Stabilized color depositing shampoo

Abstract
A composition for coloring and shampooing hair substantially free, preferably totally and completely free, of anionic surfactants, comprising at least one cationic dye, n-methyl alkyl glucamide with a carbon chain length from 8 and 20, inclusive, preferably 8 and 10, an aqueous carrier, and at least one stabilizer of anti-oxidant and free radical scavanger. By weight, (based on the total weight of the composition), the composition comprises 0.0005% to 3.0% cationic dye, 2.5 to 30% n-methyl alkyl glucamide, 30 to 70% water, and 0.01 to 0.5% stabilizers of anti-oxidant and free radical scavenger. The present invention relates to hair cleaning compositions containing at least one cationic dye, a nonionic or amphoteric surfactant, a fragrance, and a stabilizer (antioxidant).
Description
FIELD OF THE INVENTION

The present invention relates to compositions for coloring and cleansing hair using a one-part formulation. More specifically, the invention relates to shampoo compositions containing at least one cationic dye, a nonionic or amphoteric surfactant, a fragrance, and a combination of two stabilizers (antioxidants). For a specific embodiment with a particular nonionic surfactant, the invention provides a color depositing shampoo with improved foaming ability compared to existing color depositing shampoo products.


BACKGROUND

Basic cationic hair dyes have been available for use in cosmetic products for more than twenty years. They have been adapted for use in color refreshing shampoo and conditioners, temporary hair color gels, and cremes. The products are intended to enhance and refresh previously colored hair, neutralize an unwanted shade, bring new highlights, and create visible color change.


One of the main drawbacks for cationic dyes in many types of hair care products is they are not useful in combination with or within products containing anionic ingredients, particularly anionic surfactants. The combination of cationic dyes and anionic ingredient(s) in a single product, e.g., a color depositing shampoo, causes a reduction of foaming properties (in a shampoo, foaming is recognized as being a desirable attribute. A shampoo that does not foam or does not foam adequately or with a suitable foam quality generally has perceived consumer negatives) and reduced color deposition. The combination of the two could also cause precipitation of an unwanted anionic/cationic complex. Common industry practice therefore utilizes high levels/quantities of cationic dyes in order to compensate for these drawbacks while still achieving a desired level of color deposition. Consequently, existing color depositing shampoos must use greater amounts of dye in the products to account for the “waste” causing higher costs of goods and thus higher retail prices effectively rendering combined cationic dye with anionic surfactant products highly difficult to market.


The current industry alternative for color depositing shampoos is a combination of a cationic dye with amphoteric and/or nonionic surfactants. Those products do not suffer from the above stated disadvantages arising primarily from the opposing ionic charges of the dye and surfactant. Here again, however, there are well known disadvantages. One problem with coloring shampoos which are generally free of anionic surfactants (that is, they are based on nonionic, amphoteric and/or cationic surfactants) is that they have a tendency not to foam adequately or may have poor sensory properties associated with the foaming, such as a tendency for any foam that does generate to generate slowly, spread slowly, or to dissipate quickly. The viscosity of the product(s) is also difficult to control. Addition of a small amount of an anionic surfactant (which adds to the production steps and increases cost of goods) is sometimes done to improve the foaming properties of a dye product made with a nonionic, amphoteric and/or cationic surfactants, knowing the resulting product will suffer from decreased dye deposition and/or suffer long term stability issues such as tonal shifts, precipitation or separation.


Thus there is a need for a color depositing shampoo made with cationic dyes that is substantially free from anionic surfactants with good foaming properties to efficiently and effectively deliver the dyes to the hair. It would be highly beneficial to have a color depositing shampoo that can achieve equal, if not more, dye deposition (and thus color change) compared to existing products, using less dye within the compositions of those existing products. There is a need for a color depositing shampoo that has less waste of dye when used. There is a need for a lower cost to manufacture color depositing shampoo that can effectively deposit color with good foaming properties.


It is thus an object of the present invention to provide a shampoo based formulation that will efficiently color the hair and effectively clean the hair. It is also an object of the invention to provide a shampoo based formulation that will replace ordinary shampoo but also be useful as a hair dye, a composition with improved and more desirable foaming properties.


In addition, basic, cationic dyes are organic dyes that can undergo both oxidative and reductive processes. The reaction that leads to a reduction of a dye molecule by a substrate usually involves an electron or hydrogen atom transfer from the reducing agent to the dye. Free radicals are produced in solution and can undergo subsequent redox reactions with the dye molecule, creating a “bleaching” or degradation of the dye molecule. The bleaching or degradation of the dye molecule renders it inactive, creates problems with efficacy and limits the shelf life of a finished hair color product. The free radicals produced in solution are also a result of the oxidative degradation of fragrance oils or other components in the product. Exposure to UV light can also produce free radicals.


