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P8001

Sigma-Aldrich

Sodium phenylpyruvate

powder

Sinónimos:

2-Oxo-3-phenylpropanoic acid, Phenylpyruvic acid sodium salt

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About This Item

Fórmula lineal:
C6H5CH2COCOONa
Número de CAS:
114-76-1
Peso molecular:
186.14
Beilstein/REAXYS Number:
4770978
EC Number:
204-053-2
MDL number:
MFCD00002590
UNSPSC Code:
12352100
PubChem Substance ID:
57654561
NACRES:
NA.22

form

powder

color

white to off-white

mp

>300 °C (lit.)

storage temp.

2-8°C

SMILES string

[Na+].[O-]C(=O)C(=O)Cc1ccccc1

InChI

1S/C9H8O3.Na/c10-8(9(11)12)6-7-4-2-1-3-5-7;/h1-5H,6H2,(H,11,12);/q;+1/p-1

InChI key

MQGYVGKMCRDEAF-UHFFFAOYSA-M

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Jun Wang et al.
Frontiers in microbiology, 10, 2357-2357 (2019-11-05)
Endogenous hydrogen sulfide (H2S), which is primarily generated by 3-mercaptopyruvate sulfurtransferase (3-MST) in Escherichia coli (E. coli) under aerobic conditions, renders bacteria highly resistant to oxidative stress. However, the biosynthetic pathway and physiological role of this gas under anaerobic conditions
William M Moe et al.
Environmental science & technology, 52(16), 9311-9319 (2018-07-26)
In situ bioremediation practices that include subsurface addition of fermentable electron donors to stimulate reductive dechlorination by anaerobic bacteria have become widely employed to combat chlorinated solvent contamination in groundwater. At a contaminated site located near Baton Rouge, Louisiana (USA)
Cristiana M L Di Giuro et al.
PloS one, 8(7), e68932-e68932 (2013-08-13)
(S)-Hydroxymandelate synthase (Hms) is a nonheme Fe(II) dependent dioxygenase that catalyzes the oxidation of 4-hydroxyphenylpyruvate to (S)-4-hydroxymandelate by molecular oxygen. In this work, the substrate promiscuity of Hms is characterized in order to assess its potential for the biosynthesis of
Sumit Chakraborty et al.
Biochemistry, 47(12), 3800-3809 (2008-03-05)
Direct spectroscopic observation of thiamin diphosphate-bound intermediates was achieved on the enzyme benzaldehyde lyase, which carries out reversible and highly enantiospecific conversion of ( R)-benzoin to benzaldehyde. The key enamine intermediate could be observed at lambda max 393 nm in
Tapan Kanti Paine et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(21), 6073-6081 (2007-05-01)
Iron(II)-phenylpyruvate complexes of tetradentate tris(6-methyl-2-pyridylmethyl)amine (6-Me3-TPA) and tridentate benzyl bis(2-quinolinylmethyl)amine (Bn-BQA) were prepared to gain insight into C-C bond cleavage catalyzed by dioxygenase enzymes. The complexes we have prepared and characterized are [Fe(6-Me3-tpa)(prv)][BPh4] (1), [Fe2(6-Me3-tpa)2(pp)][(BPh4)2] (2), and [Fe2(6-Me3-tpa)2(2'-NO2-pp)][(BPh4)2] (3), [Fe(6-Me3-tpa)(pp-Me)][BPh4]
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