Pentene

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n-Pentene

1-Pentene

cis-2-Pentene

trans-2-Pentene
Names
IUPAC names
Pent-1-ene
cis-Pent-2-ene
trans-Pent-2-ene
Other names
amylene, n-amylene, n-pentene, beta-n-amylene, sym-methylethylethylene, pentylene
Identifiers
3D model (
JSmol
)
ChemSpider
ECHA InfoCard
 100.042.636 Edit this at Wikidata
EC Number
  • 246-916-6 (1-pentene)

    273-308-8 (cis-2-pentene)

    271-255-5 (trans-2-pentene)
UNII
  • (1-pentene): InChI=1S/C5H10/c1-3-5-4-2/h3H,1,4-5H2,2H3
    Key: YWAKXRMUMFPDSH-UHFFFAOYSA-N
  • (cis-2-pentene): InChI=1S/C5H10/c1-3-5-4-2/h3,5H,4H2,1-2H3/b5-3-
    Key: QMMOXUPEWRXHJS-HYXAFXHYSA-N
  • (trans-2-pentene): InChI=1S/C5H10/c1-3-5-4-2/h3,5H,4H2,1-2H3/b5-3+
    Key: QMMOXUPEWRXHJS-HWKANZROSA-N
  • (1-pentene): CCCC=C
  • (cis-2-pentene): CC/C=C\C
  • (trans-2-pentene): CC/C=C/C
Properties
C5H10
Molar mass 70.135 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]
-53.7·10−6 cm3/mol
Hazards
Safety data sheet (SDS) MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Pentenes (also called Pentylenes) are alkenes with the chemical formula C
5H
10. Each molecule contains one double bond within its molecular structure. Six different compounds are 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

thermal cracking of petroleum or during the production of ethylene and propylene
via thermal cracking of hydrocarbon fractions.

The only commercial manufacturer of 1-pentene is

Fischer-Tropsch process.[2]

2-Pentene has two geometric isomers: cis-2-pentene and trans-2-pentene. Cis-2-Pentene is used in olefin metathesis.

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 the three main byproducts of

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 DCC, which is operated very much like the FCC. Isobutylene and isoamylene feedstocks are necessary for the production of the much debated gasoline blending components methyl tert-butyl ether and tert-amyl methyl ether
.

Production of fuels

Propylene, isobutene, and amylenes are feedstocks in the alkylation units of refineries. Using isobutane, blendstocks are generated with high branching for good combustion characteristics. Amylenes are valued as precursors to fuels, especially aviation fuels of relatively low volatility, as required by various regulations.[3]

References

  1. ^ a b c Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health
  2. ^ "RSA Olefins | cChange". www.cchange.ac.za. Retrieved 2017-10-19.
  3. ISBN 0-471-23896-1
    .
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