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Levofloxacin Impurity 32

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For Research Use Only | Not For Clinical Use
CATAPB1026952919
CAS1026952-91-9
Molecular Weight283.23
Molecular FormulaC13H11F2NO4

What is the CAS number for Levofloxacin Impurity 32?

The CAS number for Levofloxacin Impurity 32 is 1026952-91-9.

What is the molecular weight of Levofloxacin Impurity 32?

The molecular weight of Levofloxacin Impurity 32 is 283.23.

What is the molecular formula of Levofloxacin Impurity 32?

The molecular formula of Levofloxacin Impurity 32 is C13H11F2NO4.

What structural properties does Levofloxacin Impurity 32 have based on its molecular formula?

Levofloxacin Impurity 32 contains 13 carbon atoms, 11 hydrogen atoms, 2 fluorine atoms, 1 nitrogen atom, and 4 oxygen atoms in its structure.

How does Levofloxacin Impurity 32 differ from the main drug Levofloxacin?

Levofloxacin Impurity 32 is a related compound or impurity of Levofloxacin, which means it may be present as a contaminant in the main drug or during its synthesis.

What are the potential effects of Levofloxacin Impurity 32 in pharmaceutical products?

Levofloxacin Impurity 32 may affect the purity and stability of pharmaceutical products containing Levofloxacin, leading to potential quality issues.

How can Levofloxacin Impurity 32 be detected and quantified in pharmaceutical samples?

Levofloxacin Impurity 32 can be detected and quantified using analytical techniques such as HPLC (High-Performance Liquid Chromatography) or LC-MS (Liquid Chromatography-Mass Spectrometry).

What are the possible sources of Levofloxacin Impurity 32 in pharmaceutical manufacturing?

Levofloxacin Impurity 32 may originate from intermediate reactions, starting materials, or impurities present in raw materials during the manufacturing process of Levofloxacin.

How important is controlling the levels of impurities like Levofloxacin Impurity 32 in pharmaceutical formulations?

Controlling the levels of impurities like Levofloxacin Impurity 32 is crucial for ensuring the safety, efficacy, and quality of pharmaceutical products, as excessive impurities may pose risks to patients.

What steps can be taken to minimize the presence of impurities like Levofloxacin Impurity 32 in pharmaceutical products?

Pharmaceutical manufacturers can implement strict quality control measures, optimize synthesis processes, and use high-quality raw materials to minimize the presence of impurities like Levofloxacin Impurity 32 in their products.

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