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Merck
CN

T81205

Sigma-Aldrich

三苯基乙酸

99%

别名:

三苯乙酸

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About This Item

线性分子式:
(C6H5)3CCO2H
CAS号:
分子量:
288.34
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

99%

mp

270-273 °C (lit.)

SMILES字符串

OC(=O)C(c1ccccc1)(c2ccccc2)c3ccccc3

InChI

1S/C20H16O2/c21-19(22)20(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H,(H,21,22)

InChI key

DCYGAPKNVCQNOE-UHFFFAOYSA-N

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危险声明

危险分类

Aquatic Chronic 4

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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分析证书(COA)

Lot/Batch Number

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S Fournel et al.
Biochimica et biophysica acta, 883(2), 190-196 (1986-09-04)
Bilirubin UDPglucuronosyltransferase of rat or human liver microsomes was inhibited, in vitro, by triphenylacetic acid and by structurally related arylcarboxylic acids. This inhibition appeared to be competitive towards bilirubin, and mixed-type towards UDPglucuronic acid. A decrease in the number of
A D Blackwood et al.
Biochimica et biophysica acta, 1206(2), 161-165 (1994-06-12)
Combinations of triisooctylamine with its hydrochloride, or of triphenylacetic acid with its Na+ salt, can function as buffers for use during biocatalysis in organic media. They can control the pH of an adjacent aqueous phase, even though both forms of
Grant A McNaughton-Smith et al.
Journal of medicinal chemistry, 51(4), 976-982 (2008-02-01)
Sickle cell disease (SCD) is a hereditary condition characterized by deformation of red blood cells (RBCs). This phenomenon is due to the presence of abnormal hemoglobin that polymerizes upon deoxygenation. This effect is exacerbated when dehydrated RBCs experience a loss

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