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B34729

Sigma-Aldrich

Biphenyl-4-carboxylic acid

95%

Synonym(s):

4-Phenylbenzoic acid

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About This Item

Linear Formula:
C6H5C6H4CO2H
CAS Number:
Molecular Weight:
198.22
Beilstein:
973519
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

95%

form

crystals

mp

220-225 °C (lit.)

SMILES string

OC(=O)c1ccc(cc1)-c2ccccc2

InChI

1S/C13H10O2/c14-13(15)12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H,(H,14,15)

InChI key

NNJMFJSKMRYHSR-UHFFFAOYSA-N

Gene Information

human ... ALB(213) , BAD(572)

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Related Categories

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Daniil Naberezhnyi et al.
Physical chemistry chemical physics : PCCP, 22(17), 9808-9814 (2020-04-28)
Ionic liquids and nanoscale membranes are both considered as promising functional components to design next-generation gas separation technologies. Herein, we combine free-standing carbon nanomembranes (CNMs) with [bmim][Tf2N] ionic liquid having affinity to carbon dioxide, and explore molecular permeation through such
T Nanbo
Journal of pharmacobio-dynamics, 5(12), 988-993 (1982-12-01)
The mechanism responsible for the deconjugation of the glucuronide of p-phenyl benzoic acid (PPBA) in fetal intestine and amniotic fluid was studied in rats. Non-enzymatic hydrolysis of PPBA glucuronide in intestine was little before birth. The activity of beta-glucuronidase (beta-G)
T Nanbo
Journal of pharmacobio-dynamics, 5(11), 849-852 (1982-11-01)
The hepatic microsomal UDP-glucuronyltransferase (UDPGT) for p-phenyl benzoic acid (PPBA) in the developing fetus of rat was investigated. The kinetic properties of UDPGT in microsome of fetus changed during developmental period. The value of the Vmax for PPBA and uridine
T Nanbo
Toxicology and applied pharmacology, 92(3), 381-389 (1988-03-15)
A pharmacokinetic model of the maternal-fetal amniotic fluid system was designed to permit calculation of clearances from the steady-state concentrations of p-phenylbenzoic acid (PPBA) during infusion of PPBA into the maternal vein and the amniotic fluid of pregnant rats on
T Nanbo et al.
Chemico-biological interactions, 89(2-3), 169-182 (1993-12-01)
The inhibition of biphenylcarboxylic acid analogs on glyceride synthesis was studied in association with conformation of the chemicals. Chemicals used were benzoic acid substituted with phenyl, benzoyl and phenoxy groups, phenylphenyloxyacetic acid and p-phenylacetic acid. Twist angles were calculated by

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