AMMONIUM, (p-(TRIMETHYLAMMONIO)PHENETHYL)TRIMETHYL-, DIIODIDE

Base Information

• Chemical Name: AMMONIUM, (p-(TRIMETHYLAMMONIO)PHENETHYL)TRIMETHYL-, DIIODIDE
• CAS No.: 27389-67-9
• Molecular Formula: C14H26 N2 . 2 I
• Molecular Weight: 476.183
• DSSTox Substance ID: DTXSID00950076
• Mol file: 27389-67-9.mol

Synonyms:27389-67-9;Phenyldimethonium iodide;AMMONIUM, (p-(TRIMETHYLAMMONIO)PHENETHYL)TRIMETHYL-, DIIODIDE;(p-(Trimethylammonio)phenethyl)trimethylammonium diiodide;M & B 1950;M&B-1950;Dimethojodid 2-(p-dimethylaminofenyl)-ethyl-dimethylaminu [Czech];Dimethojodid 2-(p-dimethylaminofenyl)-ethyl-dimethylaminu;DTXSID00950076;C14H26N2.2I;AKOS040750477;C14-H26-N2.2I;LS-19127;Ammonium, (ethylene-p-phenylene)bis[trimethyl-, diiodide;N,N,N-Trimethyl-4-[2-(trimethylazaniumyl)ethyl]anilinium diiodide;trimethyl-[4-[2-(trimethylazaniumyl)ethyl]phenyl]azanium;diiodide;Benzenaminium, 4,4'-(1,2-ethanediyl)bis[N,N,N-trimethyl-, diiodide

Chemical Property of AMMONIUM, (p-(TRIMETHYLAMMONIO)PHENETHYL)TRIMETHYL-, DIIODIDE

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: g/cm³
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 476.01854
• Heavy Atom Count: 18
• Complexity: 202

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C[N+](C)(C)CCC1=CC=C(C=C1)[N+](C)(C)C.[I-].[I-]

Technology Process of AMMONIUM, (p-(TRIMETHYLAMMONIO)PHENETHYL)TRIMETHYL-, DIIODIDE

There total 3 articles about AMMONIUM, (p-(TRIMETHYLAMMONIO)PHENETHYL)TRIMETHYL-, DIIODIDE 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:

p-Aminophenethylamine (13472-00-9) + methyl iodide (74-88-4) → trimethyl-(4-trimethylammonio-phenethyl)-ammonium; diiodide (27389-67-9)

Guidance literature:

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

DOI:10.1021/jo00805a021

Reference yield:

(4-dimethylamino-phenyl)-acetonitrile (34906-70-2) → trimethyl-(4-trimethylammonio-phenethyl)-ammonium; diiodide (27389-67-9)

Guidance literature:

Multi-step reaction with 2 steps

1: sodium; alcohol

2: alkali

With ethanol; sodium;

Reference yield:

4-Dimethylaminophenethylamine (52632-05-0) + methyl iodide (74-88-4) → trimethyl-(4-trimethylammonio-phenethyl)-ammonium; diiodide (27389-67-9)

Guidance literature:

With alkali;

upstream raw materials:

4-Dimethylaminophenethylamine

methyl iodide

p-Aminophenethylamine

(4-dimethylamino-phenyl)-acetonitrile

Downstream raw materials:

N,N-dimethy-4-vinylaniline