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Postion:Product Catalog >Cenobamate Impurity
Cenobamate Impurity
  • Cenobamate Impurity
  • Cenobamate Impurity
  • Cenobamate Impurity
  • Cenobamate Impurity
  • Cenobamate Impurity

Cenobamate Impurity NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-07-31

Product Details

Product Name: Cenobamate Impurity Min. Order: 10mg
Purity: 99%+ HPLC Supply Ability: 1000
Release date: 2025/07/31

Cenobamate Impurity 

Article illustration

WhatsAPP: +86 17320513646
E-mail: anna@molcoo.com

    • Product Information

      • Product Number: C099009

      • English Name: Cenobamate Impurity 9

      • English Alias: diisopropyl 2-(2-chlorobenzoyl)malonate

      • CAS Number: None

      • Molecular Formula: C16H19ClO5

      • Molecular Weight: 326.77

    • Advantages: As a reference standard for Cenobamate Impurity 9, it has an accurate chemical structure and high purity, with stable properties under different environmental conditions and can maintain consistent quality for a long time. Its strict quality control process can provide accurate and reliable references for the quality inspection of Cenobamate-related products, effectively ensuring the accuracy and repeatability of impurity detection results, and helping to improve the drug quality control system.

    • Applications: It is mainly used in the quality research, impurity analysis, and quality control of Cenobamate bulk drugs and formulations. It can be used to establish and validate impurity detection methods such as high-performance liquid chromatography (HPLC) and gas chromatography - mass spectrometry (GC - MS). In the research and development stage of Cenobamate, it helps to study the source and generation mechanism of impurities, thereby optimizing the synthesis process and reducing impurity generation. During the production process, it is used to monitor the content of this impurity in products in real-time to ensure that drugs meet quality standards. It can also be used to evaluate the changes of impurities in Cenobamate drugs during storage and transportation, providing important evidence for drug stability research.

    • Background Description: Cenobamate is a drug used for the treatment of nervous system diseases. In the process of its research, development, and production, the presence of impurities may affect the safety, effectiveness, and stability of the drug. To ensure the safety of patients' medication and improve drug quality, strict research and precise control of impurities in Cenobamate are essential. As one of the potential impurities of Cenobamate, in-depth research on Cenobamate Impurity 9 helps to improve the quality standard system of Cenobamate, meet drug regulatory requirements, and promote the drug research and development and production process.

    • Research Status: Currently, the research on Cenobamate Impurity 9 focuses on the optimization and upgrading of impurity analysis methods, improving the sensitivity and accuracy of detecting trace impurities by improving detection technology. At the same time, active exploration is being carried out on the source and change rules of this impurity during the synthesis and storage of Cenobamate, in order to optimize the process and reduce impurity content. In addition, the research on the impact of this impurity on the performance and safety of Cenobamate drugs is also gradually underway, aiming to provide a more comprehensive and scientific basis for the overall evaluation of Cenobamate 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 17320513646
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! 





Company Profile Introduction

1. Drug standards and drug impurity reference substances: provide more than 20,000 kinds of spot impurity reference substances, with sufficient supply and same-day delivery. We have a professional R&D team and comprehensive quality control testing to ensure product quality and reliability. 2. Customized synthesis of impurities and new molecules: Quickly respond to the customized needs of CDE impurities, stably supply impurities that have established quality standards, and provide customized synthesis services for new compounds in the research and development of innovative drugs. 3. Preparation and separation of unknown impurities: With a professional impurity preparation and separation technical team and SFC preparation and separation instruments, we can solve the problems of impurity preparation in complex projects. 4. Process development of new drug intermediates: provide the supply of new drugs and new molecular impurities, process optimization services, as well as the screening and impurity analysis of commercialization routes. 5. Peptide synthesis: Provide customized peptide synthesis services, and cover all kinds of degradation impurities and process impurities generated in the research and development of peptide drugs. At the same time, it provides comprehensive structural confirmation data and customized testing services.

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