Fludarabine Impurity 15

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For Research Use Only | Not For Clinical Use

CAT	APB05940
Synonyms	((2R,3R,4S,5S)-5-(6-amino-2-fluoro-9H-purin-9-yl)-3,4-dihydroxy-4-methyltetrahydrofuran-2-yl)methyl dihydrogen phosphate
Molecular Weight	379.24
Molecular Formula	C11H15FN5O7P

What is the molecular weight of Fludarabine Impurity 15?

The molecular weight of Fludarabine Impurity 15 is 379.24.

What is the molecular formula of Fludarabine Impurity 15?

The molecular formula of Fludarabine Impurity 15 is C11H15FN5O7P.

How is Fludarabine Impurity 15 also known as?

Fludarabine Impurity 15 is also known as ((2R,3R,4S,5S)-5-(6-amino-2-fluoro-9H-purin-9-yl)-3,4-dihydroxy-4-methyltetrahydrofuran-2-yl)methyl dihydrogen phosphate.

What is the chemical structure of Fludarabine Impurity 15?

The chemical structure of Fludarabine Impurity 15 contains a dihydrogen phosphate group attached to a purine ring.

What is the significance of the amino and fluoro groups in Fludarabine Impurity 15?

The amino and fluoro groups in Fludarabine Impurity 15 may contribute to its pharmaceutical properties and biological activity.

How many hydrogen atoms are present in the molecular formula of Fludarabine Impurity 15?

Fludarabine Impurity 15 contains a total of 15 hydrogen atoms.

What is the potential role of Fludarabine Impurity 15 in pharmaceutical research?

Fludarabine Impurity 15 may serve as a reference standard or control for the accurate analysis of fludarabine drug formulations.

How does Fludarabine Impurity 15 differ from the main drug, fludarabine?

Fludarabine Impurity 15 is a chemical impurity or related compound of fludarabine, often found in drug samples.

Are there specific methods for detecting and quantifying Fludarabine Impurity 15 in samples?

Yes, analytical techniques such as HPLC or mass spectrometry can be used to detect and quantify Fludarabine Impurity 15.

What potential risks or concerns may arise from the presence of Fludarabine Impurity 15 in pharmaceutical products?

The presence of Fludarabine Impurity 15 in pharmaceutical formulations may impact the efficacy, safety, or stability of the drug product, necessitating quality control measures.

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