<common-name>Tris[3-(heptafluoropropylhydroxymethylene)-(−)-camphorato]erbium</common-name> <description>Tris[3-(heptafluoropropylhydroxymethylene)-(−)-camphorato]erbium belongs to the monoterpenoids, a subclass of prenol lipids within the organic compounds. With an average molecular weight of 1,212 g/mol, Tris[3-(heptafluoropropylhydroxymethylene)-(−)-camphorato]erbium is a heavy molecule. This compound is characterized by the chemical formula C42H45ErF21O6. The substance is found in or released from thirteen recorded sources across several diverse sectors. Within Electrical & Electronic Equipment, it is associated with cell phones, capacitors, wires and cables, batteries, and printed circuit boards, among one other source. In the Textiles, leather & furnishings sector, it is found in carpets, rugs, and synthetic textiles. Other recorded sources include food packaging from the Food, food processing & cookware sector, medical devices from the Healthcare, pharmaceuticals & veterinary products sector, and lubricants used in both Energy, oil & gas as well as Industrial manufacturing & chemical processing. One additional sector is also recorded. Human exposure to the compound may occur through inhalation, oral intake, or touch.</description> <cas>123359-45-5</cas> <pubchem-id>71310122</pubchem-id> <chemical-formula>C42H45ErF21O6</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">2026-04-06T06:02:42Z</created-at> <updated-at type="dateTime">2026-05-21T05:11:11Z</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>[Er].CC1(C)[C@H]2CC[C@]1(C)C(=O)C2=C(/O)C(F)(F)C(F)(F)C(F)(F)F.CC1(C)[C@H]2CC[C@]1(C)C(=O)C2=C(/O)C(F)(F)C(F)(F)C(F)(F)F.CC1(C)[C@H]2CC[C@]1(C)C(=O)C2=C(O)C(F)(F)C(F)(F)C(F)(F)F</moldb-smiles> <moldb-formula>C42H45ErF21O6</moldb-formula> <moldb-inchi>InChI=1S/3C14H15F7O2.Er/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*6,23H,4-5H2,1-3H3;/b9-7+;2*9-7-;/t3*6-,11+;/m000./s1</moldb-inchi> <moldb-inchikey>VKBOLWUSVWLRDP-UFGMMYBOSA-N</moldb-inchikey> <moldb-average-mass type="decimal">1212.041</moldb-average-mass> <moldb-mono-mass type="decimal">1210.218375</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp nil="true"/> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id>57542757</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>CHEM118620</chemdb-id> <dsstox-id>DTXSID40746071</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00110237</susdat-id> <iupac>erbium;(1S,3E,4R)-3-(2,2,3,3,4,4,4-heptafluoro-1-hydroxybutylidene)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one;(1S,3Z,4R)-3-(2,2,3,3,4,4,4-heptafluoro-1-hydroxybutylidene)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one</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">0</paper-count> <sync-id>CED0120386</sync-id> <structure-inchikey>VKBOLWUSVWLRDP-KVWXVHIISA-N</structure-inchikey> <structure-fingerprint>100200000000003000000000010000080000000000000000000000000000040020000000000000008004000000200000000000000000000000000000000000000000400000000000000020000004000010000000000400000800000000010000000000000000000200000000020000000000000000001000100000000048000000000000000000000000200000000000000000000000000020000080000004000000000000080002000000000000040000000000000000000100000000000000000000000000000000000000000000000000000000000000000000000004000000000000000000000000800002000000000000000000000100</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle>ï¾Þ��F��H��€�D ��`�� `�� 4��`��`�� $��`��(��(��(��(��h�� `�� `�� 4��`��`�� $��`��(��(��(��(��h�� `�� `�� 4��`��`�� $��`��(��(��(��(��h�� (� � ��(�� !(� " "#(�#$ #%�%&�%'�%(�()�(*�(+�+,�+-�+.�/0�01�02�23�34�45�56�57�78(�79 9:(�:; :<�<=�<>�<?�?@�?A�?B�BC�BD�BE��50��"��92�B�� " ��02345�02975��</structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:45:57Z</structure-indexed-at> </compound>

