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Perindopril EP Impurity L

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For Research Use Only | Not For Clinical Use
CATAPB111836227
CAS111836-22-7
Molecular Weight211.26
Molecular FormulaC11H17NO3

What is the name of the product?

The impurity is named Perindopril EP Impurity L.

What is the CAS number assigned to Perindopril EP Impurity L?

The CAS number assigned to Perindopril EP Impurity L is 111836-22-7.

What is the molecular weight of Perindopril EP Impurity L?

The molecular weight of Perindopril EP Impurity L is 211.26.

What is the molecular formula of Perindopril EP Impurity L?

The molecular formula of Perindopril EP Impurity L is C11H17NO3.

How does Perindopril EP Impurity L compare to the main drug component in terms of molecular weight?

Perindopril EP Impurity L has a molecular weight of 211.26, compared to the main drug component Perindopril which has a molecular weight of approximately 368.49.

Why is it important to identify and characterize impurities such as Perindopril EP Impurity L in pharmaceutical products?

It is important to identify and characterize impurities in pharmaceutical products due to concerns about safety, efficacy, and regulatory compliance.

How can the presence of Perindopril EP Impurity L affect the quality of the final drug product?

The presence of impurities such as Perindopril EP Impurity L can affect the potency, stability, and overall quality of the final drug product.

What methods are used to detect and quantify impurities like Perindopril EP Impurity L in pharmaceutical formulations?

Analytical techniques such as high-performance liquid chromatography (HPLC) and mass spectrometry are commonly used to detect and quantify impurities in pharmaceutical formulations.

Are there regulatory limits for impurities like Perindopril EP Impurity L in pharmaceutical products?

Yes, regulatory authorities set limits on the levels of impurities that are allowed in pharmaceutical products to ensure safety and quality.

What steps can be taken to minimize the presence of impurities like Perindopril EP Impurity L during the manufacturing process?

Manufacturers can implement good manufacturing practices (GMP), stringent quality control measures, and proper purification techniques to minimize the presence of impurities in pharmaceutical products.

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