1-Pentanamine, N-butyl-

Base Information

• Chemical Name: 1-Pentanamine, N-butyl-
• CAS No.: 39536-61-3
• Molecular Formula: C9H21 N
• Molecular Weight: 143.272
• Hs Code.: 2921199090
• European Community (EC) Number: 254-497-6
• DSSTox Substance ID: DTXSID7068180
• Nikkaji Number: J261.379D
• Wikidata: Q81994891
• Mol file: 39536-61-3.mol

Synonyms:N-Amyl-N-butylamine;39536-61-3;1-Pentanamine, N-butyl-;N-butylpentan-1-amine;N-Amylbutylamine;N-Butylpentylamine;n-Amyl-n-butyl amine;N-(n-Amyl)-n-butylamine;EINECS 254-497-6;butyl(pentyl)amine;butyl-pentyl-amine;N-Butyl-1-pentanamine;n-Butyl-n-pentylamine #;SCHEMBL166121;DTXSID7068180;MFCD00048837;AKOS000231756;FT-0693707

Chemical Property of 1-Pentanamine, N-butyl-

Chemical Property:

• Vapor Pressure: 0.653mmHg at 25°C
• Boiling Point: 186.7°Cat760mmHg
• Flash Point: 54.1°C
• PSA: 12.03000
• Density: 0.77g/cm³
• LogP: 2.95720
• XLogP3: 3.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 7
• Exact Mass: 143.167399674
• Heavy Atom Count: 10
• Complexity: 52.7

Purity/Quality:

99% ^*data from raw suppliers

N-AMYL-N-BUTYLAMINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCNCCCC

Technology Process of 1-Pentanamine, N-butyl-

There total 23 articles about 1-Pentanamine, N-butyl- 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: 97.0%

propyl cyanide (109-74-0) + n-Pentylamine (110-58-7) → N-butylpentylamine (39536-61-3)

Guidance literature:

With 3 % platinum on carbon; hydrogen; In toluene; at 105 ℃; under 4500.45 Torr; Flow reactor;

DOI:10.1039/c2cy20431b

Reference yield: 80.0%

N-(2-bromoprop-2-enyl)-N-butylamine (89796-20-3) + benzaldehyde (100-52-7) → N-butylpentylamine (39536-61-3) + 1,4-diphenyl-but-2-yne-1,4-diol (4482-17-1)

Guidance literature:

With n-butyllithium; water; Yield given. Multistep reaction; 1) Et₂O, hexane, 20 deg C, 30 min, 2) Et₂O, hexane, 20 deg C, 12 h, 3) Et₂O, hexane;

DOI:10.1021/jo960025+

Reference yield: 72.0%

propyl cyanide (109-74-0) + n-Pentylamine (110-58-7) → N-butylpentylamine (39536-61-3) + dibutylamine (111-92-2)

Guidance literature:

With 3 % platinum on carbon; hydrogen; In toluene; at 105 ℃; under 4500.45 Torr; Flow reactor;

DOI:10.1039/c2cy20431b

upstream raw materials:

N-n-butyl-N-n-pentylbenzylamine

pentanal

N-butylamine

1-Bromopentane

Refernces

• 1、 Barluenga, Jose,Canteli, Rosa-Maria,Florez, Josefa. "Novel cleavage of propargylamines by reaction with organolithium compounds". . p. 3646 - 3649. Retrieved 2007/10/03.
• 2、 Ahlbrecht, Hubertus,Kornetzky, Dieter. "Lithium N-Lithiomethyldithiocarbamates: New N-Alkylaminomethyl Anion Equivalents". . p. 775 - 777. Retrieved 2007/10/02.