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Merck
CN

T69000

Sigma-Aldrich

3,4,5-三甲氧基苯甲酸

ReagentPlus®, 99%

别名:

五倍子酸三甲醚, 没食子酸三甲醚

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关于此项目

线性分子式:
(CH3O)3C6H2CO2H
CAS Number:
分子量:
212.20
Beilstein:
884655
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

产品线

ReagentPlus®

方案

99%

沸点

225-227 °C/10 mmHg (lit.)

mp

168-171 °C (lit.)

SMILES字符串

COc1cc(cc(OC)c1OC)C(O)=O

InChI

1S/C10H12O5/c1-13-7-4-6(10(11)12)5-8(14-2)9(7)15-3/h4-5H,1-3H3,(H,11,12)

InChI key

SJSOFNCYXJUNBT-UHFFFAOYSA-N

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法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

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

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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H Tateno et al.
Mutation research, 327(1-2), 237-246 (1995-03-01)
Many inhibitors of tubulin polymerization have a trimethoxybenzene ring in their molecules. Such trimethoxybenzoic compounds and their analogues may therefore have a potency to induce meiotic nondisjunction of oocytes. In this study, a single dose of reserpine (0.5 microgram/g body
S Kleis-San Francisco et al.
The Journal of experimental zoology, 244(1), 133-143 (1987-10-01)
In the amphibian ovarian follicle, progesterone production is thought to induce maturation of the enclosed oocyte. Intracellular mechanisms regulating these events in the somatic and germ cells are incompletely understood. However, calcium appears to play a role in the production
[Synthesis and the study of the effect of new 3,4,5-trimethoxybenzoic acid derivatives on the central nervous system].
R Glinka et al.
Acta poloniae pharmaceutica, 42(2), 117-122 (1985-01-01)
Yan-Jun Hu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 65(3-4), 988-992 (2006-05-09)
The interaction between 3,4,5-trimethoxybenzoic acid (TMBA) and bovine serum albumin (BSA) was studied by fluorescence and UV-vis absorption spectroscopy. In the mechanism discussion, it was proved that the fluorescence quenching of BSA by TMBA is a result of the formation
E Pogonowska-Wala
Polish journal of pharmacology and pharmacy, 33(3), 365-371 (1981-10-01)
Craviten hydrolysis in vitro was studied in human, rat and canine plasma and erythrocytes. Craviten was degraded during the incubation with plasma and the hydrolysis was inhibited by trimethoxybenzoic acid, a metabolite of Craviten. Erythrocyte enzymes do not participate in

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