71716
Sodium D-lactate
≥99.0% (NT)
동의어(들):
(R)-2-Hydroxypropionic acid sodium salt, D-Lactic acid sodium salt
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보기 변경
제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
C3H5NaO3
CAS 번호:
Molecular Weight:
112.06
UNSPSC Code:
12352001
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5454721
Assay:
≥99.0% (NT)
Form:
powder
Quality Level
assay
≥99.0% (NT)
form
powder
optical activity
[α]20/D +12.5±0.5°, c = 1% in H2O
optical purity
enantiomeric ratio: ≥99:1 (enzymatic)
functional group
hydroxyl
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-;/m1./s1
InChI key
NGSFWBMYFKHRBD-HSHFZTNMSA-M
General description
Sodium D-lactate is the sodium salt of D-lactic acid. It is formed as an intermediate during the carbohydrate metabolism in muscle and liver.
저장 등급
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Xiaoxia Zhang et al.
Journal of industrial microbiology & biotechnology, 46(7), 899-909 (2019-04-10)
Lactoyl-CoA is critical for the biosynthesis of biodegradable and biocompatible lactate-based copolymers, which have wide applications. However, reports on acetyl-CoA: lactate CoA-transferases (ALCTs) are rare. To exploit novel ALCTs, amino acid sequence similarity searches based on the CoA-transferases from Clostridium
Joel Frandsen et al.
Scientific reports, 7(1), 5126-5126 (2017-07-13)
Oxidative stress is damaging to cells and contributes to aging and neurodegenerative disease. This state is mediated by production of imbalanced molecules, and reactive dicarbonyl compounds - mainly methylglyoxal. The glyoxalase pathway is an antioxidant defense system utilized to detoxify
Metabolism of Sodium d-Lactate: I. Utilization of Intravenously Injected Sodium d-Lactate by Normal Persons.
Soffer L J, et al.
Archives of Internal Medicine, 60(5), 876-881 (1937)