|Numéro de publication||US3439088 A|
|Type de publication||Octroi|
|Date de publication||15 avr. 1969|
|Date de dépôt||16 juin 1964|
|Date de priorité||16 juin 1964|
|Numéro de publication||US 3439088 A, US 3439088A, US-A-3439088, US3439088 A, US3439088A|
|Inventeurs||Edman Walter W|
|Cessionnaire d'origine||Exxon Research Engineering Co|
|Exporter la citation||BiBTeX, EndNote, RefMan|
|Citations de brevets (2), Référencé par (117), Classifications (18)|
|Liens externes: USPTO, Cession USPTO, Espacenet|
United States Patent Ofice 3,439,088 Patented Apr. 15, 1969 Int. Cl. A61k 7/02 US. Cl. 42463 9 Claims ABSTRACT OF THE DISCLOSURE A hydrocarbon solvent having at least 85 wt. percent isoparaffins and having a boiling range of about 360 F. to 428 F. in combination with cosmetic powders and waxes produce a high quality facial cosmetic composition. The function of a hydrocarbon solvent in a cosmetic composition is to aid in the application of powders and waxes to desired areas of the skin. The solvent then evaporates leaving the cosmetic ingredients on the face in the desired amounts. Heretofore, solvents used for this pur pose had unwanted odors and did not evaporate in a reasonable length of time. The solvent of this invention is superior to those previously known in that it is odorless, non-iritating and evaporates quickly upon application.
The present invention is concerned with high quality cosmetic compositions and is particularly concerned with the use of particular hydrocarbon solvents for the preparation of these cosmetic compositions. The invention is particularly concerned with facial cosmetic formulations which contain a major quantity of a hydrocarbon solvent having a very high concentration of isoparafiinic constituents. The solvent used in accordance with the present invention is characterized by being completely odorless, non-irritant and non-greasy, and by having a gradual rate of evaporation. These properties make it eminently hypoallergenic and advantageous in cosmetics for application on live skin.
It is well known in the art to prepare various cosmetic compositions using various types of solvents. Some of these solvents function to aid the application of the desired constituents and then evaporate, leaving the desired active ingredient on the hair or face, as the case may be. One difficulty of the solvents hitherto used is that many of them are not odorless, which detracts from their use. Or if they are odorless, they do not evaporate in a reasonable time. The highly isoparafiinic solvent of the present invention has a relatively narrow and critical boiling range and is highly purified, which renders it particularly adapted for cosmetic formulations.
It has now also been discovered that if a highly refined and highly isoparafiinic solvent be used having a particular boiling range, unexpected desirable results are secured. The solvent is of the type which has at least 85% isoparaffins, preferably in excess of 95%, and most preferably at least 99% by weight of isoparafiins. The preferred compositions are those isoparafiinic hydrocarbon corn positions wherein the contents of unsaturated hydrocarbons, such as aromatics and olefins are less than about 1%, and more preferably less than 0.1% by weight and the contents of cyclo and normal paraffins are less than 10%, and preferably less than about by weight. The preferred compositions are those wherein the total concentrations of non-hydrocarbon impurities such as peroxides, acids, carbonyls, alcohols or other oxygenated compounds are present below about 0.01% by weight, and preferably below 0.001% by weight. In ultimate analysis, the contents of all other elements, particularly S, N and Cl. must be less than 0.0005 by weight.
These highly isoparaffinic compositions may be secured by distilling an alkylate, which is made by reaction between isobutane and an olefin of 3 to 5 carbon atoms, to secure the desired boiling range. The desired cut may be hydrofined and then treated with caustic and adsorbents such as silica gel, alumina, activated char or zeolite to secure the desired purity. These highly isoparaffinic, highly purified fractions may also be secured by the hydrogenation of unsaturated branched olefins of the appropriate boiling range. Isoparaflins constituting this solvent include chiefly tetramethyl hexanes, tetramethyl heptanes and tetramethyl octanes, such as 2,2,4,4-tetramethyl hexane, 2,3,3,5-tetramethyl heptane and 2,2,4,6- tetramethyl octane.
