasing the concentration of Sodium hexametaphosphate helped to improve fat emulsification and CN dispersion during cooking, both of which probably helped to reinforce the structure of process cheese. Process cheese is made by grinding natural cheese and then heating the cheese in the presence of one or more Ca chelating salts (phosphate or citrates), often called emulsifying salts (ES). In the United States, the Code of Federal Regulations (Department of Health and Human Services, 2004) identifies 13 types of ES that can be used in process cheese manufacture, either singly or in combination, and allows for the addition of up to 3% (wt/wt; Kapoor and Metzger, 2008). These ES help disperse the insoluble CN in natural cheese curd, and it is these solubilized CN that can then act as emulsifiers around the liquid fat released during the heating and shearing of natural cheese. These ES function as ion exchangers, buffers, and Ca sequestrants and cause CN dispersion and peptization. Several reviews exist on the properties of the ES used for process cheese manufacture (Carić et al., 1985; Berger et al., 1998; Zehren and Nusbaum, 2000; Guinee et al., 2004). Long-chain polyphosphates are commonly (but incorrectly) called hexametaphosphates. The real hexametaphosphates are ring forming and are not used in process cheese. Sodium hexametaphosphates (SHMP) have a wide range of uses in the food industry, including increasing the water binding properties of proteins in processed meats, protein precipitation for purification purposes, and prevention of protein sedimentation in sterilized milks (Molins, 1991). Sodium hexametaphosphates are often used in process cheese manufacture either singly or more commonly in a blend of several types of ES. Numerous factors, including pH, affect the melting and textural characteristics of process cheese (Mulsow et al., 2007). Many of these factors, which are not well understood at the molecular level, are interrelated and have a combined effect on meltability and texture. It has been reported that the use of Sodium hexametaphosphate produces hard and poorly meltable process cheese (Thomas, 1973; Gupta et al., 1984; Carić et al., 1985). However, it appears that no studies exist on the effect of Sodium hexametaphosphate on process cheese properties where pH was kept constant (to avoid pH as a confounding factor). Gupta et al. (1984) reported that the use of Sodium hexametaphosphate resulted in process cheese with low pH values, which could have contributed to the poor textural attributes. Lu et al. (2008) reported that increasing the pH resulted in improved meltability for process cheese made with Sodium hexametaphosphate. Cooking time also affects the properties of process cheese (Rayan et al., 1980; Shirashoji et al., 2006). One method by which cooking time affects process cheese is by increasing the extent of shearing of curd and thus improving the emulsification of fat (i.e., by reducing the size of emulsified fat globules; Shimp, 1985; Kapoor and Metzger, 2008). The objective of this study was to investigate the effects of various concentrations of Sodium hexametaphosphate and cooking times on the rheological and textural properties of process cheese. Because pH is well known to influence the texture of process cheese made with Sodium hexametaphosphate (Lu et al., 2008), all samples were adjusted to a constant pH value (∼5.6). Rheological Properties of Sodium hexametaphosphate The effects of ES concentration on the rheological properties of process cheese made with Sodium hexametaphosphate during heating are shown in Figures 1a and b. The rheological properties of the natural Cheddar cheese are also shown for comparison purposes. The G′ value of all cheeses decreased with temperature from 5 to 70°C. The G′ value of the process cheese made with 1.50 and 2.75% ES, as well as natural cheese, increased again at >70°C, although cheese made with 0.25% ES continued to decrease with increasing temperature throughout the entire heating range. This increase in G′ at high temperature was not observed with any of the process cheeses made with trisodium citrate (TSC) in our previous study (Shirashoji et al., 2006). The LT value of process cheese measured at >50°C decreased with an increase in ES concentration. Process cheese made with 2.75% Sodium hexametaphosphate had LT values that were <1 over the entire heating range. Samples with LT values <1 do not exhibit flow (Lucey et al., 2003). Several factors could explain the effect of increasing Sodium hexametaphosphate concentration on cheese texture. Increasing the concentration of Sodium hexametaphosphate (SHMP) used in process cheese resulted in an increase in hardness and the G′ value at 70°C and a decrease in the LT value at 50°C and DOF. These effects were not attributable to any compositional factors because we manufactured the cheeses to a constant composition. We believe that the higher hardness and lower meltability with increasing Sodium hexametaphosphate concentration is attributable to a combination of enhanced CN dispersion, Ca chelation, and ion exchange. One of the key functions of ES, such as Sodium hexametaphosphate, is the ability to disperse (sometimes called peptization) the insoluble CN matrix in natural cheese. Polyphosphates have a greater CN dispersing ability compared with orthophosphates or TSC (Lee et al., 1986; Molins, 1991; Dimitreli et al., 2005; Mizuno and Lucey, 2005). The addition of Sodium hexametaphosphate to milk rapidly causes CN dispersion (Vujicic et al., 1968). The use of Sodium hexametaphosphate in process cheese greatly increases CN dispersion (hydration, peptization, or swelling) compared with TSC or orthophosphates (Lee et al., 1986; Guinee et al., 2004), although in these studies the pH of cheese was not kept constant. Increasing the concentration of polyphosphate used in process cheese resulted in an increase in soluble nitrogen content (indicating greater CN dispersion; Lee and Alais, 1980). Hot process cheese after holding at 80°C for 10 min exhibited very large LT values compared with process cheeses made with low ES concentration. The high LT values in hot process cheese made with high ES concentrations suggest that increasing the concentration of Sodium hexametaphosphate greatly increased CN dispersion. The ability of Sodium hexametaphosphate to disperse CN is pH-dependent with low ability near pH 5 (Dimitreli et al., 2005). Our cheeses were all at pH 5.6, and at this pH value Sodium hexametaphosphate should still be effective at causing CN dispersion. These highly dispersed CN molecules then reassociate during cooling to form a fine-structured gel network (some CN reassociation may be occurring in the hot product as evidenced by the increase in G′ values during the holding of cheese at 80°C). The greater the degree of CN dispersion, the firmer, more cross-linked, and less meltable is the final process cheese. This agrees with the similar trend reported for process cheese made with increasing concentrations of TSC (Shirashoji et al., 2006). Johnston and Murphy (1992) reported that there was greater CN dispersion in milk with an increase in Sodium hexametaphosphate levels; acid gels made from these Sodium hexametaphosphate-treated milks had improved gel textural properties. Polyphosphates also have a strong ability to complex Ca, and we can rank phosphates and citrates in the following order: long-chain phosphates > tripolyphosphate > pyrophosphate > citrate > orthophosphate (Van Wazer and Callis, 1958). The strong Ca binding properties of Sodium hexametaphosphate should result in greater dispersion of CN because of the loss of CCP cross-links present in natural cheese. The highly charged anionic nature of polyphosphates causes them to be attracted to the oppositely charged groups on other long-chain polyelectrolytes, such as proteins (Van Wazer and Callis, 1958). In our process cheeses, association of polyphosphate with CN should increase the charge repulsion between CN molecules. In some circumstances the addition of phosphates to milk can cause gelation (Mizuno and Lucey, 2007). Sodium hexametaphosphate was less effective at gelling CN than tetrasodium pyrophosphate. One factor that inhibits gelation of CN is that polyphosphates introduce more charge repulsion to CN because of their multiple negative charges (i.e., polyelectrolyte nature) compared with tetrasodium pyrophosphate. Another possible factor that could contribute to the increased hardness and reduced meltability of cheese made with high concentration of Sodium hexametaphosphate (SHMP) is the formation of new Ca phosphate linkages within the cheese network (Gupta et al., 1984). Taneya et al. (1980) reported that long protein strands were observed in a process cheese made with sodium polyphosphate, whereas these long strands were not observed in a process cheese made with TSC. Long CN strands in process cheese could have resulted from the formation of new Ca phosphate linkages between CN. The insoluble Ca and insoluble P content (Table 3) of process cheese increased with increasing Sodium hexametaphosphate concentration. The addition of Sodium hexametaphosphate to milk protein concentrate at pH 5.8 increased CN-bound Ca (Mizuno and Lucey, 2005). Polyphosphates bind Ca from the native CCP (which help to disperse the CN micelles), but these new Ca phosphates complexes can associate with the dispersed CN (Odagiri and Nickerson, 1965; Mizuno and Lucey, 2005). Lee and Alais (1980) reported that the use of polyphosphates resulted in a high level of insoluble P in process cheese. Johnston and Murphy (1992) reported that skim milk solutions with polyphosphate contained a high proportion of nonsedimentable (soluble) CN. Apart from the lowest ES concentration, all other process cheese samples exhibited an increase in G′ at temperatures >70°C during heating. Udayarajan et al. (2005) suggested that the increase in G′ value of natural Cheddar cheese at high temperature was attributable to the heat-induced formation of additional Ca phosphate cross-links between CN. The acid-base buffering profiles of process cheese indicate that the addition of Sodium hexametaphosphate caused a shift in the pH value where the buffering peak occurred during acidification. Lucey et al. (1993) suggested that a change in location or shape of the buffering peak observed during the acidification of milk might be attributable to some shift in the structure, or composition, or both, of the indigenous CCP. The buffering profiles of process cheese suggest that increasing the Sodium hexametaphosphate content altered the type and concentration of Ca phosphate salts present in the cheese network. A small quantity of Sodium hexametaphosphate (0.25%) was not enough to efficiently disperse the CN network even with the use of long holding times during the cooking step. Consequently, fat was poorly emulsified (results not shown) and the process cheese was relatively soft and had good meltability. Holding time resulted in a significant decrease in the LT value at 50°C, DOF, and Schreiber melt area and a significant increase in hardness and the G′ value at 70°C. Long holding times have previously been reported to reduce melt and increase hardness of process cheese (Rayan et al., 1980). An increase in the hold time also increases the extent of shear applied to the process cheese; this creates smaller homogenized fat globules that reinforce the matrix formed during cooling. During prolonged holding time at high temperatures, it is likely that some heat-induced CN aggregation occurred. Although increasing the concentration of ES used in process cheese resulted in an increase in the initial measured LT of the hot product (i.e., measured after a holding time of 10 min at 80°C), during (further) prolonged holding there was a substantial decrease in the LT and an increase in G′ values. Panouillé et al. (2003) observed that heat-induced aggregation and gelation of CN micelles could occur in the presence of sodium polyphosphates. Holding time had no significant effect on the insoluble Ca or P content. Because Sodium hexametaphosphate is a very effective Ca chelating agent, the time required to heat the process cheese to 80°C was likely sufficient to allow Sodium hexametaphosphate to chelate Ca from CN (i.e., a holding time at 80°C was not required to facilitate Ca chelation). In solution, polyphosphates can undergo hydrolysis to orthophosphates, particularly at higher temperatures (>60°C; Maurer-Rothmann and Scheurer, 2005). In practice, Sodium hexametaphosphate (SHMP) is likely that the hydrolytic breakdown is low in most process cheese applications (Maurer-Rothmann and Scheurer, 2005). During holding of process cheese at high temperature some hydrolysis of Sodium hexametaphosphate may have occurred (Lee and Alais, 1980); however, holding time had no significant effect on the concentration of insoluble P in process cheese. It has been claimed (Roesler, 1966) that hydrolysis also occurs in process cheese during storage. Because the process cheese samples were not analyzed until after 7 d of storage, any (possible) hydrolysis should already have occurred before testing of cheese. Comparing the results reported by Shirashoji et al. (2006) for process cheese made with TSC to those made with Sodium hexametaphosphate in the present study, we observed that cheese made with Sodium hexametaphosphate had lower LT values at 50°C and lower DOF values for all experimental conditions. The experimental work for our previous study (Shirashoji et al., 2006) was actually performed around the same time period as the current study. The hardness values for process cheese made with various concentrations of TSC were much lower (range: 1,572–2,685 g; Shirashoji et al., 2006) compared with cheese made with Sodium hexametaphosphate (range: 1,892–4,490 g). Conclusions The concentration of Sodium hexametaphosphate used as an ES in the manufacture of pasteurized process Cheddar cheese greatly affected the textural and melting properties, even when these cheeses had a similar pH value. The added Sodium hexametaphosphate appeared to convert the original form of CCP to a new type of Ca phosphate salt during cooking. A small quantity of Sodium hexametaphosphate (0.25%) was not enough to efficiently disperse the CN network even with long holding times during cooking; consequently, fat was poorly emulsified and the process cheese was soft and highly meltable. Holding times increased hardness and decreased meltability. High levels of Sodium hexametaphosphate produced firm and poorly meltable cheese because CN were highly dispersed during cooking, Sodium hexametaphosphate resulted in the formation of new Ca phosphate-CN linkages, and a fine-stranded network was formed during cooling. The results of this study will assist process cheese manufacturers in understanding the role of Sodium hexametaphosphate as an ES and demonstrates the effect of ES concentration and holding time on process cheese functionality. Sodium hexametaphosphate (SHMP) Chemical Properties,Uses,Production Outline Sodium hexametaphosphate is a kind of sodium metaphosphate polymers. Sodium hexametaphosphate is also known as "polyvinylidene sodium," "sodium multiple metaphosphate", "sodium metaphosphate vitreous body", and "Graham salt". Sodium hexametaphosphate is a colorless transparent glass-like solid or white powder with greater solubility but low dissolving rate in water. Its aqueous solution exhibits acidic property. Its complex of divalent metal ion is relatively more stable than the complexes of mono-valent metal ion. Sodium hexametaphosphate can easily be hydrolyzed to orthophosphate in warm water, acid or alkali solution. Hexametaphosphate has a relative strong hygroscopicity with being sticky after absorbing moisture. For certain metal ions (e.g., calcium, magnesium, etc.), it has the ability to form soluble complexes, and thus being able to being used for demineralizing water. Sodium hexametaphosphate can also from precipitate with lead and silver ions with precipitate being re-dissolved in excess amount of sodium hexametaphosphate solution to form a complex salt. Its barium salt can also form complexes with the sodium hexametaphosphate. Sodium hexametaphosphate can be used as a kind of highly efficient water softener of power stations, rolling stock boiler water; as detergent additive, as corrosion-controlling or anti-corrosion agents; as cement hardening accelerator; as streptomycin purification agent, and the cleaning agent of textile industry and dyeing industry. Sodium hexametaphosphate can also be used as a kind of sedative drug, preservative, stabilizer, and fruit juice precipitant in food industry. In the oil industry, it is used for control of drilling pipe rust and adjusting the viscosity of oil drilling mud. Sodium hexametaphosphate also has applications in fabric dyeing, tanning, paper, color film, soil analysis, radiation chemistry and analytical chemistry and other departments. Our GB2760-1996 provisions that hexametaphosphate is allowable food additives (water retention agent) for being used for canned food, fruit juice drinks, dairy products, soy products; it can also be used as a dye dispersant, and water treatment agent. Toxicity of Sodium hexametaphosphate Adl 0~70 mg/kg (in terms of phosphorus); LD50:4g/kg (rat, oral). According to the provision of the GB2760-86, it is allowed for being applied to canned food, fruit juice drinks, dairy products, soy milk as quality improver; the maximum usage amount is 1.0 g/kg. When being used as composite phosphate, calculated as the total phosphate, the canned meat products shall not exceed 1.0 g/kg; for condensation of milk, it shall not exceed 0.50 g/kg. Chemical Properties of Sodium hexametaphosphate Sodium hexametaphosphate is colorless and transparent glass flake or white granular crystals. It is easily soluble in water but insoluble in organic solvents. Uses of Sodium hexametaphosphate Sodium hexametaphosphate can be used as a food quality improver in food industry, pH adjusting agent, metal ion chelating agents, dispersants, extenders, etc. Sodium hexametaphosphate can be used as a kind of common analytical reagents, water softener, and also used for photofinishing and printing. Sodium hexametaphosphate can be used as a water softener, detergent, preservative, cement hardening accelerator, fiber dyeing and cleaning agents; it can also used for medicine, food, petroleum, printing and dyeing, tanning, and paper industry. Sodium hexametaphosphate can be used as texturizing agent; emulsifiers; stabilizer; chelating agent. Sodium hexametaphosphate is less frequently for being used alone and is generally used in mixture with pyrophosphate and metaphosphate. The mixture is mainly used for ham, sausage, surimi such as the tissue improver for water retention, tendering and meat softening. It can also be used for prevention of crystallization of canned crab as well as dissolving agent of pectin. Sodium hexametaphosphate can be used as the water softening agent of boiler water and industrial water (including water for the production of dyes, water for the production of titanium dioxide, water for printing and dyeing, and slurry mixing, water for cleaning color copy of the film, as well as chemical industrial water and the water for the medicines, reagents production, etc.) as well as the water treatment agent for the industrial cooling water; it can also be used as a corrosion inhibitor, flotation agent, dispersant agent, high temperature binding agent, dyeing auxiliaries, metal surface treatment, rust inhibitors, detergent additives and also cement hardening accelerator. Coated paper production can use it as pulp dispersants in order to improve the penetration capability. In addition, it can also be apply to the washing utensils and chemical fiber in order to remove iron ions of the pulp. In the oil industry, it can be used for the antirust of the drilling pipe and adjusting the slurry viscosity upon the control of oil drilling. Sodium hexametaphosphate can be used as the quality improver with various effects of increasing the complex metal ions of food, pH, ionic strength, thereby improving the adhesive capability as well as the water holding ability of food. China provides that it can be applied to the dairy products, poultry products, ice cream, instant noodles and meat with the maximum permitted amount being 5.0 g/kg; the maximal permitted usage amount in canned food, fruit juice (flavored) drinks and vegetable protein drink is 1.0g/kg. Sodium hexametaphosphate can be used as a food quality improver in food industry and applied to canned food, fruit juice drinks, dairy products, and soy milk. Sodium hexametaphosphate can be used as Ph adjusting agent, metal ion chelate agent, adhesive and bulking agents. When being applied to beans and canned fruits and vegetables, it can be stabilize the natural pigment and protect the food color and lustre; when being used in canned meat, it can be used for preventing the emulsification of the fat and maintaining its uniform texture; when being applied to meat, it can be used to increase the water holding capacity and prevent the deterioration of fat in the meat. Sodium hexametaphosphate can also help to clarify the wine when being supplied to beer and further prevent turbidity. Chemical Properties of Sodium hexametaphosphate The sodium polyphosphates class consists of several amorphous, water soluble polyphosphates composed of linear chains of metaphosphate units, (NaPO3)x where x ≥ 2, terminated by Na2PO4- groups. They are usually identified by their Na2O/ P2O5 ratio or their P2O5 content. The Na2O/P2O5 ratios vary from about 1.3 for sodium tetrapolyphosphate, where x = approximately 4; through about 1.1 for Graham’s salt, commonly called sodium hexametaphosphate, where x = 13 to 18; to about 1.0 for the higher molecular weight sodium polyphosphates, where x = 20 to 100 or more. The pH of their solution varies from about 3 to 9. For additional details of description, refer to Burdock (1997). Uses of Sodium hexametaphosphate Sodium Hexametaphosphate is a sequestrant and moisture binder that is very soluble in water but dissolves slowly. solutions have a ph of 7.0. Sodium hexametaphosphate permits peanuts to be salted in the shell by making it possible for the salt brine to penetrate the peanuts. in canned peas and lima beans, Sodium hexametaphosphate functions as a tenderizer when added to the water used to soak or scald the vegetables prior to canning. Sodium hexametaphosphate improves whipping properties in whipping proteins. Sodium hexametaphosphate functions as a seques- trant for calcium and magnesium, having the best sequestering power of all the phosphates. it prevents gel formation in sterilized milk. it is also termed sodium metaphosphate and graham’s salt. Uses For industrial use, such as oil field, paper-making, textile, dyeing, petrochemical industry,tanning industry, metallurgical industry and building material industry, It is mainly used as a water sortening agent in solution for printing, dyeing ,and boiler; Diffusant in papermersing medium, high temperature agglomerant,detergent and soil analytical chemistry reagent, Uses sodium hexametaphosphate is a chelating agent and a corrosion inhibitor. This is an inorganic salt. Preparation of Sodium hexametaphosphate Sodium hexametaphosphate is prepared by heating monosodium phosphate (NaH2PO4) rapidly to a clear melt, which occurs slightly above 625°C. Rapid chilling of this melt produces a very soluble glass, which is then crushed or milled. Agricultural Uses of Sodium hexametaphosphate Sodium metaphosphate is the salt of metaphosphoric acid having a molecular formula (NaPO3)n, where n ranges from 3 to 10 (for cyclic molecules) or may be much larger (for polymers).
SODIUM HUMATE
SODIUM HYDROSULFITE, N° CAS : 7775-14-6, Nom INCI : SODIUM HYDROSULFITE, Nom chimique : Sodium dithionite, N° EINECS/ELINCS : 231-890-0. Ses fonctions (INCI), Agent réducteur : Modifie la nature chimique d'une autre substance en ajoutant de l'hydrogène ou en éliminant l'oxygène. Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques
SODIUM HYDROXIDE
SYNONYMS Caustic soda; Sodium hydrate; soda lye; Lye;White Caustic CAS NO. 1310-73-2
SODIUM HYDROXIDE
IUPAC name: Sodium hydroxide
CAS Number: 1310-73-2
EC Number: 215-185-5
Chemical formula: NaOH
Molar mass: 39.9971 g/mol

Sodium hydroxide, also known as lye and caustic soda, is an inorganic compound with the formula NaOH.
Sodium hydroxide is a white solid ionic compound consisting of sodium cations Na+ and hydroxide anions OH−.

Sodium hydroxide is a highly caustic base and alkali that decomposes proteins at ordinary ambient temperatures and may cause severe chemical burns.
Sodium hydroxide is highly soluble in water, and readily absorbs moisture and carbon dioxide from the air.
Sodium hydroxide forms a series of hydrates NaOH·nH2O.

The monohydrate NaOH·H2O crystallizes from water solutions between 12.3 and 61.8 °C.
The commercially available "sodium hydroxide" is often this monohydrate, and published data may refer to it instead of the anhydrous compound.

As one of the simplest hydroxides, sodium hydroxide is frequently used alongside neutral water and acidic hydrochloric acid to demonstrate the pH scale to chemistry students.

Sodium hydroxide is used in many industries: in the manufacture of pulp and paper, textiles, drinking water, soaps and detergents, and as a drain cleaner.
Worldwide production in 2004 was approximately 60 million tons, while demand was 51 million tons.

Properties
Physical properties
Pure sodium hydroxide is a colorless crystalline solid that melts at 318 °C (604 °F) without decomposition, and with a boiling point of 1,388 °C (2,530 °F).
Sodium hydroxide is highly soluble in water, with a lower solubility in polar solvents such as ethanol and methanol.
NaOH is insoluble in ether and other non-polar solvents.

Similar to the hydration of sulfuric acid, dissolution of solid sodium hydroxide in water is a highly exothermic reaction where a large amount of heat is liberated, posing a threat to safety through the possibility of splashing.

The resulting solution is usually colorless and odorless.
As with other alkaline solutions, it feels slippery with skin contact due to the process of saponification that occurs between NaOH and natural skin oils.

Viscosity
Concentrated (50%) aqueous solutions of sodium hydroxide have a characteristic viscosity, 78 mPa·s, that is much greater than that of water (1.0 mPa·s) and near that of olive oil (85 mPa·s) at room temperature.
The viscosity of aqueous NaOH, as with any liquid chemical, is inversely related to its service temperature, i.e., its viscosity decreases as temperature increases, and vice versa.
The viscosity of sodium hydroxide solutions plays a direct role in its application as well as its storage.

Hydrates
Sodium hydroxide can form several hydrates NaOH·nH2O, which result in a complex solubility diagram that was described in detail by S.U. Pickering in 1893.
The known hydrates and the approximate ranges of temperature and concentration (mass percent of NaOH) of their saturated water solutions are:

Heptahydrate, NaOH·7H2O: from −28 °C (18.8%) to −24 °C (22.2%).
Pentahydrate, NaOH·5H2O: from −24 °C (22.2%) to −17.7 (24.8%).
Tetrahydrate, NaOH·4H2O, α form: from −17.7 (24.8%) to +5.4 °C (32.5%).
Tetrahydrate, NaOH·4H2O, β form: metastable.
Trihemihydrate, NaOH·3.5H2O: from +5.4 °C (32.5%) to +15.38 °C (38.8%) and then to +5.0 °C (45.7%).
Trihydrate, NaOH·3H2O: metastable.
Dihydrate, NaOH·2H2O: from +5.0 °C (45.7%) to +12.3 °C (51%).
Monohydrate, NaOH·H2O: from +12.3 °C (51%) to 65.10 °C (69%) then to 62.63 °C (73.1%).
Early reports refer to hydrates with n = 0.5 or n = 2/3, but later careful investigations failed to confirm their existence.

The only hydrates with stable melting points are NaOH·H2O (65.10 °C) and NaOH·3.5H2O (15.38 °C).
The other hydrates, except the metastable ones NaOH·3H2O and NaOH·4H2O (β) can be crystallized from solutions of the proper composition, as listed above.

However, solutions of NaOH can be easily supercooled by many degrees, which allows the formation of hydrates (including the metastable ones) from solutions with different concentrations.

For example, when a solution of NaOH and water with 1:2 mole ratio (52.6% NaOH by mass) is cooled, the monohydrate normally starts to crystallize (at about 22 °C) before the dihydrate.
However, the solution can easily be supercooled down to −15 °C, at which point it may quickly crystallize as the dihydrate.

When heated, the solid dihydrate might melt directly into a solution at 13.35 °C; however, once the temperature exceeds 12.58 °C.
Sodium hydroxide often decomposes into solid monohydrate and a liquid solution.
Even the n = 3.5 hydrate is difficult to crystallize, because the solution supercools so much that other hydrates become more stable.

A hot water solution containing 73.1% (mass) of NaOH is an eutectic that solidifies at about 62.63 °C as an intimate mix of anhydrous and monohydrate crystals.

A second stable eutectic composition is 45.4% (mass) of NaOH, that solidifies at about 4.9 °C into a mixture of crystals of the dihydrate and of the 3.5-hydrate.

The third stable eutectic has 18.4% (mass) of NaOH. Sodium hydroxide solidifies at about −28.7 °C as a mixture of water ice and the heptahydrate NaOH·7H2O.

When solutions with less than 18.4% NaOH are cooled, water ice crystallizes first, leaving the NaOH in solution.

The α form of the tetrahydrate has density 1.33 g/cm3. Sodium hydroxide melts congruously at 7.55 °C into a liquid with 35.7% NaOH and density 1.392 g/cm3, and therefore floats on it like ice on water. However, at about 4.9 °C it may instead melt incongruously into a mixture of solid NaOH·3.5H2O and a liquid solution.

The β form of the tetrahydrate is metastable, and often transforms spontaneously to the α form when cooled below −20 °C.[17] Once initiated, the exothermic transformation is complete in a few minutes, with a 6.5% increase in volume of the solid. The β form can be crystallized from supercooled solutions at −26 °C, and melts partially at −1.83 °C.

The "sodium hydroxide" of commerce is often the monohydrate (density 1.829 g/cm3). Physical data in technical literature may refer to this form, rather than the anhydrous compound.

Crystal structure
NaOH and its monohydrate form orthorhombic crystals with the space groups Cmcm (oS8) and Pbca (oP24), respectively.
The monohydrate cell dimensions are a = 1.1825, b = 0.6213, c = 0.6069 nm.
The atoms are arranged in a hydrargillite-like layer structure /O Na O O Na O/...

Each sodium atom is surrounded by six oxygen atoms, three each from hydroxyl anions HO− and three from water molecules.
The hydrogen atoms of the hydroxyls form strong bonds with oxygen atoms within each O layer.
Adjacent O layers are held together by hydrogen bonds between water molecules.

Chemical properties
Reaction with acids
Sodium hydroxide reacts with protic acids to produce water and the corresponding salts.
For example, when sodium hydroxide reacts with hydrochloric acid, sodium chloride is formed:

NaOH(aq) + HCl(aq) → NaCl(aq) +H2O(l)
In general, such neutralization reactions are represented by one simple net ionic equation:

OH−(aq) + H+(aq) → H2O(l)
This type of reaction with a strong acid releases heat, and hence is exothermic.
Such acid–base reactions can also be used for titrations. However, sodium hydroxide is not used as a primary standard because it is hygroscopic and absorbs carbon dioxide from air.

Reaction with acidic oxides
Sodium hydroxide also reacts with acidic oxides, such as sulfur dioxide.
Such reactions are often used to "scrub" harmful acidic gases (like SO2 and H2S) produced in the burning of coal and thus prevent their release into the atmosphere.
For example,

2 NaOH + SO2 → Na2SO3 + H2O
Reaction with metals and oxides
Glass reacts slowly with aqueous sodium hydroxide solutions at ambient temperatures to form soluble silicates.
Because of this, glass joints and stopcocks exposed to sodium hydroxide have a tendency to "freeze".

Flasks and glass-lined chemical reactors are damaged by long exposure to hot sodium hydroxide, which also frosts the glass. Sodium hydroxide does not attack iron at room temperatures, since iron does not have amphoteric properties (i.e., it only dissolves in acid, not base).

Nevertheless, at high temperatures (e.g. above 500 °C), iron can react endothermically with sodium hydroxide to form iron(III) oxide, sodium metal, and hydrogen gas.

This is due to the lower enthalpy of formation of iron(III) oxide (−824.2 kJ/mol) compared to sodium hydroxide (-500 kJ/mol) and positive entropy change of reaction, which imply spontaneity at high temperatures (ΔST>ΔH, ΔG<0) and non-spontaneity at low temperatures (ΔST<ΔH, ΔG>0).
Consider the following reaction between molten sodium hydroxide and finely divided iron filings:

4 Fe + 6 NaOH → 2 Fe2O3 + 6 Na + 3 H2
A few transition metals, however, may react vigorously with sodium hydroxide under milder conditions.

In 1986, an aluminium road tanker in the UK was mistakenly used to transport 25% sodium hydroxide solution, causing pressurization of the contents and damage to the tanker.
The pressurization was due to the hydrogen gas which is produced in the reaction between sodium hydroxide and aluminium:

2 Al + 2 NaOH + 6 H2O → 2 NaAl(OH)4 + 3 H2

Precipitant
Unlike sodium hydroxide, which is soluble, the hydroxides of most transition metals are insoluble, and therefore sodium hydroxide can be used to precipitate transition metal hydroxides. The following colours are observed:

Copper - blue
Iron(II) - green
Iron(III) - yellow / brown
Zinc and lead salts dissolve in excess sodium hydroxide to give a clear solution of Na2ZnO2 or Na2PbO2.

Aluminium hydroxide is used as a gelatinous flocculant to filter out particulate matter in water treatment. Aluminium hydroxide is prepared at the treatment plant from aluminium sulfate by reacting it with sodium hydroxide or bicarbonate.

Al2(SO4)3 + 6 NaOH → 2 Al(OH)3 + 3 Na2SO4
Al2(SO4)3 + 6 NaHCO3 → 2 Al(OH)3 + 3 Na2SO4 + 6 CO2

Saponification
Sodium hydroxide can be used for the base-driven hydrolysis of esters (as in saponification), amides and alkyl halides.
However, the limited solubility of sodium hydroxide in organic solvents means that the more soluble potassium hydroxide (KOH) is often preferred.
Touching a sodium hydroxide solution with bare hands, while not recommended, produces a slippery feeling.

This happens because oils on the skin such as sebum are converted to soap.
Despite solubility in propylene glycol it is unlikely to replace water in saponification due to propylene glycol's primary reaction with fat before reaction between sodium hydroxide and fat.

Production
For historical information, see Alkali manufacture.
Sodium hydroxide is industrially produced as a 50% solution by variations of the electrolytic chloralkali process.

Chlorine gas is also produced in this process.
Solid sodium hydroxide is obtained from this solution by the evaporation of water.
Solid sodium hydroxide is most commonly sold as flakes, prills, and cast blocks.

In 2004, world production was estimated at 60 million dry tonnes of sodium hydroxide, and demand was estimated at 51 million tonnes.
In 1998, total world production was around 45 million tonnes.
North America and Asia each contributed around 14 million tonnes, while Europe produced around 10 million tonnes.

In the United States, the major producer of sodium hydroxide is Olin, which has annual production around 5.7 million tonnes from sites at Freeport, Texas, and Plaquemine, Louisiana, St Gabriel, Louisiana, McIntosh, Alabama, Charleston, Tennessee, Niagara Falls, New York, and Becancour, Canada.
Other major US producers include Oxychem, Westlake, Shintek and Formosa.
All of these companies use the chloralkali process.

Historically, sodium hydroxide was produced by treating sodium carbonate with calcium hydroxide in a metathesis reaction which takes advantage of the fact that sodium hydroxide is soluble, while calcium carbonate is not.
This process was called causticizing.

Ca(OH)2(aq) + Na2CO3(s) → CaCO3(s) + 2 NaOH(aq)
This process was superseded by the Solvay process in the late 19th century, which was in turn supplanted by the chloralkali process which is in use today.

Sodium hydroxide is also produced by combining pure sodium metal with water. The byproducts are hydrogen gas and heat, often resulting in a flame.

2 Na + 2 H2O → 2 NaOH + H2
This reaction is commonly used for demonstrating the reactivity of alkali metals in academic environments; however, it is not commercially viable, as the isolation of sodium metal is typically performed by reduction or electrolysis of sodium compounds including sodium hydroxide.

