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Cefoperazone Impurity O

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For Research Use Only | Not For Clinical Use
CATAPB06975
Molecular Weight346.38
Molecular FormulaC10H14N6O4S2

What is the molecular weight of Cefoperazone Impurity O?

The molecular weight of Cefoperazone Impurity O is 346.38.

What is the molecular formula of Cefoperazone Impurity O?

The molecular formula of Cefoperazone Impurity O is C10H14N6O4S2.

What is the structure of Cefoperazone Impurity O based on its molecular formula?

The structure of Cefoperazone Impurity O includes carbon, hydrogen, nitrogen, oxygen, and sulfur atoms.

How many carbon atoms are present in the molecular formula of Cefoperazone Impurity O?

There are 10 carbon atoms present in the molecular formula of Cefoperazone Impurity O.

What are the elements present in the molecular formula of Cefoperazone Impurity O?

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

How many hydrogen atoms are present in the molecular formula of Cefoperazone Impurity O?

There are 14 hydrogen atoms present in the molecular formula of Cefoperazone Impurity O.

What is the significance of identifying impurities in pharmaceutical products like Cefoperazone Impurity O?

Identifying impurities is crucial in ensuring the safety and efficacy of pharmaceutical products like Cefoperazone Impurity O.

How is Cefoperazone Impurity O typically synthesized in a laboratory setting?

Cefoperazone Impurity O can be synthesized through specific chemical reactions involving the elements present in its molecular formula.

What analytical techniques can be used to detect and quantify Cefoperazone Impurity O in pharmaceutical formulations?

High-performance liquid chromatography (HPLC) and mass spectrometry are commonly used analytical techniques for detecting and quantifying Cefoperazone Impurity O.

Why is it important for pharmaceutical companies to monitor and control impurities in products like Cefoperazone Impurity O?

Controlling impurities ensures the quality, safety, and effectiveness of pharmaceutical products, maintaining regulatory compliance and patient well-being.

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