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1A04400

USP

N-NITROSOIMINODIACETIC ACID

Pharmaceutical Analytical Impurity (PAI)

Sinónimos:

N-nitrosoiminodiacetic acid, (2,2′-(Nitrosoazanediyl)diacetic acid)

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Fórmula empírica (notación de Hill):
C4H6N2O5
Número CAS:
Peso molecular:
162.10
MDL number:
NACRES:
NA.24
UNSPSC Code:
41116107
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grade

pharmaceutical analytical impurity (PAI)

agency

USP

manufacturer/tradename

USP

application(s)

pharmaceutical
pharmaceutical
pharmaceutical small molecule

format

neat

storage temp.

-10 to -25°C

General description

Find answers to frequently asked questions on USP products in USP FAQs.
N-Nitrosoiminodiacetic 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.

For more information about this PAI, visit here.

Application

N-Nitrosoiminodiacetic Acid 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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Este artículo
1A040701A02580442687
description

Pharmaceutical Analytical Impurity (PAI)

description

Pharmaceutical Analytical Impurity (PAI)

description

Pharmaceutical Analytical Impurity (PAI)

description

analytical standard

grade

pharmaceutical analytical impurity (PAI)

grade

pharmaceutical analytical impurity (PAI)

grade

pharmaceutical analytical impurity (PAI)

grade

analytical standard

manufacturer/tradename

USP

manufacturer/tradename

USP

manufacturer/tradename

USP

manufacturer/tradename

-

application(s)

pharmaceutical small molecule

application(s)

pharmaceutical small molecule

application(s)

pharmaceutical small molecule

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

format

(solution)

format

neat

format

neat

agency

USP

agency

USP

agency

USP

agency

-

storage temp.

-10 to -25°C

storage temp.

−20°C

storage temp.

-10 to -25°C

storage temp.

2-30°C


Clase de almacenamiento

11 - Combustible Solids

Punto de inflamación (°F)

Not applicable

Punto de inflamación (°C)

Not applicable



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