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Publication numberUS3818105 A
Publication typeGrant
Publication dateJun 18, 1974
Filing dateAug 23, 1971
Priority dateAug 23, 1971
Publication numberUS 3818105 A, US 3818105A, US-A-3818105, US3818105 A, US3818105A
InventorsM Coopersmith, W Kochenderfer, L Felty
Original AssigneeExxon Research Engineering Co
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Composition and process for lubricating the skin
US 3818105 A
Abstract
C12-C14 isoparaffinic hydrocarbon fractions are effective skin lubricants and cosmetic formulation constituents. The paraffinic oils possess a unique combination of properties, namely, low viscosity, moderate volatility, plus the ability to disperse dyes and/or pigments. Typically, the isoparaffinic hydrocarbon fraction makes up less than 50 weight % of the total cosmetic formulation and are normally admixed with water, monoalkanols, alkyl and aryl esters, humectant compositions, surfactants, lanolin, white oils, pigments, dyes, clays, perfumes and mixtures thereof.
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United States Patent [191 Coopersmith et al.

[ June 18, 1974 [73] Assignee: Esso Research and Engineering Company, Linden, NJ.

[22] Filed: vAug. 23, 1971 [21] Appl. No.: 174,231

[52] US. Cl 424/358, 424/63, 424/64, 424/70, 424/73, 424/168, 424/355 [51 Int. Cl. A6lk 7/00, A6ll 23/00 [58] Field of Search 424/358, 70, 73, 63, 64,

[56] References Cited UNITED STATES PATENTS 2,628,205 2/1953 Shoemaker 424/83 3,439,088 4/l969 Edman 3,574,827 4/197] Beerbower 424/358 X OTHER PUBLICATIONS Wells et al., Cos. & The Skin, Reinhold Pub. N.Y., 1964, pp. 654-654.

DeNavarre, The Chem. & Mfg. of Cos., 2nd ed, Vol. II, pp. 359-367.

Primary ExaminerAlbert T. Meyers Assistant ExaminerAnna P. F agelson 57 ABSTRACT C C isoparaffinic hydrocarbon fractions are effective skin lubricants and cosmetic formulation constituents. The paraffinic oils possess a unique combination of properties, namely, low viscosity, moderate volatility, plus the ability to disperse dyes and/or pigments. Typically, the isoparaffinic hydrocarbon fraction makes up less than 50 weight of the total cosmetic formulation and are normally admixed with water, monoalkanols, alkyl and aryl esters, humectant compositions, surfactants, lanolin, white oils, pigments, dyes, clays, perfumes and mixtures thereof.

2 Claims, N0 Drawings BACKGROUND OF THE INVENTION I. Field of the Invention This invention relates to cosmetic formulations and a method for the beneficiation of the human body, in particular the hair, nails and skin of the cosmetic user. More particularly, the invention relates to cosmetic formulations comprising an effective amount of a C C isoparaffinic hydrocarbon fraction and to a process for using the same.

ll. Description of the Prior Art Various types of hydrocarbon materials have been employed as constituents in cosmetic formulations. The most commonly employed hydrocarbon materials are the relatively high molecular weight, high boiling, white mineral oils and petrolatums (see Cosmetics and The Skin by Wells and Labowe,-pp. 654-657 and The Chemistry and Manufacture of Cosmetics, by Maison G. DeNavarre, Volume II, second Edition, pp. 359-367). Mineral oils and petrolatum are used in cosmetic products primarily because of their neutral, stable, and odorless character. These compositions are heavy, viscous materials that are substantially nonvolatile at atmospheric conditions and which do not serve as dispersion media for dyes or pigments in cosmetic preparations. The use of lower molecular weight, more volatile hydrocarbon materials has also been reported in the literature. Specifically, Kambersky in US. Pat. No. 3,21 1,618 reported that paraffms, in particular isoparaffins (branched hydrocarbons) having a boiling range between l60-200C., could be used as a volatile constituent for eyelash and eyebrow cosmetics. Also in US. Pat. No. 2,439,088, the use ofa hydrocarbon solvent for cosmetic preparations is disclosed, specifically C to C isoparaffins having a boiling range of 183 to 222C. are taught as useful in combination with cosmetic powders and waxes.

Such materials, because of their very high volatility, give relatively little duration of feel and cosmetic materials prepared containing the same, 'quickly lose effectiveness, as the hydrocarbon constituents evaporate within a few minutes after application.

