Fludarabine EP impurity I

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For Research Use Only | Not For Clinical Use

CAT	APB7561548
CAS	7561-54-8
Synonyms	((2R,3S,4S,5R)-5-(2,6-diamino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl dihydrogen phosphate
Molecular Weight	362.24
Molecular Formula	C10H15N6O7P

What is the name and CAS number of the product?

The name of the product is Fludarabine EP impurity I and its CAS number is 7561-54-8.

Can you provide the molecular weight and formula of Fludarabine EP impurity I?

The molecular weight of Fludarabine EP impurity I is 362.24 and its molecular formula is C10H15N6O7P.

What is the synonym of Fludarabine EP impurity I?

The synonym of Fludarabine EP impurity I is ((2R,3S,4S,5R)-5-(2,6-diamino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl dihydrogen phosphate.

Can you describe the chemical structure of Fludarabine EP impurity I?

The chemical structure of Fludarabine EP impurity I is a tetrahydrofuran ring connected to a purine base with a phosphate group.

What is the significance of Fludarabine EP impurity I in pharmaceutical research?

Fludarabine EP impurity I is important in pharmaceutical research as it is a known impurity in the drug Fludarabine, and understanding its properties and characteristics can help in quality control and optimization of the drug.

How is Fludarabine EP impurity I synthesized?

Fludarabine EP impurity I can be synthesized through specific chemical reactions involving the transformation of certain precursors into the final compound.

What are the potential applications of Fludarabine EP impurity I in pharmaceutical development?

Fludarabine EP impurity I can be used as a reference standard in analytical methods for the identification and quantification of impurities in Fludarabine drug substances.

How does Fludarabine EP impurity I impact the pharmacological profile of the drug?

Fludarabine EP impurity I, as an impurity in Fludarabine, may affect the purity, stability, and efficacy of the drug, hence monitoring and controlling its levels is important in pharmaceutical manufacturing.

Are there any known side effects or risks associated with Fludarabine EP impurity I?

The specific side effects or risks associated with Fludarabine EP impurity I may depend on its concentration and presence in the drug product, and further studies may be needed to fully understand its implications.

How can researchers ensure the quality and purity of Fludarabine EP impurity I for use in pharmaceutical studies?

Researchers can ensure the quality and purity of Fludarabine EP impurity I by using standardized analytical methods, conducting thorough characterization tests, and following good manufacturing practices in its synthesis and handling.

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