Erlotinib Impurity 55

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For Research Use Only | Not For Clinical Use

CAT	APB05327
Synonyms	potassium 5-(ethoxycarbonyl)-2-(2-methoxyethoxy)phenolate
Molecular Weight	278.34
Molecular Formula	C12H15KO5

What is the chemical name of Erlotinib Impurity 55?

The chemical name of Erlotinib Impurity 55 is potassium 5-(ethoxycarbonyl)-2-(2-methoxyethoxy)phenolate.

What is the molecular weight of Erlotinib Impurity 55?

The molecular weight of Erlotinib Impurity 55 is 278.34 g/mol.

What is the molecular formula of Erlotinib Impurity 55?

The molecular formula of Erlotinib Impurity 55 is C12H15KO5.

What are some synonyms for Erlotinib Impurity 55?

One of the synonyms is potassium 5-(ethoxycarbonyl)-2-(2-methoxyethoxy)phenolate.

What is the IUPAC name of Erlotinib Impurity 55?

The IUPAC name of Erlotinib Impurity 55 is potassium 5-(ethoxycarbonyl)-2-(2-methoxyethoxy)phenolate.

What is the structure of Erlotinib Impurity 55?

The structure of Erlotinib Impurity 55 consists of a phenolate ring attached to a 5-(ethoxycarbonyl)-2-(2-methoxyethoxy) group, with a potassium atom.

How many carbon atoms are present in the molecular formula of Erlotinib Impurity 55?

There are 12 carbon atoms present in the molecular formula of Erlotinib Impurity 55.

What is the role of Erlotinib Impurity 55 in pharmaceutical processes?

Erlotinib Impurity 55 is a specific impurity that needs to be controlled and monitored in pharmaceutical processes involving Erlotinib to ensure product quality and safety.

How is Erlotinib Impurity 55 typically detected and quantified in pharmaceutical samples?

Erlotinib Impurity 55 is typically detected and quantified using analytical techniques such as HPLC (High Performance Liquid Chromatography) and mass spectrometry.

Why is it important to characterize Erlotinib Impurity 55 in pharmaceutical formulations?

Characterizing Erlotinib Impurity 55 in pharmaceutical formulations is important for regulatory compliance, quality control, and to ensure the efficacy and safety of the final drug product.

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