“…However, they did not scan at 340-360 nm. Mixtures of psulfoquinones and sulfite have been reported to have absorption maximum of 320-345 nm depending on the pH of the mixture (LuValle, 1952). Our results also showed that bisulfite was able to bleach the violet color of melanochrome, an intermediate colored compound formed in the pathway behveen dopachrome and melanin.…”
Section: Effect Of Bisulfite On the Intermediate Colored Quinonessupporting
The role of bisulfite inhibition on the phenoloxidase (PO) catalyzed melanosis reaction in lobster was investigated. Bisulfite appears to inhibit melanosis by hvo mechanisms: (1) by reacting with intermediate quinones in the melanosis reaction, forming sulfoquinones, and (2) by irreversibly reacting with PO causing complete inactivation. The first mechanism is important because intermediate quinones (dopachrome) are the chroma for spectrophotometric analysis of PO activity.
“…However, they did not scan at 340-360 nm. Mixtures of psulfoquinones and sulfite have been reported to have absorption maximum of 320-345 nm depending on the pH of the mixture (LuValle, 1952). Our results also showed that bisulfite was able to bleach the violet color of melanochrome, an intermediate colored compound formed in the pathway behveen dopachrome and melanin.…”
Section: Effect Of Bisulfite On the Intermediate Colored Quinonessupporting
The role of bisulfite inhibition on the phenoloxidase (PO) catalyzed melanosis reaction in lobster was investigated. Bisulfite appears to inhibit melanosis by hvo mechanisms: (1) by reacting with intermediate quinones in the melanosis reaction, forming sulfoquinones, and (2) by irreversibly reacting with PO causing complete inactivation. The first mechanism is important because intermediate quinones (dopachrome) are the chroma for spectrophotometric analysis of PO activity.
“…With pyridine this leads to formation of N-pyridinium sulfonate (19). The reaction of hydroquinone with sulfite in the presence of oxygen is perhaps the most studied (20,21), since sulfite was used as a preservative in hydroquinone-based photographic developers (22). In this system two types of reaction appear to take place: (a) oxidation of the hydroquinone by sulfite radicals and by molecular oxygen, and (b) sulfonation of the quinone to form hydroquinone sulfonates (followed by oxidation ofthe latter to quinone sulfonates) (21).…”
Section: Chemical Transformations Induced By Sulfite Oxidationmentioning
The free-radical chemistry of sulfite oxidation is reviewed. Chemical transformations of organic and biological molecules induced by sulfite oxidation are summarized. The kinetics of the free-radical oxidations of sulfite are discussed, as are the kinetics of the reactions of the sulfite-derived radicals A03 and the peroxy derivative S(6 with organic compounds.
“…Most rate data regarding reactions where an amino group in an aromatic ring is displaced by a nucleophile were obtained as secondary reactions in other studies. 4 The low reactivity of compounds of the type 2 toward attack at carbon 1 is considered to be a consequence of the interaction of the lone pair of electrons on the nitrogen (2) Buncel, E.; Norris, A. R.; Russell, K. E.; Sheridan, P. J. Con. J. Chem.…”
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