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286958

Phenylpyruvic acid

98%

Synonym(s):

2-Oxo-3-phenylpropanoic acid, 2-Oxo-3-phenylpropionic acid

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$112.00

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$548.00

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About This Item

Linear Formula:
C6H5CH2COCOOH
CAS Number:
156-06-9
Molecular Weight:
164.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24857257
EC Number:
205-847-1
Beilstein/REAXYS Number:
2207312
MDL number:
MFCD00002589
Assay:
98%

Key Documents

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Quality Level

200

assay

98%

mp

150-154 °C (lit.)

functional group

carboxylic acid, ketone, phenyl

storage temp.

−20°C

SMILES string

OC(=O)C(=O)Cc1ccccc1

InChI

1S/C9H8O3/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5H,6H2,(H,11,12)

InChI key

BTNMPGBKDVTSJY-UHFFFAOYSA-N

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1 of 4

This Item
74346P7251376906
Phenylpyruvic acid 98%

Sigma-Aldrich

286958

Phenylpyruvic acid

Phenylpyruvic acid analytical standard

Supelco

74346

Phenylpyruvic acid

3-Phenyllactic acid ≥98%

Sigma-Aldrich

P7251

3-Phenyllactic acid

D-(+)-3-Phenyllactic acid 98%

Sigma-Aldrich

376906

D-(+)-3-Phenyllactic acid

assay

98%

assay

≥97.0% (HPLC), 97.0-103.0% (T)

assay

≥98%

assay

98%

Quality Level

200

Quality Level

100

Quality Level

200

Quality Level

100

storage temp.

−20°C

storage temp.

−20°C

storage temp.

-

storage temp.

-

mp

150-154 °C (lit.)

mp

150-154 °C (lit.)

mp

-

mp

122-124 °C (lit.)

functional group

carboxylic acid

functional group

-

functional group

-

functional group

carboxylic acid, hydroxyl, phenyl

General description

Phenylpyruvic acid reduces glucose-6-phosphate dehydrogenase activity without pre-incubation[1].

Application

Phenylpyruvic acid was used in the synthesis of 3-phenyllactic acid (PLA) by lactate dehydrogenase[2].

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN4004
BCCJ3718
BCBV9597
BCBL5546V
1451191V

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Shuhuai Yu et al.
Biotechnology letters, 36(3), 627-631 (2013-11-20)
3-Phenyllactic acid (PLA) is an antimicrobial compound with broad and effective antimicrobial activity against both bacteria and fungi. Enzymatic production of PLA can be carried out from phenylpyruvic acid by lactate dehydrogenase (LDH); however, the enzymatic reaction is accompanied by
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]
Faqing Tang et al.
Clinical biochemistry, 44(8-9), 711-718 (2011-03-16)
To search for markers of nasopharyngeal carcinoma (NPC) for diagnosis. Using gas chromatography and mass spectrometry, we evaluated 51 serum metabolites in 49 NPC, 37 throat cancer patients and 40 healthy controls. High metabolites were selected and confirmed in NPC
Hajer Ouertatani-Sakouhi et al.
Journal of biomolecular screening, 15(4), 347-358 (2010-03-17)
Macrophage migration inhibitory factor (MIF) is a major mediator of innate immunity and inflammation and presents a potential therapeutic target for various inflammatory, infectious, and autoimmune diseases, including cancer. Although a number of inhibitors have been identified and designed based
Valeriano Dal Cin et al.
The Plant cell, 23(7), 2738-2753 (2011-07-14)
Altering expression of transcription factors can be an effective means to coordinately modulate entire metabolic pathways in plants. It can also provide useful information concerning the identities of genes that constitute metabolic networks. Here, we used ectopic expression of a
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Global Trade Item Number

SKUGTIN
286958-25G04061826264881
286958-5G04061826264904

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