Record Information
Version1.0
Creation Date2016-09-30 22:49:38 UTC
Update Date2020-05-05 18:37:53 UTC
BMDB IDBMDB0001988
Secondary Accession Numbers
  • BMDB01988
Metabolite Identification
Common Name4-Hydroxycyclohexylcarboxylic acid
Description4-Hydroxycyclohexylcarboxylic acid belongs to the class of organic compounds known as cyclohexanols. Cyclohexanols are compounds containing an alcohol group attached to a cyclohexane ring. Based on a literature review a significant number of articles have been published on 4-Hydroxycyclohexylcarboxylic acid.
Structure
Thumb
Synonyms
ValueSource
4-HydroxycyclohexylcarboxylateGenerator
4-Hydroxycyclohexane-1-carboxylic acidHMDB
4-Hydroxycyclohexanecarboxylic acidHMDB, MeSH
4-HCHCMeSH, HMDB
4-Hydroxycyclohexane-1-carboxylateGenerator, HMDB
Chemical FormulaC7H12O3
Average Molecular Weight144.1684
Monoisotopic Molecular Weight144.07864425
IUPAC Name4-hydroxycyclohexane-1-carboxylic acid
Traditional Name4-hydroxycyclohexane-1-carboxylic acid
CAS Registry Number17419-81-7
SMILES
OC1CCC(CC1)C(O)=O
InChI Identifier
InChI=1S/C7H12O3/c8-6-3-1-5(2-4-6)7(9)10/h5-6,8H,1-4H2,(H,9,10)
InChI KeyHCFRWBBJISAZNK-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as cyclohexanols. Cyclohexanols are compounds containing an alcohol group attached to a cyclohexane ring.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassAlcohols and polyols
Direct ParentCyclohexanols
Alternative Parents
Substituents
  • Cyclohexanol
  • Cyclic alcohol
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Organic oxide
  • Hydrocarbon derivative
  • Carbonyl group
  • Aliphatic homomonocyclic compound
Molecular FrameworkAliphatic homomonocyclic compounds
External DescriptorsNot Available
Ontology
StatusDetected but not Quantified
Origin
  • Endogenous
  • Exogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locationsNot Available
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP0.56ALOGPS
logP0.5ChemAxon
logS0.03ALOGPS
pKa (Strongest Acidic)4.51ChemAxon
pKa (Strongest Basic)-1.4ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area57.53 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity35.52 m³·mol⁻¹ChemAxon
Polarizability14.94 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash Key
GC-MSGC-MS Spectrum - GC-EI-TOF (Non-derivatized)splash10-00ea-0930000000-847fab622854d8969240View in MoNA
GC-MSGC-MS Spectrum - GC-EI-TOF (Non-derivatized)splash10-00ea-0930000000-847fab622854d8969240View in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positivesplash10-004v-9100000000-4c1f052d143e49157a80View in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (2 TMS) - 70eV, Positivesplash10-00di-5930000000-0d79b67d3319b73f908fView in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, PositiveNot AvailableView in JSpectraViewer
LC-MS/MSLC-MS/MS Spectrum - Quattro_QQQ 10V, Positive (Annotated)splash10-057i-3900000000-abc6ac16f21e5ce06844View in MoNA
LC-MS/MSLC-MS/MS Spectrum - Quattro_QQQ 25V, Positive (Annotated)splash10-001i-9000000000-88770293822bd2e9b1d9View in MoNA
LC-MS/MSLC-MS/MS Spectrum - Quattro_QQQ 40V, Positive (Annotated)splash10-0059-9000000000-35f3ef9952979b17e396View in MoNA
LC-MS/MSLC-MS/MS Spectrum - 40V, Negativesplash10-0005-9000000000-1b2cea72343cecc8e91bView in MoNA
LC-MS/MSLC-MS/MS Spectrum - 10V, Negativesplash10-0006-0900000000-96b59c40cd0d646bd69fView in MoNA
LC-MS/MSLC-MS/MS Spectrum - 20V, Negativesplash10-0007-8900000000-057e4d949aac31b31260View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-004j-2900000000-8fe3526038b3ae3e8c9dView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-057j-7900000000-8e6b4bce93588dedbed0View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-05o0-9000000000-1ed081d3979985a45ba0View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0006-3900000000-59651bf351fcc5fcf4bbView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0035-9700000000-6e8062fddb5dc431fcd1View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-000t-9100000000-1800082b5d54d2e7dc91View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0006-2900000000-9c4062159f99a6e08237View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-001m-9200000000-d66d5f669e271d14dedeView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0006-9000000000-b48b8d0bf36e587fd68eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-000t-9500000000-795337373081b3c6fe8fView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-053s-9200000000-ff4f103a5daa54c21114View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0pbc-9000000000-ac84b42ef25ecdf00179View in MoNA
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Liver
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
LiverDetected but not QuantifiedNot QuantifiedNot SpecifiedNot Specified
Normal
details
LiverDetected but not QuantifiedNot QuantifiedNot SpecifiedNot Specified
Normal
details
Abnormal Concentrations
Not Available
HMDB IDHMDB0001988
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB022785
KNApSAcK IDNot Available
Chemspider ID133210
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound151138
PDB IDNot Available
ChEBI ID16817
References
Synthesis ReferenceInoue, Goro; Kato, Toshio; Oshima, Noboru. 4-Hydroxycyclohexanecarboxylic acid and its related compounds. Jpn. Tokkyo Koho (1968), 3 pp.
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available