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Istradefylline Impurity 2

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For Research Use Only | Not For Clinical Use
CATAPB08281
Molecular Weight254.29
Molecular FormulaC11H18N4O3

What is the molecular weight of Istradefylline Impurity 2?

The molecular weight of Istradefylline Impurity 2 is 254.29.

What is the molecular formula of Istradefylline Impurity 2?

The molecular formula of Istradefylline Impurity 2 is C11H18N4O3.

How is Istradefylline Impurity 2 categorized based on its molecular structure?

Istradefylline Impurity 2 is categorized based on its molecular structure as C11H18N4O3.

What are the individual elements present in the molecular formula of Istradefylline Impurity 2?

The individual elements present in the molecular formula of Istradefylline Impurity 2 are carbon, hydrogen, nitrogen, and oxygen.

What is the chemical composition of Istradefylline Impurity 2?

The chemical composition of Istradefylline Impurity 2 includes 11 carbon atoms, 18 hydrogen atoms, 4 nitrogen atoms, and 3 oxygen atoms.

What is the significance of Istradefylline Impurity 2 in pharmaceutical research?

Istradefylline Impurity 2 is significant in pharmaceutical research as it is an impurity that may impact the efficacy or safety of the drug Istradefylline.

How does the molecular weight of Istradefylline Impurity 2 compare to other related compounds?

The molecular weight of Istradefylline Impurity 2 is specific to its structure and distinguishes it from other related compounds.

What potential effects can Istradefylline Impurity 2 have on drug formulations?

Istradefylline Impurity 2 may affect the stability, bioavailability, or pharmacological properties of drug formulations containing it.

How is the presence of Istradefylline Impurity 2 detected in pharmaceutical products?

The presence of Istradefylline Impurity 2 can be detected through analytical techniques such as chromatography or mass spectrometry.

What considerations should be taken into account when dealing with Istradefylline Impurity 2 in drug development?

When dealing with Istradefylline Impurity 2 in drug development, factors such as impurity levels, potential interactions, and regulatory guidelines should be carefully considered to ensure product quality and safety.

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