Enzalutamide impurity H

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For Research Use Only | Not For Clinical Use

CAT	APB05317
Synonyms	methyl 2-methyl-2-((4-(methylcarbamoyl)phenyl)amino)propanoate
Molecular Weight	250.29
Molecular Formula	C13H18N2O3

What is the molecular weight of Enzalutamide impurity H?

The molecular weight of Enzalutamide impurity H is 250.29.

What is the molecular formula of Enzalutamide impurity H?

The molecular formula of Enzalutamide impurity H is C13H18N2O3.

What are the synonyms for Enzalutamide impurity H?

One of the synonyms is methyl 2-methyl-2-((4-(methylcarbamoyl)phenyl)amino)propanoate.

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

There are 13 carbon atoms present in the molecular formula of Enzalutamide impurity H.

What is the chemical structure of Enzalutamide impurity H?

The chemical structure of Enzalutamide impurity H consists of a phenyl group connected to a carbamoyl group attached to a propanoate group.

What is the significance of Enzalutamide impurity H in the pharmaceutical industry?

Enzalutamide impurity H is important in the pharmaceutical industry as it is a specific molecule that needs to be characterized and controlled in the production of enzalutamide.

How is Enzalutamide impurity H detected and quantified in pharmaceutical products?

Enzalutamide impurity H is detected and quantified using analytical techniques such as chromatography and spectroscopy.

Can Enzalutamide impurity H affect the efficacy or safety of enzalutamide?

Yes, Enzalutamide impurity H can potentially affect the efficacy or safety of enzalutamide, which is why it is important to control impurity levels.

What are the potential sources of Enzalutamide impurity H in the manufacturing process?

Enzalutamide impurity H can be formed as a byproduct or degradation product during the synthesis or storage of enzalutamide.

How does the presence of Enzalutamide impurity H impact the quality control of pharmaceutical products?

The presence of Enzalutamide impurity H requires strict quality control measures to ensure that the final pharmaceutical product meets regulatory standards for purity and safety.

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