N-Ethylpentylamine

Base Information

• Chemical Name: N-Ethylpentylamine
• CAS No.: 17839-26-8
• Molecular Formula: C7H17 N
• Molecular Weight: 115.219
• Hs Code.: 2921199090
• DSSTox Substance ID: DTXSID60338139
• Nikkaji Number: J99.926A
• Wikidata: Q82106354
• Mol file: 17839-26-8.mol

Synonyms:N-Ethylpentylamine;17839-26-8;N-ethylpentan-1-amine;1-Pentanamine, N-ethyl-;N-Ethyl-Pentylamine;Pentylamine, N-ethyl-;ethylpentylamine;Aethyl- (Amyl)amin;ethyl ((pentyl)amine;N-Ethyl-n-pentylamine #;SCHEMBL56918;DTXSID60338139;AKOS000154309;FT-0693360

Chemical Property of N-Ethylpentylamine

Chemical Property:

• Vapor Pressure: 5.71mmHg at 25°C
• Melting Point: -38°C (estimate)
• Refractive Index: 1.4122
• Boiling Point: 142°C at 760 mmHg
• Flash Point: 26.8°C
• PSA: 12.03000
• Density: 0.753g/cm³
• LogP: 2.17700
• XLogP3: 2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 115.136099547
• Heavy Atom Count: 8
• Complexity: 35.4

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCNCC

Technology Process of N-Ethylpentylamine

There total 9 articles about N-Ethylpentylamine 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:

ethyl-benzyl-pentyl-amine (855271-19-1) → N-n-pentyl-N-ethylamine (17839-26-8)

Guidance literature:

With acetic acid; platinum; at 65 - 75 ℃; under 2206.5 Torr; durch Hydrogenolyse;

Reference yield:

ethanol (64-17-5) + n-Pentylamine (110-58-7) → N-n-pentyl-N-ethylamine (17839-26-8)

Guidance literature:

With copper chromite; diethyl ether; at 180 ℃; under 91938.4 Torr; unter Wasserstoff-Druck;

DOI:10.1021/ja01267a081

Reference yield:

N-benzyl-N-pentylamine (25468-43-3) → N-n-pentyl-N-ethylamine (17839-26-8)

Guidance literature:

Multi-step reaction with 2 steps

1: ethanol

2: platinum; glacial acetic acid / 65 - 75 °C / 2206.5 Torr / durch Hydrogenolyse

With ethanol; acetic acid; platinum;

upstream raw materials:

ethyl-benzyl-pentyl-amine

ethanol

n-Pentylamine

pentanonitrile

Downstream raw materials:

2-(ethyl-pentyl-amino)-ethanol

S-benzyl ethyl-n-pentylthiolcarbamate

Refernces

• 1、 -. "Preparation process of aminoacetamide derivative". . . Retrieved 2008/06/13.