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Marbofloxacin EP Impurity A

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For Research Use Only | Not For Clinical Use
CATAPB115551401
CAS115551-40-1
Molecular Weight270.19
Molecular FormulaC11H8F2N2O4

What is the name of the impurity referred to in the product?

The impurity is called Marbofloxacin EP Impurity A.

What is the Chemical Abstracts Service (CAS) number for Marbofloxacin EP Impurity A?

The CAS number for Marbofloxacin EP Impurity A is 115551-40-1.

What is the molecular weight of Marbofloxacin EP Impurity A?

The molecular weight of Marbofloxacin EP Impurity A is 270.19.

What is the molecular formula of Marbofloxacin EP Impurity A?

The molecular formula of Marbofloxacin EP Impurity A is C11H8F2N2O4.

How many atoms are present in the molecular formula of Marbofloxacin EP Impurity A?

There are a total of 25 atoms present in the molecular formula of C11H8F2N2O4.

What is the significance of Marbofloxacin EP Impurity A in pharmaceuticals?

Marbofloxacin EP Impurity A is an impurity that may need to be identified and quantified as part of the quality control process in pharmaceutical manufacturing.

How is Marbofloxacin EP Impurity A typically detected and analyzed?

Marbofloxacin EP Impurity A is typically detected and analyzed using analytical techniques such as chromatography or spectroscopy.

Why is it important to identify and control impurities like Marbofloxacin EP Impurity A in pharmaceutical products?

Impurities in pharmaceutical products can impact the efficacy, safety, and quality of the drug, so controlling and monitoring impurities is crucial for ensuring product quality.

Are there regulatory guidelines or limits for impurities like Marbofloxacin EP Impurity A in pharmaceutical products?

Yes, regulatory authorities like the FDA and EMA have guidelines and limits for impurities in pharmaceutical products to ensure patient safety.

What steps can be taken to minimize the presence of impurities like Marbofloxacin EP Impurity A during pharmaceutical manufacturing?

Steps to minimize impurities during manufacturing include using high-quality raw materials, optimizing production processes, and implementing robust quality control measures.

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