Cosmetic preparation for priming prior to the application of make-up

WO2026166880A1PCT designated stage Publication Date: 2026-08-13BEIERSDORF AG
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Authority / Receiving Office
WO · WO
Patent Type
Applications
Current Assignee / Owner
Filing Date
2026-01-30
Publication Date
2026-08-13

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Abstract

Cosmetic O / W emulsion containing a) one or more UV filters, b) an emulsifier system, c) di(propylene glycol) dibenzoate (INCI: Dipropylene Glycol Dibenzoate), wherein the preparation is free of polyacrylates, cross-linked acrylate / C10-C30 alkyl acrylate polymers, vinylpyrrolidone / hexadecene copolymers, 3-(4-methylbenzylidene)camphor, 2-hydroxy-4-methoxybenzophenone (INCI: Oxybenzone), 4-methoxycinnamate-2-ethylhexyl ester (INCI: Octyl Methoxycinnamate), ethylhexyl 2-cyano-3,3-diphenylacrylate (INCI: Octocrylene), parabens (in particular methyl-, propyl- and butylparaben), methylisothiazolinone, chloromethylisothiazolinone, DMDM hydantoin, mineral oils, mineral waxes and silicone oils.
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Description

[0001] Beiersdorf Aktiengesellschaft

[0002] Hamburg

[0003] Description

[0004] Cosmetic preparation for priming before applying make-up.

[0005] The present invention relates to a cosmetic O / W emulsion containing one or more UV filters, an emulsifier system, one or more oils selected from the group consisting of di(propylene glycol) dibenzoate (INCI: Dipropylene Glycol Dibenzoate), benzyl benzoate (INCI: Benzyl Benzoate) and C12-15 alkyl benzoate (INCI: C12-15 Alkyl Benzoate), wherein the preparation is free of polyacrylates, cross-linked acrylate / C10-C30 alkyl acrylate polymers, vinylpyrrolidone / hexadecene copolymers, 3-(4-methylbenzylidene) camphor, 2-hydroxy-4-methoxybenzophenone (INCI: Oxybenzone), 4-methoxycinnamate-2-ethylhexyl ester (INCI: Octylmethoxycinnamate), and ethylhexyl-2-cyano-3,3-diphenyl acrylate (INCI: Octocrylene). Parabens (especially methyl, propyl and butylparaben), methylisothiazolinone, chloromethylisothiazolinone, DMDM ​​hydantoin, mineral oils, mineral waxes and silicone oils, and their use.

[0006] The desire to look beautiful and attractive is rooted in human nature. Even though the ideal of beauty has changed over time, the pursuit of a flawless appearance has always been a human goal. The condition and appearance of the skin plays a significant role in achieving a beautiful and attractive appearance.

[0007] For the skin to fully perform its biological functions, it requires regular cleansing and care. Cleansing the skin removes dirt, sweat, and dead skin cells, which provide an ideal breeding ground for pathogens and parasites of all kinds. Skin care products primarily moisturize and replenish the skin's natural oils. They often contain active ingredients that regenerate the skin or protect it from the harmful effects of UV radiation. A third group consists of decorative cosmetics—that is, makeup products—which influence the appearance of the skin and enhance its visual appeal (e.g., lipsticks, mascara, foundations).

[0008] Difficulties in the application of cosmetics arise particularly when different products from these categories are to be combined.

[0009] Applying makeup to skin areas treated with skincare products presents a particular challenge. This is especially problematic when applying makeup to areas pre-treated with sunscreen, as the makeup does not adhere well to the sunscreen.

[0010] However, even on "untreated" skin, with its unevenness and color variations (for example, from age spots), makeup products often don't adhere evenly. For this reason, so-called "primer" preparations have been offered for several years. These form a kind of base on the skin, even out the complexion, and allow the subsequently applied makeup to truly shine. These "primer" preparations typically contain larger quantities of silicone oils, which enhances their cosmetic effect, but are increasingly viewed critically for environmental and resource conservation reasons. While silicone oils generally prevent the "white cast" of the product on the skin, they are not naturally occurring raw materials but must be synthetically produced. Consequently, they degrade slowly in the environment. For this reason, there is a growing interest in formulating cosmetic preparations without silicone oils.The object of the present invention was therefore to develop a silicone oil-free primer preparation that does not leave a white residue. "White residue" is understood by those skilled in the art to mean the formation of white streaks and residues on the skin during and after the application of a cosmetic preparation.

