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2,6-Di-tert-butylphenol 128-39-2CAS NO.: 128-39-2 CAS NO.128-39-2
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- Min.Order: 1 Kilogram
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- Available Specifications:
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- Product Details
Keywords
- 2,6-Di-tert-butylphenol
- 2,6-DI-T-BUTYLPHENOL
- 99.5% 2,6-Di-tert-butylphenol
Quick Details
- ProName: 2,6-Di-tert-butylphenol 128-39-2CAS NO...
- CasNo: 128-39-2
- Molecular Formula: C14H22O
- Appearance: White solid
- Application: Adhesive and Sealant
- DeliveryTime: in stock
- PackAge: Aluminium foil bag
- Port: China main port
- ProductionCapacity: 10000 Gram/Day
- Purity: 99%
- Storage: Room temperature
- Transportation: By Sea/Air/DHL
- LimitNum: 1 Kilogram
- first class: 1-10
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4.Customs Synthesis
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Details
| Chemical Properties | white solid |
| Uses | Antioxidant for Gasoline, Jet Fuels, and Electrical Insulating Oils |
| Uses | Antioxidant Intermediate, Pharmaceuticals |
| General Description | Odorless colorless to light yellow solid or liquid. Floats on water. Freezing point is 97°F. |
| Air & Water Reactions | Insoluble in water. |
| Reactivity Profile | Phenols, such as 2,6-Di-tert-butylphenol, 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 | Irritates eyes and (on prolonged contact) skin. Ingestion causes irritation of mouth and stomach. |
| Purification Methods | Crystallise the phenol from aqueous EtOH or n-hexane. [Beilstein 6 III 2061.] |