DECAMETHONIUM IODIDE

Base Information

• Chemical Name: DECAMETHONIUM IODIDE
• CAS No.: 1420-40-2
• Molecular Formula: C16H38 N2 . 2 I
• Molecular Weight: 512.3
• Hs Code.: 2923900090
• Mol file: 1420-40-2.mol

Synonyms:1,10-Decanediaminium,N,N,N,N',N',N'-hexamethyl-, diiodide (9CI); Ammonium, decamethylenebis[trimethyl-iodide] (6CI); Ammonium, decamethylenebis[trimethyl-, diiodide (8CI);Decamethylenebis(trimethylammonium) iodide (6CI); Decamethionium iodide;Decamethonium diiodide; Decamethonium iodide;Decamethylenebis(trimethylammonium) diiodide; Eulissin A; Eulixine; Procuran

Chemical Property of DECAMETHONIUM IODIDE

Chemical Property:

• Melting Point: 246-248 °C
• PSA: 0.00000
• LogP: -2.47240
• Water Solubility.: almost transparency

Purity/Quality:

98% ^*data from raw suppliers

Trimethyl-[10-(trimethylazaniumyl)decyl]azaniumDiiodide ^*data from reagent suppliers

Safty Information:

• Hazard Codes: T
• Statements: 25
• Safety Statements: 36/37/39-45

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Uses: Trimethyl-[10-(trimethylazaniumyl)decyl]azanium diiodide is a bisalkaloid derivative of a dicarboxylic acid, and is used as a reversible cholinesterase inhibitor.

Technology Process of DECAMETHONIUM IODIDE

There total 2 articles about DECAMETHONIUM 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: 82.0%

diaminodecane (646-25-3) + methyl iodide (74-88-4) → N,N,N,N',N',N'-hexamethyldecanediammonium iodide (1420-40-2)

Guidance literature:

With 1,2,2,6,6-pentamethylpiperidine; In N,N-dimethyl-formamide; at 20 ℃;

DOI:10.1002/chem.202002264

Reference yield:

1,10-diiododecane (16355-92-3) + trimethylamine (75-50-3) → N,N,N,N',N',N'-hexamethyldecanediammonium iodide (1420-40-2)

Guidance literature:

With ethanol;

Reference yield:

1,3-Diiodobenzene (626-00-6) + N,N,N,N',N',N'-hexamethyldecanediammonium iodide (1420-40-2) → C6H4I2*2I(1-)*C16H38N2(2+)

Guidance literature:

In methanol; chloroform; at 20 ℃; regioselective reaction;

DOI:10.1002/chem.202002264

upstream raw materials:

1,10-diiododecane

trimethylamine

diaminodecane

methyl iodide

Refernces