Azepane

Azepane is the organic compound with the formula (CH₂)₆NH. It is a colorless liquid. A cyclic secondary amine, it is a precursor to several drugs and pesticides. It is produced by partial hydrogenolysis of hexamethylene diamine.[2]

Azepane

Skeletal formula of azepane Ball-and-stick model of the azepane molecule
Names
IUPAC name Azepane
Other names Hexahydroazepine Hexamethyleneimine Homopiperidine Perhydroazepine HMI azacycloheptane
Identifiers
CAS Number	111-49-9
3D model (JSmol)	Interactive image
ChEBI	CHEBI:32616
ChEMBL	ChEMBL1375444
ChemSpider	7828
ECHA InfoCard	100.003.524
PubChem CID	8119
UNII	CZD076G73R
CompTox Dashboard (EPA)	DTXSID1026879
InChI InChI=1S/C6H13N/c1-2-4-6-7-5-3-1/h7H,1-6H2 Key: ZSIQJIWKELUFRJ-UHFFFAOYSA-N InChI=1/C6H13N/c1-2-4-6-7-5-3-1/h7H,1-6H2 Key: ZSIQJIWKELUFRJ-UHFFFAOYAF
SMILES C1CCCNCC1
Properties
Chemical formula	C6H13N
Molar mass	99.177 g·mol^−1
Appearance	colorless liquid
Density	0.88 g/cm^3[1]
Melting point	−37 °C (−35 °F; 236 K)
Boiling point	138 °C (280 °F; 411 K)[1] (749 mmHg)
Hazards
Flash point	30 °C (86 °F; 303 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
verify (what is  ?)
Infobox references

Like many amines, it reacts with carbon dioxide.[3]

See also

• Azepine

References

1. "Hexamethyleneimine".
2. Karsten Eller, Erhard Henkes, Roland Rossbacher, Hartmut Höke (2005). "Amines, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a02_001.CS1 maint: uses authors parameter (link)
3. Sanz-Pérez, E. S.; Arencibia, A.; Sanz, R.; Calleja, G. (2016). "New developments on carbon dioxide capture using amine-impregnated silicas". Adsorption. 22 (4): 366–375. doi:10.1007/s10450-015-9740-2.