2-Butene
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Names | |||
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IUPAC name
But-2-ene
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Other names
β-Butylene
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Identifiers | |||
107-01-7 590-18-1 (cis) 624-64-6 (trans) |
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ChEBI | CHEBI:48363 | ||
ChemSpider | 11719 4449912 (cis) 56442 (trans) |
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EC Number | 203-452-9 | ||
Jmol 3D model | Interactive image (cis): Interactive image (trans): Interactive image |
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PubChem | 5287573 (cis) 62695 (trans) |
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RTECS number | EM2932000 | ||
UNII | S1SK37516R | ||
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Properties | |||
C4H8 | |||
Molar mass | 56.106 g/mol | ||
Density | 0.641 g/mL (cis, at 3.7 °C)[1] 0.626 g/mL (trans, at 0.9 °C)[2] |
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Melting point | -138.9 ºC (cis)[1] -105.5 °C (trans)[2] |
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Boiling point | 3.7 ºC (cis)[1] 0.9 °C (trans)[2] |
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Vapor pressure | {{{value}}} | ||
Related compounds | |||
Related butenes
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1-Butene cis-2-Butene trans-2-Butene Isobutene |
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Related compounds
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Butane Butyne |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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verify (what is ?) | |||
Infobox references | |||
2-Butene is an acyclic alkene with four carbon atoms. It is the simplest alkene exhibiting cis/trans-isomerism (also known as (E/Z)-isomerism); that is, it exists as two geometric isomers cis-2-butene ((Z)-2-butene) and trans-2-butene ((E)-2-butene).
It is a petrochemical, produced by the catalytic cracking of crude oil or the dimerization of ethylene. Its main uses are in the production of gasoline (petrol) and butadiene,[3] although some 2-butene is also used to produce the solvent butanone via hydration to 2-butanol followed by oxidation.
The two isomers are extremely difficult to separate by distillation because of the proximity of their boiling points (~4 °C for cis and ~1 °C for trans[4]). However, separation is unnecessary in most industrial settings, as both isomers behave similarly in most of the desired reactions. A typical industrial 2-butene mixture is 70% (Z)-2-butene (cis-isomer) and 30% (E)-2-butene (trans-isomer). Butane and 1-butene are common impurities, present at 1% or more in industrial mixtures, which also contain smaller amounts of isobutene, butadiene and butyne.[3]
References
- ↑ 1.0 1.1 1.2 Record in the GESTIS Substance Database of the IFA
- ↑ 2.0 2.1 2.2 Record in the GESTIS Substance Database of the IFA
- ↑ 3.0 3.1 Lua error in package.lua at line 80: module 'strict' not found..
- ↑ Chemical Safety Information from Intergovernmental Organizations Archived December 9, 2009 at the Wayback Machine