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1269221

USP

Famotidine Related Compound B

United States Pharmacopeia (USP) Reference Standard

Sinónimos:

N,N′′′-[(1,1-Dioxido-2H-1,2,4,6-thiatriazine-3,5-diyl)bis(2,1-ethanediylthiomethylene-4,2-thiazolediyl)]bisguanidine, 3,5-Bis[2-[[[2-[(diaminomethylene)amino]thiazol-4-yl]methyl]sulphanyl]ethyl]-4H-1,2,4,6-thiatriazine 1,1-dioxide

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Tamaño de envaseSKUDisponibilidadPrecio
25 mg
Comprobar disponibilidad del carrito
$1.400.000

Acerca de este artículo

Fórmula empírica (notación de Hill):
C16H23N11O2S5
Número CAS:
Peso molecular:
561.75
MDL number:
UNSPSC Code:
41116107
NACRES:
NA.24

$1.400.000


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biological source

synthetic

grade

pharmaceutical primary standard

agency

USP

API family

famotidine

form

powder

packaging

pkg of 25 mg

manufacturer/tradename

USP

storage condition

protect from light

color

yellow to white

solubility

water: soluble

application(s)

pharmaceutical (small molecule)

format

neat

InChI

1S/C16H23N11O2S5/c17-13(18)24-15-21-9(7-32-15)5-30-3-1-11-23-12(27-34(28,29)26-11)2-4-31-6-10-8-33-16(22-10)25-14(19)20/h7-8H,1-6H2,(H,23,26,27)(H4,17,18,21,24)(H4,19,20,22,25)

InChI key

NRRXZFHNRLQONH-UHFFFAOYSA-N

General description

Famotidine Related Compound B (Famotidine Impurity B) is an impurity of famotidine, which is a hydrophilic, cationic, histamine H2 receptor antagonist drug that effectively inhibits gastric acid secretion in humans.

Application

Famotidine Related Compound B USP reference standard, intended for use in specified quality tests and assays as specified in the USP compendia. Also, for use with USP monograph such as Famotidine

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
PHR2912PHR29091269265
grade

pharmaceutical primary standard

grade

pharmaceutical secondary standard, reference material

grade

certified reference material, pharmaceutical secondary standard

grade

pharmaceutical primary standard

manufacturer/tradename

USP

manufacturer/tradename

-

manufacturer/tradename

-

manufacturer/tradename

USP

form

powder

form

-

form

solid

form

powder

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical small molecule

application(s)

pharmaceutical small molecule

application(s)

pharmaceutical (small molecule)

format

neat

format

-

format

-

format

neat

storage condition

protect from light

storage condition

-

storage condition

-

storage condition

protect from light


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Clase de almacenamiento

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable



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Certificados de análisis (COA)

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High-performance thin-layer chromatography for the determination of ranitidine hydrochloride and famotidine in pharmaceuticals.
Novakovic J.
Journal of Chromatography A, 846(1-2), 193-198 (1999)
Capillary zone electrophoresis method for the determination of famotidine and related impurities in pharmaceuticals
Helali N, et al.
Talanta, 74(4) (2008)
Famotidine
Pharmacopeia, US
United States Pharmacopeia, 39(1)(1-2), 1815-1815 (2020)



Número de artículo de comercio global

SKUGTIN
1269221-25MG04061833830215

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