The boiling range of the solvent of the present invention is such that the initial boiling point is higher than about 365 F. and the dry point lower than 428 F., preferably in the range from about 370 to 418 F., and most preferably 374 to 410 F., by ASTM Method D 1078. It is essential that the highly isoparafiinic solvent have an initial boiling point in the range between 360 and 380 F.
The following inspections are typical for this isoparaffinic solvent.
Table I Solvency: Solvent Aniline point, F. (ASTM D-611) 187 Kauri butanol value 26.9 Solubility parameter 1 7.3 Composition, wt. percent:
C isoparaffins 19 C isoparaffins 62 C isoparaffins l9 rr-Paraffins and cycloparafiins 4.6 Aromatics 0.2 Olefins 0.2 Average molecular weight 165 Volatility:
Flash point, F. (ASTM D-56) 144 Vapor pressure 100 F., p.s.i.a. 0.2 Distillation, F. (ASTM D1078):
Initial boiling point 372 5% distilled a-t 374 10% distilled at 375 50% distilled at 379 distilled at 392 distilled at 399 Dry point 406 General:
Specific gravity, 60/60 F. 0.767 Viscosity, centipoise 25 C. 1.541 Refractive index 20 C. 1.4274 Copper corrosion, /2 hr. BP 2 Bromine index (ASTM D-1491) Color, Saybolt +30 Ofiieial Digest of Federation of Societies for Paint Technology, page 726, October 1955.
In the absence of a solute, it tends to evaporate more quickly than mineral spirits of comparable boiling range that are derived from natural petroleum naphtha, as shown by the following data:
TABLE II Minutes elapsed at 25 C. for- Percent evaporated Isoparaflinic Petroleum mineral solvent of 372 to spirits of 361 to 409 F. range 409 F. range ltssurfacetension in air at 25 C. is about 23 dynes/cm,
which is quite low; and its interfacial tension with water at 25 C. is about 49 dynes/cm., which i quite high. These properties make it exceptionally valuable in cosmetic formulations for spreadability. There are no solvents or vehicles available to the cosmetic formulator which have these characteristics. In addition to being odorless and non-irritating, making it safe to use, the viscosity, the non-greasy feel, and the evaporation rate make it particularly distinctive. Other vehicles, such as ethyl and isopropyl alcohol, have a similar viscosity, but evaporate much too quickly for some applications and also have a high odor value. Vehicles such as the fatty acid esters of isopropyl alcohol also have a low odor value and low viscosity, but will never evaporate in any reasonable length of time. In the present invention, these properties confer a distinct advantage to cosmetic face makeup products. They do not leave the skin oily and shiny, but evaporate off leaving the skin with a natural looking matte finish. The solvent evaporates slowly enough so that there is time for the user to be able to evenly distribute the make-up to her face.
The present invention is concerned with a novel cosmetic formulation which, in essence, comprises the highly isoparafiinic solvent described above, a dry powder and a wax. The amount of isoparafiinic solvent present is in the range from about 50-70% by weight, preferably in the range from 55-65% by weight. The amount of dry powder present is in the range from about 15-40% by weight, preferably in the range from about 25-35% by weight. The dry powder is preferably a mixture of talc and titanium dioxide, but other powders, such as zinc oxide, calcium carbonate, kaolin and colloidal silica may be used.
The amount of wax present is in the range from about 4-15% by weight, preferably about 8% by weight. A preferred wax is carnauba wax. Other waxes, such as beeswax, ceresin, ozokerite, microcrystalline wax, parafiin wax, and spermaceti and the like may be used. Other materials may be used in conjunction with the basic composition, such as up to 10% of lanolin, up to 10% of colored pigment or dye and a perfume up to 0.5% by weight.
