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4-Bromobenzyltrimethylammonium bromide

Base Information
  • Chemical Name:4-Bromobenzyltrimethylammonium bromide
  • CAS No.:25251-62-1
  • Molecular Formula:C10H15 Br N . Br
  • Molecular Weight:309.044
  • Hs Code.:2923900090
  • DSSTox Substance ID:DTXSID30948103
  • Mol file:25251-62-1.mol
4-Bromobenzyltrimethylammonium bromide

Synonyms:4-Bromobenzyltrimethylammonium bromide;WV 560 [German];(p-Bromobenzyl)trimethylammonium bromide;25251-62-1;N-(p-Bromobenzyl)-N,N,N-trimethylammonium bromide;AMMONIUM, (p-BROMOBENZYL)TRIMETHYL-, BROMIDE;WV 560;C10H15BrN.Br;SCHEMBL22265002;DTXSID30948103;Trimethyl-p-Brombenzylammoniumbromid;LS-16930;(4-Bromophenyl)-N,N,N-trimethylmethanaminium bromide

Suppliers and Price of 4-Bromobenzyltrimethylammonium 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 4 raw suppliers
Chemical Property of 4-Bromobenzyltrimethylammonium bromide
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:0.00000 
  • Density:g/cm3 
  • LogP:-0.34070 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:2
  • Exact Mass:308.95508
  • Heavy Atom Count:13
  • Complexity:131
Purity/Quality:

97% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C[N+](C)(C)CC1=CC=C(C=C1)Br.[Br-]
Technology Process of 4-Bromobenzyltrimethylammonium bromide

There total 3 articles about 4-Bromobenzyltrimethylammonium 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:
In tetrahydrofuran; ethanol; at 25 ℃; for 24h; Inert atmosphere;
DOI:10.1055/s-0035-1562344
Guidance literature:
In tetrahydrofuran; at 20 ℃; for 24h;
DOI:10.1016/j.ica.2020.119654
Guidance literature:
With sodium bromide; In water; at 23 ℃; for 132h; Rate constant; Product distribution; pH 4; other reagents ratio;
DOI:10.1021/ja00383a008
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