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Isavuconazole Impurity 8

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For Research Use Only | Not For Clinical Use
CATAPB10587
Molecular Weight312.34
Molecular FormulaC13H14F2N4OS

What is the molecular weight of Isavuconazole Impurity 8?

The molecular weight of Isavuconazole Impurity 8 is 312.34.

What is the molecular formula of Isavuconazole Impurity 8?

The molecular formula of Isavuconazole Impurity 8 is C13H14F2N4OS.

What is the specific name of this chemical compound?

The specific name of this chemical compound is Isavuconazole Impurity 8.

What are the main elements present in the molecular formula of Isavuconazole Impurity 8?

The main elements present in the molecular formula of Isavuconazole Impurity 8 are carbon (C), hydrogen (H), fluorine (F), nitrogen (N), and sulfur (S).

What is the significance of Isavuconazole Impurity 8?

Isavuconazole Impurity 8 is an impurity found in the chemical structure of Isavuconazole, a drug used in the treatment of various fungal infections.

How is Isavuconazole Impurity 8 formed?

Isavuconazole Impurity 8 is formed as a byproduct or impurity during the synthesis or production of Isavuconazole.

What is the role of Isavuconazole Impurity 8 in pharmaceutical manufacturing?

Isavuconazole Impurity 8 is important in pharmaceutical manufacturing as it needs to be identified and controlled to ensure the quality and safety of the final drug product.

How is Isavuconazole Impurity 8 detected and analyzed?

Isavuconazole Impurity 8 is detected and analyzed using various analytical techniques such as chromatography, mass spectrometry, and spectroscopy.

What are the possible implications of having Isavuconazole Impurity 8 in a pharmaceutical product?

Having Isavuconazole Impurity 8 in a pharmaceutical product may affect the efficacy, safety, or stability of the drug, and therefore must be monitored and controlled.

How is the presence of Isavuconazole Impurity 8 regulated in pharmaceuticals?

The presence of Isavuconazole Impurity 8 in pharmaceuticals is regulated by health authorities and pharmacopoeias, which set limits and guidelines for impurity levels in drug products.

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