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P37602

5-Phenylvaleric acid

Name: 5-Phenylvaleric acid
Brand: ALDRICH

99%

Synonym(s):

5-Phenylpentanoic acid

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About This Item

Linear Formula:

C₆H₅CH₂CH₂CH₂CH₂COOH

CAS Number:

2270-20-4

Molecular Weight:

178.23

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24898447

EC Number:

218-872-8

Beilstein/REAXYS Number:

2049062

MDL number:

MFCD00004416

Assay:

99%

Form:

crystals

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Properties

assay

99%

form

crystals

bp

177-178 °C/13 mmHg (lit.)

mp

58-60 °C (lit.)

SMILES string

OC(=O)CCCCc1ccccc1

InChI

1S/C11H14O2/c12-11(13)9-5-4-8-10-6-2-1-3-7-10/h1-3,6-7H,4-5,8-9H2,(H,12,13)

InChI key

BYHDDXPKOZIZRV-UHFFFAOYSA-N

Description

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Intracellular degradation of two structurally different polyhydroxyalkanoic acids accumulated in Pseudomonas putida and Pseudomonas citronellolis from mixtures of octanoic acid and 5-phenylvaleric acid.

D M Chung et al.

International journal of biological macromolecules, 29(4-5), 243-250 (2001-11-24)

From a set of mixed carbon sources, 5-phenylvaleric acid (PV) and octanoic acid (OA), polyhydroxyalkanoic acid (PHA) was separately accumulated in the two pseudomonads Pseudomonas putida BM01 and Pseudomonas citronellolis (ATCC 13674) to investigate any structural difference between the two

Metabolism of dietary procyanidins in rats.

Marie-Paule Gonthier et al.

Free radical biology & medicine, 35(8), 837-844 (2003-10-15)

Procyanidins are major dietary polyphenols made of elementary flavan-3-ol (epi)catechin units. They have antioxidant properties and may contribute to health benefits in humans, but little is known about their metabolic fate. We compared here the metabolism of procyanidin dimer B3

Specificity of procaine and ester hydrolysis by human, minipig, and rat skin and liver.

Christopher Jewell et al.

Drug metabolism and disposition: the biological fate of chemicals, 35(11), 2015-2022 (2007-08-01)

The capacity of human, minipig, and rat skin and liver subcellular fractions to hydrolyze the anesthetic ester procaine was compared with carboxylesterase substrates 4-methylumbelliferyl-acetate, phenylvalerate, and para-nitrophenylacetate and the arylesterase substrate phenylacetate. Rates of procaine hydrolysis by minipig and human

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Global Trade Item Number

SKU	GTIN
P37602-25G	04061831827460