Crizotinib Impurity 42

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For Research Use Only | Not For Clinical Use

CAT	APB877397676
CAS	877397-67-6
Molecular Weight	251.08
Molecular Formula	C10H9Cl2FO2

What is the product name of CAS 877397-67-6?

The product name is Crizotinib Impurity 42.

What is the molecular weight of Crizotinib Impurity 42?

The molecular weight is 251.08.

What is the molecular formula of Crizotinib Impurity 42?

The molecular formula is C10H9Cl2FO2.

What is the chemical structure of Crizotinib Impurity 42?

The chemical structure is composed of 10 carbon atoms, 9 hydrogen atoms, 2 chlorine atoms, 1 fluorine atom, and 2 oxygen atoms.

How is Crizotinib Impurity 42 related to the compound Crizotinib?

Crizotinib Impurity 42 is a related compound or impurity of Crizotinib, which is a drug used in the treatment of certain types of cancer.

What role does Crizotinib Impurity 42 play in the manufacturing process of Crizotinib?

Crizotinib Impurity 42 is a byproduct or impurity that may form during the synthesis or purification process of Crizotinib.

How is Crizotinib Impurity 42 detected and controlled during the production of Crizotinib?

Analytical methods such as HPLC (High Performance Liquid Chromatography) may be used to detect and quantify Crizotinib Impurity 42, and measures are taken to control its presence within acceptable limits.

What are the properties of Crizotinib Impurity 42 that make it distinct from other compounds or impurities?

Its molecular formula and structure containing chlorine, fluorine, and oxygen atoms contribute to its unique properties.

Can Crizotinib Impurity 42 affect the efficacy or safety of Crizotinib?

The presence of impurities, including Crizotinib Impurity 42, can potentially impact the purity, safety, or efficacy of the final drug product and must be carefully monitored and controlled.

Are there regulatory guidelines or limits established for Crizotinib Impurity 42 in the production of Crizotinib?

Yes, regulatory authorities such as the FDA may set specific limits or acceptance criteria for impurities, including Crizotinib Impurity 42, to ensure the quality and safety of pharmaceutical products.

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