Linoleyl alcohol

Linoleyl alcohol
Names
	Preferred IUPAC name (9Z,12Z)-Octadeca-9,12-dien-1-ol
Identifiers
CAS Number	506-43-4 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:73534 ;
ChemSpider	4517641 ;
ECHA InfoCard	100.007.308
EC Number	208-038-1;
PubChem CID	5365682;
UNII	P4OX1289YW ;
CompTox Dashboard (EPA)	DTXSID50881240 ;
	InChI InChI=1S/C18H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h6-7,9-10,19H,2-5,8,11-18H2,1H3/b7-6-,10-9- Key: JXNPEDYJTDQORS-HZJYTTRNSA-N ;
	SMILES CCCCC/C=C\C/C=C\CCCCCCCCO;
Properties
Chemical formula	C18H34O
Molar mass	266.469 g·mol−1
Appearance	colorless oil
Density	0.8612 g/cm3
Boiling point	153-4 0.4 kPa
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). verify (what is ?) Infobox references

Linoleyl alcohol is a fatty alcohol.^[1] A colorless oil, it is produced by the reduction of the carboxylic acid group in linoleic acid.^[2]

References

^ Noweck, Klaus; Grafahrend, Wolfgang (2006). "Fatty Alcohols". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_277.pub2. ISBN 978-3527306732.
^ Adkins, Homer; Gillespie, R. H. (1949). "Oleyl Alcohol". Organic Syntheses. 29: 80. doi:10.15227/orgsyn.029.0080.

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[Ullmann-1] Noweck, Klaus; Grafahrend, Wolfgang (2006). "Fatty Alcohols". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_277.pub2. ISBN 978-3527306732.

[2] Adkins, Homer; Gillespie, R. H. (1949). "Oleyl Alcohol". Organic Syntheses. 29: 80. doi:10.15227/orgsyn.029.0080.

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