Azobisisobutyronitrile (abbreviated AIBN) is an organic compound with the formula . This white powder is soluble in alcohols and common organic solvents but is insoluble in water. It is often used as a foamer in plastics and rubber and as a radical initiator.

As an azo initiator, radicals resulting from AIBN have multiple benefits over common organic peroxides. For example, they do not have oxygenated byproducts or much yellow discoloration. Additionally, they do not cause too much grafting and therefore are often used when making adhesives, acrylic fibers, detergents, etc.

Mechanism of decomposition

In its most characteristic reaction, AIBN decomposes, eliminating a molecule of nitrogen gas to form two 2-cyanoprop-2-yl radicals:

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Because azobisisobutyronitrile readily gives off free radicals, it is often used as a radical initiator. This happens at temperatures above 40&nbsp;°C, but in experiments is more commonly done at temperatures between 66&nbsp;°C and 72&nbsp;°C. This decomposition has a ΔG<sup>‡</sup> of 131&nbsp;kJ/mol The resulting tributyltin radical can be used for removal of a bromine atom.

AIBN-derived radicals abstract a hydrogen from HBr to give a bromine radical, which can add to alkenes. This type of hydrohalogenation of an alkene proceeds with anti-Markovnikov selectivity.

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Production and analogues

AIBN is produced in two steps from acetone cyanohydrin. Reaction with hydrazine gives the substituted dialkylhydrazine. In the second step, the hydrazine is oxidized to the azo derivative:

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Related azo compounds behave similarly, such as 1,1′-azobis(cyclohexanecarbonitrile). Water-soluble azo initiators are also available.

Safety

AIBN is safer to use than benzoyl peroxide (another radical initiator) because the risk of explosion is far less. However, it is still considered as an explosive compound, decomposing above 65&nbsp;°C. A respirator dust mask, protective gloves and safety glasses are recommended. Pyrolysis of AIBN without a trap for the formed 2-cyanopropyl radicals results in the formation of tetramethylsuccinonitrile, which is highly toxic.

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