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1A00880

USP

11β,16a,17,21-Tetrahydroxypregna-1,4-dien-3,20-dione

Pharmaceutical Analytical Impurity (PAI)

Sinónimos:

11β,16α,17,21-Tetrahydroxypregna-1,4-dien-3,20-dione, (8S,9S,10R,11S,13S,14S,16R,17S)-11,16,17-trihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-3-one, 16α-Hydroxyprednisolone

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Tamaño de envaseSKUDisponibilidadPrecio
25 mg
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702,00 €

Acerca de este artículo

Fórmula empírica (notación de Hill):
C21H28O6
Número CAS:
Peso molecular:
376.44
MDL number:
UNSPSC Code:
41116107
NACRES:
NA.24

702,00 €


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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

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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pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Repr. 1B

Clase de almacenamiento

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

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Número de artículo de comercio global

SKUGTIN
1A00880-25MG04065269079675

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