<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2016-05-19 04:48:55 UTC</creation_date>
  <update_date>2026-04-17 19:28:39 UTC</update_date>
  <accession/>
  <common_name>1,2,3-Benzenetriol</common_name>
  <class>SmallMolecule</class>
  <description>1,2,3-Benzenetriol is an organic compound with the chemical formula C6H6O3 and an average molecular weight of 126.11 g/mol. 1,2,3-Benzenetriol belongs to the benzenetriols and derivatives, a subclass of phenols within the organic compounds. It is classified as part of the benzenoids superclass. Industrially, the compound is used as a dye.

The substance is found in or released from 51 recorded sources across multiple sectors. Within electrical and electronic equipment, it is associated with cell phones, capacitors, batteries, printed circuit boards, and wires and cables, among 21 other sources. In the realm of food, food processing, and cookware, it is linked to food packaging, food contact materials, cellar tools, food preservation, and fermentation processes for beer, as well as five additional sources. Household cleaning and consumer products containing the compound include bleaching agents, soap detergents, perfumes within detergents and soaps, cigar cigarettes, and tobacco pipes, plus one other source. In building and construction, it is found in ladders, ceilings, and tents or canopies. It is also present in synthetic textiles, carpets and rugs within the textiles, leather, and furnishings sector, and in medical devices within healthcare, pharmaceuticals, and veterinary products, along with three more sectors. Recorded exposure routes for 1,2,3-Benzenetriol include touch, oral, and inhalation.</description>
  <categories/>
  <types>
    <type>PFAS</type>
    <type>Phytotoxin</type>
  </types>
  <synonyms>
    <synonym>1,2,3-Trihydroxybenzene</synonym>
    <synonym>Pyrogallol</synonym>
  </synonyms>
  <chemical_formula>C6H6O3</chemical_formula>
  <average_molecular_weight>126.11</average_molecular_weight>
  <monisotopic_moleculate_weight>126.031694058</monisotopic_moleculate_weight>
  <iupac_name>benzene-1,2,3-triol</iupac_name>
  <traditional_iupac>pyrogallol</traditional_iupac>
  <cas_registry_number>87-66-1</cas_registry_number>
  <smiles>OC1=CC=CC(O)=C1O</smiles>
  <inchi>InChI=1S/C6H6O3/c7-4-2-1-3-5(8)6(4)9/h1-3,7-9H</inchi>
  <inchikey>WQGWDDDVZFFDIG-UHFFFAOYSA-N</inchikey>
  <taxonomy>
    <kingdom>Organic compounds</kingdom>
    <super_class>Benzenoids</super_class>
    <class>Phenols</class>
    <sub_class>Benzenetriols and derivatives</sub_class>
    <direct_parent>5-unsubstituted pyrrogallols</direct_parent>
    <alternate_parents>
      <alternative_parent>1-hydroxy-2-unsubstituted benzenoids</alternative_parent>
      <alternative_parent>1-hydroxy-4-unsubstituted benzenoids</alternative_parent>
      <alternative_parent>Benzene and substituted derivatives</alternative_parent>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>Polyols</alternative_parent>
    </alternate_parents>
    <substituents>
      <substituent>1-hydroxy-2-unsubstituted benzenoid</substituent>
      <substituent>1-hydroxy-4-unsubstituted benzenoid</substituent>
      <substituent>5-unsubstituted pyrrogallol</substituent>
      <substituent>Aromatic homomonocyclic compound</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Monocyclic benzene moiety</substituent>
      <substituent>Organic oxygen compound</substituent>
      <substituent>Organooxygen compound</substituent>
      <substituent>Polyol</substituent>
    </substituents>
    <molecular_framework>Aromatic homomonocyclic compounds</molecular_framework>
    <descriptors>
      <descriptor>Gallotannins</descriptor>
      <descriptor>a small molecule</descriptor>
      <descriptor>benzenetriol</descriptor>
    </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>0.34</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logs</kind>
      <value>-0.39</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>solubility</kind>
      <value>5.18e+01 g/l</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logp</kind>
      <value>1.06</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_acidic</kind>
      <value>8.94</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_basic</kind>
      <value>-6</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>iupac</kind>
      <value>benzene-1,2,3-triol</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>average_mass</kind>
      <value>126.11</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>126.031694058</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>OC1=CC=CC(O)=C1O</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C6H6O3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C6H6O3/c7-4-2-1-3-5(8)6(4)9/h1-3,7-9H</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>WQGWDDDVZFFDIG-UHFFFAOYSA-N</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polar_surface_area</kind>
      <value>60.69</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>refractivity</kind>
      <value>32</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polarizability</kind>
      <value>11.57</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>rotatable_bond_count</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>acceptor_count</kind>
      <value>3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>donor_count</kind>
      <value>3</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/>
  <health_effects>#&lt;HealthEffect::ActiveRecord_Associations_CollectionProxy:0x00007f3bcf50dcc0&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>1057</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>11381</chemspider_id>
  <kegg_id/>
  <uniprot_id/>
  <omim_id/>
  <chebi_id/>
  <biocyc_id/>
  <ctd_id/>
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  <pdb_id/>
  <wikipidia/>
  <general_references/>
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</compound>
