Tofacitinib Impurity F

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For Research Use Only | Not For Clinical Use

CAT	APB477600741
CAS	477600-74-1
Structure
Synonyms	N-methyl-N-((3R,4R)-4-methylpiperidin-3-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine
Molecular Weight	245.32
Molecular Formula	C13H19N5

What is the product name of CAS 477600-74-1?

The product name is Tofacitinib Impurity F.

What are the synonyms for Tofacitinib Impurity F?

One of the synonyms is N-methyl-N-((3R,4R)-4-methylpiperidin-3-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine.

What is the molecular weight of Tofacitinib Impurity F?

The molecular weight is 245.32.

What is the molecular formula of Tofacitinib Impurity F?

The molecular formula is C13H19N5.

What is the chemical structure of Tofacitinib Impurity F?

The chemical structure is represented by N-methyl-N-((3R,4R)-4-methylpiperidin-3-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine.

What is the role of Tofacitinib Impurity F in pharmaceuticals?

Tofacitinib Impurity F is a related compound or impurity that may be present in Tofacitinib or related pharmaceutical products.

How can Tofacitinib Impurity F affect the quality of pharmaceutical products?

The presence of impurities like Tofacitinib Impurity F can affect the purity, stability, and efficacy of pharmaceutical products.

What methods can be used to detect Tofacitinib Impurity F in pharmaceutical formulations?

Analytical techniques like HPLC (High-Performance Liquid Chromatography) can be used to detect and quantify impurities like Tofacitinib Impurity F in pharmaceutical formulations.

Are there any regulations or guidelines regarding the permissible levels of Tofacitinib Impurity F in pharmaceutical products?

Regulatory authorities may establish allowable limits for impurities like Tofacitinib Impurity F in pharmaceutical products to ensure safety and quality standards are met.

How can manufacturers ensure the control of Tofacitinib Impurity F in their pharmaceutical products?

Manufacturers can implement stringent quality control measures, such as using high-quality starting materials and rigorous purification processes, to minimize the presence of Tofacitinib Impurity F in their pharmaceutical products.

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