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Levosimendan Impurity 14

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For Research Use Only | Not For Clinical Use
CATAPB36725414
CAS36725-41-4
Molecular Weight222.67
Molecular FormulaC11H11ClN2O

What is the molecular weight of Levosimendan Impurity 14?

The molecular weight of Levosimendan Impurity 14 is 222.67.

What is the molecular formula of Levosimendan Impurity 14?

The molecular formula of Levosimendan Impurity 14 is C11H11ClN2O.

What is the CAS number of Levosimendan Impurity 14?

The CAS number of Levosimendan Impurity 14 is 36725-41-4.

What are the elements present in the molecular formula of Levosimendan Impurity 14?

The elements present in the molecular formula of Levosimendan Impurity 14 are carbon, hydrogen, chlorine, nitrogen, and oxygen.

How many carbon atoms are there in the molecular formula of Levosimendan Impurity 14?

There are 11 carbon atoms in the molecular formula of Levosimendan Impurity 14.

How many hydrogen atoms are there in the molecular formula of Levosimendan Impurity 14?

There are 11 hydrogen atoms in the molecular formula of Levosimendan Impurity 14.

What is the significance of Levosimendan Impurity 14 in pharmaceutical research?

Levosimendan Impurity 14 is important in pharmaceutical research as it is an impurity that needs to be identified and characterized in the synthesis of the drug Levosimendan.

How is Levosimendan Impurity 14 typically synthesized?

Levosimendan Impurity 14 is typically synthesized as part of the production process of Levosimendan, a drug used for the treatment of heart failure.

What is the structural difference between Levosimendan and Levosimendan Impurity 14?

The structural difference between Levosimendan and Levosimendan Impurity 14 lies in the presence of impurities or additional atoms/groups in the molecular structure of the impurity.

How important is the detection and quantification of Levosimendan Impurity 14 in pharmaceutical manufacturing?

The detection and quantification of Levosimendan Impurity 14 are crucial in pharmaceutical manufacturing to ensure the safety, efficacy, and quality of the final drug product.

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