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Apremilast Impurity A

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For Research Use Only | Not For Clinical Use
CATAPB06679
Molecular Weight273.35
Molecular FormulaC12H19NO4S

What is the molecular weight of Apremilast Impurity A?

The molecular weight of Apremilast Impurity A is 273.35.

What is the molecular formula of Apremilast Impurity A?

The molecular formula of Apremilast Impurity A is C12H19NO4S.

What are the elements present in the molecular formula of Apremilast Impurity A?

The elements present in the molecular formula of Apremilast Impurity A are carbon, hydrogen, nitrogen, oxygen, and sulfur.

How many carbon atoms are present in the molecular formula of Apremilast Impurity A?

There are 12 carbon atoms present in the molecular formula of Apremilast Impurity A.

What is the significance of Apremilast Impurity A in pharmaceuticals?

Apremilast Impurity A is a pharmaceutical impurity that can affect the efficacy and safety of Apremilast, a medication used to treat certain skin conditions and arthritis.

How is Apremilast Impurity A synthesized?

Apremilast Impurity A can be synthesized using organic chemistry methods to create a compound with the specific molecular formula of C12H19NO4S.

What potential side effects or interactions should be monitored when using Apremilast Impurity A in pharmaceutical products?

When using Apremilast Impurity A in pharmaceutical products, potential side effects or interactions should be monitored to ensure the safety and efficacy of the medication.

Are there any regulatory guidelines for the presence of Apremilast Impurity A in pharmaceutical products?

Regulatory guidelines may specify maximum acceptable levels of Apremilast Impurity A in pharmaceutical products to ensure product quality and safety.

How does the presence of Apremilast Impurity A impact the stability of pharmaceutical formulations?

The presence of Apremilast Impurity A in pharmaceutical formulations may impact the stability and shelf life of the product, requiring careful monitoring and control during the manufacturing process.

What analytical methods can be used to detect and quantify Apremilast Impurity A in pharmaceutical products?

Analytical techniques such as chromatography, spectroscopy, and mass spectrometry can be used to detect and quantify Apremilast Impurity A in pharmaceutical products for quality control purposes.

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