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Details

Stereochemistry ACHIRAL
Molecular Formula C9H14O
Molecular Weight 138.2069
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of 2,6-NONADIENAL, (2E,6Z)-

SMILES

CC\C=C/CC\C=C\C=O

InChI

InChIKey=HZYHMHHBBBSGHB-ODYTWBPASA-N
InChI=1S/C9H14O/c1-2-3-4-5-6-7-8-9-10/h3-4,7-9H,2,5-6H2,1H3/b4-3-,8-7+

HIDE SMILES / InChI

Molecular Formula C9H14O
Molecular Weight 138.2069
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 2
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
DNA-damaging potential and glutathione depletion of 2-cyclohexene-1-one in mammalian cells, compared to food relevant 2-alkenals.
2001 Oct 18
Aroma components of cooked tail meat of American lobster (Homarus americanus).
2001 Sep
Solid-phase microextraction (SPME) technique for measurement of generation of fresh cucumber flavor compounds.
2001 Sep
Fresh cucumber flavor in refrigerated pickles: comparison of sensory and instrumental analysis.
2002 Aug 14
Important aroma compounds in freshly ground wholemeal and white wheat flour-identification and quantitative changes during sourdough fermentation.
2002 Nov 6
Aroma active components in aqueous kiwi fruit essence and kiwi fruit puree by GC-MS and multidimensional GC/GC-O.
2002 Sep 11
Tyrosinase inhibitory activity of cucumber compounds: enzymes responsible for browning in cucumber.
2003 Dec 17
Freshness assessments of Moroccan sardine (Sardina pilchardus): comparison of overall sensory changes to instrumentally determined volatiles.
2003 Dec 17
Determination of stale-flavor carbonyl compounds in beer by stir bar sorptive extraction with in-situ derivatization and thermal desorption-gas chromatography-mass spectrometry.
2003 Jan 31
Chemical and olfactometric characterization of volatile flavor compounds in a fish oil enriched milk emulsion.
2004 Jan 28
Relationship between intensity, concentration, and temperature for drinking water odorants.
2004 Mar
Modeling the sensory impact of defined combinations of volatile lipid oxidation products on fishy and metallic off-flavors.
2004 Mar 24
Determination of important odor-active aldehydes of wine through gas chromatography-mass spectrometry of their O-(2,3,4,5,6-pentafluorobenzyl)oximes formed directly in the solid phase extraction cartridge used for selective isolation.
2004 Mar 5
Inactivation of pathogenic bacteria by cucumber volatiles (E,Z)-2,6-nonadienal and (E)-2-nonenal.
2004 May
Characterization of the antioxidant activity of sugars and polyhydric alcohols in fish oil emulsions.
2004 Nov 17
Flavor characterization of ripened cod roe by gas chromatography, sensory analysis, and electronic nose.
2004 Oct 6
Determination of temperature-dependent Henry's law constants of odorous contaminants and their application to human perception.
2005 Jun 1
Impact of growing environment on chickasaw blackberry (Rubus L.) aroma evaluated by gas chromatography olfactometry dilution analysis.
2005 May 4
Characterization of dried whey protein concentrate and isolate flavor.
2005 Nov
Comparison of odor-active volatile compounds of fresh and smoked salmon.
2006 May 3
Instrumental and sensory characterization of heat-induced odorants in aseptically packaged soy milk.
2007 Apr 18
Characterization of the key aroma compounds in apricots (Prunus armeniaca) by application of the molecular sensory science concept.
2007 Jun 27
Comparison of three lychee cultivar odor profiles using gas chromatography-olfactometry and gas chromatography-sulfur detection.
2007 Mar 7
Plant volatile aldehydes as natural insecticides against stored-product beetles.
2008 Jan
Single-drop microextraction and gas chromatography-mass spectrometry for the determination of volatile aldehydes in fresh cucumbers.
2008 Jul
Aroma evaluation of transgenic, thaumatin II-producing cucumber fruits.
2009 Apr
Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry.
2009 Apr 5
Monitoring of autoxidation in LCPUFA-enriched lipid microparticles by electronic nose and SPME-GCMS.
2009 Jun 15
Identification and formation of volatile components responsible for the characteristic aroma of mat rush (igusa).
2010
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
Identification and quantification of impact aroma compounds in 4 nonfloral Vitis vinifera varieties grapes.
2010 Jan-Feb
Effect of enzyme activity and frozen storage on jalapeño pepper volatiles by selected ion flow tube-mass spectrometry.
2010 Nov-Dec
Substance Class Chemical
Created
by admin
on Sat Dec 16 20:17:08 GMT 2023
Edited
by admin
on Sat Dec 16 20:17:08 GMT 2023
Record UNII
93E895X03C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,6-NONADIENAL, (2E,6Z)-
Systematic Name English
(E),(Z)-2,6-NONADIENAL [FCC]
Common Name English
(E,Z)-2,6-NONADIEN-1-AL
Systematic Name English
2,6-NONADIENAL, (E,Z)-
Systematic Name English
NONADIENAL
INCI  
INCI  
Official Name English
(E),(Z)-2,6-NONADIENAL
FCC  
Common Name English
FEMA NO. 3377
Code English
NONADIENAL, 2-TRANS-6-CIS-
Common Name English
(2E,6Z)-NONA-2,6-DIENAL
Systematic Name English
(2E,6Z)-NONA-2,6-DIEN-1-AL
Systematic Name English
NONA-2-TRANS,-6-CIS-DIENAL [FHFI]
Common Name English
TRANS-2,CIS-6-NONADIENAL
Common Name English
VIOLET LEAF ALDEHYDE
Brand Name English
TRANS-2-CIS-6-NONADIENAL
Common Name English
NONADIENAL [INCI]
Common Name English
2,6-NONADIENAL, TRANS,CIS-
Systematic Name English
Code System Code Type Description
CHEBI
7610
Created by admin on Sat Dec 16 20:17:08 GMT 2023 , Edited by admin on Sat Dec 16 20:17:08 GMT 2023
PRIMARY
WIKIPEDIA
trans,cis-2,6-Nonadienal
Created by admin on Sat Dec 16 20:17:08 GMT 2023 , Edited by admin on Sat Dec 16 20:17:08 GMT 2023
PRIMARY
ECHA (EC/EINECS)
209-178-6
Created by admin on Sat Dec 16 20:17:08 GMT 2023 , Edited by admin on Sat Dec 16 20:17:08 GMT 2023
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JECFA MONOGRAPH
1177
Created by admin on Sat Dec 16 20:17:08 GMT 2023 , Edited by admin on Sat Dec 16 20:17:08 GMT 2023
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PUBCHEM
643731
Created by admin on Sat Dec 16 20:17:08 GMT 2023 , Edited by admin on Sat Dec 16 20:17:08 GMT 2023
PRIMARY
EPA CompTox
DTXSID1047104
Created by admin on Sat Dec 16 20:17:08 GMT 2023 , Edited by admin on Sat Dec 16 20:17:08 GMT 2023
PRIMARY
FDA UNII
93E895X03C
Created by admin on Sat Dec 16 20:17:08 GMT 2023 , Edited by admin on Sat Dec 16 20:17:08 GMT 2023
PRIMARY
CAS
557-48-2
Created by admin on Sat Dec 16 20:17:08 GMT 2023 , Edited by admin on Sat Dec 16 20:17:08 GMT 2023
PRIMARY