Category
Atomoxetine
CAS Number
56161-70-7
Alternate CAS Number
873310-33-9(HCL)
Molecular Formula
C₁₆H₁₉NO
Molecular Weight
241.33 g/mol
Synonym

N-Methyl-γ-phenoxybenzenepropanamine;N-Methyl-3-phenoxy-3-phenylpropan-1-amine;

Keywords
Impurities
Pharmaceutical Standards
Intermediates
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.

Atomoxetine EP Impurity A is a pharmaceutical impurity standard and analytical reference material, available as CAS No. 56161-70-7 (Free Base) and 873310-33-9 (HCl), with molecular formula C₁₆H₁₉NO and molecular weight 241.33 g/mol. Also known as N-Methyl-γ-phenoxybenzenepropanamine / N-Methyl-3-phenoxy-3-phenylpropan-1-amine, it is used for Atomoxetine impurity profiling, HPLC impurity analysis, LC-MS characterization, analytical method development, pharmaceutical quality control, research, and pharmaceutical standards/intermediates. Manasa Life Sciences, India, a trusted manufacturer and supplier, provides reliable API impurity standards, reference compounds, and pharmaceutical intermediates, with COA and SDS/MSDS documentation as applicable, supporting analytical and regulatory requirements in accordance with relevant ICH, EMA, USP, and EP (European Pharmacopoeia) guidelines.