<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-04-06 09:07:05 UTC</creation_date>
  <update_date>2026-05-21 09:13:58 UTC</update_date>
  <accession/>
  <common_name>Disopiramide</common_name>
  <class>SmallMolecule</class>
  <description>Disopiramide belongs to the pheniramines, a subclass of pyridines and derivatives within the organic compounds. This organoheterocyclic compound is associated with 15 recorded sources across multiple sectors. Within the healthcare, pharmaceuticals &amp; veterinary products sector, it is found in medical devices. In the energy, oil &amp; gas and industrial manufacturing &amp; chemical processing sectors, it is present in lubricants.

The compound is also released from electrical &amp; electronic equipment, including batteries, capacitors, printed circuit boards, wires and cables, and cell phones, among two other sources. It is found in food packaging within the food, food processing &amp; cookware sector, as well as in carpets, rugs, and synthetic textiles within the textiles, leather &amp; furnishings sector. Additionally, the compound is recorded in two other sectors. Exposure to disopiramide can occur through oral, inhalation, and touch routes.</description>
  <categories/>
  <types>
    <type>PFAS</type>
  </types>
  <synonyms/>
  <chemical_formula/>
  <average_molecular_weight/>
  <monisotopic_moleculate_weight/>
  <iupac_name/>
  <traditional_iupac/>
  <cas_registry_number>74464-84-9</cas_registry_number>
  <smiles/>
  <inchi>InChI=1S/C21H29N3O/c1-16(2)24(17(3)4)15-13-21(20(22)25,18-10-6-5-7-11-18)19-12-8-9-14-23-19/h5-12,14,16-17H,13,15H2,1-4H3,(H2,22,25)/t21-/m0/s1</inchi>
  <inchikey>UVTNFZQICZKOEM-NRFANRHFSA-N</inchikey>
  <taxonomy>
    <kingdom/>
    <super_class/>
    <class/>
    <sub_class/>
    <direct_parent/>
    <alternate_parents/>
    <substituents/>
    <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>inchi</kind>
      <value>InChI=1S/C21H29N3O/c1-16(2)24(17(3)4)15-13-21(20(22)25,18-10-6-5-7-11-18)19-12-8-9-14-23-19/h5-12,14,16-17H,13,15H2,1-4H3,(H2,22,25)/t21-/m0/s1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>UVTNFZQICZKOEM-NRFANRHFSA-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:0x00007f7225fae580&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>156295</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id/>
  <kegg_id/>
  <uniprot_id/>
  <omim_id/>
  <chebi_id/>
  <biocyc_id/>
  <ctd_id/>
  <stitch_id/>
  <actor_id/>
  <pdb_id/>
  <wikipidia/>
  <general_references/>
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</compound>