A number of formulations were prepared having the following compositions:
Table III 'WAX R O U G E Ingredients: Parts by wt. Solvent: Mixed isoparaffins (3704l0 F.) 65.7
Carnauba wax 8.8 Lanolin 4.0 California talc 6.0 Titanium dioxide 12.0 Lake Color, DC Red No. 30 3.0
Perfume, pts. by vol. 0.5
FOUNDATION MAKE-UP d t Formulation In e ients w ercent;
P D E F Solvent:
Mixed isoparaffins (370-410" F.),
solvent X 54. 53. Isopropyl myl'i tote 63.5 Solute:
Carnauba wax 7. 0 5. 0 5. 0 Lanolin 3.0 Beeswax 1.0 1.0 Solids: Dry powder 35. 5 40. 0 40. 0 Perfume 0. 5 0. 5 0. 5
The dry powder contains the following ingredients in wt. percent:
Talc 43.9 Colloidal clay 18.7 Chalk 24.95 Titanium dioxide 9.95 Color mix (blended to desired shade) 2.5
Three comparable formulations, A, B and C, of wax rouge were prepared with 33.8 parts by weight of total solute and 0.5 part by volume of perfume as in the wax rouge shown in Table III, and with 67.5 parts by weight of three different solvents as shown in Table IV.
Formulation C is a standard reference according to the prior art. Formulation B has solvent X replacing the isopropyl myristate of the standard reference. Formulation A has solvent X, isoparafiinic solvent (370-410 F.) as the sole solvent. The three formulations were tested on womens faces.
Formulation C gave the oiliest film, which was objectionably shiny. Formulations B and C rubbed off easily. Formulation A, made in accordance with the present invention, was creamier and therefore applied moreeasily than B or C. Formulation A developed a desirably dul or matte finish and was not easily rubbed off.
In Table III, Formulation F is a standard reference foundation make-up according to the prior art. Formulation E applied as smoothly and as easily as F, but was a little chalkier on the skin. Formulation D, containing no beeswax, was subjected to half-face tests by a fivemember panel of women in direct comparison with three widely advertised commercial brands of make-up. Three of the five panel members preferred FormulationD, because it was not greasy and left a more natural matte finish. The only objection the other two panel members had to Formulation D was that it didnt spread easily; but the fact that it went on sparingly was considered a positive advantage by one of the other three panel members. All five panel members thought it necessary to use powder on the half-faces with the commercial brands of make-up because they were shiny; but none of the five panel members thought it necessary to use powder on the half-faces with Formulation D.
The present invention is a composition of matter suitable for use as a facial cosmetic and comprising a major proportion of a predominantly isoparaffinic hydrocarbon solvent boiling in the range of 360-428 F a minor proportion of 5 to 15% of organic binder selected from the class of waxes and fats, and a minor proportion of 10 to 43% of inorganic powder selected from the class of fillers and pigments.
What is claimed is:
1. Cosmetic composition which comprises in combination from about 50 to by weight of a hydrocarbon solvent, from about 15 to 40% by weight of a powder and 4 to 15% by weight of a wax, said solvent being characterized by boiling in the range from about 360 to 428 F. and being further characterized by having an isoparaffin concentration greater than about by weight.
2. Composition as defined by claim 1 wherein the isoparaffinic content of said solvent is greater than about by weight and wherein the unsaturated content of said solvent is less than about 1% by weight.
3, Composition as defined by claim 1 wherein said powder is selected from the class of fillers and pigments and wherein said wax is a hydrocarbon wax.
4. Composition as defined by claim 1 wherein the isoparafiinic content of said solvent is greater than about 99% by weight, wherein the unsaturated content is below about 0.1% by weight and wherein the initial boiling point of said solvent is in the range from about 360 to 380 F.
5. Composition as defined by claim 3 wherein said powder is selected from the class consisting of talc, colloidal clay, chalk and titanium dioxide.
