Cosmetic preparation with vanillin and ethylhexyloxyphenol methoxyphenyl triazine
A cosmetic preparation with 4-hydroxy-3-methoxybenzaldehyde, 2,4-bis{[4-(2-ethylhexyloxy)-2-hydroxy]phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine, and dibutyl adipate or butylene glycol dicaprylate/dicaprate addresses crystallization issues, preserving sensory and UV protection properties.
Patent Information
- Application Number
- DE102024203784
- Authority / Receiving Office
- DE · DE
- Patent Type
- Applications
- Current Assignee / Owner
- Filing Date
- 2024-04-23
- Publication Date
- 2025-10-23
AI Technical Summary
Cosmetic preparations containing 4-hydroxy-3-methoxybenzaldehyde (vanillin) and 2,4-bis{[4-(2-ethylhexyloxy)-2-hydroxy]phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (bis-ethylhexyloxyphenol methoxyphenyl triazine) suffer from crystallization issues under UV light, leading to reduced sensory properties and UV protection due to the precipitation of these compounds.
A cosmetic preparation comprising 4-hydroxy-3-methoxybenzaldehyde, 2,4-bis{[4-(2-ethylhexyloxy)-2-hydroxy]phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine, and dibutyl adipate and/or butylene glycol dicaprylate/dicaprate is used to prevent crystallization, maintaining sensory properties and UV protection.
The combination effectively prevents crystallization and maintains UV protection, ensuring stable sensory qualities over extended periods.
Abstract
Description
[0001] The present invention relates to a cosmetic preparation containing 4-hydroxy-3-methoxybenzaldehyde (INCI: Vanillin), 2,4-bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis-Ethylhexyloxyphenol methoxyphenyl Triazine), as well as dibutyl adipate (INCI: Dibutyl adipate) and / or butylene glycol dicaprylate / dicaprate (INCI: Butylene Glycol Dicaprylate / Dicaprate).
[0002] 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.
[0003] 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.
[0004] Cosmetics typically contain a number of perfumes designed to mask unpleasant inherent odors of preparation ingredients and to give the cosmetic its individual, manufacturer-specific scent.
[0005] However, a disadvantage of the state of the art is that the perfume ingredient vanillin (4-hydroxy-3-methoxybenzaldehyde) tends to crystallize out of the cosmetic preparations in the presence of the UV light protection filter 2,4-bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis- Ethylhexyloxyphenol methoxyphenyl Triazine). These crystallization nuclei then in turn lead to the crystallization of other poorly soluble, lipophilic compounds, in particular the 2,4-bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis- Ethylhexyloxyphenol methoxyphenyl Triazine), so that not only the sensory properties of the preparation suffer from the crystal formation, but also the UV protection (especially the UV protection) of the affected cosmetic preparation is reduced or completely lost.
[0006] To suppress crystallization phenomena of lipophilic UV light filters, the oil component C is usually added. 12-15 Alkyl benzoate is used, a compound that is particularly suitable for keeping 2,4-Bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis- Ethylhexyloxyphenol methoxyphenyl Triazine) in solution in the oil phase.
[0007] However, a disadvantage of the state of the art is that in C 12-15 Alkyl benzoate precipitates vanillin from the preparation particularly quickly and thoroughly. It is therefore present in the combination of 4-hydroxy-3-methoxybenzaldehyde (INCI: vanillin), 2,4-bis-{[4-(2-ethylhexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: bis-ethylhexyloxyphenol methoxyphenyl triazine), and C 12-15 Alkyl benzoate (especially under the influence of light) leads to increased crystal formation, which should actually be prevented.
[0008] The object of the present invention was therefore to develop a combination of substances for cosmetic sunscreens that can be perfumed with vanillin without having to forgo (or use in a significantly reduced amount) the widely used UV filter 2,4-Bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis- Ethylhexyloxyphenol methoxyphenyl Triazine).
[0009] The problem is surprisingly solved by a cosmetic preparation containing 4-hydroxy-3-methoxybenzaldehyde (INCI: Vanillin). 2,4-Bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis-Ethylhexyloxyphenol methoxyphenyl Triazine), as well as Dibutyl adipate (INCI: Dibutyl adipate) and / or butylene glycol dicaprylate / dicaprate (INCI: Butylene Glycol Dicaprylate / Dicaprate).
[0010] According to the invention, it is advantageous if the preparation contains 4-hydroxy-3-methoxybenzaldehyde (INCI: Vanillin) in a concentration of 0.0002 to 1.5 wt%, based on the total weight of the preparation. The preferred concentration according to the invention is between 0.004 and 0.5 wt%, based on the total weight of the preparation.
