Brivaracetam Impurity 54

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For Research Use Only | Not For Clinical Use

CAT	APB01239
Synonyms	(2S)-methyl 2-((5-oxo-3-propyl-2,5-dihydrofuran-2-yl)amino)butanoate
Molecular Weight	241.28
Molecular Formula	C12H19NO4

What is the chemical name of Brivaracetam Impurity 54?

The chemical name of Brivaracetam Impurity 54 is (2S)-methyl 2-((5-oxo-3-propyl-2,5-dihydrofuran-2-yl)amino)butanoate.

What is the molecular weight of Brivaracetam Impurity 54?

The molecular weight of Brivaracetam Impurity 54 is 241.28.

What is the molecular formula of Brivaracetam Impurity 54?

The molecular formula of Brivaracetam Impurity 54 is C12H19NO4.

How is Brivaracetam Impurity 54 synthesized?

Brivaracetam Impurity 54 is synthesized from the (2S)-methyl ester and propyl-substituted amorolfine.

What are some synonyms for Brivaracetam Impurity 54?

Some synonyms for Brivaracetam Impurity 54 include (2S)-methyl 2-((5-oxo-3-propyl-2,5-dihydrofuran-2-yl)amino)butanoate.

Why is it important to identify and characterize impurities like Brivaracetam Impurity 54?

Identifying and characterizing impurities like Brivaracetam Impurity 54 is important for ensuring the safety and efficacy of the final pharmaceutical product.

How can Brivaracetam Impurity 54 affect the stability of a drug product?

Brivaracetam Impurity 54 can impact the stability of a drug product by potentially reacting with other components and forming new impurities.

Are there specific regulations regarding the levels of Brivaracetam Impurity 54 allowed in pharmaceutical products?

Yes, regulatory agencies typically have guidelines for the maximum acceptable levels of impurities like Brivaracetam Impurity 54 in pharmaceutical products.

What methods can be used to detect and quantify Brivaracetam Impurity 54?

Techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry can be used to detect and quantify Brivaracetam Impurity 54.

How can the presence of Brivaracetam Impurity 54 impact the effectiveness of a drug product?

The presence of Brivaracetam Impurity 54 can impact the effectiveness of a drug product by potentially interfering with the intended pharmacological activity or causing adverse effects.

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