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
Pricing and availability is not currently available.
Recommended Products
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
K Fukuda et al.
Cancer letters, 164(1), 7-13 (2001-02-13)
Costunolide, the predominant sesquiterpene lactone in Saussureae radix, has been reported to exhibit potent chemopreventive effects on carcinogenesis. Effects of costunolide on cellular activation induced by a tumor-promoting phorbol ester 12-O-tetradecanoylphorbol-13-acetate (TPA) were investigated using a reporter gene assay which
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
[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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