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
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
Recommended Products
form
powder
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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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
Attila Rutai et al.
Shock (Augusta, Ga.), 54(1), 87-95 (2019-07-19)
The hypoxia-sensitive endothelin (ET) system plays an important role in circulatory regulation through vasoconstrictor ETA and ETB2 and vasodilator ETB1 receptors. Sepsis progression is associated with microcirculatory and mitochondrial disturbances along with tissue hypoxia. Our aim was to investigate the
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
Acetylcholinesterase hydrolysis of halogen substituted acetylcholines.
C Y Chiou et al.
Biochemical pharmacology, 17(5), 805-815 (1968-05-01)
Bromoacetylcholine as an affinity label of the acetylcholine receptor from Torpedo californica.
V N Damle et al.
Biochemical and biophysical research communications, 84(4), 845-851 (1978-10-30)
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