[0011] Furthermore, incorporating UV filters into primer formulations has proven difficult in the past. When using UV filters, it is desirable for a stable film (containing the UV filters) to remain on the skin. Primers, on the other hand, are intended to be absorbed quickly and completely into the skin. Since most UV filters are also organic compounds, their compatibility with the lipid phase of makeup products is often compromised. As a rule, the use of organic UV filters results in the makeup no longer adhering properly to the skin or flaking off relatively quickly.

[0012] The object of the present invention was therefore to develop a primrose preparation containing UV filters, on which make-up products can be applied well and evenly and adhere significantly more stably than on conventional primer products.

[0013] The tasks are surprisingly solved by a cosmetic O / W emulsion containing a) one or more UV filters,

[0014] b) an emulsifier system,

[0015] c) Di(propylene glycol) dibenzoate (INCI: Dipropylene Glycol Dibenzoate),

[0016] the preparation is free of polyacrylates, cross-linked acrylate / C 10-030 alkyl acrylate polymers, vinylpyrrolidone / hexadecene copolymers, 3-(4-methylbenzylidene) camphor, 2-hydroxy-4-methoxybenzophenone (INCI: oxybenzone), 4-methoxycinnamate-2-ethylhexyl ester (INCI: octyl methoxycinnamate), ethylhexyl-2-cyano-3,3-diphenyl acrylate (INCI: octocrylene), parabens (especially methyl, propyl, and butylparaben), methylisothiazolinone, chloromethylisothiazolinone, DMDM ​​hydantoin, mineral oils, mineral waxes, and silicone oils. The tasks are also surprisingly accomplished by using a cosmetic O / W emulsion containing

[0017] a) one or more UV filters,

[0018] b) an emulsifier system,

[0019] c) one or more oils selected from the group Di(propylene glycol) dibenzoate (INCI:

[0020] Dipropylene glycol dibenzoate), benzyl benzoate (INCI: Benzyl Benzoate) and C12-15 alkyl benzoate (INCI: C12-15 Alkyl Benzoate), wherein the preparation is free from polyacrylates, cross-linked acrylate / C10-C30 alkyl acrylate polymers, vinylpyrrolidone / hexadecene copolymers, 3-(4-methylbenzylidene) camphor, 2-hydroxy-4-methoxybenzophenone (INCI: Oxybenzone), 4-methoxycinnamate-2-ethylhexyl ester (INCI: Octyl methoxycinnamate), ethylhexyl 2-cyano-3,3-diphenyl acrylate (INCI: Octocrylene), parabens (especially methyl, propyl, and butyl parabens), methylisothiazolinone, chloromethylisothiazolinone, DMDM ​​hydantoin, mineral oils, mineral waxes, and Silicone oils, for cosmetic treatment of the skin before applying make-up (primer).

[0021] According to the invention, the use of one or more oils selected from the group consisting of di(propylene glycol) dibenzoate (INCI: Dipropylene Glycol Dibenzoate), benzyl benzoate (INCI: Benzyl Benzoate), and C12-15 alkyl benzoate (INCI: C12-15 Alkyl Benzoate) in a cosmetic O / W emulsion for the cosmetic treatment of the skin before the application of make-up (primer), to improve the adhesion of make-up to the skin is also included.

[0022] According to the invention, one of the methods is for applying make-up to the skin, wherein in a first step a cosmetic O / W emulsion is used.

[0023] a) one or more UV filters,

[0024] b) an emulsifier system,

[0025] c) one or more oils selected from the group Di(propylene glycol) dibenzoate (INCI:

[0026] Dipropylene glycol dibenzoate), benzyl benzoate (INCI: Benzyl Benzoate), and C12-15 alkyl benzoate (INCI: C12-15 Alkyl Benzoate), wherein the preparation is free from polyacrylates, cross-linked acrylate / C10-C30 alkyl acrylate polymers, vinylpyrrolidone / hexadecene copolymers, 3-(4-methylbenzylidene) camphor, 2-hydroxy-4-methoxybenzophenone (INCI: Oxybenzone), 4-methoxycinnamate-2-ethylhexyl ester (INCI: Octyl methoxycinnamate), ethylhexyl 2-cyano-3,3-diphenyl acrylate (INCI: Octocrylene), parabens (especially methyl, propyl, and butyl parabens), methylisothiazolinone, chloromethylisothiazolinone, DMDM ​​hydantoin, mineral oils, mineral waxes, and silicone oils are applied to the skin, and then in a second step the make-up is applied to the pre-treated skin.

