(en)The present invention is directed to a cosmetic composition comprising an effect pigment based on a glass flake as a substrate with a coating, said coating comprising at least one layer of at least one high refractive material, said material having a refractive index of at least 1.8, and/or a semitransparent metal coating wherein said glass flakes comprising the following composition: 65-75 wt.-% silicon oxide, preferably SiO 2 2-9 wt.-% aluminium oxide, preferably Al 2 O 3 0.0-5 wt.-% calcium oxide, preferably CaO 5-12 wt.-% sodium oxide, preferably Na 2 O 8-15 wt.-% boron oxide, preferably B 2 O 3 0.1-5 wt.-% titanium oxide, preferably TiO 2 0.0-5 wt.-% zirconium oxide, preferably ZrO 2 based on the weight of said glass flakes. The invention is also directed to the use of the cosmetic composition.

1.ApplicationNumber: US-59450908-A
1.PublishNumber: US-8765103-B2
2.Date Publish: 20140701
3.Inventor: KAUPP GÜNTER
SCHMIDT ULRICH
STEINBACH KATRIN
SCHUMACHER DIRK

4.Inventor Harmonized: KAUPP GÜNTER(DE)
SCHMIDT ULRICH(DE)
STEINBACH KATRIN(DE)
SCHUMACHER DIRK(DE)

5.Country: US
6.Claims:
(en)The present invention is directed to a cosmetic composition comprising an effect pigment based on a glass flake as a substrate with a coating, said coating comprising at least one layer of at least one high refractive material, said material having a refractive index of at least 1.8, and/or a semitransparent metal coating wherein said glass flakes comprising the following composition: 65-75 wt.-% silicon oxide, preferably SiO 2 2-9 wt.-% aluminium oxide, preferably Al 2 O 3 0.0-5 wt.-% calcium oxide, preferably CaO 5-12 wt.-% sodium oxide, preferably Na 2 O 8-15 wt.-% boron oxide, preferably B 2 O 3 0.1-5 wt.-% titanium oxide, preferably TiO 2 0.0-5 wt.-% zirconium oxide, preferably ZrO 2 based on the weight of said glass flakes. The invention is also directed to the use of the cosmetic composition.

7.Description:
(en)CROSS REFERENCE TO RELATED APPLICATIONS
The present application is a 35 U.S.C. §371 National Phase conversion of PCT/EP2008/002712, filed Apr. 4, 2008, which claims benefit of European Application No. 07007257.4, filed Apr. 5, 2007, the disclosure of which is incorporated herein by reference. The PCT International Application was published in the English language.
TECHNICAL FIELD
The present invention is directed to a cosmetic composition comprising effect pigments.
BACKGROUND OF THE INVENTION
Pearlescent pigments are increasingly used in cosmetic preparations due to their very decorative optic properties.
EP 0 912 640 B1 discloses a pearlescent pigment comprising flakes of C glass having a first coating comprising iron oxide or rutile titanium dioxide thereon. The skilled person reads from EP 0 912 640 B1 that flakes of C glass are the only glass flakes which allow to produce high quality effect pigments.
The DE 199 07 313 A1 discloses the use of shiny pigments coated with several layers in cosmetics. DE 199 07 313 A1 does not disclose pearlescent pigments based on glass flakes are mentioned.
DE 10 2005 029 647 A1 discloses cosmetic formulations providing a protection against infrared rays. The protection is mainly achieved by pearlescent pigments, which partly reflect infrared radiation. The pearlescent pigments are based on all kinds of common substrates: synthetic or natural mica, SiO 2 -platelets, Al 2 O 3 -platelets, glass flakes or polymer flakes.
Pearlescent pigments based on Al 2 O 3 -platelets, however, are available only in sizes below about 30 μm. Manufactures of pearlescent pigments for the cosmetic market, however, want to offer a product program of various sizes based on a single source of substrate. SiO 2 -flakes are expensive to produce and quite difficult to be produced in constant quality. Furthermore they exhibit extremely high colourflops which are not always demanded. Glass flakes would be the best choice as artificial substrates for effect pigments, especially for pearlescent pigments, because they can be produced reproducibly at fairly low costs and are achievable in various sizes and thicknesses.
In cosmetic formulations there is still a demand for glass flake-based pearlescent pigments with improved skin feeling and higher gloss properties.
SUMMARY:
Therefore, it is an object of this invention to provide a cosmetic formulation containing pearlescent pigments with better skin feeling and higher gloss properties than hitherto used pearlescent pigments based on glass flakes.
The object underlying the present invention is solved by providing a cosmetic composition comprising an effect pigment based on a glass flake as a substrate with a coating, said coating comprising at least one layer of at least one high refractive material, said material having a refractive index of at least 1.8, and/or a semitransparent metal coating wherein said glass flakes comprise the following composition:
65-75 wt.-% silicon oxide, preferably SiO 2 2-9 wt.-% aluminium oxide, preferably Al 2 O 3 0.0-5 wt.-% calcium oxide, preferably CaO 5-12 wt.-% sodium oxide, preferably Na 2 O 8-15 wt.-% boron oxide, preferably B 2 O 3 0.1-5 wt.-% titanium oxide, preferably TiO 2 0.0-5 wt.-% zirconium oxide, preferably ZrO 2 based on the weight of said glass flakes.

For handling effect pigments, for example, during the production of the cosmetic formulations it is desirable that the effect pigments are mechanically stable in order to avoid, e.g., delamination of coated layers.
Surprisingly, the strength of adhesion of the applied layers can be further improved by incorporation of small amounts of titanium oxide, preferably titanium dioxide, into glass compositions used in the production of effect pigments of the present invention. The at least one layer of high refractive material and/or at least one layer of semitransparent metallic material of the effect pigments used in the cosmetic composition of the present invention is firmly adhered to the glass flake containing titanium oxide, preferably titanium dioxide. The content of titanium oxide is preferably in a range of 0.5 to 2.5 wt.-% and more preferably in the range of 1 to 2 wt.-%, based on the weight of said glass flake.
A content above 5 wt.-% of TiO 2 does not further improve the strength of adhesion of subsequent layers in the glass composition as specified in claim 1 . Therefore, further increasing the content of titanium oxide unnecessarily increases the costs and reduces the difference in the index of refraction of the glass substrate and the at least one high refractive index layer and/or semitransparent metallic layer. The larger the difference of the refractive index of the glass flake substrate and of the subsequent layer(s) of high refractive material and/or semitransparent metallic material the stronger are the interference effects of the obtained pearlescent pigments. A stronger interference effect can lead, for example, to a stronger colour flop of the pearlescent pigment.


DETAILED DESCRIPTION
Preferably, said glass composition of the effect pigment comprises a content of titanium oxide of at least 0.5 wt.-%, preferably at least 1 wt.-% of TiO 2 , based on the weight of said glass flake.
Surprisingly, the pearlescent effect pigments used in the present invention do combine the features of a superior mechanical stability and reduced hardness. It is assumed that the reduced hardness is associated with the low contents of aluminium oxide and calcium oxide in the glass composition, respectively.
Most surprisingly, the pearlescent pigments of the present invention have also a softer skin feeling, which renders these pearlescent pigments particular useful as an ingredient for cosmetics.
Preferably, the said glass composition comprises a content of 67-73 wt.-% of silicon oxide, preferably SiO 2 , based on the weight of said glass flake.
Preferably, the said glass composition comprises a content of 4-7 wt.-% of aluminium oxide, preferably Al 2 O 3 , based on the weight of said glass flake.
Preferably, the said glass composition comprises a content of 0.5-2.5 wt.-% and more preferably 1-2.5 wt.-% of calcium oxide, preferably CaO, based on the weight of said glass flake.
Preferably, the said glass composition comprises a content of 8.5-14 wt.-% of boron oxide, preferably B 2 O 3 , more preferably of 9-13 wt.-% of boron oxide, preferably B 2 O 3 , based on the weight of said glass flake.
Preferably, the said glass composition comprises a content of zirconium oxide, preferably ZrO 2 , of 0.05 to 3.0 wt.-%, preferably of 0.1 to 1.5 wt.-%, based on the weight of said glass flake.
Preferably, the said glass composition comprises a content of sodium oxide, preferably Na 2 O, of 6 to 11 wt.-% based on the weight of said glass flake.
In a further embodiment of the said glass composition comprises the following further components:
0 to 6 wt.-%, preferably 1 to 4 wt.-%, potassium oxide and/or lithium oxide, preferably K 2 O and Li 2 O, respectively, and/or 0 to 6 wt.-%, preferably 1.0 to 4.0 wt.-% magnesium oxide, preferably MgO.

The sum of all components of the above glass compositions, including those components not mentioned above do amount in total each to 100 wt.-%.
The glass flake composition used as a substrate for the effect pigments used in the cosmetic composition of the present invention is not a C-glass which is characterised by its superior corrosion resistance. The glass flake composition used as a substrate for the effect pigments used in the cosmetic composition of the present invention is less corrosion resistant than C-glass. Especially in distilled water and in acidic environments the glass flake composition used as substrate in the present invention proved to be less corrosion resistant. In view of EP 0 912 640 B1 teaching that only C-glass flakes can be used for producing pearlescent pigments of high quality it is therefore very surprising that pearlescent pigments of very high optical qualities are obtained with such a glass flake composition having a low corrosion resistance.
Coating of glass flakes with high refractive index materials such as TiO 2 is usually done in aqueous media at ph 1-2 and at elevated temperatures. One would expect that using glass flakes of low corrosion stability under these conditions would lead to a very strong roughening of surface of the glass flake due to dissolution of ions. This would finally lead to a low quality of pearlescent pigments with respect to optical properties like gloss and/or colour flops.
Surprisingly, the present inventors found out that pearlescent pigments with higher gloss can be produced by a glass flake composition of this invention compared to C-glass.
Without being bound to theory it is believed that this unexpected effect is due to a much finer particle size of the coating of the high refractive index material. High refractive index materials, especially metal oxides are well known to be coated in form of oxide grains. Larger grains in the range of more than 50 nm, e.g. more than 75 nm and e.g. more than 100 nm can lead to significant scattering which reduces the gloss of such pearlescent pigments.
It turned surprisingly out that the oxide grains formed on the surface of the glass flakes used in the present invention are very small or fine resulting in a very smooth coating with metal oxide layer(s), such as, e.g., a coating of titanium oxide and/or iron oxide, what in turn results in superior optic properties of the pearlescent pigments of the present invention.
It is currently not understood why glass flakes of the composition of this invention lead to such an effect.
Without being bound to a theory it is currently believed that the lower corrosion resistance compared to the commonly used C-glass of the inventive glassflakes is the reason for this above-mentioned effect. The coating of the high refractive index materials such as TiO 2 occurs at low pH-values of about 1-2. Some metals of the glass flake may be dissolved under these conditions leading to flaws and enhancing the probability to form metal hydroxide and especially silanol functions on the surface of the glass flake. These hydroxide groups can function as excellent binding sites and thus nucleation centers for the precipitating metal oxide precursors. Thus the metal oxide binds better to the glass flakes surface which is very important in the very early stages of the precipitation process. Consequently, the metal oxide can be precipitated in a much finer grain size. Such finer grain sizes of the high refractive index metal oxide in turn lead to lower scattering and thus enhanced gloss and optical properties.
In a further preferred embodiment of the invention the said glass composition has a softening point below 800° C. Such a glass can be produced with less energy costs and hence less total costs. Pursuant to a preferred embodiment of the invention the softening point of the glass composition is in a range of 600° C. to less than 800° C., preferably from 620° C. to 750° C. and further preferred from 650° C. to 700° C.
The inventors of the present invention have realised that the composition of the surface of a glass substrate can have a significant impact on the optical properties of pearlescent pigments using glass flakes as a substrate, in particular if these glass flakes are coated with several layers. Using the effect pigments on the basis of these glass flake substrates in a cosmetic composition enables a superior decorative effect on a substrate, such as hair, skin, fingernail, toenail, etc.
Preferably, the glass flakes containing titanium oxide as a substrate for the effect pigments used in the cosmetic composition of the present invention have a refractive index of less than 1.8. Most preferably the refractive index of the glass flakes is within a range of 1.40 to 1.80, more preferred in a range of 1.45 to 1.7 and mostly preferred in a range of 1.50 to 1.60.
Pursuant to another preferred embodiment of the invention, the difference between the refractive index of the glass flake containing titanium oxide and the subsequently applied layer or layers of high refractive material(s) is at least 0.6, more preferably at least 0.8 and further preferred at least 1.0. According to another preferred embodiment, the difference of the refractive index between the glass flakes substrate and the subsequently applied layer(s) of high refractive material(s) is in a range of 0.9 to 1.3.
When applying titanium dioxide, having a refractive index of 2.7, as a high refractive material on a glass flake having a content of titanium dioxide as specified in claim 1 , it is possible to obtain a difference of refractive index between said glass flake and the subsequently titanium dioxide layer in a range of 0.9 up to 1.3, preferably of 1.0 to 1.2.
According to an embodiment of the invention the effect pigments, used in the cosmetic composition, comprise one or more layers of high refractive material(s), such as metal oxide(s) or metal sulfide(s), which can be coated directly on each other.
The high refractive materials, for example metal oxide(s), metal sulfide(s), have preferably a refractive index of at least 2.0, further preferred of at least 2.2. Pursuant to another embodiment of the invention the refractive index of the high refractive material(s) is at least 2.3. The refractive index can be up to 2.7, 2.9 or 3.5.
For example, a layer of TiO 2 can be directly applied on the surface of the glass flakes containing TiO 2 , followed by a subsequent layer of Fe 2 O 3 , or vice versa. It is, of course, also possible to directly apply a layer composed of a mixture of various high refractive materials such as metal sulfides or metal oxides. A particular useful mixture of metal oxides is a mixture of TiO 2 and Fe 2 O 3 .
According to another embodiment of the invention the layer of high refractive material, e.g. metal oxide and/or metal sulfide, directly applied to the surface of the glass flakes can be doped with tin oxide and/or aluminium oxide. Such doping with tin oxide and/or aluminium oxide may also increase the adhesion between the high refractive material layer on the surface of the glass flakes. When applying an intermediate layer of aluminium oxide or when using aluminium oxide as a doping agent, it is preferred to use aluminium oxide in the boehmite modification.
According to a preferred embodiment of the invention the high refractive material is selected from the group consisting of metal chalcogenides, particularly metal oxides, metal suboxides and metal sulfides, metal oxyhalides, metal nitrides, metal carbides, semitransparent metals and mixtures thereof.
Preferably said high refractive material is preferably selected from the group of metal oxides consisting of titanium dioxide, iron oxides, e.g. hematite, magnetite, goethite, chromium oxide, copper oxide, zinc oxide, tin oxide, vanadium oxide, nickel oxide, antimony oxide, lead oxide, silver oxide, molybdenum oxide, tungsten oxide, zirconium oxide, suboxides and mixtures thereof. Preferred high refractive materials are titanium dioxide and/or iron oxides.
Pursuant to another embodiment of the invention said high refractive material is selected from the group of metal sulfides consisting of titanium sulfide, iron sulfide, chromium sulfide, copper sulfide, zinc sulfide, tin sulfide, nickel sulfide, vanadium sulfide, cobalt sulfide, antimony sulfide, lead sulfide, silver sulfide, lanthanum sulfides, preferably cerium sulphide, molybdenum sulfide, tungsten sulfide, zirconium sulfide, subsulfides and mixtures thereof.
Particularly preferred effect pigments used preferably in the cosmetic composition of the present invention are glass flakes comprised a composition according to claim 1 and comprising or consisting of coatings with the specified high refractive material:
glass flake+TiO 2 layer with TiO 2 being in the rutile modification glass flake+TiO 2 layer with TiO 2 being in the anatase modification glass flake+Fe 2 O 3 layer glass flake+TiO 2 /Fe 2 O 3 layer with TiO 2 being in the rutile modification glass flake+TiO 2 /Fe 2 O 3 layer with TiO 2 being in the anatase modification glass flake+TiO 2 layer+Fe 2 O 3 layer with TiO 2 being in the rutile modification glass flake+TiO 2 layer+Fe 2 O 3 layer with TiO 2 being in the anatase modification glass flake+Fe 2 O 3 layer+TiO 2 layer with TiO 2 being in the rutile modification glass flake+Fe 2 O 3 layer+TiO 2 layer with TiO 2 being in the anatase modification glass flake+TiFe 2 O 5 layer glass flake+Cr 2 O 3 layer glass flake+ZrO 2 layer glass flake+Sn (Sb)O 2 layer glass flake+BiOCl layer glass flake+Al 2 O 3 layer+TiO 2 layer with TiO 2 being in the rutile modification glass flake+SnO 2 layer+TiO 2 layer with TiO 2 being in the rutile modification glass flake+Al 2 O 3 /TiO 2 layer with TiO 2 being in the rutile modification glass flake+SnO 2 /TiO 2 layer with TiO 2 being in the rutile modification glass flake+Ce 2 S 3 layer glass flake+MOS 2 layer

