Lactic Acid
KASEL Chemikals
Synonyms: 2-Hydroxypropanoic acid, alpha-Hydroxypropionic Acid, 1-Hydroxyethanecarboxylic acid, Ethylidenelactic acid, Milchsäure (German)
In solution, it can lose a proton from the acidic group, producing the lactate ion CH3CH(OH)COO−. It is miscible with water or ethanol, and is hygroscopic. Lactic acid does not exist as an acid in the body: it exists in another form called “lactate”, and it is this that is actually measured in the blood when “lactic acid” concentration is determined, as is done from time to time. This distinction is important not only for the sake of correctness, but more importantly, because lactate and lactic acid would have different physiological effects. Lactic acid is chiral and has two optical isomers. One is known as L-(+)-lactic acid or (S)-lactic acid and the other, its mirror image, is D-(-)-lactic acid or (R)-lactic acid. L-(+)-Lactic acid is the biologically important isomer. |
General information
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Chemical formula: C3H6O3 |
Specific Gravity: 1.2 |
Applications
Lactic acid is used in foods to add tartness and as a preservative. The name comes from the Latin word for milk, but most lactic acid is produced commercially from corn fermentation.
Lactic acid is what gives the sour taste to spoiled milk, and to sauerkraut.
Storge terms
Keep in a tightly closed container, stored in a cool, dry, ventilated area. Protect against physical damage. Isolate from any source of heat or ignition.
Specification
(Here you can download Specification as PDF-Files.)