WO2008155059A2 - Hydrocarbon mixtures and use thereof - Google Patents
Hydrocarbon mixtures and use thereof Download PDFInfo
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- WO2008155059A2 WO2008155059A2 PCT/EP2008/004701 EP2008004701W WO2008155059A2 WO 2008155059 A2 WO2008155059 A2 WO 2008155059A2 EP 2008004701 W EP2008004701 W EP 2008004701W WO 2008155059 A2 WO2008155059 A2 WO 2008155059A2
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- hydrocarbons
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- linear
- hydrocarbon
- hydrocarbon mixture
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/01—Hydrocarbons
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/31—Hydrocarbons
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/04—Preparations for care of the skin for chemically tanning the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
Definitions
- the present invention relates to hydrocarbon mixtures containing 14 C isotopes, their use in cosmetic and / or pharmaceutical preparations, as well as cosmetic and / or pharmaceutical preparations containing hydrocarbon mixtures containing 14 C isotopes.
- Sensory light oil bodies are used by the cosmetic industry in a large number of formulations, in particular for decorative cosmetics or in care formulations so-called “light” components.
- These components may be, for example, volatile cyclic silicones (e.g., cyclopentasiloxane or cyclomethicone) or hydrocarbons from petrochemical processes. Because of their production, the latter substances are predominantly mixtures of linear, cyclic and branched hydrocarbons, the flashpoint of which may well be below 50 ° C. (as in the case of isododecane). Examples and application descriptions of such formulations can be found in standard works such as: Handbook of Cosmetic Science and Technology, A. Barel, M. Paye, H. Maibach, Marcel Dekker Inc. 2001. For toxicological, ecological or safety reasons, however, there will in future be a demand for alternative raw materials for such formulation tasks.
- mineral oil refers to the liquid distillation products obtained from mineral raw materials (petroleum, lignite and hard coal), which essentially consist of mixtures of saturated hydrocarbons having a linear, cyclic and / or branched structure
- mineral raw materials petroleum, lignite and hard coal
- these hydrocarbon mixtures must be extensively cleaned and chemically modified before they meet the requirements for cosmetic raw materials.
- the object of the invention was to find alternative raw materials that are ecologically and toxicologically harmless. It was of particular interest to provide raw materials which can be used directly in cosmetic or pharmaceutical preparations without expensive purification steps. Preferably, these raw materials should be available on the basis of renewable resources. These raw materials should be able to be used directly in typical cosmetic and / or pharmaceutical formulations without application restrictions.
- the raw materials should have improved sensor technology compared to the hydrocarbon mixtures of the prior art, it was also desirable that these raw materials have a better skin compatibility. It was of particular interest to provide raw materials which are comparable with respect to their formulation or sensory use possibilities with silicone oils, in particular with low-viscosity silicone oils, such as eg dimethicones. It was desirable in particular to provide raw materials which are suitable as substitutes for silicone oils. In addition, it has been of interest to provide raw materials which have an improved CO 2 balance over the prior art raw materials.
- a further object was to provide raw materials which allows a stable formulation with AP / Deo ( ⁇ antiperspirant / deodorant) agents.
- Cosmetic preparations of the antiperspirant / deodorant category in particular in so-called “stick formulations", still have the problem of insufficient stability of the cosmetic base, in which case, inter alia, the hardness of the manufactured "stick formulation” is in need of improvement.
- a disadvantage of an existing "stick formulation” is that odor changes occur during storage. [Daher say]
- a further object of the invention was therefore to provide raw materials which make it possible to use antiperspirant or deodorizing preparations, in particular those in stick formulation "stable to provide. These preparations should not show any undesirable odor developments, especially during prolonged storage.
- Another task was to provide raw materials, which give a sensory "light” impression, preferably with the same improved skin compatibility, especially in combination with UV Sunscreen filters and in conjunction with self-tanner.
- new raw materials that allow a sensory beneficial impression in decorative cosmetic formulations.
- good dispersibility of pigments is desirable.
- An object of the invention relates to a hydrocarbon mixture containing 14 C isotopes and wherein the hydrocarbon mixture contains at least 2 mutually different hydrocarbons whose carbon number differs by more than 1.
- the term "2 different hydrocarbons" refers to hydrocarbons having a different C number.
- the mixture contains at least one further hydrocarbon with a C number greater than or equal to n + 2 or less than or equal to n-2 ,
- n is an odd number, in particular 7, 9, 11, 13, 15, 17, 19, 21 and / or 23.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, wherein the hydrocarbon mixture contains at least 2 mutually different hydrocarbons whose carbon number is about 2 different.
- the hydrocarbon mixture in addition to the hydrocarbon having a C number of n nor at least one hydrocarbon having a C number of n + 2.
- the hydrocarbons in the hydrocarbon mixture differ by a maximum of 10 carbon atoms, preferably by a maximum of 8 carbon atoms, more preferably by a maximum of 6 carbon atoms, preferably by a maximum of 4 carbon atoms.
- the invention further comprises a hydrocarbon mixture containing 14 C isotopes containing a hydrocarbon having a C number of n and at least one further hydrocarbon having a C number of n + 2 and / or n + 4 and / or n + 6 and / or n + 8 and / or n + 10.
- the hydrocarbons are selected from the group of hydrocarbons having 7 to 23 carbon atoms, preferably having 11 to 21 carbon atoms.
- hydrocarbon mixture means mixtures of hydrocarbons which contain up to 10% by weight of substances which do not belong to the hydrocarbons.
- the wt .-% information of the hydrocarbons each refer to the sum of the hydrocarbons present in the mixture.
- the non-hydrocarbons present up to 10% by weight are not taken into account for this calculation.
- the substances which do not belong to the hydrocarbons and which may contain up to 10% by weight, in particular up to 8% by weight, preferably up to 5% by weight, in the hydrocarbon mixture according to the invention are, for example, fatty alcohols , which remain as unreacted starting materials in the hydrocarbon mixture.
- CX hydrocarbon includes hydrocarbons having a C number of X, for example, the term Cl 1 hydrocarbon includes all hydrocarbons having a C number of 1 1.
- total hydrocarbons includes all hydrocarbons in the mixture, regardless of their carbon number.
- isotopes also differ by angular momentum (nuclear spin), magnetic moment and electric quadrupole moment.
- the radioactive carbon isotope 14 C (8 neutrons, 6 protons) is formed from the nitrogen atom, so the mass number remains the same.
- carbon 12 C has 6 neutrons and 6 protons - so it is lighter than 14 C.
- the 14 C generated in the atmosphere combines with existing oxygen to form carbon dioxide.
- the photosynthesis of the plants then causes 14 C to enter the biosphere. Since living organisms constantly exchange carbon with the atmosphere during their metabolism, in living organisms the same distribution ratio of the 3 carbon isotopes 12 C-12, 13 C-12 and 14 C occurs as in the atmosphere: living organisms contain 10 per cent 12 stable 12 C u. 13 C isotopes ca. 1, 2 radioactive 14 C isotopes.
- Fossil fuels such as oil, natural gas or coal, were created over 100 million years ago, ie these fuels no longer contain 14 C isotopes because the original 14 C isotopes have decayed and no new 14 C isotopes have been taken up.
- hydrocarbons derived from fossil sources do not contain 14 C isotopes.
- the invention relates to hydrocarbon mixtures containing 14 C isotopes.
- the hydrocarbon mixture according to the invention contains at least two different hydrocarbons.
- the invention relates to mixtures in which at least one hydrocarbon contains 14 C isotopes, preferably contain 2 different hydrocarbons 14 C isotopes. In a preferred embodiment of the invention, all hydrocarbons present in the hydrocarbon mixture contain 14 C isotopes.
- the hydrocarbon mixture according to the invention comprises n-undecane and n-tridecane
- at least one of the hydrocarbons must contain 14 C isotopes, ie either n-undecane or n-tridecane, preferably both hydrocarbons contain 14 C isotopes.
- the proportion of the 14 C isotope is the 12 C isotope in greater than or equal 1x10 ⁇ 16, in particular at greater than or equal Ixio "15, preferably greater than or equal 7,5xlO" 14, preferably greater than or equal l, 5xl ⁇ '13 , in particular greater than or equal 3xlO "13, preferably in the range of 6xlO" 13 to l, 2xl ⁇ .
- "12 reference are all known in the hydrocarbon mixture hydrocarbons.
- the l4 C content of a sample can be determined either by counting the decaying I4 C isotopes in the counting tube (counting tube method according to Libby), in the liquid scintillation spectrometer or by counting the remaining 14 C isotopes with the accelerator mass spectrometry.
- accelerator mass spectrometry abbreviation: AMS of ⁇ ccelerator Mass Spectrometry
- 14 C isotopes can be detected with the aid of nuclear physics measuring methods in the ppt to ppq range (from 1 (T 12 to KT 16 ) in the smallest sample quantities (milligram range).
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, wherein the hydrocarbon mixture contains at least 2 mutually different hydrocarbons whose carbon number differs by more than 1 and which is less than or equal to 50 wt .-%, in particular less than or equal to 20 %
- By weight in particular less than or equal to 10% by weight, preferably less than or equal to 8% by weight, preferably less than or equal to 5% by weight, preferably less than or equal to 3% by weight, preferably less than or equal to 2% by weight, in particular less than or equal to 1 wt .-% branched hydrocarbons based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, wherein the hydrocarbon mixture contains at least 2 mutually different hydrocarbons whose carbon number differs by more than 1 and which is less than 20 wt .-%, in particular less than 10 Wt .-%, preferably less than or equal to 8 wt .-%, preferably less than or equal to 5 wt .-%, preferably less than or equal to 3 wt .-%, preferably less than or equal to 2 wt .-%, in particular less than 1 wt .-% aromatic Containing hydrocarbons based on the sum of hydrocarbons.
- the hydrocarbon mixture contains less than or equal to 0.1, in particular less than or equal to 0.01, in particular less than or equal to 0.001% by weight of aromatic hydrocarbons, based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, wherein the hydrocarbon mixture contains at least 2 mutually different hydrocarbons whose carbon number differs by more than 1 and which is less than or equal to 50 wt .-%, in particular less than or equal to 20 Wt .-%, in particular less than or equal to 10 wt .-%, preferably less than or equal to 8 wt .-%, preferably less than or equal to 5 wt .-%, preferably less than or equal to 3 wt .-%, preferably less than or equal to 2 wt .-%, in particular less than or equal to 1% by weight of unsaturated hydrocarbons, based on the sum of the hydrocarbons.
- the hydrocarbon mixture contains less than or equal to 0.1, in particular less than or equal to 0.01, in particular less than or equal to 0.001% by weight of unsaturated hydrocarbons, based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, wherein the hydrocarbon mixture is at least 2 from each other contains various hydrocarbons whose carbon number differs by more than 1 and which is less than 20 wt .-%, in particular less than or equal to 15 wt .-%, in particular less than or equal to 10 wt .-%, preferably less than or equal to 9 wt .-%, preferably less than or equal to 8% by weight, preferably less than or equal to 5% by weight, of even-numbered hydrocarbons, based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, wherein the hydrocarbon mixture contains at least 2 different hydrocarbons whose carbon number differs by more than 1 and in which the 2 mutually different hydrocarbons at least 50 wt .-%, preferably at least 60% by weight, preferably at least 70% by weight, preferably at least 80% by weight, preferably at least 90% by weight, based on the sum of the hydrocarbons.
- these hydrocarbons which are different from one another, to be hydrocarbons which differ by 2 in the C number. That in a preferred embodiment of the hydrocarbon mixture according to the invention, at least 50 wt .-%, preferably at least 60 wt .-%, preferably at least 70 wt .-%, preferably at least 80 wt .-%, preferably at least 90 wt .-% - based on the sum of the hydrocarbons, from a hydrocarbon with the C number n and a hydrocarbon with the C number n + 2.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, wherein the hydrocarbon mixture contains at least 2 mutually different hydrocarbons whose carbon number differs by more than 1 and which linear CI l and linear C 13 hydrocarbons.
- the linear C11 is hydrocarbyl n-undecane.
- the linear Cl 3 hydrocarbon is n-tridecane.
- the hydrocarbon mixture according to the invention mixture contains linear CI l and linear Cl 3 hydrocarbons and at least one further linear hydrocarbon selected from the group consisting of C12, C15, C16, C17, C18, C 19, C20, C21 and C23 hydrocarbons, preferably selected from the group consisting of C 15, C 17, C 19, C21 and C23 hydrocarbons.
- Preferred are linear, saturated hydrocarbons.
- a linear Cl 5 carbon n-pentadecane is preferred, as a linear C17 hydrocarbon n-heptadecane is preferred, as a linear C19 hydrocarbon n-nonadecane is preferred.
- the hydrocarbon mixture according to the invention contains linear C 1 l and linear C 3 hydrocarbons and at least one linear C 5 hydrocarbon and / or one linear C 7 hydrocarbon.
- a linear Cl 5 carbon n-pentadecane is preferred, as a linear C 17 hydrocarbon n-heptadecane is preferred.
- One embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, the mixture containing
- hydrocarbon mixtures containing 14 C isotopes which are particularly preferred.
- Linear C-13 hydrocarbons preferably, preferably n-tridecane based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, characterized in that the sum of the linear CI l and linear C13 hydrocarbons greater than or equal to 70 wt .-%, in particular greater than or equal to 80 wt .-%, preferably greater than or equal to 90 wt.%, Particularly preferably greater than or equal to 95 wt .-%, in particular greater than or equal to 99 wt. %, based on the sum of the hydrocarbons.
- the weight ratio of linear C 1 -hydrocarbons to linear C-13-hydrocarbons is from 1.5 to 3.5.
- hydrocarbon mixtures according to the invention in which the linear C11 and / or linear C13 hydrocarbons are saturated hydrocarbons, preferably both the linear C11 and the linear C13 hydrocarbon is a saturated hydrocarbon (n-undecane and n-tridecane).
- the hydrocarbon mixtures of the invention contain less than or equal to 10% by weight, in particular less than or equal to 5% by weight, preferably less than or equal to 3% by weight, of C 12 hydrocarbons, based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes containing linear CI l and linear Cl 3 hydrocarbons, wherein the sum of the linear C 1 and C 13 linear hydrocarbons greater than or equal to 60 wt.% Based on the sum of Hydrocarbons and wherein the sum of hydrocarbons having a C chain length greater than or equal to 14, less than or equal to 15 wt .-%, based on the sum of the hydrocarbons is.
- Hydrocarbon mixtures in which the sum of the hydrocarbons having a C chain length of less than or equal to 14, less than or equal to 10% by weight, in particular less than or equal to 8% by weight, preferably less than or equal to 4% by weight, in particular less than or equal to, are particularly preferred 2 wt .-%, in each case based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes containing linear C11 and linear C13 hydrocarbons, wherein the sum of the linear C11 and C13 linear hydrocarbons greater than or equal to 60 wt.% Based on the sum of the hydrocarbons is and the sum of Hydrocarbons having a C chain length of less than or equal to 10, less than or equal to 3% by weight, in particular less than or equal to 2% by weight, preferably less than or equal to 1.5% by weight, in particular less than or equal to 1% by weight, based on the sum of the hydrocarbons is.
- the hydrocarbon mixture according to the invention contains C12 and C14 hydrocarbons, preferably in the same weight ratio to each other as the linear C11 hydrocarbons to the linear C13 hydrocarbons.
- both the weight ratio of linear C 11 hydrocarbons to linear C 13 hydrocarbons and the weight ratio of C 12 to C 14 hydrocarbons is 1.5 to 3.5.
- a hydrocarbon mixture with linear C11 and linear C15 hydrocarbons A preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, wherein the hydrocarbon mixture contains at least 2 mutually different hydrocarbons whose carbon number differs by more than 1 and which linear Cl l and linear Cl 5 hydrocarbons.
- the linear C11 is hydrocarbyl n-undecane.
- the linear Cl 5 hydrocarbon is n-pentadecane.
- the hydrocarbon mixture according to the invention contains linear C 11 and linear C 15 hydrocarbons and at least one further linear hydrocarbon selected from the group consisting of C 12, C 13, C 14, C 16, C 17, C 18, C 19 , C20, C21 and C23 hydrocarbons, preferably selected from the group consisting of C13, C17, C19, C21 and C23 hydrocarbons.
- Preferred are linear, saturated hydrocarbons.
- a linear Cl 3 carbon n-tridecane is preferred, as a linear C17 hydrocarbon n-heptadecane is preferred, as a linear C 19 hydrocarbon n-nonadecane is preferred.
- the hydrocarbon mixture according to the invention contains linear C11 and linear C15 hydrocarbons and at least one linear C13 hydrocarbon and / or one linear C17 Hydrocarbon.
- a linear Cl 3 carbon n-tridecane is preferred, as a linear C17 hydrocarbon n-heptadecane is preferred.
- One embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, the mixture containing
- hydrocarbon mixtures containing 14 C isotopes which are particularly preferred.
- Linear C-15 hydrocarbons preferably, preferably n-pentadecane based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, characterized in that the sum of the linear CI and linear C15 hydrocarbons greater than or equal to 70 wt .-%, in particular greater than or equal to 80 wt .-%, preferably greater than or equal to 90% by weight, more preferably greater than or equal to 95% by weight, in particular greater than or equal to 99% by weight, based on the sum of the hydrocarbons.
- the weight ratio of linear C11 hydrocarbons to linear C15 hydrocarbons is 1.5 to 3.5.
- hydrocarbon mixtures according to the invention in which the linear C11 and / or linear C15 hydrocarbons are saturated hydrocarbons, preferably both the linear C11 and the linear C13 hydrocarbon is a saturated hydrocarbon (n-undecane and n-pentadecane).
- the hydrocarbon mixtures of the invention contain less than or equal to 10% by weight, in particular less than or equal to 5% by weight, preferably less than or equal to 3% by weight, of C 12 hydrocarbons based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes containing linear CI l and linear C15 hydrocarbons, wherein the sum of the linear CI l and linear C15 hydrocarbons equal to or greater than 60 wt.% Based on the sum of the hydrocarbons is and wherein the sum of the hydrocarbons having a C chain length greater than or equal to 16, less than or equal to 15 wt .-%, based on the sum of the hydrocarbons is.
- Hydrocarbon mixtures in which the sum of the hydrocarbons having a C chain length of less than or equal to 14, less than or equal to 10% by weight, in particular less than or equal to 8% by weight, preferably less than or equal to 4% by weight, in particular less than or equal to, are particularly preferred 2 wt .-%, in each case based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes containing linear CI l and linear Cl 5 hydrocarbons, wherein the sum of the linear C 1 l and linear C 15 hydrocarbons equal to or greater than 60 wt.% Based on the sum of Hydrocarbons and the sum of the hydrocarbons having a carbon chain length of less than or equal to 10, less than or equal to 3% by weight, in particular less than or equal to 2% by weight, preferably less than or equal to 1.5% by weight, in particular less than or equal to 1% by weight .-%, based on the sum of the hydrocarbons, is.
- the hydrocarbon mixture according to the invention contains C 12 and C 16 hydrocarbons, preferably in the same weight ratio to one another as the linear C 1 hydrocarbons to the linear C15 hydrocarbons.
- Hydrocarbon mixture with linear C13 and linear C15 hydrocarbons A preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, the hydrocarbon mixture containing at least 2 mutually different hydrocarbons whose carbon number differs by more than 1 and which linear C13 and contains linear C15 hydrocarbons.
- the linear Cl 3 hydrocarbon is n-tridecane.
- the linear C15 hydrocarbon is n-pentadecane.
- the hydrocarbon mixture according to the invention contains linear Cl 3 and linear C 5 hydrocarbons and at least one further linear hydrocarbon selected from the group consisting of CI 1, Cl 2, Cl 4, Cl 6, Cl 7, C 18, C 19, C20, C21 and C23 hydrocarbons, preferably selected from the group consisting of CI l, C 17, C 19, C21 and C23 hydrocarbons.
- Preferred are linear, saturated hydrocarbons.
- N-undecane is preferred as the linear C 1 l carbon
- n-heptadecane being preferred as the linear C r 7 hydrocarbon
- n-nonadecane being preferred as the linear C 19 hydrocarbon.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, the mixture containing
- hydrocarbon mixtures which contain 14 C isotopes which comprise (a) 55 to 80% by weight, in particular 60 to 75% by weight, in particular 65 to 70% by weight, of linear C-13 hydrocarbons, preferably n-tridecane (B) 20 to 45 wt .-%, in particular 24 to 40 wt .-%, in particular 24 to 30 wt.% Linear C-15 hydrocarbons, preferably, preferably n-pentadecane based on the sum of the hydrocarbons
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, characterized in that the sum of the linear C 13 and linear C 15 hydrocarbons greater than or equal to 70 wt .-%, in particular greater than or equal to 80 wt .-%, is preferred greater than or equal to 90% by weight, more preferably greater than or equal to 95% by weight, in particular greater than or equal to 99% by weight, based on the sum of the hydrocarbons.
