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(+/-)-Muscarine chloride

Base Information
  • Chemical Name:(+/-)-Muscarine chloride
  • CAS No.:2936-25-6
  • Molecular Formula:C9H20NO2*Cl
  • Molecular Weight:209.716
  • Hs Code.:
  • European Community (EC) Number:636-708-7
  • ChEMBL ID:CHEMBL1871893
  • DSSTox Substance ID:DTXSID701018053
  • Mol file:2936-25-6.mol
(+/-)-Muscarine chloride

Synonyms:(+/-)-Muscarine chloride;(+/-)-Muscarine chloride hydrate;2936-25-6;(4-hydroxy-5-methyloxolan-2-yl)methyl-trimethylazanium;chloride;ribo-Hexitol, 2,5-anhydro-1,3,6-trideoxy-1-(trimethylammonio)-, chloride;MLS002153170;CHEMBL1871893;DTXSID701018053;HMS2235F18;HMS3372G09;MFCD00055067;AKOS030241231;Tetrahydro-4-hydroxy-N,N,N,5-tetramethyl-2-furanmethanammonium chloride hydrate;SMR001230663;(+/-)-Muscarine chloride hydrate, >=98% (HPLC);J-017483;Trimethyl(tetrahydro-4-hydroxy-5-methylfurfuryl)ammonium chloride;93457-82-0

Suppliers and Price of (+/-)-Muscarine chloride
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • (+/-)-MuscarineChloride
  • 25mg
  • $ 1175.00
  • Sigma-Aldrich
  • (±)-Muscarine chloride hydrate ≥98% (HPLC)
  • 25mg
  • $ 562.00
  • Sigma-Aldrich
  • (±)-Muscarine chloride hydrate ≥98% (HPLC)
  • 5mg
  • $ 140.00
  • American Custom Chemicals Corporation
  • (+/-)-MUSCARINE CHLORIDE 95.00%
  • 10MG
  • $ 883.49
  • American Custom Chemicals Corporation
  • (+/-)-MUSCARINE CHLORIDE 95.00%
  • 5MG
  • $ 578.00
Total 10 raw suppliers
Chemical Property of (+/-)-Muscarine chloride
Chemical Property:
  • Melting Point:180-181oC 
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:29.46000 
  • Density:g/cm3 
  • LogP:-2.76510 
  • Storage Temp.:room temp 
  • Solubility.:deionized water: ≥20mg/mL 
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:209.1182566
  • Heavy Atom Count:13
  • Complexity:153
Purity/Quality:

98%,99%, *data from raw suppliers

(+/-)-MuscarineChloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xn 
  • Statements: 22-36 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CC1C(CC(O1)C[N+](C)(C)C)O.[Cl-]
  • Description Muscarine is a natural alkaloid that is found in a number of wild mushrooms. Despite the fact that muscarine does not have any therapeutic value, it is of interest because of its expressed toxic properties, which made it one of the first systematically studied cholinomimetic substances. (+/-)-MUSCARINE CHLORIDE was an underlying classification of cholinergic muscarinic receptors. The action of muscarine is similar to that of acetylcholine on peripheral autonomic effector organs, and atropine is an antagonist to it. Unlike acetylcholine, muscarine does not act on nicotinic receptors.
  • Uses (+/-)-Muscarine Chloride is a muscarinic acteylcholine receptor agonist.
Technology Process of (+/-)-Muscarine chloride

There total 20 articles about (+/-)-Muscarine chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 7 steps
1: 90 percent / CrO3*2C5H5N / CH2Cl2
2: 97 percent / benzene / 3 h / 25 °C
3: 93 percent / Et3N / CH2Cl2
4: 81 percent / H2 / 10percent Pd/C / various solvent(s)
5: LiAlH4 / diethyl ether / 1 h / Heating
7: AgCl / H2O
With lithium aluminium tetrahydride; hydrogen; dipyridine chromium trioxide; triethylamine; silver(I) chloride; palladium on activated charcoal; In diethyl ether; dichloromethane; water; benzene;
DOI:10.1021/jo01304a056
Guidance literature:
Multi-step reaction with 6 steps
1: 97 percent / benzene / 3 h / 25 °C
2: 93 percent / Et3N / CH2Cl2
3: 81 percent / H2 / 10percent Pd/C / various solvent(s)
4: LiAlH4 / diethyl ether / 1 h / Heating
6: AgCl / H2O
With lithium aluminium tetrahydride; hydrogen; triethylamine; silver(I) chloride; palladium on activated charcoal; In diethyl ether; dichloromethane; water; benzene;
DOI:10.1021/jo01304a056
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