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1A03440

USP

Abiraterone Ethyl Ether

Pharmaceutical Analytical Impurity (PAI)

Synonyme(s) :

(3-((3S,8R,9S,10R,13S,14S)-3-ethoxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)pyridine)

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A propos de cet article

Formule empirique (notation de Hill) :
C26H35NO
Numéro CAS:
Poids moléculaire :
377.56
MDL number:
NACRES:
NA.24
UNSPSC Code:
41116107
eCl@ss:
25140904
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grade

pharmaceutical analytical impurity (PAI)

agency

USP

API family

abiraterone

manufacturer/tradename

USP

application(s)

pharmaceutical
pharmaceutical
pharmaceutical small molecule

format

neat

storage temp.

2-8°C

General description

Find answers to frequently asked questions on USP products in USP FAQs.
Abiraterone Ethyl Ether 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: Abiraterone Acetate


Therapeutic Area: Oncology

Application

Abiraterone Ethyl Ether (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.
USP issued SDS can be found here

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Cet article
1A03450PHR24101A03520
description

Pharmaceutical Analytical Impurity (PAI)

description

Pharmaceutical Analytical Impurity (PAI)

description

Pharmaceutical Secondary Standard; Certified Reference Material

description

Pharmaceutical Analytical Impurity (PAI)

grade

pharmaceutical analytical impurity (PAI)

grade

pharmaceutical analytical impurity (PAI)

grade

certified reference material, pharmaceutical secondary standard

grade

pharmaceutical analytical impurity (PAI)

manufacturer/tradename

USP

manufacturer/tradename

USP

manufacturer/tradename

-

manufacturer/tradename

USP

application(s)

pharmaceutical
pharmaceutical
pharmaceutical small molecule

application(s)

pharmaceutical
pharmaceutical
pharmaceutical small molecule

application(s)

pharmaceutical
pharmaceutical
pharmaceutical small molecule

application(s)

pharmaceutical small molecule

format

neat

format

neat

format

-

format

neat

API family

abiraterone

API family

abiraterone

API family

abiraterone

API family

-

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-30°C

storage temp.

2-8°C


Pictogrammes

Health hazardEnvironment

Mot-clé

Danger

Codes de danger

Hazard Classifications

Aquatic Chronic 1 - Repr. 1B - STOT RE 2

Organes cibles

Endocrine system

Classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Que se passe-t-il ?

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable



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