Uses
Sodium hydroxide is a popular strong base used in industry.
Sodium hydroxide is used in the manufacture of sodium salts and detergents, pH regulation, and organic synthesis.
In bulk, it is most often handled as an aqueous solution, since solutions are cheaper and easier to handle.

Sodium hydroxide is used in many scenarios where it is desirable to increase the alkalinity of a mixture, or to neutralize acids.

For example, in the petroleum industry, sodium hydroxide is used as an additive in drilling mud to increase alkalinity in bentonite mud systems, to increase the mud viscosity, and to neutralize any acid gas (such as hydrogen sulfide and carbon dioxide) which may be encountered in the geological formation as drilling progresses.

Another use is in Salt spray testing where pH needs to be regulated. Sodium hydroxide is used with hydrochloric acid to balance pH. The resultant salt, NaCl, is the corrosive agent used in the standard neutral pH salt spray test.

Poor quality crude oil can be treated with sodium hydroxide to remove sulfurous impurities in a process known as caustic washing.
As above, sodium hydroxide reacts with weak acids such as hydrogen sulfide and mercaptans to yield non-volatile sodium salts, which can be removed.

The waste which is formed is toxic and difficult to deal with, and the process is banned in many countries because of this.
In 2006, Trafigura used the process and then dumped the waste in Ivory Coast.

Other common uses of sodium hydroxide include:

For making soaps and detergents.
Sodium hydroxide is used for hard bar soap while potassium hydroxide is used for liquid soaps.
Sodium hydroxide is used more often than potassium hydroxide because it is cheaper and a smaller quantity is needed.

As drain cleaners that contain sodium hydroxide convert fats and grease that can clog pipes into soap, which dissolves in water. (see cleaning agent)

For making artificial textile fibres (such as Rayon).

In the manufacture of paper. Around 56% of sodium hydroxide produced is used by industry, 25% of which is used in the paper industry. (see chemical pulping)

In purifying bauxite ore from which aluminium metal is extracted. This is known as Bayer process. (see dissolving amphoteric metals and compounds)

In de-greasing metals, oil refining, and making dyes and bleaches.

In water treatment plants for pH regulation.
to treat bagels and pretzel dough, giving the distinctive shiny finish.

Chemical pulping
Main article: Pulp (paper)
Sodium hydroxide is also widely used in pulping of wood for making paper or regenerated fibers.
Along with sodium sulfide, sodium hydroxide is a key component of the white liquor solution used to separate lignin from cellulose fibers in the kraft process.

Sodium hydroxide also plays a key role in several later stages of the process of bleaching the brown pulp resulting from the pulping process.
These stages include oxygen delignification, oxidative extraction, and simple extraction, all of which require a strong alkaline environment with a pH > 10.5 at the end of the stages.

Tissue digestion
In a similar fashion, sodium hydroxide is used to digest tissues, as in a process that was used with farm animals at one time. This process involved placing a carcass into a sealed chamber, then adding a mixture of sodium hydroxide and water (which breaks the chemical bonds that keep the flesh intact).

This eventually turns the body into a liquid with coffee-like appearance, and the only solid that remains are bone hulls, which could be crushed between one's fingertips.

Sodium hydroxide is frequently used in the process of decomposing roadkill dumped in landfills by animal disposal contractors.
Due to its availability and low cost, it has been used by criminals to dispose of corpses.
Sodium hydroxidealian serial killer Leonarda Cianciulli used this chemical to turn dead bodies into soap.
In Mexico, a man who worked for drug cartels admitted disposing of over 300 bodies with it.

Sodium hydroxide is a dangerous chemical due to its ability to hydrolyze protein.
If a dilute solution is spilled on the skin, burns may result if the area is not washed thoroughly and for several minutes with running water.
Splashes in the eye can be more serious and can lead to blindness.

Dissolving amphoteric metals and compounds
Strong bases attack aluminium. Sodium hydroxide reacts with aluminium and water to release hydrogen gas.
The aluminium takes the oxygen atom from sodium hydroxide, which in turn takes the oxygen atom from the water, and releases the two hydrogen atoms.
The reaction thus produces hydrogen gas and sodium aluminate.
In this reaction, sodium hydroxide acts as an agent to make the solution alkaline, which aluminium can dissolve in.

2 Al + 2 NaOH + 2 H2O → 2 NaAlO2 + 3 H2
Sodium aluminate is an inorganic chemical that is used as an effective source of aluminium hydroxide for many industrial and technical applications.
Pure sodium aluminate (anhydrous) is a white crystalline solid having a formula variously given as NaAlO2, Na3AlO3, NaAl(OH)4, Na2O·Al2O3 or Na2Al2O4.
Formation of sodium tetrahydroxoaluminate(III) or hydrated sodium aluminate is given by:[38]

2 Al + 2 NaOH + 6 H2O → 2 NaAl(OH)4 + 3 H2
This reaction can be useful in etching, removing anodizing, or converting a polished surface to a satin-like finish, but without further passivation such as anodizing or alodining the surface may become degraded, either under normal use or in severe atmospheric conditions.

In the Bayer process, sodium hydroxide is used in the refining of alumina containing ores (bauxite) to produce alumina (aluminium oxide) which is the raw material used to produce aluminium metal via the electrolytic Hall-Héroult process.
Since the alumina is amphoteric, it dissolves in the sodium hydroxide, leaving impurities less soluble at high pH such as iron oxides behind in the form of a highly alkaline red mud.

Other amphoteric metals are zinc and lead which dissolve in concentrated sodium hydroxide solutions to give sodium zincate and sodium plumbate respectively.

Esterification and transesterification reagent
Sodium hydroxide is traditionally used in soap making (cold process soap, saponification).
Sodium hydroxide was made in the nineteenth century for a hard surface rather than liquid product because it was easier to store and transport.

For the manufacture of biodiesel, sodium hydroxide is used as a catalyst for the transesterification of methanol and triglycerides.
This only works with anhydrous sodium hydroxide, because combined with water the fat would turn into soap, which would be tainted with methanol.
NaOH is used more often than potassium hydroxide because it is cheaper and a smaller quantity is needed.
Due to production costs, NaOH, which is produced using common salt is cheaper than potassium hydroxide.

Food preparation
Food uses of sodium hydroxide include washing or chemical peeling of fruits and vegetables, chocolate and cocoa processing, caramel coloring production, poultry scalding, soft drink processing, and thickening ice cream.

Olives are often soaked in sodium hydroxide for softening; Pretzels and German lye rolls are glazed with a sodium hydroxide solution before baking to make them crisp.
Owing to the difficulty in obtaining food grade sodium hydroxide in small quantities for home use, sodium carbonate is often used in place of sodium hydroxide.
Sodium hydroxide is known as E number E524.

Specific foods processed with sodium hydroxide include:

German pretzels are poached in a boiling sodium carbonate solution or cold sodium hydroxide solution before baking, which contributes to their unique crust.
Lye-water is an essential ingredient in the crust of the traditional baked Chinese moon cakes.
Most yellow coloured Chinese noodles are made with lye-water but are commonly mistaken for containing egg.
One variety of zongzi uses lye water to impart a sweet flavor.

Sodium hydroxide is also the chemical that causes gelling of egg whites in the production of Century eggs.
Some methods of preparing olives involve subjecting them to a lye-based brine.
The Filipino dessert (kakanin) called kutsinta uses a small quantity of lye water to help give the rice flour batter a jelly like consistency. A similar process is also used in the kakanin known as pitsi-pitsi or pichi-pichi except that the mixture uses grated cassava instead of rice flour.

The Norwegian dish known as lutefisk (from lutfisk, "lye fish").
Bagels are often boiled in a lye solution before baking, contributing to their shiny crust.
Hominy is dried maize (corn) kernels reconstituted by soaking in lye-water.
These expand considerably in size and may be further processed by frying to make corn nuts or by drying and grinding to make grits.

Hominy is used to create Masa, a popular flour used in Mexican cuisine to make Corn tortillas and tamales. Nixtamal is similar, but uses calcium hydroxide instead of sodium hydroxide.

Cleaning agent
Main article: Cleaning agent
Sodium hydroxide is frequently used as an industrial cleaning agent where it is often called "caustic".
Sodium hydroxide is added to water, heated, and then used to clean process equipment, storage tanks, etc. Sodium hydroxide can dissolve grease, oils, fats and protein-based deposits.

Sodium hydroxide is also used for cleaning waste discharge pipes under sinks and drains in domestic properties.
Surfactants can be added to the sodium hydroxide solution in order to stabilize dissolved substances and thus prevent redeposition.
A sodium hydroxide soak solution is used as a powerful degreaser on stainless steel and glass bakeware.
Sodium hydroxide is also a common ingredient in oven cleaners.

A common use of sodium hydroxide is in the production of parts washer detergents.
Parts washer detergents based on sodium hydroxide are some of the most aggressive parts washer cleaning chemicals.
The sodium hydroxide-based detergents include surfactants, rust inhibitors and defoamers.
A parts washer heats water and the detergent in a closed cabinet and then sprays the heated sodium hydroxide and hot water at pressure against dirty parts for degreasing applications.

Sodium hydroxide used in this manner replaced many solvent-based systems in the early 1990s[citation needed] when trichloroethane was outlawed by the Montreal Protocol. Water and sodium hydroxide detergent-based parts washers are considered to be an environmental improvement over the solvent-based cleaning methods.

Storage
Careful storage is needed when handling sodium hydroxide for use, especially bulk volumes.
Following proper NaOH storage guidelines and maintaining worker/environment safety is always recommended given the chemical's burn hazard.

Sodium hydroxide is often stored in bottles for small-scale laboratory use, within intermediate bulk containers (medium volume containers) for cargo handling and transport, or within large stationary storage tanks with volumes up to 100,000 gallons for manufacturing or waste water plants with extensive NaOH use.

Common materials that are compatible with sodium hydroxide and often utilized for NaOH storage include: polyethylene (HDPE, usual, XLPE, less common), carbon steel, polyvinyl chloride (PVC), stainless steel, and fiberglass reinforced plastic (FRP, with a resistant liner).

Sodium hydroxide must be stored in airtight containers to preserve its normality as it will absorb water from the atmosphere.

History
Sodium hydroxide was first prepared by soap makers.
A procedure for making sodium hydroxide appeared as part of a recipe for making soap in an Arab book of the late 13th century: Al-mukhtara' fi funun min al-suna' (Inventions from the Various Industrial Arts), which was compiled by al-Muzaffar Yusuf ibn 'Umar ibn 'Ali ibn Rasul (d. 1295), a king of Yemen.

The recipe called for passing water repeatedly through a mixture of alkali (Arabic: al-qily, where qily is ash from saltwort plants, which are rich in sodium; hence alkali was impure sodium carbonate) and quicklime (calcium oxide, CaO), whereby a solution of sodium hydroxide was obtained. European soap makers also followed this recipe.

When in 1791 the French chemist and surgeon Nicolas Leblanc (1742–1806) patented a process for mass-producing sodium carbonate, natural "soda ash" (impure sodium carbonate that was obtained from the ashes of plants that are rich in sodium): was replaced by this artificial version.
However, by the 20th century, the electrolysis of sodium chloride had become the primary method for producing sodium hydroxide.

Appearance: White, hard (when pure), opaque crystals
Odor: odorless
Density: 2.13 g/cm3
Melting point: 323 °C
Boiling point: 1,388 °C
Solubility in water: 418 g/L (0 °C) - 1000 g/L (25 °C) - 3370 g/L (100 °C)
Solubility: soluble in glycerol - negligible in ammonia - insoluble in ether - slowly soluble in propylene glycol
Solubility in methanol: 238 g/L
Solubility in ethanol: <<139 g/L
Vapor pressure: <2.4 kPa (at 20 °C)
Acidity (pKa): 15.7
Magnetic susceptibility (χ): −15.8·10−6 cm3/mol (aq.)[5]
Refractive index (nD): 1.3576
Crystal structure: Orthorhombic, oS8
Space group: Cmcm, No. 63
Lattice constant: a = 0.34013 nm, b = 1.1378 nm, c = 0.33984 nm
Formula units (Z): 4
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 0
Exact Mass: 39.99250893
Monoisotopic Mass: 39.99250893
Topological Polar Surface Area: 1 Ų
Heavy Atom Count: 2
Complexity: 2
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 2
Compound Is Canonicalized: Yes

Thermochemistry
Heat capacity (C): 59.5 J/mol K
Std molar entropy (So298): 64.4 J·mol−1·K−1
Std enthalpy of formation (ΔfH⦵298): −425.8 kJ·mol−1
Gibbs free energy (ΔfG˚): -379.7 kJ/mol

About Sodium hydroxide
Sodium hydroxide is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 000 tonnes per annum.

Sodium hydroxide is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.

Consumer Uses
Other release to the environment of Sodium hydroxide is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters), outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids), indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment), outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials), indoor use in long-life materials with high release rate (e.g. release from fabrics, textiles during washing, removal of indoor paints) and outdoor use in long-life materials with high release rate (e.g. tyres, treated wooden products, treated textile and fabric, brake pads in trucks or cars, sanding of buildings (bridges, facades) or vehicles (ships)).

Article service life
Other release to the environment of Sodium hydroxide is likely to occur from: outdoor use, indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment) and indoor use in long-life materials with high release rate (e.g. release from fabrics, textiles during washing, removal of indoor paints).

Sodium hydroxide can be found in products with material based on: fabrics, textiles and apparel (e.g. clothing, mattress, curtains or carpets, textile toys), leather (e.g. gloves, shoes, purses, furniture), metal (e.g. cutlery, pots, toys, jewellery) and stone, plaster, cement, glass or ceramic (e.g. dishes, pots/pans, food storage containers, construction and isolation material).

Widespread uses by professional workers
Sodium hydroxide is used in the following areas: mining.
Sodium hydroxide is used for the manufacture of: chemicals.
Release to the environment of Sodium hydroxide can occur from industrial use: formulation of mixtures and formulation in materials.
Other release to the environment of Sodium hydroxide is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters), outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids), outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials), indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment), outdoor use in long-life materials with high release rate (e.g. tyres, treated wooden products, treated textile and fabric, brake pads in trucks or cars, sanding of buildings (bridges, facades) or vehicles (ships)) and indoor use in long-life materials with high release rate (e.g. release from fabrics, textiles during washing, removal of indoor paints).

