<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">3908</id>
  <title>T3D3853</title>
  <common-name>Folpet</common-name>
  <description>Folpet is a protective leaf-fungicide. Its mode of action inhibits normal cell division of a broad spectrum of microorganisms. It is used to control cherry leaf spot, rose mildew, rose black spot, and apple scab. Used on berries, flowers, ornamentals, fruits and vegetables, and for seed- and plant-bed treatment. Also used as a fungicide in paints and plastics, and for treatment of internal and external structural surfaces of buildings. Folpet has low acute toxicity to mammals. It is slighly toxic to birds and bees, and is moderately toxic to fish, aquatic invertebrates, algae and earthworms. Folpet is very irritating to the eyes and repeated or prolonged contact leads to skin sensitization. Chronic exposure tests showed folpet to be carcinogenic in mice (but not rats). On this basis, folpet is considered possibly carcinogenic to humans.</description>
  <cas>133-07-3</cas>
  <pubchem-id>8607</pubchem-id>
  <chemical-formula>C9H4Cl3NO2S</chemical-formula>
  <weight nil="true"/>
  <appearance>White powder.</appearance>
  <melting-point>177°C</melting-point>
  <boiling-point nil="true"/>
  <density nil="true"/>
  <solubility>0.0008 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>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">2013-04-25T07:56:52Z</created-at>
  <updated-at type="dateTime">2026-03-27T00:23:01Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia nil="true"/>
  <uniprot-id nil="true"/>
  <kegg-compound-id>C18860</kegg-compound-id>
  <omim-id nil="true"/>
  <chebi-id>82019</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>ClC(Cl)(Cl)SN1C(=O)C2=CC=CC=C2C1=O</moldb-smiles>
  <moldb-formula>C9H4Cl3NO2S</moldb-formula>
  <moldb-inchi>InChI=1S/C9H4Cl3NO2S/c10-9(11,12)16-13-7(14)5-3-1-2-4-6(5)8(13)15/h1-4H</moldb-inchi>
  <moldb-inchikey>HKIOYBQGHSTUDB-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">296.558</moldb-average-mass>
  <moldb-mono-mass type="decimal">294.902832188</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Solid</state>
  <logp>2.85</logp>
  <hmdb-id>HMDB31792</hmdb-id>
  <chembl-id>CHEMBL1883819</chembl-id>
  <chemspider-id>8288</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>CHEM002814</chemdb-id>
  <dsstox-id>DTXSID0021385</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00005935</susdat-id>
  <iupac>2-[(trichloromethyl)sulfanyl]-2,3-dihydro-1H-isoindole-1,3-dione</iupac>
</compound>
