Lenvatinib Impurity 52

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For Research Use Only | Not For Clinical Use

CAT	APB08380
Molecular Weight	265.7
Molecular Formula	C12H12ClN3O2

What is the molecular weight of Lenvatinib Impurity 52?

The molecular weight of Lenvatinib Impurity 52 is 265.7.

What is the molecular formula of Lenvatinib Impurity 52?

The molecular formula of Lenvatinib Impurity 52 is C12H12ClN3O2.

What is the chemical structure of Lenvatinib Impurity 52 based on its molecular formula?

The chemical structure of Lenvatinib Impurity 52 based on its molecular formula C12H12ClN3O2 would consist of a carbon backbone with hydrogen, chlorine, nitrogen, and oxygen atoms arranged accordingly.

How is Lenvatinib Impurity 52 related to the drug Lenvatinib?

Lenvatinib Impurity 52 is likely a related compound or impurity associated with the drug Lenvatinib, which is used in cancer treatment.

Is Lenvatinib Impurity 52 a known impurity in the production of Lenvatinib?

Yes, Lenvatinib Impurity 52 is listed as an impurity in the production of Lenvatinib.

What is the significance of knowing the molecular weight of Lenvatinib Impurity 52?

Understanding the molecular weight of Lenvatinib Impurity 52 can help in analyzing its properties and behavior in chemical reactions.

How are impurities like Lenvatinib Impurity 52 typically removed during drug manufacturing?

Impurities like Lenvatinib Impurity 52 are typically removed through purification processes such as filtration, distillation, or chromatography.

Are impurities such as Lenvatinib Impurity 52 harmful to consumers if present in the drug product?

Impurities like Lenvatinib Impurity 52 can be harmful if present in significant amounts in the drug product, which is why regulatory agencies set strict limits on impurity levels.

Can Lenvatinib Impurity 52 affect the efficacy of the drug Lenvatinib?

If Lenvatinib Impurity 52 is present in high concentrations, it could potentially impact the efficacy of the drug Lenvatinib.

How is Lenvatinib Impurity 52 identified and characterized during the drug development process?

Lenvatinib Impurity 52 is identified and characterized through analytical techniques such as chromatography, spectroscopy, and mass spectrometry during the drug development process.

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