123324 <common-name>2,2,4,4,5,5,6,6,6-Nonafluoro-3,3-bis(trifluoromethyl)hexanoic acid</common-name> <description>2,2,4,4,5,5,6,6,6-Nonafluoro-3,3-bis(trifluoromethyl)hexanoic acid belongs to the fatty acids and conjugates, a subclass of fatty acyls within the organic compounds. This compound has the chemical formula C8HF15O2 and an average molecular weight of 414.07 g/mol. The compound is found in or released from 13 recorded sources across several sectors. In the electrical and electronic equipment sector, it is associated with capacitors, cell phones, printed circuit boards, batteries, wires and cables, and one additional source. Within the textiles, leather and furnishings sector, it is found in synthetic textiles as well as carpets and rugs. It is also present in food packaging within the food, food processing and cookware sector, and in medical devices within the healthcare, pharmaceuticals and veterinary products sector. Additionally, it is used as a lubricant in both the energy, oil and gas sector and the industrial manufacturing and chemical processing sector, with one other sector also recorded. Recorded exposure routes for this substance include inhalation, oral, and touch.</description> <cas>1812247-20-3</cas> <pubchem-id>138396445</pubchem-id> <chemical-formula>C8HF15O2</chemical-formula> <weight>414.07</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">2026-04-06T06:42:18Z</created-at> <updated-at type="dateTime">2026-08-25T06:31:51Z</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>OC(=O)C(F)(F)C(C(F)(F)F)(C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)F</moldb-smiles> <moldb-formula>C8HF15O2</moldb-formula> <moldb-inchi>InChI=1S/C8HF15O2/c9-2(10,1(24)25)3(6(15,16)17,7(18,19)20)4(11,12)5(13,14)8(21,22)23/h(H,24,25)</moldb-inchi> <moldb-inchikey>QTNXQUUMDZPDRJ-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">414.07</moldb-average-mass> <moldb-mono-mass type="decimal">413.9737026</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>5.3</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>CHEM119217</chemdb-id> <dsstox-id>DTXSID60896567</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00111141</susdat-id> <iupac>2,2,4,4,5,5,6,6,6-Nonafluoro-3,3-bis(trifluoromethyl)hexanoic acid</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>Lipids and lipid-like molecules</superklass> <klass>Fatty Acyls</klass> <subklass>Fatty acids and conjugates</subklass> <paper-count type="integer">1</paper-count> <sync-id>CED0067367</sync-id> <structure-inchikey>QTNXQUUMDZPDRJ-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>100000000000002000000000000000000000000000000000000000000000000000000000000000000004000000000000000000001000000000000000000000000000000000000000000020000008000000000000000000000000000000010000000000000000000200000008000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000020000000000000000000000000002000000000000040000000000000000000000000000000000004000000000000000000000000000000800000000000000000000020004000000000000000000000400800000000000400000000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle type="binary" encoding="base64">776t3gAAAAAQAAAAAwAAAAAAAAAZAAAAGAAAAIABCABoAAAAAwEBBgAoAAAA AwQIACgAAAADAgYAIAAAAAQJACAAAAABCQAgAAAAAQYAIAAAAAQGACAAAAAE CQAgAAAAAQkAIAAAAAEJACAAAAABBgAgAAAABAkAIAAAAAEJACAAAAABCQAg AAAAAQYAIAAAAAQJACAAAAABCQAgAAAAAQYAIAAAAAQJACAAAAABCQAgAAAA AQYAIAAAAAQJACAAAAABCQAgAAAAAQkAIAAAAAELAAEgAQIoAgEDAAMEAAMF AAMGAAYHAAcIAAcJAAcKAAYLAAsMAAsNAAsOAAYPAA8QAA8RAA8SABITABIU ABIVABUWABUXABUYAEIAAAAAFwQAAAAAAAAAFg== </structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:46:31Z</structure-indexed-at> </compound>