Hexane
Hexane is an organic compound with the chemical formula C6H14. It is an alkane with 6 carbon atoms. "Hexane" can mean any of the 5 structural isomers (meaning compounds with the same chemical formula but a different shape) it has. IUPAC naming says that "hexane" only means the isomer with no branches, with the other 4 having different names.
| Hexane | |
|---|---|
| |
| |
| |
| |
| IUPAC name | Hexane[1] |
| Other names | Sextane[2] |
| Identifiers | |
| CAS number | |
| PubChem | |
| EC number | 203-777-6 |
| DrugBank | DB02764 |
| KEGG | C11271 |
| MeSH | |
| ChEBI | CHEBI:29021 |
| RTECS number | MN9275000 |
| SMILES | CCCCCC |
| Beilstein Reference | 1730733 |
| Gmelin Reference | 1985 |
| Properties | |
| Molecular formula | C6H14 |
| Molar mass | 86.18 g mol-1 |
| Appearance | Colorless liquid |
| Odor | Petrolic |
| Density | 0.6606 g mL−1[3] |
| Melting point |
Expression error: Unrecognized word "to". °C, 177 to 179 K, Expression error: Unrecognized word "to". °F |
| Boiling point | |
| Solubility in water | 9.5 mg L−1 |
| log P | 3.764 |
| Vapor pressure | 17.60 kPa (at 20.0 °C) |
| kH | 7.6 nmol Pa−1 kg−1 |
| λmax | 200 nm |
| −74.6·10−6 cm3/mol | |
| Refractive index (nD) | 1.375 |
| Viscosity | 0.3 mPa·s |
| Thermochemistry | |
| Std enthalpy of formation ΔfH |
−199.4–−198.0 kJ mol−1 |
| Std enthalpy of combustion ΔcH |
−4180–−4140 kJ mol−1 |
| Standard molar entropy S |
296.06 J K−1 mol−1 |
| Specific heat capacity, C | 265.2 J K−1 mol−1 |
| Hazards | |
| Main hazards | Reproductive toxicity – After aspiration, pulmonary oedema, pneumonitis, and death [4] |
| NFPA 704 |
3
1
0
|
| Explosive limits | 1.2–7.7% |
| U.S. Permissible exposure limit (PEL) |
TWA 500 ppm (1800 mg/m3)[5] |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
Hexane is often part of modern gasoline. Pure hexane has no color and is quite unreactive.
Hexane Media
hexane isomer
hexane isomer
hexane isomer
hexane isomer
References
- ↑ "n-hexane – Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 16 September 2004. Identification and Related Records. Archived from the original on 8 March 2012. Retrieved 31 December 2011.
- ↑ Hofmann, August Wilhelm Von (1 January 1867). "I. On the action of trichloride of phosphorus on the salts of the aromatic monamines". Proceedings of the Royal Society of London. 15: 54–62. doi:10.1098/rspl.1866.0018. S2CID 98496840. Archived from the original on 28 April 2018. Retrieved 28 April 2018 – via rspl.royalsocietypublishing.org.
- ↑ William M. Haynes (2016). CRC Handbook of Chemistry and Physics (97th ed.). Boca Raton: CRC Press. p. 3–298. ISBN 978-1-4987-5429-3.
- ↑ GHS Classification on [PubChem]
- ↑ NIOSH Pocket Guide to Chemical Hazards. "#0322". National Institute for Occupational Safety and Health (NIOSH).