- the weight ratio of linear C13 hydrocarbons to linear C15 hydrocarbons is 1.5 to 3.5.
- hydrocarbon mixtures according to the invention in which the linear C13 and / or linear C15 hydrocarbons are saturated hydrocarbons, preferably both the linear C13 and the linear C15 hydrocarbon is a saturated hydrocarbon (n-tridecane and n-pentadecane).
- the hydrocarbon mixtures according to the invention contain less than or equal to 10% by weight, in particular less than or equal to 5% by weight, preferably less than or equal to 3% by weight, of C 14 hydrocarbons, based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes containing linear C 13 and linear C 5 hydrocarbons, wherein the sum of the linear C 13 and linear C 15 hydrocarbons greater than or equal to 60 wt.% Based on the sum of Hydrocarbons and wherein the sum of the hydrocarbons having a C chain length greater than or equal to 16, less than or equal to 15 wt .-%, based on the sum of the hydrocarbons, is.
- hydrocarbon mixtures in which the sum of the Hydrocarbons having a C chain length greater than or equal to 16, less than or equal to 10% by weight, in particular less than or equal to 8% by weight, preferably less than or equal to 4% by weight, in particular less than or equal to 2% by weight, based in each case on Sum of hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes containing linear C13 and linear Cl 5 hydrocarbons, wherein the sum of the linear C 13 and linear C 15 hydrocarbons greater than or equal to 60 wt.% Based on the sum of Hydrocarbons and the sum of hydrocarbons having a C chain length of less than or equal to 12, less than or equal to 3 wt .-%, in particular less than or equal to 2 wt .-%, preferably less than or equal to 1.5 wt .-%, in particular less than 1 wt .-%, based on the sum of the hydrocarbons, is.
- the hydrocarbon mixtures according to the invention contain C 14 and C 16 hydrocarbons, preferably in the same weight ratio to each other as the linear C 3 hydrocarbons to the linear C15 hydrocarbons.
- both the weight ratio of linear C13 hydrocarbons to linear C15 hydrocarbons and the weight ratio of C14 to C16 hydrocarbons is from 1.5 to 3.5.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, wherein the hydrocarbon mixture contains at least 2 mutually different hydrocarbons whose carbon number differs by more than 1 and which linear C15 and linear Cl 7 hydrocarbons.
- the linear Cl 5 hydrocarbon is n-pentadecane.
- the linear Cl 7 hydrocarbon is n-heptadecane.
- the hydrocarbon mixture according to the invention comprises linear C15 and linear C17 hydrocarbons and at least one further linear hydrocarbon selected from the group consisting of CI1, C12, C13, C14, C16, C18, C19, C20, C21 and C23 hydrocarbons, preferably selected from the Group consisting of CI l, C 13, C 19, C21 and C23 hydrocarbons.
- Preferred are linear, saturated hydrocarbons.
- N-undecane is preferred as the linear C 1 carbon
- n-tridecane being preferred as the linear C 13 hydrocarbon
- n-nonadecane being preferred as the linear C 19 hydrocarbon.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, the mixture containing
- Pentadecane (h) 10 to 50% by weight of linear C-17 hydrocarbons, preferably n-
- Heptadecane based on the sum of the hydrocarbons.
- hydrocarbon mixtures containing 14 C isotopes which are particularly preferred.
- Linear C-17 hydrocarbons preferably, preferably n-heptadecane. based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, characterized in that the sum of the linear C 15 and linear C 17 hydrocarbons greater than or equal to 70 wt .-%, in particular greater than or equal to 80 wt .-%, preferably greater than or equal to 90% by weight, more preferably greater than or equal to 95% by weight, in particular greater than or equal to 99% by weight, based on the sum of the hydrocarbons.
- the weight ratio of linear C15 hydrocarbons to linear C17 hydrocarbons is 1.5 to 3.5.
- the hydrocarbon mixtures of the invention contain less than or equal to 10% by weight, in particular less than or equal to 5% by weight, preferably less than or equal to 3% by weight, of C 16 hydrocarbons based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixtures containing 14 C isotopes containing linear C15 and linear C17 hydrocarbons, wherein the sum of the linear C 15 and linear C 17 hydrocarbons equal to or greater than 60 wt.% Based on the sum of the hydrocarbons and wherein the sum of the hydrocarbons having a C chain length greater than or equal to 18, less than or equal to 15 wt .-%, based on the sum of the hydrocarbons, is.
- Hydrocarbon mixtures in which the sum of the hydrocarbons having a C chain length greater than or equal to 18, less than or equal to 10% by weight, in particular less than or equal to 8% by weight, preferably less than or equal to 4% by weight, in particular less than or equal to, are particularly preferred 2 wt .-%, in each case based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes containing linear C15 and linear Cl 7 hydrocarbons, wherein the sum of the linear C 15 and linear C 17 hydrocarbons equal to or greater than 60 wt.% Based on the sum of Hydrocarbons and the sum of the hydrocarbons having a C chain length of less than or equal to 14, less than or equal to 3% by weight, in particular less than or equal to 2% by weight, preferably less than or equal to 1.5% by weight, in particular less than or equal to 1% by weight .-%, based on the sum of the hydrocarbons, is.
- the hydrocarbon mixtures according to the invention contain C 16 and C 18 hydrocarbons, preferably in the same weight ratio to each other as the linear C 15 hydrocarbons to the linear C 7 hydrocarbons.
- both the weight ratio of linear C15 hydrocarbons to linear C17 hydrocarbons and the weight ratio of Cl6 to Cl8 hydrocarbons is 1.5 to 3.5.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, wherein the hydrocarbon mixture contains at least 2 mutually different hydrocarbons whose carbon number differs by more than 1 and which linear Cl Contains 7 and linear C19 hydrocarbons.
- the linear C17 hydrocarbon is n-heptadecane.
- the linear C19 hydrocarbon is n-nonadecane.
- the hydrocarbon mixture according to the invention comprises linear C17 and linear C19 hydrocarbons and at least one further linear hydrocarbon selected from the group consisting of CI1, Cl2, Cl3, Cl4, Cl5, C16, C18, C20, C21 and C23 hydrocarbons, preferably selected from the group consisting of CI l, C13, C15, C21 and C23 hydrocarbons.
- Preferred are linear, saturated hydrocarbons.
- N-undecane is preferred as the linear C 1 carbon
- n-tridecane being preferred as the linear C 13 hydrocarbon
- n-nonadecane being preferred as the linear C 19 hydrocarbon.
- Particularly preferred as another linear hydrocarbon is n-henicosan (C21 linear, saturated).
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, the mixture containing
- hydrocarbon mixtures containing 14 C isotopes which are particularly preferred.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, characterized in that the sum of the linear C 17 and linear C 19 hydrocarbons greater than or equal to 70 wt .-%, in particular greater than or equal to 80 wt .-%, preferably greater than or equal to 90% by weight, more preferably greater than or equal to 95% by weight, in particular greater than or equal to 99% by weight, based on the sum of the hydrocarbons.
- the weight ratio of linear C 17 hydrocarbons to linear C 19 hydrocarbons is 1.5 to 3.5.
- hydrocarbon mixtures according to the invention in which the linear Cl 7 and / or linear C 19 hydrocarbons are saturated hydrocarbons, preferably both the linear C 17 and the linear C 19 hydrocarbon is a saturated hydrocarbon (n-heptadecane and n-nonadecane).
- the hydrocarbon mixtures according to the invention contain less than or equal to 10% by weight, in particular less than or equal to 5% by weight, preferably less than or equal to 3% by weight, of C 18 hydrocarbons, based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes containing linear C17 and linear C19 hydrocarbons, where the sum of the linear C 17 and linear C 19 hydrocarbons is greater than or equal to 60% by weight, based on the sum of the hydrocarbons, and where the sum of the hydrocarbons having a C chain length greater than or equal to 20, less than or equal to 15% by weight, based on the sum of the hydrocarbons.
- Hydrocarbon mixtures in which the sum of the hydrocarbons having a C chain length greater than or equal to 18, less than or equal to 10% by weight, in particular less than or equal to 8% by weight, preferably less than or equal to 4% by weight, in particular less than or equal to, are particularly preferred 2 wt .-%, in each case based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes containing linear Cl 7 and linear C 19 hydrocarbons, wherein the sum of linear C 17 and linear C 19 hydrocarbons greater than or equal to 60 wt.% Based on the sum of Hydrocarbons and the sum of the hydrocarbons having a C chain length of less than or equal to 16, less than or equal to 3% by weight, in particular less than or equal to 2% by weight, preferably less than or equal to 1.5% by weight, in particular less than or equal to 1% by weight .-%, based on the sum of the hydrocarbons, is.
- the hydrocarbon mixtures of the invention Cl 8 and C 20 hydrocarbons, preferably in the same weight ratio to each other as the linear Cl 7 hydrocarbons to the linear C 19 hydrocarbons.
- both the weight ratio of linear C 17 hydrocarbons to linear C 19 hydrocarbons and the weight ratio of C 18 to C 20 hydrocarbons is 1.5 to 3.5.
- Hydrocarbon mixture with linear C19 and linear C21 hydrocarbons A preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, wherein the hydrocarbon mixture contains at least 2 mutually different hydrocarbons whose carbon number differs by more than 1 and which linear C19 and contains linear C21 hydrocarbons.
- the linear C19 hydrocarbon is n-nonadecane.
- the linear C21 hydrocarbon n-henicosan.
- the hydrocarbon mixture according to the invention comprises linear C 19 and linear C 21 hydrocarbons and at least one further linear hydrocarbon selected from the group consisting of CI 1, C 12, C 13, C 14, C 15, C 16, C 17, C 18, C 20 and C 23 hydrocarbons, preferably selected from the group consisting of CI l, Cl 3, Cl 5, C17 and C 23 hydrocarbons.
- Preferred are linear, saturated hydrocarbons.
- N-undecane is preferred as the linear C 1 carbon
- n-tridecane being preferred as the linear C 13 hydrocarbon
- n-heptadecane being preferred as the linear C 7 hydrocarbon.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, the mixture containing
- hydrocarbon mixtures containing 14 C isotopes which are particularly preferred.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes, characterized in that the sum of the linear C 19 and linear C21 hydrocarbons greater than or equal to 70 wt .-%, in particular greater than or equal to 80 wt .-%, preferably greater than or equal to 90% by weight, more preferably greater than or equal to 95% by weight, in particular greater than or equal to 99% by weight, based on the sum of the hydrocarbons.
- the weight ratio of linear C19 hydrocarbons to linear C21 hydrocarbons is 1.5 to 3.5.
- hydrocarbon mixtures according to the invention in which the linear C19 and / or linear C21 hydrocarbons are saturated hydrocarbons, preferably both the linear C19 and the linear C21 hydrocarbon is a saturated hydrocarbon (n-nonadecane and n-henicosan).
- the hydrocarbon mixtures according to the invention contain less than or equal to 10% by weight, in particular less than or equal to 5% by weight, preferably less than or equal to 3% by weight, of C 20 hydrocarbons, based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes containing linear C19 and linear C21 hydrocarbons, wherein the sum of the linear C19 and C21 linear hydrocarbons greater than or equal to 60 wt.% Based on the sum of the hydrocarbons and wherein the sum of the hydrocarbons having a C chain length greater than or equal to 22, less than or equal to 15 wt .-%, based on the sum of the hydrocarbons, is.
- Hydrocarbon mixtures in which the sum of the hydrocarbons having a C chain length greater than or equal to 22, less than or equal to 10% by weight, in particular less than or equal to 8% by weight, preferably less than or equal to 4% by weight, in particular less than or equal to, are particularly preferred 2 wt .-%, in each case based on the sum of the hydrocarbons.
- a preferred embodiment of the invention relates to a hydrocarbon mixture containing 14 C isotopes containing linear C19 and linear C21 hydrocarbons, wherein the sum of the linear C19 and C21 linear hydrocarbons greater than or equal to 60 wt.% Based on the sum of the hydrocarbons and the sum of the hydrocarbons having a C chain length of less than or equal to 18, less than or equal to 3% by weight, in particular less than or equal to 2% by weight, preferably less than or equal to 1.5% by weight, in particular less than or equal to 1% by weight, based on the sum of the hydrocarbons.
- the hydrocarbon mixtures C20 and C22 according to the invention contain hydrocarbons, preferably in the same weight ratio to each other as the linear C19 hydrocarbons to the linear C21 hydrocarbons.
- both the weight ratio of linear C 19 hydrocarbons to linear C21 hydrocarbons and the weight ratio of C20 to C22 hydrocarbons is 1.5 to 3.5.
- hydrocarbon mixtures according to the invention are particularly suitable for use in cosmetic and / or pharmaceutical preparations, in particular as oil bodies and / or as dispersants.
- Another object of the invention relates to a process for the preparation of a cosmetic and / or pharmaceutical preparation, wherein a hydrocarbon mixture according to any one of claims 1 to 13 is added to a cosmetically and / or pharmaceutically suitable carrier.
- hydrocarbon mixtures according to the invention are particularly suitable for use in cosmetic preparations for the care of skin and / or hair.
- hydrocarbon mixtures according to the invention are particularly suitable for use in cosmetic preparations for sun protection.
- the hydrocarbon mixtures according to the invention are particularly suitable for use in preparations of decorative cosmetics, such as lipsticks, lip gloss, eye shadows, mascara (mascara), eye pencils (kohl), nail polish and in make-up formulations of all kinds (powder, cream, foundation, Cover pins, etc.).
- decorative cosmetics such as lipsticks, lip gloss, eye shadows, mascara (mascara), eye pencils (kohl), nail polish and in make-up formulations of all kinds (powder, cream, foundation, Cover pins, etc.
- the hydrocarbon mixtures according to the invention are particularly suitable for use in preparations for cleansing the skin and / or hair, such as shampoos, shower gels, bath additives, conditioners, etc.
- the hydrocarbon mixtures according to the invention are furthermore suitable for the preparation of finely divided emulsions, e.g. Nanoemulsions, microemulsions or PIT emulsions.
- the oil droplets are usually in the range of 10 to 1000 nm, preferably 100 to 500 nm in diameter.
- PIT emulsions for example in perfumery and cosmetics, Volume 77, No. 4/96, pp. 250-254 by Wadle et al. described.
- the hydrocarbon mixtures according to the invention can be obtained, for example, by reductive demethylation of vegetable fatty alcohols.
- the process of reductive dehydroxymethylation described in the international application PCT / EP2006 / 011647 (Cognis) is particularly suitable for the preparation of the hydrocarbon mixtures according to the invention starting from fatty alcohols of vegetable origin.
- fatty alcohols of desired C chain length can be subjected to the process described individually and the resulting hydrocarbons are mixed to give the hydrocarbon mixtures according to the invention.
- Another object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.%, Preferably 5 to 50 wt .-%, in particular 10 to 30 wt .-% of a hydrocarbon mixture containing 14 C isotopes contains.
- the wt .-% refer to the total weight of the cosmetic and / or pharmaceutical preparation.
- hydrocarbon mixtures present in the preparations according to the invention are always mixtures of at least two different hydrocarbons. These may differ in their C number by 1, 2, 3, 4 etc. carbon atoms.
- the cosmetic and / or pharmaceutical preparations contain hydrocarbons whose carbon number differs by more than 1, preferably by 2.
- the proportion of the 14 C isotope of the 12 C isotope in which contained in the inventive preparations hydrocarbon mixture is preferably greater than equal to 1 x 10 "16, in particular greater than or equal 1 x 10 ⁇ 15, preferably greater than equal to 7.5 x 10" 14, preferably not less than 1.5 x 10 "1, in particular greater than or equal to 3 x 10" ', preferably, the proportion of the 14 C isotope to the' C isotopes in the range of 6 x 10 "13 to 1.2 x 10 ⁇ 12th Reference quantity here are all hydrocarbons contained in the preparation according to the invention.
- the hydrocarbon mixture containing in the preparation according to the invention contains at least one hydrocarbon which contains 14 C isotopes, preferably contain 2 different hydrocarbons 14 C isotopes.
- the 2 different hydrocarbons whose carbon number differs by more than 1, preferably by 2, particularly preferably contain 14 C isotopes.
- the cosmetic and / or pharmaceutical preparations comprise the hydrocarbon mixtures according to one of claims 1 to 13.
- the cosmetic and / or pharmaceutical preparations according to the invention contain hydrocarbons which are selected from the group of hydrocarbons having 7 to 23 carbon atoms, preferably 11 to 21 carbon atoms.
- the cosmetic and / or pharmaceutical preparations according to the invention contain hydrocarbon mixtures which are less than or equal to 50% by weight, in particular less than or equal to 20% by weight, less than or equal to 10% by weight, preferably less than or equal to 5% by weight. in particular less than or equal to 1% by weight of branched hydrocarbons, based on the sum of the hydrocarbons
- the reference "sum of hydrocarbons" in cosmetic and / or pharmaceutical preparations includes all hydrocarbons contained in the cosmetic and / or pharmaceutical preparation, regardless of their carbon number.
- the cosmetic and / or pharmaceutical preparations according to the invention comprise hydrocarbon mixtures which are less than or equal to 20% by weight, in particular less than or equal to 10% by weight, in particular less than or equal to 5% by weight, preferably less than or equal to 1% by weight. %, aromatic hydrocarbons based on the sum of the hydrocarbons.
- the preparations contain less than or equal to 0.1, in particular less than or equal to 0.01% by weight, in particular less than or equal to 0.001% by weight, of aromatic hydrocarbons, based on the sum of the hydrocarbons.
- the cosmetic and / or pharmaceutical preparations according to the invention comprise hydrocarbon mixtures which are less than or equal to 50% by weight, in particular less than or equal to 20% by weight, less than or equal to 10% by weight, in particular less than or equal to 5% by weight. , preferably less than or equal to 1% by weight, of unsaturated hydrocarbons, based on the sum of the hydrocarbons.
- the preparations contain less than or equal to 0.1, in particular less than or equal to 0.01% by weight, in particular less than or equal to 0.001% by weight of unsaturated hydrocarbons, based on the sum of the hydrocarbons
- the cosmetic and / or pharmaceutical preparations according to the invention contain hydrocarbon mixtures which are less than or equal to 20% by weight, in particular less than or equal to 15% by weight, in particular less than or equal to 10% by weight, preferably less than or equal to 9% by weight. , in particular less than or equal to 8% by weight in particular less than or equal to 5% by weight of even-numbered hydrocarbons, based on the sum of the hydrocarbons.
- Another object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt .-%, preferably 5 to 50 wt .-%, in particular 10 to 30 wt .-% of a hydrocarbon mixture containing 14 C isotopes , and in which 2 hydrocarbons different from each other make up at least 50% by weight, preferably at least 60% by weight, based on the sum of the hydrocarbons.
- cosmetic and / or pharmaceutical preparations according to the invention in which the sum of the two mutually different hydrocarbons greater than or equal to 70 wt .-%, in particular greater than or equal to 80 wt .-%, preferably greater than or equal to 90 wt.%, Particularly preferably greater than or equal to 95 Wt .-%, in particular greater than or equal to 99 wt .-%, based on the sum of the hydrocarbons, is.
- the hydrocarbon mixture of the cosmetic and / or pharmaceutical preparation consists exclusively of 2 mutually different hydrocarbons.
- the cosmetic and / or pharmaceutical preparations according to the invention comprise from 0.1 to 80% by weight, preferably from 5 to 50% by weight, in particular from 10 to 30% by weight, of a hydrocarbon mixture which contains 14 C isotopes.
- a hydrocarbon mixture which contains 14 C isotopes.
- 2 different hydrocarbon are selected from the group consisting of linear C 11 and linear C 13 hydrocarbons, linear Cl l and linear Cl 5 hydrocarbons linear C13 and linear Cl 5 hydrocarbons, linear C 15 and linear C 17 hydrocarbons, linear C 17 and linear C 19 hydrocarbons and / or linear C 19 and linear C21 hydrocarbons.
- These preparations can be obtained, for example, by using a hydrocarbon mixture according to the invention or by using defined amounts of individual hydrocarbons.
- cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes and wherein the hydrocarbon mixture
- n represents an integer from 7 to 23, preferably 11 to 21.
- cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes, wherein the hydrocarbon mixture
- Wt.% Of a hydrocarbon having the C number n contains - 20 to 45 wt .-%, in particular 24 to 40 wt .-%, in particular 24 to 30
- Wt.% Of a hydrocarbon having the C number n contains based on the sum of the hydrocarbons, wherein n represents an integer from 7 to 23, preferably 11 to 21.
- the weight ratio of the hydrocarbons having the C number n to the hydrocarbon having the C number n + 2 in the cosmetic and / or pharmaceutical preparations is from 1.5 to 3.5.
- the cosmetic and / or pharmaceutical preparations according to the invention are light and stable cosmetic and / or pharmaceutical preparations, this is especially the case if they also contain antiperspirant / deodorant active ingredients.
- An object of the invention therefore relates to cosmetic and / or pharmaceutical Preparations containing 0.1 to 80 wt .-% of a hydrocarbon mixture containing 14 C isotopes, and at least one antiperspirant / deodorant active ingredient.
- Suitable antiperspirant / deodorant active compounds are in particular compounds selected from the group consisting of antiperspirants, esterase inhibitors, bactericidal or bacteriostatic agents and / or sweat-absorbing substances.
- Antiperspirants are salts of aluminum, zirconium or zinc.
- suitable antiperspirant active ingredients are e.g. Aluminum chloride, aluminum chlorohydrate, aluminum dichlorohydrate, aluminum sesquichlorohydrate and their complex compounds e.g. With propylene glycol-1,2.
- Aluminiumhydroxyallantoinat aluminum chloride tartrate, aluminum zirconium trichlorohydrate, aluminum zirconium tetrachlorohydrate, aluminum zirconium pen tachlorohydrat and their complex compounds z.
- amino acids such as glycine.
- aluminum chlorohydrate, aluminum zirconium tetrachlorohydrate, aluminum zirconium pentachlorohydrate and their complex compounds are used.
- the preparations according to the invention may contain the antiperspirants in amounts of from 1 to 50, preferably from 5 to 30, and in particular from 8 to 25,% by weight, based on the total weight of the cosmetic and / or pharmaceutical preparation.
- esterase inhibitors are preferably trialkyl citrates such as trimethyl citrate, tripropyl citrate, triisopropyl citrate, tributyl citrate and in particular triethyl citrate (Hydagen® CAT, Cognis GmbH, Dusseldorf / FRG).
- the substances inhibit the enzyme activity and thereby reduce odors.
- esterase inhibitors include sterol sulfates or phosphates, such as, for example, lanosterol, cholesterol, campesterol, stigmasterol and sitosterol sulfate or phosphate, dicarboxylic acids and their esters, for example glutaric acid, glutaric acid monoethyl ester, glutaric acid diethyl ester, adipic acid, Adipic acid monoethyl ester, diethyl adipate, malonic acid and diethyl malonate, hydroxycarboxylic acids and their esters such as citric acid, malic acid, tartaric acid or diethyl tartrate and zinc glycinate.
- sterol sulfates or phosphates such as, for example, lanosterol, cholesterol, campesterol, stigmasterol and sitosterol sulfate or phosphate
- dicarboxylic acids and their esters for example glutaric acid, glutaric acid monoethyl este
- the preparations according to the invention may contain the esterase inhibitors in amounts of from 0.01 to 20, preferably from 0.1 to 10, and in particular from 0.3 to 5,% by weight, based on the total weight of the cosmetic and / or pharmaceutical preparation.
- bactericidal or bacteriostatic agents are in particular chitosan and phenoxyethanol.
- 5-Chloro-2- (2,4-dichlorophenoxy) -phenol which is marketed under the trade name Irgasan® by Ciba-Geigy, Basel / CH, has also proved to be particularly effective.
- germ-inhibiting agents are basically all effective against Gram-positive bacteria substances such.
- the preparations according to the invention may contain the bactericidal or bacteriostatic agents in amounts of from 0.01 to 5 and preferably from 0.1 to 2% by weight, based on the total weight of the cosmetic and / or pharmaceutical preparation.
- modified starch such as e.g. Dry FIo Plus (National Starch), silicates, talc and other substances of similar modification that appear to be suitable for sweat absorption.
- the preparations according to the invention may contain the sweat-absorbing substances in amounts of from 0.1 to 30, preferably from 1 to 20, and in particular from 2 to 8,% by weight, based on the total weight of the cosmetic and / or pharmaceutical preparation.
- the cosmetic and / or pharmaceutical preparations according to the invention are light and stable cosmetic and / or pharmaceutical preparations, this is especially the case if they further contain at least one UV light protection filter.
- An object of the invention therefore relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes, and at least at least one UV photoprotective filter.
- An object of the invention preferably relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes and wherein the hydrocarbons contain at least 2 mutually different hydrocarbons whose carbon number exceeds by more than 1 , preferably different by 2, and at least one UV photoprotective filter.
- Erf ⁇ ndungshiel are suitable as UV light protection filter at room temperature liquid or crystalline organic substances (sunscreen), which are able to absorb ultraviolet rays and the absorbed energy in the form of longer-wave radiation, eg heat to give back.
- UV filters can be oil-soluble or water-soluble.
- Typical oil-soluble UV-B filters or broad-spectrum UV A / B filters are, for example: > 3-Benzylidencampher or 3-Benzylidennorcampher (Mexoryl SDS 20) and its derivatives, eg 3- (4-methylbenzylidene) camphor as described in EP 0693471 Bl
- Esters of cinnamic acid preferably 4-methoxycinnamic acid 2-ethylhexyl ester, 4-methoxycinnamic acid propyl ester, 4-methoxycinnamic acid isoamyl ester, 2-cyano-3,3-phenylcinnamic acid 2-ethylhexyl ester (octocrylene);
- Esters of salicylic acid preferably 2-ethylhexyl salicylate, 4-isopropyl salicylate, homomenthyl salicylate;
- benzophenone preferably 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4'-methylbenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone;
- Esters of benzalmalonic acid preferably di-2-ethylhexyl 4-methoxybenzmalonate
- Triazine derivatives e.g. 2,4,6-Trianilino- (p-carbo-2'-ethyl-r-hexyloxy) -l, 3,5-triazine and 2,4,6-tris [p- (2-ethylhexyl-oxycarbonyl) Anilino] -l, 3,5-triazine (Uvinul T 150) as described in EP 0818450 Al or 4,4 '- [(6- [4- ((1,1-dimethylethyl) amino carbonyl) phenylamino ] -l, 3,5-triazine-2,4-diyl) diimino] bis (benzoic acid 2-ethylhexyl ester) (Uvasorb® HEB);
- Propane-1,3-diones such as e.g. 1- (4-tert-butylphenyl) -3- (4'-methoxyphenyl) propane-1,3-dione;
- Suitable water-soluble UV filters are:
- Sulfonic acid derivatives of benzophenones preferably 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid and its salts;
- Sulfonic acid derivatives of the 3-benzylidene camphor e.g. 4- (2-oxo-3-bionylidenemethyl) benzenesulfonic acid and 2-methyl-5- (2-oxo-3-bomylidene) -sulfonic acid and its salts.
- UV-A filter in particular derivatives of benzoylmethane come into question, such as l- (4'-tert-butylphenyl) -3- (4'-methoxyphenyl) propane-l, 3-dione, 4-tert-butyl 4'-methoxydibenzoylmethane (Parsol® 1789), 1-phenyl-3- (4'-isopropylphenyl) propane-1,3-dione and also enamine compounds as described in DE 19712033 A1 (BASF) and benzoic acid, 2- [ 4- (diethylamino) -2-hydroxybenzoyl], hexyl ester (Uvinul® A plus).
- benzoylmethane such as l- (4'-tert-butylphenyl) -3- (4'-methoxyphenyl) propane-l, 3-dione, 4-tert-butyl 4'-methoxydibenzoylmethane (Parsol® 1789), 1-
- UV-A and UV-B filters can also be used in mixtures.
- Particularly favorable combinations consist of the derivatives of benzoylmethane, for example 4-tert-butyl-4'-methoxydibenzoylmethane (Parsol® 1789) and 2-cyano-3,3-phenylcinnamic acid 2-ethylhexyl ester (octocrylene) in combination with esters cinnamic acid, preferably 4-methoxycinnamic acid 2-ethylhexyl ester and / or 4-methoxycinnamic acid propyl ester and / or 4-methoxycinnamic acid isoamyl ester.
- benzoylmethane for example 4-tert-butyl-4'-methoxydibenzoylmethane (Parsol® 1789) and 2-cyano-3,3-phenylcinnamic acid 2-ethylhexyl ester (octocry
- water-soluble filters such as 2- Phenylbenzimidazole-5-sulfonic acid and their alkali, alkaline earth, ammonium, alkylammonium, alkanolammonium and glucammonium combined.
- UV light protection filters are those according to Annex VII of the Commission Directive (in the version of Commission Directive 2005/9 / EC of 28 January 2005 amending Council Directive 76/768 / EEC, concerning cosmetic purposes, for the purposes of adapting Annexes VII thereof to technical progress) substances, which are explicitly referred to here.
- insoluble photoprotective pigments namely finely dispersed metal oxides or salts
- suitable metal oxides are in particular zinc oxide and titanium dioxide and, in addition, oxides of iron, zirconium, silicon, manganese, aluminum and cerium and mixtures thereof.
- salts silicates (talc), barium sulfate or zinc stearate can be used.
- the oxides and salts are used in the form of the pigments for skin-care and skin-protecting emulsions and also for decorative cosmetics.
- the particles should have an average diameter of less than 100 nm, preferably between 5 and 50 nm and in particular between 15 and 30 nm.
- the pigments may have a spherical shape, but it is also possible to use those particles which have an ellipsoidal or otherwise deviating shape from the spherical shape.
- the pigments may also be surface-treated, ie hydrophilized or hydrophobicized.
- Typical examples are coated titanium dioxides, such as titanium dioxide T 805 (Degussa) or Eusolex® T, Eusolex® T-2000, Eusolex® T-Aqua, Eusolex® AVO, Eusolex® T-ECO, Eusolex® T-OLEO and Eusolex® TS (Merck).
- Typical examples are zinc oxides such as Zinc Oxide neutral, Zinc Oxide NDM (Symrise) or Z-Cote® (BASF) or SUNZnO-AS and SUNZnO-NAS (Sunjun Chemical Co. Ltd.).
- Suitable hydrophobic coating agents are in particular silicones and in particular trialkoxyoctylsilanes or simethicones.
- sunscreens so-called micro- or nanopigments are preferably used.
- micronized zinc oxide is used.
- Further suitable UV photoprotective filters are the review by P.Finkel in S ⁇ FW Journal 122, 8/1996, pp 543-548 and Parf.Kosm. Volume 80, No. 3/1999, pp. 10 to 16.
- secondary light stabilizers of the antioxidant type which interrupt the photochemical reaction chain which is triggered when UV radiation penetrates into the skin.
- Typical examples are amino acids (eg glycine, histidine, tyrosine, tryptophan) and their derivatives, imidazoles (eg urocaninic acid) and their derivatives, peptides such as D, L-carnosine, D-carnosine, L-carnosine and their derivatives (eg anserine) , Carotenoids, carotenes (eg carotene, carotene, lycopene) and their derivatives, chlorogenic acid and its derivatives, lipoic acid and its derivatives (eg dihydrolipoic acid), aurothioglucose, propylthiouracil and other thiols (eg thioredoxin, glutathione, cysteine, cystine, Cystamine and its glyco
- amino acids eg glycine, histidine, ty
- An object of the invention therefore relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes, and at least at least one UV photoprotective filter selected from the group consisting of 4-methylbenzylidene Camphor, Benzophenone-3, Butyl Methoxydibenzoylmethane, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazines, Methylene Bis-Benzotriazolyl Tetramethylbutylphenol, Diethylhexyl Butamido Triazone, Ethylhexyl Triazone and Diethylamino Hydroxybenzoyl Hexyl Benzoate, 3- (4'-Trimethylammonium) benzylidenebornan-2-one methylsulfate, 3 , 3 '- (l, 4-
- An object of the invention therefore relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes and wherein the hydrocarbons contain at least 2 mutually different hydrocarbons whose carbon number is more than 1 , preferably differing by 2, and at least one UV photoprotective filter selected from the group consisting of 4-methylbenzylidene camphor, benzophenone-3, butyl methoxydibenzoylmethane, bis-ethylhexyloxyphenol methoxyphenyl triazines, methylene bis-benzotriazolyl tetramethylbutylphenol, diethylhexyl butamido triazone, ethylhexyl triazone and diethylamino Hydroxybenzoyl hexyl benzoates, 3- (4'-trimethylammonium) benzylidenebornan-2-one methylsulfate, 3,3 '- (l,
- NeoHeliopan®MBC (INCI: 4-methylbenzylidene camphor; manufacturer: Symrise); NeoHeliopan® BB (INCI: Benzophenone-3, manufacturer: Symrise); Parsol® 1789 (INCI: Butyl Methoxydibenzoylmethane, Manufacturer: Hoffinann-La Roche (Givaudan); Tinosorb® S (INCI: Bis-Ethylhexyloxyphenol Methoxyphenyl Triazines); Tinosorb® M (INCI: Methylene Bis-Benzotriazolyl Tetramethylbutylphenol): Manufacturer: Ciba Specialty Chemicals
- Uvasorb® HEB (INCI: diethylhexyl butamido triazone, manufacturer: 3 V Inc.), Uvinul® T 150 (INCI: ethylhexyl triazone, manufacturer: BASF AG), Uvinul® A plus (INCI: diethylamino hydroxybenzoyl hex
- the preparations according to the invention may contain the UV light protection filters in amounts of from 0.5 to 30% by weight, preferably 2.5 to 20% by weight, particularly preferably 5 to 15% by weight, based on the total weight of the cosmetic and / or or pharmaceutical preparation.
- An object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 'C isotopes, and at least at least one self-tanner.
- a preferred object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes and wherein the hydrocarbons contain at least 2 mutually different hydrocarbons, the carbon number of more than 1 , preferably different by 2, and at least one self-tanner.
- Suitable active ingredients for self-tanning agents are natural or synthetic ketols or aldols. Examples of suitable active compounds are dihydroxyacetone, erythrulose, glycerol aldehyde, alloxan, hydroxymethylglyoxal, gamma-dialdehyde, 6-aldo-D-fructose, ninhydrin and meso-tartaric dialdehyde.
- Suitable self-tanning agents are, in particular, dihydroxyacetone and / or erythrulose.
- compositions according to the invention usually contain the self-tanning agents in concentrations of from 1 to 10, in particular from 2 to 5,% by weight, based on the total weight of the cosmetic and / or pharmaceutical preparation.
- An object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes, and at least at least one self-tanner and at least one UV sunscreen.
- a preferred subject of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes and wherein the hydrocarbons contain at least 2 mutually different hydrocarbons whose carbon number to more than 1, preferably differs by 2, and at least one UV photoprotective filter and at least one self-tanner.
- the cosmetic and / or pharmaceutical preparations according to the invention can be present, for example, as O / W or W / O care emulsions, sunscreen formulation, AP / Deo concepts, formulations for decorative cosmetics, oily care preparations, impregnating liquids for substrates such as paper and non-woven products. Examples include wet wipes, handkerchiefs, diapers or hygiene products.
- hydrocarbon mixtures according to the invention and the cosmetic and / or pharmaceutical preparations according to the invention are also particularly suitable for light, sprayable applications and / or as constituents of care emulsions for tissues, papers, wipes, sponges (eg polyurethane sponges), patches in the field of baby hygiene, Baby Care, Skin Care, Sunscreen, After-SunTreatment, Insect Repellent, Cleansing, Facial Cleansing, and AP / Deo application.
- the hydrocarbon mixtures according to the invention are particularly suitable as constituents of preparations of decorative cosmetics, such as lipsticks, eye make-up, such as eyeshadow, mascara, eyeliner, kohl, nail polish, etc., and make-up formulations.
- An object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes, and at least at least one pigment and / or a dye.
- a preferred subject of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 4 C isotopes and wherein the hydrocarbons contain at least 2 mutually different hydrocarbons whose carbon number is more than 1 , preferably different by 2, and at least one pigment and / or one dye.
- pigment includes particles of any shape which are white or colored, organic or inorganic, insoluble in the formulations, and serve the purpose of coloring the preparation.
- inorganic pigments are used, metal oxides are particularly preferred.
- inorganic pigments examples include: titanium dioxide, optionally surface-coated, zirconium or cerium oxides and zinc, iron (black, yellow or red) and chromium oxides, manganese violet, ultramarine blue, chromate and iron (III) blue, metal powder such as aluminum powder or copper powder.
- the pigment is selected from the inorganic pigments, preferably from the metal oxides.
- the pigment is selected from the group consisting of titanium dioxide, zinc oxide, iron oxide and mixtures thereof.
- the pigments can be present both individually and in mixtures. Pigment mixtures of white pigments (for example kaolin, titanium dioxide or zinc oxide) and inorganic color pigments (for example iron oxide pigments, chromium oxides) are preferred for the purposes of the present invention, the pigments being coated ("coated"). or uncoated. Among the color pigments, iron oxides are particularly preferred.
- the pigment or pigments can also be selected from the group of effect pigments, which of the cosmetic preparation in addition to the pure color an additional property - such.
- effect pigments are advantageously used in addition to one or more white and / or color pigments.
- the most important group of effect pigments are the luster pigments, which according to DIN 55944: 2003-11 include the metallic effect pigments and the pearlescent pigments.
- Some special effect pigments can not be assigned to these two groups, eg. As platelet graphite, platelet-shaped iron oxide and micronized titanium dioxide, wherein micronized titanium dioxide produces no gloss effect, but an angle-dependent light scattering effect.
- the luster pigments according to DEST 55943: 2001-10 are predominantly platelet-shaped effect pigments. Parallel oriented luster pigments show a characteristic shine.
- the optical effect of luster pigments is based on the directed reflection of metallic particles (metallic effect pigments), on transparent particles with high refractive index (pearlescent pigments) or on the phenomenon of interference (interference pigments) (DIN 55944: 2003-1 1).
- Examples of commercially available effect pigments which are preferred according to the invention are: Timiron and # 174; from Merck, Iriodin and # 174; from Merck (pearl and color gloss pigments for decorative technical applications), Xirallic and # 174; from Merck (color intensive crystals effect pigments).
- the preparations according to the invention may advantageously also contain organic color pigments, ie organic dyes which are practically insoluble in the preparation.
- organic pigments can be prepared from chemical aspects in azo pigments and polycyclic pigments as well as according to color Be classified in terms of color or black pigments.
- the pigments can also be used advantageously in the form of commercially available oily or aqueous predispersions.
- the preparations according to the invention usually contain from 0.1 to 40% by weight.
- the preparation according to the invention contains one or more dyes.
- the dyes can be of both synthetic and natural origin. A list of suitable dyes can be found in EP 1 371 359 A2, p. 8, lines 25-57, p. 9 and p. 10, and pp. 1, lines 1 to 54, to which reference is hereby explicitly made.
- the preparations according to the invention usually contain 0.01 to 5, preferably 0.1 to 1.0 wt .-% dyes - based on the total weight of the cosmetic and / or pharmaceutical preparation.
- the preparations according to the invention usually contain a total amount of dyes and pigments in the range of 0.01 to 30 wt .-%, in particular 0.1 to 15 wt .-%, preferably 1 to 10 wt .-%, based on the total weight of the cosmetic and / or pharmaceutical preparation.
- Suitable dyes and pigments are, in particular, the dyes and pigments approved in accordance with Annex IV of the Commission Directive (in the version: Commission Directive 2007/22 / EC of 17 April 2007 amending Council Directive
- the cosmetic and / or pharmaceutical preparations may be personal care formulations, e.g. As a body milk, creams, lotions, sprayable emulsions, products for the elimination of body odor, etc.
- the hydrocarbon mixtures can also be used in surfactant-containing formulations such. B. foam and shower baths, Use shampoos and conditioners.
- the cosmetic and / or pharmaceutical preparations contain a number of other auxiliaries and additives, such as surfactants, other oil, emulsifiers, pearlescent, consistency, thickening, superfatting, stabilizers, polymers, fats, waxes, lecithins, phospholipids, biogenic agents Antidandruff agents, film formers, swelling agents, insect repellents, self-tanner, tyrosinase inhibitors (depigmenting agents), hydrotropes, solubilizers, preservatives, perfume oils, dyes, etc., which are listed below by way of example.
