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Faropenem Impurity 1

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For Research Use Only | Not For Clinical Use
CATAPB07962
Molecular Weight323.3
Molecular FormulaC12H14NNaO6S

What is the molecular weight of Faropenem Impurity 1?

The molecular weight of Faropenem Impurity 1 is 323.3.

What is the molecular formula of Faropenem Impurity 1?

The molecular formula of Faropenem Impurity 1 is C12H14NNaO6S.

How many carbon atoms are present in the molecular formula of Faropenem Impurity 1?

There are 12 carbon atoms in the molecular formula of Faropenem Impurity 1.

What other elements are present in the molecular formula of Faropenem Impurity 1?

The molecular formula of Faropenem Impurity 1 also contains hydrogen, nitrogen, sodium, oxygen, and sulfur.

What is the chemical structure of Faropenem Impurity 1 based on its molecular formula?

The chemical structure of Faropenem Impurity 1 based on its molecular formula consists of 12 carbon atoms, 14 hydrogen atoms, 1 nitrogen atom, 1 sodium atom, 6 oxygen atoms, and 1 sulfur atom.

How is Faropenem Impurity 1 related to the drug Faropenem?

Faropenem Impurity 1 is a substance that is related to or derived from the drug Faropenem.

Why is it important to identify and characterize impurities like Faropenem Impurity 1 in pharmaceutical substances?

It is important to identify and characterize impurities like Faropenem Impurity 1 in pharmaceutical substances to ensure the safety, efficacy, and quality of the final drug product.

Can Faropenem Impurity 1 affect the bioavailability of the drug Faropenem?

Yes, impurities like Faropenem Impurity 1 can potentially affect the bioavailability of the drug Faropenem.

How is Faropenem Impurity 1 typically identified and quantified in pharmaceutical samples?

Faropenem Impurity 1 is typically identified and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) and mass spectrometry.

What measures can be taken to minimize the presence of impurities like Faropenem Impurity 1 in pharmaceutical production?

To minimize the presence of impurities like Faropenem Impurity 1 in pharmaceutical production, manufacturers can implement strict quality control measures, use high-quality starting materials, and optimize manufacturing processes.

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