Alfuzosin EP Impurity B

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For Research Use Only | Not For Clinical Use

CAT	APB03230
Synonyms	2-chloro-6,7-dimethoxyquinazolin-4-amine
Molecular Weight	239.66
Molecular Formula	C10H10ClN3O2

What is the molecular weight of Alfuzosin EP Impurity B?

The molecular weight of Alfuzosin EP Impurity B is 239.66.

What is an other name for Alfuzosin EP Impurity B?

An other name for Alfuzosin EP Impurity B is 2-chloro-6,7-dimethoxyquinazolin-4-amine.

What is the molecular formula of Alfuzosin EP Impurity B?

The molecular formula of Alfuzosin EP Impurity B is C10H10ClN3O2.

What is the chemical structure of Alfuzosin EP Impurity B?

The chemical structure of Alfuzosin EP Impurity B is a quinazoline ring with a chlorine atom at position 2 and two methoxy groups at positions 6 and 7.

What is the role of Alfuzosin EP Impurity B in pharmaceuticals?

Alfuzosin EP Impurity B is a known impurity that can be present in the pharmaceutical formulation of Alfuzosin, a medication used to treat symptoms of benign prostatic hyperplasia.

Is Alfuzosin EP Impurity B a common impurity found in Alfuzosin formulations?

Alfuzosin EP Impurity B is not a common impurity found in Alfuzosin formulations, but it is important to monitor and control impurities in pharmaceutical products for safety and efficacy.

How can Alfuzosin EP Impurity B be detected and quantified in pharmaceutical samples?

Alfuzosin EP Impurity B can be detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry.

What are the potential risks associated with the presence of impurities like Alfuzosin EP Impurity B in pharmaceutical products?

The presence of impurities in pharmaceutical products can pose risks to patient safety, including potential adverse effects or decreased efficacy of the medication.

How can pharmaceutical manufacturers ensure the purity of Alfuzosin formulations?

Pharmaceutical manufacturers can ensure the purity of Alfuzosin formulations by conducting thorough quality control testing, monitoring impurities, and following strict regulatory guidelines.

Are there specific guidelines or limits set for the levels of impurities like Alfuzosin EP Impurity B in pharmaceutical products?

Regulatory agencies may set specific guidelines or limits for impurities in pharmaceutical products, including Alfuzosin EP Impurity B, to ensure product safety and quality.

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