Barricetinib impurity B

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For Research Use Only | Not For Clinical Use

CAT	APB06662
Molecular Weight	254.31
Molecular Formula	C10H14N4O2S

What is the molecular weight of Barricetinib impurity B?

The molecular weight of Barricetinib impurity B is 254.31.

What is the molecular formula of Barricetinib impurity B?

The molecular formula of Barricetinib impurity B is C10H14N4O2S.

What is the chemical name of Barricetinib impurity B?

The chemical name of Barricetinib impurity B is Barricetinib impurity B.

What is the structure of Barricetinib impurity B?

The structure of Barricetinib impurity B is composed of carbon, hydrogen, nitrogen, oxygen, and sulfur atoms.

How does Barricetinib impurity B differ from the main compound Barricetinib?

Barricetinib impurity B is a related compound that is impure and not the main active ingredient like Barricetinib.

Is Barricetinib impurity B commonly found in pharmaceutical products?

Barricetinib impurity B is not commonly found in pharmaceutical products as it is considered an impurity.

What are the potential risks or concerns associated with Barricetinib impurity B in pharmaceutical manufacturing?

The presence of Barricetinib impurity B in pharmaceutical products may impact the purity and quality of the final product, leading to potential safety and efficacy concerns.

How is Barricetinib impurity B detected and quantified in pharmaceutical formulations?

Barricetinib impurity B can be detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry.

Are there regulatory limits or guidelines for the acceptable levels of Barricetinib impurity B in pharmaceutical products?

Regulatory agencies may have established limits or guidelines for the acceptable levels of Barricetinib impurity B in pharmaceutical products to ensure safety and quality standards are met.

What steps can be taken to minimize the presence of Barricetinib impurity B in pharmaceutical manufacturing?

Pharmaceutical manufacturers can implement quality control measures, such as rigorous testing and purification processes, to minimize the presence of Barricetinib impurity B in their products.

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