Dinonylamine

Base Information

• Chemical Name: Dinonylamine
• CAS No.: 2044-21-5
• Molecular Formula: C18H39N
• Molecular Weight: 269.514
• Hs Code.: 2921199090
• European Community (EC) Number: 673-846-7
• NSC Number: 1764
• UNII: GVA41A9JG8
• DSSTox Substance ID: DTXSID50174386
• Nikkaji Number: J97.655E
• Wikidata: Q83044456
• Mol file: 2044-21-5.mol

Synonyms:Dinonylamine;2044-21-5;Dinonyl-amine;1-Nonanamine, N-nonyl-;di-n-nonylamine;N-nonylnonan-1-amine;GVA41A9JG8;NSC-1764;N-nonyl-1-Nonanamine;di(nonyl)-amine;1-Nonanamine, N-nonyl- (9CI);NSC 1764;Di(n-nonyl) amine;N,N-Dinonylamine #;1-Nonanamine,N-nonyl-;UNII-GVA41A9JG8;SCHEMBL64163;N,N-BIS(N-NONYL)AMINE;N-N-NONYL-N-NONYLAMINE;DTXSID50174386;NSC1764;MFHKEJIIHDNPQE-UHFFFAOYSA-N;BBL010307;MFCD00027338;STK371234;AKOS000508486;FS-5339;D2676;FT-0633994;19-IODO-5-CHOLESTEN-3BETA-OL3-ACETATE;T70537

Chemical Property of Dinonylamine

Chemical Property:

• Vapor Pressure: 0.000107mmHg at 25°C
• Melting Point: 24 °C
• Refractive Index: 1.445
• Boiling Point: 337.1 °C at 760 mmHg
• Flash Point: 145.9 °C
• PSA: 12.03000
• Density: 0.805 g/cm³
• LogP: 6.46810
• XLogP3: 7.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 16
• Exact Mass: 269.308250248
• Heavy Atom Count: 19
• Complexity: 129

Purity/Quality:

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

Dinonylamine ^*data from reagent suppliers

Safty Information:

• Statements: 34
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCNCCCCCCCCC
• Uses: Dinonylamine is an alkylamine that can be used in extraction of chloride complexes of niobium. A alkylamine that can be used in extraction of chloride complexes of niobium.

Technology Process of Dinonylamine

There total 4 articles about Dinonylamine 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:

nonanoic acid (112-05-0) → N-nonyl-nonanamide (114084-58-1) + n-Nonylamin (112-20-9) + di(n-nonyl)amine (2044-21-5)

Guidance literature:

With ammonia; water; hydrogen; [Ru₂(1,1,1-tris(diphenylphosphinomethyl)ethane)2Cl₃]Cl; In tetrahydrofuran; at 164 ℃; for 14h; under 30003 Torr;

DOI:10.1039/b706635j

Reference yield:

nonanoic acid (112-05-0) → N-nonyl-nonanamide (114084-58-1) + n-Nonylamin (112-20-9) + di(n-nonyl)amine (2044-21-5) + nonyl alcohol (143-08-8)

Guidance literature:

With ammonium hydroxide; hydrogen; [Ru₂(1,1,1-tris(diphenylphosphinomethyl)ethane)2Cl₃]Cl; In tetrahydrofuran; at 164 ℃; for 14h; under 30003 Torr;

DOI:10.1039/b706635j

Reference yield:

nonanoic acid (112-05-0) → n-Nonylamin (112-20-9) + di(n-nonyl)amine (2044-21-5) + nonyl alcohol (143-08-8)

Guidance literature:

With ammonium hydroxide; hydrogen; [Ru₂(1,1,1-tris(diphenylphosphinomethyl)ethane)2Cl₃]Cl; In tetrahydrofuran; at 164 ℃; for 14h; under 30003 Torr;

DOI:10.1039/b706635j

upstream raw materials:

N-methylaniline

nonanoic acid

Downstream raw materials:

N-methylaniline

3-(2,4-Dimethyl-phenyl)-1,1-dinonyl-urea

trinonyl-amine

Refernces

• 1、 Nú?ez Magro, Angel A.,Eastham, Graham R.,Cole-Hamilton, David J.. "The synthesis of amines by the homogeneous hydrogenation of secondary and primary amides". . p. 3154 - 3156. Retrieved 2008/02/13.