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Details

Stereochemistry ACHIRAL
Molecular Formula C8H14O
Molecular Weight 126.1962
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of 2-OCTENAL, (2E)-

SMILES

CCCCC\C=C\C=O

InChI

InChIKey=LVBXEMGDVWVTGY-VOTSOKGWSA-N
InChI=1S/C8H14O/c1-2-3-4-5-6-7-8-9/h6-8H,2-5H2,1H3/b7-6+

HIDE SMILES / InChI

Molecular Formula C8H14O
Molecular Weight 126.1962
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Study on the mechanisms of the antibacterial action of some plant alpha,beta-unsaturated aldehydes.
2002
Kairomone strains of Euclytiaflava (Townsend), a parasitoid of stink bugs.
2002 Aug
Chemical defense in the plant bug Lopidea robiniae (Uhler).
2002 Mar
Synthesis and biological evaluation of new citrate-based siderophores as potential probes for the mechanism of iron uptake in mycobacteria.
2002 May 9
Identification of the larval aggregation pheromone of codling moth, Cydia pomonella.
2005 Apr
Quantitative determination of volatile organic compounds in indoor dust using gas chromatography-UV spectrometry.
2005 Oct
Critical aspects of the determination of pentafluorobenzyl derivatives of aldehydes by gas chromatography with electron-capture or mass spectrometric detection: Validation of an optimized strategy for the determination of oxygen-related odor-active aldehydes in wine.
2006 Jul 28
Biosynthesis of C9-aldehydes in the moss Physcomitrella patens.
2006 Mar
Diastereoselective and enantiospecific synthesis of gamma-substituted alpha,beta-unsaturated nitriles from O-protected allylic cyanohydrins.
2006 May 12
In vitro antifungal and anti-elastase activity of some aliphatic aldehydes from Olea europaea L. fruit.
2006 Sep
Identification of volatile degradants in formulations containing sesame oil using SPME/GC/MS.
2007 Jun 28
Comparison of odor-active compounds from six distinctly different rice flavor types.
2008 Apr 23
Contribution of lipid oxidation products to acrylamide formation in model systems.
2008 Aug 13
Identification of the airborne aggregation pheromone of the common bed bug, Cimex lectularius.
2008 Jun
Influence of time, surface-to-volume ratio, and heating process (continuous or intermittent) on the emission rates of selected carbonyl compounds during thermal oxidation of palm and soybean oils.
2008 May 14
Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry.
2009 Apr 5
Effect of soybean volatile compounds on Aspergillus flavus growth and aflatoxin production.
2009 Mar
Effect of temperature on lipid-related volatile production in tomato puree.
2009 Oct 14
Formaldehyde in the indoor environment.
2010 Apr 14
A new method for the determination of carbonyl compounds in wines by headspace solid-phase microextraction coupled to gas chromatography-ion trap mass spectrometry.
2010 Dec 22
Cytotoxicity and genotoxicity in human lung epithelial A549 cells caused by airborne volatile organic compounds emitted from pine wood and oriented strand boards.
2010 Jun 16
4-oxo-aldehydes from the dorsal abdominal glands of the bed bug (Hemiptera: Cimicidae).
2010 Mar
Characterization of the antennal olfactory system of the bed bug (Cimex lectularius).
2010 Mar
Effect of enzyme activity and frozen storage on jalapeño pepper volatiles by selected ion flow tube-mass spectrometry.
2010 Nov-Dec
Neurotoxicity of fungal volatile organic compounds in Drosophila melanogaster.
2010 Oct
Exogenous methyl jasmonate diminishes the formation of lipid-derived compounds in boiled potato (Solanum tuberosum L.).
2010 Oct
Nymphs of the common bed bug (Cimex lectularius) produce anti-aphrodisiac defence against conspecific males.
2010 Sep 9
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:28:57 GMT 2023
Edited
by admin
on Fri Dec 15 17:28:57 GMT 2023
Record UNII
55N91D7775
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-OCTENAL, (2E)-
Systematic Name English
TRANS-2-OCTENAL
Systematic Name English
2-OCTENAL, (E)-
Systematic Name English
(E)-2-OCTEN-1-AL [FCC]
Common Name English
FEMA NO. 3215
Code English
2-OCTENAL [FHFI]
Common Name English
(E)-2-OCTENAL
Systematic Name English
(2E)-2-OCTENAL
Systematic Name English
(E)-OCT-2-ENAL
Systematic Name English
(E)-2-OCTEN-1-AL
FCC  
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION 2-OCTENAL
Created by admin on Fri Dec 15 17:28:57 GMT 2023 , Edited by admin on Fri Dec 15 17:28:57 GMT 2023
Code System Code Type Description
PUBCHEM
5283324
Created by admin on Fri Dec 15 17:28:57 GMT 2023 , Edited by admin on Fri Dec 15 17:28:57 GMT 2023
PRIMARY
CHEBI
61748
Created by admin on Fri Dec 15 17:28:57 GMT 2023 , Edited by admin on Fri Dec 15 17:28:57 GMT 2023
PRIMARY
CAS
2548-87-0
Created by admin on Fri Dec 15 17:28:57 GMT 2023 , Edited by admin on Fri Dec 15 17:28:57 GMT 2023
PRIMARY
JECFA MONOGRAPH
1362
Created by admin on Fri Dec 15 17:28:57 GMT 2023 , Edited by admin on Fri Dec 15 17:28:57 GMT 2023
PRIMARY
ECHA (EC/EINECS)
219-833-8
Created by admin on Fri Dec 15 17:28:57 GMT 2023 , Edited by admin on Fri Dec 15 17:28:57 GMT 2023
PRIMARY
FDA UNII
55N91D7775
Created by admin on Fri Dec 15 17:28:57 GMT 2023 , Edited by admin on Fri Dec 15 17:28:57 GMT 2023
PRIMARY
EPA CompTox
DTXSID40858789
Created by admin on Fri Dec 15 17:28:57 GMT 2023 , Edited by admin on Fri Dec 15 17:28:57 GMT 2023
PRIMARY