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Decitabine Impurity 6

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For Research Use Only | Not For Clinical Use
CATAPB04875
Synonyms((2R,3S)-3-acetoxy-5-(4-amino-2-oxo-1,3,5-triazin-1(2H)-yl)tetrahydrofuran-2-yl)methyl acetate
Molecular Weight312.28
Molecular FormulaC12H16N4O6

What is the chemical name for Decitabine Impurity 6?

The chemical name for Decitabine Impurity 6 is ((2R,3S)-3-acetoxy-5-(4-amino-2-oxo-1,3,5-triazin-1(2H)-yl)tetrahydrofuran-2-yl)methyl acetate.

What is the molecular weight of Decitabine Impurity 6?

The molecular weight of Decitabine Impurity 6 is 312.28.

What is the molecular formula of Decitabine Impurity 6?

The molecular formula of Decitabine Impurity 6 is C12H16N4O6.

What are some synonyms for Decitabine Impurity 6?

Some synonyms for Decitabine Impurity 6 include ((2R,3S)-3-acetoxy-5-(4-amino-2-oxo-1,3,5-triazin-1(2H)-yl)tetrahydrofuran-2-yl)methyl acetate.

What is the structure of Decitabine Impurity 6?

Decitabine Impurity 6 has a tetrahydrofuran structure with acetoxy and amino groups attached.

How many nitrogen atoms are present in the molecular formula of Decitabine Impurity 6?

There are four nitrogen atoms present in the molecular formula of Decitabine Impurity 6.

What functional groups are present in Decitabine Impurity 6?

Decitabine Impurity 6 contains acetoxy,- Amino, and triazin functional groups.

What is the significance of Decitabine Impurity 6 in pharmaceutical manufacturing?

Decitabine Impurity 6 is important in pharmaceutical manufacturing as it is a specific impurity that needs to be controlled in the production of the drug Decitabine.

How is Decitabine Impurity 6 typically detected and quantified in pharmaceutical samples?

Decitabine Impurity 6 is typically detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry.

What are some potential implications of the presence of Decitabine Impurity 6 in pharmaceutical products?

The presence of Decitabine Impurity 6 in pharmaceutical products can impact the purity, potency, and safety of the drug, leading to potential quality control issues and regulatory concerns.

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