Diheptylamine

Base Information

• Chemical Name: Diheptylamine
• CAS No.: 2470-68-0
• Molecular Formula: C14H31 N
• Molecular Weight: 213.407
• Hs Code.: 2921199090
• European Community (EC) Number: 679-968-7
• NSC Number: 79264
• UNII: 5E36MJ5OI8
• DSSTox Substance ID: DTXSID8062444
• Nikkaji Number: J80.497E
• Wikidata: Q26841313
• Mol file: 2470-68-0.mol

Synonyms:Diheptylamine;2470-68-0;N-heptylheptan-1-amine;Di-n-heptylamine;1-Heptanamine, N-heptyl-;5E36MJ5OI8;NSC 79264;NSC-79264;AI3-16572;N,N-Diheptylamine #;UNII-5E36MJ5OI8;SCHEMBL36300;N-HEPTYL-1-HEPTANAMINE;DTXSID8062444;NSC79264;BBL009739;MFCD00027309;STL145786;AKOS005174422;NCGC00341246-01;VS-02162;CS-0187367;D2675;FT-0634305;EN300-40587;F17086;AB00982877-01;AB00982877-03;Q26841313

Chemical Property of Diheptylamine

Chemical Property:

• Vapor Pressure: 0.00528mmHg at 25°C
• Melting Point: 1°C
• Refractive Index: 1.4370-1.4410
• Boiling Point: 274.8°Cat760mmHg
• PKA: 11.33±0.19(Predicted)
• Flash Point: 107.9°C
• PSA: 12.03000
• Density: 0.794g/cm³
• LogP: 4.90770
• XLogP3: 5.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 12
• Exact Mass: 213.245649993
• Heavy Atom Count: 15
• Complexity: 89.5

Purity/Quality:

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

Diheptylamine >98.0%(GC)(T) ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCNCCCCCCC
• Uses: Diheptylamine is used in organic syntheses.

Technology Process of Diheptylamine

There total 24 articles about Diheptylamine 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:

1,4-dioxane (123-91-1,28347-88-8,28347-91-3,39449-24-6,54841-74-6) + N-phenethyl-heptanamide (251350-20-6) → diheptylamine (2470-68-0) + 1-Heptylamine (111-68-2) + heptyl-phenethyl-amine (637359-02-5) + phenethylamine (64-04-0)

Guidance literature:

at 250 ℃; under 147102 - 220652 Torr; Produkt₅:Aethylbenzol_.Hydrogenation;

DOI:10.1021/ja01326a061

Reference yield:

→ diheptylamine (2470-68-0) + 1-Heptylamine (111-68-2)

Guidance literature:

With 1,4-dioxane; copper chromite; at 250 ℃; under 147102 - 220652 Torr; Hydrogenation;

Reference yield:

1-heptanal oxime (629-31-2) → diheptylamine (2470-68-0) + 1-Heptylamine (111-68-2)

Guidance literature:

With diethyl ether; nickel kieselguhr; at 100 - 125 ℃; under 73550.8 - 110326 Torr; Hydrogenation;

DOI:10.1021/ja01332a043

upstream raw materials:

1-Bromoheptane

1-heptanal oxime

1-amino-heptan-1-ol

heptyl heptanoate

Downstream raw materials:

tri-n-heptylamine

diheptyl-nitro-amine

2-Diheptylaminomethyl-phenol

1,1-di-(n-heptyl)-3-(2,4-dimethylphenyl)urea

Refernces

• 1、 Rao, H. Surya Prakash,Bharathi. "Reduction of oximes with sodium borohydride - Copper (II) sulfate in methanol". . p. 1072 - 1074. Retrieved 2007/10/03.