<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-03-27 00:58:33 UTC</creation_date>
  <update_date>2026-08-19 17:58:57 UTC</update_date>
  <accession/>
  <common_name>Tetrabutylammonium</common_name>
  <class>SmallMolecule</class>
  <description>Tetrabutylammonium is an organic nitrogen compound with the chemical formula C16H36N1 and an average molecular weight of 242.47 g/mol. Tetrabutylammonium belongs to the quaternary ammonium salts, a subclass of organonitrogen compounds within the organic compounds.

This compound is found in or released from 15 recorded sources across various sectors. Within electrical and electronic equipment, it is associated with antennas, discharge lamps, electric switches, emergency protective devices, and fixed capacitors and their manufacture, among four other sources. In the building and construction sector, it is linked to stairs and ramps as well as tents or canopies. Its presence is also noted in food, food processing and cookware, specifically regarding the preparation of wort and fermentation processes for beer. Additionally, it is found in household cleaning and consumer products, including soap detergents and bleaching agents.

In terms of biological interaction, there are two recorded protein targets for tetrabutylammonium: the immunoglobulin kappa constant (IGKC) and the pH-gated potassium channel KcsA (kcsA).</description>
  <categories/>
  <types/>
  <synonyms>
    <synonym>1-(Carbamoylmethyl)-1ÃƒÂ¢Ã‚â‚¬Ã‚Â²-methyl-4,4ÃƒÂ¢Ã‚â‚¬Ã‚Â²-bipyridinium bis(hexafluorophosphate)</synonym>
    <synonym>1-Butanaminium, N,N,N-tributyl-</synonym>
    <synonym>ammonium ion, tetrabutyl-</synonym>
    <synonym>benzyl triphenylphosphonium</synonym>
    <synonym>CBU2X6BBJR</synonym>
    <synonym>InChI=1/C16H36N/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4/h5-16H2,1-4H3/q+</synonym>
    <synonym>N,N,N-Tributyl-1-butanaminium</synonym>
    <synonym>N,N,N-Tributylbutan-1-aminium</synonym>
    <synonym>TBA</synonym>
    <synonym>tetra-n-butyl ammonium</synonym>
    <synonym>tetra-n-butylammonium</synonym>
    <synonym>Tetra-N-butylammoniumjodid</synonym>
    <synonym>tetrabutyl ammonium</synonym>
    <synonym>tetrabutylammonium</synonym>
    <synonym>Tetrabutylammonium cation</synonym>
    <synonym>Tetrabutylammonium ion</synonym>
    <synonym>tetrabutylazanium</synonym>
    <synonym>UNII-CBU2X6BBJR</synonym>
    <synonym>UNII:CBU2X6BBJR</synonym>
  </synonyms>
  <chemical_formula>C16H36N1</chemical_formula>
  <average_molecular_weight>242.47</average_molecular_weight>
  <monisotopic_moleculate_weight>242.284775</monisotopic_moleculate_weight>
  <iupac_name>tetrabutylazanium</iupac_name>
  <traditional_iupac>tetrabutylammonium</traditional_iupac>
  <cas_registry_number>10549-76-5</cas_registry_number>
  <smiles>CCCC[N+](CCCC)(CCCC)CCCC</smiles>
  <inchi>InChI=1S/C16H36N/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4/h5-16H2,1-4H3/q+1</inchi>
  <inchikey>DZLFLBLQUQXARW-UHFFFAOYSA-N</inchikey>
  <taxonomy>
    <kingdom>Organic compounds</kingdom>
    <super_class>Organic nitrogen compounds</super_class>
    <class>Organonitrogen compounds</class>
    <sub_class>Quaternary ammonium salts</sub_class>
    <direct_parent>Tetraalkylammonium salts</direct_parent>
    <alternate_parents>
      <alternative_parent>Amines</alternative_parent>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>Organic cations</alternative_parent>
      <alternative_parent>Organic salts</alternative_parent>
      <alternative_parent>Organopnictogen compounds</alternative_parent>
    </alternate_parents>
    <substituents>
      <substituent>Aliphatic acyclic compound</substituent>
      <substituent>Amine</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Organic cation</substituent>
      <substituent>Organic salt</substituent>
      <substituent>Organopnictogen compound</substituent>
      <substituent>Tetraalkylammonium salt</substituent>
    </substituents>
    <molecular_framework>Aliphatic acyclic compounds</molecular_framework>
    <descriptors>
      <descriptor>quaternary ammonium ion</descriptor>
    </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>5.3</value>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>logp</kind>
      <value>3.54</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logs</kind>
      <value>-7.39</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>solubility</kind>
      <value>1.14e-05 g/l</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logp</kind>
      <value>1.32</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>iupac</kind>
      <value>tetrabutylazanium</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>average_mass</kind>
      <value>242.47</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>242.284775</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>CCCC[N+](CCCC)(CCCC)CCCC</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C16H36N1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C16H36N/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4/h5-16H2,1-4H3/q+1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>DZLFLBLQUQXARW-UHFFFAOYSA-N</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polar_surface_area</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>refractivity</kind>
      <value>91.4</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polarizability</kind>
      <value>33.6</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>rotatable_bond_count</kind>
      <value>12</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>acceptor_count</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>donor_count</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>physiological_charge</kind>
      <value>1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formal_charge</kind>
      <value>1</value>
      <source>ChemAxon</source>
    </property>
  </predicted_properties>
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  <min_risk_level/>
  <health_effects>#&lt;HealthEffect::ActiveRecord_Associations_CollectionProxy:0x00007f7222747598&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id>DB01851</drugbank_id>
  <hmdb_id/>
  <pubchem_compound_id>16028</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>15220</chemspider_id>
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</compound>
