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3,4,5-Trimethoxybenzoic acid, 99%|488231|118-41-2

3,4,5-Trimethoxybenzoic acid, 99%

Cat. No JK488231_100_G
J&K Chemical

Product Information

Product Name
3,4,5-Trimethoxybenzoic acid, 99%
Brand Name
J&K
Product Number
488231
CAS
118-41-2
Molecular Formula
C10H12O5
Molecular Weight
212.20
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
Gallic acid trimethyl ether
PubChem CID
8357
IUPAC Name
3,4,5-trimethoxybenzoic acid
InChI Key
SJSOFNCYXJUNBT-UHFFFAOYSA-N
SMILES
COC1=CC(=CC(=C1OC)OC)C(=O)O

Properties

Melting Point
168-171
Boiling Point
225-227

Safety Information

Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References

Effect of Solvents Polarity on Phytochemical Composition and Pharmacological Properties of Zygophyllum cornutum Coss.
Publication Name: Pharmaceutical Chemistry Journal
Publication Date: 2025-04
DOI: 10.1007/s11094-025-03365-5

Chemical profiling and mechanistic insights into the antibacterial efficacy of Melaleuca cajuputi leaf extract
Publication Name: BMC Complementary Medicine and Therapies
Publication Date: 2025-03-29
DOI: 10.1186/s12906-025-04790-5

Discovery of novel quinazoline derivatives containing trifluoromethyl against cell proliferation by targeting werner helicase
Publication Name: Molecular Diversity
Publication Date: 2025-03-28
DOI: 10.1007/s11030-025-11175-w

Diaryl Isoxazole Analog of Combretastatin A4 (A Promising Substance for an Antitumor Drug
Publication Name: Pharmaceutical Chemistry Journal
Publication Date: 2025-01
DOI: 10.1007/s11094-025-03297-0

Biotransformation of Compounds Catalyzed by Plant Cells, Hairy Roots and Enzymes
Publication Name: In Vitro Production of Plant Secondary Metabolites
Publication Date: 2025
DOI: 10.1007/978-981-97-8808-8_22

3,4,5-Trimethoxybenzoic acid, 99%

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