Stearic Acid

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Stearic Acid STEARIC ACID www.pawarchemicals.com PRODUCT IDENTIFICATION CAS NO. 57-11-4 EINECS NO. 200-313-4 FORMULA CH3(CH2)16COOH MOL WT. 284.48 H.S. CODE 2915.70.0120 SMILES C(CCCCCCCCCCC)CCCCCC(=O)O TOXICITY SYNONYMS n-Octadecanoate; 1-Heptadecanecarboxylic acid; n-Octadecylic acid; Cetylacetic acid; Acide octadecylique; Acide stearique; Stearophanic acid; Octadecanoic acid; Other CAS RN: 8013-28-3, 8023-06-1, 8037-83-0, 8037-40-9, 8039-54-1, 8039-53-0, 8039-52-9, 8039-51-8, 39390-61-9, 58392-66-8, 82497-27-6, 134503-33-6, 197923-10-7, 294203-07-9 EXTRA NOTES EPA Pesticide Chemical Code 079082, FEMA No. 3035 CLASSIFICATION Fatty Acid PHYSICAL AND CHEMICAL PROPERTIES PHYSICAL STATE White to yellowish solid MELTING POINT 67 - 69 C BOILING POINT 361 SPECIFIC GRAVITY 0.94 SOLUBILITY IN WATER 0.1-1 g/100 ml at 23 C OH RATE 2.25E-11 (cm3/molecule-sec at 25 C Atmospheric ) VAPOR DENSITY 9.8 HENRY LAW CONSTANT 4.76E-07 (atm-m3/mole at 25 C) Constant Health: 1 Flammability: 1 Reactivity: 0 NFPA RATINGS REFRACTIVE INDEX FLASH POINT 196 C STABILITY Stable under ordinary conditions EXTERNAL LINKS &GENERAL DESCRIPTION Wikipedia Linking Material Safety Data Sheet Google Scholar Search GENERAL DESCRIPTION: Fatty Acids are aliphatic carboxylic acid with varying hydrocarbon lengths at one end of the chain joined to terminal carboxyl (-COOH) group at the other end. The general formula is R-(CH2)n-COOH. Fatty acids are predominantly unbranched and those with even numbers of carbon atoms between 12 and 22 carbons long react with glycerol to form lipids (fat-soluble components of living cells) in plants, animals, and microorganisms. Fatty acids all have common names respectively lauric (C12), myrIstic (C14), palmitic (C16), stearic (C18), oleic (C18, unsaturated), and linoleic (C18, polyunsaturated) acids. The saturated fatty acids have no double bonds, while oleic acid is an unsaturated fatty acid has one double bond (also described as olefinic) and polyunsaturated fatty acids like linolenic acid contain two or more double bonds. Lauric acid (also called Dodecanoic acid) is the main acid in coconut oil (45 - 50 percent) and palm kernel oil (45 - 55 percent). Nutmeg butter is rich in myristic acid (also called Tetradecanoic acid ) which constitutes 60-75 percent of the fatty-acid content. Palmitic acid(also called Hexadecylic acid ) constitutes between 20 and 30 percent of most animal fats and is also an important constituent of most vegetable fats (35 - 45 percent of palm oil). Stearic acid (also called Octadecanoic Acid) is nature's most common long-chain fatty acids, derived from animal and vegetable fats. It is widely used as a lubricant and as an additive in industrial preparations. It is used in the manufacture of metallic stearates, pharmaceuticals, soaps, cosmetics, and food packaging. It is also used as a softener, accelerator activator and dispersing agent in rubbers. Oleic acid (systematic chemical name is cis-octadec-9-enoic acid) is the most abundant of the unsaturated fatty acids in nature. Stearic Acid is widely used as a lubricant and as an additive in industrial preparations. It is used in the manufacture of metallic stearates, pharmaceuticals, soaps, cosmetics, and food packaging. It is also used as a softener, accelerator activator and dispersing agent in rubbers. INDIVIDUAL SATURATED FATTY ACIDS COMMON NAME SYSTEMATIC NAME CAS RN Length MELTING POINT n-Hendecanoic Acid 112-37-8 Straight 11:0 Undecylic Acid 30 C Lauric Acid n-Dodecanoic Acid 143-07-7 Straight 12:0 44 C 638-53-9 Straight 13:0 Tridecylic Acid n-Tridecanoic Acid 42 C Myristic Acid n-Tetradecanoic Acid 544-63-8 