Pramipexole Impurity 21

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For Research Use Only | Not For Clinical Use

What is the product name of the compound with CAS number 104617-86-9?

The product name is Pramipexole Impurity 21.

What is the molecular weight of Pramipexole Impurity 21?

The molecular weight is 211.33.

What is the molecular formula of Pramipexole Impurity 21?

The molecular formula is C10H17N3S.

What is the chemical structure of Pramipexole Impurity 21 based on its molecular formula?

The chemical structure contains 10 carbon atoms, 17 hydrogen atoms, 3 nitrogen atoms, and 1 sulfur atom.

What is the significance of Pramipexole Impurity 21 in pharmaceutical research?

It is an impurity of the drug Pramipexole that needs to be monitored and controlled to ensure the quality and safety of the medication.

How is Pramipexole Impurity 21 produced during the synthesis of Pramipexole?

It may result from incomplete reactions, side reactions, or degradation of Pramipexole during manufacturing.

What are the implications of the presence of Pramipexole Impurity 21 in pharmaceutical formulations?

It can affect the efficacy, stability, and safety of the drug, leading to potential risks for patients.

How is Pramipexole Impurity 21 detected and quantified in pharmaceutical samples?

Analytical techniques such as chromatography and spectroscopy can be used for identification and quantification.

What measures can be taken to minimize the formation of Pramipexole Impurity 21 during drug manufacturing?

Careful process optimization, monitoring reaction conditions, and ensuring purity of starting materials can help reduce impurity levels.

Are there regulatory guidelines in place regarding the acceptable levels of Pramipexole Impurity 21 in pharmaceutical products?

Yes, regulatory authorities set limits on impurity levels in drugs to ensure safety and quality standards are met.

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