<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-03-31 22:44:10 UTC</creation_date>
  <update_date>2026-05-20 17:02:54 UTC</update_date>
  <accession/>
  <common_name>(2E,6E)-Nona-2,6-dien-1-ol</common_name>
  <class>SmallMolecule</class>
  <description>(2E,6E)-Nona-2,6-dien-1-ol belongs to the fatty alcohols, a subclass of fatty acyls within the organic compounds. This compound has the chemical formula C9H16O1. It is categorized under the superclass of lipids and lipid-like molecules. (2E,6E)-Nona-2,6-dien-1-ol has been identified in one recorded source, specifically within household cleaning and consumer products, including tobacco product cases.</description>
  <categories/>
  <types/>
  <synonyms>
    <synonym>(2E,6E)-2,6-Nonadien-1-ol</synonym>
    <synonym>(2E,6E)-Nona-2,6-dien-1-ol</synonym>
    <synonym>(2E,6Z)-Nona-2,6-dien-1-ol</synonym>
    <synonym>(E,Z)-2,6-Nonadien-1-ol</synonym>
    <synonym>(E,Z)-2,6-nonadienol</synonym>
    <synonym>2,6-NODIENOL</synonym>
    <synonym>2,6-Nonadien-1-ol, (2E,6E)-</synonym>
    <synonym>2,6-Nonadien-1-ol, (2E,6Z)-</synonym>
    <synonym>2,6-Nonadien-1-ol, (E,Z)-</synonym>
    <synonym>2,6-Nonadien-1-ol,(2E,6Z)-</synonym>
    <synonym>2-trans-6-cis-Nonadien-1-ol</synonym>
    <synonym>227-394-9</synonym>
    <synonym>232-097-2</synonym>
    <synonym>248-816-8</synonym>
    <synonym>Cucumber alcohol</synonym>
    <synonym>e,z-2,6-nonadien-1-ol FCC, No Antioxidant</synonym>
    <synonym>Nonadienol</synonym>
    <synonym>trans,cis-2,6-nonadien-1-ol</synonym>
    <synonym>Violet-leaf alcohol</synonym>
  </synonyms>
  <chemical_formula>C9H16O1</chemical_formula>
  <average_molecular_weight/>
  <monisotopic_moleculate_weight>140.120115</monisotopic_moleculate_weight>
  <iupac_name>(2Z,6Z)-nona-2,6-dien-1-ol</iupac_name>
  <traditional_iupac>(2Z,6Z)-nona-2,6-dien-1-ol</traditional_iupac>
  <cas_registry_number>5820-89-3</cas_registry_number>
  <smiles/>
  <inchi>InChI=1S/C9H16O/c1-2-3-4-5-6-7-8-9-10/h3-4,7-8,10H,2,5-6,9H2,1H3/b4-3+,8-7+</inchi>
  <inchikey>AMXYRHBJZOVHOL-DYWGDJMRSA-N</inchikey>
  <taxonomy>
    <kingdom>Organic compounds</kingdom>
    <super_class>Lipids and lipid-like molecules</super_class>
    <class>Fatty Acyls</class>
    <sub_class>Fatty alcohols</sub_class>
    <direct_parent>Fatty alcohols</direct_parent>
    <alternate_parents>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>Primary alcohols</alternative_parent>
    </alternate_parents>
    <substituents>
      <substituent>Alcohol</substituent>
      <substituent>Aliphatic acyclic compound</substituent>
      <substituent>Fatty alcohol</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Organic oxygen compound</substituent>
      <substituent>Organooxygen compound</substituent>
      <substituent>Primary alcohol</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/>
  <predicted_properties>
    <property>
      <kind>logp</kind>
      <value>3.13</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logs</kind>
      <value>-2.58</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>solubility</kind>
      <value>3.68e-01 g/l</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logp</kind>
      <value>2.46</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_acidic</kind>
      <value>16.08</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_basic</kind>
      <value>-2.3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>iupac</kind>
      <value>(2Z,6Z)-nona-2,6-dien-1-ol</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>140.120115</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C9H16O1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C9H16O/c1-2-3-4-5-6-7-8-9-10/h3-4,7-8,10H,2,5-6,9H2,1H3/b4-3+,8-7+</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>AMXYRHBJZOVHOL-DYWGDJMRSA-N</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polar_surface_area</kind>
      <value>20.23</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>refractivity</kind>
      <value>47.22</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polarizability</kind>
      <value>17.25</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>rotatable_bond_count</kind>
      <value>5</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>acceptor_count</kind>
      <value>1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>donor_count</kind>
      <value>1</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/>
  <mechanism_of_toxicity/>
  <metabolism/>
  <toxicity/>
  <lethaldose/>
  <carcinogenicity/>
  <use_source/>
  <min_risk_level/>
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  <symptoms/>
  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>5320191</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>4478338</chemspider_id>
  <kegg_id/>
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  <chebi_id/>
  <biocyc_id/>
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  <pdb_id/>
  <wikipidia/>
  <general_references/>
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</compound>
