Diethyl(propyl)amine

Base Information

• Chemical Name: Diethyl(propyl)amine
• CAS No.: 4458-31-5
• Molecular Formula: C7H17N
• Molecular Weight: 115.219
• Hs Code.: 2921199090
• European Community (EC) Number: 224-710-7
• NSC Number: 1097
• UNII: G7TX2UQI1I
• DSSTox Substance ID: DTXSID70196227
• Nikkaji Number: J101.001H
• Wikidata: Q27160105
• Mol file: 4458-31-5.mol

Synonyms:4458-31-5;Diethyl(propyl)amine;N-(n-Propyl)diethylamine;N,N-diethylpropan-1-amine;Diethylpropylamine;N,N-Diethylpropylamine;N,N-Diethyl propanamine;1-Propanamine, N,N-diethyl-;N,N-Diethyl-1-propanamine;Diethyl-n-propylamine;N,N-Diethyl-n-propylamine;Propylamine, N,N-diethyl-;G7TX2UQI1I;Ethanamine, N-ethyl-N-propyl-;NSC-1097;EINECS 224-710-7;NSC1097;diethylpropyl amine;n-propyldiethylamine;3-diethylaminopropane;Propylamine,N-diethyl-;UNII-G7TX2UQI1I;1-Propanamine,N-diethyl-;SCHEMBL44445;n-Propanamine, N,N-diethyl-;N,N-Diethyl-1-propanamine #;CHEBI:88180;DTXSID70196227;(C2H5)2(n-C3H7)N;ADAL1186322;AMY13337;NSC 1097;AKOS006228510;FT-0629486;E79237;A905097;Q27160105

Chemical Property of Diethyl(propyl)amine

Chemical Property:

• Vapor Pressure: 17.3mmHg at 25°C
• Melting Point: -91.17°C (estimate)
• Refractive Index: 1.4064
• Boiling Point: 117.6°Cat760mmHg
• Flash Point: 12°C
• PSA: 3.24000
• Density: 0.761g/cm³
• LogP: 1.73820
• XLogP3: 2.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 115.136099547
• Heavy Atom Count: 8
• Complexity: 39.7

Purity/Quality:

99% ^*data from raw suppliers

N-(N-PROPYL)DIETHYLAMINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CCCN(CC)CC

Technology Process of Diethyl(propyl)amine

There total 19 articles about Diethyl(propyl)amine 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: 62.0%

N,N-diethylpropanamide (1114-51-8) → N,N-diethylpropylamine (4458-31-5)

Guidance literature:

With hydrogen; hexarhodium hexadecacarbonyl; decacarbonyldirhenium⁽⁰⁾; In 1,2-dimethoxyethane; at 160 ℃; for 36h; under 76000 Torr;

DOI:10.1016/S0040-4039(96)01458-X

Reference yield:

ethene (74-85-1) + carbon monoxide (201230-82-2) + diethylamine (109-89-7) → N,N-diethylpropylamine (4458-31-5) + 2-methyl-2-pentenal (14250-96-5,16958-22-8,623-36-9) + 3-hydroxyl-2-methylpentanal (615-30-5) + propionaldehyde (123-38-6)

Guidance literature:

With dicarbonylacetylacetonato rhodium (I); hydrogen; silica gel; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; 1-ethyl-3-methylimidazolium triflate; for 20h; under 7500.75 Torr; Reagent/catalyst; Catalytic behavior;

DOI:10.1002/anie.201301365

Reference yield:

ethene (74-85-1) + water (7732-18-5) + diethylamine (109-89-7) → N-formyldiethylamine (617-84-5) + N,N-diethylpropylamine (4458-31-5) + dipropylethylamine (20634-92-8) + triethylamine (121-44-8)

Guidance literature:

at 130 ℃; under 147102 Torr; Reagiert den Diaethylamin-formiat;

upstream raw materials:

triethylpropylammonium iodide

propyl bromide

ethylene glycol

diethylamine

Downstream raw materials:

heptafluoropropyl-bis-pentafluoroethyl-amine

triethylpropylammonium iodide

4'-N-N-diethylpropylamine-1'-[3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)]-semicarbazole

N-methyl-N,N-diethyl-n-propylammonium bis(fluorosulfonyl)imide

Refernces

• 1、 Tseng, Kuei-Nin T.,Kampf, Jeff W.,Szymczak, Nathaniel K.. "Modular Attachment of Appended Boron Lewis Acids to a Ruthenium Pincer Catalyst: Metal-Ligand Cooperativity Enables Selective Alkyne Hydrogenation". supporting information. p. 10378 - 10381. Retrieved 2016/09/04.
• 2、 Schneider, Martin Johannes,Lijewski, Martin,Woelfel, Rene,Haumann, Marco,Wasserscheid, Peter. "Continuous gas-phase hydroaminomethylation using supported ionic liquid phase catalysts". . p. 6996 - 6999. Retrieved 2013/07/26.