Category
Atenolol
CAS Number
29277-73-4
Molecular Formula
C₁₄H₂₀N₂O₂
Molecular Weight
248.3 g/mol
Synonym

[4-[(2RS)-2-Hydroxy-3-[(propan-2-yl)amino]propoxy]phenyl]acetonitrile ; 2-[4-[(2RS)-2-hydroxy-3-[(1-methylethyl)amino]propoxy]phenyl]acetonitrile;Atenolol Impurity H; [p-[2-hydroxy-3-(isopropylamino)propoxy]phenyl]acetonitrile;

Keywords
High-Quality Pharmaceutical Reference Standards
Intermediates
Impurities
Pharmaceutical Standards
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.

Atenolol EP Impurity H (Molecular Formula: C₁₄H₂₀N₂O₂) is a pharmaceutical impurity reference material intended for chromatographic impurity analysis, related compound determination, assay support, degradation profiling, analytical procedure verification, and quality assessment of atenolol formulations. Manasa Life Sciences is an India-based manufacturer and supplier of pharmaceutical impurity standards, certified reference materials, API impurities, and analytical compounds, providing custom impurity synthesis, structural identification, purity assessment, forced degradation evaluation, and analytical characterization using HPLC, LC-MS/MS, NMR, FTIR, GC, qNMR, and TGA. Our products and services are supported by appropriate quality documentation, including COA and MSDS/SDS, and are designed to assist pharmaceutical manufacturers and analytical laboratories with ICH, EMA, European Pharmacopoeia (EP), and United States Pharmacopeia (USP) requirements for impurity assessment, quality control, and regulatory compliance.