Category
Atomoxetine
CAS Number
2727370-25-2
Molecular Formula
C₁₇H₂₀FNO
Molecular Weight
273.35 g/mol
Synonym

 (S)-3-(3-Fluoro-2-methylphenoxy)-N-methyl-3-phenylpropan-1-amine; (3S)-3-(3-Fluoro-2-methylphenoxy)-N-methyl-3-phenylpropan-1-amine;

Keywords
Impurities
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 F (CAS No. 2727370-25-2), molecular formula C₁₇H₂₀FNO, molecular weight 273.35 g/mol, is a fluorinated pharmaceutical impurity and analytical reference standard identified as (3S)-3-(3-Fluoro-2-methylphenoxy)-N-methyl-3-phenylpropan-1-amine. It is suitable for pharmaceutical impurity profiling, reference standard testing, process-related impurity analysis, pharmaceutical intermediates, fine chemicals, analytical research, method development, quality assurance, and synthesis R&D. Applications include HPLC, LC-MS/MS, Mass Spectrometry, NMR, FTIR/IR, chromatographic identification, purity assessment, stability studies, and analytical method validation, supporting pharmaceutical laboratories and drug-development programs. Documentation such as COA, SDS/MSDS, specifications, and analytical data can support applications following applicable EMA, USP, EP, US FDA, and ICH quality and regulatory requirements.