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Postion:Product Catalog >Darunavir Impurity 4
Darunavir Impurity 4
  • Darunavir Impurity 4
  • Darunavir Impurity 4
  • Darunavir Impurity 4
  • Darunavir Impurity 4
  • Darunavir Impurity 4

Darunavir Impurity 4 NEW

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

Product Details

Product Name: Darunavir Impurity 4 CAS No.: 1291087-81-4
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/31
Molecular formula: C34H45N3O11S

Darunavir Impurity 4;1291087-81-4

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

  • Product Information

  • Product Code: D034004

  • English Name: Darunavir Impurity 4

  • English Alias: (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl ((2S,3R)-4-(4-amino-N-isobutylphenylsulfonamido)-3-(((((3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl)oxy)carbonyl)oxy)-1-phenylbutan-2-yl)carbamate

  • CAS No.:1291087-81-4

  • Molecular Formula: C??H??N?O??S

  • Molecular Weight: 703.80

  • Advantages

  • As an important impurity of Darunavir, this compound features a clear structure and controllable purity. It is applicable for the qualitative and quantitative analysis of impurities in the drug research and development process, ensuring the quality, safety, and consistency of the main drug, and providing key references for pharmaceutical quality control.
  • Applications

  • It is mainly used in the research, quality study, and stability investigation of Darunavir-related drugs. As a reference standard, it can be used for the establishment and validation of detection methods such as chromatographic analysis (e.g., HPLC, LC-MS) and spectral analysis. It can also be used to evaluate the generation and control level of impurities in the pharmaceutical production process.
  • Background Description

  • Darunavir is a protease inhibitor used in the treatment of human immunodeficiency virus (HIV) infection, with wide clinical application. The generation of impurities is inevitable during drug synthesis and storage, and the presence of impurities may affect the efficacy and safety of the drug. Therefore, the study of Darunavir impurities is an important part of the drug quality control system. The research on the structure and properties of Darunavir Impurity 4, as a specific impurity, is of great significance for ensuring drug quality.
  • Research Status

  • At present, the research on this impurity mainly focuses on the development of analytical methods, toxicity assessment, and optimization of synthetic routes. Researchers have established quantitative analytical methods for this impurity through efficient separation technologies and precise detection means. Meanwhile, by simulating the drug production process, the formation mechanism of this impurity is explored to optimize the production process and reduce its generation. In addition, the interaction between this impurity and the main drug and its potential impact on drug efficacy are also under further study.

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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