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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1 EACH
¥376.36
About This Item
Empirical Formula (Hill Notation):
C3H5NaO3
CAS Number:
Molecular Weight:
112.06
Beilstein:
4567087
EC Number:
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.22
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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
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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.[1]
- Crystallizing agent in the synthesis of Sn-containing silicate catalysts. [2]
- 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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
Spontaneous supersaturation of calcium D-gluconate during isothermal dissolution of calcium L-lactate in aqueous sodium D-gluconate
Martina V et al,
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