Cyclopropane
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| Names | |||
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| Preferred IUPAC name Cyclopropane | |||
| Identifiers | |||
| 3D model (JSmol) | |||
| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.000.771 | ||
| KEGG | |||
| PubChem CID | |||
| UNII | |||
| UN number | 1027 | ||
| CompTox Dashboard (EPA) | |||
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| Properties | |||
| C3H6 | |||
| Molar mass | 42.08 g/mol | ||
| Appearance | Colorless gas | ||
| Odor | Sweet, ethereal | ||
| Density | 1.879 g/L (1 atm, 0 °C) 680 g/L (liquid) | ||
| Melting point | −128 °C (−198 °F; 145 K) | ||
| Boiling point | −32.9 °C (−27.2 °F; 240.2 K) | ||
| 502 mg/L | |||
| Vapor pressure | 640 kPa (20 °C) 1350 kPa (50 °C) | ||
| Acidity (pKa) | ~46 | ||
| −39.9·10−6 cm3/mol | |||
| Hazards | |||
| Occupational safety and health (OHS/OSH): | |||
| Main hazards | Highly flammable Asphyxiant | ||
| GHS labelling: | |||
| Danger | |||
| NFPA 704 (fire diamond) | |||
| 495 °C (923 °F; 768 K) | |||
| Explosive limits | 2.4 % (lower) 10.4 % (upper) | ||
| Safety data sheet (SDS) | Air Liquide | ||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |||
Cyclopropane is the cycloalkane with the molecular formula (CH2)3, consisting of three methylene groups (CH2) linked to each other to form a triangular ring. The small size of the ring creates substantial ring strain in the structure. Cyclopropane itself is mainly of theoretical interest but many of its derivatives - cyclopropanes - are of commercial or biological significance.
Cyclopropane was used as a clinical inhalational anesthetic from the 1930s through the 1980s. The substance's high flammability poses a risk of fire and explosions in operating rooms due to its tendency to accumulate in confined spaces, as its density is higher than that of air.