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Details

Stereochemistry ACHIRAL
Molecular Formula C8H16O
Molecular Weight 128.212
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-OCTANONE

SMILES

CCCCCCC(C)=O

InChI

InChIKey=ZPVFWPFBNIEHGJ-UHFFFAOYSA-N
InChI=1S/C8H16O/c1-3-4-5-6-7-8(2)9/h3-7H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C8H16O
Molecular Weight 128.212
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Solvent free oxidation of primary alcohols and diols using thymine iron(III) catalyst.
2010-12-28
Parallel reinforcement pathways for conditioned food aversions in the honeybee.
2010-12-21
A molecular-structure hypothesis.
2010-11-01
Neurotoxicity of fungal volatile organic compounds in Drosophila melanogaster.
2010-10
Prolonged stimulus exposure reveals prolonged neurobehavioral response patterns.
2010-05-15
Purification and characterization of an anti-Prelog alcohol dehydrogenase from Oenococcus oeni that reduces 2-octanone to (R)-2-octanol.
2010-04
Hollow fiber-liquid-phase microextraction of fungicides from orange juices.
2010-03-26
Fragrance material review on methylheptenol.
2010-01
Memory formation in reversal learning of the honeybee.
2010
Multiple reversal olfactory learning in honeybees.
2010
t-3-Pentyl-r-2,c-6-diphenyl-piperidin-4-one.
2009-11-14
Is there a space-time continuum in olfaction?
2009-07
(E)-(2,4-Dichloro-phen-yl)[2-hydr-oxy-6-(methoxy-imino)cyclo-hex-1-en-yl]methanone.
2009-01-23
Differential odor processing in two olfactory pathways in the honeybee.
2009
Whole-cell bioreduction of aromatic alpha-keto esters using Candida tenuis xylose reductase and Candida boidinii formate dehydrogenase co-expressed in Escherichia coli.
2008-12-10
Selective three-phase liquid phase microextraction of acidic compounds from foodstuff simulants.
2008-07-11
Phthalate diesters and their metabolites in human breast milk, blood or serum, and urine as biomarkers of exposure in vulnerable populations.
2008-03
Generalization mediates sensitivity to complex odor features in the honeybee.
2008-02-27
Kinetic analysis of volatile formation in milk subjected to pressure-assisted thermal treatments.
2007-09
Predicting olfactory receptor neuron responses from odorant structure.
2007-05-04
Spectra and structure of binary azeotropes II. Acetone-n-pentane.
2007-01
Two polymorphs of potassium trichloro[diethyl (methylsulfinylmethyl)phosphonate-kappaS]platinum(II) with Z' = 1 and 3 in the space group P2(1)2(1)2(1).
2006-07
Anti-prelog reduction of prochiral carbonyl compounds by Oenococcus oeni in a biphasic system.
2006-07
Chemical boundaries for detection of eye irritation in humans from homologous vapors.
2006-06
Stability of immobilized soybean lipoxygenase in selected organic solvent media.
2005-10
Designing the "search pathway" in the development of a new class of highly efficient stereoselective hydrosilylation catalysts.
2005-04-22
Characterization of French and Spanish dry-cured hams: influence of the volatiles from the muscles and the subcutaneous fat quantified by SPME-GC.
2005-04
Perceptual and neural olfactory similarity in honeybees.
2005-04
Bimetallic isopropoxides M[Al(OC(3)H(i)(7))(4)](3) (M = Pr, Nd)--catalyzed reduction of 2-octanone and benzophenone.
2005-01-01
High-yield conversion of (R)-2-octanol from the corresponding racemate by stereoinversion using Candida rugosa.
2005-01
Controlled production of Camembert-type cheeses. Part II. Changes in the concentration of the more volatile compounds.
2004-08
Use of an ionic liquid in a two-phase system to improve an alcohol dehydrogenase catalysed reduction.
2004-05-07
