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Nifuzide EP impurity D

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For Research Use Only | Not For Clinical Use
CATAPB112537969
CAS112537-96-9
Molecular Weight278.18
Molecular FormulaC10H6N4O6

What is the product name of CAS 112537-96-9?

The product name is Nifuzide EP impurity D.

What is the molecular weight of Nifuzide EP impurity D?

The molecular weight is 278.18.

What is the molecular formula of Nifuzide EP impurity D?

The molecular formula is C10H6N4O6.

What does the "EP" in Nifuzide EP impurity D stand for?

The "EP" likely stands for "European Pharmacopoeia."

What is the significance of impurities in pharmaceutical products?

Impurities in pharmaceutical products can affect the quality, efficacy, and safety of the medication.

How is Nifuzide EP impurity D detected and quantified in pharmaceutical products?

Nifuzide EP impurity D can be detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry.

Why is it important to control impurities in pharmaceutical products?

Controlling impurities is crucial to ensure the safety and efficacy of pharmaceutical products for patient use.

What are some common sources of impurities in pharmaceutical manufacturing?

Impurities can come from starting materials, reagents, by-products of reactions, and degradation of the active pharmaceutical ingredient.

How can the presence of Nifuzide EP impurity D impact the stability of a pharmaceutical product?

The presence of impurities like Nifuzide EP impurity D can contribute to the degradation of the active ingredient, potentially reducing the overall stability of the product.

What steps can be taken to minimize the presence of impurities like Nifuzide EP impurity D in pharmaceutical products?

Manufacturers can implement rigorous quality control measures, use high-quality starting materials, optimize manufacturing processes, and conduct thorough analytical testing to minimize impurities in pharmaceutical products.

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