Nonene is an alkene with the molecular formula C9H18. Many structural isomers are possible, depending on the location of the C=C double bond and the branching of the other parts of the molecule. Industrially, the most important nonenes are trimers of propene: Tripropylene. This mixture of branched nonenes is used in the alkylation of phenol to produce nonylphenol, a precursor to detergents, which are also controversial pollutants.[1]
Linear nonenes
edit| Linear Nonene | ||||
| Name | 1-Nonene | 2-Nonene | 3-Nonene | 4-Nonene |
| Systematic name | Non-1-ene | Non-2-ene | Non-3-ene | Non-4-ene |
| Structure | 
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| CAS Number | 124-11-8 |
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| 27215-95-8 (all isomers) | ||||
| PubChem | CID 31285 from PubChem | CID 33744 from PubChem | CID 88350 from PubChem | CID 94226 from PubChem |
| Chemical formula | C9H18 | |||
| Molecular weight | 126.24 g·mol−1 | |||
| Melting point | −81 °C[2] | |||
| Boiling point | 147 °C[2] | 144–145 °C[3] | 147 °C[4] | |
| Density | 0,73 g·cm−3 (20 °C)[2] | 0,734 g·cm−3 (25 °C)[3] | 0,734 g·cm−3 (25 °C)[5] | 0,73 g·cm−3[4] |
| GHS hazard pictograms |    [2]
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[3]
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[5]
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[4]
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| GHS hazard statements | H226, H304, H315, H319, H335 | H226 | H226 | H226, H304 |
| P261, P301 P310, P305 P351 P338, P331 | P210, P233, P240, P241, P242, P243, P280, P301, P310 P303 P361 P353, P331, P370 P378, P403 P235, P405, P501 | |||
References
edit- ^ Fiege, H.; Voges, H. W.; Hamamoto, T.; Umemura, S.; Iwata, T.; Miki, H.; Fujita, Y.; Buysch, H. J.; Garbe, D. (2000-06-15). Phenol Derivatives. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA. pp. a19_313. doi:10.1002/14356007.a19_313. ISBN 978-3-527-30673-2. OCLC 46878292. Retrieved 2022-06-08.
{{cite book}}:|work=ignored (help) - ^ a b c d Record of 1-Nonen in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 1 February 2016.
- ^ a b c Sigma-Aldrich Co., trans-2-Nonen, 99%. Retrieved on 2 June 2017.
- ^ a b c Entry from 4-Nonene (cis- and trans-mixture) from TCI Europe, retrieved on 2 June 2017
- ^ a b Sigma-Aldrich Co., trans-3-Nonene, 99%. Retrieved on 2 June 2017.
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