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Merck
모든 사진(1)

주요 문서

T69000

Sigma-Aldrich

3,4,5-Trimethoxybenzoic acid

ReagentPlus®, 99%

동의어(들):

Gallic acid trimethyl ether, Trimethylgallic acid

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About This Item

Linear Formula:
(CH3O)3C6H2CO2H
CAS Number:
Molecular Weight:
212.20
Beilstein:
884655
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

제품 라인

ReagentPlus®

분석

99%

bp

225-227 °C/10 mmHg (lit.)

mp

168-171 °C (lit.)

SMILES string

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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관련 카테고리

법적 정보

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

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
Y Mimaki et al.
Bioscience, biotechnology, and biochemistry, 60(6), 1049-1050 (1996-06-01)
Bioassay-guided fractionation of the MeOH extract of Ornithogalum saundersiae bulbs led to the isolation of a new cholestane bisdesmoside with potent cytotoxic activities toward leukemia HL-60 and MOLT-4 cells. The structure was deduced mainly from spectroscopic information.
[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)
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
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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