| Identification | Back Directory | [Name]
6-AMINO CAPRONITRILE | [CAS]
2432-74-8 | [Synonyms]
TIMTEC-BB SBB008486
w-Aminocapronitrile
ε-Aminocapronitrile
6-amino-hexanenitril
6-aminohexanonitrile
6-AMINO CAPRONITRILE
6-AMINOHEXANENITRILE
6-azanylhexanenitrile
Hexanenitrile, 6-amino-
OMEGA-AMINOCAPRONITRILE
6-Aminohexanenitrile hcl
.epsilon.-Aminocaprylonitrile | [EINECS(EC#)]
219-409-2 | [Molecular Formula]
C6H12N2 | [MDL Number]
MFCD00009822 | [MOL File]
2432-74-8.mol | [Molecular Weight]
112.17 |
| Chemical Properties | Back Directory | [Melting point ]
-31.3°C | [Boiling point ]
200.13°C (rough estimate) | [density ]
0.8929 (rough estimate) | [refractive index ]
1.4475 | [storage temp. ]
Refrigerator, Under inert atmosphere | [solubility ]
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | [form ]
Oil | [pka]
10.38±0.10(Predicted) | [color ]
Colourless to Pale Yellow | [InChI]
InChI=1S/C6H12N2/c7-5-3-1-2-4-6-8/h1-5,7H2 | [InChIKey]
KBMSFJFLSXLIDJ-UHFFFAOYSA-N | [SMILES]
C(#N)CCCCCN | [EPA Substance Registry System]
Hexanenitrile, 6-amino- (2432-74-8) |
| Hazard Information | Back Directory | [Uses]
6-Aminohexanenitrile is a compound useful in organic synthesis and other chemical processes. | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 46, p. 1263, 1981 DOI: 10.1021/jo00320a008 | [Purification Methods]
When 6-amino capronitrile is produced by partial hydrogenation of
adiponitrile, hexamethylenediamine and tetrahydroazepine (THA) are also coproduced. The hexamethylenediamine can be easily removed from the mixture by simple distillation. The process for the recovery of 6-amino capronitrile from a mixture containing 6-amino capronitrile and THA which comprises (a) heating said mixture at a temperature about 235
℃, to convert THA to higher boiling compounds; (b) then distilling the 6-amino capronitrile from the resulting mixture. |
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