<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">122162</id>
  <title nil="true"/>
  <common-name>2,3,3,3-Tetrafluoro-2-(trifluoromethyl)propan-1-amine</common-name>
  <description>2,3,3,3-Tetrafluoro-2-(trifluoromethyl)propan-1-amine belongs to the organofluorides, a class of organohalogen compounds within the organic compounds. This compound has the chemical formula C4H4F7N and an average molecular weight of 199.07 g/mol.

The substance is found in or released from 13 recorded sources across several sectors. Within electrical and electronic equipment, it is associated with capacitors, batteries, cell phones, printed circuit boards, wires and cables, and one additional source. In the textiles, leather and furnishings sector, it is linked to carpets, rugs, and synthetic textiles. Other sources include food packaging from the food, food processing and cookware sector, and medical devices from the healthcare, pharmaceuticals and veterinary products sector. Additionally, it is found in lubricants within both the energy, oil and gas sector and the industrial manufacturing and chemical processing sector, as well as one other sector. Recorded exposure routes for this compound include oral, inhalation, and touch.</description>
  <cas>182243-54-5</cas>
  <pubchem-id>125424351</pubchem-id>
  <chemical-formula>C4H4F7N</chemical-formula>
  <weight>199.07</weight>
  <appearance nil="true"/>
  <melting-point nil="true"/>
  <boiling-point nil="true"/>
  <density nil="true"/>
  <solubility nil="true"/>
  <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 nil="true"/>
  <use-source nil="true"/>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms nil="true"/>
  <treatment nil="true"/>
  <created-at type="dateTime">2026-04-06T05:24:36Z</created-at>
  <updated-at type="dateTime">2026-08-22T16:48:37Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia nil="true"/>
  <uniprot-id nil="true"/>
  <kegg-compound-id nil="true"/>
  <omim-id nil="true"/>
  <chebi-id nil="true"/>
  <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>NCC(F)(C(F)(F)F)C(F)(F)F</moldb-smiles>
  <moldb-formula>C4H4F7N</moldb-formula>
  <moldb-inchi>InChI=1S/C4H4F7N/c5-2(1-12,3(6,7)8)4(9,10)11/h1,12H2</moldb-inchi>
  <moldb-inchikey>WRAHZJQESWMXQC-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">199.072</moldb-average-mass>
  <moldb-mono-mass type="decimal">199.0231967</moldb-mono-mass>
  <origin nil="true"/>
  <state nil="true"/>
  <logp>1.7</logp>
  <hmdb-id nil="true"/>
  <chembl-id nil="true"/>
  <chemspider-id nil="true"/>
  <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>CHEM118055</chemdb-id>
  <dsstox-id>DTXSID10896294</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00109407</susdat-id>
  <iupac>2,3,3,3-Tetrafluoro-2-(trifluoromethyl)propan-1-amine</iupac>
  <moldb-polar-surface-area nil="true"/>
  <moldb-refractivity nil="true"/>
  <moldb-polarizability nil="true"/>
  <moldb-rotatable-bond-count nil="true"/>
  <moldb-acceptor-count nil="true"/>
  <moldb-donor-count nil="true"/>
  <moldb-pka-strongest-acidic nil="true"/>
  <moldb-pka-strongest-basic nil="true"/>
  <moldb-physiological-charge nil="true"/>
  <moldb-number-of-rings nil="true"/>
  <moldb-alogps-logp nil="true"/>
  <moldb-alogps-logs nil="true"/>
  <moldb-alogps-solubility nil="true"/>
  <kingdom>Organic compounds</kingdom>
  <superklass>Organohalogen compounds</superklass>
  <klass>Organofluorides</klass>
  <subklass nil="true"/>
  <paper-count type="integer">0</paper-count>
  <sync-id>CED0095284</sync-id>
  <structure-inchikey>WRAHZJQESWMXQC-UHFFFAOYSA-N</structure-inchikey>
  <structure-fingerprint>100000800000002000000000000000000000000000000000000000000000000000000000000000000000000000000004000000000000000000000000000000000000000000000000000000000000000000100000000100000000000000000000000000000000000000000000000000000000000400000000000000000000000000000000000000000000001000000000000000000000000000000000000000000000000000000000000000000000040000000000000000000001000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000800000000000000000000000200000</structure-fingerprint>
  <structure-pattern-fingerprint>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</structure-pattern-fingerprint>
  <structure-pickle>ï¾­Þ������������������������€���`�������`������� ����	� ������ ����	� ����	� ����	� ������ ����	� ����	� ����	� ������������������������������	��
����B��������������</structure-pickle>
  <structure-indexed-at type="dateTime">2026-09-19T04:45:25Z</structure-indexed-at>
</compound>
