<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">6729</id>
  <title nil="true"/>
  <common-name>ETHYL 2-HYDROXYETHYL SULFIDE</common-name>
  <description>ETHYL 2-HYDROXYETHYL SULFIDE is an organic compound with the formula C4H10OS and an average molecular weight of 106.18 g/mol. ETHYL 2-HYDROXYETHYL SULFIDE belongs to the dialkylthioethers, a subclass of thioethers within the organic compounds.

In industrial contexts, the compound is utilized as a nutrient and a flavouring agent. It has been identified in seven recorded sources, including drinking water and water supply systems. Within the food, food processing, and cookware sectors, it is associated with the processing of meats. It is also found in electrical and electronic equipment, specifically in electrodes and conductors or conductive bodies characterized by the conductive materials. Additionally, the compound is present in household cleaning and consumer products, such as soap detergents, bleaching agents, and perfumes within detergents and soaps. The recorded route of exposure for this substance is oral.</description>
  <cas>110-77-0</cas>
  <pubchem-id>8075</pubchem-id>
  <chemical-formula>C4H10OS</chemical-formula>
  <weight>106.19</weight>
  <appearance nil="true"/>
  <melting-point nil="true"/>
  <boiling-point nil="true"/>
  <density nil="true"/>
  <solubility nil="true"/>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure nil="true"/>
  <target nil="true"/>
  <mechanism-of-toxicity nil="true"/>
  <metabolism nil="true"/>
  <toxicity nil="true"/>
  <lethaldose nil="true"/>
  <carcinogenicity nil="true"/>
  <use-source nil="true"/>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms nil="true"/>
  <treatment nil="true"/>
  <created-at type="dateTime">2016-05-19T02:04:34Z</created-at>
  <updated-at type="dateTime">2026-08-22T15:32:34Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia nil="true"/>
  <uniprot-id nil="true"/>
  <kegg-compound-id nil="true"/>
  <omim-id nil="true"/>
  <chebi-id nil="true"/>
  <biocyc-id nil="true"/>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id nil="true"/>
  <pdb-id nil="true"/>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>CCSCCO</moldb-smiles>
  <moldb-formula>C4H10OS</moldb-formula>
  <moldb-inchi>InChI=1S/C4H10OS/c1-2-6-4-3-5/h5H,2-4H2,1H3</moldb-inchi>
  <moldb-inchikey>LNRIEBFNWGMXKP-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">106.18</moldb-average-mass>
  <moldb-mono-mass type="decimal">106.045236116</moldb-mono-mass>
  <origin nil="true"/>
  <state nil="true"/>
  <logp>0.6</logp>
  <hmdb-id nil="true"/>
  <chembl-id nil="true"/>
  <chemspider-id>21159459</chemspider-id>
  <structure-image-file-name nil="true"/>
  <structure-image-content-type nil="true"/>
  <structure-image-file-size type="integer" nil="true"/>
  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference nil="true"/>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM005624</chemdb-id>
  <dsstox-id>DTXSID3059393</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00003100</susdat-id>
  <iupac>2-ethylsulfanylethanol</iupac>
  <moldb-polar-surface-area>20.23</moldb-polar-surface-area>
  <moldb-refractivity>30.185000000000002</moldb-refractivity>
  <moldb-polarizability>12.277856481822946</moldb-polarizability>
  <moldb-rotatable-bond-count>3</moldb-rotatable-bond-count>
  <moldb-acceptor-count>1</moldb-acceptor-count>
  <moldb-donor-count>1</moldb-donor-count>
  <moldb-pka-strongest-acidic>15.547770141448968</moldb-pka-strongest-acidic>
  <moldb-pka-strongest-basic>-2.5592053401302213</moldb-pka-strongest-basic>
  <moldb-physiological-charge>0</moldb-physiological-charge>
  <moldb-number-of-rings>0</moldb-number-of-rings>
  <moldb-alogps-logp>0.61</moldb-alogps-logp>
  <moldb-alogps-logs>-0.51</moldb-alogps-logs>
  <moldb-alogps-solubility>3.26e+01 g/l</moldb-alogps-solubility>
  <kingdom>Organic compounds</kingdom>
  <superklass>Organosulfur compounds</superklass>
  <klass>Thioethers</klass>
  <subklass>Dialkylthioethers</subklass>
  <paper-count type="integer">17</paper-count>
  <sync-id>CED0008767</sync-id>
  <structure-inchikey>LNRIEBFNWGMXKP-UHFFFAOYSA-N</structure-inchikey>
  <structure-fingerprint>800000000800000000000400000000000002000000000000000002000000000080000080000000000000000000000000004000000000000000000000000000000000000000000000000000000000000000000000000000000000010000000000000000000000000000000008004000000000000000000000000040000000000000000000000000000002000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000020</structure-fingerprint>
  <structure-pattern-fingerprint>800002000000000000000000000000000004000000000040000000000000000000000000000000000000000000000000000400000000400000000000001100000000000000000000004200000000000000000002000000000000010000200000000000000000000000200000000000100000a00011000000001000020040000004000000040000000000000010040002000000000000080000004000404100000000000000000000000000000240000000000000000000000000000000000000200000000000000000000000000000000000000000000000080000000000000000000000000000000000000000000000000000000000000010000000</structure-pattern-fingerprint>
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</structure-pickle>
  <structure-indexed-at type="dateTime">2026-09-19T04:02:30Z</structure-indexed-at>
</compound>
