Atenolol EP Impurity E

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.

Atenolol EP Impurity E (CAS No. 141650-31-9; Molecular Formula: C₁₉H₂₂N₂O₅; Molecular Weight: 358.4 g/mol) is a high-quality pharmaceutical impurity reference standard suitable for analytical testing, impurity profiling, trace-level detection, and pharmaceutical quality control. It is applicable to HPLC and LC-MS/MS analysis, related substances testing, analytical method development and validation, stability-indicating studies, degradation product identification, and pharmaceutical research.

Manasa Life Sciences is a trusted manufacturer and supplier in India of pharmaceutical impurities, reference standards, APIs, and research compounds, offering advanced analytical characterization services including HPLC, LC-MS/MS, NMR, FTIR, GC, qNMR, and TGA, supported by COA, MSDS/SDS, GLP, and GDP documentation. Our scientific team provides specialized support for impurity characterization, structural elucidation, custom impurity synthesis, process impurity evaluation, forced degradation studies, stability testing, analytical method optimization, and validation, supporting pharmaceutical R&D, quality control, regulatory testing, and drug development programs.

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