Cefadroxil Impurity 10

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For Research Use Only | Not For Clinical Use

CAT	APB04435
Synonyms	(6R,7R)-7-((ethoxycarbonyl)amino)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Molecular Weight	286.3
Molecular Formula	C11H14N2O5S

What is the synonym for Cefadroxil Impurity 10?

The synonym for Cefadroxil Impurity 10 is (6R,7R)-7-((ethoxycarbonyl)amino)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid.

What is the molecular weight of Cefadroxil Impurity 10?

The molecular weight of Cefadroxil Impurity 10 is 286.3.

What is the molecular formula of Cefadroxil Impurity 10?

The molecular formula of Cefadroxil Impurity 10 is C11H14N2O5S.

Is Cefadroxil Impurity 10 a pure substance?

No, Cefadroxil Impurity 10 is an impurity of the antibiotic Cefadroxil.

What is the significance of knowing the molecular weight of Cefadroxil Impurity 10?

The molecular weight helps in the identification and characterization of the impurity.

Is Cefadroxil Impurity 10 commonly found in pharmaceutical products?

Cefadroxil Impurity 10 may be found in small amounts in pharmaceutical products containing Cefadroxil.

How does the molecular formula of Cefadroxil Impurity 10 describe its chemical composition?

The molecular formula C11H14N2O5S indicates the number and types of atoms present in the impurity molecule.

Can the impurity Cefadroxil Impurity 10 affect the effectiveness of Cefadroxil as an antibiotic?

Presence of impurities like Cefadroxil Impurity 10 may affect the purity and potency of Cefadroxil, potentially impacting its effectiveness as an antibiotic.

What methods are typically used to detect and quantify impurities like Cefadroxil Impurity 10 in pharmaceutical products?

Analytical techniques such as HPLC (High-Performance Liquid Chromatography) are commonly used to detect and quantify impurities in pharmaceutical products.

How important is it to monitor and control impurities like Cefadroxil Impurity 10 in pharmaceutical manufacturing?

Monitoring and controlling impurities are crucial in pharmaceutical manufacturing to ensure the quality, safety, and efficacy of the final drug product.

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