T69000
3,4,5-Trimethoxybenzoic acid
ReagentPlus®, 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:
NACRES:
NA.22
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Quality Level
product line
ReagentPlus®
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
ReagentPlus is a registered 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
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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)
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.
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
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
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