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Crisaborole Impurity 17

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For Research Use Only | Not For Clinical Use
CATAPB01138
Synonyms3-(4-bromo-3-(hydroxymethyl)phenoxy)benzonitrile
Molecular Weight304.14
Molecular FormulaC14H10BrNO2

What is the molecular weight of Crisaborole Impurity 17?

The molecular weight of Crisaborole Impurity 17 is 304.14.

What is the molecular formula of Crisaborole Impurity 17?

The molecular formula of Crisaborole Impurity 17 is C14H10BrNO2.

What are the synonyms for Crisaborole Impurity 17?

One of the synonyms is 3-(4-bromo-3-(hydroxymethyl)phenoxy)benzonitrile.

What is the chemical structure of Crisaborole Impurity 17?

The chemical structure of Crisaborole Impurity 17 is C14H10BrNO2.

How many carbon atoms are present in the molecular formula of Crisaborole Impurity 17?

There are 14 carbon atoms present in the molecular formula of Crisaborole Impurity 17.

What is the role of Crisaborole Impurity 17 in pharmaceuticals?

Crisaborole Impurity 17 is typically considered an impurity in pharmaceuticals.

What functional groups are present in the chemical structure of Crisaborole Impurity 17?

The functional groups present in the chemical structure of Crisaborole Impurity 17 include a phenyl group, a bromine atom, a hydroxymethyl group, and a nitrile group.

What is the significance of identifying Crisaborole Impurity 17 in drug development?

Identifying Crisaborole Impurity 17 is important in drug development to ensure the purity and safety of pharmaceutical products.

How is Crisaborole Impurity 17 synthesized in the laboratory?

Crisaborole Impurity 17 can be synthesized in the laboratory through various chemical reactions involving starting materials containing phenol, bromine, and nitrile functional groups.

What measures are taken to control the presence of Crisaborole Impurity 17 in pharmaceutical formulations?

Quality control processes are implemented to monitor and control the presence of Crisaborole Impurity 17 in pharmaceutical formulations, ensuring compliance with regulatory standards.

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