Cyclopropane
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.
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Names | |||
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Preferred IUPAC name
Cyclopropane | |||
Identifiers | |||
3D model (JSmol) |
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ChEBI | |||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.000.771 | ||
KEGG | |||
PubChem CID |
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UNII | |||
CompTox Dashboard (EPA) |
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Properties | |||
C3H6 | |||
Molar mass | 42.08 g/mol | ||
Appearance | Colorless gas | ||
Odor | Sweet | ||
Density | 1.879 g/L (1 atm, 0 °C) | ||
Melting point | −128 °C (−198 °F; 145 K) | ||
Boiling point | −33 °C (−27 °F; 240 K) | ||
Acidity (pKa) | ~46 | ||
-39.9·10−6 cm3/mol | |||
Hazards | |||
Occupational safety and health (OHS/OSH): | |||
Main hazards |
Highly flammable Asphyxiant | ||
NFPA 704 (fire diamond) | |||
Safety data sheet (SDS) | External MSDS | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references |
Cyclopropane was used as a clinical inhalational anesthetic from the 1930s through the 1980s. Its high flammability posed a risk of fire and even explosions in the operating room.
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