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Key Documents

B2753

Sigma-Aldrich

Butyrylcholine chloride

≥98%

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About This Item

Linear Formula:
C9H20NO2Cl
CAS Number:
Molecular Weight:
209.71
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

≥98%

form

powder

storage temp.

−20°C

SMILES string

O.[Cl-].CCCC(=O)OCC[N+](C)(C)C

InChI

1S/C9H20NO2.ClH/c1-5-6-9(11)12-8-7-10(2,3)4;/h5-8H2,1-4H3;1H/q+1;/p-1

InChI key

VCOBYGVZILHVOO-UHFFFAOYSA-M

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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G Petroianu et al.
Journal of toxicology. Clinical toxicology, 39(1), 27-31 (2001-05-01)
Intoxications with organophosphorous compounds, especially paraoxon, are frequent. Organophosphorous compounds inhibit serine hydrolases such as acetylcholine, butyrilcholine, and carboxyl esterases although acetylcholine and butyrylcholine are too sensitive to paraoxon to be useful markers of severity. They cannot show a dose-dependent
S Darvesh et al.
Journal of the autonomic nervous system, 71(2-3), 75-84 (1998-10-06)
Cholinergic neurotransmission plays a significant role in intrinsic cardiac ganglia with the action of acetylcholine being terminated by acetylcholinesterase (AChE, EC 3.1.1.7). Anatomical studies were performed to characterize neurons associated with AChE and a closely related enzyme, butyrylcholinesterase (BuChE, EC
[Treatment of Alzheimer's disease: status quo and future considerations].
Shun Shimohama
Nihon yakurigaku zasshi. Folia pharmacologica Japonica, 131(5), 351-356 (2008-05-16)
Sultan Darvesh et al.
Experimental neurology, 188(2), 461-470 (2004-07-13)
Cholinesterase inhibitors used to treat the symptoms of Alzheimer's disease (AD) inhibit both acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE), albeit to different degrees. Because central and peripheral neurons, including intrinsic cardiac neurons located on the surface of the mammalian heart, express
A L Gindilis et al.
Prikladnaia biokhimiia i mikrobiologiia, 34(3), 326-331 (1998-06-30)
Potentiometric choline electrodes were developed on the basis of the mediator-free bioelectrocatalysis. The electrodes made of a composite carbon-polymer material contain choline oxidase and peroxidase coimmobilized on the surface of the electrode. The rate of the potential increase was shown

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