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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 23:21:48 UTC
Update Date2023-02-21 17:26:21 UTC
HMDB IDHMDB0038079
Secondary Accession Numbers
  • HMDB38079
Metabolite Identification
Common Name(2E,6Z)-2,6-Nonadien-1-Yl acetate
Description(2E,6Z)-2,6-Nonadien-1-Yl acetate belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol. Based on a literature review a small amount of articles have been published on (2E,6Z)-2,6-Nonadien-1-Yl acetate.
Structure
Data?1677000381
Synonyms
ValueSource
(2E,6Z)-2,6-Nonadien-1-yl acetic acidGenerator
(2E,6Z)-Nona-2,6-dienyl acetateHMDB
1-Acetate(2E,6Z)-2,6-nonadien-1-olHMDB
2(e)-6(e)-Nonadienyl acetateHMDB
2-trans-6-cis-Nonadienyl acetateHMDB
Acetate(2E,6Z)-2,6-nonadien-1-olHMDB
Acetate(e,Z)-2,6-nonadien-1-olHMDB
FEMA 3952HMDB
Nonadienyl acetateHMDB
trans,cis-2,6-Nonadienyl acetateHMDB
trans-2,cis-6-Nonadienyl acetateHMDB
trans-2-cis-6-Nonadienyl acetateHMDB
(2Z,6Z)-Nona-2,6-dien-1-yl acetic acidGenerator
Chemical FormulaC11H18O2
Average Molecular Weight182.2594
Monoisotopic Molecular Weight182.13067982
IUPAC Name(2Z,6Z)-nona-2,6-dien-1-yl acetate
Traditional Name(2Z,6Z)-nona-2,6-dien-1-yl acetate
CAS Registry Number68555-65-7
SMILES
CC\C=C/CC\C=C/COC(C)=O
InChI Identifier
InChI=1S/C11H18O2/c1-3-4-5-6-7-8-9-10-13-11(2)12/h4-5,8-9H,3,6-7,10H2,1-2H3/b5-4-,9-8-
InChI KeyUHONGPVFPQQOSO-WPAMCMATSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassFatty Acyls
Sub ClassFatty alcohol esters
Direct ParentFatty alcohol esters
Alternative Parents
Substituents
  • Fatty alcohol ester
  • Carboxylic acid ester
  • Monocarboxylic acid or derivatives
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Physiological effect
Disposition
Process
Role
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling Point75.00 °C. @ 15.00 mm HgThe Good Scents Company Information System
Water Solubility26.5 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP3.531 (est)The Good Scents Company Information System
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.041 g/LALOGPS
logP3.69ALOGPS
logP2.9ChemAxon
logS-3.6ALOGPS
pKa (Strongest Basic)-7ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area26.3 ŲChemAxon
Rotatable Bond Count7ChemAxon
Refractivity56.37 m³·mol⁻¹ChemAxon
Polarizability21.38 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+147.35631661259
DarkChem[M-H]-142.45531661259
DeepCCS[M+H]+148.18330932474
DeepCCS[M-H]-144.49830932474
DeepCCS[M-2H]-181.61330932474
DeepCCS[M+Na]+157.24130932474
AllCCS[M+H]+145.032859911
AllCCS[M+H-H2O]+141.232859911
AllCCS[M+NH4]+148.632859911
AllCCS[M+Na]+149.732859911
AllCCS[M-H]-146.932859911
AllCCS[M+Na-2H]-148.432859911
AllCCS[M+HCOO]-150.232859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(2E,6Z)-2,6-Nonadien-1-Yl acetateCC\C=C/CC\C=C/COC(C)=O1721.8Standard polar33892256
(2E,6Z)-2,6-Nonadien-1-Yl acetateCC\C=C/CC\C=C/COC(C)=O1278.7Standard non polar33892256
(2E,6Z)-2,6-Nonadien-1-Yl acetateCC\C=C/CC\C=C/COC(C)=O1350.1Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate GC-MS (Non-derivatized) - 70eV, Positivesplash10-00kf-9300000000-e1e1ae1b2c1fd10f571d2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate 10V, Positive-QTOFsplash10-0089-1900000000-0427fd0557bf325676572017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate 20V, Positive-QTOFsplash10-00di-6900000000-a7023184b8a91e93f8192017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate 40V, Positive-QTOFsplash10-0f6x-9000000000-1ba049a187596852b6612017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate 10V, Negative-QTOFsplash10-001i-4900000000-54cbd39615f2439235c42017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate 20V, Negative-QTOFsplash10-0a4i-9300000000-cd961b4eaf9b5cec58f32017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate 40V, Negative-QTOFsplash10-0a4l-9200000000-24a23cb9676853a03ca22017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate 10V, Positive-QTOFsplash10-014l-9200000000-30051bd515afede550a32021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate 20V, Positive-QTOFsplash10-014i-9000000000-c320c1c0c4307e50de142021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate 40V, Positive-QTOFsplash10-014i-9000000000-5afb288fbc5d4b9c29182021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate 10V, Negative-QTOFsplash10-05fr-7900000000-6b2807686cdd4cdeeccd2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate 20V, Negative-QTOFsplash10-0a4i-9000000000-a3165501f6fc521f56e92021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2E,6Z)-2,6-Nonadien-1-Yl acetate 40V, Negative-QTOFsplash10-0a4i-9000000000-995316cfd01233c462442021-09-22Wishart LabView Spectrum

IR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)2023-02-04FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)2023-02-04FELIX labView Spectrum
Biological Properties
Cellular Locations
  • Membrane
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB017291
KNApSAcK IDNot Available
Chemspider ID30777231
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound124355621
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1047861
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
  2. Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
  3. Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
  4. Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
  5. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
  6. Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.