Record Information
Version1.0
Creation Date2016-05-22 05:24:31 UTC
Update Date2016-11-09 01:15:50 UTC
Accession NumberCHEM018628
Identification
Common NameTetroquinone
ClassSmall Molecule
DescriptionA hydroxybenzoquinone in which all four protons of the benzoquinone structure are substituted by hydroxy groups. A systemic keratolytic, it is normally supplied as its hydrate (CHEBI:137471).
Contaminant Sources
  • ToxCast & Tox21 Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
2,3,5,6-Tetrahydroxy-2,5-cyclohexadiene-1,4-dioneChEBI
2,3,5,6-Tetrahydroxy-p-benzoquinoneChEBI
Tetrahydroxy-p-benzoquinoneChEBI
Tetrahydroxy-p-quinoneChEBI
TetrahydroxyparabenzoquinoneChEBI
TetrahydroxyquinoneChEBI
TetroquinonaChEBI
TetroquinoneChEBI
TetroquinonumChEBI
HPEK-1tetroquinoneChEMBL
Tetrahydroxy-1,4-quinoneMeSH
Chemical FormulaC6H4O6
Average Molecular Mass172.092 g/mol
Monoisotopic Mass172.001 g/mol
CAS Registry Number319-89-1
IUPAC Nametetrahydroxycyclohexa-2,5-diene-1,4-dione
Traditional Namekelox
SMILESOC1=C(O)C(=O)C(O)=C(O)C1=O
InChI IdentifierInChI=1S/C6H4O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h7-8,11-12H
InChI KeyDGQOCLATAPFASR-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as p-benzoquinones. These are benzoquinones where the two C=O groups are attached at the 1- and 4-positions, respectively.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbonyl compounds
Direct ParentP-benzoquinones
Alternative Parents
Substituents
  • P-benzoquinone
  • Vinylogous acid
  • Enediol
  • Polyol
  • Organic oxide
  • Hydrocarbon derivative
  • Aliphatic homomonocyclic compound
Molecular FrameworkAliphatic homomonocyclic compounds
External DescriptorsNot Available
Biological Properties
StatusDetected and Not Quantified
OriginNot Available
Cellular LocationsNot Available
Biofluid LocationsNot Available
Tissue LocationsNot Available
PathwaysNot Available
ApplicationsNot Available
Biological RolesNot Available
Chemical RolesNot Available
Physical Properties
StateNot Available
AppearanceNot Available
Experimental Properties
PropertyValue
Melting PointNot Available
Boiling PointNot Available
SolubilityNot Available
Predicted Properties
PropertyValueSource
Water Solubility8.49 g/LALOGPS
logP-1.3ALOGPS
logP-1.1ChemAxon
logS-1.3ALOGPS
pKa (Strongest Acidic)3.48ChemAxon
pKa (Strongest Basic)-5.9ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count6ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area115.06 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity38.9 m³·mol⁻¹ChemAxon
Polarizability13.38 ųChemAxon
Number of Rings1ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-00di-0900000000-6359412f7d8950a61433Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-00di-0900000000-990412aafc816ebbacb3Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-05fr-4900000000-92a466ad9ab567f85534Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-00di-0900000000-6c709e6549cb94de1e3cSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-00di-1900000000-6297bbb247823cf56f08Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-00e9-8900000000-9147131bf0ebecf34b09Spectrum
Toxicity Profile
Route of ExposureNot Available
Mechanism of ToxicityNot Available
MetabolismNot Available
Toxicity ValuesNot Available
Lethal DoseNot Available
Carcinogenicity (IARC Classification)Not Available
Uses/SourcesNot Available
Minimum Risk LevelNot Available
Health EffectsNot Available
SymptomsNot Available
TreatmentNot Available
Concentrations
Not Available
DrugBank IDNot Available
HMDB IDNot Available
FooDB IDNot Available
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkTetrahydroxy-1,4-benzoquinone
Chemspider IDNot Available
ChEBI ID137472
PubChem Compound ID5424
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General References
1. https://www.ncbi.nlm.nih.gov/pubmed/?term=14031813
2. https://www.ncbi.nlm.nih.gov/pubmed/?term=14095749
3. https://www.ncbi.nlm.nih.gov/pubmed/?term=16459187
4. https://www.ncbi.nlm.nih.gov/pubmed/?term=17243760
5. https://www.ncbi.nlm.nih.gov/pubmed/?term=5552869
6. https://www.ncbi.nlm.nih.gov/pubmed/?term=5572985