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Levofloxacin EP Impurity F

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For Research Use Only | Not For Clinical Use
CATAPB100986898
CAS100986-89-8
Structure
Molecular Weight281.22
Molecular FormulaC13H9F2NO4

What is the molecular weight of Levofloxacin EP Impurity F?

The molecular weight of Levofloxacin EP Impurity F is 281.22.

What is the molecular formula of Levofloxacin EP Impurity F?

The molecular formula of Levofloxacin EP Impurity F is C13H9F2NO4.

What is the CAS number of Levofloxacin EP Impurity F?

The CAS number of Levofloxacin EP Impurity F is 100986-89-8.

What is the significance of Levofloxacin EP Impurity F in pharmaceutical research?

Levofloxacin EP Impurity F is an impurity that may affect the quality and purity of Levofloxacin in pharmaceutical formulations.

How is Levofloxacin EP Impurity F synthesized?

Levofloxacin EP Impurity F is likely synthesized as a byproduct or impurity during the production of Levofloxacin.

Can Levofloxacin EP Impurity F impact the efficacy of Levofloxacin in treating infections?

The presence of Levofloxacin EP Impurity F in a formulation may impact the efficacy of Levofloxacin, as it may alter the drug's pharmacological properties.

How is Levofloxacin EP Impurity F detected in pharmaceutical formulations?

Levofloxacin EP Impurity F can be detected using analytical techniques such as HPLC or LC-MS.

What precautions should be taken to minimize the presence of Levofloxacin EP Impurity F in pharmaceutical products?

Manufacturers should ensure proper purification and quality control processes to minimize the presence of Levofloxacin EP Impurity F in pharmaceutical products.

Are there regulatory limits for the presence of Levofloxacin EP Impurity F in pharmaceutical products?

Regulatory bodies may have established limits for impurity levels in pharmaceutical products, including Levofloxacin EP Impurity F, to ensure product quality and safety.

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