<common-name>Allyltris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)stannane</common-name> <description>Allyltris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)stannane belongs to the organotin compounds, a subclass of organo-post-transition metal compounds within the organic compounds. With an average molecular weight of 1,201 g/mol, Allyltris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)stannane is a heavy molecule. It is characterized by the chemical formula C27H17F39Sn. The compound is found in or released from 13 recorded sources across several sectors. In electrical and electronic equipment, it is associated with cell phones, capacitors, wires and cables, batteries, and printed circuit boards, among one other source. Within the textiles, leather and furnishings sector, it is found in carpets, rugs, and synthetic textiles. It is also present in food packaging within the food, food processing and cookware sector, and in medical devices within the healthcare, pharmaceuticals and veterinary products sector. Additionally, the compound is used as lubricants in both the energy, oil and gas sector and the industrial manufacturing and chemical processing sector, as well as in one other sector. Recorded routes of exposure for this substance include inhalation, oral ingestion, and touch.</description> <cas>192212-66-1</cas> <pubchem-id>10510526</pubchem-id> <chemical-formula>C27H17F39Sn</chemical-formula> <weight>1201.1</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">2026-04-06T06:01:16Z</created-at> <updated-at type="dateTime">2026-08-17T20:46:59Z</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>FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)CC[Sn](CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)(CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)CC=C</moldb-smiles> <moldb-formula>C27H17F39Sn</moldb-formula> <moldb-inchi>InChI=1S/3C8H4F13.C3H5.Sn/c3*1-2-3(9,10)4(11,12)5(13,14)6(15,16)7(17,18)8(19,20)21;1-3-2;/h3*1-2H2;3H,1-2H2;</moldb-inchi> <moldb-inchikey>RMDIHFFKXXTNGQ-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">1201.081</moldb-average-mass> <moldb-mono-mass type="decimal">1201.972951</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp nil="true"/> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id>8685927</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>CHEM118596</chemdb-id> <dsstox-id>DTXSID40440946</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00110212</susdat-id> <iupac>(Prop-2-en-1-yl)tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)stannane</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>Organometallic compounds</superklass> <klass>Organo-post-transition metal compounds</klass> <subklass>Organotin compounds</subklass> <paper-count type="integer">0</paper-count> <sync-id>CED0108997</sync-id> <structure-inchikey>RMDIHFFKXXTNGQ-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>100000800000002000000000000000000000000000000000000000000000000000000000000000000000000000000002000000000000000020000000000000000000000000000000000000008000000200000000000000000000000000000000000000000800000200000008000008000000080000000000000000000800000000000000000000000000000200080000080000000000010080000000080000000000000200000002000000000000040000000000000000000000002000000000000000000000040000000000000000000000000000000000000000000000000000000000000000000000800004000000000000000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle>ï¾Þ��C��B��€� � �� `��`��2 ��`��`�� `��`�� `��h��h�� !�!"�!#�!$�$%�$&�$'�'(�')�'*��+�+,�,-�-.�-/�-0�01�02�03�34�35�36�67�68�69�9:�9;�9<�<=�<>�<?��@�@A�AB��B��</structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:45:56Z</structure-indexed-at> </compound>

122703 <common-name>Allyltris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)stannane</common-name> <description>Allyltris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)stannane belongs to the organotin compounds, a subclass of organo-post-transition metal compounds within the organic compounds. With an average molecular weight of 1,201 g/mol, Allyltris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)stannane is a heavy molecule. It is characterized by the chemical formula C27H17F39Sn. The compound is found in or released from 13 recorded sources across several sectors. In electrical and electronic equipment, it is associated with cell phones, capacitors, wires and cables, batteries, and printed circuit boards, among one other source. Within the textiles, leather and furnishings sector, it is found in carpets, rugs, and synthetic textiles. It is also present in food packaging within the food, food processing and cookware sector, and in medical devices within the healthcare, pharmaceuticals and veterinary products sector. Additionally, the compound is used as lubricants in both the energy, oil and gas sector and the industrial manufacturing and chemical processing sector, as well as in one other sector. Recorded routes of exposure for this substance include inhalation, oral ingestion, and touch.</description> <cas>192212-66-1</cas> <pubchem-id>10510526</pubchem-id> <chemical-formula>C27H17F39Sn</chemical-formula> <weight>1201.1</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">2026-04-06T06:01:16Z</created-at> <updated-at type="dateTime">2026-08-17T20:46:59Z</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>FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)CC[Sn](CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)(CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)CC=C</moldb-smiles> <moldb-formula>C27H17F39Sn</moldb-formula> <moldb-inchi>InChI=1S/3C8H4F13.C3H5.Sn/c3*1-2-3(9,10)4(11,12)5(13,14)6(15,16)7(17,18)8(19,20)21;1-3-2;/h3*1-2H2;3H,1-2H2;</moldb-inchi> <moldb-inchikey>RMDIHFFKXXTNGQ-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">1201.081</moldb-average-mass> <moldb-mono-mass type="decimal">1201.972951</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp nil="true"/> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id>8685927</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>CHEM118596</chemdb-id> <dsstox-id>DTXSID40440946</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00110212</susdat-id> <iupac>(Prop-2-en-1-yl)tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)stannane</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>Organometallic compounds</superklass> <klass>Organo-post-transition metal compounds</klass> <subklass>Organotin compounds</subklass> <paper-count type="integer">0</paper-count> <sync-id>CED0108997</sync-id> <structure-inchikey>RMDIHFFKXXTNGQ-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>100000800000002000000000000000000000000000000000000000000000000000000000000000000000000000000002000000000000000020000000000000000000000000000000000000008000000200000000000000000000000000000000000000000800000200000008000008000000080000000000000000000800000000000000000000000000000200080000080000000000010080000000080000000000000200000002000000000000040000000000000000000000002000000000000000000000040000000000000000000000000000000000000000000000000000000000000000000000800004000000000000000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle>ï¾Þ��C��B��€� � �� `��`��2 ��`��`�� `��`�� `��h��h�� !�!"�!#�!$�$%�$&�$'�'(�')�'*��+�+,�,-�-.�-/�-0�01�02�03�34�35�36�67�68�69�9:�9;�9<�<=�<>�<?��@�@A�AB��B��</structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:45:56Z</structure-indexed-at> </compound>