باب
Acebutolol
رقم CAS
22568-64-5
الصيغة الجزيئية
C₁₆H₂₄N₂O₄
وزن جزيئي
308.4 g/mol
مرادف

Acebutolol EP Impurity B; Acetamide, N-[3-acetyl-4-[2-hydroxy-3-[(1-methylethyl)amino]propoxy]phenyl]; Acetamide,N-[3-acetyl-4-[2-hydroxy-3-[(1-methylethyl)amino]propoxy]phenyl]; N-[3-Acetyl-4-[2-hydroxy-3-[(1-methylethyl)amino]propoxy]phenyl]acetamide; N-{3-Acetyl-4-[2-hydroxy-3-(isopropylamino)propoxy]phenyl}acetamide; Acebutolol Related Compound B (USP);Diacetolol;

الكلمات الرئيسية
High-Quality Pharmaceutical Reference Standards
Intermediates
Pharmaceutical Standards
Fine Chemicals
Amines
Aromatics
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 trusted manufacturer and supplier of high-purity Acebutolol EP Impurity B (Diacetolol), CAS No. 22568-64-5, with molecular formula C₁₆H₂₄N₂O₄ and molecular weight 308.37 g/mol. Also known as N-[3-acetyl-4-[(2RS)-2-hydroxy-3-[(1-methylethyl)amino]propoxy]phenyl]acetamide and N-{3-Acetyl-4-[2-hydroxy-3-(isopropylamino)propoxy]phenyl}acetamide, this Acebutolol impurity reference standard is suitable for pharmaceutical impurity profiling, related-substance analysis, analytical method development, method validation, stability studies, and routine quality-control testing. Each batch is characterized using advanced analytical techniques, including HPLC, LC-MS, NMR, and IR spectroscopy, to support identity and purity assessment. Manufactured under controlled quality systems and supported by applicable GMP and GDP practices, Manasa Life Sciences provides the material with comprehensive documentation, including a Certificate of Analysis (CoA) and Safety Data Sheet (SDS/MSDS), to support pharmaceutical laboratories and regulatory quality requirements aligned with applicable USP, EP, ICH, USFDA, and EMA expectations.