Ethylcyclohexane
|
| Identifiers
|
|
|
|
|
|
|
| ChEBI
|
|
| ChEMBL
|
|
| ChemSpider
|
|
| ECHA InfoCard
|
100.015.305 
|
| EC Number
|
|
|
|
|
| UNII
|
|
| UN number
|
1993
|
|
|
|
InChI=1S/C8H16/c1-2-8-6-4-3-5-7-8/h8H,2-7H2,1H3 Key: IIEWJVIFRVWJOD-UHFFFAOYSA-N
|
|
|
| Properties
|
|
|
C8H16
|
| Molar mass
|
112.216 g·mol−1
|
| Appearance
|
colorless liquid
|
| Density
|
0.788 g/cm3
|
| Melting point
|
−111.3 °C (−168.3 °F; 161.8 K)
|
| Boiling point
|
130–132 °C (266–270 °F; 403–405 K)
|
| Hazards
|
| GHS labelling:[1]
|
|
|
  
|
|
|
Danger
|
|
|
H225, H304, H336
|
|
|
P210, P233, P240, P241, P242, P243, P261, P271, P280, P301+P316, P303+P361+P353, P304+P340, P319, P331, P370+P378, P403+P233, P403+P235, P405, P501
|
| Flash point
|
35 °C; 95 °F; 308 K
|
|
|
238 °C; 460 °F; 511 K
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Chemical compound
Ethylcyclohexane is an organic compound with the formula C6H11C2H5. The molecule consists of an ethyl group attached to a cyclohexane ring. It is a typical naphthene in petroleum. It can be produced by hydrogenation of ethylbenzene and by hydrodeoxygenation of lignin.[2]
References
- ^ "Ethylcyclohexane". pubchem.ncbi.nlm.nih.gov.
- ^ Zhao, Chen; He, Jiayue; Lemonidou, Angeliki A.; Li, Xuebing; Lercher, Johannes A. (2011). "Aqueous-phase hydrodeoxygenation of bio-derived phenols to cycloalkanes". Journal of Catalysis. 280: 8–16. doi:10.1016/j.jcat.2011.02.001.
