B34729
联苯-4-羧酸
95%
别名:
4-苯基苯甲酸
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线性分子式:
C6H5C6H4CO2H
化学文摘社编号:
分子量:
198.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-203-1
Beilstein/REAXYS Number:
973519
MDL number:
Assay:
95%
Form:
crystals
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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(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
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, 6(8), 565-570 (1983-08-01)
The developmental change of the intrinsic clearance (Clint) and the hepatic clearance (ClH) for the glucuronidated p-phenylbenzoic acid (PPBA) by uridine 5'-phosphoglucronic acid-glucuronyltransferase (UDPGT) in liver of rat fetus was investigated. The UDPGT activity was stimulated by 225% by Brij
T Nanbo
Journal of pharmacobio-dynamics, 5(4), 213-221 (1982-04-01)
The pharmacokinetics in maternal-fetal unit of 14C-p-phenyl benzoic acid was studied in intact and bile-duct-cannulated pregnant rats following the intravenous administration. The half life of the maternal blood level was shortened by bile duct-cannulation. However, the effect of bile duct-cannulation
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