Category
Acebutolol
CAS Number
57898-71-2
Molecular Formula
C₂₀H₃₂N₂O₄
Molecular Weight
348.48 g/mol
Synonym

N-[3-Butanoyl-4-[(2RS)-2-hydroxy-3-[(1-methylethyl) amino] propoxy] phenyl] butanamide 

Keywords
Intermediates
High-Quality Pharmaceutical Reference Standards
Impurities
Amines
Aromatics
Fine Chemicals
Impurities Manufacturer in India
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.

Manasa Life Sciences is a specialized manufacturer and supplier of high-purity Acebutolol EP Impurity K (N-tert-Butyl Acebutolol), identified by CAS No. 74143-33-2, with the molecular formula C₂₀H₃₂N₂O₄ and a molecular weight of 348.48 g/mol. This Acebutolol-related analytical impurity, also known as 3-Deacetyl-3-Butanoyl Acebutolol, is systematically identified as N-[3-butanoyl-4-[(2RS)-2-hydroxy-3-[(1-methylethyl)amino]propoxy]phenyl]butanamide and is supplied pharmaceutical analytical applications. It is characterized using advanced analytical techniques, including HPLC, LC-MS, NMR, and IR spectroscopy, supporting impurity profiling, related-substance analysis, analytical method development, method validation, stability studies, and pharmaceutical quality-control testing. Manasa Life Sciences follows robust quality and documentation practices aligned with applicable USP, Ph. Eur. (EP), USFDA, EMA, ICH, GMP, and GDP requirements. Each batch is supplied with comprehensive documentation, including a Certificate of Analysis (CoA) and Safety Data Sheet (SDS/MSDS), supporting traceability, consistent quality, and reliable use as an analytical reference standard in pharmaceutical research, development, and quality assurance.