The TiO 2 -coating can exist in the rutile or anatase modification, preferably rutile. In order to apply the titanium dioxide coating in the rutile modification, a precoat consisting of SnO 2 , Al 2 O 3 or Fe 2 O 3 is first applied followed by a subsequent layer of titanium dioxide. The thickness of the precoat SnO 2 or Fe 2 O 3 is preferably <10 nm and most preferably <5 nm.
In addition, layers from Fe 2 O 3 or Fe 2 O 3 /TiO 2 -layers and Cr 2 O 3 are especially preferred as these layers are capable to produce for example skin colour tones, which satisfy decorative demands (bifunctional make-up). Therefore, cosmetic compositions comprising the aforementioned effect pigments are particularly preferred.
Pursuant to another embodiment of the invention the glass flakes can be coated with a semitransparent metal to provide pearlescent effect pigments for use in the cosmetic composition. This said semitransparent metal is selected from the group consisting of aluminium, chromium, silver, gold, copper, titanium, nickel, zinc and mixtures and alloys of these metals. The term “semitransparent” means a transparency of 10 to 90%, preferably of 30 to 70% and most preferably of 40 to 60%, respectively. Thin metal layers of these transparencies are capable to give rise to interference effects with the underlying glass flake substrate. The thickness of these semitransparent metal layers is preferably in a range of between 0.2 nm and 20 nm, preferably between 3 nm and 15 nm.
The semitransparent metal can be coated directly on the glass flake. In this case an interference effect pigment is obtained with a rather metallic appearance.
In another embodiment of the invention this interference pigment, contained in the cosmetic composition of the present invention, can be further coated with high refractive materials.
In another embodiment of the invention the semitransparent metal layer is coated onto a first layer of high refractive index materials.
Particularly preferred effect pigments of the present invention are glass flakes comprised a composition according to claim 1 and comprising or consisting of coatings with the specified semitransparent metals:
glass flake+Al layer glass flake+Ag layer glass flake+TiO 2 layer+Al layer glass flake+TiO 2 layer+Ag layer glass flake+Fe 2 O 3 layer+Al layer glass flake+Fe 2 O 3 layer+Ag layer

The metal layers can be deposited by known methods such as CVD-, PVD-methods or by electroless plating.
In a further preferred embodiment the pearlescent pigments comprise at least one layer of low refractive and at least one layer of high refractive index material.
The low refractive index material refers to materials with a refractive index of <1.8, preferably of <1.7.
Pursuant to another embodiment of the invention the effect pigment comprises a plurality of layers of low refractive and high refractive materials, such as metal oxide(s) and/or metal sulfide(s). According to another embodiment of the invention said layers of low refractive and high refractive materials are alternately arranged on each other.
Especially preferred are alternating layers of high refractive materials with low refractive materials. Such pearlescent pigments are known to exhibit especially strong interference colours. Pearlescent pigments with such alternating layers are, for example, known from the DE 196 18 566 A1, DE 196 38 708, JP 7-246366, EP 1 025 168 A1 or EP 0 753 545 A2.
The at least one layer of low refractive material is selected from the group consisting of low refractive metal oxides, particularly of silica, silica hydrate, silicon oxide hydroxide, silicon oxide hydroxide hydrate, alumina, alumina hydrate, aluminium oxide hydroxide, aluminium oxide hydroxide hydrate, boron oxide, boron hydroxide, magnesium fluoride, magnesium silicate and mixtures thereof.
Examples of suitable metal oxides having a refractive index of more than 1.8 are TiO 2 , Fe 2 O 3 , TiFe 2 O 5 , Ti-suboxides, Fe 3 O 4 , Cr 2 O 3 , ZrO 2 , ZnO, SnO 2 , Sn (Sb)O 2 or mixtures thereof.
The TiO 2 layer can be in the rutile or anatase modification, preferably the TiO 2 layer is rutile. Especially preferred are glass flakes coated with TiO 2 and/or Fe 2 O 3 .
Pursuant to a preferred embodiment the glass flakes are coated preferably with one or more layers of metal oxide selected preferably from the group consisting of TiO 2 , Fe 2 O 3 and mixtures thereof.
Depending on the thickness of the layer(s) of TiO 2 and/or Fe 2 O 3 and the thickness of the low refractive index layer a wide range of colour effects can be produced.
Pursuant to another embodiment of the invention, the one or more metal oxide layers of titanium dioxide is/are in the rutile modification. Rutile has a higher index of refraction compared to anatase and is less photoactive.
If the effect pigments used in the present invention containing TiO 2 in the high refractive index coating are used a subsequent protection coating, e.g., a layer of silicon oxide and/or cerium oxide is preferably applied to suppress the photoactivity, if any. The protection coating can be composed of a first layer of silicon oxide and a second layer of cerium oxide and vice versa, wherein the latter arrangement of layers is particularly preferred.
In a further preferred embodiment the pearlescent pigments are so-called multilayer pigments which comprise the following coatings:
(A) a coating with a refractive index of n>1.8 and an average thickness of 50-350 nm, (B) a coating with a refractive index of n<1.8 and an average thickness of 50-500 nm, (C) a coating with a refractive index of n>1.8 and an average thickness of 20-350 nm.

The thickness of the coatings (A) (B) or (C) can be equal or may differ from each other. Preferably the thickness of the layers (A) and (C) are in the range of 20-350 nm, more preferred 50-250 nm and especially preferred 70-150 nm.
The coating (B) has preferably a thickness of 50-500 nm, more preferred of 100-200 nm and especially preferred 130-180 nm, and is preferably B 2 O 3 , SiO 2 and/or Al 2 O 3 .
The thickness of the coatings (A) und (C) can be equal or may differ from each other. In a most preferable embodiment the coatings (A) und (C) are colourless coatings, especially TiO 2 -coatings. The TiO 2 -coating can exist in the rutile or anatase modification, preferably rutile. In order to apply the titanium dioxide coating in the rutile modification a precoat consisting of SnO 2 , Al 2 O 3 or Fe 2 O 3 can be applied first followed by a subsequent layer of titanium dioxide. The thickness of the precoat SnO 2 or Fe 2 O 3 is preferably <10 nm and most preferably <5 nm.
Particularly preferred multi layer pearlescent pigments used in the cosmetic composition of the present invention are glass flakes comprised of a composition recited claim 1 and comprising or consisting of coatings with the specified high and low refractive materials:
Glass-flake+TiO 2 +SiO 2 +TiO 2 Glass-flake+Fe 2 O 3 +SiO 2 +TiO 2 Glass-flake+TiO 2 +SiO 2 +TiO 2 /Fe 2 O 3 Glass-flake+TiO 2 /Fe 2 O 3 +SiO 2 +TiO 2 /Fe 2 O 3 Glass-flake+TiO 2 /Fe 2 O 3 +SiO 2 +TiO 2 Glass-flake+TiO 2 /Fe 2 O 3 +SiO 2 +Fe 2 O 3 Glass-flake+Fe 2 O 3 +SiO 2 +TiO 2 /Fe 2 O 3 Glass-flake+SiO 2 +TiO 2 +SiO 2 +TiO 2 Glass-flake+SiO 2 +Fe 2 O 3 +SiO 2 +TiO 2 Glass-flake+SiO 2 +TiO 2 +SiO 2 +TiO 2 /Fe 2 O 3 Glass-flake+SiO 2 +TiO 2 /Fe 2 O 3 +SiO 2 +TiO 2 /Fe 2 O 3 Glass-flake+SiO 2 +TiO 2 /Fe 2 O 3 +SiO 2 +TiO 2 Glass-flake+SiO 2 +TiO 2 /Fe 2 O 3 +SiO 2 +Fe 2 O 3 Glass-flake+SiO 2 +Fe 2 O 3 +SiO 2 +TiO 2 /Fe 2 O 3

Glass flakes used in the present invention have a thickness preferably in the range of 0.05 to 10 μm, further preferably of 0.1 μm to 2.0 μm. Pursuant to another embodiment of the invention the thickness of the glass flakes is in a range of 0.05 μm to 1.0 μm, more preferably of 0.1 μm to 0.45 μm.
Very thin glass flakes are preferred, because very brilliant colour effects can be achieved with them. Preferably the glass flakes are produced by methods disclosed in the WO 2004/056716 A1, WO 2005/063637 A1 and the EP 0 289240 A1, which are enclosed by reference therein.
The average particle size of the glass flakes used as a substrate for the effect pigments used in the cosmetic composition in the present invention is preferably in the range of 1 to 1000 μm, more preferably in the range of 5 to 500 μm. Preferred glass flakes have an average particle size in the range of 10 to 200 μm.
The aspect ratio of the glass flakes used as a substrate for the effect pigments used in the cosmetic composition is preferably in the range of 20 to 10,000, preferably in the range of 200 to 3,000. Pursuant to another embodiment of the invention, the aspect ratio is in the range of 300 to 1,500.
If the high refractive index material comprises TiO 2 either alone or in admixture with another compound, such as TiO 2 /Fe 2 O 3 , a subsequent layer of SiO 2 and/or cerium oxide is preferably applied if the photocatalytic activity of the pearlescent pigment is to be isolated from the surrounding. Such protective coatings are described in the DE 10 2004 041 592 A1 and the DE 10 2004 041 586 A1, which are incorporated herein by reference.
It is also possible to additionally include colouring matters such as dyes, colourants, etc. into the layer(s) of high refractive material, such as a metal oxide layer, or a layer of low refractive material, such as a layer of SiO 2 or Al 2 O 3 , or as a separate layer onto the surface of the coating containing the at least one layer of high refractive material. Such colouring matter can be, for example, carmine, Prussian blue (ferric cyanoferrate (II)), carbon black, copper phthalocyanines, diketo pyrrolo pyrrolidones, chinacridones, indolines, isoindolines, azopigments, anthrachinones, FD&C dyes or FD&C lakes.
The surface of the effect pigments used in the present invention may also be organic-chemically modified. Such an organic-chemical surface modification may render the effect pigments a leafing behaviour or a non-leafing behaviour.
Pursuant to a preferred embodiment the glass flakes are coated with at least one layer of a high refractive material and/or a semitransparent metal by wet chemical coating, physical vapour deposition, chemical vapour deposition, or electroless plating.
The glass flakes can be coated in the same way as e.g. mica based pearlescent pigments. Coatings with a metal oxide may be accomplished by any known methods, such as hydrolysis of a metal salt by heating or alkali, which deposits hydrated metal oxide, optionally followed by calcination.
In general, the procedure can involve dispersing of the glass flakes in a suitable solvent, for example organic solvent or water or a water/organic solvent mixture, and combining that dispersion with a precursor which forms a hydrous metal oxide film coating on the flakes. The precursor can be metal salts hydrolysed and subsequently deposited on the glass flake surface.
After the glass flakes are dispersed in water and placed in an appropriate vessel, the appropriate metal salts are added. The pH of the resulting dispersion is maintained at an appropriate level during the addition of the metal salts by simultaneous feeding a suitable base, for example sodium hydroxide, to cause precipitation of the hydrous metal dioxide on the glass flakes. An aqueous acid, for example hydrochloric acid, can be used for adjusting the pH. The coated platelets can, if desired, be washed and dried before being calcined to the final pigment. Appropriate procedures are described in detail in U.S. Pat. No. 5,433,779 and in the German Patents 14 67 468, 19 59 998, 20 09 566, 22 14 545, 22 15 191, 22 44 298, 23 13 331, 25 22 572, 31 37 808, 31 37 809, 31 51 343, 31 51 354, 31 51 355, 3211 602 and 32 53 017 which are incorporated herewith by reference.
Alternatively, alkoxy metal compounds can be dispersed in an organic solvent. The hydrolysis of said alkoxy metal compounds can be started by adding water, for example in an amount of about 1 to 20 wt.-%, preferably 5 to 10 wt.-%, based on the weight of the organic solvent. After hydrolysis of the alkoxy metal compounds, a metal oxide layer is formed on the surface of the glass flakes. As organic solvent preferably alcohols such as ethanol, n-propanol or isopropanol and mixtures thereof can be used.
The effect pigments obtained by wet chemically coating are characterized in that one or more homogeneous layers are enrobing the glass flakes.
The effect pigments used in the cosmetic preparation of the present invention can also be prepared by gas phase decomposition of volatile metal compounds (CVD, PVD) or electroless plating by procedures known in the art.
The cosmetic compositions of this invention can be used in cosmetic formulations in the decorative cosmetics or personal care applications.
The cosmetic composition of the present invention can be prepared by working in the effect pigments into a cosmetic pre-formulation or formulation, for example, by mixing using a stirrer.
The cosmetic compositions according to the invention may also comprise further dyes and coloured pigments. The dyes and coloured pigments can be selected from the corresponding positive list in the German Cosmetics Regulation or the EU list of cosmetic colorants. In most cases, they are identical with the dyes approved for foods. Advantageous coloured pigments are, for example, titanium dioxide, mica, iron oxides (for example Fe 2 O 3 , Fe 3 O 4 , FeO(OH)) and or tin oxide. Advantageous dyes are, for example, carmine, Berlin Blue, Chromium Oxide Green, Ultramarine Blue and or Manganese Violet. It is particularly advantageous to select the dyes and or coloured pigments from the following list. The Colour Index numbers (CINs) are taken from the Rowe Colour Index, 3rd Edition, Society of Dyers and Colourists, Bradford, England, 1971.









