DE102004027475B4 - 2-phenylethyl benzoate in cosmetic preparations and the use for foam reinforcement - Google Patents

Abstract

Foamy, or foamable cosmetic Preparations containing 2-phenylethyl benzoate and one or more UV filter substances from the group of triazine derivatives.

Description

The The present invention relates to foamy or foamable cosmetic Preparations containing 2-phenylethyl benzoate and one or more UV filter substances from the group of triazine derivatives

Foams or foamy Preparations belong to disperse systems.

The By far the most important and best known disperse system are emulsions Emulsions are two- or multi-phase systems of two or three more in each other not or only slightly soluble liquids. The liquids (pure or as solutions) lie in an emulsion in a more or less fine distribution which generally has only limited stability.

Foams are Structures made of gas-filled, spherical or polyhedron-shaped Cells caused by liquid, semi-liquid, highly viscous or fixed cell ridges. The cell bridges, connected via so-called nodal points, form a coherent one Framework. Between the cell bridges, the foam lamellae (closed-cell Foam). If the foam lamellae are destroyed or flow At the end of foaming back into the cell webs, one obtains an open-celled Foam. Also foams are thermodynamically unstable, since by reducing the surface surface energy can be won. The stability and thus the existence of a Foam is thus dependent on how far it is possible to prevent its self-destruction.

cosmetic foams are usually dispersed systems of liquids and gases, the liquid the dispersant and the gas are the dispersed substance. foams from low-viscosity liquids become temporary by surface-active Stabilized substances (surfactants, foam stabilizers). Such tenside foams because of their big ones inner surface a strong adsorption capacity, which exploited for example in cleaning and washing operations becomes. Accordingly, find cosmetic foams especially in the fields cleaning, such as shaving cream, and hair care Use.

to Generation of foam gas is blown into suitable liquids, or Foaming is achieved by vigorous beating, shaking, splashing or stirring the liquid in the gas atmosphere in question, provided that the fluids suitable surfactants or other surfactants (so-called Foaming agents) which, in addition to interfacial activity, also have some film-forming ability.

cosmetic foams have opposite Other cosmetic preparations have the advantage of being a fine one Allow distribution of active ingredients on the skin. However, they are cosmetic foams usually only by using special surfactants, which in addition often not tolerated by the skin are to reach.

One Disadvantage of the prior art is that such foams only are little stable, which is why they usually collapse within about 24 hours. A request to However, cosmetic preparations is that this one possible Years of stability have. This problem is generally taken into account by that the consumer the actual foam only at the application with the help of a suitable spraying system itself, for which, for example, spray cans can be used, in which a liquefied Compressed gas serves as a propellant gas. When opening the pressure valve escapes the propellant-liquid mixture through a fine nozzle, the propellant evaporates leaving a foam.

Also foaming Cosmetic preparations are known per se. They are initially in a flowable form from an aerosol container applied to the skin and develop after a short delay first there under the influence of the contained Nachschäummittels the actual Foam, for example a shaving cream. Post-foaming preparations are often in special embodiments like frothing Shaving gels or the like.

Of the The prior art also knows cosmetic preparations, which already foamed in the production and thereby in itself one enough high stability show up in ordinary Wrapped, stored and put on the market (see for example DE-100 63 340-A1, DE-100 63 341-A1 and DE-100 63 342-A1).

One Disadvantage of the preparations of the prior art, however often the quality of the foam, d. H. the foam is soft, coarse-bubble and after removal from the container only a little stable. Also foamable Cosmetic emulsions (so-called "aerosol foams") can be broken down the prior art without the use of special surfactants not formulate or produce technically. This applies in particular for systems, based on classic emulsifiers. According to the state of the art develop such systems with the addition of propellant exclusively aqueous humid foams, which break quickly after application.

task Thus, the present invention was to enrich the state of the art and cosmetic self-foaming and / or foamy Preparations available to provide that do not have the disadvantages of the prior art.

• • schaumförmige, oder schäumbare kosmetische Zubereitungen enthaltend 2-Phenylethylbenzoat und ein oder mehrere UV-Filtersubstanzen aus der Gruppe der Triazinderivate, sowie durch die
• • Verwendung von 2-Phenylethylbenzoat zur Schaumverstärkung und Schaumstabilisierung selbstschäumender, schaumförmiger, nachschäumender oder schäumbarer kosmetischer Zubereitungen enthaltend ein oder mehrere UV-Filtersubstanzen aus der Gruppe der Triazinderivate.

The task is solved by surprise

• Foam-like or foamable cosmetic preparations containing 2-phenylethyl benzoate and one or more UV filter substances from the group of triazine derivatives, and by the
• Use of 2-phenylethyl benzoate for foam reinforcement and foam stabilization of self-foaming, foam-like, post-foaming or foamable cosmetic preparations containing one or more UV filter substances from the group of the triazine derivatives.

Under "self-foaming", "foamy", "nachschäumend" or "foamable" is in the sense of Understand the present invention that the gas bubbles (arbitrary) distributed in one (or more) liquid phase (s), the preparations are not necessarily macroscopically Look like a foam. Cosmetic preparations according to the present invention (in hereinafter also referred to as foams for the sake of simplicity) can, for. B. macroscopically visible dispersed systems from in liquids represent dispersed gases. The foam character can but also, for example first under a (light) microscope visible. Furthermore are foams according to the present Invention - in particular then, when the gas bubbles too small to be detected under a light microscope - even on recognizable by the strong volume increase of the system.

By For the first time, the invention becomes a rich, compact cream foam ("Mousse") accessible, the over a long storage life as well as an extraordinarily high stability and a Compact appearance distinguishes. Compositions according to the invention are already developing during their production - for example while of stirring or in the homogenization - too fine bubble foams. According to the invention are fine bubbles, rich foams of outstanding cosmetic elegance available. Furthermore, according to the invention are particularly good skin-friendly Preparations available, with valuable ingredients distributed particularly well on the skin can be.

object The invention further relates to the use of 2-phenylethyl benzoate for reducing the bubble size of self-foaming, foamy, after-foaming or foamable cosmetic preparations.

With "foam reinforcement" is beyond meant that stability the foamed Preparations (the "foam stability") compared to otherwise same preparations which no UV filter substances according to the invention significantly improved, d. H. by the use according to the invention a break of the foams delayed in time.

Further is under "foam reinforcement" within the meaning of the present Invention to understand that the cosmetic properties the foams of the invention in comparison to preparations which do not contain UV filter substances according to the invention, be significantly improved: Thus obtained by the use of the invention rich, firm foams ("Foam creams"), which despite their Compactness and richness are easily redistributable and fast move in.

Especially is under "foam reinforcement" within the meaning of the present Invention to understand that the bubble size of the foams of the invention in comparison to preparations which do not contain UV filter substances according to the invention, is smaller. In contrast, the number of bubbles is increased in the same volume.

With "bubbles" are in the sense of present invention, the gas bubbles meant, under "bubble size" is accordingly the diameter of the gas bubbles to understand.

This Effect can be very good from a microscopic foam examination be clarified. The aim of this study is the microscopic Determination of the number and size of bubbles in cosmetic products.

