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T69000

Sigma-Aldrich

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:
118-41-2
Molecular Weight:
212.20
Beilstein:
884655
EC Number:
204-248-2
MDL number:
MFCD00002501
UNSPSC Code:
12352100
PubChem Substance ID:
24900412
NACRES:
NA.22

Quality Level

100

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
[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)
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
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