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Postion:Product Catalog >Analytical Chemistry>Standard>Pharmaceutical Impurity Reference Standards>Torsemide Impurity A
Torsemide Impurity A
  • Torsemide Impurity A
  • Torsemide Impurity A
  • Torsemide Impurity A
  • Torsemide Impurity A
  • Torsemide Impurity A

Torsemide Impurity A NEW

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

Product Details

Product Name: Torsemide Impurity A CAS No.: 72810-61-8
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/31

Torsemide Impurity A72810-61-8

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

Product Information

    • Product Information

      • Product Number: T042001

      • English Name: Torsemide Impurity A

      • English Alias: 4-(m-tolyl)-2H-pyrido[4,3-e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxide

      • CAS Number: 72810-61-8

      • Molecular Formula: C13H11N3O3S

      • Molecular Weight: 289.31

    • Advantages: As a reference standard for Torsemide Impurity A, it has a clear chemical structure, and its purity has been strictly determined and verified. It has good stability and uniformity. In the process of drug quality testing, it can be used as a reliable reference substance to ensure the accuracy and repeatability of the detection results of Impurity A in torsemide bulk drugs and formulations, providing strong support for quality control in the drug research and production process, and meeting the strict requirements of drug regulation for impurity research.

    • Applications: It is mainly used in the quality research, impurity analysis, and quality control of torsemide bulk drugs and formulations. It is used to establish and validate impurity detection methods such as high-performance liquid chromatography (HPLC) and liquid chromatography - mass spectrometry (LC - MS). In the research and development process of torsemide, it helps to study the source and formation mechanism of this impurity, so as to optimize the synthesis process and reduce impurity generation. In the production process, it is used to monitor the content of Torsemide Impurity A in products in real time to ensure that drug quality meets relevant standards and regulatory requirements. It can also be used to evaluate the changes of impurities in torsemide drugs during storage and transportation, providing data support for drug stability research.

    • Background Description: Torsemide is a highly effective loop diuretic commonly used in the treatment of heart failure, edema, and other conditions. In the process of its production and research and development, the presence of impurities may affect the safety, effectiveness, and stability of the drug. To ensure the safety of patients' medication and meet the requirements of drug regulation, strict research and precise control of various impurities in torsemide are essential. As one of the important impurities of torsemide, in-depth research on Torsemide Impurity A helps to improve the quality standard system of torsemide, enhance drug quality, and ensure the safety and effectiveness of clinical medication.

    • Research Status: Currently, the research on Torsemide Impurity A mainly focuses on the optimization and improvement of impurity analysis methods. By using more advanced detection technologies and instruments, the sensitivity and accuracy of detecting this impurity are improved to achieve precise determination of trace impurities. At the same time, researchers are actively exploring the source and change rules of this impurity during the synthesis and storage of torsemide, and reducing the generation and accumulation of impurities by improving process conditions and optimizing the storage environment. In addition, the research on the potential impact of this impurity on the performance and safety of torsemide drugs is also gradually underway, aiming to provide a more comprehensive scientific basis for the overall evaluation of torsemide 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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