Amisulpride EP Impurity A

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 an India-based manufacturer and supplier of high-quality pharmaceutical reference standards and analytical impurities, offering reliable solutions for pharmaceutical and research applications. Amisulpride EP Impurity A (CAS No. 26116-12-1; Molecular Formula: C₇H₁₆N₂; Molecular Weight: 128.2 g/mol) is a pharmaceutical impurity reference standard used for impurity profiling, analytical testing, quality control, method development, method validation, and R&D applications. Manasa Life Sciences provides comprehensive analytical testing services supported by expert scientists and stringent quality-control practices. Complete analytical documentation can include HPLC, Mass, FTIR, NMR, GC, Potency, and COA, along with relevant technical and quality documentation. Our products and analytical solutions are aligned with applicable ICH, EMA, EP, and USP guidelines, providing reliable and regulatory-compliant support for pharmaceutical, industrial, and research applications across India, Asia, Europe, Africa, the GCC, and the UAE.