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1A00880

USP

11β,16α,17,21-Tetrahydroxypregna-1,4-dien-3,20-dion

Pharmaceutical Analytical Impurity (PAI)

Synonym(e):

16α-Hydroxyprednisolon

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Über diesen Artikel

Empirische Formel (Hill-System):
C21H28O6
CAS-Nummer:
Molekulargewicht:
376.44
MDL number:
UNSPSC Code:
41116107
NACRES:
NA.24
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grade

pharmaceutical analytical impurity (PAI)

agency

USP

API family

prednisolone

manufacturer/tradename

USP

application(s)

pharmaceutical

format

neat

storage temp.

2-8°C

SMILES string

O[C@]1([C@@]2([C@H]([C@H]3[C@@H]([C@@]4(C(=CC(=O)C=C4)CC3)C)[C@H](C2)O)C[C@H]1O)C)C(=O)CO

InChI key

SEKYBDYVXDAYPY-ILNISADRSA-N

General description

Find answers to frequently asked questions on USP products in USP FAQs.
11β,16α,17,21-Tetrahydroxypregna-1,4-dien-3,20-dione 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: Budesonide

Therapeutic Area: Steroids

For more information about this PAI, visit here.

Application

11β,16α,17,21-Tetrahydroxypregna-1,4-dien-3,20-dione (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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Dieser Artikel
PHR92281A012801A01240
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)

grade

pharmaceutical analytical impurity (PAI)

grade

TraceCERT®, certified reference material

grade

pharmaceutical analytical impurity (PAI)

grade

pharmaceutical analytical impurity (PAI)

manufacturer/tradename

USP

manufacturer/tradename

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

manufacturer/tradename

USP

manufacturer/tradename

USP

format

neat

format

-

format

neat

format

neat

application(s)

pharmaceutical

application(s)

pharmaceutical small molecule

application(s)

pharmaceutical

application(s)

pharmaceutical

API family

prednisolone

API family

prednisolone, budesonide

API family

prednisolone

API family

prednisolone

agency

USP

agency

Not traceable to any primary pharmacopeia standard

agency

USP

agency

USP


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Piktogramme

Health hazard

Signalwort

Danger

Gefahrencodes

Hazard Classifications

Repr. 1B

Lagerklasse

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

Was ist los?

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable



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