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Organic compound From Wikipedia, the free encyclopedia
m-Cymene is an organic compound classified as an aromatic hydrocarbon. Its structure consists of a benzene ring meta-substituted with a methyl group and an isopropyl group. It is a flammable colorless liquid which is nearly insoluble in water but soluble in organic solvents.
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Preferred IUPAC name
1-Methyl-3-(propan-2-yl)benzene | |
Other names
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Identifiers | |
3D model (JSmol) |
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ChEBI | |
ChemSpider | |
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Properties | |
C10H14 | |
Molar mass | 134.22 |
Appearance | colorless liquid |
Density | 0.86 g/cm3 |
Melting point | −63.8 °C (−82.8 °F; 209.3 K) |
Boiling point | 175 °C (347 °F; 448 K) |
42.5 mg/L | |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards |
Flammable |
GHS labelling: | |
Warning | |
H226 | |
P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, P501 | |
Flash point | 47.8 °C (118.0 °F; 320.9 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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In addition to m-cymene, there are two other geometric isomers called o-cymene, in which the alkyl groups are ortho-substituted, and p-cymene, in which they are para-substituted. p-Cymene is the most common and only natural isomer. The three isomers form the group of cymenes.
Cymenes can be produced by alkylation of toluene with propylene.[1][2]
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