Skip to Content
Merck
All Photos(2)

Key Documents

Safety Information

B2753

Sigma-Aldrich

Butyrylcholine chloride

≥98%

Sign Into View Organizational & Contract Pricing


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

Quality Level

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


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

B2753-5G:
B2753-10G:
B2753-VAR:
B2753-BULK:
B2753-1G:
B2753-25G:


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
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
[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)
The substrate specificity of the cholinesterase activity of the brain of the sea Pacific herring (Cluippea pallasi Val) from different populations.
N N Kovalev et al.
Doklady. Biochemistry and biophysics, 392, 256-259 (2004-07-17)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service