Template:Chembox PINTemplate:Chembox SystematicNameTemplate:Chembox OtherNamesTemplate:Chembox ExternalMSDSTemplate:Chembox HPhrases
Skeletal formula of isobutane Skeletal formula of isobutane with all explicit hydrogens added
Ball and stick model of isobutane Spacefill model of isobutane
CAS number 75-28-5 File:Yes check.svgY
PubChem 6360 File:Yes check.svgY
ChemSpider 6120 File:Yes check.svgY
UNII BXR49TP611 File:Yes check.svgY
EC number 200-857-2
UN number 1969
KEGG D04623 File:Yes check.svgY
ChEBI CHEBI:30363 File:Yes check.svgY
RTECS number TZ4300000
Beilstein Reference 1730720
Gmelin Reference 1301
Jmol-3D images Image 1
Molecular formula C4H10
Molar mass 58.12 g mol−1
Exact mass 58.078250320 g mol−1
Appearance Colorless, transparent gas
Odor Odorless
Density 2.51 mg mL−1 (at 15 °C, 100 kPa)
Melting point

-233--33 °C, 40-240 K, -388--28 °F

Boiling point

-13--9 °C, 260-264 K, 8-16 °F

Vapor pressure 204.8 kPa (at 21 °C)
kH 8.6 nmol Pa−1 kg−1
Std enthalpy of
−134.8–−133.6 kJ mol−1
Std enthalpy of
−2.86959–−2.86841 MJ mol−1
Specific heat capacity, C 96.65 J K−1 mol−1
GHS pictograms Template:GHS flame
GHS signal word DANGER
GHS precautionary statements P210
EU Index 601-004-00-0
EU classification Template:Hazchem F+
R-phrases Template:R12
S-phrases Template:S2, Template:S16
NFPA 704
NFPA 704
Flash point -83 °C
460 °C
Explosive limits 1.4–8.3%
Related compounds
Related alkane Isopentane
 File:Yes check.svgY (verify) (what is: File:Yes check.svgY/Template:Cross?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Isobutane, also known as methylpropane, is an isomer of butane. It is the simplest alkane with a tertiary carbon. 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.[2]

Its UN number (for hazardous substances see shipping) is UN 1969.

Isobutane is the R group for the amino acid leucine.



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.[3]

Since the longest continuous chain in isobutane is only three carbon atoms, the systematic name is methylpropane. The position number (2-) is unnecessary because it is the only possibility in methylpropane.


  • As a refrigerant.[4]

The use in refrigerators started in 1993 when Greenpeace presented the Greenfreeze project with the German company Foron.[5]

Blends of pure, dry "isobutane" (R-600a) (commercial term used to describe isobutane mixtures) have negligible ozone depletion potential and very low Global Warming Potential (having a value of 3.3 times the GWP of carbon dioxide) and can serve as a functional replacement for R-12, R-22, R-134a, and other chlorofluorocarbon or hydrofluorocarbon refrigerants in conventional stationary refrigeration and air conditioning systems.

  • As a propellant for aerosol cans and foam products.

Safety Concerns[]

            Reports surfaced in late 2009 suggesting the use of isobutane as a refrigerant in domestic refrigerators was potentially dangerous. Several explosions resulting from the isobutane leaking into the refrigerator cabinet and a spark from the electrical system have been reported in the United Kingdom.[6] Although unclear how serious this could be, at the time this report came out it was estimated 300 million refrigerators worldwide use isobutane as a refrigerant.             Although these stories are only speculation, the use of a flammable gas as a refrigerant is quite dangerous and encompasses a great deal of risk. The normal risks a CFC or other toxic refrigerant would have when it escapes, are mainly related to depletion of breathable air and frosting at the point of escape. Isobutane has an explosion risk associated also (in addition to depletion of breathable air and frosting). This explosion risk is more dangerous directly to anyone in the vicinity should it accumulate and come into contact with any ignition source. To reduce the risk, the charge of refrigerators was reduced by more than 50% against R134a. The typical charge of a R600a freezer is 45g and of a refrigerator 20g. If 45g are lost at once, 1m³ of explosive gas can be created. The risk that all gas is lost outside in a short time is very low. For interior refrigeration applications, the R600a appliances should have a hidden condenser, so that the gas can not be lost. 20g is for example approximately 3-4 times the charge of a cigarette lighter. In Europe the limit is 150g for R600a appliances due to safety.             According to an MSDS (Material Safety Data Sheet) for isobutane, this gas should not be exposed to temperatures above 52 Celsius or 151 Fahrenheit while in a closed system such as a storage tank.[7] The range of flammability also factors into safety of this substance as a refrigerant. Flammable ranges for isobutane are between 1.8% - 8.4% and this creates a hazard when a leak forms in the refrigeration system. Many sources of ignition may be nearby so the unit could possibly explode due to the gas leak and cause major damage, not to mention injuries or death to persons nearby. This will create a problem for refrigeration technicians if a leak is reported. The leak must be checked in open air or well ventilated environments and the technician could risk injury to themselves or others. In essence, the refrigeration unit would need full replacement in most cases.           Substitution of this refrigerant for motor vehicle air conditioning systems not originally designed for R600a is widely prohibited or discouraged, on the grounds that using flammable hydrocarbons in systems originally designed to carry non-flammable refrigerant presents a significant risk of fire or explosion.[8][9][10][11][12][13][14][15]             Vendors and advocates of hydrocarbon refrigerants argue against such bans on the grounds that there have been very few such incidents relative to the number of vehicle air conditioning systems filled with hydrocarbons.[16][17] One particular test was conducted by a professor at the University of New South Wales that unintentionally tested the scenario of a sudden and complete refrigerant loss into the passenger compartment followed by subsequent ignition. He and several others in the car sustained burns to their face, ears, and hands, and several observers received lacerations from the burst glass of the front passenger window.[18]


  1. ISOBUTANE - Compound Summary. PubChem Compound. National Center for Biotechnology Information (16 September 2004). Retrieved on 5 March 2012.
  2. Patent Watch, July 31, 2006.
  3. Panico, R.; & Powell, W. H. (Eds.) (1994). "A Guide to IUPAC Nomenclature of Organic Compounds 1993".
  4. European Commission on retrofit refrigerants for stationary applications (PDF). Archived from the original on 2008-07-19. Retrieved on 2010-10-29.
  6. Template:Cite news
  8. U.S. EPA hydrocarbon-refrigerants FAQ. Retrieved on 2010-10-29.
  9. Compendium of hydrocarbon-refrigerant policy statements, October 2006Template:Dead link
  10. MACS bulletin: hydrocarbon refrigerant usage in vehicles (PDF). Retrieved on 2010-10-29.
  11. Society of Automotive Engineers hydrocarbon refrigerant bulletin. (2005-04-27). Retrieved on 2010-10-29.
  12. Shade Tree Mechanic on hydrocarbon refrigerants. (2005-04-27). Retrieved on 2010-10-29.
  13. Saskatchewan Labour bulletin on hydrocarbon refrigerants in vehicles. (2010-06-29). Retrieved on 2010-10-29.
  14. VASA on refrigerant legality & advisabilityTemplate:Dead link
  15. Queensland (Australia) government warning on hydrocarbon refrigerants. Archived from the original on 2008-12-17. Retrieved on 2010-10-29.
  16. New South Wales (Australia) Parliamentary record, 16 October 1997. (1997-10-16). Retrieved on 2010-10-29.
  17. New South Wales (Australia) Parliamentary record, 29 June 2000. Retrieved on 2010-10-29.
  18. VASA news report on hydrocarbon refrigerant demonstrationsTemplate:Dead link

External links[]