Fragrances are present in numerous end-use products, not only fine perfumes but also as additives in a large range of applications. Personal care products including shampoos are typically fragranced to increase consumer acceptability by masking malodors of base ingredients. Fragrance compositions typically contain between 10 and 100 natural and synthetic fragrance molecules encompassing several organic functional groups including alcohols, phenols, aldehydes and ketones, esters and lactone, terpenes, ethers, oximes, ketals, etc. However, some fragrances, in particular terpenes and aldehydes, are very sensitive to oxidation by molecular oxygen. The consequences are not only a loss of sensorial properties, but also the appearance of off-notes and/or undesirable coloring. The oxidation may also develop possible irritation, allergy and sensitivity and free radicals may react with other components within a formula. Fragrance formulators strive to inhibit oxidation by adding antioxidants, such as BHT or other phenolics.


To prevent fragrance molecules from oxidative degradation, different types of antioxidants are commonly used. They can be classified into basically two classes according to the mechanism of action: (1) the primary or chain-breaking antioxidants and (2) the secondary or preventative antioxidants that do not react with the radicals but act as chelators, deactivate singlet oxygen, absorb ultraviolet radiation, or scavenge oxygen itself.


It is common practice in the cosmetic industry to determine (test) the shelf-life and stability of a formulation by placing the product samples at different environmental conditions for a set period of time. The conditions vary in temperature and light levels and are meant to simulate what will happen to the product during its life cycle. At select time intervals the samples are evaluated for various physical, chemical and performance characteristics to see how they have changed. If the changes are minimal to the company standards, the formula is “passed”. This means when the formula is shipped to the customers, it will be as good as when it was first produced. The underlying assumption in stability testing is that increasing storage temperature speeds up aging reactions that will occur. In the cosmetic industry, the “rule of thumb” is that a sample that is stored at 45° C. for 8 weeks is equivalent to one that is stored at room temperature for one year.


Thus there is a need for a color depositing shampoo made with cationic dyes, non-ionic and/or amphoteric surfactant(s), fragrance, and stabilizer that meets desired stability for such a product. There is also a need for a color depositing shampoo made with cationic dyes, non-ionic and/or amphoteric surfactant(s), fragrance, and stabilizer that is substantially free from anionic surfactants with good foaming properties to efficiently and effectively deliver the dyes to the hair.


It is thus an additional object of the present invention to provide a shampoo based formulation that will efficiently color the hair and effectively clean the hair which meets a certain minimum stability testing and meet a desired shelf life. It is also an object of the invention to provide a shampoo based formulation that will replace ordinary shampoo but also be useful as a hair dye, a composition with improved and more desirable foaming properties which also meets a certain minimum stability testing.


SUMMARY OF THE INVENTION

Applicant has invented a composition that overcomes these and other shortcomings. While the invention will be described in connection with certain embodiments, it will be understood that the invention is not limited to those embodiments. To the contrary, the invention includes all alternatives, modifications and equivalents as may be included within the spirit and scope of the present invention.


Applicant has surprisingly discovered that the combination of a specific nonionic surfactant, namely n-methyl alkyl glucamide, with a cationic dye(s) can be used to create an effective and efficient color depositing shampoo with unexpected and desirable foaming properties. Thus, Applicant has discovered that a color depositing shampoo with preferred foaming properties can be made without the need for extra dye and without any anionic surfactant. Applicant has discovered an efficient, effective, lower dye composition, color depositing shampoo with desirable foaming properties comprising a cationic dye and n-methyl alkyl glucamide. Applicant has discovered that use of n-methyl alkyl glucamide with a chain length anywhere from 8 to 20 is possible and included within the scope of the invention, with a C8/C10 carbon chain length most preferred for its lathering properties. The invention allows for efficient dye deposition with commercially acceptable foaming characteristics. The composition of the present invention thus provides unexpected superior results for a shampoo capable of depositing color with desirable foaming.


The present invention relates to the application of cationic dyes to human hair using a one-part shampoo based formulation. The invention is a cleansing and coloring composition that is substantially free, preferably totally and completely free, of anionic surfactants. In one embodiment, said composition according to the invention comprises:

    • (a) at least one cationic dye;
    • (b) n-methyl alkyl glucamide with a carbon chain length between 8 and 20 (C8-C20), inclusive, preferably 8 (C8) and 10 (C10);
    • (c) an aqueous carrier; and
    • (d) at least one stabilizer of anti-oxidant and free radical scavanger.


      Optionally, other ingredients that may be added to the composition but which are not necessary for the composition, include a rheology modifying polymer, conditioning ingredients, and additional surfactants.


The color depositing shampoo composition according to the invention comprises, by weight (all the weight percents are based on the total weight of the composition):

    • (a) 0.0005% to 3.0% cationic dye;
    • (b) 2.5 to 30% n-methyl alkyl glucamide;
    • (c) 30 to 70% water; and
    • (d) 0.01 to 0.5% stabilizers of anti-oxidant and free radical scavenger.


