1-Nonene
![]() 1-Nonene | |
Names | |
---|---|
Preferred IUPAC name Non-1-ene | |
Other names alpha-Nonene | |
Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
ChEBI |
|
ChemSpider |
|
ECHA InfoCard | 100.004.257 ![]() |
EC Number |
|
PubChem CID |
|
UNII |
|
UN number | 1993 |
CompTox Dashboard (EPA) |
|
InChI
| |
| |
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 | ![]() ![]() ![]() |
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) | ![]() 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). ![]() ![]() ![]() 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
- ^ "NFPA Hazard Rating Information for Common Chemicals". Archived from the original on 2015-02-17. Retrieved 2015-03-13.
- v
- t
- e
- Dehydrohalogenation from haloalkane
- Dehydration reaction from alcohol
- Semihydrogenation from alkyne
- Bamford–Stevens reaction
- Barton–Kellogg reaction
- Boord olefin synthesis
- Chugaev elimination
- Cope reaction
- Corey–Winter olefin synthesis
- Grieco elimination
- Hofmann elimination
- Horner–Wadsworth–Emmons reaction
- Hydrazone iodination
- Julia olefination
- Kauffmann olefination
- McMurry reaction
- Peterson olefination
- Ramberg–Bäcklund reaction
- Shapiro reaction
- Takai olefination
- Wittig reaction
- Olefin metathesis
- Ene reaction
- Cope rearrangement
![]() | This article about an alkene is a stub. You can help Wikipedia by expanding it. |
- v
- t
- e
![]() | This article about a hydrocarbon is a stub. You can help Wikipedia by expanding it. |
- v
- t
- e