Isobutane
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Names | |||
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IUPAC names
Methylpropane
2-Methylpropane | |||
Other names
Isobutane
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Identifiers | |||
3D model (JSmol)
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ECHA InfoCard | 100.000.780 | ||
E number | E943b (glazing agents, ...) | ||
CompTox Dashboard (EPA)
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Properties | |||
C4H10 | |||
Molar mass | 58.124 g·mol−1 | ||
Appearance | colorless gas | ||
Density | 2.51 kg/m3, gas (15 °C, 1 atm) 593.4 kg/m3, liquid | ||
Melting point | −159.6 °C (−255.3 °F; 113.5 K) | ||
Boiling point | −11.7 °C (10.9 °F; 261.4 K) | ||
Insoluble | |||
Hazards | |||
NFPA 704 (fire diamond) | |||
Flash point | flammable gas | ||
Explosive limits | 1.8–8.4% | ||
Related compounds | |||
Supplementary data page | |||
Isobutane (data page) | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Isobutane, also known as methylpropane or 2-methylpropane, is an alkane, isomeric with butane. Recent concerns with depletion of the ozone layer by freon gases have led to increased use of isobutane as a gas for refrigeration systems, especially in domestic refrigerators and freezers, and as a propellant in aerosol sprays. When used as a refrigerant or a propellant, isobutane is also known as R-600a. Some portable camp stoves use a mixture of isobutane with propane, usually 80:20. Isobutane is used as a feedstock in the petrochemical industry, for example in the synthesis of isooctane.[1]
Its UN number (for hazardous substances see shipping) is UN 1969.
Isobutane is the R group for the amino acid leucine.
Nomenclature
![](http://upload.wikimedia.org/wikipedia/commons/4/4b/N%26i-butane.png)
Isobutane is the trivial name retained by the International Union of Pure and Applied Chemistry (IUPAC) in its 1993 Recommendations for the Nomenclature of Organic Chemistry.[2]
Methylpropane is the systematic name. The substituent number (2-) is unnecessary because there is no isomer of this molecule with methylpropane as part of its name.
Uses
- As a refrigerant.
- As a propellant for aerosol cans and foam products, such as reddi wip.
References
- ^ Patent Watch, July 31, 2006.
- ^ Panico, R.; & Powell, W. H. (Eds.) (1994). A Guide to IUPAC Nomenclature of Organic Compounds 1993. Oxford: Blackwell Science. ISBN 0-632-03488-2.
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: CS1 maint: multiple names: authors list (link) http://www.acdlabs.com/iupac/nomenclature/93/r93_679.htm
External links
- International Chemical Safety Card 0901
- NIOSH Pocket Guide to Chemical Hazards
- IUPAC Nomenclature of Organic Chemistry (online version of the "Blue Book")
- Data from Air Liquide