ACETYLCHOLINE CHLORIDE (60-31-1)

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Suppliers

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  5 mg
  $125.00

  10 mg
  $225.00

  25 mg
  $530.00

  50 mg
  $985.00

Most-cited Publications

• The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine. (Nature, 1980)
• Paradoxical Vasoconstriction Induced by Acetylcholine in Atherosclerotic Coronary Arteries (The New England Journal of Medicine, 1986)
• Atomic structure of acetylcholinesterase from Torpedo californica: a prototypic acetylcholine-binding protein (Science, 1991)
• Nicotinic acetylcholine receptor |[alpha]|7 subunit is an essential regulator of inflammation (Nature, 2002)
• THE REACTION OF ACETYLCHOLINE AND OTHER CARBOXYLIC ACID DERIVATIVES WITH HYDROXYLAMINE, AND ITS ANALYTICAL APPLICATION (Journal of Biological Chemistry, 1949)
• Refined Structure of the Nicotinic Acetylcholine Receptor at 4A Resolution (Journal of Molecular Biology, 2005)

Areas of Application

Safety

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Trends

Alternate Names

• Acetylcholine
• Miochol
• Acetylcholine Bromide
• Acetylcholine Iodide
• Acetylcholine Picrate
• Acetylcholine Fluoride
• Acetilcolina Cusi
• Acetylcholine Hydroxide
• Chloroacetylcholine
• Bromoacetylcholine
• Acetylcholine Picrate (1:1)
• 2-(Acetyloxy)-N,N,N-trimethylethanaminium
• Acetylcholine Perchlorate
• Acetylcholine Sulfate (1:1)
• Acetylcholine L-Tartrate
• Acetylcholine L Tartrate
• SMILES
  CC(=O)OCC[N+](C)(C)C.[Cl-]
• InChIKey
  JUGOREOARAHOCO-UHFFFAOYSA-M

External Links

• Pubchem - ACETYLCHOLINE CHLORIDE
• Wikipedia - acetylcholine chloride
  Acetylcholine (ACh) is an organic chemical that functions in the brain and body of many types of animals, including humans, as a neurotransmittera chemical released by nerve cells to send signals to other cells. Its name is derived from its chemical structure: it is an ester of acetic acid and choline. Parts in the body that use or are affected by acetylcholine are referred to as cholinergic.

Synthesis

Acetic Acid  +  Chlormequat (Ester from carboxilic acid(SN2))

ACETYL CHLORIDE  +  choline (O-acylation)

Reactant  +  dimethyl sulfide (Corey-Kim oxidation of secondary alcohols)

Synthesis of ACETYLCHOLINE CHLORIDE ›

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ACETYLCHOLINE CHLORIDE

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