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Postion:Product Catalog >Flupentixol Impurity(Hydrochloride)
Flupentixol Impurity(Hydrochloride)
  • Flupentixol Impurity(Hydrochloride)
  • Flupentixol Impurity(Hydrochloride)
  • Flupentixol Impurity(Hydrochloride)
  • Flupentixol Impurity(Hydrochloride)
  • Flupentixol Impurity(Hydrochloride)

Flupentixol Impurity(Hydrochloride) NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-05-27

Product Details

Product Name: Flupentixol Impurity(Hydrochloride) Min. Order: 10mg
Purity: 99%+ HPLC Supply Ability: 1000
Release date: 2025/05/27

Flupentixol Impurity (Hydrochloride)

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

Product Information

    • Product Information

      • Product Number: F058021A

      • English Name: Flupentixol Impurity 21(Hydrochloride)

      • English Alias: (E)-2-(4-(3-(2-(trifluoromethyl)-9H-thioxanthen-9-ylidene)propyl)piperazin-1-yl)ethyl 4-chlorobenzoate hydrochloride

      • CAS Number: None

      • Molecular Formula: C30H28ClF3N2O2S.HCl

      • Molecular Weight: 609.53

    • Advantages: As a reference standard for Flupentixol Impurity 21 (hydrochloride), it has an accurate chemical structure and high purity, with strict quality control and identification. It has good stability and can maintain stable properties under different storage conditions and experimental environments. It can be used as a reliable reference substance for the impurity detection of flupentixol bulk drugs and formulations, ensuring the accuracy and repeatability of detection results, meeting the strict requirements of drug research, development, production, and quality supervision, and helping to precisely control drug quality.

    • Applications: It is mainly used in the quality research, impurity analysis, and quality control of flupentixol 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 flupentixol, 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 21 (hydrochloride) 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 flupentixol drugs during storage and transportation, providing data support for drug stability research.

    • Background Description: Flupentixol is a drug used for the treatment of mental 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 flupentixol are essential. As one of the impurities of flupentixol, in-depth research on Flupentixol Impurity 21(Hydrochloride) helps to improve the quality standard system of flupentixol, enhance drug quality, and ensure the safety and effectiveness of clinical medication.

    • Research Status: Currently, the research on Flupentixol Impurity 21(Hydrochloride) 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 flupentixol, 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 flupentixol drugs is also gradually underway, aiming to provide a more comprehensive scientific basis for the overall evaluation of flupentixol 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! 



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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