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Levocabastine Impurity 10

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For Research Use Only | Not For Clinical Use
CATAPB179064610
CAS179064-61-0
Structure
Molecular Weight217.24
Molecular FormulaC13H12FNO

What is the molecular weight of Levocabastine Impurity 10?

The molecular weight of Levocabastine Impurity 10 is 217.24.

What is the molecular formula of Levocabastine Impurity 10?

The molecular formula of Levocabastine Impurity 10 is C13H12FNO.

What is the CAS number of Levocabastine Impurity 10?

The CAS number of Levocabastine Impurity 10 is 179064-61-0.

What is the chemical structure of Levocabastine Impurity 10?

The chemical structure of Levocabastine Impurity 10 includes 13 carbon atoms, 12 hydrogen atoms, 1 fluorine atom, and 1 nitrogen atom.

Is Levocabastine Impurity 10 used as an active pharmaceutical ingredient?

Levocabastine Impurity 10 is not typically used as an active pharmaceutical ingredient, but ra- Ther as an impurity in pharmaceutical products.

What is the significance of identifying impurities in pharmaceutical products?

Identifying impurities in pharmaceutical products is crucial for ensuring the safety and efficacy of the final drug product.

How is Levocabastine Impurity 10 typically detected and quantified in pharmaceutical samples?

Levocabastine Impurity 10 is typically detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC).

What potential effects can impurities like Levocabastine Impurity 10 have on pharmaceutical products?

Impurities like Levocabastine Impurity 10 can affect the stability, shelf life, and overall quality of pharmaceutical products.

Are there specific regulatory guidelines for allowable levels of impurities in pharmaceutical products?

Yes, regulatory agencies such as the FDA and EMA have guidelines for allowable levels of impurities in pharmaceutical products.

How can manufacturers control and reduce the presence of impurities like Levocabastine Impurity 10 in pharmaceutical products?

Manufacturers can control and reduce impurities by implementing strict quality control measures, utilizing proper storage and handling procedures, and conducting thorough testing throughout the production process.

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