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Merck
CN

54960

Sodium 2-hydroxybutyrate

purum, ≥95.0% (NT)

Synonym(s):

(±)-2-Hydroxybutanoic acid sodium salt, 2-Hydroxybutyric acid sodium salt

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About This Item

Linear Formula:
CH3CH2CH(OH)COONa
CAS Number:
Molecular Weight:
126.09
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
225-812-4
MDL number:
Beilstein/REAXYS Number:
4825104
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grade

purum

assay

≥95.0% (NT)

SMILES string

[Na+].CCC(O)C([O-])=O

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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[Methionine malabsorption syndrome].
T Bamba et al.
Ryoikibetsu shokogun shirizu, (19 Pt 2)(19 Pt 2), 576-577 (1998-06-30)
I A Tarakanov et al.
Rossiiskii fiziologicheskii zhurnal imeni I.M. Sechenova, 84(4), 300-308 (1998-09-22)
Effects of alpha-hydroxybutyrate (GHB) involved a decrease in the respiration rate and subsequent periodic breathing in anesthetised cats and rats. No considerable changes occurred in systemic circulation. There were, however, some differences between the species in the patterns of respiratory
Carl J Yeoman et al.
PloS one, 8(2), e56111-e56111 (2013-02-14)
Bacterial vaginosis (BV) is the most common vaginal disorder of reproductive-age women. Yet the cause of BV has not been established. To uncover key determinants of BV, we employed a multi-omic, systems-biology approach, including both deep 16S rRNA gene-based sequencing
Iola F Duarte et al.
NMR in biomedicine, 20(4), 401-412 (2006-12-07)
This paper reports the first application of high-resolution (1)H NMR spectroscopy to the plasma of five juveniles with glycogen storage disease type 1a (GSD1a), permitting the characterisation of the plasma metabolic profile and the identification of alterations relative to a
Ferhan Siddiqi et al.
Biochemistry, 44(25), 9013-9021 (2005-06-22)
Mandelate racemase (MR, EC 5.1.2.2) from Pseudomonas putida catalyzes the Mg(2+)-dependent 1,1-proton transfer that interconverts the enantiomers of mandelate. Crystal structures of MR reveal that the phenyl group of all ground-state ligands is located within a hydrophobic cavity, remote from

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