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
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
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Enantioseparation of chiral amino acids as the N(O,S)-ethoxycarbonylated diastereomeric esters by achiral dual-capillary column gas chromatography. | 2001 Dec |
|
Efficient and selective microbial esterification with dry mycelium of Rhizopus oryzae. | 2001 Dec 14 |
|
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 |
|
Asymmetric reduction of ketones with catecholborane using 2,6-BODOL complexes of titanium(IV) as catalysts. | 2001 May 18 |
|
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 |
|
Photoinduced polarization inversion in a ferroelectric liquid crystal using an ambidextrous chiral thioindigo dopant. | 2003 Jun 11 |
|
On the mechanism of the unexpected facile formation of meso-diacetate products in enzymatic acetylation of alkanediols. | 2003 Mar 21 |
|
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 |
|
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 |
|
Role of histamine as a putative inhibitory transmitter in the honeybee antennal lobe. | 2006 Dec 29 |
|
Anti-prelog reduction of prochiral carbonyl compounds by Oenococcus oeni in a biphasic system. | 2006 Jul |
|
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 |
Name | Type | Language | ||
---|---|---|---|---|
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
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 | ||
---|---|---|---|---|---|
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | ||
|
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 | |||
|
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 | |||
|
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 | ||
|
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 | |||
|
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 | |||
|
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