Xanomeline Impurity 4

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For Research Use Only | Not For Clinical Use

CAT	APB11425
Molecular Weight	273.34
Molecular Formula	C11H11D4N3O3S

What is the molecular weight of Xanomeline Impurity 4?

The molecular weight of Xanomeline Impurity 4 is 273.34.

What is the molecular formula of Xanomeline Impurity 4?

The molecular formula of Xanomeline Impurity 4 is C11H11D4N3O3S.

What is the chemical structure of Xanomeline Impurity 4 based on its molecular formula?

The chemical structure of Xanomeline Impurity 4 contains 11 carbon atoms, 11 deuterium atoms, 3 nitrogen atoms, 3 oxygen atoms, and 1 sulfur atom.

How many deuterium atoms are present in the molecular formula of Xanomeline Impurity 4?

There are 11 deuterium atoms present in the molecular formula of Xanomeline Impurity 4.

Is Xanomeline Impurity 4 an organic compound?

Yes, Xanomeline Impurity 4 is an organic compound.

What are the possible functional groups present in Xanomeline Impurity 4?

The possible functional groups present in Xanomeline Impurity 4 include amine, sulfonamide, and possibly- Others.

What is the significance of impurity 4 in the context of Xanomeline?

Impurity 4 is a specific impurity that is associated with the synthesis or production of Xanomeline, and its presence may affect the purity or efficacy of the final product.

How can Xanomeline Impurity 4 be detected and quantified in a sample?

Xanomeline Impurity 4 can be detected and quantified using analytical techniques such as HPLC (High Performance Liquid Chromatography) or LC-MS (Liquid Chromatography-Mass Spectrometry).

What are the potential risks or implications of having Xanomeline Impurity 4 present in a pharmaceutical product?

The presence of impurities, including Impurity 4, in pharmaceutical products can affect the safety and efficacy of the drug, leading to potential side effects or reduced therapeutic effectiveness.

How can the level of Xanomeline Impurity 4 be minimized during the production process?

The level of Xanomeline Impurity 4 can be minimized by optimizing the synthesis and purification processes, conducting thorough quality control checks, and implementing proper storage and handling protocols to prevent contamination.

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