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1A02630

USP

(S)-Sitagliptin Phosphate

Pharmaceutical Analytical Impurity (PAI)

Synonym(e):

(S)-Sitagliptin Phosphate, (S)-3-amino-1-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)-4-(2,4,5-trifluorophenyl)butan-1-one phosphate

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Über diesen Artikel

Empirische Formel (Hill-System):
C16H18F6N5O5P
CAS-Nummer:
Molekulargewicht:
505.31
MDL number:
UNSPSC Code:
41116107
NACRES:
NA.24
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grade

pharmaceutical analytical impurity (PAI)

agency

USP

API family

sitagliptin

manufacturer/tradename

USP

application(s)

pharmaceutical

format

neat

storage temp.

2-8°C

SMILES string

FC(F)(F)c1[n]2c(nn1)CN(CC2)C(=O)C[C@@H](N)Cc3c(cc(c(c3)F)F)F.[P](=O)(=O)OO.[HH]

InChI

1S/C16H15F6N5O.HO4P.H2/c17-10-6-12(19)11(18)4-8(10)3-9(23)5-14(28)26-1-2-27-13(7-26)24-25-15(27)16(20,21)22;1-4-5(2)3;/h4,6,9H,1-3,5,7,23H2;1H;1H/t9-;;/m0../s1

InChI key

SHWZYHNHAUKDOV-WWPIYYJJSA-N

General description

Find answers to frequently asked questions on USP products in USP FAQs.
(S)-(+)-N-(2,3-Epoxypropyl)phthalimide is a USP Pharmaceutical Analytical Impurity (PAI).

USP PAI are a product line of impurities suitable for research and analytical purposes, which help to ensure the quality and safety of medicines.

Associated Drug Substance: Sitagliptin

For more information about this PAI, visit here.

Application

(S)-(+)-N-(2,3-Epoxypropyl)phthalimide (USP PAI) is intended for use in analytical testing to detect, identify, and measure pharmaceutical impurities.

Features and Benefits

USP PAI advance your early analytical R&D and process development. PAI can be used in the following applications:

1. Conduct analytical tests during early formulation feasibility studies.
2. Determine degradation impurities produced during stress studies.
3. Develop, validate, and transfer analytical methods.
4. Perform spiking studies during process R&D to demonstrate depletion upon recrystallization.
5. Record retention times and/or spectra
6. Determine relative response factors.
7. Identify unknown impurities that formed during ICH stability conditions.
8. Identify impurities that are present in the Reference Listed Drug
9. Test for and profile impurities not listed in drug substance and drug product monographs.

Analysis Note

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  

Other Notes

Sales restrictions may apply.

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Dieser Artikel
PHR32711A015401A02590
description

Pharmaceutical Analytical Impurity (PAI)

description

pharmaceutical secondary standard, certified reference material

description

Pharmaceutical Analytical Impurity (PAI)

description

Pharmaceutical Analytical Impurity (PAI)

grade

pharmaceutical analytical impurity (PAI)

grade

certified reference material, pharmaceutical secondary standard

grade

pharmaceutical analytical impurity (PAI)

grade

pharmaceutical analytical impurity (PAI)

manufacturer/tradename

USP

manufacturer/tradename

-

manufacturer/tradename

USP

manufacturer/tradename

USP

application(s)

pharmaceutical

application(s)

pharmaceutical

application(s)

pharmaceutical

application(s)

pharmaceutical

format

neat

format

-

format

neat

format

neat

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

API family

sitagliptin

API family

sitagliptin

API family

-

API family

piperazine


Piktogramme

Exclamation mark

Signalwort

Warning

Gefahrencodes

Hazard Classifications

Skin Irrit. 2

Lagerklasse

11 - Combustible Solids

Was ist los?

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable



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