Category
Atomoxetine
CAS Number
2706536-33-4
Molecular Formula
C₁₀H₁₅NO
Molecular Weight
165.23 g/mol
Synonym

 3-(methylamino)-1-phenylpropan-1-ol;Fluoxetine Hydrochloride - Impurity A(EP); (±)-N-Methyl-3-hydroxy-3-phenylpropylamine; 3-(Methylamino)-1-phenyl-1-propanol; α[(2-Methylamino)ethyl] benzyl alcohol; Aminomethyl-1-phenylpropanol; -Methylamino-1-phenylpropan-1-ol; α-[2-(methylamino)ethyl]benzenemethanol; Atomoxetine Related Compound A (USP);

Keywords
Fine Chemicals
Pharmaceutical Standards
Metabolites.
Impurities
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 H (CAS 42142-52-9; C₁₀H₁₅NO; 165.23 g/mol) is a key Atomoxetine-related compound and pharmaceutical analytical standard, chemically known as 3-(Methylamino)-1-phenylpropan-1-ol and recognized as Atomoxetine Related Compound A (USP). Manasa Life Sciences, a leading India-based manufacturer and supplier of pharmaceutical reference materials, provides this impurity for API characterization, impurity identification, forced degradation studies, extractables and leachables research, chromatographic method optimization, pharmaceutical process monitoring, drug-development analytics, and quality assessment. It is applicable to HPLC/UPLC, LC-MS, GC-MS, NMR, FTIR, assay and purity determination, peak identification, stability-indicating methods, and analytical validation, with COA, SDS/MSDS, specifications, and supporting analytical data available for research and quality-control applications under relevant ICH, EMA, USP, EP, and US FDA expectations.