Lemborexant Impurity 05 NEW

Lemborexant Impurity 05;1369763-94-9

WhatsAPP: +86 17386083646
E-mail: anna@molcoo.com

• Product Number: L072005
  English Name: Lemborexant Impurity 5
  English Alias: (1R,2S)-2-(((2,4-dimethylpyrimidin-5-yl)oxy)methyl)-2-(3-fluorophenyl)-N-(pyridin-2-yl)cyclopropanecarboxamide
  CAS Number: 1369763-94-9
  Molecular Formula: C22H21FN4O2
  Molecular Weight: 392.43
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• Product Advantages: Lemborexant Impurity 5 has extremely high purity and good chemical stability. Its precise chemical structure has strong reproducibility, which can provide a reliable standard reference for pharmaceutical impurity research. As a reference substance, it remains stable under different experimental conditions, ensuring the accuracy and consistency of test results and facilitating pharmaceutical quality control.
  Application Fields: It is mainly applied in the quality control and research and development of Lemborexant drugs. As an impurity reference standard, it is used to establish and validate the detection methods of drug impurities, ensuring the sensitivity and accuracy of detection methods. During the drug production process, it is used to monitor the impurity content, helping to optimize the production process and prevent excessive impurities. At the same time, in the study of drug stability, it can analyze the changes of impurities during storage, providing a basis for determining the shelf life of drugs.
  Background Description: Lemborexant is an important drug for the treatment of insomnia. The quality of drugs is directly related to the safety and efficacy of patients' medication. Impurities in drugs may affect drug activity and even produce toxic and side effects. Therefore, impurity research is a key part of drug research and development and quality control. As a related impurity of Lemborexant, the research on the characteristics and content of Lemborexant Impurity 5 helps to comprehensively evaluate the quality of Lemborexant drugs and ensure the safety and effectiveness of medication.
  Research Status: Currently, research on Lemborexant Impurity 5 continues to advance. In terms of detection technology, more sensitive and efficient analytical methods are constantly being explored, such as Ultra - Performance Liquid Chromatography - Mass Spectrometry (UPLC - MS) technology, to achieve accurate detection of trace impurities. In the study of impurity generation mechanisms, the causes and conditions of its formation are explored by simulating the drug synthesis and storage environment, providing theoretical support for impurity control. At the same time, the research on the interaction between this impurity and Lemborexant and its impact on drug efficacy and safety is also gradually deepening to improve the comprehensive understanding of the quality of Lemborexant drugs.

NOTE！

We can also customize related analogues and modified peptides including HPLC, MS, 1H-NMR, MS, HPLC, IR, UV, COA, MSDS.
This product is intended for laboratory use only!

WhatsAPP: +86 17386083646
E-mail: anna@molcoo.com

NEW IN STOCK!

The Molcoo Laboratory added drug impurity reference standards, including Baricitinib, Piperazine, Benzylpenicillin, Tranilast and multiple N-Nitroso drug impurities! Now available for immediate delivery!