1-Nonene

1-Nonene

1-Nonene
Names
Preferred IUPAC name
Non-1-ene
Other names
alpha-Nonene
Identifiers
CAS Number
  • 124-11-8 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:77443 checkY
ChemSpider
  • 29025 checkY
ECHA InfoCard 100.004.257 Edit this at Wikidata
EC Number
  • 271-212-0
PubChem CID
  • 31285
UNII
  • YPK83LUD6G checkY
UN number 1993
CompTox Dashboard (EPA)
  • DTXSID2059562 Edit this at Wikidata
InChI
  • InChI=1S/C9H18/c1-3-5-7-9-8-6-4-2/h3H,1,4-9H2,2H3 checkY
    Key: JRZJOMJEPLMPRA-UHFFFAOYSA-N checkY
  • C=C\CCCCCCC
Properties
Chemical formula
 C9H18
Molar mass 126.243 g·mol−1
Appearance Colorless liquid
Odor Onion-like, grassy
Density 0.7433 g/cm3
Melting point −81.3 °C (−114.3 °F; 191.8 K)
Boiling point 146.9 °C (296.4 °F; 420.0 K)
Solubility in water
 Insoluble
Solubility in other solvents Soluble in alcohol
Hazards
GHS labelling:
Pictograms
 GHS02: FlammableGHS07: Exclamation markGHS08: Health hazard
Danger
H226, H304, H315, H319, H335
P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P301+P310, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P312, P321, P331, P332+P313, P337+P313, P362, P370+P378, P403+P233, P403+P235, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chlorideFlammability 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasolineInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
0
3
0
Flash point 26[1] °C (79 °F; 299 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references
Chemical compound

1-Nonene is particular structural isomer of nonene where the double bond is located at the primary, or alpha, position making it a linear alpha olefin. It is used in the production of surfactants and lubricants, usually by way of nonylphenol. Its more branched analogue, tripropylene, is also used in this way.

References

  1. ^ "NFPA Hazard Rating Information for Common Chemicals". Archived from the original on 2015-02-17. Retrieved 2015-03-13.
  • v
  • t
  • e
Alkenes
PreparationsReactions
Stub icon

This article about an alkene is a stub. You can help Wikipedia by expanding it.

  • v
  • t
  • e
Stub icon

This article about a hydrocarbon is a stub. You can help Wikipedia by expanding it.

  • v
  • t
  • e