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Merck
CN

B121

Bromoacetylcholine bromide

Synonym(s):

2-(2-Bromoacetyloxy)-N.,N,N-trimethylethanaminium bromide

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About This Item

Empirical Formula (Hill Notation):
C7H15BrNO2 · Br
CAS Number:
Molecular Weight:
305.01
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
Form:
powder
Quality level:
Technical Service
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form

powder

Quality Level

solubility

H2O: soluble

storage temp.

−20°C

SMILES string

[Br-].C[N+](C)(C)CCOC(=O)CBr

InChI

1S/C7H15BrNO2.BrH/c1-9(2,3)4-5-11-7(10)6-8;/h4-6H2,1-3H3;1H/q+1;/p-1

InChI key

AFIIOPIEVQSYHH-UHFFFAOYSA-M

Application

Used as an affinity alkylating agent for nicotinic receptors.


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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A K L Freitas et al.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas, 53(5), e9211-e9211 (2020-04-23)
Strenuous exercise triggers deleterious effects on the intestinal epithelium, but their mechanisms are still uncertain. Here, we investigated whether a prolonged training and an additional exhaustive training protocol alter intestinal permeability and the putative effect of alanyl-glutamine (AG) pretreatment in
Acetylcholinesterase hydrolysis of halogen substituted acetylcholines.
C Y Chiou et al.
Biochemical pharmacology, 17(5), 805-815 (1968-05-01)
S Tucek
The Journal of physiology, 322, 53-69 (1982-01-01)
1. The synthesis of acetylcholine (ACh) has been measured in homogenates of the sciatic nerve, normal and denervated extensor digitorum longus (e.d.l.) muscles, and central (innervated) and peripheral (non-innervated) parts of the diaphragm of the rat. The synthesis proceeded under



Global Trade Item Number

SKUGTIN
B121-500MG04061833258606