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Acetylcholine bromide

Acetylcholine bromide structure

Acetylcholine bromide 

structure
  • CAS No:

    66-23-9

  • Formula:

    C7H16NO2.Br

  • Chemical Name:

    Acetylcholine bromide

  • Synonyms:

    Ethanaminium,2-(acetyloxy)-N,N,N-trimethyl-,bromide (1:1);Choline acetate (ester),bromide;Ethanaminium,2-(acetyloxy)-N,N,N-trimethyl-,bromide;Choline,acetyl-,bromide;Acetylcholine bromide;Pragmoline;Tonocholin B;Acetylcholine bromhydrate;N,N,N-Trimethyl-2-acetoxyethylammonium bromide;Acetylcholine hydrobromide;Trimethyl(2-acetoxyethyl)ammonium bromide;(2-Acetyloxyethyl)trimethylammonium bromide;[2-(Acetyloxy)ethyl]trimethylazanium bromide

  • Categories:

    Organic Chemistry  >  Amides

Description

WHITE TO LIGHT BEIGE ADHERING CRYSTALLINE SOLID


Acetylcholine bromide is the bromide salt of acetylcholine. It is a quaternary ammonium salt and a bromide salt. It contains an acetylcholine.|A neurotransmitter found at neuromuscular junctions, autonomic ganglia, parasympathetic effector junctions, a subset of sympathetic effector junctions, and at many sites in the central nervous system.

Acetylcholine bromide Basic Attributes

226.11

225.036438

3572117

200-622-4

C12HG588IF

4678

29379000

Characteristics

26.3

-2.74030

White powder

1.4246 (rough estimate)

146 °C

H2O: almost transparency

−20°C

Safety Information

NONH for all modes of transport

3

36/37/38

26-36-37/39

FZ9680000

Xi

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 39 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

Drugs used to cause dilation of the blood vessels. (See all compounds classified as Vasodilator Agents.)|Drugs that bind to and activate cholinergic receptors. (See all compounds classified as Cholinergic Agonists.)

2-(Acetyloxy)-N,N,N-trimethylethanaminium

Acetylcholine bromide Use and Manufacturing

Methods of Manufacturing

Pass ethylene oxide gas into trimethylamine and react to obtain trimethylamine ethanol, which is brominated with hydrobromic acid, acylated with acetic anhydride, and finally recrystallized from ethanol to obtain this product.

Uses

For biochemical research, etc.

Ethanaminium, 2-(acetyloxy)-N,N,N-trimethyl-, bromide (1:1): ACTIVE

Computed Properties

Molecular Weight:226.11
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:225.03644
Monoisotopic Mass:225.03644
Topological Polar Surface Area:26.3
Heavy Atom Count:11
Complexity:115
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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