97503 <common-name>1-Hexadecyl 2,3,4-tris(1,2,2,6,6-pentamethyl-4-piperidyl) butane-1,2,3,4-tetracarboxylate</common-name> <description>1-Hexadecyl 2,3,4-tris(1,2,2,6,6-pentamethyl-4-piperidyl) butane-1,2,3,4-tetracarboxylate belongs to the tetracarboxylic acids and derivatives, a subclass of carboxylic acids and derivatives within the organic compounds. It has the chemical formula C54H99N3O8. With an average molecular weight of 918.40 g/mol, 1-Hexadecyl 2,3,4-tris(1,2,2,6,6-pentamethyl-4-piperidyl) butane-1,2,3,4-tetracarboxylate is a heavy molecule.</description> <cas nil="true"/> <pubchem-id>6365992</pubchem-id> <chemical-formula>C54H99N3O8</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">2026-04-05T05:19:35Z</created-at> <updated-at type="dateTime">2026-04-05T05:19:35Z</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>CCCCCCCCCCCCCCCCOC(=O)CC(C1CC(C)(C)N(C)C(C)(C)C1)(C(O)=O)C(C(C1CC(C)(C)N(C)C(C)(C)C1)C(O)=O)(C1CC(C)(C)N(C)C(C)(C)C1)C(O)=O</moldb-smiles> <moldb-formula>C54H99N3O8</moldb-formula> <moldb-inchi>InChI=1/C54H99N3O8/c1-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31-62-45(58)32-43(47(60)64-41-36-51(6,7)56(15)52(8,9)37-41)44(48(61)65-42-38-53(10,11)57(16)54(12,13)39-42)33-46(59)63-40-34-49(2,3)55(14)50(4,5)35-40/h40-44H,17-39H2,1-16H3</moldb-inchi> <moldb-inchikey>HRYUATHWNRMWNL-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">918.399</moldb-average-mass> <moldb-mono-mass type="decimal">917.7432171</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>CHEM093396</chemdb-id> <dsstox-id>DTXSID201004986</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00059839</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>Tetracarboxylic acids and derivatives</subklass> <paper-count type="integer">0</paper-count> <sync-id>CED0177034</sync-id> <structure-inchikey>HLNSNSZMBQAMOQ-UHFFFAOYSA-N</structure-inchikey> 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