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Sitagliptin Tablets EP Impurity FP-A(Mix.of Diastereomers)

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COA COO

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Sitagliptin Tablets EP Impurity FP-A(Mix.of Diastereomers)

Impurity

CAS Number

2088771-60-0

Molecular Formula

C20H19F6N5O5

Product format

Neat

Molecular Weight

523.39

Storage

-20°C

Shipping

Room Temperature

API Family

Sitagliptin

Synonyms

((R)-4-oxo-4-(3-(trifluoromethyl)-5, 6-dihydro-[1, 2, 4]triazolo[4, 3-a]pyrazin-7(8H)-yl)-1-(2, 4 and 5-trifluorophenyl)butan-2-yl)aspartic acid

Iupac Name

2-[[(2R)-4-oxo-4-[3-(trifluoromethyl)-6, 8-dihydro-5H-[1, 2, 4]triazolo[4, 3-a]pyrazin-7-yl]-1-(2, 4 and 5-trifluorophenyl)butan-2-yl]amino]butanedioic acid

InChI

InChI=1S/C20H19F6N5O5/c21-11-6-13(23)12(22)4-9(11)3-10(27-14(18(35)36)7-17(33)34)5-16(32)30-1-2-31-15(8-30)28-29-19(31)20(24,25)26/h4,6,10,14,27H,1-3,5,7-8H2,(H,33,34)(H,35,36)/t10-,14?/m1/s1

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Available products

Pack Size SKU
Category Expected Delivery Price Quantity
25mg
CE4070.86-25MG

3-4 weeks

25mg
CD4070.86-25MG

3-5 weeks

25mg
CB4070.86-25MG

4-5 weeks

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Product Type

Impurity

Our Impurity Characterized Standards portfolio comprises more than 5,000 compounds accompanied by a comprehensive CoA which can be found in 3 product categories that include a set of different analytical techniques for determining Identity and Purity.

API

We have designed a range of primary API standards manufactured according to international regulations that come with the most extensive Certificate of Analysis which includes Identity checks by several techniques.

Excipient

Excipients standards comes with a detailed Certificate of Analysis with Identity, Purity and Assay data. They are also suitable for use with non-compendial analytical methods.

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Synthesis

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