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Pramipexole EP Impurity E

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For Research Use Only | Not For Clinical Use
CATAPB106006842
CAS106006-84-2
Structure
Molecular Weight225.31
Molecular FormulaC10H15N3OS

What is the full name of the compound with CAS number 106006-84-2?

The full name of the compound is Pramipexole EP Impurity E.

What is the molecular weight of Pramipexole EP Impurity E?

The molecular weight of Pramipexole EP Impurity E is 225.31.

What is the molecular formula of Pramipexole EP Impurity E?

The molecular formula of Pramipexole EP Impurity E is C10H15N3OS.

What is the structure of Pramipexole EP Impurity E based on its molecular formula?

The structure of Pramipexole EP Impurity E based on its molecular formula, C10H15N3OS, includes elements carbon, hydrogen, nitrogen, and sulfur.

What is the significance of Pramipexole EP Impurity E in pharmaceuticals?

Pramipexole EP Impurity E is important in pharmaceuticals as an impurity of the drug Pramipexole.

How is Pramipexole EP Impurity E detected in pharmaceutical products?

Pramipexole EP Impurity E can be detected using analytical techniques such as chromatography and spectroscopy.

What is the role of CAS number 106006-84-2 in identifying Pramipexole EP Impurity E?

CAS number 106006-84-2 is a unique numerical identifier assigned to Pramipexole EP Impurity E, helping in its identification and classification.

How can Pramipexole EP Impurity E impact the quality of pharmaceutical products?

Pramipexole EP Impurity E can impact the quality of pharmaceutical products by affecting their purity and efficacy.

Are there regulations regarding the permissible levels of Pramipexole EP Impurity E in pharmaceutical formulations?

Yes, regulatory agencies like the FDA may have guidelines or limits on the acceptable levels of Pramipexole EP Impurity E in pharmaceutical formulations.

What precautions should be taken during the manufacturing process to minimize the presence of Pramipexole EP Impurity E?

Manufacturers should implement strict quality control measures, conduct thorough testing, and adhere to Good Manufacturing Practices to minimize the presence of Pramipexole EP Impurity E in pharmaceutical products.

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