Vildagliptin Impurity 28

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For Research Use Only | Not For Clinical Use

CAT	APB16104282
CAS	16104-28-2
Molecular Weight	200.23
Molecular Formula	C10H16O4

What is the product name of the compound with CAS number 16104-28-2?

The product name is Vildagliptin Impurity 28.

What is the molecular weight of Vildagliptin Impurity 28?

The molecular weight is 200.23.

What is the molecular formula of Vildagliptin Impurity 28?

The molecular formula is C10H16O4.

What is the chemical structure of Vildagliptin Impurity 28 based on its molecular formula?

The chemical structure of Vildagliptin Impurity 28 is comprised of 10 carbon atoms, 16 hydrogen atoms, and 4 oxygen atoms.

What is the significance of an impurity in a pharmaceutical compound like Vildagliptin?

Impurities in pharmaceutical compounds like Vildagliptin can affect the efficacy and safety of the drug, hence it is important to identify and characterize them.

How is Vildagliptin Impurity 28 typically characterized in a laboratory setting?

Vildagliptin Impurity 28 is typically characterized using techniques such as spectroscopy, chromatography, and mass spectrometry.

Why is it necessary to accurately identify and quantify impurities in pharmaceutical products like Vildagliptin?

Accurately identifying and quantifying impurities in pharmaceutical products is crucial for ensuring product quality, safety, and efficacy.

How can the presence of impurities like Vildagliptin Impurity 28 impact the shelf life of a pharmaceutical product?

The presence of impurities can degrade over time, leading to changes in the chemical composition of the product and potentially reducing its shelf life.

What are some potential sources of impurities in pharmaceutical products like Vildagliptin?

Impurities can originate from raw materials, the manufacturing process, storage conditions, and even interactions with packaging materials.

How can regulatory agencies like the FDA regulate the limits of impurities in pharmaceutical products like Vildagliptin?

Regulatory agencies establish guidelines and standards for acceptable levels of impurities in pharmaceutical products, which manufacturers must adhere to in order to market their products legally.

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