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Bromotrimethylammoniumbimane Bromide

Base Information
  • Chemical Name:Bromotrimethylammoniumbimane Bromide
  • CAS No.:71418-45-6
  • Molecular Formula:Br*C13H19BrN3O2
  • Molecular Weight:409.121
  • Hs Code.:2933998090
  • European Community (EC) Number:615-289-4
  • DSSTox Substance ID:DTXSID70332981
  • Mol file:71418-45-6.mol
Bromotrimethylammoniumbimane Bromide

Synonyms:71418-45-6;qBBr;Bromotrimethylammoniumbimane Bromide;Bromotrimethylammoniumbimame bromide;Monobromotrimethylammoniobimane bromide;[7-(bromomethyl)-2,6-dimethyl-3,5-dioxopyrazolo[1,2-a]pyrazol-1-yl]methyl-trimethylazanium;bromide;1-(5-(Bromomethyl)-2,6-dimethyl-1,7-dioxo-1H,7H-pyrazolo[1,2-a]pyrazol-3-yl)-N,N,N-trimethylmethanaminium bromide;Thiolyte MQ;MFCD00036953;Monobromotrimethylammoniobimane, bromide;DTXSID70332981;AKOS030254629;Monobromo(trimethylammonio)bimane bromide;FT-0628975;Monobromo(trimethylammonio)bimane bromide, suitable for fluorescence, >=90.0% (HPLC);(7-Bromomethyl-2,6-dimethyl-3,5-dioxo-3H,5H-pyrazolo[1,2-a!pyrazol-1-ylmethyl)-trimethyl-ammonium, bromide;[7-(bromomethyl)-2,6-dimethyl-3,5-dioxo-pyrazolo[1,2-a]pyrazol-1-yl]methyl-trimethyl-ammonium;1H,7H-Pyrazolo[1,2-a]pyrazole-3-methanaminium,5-(bromomethyl)-N,N,N,2,6-pentamethyl-1,7-dioxo-,bromide(1:1)

Suppliers and Price of Bromotrimethylammoniumbimane 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
  • Usbiological
  • Bromotrimethylammoniumbimane Bromide
  • 25mg
  • $ 355.00
  • Usbiological
  • Bromotrimethylammoniumbimane bromide
  • 10mg
  • $ 340.00
  • TRC
  • BromotrimethylammoniumbimaneBromide
  • 25mg
  • $ 90.00
  • Sigma-Aldrich
  • Monobromo(trimethylammonio)bimane bromide suitable for fluorescence, ≥90.0% (HPLC)
  • 25 mg
  • $ 286.00
  • Sigma-Aldrich
  • Monobromo(trimethylammonio)bimane bromide suitable for fluorescence, ≥90.0% (HPLC)
  • 25mg-f
  • $ 277.00
  • Medical Isotopes, Inc.
  • BromotrimethylammoniumbimaneBromide
  • 125 mg
  • $ 1480.00
  • Biosynth Carbosynth
  • Bromotrimethylammoniumbimane bromide
  • 50 mg
  • $ 195.00
  • Biosynth Carbosynth
  • Bromotrimethylammoniumbimane bromide
  • 25 mg
  • $ 105.00
  • Biosynth Carbosynth
  • Bromotrimethylammoniumbimane bromide
  • 10 mg
  • $ 65.00
  • Biosynth Carbosynth
  • Bromotrimethylammoniumbimane bromide
  • 250 mg
  • $ 875.00
Total 6 raw suppliers
Chemical Property of Bromotrimethylammoniumbimane Bromide
Chemical Property:
  • Melting Point:222-228°C (dec.) 
  • PSA:42.96000 
  • LogP:-2.08110 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:DMSO: 5 mg/mL 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:408.98235
  • Heavy Atom Count:20
  • Complexity:529
Purity/Quality:

>98% *data from raw suppliers

Bromotrimethylammoniumbimane Bromide *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: 22-24/25 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CC1=C(N2C(=C(C(=O)N2C1=O)C)CBr)C[N+](C)(C)C.[Br-]
  • Uses BroMotriMethylaMMoniuMbiMane BroMide is a charged fluoresent sulfhydryl active reagent. Bromotrimethylammoniumbimane is a derivative of monobromobimane containing a positive charge which permits separation of its conjugates by electrophoresis or cation-exchange chromatography. The membrane permeability of this charged bimane as well as its ability to access sites within a protein may differ from that of the uncharged bimane probes. These reagents are also useful for detecting the distribution of protein thiols in cells before and after chemical reduction with disulfides. Fluorescence: max. Abs. l = 398nm, max. Em. l = 475-485 (when reacted with thiol); e x 10-3: 5.0
Technology Process of Bromotrimethylammoniumbimane Bromide

There total 1 articles about Bromotrimethylammoniumbimane 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:
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