Chemistry:ABCN
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| Names | |
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| Systematic IUPAC name
1,1′-Diazene-1,2-diyldicyclohexanecarbonitrile | |
| Identifiers | |
3D model (JSmol)
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| Abbreviations | ACHN |
| 960744 | |
| ChemSpider | |
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PubChem CID
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| UNII | |
| UN number | 3226 |
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| Properties | |
| C14H20N4 | |
| Molar mass | 244.342 g·mol−1 |
| Melting point | 114 to 118[1] °C (237 to 244 °F; 387 to 391 K) decomposes near 80 °C |
| Hazards | |
| GHS pictograms |  
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| GHS Signal word | Danger |
| H242, H315, H319, H335 | |
| P261, P305+351+338 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
1,1′-Azobis(cyclohexanecarbonitrile) or ACHN is a radical initiator.[1] The molecular formula is NCC6H10N=NC6H10CN. It is a white solid that is soluble in aromatic solvents.[2]
ACHN has a 10-hour half-life in toluene at 88 °C.[1]
See also
- Azobisisobutylonitrile (AIBN) is another commonly used free radical initiator
References
- ↑ 1.0 1.1 1.2 1,1′-Azobis(cyclohexanecarbonitrile) at Sigma-Aldrich
- ↑ Steven A. Kates, Fernando Albericio (2001). "1,1'-Azobis-1-cyclohexanenitrile". E-EROS Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.ra120.
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