N-Nitroso Darolutamide Amine Impurity
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재고 위치

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

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Documentation

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포함 사항: HPLC, MASS/LC-MS, 1H NMR, FT-IR, 함량, 구조 규명 보고서(SER), 그리고 제품에 따라 추가 분석 데이터가 제공됩니다.

N-Nitroso Darolutamide Amine Impurity

● Under Development

카탈로그 번호:VE0027832
CAS 번호:N/A
분자식:C19H20ClN7O3
분자량:429.86 g/mol

에 대한 추가 정보

모약물

Darolutamide

IUPAC명

(S)-5-acetyl-N-(1-(3-(4-(aminomethyl)-3-chlorophenyl)-1H-pyrazol-1-yl)propan-2-yl)-1-nitroso-1H-pyrazole-3-carboxamide

Pharmacopeial Synonyms

N/A

동의어

N/A

SMILES

ClC1=C(CN)C=CC(C2=NN(C=C2)C[C@H](C)NC(C3=NN(N=O)C(C(C)=O)=C3)=O)=C1

InChI

InChI=1S/C19H20ClN7O3/c1-11(22-19(29)17-8-18(12(2)28)27(24-17)25-30)10-26-6-5-16(23-26)13-3-4-14(9-21)15(20)7-13/h3-8,11H,9-10,21H2,1-2H3,(H,22,29)/t11-/m0/s1

설명

N-Nitroso Darolutamide Amine Impurity is a nitrosamine-related degradant formed by nitrosation of darolutamide's amine moiety, raising genotoxicity and regulatory concern. Chemically characterized by an N-nitroso functional group, the impurity can arise during synthesis, purification or storage when nitrosating agents, nitrites or acidic conditions are present. Analytical control relies on sensitive LC-MS/MS and GC-MS methods with sample enrichment, stable isotope dilution and validated limits of detection. Risk mitigation includes raw material screening, control of nitrite levels, pH management, scavengers and optimized workup, coupled with forced degradation studies and stability testing to support specification setting and batch release decisions.

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