AIBN MSDS PDF

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TCI uses cookies to personalize and improve your user experience. By continuing on our website, you accept the use of cookies. Please note that the latest information on the storage temperature for the products is described on our website. Please note that we cannot offer bulk quantities for some products. AIBN 2,2'-Azodiisobutyronitrile. Request Bulk Quote. General Information. H : Suspected of damaging fertility or the unborn child. H : May cause damage to organs through prolonged or repeated exposure.

H : Harmful to aquatic life with long lasting effects. H : Heating may cause a fire. P : Avoid release to the environment.

P : Do not eat, drink or smoke when using this product. P : Do not handle until all safety precautions have been read and understood. No smoking. P : Keep only in original container. P : Obtain special instructions before use. P : Use only outdoors or in a well-ventilated area. P : Wash skin thoroughly after handling. Rinse mouth. P : Store away from other materials.

Keep container tightly closed. Keep cool. P : Store locked up. PubMed Literature. The requested SDS is not available. Other Documents Specifications. Product Categories Chemistry Synthetic Reagents. Radical Chemistry. Radical Initiators [Synthetic Reagents]. Nitriles [Chemical Structural Class]. Dinitriles [Chemical Structural Class]. Polymerization Reagents. Polymerization Initiators. Thermal Polymerization Initiators.

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Azobisisobutyronitrile (AIBN)

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V-60 (AIBN)

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. In its most characteristic reaction, AIBN decomposes , eliminating a molecule of nitrogen gas to form two 2-cyanopropyl radicals:. These radicals can initiate free-radical polymerizations and other radical-induced reactions. For instance, a mixture of styrene and maleic anhydride in toluene will react if heated, forming the copolymer upon addition of AIBN. Another example of a radical reaction that can be initiated by AIBN is the anti-Markovnikov hydrohalogenation of alkenes. AIBN is produced from acetone cyanohydrin and hydrazine , then followed by oxidation: [1].

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