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Empagliflozin Impurity 129

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For Research Use Only | Not For Clinical Use
CATAPB05685
Synonyms(2-chloro-3-iodophenyl)(4-fluorophenyl)methanone
Molecular Weight359.92
Molecular FormulaC13H7ClFIO

What is the molecular weight of Empagliflozin Impurity 129?

The molecular weight of Empagliflozin Impurity 129 is 359.92.

What is the molecular formula of Empagliflozin Impurity 129?

The molecular formula of Empagliflozin Impurity 129 is C13H7ClFIO.

What are some synonyms for Empagliflozin Impurity 129?

One synonym for Empagliflozin Impurity 129 is (2-chloro-3-iodophenyl)(4-fluorophenyl)methanone.

What is the chemical structure of Empagliflozin Impurity 129?

The chemical structure of Empagliflozin Impurity 129 is C13H7ClFIO.

What are the elements present in the molecular formula of Empagliflozin Impurity 129?

The elements present in the molecular formula of Empagliflozin Impurity 129 are carbon (C), hydrogen (H), chlorine (Cl), fluorine (F), and iodine (I).

How many carbon atoms are there in Empagliflozin Impurity 129?

There are 13 carbon atoms in Empagliflozin Impurity 129.

What is the significance of Empagliflozin Impurity 129 in pharmaceutical research?

Empagliflozin Impurity 129 is an impurity that can affect the effectiveness and safety of the drug Empagliflozin, and it is important to identify and monitor its presence during production.

How is Empagliflozin Impurity 129 detected and quantified in pharmaceutical products?

Empagliflozin Impurity 129 can be detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry.

Why is it important to control the levels of Empagliflozin Impurity 129 in pharmaceutical products?

Controlling the levels of Empagliflozin Impurity 129 is important to ensure the quality, safety, and efficacy of the drug product for patient use.

How can the presence of Empagliflozin Impurity 129 impact the quality of pharmaceutical products?

The presence of Empagliflozin Impurity 129 can lead to decreased potency, increased toxicity, or unwanted side effects in pharmaceutical products, affecting their overall quality and safety.

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