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Showing metabocard for 2,6-Dibromophenol (HMDB0032080)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 17:47:39 UTC
Update Date2022-03-07 02:53:14 UTC
HMDB IDHMDB0032080
Secondary Accession Numbers
  • HMDB32080
Metabolite Identification
Common Name2,6-Dibromophenol
Description2,6-Dibromophenol, also known as 2,6-DBP, belongs to the class of organic compounds known as o-bromophenols. These are bromophenols carrying a iodine at the C2 position of the benzene ring. 2,6-Dibromophenol is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. Based on a literature review a significant number of articles have been published on 2,6-Dibromophenol.
Structure
Data?1563862215
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0032080 (2,6-Dibromophenol)


  Mrv0541 05061306202D          

  9  9  0  0  0  0            999 V2000
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  2  0  0  0  0
  6  4  2  0  0  0  0
  6  5  1  0  0  0  0
  7  4  1  0  0  0  0
  8  5  1  0  0  0  0
  9  6  1  0  0  0  0
M  END
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3D MOL for HMDB0032080 (2,6-Dibromophenol)

HMDB0032080
     RDKit          3D
2,6-Dibromophenol
 13 13  0  0  0  0  0  0  0  0999 V2000
    2.1650    1.1038    0.0670 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9455    0.4452    0.0257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2275    1.1655    0.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2072    3.0850    0.3062 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -1.4243    0.4828    0.0743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4684   -0.8885   -0.0592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2889   -1.5954   -0.1508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9222   -0.9282   -0.1084 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5319   -1.9535   -0.2394 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.1924    2.1084    0.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3499    1.0370    0.1462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4340   -1.3944   -0.0904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3568   -2.6679   -0.2546 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8  2  1  0
  1 10  1  0
  5 11  1  0
  6 12  1  0
  7 13  1  0
M  END
Download

3D SDF for HMDB0032080 (2,6-Dibromophenol)


  Mrv0541 05061306202D          

  9  9  0  0  0  0            999 V2000
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  2  0  0  0  0
  6  4  2  0  0  0  0
  6  5  1  0  0  0  0
  7  4  1  0  0  0  0
  8  5  1  0  0  0  0
  9  6  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0032080

> <DATABASE_NAME>
hmdb

> <SMILES>
OC1=C(Br)C=CC=C1Br

> <INCHI_IDENTIFIER>
InChI=1S/C6H4Br2O/c7-4-2-1-3-5(8)6(4)9/h1-3,9H

> <INCHI_KEY>
SSIZLKDLDKIHEV-UHFFFAOYSA-N

> <FORMULA>
C6H4Br2O

> <MOLECULAR_WEIGHT>
251.903

> <EXACT_MASS>
249.862890044

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
16.38871041164723

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,6-dibromophenol

> <ALOGPS_LOGP>
3.43

> <JCHEM_LOGP>
3.2071857449999994

> <ALOGPS_LOGS>
-2.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.789530853096006

> <JCHEM_PKA_STRONGEST_BASIC>
-7.398327732761804

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
43.284499999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.04e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,6-dibromophenol

> <JCHEM_VEBER_RULE>
1

$$$$
Download

3D-SDF for HMDB0032080 (2,6-Dibromophenol)

HMDB0032080
     RDKit          3D
2,6-Dibromophenol
 13 13  0  0  0  0  0  0  0  0999 V2000
    2.1650    1.1038    0.0670 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9455    0.4452    0.0257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2275    1.1655    0.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2072    3.0850    0.3062 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -1.4243    0.4828    0.0743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4684   -0.8885   -0.0592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2889   -1.5954   -0.1508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9222   -0.9282   -0.1084 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5319   -1.9535   -0.2394 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.1924    2.1084    0.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3499    1.0370    0.1462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4340   -1.3944   -0.0904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3568   -2.6679   -0.2546 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8  2  1  0
  1 10  1  0
  5 11  1  0
  6 12  1  0
  7 13  1  0
M  END
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PDB for HMDB0032080 (2,6-Dibromophenol)

