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D1260

Sigma-Aldrich

Decamethoniumbromid

crystalline

Synonym(e):

Decamethylen-bis(trimethylammoniumbromid), Decan-1,10-bis-trimethylammoniumbromid

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About This Item

Lineare Formel:
(CH3)3N(Br)(CH2)10N(Br)(CH3)3
CAS-Nummer:
541-22-0
Molekulargewicht:
418.29
Beilstein:
3728288
EG-Nummer:
208-772-2
MDL-Nummer:
MFCD00011779
UNSPSC-Code:
12352200
PubChem Substanz-ID:
24277833
NACRES:
NA.77

Form

crystalline

Qualitätsniveau

200

Farbe

off-white

mp (Schmelzpunkt)

263-267 °C (lit.)

Ersteller

GlaxoSmithKline

SMILES String

[Br-].[Br-].C[N+](C)(C)CCCCCCCCCC[N+](C)(C)C

InChI

1S/C16H38N2.2BrH/c1-17(2,3)15-13-11-9-7-8-10-12-14-16-18(4,5)6;;/h7-16H2,1-6H3;2*1H/q+2;;/p-2

InChIKey

HLXQFVXURMXRPU-UHFFFAOYSA-L

Angaben zum Gen

human ... CHRNA1(1134) , CHRNA10(57053) , CHRNA2(1135) , CHRNA3(1136) , CHRNA4(1137) , CHRNA5(1138) , CHRNA6(8973) , CHRNA7(1139) , CHRNA9(55584) , CHRNB1(1140) , CHRNB2(1141) , CHRNB3(1142) , CHRNB4(1143) , CHRND(1144) , CHRNE(1145) , CHRNG(1146)

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Anwendung

Decamethonium bromide has been used to induce paralysis in duck embryo.

Biochem./physiol. Wirkung

Nicotinic acetylcholine receptor partial agonist and neuromuscular blocking agent; depolarizes striated muscles and blocks their activity.
Decamethonium serves as a muscle relaxant and is also a neuromuscular blocking agent. It has a molecular weight of 258.4.

Leistungsmerkmale und Vorteile

This compound was developed by GlaxoSmithKline. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Piktogramme

Skull and crossbones
GHS06

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Analysenzertifikate (COA)

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Dodecyltrimethylammoniumbromid ≥98%

Sigma-Aldrich

D8638

Dodecyltrimethylammoniumbromid

D Bertrand et al.
Proceedings of the National Academy of Sciences of the United States of America, 87(5), 1993-1997 (1990-03-01)
Neuronal nicotinic acetylcholine receptor of the alpha 4/non-alpha (alpha 4/n alpha) type was reconstituted in Xenopus oocytes after nuclear injection of cDNA expression vectors. Functional neuronal receptor was only formed when the two subunits alpha 4 and n alpha were
Mesenchymal and mechanical mechanisms of secondary cartilage induction
Solem R C, et al.
Developmental Biology, 356(1), 28-39 (2011)
Amina S Woods et al.
Journal of proteome research, 7(8), 3423-3427 (2008-06-27)
We have previously used MALDI mass spectrometry to highlight ammonium- or guanidinium-aromatic interactions via cation-pi bonding and ammonium- or guanidinium-phosphate interactions through salt bridge formation. In the present work, the gas-phase stability and dissociation pathways of the interaction between phosphorylated
L N Lisetski et al.
European biophysics journal : EBJ, 31(7), 554-558 (2003-02-27)
We have studied the action of some membranotropic agents (MTAs) on the parameters of mono- and multilayers of dipalmitoylphosphatidylcholine (DPPC). The MTAs used included an antimicrobial drug, decamethoxinum, the model amphiphilic agent stearoyl-L-alpha-alanine, and cholesterol as a reference substance. Using
V A Pashynskaya et al.
Rapid communications in mass spectrometry : RCM, 16(18), 1706-1713 (2002-09-11)
Mechanisms of interaction between the antimicrobial drugs decamethoxinum and aethonium, which are based on bisquaternary ammonium compounds, and a phospholipid component of biological membranes, dipalmitoylphosphatidylcholine, were studied by means of liquid secondary ion mass spectrometry (LSIMS) and differential scanning calorimetry
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