Record Information
Version1.0
Creation Date2016-05-22 04:29:58 UTC
Update Date2016-11-09 01:15:38 UTC
Accession NumberCHEM017620
Identification
Common NameChloramine-T trihydrate
ClassSmall Molecule
Description
Contaminant Sources
  • ToxCast & Tox21 Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
Chloramine-T trihydric acidGenerator
HydroclonazoneMeSH
Chloramine-TMeSH
Chloramine-T anhydrousMeSH
Sodium p-toluenesulfonchloramideMeSH
Chloramine TMeSH
ClorinaMeSH
EuclorinaMeSH
(N-Chloro-p-toluenesulfonamide)sodiumMeSH
Chloramine-T, 36CL-labeledMeSH
Sodium chloro(4-methylbenzenesulfonyl)azanide trihydric acidGenerator
Sodium chloro(4-methylbenzenesulphonyl)azanide trihydrateGenerator
Sodium chloro(4-methylbenzenesulphonyl)azanide trihydric acidGenerator
Chemical FormulaC7H13ClNNaO5S
Average Molecular Mass281.680 g/mol
Monoisotopic Mass281.010 g/mol
CAS Registry Number7080-50-4
IUPAC Namesodium chloro(4-methylbenzenesulfonyl)azanide trihydrate
Traditional Namesodium chloramine T anion trihydrate
SMILESO.O.O.[Na+].CC1=CC=C(C=C1)S(=O)(=O)[N-]Cl
InChI IdentifierInChI=1S/C7H7ClNO2S.Na.3H2O/c1-6-2-4-7(5-3-6)12(10,11)9-8;;;;/h2-5H,1H3;;3*1H2/q-1;+1;;;
InChI KeyNZYOAGBNMCVQIV-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as benzenesulfonamides. These are organic compounds containing a sulfonamide group that is S-linked to a benzene ring.
KingdomOrganic compounds
Super ClassBenzenoids
ClassBenzene and substituted derivatives
Sub ClassBenzenesulfonamides
Direct ParentBenzenesulfonamides
Alternative Parents
Substituents
  • Benzenesulfonamide
  • Tosyl compound
  • Benzenesulfonyl group
  • Toluene
  • Organic sulfonic acid or derivatives
  • Organosulfonic acid or derivatives
  • Sulfonyl
  • Organic metal halide
  • Organic alkali metal salt
  • Organic sodium salt
  • Organic salt
  • Organic oxygen compound
  • Organosulfur compound
  • Organic nitrogen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
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 Solubility1.52 g/LALOGPS
logP-1.2ALOGPS
logP1.85ChemAxon
logS-2.2ALOGPS
pKa (Strongest Acidic)4.89ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area43.37 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity47.79 m³·mol⁻¹ChemAxon
Polarizability18.99 ųChemAxon
Number of Rings1ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
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 IDDBSALT001646
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 IDNot Available
PubChem Compound ID517414
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available