Formulation or re-packing
ECHA has no public registered data indicating whether or in which chemical products the substance might be used.
Release to the environment of Sodium hydroxide can occur from industrial use: formulation of mixtures, formulation in materials, as processing aid, as processing aid, in pro
SODIUM HYDROXIDE LIQUID
Sodium Hydroxide Liquid Sodium hydroxide liquid, also known as lye and caustic soda, is an inorganic compound with the formula NaOH. It is a white solid ionic compound consisting of sodium cations Na+ and hydroxide anions OH−. Sodium hydroxide liquid is a highly caustic base and alkali that decomposes proteins at ordinary ambient temperatures and may cause severe chemical burns. It is highly soluble in water, and readily absorbs moisture and carbon dioxide from the air. It forms a series of hydrates NaOH·nH2O. The monohydrate NaOH·H2O crystallizes from water solutions between 12.3 and 61.8 °C. The commercially available "Sodium hydroxide liquid" is often this monohydrate, and published data may refer to it instead of the anhydrous compound. As one of the simplest hydroxides, Sodium hydroxide liquid is frequently utilized alongside neutral water and acidic hydrochloric acid to demonstrate the pH scale to chemistry students. Sodium hydroxide liquid is used in many industries: in the manufacture of pulp and paper, textiles, drinking water, soaps and detergents, and as a drain cleaner. Worldwide production in 2004 was approximately 60 million tonnes, while demand was 51 million tonnes. Properties of Sodium hydroxide liquid Chemical formula NaOH Molar mass 39.9971 g mol−1 Appearance White, waxy, opaque crystals Odor odorless Density 2.13 g/cm3 Melting point 323 °C (613 °F; 596 K) Boiling point 1,388 °C (2,530 °F; 1,661 K) Solubility in water 418 g/L (0 °C) 1000 g/L (25 °C) 3370 g/L (100 °C) Solubility soluble in glycerol negligible in ammonia insoluble in ether slowly soluble in propylene glycol Solubility in methanol 238 g/L Solubility in ethanol <<139 g/L Vapor pressure <2.4 kPa (at 20 °C) Basicity (pKb) 0.2 Magnetic susceptibility (χ) −15.8·10−6 cm3/mol (aq.) Refractive index (nD) 1.3576 Properties of Sodium hydroxide liquid Physical properties Sodium hydroxide liquid Pure Sodium hydroxide liquid is a colorless crystalline solid that melts at 318 °C (604 °F) without decomposition, and with a boiling point of 1,388 °C (2,530 °F). It is highly soluble in water, with a lower solubility in polar solvents such as ethanol and methanol. NaOH is insoluble in ether and other non-polar solvents. Similar to the hydration of sulfuric acid, dissolution of solid Sodium hydroxide liquid in water is a highly exothermic reaction where a large amount of heat is liberated, posing a threat to safety through the possibility of splashing. The resulting solution is usually colorless and odorless. As with other alkaline solutions, it feels slippery with skin contact due to the process of saponification that occurs between NaOH and natural skin oils. Viscosity of Sodium hydroxide liquid Concentrated (50%) aqueous solutions of Sodium hydroxide liquid have a characteristic viscosity, 78 mPa·s, that is much greater than that of water (1.0 mPa·s) and near that of olive oil (85 mPa·s) at room temperature. The viscosity of aqueous NaOH, as with any liquid chemical, is inversely related to its service temperature, i.e., its viscosity decreases as temperature increases, and vice versa. The viscosity of Sodium hydroxide liquid solutions plays a direct role in its application as well as its storage. Hydrates Sodium hydroxide liquid can form several hydrates NaOH·nH2O, which result in a complex solubility diagram that was described in detail by S. U. Pickering in 1893. The known hydrates and the approximate ranges of temperature and concentration (mass percent of NaOH) of their saturated water solutions are: Heptahydrate, NaOH·7H2O: from −28 °C (18.8%) to −24 °C (22.2%). Pentahydrate, NaOH·5H2O: from −24 °C (22.2%) to −17.7 (24.8%). Tetrahydrate, NaOH·4H2O, α form: from −17.7 (24.8%) to +5.4 °C (32.5%). Tetrahydrate, NaOH·4H2O, β form: metastable. Trihemihydrate, NaOH·3.5H2O: from +5.4 °C (32.5%) to +15.38 °C (38.8%) and then to +5.0 °C (45.7%). Trihydrate, NaOH·3H2O: metastable. Dihydrate, NaOH·2H2O: from +5.0 °C (45.7%) to +12.3 °C (51%). Monohydrate, NaOH·H2O: from +12.3 °C (51%) to 65.10 °C (69%) then to 62.63 °C (73.1%). Early reports refer to hydrates with n = 0.5 or n = 2/3, but later careful investigations failed to confirm their existence. The only hydrates with stable melting points are NaOH·H2O (65.10 °C) and NaOH·3.5H2O (15.38 °C). The other hydrates, except the metastable ones NaOH·3H2O and NaOH·4H2O (β) can be crystallized from solutions of the proper composition, as listed above. However, solutions of NaOH can be easily supercooled by many degrees, which allows the formation of hydrates (including the metastable ones) from solutions with different concentrations. For example, when a solution of Sodium hydroxide liquid and water with 1:2 mole ratio (52.6% Sodium hydroxide liquid by mass) is cooled, the monohydrate normally starts to crystallize (at about 22 °C) before the dihydrate. However, the solution can easily be supercooled down to −15 °C, at which point it may quickly crystallize as the dihydrate. When heated, the solid dihydrate might melt directly into a solution at 13.35 °C; however, once the temperature exceeds 12.58 °C. it often decomposes into solid monohydrate and a liquid solution. Even the n = 3.5 hydrate is difficult to crystallize, because the solution supercools so much that other hydrates become more stable. A hot water solution containing 73.1% (mass) of Sodium hydroxide liquid is an eutectic that solidifies at about 62.63 °C as an intimate mix of anhydrous and monohydrate crystals. A second stable eutectic composition is 45.4% (mass) of Sodium hydroxide liquid, that solidifies at about 4.9 °C into a mixture of crystals of the dihydrate and of the 3.5-hydrate. The third stable eutectic has 18.4% (mass) of Sodium hydroxide liquid. It solidifies at about −28.7 °C as a mixture of water ice and the heptahydrate Sodium hydroxide liquid·7H2O. When solutions with less than 18.4% Sodium hydroxide liquid are cooled, water ice crystallizes first, leaving the Sodium hydroxide liquid in solution. The α form of the tetrahydrate has density 1.33 g/cm3. It melts congruously at 7.55 °C into a liquid with 35.7% Sodium hydroxide liquid and density 1.392 g/cm3, and therefore floats on it like ice on water. However, at about 4.9 °C it may instead melt incongruously into a mixture of solid Sodium hydroxide liquid·3.5H2O and a liquid solution. The β form of the tetrahydrate is metastable, and often transforms spontaneously to the α form when cooled below −20 °C. Once initiated, the exothermic transformation is complete in a few minutes, with a 6.5% increase in volume of the solid. The β form can be crystallized from supercooled solutions at −26 °C, and melts partially at −1.83 °C. The "sodium hydroxide" of commerce is often the monohydrate (density 1.829 g/cm3). Physical data in technical literature may refer to this form, rather than the anhydrous compound. Crystal structure of Sodium hydroxide liquid Sodium hydroxide liquid and its monohydrate form orthorhombic crystals with the space groups Cmcm (oS8) and Pbca (oP24), respectively. The monohydrate cell dimensions are a = 1.1825, b = 0.6213, c = 0.6069 nm. The atoms are arranged in a hydrargillite-like layer structure /O Na OO NaO/... Each sodium atom is surrounded by six oxygen atoms, three each from hydroxyl anions HO− and three from water molecules. The hydrogen atoms of the hydroxyls form strong bonds with oxygen atoms within each O layer. Adjacent O layers are held together by hydrogen bonds between water molecules. Chemical properties of Sodium hydroxide liquid Reaction with acids of Sodium hydroxide liquid Sodium hydroxide liquid reacts with protic acids to produce water and the corresponding salts. For example, when Sodium hydroxide liquid reacts with hydrochloric acid, sodium chloride is formed: NaOH(aq) + HCl(aq) → NaCl(aq) +H2O(l) In general, such neutralization reactions are represented by one simple net ionic equation: OH−(aq) + H+(aq) → H2O(l) This type of reaction with a strong acid releases heat, and hence is exothermic. Such acid-base reactions can also be used for titrations. However, Sodium hydroxide liquid is not used as a primary standard because it is hygroscopic and absorbs carbon dioxide from air. Reaction with acidic oxides Sodium hydroxide liquid also reacts with acidic oxides, such as sulfur dioxide. Such reactions are often used to "scrub" harmful acidic gases (like SO2 and H2S) produced in the burning of coal and thus prevent their release into the atmosphere. For example, 2 NaOH + SO2 → Na2SO3 + H2O Reaction with metals and oxides Glass reacts slowly with aqueous Sodium hydroxide liquid solutions at ambient temperatures to form soluble silicates. Because of this, glass joints and stopcocks exposed to Sodium hydroxide liquid have a tendency to "freeze". Flasks and glass-lined chemical reactors are damaged by long exposure to hot Sodium hydroxide liquid, which also frosts the glass. Sodium hydroxide liquid does not attack iron at room temperatures, since iron does not have amphoteric properties (i.e., it only dissolves in acid, not base). Nevertheless, at high temperatures (e.g. above 500 °C), iron can react endothermically with Sodium hydroxide liquid to form iron(III) oxide, sodium metal, and hydrogen gas. This is due to the lower enthalpy of formation of iron(III) oxide (−824.2 kJ/mol compared to Sodium hydroxide liquid (-500 kJ/mol), thus the reaction is thermodynamically favorable, although its endothermic nature indicates non-spontaneity. Consider the following reaction between molten Sodium hydroxide liquid and finely divided iron filings: 4 Fe + 6 NaOH → 2 Fe2O3 + 6 Na + 3 H2 A few transition metals, however, may react vigorously with Sodium hydroxide liquid. In 1986, an aluminium road tanker in the UK was mistakenly used to transport 25% Sodium hydroxide liquid solution, causing pressurization of the contents and damage to the tanker. The pressurization was due to the hydrogen gas which is produced in the reaction between Sodium hydroxide liquid and aluminium: 2 Al + 2 NaOH + 6 H2O → 2 NaAl(OH)4 + 3 H2 Precipitant Unlike Sodium hydroxide liquid, which is soluble, the hydroxides of most transition metals are insoluble, and therefore Sodium hydroxide liquid can be used to precipitate transition metal hydroxides. The following colours are observed: Copper - blue Iron(II) - green Iron(III) - yellow / brown Zinc and lead salts dissolve in excess Sodium hydroxide liquid to give a clear solution of Na2ZnO2 or Na2PbO2. Aluminium hydroxide is used as a gelatinous flocculant to filter out particulate matter in water treatment. Aluminium hydroxide is prepared at the treatment plant from aluminium sulfate by reacting it with Sodium hydroxide liquid or bicarbonate. Al2(SO4)3 + 6 NaOH → 2 Al(OH)3 + 3 Na2SO4Al2(SO4)3 + 6 NaHCO3 → 2 Al(OH)3 + 3 Na2SO4 + 6 CO2 Saponification Sodium hydroxide liquid can be used for the base-driven hydrolysis of esters (as in saponification), amides and alkyl halides. However, the limited solubility of Sodium hydroxide liquid in organic solvents means that the more soluble potassium hydroxide (KOH) is often preferred. Touching Sodium hydroxide liquid solution with the bare hands, while not recommended, produces a slippery feeling. This happens because oils on the skin such as sebum are converted to soap. Despite solubility in propylene glycol it is unlikely to replace water in saponification due to propylene glycol primary reaction with fat before reaction between Sodium hydroxide liquid and fat. Production For historical information, see Alkali manufacture. Sodium hydroxide liquid is industrially produced as a 50% solution by variations of the electrolytic chloralkali process. Chlorine gas is also produced in this process. Solid Sodium hydroxide liquid is obtained from this solution by the evaporation of water. Solid Sodium hydroxide liquid is most commonly sold as flakes, prills, and cast blocks. In 2004, world production was estimated at 60 million dry tonnes of Sodium hydroxide liquid, and demand was estimated at 51 million tonnes. In 1998, total world production was around 45 million tonnes. North America and Asia each contributed around 14 million tonnes, while Europe produced around 10 million tonnes. In the United States, the major producer of Sodium hydroxide liquid is the Dow Chemical Company, which has annual production around 3.7 million tonnes from sites at Freeport, Texas, and Plaquemine, Louisiana. Other major US producers include Oxychem, Westlake, Olin, Shintek and Formosa. All of these companies use the chloralkali process. Historically, Sodium hydroxide liquid was produced by treating sodium carbonate with calcium hydroxide in a metathesis reaction which takes advantage of the fact that Sodium hydroxide liquid is soluble, while calcium carbonate is not. This process was called causticizing. Ca(OH)2(aq) + Na2CO3(s) → CaCO3(s) + 2 NaOH(aq) This process was superseded by the Solvay process in the late 19th century, which was in turn supplanted by the chloralkali process which we use today. Sodium hydroxide liquid is also produced by combining pure sodium metal with water. The byproducts are hydrogen gas and heat, often resulting in a flame. 2 Na + 2 H2O → 2 NaOH + H2 This reaction is commonly used for demonstrating the reactivity of alkali metals in academic environments; however, it is not commercially viable, as the isolation of sodium metal is typically performed by reduction or electrolysis of sodium compounds including Sodium hydroxide liquid. Uses Sodium hydroxide liquid is a popular strong base used in industry. Sodium hydroxide liquid is used in the manufacture of sodium salts and detergents, pH regulation, and organic synthesis. In bulk, it is most often handled as an aqueous solution, since solutions are cheaper and easier to handle. Sodium hydroxide liquid is used in many scenarios where it is desirable to increase the alkalinity of a mixture, or to neutralize acids. For example, in the petroleum industry, Sodium hydroxide liquid is used as an additive in drilling mud to increase alkalinity in bentonite mud systems, to increase the mud viscosity, and to neutralize any acid gas (such as hydrogen sulfide and carbon dioxide) which may be encountered in the geological formation as drilling progresses. Another use is in Salt spray testing where pH needs to be regulated. Sodium hydroxide liquid is used with hydrochloric acid to balance pH. The resultant salt, NaCl, is the corrosive agent used in the standard neutral pH salt spray test. Poor quality crude oil can be treated with Sodium hydroxide liquid to remove sulfurous impurities in a process known as caustic washing. As above, Sodium hydroxide liquid reacts with weak acids such as hydrogen sulfide and mercaptans to yield non-volatile sodium salts, which can be removed. The waste which is formed is toxic and difficult to deal with, and the process is banned in many countries because of this. In 2006, Trafigura used the process and then dumped the waste in Ivory Coast. Other common uses of Sodium hydroxide liquid include: It is used for making soaps and detergents. Sodium hydroxide liquid is used for hard bar soap while potassium hydroxide is used for liquid soaps.Sodium hydroxide liquid is used more often than potassium hydroxide because it is cheaper and a smaller quantity is needed. It is used as drain cleaners that contain Sodium hydroxide liquid convert fats and grease that can clog pipes into soap, which dissolves in water. (see cleaning agent) It is used for making artificial textile fibres (such as Rayon). It is used in the manufacture of paper. Around 56% of Sodium hydroxide liquid produced is used by industry, 25% of which is used in the paper industry. (see chemical pulping) It is used in purifying bauxite ore from which aluminium metal is extracted. This is known as Bayer process. (see dissolving amphoteric metals and compounds) It is used in de-greasing metals, oil refining, and making dyes and bleaches. Chemical pulping Sodium hydroxide liquid is also widely used in pulping of wood for making paper or regenerated fibers. Along with sodium sulfide, Sodium hydroxide liquid is a key component of the white liquor solution used to separate lignin from cellulose fibers in the kraft process. It also plays a key role in several later stages of the process of bleaching the brown pulp resulting from the pulping process. These stages include oxygen delignification, oxidative extraction, and simple extraction, all of which require a strong alkaline environment with a pH > 10.5 at the end of the stages. Tissue digestion In a similar fashion, Sodium hydroxide liquid is used to digest tissues, as in a process that was used with farm animals at one time. This process involved placing a carcass into a sealed chamber, then adding a mixture of Sodium hydroxide liquid and water (which breaks the chemical bonds that keep the flesh intact). This eventually turns the body into a liquid with coffee-like appearance, and the only solid that remains are bone hulls, which could be crushed between one's fingertips. Sodium hydroxide liquid is frequently used in the process of decomposing roadkill dumped in landfills by animal disposal contractors. Due to its availability and low cost, it has been used by criminals to dispose of corpses. Italian serial killer Leonarda Cianciulli used this chemical to turn dead bodies into soap. In Mexico, a man who worked for drug cartels admitted disposing of over 300 bodies with it. Sodium hydroxide liquid is a dangerous chemical due to its ability to hydrolyze protein. If a dilute solution is spilled on the skin, burns may result if the area is not washed thoroughly and for several minutes with running water. Splashes in the eye can be more serious and can lead to blindness. Dissolving amphoteric metals and compounds Strong bases attack aluminium. Sodium hydroxide liquid reacts with aluminium and water to release hydrogen gas. The aluminium takes the oxygen atom from Sodium hydroxide liquid, which in turn takes the oxygen atom from the water, and releases the two hydrogen atoms, The reaction thus produces hydrogen gas and sodium aluminate. In this reaction, Sodium hydroxide liquid acts as an agent to make the solution alkaline, which aluminium can dissolve in. 2 Al + 2 NaOH + 2 H2O → 2 NaAlO2 + 3H2 Sodium aluminate is an inorganic chemical that is used as an effective source of aluminium hydroxide for many industrial and technical applications. Pure sodium aluminate (anhydrous) is a white crystalline solid having a formula variously given as NaAlO2, NaAl(OH)4< (hydrated), Na2O.Al2O3, or Na2Al2O4. Formation of sodium tetrahydroxoaluminate(III) or hydrated sodium aluminate is given by: 2Al + 2NaOH + 6H2O → 2 NaAl(OH)4 + 3 H2 This reaction can be useful in etching, removing anodizing, or converting a polished surface to a satin-like finish, but without further passivation such as anodizing or alodining the surface may become degraded, either under normal use or in severe atmospheric conditions. In the Bayer process, Sodium hydroxide liquid is used in the refining of alumina containing ores (bauxite) to produce alumina (aluminium oxide) which is the raw material used to produce aluminium metal via the electrolytic Hall-Héroult process. Since the alumina is amphoteric, it dissolves in the Sodium hydroxide liquid, leaving impurities less soluble at high pH such as iron oxides behind in the form of a highly alkaline red mud. Other amphoteric metals are zinc and lead which dissolve in concentrated Sodium hydroxide liquid solutions to give sodium zincate and sodium plumbate respectively. Esterification and transesterification reagent Sodium hydroxide liquid is traditionally used in soap making (cold process soap, saponification). It was made in the nineteenth century for a hard surface rather than liquid product because it was easier to store and transport. For the manufacture of biodiesel, Sodium hydroxide liquid is used as a catalyst for the transesterification of methanol and triglycerides. This only works with anhydrous Sodium hydroxide liquid, because combined with water the fat would turn into soap, which would be tainted with methanol. NaOH is used more often than potassium hydroxide because it is cheaper and a smaller quantity is needed. Due to production costs, NaOH, which is produced using common salt is cheaper than potassium hydroxide. Food preparation Food uses of Sodium hydroxide liquid include washing or chemical peeling of fruits and vegetables, chocolate and cocoa processing, caramel coloring production, poultry scalding, soft drink processing, and thickening ice cream. Olives are often soaked in Sodium hydroxide liquid for softening; Pretzels and German lye rolls are glazed with a Sodium hydroxide liquid solution before baking to make them crisp. Owing to the difficulty in obtaining food grade Sodium hydroxide liquid in small quantities for home use, sodium carbonate is often used in place of Sodium hydroxide liquid. It is known as E number E524. Specific foods processed with Sodium hydroxide liquid include: German pretzels are poached in a boiling sodium carbonate solution or cold Sodium hydroxide liquid solution before baking, which contributes to their unique crust. Lye-water is an essential ingredient in the crust of the traditional baked Chinese moon cakes. Most yellow coloured Chinese noodles are made with lye-water but are commonly mistaken for containing egg. One variety of zongzi uses lye water to impart a sweet flavor. Sodium hydroxide liquid is also the chemical that causes gelling of egg whites in the production of Century eggs. Some methods of preparing olives involve subjecting them to a lye-based brine. The Filipino dessert (kakanin) called kutsinta uses a small quantity of lye water to help give the rice flour batter a jelly like consistency. A similar process is also used in the kakanin known as pitsi-pitsi or pichi-pichi except that the mixture uses grated cassava instead of rice flour. The Norwegian dish known as lutefisk (from lutfisk, "lye fish"). Bagels are often boiled in a lye solution before baking, contributing to their shiny crust. Hominy is dried maize (corn) kernels reconstituted by soaking in lye-water. These expand considerably in size and may be further processed by frying to make corn nuts or by drying and grinding to make grits. Hominy is used to create Masa, a popular flour used in Mexican cuisine to make Corn tortillas and tamales. Nixtamal is similar, but uses calcium hydroxide instead of Sodium hydroxide liquid. Cleaning agent Sodium hydroxide liquid is frequently used as an industrial cleaning agent where it is often called "caustic". It is added to water, heated, and then used to clean process equipment, storage tanks, etc. It can dissolve grease, oils, fats and protein-based deposits. It is also used for cleaning waste discharge pipes under sinks and drains in domestic properties. Surfactants can be added to the Sodium hydroxide liquid solution in order to stabilize dissolved substances and thus prevent redeposition. A Sodium hydroxide liquid soak solution is used as a powerful degreaser on stainless steel and glass bakeware. It is also a common ingredient in oven cleaners. A common use of Sodium hydroxide liquid is in the production of parts washer detergents. Parts washer detergents based on Sodium hydroxide liquid are some of the most aggressive parts washer cleaning chemicals. The Sodium hydroxide liquid-based detergents include surfactants, rust inhibitors and defoamers. A parts washer heats water and the detergent in a closed cabinet and then sprays the heated Sodium hydroxide liquid and hot water at pressure against dirty parts for degreasing applications. Sodium hydroxide liquid used in this manner replaced many solvent-based systems in the early 1990s when trichloroethane was outlawed by the Montreal Protocol. Water and Sodium hydroxide liquid detergent-based parts washers are considered to be an environmental improvement over the solvent-based cleaning methods. Hardware stores grade Sodium hydroxide liquid to be used as a type of drain cleaner. Paint stripping with caustic soda Sodium hydroxide liquid is used in the home as a type of drain opener to unblock clogged drains, usually in the form of a dry crystal or as a thick liquid gel. The alkali dissolves greases to produce water soluble products. It also hydrolyzes the proteins such as those found in hair which may block water pipes. These reactions are sped by the heat generated when Sodium hydroxide liquid and the other chemical components of the cleaner dissolve in water. Such alkaline drain cleaners and their acidic versions are highly corrosive and should be handled with great caution. Sodium hydroxide liquid is used in some relaxers to straighten hair. However, because of the high incidence and intensity of chemical burns, manufacturers of chemical relaxers use other alkaline chemicals in preparations available to average consumers. Sodium hydroxide liquid relaxers are still available, but they are used mostly by professionals. A solution of Sodium hydroxide liquid in water was traditionally used as the most common paint stripper on wooden objects. Its use has become less common, because it can damage the wood surface, raising the grain and staining the colour. Water treatment of Sodium hydroxide liquid Sodium hydroxide liquid is sometimes used during water purification to raise the pH of water supplies. Increased pH makes the water less corrosive to plumbing and reduces the amount of lead, copper and other toxic metals that can dissolve into drinking water. Historical uses of Sodium hydroxide liquid Sodium hydroxide liquid has been used for detection of carbon monoxide poisoning, with blood samples of such patients turning to a vermilion color upon the addition of a few drops of Sodium hydroxide liquid. Today, carbon monoxide poisoning can be detected by CO oximetry. In cement mixes, mortars, concrete, grouts Sodium hydroxide liquid is used in some cement mix plasticisers. This helps homogenise cement mixes, preventing segregation of sands and cement, decreases the amount of water required in a mix and increases workability of the cement product, be it mortar, render or concrete. Summer-winter heat storage EMPA researchers are experimenting with concentrated Sodium hydroxide liquid (NaOH) as the thermal storage or seasonal reservoir medium for domestic space-heating. If water is added to solid or concentrated Sodium hydroxide liquid (NaOH), heat is released. The dilution is exothermic – chemical energy is released in the form of heat. Conversely, by applying heat energy into a dilute Sodium hydroxide liquid solution the water will evaporate so that the solution becomes more concentrated and thus stores the supplied heat as latent chemical energy. Neutron Moderator Seaborg is working on a reactor design in which NaOH is used as a neutron moderator. Safety of Sodium hydroxide liquid Like other corrosive acids and alkalis, drops of Sodium hydroxide liquid solutions can readily decompose proteins and lipids in living tissues via amide hydrolysis and ester hydrolysis, which consequently cause chemical burns and may induce permanent blindness upon contact with eyes. Solid alkali can also express its corrosive nature if there is water, such as water vapor. Thus, protective equipment, like rubber gloves, safety clothing and eye protection, should always be used when handling this chemical or its solutions. The standard first aid measures for alkali spills on the skin is, as for other corrosives, irrigation with large quantities of water. Washing is continued for at least ten to fifteen minutes. Moreover, dissolution of Sodium hydroxide liquid is highly exothermic, and the resulting heat may cause heat burns or ignite flammables. It also produces heat when reacted with acids. Sodium hydroxide liquid is also mildly corrosive to glass, which can cause damage to glazing or cause ground glass joints to bind. Sodium hydroxide liquid is corrosive to several metals, like aluminium which reacts with the alkali to produce flammable hydrogen gas on contact: 2 Al + 6 NaOH → 3 H2 + 2 Na3AlO3 2 Al + 2 NaOH + 2 H2O → 3 H2 + 2 NaAlO2 2 Al + 2 NaOH + 6 H2O → 3 H2 + 2 NaAl(OH)4 Storage Careful storage is needed when handling Sodium hydroxide liquid for use, especially bulk volumes. Following proper NaOH storage guidelines and maintaining worker/environment safety is always recommended given the chemical's burn hazard. Sodium hydroxide liquid is often stored in bottles for small-scale laboratory use, within intermediate bulk containers (medium volume containers) for cargo handling and transport, or within large stationary storage tanks with volumes up to 100,000 gallons for manufacturing or waste water plants with extensive NaOH use. Common materials that are compatible with Sodium hydroxide liquid and often utilized for NaOH storage include: polyethylene (HDPE, usual, XLPE, less common), carbon steel, polyvinyl chloride (PVC), stainless steel, and fiberglass reinforced plastic (FRP, with a resistant liner). Sodium hydroxide liquid must be stored in airtight containers to preserve its normality as it will absorb water from the atmosphere. History of Sodium hydroxide liquid Sodium hydroxide liquid was first prepared by soap makers. A procedure for making Sodium hydroxide liquid appeared as part of a recipe for making soap in an Arab book of the late 13th century: Al-mukhtara` fi funun min al-suna` (Inventions from the Various Industrial Arts), which was compiled by al-Muzaffar Yusuf ibn `Umar ibn `Ali ibn Rasul (d. 1295), a king of Yemen. The recipe called for passing water repeatedly through a mixture of alkali (Arabic: al-qily, where qily is ash from saltwort plants, which are rich in sodium ; hence alkali was impure sodium carbonate) and quicklime (calcium oxide, CaO), whereby a solution of Sodium hydroxide liquid was obtained. European soap makers also followed this recipe. When in 1791 the French chemist and surgeon Nicolas Leblanc (1742–1806) patented a process for mass-producing sodium carbonate, natural "soda ash" (impure sodium carbonate that was obtained from the ashes of plants that are rich in sodium) was replaced by this artificial version. However, by the 20th century, the electrolysis of sodium chloride had become the primary method for producing Sodium hydroxide liquid. Sodium hydroxide liquid solution appears as a colorless liquid. More dense than water. Contact may severely irritate skin, eyes, and mucous membranes. Toxic by ingestion. Corrosive to metals and tissue. Caustic soda reacts with all the mineral acids to form the corresponding salts. It also reacts with weak-acid gases, such as hydrogen sulfide, sulfur dioxide, and carbon dioxide. Caustic soda reacts with amphoteric metals (Al, Zn, Sn) and their oxides to form complex anions such as AlO2(-), ZnO2(-2), SNO2(-2), and H2 (or H2O with oxides). All organic acids also react with sodium hydroxide liquid to form soluble salts. Another common reaction of caustic soda is dehydrochlorination. Because of its high-level alkalinity, sodium hydroxide in aqueous solution directly causes bond breakage in proteins (especially disulfide bridges). Hair and fingernails are found to be dissolved after 20 hours of direct contact with sodium hydroxide at pH values higher than 9.2. Sodium hydroxide has depilatory effects which have been described after accidental contact with solutions in the workplace. The breakage of bonds in proteins may lead to severe necrosis to the application site. The level of corrosion depends on the period of contact with the tissue, and on the concentration of sodium hydroxide. Liquid or solid sodium hydroxide is a severe skin irritant. It causes second and third degree burns on short contact and is very injurious to the eyes. The organic chemical industry uses Sodium hydroxide liquid for saponification reactions, production of nucleophilic anionic intermediates, etherification and esterification, basic catalysis, and the production of free organic bases. Sodium hydroxide liquid solution is used for scrubbingwaste gases and neutralizing wastewater. In inorganic chemistry, Sodium hydroxide liquid is used in the manufacture of sodium salts, for alkaline ore digestion, and for pH regulation.
SODIUM HYDROXYMETHANE SULFONATE
SYNONYMS Sodium chloride oxide; Sodium oxychloride; Hypochlorite sodium; Bleach Liquor; active chlorine; Hychlorite; Hipofosfito De Sodio; Hypochlorous acid sodium salt; CAS NO. 7681-52-9
SODIUM HYPOCHLORITE
Sodium Hypochlorite Sodium hypochlorite is most often encountered as a pale greenish-yellow dilute solution referred to as liquid bleach, which is a household chemical widely used (since the 18th century) as a disinfectant or a bleaching agent. In solution, the compound is unstable and easily decomposes, liberating chlorine which is the active principle of such products. Sodium hypochlorite is the oldest and still most important chlorine-based bleach. Its corrosive properties, common availability, and reaction products make it a significant safety risk. In particular, mixing liquid bleach with other cleaning products, such as acids or ammonia, may produce toxic fumes. Properties of Sodium Hypochlorite Chemical formula NaOCl Molar mass 74.442 g/mol Appearance greenish-yellow solid (pentahydrate) Odor chlorine-like and sweetish Density 1.11 g/cm3 Melting point 18 °C (64 °F; 291 K) pentahydrate Boiling point 101 °C (214 °F; 374 K) (decomposes) Solubility in water 29.3 g/100mL (0 °C) Acidity (pKa) 7.5185 Basicity (pKb) 6.4815 Chemistry of Sodium hypochlorite Stability of the solid Anhydrous sodium hypochlorite can be prepared but, like many hypochlorites, it is highly unstable and decomposes explosively on heating or friction. The decomposition is accelerated by carbon dioxide at atmospheric levels. It is a white solid with the orthorhombic crystal structure. Sodium hypochlorite can also be obtained as a crystalline pentahydrate NaOCl·5H2O, which is not explosive and is much more stable than the anhydrous compound. The formula is sometimes given as 2NaOCl·10H2O. The transparent light greenish yellow orthorhombic crystals contain 44% NaOCl by weight and melt at 25–27 °C. The compound decomposes rapidly at room temperature, so it must be kept under refrigeration. At lower temperatures, however, it is quite stable: reportedly only 1% decomposition after 360 days at 7 °C. A 1966 US patent claims that stable solid sodium hypochlorite dihydrate NaOCl·2H2O can be obtained by carefully excluding chloride ions (Cl−), which are present in the output of common manufacturing processes and are said to catalyze the decomposition of hypochlorite into chlorate (ClO−3) and chloride. In one test, the dihydrate was claimed to show only 6% decomposition after 13.5 months storage at −25 °C. The patent also claims that the dihydrate can be reduced to the anhydrous form by vacuum drying at about 50 °C, yielding a solid that showed no decomposition after 64 hours at −25 °C. Equilibria and stability of solutions At typical ambient temperatures, sodium hypochlorite is more stable in dilute solutions that contain solvated Na+ and OCl− ions. The density of the solution is 1.093 g/mL at 5% concentration, and 1.21 g/mL at 14%, 20 °C. Stoichiometric solutions are fairly alkaline, with pH 11 or higher since hypochlorous acid is a weak acid: OCl− + H2O ⇌ HOCl + OH− The following species and equilibria are present in solutions of NaOCl: HOCl (aq) ⇌ H+ + OCl−HOCl (aq) + Cl− + H+ ⇌ Cl2 (aq) + H2OCl2 (aq) + Cl− ⇌ Cl−3Cl2 (aq) ⇌ Cl2 (g) The second equilibrium equation above will be shifted to the right if the chlorine Cl2 is allowed to escape as gas. The ratios of Cl2, HOCl, and OCl− in solution are also pH dependent. At pH below 2, the majority of the chlorine in the solution is in the form of dissolved elemental Cl2. At pH greater than 7.4, the majority is in the form of hypochlorite ClO−. The equilibrium can be shifted by adding acids (such as hydrochloric acid) or bases (such as sodium hydroxide) to the solution: ClO− (aq) + 2 HCl (aq) → Cl2 (g) + H2O (aq) + Cl− (aq)Cl2 (g) + 2 OH− → ClO− (aq) + Cl− (aq) + H2O (aq) At a pH of about 4, such as obtained by the addition of strong acids like hydrochloric acid, the amount of undissociated (nonionized) HOCl is highest. The reaction can be written as: ClO− + H+ ⇌ HClO Sodium hypochlorite solutions combined with acid evolve chlorine gas, particularly strongly at pH < 2, by the reactions: HOCl (aq) + Cl− + H+ ⇌ Cl2 (aq) + H2OCl2 (aq) ⇌ Cl2 (g) At pH > 8, the chlorine is practically all in the form of hypochlorite anions (OCl−). The solutions are fairly stable at pH 11–12. Even so, one report claims that a conventional 13.6% NaOCl reagent solution lost 17% of its strength after being stored for 360 days at 7 °C. For this reason, in some applications one may use more stable chlorine-releasing compounds, such as calcium hypochlorite Ca(ClO)2 or trichloroisocyanuric acid (CNClO)3. Anhydrous sodium hypochlorite is soluble in methanol, and solutions are stable. Decomposition to chlorate or oxygen In solution, under certain conditions, the hypochlorite anion may also disproportionate (autoxidize) to chloride and chlorate: 3 ClO− + H+ → HClO3 + 2 Cl− In particular, this reaction occurs in sodium hypochlorite solutions at high temperatures, forming sodium chlorate and sodium chloride: 3 NaOCl (aq) → 2 NaCl (aq) + NaClO3 (aq) This reaction is exploited in the industrial production of sodium chlorate. An alternative decomposition of hypochlorite produces oxygen instead: 2 OCl− → 2 Cl− + O2 In hot sodium hypochlorite solutions, this reaction competes with chlorate formation, yielding sodium chloride and oxygen gas: 2 NaOCl (aq) → 2 NaCl (aq) + O2 (g) These two decomposition reactions of NaClO solutions are maximized at pH around 6. The chlorate-producing reaction predominates at pH above 6, while the oxygen one becomes significant below that. For example, at 80 °C, with NaOCl and NaCl concentrations of 80 mM, and pH 6–6.5, the chlorate is produced with ∼95% efficiency. The oxygen pathway predominates at pH 10. This decomposition is affected by light and metal ion catalysts such as copper, nickel, cobalt, and iridium. Catalysts like sodium dichromate Na2Cr2O7 and sodium molybdate Na2MoO4 may be added industrially to reduce the oxygen pathway, but a report claims that only the latter is effective. Titration Titration of hypochlorite solutions is often done by adding a measured sample to an excess amount of acidified solution of potassium iodide (KI) and then titrating the liberated iodine (I2) with a standard solution of sodium thiosulfate or phenyl arsine oxide, using starch as indicator, until the blue color disappears. According to one US patent, the stability of sodium hypochlorite content of solids or solutions can be determined by monitoring the infrared absorption due to the O–Cl bond. The characteristic wavelength is given as 140.25 μm for water solutions, 140.05 μm for the solid dihydrate NaOCl·2H 2O, and 139.08 μm for the anhydrous mixed salt Na2(OCl)(OH). Oxidation of organic compounds Oxidation of starch by sodium hypochlorite, that adds carbonyl and carboxyl groups, is relevant to the production of modified starch products. In the presence of a phase-transfer catalyst, alcohols are oxidized to the corresponding carbonyl compound (aldehyde or ketone). Sodium hypochlorite can also oxidize organic sulfides to sulfoxides or sulfones, disulfides or thiols to sulfonyl chlorides or bromides, imines to oxaziridines. It can also de-aromatize phenols. Oxidation of metals and complexes Heterogeneous reactions of sodium hypochlorite and metals such as zinc proceed slowly to give the metal oxide or hydroxide: NaOCl + Zn → ZnO + NaCl Homogeneous reactions with metal coordination complexes proceed somewhat faster. This has been exploited in the Jacobsen epoxidation. Other reactions of Sodium hypochlorite If not properly stored in airtight containers, sodium hypochlorite reacts with carbon dioxide to form sodium carbonate: 2 NaOCl + CO2 + H2O → Na2CO3 + 2 HOCl Sodium hypochlorite reacts with most nitrogen compounds to form volatile monochloramine, dichloramines, and nitrogen trichloride: NH3 + NaOCl → NH2Cl + NaOHNH2Cl + NaOCl → NHCl2 + NaOHNHCl2 + NaOCl → NCl3 + NaOH Neutralization Sodium thiosulfate is an effective chlorine neutralizer. Rinsing with a 5 mg/L solution, followed by washing with soap and water, will remove chlorine odor from the hands. Production of Sodium hypochlorite Chlorination of soda Potassium hypochlorite was first produced in 1789 by Claude Louis Berthollet in his laboratory on the Quai de Javel in Paris, France, by passing chlorine gas through a solution of potash lye. The resulting liquid, known as "Eau de Javel" ("Javel water"), was a weak solution of potassium hypochlorite. Antoine Labarraque replaced potash lye by the cheaper soda lye, thus obtaining sodium hypochlorite (Eau de Labarraque). Cl2 (g) + 2 NaOH (aq) → NaCl (aq) + NaClO (aq) + H2O (aq) Hence, chlorine is simultaneously reduced and oxidized; this process is known as disproportionation. The process is also used to prepare the pentahydrate NaOCl·5H 2O for industrial and laboratory use. In a typical process, chlorine gas is added to a 45–48% NaOH solution. Some of the sodium chloride precipitates and is removed by filtration, and the pentahydrate is then obtained by cooling the filtrate to 12 °C . From calcium hypochlorite Another method involved by reaction of sodium carbonate ("washing soda") with chlorinated lime ("bleaching powder"), a mixture of calcium hypochlorite Ca(OCl)2, calcium chloride CaCl2, and calcium hydroxide Ca(OH)2: Na2CO3 (aq) + Ca(OCl)2 (aq) → CaCO3 (s) + 2 NaOCl (aq) Na2CO3 (aq) + CaCl2 (aq) → CaCO3 (s) + 2 NaCl (aq) Na2CO3 (aq) + Ca(OH)2 (s) → CaCO3 (s) + 2 NaOH (aq) This method was commonly used to produce hypochlorite solutions for use as a hospital antiseptic that was sold after World War I under the names "Eusol", an abbreviation for Edinburgh University Solution Of (chlorinated) Lime – a reference to the university's pathology department, where it was developed. Electrolysis of brine Near the end of the nineteenth century, E. S. Smith patented the chloralkali process: a method of producing sodium hypochlorite involving the electrolysis of brine to produce sodium hydroxide and chlorine gas, which then mixed to form sodium hypochlorite. The key reactions are: 2 Cl− → Cl2 + 2 e− (at the anode) 2 H2O + 2 e− → H2 + 2 HO− (at the cathode) Both electric power and brine solution were in cheap supply at the time, and various enterprising marketers took advantage of the situation to satisfy the market's demand for sodium hypochlorite. Bottled solutions of sodium hypochlorite were sold under numerous trade names. Today, an improved version of this method, known as the Hooker process (named after Hooker Chemicals, acquired by Occidental Petroleum), is the only large-scale industrial method of sodium hypochlorite production. In the process, sodium hypochlorite (NaClO) and sodium chloride (NaCl) are formed when chlorine is passed into cold dilute sodium hydroxide solution. The chlorine is prepared industrially by electrolysis with minimal separation between the anode and the cathode. The solution must be kept below 40 °C (by cooling coils) to prevent the undesired formation of sodium chlorate. Commercial solutions always contain significant amounts of sodium chloride (common salt) as the main by-product, as seen in the equation above. From hypochlorous acid and soda A 1966 patent describes the production of solid stable dihydrate NaOCl·2H2O by reacting a chloride-free solution of hypochlorous acid HClO (such as prepared from chlorine monoxide ClO and water), with a concentrated solution of sodium hydroxide. In a typical preparation, 255 mL of a solution with 118 g/L HClO is slowly added with stirring to a solution of 40 g of NaOH in water 0 °C. Some sodium chloride precipitates and is removed by fitration. The solution is vacuum evaporated at 40–50 °C and 1–2 mmHg until the dihydrate crystallizes out. The crystals are vacuum-dried to produce a free-flowing crystalline powder. The same principle was used in another 1991 patent to produce concentrated slurries of the pentahydrate NaClO·5H 2O. Typically, a 35% solution (by weight) of HClO is combined with sodium hydroxide at about or below 25 °C. The resulting slurry contains about 35% NaClO, and are relatively stable due to the low concentration of chloride. From ozone and salt Sodium hypochlorite can be easily produced for research purposes by reacting ozone with salt. NaCl + O3 → NaClO + O2 This reaction happens at room temperature and can be helpful for oxidizing alcohols. Packaging and sale Main article: Bleach Bleach packaged for household use, with 2.6% sodium hypochlorite Household bleach sold for use in laundering clothes is a 3–8% solution of sodium hypochlorite at the time of manufacture. Strength varies from one formulation to another and gradually decreases with long storage. Sodium hydroxide is usually added in small amounts to household bleach to slow down the decomposition of NaClO. A 10–25% solution of sodium hypochlorite is, according to Univar's safety sheet, supplied with synonyms or trade names bleach, Hypo, Everchlor, Chloros, Hispec, Bridos, Bleacol, or Vo-redox 9110. A 12% solution is widely used in waterworks for the chlorination of water, and a 15% solution is more commonly used for disinfection of waste water in treatment plants. Sodium hypochlorite can also be used for point-of-use disinfection of drinking water, taking 0.2-2 mg of sodium hypochlorite per liter of water. Dilute solutions (50 ppm to 1.5%) are found in disinfecting sprays and wipes used on hard surfaces. Uses of Sodium hypochlorite Bleaching Household bleach is, in general, a solution containing 3–8% sodium hypochlorite, by weight, and 0.01–0.05% sodium hydroxide; the sodium hydroxide is used to slow the decomposition of sodium hypochlorite into sodium chloride and sodium chlorate. Cleaning of Sodium hypochlorite Sodium hypochlorite has destaining properties. Among other applications, it can be used to remove mold stains, dental stains caused by fluorosis, and stains on crockery, especially those caused by the tannins in tea. It has also been used in laundry detergents and as a surface cleaner. Its bleaching, cleaning, deodorizing and caustic effects are due to oxidation and hydrolysis (saponification). Organic dirt exposed to hypochlorite becomes water-soluble and non-volatile, which reduces its odor and facilitates its removal. Disinfection of Sodium hypochlorite See also: Hypochlorous acid Sodium hypochlorite in solution exhibits broad spectrum anti-microbial activity and is widely used in healthcare facilities in a variety of settings. It is usually diluted in water depending on its intended use. "Strong chlorine solution" is a 0.5% solution of hypochlorite (containing approximately 5000 ppm free chlorine) used for disinfecting areas contaminated with body fluids, including large blood spills (the area is first cleaned with detergent before being disinfected). It may be made by diluting household bleach as appropriate (normally 1 part bleach to 9 parts water). Such solutions have been demonstrated to inactivate both C. difficile and HPV. "Weak chlorine solution" is a 0.05% solution of hypochlorite used for washing hands, but is normally prepared with calcium hypochlorite granules. "Dakin's Solution" is a disinfectant solution containing low concentration of sodium hypochlorite and some boric acid or sodium bicarbonate to stabilize the pH. It has been found to be effective with NaOCl concentrations as low as 0.025%. US government regulations allow food processing equipment and food contact surfaces to be sanitized with solutions containing bleach, provided that the solution is allowed to drain adequately before contact with food, and that the solutions do not exceed 200 parts per million (ppm) available chlorine (for example, one tablespoon of typical household bleach containing 5.25% sodium hypochlorite, per gallon of water). If higher concentrations are used, the surface must be rinsed with potable water after sanitizing. A similar concentration of bleach in warm water is used to sanitize surfaces prior to brewing of beer or wine. Surfaces must be rinsed with sterilized (boiled) water to avoid imparting flavors to the brew; the chlorinated byproducts of sanitizing surfaces are also harmful. The mode of disinfectant action of sodium hypochlorite is similar to that of hypochlorous acid. Solutions containing more than 500 ppm available chlorine are corrosive to some metals, alloys and many thermoplastics (such as acetal resin) and need to be thoroughly removed afterwards, so the bleach disinfection is sometimes followed by an ethanol disinfection. Liquids containing sodium hypochlorite as the main active component are also used for household cleaning and disinfection, for example toilet cleaners. Some cleaners are formulated to be viscous so as not to drain quickly from vertical surfaces, such as the inside of a toilet bowl. The undissociated (nonionized) hypochlorous acid is believed to react with and inactivate bacterial and viral enzymes. Neutrophils of the human immune system produce small amounts of hypochlorite inside phagosomes, which digest bacteria and viruses. Deodorizing of Sodium hypochlorite Sodium hypochlorite has deodorizing properties, which go hand in hand with its cleaning properties. Waste water treatment of Sodium hypochlorite Sodium hypochlorite solutions have been used to treat dilute cyanide waste water, such as electroplating wastes. In batch treatment operations, sodium hypochlorite has been used to treat more concentrated cyanide wastes, such as silver cyanide plating solutions. Toxic cyanide is oxidized to cyanate (OCN−) that is not toxic, idealized as follows: CN− + OCl− → OCN− + Cl− Sodium hypochlorite is commonly used as a biocide in industrial applications to control slime and bacteria formation in water systems used at power plants, pulp and paper mills, etc., in solutions typically of 10–15% by weight. Endodontics Sodium hypochlorite is the medicament of choice due to its efficacy against pathogenic organisms and pulp digestion in endodontic therapy. Its concentration for use varies from 0.5% to 5.25%. At low concentrations it dissolves mainly necrotic tissue; at higher concentrations it also dissolves vital tissue and additional bacterial species. One study has shown that Enterococcus faecalis was still present in the dentin after 40 minutes of exposure of 1.3% and 2.5% sodium hypochlorite, whereas 40 minutes at a concentration of 5.25% was effective in E. faecalis removal. In addition to higher concentrations of sodium hypochlorite, longer time exposure and warming the solution (60 °C) also increases its effectiveness in removing soft tissue and bacteria within the root canal chamber. 