[0011] Advantageous embodiments of the present invention are characterized in that the preparation contains 2,4-bis-{[4-(2-ethylhexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis-Ethylhexyloxyphenol methoxyphenyl Triazine) in a concentration of 0.5 to 9.5 wt%, based on the total weight of the preparation. The preferred concentration according to the invention is between 0.5 and 5.0 wt%, based on the total weight of the preparation.
[0012] The preparation according to the invention can be in three different versions: In the first version, the preparation contains a combination of 4-Hydroxy-3-methoxybenzaldehyde (INCI: vanillin), 2,4-Bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis-Ethylhexyloxyphenol methoxyphenyl Triazine) and Dibutyl adipate (INCI: Dibutyl adipate). In the second variant, the preparation contains a combination of 4-hydroxy-3-methoxybenzaldehyde (INCI: vanillin), 2,4-Bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis-Ethylhexyloxyphenol methoxyphenyl Triazine) and Butylene glycol dicaprylate / dicaprate (INCI: Butylene Glycol Dicaprylate / Dicaprate). In the third variant, the preparation contains a combination of 4-Hydroxy-3-methoxybenzaldehyde (INCI: vanillin), 2,4-Bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis-Ethylhexyloxyphenol methoxyphenyl Triazine), Dibutyl adipate (INCI: Dibutyl adipate) and Butylene glycol dicaprylate / dicaprate (INCI: Butylene Glycol Dicaprylate / Dicaprate).
[0013] In these cases, when dibutyl adipate (INCI: Dibutyl adipate) and butylene glycol dicaprylate / dicaprate (INCI: Butylene Glycol Dicaprylate / Dicaprate) are present, these compounds can be used advantageously in the following concentrations.
[0014] According to the invention, it is advantageous if the preparation contains dibutyl adipate (INCI: Dibutyl adipate) in a concentration of 0.5 to 10.0 wt%, based on the total weight of the preparation. The preferred concentration according to the invention is between 1.0 and 5.0 wt%, based on the total weight of the preparation.
[0015] Furthermore, according to the invention, it is advantageous if the preparation contains butylene glycol dicaprylate / dicaprate (INCI: Butylene Glycol Dicaprylate / Dicaprate) in a concentration of 0.5 to 10.0 wt%, based on the total weight of the preparation. The preferred concentration according to the invention is between 1.0 and 5.0 wt%, based on the total weight of the preparation.
[0016] Advantageous embodiments of the present invention are further characterized in that the preparation C 12-15 - Alkyl benzoate in a concentration of not more than 10% by weight, based on the total weight of the preparation.
[0017] In addition to 2,4-Bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis- Ethylhexyloxyphenol methoxyphenyl Triazine), the preparation according to the invention may contain further UV filters.
[0018] In particular, according to the invention, it is advantageous if the preparation contains (2-[-4-(Diethylamino)-2-hydroxybenzoyl] Benzoic acid hexyl ester (INCI: Diethylamino Hydroxybenzoyl Hexyl Benzoate), 2,4,6-Tris-[anilino-(p-carbo-2'-ethyl-1'-hexyloxy)]-1,3,5-triazine (INCI: Ethylhexyl Triazone) and / or 4-(tert-Butyl)-4'-methoxydibenzoylmethane (INCI Butyl Methoxydibenzoylmethane).
[0019] The preparation according to the invention contains (2-[-4-(Diethylamino)-2-hydroxybenzoyl] benzoic acid hexyl ester (INCI: Diethylamino Hydroxybenzoyl Hexyl Benzoate), this substance is advantageously used according to the invention in a concentration of 0.5 to 9.5 wt%, based on the total weight of the preparation.
[0020] If the preparation according to the invention contains 2,4,6-Tris-[anilino-(p-carbo-2'-ethyl-1'-hexyloxy)]-1,3,5-triazine (INCI: Ethylhexyl Triazone), this substance is advantageously used according to the invention in a concentration of 0.3 to 5.0 wt%, based on the total weight of the preparation.
[0021] The preparation according to the invention contains 4-(tert-Butyl)-4'-methoxydibenzoylmethane (INCI Butyl Methoxydibenzoylmethane), this substance is advantageously used according to the invention in a concentration of 1.0 to 5.0 wt%, based on the total weight of the preparation.
