Diethylammonium iodide

Base Information

• Chemical Name: Diethylammonium iodide
• CAS No.: 19833-78-4
• Molecular Formula: C4H11 N . H I
• Molecular Weight: 201.05
• Hs Code.: 29211990
• European Community (EC) Number: 243-358-5
• Mol file: 19833-78-4.mol

Synonyms:Diethylammonium iodide;diethylazanium;iodide;diethylazanium iodide;EINECS 243-358-5;C4H11N.HI;C4-H11-N.H-I;Diathylammoniumjodid;SCHEMBL566921;Diethylamine Hydroiodide, >/=97%

Chemical Property of Diethylammonium iodide

Chemical Property:

• Vapor Pressure: 218mmHg at 25°C
• Melting Point: 173.0 to 177.0 °C
• Boiling Point: 57.3°Cat760mmHg
• Flash Point: °C
• PSA: 12.03000
• Density: g/cm³
• LogP: 2.00490
• Water Solubility.: Soluble in water
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 201.00145
• Heavy Atom Count: 6
• Complexity: 11.1

Purity/Quality:

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

Diethylamine Hydroiodide >97.0%(N)(T) ^*data from reagent suppliers

Safty Information:

• Statements: 22-36/37/38
• Safety Statements: 36-44

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC[NH2+]CC.[I-]
• Uses: The iodide and bromide based alkylated halides find applications as precursors for fabrication of perovskites for photovoltaic applications.

Technology Process of Diethylammonium iodide

There total 11 articles about Diethylammonium 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: 87.1%

heptafluoropropyl-diiodo-phosphine (678-07-9) + diethylamine (109-89-7) → Diethylamino-iod-heptafluorpropyl-phosphin (21941-42-4) + di-ethylamine hydroiodide (19833-78-4)

Guidance literature:

In hexane; under Ar; warming up from -40°C to 20°C;

Reference yield: 75.6%

trifluoromethyldiiodophosphine (421-59-0) + diethylamine (109-89-7) → Diethylamino-iod-trifluormethyl-phosphin (21941-41-3) + di-ethylamine hydroiodide (19833-78-4)

Guidance literature:

In hexane; under Ar; warming up from -40°C to 20°C;

Reference yield: 63.2%

diethylamine (109-89-7) + iododiphenylphosphine oxide (92587-60-5) → N,N-diethyl P,P-diphenylphosphinamide (56372-47-5) + di-ethylamine hydroiodide (19833-78-4)

Guidance literature:

In dichloromethane;

upstream raw materials:

diethyl ether

bis-(diethylamino)methane

ethyl iodide

Cyclohexyl iodide

Refernces