1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide

Base Information

Chemical Name:1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide
CAS No.:36437-30-6
Molecular Formula:2Br*C₂₆H₄₂N₂
Molecular Weight:542.441
Hs Code.:2933399090
DSSTox Substance ID:DTXSID10957773
ChEMBL ID:CHEMBL2031406
Mol file:36437-30-6.mol

Synonyms:36437-30-6;1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide;Octylviologen bromide;1,1-di-n-octyl-4,4-bipyridinium dibromide;1,1'-Dioctyl-4,4'-bipyridinium dibromide;4,4'-BIPYRIDINIUM, 1,1'-DIOCTYL-, DIBROMIDE;1-octyl-4-(1-octylpyridin-1-ium-4-yl)pyridin-1-ium dibromide;1-octyl-4-(1-octylpyridin-1-ium-4-yl)pyridin-1-ium;dibromide;1,1-Di-n-Octyl-4,4-bipyridiniumdibromide;1,1'-dioctyl-[4,4'-bipyridine]-1,1'-diium bromide;SCHEMBL599465;C26H42N2.2Br;CHEMBL2031406;DTXSID10957773;GVUBEJANEHZYPA-UHFFFAOYSA-L;C26-H42-N2.2Br;MFCD00060051;AKOS015832977;BS-16663;LS-44653;CS-0149211;D1854;FT-0639321;1,1'-Dioctyl-4,4'-bipyridin-1-ium dibromide;D82224;1,1 '-di-n-octyl-4,4'-bipyridinium dibromide;10.14272/GVUBEJANEHZYPA-UHFFFAOYSA-L.1;A823245;1,1'-dioctyl-4,4'-bipyridine-1,1'-diium bromide;doi:10.14272/GVUBEJANEHZYPA-UHFFFAOYSA-L.1

Suppliers and Price of 1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide

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

TRC
1-Octyl-4-(1-octylpyridin-1-ium-4-yl)pyridin-1-iumDibromide
2.5g
$ 175.00

TCI Chemical
1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide >98.0%(T)
5g
$ 162.00

Oakwood
1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide 96%
1g
$ 50.00

Oakwood
1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide 96%
250mg
$ 25.00

Crysdot
1,1'-Dioctyl-[4,4'-bipyridine]-1,1'-diiumbromide 97%
25g
$ 410.00

Biosynth Carbosynth
1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide
2 g
$ 100.00

Biosynth Carbosynth
1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide
25 g
$ 500.00

American Custom Chemicals Corporation
1,1'-DI-N-OCTYL-4,4'-BIPYRIDINIUM DIBROMIDE 95.00%
5G
$ 229.74

AK Scientific
1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide
5g
$ 268.00

AHH
1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide 98%
25g
$ 528.00

Total 13 raw suppliers

Chemical Property of 1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：7.76000
Density:g/cm³
LogP:0.65760
Storage Temp.:Inert atmosphere,Room Temperature
Water Solubility.:almost transparency
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:15
Exact Mass:542.16943
Heavy Atom Count:30
Complexity:306

Purity/Quality:

97% ^*data from raw suppliers

1-Octyl-4-(1-octylpyridin-1-ium-4-yl)pyridin-1-iumDibromide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Statements: 36/37/38
Safety Statements: 26-36/37/39

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCC[N+]1=CC=C(C=C1)C2=CC=[N+](C=C2)CCCCCCCC.[Br-].[Br-]
General Description 1,1'-DI-N-OCTYL-4,4'-BIPYRIDINIUM DIBROMIDE (also known as Octylviologen bromide or OV2?) is a dicationic bipyridinium derivative that forms stable pseudorotaxanes with cucurbit[7]uril (CB[7]) in aqueous solution, where CB[7] preferentially docks at one of its octyl moieties. 1,1'-DI-N-OCTYL-4,4'-BIPYRIDINIUM DIBROMIDE can undergo photoreduction to form radical species (C8V?·), which tend to dimerize but can be stabilized as monomers when bound to β-cyclodextrin (β-CD), enhancing charge separation and enabling applications such as hydrogen evolution with high quantum yields. Additionally, its asymmetric substitution and ionic nature suggest potential utility in materials science, including ionic liquid crystals and conductive organic salts.

Technology Process of 1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide

There total 3 articles about 1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide 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: 98.0%