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1623604

USP

Succinylmonocholine chloride

United States Pharmacopeia (USP) Reference Standard

Sinónimos:

2-(3-Carboxy-1-oxopropoxy)-N,N,N-trimethylethanaminium chloride

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About This Item

Fórmula empírica (notación de Hill):
C9H18ClNO4
Número de CAS:
Peso molecular:
239.70
Número MDL:
Código UNSPSC:
41116107
NACRES:
NA.24

grado

pharmaceutical primary standard

familia API

succinylcholine

fabricante / nombre comercial

USP

aplicaciones

pharmaceutical (small molecule)

Formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

Cl.[N+](CCOC(=O)CCC(=O)[O-])(C)(C)C

InChI

1S/C9H17NO4.ClH/c1-10(2,3)6-7-14-9(13)5-4-8(11)12;/h4-7H2,1-3H3;1H

Clave InChI

LDHMZIUMVSRSIK-UHFFFAOYSA-N

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Descripción general

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Aplicación

Succinylmonocholine chloride 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 Succinylcholine Chloride

Nota de análisis

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.  ​

Otras notas

Sales restrictions may apply.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Succinylmonocholine identified in negative control tissues.
Marc LeBeau et al.
Journal of analytical toxicology, 27(8), 600-601 (2003-12-17)
M M Andrews et al.
The Journal of pharmacy and pharmacology, 39(3), 173-179 (1987-03-01)
The effects of equimolar concentrations (3.0 X 10(-5) M) of succinylcholine (SCh) and succinylmonocholine (SMC) were studied in-vitro at 20 degrees C in rat extensor digitorum longus muscle (EDL) 0-147 days after common peroneal nerve section. Analysis of simultaneous measurements
Uta Kuepper et al.
Rapid communications in mass spectrometry : RCM, 22(12), 1965-1970 (2008-05-21)
The determination and quantitation of drugs in biological matrices using high-performance liquid chromatography/tandem mass spectrometry (HPLC/MS/MS) is becoming increasingly popular in analytical toxicology, while at the same time a growing awareness for the limits of this technique can be observed.
Uta Kuepper et al.
International journal of legal medicine, 126(2), 259-269 (2011-09-29)
The muscle relaxant succinylcholine (SUX) evokes respiratory paralysis, and numerous cases of fatal SUX intoxication have been reported. Detection of SUX and its metabolite succinylmonocholine (SMC) is difficult, both due to their (bis-) quaternary structure and the extreme hydrolytic susceptibility
I Yasuda et al.
Anesthesiology, 57(4), 289-292 (1982-10-01)
The mechanism of bradycardia caused by the administration of succinylcholine has not been fully elucidated. Accordingly, the effects of succinylcholine and succinylmonocholine on the sinoatrial node were studied in 35 mongrel dogs. The sinus node artery was selectively perfused with

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