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1A00490

USP

Amoxicilloic Acid Dimers 1 And 2

Pharmaceutical Analytical Impurity (PAI)

Sinónimos:

((4S)-2-[1-[[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino]-2-[[(1R)-2-[[carboxy[(4S)-4-carboxy-5,5-dimethyl-1,3- thiazolidin-2-yl]methyl]amino]-1-(4-hydroxyphenyl)-2-oxoethyl]amino]-2-oxoethyl]-5,5-dimethyl-1,3-thiazolidine-4- carboxylic Acid)

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Talla/SKUDisponibilidadPrecio
10 mg
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1350,00 €

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Fórmula empírica (notación de Hill):
C32H40N6O11S2
Número CAS:
Peso molecular:
748.82
NACRES:
NA.24
UNSPSC Code:
41116107

1350,00 €


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grade

pharmaceutical analytical impurity (PAI)

agency

USP

manufacturer/tradename

USP

application(s)

pharmaceutical

format

neat

storage temp.

−20°C

General description

Find answers to frequently asked questions on USP products in USP FAQs.
Amoxicilloic Acid Dimers 1 And 2 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: Amoxicillin

Therapeutic Area: Antibiotics.

For more information about this PAI, visit here.

Application

Amoxicilloic Acid Dimers 1 And 2 (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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Este artículo
1A003301031503PHR2192
description

Pharmaceutical Analytical Impurity (PAI)

description

Pharmaceutical Analytical Impurity (PAI)

description

United States Pharmacopeia (USP) Reference Standard

description

Pharmaceutical Secondary Standard; Certified Reference Material

grade

pharmaceutical analytical impurity (PAI)

grade

pharmaceutical analytical impurity (PAI)

grade

pharmaceutical primary standard

grade

pharmaceutical secondary standard, certified reference material

manufacturer/tradename

USP

manufacturer/tradename

USP

manufacturer/tradename

USP

manufacturer/tradename

-

application(s)

pharmaceutical

application(s)

pharmaceutical small molecule

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical small molecule

format

neat

format

neat

format

neat

format

-

agency

USP

agency

USP

agency

USP

agency

traceable to USP 1031558

storage temp.

−20°C

storage temp.

-10 to -25°C

storage temp.

−20°C

storage temp.

-10 to -25°C


Clase de almacenamiento

11 - Combustible Solids

¿Qué está pasando?

WGK 3

Punto de inflamación (°F)

Not applicable

Punto de inflamación (°C)

Not applicable



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