Faropenem Impurity 32

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For Research Use Only | Not For Clinical Use

CAT	APB07972
Molecular Weight	339.29
Molecular Formula	C12H14NNaO7S

What is the molecular weight of Faropenem Impurity 32?

The molecular weight of Faropenem Impurity 32 is 339.29.

What is the molecular formula of Faropenem Impurity 32?

The molecular formula of Faropenem Impurity 32 is C12H14NNaO7S.

How many carbon atoms are present in the molecular formula of Faropenem Impurity 32?

There are 12 carbon atoms present in the molecular formula of Faropenem Impurity 32.

What is the significance of the sodium (Na) atom in the molecular formula of Faropenem Impurity 32?

The presence of the sodium atom in the molecular formula of Faropenem Impurity 32 indicates the presence of a sodium ion in the compound.

How many hydrogen atoms are present in the molecular formula of Faropenem Impurity 32?

There are 14 hydrogen atoms present in the molecular formula of Faropenem Impurity 32.

What functional groups are present in the molecular formula of Faropenem Impurity 32?

The molecular formula of Faropenem Impurity 32 contains nitrogen, sulfur, oxygen, and sodium atoms, indicating the presence of corresponding functional groups.

What is the role of impurities in pharmaceutical compounds like Faropenem Impurity 32?

Impurities in pharmaceutical compounds like Faropenem Impurity 32 can affect the purity, safety, and efficacy of the final product, hence they need to be identified and controlled.

How is Faropenem Impurity 32 typically characterized and analyzed in pharmaceutical manufacturing?

Faropenem Impurity 32 is typically characterized and analyzed using techniques such as spectroscopy, chromatography, and mass spectrometry.

What is the importance of accurate identification and quantification of Faropenem Impurity 32 in pharmaceutical quality control?

Accurate identification and quantification of Faropenem Impurity 32 in pharmaceutical quality control are crucial for ensuring the safety and efficacy of the final product.

How can the presence of impurities like Faropenem Impurity 32 be minimized during the synthesis and production of pharmaceuticals?

The presence of impurities like Faropenem Impurity 32 can be minimized during the synthesis and production of pharmaceuticals by employing stringent quality control measures, purification techniques, and adherence to Good Manufacturing Practices (GMP).

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