Lemborexant Impurity 09;1369768-30-8
WhatsAPP: +86 17386083646
E-mail: anna@molcoo.com
Product Number: L072009
English Name: Lemborexant Impurity 9
English Alias: ((1S,2R)-1-(3-fluorophenyl)cyclopropane-1,2-diyl)bis(methylene) diacetate
CAS Number: 1369768-30-8
Molecular Formula: C15H17FO4
Molecular Weight: 280.29
Product Advantages: Lemborexant Impurity 9 has high purity, good chemical stability and uniformity. It can maintain stable properties in various experimental environments. As a reference substance, it can provide a reliable benchmark for pharmaceutical impurity analysis, enabling accurate and highly reproducible detection, and ensuring the accuracy and effectiveness of data in pharmaceutical quality research.
Application Fields: It is mainly applied in the research, development and quality control of Lemborexant drugs. As an impurity reference standard, it is used to establish and optimize the detection methods of Lemborexant impurities, and verify the accuracy and sensitivity of analytical methods. During the drug production process, it can monitor the impurity content and assist in optimizing the production process to ensure that the impurity level of drugs meets the standards. When investigating drug stability, it helps to analyze the changes of impurities during storage, providing important basis for determining the shelf life and storage conditions of drugs.
Background Description: Lemborexant is used to treat insomnia, and its drug quality is related to the safety and treatment effect of patients' medication. Impurities in drugs may interfere with drug activity, affect drug stability and even bring potential risks. Impurity research is a key part of drug research and development, production and quality control. As a related impurity of Lemborexant, in - depth research on Lemborexant Impurity 9 helps to comprehensively control the quality of Lemborexant drugs and ensure the safety of clinical medication.
Research Status: Currently, research on Lemborexant Impurity 9 is continuously deepening. In terms of detection technology, more advanced analytical methods, such as high - resolution mass spectrometry technology, are constantly being explored to achieve accurate qualitative and quantitative analysis of trace impurities. In the study of impurity generation mechanisms, the causes and influencing factors of its formation are analyzed by simulating drug synthesis routes and storage environments, providing theoretical support for source control of impurities. At the same time, research on the impact of this impurity on the safety and effectiveness of Lemborexant drugs has also been gradually carried out, aiming to more comprehensively evaluate drug quality.
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
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