|
Category: natural substances and extractives
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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:
Suppliers:
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:
References:
Other Information:
Potential Blenders and core components note
Potential Uses:
Occurrence (nature, food, other): note
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. |
|