71718
Sodium L-lactate
≥99.0% (NT)
Synonym(s):
(S)-2-Hydroxypropionic acid sodium salt, L-Lactic acid sodium salt, Sarcolactic acid sodium salt
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About This Item
Empirical Formula (Hill Notation):
C3H5NaO3
CAS Number:
Molecular Weight:
112.06
UNSPSC Code:
12352001
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-762-3
Beilstein/REAXYS Number:
4567087
MDL number:
Assay:
≥99.0% (NT)
Form:
solid
Quality Level
assay
≥99.0% (NT)
form
solid
optical activity
[α]20/D −12.5±0.5°, c = 1% in H2O
optical purity
enantiomeric ratio: ≥97.0 (enzymatic)
feature
chiral
impurities
≤1% water
mp
163-165 °C (lit.)
functional group
hydroxyl
storage temp.
2-8°C
SMILES string
[Na+].C[C@H](O)C([O-])=O
InChI
1S/C3H6O3.Na/c1-2(4)3(5)6;/h2,4H,1H3,(H,5,6);/q;+1/p-1/t2-;/m0./s1
InChI key
NGSFWBMYFKHRBD-DKWTVANSSA-M
General description
Sodium L-lactate is the sodium salt of L-lactic acid and is widely utilized as a chiral building block in organic synthesis for the preparation of various chiral compounds. It can also be used as a mild reducing agent in synthetic chemistry applications.
Application
Sodium L-lactate can be used as a:
- Reagent for the dissolution of calcium D-gluconate.
- Crystallizing agent in the synthesis of Sn-containing silicate catalysts.
- Chiral building block to prepare chiral pyrrolidine intermediate, which is further used to synthesize chiral pyrrolidinium ionic liquids.
- Mild reducing agent in the selective reduction of CuO into Cu nanorods.
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Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Clinical evaluation of sodium bicarbonate, sodium L-lactate, and sodium acetate for the treatment of acidosis in diarrheic calves.
Kasari TR
Journal of the American Veterinary Medical Association, 187(4), 392-397 (1985)
Michael G Tordoff et al.
Chemical senses, 39(6), 515-528 (2014-05-23)
Genetic ablation of calcium homeostasis modulator 1 (CALHM1), which releases adenosine triphosphate from Type 2 taste cells, severely compromises the behavioral and electrophysiological responses to tastes detected by G protein-coupled receptors, such as sweet and bitter. However, the contribution of
Lucy Liu et al.
Cell metabolism, 26(5), 719-737 (2017-10-03)
Elevated reactive oxygen species (ROS) induce the formation of lipids in neurons that are transferred to glia, where they form lipid droplets (LDs). We show that glial and neuronal monocarboxylate transporters (MCTs), fatty acid transport proteins (FATPs), and apolipoproteins are
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 71718-10G | 04061832851129 |
| 71718-1KG | 04061826680728 |
| 71718-50G | 04061835289103 |