Quetiapine impurity 30

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For Research Use Only | Not For Clinical Use

CAT	APB14258436
CAS	14258-43-6
Molecular Weight	262.35
Molecular Formula	C12H26N2O4

What is the product name of CAS 14258-43-6?

The product name is Quetiapine impurity 30.

What is the molecular weight of Quetiapine impurity 30?

The molecular weight is 262.35.

What is the molecular formula of Quetiapine impurity 30?

The molecular formula is C12H26N2O4.

What is the chemical structure of Quetiapine impurity 30 based on its molecular formula?

The chemical structure of Quetiapine impurity 30 is composed of 12 carbon atoms, 26 hydrogen atoms, 2 nitrogen atoms, and 4 oxygen atoms.

What is the significance of Quetiapine impurity 30 in pharmaceutical research?

It is important in pharmaceutical research as it is an impurity that needs to be identified and characterized in the manufacturing process of the drug Quetiapine.

How is Quetiapine impurity 30 produced?

Quetiapine impurity 30 is produced as a byproduct or contaminant during the synthesis of Quetiapine.

Is Quetiapine impurity 30 harmful to human health?

The impact of Quetiapine impurity 30 on human health depends on its concentration and potential toxicity, which should be evaluated through thorough analysis.

How can Quetiapine impurity 30 be detected and quantified in pharmaceutical samples?

Quetiapine impurity 30 can be detected and quantified using analytical techniques such as HPLC (High-Performance Liquid Chromatography) and MS (Mass Spectrometry).

Are there regulations or guidelines regarding the acceptable levels of Quetiapine impurity 30 in pharmaceutical products?

Regulatory bodies such as the FDA and EMA provide guidelines on the acceptable levels of impurities in pharmaceutical products, including Quetiapine impurity 30.

What are the potential risks of Quetiapine impurity 30 if not properly monitored in pharmaceutical production?

If not properly monitored, Quetiapine impurity 30 could potentially impact the quality, safety, and efficacy of the final drug product, leading to adverse effects on patients.

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