Decene: Difference between revisions
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The industrial processes used in the production of 1-decene are [[oligomerization]] of [[ethylene]] by the [[Ziegler Process]] or by the [[Fluid catalytic cracking|cracking]] of petrochemical waxes.<ref>[http://www.inchem.org/documents/sids/sids/AOalfaolefins.pdf Alfa Olefins], SIDS Initial Assessment Report</ref> |
The industrial processes used in the production of 1-decene are [[oligomerization]] of [[ethylene]] by the [[Ziegler Process]] or by the [[Fluid catalytic cracking|cracking]] of petrochemical waxes.<ref>[http://www.inchem.org/documents/sids/sids/AOalfaolefins.pdf Alfa Olefins], SIDS Initial Assessment Report</ref> |
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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 |
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]]. |
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==References== |
==References== |
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Revision as of 08:17, 23 September 2015
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| Names | |
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| IUPAC name
Dec-1-ene
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| Other names
Alpha Olefin C10; Decylene; α-Decene
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.011.654 |
| UNII | |
CompTox Dashboard (EPA)
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| 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) |
| Boiling point | 172 °C (342 °F; 445 K) |
| Related compounds | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Decene /dɛkiːn/ is an alkene with the formula C
10H
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
- ^ a b c Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health
- ^ 1-Decene (Alpha Olefin C10), ineosoligomers.com
- ^ Alfa Olefins, SIDS Initial Assessment Report
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)