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Alvimopan impurity B

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For Research Use Only | Not For Clinical Use
CATAPB02528
Synonyms3-((3S,4S)-3,4-dimethylpiperidin-4-yl)phenol
Molecular Weight205.3
Molecular FormulaC13H19NO

What is the synonym for Alvimopan impurity B?

The synonym for Alvimopan impurity B is 3-((3S,4S)-3,4-dimethylpiperidin-4-yl)phenol.

What is the molecular weight of Alvimopan impurity B?

The molecular weight of Alvimopan impurity B is 205.3.

What is the molecular formula of Alvimopan impurity B?

The molecular formula of Alvimopan impurity B is C13H19NO.

What is the chemical structure of Alvimopan impurity B?

The chemical structure of Alvimopan impurity B contains a piperidine ring with a phenol group attached.

How is Alvimopan impurity B related to the drug Alvimopan?

Alvimopan impurity B is a related compound or impurity that may be present in the drug Alvimopan.

What is the significance of identifying and monitoring impurities like Alvimopan impurity B in pharmaceuticals?

Identifying and monitoring impurities like Alvimopan impurity B is important for ensuring the safety and efficacy of pharmaceutical products.

How is Alvimopan impurity B typically detected and quantified in pharmaceutical samples?

Alvimopan impurity B is typically detected and quantified using analytical techniques such as HPLC or LC-MS.

Why is it important to control the levels of impurities like Alvimopan impurity B in pharmaceutical products?

Controlling the levels of impurities like Alvimopan impurity B is crucial for meeting regulatory requirements and ensuring product quality.

What potential risks or adverse effects could be associated with the presence of Alvimopan impurity B in pharmaceuticals?

The presence of impurities like Alvimopan impurity B could potentially impact the stability, safety, and efficacy of pharmaceutical products.

What measures can be taken to reduce or eliminate impurities like Alvimopan impurity B in pharmaceutical manufacturing processes?

Measures to reduce or eliminate impurities like Alvimopan impurity B may include adjusting manufacturing processes, using higher purity starting materials, and implementing strict quality control measures.

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