N-Nitroso Amlodipine Impurity-1
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  • New Jersey, USA
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  • Mumbai, India

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Documentation

Download MSDS

Download Sample COA

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

N-Nitroso Amlodipine Impurity-1

● Failure Report (NAP Test) Available

Catalogue No.:VE008552
CAS No.:N/A
Mol. Formula:C20H21ClN2O6
Mol. Weight:420.8 g/mol

Additional information on N-Nitroso Amlodipine Impurity-1

Parent drug

Amlodipine

IUPAC Name

5-ethyl 7-methyl 6-(2-chlorophenyl)-8-methyl-4-nitroso-3, 4, 6, 7-tetrahydro-2H-benzo[b][1, 4]oxazine-5, 7-dicarboxylate

Pharmacopeial Synonyms

N/A

Other Synonyms

N-Nitroso Amlodipine BP Impurity 1

Smiles

O=C(C1=C2C(OCCN2N=O)=C(C)C(C(OC)=O)C1C3=CC=CC=C3Cl)OCC

InChI

InChI=1S/C20H21ClN2O6/c1-4-28-20(25)16-15(12-7-5-6-8-13(12)21)14(19(24)27-3)11(2)18-17(16)23(22-26)9-10-29-18/h5-8,14-15H,4,9-10H2,1-3H3

Description

N-Nitroso Amlodipine Impurity-1 is an N-nitroso derivative of the secondary amine present in Amlodipine, 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 Amlodipine 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.

N-Nitroso-Amlodipine-Impurity-1: Synthesis Attempts and Failure Report (NAP Test)

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