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

* Stock subject to availability.

Documentation

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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.

N-Nitroso Sacubitril Impurity 1

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Catalogue No.:VE0010125
CAS No.:N/A
Mol. Formula:C18H18N2O2
Mol. Weight:294.35 g/mol

Additional information on N-Nitroso Sacubitril Impurity 1

Parent drug

Sacubitril

IUPAC Name

5-({[1, 1′-biphenyl]-4-yl}methyl)-3-methyl-1-nitrosopyrrolidin-2-one

Pharmacopoeial Synonyms

N/A

Other Synonyms

N/A

Smiles

O=C1N(N=O)C(CC2=CC=C(C3=CC=CC=C3)C=C2)CC1C

InChI

InChI=1S/C18H18N2O2/c1-13-11-17(20(19-22)18(13)21)12-14-7-9-16(10-8-14)15-5-3-2-4-6-15/h2-10,13,17H,11-12H2,1H3

Description

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