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Levofloxacin Impurity P

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For Research Use Only | Not For Clinical Use
CATAPB157766273
CAS157766-27-3
Molecular Weight246.18
Molecular FormulaC11H9F3O3

What is the CAS number for Levofloxacin Impurity P?

The CAS number for Levofloxacin Impurity P is 157766-27-3.

What is the molecular weight of Levofloxacin Impurity P?

The molecular weight of Levofloxacin Impurity P is 246.18.

What is the molecular formula of Levofloxacin Impurity P?

The molecular formula of Levofloxacin Impurity P is C11H9F3O3.

What is the chemical structure of Levofloxacin Impurity P?

The chemical structure of Levofloxacin Impurity P is composed of 11 carbon atoms, 9 hydrogen atoms, 3 fluorine atoms, and 3 oxygen atoms.

What is the significance of Levofloxacin Impurity P in pharmaceutical research?

Levofloxacin Impurity P is important in pharmaceutical research as it is an impurity that needs to be monitored and controlled in the production of the drug Levofloxacin.

How is Levofloxacin Impurity P detected and quantified in pharmaceutical formulations?

Levofloxacin Impurity P can be detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) and mass spectrometry.

Why is it important to control impurities like Levofloxacin Impurity P in pharmaceutical products?

Controlling impurities like Levofloxacin Impurity P is important to ensure the safety, efficacy, and quality of pharmaceutical products.

What are the potential sources of Levofloxacin Impurity P in pharmaceutical manufacturing?

Levofloxacin Impurity P can be introduced during the synthesis of Levofloxacin or as a degradation product of the active pharmaceutical ingredient.

How does the presence of Levofloxacin Impurity P affect the stability of pharmaceutical products?

The presence of Levofloxacin Impurity P can affect the stability of pharmaceutical products by potentially reducing the shelf life or efficacy of the drug.

How can pharmaceutical manufacturers reduce the levels of Levofloxacin Impurity P in their products?

Pharmaceutical manufacturers can reduce the levels of Levofloxacin Impurity P in their products through process optimization, strict quality control measures, and proper handling of raw materials.

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