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Details

Stereochemistry RACEMIC
Molecular Formula C8H18O
Molecular Weight 130.2279
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-OCTANOL

SMILES

CCCCCCC(C)O

InChI

InChIKey=SJWFXCIHNDVPSH-UHFFFAOYSA-N
InChI=1S/C8H18O/c1-3-4-5-6-7-8(2)9/h8-9H,3-7H2,1-2H3

HIDE SMILES / InChI

Approval Year

2006
178
PubMed

PubMed

TitleDatePubMed
Solvent effect on ion-pair extraction of 2-(2-pyridylazo)-1-naphthol-4-sulfonate anion with solvated hydroxonium ion using alcohols and 1-octanol/octane mixed solvents.
2001 Feb
Stereocontrolled diels-alder cycloadditions of sugar-derived dihydropyranones with dienes.
2002 Nov 1
Regio- and enantioselective alkane hydroxylation with engineered cytochromes P450 BM-3.
2003 Nov 5
Photoswitching of ferroelectric liquid crystals using chiral thioindigo dopants: The development of a photochemical switch hitter.
2004
Studies on the mechanism of Indigo Carmine removal by solvent sublation.
2005 Dec 1
Role of histamine as a putative inhibitory transmitter in the honeybee antennal lobe.
2006 Dec 29
Understanding the logics of pheromone processing in the honeybee brain: from labeled-lines to across-fiber patterns.
2007
Retraction: (S)-(+)-2-octanol as a chiral oil core for the microemulsion electrokinetic chromatographic separation of chiral basic drugs [Anal. Sci., Vol. 23, p. 1071 (2007)].
2008 May
Telomerization of butadiene with glycerol: reaction control through process engineering, solvents, and additives.
2009
Intelligent chiral sensing based on supramolecular and interfacial concepts.
2010
Chromatography-olfactometry study of the aroma of fino sherry wines.
2010
Spontaneous product segregation from reactions in ionic liquids: application in Pd-catalyzed aliphatic alcohol oxidation.
2010 Feb 28
Effects of T-type calcium channel blockers on cocaine-induced hyperlocomotion and thalamocortical GABAergic abnormalities in mice.
2010 Oct
Patents

Patents

05294730
1
05476646
1
06998491
8
20010008869
4
JP2002537312A
3
JP2011500920A
2
JP3187838B2
5
Name Type Language
2-OCTANOL
FHFI   HSDB   MI  
Systematic Name English
S-OCTYL ALCOHOL
Common Name English
CAPRYL ALCOHOL
Common Name English
2-OCTANOL [FHFI]
Common Name English
N-OCTAN-2-OL
Common Name English
SEC-CAPRYLIC ALCOHOL
Common Name English
(RS)-2-OCTANOL
Systematic Name English
.BETA.-OCTYL ALCOHOL
Systematic Name English
1-METHYLHEPTANOL
Systematic Name English
2-OCTYL ALCOHOL
Systematic Name English
1-METHYL-1-HEPTANOL
Systematic Name English
NSC-14759
Code English
FEMA NO. 2801
Code English
DL-2-OCTANOL
Common Name English
1-METHYLHEPTYL ALCOHOL
Systematic Name English
DL-METHYLHEXYLCARBINOL
Common Name English
2-OCTANOL [HSDB]
Common Name English
2-HYDROXY-N-OCTANE
Common Name English
METHYLHEXYLCARBINOL
Systematic Name English
2-OCTANOL [MI]
Common Name English
HEXYLMETHYLCARBINOL
Systematic Name English
2-HYDROXYOCTANE
Systematic Name English
(±)-2-OCTANOL
Systematic Name English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
JECFA EVALUATION 2-OCTANOL
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
Code System Code Type Description
JECFA MONOGRAPH
395
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
SMS_ID
100000166333
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
CHEBI
37869
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-667-0
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
WIKIPEDIA
2-Octanol
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
PUBCHEM
20083
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
CAS
123-96-6
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
HSDB
5601
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
EVMPD
SUB180445
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
MESH
C067943
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
RXCUI
1362615
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY RxNorm
EPA CompTox
DTXSID0027014
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
CHEBI
16188
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
MERCK INDEX
m8111
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY Merck Index
NSC
14759
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
DAILYMED
66B0DD5E40
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
FDA UNII
66B0DD5E40
Created by admin on Fri Dec 15 17:52:51 GMT 2023 , Edited by admin on Fri Dec 15 17:52:51 GMT 2023
PRIMARY
SUBSTANCE RECORD
Structure of 2-OCTANOL
NIH
NCATS
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