Volatiles in a sausage surface model-influence of Penicillium nalgiovense, Pediococcus pentosaceus, ascorbate, nitrate and temperature.
2004-02
An efficient direct alpha-alkylation of ketones with primary alcohols catalyzed by [Ir(cod)Cl]2/PPh3/KOH system without solvent.
2004-01-14
Mass spectrometric analytical methods for the determination of endocrine disrupting chemicals (EDCs).
2004
Gas chromatography-olfactometry analysis of the volatile compounds of two commercial Irish beef meats.
2003-07-04
Associative learning of complex odours in parasitoid host location.
2003-03
Relationship between molecular structure, concentration and odor qualities of oxygenated aliphatic molecules.
2003-01
Analysis of ketones by selected ion flow tube mass spectrometry.
2003
Field dependence of mobilities for gas-phase-protonated monomers and proton-bound dimers of ketones by planar field asymmetric waveform ion mobility spectrometer (PFAIMS).
2002-06-06
Influence of lipid fraction, emulsifier fraction, and mean particle diameter of oil-in-water emulsions on the release of 20 aroma compounds.
2002-04-10
Asymmetric reduction of ketones with catecholborane using 2,6-BODOL complexes of titanium(IV) as catalysts.
2001-05-18
Interactions between artificial saliva and 20 aroma compounds in water and oil model systems.
2001-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:40:52 GMT 2025
Edited
by admin
on Mon Mar 31 18:40:52 GMT 2025
Record UNII
J2G84H29AF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-OCTANONE
FHFI   HSDB  
Systematic Name English
HEXYL METHYL KETONE
MI  
Preferred Name English
HEXYL METHYL KETONE [MI]
Common Name English
2-OCTANONE [FHFI]
Common Name English
METHYL N-HEXYL KETONE
Common Name English
2-OCTANONE [HSDB]
Common Name English
2-OXOOCTANE
Systematic Name English
METHYL HEXYL KETONE [FCC]
Common Name English
NSC-3712
Code English
FEMA NO. 2802
Code English
METHYL HEXYL KETONE
FCC  
Systematic Name English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 18:40:52 GMT 2025 , Edited by admin on Mon Mar 31 18:40:52 GMT 2025
JECFA EVALUATION 2-OCTANONE
Created by admin on Mon Mar 31 18:40:52 GMT 2025 , Edited by admin on Mon Mar 31 18:40:52 GMT 2025
Code System Code Type Description
CHEBI
87434
Created by admin on Mon Mar 31 18:40:52 GMT 2025 , Edited by admin on Mon Mar 31 18:40:52 GMT 2025
PRIMARY
PUBCHEM
8093
Created by admin on Mon Mar 31 18:40:52 GMT 2025 , Edited by admin on Mon Mar 31 18:40:52 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-837-1
Created by admin on Mon Mar 31 18:40:52 GMT 2025 , Edited by admin on Mon Mar 31 18:40:52 GMT 2025
PRIMARY
NSC
3712
Created by admin on Mon Mar 31 18:40:52 GMT 2025 , Edited by admin on Mon Mar 31 18:40:52 GMT 2025
PRIMARY
EPA CompTox
DTXSID4021927
Created by admin on Mon Mar 31 18:40:52 GMT 2025 , Edited by admin on Mon Mar 31 18:40:52 GMT 2025
PRIMARY
MERCK INDEX
m6017
Created by admin on Mon Mar 31 18:40:52 GMT 2025 , Edited by admin on Mon Mar 31 18:40:52 GMT 2025
PRIMARY Merck Index
MESH
C037075
Created by admin on Mon Mar 31 18:40:52 GMT 2025 , Edited by admin on Mon Mar 31 18:40:52 GMT 2025
PRIMARY
FDA UNII
J2G84H29AF
Created by admin on Mon Mar 31 18:40:52 GMT 2025 , Edited by admin on Mon Mar 31 18:40:52 GMT 2025
PRIMARY
JECFA MONOGRAPH
394
Created by admin on Mon Mar 31 18:40:52 GMT 2025 , Edited by admin on Mon Mar 31 18:40:52 GMT 2025
PRIMARY
HSDB
5545
Created by admin on Mon Mar 31 18:40:52 GMT 2025 , Edited by admin on Mon Mar 31 18:40:52 GMT 2025
PRIMARY
CAS
111-13-7
Created by admin on Mon Mar 31 18:40:52 GMT 2025 , Edited by admin on Mon Mar 31 18:40:52 GMT 2025
PRIMARY