Method for the simultaneous permanent shaping and dyeing of keratinic fibers

US10219994B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10219994-B2
Application numberUS-201715487829-A
CountryUS
Kind codeB2
Filing dateApr 14, 2017
Priority dateOct 15, 2014
Publication dateMar 5, 2019
Grant dateMar 5, 2019

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A method for the permanent shaping and color modification of keratinic in a single process includes the following steps. First, an aqueous composition, including at least one keratin-reducing compound and at least one alkalizing agent, is applied to the keratinic fibers and is left on the keratinic fibers for a period of 5 to 50 minutes at a temperature of 20 to 45° C. The keratinic fibers are rinsed, and optionally dried. Next, a composition including at least one oxidation dye precursor and at least one oxidizing agent is applied to the keratinic fibers and the keratinic fibers are deformed. That composition is allowed to act for 10 to 35 minutes. An aqueous composition including at least one oxidizing agent, is applied to the keratinic fibers for 30 seconds to 15 minutes. The keratinic fibers are rinsed out, along with removal of the deformation aids.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for the permanent shaping and color modification of keratinic fibers in a single process, the method comprising the following method steps in the stated sequence: a) applying an aqueous composition (M1), including 5 to 20% by weight based on a total weight of (M1) of at least one keratin-reducing compound including monoethanolamine thioglycolate, and including 1.5 to 7% by weight based on a total weight of (M1) of at least one alkalizing agent including monoethanolamine and sodium hydrogen carbonate, to the keratinic fibers and leaving this composition (M1) on the keratinic fibers for a period of 5 to 30 minutes at a temperature of 20 to 45° C., b) rinsing the keratinic fibers, and leaving the keratinic fibers damp with perceptible residual moisture so there are no dry keratinic fibers, c) applying a composition (M2), including 0.1 to 5% by weight based on a total weight of (M2) of at least one oxidation dye precursor comprising a developer type precursor that is p-toluylenediamine and comprising a coupler type precursor that is resorcinol, and 4.0 to 12% by weight, based on the total weight of the composition (M2) of at least one oxidizing agent comprising hydrogen peroxide, calculated based on 100% H 2 O 2 , to the damp keratinic fibers and deforming the keratinic fibers, using deformation aids, d) allowing the composition (M2) applied in method step c) to act for 10 to 35 minutes, e) applying an aqueous composition (M3), including 1.5 to 4.0% by weight, based on the total weight of the composition (M3) of at least one oxidizing agent comprising hydrogen peroxide, calculated based on 100% H 2 O 2 , to the keratinic fibers and leaving this composition (M3) on the keratinic fibers for 30 seconds to 15 minutes, f) rinsing the keratinic fibers with removal of the deformation aids, and g) optionally applying an after-treatment agent to the keratinic fibers. 2. The method according to claim 1 , wherein the deformation aids used in method step c) have a diameter of 1 to 10 cm. 3. The method according to claim 1 , wherein the composition (M1) used in method step a) further includes at least one compound selected from the group consisting of sodium hydroxide, potassium hydroxide, ammonia, and 2-amino-2-methylpropane. 4. The method according to claim 1 , wherein the composition (M3) used in method step e) has a pH of 1 to 7 at 20° C. 5. The method according to claim 1 , wherein the step of leaving the composition (M1) on the keratinic fibers for a period of 5 to 30 minutes occurs at room temperature. 6. The method according to claim 1 , wherein the aqueous composition (M1) further includes a non-ionic surfactant comprising decyl glucoside in an amount of from 0.5 to 5% by weight, based on the total weight of the composition (M1). 7. The method according to claim 1 , wherein the aqueous composition (M1) further includes orange oil in an amount of from 0.01 to 0.1% by weight, based on the total weight of the composition (M1). 8. The method according to claim 1 , wherein the aqueous composition (M1) has a pH of from 5 to 9.5 at 20° C. 9. The method according to claim 1 , consisting essentially of the method steps a)-f) in the stated sequence. 10. The method according to claim 1 , consisting of the method steps a)-f) in the stated sequence. 11. The method according to claim 1 , wherein the at least one keratin-reducing compound further includes at least one compound chosen from the group comprising thiolactic acid and cysteine, and the salts thereof. 