66146 <common-name>Bis-(1H,1H,7H-perfluoroheptyl) (1S,3R)-camphorate</common-name> <description>Bis-(1H,1H,7H-perfluoroheptyl) (1S,3R)-camphorate belongs to the dicarboxylic acids and derivatives, a subclass of carboxylic acids and derivatives within the organic compounds. This compound has the chemical formula C24H20F24O4. With an average molecular weight of 828.38 g/mol, Bis-(1H,1H,7H-perfluoroheptyl) (1S,3R)-camphorate is a heavy molecule. The compound is found in or released from 13 recorded sources across several sectors. Within electrical and electronic equipment, it is associated with capacitors, cell phones, batteries, printed circuit boards, wires and cables, and one additional source. It is also found in food packaging under the food, food processing and cookware sector, and in medical devices within healthcare, pharmaceuticals and veterinary products. In the textiles, leather and furnishings sector, it is linked to carpets, rugs, and synthetic textiles. Furthermore, it is used as lubricants in both industrial manufacturing and chemical processing as well as in the energy, oil and gas sectors. One additional sector is also recorded. Recorded exposure routes for this substance include inhalation, oral, and touch.</description> <cas nil="true"/> <pubchem-id>2736060</pubchem-id> <chemical-formula>C24H20F24O4</chemical-formula> <weight>828.4</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">2026-04-03T05:28:58Z</created-at> <updated-at type="dateTime">2026-08-22T02:47:59Z</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>CC1(C)[C@@H](CC[C@]1(C)C(=O)OCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)F)C(=O)OCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)F</moldb-smiles> <moldb-formula>C24H20F24O4</moldb-formula> <moldb-inchi>InChI=1S/C24H20F24O4/c1-13(2)8(9(49)51-6-15(29,30)19(37,38)23(45,46)21(41,42)17(33,34)10(25)26)4-5-14(13,3)12(50)52-7-16(31,32)20(39,40)24(47,48)22(43,44)18(35,36)11(27)28/h8,10-11H,4-7H2,1-3H3</moldb-inchi> <moldb-inchikey>VPEPXOMYWDUPOA-RMLUDKJBSA-N</moldb-inchikey> <moldb-average-mass type="decimal">828.382</moldb-average-mass> <moldb-mono-mass type="decimal">828.097836</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>10.4</logp> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id>16737179</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>CHEM062039</chemdb-id> <dsstox-id>DTXSID80880180</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00018864</susdat-id> <iupac>bis(2,2,3,3,4,4,5,5,6,6,7,7-dodecafluoroheptyl) (1S,3R)-1,2,2-trimethylcyclopentane-1,3-dicarboxylate</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>Dicarboxylic acids and derivatives</subklass> <paper-count type="integer">0</paper-count> <sync-id>CED0117595</sync-id> <structure-inchikey>VPEPXOMYWDUPOA-RMLUDKJBSA-N</structure-inchikey> 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