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Postion:Product Catalog >Lenvatinib Impurity 80
Lenvatinib Impurity 80
  • Lenvatinib Impurity 80
  • Lenvatinib Impurity 80
  • Lenvatinib Impurity 80
  • Lenvatinib Impurity 80
  • Lenvatinib Impurity 80

Lenvatinib Impurity 80 NEW

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Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-07-02

Product Details

Product Name: Lenvatinib Impurity 80 CAS No.: 16600-22-9
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/02
Molecular formula: C12H10ClNO3

Lenvatinib Impurity 80;16600-22-9

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

  • Product Information

  • Product Number: L021080

  • English Name: Lenvatinib Impurity 80

  • English Alias: ethyl 7-chloro-4-hydroxyquinoline-3-carboxylate

  • CAS Number: 16600-22-9

  • Molecular Formula: C??H??ClNO?

  • Molecular Weight: 251.67

  • Advantages

  • As an impurity of lenvatinib, Lenvatinib Impurity 80 has a well-defined chemical structure and stable properties, and can be used as a standard reference for drug research, development, and quality control. Its presence helps to analyze the possible side reaction mechanisms during lenvatinib synthesis. Through precise impurity reference analysis, it can optimize the production process, improve product quality, and ensure that drug safety and effectiveness meet high standards.

  • Applications

  • Drug Development: In the research and development of lenvatinib and its formulations, it is used as an impurity reference standard for identification and quantitative analysis, helping to determine the impurity profile of drugs and evaluate the purity of active pharmaceutical ingredients and formulations;

  • Quality Control: As a standard substance, it is used to verify the accuracy and sensitivity of detection methods such as HPLC and LC-MS, ensuring that impurity content meets pharmacopoeia and regulatory requirements during production;

  • Stability Studies: Research on the stability of this impurity under different conditions provides data support for determining the storage conditions and shelf life of lenvatinib.

  • Background Description

  • Lenvatinib is a multi-target tyrosine kinase inhibitor widely used in the treatment of various cancers such as liver cancer and thyroid cancer. During drug synthesis and production, various impurities are inevitably generated due to factors such as reaction conditions and raw material purity. As one of these impurities, the content and properties of Lenvatinib Impurity 80 directly affect the quality of lenvatinib drugs. With the increasing requirements for drug quality and safety in the pharmaceutical industry, the research and control of this impurity have become an important part of the lenvatinib quality control system.

  • Research Status

  • Currently, research on Lenvatinib Impurity 80 mainly focuses on the development and optimization of impurity detection methods, improvement of synthesis processes, and toxicological evaluations. Researchers develop more sensitive and accurate detection technologies, such as ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS), to achieve trace detection of this impurity. At the same time, they deeply study its synthesis mechanism and optimize the production process of lenvatinib to reduce impurity generation. In addition, in vitro cell experiments and animal models are used to evaluate the potential toxicity of this impurity, providing a scientific basis for formulating reasonable impurity limit standards

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





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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