108075 <common-name>9:2 Fluorotelomer carboxylic acid</common-name> <description>9:2 Fluorotelomer carboxylic acid belongs to the fatty acids and conjugates, a subclass of fatty acyls within the organic compounds. With an average molecular weight of 528.11 g/mol, 9:2 Fluorotelomer carboxylic acid is a heavy molecule. It is characterized by the chemical formula C11H3F19O2. This compound is found in or released from 13 recorded sources across multiple sectors. Within Electrical & 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 & furnishings, specifically in carpets, rugs, and synthetic textiles. Other sources include food packaging from the food, food processing & cookware sector, as well as medical devices from the healthcare, pharmaceuticals & veterinary products sector. Additionally, it is found in lubricants used in both energy, oil & gas as well as industrial manufacturing & chemical processing, along with one more sector. Recorded exposure routes for this substance include inhalation, oral, and touch.</description> <cas>191852-87-6</cas> <pubchem-id>10864353</pubchem-id> <chemical-formula>C11H3F19O2</chemical-formula> <weight>528.11</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">2026-04-05T14:53:27Z</created-at> <updated-at type="dateTime">2026-08-27T18:09:16Z</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)CC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F</moldb-smiles> <moldb-formula>C11H3F19O2</moldb-formula> <moldb-inchi>InChI=1S/C11H3F19O2/c12-3(13,1-2(31)32)4(14,15)5(16,17)6(18,19)7(20,21)8(22,23)9(24,25)10(26,27)11(28,29)30/h1H2,(H,31,32)</moldb-inchi> <moldb-inchikey>HIVKFEZPOKLBMW-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">528.113</moldb-average-mass> <moldb-mono-mass type="decimal">527.9829655</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>6.2</logp> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id>9039640</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>CHEM103968</chemdb-id> <dsstox-id>DTXSID601033088</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00074826</susdat-id> <iupac>3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-nonadecafluoroundecanoic 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">203</paper-count> <sync-id>CED0015182</sync-id> <structure-inchikey>HIVKFEZPOKLBMW-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>100000800000002000000000000000000000000000000000000000000000000000000000000000000004000000000000000000000000000000000000000000000000000000000000200020000000000000000000000000000000000000010000000000000000000200000008000000000000080000000000000000000804000000000000000000000000000000000000000000000000010000000000000000000000000000000002000000000000040000000000000000000000000000000000000000000000000000000000000000000000400000000000000000800000000000000008000000000400800000000000000000000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle>ï¾­Þ���������������� �������€���h��������(�������(�������`������� ���� � ���� � ������ ���� � ���� � ������ ���� � ���� � ������ ���� � ���� � ������ ���� � ���� � ������ ���� � ���� � ������ ���� � ���� � ������ ���� � ���� � ������ ���� � ���� � ���� � ������� ��(�������������������� �� � �� �� � �� �� �����������������������������������������������B��������������</structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:42:44Z</structure-indexed-at> </compound>