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Pramipexole EP Impurity F

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For Research Use Only | Not For Clinical Use
CATAPB104617767
CAS104617-76-7
Molecular Weight253.41
Molecular FormulaC13H23N3S

What is the product name of the impurity with CAS number 104617-76-7?

The product name is Pramipexole EP Impurity F.

What is the molecular weight of Pramipexole EP Impurity F?

The molecular weight is 253.41.

What is the molecular formula of Pramipexole EP Impurity F?

The molecular formula is C13H23N3S.

What is the chemical structure of Pramipexole EP Impurity F?

The chemical structure is composed of 13 carbon atoms, 23 hydrogen atoms, 3 nitrogen atoms, and 1 sulfur atom.

How is Pramipexole EP Impurity F related to the drug Pramipexole?

Pramipexole EP Impurity F is an impurity associated with the drug Pramipexole.

What is the significance of identifying impurity F in Pramipexole?

Identifying impurity F in Pramipexole is important for quality control and ensuring the potency and safety of the drug.

What are the potential effects of impurity F on the efficacy of Pramipexole?

Impurity F may affect the efficacy of Pramipexole by altering its pharmacological properties or causing adverse reactions in patients.

How is Pramipexole EP Impurity F typically detected and quantified in pharmaceutical products?

Pramipexole EP Impurity F is typically detected and quantified using analytical techniques such as chromatography or spectroscopy.

What steps can be taken to minimize the presence of impurity F in Pramipexole formulations?

Manufacturers can implement strict quality control measures and purification processes to minimize the presence of impurity F in Pramipexole formulations.

Are there any specific regulations or guidelines regarding the acceptable levels of impurities in pharmaceutical products like Pramipexole?

Yes, regulatory authorities often have guidelines on the acceptable levels of impurities in pharmaceutical products to ensure patient safety and product quality.

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