Brivaracetam Impurity 36

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For Research Use Only | Not For Clinical Use

CAT	APB2252417175
CAS	2252417-17-5
Synonyms	(R)-N-((S)-1-amino-1-oxobutan-2-yl)-3-(hydroxymethyl)hexanamide
Molecular Weight	230.3
Molecular Formula	C11H22N2O3

What is the product name of CAS 2252417-17-5?

The product name is Brivaracetam Impurity 36.

What is the synonym for Brivaracetam Impurity 36?

The synonym is (R)-N-((S)-1-amino-1-oxobutan-2-yl)-3-(hydroxymethyl)hexanamide.

What is the molecular weight of Brivaracetam Impurity 36?

The molecular weight of Brivaracetam Impurity 36 is 230.3.

What is the molecular formula of Brivaracetam Impurity 36?

The molecular formula of Brivaracetam Impurity 36 is C11H22N2O3.

Can you provide any information on the structure of Brivaracetam Impurity 36 based on its molecular formula?

Based on its molecular formula, the structure of Brivaracetam Impurity 36 contains 11 carbon atoms, 22 hydrogen atoms, 2 nitrogen atoms, and 3 oxygen atoms.

How is Brivaracetam Impurity 36 synthesized?

Brivaracetam Impurity 36 is likely synthesized by chemical reactions that involve the specific combination of (R)-N-((S)-1-amino-1-oxobutan-2-yl)-3-(hydroxymethyl)hexanamide.

What is the significance of Brivaracetam Impurity 36 in pharmaceuticals?

Brivaracetam Impurity 36 is important in pharmaceuticals as it can act as an impurity in the synthesis of Brivaracetam, impacting the purity and effectiveness of the final drug product.

How is Brivaracetam Impurity 36 typically detected and monitored in pharmaceutical manufacturing?

Brivaracetam Impurity 36 is typically detected and monitored through analytical methods such as HPLC (High-Performance Liquid Chromatography) and spectroscopic techniques to ensure the purity of the final drug product.

What are the potential implications of the presence of Brivaracetam Impurity 36 in pharmaceutical products?

The presence of Brivaracetam Impurity 36 in pharmaceutical products can lead to decreased efficacy, safety concerns, and regulatory issues, highlighting the importance of stringent quality control measures in pharmaceutical manufacturing.

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