123325 <common-name>2,3,4,5,5,5-Hexafluoro-2,3,4-tris(trifluoromethyl)pentanoic acid</common-name> <description>2,3,4,5,5,5-Hexafluoro-2,3,4-tris(trifluoromethyl)pentanoic acid is an organic compound with the chemical formula C8HF15O2 and an average molecular weight of 414.07 g/mol. 2,3,4,5,5,5-Hexafluoro-2,3,4-tris(trifluoromethyl)pentanoic acid belongs to the fatty acids and conjugates, a subclass of fatty acyls within the organic compounds. This substance is found in or released from 13 recorded sources across multiple sectors. Within electrical and electronic equipment, it is associated with cell phones, capacitors, wires and cables, batteries, and printed circuit boards, among one other source. It is present in textiles, leather and furnishings, specifically within carpets, rugs, and synthetic textiles. In the healthcare, pharmaceuticals and veterinary products sector, it is linked to medical devices, while in food, food processing and cookware, it is found in food packaging. Additionally, the compound is utilized as lubricants in both industrial manufacturing and chemical processing as well as in the energy, oil and gas sectors. One other sector is also recorded as a source. Human exposure to the compound occurs through recorded routes of inhalation, oral ingestion, and touch.</description> <cas>1882109-72-9</cas> <pubchem-id>138396459</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">2026-04-06T06:42:20Z</created-at> <updated-at type="dateTime">2026-08-25T06:31:12Z</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)(C(F)(F)F)C(F)(C(F)(F)F)C(F)(C(F)(F)F)C(F)(F)F</moldb-smiles> <moldb-formula>C8HF15O2</moldb-formula> <moldb-inchi>InChI=1/C8HF15O2/c9-2(1(24)25,5(12,13)14)3(10,6(15,16)17)4(11,7(18,19)20)8(21,22)23/h(H,24,25)</moldb-inchi> <moldb-inchikey>CSDNZCNEOLXCQF-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>4.9</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>CHEM119218</chemdb-id> <dsstox-id>DTXSID60896582</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00111142</susdat-id> <iupac>2,3,4,5,5,5-Hexafluoro-2,3,4-tris(trifluoromethyl)pentanoic 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>CED0067426</sync-id> <structure-inchikey>CSDNZCNEOLXCQF-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>100000000000002000000000000000000000000000000000000000000000000000000000000040000004000000000000000000000000000000000000000000000000000000000000000020000000000000000000000000000000000000010000000000000000000200000000000000100000000000000000000000000000000800000000000000000000000000000000000000000000000000000000000008000000000000000000000000000000040000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000040000000400800040000000420000000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle type="binary" encoding="base64">776t3gAAAAAQAAAAAwAAAAAAAAAZAAAAGAAAAIABCABoAAAAAwEBBgAoAAAA AwQIACgAAAADAgYAIAAAAAQJACAAAAABBgAgAAAABAkAIAAAAAEJACAAAAAB CQAgAAAAAQYAIAAAAAQJACAAAAABBgAgAAAABAkAIAAAAAEJACAAAAABCQAg AAAAAQYAIAAAAAQJACAAAAABBgAgAAAABAkAIAAAAAEJACAAAAABCQAgAAAA AQYAIAAAAAQJACAAAAABCQAgAAAAAQkAIAAAAAELAAEgAQIoAgEDAAMEAAMF AAUGAAUHAAUIAAMJAAkKAAkLAAsMAAsNAAsOAAkPAA8QAA8RABESABETABEU AA8VABUWABUXABUYAEIAAAAAFwQAAAAAAAAAFg== </structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:46:32Z</structure-indexed-at> </compound>