• • Von der zu untersuchenden kosmetischen Zubereitung wird an drei verschiedenen Stellen (z. B. oben, Mitte, unten) aus dem Behälter jeweils eine Probe mittels Spatel entnommen (entsprechend drei Proben pro Zubereitung). (Aerosolschäume werden in ein Reservoir oder auf Zellstoff gesprüht und die Proben aus dem Reservoir gezogen.)
• • Einwaage von 9 mg ± 0,5mg auf Objektträgern
• • Abdeckung der Probe mit einem Abdeckglas
• • Vor der eigentlichen Aufnahme wird auf den Objektträger mit Abdeckglas für 15 sec ein Gewicht von 20 g gelegt.
• • Anschließend werden von jeder Probe drei Bilder aufgenommen, wobei die untersuchte Fläche 6,22 mm × 4,66 mm = 28,11 mm² beträgt. Dazu wird das Mikroskop auf 125fache Vergrößerung eingestellt und die Probe im Durchlicht beleuchtet (Digitalkamera Polaroid DMC und Bildanalyse-Programm KS400).

A microscopic foam examination can be carried out, for example, as follows, at a constant temperature of 21 ° C.:

• • One sample of the cosmetic preparation to be examined is taken from the container at three different locations (eg top, middle, bottom) using a spatula (corresponding to three samples per preparation). (Aerosol foams are sprayed into a reservoir or pulp and samples are drawn from the reservoir.)
• • Weighed 9 mg ± 0.5 mg on slides
• • Cover the sample with a cover glass
• • Before the actual recording, place a weight of 20 g on the slide with cover glass for 15 sec.
• • Subsequently, three images are taken of each sample, with the area under investigation being 6.22 mm × 4.66 mm = 28.11 mm ² . For this, the microscope is set to 125x magnification and the sample is illuminated in transmitted light (digital camera Polaroid DMC and image analysis program KS400).

Advantageous preparations according to the present invention have a mean bubble size of 0.005 to 0.5 mm ² , preferably from 0.005 to 0.2 mm ² , more preferably from 0.005 to 0.1 mm ² and a number of bubbles from 100 to 4000, preferably from 500 to 3000, particularly advantageously from 1000 to 3000, in each case based on the examined image section (see above).

• • Der Einsatz des erfindungsgemäßen 2-Phenylethylbenzoats führt zu einem besonders angenehmen samtig-seidigen Hautgefühl, so dass in den Zubereitungen auf den Einsatz von Cyclomethiconen verzichtet werden kann. Erfindungsgemäß vorteilhaft sind daher Cyclomethicon-freie kosmetische Zubereitungen.
• • Durch den Einsatz des erfindungsgemäßen 2-Phenylethylbenzoats lassen sich überraschend große Mengen an UV-Filtersubstanzen aus der Gruppe der Triazinderivate in der Zubereitung einarbeiten (lösen). Dadurch kann die Gesamtmenge an Ölkomponenten in der Zubereitung deutlich gesenkt werden, ohne das Einbußen bei der UV-Schutzleistung der Zubereitung in Kauf genommen werden müssen. Es lassen sich somit besonders fettarme („leichte") und wenig klebrige Zubereitungen mit hohem UV-Schutz herstellen, die sich insbesondere für die Gesichtspflege eignen.
• • Durch den Einsatz des erfindungsgemäßen 2-Phenylethylbenzoats lässt sich die Einsatzkonzentration von Konservierungsmitteln in der Zubereitung reduzieren.

In addition, the preparation according to the invention has further surprising advantages over the preparations of the prior art.

• The use of the 2-phenylethyl benzoate according to the invention leads to a particularly pleasant velvety-silky skin feel, so that the use of cyclomethicones can be dispensed with in the preparations. Therefore advantageous according to the invention are cyclomethicone-free cosmetic preparations.
• By using the 2-phenylethyl benzoate according to the invention, it is possible to incorporate (dissolve) surprisingly large amounts of UV filter substances from the group of the triazine derivatives in the preparation. As a result, the total amount of oil components in the preparation can be significantly reduced, without sacrificing the UV protection performance of the preparation must be taken into account. It is thus possible to prepare particularly low-fat ("light") and low-stick preparations with high UV protection, which are particularly suitable for facial care.
• The use of the 2-phenylethyl benzoate according to the invention makes it possible to reduce the use concentration of preservatives in the preparation.

The inventive preparation or uses according to the invention are advantageous according to the invention characterized in that it contains 2-phenylethyl benzoate in a concentration from 0.5 to 20% by weight and according to the invention preferably from 2 to 10% by weight, each based on the total weight of the preparation contains.

und ist beispielsweise unter dem Handelsnamen X-Tend^TM 226 bei der Firma ISP erhältlich.The 2-phenylethyl benzoate (INCI: 2-phenylethyl benzoate) according to the invention has the following structure

and is available, for example, under the trade name X-Tend ^™ 226 from ISP.

• • 2,4-Bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazin (INCI: Aniso Triazin, erhältlich unter dem Handelsnamen Tinosorb S),
• • Dioctylbutylamidotriazon (INCI: Dioctylbutamidotriazone),
• • 2,4-bis-[5-1(dimethylpropyl)benzoxazol-2-yl-(4-phenyl)-imino]-6-(2-ethylhexyl)-imino-1,3,5-triazin mit der (CAS Nr. 288254-16-0, erhältlich bei 3V Sigma unter der Handelsbezeichnung Uvasorlb^® K2A),
• • 4,4',4''-(1,3,5-Triazin-2,4,6-triyltrümino)-tris-benzoesäure-tris(2-ethylhexylester) (auch: 2,4,6-Tris-[anilino-(p-carbo-2'-ethyl-1'-hexyloxy)]-1,3,5-triazin (INCI: Octyl Triazone), welches von der BASF Aktiengesellschaft unter der Warenbezeichnung UVINUL^® T 150 vertrieben wird).

According to the invention, the preparation or uses according to the invention are advantageously characterized in that the preparation contains one or more UV filter substances from the group of triazine derivatives selected from the group of the compounds

• 2,4-bis - {[4- (2-ethyl-hexyloxy) -2-hydroxy] -phenyl} -6- (4-methoxyphenyl) -1,3,5-triazine (INCI: aniso triazine, available at the trade name Tinosorb S),
• Dioctylbutylamidotriazone (INCI: dioctylbutamidotriazone),
• • 2,4-bis- [5-1 (dimethylpropyl) benzoxazol-2-yl- (4-phenyl) -imino] -6- (2-ethylhexyl) -imino-1,3,5-triazine with the (CAS no. 288254-16-0, available from 3V Sigma under the trade designation Uvasorlb ^® K2A)
• • 4,4 ', 4''- (1,3,5-triazine-2,4,6-triyltrimino) tris-benzoic acid tris (2-ethylhexyl ester) (also: 2,4,6-tris [ anilino- (p-carbo-2'-ethyl-1'-hexyloxy)] - 1,3,5-triazine (INCI: octyl Triazone), which is sold by BASF Aktiengesellschaft under the trade name Uvinul ^® T 150).

