Betaxolol impurity A EP Reference Standard - Reliable Reference Material

Betaxolol impurity A EP Reference Standard

CAS: 67193-95-7

Introducing Betaxolol impurity A EP Reference Standard, a high-quality product that serves as a reliable reference material for the identification, purity tests, and assays of pharmaceutical products according to European Pharmacopoeia (EP) monographs. With its exceptional composition and strict adherence to EP standards, this reference standard offers utmost confidence in the accuracy and reliability of your analytical results.

Product Details:

• Product Code: B1103100
• Chemical Name: Betaxolol impurity A
• Reference Standard Type: European Pharmacopoeia (EP)
• Chemical Formula: (1-(4-Ethylphenoxy)-3-(isopropylamino)propan-2-ol)
• CAS Number: 67193-95-7

Key Features and Benefits:

• Guaranteed Quality: Our Betaxolol impurity A EP Reference Standard is manufactured with utmost precision and adherence to EP standards, ensuring its reliability and accuracy.
• Authentication: Use this reference standard for the identification of Betaxolol impurity A in pharmaceutical products, providing a reliable benchmark to verify the presence and purity of this specific impurity.
• Purity Testing: With its well-characterized composition, this reference standard enables accurate purity testing, allowing you to assess the quality and purity of pharmaceutical products in accordance with EP requirements.
• Assays and Method Development: Incorporate this EP reference standard into your analytical methods and assays to ensure reliable and reproducible results. It serves as an essential tool for method development and validation in the pharmaceutical industry.
• EP Compliance: The Betaxolol impurity A EP Reference Standard strictly complies with the European Pharmacopoeia monographs, providing confidence in its suitability for use as a reference material for EP regulated products.
• Wide Application: This reference standard finds application in research, quality control, and regulatory activities involved in the development, manufacturing, and analysis of pharmaceutical products containing Betaxolol impurity A.

Product Usage:

Our Betaxolol impurity A EP Reference Standard is primarily used for identification, purity tests, and assays of pharmaceutical products according to the European Pharmacopoeia (EP) monographs. It serves as a reliable reference material for pharmaceutical laboratories, research institutions, and regulatory bodies involved in the development, testing, and analysis of pharmaceutical formulations containing Betaxolol impurity A.

Chemical Description:

Product Specifications:

• Appearance: White to off-white powder
• Purity (by HPLC): < 99% (sum of impurities < 1%)
• Identity (by NMR): Confirm as per EP monographs
• Molecular Weight: 295.41 g/mol
• Storage: Store at -20°C in a tightly sealed container, protected from light and moisture

Handling and Safety:

When handling Betaxolol impurity A EP Reference Standard, it is essential to follow proper laboratory safety practices, including the use of appropriate protective equipment. It is recommended to work in a well-ventilated area and avoid direct contact with skin, eyes, and clothing. In case of accidental exposure or ingestion, seek medical attention immediately and provide medical personnel with the necessary product information.

Refer to the provided Safety Data Sheet (SDS) for detailed handling instructions and safety precautions specific to Betaxolol impurity A EP Reference Standard.

Order your Betaxolol impurity A EP Reference Standard today and ensure the accuracy and reliability of your pharmaceutical product testing and analysis. With its guaranteed quality and EP compliance, this reference standard is an indispensable tool for pharmaceutical laboratories and regulatory bodies.