The properties of the invention are surprising and unique over existing technologies because the composition effectively delivers acceptable and efficient color to hair along with a consumer acceptable foam. The color and long term stability of the composition continues to deliver the same amount of color to the hair. Formulas with materials that are anionic deliver less color to the hair and overtime are seen to deliver less or undesirable results. The foaming characteristics of the invention is closer to the amount of foam delivered from a traditional anionic, sulfate shampoo.


Applicant has also discovered the stability and the shelf life of the composition is improved by using a combination of specific stabilizers, namely, Octadecyl Di-t-butyl-4-hydroxyhydrocinnamate and Tris (Tetramethylhydroxypiperidinol) Citrate. This result is particularly applicable when the composition includes a fragrance, specifically either Givaudan UAE17135/00. Accordingly, in one embodiment, said composition according to the invention comprises:

    • (a) at least one cationic dye;
    • (b) n-methyl alkyl glucamide with a carbon chain length between 8 and 20 (C8-C20), inclusive, preferably 8 (C8) and 10 (C10);
    • (c) an aqueous carrier;
    • (d) a combination of stabilizers (Di-t-butyl-4-hydroxyhydrocinnamate and Tris (Tetramethylhydroxypiperidinol) Citrate; and
    • (e) a fragrance (Givaudan UAE17135/00).


The color depositing shampoo composition according to the invention comprises, by weight (all the weight percents are based on the total weight of the composition):

    • (a) 0.0005% to 3.0% cationic dye;
    • (b) 2.5 to 30% n-methyl alkyl glucamide;
    • (c) 30 to 70% water;
    • (d) 0.01 to 0.5% Di-t-butyl-4-hydroxyhydrocinnamate and Tris (Tetramethylhydroxypiperidinol) Citrate; and
    • (e) 0.1 to 2.0% fragrance (Givaudan UAE17135/00).


The present invention also includes the aforementioned compositions with other non-ionic and/or amphoteric surfactants, albeit the color depositing shampoo composition with a different surfactant will most likely exhibit inferior foaming properties than with n-methyl alkyl glucamide.


Applicant has surprisingly found that it is possible to improve the stability and shelf life characteristics in a color depositing shampoo composition including a specific fragrance (Givaudan UAE17135/00) by using two specific stabilizers.





BRIEF DESCRIPTION OF THE DRAWINGS

The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.


The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments of the invention and, together with the general description of the invention given above and the detailed description of an embodiment given below, serve to explain the principles of the present invention. Similar components of the devices are similarly numbered for simplicity.



FIG. 1 illustrates the composition for one example embodiment of the invention with the percentages representing the amount by weight compared to total weight of the composition.



FIG. 2 is a graph showing the foaming properties of n-methyl alkyl glucamide surfactants having different carbon chain lengths.



FIGS. 3 and 5 include pictures of swatches dyed with a composition according to the invention and four other comparative compositions at day 1 and day 21, respectively.



FIGS. 4 and 6 are line graphs showing the change in color for the swatches compared to the control bleached swatch (overall color change ΔE=SQRT(ΔL2+Δa2+Δb2) at day 1 and day 21, respectively.



FIG. 7 contains a table showing the results of the foaming tests for the compositions tested.



FIGS. 8-11 contain tables with the compositions of the comparative examples tested and compared to test results for Applicant's example composition.



FIG. 12 illustrates the composition for a second example embodiment of the invention with the percentages representing the amount by weight compared to total weight of the composition.



FIG. 13 illustrates the composition for one example embodiment of the invention with stabilizers (NB3-93B) and without stabilizers (NB3-93C), with the percentages representing the amount by weight compared to total weight of the composition.



FIG. 14 is a picture of test bottles containing the compositions in FIG. 13 without the stabilizers after four weeks at 50 degrees Celsius, with the stabilizers after four weeks at 4 degrees Celsius, and with the stabilizer after four weeks at 50 degrees Celsius. FIG. 14 also shows the color grading scale for the test samples.



FIG. 15 illustrates the compositions for two example embodiments of the invention (using different cationic dyes) with the percentages representing the amount by weight compared to total weight of the composition.



FIG. 16 is a picture of test bottles containing the compositions in FIG. 15 with the stabilizers, shown at start and after 28 days at 50 degrees Celsius. FIG. 16 also shows the color grading scale for the test samples.



FIG. 17 illustrates the compositions for an example embodiment of the invention using Givaudan UAE17135/00 as the fragrance (Fragrance A) along with the same composition instead using Flavor and Fragrance Specialties F127Z35 as the fragrance (Fragrance B), with the percentages representing the amount by weight compared to total weight of the composition.



FIG. 18 is a picture of test bottles containing the compositions in FIG. 17 with the stabilizers, shown at start and at 28 days at 50 degrees Celsius. FIG. 18 also shows the color grading scale for the test samples.





