Milrinone Impurity 12

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For Research Use Only | Not For Clinical Use

CAT	APB80047387
CAS	80047-38-7
Molecular Weight	230.22
Molecular Formula	C12H10N2O3

What is the product name of the chemical with CAS number 80047-38-7?

The product name is Milrinone Impurity 12.

What is the molecular weight of Milrinone Impurity 12?

The molecular weight is 230.22.

What is the molecular formula of Milrinone Impurity 12?

The molecular formula is C12H10N2O3.

What is the chemical structure of Milrinone Impurity 12 based on its molecular formula?

The chemical structure would consist of 12 carbon atoms, 10 hydrogen atoms, 2 nitrogen atoms, and 3 oxygen atoms arranged in a specific configuration.

What is the significance of the presence of impurities in the pharmaceutical compound Milrinone?

Impurities in pharmaceutical compounds like Milrinone can affect the efficacy, safety, and quality of the product, which is why it is important to identify and characterize them.

How is Milrinone Impurity 12 typically identified and characterized in pharmaceutical research and development?

Milrinone Impurity 12 is usually identified and characterized through various analytical techniques such as spectroscopy, chromatography, and mass spectrometry.

Why is it important for pharmaceutical manufacturers to control the levels of impurities like Milrinone Impurity 12 in their products?

Controlling impurity levels ensures that the pharmaceutical product meets quality standards, regulatory requirements, and is safe for patient use.

Can the presence of impurities like Milrinone Impurity 12 affect the shelf-life or stability of a pharmaceutical product?

Yes, impurities can impact the shelf-life and stability of a pharmaceutical product, leading to degradation or changes in its effectiveness over time.

Are there specific guidelines or regulations set by authorities regarding the permissible levels of impurities in pharmaceutical products like Milrinone?

Yes, regulatory bodies like the FDA and EMA have guidelines on impurity levels in pharmaceuticals to ensure product safety and quality.

How can pharmaceutical companies mitigate the presence of impurities like Milrinone Impurity 12 during drug development and manufacturing processes?

Pharmaceutical companies can implement rigorous quality control measures, conduct thorough impurity profiling studies, and use advanced purification techniques to minimize impurities in their products.

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