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    7 Br   UNK     0       1.334   3.850   0.000  0.00  0.00          Br+0
HETATM    8 Br   UNK     0      -1.334  -0.770   0.000  0.00  0.00          Br+0
HETATM    9  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    2    3                                                       
CONECT    2    1    4                                                       
CONECT    3    1    5                                                       
CONECT    4    2    6    7                                                  
CONECT    5    3    6    8                                                  
CONECT    6    4    5    9                                                  
CONECT    7    4                                                            
CONECT    8    5                                                            
CONECT    9    6                                                            
MASTER        0    0    0    0    0    0    0    0    9    0   18    0
END
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3D PDB for HMDB0032080 (2,6-Dibromophenol)

COMPND    HMDB0032080
HETATM    1  O1  UNL     1       2.165   1.104   0.067  1.00  0.00           O  
HETATM    2  C1  UNL     1       0.945   0.445   0.026  1.00  0.00           C  
HETATM    3  C2  UNL     1      -0.228   1.166   0.119  1.00  0.00           C  
HETATM    4 BR1  UNL     1      -0.207   3.085   0.306  1.00  0.00          BR  
HETATM    5  C3  UNL     1      -1.424   0.483   0.074  1.00  0.00           C  
HETATM    6  C4  UNL     1      -1.468  -0.888  -0.059  1.00  0.00           C  
HETATM    7  C5  UNL     1      -0.289  -1.595  -0.151  1.00  0.00           C  
HETATM    8  C6  UNL     1       0.922  -0.928  -0.108  1.00  0.00           C  
HETATM    9 BR2  UNL     1       2.532  -1.953  -0.239  1.00  0.00          BR  
HETATM   10  H1  UNL     1       2.192   2.108   0.165  1.00  0.00           H  
HETATM   11  H2  UNL     1      -2.350   1.037   0.146  1.00  0.00           H  
HETATM   12  H3  UNL     1      -2.434  -1.394  -0.090  1.00  0.00           H  
HETATM   13  H4  UNL     1      -0.357  -2.668  -0.255  1.00  0.00           H  
CONECT    1    2   10
CONECT    2    3    3    8
CONECT    3    4    5
CONECT    5    6    6   11
CONECT    6    7   12
CONECT    7    8    8   13
CONECT    8    9
END
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SMILES for HMDB0032080 (2,6-Dibromophenol)

OC1=C(Br)C=CC=C1Br
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INCHI for HMDB0032080 (2,6-Dibromophenol)

InChI=1S/C6H4Br2O/c7-4-2-1-3-5(8)6(4)9/h1-3,9H
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View in JSmolView Stereo Labels
Synonyms
ValueSource
26-Dibromo-phenolHMDB
2,6-Dibromo-phenolHMDB
2,6-DBPHMDB
Chemical FormulaC6H4Br2O
Average Molecular Weight251.903
Monoisotopic Molecular Weight249.862890044
IUPAC Name2,6-dibromophenol
Traditional Name2,6-dibromophenol
CAS Registry Number608-33-3
SMILES
OC1=C(Br)C=CC=C1Br
InChI Identifier
InChI=1S/C6H4Br2O/c7-4-2-1-3-5(8)6(4)9/h1-3,9H
InChI KeySSIZLKDLDKIHEV-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as o-bromophenols. These are bromophenols carrying a iodine at the C2 position of the benzene ring.
KingdomOrganic compounds
Super ClassBenzenoids
ClassPhenols
Sub ClassHalophenols
Direct ParentO-bromophenols
Alternative Parents
Substituents
  • 2-bromophenol
  • 1-hydroxy-4-unsubstituted benzenoid
  • Halobenzene
  • Bromobenzene
  • Monocyclic benzene moiety
  • Aryl halide
  • Aryl bromide
  • Organic oxygen compound
  • Hydrocarbon derivative
  • Organooxygen compound
  • Organobromide
  • Organohalogen compound
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
Biological locationRoute of exposureSource
ProcessNot Available
RoleNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point56 - 57 °CNot Available
Boiling PointNot AvailableNot Available
Water Solubility118.6 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP3.36Not Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.9 g/LALOGPS
logP3.43ALOGPS
logP3.21ChemAxon
logS-2.4ALOGPS
pKa (Strongest Acidic)6.79ChemAxon
pKa (Strongest Basic)-7.4ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area20.23 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity43.28 m³·mol⁻¹ChemAxon
Polarizability16.39 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+125.28830932474
DeepCCS[M-H]-122.48330932474
DeepCCS[M-2H]-159.08330932474
DeepCCS[M+Na]+134.05230932474
AllCCS[M+H]+146.432859911
AllCCS[M+H-H2O]+142.232859911
AllCCS[M+NH4]+150.332859911
AllCCS[M+Na]+151.432859911
AllCCS[M-H]-133.032859911
AllCCS[M+Na-2H]-135.332859911
AllCCS[M+HCOO]-137.932859911

