Azobisisobutyronitrile

Azobisisobutyronitrile
Names
IUPAC name
2,2′-Azobis(2-methylpropionitrile), 2-(azo(1-cyano-1-methylethyl))-2-methylpropane nitrile
Other names
Azobisisobutyronitrile
Azobisisobutylonitrile
AIBN
Identifiers
78-67-1 YesY
Abbreviations AIBN
ChemSpider 6299 YesY
EC Number 201-132-3
Jmol interactive 3D Image
PubChem 6547
Properties
C8H12N4
Molar mass 164.21 g/mol
Appearance white crystals
Density 1.1 g cm−3
Melting point 103 to 105 °C (217 to 221 °F; 376 to 378 K)
Hazards
R-phrases R11, R25, R37/38, R41
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Azobisisobutyronitrile (abbreviated AIBN) is an organic compound with the formula [(CH3)2C(CN)]2N2. 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.

Mechanism

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

Production and analogues

AIBN is produced from acetone cyanohydrin and hydrazine, then followed by oxidation:[1]

2 (CH3)2C(CN)OH + N2H4 → [(CH3)2C(CN)]2N2H2 + 2 H2O
[(CH3)2C(CN)]2N2H2 + Cl2 → [(CH3)2C(CN)]2N2 + 2 HCl

Related diazo compounds behave similarly, e.g. 1,1'-azobis(cyclohexanecarbonitrile). Water-soluble azo initiators are also available.[2][3]

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 °C. A respirator dust mask, protective gloves and safety glasses are recommended.

References

  1. Jean-Pierre Schirmann, Paul Bourdauducq "Hydrazine" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2002. doi:10.1002/14356007.a13_177.
  2. Product Grades
  3. Water soluble Azo initiators

External links

This article is issued from Wikipedia - version of the Monday, November 16, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.