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Niraparib Nitroso Impurity 3
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Stock Locations

  • New Jersey, USA
  • Czech Republic, EU
  • Mumbai, India

* Stock subject to availability.

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.

Niraparib Nitroso Impurity 3

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Catalogue No.:VE0024460
CAS No.:N/A
Mol. Formula:C20H20N4O5
Mol. Weight:396.4 g/mol

Additional information on Niraparib Nitroso Impurity 3

Parent drug

Niraparib

IUPAC Name

Methyl (S, E)-2-nitro-3-(((4-(1-nitrosopiperidin-3-yl)phenyl)imino)methyl)benzoate

Pharmacopoeial Synonyms

N/A

Other Synonyms

N/A

Smiles

O=C(OC)C1=CC=CC(/C=N/C2=CC=C([C@H]3CN(N=O)CCC3)C=C2)=C1[N+]([O-])=O

InChI

InChI=1S/C20H20N4O5/c1-29-20(25)18-6-2-4-15(19(18)24(27)28)12-21-17-9-7-14(8-10-17)16-5-3-11-23(13-16)22-26/h2, 4, 6-10, 12, 16H, 3, 5, 11, 13H2, 1H3/b21-12+/t16-/m1/s1

Description

Niraparib Nitroso Impurity 3 is an N-nitroso derivative of the secondary amine present in Niraparib | 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 Niraparib 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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