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Showing metabocard for (E,E)-2,6-Octadienal (HMDB0039844)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 01:22:54 UTC
Update Date2023-02-21 17:27:15 UTC
HMDB IDHMDB0039844
Secondary Accession Numbers
  • HMDB39844
Metabolite Identification
Common Name(E,E)-2,6-Octadienal
Description(E,E)-2,6-Octadienal belongs to the class of organic compounds known as medium-chain aldehydes. These are an aldehyde with a chain length containing between 6 and 12 carbon atoms. Thus, (e,e)-2,6-octadienal is considered to be a fatty aldehyde (E,E)-2,6-Octadienal is a green tasting compound (E,E)-2,6-Octadienal has been detected, but not quantified in, fats and oils. This could make (e,e)-2,6-octadienal a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on (E,E)-2,6-Octadienal.
Structure
Data?1677000435
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0039844 ((E,E)-2,6-Octadienal)


  Mrv0541 02241217262D          

  9  8  0  0  0  0            999 V2000
   -2.8586   -0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1439    0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4292   -0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7146    0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4293   -0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1439    0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8586   -0.2061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
M  END
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3D MOL for HMDB0039844 ((E,E)-2,6-Octadienal)

HMDB0039844
     RDKit          3D
(E,E)-2,6-Octadienal
 21 20  0  0  0  0  0  0  0  0999 V2000
    3.3706    1.0518    0.3440 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5123    0.0622   -0.3606 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2000    0.2153   -0.5000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3588   -0.7948   -1.2131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7023   -1.3618   -0.2934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5511   -0.2159    0.1558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8460   -0.2199   -0.1191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6761    0.8971    0.3182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9009    0.8496    0.0342 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4021    0.6233    0.3751 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4522    2.0110   -0.2210 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9752    1.2844    1.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9229   -0.8587   -0.8084 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7449    1.1031   -0.0784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0966   -0.2682   -2.0777 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9436   -1.6307   -1.5981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2313   -1.8850    0.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3146   -2.1117   -0.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0971    0.5913    0.6937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2338   -1.0615   -0.6619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2329    1.7191    0.8619 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  1 10  1  0
  1 11  1  0
  1 12  1  0
  2 13  1  0
  3 14  1  0
  4 15  1  0
  4 16  1  0
  5 17  1  0
  5 18  1  0
  6 19  1  0
  7 20  1  0
  8 21  1  0
M  END
Download

3D SDF for HMDB0039844 ((E,E)-2,6-Octadienal)


  Mrv0541 02241217262D          

  9  8  0  0  0  0            999 V2000
   -2.8586   -0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1439    0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4292   -0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7146    0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4293   -0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1439    0.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8586   -0.2061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0039844

> <DATABASE_NAME>
hmdb

> <SMILES>
C\C=C\CC\C=C\C=O

> <INCHI_IDENTIFIER>
InChI=1S/C8H12O/c1-2-3-4-5-6-7-8-9/h2-3,6-8H,4-5H2,1H3/b3-2+,7-6+

> <INCHI_KEY>
CBXNRMOWVZUZQA-BLWKUPHCSA-N

> <FORMULA>
C8H12O

> <MOLECULAR_WEIGHT>
124.1803

> <EXACT_MASS>
124.088815006

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
15.004410393681354

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E,6E)-octa-2,6-dienal

> <ALOGPS_LOGP>
2.62

> <JCHEM_LOGP>
2.1773190383333336

> <ALOGPS_LOGS>
-2.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.231356240467496

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
41.5601

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.51e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E,6E)-octa-2,6-dienal

> <JCHEM_VEBER_RULE>
1

$$$$
Download

3D-SDF for HMDB0039844 ((E,E)-2,6-Octadienal)

