N-Ethyloctylamine

Base Information

• Chemical Name: N-Ethyloctylamine
• CAS No.: 4088-36-2
• Molecular Formula: C10H23 N
• Molecular Weight: 157.2963
• Hs Code.: 2921199090
• UNII: I381LB1W1O
• DSSTox Substance ID: DTXSID30193858
• Nikkaji Number: J57.822C
• Wikidata: Q27280308
• Mol file: 4088-36-2.mol

Synonyms:N-Ethyloctylamine;4088-36-2;Ethyloctylamine;N-ethyloctan-1-amine;1-Octanamine, N-ethyl-;N-ethyl-1-octanamine;UNII-I381LB1W1O;I381LB1W1O;ethyloctyl-amine;ethyl-n-octylamine;?N-Ethyloctylamine;SCHEMBL37551;OCTYLAMINE, N-ETHYL-;DTXSID30193858;AKOS005296683;FT-0750559;Q27280308

Chemical Property of N-Ethyloctylamine

Chemical Property:

• Vapor Pressure: 0.185mmHg at 25°C
• Melting Point: -38.5°C (estimate)
• Refractive Index: 1.4286
• Boiling Point: 211.2 °C at 760 mmHg
• PKA: 10.93±0.19(Predicted)
• Flash Point: 81.8 °C
• PSA: 26.02000
• Density: 0.795 g/cm³
• LogP: 3.78450
• XLogP3: 3.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 8
• Exact Mass: 157.183049738
• Heavy Atom Count: 11
• Complexity: 61.9

Purity/Quality:

98%min ^*data from raw suppliers

ETHYL(OCTYL)AMINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCNCC

Technology Process of N-Ethyloctylamine

There total 6 articles about N-Ethyloctylamine 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: 90.0%

triethyl borane (97-94-9) + N-chloro-1-octylamine (89231-76-5) → ethyl-n-octylamine (4088-36-2)

Guidance literature:

With sodium hydrogencarbonate; In tetrahydrofuran; at 0 ℃; for 0.0833333h;

DOI:10.1021/jo00183a035

Reference yield:

N-octylacetamide (7462-62-6) → ethyl-n-octylamine (4088-36-2)

Guidance literature:

With phenylsilane-d3; C₃₆H₄₈F₆N₆NiO₅S₂; In toluene; at 110 ℃; for 24h; Inert atmosphere; Schlenk technique;

DOI:10.1039/d1cc03537a

Reference yield:

n-Octylamine (111-86-4) → ethyl-n-octylamine (4088-36-2)

Guidance literature:

Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 2 h / 20 °C

2: C₃₆H₄₈F₆N₆NiO₅S₂; phenylsilane-d3 / toluene / 24 h / 110 °C / Inert atmosphere; Schlenk technique

With phenylsilane-d3; C₃₆H₄₈F₆N₆NiO₅S₂; triethylamine; In dichloromethane; toluene;

DOI:10.1039/d1cc03537a

upstream raw materials:

N-ethyl-N-octyl-toluene-4-sulfonamide

triethyl borane

N-chloro-1-octylamine

n-Octylamine

Refernces

• 1、 Klamann,Hofbauer. "-". . p. 62,75. Retrieved 1953.