wobei R¹, R² und R³ unabhängig voneinander gewählt werden aus der Gruppe der verzweigten und unverzweigten Alkylgruppen mit 1 bis 10 Kohlenstoffatomen bzw. ein einzelnes Wasserstoffatom darstellen. Erfindungsgemäß besonders bevorzugt ist das 2,4-Bis-{[4-(2-Ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazin (INCI: Bis-Ethylhexyloxylphenol Methoxyphenyl Triazin), welches unter der Handelsbezeichnung Tinosorb^® S bei der CIBA-Chemikalien GmbH erhältlich ist. Ein weiteres bevorzugtes Bis- Resorcinyltriazinderivat ist das 2-[4,6-Bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(octyloxy)phenol (CAS Nr.: 2725-22-6).The triazine derivatives which are advantageous according to the invention also include bis-resorcinyl triazine derivatives. They are characterized by the following structural formula:

wherein R ¹ , R ² and R ^{3 are} independently selected from the group of branched and unbranched alkyl groups having 1 to 10 carbon atoms or represent a single hydrogen atom. Particularly preferred according to the invention is 2,4-bis - {[4- (2-ethyl-hexyloxy) -2-hydroxy] -phenyl} -6- (4-methoxyphenyl) -1,3,5-triazine (INCI: Bis , which is available under the trade name Tinosorb ^® S from CIBA-Chemikalien GmbH -Ethylhexyloxylphenol methoxyphenyl triazine). Another preferred bis-resorcinyl triazine derivative is 2- [4,6-bis (2,4-dimethylphenyl) -1,3,5-triazin-2-yl] -5- (octyloxy) phenol (CAS No .: 2725- 22-6).

The Total amount of one or more bis-resorcinyl triazine derivatives in the finished cosmetic preparations is advantageous the range 0.01 wt .-% to 20 wt .-%, preferably from 0.1 to 10 % By weight selected, in each case based on the total weight of the preparations.

According to the invention preferred is the use of 2,4-bis - {[4- (2-ethyl-hexyloxy) -2-hydroxy] -phenyl} -6- (4-methoxyphenyl) -1,3,5-triazine as UV filter substance from the group of triazine derivatives.

According to the invention advantageous embodiments The present invention is characterized in that UV filter substances from the group of triazine derivatives in one Concentration of 0.01 to 20% by weight, based on the total weight the preparation contains. In this case, a content of UV filter substances from the group of triazine derivatives in a concentration of 0.5 to 10% by weight, based on the Total weight of the preparation, preferred according to the invention.

It is advantageous according to the invention if the preparation or use according to the present invention, contains additional UV filter substances.

advantageous further UV filter substances in the context of the present invention are those mentioned below, which are in the water and / or the oil phase may be present.

Advantageous UV filter substances which are liquid at room temperature for the purposes of the present invention are 2-ethylhexyl 2-cyano-3,3-diphenylacrylate (INCI: octocrylene) and esters of cinnamic acid, preferably 2-ethylhexyl 4-methoxycinnamate (2-ethylhexyl) Ethylhexyl 4-methoxycinnamate, INCI: octyl methoxycinnamate) and isopentyl 4-methoxycinnamate (isopentyl 4-methoxycinnamate, INCI: isoamyl p-methoxycinnamate), 3- (4- (2,2-bis ethoxycarbonylvinyl) phenoxy) propenyl) methoxysiloxane / Dimethylsiloxane copolymer, which is available, for example, under the trade name Parsol ^® SLX from Hoffmann La Roche.

Advantageous UV-A filter substances for the purposes of the present invention are dibenzoylmethane derivatives, in particular 4- (tert-butyl) -4'-methoxydibenzoylmethane (CAS-Nr. 70356-09-1), marketed by Givaudan under the trade name Parsol ^® 1789 and is sold by Merck under the trade name Eusolex ^® 9020th

worin
R¹ und R² unabhängig voneinander Wasserstoff, C₁-C₂₀-Alkyl, C₃-C₁₀-Cycloalkyl oder C₃-C₁₀-Cycloalkenyl bedeuten, wobei die Substituenten R¹ und R² gemeinsam mit dem Stickstoffatom, an das sie gebunden sind, einen 5- oder 6-Ring bilden können und
R³ einen C₁-C₂₀-Alkyl Rest bedeutet.Further advantageous UV-A filter substances in the context of the present invention are hydroxybenzophenones, which are distinguished by the following structural formula:

wherein
R ¹ and R ² independently of one another are hydrogen, C ₁ -C ₂₀ -alkyl, C ₃ -C ₁₀ -cycloalkyl or C ₃ -C ₁₀ -cycloalkenyl, where the substituents R ¹ and R ² together with the nitrogen atom to which they are attached are bound, can form a 5- or 6-ring and
R ^{3 is} a C ₁ -C ₂₀ -alkyl radical.

und unter dem Uvinul A Plus bei der Fa. BASF erhältlich ist.A particularly advantageous hydroxybenzophenone in the context of the present invention is 2- (4'-diethylamino-2'-hydroxybenzoyl) -benzoic acid hexyl ester (also: aminobenzophenone), which has the following structure:

and Uvinul A Plus is available from BASF.

• • Phenylen-1,4-bis-(2-benzimidazyl)-3,3'-5,5'-tetrasulfonsäure und ihre Salze, besonders die entsprechenden Natrium-, Kalium- oder Triethanolammonium-Salze, insbesondere das Phenylen-1,4-bis-(2-benzimidazyl)-3,3'-5,5'-tetrasulfonsäure-bis-natriumsalz mit der INCI-Bezeichnung Bisimidazylate (CAS-Nr.: 180898-37-7), welches beispielsweise unter der Handelsbezeichnung Neo Heliopan AP bei Haarmann & Reimer erhältlich ist;
• • Salze der 2-Phenylbenzimidazol-5-sulfonsäure, wie ihr Natrium-, Kalium- oder ihr Triethanolammonium-Salz sowie die Sulfonsäure selbst mit der INCI Bezeichnung Phenylbenzimidazole Sulfonsäure (CAS.-Nr. 27503-81-7), welches beispielsweise unter der Handelsbezeichnung Eusolex 232 bei Merck oder unter Neo Heliopan Hydro bei Haarmann & Reimer erhältlich ist;
• • 1,4-di(2-oxo-10-Sulfo-3-bornylidenmethyl)-Benzol (auch: 3,3'-(1,4-Phenylendimethylene)bis-(7,7-dimethyl-2-oxo-bicyclo-[2.2.1]hept-1-ylmethan Sulfonsäure) und dessen Salze (besonders die entprechenden 10-Sulfato-verbindungen, insbesondere das entsprechende Natrium-, Kalium- oder Triethanolammonium-Salz), das auch als Benzol-1,4-di(2-oxo-3-bornylidenmethyl-10-sulfonsäure) bezeichnet wird. Benzol-1,4-di(2-oxo-3-bornylidenmethyl-10-sulfonsäure) hat die INCI-Bezeichnung Terephtalidene Dicampher Sulfonsäure (CAS.-Nr.: 90457-82-2) und ist beispielsweise unter dem Handelsnamen Mexoryl SX von der Fa. Chimex erhältlich;
• • Sulfonsäure-Derivate des 3-Benzylidencamphers, wie z. B. 4-(2-Oxo-3-bornylidenmethyl)benzolsulfonsäure, 2-Methyl-5-(2-oxo-3-bornylidenmethyl)sulfonsäure und deren Salze.

