Tiametonium iodide

Base Information

• Chemical Name: Tiametonium iodide
• CAS No.: 10433-71-3
• Molecular Formula: C₁₂H₃₀N₂S*2I
• Molecular Weight: 488.259
• Hs Code.: 2930909090
• UNII: Z0OMD60978
• DSSTox Substance ID: DTXSID40883137
• Wikidata: Q27294845
• NCI Thesaurus Code: C76614
• ChEMBL ID: CHEMBL2105381
• Mol file: 10433-71-3.mol

Synonyms:Tiametonium iodide;10433-71-3;Tiametonium iodide [INN];Tiametonii iodidum;Iodure de tiametonium [INN-French];Ioduro de tiametonio;Iodure de tiametonium;Tiametonii iodidum [INN-Latin];Ioduro de tiametonio [INN-Spanish];UNII-Z0OMD60978;Thiodiethylenebis(ethyldimethylammonium iodide);(Thiodiethylene)bis(ethyldimethylammonium iodide);Z0OMD60978;Ethanaminium, 2,2'-thiobis(N-ethyl-N,N-dimethyl-, diiodide;ethyl-[2-[2-[ethyl(dimethyl)azaniumyl]ethylsulfanyl]ethyl]-dimethylazanium;diiodide;AMMONIUM, THIODIETHYLENEBIS(ETHYLDIMETHYL-, DIIODIDE;Ethanaminium, 2,2'-thiobis[N-ethyl-N,N-dimethyl-, diiodide;tiametoniumiodid;Tiametoniumiodide;SCHEMBL2733793;CHEMBL2105381;C12H30I2N2S;DTXSID40883137;AKOS024427529;ethyl-[2-[2-[ethyl(dimethyl)azaniumyl]ethylsulfanyl]ethyl]-dimethylazanium diiodide;LS-19085;Ammonium, (thiodiethylene)bis[ethyldimethyl-, diiodide;Q27294845

Chemical Property of Tiametonium iodide

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 25.30000
• Density: g/cm³
• LogP: -4.07980
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 8
• Exact Mass: 488.02192
• Heavy Atom Count: 17
• Complexity: 149

Purity/Quality:

98%,99%, ^*data from raw suppliers

ETHYL[2-((2-[ETHYL(DIMETHYL)AMMONIO]ETHYL)SULFANYL)ETHYL]DIMETHYLAMMONIUM DIIODIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC[N+](C)(C)CCSCC[N+](C)(C)CC.[I-].[I-]

Technology Process of Tiametonium iodide

There total 1 articles about Tiametonium iodide 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:

Reference yield:

2,2'-sulfurbis(N,N-dimethylethan-1-amine) (3018-41-5) + ethyl iodide (75-03-6) → N,N'-diethyl-N,N,N',N'-tetramethyl-N,N'-(3-thia-pentanediyl)-di-ammonium; diiodide (10433-71-3)

Guidance literature:

upstream raw materials:

2,2'-sulfurbis(N,N-dimethylethan-1-amine)

ethyl iodide