Fluorouracil Impurity F EP Reference Standard - High-Quality Pharmaceutical Analytical Tool

Fluorouracil Impurity F EP Reference Standard

The Fluorouracil Impurity F EP Reference Standard is a high-quality product used for identification, purity tests, and assays of pharmaceutical products, in accordance with the European Pharmacopoeia (EP) monographs. This reference standard is essential for ensuring the reliability and accuracy of pharmaceutical analyses and assays.

Main Features:

• Chemical Name: 5-Fluoro-2-ethoxy-4(1H)pyrimidinone
• Alternate Name: 2-Ethoxy-5-fluoropyrimidin-4(1H)-one
• CAS Number: 56177-80-1
• Molecular Formula: C4N2H2FOOCH2CH3

Detailed Description:

The Fluorouracil Impurity F EP Reference Standard is a highly pure and authentic substance that is widely used in the pharmaceutical industry for various applications. This reference standard is intended for use in analytical laboratories, research and development, and quality control departments to ensure the identity, purity, and reliability of pharmaceutical products. It is specifically designed to meet the requirements set forth in the EP monographs, making it an essential tool for pharmaceutical analysis.

The chemical name of this reference standard is 5-Fluoro-2-ethoxy-4(1H)pyrimidinone, with an alternate name of 2-Ethoxy-5-fluoropyrimidin-4(1H)-one. It is identified by the CAS number 56177-80-1, enabling easy identification and traceability. The molecular formula of this compound is C4N2H2FOOCH2CH3, providing valuable information about its composition and structure.

The Fluorouracil Impurity F EP Reference Standard is manufactured with utmost precision and adherence to stringent quality standards. It undergoes rigorous testing and analysis to ensure its purity, authenticity, and stability. The use of this reference standard enables accurate and reproducible analysis of pharmaceutical products, ensuring that they meet the required specifications and standards.

As a reference standard, the Fluorouracil Impurity F EP Reference Standard provides several advantages and benefits for pharmaceutical analysis and quality control. These include:

• Facilitates identification: The reference standard simplifies the identification process by providing a well-defined and authentic sample with known properties and characteristics.
• Ensures accuracy of analyses: By using the reference standard, analysts can compare the properties, behaviors, and analytical results of pharmaceutical products against a known standard, ensuring accuracy and reliability in their analyses.
• Verifies purity: The Fluorouracil Impurity F EP Reference Standard is crucial for purity tests, as it serves as a benchmark for determining impurities and their levels in pharmaceutical products.
• Complies with EP monographs: This reference standard is specifically manufactured and tested to meet the requirements set forth in the EP monographs, ensuring its suitability and compatibility with EP-compliant analyses.
• Promotes quality control: Pharmaceutical manufacturers can use the reference standard to establish and maintain quality control protocols, ensuring consistency, reliability, and compliance with regulatory standards.

In conclusion, the Fluorouracil Impurity F EP Reference Standard is a highly reliable and essential tool for pharmaceutical analysis and quality control. With its well-defined properties, known composition, and adherence to EP monographs, it ensures accuracy, reliability, and compliance in the analysis and assays of pharmaceutical products. By using this reference standard, pharmaceutical manufacturers, researchers, and analysts can confidently assess the quality, purity, and compliance of their products, contributing to the overall safety and effectiveness of pharmaceuticals in the market.