71718

Sodium L-lactate

≥99.0% (NT)

• Synonym(s): (S)-2-Hydroxypropionic acid sodium salt, L-Lactic acid sodium salt, Sarcolactic acid sodium salt
• Empirical Formula (Hill Notation): C₃H₅NaO₃
• CAS Number: 867-56-1
• Molecular Weight: 112.06
• Beilstein/REAXYS Number: 4567087
• EC Number: 212-762-3
• MDL number: MFCD00066576
• UNSPSC Code: 12352001
• PubChem Substance ID: 57652343
• NACRES: NA.22

Properties

• Quality Level: 200
• 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

Description

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.

Safety Information

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 1
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)