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Pramipexole Impurity P

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For Research Use Only | Not For Clinical Use
CATAPB1346617477
CAS1346617-47-7
Structure
Molecular Weight281.38
Molecular FormulaC13H19N3O2S

What is the product name of the compound with CAS number 1346617-47-7?

The product name of the compound is Pramipexole Impurity P.

What is the molecular weight of Pramipexole Impurity P?

The molecular weight of Pramipexole Impurity P is 281.38.

What is the molecular formula of Pramipexole Impurity P?

The molecular formula of Pramipexole Impurity P is C13H19N3O2S.

What is the chemical structure of Pramipexole Impurity P?

The chemical structure consists of 13 Carbon atoms, 19 Hydrogen atoms, 3 Nitrogen atoms, 2 Oxygen atoms, and 1 Sulfur atom.

What is the significance of identifying impurities in pramipexole?

Identifying impurities in pramipexole is important for quality control and regulatory purposes in pharmaceutical manufacturing.

How can Pramipexole Impurity P be synthesized?

Pramipexole Impurity P can be synthesized through organic synthesis processes.

Why is it important to analyze and characterize impurities in pharmaceutical compounds?

It is important to analyze and characterize impurities in pharmaceutical compounds to ensure safety, efficacy, and quality of the final product.

Are impurities always harmful in pharmaceuticals?

Impurities in pharmaceuticals may not always be harmful, but they can affect the potency, stability, and safety of the drug.

How can Pramipexole Impurity P be detected in a pharmaceutical sample?

Pramipexole Impurity P can be detected in a pharmaceutical sample using analytical techniques such as HPLC, LC-MS, or NMR spectroscopy.

What are the potential risks of not controlling impurities in pharmaceutical products?

Not controlling impurities in pharmaceutical products can lead to decreased efficacy, potential toxicity, regulatory issues, and compromised patient safety.

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