Sodium L-lactate, ~98%

Base Information

• Chemical Name: Sodium L-lactate, ~98%
• CAS No.: 867-56-1
• Molecular Formula: C3H6O3.Na
• Molecular Weight: 112.061
• Hs Code.: 29181100
• Mol file: 867-56-1.mol

Synonyms:Sodium L-lactate, ~98%;SCHEMBL377377;s6010;Sodium L-lactate, >=99.0% (NT);Sodium lactate, United States Pharmacopeia (USP) Reference Standard;Sodium L-lactate, Pharmaceutical Secondary Standard;Certified Reference Material

Chemical Property of Sodium L-lactate, ~98%

Chemical Property:

• Appearance/Colour: liquid
• Melting Point: 163-165 °C(lit.)
• Refractive Index: 1,422-1,425
• Boiling Point: 227.6 °C at 760 mmHg
• Flash Point: 109.9 °C
• PSA: 60.36000
• Density: 1.33 g/cm³
• LogP: -1.88290
• Storage Temp.: 2-8°C
• Sensitive.: Hygroscopic
• Solubility.: Aqueous Base (Sparingly), Water (Sparingly)
• Water Solubility.: soluble
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 113.02146333
• Heavy Atom Count: 7
• Complexity: 59.1

Purity/Quality:

99% ^*data from raw suppliers

L-LactIc Acid, Sodium Salt ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 24/25-36-26

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C(=O)O)O.[Na]
• Isomeric SMILES: C[C@@H](C(=O)O)O.[Na]
• Uses: Sodium L-lactate is used as a food additive, preservative, acidity regulator and bulking agent. It finds application in shampoo and liquid soaps and other related products. It acts as an effective humectant and moisturizer. It is used in the treatment of arrhythmias.

Technology Process of Sodium L-lactate, ~98%

There total 4 articles about Sodium L-lactate, ~98% which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 70.0%

sodium pyruvate (113-24-6) → sodium L-lactate (867-56-1)

Guidance literature:

enzymatic electrolysis;

DOI:10.1021/jo951408v

Reference yield: 51.71%

L-menthyl L-lactoyl L-lactate (923031-01-0) + L-menthyl L-lactoyl L-lactoyl L-lactate (923031-02-1) → (-)-menthol (2216-51-5) + sodium L-lactate (867-56-1) + (1R,2S,5R)-menthyl (S)-(-)-lactate (61597-98-6,185915-25-7)

Guidance literature:

With sodium hydroxide; water; In n-heptane; at 15 - 60 ℃; for 0.6 - 3.6h; pH=11.65 - 14; Product distribution / selectivity;

Reference yield:

serin (302-84-1,83245-15-2) → C3H6NO3(1-)*Na(1+) (246855-94-7) + sodium acetate (127-09-3) + sodium butyrate (156-54-7) + sodium L-lactate (867-56-1)

Guidance literature:

serin; at 37 ℃; for 48h; pH=7.3 - 7.4; Microbiological reaction; aq. phosphate buffer; Inert atmosphere;

With sodium hydroxide; pH=9.5; enantioselective reaction; aq. phosphate buffer;

DOI:10.1016/j.tetasy.2011.07.026

upstream raw materials:

sodium pyruvate

L-menthyl L-lactoyl L-lactate

L-menthyl L-lactoyl L-lactoyl L-lactate

serin

Downstream raw materials:

(S)-2-acetoxypropanoyl chloride

C₁₃H₁₂I₃NO₆

(S)-2-acetoxypropionic acid

sodium pyruvate

Refernces

• 1、 Poznansky, Barnabas,Reeve, Holly A.,Thompson, Lisa A.,Vincent, Kylie A.,Warren, Sarah A.. "Carbon as a Simple Support for Redox Biocatalysis in Continuous Flow". . p. 2281 - 2287. Retrieved 2020.
• 2、 Ramezani, Mohammad,White, Robert L.. "Enantioselective catabolism of racemic serine: Preparation of d-serine using whole cells of Fusobacterium nucleatum". experimental part. p. 1473 - 1478. Retrieved 2011/11/12.