HMDB0039844
     RDKit          3D
(E,E)-2,6-Octadienal
 21 20  0  0  0  0  0  0  0  0999 V2000
    3.3706    1.0518    0.3440 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5123    0.0622   -0.3606 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2000    0.2153   -0.5000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3588   -0.7948   -1.2131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7023   -1.3618   -0.2934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5511   -0.2159    0.1558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8460   -0.2199   -0.1191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6761    0.8971    0.3182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9009    0.8496    0.0342 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4021    0.6233    0.3751 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4522    2.0110   -0.2210 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9752    1.2844    1.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9229   -0.8587   -0.8084 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7449    1.1031   -0.0784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0966   -0.2682   -2.0777 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9436   -1.6307   -1.5981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2313   -1.8850    0.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3146   -2.1117   -0.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0971    0.5913    0.6937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2338   -1.0615   -0.6619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2329    1.7191    0.8619 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  1 10  1  0
  1 11  1  0
  1 12  1  0
  2 13  1  0
  3 14  1  0
  4 15  1  0
  4 16  1  0
  5 17  1  0
  5 18  1  0
  6 19  1  0
  7 20  1  0
  8 21  1  0
M  END
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PDB for HMDB0039844 ((E,E)-2,6-Octadienal)

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -5.336  -0.385   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.002   0.385   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.668  -0.385   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334   0.385   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -0.385   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334   0.385   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.668  -0.385   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.002   0.385   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.336  -0.385   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8                                                            
MASTER        0    0    0    0    0    0    0    0    9    0   16    0
END
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3D PDB for HMDB0039844 ((E,E)-2,6-Octadienal)

COMPND    HMDB0039844
HETATM    1  C1  UNL     1       3.371   1.052   0.344  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.512   0.062  -0.361  1.00  0.00           C  
HETATM    3  C3  UNL     1       1.200   0.215  -0.500  1.00  0.00           C  
HETATM    4  C4  UNL     1       0.359  -0.795  -1.213  1.00  0.00           C  
HETATM    5  C5  UNL     1      -0.702  -1.362  -0.293  1.00  0.00           C  
HETATM    6  C6  UNL     1      -1.551  -0.216   0.156  1.00  0.00           C  
HETATM    7  C7  UNL     1      -2.846  -0.220  -0.119  1.00  0.00           C  
HETATM    8  C8  UNL     1      -3.676   0.897   0.318  1.00  0.00           C  
HETATM    9  O1  UNL     1      -4.901   0.850   0.034  1.00  0.00           O  
HETATM   10  H1  UNL     1       4.402   0.623   0.375  1.00  0.00           H  
HETATM   11  H2  UNL     1       3.452   2.011  -0.221  1.00  0.00           H  
HETATM   12  H3  UNL     1       2.975   1.284   1.352  1.00  0.00           H  
HETATM   13  H4  UNL     1       2.923  -0.859  -0.808  1.00  0.00           H  
HETATM   14  H5  UNL     1       0.745   1.103  -0.078  1.00  0.00           H  
HETATM   15  H6  UNL     1      -0.097  -0.268  -2.078  1.00  0.00           H  
HETATM   16  H7  UNL     1       0.944  -1.631  -1.598  1.00  0.00           H  
HETATM   17  H8  UNL     1      -0.231  -1.885   0.564  1.00  0.00           H  
HETATM   18  H9  UNL     1      -1.315  -2.112  -0.830  1.00  0.00           H  
HETATM   19  H10 UNL     1      -1.097   0.591   0.694  1.00  0.00           H  
HETATM   20  H11 UNL     1      -3.234  -1.062  -0.662  1.00  0.00           H  
HETATM   21  H12 UNL     1      -3.233   1.719   0.862  1.00  0.00           H  
CONECT    1    2   10   11   12
CONECT    2    3    3   13
CONECT    3    4   14
CONECT    4    5   15   16
CONECT    5    6   17   18
CONECT    6    7    7   19
CONECT    7    8   20
CONECT    8    9    9   21
END
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SMILES for HMDB0039844 ((E,E)-2,6-Octadienal)

C\C=C\CC\C=C\C=O
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INCHI for HMDB0039844 ((E,E)-2,6-Octadienal)

