Lenvatinib Impurity 19

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For Research Use Only | Not For Clinical Use

CAT	APB417724813
CAS	417724-81-3
Molecular Weight	218.21
Molecular Formula	C11H10N2O3

What is the product name of CAS 417724-81-3?

The product name of CAS 417724-81-3 is Lenvatinib Impurity 19.

What is the molecular weight of Lenvatinib Impurity 19?

The molecular weight of Lenvatinib Impurity 19 is 218.21.

What is the molecular formula of Lenvatinib Impurity 19?

The molecular formula of Lenvatinib Impurity 19 is C11H10N2O3.

What is the chemical structure of Lenvatinib Impurity 19 based on its molecular formula?

The chemical structure of Lenvatinib Impurity 19 based on its molecular formula C11H10N2O3 would include 11 carbon atoms, 10 hydrogen atoms, 2 nitrogen atoms, and 3 oxygen atoms.

How does Lenvatinib Impurity 19 relate to the drug Lenvatinib?

Lenvatinib Impurity 19 is likely a byproduct or impurity in the synthesis or manufacturing process of the drug Lenvatinib.

What potential effects can Lenvatinib Impurity 19 have if present in the final drug product?

Lenvatinib Impurity 19 could potentially affect the purity, efficacy, and safety of the final drug product if present in significant quantities.

Is Lenvatinib Impurity 19 a known toxic substance?

Without specific toxicity data, it cannot be definitively stated Whether Lenvatinib Impurity 19 is a toxic substance or not.

How is Lenvatinib Impurity 19 typically identified and characterized in pharmaceutical manufacturing?

Lenvatinib Impurity 19 is typically identified and characterized using analytical techniques such as chromatography, spectroscopy, and mass spectrometry.

Are there regulatory guidelines or limits regarding the presence of Lenvatinib Impurity 19 in pharmaceutical products?

Regulatory bodies such as the FDA may have established guidelines or limits on the acceptable levels of Lenvatinib Impurity 19 in pharmaceutical products.

What steps can pharmaceutical manufacturers take to minimize the presence of impurities like Lenvatinib Impurity 19 in their products?

Pharmaceutical manufacturers can implement stringent quality control measures, optimize synthetic routes, and conduct thorough impurity testing to minimize the presence of impurities like Lenvatinib Impurity 19 in their products.

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