Chemical or other name
CIN
Colour



Pigment Green
10006
green

Acid Green 1
10020
green

2,4-Dinitrohydroxynaphthalene-7-sulfonic acid
10316
yellow

Pigment Yellow 1
11680
yellow

Pigment Yellow 3
11710
yellow

Pigment Orange 1
11725
orange

2,4-Dihydroxyazobenzene
11920
orange

Solvent Red 3
12010
red

1-(2′-Ch oro-4′-nitro-1′-phenylazo)-
12085
red

2-hydroxynaphthalene



Pigment Red 3
12120
red

Ceres Red; Sudan Red; Fat Red G
12150
red

Pigment Red 112
12370
red

Pigment Red 7
12420
red

Pigment Brawn 1
12480
brown

N-(5-chloro-2.4-dimethoxyphenyl)-4-
12490
red

[[5-[diethylamino)-sulfonyl]-2-methoxyphenyl]azo]-



3-hydroxynaphthalene-2-carboxamide



Disperse Yellow 16
12700
yellow

1-(4-Sulfo-1-phenylazo)-4-aminobenzene-5-sulfonic
13015
yellow

acid



2,4-Dihydroxy-azobenzene-4′-sulfonic acid
14270
orange

2-(2,4-Dimethylphenylazo-5-sulfonyl)-1-
14700
red

hydroxynaphthalene-4-sulfonic acid



2-(4-Sulfo-1-naphthylazo)-1-aaphthol-4-sulfonic acid
14720
red

2-(6-Sulfo-2,4-xylylazo)-1-naphthol-5-sulfonic acid
14815
red

1-(4′-Sulfophenylazo)-2-hydroxynaphthalene
15510
orange

1-(2-Sulfonyl-4-chloro-5-carboxy-1-phenylazo)-2-
15525
red

hydroxynaphthalene



1-(3-Methylphenylazo-4-sulfonyl)-2-
15580
red

hydroxynaphthalene



(4′,(8′) Sulfonyl)-2-hydroxynaphthalene
15620
red

2-Hydroxy-1,2′-azonaphthalene-1′-sulfonic acid
15630
red

3-Hydroxy-4 phenylazo-2-naphthylcarboxylic acid
15800
red

1-(2-Sulfo-4-methyl-1-phenylazo)-2-
15850
red

naphthylcarboxylic acid



1-(2-Sulfo-4-methyl-5-chloro-1-phenylazo)-
15865
red

2-hydroxy-naphthalene-3-carboxylic acid



1-(2-Sulfo-1-naphthylazo)-2-hydroxynaphthalene-
15880
red

3-carboxylic acid



1-(3-Sulfo-1-phenylazo)-2-naphthol-6-sulfonic acid
15980
orange

1-(4-Sulfo-1-phenylazo)-2-naphthol-6-sulfonic acid
15985
yellow

Allura Red
16035
red

1-(4-Sulfo-1-naphthylazo)-2-naphthol-3,6-
16185
red

sulfonic acid



Acid Orange 10
16230
orange

1-(4-Sulfo-1-naphthylazo)-2-naphthol-6,8-disulfonic
16255
red

acid



1-(4-Sulfo-1-naphthylazo)-2-naphthol-3,6,8-trisulfonic
16290
red

acid



8-Amino-2-phenylazo-1-naphthol-3,6-disulfonic acid
17200
red

Acid Red 1
18050
red

Acid Red 155
18130
red

Acid ellow 121
18690
yellow

Acid Red 180
18736
red

Acid ′Yellow 11
18820
yellow

Acid Yellow 1
18965
yellow

4-(4-Sulfo-1-phenylazo)-1-(4-sulfophenyl)-5-hydroxy-
19140
yellow

pyrazolone-3-carboxylic acid



Pigment Yellow 16
20040
yellow

2,6-(4′-Sulfo-2″,4″-dimethyl)bisphenylazo)-1,3-
20170
orange

Dihydroxy-benzene



Acid Black 1
20470
black

Pigment Yellow 13
21100
yellow

Pigment Yellow 83
21108
yellow

Solvent Yellow
21230
yellow

Acid Red 163
24790
red

Acid Red 73
27290
red

2-[4′-(4″-Sulfo-1″-phenylazo-7-sulfo-1′-
27755
black

naphthylazo]-l-hydroxy-7-aminonaphthalene-3,6-



disulfonic acid



4-[4″-Sulfo-l″-phenylazo)-7′-sulfo-1′-naphlhylazol-
28440
black

l-hydroxy-8-acetylaminonaphthalene-3,5-disulfcnic



acid



Direct Orange 34, 39, 44, 46, 60
40215
orange

Food Yellow
40800
orange

trans-13-Apo-8′-carotene aldehyde (C 30 )
40820
orange

trans-Apo-8′-carolinic acid (C 30 ) ethyl ester
40850
orange

Canthaxanthine
40850
orange

Acid Blue 1
42045
blue

2,4-Disulfo-5-hydroxy-4′-4″-
42051
blue

bis(diethylamino)triphenvlcarbinol



4-[(-4-N-Ethyl-p-sulfobenzylamino)-phenyl-
42053
green

(4-hydroxy-2-sulfophenyl) (methylene)-1-



(N-ethy1-N-p-sulfobenzyl-2,5-cyclohexadienimine]



Acid Blue 7
42080
blue

(N-Ethyl-p-sulfobenzylamino)phenyl-
42090
blue

(2-sulfophenyl)methylene-(N-ethyl-N-p-sulfobenzyl)-



Δ 2,5 -cyclohexadienimine



Acid Green 9
42100
green

Diethyldisulfobenzyldi-4-amino-2-chlorodi-2-
42170
green

methylfuchsonimmonium



Basic Violet 14
42510
violet

Basic Violet 2
42520
violet

2′-Methyl-4′-(N-ethyl-N-m-sulfobenzyl)amino-
42735
blue

4′-(N-diethyl)-amino-2-methyl-N-ethyl-N-m-



sulfobenzylfuchsonimmonium



4′ (N Dimethyl)amino 4″ (N phenyl)aminonaphtho-N-
44045
blue

dimethylfuchsonimnionium



2 Hydroxy 3,6 disulfo 4,4′ bisdimethylamino-
44090
green

naphthofuchsonimmonium



Acid Red 52
45100
red





















































































































It may furthermore be favourable to select, as dye, one or more substances from the following group:
2,4-dihydroxyazobenzene, 1-(2′-chloro-4′-nitro-1′-phenylazo)-2-hydroxynaphthalene, Ceres Red, 2-(4-sulfo-1-naphthylazo)-1-naphthol-4-sulfonic acid, the calcium salt of 2-hydroxy-1,2′-azonaphthalene-1′-sulfonic acid, the calcium and barium salts of 1-(2-sulfo-4-methyl-1-phenylazo)-2-naphthylcarboxylic acid, the calcium salt of 1-(2-sulfo-1-naphthylazo)-2-hydroxynaphthalene-3-carboxylic acid, the aluminium salt of 1-(4-sulfo-1-phenylazo)-2-naphthol-6-sulfonic acid, the aluminium salt of 1-(4-sulfo-1-napthylazo)-2-naphthol-3,6-disulfonic acid, 1-(4-sulfo-1-naphthylazo)-2-naphthol-6,8-disulfonic acid, the aluminium salt of 4-(4-sulfo-1-phenylazo)-2-(4-sulfophenyl)-5-hydroxypyrazolone-3-carboxylic acid, the aluminium and zirconium salts of 4,5-dibromofluorescein, the aluminium and zirconium salts of 2,4,5,7-tetrabromofluorescein, 3′,4′,5′,6′-tetrachloro-2,4,5,7-tetrabromofluorescein and its aluminium salt, the aluminium salt of 2,4,5,7-tetraiodofluorescein, the aluminium salt of quinophthalonedisulfonic acid, the aluminium is salt of indigodisulfonic acid, red and black iron oxide (CIN: 77 491 (red) and 77 499 (black)), iron oxide hydrate (CN: 77492), manganese ammonium diphosphate and titanium dioxide.

Also advantageous are oil-soluble natural dyes, such as, for example, paprika extract, n-carotene or cochineal.
Furthermore, the cosmetic composition of the present invention may include inorganic or organic pigments. Preferably, organic pigments are selected from the group consisting of chinacridones, xanthenes, indigos, cyanines, antocyanes, indanthrenes, isoindolines, monoazo-, bisazo-, trisazopigments, chinolphtalones, anthrachinones, phthalocyanines, carotinoides or mixtures thereof.
Preferred inorganic pigments are selected from the group consisting of TiO 2 , coloured SiO 2 , CaSO 4 , iron oxides, chromium oxides, soot or their mixtures.
The cosmetic composition of the present invention comprise the effect pigments based on the new glass composition described above and dyes or pigments in amounts of 0.5-50 wt.-%; preferably of 1-30 wt.-%; and further preferably of 3-15 wt.-%; based on the total weight of the cosmetic composition, depending on the field of application.
The weight-ratio of the effect pigment to dyes or pigments is preferably 30:1 to 1:10 wt., preferably 20:1 to 1:5, and most preferably 5:1 to 1:5, depending on the field of application.
Also advantageous for the purposes of the present invention are gel creams comprising other pearlescent pigments. Particular preference is given to the types of pearlescent pigment listed below:
1. Natural pearlescent pigments, such as, for example, a) “pearl essence” (guanine hypoxanthine mixed crystals from fish scales) and b) “mother-of-pearl” (ground mussel shells) 2. Monocrystalline pearlescent pigments, such as, for example, bismuth oxychloride (BiOCl)