DETAILED DESCRIPTION OF THE INVENTION

Reference is being made in detail to presently preferred embodiments of the invention. Selective embodiments are provided by way of explanation of the invention, which is not intended to be limited thereto. In fact, those of ordinary skill in the art may appreciate upon reading the present specification and viewing the present drawings that various modifications and variations can be made.


The present invention is a one-part shampoo based composition for cleansing and coloring hair that is substantially free, preferably totally and completely free, of anionic surfactants. In one embodiment, the composition according to the invention comprises:

    • (a) at least one cationic dye;
    • (b) n-methyl alkyl glucamide with a carbon chain length between 8 and 20, inclusive, preferably 8 and 10;
    • (c) an aqueous carrier; and
    • (d) at least one stabilizer of anti-oxidant and free radical scavanger.


Optionally, other ingredients that may be added to the composition but which are not necessary for the composition, include a rheology modifying polymer, conditioning ingredients, and additional surfactants.


The color depositing shampoo composition according to the invention comprises, by weight (all the weight percents are based on the total weight of the composition):

    • (a) 0.0005% to 3.0% cationic dye;
    • (b) 2.5 to 30% n-methyl alkyl glucamide;
    • (c) 30 to 70% water; and
    • (d) 0.01 to 0.5% stabilizers of anti-oxidant and free radical scavenger.


It being understood that the above described compositions are open to the inclusion of other ingredients that may alter the characteristics of the formula without rendering the system inoperative as a color depositing shampoo.


Use of a stabilizer prevents a shift in the color deposition as the product ages and is exposed to heat. The stabilizer consist of an anti-oxidant and free radical scavenger, such as, for example, tocopherol and sodium citrate.


Other active ingredients may include rheology modifiers, fragrances, chelating agents, opacifiers, conditioning ingredients and other adjuvants. Optionally, suitable amphoteric, nonionic and/or cationic surfactants may be added to the compositions of the invention as desired. Compositions of this invention may contain any other non-anionic ingredients normally used in hair shampoos. These other ingredients may include proteins, fragrances, preservatives, thickeners, conditioners, humectants, opacifiers, and/or pH adjustors.



FIG. 1 illustrates the composition for one example embodiment of the invention with the percentages representing the amount by weight compared to total weight of the composition. In FIG. 1, the n-methyl alkyl glucamide has a carbon chain length of eight and ten (C8/C10). Applicant has surprisingly discovered that using a n-methyl alkyl glucamide surfactant with a C8/C10 carbon chain length produces a non-ionic based surfactant shampoo with superior foaming properties when cationic dyes are incorporated to create a color depositing shampoo. As shown in FIG. 2, the foaming properties of a shampoo made from n-methyl alkyl glucamide is greatest when the carbon chain length is C8/C10, and decreases as the carbon chain length increases, such as seen in the results for the C12/C14 and the C12/C18 chain length ranges. The n-methyl alkyl glucamide surfactant used in the composition of an embodiment of the invention is not, however, limited to just the C8/C10 carbon chain length. The invention also includes embodiments comprising other carbon chain lengths of the n-methyl alkyl glucamide surfactant in the composition. For example, an embodiment may include a combination of n-methyl alkyl glucamide surfactant having carbon chain lengths C8 to C12, or C8 to C14, or C12 to C14, and others. Combinations of different carbon chain lengths ranging from C8 to C20 are possible and included in the scope of the invention. The n-methyl alkyl glucamide surfactant may be one from the group consisting of capryloyl/caproyl methyl glucamide, lauroyl/myristoyl methyl glucamide, and cocoyl methyl glucamide. The dye may be at least one from the group consisting of Basic Blue 124, Basic Yellow 87, Basic Red 51, Basic Orange 31, Basic Brown 17, Basic Blue 99, HC Blue 16, HC Blue 15, Basic Violet 2, Basic Brown 16, and Basic Yellow 57.


The compositions of the invention may be made by dispersing the ingredients in water followed by the application of sufficient heat to dissolve the ingredients without causing decomposition. For example, the procedure to create the example composition identified in FIG. 1 is as follows:

    • 1. To vessel, add water and disperse guar hydroxypropyltrimonium chloride with a prop mixer.
    • 2. Add polyacrylate-1 cross polymer with continued mixing.
    • 3. Add surfactants, chelator, preservatives, panthenol and protein.
    • 4. Premix the fragrance and the phytantriol and add to main batch.
    • 5. Adjust pH to between 4.5 and 5.0 with citric acid. Continue mixing for 45 minutes.
    • 6. In a separate vessel, charge water and add dyes. Heat to 60 degrees Celsius and mix until dyes are dissolved. Add to main vessel and mix until uniform.


