N-Nitroso Paroxetine Impurity
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Includes: HPLC, MASS/LC-MS, 1H NMR, FT-IR, Potency, Structure Elucidation Report (SER), and additional analytical data depending on the product.

2361294-43-9N-Nitroso Paroxetine Impurity

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Catalogue No.:VE0010300
CAS No.:2361294-43-9
Mol. Formula:C19H19FN2O4
Mol. Weight:358.37 g/mol

Additional information on CAS 2361294-43-9

Parent drug

Paroxetine

IUPAC Name

(3S, 4R)-3-((Benzo[d][1, 3]dioxol-5-yloxy)methyl)-4-(4-fluorophenyl)-1-nitrosopiperidine

Pharmacopoeial Synonyms

N/A

Other Synonyms

N/A

Smiles

O=NN1C[C@@H](COC2=CC=C(OCO3)C3=C2)[C@H](C4=CC=C(F)C=C4)CC1

InChI

InChI=1S/C19H19FN2O4/c20-15-3-1-13(2-4-15)17-7-8-22(21-23)10-14(17)11-24-16-5-6-18-19(9-16)26-12-25-18/h1-6,9,14,17H,7-8,10-12H2/t14-,17-/m0/s1

Description

N-Nitroso Paroxetine Impurity is an N-nitroso derivative of the secondary amine present in Paroxetine, which is a highly characterized reference material that meets stringent regulatory standards set for nitrosamine compounds, including those set by USP, EMA, JP, and BP. This nitroso standard is essential for a variety of applications, such as analytical method development, method validation (AMV), and Quality Control (QC), particularly in the context of Paroxetine production. It is suitable for use in both Abbreviated New Drug Applications (ANDA) and New Drug Applications (NDA). This nitrosamine standard helps establish detection limits, quantify impurity levels, and ensure trace nitroso impurities in pharmaceutical products remain within FDA and EMA safety limits.

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