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Postion:Product Catalog >rac-Domperidone EP Impurity C
rac-Domperidone EP Impurity C
  • rac-Domperidone EP Impurity C
  • rac-Domperidone EP Impurity C
  • rac-Domperidone EP Impurity C
  • rac-Domperidone EP Impurity C
  • rac-Domperidone EP Impurity C

rac-Domperidone EP Impurity C NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-07-02

Product Details

Product Name: rac-Domperidone EP Impurity C CAS No.: 118435-03-3
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/02
Molecular formula: C22H24ClN5O3

rac-Domperidone EP Impurity C;118435-03-3

Article illustration

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

  • Product Information

  • Product Number: D028005

  • English Name: rac-Domperidone EP Impurity C

  • English Alias: Domperidone N-Oxide; 4-(5-chloro-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)-1-(3-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)propyl)piperidine 1-oxide

  • CAS Number: 118435-03-3

  • Molecular Formula: C??H??ClN?O?

  • Molecular Weight: 441.91

  • Advantages

  • As a European Pharmacopoeia (EP) standard impurity of domperidone, this compound has the following advantages:

  • Well-defined structure compliant with EP standards, directly applicable to quality testing of domperidone APIs and formulations to ensure consistency with international pharmacopoeia requirements;

  • As an N-oxide impurity, it can be used to analyze the by-product formation mechanism of oxidation reactions during domperidone synthesis or storage, optimizing processes to control N-oxide impurity generation;

  • Helps study the impact of N-oxide structures on drug stability and safety (N-oxides may have different pharmacological activities or toxicities) to provide a scientific basis for impurity control strategies.

  • Applications

  • Quality Control: Used as an EP standard impurity reference for system suitability tests in HPLC and other detection methods to verify whether the content of this impurity in domperidone meets EP limits;

  • Drug Development: In generic drug research, used to compare the impurity profile of the original drug to ensure quality consistency between the generic and original drug;

  • Stability Studies: Investigating the formation rate of this impurity under light and high-temperature conditions to evaluate its impact on domperidone formulation stability and assist in establishing storage conditions.

  • Background Description

  • Domperidone is a dopamine receptor antagonist clinically used for treating dyspepsia, nausea, and vomiting. The piperidine nitrogen atom in its molecular structure is prone to oxidation reactions in the presence of oxidants or during storage, generating N-oxide impurities (such as Impurity C). The European Pharmacopoeia (EP) has clear limits for this impurity, making research on it a necessary part of international quality control for domperidone.
  • Research Status

  • Current research focuses on:

  • Detection Method Optimization: Using EP-recommended HPLC-UV or LC-MS combined techniques to improve the detection sensitivity and specificity of this impurity;

  • Synthesis Process Improvement: Reducing N-oxide by-product generation by adjusting antioxidant conditions in the reaction system (such as inert gas protection, antioxidant addition);

  • Toxicological Evaluation: Studying the potential toxicity of N-oxide structures through in vitro cell experiments to provide data support for establishing safe limits;

  • Stability Prediction: Establishing a formation kinetics model for this impurity based on accelerated test data to predict the shelf life of domperidone formulations.

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





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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