SUMMARY OF THE INVENTION In accordance with the present invention, it has been found that C -C isoparafi'lnic fractions composed of branched chain aliphatic and naphthenic materials are highly effective constituents for a wide spectrum of cosmetic formulations and topical pharmaceuticals. The preferred paraffin materials are composed of a major amount, i.e., more than 50 weight of branched, noncyclic, nonsubstituted, aliphatic hydrocarbons having from 12 to 14 carbon atoms and a minor amount, i.e., up to 50 weight of alicyclic, nonsubstituted, naphthenic hydrocarbons. The C C isoparaffinic hydrocarbon fractions are colorless, essentially odorless compositions that possess low viscosity and moderate evaporation properties. The unique combination of volatility and viscosity of these materials permits the skin to be lubricated by a quick spreading, nongreasy oil that evaporates after use and thereby does not permit residual oil buildup. Typically, cosmetic formulations contain less than about 50 wt. of the C -Q, isoparaffinic hydrocarbon fraction and are normally employed in combination with various types of typical cosmetic ingredients.

The isoparaffinic hydrocarbon fractions employed in this invention are obtained by distillation of suitable fractions of motor fuel alkylation bottoms. The C C fraction boiling between about 225 to'255C. are then purified to cosmetic grade quality.

As noted earlier, usable hydrocarbon fractions are C, C,., isoparaffinic hydrocarbon fractions. The expression C C isoparaffinic hydrocarbon fraction as used herein is meant to encompass hydrocarbon compositions composed of a major amount, i.e.,

- greater than 50%, preferably from about 70 to 90%,

most preferably from about to of branched chain, noncyclic, nonsubstituted aliphatic hydrocarbons having from 12 to 14 carbon atoms and a minor amount of alicyclic nonsubstituted, napthenic hydrocarbons. The useful hydrocarbon materials have a distillation range (atmospheric boiling points) varying from about 225 to 225C. as determined by ASTM Method D 86. The properties of a typical C r-C isoparaffinic hydrocarbon fraction are as follows: Specific gravity at 20/20C. of 0.788 as determined by ASTM Method D 1217; a kinematic viscosity of 4.6 centistokes at 20C. as determined by ASTM Method D 445; a SSU viscosity at F. of about 36; a refractive index (n of 1.439 as determined by ASTM Method D 1218; a flash point of F. (COC) as determined by ASTM Method D 56; a pour point of 76F. as determined by ASTM Method D 97; a surface tension of about 25.0 dynes/centimeter at 25C; and an interfacial tension (on water) of about 53.0 dynes/centimeter at 25C.

The isoparaffinic hydrocarbon is used in admixture with one or more additional ingredients to arrive at a final cosmetic formulation. Typically, the isoparaffinic hydrocarbon is used in cosmetic formulations in amounts less than about '50 wt. generally from 0.5 to 50 wt. based on total formulation. The amount of isoparaffinic hydrocarbon employed depends primarily upon the cosmetic type. For example, the isoparaffmic oil may make up only about 5 wt. of liquid make-up compositions whereas concentrations approaching 50 wt. of the isoparaffinic hydrocarbon may be used in spreading bath oils.

The isoparaffinic hydrocarbon is used in cosmetic formulations in admixture with one or more of the following substituents:

1. Water;

2. C -C monoalkanols, e.g., ethanol, isopropanol,

butanol, etc.; I

3. Organic ester dispersion media, e.g., C -C aliphatic and aromatic acid esters of C -C monoalkanols, for example, diisopropyl adipate, isopropyl myristate, butyl stearate, etc.;

4. Humectant compositions, in particular polyhydroxy compounds such as dipropylene glycol, glycerol, polyethylene gylcol, propylene glycol, sorbitan, butanediol, etc.;

5. Lanolin;

6. Clay minerals and inorganic silicates, for example,

kaolin, bentonite, zeolite, talc, Fullers earth, diatomaceous eath, zinc silicate, lithium silicate, etc.;

7. Dyes and metal oxide pigments such as titanium dioxide, zinc oxide, iron oxide, etc.;

8. Surfactant compositions, e.g., (a) sulfonated and sulfated oils such as sulfonated normal glycerides,

sulfated fatty alcohol ethoxylates, sulfated glycol monoesters, sulfonated methyl, ethyl and butyl fatty acid esters, etc.; (b) alkylaryl sulfonates, such as dodecyl benzene sulfonates; c) ammonium, calcium, magnesium, potassium, sodium, zinc and alkanol amine derivatives of sulfated C, C alcohols such as sodium myristyl sufate, sodium lauryl sulfate, etc.; (d) quaternary ammonium compounds such as lauryland stearyldimethylbenzyl ammonium chloride; (e) alkoxylated, in particular, ethoxylated higher fatty alcohols, higher fatty acids, fatty esters, alkylphenols, etc.;

Animal, vegetable and hydrocarbon waxes such as beeswax, carnauba, jojoba, paraffin wax, microcystalline hydrocarbon wax, etc.;

10. White oils and petrolatum', and

l 1. Perfume and fragrance materials.

