Benvitimod Impurity 12;344396-18-5

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

• Product Number: B051012
  English Name: Benvitimod Impurity 12
  English Alias: (E)-2-isopropyl-1,3-dimethoxy-5-styrylbenzene
  CAS Number: 141509-20-8
  Molecular Formula: C19H22O2
  Molecular Weight: 282.38
• 
  
• Product Advantages: Benvitimod Impurity 12 has extremely high purity and good chemical stability. Its structure is clear and properties are uniform, remaining stable under different experimental environments and storage conditions. It can be used as an accurate and reliable reference substance. In the process of pharmaceutical impurity analysis, it can effectively improve the accuracy and repeatability of detection results, providing strong support for in-depth research on the quality of Benvitimod drugs and strict quality control.
  Application Fields: It is mainly applied in the quality control and research and development of Benvitimod-related drugs. As an impurity reference standard, it is used to establish and validate the detection methods of Benvitimod impurities, ensuring that the detection methods have high sensitivity and strong specificity. During the drug production process, it monitors the content of this impurity in real-time, assists in optimizing the production process, and prevents excessive impurities from affecting drug quality. In the study of drug stability, it analyzes its change rules during storage, providing key basis for determining the shelf life and suitable storage conditions of drugs.
  Background Description: As an important drug for the treatment of skin diseases such as psoriasis, the quality of Benvitimod is directly related to clinical treatment effects and patients' medication safety. In the whole process of drug research and development, production and quality control, impurity research is an indispensable key part. The presence of impurities may interfere with the active ingredients of drugs, affect drug stability, and even bring potential toxic and side effects. As a related impurity of Benvitimod, in-depth research on Benvitimod Impurity 12 helps to comprehensively and accurately evaluate the quality of Benvitimod drugs, thereby ensuring the safety and effectiveness of clinical medication.
  Research Status: Currently, research on Benvitimod Impurity 12 is continuously deepening and expanding. In terms of detection technology, researchers are constantly exploring more advanced and efficient analytical methods, such as Ultra-Performance Liquid Chromatography - Mass Spectrometry (UPLC - MS) technology and high-resolution mass spectrometry technology, to achieve precise determination of trace impurities. In the study of impurity generation mechanisms, the root causes and influencing factors of its formation are deeply explored by simulating drug synthesis routes and storage environments, providing a solid theoretical basis for controlling impurities from the source. At the same time, research on the interaction between this impurity and Benvitimod and its impact on drug efficacy and safety is also gradually advancing, aiming to further improve the comprehensive cognitive system of Benvitimod drug 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 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!