2% is a common concentration as there is less risk of an iatrogenic hypochlorite incident. A hypochlorite incident is an immediate reaction of severe pain, followed by edema, haematoma, and ecchymosis as a consequence of the solution escaping the confines of the tooth and entering the periapical space. This may be caused by binding or excessive pressure on the irrigant syringe, or it may occur if the tooth has an unusually large apical foramen. Nerve agent neutralization At the various nerve agent (chemical warfare nerve gas) destruction facilities throughout the United States, 50% sodium hypochlorite is used to remove all traces of nerve agent or blister agent from Personal Protection Equipment after an entry is made by personnel into toxic areas. 50% sodium hypochlorite is also used to neutralize any accidental releases of nerve agent in the toxic areas. Lesser concentrations of sodium hypochlorite are used in similar fashion in the Pollution Abatement System to ensure that no nerve agent is released in furnace flue gas. Reduction of skin damage Dilute bleach baths have been used for decades to treat moderate to severe eczema in humans, but it has not been clear why they work. According to work published by researchers at the Stanford University School of Medicine in November 2013, a very dilute (0.005%) solution of sodium hypochlorite in water was successful in treating skin damage with an inflammatory component caused by radiation therapy, excess sun exposure or aging in laboratory mice. Mice with radiation dermatitis given daily 30-minute baths in bleach solution experienced less severe skin damage and better healing and hair regrowth than animals bathed in water. A molecule called nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) is known to play a critical role in inflammation, aging, and response to radiation. The researchers found that if NF-κB activity was blocked in elderly mice by bathing them in bleach solution, the animals' skin began to look younger, going from old and fragile to thicker, with increased cell proliferation. The effect diminished after the baths were stopped, indicating that regular exposure was necessary to maintain skin thickness. Safety It is estimated that there are about 3,300 accidents needing hospital treatment caused by sodium hypochlorite solutions each year in British homes (RoSPA, 2002). Oxidation and corrosion Sodium hypochlorite is a strong oxidizer. Oxidation reactions are corrosive. Solutions burn the skin and cause eye damage, especially when used in concentrated forms. As recognized by the NFPA, however, only solutions containing more than 40% sodium hypochlorite by weight are considered hazardous oxidizers. Solutions less than 40% are classified as a moderate oxidizing hazard (NFPA 430, 2000). Household bleach and pool chlorinator solutions are typically stabilized by a significant concentration of lye (caustic soda, NaOH) as part of the manufacturing reaction. This additive will by itself cause caustic irritation or burns due to defatting and saponification of skin oils and destruction of tissue. The slippery feel of bleach on skin is due to this process. Storage hazards Contact of sodium hypochlorite solutions with metals may evolve flammable hydrogen gas. Containers may explode when heated due to release of chlorine gas. Hypochlorite solutions are corrosive to common container materials such as stainless steel and aluminium. The few compatible metals include titanium (which however is not compatible with dry chlorine) and tantalum. Glass containers are safe. Some plastics and rubbers are affected too; safe choices include polyethylene (PE), high density polyethylene (HDPE, PE-HD), polypropylene (PP), some chlorinated and fluorinated polymers such as polyvinyl chloride (PVC), polytetrafluoroethylene (PTFE), and polyvinylidene fluoride (PVDF); as well as ethylene propylene rubber, and Viton. Containers must allow venting of oxygen produced by decomposition over time, otherwise they may burst. Reactions with other common products Mixing bleach with some household cleaners can be hazardous. Sodium hypochlorite solutions, such as liquid bleach, may release toxic chlorine gas when heated above 35 °C or mixed with an acid, such as hydrochloric acid or vinegar. A 2008 study indicated that sodium hypochlorite and organic chemicals (e.g., surfactants, fragrances) contained in several household cleaning products can react to generate chlorinated volatile organic compounds (VOCs). These chlorinated compounds are emitted during cleaning applications, some of which are toxic and probable human carcinogens. The study showed that indoor air concentrations significantly increase (8–52 times for chloroform and 1–1170 times for carbon tetrachloride, respectively, above baseline quantities in the household) during the use of bleach containing products. The increase in chlorinated volatile organic compound concentrations was the lowest for plain bleach and the highest for the products in the form of "thick liquid and gel." The significant increases observed in indoor air concentrations of several chlorinated VOCs (especially carbon tetrachloride and chloroform) indicate that the bleach use may be a source that could be important in terms of inhalation exposure to these compounds. The authors suggested that using these cleaning products may significantly increase the cancer risk. In particular, mixing hypochlorite bleaches with amines (for example, cleaning products that contain or release ammonia, ammonium salts, urea, or related compounds and biological materials such as urine) produces chloramines. These gaseous products can cause acute lung injury. Chronic exposure, for example, from the air at swimming pools where chlorine is used as the disinfectant, can lead to the development of atopic asthma. Bleach can react violently with hydrogen peroxide and produce oxygen gas: H2O2 (aq) + NaOCl (aq) → NaCl (aq) + H2O (aq) + O2 (g) Explosive reactions or byproducts can also occur in industrial and laboratory settings when sodium hypochlorite is mixed with diverse organic compounds. Limitations in health care The UK's National Institute for Health and Care Excellence in October 2008 recommended that Dakin's solution should not be used in routine wound care. Environmental impact In spite of its strong biocidal action, sodium hypochlorite per se has limited environmental impact, since the hypochlorite ion rapidly degrades before it can be absorbed by living beings. However, one major concern arising from sodium hypochlorite use is that it tends to form persistent chlorinated organic compounds, including known carcinogens, that can be absorbed by organisms and enter the food chain. These compounds may be formed during household storage and use as well during industrial use. For example, when household bleach and wastewater were mixed, 1–2% of the available chlorine was observed to form organic compounds. As of 1994, not all the byproducts had been identified, but identified compounds include chloroform and carbon tetrachloride. The estimated exposure to these chemicals from use is estimated to be within occupational exposure limits. Sodium hypochlorite (NaOCl) is a compound that can be effectively used for water purification. It is used on a large scale for surface purification, bleaching, odor removal and water disinfection. When was sodium hypochlorite discovered? Sodium hypochlorite has a long history. Around 1785 the Frenchman Berthollet developed liquid bleaching agents based on sodium hypochlorite. The Javel company introduced this product and called it 'liqueur de Javel'. At first, it was used to bleach cotton. Because of its specific characteristics it soon became a popular compound. Hypochlorite can remove stains from clothes at room temperature. In France, sodium hypochlorite is still known as 'eau de Javel'. What are the characteristics of sodium hypochlorite? Sodium hypochlorite is a clear, slightly yellowish solution with a characteristic odor. Sodium hypochlorite has a relative density of is 1,1 (5,5% watery solution). As a bleaching agent for domestic use it usually contains 5% sodium hypochlorite (with a pH of around 11, it is irritating). If it is more concentrated, it contains a concentration 10-15% sodium hypochlorite (with a pH of around 13, it burns and is corrosive). Sodium hypochlorite is unstable. Chlorine evaporates at a rate of 0,75 gram active chlorine per day from the solution. Then heated sodium hypochlorite disintegrates. This also happens when sodium hypochlorite comes in contact with acids, sunlight, certain metals and poisonous and corrosive gasses, including chlorine gas. Sodium hypochlorite is a strong oxidator and reacts with flammable compounds and reductors. Sodium hypochlorite solution is a weak base that is inflammable. These characteristics must be kept in mind during transport, storage and use of sodium hypochlorite. What happens to the pH value when sodium hypochlorite is added to water? Due to the presence of caustic soda in sodium hypo chlorite, the pH of the water is increased. When sodium hypo chlorite dissolves in water, two substances form, which play a role in for oxidation and disinfection. These are hypochlorous acid (HOCl) and the less active hypochlorite ion (OCl-). The pH of the water determines how much hypochlorous acid is formed. While sodium hypochlorite is used, hydrochloric acid (HCl) is used to lower the pH. Sulfuric acid (H2SO4) can be used as an alternative for acetic acid. Less harmful gasses are produced when sulfuric acid is used. Sulfuric acid is a strong acid that strongly reacts with bases and that is very corrosive. How can sodium hypochlorite be produced? Sodium hypochlorite can be produced in two ways: - By dissolving salt in softened water, which results in a concentrated brine solution. The solution is electrolyzed and forms a sodium hypochlorite solution in water. This solution contains 150 g active chlorine (Cl2) per liter. During this reaction the explosive hydrogen gas is also formed. - By adding chlorine gas (Cl2) to caustic soda (NaOH). When this is done, sodium hypochlorite, water (H2O) and salt (NaCl) are produced according to the following reaction: Cl2 + 2NaOH + → NaOCl + NaCl + H2O What are the applications of sodium hypochlorite? Sodium hypochlorite is used on a large scale. For example in agriculture, chemical industries, paint- and lime industries, food industries, glass industries, paper industries, pharmaceutical industries, synthetics industries and waste disposal industries. In the textile industry sodium hypochlorite is used to bleach textile. It is sometimes added to industrial waste water. This is done to reduce odors. Hypochlorite neutralizes sulphur hydrogen gas (SH) and ammonia (NH3). It is also used to detoxify cyanide baths in metal industries. Hypochlorite can be used to prevent algae and shellfish growth in cooling towers. In water treatment, hypochlorite is used to disinfect water. In households, hypochlorite is used frequently for the purification and disinfection of the house. How does sodium hypochlorite disinfection work? By adding hypochlorite to water, hypochlorous acid (HOCl) is formed: NaOCl + H2O → HOCl + NaOH- Hypochlorous acid is divided into hydrochloric acid (HCl) and oxygen (O). The oxygen atom is a very strong oxidator. Sodium hypochlorite is effective against bacteria, viruses and fungi. Sodium hypochlorite disinfects the same way as chlorine does. How is sodium hypochlorite applied in swimming pools? Sodium hypochlorite is applied in swimming pools for water disinfection and oxidation. It has the advantage that microorganisms cannot build up any resistance to it. Sodium hypochlorite is effective against Legionella bacteria and bio film, in which Legionella bacteria can multiply. Hypochlorous acid is produced by the reaction of sodium hydroxide with chlorine gas. In water, the so-called 'active chlorine' is formed. There are various ways to use sodium hypochlorite. For on-site salt electrolysis, a solution of salt (NaCl) in water is applied. Sodium (Na+) and chloride (Cl-) ions are produced. 4NaCl- → 4Na+ + 4Cl- By leading the salty solution over an electrolysis cell, the following reactions take place at the electrodes: 2Cl- → Cl2 + 2e- 2H2O + 2e- → H2 + 20H- 2H20 → O2 + 4H++ 4e- Subsequently, chlorine and hydroxide react to form hypochlorite: OH- + Cl2 → HOCl + Cl- The advantage of the salt electrolysis system is that no transport or storage of sodium hypochlorite is required. When sodium hypochlorite is stored for a long time, it becomes inactive. Another advantage of the on site process is that chlorine lowers the pH and no other acid is required to lower pH. The hydrogen gas that is produced is explosive and as a result ventilation is required for expolsion prevention. This system is slow and a buffer of extra hypochlorous acid needs to be used. The maintenance and purchase of the electrolysis system is much more expensive than sodium hypochlorite. When sodium hypochlorite is used, acetic or sulphuric acid are added to the water. An overdose can produce poisonous gasses. If the dosage is too low, the pH becomes to high and can irritate the eyes. Because sodium hypochlorite is used both to oxidize pollutions (urine, sweat, cosmetics) and to remove pathogenic microorganisms, the required concentration of sodium hypochlorite depends on the concentrations of these pollutions. Especially the amount of organic pollution determines the required concentration. If the water is filtered before sodium hypochlorite is applied, less sodium hypochlorite is needed.
SODIUM ISETHIONATE
SODIUM ISOBUTYLPARABEN N° CAS : 84930-15-4 Origine(s) : Synthétique Nom INCI : SODIUM ISOBUTYLPARABEN Nom chimique : Sodium isobutyl 4-oxidobenzoate N° EINECS/ELINCS : 284-595-4 Classification : Paraben, Perturbateur endocrinien suspecté, Règlementé, Conservateur, Interdit en Europe Restriction en Europe : II/1375 La concentration maximale autorisée dans les préparations cosmétiques prêtes à l'emploi est de : - 0,4 % (en acide) pour un ester - 0,8 % (en acide) pour les mélanges d'esters Ses fonctions (INCI) Antimicrobien : Aide à ralentir la croissance de micro-organismes sur la peau et s'oppose au développement des microbes
SODIUM ISOBUTYLPARABEN
SODIUM ISOSTEARATE N° CAS : 64248-79-9 Nom INCI : SODIUM ISOSTEARATE Nom chimique : Isooctadecanoic acid, sodium salt N° EINECS/ELINCS : 264-754-4 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) Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM ISOSTEARATE
SODIUM LACTATE; N° CAS : 72-17-3 / 867-56-1 - Lactate de sodium; Nom INCI : SODIUM LACTATE; Nom chimique : Sodium lactate; N° EINECS/ELINCS : 200-772-0 / 212-762-3; Additif alimentaire : E325. Compatible Bio (Référentiel COSMOS). Ses fonctions (INCI). Régulateur de pH : Stabilise le pH des cosmétiques. Humectant : Maintient la teneur en eau d'un cosmétique dans son emballage et sur la peau; Kératolytique : Décolle et élimine les cellules mortes de la couche cornée de l'apiderme. Noms français : 2-HYDROXYPROPANOATE SODIUM; HYDROXY-2 PROPANOATE DE SODIUM; Lactate de sodium; PROPANOIC ACID, 2-HYDROXY-, MONOSODIUM SALT; SEL DE SODIUM DE L'ACIDE HYDROXY-2 PROPANOIQUE. Noms anglais : LACTIC ACID SODIUM SALT; LACTIC ACID, MONOSODIUM SALT; LACTIC ACID, SODIUM SALT; Sodium lactate. Utilisation et sources d'émission: Agent anticorrosif. 2-Hydroxypropanoic acid, monosodium salt; Lacolin; Lactic acid sodium salt; Lactic acid, monosodium salt; Lactic acid, sodium salt (VAN); Monosodium 2-hydroxypropanoate; Monosodium lactate; Per-glycerin; Propanoic acid, 2-hydroxy-, monosodium salt; Propanoic acid, 2-hydroxy-, sodium salt (1:1); Sodium (dl)-lactate; Sodium alpha-hydroxypropionate; Sodium lactate; Sodium lactate 0.167 molar in plastic container; Sodium lactate 1/6 molar in plastic container; Sodium lactate in plastic container. IUPAC names: Sodium 2-hydroxy-propanoate; Sodium 2-hydroxypropanoate;Sodium DL-lactate ; sodium;2-hydroxypropanoate; (±)-2-Hydroxypropionic acid sodium salt; 200-772-0 [EINECS]; 2-Hydroxypropanoate de sodium [French] ; 4157; 72-17-3 [RN]; Lactic acid monosodium salt Lactic Acid, Sodium Salt; MFCD00065400 [MDL number]; Natrium-2-hydroxypropanoat [German]; Propanoic acid, 2-hydroxy-, sodium salt (1:1) [ACD/Index Name]; QY1&VQ &&Na salt [WLN] ; Sodium 2-hydroxypropanoate [ACD/IUPAC Name]; Sodium Lactate [JAN] [USAN]; SODIUM LACTATE, L-; Sodium α-hydroxypropionate; Sodium-DL-lactate; [72-17-3];1219802-24-0 [RN] ; 2-Hydroxypropanoic acid, monosodium salt; 2-Hydroxypropionic acid sodium salt; 344299-52-1 [RN]; E325; Lacolin; Lactic acid, monosodium salt (8CI); Lactic acid, sodium salt (VAN) ; MFCD00066576 [MDL number]; Monosodium 2-hydroxypropanoate; P2Y1C6M9PS; Per-glycerin; Pharmakon1600-01300036; Propanoic acid, 2-hydroxy-, monosodium salt; Propanoic acid, 2-hydroxy-, monosodium salt (9CI); Purasal S/SP 60; Sodium (dl)-lactate; Sodium lactate (60% in water); Sodium lactate (7CI); SODIUM LACTATE|SODIUM 2-HYDROXYPROPANOATE ; SODIUM α-HYDROXYPROPIONATE; sodiumlactate; SodiumLactate,(??)-2-Hydroxypropionicacidsodiumsalt,SodiumDL-lactate,Lacolin?; 乳酸ナトリウム [Japanese]
SODIUM LACTATE ( Lactate de sodium)
cas no 867-56-1 (S)-2-Hydroxypropionic acid sodium salt; L-Lactic acid sodium salt; Sarcolactic acid sodium salt; Sodium L-lactate; Sodium L-lactate;
SODIUM LACTATE POWDER
SYNONYMS Disodium monosulfate; Sulfuric acid sodium salt;Disodium sulfate; Sodium sulfate; Sulfuric acid sodium salt; Sulfuric acid disodium salt; Sulfuric acid disodium salt; Salt cake; Bisodium sulfate; Sodium sulfate (2:1); Thenardite; Natriumsulfat; Trona; Dibasic sodium sulfate; CAS NO:7757-82-6
SODIUM LAURETH-11 CARBOXYLATE
SODIUM LAURETH-12 CARBOXYLATE N° CAS : 33939-64-9 Nom INCI : SODIUM LAURETH-12 CARBOXYLATE Classification : Composé éthoxylé Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre
SODIUM LAURETH-12 CARBOXYLATE
SODIUM LAURETH-12 SULFATE N° CAS : 9004-82-4 Nom INCI : SODIUM LAURETH-12 SULFATE N° EINECS/ELINCS : 266-192-5 Classification : Sulfate, Composé éthoxylé Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM LAURETH-12 SULFATE
SODIUM LAURETH-4 CARBOXYLATE N° CAS : 33939-64-9 / 38975-04-1 Nom INCI : SODIUM LAURETH-4 CARBOXYLATE N° EINECS/ELINCS : - / - Classification : Composé éthoxylé Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM LAURETH-4 CARBOXYLATE
SODIUM LAURETH-4 PHOSPHATE N° CAS : 42612-52-2 Nom INCI : SODIUM LAURETH-4 PHOSPHATE Classification : Composé éthoxylé 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) Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM LAURETH-4 PHOSPHATE
SODIUM LAURETH-5 CARBOXYLATE N° CAS : 33939-64-9 / 38975-03-0 "Pas terrible" dans toutes les catégories. Nom INCI : SODIUM LAURETH-5 CARBOXYLATE N° EINECS/ELINCS : - / - Classification : Composé éthoxylé Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM LAURETH-5 CARBOXYLATE
SODIUM LAURETH-6 CARBOXYLATE N° CAS : 33939-64-9 "Pas terrible" dans toutes les catégories. Nom INCI : SODIUM LAURETH-6 CARBOXYLATE Classification : Composé éthoxylé Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM LAURETH-6 CARBOXYLATE
SODIUM LAURETH-7 SULFATE N° CAS : 9004-82-4 Nom INCI : SODIUM LAURETH-7 SULFATE Classification : Sulfate, Composé éthoxylé Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM LAURETH-7 SULFATE
SODIUM LAURETH-8 SULFATE N° CAS : 9004-82-4 Nom INCI : SODIUM LAURETH-8 SULFATE Classification : Sulfate, Composé éthoxylé Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM LAURETH-8 SULFATE
SODIUM LAURIMINODIPROPIONATE N° CAS : 14960-06-6 / 26256-79-1 Nom INCI : SODIUM LAURIMINODIPROPIONATE Nom chimique : Sodium N-(2-carboxyethyl)-N-dodecyl-.beta.-alaninate N° EINECS/ELINCS : 239-032-7 / 247-552-0 Ses fonctions (INCI) Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface Agent nettoyant : Aide à garder une surface propre Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide 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 Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM LAURIMINODIPROPIONATE
SODIUM LAUROAMPHOACETATE; N° CAS : 66161-62-4; Nom INCI : SODIUM LAUROAMPHOACETATE. Nom chimique : Glycine, N-(2-hydroxyethyl)-N-[2-(1-oxododecylamino)ethyl]-, monosodium salt; N° EINECS/ELINCS : 266-197-2. Compatible Bio (Référentiel COSMOS). Ses fonctions (INCI): Agent nettoyant : Aide à garder une surface propre; Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide. 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. Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : N-(2-hydroxyéthyl)-N-[2-[(1-oxododécyl)amino]éthyl]glycinate de sodium. Noms anglais : 2-LAURYLAMIDO-N-HYDROXYETHYL-N-(SODIUM CARBOXYMETHYL)ETHYLAMINE; GLYCINE, N-(2-HYDROXYETHYL)-N-(2-((1-OXODODECYL)AMINO)ETHYL)-, MONOSODIUM SALT; Sodium N-(2-hydroxyethyl)-N-[2-[(1-oxododecyl)amino]ethyl]glycinate; sodium 2-[(2-dodecanamidoethyl)(2-hydroxyethyl)amino]acetate; {[2-(Dodecanoylamino)éthyl](2-hydroxyéthyl)amino}acétate de sodium [French] [ACD/IUPAC Name]; 266-197-2 [EINECS]; 66161-62-4 [RN]; Glycine, N-(2-hydroxyethyl)-N-[2-[(1-oxododecyl)amino]ethyl]-, sodium salt (1:1) [ACD/Index Name]; Natrium-{[2-(dodecanoylamino)ethyl](2-hydroxyethyl)amino}acetat [German] [ACD/IUPAC Name]; Sodium {[2-(dodecanoylamino)ethyl](2-hydroxyethyl)amino}acetate [ACD/IUPAC Name]; Sodium lauroamphoacetate; 108538-32-5 [RN]; 2-Laurylamido-N-hydroxyethyl-N-(sodium carboxymethyl)ethylamine EINECS 266-197-2; Glycine, N-(2-hydroxyethyl)-N-(2-((1-oxododecyl)amino)ethyl)-, monosodium salt; Glycine, N-(2-hydroxyethyl)-N-[2-[(1-oxododecyl)amino]ethyl]-, monosodium salt ; Glycine,N-(2-hydroxyethyl)-N-[2-[(1-oxododecyl)amino]ethyl]-, sodium salt (1:1); SODIUM 2-[(2-DODECANAMIDOETHYL)(2-HYDROXYETHYL)AMINO]ACETATE; sodium 2-[2-(dodecanoylamino)ethyl-(2-hydroxyethyl)amino]acetate; sodium 2-[2-(dodecanoylamino)ethyl-(2-hydroxyethyl)amino]ethanoate; sodium 2-[2-hydroxyethyl-[2-(1-oxododecylamino)ethyl]amino]acetate; sodium 2-[2-hydroxyethyl-[2-(lauroylamino)ethyl]amino]acetate; Sodium N-(2-hydroxyethyl)-N-(2-((1-oxododecyl)amino)ethyl)glycinate; sodium N-(2-hydroxyethyl)-N-[2-[(1-oxododecyl)amino]ethyl]glycinate
SODIUM LAUROAMPHOACETATE
cas no 29923-31-7 N-(1-Oxododecyl)-L-glutamic acid monosodium salt; N-Lauroyl-L-glutamic acid monosodium salt; Sodium N-dodecanoylglutamate; Sodium lauroyl glutamate; Monosodium N-lauroyl-L-glutamate;
SODIUM LAUROYL GLUTAMATE
SODIUM LAUROYL GLUTAMATE; N° CAS : 29923-31-7 / 29923-34-0 / 42926-22-7 / 98984-78-2. Origine(s) : Végétale, Synthétique; Nom INCI : SODIUM LAUROYL GLUTAMATE; Nom chimique : Sodium hydrogen N-(1-oxododecyl)-L-glutamate; N° EINECS/ELINCS : 249-958-3 / - / - / -. Classification : Tensioactif non ionique. Compatible Bio (Référentiel COSMOS). Ses fonctions (INCI) ; Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface; Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance; Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation; Lauroyl-L-glutamate-Na, N- sodium hydrogen (2S)-2-dodecanamidopentanedioate; sodium hydrogen 2-(dodecanoylamino)pentanedioate; sodium hydrogen N-(1-oxododecyl)-L-glutamate CAS information ?; Sodium hydrogen N-(1-oxododecyl)-L-glutamate/Sodium Lauroyl Glutamate; Sodium Lauroyl Glutamate; Sodium hydrogen N-(1-oxododecyl)-L-glutamate
SODIUM LAUROYL GLYCINATE
SODIUM LAUROYL ISETHIONATE N° CAS : 7381-01-3 Nom INCI : SODIUM LAUROYL ISETHIONATE Nom chimique : Sodium 2-sulphonatoethyl laurate N° EINECS/ELINCS : 230-949-8 Ses fonctions (INCI) Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface Agent nettoyant : Aide à garder une surface propre Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance Agent d'entretien de la peau : Maintient la peau en bon état Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM LAUROYL ISETHIONATE
SODIUM LAUROYL METHYL ISETHIONATE, Origine(s) : Végétale, Synthétique, Nom INCI : SODIUM LAUROYL METHYL ISETHIONATE. Nom chimique : Dodecanoic acid, methyl-2-sulfoethyl ester, sodium salt (1:1). Le Sodium Lauroyl Methyl Isethionate ou SLMI est un tensioactif anionique doux dérivé de coco, qui ne contient pas de sulfate. Contrairement au SCI (Sodium Cocoyl Isethionate) qui permet de créer des produits opaques, le SLMI a une excellente solubilité dans l'eau, et permet donc de créer des formulations de shampooings sans sulfate, transparente. Il est souvent utilisé conjointement avec de la CAPB.Ses fonctions (INCI) : Agent nettoyant : Aide à garder une surface propre. Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM LAUROYL METHYL ISETHIONATE
Sodium lauroylsarcosinate; SODIUM LAUROYL SARCOSINATE; N° CAS : 137-16-6; Origine(s) : Végétale, Synthétique; Nom INCI : SODIUM LAUROYL SARCOSINATE; Nom chimique : Sodium N-lauroylsarcosinate; N° EINECS/ELINCS : 205-281-5. Classification : Tensioactif anionique. Le sodium Lauroyl Sarconisate est un tensioactif anionique bien plus doux que les composés sulfatés. Dérivé d'acide gras et d'amine naturelle, il entre dans la composition de produits lavants doux et est aussi utilisé dans les dentifrices.Ses fonctions (INCI). Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. 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). Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Agent d'entretien de la peau : Maintient la peau en bon état. Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques; Noms français : GLYCINE, N-METHYL-N-(1-OXODODECYL)-, SODIUM SALT; Lauroylsarcosinate de sodium; N-lauroylsarcosinate de sodium; Noms anglais : SODIUM N-LAUROYLSARCOSINATE. Utilisation: Agent antiseptique; Sodium N-lauroylsarcosinate; CAS names: Glycine, N-methyl-N-(1-oxododecyl)-, sodium salt (1:1); IUPAC names: 2-[dodecanoyl(methyl)amino]acetic acid; sodium; N-Dodecanoyl-N-methylglycine sodium salt, Sarkosyl NL, Sodium lauroyl sarcosinate; N-Methyl-N-(1-Oxododecyl)Glycine, Sodium Salt; sodium 2-(N-methyldodecanamido)acetate; sodium 2-[dodecanoyl(methyl)amino]acetate; sodium [dodecanoyl(methyl)amino]acetate; SODIUM LAUROYL SARCOSINATE; Sodium Lauryl Sarconinate; Sodium N-lauroylsarcosinate/Sodium lauroylsarcosinate; N-Lauroylsarcosine sodium salt; [Dodecanoyl(méthyl)amino]acétate de sodium [French] 137-16-6 [RN] 205-281-5 [EINECS] 5322974 Glycine, N-methyl-N- (1-oxododecyl)-, sodium salt Glycine, N-methyl-N-(1-oxododecyl)-, sodium salt (1:1) [ACD/Index Name] MFCD00042728 Natrium-[dodecanoyl(methyl)amino]acetat [German] [ACD/IUPAC Name] N-Dodecanoyl-N-methylglycine sodium salt N-Lauroylsarcosine sodium salt solution N-Methyl-N-(1-oxododecyl)glycine Sodium Salt Sarcosine, N-lauroyl-, sodium salt Sarcosyl Sarcosyl NL Sarkosyl NL Sodium [dodecanoyl(methyl)amino]acetate [ACD/IUPAC Name] SODIUM LAUROYL SARCOSINATE Sodium lauroylsarcosinate Sodium N-dodecanoyl-N-methylglycinate SODIUM N-LAUROYL SARCOSINATE Sodium N-lauroylsarcosinate Sodium N-lauroylsarcosinate solution [137-16-6] 2-(N-methyldodecanoylamino)acetic acid, sodium salt EINECS 205-281-5 Gardol Gardol? Glycine, N-methyl-N-(1-oxododecyl)-, sodium salt Hamposyl L-30 Lauroylsarcosine sodium salt Maprosyl 30 Medialan LL-99 N-Dodecanoyl-N-methylglycine, sodium salt N-Dodecanoyl-N-methylglycinesodium salt N-LAUROYL-N-METHYLGLYCINE SODIUM SALT N-Lauroylsarcosine sodium salt, 10% solution N-Lauroylsarcosine sodium salt, 30% solution N-Lauroylsarcosine, sodium N-Lauroylsarcosine, sodium salt N-Lauroylsarcosinesodium salt N-Lauryl sarcosine sodium salt N-Methyl-N-(1-oxododecyl)glycine, sodium salt Sarcosine, N-lauroyl-, sodium salt (8CI) Sarkosyl sodium 2-(dodecanoyl-methylamino)acetate sodium 2-(dodecanoyl-methyl-amino)acetate sodium 2-(dodecanoyl-methyl-amino)ethanoate sodium 2-(lauroyl-methyl-amino)acetate sodium 2-(methyl-(1-oxododecyl)amino)acetate Sodium 2-(N-methyldodecanamido)acetate Sodium lauroylsarcosine Sodium N-Lauroylsarcosinate|N-Dodecanoylsarcosine Sodium Salt|N-Lauroylsarcosine Sodium Salt SODIUM N-LAUROYLSARCOSINE sodium[dodecanoyl(methyl)amino]acetate
SODIUM LAUROYL SARCOSINATE ( Lauroylsarcosinate de sodium )
SODIUM LAURYL ASPARTATE N° CAS : 267653-39-4 Nom INCI : SODIUM LAURYL ASPARTATE Nom chimique : Aspartic acid, N-dodecyl-, monosodium salt Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
SODIUM LAURYL ASPARTATE
cas no 3088-31-1 Soudium POE(2) Lauryl Ether Sulfate; Soudium Diethylene Glycol Lauryl Ether Sulfate; Sodium Lauryl Ether Sulfate; 2-(2-dodecyloxyethoxy)Ethyl Sodium Sulfate; Diethylene Glycol Monododecyl Ether Sulfate Sodium Salt; Lauristyl Diglycol Ether Sulfate Sodium Salt; Lauryl Diethylene Glycol Ether Sulfonate Sodium; Sodium Dioxyethylenedodecyl Ether Sulfate; Sodium Lauryl Alcohol Diglycol Ether Sulfate; Sodium Lauryloxyethoxyethyl Sulfate; Sodiumlaurylglycolether Sulfate; Natrium-2-(2-dodecyloxyethoxy)ethylsulfat (German); Sulfato de sodio y 2-(2-dodeciloxietoxi)etilo (Spanish); Ssulfate de sodium et de 2-(2-dodécyloxyethoxy)éthyle (French);
SODIUM LAURYL GLUCOSE CARBOXYLATE
SODIUM LAURYL GLUCOSE CARBOXYLATE Sodium lauryl glucose carboxylate Derived from: coconut Pronunciation: (\ˈsō-dē-əm\ˈlȯr-əl \ˈglü-ˌkōs \car·box·yl·ate\) Type: Naturally-derived What Is Sodium lauryl glucose carboxylate? Sodium lauryl glucose carboxylate is a yellow liquid derived from coconut. Coconuts grow on the cocos nucifera, or coconut palm tree, around the world in lowland tropical and subtropical areas where annual precipitation is low. Widely cultivated, healthy coconut palms produce 50 nuts per year, and the tree can be used to produce everything from food and drink to fibers, building materials, and natural ingredients. What Does Sodium lauryl glucose carboxylate Do in Our products? Sodium lauryl glucose carboxylate is a surfactant that allows water, oil and dirt to mix, allowing things to become clean. It is also a foam booster and conditioning agent.[6] It can be found in personal care products such as shampoo, body wash, facial cleanser, exfoliants, makeup remover, and other items.[7] Why Puracy Uses Sodium lauryl glucose carboxylate We use sodium lauryl glucose carboxylate as a biodegradable surfactant and cleanser. Whole Foods has deemed the ingredient acceptable in its body care quality standards.[9] Research shows the ingredient is typically not a strong skin irritant or sensitizer.[10,11,12] How Sodium lauryl glucose carboxylate Is Made Sodium lauryl glucose carboxylate is an alkyl polyglucoside made by reacting corn starch with a fatty alcohol to produce a highly biodegradable surfactant. We try to be careful about what we put on our skin. We purchase products from reputable companies. We read ingredient labels, and avoid anything that sounds too chemical or harsh. But there are exceptions to the rules. Sometimes our first instincts are wrong. Take the following two ingredients, for example: Sodium lauryl sulfate Sodium lauryl glucose carboxylate They look similar, right? And they both look, well, chemical. Which means bad, right? Not necessarily. In fact, one of these ingredients is a sheep in wolf’s clothing, and a very good-for-your-skin sheep at that. Do you know which one? What is Sodium Lauryl Sulfate? This is a common ingredient in cleansing products. You’re likely to see it in standard brands of facial cleansers, body washes, shampoos, and other similar items. Called “SLS” for short, it’s a surfactant made by treating lauryl alcohol (from coconut or palm kernel oil) with sulfur trioxade gas, oleum (fuming sulfuric acid), or chlorosulfuric acid to produce hydrogen lauryl sulfate, which is then neutralized with sodium hydroxide or sodium carbonate to produce SLS. This product is an effective cleanser but is too harsh and irritating for skin. It’s highly corrosive, which means it can remove oil and grease—but do you want that effect on your skin? Despite its irritating nature, it’s used in the cosmetic industry as well as in laundry products, engine degreasers, carpet cleaners, car wash soaps, and in other industrial cleaning applications. Studies have verified that this ingredient can be damaging. In the International Journal of Toxicology, researchers noted that it had a “degenerative effect on the cell membranes because of its protein denaturing properties,” and that it could cause skin irritation and corrosion. Researchers later wrote, “The longer these ingredients stay in contact with the skin, the greater the likelihood of irritation, which may or may not be evident to the user.” They add in their discussion of the study that the ingredient was found to cause “severe epidermal changes” where it was applied, and that it could also damage the hair follicle (when used in hair-care products). Even worse—a solution containing a 1-5 percent sodium lauryl sulfate caused acne! The researchers wrote: “These two problems—possible hair loss and comedone [pimple] formation—along with proven irritancy, should be considered in the formulation of cosmetic products.” Their conclusion was that as long as SLS is included at less than one percent and is rinsed off immediately, it appears to be safe. That’s not good enough for most of our customers, especially considering that we use cleansing products a couple times a day, every day, for most of our lives. This is an ingredient that with repeated use can cause hair and skin damage. So the first ingredient is definitely a no-no. But what about the second — sodium lauryl glucoside carboxylate? What is Sodium Lauryl Glucose Carboxylate? This ingredient has to be similar to SLS, right? Potentially just as damaging? Nope. And this is where skin care can get confusing. It’s a similar name, and it’s also a cleaning ingredient, but it’s much nicer to skin. To begin with, it lacks the “sulfate” part of the name, which identifies an ingredient as a salt of sulfuric acid. We don’t have any acid going on in this ingredient. So goodbye harsh irritant! Lauryl glucoside belongs to a class of ingredients called “glucosides” which are made by bonding the base group with sugar (instead of sulfuric acid). Salicylic acid, for example (found in oily skin care products), comes from salicin, which is a glucoside—a combination of salicyl alcohol and glucose (and found naturally in willow bark). To make sodium lauryl glucose carboxylate, lauryl alcohol—an essential fatty acid derived from coconut—is combined with glucose to produce lauryl glucoside, a mild, gentle cleanser that doesn’t dry skin or strip it of it’s natural oil. Ideal for use in facial cleansers and hair care products, it’s listed on the Safe Cosmetics Database and the GoodGuide database as being extremely safe. In addition, it’s approved for use in certified organic cosmetics by both the Organic Food Federation and EcoCert. The nice thing about this ingredient is that even though it’s non-irritating and gentle, it has an excellent performance profile in cleansing products, getting skin clean without damaging it. Sodium lauryl glucose carboxylate is a “sodium carboxymethyl ether” of lauryl glucoside, which simply means that it is a derivative of lauryl glucoside that’s a more economical form of the ingredient. Did We Clear It Up? We hope that this explanation clears up the difference for our readers! When you see the word “glucoside” in any ingredient, remember that it comes from glucose (sugar), and that is a much better source than sulfuric acid! As we move towards using INCI names on our products, we feel it's important to inform you about that these long ingredient names mean. Often we're told ‘if you can't pronounce the ingredient, you probably shouldn't use it,' but this is of course an oversimplification. Sodium lauryl glucose carboxylate is a sugar based surfactant used as an emulsifier and stabilizer in creams and lotions. It is produced from naturally occurring raw materials using natural processes and is perfectly safe with no adverse effects. This ingredient is approved for use in certified organic cosmetics by both Organic Food Federation and EcoCert. SODIUM LAURYL GLUCOSE CARBOXYLATE SODIUM LAURYL GLUCOSE CARBOXYLATE is classified as : Cleansing Surfactant COSING REF No: 59276 Chem/IUPAC Name: Sodium carboxymethyl ether of Lauryl Glucoside sodium lauryl glucose carboxylate Rating: GOOD Categories: Cleansing Agents A gentle cleansing agent that may be derived from coconut or made synthetically. Sodium Lauryl Glucose Carboxylate * A surfactant * Also seen as Lauryl Glucose Carboxylate Very little information is available regarding Sodium Lauryl Glucose Carboxylate, although according to TriNature.com, it is a foaming agent that is derived from glucoside from coconut and corn. It is also used as a natural replacement for the ingredient known as sodium laureth sulfate, or SLES. It is seen in cosmetics and personal care products as a surfactant, most often in cleansing formulas such as mild facial washes and special sulfate-free shampoos Functions: Very little information is available regarding Sodium Lauryl Glucose Carboxylate it is a foaming agent that is derived from glucoside from coconut and corn. It is also used as a natural replacement for the ingredient known as sodium laureth sulfate, or SLES. It is seen in cosmetics and personal care products as a surfactant, most often in cleansing formulas such as mild facial washes and special sulfate-free shampoos . Safety Measures/Side Effects: No studies were found that reported any negative side effects regarding the use of Sodium Lauryl Glucose Carboxylate, although it is not reviewed by the Cosmetics Database or EWG. It is considered a milder form or alternative to sodium laureth sulfate and sodium lauryl sulfate. (Sodium lauryl sulfate has been linked to cases of contact dermatitis and other irritation, in part because of its ability change the structure of proteins, while sodium laureth sulfate does not cause this reaction but can still be irritating.) Lauryl Glucoside and Sodium Lauryl Glucose Carboxylate Plant derived mild surfactants made from coconut oil. Sodium lauryl glucose carboxylate is a sugar based surfactant used as an emulsifier and stabilizer, it is produced from naturally occurring raw materials using natural processes and is safe with no adverse effects. Molecular Weight of Sodium Lauryl Glucose Carboxylate: 282.35 g/mol 2.1 Hydrogen Bond Donor Count of Sodium Lauryl Glucose Carboxylate: 1 Hydrogen Bond Acceptor Count of Sodium Lauryl Glucose Carboxylate: 4 Rotatable Bond Count of Sodium Lauryl Glucose Carboxylate: 13 Exact Mass of Sodium Lauryl Glucose Carboxylate: 282.180704 g/mol 2.1 Monoisotopic Mass of Sodium Lauryl Glucose Carboxylate: 282.180704 g/mol 2.1 Topological Polar Surface Area of Sodium Lauryl Glucose Carboxylate: 69.6 Ų Heavy Atom Count of Sodium Lauryl Glucose Carboxylate: 19 Formal Charge of Sodium Lauryl Glucose Carboxylate: 0 Complexity of Sodium Lauryl Glucose Carboxylate: 200 Isotope Atom Count of Sodium Lauryl Glucose Carboxylate: 0 Defined Atom Stereocenter Count of Sodium Lauryl Glucose Carboxylate: 0 Undefined Atom Stereocenter Count of Sodium Lauryl Glucose Carboxylate: 1 Defined Bond Stereocenter Count of Sodium Lauryl Glucose Carboxylate: 0 Undefined Bond Stereocenter Count of Sodium Lauryl Glucose Carboxylate: 0 Covalently-Bonded Unit Count of Sodium Lauryl Glucose Carboxylate: 2 Compound of Sodium Lauryl Glucose Carboxylate Is Canonicalized?: Yes
SODIUM LAURYL PHOSPHATE
cas no 137-16-6 Sarkosyl; n-lauroylsarcosine, sodium salt; N-Methyl-N-(1-oxododecyl)glycine, sodium salt; Sodium n-Lauriyl Sarcosinate; Natrium-N-lauroylsarkosinat (German); N-Lauroilsarcosinato de sodio (Spanish); N-Lauroylsarcosinate de sodium (French);
SODIUM LAURYL SARCOSINATE
cas no 151-21-3 Dodecyl sodium sulfate; SLS; Sulfuric Acid Monododecyl Ester Sodium Salt; Sodium Dodecanesulfate; Dodecyl Alcohol,Hydrogen Sulfate,Sodium Salt; Akyposal SDS;
SODIUM LAURYL SULFATE
SODIUM LAURYL SULFATE Sodium lauryl sulfate (SLS) or sodium laureth sulfate (SLS), sometimes written sodium laurilsulfate, is a synthetic organic compound with the formula CH3(CH2)11SO4Na. It is an anionic surfactant used in many cleaning and hygiene products. This molecule is an organosulfate and a salt. It consists of a 12-carbon tail attached to a sulfate group, that is, it is the sodium salt of dodecyl hydrogen sulfate, the ester of dodecyl alcohol and sulfuric acid. Its hydrocarbon tail combined with a polar "headgroup" give the compound amphiphilic properties and so make it useful as a detergent.[not verified in body] Also derived as a component of mixtures produced from inexpensive coconut and palm oils, Sodium lauryl sulfate is a common component of many domestic cleaning, personal hygiene and cosmetic, pharmaceutical, and food products, as well as of industrial and commercial cleaning and product formulations. Structure and properties Structure of Sodium lauryl sulfate Sodium lauryl sulfate is in the family of organosulfate compounds,[2] and has the formula, CH3(CH2)11SO4Na. It consists of a 12-carbon tail attached to a sulfate group, that is, it is the sodium salt of a 12-carbon alcohol that has been esterified to sulfuric acid. An alternative description is that it is an alkyl group with a pendant, terminal sulfate group attached. As a result of its hydrocarbon tail, and its anionic "head group", it has amphiphilic properties that allow it to form micelles, and so act as a detergent. Physicochemical properties Bottle of 20% Sodium lauryl sulfate in distilled water for use in the laboratory. The critical micelle concentration (CMC) in pure water at 25 °C is 8.2 mM,[1] and the aggregation number at this concentration is usually considered to be about 62.[3] The micelle ionization fraction (α) is around 0.3 (or 30%). Production of Sodium lauryl sulfate Sodium lauryl sulfate is synthesized by treating lauryl alcohol with sulfur trioxide gas, oleum, or chlorosulfuric acid to produce hydrogen lauryl sulfate.[5] The resulting product is then neutralized through the addition of sodium hydroxide or sodium carbonate.[citation needed] Lauryl alcohol can be used in pure form or may be derived from either coconut or palm kernel oil by hydrolysis (which liberates their fatty acids), followed by hydrogenation.[citation needed] When produced from these sources, commercial samples of these "Sodium lauryl sulfate" products are actually not pure Sodium lauryl sulfate, rather a mixture of various sodium alkyl sulfates with Sodium lauryl sulfate being the main component.[6] For instance, Sodium lauryl sulfate is a component, along with other chain-length amphiphiles, when produced from coconut oil, and is known as sodium coco sulfate (SCS).[7] Sodium lauryl sulfate is available commercially in powder, pellet, and other forms (each differing in rates of dissolution), as well as in aqueous solutions of varying concentrations. Applications of Sodium lauryl sulfate Cleaning and hygiene Sodium lauryl sulfate is mainly used in detergents for laundry with many cleaning applications.[8] It is a highly effective surfactant and is used in any task requiring the removal of oily stains and residues; for example, it is found in higher concentrations with industrial products including engine degreasers, floor cleaners, and car exterior cleaners. In lower concentrations, it is found in hand soap, toothpastes, shampoos, shaving creams, and bubble bath formulations, for its ability to create a foam (lather), for its surfactant properties, and in part for its thickening effect. Food additive of Sodium lauryl sulfate Sodium lauryl sulfate, appearing as its synonym sodium lauryl sulfate (SLS), is considered a generally recognized as safe (GRAS) ingredient for food use according to the USFDA (21 CFR 172.822).[11] It is used as an emulsifying agent and whipping aid.[12] SLS is reported to temporarily diminish perception of sweetness. Laboratory applications of Sodium lauryl sulfate Principal applications of Sodium lauryl sulfate Sodium lauryl sulfate, in science referred to as Sodium lauryl sulfate (Sodium lauryl sulfate), is used in cleaning procedures,[14] and is commonly used as a component for lysing cells during RNA extraction and/or DNA extraction, and for denaturing proteins in preparation for electrophoresis in the Sodium lauryl sulfate-PAGE technique. Denaturation of a protein using Sodium lauryl sulfate In the case of Sodium lauryl sulfate-PAGE, the compound works by disrupting non-covalent bonds in the proteins, and so denaturing them, i.e. causing the protein molecules to lose their native conformations and shapes. By binding to proteins at a ratio of one Sodium lauryl sulfate molecule per 2 amino acid residues, the negatively charged detergent provides all proteins with a similar net negative charge and therefore a similar charge-to-mass ratio.[16] In this way, the difference in mobility of the polypeptide chains in the gel can be attributed solely to their length as opposed to both their native charge and shape.[16][17] It is possible to make separation based on the size of the polypeptide chain to simplify the analysis of protein molecules, this can be achieved by denaturing proteins with the detergent Sodium lauryl sulfate.[18] The association of Sodium lauryl sulfate molecules with protein molecules imparts an associated negative charge to the molecular aggregate formed;[citation needed] this negative charge is significantly greater than the original charge of that protein.[citation needed] The electrostatic repulsion that is created by Sodium lauryl sulfate binding forces proteins into a rod-like shape, thereby eliminating differences in shape as a factor for electrophoretic separation in gels.[citation needed] A dodecyl sulfate molecule has two negative charges at the pH value used for electrophoresis, this will lead the net charge of coated polypeptide chains to be much more negative than uncoated chains.[18] The charge-to-mass ratio is essentially identical for different proteins because Sodium lauryl sulfate coating dominates the charge. Miscellaneous applications of Sodium lauryl sulfate Sodium lauryl sulfate is used in an improved technique for preparing brain tissues for study by optical microscopy. The technique, which has been branded as CLARITY, was the work of Karl Deisseroth and coworkers at Stanford University, and involves infusion of the organ with an acrylamide solution to bind the macromolecules of the organ (proteins, nucleic acids, etc.), followed by thermal polymerization to form a "brain–hydrogel" (a mesh interspersed throughout the tissue to fix the macromolecules and other structures in space), and then by lipid removal using Sodium lauryl sulfate to eliminate light scattering with minimal protein loss, rendering the tissue quasi-transparent.[19][20] Along with sodium dodecylbenzene sulfonate and Triton X-100, aqueous solutions of Sodium lauryl sulfate are popular for dispersing or suspending nanotubes, such as carbon nanotubes. Niche uses of Sodium lauryl sulfate Sodium lauryl sulfate has been proposed as a potentially effective topical microbicide, for intravaginal use, to inhibit and possibly prevent infection by various enveloped and non-enveloped viruses such as the herpes simplex viruses, HIV, and the Semliki Forest virus.[22][23] In gas hydrate formation experiments, Sodium lauryl sulfate is used as a gas hydrate growth promoter.[24][25] [26] Researchers aim for gas hydrate promotions as scale-up of industrial applications of gas hydrates such as desalination process,[27] gas storage, and gas separation technologies.[28] Liquid membranes formed from Sodium lauryl sulfate in water have been demonstrated to work as unusual particle separators.[29] The device acts as a reverse filter, allowing large particles to pass while capturing smaller particles. Toxicology of Sodium lauryl sulfate Carcinogenicity Sodium lauryl sulfate is not carcinogenic when consumed or applied directly, even to amounts and concentrations that exceed amounts used in standard commercial products.[30][31] The earlier review of the Cosmetic Ingredient Review (CIR) program Expert Panel in 1983 reported that Sodium lauryl sulfate (there, abbreviated SLS, for sodium lauryl sulfate) in concentrations up to 2%, in a year-long oral dietary studies in dogs, gave no evidence of tumorigenicity or carcinogenicity, and that no excess chromosomal aberrations or clastogenic effects were observed in rats fed up to 1.13% sodium lauryl sulfate in their diets for 90 days, over those on a control diet.[30]:157, 175 The 2005 review by the same group indicated that further available data lacked any available suggestion that Sodium lauryl sulfate or the related ammonium salt of the same amphiphile could be carcinogenic, stating that "Despite assertions to the contrary on the Internet, the carcinogenicity of these ingredients is only a rumor;" both studies conclude that Sodium lauryl sulfate appears "to be safe in formulations designed for discontinuous, brief use followed by thorough rinsing from the surface of the skin. In products intended for prolonged contact with skin, concentrations should not exceed 1%. Sensitivity of Sodium lauryl sulfate Like all detergents, sodium lauryl sulfate removes oils from the skin, and can cause skin and eye irritation.[citation needed] It has been shown to irritate the skin of the face, with prolonged and constant exposure (more than an hour) in young adults.[32] Sodium lauryl sulfate may worsen skin problems in individuals with chronic skin hypersensitivity, with some people being affected more than others.[33][34][35] Oral concerns of Sodium lauryl sulfate The low cost of Sodium lauryl sulfate,[36] its lack of impact on taste,[36] its potential impact on volatile sulfur compounds (VSCs), which contribute to malodorous breath,[37] and its desirable action as a foaming agent have led to the use of Sodium lauryl sulfate in the formulations of toothpastes.[36] A series of small crossover studies (25-34 patients) have supported the efficacy of SLS in the reduction of VSCs, and its related positive impact on breath malodor, although these studies have been generally noted to reflect technical challenges in the control of study design variables.[37] While primary sources from the group of Irma Rantanen at University of Turku, Finland conclude an impact on dry mouth (xerostomia) from SLS-containing pastes, a 2011 Cochrane review of these studies, and of the more general area, concludes that there "is no strong evidence… that any topical therapy is effective for relieving the symptom of dry mouth."[38] A safety concern has been raised on the basis of several studies regarding the effect of toothpaste Sodium lauryl sulfate on aphthous ulcers, commonly referred to as canker or white sores.[36] A consensus regarding practice (or change in practice) has not appeared as a result of the studies.