<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-03-31 21:21:14 UTC</creation_date>
  <update_date>2026-05-20 19:30:05 UTC</update_date>
  <accession/>
  <common_name>Disulon</common_name>
  <class>SmallMolecule</class>
  <description>Disulon is an organic compound with the chemical formula C12H13N3O4S2. Disulon belongs to the benzenesulfonamides, a subclass of benzene and substituted derivatives within the organic compounds. This substance is categorized as a benzenoid. It has been identified in one recorded source: healthcare, pharmaceuticals &amp; veterinary products, specifically as an antibiotic. Recorded exposure routes for this compound include inhalation and oral ingestion.</description>
  <categories/>
  <types/>
  <synonyms>
    <synonym>4'-Sulfamoylsulfanilanilide</synonym>
    <synonym>4-(4'-Aminobenzenesulfonamido)benzenesulfonamide</synonym>
    <synonym>4-(4-aminophenylsulfonamido)-1-benzenesulfonamide</synonym>
    <synonym>4-amino-bis-benzenesulfonamide</synonym>
    <synonym>4-Amino-N-(4-sulfamoylphenyl)benzenesulfonamide</synonym>
    <synonym>4-amino-N-[4-(aminosulfonyl)phenyl]benzenesulfonamide</synonym>
    <synonym>4-Aminobenzenesulfono-p-sulfamoylanilide</synonym>
    <synonym>4-[(4-aminophenyl)sulfonylamino]benzenesulfonamide</synonym>
    <synonym>4-{[(4-aminophenyl)sulfonyl]amino}benzenesulfonamide</synonym>
    <synonym>Albasil C</synonym>
    <synonym>ARONIS022694</synonym>
    <synonym>Benzenesulfonamide, 4-amino-N-(4-(aminosulfonyl)phenyl)-</synonym>
    <synonym>Benzenesulfonamide, 4-amino-N-[4-(aminosulfonyl)phenyl]-</synonym>
    <synonym>CHEMBL269122</synonym>
    <synonym>Diseptal C</synonym>
    <synonym>Disulon</synonym>
    <synonym>disulphane</synonym>
    <synonym>L-572,787-00Y</synonym>
    <synonym>MFCD02575824</synonym>
    <synonym>N(4)-Sulfanilylsulfanilamide</synonym>
    <synonym>N1-(4-SO2NH2-PH)SULFANILAMIDE</synonym>
    <synonym>N4-Sulfanilylsulfanilamide</synonym>
    <synonym>Neosanamid II</synonym>
    <synonym>ST040798</synonym>
    <synonym>Uliron C</synonym>
    <synonym>UNII-HKA2A1D99J</synonym>
    <synonym>UNII:HKA2A1D99J</synonym>
  </synonyms>
  <chemical_formula>C12H13N3O4S2</chemical_formula>
  <average_molecular_weight/>
  <monisotopic_moleculate_weight>327.034747</monisotopic_moleculate_weight>
  <iupac_name/>
  <traditional_iupac/>
  <cas_registry_number>547-52-4</cas_registry_number>
  <smiles/>
  <inchi>InChI=1S/C12H13N3O4S2/c13-9-1-5-12(6-2-9)21(18,19)15-10-3-7-11(8-4-10)20(14,16)17/h1-8,15H,13H2,(H2,14,16,17)</inchi>
  <inchikey>GCQZFVAHUZIDRP-UHFFFAOYSA-N</inchikey>
  <taxonomy>
    <kingdom>Organic compounds</kingdom>
    <super_class>Benzenoids</super_class>
    <class>Benzene and substituted derivatives</class>
    <sub_class>Benzenesulfonamides</sub_class>
    <direct_parent>Aminobenzenesulfonamides</direct_parent>
    <alternate_parents>
      <alternative_parent>Aminosulfonyl compounds</alternative_parent>
      <alternative_parent>Aniline and substituted anilines</alternative_parent>
      <alternative_parent>Benzenesulfonyl compounds</alternative_parent>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>Organic oxides</alternative_parent>
      <alternative_parent>Organopnictogen compounds</alternative_parent>
      <alternative_parent>Organosulfonamides</alternative_parent>
      <alternative_parent>Primary amines</alternative_parent>
      <alternative_parent>Sulfanilides</alternative_parent>
    </alternate_parents>
    <substituents>
      <substituent>Amine</substituent>
      <substituent>Aminobenzenesulfonamide</substituent>
      <substituent>Aminosulfonyl compound</substituent>
      <substituent>Aniline or substituted anilines</substituent>
      <substituent>Aromatic homomonocyclic compound</substituent>
      <substituent>Benzenesulfonyl group</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Organic nitrogen compound</substituent>
      <substituent>Organic oxide</substituent>
      <substituent>Organic oxygen compound</substituent>
      <substituent>Organic sulfonic acid or derivatives</substituent>
      <substituent>Organonitrogen compound</substituent>
      <substituent>Organopnictogen compound</substituent>
      <substituent>Organosulfonic acid amide</substituent>
      <substituent>Organosulfonic acid or derivatives</substituent>
      <substituent>Organosulfur compound</substituent>
      <substituent>Primary amine</substituent>
      <substituent>Sulfanilide</substituent>
      <substituent>Sulfonyl</substituent>
    </substituents>
    <molecular_framework>Aromatic homomonocyclic compounds</molecular_framework>
    <descriptors/>
  </taxonomy>
  <status>Detected and Not Quantified</status>
  <origin/>
  <cellular_locations/>
  <biofluid_locations/>
  <tissue_locations/>
  <pathways/>
  <state/>
  <appearance/>
  <experimental_properties/>
  <predicted_properties>
    <property>
      <kind>mono_mass</kind>
      <value>327.034747</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C12H13N3O4S2</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C12H13N3O4S2/c13-9-1-5-12(6-2-9)21(18,19)15-10-3-7-11(8-4-10)20(14,16)17/h1-8,15H,13H2,(H2,14,16,17)</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>GCQZFVAHUZIDRP-UHFFFAOYSA-N</value>
      <source>ChemAxon</source>
    </property>
  </predicted_properties>
  <route_of_exposure/>
  <mechanism_of_toxicity/>
  <metabolism/>
  <toxicity/>
  <lethaldose/>
  <carcinogenicity/>
  <use_source/>
  <min_risk_level/>
  <health_effects>#&lt;HealthEffect::ActiveRecord_Associations_CollectionProxy:0x00007f3baf5afab8&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>68351</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>61646</chemspider_id>
  <kegg_id/>
  <uniprot_id/>
  <omim_id/>
  <chebi_id/>
  <biocyc_id/>
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  <wikipidia/>
  <general_references/>
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</compound>
