Category
Benzydamine
CAS Number
1797879-37-8
Alternate CAS Number
2196183-71-6 (HCl Salt)
Molecular Formula
C₂₆H₂₉N₃O
Molecular Weight
399.53 g/mol
Synonym

3-(1,5-Dibenzyl-1H-indazol-3-yl)oxypropyldimethylamine ; 5-Benzyl Benzydamine; 3-((1,5-Dibenzyl-1H-indazol-3-yl)oxy)-N,N-dimethylpropan-1-amine;

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.

Manasa Life Sciences supplies Benzydamine EP Impurity B (CAS No. 1797879-37-8) and Benzydamine EP Impurity B Hydrochloride Salt (CAS No. 2196183-71-6) as pharmaceutical impurity reference standards for analytical research, method development, impurity profiling, related-substance analysis, and API quality-control applications. Benzydamine EP Impurity B is the free-base form, with a molecular formula of C₂₆H₂₉N₃O and a molecular weight of 399.53 g/mol. The material supports pharmaceutical impurity identification, HPLC method validation, LC-MS analysis, ¹H NMR and ¹³C NMR characterization, FTIR spectroscopy, and stability-indicating analytical studies.

As a trusted supplier of pharmaceutical impurity standards and API reference materials, Manasa Life Sciences serves pharmaceutical manufacturers, quality-control laboratories, contract research organizations (CROs), and analytical research institutions across India, the UAE, GCC countries, Asia, Europe, and Africa. Product-specific documentation, including Certificate of Analysis (COA), SDS/MSDS, HPLC chromatograms, spectral characterization reports, and batch traceability records, may be provided subject to availability. These reference standards are intended to support testing activities aligned with applicable ICH, USP, EP, EMA, and WHO regulatory guidelines.