<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">4591</id>
  <title>T3D4537</title>
  <common-name>Cyanuric acid</common-name>
  <description>Because of their trifunctionality, CYA is a precursor to crosslinking agents, especially for polyurethane resins. Cyanuric acid or 1,3,5-triazine-2,4,6-triol is a chemical compound with the formula (CNOH)3. Like many industrially useful chemicals, this triazine has many synonyms. This white, odorless solid finds use as a precursor or a component of bleaches, disinfectants, and herbicides. In 1997, worldwide production was 160 million kilograms.</description>
  <cas>108-80-5</cas>
  <pubchem-id>7956</pubchem-id>
  <chemical-formula>C3H3N3O3</chemical-formula>
  <weight>129.07</weight>
  <appearance>White powder.</appearance>
  <melting-point>360°C</melting-point>
  <boiling-point></boiling-point>
  <density nil="true"/>
  <solubility>2 mg/mL at 25°C</solubility>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure nil="true"/>
  <target nil="true"/>
  <mechanism-of-toxicity nil="true"/>
  <metabolism nil="true"/>
  <toxicity nil="true"/>
  <lethaldose nil="true"/>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>This is a man-made compound that is used as a pesticide.</use-source>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms nil="true"/>
  <treatment nil="true"/>
  <created-at type="dateTime">2014-08-29T06:51:46Z</created-at>
  <updated-at type="dateTime">2026-04-16T21:14:59Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>cyanuric_acid</wikipedia>
  <uniprot-id nil="true"/>
  <kegg-compound-id>C06554</kegg-compound-id>
  <omim-id nil="true"/>
  <chebi-id>17696</chebi-id>
  <biocyc-id nil="true"/>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id nil="true"/>
  <pdb-id nil="true"/>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>OC1=NC(O)=NC(O)=N1</moldb-smiles>
  <moldb-formula>C3H3N3O3</moldb-formula>
  <moldb-inchi>InChI=1S/C3H3N3O3/c7-1-4-2(8)6-3(9)5-1/h(H3,4,5,6,7,8,9)</moldb-inchi>
  <moldb-inchikey>ZFSLODLOARCGLH-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">129.0742</moldb-average-mass>
  <moldb-mono-mass type="decimal">129.017440977</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Solid</state>
  <logp nil="true"/>
  <hmdb-id>HMDB41861</hmdb-id>
  <chembl-id>CHEMBL1698868</chembl-id>
  <chemspider-id>7668</chemspider-id>
  <structure-image-file-name nil="true"/>
  <structure-image-content-type nil="true"/>
  <structure-image-file-size type="integer" nil="true"/>
  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference nil="true"/>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM003497</chemdb-id>
  <dsstox-id>DTXSID7024873</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00009566</susdat-id>
  <iupac>1,3,5-triazine-2,4,6-triol</iupac>
</compound>
