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Ciclopirox Olamine EP Impurity A

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For Research Use Only | Not For Clinical Use
CATAPB1823487531
CAS1823487-53-1
Molecular Weight225.29
Molecular FormulaC12H19NO3

What is the name of the product?

Ciclopirox Olamine EP Impurity A

What is the chemical formula of Ciclopirox Olamine EP Impurity A?

C12H19NO3

What is the molecular weight of Ciclopirox Olamine EP Impurity A?

225.29

What is the CAS number of Ciclopirox Olamine EP Impurity A?

1823487-53-1

What is the significance of identifying impurities in pharmaceutical products?

Identifying impurities ensures the safety and efficacy of the drug product.

How is Ciclopirox Olamine EP Impurity A categorized in terms of its chemical class?

It is classified as an EP impurity.

How does the presence of impurities in drug substances affect their quality?

Impurities can affect the stability, safety, and effectiveness of drug substances.

What methods are typically used to detect and quantify impurities in pharmaceutical products?

Methods such as HPLC (High Performance Liquid Chromatography) are commonly used for impurity analysis.

Why is it important for pharmaceutical manufacturers to control impurities in their products?

Controlling impurities ensures that the drug product meets regulatory standards for safety and quality.

In what ways can impurity profiling help in the development of new drug formulations?

Impurity profiling can help in understanding the degradation pathways of drug substances and optimizing the manufacturing process to reduce impurity levels.

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