Category
Atomoxetine
CAS Number
1643684-02-9
Alternate CAS Number
1643684-05-2(HCl Salt)
Molecular Formula
C₁₇H₂₁NO
Molecular Weight
255.36 g/mol
Synonym

 (3R)-N-methyl-3-(3-methylphenoxy)-3-phenylpropan-1-amine;(R)-N-Methyl-3-phenyl-3-(m-tolyloxy)propan-1-amine; m-Methyl Atomoxetine;

Keywords
Intermediates
Pharmaceutical Standards
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.

Atomoxetine EP Impurity D (CAS No. 1643684-02-9; HCl Salt CAS No. 1643684-05-2) is a high-quality pharmaceutical impurity reference standard with molecular formula C₁₇H₂₁NO and molecular weight 255.36 g/mol, chemically identified as (3R)-N-methyl-3-(3-methylphenoxy)-3-phenylpropan-1-amine, also known as (R)-N-Methyl-3-phenyl-3-(m-tolyloxy)propan-1-amine and m-Methyl Atomoxetine. This specialty compound is suitable for pharmaceutical impurity profiling, analytical reference standards, pharmaceutical intermediates, fine chemicals, method development, process development, quality control, stability studies, and synthesis R&D. It supports HPLC, LC-MS/MS, Mass Spectrometry, NMR, FTIR/IR, chromatographic purity, identification, assay, and analytical method validation applications in pharmaceutical research and development. Manasa life Sciences As a reliable  Manufacturer and supplier in india with a focus on quality, traceability, regulatory compliance, and research-grade consistency, Atomoxetine EP Impurity D can be supported with COA, HPLC chromatogram, MSDS/SDS, specification sheet, analytical data, and appropriate laboratory documentation for pharmaceutical development, impurity testing, formulation research, and quality assurance applications.