Advantageous further UV filter substances in the context of the present invention are sulfonated, water-soluble UV filters, such as. B .:

• Phenylene-1,4-bis (2-benzimidazyl) -3,3'-5,5'-tetrasulfonic acid and its salts, especially the corresponding sodium, potassium or triethanolammonium salts, especially the phenylene-1,4 bis (2-benzimidazyl) -3,3'-5,5'-tetrasulfonic acid bis-sodium salt with the INCI name Bisimidazylate (CAS No .: 180898-37-7), which is available, for example, under the trade name Neo Heliopan AP is available from Haarmann &Reimer;
• Salts of 2-phenylbenzimidazole-5-sulfonic acid, such as its sodium, potassium or triethanolammonium salt, and the sulfonic acid itself with the INCI name phenylbenzimidazole sulfonic acid (CAS No. 27503-81-7), which is available, for example, from Trade name Eusolex 232 available from Merck or Neo Heliopan Hydro from Haarmann &Reimer;
• 1,4-di (2-oxo-10-sulfo-3-bornylidenemethyl) benzene (also: 3,3 '- (1,4-phenylenedimethylene) bis (7,7-dimethyl-2-oxo-bicyclo - [2.2.1] hept-1-ylmethane sulfonic acid) and its salts (especially the entprechenden 10-sulfato compounds, especially the corresponding sodium, potassium or triethanolammonium salt), which is also known as benzene-1,4-di Benzene-1,4-di (2-oxo-3-bomylidenemethyl-10-sulfonic acid) has the INCI name Terephtalidene Dicampher sulfonic acid (CAS No. N, 2-oxo-3-bionylidenemethyl-10-sulfonic acid). : 90457-82-2) and is available, for example, under the trade name Mexoryl SX from Chimex;
• Sulfonic acid derivatives of 3-Benzylidencamphers, such as. B. 4- (2-oxo-3-bomylidenemethyl) benzenesulfonic acid, 2-methyl-5- (2-oxo-3-bomylidenemethyl) sulfonic acid and salts thereof.

advantageous UV filter substances in the context of the present invention are further so-called broadband filters, i. Filter substances containing both UV-A as well as absorb UV-B radiation.

An advantageous broadband filter for the purposes of the present invention is also the 2,2'-methylenebis (6- (2H-benzotriazol-2-yl) -4- (1,1,3,3-tetramethylbutyl) phenol), which is available under the trade name Tinosorb ^® M from CIBA-Chemikalien GmbH.

Favorable Broadband filter according to the present invention is also the 2- (2H-benzotriazol-2-yl) -4-methyl-6- [2-methyl-3- [1,3,3,3-tetramethyl-1 - [(trimethylsilyl) oxy] disiloxanyl] propyl] phenol (CAS No .: 155633-54-8) with the INCI name Drometrizole Trisiloxane.

• • 3-Benzylidencampher-Derivate, vorzugsweise 3-(4-Methylbenzyliden)campher, 3-Benzylidencampher;
• • 4-Aminobenzoesäure-Derivate, vorzugsweise 4-(Dimethylamino)-benzoesäure(2-ethylhexyl)ester, 4-(Dimethylamino)benzoesäureamylester;
• • Ester der Benzalmalonsäure, vorzugsweise 4-Methoxybenzalmalonsäuredi(2-ethylhexyl)ester;
• • Dioctylbutylamidotriazon (INCI: Diethylhexyl Butamido Triazone), welches unter der Handelsbezeichnung UVASORB HEB bei Sigma 3V erhältlich ist;
• • Ester der Zimtsäure, vorzugsweise 4-Methoxyzimtsäure(2-ethylhexyl)ester, 4-Methoxyzimtsäureisopentylester;
• • Derivate des Benzophenons, vorzugsweise 2-Hydroxy-4-methoxybenzophenon, 2-Hydroxy-4-methoxy-4'-methylbenzophenon, 2,2'-Dihydroxy-4-methoxybenzophenon sowie
• • an Polymere gebundene UV-Filter.

The other UV filter substances can be oil-soluble or water-soluble. Advantageous oil-soluble filter substances are z. B .:

• 3-benzylidene camphor derivatives, preferably 3- (4-methylbenzylidene) camphor, 3-benzylidene camphor;
• 4-aminobenzoic acid derivatives, preferably 2-ethylhexyl 4- (dimethylamino) benzoate, 4- (dimethylamino) benzoic acid amyl ester;
• Esters of benzalmalonic acid, preferably di-2-ethylhexyl 4-methoxybenzalmalonate;
• Dioctylbutylamidotriazone (INCI: diethylhexyl butamido triazone), which is available under the trade name UVASORB HEB from Sigma 3V;
• Esters of cinnamic acid, preferably 4-methoxycinnamic acid (2-ethylhexyl) ester, 4-methoxycinnamic acid isopentyl ester;
• Derivatives of benzophenone, preferably 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4'-methylbenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone and
• • polymer-bound UV filters.

• • Phenylen-1,4-bis-(2-benzimidazyl)-3,3'-5,5'-tetrasulfonsäure-bis-natriumsalz (INCI: Bisimidazylate, Handelsname: Neoheliopan AP),
• • Dioctylbutylamidotriazon (INCI: Diethylhexyl Butamido Triazone, Handelsname: Uvasorb HEB),
• • 2-(4'-Diethylamino-2'-hydoxybenzoyl)-benzoesäurehexylester (auch: Aminobenzophenon) (INCI: Diethylamino Hydroxybenzoyl Hexyl Benzoat, Handelsname: Uvinul A plus),
• • (3Z)-1,7,7-trimethyl-3-(4-methylbenzylidene)bicyclo[2.2.1]heptan-2-one (INCI: 4-Methylbenzylidene Campher, Handelsname: Eusolex 6300),
• • 2-Ethylhexyl-2-cyano-3,3-diphenylacrylat (INCI: Octocrylene, Handelsname: Uvinul N-539),
• • Benzol-1,4-di(2-oxo-3-bornylidenmethyl-10-sulfonsäure) (INCI: Terephtalidene Dicampher Sulfonsäure, Handelsname: Mexoryl SX),
• • 2-(2H-benzotriazol-2-yl)-4-methyl-6-[2-methyl-3-[1,3,3,3-tetramethyl-1-[(trimethylsilyl)oxy]disiloxanyl]propyl]-phenol (INCI: Drometrizole Trisiloxane, Handelsname: Mexoryl XL).