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. 5.39 minutes32390414
Predicted by Siyang on May 30, 202215.9051 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20221.34 minutes32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid127.6 seconds40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid1885.7 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid625.5 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid243.9 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid460.7 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid332.6 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid608.0 seconds40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid704.4 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)252.1 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid1162.2 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid540.5 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid1525.1 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid578.0 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid508.4 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate718.6 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA390.5 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water222.7 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
2,6-DibromophenolOC1=C(Br)C=CC=C1Br2299.7Standard polar33892256
2,6-DibromophenolOC1=C(Br)C=CC=C1Br1292.5Standard non polar33892256
2,6-DibromophenolOC1=C(Br)C=CC=C1Br1391.3Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
2,6-Dibromophenol,1TMS,isomer #1C[Si](C)(C)OC1=C(Br)C=CC=C1Br1501.6Semi standard non polar33892256
2,6-Dibromophenol,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=C(Br)C=CC=C1Br1811.3Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 2,6-Dibromophenol GC-MS (Non-derivatized) - 70eV, Positivesplash10-0udi-0190000000-4bac4a164875d107b0892017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2,6-Dibromophenol GC-MS (1 TMS) - 70eV, Positivesplash10-00di-9164000000-5849e84c5f53ddcf88822017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2,6-Dibromophenol 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 - 2,6-Dibromophenol 10V, Positive-QTOFsplash10-0udi-0090000000-789d88d864dd8c8d5a3b2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6-Dibromophenol 20V, Positive-QTOFsplash10-0udi-0090000000-2d3833efe27f501bf96b2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6-Dibromophenol 40V, Positive-QTOFsplash10-00di-1790000000-b402044826ec4fabcfbc2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6-Dibromophenol 10V, Negative-QTOFsplash10-0002-0090000000-11b80afe2b8ab90a3d4d2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6-Dibromophenol 20V, Negative-QTOFsplash10-0002-0190000000-c6f1221e5012ba309cad2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6-Dibromophenol 40V, Negative-QTOFsplash10-014i-0920000000-17d10d52b1dac5cc32c42016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6-Dibromophenol 10V, Negative-QTOFsplash10-0002-0090000000-fdc494f356f7025d0a422021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6-Dibromophenol 20V, Negative-QTOFsplash10-0002-0090000000-fdc494f356f7025d0a422021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6-Dibromophenol 40V, Negative-QTOFsplash10-004i-9510000000-886cb655b115c5529ddf2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6-Dibromophenol 10V, Positive-QTOFsplash10-0udi-0090000000-58ecc1a9d5962101ca102021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6-Dibromophenol 20V, Positive-QTOFsplash10-0udi-0190000000-cd4722baf4fd31cf1cb92021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6-Dibromophenol 40V, Positive-QTOFsplash10-0udi-1930000000-efb37bdf0a1c4e8f07f82021-09-25Wishart 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 IDFDB008795
KNApSAcK IDC00036465
Chemspider ID11354
KEGG Compound IDC16247
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound11847
PDB IDNot Available
ChEBI ID19391
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1166251
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.. .