Record Information
Version1.0
Creation Date2016-05-27 01:46:57 UTC
Update Date2016-11-09 01:22:35 UTC
Accession NumberCHEM041999
Identification
Common Name3-S-methylmercaptopropionate
ClassSmall Molecule
DescriptionA thia fatty acid anion that is the conjugate base of 3-(methylthio)propionic acid.
Contaminant Sources
  • FooDB Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
3-(Methylsulfanyl)propanoateChEBI
3-MethylthiopropanoateChEBI
3-(Methylsulfanyl)propanoic acidGenerator
3-(Methylsulphanyl)propanoateGenerator
3-(Methylsulphanyl)propanoic acidGenerator
3-Methylthiopropanoic acidGenerator
3-(Methylthio)propionic acidGenerator
3-(methylthio)PropanoateChEBI
3-(methylthio)Propanoic acidGenerator
MMPAMeSH
3-MethylmercaptopropionateMeSH
3-mercapto-2-Methylpropionic acid, monocalcium saltMeSH
3-mercapto-2-Methylpropionic acid, monopotassium saltMeSH
3-MethylthiopropionateMeSH
3-Methylthiopropionate sodium saltMeSH
3-Methylthiopropionic acidMeSH
3-mercapto-2-Methylpropionic acidMeSH
3-mercapto-2-MethylpropionateMeSH
3-mercapto-2-Methylpropionic acid, monosodium saltMeSH
3-S-Methylmercaptopropionic acidGenerator
Chemical FormulaC4H7O2S
Average Molecular Mass119.160 g/mol
Monoisotopic Mass119.017 g/mol
CAS Registry NumberNot Available
IUPAC Name3-(methylsulfanyl)propanoate
Traditional Name3-methylthiopropionate
SMILESCSCCC([O-])=O
InChI IdentifierInChI=1S/C4H8O2S/c1-7-3-2-4(5)6/h2-3H2,1H3,(H,5,6)/p-1
InChI KeyCAOMCZAIALVUPA-UHFFFAOYSA-M
Chemical Taxonomy
Description belongs to the class of organic compounds known as straight chain fatty acids. These are fatty acids with a straight aliphatic chain.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassFatty Acyls
Sub ClassFatty acids and conjugates
Direct ParentStraight chain fatty acids
Alternative Parents
Substituents
  • Straight chain fatty acid
  • Dialkylthioether
  • Sulfenyl compound
  • Thioether
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organosulfur compound
  • Organooxygen compound
  • Carbonyl group
  • 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 Solubility36.8 g/LALOGPS
logP0.37ALOGPS
logP0.83ChemAxon
logS-0.57ALOGPS
pKa (Strongest Acidic)4.68ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area40.13 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity40.56 m³·mol⁻¹ChemAxon
Polarizability11.8 ųChemAxon
Number of Rings0ChemAxon
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, Negativesplash10-01ba-9500000000-b99f06bbf801bb36c12dSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0002-9200000000-af499e35daa17287a4cfSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0002-9000000000-6f353f3ebeb29d96566cSpectrum
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 IDHMDB0304155
FooDB IDFDB030463
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkNot Available
Chemspider ID5360205
ChEBI ID49016
PubChem Compound IDNot Available
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=2505673
2. https://www.ncbi.nlm.nih.gov/pubmed/?term=3589145