Pentene
 1-Pentene | |
 cis-2-Pentene | |
 trans-2-Pentene | |
| Identifiers | |
|---|---|
109-67-1 (1-pentene)  627-20-3 (cis-2-pentene) 646-04-8 (trans-2-pentene) | |
| 3D model (Jmol) | (1-pentene): Interactive image (cis-2-pentene): Interactive image (trans-2-pentene): Interactive image |
| ChemSpider | 7713 (1-pentene)  4483638 (cis-2-pentene) 4483639 (trans-2-pentene) |
| ECHA InfoCard | 100.042.636 |
| EC Number | 246-916-6 (1-pentene) 273-308-8 (cis-2-pentene) |
| PubChem | 8004 (1-pentene) 5326160 (cis-2-pentene) 5326161 (trans-2-pentene) |
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| Properties | |
| C5H10 | |
| Molar mass | 70.14 g·mol−1 |
| Density | 0.64 g/cm3 (1-pentene)[1] |
| Melting point | −165.2 °C (−265.4 °F; 108.0 K) (1-pentene)[1] |
| Boiling point | 30 °C (86 °F; 303 K) (1-pentene)[1] |
| Hazards | |
| Safety data sheet | MSDS |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| verify (what is ?) | |
| Infobox references | |
Pentenes are alkenes with chemical formula C
5H
10. Each contains one double bond within its molecular structure. There are a total of six different compounds in this class, differing from each other by whether the carbon atoms are attached linearly or in a branched structure, and whether the double bond has a cis or trans form.
Straight-chain isomers
1-Pentene is an alpha-olefin. Most often 1-pentene is made as a byproduct of catalytic or thermal cracking of petroleum, or during production of ethylene and propylene via thermal cracking of hydrocarbon fractions. It is rarely isolated as a separate compound. Instead, it is most often blended into gasoline or, in a mixture with other hydrocarbons, alkylated with isobutane to make gasoline.
The only commercial manufacturer of 1-pentene is Sasol Ltd, where it is separated from crude made by the Fischer-Tropsch process.
2-Pentene has two geometric isomers, cis-2-pentene and trans-2-pentene. cis-2-Pentene is used in olefin metathesis.
Alternative names for 1-pentene include amylene, n-amylene, and n-pentene. Alternative names for 2-pentene include beta-n-amylene and sym-methylethylethylene.
Branched-chain isomers
The branched isomers are 2-methylbut-1-ene, 3-methylbut-1-ene (isopentene), and 2-methylbut-2-ene (isoamylene).
Isoamylene is one of three main byproducts of deep catalytic cracking (DCC), a relatively new concept that is very similar to the operation of the fluid catalytic cracking (FCC). The DCC uses vacuum gas oil (VGO) as a feedstock to produce primarily propylene, isobutylene, and isoamylene. The rise in demand for polypropylene has encouraged the growth of the DCCU, which is operated very much like an FCCU. Isobutylene and isoamylene are feedstocks necessary for the production of the much debated gasoline blending components methyl tert-butyl ether (MTBE) and tert-amyl methyl ether (TAME).
See also
References
| Alkali metal hydrides |  Lithium hydride, LiH ionic metal hydride   Beryllium hydride Left (gas phase): BeH2 covalent metal hydride Right: (BeH2)n (solid phase) polymeric metal hydride   Borane and diborane Left: BH3 (special conditions), covalent metalloid hydride Right: B2H6 (standard conditions), dimeric metalloid hydride  Methane, CH4 covalent nonmetal hydride  Ammonia, NH3 covalent nonmetal hydride  Water, H2O covalent nonmetal hydride  Hydrogen fluoride, HF covalent nonmetal hydride | ||||||||||||||||||
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| Alkaline earth hydrides |
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| Group 13 hydrides |
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| Group 14 hydrides |
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| Pnictogen hydrides |
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| Hydrogen chalcogenides |
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| Hydrogen halides | |||||||||||||||||||
| Transition metal hydrides | |||||||||||||||||||
| Lanthanide hydrides |
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| Actinide hydrides |
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