The effect pigments of the present invention can also be used in the cosmetic preparation in admixture with other coloured or black pearlescent pigments based on metal oxide coated mica, TiO 2 flakes, SiO 2 flakes or Al 2 O 3 flakes and coated or uncoated metal pigments, cholesteric flakes, BiOCl pigments, platelet shaped iron oxides, or graphite flakes.
The cosmetic composition of the present invention can be of any type and be used, for example, for decorative effects on the skin, hair, eyelids, fingernails or toenails, etc. Furthermore, the cosmetic composition or formulation of the present invention may also be combined with other active agents, e.g., pharmaceutically active agents such as dermatologically active agents.
Cosmetic compositions according to the invention or compositions to be used in accordance with the invention may also comprise one or more insect repellents. According to a preferred embodiment of the invention, the at least one repellent is selected from N,N-diethyl-3-methylbenzamide, ethyl 3-(acetylbutylamino)propionate, dimethyl phthalate, butopyronoxyl, 2,3,4,5-bis(2-butylene)tetrahydro-2-furaldehyde, N,N-diethylcaprylamide, N,N-diethylbenzamide, o-chloro-N,N-diethylbenzamide, dimethyl carbate, di-n-propyl isocinchomcronate, 2-ethylhexane-1,3-diol, N-octylbicycloheptenedicarboximide, piperonyl butoxide, 1-(2-methylpropoxycarbonyl)-2-(hydroxyethyl)piperidine, or mixtures thereof, where it is particularly preferably selected from N,N-diethyl-3-methylbenzamide, ethyl 3-(acetylbutylamino)propionate, 1-(2-methylpropoxycarbonyl)-2-(hydroxyethyl)piperidine, octanoic acid, decanoic acid, pyrethrins, pyrethroids, methyl nonyl ketone (undecan-2-one), cycloalkanecarboxylic acids, permethrin and (R)-p-mentha1,8-diol, as well as effective derivatives of the said active ingredients which are known from the literature, or mixtures thereof.
In a preferred embodiment of the present invention, the cosmetic composition may additionally comprise active agents protecting human or animal body cells against oxidative stress, in particular for reducing skin ageing, such as one or more antioxidants.
There are many proven substances which can be used as antioxidants in a cosmetic composition of the present invention, for example amino acids (for example glycine, histidine, tyrosine, tryptophan) and derivatives thereof, imidazoles (for example urocanic acid) and derivatives thereof, peptides, such as D,L-carnosine, D-carnosine, L-carnosine and derivatives thereof (for example anserine), carotinoids, carotenes (for example α-carotene, β-carotene, lycopene) and derivatives thereof, chlorogenic acid and derivatives thereof, lipoic acid and derivatives thereof (for example dihydrolipoic acid), aurothioglucose, propylthiouracil and other thiols (for example thioredoxin, glutathione, cysteine, cystine, cystamine and the glycosyl, N-acetyl, methyl, ethyl, propyl, amyl, butyl and lauryl, palmitoyl, oleyl, γ-linoleyl, cholesteryl and glyceryl esters thereof) and salts thereof, dilauryl thiodipropionate, distearyl thiodipropionate, thiodipropionic acid and derivatives thereof (esters, ethers, peptides, lipids, nucleotides, nucleosides and salts), and sulfoximine compounds (for example buthionine sulfoximines, homocysteine sulfoximine, buthionine sulfones, penta-, hexa- and heptathionine sulfoximine) in very low tolerated doses (for example pmol to μmol/kg), and also (metal) chelating agents (for example α-hydroxy fatty acids, palmitic acid, phytic acid, lactoferrin), α-hydroxy acids (for example citric acid, lactic acid, malic acid), humic acid, bile acid, bile extracts, bilirubin, biliverdin, EDTA, EGTA and derivatives thereof, unsaturated fatty acids and derivatives thereof, vitamin C and derivatives (for example ascorbyl palmitate, magnesium ascorbyl phosphate, ascorbyl acetate), tocopherols and derivatives (for example vitamin E acetate), vitamin A and derivatives (for example vitamin A palmitate), and coniferyl benzoate of benzoin resin, rutinic acid and derivatives thereof, α-glycosyl rutin, ferulic acid, furfurrylideneglucitol, carnosine, butylhydroxytoluene, butylhydroxyanisole, nordihydroguaiaretic acid, trihydroxybutyrophenone, quercetin, uric acid and derivatives thereof, mannose and derivatives thereof, zinc and derivatives thereof (for example ZnO, ZnSO 4 ), selenium and derivatives thereof (for example selenomethionine), stilbenes and derivatives thereof (for example stilbene oxide, trans-stilbene oxide).
Mixtures of antioxidants are likewise suitable for use in the cosmetic compositions according to the invention. Known and commercial mixtures are, for example, mixtures comprising, as active ingredients, lecithin, L-(+)-ascorbyl palmitate and citric acid (for example Oxynex® AP), natural tocopherols, L-(+)-ascorbyl palmitate, L-(+)-ascorbic acid and citric acid (for example Oxynex® K LIQUID), tocopherol extracts from natural sources, L-(+)-ascorbyl palmitate, L-(+)-ascorbic acid and citric acid (for example Oxynex® L LIQUID), DL-α-tocopherol, L-(+)-ascorbyl palmitate, citric acid and lecithin (for example Oxynex® LM) or butylhydroxytoluene (BHT), L-(+)-ascorbyl palmitate and citric acid (for example Oxynex® 2004).
The compositions according to the invention may comprise vitamins as further ingredients. The cosmetic compositions according to the invention preferably comprise vitamins and vitamin derivatives selected from vitamin A, vitamin A propionate, vitamin A palmitate, vitamin A acetate, retinol, vitamin B, thiamine chloride hydrochloride (vitamin B1), riboflavin (vitamin B), nicotinamide, vitamin C (ascorbic acid), vitamin D, ergocalciferol (vitamin D2), vitamin E, DL-α-tocopherol, tocopherol P acetate, tocopherol hydrogensuccinate, vitamin K1, esculin (vitamin P active ingredient), thiamine (vitamin B1), nicotinic acid (niacin), pyridoxine, pyridoxal, pyridoxamine (vitamin BO), pantothenic acid, biotin, folic acid and cobalamine (vitamin B12), particularly preferably vitamin A palmitate, vitamin C and derivatives thereof, DL-α-tocopherol, tocopherol P acetate, nicotinic acid, pantothenic acid and biotin.
Of the phenols having an antioxidative action, the polyphenols, some of which are naturally occurring, are of particular interest for applications in the pharmaceutical, cosmetic or nutrition sector. For example, the flavonoids or bioflavonoids, which are principally known as plant dyes, frequently have an antioxidant potential. K. Lemanska, H. Szymusiak, B. Tyrakowska, R. Zielinski, I. M. C. M. Rietjens; Current Topics in Biophysics 2000, 24 (2), 101-108, are concerned with effects of the substitution pattern of mono- and dihydroxyflavones. It is observed therein that dihydroxyflavones containing an OH group adjacent to the keto function or OH groups in the 3,4′- or 6,7- or 7,8-position have antioxidative properties, while other mono- and dihydroxyflavones in some cases do not have antioxidative properties.
Quercetin (cyanidanol, cyanidenolon 1522, meletin, sophoretin, ericin, 3,3′,4′,5,7-pentahydroxyflavone) is frequently mentioned as a particularly effective antioxidant (for example C. A. Rice-Evans, N.J. Miller, G. Paganga, Trends in Plant Science 1997, 2 (4), 152-159). K. Lemanska, H. Szymusiak, B. Tyrakowska, R. Zielinski, A.
E. M. F. Sollers, I. M. C. M. Rietjens; Free Radical Biology&Medicine 2001, 31 (7), 869-881, have investigated the pH dependence of the antioxidant action of hydroxyflavones. Quercetin exhibits the greatest activity amongst the structures investigated over the entire pH range.
Cosmetic compositions which are particularly preferred in accordance with the invention are those which convey sun protection and preferably also comprise UV filter(s) and/or UV absorber(s).
In principle, all UV filters are suitable for use in the cosmetic composition in accordance with the invention. Particular preference is given to UV filters whose physiological acceptability has already been demonstrated. Both for UVA and UVB filters, there are many proven substances which are known from the specialist literature, for example benzylidenecamphor derivatives, such as
3-(4′-methylbenzylidene)-dl-camphor (for example Eusolex® 6300), 3-benzylidenecamphor (for example Mexoryl® SD), polymers of N-{(2 and 4)-[(2-oxoborn-3-ylidene) m -ethyl]-benzyl}acrylamide (for example Mexoryl® SW), N,N,N-trimethyl-4-(2-oxoborn-3-ylidenemethyl) anilinium methylsulfate (for example Mexoryl® SIC) or (2-oxoborn-3-ylidene)toluene-4-sulfonic acid (for example Mexoryl® SL), benzoyl- or dibenzoylmethanes, such as 1-(4-tert-butylphenyl)-3-(4-methoxyphenyl)propane-1,3-dione (for example Eusolex® 9020) or 4-isopropyldibenzoyl-methane (for example Eusolex® 8020), benzophenones, such as 2-hydroxy-4-methoxybenzophenone (for example Eusolex® 4360) or 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid and its sodium salt (for example Uvinul® MS-40), methoxycinnamic acid esters, such as octyl methoxycinnamate (for example Eusolex® 2292), isopentyl 4-methoxycinnamate, for example as a mixture of the isomers (for example Neo Heliopan® IE 1000), salicylate derivatives, such as 2-ethylhexyl salicylate (for example Eusolex® OS), 4-isopropylbenzyl salicylate (for example Megasol®) or 3,3,5-trimethylcyclohexyl-salicylate (for example Eusolex® HMS), 4-aminobenzoic acid and derivatives, such as 4-aminobenzoic acid, 2-ethylhexyl 4-(dimethylamino)benzoate (for example Eusolex® 6007) or ethoxylated ethyl 4-aminobenzoate (for example Uvinul® P25), phenylbenzimidazolesulfonic acids, such as 2-phenylbenzimidazole-5-sulfonic acid and the potassium, sodium and triethanolamine salts thereof (for example Eusolex® 232), 2,2-(1,4-phenylene)bisbenzimidazole-4,6-disulfonic acid and salts thereof (for example Neoheliopan® AP) or 2,2-(1,4-phenylene)bisbenzimidazole-6-sulfonic acid; and further substances, such as 2-ethylhexyl 2-cyano-3,3-diphenylacrylate (for example Eusolexe OCR), 3,3′-(1,4-phenylenedimethylene)bis(7,7-dimethyl-2-oxobicyclo[2.2.1]-hept-1-ylmethancsulfonic acid and salts thereof (for example Mexoryl® SX), 2,4,6-trianilino-(p-carbo-2′-ethylhexyl-1′-oxy)-1,3,5-triazine (for example Uvinul® T 150) and hexyl 2-(4-diethylamino-2-hydroxybenzoyl-)benzoate (for example Uvinul® UVA Plus, BASF).

The compounds mentioned in the list should only be regarded as examples. It is of course also possible to use other UV filters.
These organic UV filters are preferably incorporated into the formulations in an amount of from 0.5 to 10 percent by weight, preferably 1-8%.
Further suitable organic UV filters are, for example,
2-(2H-benzotriaxol-2-yl)-4-methyl-6-(2-methyl-3-(1,3,3,3-tetra methyl-1-(trimethylsilyloxy)disiloxanyl)propyl)phenol (for example Silatrizole®), 2-ethylhexyl 4,4′-[(6-[4-((1,1-dimethylethyl)aminocarbonyl)phenylamino]-1,3,5-triazine-2,4-diyl-)diimino]bis(benzoate) (for example Uvasorb® HEB), α-(trimethylsilyl)-ω-[trimethylsilyl)oxy]poly[oxy(dimethyl [and approx. 6% of methyl[2-[p-[2,2-bis(ethoxycarbonyl]vinyl]phenoxy]-1-methylenethyl] and approx. 1.5% of methyl[3-[p-[2,2-bis(ethoxycarbonyl)vinyl)phenoxy)propenyl) and 0.1 to 0.4% of (methylhydrogen]silyiene]] (n ≈60) (CAS No. 207 574 74-1), 2,2′-methylenebis(6-(2H-benxotriazol-2-yl)-4-(1,1,3,3-tetramethylbutyl)phenol) (CAS No. 103 597-45-1), 2,2′-(1,4-phenylene)bis( 1 H-benximidaxole-4,6-disulfonic acid, monosodium salt) (CAS No. 180 898-37-7) and 2,4-bis{[4-(2-ethylhexyloxy)-2-hydroxyl]phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (CAS No. 103 597-45-, 187 393-00-6).

Further suitable UV filters are also methoxyflavones corresponding to the earlier German patent application DE-A-10232595.
Organic UV filters are generally incorporated into cosmetic formulations in an amount of from 0.5 to 20 percent by weight, preferably 1-15%.
Conceivable inorganic UV filters are those from the group consisting of the titanium dioxides, such as, for example, coated titanium dioxide (for example Eusolex® 1-2000, Eusolex® 1-AQUA, Eusolex® 1-AVO), zinc oxides (for example Sachtotec®), iron oxides and also cerium oxides. These inorganic UV filters are generally incorporated into cosmetic compositions in an amount of from 0.5 to 20 percent by weight, preferably 2-10%.
Preferred compounds having UV-filtering properties are 3-(4′-methylbenzylidene)-dl-camphor, 1-(4-tert-butylphenyl)-3-(4-methoxyphenyl)propane-1,3-dione, 4-iso-propyldibenzoylmethane, 2-hydroxy-4-methoxybenzophenone, octyl methoxycinnamate, 3,3,5-trimethylcyclohexyl salicylate, 2-ethylhexyl 4-(dimethylamino)benzoate, 2-ethylhexyl 2-cyano-3,3-diphenylacrylate, 2-phenylbenzimidazole-5-sulfonic acid and the potassium, sodium and triethanolamine salts thereof.
The compositions according to the invention containing UV-filter compounds are preferably sun protecting compositions. Such compositions may preferably contain pearlescent pigments according to claim 1 coated with a further protection layer consisting of SiO 2 as described in EP 1 725 301 A1, which is incorporated by reference therein.
The compositions according to the invention may in addition comprise further conventional skin-protecting or skin-care active ingredients. These may in principle be any active ingredients known to the person skilled in the art.
Particularly preferred active ingredients are, for example, also so-called solutes. These are substances which are involved in the osmoregulation of plants or microorganisms and can be isolated from these organisms. The generic term compatible solutes here also encompasses the osmolytes described in German Patent Application DE-A10133202. Suitable osmolytes are, for example, the polyols, methylamine compounds and amino acids and respective precursors thereof. Osmolytes in the sense of German Patent Application DE-A-101 33202 are, in particular, substances from the group consisting of the polyols, such as, for example, myo-inositol, mannitol or sorbitol, and or one or more of the osmolytically active substances mentioned below:
taurine, choline, betaine, phosphorylcholine, glycerophosphorylcholines, glutamine, glycine, α-alanine, glutamate, aspartate and proline. Precursors of these substances are, for example, glucose, glucose polymers, phosphatidylcholine, phosphatidylinositol, inorganic phosphates, proteins, peptides and polyamino acids. Precursors are, for example, compounds which are converted into osmolytes by metabolic steps. Compatible solutes which are preferably employed in accordance with the invention are substances selected from the group consisting of pyrimidinecarboxylic acids (such as ectoin and hydroxyectoin), proline, betaine, glutamine, cyclic diphosphoglycerate, N-acetylornithine, trimethylamine N-oxide, di-myo-inositol phosphate (DIP), cyclic 2,3-diphosphoglycerate (cDPG), 1,1-diglycerol phosphate DGP), 3-mannosyl glycerate (firoin), 3-mannosyl glyceramide (firoin-A) and or dimannosyl diinositol phosphate (DMTP) or an optical isomer, derivative, for example an acid, a salt or ester of these compounds, or combinations thereof.

Of the pyrimidine carboxylic acids, particular mention should be made here of ectoin ((S)-1,4,5,6-tetrahydro-2-methyl-4-pyrimidinecarboxylic acid) and hydroxyectoin ((S,S)-1,4,5,6-tetrahydro-5-hydroxy-2-methyl-4-pyrimidinecarboxylic acid) and derivatives thereof. These compounds stabilise enzymes and other biomolecules in aqueous solutions and organic solvents. Furthermore, they stabilise, in particular, enzymes against denaturing conditions, such as salts, extreme pH values, surfactants, urea, guanidinium chloride and other compounds.
Ectoin and ectoin derivatives, such as hydroxyectoin, can advantageously be used in medicaments. In particular, hydroxyectoin can be employed for the preparation of a medicament for the treatment of skin diseases. Other areas of application of hydroxyectoin and other ectoin derivatives are typically in areas in which, for example, trehalose is used as additive. Thus, ectoin derivatives, such as hydroxyectoin, can be used as protectant in dried yeast and bacteria cells. Pharmaceutical products, such as nonglycosylated, pharmaceutically active peptides and proteins, for example t-PA, can also be protected with ectoin or its derivatives.
In respect of the cosmetic applications, particular mention should be made of the use of ectoin and ectoin derivatives for the care of aged, dry or irritated skin.
Thus, European patent application EP-A-0 671 161 describes, in particular, that ectoin and hydroxyectoin are employed in cosmetic compositions, such as powders, soaps, surfactant-containing cleansing products, lipsticks, rouge, make-up, care creams and sunscreen preparations.
In a further, likewise preferred embodiment of the present invention, the composition according to the invention comprises at least one self-tanning agent.
Advantageous self-tanning agents which can be employed are, inter alia: glycerol aldehyde, hydroxymethylglyoxal, γ-dialdehyde, erythrulose, 6-aldo-D-fructose, ninhydrin, 5-s hydroxy-1,4-naphtoquinone, 2-hydroxy-1,4-naphtoquinone or 1,3-dihydroxyacetone (DHA).
The inventive effect pigments and further active ingredients can be incorporated into cosmetic or dermatological compositions in the customary manner. Suitable compositions are those for external use, for example in the form of a cream, lotion or gel or as a solution which can be sprayed onto the skin. Suitable for internal use are administration forms such as capsules, coated tablets, powders, tablet solutions or solutions.
Use forms of the compositions according to the invention that may be mentioned are, for example, solutions, suspensions, emulsions, PIT emulsions, pastes, ointments, gels, creams, lotions, powders, soaps, surfactant-containing cleansing preparations, oils, aerosols and sprays. Examples of other use forms are sticks, shampoos and shower compositions. Any desired customary carriers, assistants and, if desired, further active ingredients may be added to the composition.
Preferred assistants can be selected from the group consisting of preservatives, antioxidants, stabilisers, solubilisers, vitamins, colorants and odour improvers.
Ointments, pastes, creams and gels may comprise the customary carriers, for example animal and vegetable fats, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silica, talc and zinc oxide, or mixtures of these substances.
Powders and sprays may comprise the customary carriers, for example lactose, talc, silica, aluminium hydroxide, calcium silicate and polyamide powder, or mixtures of these substances. Sprays may additionally comprise the customary propellants, for example chlorofluorocarbons, propane/butane or dimethyl ether.
Solutions and emulsions may comprise the customary carriers, such as solvents, solubilisers and emulsifiers, for example water, ethanol, isopropanol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butyl glycol, oils, in particular cottonseed oil, peanut oil, wheatgerm oil, olive oil, castor oil and sesame oil, glycerol fatty acid esters, polyethylene glycols and fatty acid esters of sorbitan, or mixtures of these substances.
Suspensions may comprise the customary carriers, such as liquid diluents, for example water, ethanol or propylene glycol, suspending agents, for example ethoxylated isostearyl alcohols, polyoxyethylene sorbitol esters and polyoxyethylene sorbitan esters, microcrystalline cellulose, aluminium metahydroxide, bentonite, agar-agar and tragacanth, or mixtures of these substances.
Soaps may comprise the customary carriers, such as alkali metal salts of fatty acids, salts of fatty acid monoesters, fatty acid protein hydrolysates, isothionates, lanolin, fatty alcohol, vegetable oils, plant extracts, glycerol, sugars, or mixtures of these substances. Surfactant-containing cleansing products may comprise the customary carriers, such as salts of fatty alcohol sulfates, fatty alcohol ether sulfates, sulfosuccinic acid monoesters, fatty acid protein hydrolysates, isothionates, imidazolinium derivatives, methyl taurates, sarcosinates, fatty acid amide ether sulfates, ailcylamidobetaines, fatty alcohols, fatty acid glycerides, fatty acid diethanolamides, vegetable and synthetic oils, lanolin derivatives, ethoxylated glycerol fatty acid esters, or mixtures of these substances.
Face and body oils may comprise the customary carriers, such as synthetic oils, such as fatty acid esters, fatty alcohols, silicone oils, natural oils, such as vegetable oils and oily plant extracts, paraffin oils or lanolin oils, or mixtures of these substances.
Further typical cosmetic use forms are body powder, powder make-up, emulsion make-up, wax make-up, eye-shadow, foundation, lip gloss, lip liner, lip-stick, lip-care-stick, liquid eyeliner, mascara, mousse, rouge, hair shampoo, nail polish, eye liner, shower gel, body lotion, sunscreen, pre-sun preparations or after-sun preparation.
The preferred composition forms according to the invention also include, in particular, emulsions. Emulsions according to the invention are advantageous and comprise, for example, the said fats, oils, waxes and other fatty substances, as well as water and an emulsifier, as usually used for a composition of this type.
The lipid phase may advantageously be selected from the following group of substances:
mineral oils, mineral waxes; oils, such as triglycerides of capric or caprylic acid, furthermore natural oils, such as, for example, castor oil; fats, waxes and other natural and synthetic fatty substances, preferably esters of fatty acids with alcohols having a low carbon number, for example with isopropanol, propylene glycol or glycerol, or esters of fatty alcohols with alkanoic acids having a low carbon number or with fatty acids; silicone oils, such as dimethylpolysiloxanes, diethylpolysiloxanes, diphenylpolysiloxanes and mixed forms thereof.

