- 6-tert-Butyl-3-methylphenol
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- $6.00 / 1KG
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2024-01-18
- CAS:88-60-8
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
- 6-tert-Butyl-m-cresol
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- $0.00 / 190kg
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2023-11-01
- CAS:88-60-8
- Min. Order: 1000kg
- Purity: 99.9%
- Supply Ability: 5000 tons
- 6-tert-Butyl-m-cresol
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- $0.00 / 25KG
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2023-10-24
- CAS:88-60-8
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 50000KG/month
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| | 6-tert-Butyl-m-cresol Basic information |
| | 6-tert-Butyl-m-cresol Chemical Properties |
| Melting point | 20 °C | | Boiling point | 117-118 °C12 mm Hg(lit.) | | density | 0.964 g/mL at 25 °C(lit.) | | vapor pressure | 3Pa at 23℃ | | refractive index | n20/D 1.519(lit.) | | Fp | 222 °F | | storage temp. | Inert atmosphere,Room Temperature | | Water Solubility | Insoluble in water | | pka | 11.45±0.10(Predicted) | | Specific Gravity | 0.9590.964 | | color | Colorless to Red to Green | | Odor | at 0.10 % in dipropylene glycol. russian leather | | Odor Type | animal | | LogP | 3.97 | | CAS DataBase Reference | 88-60-8(CAS DataBase Reference) | | NIST Chemistry Reference | Phenol, 2-(1,1-dimethylethyl)-5-methyl-(88-60-8) | | EPA Substance Registry System | 6-tert-Butyl-m-cresol (88-60-8) |
| | 6-tert-Butyl-m-cresol Usage And Synthesis |
| Chemical Properties | clear colorless viscous liquid | | Synthesis Reference(s) | Tetrahedron Letters, 31, p. 6977, 1990 DOI: 10.1016/S0040-4039(00)97220-4 | | General Description | A clear colorless liquid. Flash point 116°F. Melting point 74°F. Less dense than water and insoluble in water. Used as a disinfectant, to make rubber, as a lubricating oil additive, and for many other uses. | | Air & Water Reactions | Flammable. Insoluble in water. | | Reactivity Profile | Phenols, such as 6-tert-Butyl-m-cresol, do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases. Such heating may initiate polymerization of the organic compound. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). The reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid. | | Health Hazard | Inhalation or contact with material may irritate or burn skin and eyes. Fire may produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution. |
| | 6-tert-Butyl-m-cresol Preparation Products And Raw materials |
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