K0875
Sodium 2-oxobutyrate
powder
Synonym(s):
2-Oxobutanoic acid sodium salt, 2-Oxobutyric acid sodium salt, Sodium α-ketobutyrate
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About This Item
Linear Formula:
CH3CH2COCOONa
CAS Number:
Molecular Weight:
124.07
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-937-8
Beilstein/REAXYS Number:
3631701
MDL number:
Assay:
≥97%
Form:
powder
Product Name
Sodium 2-oxobutyrate, powder
InChI key
SUAMAHKUSIHRMR-UHFFFAOYSA-M
InChI
1S/C4H6O3.Na/c1-2-3(5)4(6)7;/h2H2,1H3,(H,6,7);/q;+1/p-1
SMILES string
[Na+].CCC(=O)C([O-])=O
assay
≥97%
form
powder
color
white
mp
210 °C
storage temp.
2-8°C
Quality Level
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Application
Sodium 2-oxobutyrate can be used in the preparation of metal complexes such as lanthanide poly(imino carboxylate) complexes and half-sandwich complexes of (S)-1-amino-2-(methoxymethyl)-pyrrolidine. It can also be used in the synthesis of antiviral agents, 6-azapyrimidine-2′-deoxy-4′-thionucleosides.
Substrate for the determination of lactate dehydrogenase isoenzymes.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Formation of oligomeric lanthanide complexes with new tripodal poly (imino carboxylate) ligands.
Blake A J, et al.
J. Chem. Soc., Dalton Trans., 20, 3655-3658 (1997)
6-Azapyrimidine-2`-deoxy-4`-thionucleosides: Antiviral Agents against TK+ and TK? HSV and VZV Strains.
Maslen H L, et al.
Journal of Medicinal Chemistry, 47(22), 5482-5491 (2004)
Half-sandwich complexes of (S)-1-amino-2-(methoxymethyl)-pyrrolidine (SAMP).
Hoffmuller W, et al.
Journal of Organometallic Chemistry, 564(1), 179-187 (1998)
Hsien-Chung Tseng et al.
Microbial cell factories, 9, 96-96 (2010-11-30)
The ability to synthesize chiral building block molecules with high optical purity is of considerable importance to the fine chemical and pharmaceutical industries. Production of one such compound, 3-hydroxyvalerate (3HV), has previously been studied with respect to the in vivo
Hongbo Ling et al.
Biochemical and biophysical research communications, 361(1), 196-201 (2007-07-31)
Nikkomycins are peptidyl nucleoside antibiotics with potent activities against phytopathogenic and human pathogenic fungi. The sanM and sanN genes are required for the nikkomycin biosynthesis of Streptomyces ansochromogenes. In the present study, interaction between SanM and SanN was identified by
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