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Details

Stereochemistry ACHIRAL
Molecular Formula C10H18O
Molecular Weight 154.2493
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

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

SMILES

CCCCCCC\C=C\C=O

InChI

InChIKey=MMFCJPPRCYDLLZ-CMDGGOBGSA-N
InChI=1S/C10H18O/c1-2-3-4-5-6-7-8-9-10-11/h8-10H,2-7H2,1H3/b9-8+

HIDE SMILES / InChI

Molecular Formula C10H18O
Molecular Weight 154.2493
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Aroma components of an oil-based grill flavoring by direct thermal desorption-gas chromatography-olfactometry and sample dilution analysis.
2001
In vitro antibacterial activity of some aliphatic aldehydes from Olea europaea L.
2001 Apr 20
Mutagenicity and identification of mutagenic compounds of fumes obtained from heating peanut oil.
2001 Feb
Study on the mechanisms of the antibacterial action of some plant alpha,beta-unsaturated aldehydes.
2002
A novel, inducible, citral lyase purified from spores of Penicillium digitatum.
2002 Dec
Changes in volatile compounds of gamma-irradiated fresh cilantro leaves during cold storage.
2002 Dec 18
Sex attractant pheromone of the red-shouldered stink bug Thyanta pallidovirens: a pheromone blend with multiple redundant components.
2002 Sep
Volatile components in metatarsal glands of sika deer, Cervus nippon.
2003 Dec
Modes of antifungal action of (2E)-alkenals against Saccharomyces cerevisiae.
2003 Jul 2
Rapid assembly of the bicyclo[5.3.1]undecenone core of penostatin F: a successive Diels-Alder/Claisen reaction strategy with an efficient stereochemical relay.
2004 Apr 15
Cytotoxicity of diatom-derived oxylipins in organisms belonging to different phyla.
2004 Aug
Analysis of volatiles in porcine liver pâtés with added sage and rosemary essential oils by using SPME-GC-MS.
2004 Aug 11
The Hotdog fold: wrapping up a superfamily of thioesterases and dehydratases.
2004 Aug 12
Chemical and physical signals mediating conspecific and heterospecific aggregation behavior of first instar stink bugs.
2004 Jun
Application of solid-phase microextraction to the analysis of volatile compounds in virgin olive oils.
2004 Mar 5
Structural characterization of an etheno-2'-deoxyguanosine adduct modified by tetrahydrofuran.
2005 Feb
Identification of character-impact odorants in coriander and wild coriander leaves using gas chromatography-olfactometry (GCO) and comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry (GC x GC-TOFMS).
2005 Jun
Genotoxicity and oxidative stress of the mutagenic compounds formed in fumes of heated soybean oil, sunflower oil and lard.
2006 Jun
Characterization of epoxydecenal isomers as potent odorants in black tea (Dimbula) infusion.
2006 Jun 28
Changes induced by UV radiation during virgin olive oil storage.
2006 Jun 28
Qualitative study of organic compounds in wastewaters of a swine slaughterhouse.
2006 May
Ozone's impact on public health: contributions from indoor exposures to ozone and products of ozone-initiated chemistry.
2006 Oct
Inter- and intraspecific variation in defensive compounds produced by five neotropical stink bug species (Hemiptera: Pentatomidae).
2007 Jul
Identification of volatile degradants in formulations containing sesame oil using SPME/GC/MS.
2007 Jun 28
Differentiation of aroma characteristics of pine-mushrooms (Tricholoma matsutake Sing.) of different grades using gas chromatography-olfactometry and sensory analysis.
2007 Mar 21
Nematicidal activity of plant essential oils and components from coriander (Coriandrum sativum), Oriental sweetgum (Liquidambar orientalis), and valerian (Valeriana wallichii) essential oils against pine wood nematode (Bursaphelenchus xylophilus).
2008 Aug 27