The isoparaffinic hydrocarbon materials, can of course be used in cosmetic formulations that contain materials other than those specified above. The above listing is intended to indicate that the subject C C isoparaffinic materials can be used in a wide range of cosmetic formulations. For example, the hydrocarbon materials can be used in face make-up, body make-up, eye shadow, mascara, hair coloring, dyeing preparations, lip rouge, cheek rouge, masking preparations, eyebrow preparations, eyeliner, hand cleaners, bath oils, as well as other types of oil and water emulsions, water-in-oil emulsions, alcoholic emulsions, wax and oilmixtures, soaps, wax mixtures, oil mixtures, etc. As mentioned earlier, the hydrocarbon materials are highly effective dispersant media for the pigment and dye materials normally employed in cosmetic formulations. Hence, the C C isoparaffin hydrocarbon materials can be used in the place of typical ester dispersion media (Item (3) above) thereby permitting the formulation of make-up type materials without using the ester dispersion compositions.

DESCRIPTION OF THE PREFERRED EMBODIMENTS The utility of the isoparaffinic hydrocarbon materials as cosmetic ingredients is shown in the following formulations:

EXAMPLE I A pre-electric shave lotion was prepared by admixing Hexadccyl Alcohol (Branched chain) 30 EXAMPLE 2 A cationic hair conditioner was prepared from the following materials:

Weight Z Part A C -C isoparaffin fraction 15.0 Hexadecyl Alcohol (Branched chain) 5.0 5.0

Glycerol Monostearate -Continued Part A Weight it Stearyl Alcohol 5.0 Polyoxyethylene (20) Oleyl Ether 2.5 Dialkylaminoalkyl Palmitamide L0 Propyl-P Hydroxybenzoate 0 1 Part B Weight 7c Water, Deionized 60.6 Propylene Glycol, USP 5.0 Methyl-P-Hydroxybenzoate 0.2 Phosphoric Acid (85 wt. 9:) 0.2

Part C Weight lr Perfume oil 0.4

The conditioner was formulated by heating Part A to -75C. and Part B to 6570C. and then admixing the same with stirring. The resulting emulsion is then permitted to cool to 2550C. with stirring. Thereafter, Part C is added to the mixture to secure the final formulation.

EXAMPLE 3 A hair groom and conditioner was prepared from the following materials:

The product was prepared by first mixing Part B and Part C with stirring and then Part D with the initial B-C mixture. The B-C-D mixture is then heated 7075C. with stirring. Thereafter Part A is heated to 80C. with stirring and mixed with the B-C-D mixture. The A-B-C-D mixture is then cooled with stirring to 4045C. and then mixed with Part E. The final product is then permitted to cool to 2530C. with stirring and the mixture packaged.

EXAMPLE 4 An anhydrous rouge composition was prepared from the following constituents:

Part A Weight 7:

C|;CH isoparaffin fraction 35.5 Mineral oil (90 SSU viscosity at lOF.) 15.0 Microcrystalline wax 10.0 Camauba wax 6.0

Part 8 Weight Talc l0.0 Titanium Dioxide 20.0 Pigment 3.0 Propyl-p-hydroxybenzoate 0.15

Part C Weight Perfume Oil 0.5

The rouge is obtained by pre-blending Part B and then stirring the same with Part A which had been previously heated to 8085C. The mixing is desirably conducted in a roller mill. After the mixing operation, the A-B mixture is heated to 7075C. with stirring and then admixed with Part C.

EXAMPLE A waterless hand cleaner composition was prepared from the following materials:

Part A is heated to 80C. and then Part B heated to 90C. Parts A and B are then mixed with stirring and the mixture cooled to 80-85C. The A-B mixture is then admixed with Part C to obtain the final product.

EXAMPLE 6 A pre-electric shave lotion was prepared in the manner described in Example 1 except that in place of the C C isoparaffin fraction of the present invention, having a volatility in the range of about 225 to 255C. a C,,C, isoparafiin solvent having a volatility in the range of about 180 to 220 was employed.

EXAMPLE 7 The pre-electric shave lotions prepared in Example '1 and Example 6 were tested by human subjects who applied each to their face and then shaved.

