Brivudine Impurity 10

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For Research Use Only | Not For Clinical Use

CAT	APB55520677
CAS	55520-67-7
Structure
Molecular Weight	254.24
Molecular Formula	C11H14N2O5

What is the name of the product with CAS number 55520-67-7?

The product is Brivudine Impurity 10.

What is the molecular weight of Brivudine Impurity 10?

The molecular weight is 254.24.

What is the molecular formula of Brivudine Impurity 10?

The molecular formula is C11H14N2O5.

What is the chemical structure of Brivudine Impurity 10 based on its molecular formula?

The chemical structure of Brivudine Impurity 10 is composed of 11 carbon atoms, 14 hydrogen atoms, 2 nitrogen atoms, and 5 oxygen atoms.

What is the significance of the presence of Impurity 10 in Brivudine?

The presence of Impurity 10 in Brivudine indicates potential impurities or by-products in the manufacturing process that may affect the purity and quality of the final product.

How can the purity of Brivudine be affected by the presence of Impurity 10?

The presence of Impurity 10 can lower the purity of Brivudine, leading to potential safety and efficacy concerns in its use.

What are the potential implications of Impurity 10 in the production of Brivudine?

Impurity 10 can impact the stability, pharmacological properties, and overall effectiveness of Brivudine if not properly controlled during manufacturing.

How can the presence of Impurity 10 be monitored and controlled in the production of Brivudine?

Methods such as quality control testing, process optimization, and purification techniques can be employed to monitor and control the levels of Impurity 10 in the production of Brivudine.

Are there regulations or guidelines regarding the allowable levels of Impurity 10 in Brivudine products?

Regulatory authorities may have established limits or guidelines for the acceptable levels of Impurity 10 in Brivudine products to ensure safety and quality standards are met.

What steps can be taken to minimize the presence of Impurity 10 in Brivudine formulations?

Manufacturers can implement stringent quality control measures, conduct thorough process validation, and continuously monitor and optimize production processes to minimize the presence of Impurity 10 in Brivudine formulations.

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