Flunarizine Impurity 17

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For Research Use Only | Not For Clinical Use

CAT	APB10496
Molecular Weight	231.3
Molecular Formula	C13H17N3O

What is the molecular weight of Flunarizine Impurity 17?

The molecular weight of Flunarizine Impurity 17 is 231.3.

What is the molecular formula of Flunarizine Impurity 17?

The molecular formula of Flunarizine Impurity 17 is C13H17N3O.

What is the chemical composition of Flunarizine Impurity 17?

The chemical composition of Flunarizine Impurity 17 includes carbon, hydrogen, nitrogen, and oxygen.

Is Flunarizine Impurity 17 a pure substance?

No, Flunarizine Impurity 17 is not a pure substance as it is classified as an impurity.

How is Flunarizine Impurity 17 different from the main active ingredient, Flunarizine?

Flunarizine Impurity 17 is a different chemical compound with its own molecular formula and weight that is distinct from the main active ingredient Flunarizine.

What potential impact can Flunarizine Impurity 17 have on drug quality and efficacy?

Flunarizine Impurity 17 may affect the purity and potency of the drug, potentially impacting its overall quality and efficacy.

Are there regulations regarding the acceptable levels of Flunarizine Impurity 17 in pharmaceutical products?

Yes, regulatory bodies typically set limits on the allowable levels of impurities such as Flunarizine Impurity 17 in pharmaceutical products.

How is Flunarizine Impurity 17 detected and quantified in pharmaceuticals?

Flunarizine Impurity 17 can be detected and quantified through analytical techniques such as chromatography or spectroscopy.

What measures can be taken to minimize the presence of Flunarizine Impurity 17 in pharmaceutical manufacturing?

To minimize the presence of Flunarizine Impurity 17, manufacturers can implement strict quality control measures, optimize synthesis processes, and use high-quality raw materials.

Can Flunarizine Impurity 17 interact with other compounds in pharmaceutical products?

Flunarizine Impurity 17 may potentially interact with other compounds present in pharmaceutical products, which could impact their stability, efficacy, or safety.

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