Fimasartan Impurity A

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For Research Use Only | Not For Clinical Use

CAT	APB1315478137
CAS	1315478-13-7
Synonyms	2-(2-butyl-4-methyl-6-oxo-1,6-dihydropyrimidin-5-yl)-N,N-dimethylacetamide
Molecular Weight	251.32
Molecular Formula	C13H21N3O2

What is the product name of Fimasartan Impurity A?

The product name of Fimasartan Impurity A is 2-(2-butyl-4-methyl-6-oxo-1,6-dihydropyrimidin-5-yl)-N,N-dimethylacetamide.

What is the CAS number of Fimasartan Impurity A?

The CAS number of Fimasartan Impurity A is 1315478-13-7.

What are the synonyms of Fimasartan Impurity A?

One of the synonyms is 2-(2-butyl-4-methyl-6-oxo-1,6-dihydropyrimidin-5-yl)-N,N-dimethylacetamide.

What is the molecular weight of Fimasartan Impurity A?

The molecular weight of Fimasartan Impurity A is 251.32.

What is the molecular formula of Fimasartan Impurity A?

The molecular formula of Fimasartan Impurity A is C13H21N3O2.

What are the structural components of Fimasartan Impurity A?

The structural components of Fimasartan Impurity A are 1,6-dihydropyrimidin-5-yl, butyl, methyl, and dimethylacetamide.

Why is it important to identify and characterize impurities in pharmaceutical compounds such as Fimasartan Impurity A?

It is important to identify and characterize impurities in pharmaceutical compounds to ensure product quality, safety, and efficacy.

How can Fimasartan Impurity A be detected and quantified in pharmaceutical formulations?

Fimasartan Impurity A can be detected and quantified using analytical techniques such as HPLC or LC-MS.

What are the potential sources of Fimasartan Impurity A in pharmaceutical manufacturing processes?

Potential sources of Fimasartan Impurity A in pharmaceutical manufacturing processes include starting materials, reagents, intermediates, and process impurities.

How can the presence of Fimasartan Impurity A impact the stability and shelf life of pharmaceutical products?

The presence of Fimasartan Impurity A can impact the stability and shelf life of pharmaceutical products by potentially compromising the quality, potency, and safety of the final formulation.

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