Iloperidone impurity 27

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For Research Use Only | Not For Clinical Use

CAT	APB11910
Molecular Weight	242.7
Molecular Formula	C12H15ClO3

What is the molecular weight of Iloperidone impurity 27?

The molecular weight of Iloperidone impurity 27 is 242.7.

What is the molecular formula of Iloperidone impurity 27?

The molecular formula of Iloperidone impurity 27 is C12H15ClO3.

What is the chemical structure of Iloperidone impurity 27?

The chemical structure of Iloperidone impurity 27 has 12 carbon atoms, 15 hydrogen atoms, one chlorine atom, and three oxygen atoms arranged in a specific configuration.

How is Iloperidone impurity 27 classified in terms of its molecular composition?

Iloperidone impurity 27 is classified as a compound composed of carbon, hydrogen, chlorine, and oxygen atoms.

Why is it important to identify impurities like Iloperidone impurity 27 in pharmaceutical products?

Identifying impurities like Iloperidone impurity 27 is important for ensuring the quality, safety, and efficacy of pharmaceutical products.

Are there specific regulations or guidelines concerning the presence of Iloperidone impurity 27 in pharmaceutical products?

Yes, regulatory bodies often set limits on the amount of impurities like Iloperidone impurity 27 that are allowed in pharmaceutical products.

How is Iloperidone impurity 27 typically detected and quantified in pharmaceutical samples?

Iloperidone impurity 27 is typically detected and quantified using analytical techniques such as chromatography or spectroscopy.

What are the potential health risks associated with the presence of Iloperidone impurity 27 in pharmaceutical products?

The presence of impurities like Iloperidone impurity 27 could potentially pose health risks to patients, depending on the nature and concentration of the impurity.

How can pharmaceutical manufacturers ensure that the levels of Iloperidone impurity 27 remain below regulatory limits?

Pharmaceutical manufacturers can implement strict quality control measures throughout the production process to monitor and minimize the presence of impurities like Iloperidone impurity 27.

What steps can be taken to remove or reduce the levels of Iloperidone impurity 27 in pharmaceutical products?

Purification techniques, such as recrystallization or column chromatography, can be employed to remove or reduce the levels of impurities like Iloperidone impurity 27 in pharmaceutical products.

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