(R)-S-lactoylglutathione

Base Information

Chemical Name:(R)-S-lactoylglutathione
CAS No.:25138-66-3
Molecular Formula:C₁₃H₂₁N₃O₈S
Molecular Weight:379.391
Hs Code.:
Nikkaji Number:J524.698I
Wikidata:Q63395383
Metabolomics Workbench ID:37583
Mol file:25138-66-3.mol

Synonyms:S-D-lactoylglutathione;S-lactoylglutathione

Suppliers and Price of (R)-S-lactoylglutathione

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of (R)-S-lactoylglutathione

Chemical Property:

Vapor Pressure:4.55E-30mmHg at 25°C
Boiling Point:806.1°Cat760mmHg
Flash Point:441.3°C
PSA：221.42000
Density:1.472g/cm³
LogP:-1.01320
XLogP3:-4.6
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:12
Exact Mass:379.10493581
Heavy Atom Count:25
Complexity:527

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C(=O)SCC(C(=O)NCC(=O)O)NC(=O)CCC(C(=O)O)N)O
Isomeric SMILES:C[C@H](C(=O)SC[C@@H](C(=O)NCC(=O)O)NC(=O)CC[C@@H](C(=O)O)N)O

Technology Process of (R)-S-lactoylglutathione

There total 4 articles about (R)-S-lactoylglutathione 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:

: 85354-25-2,85354-26-3
2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(1-hydroxy-2-oxo-propylsulfanyl)-ethylcarbamoyl]-butyric acid

: 25138-66-3,41656-56-8
S-lactoyl glutathione

Guidance literature:: With glyoxalase I;
DOI:10.1021/ja00526a042

Reference yield:

: 70-18-8
glutathion

: 25138-66-3,41656-56-8
S-lactoyl glutathione

Guidance literature:: Multi-step reaction with 2 steps

2: glyoxalase I

With glyoxalase I;
DOI:10.1021/ja00526a042

Reference yield:

: 40055-98-9,121-24-4,87140-29-2
oxidized glutathione

: 78-98-8
2-oxopropanal

: 25138-66-3,41656-56-8
S-lactoyl glutathione

Guidance literature:: With glyoxalase I; egg albumin; diothiothreitol; Rate constant; multistep reaction: 1) phosphate buffer, water, 30 deg C; further reagents;
DOI:10.1021/ja00526a042