[39][40] As Lippert notes, of 2013, "very few… marketed toothpastes contain a surfactant other than SLS [Sodium lauryl sulfate]," and leading manufacturers continue to formulate their produce with Sodium lauryl sulfate. Interaction with fluoride Some studies have suggested that SLS in toothpaste may decrease the effectiveness of fluoride at preventing dental caries (cavities). This may be due to SLS interacting with the deposition of fluoride on tooth enamel. Readily pourable, palm-derived, high foaming, anionic surfactant used in the chemical formulating and detergent manufacturing industries. It is a higher foaming variation of Sodium Lauryl Sulfate (SLES). Features of Sodium lauryl sulfate : Free flowing liquid makes it easier to pour. Used in wetting agent formulations, liquid detergents, cleaners, shampoos and laundry detergents. Sodium lauryl sulfate dissolves readily in hard and soft water and provides a consistent foam character. Packaging of Sodium lauryl sulfate : Sodium lauryl sulfate is available in IBCs (1000kg bulk containers) and drums. Safety of Sodium lauryl sulfate : Please consult the SDS on Sodium lauryl sulfate before use. Sodium lauryl sulfate (sodium dodecyl sulphate) is a kind of anionic surfactant, dissolves in the water easily, compatibility with anion and non-ionic, good performances on emulsifying, foaming, osmosis, detergency and de-centrality. Sodium lauryl sulfate Powder Sodium lauryl sulfate Powder is a widely used surfactant often used as a foaming agent in many common products like Bath products, shampoos, foaming powders and mony industrial and commercial cleaners. SaveonCitric offers a highly Active, high quality Sodium lauryl sulfate Powdered Sodium lauryl sulfate. If you are formulating a product like a powdered or tablet cleanser, or blending liquid hard surface or carpet cleaners, try Sodium lauryl sulfate Powder. Check the FIFRa list if you are formulating blends and looking for an accepted surfactant. Sodium lauryl sulfate , synonymously, Sodium lauryl sulfate , or sodium laurilsulfate, is a synthetic organic compound with the formula CH3(CH2)11SO4Na. It is an anionic surfactant used in many cleaning and hygiene products. The sodium salt is of an organosulfate class of organics. It consists of a 12-carbon tail attached to a sulfate group, that is, it is the sodium salt of dodecyl hydrogen sulfate, the ester of dodecyl alcohol and sulfuric acid. Its hydrocarbon tail combined with a polar "headgroup" give the compound amphiphilic properties and so make it useful as a detergent.[not verified in body] Also derived as a component of mixtures produced from inexpensive coconut and palm oils, Sodium lauryl sulfate is a common component of many domestic cleaning, personal hygiene and cosmetic, pharmaceutical, and food products, as well as of industrial and commercial cleaning and product formulations. Sodium lauryl sulfate is a widely used surfactant in cleaning products, cosmetic, and personal care products. Sodium lauryl sulfate 's uses in these products have been thoroughly evaluated and determined to be safe for consumers and the environment. Sodium lauryl sulfate , sodium laurilsulfate or Sodium lauryl sulfate (Sodium lauryl sulfate or NaDS) (C12H25SO4Na) is an anionic surfactant used as an emulsifying cleaning agent in many cleaning and hygiene products. Sodium lauryl sulfate is a highly effective surfactant and is used in any task requiring the removal of oily stains and residues. For example, it is found in higher concentrations with industrial products including engine degreasers, floor cleaners, and car wash soaps. It is used in lower concentrations with toothpastes, shampoos, and shaving foams. It is an important component in bubble bath formulations for its thickening effect and its ability to create a lather. WHAT IS Sodium lauryl sulfate ? Sodium lauryl sulfate , also known as Sodium lauryl sulfate, is a widely used surfactant in cleaning products, cosmetics, and personal care products. The Sodium lauryl sulfate formula is a highly effective anionic surfactant used to remove oily stains and residues. It is found in high concentrations in industrial products, including engine degreasers, floor cleaners, and car wash products, where workplace protections can be implemented to avoid unsafe exposures. Sodium lauryl sulfate is also used in lower concentrations in household and personal care products such as cleaning products, toothpastes, shampoos, and shaving foams. SAFETY Sodium lauryl sulfate has been thoroughly reviewed for its safety by a number of governments. Sodium lauryl sulfate from the requirement of tolerance for residues when used as a component of food contact sanitizing solutions applied to all food contact surfaces in public eating places, dairy-processing equipment, and food-processing equipment and utensils at a maximum level in the end-use concentration of 350 parts per million (ppm). The regulation eliminates the need to establish a maximum permissible level for residues of Sodium lauryl sulfate. The Food and Drug Administration (FDA) includes Sodium lauryl sulfate on its list of multipurpose additives allowed to be directly added to food. Sodium lauryl sulfate and Ammonium Lauryl Sulfate are also approved indirect food additives. For example, both ingredients are permitted to be used as components of coatings. Sodium lauryl sulfate and Ammonium Lauryl Sulfate may be used in cosmetics and personal care products marketed in Europe according to the general provisions of the Cosmetics Directive of the European Union. The Organization of Economic Cooperation and Development, which is an organization of 30-plus developed countries, has reviewed the human and environmental hazards of a category of chemicals that includes Sodium lauryl sulfate. No chronic human health hazards, including carcinogenicity, were identified. The hazard assessment for the category (alkyl sulphates, alkane sulphonates and alpha-olefin sulphonates category) is posted on the OECD website. Sodium lauryl sulfate has also been thoroughly reviewed for human safety by an industry funded, independent panel, which found: There is no evidence of harm from the use of Sodium lauryl sulfate in cosmetic products, where there is intentional, direct contact with the skin. The ingredient was reviewed in 1983 and re-reviewed in 2005 by the Cosmetic Ingredient Review (CIR)1 Expert Panel and found to be safe for use in cosmetic and personal care products. Sodium lauryl sulfate can cause skin irritation in some persons, which is one reason why it is important to follow the label instructions when using a cleaning product. A complete report on Sodium lauryl sulfate is available from CIR. Use: -Detergency: tooth paste, shampoo, cosmetic, detergent, etc. -Construction: plasterboard, additive of concrete, coating, etc. -Pharmaceutical: Medicine, pesticide, etc. -Leather: leather soft agent, wool cleaning agent, etc. -Paper making: penetrant, flocculating agent, deinking agent, etc. -Auxiliaries: textile auxiliaries, plastic auxiliaries, etc. -Fire fighting: oil well fire fighting, fire fighting device, etc. -Mineral choosing: mine flotation, coal water mixture, etc. Overview Sodium lauryl sulfate is one of the ingredients you'll find listed on your shampoo bottle. However, unless you're a chemist, you likely don't know what it is. The chemical is found in many cleaning and beauty products, but it's frequently misunderstood. Urban myths have linked it to cancer, skin irritation, and more. Science may tell a different story. How it works Sodium lauryl sulfate is what's known as a "surfactant." This means it lowers the surface tension between ingredients, which is why it's used as a cleansing and foaming agent. Most concerns about Sodium lauryl sulfate stem from the fact that it can be found in beauty and self-care products as well as in household cleaners. Sodium lauryl sulfate is a surfactant with a similar chemical formula. However, SLES is milder and less irritating than Sodium lauryl sulfate. Where you'll find Sodium lauryl sulfate If you look under your bathroom sink, or on the shelf in your shower, it's very likely you'll find Sodium lauryl sulfate in your home. It's used in a variety of products, including: Grooming products, such as shaving cream, lip balm, hand sanitizer, nail treatments, makeup remover, foundation, facial cleansers, exfoliants, and liquid hand soap Hair products, such as shampoo, conditioner, hair dye, dandruff treatment, and styling gel Dental care products, such as toothpaste, teeth whitening products, and mouthwash Bath products, such as bath oils or salts, body wash, and bubble bath Creams and lotions, such as hand cream, masks, anti-itch creams, hair-removal products, and sunscreen You'll notice that all of these products are topical, or applied directly to the skin or body. Sodium lauryl sulfate is also used as a food additive, usually as an emulsifier or a thickener. It can be found in dried egg products, some marshmallow products, and certain dry beverage bases. Are there dangers? The Food and Drug Administration (FDA) regards Sodium lauryl sulfate as safe as a food additive. Regarding its use in cosmetics and body products, the safety assessment study of Sodium lauryl sulfate , published in 1983 in the International Journal of Toxicology (the most recent assessment), found that it's not harmful if used briefly and rinsed from the skin, as with shampoos and soaps. The report says that products that stay on the skin longer shouldn't exceed 1 percent concentration of Sodium lauryl sulfate. However, the same assessment did suggest some possible, albeit minimal, risk to humans using Sodium lauryl sulfate. For example, some tests found that continuous skin exposure to Sodium lauryl sulfate could cause mild to moderate irritation in animals. Nevertheless, the assessment concluded that Sodium lauryl sulfate is safe in formulations used in cosmetics and personal care products. Because many of these products are designed to be rinsed off after short applications, the risks are minimal. According to most research, Sodium lauryl sulfate is an irritant but not a carcinogen. Studies have shown no link between the use of Sodium lauryl sulfate and increased cancer risk. According to a 2015 study, Sodium lauryl sulfate is safe for use in household cleaning products. About 1/3 of HIV positive mothers transmit the virus to their newborns, and 1/2 of these infections occur during breastfeeding. Sodium lauryl sulfate (SLS), an anionic surfactant, is a common ingredient of cosmetic and personal care products. Sodium lauryl sulfate is "readily biodegradable" with low toxicity and "is of no concern with respect to human health". Up to 1 g of Sodium lauryl sulfate/kg is the maximum safe dose for children. Alkyl sulfates, including Sodium lauryl sulfate, are microbicidal against HIV types 1 and 2, herpes simplex virus type 2 (HSV-2), human papillomaviruses and chlamydia. /The study/ hypothesizes that Sodium lauryl sulfate treatment of milk will inactivate HIV-1 without significant harm to its nutritional value and protective functions and may define a treatment of choice for breastwas at 37 degrees C for 10 min. Sodium lauryl sulfate-PAGE and Lowry were used to analyze protein content. Antibody content and function was studied by rocket immunoelectrophoresis (RIE), immunoturbodimentric (ITM) quantitation and ELISA. The creamatocrit was also analyzed. HIV-1 infectivity was measured by MAGI assay. Sodium lauryl sulfate removal was by Detergent-OutN (Geno Technology, Inc.). Sodium lauryl sulfate quantitation is by methylene blue-chloroform method. Inactivation of HIV-1 with Sodium lauryl sulfate occurs at or above 0.025%. In milk samples, 1% and 0.1% Sodium lauryl sulfate reduced HSV-2 infectivity. At least 90% of Sodium lauryl sulfate can be efficiently removed with Detergent-OutN, with protein recovery of 80%-100%. Gross protein species are conserved as indicated by PAGE analyses. Fat and energy content of Sodium lauryl sulfate-treated breast milk remains unchanged. 0.1% Sodium lauryl sulfate can be removed from human milk without altering the creamatocrit. ELISA of serum IgG (rubella) proved it remains functional in the presence of Sodium lauryl sulfate and after its removal. sIgA, IgG and IgM in breast milk are conserved after Sodium lauryl sulfate-treatment when measured by RIE and ITM. CONCLUSIONS: Sodium lauryl sulfate (0.025%) can inactivate HIV-1 in vitro and HSV-2 in breast milk. Sodium lauryl sulfate can be efficiently removed from milk samples. Sodium lauryl sulfate treatment of milk does not significantly alter protein content. Antibody function in serum and levels in breast milk are maintained after treatment and removal of Sodium lauryl sulfate. 0.1% Sodium lauryl sulfate does not alter fat concentration in milk and energy content is conserved. Sodium lauryl sulfate or related compounds may be used to prevent breast milk transmission of HIV-1. A broad-spectrum vaginal microbicide must be effective against a variety of sexually transmitted disease pathogens and be minimally toxic to the cell types found within the vaginal epithelium, including vaginal keratinocytes. /The study/ assessed the sensitivity of primary human vaginal keratinocytes to potential topical vaginal microbicides nonoxynol-9 (N-9), C31G, and Sodium lauryl sulfate (SLS). Direct immunofluorescence and fluorescence-activated cell sorting analyses demonstrated that primary vaginal keratinocytes expressed epithelial cell-specific keratin proteins. Experiments that compared vaginal keratinocyte sensitivity to each agent during a continuous, 48-hr exposure demonstrated that primary vaginal keratinocytes were almost five times more sensitive to N-9 than to either C31G or Sodium lauryl sulfate. To evaluate the effect of multiple microbicide exposures on cell viability, primary vaginal keratinocytes were exposed to N-9, C31G, or Sodium lauryl sulfate three times during a 78-hr period. In these experiments, cells were considerably more sensitive to C31G than to N-9 or Sodium lauryl sulfate at lower concentrations within the range tested. When agent concentrations were chosen to result in an endpoint of 25% viability after three daily exposures, each exposure decreased cell viability at the same constant rate. When time-dependent sensitivity during a continuous 48-hr exposure was examined, exposure to C31G for 18 hr resulted in losses in cell viability not caused by either N-9 or Sodium lauryl sulfate until at least 24 to 48 hr. Cumulatively, these results reveal important variations in time- and concentration-dependent sensitivity to N-9, C31G, or Sodium lauryl sulfate within populations of primary human vaginal keratinocytes cultured in vitro. These investigations represent initial steps toward both in vitro modeling of the vaginal microenvironment and studies of factors that impact the in vivo efficacy of vaginal topical microbicides. Sodium lauryl sulfate (SLS) is an anionic detergent that can form complexes with protein through hydrophobic interactions. Studies have reported that the hydrodynamic functions of protein-Sodium lauryl sulfate complexes are governed by the length of their polypeptide chains. Thus, Sodium lauryl sulfate-based electrophoretic techniques can separate protein molecules based on their molecular weights. Additionally, Sodium lauryl sulfate can solubilize cell membranes and can extract membrane-bound proteins. Analytical procedures are described for determining residues of Sodium lauryl sulfate in whole blood from guinea pigs. Methods are based on hydrolysis & analysis by electron-capture gas-chromatography. Sodium lauryl sulfate Electrophoresis Sodium lauryl sulfate electrophoresis was the next logical step after disk electrophoresis. While the latter discriminates macromolecules on the basis of both size and surface charge, Sodium lauryl sulfate electrophoresis fractionates polypeptide chains essentially on the basis of their size. It is therefore a simple, yet powerful and reliable method for molecular mass (Mr) determination. In 1967, it was first reported that electrophoretic migration in Sodium lauryl sulfate is proportional to the effective molecular radius and thus to the Mr of the polypeptide chain. This result means that Sodium lauryl sulfate must bind to proteins and cancel out differences in molecular charge, so that all components then migrate solely according to size. Surprisingly large amounts of Sodium lauryl sulfate appear to be bound (an average of 1.4 g Sodium lauryl sulfate per gram of protein), which means that the number of Sodium lauryl sulfate molecules bound is of the order of half the number of amino acid residues in a polypeptide chain. This amount of highly charged surfactant molecules is sufficient to overwhelm effectively the intrinsic charges of the polymer coil, so that their net charge per unit mass becomes approximately constant. If migration in Sodium lauryl sulfate (and disulfide reducing agents, such as 2-mercaptoethanol, in the denaturing step, for a proper unfolding of the proteins) is proportional only to molecular mass, then, in addition to canceling out of charge differences, Sodium lauryl sulfate also equalizes molecular shape differences as well (e.g., globular versus rod-shaped molecules). This seems to be the case for protein–Sodium lauryl sulfate mixed micelles: these complexes can be assumed to behave as ellipsoids of constant minor axis (∼1.8 nm) and with the major axis proportional to the length in amino acids (i.e., to molecular mass) of the protein. The rod length for the 1.4 g Sodium lauryl sulfate/g protein complex is of the order of 0.074 nm per amino acid residue. Sodium lauryl sulfate Sodium lauryl sulfate (SLS), also known as lauryl sulfate, is an ionic detergent that is useful for the rapid disruption of biological membranes. It is a key component of many reagents used to purify nucleic acids because of its abilities to quickly disrupt the tissue architecture and to inhibit both RNase and deoxyribonuclease (DNase) activity. Sodium lauryl sulfate is usually prepared as either a 10% or a 20% (w/v) stock solution and is used most often at a working concentration of 0.1% to 0.5%. The performance of this detergent can be affected significantly by its purity. Sodium lauryl sulfate is easily precipitable in the presence of potassium salts and generally is not added to guanidinium buffers, as it has very low solubility in high-salt, chaotropic solutions. Two classes of proteins show anomalous behavior in Sodium lauryl sulfate electrophoresis: glycoproteins (because their hydrophilic oligosaccharide units prevent hydrophobic binding of Sodium lauryl sulfate micelles) and strongly basic proteins (e.g., histones) (because of electrostatic binding of Sodium lauryl sulfate micelles through their sulfate groups). The first can be partially alleviated by using Tris–borate buffers at alkaline pH, which will increase the net negative charge on the glycoprotein, thus producing migration rates well correlated with molecular size. Migration of histones can be improved by using pore gradient gels and allowing the polypeptide chains to approach the pore limit.
SODIUM LAURYL SULFATE (POWDER)
Sodium Lauryl Sulfate Powder Sodium lauryl sulfate powder (SLS) or sodium laureth sulfate (SLS), sometimes written sodium laurilsulfate, is a synthetic organic compound with the formula CH3(CH2)11SO4Na. It is an anionic surfactant used in many cleaning and hygiene products. This molecule is an organosulfate and a salt. It consists of a 12-carbon tail attached to a sulfate group, that is, it is the sodium salt of dodecyl hydrogen sulfate, the ester of dodecyl alcohol and sulfuric acid. Its hydrocarbon tail combined with a polar "headgroup" give the compound amphiphilic properties and so make it useful as a detergent.[not verified in body] Also derived as a component of mixtures produced from inexpensive coconut and palm oils, Sodium lauryl sulfate powder is a common component of many domestic cleaning, personal hygiene and cosmetic, pharmaceutical, and food products, as well as of industrial and commercial cleaning and product formulations. Structure and properties Structure of Sodium lauryl sulfate powder Sodium lauryl sulfate powder is in the family of organosulfate compounds,[2] and has the formula, CH3(CH2)11SO4Na. It consists of a 12-carbon tail attached to a sulfate group, that is, it is the sodium salt of a 12-carbon alcohol that has been esterified to sulfuric acid. An alternative description is that it is an alkyl group with a pendant, terminal sulfate group attached. As a result of its hydrocarbon tail, and its anionic "head group", it has amphiphilic properties that allow it to form micelles, and so act as a detergent. Physicochemical properties Bottle of 20% Sodium lauryl sulfate powder in distilled water for use in the laboratory. The critical micelle concentration (CMC) in pure water at 25 °C is 8.2 mM,[1] and the aggregation number at this concentration is usually considered to be about 62.[3] The micelle ionization fraction (α) is around 0.3 (or 30%). Production of Sodium lauryl sulfate powder Sodium lauryl sulfate powder is synthesized by treating lauryl alcohol with sulfur trioxide gas, oleum, or chlorosulfuric acid to produce hydrogen lauryl sulfate.[5] The resulting product is then neutralized through the addition of sodium hydroxide or sodium carbonate.[citation needed] Lauryl alcohol can be used in pure form or may be derived from either coconut or palm kernel oil by hydrolysis (which liberates their fatty acids), followed by hydrogenation.[citation needed] When produced from these sources, commercial samples of these "Sodium lauryl sulfate powder" products are actually not pure Sodium lauryl sulfate powder, rather a mixture of various sodium alkyl sulfates with Sodium lauryl sulfate powder being the main component.[6] For instance, Sodium lauryl sulfate powder is a component, along with other chain-length amphiphiles, when produced from coconut oil, and is known as sodium coco sulfate (SCS).[7] Sodium lauryl sulfate powder is available commercially in powder, pellet, and other forms (each differing in rates of dissolution), as well as in aqueous solutions of varying concentrations. Applications of Sodium lauryl sulfate powder Cleaning and hygiene Sodium lauryl sulfate powder is mainly used in detergents for laundry with many cleaning applications.[8] It is a highly effective surfactant and is used in any task requiring the removal of oily stains and residues; for example, it is found in higher concentrations with industrial products including engine degreasers, floor cleaners, and car exterior cleaners. In lower concentrations, it is found in hand soap, toothpastes, shampoos, shaving creams, and bubble bath formulations, for its ability to create a foam (lather), for its surfactant properties, and in part for its thickening effect. Food additive of Sodium lauryl sulfate powder Sodium lauryl sulfate powder, appearing as its synonym Sodium lauryl sulfate powder (SLS), is considered a generally recognized as safe (GRAS) ingredient for food use according to the USFDA (21 CFR 172.822).[11] It is used as an emulsifying agent and whipping aid.[12] SLS is reported to temporarily diminish perception of sweetness. Laboratory applications of Sodium lauryl sulfate powder Principal applications of Sodium lauryl sulfate powder Sodium lauryl sulfate powder, in science referred to as Sodium lauryl sulfate powder (Sodium lauryl sulfate powder), is used in cleaning procedures,[14] and is commonly used as a component for lysing cells during RNA extraction and/or DNA extraction, and for denaturing proteins in preparation for electrophoresis in the Sodium lauryl sulfate powder-PAGE technique. Denaturation of a protein using Sodium lauryl sulfate powder In the case of Sodium lauryl sulfate powder-PAGE, the compound works by disrupting non-covalent bonds in the proteins, and so denaturing them, i.e. causing the protein molecules to lose their native conformations and shapes. By binding to proteins at a ratio of one Sodium lauryl sulfate powder molecule per 2 amino acid residues, the negatively charged detergent provides all proteins with a similar net negative charge and therefore a similar charge-to-mass ratio.[16] In this way, the difference in mobility of the polypeptide chains in the gel can be attributed solely to their length as opposed to both their native charge and shape.[16][17] It is possible to make separation based on the size of the polypeptide chain to simplify the analysis of protein molecules, this can be achieved by denaturing proteins with the detergent Sodium lauryl sulfate powder.[18] The association of Sodium lauryl sulfate powder molecules with protein molecules imparts an associated negative charge to the molecular aggregate formed;[citation needed] this negative charge is significantly greater than the original charge of that protein.[citation needed] The electrostatic repulsion that is created by Sodium lauryl sulfate powder binding forces proteins into a rod-like shape, thereby eliminating differences in shape as a factor for electrophoretic separation in gels.[citation needed] A dodecyl sulfate molecule has two negative charges at the pH value used for electrophoresis, this will lead the net charge of coated polypeptide chains to be much more negative than uncoated chains.[18] The charge-to-mass ratio is essentially identical for different proteins because Sodium lauryl sulfate powder coating dominates the charge. Miscellaneous applications of Sodium lauryl sulfate powder Sodium lauryl sulfate powder is used in an improved technique for preparing brain tissues for study by optical microscopy. The technique, which has been branded as CLARITY, was the work of Karl Deisseroth and coworkers at Stanford University, and involves infusion of the organ with an acrylamide solution to bind the macromolecules of the organ (proteins, nucleic acids, etc.), followed by thermal polymerization to form a "brain–hydrogel" (a mesh interspersed throughout the tissue to fix the macromolecules and other structures in space), and then by lipid removal using Sodium lauryl sulfate powder to eliminate light scattering with minimal protein loss, rendering the tissue quasi-transparent.[19][20] Along with sodium dodecylbenzene sulfonate and Triton X-100, aqueous solutions of Sodium lauryl sulfate powder are popular for dispersing or suspending nanotubes, such as carbon nanotubes. Niche uses of Sodium lauryl sulfate powder Sodium lauryl sulfate powder has been proposed as a potentially effective topical microbicide, for intravaginal use, to inhibit and possibly prevent infection by various enveloped and non-enveloped viruses such as the herpes simplex viruses, HIV, and the Semliki Forest virus.[22][23] In gas hydrate formation experiments, Sodium lauryl sulfate powder is used as a gas hydrate growth promoter.[24][25] [26] Researchers aim for gas hydrate promotions as scale-up of industrial applications of gas hydrates such as desalination process,[27] gas storage, and gas separation technologies.[28] Liquid membranes formed from Sodium lauryl sulfate powder in water have been demonstrated to work as unusual particle separators.[29] The device acts as a reverse filter, allowing large particles to pass while capturing smaller particles. Toxicology of Sodium lauryl sulfate powder Carcinogenicity Sodium lauryl sulfate powder is not carcinogenic when consumed or applied directly, even to amounts and concentrations that exceed amounts used in standard commercial products.[30][31] The earlier review of the Cosmetic Ingredient Review (CIR) program Expert Panel in 1983 reported that Sodium lauryl sulfate powder (there, abbreviated SLS, for Sodium lauryl sulfate powder) in concentrations up to 2%, in a year-long oral dietary studies in dogs, gave no evidence of tumorigenicity or carcinogenicity, and that no excess chromosomal aberrations or clastogenic effects were observed in rats fed up to 1.13% Sodium lauryl sulfate powder in their diets for 90 days, over those on a control diet.[30]:157, 175 The 2005 review by the same group indicated that further available data lacked any available suggestion that Sodium lauryl sulfate powder or the related ammonium salt of the same amphiphile could be carcinogenic, stating that "Despite assertions to the contrary on the Internet, the carcinogenicity of these ingredients is only a rumor;" both studies conclude that Sodium lauryl sulfate powder appears "to be safe in formulations designed for discontinuous, brief use followed by thorough rinsing from the surface of the skin. In products intended for prolonged contact with skin, concentrations should not exceed 1%. Sensitivity of Sodium lauryl sulfate powder Like all detergents, Sodium lauryl sulfate powder removes oils from the skin, and can cause skin and eye irritation.[citation needed] It has been shown to irritate the skin of the face, with prolonged and constant exposure (more than an hour) in young adults.[32] Sodium lauryl sulfate powder may worsen skin problems in individuals with chronic skin hypersensitivity, with some people being affected more than others.[33][34][35] Oral concerns of Sodium lauryl sulfate powder The low cost of Sodium lauryl sulfate powder,[36] its lack of impact on taste,[36] its potential impact on volatile sulfur compounds (VSCs), which contribute to malodorous breath,[37] and its desirable action as a foaming agent have led to the use of Sodium lauryl sulfate powder in the formulations of toothpastes.[36] A series of small crossover studies (25-34 patients) have supported the efficacy of SLS in the reduction of VSCs, and its related positive impact on breath malodor, although these studies have been generally noted to reflect technical challenges in the control of study design variables.[37] While primary sources from the group of Irma Rantanen at University of Turku, Finland conclude an impact on dry mouth (xerostomia) from SLS-containing pastes, a 2011 Cochrane review of these studies, and of the more general area, concludes that there "is no strong evidence… that any topical therapy is effective for relieving the symptom of dry mouth."[38] A safety concern has been raised on the basis of several studies regarding the effect of toothpaste Sodium lauryl sulfate powder on aphthous ulcers, commonly referred to as canker or white sores.[36] A consensus regarding practice (or change in practice) has not appeared as a result of the studies.[39][40] As Lippert notes, of 2013, "very few… marketed toothpastes contain a surfactant other than SLS [Sodium lauryl sulfate powder]," and leading manufacturers continue to formulate their produce with Sodium lauryl sulfate powder. Interaction with fluoride Some studies have suggested that SLS in toothpaste may decrease the effectiveness of fluoride at preventing dental caries (cavities). This may be due to SLS interacting with the deposition of fluoride on tooth enamel. Readily pourable, palm-derived, high foaming, anionic surfactant used in the chemical formulating and detergent manufacturing industries. It is a higher foaming variation of Sodium lauryl sulfate powder (SLES). Features of Sodium lauryl sulfate powder : Free flowing liquid makes it easier to pour. Used in wetting agent formulations, liquid detergents, cleaners, shampoos and laundry detergents. Sodium lauryl sulfate powder dissolves readily in hard and soft water and provides a consistent foam character. Packaging of Sodium lauryl sulfate powder : Sodium lauryl sulfate powder is available in IBCs (1000kg bulk containers) and drums. Safety of Sodium lauryl sulfate powder : Please consult the SDS on Sodium lauryl sulfate powder before use. Sodium lauryl sulfate powder (sodium dodecyl sulphate) is a kind of anionic surfactant, dissolves in the water easily, compatibility with anion and non-ionic, good performances on emulsifying, foaming, osmosis, detergency and de-centrality. Sodium lauryl sulfate powder Powder Sodium lauryl sulfate powder Powder is a widely used surfactant often used as a foaming agent in many common products like Bath products, shampoos, foaming powders and mony industrial and commercial cleaners. SaveonCitric offers a highly Active, high quality Sodium lauryl sulfate powder Powdered Sodium lauryl sulfate powder. If you are formulating a product like a powdered or tablet cleanser, or blending liquid hard surface or carpet cleaners, try Sodium lauryl sulfate powder Powder. Check the FIFRa list if you are formulating blends and looking for an accepted surfactant. Sodium lauryl sulfate powder , synonymously, Sodium lauryl sulfate powder , or sodium laurilsulfate, is a synthetic organic compound with the formula CH3(CH2)11SO4Na. It is an anionic surfactant used in many cleaning and hygiene products. The sodium salt is of an organosulfate class of organics. It consists of a 12-carbon tail attached to a sulfate group, that is, it is the sodium salt of dodecyl hydrogen sulfate, the ester of dodecyl alcohol and sulfuric acid. Its hydrocarbon tail combined with a polar "headgroup" give the compound amphiphilic properties and so make it useful as a detergent.[not verified in body] Also derived as a component of mixtures produced from inexpensive coconut and palm oils, Sodium lauryl sulfate powder is a common component of many domestic cleaning, personal hygiene and cosmetic, pharmaceutical, and food products, as well as of industrial and commercial cleaning and product formulations. Sodium lauryl sulfate powder is a widely used surfactant in cleaning products, cosmetic, and personal care products. Sodium lauryl sulfate powder 's uses in these products have been thoroughly evaluated and determined to be safe for consumers and the environment. Sodium lauryl sulfate powder , sodium laurilsulfate or Sodium lauryl sulfate powder (Sodium lauryl sulfate powder or NaDS) (C12H25SO4Na) is an anionic surfactant used as an emulsifying cleaning agent in many cleaning and hygiene products. Sodium lauryl sulfate powder is a highly effective surfactant and is used in any task requiring the removal of oily stains and residues. For example, it is found in higher concentrations with industrial products including engine degreasers, floor cleaners, and car wash soaps. It is used in lower concentrations with toothpastes, shampoos, and shaving foams. It is an important component in bubble bath formulations for its thickening effect and its ability to create a lather. WHAT IS Sodium lauryl sulfate powder ? Sodium lauryl sulfate powder , also known as Sodium lauryl sulfate powder, is a widely used surfactant in cleaning products, cosmetics, and personal care products. The Sodium lauryl sulfate powder formula is a highly effective anionic surfactant used to remove oily stains and residues. It is found in high concentrations in industrial products, including engine degreasers, floor cleaners, and car wash products, where workplace protections can be implemented to avoid unsafe exposures. Sodium lauryl sulfate powder is also used in lower concentrations in household and personal care products such as cleaning products, toothpastes, shampoos, and shaving foams. SAFETY Sodium lauryl sulfate powder has been thoroughly reviewed for its safety by a number of governments. Sodium lauryl sulfate powder from the requirement of tolerance for residues when used as a component of food contact sanitizing solutions applied to all food contact surfaces in public eating places, dairy-processing equipment, and food-processing equipment and utensils at a maximum level in the end-use concentration of 350 parts per million (ppm). The regulation eliminates the need to establish a maximum permissible level for residues of Sodium lauryl sulfate powder. The Food and Drug Administration (FDA) includes Sodium lauryl sulfate powder on its list of multipurpose additives allowed to be directly added to food. Sodium lauryl sulfate powder and Ammonium Lauryl Sulfate are also approved indirect food additives. For example, both ingredients are permitted to be used as components of coatings. Sodium lauryl sulfate powder and Ammonium Lauryl Sulfate may be used in cosmetics and personal care products marketed in Europe according to the general provisions of the Cosmetics Directive of the European Union. The Organization of Economic Cooperation and Development, which is an organization of 30-plus developed countries, has reviewed the human and environmental hazards of a category of chemicals that includes Sodium lauryl sulfate powder. No chronic human health hazards, including carcinogenicity, were identified. The hazard assessment for the category (alkyl sulphates, alkane sulphonates and alpha-olefin sulphonates category) is posted on the OECD website. Sodium lauryl sulfate powder has also been thoroughly reviewed for human safety by an industry funded, independent panel, which found: There is no evidence of harm from the use of Sodium lauryl sulfate powder in cosmetic products, where there is intentional, direct contact with the skin. The ingredient was reviewed in 1983 and re-reviewed in 2005 by the Cosmetic Ingredient Review (CIR)1 Expert Panel and found to be safe for use in cosmetic and personal care products. Sodium lauryl sulfate powder can cause skin irritation in some persons, which is one reason why it is important to follow the label instructions when using a cleaning product. A complete report on Sodium lauryl sulfate powder is available from CIR. Use: -Detergency: tooth paste, shampoo, cosmetic, detergent, etc. -Construction: plasterboard, additive of concrete, coating, etc. -Pharmaceutical: Medicine, pesticide, etc. -Leather: leather soft agent, wool cleaning agent, etc. -Paper making: penetrant, flocculating agent, deinking agent, etc. -Auxiliaries: textile auxiliaries, plastic auxiliaries, etc. -Fire fighting: oil well fire fighting, fire fighting device, etc. -Mineral choosing: mine flotation, coal water mixture, etc. Overview Sodium lauryl sulfate powder is one of the ingredients you'll find listed on your shampoo bottle. However, unless you're a chemist, you likely don't know what it is. The chemical is found in many cleaning and beauty products, but it's frequently misunderstood. Urban myths have linked it to cancer, skin irritation, and more. Science may tell a different story. How it works Sodium lauryl sulfate powder is what's known as a "surfactant." This means it lowers the surface tension between ingredients, which is why it's used as a cleansing and foaming agent. Most concerns about Sodium lauryl sulfate powder stem from the fact that it can be found in beauty and self-care products as well as in household cleaners. Sodium lauryl sulfate powder is a surfactant with a similar chemical formula. However, SLES is milder and less irritating than Sodium lauryl sulfate powder. Where you'll find Sodium lauryl sulfate powder If you look under your bathroom sink, or on the shelf in your shower, it's very likely you'll find Sodium lauryl sulfate powder in your home. It's used in a variety of products, including: Grooming products, such as shaving cream, lip balm, hand sanitizer, nail treatments, makeup remover, foundation, facial cleansers, exfoliants, and liquid hand soap Hair products, such as shampoo, conditioner, hair dye, dandruff treatment, and styling gel Dental care products, such as toothpaste, teeth whitening products, and mouthwash Bath products, such as bath oils or salts, body wash, and bubble bath Creams and lotions, such as hand cream, masks, anti-itch creams, hair-removal products, and sunscreen You'll notice that all of these products are topical, or applied directly to the skin or body. Sodium lauryl sulfate powder is also used as a food additive, usually as an emulsifier or a thickener. It can be found in dried egg products, some marshmallow products, and certain dry beverage bases. Are there dangers? The Food and Drug Administration (FDA) regards Sodium lauryl sulfate powder as safe as a food additive. Regarding its use in cosmetics and body products, the safety assessment study of Sodium lauryl sulfate powder , published in 1983 in the International Journal of Toxicology (the most recent assessment), found that it's not harmful if used briefly and rinsed from the skin, as with shampoos and soaps. The report says that products that stay on the skin longer shouldn't exceed 1 percent concentration of Sodium lauryl sulfate powder. However, the same assessment did suggest some possible, albeit minimal, risk to humans using Sodium lauryl sulfate powder. For example, some tests found that continuous skin exposure to Sodium lauryl sulfate powder could cause mild to moderate irritation in animals. Nevertheless, the assessment concluded that Sodium lauryl sulfate powder is safe in formulations used in cosmetics and personal care products. Because many of these products are designed to be rinsed off after short applications, the risks are minimal. According to most research, Sodium lauryl sulfate powder is an irritant but not a carcinogen. Studies have shown no link between the use of Sodium lauryl sulfate powder and increased cancer risk. According to a 2015 study, Sodium lauryl sulfate powder is safe for use in household cleaning products. About 1/3 of HIV positive mothers transmit the virus to their newborns, and 1/2 of these infections occur during breastfeeding. Sodium lauryl sulfate powder (SLS), an anionic surfactant, is a common ingredient of cosmetic and personal care products. Sodium lauryl sulfate powder is "readily biodegradable" with low toxicity and "is of no concern with respect to human health". Up to 1 g of Sodium lauryl sulfate powder/kg is the maximum safe dose for children. Alkyl sulfates, including Sodium lauryl sulfate powder, are microbicidal against HIV types 1 and 2, herpes simplex virus type 2 (HSV-2), human papillomaviruses and chlamydia. /The study/ hypothesizes that Sodium lauryl sulfate powder treatment of milk will inactivate HIV-1 without significant harm to its nutritional value and protective functions and may define a treatment of choice for breastwas at 37 degrees C for 10 min. Sodium lauryl sulfate powder-PAGE and Lowry were used to analyze protein content. Antibody content and function was studied by rocket immunoelectrophoresis (RIE), immunoturbodimentric (ITM) quantitation and ELISA. The creamatocrit was also analyzed. HIV-1 infectivity was measured by MAGI assay. Sodium lauryl sulfate powder removal was by Detergent-OutN (Geno Technology, Inc.). Sodium lauryl sulfate powder quantitation is by methylene blue-chloroform method. Inactivation of HIV-1 with Sodium lauryl sulfate powder occurs at or above 0.025%. In milk samples, 1% and 0.1% Sodium lauryl sulfate powder reduced HSV-2 infectivity. At least 90% of Sodium lauryl sulfate powder can be efficiently removed with Detergent-OutN, with protein recovery of 80%-100%. Gross protein species are conserved as indicated by PAGE analyses. Fat and energy content of Sodium lauryl sulfate powder-treated breast milk remains unchanged. 0.1% Sodium lauryl sulfate powder can be removed from human milk without altering the creamatocrit. ELISA of serum IgG (rubella) proved it remains functional in the presence of Sodium lauryl sulfate powder and after its removal. sIgA, IgG and IgM in breast milk are conserved after Sodium lauryl sulfate powder-treatment when measured by RIE and ITM. CONCLUSIONS: Sodium lauryl sulfate powder (0.025%) can inactivate HIV-1 in vitro and HSV-2 in breast milk. Sodium lauryl sulfate powder can be efficiently removed from milk samples. Sodium lauryl sulfate powder treatment of milk does not significantly alter protein content. Antibody function in serum and levels in breast milk are maintained after treatment and removal of Sodium lauryl sulfate powder. 0.1% Sodium lauryl sulfate powder does not alter fat concentration in milk and energy content is conserved. Sodium lauryl sulfate powder or related compounds may be used to prevent breast milk transmission of HIV-1. A broad-spectrum vaginal microbicide must be effective against a variety of sexually transmitted disease pathogens and be minimally toxic to the cell types found within the vaginal epithelium, including vaginal keratinocytes. /The study/ assessed the sensitivity of primary human vaginal keratinocytes to potential topical vaginal microbicides nonoxynol-9 (N-9), C31G, and Sodium lauryl sulfate powder (SLS). Direct immunofluorescence and fluorescence-activated cell sorting analyses demonstrated that primary vaginal keratinocytes expressed epithelial cell-specific keratin proteins. Experiments that compared vaginal keratinocyte sensitivity to each agent during a continuous, 48-hr exposure demonstrated that primary vaginal keratinocytes were almost five times more sensitive to N-9 than to either C31G or Sodium lauryl sulfate powder. To evaluate the effect of multiple microbicide exposures on cell viability, primary vaginal keratinocytes were exposed to N-9, C31G, or Sodium lauryl sulfate powder three times during a 78-hr period. In these experiments, cells were considerably more sensitive to C31G than to N-9 or Sodium lauryl sulfate powder at lower concentrations within the range tested. When agent concentrations were chosen to result in an endpoint of 25% viability after three daily exposures, each exposure decreased cell viability at the same constant rate. When time-dependent sensitivity during a continuous 48-hr exposure was examined, exposure to C31G for 18 hr resulted in losses in cell viability not caused by either N-9 or Sodium lauryl sulfate powder until at least 24 to 48 hr. Cumulatively, these results reveal important variations in time- and concentration-dependent sensitivity to N-9, C31G, or Sodium lauryl sulfate powder within populations of primary human vaginal keratinocytes cultured in vitro. These investigations represent initial steps toward both in vitro modeling of the vaginal microenvironment and studies of factors that impact the in vivo efficacy of vaginal topical microbicides. Sodium lauryl sulfate powder (SLS) is an anionic detergent that can form complexes with protein through hydrophobic interactions. Studies have reported that the hydrodynamic functions of protein-Sodium lauryl sulfate powder complexes are governed by the length of their polypeptide chains. Thus, Sodium lauryl sulfate powder-based electrophoretic techniques can separate protein molecules based on their molecular weights. Additionally, Sodium lauryl sulfate powder can solubilize cell membranes and can extract membrane-bound proteins. Analytical procedures are described for determining residues of Sodium lauryl sulfate powder in whole blood from guinea pigs. Methods are based on hydrolysis & analysis by electron-capture gas-chromatography. Sodium lauryl sulfate powder Electrophoresis Sodium lauryl sulfate powder electrophoresis was the next logical step after disk electrophoresis. While the latter discriminates macromolecules on the basis of both size and surface charge, Sodium lauryl sulfate powder electrophoresis fractionates polypeptide chains essentially on the basis of their size. It is therefore a simple, yet powerful and reliable method for molecular mass (Mr) determination. In 1967, it was first reported that electrophoretic migration in Sodium lauryl sulfate powder is proportional to the effective molecular radius and thus to the Mr of the polypeptide chain. This result means that Sodium lauryl sulfate powder must bind to proteins and cancel out differences in molecular charge, so that all components then migrate solely according to size. Surprisingly large amounts of Sodium lauryl sulfate powder appear to be bound (an average of 1.4 g Sodium lauryl sulfate powder per gram of protein), which means that the number of Sodium lauryl sulfate powder molecules bound is of the order of half the number of amino acid residues in a polypeptide chain. This amount of highly charged surfactant molecules is sufficient to overwhelm effectively the intrinsic charges of the polymer coil, so that their net charge per unit mass becomes approximately constant. If migration in Sodium lauryl sulfate powder (and disulfide reducing agents, such as 2-mercaptoethanol, in the denaturing step, for a proper unfolding of the proteins) is proportional only to molecular mass, then, in addition to canceling out of charge differences, Sodium lauryl sulfate powder also equalizes molecular shape differences as well (e.g., globular versus rod-shaped molecules). This seems to be the case for protein–Sodium lauryl sulfate powder mixed micelles: these complexes can be assumed to behave as ellipsoids of constant minor axis (∼1.8 nm) and with the major axis proportional to the length in amino acids (i.e., to molecular mass) of the protein. The rod length for the 1.4 g Sodium lauryl sulfate powder/g protein complex is of the order of 0.074 nm per amino acid residue. Sodium lauryl sulfate powder Sodium lauryl sulfate powder (SLS), also known as lauryl sulfate, is an ionic detergent that is useful for the rapid disruption of biological membranes. It is a key component of many reagents used to purify nucleic acids because of its abilities to quickly disrupt the tissue architecture and to inhibit both RNase and deoxyribonuclease (DNase) activity. Sodium lauryl sulfate powder is usually prepared as either a 10% or a 20% (w/v) stock solution and is used most often at a working concentration of 0.1% to 0.5%. The performance of this detergent can be affected significantly by its purity. Sodium lauryl sulfate powder is easily precipitable in the presence of potassium salts and generally is not added to guanidinium buffers, as it has very low solubility in high-salt, chaotropic solutions. Two classes of proteins show anomalous behavior in Sodium lauryl sulfate powder electrophoresis: glycoproteins (because their hydrophilic oligosaccharide units prevent hydrophobic binding of Sodium lauryl sulfate powder micelles) and strongly basic proteins (e.g., histones) (because of electrostatic binding of Sodium lauryl sulfate powder micelles through their sulfate groups). The first can be partially alleviated by using Tris–borate buffers at alkaline pH, which will increase the net negative charge on the glycoprotein, thus producing migration rates well correlated with molecular size. Migration of histones can be improved by using pore gradient gels and allowing the polypeptide chains to approach the pore limit.
SODIUM LAURYL SULFOACETATE
cas no 8061-51-6 Sodium base spent sulfite liquor; Llignosol; Sodium lignosulfonate; Desulfonated spent pulping liquor; Sodium lignosulfonate; Sodium lignosulfite; Sodium polignate; Llignosulfonic acids sodium salt; Sulfonated lignin sodium salt;
SODIUM LINOLEATE
SODIUM MAGNESIUM FLUOROSILICATE Nom INCI : SODIUM MAGNESIUM FLUOROSILICATE Ses fonctions (INCI) Agent Abrasif : Enlève les matières présentes en surface du corps, aide à nettoyer les dents et améliore la brillance. Agent Absorbant : Absorbe l'eau (ou l'huile) sous forme dissoute ou en fines particules Opacifiant : Réduit la transparence ou la translucidité des cosmétiques Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques
SODIUM MAGNESIUM FLUOROSILICATE
SODIUM MAGNESIUM SILICATE N° CAS : 101659-01-2 Nom INCI : SODIUM MAGNESIUM SILICATE N° EINECS/ELINCS : 258-476-2 Compatible Bio (Référentiel COSMOS) Ses fonctions (INCI) Agent fixant : Permet la cohésion de différents ingrédients cosmétiques Agent de foisonnement : Réduit la densité apparente des cosmétiques Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques
SODIUM MAGNESIUM SILICATE
SODIUM MALATE N° CAS : 58214-38-3 Nom INCI : SODIUM MALATE Nom chimique : Butanedioic acid, hydroxy-, monosodium salt N° EINECS/ELINCS : 261-169-6 Ses fonctions (INCI) Humectant : Maintient la teneur en eau d'un cosmétique dans son emballage et sur la peau Agent d'entretien de la peau : Maintient la peau en bon état
SODIUM MALATE
SYNONYMS Dinatriumdisulfit; Disulfito de disodio; Disulfite de disodium; Disodium disulfite; Disodium Salt Pyrosulfurous Acid; Disulfurous acid, disodium salt; Pyrosulfurous acid, disodium salt; Sodium Metabisulfite; Sodium disulfite; Sodium Pyrosulfite; CAS NO. 7681-57-4
SODIUM METABORATE
SODIUM METAPERIODATE N° CAS : 7790-28-5 - Periodate de sodium Nom INCI : SODIUM METAPERIODATE
SODIUM METABORATE
CAS number: 98536584
EC number: 2318916
Molecular formula: NaBO2
Molecular weight: 65.80

