<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2016-05-19 03:05:51 UTC</creation_date>
  <update_date>2026-08-22 23:58:12 UTC</update_date>
  <accession/>
  <common_name>2,4-Imidazolidinedione, 1,3-dichloro-5,5-dimethyl-</common_name>
  <class>SmallMolecule</class>
  <description>2,4-Imidazolidinedione, 1,3-dichloro-5,5-dimethyl- (C5H6Cl2N2O2) is a chemical compound with an average molecular weight of 197.02 g/mol. 2,4-Imidazolidinedione, 1,3-dichloro-5,5-dimethyl- belongs to the imidazolidines, a subclass of azolidines within the organic compounds. Industrially, the substance serves as a biocide, preservative, and cleaning agent.

The compound is released from or found in 24 recorded sources. Within the category of electrical and electronic equipment, it is associated with antennas, coils, communication cables or conductors, conductive bodies characterised by the conductive materials, and colour television systems, among six others. In the realm of food, food processing, and cookware, it is linked to food preservation, the processing of meats and fish, and fermentation processes for beer and the preparation of wine or sparkling wine. Household cleaning and consumer product sources include soap detergents, soap dispensers, bleaching agents, perfumes within detergents and soaps, and tobacco smoke filters. Additionally, the compound is found in drinking water, tents or canopies used in building and construction, and pesticides used in agriculture and land management. Recorded exposure routes for this compound include oral and inhalation.</description>
  <categories/>
  <types>
    <type>Pesticide</type>
  </types>
  <synonyms>
    <synonym>1,3-Dichloro-5,5-dimethylhydantoin</synonym>
    <synonym>1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione</synonym>
    <synonym>1.3-Dichloro-5,5-dimethylhydantoin</synonym>
  </synonyms>
  <chemical_formula>C5H6Cl2N2O2</chemical_formula>
  <average_molecular_weight>197.02</average_molecular_weight>
  <monisotopic_moleculate_weight>195.9806328</monisotopic_moleculate_weight>
  <iupac_name>1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione</iupac_name>
  <traditional_iupac>1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione</traditional_iupac>
  <cas_registry_number>118-52-5</cas_registry_number>
  <smiles>CC1(C)N(Cl)C(=O)N(Cl)C1=O</smiles>
  <inchi>InChI=1S/C5H6Cl2N2O2/c1-5(2)3(10)8(6)4(11)9(5)7/h1-2H3</inchi>
  <inchikey>KEQGZUUPPQEDPF-UHFFFAOYSA-N</inchikey>
  <taxonomy>
    <kingdom>Organic compounds</kingdom>
    <super_class>Organoheterocyclic compounds</super_class>
    <class>Azolidines</class>
    <sub_class>Imidazolidines</sub_class>
    <direct_parent>Hydantoins</direct_parent>
    <alternate_parents>
      <alternative_parent>Alpha amino acids and derivatives</alternative_parent>
      <alternative_parent>Azacyclic compounds</alternative_parent>
      <alternative_parent>Carbonyl compounds</alternative_parent>
      <alternative_parent>Dicarboximides</alternative_parent>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>Organic carbonic acids and derivatives</alternative_parent>
      <alternative_parent>Organic oxides</alternative_parent>
      <alternative_parent>Organonitrogen compounds</alternative_parent>
      <alternative_parent>Organopnictogen compounds</alternative_parent>
    </alternate_parents>
    <substituents>
      <substituent>Aliphatic heteromonocyclic compound</substituent>
      <substituent>Alpha-amino acid or derivatives</substituent>
      <substituent>Azacycle</substituent>
      <substituent>Carbonic acid derivative</substituent>
      <substituent>Carbonyl group</substituent>
      <substituent>Carboxylic acid derivative</substituent>
      <substituent>Dicarboximide</substituent>
      <substituent>Hydantoin</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Organic nitrogen compound</substituent>
      <substituent>Organic oxide</substituent>
      <substituent>Organic oxygen compound</substituent>
      <substituent>Organonitrogen compound</substituent>
      <substituent>Organooxygen compound</substituent>
      <substituent>Organopnictogen compound</substituent>
    </substituents>
    <molecular_framework>Aliphatic heteromonocyclic compounds</molecular_framework>
    <descriptors/>
  </taxonomy>
  <status>Detected and Not Quantified</status>
  <origin/>
  <cellular_locations/>
  <biofluid_locations/>
  <tissue_locations/>
  <pathways/>
  <state/>
  <appearance/>
  <experimental_properties>
    <property>
      <kind>logp</kind>
      <value>1.1</value>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>logp</kind>
      <value>-1.48</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logs</kind>
      <value>-1.58</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>solubility</kind>
      <value>5.15e+00 g/l</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logp</kind>
      <value>1.08</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>iupac</kind>
      <value>1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>average_mass</kind>
      <value>197.02</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>195.9806328</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>CC1(C)N(Cl)C(=O)N(Cl)C1=O</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C5H6Cl2N2O2</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C5H6Cl2N2O2/c1-5(2)3(10)8(6)4(11)9(5)7/h1-2H3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>KEQGZUUPPQEDPF-UHFFFAOYSA-N</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polar_surface_area</kind>
      <value>40.62</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>refractivity</kind>
      <value>40.93</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polarizability</kind>
      <value>16.34</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>rotatable_bond_count</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>acceptor_count</kind>
      <value>2</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>donor_count</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>physiological_charge</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formal_charge</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
  </predicted_properties>
  <route_of_exposure/>
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  <use_source/>
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  <symptoms/>
  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>8360</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>8057</chemspider_id>
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</compound>