[0027] For the use and the method according to the invention, it is preferred if the oils c) are a combination of di(propylene glycol) dibenzoate (INCI: Dipropylene Glycol Dibenzoate) and benzyl benzoate (INCI: Benzyl Benzoate) or di(propylene glycol) dibenzoate (INCI: Dipropylene Glycol Dibenzoate).

[0028] Within the scope of the present disclosure, the terms “according to the invention”, “preparation according to the invention”, etc., always refer to the preparations, processes and uses according to the invention, i.e. also to preparations in which the uses according to the invention are realized, as well as preparations with which the process according to the invention is realized.

[0029] It is advantageous within the meaning of the present invention if the oils c) are used in a total amount of 1 to 9% by weight, based on the total weight of the preparation. According to the invention, it is preferred if di(propylene glycol) dibenzoate (INCI: Dipropylene Glycol Dibenzoate) is used in a total amount of 1 to 4% by weight, based on the total weight of the preparation.

[0030] For benzyl benzoate (INCI: Benzyl Benzoate) the advantageous concentration according to the invention is 0.001-0.5 wt%, based on the total weight of the preparation.

[0031] According to the invention, it is advantageous if a combination of hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate (INCI: Diethylamino hydroxybenzoyl hexyl benzoate), 2,4,6-tris-[anilino-(p-carbo-2'-ethyl-T-hexyloxy)]-1,3,5-triazine (INCI: Ethylhexyl Triazone), 2,4-bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis- Ethylhexyloxyphenol methoxyphenyl Triazine), 4-(tert-Butyl)-4'-methoxydibenzoylmethane and 2-phenylbenzimidazole-5-sulfonic acid salts is used as a UV filter.

[0032] According to the invention, it is preferred if hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate (INCI: Diethylamino hydroxybenzoyl hexyl benzoate) is used in a concentration of more than 0.5 wt%, based on the total weight of the preparation.

[0033] According to the invention, it is preferred if 2,4,6-Tris-[anilino-(p-carbo-2'-ethyl-1'-hexyloxy)]-1,3,5-triazine (INCI: Ethylhexyl Triazone) is used in a concentration of 0.5 to 4 wt%, based on the total weight of the preparation.

[0034] According to the invention, it is preferred if 2,4-Bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis- Ethylhexyloxyphenol methoxyphenyl Triazine) is used in a concentration of 0.5 to 6 wt% based on the total weight of the preparation.

[0035] According to the invention, it is preferred if 4-(tert-Butyl)-4'-methoxydibenzoylmethane is used in a concentration of 0.5 to 6 wt% based on the total weight of the preparation.

[0036] According to the invention, it is preferred if 2-phenylbenzimidazole-5-sulfonic acid salts are used in a concentration of 0.5 to 4% by weight, based on the total weight of the preparation. Furthermore, the sodium salt is preferably used according to the invention.

[0037] Advantageous embodiments of the present invention are further characterized in that the preparation is free of ethylhexyl salicylate and homomenthyl salicylate (INCI: Homosalate).

[0038] Furthermore, it is advantageous in the sense of the present invention if the preparation as an emulsifier system b) contains a mixture of sodium cetearyl sulfate (INCI: Sodium Cetearyl Sulfate), self-emulsifying glyceryl stearate (INCI: Glyceryl Stearate SE) and polyglyceryl-3 methylglucose distearate (INCI: Polyglyceryl-3 Methylglucose Distearate).

[0039] The advantageous concentrations according to the invention are, for sodium cetearyl sulfate (INCI: Sodium Cetearyl Sulfate), 0.05 to 2% by weight, based on the total weight of the preparation, for

[0040] Self-emulsifying glyceryl stearate (INCI: Glyceryl Stearate SE) of 0.5 to 4% by weight, based on the total weight of the preparation and for

[0041] Polyglyceryl-3 methylglucose distearate (INCI: Polyglyceryl-3 Methylglucose Distearate) from 0.05 to 2% by weight, based on the total weight of the preparation.

[0042] Furthermore, advantageous embodiments of the present invention are characterized in that the preparation is free of EDTA and its sodium salts.

[0043] Instead, according to the invention, it is advantageous if the preparation contains sodium salts of ethylenediamine disuccinate (INCI: Ethylenediamine Disuccinate, EDDS), wherein the sodium salt is preferably used according to the invention.

