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Postion:Product Catalog >Organic Chemistry>Alcohols,Phenols,Phenol alcohols>Benvitimod Impurity 9
Benvitimod Impurity 9
  • Benvitimod Impurity 9
  • Benvitimod Impurity 9
  • Benvitimod Impurity 9
  • Benvitimod Impurity 9
  • Benvitimod Impurity 9

Benvitimod Impurity 9 NEW

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Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-06-28

Product Details

Product Name: Benvitimod Impurity 9 CAS No.: 344396-18-5
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/06/28
Molecular formula: C16H27O5P

Benvitimod Impurity 9;344396-18-5

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


  • Product Number: B051009
    English Name: Benvitimod Impurity 9
    English Alias: (4-isopropyl-3,5-dimethoxyphenyl)methanol
    CAS Number: 344396-18-5
    Molecular Formula: C12H18O3
    Molecular Weight: 210.27

  • Product Advantages: Benvitimod Impurity 9 has high purity and good chemical stability. With a clear structure and uniform properties, it can remain stable under different experimental conditions. It can be used as a reliable reference substance for Benvitimod impurity analysis. Its precise characteristics can ensure the accuracy and repeatability of detection results, providing strong support for pharmaceutical quality research and quality control.
    Application Fields: It is mainly applied in the quality control and research and development process of Benvitimod - related drugs. As an impurity reference standard, it is used to establish and validate the detection methods of Benvitimod impurities, ensuring the sensitivity and specificity of detection methods. During the drug production process, it monitors the content of this impurity, assists in optimizing the production process, and prevents excessive impurities from affecting drug quality. In the study of drug stability, it analyzes its changes during storage, providing important basis for determining the shelf life and storage conditions of drugs.
    Background Description: Benvitimod is a drug used to treat skin diseases such as psoriasis. During the process of its research, development, production and quality control, impurity research is of great importance. The presence of impurities may affect the safety and effectiveness of drugs. As a related impurity of Benvitimod, in - depth research on Benvitimod Impurity 9 helps to comprehensively evaluate the quality of Benvitimod drugs and ensure the safety of clinical medication and treatment effects.
    Research Status: Currently, research on Benvitimod Impurity 9 continues to advance. In terms of detection technology, more advanced analytical methods are constantly being explored and optimized, such as Ultra - Performance Liquid Chromatography - Mass Spectrometry (UPLC - MS) and high - resolution mass spectrometry, to achieve accurate detection of trace impurities. In the study of impurity generation mechanisms, the formation causes and influencing factors are deeply analyzed by simulating the drug synthesis process and storage environment, providing theoretical support 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 carried out, aiming to further improve the comprehensive understanding of the quality of Benvitimod drugs.

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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