Cabozantinib impurity 39

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For Research Use Only | Not For Clinical Use

CAT	APB04115
Synonyms	6,7-dimethoxy-N,N-dimethylquinolin-4-amine
Molecular Weight	232.28
Molecular Formula	C13H16N2O2

What is the chemical name of Cabozantinib impurity 39?

The chemical name of Cabozantinib impurity 39 is 6,7-dimethoxy-N,N-dimethylquinolin-4-amine.

What is the molecular weight of Cabozantinib impurity 39?

The molecular weight of Cabozantinib impurity 39 is 232.28.

Can you provide the molecular formula of Cabozantinib impurity 39?

The molecular formula of Cabozantinib impurity 39 is C13H16N2O2.

What is the structure of Cabozantinib impurity 39?

The structure of Cabozantinib impurity 39 consists of a quinoline ring with two methoxy and two dimethyl amine groups.

How does Cabozantinib impurity 39 differ from Cabozantinib?

The main difference is that Cabozantinib impurity 39 is a specific impurity of Cabozantinib, not the active ingredient itself.

Why is it important to identify and characterize impurities like Cabozantinib impurity 39?

Identifying and characterizing impurities in pharmaceutical products is crucial for ensuring product quality, safety, and efficacy.

How is Cabozantinib impurity 39 typically detected and quantified?

Cabozantinib impurity 39 is typically detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) and mass spectrometry.

Can Cabozantinib impurity 39 impact the effectiveness of Cabozantinib as a drug?

The presence of impurities like Cabozantinib impurity 39 can potentially impact the effectiveness and safety of the drug product, hence the importance of monitoring and controlling impurities.

Is Cabozantinib impurity 39 a common impurity found in Cabozantinib formulations?

Cabozantinib impurity 39 may or may not be a common impurity found in Cabozantinib formulations, depending on the manufacturing process and storage conditions.

How can pharmaceutical companies ensure that Cabozantinib impurity 39 levels are within acceptable limits?

Pharmaceutical companies can ensure that Cabozantinib impurity 39 levels are within acceptable limits by developing and validating analytical methods for impurity detection, monitoring impurity levels throughout the manufacturing process, and implementing stringent quality control measures.

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