6. Composition as defined by claim 5 wherein said wax is a carnauba wax.
7. Composition as defined by claim 6 wherein from about 2 to by weight of lanolin is utilized in said composition.
8. The composition as defined by claim 1 wherein the isoparaflinic content of said solvent is greater than about 99% by weight, wherein the unsaturated content is below about 0.1% by weight and wherein the initial boiling point of said solvent is in the range from about 360 to 380 F.; the powder is selected from the class consisting of talc, colloidal clay, chalk and titanium dioxide; and the wax is carnauba wax.
9. A water-free cosmetic composition which comprises in combination from about to by weight of a hydrocarbon solvent, from about 15 to 40% by weight References Cited UNITED STATES PATENTS 3,211,618 10/ 1965 Karnbersky 167-90 FOREIGN PATENTS 1,134,797 8/ 1962 Germany.
OTHER REFERENCES Larson et al., Official Digest, January 1954, pp. 45-48 (photocopy in 167-85), (copy of above in Group Sagarin, Cosmetics Science and Technology, September 1957, PP. 262-270 (p. 263 relied upon), TP 983 S25c. (Copy in Group 120.)
ALBERT T. MEYERS, Primary Examiner.
D. R. MA-HANAND, Assistant Examiner.
U.S. Cl. X.R.
|Brevet cité||Date de dépôt||Date de publication||Déposant||Titre|
|US3211618 *||26 juin 1961||12 oct. 1965||Helene Kambersky||Base for cosmetics|
|DE1134797B *||20 juin 1961||16 août 1962||Helene Kambersky Geb Vierthale||Grundlage fuer Schminke|
|Brevet citant||Date de dépôt||Date de publication||Déposant||Titre|
|US3818105 *||23 août 1971||18 juin 1974||Exxon Research Engineering Co||Composition and process for lubricating the skin|
|US4183898 *||25 mai 1978||15 janv. 1980||Liff Lawrence J||Liquid base makeup composition|
|US4349535 *||11 janv. 1980||14 sept. 1982||Liff Lawrence J||Liquid base makeup composition|
|US4374825 *||17 févr. 1981||22 févr. 1983||The Proctor & Gamble Company||Hair conditioning compositions|
|US4387090 *||13 févr. 1981||7 juin 1983||The Procter & Gamble Company||Hair conditioning compositions|
|US4472375 *||1 oct. 1982||18 sept. 1984||The Procter & Gamble Company||Hair conditioning compositions|
|US5165915 *||14 juin 1990||24 nov. 1992||Shiseido Company Ltd.||Spherical clay mineral powder, process for production thereof and composition containing the same|
|US6541017||24 juin 1999||1 avr. 2003||L'oreal S.A.||Anhydrous composition and cosmetic, pharmaceutical or hygienic use|
|US6589538||24 juin 1999||8 juil. 2003||L'oreal S.A.||Anhydrous composition and cosmetic, pharmaceutical or hygienic use|
|US7214382||5 juin 2003||8 mai 2007||Adi Shefer||Self-warming or self-heating cosmetic and dermatological compositions and method of use|
|US7264821||14 févr. 2003||4 sept. 2007||L'oreal||Anhydrous composition and cosmetic, pharmaceutical or hygienic use|
|US7271209 *||19 févr. 2004||18 sept. 2007||Exxonmobil Chemical Patents Inc.||Fibers and nonwovens from plasticized polyolefin compositions|
|US7531594||19 févr. 2004||12 mai 2009||Exxonmobil Chemical Patents Inc.||Articles from plasticized polyolefin compositions|
|US7619026||12 août 2003||17 nov. 2009||Exxonmobil Chemical Patents Inc.||Plasticized polyolefin compositions|
