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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-248-2
Beilstein/REAXYS Number:
884655
MDL number:
Assay:
99%
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
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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)