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Isobutane

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Isobutane
Names
IUPAC names
Methylpropane
2-Methylpropane
Other names
Isobutane
Identifiers
3D model (JSmol)
ECHA InfoCard 100.000.780 Edit this at Wikidata
E number E943b (glazing agents, ...)
  • CC(C)C
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)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g. propaneInstability (yellow): no hazard codeSpecial hazards (white): no code
1
4
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).

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

Structures of the two isomers of butane

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

References

  1. ^ Patent Watch, July 31, 2006.
  2. ^ Panico, R.; & Powell, W. H. (Eds.) (1994). A Guide to IUPAC Nomenclature of Organic Compounds 1993. Oxford: Blackwell Science. ISBN 0-632-03488-2.{{cite book}}: CS1 maint: multiple names: authors list (link) http://www.acdlabs.com/iupac/nomenclature/93/r93_679.htm

External links