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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 01:07:11 UTC
Update Date2022-03-07 02:56:16 UTC
HMDB IDHMDB0039614
Secondary Accession Numbers
  • HMDB39614
Metabolite Identification
Common Name3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl
Description3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl belongs to the class of organic compounds known as biphenols. These are organic compounds containing two phenol groups linked together by a C-C bond. 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl has been detected, but not quantified in, herbs and spices. This could make 3,4,4'-trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl.
Structure
Data?1563863408
SynonymsNot Available
Chemical FormulaC20H26O3
Average Molecular Weight314.4186
Monoisotopic Molecular Weight314.188194698
IUPAC Name4-[4-hydroxy-2-methyl-5-(propan-2-yl)phenyl]-3-methyl-6-(propan-2-yl)benzene-1,2-diol
Traditional Name4-(4-hydroxy-5-isopropyl-2-methylphenyl)-6-isopropyl-3-methylbenzene-1,2-diol
CAS Registry Number123132-69-4
SMILES
CC(C)C1=CC(=C(C)C(O)=C1O)C1=CC(C(C)C)=C(O)C=C1C
InChI Identifier
InChI=1S/C20H26O3/c1-10(2)14-8-16(12(5)7-18(14)21)17-9-15(11(3)4)20(23)19(22)13(17)6/h7-11,21-23H,1-6H3
InChI KeyHNHWYZDOESMBLD-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as biphenols. These are organic compounds containing two phenol groups linked together by a C-C bond.
KingdomOrganic compounds
Super ClassBenzenoids
ClassBenzene and substituted derivatives
Sub ClassBiphenols
Direct ParentBiphenols
Alternative Parents
Substituents
  • Biphenol
  • Biphenyl
  • P-cymene
  • Aromatic monoterpenoid
  • Monocyclic monoterpenoid
  • Monoterpenoid
  • Cumene
  • Phenylpropane
  • O-cresol
  • M-cresol
  • Catechol
  • Phenol
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Toluene
  • Organooxygen compound
  • Hydrocarbon derivative
  • Organic oxygen compound
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point75 °CNot Available
Boiling PointNot AvailableNot Available
Water Solubility0.15 mg/L @ 25 °C (est)The Good Scents Company Information System
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.0083 g/LALOGPS
logP4.37ALOGPS
logP6.23ChemAxon
logS-4.6ALOGPS
pKa (Strongest Acidic)9.69ChemAxon
pKa (Strongest Basic)-5.2ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area60.69 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity95.6 m³·mol⁻¹ChemAxon
Polarizability36.52 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+176.36131661259
DarkChem[M-H]-175.08331661259
DeepCCS[M+H]+182.34130932474
DeepCCS[M-H]-179.98330932474
DeepCCS[M-2H]-214.01430932474
DeepCCS[M+Na]+189.24230932474
AllCCS[M+H]+174.332859911
AllCCS[M+H-H2O]+171.032859911
AllCCS[M+NH4]+177.332859911
AllCCS[M+Na]+178.232859911
AllCCS[M-H]-184.432859911
AllCCS[M+Na-2H]-184.332859911
AllCCS[M+HCOO]-184.332859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenylCC(C)C1=CC(=C(C)C(O)=C1O)C1=CC(C(C)C)=C(O)C=C1C3745.8Standard polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenylCC(C)C1=CC(=C(C)C(O)=C1O)C1=CC(C(C)C)=C(O)C=C1C2486.0Standard non polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenylCC(C)C1=CC(=C(C)C(O)=C1O)C1=CC(C(C)C)=C(O)C=C1C2557.9Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl,1TMS,isomer #1CC1=CC(O)=C(C(C)C)C=C1C1=CC(C(C)C)=C(O)C(O[Si](C)(C)C)=C1C2530.3Semi standard non polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl,1TMS,isomer #2CC1=CC(O)=C(C(C)C)C=C1C1=CC(C(C)C)=C(O[Si](C)(C)C)C(O)=C1C2515.6Semi standard non polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl,1TMS,isomer #3CC1=CC(O[Si](C)(C)C)=C(C(C)C)C=C1C1=CC(C(C)C)=C(O)C(O)=C1C2539.5Semi standard non polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl,2TMS,isomer #1CC1=CC(O[Si](C)(C)C)=C(C(C)C)C=C1C1=CC(C(C)C)=C(O)C(O[Si](C)(C)C)=C1C2440.2Semi standard non polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl,2TMS,isomer #2CC1=CC(O)=C(C(C)C)C=C1C1=CC(C(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C2495.9Semi standard non polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl,2TMS,isomer #3CC1=CC(O[Si](C)(C)C)=C(C(C)C)C=C1C1=CC(C(C)C)=C(O[Si](C)(C)C)C(O)=C1C2453.1Semi standard non polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl,3TMS,isomer #1CC1=CC(O[Si](C)(C)C)=C(C(C)C)C=C1C1=CC(C(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C2467.5Semi standard non polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl,1TBDMS,isomer #1CC1=CC(O)=C(C(C)C)C=C1C1=CC(C(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1C2809.3Semi standard non polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl,1TBDMS,isomer #2CC1=CC(O)=C(C(C)C)C=C1C1=CC(C(C)C)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1C2799.5Semi standard non polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl,1TBDMS,isomer #3CC1=CC(O[Si](C)(C)C(C)(C)C)=C(C(C)C)C=C1C1=CC(C(C)C)=C(O)C(O)=C1C2827.4Semi standard non polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl,2TBDMS,isomer #1CC1=CC(O[Si](C)(C)C(C)(C)C)=C(C(C)C)C=C1C1=CC(C(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1C2962.0Semi standard non polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl,2TBDMS,isomer #2CC1=CC(O)=C(C(C)C)C=C1C1=CC(C(C)C)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1C2981.4Semi standard non polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl,2TBDMS,isomer #3CC1=CC(O[Si](C)(C)C(C)(C)C)=C(C(C)C)C=C1C1=CC(C(C)C)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1C2972.5Semi standard non polar33892256
3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl,3TBDMS,isomer #1CC1=CC(O[Si](C)(C)C(C)(C)C)=C(C(C)C)C=C1C1=CC(C(C)C)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1C3162.0Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl GC-MS (Non-derivatized) - 70eV, Positivesplash10-0002-0091000000-136e41e0e72161a138e52017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl GC-MS (3 TMS) - 70eV, Positivesplash10-014i-0000390000-29864c3f68eca525e5df2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl 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 - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl 10V, Positive-QTOFsplash10-014i-0129000000-cd5cef46d50788c215a52016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl 20V, Positive-QTOFsplash10-01b9-1293000000-f929736992bd7323ae0d2016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl 40V, Positive-QTOFsplash10-00ks-1790000000-568ff756eee668c814c62016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl 10V, Negative-QTOFsplash10-03di-0009000000-8a79dfddc504d77f9bdd2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl 20V, Negative-QTOFsplash10-03di-0049000000-d2cd3f363f78a359637a2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl 40V, Negative-QTOFsplash10-059t-0190000000-c1e8846a31269ca534692016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl 10V, Positive-QTOFsplash10-014i-0059000000-89bfbb2f9f70e072493e2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl 20V, Positive-QTOFsplash10-0300-0098000000-eb967d120e800a9f60422021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl 40V, Positive-QTOFsplash10-00kr-0950000000-12bbd60f6a0545625a3c2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl 10V, Negative-QTOFsplash10-03di-0009000000-d8638daf32922c2274642021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl 20V, Negative-QTOFsplash10-03di-0059000000-f39903f3b7ef21e00bbf2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,4,4'-Trihydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl 40V, Negative-QTOFsplash10-00b9-0290000000-8f4c85a492f011c740fa2021-09-24Wishart 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 IDFDB019242
KNApSAcK IDC00057828
Chemspider ID10276704
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound14396469
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1878821
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.. .