- auxiliaries and additives such as surfactants, other oil, emulsifiers, pearlescent, consistency, thickening, superfatting, stabilizers, polymers, fats, waxes, lecithins, phospholipids, biogenic agents Antidandruff agents, film formers, swelling agents, insect repellents, self-tanner, tyrosinase inhibitor
- An object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes, and at least one emulsifier and / or a surfactant and / or a wax component and / or a polymer and / or another oil body.
- a preferred object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes and wherein the hydrocarbons contain at least 2 mutually different hydrocarbons, the carbon number of more than 1 , preferably by 2, and at least one emulsifier and / or a surfactant and / or a wax component and / or a polymer and / or another oil body.
- the preparations according to the invention contain at least one emulsifier.
- An object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes, and at least one emulsifier.
- a preferred subject matter of the invention relates to cosmetic and / or pharmaceutical preparations containing from 0.1 to 80% by weight of hydrocarbons, one
- Hydrocarbon mixture containing 14 C isotopes and wherein the hydrocarbons contain at least 2 mutually different hydrocarbons, the carbon
- Number differs by more than 1, preferably by 2, and at least one
- Emulsifier Emulsifier.
- compositions according to the invention usually contain the emulsifier (s) in an amount of 0 to 40% by weight, preferably 0.1 to 20% by weight, preferably 0.1 to 15% by weight and in particular 0.1 to 10 wt .-% based on the emulsifier (s) in an amount of 0 to 40% by weight, preferably 0.1 to 20% by weight, preferably 0.1 to 15% by weight and in particular 0.1 to 10 wt .-% based on the
- Each emulsifier is assigned a so-called HLB value (a dimensionless number between 0 and 20) which indicates whether a preferred water or oil solubility is present.
- Numbers below 9 preferably indicate oil-soluble, hydrophobic emulsifiers, numbers over 11 water-soluble, hydrophilic emulsifiers.
- the HLB value says something about the balance of the size and strength of the hydrophilic and the lipophilic groups of an emulsifier.
- the HLB value of an emulsifier can also be calculated from increments, with the HLB increments for the different hydrophilic and hydrophobic groups that make up a molecule. As a rule, it can be taken from tables (eg H. P. Fiedler, Encyclopaedia of Pharmaceuticals, Cosmetics and Adjacent Areas, Editio Cantor Verlag, Aulendorf, 4th edition 1996) or the manufacturer's instructions.
- the solubility of the emulsifier in the two phases practically determines the type of emulsion. If the emulsifier is better soluble in water, an O / W emulsion is obtained. On the other hand, if the emulsifier has better solubility in the oiphase, a W / O emulsion is formed under otherwise identical production conditions.
- the preparation according to the invention contains more than one emulsifier.
- emulsifier such as emulsifier and co-emulsifier
- the group of nonionic emulsifiers include, for example: (1) addition products of 2 to 50 moles of ethylene oxide and / or 1 to 20 moles of propylene oxide to linear fatty alcohols having 8 to 40 carbon atoms, to fatty acids having 12 to 40 carbon atoms and to alkylphenols having 8 to 15 carbon atoms in the alkyl group.
- Alkyl mono- and oligoglycosides having 8 to 22 carbon atoms in the alkyl group and their ethoxylated analogs.
- polystyrene resin such as. Polyolpoly-12-hydroxystearate, Polyglycerinpolyricinoleat, Polyglycerindiisostearat or Polyglycerindimerat. Also suitable are mixtures of compounds of several of these classes of substances.
- partial esters based on linear, branched, unsaturated or saturated C 6 -C 22 fatty acids, ricinoleic acid and 12-hydroxystearic acid and polyglycerol, pentaerythritol, dipentaerythritol, sugar alcohols (eg sorbitol), alkyl glucosides (eg methyl glucoside , Butyl glucoside, lauryl glucoside) as well as polyglucosides (eg cellulose), or mixed esters such. Glyceryl stearate citrate and glyceryl stearate lactate.
- the addition products of ethylene oxide and / or of propylene oxide to fatty alcohols, fatty acids, alkylphenols, glycerol mono- and diesters and sorbitan mono- and diesters of fatty acids or to castor oil are known, commercially available products. These are mixtures of homologs whose mean Degree of alkoxylation Ratio of the amounts of ethylene oxide and / or propylene oxide and substrate, with which the addition reaction is carried out corresponds. Depending on the degree of ethoxylation, these are W / O or O / W emulsifiers. 2 Ci / i 8 fatty acid monoesters and diesters of addition products of ethylene oxide onto glycerol are known as refatting agents for cosmetic preparations.
- particularly useful and mild emulsifiers are polyol poly-12-hydroxystearates and mixtures thereof which, for example, under the trademarks "Dehymuls ® PGPH” (W / O-emulsifier) or “Eumulgin ® VL 75" (mixture of lauryl glucoside in a weight ratio of 1: 1, O / W emulsifier) or Dehymuls® ® SBL (W / O emulsifier) are marketed by Cognis Germany GmbH.
- the polyol component of these emulsifiers can be derived from substances which have at least two, preferably from 3 to 12 and in particular from 3 to 8 hydroxyl groups and from 2 to 12 carbon atoms.
- emulsifiers are z.
- Isolan GPS Polyhydroxystearates / sebacates
- diisostearoyl polyglyceryl-3 diisostearates eg Isolan PDI
- alkali salts acylglutamates e.g., Eumulgin SG
- HLB (100-L): 5, where L is the proportion by weight of the lipophilic groups, ie. H. the fatty alkyl or fatty acyl groups in weight percent, in the ethylene oxide adducts.
- W / O emulsifiers are partial esters of polyols, especially of C 4 -C 6 polyols, such as partial esters of pentaerythritol or sugar esters, eg. B.
- emulsifiers are addition products of from 1 to 30, preferably from 5 to 10, mol of ethylene oxide with the stated sorbitan esters.
- At least one emulsifier from the group of nonionic O / W emulsifiers (HLB value: 8-18) and / or solubilizers.
- HLB value 8-18
- solubilizers are, for example, the already mentioned in the introduction ethylene oxide adducts with a correspondingly high degree of ethoxylation, z. B. 10 - 20 ethylene oxide units for O / W emulsifiers and 20 - 40 ethylene oxide units for so-called solubilizers.
- O / W emulsifiers are ceteareth-12 and PEG-20 stearate.
- the solubilizers are preferably suitable Eumulgin ® HRE 40 (INCI: PEG-40 Hydrogenated Castor Oil), Eumulgin ® HRE 60 (INCI: PEG-60 Hydrogenated Castor Oil), Eumulgin ® L (INCI: PPG-l-PEG-9 Laurylglycolether) and Eumulgin ® SML 20 (INCI: polysorbate-20).
- Nonionic emulsifiers from the group of alkyl oligoglycosides are particularly skin-friendly and therefore preferably suitable as O / W emulsifiers.
- C 8 -C 22 alkyl mono- and oligoglycosides their preparation and their use are known from the prior art. They are prepared in particular by reacting glucose or oligosaccharides with primary alcohols having 8 to 22 carbon atoms.
- the glycoside radical both monoglycosides in which a cyclic sugar residue is glycosidically linked to the fatty alcohol and oligomeric glycosides having a degree of oligomerization of preferably approximately 8 are suitable.
- the degree of oligomerization is a statistical mean, which is based on a homolog distribution typical for such technical products.
- the glucamine-derived acylglucamides are also suitable as nonionic emulsifiers.
- Preferred according to the invention is a product which is marketed under the name Emulgade PL 68/50 by Cognis Deutschland GmbH and represents a 1: 1 mixture of alkyl polyglucosides and fatty alcohols.
- Also advantageously usable according to the invention is a mixture of lauryl glucoside, polyglyceryl-2-dipolyhydroxystearate, glycerol and water, which is commercially available under the name Eumulgin VL 75.
- suitable emulsifiers are substances such as lecithins and phospholipids.
- lecithins include the cephalins, which are also referred to as phosphatidic acids and derivatives of l, 2-diacyl-sn-glycerol-3-phosphoric acids.
- phospholipids are usually understood as meaning mono- and preferably diesters of phosphoric acid with glycerol (glycerol phosphates), which are generally regarded as fats.
- sphingosines or sphingolipids are also suitable.
- silicone emulsifiers may be included. These can be selected, for example, from the group of alkylmethicone copolyols and / or alkyl dimethicone copolyols, in particular from the group of compounds which are characterized by the following chemical structure:
- X and Y are independently selected from the group H (hydrogen) and the branched and unbranched alkyl groups, acyl groups and alkoxy groups having 1 to 24 carbon atoms, p represents a number from 0-200, q represents a number from 1-40, and r represents a number from 1-100.
- silicone emulsifiers which are particularly advantageous for the purposes of the present invention are dimethicone copolyols which have been sold by Evonik Goldschmidt under the trade names AXIL® B 8842, ABIL® B 8843, ABIL® B 8847, ABIL® B 8851, ABIL® B 8852, ABIL® B 8863, ABIL® B 8873 and ABIL® B 88183 are sold.
- a further example of surface-active substances to be used particularly advantageously in the context of the present invention is the cetyl PEG / PPG-10/1 dimethicone (Cetyl dimethicone copolyol), which is sold by Evonik Goldschmidt under the trade name ABIL® EM 90.
- a further example of surface-active substances to be used particularly advantageously for the purposes of the present invention is the cyclomethicone dimethicone copolyol, which is sold by Evonik Goldschmidt under the trade name ABIL (DEM 97 and ABIL.WE 09).
- the emulsifier Lauryl PEG / PPG-18/18 Methicone (lauryl methicone copolyol), which has been sold under the trade name Dow Corning® 5200 Formulation Aid by Dow Corning Ltd., has proved to be particularly advantageous. is available.
- Another advantageous silicone emulsifier is octyl dimethicone ethoxy glucoside from Wacker.
- water-in-silicone oil emulsion for a water-in-silicone oil emulsion according to the invention, it is possible to use all known emulsifiers used for this emulsion type.
- Particularly preferred water-in-silicone emulsifiers according to the invention are cetyl PEG / PPG-10/1 dimethicones and lauryl PEG / PPG-18/18 methicones [eg. B. ABIL® EM 90 Evonik Goldschmidt), DC5200 Formulation Aid (Dow Corning)] and any mixtures of both emulsifiers.
- the preparations according to the invention contain at least one surfactant.
- Surfactants are amphiphilic substances that can dissolve organic, nonpolar substances in water. Due to their specific molecular structure with at least one hydrophilic and one hydrophobic part of the molecule, they provide for a reduction in the surface tension of the water, the wetting of the skin, the relief of the coating and solution, a gentle rinsing off and - as desired - for foam regulation. Surfactants are usually understood to be surface-active substances which have an HLB value of greater than 20.
- An object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt .-% of a hydrocarbon mixture containing 14 C isotopes, and at least one surfactant.
- a preferred subject of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt .-% of a hydrocarbon mixture containing 14 C isotopes and wherein the hydrocarbons contain at least 2 mutually different hydrocarbons whose carbon number is more than 1, preferably 2, and at least one surfactant.
- Surfactants which may be present are anionic, nonionic, cationic and / or amphoteric or zwitterionic surfactants.
- surfactant-containing cosmetic preparations such as shower gels, foam baths, shampoos, etc., preferably at least one anionic surfactant is included.
- compositions according to the invention usually contain the surfactant (s) in an amount of 0 to 40% by weight, preferably 0.05 to 30% by weight, in particular 0.05 to 20% by weight, preferably 0.1 to 15% by weight .-% and in particular 0.1 to 10% by weight based on the total weight of the composition.
- nonionic surfactants are fatty alcohol polyglycol ethers, alkylphenol polyglycol ethers, fatty acid polyglycol ethers, fatty acid amide polyglycol ethers, fatty amine polyglycol ethers, alkoxylated triglycerides, mixed ethers, optionally partially oxidized alk (en) yloligoglycosides or glucuronic acid derivatives, fatty acid N-alkylglucamides, protein hydrolysates (in particular vegetable products Wheat base), polyol fatty acid esters, sugar esters, sorbitan esters, polysorbates and amine oxides. If the nonionic surfactants contain polyglycol ether chains can these have a conventional, but preferably a narrow homolog distribution.
- Zwitterionic surfactants are those surface-active compounds which carry at least one quaternary ammonium group and at least one -COO or -SO group in the molecule.
- Particularly suitable zwitterionic surfactants are the so-called betaines such as N-alkyl-N, N-dimethylammonium glycinates, for example cocoalkyldimethylammonium glycinate, N-acylaminopropyl-N, N-dimethylammoniumglycinates, for example cocoacylaminopropyldimethylammonium glycinate, and 2-alkyl-3-ylcinates.
- Carboxylmethyl-3-hydroxyethylimidazoline having in each case 8 to 18 carbon atoms in the alkyl or acyl group and Kokosacylaminoethylhydroxyethyl- carboxymethylglycinat.
- a preferred zwitterionic surfactant is the fatty acid amide derivative known by the INCI name Cocamidopropyl Betaine.
- ampholytic surfactants are to be understood as meaning those surface-active compounds which, apart from a Cg-C ] 8 -alkyl or acyl group in the molecule, contain at least one free amino group and at least one -COOH or -SO H group and for the formation of internal salts are capable.
- ampholytic surfactants are N-alkylglycines, N-alkylpropionic acids, N-alkylaminobutyric acids, N-alkyliminodiproic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids and alkylaminoacetic acids each having about 8 to 18 C atoms in the alkyl group.
- Particularly preferred ampholytic surfactants are N-cocoalkylaminopropionate, cocoacylaminoethyl aminopropionate and C 2-18 acyl sarcosine.
- amphoteric or zwitterionic surfactants are alkyl betaines, alkyl amidobetaines, aminopropionates, aminoglycinates, imidazolinium betaines and sulfobetaines.
- the surfactants mentioned are exclusively known compounds. As regards the structure and production of these substances, reference should be made to relevant reviews in this field.
- Typical examples of particularly suitable mild, ie particularly skin-friendly surfactants are fatty alcohol polyglycol ether sulfates, monoglyceride sulfates, mono- and / or dialkyl sulfosuccinates, fatty acid isethionates, fatty acid sarcosinates, fatty acid taurides, fatty acid glutamates, ⁇ -olefinsulfonates, ether carboxylic acids, alkyl oligoglucosides and / or mixtures thereof with alkyl oligoglucoside carboxylates, fatty acid glucamides, alkylamidobetaines, amphoacetals and / or protein fatty acid condensates, the latter preferably based on wheat proteins or their salts.
- Anionic surfactants are characterized by a water-solubilizing, anionic group such.
- Skin-compatible anionic surfactants are known to those skilled in large numbers from relevant manuals and commercially available.
- alkyl sulfates in the form of their alkali metal, ammonium or alkanolammonium salts
- alkyl ether sulfates in the form of their alkali metal, ammonium or alkanolammonium salts
- alkyl ether carboxylates acyl isethionates
- acylsarcosinates acyltaurines having linear alkyl or acyl groups having 12 to 18 carbon atoms
- sulfosuccinates and acylglutamates in the form of their alkali metal or ammonium salts.
- anionic surfactants are soaps, alkylbenzenesulfonates, alkanesulfonates, olefinsulfonates, alkyl ether sulfonates, glycerol ether sulfonates, ⁇ -methyl ester sulfonates, sulfo fatty acids, alkyl sulfates, fatty alcohol ether sulfates, glycerol ether sulfates, fatty acid ether sulfates, hydroxy mixed ether sulfates, monoglyceride (ether) sulfates, fatty acid amide (ether) sulfates , Mono- and dialkylsulfosuccinates, mono- and dialkylsulfosuccinamates, sulfotriglycerides, amide soaps, ether carboxylic acids and their salts, fatty acid isethionates, fatty acid sarcosinates,
- Quaternary ammonium compounds can be used in particular as cationic surfactants.
- ammonium halides in particular chlorides and bromides, such as alkyltrimethylammonium chlorides, dialkyldimethylammonium chlorides and trialkyl methylammonium chlorides, e.g. Cetyltrimethylammonium chloride, stearyltrimethylammonium chloride, distearyldimethylammonium chloride, lauryldimethylammonium chloride, lauryldimethylbenzylammonium chloride and tricetylmethylammonium chloride.
- the very readily biodegradable quaternary ester compounds such as the sold under the trademark Stepantex ® dialkyl ammonium methosulfates and Methylhydroxyalkyldialkoyloxyalkyl- ammonium methosulfates and the corresponding products of the Dehyquart ® series, can be used as cationic surfactants.
- the term "esterquats” is generally understood to mean quaternized fatty acid triethanolamine ester salts. They can impart a special softness to the compositions according to the invention. These are known substances which are prepared by the relevant methods of organic chemistry. Further cationic surfactants which can be used according to the invention are the quaternized protein hydrolysates.
- the preparations according to the invention contain at least one wax component.
- An object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes, and at least one wax component.
- a preferred object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes and wherein the hydrocarbons contain at least 2 mutually different hydrocarbons, the carbon number of more than 1 , preferably different by 2, and at least one wax component.
- compositions according to the invention usually contain the wax component (s) in an amount of from 0 to 40% by weight, in particular from 0 to 20% by weight, preferably from 0.1 to 15% by weight and in particular from 0.1 to 10% by weight, based on the total weight of the composition.
- wax is usually understood to mean all natural or artificially produced substances and mixtures having the following properties: they are of solid to brittle hard consistency, coarse to fine-crystalline, translucent to hazy and melt above 30 ° C. without decomposition. They are already slightly above the melting point low viscosity and non-stringy and show a strong temperature-dependent consistency and solubility. According to the invention use is a wax component or a mixture of wax components which melt at 30 0 C or above.
- Fats and fat-like substances with a waxy consistency can also be used as waxes according to the invention, as long as they have the required melting point.
- These include u.a. Fats (triglycerides), mono- and diglycerides, natural and synthetic waxes, fatty and wax alcohols, fatty acids, esters of fatty alcohols and fatty acids and fatty acid amides or any mixtures of these substances.
- Fats are triacylglycerols, ie the triple esters of fatty acids with glycerol. Preferably, they contain saturated, unbranched and unsubstituted fatty acid residues. These may also be mixed esters, ie triple esters of glycerol with different fatty acids.
- Usable according to the invention and particularly suitable as bodying agents are so-called hardened fats and oils which are obtained by partial hydrogenation. Herbal hardened fats and oils are preferred, e.g.
- Suitable include the triple esters of glycerol with C12-C60 fatty acids and in particular C12-C36 fatty acids. These include hydrogenated castor oil, a triple ester of glycerol and a Hy droxy stearic acid, for example, under the name Cutina HR in the trade. Also suitable are glyceryl tristearate, glycerol tribehenate (e.g. Syncrowax HRC), glycerol tripalmitate or the triglyceride mixtures known under the name Syncrowax HGLC, with the proviso that the melting point of the wax component or of the mixture is at 30 ° C. or above.
- glyceryl tristearate e.g. Syncrowax HRC
- glycerol tripalmitate e.g. Syncrowax HGLC
- Mono and diglycerides or mixtures of these partial glycerides can be used according to the invention as wax components.
- the glyceride mixtures which can be used according to the invention include the products marketed by Cognis GmbH & Co. KG Novata AB and Novata B (mixture of C12-C18 mono-, di- and triglycerides) and Cutina MD or Cutina GMS (glyceryl stearate).
- the fatty alcohols which can be used according to the invention as a wax component include the C12-C50 fatty alcohols.
- the fatty alcohols can be obtained from natural fats, oils and waxes, such as myristyl alcohol, 1-pentadecanol, cetyl alcohol, 1-heptadecanol, stearyl alcohol, 1-nonadecanol, arachidyl alcohol, 1-heneicosanol, behenyl alcohol, brassidyl alcohol, lignoceryl alcohol, ceryl alcohol or myricyl alcohol.
- Preferred according to the invention are saturated unbranched fatty alcohols.
- unsaturated, branched or unbranched fatty alcohols can be used according to the invention as a wax component, as long as they have the required melting point.
- Fettalkoholschnitte as used in the reduction of naturally occurring fats and oils such.
- it can also synthetic alcohols, eg.
- As the linear, even-numbered fatty alcohols of the Ziegler synthesis (Alfole) or the partially branched alcohols from the oxo synthesis (Dobanols) can be used.
- C 14-22 fatty alcohols which are particularly preferred according to the invention are C 14 -C 22 -fatty alcohols which are obtainable, for example, from Cognis Deutschland GmbH under the name Lanette 18 (C 18 -alcohol), Lanette 16 (C 16 -alcohol), Lanette 14 (C 14 -alcohol), Lanette O. (C 16 / Cl 8 alcohol) and Lanette 22 (C 18 / C22 alcohol) are marketed.
- Fatty alcohols give the compositions a drier skin sensation than triglycerides and are therefore preferred over the latter.
