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Fosfluconazole Impurity D

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For Research Use Only | Not For Clinical Use
CATAPB08053
Molecular Weight368.26
Molecular FormulaC13H14FN6O4P

What is the molecular weight of Fosfluconazole Impurity D?

The molecular weight of Fosfluconazole Impurity D is 368.26.

What is the molecular formula of Fosfluconazole Impurity D?

The molecular formula of Fosfluconazole Impurity D is C13H14FN6O4P.

What is the chemical structure of Fosfluconazole Impurity D?

The chemical structure of Fosfluconazole Impurity D is composed of carbon, hydrogen, fluorine, nitrogen, oxygen, and phosphorus atoms.

How does Fosfluconazole Impurity D differ from pure Fosfluconazole?

Fosfluconazole Impurity D likely contains impurities or by-products that are not found in pure Fosfluconazole.

What potential effects could impurities in Fosfluconazole Impurity D have on its use in pharmaceuticals?

Impurities in Fosfluconazole Impurity D could affect the efficacy, safety, and stability of the pharmaceutical product it is being used in.

How is Fosfluconazole Impurity D synthesized?

The synthesis of Fosfluconazole Impurity D likely involves the reaction of various starting materials to produce the final compound.

What analytical techniques can be used to detect and quantify Fosfluconazole Impurity D?

Analytical techniques such as HPLC (High Performance Liquid Chromatography) and spectroscopy may be used to detect and quantify Fosfluconazole Impurity D.

What are the potential risks associated with the presence of impurities in pharmaceutical products?

Impurities in pharmaceutical products can pose risks such as reduced efficacy, adverse reactions, and regulatory non-compliance.

How can impurities in pharmaceutical products be controlled and minimized?

Impurities in pharmaceutical products can be controlled and minimized through strict process control, quality assurance measures, and thorough analytical testing.

Why is it important for pharmaceutical manufacturers to identify and characterize impurities in their products?

Identifying and characterizing impurities in pharmaceutical products is important for ensuring product quality, safety, and regulatory compliance.

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