Sparsentan impurity 5

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For Research Use Only | Not For Clinical Use

CAT	APB948349664
CAS	948349-66-4
Molecular Weight	287.15
Molecular Formula	C12H15BrO3

What is the specific name of the impurity known as CAS 948349-66-4?

The impurity is known as Sparsentan impurity 5, with a CAS number of 948349-66-4.

What is the molecular weight of Sparsentan impurity 5?

The molecular weight of Sparsentan impurity 5 is 287.15.

What is the molecular formula of Sparsentan impurity 5?

The molecular formula of Sparsentan impurity 5 is C12H15BrO3.

What can be inferred about the chemical composition of Sparsentan impurity 5 based on its molecular formula?

Based on the molecular formula C12H15BrO3, it can be inferred that the impurity contains 12 carbon atoms, 15 hydrogen atoms, and 1 bromine atom.

How can Sparsentan impurity 5 be identified in a chemical analysis?

Sparsentan impurity 5 can be identified in a chemical analysis based on its specific CAS number, molecular weight, and molecular formula.

Is Sparsentan impurity 5 a common impurity found in pharmaceutical products?

The presence of Sparsentan impurity 5 in pharmaceutical products would depend on the specific synthesis and production process. it may or may not be a common impurity based on these factors.

What potential effects could the presence of Sparsentan impurity 5 have on the quality of a pharmaceutical product?

The presence of impurities in pharmaceutical products can affect their potency, safety, and stability. therefore, it is important to control and monitor impurities like Sparsentan impurity 5.

Are there specific guidelines or regulations regarding the allowable levels of Sparsentan impurity 5 in pharmaceutical products?

Regulatory bodies such as the FDA may have guidelines on impurity levels in pharmaceutical products, including Sparsentan impurity 5. these guidelines are typically based on safety and efficacy considerations.

How may the synthesis and purification process of Sparsentan impurity 5 be optimized to reduce impurities?

Optimizing the synthesis and purification process may involve using high-quality starting materials, controlling reaction conditions, and employing efficient purification techniques to minimize impurities.

What analytical methods can be used to detect and quantify Sparsentan impurity 5 in pharmaceutical products?

Analytical methods such as HPLC (High-Performance Liquid Chromatography) or GC-MS (Gas Chromatography-Mass Spectrometry) can be used to detect and quantify impurities like Sparsentan impurity 5 in pharmaceutical products.

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