[0044] According to the invention, it is advantageous if the preparation contains C12-15 alkyl benzoate (INCI: C12-15 Alkyl Benzoate). In such a case, C12-15 alkyl benzoate is preferably used in a concentration of 0.5 to 6% by weight, based on the total weight of the preparation. Furthermore, advantageous embodiments according to the invention are characterized in that the preparation contains a combination of microcrystalline cellulose (INCI: Microcrystalline Cellulose) and carboxymethyl cellulose (INCI: Cellulose Gum).

[0045] Furthermore, according to the invention, it is advantageous if the preparation contains a combination of distarch phosphate (INCI: Distarch Phosphate), tapioca starch (INCI: Tapioca Starch) and silica dimethyl silylate (INCI: Silica Dimethyl Silylate).

[0046] It is also advantageous in the sense of the present invention if the preparation contains Diisostearoylpolyglyceryl-3-dimerdilinoleate (INCI: Diisostearoyl Polyglyceryl-3 Dilinoleate).

[0047] Advantageous embodiments of the present invention are characterized, not least, by the fact that the preparation contains one or more lipids from the group of compounds dibutyl adipate, cetyl palmitate, isopropyl palmitate, carnauba wax and hydrogenated rapeseed oil.

[0048] comparative test

[0049] The inventive effect was demonstrated using the following comparative experiment: The following formulations were prepared and the adhesion of various make-up products was examined.

[0050]

[0051] The products were then applied in a quantity of 125pL to an area of ​​42.5 cm². 2 Applied to the inside of the forearm of 6 test subjects and allowed to absorb for a period of 2-3 minutes.

[0052] The essence "pure nude powder" makeup product was then applied to the treated area. After a waiting period of 4 hours at room temperature, and after a 2.5-minute application of a facial sauna, the application area was visually inspected and evaluated.

[0053] Result:

[0054] While in preparations 1 and 2 the make-up product was practically unrecognizable, in preparation 3 the make-up product could be recognized almost unchanged.

Claims

Patent claims 1. Cosmetic O / W emulsion containing a) one or more UV filters, b) an emulsifier system, c) Di(propylene glycol) dibenzoate (INCI: Dipropylene Glycol Dibenzoate), the preparation is free from polyacrylates, cross-linked acrylate / C 10-030 alkyl acrylate polymers, vinylpyrrolidone / hexadecene copolymers, 3-(4-methylbenzylidene) camphor, 2-hydroxy-4-methoxybenzophenone (INCI: oxybenzone), 4-methoxycinnamate-2-ethylhexyl ester (INCI: octyl methoxycinnamate), ethylhexyl-2-cyano-3,3-diphenyl acrylate (INCI: octocrylene), parabens (especially methyl, propyl and butyl parabens), methylisothiazolinone, chloromethylisothiazolinone, DMDM ​​hydantoin, mineral oils, mineral waxes and silicone oils.

2. Use of a cosmetic O / W emulsion containing a) one or more UV filters, b) an emulsifier system, c) one or more oils selected from the group consisting of di(propylene glycol) dibenzoate (INCI: Dipropylene Glycol Dibenzoate), benzyl benzoate (INCI: Benzyl Benzoate), and C12-15 alkyl benzoate (INCI: C12-15 Alkyl Benzoate), wherein the preparation is free from polyacrylates, cross-linked acrylate / C10-C30 alkyl acrylate polymers, vinylpyrrolidone / hexadecene copolymers, 3-(4-methylbenzylidene) camphor, 2-hydroxy-4-methoxybenzophenone (INCI: Oxybenzone), 4-methoxycinnamate-2-ethylhexyl ester (INCI: Octylmethoxycinnamate), ethylhexyl-2-cyano-3,3-diphenyl acrylate (INCI: Octocrylene), parabens (especially methyl, propyl and butylparaben), methylisothiazolinone, chloromethylisothiazolinone, DMDM ​​hydantoin, mineral oils, mineral waxes and silicone oils, for cosmetic treatment of the skin before applying make-up (primer).

3. Use of one or more oils selected from the group of di(propylene glycol) dibenzoate (INCI: Dipropylene Glycol Dibenzoate), benzyl benzoate (INCI: Benzyl Benzoate), and C12-15 alkyl benzoate (INCI: C12-15 Alkyl Benzoate) in a cosmetic O / W emulsion for cosmetic treatment of the skin prior to the application of make-up (primer), to improve the adhesion of make-up to the skin.

