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Vilanterol Impurity 20

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For Research Use Only | Not For Clinical Use
CATAPB10026
Molecular Weight249.27
Molecular FormulaC13H15NO4

What is the molecular weight of Vilanterol Impurity 20?

The molecular weight of Vilanterol Impurity 20 is 249.27.

What is the molecular formula of Vilanterol Impurity 20?

The molecular formula of Vilanterol Impurity 20 is C13H15NO4.

What is the chemical structure of Vilanterol Impurity 20?

The chemical structure of Vilanterol Impurity 20 is C13H15NO4.

How does Vilanterol Impurity 20 differ from the main compound Vilanterol?

Vilanterol Impurity 20 is an impurity of Vilanterol, meaning it is a compound that is present in Vilanterol as an unintended byproduct.

What is the significance of identifying Vilanterol Impurity 20 in a sample?

Identifying Vilanterol Impurity 20 in a sample is important for quality control purposes to ensure the purity and efficacy of the Vilanterol product.

How is Vilanterol Impurity 20 detected and quantified in pharmaceutical samples?

Vilanterol Impurity 20 can be detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry.

What are the potential risks of having Vilanterol Impurity 20 in a pharmaceutical product?

Vilanterol Impurity 20 may pose health risks or affect the efficacy of the drug if present in high concentrations.

Are there regulations or guidelines regarding the acceptable levels of Vilanterol Impurity 20 in pharmaceutical products?

Yes, regulatory authorities often have specific limits on impurities like Vilanterol Impurity 20 in pharmaceutical products.

How can the presence of Vilanterol Impurity 20 be minimized during the manufacturing process?

Manufacturers may implement quality control measures and purification techniques to minimize the presence of Vilanterol Impurity 20 in the final product.

Are there any known interactions or side effects associated with Vilanterol Impurity 20?

The specific interactions or side effects of Vilanterol Impurity 20 would depend on its concentration and the individual's response to the impurity, but generally impurities may affect the overall safety and effectiveness of the drug.

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