Nonene

Not to be confused with nonane or nonyne.

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

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


CAS Number 124-11-8
  • 2216-38-8
  • 6434-77-1 (cis)
  • 6434-78-2 (trans)
  • 125146-82-9
  • 20237-46-1 (cis)
  • 20063-77-8 (trans)
  • 2198-23-4
  • 10405-84-2 (cis)
  • 10405-85-3 (trans)
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 GHS02: FlammableGHS08: Health hazardGHS07: Exclamation mark[2] GHS02: Flammable[3] GHS02: Flammable[5] GHS02: FlammableGHS08: Health hazard[4]
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

  1. ^ 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)
  2. ^ 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.
  3. ^ a b c Sigma-Aldrich Co., trans-2-Nonen, 99%. Retrieved on 2 June 2017.
  4. ^ a b c Entry from 4-Nonene (cis- and trans-mixture) from TCI Europe, retrieved on 2 June 2017
  5. ^ a b Sigma-Aldrich Co., trans-3-Nonene, 99%. Retrieved on 2 June 2017.
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