Category
Atomoxetine
CAS Number
STD - 83015-26-3 ; IMP - A - 56161-70-7
Molecular Formula
STD - C₁₇H₂₁NO ; IMP - A - C₁₆H₁₉NO;
Molecular Weight
STD - 255.35 g/mol ; IMP - A - 241.33 g/mol;
Synonym

Atomoxetine STD - Atomexine; (R)-N-Methyl-γ-(2-methyl­phenoxy)benzenepropanamine; (R)-N-methyl-3-phenyl-3-(o-tolyloxy)propan-1-amine; Atomoxetine (USP);                                                                                                                Atomoxetine EP Impurity A - 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
Pharmaceutical Standards
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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 Standard & Atomoxetine EP Impurity A — Atomoxetine STD (CAS No. 83015-26-3, molecular formula C₁₇H₂₁NO, molecular weight 255.35 g/mol) and Atomoxetine EP Impurity A (CAS No. 56161-70-7, molecular formula C₁₆H₁₉NO) are pharmaceutical reference materials used for API identification, impurity characterization, chromatographic profiling, assay and purity testing, analytical method development, and quality control. Atomoxetine is also known as Atomexine, (R)-N-Methyl-γ-(2-methylphenoxy)benzenepropanamine, (R)-N-methyl-3-phenyl-3-(o-tolyloxy)propan-1-amine, and Atomoxetine (USP), while Impurity A is identified as N-Methyl-γ-phenoxybenzenepropanamine and N-Methyl-3-phenoxy-3-phenylpropan-1-amine. Manasa Life Sciences, a leading manufacturer and supplier in India, provides pharmaceutical standards, impurity reference materials, intermediates, and fine chemicals for HPLC, UHPLC, LC-MS, NMR, FTIR, method validation, stability assessment, process development, and pharmaceutical R&D, with COA, SDS/MSDS, specifications, and analytical documentation available for laboratory and quality-assurance applications.