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Crisaborole Impurity 58

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For Research Use Only | Not For Clinical Use
CATAPB04554
Synonyms4-(3-bromo-2-(hydroxymethyl)phenoxy)benzonitrile
Molecular Weight304.14
Molecular FormulaC14H10BrNO2

What is the molecular weight of Crisaborole Impurity 58?

The molecular weight of Crisaborole Impurity 58 is 304.14.

What is the molecular formula of Crisaborole Impurity 58?

The molecular formula of Crisaborole Impurity 58 is C14H10BrNO2.

What is an other name for Crisaborole Impurity 58?

An other name for Crisaborole Impurity 58 is 4-(3-bromo-2-(hydroxymethyl)phenoxy)benzonitrile.

What are the synonyms of Crisaborole Impurity 58?

One of the synonyms is 4-(3-bromo-2-(hydroxymethyl)phenoxy)benzonitrile.

What is the chemical structure of Crisaborole Impurity 58?

The chemical structure of Crisaborole Impurity 58 is a benzene ring with a bromine atom, hydroxymethyl group, and nitrile group attached.

How many carbon atoms are present in the molecular formula of Crisaborole Impurity 58?

There are 14 carbon atoms present in the molecular formula of Crisaborole Impurity 58.

What is the role of Crisaborole Impurity 58 in pharmaceutical products?

Crisaborole Impurity 58 is a specific impurity that needs to be monitored and controlled in pharmaceutical products containing Crisaborole.

How does the presence of Crisaborole Impurity 58 affect the quality of pharmaceutical products?

The presence of Crisaborole Impurity 58 in pharmaceutical products can impact the effectiveness and safety of the medication, leading to potential side effects or reduced efficacy.

What methods are used to detect and measure Crisaborole Impurity 58 in pharmaceutical formulations?

Analytical techniques such as HPLC (High Performance Liquid Chromatography) or mass spectrometry are commonly used to detect and quantify Crisaborole Impurity 58 in pharmaceutical formulations.

Why is it important to closely monitor the levels of Crisaborole Impurity 58 in pharmaceutical products?

Monitoring the levels of Crisaborole Impurity 58 is crucial to ensure the safety, efficacy, and compliance of pharmaceutical products as per regulatory standards and quality control measures.

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