108134 <common-name>N:1:2 fluorotelomer betaine-related, n=3</common-name> <description>N:1:2 fluorotelomer betaine-related, n=3 belongs to the amino acids, peptides, and analogues, a subclass of carboxylic acids and derivatives within the organic compounds. With an average molecular weight of 532.24 g/mol, N:1:2 fluorotelomer betaine-related, n=3 is a heavy molecule. Its chemical formula is C14H14F16NO2. This compound has been identified in or released from 13 recorded sources across several sectors. Within the Electrical & Electronic Equipment sector, it is associated with cell phones, capacitors, wires and cables, batteries, and printed circuit boards, among one other source. It is found in the Textiles, leather & furnishings sector in synthetic textiles as well as carpets and rugs. Other identified 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. Additionally, it has been recorded in one other sector. Human exposure to N:1:2 fluorotelomer betaine-related, n=3 occurs through inhalation, oral, and touch routes.</description> <cas nil="true"/> <pubchem-id>138394376</pubchem-id> <chemical-formula>C14H14F16NO2</chemical-formula> <weight>532.24</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">2026-04-05T14:57:52Z</created-at> <updated-at type="dateTime">2026-08-28T05:13:57Z</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>C[N+](C)(CCC(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)F)CC(=O)O</moldb-smiles> <moldb-formula>C14H14F16NO2</moldb-formula> <moldb-inchi>InChI=1S/C14H13F16NO2/c1-31(2,5-7(32)33)4-3-6(15)8(16,17)9(18,19)10(20,21)11(22,23)12(24,25)13(26,27)14(28,29)30/h6H,3-5H2,1-2H3/p+1</moldb-inchi> <moldb-inchikey>DYECIQLCZJYVHI-UHFFFAOYSA-O</moldb-inchikey> <moldb-average-mass type="decimal" nil="true"/> <moldb-mono-mass type="decimal">532.0769052</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>5.8</logp> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id>95787042</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>CHEM104027</chemdb-id> <dsstox-id nil="true"/> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00074923</susdat-id> <iupac>carboxymethyl-(3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-hexadecafluorodecyl)-dimethylazanium</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>Carboxylic acids and derivatives</klass> <subklass>Amino acids, peptides, and analogues</subklass> <paper-count type="integer">0</paper-count> <sync-id>CED0119826</sync-id> <structure-inchikey>DYECIQLCZJYVHI-UHFFFAOYSA-O</structure-inchikey> <structure-fingerprint>40000000000000100000800000002000800000000000000000000000000000000000000000000000000008000000000004000002000000000000000000000000000000000000004000000000000008000020000000000000000000001000000000010000010000010000000400000200000048000000000000080000000000000000002040000000000000000000000000000000000000000000000000000000000000000000000000000000000002200001000000040000000000000000000000000000000020004000000000000000000000000000000000400000001000000000000000000000000000000000000400800000000000000000000000000400</structure-fingerprint> 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