122210 <common-name>Europium tri[3-(heptafluoropropylhydroxymethylene)]-(+)-camphorate</common-name> <description>Europium tri[3-(heptafluoropropylhydroxymethylene)]-(+)-camphorate (C42H42EuF21O6) is a chemical compound found in or released from 13 recorded sources. These sources span multiple sectors, including electrical and electronic equipment such as cell phones, capacitors, wires and cables, batteries, and printed circuit boards. It is also present in textiles, leather and furnishings, specifically synthetic textiles and carpets and rugs. Additional sources include food packaging within the food, food processing and cookware sector, medical devices in healthcare, pharmaceuticals and veterinary products, and lubricants used in both energy, oil and gas as well as industrial manufacturing and chemical processing. Europium tri[3-(heptafluoropropylhydroxymethylene)]-(+)-camphorate belongs to the monoterpenoids, a subclass of prenol lipids within the organic compounds. With an average molecular weight of 1,194 g/mol, Europium tri[3-(heptafluoropropylhydroxymethylene)]-(+)-camphorate is a heavy molecule. Recorded exposure routes for this substance include inhalation, oral, and touch.</description> <cas>34788-82-4</cas> <pubchem-id>481142871</pubchem-id> <chemical-formula>C42H42EuF21O6</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">2026-04-06T05:26:57Z</created-at> <updated-at type="dateTime">2026-05-21T03:44:05Z</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>[Eu+3].CC1(C)C2CCC1(C)C(=O)[C-]2C(=O)C(F)(F)C(F)(F)C(F)(F)F.CC1(C)C2CCC1(C)C(=O)[C-]2C(=O)C(F)(F)C(F)(F)C(F)(F)F.CC1(C)C2CCC1(C)C(=O)[C-]2C(=O)C(F)(F)C(F)(F)C(F)(F)F</moldb-smiles> <moldb-formula>C42H42EuF21O6</moldb-formula> <moldb-inchi>InChI=1S/3C14H14F7O2.Eu/c3*1-10(2)6-4-5-11(10,3)8(22)7(6)9(23)12(15,16)13(17,18)14(19,20)21;/h3*6H,4-5H2,1-3H3;/q3*-1;+3</moldb-inchi> <moldb-inchikey>ODBVBAQADHJDQG-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">1193.722</moldb-average-mass> <moldb-mono-mass type="decimal">1194.185837</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp nil="true"/> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id>2006132</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>CHEM118103</chemdb-id> <dsstox-id>DTXSID10897307</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00109462</susdat-id> <iupac>Europium(3+) tris[2-(2,2,3,3,4,4,4-heptafluorobutanoyl)-4,7,7-trimethyl-3-oxobicyclo[2.2.1]heptan-2-ide]</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>Lipids and lipid-like molecules</superklass> <klass>Prenol lipids</klass> <subklass>Monoterpenoids</subklass> <paper-count type="integer">4</paper-count> <sync-id>CED0044284</sync-id> <structure-inchikey>ODBVBAQADHJDQG-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>100020000000012000000000000000080000000000000000000000000000000020000000000000000000000000200000000000000000000000000000000000000000000000000000000030000000000000000001000400000800000000010000000400000000000200000000060800000000000000000040100000000048000000000000000000000000200000000000000000000000000020200000000004000000000000080002000000000000040000000000000000000000000000000000000040000000000000000000000000040000000000000000000000040004000000004000000000000400800000000000000000001000000000</structure-fingerprint> 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