Record Information
Version1.0
Creation Date2016-05-19 01:56:40 UTC
Update Date2016-11-09 01:09:27 UTC
Accession NumberCHEM004956
Identification
Common NameCALCIUM LAURATE
ClassSmall Molecule
DescriptionNot Available
Contaminant Sources
  • EAFUS Chemicals
  • FooDB Chemicals
  • HPV EPA Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
Calcium lauric acidGenerator
Dodecanoic acidMeSH
Lauric acid, lithium saltMeSH
Lauric acid, nickel(2+) saltMeSH
Sodium dodecanoateMeSH
Lauric acid, barium and cadmium salt (4:1:1)MeSH
Lauric acid, calcium saltMeSH
Lauric acid, potassium saltMeSH
Sodium laurateMeSH
Lauric acid, ammonium saltMeSH
Lauric acid, magnesium saltMeSH
Lauric acid, sodium saltMeSH
Potassium laurateMeSH
Lauric acidMeSH
Calcium dodecanoic acidGenerator
Chemical FormulaC24H46CaO4
Average Molecular Mass438.698 g/mol
Monoisotopic Mass438.302 g/mol
CAS Registry Number4696-56-4
IUPAC Namecalcium didodecanoate
Traditional Namecalcium dilaurate
SMILES[Ca++].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O
InChI IdentifierInChI=1S/2C12H24O2.Ca/c2*1-2-3-4-5-6-7-8-9-10-11-12(13)14;/h2*2-11H2,1H3,(H,13,14);/q;;+2/p-2
InChI KeyHIAAVKYLDRCDFQ-UHFFFAOYSA-L
Chemical Taxonomy
Description belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassFatty Acyls
Sub ClassFatty acids and conjugates
Direct ParentMedium-chain fatty acids
Alternative Parents
Substituents
  • Medium-chain fatty acid
  • Straight chain fatty acid
  • Carboxylic acid salt
  • Organic calcium salt
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organic salt
  • Organooxygen compound
  • Carbonyl group
  • Aliphatic acyclic compound
Molecular FrameworkNot Available
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 Solubility2.6e-05 g/LALOGPS
logP9.07ALOGPS
logP4.48ChemAxon
logS-7.2ALOGPS
pKa (Strongest Acidic)4.95ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area40.13 ŲChemAxon
Rotatable Bond Count20ChemAxon
Refractivity69.52 m³·mol⁻¹ChemAxon
Polarizability25.37 ųChemAxon
Number of Rings0ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
SpectraNot Available
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 IDHMDB0303348
FooDB IDFDB011454
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkNot Available
Chemspider ID8086691
ChEBI IDNot Available
PubChem Compound ID9911040
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available