Decene

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1-Decene
1-decene.svg
Dec-1-ene.svg
Names
IUPAC name
Dec-1-ene
Other names
Alpha Olefin C10; Decylene; α-Decene
Identifiers
872-05-9 YesY
ChemSpider 12809 YesY
Jmol 3D model Interactive image
UNII 7O4U4C718P YesY
  • InChI=1S/C10H20/c1-3-5-7-9-10-8-6-4-2/h3H,1,4-10H2,2H3 YesY
    Key: AFFLGGQVNFXPEV-UHFFFAOYSA-N YesY
  • InChI=1/C10H20/c1-3-5-7-9-10-8-6-4-2/h3H,1,4-10H2,2H3
    Key: AFFLGGQVNFXPEV-UHFFFAOYAO
  • CCCCCCCCC=C
Properties
C10H20
Molar mass 140.27 g·mol−1
Density 0.74 g/cm3[1]
Melting point −66.3 °C (−87.3 °F; 206.8 K)[1]
Boiling point 172 °C (342 °F; 445 K)[1]
Related compounds
Related Alkenes
Octene
Nonene
Undecene
Dodecene
Related compounds
Decane
Decanol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Decene /dɛkn/ is an alkene with the formula C
10
H
20
. Decene contains a chain of ten carbon atoms with one double bond. There are many isomers of decene depending on the position and geometry of the double bond. 1-Decene is the only isomer of industrial importance. As an alpha olefin, it is used as a monomer in copolymers and is an intermediate in the production of epoxides, amines, oxo alcohols, synthetic lubricants, synthetic fatty acids, and alkylated aromatics.[2]

The industrial processes used in the production of 1-decene are oligomerization of ethylene by the Ziegler Process or by the cracking of petrochemical waxes.[3]

1-Decene has been isolated from the leaves and rhizome of the plant Farfugium japonicum and has been detected as the initial product in the microbial degradation of n-decane.

References

  1. 1.0 1.1 1.2 Record in the GESTIS Substance Database of the IFA
  2. 1-Decene (Alpha Olefin C10), ineosoligomers.com
  3. Alfa Olefins, SIDS Initial Assessment Report

External links

  • Entry C872059 in Linstrom, P.J.; Mallard, W.G. (eds.) NIST Chemistry WebBook, NIST Standard Reference Database Number 69. National Institute of Standards and Technology, Gaithersburg MD. http://webbook.nist.gov