The responses to the use of each lotion were as follows. The pre-shave lotion of Example 6 proved ineffective since it evaporated from the skin too rapidly to allow for proper lubrication and additionally caused an overall drying effect on the skin. The lotion prepared in accordance with Example 1 was highly effective in providing sufficient skin lubrication and a comfortable after-shave effect.

What is claimed is:

l. A cosmetic composition for lubricating the skin comprising an admixture of cosmetic conditioning materials in an oil and water emulsion including 0.5 to 50 weight percent, based on the total composition, of a lubricant C -C isoparaffinic hydrocarbon fraction boiling in the range of about 225 to 225C.

2. A process for lubricating the skin which comprises applying to the skin a cosmetic formulation comprising an admixture of cosmetic materials and a lubricating effective amount of from 0.5 to 50 weight percent based on total formulation of a C C isoparaffinic hydrocarbon fraction boiling in the range of about 225 to 255C.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2628205 *Oct 21, 1950Feb 10, 1953Res Prod CorpViscous hydrophilic composition and method of making the same
US3439088 *Jun 16, 1964Apr 15, 1969Exxon Research Engineering CoCosmetic preparations-wax rouge and foundation make-up
US3574827 *Dec 29, 1966Apr 13, 1971Exxon Research Engineering CoOintment base composition
Non-Patent Citations
Reference
1 *DeNavarre, The Chem. & Mfg. of Cos., 2nd ed, Vol. II, pp. 359 367.
2 *Wells et al., Cos. & The Skin, Reinhold Pub. N.Y., 1964, pp. 654 654.
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US4112167 *Jan 7, 1977Sep 5, 1978The Procter & Gamble CompanySkin cleansing product having low density wiping zone treated with a lipophilic cleansing emollient
US4117110 *Apr 14, 1977Sep 26, 1978Globol Werk GmbhGels, deodorizers
US4183898 *May 25, 1978Jan 15, 1980Liff Lawrence JLiquid base makeup composition
US4349535 *Jan 11, 1980Sep 14, 1982Liff Lawrence JWater, cellulose, chlorine dioxide; blood simulation
US4362747 *Aug 3, 1981Dec 7, 1982Eli Lilly And CompanyCosmetic cream pack formulation
US4374825 *Feb 17, 1981Feb 22, 1983The Proctor & Gamble CompanyHair conditioning compositions
US4387090 *Feb 13, 1981Jun 7, 1983The Procter & Gamble CompanyHair conditioning compositions
US4454118 *Dec 9, 1981Jun 12, 1984Johnson Zelma MMethod of treating psoriasis
US4472375 *Oct 1, 1982Sep 18, 1984The Procter & Gamble CompanyVolatile agent, nonionic polymeric thickener, quaternary ammonium salt, fatty amine salt
US4536405 *Sep 17, 1979Aug 20, 1985Shiseido Company Ltd.Make-up cosmetics composition
US4585650 *Oct 4, 1982Apr 29, 1986White Laboratories, Inc.Pre-shaving application
US4708813 *Oct 2, 1986Nov 24, 1987The Procter & Gamble CompanyNonlathering cleansing mousse with skin conditioning benefits
US4806262 *Nov 9, 1987Feb 21, 1989The Procter & Gamble CompanySurfactants and moisturizer; no rinsing
US4818751 *Dec 11, 1986Apr 4, 1989Zeria Shinyaku Kogyo Kabushiki KaishaCosmetics
US4873078 *Apr 22, 1988Oct 10, 1989Plough, Inc.Containing isohexadecane and a heterogeneous mixture of two distinctly different dyes
US4939179 *Jun 22, 1989Jul 3, 1990Chesebrough-Pond's Inc.Cosmetic emulsions with hydrocarbon thickening agents
US5021405 *Mar 5, 1990Jun 4, 1991Dow Corning CorporationEmollient durability enhancing siloxanes
US5072512 *May 18, 1990Dec 17, 1991Noujain Elie GReservoir razor for applying a thin film of metal lubricant onto the blade of the razor and method of shaving
US5280019 *Apr 11, 1991Jan 18, 1994Dow Corning CorporationPolydimethylsiloxne exhibiting humectant-like behavior
US5324507 *Feb 6, 1992Jun 28, 1994L'orealComposition for washing based on hydrocarbon oil and fatty alcohols containing ether and/or thioether or sulphoxide groups
US5372806 *Jul 9, 1992Dec 13, 1994Soft And ShineGrooming composition