Characterization of the most odor-active compounds in an American Bourbon whisky by application of the aroma extract dilution analysis.
2008 Jul 23
Potential chemosignals in the anogenital gland secretion of giant pandas, Ailuropoda melanoleuca, associated with sex and individual identity.
2008 Mar
Analysis of volatile compounds of Iberian dry-cured loins with different intramuscular fat contents using SPME-DED.
2008 May
Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry.
2009 Apr 5
Response of the egg parasitoids Trissolcus basalis and Telenomus podisi to compounds from defensive secretions of stink bugs.
2009 Jan
Exposure to polycyclic aromatic hydrocarbons (PAHs), mutagenic aldehydes and particulate matter during pan frying of beefsteak.
2010 Apr
A 13-Oxo-9,10-epoxytridecenoate phospholipid analogue of the genotoxic 4,5-epoxy-2E-decenal: detection in vivo, chemical synthesis, and adduction with DNA.
2010 Mar 15
Rhamnolipids: diversity of structures, microbial origins and roles.
2010 May
Changes in the key odorants of Italian Hazelnuts ( Coryllus avellana L. Var. Tonda Romana) induced by roasting.
2010 May 26
Biodiversity of volatile organic compounds from five French ferns.
2010 Oct
Identification of a lipid peroxidation product as the source of oxidation-specific epitopes recognized by anti-DNA autoantibodies.
2010 Oct 29
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:08:39 UTC 2023
Edited
by admin
on Fri Dec 15 17:08:39 UTC 2023
Record UNII
E93S23U2BU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-DECENAL, (2E)-
Systematic Name English
TRANS-2-DECEN-1-AL
Systematic Name English
2-DECENAL [FHFI]
Common Name English
2-DECENAL
FHFI  
Systematic Name English
FEMA NO. 2366
Code English
DECENALDEHYDE, TRANS-
Systematic Name English
(E)-2-DECENAL [FCC]
Common Name English
(2E)-2-DECENAL
Systematic Name English
NSC-20747
Code English
(E)-2-DECENAL
FCC  
Systematic Name English
DECENALDEHYDE
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION 2-DECENAL
Created by admin on Fri Dec 15 17:08:39 UTC 2023 , Edited by admin on Fri Dec 15 17:08:39 UTC 2023
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 17:08:39 UTC 2023 , Edited by admin on Fri Dec 15 17:08:39 UTC 2023
Code System Code Type Description
CAS
3913-81-3
Created by admin on Fri Dec 15 17:08:39 UTC 2023 , Edited by admin on Fri Dec 15 17:08:39 UTC 2023
PRIMARY
EPA CompTox
DTXSID5047035
Created by admin on Fri Dec 15 17:08:39 UTC 2023 , Edited by admin on Fri Dec 15 17:08:39 UTC 2023
PRIMARY
JECFA MONOGRAPH
1348
Created by admin on Fri Dec 15 17:08:39 UTC 2023 , Edited by admin on Fri Dec 15 17:08:39 UTC 2023
PRIMARY
ECHA (EC/EINECS)
223-472-1
Created by admin on Fri Dec 15 17:08:39 UTC 2023 , Edited by admin on Fri Dec 15 17:08:39 UTC 2023
NON-SPECIFIC STEREOCHEMISTRY
CHEBI
133455
Created by admin on Fri Dec 15 17:08:39 UTC 2023 , Edited by admin on Fri Dec 15 17:08:39 UTC 2023
PRIMARY
FDA UNII
E93S23U2BU
Created by admin on Fri Dec 15 17:08:39 UTC 2023 , Edited by admin on Fri Dec 15 17:08:39 UTC 2023
PRIMARY
PUBCHEM
5283345
Created by admin on Fri Dec 15 17:08:39 UTC 2023 , Edited by admin on Fri Dec 15 17:08:39 UTC 2023
PRIMARY
CHEBI
61727
Created by admin on Fri Dec 15 17:08:39 UTC 2023 , Edited by admin on Fri Dec 15 17:08:39 UTC 2023
PRIMARY
WIKIPEDIA
2-Decenal
Created by admin on Fri Dec 15 17:08:39 UTC 2023 , Edited by admin on Fri Dec 15 17:08:39 UTC 2023
PRIMARY
CAS
3913-71-1
Created by admin on Fri Dec 15 17:08:39 UTC 2023 , Edited by admin on Fri Dec 15 17:08:39 UTC 2023
NON-SPECIFIC STEREOCHEMISTRY
ECHA (EC/EINECS)
223-474-2
Created by admin on Fri Dec 15 17:08:39 UTC 2023 , Edited by admin on Fri Dec 15 17:08:39 UTC 2023
PRIMARY
NSC
20747
Created by admin on Fri Dec 15 17:08:39 UTC 2023 , Edited by admin on Fri Dec 15 17:08:39 UTC 2023
PRIMARY