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Sitafloxacin Impurity 29

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For Research Use Only | Not For Clinical Use
CATAPB09794
Molecular Weight262.18
Molecular FormulaC11H9F3O4

What is the product name of Sitafloxacin Impurity 29?

The product name of Sitafloxacin Impurity 29 is Sitafloxacin Impurity 29.

What is the molecular weight of Sitafloxacin Impurity 29?

The molecular weight of Sitafloxacin Impurity 29 is 262.18.

What is the molecular formula of Sitafloxacin Impurity 29?

The molecular formula of Sitafloxacin Impurity 29 is C11H9F3O4.

What are the chemical elements present in the molecular formula of Sitafloxacin Impurity 29?

The chemical elements present in the molecular formula of Sitafloxacin Impurity 29 are carbon, hydrogen, fluorine, and oxygen.

What is the significance of Impurity 29 in relation to Sitafloxacin?

Impurity 29 is a specific impurity associated with Sitafloxacin, a fluoroquinolone antibiotic used to treat bacterial infections.

How does the molecular weight of Sitafloxacin Impurity 29 compare to that of Sitafloxacin?

The molecular weight of Sitafloxacin Impurity 29 is 262.18, whereas the molecular weight of Sitafloxacin itself may differ.

Is Sitafloxacin Impurity 29 naturally occurring or synthetic?

Sitafloxacin Impurity 29 is likely a synthetic compound created during the manufacturing process of Sitafloxacin.

Can the presence of Sitafloxacin Impurity 29 affect the effectiveness of Sitafloxacin as an antibiotic?

The presence of impurities in pharmaceutical compounds can impact their efficacy and safety, so the presence of Sitafloxacin Impurity 29 may impact the effectiveness of Sitafloxacin.

Are there specific tests or methods used to detect Sitafloxacin Impurity 29 in pharmaceutical products?

Yes, there are analytical techniques such as chromatography and spectroscopy that can be used to detect and quantify impurities like Sitafloxacin Impurity 29 in pharmaceutical products.

How important is it to monitor and control impurities like Sitafloxacin Impurity 29 in pharmaceutical production?

It is crucial to monitor and control impurities like Sitafloxacin Impurity 29 in pharmaceutical production to ensure the quality, safety, and efficacy of the final products for patient use.

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