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Merck
CN

B121

Sigma-Aldrich

Bromoacetylcholine bromide

别名:

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

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About This Item

经验公式(希尔记法):
C7H15BrNO2 · Br
CAS号:
分子量:
305.01
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

表单

powder

溶解性

H2O: soluble

储存温度

−20°C

SMILES字符串

[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

应用

Used as an affinity alkylating agent for nicotinic receptors.

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

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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)
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
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
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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