Particularly advantageous UV filter substances are:

• Phenylene-1,4-bis (2-benzimidazyl) -3,3'-5,5'-tetrasulfonic acid bis-sodium salt (INCI: bisimidazylate, trade name: Neoheliopan AP),
• Dioctylbutylamidotriazone (INCI: diethylhexyl butamido triazone, trade name: Uvasorb HEB),
• • 2- (4'-diethylamino-2'-hydroxybenzoyl) -benzoic acid hexyl ester (also: aminobenzophenone) (INCI: diethylamino hydroxybenzoyl hexyl benzoate, trade name: Uvinul A plus),
• • (3Z) -1,7,7-trimethyl-3- (4-methylbenzylidenes) bicyclo [2.2.1] heptan-2-one (INCI: 4-methylbenzylidenes camphor, trade name: Eusolex 6300),
• 2-ethylhexyl-2-cyano-3,3-diphenylacrylate (INCI: Octocrylene, trade name: Uvinul N-539),
• Benzene-1,4-di (2-oxo-3-bomylidenemethyl-10-sulfonic acid) (INCI: Terephtalidene dicampher sulfonic acid, trade name: Mexoryl SX),
• 2- (2H-benzotriazol-2-yl) -4-methyl-6- [2-methyl-3- [1,3,3,3-tetramethyl-1 - [(trimethylsilyl) oxy] disiloxanyl] propyl] - phenol (INCI: Drometrizole Trisiloxane, trade name: Mexoryl XL).

• • 2-Ethylhexyl-4-methoxycinnamat (INCI: Octyl Methoxycinnamat, Handelsname: Parsol MCX),
• • 4-(tert.-Butyl)-4'-methoxydibenzoylmethan (INCI: Butylmethoxydibenzoylmethan, Handelsname: Parsol 1789),
• • Salze der 2-Phenylbenzimidazol-5-sulfonsäure, wie ihr Natrium-, Kalium- oder ihr Triethanolammonium-Salz sowie die Sulfonsäure selbst mit der INCI Bezeichnung Phenylbenzimidazole Sulfonsäure (Handelsname: Eusolex 232).

Very particularly advantageous UV filter substances in the context of the present invention are:

• 2-ethylhexyl-4-methoxycinnamate (INCI: octyl methoxycinnamate, trade name: Parsol MCX),
• 4- (tert-butyl) -4'-methoxydibenzoylmethane (INCI: butylmethoxydibenzoylmethane, trade name: Parsol 1789),
• Salts of 2-phenylbenzimidazole-5-sulfonic acid, such as its sodium, potassium or its triethanolammonium salt and the sulfonic acid itself with the INCI name phenylbenzimidazole sulfonic acid (trade name: Eusolex 232).

These additional UV filter substances can According to the invention advantageous in a total concentration of 0.01 to 20% by weight and preferred according to the invention in a total concentration of 0.5 to 10% by weight, respectively based on the total weight he preparation contained in this be.

• A. mindestens einem Emulgator A, gewählt aus der Gruppe der ganz-, teil- oder nicht neutralisierten, verzweigten und/oder unverzweigten, gesättigten und/oder ungesättigten Fettsäuren mit einer Kettenlänge von 10 bis 40 Kohlenstoffatomen,
• B. mindestens einem Emulgator B, gewählt aus der Gruppe der polyethoxylierten Fettsäureester mit einer Kettenlänge von 10 bis 40 Kohlenstoffatomen und mit einem Ethoxylierungsgrad von 5 bis 100 und
• C. mindestens einem Coemulgator C, gewählt aus der Gruppe der gesättigten und/oder ungesättigten, verzweigten und/oder unverzweigten Fettalkohole mit einer Kettenlänge von 10 bis 40 Kohlenstoffatomen besteht.

Particularly advantageous preparations according to the present invention contain an emulsifier system which consists of

• A. at least one emulsifier A selected from the group of fully, partially or not neutralized, branched and / or unbranched, saturated and / or unsaturated fatty acids having a chain length of from 10 to 40 carbon atoms,
• B. at least one emulsifier B, selected from the group of polyethoxylated fatty acid esters having a chain length of 10 to 40 carbon atoms and having a degree of ethoxylation of 5 to 100 and
• C. at least one co-emulsifier C, selected from the group of saturated and / or unsaturated, branched and / or unbranched fatty alcohols having a chain length of 10 to 40 carbon atoms.

Of the or the emulsifiers A are preferably selected from the group of fatty acids which are completely or partly with usual Alkalis (such as, for example, sodium and / or potassium hydroxide, sodium and / or Potassium carbonate and mono- and / or triethanolamine) neutralized are. For example, stearic acid and are particularly advantageous Stearates, isostearic acid and isostearates, palmitic acid and palmitates as well as myristic acid and myristates.

Of the or the emulsifiers B are preferably selected from the following group: PEG-9 stearate, PEG-8 distearate, PEG-20 stearate, PEG-8 stearate, PEG-8 oleate, PEG-25 Glycenltrioleat, PEG-40 sorbitan lanolate, PEG-15 glyceryl ricinoleate, PEG-20 glyceryl stearate, PEG-20 glyceryl isostearate, PEG-20 glyceryl oleate, PEG-20 stearate, PEG-20 methyl glucose sesquistearate, PEG-30 glyceryl isostearate, PEG-20 glyceryl laurate, PEG-30 stearate, PEG-30 glyceryl stearate, PEG-40 stearate, PEG-30 glyceryl laurate, PEG-50 stearate, PEG-100 stearate, PEG-150 laurate. For example, polyethoxylated are particularly advantageous Stearic.

The co-emulsifier (s) C are preferably chosen according to the invention from the following group: behenyl alcohol (C ₂₂ H ₄₅ OH), cetearyl alcohol [a mixture of cetyl alcohol (C ₁₆ H ₃₃ OH) and stearyl alcohol (C ₁₈ H ₃₇ OH)], lanolin alcohols (wool wax alcohols representing the unsaponifiable alcohol fraction of the wool wax obtained after saponification of wool wax). Particularly preferred are cetyl and cetylstearyl alcohol.

It is advantageous according to the invention the weight ratios from emulsifier A to emulsifier B to co-emulsifier C (A: B: C) as well a: choose b: c, where a, b and c are independent rational numbers from 1 to 5, preferably from 1 to 3 can represent. Particularly preferred is a weight ratio of about 1: 1: 1.

It is advantageous in the context of the present invention, the total amount the emulsifiers A and B and the co-emulsifier C from the range of 2 to 20 wt .-%, advantageously from 5 to 15 wt .-%, in particular of 7 to 13 wt .-%, each based on the total weight of the formulation, to choose.

It is optionally advantageous, although not necessary, if the formulations according to the present Invention contain further emulsifiers. Preferably, such To use emulsifiers, which for the production of W / O emulsions are suitable, these both individually and in any combination can exist with each other.

Prefers be the other emulsifiers or in the sense of the present Invention selected from the group of hydrophilic emulsifiers. Particularly according to the invention preferred are mono-, di-, triflic acid esters of sorbitan.

The Total amount of other emulsifiers is inventively advantageous less than 5% by weight, based on the total weight of the formulation, selected.

The List of the other emulsifiers mentioned, within the meaning of the present Invention can be used should of course not limiting.

Especially advantageous preparations in the context of the present invention free of mono- or diglyceryl fatty acid esters. Especially preferred are preparations according to the invention, which does not contain glyceryl stearate, glyceryl isostearate, glyceryl diisostearate, Glyceryl oleate, glyceryl palmitate, glyceryl myristate, glyceryl lanolate and / or glyceryl laurate.