InChI=1S/C8H12O/c1-2-3-4-5-6-7-8-9/h2-3,6-8H,4-5H2,1H3/b3-2+,7-6+
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View in JSmolView Stereo Labels
Synonyms
ValueSource
(2E,6E)-2,6-OctadienalHMDB
2,6-trans,trans-OctadienalHMDB
FEMA 3466HMDB
trans,trans-2,6-OctadienalHMDB
Chemical FormulaC8H12O
Average Molecular Weight124.1803
Monoisotopic Molecular Weight124.088815006
IUPAC Name(2E,6E)-octa-2,6-dienal
Traditional Name(2E,6E)-octa-2,6-dienal
CAS Registry Number56767-18-1
SMILES
C\C=C\CC\C=C\C=O
InChI Identifier
InChI=1S/C8H12O/c1-2-3-4-5-6-7-8-9/h2-3,6-8H,4-5H2,1H3/b3-2+,7-6+
InChI KeyCBXNRMOWVZUZQA-BLWKUPHCSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as medium-chain aldehydes. These are an aldehyde with a chain length containing between 6 and 12 carbon atoms.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbonyl compounds
Direct ParentMedium-chain aldehydes
Alternative Parents
Substituents
  • Medium-chain aldehyde
  • Enal
  • Alpha,beta-unsaturated aldehyde
  • Organic oxide
  • Hydrocarbon derivative
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
Physiological effect
Organoleptic effect
Disposition
Biological locationRoute of exposureSource
ProcessNot Available
Role
Biological roleIndustrial application
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling Point97.00 to 99.00 °C. @ 4.00 mm HgThe Good Scents Company Information System
Water Solubility951.7 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP2.064 (est)The Good Scents Company Information System
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.35 g/LALOGPS
logP2.62ALOGPS
logP2.18ChemAxon
logS-2.6ALOGPS
pKa (Strongest Basic)-4.2ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area17.07 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity41.56 m³·mol⁻¹ChemAxon
Polarizability15 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+130.93331661259
DarkChem[M-H]-127.59231661259
DeepCCS[M+H]+130.70730932474
DeepCCS[M-H]-128.51430932474
DeepCCS[M-2H]-164.80530932474
DeepCCS[M+Na]+139.62530932474
AllCCS[M+H]+128.932859911
AllCCS[M+H-H2O]+124.632859911
AllCCS[M+NH4]+132.932859911
AllCCS[M+Na]+134.132859911
AllCCS[M-H]-130.032859911
AllCCS[M+Na-2H]-132.632859911
AllCCS[M+HCOO]-135.532859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(E,E)-2,6-OctadienalC\C=C\CC\C=C\C=O1519.7Standard polar33892256
(E,E)-2,6-OctadienalC\C=C\CC\C=C\C=O1023.0Standard non polar33892256
(E,E)-2,6-OctadienalC\C=C\CC\C=C\C=O1054.6Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (E,E)-2,6-Octadienal GC-MS (Non-derivatized) - 70eV, Positivesplash10-0lfr-9000000000-fbb18e4deaf1d86267672017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (E,E)-2,6-Octadienal 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 - (E,E)-2,6-Octadienal 10V, Positive-QTOFsplash10-004i-3900000000-e0ce5782d92d3e4769642016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E,E)-2,6-Octadienal 20V, Positive-QTOFsplash10-056r-9600000000-15c180577ef889f0ab6f2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E,E)-2,6-Octadienal 40V, Positive-QTOFsplash10-1003-9000000000-7b09cdd106beee8d9be92016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E,E)-2,6-Octadienal 10V, Negative-QTOFsplash10-00di-0900000000-3a3a02888279cc2652a22016-08-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E,E)-2,6-Octadienal 20V, Negative-QTOFsplash10-00di-3900000000-047ba6f5589db3f1f8172016-08-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E,E)-2,6-Octadienal 40V, Negative-QTOFsplash10-0006-9100000000-13f49f40126dbbe9a2762016-08-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E,E)-2,6-Octadienal 10V, Positive-QTOFsplash10-0ar0-9000000000-f1bae51e30b1b1e7f6d92021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E,E)-2,6-Octadienal 20V, Positive-QTOFsplash10-0as0-9000000000-fcf60820264b90398b582021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E,E)-2,6-Octadienal 40V, Positive-QTOFsplash10-05r9-9000000000-27b41a2b6d6a77562f922021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E,E)-2,6-Octadienal 10V, Negative-QTOFsplash10-00di-1900000000-92909c7240ab40c70ab42021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E,E)-2,6-Octadienal 20V, Negative-QTOFsplash10-0a4l-6900000000-345020d0deb03fe525002021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E,E)-2,6-Octadienal 40V, Negative-QTOFsplash10-0gb9-9000000000-9e1c41f065d0fe16e1042021-09-22Wishart 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 IDFDB019498
KNApSAcK IDNot Available
Chemspider ID4896467
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound6365761
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1036351
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .