108105 <common-name>N:2 fluorotelomer thio alkyl amido sulfonic acids, n=7</common-name> <description>N:2 fluorotelomer thio alkyl amido sulfonic acids, n=7 belongs to the organosulfonic acids and derivatives, a subclass of organic sulfonic acids and derivatives within the organic compounds. This compound has the chemical formula C23H18F29NO4S2. With an average molecular weight of 987.47 g/mol, N:2 fluorotelomer thio alkyl amido sulfonic acids, n=7 is a heavy molecule. The compound is associated with 13 recorded sources across several sectors. Within the Electrical & Electronic Equipment sector, it is found in or released from batteries, capacitors, printed circuit boards, wires and cables, cell phones, and one additional source. In the Textiles, leather & furnishings sector, it is linked to carpets, rugs, and synthetic textiles. Other sources include food packaging from the Food, food processing & cookware sector, medical devices from the Healthcare, pharmaceuticals & veterinary products sector, and lubricants from both the Energy, oil & gas and Industrial manufacturing & chemical processing sectors, along with one further sector. Recorded exposure routes for this substance include oral, inhalation, and touch.</description> <cas>1513864-08-8</cas> <pubchem-id>138394474</pubchem-id> <chemical-formula>C23H18F29NO4S2</chemical-formula> <weight>987.5</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">2026-04-05T14:55:35Z</created-at> <updated-at type="dateTime">2026-08-30T16:09:54Z</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>CC(C)(CS(O)(=O)=O)NC(=O)CCSCCC(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)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F</moldb-smiles> <moldb-formula>C23H18F29NO4S2</moldb-formula> <moldb-inchi>InChI=1S/C23H18F29NO4S2/c1-9(2,7-59(55,56)57)53-8(54)3-5-58-6-4-10(24,25)11(26,27)12(28,29)13(30,31)14(32,33)15(34,35)16(36,37)17(38,39)18(40,41)19(42,43)20(44,45)21(46,47)22(48,49)23(50,51)52/h3-7H2,1-2H3,(H,53,54)(H,55,56,57)</moldb-inchi> <moldb-inchikey>OETXJTOSJNJQGJ-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">987.47</moldb-average-mass> <moldb-mono-mass type="decimal">987.0214184</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>9.8</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>CHEM103998</chemdb-id> <dsstox-id>DTXSID70893047</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00074863</susdat-id> <iupac>2-methyl-2-[3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15,16,16,16-nonacosafluorohexadecylsulfanyl)propanoylamino]propane-1-sulfonic 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>Organic acids and derivatives</superklass> <klass>Organic sulfonic acids and derivatives</klass> <subklass>Organosulfonic acids and derivatives</subklass> <paper-count type="integer">2</paper-count> <sync-id>CED0051837</sync-id> <structure-inchikey>OETXJTOSJNJQGJ-UHFFFAOYSA-N</structure-inchikey> 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