Names | |
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Preferred IUPAC name
(2R)-2-Methyloxirane (2S)-2-Methyloxirane | |
Other names
Propylene oxide
Epoxypropane Propylene epoxide 1,2-Propylene oxide Methyl oxirane 1,2-Epoxypropane Propene oxide Methyl ethylene oxide Methylethylene oxide | |
Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.000.800 |
EC Number |
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KEGG | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C3H6O | |
Molar mass | 58.080 g·mol−1 |
Appearance | Colourless liquid |
Odor | benzene-like[1] |
Density | 0.859 g/cm3[2] |
Melting point | −111.9 °C (−169.4 °F; 161.2 K)[2] |
Boiling point | 35 °C (95 °F; 308 K)[2] |
41% (20 °C)[1] | |
Vapor pressure | 445 mmHg (20 °C)[1] |
−4.25×10−5 cm3/mol[3] | |
Refractive index (nD)
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1.3660[2] |
Thermochemistry | |
Heat capacity (C)
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120.4 J·(K·mol)−1 |
Std molar
entropy (S⦵298) |
196.5 J·(K·mol)−1 |
Std enthalpy of
formation (ΔfH⦵298) |
−123.0 kJ·mol−1[4] |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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Extremely flammable[5][6] |
GHS labelling: | |
Danger | |
NFPA 704 (fire diamond) | |
Flash point | −37 °C (−35 °F; 236 K) |
747 °C (1,377 °F; 1,020 K) | |
Explosive limits | 2.3–36%[1] |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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660 mg/kg (guinea pig, oral) 380 mg/kg (rat, oral) 440 mg/kg (mouse, oral) 1140 mg/kg (rat, oral) 690 mg/kg (guinea pig, oral)[7] |
LC50 (median concentration)
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1740 ppm (mouse, 4 h) 4000 ppm (rat, 4 h)[7] |
LCLo (lowest published)
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2005 ppm (dog, 4 h) 4000 ppm (guinea pig, 4 h)[7] |
NIOSH (US health exposure limits): | |
PEL (Permissible)
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TWA 100 ppm (240 mg/m3)[1] |
REL (Recommended)
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Ca[1] |
IDLH (Immediate danger)
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Ca [400 ppm][1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Propylene oxide is an acutely toxic and carcinogenic organic compound with the molecular formula C3H6O. This colourless volatile liquid with an odour similar to ether, is produced on a large scale industrially. Its major application is its use for the production of polyether polyols for use in making polyurethane plastics. It is a chiral epoxide, although it is commonly used as a racemic mixture.
This compound is sometimes called 1,2-propylene oxide to distinguish it from its isomer 1,3-propylene oxide, better known as oxetane.