2-Methyl-1-pentene

Chemical properties

CLEAR COLOURLESS LIQUID

Physical properties

Clear, colorless flammable liquid with an unpleasant hydrocarbon odor.

The Uses of 2-Methyl-1-pentene

Organic synthesis, flavors, perfumes,medicines, dyes, oils, resins.

The Uses of 2-Methyl-1-pentene

2-Methyl-1-pentene is prepared from 2-Methyl-1-pentene. 2-methyl-1-pentene is used in copolymerization of ethylene catalyzed by nonbridged half-titanocenes. The isomerization of 2-methyl-1-pentene leads to anionic activation of c-h bonds in olefins.

Definition

ChEBI: 2-methyl-1-pentene is an alkene that is pent-1-ene carrying a methyl group at position 2. It has a role as a human metabolite. It is an alkene and a volatile organic compound. It derives from a hydride of a pentane.

General Description

Colorless liquid. Flash point -15°F. Floats on water. Irritating vapor.

Air & Water Reactions

Highly flammable. Insoluble in water.

Reactivity Profile

2-Methyl-1-pentene may react vigorously with strong oxidizing agents. May react exothermically with reducing agents to release hydrogen gas. In the presence of various catalysts (such as acids) or initiators, may undergo exothermic addition polymerization reactions.

Hazard

Flammable, dangerous fire risk.

Health Hazard

INHALATION: May produce anesthetic effects. EYES: Moderate eye irritation possible.

Fire Hazard

Behavior in Fire: Can react vigorously with oxidizing materials.

Source

California Phase II reformulated gasoline contained 2-methyl-1-pentene at a concentration of 1.25 g/kg. Gas-phase tailpipe emission rates from gasoline-powered automobiles with and without catalytic converters were 0.23 and 26.6 mg/km, respectively (Schauer et al., 2002).

Environmental Fate

Photolytic. The reported reaction rate constants for the reaction of 2-methyl-1-pentene with OH radicals and ozone in the atmosphere are 1.05 x 10^-17 and 6.26 x 10^-11 cm³/molecule?sec, respectively (Atkinson and Carter, 1984; Atkinson, 1985).
Chemical/Physical. Complete combustion in air yields carbon dioxide and water.

Purification Methods

Water is removed, and formation of peroxides is prevented by several vacuum distillations of 2-methyl-1-pentene from sodium. It is stored with sodium-potassium alloy. [Beilstein 1 IV 841.]