Dotinurad Impurity NEW

Dotinurad Impurity

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

Product Information

• Product Information

• Product Number: D081067

• English Name: Dotinurad Impurity 67

• English Alias: (1,1 - dioxidobenzo[d]thiazol-3(2H)-yl)methanesulfonic acid

• CAS Number: None

• Molecular Formula: C8H9NO5S2

• Molecular Weight: 263.29

• Advantages: As a reference standard for Dotinurad Impurity 67, it has an accurate and clear chemical structure, and has undergone strict purity determination and quality control, with good stability under different storage conditions. It can provide a reliable reference for the quality inspection of dotinurad bulk drugs and formulations, ensuring the accuracy and repeatability of impurity detection results. It helps pharmaceutical companies and research institutions to effectively carry out quality control in the process of drug research and development and production, meeting the high standards of drug regulation.

• Applications: It is mainly used in the quality research and control of dotinurad 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 dotinurad, it is used to study the source and formation mechanism of this impurity, and optimize the synthesis process to reduce impurity generation. In the production process, it is used to monitor the content of Impurity 67 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 dotinurad drugs during storage and transportation, providing data support for drug stability research.

• Background Description: Dotinurad is a drug used for the treatment of urinary system diseases. In the process of its research and development and production, 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 impurities in dotinurad are essential. As one of the impurities of dotinurad, in-depth research on Dotinurad Impurity 67 helps to improve the quality standard system of dotinurad, enhance drug quality, and ensure the safety and effectiveness of clinical medication.

• Research Status: Currently, the research on Dotinurad Impurity 67 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 dotinurad, 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 dotinurad drugs is also gradually underway, aiming to provide a more comprehensive scientific basis for the overall evaluation of dotinurad 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!