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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 19:05:09 UTC
Update Date2022-03-07 02:54:03 UTC
HMDB IDHMDB0034281
Secondary Accession Numbers
  • HMDB34281
Metabolite Identification
Common NameEgonol gentiobioside
DescriptionEgonol gentiobioside belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. Egonol gentiobioside has been detected, but not quantified in, a few different foods, such as common mushrooms (Agaricus bisporus), mushrooms, and oyster mushrooms (Pleurotus ostreatus). This could make egonol gentiobioside a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Egonol gentiobioside.
Structure
Data?1563862539
Synonyms
ValueSource
Egonol gentiobiosideMeSH
Chemical FormulaC31H38O15
Average Molecular Weight650.6244
Monoisotopic Molecular Weight650.221070546
IUPAC Name2-{3-[2-(2H-1,3-benzodioxol-5-yl)-7-methoxy-1-benzofuran-5-yl]propoxy}-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxane-3,4,5-triol
Traditional Name2-{3-[2-(2H-1,3-benzodioxol-5-yl)-7-methoxy-1-benzofuran-5-yl]propoxy}-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxane-3,4,5-triol
CAS Registry NumberNot Available
SMILES
COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O)C(O)C2O)=CC2=C1OC(=C2)C1=CC2=C(OCO2)C=C1
InChI Identifier
InChI=1S/C31H38O15/c1-39-20-8-14(7-16-10-18(44-29(16)20)15-4-5-17-19(9-15)43-13-42-17)3-2-6-40-30-27(37)26(36)24(34)22(46-30)12-41-31-28(38)25(35)23(33)21(11-32)45-31/h4-5,7-10,21-28,30-38H,2-3,6,11-13H2,1H3
InChI KeyNBGJGWFIDMDCAW-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
Class2-arylbenzofuran flavonoids
Sub ClassNot Available
Direct Parent2-arylbenzofuran flavonoids
Alternative Parents
Substituents
  • 2-arylbenzofuran flavonoid
  • Lignan glycoside
  • Neolignan skeleton
  • Fatty acyl glycoside
  • Fatty acyl glycoside of mono- or disaccharide
  • Alkyl glycoside
  • Disaccharide
  • Glycosyl compound
  • O-glycosyl compound
  • Benzodioxole
  • Benzofuran
  • Anisole
  • Alkyl aryl ether
  • Oxane
  • Fatty acyl
  • Benzenoid
  • Heteroaromatic compound
  • Furan
  • Secondary alcohol
  • Polyol
  • Oxacycle
  • Acetal
  • Ether
  • Organoheterocyclic compound
  • Organic oxygen compound
  • Alcohol
  • Hydrocarbon derivative
  • Primary alcohol
  • Organooxygen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point147 - 149 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.95 g/LALOGPS
logP0.35ALOGPS
logP-0.41ChemAxon
logS-2.8ALOGPS
pKa (Strongest Acidic)11.91ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count14ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area219.36 ŲChemAxon
Rotatable Bond Count11ChemAxon
Refractivity153.14 m³·mol⁻¹ChemAxon
Polarizability67.67 ųChemAxon
Number of Rings6ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+246.7631661259
DarkChem[M-H]-241.5831661259
DeepCCS[M+H]+238.24930932474
DeepCCS[M-H]-236.28430932474
DeepCCS[M-2H]-269.52430932474
DeepCCS[M+Na]+244.38930932474
AllCCS[M+H]+242.432859911
AllCCS[M+H-H2O]+241.632859911
AllCCS[M+NH4]+243.232859911
AllCCS[M+Na]+243.432859911
AllCCS[M-H]-233.332859911
AllCCS[M+Na-2H]-236.632859911
AllCCS[M+HCOO]-240.332859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Egonol gentiobiosideCOC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O)C(O)C2O)=CC2=C1OC(=C2)C1=CC2=C(OCO2)C=C14910.6Standard polar33892256
Egonol gentiobiosideCOC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O)C(O)C2O)=CC2=C1OC(=C2)C1=CC2=C(OCO2)C=C15206.7Standard non polar33892256
Egonol gentiobiosideCOC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O)C(O)C2O)=CC2=C1OC(=C2)C1=CC2=C(OCO2)C=C15840.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Egonol gentiobioside,1TMS,isomer #1COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25531.7Semi standard non polar33892256
Egonol gentiobioside,1TMS,isomer #2COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25502.8Semi standard non polar33892256
Egonol gentiobioside,1TMS,isomer #3COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25477.6Semi standard non polar33892256
Egonol gentiobioside,1TMS,isomer #4COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25477.6Semi standard non polar33892256
Egonol gentiobioside,1TMS,isomer #5COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25521.9Semi standard non polar33892256
Egonol gentiobioside,1TMS,isomer #6COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25502.8Semi standard non polar33892256
Egonol gentiobioside,1TMS,isomer #7COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25500.7Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #1COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25457.0Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #10COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25383.3Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #11COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25395.8Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #12COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25392.9Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #13COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25382.8Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #14COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25342.7Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #15COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25355.1Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #16COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25399.2Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #17COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25353.3Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #18COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25376.9Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #19COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25415.4Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #2COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25416.6Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #20COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25437.0Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #21COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25416.0Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #3COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25434.5Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #4COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25456.9Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #5COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25415.1Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #6COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25433.4Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #7COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25385.4Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #8COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25387.7Semi standard non polar33892256
Egonol gentiobioside,2TMS,isomer #9COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25422.2Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #1COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25298.1Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #10COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25321.7Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #11COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25256.5Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #12COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25305.9Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #13COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25296.4Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #14COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25336.6Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #15COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25305.0Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #16COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25293.7Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #17COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25272.4Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #18COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25218.0Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #19COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25255.1Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #2COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25330.7Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #20COