|
ETHYL LACTATE | ||
PRODUCT IDENTIFICATION |
||
CAS NO. | 97-64-3, 687-47-8 (L-form) |
|
EINECS NO. | 202-598-0 | |
FORMULA | C5H10O3 | |
MOL WT. | 118.13 | |
H.S. CODE |
2932.29 | |
TOXICITY |
||
SYNONYMS | Lactic acid ethyl ester; 2-Hydroxypropanoic acid, ethyl ester; | |
Ethyllactat (German); Lactato de etilo (Spanish); Lactate d'éthyle (French); | ||
SMILES |
|
|
CLASSIFICATION |
||
PHYSICAL AND CHEMICAL PROPERTIES |
||
PHYSICAL STATE | clear liquid to yellow liquid | |
MELTING POINT | -26 C | |
BOILING POINT | 151 - 155 C | |
SPECIFIC GRAVITY | 1.029 - 1.032 | |
SOLUBILITY IN WATER | Soluble ( soluble in Alcohol, paraffin oils) | |
pH | ||
VAPOR DENSITY |
4.07 | |
AUTOIGNITION | ||
REFRACTIVE INDEX |
1.410 - 1.420 | |
NFPA RATINGS | Health: 1; Flammability: 1; Reactivity: 0 | |
FLASH POINT | 46 C | |
STABILITY | Stable under ordinary conditions | |
GENERAL DESCRIPTION & APPLICATIONS |
||
Lactic acid (chemically, alpha or 2-Hydroxypropionic acid) takes roles in metabolic processes in the body; in red blood and in
skeletal muscle tissues as a product of glucose and glycogen metabolism. Lactic acid is an "alpha
hydroxy acid: 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. Lactic acid is converted
in vivo to pyruvic acid (an alpha keto acid) which occurs as an intermediate
product in carbohydrate and protein metabolism in the body. Lactic
acid occurs as two optical isomers since the central carbon atom is bound to
four different groups; a dextro and a levo form ( or an inactive racemic mixture
of the two); only the levo form takes part in animal metabolism. Lactic acid is
present in sour milk and dairy products such as cheese, yogurt, and koumiss,
leban, wines. Lactic acid causes tooth decay since lactic acid bacteria
operates in the mouth. Although it can be prepared by chemical synthesis,
production of lactic acid by fermentation of glucose and other sugar substances
in the presence of alkaline such as lime or calcium carbonate is a less
expensive method. The six-carbon glucose molecule is broken down to two
molecules of the three-carbon compounds (lactic acid), during this anaerobic
condition. Synthetic lactic acid is used commercially in tanning leather and
dyeing wool; as a flavouring agent and preservative in food processing and
carbonated beverages; and as a raw material in making plastics, solvents, inks,
and lacquers; as a catalyst in numerous chemical processes. Lactic Acid is
available as aqueous solutions of various concentrations, usually 22 - 85
percent (pure lactic acid is a colourless, crystalline substance.) Some examples
of lactates (salts or esters of lactic acid) are:
|
||
SALES SPECIFICATION | ||
APPEARANCE |
clear to yellow liquid | |
ESTER CONTENT |
98.0% min |
|
ACID VALUE |
1 max (mg KOH/g) |
|
MOISTURE |
0.2% max |
|
TRANSPORTATION | ||
PACKING | 200kgs in drum | |
HAZARD CLASS | ||
UN NO. | 1192 | |
OTHER INFORMATION | ||
Hazard Symbols: , Risk Phrases: 36/37/38, Safety Phrases: 26-37/39 |
|
|