|US7619027||24 oct. 2006||17 nov. 2009||Exxonmobil Chemical Patents Inc.||Plasticized polyolefin compositions|
|US7622523||9 févr. 2005||24 nov. 2009||Exxonmobil Chemical Patents Inc.||Plasticized polyolefin compositions|
|US7632887||4 août 2003||15 déc. 2009||Exxonmobil Chemical Patents Inc.||Plasticized polyolefin compositions|
|US7652092||19 avr. 2006||26 janv. 2010||Exxonmobil Chemical Patents Inc.||Articles from plasticized thermoplastic polyolefin compositions|
|US7652093||19 avr. 2006||26 janv. 2010||Exxonmobil Chemical Patents Inc.||Plasticized polyolefin compositions|
|US7652094||12 mai 2006||26 janv. 2010||Exxonmobil Chemical Patents Inc.||Plasticized polyolefin compositions|
|US7858701||3 avr. 2008||28 déc. 2010||Exxonmobil Chemical Patents Inc.||Soft homogeneous isotactic polypropylene compositions|
|US7875670||25 févr. 2009||25 janv. 2011||Exxonmobil Chemical Patents Inc.||Articles from plasticized polyolefin compositions|
|US7906588||6 oct. 2008||15 mars 2011||Exxonmobil Chemical Patents Inc.||Soft heterogeneous isotactic polypropylene compositions|
|US7985801||13 sept. 2007||26 juil. 2011||Exxonmobil Chemical Patents Inc.||Fibers and nonwovens from plasticized polyolefin compositions|
|US7998579||29 avr. 2005||16 août 2011||Exxonmobil Chemical Patents Inc.||Polypropylene based fibers and nonwovens|
|US8003725||15 août 2006||23 août 2011||Exxonmobil Chemical Patents Inc.||Plasticized hetero-phase polyolefin blends|
|US8080583||20 déc. 2011||Elc Management Llc||Emulsion cosmetic compositions containing resveratrol derivatives and linear or branched silicone|
|US8084496||6 mai 2010||27 déc. 2011||Elc Management Llc||Resveratrol ferulate compounds and compositions|
|US8084506||20 mars 2009||27 déc. 2011||Mary Kay Inc.||Sebum absorption compositions|
|US8192813||18 juin 2008||5 juin 2012||Exxonmobil Chemical Patents, Inc.||Crosslinked polyethylene articles and processes to produce same|
|US8193155||9 févr. 2009||5 juin 2012||Elc Management, Llc||Method and compositions for treating skin|
|US8211968||25 janv. 2010||3 juil. 2012||Exxonmobil Chemical Patents Inc.||Plasticized polyolefin compositions|
|US8217112||19 oct. 2009||10 juil. 2012||Exxonmobil Chemical Patents Inc.||Plasticized polyolefin compositions|
|US8221731||18 mai 2009||17 juil. 2012||Aveda Corporation||Continuous moisturization compositions|
|US8221732||6 juin 2011||17 juil. 2012||Aveda Corporation||Continuous moisturization compositions|
|US8344024||27 mai 2008||1 janv. 2013||Elc Management Llc||Anhydrous cosmetic compositions containing resveratrol derivatives|
|US8362076||11 nov. 2011||29 janv. 2013||Elc Management Llc||Ascorbic acid esters of resveratrol and cosmetic compositions|
|US8389615||7 juil. 2006||5 mars 2013||Exxonmobil Chemical Patents Inc.||Elastomeric compositions comprising vinylaromatic block copolymer, polypropylene, plastomer, and low molecular weight polyolefin|
|US8394394||12 mars 2013||L'oréal||Mousse formulations|
|US8461200||11 nov. 2011||11 juin 2013||Elc Management Llc||Salicylic acid esters of resveratrol and cosmetic compositions|
|US8465731||12 mars 2010||18 juin 2013||Elc Management, Llc||Probiotic color cosmetic compositions and methods|
|US8491921||6 févr. 2012||23 juil. 2013||Elc Management, Llc||Compositions and methods for tinting keratin material|
