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Vildagliptin Impurity 17

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For Research Use Only | Not For Clinical Use
CATAPB1616662840
CAS1616662-84-0
Molecular Weight268.32
Molecular FormulaC12H20N4O3

What is the chemical name for CAS 1616662-84-0?

The chemical name for CAS 1616662-84-0 is Vildagliptin Impurity 17.

What is the molecular weight of Vildagliptin Impurity 17?

The molecular weight of Vildagliptin Impurity 17 is 268.32.

What is the molecular formula of Vildagliptin Impurity 17?

The molecular formula of Vildagliptin Impurity 17 is C12H20N4O3.

What is the structure of Vildagliptin Impurity 17 based on its molecular formula?

The structure of Vildagliptin Impurity 17 based on its molecular formula consists of 12 carbon atoms, 20 hydrogen atoms, 4 nitrogen atoms, and 3 oxygen atoms.

What are the potential impurities of Vildagliptin Impurity 17?

The potential impurities of Vildagliptin Impurity 17 may include related substances or degradation products that could be present in the sample.

How is Vildagliptin Impurity 17 typically characterized in analytical chemistry?

Vildagliptin Impurity 17 is typically characterized in analytical chemistry using techniques such as mass spectrometry, nuclear magnetic resonance (NMR) spectroscopy, and chromatography.

Why is it important to identify and quantify impurities like Vildagliptin Impurity 17 in pharmaceutical products?

Identifying and quantifying impurities like Vildagliptin Impurity 17 in pharmaceutical products is important to ensure the safety, efficacy, and quality of the medication for patient use.

What are some methods that can be used to separate Vildagliptin Impurity 17 from the main pharmaceutical ingredient?

Methods such as crystallization, chromatography, and recrystallization can be used to separate Vildagliptin Impurity 17 from the main pharmaceutical ingredient.

Are there regulatory guidelines in place regarding the acceptable levels of impurities like Vildagliptin Impurity 17 in pharmaceutical products?

Yes, regulatory agencies like the FDA and EMA have established guidelines for the acceptable levels of impurities, including Vildagliptin Impurity 17, in pharmaceutical products.

How can manufacturers ensure that pharmaceutical products meet the regulatory standards for impurities like Vildagliptin Impurity 17?

Manufacturers can ensure that pharmaceutical products meet the regulatory standards for impurities by conducting thorough analytical testing, implementing quality control measures, and following Good Manufacturing Practices (GMP).

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