116807
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:
Molecular Weight:
164.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-987-4
Beilstein/REAXYS Number:
2044322
MDL number:
Assay:
98%
Form:
solid
Quality Level
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
Related Categories
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
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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Thi Nhi-Cong Le et al.
Journal of basic microbiology, 50(3), 241-253 (2010-02-10)
A soil bacterium isolated from oil-polluted sand samples collected in the Saudi Arabian Desert has been determined as Nocardia cyriacigeorgica, which has a high capacity of degrading and utilizing a broad range of hydrocarbons. The metabolic pathways of three classes
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
K G Moorhouse et al.
Biochemical pharmacology, 41(8), 1179-1185 (1991-04-15)
The formation of neutral lipophilic metabolites from five xenobiotic carboxylic acids was studied in isolated rat hepatocytes. Oleic acid was used as a positive control. Rates of formation of lipids lay in the order: oleic acid greater than phytanic acid
K R Ki et al.
Journal of chromatography. A, 891(2), 257-266 (2000-10-24)
The simultaneous enantiomeric separation of 30 racemic acids including 24 hydroxy acids in a single analysis is described for the determination of their absolute configurations. It involves the conversion of each enantiomer into diastereomeric O-trifluoroacetylated (-)-menthyl ester for the direct
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 116807-5G | 04061836673758 |
| 116807-25G | 04061836682002 |
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