The superior color depositing and foaming properties of the shampoo according to the invention is depicted by way of a comparison with existing compositions. Applicant's color depositing shampoo according to the example embodiment in FIG. 1 (an illustration of the invention and not intended to limit same) was compared to four other shampoos that impart color to the hair and those products are described in published patent references. For purposes of the comparison, Applicant's composition is identified as “Example 1” and the other compositions are identified as “A”, “B”, “C” and “D”. The compositions were all produced exactly as disclosed in the patent references, and the dye colors were replaced with the same basic cationic dye colors used in Example 1 and in equal amounts, that is 0.13% basic brown 17, 0.13% basic blue 99, and 0.2% basic red 76, for a total dye composition of 0.46% by weight.


Example 1 and all four comparative compositions (A, B, C, and D) were evaluated by the same two tests, one to measure the amount of hair color change resulting from use (the amount of dye deposition), and one to measure foaming.


For the dye deposition measurement test, bleached hair swatches supplied by International Hair Importers were used. Each swatch was dyed out with one of the compositions, the dye out procedure involved one lather of the shampoo with rinsing, followed by blow drying of the swatch. The procedure was repeated after a 21 day period on new swatches. The color was visually assessed at day 1 and at day 21 with side by side comparisons of the swatches. The amount of color change was also measured at day 1 and day 21 on the CIELAB scale using a Hunter Lab Ultra Scan XE Colormeter. FIGS. 3 and 5 include pictures of the swatches at day 1 and day 21, respectively. FIGS. 4 and 6 are line graphs showing the overall color change (ΔE) for the swatches at day 1 and day 21, respectively.


The foaming of each shampoo was assessed by a blender test modified version of ASTM D3519-88 Foam in aqueous media (blender test). 1.0 grams of shampoo was mixed with 99.0 grams deionized water until homogeneous. The shampoo solution was put into a Bodum blender and run on “high” for 60 seconds. The height of the foam was measured. FIG. 7 contains a table showing the results of the foaming test.


Comparative example A is from Tamareselvy et. al. (U.S. Pat. No. 7,378,479), which discloses the combination of the cationic dyes with anionic surfactants (sodium and ammonium laureth sulfates), in combination with amphoteric surfactants (such as cocamidopropyl betaine) and cationic compatible amino-substituted vinyl polymer as a shampoo for color treatment and color maintenance. The composition for A produced and tested is set forth in FIG. 8. As shown in the results, significantly less color deposition occurred on the swatch for A compared to Applicant's Example 1.


Comparative example B is from Kapsner, et. al. (U.S. Pat. No. 6,500,413 B1) which discloses the combination of one or more cationic components in an anionic system provided the predominant anionic surfactant is an alkyl glucoester. The composition for B produced and tested is set forth in FIG. 9. As shown in the results, less color deposition occurred compared to Example 1 and B produced significantly less foaming compared to Example 1.


Comparative example C is from Massoni (U.S. Pat. No. 7,578,857 B1) which discloses use of cationic dyes, amphoteric surfactants, nonionic surfactants and an anionic sarcosinate surfactant for a shampoo coloring formulation. The composition for C produced and tested is set forth in FIG. 10. As shown in the results, less color deposition occurred compared to Example 1 and C produced significantly less foaming compared to Example 1.


Comparative example D is from Schmucker-Castner et. al., (U.S. Pat. No. 7,217,752) which discloses a stable, aqueous composition containing a substantially cross linked alkali-swellable acrylate copolymer rheology modifier, a surfactant, an alkaline material and various compounds requiring suspension or stabilization. Additionally, the reference discloses a phase stable cationic dye composition. The composition for D produced and tested is set forth in FIG. 11. Although the amount of color deposition compared to Example 1 may be close, D provides significantly less foaming than Example 1.


Accordingly, none of the other compositions tested provide the same or an equivalent ability to color hair and foam.


Applicant has also surprisingly discovered that a specific combination of anti-oxidants with specific cationic dyes and fragrance can be used to create an effective and efficient fragranced, color depositing shampoo that remains stable with predictable performance within the shelf life of the product. Applicant has discovered that a color depositing shampoo that contains select cationic dyes, anti-oxidants and free radical scavengers are stable for an expected shelf life. The invention is a cleansing and coloring composition that remains stable over a commercially acceptable shelf life as predicted by accelerated stability testing. In another embodiment of the invention, said composition according to the invention comprises:

    • (a) at least one cationic dye;
    • (b) at least one nonionic or amphoteric surfactant;
    • (c) an aqueous carrier;
    • (d) a combination of stabilizers (Di-t-butyl-4-hydroxyhydrocinnamate and Tris (Tetramethylhydroxypiperidinol) Citrate; and
    • (e) a fragrance (Givaudan UAE17135).


