Decene

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Decene
Names
Preferred IUPAC name
Dec-1-ene
Other names
Alpha Olefin C10; Decylene; α-Decene; 1-decene
Identifiers
3D model (
JSmol
)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard
100.011.654 Edit this at Wikidata
EC Number
  • 212-819-2
RTECS number
  • HE2071401
UNII
UN number 3295, 1993
  • InChI=1S/C10H20/c1-3-5-7-9-10-8-6-4-2/h3H,1,4-10H2,2H3 checkY
    Key: AFFLGGQVNFXPEV-UHFFFAOYSA-N checkY
  • 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 140.270 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]
Hazards
GHS labelling:
GHS02: FlammableGHS08: Health hazardGHS09: Environmental hazard
Danger
H226, H304, H410
P210, P233, P240, P241, P242, P243, P273, P280, P301+P310, P303+P361+P353, P331, P370+P378, P391, P403+P235, P405, P501
Related compounds
Related Alkenes
Dodecene
Related compounds
Decanol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Decene

aromatics.[2]

The industrial processes used in the production of dec-1-ene are

oligomerization of ethylene by the Ziegler process or by the cracking of petrochemical waxes.[3]

In

1-decene and methyl 9-decenoate:[4]

Dec-1-ene 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

External links

  • Entry C872059 in Linstrom, Peter J.; Mallard, William G. (eds.); NIST Chemistry WebBook, NIST Standard Reference Database Number 69, National Institute of Standards and Technology, Gaithersburg (MD)
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