Keywords

• 72810-61-8
• 4-(m-tolyl)-2H-pyrido[4,3-e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxide
• Torsemide Impurity A

Quick Details

• ProName: Torsemide Impurity A
• CasNo: 72810-61-8
• Molecular Formula: C13H11N3O3S
• Appearance: solid
• Application: for drug impurity for drug standards,f...
• DeliveryTime: 1-2 weeks
• PackAge: 10mg/25mg/50mg/100mg/1000mg/5000mg
• Port: SHENZHEN or SHANGHAI
• ProductionCapacity: 5000 Metric Ton/Year
• Purity: 95%+ or 98%+
• Storage: short-term storage normal temperature....
• Transportation: express and sea transport and air frei...
• LimitNum: 25 Milligram
• Moisture Content: within 3%
• Impurity: within 5%

Superiority

• 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.

Our products are mainly drug impurity reference products, drug standards, analytical chemistry, standard substances, organic chemical synthesis, chemical custom synthesis. For impurity localization, quantification, and quality control in drug development processes. Our laboratory area is more than 5000 square meters, we have more than 20 analytical instruments such as HPLC and MS/LC-MS/GC-MS, we also have TGA, IR and other testing instruments. We have the most advanced SFC preparation separation equipment. We can provide a full range of impurity reference/standard products required for drug development. Most of the impurities are synthesized through the process, there are also many items of impurities can not be obtained by synthetic means, need to be obtained through raw materials, intermediates, crude products or side reactions contained in the trace target compounds, Hubei Moke has a professional impurity preparation and separation technology team, equipped with professional SFC preparation and separation equipment. It can carry out efficient and accurate separation of impurities for complex projects, and solve the problem of impurity preparation for customers.

1. We integrate R&D, production and sales. A 5,000-square-meter high-standard bio-intelligent manufacturing base can ensure high quality and fast delivery of products. The professional sales team ensures that you don't need to worry about pre-sales and after-sales.

2. We focus on pharmaceutical standards, pharmaceutical intermediates, pharmaceutical impurity controls, peptide customization, our own laboratory, and undertake customized synthesis projects.

3. We offer products from gram grade to g grade, in addition, some product specifications and packaging can be customized.

4. We have been deeply engaged in the pharmaceutical field for ten years and have rich experience. At present, customers are all over the world, and have been highly recognized and trusted by customers.

5. We can provide a variety of safe ways to transport goods for you to choose.

Details

Torsemide Impurity A72810-61-8

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.

All of our products include a complete set of structural confirmation maps. Such as COA, H-NMR,MASS,HPLC,UV,IR。The default HPLC purity of our products is not less than 95%. Particularly unstable products have a purity of no less than 90% and will be communicated to the customer in advance. we can also provide TGA,Q-NMR,C-NMR and so on。
Our testing and analysis laboratory is equipped with a variety of foreign imported testing equipment such as LC-MS, liquid phase, TGA, infrared, etc., to escort research and development.
At the same time, it also provides customers with faster, more true and accurate product quality confirmation.
For impurities with different properties, Moco provides accurate impurity adaptation environment (-80°C, -20°C, 2-8°C), and uses different adapted reagent bottles to ensure the stable storage of impurity controls in various environments.