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Merck

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號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

99%

mp

270-273 °C (lit.)

SMILES 字串

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 密鑰

DCYGAPKNVCQNOE-UHFFFAOYSA-N

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危險聲明

危險分類

Aquatic Chronic 4

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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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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