B121
Bromoacetylcholine bromide
Synonym(s):
2-(2-Bromoacetyloxy)-N.,N,N-trimethylethanaminium bromide
Sign Into View Organizational & Contract Pricing
Select a Size
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
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 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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Darlan Henrique Canei et al.
Veterinary world, 14(8), 2002-2008 (2021-09-28)
Urethral obstruction (UO) is a common condition in feline medicine. Severe acid-base and electrolyte disorders promote relevant electrocardiographic changes in these animals. Cardiac biomarkers such as cardiac troponin I have been shown to be useful in identifying cats with myocardial
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)
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
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