Record Information
Version1.0
Creation Date2016-05-27 01:45:17 UTC
Update Date2016-11-09 01:22:34 UTC
Accession NumberCHEM041929
Identification
Common Name22-oxo-docosanoate
ClassSmall Molecule
DescriptionAn oxo fatty acid anion that is the conjugate base of 22-ketodocosanoic acid, obtained by deprotonation of the carboxy group; major species at pH 7.3.
Contaminant Sources
  • FooDB Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
22-KetobehenateChEBI
22-KetodocosanoateChEBI
22-oxo-C22:0(1-)ChEBI
22-OxobehenateChEBI
Omega-ketobehenateChEBI
Omega-ketodocosanoate(1-)ChEBI
Omega-oxobehenate(1-)ChEBI
22-Ketobehenic acidGenerator
22-Ketodocosanoic acidGenerator
22-Oxobehenic acidGenerator
Omega-ketobehenic acidGenerator
Omega-ketodocosanoic acid(1-)Generator
Omega-oxobehenic acid(1-)Generator
22-Oxodocosanoic acidGenerator
Omega-oxo-docosanoateChEBI
22-oxo-Docosanoic acidGenerator
Omega-oxo-docosanoic acidGenerator
Chemical FormulaC22H41O3
Average Molecular Mass353.568 g/mol
Monoisotopic Mass353.306 g/mol
CAS Registry NumberNot Available
IUPAC Name22-oxodocosanoate
Traditional Name22-oxodocosanoate
SMILES[O-]C(=O)CCCCCCCCCCCCCCCCCCCCC=O
InChI IdentifierInChI=1S/C22H42O3/c23-21-19-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18-20-22(24)25/h21H,1-20H2,(H,24,25)/p-1
InChI KeyPYBWSGBQPKXKOQ-UHFFFAOYSA-M
Chemical Taxonomy
Description belongs to the class of organic compounds known as very long-chain fatty acids. These are fatty acids with an aliphatic tail that contains at least 22 carbon atoms.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassFatty Acyls
Sub ClassFatty acids and conjugates
Direct ParentVery long-chain fatty acids
Alternative Parents
Substituents
  • Very long-chain fatty acid
  • Straight chain fatty acid
  • Alpha-hydrogen aldehyde
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aldehyde
  • Organic anion
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
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 Solubility4.5e-05 g/LALOGPS
logP8.44ALOGPS
logP7.45ChemAxon
logS-6.9ALOGPS
pKa (Strongest Acidic)4.95ChemAxon
pKa (Strongest Basic)-6.9ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area57.2 ŲChemAxon
Rotatable Bond Count21ChemAxon
Refractivity116.27 m³·mol⁻¹ChemAxon
Polarizability46.79 ųChemAxon
Number of Rings0ChemAxon
Bioavailability0ChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0udi-0009000000-19df663d1e2a26a55db8Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0kbr-0019000000-0404040a3010985131e4Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0006-9023000000-e9ca51396e3627f4c652Spectrum
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 IDHMDB0304092
FooDB IDFDB030368
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDCPD-13098
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkNot Available
Chemspider ID30785834
ChEBI ID76298
PubChem Compound ID52940144
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available