Bleaching and dyeing; fluid treatment and chemical modification – Dyeing involving animal-derived natural fiber material ,... – Hair dyeing
Patent
1996-02-16
1998-01-06
Lieberman, Paul
Bleaching and dyeing; fluid treatment and chemical modification
Dyeing involving animal-derived natural fiber material ,...
Hair dyeing
8406, 548508, A61K 713
Patent
active
057049491
ABSTRACT:
The present invention is directed to the preparation of an aqueous hair dyeing composition containing an effective hair dyeing amount--at least 2 mg/ml--5,6-dihydroxyindole (DHI). An aqueous hair dyeing composition is produced by reacting under essentially anaerobic conditions dopa or a salt thereof with an alkali metal ferricyanide oxidant in an aqueous reaction medium to obtain dopachrome, and permitting the dopachrome to undergo rearrangement in the aqueous medium to form 5,6-dihydroxyindole, said rearrangement being conducted in the substantial absence of oxidant, the aqueous medium being buffered by sufficient buffering agent to maintain a pH of from about 4.5 to about 9 for the reaction medium throughout the series of reactions that take place thereafter, removing the ferrocyanide species present in the aqueous system, and lastly, charging the composition into a suitable container.
REFERENCES:
patent: 4776857 (1988-10-01), Carroll et al.
patent: 4808190 (1989-02-01), Grollier et al.
patent: 4888027 (1989-12-01), Grollier et al.
patent: 4900326 (1990-02-01), Grollier
patent: 5173085 (1992-12-01), Brown et al.
patent: 5273550 (1993-12-01), Prota et al.
patent: 5279617 (1994-01-01), Prota et al.
patent: 5279618 (1994-01-01), Prota et al.
patent: 5435810 (1995-07-01), Prota et al.
patent: 5441542 (1995-08-01), Prota et al.
patent: 5486619 (1996-01-01), Wenke et al.
patent: 5492541 (1996-02-01), Murphy et al.
patent: 5516916 (1996-05-01), Murphy et al.
Nature, "Synthesis of 5,6-Dihydroxyindole Derivatives: an Oxio-reduction Rearrangement Catalyzed by Zinc Ions," Harley-Mason et al., pp. 1036-1037, Dec. 1950.
J. Chem. Soc., "Melanin and Its Precursors. Part III. New Synthesis of 5,6-Dihydroxyindole and its Derivatives," Bu'Lock et al., pp. 2248-2252, 1951 (no month avail.).
Gazzetta Chimica Italiana, "A Re-examination of the Zinc-Catalyzed Rearrangement of Dopachrome Using Immobilized Tyrosinase," Napolitano et al., p. 357, 1985 (no month avail.).
Biochem. Biophys. Acta., "Effect of Metal Ions on the Rearrangement on Dopachrome," Palumbo et al., pp. 203-209, 1987 (no month avail.).
Analytical Biochemistry, "Preparation of Eumelanin-Related Metabolites 5,6-Dihydroxyindole, 5,6-Dihydroxyindole-2-carboxylic Acid, and Their o-Methyl Derivatives," Wakamatsu et al., pp. 335-340, 1988 (no month avail.).
Prota Giuseppe
Wenke Gottfried
Wolfram Leszek
Clairol Incorporated
Dusheck Caroline L.
Lieberman Paul
Zeller Charles J.
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