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Key Documents

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T69000

Sigma-Aldrich

3,4,5-Trimethoxybenzoic acid

ReagentPlus®, 99%

Sinónimos:

Gallic acid trimethyl ether, Trimethylgallic acid

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About This Item

Fórmula lineal:
(CH3O)3C6H2CO2H
Número de CAS:
118-41-2
Peso molecular:
212.20
Beilstein/REAXYS Number:
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

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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Certificados de análisis (COA)

Lot/Batch Number
STBL2690
STBH8567
STBF0699V
STBD0215V
STBB8332V

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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
[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)
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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