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Dibutylammonium bromide

Base Information
  • Chemical Name:Dibutylammonium bromide
  • CAS No.:10435-44-6
  • Molecular Formula:C8H19 N . Br H
  • Molecular Weight:210.157
  • Hs Code.:
  • European Community (EC) Number:233-918-7
  • Mol file:10435-44-6.mol
Dibutylammonium bromide

Synonyms:Dibutylammonium bromide;dibutylazanium;bromide;10435-44-6;1-Butanamine, N-butyl-,hydrobromide (1:1);C8H19N.BrH;dibutylam-monium bromide;di-n-butylammonium bromide;SCHEMBL3467196;YCGYSDWVARRPFG-UHFFFAOYSA-N

Suppliers and Price of Dibutylammonium bromide
Supply Marketing:
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
Total 11 raw suppliers
Chemical Property of Dibutylammonium bromide
Chemical Property:
  • Vapor Pressure:2.1mmHg at 25°C 
  • Boiling Point:163°Cat760mmHg 
  • Flash Point:41.1°C 
  • PSA:12.03000 
  • Density:g/cm3 
  • LogP:3.52520 
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:6
  • Exact Mass:209.07791
  • Heavy Atom Count:10
  • Complexity:37.8
Purity/Quality:

97% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCC[NH2+]CCCC.[Br-]
Technology Process of Dibutylammonium bromide

There total 5 articles about Dibutylammonium bromide 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:
Guidance literature:
With hydrogen bromide;
Guidance literature:
In acetonitrile; at 25 ℃; Rate constant; Mechanism;
Guidance literature:
In acetonitrile; at 25 ℃; Rate constant; Product distribution; Mechanism; the effect of steric and electronic structure of the amine;
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