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Safety Information

F4004

Sigma-Aldrich

β-Fluoropyruvic acid sodium salt monohydrate

≥98%

Synonym(s):

sodium 3-fluoro-2-oxopropanoate hydrate

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About This Item

Linear Formula:
FCH2COCO2Na · H2O
CAS Number:
238754-68-2
Molecular Weight:
146.05
MDL number:
MFCD00149108
UNSPSC Code:
12352106
PubChem Substance ID:
24894800
NACRES:
NA.25

Quality Level

200

Assay

≥98%

storage temp.

−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

InChI key

HDSZBLZMLDQKRW-UHFFFAOYSA-M

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

F4004-5G:
F4004-100MG:
F4004-5G-PW:
F4004-1G:
F4004-1G-PW:
F4004-500MG:
F4004-VAR:
F4004-BULK:

Certificates of Analysis (COA)

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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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