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Diamide Sitagliptin impurity

(S)-N-acetyl-N-(4-oxo-4-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)-1-(2,4,5-trifluorophenyl)butan-2-yl)acetamide;

Specifications:

CAS No.

Mol F.

: C20H19F6N5O3

Mol W.

: 491.39

Cat No.

: SA10420

Appearance

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Product Name

: Diamide Sitagliptin impurity

CAS No.

Mol F.

: C20H19F6N5O3

Mol W.

: 491.39

Cat No.

: SA10420

Appearance

Synonyms

: (S)-N-acetyl-N-(4-oxo-4-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)-1-(2,4,5-trifluorophenyl)butan-2-yl)acetamide;

Related API

: Sitagliptin

Category

Diamide Sitagliptin impurity product with CAS: NA is also known as (S)-N-acetyl-N-(4-oxo-4-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)-1-(2,4,5-trifluorophenyl)butan-2-yl)acetamide. This product can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. Diamide Sitagliptin impurity is generally used for Quality Control (QC), Quality Assurance (QA) during commercial production of Sitagliptin and its related formulations. Moreover, (S)-N-acetyl-N-(4-oxo-4-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)-1-(2,4,5-trifluorophenyl)butan-2-yl)acetamide is also used in the process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation.

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