Atomoxetine N-Desmethyl Impurity

SZ CAT No:	SZ-A036012
CAS No	881995-46-6
Mol.F.	C16H19NO : HCl
Mol.Wt.	241.3 : 36.5
Inv. Status	Under QC Approval
Rel. CAS No	109306-10-7 (free base)

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Chemical Name: (3RS)-3-(2-Methylphenoxy)-3-phenylpropan-1-amine hydrochloride ;

Synonym: N-Desmethyl Atomoxetine Hydrochloride

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Smiles: NCCC(OC1=CC=CC=C1C)C2=CC=CC=C2.Cl

A quality by design approach to impurity method development for atomoxetine hydrochloride (LY139603)
Peter F. Gavin ∗, Bernard A. Olsen
Journal of Pharmaceutical and Biomedical Analysis 46 (2008) 431–441

Determination of the enantiomer and positional isomer impurities in atomoxetine hydrochloride with liquid chromatography using polysaccharide chiral stationary phases
Jane A. Sellers, Bernard A. Olsen ∗, Paul K. Owens, Peter F. Gavin
Journal of Pharmaceutical and Biomedical Analysis 41 (2006) 1088–1094

Development and validation of RP-HPLC method for the determination of Atomoxetine Hydrochloride in Pharmaceutical Dosage Forms
Gurmeet Chhabra*, Chandraprakash Jain, Saurabh K Banerjee
Int. J. Drug Dev. & Res., Oct-Dec 2011, 3 (4): 275-279

Atomoxetine N-Desmethyl Impurity is chemically (3RS)-3-(2-Methylphenoxy)-3-phenylpropan-1-amine hydrochloride ;. It is also known as N-Desmethyl Atomoxetine Hydrochloride. Atomoxetine N-Desmethyl Impurity is supplied with detailed characterization data compliant with regulatory guideline. Atomoxetine N-Desmethyl Impurity can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Atomoxetine .

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.

Atomoxetine N-Desmethyl Impurity

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