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Postion:Product Catalog >Difelikefalin Impurity 22
Difelikefalin Impurity 22
  • Difelikefalin Impurity 22
  • Difelikefalin Impurity 22
  • Difelikefalin Impurity 22
  • Difelikefalin Impurity 22
  • Difelikefalin Impurity 22

Difelikefalin Impurity 22 NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-06-28

Product Details

Product Name: Difelikefalin Impurity 22 CAS No.: 2219351-85-4
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/06/28
Molecular formula: C24H31N3O4

Difelikefalin Impurity 22;2219351-85-4

Article illustration

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


  • Product Number: D079022
    English Name: Difelikefalin Impurity 22
    English Alias: (R)-2-((R)-2-((R)-2-amino-3-phenylpropanamido)-3-phenylpropanamido)-4-methylpentanoic acid
    CAS Number: 2219351-85-4
    Molecular Formula: C??H??N?O?
    Molecular Weight: 425.52

  • Product Advantages: Difelikefalin Impurity 22 has high purity and good chemical stability. Its structure is confirmed by precise spectroscopic analysis (such as nuclear magnetic resonance and mass spectrometry), and it remains stable and uniform under different experimental conditions. As a reference substance, its precision ensures the accuracy and repeatability of Difelikefalin impurity detection results, providing a reliable basis for pharmaceutical quality control and facilitating quality research in the drug research and development and production processes.

  • Application Fields:

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

  • Process Optimization: During the production of Difelikefalin, by monitoring the content of this impurity and analyzing the stages of its generation, it assists in optimizing the synthesis process, reducing impurity formation, and improving product quality.

  • Stability Studies: In drug stability tests, it analyzes the changes of this impurity under different storage conditions, providing data support for determining the shelf life and storage conditions of drugs.


  • Background Description: Difelikefalin is a drug used for the treatment of pruritus associated with chronic kidney disease. 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 drug's efficacy and even bring potential toxic and side effects. As a related impurity of Difelikefalin, in-depth research on Difelikefalin Impurity 22 helps to comprehensively evaluate the quality of Difelikefalin drugs and ensure the safety of clinical medication.

  • Research Status: Currently, research on Difelikefalin Impurity 22 mainly focuses on detection technology and 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 a theoretical basis for controlling impurities from the source. In addition, research on the impact of this impurity on the efficacy and safety of Difelikefalin 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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