Saxagliptin Impurity 54

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For Research Use Only | Not For Clinical Use

CAT	APB1417743419
CAS	1417743-41-9
Molecular Weight	227.26
Molecular Formula	C11H17NO4

What is the product name of CAS 1417743-41-9?

The product name is Saxagliptin Impurity 54.

What is the molecular weight of Saxagliptin Impurity 54?

The molecular weight is 227.26.

What is the molecular formula of Saxagliptin Impurity 54?

The molecular formula is C11H17NO4.

What is the chemical structure of Saxagliptin Impurity 54?

The chemical structure is composed of 11 carbon atoms, 17 hydrogen atoms, one nitrogen atom, and four oxygen atoms arranged in a specific configuration.

What is the significance of identifying impurities in pharmaceutical products?

Identifying impurities in pharmaceutical products is important for ensuring the safety, efficacy, and quality of the final drug product.

How can Saxagliptin Impurity 54 impact the effectiveness of the drug Saxagliptin?

If present in significant amounts, Saxagliptin Impurity 54 may affect the potency or stability of Saxagliptin, potentially reducing its therapeutic effectiveness.

What are some methods used to detect and characterize impurities in pharmaceutical products?

Techniques such as high-performance liquid chromatography (HPLC), mass spectrometry, and nuclear magnetic resonance (NMR) spectroscopy are commonly used to detect and characterize impurities.

How can the presence of impurities in pharmaceutical products be controlled or minimized?

Strict quality control measures, good manufacturing practices, and thorough analytical testing can help control or minimize the presence of impurities in pharmaceutical products.

Are impurities always harmful in pharmaceutical products?

Not necessarily. Some impurities may be harmless or present in trace amounts that do not affect the safety or efficacy of the drug product.

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

Monitoring and controlling impurities in pharmaceutical products is crucial for maintaining regulatory compliance, ensuring patient safety, and producing high-quality medications.

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