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1A02810

USP

Desmethyl Promethazine Hydrochloride

Pharmaceutical Analytical Impurity (PAI)

Sinónimos:

(N-methyl-1-(10H-phenothiazin-10-yl)propan-2-amine, hydrochloride)

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Talla/SKUDisponibilidadPrecio
25 mg
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1150,00 €

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Fórmula empírica (notación de Hill):
C16H18N2S · HCl
Número CAS:
MDL number:
NACRES:
NA.24
UNSPSC Code:
41116107

1150,00 €


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grade

pharmaceutical analytical impurity (PAI)

agency

USP

API family

promethazine

manufacturer/tradename

USP

application(s)

pharmaceutical
pharmaceutical
pharmaceutical small molecule

format

neat

storage temp.

2-8°C

General description

Find answers to frequently asked questions on USP products in USP FAQs.
Desmethyl Promethazine Hydrochloride 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: Promethazine


Therapeutic Area: Antihistamines

Application

Desmethyl Promethazine Hydrochloride (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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Este artículo
PHR8590Y00007691570029
description

Pharmaceutical Analytical Impurity (PAI)

description

1 mg/mL in methanol, ampule of 1 mL, certified reference material

description

European Pharmacopoeia (EP) Reference Standard

description

United States Pharmacopeia (USP) Reference Standard

manufacturer/tradename

USP

manufacturer/tradename

-

manufacturer/tradename

EDQM

manufacturer/tradename

USP

grade

pharmaceutical analytical impurity (PAI)

grade

certified reference material

grade

pharmaceutical primary standard

grade

pharmaceutical primary standard

format

neat

format

single component solution

format

neat

format

neat

application(s)

pharmaceutical small molecule

application(s)

pharmaceutical

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical

agency

USP

agency

(Not traceable to any primary pharmacopeia standard)

agency

-

agency

USP

storage temp.

2-8°C

storage temp.

-10 to -25°C

storage temp.

2-8°C

storage temp.

-


Pictogramas

Exclamation mark

Palabra de advertencia

Warning

Códigos de peligro

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

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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