P31701
2-Phenylpropionic acid
97%
Synonym(s):
(±)-2-Phenylpropionic acid, (±)-Hydratropic acid
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About This Item
Linear Formula:
CH3CH(C6H5)CO2H
CAS Number:
Molecular Weight:
150.17
Beilstein:
1863558
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
refractive index
n20/D 1.522 (lit.)
bp
260-262 °C (lit.)
density
1.1 g/mL at 25 °C (lit.)
SMILES string
CC(C(O)=O)c1ccccc1
InChI
1S/C9H10O2/c1-7(9(10)11)8-5-3-2-4-6-8/h2-7H,1H3,(H,10,11)
InChI key
YPGCWEMNNLXISK-UHFFFAOYSA-N
Gene Information
human ... IL8RA(3577)
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Related Categories
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
298.4 °F
Flash Point(C)
148 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Optical isomerization of 2-phenylpropionic acid (hydratropic acid, HTA) was studied in the organs of male rat in vitro. (R)-(-)-HTA was not isomerized by rat liver homogenate even after the addition of CoA, ATP, and Mg2+ to the incubation mixture; however
Chunze Li et al.
Chemical research in toxicology, 15(11), 1480-1487 (2002-11-20)
A series of studies was conducted to investigate the potential of (R)- and (S)-2-phenylpropionic acid (2-PPA) to undergo enantioselective covalent binding to protein in freshly isolated rat hepatocytes and to determine whether such covalent binding is dependent on acyl glucuronidation
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The Journal of pharmacology and experimental therapeutics, 305(1), 250-256 (2003-03-22)
Two alternative metabolic pathways, acyl glucuronidation and acyl-CoA formation, are implicated in the generation of reactive acylating metabolites of carboxylic acids. Here, we describe studies that determine the relative importance of these two pathways in the metabolic activation of a
Chromatograms
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