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Lenvatinib Impurity 51

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For Research Use Only | Not For Clinical Use
CATAPB848133879
CAS848133-87-9
Molecular Weight247.68
Molecular FormulaC12H10ClN3O

What is the molecular weight of Lenvatinib Impurity 51?

The molecular weight of Lenvatinib Impurity 51 is 247.68.

What is the molecular formula of Lenvatinib Impurity 51?

The molecular formula of Lenvatinib Impurity 51 is C12H10ClN3O.

What is the CAS number of Lenvatinib Impurity 51?

The CAS number of Lenvatinib Impurity 51 is 848133-87-9.

What is the chemical structure of Lenvatinib Impurity 51?

The chemical structure of Lenvatinib Impurity 51 consists of carbon, hydrogen, chlorine, nitrogen, and oxygen atoms.

What is the significance of identifying Lenvatinib Impurity 51 in pharmaceutical products?

Identifying Lenvatinib Impurity 51 is crucial for quality control and ensuring the safety and effectiveness of pharmaceutical products.

How is Lenvatinib Impurity 51 typically detected and quantified in pharmaceutical samples?

Lenvatinib Impurity 51 is often detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry.

What are the potential sources of Lenvatinib Impurity 51 in pharmaceutical manufacturing?

Lenvatinib Impurity 51 can be formed as a byproduct during the synthesis or degradation of the active pharmaceutical ingredient (API) Lenvatinib.

How can the presence of Lenvatinib Impurity 51 impact the stability of pharmaceutical formulations?

The presence of Lenvatinib Impurity 51 can affect the stability, potency, and safety of pharmaceutical formulations, leading to potential quality control issues.

Are there specific regulations or guidelines regarding the acceptable levels of Lenvatinib Impurity 51 in pharmaceutical products?

Regulatory authorities such as the FDA and EMA may provide guidelines on acceptable levels of Lenvatinib Impurity 51 in pharmaceutical products to ensure patient safety.

How can the identification and control of Lenvatinib Impurity 51 contribute to the overall quality assurance of pharmaceutical products?

By accurately identifying and controlling Lenvatinib Impurity 51, pharmaceutical manufacturers can maintain the integrity and efficacy of their products, ultimately enhancing patient outcomes and regulatory compliance.

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