For the purposes of the present invention, the oil phase of the emulsions, oleogels or hydrodispersions or lipodispersions is advantageously selected from the group consisting of esters of saturated and or unsaturated, branched and or unbranched alkanecarboxylic acids having a chain length of from 3 to 30 carbon atoms and saturated and or unsaturated, branched and or unbranched alcohols having a chain length of from 3 to 30 carbon atoms, or from the group consisting of esters of aromatic carboxylic acids and saturated and or unsaturated, branched and or unbranched alcohols having a chain length of from 3 to 30 carbon atoms.
Ester oils of this type can then advantageously be selected from the group consisting of isopropyl myristate, isopropyl palmitate, isopropyl stearate, isopropyl oleate, n-butyl stearate, n-hexyl laurate, n-decyl oleate, isooctyl stearate, isononyl stearate, isononyl isononanoate, 2-ethyl-hexyl palmitate, 2-ethylhexyl laurate, 2-hexyldecyl stearate, 2-octyidodecyl palmitate, oleyl oleate, oleyl erucate, erucyl oleate, erucyl erucate and synthetic, semi-synthetic and natural mixtures of esters of this type, for example jojoba oil.
The oil phase may furthermore advantageously be selected from the group consisting of branched and unbranched hydrocarbons and waxes, silicone oils, dialkyl ethers, or the group consisting of saturated and unsaturated, branched and unbranched alcohols, and fatty acid triglycerides, specifically the triglycerol esters of saturated and or unsaturated, branched and or unbranched alkanecarboxylic acids having a chain length of from 8 to 24, in particular 12 to 18, carbon atoms. The fatty acid triglycerides may advantageously be selected, for example from the group consisting of synthetic, semi-synthetic and natural oils, for example olive oil, sunflower oil, soya oil, peanut oil, rapeseed oil, almond oil, palm oil, coconut oil, palm kernel oil and the like.
Any desired mixtures of oil and wax components of this type may also advantageously be employed for the purposes of the present invention. It may also be advantageous to employ waxes, for example cetyl palmitate, as the only lipid component of the oil phase.
The oil phase is advantageously selected from the group consisting of 2-ethylhexyl isostearate, octyldodecanol, isotridecyl isononanoate, isoeicosane, 2-ethylhexyl cocoate, C 12-15 -alkyl benzoate, caprylic/capric acid triglyceride and dicapryl ether.
Particularly advantageous are mixtures of C 12-15 -alkyl benzoate and 2-ethylhexyl isostearate, mixtures of C 12-15 -alkyl benzoate and isotridecyl isononanoate, as well as mixtures of C 12-15 -alkyl benzoate, 2-ethylhexyl isostearate and isotridecyl isononanoate.
Of the hydrocarbons, paraffin oil, squalane and squalene may advantageously be used for the purposes of the present invention.
Furthermore, the oil phase may also advantageously have a content of cyclic or linear silicone oils or consist entirely of oils of this type, although it is preferred to use an additional content of other oil-phase components in addition to the silicone oil or the silicone oils.
The silicone oil which can be used in accordance with the invention is advantageously cyclomethicone (octamethylcyclotetrasiloxane). However, it is also advantageous for the purposes of the present invention to use other silicone oils, for example hexamethylcyclotrisiloxane, polydimethylsiloxane or poly(methylphenylsiloxane). Also particularly advantageous are mixtures of cyclomethicone and isotridecyl isononanoate and of cyclomethicone and 2-ethylhexyl isostearate.
The aqueous phase of the compositions according to the invention optionally advantageously comprises alcohols, diols or polyols having a low carbon number, and ethers thereof, preferably ethanol, isopropanol, propylene glycol, glycerol, ethylene glycol, ethylene glycol monoethyl or monobutyl ether, propylene glycol monomethyl, mono-ethyl or monobutyl ether, diethylene glycol monomethyl or monoethyl ether and analogous products, furthermore alcohols having a low carbon number, for example ethanol, isopropanol, 1,2-propanediol or glycerol, and, in particular, one or more thickeners, which may advantageously be selected from the group consisting of silicon dioxide, aluminium silicates, polysaccharides and derivatives thereof, for example hyaluronic acid, xanthan gum, hydroxypropylmethylcellulose, particularly advantageously from the group consisting of the polyacrylates, preferably a polyacrylate from the group consisting of the so-called Carbopols, for example Carbopol grades 980, 981, 1382, 2984 or 5984, in each case individually or in combination.
In particular, mixtures of the above-mentioned solvents are used. In the case of alcoholic solvents, water may be a further constituent.
Emulsions according to the invention are advantageous and comprise, for example, the said fats, oils, waxes and other fatty substances, as well as water and an emulsifier, as usually used for a formulation of this type.
In a preferred embodiment, the compositions according to the invention comprise hydrophilic surfactants. The hydrophilic surfactants are preferably selected from the group consisting of the alkylglucosides, acyllactylates, betaines and coconut amphoacetates.
It is likewise advantageous to employ natural or synthetic raw materials and assistants or mixtures which are distinguished by an effective content of the active ingredients used in accordance with the invention, for example Plantaren® 1200 (Henkel KGaA), Oramix® NS 10 (Seppic).
A preferred example for a acyllactylates is sodium isostearyl lactylate, for example the product Pathionic® ISL from the American Ingredients Company.
A preferred example for a betaine is capramidopropylbetaine, for example the product lego® Betain 810 from Th. Goldschmidt AG.
A coconut amphoacetate which is advantageous for the purposes of the invention is, for example, sodium coconut amphoacetate, as available under the name Miranole Ultra C32 from Miranol Chemical Corp.
The compositions according to the invention are advantageously characterised in that the hydrophilic surfactant(s) is (are) present in concentrations of 0.01-20% by weight, preferably 0.05-10% by weight, particularly preferably 0.1-5% by weight, in each case based on the total weight of the composition.
For use, the cosmetic and dermatological compositions are applied in sufficient amount to the skin and or hair in the usual manner for cosmetics.
Cosmetic and dermatological compositions according to the invention may exist in various forms. Thus, they may be, for example, a solution, a water-free composition, an emulsion or microemulsion of the water-in-oil (W/O) or oil-in-water (O/W) type, a multiple emulsion, for example of the water-in-oil-in-water (W/O/W) type, a gel, a solid stick, an ointment or an aerosol. It is also advantageous to administer ectoin in encapsulated form, for example in collagen matrices and other conventional encapsulation materials, for example as cellulose encapsulations, in gelatine, wax matrices or liposomally encapsulated. In particular, wax matrices, as described in DE-A 43 08 282, have proven favourable. Preference is given to emulsions. O/W emulsions are particularly preferred. Emulsions, W/O emulsions and O/W emulsions are obtainable in a conventional manner. Emulsifiers that can be used are, for example, the known W/O and O/W emulsifiers. It is advantageous to use further conventional co-emulsifiers in the preferred O/w emulsions according to the invention.
Co-emulsifiers which are advantageous according to the invention are, for example, 0/w emulsifiers, principally from the group consisting of the substances having HLB values of 11-16, very particularly advantageously having HLB values of 14.5-15.5, so long as the O/w emulsifiers have saturated radicals R and R′. If the O/W emulsifiers have unsaturated radicals R and/or R′ or in the case of isoalkyl derivatives, the preferred HLB value of such emulsifiers may also be lower or higher.
It is advantageous to select the fatty alcohol ethoxylates from the group consisting of ethoxylated stearyl alcohols, cetyl alcohols, cetylstearyl alcohols (cetearyl alcohols). Particular preference is given to the following: polyethylene glycol (13) stearyl ether (steareth-13), polyethylene glycol (14) stearyl ether (steareth-14), polyethylene glycol (15) stearyl ether (steareth-15), polyethylene glycol (16) stearyl ether (steareth-16), polyethylene glycol (17) stearyl ether (steareth-17), polyethylene glycol (18) stearyl ether (steareth-18), polyethylene glycol (19) stearyl ether (steareth-19), polyethylene glycol (20) stearyl ether (steareth20), polyethylene glycol (12) isostearyl ether (isostearethy12), polyethylene glycol (13) isostearyl ether (isostearethy13), polyethylene glycol (14) isostearyl ether (isosteareth14), polyethylene glycol (15) isostearyl ether (isosteareth15), polyethylene glycol (16) isostearyl ether (isosteareth16), polyethylene glycol (17) isostearyl ether (isosteareth17), polyethylene glycol (18) isostearyl ether (isosteareth18), polyethylene glycol (19) isostearyl ether (isosteareth19), polyethylene glycol (20) isostearyl ether (isosteareth20), polyethylene glycol (13) cetyl ether (ceteth-13), polyethylene glycol (14) cetyl ether (ceteth-14), polyethylene glycol (15) cetyl ether (ceteth-15), polyethylene glycol (16) cetyl ether (ceteth-16), polyethylene glycol (17) cetyl ether (ceteth-17), polyethylene glycol (18) cetyl ether (ceteth-18), polyethylene glycol (19) cetyl ether (ceteth-19), polyethylene glycol (20) cetyl ether (ceteth-20), polyethylene glycol (13) isocetyl ether (isoceteth-13), polyethylene glycol (14) isocetyl ether (isoceteth-14), polyethylene glycol (15) isocetyl ether (isoceteth-15), polyethylene glycol (16) isocetyl ether (isoceteth-16), polyethylene glycol (17) isocetyl ether (isoceteth-17), polyethylene glycol (18) isocetyl ether (isoceteth-18), polyethylene glycol (19) isocetyl ether (isoceteth-19), polyethylene glycol (20) isocetyl ether (isoceteth-20), polyethylene glycol (12) oleyl ether (oleth-12), polyethylene glycol (13) oleyl ether (oleth-13), polyethylene glycol (14) oleyl ether (oleth-14), polyethylene glycol (15) oleyl ether (oleth-15), polyethylene glycol (12) lauryl ether (laureth-12), polyethylene glycol (12) isolauryl ether (isolaureth-12), polyethylene glycol (13) cetylstcaryl ether (ceteareth-13), polyethylene glycol (14) cetylstearyl ether (ceteareth-14), polyethylene glycol (15) cetylstearyl ether (ceteareth-15), polyethylene glycol (16) cetylstearyl ether (ceteareth-16), polyethylene glycol (17) cetylstearyl ether (ceteareth-17), polyethylene glycol (18) cetylstearyl ether (ceteareth-18), polyethylene glycol (19) cetylstearyl ether (ceteareth-19), polyethylene glycol (20) cetylstearyl ether (ceteareth-20).
It is furthermore advantageous to select the fatty acid ethoxylates from the following group: polyethylene glycol (20) stearate, polyethylene glycol (21) stearate, polyethylene glycol (22) stearate, polyethylene glycol (23) stearate, polyethylene glycol (24) stearate, polyethylene glycol (25) stearate, polyethylene glycol (12) isostearate, polyethylene glycol (13) isostearate, polyethylene glycol (14) isostearate, polyethylene glycol (15) isostearate, polyethylene glycol (16) isostearate, polyethylene glycol (17) isostearate, polyethylene glycol (113) isostearate, polyethylene glycol (19) isostearate, polyethylene glycol (20) isostearate, polyethylene glycol (21) isostearate, polyethylene glycol (22) isostearate, polyethylene glycol (23) isostearate, polyethylene glycol (24) isostearate, polyethylene glycol (25) isostearate, polyethylene glycol (12) oleate, polyethylene glycol (13) oleate, polyethylene glycol (14) oleate, polyethylene glycol (15) oleate, polyethylene glycol (16) oleate, polyethylene glycol (17) oleate, polyethylene glycol (18) oleate, polyethylene glycol (19) oleate, polyethylene glycol (20) oleate.
An ethoxylated alkyl ether carboxylic acid or salt thereof which can advantageously be used is sodium laureth-11 carboxylate. An alkyl ether sulfate which can advantageously be used is sodium laureth-14 sulfate. An ethoxylated cholesterol derivative which can advantageously be used is polyethylene glycol (30) cholesteryl ether. Polyethylene glycol (25) soyasterol has also proven successful. Ethoxylated triglycerides which can advantageously be used are the polyethylene glycol (60) evening primrose glycerides.
It is furthermore advantageous to select the polyethylene glycol glycerol fatty acid esters from the group consisting of polyethylene glycol (20) glyceryl laurate, polyethylene glycol (21) glyceryl laurate, polyethylene glycol (22) glyceryl laurate, polyethylene glycol (23) glyceryl laurate, polyethylene glycol (6) glyceryl caprate capririate, polyethylene glycol (20) glyceryl oleate, polyethylene glycol (20) glyceryl isostearate, polyethylene glycol (18) glyceryl oleate cocoate.
It is likewise favourable to select the sorbitan esters from the group consisting of polyethylene glycol (20) sorbitan monolaurate, polyethylene glycol (20) sorbitan munostearate, polyethylene glycul (20) surbitan munuisustearate, polyethylene glycol (20) sorbitan monopalmitate, polyethylene glycol (20) sorbitan monooleate.
Optional W/O emulsifiers, but ones which may nevertheless be advantageous for the purposes of the invention can be the following:
fatty alcohols having from 8 to 30 carbon atoms, monoglycerol esters of saturated and or unsaturated, branched and or unbranched alkanecarboxylic acids having a chain length of from 8 to 24 carbon atoms, in particular 12-18 carbon atoms, diglycerol esters of saturated and or unsaturated, branched and or unbranched alkanecarboxylic acids having a chain length of from 8 to 24 carbon atoms, in particular 12-18 carbon atoms, monoglycerol ethers of saturated and or unsaturated, branched and or unbranched alcohols having a chain length of from 8 to 24 carbon atoms, in particular 12-18 carbon atoms, diglycerol ethers of saturated and or unsaturated, branched and or unbranched alcohols having a chain length of from 8 to 24 carbon atoms, in particular 12-18 carbon atoms, propylene glycol esters of saturated and or unsaturated, branched and or unbranched ailcanecarboxylic acids having a chain length of from 8 to 24 carbon atoms, in particular 12-18 carbon atoms, and sorbitan esters of saturated and or unsaturated, branched and or unbranched alkanecarboxylic acids having a chain length of from 8 to 24 carbon atoms, in particular 12-18 carbon atoms.