The color depositing shampoo composition according to the invention comprises, by weight (all the weight percents are based on the total weight of the composition):

    • (a) 0.0005% to 3.0% cationic dye;
    • (b) 2.5 to 30% n-methyl alkyl glucamide;
    • (c) 30 to 70% water;
    • (d) 0.01 to 0.5% Di-t-butyl-4-hydroxyhydrocinnamate and Tris (Tetramethylhydroxypiperidinol) Citrate; and
    • (e) 0.1 to 2.0% fragrance (Givaudan UAE17135).


It is being understood that the above-described compositions are open to the inclusion of other ingredients that may alter the characteristics of the formula without rendering the system inoperative as a color depositing shampoo. Use of an anti-oxidant as a stabilizer prevents a shift in the color as the product ages and is exposed to heat. Other ingredients may include rheology modifiers, fragrances, chelating agents, opacifiers conditioning ingredients and other adjuvants. Suitable amphoteric, nonionic and/or cationic surfactants may be added to the compositions of the invention as desired. Compositions of this invention may contain any other non-anionic ingredients normally used in hair shampoos. These ingredients may include proteins, preservatives, thickeners, conditioners, humectants and/or pH adjustors.


The compositions of the invention may be made by dispersing the ingredients in water followed by the application of sufficient heat to dissolve the ingredients without causing decomposition.


It should be understood, of course, that the foregoing relates to exemplary embodiments of the invention and that modifications may be made without departing from the spirit and scope of the present invention.

Claims
  • 1. A one-part coloring depositing shampoo composition for human hair comprising: at least one cationic dye;a nonionic surfactant that is n-methyl alkyl glucamide with carbon chain lengths between 8 and 20;an aqueous carrier;a stablizer comprising a combination of Di-t-butyl-4-hydroxyhydrocinnamate and Tris (Tetramethylhydroxypiperidinol) Citrate;wherein said composition does not contain any anionic surfactant.
  • 2. The composition of claim 1, wherein the composition comprises, by weight: 0.0005% to 3.0% cationic dye;2.5 to 30% n-methyl alkyl glucamide with carbon chain lengths between 8 and 20;30 to 70% aqueous carrier; and0.01 to 0.5% stabilizer comprising a combination of Di-t-butyl-4-hydroxyhydrocinnamate and Tris(Tetramethylhydroxypiperidinol) Citrate.
  • 3. The composition of claim 2, wherein said n-methyl alkyl glucamide is selected from the group consisting of capryloyl/caproyl methyl glucamide, lauroyl/myristoyl methyl glucamide, and cocoyl methyl glucamide.
  • 4. The composition of claim 2, further comprising an amphoteric surfactant.
  • 5. The composition of claim 2, further comprising a thickener.
  • 6. The composition of claim 2, further comprising an opacifier.
  • 7. The composition of claim 2, further comprising a chelating agent.
  • 8. The composition of claim 2, wherein said cationic dye is at least one from the group consisting of Basic Blue 124, Basic Yellow 87, Basic Red 51, Basic Orange 31, Basic Brown 17, Basic Blue 99, HC Blue 16, HC Blue 15, Basic Violet 2, Basic Brown 16, and Basic Yellow 57.
  • 9. The composition of claim 2, wherein said aqueous carrier is water.
  • 10. The composition of claim 1, wherein the composition comprises, by weight less than 0.50% cationic dye.
  • 11. The composition of claim 10, wherein said cationic dye composition is about 0.46% by weight.
  • 12. The composition of claim 11, wherein said n-methyl alkyl glucamide is about 2.5% by weight.
  • 13. A coloring depositing shampoo composition for human hair comprising: a cationic dye;a nonionic surfactant that is n-methyl alkyl glucamide with carbon chain lengths of 8 and 10;an aqueous carrier;a stablizer comprising a combination of Di-t-butyl-4-hydroxyhydrocinnamate and Tris (Tetramethylhydroxypiperidinol) Citrate; andwherein said composition does not contain any anionic surfactant; andwherein said composition comprises, by weight, less than 0.50% cationic dye.
  • 14. The composition of claim 13, wherein the composition comprises, by weight: 2.5 to 30% n-methyl alkyl glucamide with carbon chain lengths of 8 and 10;30 to 70% aqueous carrier; and0.01 to 0.5% stabilizer comprising a combination of Di-t-butyl-4-hydroxyhydrocinnamate and Tris(Tetramethylhydroxypiperidinol) Citrate.
  • 15. The composition of claim 13, wherein said cationic dye is at least one from the group consisting of Basic Blue 124, Basic Yellow 87, Basic Red 51, Basic Orange 31, Basic Brown 17, Basic Blue 99, HC Blue 16, HC Blue 15, Basic Violet 2, Basic Brown 16, and Basic Yellow 57.
  • 16. The composition of claim 15, wherein said cationic dye is about 0.46% by weight of said composition.
  • 17. A coloring depositing shampoo composition for human hair comprising: a cationic dye selected from the group consisting of Basic Blue 124, Basic Yellow 87, Basic Red 51, Basic Orange 31, Basic Brown 17, Basic Blue 99, HC Blue 16, HC Blue 15, Basic Violet 2, Basic Brown 16, and Basic Yellow 57;a nonionic surfactant comprising n-methyl alkyl glucamide with a carbon chain lengths of 8 and 10 selected from the group consisting of capryloyl/caproyl methyl glucamide and cocoyl methyl glucamide; andan aqueous carrier comprising water;wherein said composition comprises, by weight, less than 0.50% cationic dye.
  • 18. The composition of claim 17, further comprising: a stabilizer comprising a combination of Di-t-butyl-4-hydroxyhydrocinnamate and Tris (Tetramethylhydroxypiperidinol) Citrate; anda fragrance.
  • 19. The composition of claim 17, wherein said composition does not contain any anionic surfactant.
  • 20. A method of dyeing human hair, which comprises shampooing the hair with the composition as claimed in claim 1.
  • 21. A method of dyeing human hair, which comprises shampooing the hair with the composition as claimed in claim 13.
  • 22. A method of dyeing human hair, which comprises shampooing the hair with the composition as claimed in claim 17.
CROSS REFERENCE

