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Decitabine Impurity 12

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For Research Use Only | Not For Clinical Use
CATAPB04871
Synonyms((2R,3S,5S)-5-(4-amino-2-oxo-1,3,5-triazin-1(2H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl acetate
Molecular Weight270.24
Molecular FormulaC10H14N4O5

What is the molecular weight of Decitabine Impurity 12?

The molecular weight of Decitabine Impurity 12 is 270.24.

What is the molecular formula of Decitabine Impurity 12?

The molecular formula of Decitabine Impurity 12 is C10H14N4O5.

How is Decitabine Impurity 12 also known?

Decitabine Impurity 12 is also known as ((2R,3S,5S)-5-(4-amino-2-oxo-1,3,5-triazin-1(2H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl acetate.

What is the structure of Decitabine Impurity 12?

The structure of Decitabine Impurity 12 is a tetrahydrofuran ring with an amino triazine group attached.

What is the chemical composition of Decitabine Impurity 12?

The chemical composition of Decitabine Impurity 12 includes carbon, hydrogen, nitrogen, and oxygen atoms.

What is the importance of knowing the molecular weight of Decitabine Impurity 12?

Knowing the molecular weight of Decitabine Impurity 12 is essential for determining its chemical properties and for quality control purposes.

How can the molecular formula of Decitabine Impurity 12 be represented in a structural diagram?

The molecular formula C10H14N4O5 of Decitabine Impurity 12 can be represented in a structural diagram showing the arrangement of atoms and bonds.

What are the potential impurities in Decitabine Impurity 12?

Potential impurities in Decitabine Impurity 12 include related compounds with similar molecular structures.

How is Decitabine Impurity 12 synthesized in the laboratory?

Decitabine Impurity 12 can be synthesized in the laboratory by specific chemical reactions involving the combination of different starting materials.

What is the significance of Decitabine Impurity 12 in pharmaceutical research and development?

Decitabine Impurity 12 is important in pharmaceutical research and development as it can help identify, characterize, and quantify impurities in drug substances, affecting the quality and safety of the final product.

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