- wax components it is also possible to use C14-C40 fatty acids or mixtures thereof.
- B. beeswax, shellac wax, spermaceti, wool wax and raffia fat For the purposes of the invention it may be advantageous to use hydrogenated or hardened waxes.
- the natural waxes usable according to the invention also include the mineral waxes, such as.
- waxes such as ceresin and ozokerite or the petrochemical waxes such.
- petrolatum paraffin waxes and microwaxes.
- wax component and chemically modified waxes especially the hard waxes, such as.
- Montanesterwachse Sasol waxes and hydrogenated jojoba waxes used.
- the synthetic waxes which can be used according to the invention include, for example, waxy polyalkylene waxes and polyethylene glycol waxes. Vegetable waxes are preferred according to the invention.
- the wax component can also be selected from the group of wax esters of saturated and / or unsaturated, branched and / or unbranched alkanecarboxylic acids and saturated and / or unsaturated, branched and / or unbranched alcohols, from the group of esters of aromatic carboxylic acids, dicarboxylic acids, tricarboxylic acids or hydroxycarboxylic acids (for example 12-hydroxystearic acid) and saturated and / or unsaturated, branched and / or unbranched alcohols, and also from the group of the lactides of long-chain hydroxycarboxylic acids.
- esters examples include the C16-C40 alkyl stearates, C20-C40 alkyl stearates (eg Kester wax K82H), C20-C40 dialkyl esters of dimer acids, C18-C38 alkyl hydroxystearoyl stearates or C20-C40 alkyl erucates.
- Fettklandrepartialglyceride ie technical mono and / or diesters of glycerol with fatty acids having 12 to 18 carbon atoms such as glycerol mono / dilaurate, palmitate, - myristate or stearate come into question.
- Pearlescent waxes are also suitable as waxes.
- Pearlescent waxes in particular for use in surface-active formulations, are, for example: alkylene glycol esters, especially ethylene glycol distearate; Fatty acid alkanolamides, especially coconut fatty acid diethanolamide; Partial glycerides, especially stearic acid monoglyceride; Esters of polybasic, optionally hydroxy-substituted carboxylic acids with fatty alcohols having 6 to 22 carbon atoms, especially long-chain esters of tartaric acid; Fatty substances, such as fatty alcohols, fatty ketones, fatty aldehydes, fatty ethers and fatty carbonates, which in total have at least 24 carbon atoms, especially lauron and distearyl ether; Fatty acids such as stearic acid, hydroxystearic acid or behenic acid, ring-opening products of olefin epoxides having 12 to 22 carbon atoms with fatty alcohols having
- the preparations according to the invention comprise at least one polymer.
- An object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes, and at least one polymer.
- a preferred subject of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes and wherein the hydrocarbons at least 2 contain different hydrocarbons whose carbon number differs by more than 1, preferably by 2, and at least one polymer.
- compositions according to the invention usually contain the polymer (s) in an amount of from 0 to 20% by weight, preferably from 0.1 to 15% by weight and in particular from 0.1 to 10% by weight, based on the total weight of the Composition.
- Suitable cationic polymers are, for example, cationic cellulose derivatives, such as.
- a quaternized hydroxyethylcellulose obtainable under the name Polymer JR 400 ® from Amerchol, cationic starch, copolymers of diallyl ammonium salts and acrylamides, quaternized vinylpyrrolidone / vinylimidazole polymers, for example Luviquat ® (BASF), condensation products of polyglycols and amines, quaternized, collagen polypeptides, for example lauryldimonium hydroxypropyl hydrolyzed collagen (Lamequat® ® L / Grunau), quaternized wheat polypeptides, polyethyleneimine, cationic silicone polymers such.
- Suitable anionic, zwitterionic, amphoteric and nonionic polymers are, for example, vinyl acetate / crotonic acid copolymers, vinylpyrrolidone / vinyl acrylate copolymers, vinyl acetate / butyl maleate / isobornyl acrylate copolymers,
- polysaccharides especially xanthan gum, guar guar, agar agar, alginates and Tyloses and, for example, Aerosil types (hydrophilic silicas), carboxymethyl cellulose and hydroxyethyl and hydroxypropyl cellulose, polyvinyl alcohol, polyvinyl pyrrolidone and bentonites such.
- Aerosil types hydrophilic silicas
- carboxymethyl cellulose and hydroxyethyl and hydroxypropyl cellulose polyvinyl alcohol
- polyvinyl pyrrolidone polyvinyl pyrrolidone
- bentonites such as Bentone ® Gel VS-5PC (Rheox).
- quaternary polymers for example with the INCI name Polyquaternium-37, which correspond to the following general formula: xCl "
- Dialkylaminoalkyl (meth) acrylamides and their by
- Alkylation or protonation available ammonium salts can be used. Particularly preferred are polymers containing MAPTAC, APTAC,
- the preparations according to the invention comprise at least one oil body.
- the inventive Preparations the hydrocarbon mixture as oil body.
- the preparations thus contain an oil body other than the carbon mixture according to the invention, also referred to as "further oil body”.
- An object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes, and at least one a (further) oil body.
- a preferred object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes and wherein the hydrocarbons contain at least 2 mutually different hydrocarbons, the carbon number of more than 1 , preferably different by 2, and at least one (further) oil body.
- the oil bodies are usually in a total amount of 0.1-90, in particular 0.1-80, in particular 0.5 to 70, preferably 1 to 60, in particular 1 to 50 wt .-%, in particular from 1 to 40% by weight, preferably from 5 to 25% by weight and in particular from 5 to 15% by weight.
- the other oil bodies are usually present in an amount of from 0.1 to 40% by weight, based on the total weight of the preparation.
- esters of cis-Css-alkylhydroxycarboxylic acids with linear or branched C 6 -C 22 fatty alcohols in particular dioctyl malates, esters of linear and / or branched fatty acids with polyhydric alcohols (such as, for example, propylene glycol, dimerdiol or trimer triol), triglycerides based on C 6 -C 0 fatty, liquid mono- / di- / triglyceride mixtures based on C 6 -Cig-fatty acids, esters of C 6 -C 22 fatty alcohols and / or Guerbet alcohols with aromatic carboxylic acids, in particular benzoic acid, esters of C 2 -C 12 dicarboxylic acids with polyols having 2 to 10 carbon atoms and 2 to 6 hydroxyl groups, vegetable oils, branched primary alcohols, substituted cyclohexanes, linear and branched C 6 -C 22 fatty alcohol carbon
- Dicaprylyl carbonates (Cetiol® CC), Guerbetcarbonate based on fatty alcohols having 6 to 18, preferably 8 to 10 C atoms, esters of benzoic acid with linear and / or branched C 6 -C 22 alcohols (eg Finsolv® TN), linear or branched, symmetrical or asymmetrical dialkyl ethers having 6 to 22 carbon atoms per alkyl group, such as.
- dicaprylyl (Cetiol® OE)
- ring-opening products of epoxidized fatty acid esters with polyols and hydrocarbons or mixtures thereof As dicaprylyl (Cetiol® OE), ring-opening products of epoxidized fatty acid esters with polyols and hydrocarbons or mixtures thereof.
- silicone oils come into question. They can be present as cyclic and / or linear silicone oils. Silicone oils are high molecular weight synthetic polymeric compounds in which silicon atoms are chain and / or netlike linked via oxygen atoms and the remaining valencies of silicon are linked by hydrocarbon radicals (usually methyl, more rarely ethyl, propyl, phenyl groups, etc.) are saturated. Systematically, the silicone oils are called polyorganosiloxanes. The methyl-substituted polyorganosiloxanes, which are the quantitatively most important compounds of this group and are represented by the following structural formula
- Dimethicones are available in different chain lengths or with different molecular weights.
- poly(dimethylsiloxane) are, for example, dimethylpolysiloxane [poly (dimethylsiloxane)], which are obtainable, for example, under the trade names Abil 10 to 10,000 from Evonik Goldschmidt.
- phenylmethylpolysiloxane phenyl dimethicone, phenyl trimethicone
- cyclic silicones octamethylcyclotetrasiloxane or decamethylcyclopentasiloxane
- INCI cyclomethicone
- amino-modified silicones INCI: Amodimethicone
- silicone waxes eg.
- Polysiloxane-polyalkylene copolymers (INCI: stearyl dimethicone and cetyl dimethicone) and dialkoxydimethylpolysiloxanes (stearoxy dimethicone and behenoxy stearyl dimethicone) available as various Abil-Wax types from Evonik Goldschmidt.
- other silicone oils are also advantageous for the purposes of the present invention, for example cetyidimethicone, hexamethylcyclo- trisiloxane, polydimethylsiloxane, poly (methylphenylsiloxane).
- Particularly preferred silicones according to the invention are dimethicone and cyclomethicone.
- the preparations according to the invention may furthermore contain biogenic active compounds, insect repellents, tyrosinase inhibitors, preservatives, perfume oils, superfatting agents, stabilizers and / or hydrotropes.
- An object of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes, and at least one biogenic agent, insect repellent, tyrosinase inhibitor, preservative, perfume oil, stabilizer and / or hydrotrope.
- a preferred subject of the invention relates to cosmetic and / or pharmaceutical preparations containing 0.1 to 80 wt.% Of a hydrocarbon mixture containing 14 C isotopes and wherein the hydrocarbons contain at least 2 mutually different hydrocarbons whose carbon number to more than 1, preferably 2, and at least one biogenic active ingredient, insect repellent, tyrosinase inhibitor, preservative, perfume oil, stabilizer and / or hydrotrope.
- biogenic active substances include tocopherol, tocopherol acetate, tocopherol palmitate, ascorbic acid, (deoxy) ribonucleic acid and their fragmentation products, ⁇ -glucans, retinol, bisabolol, allantoin, phytantriol, panthenol, AHA acids, amino acids, ceramides, pseudoceramides, essential oils, plant extracts, such as As aloe vera, Prunusex Consumer, Bambaranussex Exercise and vitamin complexes to understand.
- Suitable insect repellents are N, N-diethyl-m-toluamide, 1,2-pentanediol or ethyl 3- (Nn-butyl-N-acetyl-amino) -propionic acid ethyl ester), which under the name ® Insect Repellent 3535 by Merck KGaA is sold, as well as Butylacetylaminopropionate in question.
- Tyrosinhinbitoren that prevent the formation of melanin and find application in depigmenting, for example, arbutin, ferulic acid, kojic acid, coumaric acid and ascorbic acid (vitamin C) come into question.
- Suitable preservatives are, for example, phenoxyethanol, formaldehyde solution, parabens, pentanediol or sorbic acid and also the silver complexes known under the name Surfacine®. Also suitable as preservatives are the 1,2-alkanediols having 5 to 8 C atoms described in WO07 / 048757.
- Particularly suitable preservatives are those described in Annex VI of the Commission Directive (as amended by Commission Directive 2007/22 / EC of 17 April 2007 amending Council Directive 76/768 / EEC, concerning cosmetic products, for the purposes of adapting Annexes IV and VI to technical progress) substances, which are explicitly referred to here.
- Natural fragrances are extracts of flowers, stems and leaves, fruits, fruit peel, roots, woods, herbs and grasses, needles and twigs, resins and balsams. Furthermore, animal raw materials, such as civet and Castoreum and synthetic fragrance compounds of the ester type, ethers, aldehydes, ketones, alcohols and hydrocarbons come into question.
- metal salts of fatty acids such as.
- magnesium, aluminum and / or zinc stearate or ricinoleate can be used.
- Hydrotropes such as, for example, ethanol, isopropyl alcohol, or polyols can also be used to improve the flow behavior.
- Polyols contemplated herein preferably have from 2 to 15 carbon atoms and at least two hydroxyl groups.
- the polyols may contain other functional groups, in particular amino groups, or be modified with nitrogen.
- GC analysis shows the following composition: 89.0% tridecane, 2.1% tetradecane, 4.1% 1-tetradecanol, 4.2% dimeric reaction products. This reaction product was fractionated in a distillation to pure tridecane and then deodorized with nitrogen. This gives a colorless, low viscosity and low odor product.
- Composition of the hydrocarbon mixture according to Example 1 76% by weight of n-undecane, 24% by weight of n-tridecane.
- a fatty alcohol mixture containing C 12 and C 14 fatty alcohols corresponding to the hydrocarbon mixture to be prepared was subjected to reductive dehydroxymethylation:
- the hydrocarbon mixture obtainable according to Preparation Example 2 is composed as follows: (GC analysis)
- the weight ratio of linear C11 hydrocarbon to linear C13 hydrocarbon is 2.57.
- the weight ratio of the C 12 hydrocarbons to the C 14 hydrocarbons is 2.57.
- the hydrocarbon mixture obtainable according to Preparation Example 3 is composed as follows: (GC analysis) C 11 hydrocarbon 55%, C 13 hydrocarbon 20%, C 15 hydrocarbon 10%, C 17 hydrocarbon 15%.
- the reactor is closed and evacuated.
- the reaction mixture is then heated under vacuum to about 80 ° C and 30 min. touched. Thereafter, the reactor is brought to about 80 bar with hydrogen and continuously heated to 250 ° C.
- the reaction is complete when the pressure remains constant and most of the fatty alcohol is converted to the desired hydrocarbon.
- the product is purified by distillation. The purified product is obtained as a colorless liquid.
- the hydrocarbon mixture obtainable according to preparation example 4 A is composed as follows: (GC analysis) C 15 hydrocarbon 65%, C 17 hydrocarbon
- the hydrocarbon mixture obtainable according to preparation example 4 B is composed as follows: (GC analysis) C 15 hydrocarbon 50%, C 17 hydrocarbon 50%.
- the hydrocarbon mixture obtainable according to preparation example 4 C is composed as follows: (GC analysis) C 15 hydrocarbon 30%, C 17 hydrocarbon 70%.
- the reactor is closed and evacuated.
- the reaction mixture is then submerged Vacuum heated to about 80 ° C and 30 min. touched. Thereafter, the reactor is brought to about 80 bar with hydrogen and continuously heated to 250 ° C.
- the reaction is complete when the pressure remains constant and most of the fatty alcohol is converted to the desired hydrocarbon.
- the product is purified by distillation. The purified product is obtained as a colorless liquid.
- the hydrocarbon mixture obtainable according to Preparation Example 5 A is composed as follows: (GC analysis) C 17 hydrocarbon 45%, C 19 hydrocarbon 10%, C 21 hydrocarbon 45%.
- the hydrocarbon mixture obtainable according to Preparation Example 5 B is composed as follows: (GC analysis) C 17 hydrocarbon 40%, C 19 hydrocarbon 12%, C 21 hydrocarbon 48%.
- the hydrocarbon mixture obtainable according to preparation example 5 C is composed as follows: (GC analysis) C 17 hydrocarbon 10%, C 19 hydrocarbon 15%, C 21 hydrocarbon 75%.
- the hardness was determined according to the German standard methods for the investigation of fats, fat products, surfactants and related substances, determination of the hardness of waxes. Needle Penetration M-III 9b (98)
- phase I The components of phase I were melted at 80 to 85 ° C and stirred to homogeneity.
- the components of phase II were heated to 80 to 85 ° C and added slowly to phase I with stirring. It was stirred for a further 5 minutes at this temperature. Thereafter, the emulsion was cooled with stirring and homogenized at 65 to 55 ° C. As soon as the emulsion appears homogeneous, it was further cooled to 30 ° C. with stirring. Thereafter, phase III components were added and stirred again.
- Phase I was melted at 85 ° C, Phase II was added and the temperature maintained at 80 ° C. Phase III was added shortly before pouring into the mold (which had been moistened with dimethicone 50 cts and preheated to 40 ° C). The mass was placed in the mold and cooled to 40 ° C. The molds were cooled in the freezer to near 0 0 C.
- the preparation is carried out by heating all components to 80 ° C and homogenization.
- phase II The preparation was carried out by mixing phase I and water at room temperature with stirring. Then, Phase III was added and stirred until a homogeneous, swollen mixture was present. Then, Phase IV was added, followed by Phase V, then the pH was adjusted.
- This cream was prepared by heating Phase I to 80 ° C, Phase II was also heated to 80 ° C and added to Phase I with stirring. This mixture was cooled with stirring and homogenized at about 55 ° C with a suitable dispersion device (eg Ultra Turrax). Thereafter, Phase III was added with continuous stirring, Phase IV was added and the pH was adjusted.
- a suitable dispersion device eg Ultra Turrax
- the first 7 components were melted at 85 ° C. Magnesium sulfates and glycerine were dissolved in the water and this mixture was heated to 85 ° C. This aqueous phase was added to the oil phase and dispersed. With continuous stirring, it was cooled to 40 ° C and then benzyl alcohol and Hydagen B were mixed and added to the emulsion. With further stirring was cooled to 30 ° C and homogenized.
