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3-AMINOHEXANE

Base Information Edit
  • Chemical Name:3-AMINOHEXANE
  • CAS No.:16751-58-9
  • Molecular Formula:C6H15 N
  • Molecular Weight:101.192
  • Hs Code.:
  • Mol file:16751-58-9.mol
3-AMINOHEXANE

Synonyms:Butylamine,1-ethyl- (8CI); 3-Aminohexane; 3-Hexylamine

Suppliers and Price of 3-AMINOHEXANE
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • HEXAN-3-AMINE 95.00%
  • 10G
  • $ 1679.66
  • American Custom Chemicals Corporation
  • HEXAN-3-AMINE 95.00%
  • 5G
  • $ 1138.78
  • American Custom Chemicals Corporation
  • HEXAN-3-AMINE 95.00%
  • 1G
  • $ 721.59
Total 8 raw suppliers
Chemical Property of 3-AMINOHEXANE Edit
Chemical Property:
  • Vapor Pressure:16mmHg at 25°C 
  • Melting Point:-40.7°C (estimate) 
  • Refractive Index:1.4200 
  • Boiling Point:119.3°Cat760mmHg 
  • PKA:11.00±0.35(Predicted) 
  • Flash Point:25.2°C 
  • PSA:26.02000 
  • Density:0.768g/cm3 
  • LogP:2.22410 
Purity/Quality:

98%min *data from raw suppliers

HEXAN-3-AMINE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 3-AMINOHEXANE

There total 14 articles about 3-AMINOHEXANE 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: 58.0%

Guidance literature:
Guidance literature:
With ammonium acetate; sodium cyanoborohydride; at 20 ℃; for 24h;
Guidance literature:
hexane; With cerium(III) chloride; 1,1,1-trichloroethanol; di-tert-butyl-diazodicarboxylate; tetrabutyl-ammonium chloride; In acetonitrile; at 20 ℃; for 12h; Irradiation; Inert atmosphere; Sealed tube;
With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 1h;
With hydrogen; In methanol; for 12h; Reagent/catalyst;
DOI:10.1021/jacs.0c00212
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