This application is a continuation-in-part of, and claims the benefit of, U.S. application Ser. No. 15/140,064 filed Apr. 27, 2016, expected to issue as U.S. Pat. No. 9,889,080, which claims the benefit of U.S. Provisional Patent Application No. 62/158,296 filed on May 7, 2015, and also claims the benefit of U.S. Provisional Application Ser. No. 62/546,903 filed on Aug. 17, 2017, each which is expressly incorporated herein in its entirety by reference thereto.

US Referenced Citations (129)
Number Name Date Kind
2338746 Van Riper et al. Jan 1944 A
3033824 Huffman May 1962 A
3706725 Ozutsumi et al. Dec 1972 A
3743662 Eurlings et al. Jul 1973 A
3822247 Ozutsumi et al. Jul 1974 A
3920384 Feinland et al. Nov 1975 A
4172703 Fakhouri Oct 1979 A
4630080 Satake et al. Dec 1986 A
4662892 Pike May 1987 A
4875902 Grollier et al. Oct 1989 A
4900468 Mitchell et al. Feb 1990 A
5032138 Wolfram et al. Jul 1991 A
5067966 Mager et al. Nov 1991 A
5085857 Reid et al. Feb 1992 A
5507063 Hirsch Apr 1996 A
5520707 Lim et al. May 1996 A
5637115 Balzer et al. Jun 1997 A
5643341 Hirsch et al. Jul 1997 A
5733536 Hill et al. Mar 1998 A
5855626 Wiegner et al. Jan 1999 A
5891200 Lim et al. Apr 1999 A
5922310 Chaudhuri et al. Jul 1999 A
5961664 Anderson Oct 1999 A
5981548 Paolini et al. Nov 1999 A
5997764 Ambuter et al. Dec 1999 A
6008359 Jachowicz et al. Dec 1999 A
6083422 Ambuter et al. Jul 2000 A
6231877 Vacher et al. May 2001 B1
6395258 Steer May 2002 B1
6440177 Orr Aug 2002 B1
6475248 Ohashi et al. Nov 2002 B2
6500413 Kapsner et al. Dec 2002 B1
6530959 Lang et al. Mar 2003 B1
6592632 Vainshelboim et al. Jul 2003 B2
6616708 Ohashi et al. Sep 2003 B2
6635262 Jourdan et al. Oct 2003 B2
6699463 Chaudhuri Mar 2004 B2
6746493 Miyabe et al. Jun 2004 B2
6814762 Matsunaga Nov 2004 B2
6878169 Matsunaga Apr 2005 B2
7012048 Drovetskaya et al. Mar 2006 B2
7048770 Azizova et al. May 2006 B2
7056355 Pratt et al. Jun 2006 B2
7087221 Royce et al. Aug 2006 B2
7135168 Miczewski et al. Nov 2006 B2
7172632 Smith et al. Feb 2007 B2
7217752 Schmucker-Castner et al. May 2007 B2
7378479 Tamareselvy et al. May 2008 B2
7494514 Narasimhan et al. Feb 2009 B2
7527653 Azizova et al. May 2009 B2
7528100 Gunn et al. May 2009 B2
7578857 Massoni Aug 2009 B1
7604796 Watanabe Oct 2009 B2
7651538 Yamaguchi et al. Jan 2010 B2
7699897 Nguyen et al. Apr 2010 B2
7736396 Fukuhara et al. Jun 2010 B2
7749284 Lockridge et al. Jul 2010 B2
7758659 Massoni Jul 2010 B2
7824449 Hayama et al. Nov 2010 B2
7857862 Koike et al. Dec 2010 B2
7857863 Koike et al. Dec 2010 B2
7862625 Koike et al. Jan 2011 B2
7985266 Zhang et al. Jul 2011 B2
8118881 Yamaguchi et al. Feb 2012 B2
8207108 Jermann et al. Jun 2012 B2
8227426 Gupta et al. Jul 2012 B2
8298298 Miller Oct 2012 B1
8313537 Xue et al. Nov 2012 B2
8318143 Van Gogh et al. Nov 2012 B2
8343469 Bierganns et al. Jan 2013 B2
8357356 Zaeska et al. Jan 2013 B2
8361167 Blackburn et al. Jan 2013 B2
8394361 Frantz et al. Mar 2013 B1