APPLICATION AND BENEFITS
Adhesives:
Sodium Metaborate’s high alkalinity and the crosslinking reaction of borate anions with polyhydroxy groups makes it an excellent choice for starch and dextrinbased adhesives.
The adhesives Sodium Metaborate helps to produce are essential for use in corrugated boxes, paper bags, laminated paper boards, carton and case sealing, gummed tape, and tube winding.

Photography:
Sodium Metaborate is also a component of photographic developers and replenishers.
Sodium Metaborates principal function is as a buffering agent, used to tightly control the pH of the solutions.
As such, Sodium Metaborate produces highquality finegrain blackandwhite developers and helps to ensurethe correct color balance in color developers.

Bleaching agent:
Textiles, such as cotton, are bleached with hydrogen peroxide solutions.
These solutions can be stabilized by using sodium metaborate.
Sodium Metaborate also neutralizes the acidic oxidation byproducts that form during bleaching.
And, textile manufacturers can control textile sizing by incorporating sodium metaborateproduced starch adhesive material within the thread and binding all the fibers together to increase the thread’s tensile strength.

Cleaners:
As an ingredient in hardsurface cleaners, sodium metaborate helps to remove oil, grease, rust, scale, and other particulates from metal or glass surfaces.
The borate imparts alkaline conditions that enhance the product’s cleaning action.
Sodium Metaborate can also be incorporated into liquid laundry detergents for pH control, enzyme stabilization, and its builder properties.

Many proprietary watertreatment chemicals also include sodium metaborate to control pH and inhibit corrosion.
Such chemicals are used on heating systems and cooling towers as protection against corrosion.
In automotive and industrial fluids, sodium metaborate can be used for anticorrosion and reaction with acidic degradation products.
Borates are also being developed as an alkaline agent in several enhanced oil recover (EOR) processes, such as alkalipolymer and alkalisurfactantpolymer (ASP) flooding.
Tertiary oil recovery from boratebased ASP core floods is comparable to that obtained with similar formulations that contain conventional alkalis and exhibit no injectivity problems in core flood trials.

Sodium Metaborate is stable at ordinary temperatures.
However, if exposed to the atmosphere for extended periods, it picks up carbon dioxide from the air and forms sodium carbonate and borax.
Sodium Metaborate 4 mol will convert to 8 mol when exposed to a humid atmosphere.

Sodium Metaborate 4 mol crystalline salt begins to lose water at about 194°F (90°C).
The anhydrous salt fuses to a clear glass at 1770°F (966°C).
Some vaporization occurs above 2246°F (1230°C).

Sodium Metaborate 8 mol crystalline salt begins to lose water at about 128°F (53.5°C).
The anhydrous salt fuses to a clear glass at 1770°F (966°C), and some vaporization occurs above 2246°F (1230°C).
Aqueous solutions of sodium metaborate 4 mol and 8 mol show a moderate increase in pH with increasing concentrations.

Sodium Metaborate is the sodium salt of Metaborate.
Sodium Metaborate is used in the manufacturing of borosilicate glasses.
Sodium Metaborate is also a component of herbicides and antifreeze.
Sodium Metaborate can also be used as an oil additive with antiwear properties.

Agricultural Uses:
Herbicide
Insecticide
Fungicide
Nematocid

Sodium Metaborate electroreduction in the alkaline system can act as a novel desulphurization process of coal water slurry.
Sodium Metaborate also has role in hydrolysis of sodium borohydride to minimize the water utilization.
Sodium Metaborate can also act as a novel alkali in alkali/surfactant/polymer flooding.
Sodium Metaborate is also useful in the thermochemical production of sodium borohydride, which is a safe and practical hydrogen storage material for onboard hydrogen production.
Also available commercially as octahydrate and tetrahydrate.

Sodium Metaborate tetrahydrate is used In textile industry
Sodium Metaborate is used as additives, process aid and flame retardant.
Sodium Metaborate Octahydrate is generally immediately available in most volumes.
High purity, submicron and nanopowder forms may be considered.

Sources/Uses:
Sodium Metaborate is used in;
-cleansersdetergents
-adhesives
-photographic solutions

Also Sodium Metaborate is used as:
-a fire retardant in sodium chlorate
-a defoliant
-a textile finishing agent
-a sequestrant;

Preparation:
Sodium Metaborate is prepared by the fusion of sodium carbonate and boron oxide B2O3 or borax Na2B4O7.
Another way to create the compound is by the fusion of borax with sodium hydroxide at 700 °C:
B2O3 + 2 NaOH → 2 NaBO2 + H2O
The boiling point of sodium metaborate (1434 °C) is lower than that of boron oxide (1860 °C) and borax (1575 °C) In fact, while the metaborate boils without change of composition, borax gives off a vapor of sodium metaborate with a small excess of sodium oxide Na2O

Electrochemical Conversion to Borax:
Electrolysis of a concentrated solution of 20% NaBO2·4H2O with an anion exchange membrane and inert anode (such as gold, palladium, or borondoped diamond) converts the metaborate anion to tetraborate B4O2−7, and the sodium salt of the later (borax) precipitates as a white powder

Reduction to Sodium Borohydride:
Sodium Metaborate is also a byproduct of hydrolysis of sodium borohydride NaBH4, a proposed hydrogen storage material for hydrogenfueled vehicles that is safer (stable in dry air) and more efficient on a weight basis than most other alternatives.
The reaction is:
NaBH4 + 2 H2O → NaBO2 + 4 H2 and requires a catalyst.

To be economical, that approach would require a cheap and efficient method to recycle the metaborate to the borohydride.
Several methods have been studied, such as the reaction with various reducing agents at high temperatures and pressure, or with magnesium hydride MgH2 by ball milling at room temperature, followed by extraction of the NaBH4 with isopropylamine.

NaBO2 + 2 MgH2 → NaBH4 + 2 MgO
Another alternative that has been considered is the electrolytic reduction of a concentrated sodium metaborate solution, namely
BO2−2 + 6 H2O + 8 e− → BH−4 + 8 HO−
However, this method is not efficient since it competes with the reduction of hydroxide, 4 HO−→ 2 H2O + O2 + 4 e−

Conversion to Sodium Alkoxides:
Anhydrous sodium metaborate refluxed with methanol yields the corresponding sodium methoxyborate:
Na+[BO2]− + 4 CH3OH → Na+[B(OCH3)4]− + 2 H2O
The analogous reaction with ethanol yields the ethoxyborate.