The oil phase of preparations according to the invention is chosen favorably from the group of polar lipids with a polarity ≤ 35 mN / m Especially Advantageous lipids in the context of the present invention are all native lipids, such as. Olive oil, Sunflower oil, Soybean oil, Peanut oil, rapeseed oil, almond oil, palm oil, coconut oil, castor oil, wheat germ oil, grapeseed oil, thistle oil, evening primrose oil, macadamia nut oil, corn oil, avocado oil and the like as well as those listed below.

It is very particularly advantageous in the context of the present invention, one or more UV filter substances for foam reinforcement of self-foaming, foamy, after-foaming or foamable to use cosmetic preparations containing butylenes glycol Caprylates / caprates, C12-15 alkyl benzoates and / or di-C12 / 13 alkyl Tartrate included.

From The hydrocarbons are especially paraffin oil as well other hydrogenated polyolefins such as hydrogenated polyisobutenes, squalane and squalene to be used advantageously within the meaning of the present invention.

The Content of the lipids is advantageously less than 50 wt .-%, preferably between 1 and 40 wt .-%, particularly preferably between 5 and 15 wt .-%, each based on the total weight of the foamable Preparation.

If the lipid phase oil-soluble UV filter substances contains it is advantageous the content of the lipid phase less than 80 wt .-% to choose, preferably between 1 and 40 wt .-%, particularly preferably between 5 and 30 wt .-%, each based on the total weight of the foamable Preparation.

It may optionally be advantageous, although not mandatory is when the oil phase the preparations in the context of the present invention also non-polar Contains lipids.

The cosmetic according to the invention Preparations can as usual be composed. Particularly advantageous in the sense of the present Invention are preparations for the care of the skin: they can the cosmetic sunscreen, furthermore for cleaning or care of the skin and / or the hair and as a make-up product in decorative cosmetics serve. A further advantageous embodiment of the present invention Invention consists in after-sun products.

According to their structure, cosmetic compositions according to the present invention, for example, be used as a skin protection cream, day cream or night cream, etc. It is possible and advantageous, if appropriate, the compositions of the invention as a basis for pharma to use ceutical formulations.

As well like emulsions of liquid and solid consistency as cosmetic cleansing lotions or cleansing creams Can find use also represent the preparations according to the invention "cleaning foams", which for example, to remove make-up and / or makeup or as a mild wash foam - if necessary also for impure skin - used can be. Such cleaning foams can also advantageous as so-called "rinse often" preparations which are rinsed off the skin after use

The cosmetic according to the invention Preparations can also advantageous in the form of a foam for the care of the hair or the scalp, in particular a foam for insertion hair, a foam used to blow hair, a Frisierschaums.

It is also advantageous in the context of the present invention, cosmetic Preparing preparations whose main purpose is not protection is sunlight, but still contains a content of UV-protective substances contain. So z. In day creams or make-up products usually Incorporated UV-A or UV-B filter substances. Also, UV protectors, as well as antioxidants and, if desired, preservatives, effective protection of the preparations themselves against spoilage. Cheap are also cosmetic preparations in the form of a sunscreen available.

to Application are the cosmetic preparations according to the invention in the for Cosmetics usual Applied to the skin and / or hair in sufficient quantity.

The cosmetic agent according to the invention can for example, from aerosol containers removed and foamed become. Aerosol containers according to the invention are sprayers with a filling from the liquid or mushy substances that are under the pressure of a propellant stand (compressed gas or aerosol packs). Deratige containers can with Valves of very different design, which are the Remove the contents as foam.

Further can be advantageous the preparations according to the present invention Invention of propellant-free, mechanically operated pump atomizers (pump dispensers) be removed. Particularly advantageous in the sense of the present Invention are pumping systems, which without compressed gas, but with a Filter that causes special turbulence work.

The cosmetic preparations according to the invention can further preferably, for example, taken from Zweikammeraerosolbehältern and applied to the skin. According to the invention advantageous Packaging means are containers, in which a chamber with a filling of the liquid or mushy preparations under pressure one in a second Chamber located stationary primary propellant is located. such container can be equipped with valves of very different design, the the removal of the contents of the first chamber as an emulsion or gel in every situation - too with the valve down - allow.

An advantageous embodiment Bičan ^® -Aerosolbehälter in which the product is enclosed in a flexible bag made of metal or plastic inside the can.

Post-foaming compositions according to the invention do not froth, ie immediately after exiting an aerosol container, two or multiphase systems - in usually emulsions - dar. You can already by light rubbing, for example in the hands or when applying and rubbing on the skin, but also by stirring or other frothing processes to foams designed become.

It has about it out in surprising Way, that when using (secondary) propellants, particularly advantageous of propellants which are soluble in the optionally present oil phase, for example, usual Propane-butane mixtures, the inventive preparations not easy as aerosol droplets sprayed but to fine-bubble, develop rich foams, as soon as loaded with such (secondary) propellants Systems experience pressure relaxation.

When using hydrocarbons or mixtures thereof with 4 or 5 carbon atoms, In particular isobutane, n-pentane and isopentane, as (secondary) propellant can delay the self-foaming after exiting the pressure pack.

By the evaporation of the secondary blowing agent In the applied cosmetic product, the skin is further deprived of heat and a pleasant cooling effect obtained. Such nachschäumenden Preparations are therefore also considered advantageous embodiments the present invention with independent inventive step considered.

When Compressed gas containers come in the sense of the present invention mainly cylindrical Vessels of metal (Aluminum, tinplate, Content <1000 mL), protected or non-splitting Glass or plastic (content <220 mL) or splintering glass or plastic (capacity <150 mL), their selection pressure and fracture resistance, corrosion resistance, easy filling, if necessary sterilisability etc., but also aesthetic aspects, Handiness, printability etc. play a role. The maximum allowed Operating pressure of spray cans made of metal at 50 ° C is 12 bar and the maximum filling volume at this temperature about 90% of the total volume. For glass and plastic cans are considered lower, from the container size and the Propellants (whether liquefied, compacted or dissolved Gas) dependent Values for the operating pressure.

Especially advantageous in the context of the present invention are tinplate cans, Aluminum and glass. For corrosion protection reasons, metal cans can be painted inside be (silver or gold painted), including all commercially available Interior protective lacquers are suitable. Preferably in the sense of the present Invention are polyester, Epoxyphenol- and Polyamidimidlacke. Also film laminations of polyethylene (PE), polypropylene (PP) and / or Polyethylene terephthalate (PET) inside cans are beneficial, especially for Tinplate cans.

The Compressed gas containers are common one or two, but usually three-part cylindrical, conical or otherwise shaped. If plastics are used as spray container material, so These chemicals and sterilization temperature-resistant, gas-tight, impact resistant and against internal pressures over 12 bar be stable. In principle for The spray container purposes suitable are polyacetals and polyamides.

Of the internal construction of spray cans as well as the valve construction are depending on the purpose of use and the physical Nature of content - eg. B. whether as a two- or three-phase system - very varied and can from Professional by simply trying it out without inventive intervention be determined. For suitable embodiments be on the "aerosol Technology Handbook of Aersosol Packaging "(Wolfgang Tauscher, Melcher Verlag GmbH Heidelberg / Munich, 1996).

