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USP

3-(1-Cyanoethyl)benzoic acid

Pharmaceutical Analytical Impurity (PAI)

Synonim(y):

2-(3-Carboxyphenyl)Propionitrile

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Rozmiar/SKUDostępnośćCena netto
25 mg
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3640,00 zł

Informacje o tej pozycji

Wzór liniowy:
CH3CH(CN)C6H4CO2H
Numer CAS:
Masa cząsteczkowa:
175.18
NACRES:
NA.24
MDL number:
UNSPSC Code:
41116107

3640,00 zł


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grade

pharmaceutical analytical impurity (PAI)

agency

USP

manufacturer/tradename

USP

mp

145-148 °C (lit.)

application(s)

pharmaceutical

format

neat

storage temp.

2-8°C

SMILES string

CC(C#N)c1cccc(c1)C(O)=O

InChI

1S/C10H9NO2/c1-7(6-11)8-3-2-4-9(5-8)10(12)13/h2-5,7H,1H3,(H,12,13)

InChI key

IRYIYPWRXROPSX-UHFFFAOYSA-N

General description

Find answers to frequently asked questions on USP products in USP FAQs.
3-(1-Cyanoethyl)benzoic acid 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: Ketoprofen.

For more information about this PAI, visit here.

Application

3-(1-Cyanoethyl)benzoic acid (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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CRM4227910817501460328
description

Pharmaceutical Analytical Impurity (PAI)

description

Certified Reference Material

description

United States Pharmacopeia (USP) Reference Standard

description

United States Pharmacopeia (USP) Reference Standard

manufacturer/tradename

USP

manufacturer/tradename

-

manufacturer/tradename

USP

manufacturer/tradename

USP

grade

pharmaceutical analytical impurity (PAI)

grade

pharmaceutical secondary standard, certified reference material

grade

pharmaceutical primary standard

grade

pharmaceutical primary standard

application(s)

pharmaceutical

application(s)

-

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecules)

format

neat

format

-

format

neat

format

neat

agency

USP

agency

-

agency

USP

agency

USP

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C


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pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Sens. 1

Klasa składowania

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable



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