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:
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 Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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
[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)
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