Record Information
Version1.0
Creation Date2016-06-03 10:11:56 UTC
Update Date2016-11-09 01:22:48 UTC
Accession NumberCHEM042790
Identification
Common Name1-butan-sulfonic acid
ClassSmall Molecule
DescriptionAn alkanesulfonic acid in which the alkyl group directly linked to the sulfo functionality is butyl.
Contaminant Sources
  • STOFF IDENT Compounds
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
1-Butanesulfonic acidChEBI
Butane sulfonic acidChEBI
Butane-1-sulphonic acidChEBI
Butanesulfonic acidChEBI
N-Butane sulfonic acidChEBI
N-Butane-1-sulfonic acidChEBI
N-Butanesulphonic acidChEBI
1-ButanesulfonateGenerator
1-ButanesulphonateGenerator
1-Butanesulphonic acidGenerator
Butane sulfonateGenerator
Butane sulphonateGenerator
Butane sulphonic acidGenerator
Butane-1-sulfonateGenerator
Butane-1-sulphonateGenerator
ButanesulfonateGenerator
ButanesulphonateGenerator
Butanesulphonic acidGenerator
N-Butane sulfonateGenerator
N-Butane sulphonateGenerator
N-Butane sulphonic acidGenerator
N-Butane-1-sulfonateGenerator
N-Butane-1-sulphonateGenerator
N-Butane-1-sulphonic acidGenerator
N-ButanesulfonateGenerator
N-Butanesulfonic acidGenerator
N-ButanesulphonateGenerator
1-Butanesulfonic acid sodium saltMeSH
Chemical FormulaC4H10O3S
Average Molecular Mass138.180 g/mol
Monoisotopic Mass138.035 g/mol
CAS Registry Number2386-47-2
IUPAC Namebutane-1-sulfonic acid
Traditional Namebutanesulfonic acid
SMILESCCCCS(O)(=O)=O
InChI IdentifierInChI=1S/C4H10O3S/c1-2-3-4-8(5,6)7/h2-4H2,1H3,(H,5,6,7)
InChI KeyQDHFHIQKOVNCNC-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as organosulfonic acids. Organosulfonic acids are compounds containing the sulfonic acid group, which has the general structure RS(=O)2OH (R is not a hydrogen atom).
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassOrganic sulfonic acids and derivatives
Sub ClassOrganosulfonic acids and derivatives
Direct ParentOrganosulfonic acids
Alternative Parents
Substituents
  • Alkanesulfonic acid
  • Sulfonyl
  • Organosulfonic acid
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organosulfur compound
  • 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 Solubility18.7 g/LALOGPS
logP-1ALOGPS
logP0.52ChemAxon
logS-0.87ALOGPS
pKa (Strongest Acidic)-0.87ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area54.37 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity30.53 m³·mol⁻¹ChemAxon
Polarizability13.45 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, Positivesplash10-000i-0900000000-6de7996ae837ff39aae4Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0a4i-9300000000-6ab9565897f6287c011bSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0a4l-9000000000-3eb706035df068e67f8eSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-000i-4900000000-df6c1c081e457fba55e8Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-001r-9300000000-6b0d881aad19ec0a5363Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-001i-9000000000-1682b311502b1693c9b5Spectrum
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 ID61958
PubChem Compound ID49935
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available