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P8001

Sigma-Aldrich

Sodium phenylpyruvate

powder

Synonym(s):

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

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About This Item

Linear Formula:
C6H5CH2COCOONa
CAS Number:
114-76-1
Molecular Weight:
186.14
Beilstein:
4770978
EC Number:
204-053-2
MDL number:
MFCD00002590
UNSPSC Code:
12352100
PubChem Substance ID:
57654561
NACRES:
NA.22

form

powder

Quality Level

200

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000402531
0000387128
0000402531
0000387128
0000288477

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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
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
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)
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]
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
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