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1A00190

USP

QUETIAPINE DESETHOXY

Pharmaceutical Analytical Impurity (PAI)

Synonym(e):

Quetiapine Desethoxy, (2-[4-(dibenzo[b,f][1,4]thiazepin-11-yl)piperazin-1-yl]ethanol)

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Über diesen Artikel

Empirische Formel (Hill-System):
C19H21N3OS
CAS-Nummer:
Molekulargewicht:
339.45
MDL number:
NACRES:
NA.24
UNSPSC Code:
41116107
eCl@ss:
25140904
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grade

pharmaceutical analytical impurity (PAI)

agency

USP

API family

quetiapine

manufacturer/tradename

USP

application(s)

pharmaceutical
pharmaceutical
pharmaceutical small molecule

format

neat

storage temp.

2-8°C

SMILES string

[s]1c2c(nc(c4c1cccc4)N3CCN(CC3)CCO)cccc2

InChI

1S/C19H21N3OS/c23-14-13-21-9-11-22(12-10-21)19-15-5-1-3-7-17(15)24-18-8-4-2-6-16(18)20-19/h1-8,23H,9-14H2

InChI key

OFLMIXVKBNAUIB-UHFFFAOYSA-N

General description

Find answers to frequently asked questions on USP products in USP FAQs.
QUETIAPINE DESETHOXY 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: Quetiapine fumarate
Therapeutic Area: Psychiatrics

Application

QUETIAPINE DESETHOXY (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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Dieser Artikel
15927921A00180
description

Pharmaceutical Analytical Impurity (PAI)

description

United States Pharmacopeia (USP) Reference Standard

description

Pharmaceutical Analytical Impurity (PAI)

application(s)

pharmaceutical
pharmaceutical
pharmaceutical small molecule

application(s)

pharmaceutical

application(s)

pharmaceutical small molecule

format

neat

format

neat

format

neat

grade

pharmaceutical analytical impurity (PAI)

grade

pharmaceutical primary standard

grade

pharmaceutical analytical impurity (PAI)

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

manufacturer/tradename

USP

manufacturer/tradename

USP

manufacturer/tradename

USP

agency

USP

agency

USP

agency

USP


Piktogramme

Health hazardExclamation mark

Signalwort

Warning

Gefahrencodes

Hazard Classifications

Acute Tox. 4 Oral - Repr. 2 - STOT SE 3

Zielorgane

Central nervous system

Lagerklasse

10 - Combustible liquids

Was ist los?

WGK 1



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