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Lenalidomide Impurity 12

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For Research Use Only | Not For Clinical Use
CATAPB295357721
CAS295357-72-1
Molecular Weight308.25
Molecular FormulaC13H12N2O7

What is the specific name of the product?

The specific name of the product is Lenalidomide Impurity 12.

What is the CAS number of Lenalidomide Impurity 12?

The CAS number of Lenalidomide Impurity 12 is 295357-72-1.

What is the molecular weight of Lenalidomide Impurity 12?

The molecular weight of Lenalidomide Impurity 12 is 308.25.

What is the molecular formula of Lenalidomide Impurity 12?

The molecular formula of Lenalidomide Impurity 12 is C13H12N2O7.

What is the structure of Lenalidomide Impurity 12 based on its molecular formula?

Based on its molecular formula, the structure of Lenalidomide Impurity 12 consists of 13 Carbon atoms, 12 Hydrogen atoms, 2 Nitrogen atoms, and 7 Oxygen atoms.

What is the significance of identifying impurities in lenalidomide products?

Identifying impurities in lenalidomide products is crucial because impurities can affect the safety and efficacy of the medication and need to be monitored and controlled.

How is Lenalidomide Impurity 12 typically detected and quantified in pharmaceutical samples?

Lenalidomide Impurity 12 is typically detected and quantified through various analytical techniques such as HPLC (High-Performance Liquid Chromatography) and mass spectrometry.

What are the potential sources of Lenalidomide Impurity 12 in pharmaceutical manufacturing processes?

Potential sources of Lenalidomide Impurity 12 in pharmaceutical manufacturing processes include synthesis by-products, degradation products, and impurities from raw materials.

How do regulatory bodies like the FDA (Food and Drug Administration) address the presence of impurities in pharmaceutical products like lenalidomide?

Regulatory bodies like the FDA set limits on impurities in pharmaceutical products like lenalidomide and require manufacturers to monitor and control impurities to ensure product quality and safety.

How can the presence of Lenalidomide Impurity 12 affect the stability and shelf-life of lenalidomide products?

The presence of Lenalidomide Impurity 12 can affect the stability and shelf-life of lenalidomide products by potentially compromising the drug's efficacy, safety, and overall quality.

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