Olaparib Impurity 41
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100 % Datengenauigkeit
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0 % Toleranz bei der Produktqualität

Lagerstandorte

  • New Jersey, USA
  • Czech Republic, EU
  • Mumbai, India

* Vorbehaltlich Verfügbarkeit

Dokumentation

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Enthält: HPLC, MASS/LC-MS, 1H-NMR, FT-IR, Gehalt, Structure Elucidation Report (SER) sowie zusätzliche analytische Daten je nach Produkt.

17858-15-0Olaparib Impurity 41

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Katalog-Nr.::VE0027726
CAS-Nr.::17858-15-0
Summenformel::C12H15O5P
Molare Masse::270.22 g/mol

Zusätzliche Informationen zu CAS 17858-15-0

Parent drug

Olaparib

IUPAC-Name

Diethyl (3-oxo-1,3-dihydroisobenzofuran-1-yl)phosphonate

Pharmacopeial Synonyms

N/A

Synonyme

N/A

SMILES

O=C1OC(P(OCC)(OCC)=O)C2=C1C=CC=C2

InChI

InChI=1S/C12H15O5P/c1-3-15-18(14,16-4-2)12-10-8-6-5-7-9(10)11(13)17-12/h5-8,12H,3-4H2,1-2H3

Beschreibung

Olaparib Impurity 41 (CAS 17858-15-0) is a characterized process-related and degradation impurity detected in olaparib manufacturing and stability studies. It exhibits distinct chromatographic behavior with a reproducible retention profile, and its mass spectral and NMR signatures enable unambiguous identification and structural assignment. Control of this impurity is critical for impurity profiling, qualification and regulatory compliance; typical analytical approaches include validated HPLC/UPLC methods with MS detection and orthogonal confirmation by 1H and 13C NMR. Stability assessment, limit setting and impurity fate evaluation are integral to ensuring batch consistency and meeting ICH guidelines for specified and reporting thresholds.

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