Faropenem Impurity 35

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For Research Use Only | Not For Clinical Use

CAT	APB07971
Molecular Weight	347.29
Molecular Formula	C12H15NNa2O6S

What is the molecular weight of Faropenem Impurity 35?

The molecular weight of Faropenem Impurity 35 is 347.29.

What is the molecular formula of Faropenem Impurity 35?

The molecular formula of Faropenem Impurity 35 is C12H15NNa2O6S.

What is the specific role of Faropenem Impurity 35 in pharmaceuticals?

The specific role of Faropenem Impurity 35 in pharmaceuticals is as an impurity in the production of faropenem.

How is Faropenem Impurity 35 classified chemically?

Faropenem Impurity 35 is classified as a sodium salt derivative with specific molecular structure.

Can Faropenem Impurity 35 be used as an active ingredient in medications?

Faropenem Impurity 35 is not used as an active ingredient in medications, as it is classified as an impurity.

What are the potential effects of having Faropenem Impurity 35 present in a pharmaceutical product?

Having Faropenem Impurity 35 present in a pharmaceutical product can impact the purity and efficacy of the final drug product.

How is Faropenem Impurity 35 typically removed or reduced in pharmaceutical manufacturing processes?

Faropenem Impurity 35 is typically removed or reduced through various purification techniques during pharmaceutical manufacturing processes.

Are there any standards or limits set for the acceptable levels of Faropenem Impurity 35 in pharmaceutical products?

Yes, there are regulatory standards and limits set for the acceptable levels of Faropenem Impurity 35 in pharmaceutical products to ensure safety and quality.

What are some common methods of analyzing and detecting the presence of Faropenem Impurity 35 in pharmaceutical products?

Common methods of analyzing and detecting the presence of Faropenem Impurity 35 include chromatography, spectroscopy, and mass spectrometry.

How does the presence of Faropenem Impurity 35 in pharmaceutical products impact product stability and storage conditions?

The presence of Faropenem Impurity 35 in pharmaceutical products can affect product stability and may require specific storage conditions to maintain drug quality over time.

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