2-n-Butylaminonaphthazarin (2) absorbs at 499 and 532 nm in ethanol bu
t at 539 and 577 nm in alkali solution, while 2,6-bis(n-butylamino)nap
hthazarin (3) absorbs at 461, 500 and 540 nm in ethanol but at 511 and
545 nm in alkali solution, with only a small bathochromic shift of 5
nm. The absorption curve of 3 was changed by addition of alkali and th
e lambda(max) at around 461 nm completely disappeared. In the case of
2-bromo-3,6-bis(n-butylamino)naphthazarin (4), tautomerism between the
1,4-quinone and 1,5-quinone forms was observed and the isosbestic poi
nt was observed at 480 nm. Dye 2 easily deprotonated to give the 1,4-d
ianion, but dyes 3 and 4 existed as tautomeric mixtures in solution an
d shifted to 1,5-quinone forms in alkali solution.