Arachidyl alcohol
Skeletal formula of arachidyl alcohol
Spacefill model of arachidyl alcohol
Names
Preferred IUPAC name
Other names
Arachidalcohol
Arachidic alcohol
Hydroxyicosane
Icosalcohol
Icosanol
1-Icosanol
n -Icosanol
Icosyl alcohol
Icosyl hydrate
Icosylic alcohol
Nonadecylcarbinol
1-Eicosanol
Identifiers
CAS Number
3D model (JSmol)
Beilstein Reference
1705104
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard
100.010.110
EC Number
UNII
InChI=1S/C20H42O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21/h21H,2-20H2,1H3
Y Key: BTFJIXJJCSYFAL-UHFFFAOYSA-N
Y InChI=1/C20H42O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21/h21H,2-20H2,1H3
Key: BTFJIXJJCSYFAL-UHFFFAOYAC
CCCCCCCCCCCCCCCCCCCCO
OCCCCCCCCCCCCCCCCCCCC
Properties
Chemical formula
C 20 H 42 O
Molar mass
298.555 g·mol−1
Appearance
White, translucent crystals
Melting point
64 °C (147 °F; 337 K)
Boiling point
372 °C (702 °F; 645 K)
Solubility in water
1.51 × 10−6 g dm−3
log P
8.99
Vapor pressure
<0.01 kPa (at 20 °C)
Hazards
Flash point
195 °C (383 °F; 468 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Arachidyl alcohol (icosan-1-ol ), is a waxy substance used as an emollient in cosmetics. It is a straight-chain fatty alcohol with 20 carbon atoms, typically obtained via the hydrogenation of arachidic acid or arachidonic acid , both of which are present in peanut oil. Its name is derived from that of the peanut plant (Latin: arachis ).
References
^ "1-Eicosanol" . The PubChem Project . USA: National Center for Biotechnology Information.
Alcohols
By consumption
Alcohols found in alcoholic drinks Medical alcohol Toxic alcohols
Primary alcohols (1°)
Methanol
4-Methylcyclohexanemethanol
Aminomethanol
Cyclohexylmethanol
Methoxymethanol
Methylazoxymethanol
Trifluoromethanol
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
Amyl alcohols Aromatic alcohols Saturatedfatty alcohols Branched and unsaturatedfatty alcohols Sugar alcohols
C1 — C7 Deoxy sugar alcohols Cyclic sugar alcohols Glycylglycitols
Terpene alcohols
Monoterpene alcohols Sesquiterpene alcohols Diterpene alcohols
Dialcohols Trialcohols Sterols Fluoroalcohols Preparations
Substitution of haloalkane
Carbonyl reduction
Ether cleavage
Hydrolysis of epoxide
Hydration of alkene
Ziegler process
Reactions
Deprotonation
Protonation
Alcohol oxidation
Nucleophilic substitution
Fischer–Speier esterification
Williamson ether synthesis
Elimination reaction
Nucleophilic substitution of carbonyl group
Friedel-Crafts alkylation
Nucleophilic conjugate addition
Transesterification
Category