Particularly advantageous W/O emulsifiers are glyceryl monostearate, glyceryl monoisostearate, glyceryl monomyristate, glyceryl monooleate, diglyceryl monostearate, diglyceryl monoisostearate, propylene glycol monostearate, propylene glycol monoisostearate, propylene glycol monocaprylate, propylene glycol monolaurate, sorbitan monoisostearate, sorbitan monolaurate, sorbitan monocaprylate, sorbitan monoisooleate, sucrose distearate, cetyl alcohol, stearyl alcohol, arachidyl alcohol, behenyl alcohol, isobehenyl alcohol, selachyl alcohol, chimyl alcohol, polyethylene glycol (2) stearyl ether (steareth-2), glyceryl monolaurate, glyceryl monocaprinate and glyceryl monocaprylate.
Preferred compositions according to the invention are particularly suitable for protecting human skin against ageing processes and against oxidative stress, i.e. against damage by free radicals, as are produced, for example, by sunlight, heat or other influences. In this connection, they are in the various administration forms usually used for this application. For example, they may, in particular, be in the form of a lotion or emulsion, such as in the form of a cream or milk (O/W, W/O, O/W/O, W/O/W), in the form of oily-alcoholic, oily-aqueous or aqueous-alcoholic gels or solutions, in the form of solid sticks or may be formulated as an aerosol.
The composition may comprise cosmetic adjuvants which are usually used in this type of composition, such as, for example, thickeners, softeners, moisturisers, surfactants, emulsifiers, preservatives, antifoams, perfumes, waxes, lanolin, propellants, dyes and or pigments which colour the composition itself or the skin, and other ingredients usually used in cosmetics.
The dispersant or solubiliser used can be an oil, wax or other fatty substance, a lower monoalcohol or lower polyol or mixtures thereof. Particularly preferred monoalcohols or polyols include ethanol, isopropanol, propylene glycol, glycerol and sorbitol.
A preferred embodiment of the invention is an emulsion in the form of a protective cream or milk which comprises, for example, fatty alcohols, fatty acids, fatty acid esters, in particular triglycerides of fatty acids, lanolin, natural and synthetic oils or waxes and emulsifiers in the presence of water.
Further preferred embodiments are oily lotions based on natural or synthetic oils and waxes, lanolin, fatty acid esters, in particular triglycerides of fatty acids, or oily-alcoholic lotions based on a lower alcohol, such as ethanol, or a glycerol, such as propylene glycol, and or a polyol, such as glycerol, and oils, waxes and fatty acid esters, such as triglycerides of fatty acids.
The composition according to the invention may also be in the form of an alcoholic gel which comprises one or more lower alcohols or polyols, such as ethanol, propylene glycol or glycerol, and a thickener, such as siliceous earth. The oily-alcoholic gels also comprise natural or synthetic oil or wax.
The solid sticks consist of natural or synthetic waxes and oils, fatty alcohols, fatty acids, fatty acid esters, lanolin and other fatty substances.
If a composition is formulated as an aerosol, the customary propellants, such as alkanes, fluoroalkanes and chlorofluoroalkanes, are generally used.
The cosmetic composition may also be used to protect the hair against photochemical damage in order to prevent changes of colour shade, bleaching or damage of a mechanical nature. In this case, a suitable formulation is in the form of a rinse-out shampoo, lotion, gel or emulsion, the composition in question being applied before or after shampooing, before or after colouring or bleaching or before or after permanent waving. It is also possible to select a composition in the form of a lotion or gel for styling or treating the hair, in the form of a lotion or gel for brushing or blow-waving, in the form of a hair lacquer, permanent waving composition, colorant or bleach for the hair. The composition may comprise various adjuvants used in this type of composition, such as surfactants, thickeners, polymers, softeners, preservatives, foam stabilisers, electrolytes, organic solvents, silicone derivatives, oils, waxes, antigrease agents, dyes and or pigments which colour the composition itself or the hair, or other ingredients usually used for hair care.
The compositions according to the invention can be prepared here with the aid of techniques which are well known to the person skilled in the art.
If the inventive cosmetic composition including the new pearlescent pigments used in accordance with the invention are films, a preferred use is the use thereof as or in artificial nails. The present application therefore furthermore relates to an artificial nail comprising the pearlescent pigments based on a new glass flake composition.
Thus, for example, a film comprising the effect pigments based on a new glass flake composition can, after cutting to match the size of the individual fingernail or toenail, be detached from the support sheet and applied to the fingernail toenail and subsequently fixed using clear nail varnish. Alternatively, the films may themselves be provided with an adhesive layer, so that subsequent varnishing is unnecessary. Placing of the film in a varnish before application to the fingernail is also a variant of the present invention in which subsequent varnishing is unnecessary.
Furthermore, the effect pigments based on a new glass flake composition can also be employed in a cosmetic composition like varnishes, such as UV-curable acrylic varnishes, which are used for the production of artificial nails.
A further use of the effect pigments based on a new glass flake composition which is preferred in accordance with the invention is use in nail-care compositions, in particular nail varnishes.
Nail-care compositions, in particular in the form of nail varnishes, are amongst the most-used decorative cosmetic compositions. They usually comprise a synthetic resin as film former and inorganic or organic pigments or dyes. The nail varnishes are intended to exhibit high gloss, high hardness and good adhesion to keratin-containing substances, such as fingernails, and to dry rapidly at room temperature to give a non-tacky, uniform film. The high gloss and the good adhesion should be retained over the longest possible period. In order that the nail varnishes can be removed again using conventional nail varnish removers, the film-forming resins used must be soluble in water acetone mixtures. By contrast, the film-forming resins should be insoluble in water or water alcohol mixtures in order that the nail varnish is not dissolved on contact with water or during handling of conventional household chemicals.
Typical nail varnishes which are suitable for use in accordance with the invention essentially consist of solutions, suspensions or emulsions of certain substances. Particular mention should be made here of binders, such as nitrocellulose, or various synthetic resins, such as, in particular, polyacrylates, polymethacrylates, toluenesulfonamide-formaldehyde resins, toluenesulfonamide-epoxy resins, alkyd resins or polyvinyl acetate. Furthermore, nail varnishes usually comprise suitable solvents for the binders, with solvent mixtures usually being employed. Typical solvents, besides water, are alcohols, esters and ketones, such as, in particular, methyl, ethyl, propyl and butyl acetate, isopropyl alcohol and n-butyl alcohol. The nail varnishes may optionally be provided with further additives for forming the optical appearance, for example soluble dyes. In addition, the mixture may comprise plasticisers (such as, for example, camphor or dibutyl phthalate) and extenders (for example toluene or xylene). These nail varnishes cure through evaporation of the solvent and the other volatile constituents as a function of the layer thickness of the varnish, the temperature and the type of solvent. In addition, the curing time is also dependent on other influences (for example air flow).
Particular preference is given in accordance with the invention to water-based nail-care compositions which preferably comprise polyurethanes or polyacrylates as binder.
Besides water, water-based nail varnishes comprise water-soluble resins, such as, for example, polyurethane resins, acrylic resins, alkyd resins, epoxy resins or melamine resins. The resin here is preferably selected in such a way that it is water-soluble, appears white or transparent in water, is inexpensive and simple to process, is as far as possible non-combustible and is not toxic or hyperallergenic. It may furthermore be essential that the varnish dries rapidly and has good film-forming properties at temperatures from 10° C.
The cosmetic formulations of the present inventions can further comprise antistatic substances, fillers, binders, chelating agents, wetting agents, bleaching agents, cosmetic oils, tensides, odor agents, flavour additives, reduction agents, opacifiers or viscosity regulation agents.
The cosmetic formulations of the present invention consist preferably a body powder, face powder, pressed powder, loose powder, face make-up such as tinted day cream, powder cream, cream make up, powder make-up, emulsion make-up, wax make-up, foundation, mousse, rouge or blush, eye make-up such as eye shadow, mascara, eyeliner, liquid eyeliner, eyebrow pencil, lip care preparation, lipstick, lip gloss, lip liner, hair care preparation such as hair shampoo, rinse-off or leave-on hair conditioner, perm, hair setting preparation, hair fixatives such as hair spray, hair mousse, hair gel, hair wax, permanent or semi-permanent hair dye, temporary hair dye, skin care preparation such as body lotion, body cream, face lotion, face cream, gel, sun care preparation such as sunscreen, pre-sun preparations or after-sun preparation, insect repellent, self tanning preparation, nail polish, skin cleansing preparation such as shower gel, face cleansing preparation or face peeling.
Even without further comments, it is assumed that a person skilled in the art will be able to utilise the above description in its broadest scope. The preferred embodiments should therefore merely be regarded as descriptive disclosure which is absolutely not limiting in any way. The complete disclosure content of all applications and publications mentioned above and below is incorporated into this application by way of reference. The following examples are intended to illustrate the present invention. However, they should in no way be regarded as limiting. All compounds or components which can be used in the compositions are either known and commercially available or can be synthesised by known methods.
EXAMPLES
I Preparations of Pearlescent Pigments
Example 1
200 g of glass flakes (supplied by Glassflakes Ltd. Forster Street Leeds LS10 1PW, United Kingdom) having a composition as specified in Table A with a mean particle thickness of 1 μm and particle diameters in the range of 50-150 μm and a d 50 of 88 μm were dispersed in 2 l of de-ionized water and the suspension was heated up 80° C. under turbulent stirring. Subsequently, the pH was adjusted to 1.9 using diluted hydrochloric acid and an acidic solution of 3 g SnCl 4 *5H 2 O in 60 ml of diluted hydrochloric acid was added to the suspension within 60 minutes. Simultaneously, a solution of sodium hydroxide (10% W/W in water) was metered in order to keep a constant pH of 1.9. After the addition of the tin compound, the reaction mixture was stirred for 15 min to complete the precipitation. Then, the pH is lowered to 1.6 using diluted hydrochloric acid and a solution of TiCl 4 in water (400 g TiCl 4 /l) was added to the suspension with 0.33 ml/min. The pH value was kept constant at 1.6 by co-dosage of sodium hydroxid (10% WAN in water). After 4 h a brilliant silver tone was achieved. The addition of the TiCl 4 solution was stopped and the reaction mixture was stirred for additional 15 minutes. After separation of the solids by filtration, the filter cake was washed using de-ionized water and calcined for 30 minutes at 650° C.
A highly brilliant pearlescent pigment with silver-white reflection colour is obtained. According to X-ray powder diffractometric analysis, the crystal modification of the TiO 2 is pure rutile.





TABLE A



* Composition (X-ray analysis):










SiO 2 :
68.6 wt.-%


Al 2 O 3 :
4.1 wt.-%


CaO:
1.8 wt.-%


MgO:
1.2 wt.-%


K 2 O:
2.0 wt.-%


Na 2 O:
10 wt.-%


B 2 O 3 :
9.9 wt.-%


TiO 2 :
1.6 wt.-%


ZrO 2 :
0.1 wt.-%





























Comparative Example 2
The same procedure as in example 1 was repeated using glass flakes of an ECR-Glass composition having a composition as specified in Table B with the same particle sizes of 50-150 μm and a d 50 of 87 μm.





TABLE B



Composition according to manufacturer (Glassflakes Ltd.

Forster Street Leeds LS10 1PW, United Kingdom):










SiO 2 :
64-70 wt.-%


Al 2 O 3 :
3-6 wt.-%


CaO:
3-7 wt.-%


MgO:
1-4 wt.-%


K 2 O:
0-3 wt.-%


Na 2 O:
12-13 wt.-%


B 2 O 3 :
2-5 wt.-%


TiO 2 :
0-3 wt.-%


ZrO 2 :
—


ZnO:
1-5 wt.-%































Example 3
Analogous to example 1, but the TiCl 4 -solution was added for 23 h with 0.33 ml/min leading to a pearlescent pigment with intensive red interference color.
Comparative Example 4
Commercially available pearlescent pigment Reflecks Sparkling Red (BASF-Catalysts).
Comparative Example 5
Commercially available pearlescent pigment Miraval 5422 Magic Red (MERCK).
The pigments of examples 1 and 3 and of comparative examples 2, 4 and 5 were mixed into conventional nitrocellulose laquer (Erco Bronzelack, Dr. Renger, Germany) and draw-downs on contrast paper were made. The gloss was measured at 60° using a Micro-Tri-Gloss (Byk-Gardner) instrument. The results are shown in table 1.







