Cyclopentane
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| Names | |||
|---|---|---|---|
| Preferred IUPAC name Cyclopentane | |||
| Other names pentamethylene | |||
| Identifiers | |||
| 3D model (JSmol) | |||
| ChEBI | |||
| ChemSpider | |||
| ECHA InfoCard | 100.005.470 | ||
| EC Number | 
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| PubChem CID | |||
| RTECS number | 
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| UNII | |||
| CompTox Dashboard (EPA) | |||
| 
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| 
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| Properties | |||
| C5H10 | |||
| Molar mass | 70.1 g/mol | ||
| Appearance | clear, colorless liquid | ||
| Odor | mild, sweet | ||
| Density | 0.751 g/cm3 | ||
| Melting point | −93.9 °C (−137.0 °F; 179.2 K) | ||
| Boiling point | 49.2 °C (120.6 °F; 322.3 K) | ||
| 156 mg·l−1 (25 °C) | |||
| Solubility | soluble in ethanol, acetone, ether | ||
| Vapor pressure | 45 kPa (20 °C) | ||
| Acidity (pKa) | ~45 | ||
| −59.18·10−6 cm3/mol | |||
| Refractive index (nD) | 1.4065 | ||
| Hazards | |||
| Occupational safety and health (OHS/OSH): | |||
| Main hazards | Flammable | ||
| NFPA 704 (fire diamond) | |||
| Flash point | −37.2 °C (−35.0 °F; 236.0 K) | ||
| 361 °C (682 °F; 634 K) | |||
| Explosive limits | 1.1%–8.7% | ||
| NIOSH (US health exposure limits): | |||
| PEL (Permissible) | none | ||
| REL (Recommended) | TWA 600 ppm (1720 mg/m3) | ||
| IDLH (Immediate danger) | N.D. | ||
| Related compounds | |||
| Related compounds | cyclopropane, cyclobutane, cyclohexane | ||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |||
Cyclopentane (also called C pentane) is a highly flammable alicyclic hydrocarbon with chemical formula C5H10 and CAS number 287-92-3, consisting of a ring of five carbon atoms each bonded with two hydrogen atoms above and below the plane. It is a colorless liquid with a petrol-like odor. Its freezing point is −94 °C and its boiling point is 49 °C. Cyclopentane is in the class of cycloalkanes, being alkanes that have one or more carbon rings. It is formed by cracking cyclohexane in the presence of alumina at a high temperature and pressure.
It was first prepared in 1893 by the German chemist Johannes Wislicenus.