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Lenvatinib Impurity 18

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For Research Use Only | Not For Clinical Use
CATAPB08371
Molecular Weight250.68
Molecular FormulaC12H11ClN2O2

What is the molecular weight of Lenvatinib Impurity 18?

The molecular weight of Lenvatinib Impurity 18 is 250.68.

What is the molecular formula of Lenvatinib Impurity 18?

The molecular formula of Lenvatinib Impurity 18 is C12H11ClN2O2.

What is the chemical structure of Lenvatinib Impurity 18 based on its molecular formula?

The chemical structure of Lenvatinib Impurity 18 based on its molecular formula consists of 12 carbon atoms, 11 hydrogen atoms, 1 chlorine atom, 2 nitrogen atoms, and 2 oxygen atoms.

How is Lenvatinib Impurity 18 classified based on its molecular formula?

Lenvatinib Impurity 18 is classified as an organic compound based on its molecular formula.

What are the potential impurities that may be present in Lenvatinib Impurity 18?

The potential impurities that may be present in Lenvatinib Impurity 18 include other organic compounds with similar molecular weights and formulas.

How is Lenvatinib Impurity 18 different from Lenvatinib in terms of molecular structure?

Lenvatinib Impurity 18 differs from Lenvatinib in terms of its specific chemical composition and arrangement of atoms.

How does the molecular weight of Lenvatinib Impurity 18 impact its stability and reactivity?

The molecular weight of Lenvatinib Impurity 18 may impact its stability and reactivity, with heavier molecules potentially exhibiting different chemical behavior.

What are the properties of Lenvatinib Impurity 18 that make it suitable for pharmaceutical use?

The specific properties of Lenvatinib Impurity 18, such as its molecular weight and formula, may make it suitable for use in pharmaceutical applications.

How is Lenvatinib Impurity 18 typically synthesized in the laboratory?

Lenvatinib Impurity 18 may be synthesized in the laboratory through organic synthesis methods based on its known molecular formula.

What tests are commonly used to identify and quantify Lenvatinib Impurity 18 in pharmaceutical samples?

Analytical techniques such as mass spectrometry and chromatography may be used to identify and quantify Lenvatinib Impurity 18 in pharmaceutical samples.

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