Nebivolol Impurity 71

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For Research Use Only | Not For Clinical Use

CAT	APB01445
Synonyms	(2R)-6-fluoro-2-(oxiran-2-yl)chroman
Molecular Weight	194.20
Molecular Formula	C11H11FO2

What is the chemical name of Nebivolol Impurity 71?

The chemical name of Nebivolol Impurity 71 is (2R)-6-fluoro-2-(oxiran-2-yl)chroman.

What is the molecular weight of Nebivolol Impurity 71?

The molecular weight of Nebivolol Impurity 71 is 194.20.

What is the molecular formula of Nebivolol Impurity 71?

The molecular formula of Nebivolol Impurity 71 is C11H11FO2.

What is the structure of Nebivolol Impurity 71 based on its molecular formula?

The structure of Nebivolol Impurity 71 is a chroman ring with a fluoro and oxiran group attached.

Why is Nebivolol Impurity 71 considered an impurity?

Nebivolol Impurity 71 is considered an impurity because it is a byproduct or contaminant in the synthesis of nebivolol.

What is the significance of the presence of Nebivolol Impurity 71 in nebivolol production?

The presence of Nebivolol Impurity 71 in nebivolol production can affect the quality and purity of the final product.

How is Nebivolol Impurity 71 typically removed from nebivolol during manufacturing?

Nebivolol Impurity 71 is typically removed from nebivolol during manufacturing through purification techniques such as chromatography.

Are there specific regulatory limits for Nebivolol Impurity 71 in pharmaceutical products?

Yes, regulatory authorities may set specific limits on the presence of Nebivolol Impurity 71 in pharmaceutical products to ensure safety and efficacy.

What are the potential risks associated with the presence of Nebivolol Impurity 71 in nebivolol formulations?

The potential risks associated with the presence of Nebivolol Impurity 71 in nebivolol formulations include reduced effectiveness, potential toxicity, and adverse reactions in patients.

What measures can be taken to minimize the formation of Nebivolol Impurity 71 during the synthesis of nebivolol?

Measures such as optimizing reaction conditions, purification processes, and quality control procedures can be implemented to minimize the formation of Nebivolol Impurity 71 during the synthesis of nebivolol.

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