1,2,4-trimethoxybenzene
hydroxyhydroquinone trimethyl ether
Identification
| Name | 1,2,4-trimethoxybenzene |
| IUPAC | 1,2,4-trimethoxybenzene |
| CAS Number | 135-77-3 |
| EINECS | 205-219-7 |
| FDA UNII | 3KU3WD07SS |
| Molecular Formula | C9 H12 O3 |
| Molecular Weight | 168.19224000 |
| MDL Number | MFCD00008360 |
| Nikkaji Number | J141.476C |
| Beilstein | 2047579 |
| XlogP3 | 2.10 (est) |
Regulatory
Physical Properties
| Appearance | colorless to pale yellow clear liquid (est) |
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Specific Gravity | 1.13000 to 1.13500 @ 20.00 °C. |
| Pounds per Gallon - (est). | 9.414 to 9.455 |
| Refractive Index | 1.53200 to 1.53400 @ 20.00 °C. |
| Boiling Point | 99.00 to 100.00 °C. @ 0.20 mm Hg, 247.00 to 248.00 °C. @ 760.00 mm Hg (est) |
| Vapor Pressure | 0.041000 mmHg @ 25.00 °C. (est) |
| Flash Point | 172.00 °F. TCC ( 77.90 °C. ) (est) |
| logP (o/w) | 1.640 (est) |
| Soluble in | alcohol |
| Insoluble in | water |
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 1,2,4-trimethoxybenzene usage levels up to | not for fragrance use. |
| Recommendation for 1,2,4-trimethoxybenzene flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
1,2,4-
benzene triol trimethyl ether
benzene, 1,2,4-trimethoxy-
hydroxyhydroquinone trimethyl ether
trimethoxy-1,2,4-benzene
PubMed:
[Chemical constituents from acetyl acetate extract fraction of Incarvillea delavayi].
PubMed:
Analysis of biogenic volatile organic compounds in zucchini flowers: identification of scent sources.
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The study of fingerprint characteristics of Dayi Pu-Erh tea using a fully automatic HS-SPME/GC-MS and combined chemometrics method.
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Identification of a potent xanthine oxidase inhibitor from oxidation of caffeic acid.
PubMed:
Trifluoromethanesulfonic acid catalyzed friedel-Crafts alkylations of 1,2,4-trimethoxybenzene with aldehydes or benzylic alcohols.
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Immunotoxicity activity of 1,2,4-trimethoxybenzene from the Paulownia coreana Uyeki. against Aedes aegypti L.
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[Chemical constituents from acetyl acetate extract fraction of Incarvillea delavayi].
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An efficient formal synthesis of the human telomerase inhibitor (+/-)-gamma-rubromycin.
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Indole as an olfactory synergist for volatile kairomones for diabroticite beetles.
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Iodide as the mediator for the reductive reactions of peroxidases.