8394851 Gupta et al. Mar 2013 B2
8440174 Panandiker et al. May 2013 B2
8450294 Lepilleur et al. May 2013 B2
8529637 Vohra et al. Sep 2013 B2
8541325 Duran et al. Sep 2013 B2
8541352 Randall et al. Sep 2013 B2
8637569 Birbara Jan 2014 B2
8663340 Sutton et al. Mar 2014 B2
8673371 Kim et al. Mar 2014 B2
8702814 Sutton et al. Apr 2014 B2
8709100 Sutton et al. Apr 2014 B2
8735533 Hong et al. May 2014 B2
8795644 Tan et al. Aug 2014 B2
8795646 Coore Aug 2014 B2
8802069 Tan et al. Aug 2014 B2
8802070 Tan et al. Aug 2014 B2
8829118 Hessefort et al. Sep 2014 B2
8939158 Mercier et al. Jan 2015 B2
9096882 Meyer et al. Aug 2015 B2
20020015718 Kruse et al. Feb 2002 A1
20020042958 Orr et al. Apr 2002 A1
20020046430 Matsunaga et al. Apr 2002 A1
20030198607 Chaudhuri Oct 2003 A1
20040040095 King et al. Mar 2004 A1
20040244127 Adam et al. Dec 2004 A1
20050011012 Sun et al. Jan 2005 A1
20050112074 Arai et al. May 2005 A1
20060070191 Lang Apr 2006 A1
20060269501 Johnson et al. Nov 2006 A1
20070017039 Errey et al. Jan 2007 A1
20070251029 Bureiko et al. Nov 2007 A1
20070269466 Wakefield et al. Nov 2007 A1
20090068278 Golz-Berner et al. Mar 2009 A1
20090214459 Ascione et al. Aug 2009 A1
20090320215 Massoni Dec 2009 A1
20100064449 Khan et al. Mar 2010 A1
20100125956 Koike et al. May 2010 A1
20100143274 Deshayes et al. Jun 2010 A1
20100158830 Wei et al. Jun 2010 A1
20100197812 Nahas et al. Aug 2010 A1
20110035885 Zhang et al. Feb 2011 A1
20110035886 Zhang et al. Feb 2011 A1
20110236324 Deo Sep 2011 A1
20120171156 Basketter et al. Jul 2012 A1
20120230925 Wagner et al. Sep 2012 A1
20120230968 Worden, Sr. Sep 2012 A1
20120236324 Muraishi Sep 2012 A1
20120276210 Dihora et al. Nov 2012 A1
20130101515 Meyer et al. Apr 2013 A1
20140026332 Jo et al. Jan 2014 A1
20140044762 Colaco et al. Feb 2014 A1
20140193350 Bauer et al. Jul 2014 A1
20140227328 Dihora et al. Aug 2014 A1
20140242018 Zasloff Aug 2014 A1
20140287973 Sivik et al. Sep 2014 A1
20140329428 Glenn, Jr. et al. Nov 2014 A1
Foreign Referenced Citations (20)
Number Date Country
1291468 Apr 2001 CN
101305968 Nov 2008 CN
101357106 Feb 2009 CN
103932967 Jul 2014 CN
103360789 Apr 2015 CN
0137178 Apr 1985 EP
0503507 Sep 1992 EP
0559375 Sep 1993 EP
1153598 Nov 2001 EP
1369105 Dec 2003 EP
1484048 Dec 2004 EP
1915984 Apr 2008 EP
1535599 Jan 2013 EP
WO 2002042380 May 2002 WO
WO 2002051370 Jul 2002 WO
WO 03006554 Jan 2003 WO
WO 200487086 Oct 2004 WO
WO 2008003529 Jan 2008 WO
WO 2008020730 Feb 2008 WO
WO 2014029843 Feb 2014 WO
Non-Patent Literature Citations (2)
Entry
International Search Report dated Aug. 11, 2016 from PCT/US16/31232.
International Search Report dated Sep. 25, 2018 from PCT/US2018/46876.
Related Publications (1)
Number Date Country
20180168976 A1 Jun 2018 US
Provisional Applications (2)
Number Date Country
62158296 May 2015 US
62546903 Aug 2017 US
Continuation in Parts (1)
Number Date Country
Parent 15140064 Apr 2016 US
Child 15894348 US