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Merck
CN

B34729

Sigma-Aldrich

联苯-4-羧酸

95%

别名:

4-苯基苯甲酸

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关于此项目

线性分子式:
C6H5C6H4CO2H
CAS Number:
分子量:
198.22
Beilstein:
973519
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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质量水平

方案

95%

表单

crystals

mp

220-225 °C (lit.)

SMILES字符串

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

基因信息

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

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象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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