Revision as of 19:50, 30 May 2011 editSpinach Dip (talk | contribs)Pending changes reviewers, Rollbackers1,706 edits seperate sections← Previous edit | Revision as of 08:22, 22 August 2011 edit undoNao1958 (talk | contribs)Extended confirmed users546 editsNo edit summaryNext edit → | ||
Line 2: | Line 2: | ||
| Watchedfields = changed | | Watchedfields = changed | ||
| verifiedrevid = 396294932 | | verifiedrevid = 396294932 | ||
| Name = |
| Name = | ||
| ImageFile_Ref = {{chemboximage|correct|??}} | | ImageFile_Ref = {{chemboximage|correct|??}} | ||
| ImageFile = AIBN Structural Formulae.png | | ImageFile = AIBN Structural Formulae.png | ||
Line 29: | Line 29: | ||
| MolarMass = 164.21 g/mol | | MolarMass = 164.21 g/mol | ||
| Appearance = white crystalline | | Appearance = white crystalline | ||
| Density = 1.1 | | Density = 1.1 g cm<sup>−3</sup> | ||
| Solubility = |
| Solubility = | ||
| |
| MeltingPtCL = 103 | ||
| |
| MeltingPtCH = 105 | ||
| BoilingPt = | |||
}} | }} | ||
| Section3 = {{Chembox Structure | | Section3 = {{Chembox Structure | ||
| Dipole = |
| Dipole = | ||
}} | }} | ||
| Section7 = {{Chembox Hazards | | Section7 = {{Chembox Hazards | ||
Line 41: | Line 42: | ||
| ExternalMSDS = | | ExternalMSDS = | ||
| EUClass = | | EUClass = | ||
| FlashPt = |
| FlashPt = | ||
}} | }} | ||
}} | }} |
Revision as of 08:22, 22 August 2011
Names | |
---|---|
IUPAC name 2,2′-Azobis(2-methylpropionitrile) | |
Other names
Azobisisobutyronitrile Azobisisobutylonitrile AIBN | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.001.030 |
PubChem CID | |
CompTox Dashboard (EPA) | |
InChI
| |
SMILES
| |
Properties | |
Chemical formula | C8H12N4 |
Molar mass | 164.21 g/mol |
Appearance | white crystalline |
Density | 1.1 g cm |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
Azobisisobutyronitrile is a compound often used as a foamer in plastics and rubber and as a radical initiator. It is commonly known as AIBN. Its most common chemical reaction is one of decomposition, eliminating a molecule of nitrogen gas to form two 2-cyanoprop-2-yl radicals:
These radicals can be used to initiate free radical polymerizations and other radical reactions. For instance a mixture of styrene and maleic anhydride in toluene will react if heated, forming the polystyrene polymer, only very slowly unless an initiator such an AIBN is present. Another example of a radical reaction that can be initiated by AIBN is the anti-Markovnikov hydrohalogenation of alkenes.
Safety
AIBN is safer to use than benzoyl peroxide (another radical initiator) because the risk of explosion is far smaller. However, it is considered a flammable solid. It is soluble in methanol and ethanol, but is insoluble in water. It can explode if dissolved in acetone. AIBN is highly toxic. A respirator/dust mask, protective gloves, & safety glasses should be worn when handling AIBN.
Several water-soluble azo initiators similar to AIBN are manufactured by DuPont and Wako.
See also
- 1,1'-Azobis(cyclohexanecarbonitrile) or ABCN is another free radical initiator
References
External links
- SIDS Initial Assessment Report for 2,2’-Azobis(2-methylpropionitrile) from the Organisation for Economic Co-operation and Development (OECD)