Chemistry:1-Nonene

1-Nonene
	; 1-Nonene
Names
	Preferred IUPAC name Non-1-ene
	Other names alpha-Nonene
Identifiers
CAS Number	124-11-8 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:77443 ;
ChemSpider	29025 ;
EC Number	271-212-0;
PubChem CID	31285;
UNII	YPK83LUD6G ;
UN number	1993
	InChI InChI=1S/C9H18/c1-3-5-7-9-8-6-4-2/h3H,1,4-9H2,2H3 Key: JRZJOMJEPLMPRA-UHFFFAOYSA-N ;
	SMILES 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 pictograms
GHS Signal word	Danger
GHS hazard statements	H226, H304, H315, H319, H335
GHS precautionary statements	P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P301+310, P302+352, P303+361+353, P304+340, P305+351+338, P312, P321, P331, P332+313, P337+313, P362, P370+378, P403+233, P403+235, P405
NFPA 704 (fire diamond)	3 0 0
Flash point	26 °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).
	verify (what is ?)
	Infobox references

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.

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Original source: https://en.wikipedia.org/wiki/1-Nonene. Read more

v t e Alkenes
Alkenes	Ethene ( C₂H₄ ) Propene ( C₃H₆ ) Butene ( C₄H₈ ) Pentene ( C₅H₁₀ ) Hexene ( C₆H₁₂ ) Heptene ( C₇H₁₄ ) Octene ( C₈H₁₆ ) Nonene ( C₉H₁₈ ) Decene ( C₁₀H₂₀ )
Preparations	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
Reactions	Hydrogenation Halogenation Hydration Electrophilic addition Oxymercuration reaction Hydroboration Cyclopropanation Epoxidation Dihydroxylation Ozonolysis Hydrohalogenation Polymerization Diels–Alder reaction Wacker process Dehydrogenation Ene reaction Friedel-Crafts Alkylation

Names
1-Nonene
Preferred IUPAC name Non-1-ene
Other names alpha-Nonene
Identifiers
CAS Number	124-11-8^Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:77443^Y
ChemSpider	29025^Y
EC Number	271-212-0
PubChem CID	31285
UNII	YPK83LUD6G^Y
UN number	1993
InChI InChI=1S/C9H18/c1-3-5-7-9-8-6-4-2/h3H,1,4-9H2,2H3^Y Key: JRZJOMJEPLMPRA-UHFFFAOYSA-N^Y
SMILES 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 pictograms
GHS Signal word	Danger
GHS hazard statements	H226, H304, H315, H319, H335
GHS precautionary statements	P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P301+310, P302+352, P303+361+353, P304+340, P305+351+338, P312, P321, P331, P332+313, P337+313, P362, P370+378, P403+233, P403+235, P405
NFPA 704 (fire diamond)	3 0 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 ^YN ?)
Infobox references