[0022] Furthermore, it is advantageous in the context of the present invention if the preparation contains ethylhexylglycerin. In such a case, the preparation according to the invention is preferably characterized in that the preparation contains ethylhexylglycerin in a concentration of 0.01 to 0.75% by weight, based on the total weight of the preparation.
[0023] According to the invention, the preparation can be in two different dosage forms: in the form of an ethanolic solution and in the form of an emulsion.
[0024] If the preparation is in the form of an ethanolic solution, the ethanol concentration is advantageously 30 to 55% by weight according to the invention, based on the total weight of the preparation.
[0025] If the preparation is in the form of an emulsion, it is also advantageous according to the invention if the preparation contains ethanol.
[0026] In general, if the preparation according to the invention contains ethanol, the advantageous embodiments according to the invention are characterized in that the preparation optionally contains ethanol in a concentration of 3 to 55% by weight, based on the total weight of the preparation.
[0027] Advantageous embodiments of the present invention are characterized in that the preparation is in the form of an emulsion and, preferably, in the form of an oil-in-water emulsion (O / W emulsion).
[0028] In such a case, it is advantageous according to the invention if the preparation contains one or more O / W emulsifiers selected from the group of compounds glyceryl stearate citrate, glyceryl stearate, glyceryl stearate (self-emulsifying), stearic acid, stearate salts, polyglyceryl-3 methylglycosederate, sodium cetearyl sulfate, potassium cetyl phosphate, polyglyceryl-6 stearate, polyglyceryl-6 behenate, polyglyceryl-10 stearate, sodium stearoyl glutamate, polyglyceryl-3 polyricinoleate (INCI: polyglyceryl-3 polyricinoleate), polyglyceryl-3 diisostearate and polyglyceryl-4 diisostearate / polyhydroxystearate / sebacate.
[0029] Furthermore, the advantageous embodiments according to the invention are characterized in that 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-methoxycinnamic acid 2-ethylhexyl ester (INCI: octyl methoxycinnamate), ethylhexyl 2-cyano-3,3-diphenyl acrylate (INCI: octocrylene), parabens (in particular methyl, propyl and butyl paraben), methylisothiazolinone, chloromethylisothiazolinone, DMDM hydantoin, mineral oils, mineral waxes and silicone oils.
[0030] However, it is advantageous in the sense of the present invention if the preparation contains one or more diols selected from the group of compounds 2-methyl-1,3-propanediol, propane-1,2-diol, butane-1,2-diol, pentane-1,2-diol, hexane-1,2-diol, octane-1,2-diol, decane-1,2-diol.
[0031] It is also advantageous according to the invention if the preparation contains one or more compounds selected from the group consisting of hexyl salicylate, 2-isobutyl-4-hydroxy-4-methyltetrahydropyran, further adipic acid diesters (other than dibutyl adipate), methylheptenone, alpha-isomethyl ionone, coumarin, hexyl cinnamal, limonene, linalool, diethyl succinate, hydroxyisohexyl 3-cyclohexene carboxaldehyde, menthyl PCA, citronellyl methyl crotonate, benzyl benzoate, benzyl alcohol, benzyl cinnamate, benzyl salicylate, citronellol, eugenol, and geraniol.
[0032] Furthermore, it is advantageous according to the present invention if the preparation contains 4-hydroxyacetophenone. In such a case, it is preferred according to the invention if the preparation contains 4-hydroxyacetophenone in a concentration of 0.1 to 0.5 wt%, based on the total weight of the preparation.
[0033] Furthermore, the cosmetic preparation according to the invention can contain the ingredients commonly used in cosmetics. comparative experiment
[0034] Four percent bis-ethylhexyloxyphenol methoxyphenyl triazine is dissolved in C12-15 alkyl benzoates at 80°C. Then, 0.5 percent vanillin is added at room temperature. This dissolved mixture is stored at room temperature and exposed to light. After two months of storage, distinct crystals have formed in the light pattern, which are also visible to the naked eye.
