<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-04-04 02:22:15 UTC</creation_date>
  <update_date>2026-08-22 13:10:00 UTC</update_date>
  <accession/>
  <common_name>1,3,5-Triazine-2,4-diamine</common_name>
  <class>SmallMolecule</class>
  <description>1,3,5-Triazine-2,4-diamine is an organic compound with the chemical formula C3H5N5 and an average molecular weight of 111.11 g/mol. 1,3,5-Triazine-2,4-diamine belongs to the 1,3,5-triazines, a subclass of triazines within the organic compounds.

The compound is found in or released from 31 recorded sources. Within the category of electrical and electronic equipment, it is associated with antennas, adjustable resistors, auxiliary devices, coils, and communication cables or conductors, among 16 other items. In household cleaning and consumer products, it appears in soap detergents, bleaching agents, perfumes within detergents and soaps, cigar cigarettes, and other smoking requisites, as well as one additional source. Furthermore, the substance is linked to building and construction materials, specifically tents or canopies and ladders. In the realm of food, food processing and cookware, it is found in processing meats and food preservation.</description>
  <categories/>
  <types/>
  <synonyms>
    <synonym>1, 3-Benzenediol, 5-methyl-</synonym>
    <synonym>1,3,5-Triazine-2,4-diamine</synonym>
    <synonym>2, 4-Diamino-s-triazine</synonym>
    <synonym>2,4-DIAMINO-1,3,5-TRIAZINE</synonym>
    <synonym>2,4-diamino-s-triazine</synonym>
    <synonym>2,4-Diaminotriazine (Related)</synonym>
    <synonym>2,6-diamino-s-triazine</synonym>
    <synonym>4, 6-Diamino-s-triazine</synonym>
    <synonym>4,6-diamino-s-triazine</synonym>
    <synonym>5-Methyl-1, 3-benzenediol</synonym>
    <synonym>5-Methylresorcin</synonym>
    <synonym>5/8/504</synonym>
    <synonym>8/5/504</synonym>
    <synonym>diamino-s-triazine</synonym>
    <synonym>formoguanamine</synonym>
    <synonym>guanamine</synonym>
    <synonym>Orcinol, 5-methylresorcinol</synonym>
    <synonym>s-Triazine, 2,4-diamino-</synonym>
    <synonym>s-Triazine, 2,4-diamino- (8CI)</synonym>
    <synonym>ZZS</synonym>
    <synonym>[1,3,5]Triazine-2,4-diamine</synonym>
    <synonym>[504-08-5]</synonym>
  </synonyms>
  <chemical_formula>C3H5N5</chemical_formula>
  <average_molecular_weight>111.108</average_molecular_weight>
  <monisotopic_moleculate_weight>111.054495</monisotopic_moleculate_weight>
  <iupac_name/>
  <traditional_iupac/>
  <cas_registry_number>504-08-5</cas_registry_number>
  <smiles>NC1=NC(N)=NC=N1</smiles>
  <inchi>InChI=1S/C3H5N5/c4-2-6-1-7-3(5)8-2/h1H,(H4,4,5,6,7,8)</inchi>
  <inchikey>VZXTWGWHSMCWGA-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>-0.7</value>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>average_mass</kind>
      <value>111.108</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>111.054495</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>NC1=NC(N)=NC=N1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C3H5N5</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C3H5N5/c4-2-6-1-7-3(5)8-2/h1H,(H4,4,5,6,7,8)</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>VZXTWGWHSMCWGA-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:0x00007f7226d0c088&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>10435</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>10005</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>
