Category
Benzydamine
CAS Number
87453-76-7
Alternate CAS Number
2196185-65-4 (HCl Salt)
Molecular Formula
C₁₉H₂₄N₂O₂
Molecular Weight
312.4 g/mol
Synonym

3-Dimethylaminopropyl 2-benzylaminobenzoate ; 2-[(Phenylmethyl)amino]benzoic Acid 3-(Dimethylamino)propyl Ester; 3-(Dimethylamino)propyl 2-(benzylamino)benzoate; 3-Dimethylaminopropyl-2-benzylaminobenzoate;

Keywords
High-Quality Pharmaceutical Reference Standards
Intermediates
Impurities
Pharmaceutical Standards
Amines
Aromatics
Fine Chemicals
Impurities manufacturer and Suppliers in Hyderabad india
Impurities Manufacturer in 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.

Benzydamine EP Impurity A, CAS No. 87453-76-7, Molecular Formula C₁₉H₂₄N₂O₂, and Molecular Weight 312.40 g/mol, is a pharmaceutical impurity reference standard used for analytical method development, impurity profiling, related substances analysis, method validation, and quality control testing of Benzydamine pharmaceutical formulations.

Manasa Life Sciences, a trusted pharmaceutical impurity standards manufacturer and supplier in India, offers Benzydamine EP Impurity A for pharmaceutical research, API impurity characterization, and analytical testing applications. Our pharmaceutical analytical reference standards support HPLC, LC-MS, ¹H NMR, ¹³C NMR, and FTIR characterization, with product-specific documentation such as Certificate of Analysis (COA), MSDS/SDS, chromatograms, spectral data, and batch traceability, subject to availability.

As a reliable Benzydamine impurity reference standard supplier in India, Manasa Life Sciences supports pharmaceutical companies, API manufacturers, contract research organizations (CROs), and quality control laboratories with reference materials for testing activities aligned with applicable ICH, USP, EP, EMA, and WHO regulatory guidelines. We serve pharmaceutical research and analytical testing requirements across India, UAE, GCC countries, Asia, Europe, and Africa.