1-Pentylpiperidine

Base Information

• Chemical Name: 1-Pentylpiperidine
• CAS No.: 10324-58-0
• Molecular Formula: C10H21 N
• Molecular Weight: 155.283
• European Community (EC) Number: 286-144-7
• DSSTox Substance ID: DTXSID60145709
• Nikkaji Number: J50.675C
• Wikidata: Q83010281
• Mol file: 10324-58-0.mol

Synonyms:1-Pentylpiperidine;PIPERIDINE, 1-PENTYL-;N-Amylpiperidine;N-Pentylpiperidine;Pentylpiperidine;10324-58-0;BRN 0103867;5-20-02-00031 (Beilstein Handbook Reference);1-Amyl piperidine;1-pentyl-piperidine;SCHEMBL44723;DTXSID60145709;EINECS 286-144-7;AKOS006241949;85187-53-7;LS-115863

Chemical Property of 1-Pentylpiperidine

Chemical Property:

• Vapor Pressure: 0.363mmHg at 25°C
• Refractive Index: 1.4498
• Boiling Point: 198.3°Cat760mmHg
• Flash Point: 78.3°C
• Density: 0.841g/cm³
• XLogP3: 2.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 155.167399674
• Heavy Atom Count: 11
• Complexity: 84.9

Purity/Quality:

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

1-PENTYLPIPERIDINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCN1CCCCC1

Technology Process of 1-Pentylpiperidine

There total 13 articles about 1-Pentylpiperidine 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: 8.5%

piperidine (110-89-4) + 1-Pentyl-1-hexylamine (41495-45-8) → 1-pentylpiperidine (10324-58-0) + 1-hexylpiperidine (7335-01-5) + hexan-1-amine (111-26-2) + dihexylamine (143-16-8) + n-Pentylamine (110-58-7) + Di-n-amylamine (2050-92-2)

Guidance literature:

With hydrogen; sulphidized CoO-MoO₃; at 300 ℃; for 1h; under 45003.6 Torr; Mechanism; Product distribution;

Reference yield: 5.8%

1-hexylpiperidine (7335-01-5) → piperidine (110-89-4) + 1-pentylpiperidine (10324-58-0) + 1-Pentyl-1-hexylamine (41495-45-8) + dihexylamine (143-16-8) + Di-n-amylamine (2050-92-2) + pentane (109-66-0,8031-35-4,9078-70-0)

Guidance literature:

With hydrogen; sulphidized CoO-MoO₃; at 300 ℃; for 8h; under 45003.6 - 90757.2 Torr; Mechanism; Product distribution;

Reference yield:

piperidine (110-89-4) → sulfure de pentamethylene (1613-51-0) + 2-methylthiolane (1795-09-1) + pyridine (110-86-1) + 1-pentylpiperidine (10324-58-0) + n-pentanethiol (110-66-7)

Guidance literature:

With hydrogen sulfide; hydrogen; sulfidized Ni-W; at 300 ℃; for 5h; under 105008 Torr; Product distribution;

upstream raw materials:

piperidine

1-Pentyl-1-hexylamine

pyridine

formic acid

Downstream raw materials:

piperidine

N-(2-pentyl)piperidine

N-(1-ethylpropyl)piperidine

n-Pentylamine

Refernces

• 1、 Elkamel,Elidrissi,Yacoubi,Nadiri,Abouarnadasse. "Pyridine hydrodenitrogenation catalysed, under atmospheric pressure, by Ni and Mo oxynitrides and MoNi, MoPNi, AlNi and AlPNi mixed oxynitrides". . p. 2157 - 2179. Retrieved 2007/10/03.
• 2、 Glebov,Kliger,Shuikin,Zaikin. "Reaction of tetrahydrofurfuryl alcohol with ammonia and hydrogen on heterogeneous catalysts". . p. 346 - 352. Retrieved 2007/10/03.