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P31701

Sigma-Aldrich

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:
492-37-5
Molecular Weight:
150.17
Beilstein:
1863558
EC Number:
207-752-0
MDL number:
MFCD00002650
UNSPSC Code:
12352100
PubChem Substance ID:
24898400
NACRES:
NA.22

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

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

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

Certificates of Analysis (COA)

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D K Bhattacharyya et al.
The Journal of biological chemistry, 271(4), 2179-2184 (1996-01-26)
Examination of the crystal structure of the ovine prostaglandin endoperoxide synthase-1 (PGHS-1)/S- flurbiprofen complex (Picot, D., Loll, P.J., and Garavito, R.M. (1994) Nature 367, 243-2491) suggests (a) that the carboxyl group of arachidonic acid interacts with the arginino group of
Frédéric De Wael et al.
European journal of medicinal chemistry, 45(9), 3564-3574 (2010-06-24)
Based on the imidazo-[1,2-a]-pyrazin-3-(7H)-one scaffold, a dual action prodrug has been designed for combining antioxidant and anti-inflammatory activities, possibly unmasked upon oxidation. The construction of the target-molecule requires two building blocks, namely a 2-amino-1,4-pyrazine and a 2-ketoaldehyde. Attempts to synthesize
T Yamaguchi et al.
Drug metabolism and disposition: the biological fate of chemicals, 15(4), 535-539 (1987-07-01)
The contribution of the liver and kidney to the optical isomerization of (R)-(-)-2-phenylpropionic acid (hydratropic acid (HTA] was examined by iv injection of racemic HTA (20 mg/kg) to nephrectomized and bile duct-ligated rats (NEBL-rats), eviscerated rats with nonfunctioning livers (EVIS-rats)
David M Shackleford et al.
Current drug metabolism, 7(7), 817-826 (2006-11-01)
The vectorial movement of glucuronide conjugates from blood into bile can be an important elimination route for many drug metabolites, however the intrinsic hydrophilicity of those conjugates may conceptually act to reduce the overall efficiency of that process by limiting
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