1A02550
USP
Aripiprazole Hydroxydihydroquinolinone Analog
Pharmaceutical Analytical Impurity (PAI)
Synonym(s):
7-Hydroxy-3,4-dihydro-2(1H)-quinolinone, 7-Hydroxy-1,2,3,4-tetrahydro-2-quinolinone, 7-Hydroxy-3,4-dihydrocarbostyril
About This Item
Recommended Products
grade
pharmaceutical analytical impurity (PAI)
Agency
USP
API family
aripiprazole
manufacturer/tradename
USP
mp
233-237 °C
application(s)
pharmaceutical
format
neat
storage temp.
2-8°C
SMILES string
Oc1ccc2CCC(=O)Nc2c1
InChI
1S/C9H9NO2/c11-7-3-1-6-2-4-9(12)10-8(6)5-7/h1,3,5,11H,2,4H2,(H,10,12)
InChI key
LKLSFDWYIBUGNT-UHFFFAOYSA-N
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General description
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: Aripiprazole.
For more information about this PAI, visit here.
Application
Features and Benefits
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
Other Notes
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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