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Key Documents

V900577

Sigma-Aldrich

3,4,5-Trimethoxybenzoic acid

Vetec, reagent grade, 99%

Synonym(s):

Gallic acid trimethyl ether, Trimethylgallic acid

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About This Item

Linear Formula:
(CH3O)3C6H2CO2H
CAS Number:
Molecular Weight:
212.20
Beilstein/REAXYS Number:
884655
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

grade

reagent grade

product line

Vetec

assay

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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Legal Information

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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H Naviasky
Journal of pharmaceutical sciences, 73(4), 542-545 (1984-04-01)
An ion-pair column chromatographic/UV spectrophotometric method for assaying trimethobenzamide hydrochloride in capsules and injections is presented, as well as a method for the detection of 3,4,5- trimethoxybenzoic acid in trimethobenzamide hydrochloride bulk drug and dosage forms. Results obtained by the
E N Schachter et al.
Respiration; international review of thoracic diseases, 65(5), 393-400 (1998-10-23)
Latex manufacturing workers are exposed to a heterogeneous aerosol of organic compounds. Previous studies of latex workers involved in glove production indicate that these individuals are at risk of developing respiratory symptoms and impaired lung function. The effect of latex
M I Donnelly et al.
Journal of bacteriology, 142(3), 916-924 (1980-06-01)
When grown at the expense of 3,4,5-trimethoxybenzoic acid, a strain of Pseudomonas putida oxidized this compound and also 3,5-dimethoxy-4-hydroxybenzoic (syringic) and 3,4-dihydroxy-5-methoxybenzoic (3-O-methylgallic) acids; but other hydroxy- or methoxy-benzoic acids were oxidized slowly or not at all. Radioactivity appeared exclusively
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
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.

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