باب
Acalabrutinib
رقم CAS
NA
الصيغة الجزيئية
C₅₂H₄₆N₁₄O₄
وزن جزيئي
931.03 g/mol
مرادف

4-(7-((Z)-4-((S)-2-(8-amino-1-(4-(pyridin-2-ylcarbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)pyrrolidin-1-yl)-4-oxobut-2-en-2-yl)-3-((S)-1-(but-2-ynoyl)pyrrolidin-2-yl)-8-imino-7,8-dihydroimidazo[1,5-a]pyrazin-1-yl)-N-(pyridin-2-yl)benzamide 

الكلمات الرئيسية
Intermediates
Pharmaceutical Standards
Fine Chemicals
Impurities manufacturer and Suppliers in Hyderabad india
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Purity:

Above - 95.0%

Technical Data:

We will provide complete documentation support for every Standard Material. All analytical reports such as ¹H NMR, ¹³C NMR, Mass, FT-IR, HPLC Purity/GC Purity/QNMR Purity, Water content by KF/ Loss on Drying/TGA (Thermo-gravimetric Analysis). Certificate of Analysis with potency report. Each Standard Material SER (Structure Elucidation Report) with NMR, Mass, IR spectral interpretation. This whole analytical document can be included in eCTD, ANDA, DMF submissions to regulatory agencies.

Acalabrutinib 1.69 RRT is an unidentified impurity observed during the chromatographic analysis of Acalabrutinib, monitored to ensure the drug’s quality and regulatory compliance. Studying this impurity helps in understanding degradation pathways and improving the stability and safety of the final pharmaceutical product.