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Merck

F4004

Sigma-Aldrich

β-Fluor-Brenztraubensäure Natriumsalz

≥98%

Synonym(e):

sodium 3-fluoro-2-oxopropanoate hydrate

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About This Item

Lineare Formel:
FCH2COCO2Na · H2O
CAS-Nummer:
Molekulargewicht:
146.05
MDL-Nummer:
UNSPSC-Code:
12352106
PubChem Substanz-ID:
NACRES:
NA.25

Qualitätsniveau

Assay

≥98%

Lagertemp.

−20°C

SMILES String

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

InChI

1S/C3H3FO3.Na.H2O/c4-1-2(5)3(6)7;;/h1H2,(H,6,7);;1H2/q;+1;/p-1

InChIKey

HDSZBLZMLDQKRW-UHFFFAOYSA-M

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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R R Taylor et al.
FEMS microbiology letters, 115(2-3), 163-167 (1994-01-15)
In contrast to previously studied non-fermentative arginine-hydrolysing (F-/A+) Mycoplasma species, M. gallinarum cells suspended in a salts solution oxidised ethanol and L-lactic, pyruvic and 2-oxobutyric acids. The organic acids were additionally shown effectively to replace arginine as energy sources in
Cody W van Dijk et al.
The journal of physical chemistry. A, 116(16), 4082-4088 (2012-03-27)
The ground state rotational spectra of 2-fluoropyridine and 3-fluoropyridine have been investigated using both Fourier transform microwave (FTMW) and chirped pulse Fourier transform microwave (cp-FTMW) spectroscopies. In addition to the parent species, the spectra of the (13)C and (15)N singly
P Urban et al.
European journal of biochemistry, 144(2), 345-351 (1984-10-15)
It has been shown that reduced flavocytochrome b2 not only catalyzes reduction of bromopyruvate [P. Urban, P.M. Alliel and F. Lederer (1983) Eur. J. Biochem. 134, 275-281] but also transforms it into pyruvate in a reductive elimination process. The dehydrohalogenation
Fluoropyruvate: a potent inhibitor of the bacterial and the mammalian pyruvate dehydrogenase complex.
H Bisswanger
Biochemical and biophysical research communications, 95(2), 513-519 (1980-07-31)
E B Borthwick et al.
The Biochemical journal, 305 ( Pt 2), 521-524 (1995-01-15)
Simplified procedures for assaying and purifying dihydrodipicolinate synthase (EC 4.2.1.52), the first enzyme of the lysine biosynthetic pathway, have been developed and electrospray ionization m.s. has been used to observe the imine intermediate with pyruvate and to investigate the reaction

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