- 2,4,6-Trimethylphenol
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- $2.55 / 25KG
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2020-06-02
- CAS:527-60-6
- Min. Order: 1KG
- Purity: 99.50% IN STOCK
- Supply Ability: 2600 MT per month
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| 2,4,6-Trimethylphenol Basic information |
Product Name: | 2,4,6-Trimethylphenol | Synonyms: | 2,4,6-TRIMETHYLPHENOL, 1000MG, NEAT;2,4,6-TRIMETHYLPHENOL PESTANAL, 250 MG;2,4,6-TRIMETHYLPHENOL / MESITOL;Benzene, 2-hydroxy-1,3,5-trimethyl;2,4,6-Trimethylphenol,99%;Hydroxymesitylene
Mesitol;2-hydroxymesitylen;mesito | CAS: | 527-60-6 | MF: | C9H12O | MW: | 136.19 | EINECS: | 208-419-2 | Product Categories: | Aromatic Phenols;Building Blocks;C9 to C20+;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;Phenols | Mol File: | 527-60-6.mol | ![2,4,6-Trimethylphenol Structure](CAS/GIF/527-60-6.gif) |
| 2,4,6-Trimethylphenol Chemical Properties |
| 2,4,6-Trimethylphenol Usage And Synthesis |
Chemical Properties | BEIGE CRYSTALLINE NEEDLES | Production Methods | 2,4,6-Trimethylphenol is the main product (more than 80%) of the gas phase alkylation of phenol with excess methanol (molar ratio 1 : 5) at 450 ℃ on magnesium oxide catalysts, which are doped with alkali or other metal oxides (e.g., V2O5, SrO). 2,6-Xylenol and 2,3,4,6-tetramethylphenol are the main byproducts. | Synthesis Reference(s) | Journal of the American Chemical Society, 107, p. 1060, 1985 DOI: 10.1021/ja00290a053 Synthetic Communications, 18, p. 1207, 1988 DOI: 10.1080/00397918808060912 | Flammability and Explosibility | Not classified | Purification Methods | Crystallise the phenol from water and sublime it in vacuo. [Beilstein 6 IV 3253.] |
| 2,4,6-Trimethylphenol Preparation Products And Raw materials |
Raw materials | Phenol-->Methanol | Preparation Products | 3,5-Dimethyl-4-hydroxybenzaldehyde-->4,4'-METHYLENEBIS(2,6-DIMETHYLPHENOL)-->2-Methylcyclopentanone-->2,6-Dimethylphenol-->1,3,5-TRIMETHYL-2-PHENOXY-BENZENE-->Benzoic acid, 2,4,6-trimethyl-, 2,4,6-trimethylphenyl ester |
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