122727 <common-name>Tris[3-(heptafluoropropylhydroxymethylene)-(−)-camphorato]erbium</common-name> <description>Tris[3-(heptafluoropropylhydroxymethylene)-(−)-camphorato]erbium belongs to the monoterpenoids, a subclass of prenol lipids within the organic compounds. With an average molecular weight of 1,212 g/mol, Tris[3-(heptafluoropropylhydroxymethylene)-(−)-camphorato]erbium is a heavy molecule. This compound is characterized by the chemical formula C42H45ErF21O6. The substance is found in or released from thirteen recorded sources across several diverse sectors. Within Electrical & Electronic Equipment, it is associated with cell phones, capacitors, wires and cables, batteries, and printed circuit boards, among one other source. In the Textiles, leather & furnishings sector, it is found in carpets, rugs, and synthetic textiles. Other recorded sources include food packaging from the Food, food processing & cookware sector, medical devices from the Healthcare, pharmaceuticals & veterinary products sector, and lubricants used in both Energy, oil & gas as well as Industrial manufacturing & chemical processing. One additional sector is also recorded. Human exposure to the compound may occur through inhalation, oral intake, or touch.</description> <cas>123359-45-5</cas> <pubchem-id>71310122</pubchem-id> <chemical-formula>C42H45ErF21O6</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">2026-04-06T06:02:42Z</created-at> <updated-at type="dateTime">2026-05-21T05:11:11Z</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>[Er].CC1(C)[C@H]2CC[C@]1(C)C(=O)C2=C(/O)C(F)(F)C(F)(F)C(F)(F)F.CC1(C)[C@H]2CC[C@]1(C)C(=O)C2=C(/O)C(F)(F)C(F)(F)C(F)(F)F.CC1(C)[C@H]2CC[C@]1(C)C(=O)C2=C(O)C(F)(F)C(F)(F)C(F)(F)F</moldb-smiles> <moldb-formula>C42H45ErF21O6</moldb-formula> <moldb-inchi>InChI=1S/3C14H15F7O2.Er/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*6,23H,4-5H2,1-3H3;/b9-7+;2*9-7-;/t3*6-,11+;/m000./s1</moldb-inchi> <moldb-inchikey>VKBOLWUSVWLRDP-UFGMMYBOSA-N</moldb-inchikey> <moldb-average-mass type="decimal">1212.041</moldb-average-mass> <moldb-mono-mass type="decimal">1210.218375</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp nil="true"/> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id>57542757</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>CHEM118620</chemdb-id> <dsstox-id>DTXSID40746071</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00110237</susdat-id> <iupac>erbium;(1S,3E,4R)-3-(2,2,3,3,4,4,4-heptafluoro-1-hydroxybutylidene)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one;(1S,3Z,4R)-3-(2,2,3,3,4,4,4-heptafluoro-1-hydroxybutylidene)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one</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">0</paper-count> <sync-id>CED0120386</sync-id> <structure-inchikey>VKBOLWUSVWLRDP-KVWXVHIISA-N</structure-inchikey> <structure-fingerprint>100200000000003000000000010000080000000000000000000000000000040020000000000000008004000000200000000000000000000000000000000000000000400000000000000020000004000010000000000400000800000000010000000000000000000200000000020000000000000000001000100000000048000000000000000000000000200000000000000000000000000020000080000004000000000000080002000000000000040000000000000000000100000000000000000000000000000000000000000000000000000000000000000000000004000000000000000000000000800002000000000000000000000100</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle>ï¾Þ��F��H��€�D ��`�� `�� 4��`��`�� $��`��(��(��(��(��h�� `�� `�� 4��`��`�� $��`��(��(��(��(��h�� `�� `�� 4��`��`�� $��`��(��(��(��(��h�� (� � ��(�� !(� " "#(�#$ #%�%&�%'�%(�()�(*�(+�+,�+-�+.�/0�01�02�23�34�45�56�57�78(�79 9:(�:; :<�<=�<>�<?�?@�?A�?B�BC�BD�BE��50��"��92�B�� " ��02345�02975��</structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:45:57Z</structure-indexed-at> </compound>