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Aripiprazole Impurity 17

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For Research Use Only | Not For Clinical Use
CATAPB03092
Synonyms7-((4-bromobutan-2-yl)oxy)-3,4-dihydroquinolin-2(1H)-one
Molecular Weight298.18
Molecular FormulaC13H16BrNO2

What is the molecular weight of Aripiprazole Impurity 17?

The molecular weight of Aripiprazole Impurity 17 is 298.18.

What is an other name for Aripiprazole Impurity 17?

Aripiprazole Impurity 17 is also known as 7-((4-bromobutan-2-yl)oxy)-3,4-dihydroquinolin-2(1H)-one.

What is the molecular formula of Aripiprazole Impurity 17?

The molecular formula of Aripiprazole Impurity 17 is C13H16BrNO2.

Are there any synonyms for Aripiprazole Impurity 17?

Yes, the synonym for Aripiprazole Impurity 17 is 7-((4-bromobutan-2-yl)oxy)-3,4-dihydroquinolin-2(1H)-one.

What elements are present in the molecular formula of Aripiprazole Impurity 17?

The elements present in the molecular formula of Aripiprazole Impurity 17 are carbon, hydrogen, bromine, nitrogen, and oxygen.

What is the chemical structure of Aripiprazole Impurity 17?

The chemical structure of Aripiprazole Impurity 17 is a 3,4-dihydroquinolin-2(1H)-one ring with a bromobutan-2-yl functional group attached.

Can Aripiprazole Impurity 17 be used in pharmaceutical research?

Aripiprazole Impurity 17 is likely a byproduct or impurity in the synthesis of aripiprazole, which is an antipsychotic drug used in the treatment of schizophrenia and bipolar disorder. Its use in pharmaceutical research may vary.

How does the molecular weight of Aripiprazole Impurity 17 compare to that of aripiprazole?

Aripiprazole Impurity 17 has a slightly lower molecular weight compared to aripiprazole, which has a molecular weight of 448.38.

Is Aripiprazole Impurity 17 a commonly encountered impurity in pharmaceutical manufacturing?

Aripiprazole Impurity 17 may be a known impurity in the synthesis of aripiprazole, but its occurrence in pharmaceutical manufacturing may vary depending on the specific procedures and quality control measures in place.

Are there specific methods for identifying and removing Aripiprazole Impurity 17 from pharmaceutical products?

Specific methods for identifying and removing Aripiprazole Impurity 17 from pharmaceutical products would depend on the manufacturing process and the specific impurity profile of the final product. these methods may include analytical techniques such as chromatography or spectroscopy.

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