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Cefprozil EP Impurity F

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For Research Use Only | Not For Clinical Use
CATAPB04481
Synonyms(6R,7R)-7-amino-8-oxo-3-((E)-prop-1-en-1-yl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Molecular Weight240.28
Molecular FormulaC10H12N2O3S

What is the molecular weight of Cefprozil EP Impurity F?

The molecular weight of Cefprozil EP Impurity F is 240.28.

What is the molecular formula of Cefprozil EP Impurity F?

The molecular formula of Cefprozil EP Impurity F is C10H12N2O3S.

What are some synonyms for Cefprozil EP Impurity F?

One synonym for Cefprozil EP Impurity F is (6R,7R)-7-amino-8-oxo-3-((E)-prop-1-en-1-yl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid.

What is the chemical structure of Cefprozil EP Impurity F?

The chemical structure of Cefprozil EP Impurity F can be described by the molecular formula C10H12N2O3S.

What functional groups are present in Cefprozil EP Impurity F?

Cefprozil EP Impurity F contains an amino group, an oxo group, an alkene group, and a carboxylic acid group.

Can Cefprozil EP Impurity F be used as an antibiotic?

Cefprozil EP Impurity F is not used as an antibiotic itself, but it is an impurity often found in pharmaceutical formulations of Cefprozil.

How is Cefprozil EP Impurity F typically formed?

Cefprozil EP Impurity F is typically formed as a byproduct during the synthesis or degradation of Cefprozil.

What is the significance of identifying and quantifying Cefprozil EP Impurity F in pharmaceutical products?

Identifying and quantifying Cefprozil EP Impurity F is important for ensuring the quality, safety, and efficacy of pharmaceutical products containing Cefprozil.

Is Cefprozil EP Impurity F considered harmful in pharmaceuticals?

The presence of Cefprozil EP Impurity F in pharmaceuticals is generally considered undesirable, as impurities can affect the stability and effectiveness of the drug.

How can the presence of Cefprozil EP Impurity F be minimized in pharmaceutical production?

The presence of Cefprozil EP Impurity F can be minimized through careful purification and quality control processes during pharmaceutical production.

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