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Azelastine Impurity 10

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For Research Use Only | Not For Clinical Use
CATAPB6315602
CAS6315-60-2
Structure
Molecular Weight231.29
Molecular FormulaC11H21NO4

What is the product name of Azelastine Impurity 10?

The product name of Azelastine Impurity 10 is Azelastine Impurity 10.

What is the CAS number of Azelastine Impurity 10?

The CAS number of Azelastine Impurity 10 is 6315-60-2.

What is the molecular weight of Azelastine Impurity 10?

The molecular weight of Azelastine Impurity 10 is 231.29.

What is the molecular formula of Azelastine Impurity 10?

The molecular formula of Azelastine Impurity 10 is C11H21NO4.

What are the chemical elements present in the molecular formula of Azelastine Impurity 10?

Carbon (C), Hydrogen (H), Nitrogen (N), and Oxygen (O) are the chemical elements present in the molecular formula of Azelastine Impurity 10.

What is the significance of identifying impurities in pharmaceutical products?

Identifying impurities in pharmaceutical products is important for ensuring the safety, efficacy, and quality of the product.

How is Azelastine Impurity 10 typically characterized and analyzed in a laboratory setting?

Azelastine Impurity 10 is typically characterized and analyzed using analytical techniques such as HPLC (High-Performance Liquid Chromatography) and spectroscopy.

Why is it important to control impurities in pharmaceutical products during the manufacturing process?

Controlling impurities in pharmaceutical products during the manufacturing process is essential to meet regulatory standards, ensure product stability, and prevent potential adverse effects on patients.

Can impurities in pharmaceutical products affect the bioavailability of the active ingredient?

Yes, impurities in pharmaceutical products can affect the bioavailability of the active ingredient, potentially impacting the therapeutic efficacy of the medication.

How can manufacturers prevent the formation of impurities in pharmaceutical products like Azelastine Impurity 10?

Manufacturers can prevent the formation of impurities in pharmaceutical products by implementing strict quality control measures, using high-quality raw materials, and maintaining proper manufacturing conditions.

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