Abstract
Description
Claims
Priority Applications (5)
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US12/665,493 US8956598B2 (en) | 2007-06-19 | 2008-06-12 | Hydrocarbon mixtures and use thereof |
CN200880021261.4A CN101677923B (en) | 2007-06-19 | 2008-06-12 | Hydrocarbon mixtures and use thereof |
EP08759204A EP2162114A2 (en) | 2007-06-19 | 2008-06-12 | Hydrocarbon mixtures and use thereof |
JP2010512573A JP5944100B2 (en) | 2007-06-19 | 2008-06-12 | Hydrocarbon mixtures and uses thereof |
ZA2009/09059A ZA200909059B (en) | 2007-06-19 | 2009-12-18 | Hydrocarbon mixtures and use thereof |
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EP07011967A EP2014274A1 (en) | 2007-06-19 | 2007-06-19 | Hydrocarbon compounds and their use |
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EP07075513 | 2007-06-20 | ||
EPEP07075513 | 2007-06-20 | ||
DE102008012458.3 | 2008-03-04 | ||
DE102008012458 | 2008-03-04 | ||
DE102008017032 | 2008-04-03 | ||
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DE102008017032.1 | 2008-04-03 |
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DE102019135833A1 (en) * | 2019-12-27 | 2021-07-01 | Henkel Ag & Co. Kgaa | Antiperspirant cosmetic without cyclic silicone oils |
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FR3108256A1 (en) | 2020-03-23 | 2021-09-24 | L'oreal | REACTIVE TWO-STEP LIP SYSTEM |
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WO2021191548A1 (en) | 2020-03-23 | 2021-09-30 | Roquette Freres | Emulsifying and texturing composition based on starches and gums, for cosmetics |
WO2021202156A1 (en) | 2020-03-31 | 2021-10-07 | L'oreal | Mattifying nail compositions |
FR3109313A1 (en) | 2020-04-15 | 2021-10-22 | L'oréal | PROCESS FOR TREATMENT OF KERATINIC MATERIALS USING AN ACRYLIC ANHYDRIDE POLYMER IN OILY DISPERSION AND A HYDROXYL AND / OR THIOLE COMPOUND |
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FR3109882A1 (en) | 2020-05-06 | 2021-11-12 | L'oreal | Mattifying compositions for nails |
FR3110840A1 (en) | 2020-05-29 | 2021-12-03 | L'oreal | COMPOSITION FOR TAKING CARE OF AND / OR MAKE-UP OF KERATIN-BASED MATERIALS |
FR3111074A1 (en) | 2020-06-08 | 2021-12-10 | L'oreal | Retinol-based composition |
FR3111075A1 (en) | 2020-06-08 | 2021-12-10 | L'oreal | Retinol-based composition |
FR3111558A1 (en) | 2020-06-23 | 2021-12-24 | L'oreal | Process for treating keratin fibers comprising the application of a makeup removing composition, the keratin fibers having been previously colored |
FR3111556A1 (en) | 2020-06-18 | 2021-12-24 | L'oreal | Composition comprising polymer particles, a volatile hydrocarbon-based oil, a film-forming silicone vinyl polymer, a coconut oil |
FR3111557A1 (en) | 2020-06-23 | 2021-12-24 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer comprising at least two different polymer units with a (un) saturated hydrocarbon chain in a fatty medium |
WO2021260078A1 (en) | 2020-06-24 | 2021-12-30 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer bearing a(n) (un)saturated hydrocarbon-based chain and a surfactant |
WO2021260079A1 (en) | 2020-06-24 | 2021-12-30 | L'oreal | Cosmetic composition comprising a grafted polyhydroxyalkanoate copolymer in a fatty medium |
FR3111799A1 (en) | 2020-06-30 | 2021-12-31 | L'oreal | Composition comprising a combination of polyglycerol esters |
FR3111801A1 (en) | 2020-06-30 | 2021-12-31 | L'oreal | Coloring and / or lightening composition comprising an anthraquinone cationic direct dye, a fatty substance, a chemical oxidizing agent and an alkaline agent and / or an oxidation dye precursor |
FR3111810A1 (en) | 2020-06-30 | 2021-12-31 | L'oreal | Composition comprising a combination of fillers |
WO2022003000A1 (en) | 2020-07-01 | 2022-01-06 | L'oreal | Two-phase composition comprising an alkylpolyglycoside surfactant, a particular diol and an alkane, ester or ether compound comprising from 15 to 30 carbon atoms |
WO2022008691A1 (en) | 2020-07-10 | 2022-01-13 | L'oreal | Water-in-oil emulsion having a high internal water phase content |
WO2022084458A1 (en) | 2020-10-23 | 2022-04-28 | L'oreal | Photoprotective composition |
FR3117032A1 (en) | 2020-12-08 | 2022-06-10 | L'oreal | Gel composition comprising silica airgel and ethylguar as thickening agents |
FR3117366A1 (en) | 2020-12-14 | 2022-06-17 | L'oreal | Cosmetic composition comprising at least one hydrocarbon oil and from 4% to 15% by weight of at least one wax chosen from Candelilla wax, Carnauba wax and mixtures thereof |
WO2022129039A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Cosmetic composition comprising a merocyanine, a triazine uv-screening agent, and a polysaccharide modified with hydrophobic chains |
WO2022129059A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Cosmetic or dermatological composition comprising a merocyanine and an oily phase comprising at least one citric acid ester |
WO2022129195A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Dispersion comprising a polymeric particle, a stabilizer bearing a c3-c12 cycloalkyl group, an oil and water, and process for treating keratin materials using the dispersion |
WO2022129403A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Composition comprising aqueous gelling agents, surfactants and ascorbic acid |
WO2022129192A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Dispersion comprising a polymeric particle, a stabilizer bearing a c9-c22 alkyl group, an oil and water, and process for treating keratin materials using the dispersion |
WO2022129477A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Composition comprising aqueous gelling agents, a surfactant, oils, fillers and ascorbic acid |
WO2022129469A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Composition comprising aqueous gelling agents, a surfactant and ascorbic acid |
WO2022128544A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Cosmetic composition comprising an oily dispersion of polymer particles and an aqueous dispersion of colloidal silica particles |
WO2022128901A1 (en) | 2020-12-17 | 2022-06-23 | L'oreal | Process for dyeing keratin fibres using two different compounds that are capable of forming covalent bonds together and also a particular metal salt or a salt of a metal belonging to the rare-earth metal group or a particular organometallic compound |
FR3117852A1 (en) | 2020-12-23 | 2022-06-24 | L'oréal | Cosmetic composition comprising a copolymer based on acetoacetate functions |
FR3117862A1 (en) | 2020-12-22 | 2022-06-24 | L'oreal | COMPOSITION FOR THE CARE AND/OR MAKEUP OF KERATINOUS MATERIALS |
FR3117794A1 (en) | 2020-12-23 | 2022-06-24 | L'oreal | Aqueous dispersion of a specific copolymer and its cosmetic applications |
FR3117849A1 (en) | 2020-12-17 | 2022-06-24 | L'oreal | Process for dyeing keratinous fibers using two distinct compounds capable of forming covalent bonds together as well as a particular metal salt |
FR3117853A1 (en) | 2020-12-23 | 2022-06-24 | L'oreal | Cosmetic composition comprising polymeric particles based on acetoacetate functions |
FR3117796A1 (en) | 2020-12-22 | 2022-06-24 | L'oreal | Gelled aqueous composition comprising a magnesium salt |
FR3117787A1 (en) | 2020-12-22 | 2022-06-24 | L'oreal | Gelled aqueous composition comprising a heavy grade magnesium salt |
FR3117856A1 (en) | 2020-12-23 | 2022-06-24 | L'oréal | Cosmetic composition comprising a block copolymer based on acetoacetate functions |
FR3117797A1 (en) | 2020-12-22 | 2022-06-24 | L'oreal | Anhydrous deodorant oily composition with dry and fresh effect sprayable without propellant gas |
FR3117851A1 (en) | 2020-12-17 | 2022-06-24 | L'oreal | Process for dyeing keratin fibers using two distinct compounds capable of forming covalent bonds together as well as a particular organometallic compound |
FR3117789A1 (en) | 2020-12-22 | 2022-06-24 | L'oreal | Cosmetic composition comprising at least one clay, at least one crystallizable fatty substance and at least one fat-soluble UV filter |
FR3117867A1 (en) | 2020-12-22 | 2022-06-24 | L'oreal | Natural wax microdispersion |
FR3117798A1 (en) | 2020-12-18 | 2022-06-24 | L'oreal | Cosmetic composition an oily dispersion of polymer particles and an aqueous dispersion of film-forming polymer particles not derived from styrenic monomer. |
FR3117850A1 (en) | 2020-12-17 | 2022-06-24 | L'oreal | Process for dyeing keratin fibers using two distinct compounds capable of forming covalent bonds together and a metal salt belonging to the rare earth group |
FR3117785A1 (en) | 2020-12-18 | 2022-06-24 | L'oreal | Cosmetic composition comprising an oily dispersion of polymer particles and an aqueous microdispersion of wax particles. |
WO2022136114A1 (en) | 2020-12-23 | 2022-06-30 | L'oreal | Aqueous dispersion of a specific copolymer, and cosmetic uses thereof |
WO2022136104A1 (en) | 2020-12-23 | 2022-06-30 | L'oreal | Cosmetic composition comprising a copolymer based on acetoacetate functions |
WO2022136110A1 (en) | 2020-12-23 | 2022-06-30 | L'oreal | Cosmetic composition comprising polymer particles based on acetoacetate functions |
FR3118701A1 (en) | 2021-01-12 | 2022-07-15 | L'oreal | BIPHASIC COMPOSITION FOR CLEANSING AND/OR MAKE-UP REMOVAL OF KERATINOUS MATERIALS |
FR3118706A1 (en) | 2021-01-12 | 2022-07-15 | L'oreal | BIPHASIC COMPOSITION FOR CLEANSING AND/OR MAKE-UP REMOVAL OF KERATINOUS MATERIALS |
FR3119988A1 (en) | 2021-02-25 | 2022-08-26 | L'oreal | Aqueous composition comprising an organic UV filter, a superabsorbent polymer, perlite and a fatty alcohol |
WO2022189573A1 (en) | 2021-03-10 | 2022-09-15 | L'oreal | Hair colouring composition comprising at least one (poly)carbodiimide compound and at least one compound comprising at least one hydroxyl function |
WO2022189571A1 (en) | 2021-03-10 | 2022-09-15 | L'oreal | Process for removing the colour from hair keratin fibers which have been coloured beforehand with a specific hair colouring composition |
WO2022189570A1 (en) | 2021-03-10 | 2022-09-15 | L'oreal | Process for colouring hair keratin fibers, comprising the application of a composition comprising at least one (poly)carbodiimide compound and a composition comprising at least one associative polymer and a particular compound |
WO2022189576A1 (en) | 2021-03-10 | 2022-09-15 | L'oreal | Hair colouring composition comprising at least one (poly)carbodiimide compound and at least one non-carboxylic anionic thickener |
WO2022189575A1 (en) | 2021-03-10 | 2022-09-15 | L'oreal | Process for colouring hair keratin fibers comprising the application of a composition comprising at least one (poly)carbodiimide compound and a composition comprising at least one associative polymer and a particular compound |
WO2022189572A1 (en) | 2021-03-10 | 2022-09-15 | L'oreal | Process for removing the colour from previously coloured hair keratin fibers |
FR3122336A1 (en) | 2021-04-30 | 2022-11-04 | L'oreal | anhydrous composition for caring for and/or making up keratin materials |
FR3123567A1 (en) | 2021-06-07 | 2022-12-09 | L'oreal | Hair coloring process comprising the application of a (poly)carbodiimide compound, a polymer containing a carboxylic group and a non-silicone fatty substance |
WO2022263603A1 (en) | 2021-06-16 | 2022-12-22 | L'oreal | Composition comprising an oily dispersion of polymer particles, a cationic polymer and an anionic polymer |
FR3124081A1 (en) | 2021-06-21 | 2022-12-23 | L'oreal | Cosmetic composition comprising at least one polar oil, one polyol and at least one hydrophilic active |
FR3124698A1 (en) | 2021-06-30 | 2023-01-06 | L'oreal | Composition comprising at least one UV screening agent, boron nitride, and a nonionic surfactant of ester type |
WO2023036686A1 (en) | 2021-09-10 | 2023-03-16 | L'oreal | Makeup kit comprising an aqueous makeup composition and a continuous oily-phase fixing composition with a hydrophobic film-forming polymer |
FR3127398A1 (en) | 2021-09-30 | 2023-03-31 | L'oreal | Cosmetic composition comprising at least one polar oil, one polyol and ascorbic acid |
FR3127695A1 (en) | 2021-10-05 | 2023-04-07 | L'oreal | OILY DISPERSION COMPRISING A POLYMERIC PARTICLE, A STABILIZING AGENT WITH A C9-C22 ALKYL GROUP, AND A PLASTICIZER METHOD FOR TREATMENT OF KERATIN MATERIALS USING THE OILY DISPERSION |
FR3129596A1 (en) | 2021-12-01 | 2023-06-02 | L'oreal | Process for dyeing keratinous fibers using a compound bearing a reactive chemical function, an alkoxysilane, a coloring agent and optionally a compound chosen from metal salts, metal compounds belonging to the group of rare earths and metal alkoxides |
FR3129597A1 (en) | 2021-12-01 | 2023-06-02 | L'oreal | Process for treating keratin fibers using an acrylate functionalized polymer and an alkoxysilane |
FR3129832A1 (en) | 2021-12-06 | 2023-06-09 | L'oreal | Non-silicone inverse emulsion comprising a C3 or C4 alkanediol, glycerin, a non-volatile vegetable oil, a polyglyceryl polyricinoleate surfactant and a volatile alkane |
WO2023104924A1 (en) | 2021-12-09 | 2023-06-15 | L'oreal | Composition comprising a combination of polyglycerol esters and a filler |
WO2023104727A1 (en) | 2021-12-09 | 2023-06-15 | L'oreal | Dispersion comprising a polymeric particle, a stabilizer bearing a cycloalkyl group, an oil and a polyol, and process for treating keratin materials using the dispersion |
WO2023107199A1 (en) | 2021-12-09 | 2023-06-15 | L'oreal | Skin perfecting cosmetic compositions and methods of use |
WO2023104730A1 (en) | 2021-12-09 | 2023-06-15 | L'oreal | Dispersion comprising a polymeric particle, a stabilizer bearing a cycloalkyl group, an oil and water, and process for treating keratin materials using the dispersion |
FR3130135A1 (en) | 2021-12-15 | 2023-06-16 | L'oreal | Water-in-oil emulsion without silicone compounds comprising an alkylpolyglucoside surfactant, a surfactant mono- and di-polyethoxylated esters of hydroxy acids, ester oils and ester hydrocarbon waxes |
FR3130158A1 (en) | 2021-12-14 | 2023-06-16 | L'oreal | Cosmetic composition comprising a bis-amino silicone, a cationic surfactant, a fatty alcohol and a fatty alkane, cosmetic treatment method and use |
FR3130159A1 (en) | 2021-12-14 | 2023-06-16 | L'oreal | Cosmetic composition comprising a bis-amino silicone, a cationic surfactant, a fatty alcohol and a fatty alcohol ester, cosmetic treatment method and use |
FR3130157A1 (en) | 2021-12-15 | 2023-06-16 | L'oreal | REMOVABLE MAKE-UP REMOVER COMPOSITIONS |
WO2023111269A1 (en) | 2021-12-16 | 2023-06-22 | L'oreal | Process for colouring the hair, comprising at least the application of a composition comprising a (poly)carbodiimide compound, a silicone acrylic copolymer and at least one colouring agent |
WO2023110770A1 (en) | 2021-12-17 | 2023-06-22 | L'oreal | Cosmetic or dermatological composition comprising a merocyanine and dipropylene glycol |
WO2023110764A1 (en) | 2021-12-17 | 2023-06-22 | L'oreal | Cosmetic or dermatological composition comprising a merocyanine and resveratrol and/or a resveratrol derivative |
WO2023111079A1 (en) | 2021-12-17 | 2023-06-22 | L'oreal | Process for dyeing keratin fibres using a (co)polymer based on acetoacetate functions, a crosslinking agent, a colouring agent and a metal compound |
WO2023110754A1 (en) | 2021-12-16 | 2023-06-22 | L'oreal | Process for colouring the hair comprising the application of a (poly)carbodiimide compound, a silicone acrylic copolymer, a surfactant and a colouring agent |
WO2023110767A1 (en) | 2021-12-17 | 2023-06-22 | L'oreal | Cosmetic or dermatological composition comprising a merocyanine and a gamma-butyrolactone and/or a gamma-butyrolactam |
WO2023110772A1 (en) | 2021-12-17 | 2023-06-22 | L'oreal | Cosmetic or dermatological composition comprising at least a merocyanine and a hydrotrope |
WO2023110773A1 (en) | 2021-12-17 | 2023-06-22 | L'oreal | Cosmetic or dermatological composition comprising a merocyanine and at least one diol comprising from 4 to 7 carbon atoms |
WO2023111081A1 (en) | 2021-12-17 | 2023-06-22 | L'oreal | Process for dyeing keratin fibres using a copolymer based on acetoacetate functions, a crosslinking agent, a colouring agent and a metal compound |
WO2023111268A1 (en) | 2021-12-16 | 2023-06-22 | L'oreal | Hair dyeing process, comprising the application of a (poly)carbodiimide compound of specific formula, a silicone acrylic polymer, two compounds with specific hansen solubility parameters and a colouring agent |
WO2023110763A1 (en) | 2021-12-17 | 2023-06-22 | L'oreal | Cosmetic and/or dermatological composition comprising at least one merocyanine and at least ascorbic acid and/or a derivative thereof |
WO2023110777A1 (en) | 2021-12-17 | 2023-06-22 | L'oreal | Cosmetic or dermatological composition comprising a merocyanine and pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate |
FR3130599A1 (en) | 2021-12-17 | 2023-06-23 | L'oreal | Cosmetic or dermatological composition comprising a merocyanin and a gamma-butyrolactone and/or a gamma-butyrolactam |
FR3130611A1 (en) | 2021-12-20 | 2023-06-23 | L'oreal | Polyhydroxyalkanoate copolymer with acetoacetate group, composition containing it and its use in cosmetics |
FR3130608A1 (en) | 2021-12-21 | 2023-06-23 | L'oreal | Cosmetic composition comprising a particulate cellulosic compound, hydrophobic silica airgel particles, a semi-crystalline polymer and a wax of plant origin |
FR3130606A1 (en) | 2021-12-21 | 2023-06-23 | L'oreal | Cosmetic composition comprising a particulate cellulosic compound, particles of hydrophobic silica airgel, and a wax of plant origin |
FR3130615A1 (en) | 2021-12-16 | 2023-06-23 | L'oreal | Hair coloring process comprising the application of a (poly)carbodiimide compound, a silicone acrylic copolymer and a coloring agent |
FR3130581A1 (en) | 2021-12-21 | 2023-06-23 | L'oreal | COSMETIC COMPOSITION CONTAINING A COMBINATION OF VANILLIN OR ONE OF ITS DERIVATIVES, AROMATIC ALCOHOL AND ALIPHATIC MONOALCOOL |
FR3130605A1 (en) | 2021-12-21 | 2023-06-23 | L'oreal | Cosmetic composition comprising a particulate cellulosic compound, hydrophobic silica airgel particles, and a semi-crystalline polymer |
FR3130560A1 (en) | 2021-12-17 | 2023-06-23 | L'oreal | Composition comprising a combination of polyglycerol esters, a mineral UV filter and a liposoluble or specific hydrophobic particulate coloring matter |
FR3130614A1 (en) | 2021-12-16 | 2023-06-23 | L'oreal | Hair coloring process comprising at least the application of a composition comprising a (poly)carbodiimide compound, a silicone acrylic copolymer and at least one coloring agent |
FR3130573A1 (en) | 2021-12-17 | 2023-06-23 | L'oreal | COSMETIC COMPOSITION COMPRISING A PATTERNED ALKYL-AZLACTONE COPOLYMER AND USES THEREOF |
FR3130610A1 (en) | 2021-12-20 | 2023-06-23 | L'oreal | Composition comprising a polyhydroxyalkanoate copolymer with a long hydrocarbon chain containing ionic group(s), process for treating keratin materials using the composition |
WO2023118524A1 (en) | 2021-12-23 | 2023-06-29 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer bearing a (un)saturated hydrocarbon-based chain and a modified polysaccharide |
WO2023118529A1 (en) | 2021-12-23 | 2023-06-29 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer bearing a(n) (un)saturated hydrocarbon-based chain and a natural resin |
WO2023118467A1 (en) | 2021-12-23 | 2023-06-29 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer bearing a(n) (un)saturated hydrocarbon-based chain and a crystallizable fatty substance |
WO2023118481A1 (en) | 2021-12-23 | 2023-06-29 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer bearing a(n) (un)saturated hydrocarbon-based chain and a mixture of volatile oil and non-volatile oil |
