Category
viloxazine
Nitrosamine Impurities
CAS Number
NA
Molecular Formula
C₂₆H₃₇N₃O₇
Molecular Weight
503.6 g/mol
Synonym

N-(3-(2-Ethoxyphenoxy)-2-hydroxypropyl)-N-(2-(2-((2-ethoxyphenoxy)methyl)morpholino)ethyl)nitrous amide

Keywords
Impurities
Pharmaceutical Standards
Amines
Fine Chemicals
Nitrosamine Standards
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.

Designed specifically for nitrosamine risk assessment, pharmaceutical impurity monitoring, API characterization, genotoxic impurity evaluation, trace-level quantification, and regulatory analytical testing, N-Nitroso Viloxazine Impurity 8 (Molecular Formula: C₂₆H₃₇N₃O₇; Molecular Weight: 503.6 g/mol) serves as an essential Viloxazine nitrosamine impurity standard. Serving customers across Asia, Europe, Africa, the GCC, and the UAE with reliable, regulatory-compliant solutions, our product empowers advanced LC-MS, HPLC, comprehensive impurity profiling, analytical method optimization, method verification, stability-indicating analysis, pharmaceutical QC, QA, and drug-development research. 

Manasa Life Sciences, an esteemed Indian manufacturer and supplier of certified pharmaceutical reference standards, impurities, API intermediates, and fine chemicals, proudly provides this high-purity compound. Fully supporting rigorous nitrosamine testing strategies and global regulatory compliance programs, every batch is delivered with an exhaustive certificate of analysis, safety data sheet, detailed specifications, and robust analytical data including NMR and IR while strictly adhering to elite GMP and GDP frameworks to align seamlessly with relevant ICH, EMA, USP, EP, and USFDA quality expectations.