Record Information
Version1.0
Creation Date2016-06-03 13:19:23 UTC
Update Date2016-11-09 01:23:21 UTC
Accession NumberCHEM045471
Identification
Common Namemethyl (S)-(-)-lactate
ClassSmall Molecule
DescriptionA methyl 2-hydroxypropionate that has S configuration.
Contaminant Sources
  • STOFF IDENT Compounds
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
(-)-2-Hydroxypropanoic acid methyl esterChEBI
(-)-2-Hydroxypropionic acid methyl esterChEBI
(-)-Lactic acid methyl esterChEBI
(-)-Methyl lactateChEBI
(S)-(-)-Lactic acid methyl esterChEBI
(S)-Lactic acid methyl esterChEBI
(S)-Methyl lactateChEBI
L-Lactate methyl esterChEBI
L-Lactic acid methyl esterChEBI
L-Methyl lactateChEBI
Methyl (2S)-2-hydroxypropionateChEBI
Methyl (2S)-lactateChEBI
Methyl (S)-(-)-lactateChEBI
Methyl (S)-2-hydroxypropanoateChEBI
Methyl (S)-2-hydroxypropionateChEBI
Methyl L-lactateChEBI
(-)-2-Hydroxypropanoate methyl esterGenerator
(-)-2-Hydroxypropionate methyl esterGenerator
(-)-Lactate methyl esterGenerator
(-)-Methyl lactic acidGenerator
(S)-(-)-Lactate methyl esterGenerator
(S)-Lactate methyl esterGenerator
(S)-Methyl lactic acidGenerator
L-Methyl lactic acidGenerator
Methyl (2S)-2-hydroxypropionic acidGenerator
Methyl (2S)-lactic acidGenerator
Methyl (S)-(-)-lactic acidGenerator
Methyl (S)-2-hydroxypropanoic acidGenerator
Methyl (S)-2-hydroxypropionic acidGenerator
Methyl L-lactic acidGenerator
Methyl (S)-lactic acidGenerator
Methyl lactateMeSH
Methyl lactate, (+)-isomerMeSH
Methyl lactate, (+-)-isomerMeSH
Methyl 2-hydroxypropionateMeSH
Methyl lactate, (S)-isomerMeSH
Chemical FormulaC4H8O3
Average Molecular Mass104.105 g/mol
Monoisotopic Mass104.047 g/mol
CAS Registry Number27871-49-4
IUPAC Namemethyl (2S)-2-hydroxypropanoate
Traditional Namemethyl (2S)-2-hydroxypropanoate
SMILES[H][C@@](C)(O)C(=O)OC
InChI IdentifierInChI=1S/C4H8O3/c1-3(5)4(6)7-2/h3,5H,1-2H3/t3-/m0/s1
InChI KeyLPEKGGXMPWTOCB-VKHMYHEASA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as methyl esters. These are organic compounds containing a carboxyl group that is esterified with a methyl group. They have the general structure RC(=O)OR', where R=H or organyl group and R'=methyl group.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassCarboxylic acid derivatives
Direct ParentMethyl esters
Alternative Parents
Substituents
  • Methyl ester
  • Secondary alcohol
  • Monocarboxylic acid or derivatives
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Alcohol
  • 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 Solubility557 g/LALOGPS
logP-0.76ALOGPS
logP-0.33ChemAxon
logS0.73ALOGPS
pKa (Strongest Acidic)13ChemAxon
pKa (Strongest Basic)-3.7ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area46.53 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity23.61 m³·mol⁻¹ChemAxon
Polarizability10.1 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, Positivesplash10-0a4i-6900000000-b660934e34effa28a23eSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0abi-9300000000-58fa0aab3a72704697afSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-056s-9000000000-6f87ebe7ef9bdf46129aSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0udi-4900000000-c5f4f3c815fb1ea24f79Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0fk9-9500000000-e9b9e5bd0d9196a0f8eaSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-00dl-9000000000-518898e16bf845eacfabSpectrum
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 IDNot Available
FooDB IDNot Available
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkNot Available
Chemspider IDNot Available
ChEBI ID83222
PubChem Compound ID94386
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=10835235