|US8506974 *||12 nov. 2008||13 août 2013||Presperse Corporation||Silicon-free hydrocarbons providing aesthetic volatility|
|US8506975 *||9 déc. 2009||13 août 2013||Presperse Corporation||Cosmetic compositions utilizing a silicone-free hydrocarbon complex|
|US8513347||7 juil. 2006||20 août 2013||Exxonmobil Chemical Patents Inc.||Elastomeric compositions|
|US8529923||4 août 2009||10 sept. 2013||Chanel Parfums Beaute||Cosmetic composition based on substantially hemispherical particles|
|US8535738||7 juil. 2008||17 sept. 2013||Elc Management, Llc||Methods and compositions for treating skin|
|US8703030||31 déc. 2010||22 avr. 2014||Exxonmobil Chemical Patents Inc.||Crosslinked polyethylene process|
|US8703161||23 juin 2009||22 avr. 2014||Elc Management, Llc||Skin repair compositions comprising circadian gene activators and a synergistic combination of Sirt1 gene activators|
|US8722026||4 janv. 2011||13 mai 2014||Elc Management, Llc||Skin lightening compositions|
|US8765156||30 avr. 2010||1 juil. 2014||Elc Management Llc||Topical compositions comprising inorganic particulates and an alkoxylated diphenylacrylate compound|
|US8840929||3 déc. 2013||23 sept. 2014||Elc Management Llc||Cosmetic compositions with near infra-red (NIR) light-emitting material and methods therefor|
|US8852616||3 déc. 2013||7 oct. 2014||Elc Management Llc||Cosmetic compositions with near infra-red (NIR) light-emitting material and methods therefor|
|US8956624||21 nov. 2008||17 févr. 2015||Elc Management, Llc||Compositions and methods for treating skin with extract from Trametes|
|US8962571||20 avr. 2012||24 févr. 2015||Elc Management||Method for repairing DNA damage in keratinocytes|
|US8992897||19 oct. 2012||31 mars 2015||Elc Management Llc||Skin lightening compositions|
|US9028849||12 juin 2013||12 mai 2015||Elc Management Llc||Compositions and methods for tinting keratin material|
|US9072717||18 sept. 2007||7 juil. 2015||Elc Management Llc||Cosmetic compositions containing alpha glucosidase inhibitors and methods of use|
|US9095543||28 avr. 2010||4 août 2015||Elc Management Llc||Cosmetic compositions comprising cyanodiphenylacrylates|
|US9162083||16 avr. 2013||20 oct. 2015||Elc Management Llc||Linoleic and Linolenic acid esters of resveratrol and cosmetic compositions|
|US9180316||16 avr. 2013||10 nov. 2015||Elc Management Llc||Butyric acid esters of resveratrol and cosmetic compositions|
|US9220669||7 mai 2010||29 déc. 2015||Elc Management Llc||Resveratrol ferulate compounds, compositions containing the compounds, and methods of using the same|
|US20030143170 *||14 févr. 2003||31 juil. 2003||L'oreal S.A.||Anhydrous composition and cosmetic, pharmaceutical or hygienic use|
|US20040054040 *||4 août 2003||18 mars 2004||Lin Chon Yie||Plasticized polyolefin compositions|
|US20040072000 *||10 juin 2003||15 avr. 2004||Kawka Dariusz Wlodzimierz||Aramid paper laminate|
|US20040106723 *||12 août 2003||3 juin 2004||Yang Henry Wu-Hsiang||Plasticized polyolefin compositions|
|US20040186214 *||19 févr. 2004||23 sept. 2004||Wen Li||Fibers and nonwovens from plasticized polyolefin compositions|
|US20040253198 *||5 juin 2003||16 déc. 2004||Adi Shefer||Self-warming or self-heating cosmetic and dermatological compositions and method of use|
