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Abacavir Impurity 16

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For Research Use Only | Not For Clinical Use
CATAPB141271127
CAS141271-12-7
Synonyms((1S,4R)-4-((2,5-diamino-6-chloropyrimidin-4-yl)amino)cyclopent-2-en-1-yl)methanol
Molecular Weight255.70
Molecular FormulaC10H14ClN5O

What is the product name of CAS 141271-12-7?

The product name is Abacavir Impurity 16.

What is the synonym for Abacavir Impurity 16?

The synonym the ((1S,4R)-4-((2,5-diamino-6-chloropyrimidin-4-yl)amino)cyclopent-2-en-1-yl)methanol.

What is the molecular weight of Abacavir Impurity 16?

The molecular weight is 255.70.

What is the molecular formula of Abacavir Impurity 16?

The molecular formula is C10H14ClN5O.

What is the chemical structure of Abacavir Impurity 16?

The chemical structure is ((1S,4R)-4-((2,5-diamino-6-chloropyrimidin-4-yl)amino)cyclopent-2-en-1-yl)methanol.

What is the significance of impurity 16 in relation to Abacavir?

Impurity 16 is a specific impurity related to the drug Abacavir, which may affect the quality or safety of the medication.

How can Abacavir Impurity 16 be detected in pharmaceuticals?

Abacavir Impurity 16 can be detected through various analytical techniques such as chromatography or spectroscopy.

What potential effects can Abacavir Impurity 16 have on the efficacy of Abacavir?

Abacavir Impurity 16 may impact the purity and effectiveness of Abacavir, leading to potential health risks for patients.

How can manufacturers ensure the absence of Abacavir Impurity 16 in their products?

Manufacturers can perform strict quality control measures and testing protocols to ensure the absence of Abacavir Impurity 16 in their final pharmaceutical products.

Are there regulations or guidelines in place regarding the presence of impurities like Abacavir Impurity 16 in pharmaceutical products?

Yes, regulatory bodies like the FDA or EMA have set limits and guidelines for impurities in pharmaceutical products, including Abacavir Impurity 16, to ensure patient safety and product quality.

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