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Melphalan EP lmpurity F

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For Research Use Only | Not For Clinical Use
CATAPB11383
Molecular Weight339.64
Molecular FormulaC13H17Cl3N2O2

What is the name of the product?

Melphalan EP Impurity F.

What is the molecular weight of Melphalan EP Impurity F?

The molecular weight of Melphalan EP Impurity F is 339.64.

What is the molecular formula of Melphalan EP Impurity F?

The molecular formula of Melphalan EP Impurity F is C13H17Cl3N2O2.

How is Melphalan EP Impurity F related to the compound Melphalan?

Melphalan EP Impurity F is an impurity associated with the compound Melphalan.

Why is it important to identify and quantify impurities like Melphalan EP Impurity F in pharmaceutical compounds?

It is important to identify and quantify impurities like Melphalan EP Impurity F in pharmaceutical compounds to ensure the safety and efficacy of the final product.

What methods are commonly used to detect impurities in pharmaceutical compounds?

Common methods used to detect impurities in pharmaceutical compounds include chromatography, spectroscopy, and mass spectrometry.

How can the presence of Melphalan EP Impurity F impact the quality of a pharmaceutical product?

The presence of Melphalan EP Impurity F can impact the quality of a pharmaceutical product by potentially affecting its stability, potency, and safety.

What are some potential sources of impurities like Melphalan EP Impurity F in pharmaceutical manufacturing?

Impurities like Melphalan EP Impurity F can arise from raw materials, solvents, reagents, and the manufacturing process itself in pharmaceutical manufacturing.

How is the level of impurities like Melphalan EP Impurity F regulated in pharmaceutical products?

Regulatory agencies set limits on impurities like Melphalan EP Impurity F in pharmaceutical products to ensure they are within acceptable safety and quality standards.

What steps can be taken to minimize the presence of impurities like Melphalan EP Impurity F in pharmaceutical products?

Measures such as improving manufacturing processes, using high-quality raw materials, and implementing rigorous quality control can help minimize the presence of impurities like Melphalan EP Impurity F in pharmaceutical products.

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