|US20040260001 *||19 févr. 2004||23 déc. 2004||Lin Chon-Yie||Articles from plasticized polyolefin compositions|
|US20050148720 *||9 févr. 2005||7 juil. 2005||Wen Li||Plasticized polyolefin compositions|
|US20060039886 *||25 oct. 2005||23 févr. 2006||Adi Shefer||Self-warming or self-heating cosmetic and dermatological compositions and method of use|
|US20060167184 *||30 déc. 2005||27 juil. 2006||Waddell Walter H||Innerliners for use in tires|
|US20060189744 *||19 avr. 2006||24 août 2006||Tse Mun F||Articles from plasticized thermoplastic polyolefin compositions|
|US20060189763 *||19 avr. 2006||24 août 2006||Yang Henry W||Plasticized polyolefin compositions|
|US20060205863 *||12 mai 2006||14 sept. 2006||Lin Chon Y||Plasticized polyolefin compositions|
|US20070021561 *||7 juil. 2006||25 janv. 2007||Tse Mun F||Elastomeric compositions|
|US20070100053 *||24 oct. 2006||3 mai 2007||Chapman Bryan R||Plasticized polyolefin compositions|
|US20080249231 *||3 avr. 2008||9 oct. 2008||Sudhin Datta||Soft homogeneous isotactic polypropylene compositions|
|US20080317990 *||18 juin 2008||25 déc. 2008||Exxonmobil Chemical Company Inc.||Crosslinked polyethylene articles and processes to produce same|
|US20090035237 *||27 mai 2008||5 févr. 2009||Maes Daniel H||Emulsion Cosmetic Compositions Containing Resveratrol Derivatives And Silicone Surfactant|
|US20090035240 *||27 mai 2008||5 févr. 2009||Maes Daniel H||Aqueous Based Cosmetic Compositions Containing Resveratrol Derivatives And An Aqueous Phase Structuring Agent|
|US20090035242 *||27 mai 2008||5 févr. 2009||Maes Daniel H||Emulsion Cosmetic Compositions Containing Resveratrol Derivatives And Linear Or Branched Silicone|
|US20090035243 *||27 mai 2008||5 févr. 2009||Anna Czarnota||Anhydrous Cosmetic Compositions Containing Resveratrol Derivatives|
|US20090068132 *||4 sept. 2008||12 mars 2009||Daniela Bratescu||Resveratrol Ferulate Compounds, Compositions Containing The Compounds, And Methods Of Using The Same|
|US20090092566 *||9 oct. 2007||9 avr. 2009||Lentini Peter J||Self-tanning cosmetic compositions and methods|
|US20090111946 *||6 oct. 2008||30 avr. 2009||Sudhin Datta||Soft Heterogeneous Isotactic Polypropylene Compositions|
|US20090123398 *||12 nov. 2008||14 mai 2009||Presperse, Inc.||Silicon-free hydrocarbons providing aesthetic volatility|
|US20090196942 *||1 févr. 2008||6 août 2009||Goyarts Earl C||Topical compositions containing citrus jabara extract|
|US20090220481 *||9 févr. 2009||3 sept. 2009||Maes Daniel H||Method and compositions for treating skin|
|US20090247648 *||20 mars 2009||1 oct. 2009||Mary Kay Inc.||Sebum absorption compositions|
|US20090291056 *||20 mai 2008||26 nov. 2009||Castro John R||Aqueous Based Cosmetic Compositions With Clear Or Translucent Non-Amidated Structuring Agent|
|US20090297466 *||18 mai 2009||3 déc. 2009||Erik Gutmann||Continuous Moisturization Compositions|
|US20100015072 *||17 juin 2009||21 janv. 2010||Christopher Polla||Topical Compositions Comprising Isonicotinamide|
|US20100028317 *||23 juin 2009||4 févr. 2010||Maes Daniel H||Skin Repair Compositions Comprising Circadian Gene Activators And A Synergistic Combination Of Sirt1 Gene Activators|