12. The method according to claim 1 , wherein the at least one keratin-reducing compound further includes at least one compound chosen from the group comprising thiomalic acid, phenylthioglycolic acid, mercaptoethanesulfonic acid, and the salts and esters thereof, cysteine, cysteine, Bunte salts and salts of sulfurous acid, alkali disulfites, hydrogen sulfites, magnesium, ammonium, or alkanolammonium salts based on a C 2 -C 4 mono-, di-, or trialkanolamine, and sulfites as alkali, ammonium, or alkanolammonium salts based on a C 2 -C 4 mono-, di-, or trialkanolamine. 13. The method according to claim 1 , wherein the at least one oxidation dye precursor further includes a coupler type precursor that is 2-methylresorcinol, 2-amino-3-hydroxypyridine, 3-aminophenol, and the physiologically acceptable salts thereof and the mixtures thereof. 14. The method according to claim 1 , wherein the aqueous composition (M3) includes an acid chosen from dipicolinic acid, citric acid, acetic acid, malic acid, lactic acid, tartaric acid, hydrochloric acid, phosphoric acid, pyrophosphoric acid, sulfuric acid, and mixtures thereof. 15. The method according to claim 1 , wherein the step of leaving the composition (M1) on the keratinic fibers occurs for a period of 20 to 40 minutes. 16. The method according to claim 1 , wherein the step of allowing the composition (M2) applied in method step c) to act occurs for 20 to 25 minutes. 17. A method for the permanent shaping and color modification of keratinic fibers in a single process, the method comprising the following method steps in the stated sequence: a) applying an aqueous composition (M1), including at least one keratin-reducing compound and at least one alkalizing agent, to the keratinic fibers and leaving this composition (M1) on the keratinic fibers for a period of 5 to 50 minutes at a temperature of 20 to 45° C., b) rinsing the keratinic fibers, and leaving the keratinic fibers damp with perceptible residual moisture so there are no dry keratinic fibers, c) applying a composition (M2), including at least one oxidation dye precursor and at least one oxidizing agent, to the damp keratinic fibers and deforming the keratinic fibers, using deformation aids, d) allowing the composition (M2) applied in method step c) to act for 10 to 35 minutes, e) applying an aqueous composition (M3), including at least one oxidizing agent, to the keratinic fibers and leaving this composition (M3) on the keratinic fibers for 30 seconds to 15 minutes, f) rinsing the keratinic fibers with removal of the deformation aids, and g) optionally applying an after-treatment agent to the keratinic fibers. 18. The method according to claim 17 , consisting essentially of the method steps a)-f) in the stated sequence. 19. The method according to claim 17 , consisting of the method steps a)-f) in the stated sequence. 20. The method according to claim 17 wherein the aqueous composition (M1) includes 5 to 20% by weight based on a total weight of (M1) of at least one keratin-reducing compound including monoethanolamine thioglycolate, and includes 1.5 to 7% by weight based on a total weight of (M1) of at least one alkalizing agent including monoethanolamine and sodium hydrogen carbonate; and wherein the composition (M2) includes 0.1 to 5% by weight based on a total weight of (M2) of at least one oxidation dye precursor comprising a developer type precursor that is p-toluylenediamine and comprising a coupler type precursor that is resorcinol, and 4.0 to 12% by weight, based on the total weight of the composition (M2) of at least one oxidizing agent comprising hydrogen peroxide, calculated based on 100% H 2 O 2 .

Assignees

Inventors

Classifications

  • Hair-curling or hair-waving appliances (heated curling-tongs, curling-irons A45D1/00 ){; Appliances for hair dressing treatment not otherwise provided for} · CPC title

  • Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof · CPC title

  • containing sulfuric acid derivatives, e.g. sodium lauryl sulfate · CPC title

  • with carboxyl groups directly bound to carbon atoms of aromatic rings · CPC title

  • Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6) · CPC title

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What does patent US10219994B2 cover?
A method for the permanent shaping and color modification of keratinic in a single process includes the following steps. First, an aqueous composition, including at least one keratin-reducing compound and at least one alkalizing agent, is applied to the keratinic fibers and is left on the keratinic fibers for a period of 5 to 50 minutes at a temperature of 20 to 45° C. The keratinic fibers are …
Who is the assignee on this patent?
Henkel Ag & Co Kgaa
What technology area does this patent fall under?
Primary CPC classification A61K8/447. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Mar 05 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).