WO2023118430A1 (en) | 2021-12-23 | 2023-06-29 | L'oreal | Cosmetic composition comprising a natural resin |
WO2023118530A1 (en) | 2021-12-23 | 2023-06-29 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer bearing a(n) (un)saturated hydrocarbon-based chain and a silicone polymer |
WO2023118528A1 (en) | 2021-12-23 | 2023-06-29 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer bearing a(n) (un)saturated hydrocarbon-based chain and a polysaccharide |
WO2023118427A1 (en) | 2021-12-23 | 2023-06-29 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer bearing a(n) (un)saturated hydrocarbon-based chain and a clay |
WO2023118526A1 (en) | 2021-12-23 | 2023-06-29 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer bearing a (un)saturated hydrocarbon-based chain and a hydrocarbon-based polymer |
WO2023118523A1 (en) | 2021-12-23 | 2023-06-29 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer bearing a (un)saturated hydrocarbon-based chain and an oligo/polyester |
FR3131204A1 (en) | 2021-12-23 | 2023-06-30 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer with an (un)saturated hydrocarbon chain, and a plasticizer |
FR3131208A1 (en) | 2021-12-23 | 2023-06-30 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer with an (un)saturated hydrocarbon chain, and at least one polyurethane latex |
WO2023126397A1 (en) | 2021-12-31 | 2023-07-06 | L'oreal | Kit for customizing a cosmetic composition |
FR3132220A1 (en) | 2022-01-31 | 2023-08-04 | L'oreal | skin-perfecting cosmetic compositions and methods of use |
FR3132637A1 (en) | 2022-02-15 | 2023-08-18 | L'oreal | Cosmetic or dermatological composition comprising a merocyanine and a polyionic complex |
WO2023170236A1 (en) | 2022-03-10 | 2023-09-14 | L'oreal | Composition comprising at least one amps® copolymer, at least one alkyl(poly)glycoside, at least one uv-screening agent and isopropyl myristate |
WO2023180256A1 (en) | 2022-03-22 | 2023-09-28 | L'oreal | Composition comprising ethyl cellulose, a monoalcohol, a volatile hydrocarbon-based oil, a non-volatile alkane oil, a mono- or di-ester of a fatty acid and of polyglycerol and an ester oil |
FR3133751A1 (en) | 2022-03-22 | 2023-09-29 | L'oreal | Composition comprising ethyl cellulose, a mono-alcohol, a volatile hydrocarbon oil, a non-volatile alkane oil, a mono- or di-ester of fatty acid and polyglycerol and an ester oil |
FR3133754A1 (en) | 2022-03-22 | 2023-09-29 | L'oreal | Composition comprising ethyl cellulose, a mono-alcohol, a volatile hydrocarbon oil, a non-volatile alkane oil, a mono- or diester of fatty acid and polyglycerol and an alkyl benzoate |
FR3133753A1 (en) | 2022-03-22 | 2023-09-29 | L'oreal | Composition comprising ethyl cellulose, a mono-alcohol, a volatile hydrocarbon oil, a non-volatile alkane oil, a mono- or diester of fatty acid and polyglycerol and a dialkyl carbonate |
FR3133752A1 (en) | 2022-03-22 | 2023-09-29 | L'oreal | Composition comprising ethyl cellulose, a mono-alcohol, a volatile hydrocarbon oil, a non-volatile alkane, a polyglycerol fatty acid ester and a linoleic or oleic acid ester |
WO2023194239A1 (en) | 2022-04-08 | 2023-10-12 | L'oreal | Inverse emulsion comprising a dextrin ester, a volatile linear alkane, a natural wax, a natural hydrophilic polymeric gelling agent, and a non-ionic emulsifier |
WO2023198923A1 (en) | 2022-04-15 | 2023-10-19 | L'oreal | Direct emulsion comprising a uv-screening agent, a lipophilic acrylic polymer, a fatty acid ester of a polyol and a carboxylic anionic surfactant |
FR3134516A1 (en) | 2022-04-15 | 2023-10-20 | L'oreal | Direct emulsion comprising a UV filter, a lipophilic acrylic polymer, a polyol fatty acid ester and an amino acid derivative |
FR3134517A1 (en) | 2022-04-19 | 2023-10-20 | L'oreal | Reverse emulsion for skin care |
WO2023208677A1 (en) | 2022-04-28 | 2023-11-02 | L'oreal | Inverse emulsion comprising a polyphenol, a non-ionic polysaccharide, a polyglycerolated non-ionic surfactant with an hlb ≤ 8, a polyol, a non-volatile plant oil, and a volatile alkane |
WO2023230311A1 (en) | 2022-05-27 | 2023-11-30 | L'oréal | Adhesive mascara compositions |
FR3136369A1 (en) | 2022-06-08 | 2023-12-15 | L'oreal | EYEBROW PRIMER |
WO2023247575A1 (en) | 2022-06-20 | 2023-12-28 | L'oreal | Composition comprising at least one glycolipid, at least one linear or branched liquid fatty alcohol, at least one non-silicone oil and at least one surfactant, use and process using the composition |
WO2023247574A1 (en) | 2022-06-20 | 2023-12-28 | L'oreal | Composition comprising at least one glycolipid, at least one linear or branched liquid fatty alcohol and at least two polysaccharides, use and process using the composition |
FR3136964A1 (en) | 2022-06-28 | 2023-12-29 | L'oreal | Emulsion with a dialkyl carbonate, coconut oil esters, a volatile hydrocarbon oil and a fatty acid ester polymer and polyoxyethylenated glycol |
FR3136965A1 (en) | 2022-06-28 | 2023-12-29 | L'oreal | Emulsion with a dialkyl carbonate, coconut oil esters, linear C15-C19 alkanes, a volatile hydrocarbon oil and a polyoxyethylene glycol fatty acid ester polymer |
WO2024003305A1 (en) | 2022-06-30 | 2024-01-04 | L'oreal | Use of a composition comprising an alkyl or alkylene carbonate for removing the colour from previously dyed keratinous hair fibres without damaging the keratinous hair fibres |
WO2024003303A1 (en) | 2022-06-30 | 2024-01-04 | L'oreal | Process for removing the colour from previously dyed keratinous hair fibres |
FR3137294A1 (en) | 2022-06-30 | 2024-01-05 | L'oreal | Hair coloring process comprising the application of a (poly)carbodiimide compound, a silicone acrylic copolymer, a particular alkaline agent and a coloring agent |
WO2024008769A1 (en) | 2022-07-05 | 2024-01-11 | L'oreal | Cosmetic composition comprising a natural resin |
WO2024008771A1 (en) | 2022-07-05 | 2024-01-11 | L'oreal | Cosmetic composition comprising a natural resin |
WO2024008772A1 (en) | 2022-07-05 | 2024-01-11 | L'oreal | Cosmetic composition comprising a natural resin |
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WO2021121882A1 (en) | 2019-12-16 | 2021-06-24 | L'oreal | Hair dyeing process using at least one silicone comprising at least one carboxylic acid anhydride group, at least one amino silicone and at least one pigment and/or direct dye |
FR3104432A1 (en) | 2019-12-17 | 2021-06-18 | L'oreal | AQUEOUS COMPOSITION FOR TREATMENT OF KERATINIC FIBERS CONSISTING OF A VEGETABLE OIL, A HYDROCARBON OIL, A NON-IONIC GLYCEROLOUS SURFACTANT, A POLYSACCHARIDE AND A SOLVENT |
WO2021122412A1 (en) | 2019-12-17 | 2021-06-24 | L'oreal | Aqueous composition for treating keratin fibres, comprising a plant oil, a hydrocarbon-based oil, a glycerolated nonionic surfactant, a polysaccharide and a solvent |
WO2021121860A1 (en) | 2019-12-18 | 2021-06-24 | L'oreal | Cosmetic composition comprising a silicone resin and a particular amino silicone |
FR3104993A1 (en) | 2019-12-18 | 2021-06-25 | L'oreal | Cosmetic composition comprising a silicone resin and a particular amino silicone |
FR3104989A1 (en) | 2019-12-18 | 2021-06-25 | L'oreal | Cosmetic composition comprising a hydrophobic film-forming polymer and a particular amino silicone |
WO2021123670A1 (en) | 2019-12-19 | 2021-06-24 | L V M H Recherche | Ultra long-lasting make-up foundation |
FR3104958A1 (en) | 2019-12-19 | 2021-06-25 | L V M H Recherche | Ultra-long-lasting foundation |
FR3104992A1 (en) | 2019-12-20 | 2021-06-25 | L'oreal | Process for coloring keratin materials using a particular oily dispersion and at least two amino compounds different from each other |
WO2021121677A1 (en) | 2019-12-20 | 2021-06-24 | L'oreal | Retinol-based serum |
FR3104976A1 (en) | 2019-12-20 | 2021-06-25 | L'oreal | Retinol-based composition |
FR3104974A1 (en) | 2019-12-20 | 2021-06-25 | L'oreal | Retinol based serum |
FR3104980A1 (en) | 2019-12-20 | 2021-06-25 | L'oreal | A composition comprising a dispersion of polymer particles in a non-aqueous medium, a cationic polymer and an anionic polymer |
FR3104962A1 (en) | 2019-12-20 | 2021-06-25 | L'oreal | Cosmetic composition comprising at least one polar oil, an aliphatic monoalcohol, a mixture of polyols and at least one hydrophilic active agent |
WO2021123352A1 (en) | 2019-12-20 | 2021-06-24 | L'oreal | Retinol-based serum |
FR3104977A1 (en) | 2019-12-20 | 2021-06-25 | L'oreal | Retinol based serum |
WO2021123233A1 (en) | 2019-12-20 | 2021-06-24 | L'oreal | Retinol-based composition |
WO2021123309A1 (en) | 2019-12-20 | 2021-06-24 | L'oreal | Composition comprising a dispersion of polymer particles in a non-aqueous medium, a cationic polymer and an anionic polymer |
WO2021123337A1 (en) | 2019-12-20 | 2021-06-24 | L'oreal | Retinol-based composition |
WO2021123345A1 (en) | 2019-12-20 | 2021-06-24 | L'oreal | Process for colouring keratin materials using a particular oily dispersion and at least two amine compounds that are different from each other |
FR3104957A1 (en) | 2019-12-20 | 2021-06-25 | L'oreal | Composition comprising at least 5% by weight of titanium oxides, an alpha-cyanodiphenylacrylate derivative and a 4-hydroxybenzylidene-malonate or 4-hydroxy-cinnamate derivative |
WO2021123170A1 (en) | 2019-12-20 | 2021-06-24 | L'oreal | Cosmetic composition comprising at least one polar oil, an aliphatic monoalcohol, a mixture of polyols and at least one hydrophilic active agent |
WO2021122039A1 (en) | 2019-12-20 | 2021-06-24 | L'oreal | Composition comprising at least 5% by weight of titanium oxides, an a-cyanodiphenylacrylate derivative and a 4-hydroxybenzylidenemalonate or 4-hydroxycinnamate derivative |
WO2021130335A1 (en) | 2019-12-23 | 2021-07-01 | L'oreal | Emulsified lip gel |
FR3104990A1 (en) | 2019-12-23 | 2021-06-25 | L'oreal | Emulsified lip gel |
WO2021130192A1 (en) | 2019-12-26 | 2021-07-01 | L'oreal | Composition comprising ascorbic acid |
FR3105735A1 (en) | 2019-12-26 | 2021-07-02 | L'oreal | Composition comprising ascorbic acid |
DE102019135833A1 (en) * | 2019-12-27 | 2021-07-01 | Henkel Ag & Co. Kgaa | Antiperspirant cosmetic without cyclic silicone oils |
WO2021167805A1 (en) | 2020-02-19 | 2021-08-26 | L'oreal | Two-step reactive lip system |
FR3108257A1 (en) | 2020-03-20 | 2021-09-24 | L'oreal | TWO-STEP REACTIVE LIP SYSTEM |
FR3108256A1 (en) | 2020-03-23 | 2021-09-24 | L'oreal | REACTIVE TWO-STEP LIP SYSTEM |
WO2021191548A1 (en) | 2020-03-23 | 2021-09-30 | Roquette Freres | Emulsifying and texturing composition based on starches and gums, for cosmetics |
WO2021202156A1 (en) | 2020-03-31 | 2021-10-07 | L'oreal | Mattifying nail compositions |
FR3109313A1 (en) | 2020-04-15 | 2021-10-22 | L'oréal | PROCESS FOR TREATMENT OF KERATINIC MATERIALS USING AN ACRYLIC ANHYDRIDE POLYMER IN OILY DISPERSION AND A HYDROXYL AND / OR THIOLE COMPOUND |
FR3109304A1 (en) | 2020-04-21 | 2021-10-22 | L'oreal | PROCESS FOR DENSIFICATION OF KERATINIC FIBERS BASED ON ACRYLIC SILICONE COPOLYMER AND A COLORING AGENT |
WO2021219722A1 (en) | 2020-04-30 | 2021-11-04 | L'oreal | Aerosol device containing a composition comprising at least one silicone acrylic copolymer and at least one propellant |
FR3109730A1 (en) | 2020-04-30 | 2021-11-05 | L'oreal | Aerosol device containing a composition comprising at least one silicone acrylic copolymer and at least one propellant |
FR3109882A1 (en) | 2020-05-06 | 2021-11-12 | L'oreal | Mattifying compositions for nails |
FR3110840A1 (en) | 2020-05-29 | 2021-12-03 | L'oreal | COMPOSITION FOR TAKING CARE OF AND / OR MAKE-UP OF KERATIN-BASED MATERIALS |
FR3111074A1 (en) | 2020-06-08 | 2021-12-10 | L'oreal | Retinol-based composition |
FR3111075A1 (en) | 2020-06-08 | 2021-12-10 | L'oreal | Retinol-based composition |
WO2021250001A1 (en) | 2020-06-08 | 2021-12-16 | L'oreal | Retinol-based composition |
WO2021250008A1 (en) | 2020-06-08 | 2021-12-16 | L'oreal | Retinol-based composition |
FR3111556A1 (en) | 2020-06-18 | 2021-12-24 | L'oreal | Composition comprising polymer particles, a volatile hydrocarbon-based oil, a film-forming silicone vinyl polymer, a coconut oil |
WO2021260062A1 (en) | 2020-06-23 | 2021-12-30 | L'oreal | Process for treating keratin fibres, comprising the application of a makeup-removing composition, the keratin fibres having been dyed beforehand |
WO2021260048A1 (en) | 2020-06-23 | 2021-12-30 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer comprising at least two different polymer units bearing a(n) (un)saturated hydrocarbon-based chain in a fatty medium |
FR3111557A1 (en) | 2020-06-23 | 2021-12-24 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer comprising at least two different polymer units with a (un) saturated hydrocarbon chain in a fatty medium |
FR3111558A1 (en) | 2020-06-23 | 2021-12-24 | L'oreal | Process for treating keratin fibers comprising the application of a makeup removing composition, the keratin fibers having been previously colored |
WO2021260079A1 (en) | 2020-06-24 | 2021-12-30 | L'oreal | Cosmetic composition comprising a grafted polyhydroxyalkanoate copolymer in a fatty medium |
WO2021260078A1 (en) | 2020-06-24 | 2021-12-30 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer bearing a(n) (un)saturated hydrocarbon-based chain and a surfactant |
FR3111812A1 (en) | 2020-06-24 | 2021-12-31 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer grafted in a fatty medium |
FR3111811A1 (en) | 2020-06-24 | 2021-12-31 | L'oreal | Cosmetic composition comprising a polyhydroxyalkanoate copolymer containing an (un) saturated hydrocarbon chain, and a surfactant |
WO2022002978A1 (en) | 2020-06-30 | 2022-01-06 | L'oreal | Composition comprising a combination of polyglycerol esters |
FR3111810A1 (en) | 2020-06-30 | 2021-12-31 | L'oreal | Composition comprising a combination of fillers |
WO2022002922A1 (en) | 2020-06-30 | 2022-01-06 | L'oreal | Dyeing and/or lightening composition comprising an anthraquinone cationic direct dye, a fatty substance, a chemical oxidizing agent and a basifying agent and/or an oxidation dye precursor |
FR3111799A1 (en) | 2020-06-30 | 2021-12-31 | L'oreal | Composition comprising a combination of polyglycerol esters |
FR3111801A1 (en) | 2020-06-30 | 2021-12-31 | L'oreal | Coloring and / or lightening composition comprising an anthraquinone cationic direct dye, a fatty substance, a chemical oxidizing agent and an alkaline agent and / or an oxidation dye precursor |
WO2022003000A1 (en) | 2020-07-01 | 2022-01-06 | L'oreal | Two-phase composition comprising an alkylpolyglycoside surfactant, a particular diol and an alkane, ester or ether compound comprising from 15 to 30 carbon atoms |
FR3112076A1 (en) | 2020-07-01 | 2022-01-07 | L'oreal | Two-phase composition comprising an alkylpolyglycoside surfactant, a particular diol and an alkane, ester or ether compound comprising from 15 to 30 carbon atoms |
FR3112286A1 (en) | 2020-07-10 | 2022-01-14 | L'oreal | Water-in-oil emulsion with a high aqueous internal phase content |
WO2022008691A1 (en) | 2020-07-10 | 2022-01-13 | L'oreal | Water-in-oil emulsion having a high internal water phase content |
FR3115457A1 (en) | 2020-10-23 | 2022-04-29 | L'oreal | Photoprotective composition |
WO2022084458A1 (en) | 2020-10-23 | 2022-04-28 | L'oreal | Photoprotective composition |
FR3117032A1 (en) | 2020-12-08 | 2022-06-10 | L'oreal | Gel composition comprising silica airgel and ethylguar as thickening agents |
FR3117366A1 (en) | 2020-12-14 | 2022-06-17 | L'oreal | Cosmetic composition comprising at least one hydrocarbon oil and from 4% to 15% by weight of at least one wax chosen from Candelilla wax, Carnauba wax and mixtures thereof |
FR3117850A1 (en) | 2020-12-17 | 2022-06-24 | L'oreal | Process for dyeing keratin fibers using two distinct compounds capable of forming covalent bonds together and a metal salt belonging to the rare earth group |
FR3117849A1 (en) | 2020-12-17 | 2022-06-24 | L'oreal | Process for dyeing keratinous fibers using two distinct compounds capable of forming covalent bonds together as well as a particular metal salt |
FR3117851A1 (en) | 2020-12-17 | 2022-06-24 | L'oreal | Process for dyeing keratin fibers using two distinct compounds capable of forming covalent bonds together as well as a particular organometallic compound |
WO2022128901A1 (en) | 2020-12-17 | 2022-06-23 | L'oreal | Process for dyeing keratin fibres using two different compounds that are capable of forming covalent bonds together and also a particular metal salt or a salt of a metal belonging to the rare-earth metal group or a particular organometallic compound |
WO2022128544A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Cosmetic composition comprising an oily dispersion of polymer particles and an aqueous dispersion of colloidal silica particles |
WO2022129039A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Cosmetic composition comprising a merocyanine, a triazine uv-screening agent, and a polysaccharide modified with hydrophobic chains |
WO2022129477A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Composition comprising aqueous gelling agents, a surfactant, oils, fillers and ascorbic acid |
WO2022129192A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Dispersion comprising a polymeric particle, a stabilizer bearing a c9-c22 alkyl group, an oil and water, and process for treating keratin materials using the dispersion |
FR3117803A1 (en) | 2020-12-18 | 2022-06-24 | L'oreal | Composition comprising aqueous gelling agents, surfactant and ascorbic acid |
WO2022129403A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Composition comprising aqueous gelling agents, surfactants and ascorbic acid |
WO2022129195A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Dispersion comprising a polymeric particle, a stabilizer bearing a c3-c12 cycloalkyl group, an oil and water, and process for treating keratin materials using the dispersion |
WO2022129059A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Cosmetic or dermatological composition comprising a merocyanine and an oily phase comprising at least one citric acid ester |
FR3117785A1 (en) | 2020-12-18 | 2022-06-24 | L'oreal | Cosmetic composition comprising an oily dispersion of polymer particles and an aqueous microdispersion of wax particles. |
WO2022129469A1 (en) | 2020-12-18 | 2022-06-23 | L'oreal | Composition comprising aqueous gelling agents, a surfactant and ascorbic acid |
FR3117786A1 (en) | 2020-12-18 | 2022-06-24 | L'oreal | DISPERSION COMPRISING A POLYMERIC PARTICLE, A STABILIZING AGENT WITH A C3-C12 CYCLOALKYL GROUP, AN OIL AND WATER, PROCESS FOR THE TREATMENT OF KERATIN MATERIALS USING THE DISPERSION |
FR3117798A1 (en) | 2020-12-18 | 2022-06-24 | L'oreal | Cosmetic composition an oily dispersion of polymer particles and an aqueous dispersion of film-forming polymer particles not derived from styrenic monomer. |
FR3117824A1 (en) | 2020-12-18 | 2022-06-24 | L'oreal | Cosmetic or dermatological composition comprising a merocyanine and an oily phase comprising at least one citric acid ester |
FR3117825A1 (en) | 2020-12-18 | 2022-06-24 | L'oreal | Cosmetic or dermatological composition comprising a merocyanine, a triazine UV filter, and a polysaccharide modified by hydrophobic chains |
FR3117847A1 (en) | 2020-12-18 | 2022-06-24 | L'oreal | Composition comprising aqueous gelling agents, surfactants and ascorbic acid |
FR3117793A1 (en) | 2020-12-18 | 2022-06-24 | L'oreal | Cosmetic composition comprising an oily dispersion of polymer particles and an aqueous dispersion of colloidal silica particles |
FR3117799A1 (en) | 2020-12-18 | 2022-06-24 | L'oreal | Composition comprising aqueous gelling agents, surfactant, oils, fillers and ascorbic acid |