4. Method for applying make-up to the skin, wherein in a first step a cosmetic O / W emulsion containing a) one or more UV filters, b) an emulsifier system, c) one or more oils selected from the group consisting of di(propylene glycol) dibenzoate (INCI: Dipropylene Glycol Dibenzoate), benzyl benzoate (INCI: Benzyl Benzoate), and C12-15 alkyl benzoate (INCI: C12-15 Alkyl Benzoate), wherein the preparation is free from polyacrylates, cross-linked acrylate / C10-C30 alkyl acrylate polymers, vinylpyrrolidone / hexadecene copolymers, 3-(4-methylbenzylidene) camphor, 2-hydroxy-4-methoxybenzophenone (INCI: Oxybenzone), 4-methoxycinnamate-2-ethylhexyl ester (INCI: Octylmethoxycinnamate), ethylhexyl-2-cyano-3,3-diphenyl acrylate (INCI: Octocrylene), parabens (especially methyl, propyl and butylparaben), methylisothiazolinone, chloromethylisothiazolinone, DMDM ​​hydantoin, mineral oils, mineral waxes and silicone oils, is applied to the skin, and then in a second step the make-up is applied to the pre-treated skin.

5. Use or method according to one of the preceding claims, characterized in that c) Di(propylene glycol) dibenzoate (INCI: Dipropylene Glycol Dibenzoate) is used as the oil.

6. O / W emulsion, use or method according to any of the preceding claims, characterized in that the oils c) are used in a total quantity of 1 to 9% by weight, based on the total weight of the preparation.

7. O / W emulsion, use or method according to any of the preceding claims, characterized in that a) a combination of hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate (INCI: Diethylamino hydroxybenzoyl hexyl benzoate), 2,4,6-tris-[anilino-(p-carbo-2'-ethyl-T-hexyloxy)]-1,3,5-triazine (INCI: Ethylhexyl Triazone), 2,4-bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis-Ethylhexyloxyphenol methoxyphenyl Triazine), 4-(tert-Butyl)-4'-methoxydibenzoylmethane and 2-phenylbenzimidazole-5-sulfonic acid salts is used as a UV filter.

8. O / W emulsion, use or method according to any of the preceding claims, characterized in that the preparation is free of ethylhexyl salicylate and homomenthyl salicylate.

9. O / W emulsion, use or method according to any of the preceding claims, characterized in that the preparation as an emulsifier system b) contains a mixture of sodium cetearyl sulfate (INCI: Sodium Cetearyl Sulfate), self-emulsifying glyceryl stearate (INCI: Glyceryl Stearate SE) and polyglyceryl-3 methylglucose distearate (INCI: Polyglyceryl-3 Methylglucose Distearate).

10. O / W emulsion, use or method according to any of the preceding claims, characterized in that the preparation is free of EDTA and its sodium salts.

11. An oil-in-water (O / W) emulsion, use or method according to any one of the preceding claims, characterized in that the preparation contains sodium salts of ethylenediamine disuccinate (INCI: Ethylenediamine Disuccinate, EDDS).

12. An oil-in-water (O / W) emulsion, use or method according to any one of the preceding claims, characterized in that the preparation contains C12-15 alkyl benzoate (INCI: C12-15 Alkyl Benzoate).

13. O / W emulsion, use or method according to any of the preceding claims, characterized in that the preparation contains a combination of microcrystalline cellulose (INCI: Microcrystalline Cellulose) and carboxymethyl cellulose (INCI: Cellulose Gum).

14. O / W emulsion, use or method according to any of the preceding claims, characterized in that the preparation contains a combination of distarch phosphate (INCI: Distarch Phosphate), tapioca starch (INCI: Tapioca Starch) and silica dimethyl silylate (INCI: Silica Dimethyl Silylate).

15. O / W emulsion, use or method according to any of the preceding claims, characterized in that the preparation contains Diisostearoylpolyglyceryl-3- dimerdilinoleate (INCI: Diisostearoyl Polyglyceryl-3 Dilinoleate).

16. O / W emulsion, use or method according to any of the preceding claims, characterized in that the preparation contains one or more lipids from the group consisting of dibutyl adipate, cetyl palmitate, isopropyl palmitate, carnauba wax and hydrogenated rapeseed oil.