[0035] Three separate reactions were conducted, each containing 4% bis-ethylhexyloxyphenol methoxyphenyl triazine in dibutyl adipate, butylene glycol dicaprylate / dicaprate, and a 1:1 mixture of dibutyl adipate and butylene glycol dicaprylate / dicaprate, respectively, at 80°C. Subsequently, 0.5% vanillin was added at room temperature. These dissolved mixtures were stored at room temperature and exposed to light. Even after six months of storage, no crystals were visible in the light pattern. Examples
[0036] The following examples are intended to illustrate the present invention without limiting it. Unless otherwise stated, all quantities, proportions, and percentages are based on the weight and total quantity or total weight of the preparations. Beispiel1 Beispiel2 Beispiel3 Beispiel4 Beispiel5 INCI m [%] m [%] m [%] m [%] m [%] Bis-Ethylhexyloxyphenol MethoxyphenylTriazine 0,6 5 2 4 1,3 Hydroxyacetophenone 0,5 0,2 0,1 0,1 0 Ethylhexylglycerin 0,5 0,3 0,1 0,2 0 Dibutyl adipate 3 7 9 0 5 Butylene Glycol Dicaprylate / Dicaprate 7 3 0 9 5 C12-15 Alkyl Benzoate 2 10 5 7 10 Vanillin 0,4 0,003 0,5 0,0002 1 Diethylamino Hydroxybenzoyl HexylBenzoate 5 0 9,5 2 0,3 Ethylhexyl Triazone 5 0,3 3 0 0 Butyl Methoxydibenzoylmethane 1 5 0 4,5 2 Phenylbenzimidazole Sulfonic Acid 0,5 1,0 0 1,5 0 Diethylhexyl Butamido Triazone 1 3 0 2 0 Ethylhexyl Salicylate 5 0 0 3 5 Titanium Dioxide (nano) + Silica +Dimethicone 0 1,5 0 0 0 Glycerin + Aqua 10 5 7 7 7 Caprylyl Glycol 0 0 0,3 0 0 Alcohol Denat. 3 5 8 7,5 50 Sodium Hydroxide 0,076 0,153 0 0,229 0 Aqua Ad 100 Ad 100 Ad 100 Ad 100 Ad 100 Trisodium Ethylenediamine Disuccinate 0,5 0,4 0 0 0 Aqua + Trisodium EDTA 0 0 0,3 0,4 0 Cetearyl Alcohol 0,5 0 0 0 0 Hydroxypropyl Methylcellulose 0 0 0,5 0 0 Xanthan Gum 0,5 0,5 0 0,5 0 Hydroxypropyl Starch Phosphate 0,5 0 0 0 0 Behenyl Alcohol 0 0 0 0,5 0 Stearyl Alcohol 0 0 0,5 0 0 Cellulose Gum 0 0,2 0 0 0 Cetyl Alcohol 0 0 0,5 0 0 Microcrystalline Cellulose 0 0,1 0 0 0 Phenoxyethanol 0,2 0 0 0,5 0 Parfum 0,3 0 0,7 0 0,5 Diisostearoyl Polyglyceryl-3 DimerDilinoleate 0 0,5 1 0 0 Polyglyceryl-6 Stearate +Polyglyceryl-6 Behenate 2 0 0 0 0 Glyceryl Stearate 0 1 0,5 0 0 Sodium Stearoyl Glutamate 0 0,5 0 0 0 Polyglyceryl-10 Stearate 0 0 0 0,5 0 Sodium Cetearyl Sulfate 0 0 0 0,5 0 Polyglyceryl-3 Methylglucose Distearate 0 0 1 0 0 Glyceryl Stearate SE 0 0 0 0,5 0 Glyceryl Stearate Citrate 0 0 0,5 0 0 Dibutyl Adipate 1 4 2 0 3 Isopropyl Palmitate 3 2 4 5 5 Butylene Glycol Dicaprylate / Dicaprate 0 4 0 3 5 Dicaprylyl Carbonate 0 0 0 0 2 Copernicia Cerifera Cera 0 0 1 0 0 Propylene Glycol Dicaprylate / Dicaprate 5 0 2 0 5 Hydrogenated Rapeseed Oil 0,5 0 0 0 0 Cocoglycerides 0 0 4 0 0 Cetyl Palmitate 0 0 0 0,5 0 C18-38 Alkyl Hydroxystearoyl Stearate 0 0,5 0 0 0
Claims
[1] Cosmetic preparation containing 4-hydroxy-3-methoxybenzaldehyde (INCI: Vanillin), 2,4-bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis-Ethylhexyloxyphenol methoxyphenyl Triazine), and dibutyl adipate (INCI: Dibutyl adipate) and / or butylene glycol dicaprylate / dicaprate (INCI: Butylene Glycol Dicaprylate / Dicaprate). [2] Cosmetic preparation according to claim 1, characterized by , that the preparation contains 4-hydroxy-3-methoxybenzaldehyde (INCI: Vanillin) in a concentration of 0.0002 to 1.5 wt%, based on the total weight of the preparation. [3] Cosmetic preparation according to any one of the preceding claims, characterized by , that the preparation contains 2,4-Bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine (INCI: Bis- Ethylhexyloxyphenol methoxyphenyl Triazine) in a concentration of 0.5 to 9.5 wt%, based on the total weight of the preparation. [4] Cosmetic preparation according to any one of the preceding claims, characterized by that the preparation contains dibutyl adipate (INCI: Dibutyl adipate) in a concentration of 0.5 to 10% by weight, based on the total weight of the preparation. [5] Cosmetic preparation according to any