Metabolism/Metabolites:
Boric acid, sodium salt and borates are not metabolized, neither do they accumulate in the body except for low deposit in bone.
No organic boron compounds have been reported as metabolites.

Essential Buffering Agent
Used in the preparation of starch and dextrin adhesives, this product provides increased viscosity, quicker tack, and better fluidity.
In textile processing, sodium metaborate helps to stabilize hydrogen peroxide solutions and neutralizes acidic oxidation byproducts.

Hydrates and Solubility:
The following hydrates crystallize from solutions of the proper composition in various temperature ranges:

tetrahydrate NaBO2·4H2O from −6 to 53.6 °C
dihydrate NaBO2·2H2O from 53.6 °C to 105 °C
hemihydrate NaBO2·0.5H2O from 105 °C to the boiling point.

Early reports of a monohydrate NaBO2·H2O have not been confirmed.
The anhydrous salt can be prepared from the tetraborate by heating to 270 °C in vacuum

Tetrahydrate: Used as
an insecticide
fungicide
nematocide
herbicide (noncrop land, cotton production, and under asphalt)

Sodium Metaborate is a colorless solid chemical compound of sodium, boron, and oxygen.
Sodium Metaborate is an inorganic sodium salt having metaborate as the counterion.
Sodium Metaborate is an inorganic sodium salt and a member of borate salts.

Sodium Metaborate is a colorless solid chemical compound of sodium, boron, and oxygen with formula NaBO2.
Sodium Metaborate is a colorless solid chemical compound of sodium, boron, and oxygen with formula NaBO₂.
The formula can be written also as Na₂O·B₂O₃ to highlight the relation to the main oxides of sodium and boron.

Sodium Metaborate, a derivative of the borax compound, has a wide range of industrial applications.
Recently, Sodium Metaborate is used as a source of boron in the production of sodium borohydride (NaBH4), which is a medium for hydrogen storage.
In the present study, sodium metaborate tetrahydrate (SMT, NaB(OH)(4)center dot 2H(2)O) was produced by the reaction of borax (B) with the sodium hydroxide (SH) solution under ultrasonic irradiation.

The effect of the reaction parameters (amount of water. temperature, particle size, and time) on the production of sodium metaborate tetrahydrate was investigated in the present study.
Sodium Metaborate was shown that the reaction parameters (amount of water, temperature, and time) played a significant role in the synthesis of sodium metaborate tetrahydrate.
In addition, the concentration of characteristic BO group in the reaction solution was quantitatively determined by Fourier Transform Infrared Spectroscopy (FTIR).

The optimum condition for the production process included 26% water by weight, borax particles of size 250+150 mu m and irradiation time of 60 min at 80 degrees C.
Sodium Metaborate is An alkaline salt with excellent buffering properties.
Sodium Metaborate Can also be used in the production of adhesives due to the high degree of alkalinity and the crosslinking reaction of borate anions with polyhydroxy groups.
The formula can be written also as Na2O·B2O3 to highlight the relation to the main oxides of sodium and boron

Uses of Sodium Metaborate:
Sodium Metaborate is used in the manufacturing of borosilicate glasses.
Sodium Metaborate is also a component of herbicides and antifreeze products.

Solid anhydrous sodium metaborate crystallizes in the hexagonal space group.
Sodium Metaborate actually contains the trimeric anion [B3O6]3−.
The six oxygen atoms are evenly divided into two distinct structural sites, with different B–O bond lengths (about 128 and 143 pm, respectively)

Sodium Metaborate, a derivative of the borax compound, has a wide range of industrial applications.
Sodium Metaborate is used as a source of boron in the production of sodium borohydride (NaBH 4 ), which is a medium for hydrogen storage.

PHYSICAL PROPERTIES OF SODIUM METABORATE:
Molecular Weight: 65.80
Exact Mass: 65.9889037
Monoisotopic Mass: 65.9889037
Topological Polar Surface Area: 40.1 Ų
Physical Description: Liquid
Color: White
Form: powder/White hexagonal crystals
Odor: Odorless
Boiling Point: 1434 °C
Melting Point: 966 °C
Solubility: In water, 36 g/100 g
Density: 2.46 g/cu cm
Stability/Shelf Life: Stable on storage
pH: Solution is strongly alkaline when dissolved in water
Enthalpy of fusion: 36.2 kJ/mol at 966 °C

CHEMICAL PROPERTIES OF SODIUM METABORATE:
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 0
Heavy Atom Count: 4
Formal Charge: 0
Complexity: 13.5
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
CovalentlyBonded Unit Count: 2
Compound Is Canonicalized: Yes
Corrosivity: NONCORROSIVE TO FERROUS METALS

APPLICATIONS OF SODIUM METABORATE:
-Adhesives
-Photography
-Bleaching agent
-Cleaners
-Paper industry
-Plating
-Cleaning agents
-Industry derived products
-Manufacture of heat resistant products

STORAGE OF SODIUM METABORATE:
Sodium Metaborate should be stored at room temperature.
Sodium Metaborate should be stored in a moisturefree environment.
Sodium Metaborate should be stored in dry place.

Sodium Metaborate is often used as a component of most photographic developers and replenishers.
Typically, Sodium Metaborate acts as a buffering agent in order to control acidity levels.
In addition to such applications, the compound is commonly utilized as an adhesive as well.
A very specific effect of the compound can be seen in the preparation of starch and dextrin adhesives due to its high degree of alkalinity.

An interchain linkage will produce an adhesive that has powerful viscosity, along with quicker tack and much more fluid properties.
All of these qualities make this adhesive essential in a wide variety of different industries.
Sodium Metaborate can be commonly used in corrugated boxes, most paper bags, various paper boards, and gummed tape.
Such versatile applications make Sodium Metaborate a desired compound for most household items and applications

Sodium Metaborate, a derivative of the borax compound, has a wide range of industrial applications.
Recently, Sodium Metaborate is used as a source of boron in the production of sodium borohydride (NaBH₄), which is a medium for hydrogen storage.
In the present study, sodium metaborate tetrahydrate (SMT, NaB(OH)₄·2H₂O) was produced by the reaction of borax (B) with the sodium hydroxide (SH) solution under ultrasonic irradiation.

The effect of the reaction parameters (amount of water, temperature, particle size, and time) on the production of sodium metaborate tetrahydrate was investigated in the present study.
Sodium Metaborate was shown that the reaction parameters (amount of water, temperature, and time) played a significant role in the synthesis of sodium metaborate tetrahydrate.
In addition, the concentration of characteristic B–O group in the reaction solution was quantitatively determined by Fourier Transform Infrared Spectroscopy (FTIR).
The optimum condition for the production process included 26% water by weight, borax particles of size −250+150μm and irradiation time of 60min at 80°C

SYNONYMS:
disodium borate, heptahydrate
disodium borate, monohydrate
Komex
monosodium metaborate
sodium borate
sodium borate (NaBO2)
sodium diborate
sodium meta borate
sodium metaborate
sodium tetraborat
Kodalk
sodium;oxido(oxo)borane
Boric acid, monosodium salt
UNIIZ6Q395A23R
Sodium(1+), (metaboratoO)
Borosoap
Z6Q395A23R
Boric acid (HBO2), sodium salt (1:1)
Sodium Metaborate, anhydrous
Sodium borate (NaBO2)
SODIUMMETABORATE
NaBO2
EC 2318916
SODIUM METABORATE GR
DTXSID2034386
CHEBI:75227
AKOS024426998
SODIUM METAPERIODATE
SYNONYMS Metso Beads, Silicic acid, disodium salt; Sodium-m-Silicate; Orthosil; Disodium metasilicate; Disodium Monosilicate; Waterglass; Disodium trioxosilicate CAS NO. 6834-92-0 (Anhydrous), 10213-79-3 (Pentahydrate), 13517-24-3 (Nonahydrate)
SODIUM METASILICATE ANHYDRATE
cas no 10213-79-3 Metso Beads, Silicic acid, disodium salt; Sodium-m-Silicate; Orthosil; Disodium metasilicate; Disodium Monosilicate; Waterglass; Disodium trioxosilicate;
SODIUM METHYL ISETHIONATE
SYNONYMS Methyl 4-hydroxybenzoate, sodium salt; Sodium 4-(methoxycarbonyl)phenolate; Natrium-4-(methoxycarbonyl)phenolat; 4-(metoxicarbonil)fenolato de sodio; 4-(méthoxycarbonyl)phénolate de sodium; Methyl paraben sodium salt; Sodium methyl 4-hydroxybenzoate; methyl-4-oxide-benzoate, sodium salt; Methyl p-hydroxybenzoate, sodium salt; CAS NO. 5026-62-0
SODIUM METHYL P-HYDROXYBENZOATE (SODIUM METHYLPARABEN)
cas no 5026-62-0 Methyl 4-hydroxybenzoate, sodium salt; Sodium 4-(methoxycarbonyl)phenolate; Natrium-4-(methoxycarbonyl)phenolat; 4-(metoxicarbonil)fenolato de sodio; 4-(méthoxycarbonyl)phénolate de sodium; Methyl paraben sodium salt; Sodium methyl 4-hydroxybenzoate; methyl-4-oxide-benzoate, sodium salt; Methyl p-hydroxybenzoate, sodium salt;
SODIUM METHYLPARABENE
Chemical name: Sodium Methyl p-Hydroxybenzoate. Sodium methylparaben (sodium methyl para-hydroxybenzoate) is a compound with formula Na(CH3(C6H4COO)O). Sodium methylparaben is the sodium salt of methylparaben. Sodium methylparaben is a food additive with the E number E219 which is used as a preservative. IUPAC name: Sodium 4-(methoxycarbonyl)phenolate Use: Sodium methyl paraben is widely used in food and pharmaceutical and textile industry for its antiseptic property. Sodium methyl paraben is also can be used in other industries such as cosmetics, feed and so on. Use: Preservative, Cosmetics, Feed, Pharmaceutical, Antimicrobial, Antifungal, Antibacterial, Soft Drink, Alcohol Beverage, Beverage Powder, Fruit Juice, Puddings, Sauces, Baking Food, Sauage, Food Colors, Milk, Wine, Flavoring Agent. Sodium methyl p-hydroxybenzoate; Methylparaben sodium salt; E219 CAS Number: 5026-62-0 Sodium methylparaben is a sodium salt of methylparaben, which is used as an additive for food preservation. Sodium methylparaben is prepared by adding p-hydroxybenzoate to sodium hydroxide and after reaction is finished, standing for crystallization, centrifugally filtering and finally carrying out vacuum drying. Sodium methylparaben is a constituent of cloudberry, yellow passion fruit, white wine, and botrytis wine. Sodium methylparaben is extensively used to produce foods, beverages, pharmaceuticals, cosmetics, agriculture/ animal feed, flavoring agents, and medicines as an antimicrobial agent. Sodium methylparaben has a faint characteristic odor or is odorless and has a slight burnt taste. INCI designation Sodium Methylparaben. Product properties Appearance: White powder Chemical and physical data pH: 9.5- 10.5 Water content: max. 5.0 % Assay by non aqueous titration: 99 - 102 % Uses Sodium Methylparaben is a broad spectrum antimicrobial agent designed for preservation of a wide range of cosmetics, toiletries pharmaceuticals. Sodium Methylparaben is suitable to preserve both rinse- off and leave-on formulations. Sodium Methylparaben is effective against bacteria, molds and yeast. The recommended use level of Sodium Methylparaben to preserve most product types is normally in the range of 0.1- 0.3 % based on the total weight of the finished product. The Paraben esters have many advantages as preservatives,like broad spectrum antimicrobial activity, effective at low use concentrations, compatible with a wide range of cosmetic ingredients, colourless, odourless, well documented toxicological and dermatological acceptability based on human experience (used in cosmetics, food and pharmaceuticals since 1930ies), p-Hydroxybenzoic Acid and a number of its esters occur naturally in a variety of plants and animals, stable and effective over a wide pH- range, etc. The Sodium Parabens, like Sodium Methylparaben have several additional advantages: Sodium Methylparaben is highly soluble in cold water for ease of addition. No heating stage required for incorporation, thus saving energy and plant occupancy. Increased antimicrobial activity at alkaline pH. Applications Sodium Methylparaben is designed for preservation of a wide range of cosmetics and toiletries. Sodium Methyl paraben is suitable to preserve both rinse- off and leave- on formulations. Formulations which are prone to bacteria contamination an additional antibacterial preservative, like DMDMH might be necessary to add as Sodium Methylparaben provides a higher efficacy against fungi than against bacteria. Solubility Water up to 33 % Incorporation Sodium Methylparaben is highly soluble in water and so easily incorporated into cosmetic formulations. It is important to note that, whilst the aqueous solubility in alkaline solution is high, if the pH of the formulated product is acidic the sodium salt reverts to the ester and the low solubility is regained. pH stability Sodium Methyl paraben remains fully stable over a wide pH range from 3.0- 11.0. Aqueous solutions of Sodium Methylparaben are not long- term stable at alkaline pH. Temperature stability The recommended maximum handling temperature is 80°C. Microbial activity Sodium Methylparaben has a broad spectrum of activity which includes the following common spoilage organisms. Microorganisms MIC level (%) Bacteria Pseudomonas aeruginosa 0.228 Staphylococcus aureus 0.17 Microorganisms MIC level (%) Yeasts Candida albicans 0.114 Molds Aspergillus niger 0.114 Regulatory Status Sodium Methylparaben can be used up to a maximum concentration of 0.4 % in cosmetic products, no further restrictions. Storage instructions Sodium Methyl paraben is stable in sealed original containers. Further information on handling, storage and dispatch is given in the EC safety data sheet. Sodium Methyl paraben is a broad spectrum antimicrobial agent designed for preservation of a wide range of cosmetics, toiletries, and topical pharmaceuticals. It is suitable to preserve both rinse-off and leave-on formulations. This product is highly soluble in cold water for ease of addition. Sodium Methylparaben is designed for preservation of a wide range of cosmetics and toiletries. Sodium Methylparaben is suitable to preserve both rinse- off and leave- on formulations. Sodium Methylparaben is a broad spectrum antimicrobial agent designed forpreservation of a wide range of cosmetics, toiletries pharmaceuticals. Sodium Methylparaben is suitable to preserve both rinse- off and leave- onformulations.Sodium Methylparaben is effective against bacteria, molds and yeast. The recommended use level of Sodium Methylparaben to preserve most product types is normally in the range of 0.1 - 0.3 % based on the total weight of the finished product. The Paraben esters have many advantages as preservatives, like broad spectrumantimicrobial activity, effective at low use concentrations, compatible with awide range of cosmetic ingredients, colourless, odourless, well documentedtoxicological and dermatological acceptability based on human experience (usedin cosmetics, food and pharmaceuticals since 1930ies), p-Hydroxybenzoic Acidand a number of its esters occur naturally in a variety of plants and animals,stable and effective over a wide pH- range, etc. The Sodium Parabens, like Sodium Methylparaben have several additional advantages: Sodium Methyl paraben is highly soluble in cold water for ease of addition. No heating stage required for incorporation, thus saving energy and plant occupancy. Increased antimicrobial activity at alkaline pH. Sodium Methylparaben is a highly water-soluble short-chain paraben in sodium salt form. The major benefit offered by the sodium salts is their high solubility in cold water, thereby enabling the introduction of parabens without heating or pre-dissolving in solvents. Benefits High solubility in cold water Broad spectrum of activity against bacteria and fungi Low order of toxicity Effectiveness at low concentrations Stability over a broad pH-range Water-soluble Biodegradability at environmental concentrations Global acceptance in personal care applications Sodium Methylparaben Market: Segmentation Overview Based on end-user, the sodium methylparaben market is divided into food & beverages, cosmetics, and pharmaceuticals. Sodium methyl paraben is used as a food preservative in the food & beverage industry. Sodium Methyl paraben is used to inhibit the Clostridium botulinum bacteria, which causes fatal botulism. Sodium Methyl paraben is used in baked foods, creams & pastes, jams & jellies, syrups, dairy products, and beverages. Sodium Methyl paraben is employed as a preservative in cosmetics with other parabens. Sodium methyl paraben is utilized in makeup, hair care products, moisturizers & lotions, shaving products, and toothpastes. Sodium Methyl paraben is also used to protect pharmaceutical products from microorganism. The cosmetics and food & beverages segments are expected to account for large shares of the market. In terms of value, the cosmetics segment is anticipated to expand at a considerable pace during the forecast period. In terms of application, the global sodium methylparaben market is segmented into antimicrobial preservatives, anti-fungal agents, and others. The antimicrobial preservative segment is projected to expand at a steady pace during the forecasted period. Based on product type, the sodium methylparaben market is bifurcated into powder and liquid. Sodium Methylparaben. Sodium Methyl paraben by Clariant is a water-soluble preservative. Sodium Methyl paraben is a short-chain paraben in sodium salt form. Sodium Methylparaben offers a broad spectrum of activity against bacteria & fungi and stability over a broad pH-range. Sodium Methylparaben exhibits effectiveness at low concentrations. Sodium Methylparaben shows high solubility in cold water, low order of toxicity and good biodegradability at environmental concentrations. Sodium Methylparaben is used in all kinds of personal care products.
SODIUM MOLYBDATE







Sodium molybdate, Na2MoO4, is useful as a source of molybdenum. This white, crystalline salt is often found as the dihydrate, Na2MoO4·2H2O.

CAS Number
10102-40-6 (dihydrate)
7631-95-0


EC / List no.: 600-158-6
CAS no.: 10102-40-6

Molybdate (MoO42-), sodium, hydrate (1:2:2), (T-4)-

IUPAC names
disodium dioxido(dioxo)molybdenum dihydrate
disodium;dioxido(dioxo)molybdenum;dihydrate
Molybdate (MoO42-), sodium, hydrate (1:2:2), (T-4)-
Molybdenan sodný dihydrát
Natriummolybdat-Dihydrat
sodium molibdate 2h2o
Sodium Molybdate
sodium molybdate
sodium molybdate dhydrate
Sodium molybdate dihydrate
sodium molybdate dihydrate

disodium molibdate
Molybdate (MoO4(2-)), disodium, dihydrate, (T-4)
Sodium Molybdate
Sodium molybdate dihydrate







EC / List no.: 231-551-7
CAS no.: 7631-95-0
Disodium molybdate
CAS names: Molybdate (MoO42-), sodium (1:2), (T-4)-


IUPAC names
Dinatriumdioxido(dioxo)molybdon
Dinatriummolybdat dihydrat
Disodium dioxido (dioxo)molybdate
disodium dioxido(dioxo)molybdenum
disodium dioxido(dioxo)molybdenum dihydrate
disodium dioxido-dioxomolybdenum
disodium dioxomolybdenumbis(olate)
Disodium Molybdate
Disodium tetraoxomolybdate
disodium tetraoxomolybdate dihydrate
disodium;dioxido(dioxo)molybdenum
SODIUM MOLYBDATE
Sodium molybdate dihydrate
Sodium molybdate(VI) dihydrate


NaMo
Sodium Molybdate
Sodium Molybdate Anhydrous
Sodium Molybdate Crystalline (SMC)
Sodium Molybdate Dihydrate
SoMo





WHAT IS SODIUM MOLYBDATE?
There are two main forms of Sodium Molybdate.
Sodium Molybdate, Dihydrate is a crystalline powder.
It loses its water of crystallization at 100 degrees Celsius.
It is known to be less toxic than the other corresponding compounds of group 6B elements in the periodic table.
Sodium Molybdate, Dihydrate is used in the manufacturing of inorganic and organic pigments, as a corrosion inhibitor, as a bath additive for finishing metals finishing, as a reagent for alkaloids, and as an essential micronutrient for plants and animals.


Sodium Molybdate, Anhydrous is a small, lustrous, crystalline plate.
It has the melting point of 687 degrees Celsius and a density of 3.28 (18C).
It is soluble in water and also noncombustible.
It can be used for reagent in analytical chemistry, paint pigment, production of molybdated toners and lakes, metal finishing, brightening agent for zinc plating, corrosion inhibitor, catalyst in dye and pigment production, additive for fertilizers and feeds, and micronutrient.


SODIUM MOLIBDATE is a Plant Nutrient that is directly involved in the metabolic functions of nitrogen in the plant.
Sodium molybdate helps with the uptake of nitrogen, ensuring efficient nitrogen-fixing for these plants, and allowing nitrogen to be synthesized into ammonia and essential amino acids.

Sodium molybdate is a source of molybdenum oxide, and this chemical has a variety of useful industrial, commercial, and agricultural purposes

SODIUM MOLIBDATE is a crystalline powder of 100% sodium molybdate, which may be used either as a seeddressing or foliar spray to combat molybdenum deficiency in agricultural crops.


Sodium Molybdate (Sodium Molybdate Dihydrate) is widely used in manufacturing, including agricultural fertilizers, pigments, catalysts, fire retardants, corrosion inhibitors, as well as water treatment.




CROP RATE OF APPLICATION REMARKS

LUCERN: 125 – 250 g/ha
Seed treatment simultaneously with inoculation.

GRASS/CLOVER PASTURES: 155 g/ha
Foliar spray onto young regrowth after cutting.

TOMATOES: 250 g/ha Molybdenum deficiency occurs generally in the Transvaal Lowveld, especially on acid soils.
Apply to the planting furrow just before transplanting, or as a foliar spray.

MAIZE: 60 g/1,25 ℓ water
Place 100 kg seed in a drum with watertight lid.
Add the solution and turn the drum over for 15 to 20 minutes by rolling or by turning on an axle by means of a handle.
The seed may be treated any time before planting.

CRUCIFEROUS CROPS: 100 – 250 g/ha
Spray the young plants with a solution of water.

CUCURBITS: 2 g/1 ℓ water
Let the seed soak overnight in a 0,2% solution and plant directly afterwards.

SUNFLOWER: 25 g/25 g seed A solution of the trace element should be applied uniformly to the seed.
50 g/100 ℓ water Apply to the seedling as a full cover foliar spray.




Why Sodium Molybdate Is Used In Agriculture Industry

In recent times, the agriculture sector is used the best chemical compounds for fertilizer.
One of the popular chemicals for fertilizer application is sodium molybdate.
The fertilizer uses this chemical easily soluble in water and soaks into the soil that reduces the runoff.
It helps to reduce the waste chemical compound, which can harm the environment.
Sodium Molybdate is mostly used as an important micronutrient for animals and plants, additive for metals finishing, and much more.

Overview of sodium molybdate

It is available in different forms such as Sodium Molybdate and Dihydrate, which is a crystalline powder.
This chemical is lower toxic when compared to other compounds of group 6B parts in the table.
It is mostly used in organic and inorganic pigment manufacturing.
Anhydrous is a small crystalline plate that has a 687 degrees Celsius melting point.
This chemical is easily soluble in water.
It is mostly used for reagents in paint pigment, molybdated toner production, brightening agent for zinc plating, paint pigment, and much more.


Benefits of using Sodium Molybdate

Nowadays, Sodium Molybdate is used in different sectors such as printing, manufacturing, metalwork, agriculture, and others due to its benefits.
Over one million pounds of this chemical fertilizer are used every year. Followings are some common benefits of using this mineral.

The molybdate contains lots of elements in the highest oxidation state. It helps to the high solubility of chemical compounds in the water.
Sodium Molybdate is beneficial for fertilizer application in the agriculture sector.
Sodium Molybdate is used as a delivery vessel for important micronutrients in the plant.
It is the main reason for using this chemical compound for fertilizer in agriculture.

Farmers mostly use sodium molybdate that provides important micronutrients.
Sodium Molybdate helps to drive the function of the plant effectively. The efficiency of the plant is not only by the smaller amount required to make an impact on the plant.
It can administer the chemical in absorbing water-based substances quickly.

Sodium Molybdate is mostly used by people who focus on leguminous plants such as peanut, peas, lentils, alfalfa, and much more.
Sodium Molybdate aids with the nitrogen intake and assures effective nitrogen-fixing for some plants.
This chemical lets to fix atmospheric nitrogen available in the surrounding by the bacteria.
It converts the nitrogen to synthesize into the amino acid, ammonia, and others in the plant.


Agricultural Additive For Fertilizer
Sodium molybdate is widely used as an agricultural additive on farms.
It’s an ideal choice for fertilizer applications.
This is because the basic chemistry of molybdate compounds like sodium molybdate include molybdenum oxide at its highest oxidation state.

This means that Sodium molybdate is highly-soluble in water.
This means that fertilizers using sodium molybdate easily combine and mix with water and soak into soil, delivering molybdenum oxide and other valuable micronutrients into the roots and minimizing runoff, which wastes chemical compounds and can have negative environmental consequences.

Sodium molybdate is particularly popular among farmers who primarily focus on legumes like lentils, beans, alfalfa, and peanuts.
Sodium molybdate helps with the uptake of nitrogen, ensuring efficient nitrogen-fixing for these plants, and allowing nitrogen to be synthesized into ammonia and essential amino acids.


Hydroponic Farming & Agriculture
Similarly to traditional soil-based fertilizer applications, sodium molybdate can be used in hydroponic farming, which uses inert substrates as the growing medium instead of soil.
Mineral nutrient solutions are delivered directly to the plants using water, so highly-soluble nutrients and fertilizers – such as sodium molybdate – are very desirable for these purposes.


Corrosion Inhibitor
Sodium molybdate is commonly used as a metal corrosion inhibitor for iron and steel, and is commonly found in water treatment products like chiller systems, where bimetallic design and construction can raise the risk of metal corrosion.

This additive is primarily used in closed-loop systems, and is regarded to be far superior to other corrosion inhibitors like sodium nitrate.
At concentrations of just 50 to 100 ppm, sodium molybdate offers superior performance compared to 800+ ppm concentrations of sodium nitrate.


Sodium Molybdate is used in water treatment, including industrial water treatment due to its low toxicity.
The advantage of Sodium Molybdate in water treatment is that it is effective in low dosages, which maintains low conductivity of water and prevents corrosion by reducing galvanic corrosion potentials.

Sodium Molybdate is also used for metal surface treatment, including galvanizing and polishing.



Nutritional Supplement
Some people may choose to supplement their diets with sodium molybdate.
These products can be found on their own, but molybdenum is typically found in multivitamins and complex vitamins.
Typical doses for dietary supplements range from about 50 mcg to 500 mcg (micrograms) of sodium molybdate.

Most people do not need an additional source of molybdenum, as this micronutrient is present in a wide variety of foods, such as legumes, yogurt, potatoes, whole-grain bread, beef liver, spinach, corn, cheese, tuna, and more.

However, in individuals who may have an improper diet or who wish to ensure they get adequate micronutrients, sodium molybdate is a good option.
Cases of toxicity due to excessive intake of molybdenum are rare, and usually only occur due to exposure in the mining and metalworking industries, so supplementing with sodium molybdate is typically harmless.




Molybdenum importance for appropriate plant functioning and growth is inconsistent by the most of the plants in respect to the total quantity that is obligatory for them.
Molybdenum is a micronutrient that is directly involved in the metabolic functions of nitrogen in the plant.
The transition metal molybdenum, in molybdate form, is essential for plants as a number of enzymes use it to catalyze most important reactions in the nitrogen acclimatization, the synthesis of the phytohormone, degradation of the purine and the detoxification of the sulfite.
There are more than known 50 different enzymes that need Mo, whether direct or indirect impacts on plant growth and development, primarily phytohormones and the N-metabolism involving processes.



Molybdenum deficiency in plants

Molybdenum (Mo) is one of the six ‘minor’ chemical elements required by green plants.
The other five are iron, copper, zinc, manganese and boron.
These elements are termed ‘minor’ because plants need them in only very small amounts (in comparison with the ‘major’ elements nitrogen, phosphorus,potassium, sulfur, calcium and magnesium).
But they are essential for normal growth.
Of these six minor elements, molybdenum is needed in smaller quantities than any of the others.
As little as 50 grams of molybdenum per hectare will satisfy the needs of most crops.
Molybdenum is often present in farmyard manure, in seeds or other planting material such as tubers and corms, and as impurities in some artificial fertilisers.
The molybdenum supply from the seed appears to be significant only where the size of the seed is fairly large.
For example, the molybdenum content of bean, pea and maize seed can be important, but that of tomato seed is probably of little significance

SOIL ACIDITY
Molybdenum in acid soils tends to be unavailable to plants. This is why most molybdenum deficiencies occur on acid, rather than on neutral or alkaline soils.
A few cases of molybdenum deficiency have been reported on soils with a pH above 6.0, but most occur where pH is 5.5 or less.
(Note: On the pH scale 7.0 is neutral. Less than 7 indicates acidity, and above 7.0 alkalinity.)

FUNCTION IN PLANTS
Molybdenum is needed by plants for chemical changes associated with nitrogen nutrition.
In non-legumes (such as cauliflowers, tomatoes, lettuce, sunflowers and maize), molybdenum enables the plant to use the nitrates taken up from the soil.
Where the plant has insufficient molybdenum the nitrates accumulate in the leaves and the plant cannot use them to make proteins.
The result is that the plant becomes stunted, with symptoms similar to those of nitrogen deficiency.
At the same time, the edges of the leaves may become scorched by the accumulation of unused nitrates.
In legumes such as clovers, lucerne, beans and peas, molybdenum serves two functions.
The plant needs it to break down any nitrates taken up from the soil—in the same way as non-legumes use molybdenum.
And it helps in the fixation of atmospheric nitrogen by the root nodule bacteria.
Legumes need more molybdenum to fix nitrogen than to utilise nitrates.

SYMPTOMS
The main symptoms of molybdenum deficiency in non-legumes are stunting and failure of leaves to develop a healthy dark green colour.
The leaves of affected plants show a pale green or yellowish green colour between the veins and along the edges.
In advanced stages, the leaf tissue at the margins of the leaves dies.
The older leaves are the more severely affected.
In cauliflowers, the yellowing of the tissue on the outer leaves is followed by the death of the edges of the small heart leaves.
When these develop, the absence of leaf tissue on their edges results in the formation of narrow, distorted leaves to which the name ‘whiptail’ has been applied.
Affected leaves are usually slightly thickened and the leaf edges tend to curl upwards, especially in tomatoes.
It has been mentioned that legumes such as peas and beans need molybdenum either for utilisation of nitrates (as do non-legumes), or for nitrogen fixation by root nodule bacteria.
Where molybdenum is deficient, and adequate nitrogen is available from fertilisers applied to the soil, symptoms of molybdenum deficiency are similar to those seen in non-legumes, namely, interveinal and marginal leaf chlorosis followed by death of the tissue on the leaf margins.
These symptoms are seen in a condition found in french beans in the Gosford district, to which the name ‘scald’ has been applied.
In lucerne, clover and other pasture legumes, the main symptoms are associated with an inability to fix atmospheric nitrogen.
This stunting and yellowing is identical with nitrogen deficiency and resembles legumes having no nodules and grown in poor soils.

DIAGNOSIS
In some crops, especially cauliflowers, there are very characteristic molybdenum deficiency symptoms.
In others it is not always possible to diagnose with certainty whether a plant or a crop is suffering from a low supply of molybdenum.
The best way to find out is to apply a solution of sodium molybdate or ammonium molybdate to the leaves of the plants or to the soil at their base, and see whether there is any response.
This would be in the form of improved growth or development of a healthy leaf colour, compared with similar, untreated plants.
Certain chemical tests can help diagnose molybdenum deficiency.
In addition, the following can often help determine whether it is worthwhile making a trial application of molybdenum:
• Occurrence of whiptail in cauliflowers in the same locality.
Cauliflowers have a high molybdenum requirement.
If they are growing well on an unlimed soil, and without any trace of whiptail disease, it is unlikely that other crops in that area would suffer from molybdenum deficiency.
• Soil acidity. As mentioned earlier, molybdenum deficiency is more likely on acid soils having a pH of 5.5 or less
• Use of farmyard manure. Where large amounts of farmyard manure have been used, molybdenum deficiency is less likely.
• Patchy distribution of affected plants. Patchy distribution is characteristic of molybdenum deficiency.
The whole crop may be affected, but it is much more usual to find patches of affected plants in an otherwise healthy crop, or vice versa.

CONTROL
In most soils, molybdenum present in an unavailable form will be released by applying lime or dolomite.
The effect of liming on molybdenum availability is slow and it may take several months to correct the deficiency.
The amounts of lime or dolomite needed may range from 2 to 8 tonnes per hectare, depending on initial pH of the soil and whether it is sandy or heavy textured.
Unless lime is likely to be beneficial for other reasons, it is quicker and cheaper to apply a molybdenum compound to the soil or to the crop.
Where one of the molybdenum compounds is used, the quantities recommended vary from 75 g to 1 kg/ ha depending on the crop and the molybdenum material.
Molybdenum can be applied in the following ways:
• mixed with fertiliser; or
• in solution, to — seedlings in the seedbed before transplanting; — the leaves of plants in the field; or — the soil at the base of plants in the field.


