<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-04-03 11:59:00 UTC</creation_date>
  <update_date>2026-08-23 04:23:12 UTC</update_date>
  <accession/>
  <common_name>1-Ethylvinyl acetate</common_name>
  <class>SmallMolecule</class>
  <description>1-Ethylvinyl acetate is an organic compound with the formula C6H10O2 and an average molecular weight of 114.14 g/mol. 1-Ethylvinyl acetate belongs to the carboxylic acid derivatives, a subclass of carboxylic acids and derivatives within the organic compounds.

This substance is found in or released from 14 recorded sources across several categories. Within building and construction, it is associated with ceilings, fencing, floors, roofs, tents or canopies. In the realm of electrical and electronic equipment, it is linked to antennas, electric hearing aids, gas filled discharge tubes with solid cathode, and microphones. It is also present in food, food processing and cookware, specifically in the treatment of hops and the preparation of wine or sparkling wine. Additionally, it is found in household cleaning and consumer products, including tobacco product cases and non electric simulated smoking devices, as well as in household items such as watch chains.</description>
  <categories/>
  <types/>
  <synonyms>
    <synonym>1-Buten-2-ol, acetate</synonym>
    <synonym>1-Buten-2-yl acetate</synonym>
    <synonym>1-ethylvinyl acetate</synonym>
    <synonym>234-029-7</synonym>
    <synonym>But-1-en-2-yl acetate</synonym>
  </synonyms>
  <chemical_formula>C6H10O2</chemical_formula>
  <average_molecular_weight>114.144</average_molecular_weight>
  <monisotopic_moleculate_weight>114.06808</monisotopic_moleculate_weight>
  <iupac_name/>
  <traditional_iupac/>
  <cas_registry_number>10500-08-0</cas_registry_number>
  <smiles>CCC(=C)OC(C)=O</smiles>
  <inchi>InChI=1S/C6H10O2/c1-4-5(2)8-6(3)7/h2,4H2,1,3H3</inchi>
  <inchikey>BVCLXNHIJBDDTH-UHFFFAOYSA-N</inchikey>
  <taxonomy>
    <kingdom>Organic compounds</kingdom>
    <super_class>Organic acids and derivatives</super_class>
    <class>Carboxylic acids and derivatives</class>
    <sub_class>Carboxylic acid derivatives</sub_class>
    <direct_parent>Enol esters</direct_parent>
    <alternate_parents>
      <alternative_parent>Carbonyl compounds</alternative_parent>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>Monocarboxylic acids and derivatives</alternative_parent>
      <alternative_parent>Organic oxides</alternative_parent>
    </alternate_parents>
    <substituents>
      <substituent>Aliphatic acyclic compound</substituent>
      <substituent>Carbonyl group</substituent>
      <substituent>Enol ester</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Monocarboxylic acid or derivatives</substituent>
      <substituent>Organic oxide</substituent>
      <substituent>Organic oxygen compound</substituent>
      <substituent>Organooxygen compound</substituent>
    </substituents>
    <molecular_framework>Aliphatic acyclic 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>1.4</value>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>average_mass</kind>
      <value>114.144</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>114.06808</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>CCC(=C)OC(C)=O</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C6H10O2</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C6H10O2/c1-4-5(2)8-6(3)7/h2,4H2,1,3H3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>BVCLXNHIJBDDTH-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:0x00007f3bafb19e40&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>82680</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>74613</chemspider_id>
  <kegg_id/>
  <uniprot_id/>
  <omim_id/>
  <chebi_id/>
  <biocyc_id/>
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  <wikipidia/>
  <general_references/>
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</compound>
