Category
Acalabrutinib
CAS Number
1420477-60-6
Alternate CAS Number
2242394-65-4(Maleate Salt);2641500-53-8(Maleate Monohydrate salt)
Molecular Formula
C₂₆H₂₃N₇O₂
Molecular Weight
465.52 g/mol
Synonym

4-[8-Amino-3-[(2S)-1-(1-oxo-2-butyn-1-yl)-2-pyrrolidinyl]imidazo[1,5-a]pyrazin-1-yl]-N-2-pyridinylbenzamide; (S)-4-(8-Amino-3-(1-(but-2-ynoyl)pyrrolidin-2-yl)imidazo[1,5-a]pyrazin-1-yl)-N-(pyridin-2-yl)benzamide; (S)-4-[8-Amino-3-[1-(but-2-ynoyl)pyrrolidin-2-yl]imidazo[1,5-a]pyrazin-1-yl]-N-(pyridin-2-yl)benzamide; Calquence;

Keywords
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 Standard (CAS No. 1420477-60-6), with a molecular formula of C₂₆H₂₃N₇O₂ and molecular weight 465.52 g/mol, is an important reference standard used in pharmaceutical analysis and drug development. It plays a crucial role in ensuring the quality, safety, and efficacy of acalabrutinib-based formulations.

This standard is widely utilized for impurity profiling, analytical method development, and validation processes. It supports accurate and reliable quantification when used with advanced analytical techniques such as HPLC, LC-MS/MS, and NMR.

Based in Hyderabad, India, Manasa Life Sciences manufactures and supplies high-purity Acalabrutinib Standard to pharmaceutical markets across Asia, Europe, Africa, the GCC, and the UAE. The company ensures full traceability and compliance with Good Documentation Practices (GDP), delivering certified reference standards of consistent quality. Its expert scientific team provides services in impurity profiling, method validation, and risk assessment, helping pharmaceutical manufacturers meet USP, EP, ICH, and FDA regulatory requirements while maintaining high standards of product quality.