122915 <common-name>3-(Perfluorooctyl)-2-hydroxypropyl acrylate</common-name> <description>3-(Perfluorooctyl)-2-hydroxypropyl acrylate belongs to the acrylic acids and derivatives, a subclass of carboxylic acids and derivatives within the organic compounds. With an average molecular weight of 548.20 g/mol, 3-(Perfluorooctyl)-2-hydroxypropyl acrylate is a heavy molecule. It has the chemical formula C14H9F17O3. This compound is found in or released from 13 recorded sources across multiple sectors. Within 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. In the textiles, leather and furnishings sector, it is linked to carpets, rugs, and synthetic textiles. Other recorded sources include medical devices from the healthcare, pharmaceuticals and veterinary products sector, food packaging from the food, food processing and cookware sector, and lubricants from both the energy, oil and gas sector as well as the industrial manufacturing and chemical processing sector. Additionally, it is found in one more sector. Recorded exposure routes for this compound include inhalation, oral, and touch.</description> <cas>76962-34-0</cas> <pubchem-id>2776307</pubchem-id> <chemical-formula>C14H9F17O3</chemical-formula> <weight>548.19</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">2026-04-06T06:17:44Z</created-at> <updated-at type="dateTime">2026-08-19T08:32:42Z</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(COC(=O)C=C)CC(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>C14H9F17O3</moldb-formula> <moldb-inchi>InChI=1S/C14H9F17O3/c1-2-6(33)34-4-5(32)3-7(15,16)8(17,18)9(19,20)10(21,22)11(23,24)12(25,26)13(27,28)14(29,30)31/h2,5,32H,1,3-4H2</moldb-inchi> <moldb-inchikey>DAEIFBGPFDVHNR-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">548.196</moldb-average-mass> <moldb-mono-mass type="decimal">548.0280239</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>6.3</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>CHEM118808</chemdb-id> <dsstox-id>DTXSID50379975</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00110537</susdat-id> <iupac>4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-Heptadecafluoro-2-hydroxyundecyl prop-2-enoate</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>Acrylic acids and derivatives</subklass> <paper-count type="integer">0</paper-count> <sync-id>CED0088161</sync-id> <structure-inchikey>DAEIFBGPFDVHNR-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>40000000000000100000800000002200000010000000000000000000100000000000000000000000000000000000000000000000000000000000000000000804001000000000000000000000000000000020000000000300000000000000000000000000010000400000000000000200000008000000000100080000000000000000008800004000000000000000000000000000000000000000000000010000000000000000020000000200000002000000000000040000000000000000000000000000000000000000000000040000000000000000000000000000000000000020000000000000000100000000000400800000000000000000000000000200</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle>ï¾­Þ����������������"���!���€���`�������`�������`�������(�������(�������(�������h��������h��������`������� ���� � ���� � ������ ���� � ���� � ������ ���� � ���� � ������ ���� � ���� � ������ ���� � ���� � ������ ���� � ���� � ������ ���� � ���� � ������ ���� � ���� � ���� � ���������������� ��(��� ��(����� � � �� ��� �������������������������������������������������������� ��!�B��������������</structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:46:10Z</structure-indexed-at> </compound>