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25288.8Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #21COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25231.5Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #22COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25273.1Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #23COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25285.2Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #24COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25320.6Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #25COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25291.2Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #26COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25281.6Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #27COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25227.7Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #28COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25264.7Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #29COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25233.5Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #3COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25336.6Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #30COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25260.5Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #31COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25236.6Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #32COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25259.9Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #33COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25294.5Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #34COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25266.8Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #35COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25359.5Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #4COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25273.9Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #5COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25318.6Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #6COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25304.7Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #7COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25277.5Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #8COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25222.2Semi standard non polar33892256
Egonol gentiobioside,3TMS,isomer #9COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25258.1Semi standard non polar33892256
Egonol gentiobioside,1TBDMS,isomer #1COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25765.9Semi standard non polar33892256
Egonol gentiobioside,1TBDMS,isomer #2COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25761.1Semi standard non polar33892256
Egonol gentiobioside,1TBDMS,isomer #3COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25734.2Semi standard non polar33892256
Egonol gentiobioside,1TBDMS,isomer #4COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25726.5Semi standard non polar33892256
Egonol gentiobioside,1TBDMS,isomer #5COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25773.2Semi standard non polar33892256
Egonol gentiobioside,1TBDMS,isomer #6COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25756.0Semi standard non polar33892256
Egonol gentiobioside,1TBDMS,isomer #7COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25749.6Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #1COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25870.8Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #10COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25843.1Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #11COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25840.9Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #12COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25845.6Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #13COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25834.9Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #14COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25803.9Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #15COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25797.1Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #16COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25831.1Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #17COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25797.2Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #18COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25802.3Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #19COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25877.6Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #2COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25839.2Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #20COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25889.8Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #21COC1=CC(CCCOC2OC(COC3OC(CO)C(O)C(O)C3O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25877.6Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #3COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25849.6Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #4COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25870.4Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #5COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25837.0Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #6COC1=CC(CCCOC2OC(COC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25843.2Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #7COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25833.2Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #8COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25834.2Semi standard non polar33892256
Egonol gentiobioside,2TBDMS,isomer #9COC1=CC(CCCOC2OC(COC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC2=C1OC(C1=CC=C3OCOC3=C1)=C25870.8Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (Non-derivatized) - 70eV, Positivesplash10-001r-5753239000-7c6834a0fefa949f99e72017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_15) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_16) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Egonol gentiobioside GC-MS (TMS_2_17) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Egonol gentiobioside 10V, Positive-QTOFsplash10-0f89-0103109000-94a2ed2cb88f1db52bbf2016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Egonol gentiobioside 20V, Positive-QTOFsplash10-0a6r-1209201000-f62f1593355ef3b344992016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Egonol gentiobioside 40V, Positive-QTOFsplash10-0bvj-5918233000-47e9242788d95e64a8c72016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Egonol gentiobioside 10V, Negative-QTOFsplash10-002b-3525209000-0763443ad6579bbb35c22016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Egonol gentiobioside 20V, Negative-QTOFsplash10-020r-4915005000-aa1483381e3d7a3bcbc92016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Egonol gentiobioside 40V, Negative-QTOFsplash10-056u-9413010000-3d998373e17367bdfb502016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Egonol gentiobioside 10V, Positive-QTOFsplash10-004i-0009203000-d8641fee5acff6ae34e12021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Egonol gentiobioside 20V, Positive-QTOFsplash10-0aos-1539313000-ae96969b236260b621872021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Egonol gentiobioside 40V, Positive-QTOFsplash10-0bt9-0169100000-56e1d90bf33eb765323c2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Egonol gentiobioside 10V, Negative-QTOFsplash10-0002-0001009000-edf42f6147ade35d77042021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Egonol gentiobioside 20V, Negative-QTOFsplash10-054t-4217249000-a85c5b313f7e36455ee22021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Egonol gentiobioside 40V, Negative-QTOFsplash10-052r-9021433000-fb9fa37910bcb22a3ead2021-09-23Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Extracellular
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 IDFDB012618
KNApSAcK IDC00032932
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound74960882
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
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.. .