Lemborexant Impurity04;1369767-24-7
WhatsAPP: +86 17386083646
E-mail: anna@molcoo.com
Product Number: L072004
English Name: Lemborexant Impurity 4
English Alias: ((1R,2S)-2-(((2,4-dimethylpyrimidin-5-yl)oxy)methyl)-2-(3-fluorophenyl)cyclopropyl)methanol
CAS Number: 1369767-24-7
Molecular Formula: C17H19FN2O2
Molecular Weight: 302.34
Product Advantages: Lemborexant Impurity 4 has high purity and good stability. Its structure is clear and consistent, which can accurately simulate the characteristics of impurities in drugs. It provides a reliable reference substance for pharmaceutical quality research, enabling accurate detection and control of drug impurity content, and ensuring the stability and consistency of drug quality.
Application Fields: It is mainly applied in the field of pharmaceutical quality control and research. As a reference standard, it is used for impurity analysis, method validation, and quality standard establishment of Lemborexant - related drugs. In the drug research and development process, it helps researchers understand the generation and change laws of impurities during drug production and storage, thereby optimizing production processes and storage conditions to ensure the safety and effectiveness of drugs. It can also be used to evaluate the accuracy and sensitivity of drug analysis methods.
Background Description: Lemborexant is a drug used to treat insomnia. During the process of drug research and development, production, and quality control, impurity research is of great importance. The presence of impurities may affect the safety, effectiveness, and stability of drugs. As a related impurity of Lemborexant, the research on Lemborexant Impurity 4 is of great significance for comprehensively evaluating the quality of Lemborexant drugs and ensuring medication safety, which has attracted great attention from pharmaceutical companies and scientific research institutions.
Research Status: Currently, research on Lemborexant Impurity 4 mainly focuses on the development of accurate detection methods, such as the optimization and application of techniques like High - Performance Liquid Chromatography (HPLC) and Liquid Chromatography - Mass Spectrometry (LC - MS) to achieve accurate detection of impurities at lower concentrations. In terms of impurity source analysis, researchers are committed to clarifying its generation mechanism during drug synthesis reactions and storage conditions, providing a theoretical basis for controlling impurities from the source. At the same time, research on the interaction between impurities and drugs and their impact on drug efficacy and safety is also gradually deepening to improve the understanding of this impurity.
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!
China
