<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2016-05-19 04:48:30 UTC</creation_date>
  <update_date>2026-04-05 17:46:03 UTC</update_date>
  <accession/>
  <common_name>Methanol, lithium salt</common_name>
  <class>SmallMolecule</class>
  <description>Methanol, lithium salt is an organic salt with the chemical formula CH3LiO and an average molecular weight of 37.97 g/mol. Methanol, lithium salt belongs to the organic alkali metal salts, a subclass of organic metal salts within the organic compounds.

This compound has been identified in or released from three recorded sources. These include building and construction materials, specifically tents or canopies, as well as electrical and electronic equipment, such as amplifiers and antennas.</description>
  <categories/>
  <types/>
  <synonyms/>
  <chemical_formula>CH3LiO</chemical_formula>
  <average_molecular_weight>37.97</average_molecular_weight>
  <monisotopic_moleculate_weight>38.03439316</monisotopic_moleculate_weight>
  <iupac_name>lithium(1+) ion methanolate</iupac_name>
  <traditional_iupac>lithium(1+) ion methoxide</traditional_iupac>
  <cas_registry_number>865-34-9</cas_registry_number>
  <smiles>[Li+].C[O-]</smiles>
  <inchi>InChI=1S/CH3O.Li/c1-2;/h1H3;/q-1;+1</inchi>
  <inchikey>JILPJDVXYVTZDQ-UHFFFAOYSA-N</inchikey>
  <taxonomy>
    <kingdom>Organic compounds</kingdom>
    <super_class>Organic salts</super_class>
    <class>Organic metal salts</class>
    <sub_class>Organic alkali metal salts</sub_class>
    <direct_parent>Organic lithium salts</direct_parent>
    <alternate_parents>
      <alternative_parent>Alkoxides</alternative_parent>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>Organic oxides</alternative_parent>
      <alternative_parent>Organic zwitterions</alternative_parent>
    </alternate_parents>
    <substituents>
      <substituent>Aliphatic acyclic compound</substituent>
      <substituent>Alkoxide</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Organic lithium salt</substituent>
      <substituent>Organic oxide</substituent>
      <substituent>Organic oxygen compound</substituent>
      <substituent>Organic zwitterion</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/>
  <predicted_properties>
    <property>
      <kind>logp</kind>
      <value>-0.41</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logs</kind>
      <value>0.94</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>solubility</kind>
      <value>3.34e+02 g/l</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logp</kind>
      <value>-0.52</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_acidic</kind>
      <value>15.78</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_basic</kind>
      <value>-2.5</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>iupac</kind>
      <value>lithium(1+) ion methanolate</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>average_mass</kind>
      <value>37.97</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>38.03439316</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>[Li+].C[O-]</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>CH3LiO</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/CH3O.Li/c1-2;/h1H3;/q-1;+1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>JILPJDVXYVTZDQ-UHFFFAOYSA-N</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polar_surface_area</kind>
      <value>23.06</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>refractivity</kind>
      <value>18.81</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polarizability</kind>
      <value>3.06</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>rotatable_bond_count</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>acceptor_count</kind>
      <value>1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>donor_count</kind>
      <value>0</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/>
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  <use_source/>
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  <health_effects>#&lt;HealthEffect::ActiveRecord_Associations_CollectionProxy:0x00007f3bafb83b60&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>4177230</pubchem_compound_id>
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</compound>
