<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-03-31 19:48:50 UTC</creation_date>
  <update_date>2026-08-22 09:36:59 UTC</update_date>
  <accession/>
  <common_name>1H-1,2,3-Triazole</common_name>
  <class>SmallMolecule</class>
  <description>1H-1,2,3-Triazole is an organic compound with the chemical formula C2H3N3 and an average molecular weight of 69.07 g/mol. 1H-1,2,3-Triazole belongs to the triazoles, a subclass of azoles within the organic compounds. Within the broader chemical hierarchy, it is categorized under the superclass of organoheterocyclic compounds.

This compound has been identified in or released from 23 recorded sources. In the sector of electrical and electronic equipment, it is associated with antennas, auxiliary devices, communication cables or conductors, cores yokes or armatures, and discharge lamps, among eight other sources. It is also found in building and construction materials, specifically in ceilings, fencing, roofs, and tents or canopies. Additionally, the compound is linked to food, food processing and cookware, where it appears in fermentation processes for beer as well as the processing of fish and meats. Finally, 1H-1,2,3-Triazole is present in household cleaning and consumer products, including cigar cigarettes, non electric simulated smoking devices, and tobacco product cases.</description>
  <categories/>
  <types/>
  <synonyms>
    <synonym>1,2,3 triazole</synonym>
    <synonym>1,2,3-1H-Triazole</synonym>
    <synonym>1,2,3-2H-triazole</synonym>
    <synonym>1,2,3-triazol</synonym>
    <synonym>1,2,3-Triazole</synonym>
    <synonym>1H-1,2,3-Triazol</synonym>
    <synonym>1H-1,2,3-Triazole</synonym>
    <synonym>1H-1,2,3-Triazole 98%</synonym>
    <synonym>1H-imidazole, 2-ethyl-5-methyl-</synonym>
    <synonym>1H-triazole</synonym>
    <synonym>1H-[1,2,3]Triazole</synonym>
    <synonym>206-022-9</synonym>
    <synonym>2H-1,2,3-TRIAZOLE</synonym>
    <synonym>2H-triazole</synonym>
    <synonym>4-amino-N-(5-methyl-3-isoxazolyl)benzene sulfonamide</synonym>
    <synonym>Gantanol</synonym>
    <synonym>M'1-(5-methylisoxazole-3-yl)sulfanilamide</synonym>
    <synonym>N1-(5-methyl-3-isoxazolyl)benzenesulfonamide</synonym>
    <synonym>OR-0596</synonym>
    <synonym>osotriazole</synonym>
    <synonym>PYRRODIAZOLE</synonym>
    <synonym>Radonil</synonym>
    <synonym>s-Triazole</synonym>
    <synonym>Sinomin</synonym>
    <synonym>sulfamethou000du000axazol</synonym>
    <synonym>Sulfamethoxazole</synonym>
    <synonym>Sulphamethoxazole</synonym>
    <synonym>T5MNNJ</synonym>
    <synonym>TL806300</synonym>
    <synonym>Triazacyclopentadiene</synonym>
    <synonym>triazol</synonym>
    <synonym>triazole</synonym>
    <synonym>V-triazole</synonym>
    <synonym>[1,2,3]-triazole</synonym>
    <synonym>[288-36-8]</synonym>
  </synonyms>
  <chemical_formula>C2H3N3</chemical_formula>
  <average_molecular_weight>69.067</average_molecular_weight>
  <monisotopic_moleculate_weight>69.032697</monisotopic_moleculate_weight>
  <iupac_name>2H-1,2,3-triazole</iupac_name>
  <traditional_iupac>2H-1,2,3-triazole</traditional_iupac>
  <cas_registry_number>288-36-8;288-35-7;27070-49-1;37306-44-8</cas_registry_number>
  <smiles>N1N=CC=N1</smiles>
  <inchi>InChI=1S/C2H3N3/c1-2-4-5-3-1/h1-2H,(H,3,4,5)</inchi>
  <inchikey>QWENRTYMTSOGBR-UHFFFAOYSA-N</inchikey>
  <taxonomy>
    <kingdom>Organic compounds</kingdom>
    <super_class>Organoheterocyclic compounds</super_class>
    <class>Azoles</class>
    <sub_class>Triazoles</sub_class>
    <direct_parent>Triazoles</direct_parent>
    <alternate_parents>
      <alternative_parent>Azacyclic compounds</alternative_parent>
      <alternative_parent>Heteroaromatic compounds</alternative_parent>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>Organonitrogen compounds</alternative_parent>
      <alternative_parent>Organopnictogen compounds</alternative_parent>
    </alternate_parents>
    <substituents>
      <substituent>1,2,3-triazole</substituent>
      <substituent>Aromatic heteromonocyclic compound</substituent>
      <substituent>Azacycle</substituent>
      <substituent>Heteroaromatic compound</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Organic nitrogen compound</substituent>
      <substituent>Organonitrogen compound</substituent>
      <substituent>Organopnictogen compound</substituent>
    </substituents>
    <molecular_framework>Aromatic heteromonocyclic compounds</molecular_framework>
    <descriptors>
      <descriptor>1,2,3-triazole</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>-0.3</value>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>logp</kind>
      <value>-0.53</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logs</kind>
      <value>0.91</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>solubility</kind>
      <value>5.58e+02 g/l</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logp</kind>
      <value>-0.5</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_acidic</kind>
      <value>9.09</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_basic</kind>
      <value>0.31</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>iupac</kind>
      <value>2H-1,2,3-triazole</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>average_mass</kind>
      <value>69.067</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>69.032697</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>N1N=CC=N1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C2H3N3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C2H3N3/c1-2-4-5-3-1/h1-2H,(H,3,4,5)</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>QWENRTYMTSOGBR-UHFFFAOYSA-N</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polar_surface_area</kind>
      <value>41.57</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>refractivity</kind>
      <value>18.67</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polarizability</kind>
      <value>5.9</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>rotatable_bond_count</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>acceptor_count</kind>
      <value>2</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>67516</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>60839</chemspider_id>
  <kegg_id/>
  <uniprot_id/>
  <omim_id/>
  <chebi_id/>
  <biocyc_id/>
  <ctd_id/>
  <stitch_id/>
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  <wikipidia/>
  <general_references/>
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  </targets>
</compound>
