| |
| |
| |
| Names | |
|---|---|
|
Systematic IUPAC name
1,1′-Diazene-1,2-diyldicyclohexanecarbonitrile | |
| Identifiers | |
3D model (
JSmol)
|
|
| Abbreviations | ACHN |
| 960744 | |
| ChemSpider | |
| ECHA InfoCard | 100.016.595 |
| EC Number |
|
PubChem
CID
|
|
| UNII | |
| UN number | 3226 |
CompTox Dashboard (
EPA)
|
|
| |
| |
| 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 labelling: | |
| |
| Danger | |
| H242, H315, H319, H335 | |
| P261, P305+P351+P338 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
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]
- Azobisisobutylonitrile (AIBN) is another commonly used free radical initiator
- ^ a b c 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.
 | This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
|
| |
|
| |
|
| |
| Names | |
|---|---|
|
Systematic IUPAC name
1,1′-Diazene-1,2-diyldicyclohexanecarbonitrile | |
| Identifiers | |
3D model (
JSmol)
|
|
| Abbreviations | ACHN |
| 960744 | |
| ChemSpider | |
| ECHA InfoCard | 100.016.595 |
| EC Number |
|
PubChem
CID
|
|
| UNII | |
| UN number | 3226 |
CompTox Dashboard (
EPA)
|
|
| |
| |
| 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 labelling: | |
|
| |
| Danger | |
| H242, H315, H319, H335 | |
| P261, P305+P351+P338 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
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]
- Azobisisobutylonitrile (AIBN) is another commonly used free radical initiator
- ^ a b c 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.
|
| This article about an organic compound is a stub. You can help Wikipedia by expanding it. |