92477 <common-name>Tetrakis(acetoxydibutylstannyloxy)silane</common-name> <description>Tetrakis(acetoxydibutylstannyloxy)silane belongs to the carboxylic acid derivatives, a subclass of carboxylic acids and derivatives within the organic compounds. It has the chemical formula C40H84O12SiSn4. With an average molecular weight of 1,260 g/mol, Tetrakis(acetoxydibutylstannyloxy)silane is a heavy molecule.</description> <cas nil="true"/> <pubchem-id nil="true"/> <chemical-formula>C40H84O12SiSn4</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">2026-04-05T01:34:17Z</created-at> <updated-at type="dateTime">2026-04-05T01:34:17Z</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>CCCC[Sn](CCCC)(OC(C)=O)O[Si](O[Sn](CCCC)(CCCC)OC(C)=O)(O[Sn](CCCC)(CCCC)OC(C)=O)O[Sn](CCCC)(CCCC)OC(C)=O</moldb-smiles> <moldb-formula>C40H84O12SiSn4</moldb-formula> <moldb-inchi>InChI=1/8C4H9.4C2H4O2.O4Si.4Sn/c8*1-3-4-2;4*1-2(3)4;1-5(2,3)4;;;;/h8*1,3-4H2,2H3;4*1H3,(H,3,4);;;;;/q;;;;;;;;;;;;-4;4*+2/p-4/rC40H84O12SiSn4/c1-13-21-29-54(30-22-14-2,45-37(9)41)49-53(50-55(31-23-15-3,32-24-16-4)46-38(10)42,51-56(33-25-17-5,34-26-18-6)47-39(11)43)52-57(35-27-19-7,36-28-20-8)48-40(12)44/h13-36H2,1-12H3</moldb-inchi> <moldb-inchikey>PPDNJQIZRKFFNJ-UHFFFAOYSA-J</moldb-inchikey> <moldb-average-mass type="decimal">1260.025</moldb-average-mass> <moldb-mono-mass type="decimal">1264.181983</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp nil="true"/> <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>CHEM088370</chemdb-id> <dsstox-id>DTXSID70210750</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00053902</susdat-id> <iupac nil="true"/> <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>Carboxylic acid derivatives</subklass> <paper-count type="integer">1461</paper-count> <sync-id>CED0007418</sync-id> <structure-inchikey>PPDNJQIZRKFFNJ-UHFFFAOYSA-J</structure-inchikey> <structure-fingerprint>800000000000000800000000000000000000000000000000000000000000000000002000000000000000000002000000000000000000000000000000020000000000400000000010000000000000020000000000100000000000000000000000020010000000000000002000000000000000000000000000000000000400010000040000000000008000000050000000000080000000000000000000000000000000008000000000000000000000000000000000000000000000000000000000000000000010000000100000000000000000000000000000000000000008000000000000000000000000000010400000080000000000000000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle>ï¾­Þ����������������9���8���€���`�������`�������`�������`�����2 ������`�������`�������`�������`�������(�������(�������`�������(������� ����� ������ ����2 ������`�������`�������`�������`�������`�������`�������`�������`�������(�������(�������`�������(������� ����2 ������`�������`�������`�������`�������`�������`�������`�������`�������(�������(�������`�������(������� ����2 ������`�������`�������`�������`�������`�������`�������`�������`�������(�������(�������`�������(������������������������������� � �� �(�� � ������������������������������������� �����(����������� � !�!"��#�#$�$%�%&��'�'( ()�(*(��+�+,�,-�-.�./�/0�,1�12�23�34�,5�56 67�68(�B��������������</structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:34:33Z</structure-indexed-at> </compound>