Lapatinib Impurity 1

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For Research Use Only | Not For Clinical Use

CAT	APB202197260
CAS	202197-26-0
Structure
Molecular Weight	251.69
Molecular Formula	C13H11ClFNO

What is the product name of CAS 202197-26-0?

The product name is Lapatinib Impurity 1.

What is the molecular weight of Lapatinib Impurity 1?

The molecular weight is 251.69.

What is the molecular formula of Lapatinib Impurity 1?

The molecular formula is C13H11ClFNO.

What is the chemical structure of Lapatinib Impurity 1?

The chemical structure is composed of 13 carbon atoms, 11 hydrogen atoms, 1 chlorine atom, 1 fluorine atom, and 1 nitrogen atom.

How is Lapatinib Impurity 1 different from Lapatinib?

Lapatinib Impurity 1 is a related compound or impurity of Lapatinib, which may be present in small amounts in the final drug product.

What is the significance of identifying and characterizing impurities like Lapatinib Impurity 1?

Identifying and characterizing impurities is crucial in pharmaceutical development to ensure the safety, efficacy, and quality of the final drug product.

How is Lapatinib Impurity 1 typically detected and quantified in pharmaceuticals?

Lapatinib Impurity 1 is often detected and quantified using analytical techniques such as HPLC (High-Performance Liquid Chromatography) or GC (Gas Chromatography).

What are some potential sources of Lapatinib Impurity 1 in the manufacturing process?

Lapatinib Impurity 1 may arise as a byproduct of the synthesis or degradation of Lapatinib during the manufacturing process.

What are the potential risks associated with the presence of impurities like Lapatinib Impurity 1 in pharmaceutical products?

Impurities like Lapatinib Impurity 1 may pose risks to patient safety, trigger adverse reactions, or impact the stability and shelf-life of the drug product.

How can pharmaceutical companies ensure the control and reduction of impurities like Lapatinib Impurity 1 in their products?

Pharmaceutical companies can implement rigorous quality control measures, analytical testing, and process optimizations to minimize the presence of impurities like Lapatinib Impurity 1 in their final drug products.

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