CROP RECOMMENDATIONS
Clovers and lucerne Molybdenum trioxide (or equivalent amounts of sodium molybdate or ammonium molybdate): 75 g/ ha mixed with superphosphate. Vegetable crops
(a) Mixed with fertiliser. Ammonium molybdate or sodium molybdate, 1 kg/ha.
(b) Seedbed application to crops such as cauliflower, broccoli, cabbage and tomato.
Ammonium molybdate or sodium molybdate, 40 g dissolved in 50 L water and watered on to each 10 m2 of seedbed about one to two weeks before transplanting.
(Following such seedbed applications, cauliflower seedlings often develop a distinct blue colour in the stems and leaves.
This blue colour gradually disappears when they are transplanted.)
(c) Field application to growing crops. About 50 g of ammonium molybdate or sodium molybdate in 100 L water.
This may be sprayed onto the leaves of plants such as tomatoes and beans or it can be applied to the ground at the base of the plants, giving each cauliflower or tomato plant about 150 mL of solution.
These recommendations are usually more than enough to supply the molybdenum requirements of crops.
Lower rates may be adequate, but more than the recommended rate is a waste of money, and may injure the plants.

Mo COMPOUNDS AVAILABLE
Molybdenum compounds used for crops include molybdenum trioxide, sodium molybdate and ammonium molybdate.
Choice of the material to be used depends on whether it is to be applied with fertilizer or as a solution Molybdenum trioxide is only partially soluble in water.
It is the form usually used in molybdenized superphosphate but is not suitable for making up sprays to treat a growing crop.
Molybdenum trioxide (also called molybdic oxide) contains 66 per cent molybdenum.
Ammonium molybdate contains 54 per cent molybdenum.
Though it is soluble in water, it is frequently sold in large lumps which dissolve slowly in cold water.
It is better either to use hot water to dissolve the lumps or to crush them to a fine powder before adding to the water
Sodium molybdate is usually sold in a form containing 39 per cent molybdenum.
It is sold as fine crystals which dissolve readily in cold water and this material is undoubtedly the most convenient for the preparation of solutions to be used for spraying


Sodium Molybdate is a free flowing soluble crystalline fertiliser and is used to supply the trace element molybdenum to crops and livestock in various situations.
Sodium Molybdate is only required in very small quantities to satisfy annual plant requirements.
Sodium Molybdate is suitable for foliar or fertigation application on a wide range of horticultural and broad acre crops and pastures.


SODIUM MOLYBDATE BENEFITS
• Supplies the essential trace element molybdenum to crops and livestock
• Foliar applied to crops and pastures grown on acid soils where plant availability is low
• Essential for conversion of nitrates in leaves to amino acids and proteins
• Suitable for foliar or fertigation
• Ideal for brassica, beans, peas, grapes, cucurbits, canola, clover and other crops and pastures susceptible to molybdenum deficiency.

SODIUM MOLYBDATE
Sodium Molybdate Sodium molybdate, Na2MoO4, is useful as a source of molybdenum.[2] It is often found as the dihydrate, Na2MoO4·2H2O. The molybdate(VI) anion is tetrahedral. Two sodium cations coordinate with every one anion. Sodium Molybdate is a crystalline powder essential for the metabolism and development of plants and animals as a cofactor for enzymes. History Sodium molybdate was first synthesized by the method of hydration.[4] A more convenient synthesis is done by dissolving MoO3 in sodium hydroxide at 50–70 °C and crystallizing the filtered product.[3] The anhydrous salt is prepared by heating to 100 °C. MoO3 + 2NaOH + H2O → Na2MoO4·2H2O Uses The agriculture industry uses 1 million pounds per year as a fertilizer. In particular, its use has been suggested for treatment of whiptail in broccoli and cauliflower in molybdenum-deficient soils.[5][6] However, care must be taken because at a level of 0.3 ppm sodium molybdate can cause copper deficiencies in animals, particularly cattle.[3] It is used in industry for corrosion inhibition, as it is a non-oxidizing anodic inhibitor.[3] The addition of sodium molybdate significantly reduces the nitrite requirement of fluids inhibited with nitrite-amine, and improves the corrosion protection of carboxylate salt fluids.[7] In industrial water treatment applications where galvanic corrosion is a potential due to bimetallic construction, the application of sodium molybdate is preferred over sodium nitrite. Sodium molybdate has the advantage in that the dosing of lower ppm's of molybdate allow for lower conductivity of the circulating water. Sodium molybdate at levels of 50-100 ppm offer the same levels of corrosion inhibition that sodium nitrite at levels of 800+ ppm. By utilizing lower concentrations of sodium molybdate, conductivity is kept at a minimum and thus galvanic corrosion potentials are decreased. Reactions When reacted with sodium borohydride, molybdenum is reduced to lower valent molybdenum(IV) oxide: Na2MoO4 + NaBH4 + 2H2O → NaBO2 + MoO2 + 2NaOH + 3H2 Sodium molybdate reacts with the acids of dithiophosphates: Na2MoO4 + (R = Me, Et)(RO)2PS2H → [MoO2(S2P(OR)2)2] which further reacts to form [MoO3(S2P(OR)2)4]. Compound Formula H4Na2MoO6 Molecular Weight 241.95 Appearance White powder or crystals Melting Point 100 °C Boiling Point N/A Density 2.37 g/cm3 Solubility in H2O N/A Exact Mass 243.885735 Monoisotopic Mass 243.885735 Chemical Identifiers Linear Formula Na2MoO4 • 2H2O MDL Number MFCD00149170 EC No. 231-551-7 Pubchem CID 16211258 IUPAC Name disodium; dioxido(dioxo)molybdenum; dihydrate SMILES [Na+].[Na+]. O.O.[O-][Mo] ([O-])(=O)=O InchI Identifier InChI=1S/Mo.2Na.2H2O.4O/h;;;2*1H2;;;;/q;2*+1;;;;;2*-1 InchI Key FDEIWTXVNPKYDL-UHFFFAOYSA-N Safety Sodium molybdate is incompatible with alkali metals, most common metals and oxidizing agents. It will explode on contact with molten magnesium. It will violently react with interhalogens (e.g., bromine pentafluoride; chlorine trifluoride). Its reaction with hot sodium, potassium or lithium is incandescent. It is a molybdenum transition metal and in its pure form it is silvery white in color and very hard. Its melting temperature is quite high. Further hardening of the steel can be achieved by adding a small amount. Molybdenum is also important in the nutrition of plants and is involved in some enzymes. Swedish chemist Carl Wilhelm Scheele showed in 1778 that the mineral (molybdenite), which was previously thought to be a lead ore or graphite, was a sulfur compound of an unknown metal. Swedish chemist Peter Jacob Hjelm also separated molybdenum into metal in 1782 and named it after the Greek word molybdos, which means "like lead". Although molybdenum is found in minerals such as wulfenite (PbMoO4) or powellite (CaMoO4), the main commercial source of molybdenum is molybdenite (MoS2). Molybdenum can also be obtained by direct mining and as a byproduct during copper mining. Molybdenum is found in its ores in amounts varying from 0.01% to 0.5%. About half of the world's molybdenum mining is carried out in the USA (Phelps Dodge Corporation). Molybdenum, which is similar to chromium and wolfram in terms of chemical properties; It has superior properties such as high melting and boiling point, high heat resistance, high thermal conductivity and low thermal expansion. Molybdenum melts at 2623 ° C. With this feature, it takes the sixth place among metals. Molybdenum boiling at 4639 ° C is not affected by air in cold, oxidized in incandescent state, affected by nitric and sulfuric acids, decomposes water vapor at high temperatures. The density of molybdenum is 10.28 gr / cm3. Usage areas The agricultural industry uses up to £ 1 million a year of fertilizer. In particular, it has been suggested to be used for processing broccoli and cauliflower seeds in molybdenum deficient soils. However, caution should be exercised as sodium molybdate at a level of 0.3 ppm can cause copper deficiencies in animals, especially cattle. It is used in industry for corrosion prevention because it is a non-oxidizing anodic inhibitor. The addition of sodium molybdate significantly reduces the nitrite requirement of nitrite-amine inhibited liquids and improves the corrosion protection of carboxylate salt fluids. In industrial water treatment applications where galvanic corrosion is potential due to the bimetal structure, sodium molybdate application is preferred over sodium nitrite. Sodium molybdate has the advantage that lower ppm molybdate dosing has lower conductivity of circulating water. Sodium molybdate at 50-100 ppm levels offers the same levels of corrosion inhibition as sodium nitrite at 800+ ppm levels. By using lower concentrations of sodium molybdate, conductivity is kept to a minimum, thus reducing galvanic corrosion potential Sodium Molybdate Dihydrate is generally immediately available in most volumes. Hydrate or anhydrous forms may be purchased. High purity, submicron and nanopowder forms may be considered. American Elements produces to many standard grades when applicable, including Mil Spec (military grade); ACS, Reagent and Technical Grade; Food, Agricultural and Pharmaceutical Grade; Optical Grade, USP and EP/BP (European Pharmacopoeia/British Pharmacopoeia) and follows applicable ASTM testing standards. Typical and custom packaging is available. Additional technical, research and safety (MSDS) information is available as is a Reference Calculator for converting relevant units of measurement. WHAT IS SODIUM MOLYBDATE? There are two main forms of Sodium Molybdate. Sodium Molybdate, Dihydrate is a crystalline powder. It loses its water of crystallization at 100 degrees Celsius. It is known to be less toxic than the other corresponding compounds of group 6B elements in the periodic table. Sodium Molybdate, Dihydrate is used in the manufacturing of inorganic and organic pigments, as a corrosion inhibitor, as a bath additive for finishing metals finishing, as a reagent for alkaloids, and as an essential micronutrient for plants and animals. Sodium Molybdate, Anhydrous is a small, lustrous, crystalline plate. It has the melting point of 687 degrees Celsius and a density of 3.28 (18C). It is soluble in water and also noncombustible. It can be used for reagent in analytical chemistry, paint pigment, production of molybdated toners and lakes, metal finishing, brightening agent for zinc plating, corrosion inhibitor, catalyst in dye and pigment production, additive for fertilizers and feeds, and micronutrient. WHY THE AGRICULTURE INDUSTRY USES SODIUM MOLYBDATE Sodium Molybdate uses cover a wide range of fields, including manufacturing, metalwork, printing, and more. But the impact it can have on plants and animals has brought it into the forefront of use for the agriculture industry, to the tune of more than 1 million pounds of sodium molybdate fertilizer used per year. The basic chemistry of a molybdate, such as sodium molybdate, contains the element molybdenum in its highest oxidation state, which in turn helps contribute to a high solubility of the chemical in water, a benefit in fertilizer application. This characteristic, when combined with sodium molybdate’s use as a delivery vessel for essential micronutrients (such as molybdenum) in plants, serves as another key reason for the choice of sodium molybdate fertilizer over other types of fertilizers used in agriculture. Another touchpoint for this usage ties back to the hydroponic nutrient practice that is growing in popularity. Hydroponics is an agricultural method in which plants are grown without soil. Instead, they receive their essential micronutrients through a water solvent, a practice that has shown growth rates almost 50 percent faster than traditional soil-grown plants, in addition to a higher yield from hydroponic plants. Sodium molybdate has seen a particularly strong uptick in usage among farmers of leguminous plants, such as alfalfa, peas, beans, lentils and peanuts. Included in fertilizer, it provides these plants with enhanced uptake of the essential nitrogen element, while also allowing for efficient fixing of atmospheric nitrogen found in the atmosphere by bacteria in the legumes. These bacteria convert the nitrogen into ammonia to synthesize amino acids within the plant. Overall, the use of sodium molybdate in the agricultural industry can be summarized in that it is one of the few chemicals that can provide essential micronutrients and help drive plant function in a form that is both efficient and effective. Efficiency is shown not only by the relatively small amounts needed to make an impact on the treated plants, but also in the ability to administer the chemical in easily-absorbed water-based formats. Use of Sodium Molybdate Dihydrate as an Efficient Heterogeneous Catalyst for the Synthesis of Benzopyranopyrimidine Derivatives Sodium molybdate dihydrate (Na2MoO4.2H2O) has been investigated as a heterogeneous catalyst for the one-pot pseudo–four-component synthesis of the benzopyranopyrimidine derivatives. This efficient and facile technique avoids the use of difficult workup and harsh reaction conditions. SODIUM MOLYBDATE Sodium Molybdate is a free flowing soluble crystalline fertiliser and is used to supply the trace element molybdenum to crops and livestock in various situations. Sodium Molybdate is only required in very small quantities to satisfy annual plant requirements. Sodium Molybdate is suitable for foliar or fertigation application on a wide range of horticultural and broad acre crops and pastures. SODIUM MOLYBDATE BENEFITS • Supplies the essential trace element molybdenum to crops and livestock • Foliar applied to crops and pastures grown on acid soils where plant availability is low • Essential for conversion of nitrates in leaves to amino acids and proteins • Suitable for foliar or fertigation • Ideal for brassica, beans, peas, grapes, cucurbits, canola, clover and other crops and pastures susceptible to molybdenum deficiency. Application Sodium Molybdate can be used as a foliar or fertigation application in a regular nutrition program for applicable crops and pastures. Multiple applications may be required if leaf analyses reveal ongoing deficiency. Note: Molybdenum can be toxic when levels become too high. One spray per crop is generally sufficient, except where deficiency is noted. Susceptible crops such as brassicas and cucurbits may require two sprays three weeks apart Molybdate Stabilization It is well known that sodium molybdate forms stable complexes with thiols (Kay and Mitchell, 1968; Kaul et al., 1987). Ever since Pratt described the ability of molybdate to stabilize the steroid binding activity of receptors, and to block activation (or transformation) (Leach et al., 1979), it has been suspected that molybdate exerted its effects by interacting with cysteines of the receptor. A series of indirect experiments led to the postulate that the sequence of 644–671, and especially cysteines 656 and 661, were required for molybdate stabilization (Dalman et al., 1991a). Experiments with receptor fragments of wild-type and mutant receptors have supported the involvement of this region. However, they have also ruled out the involvement of Cys-656 and 661 in any of molybdate’s effects (Modarress et al., 1994) (see Section III,E,4). Chemicals Cobalt thiocyanate, cobalt acetate dihydrate, glacial acetic acid, isopropylamine, acetaldehyde, ammonium vanadate, formaldehyde, para-dimethylaminobenzaldehyde, ferric chloride, vanillin, sodium molybdate, selenius acid, copper sulfate pentahydrate, sodium nitroprusside, 2-chloroacetophenone, and sodium carbonate were purchased from Sigma-Aldrich Chemical (St. Louis, MO, USA). Methanol, hexane, and chloroform were obtained from Burdick and Jackson (Muskegon, MI, USA). Hydrochloric acid, sulfuric acid, nitric acid, and pyridine were purchased from Mallinckrodt Baker, (Paris, KY, USA). Ethanol was obtained from Quantum Chemical (Tuscola, IL, USA). The drugs were purchased in powder form from Sigma-Aldrich Chemical (St. Louis, MO, USA), Alltech-Applied Science (State College, PA, USA) or Research Triangle Institute (RTI, NC, USA). Animal Water-insoluble molybdenite (MoS2) is practically nontoxic; rats dosed with up to 500 mg molybdenite daily for 44 days exhibited no adverse effects. In contrast, animals dosed subchronically with water-soluble molybdenum compounds exhibited gastrointestinal disturbances, growth retardation, anemia, hypothyroidism, bone and joint deformities, liver and kidney abnormalities, and death. Fifty percent mortality was reported in rats maintained for 40 days on molybdenum-enhanced diets containing 125 mg Mo kg−1 (as molybdenum trioxide, MoO3), 100 mg Mo kg−1 (as calcium molybdate, CaMoO4), or 333 mg Mo kg−1 (as ammonium molybdate, (NH4)2MoO4). A dietary level of 0.1% sodium molybdate (Na2MoO4·2H2O) for several weeks was lethal to rabbits. Growth retardation was observed in rats maintained on diets containing 0.04–0.12% molybdenum. Evidence that the toxic effects of molybdenum might be caused by a secondarily acquired copper deficiency was shown in a study where a significant reduction in growth occurred in rats after 11 weeks on a diet containing 20 ppm molybdenum and 5 ppm copper; whereas, growth was not affected by molybdenum dietary levels as high as 80 ppm when the dietary level of copper was increased to 20 ppm. Hypothyroidism, as evidenced by decreased levels of plasma thyroxin, was found in rabbits maintained on a diet containing 0.3% Mo (as sodium molybdate) for several weeks or longer. Anemia, as well as anorexia, weight loss, alopecia, and bone deformities occurred in young rabbits maintained for 4–17 weeks on a diet containing 0.1% molybdenum (as sodium molybdate). Anemia was also observed in rats maintained on a diet containing 0.04% Mo (as sodium molybdate) for 5 weeks, in rabbits on a dietary level of 0.2% sodium molybdate for 5 weeks, and in chicks on a dietary level of 0.4% sodium molybdate for 4 weeks. Signs of anemia and marked erythroid hyperplasia of the bone marrow were observed in rabbits maintained for 11 days on a diet containing 0.4% sodium molybdate. Bone and connective tissue disorders observed in animals receiving dietary levels of molybdenum 0.04% for 4 weeks or longer included mandibular exostoses, joint deformities, detachment of tendons, epiphyseal line fractures, and epiphyseal plate widening. Acute and Short-Term Toxicity There is considerable variability in the toxicity of molybdenum, depending on the chemical form and the animal species. Generally, soluble compounds are more toxic than insoluble compounds. In animals, acutely toxic oral doses of molybdenum result in severe gastrointestinal irritation with diarrhea, coma, and death from cardiac failure. The rat oral lethal doses (LD50s) values are 188 mg kg−1 for molybdenum trioxide, and 680 mg kg−1 for ammonium molybdate. The LD50 for water-insoluble molybdentite (MoS2) is >500 mg kg−1 and exposures at this level for 44 days exhibited no adverse effects. Oral subchronic median LD50s for molybdenum oxide, calcium molybdate, and ammonium molybdate in rats were 125, 101, and 330 mg kg−1 day−1, respectively, with deaths occurring over a period of 8–232 days. Molybdenum compounds produce varying degrees of eye and skin irritation, with molybdenum trioxide producing eye and respiratory irritation. Rabbits exposed to dietary doses of ammonium molybdate at 0.025, 0.5, 5, and 50 mg kg−1 day−1 for 6 months resulted in liver changes that generated a NOAEL of 0.5 mg kg−1 day−1. Guinea pigs are a less-sensitive species after dietary exposure to sodium molybdate for 8 weeks yielded a LOAEL of 75 mg kg−1 day−1. Anemia, as well as anorexia, weight loss, alopecia, and bone deformities occurred in young rabbits maintained for 4–17 weeks on a diet containing 0.1% molybdenum (as sodium molybdate). Anemia was also observed in rats maintained on a diet containing 0.04% Mo (as sodium molybdate) for 5 weeks, in rabbits on a dietary level of 0.2% sodium molybdate for 5 weeks, and in chicks on a dietary level of 0.4% sodium molybdate for 4 weeks. Signs of anemia and marked erythroid hyperplasia of the bone marrow were observed in rabbits maintained for 11 days on a diet containing 0.4% sodium molybdate. Bone and connective tissue disorders observed in animals receiving dietary levels of molybdenum 0.04% for 4 weeks or longer included mandibular exostoses, joint deformities, detachment of tendons, epiphyseal line fractures, and epiphyseal plate widening. Medium formulation Chemostat glucose-limited synthetic minimal media contains (per liter) 0.1 g calcium chloride, 0.1 g sodium chloride, 0.5 g magnesium sulfate, 1 g potassium phosphate monobasic, 5 g ammonium sulfate, 500 μg boric acid, 40 μg copper sulfate, 100 μg potassium iodide, 200 μg ferric chloride, 400 μg manganese sulfate, 200 μg sodium molybdate, 400 μg zinc sulfate, 1 μg biotin, 200 μg calcium pantothenate, 1 μg folic acid, 1 mg inositol, 200 μg niacin, 100 μg p-aminobenzoic acid, 200 μg pyridoxine, 100 μg riboflavin, 200 μg thiamine, and 0.08% glucose. Medium is prepared in 10 l quantities, mixed thoroughly, and filter sterilized into an autoclaved glass carboy. Carboy has an outlet port at bottom, leading to a small piece of tubing with a luer lock connector at the end. All entry and exit ports are covered with foil before autoclaving. Outflow tubing is sealed with a metal clamp before filling. Carboy is placed on a shelf above chemostat area. Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on safety and efficacy of sodium molybdate dihydrate for sheep, based on a dossier submitted for the re‐evaluation of the additive. The additive is currently authorised in the EU for all animal species as ‘Nutritional additive’ – ‘Compounds of trace elements’. Taking the optimal Cu:Mo ratio of 3–10, and the highest total copper level authorised in complete feeds for sheep (15 mg/kg), the FEEDAP Panel concluded that 2.5 mg total Mo/kg complete feed is safe for sheep. Considering (i) a safe intake of 0.6 mg Mo/day, (ii) the estimate average intake figure from food in Europe (generally less than 100 μg/day), (iii) the contribution of foods of animal origin to the total molybdenum intake (estimated to be up to 22 %), and (iv) that molybdenum would not accumulate in edible tissues/products of sheep fed molybdenum supplemented diets up to the upper safe level, the FEEDAP Panel concluded that the use of sodium molybdate as a additive in sheep at 2.5 mg total Mo/kg complete feed is safe for consumers. The additive under assessment feed poses no risk by inhalation to users; it is a skin and eye irritant, but it is not considered as a skin sensitiser. Sodium molybdate used up to 2.5 mg Mo/kg complete sheep feed poses no concerns for the safety for the environment. The FEEDAP Panel recognises that molybdenum does not need to be added to diets to cover the nutritional needs of molybdenum of sheep. Molybdenum supplementation in sheep feed is considered effective in order to guarantee an adequate balance with copper, when the Cu:Mo ratio in the diet is in the range 3–10. Summary Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on safety and efficacy of sodium molybdate dihydrate for sheep. The additive is currently authorised in the European Union (EU) under the element Molybdenum‐Mo (E7) for all animal species; the compound is included in the EU Register of Feed Additives under the category ‘Nutritional additives’ and the functional group ‘Compounds of trace elements’. Molybdenum toxicity in farm animals is manifested as antagonism of absorption and/or biological activity of copper, and is greatly enhanced by high sulfur content in the diet. Ruminants, including sheep, are highly susceptible to molybdenum excess, which may induce a clinically severe copper deficiency (molybdenosis). Conversely, low molybdenum in the diet is expected to enhance copper toxicity, if the intake of copper is high. The FEEDAP Panel considered therefore not possible to establish an absolute figure for a dietary molybdenum concentration which is equally safe for sheep and effective in preventing copper toxicity. Considering that (i) the key parameter to ensure the safety of molybdenum supplementation is the optimal Cu:Mo ratio, which in sheep is in the range of 3–10 and (ii) the highest total copper level authorised in complete feeds for sheep is 15 mg/kg, the FEEDAP Panel concluded, that 2.5 mg total Mo/kg complete feed is safe for sheep. Toxicokinetic data in laboratory rodents and farm animals (including sheep), however incomplete, uniformly indicate that molybdenum would not accumulate in edible tissues or products of sheep fed molybdenum supplemented diets up to the upper maximum level of 2.5 mg/kg. The FEEDAP Panel considered that the available data support an upper intake tolerable level (UL) of 0.01 mg/kg body weight (bw) for molybdenum based on the no observed adverse effect level (NOAEL) for female reproductive toxicity and developmental toxicity of 0.9 mg/kg bw per day and the application of a 100‐safety factor. The UL would result in a safe intake of 0.6 mg/day in a 60‐kg individual; this intake is largely higher than the estimate average intake figure from food in Europe (generally less than 100 μg/day). Molybdenum is ubiquitous in foods, surveys in the EU countries provide average intake figures generally lower than 100 μg/day, whereas offals (liver and kidney) are relatively rich sources of molybdenum, the contribution of foods of animal origin to the total molybdenum intake has been estimated to be up to 22%. Molybdenum would not accumulate in edible tissues or products of sheep fed molybdenum supplemented diets up to the upper maximum level of 2.5 mg/kg. Therefore, the FEEDAP Panel considered that the use of sodium molybdate as a feed additive in sheep at 2.5 mg Mo/kg complete feed is safe for consumers. Molybdenum is a potential respiratory toxicant; the available data indicate that the use of the sodium molybdate under evaluation in animal nutrition poses no risk by inhalation to users. The additive is a skin and eye irritant, but it is not considered as a skin sensitiser. The use of sodium molybdate as a feed additive in sheep up to maximum of 2.5 mg of Mo/kg complete feed poses no concerns for the safety for the environment. The FEEDAP Panel recognises that molybdenum does not need to be added to diets to cover the nutritional needs of molybdenum of sheep. Molybdenum supplementation in sheep feed is considered effective in order to guarantee an adequate balance with copper, when the Cu:Mo ratio in the diet is in the range 3–10. Additional information The additive ‘Sodium molybdate’ had been authorised in the European Union (EU) under the element Molybdenum‐Mo (E7) for all animal species ‘Without a time limit’ (Council Directive 70/524/EEC concerning additives in feedingstuffs – List of authorised additives in feedingstuffs (2004/C 50/01). Following the provisions of Article 10(1) of Regulation (EC) No 1831/2003 the compound was included in the EU Register of Feed Additives under the category ‘Nutritional additives’ and the functional group ‘Compounds of trace elements’. The Scientific Committee on Food (SCF) of the European Commission published in the year 2000 an opinion on the tolerable upper intake levels of molybdenum (European Commission, 2000). The EFSA Panel on Food Additives and Nutrient Sources added to Food (ANS Panel) delivered an opinion on potassium molybdate as a source of molybdenum added for nutritional purposes to food supplements (EFSA, 2009). The EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA Panel) delivered an opinion on dietary reference values for molybdenum (EFSA NDA Panel, 2013). According to Regulation (EC) no 1170/20092, Molybdenum is listed as mineral which may be used in the manufacture of food supplements (Annex I); the following molybdenum compounds are authorised for use in the manufacture of food supplements: ammonium molybdate (molybdenum (VI)), potassium molybdate (molybdenum (VI)) and sodium molybdate (molybdenum (VI)) (Annex II); the following molybdenum compounds are authorised as mineral substances which may be added to foods: ammonium molybdate (molybdenum (VI)) and sodium molybdate (molybdenum (VI)) (Annex III). The following molybdenum compounds may be added for specific nutritional purposes in foods for particular nutritional uses (Commission Regulation (EC) No 953/2009)3: ammonium molybdate and sodium molybdate. The following types of fertilisers containing molybdenum and described as ‘Fertilisers containing only one micro‐nutrient’ are listed in Annex I of Regulation (EC) No 2003/2003 of the European Parliament and of the Council4 as: (a) sodium molybdate (chemically obtained product containing sodium molybdate as its essential ingredient), (b) ammonium molybdate (chemically obtained product containing ammonium molybdate as its essential ingredient), (c) molybdenum‐based fertiliser Product obtained by mixing types (a) and (b)), and (d) molybdenum‐based fertiliser solution (product obtained by dissolving types ‘(a)’ and/or one of the type ‘(b)’ in water). Effects on skin and eye No original studies were provided by the applicant. The potential of sodium molybdate to elicit skin and ocular irritation or skin sensitization were briefly reviewed in (European Commission, 2000). When tested in rabbits, sodium molybdate (anhydrous form) elicited evident skin irritation for 24 h after application, albeit the skin lesions reversed within 72 . In an eye irritation test on rabbits, a 20% solution did not increase corneal irritation but caused evident conjunctival redness. Based on these findings, sodium molybdate is considered as a skin and eye irritant. The substance is reported not to elicit skin sensitisation (European Commission, 2000 and references herein). Sodium molybdate, Na2MoO4, is useful as a source of molybdenum. It is often found as the dihydrate, Na2MoO4·2H2O. The molybdate(VI) anion is tetrahedral. Two sodium cations coordinate with every one anion. Sodium Molybdate is a crystalline powder essential for the metabolism and development of plants and animals as a cofactor for enzymes. Sodium molybdate (anhydrous) is an inorganic sodium salt having molybdate as the counterion. It has a role as a poison. It contains a molybdate. General description Sodium molybdate dihydrate (SMD) is a molybdic acid disodium salt. It crystallizes in the orthorhombic space group, Pbca.[1] The toxic effect of SMD on the avian species, northern bobwhite quail has been investigated.[2] Its ability to inhibit corrosion of 6082 wrought aluminum alloy has been studied in NaCl solution of chlorosulfonic acid.[3] Application Sodium molybdate dihydrate has been used as one of the phosphatase inhibitor during the Western blot analysis.[4] It may be used to prepare: • Shuttle-like barium molybdate (BaMoO4) microstructures under microwave conditions.[5] • Nickel-molybdenum-zinc (NiMoZn) electrode.[6] • Eu3+ doped lead molybdate (PbMoO4) nanocrystals (NCs) under microwave conditions. Sodium molybdate was first synthesized by the method of hydration.[4] A more convenient synthesis is done by dissolving MoO3 in sodium hydroxide at 50–70 °C and crystallizing the filtered product.[3] The anhydrous salt is prepared by heating to 100 °C. Uses The agriculture industry uses 1 million pounds per year as a fertilizer. In particular, its use has been suggested for treatment of whiptail in broccoli and cauliflower in molybdenum-deficient soils.[5][6] However, care must be taken because at a level of 0.3 ppm sodium molybdate can cause copper deficiencies in animals, particularly cattle.[3] It is used in industry for corrosion inhibition, as it is a non-oxidizing anodic inhibitor.[3] The addition of sodium molybdate significantly reduces the nitrite requirement of fluids inhibited with nitrite-amine, and improves the corrosion protection of carboxylate salt fluids.[7] In industrial water treatment applications where galvanic corrosion is a potential due to bimetallic construction, the application of sodium molybdate is preferred over sodium nitrite. Sodium molybdate has the advantage in that the dosing of lower ppm's of molybdate allow for lower conductivity of the circulating water. Sodium molybdate at levels of 50-100 ppm offer the same levels of corrosion inhibition that sodium nitrite at levels of 800+ ppm. By utilizing lower concentrations of sodium molybdate, conductivity is kept at a minimum and thus galvanic corrosion potentials are decreased. Sodium molybdate is incompatible with alkali metals, most common metals and oxidizing agents. It will explode on contact with molten magnesium. It will violently react with interhalogens (e.g., bromine pentafluoride; chlorine trifluoride). Its reaction with hot sodium, potassium or lithium is incandescent. Usage areas The agricultural industry uses up to £ 1 million a year of fertilizer. In particular, it has been suggested to be used for processing broccoli and cauliflower seeds in molybdenum deficient soils. However, caution should be exercised as sodium molybdate at a level of 0.3 ppm can cause copper deficiencies in animals, especially cattle. It is used in industry for corrosion prevention because it is a non-oxidizing anodic inhibitor. The addition of sodium molybdate significantly reduces the nitrite requirement of nitrite-amine inhibited liquids and improves the corrosion protection of carboxylate salt fluids. In industrial water treatment applications where galvanic corrosion is potential due to the bimetal structure, sodium molybdate application is preferred over sodium nitrite. Sodium molybdate has the advantage that lower ppm molybdate dosing has lower conductivity of circulating water. Sodium molybdate at 50-100 ppm levels offers the same levels of corrosion inhibition as sodium nitrite at 800+ ppm levels. By using lower concentrations of sodium molybdate, conductivity is kept to a minimum, thus reducing galvanic corrosion potential Sodium Molybdate Dihydrate is generally immediately available in most volumes. Hydrate or anhydrous forms may be purchased. High purity, submicron and nanopowder forms may be considered. American Elements produces to many standard grades when applicable, including Mil Spec (military grade); ACS, Reagent and Technical Grade; Food, Agricultural and Pharmaceutical Grade; Optical Grade, USP and EP/BP (European Pharmacopoeia/British Pharmacopoeia) and follows applicable ASTM testing standards. Typical and custom packaging is available. Additional technical, research and safety (MSDS) information is available as is a Reference Calculator for converting relevant units of measurement. WHAT IS SODIUM MOLYBDATE? There are two main forms of Sodium Molybdate. Sodium Molybdate, Dihydrate is a crystalline powder. It loses its water of crystallization at 100 degrees Celsius. It is known to be less toxic than the other corresponding compounds of group 6B elements in the periodic table. Sodium Molybdate, Dihydrate is used in the manufacturing of inorganic and organic pigments, as a corrosion inhibitor, as a bath additive for finishing metals finishing, as a reagent for alkaloids, and
SODIUM MYRETH SULFATE
SYNONYMS Ethanol, 2-[2-[2-(tetradecyloxy)ethoxy]ethoxy]-, 1-(hydrogen sulfate), sodium salt (1:1);Ethanol, 2-[2-[2-(tetradecyloxy)ethoxy]ethoxy]-, hydrogen sulfate sodium salt;Ethanol, 2-[2-[2-(tetradecyloxy)ethoxy]ethoxy]-, hydrogen sulfate, sodium salt;Natrium-2-[2-[2-(tetradecyloxy)ethoxy]ethoxy]ethylsulfat;sodium 2-[2-[2-(tetradecyloxy)ethoxy]ethoxy]ethyl sulphate CAS NO:25446-80-4
SODIUM MYRISTATE
SODIUM MYRISTOYL GLUTAMATE N° CAS : 38517-37-2 / 38754-83-5 / 71368-20-2 Nom INCI : SODIUM MYRISTOYL GLUTAMATE Nom chimique : Sodium hydrogen N-(1-oxotetradecyl)-L-glutamate N° EINECS/ELINCS : 253-981-4 Compatible Bio (Référentiel COSMOS) Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation