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L+Lactic Acid, Calcium Salt, Hydrate
L+Lactic Acid, Calcium Salt, Hydrate
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| Lactic acid (2-hydroxypropanoic acid), also known as milk acid, is a chemical compound that plays a role in several biochemical processes. It was first isolated in 1780 by a Swedish chemist, Carl Wilhelm Scheele, and is a carboxylic acid with a chemical formula of C3H6O3. It has a hydroxyl group adjacent to the carboxyl group, making it an alpha hydroxy acid (AHA). 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 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. | | | Catalog # | L1017-03 | | Appearance | White to faint yellow powder | | Solubility (50mg/ml) | Colorless to pale yellow, clear, complete | | Tritration, Calcium (EDTA 0.1M) | 16.0-20.0% | | Water Content | ~0.1% | | Storage and Stability | Lyophilized powder may be stored at -20°C. Stable for 12 months at -20°C. Reconstitute with sterile ddH2O. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Reconstituted product is stable for 6 months at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer. | | CAS Number | 41372-22-9 | | Molecular Formula | C6H10O6•Ca•H2O | | Molecular Weight | 218.22 | | Purity (Enzymatic, Adjusted for H2O content) | ~90% (Adjusted for H2O content) | | | Important Note | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological. | | Alternate names | (S)-2-Hydroxypropionic acid, Calcium Salt; Calcium Lactate; Calcium-L-2-hydroxypropionate |
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