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116807

Sigma-Aldrich

3-Phenylbutyric acid

98%

Synonym(s):

(±)-3-Phenylbutyric acid, (±)-β-Methylhydrocinnamic acid

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About This Item

Linear Formula:
CH3CH(C6H5)CH2COOH
CAS Number:
4593-90-2
Molecular Weight:
164.20
Beilstein:
2044322
EC Number:
224-987-4
MDL number:
MFCD00002725
UNSPSC Code:
12352100
PubChem Substance ID:
24847305
NACRES:
NA.22

Quality Level

100

Assay

98%

form

solid

bp

170-172 °C/20 mmHg (lit.)

mp

35-38 °C (lit.)

density

1.515 g/mL at 25 °C (lit.)

functional group

carboxylic acid
phenyl

SMILES string

CC(CC(O)=O)c1ccccc1

InChI

1S/C10H12O2/c1-8(7-10(11)12)9-5-3-2-4-6-9/h2-6,8H,7H2,1H3,(H,11,12)

InChI key

ZZEWMYILWXCRHZ-UHFFFAOYSA-N

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General description

3-Phenylbutyric acid is a metabolite of the oxidation of sec-octylbenzene.

Application

3-Phenylbutyric acid is used to isolate Rhodococcus rhodochrous PB1 from compost soil.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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
STBK1891
STBJ3904
STBH0619
STBH0614
STBG9179

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Helge Jochens et al.
Chembiochem : a European journal of chemical biology, 11(13), 1861-1866 (2010-08-04)
Simultaneous multiple site-saturation mutagenesis was performed at four active-site positions of an esterase from Pseudomonas fluorescens to improve its ability to convert 3-phenylbutyric acid esters (3-PBA) in an enantioselective manner. Based on an appropriate codon choice derived from a structural
F S Sariaslani et al.
Journal of bacteriology, 152(1), 411-421 (1982-10-01)
Pseudomonas sp. isolated by selective culture with 3-phenylbutyrate (3-PB) as the sole carbon source metabolized the compound through two different pathways by initial oxidation of the benzene ring and by initial oxidation of the side chain. During early exponential growth
P D Ross et al.
Biophysical journal, 71(4), 2144-2154 (1996-10-01)
Values of K, delta G(o), delta H(o), delta S(o) and delta C(po) for the binding reaction of small organic ligands forming 1:1 complexes with either alpha- or beta-cyclodextrin were obtained by titration calorimetry from 15 degrees C to 45 degrees
S Simoni et al.
Applied and environmental microbiology, 62(3), 749-755 (1996-03-01)
Rhodococcus rhodochrous PB1 was isolated from compost soil by selective culture with racemic 3-phenylbutyric acid as the sole carbon and energy source. Growth experiments with the single pure enantiomers as well as with the racemate showed that only one of
Eva Bandres et al.
International journal of cancer, 125(11), 2737-2743 (2009-06-13)
In the last years, microRNAs (miRNA) have emerged as new molecular players involved in carcinogenesis. Deregulation of miRNAs expression has been shown in different human cancer but the molecular mechanism underlying the alteration of miRNA expression is unknown. To identify
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