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Names | |||
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Preferred IUPAC name
Cyclopropane[2] | |||
Identifiers | |||
3D model (JSmol)
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ChEBI | |||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.000.771 | ||
KEGG | |||
PubChem CID
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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
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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).
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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.[3]
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.