70623-44-8

Basic information

• Product Name: Acetylcholine chloride
• Synonyms: Acetilcolina cloruro;Acetilcolina cloruro [dcit]
• CAS NO: 70623-44-8
• Molecular Formula: C7H16ClNO2
• Molecular Weight: 181.66044
• Mol File: 70623-44-8.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Acetylcholine chloride(CAS DataBase Reference)
• NIST Chemistry Reference: Acetylcholine chloride(70623-44-8)
• EPA Substance Registry System: Acetylcholine chloride(70623-44-8)

Safety Data

• Hazardous Substances Data: 70623-44-8(Hazardous Substances Data)

Upstream product

• 67-48-1 choline chloride 
• 64-19-7 acetic acid 
• 852998-99-3 C₇H₁₆NO₂⁽¹⁺⁾*C₂₈H₃₂N₄O₅*Cl^(1-) 
• 75-50-3 trimethylamine 
• 75-36-5 acetyl chloride 
• 108-24-7 acetic anhydride 

Downstream Products

• 1095097-66-7 4-(4-aminophenylazo)naphthalen-1-amine 

Relevant articles and documents

Catalytic application of zinc complex of oxygen depleted 1,3-bis(pyrazole)-p-tert-butylcalix[4]arene

In this paper we have described the synthesis and coordination properties of monometallic Zinc complex of oxygen depleted bis(pyrazole)-p-tert-butylcalix[4]arene ligand. We also present the catalytic activity of the Zinc–bis(pyrazole) complex, in acetylation of alcohols and lactide polymerization.

Cavitand templated catalysis of acetylcholine

A Zn-salen-modified cavitand templates the catalytic formation of acetylcholine from choline and acetic anhydride. The Royal Society of Chemistry 2006.

Recognition of quaternary ammonium salts with tetrapeptides containing α-aminoisobutyric acid as a conformational constraint

Tetrapeptides Trp-Aib-Gly-Leu-NH-Ar (Aib:α-aminoisobutyric acid, 2-amino-2-methylpropanoic acid, Ar = phenyl or 3,5-dimethylphenyl) were synthesized. The peptides bound quaternary ammonium salts as guests in CDCl3. For every guest, the binding constant K of the peptide host which has a 3,5-dimethylphenyl group was larger than that of the host which has a phenyl group. ROESY analysis of the complex revealed that the N+-CH3 groups of the guests were close to the aromatic moieties of the host in the complex. The charge in cation guests, the φ-basicity of the host, and the turn conformation of the peptides were important factors for the complexation.