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Erlotinib Impurity 36

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For Research Use Only | Not For Clinical Use
CATAPB05343
Synonyms7-(2-hydroxyethoxy)-6-(2-methoxyethoxy)quinazolin-4(3H)-one
Molecular Weight280.28
Molecular FormulaC13H16N2O5

What is the molecular weight of Erlotinib Impurity 36?

The molecular weight of Erlotinib Impurity 36 is 280.28.

What is the molecular formula of Erlotinib Impurity 36?

The molecular formula of Erlotinib Impurity 36 is C13H16N2O5.

What are the synonyms for Erlotinib Impurity 36?

One of the synonyms is 7-(2-hydroxyethoxy)-6-(2-methoxyethoxy)quinazolin-4(3H)-one.

How many carbons are present in the molecular formula of Erlotinib Impurity 36?

There are 13 carbon atoms present in the molecular formula of Erlotinib Impurity 36.

What is the chemical structure of Erlotinib Impurity 36?

The chemical structure of Erlotinib Impurity 36 is a quinazolin-4(3H)-one derivative with hydroxyethoxy and methoxyethoxy substitutions.

What is the role of Erlotinib Impurity 36 in pharmaceuticals?

Erlotinib Impurity 36 is a known impurity in the pharmaceutical compound Erlotinib.

What is the significance of identifying Erlotinib Impurity 36 in pharmaceutical manufacturing?

Identifying Erlotinib Impurity 36 is important for quality control and regulatory compliance in pharmaceutical manufacturing.

How is Erlotinib Impurity 36 detected in pharmaceutical products?

Erlotinib Impurity 36 can be detected using analytical techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry.

What are the potential risks associated with the presence of Erlotinib Impurity 36 in pharmaceuticals?

Erlotinib Impurity 36 may affect the purity and stability of the pharmaceutical product, leading to potential safety concerns for patients.

How can pharmaceutical companies mitigate the presence of Erlotinib Impurity 36 in their products?

Pharmaceutical companies can establish strict quality control measures and analytical testing protocols to reduce the levels of Erlotinib Impurity 36 in their products.

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