Hmdb loader
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2013-07-04 18:54:36 UTC
Update Date2023-02-21 17:30:11 UTC
HMDB IDHMDB0060715
Secondary Accession Numbers
  • HMDB60715
Metabolite Identification
Common Name2-Hydroxy-4-trifluoromethyl benzoic acid
Description2-Hydroxy-4-trifluoromethyl benzoic acid is a metabolite of triflusal. Triflusal is a platelet aggregation inhibitor that was discovered and developed in the Uriach Laboratories, and commercialised in Spain since 1981. Currently, it is available in 25 countries in Europe, Asia, Africa and America. It is a drug of the salicylate family but it is not a derivative of acetylsalicylic acid (ASA). Trade names include Disgren, Grendis, Aflen and Triflux (Wikipedia)
Structure
Data?1677000611
Synonyms
ValueSource
2-Hydroxy-4-trifluoromethyl benzoateGenerator
2-Hydroxy-4-trifluoromethylbenzoic acidHMDB
4-TFMSAHMDB
HTBHMDB
4-Trifluoromethylsalicylic acidMeSH
Chemical FormulaC8H5F3O3
Average Molecular Weight206.1187
Monoisotopic Molecular Weight206.019078641
IUPAC Name2-hydroxy-4-(trifluoromethyl)benzoic acid
Traditional Name2-hydroxy-4-(trifluoromethyl)benzoic acid
CAS Registry Number328-90-5
SMILES
OC(=O)C1=C(O)C=C(C=C1)C(F)(F)F
InChI Identifier
InChI=1S/C8H5F3O3/c9-8(10,11)4-1-2-5(7(13)14)6(12)3-4/h1-3,12H,(H,13,14)
InChI KeyXMLFPUBZFSJWCN-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as salicylic acids. These are ortho-hydroxylated benzoic acids.
KingdomOrganic compounds
Super ClassBenzenoids
ClassBenzene and substituted derivatives
Sub ClassBenzoic acids and derivatives
Direct ParentSalicylic acids
Alternative Parents
Substituents
  • Trifluoromethylbenzene
  • Salicylic acid
  • Benzoic acid
  • Benzoyl
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Phenol
  • Vinylogous acid
  • Carboxylic acid derivative
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Alkyl fluoride
  • Organohalogen compound
  • Organofluoride
  • Organooxygen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organic oxygen compound
  • Alkyl halide
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility3.19 g/LALOGPS
logP2.79ALOGPS
logP2.86ChemAxon
logS-1.8ALOGPS
pKa (Strongest Acidic)2.76ChemAxon
pKa (Strongest Basic)-6.3ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area57.53 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity41.27 m³·mol⁻¹ChemAxon
Polarizability15.32 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+145.08330932474
DeepCCS[M-H]-142.68730932474
DeepCCS[M-2H]-176.82830932474
DeepCCS[M+Na]+151.26430932474
AllCCS[M+H]+141.732859911
AllCCS[M+H-H2O]+137.632859911
AllCCS[M+NH4]+145.632859911
AllCCS[M+Na]+146.732859911
AllCCS[M-H]-133.632859911
AllCCS[M+Na-2H]-133.932859911
AllCCS[M+HCOO]-134.432859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
2-Hydroxy-4-trifluoromethyl benzoic acidOC(=O)C1=C(O)C=C(C=C1)C(F)(F)F1950.4Standard polar33892256
2-Hydroxy-4-trifluoromethyl benzoic acidOC(=O)C1=C(O)C=C(C=C1)C(F)(F)F1284.6Standard non polar33892256
2-Hydroxy-4-trifluoromethyl benzoic acidOC(=O)C1=C(O)C=C(C=C1)C(F)(F)F1342.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
2-Hydroxy-4-trifluoromethyl benzoic acid,1TMS,isomer #1C[Si](C)(C)OC(=O)C1=CC=C(C(F)(F)F)C=C1O1320.9Semi standard non polar33892256
2-Hydroxy-4-trifluoromethyl benzoic acid,1TMS,isomer #2C[Si](C)(C)OC1=CC(C(F)(F)F)=CC=C1C(=O)O1411.8Semi standard non polar33892256
2-Hydroxy-4-trifluoromethyl benzoic acid,2TMS,isomer #1C[Si](C)(C)OC(=O)C1=CC=C(C(F)(F)F)C=C1O[Si](C)(C)C1435.2Semi standard non polar33892256
2-Hydroxy-4-trifluoromethyl benzoic acid,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)C1=CC=C(C(F)(F)F)C=C1O1560.5Semi standard non polar33892256
2-Hydroxy-4-trifluoromethyl benzoic acid,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC(C(F)(F)F)=CC=C1C(=O)O1638.7Semi standard non polar33892256
2-Hydroxy-4-trifluoromethyl benzoic acid,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)C1=CC=C(C(F)(F)F)C=C1O[Si](C)(C)C(C)(C)C1869.0Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-trifluoromethyl benzoic acid GC-MS (Non-derivatized) - 70eV, Positivesplash10-052r-1920000000-c2e6f654f7493ecf208d2017-09-20Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-trifluoromethyl benzoic acid GC-MS (2 TMS) - 70eV, Positivesplash10-03ki-7093000000-11fc1ca514c8731fb0d72017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-trifluoromethyl benzoic acid 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-Hydroxy-4-trifluoromethyl benzoic acid 10V, Positive-QTOFsplash10-0a4i-0490000000-71e7e000d95d3059ed672016-08-02Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-trifluoromethyl benzoic acid 20V, Positive-QTOFsplash10-052r-0940000000-18198ce85355627778b22016-08-02Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-trifluoromethyl benzoic acid 40V, Positive-QTOFsplash10-029j-3900000000-99375180a53bb58704712016-08-02Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-trifluoromethyl benzoic acid 10V, Negative-QTOFsplash10-0bt9-0690000000-2cc450bf3a04d68c71832016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-trifluoromethyl benzoic acid 20V, Negative-QTOFsplash10-03di-0910000000-6b25e242e4423c7d86f12016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-trifluoromethyl benzoic acid 40V, Negative-QTOFsplash10-03di-3900000000-084bfb083d8f242ac65f2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-trifluoromethyl benzoic acid 10V, Negative-QTOFsplash10-0bt9-0490000000-61c8d41358625c8327a92021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-trifluoromethyl benzoic acid 20V, Negative-QTOFsplash10-03di-0930000000-5371c30a8d1fd3bff4032021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-trifluoromethyl benzoic acid 40V, Negative-QTOFsplash10-03xr-4900000000-c6ce02cdf694fde921122021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-trifluoromethyl benzoic acid 10V, Positive-QTOFsplash10-000i-0920000000-9c142b14a4e679a2022b2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-trifluoromethyl benzoic acid 20V, Positive-QTOFsplash10-000i-0900000000-e91bfa454898f0ba31ff2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-trifluoromethyl benzoic acid 40V, Positive-QTOFsplash10-014i-9400000000-b7402802a84cf1401d932021-10-12Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum

IR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M-H]-)2023-02-04FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)2023-02-04FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)2023-02-04FELIX labView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Membrane (predicted from logP)
Biospecimen Locations
  • Blood
  • Urine
Tissue Locations
  • Kidney
  • Liver
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodExpected but not QuantifiedNot QuantifiedNot AvailableNot AvailableNormal
      Not Available
details
UrineExpected but not QuantifiedNot QuantifiedNot AvailableNot AvailableNormal
      Not Available
details
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound164578
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 ReferencesNot Available