one of the preceding claims, characterized by , that the preparation contains butylene glycol dicaprylate / dicaprate (INCI: Butylene Glycol Dicaprylate / Dicaprate) in a concentration of 0.5 to 10% by weight, based on the total weight of the preparation. [6] Cosmetic preparation according to any one of the preceding claims, characterized by that the preparation C 12-15 - Alkyl benzoate in a concentration of not more than 10% by weight, based on the total weight of the preparation. [7] Cosmetic preparation according to any one of the preceding claims, characterized by, that the preparation contains (2-[-4-(Diethylamino)-2-hydroxybenzoyl] Benzoic acid hexyl ester (INCI: Diethylamino Hydroxybenzoyl Hexyl Benzoate), 2,4,6-Tris-[anilino-(p-carbo-2'-ethyl-1'-hexyloxy)]-1,3,5-triazine (INCI: Ethylhexyl Triazone) and / or 4-(tert-Butyl)-4'-methoxydibenzoylmethane (INCI Butyl Methoxydibenzoylmethane). [8] Cosmetic preparation according to any one of the preceding claims, characterized by that the preparation contains ethylhexylglycerin. [9] Cosmetic preparation according to any one of the preceding claims, characterized by that the preparation contains ethylhexylglycerin in a concentration of 0.01 to 0.75% by weight, based on the total weight of the preparation. [10] Cosmetic preparation according to any of the preceding claims, characterized by that the preparation contains ethanol. [11] Cosmetic preparation according to any of the preceding claims, characterized bythat the preparation contains ethanol in a concentration of 3 to 55% by weight, based on the total weight of the preparation. [12] Cosmetic preparation according to any of the preceding claims, characterized by that the preparation is in the form of an emulsion and, preferably, in the form of an oil-in-water emulsion (O / W emulsion). [13] Cosmetic preparation according to any of the preceding claims, characterized by that the preparation contains one or more O / W emulsifiers selected from the group of compounds glyceryl stearate citrate, glyceryl stearate, glyceryl stearate (self-emulsifying), stearic acid, stearate salts, polyglyceryl-3 methylglycosederate, sodium cetearoyl sulfate, potassium cetyl phosphate, polyglyceryl-6 stearate, polyglyceryl-6 behenate, polyglyceryl-10 stearate, sodium stearoyl glutamate, polyglyceryl-3 polyricinoleate (INCI: polyglyceryl-3 polyricinoleate), polyglyceryl-3 diisostearate and polyglyceryl-4 diisostearate / polyhydroxystearate / sebacate. [14] Cosmetic preparation according to any of the preceding claims, characterized by that 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-methoxycinnamic acid 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. [15] Cosmetic preparation according to any of the preceding claims, characterized by that the preparation contains one or more diols selected from the group of compounds 2-methyl-1,3-propanediol, propane-1,2-diol, butane-1,2-diol, pentane-1,2-diol, hexane-1,2-diol, octane-1,2-diol, decane-1,2-diol. [16] Cosmetic preparation according to any of the preceding claims, characterized by that the preparation contains one or more compounds selected from the group consisting of hexyl salicylate, 2-isobutyl-4-hydroxy-4-methyltetrahydropyran, other adipic acid diesters (other than dibutyl adipate), methylheptenone, alpha-isomethyl ionone, coumarin, hexyl cinnamal, limonene, linalool, diethyl succinate, hydroxyisohexyl 3-cyclohexene carboxaldehyde, menthyl PCA, citronellyl methyl crotonate, benzyl benzoate, benzyl alcohol, benzyl cinnamate, benzyl salicylate, citronellol, eugenol, and geraniol. [17] Cosmetic preparation according to any of the preceding claims, characterized by that the preparation contains 4-hydroxyacetophenone. [18] Cosmetic preparation according to any of the preceding claims, characterized by that the preparation contains 4-hydroxyacetophenone in a concentration of 0.1 to 0.5 wt%, based on the total weight of the preparation.