Etravirine Impurity 21

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For Research Use Only | Not For Clinical Use

CAT	APB12015
Molecular Weight	353.56
Molecular Formula	C11H6BrClN6O

What is the molecular weight of Etravirine Impurity 21?

The molecular weight of Etravirine Impurity 21 is 353.56.

What is the molecular formula of Etravirine Impurity 21?

The molecular formula of Etravirine Impurity 21 is C11H6BrClN6O.

What is the significance of identifying Etravirine Impurity 21?

Identifying Etravirine Impurity 21 is important for pharmaceutical quality control and research purposes.

How can Etravirine Impurity 21 impact the efficacy of a medication?

Etravirine Impurity 21 can potentially affect the efficacy and safety of a medication containing it as an impurity.

What methods are used to detect Etravirine Impurity 21 in pharmaceutical products?

Various analytical techniques such as HPLC, LC-MS, and NMR spectroscopy can be used to detect Etravirine Impurity 21 in pharmaceutical products.

Why is it essential to monitor the levels of Etravirine Impurity 21 during pharmaceutical manufacturing?

Monitoring the levels of Etravirine Impurity 21 ensures that the final product meets quality standards and regulatory requirements.

What are some potential sources of Etravirine Impurity 21 in pharmaceutical manufacturing?

Etravirine Impurity 21 can be introduced during synthesis, storage, or handling of raw materials in pharmaceutical manufacturing processes.

Can Etravirine Impurity 21 impact the stability of a pharmaceutical product?

Yes, Etravirine Impurity 21 can affect the stability of a pharmaceutical product, leading to potential degradation or altered efficacy over time.

How can the presence of Etravirine Impurity 21 be minimized in pharmaceutical products?

Implementing strict quality control measures, proper storage conditions, and using high-quality raw materials can help minimize the presence of Etravirine Impurity 21 in pharmaceutical products.

What are the potential risks associated with the presence of Etravirine Impurity 21 in medications?

The presence of Etravirine Impurity 21 in medications can pose risks such as reduced efficacy, unexpected side effects, and non-compliance with regulatory standards.

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