K. Imai et al., AVAILABILITY OF FLUOROGENIC REAGENTS HAVING A BENZOFURAZAN STRUCTURE IN THE BIOSCIENCES, Analytica chimica acta, 290(1-2), 1994, pp. 3-20
Fluorogenic reagents having a 2,1,3-benzoxadiazole (benzofurazan) moie
ty are reviewed in terms of reactivity, fluorescence characteristics,
sensitivity and applicability in the biosciences. Those included are 4
-fluoro-7-nitrobenzofurazan (NBD-F), ethylaminosulphonyl)-7-fluoro-2,1
,3-benzoxadiazole (DBD-F), 4-aminosulphonyl-7-fluoro-2,1,3-benzoxadiaz
ole (ABD-F), ammonium 7-fluoro-2,1,3-benzoxadiazole-4-sulphonate (SBD-
F), 4-hydrazino-7-nitro-2,1,3-benzoxadiazole (NBD-H), 4-hydrazino-7-ni
tro-2,1,3-benzoxadiazole hydrazine (NBD-H NH2NH2), ylaminosulphonyl)-7
-hydrazino-2,1,3-benzoxadiazole (DBD-H), 4-aminosulphonyl-7-hydrazino-
2,1,3-benzoxadiazole (ABD-H), 4-nitro-7-N-piperazino-2,1,3-benzoxadiaz
ole (NBD-PZ), ro-7-(2-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole (D-NB
D-APy), ro-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole (L-NBD-APy)
, -dimethylamino-7-N-piperazino-2,1,3-benzoxadiazole (DBD-PZ), -dimeth
ylamino-7-N-cadaverino-2,1,3-benzoxadiazole (DBD-CD), osulphonyl)-7-(1
-piperazynyl)-2,1,3-benzoxadiazole (ABD-PZ), honyl)-7-(5-aminopentylam
ino)-2,1,3-benzoxadiazole (ABD-AP), inosulphonyl)-7-(2-aminoethyl)2,1,
3-benzoxadiazole (ABD-AE) and ammonium 7-N-piperazino-2,1,3-benzoxadia
zole-4-sulphonate (SBD-P2). Their application data in liquid chromatog
raphy are listed in tables. Future trends for the benzofurazan reagent
s are discussed.