4-Aminophenyltrimethylammonium iodide

Base Information

• Chemical Name: 4-Aminophenyltrimethylammonium iodide
• CAS No.: 18953-50-9
• Molecular Formula: C9H15N2+
• Molecular Weight: 151.2283
• NSC Number: 86674
• DSSTox Substance ID: DTXSID90940466
• Mol file: 18953-50-9.mol

Synonyms:4-Aminophenyltrimethylammonium iodide;Trimethylammoniumaniline iodide;18953-50-9;NSC 86674;(p-Aminophenyl)trimethylammonium iodide;(4-aminophenyl)-trimethylazanium;iodide;4-Amino-N,N,N-trimethylbenzenaminium iodide;Benzenaminium, 4-amino-N,N,N-trimethyl-, iodide;AMMONIUM, (p-AMINOPHENYL)TRIMETHYL-, IODIDE;SCHEMBL3384179;C9H15N2.I;DTXSID90940466;CCG-2154;NSC86674;NSC-86674;LS-16710;4-AMINO-N,N,N-TRIMETHYLANILINIUM IODIDE

Chemical Property of 4-Aminophenyltrimethylammonium iodide

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: g/cm³
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 278.02800
• Heavy Atom Count: 12
• Complexity: 118

Purity/Quality:

98% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

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

Technology Process of 4-Aminophenyltrimethylammonium iodide

There total 5 articles about 4-Aminophenyltrimethylammonium 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: 69.0%

4-(1,3-dioxoisoindolin-2-yl)-N,N,N-trimethylbenzenaminium iodide (1522059-57-9) → 4-amino-N,N,N-trimethylbenzene ammonium iodide (18953-50-9)

Guidance literature:

With hydrazine hydrate; In ethanol; at 20 ℃; for 24h;

DOI:10.1039/c3cc47056c

Reference yield:

N-(4-(dimethylamino)phenyl)formamide (18606-63-8) + methyl iodide (74-88-4) → 4-amino-N,N,N-trimethylbenzene ammonium iodide (18953-50-9)

Guidance literature:

With methanol; at 100 ℃;

Reference yield:

4-amino-N,N-dimethylaniline (99-98-9) → 4-amino-N,N,N-trimethylbenzene ammonium iodide (18953-50-9)

Guidance literature:

Multi-step reaction with 3 steps

1: triethylamine / toluene / 130 °C / Dean-Stark

2: chloroform / 24 h / 50 °C

3: hydrazine hydrate / ethanol / 24 h / 20 °C

With hydrazine hydrate; triethylamine; In ethanol; chloroform; toluene;

DOI:10.1039/c3cc47056c

upstream raw materials:

N-(4-(dimethylamino)phenyl)formamide

methyl iodide

N'-acetyl-N,N-dimethyl-1,4-phenylenediamine

N'-benzylidene-N,N-dimethyl-p-phenylenediamine

Downstream raw materials:

{4-[3-(2-Chloro-ethylsulfanyl)-propionylamino]-phenyl}-trimethyl-ammonium; iodide