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USP

Fexofenadine N-oxide

United States Pharmacopeia (USP) Reference Standard

Synonim(y):

(1-(4-(4-(2-carboxypropan-2-yl)phenyl)-4-hydroxybutyl)-4-(hydroxydiphenylmethyl)piperidine 1-oxide)

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Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C32H39NO5
Numer CAS:
Masa cząsteczkowa:
517.66
UNSPSC Code:
41116107
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grade

pharmaceutical primary standard

agency

USP

manufacturer/tradename

USP

application(s)

pharmaceutical small molecule

format

neat

storage temp.

-10 to -25°C

General description

Fexofenadine N-Oxide 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: Fexofenadine


Therapeutic Area: Antihistamines

Application

Fexofenadine N-Oxide 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.
USP issued SDS can be found here
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127039912703881270363
USP

USP

1270363

Fexofenadine

description

United States Pharmacopeia (USP) Reference Standard

description

United States Pharmacopeia (USP) Reference Standard

description

United States Pharmacopeia (USP) Reference Standard

description

-

application(s)

pharmaceutical small molecule

application(s)

pharmaceutical
pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)
pharmaceutical

application(s)

-

format

neat

format

neat

format

neat

format

neat

grade

pharmaceutical primary standard

grade

pharmaceutical primary standard

grade

pharmaceutical primary standard

grade

pharmaceutical primary standard

storage temp.

-10 to -25°C

storage temp.

-

storage temp.

-

storage temp.

2-30°C

manufacturer/tradename

USP

manufacturer/tradename

USP

manufacturer/tradename

USP

manufacturer/tradename

USP

agency

USP

agency

USP

agency

USP

agency

USP


Klasa składowania

11 - Combustible Solids

Co się dzieje?

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable



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Certyfikaty analizy (CoA)

Lot/Batch Number

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