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ETHYL 2-MERCAPTOACETATE | |||
PRODUCT IDENTIFICATION |
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CAS NO. | 623-51-8 |
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EINECS NO. | 210-800-3 | ||
FORMULA | HSCH2COOC2H5 | ||
MOL WT. | 120.17 | ||
H.S. CODE |
2930.90 | ||
TOXICITY |
Oral rat LD50: 178 mg/kg | ||
SYNONYMS | Ethyl Thioglycolate; Mercaptoacetic acid ethyl ester; | ||
Ethyl mercaptoacetate; Ethyl alpha-mercaptoacetate; Ethyl mercaptoacetic acid; Thioglycolic acid ethyl ester; | |||
SMILES |
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CLASSIFICATION |
THIOGLYCOLATE / |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE | clear liquid | ||
MELTING POINT |
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BOILING POINT | 157 C | ||
SPECIFIC GRAVITY | 1.1 | ||
SOLUBILITY IN WATER |
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pH | |||
VISCOSITY | |||
AUTOIGNITION |
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REFRACTIVE INDEX |
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NFPA RATINGS | |||
FLASH POINT | 47 C | ||
STABILITY | Stable under ordinary conditions | ||
GENERAL DESCRIPTION & APPLICATIONS |
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Glycolic acid
is the smallest alpha-hydroxy acid (AHA) which has a hydroxyl group on the carbon atom next to
the acid group. If the hydroxy group is on the second carbon next to the acid
group, it is called beta-hydroxy acid. Glycolic acid is a low mole weight
compound but has dual functionality of alcohol and
acid. Because of its small molecular weight and size, it has a better capability
to penetrate skin. AHA is used extensively in cosmetics. It is known that it
diminishes the lines on the skin and make skins look young by acting as a
humectant to absorb moisture in air and by exfoliating action to break the bonds
between dead skin cells, Pure glycolic acid is a white
crystals; decomposes about 78
C; very
soluble in water, alcohols, acetone, acetates; slightly soluble in ethyl ether;
sparingly soluble in hydrocarbon solvents; polymerization occurs above 50
C. Commercially, it is available in
crystal form as well as in aqueous solutions of various concentrations, usually
70 percent or less. Activating both the hydroxyl and
carboxylic acid group, glycolic acid has the property to form metal complexes
and can be used in cleaning applications and hard water dissolution. Aqueous solution
grade is mainly used fro this cleaning application.
Glycolic
acid is an useful intermediate in organic synthesis including
oxidation/reduction, esterification and formation of oligomers as well as long
chain polymerization. Glycolic acid is naturally found in sugar beets, cane sugar,
and unripe grapes. It is known that it diminishes the lines on the skin and make
skins look young. Synthetic glycolic acid and its derivatives are used
commercially in leather tanning and textile dyeing; as a flavouring agent and
preservative in food processing, water treatment industries; pH control; and chemical intermediates as well as in household,
industrial, electronics cleaning applications and cosmetics. They are also used
in emulsion polymers, solvents and ink and paint additive to improve flow properties
and impart gloss.
'Thio' is a chemical prefix indicates the replacement of an oxygen in an acid radical by sulfur with a negative valence of 2; meaning 'sulfur' derived from the Greek theion. In substitutive nomenclature their names are formed by adding '-thiol' as a suffix to the name of the parent compound. When -SH is not the principal group, the prefix 'mercapto-' is placed before the name of the parent compound to denote an unsubstituted -SH group. Thioglycolic acid, a simple sulfur group- chained carboxylic acid, is a clear liquid; melts at -16. c, boils at 96 C; soluble in water. It is an useful chemical intermediate in the chemical reactions such as addition, elimination and cyclization. Sulfur group will react with bases, acids, ketones and organic halogen compounds, whereas the carboxylic group will preferentially react In the presence of alcohols or amines. The applications of thioglycolic acid and its derivatives are wide in the fields of;
Thioglycolic acid, a simple sulfur group- chained carboxylic acid, is a clear liquid; melts at -16. c, boils at 96 C; soluble in water. It is an useful chemical intermediate in the chemical reactions such as addition, elimination and cyclization. Sulfur group will react with bases, acids, ketones and organic halogen compounds, whereas the carboxylic group will preferentially react In the presence of alcohols or amines. The applications of thioglycolic acid and its derivatives are wide in the fields of PVC stabilizers, down-hole acidizing, corrosion inhibition in the oil field industry, manufacturing of pharmaceuticals, agrochemicals and dyes, shrink-resistant treatment of wool, fabric dying, leather processing. Thioglycolates are used in cosmetic hair-care products especially permanent waving products as they weaken the keratin structure by the opening of the cystine disulfide linkages. In addition to hair-waving application, they are used as depilating agents to remove unwanted body hair. The break-down of disulfide bonds in the cortex by thioglycolates either rearranges (permanent waving) or entirely destroys (depilating) hair structure. As an antioxidant application in cosmetics, thioglycolates protect the product itself not the skin against oxidative reactions promoted by ultraviolet radiation or oxygen.
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SALES SPECIFICATION | |||
APPEARANCE |
Clear liquid | ||
ASSAY |
99.0% max | ||
SPECIFIC GRAVITY | 1.10 - 1.11 | ||
TRANSPORTATION | |||
PACKING | |||
HAZARD CLASS | 3 (Packing Group: III) | ||
UN NO. | 3071 | ||
PRICE |
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