|US20100143426 *||9 déc. 2009||10 juin 2010||Presperse, Inc.||Cosmetic dispersions utilizing a silicone-free hydrocarbon complex|
|US20100203077 *||21 nov. 2008||12 août 2010||Schnittger Steven F||Compositions And Methods For Treating Skin With Extract From Trametes|
|US20100215755 *||26 août 2010||Daniela Bratescu||Resveratrol Ferulate Compounds, Compositions Containing The Compounds, And Methods Of Using The Same|
|US20100216879 *||26 août 2010||Maes Daniel H||Resveratrol Ferulate Compounds And Compositions|
|US20100323042 *||7 juil. 2008||23 déc. 2010||Collins Donald F||Methods And Compositions For Treating Skin|
|US20110021704 *||7 juil. 2006||27 janv. 2011||Tse Mun Fu||Elastomeric compositions comprising vinylaromatic block copolymer, polypropylene, plastomer, and low molecular weight polyolefin|
|US20110044919 *||11 août 2008||24 févr. 2011||Giacomoni Paolo U||Compositions With Perfluorinated Ingredients|
|US20110110988 *||12 mai 2011||Milanka Susak||Topical Compositions Comprising Inorganic Particulates And An Alkoxylated Diphenylacrylate Compound|
|US20110111153 *||31 déc. 2010||12 mai 2011||Exxonmobil Chemical Company Inc.||Crosslinked polyethylene process|
|US20110171149 *||14 juil. 2011||Yoko Niki||Skin Lightening Compositions|
|US20110171288 *||16 janv. 2009||14 juil. 2011||Fatemeh Mohammadi||Topical compositions and methods for whitening skin|
|US20110223219 *||12 mars 2010||15 sept. 2011||Khanh Ngoc Dao||Probiotic Color Cosmetic Compositions And Methods|
|US20110236327 *||29 sept. 2011||Erik Gutmann||Continuous Moisturization Compositions|
|EP0197206A2 *||24 déc. 1985||15 oct. 1986||INTERCOS ITALIA S.p.A.||Article for the presentation of a pasty cosmetic product and the related production process|
|EP0263327A2 *||14 sept. 1987||13 avr. 1988||Webcraft Technologies, Inc.||Advertising sampler and method of manufacture|
|EP0752845A1 *||27 févr. 1995||15 janv. 1997||THE PROCTER & GAMBLE COMPANY||Powder cosmetic compositions|
|EP2083043A1||4 août 2003||29 juil. 2009||ExxonMobil Chemical Patents Inc.||Plasticized polyolefin compositions|
|EP2535360A1||18 déc. 2007||19 déc. 2012||ExxonMobil Research and Engineering Company||Process for fluid phase in-line blending of polymers|
|WO2010027491A1||4 sept. 2009||11 mars 2010||Exxonmobil Research And Engineering Company||Process for feeding ethylene to polymerization reactors|
|WO2010091327A2||8 févr. 2010||12 août 2010||Elc Management Llc||Method and compositions for treating skin|
|WO2012174091A2||13 juin 2012||20 déc. 2012||The Procter & Gamble Company||PERSONAL CARE COMPOSITIONS COMPRISING A pH TUNEABLE GELLANT AND METHODS OF USING|
|WO2012174096A2||13 juin 2012||20 déc. 2012||The Procter & Gamble Company||Personal care compositions comprising a di-amido gellant and methods of using|
|WO2012177757A2||20 juin 2012||27 déc. 2012||The Procter & Gamble Company||Personal care compositions comprising shaped abrasive particles|
|Classification aux États-Unis||424/63|
|Classification internationale||A61Q1/12, A61K8/29, A61K8/31, A61Q1/08, A61K8/30, A61K8/19, A61Q1/02|
|Classification coopérative||A61K8/31, A61Q1/02, A61Q1/12, A61K8/29, A61Q1/08|
|Classification européenne||A61Q1/08, A61K8/31, A61K8/29, A61Q1/02, A61Q1/12|