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Flucloxacillin EP Impurity D

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For Research Use Only | Not For Clinical Use
CATAPB3919742
CAS3919-74-2
Structure
Molecular Weight255.63
Molecular FormulaC11H7ClFNO3

What is the product name of CAS 3919-74-2?

The product name is Flucloxacillin EP Impurity D.

What is the molecular weight of Flucloxacillin EP Impurity D?

The molecular weight is 255.63.

What is the molecular formula of Flucloxacillin EP Impurity D?

The molecular formula is C11H7ClFNO3.

What is the chemical structure of Flucloxacillin EP Impurity D?

The chemical structure is composed of atoms of carbon, hydrogen, chlorine, fluorine, nitrogen, and oxygen.

Is Flucloxacillin EP Impurity D a pure substance?

No, Flucloxacillin EP Impurity D is an impurity of Flucloxacillin EP.

What is the significance of identifying Flucloxacillin EP Impurity D in pharmaceutical products?

Identifying impurities is important for quality control and ensuring the safety and efficacy of pharmaceutical products.

How is Flucloxacillin EP Impurity D distinguished from the main drug Flucloxacillin EP?

Flucloxacillin EP Impurity D may have a different molecular structure or properties compared to the main drug Flucloxacillin EP.

What methods are used to detect and quantify Flucloxacillin EP Impurity D in pharmaceutical formulations?

Techniques such as chromatography, spectroscopy, and mass spectrometry can be used to analyze impurities in pharmaceuticals.

Can impurities like Flucloxacillin EP Impurity D affect the stability or effectiveness of a medication?

Yes, impurities can potentially impact the stability, efficacy, and safety of medications, which is why they are closely monitored and controlled.

How can pharmaceutical manufacturers ensure that levels of Flucloxacillin EP Impurity D are within acceptable limits in their products?

Manufacturers can implement rigorous quality control measures, conduct thorough testing and analysis, and adhere to regulatory guidelines to ensure impurity levels are within acceptable limits.

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