<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-04-03 22:21:01 UTC</creation_date>
  <update_date>2026-08-23 21:43:18 UTC</update_date>
  <accession/>
  <common_name>Cyclohexanemethylamine</common_name>
  <class>SmallMolecule</class>
  <description>Cyclohexanemethylamine is an organic nitrogen compound with the chemical formula C7H15N1 and an average molecular weight of 113.20 g/mol. Cyclohexanemethylamine belongs to the amines, a subclass of organonitrogen compounds within the organic compounds.

This compound is found in or released from nine recorded sources across three primary categories. Within electrical and electronic equipment, it is associated with antennas, coils, emergency protective devices, still video cameras, and superconducting magnets and superconducting coils. In the context of food, food processing, and cookware, it is linked to the preparation of wort, fermentation processes for beer, and the treatment of hops. Additionally, it is recorded in building and construction sources, specifically regarding fencing.</description>
  <categories/>
  <types/>
  <synonyms>
    <synonym>(Aminomethyl)cyclohexane</synonym>
    <synonym>(Aminomethyl)cyclohexane, Hexahydrobenzylamine</synonym>
    <synonym>08.02.3218</synonym>
    <synonym>08/02/18</synonym>
    <synonym>08/02/3218</synonym>
    <synonym>1-Cyclohexylmethanamine</synonym>
    <synonym>2/8/3218</synonym>
    <synonym>2/8/3218 12:00:00 AM</synonym>
    <synonym>3218-02--8</synonym>
    <synonym>3218/2/8</synonym>
    <synonym>50877-01-5, 3218-02-8, 7003-32-9</synonym>
    <synonym>635751</synonym>
    <synonym>AMC</synonym>
    <synonym>Aminomethylcyclohexane</synonym>
    <synonym>c-C6H11CH2NH2</synonym>
    <synonym>C-Cyclohexyl-methylamine</synonym>
    <synonym>CHEMBL1049</synonym>
    <synonym>Cyclohexane</synonym>
    <synonym>CYCLOHEXANE METHYLAMINE</synonym>
    <synonym>Cyclohexanemethanamine</synonym>
    <synonym>Cyclohexanemethylamine</synonym>
    <synonym>CyclohexYl-Methanamine</synonym>
    <synonym>cyclohexylmethanamine</synonym>
    <synonym>cyclohexylmethylamine</synonym>
    <synonym>DECARBOXYLATED DERIVATIVE</synonym>
    <synonym>Gabapentin</synonym>
    <synonym>Hexahydrobenzylamine</synonym>
    <synonym>[3218-02-8]</synonym>
  </synonyms>
  <chemical_formula>C7H15N1</chemical_formula>
  <average_molecular_weight>113.204</average_molecular_weight>
  <monisotopic_moleculate_weight>113.120449</monisotopic_moleculate_weight>
  <iupac_name/>
  <traditional_iupac/>
  <cas_registry_number>08-02-18</cas_registry_number>
  <smiles>NCC1CCCCC1</smiles>
  <inchi>InChI=1S/C7H15N/c8-6-7-4-2-1-3-5-7/h7H,1-6,8H2</inchi>
  <inchikey>AVKNGPAMCBSNSO-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>1.7</value>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>average_mass</kind>
      <value>113.204</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>113.120449</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>NCC1CCCCC1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C7H15N1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C7H15N/c8-6-7-4-2-1-3-5-7/h7H,1-6,8H2</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>AVKNGPAMCBSNSO-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:0x00007f7224221378&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>76688</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>69149</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>
