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Postion:Product Catalog >Carebastine Impurity9
Carebastine Impurity9
  • Carebastine Impurity9
  • Carebastine Impurity9
  • Carebastine Impurity9
  • Carebastine Impurity9
  • Carebastine Impurity9

Carebastine Impurity9 NEW

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

Product Details

Product Name: Carebastine Impurity9 Min. Order: 10mg
Purity: 99%+ HPLC Supply Ability: 1000
Release date: 2025/07/31

Carebastine Impurity

Article illustration


  • Product Number: C132009
  • English Name: Carebastine Impurity 9
  • English Alias: 2-(4-(4-(4-(benzhydryloxy)piperidin-1-yl)butanoyl)phenyl)propanoic acid
  • CAS Number: None
  • Molecular Formula: C31H35NO4
  • Molecular Weight: 485.61
  • Advantages: Carebastine Impurity 9 is synthesized through high-precision processes and strict purification methods, featuring high purity, strong stability, and minimal residual impurities. Its precise chemical structure has been verified through multiple rounds of testing, providing a reliable reference for drug research, development, and quality inspection, effectively reducing experimental deviations and ensuring the authenticity and validity of data.
  • Applications: It is mainly applied to the fields of impurity research, quality analysis, and control of Carebastine drugs. During the drug research and development process, it can be used to determine the content of this impurity in drugs and evaluate its potential impact on drug safety and effectiveness. In pharmaceutical production, as a key quality control reference standard, it can accurately detect impurities in products, helping enterprises strictly control drug quality and ensure compliance with domestic and international regulations and quality standards.
  • Background Description: With the high-quality development trend in the pharmaceutical industry, the research on drug impurities has become a core aspect of ensuring drug safety and efficacy. As a commonly used clinical drug, the control of impurities in Carebastine is directly related to patient medication safety and treatment outcomes. Carebastine Impurity 9, as one of the possible impurities in the drug, in-depth research on it helps to improve the drug quality control system and enhance the overall quality of drugs.
  • Research Status: Currently, research on Carebastine Impurity 9 is gradually unfolding. Researchers are actively exploring more sensitive and efficient detection methods, such as high-resolution mass spectrometry techniques, to achieve trace detection and precise quantification of this impurity. Meanwhile, studies on its origin during drug synthesis, interaction mechanisms with drug active ingredients, as well as its impact on drug stability and efficacy are also progressing continuously, aiming to provide solid theoretical and technical support for the research, development, production, and quality supervision of Carebastine drugs.

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


    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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