Brexpiprazole Impurity 26

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For Research Use Only | Not For Clinical Use

CAT	APB79145598
CAS	79145-59-8
Molecular Weight	237.68
Molecular Formula	C12H12ClNO2

What is the product name of CAS 79145-59-8?

The product name is Brexpiprazole Impurity 26.

What is the molecular weight of Brexpiprazole Impurity 26?

The molecular weight is 237.68.

What is the molecular formula of Brexpiprazole Impurity 26?

The molecular formula is C12H12ClNO2.

What is the chemical structure of Brexpiprazole Impurity 26?

The chemical structure is made up of 12 carbon atoms, 12 hydrogen atoms, 1 chlorine atom, 1 nitrogen atom, and 2 oxygen atoms.

What is the significance of Impurity 26 in the production of Brexpiprazole?

Impurity 26 is a byproduct or contaminant that may be present in Brexpiprazole, which can impact the purity and quality of the final product.

How is Brexpiprazole Impurity 26 identified and quantified in the manufacturing process?

Brexpiprazole Impurity 26 is identified and quantified through analytical techniques such as chromatography, spectroscopy, or mass spectrometry.

What potential effects could Brexpiprazole Impurity 26 have on the efficacy of Brexpiprazole?

The presence of Impurity 26 could potentially affect the potency, stability, or safety profile of Brexpiprazole, leading to concerns about its efficacy.

How is Brexpiprazole Impurity 26 synthesized in the production of Brexpiprazole?

Impurity 26 may be generated as a result of the chemical reactions involved in the synthesis of Brexpiprazole, or it may be introduced during the purification or formulation processes.

What measures can be taken to minimize the presence of Brexpiprazole Impurity 26 in the final product?

Stringent quality control measures, purification techniques, and regular monitoring of impurity levels can help minimize the presence of Impurity 26 in Brexpiprazole.

Are there regulations or guidelines in place regarding the allowable levels of Brexpiprazole Impurity 26 in pharmaceutical products?

Regulatory authorities such as the FDA or EMA may have set limits on the acceptable levels of impurities, including Impurity 26, in pharmaceutical products to ensure safety and quality standards are met.

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