97828 <common-name>2,4-Dinonylphenyl bis(4-nonylphenyl) phosphite</common-name> <description>2,4-Dinonylphenyl bis(4-nonylphenyl) phosphite belongs to the phenoxy compounds, a subclass of benzene and substituted derivatives within the organic compounds. It is classified as a benzenoid with the chemical formula C54H87O3P. With an average molecular weight of 815.26 g/mol, 2,4-Dinonylphenyl bis(4-nonylphenyl) phosphite is a heavy molecule.</description> <cas>85030-49-5</cas> <pubchem-id>5743893</pubchem-id> <chemical-formula>C54H87O3P</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">2026-04-05T05:31:17Z</created-at> <updated-at type="dateTime">2026-04-05T05:31:17Z</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>CCCCCCCCCC1=CC=C(OP(OC2=CC=C(CCCCCCCCC)C=C2)OC2=C(CCCCCCCCC)C=C(CCCCCCCCC)C=C2)C=C1</moldb-smiles> <moldb-formula>C54H87O3P</moldb-formula> <moldb-inchi>InChI=1/C54H87O3P/c1-5-9-13-17-21-25-29-33-48-37-42-52(43-38-48)55-58(56-53-44-39-49(40-45-53)34-30-26-22-18-14-10-6-2)57-54-46-41-50(35-31-27-23-19-15-11-7-3)47-51(54)36-32-28-24-20-16-12-8-4/h37-47H,5-36H2,1-4H3</moldb-inchi> <moldb-inchikey>LDLQMIVOOISNKJ-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">815.261</moldb-average-mass> <moldb-mono-mass type="decimal">814.6392833</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>CHEM093721</chemdb-id> <dsstox-id>DTXSID70234097</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00060254</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>Benzenoids</superklass> <klass>Benzene and substituted derivatives</klass> <subklass>Phenoxy compounds</subklass> <paper-count type="integer">0</paper-count> <sync-id>CED0088484</sync-id> <structure-inchikey>LDLQMIVOOISNKJ-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>4000000000408000000800200800000000000000000000000000000000000000000000002000200200000000000000000000000000000000000000000000000000000000000020000010000004000000000000000000100000200000000000000000020000000000000000800100000000000000000000000002000000000000000040040000000000000000000010000000000800000000000001000080000000000000000000004000000080000000000000008000000000002000000010000000000000000000000000000000000000000000000000000000220000000000000000000000000000040000000010080000000000020000000000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle type="binary" encoding="base64">776t3gAAAAAQAAAAAwAAAAAAAAA6AAAAPAAAAIABBgBgAAAAAQMGAGAAAAAC AgYAYAAAAAICBgBgAAAAAgIGAGAAAAACAgYAYAAAAAICBgBgAAAAAgIGAGAA AAACAgYAYAAAAAICBkAoAAAAAwQGQGgAAAADAwEGQGgAAAADAwEGQCgAAAAD BAgAKAAAAAMCDwAgAAAAAwgAKAAAAAMCBkAoAAAAAwQGQGgAAAADAwEGQGgA AAADAwEGQCgAAAADBAYAYAAAAAICBgBgAAAAAgIGAGAAAAACAgYAYAAAAAIC BgBgAAAAAgIGAGAAAAACAgYAYAAAAAICBgBgAAAAAgIGAGAAAAABAwZAaAAA AAMDAQZAaAAAAAMDAQgAKAAAAAMCBkAoAAAAAwQGQCgAAAADBAYAYAAAAAIC BgBgAAAAAgIGAGAAAAACAgYAYAAAAAICBgBgAAAAAgIGAGAAAAACAgYAYAAA AAICBgBgAAAAAgIGAGAAAAABAwZAaAAAAAMDAQZAKAAAAAMEBgBgAAAAAgIG AGAAAAACAgYAYAAAAAICBgBgAAAAAgIGAGAAAAACAgYAYAAAAAICBgBgAAAA AgIGAGAAAAACAgYAYAAAAAEDBkBoAAAAAwMBBkBoAAAAAwMBBkBoAAAAAwMB BkBoAAAAAwMBCwABAAECAAIDAAMEAAQFAAUGAAYHAAcIAAgJAAkKaAwKC2gM CwxoDAwNIA0OAA4PAA8QIBARaAwREmgMEhNoDBMUABQVABUWABYXABcYABgZ ABkaABobABscABMdaAwdHmgMDh8AHyAgICFoDCEiACIjACMkACQlACUmACYn ACcoACgpACkqACEraAwrLGgMLC0ALS4ALi8ALzAAMDEAMTIAMjMAMzQANDUA LDZoDDY3aAwMOGgMODloDDkJaAweEGgMNyBoDEIDAAAABgk5OAwLCgYREhMd HhAGISssNjcgFwQAAAAAAAAAFg== </structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:37:46Z</structure-indexed-at> </compound>