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Cefprozil EP Impurity D

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For Research Use Only | Not For Clinical Use
CATAPB04522
Synonyms(6R,7R)-7-amino-8-oxo-3-((Z)-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 synonym for Cefprozil EP Impurity D?

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

What is the molecular weight of Cefprozil EP Impurity D?

The molecular weight of Cefprozil EP Impurity D is 240.28.

What is the molecular formula of Cefprozil EP Impurity D?

The molecular formula of Cefprozil EP Impurity D is C10H12N2O3S.

What are the atoms present in the molecular formula of Cefprozil EP Impurity D?

The atoms present in the molecular formula of Cefprozil EP Impurity D are carbon (C), hydrogen (H), nitrogen (N), oxygen (O), and sulfur (S).

What is the structure of Cefprozil EP Impurity D?

Cefprozil EP Impurity D has a bicyclic structure with a carboxylic acid functional group.

How many total atoms are present in the molecular formula of Cefprozil EP Impurity D?

There are a total of 17 atoms present in the molecular formula of Cefprozil EP Impurity D.

What is the significance of the (Z)-prop-1-en-1-yl group in the synonym of Cefprozil EP Impurity D?

The (Z)-prop-1-en-1-yl group in the synonym of Cefprozil EP Impurity D indicates the presence of a double bond in the carbon chain.

In what pharmaceutical context is Cefprozil EP Impurity D relevant?

Cefprozil EP Impurity D is relevant in the pharmaceutical context as an impurity that may be present in Cefprozil formulations.

How is Cefprozil EP Impurity D typically characterized and identified in pharmaceutical formulations?

Cefprozil EP Impurity D is typically characterized and identified through analytical techniques such as HPLC (High Performance Liquid Chromatography) and mass spectrometry.

What is the role of understanding impurities like Cefprozil EP Impurity D in pharmaceutical quality control?

Understanding impurities like Cefprozil EP Impurity D is crucial for pharmaceutical quality control to ensure the safety, efficacy, and stability of drug products.

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