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Aripiprazole Bromobutoxyquinolinone Analog

Pharmaceutical Analytical Impurity (PAI)

Synonyme(s) :

7-(4-Bromobutoxy)-2(1H)-quinolinone

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Taille/RéférenceDisponibilitéPrix
25 mg
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1 880,00 $

A propos de cet article

Formule empirique (notation de Hill) :
C13H14BrNO2
Numéro CAS:
Poids moléculaire :
296.16
NACRES:
NA.24
MDL number:
UNSPSC Code:
41116107
eCl@ss:
25140904

1 880,00 $


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grade

pharmaceutical analytical impurity (PAI)

agency

USP

API family

aripiprazole

manufacturer/tradename

USP

application(s)

pharmaceutical

format

neat

storage temp.

2-8°C

SMILES string

BrCCCCOc1cc2nc(ccc2cc1)O

InChI key

MBOHAVAGDOGRBS-UHFFFAOYSA-N

General description

Find answers to frequently asked questions on USP products in USP FAQs.
Aripiprazole Bromobutoxyquinolinone Analog 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.

Application

Aripiprazole Bromobutoxyquinolinone Analog (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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Cet article
PHR92811A024701A02560
description

Pharmaceutical Analytical Impurity (PAI)

description

certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

description

Pharmaceutical Analytical Impurity (PAI)

description

Pharmaceutical Analytical Impurity (PAI)

manufacturer/tradename

USP

manufacturer/tradename

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

manufacturer/tradename

USP

manufacturer/tradename

USP

grade

pharmaceutical analytical impurity (PAI)

grade

certified reference material, TraceCERT®

grade

pharmaceutical analytical impurity (PAI)

grade

pharmaceutical analytical impurity (PAI)

application(s)

pharmaceutical

application(s)

pharmaceutical

application(s)

pharmaceutical

application(s)

pharmaceutical
pharmaceutical
pharmaceutical small molecule

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

agency

USP

agency

Not traceable to any primary pharmacopeia standard

agency

USP

agency

USP


Classe de stockage

11 - Combustible Solids

WGK

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable



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