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Cangrelor Impurity 22

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For Research Use Only | Not For Clinical Use
CATAPB11947
Molecular Weight395.38
Molecular FormulaC11H12F3N7O2S2

What is the molecular weight of Cangrelor Impurity 22?

The molecular weight of Cangrelor Impurity 22 is 395.38.

What is the molecular formula of Cangrelor Impurity 22?

The molecular formula of Cangrelor Impurity 22 is C11H12F3N7O2S2.

What is the chemical structure of Cangrelor Impurity 22?

The chemical structure of Cangrelor Impurity 22 is C11H12F3N7O2S2.

What type of impurity is Cangrelor Impurity 22?

Cangrelor Impurity 22 is an impurity related to the medication Cangrelor.

What are the specific atoms present in the molecular formula of Cangrelor Impurity 22?

The molecular formula of Cangrelor Impurity 22 contains atoms of carbon, hydrogen, fluorine, nitrogen, oxygen, and sulfur.

What is the importance of identifying and characterizing Cangrelor Impurity 22?

Identifying and characterizing Cangrelor Impurity 22 is important for determining the purity and quality of the Cangrelor medication.

How is Cangrelor Impurity 22 detected and quantified in pharmaceutical samples?

Cangrelor Impurity 22 can be detected and quantified in pharmaceutical samples using analytical techniques such as HPLC (High Performance Liquid Chromatography).

What is the significance of the molecular weight of Cangrelor Impurity 22 in pharmaceutical analysis?

The molecular weight of Cangrelor Impurity 22 is significant in pharmaceutical analysis as it helps in determining the purity and concentration of the impurity in a sample.

How does the molecular formula of Cangrelor Impurity 22 affect its chemical properties?

The molecular formula of Cangrelor Impurity 22 determines its chemical composition and behavior, influencing its interactions with other compounds and its stability.

Why is it essential to monitor and control the levels of Cangrelor Impurity 22 in pharmaceutical products?

Monitoring and controlling the levels of Cangrelor Impurity 22 in pharmaceutical products is essential to ensure the safety and efficacy of the medication, as impurities can affect the quality and performance of the product.

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