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Definition
: A group of dipyridinium chloride derivatives that are used as oxidation-reduction indicators. The general formula is 1,1'-di-R-4,4'-bipyridinium chloride, where R
oxidation-reduction indicators
Examples
Benzyl Viologen
Substance
CAS Registry & name
Categories
Source
Drugs
*
N,N'-
bis(3-
sulfonatopropyl)-
4,4'-
bipyridinium
0
*Alkanesulfonates
*Viologens.
ChemSusChem 2010;3(1):97-105
1,1'-
diheptyl-
4,4'-
bipyridinium
0
*Viologens
Ryanodine Receptor Calcium Release Channel.
Br J Pharmacol 1994 Aug;112(4):1216-22
phenyl viologen
0
*Biphenyl Compounds
*Viologens.
J Org Chem 2005 Jun 24;70(13):5028-35
N-
hexyl-
N'-
(4-
vinylbenzyl)-
4,4'-
bipyridinium
0
*Viologens.
Biomaterials 2005 Feb;26(5):501-8
1,1'-
dimethyl-
2,2'-
dicyano-
4,4'-
bipyridinium, bis-
methylsulfate
0
*Nitriles
*Pyridines
Viologens.
Arch Biochem Biophys 1998 Jun 1;354(1):65-72
N,N'-
tetramethylene-
2,2'-
bipyridinium
0
*Viologens.
Photochem Photobiol 1995 Jul;62(1):51-4
N,N'-
dipropyl-
4,4'-
bipyridinium sulfonate
77951-49-6
*Viologens.
Photochem Photobiol 1995 Jul;62(1):51-4
N,N'-
dimethyl-
6-
(2-
pyridinium)phenanthridinium
0
*Phenanthridines
*Viologens.
J Biomol Struct Dyn 1995 Feb;12(4):827-46
N,N'-
propylene-
6-
(2-
pyridinium)phenanthridinium
0
*Phenanthridines
*Viologens.
J Biomol Struct Dyn 1995 Feb;12(4):827-46
N,N'-
ethylene-
6-
(2-
pyridinium)phenanthridinium
0
*Phenanthridines
*Viologens.
J Biomol Struct Dyn 1995 Feb;12(4):827-46
polymeric viologens
0
*Polymers
*Viologens.
Can J Biochem 1979;57(8):1093