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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

Molecular Formula C8H18O
Molecular Weight 130.2279
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Enantioseparation of chiral amino acids as the N(O,S)-ethoxycarbonylated diastereomeric esters by achiral dual-capillary column gas chromatography.
2001 Dec
Synthesis of optically active 2-alkoxy-2H-pyran-3(6H)-ones. Their use as dienophiles in Diels-Alder cycloadditions.
2001 Dec 28
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
Effect of additives on electrokinetic properties of colloidal alumina suspension.
2002 Oct 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
Directed metalation route to ferroelectric liquid crystals with a chiral fluorenol core: the effect of restricted rotation on polar order.
2004 Feb 4
The stereoselectivity and catalytic properties of Xanthobacter autotrophicus 2-[(R)-2-Hydroxypropylthio]ethanesulfonate dehydrogenase are controlled by interactions between C-terminal arginine residues and the sulfonate of coenzyme M.
2004 Jun 1
The nature of the hydrophobic n-alkanol binding site within the C1 domains of protein kinase Calpha.
2004 Jun 15
General anesthetic octanol and related compounds activate wild-type and delF508 cystic fibrosis chloride channels.
2004 Mar
A hollow-fiber membrane extraction process for recovery and separation of lactic acid from aqueous solution.
2004 Spring
The effect of transdermal delivery of fentanyl on activity in growing pigs.
2005
Perceptual and neural olfactory similarity in honeybees.
2005 Apr
Studies on the mechanism of Indigo Carmine removal by solvent sublation.
2005 Dec 1
High-yield conversion of (R)-2-octanol from the corresponding racemate by stereoinversion using Candida rugosa.
2005 Jan
Role of histamine as a putative inhibitory transmitter in the honeybee antennal lobe.
2006 Dec 29
Effect of lipase immobilization on resolution of (R, S)-2-octanol in nonaqueous media using modified ultrastable-Y molecular sieve as support.
2006 Jul
Anti-prelog reduction of prochiral carbonyl compounds by Oenococcus oeni in a biphasic system.
2006 Jul
Core-shell type of nanoparticles composed of poly[(n-butyl cyanoacrylate)-co-(2-octyl cyanoacrylate)] copolymers for drug delivery application: synthesis, characterization and in vitro degradation.
2006 Nov 15
Functional characterization of alcohol oxidases from Aspergillus terreus MTCC 6324.
2006 Oct
Comparison of hydrogen bonding in 1-octanol and 2-octanol as probed by spectroscopic techniques.
2006 Sep 14
Hydrogen bonding in liquid and supercritical 1-octanol and 2-octanol assessed by near and midinfrared spectroscopy.
2006 Sep 7
Odor concentration invariance by chemical ratio coding.
2007
Understanding the logics of pheromone processing in the honeybee brain: from labeled-lines to across-fiber patterns.
2007
Determination of alcohol compounds using corona discharge ion mobility spectrometry.
2007
(S)-(+)-2-octanol as a chiral oil core for the microemulsion electrokinetic chromatographic separation of chiral basic drugs.
2007 Sep
Associative and non-associative plasticity in kenyon cells of the honeybee mushroom body.
2008
Deracemization of secondary alcohols through a concurrent tandem biocatalytic oxidation and reduction.
2008
Diastereoselective synthesis of (R)-(alkyl)-beta-D-galactopyranoside by using beta-galactosidase (Aspergillus oryzae) in low-water media.
2008 Jan 1
Activity of essential oils and individual components against acetyl- and butyrylcholinesterase.
2008 Jul-Aug
[Rapid determination of volatile flavor compounds in soy sauce using head space solid-phase microextraction and gas chromatography-mass spectrometry].
2008 May
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
Differential odor processing in two olfactory pathways in the honeybee.
2009
Telomerization of butadiene with glycerol: reaction control through process engineering, solvents, and additives.
2009
Optimization of poly(GMA-co-EDMA) monolithic support for trypsin nanoreactor fabrication.
2009 Jul
Intelligent chiral sensing based on supramolecular and interfacial concepts.
2010
Chromatography-olfactometry study of the aroma of fino sherry wines.
2010
Purification and characterization of an anti-Prelog alcohol dehydrogenase from Oenococcus oeni that reduces 2-octanone to (R)-2-octanol.
2010 Apr
Solvent free oxidation of primary alcohols and diols using thymine iron(III) catalyst.
2010 Dec 28
Calcium imaging in the ant Camponotus fellah reveals a conserved odour-similarity space in insects and mammals.
2010 Feb 26
Spontaneous product segregation from reactions in ionic liquids: application in Pd-catalyzed aliphatic alcohol oxidation.
2010 Feb 28
Energy transfer from silica core-surfactant shell nanoparticles to hosted molecular fluorophores.
2010 Nov 18
Effects of T-type calcium channel blockers on cocaine-induced hyperlocomotion and thalamocortical GABAergic abnormalities in mice.
2010 Oct
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:52:51 GMT 2023
Edited
by admin
on Fri Dec 15 17:52:51 GMT 2023
Record UNII
66B0DD5E40
Record Status Validated (UNII)
Record Version
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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
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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