According to the invention advantageous valves may be formed with or without riser. The individual parts of which valves according to the invention are usually constructed preferably consist of the following materials: Plate: Tinplate: bright, gold or clear lacquered, laminated (PE, PP or PET) Aluminum: bright, silver or gold lacquered, different lacquer variants, Stoner-Mudge version Poetry: natural or synthetic elastomers or thermoplastic (sleeve Gaskets, foil-laminated from PE or PP) inner and outer seals, eg. B. from Perbunan, Buna, neoprene, butyl, CLB, LDPE, Viton, EPDM, chlorobutyl, bromobutyl and / or various compounds Bullet: PA, POM, brass and various special materials, standard bores (eg: 0.25 to 0.70 mm or 2 x 0.45 to 2 x 1.00 mm), different shank diameters

Feather: Metal, most preferably V2A, stainless steel; Plastic and also elastomer Casing: default and impact VPH holes, RPT holes or slotted for overhead applications Materials: z. As polyacetal, PA, PE, POM and the like Riser:  plastic (Polymer Resin), e.g. PE, PP, PA or polycarbonate

advantageous Spray heads in the sense For example, in the present invention, foam heads are upright Application (hold can vertically) or foam heads for overhead application with one or more several channels.

When Propellants are the usual "classic" volatiles, liquefied Propellant gases, such as dimethyl ether (DME) and / or linear or branched chain hydrocarbons having two to five carbon atoms (in particular ethane, propane, butane, isobutane and / or pentane) suitable, which are used alone or in mixture with each other can.

Also compressed air and other gases under pressure such as air, oxygen, nitrogen, hydrogen, helium, krypton, xenon, radon, argon, nitrous oxide (N ₂ O) and carbon dioxide (CO ₂ ) are advantageous in the context of the present invention as propellants (both individually as in any mixtures with each other).

Of course, the expert knows that there are other nontoxic propellants, which are basically for the realization of the present invention in the form of aerosol preparations However, because of harmful effects on the environment or other accompanying circumstances should be omitted, in particular halogenated (with fluorine, Chlorine, bromine, iodine and / or astatine substituted) hydrocarbons such as fluorocarbons and chlorofluorocarbons (CFC).

The mentioned gases can within the meaning of the present invention individually or in any desired mixtures be used to each other.

Advantageous For the purposes of the present invention, the volume fraction of propellant from the range of 0.1 to 30 vol .-%, based on the total volume from filling material and propellant gas selected (corresponding to a volume fraction of 70 to 99.9 vol .-% of contents).

Especially preferred propellant gas in the context of the present invention is carbon dioxide. Particularly advantageous are available from preparations according to the invention foams, which contain carbon dioxide as one or the active ingredient.

Especially advantageous, fine creamy and rich foams are available, when the preparations of the invention with the help of linear or branched, halogenated or non-halogenated hydrocarbons are foamed. Most notably advantageous foams are by foaming the preparations according to the invention with carbon dioxide, oxygen, compressed air, helium, krypton, xenon, Radon, argon and / or nitrogen (both individually and in any Mixtures with each other) available.

The cosmetic preparations according to the invention can contain cosmetic excipients, such as those commonly used in such preparations be used, for. Preservatives, preservatives, Complexing agents, bactericides, perfumes, preventing substances or increasing the foaming, dyes, Pigments that have a coloring Have effect, thickener, moisturizing and / or moisturizing Substances, fillers, the skin feeling improve, fats, oils, Waxes or other usual Ingredients of a cosmetic formulation such as alcohols, polyols, Polymers, foam stabilizers, electrolytes, organic solvents or silicone derivatives.

Advantageous preservatives for the purposes of the present invention are, for example, formaldehyde releasers (such as DMDM hydantoin, which is available, for example, under the trade name Glydant ^™ from Lonza), iodopropyl butylcarbamates (for example those sold under the trade names Glycacil-L, Glycacil -S. From the company. Lonza available and / or Dekaben LMB from Jan Dekker), parabens (ie p-Hydroxybenzoesäurealkylester, such as methyl, ethyl, propyl and / or Butylparaben), phenoxyethanol, ethanol, benzoic acid and the like. Usually, the preservation system according to the invention comprises fer ner also beneficial preservative, such as ethylhexylglycerol, Glycine soy etc.

advantageous Complexing agents in the sense of the present invention are, for example EDTA, [S, S] -ethylenediamine disuccinate (EDDS), which is for example available under the trade name Octaquest from the company Octel, Pentasodium ethylenediamine tetramethylene phosphonate, which z. B. available under the trade name Dequest 2046 from the company Monsanto and / or iminodisuccinic acid, which u. a. from Bayer AG under the trade name Iminodisuccinat VP OC 370 (about 30% solution) and Baypure CX 100 available is.

Especially advantageous preparations are also obtained if, as additional or agents used antioxidants. Included in the invention the preparations advantageously one or more antioxidants. As cheap, but yet optional antioxidants can all be used for cosmetic Applications suitable or common Antioxidants are used.

Especially For the purposes of the present invention, water-soluble antioxidants may be advantageous be used, such as vitamins, eg. As ascorbic acid and their derivatives.

preferred Antioxidants are also vitamin E and its derivatives as well as vitamin A and its derivatives.

The Amount of antioxidants (one or more compounds) in the Preparations is preferably from 0.001 to 30% by weight, particularly preferably from 0.05 to 20 Wt .-%, in particular 0.1 to 10 wt .-%, based on the total weight the preparation.

Provided Vitamin E and / or derivatives thereof are the antioxidant (s), is advantageous, their respective concentrations from the field from 0.001 to 10% by weight, based on the total weight of the formulation, to choose.

Provided Vitamin A or vitamin A derivatives, or carotenes or their derivatives the one or more antioxidants are advantageous, their respective Concentrations from the range of 0.001 to 10 wt .-%, based on the total weight of the formulation to choose.

It is particularly advantageous when the cosmetic preparations according to the present Contain cosmetic active ingredients, preferred agents Antioxidants are what protect the skin from oxidative stress protect can.

Further advantageous active ingredients in the context of the present invention are natural active ingredients and / or derivatives thereof, such as. Alpha-lipoic acid, phytoene, D-biotin, coenzyme Q10, alpha-glucosylrutin, carnitine, carnosine, natural and / or synthetic isoflavonoids, creatine, creatinine, taurine and / or β-alanine, and 8-hexadecene-1,16- dicarboxylic acid (dioic acid, CAS number 20701-68-2, provisional INCI name octadecenedioic acid) and / or licochalcone A, which is characterized by the following structural formula:

Licochalcon may also be used advantageously as a component of plant extracts, in particular of aqueous radix Glycyrrhizae inflatae, are used.

It is advantageous according to the invention when the cosmetic preparations 0.001 to 10 wt .-%, in particular 0.05 to 5 wt .-%, especially 0.01 to 2 wt .-% of an extract from Radix Glycyrrhizae inflatae, in each case based on the Total weight of the preparation.

All it is particularly advantageous to start from an extract which under the name Polyol Soluble Licorice Extract PU (INCI name Glycyrrhiza Inflata) can be obtained from the company Maruzen. The extract from Radix Glycyrrhizae inflatae contains about 25% % Licochalcone A.

