EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

3,4,5-trimethoxyphenol
phenol, 3,4,5-trimethoxy-

Supplier Sponsors

CAS Number: 642-71-7Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:211-387-2
FDA UNII: Search
Nikkaji Web:J107.381H
MDL:MFCD00008389
XlogP3-AA:0.50 (est)
Molecular Weight:184.19144000
Formula:C9 H12 O4
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
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Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in:
 water, 2.667e+004 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
Antiarol >98%
Odor: characteristic
Use: 3,4,5-Trimethoxyphenol is a natural flavonoid compound with potential antioxidant activity against peroxyl radicals found in the herbs of Callicarpa arborea, it is a useful synthetic intermediate in the synthesis of Thymonin. anti-oxidant
Santa Cruz Biotechnology
For experimental / research use only.
3,4,5-Trimethoxyphenol
Sigma-Aldrich: Aldrich
For experimental / research use only.
3,4,5-Trimethoxyphenol 97%
sds
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
natural substances and extractives
Recommendation for 3,4,5-trimethoxyphenol usage levels up to:
 not for fragrance use.
 
Recommendation for 3,4,5-trimethoxyphenol flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :69505
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
3,4,5-trimethoxyphenol
Chemidplus:0000642717
 
References:
 3,4,5-trimethoxyphenol
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):69505
Pubchem (sid):135026901
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEBI:View
CHEMBL:View
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2909.50.4500
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 buckwheat
Search Trop Picture
 
Synonyms:
 phenol, 3,4,5-trimethoxy-
 

Articles:

PubMed:Antibacterial and Anti-Quorum Sensing Molecular Composition Derived from Quercus cortex (Oak bark) Extract.
PubMed:Acyl glycosides with rare β-D-apiofuranosyl-β-D-glucopyranosyl-β-D-apiofuranosyl from Erycibe hainanesis.
PubMed:[Chemical constituents of Rhododendron seniavinii].
PubMed:Iridoid and phenolic glycosides from the roots of Prismatomeris connata.
PubMed:Shamiminol: a new aromatic glycoside from the stem bark of Bombax ceiba.
PubMed:On the way to understand antioxidants: chromanol and dimethoxyphenols gas-phase acidities.
PubMed:Three new flavonoid glycosides, byzantionoside B 6'-O-sulfate and xyloglucoside of (Z)-hex-3-en-1-ol from Ruellia patula.
PubMed:Antimalarial constituents from Nauclea orientalis (L.) L.
PubMed:Synthesis of a capillarisin sulfur-analogue possessing aldose reductase inhibitory activity by selective isopropylation.
PubMed:Synthesis and anticancer activities of 5,6,7-trimethylbaicalein derivatives.
PubMed:Constituents from the bark of Tabebuia impetiginosa.
PubMed:Lipid peroxidation inhibitory activity of some constituents isolated from the stem bark of Eucalyptus globulus.
PubMed:Aporphinoid alkaloids and other constituents from Lettowianthus stellatus.
PubMed:Synthesis and X-ray structure of 2-(3-methyl-2-butenyl)-3,4,5-trimethoxyphenol: a potent anti-invasive agent against solid tumours.
PubMed:Studies on the constituents of Ailanthus integrifolia.
 
Notes:
None found
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