Lisinopril EP Impurity A

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For Research Use Only | Not For Clinical Use

What is the name of the product for CAS 1012-05-1?

The product name is Lisinopril EP Impurity A.

What is the molecular weight of Lisinopril EP Impurity A?

The molecular weight is 179.21.

What is the molecular formula of Lisinopril EP Impurity A?

The molecular formula is C10H13NO2.

How is Lisinopril EP Impurity A characterized?

Lisinopril EP Impurity A is characterized by its CAS number 1012-05-1.

What are the elements present in the molecular formula of Lisinopril EP Impurity A?

The molecular formula contains carbon, hydrogen, nitrogen, and oxygen.

Why is it important to identify impurities such as Lisinopril EP Impurity A in pharmaceutical products?

Identifying impurities like Lisinopril EP Impurity A is important for quality control and ensuring the safety of pharmaceutical products.

Are there specific tests or methods used to detect Lisinopril EP Impurity A?

Yes, there may be specific tests or methods used to detect and quantify Lisinopril EP Impurity A in pharmaceutical products.

What potential effects could the presence of Lisinopril EP Impurity A have on the efficacy of a drug product?

The presence of impurities like Lisinopril EP Impurity A could affect the efficacy, safety, and stability of a drug product.

How can manufacturers ensure that the levels of Lisinopril EP Impurity A in their products are within acceptable limits?

Manufacturers can use analytical techniques and strict quality control measures to monitor and control impurity levels in their products.

Is Lisinopril EP Impurity A a controlled substance or strictly regulated compound?

The regulation of Lisinopril EP Impurity A may vary depending on the country or region, but it is not typically considered a controlled substance.

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