Isopentane
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Names | |
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IUPAC name
2-Methylbutane
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Other names
Methylbutane
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.001.039 |
RTECS number |
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C5H12 | |
Molar mass | 72.15 g/mol |
Appearance | colorless liquid |
Density | 0.616 g/ml, liquid[1] |
Melting point | −159.9 °C (113.3 K)[1] |
Boiling point | 27.7 °C (300.9 K)[1] |
Immiscible | |
Thermochemistry | |
Std molar
entropy (S⦵298) |
260.7 J·K−1·mol−1 |
Std enthalpy of
formation (ΔfH⦵298) |
−179 kJ/mol |
Std enthalpy of
combustion (ΔcH⦵298) |
−3504 kJ/mol |
Hazards | |
NFPA 704 (fire diamond) | |
Flash point | <−51 °C |
Explosive limits | 1.4–7.6% |
Related compounds | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Isopentane, C5H12, also called methylbutane or 2-methylbutane, is a branched-chain alkane with five carbon atoms. Isopentane is an extremely volatile and extremely flammable liquid at room temperature and pressure. The normal boiling point is just a few degrees above room temperature and isopentane will readily boil and evaporate away on a warm day. Isopentane is commonly used in conjunction with liquid nitrogen to achieve a liquid bath temperature of -160 °C.
An isopentyl group is a subset of the generic pentyl group. It has the chemical structure -CH3CH2CH(CH3)2.
Nomenclature
Isopentane is the name recommended by the International Union of Pure and Applied Chemistry (IUPAC) in its 1993 Recommendations for the Nomenclature of Organic Chemistry.[2] It is one of only four acyclic hydrocarbons to retain its pre-IUPAC name. An isopentyl group is a subset of the generic pentyl group. It has the chemical structure -CH3CH2CH(CH3)2.
Isomers
Isopentane is one of three structural isomers with the molecular formula C5H12, the others being pentane (n-pentane) and dimethyl propane (neopentane).
Uses
Isopentane is one of the ingredients in both Aquafresh® and Sensodyne®.[3]
References
- ^ a b c James Wei (1999), Molecular Symmetry, Rotational Entropy, and Elevated Melting Points. Ind. Eng. Chem. Res., volume 38 issue 12, pp. 5019–5027 {{doi:10.1021/ie990588m}}
- ^ 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) - ^ Aquafresh Website
External links
- International Chemical Safety Card 1153
- IUPAC Nomenclature of Organic Chemistry (online version of the "Blue Book")