Pramipexole Impurity 28

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For Research Use Only | Not For Clinical Use

CAT	APB936751110
CAS	936751-11-0
Structure
Molecular Weight	243.33
Molecular Formula	C10H17N3O2S

What is the product name of CAS 936751-11-0?

The product name is Pramipexole Impurity 28.

What is the molecular weight of Pramipexole Impurity 28?

The molecular weight of Pramipexole Impurity 28 is 243.33.

What is the molecular formula of Pramipexole Impurity 28?

The molecular formula of Pramipexole Impurity 28 is C10H17N3O2S.

What is the chemical structure of Pramipexole Impurity 28 based on its molecular formula?

The chemical structure of Pramipexole Impurity 28 includes 10 carbon atoms, 17 hydrogen atoms, 3 nitrogen atoms, 2 oxygen atoms, and 1 sulfur atom.

What is the significance of Pramipexole Impurity 28 in pharmaceutical research?

Pramipexole Impurity 28 is a specific impurity related to the drug pramipexole, which is used to treat Parkinson's disease and restless legs syndrome. Its identification and characterization are crucial for quality control in pharmaceutical manufacturing.

How is Pramipexole Impurity 28 synthesized in the laboratory?

The synthesis of Pramipexole Impurity 28 may involve organic chemical reactions starting from precursor molecules that ultimately lead to the formation of the impurity.

What analytical techniques can be used to identify and quantify Pramipexole Impurity 28?

Analytical techniques such as high-performance liquid chromatography (HPLC), mass spectrometry, and nuclear magnetic resonance (NMR) spectroscopy can be employed for the analysis of Pramipexole Impurity 28.

How does the presence of Pramipexole Impurity 28 affect the quality of pharmaceutical products containing pramipexole?

The presence of impurities like Pramipexole Impurity 28 can affect the efficacy and safety of pharmaceutical products, leading to potential regulatory concerns and patient safety issues.

Are there regulatory limits or guidelines for the maximum allowable levels of Pramipexole Impurity 28 in pharmaceutical formulations?

Regulatory bodies such as the FDA may establish limits or guidelines for impurity levels, including Pramipexole Impurity 28, in pharmaceutical products to ensure safety and quality standards are met.

What measures can be taken to minimize the formation of Pramipexole Impurity 28 during the manufacturing and storage of pramipexole-containing drugs?

Strict quality control measures, proper storage conditions, and monitoring of manufacturing processes can help minimize the formation of impurities like Pramipexole Impurity 28 in pharmaceutical products.

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