Category
viloxazine
Nitrosamine Impurities
CAS Number
NA
Molecular Formula
C₁₃H₂₀N₂O₈S
Molecular Weight
364.37 g/mol
Synonym

2-((3-(2-ethoxyphenoxy)-2-hydroxypropyl)(nitroso)amino)ethyl hydrogen sulfate

Keywords
Pharmaceutical Standards
Nitrosamine Standards
Metabolites.
Fine Chemicals
Intermediates
N-Nitrosamines Impurities manufacturers 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.

For critical pharmaceutical testing applications, N-Nitroso Viloxazine Impurity 9 (Weight: 364.37 g/mol; Formula: C₁₃H₂₀N₂O₈S) stands as a high-purity reference standard designed for advanced nitrosamine risk assessment, genotoxic impurity evaluation, API characterization, and trace-level quantification. Delivering dependable and regulatory-compliant solutions to clients across the GCC, Europe, Asia, Africa, and the UAE, Manasa Life Sciences operates as an Indian manufacturer and supplier specializing in certified reference standards, fine chemicals, intermediates, and impurities.

Strict adherence to elite GDP and GMP frameworks ensures that our offerings seamlessly align with the stringent quality expectations of USFDA, EP, USP, EMA, and ICH guidelines, supporting comprehensive global nitrosamine testing strategies. Empowering stability-indicating analysis, LC-MS, HPLC, method optimization, impurity profiling, QA, QC, and drug-development R&D, every single batch comes fully equipped with precise technical specifications, reliable spectral data (IR, NMR), an exhaustive COA, and a transparent SDS/MSDS.