Lenvatinib Impurity 36

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For Research Use Only | Not For Clinical Use

CAT	APB08378
Molecular Weight	223.61
Molecular Formula	C10H6ClNO3

What is the molecular weight of Lenvatinib Impurity 36?

The molecular weight of Lenvatinib Impurity 36 is 223.61.

What is the molecular formula of Lenvatinib Impurity 36?

The molecular formula of Lenvatinib Impurity 36 is C10H6ClNO3.

What is the chemical structure of Lenvatinib Impurity 36 based on its molecular formula?

The chemical structure of Lenvatinib Impurity 36 consists of 10 carbon atoms, 6 hydrogen atoms, 1 chlorine atom, and 3 oxygen atoms.

How is Lenvatinib Impurity 36 related to the drug Lenvatinib?

Lenvatinib Impurity 36 is a chemical impurity that may be present in samples of the drug Lenvatinib.

Why is it important to identify and characterize impurities like Lenvatinib Impurity 36 in pharmaceutical products?

It is important to identify and characterize impurities like Lenvatinib Impurity 36 in pharmaceutical products to ensure the safety, quality, and efficacy of the drug.

How is Lenvatinib Impurity 36 typically detected and quantified in pharmaceutical samples?

Lenvatinib Impurity 36 is typically detected and quantified using analytical techniques such as chromatography and spectroscopy.

Are there regulatory guidelines for the acceptable levels of impurities, including Lenvatinib Impurity 36, in pharmaceutical products?

Yes, regulatory authorities like the FDA have guidelines on the acceptable limits of impurities in pharmaceutical products.

What are the potential risks associated with the presence of impurities like Lenvatinib Impurity 36 in pharmaceutical products?

The presence of impurities like Lenvatinib Impurity 36 may pose risks such as decreased efficacy, toxicity, or adverse reactions in patients.

How can pharmaceutical companies minimize the presence of impurities like Lenvatinib Impurity 36 in their products?

Pharmaceutical companies can minimize impurities by implementing strict quality control processes, using high-quality raw materials, and conducting thorough analytical testing.

What steps can be taken to remove or reduce impurities like Lenvatinib Impurity 36 during the manufacturing process of pharmaceutical products?

Steps to remove or reduce impurities like Lenvatinib Impurity 36 may include refining processes, purification techniques, and filtration methods.

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