1A02420
USP
Aripiprazole Diquinolinone Butanediol
Pharmaceutical Analytical Impurity (PAI)
Sinônimo(s):
(7,7′-(butane-1,4-diylbis(oxy))bis(3,4-dihydroquinolin-2(1H)-one))
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About This Item
Fórmula empírica (Notação de Hill):
C22H24N2O4
Número CAS:
Peso molecular:
380.44
Código UNSPSC:
41116100
NACRES:
NA.24
Produtos recomendados
grau
pharmaceutical analytical impurity (PAI)
Agency
USP
família API
aripiprazole
fabricante/nome comercial
USP
aplicação(ões)
pharmaceutical
formato
neat
temperatura de armazenamento
2-8°C
Categorias relacionadas
Descrição geral
Aripiprazole Diquinolinone Butanediol 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: Aripiprazole.
For more information about this PAI, visit here.
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.
Aplicação
Aripiprazole Diquinolinone Butanediol (USP PAI) is intended for use in analytical testing to detect, identify, and measure pharmaceutical impurities.
Características e benefícios
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.
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.
Nota de análise
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.
Outras notas
Sales restrictions may apply.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Certificados de análise (COA)
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