3-methoxycatechol
1,2-benzenediol, 3-methoxy-
Identification
| Name | 3-methoxycatechol |
| CAS Number | 934-00-9 |
| EINECS | 213-276-4 |
| FDA UNII | IC13U5393C |
| Molecular Formula | C7 H8 O3 |
| Molecular Weight | 140.13836000 |
| MDL Number | MFCD00002191 |
| Nikkaji Number | J107.379F |
| Beilstein | 1909165 |
| XlogP3 | 0.80 (est) |
Regulatory
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), 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 |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| 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. |
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Potential Uses
Natural Occurrence
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
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.