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Lenvatinib Impurity 17

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For Research Use Only | Not For Clinical Use
CATAPB08370
Molecular Weight250.68
Molecular FormulaC12H11ClN2O2

What is the molecular weight of Lenvatinib Impurity 17?

The molecular weight of Lenvatinib Impurity 17 is 250.68.

What is the molecular formula of Lenvatinib Impurity 17?

The molecular formula of Lenvatinib Impurity 17 is C12H11ClN2O2.

What is the chemical structure of Lenvatinib Impurity 17 based on its molecular formula?

The chemical structure of Lenvatinib Impurity 17 based on its molecular formula is C12H11ClN2O2.

How does Lenvatinib Impurity 17 relate to the compound Lenvatinib?

Lenvatinib Impurity 17 is a specific impurity associated with the compound Lenvatinib.

What are the potential implications of the presence of Lenvatinib Impurity 17 in a sample of Lenvatinib?

The presence of Lenvatinib Impurity 17 in a sample of Lenvatinib may impact the purity and efficacy of the compound.

How is Lenvatinib Impurity 17 typically identified and characterized in a sample?

Lenvatinib Impurity 17 is typically identified and characterized through analytical techniques such as chromatography and spectroscopy.

Are there specific regulatory guidelines regarding the allowable presence of Lenvatinib Impurity 17 in pharmaceutical products?

Yes, there are regulatory guidelines specifying the maximum allowable levels of Lenvatinib Impurity 17 in pharmaceutical products.

Can Lenvatinib Impurity 17 affect the stability of Lenvatinib formulations?

Lenvatinib Impurity 17 can potentially affect the stability and shelf-life of Lenvatinib formulations.

What steps can be taken to minimize the presence of Lenvatinib Impurity 17 in Lenvatinib products?

Purification processes and quality control measures can be implemented to minimize the presence of Lenvatinib Impurity 17 in Lenvatinib products.

Are there specific methods available for the quantification of Lenvatinib Impurity 17 levels in pharmaceutical samples?

Yes, there are validated methods for quantifying the levels of Lenvatinib Impurity 17 in pharmaceutical samples, ensuring compliance with regulatory standards.

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