Entecavir USP Impurity A

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For Research Use Only | Not For Clinical Use

CAT	APB1984788966
CAS	1984788-96-6
Molecular Weight	293.28
Molecular Formula	C12H15N5O4

What is the name of the impurity identified as CAS 1984788-96-6 in Entecavir?

The impurity is identified as Entecavir USP Impurity A.

What is the molecular weight of Entecavir USP Impurity A?

The molecular weight of Entecavir USP Impurity A is 293.28.

What is the molecular formula of Entecavir USP Impurity A?

The molecular formula of Entecavir USP Impurity A is C12H15N5O4.

Is Entecavir USP Impurity A a chemical compound or impurity?

Entecavir USP Impurity A is an impurity.

In what industry is Entecavir USP Impurity A commonly found?

Entecavir USP Impurity A is commonly found in the pharmaceutical industry.

Is Entecavir USP Impurity A used as an active ingredient in medications?

No, Entecavir USP Impurity A is not used as an active ingredient in medications.

Can Entecavir USP Impurity A impact the effectiveness or safety of medications?

Yes, impurities like Entecavir USP Impurity A can impact the effectiveness or safety of medications.

How is Entecavir USP Impurity A identified and characterized in pharmaceutical products?

Entecavir USP Impurity A is identified and characterized through analytical techniques such as chromatography and spectroscopy.

Why is it important to monitor and control impurities like Entecavir USP Impurity A in pharmaceutical products?

It is important to monitor and control impurities in pharmaceutical products to ensure the safety, efficacy, and quality of the medications produced.

Are regulations in place to lim- It the presence of impurities like Entecavir USP Impurity A in pharmaceutical products?

Yes, regulatory authorities have guidelines and limits in place to restrict the presence of impurities like Entecavir USP Impurity A in pharmaceutical products.

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