| | 2-tert-Butylphenol Basic information |
| | 2-tert-Butylphenol Chemical Properties |
| Melting point | −7 °C(lit.) | | Boiling point | 224 °C(lit.) | | density | 0.978 g/mL at 25 °C(lit.) | | vapor pressure | 0.05 mm Hg ( 20 °C) | | refractive index | n20/D 1.523(lit.) | | Fp | >230 °F | | storage temp. | Store below +30°C. | | solubility | 0.97g/l soluble | | pka | 10.62(at 25℃) | | form | clear liquid | | color | Colorless to Light yellow to Light orange | | Water Solubility | 0.23 g/100 mL (20 ºC) | | BRN | 1907120 | | Stability: | Light Sensitive | | LogP | 3.3 at 23℃ | | CAS DataBase Reference | 88-18-6(CAS DataBase Reference) | | NIST Chemistry Reference | Phenol, 2-(1,1-dimethylethyl)-(88-18-6) | | EPA Substance Registry System | 2-tert-Butylphenol (88-18-6) |
| | 2-tert-Butylphenol Usage And Synthesis |
| Chemical Properties | CLEAR LIQUID | | Chemical Properties | The butylphenols include several isomers.
Solid butylphenols (28805-86-9) generally have properties
similar to the above: | | Uses | Flavors, Fragrances, Insecticides, Phenolic Resins, Antioxidant Intermediate | | Uses | 2-tert-Butylphenol is used pharmaceutical intermediates. | | Definition | ChEBI: 2-tert-Butylphenol is an alkylbenzene. | | Potential Exposure | Butylphenols may be used as intermediates in manufacturing varnish and lacquer resins; as a
germicidal agent in detergent disinfectants; as a pour point
depressant, in motor-oil additives; de-emulsifier for oil;
soap-antioxidant, plasticizer, fumigant, and insecticide | | Shipping | UN2430 Alkylphenols, solid, n.o.s. (including
C2-C12 homologues), Hazard class: 8; Labels: 8—
Corrosive material | | Incompatibilities | Vapors may form explosive mixture with
air. These phenol/cresol materials can react with oxidizers;
reaction may be violent. 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 cause the gas to ignite and explode.
Heat is also generated by the acid-base reaction with bases;
such heating may initiate polymerization of the organic
compound. React with boranes, alkalies, aliphatic amines,
amides, nitric acid, sulfuric acid. Phenols are sulfonated
very readily (for example, by concentrated sulfuric acid at
room temperature). These reactions generate heat. Phenols
are also nitrated very rapidly, even by dilute nitric acid and
can explode when heated. Many phenols form metal salts
that may be detonated by mild shock |
| | 2-tert-Butylphenol Preparation Products And Raw materials |
|
