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

3-methoxycatechol
1,2-benzenediol, 3-methoxy-

Supplier Sponsors

CAS Number: 934-00-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:213-276-4
FDA UNII: IC13U5393C
Nikkaji Web:J107.379F
Beilstein Number:1909165
MDL:MFCD00002191
XlogP3:0.80 (est)
Molecular Weight:140.13836000
Formula:C7 H8 O3
BioActivity Summary:listing
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
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Appearance:pink to brown crystalline solid (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 42.80 °C. @ 760.00 mm Hg
Boiling Point: 268.00 to 269.00 °C. @ 760.00 mm Hg (est)
Boiling Point: 146.00 to 147.00 °C. @ 15.00 mm Hg
Vapor Pressure:0.005000 mmHg @ 25.00 °C. (est)
Flash Point: 247.00 °F. TCC ( 119.50 °C. ) (est)
logP (o/w): 0.937 (est)
Soluble in:
 alcohol
 water, 1.549e+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.
3-Methoxycatechol
Penta International
3-METHOXYCATECHOL
Santa Cruz Biotechnology
For experimental / research use only.
3-Methoxycatechol
Sigma-Aldrich: Aldrich
For experimental / research use only.
3-Methoxycatechol 99%
TCI AMERICA
For experimental / research use only.
3-Methoxycatechol
 
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-methoxycatechol usage levels up to:
 not for fragrance use.
 
Recommendation for 3-methoxycatechol flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
Carcinogenic Potency Database:Search
EPA Substance Registry Services (TSCA):934-00-9
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :13622
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
3-methoxybenzene-1,2-diol
Chemidplus:0000934009
RTECS:CZ9002750 for cas# 934-00-9
 
References:
 3-methoxybenzene-1,2-diol
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:934-00-9
Pubchem (cid):13622
Pubchem (sid):134981412
 
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
CHEMBL:View
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2909.30.6000
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
 wood smoke
Search Picture
 
Synonyms:
1,2-benzenediol, 3-methoxy-
 catechol, 3-methoxy-
1,2-dihydroxy-3-methoxybenzene
2,3-dihydroxyanisole
3-methoxy-1, 2-benzenediol
3-methoxy-1,2-benzene diol
3-methoxy-1,2-benzenediol
3-methoxybenzene-1,2-diol
3-methoxypyrocatechol
3-(methyloxy)benzene-1,2-diol
 pyrocatechol, 3-methoxy-
 pyrogallol 1-methyl ether
 pyrogallol 1-monomethyl ether
 

Articles:

PubMed:Hot-Hole Extraction from Quantum Dot to Molecular Adsorbate.
PubMed:The effect of substituents on the surface modification of anatase nanoparticles with catecholate-type ligands: a combined DFT and experimental study.
PubMed:High-throughput, high-content screening for novel pigmentation regulators using a keratinocyte/melanocyte co-culture system.
PubMed:The Three Catecholics Benserazide, Catechol and Pyrogallol are GPR35 Agonists.
PubMed:Biological clues to potent DNA-damaging activities in food and flavoring.
PubMed:Prediction model based on decision tree analysis for laccase mediators.
PubMed:Selective lignin and polysaccharide removal in natural fungal decay of wood as evidenced by in situ structural analyses.
PubMed:A previously uncultured, paper mill Propionibacterium is able to degrade O-aryl alkyl ethers and various aromatic hydrocarbons.
PubMed:A novel catechol-based universal support for oligonucleotide synthesis.
PubMed:Alanine 101 and alanine 110 of the alpha subunit of Pseudomonas stutzeri OX1 toluene-o-xylene monooxygenase influence the regiospecific oxidation of aromatics.
PubMed:Altering toluene 4-monooxygenase by active-site engineering for the synthesis of 3-methoxycatechol, methoxyhydroquinone, and methylhydroquinone.
PubMed:Quantitative structure toxicity relationships for catechols in isolated rat hepatocytes.
PubMed:Transglycosylation by Streptococcus mutans GS-5 glucosyltransferase-D: acceptor specificity and engineering of reaction conditions.
PubMed:Evidence for demethylation of syringyl moieties in archaeological wood using pyrolysis-gas chromatography/mass spectrometry.
PubMed:Effects of combined treatment with phenolic compounds and sodium nitrite on two-stage carcinogenesis and cell proliferation in the rat stomach.
PubMed:Effects of sodium nitrite and catechol, 3-methoxycatechol, or butylated hydroxyanisole in combination in a rat multiorgan carcinogenesis model.
PubMed:Effects of sodium nitrite and catechol or 3-methoxycatechol in combination on rat stomach epithelium.
PubMed:Formation of direct-acting genotoxic substances in nitrosated smoked fish and meat products: identification of simple phenolic precursors and phenyldiazonium ions as reactive products.
PubMed:Extraction-spectrophotometric determination of boron with 4,6-Di-tert-butyl-3-methoxycatechol and ethyl violet.
PubMed:Profiling of uremic ultrafiltrate using high resolution gas chromatography-mass spectrometry - identification of 6 polyphenols.
PubMed:Extradiol cleavage of 3-substituted catechols by an intradiol dioxygenase, pyrocatechase, from a Pseudomonad.
 
Notes:
None found
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