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Decene

Names
Preferred IUPAC name Dec-1-ene
Other names Alpha Olefin C10; Decylene; α-Decene; 1-decene
Identifiers
CAS Number	872-05-9 Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:87315
ChEMBL	ChEMBL3187990
ChemSpider	12809 Y
ECHA InfoCard	100.011.654
EC Number	212-819-2
PubChem CID	13381
RTECS number	HE2071401
UNII	7O4U4C718P Y
UN number	3295, 1993
CompTox Dashboard (EPA)	DTXSID8027329
InChI InChI=1S/C10H20/c1-3-5-7-9-10-8-6-4-2/h3H,1,4-10H2,2H3 Y Key: AFFLGGQVNFXPEV-UHFFFAOYSA-N Y InChI=1/C10H20/c1-3-5-7-9-10-8-6-4-2/h3H,1,4-10H2,2H3 Key: AFFLGGQVNFXPEV-UHFFFAOYAO
SMILES CCCCCCCCC=C
Properties
Chemical formula	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:
Pictograms
Signal word	Danger
Hazard statements	H226, H304, H410
Precautionary statements	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	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). Y verify (what is YN ?) Infobox references

Decene /dɛkiːn/ is an organic compound with the chemical formula C₁₀H₂₀. Decene contains a chain of ten carbon atoms with one double bond, making it an alkene. There are many isomers of decene depending on the position and geometry of the double bond. Dec-1-ene is the only isomer of industrial importance. As an alpha olefin, it is used as a comonomer 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 dec-1-ene are oligomerization of ethylene by the Ziegler process or by the cracking of petrochemical waxes.^[3]

In ethenolysis, methyl oleate, the methyl ester of oleic acid, converts to 1-decene and methyl 9-decenoate:^[4]

$\stackrel{\text{methyl oleate}}{CH{\phantom{A}}_3\left(CH{\phantom{A}}_2\right){\phantom{A}}_{7}CH=CH\left(CH{\phantom{A}}_2\right){\phantom{A}}_{7}CO{\phantom{A}}_{2}Me}+CH{\phantom{A}}_2=CH{\phantom{A}}_2⟶\stackrel{\text{1-decene}}{CH{\phantom{A}}_3\left(CH{\phantom{A}}_2\right){\phantom{A}}_{7}CH=CH{\phantom{A}}_2}+\stackrel{\text{9-decenoate}}{MeO{\phantom{A}}_{2}C\left(CH{\phantom{A}}_2\right){\phantom{A}}_{7}CH=CH{\phantom{A}}_2}$

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.

• Linstrom, Peter J.; Mallard, William G. (eds.). "Entry C872059". NIST Chemistry WebBook. NIST Standard Reference Database Number 69. Gaithersburg, Maryland: National Institute of Standards and Technology. doi:10.18434/T4D303.