TABLE 1




Gloss (60°),
Gloss (60°),

Sample
black background
white background



Example 1
102.5 (±1.2)
105.5 (±0.2)

Comparative example 2
95.5 (±0.2)
100.5 (±0.6)

Example 3
79.9
—

Comparative example 4
65.0
—

Comparative example 5
58.4
—






















The gloss of the pearlescent pigment of example 1 is significantly higher than the comparative example 2. Both samples exhibit a silver interference color and similar particle size, particle size distribution and thicknesses.
Within the red interference color pigments of example 3 and comparative examples 4 and 5 the inventive pigment exhibits also a higher gloss than the pigments of the state of the art. The differences in the gloss are even more pronounced compared to the silver pigments.
Example 6
The early stages of precipitation of SnO 2 and of TiO 2 were analysed. For this purpose, example 1 was essentially repeated, however small samples of coated glass flakes were taken at defined reaction times of the reaction mixture (Table 1). The coating with TiO 2 was finally stopped already at 2 hours.
The samples were dried under vacuum at 60° C. The last sample was calcined for 30 minutes at 650° C.
The surface of the samples were analysed by SEM at different magnifications.
Comparative Example 7
Comparative Example 7 was essentially repeated using the glass flakes of an ECR-Glass of comparative example 2 as substrate and samples were taken out at the same reaction times like in example 6. These samples were dried and then analyzed by SEM.





TABLE 2



Reaction stages and times of samples taken of





Sample
Reaction stage and time
Reaction stage and time

number
Example 6
Comparative example 7



a
SnO 2 coating/
SnO 2 coating/


15 min
15 min

b
TiO 2 coating
TiO 2 coating


5 min
5 min

c
TiO 2 coating
TiO 2 coating


5 min
5 min

d
TiO 2 coating
TiO 2 coating


15 min
15 min

e
TiO 2 coating
TiO 2 coating


30 min
30 min

f
TiO 2 coating
TiO 2 coating


60 min
60 min

g
TiO 2 coating
TiO 2 coating


120 min
120 min



































In FIG. 1 a,b the SEM pictures of selected samples of example 6 and comparative example 7, compiled in Table 2, are compared. It can be clearly seen that at the very early stages of coating the glass flakes with metal oxides, e.g. 15 min after SnO 2 coating and 5 min after TiO 2 coating ( FIG. 1 a ), the oxide grains of example 6 are much smaller compared with comparative example 7. In FIG. 1 b one can depict that the oxide grains grow larger in the course of further coating. However, the oxide grains for example 6 remain always significantly smaller compared to the ones of comparative example 7. Even after calcining (sample g) the difference remains. Consequently, even recrystallisation processes of the TiO 2 layers which might occur at calcining do not affect the differences in the dimensions of the oxide grains which existed already before. In sample g a lot of oxide grains with sizes in the 100 nm range and larger can be observed for comparative example 6. Such particles do already significantly reduce the gloss of this pigment. Sample g of example 6, however, doesn't show such large oxide particles.
It is noted, that sample g corresponds to samples which were coated with titania for 2 hours. A silver tone is achieved at 4 hours coating time, however. Thus sample g represents a “pre-silver” pearlescent pigment. Silver is known to be the first colour tone of the interference series followed by gold, red, blue, green and than the second order colours. Consequently, these coloured pearl pigments will exhibit even larger oxide grains and gloss-reducing scattering effects will also increase. Thus the benefits of the smaller oxide grains of the inventive pearlescent pigments will accordingly increase at larger metal oxide thickness.
II Tests Regarding Skin Feeling
IIa Triangular Test
Comparative Example 8
Commercially available Firemist Blue (Pearlescent pigment from BASF Catalysts) for cosmetic use.
The pigments of example 1 and of comparative example 8 were compared in a triangular test. This test is designated to show whether two pigments exhibit a difference in skin feeling.
Procedure:
Three coded samples of the two different pigments where applied on the forearm of the panellist. The panellists arms where placed in a box to prevent the panellist from looking at the arms. Two of the samples are the same, one sample is different. The panellist was asked to touch the samples and to answer the following question:
Which two samples are similar?
Result:
11 out of 20 panellist answered correctly.
This shows that the samples of example 1 and of comparative example 8 are significantly different (based on a significance level of α=0.05)
IIb Panel Tests Skin Feeling
Panel tests regarding the skin feeling have conducted with the pigments of example 1 and comparative example 2.
Procedure:
Two coded samples where applied on the forearm of the panellist. The panellists arms where placed in a box to prevent the panellist from looking at the arms. The panellist was asked to touch the samples and to compare the two samples in regards to the parameter “smoothness” and ranked them from 0 (smooth)-10 (rough). 20 panellists have been evaluated.
This procedure is standard in cosmetic industry and described in: Morten C. Meilgaard/Gail Vance Civille/B. Thomas Carr “Sensory Evaluation Techniques”; CRC Press, 4 th edition, Chapter 7: Attribute Difference Tests.
Result:
The statistical comparison of the mean values of the sample ranking shows that the two samples have a significantly different skin feel in terms of smoothness (based on a significance level of α=0.05).
The pigments of example 1 have a significantly better skin feel than the pigments of comparative example 2.
III. Applications
With both pearlescent pigments, i.e. according to example 1 and comparative example 2, a number of cosmetic applications were prepared and compared (see 11. Applications).
Example 9
Body Powder











Product
%


INCI Name
Name
W/W
Supplier










A

100.00


Mica
Silk Mica
40.70
www.vwr.com

Talc
Talc Powder
18.00
www.riedeldehaen.com

Boron Nitride
Softouch CCS 102
5.00
www.advceramics.com

Nylon 12
Orgasol 2002 D/Nat
8.00
www.atofinachemicals.com

Magnesium Stearate
Magnesium Stearate
6.00
www.sigmaaldrich.com

Methylparaben, Propylparaben
Rokonsal SSH-1
0.30
www.biochema.com

Mica (and) Iron Oxides
Prestige ® Soft Bronze
9.00
www.eckart.net

Pearlescent pigment
—
2.00


according to example 1




Mica (and) Titanium Dioxide
Prestige ® Magic Orange
9.00
www.eckart.net

B




Tridecyl Stearate (and) Tridecyl
Lipovol MOS-130
2.00
www.lipochemicals.com

Trimellitate (and) Dipentaerythrityl




Hexacaprylate/Hexacaprate



Procedure:

1. Mix the ingredients of phase A

2. Add phase B to Phase A

3. Mix well and fill into a vessel





































Comparative Example 10
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The body powder of example 9 showed a better gloss and a softer skin feel compared to the composition with ECR-Glass flakes.
Example 11
Cream Eye Shadow










INCI Name
Product Name
% W/W
Supplier










A

100.00


Castor Oil
Castor Oil
31.70
www.riedeldehaen.com

Octyl Palmitate
Liponate EHP
6.00
www.lipochemicals.com

Cocos Nucifera (Coconut) Oil
Lipovol C-76
7.00
www.lipochemicals.com

Bees Wax
Ewacera 12
6.00
www.wagnerlanolin.com

Isopropyl Lanolate
Ewalan IP
5.00
www.wagnerlanolin.com

Persea Gratissima (Avocado) Oil
Avocado Butter
7.00
www.impag.de

and Hydrogenated Avocado Oil




Magnesium Stearate
Magnesium Stearate
3.00
www.sigmaaldrich.com

Bis-Hydroxyethoxypropyl
Dow Corning 5562 Carbinol
7.00
www.dowcorning.com

Dimethicone
Fluid



Dimethicone/Vinyl Dimethicone
Dow Corning 9701 Cosmetic
5.00
www.dowcorning.com

Crosspolymer and Silica
Powder



Phenoxyethanol (and)
Uniphen P-23
0.30
www.induchem.com

Methylparaben (and)




Ethylparaben (and) Butylparaben




B




Mica (and) Iron Oxides
Prestige ® Soft Bronze
21.00
www.eckart.net

Pearlescent pigment according

1.00


to example 1



Procedure:

1. Mix phase A and heat up to 85° C.

2. Pre-mix phase B

3. Add phase B to phase A while stirring

4. Pour into an appropriate container

5. Cool down to RT











































Comparative Example 12
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The cream eye shadow of example 11 showed a better gloss and a softer skin feel compared to the composition with ECR-Glass flakes.
Example 13
Foundation










INCI Name
Product Name
% W/W
Supplier










A

100.00


Hydrogenated Polydecene
Ritadecene 20
9.00
www.ritacorp.com

Caprylic/Capric Triglyceride
Liponate GC-K
5.00
www.lipochemicals.com

Prunus Amygdalus Dulcis (Sweet
Sweet Almond Oil
4.00
www.jandekker.com

Almond) Oil

Caprylyl Trimethicone
SilCare Silicone 31M50
4.00
www.clariant.com

Caprylyl Methicone
SilCare Silicone 41M15
3.00
www.clariant.com

Steareth-2
Volpo S2
1.60
www.croda.com

Steareth-20
Sympatens AS/200 G
2.40
www.kolb.ch

B

Talc
Talc Powder
4.50
www.vwr.com

Mica (and) Iron Oxides
Prestige ® Soft Beige
4.00
www.eckart.net

Mica (and) Titanium Dioxide
Prestige ® Soft Silver
1.00
www.eckart.net

Pearlescent pigment according

0.50

to example 1

C

Glycerin
Pricerine 9090
5.00
www.brenntag.com

Water
Aqua
55.20

Ammonium
Aristoflex AVC
0.40
www.simon-und-werner.com

Acryloyldimehtyltaurate/VP

Copolymer

D

Propylene Glycol (and)
Nipaguard PDU
0.40
www.simon-und-werner.com

Diazolidinyl Urea (and)

Methylparaben (and)

Propylparaben



Procedure:

1. Heat phase A to 70° C. while stirring

2. Add the ingredients of phase B to phase A

3. Mix phase C well until Aristoflex is dissolved

4. Heat the mixture to 70° C.

5. Add phase C to phase AB

6. Cool down to 40° C. and add phase D


















































Comparative Example 14
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The foundation of example 13 showed a better gloss and a softer skin feel compared to the composition with ECR-Glass flakes.
Example 15
Lip Gloss










INCI Name
Product Name
% W/W
Supplier










A

100.00


Hydrogenated Polyisobutene
Versagel ME 750
79.00
www.penreco.com

(and) Ethylene/Propylene/Styrene

Copolymer (and)

Butylene/Ethylene/Styrene

Copolymer

Simmondsia Chinensis (Jojoba)
Jojoba Oil - Natural/Golden
2.00
www.biochemica.com

Seed Oil

Caprylyl Trimethicone
Silcare Silicone 31M50
7.00
www.clariant.com

Stearyl Dimethicone
Silcare Silicone 41M65
3.20
www.clariant.com

Hydrogenated Polydecene
Nexbase 2002
4.00
www.jandekker.com

Isopropyl Myristate
Isopropyl Myristate
4.50
www.vwr.com

B

Pearlescent pigment according

0.10

to example 1

Propylparaben
Propyl-4-hydroxybenzoat
0.20
www.sigmaaldrich.com



Procedure

1. Heat phase A to 85° C.

2. Add phase B to phase A and mix until uniform

3. Pour into a lip gloss vessel





































Comparative Example 16
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The lip gloss of example 15 showed a better gloss compared to the composition with ECR-Glass flakes.
Example 17
Lip Liner










INCI Name
Product Name
% W/W
Supplier










A

100.00


Hydrogenated Coco-Glycerides
Softisan 100
12.35
www.sasolwax.com

Candelilla Wax
Ewacera 42
14.00
www.wagnerlanolin.de

Magnesium Stearate
Magnesium Stearate
6.00
www.sigmaaldrich.com

Stearic Acid
Kortacid 1895
8.50
www.akzonobel.com

Hydrogenated Coconut Oil
Lipex 401
8.00
www.karlshamns.com

Cetyl Palmitate
Walrath synthetic
7.00
www.kahlwax.de

Caprylic/Capric Triglyceride
Liponate GC-K
3.60
www.lipochemicals.com

Soybean Glycerides (and)
Lipex L′sens
15.00
www.karlshamns.com


Butyrospermum Parkii


Tocopheryl Acetate
D,L-Alpha-Tocopherolacetat
0.25
www.dsm.com

Methylparaben; Propylparaben
Rokonsal SSH-1
0.30
www.biochema.com

B

Mica (and) Titanium Dioxide
Prestige ® Sapphire
7.50
www.eckart.net

(and) Ferric Ferrocyanide

Mica (and) Iron Oxides
Prestige ® Copper
7.50
www.eckart.net

Mica (and) Titanium Dioxide
Prestige ® Soft Silver
5.00
www.eckart.net

Pearlescent pigment according

5.00

to example 1



Procedure:

1. Heat phase A to 85° C.

2. Add phase B to phase A and mix until uniform

3. Poor into a Stick mold and cool








































Comparative Example 18
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The lip liner of example 17 showed a better gloss compared to the composition with ECR-Glass flakes.
Example 19
Lip-Stick










INCI Name
Product Name
% W/W
Supplier










A

100.00


Carnauba Wax
Ewacera 34
4.50
www.wagnerlanolin.de

Bees Wax
Ewacera 12
3.50
www.wagnerlanolin.de

Candelilla Wax
Ewacera 42
4.00
www.wagnerlanolin.de

Microcrystalline Wax
Parcera MW
7.20
www.paramelt.com

Cetyl Palmitate
Walrath synthetic
2.00
www.kahlwax.de

Hydrogenated Coco-Glycerides
Softisan 100
5.00
www.sasolwax.com

Petrolatum
Penreco Blond
5.80
www.penreco.com

Cetearyl Octanoate
Luvitol EHO
10.70
www.basf.com

Tocopheryl Acetate
D,L-Alpha-Tocopherolacetat
0.50
www.dsm.com

Castor Oil
Castor Oil
39.60
www.riedeldehaen.com

B

Mica (and) Iron Oxide
Prestige ® Fire-red
16.00
www.eckart.net

Pearlescent pigment according

1.00

to example 1

Methylparaben, Propylparaben
Rokonsal SSH-1
0.20
www.biochema.com



Procedure:

1. Heat phase A to 85° C.

2. Add phase B to phase A and mix until uniform

3. Poor into a lipstick mold at 75° C.





































Comparative Example 20
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The lip-stick of example 19 showed a better gloss and a better skin feeling compared to the composition with ECR-Glass flakes.
Example 21
Liquid Eyeliner










INCI Name
Product Name
% W/W
Supplier










A

100.00


Water
Aqua
68.70

Water/carbon black dispersion
MBD 201
3.00
www.geotech.nl

Acrylates Copolymer
Covacryl E14
10.00
www.lcw.fr

Magnesium Aluminium Silicate
Veegum HV
1.00
www.cherbsloeh.de

B

Propylene Glycol
1,2 Propandiol
3.00
www.vwr.com

Triethanolamine
Triethanolamine
1.40
www.vwr.com

C

Xanthan Gum
Keltrol T
0.30
www.cpkelco.com

D

Pearlescent pigment

1.00

according to example 1

Mica
Silk Mica
2.00
www.vwr.com

E

Stearic Acid
Kortacid 1895
2.80
www.akzonobel.de

Glyceryl Stearate
Aldo MS K FG
0.80
www.lonza.com

Oleyl Alcohol
HD-Ocenol 90/95 V
0.50
www.biesterfeld.com

Phenoxyethanol (and)
Uniphen P-23
0.50
www.induchem.com

Methylparaben (and)

