108118 <common-name>N:2 fluorotelomer sulfonyl propano-amido alkyl sulfonic acids, n=3</common-name> <description>N:2 fluorotelomer sulfonyl propano-amido alkyl sulfonic acids, n=3 belongs to the organosulfonic acids and derivatives, a subclass of organic sulfonic acids and derivatives within the organic compounds. With an average molecular weight of 619.41 g/mol, N:2 fluorotelomer sulfonyl propano-amido alkyl sulfonic acids, n=3 is a heavy molecule. Its chemical formula is C15H18F13NO6S2. This compound is found in or released from 13 recorded sources across several sectors. In the electrical and electronic equipment sector, it is associated with cell phones, capacitors, wires and cables, batteries, and printed circuit boards, among one other source. Within textiles, leather and furnishings, it is found in carpets, rugs, and synthetic textiles. Other recorded sources include food packaging from the food, food processing and cookware sector, as well as medical devices from the healthcare, pharmaceuticals and veterinary products sector. Additionally, the compound is identified in lubricants used in energy, oil and gas, as well as industrial manufacturing and chemical processing, along with one other sector. Recorded exposure routes for this substance include inhalation, oral, and touch.</description> <cas>1911606-13-7</cas> <pubchem-id>138394570</pubchem-id> <chemical-formula>C15H18F13NO6S2</chemical-formula> <weight>619.4</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">2026-04-05T14:56:43Z</created-at> <updated-at type="dateTime">2026-08-19T10:50:36Z</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)CCS(=O)(=O)CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F</moldb-smiles> <moldb-formula>C15H18F13NO6S2</moldb-formula> <moldb-inchi>InChI=1S/C15H18F13NO6S2/c1-9(2,7-37(33,34)35)29-8(30)3-5-36(31,32)6-4-10(16,17)11(18,19)12(20,21)13(22,23)14(24,25)15(26,27)28/h3-7H2,1-2H3,(H,29,30)(H,33,34,35)</moldb-inchi> <moldb-inchikey>RZBHYDQKJKDSNP-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">619.41</moldb-average-mass> <moldb-mono-mass type="decimal">619.0367962</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>3.2</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>CHEM104011</chemdb-id> <dsstox-id>DTXSID90894132</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00074895</susdat-id> <iupac>2-methyl-2-[3-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylsulfonyl)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">0</paper-count> <sync-id>CED0112201</sync-id> <structure-inchikey>RZBHYDQKJKDSNP-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>8000004000100000900000002000000000000000000000000000000000000000001000000000000000022000080000800040000000000000000040000000000000000000000000008000000001000020000000000000000001000000000000000000010000000000000100000201000808000000000000080000000000000000000840000000004000000400000080000200000000000000000000010000000000080000000000000000000002800000000000040000080000000000000000000008000000000000000000000000000000400000000000000000000000000000000000000000000000000000000400800000000000000000000000000000</structure-fingerprint> 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