Oleyl alcohol

Oleyl alcohol
Space-filling model of oleyl alcohol
Structural model of oleyl alcohol
Names
IUPAC name
(Z)-Octadec-9-en-1-ol
Other names
cis-9-Octadecen-1-ol
Identifiers
CAS Number
  • 143-28-2 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:73504 ☒N
ChemSpider
  • 4447562 checkY
ECHA InfoCard 100.005.089 Edit this at Wikidata
KEGG
  • D05245 checkY
PubChem CID
  • 5284499
UNII
  • 172F2WN8DV checkY
CompTox Dashboard (EPA)
  • DTXSID0022010 Edit this at Wikidata
InChI
  • InChI=1S/C18H36O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h9-10,19H,2-8,11-18H2,1H3/b10-9- checkY
    Key: ALSTYHKOOCGGFT-KTKRTIGZSA-N checkY
  • InChI=1/C18H36O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h9-10,19H,2-8,11-18H2,1H3/b10-9-
    Key: ALSTYHKOOCGGFT-KTKRTIGZBF
  • OCCCCCCCC\C=C/CCCCCCCC
Properties
Chemical formula
C18H36O
Molar mass 268.485 g·mol−1
Density 0.845-0.855 g/cm3
Melting point 13 to 19 °C (55 to 66 °F; 286 to 292 K)
Boiling point 330 to 360 °C (626 to 680 °F; 603 to 633 K)
Solubility in water
Insoluble
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
0
0
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

Oleyl alcohol /ˈliˌɪl, ˈliəl/,[1] or cis-9-octadecen-1-ol, is an unsaturated fatty alcohol with the molecular formula C18H36O or the condensed structural formula CH3(CH2)7−CH=CH−(CH2)8OH. It is a colorless oil, mainly used in cosmetics.[2]

It can be produced by the hydrogenation of oleic acid esters by Bouveault–Blanc reduction, which avoids reduction of the C=C group (as would occur with usual catalytic hydrogenation). The required oleate esters are obtained from beef fat, fish oil, and, in particular, olive oil (from which it gains its name). The original procedure was reported by Louis Bouveault in 1904[3] and subsequently refined.[4][5]

It has uses as a nonionic surfactant, emulsifier, emollient and thickener in skin creams, lotions and many other cosmetic products including shampoos and hair conditioners. It has also been investigated as a carrier for delivering medications through the skin or mucus membranes; particularly the lungs.[6]

See also

References

  1. ^ "Oleyl" in the McGraw–Hill Dictionary of Scientific & Technical Terms (2003)
  2. ^ 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.
  3. ^ Bouveault, L.; Blanc, G. (1904). "Hydrogénation des éthers des acides possédant en outre les fonctions éther-oxyde ou acétal" [Hydrogenation of the ether of the acids furthermore possessing the ether-oxide or acetal functions]. Bull. Soc. Chim. Fr. (in French). 31 (3): 1210–1213.
  4. ^ Reid, E. E.; Cockerille, F. O.; Meyer, J. D.; Cox, W. M.; Ruhoff, J. R. (1935). "Oleyl Alcohol". Organic Syntheses. 15: 51. doi:10.15227/orgsyn.015.0051; Collected Volumes, vol. 2, p. 468.
  5. ^ Adkins, Homer; Gillespie, R. H. (1935). "Oleyl alcohol". Org. Synth. 29: 51. doi:10.15227/orgsyn.015.0051.
  6. ^ Hussain, Alamdar; Arnold, John J.; Khan, Mansoor A.; Ahsan, Fakhrul (2004). "Absorption enhancers in pulmonary protein delivery". J. Control. Release. 94 (1): 15–24. doi:10.1016/j.jconrel.2003.10.001. PMID 14684268.
  • v
  • t
  • e
Alcohols
By consumption
Alcohols found in
alcoholic drinks
Medical alcohol
Toxic alcohols
Primary
alcohols (1°)
Methanol
Ethanol
Butanol
Straight-chain
saturated
C1 — C9
Straight-chain
saturated
C10 — C19
Straight-chain
saturated
C20 — C29
Straight-chain
saturated
C30 — C39
  • 1-Triacontanol (melissyl / myricyl)
  • 1-Hentriacontanol
  • 1-Dotriacontanol (lacceryl)
  • 1-Tritriacontanol
  • 1-Tetratriacontanol (geddyl)
  • 1-Pentatriacontanol
  • 1-Hexatriacontanol
  • 1-Heptatriacontanol
  • 1-Octatriacontanol
  • 1-Nonatriacontanol
Straight-chain
saturated
C40 — C49
  • 1-Tetracontanol
  • 1-Hentetracontanol
  • 1-Dotetracontanol
  • 1-Tritetracontanol
  • 1-Tetratetracontanol
  • 1-Pentatetracontanol
  • 1-Hexatetracontanol
  • 1-Heptatetracontanol
  • 1-Octatetracontanol
  • 1-Nonatetracontanol
Secondary
alcohols (2°)Tertiary
alcohols (3°)
Hydric alcohols
Monohydric alcohols
Dihydric alcohols
Trihydric alcohols
Polyhydric alcohols (sugar alcohols)
Amyl alcoholsAromatic alcoholsSaturated
fatty alcoholsBranched and
unsaturated
fatty alcohols
Sugar alcohols
C1 — C7
Deoxy sugar
alcohols
Cyclic sugar
alcohols
Glycylglycitols
Terpene alcohols
Monoterpene
alcohols
Sesquiterpene
alcohols
Diterpene
alcohols
DialcoholsTrialcoholsSterolsFluoroalcoholsPreparationsReactions
  • Category