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Postion:Product Catalog >Lapatinib Impurity9
Lapatinib Impurity9
  • Lapatinib Impurity9
  • Lapatinib Impurity9
  • Lapatinib Impurity9
  • Lapatinib Impurity9
  • Lapatinib Impurity9

Lapatinib Impurity9 NEW

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

Product Details

Product Name: Lapatinib Impurity9 CAS No.: 202196-46-1
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/31
Molecular formula: C26H19N3O3

Lapatinib Impurity 9;202196-46-1

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

  • Product Number: L079009
    English Name: Lapatinib Impurity 9
    English Alias: 5-(4-((4-(benzyloxy)phenyl)amino)quinazolin-6-yl)furan-2-carbaldehyde
    CAS Number: 202196-46-1
    Molecular Formula: C??H??N?O?
    Molecular Weight: 421.45

  • Product Advantages: Lapatinib Impurity 9 has high purity and good chemical stability. Its structure is accurately confirmed by precise analytical methods such as nuclear magnetic resonance and mass spectrometry. Under different experimental conditions and storage environments, this impurity remains stable and uniform. As a reference substance, it can be used for accurate Lapatinib impurity analysis, ensuring the accuracy and repeatability of detection results, and providing a reliable basis for pharmaceutical quality control and research.

  • Application Fields:

  • Quality Control: As an impurity reference standard, it is used to establish and validate the detection methods for impurities in Lapatinib bulk drugs and formulations, ensuring that the sensitivity and specificity of the detection methods meet pharmaceutical quality standards and guaranteeing the consistency of drug quality.

  • Process Optimization: During the production of Lapatinib, by monitoring the content of this impurity and analyzing the reaction steps that generate it, it assists in optimizing the synthesis process, reducing impurity formation, and improving product quality and production efficiency.

  • Stability Studies: In drug stability tests, it studies the change rules of this impurity under different storage conditions (such as temperature, humidity, light), providing key data for determining the shelf life and storage conditions of drugs.


  • Background Description: Lapatinib is an important targeted drug for the treatment of HER2-positive breast cancer. In the process of its research, development, production, and quality control, impurity research is a key link to ensure drug safety and effectiveness. The presence of impurities may affect the activity, safety, and stability of the drug. As a related impurity of Lapatinib, in-depth research on Lapatinib Impurity 9 helps to comprehensively evaluate the quality of Lapatinib drugs and ensure the safety of patients' medication and the therapeutic effect.

  • Research Status: Currently, research on Lapatinib Impurity 9 mainly focuses on the development of detection technology and the exploration of impurity generation mechanisms. In terms of detection technology, advanced methods such as Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS/MS) and high-resolution mass spectrometry are constantly being explored to achieve precise detection of trace impurities. In the study of impurity generation mechanisms, the causes and influencing factors of its formation are analyzed by simulating drug synthesis reactions and storage environments, providing theoretical support for optimizing the production process and controlling impurity generation. At the same time, research on the impact of this impurity on the efficacy and safety of Lapatinib is also gradually being carried out.

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! 




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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