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Enzalutamide Impurity 50

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For Research Use Only | Not For Clinical Use
CATAPB05429
Synonyms2-((4-carbamoyl-3-fluorophenyl)amino)-2-methylpropanoic acid
Molecular Weight240.23
Molecular FormulaC11H13FN2O3

What is the molecular weight of Enzalutamide Impurity 50?

The molecular weight of Enzalutamide Impurity 50 is 240.23.

What is the molecular formula of Enzalutamide Impurity 50?

The molecular formula of Enzalutamide Impurity 50 is C11H13FN2O3.

What are some synonyms for Enzalutamide Impurity 50?

One synonym for Enzalutamide Impurity 50 is 2-((4-carbamoyl-3-fluorophenyl)amino)-2-methylpropanoic acid.

Can Enzalutamide Impurity 50 be used as an active ingredient in medication?

No, Enzalutamide Impurity 50 is an impurity and not an active ingredient in medication.

How is Enzalutamide Impurity 50 typically produced?

Enzalutamide Impurity 50 is typically produced as a byproduct during the manufacturing process of enzalutamide.

Is Enzalutamide Impurity 50 a commonly found impurity in enzalutamide products?

Enzalutamide Impurity 50 is not a commonly found impurity in enzalutamide products.

What are the potential effects of Enzalutamide Impurity 50 in pharmaceutical products?

The presence of Enzalutamide Impurity 50 in pharmaceutical products may affect the purity and effectiveness of the medication.

How is the purity of pharmaceutical products containing Enzalutamide Impurity 50 monitored?

The purity of pharmaceutical products containing Enzalutamide Impurity 50 is monitored through rigorous quality control processes and testing.

Are there regulations in place regarding the acceptable levels of Enzalutamide Impurity 50 in pharmaceutical products?

Yes, regulatory agencies have established limits on the acceptable levels of Enzalutamide Impurity 50 in pharmaceutical products.

What steps can be taken to minimize the presence of Enzalutamide Impurity 50 in pharmaceutical products?

Manufacturers can implement strict quality control measures and purification techniques to minimize the presence of Enzalutamide Impurity 50 in pharmaceutical products.

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