132222 <common-name>1H,1H,2H,2H-perfluorododecyl acetate</common-name> <description>1H,1H,2H,2H-perfluorododecyl acetate belongs to the carboxylic acid derivatives, a subclass of carboxylic acids and derivatives within the organic compounds. It has the formula C14H7F21O2. With an average molecular weight of 606.17 g/mol, 1H,1H,2H,2H-perfluorododecyl acetate is a heavy molecule.</description> <cas>37858-05-2</cas> <pubchem-id>138395138</pubchem-id> <chemical-formula>C14H7F21O2</chemical-formula> <weight nil="true"/> <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">2026-04-06T17:10:26Z</created-at> <updated-at type="dateTime">2026-04-06T17:10:26Z</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(=O)OCCC(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>C14H7F21O2</moldb-formula> <moldb-inchi>InChI=1S/C14H7F21O2/c1-4(36)37-3-2-5(15,16)6(17,18)7(19,20)8(21,22)9(23,24)10(25,26)11(27,28)12(29,30)13(31,32)14(33,34)35/h2-3H2,1H3</moldb-inchi> <moldb-inchikey>OPXUYFLZHIENEF-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">606.174</moldb-average-mass> <moldb-mono-mass type="decimal">606.0110709</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp nil="true"/> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id>95729835</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>CHEM128115</chemdb-id> <dsstox-id>DTXSID101009907</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00134714</susdat-id> <iupac>3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12-Henicosafluorododecyl acetate</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>Carboxylic acid derivatives</subklass> <paper-count type="integer">9</paper-count> <sync-id>CED0036414</sync-id> <structure-inchikey>OPXUYFLZHIENEF-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>40000000000100000800000002000000010002000000000000000000000000000000000000080000000000000000000000000000000000000000000000000000000000000000000000008000000000020000000000100000000000000000000000000010000000002000000000200000008000000000000080000000000400010000840000000000000000000000000000200000000000000000000010000000000080000000000000000000002000000000000040000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000400800000000000000000000000000000</structure-fingerprint> 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