Straight 14:0 54 C Pentadecanoic Acid n-Pentadecanoic Acid 1002-84-2 Straight 15:0 52 C Palmitic Acid n-Hexadecanoic Acid 57-10-3 Straight 16:0 62 C 506-12-7 Straight 17:0 Margaric Acid n-Heptadecanoic Acid 61 C Stearic Acid n-Octadecanoic Acid 57-11-4 Straight 18:0 70 C 646-30-0 Straight 19:0 Nondecylic Acid n-Nonadecanoic Acid 70 C Arachidic Acid n-Eicosanoic Acid 506-30-9 Straight 20:0 75 C Henicosanoic acid 2363-71-5 Straight 21:0 n-Heneicosanoic Acid 74 C Behenic Acid 112-85-6 Straight 22:0 n-Docosanoic Acid 81 C Tricosanoic acid n-Tricosanoic acid 2433-96-7 Straight 23:0 80 C Lignoceric Acid n-Tetracosanoic Acid 557-59-5 Straight 24:0 85 C 506-38-7 Straight 25:0 Pentacosanoic Acid n-Pentacosanoic Acid 85 C Cerotinic acid n-Hexacosanoic acid 506-46-7 Straight 26:0 87 C 7138-40-1 Straight 27:0 Heptacosanoic Acid n-Heptacosanoic Acid 87 C Montanic acid n-Octacosanoic acid 506-48-9 Straight 28:0 91 C 4250-38-8 Straight 29:0 Nonacosanoic Acid n-Nonacosanoic Acid 91 C Melissic acid n-Triacontanoic acid 506-50-3 Straight 30:0 93 C 38232-01-8 Straight 31:0 n-Hentriacontanoic Acid n-Dotriacontanoic Acid Straight 32:0 Lacceroic Acid Ceromelissic Acid n-Tritriacontanoic acid Straight 33:0 Geddic Acid n-Tetratriacontanoic acid Straight 34:0 Ceroplastic Acid n-Pentatriacontanoic acid Straight 35:0 SALES SPECIFICATION PALM OIL ACID (HARDENED) APPEARANCE Bead IODINE VALUE 0.5 max ACID VALUE 208 - 210 SAP VALUE 209 - 211 TITER 54 - 56 C COLOR 0.5 R / 2.5 Y CARBON DISTRIBUTION C14 (1% max) + C16 (62% max) + C18 (45% max) TRANSPORTATION PACKING 25kgs in bag , 17mts in Container HAZARD CLASS Not regulated UN NO. GENERAL DESCRIPTION OF FAT Commercial fats produced by organic processes in plants are palm, coconut, palm kernel, sunflower, soybean, and other oils. Their main components are triolein and triglyceryl esters of stearic (C18), palmitic (C16), myristic(C14), lauric (C12), oleic (C18:1), and other fatty acids. Tallow is a refined hard fat extracted from fatty deposits of animals, especially from suet (fatty tissues around the kidneys of cattle and sheep). The molecules of most natural fatty acids have an even number of carbon chains due to the linkage together by ester units. Analogous compounds of odd numbers carbon chain fatty acids can be made synthetically. All fats are insoluble in water and have lighter weight than water. Industrial fats can be sub-classified as fat, grease or oil depending on melting point. Fats that are liquid at room temperature are referred to oil. Grease has a higher initial viscosity than oil. It is used as a lubricant. The organic processes to convert fats to fatty acids (or esters) and glycerol is called oleochemistry. Fatty acids and glycerol are produced by hydrolysis (addition reaction of water molecule with cleavage of parent molecules) of the triglycerides. Fatty esters are produced by esterification reaction. Coconut or palm oils are better source to get saturated fatty acids than sunflower, soybean or rapeseed oils which have more unsaturated fatty acids composition of triglycerides. Tall oil fatty acid (TOFA) is a low cost unsaturated fatty acid (oleic acid) and is a source of low boiling point fatty acids. It is an alternative to tallow fatty acid in soap applications. Generally, commercial coconut fatty acid has carbon chain composition of; C10 (5% max) + C12 (45 - 55%) + C14 (20 - 25%) + C16 (10 - 15 %) + C18 (10 - 15% max, including unsaturated fatty acids). Fats are used to make soap, food products, cosmetics, and candles, and lubricants. They are wisely used in producing synthetic surfactants. PRICE INFORMATION Please contact us at [email protected] .
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