N-Nitroso Eltrombopag Amino Impurity
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Documentation

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内容: HPLC、MASS/LC-MS、1H NMR、FT-IR、含量、構造解析レポート(SER)、および製品に応じた追加分析データ。

N-Nitroso Eltrombopag Amino Impurity

● Failure Report (NAP Test) Available

カタログ番号:VE0024456
CAS番号:N/A
分子式:C13H10N2O4
分子量:258.23 g/mol

に関する追加情報 N-Nitroso Eltrombopag Amino Impurity

親薬物

Eltrombopag

IUPAC名

2′-hydroxy-3′-(nitrosoamino)-[1, 1′-biphenyl]-3-carboxylic acid

薬局方同義語

N/A

Other Synonyms

N/A

SMILES

O=C(O)C1=CC(C2=CC=CC(NN=O)=C2O)=CC=C1

InChI

InChI=1S/C13H10N2O4/c16-12-10(5-2-6-11(12)14-15-19)8-3-1-4-9(7-8)13(17)18/h1-7, 16H, (H, 14, 19)(H, 17, 18)

説明

N-Nitroso Eltrombopag Amino Impurity is an N-nitroso derivative of the secondary amine present in Eltrombopag, 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 Eltrombopag 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-Eltrombopag Amino-Impurity: Synthesis Attempts and Failure Report (NAP Test)

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