<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-04-04 07:55:19 UTC</creation_date>
  <update_date>2026-08-24 11:47:11 UTC</update_date>
  <accession/>
  <common_name>(Ethylthio)benzene</common_name>
  <class>SmallMolecule</class>
  <description>(Ethylthio)benzene is an organosulfur compound with the chemical formula C8H10S1 and an average molecular weight of 138.23 g/mol. (Ethylthio)benzene belongs to the aryl thioethers, a subclass of thioethers within the organic compounds.

This substance is found in or released from seven recorded sources across several sectors. Within the category of electrical and electronic equipment, it is associated with antennas, conductors or conductive bodies characterised by the conductive materials, fixed capacitors and their manufacture, hybrid capacitors, and television systems. In the context of food, food processing and cookware, the compound is linked to fermentation processes for beer. Additionally, it is found in household cleaning and consumer products, specifically within perfumes used in detergents and soaps.</description>
  <categories/>
  <types/>
  <synonyms>
    <synonym>(1-Thiapropyl)benzene</synonym>
    <synonym>(Ethylsulfanyl)benzene</synonym>
    <synonym>(Ethylsulfanyl)benzol</synonym>
    <synonym>(Ethylthio)benzene</synonym>
    <synonym>(Phenylthio)ethane</synonym>
    <synonym>16M</synonym>
    <synonym>1905731</synonym>
    <synonym>622388</synonym>
    <synonym>Benzene, (ethylthio)-</synonym>
    <synonym>Benzene, (ethylthio)- (9CI)</synonym>
    <synonym>Ethyl phenyl sulfide</synonym>
    <synonym>Ethyl phenyl sulphide</synonym>
    <synonym>ethyl(phenyl)sulfane</synonym>
    <synonym>ethylphenyl sulfide</synonym>
    <synonym>ETHYLPHENYLSULFIDE</synonym>
    <synonym>ethylsulfanylbenzene</synonym>
    <synonym>Ethylthiobenzene</synonym>
    <synonym>Phenyl ethyl sulfide</synonym>
    <synonym>Phenyl(ethyl)sulfide</synonym>
    <synonym>Phenylethyl sulfide</synonym>
    <synonym>phenylethylthiol</synonym>
    <synonym>Sulfide, ethyl phenyl</synonym>
    <synonym>Sulfide, ethyl phenyl (8CI)</synonym>
    <synonym>Thiophenetole</synonym>
    <synonym>TL8004071</synonym>
    <synonym>[622-38-8]</synonym>
  </synonyms>
  <chemical_formula>C8H10S1</chemical_formula>
  <average_molecular_weight>138.23</average_molecular_weight>
  <monisotopic_moleculate_weight>138.050321</monisotopic_moleculate_weight>
  <iupac_name/>
  <traditional_iupac/>
  <cas_registry_number>622-38-8</cas_registry_number>
  <smiles>CCSC1=CC=CC=C1</smiles>
  <inchi>InChI=1S/C8H10S/c1-2-9-8-6-4-3-5-7-8/h3-7H,2H2,1H3</inchi>
  <inchikey>AEHWKBXBXYNPCX-UHFFFAOYSA-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>
    <property>
      <kind>logp</kind>
      <value>3.2</value>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>average_mass</kind>
      <value>138.23</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>138.050321</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>CCSC1=CC=CC=C1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C8H10S1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C8H10S/c1-2-9-8-6-4-3-5-7-8/h3-7H,2H2,1H3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>AEHWKBXBXYNPCX-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:0x00007f3bafc37638&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>12144</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>11645</chemspider_id>
  <kegg_id/>
  <uniprot_id/>
  <omim_id/>
  <chebi_id/>
  <biocyc_id/>
  <ctd_id/>
  <stitch_id/>
  <actor_id/>
  <pdb_id/>
  <wikipidia/>
  <general_references/>
  <targets>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
  </targets>
</compound>