Ethylparaben (and)

Butylparaben

F

Dimethicone (and) Trisiloxane
Dow Corning 2-1184 Fluid
5.00
www.dowchemicals.com



Procedure:

1. Disperse Veegum in phase A

2. Stirr for 15 minutes

3. Add phase B to phase A

4. Add phase C to phase AB

5. Stirr for 10 minutes

6. Add phase D to phase ABC and heat to 75° C.

7. Heat phase E to 75° C.

8. Add phase E to phase ABCD

9. Cool down to 60° C. and add phase F



















































Comparative Example 22
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The eyeliner of example 21 showed a better gloss and a better skin feeling compared to the composition with ECR-Glass flakes.
Example 23
Mascara










INCI Name
Product Name
% W/W
Supplier










A

100.00


Water
Aqua
66.00

Propylene Glycol
1,2 Propanediol
1.50
www.vwr.com

Pearlescent pigment according

1.30

to example 1

Cosmetic Black Oxide
C 33-134 Cosmetic Black
7.00
www.sunchemical.com


Oxide

Caprylic/Capric Triglyceride
Liponate GC-K
2.00
www.lipochemicals.com

Hydroxyethylcellulose
Cellosize HEC QP-52000H
0.30
www.dow.com

Magnesium Alumium Silicate
Veegum HV
1.80
www.rtvanderbilt.com

B

Carnauba Wax
Ewacera 34
3.00
www.wagnerlanolin.de

Bees Wax
Ewacera 12
3.00
www.wagnerlanolin.de

Glyceryl Stearate
Imwitor 960 K
3.00
www.sasolwax.xom

Cetyl Alcohol
Cetyl Alcohol
3.80
www.vwr.com

Polysorbate 60
Tween 60 V
1.00
www.uniqema.com

PVP/VA Copolymer
Luviskol VA 64
2.00
www.basf.com

C

Water
Aqua
4.00

BHT
Tenox BHT Kosher
0.10
www.eastman.com

Methylparaben
Methyl-4-hydroxybenzoate
0.20
www.sigmaaldrich.com



Procedure:

1. Heat phase A to 85° C. with stirring

2. Heat phase B to 85° C.

3. Mix phase B into phase A

4. Cool down to 55° C. while stirring

5. Add phase C and mix well

6. Fill into Mascara Set













































Comparative Example 24
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The mascara of example 23 showed a better gloss and a better skin feeling compared to the composition with ECR-Glass flakes.
Example 25
Mousse










INCI Name
Product Name
% W/W
Designated use










A

100.00


Cyclopentasiloxane
Dow Corning 245 Fluid
8.60
www.dowcorning.com

Hydrogenated Polyisobutene
MC 30
4.00
www.sophim.com

Dimethicone (and) Dimethicone
Dow Corning 9041 Silicone
34.14
www.dowcorning.com

Crosspolymer
Elastomer Blend

Squalane
Squalane
5.74
www.impag.de

Isononyl Isononanoate
Dermol 99
10.16
www.alzointernational.com

Hydrogenated Jojoba Oil
Jojoba Butter LM
2.15
www.desertwhale.com

Hydrogenated Jojaba Oil
Jojoba Butter HM
1.00
www.desertwhale.com

C30-45 Alkyl Methicone (and)
Dow Corning AMS-C30
1.15
www.dowcorning.com

C30-45 Olefin
Cosmetic Wax

Stearyl Dimethicone
Dow Corning 2503 Cosmetic
0.47
www.dowcorning.com


Wax

Cyclopentasiloxane (and)
Dow Corning 670 Fluid
5.00
www.dowcorning.com

Polypropylsilsesquioxane

B

Dimethicone/Vinyl Dimethicone
Dow Corning 9506 Powder
16.02
www.dowcorning.com

Crosspolymer

Silica Dimethyl Silylate
Covasilic 15
0.17
www.lcw.fr

Talc
Talc Powder
5.00
www.riedeldehaen.com

Mica (and) Titanium Dioxide
Prestige ® Soft Beige
5.00
www.eckart.net

(and) Iron Oxides

Pearlescent pigment according

1.00

to example 1

C

Propylene Glycol, Diazolidinyl
Germaben II
0.40
www.ispcorp.com

Urea, Methylparaben,

Propylparaben



Procodure:

1. Mix ingredients of phase A and heat until melted

2. Pre-mix phase B with speed mixer (2400 rpm, 1 min)

3. Add half part of molten phase A to phase B and mix with speed mixer (2400 rpm, 30 s)

4. Add reminder of phase A to phase B and mix with speed mixer (2400 rpm, 30 s)

5. Add phase C and mix with speed mixer (2400 rpm, 30 s)

6. Cool down to room temperature




















































Comparative Example 26
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The mousse of example 25 showed a better gloss and a better skin feeling compared to the composition with ECR-Glass flakes.
Example 27
Nail Polish










INCI Name
Product Name
% W/W
Supplier










A

100.00


Pearlescent

2.00
www.eckart.net

pigment

according

to

example 1

B

International
Butylacetat (and)
98.00
www.internationallacquers.lu

Lacquers
Ethylacetat (and)

Nailpolish
Nitrocellulose

& Care
(and)

Base 359
Isopropyl Alcohol



Procedure:

1. Mix phase A with B with stirring

2. Pour into an appropriate container
































Comparative Example 28
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The nail polish of example 27 showed a better gloss compared to the composition with ECR-Glass flakes.
Example 29
Pressed Eye Shadow










INCI Name
Product Name
% W/W
Supplier










A

100.00


Mica
Silk Mica
17.00
www.vwr.com

Boron Nitride
Softouch CCS 102
2.50
www.advceramicscos.com

Talc
Talc Powder
23.50
www.riedeldehaen.com

Zinc Stearate
Kemilub EZ-V
7.00
www.undesa.com

Mica (and) Iron Oxides
Prestige ® Bright Fire-red
39.00
www.eckart.net

Pearlescent pigment according

1.00

to example 1

B

Dimethicone
Dow Corning ® 200 Fluid 5 cst
5.00
www.dowcorning.com

Cyclomethicone (and)
Dow Corning ® 9040 Elastomer
5.00
www.dowcorning.com

Dimethicone Crosspolymer



Procedure:

1. Mix phase A

2. Add phase B and stir until homogeneous

3. Press eye shadow at 150 bar for 30 min

































Comparative Example 30
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The eye shadow of example 29 showed a better gloss compared to the composition with ECR-Glass flakes.
Example 31
Pressed Powder










INCI Name
Product Name
% W/W
Supplier










A

100.00


Talc
Talc Powder
51.70
www.riedeldehaen.com

Zinc Stearate
Kemilub EZ-V
5.00
www.undesa.com

Methylparaben, Propylparaben
Rokonsal SSH-1
0.30
www.biochema.com

Polyethylene
Asensa CL 111
20.50
www.honeywell.com

Silica
Syloblanc 34
1.50
www.gracedavision.com

Mica (and) Titanium Dioxide
Prestige ® Soft Silver
6.00
www.eckart.net

Mica (and) Titanium Dioxide
Prestige ® Soft Beige
11.00
www.eckart.net

(and) Iron Oxides

Pearlescent pigment according

1.00

to example 1

B

Octyl Palmitate
Liponate EHP
3.00
www.lipochemicals.com



Procedure:

1. Mix phase A

2. Add phase B and stir until homogeneous

3. Press eye shadow at 150 bar for 30 min


































Comparative Example 32
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The pressed powder of example 31 showed a better gloss compared to the composition with ECR-Glass flakes.
Example 33
Shower Gel










INCI Name
Product Name
% W/W
Supplier










A

100.00


Pearlescent pigment according

0.01

to example 1

Water
Aqua
67.94

Blue 1 (0.5% aqueous solution)
FD&C Blue No. 1
0.10
www.sunchemicals.com

Acrylates/C10-30 Alkyl Acrylate
Carbopol ETD 2020
1.00
www.noveon.com

Crosspolymer

Propylene Glycol
1,2-Propanediol
1.00
www.vwr.com

B

TEA-Lauryl Sulfate
Texapon T 42
22.00
www.cognis.com

Cocamide Dea
Rewomid DC 212 S
3.00
www.degussa.com

Cocamidopropyl Betaine
Tego Betain F 50
4.00
www.cognis.com

Disodium EDTA
Edeta BD
0.05
www.basf.com

C

Triethanolamine
Triethanolamine
0.30
www.vwr.com

Phenoxyethanol,
Euxyl PE 9010
0.60
www.schuelke-mayr.com

Ethylhexylglycerin



Procedure:

1. Disperse Carbopol in phase A

2. Heat phase to 65° C.

3. Add one by one the ingredients of phase B

4. Cool down and continue to stir. When 40-45° C. are reached add phase C







































Comparative Example 34
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The shower gel of example 33 showed a better gloss compared to the composition with ECR-Glass flakes.
Example 35
Styling Soft Wax










INCI Name
Product Name
% W/W
Supplier










A

100.00


Pearlescent pigment according

0.10

to example 1

Water
Aqua
53.40

Propylene Glycol
1,2 Propanediol
2.00
www.vwr.com

Glycerin
Pricerine 9090
7.00
www.uniqema.com

Methoxy PEG/PPG-7/3
Abil Soft AF 100
0.50
www.degussa.com

Aminopropyl Dimethicone

B

Isosteareth-20
Procol IS-20
14.50
www.protameen.com

Laureth-4
Genapol LA 040
10.00
www.clariant.com

Paraffinum Liquidium
Paraffinum Liquidium
6.00
www.heess.de

C12-15 Alkyl Benzoate
Sympatens-LBZ
6.00
www.kolb.ch

C

Phenoxyethanol (and)
Phenonip
0.40
www.clariant.com

Methylparaben (and)

Butylparaben (and) Ethylparaben

(and) Propylparaben (and)

Isobutylparaben

Fragrance
Cool Floral OA D
0.10
www.bell-europe.com



Procedure:

1. Heat phase A and B seperatly to 90° C.

2. Add phase B to phase A while stirring

3. Cool down to 55° C.

4. Add phase C and fill into jar










































Comparative Example 36
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The Styling Soft Wax of example 35 showed a better gloss compared to the composition with ECR-Glass flakes.
Example 37
Sun Protection Cream










INCI Name
Product Name
% W/W
Supplier










A

100.00


Sorbitan Stearate (and) Methyl
Sympatens-O/2500 G
5.00
www.kolb.ch

Glucose Sesquistearte

Stearic Acid
Kortacid 1895
4.00
www.akzonobel.com

Octyldodecanol
Eutanol G
9.00
www.cognis.com

Caprylic/Capric Triglyceride
Liponate GC-K
10.00
www.lipochemicals.com

Cetearyl Alcohol
Lanette O
2.00
www.cognis.com

Macadamia ternifolia Seed Oil
Macadamia Nut Oil
3.20
www.jandekker.com

Octyl Methoxycinnamate
Parsol MCX
1.00
www.dsm.com

Butyl Methoxydibenzoylmethane
Parsol 1789
5.00
www.roche.com

B

Pearlescent pigment according

0.70

to example 1

Water
Aqua
56.35

Glycerin
Pricerine 9090
3.20
www.uniqema.com

C

Phenoxyethanol (and)
Uniphen P-23
0.40
www.induchem.com

Methylparaben (and)

Ethylparaben (and) Butylparaben

Fragrance
Nivamar BM
0.15
www.bell-europe.com



Procedure:

1. Heat phase A and B seperately to 80° C.

2. Add phase A to phase B while stirring

3. Cool down to 45° C.

4. Add phase C










































Comparative Example 38
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The sun protection cream of example 37 showed a better gloss compared to the composition with ECR-Glass flakes.
Example 39
Transparent Lipstick










INCI Name
Product Name
% W/W
Supplier










A

100.00


Ethylenediamine/Hydrogenated
Sylvaclear A2614V
28.00
www.arizonachemical.com

Dimer Dilinoleate Copolymer Bis-

Di-C14-18 Alkyl Amide

Bis-Stearyl Ethylenediamine/
Sylvaclear C75V
28.00
www.arizonachemical.com

Neopentyl Glycol/Hydrogenated

Dimer Dilinoleate

Paraffinum Liquidum
Paraffinum Liquidum
13.80
www.heess.de

Macadamia Integrifolia Seed Oil
Floramac Hawaiian
10.00
www.floratech.com


Macadamia Oil-Refined

Isopropyl Myristate
Isopropyl Myristate
6.00
www.vwr.com

C12-15 Alkyl Benzoate
Sympatens-LBZ
6.00
www.kolb.ch

Caprylic/Capric Triglyceride
Miglyol 812
7.00
www.sasolwax.com

Propylparaben
Propyl-4-hydroxybenzoat
0.20
www.sigmaaldrich.com

B

Pearlescent pigment according

1.00
t

to example 1



Procedure:

1. Heat phase A to 85° C.

2. Add phase B to phase A and mix

3. Poor into lipstick mould at 75° C.






































Comparative Example 40
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The Transparent lip-stick of example 39 showed a better gloss compared to the composition with ECR-Glass flakes.
Example 41
Body Lotion Water-In-Silicone










INCI Name
Product Name
% W/W
Supplier










A

100.00


Cyclopentasiloxane (and)
Dow Corning 1501
11.50
www.dowcorning.com

Dimethiconol

Cyclopentasiloxane
Dow Corning 245
5.75
www.dowcorning.com

Cyclopentasiloxane (and)
Dow Corning 5225 C
13.80
www.dowcorning.com

PEG/PPG/— 18/18 Dimethicone

C 30-45 Alkyl Methicone
Dow Corning Cosmetic Wax
3.45
www.dowcorning.com


AMS-C30

Pearlescent pigment according

0.70

to example 1

C

Polysorbate 20
Tween 20
0.60
www.uniqema.com

Phenoxyethanol (and)
Uniphen P-23
0.35
www.induchem.com

Methylparaben (and)

Ethylparaben (and) Butylparaben

Sodium Chloride
Sodium Chloride
0.75
www.vwr.com

Water
Aqua
63.10



Procedure:

1. Mix phase A and heat up to 75° C.

2. Mix phase B and heat up to 70° C.

3. Add phase B slowly to phase A under homogenisation

4. Cool down while stirring







































Comparative Example 42
Same Composition as Above Using Pearlescent Pigments of Comparative Example 2
The Body Lotion of example 41 showed a better gloss compared to the composition with ECR-Glass flakes.