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Safety Information

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

Quality Level

100

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

P31701-BULK:
P31701-10G:
P31701-5G:
P31701-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCS3610
MKCP1245
MKCG1641
MKBR0189V
MKBL2665V

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Lina Sagert et al.
eLife, 9 (2020-03-14)
Adaptive immunity vitally depends on major histocompatibility complex class I (MHC I) molecules loaded with peptides. Selective loading of peptides onto MHC I, referred to as peptide editing, is catalyzed by tapasin and the tapasin-related TAPBPR. An important catalytic role
Ekaterina Chernevskaya et al.
Critical care (London, England), 24(1), 312-312 (2020-06-10)
High serum levels of certain aromatic microbial metabolites (AMM) are associated with severity and mortality in critically ill patients. Omics-based studies suggest gut dysbiosis and reduced microbiome diversity in critical conditions. However, the landscape of gut microbial metabolites is still
Chunze Li et al.
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
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
Y Nakamura et al.
Drug metabolism and disposition: the biological fate of chemicals, 15(4), 529-534 (1987-07-01)
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
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