Enzalutamide impurity G

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For Research Use Only | Not For Clinical Use

CAT	APB05318
Synonyms	2-methyl-2-((4-(methylcarbamoyl)phenyl)amino)propanoic acid
Molecular Weight	236.27
Molecular Formula	C12H16N2O3

What is the molecular weight of Enzalutamide impurity G?

The molecular weight of Enzalutamide impurity G is 236.27.

What is the molecular formula of Enzalutamide impurity G?

The molecular formula of Enzalutamide impurity G is C12H16N2O3.

What are some synonyms for Enzalutamide impurity G?

Some synonyms for Enzalutamide impurity G include 2-methyl-2-((4-(methylcarbamoyl)phenyl)amino)propanoic acid.

What is the chemical structure of Enzalutamide impurity G?

The chemical structure of Enzalutamide impurity G is C12H16N2O3.

How many carbon atoms are present in the molecular formula of Enzalutamide impurity G?

There are 12 carbon atoms present in the molecular formula of Enzalutamide impurity G.

What is the total number of atoms in the molecular formula of Enzalutamide impurity G?

The total number of atoms in the molecular formula of Enzalutamide impurity G is 33 (12 carbon atoms, 16 hydrogen atoms, 2 nitrogen atoms, and 3 oxygen atoms).

What functional groups are present in the structure of Enzalutamide impurity G?

The structure of Enzalutamide impurity G contains an amide group and a methyl group.

How does the molecular weight of Enzalutamide impurity G compare to the molecular weight of the parent compound Enzalutamide?

The molecular weight of Enzalutamide impurity G is lower than the molecular weight of the parent compound Enzalutamide, which has a molecular weight of 464.83.

Can Enzalutamide impurity G be considered a derivative of Enzalutamide?

Yes, Enzalutamide impurity G can be considered a derivative of Enzalutamide due to the structural similarity between the two compounds.

What is the significance of identifying and characterizing impurities like Enzalutamide impurity G in pharmaceuticals?

Identifying and characterizing impurities like Enzalutamide impurity G is important in ensuring the quality, safety, and efficacy of pharmaceutical products. By understanding and controlling impurities, manufacturers can improve the overall quality of the drug product.

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