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Cefdinir Impurity G

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For Research Use Only | Not For Clinical Use
CATAPB04266
Synonyms(6R,7R)-7-((Z)-2-(2-aminothiazol-4-yl)-2-(hydroxyimino)acetamido)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Molecular Weight383.4
Molecular FormulaC13H13N5O5S2

What is the synonym for Cefdinir Impurity G?

The synonym for Cefdinir Impurity G is (6R,7R)-7-((Z)-2-(2-aminothiazol-4-yl)-2-(hydroxyimino)acetamido)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid.

What is the molecular weight of Cefdinir Impurity G?

The molecular weight of Cefdinir Impurity G is 383.4.

What is the molecular formula of Cefdinir Impurity G?

The molecular formula of Cefdinir Impurity G is C13H13N5O5S2.

What is the chemical structure of Cefdinir Impurity G based on its molecular formula?

The chemical structure of Cefdinir Impurity G based on its molecular formula is (6R,7R)-7-((Z)-2-(2-aminothiazol-4-yl)-2-(hydroxyimino)acetamido)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid.

What type of compound is Cefdinir Impurity G?

Cefdinir Impurity G is a thiazole compound.

What are the different elements present in the molecular formula of Cefdinir Impurity G?

The elements present in the molecular formula of Cefdinir Impurity G are carbon, hydrogen, nitrogen, oxygen, and sulfur.

Can Cefdinir Impurity G be used as an antibiotic?

Cefdinir Impurity G is an impurity and not the active pharmaceutical ingredient, so it is not used as an antibiotic.

Is Cefdinir Impurity G commercially available for purchase?

Yes, Cefdinir Impurity G is commercially available for purchase for research and reference purposes.

What is the significance of determining impurities like Cefdinir Impurity G in pharmaceutical products?

Determining impurities like Cefdinir Impurity G in pharmaceutical products is important for quality control, ensuring product purity and safety.

What are some analytical methods that can be used to detect Cefdinir Impurity G in pharmaceutical samples?

Analytical methods such as chromatography (e.g., HPLC), spectroscopy (e.g., NMR), and mass spectrometry can be used to detect Cefdinir Impurity G in pharmaceutical samples.

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