CasNo.80-46-6,Phenol,4-(1,1-dimethylpropyl)-,(80-46-6) Suppliers

1 Kilogram	Negotiable

Phenol,4-(1,1-dimethylpropyl)- price Phenol,4-(1,1-dimethylpropyl)- CAS 80-46-6 Phenol,4-(1,1-dimethylpropyl)- supplier in China

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4-tert-Amylphenol Chemical Properties

mp	88-89 °C(lit.)
bp	255 °C(lit.)
density	0,96 g/cm³
Fp	111 °C
Water Solubility	37 mg/L (20 ºC)
Merck	14,7142
Stability:	Stable. Incompatible with acid chlorides, acid anhydrides, strong oxidizing agents.
CAS DataBase Reference	80-46-6(CAS DataBase Reference)
NIST Chemistry Reference	Phenol, 4-(1,1-dimethylpropyl)-(80-46-6)
EPA Substance Registry System	Phenol, 4-(1,1-dimethylpropyl)-(80-46-6)

Safety Information

MSDS Information

4-tert-Amylphenol Usage And Synthesis

Chemical Properties	solid
General Description	Colorless needles or beige solid.
Air & Water Reactions	Insoluble in water.
Reactivity Profile	Phenols, such as 4-tert-Amylphenol, 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. Nitrated phenols often explode when heated. Many of them form metal salts that tend toward detonation by rather mild shock. 4-tert-Amylphenol can react with oxidizing materials.
Health Hazard	ACUTE/CHRONIC HAZARDS: 4-tert-Amylphenol is toxic by ingestion and can be absorbed through the skin. Hazardous fumes are evolved when 4-tert-Amylphenol is heated to decomposition.
Fire Hazard	4-tert-Amylphenol is combustible.