Inventive formulations, which z. B. known anti-wrinkling agents such as flavone glycosides (especially α-glycosylrutin), Coenzyme Q10, vitamin E and / or derivatives and the like, are particularly advantageous for protection against aesthetics unattractive skin changes, as they are z. B. occur during skin aging (such as Dryness, roughness and formation of dry wrinkles, itching, reduced refatting (eg after washing), visible vascular dilations (telangiectasias, Cuperosis), slackness and development of wrinkles and wrinkles, local hyper-, hypo- and false pigmentations (eg age spots), increased susceptibility across from mechanical stress (eg cracking) and the like). Farther Advantageously, they are suitable against the appearance of dry or rough skin.

The Water phase of the preparations according to the present invention can be beneficial usual contain cosmetic excipients, such as alcohols, in particular such low C number, preferably ethanol and / or Isopropanol, diols or polyols of low C number and their ethers, preferably propylene glycol, glycerol, butylene glycol, ethylene glycol, Ethylene glycol monoethyl or monobutyl ether, propylene glycol monomethyl, monoethyl or monobutyl ether, diethylene glycol monomethyl or monoethyl ether and analogous products, polymers, foam stabilizers, Electrolytes, and in particular one or more thickeners, which or which can be chosen advantageously from the group silicon dioxide, aluminum silicates, polysaccharides or their derivatives, eg. Hyaluronic acid, Xanthan gum, hydroxypropyl methylcellulose, particularly advantageous from the group of polyacrylates, preferably a polyacrylate from the Group of so-called Carbopole [from the company. Bf. Goodrich], for example Carbopols Types 980, 981, 1382, 2984, 5984, ETD 2020, ETD 2050, Ultrez 10, either individually or in combination.

The Preparations according to the present invention Invention can furthermore advantageously also self-tanning substances such as dihydroxyacetone and / or melanin derivatives in concentrations of 1 wt .-% up to 8 wt .-%, based on the Total weight of the preparation.

Further advantageously, the compositions according to the present invention may also contain repellents for protection against mosquitoes, ticks and spiders and the like. Advantageous z. N, N-diethyl-3-methylbenzamide (trade name: meta-delphphene, "DEET"), dimethyl phthalate (trade name: Palatinol M, DMP), 1-piperidinecarboxylic acid 2- (2-hydroxyethyl) -1-methylpropyl ester, and especially 3- (Nn-butyl-N-acetyl-amino) -propionic acid ethyl ester (available under the trade name insect repellent ^® 3535 from Fa. Merck). the repellents may be used as well in combination, both separately.

When Moisturizers are substances or mixtures of substances, which give cosmetic properties the property after application or distributing on the skin surface the moisture release of the Horn layer (also called transepidermal water loss (TEWL)) to reduce and / or to positively influence the hydration of the horny layer.

Advantageous moisturizers for the purposes of the present invention are, for example, glycerol, lactic acid and / or lactates, in particular sodium lactate, butylene glycol, propylene glycol, methylpropanediol, biosaccharide gum-1, glycine soya, ethylhexyloxyglycerol, pyrrolidonecarboxylic acid and urea. Furthermore, it is particularly advantageous to use polymeric moisturizers from the group of water-soluble and / or water-swellable and / or water-gellable polysaccharides. Hyaluronic acid, chitosan and / or a fucose-rich polysaccharide, for example, which are filed in the Chemical Abstracts under the registry number 178463-23-5 and z. B. under the name Fucogel ^® 1000 of the company SOLABIA SA is available. Moisturizers can also be used advantageously as anti-wrinkle active ingredients for the protection of cosmetic skin changes, as described, for example, in US Pat. B. occur during skin aging, can be used.

The cosmetic preparations according to the invention can furthermore advantageously, although not necessarily, contain fillers which, for. B. further improve the sensory and cosmetic properties of the formulations and, for example, cause or enhance a velvety or silky feel on the skin. Advantageous fillers for the purposes of the present invention are starch and starch derivatives (such as, for example, tapioca starch, distarch phosphate, aluminum or sodium starch, octenylsuccinate and the like), pigments which have neither chiefly UV filter nor coloring action (such as, for example, US Pat. B. boron nitride etc.) and / or Aerosils ^® (CAS no. 7631-86-9).

The The following examples are intended to illustrate the present invention, without restricting it. All Quantities, percentages and percentages are, unless otherwise stated indicated on the weight and the total amount or on the total weight the preparations.

Examples

• • UVASorb^® K2A = 2,4-bis-[5-1(dimethylpropyl)benzoxazol-2-yl-(4-phenyl)-imino]-6-(2-ethylhexyl)-imino-1,3,5-triazin [CAS Nr. 288254-16-0]
• • Uvinul^® A Plus = 2-(4'-Diethylamino-2'-hydoxybenzoyl)-benzoesäurehexylester (auch: Aminobenzophenon)

In the following examples,

• • Uvasorb K2A ^® = 2,4-bis- [5-1 (dimethylpropyl) benzoxazol-2-yl- (4-phenyl) imino] -6- (2-ethylhexyl) imino-1,3,5-triazine [CAS No. 288254-16-0]
• • Uvinul ^® A Plus = 2- (4'-diethylamino-2'-hydroxybenzoyl) benzoate (also: aminobenzophenone)

Foamy O / W emulsions:

further foamy O / W emulsions:

further foamy O / W emulsions:

to Preparation of the foam are 80-97 vol .-% of the emulsion I with 3-20 Vol .-% of a suitable gas (e.g., propane / butane, compressed air, nitrogen) frothed.

Claims (8)

Foam shaped, or foamable cosmetic preparations containing 2-phenylethyl benzoate and one or more UV filter substances from the group of triazine derivatives. Use of 2-phenylethyl benzoate for foam reinforcement and Foam stabilization of self-foaming, foamy, after-foaming or foamable cosmetic preparations containing one or more UV filter substances from the group of triazine derivatives. A preparation according to claim 1 or use according to Claim 2, characterized in that the preparation one or several UV filter substances selected from the group of triazine derivatives the group of compounds 2,4-bis - {[4- (2-ethyl-hexyloxy) -2-hydroxy] -phenyl} -6- (4-methoxyphenyl) -1,3,5-triazine, Dioctylbutylamidotriazone, 2,4-bis- [5-1 (dimethylpropyl) benzoxazol-2-yl- (4-phenyl) -imino] -6- (2-ethylhexyl) -imino-1,3,5-triazine, 4,4 ', 4' '- (1,3,5-triazine-2,4,6-triyltrümino) -tris-benzoic acid tris (2-ethylhexyl) contain. Preparation or use according to one of the preceding Claims, characterized in that it contains 2-phenylethyl benzoate in a concentration from 2 to 10% by weight, based on the total weight of the preparation, contains. Preparation or use according to one of the preceding Claims, characterized in that they UV filter substances from the group the triazine derivatives in a concentration of 0.1 to 10% by weight, based on the total weight of the preparation contains. Preparation or use according to one of the preceding claims, characterized in that the preparations have a mean bubble size of 0.005 to 0.5 mm ² . Preparation or use according to one of the preceding Claims, characterized in that the preparation further UV filter substances contains. Use of 2-phenylethyl benzoate for reduction the bubble size of self-foaming, foam-like, after-foaming or foamable cosmetic preparations.