Nifedipine USP Reference Standard - High-Quality Product for Thermal Analytical Tests

Nifedipine USP Reference Standard

The Nifedipine USP Reference Standard is a high-quality product that is widely used as a reference standard for thermal analytical tests during the demonstration of nifedipine tablets using thermogravimetry. It is a valuable tool for researchers, scientists, and pharmaceutical companies involved in the development and quality control of nifedipine-based medications.

With a CAS number of 21829-25-4, the Nifedipine USP Reference Standard is composed of Nifedipine - 1, 4-Dihydro-2, 6-dimethyl-4-(2-nitrophenyl)-3, 5-pyridinedicarboxylic acid dimethyl ester. This compound is a yellow crystalline powder that is insoluble in water but soluble in organic solvents such as acetone and methanol.

Key Features:

• High purity: The reference standard is of high purity, ensuring accurate and reliable results in analytical tests.
• Consistent composition: The composition of the reference standard is consistent from batch to batch, allowing for reproducibility of experiments and reliable comparisons.
• Stability: The Nifedipine USP Reference Standard is stable under recommended storage conditions, ensuring a long shelf life.
• Easy to use: The reference standard is conveniently packaged and comes with clear instructions for use, making it user-friendly for researchers and scientists.

Applications:

The Nifedipine USP Reference Standard is primarily used as a reference material for thermal analytical tests during the demonstration of nifedipine tablets using thermogravimetry. By using the Nifedipine USP Reference Standard as a benchmark, pharmaceutical companies can ensure the accuracy and reliability of their thermogravimetry measurements, ultimately leading to improved quality control in the production of nifedipine tablets.

Storage and Handling:

It is important to store the Nifedipine USP Reference Standard in a cool, dry place away from direct sunlight. The product should be kept in its original packaging and properly sealed to prevent contamination and moisture absorption. When handling the reference standard, it is recommended to use appropriate personal protective equipment, including gloves and goggles, to ensure safety.

Molecular Structure:

The Nifedipine USP Reference Standard has a complex molecular structure, consisting of a 1, 4-Dihydro-2, 6-dimethyl-4-(2-nitrophenyl)-3, 5-pyridinedicarboxylic acid dimethyl ester backbone. This structure enables the compound to exhibit specific chemical and physical properties that make it suitable for use as a reference standard in thermal analytical tests.

Quality Assurance:

The Nifedipine USP Reference Standard is manufactured in accordance with strict quality control guidelines to ensure its purity, consistency, and reliability. The product undergoes rigorous testing and analysis to meet the highest standards of quality. The batch-specific certificate of analysis provides detailed information on the quality and composition of the reference standard, including purity, impurity levels, and physical properties.

At every stage of the manufacturing process, from raw material sourcing to final packaging, quality checks and controls are implemented to guarantee the integrity of the product. This commitment to quality assurance ensures that researchers and scientists can rely on the Nifedipine USP Reference Standard for accurate and reproducible results in their analytical tests.

Conclusion:

The Nifedipine USP Reference Standard is a high-quality product widely used as a benchmark for thermal analytical tests during the demonstration of nifedipine tablets using thermogravimetry. With its high purity, consistent composition, and stability, this reference standard provides researchers and scientists with the confidence to achieve accurate and reliable results in their work. When it comes to quality control and research in the field of nifedipine-based medications, the Nifedipine USP Reference Standard is an essential tool.