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Fludarabine EP impurity K

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For Research Use Only | Not For Clinical Use
CATAPB05941
Synonyms((2R,3S,4S,5R)-5-(6-amino-2-chloro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl dihydrogen phosphate
Molecular Weight381.67
Molecular FormulaC10H13ClN5O7P

What is the molecular weight of Fludarabine EP impurity K?

The molecular weight is 381.67 g/mol.

What is the molecular formula of Fludarabine EP impurity K?

The molecular formula is C10H13ClN5O7P.

What is the chemical structure of Fludarabine EP impurity K?

The chemical structure consists of a tetrahydrofuran ring attached to a purine base with a phosphate group.

What is the role of Fludarabine EP impurity K in pharmaceuticals?

The role of Fludarabine EP impurity K may be to act as an impurity in the pharmaceutical product, potentially affecting its purity and efficacy.

How does Fludarabine EP impurity K differ from the main compound, Fludarabine EP?

Fludarabine EP impurity K likely differs from the main compound in terms of structure and properties due to the presence of impurities.

How is Fludarabine EP impurity K detected and quantified in pharmaceutical products?

Fludarabine EP impurity K may be detected and quantified using analytical techniques such as chromatography and spectroscopy.

What precautions should be taken to minimize the presence of Fludarabine EP impurity K in pharmaceutical products?

Precautions such as proper handling, storage, and manufacturing processes should be implemented to minimize impurities like Fludarabine EP impurity K.

Can Fludarabine EP impurity K potentially impact the safety or efficacy of a pharmaceutical product?

Yes, Fludarabine EP impurity K can potentially impact the safety and efficacy of a pharmaceutical product if present in significant amounts, as impurities can affect the quality and stability of the product.

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