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:
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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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
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
Acetylcholinesterase hydrolysis of halogen substituted acetylcholines.
C Y Chiou et al.
Biochemical pharmacology, 17(5), 805-815 (1968-05-01)