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Nebivolol Impurity 14

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For Research Use Only | Not For Clinical Use
CATAPB08798
Molecular Weight230.66
Molecular FormulaC11H12ClFO2

What is the molecular weight of Nebivolol Impurity 14?

The molecular weight of Nebivolol Impurity 14 is 230.66.

What is the molecular formula of Nebivolol Impurity 14?

The molecular formula of Nebivolol Impurity 14 is C11H12ClFO2.

What is the chemical structure of Nebivolol Impurity 14?

The chemical structure of Nebivolol Impurity 14 is made up of 11 carbon atoms, 12 hydrogen atoms, 1 chlorine atom, 1 fluorine atom, and 2 oxygen atoms.

How is Nebivolol Impurity 14 used in pharmaceutical research?

Nebivolol Impurity 14 is used in pharmaceutical research as a standard reference material for testing and validating analytical methods for detecting impurities in Nebivolol formulations.

What role does Nebivolol Impurity 14 play in the quality control of Nebivolol products?

Nebivolol Impurity 14 serves as a benchmark for assessing the purity and quality of Nebivolol products by providing a standard for comparison in analytical testing.

What are some potential impurities that could be present in Nebivolol products?

Some potential impurities that could be present in Nebivolol products include related substances from the manufacturing process, degradation products, and impurities from raw materials.

How is Nebivolol Impurity 14 synthesized in the laboratory?

Nebivolol Impurity 14 can be synthesized in the laboratory through specific chemical reactions involving precursors with known properties and reactivity.

What analytical techniques are commonly used to detect Nebivolol Impurity 14 in pharmaceutical samples?

High-performance liquid chromatography (HPLC) and mass spectrometry (MS) are commonly used analytical techniques to detect Nebivolol Impurity 14 in pharmaceutical samples.

How can the presence of Nebivolol Impurity 14 impact the safety and efficacy of Nebivolol products?

The presence of Nebivolol Impurity 14 can potentially compromise the safety and efficacy of Nebivolol products by introducing unknown impurities that may have adverse effects on patients or reduce the potency of the active pharmaceutical ingredient.

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