FR3117846A1 (en) | 2020-12-18 | 2022-06-24 | L'oreal | DISPERSION COMPRISING A POLYMERIC PARTICLE, A STABILIZING AGENT WITH A C9-C22 ALKYL GROUP, AN OIL AND WATER, PROCESS FOR THE TREATMENT OF KERATIN MATERIALS USING THE DISPERSION |
FR3117862A1 (en) | 2020-12-22 | 2022-06-24 | L'oreal | COMPOSITION FOR THE CARE AND/OR MAKEUP OF KERATINOUS MATERIALS |
FR3117797A1 (en) | 2020-12-22 | 2022-06-24 | L'oreal | Anhydrous deodorant oily composition with dry and fresh effect sprayable without propellant gas |
WO2022136519A1 (en) | 2020-12-22 | 2022-06-30 | L'oreal | Cosmetic composition comprising at least one clay, at least one crystallizable fatty compound and at least one liposoluble uv filter |
FR3117789A1 (en) | 2020-12-22 | 2022-06-24 | L'oreal | Cosmetic composition comprising at least one clay, at least one crystallizable fatty substance and at least one fat-soluble UV filter |
FR3117867A1 (en) | 2020-12-22 | 2022-06-24 | L'oreal | Natural wax microdispersion |
FR3117787A1 (en) | 2020-12-22 | 2022-06-24 | L'oreal | Gelled aqueous composition comprising a heavy grade magnesium salt |
WO2022136441A1 (en) | 2020-12-22 | 2022-06-30 | L'oreal | Gelled aqueous composition comprising a heavy-grade magnesium salt |
FR3117796A1 (en) | 2020-12-22 | 2022-06-24 | L'oreal | Gelled aqueous composition comprising a magnesium salt |
WO2022136439A1 (en) | 2020-12-22 | 2022-06-30 | L'oreal | Gelled aqueous composition comprising a magnesium salt |
FR3117852A1 (en) | 2020-12-23 | 2022-06-24 | L'oréal | Cosmetic composition comprising a copolymer based on acetoacetate functions |
FR3117855A1 (en) | 2020-12-23 | 2022-06-24 | L'oreal | : Cosmetic composition comprising a copolymer based on acetoacetate functions |
WO2022136114A1 (en) | 2020-12-23 | 2022-06-30 | L'oreal | Aqueous dispersion of a specific copolymer, and cosmetic uses thereof |
WO2022136104A1 (en) | 2020-12-23 | 2022-06-30 | L'oreal | Cosmetic composition comprising a copolymer based on acetoacetate functions |
FR3117788A1 (en) | 2020-12-23 | 2022-06-24 | L'oreal | Aqueous dispersion of a specific copolymer and its cosmetic applications |
FR3117854A1 (en) | 2020-12-23 | 2022-06-24 | L'oréal | Cosmetic composition comprising polymeric particles based on acetoacetate functions |
WO2022136110A1 (en) | 2020-12-23 | 2022-06-30 | L'oreal | Cosmetic composition comprising polymer particles based on acetoacetate functions |
FR3117856A1 (en) | 2020-12-23 | 2022-06-24 | L'oréal | Cosmetic composition comprising a block copolymer based on acetoacetate functions |
FR3117853A1 (en) | 2020-12-23 | 2022-06-24 | L'oreal | Cosmetic composition comprising polymeric particles based on acetoacetate functions |
FR3117794A1 (en) | 2020-12-23 | 2022-06-24 | L'oreal | Aqueous dispersion of a specific copolymer and its cosmetic applications |
FR3118701A1 (en) | 2021-01-12 | 2022-07-15 | L'oreal | BIPHASIC COMPOSITION FOR CLEANSING AND/OR MAKE-UP REMOVAL OF KERATINOUS MATERIALS |
FR3118706A1 (en) | 2021-01-12 | 2022-07-15 | L'oreal | BIPHASIC COMPOSITION FOR CLEANSING AND/OR MAKE-UP REMOVAL OF KERATINOUS MATERIALS |
WO2022180010A2 (en) | 2021-02-25 | 2022-09-01 | L'oreal | Composition comprising an organic uv-screening agent, a superabsorbant polymer, perlite and a fatty alcohol |
FR3119988A1 (en) | 2021-02-25 | 2022-08-26 | L'oreal | Aqueous composition comprising an organic UV filter, a superabsorbent polymer, perlite and a fatty alcohol |
WO2022189575A1 (en) | 2021-03-10 | 2022-09-15 | L'oreal | Process for colouring hair keratin fibers comprising the application of a composition comprising at least one (poly)carbodiimide compound and a composition comprising at least one associative polymer and a particular compound |
FR3120533A1 (en) | 2021-03-10 | 2022-09-16 | L'oreal | Process for removing the color from hair keratin fibers which have been previously colored with a specific hair coloring composition |
WO2022189572A1 (en) | 2021-03-10 | 2022-09-15 | L'oreal | Process for removing the colour from previously coloured hair keratin fibers |
FR3120528A1 (en) | 2021-03-10 | 2022-09-16 | L'oreal | Method for removing color from previously colored hair keratin fibers |
FR3120529A1 (en) | 2021-03-10 | 2022-09-16 | L'oreal | Hair coloring composition comprising at least one (poly)carbodiimide compound and at least one compound comprising at least one hydroxy function |
FR3120532A1 (en) | 2021-03-10 | 2022-09-16 | L'oreal | Hair coloring composition comprising at least one (poly)carbodiimide compound and at least one non-carboxylic anionic thickening agent |
FR3120530A1 (en) | 2021-03-10 | 2022-09-16 | L'oreal | Hair coloring process comprising the application of a composition comprising at least one (poly)carbodiimide compound and of a composition comprising at least one associative polymer and a particular compound |
WO2022189576A1 (en) | 2021-03-10 | 2022-09-15 | L'oreal | Hair colouring composition comprising at least one (poly)carbodiimide compound and at least one non-carboxylic anionic thickener |
FR3120527A1 (en) | 2021-03-10 | 2022-09-16 | L'oreal | Process for dyeing hair keratin fibers comprising the application of a composition comprising at least one (poly)carbodiimide compound and of a composition comprising at least one associative polymer and a particular compound |
WO2022189573A1 (en) | 2021-03-10 | 2022-09-15 | L'oreal | Hair colouring composition comprising at least one (poly)carbodiimide compound and at least one compound comprising at least one hydroxyl function |
WO2022189571A1 (en) | 2021-03-10 | 2022-09-15 | L'oreal | Process for removing the colour from hair keratin fibers which have been coloured beforehand with a specific hair colouring composition |
WO2022189570A1 (en) | 2021-03-10 | 2022-09-15 | L'oreal | Process for colouring hair keratin fibers, comprising the application of a composition comprising at least one (poly)carbodiimide compound and a composition comprising at least one associative polymer and a particular compound |
FR3122336A1 (en) | 2021-04-30 | 2022-11-04 | L'oreal | anhydrous composition for caring for and/or making up keratin materials |
WO2022258494A1 (en) | 2021-06-07 | 2022-12-15 | L'oreal | Hair dyeing process comprising the application of a (poly)carbodiimide compound, of a polymer bearing a carboxylic group and of a non-silicone fatty substance |
FR3123567A1 (en) | 2021-06-07 | 2022-12-09 | L'oreal | Hair coloring process comprising the application of a (poly)carbodiimide compound, a polymer containing a carboxylic group and a non-silicone fatty substance |
FR3124079A1 (en) | 2021-06-16 | 2022-12-23 | L'oreal | Composition comprising an oily dispersion of polymer particles, a cationic polymer and an anionic polymer |
WO2022263603A1 (en) | 2021-06-16 | 2022-12-22 | L'oreal | Composition comprising an oily dispersion of polymer particles, a cationic polymer and an anionic polymer |
FR3124081A1 (en) | 2021-06-21 | 2022-12-23 | L'oreal | Cosmetic composition comprising at least one polar oil, one polyol and at least one hydrophilic active |
WO2022268806A1 (en) | 2021-06-21 | 2022-12-29 | L'oreal | Cosmetic composition comprising at least one polar oil, a polyol and at least one hydrophilic active agent |
FR3124698A1 (en) | 2021-06-30 | 2023-01-06 | L'oreal | Composition comprising at least one UV screening agent, boron nitride, and a nonionic surfactant of ester type |
WO2023036686A1 (en) | 2021-09-10 | 2023-03-16 | L'oreal | Makeup kit comprising an aqueous makeup composition and a continuous oily-phase fixing composition with a hydrophobic film-forming polymer |
FR3126875A1 (en) | 2021-09-10 | 2023-03-17 | L'oreal | Make-up kit comprising an aqueous make-up composition, and a fixing composition with a continuous oily phase with a hydrophobic film-forming polymer |
WO2023052587A1 (en) | 2021-09-30 | 2023-04-06 | L'oreal | Cosmetic composition comprising at least one polar oil, a polyol and ascorbic acid |
FR3127398A1 (en) | 2021-09-30 | 2023-03-31 | L'oreal | Cosmetic composition comprising at least one polar oil, one polyol and ascorbic acid |
FR3127695A1 (en) | 2021-10-05 | 2023-04-07 | L'oreal | OILY DISPERSION COMPRISING A POLYMERIC PARTICLE, A STABILIZING AGENT WITH A C9-C22 ALKYL GROUP, AND A PLASTICIZER METHOD FOR TREATMENT OF KERATIN MATERIALS USING THE OILY DISPERSION |
WO2023057446A1 (en) | 2021-10-05 | 2023-04-13 | L'oreal | Oily dispersion comprising a polymeric particle and a stabilizer bearing a c9-c22 alkyl group and a plasticizer, and process for treating keratin materials using the oily dispersion |
FR3129596A1 (en) | 2021-12-01 | 2023-06-02 | L'oreal | Process for dyeing keratinous fibers using a compound bearing a reactive chemical function, an alkoxysilane, a coloring agent and optionally a compound chosen from metal salts, metal compounds belonging to the group of rare earths and metal alkoxides |
FR3129597A1 (en) | 2021-12-01 | 2023-06-02 | L'oreal | Process for treating keratin fibers using an acrylate functionalized polymer and an alkoxysilane |
FR3129832A1 (en) | 2021-12-06 | 2023-06-09 | L'oreal | Non-silicone inverse emulsion comprising a C3 or C4 alkanediol, glycerin, a non-volatile vegetable oil, a polyglyceryl polyricinoleate surfactant and a volatile alkane |
WO2023104475A1 (en) | 2021-12-06 | 2023-06-15 | L'oreal | Silicone-free inverse emulsion comprising a c3 or c4 alkanediol, glycerol, a nonvolatile vegetable oil, a polyglyceryl polyricinoleate surfactant and a volatile alkane |
WO2023104730A1 (en) | 2021-12-09 | 2023-06-15 | L'oreal | Dispersion comprising a polymeric particle, a stabilizer bearing a cycloalkyl group, an oil and water, and process for treating keratin materials using the dispersion |
WO2023104727A1 (en) | 2021-12-09 | 2023-06-15 | L'oreal | Dispersion comprising a polymeric particle, a stabilizer bearing a cycloalkyl group, an oil and a polyol, and process for treating keratin materials using the dispersion |
FR3130131A1 (en) | 2021-12-09 | 2023-06-16 | L'oreal | DISPERSION COMPRISING A POLYMERIC PARTICLE, A STABILIZING AGENT WITH A CYCLOALKYL GROUP, AN OIL, AND A POLYOL, PROCESS FOR THE TREATMENT OF KERATIN MATERIALS USING THE DISPERSION |
FR3130132A1 (en) | 2021-12-09 | 2023-06-16 | L'oreal | DISPERSION COMPRISING A POLYMERIC PARTICLE, A STABILIZING AGENT WITH A CYCLOALKYL GROUP, AN OIL, AND WATER, PROCESS FOR THE TREATMENT OF KERATIN MATERIALS USING THE DISPERSION |
FR3130133A1 (en) | 2021-12-09 | 2023-06-16 | L'oreal | Composition comprising a combination of polyglycerol esters and a filler |
WO2023104924A1 (en) | 2021-12-09 | 2023-06-15 | L'oreal | Composition comprising a combination of polyglycerol esters and a filler |
WO2023107199A1 (en) | 2021-12-09 | 2023-06-15 | L'oreal | Skin perfecting cosmetic compositions and methods of use |
WO2023110424A1 (en) | 2021-12-14 | 2023-06-22 | L'oreal | Cosmetic composition comprising a bis-amino silicone, a cationic surfactant, a fatty alcohol and a fatty alcohol ester, cosmetic treatment process and use |
FR3130158A1 (en) | 2021-12-14 | 2023-06-16 | L'oreal | Cosmetic composition comprising a bis-amino silicone, a cationic surfactant, a fatty alcohol and a fatty alkane, cosmetic treatment method and use |
FR3130159A1 (en) | 2021-12-14 | 2023-06-16 | L'oreal | Cosmetic composition comprising a bis-amino silicone, a cationic surfactant, a fatty alcohol and a fatty alcohol ester, cosmetic treatment method and use |
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WO2023110772A1 (en) | 2021-12-17 | 2023-06-22 | L'oreal | Cosmetic or dermatological composition comprising at least a merocyanine and a hydrotrope |
FR3130573A1 (en) | 2021-12-17 | 2023-06-23 | L'oreal | COSMETIC COMPOSITION COMPRISING A PATTERNED ALKYL-AZLACTONE COPOLYMER AND USES THEREOF |
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FR3130593A1 (en) | 2021-12-17 | 2023-06-23 | L'oreal | Cosmetic or dermatological composition comprising a merocyanine and dipropylene glycol |
FR3130595A1 (en) | 2021-12-17 | 2023-06-23 | L'oreal | Cosmetic or dermatological composition comprising at least one merocyanine and one hydrotrope |
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FR3133311A1 (en) | 2022-03-10 | 2023-09-15 | L'oreal | COMPOSITION COMPRISING AT LEAST ONE AMPS® COPOLYMER, AT LEAST ONE ALKYLPOLYGLUCOSIDE, AT LEAST ONE UV FILTER AND ISOPROPYL MYRISTATE |
WO2023180256A1 (en) | 2022-03-22 | 2023-09-28 | L'oreal | Composition comprising ethyl cellulose, a monoalcohol, a volatile hydrocarbon-based oil, a non-volatile alkane oil, a mono- or di-ester of a fatty acid and of polyglycerol and an ester oil |
FR3133754A1 (en) | 2022-03-22 | 2023-09-29 | L'oreal | Composition comprising ethyl cellulose, a mono-alcohol, a volatile hydrocarbon oil, a non-volatile alkane oil, a mono- or diester of fatty acid and polyglycerol and an alkyl benzoate |
FR3133753A1 (en) | 2022-03-22 | 2023-09-29 | L'oreal | Composition comprising ethyl cellulose, a mono-alcohol, a volatile hydrocarbon oil, a non-volatile alkane oil, a mono- or diester of fatty acid and polyglycerol and a dialkyl carbonate |
FR3133752A1 (en) | 2022-03-22 | 2023-09-29 | L'oreal | Composition comprising ethyl cellulose, a mono-alcohol, a volatile hydrocarbon oil, a non-volatile alkane, a polyglycerol fatty acid ester and a linoleic or oleic acid ester |
FR3133751A1 (en) | 2022-03-22 | 2023-09-29 | L'oreal | Composition comprising ethyl cellulose, a mono-alcohol, a volatile hydrocarbon oil, a non-volatile alkane oil, a mono- or di-ester of fatty acid and polyglycerol and an ester oil |
WO2023194239A1 (en) | 2022-04-08 | 2023-10-12 | L'oreal | Inverse emulsion comprising a dextrin ester, a volatile linear alkane, a natural wax, a natural hydrophilic polymeric gelling agent, and a non-ionic emulsifier |
FR3134315A1 (en) | 2022-04-08 | 2023-10-13 | L'oreal | Inverse emulsion comprising a dedextrin ester, a volatile linear alkane, a natural wax, a natural hydrophilic polymer gelling agent, a non-ionic emulsifier |
FR3134516A1 (en) | 2022-04-15 | 2023-10-20 | L'oreal | Direct emulsion comprising a UV filter, a lipophilic acrylic polymer, a polyol fatty acid ester and an amino acid derivative |
WO2023198923A1 (en) | 2022-04-15 | 2023-10-19 | L'oreal | Direct emulsion comprising a uv-screening agent, a lipophilic acrylic polymer, a fatty acid ester of a polyol and a carboxylic anionic surfactant |
WO2023203036A1 (en) | 2022-04-19 | 2023-10-26 | L'oreal | Inverse emulsion for caring for the skin |
FR3134517A1 (en) | 2022-04-19 | 2023-10-20 | L'oreal | Reverse emulsion for skin care |
WO2023208677A1 (en) | 2022-04-28 | 2023-11-02 | L'oreal | Inverse emulsion comprising a polyphenol, a non-ionic polysaccharide, a polyglycerolated non-ionic surfactant with an hlb ≤ 8, a polyol, a non-volatile plant oil, and a volatile alkane |
FR3134992A1 (en) | 2022-04-28 | 2023-11-03 | L'oreal | Inverse emulsion comprising a polyphenol, a non-ionic polysaccharide, a non-ionic polyglycerol surfactant with HLB ≤ 8, a polyol, a non-volatile vegetable oil, and a volatile alkane |
WO2023230311A1 (en) | 2022-05-27 | 2023-11-30 | L'oréal | Adhesive mascara compositions |
FR3136369A1 (en) | 2022-06-08 | 2023-12-15 | L'oreal | EYEBROW PRIMER |
WO2023247575A1 (en) | 2022-06-20 | 2023-12-28 | L'oreal | Composition comprising at least one glycolipid, at least one linear or branched liquid fatty alcohol, at least one non-silicone oil and at least one surfactant, use and process using the composition |
WO2023247574A1 (en) | 2022-06-20 | 2023-12-28 | L'oreal | Composition comprising at least one glycolipid, at least one linear or branched liquid fatty alcohol and at least two polysaccharides, use and process using the composition |
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WO2024002744A1 (en) | 2022-06-28 | 2024-01-04 | L'oreal | Emulsion with a dialkyl carbonate, coconut oil esters, a volatile hydrocarbon-based oil and a polyethylene glycol dipolyhydroxystearate containing 30 mol of ethylene oxide |
FR3136965A1 (en) | 2022-06-28 | 2023-12-29 | L'oreal | Emulsion with a dialkyl carbonate, coconut oil esters, linear C15-C19 alkanes, a volatile hydrocarbon oil and a polyoxyethylene glycol fatty acid ester polymer |
WO2024003305A1 (en) | 2022-06-30 | 2024-01-04 | L'oreal | Use of a composition comprising an alkyl or alkylene carbonate for removing the colour from previously dyed keratinous hair fibres without damaging the keratinous hair fibres |
WO2024003303A1 (en) | 2022-06-30 | 2024-01-04 | L'oreal | Process for removing the colour from previously dyed keratinous hair fibres |
FR3137285A1 (en) | 2022-06-30 | 2024-01-05 | L'oreal | Process for removing color from previously colored keratin hair fibers |
FR3137283A1 (en) | 2022-06-30 | 2024-01-05 | L'oreal | Use of a composition comprising an alkyl or alkylene carbonate for removing color from previously colored keratin hair fibers without damaging the keratin hair fibers |
FR3137294A1 (en) | 2022-06-30 | 2024-01-05 | L'oreal | Hair coloring process comprising the application of a (poly)carbodiimide compound, a silicone acrylic copolymer, a particular alkaline agent and a coloring agent |
WO2024008771A1 (en) | 2022-07-05 | 2024-01-11 | L'oreal | Cosmetic composition comprising a natural resin |
WO2024008772A1 (en) | 2022-07-05 | 2024-01-11 | L'oreal | Cosmetic composition comprising a natural resin |
FR3137562A1 (en) | 2022-07-05 | 2024-01-12 | L'oreal | Cosmetic composition comprising a natural resin |
FR3137561A1 (en) | 2022-07-05 | 2024-01-12 | L'oreal | Cosmetic composition comprising a natural resin |
FR3137563A1 (en) | 2022-07-05 | 2024-01-12 | L'oreal | Cosmetic composition comprising a natural resin |
WO2024008769A1 (en) | 2022-07-05 | 2024-01-11 | L'oreal | Cosmetic composition comprising a natural resin |
FR3137578A1 (en) | 2022-07-08 | 2024-01-12 | L'oreal | ADHESIVE MASCARA COMPOSITIONS |
FR3137579A1 (en) | 2022-07-08 | 2024-01-12 | L'oreal | ADHESIVE MASCARA COMPOSITIONS |
FR3137831A1 (en) | 2022-07-13 | 2024-01-19 | L'oreal | Oil-in-water emulsion comprising an oily dispersion of polymeric particle stabilized by a C9-C22 alkyl stabilizing agent and a specific plasticizer |
FR3137832A1 (en) | 2022-07-13 | 2024-01-19 | L'oreal | Oil-in-water emulsion comprising a specific polyurethane and filler |
WO2024015451A1 (en) | 2022-07-14 | 2024-01-18 | L'oreal | Vegan semi-solid cosmetic composition |
WO2024023280A1 (en) | 2022-07-29 | 2024-02-01 | L'oreal | Solid anhdrous composition comprising ethylcellulose, an alkyl benzoate and a silicone oil and process employing same |
FR3138312A1 (en) | 2022-07-29 | 2024-02-02 | L'oreal | SOLID ANHYDROUS COMPOSITION COMPRISING ETHYLCELLULOSE, AN ALKYLBENZOATE, A PHENYLATED SILICONE OIL AND METHOD USING SAME |
WO2024049867A1 (en) | 2022-08-31 | 2024-03-07 | L'oreal | Cosmetic compositions with improved wear and transfer resistance |
WO2024047212A1 (en) | 2022-09-02 | 2024-03-07 | L'oreal | Cosmetic composition comprising at least one cationic surfactant, at least one fatty alcohol, at least one glycerol ester and a particular combination of silicones |
FR3139279A1 (en) | 2022-09-02 | 2024-03-08 | L'oreal | Cosmetic composition comprising at least one cationic surfactant, at least one fatty alcohol, at least one glycerol ester and a particular combination of silicones |
FR3139717A1 (en) | 2022-09-19 | 2024-03-22 | L'oreal | ORGANIC SUNSCREEN COMPOSITION AND PROCESS FOR PROTECTING THE SKIN AGAINST PHOTODAMAGE AND AGING |
WO2024077139A1 (en) | 2022-10-05 | 2024-04-11 | L'oreal | Nail composition containing dispersion of acrylic polymer particles |
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ZA200908060B (en) | 2011-04-28 |
WO2008155059A3 (en) | 2009-11-12 |
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