Triethylphenylammonium iodide

Base Information

• Chemical Name: Triethylphenylammonium iodide
• CAS No.: 1010-19-1
• Molecular Formula: C12H20 N . I
• Molecular Weight: 305.202
• Hs Code.: 29239000
• European Community (EC) Number: 213-774-1
• NSC Number: 97254
• UNII: R4F2JME3JH
• DSSTox Substance ID: DTXSID60883639
• Mol file: 1010-19-1.mol

Synonyms:triethylphenylamium;triethylphenylammonium;triethylphenylammonium benzenesulfonate;triethylphenylammonium chlorode;triethylphenylammonium hydroxide;triethylphenylammonium iodide

Chemical Property of Triethylphenylammonium iodide

Chemical Property:

• Melting Point: 127-133°C
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 0.00000
• Density: g/cm³
• LogP: 0.05760
• Sensitive.: Light Sensitive
• Water Solubility.: almost transparency
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 305.06405
• Heavy Atom Count: 14
• Complexity: 124

Purity/Quality:

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

Triethylphenylammonium Iodide ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi,T
• Statements: 36/37/38-23-22
• Safety Statements: 37/39-26-45

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of Triethylphenylammonium iodide

There total 1 articles about Triethylphenylammonium 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:

ethyl iodide (75-03-6) + N,N-diethylaniline (91-66-7) → N,N,N-triethylbenzenaminium iodide (1010-19-1)

Guidance literature:

at 100 ℃;

Reference yield:

N,N,N-triethylbenzenaminium iodide (1010-19-1) → ethanol (64-17-5) + hydrogen iodide (10034-85-2) + N,N-diethylaniline (91-66-7)

Guidance literature:

Reference yield:

ammonia (7664-41-7) + N,N,N-triethylbenzenaminium iodide (1010-19-1) → N,N-diethylaniline (91-66-7)

Guidance literature:

Electrolysis;

upstream raw materials:

ethyl iodide

N,N-diethylaniline

Downstream raw materials:

N,N-diethylaniline

ethanol

hydrogen iodide