US5444096 *Nov 9, 1993Aug 22, 1995Helene Curtis, Inc.Stable anhydrous topically-active composition and suspending agent therefor
US5453176 *Oct 13, 1993Sep 26, 1995Narloch; Bruce A.Process for preparing white oil containing a high proportion of isoparaffins
US5578310 *Jun 3, 1994Nov 26, 1996Berlex Laboratories Inc.Topical bioadhesive ointment compositions and their use in wound healing
US5654341 *Apr 11, 1995Aug 5, 1997The Andrew Jergens CompanyMixture of cationic surfactant, fatty acid and oil
US5911917 *Aug 21, 1997Jun 15, 1999Masters; Thomas R.Preserved cellular structures
US5997732 *Oct 14, 1998Dec 7, 1999Chevron U.S.A. Inc.Clay treatment process for white mineral oil
US6541017Jun 24, 1999Apr 1, 2003L'oreal S.A.Stable anhydrous formulation for cosmetic or pharmaceutical use, containing atlest one silicon oil, a pigment and an oxyalkylenated silicon substituted at alpha and omega positions
US6589538Jun 24, 1999Jul 8, 2003L'oreal S.A.Anhydrous composition and cosmetic, pharmaceutical or hygienic use
US7214382Jun 5, 2003May 8, 2007Adi SheferSelf-warming or self-heating cosmetic and dermatological compositions and method of use
US7264821Feb 14, 2003Sep 4, 2007L'orealStability, little transfer and very good dispersion of the pigments
US7271209Feb 19, 2004Sep 18, 2007Exxonmobil Chemical Patents Inc.Using simple nonfunctionalized hydrocarbon; low and high temperature applications; impact strength, toughness, flexibility; food containers, diapers, clothing, toys
US7531594Feb 19, 2004May 12, 2009Exxonmobil Chemical Patents Inc.Polyolefin, particularly a propylene polymer, and one or more non-functionalized plasticizers having a kinematic viscosity ("KV") of 2 cSt or less at 100 degrees C., such as paraffins, isoparaffins or olefin oligomers
US7619026Aug 12, 2003Nov 17, 2009Exxonmobil Chemical Patents Inc.Mixture with hydrocarbon
US7619027Oct 24, 2006Nov 17, 2009Exxonmobil Chemical Patents Inc.Improved pour points, processability, flexibility, softness, and impact resistance; films
US7622523Feb 9, 2005Nov 24, 2009Exxonmobil Chemical Patents Inc.sterilized article comprising a plasticized polyolefin composition comprising one or more polyolefins and one of more non-functionalized plasticizers
US7632887Aug 4, 2003Dec 15, 2009Exxonmobil Chemical Patents Inc.Plasticized polyolefin compositions
US7652092Apr 19, 2006Jan 26, 2010Exxonmobil Chemical Patents Inc.nucleation agents; flexibility
US7652093Apr 19, 2006Jan 26, 2010Exxonmobil Chemical Patents Inc.Improved pour points, processability, flexibility, softness, and impact resistance; films
US7652094May 12, 2006Jan 26, 2010Exxonmobil Chemical Patents Inc.Plasticized polyolefin compositions
US7858701Apr 3, 2008Dec 28, 2010Exxonmobil Chemical Patents Inc.Soft homogeneous isotactic polypropylene compositions
US7875670Feb 25, 2009Jan 25, 2011Exxonmobil Chemical Patents Inc.Articles from plasticized polyolefin compositions
US7906588Oct 6, 2008Mar 15, 2011Exxonmobil Chemical Patents Inc.Soft heterogeneous isotactic polypropylene compositions
US7985801Sep 13, 2007Jul 26, 2011Exxonmobil Chemical Patents Inc.polypropylene or polybutene and paraffinic hydrocarbon plasticizer having a number average molecular weight of 500 to 20,000; improve impact strength and toughness at low and high temperatures; nonbrittle; food containers, diapers, clothing, surgical gown
US7998579Apr 29, 2005Aug 16, 2011Exxonmobil Chemical Patents Inc.Polypropylene based fibers and nonwovens
US8003725Aug 15, 2006Aug 23, 2011Exxonmobil Chemical Patents Inc.Plasticized hetero-phase polyolefin blends
US8080583May 27, 2008Dec 20, 2011Elc Management LlcEmulsion cosmetic compositions containing resveratrol derivatives and linear or branched silicone
US8084496May 6, 2010Dec 27, 2011Elc Management LlcResveratrol ferulate compounds and compositions
US8084506Mar 20, 2009Dec 27, 2011Mary Kay Inc.Sebum absorption compositions
US8192813Jun 18, 2008Jun 5, 2012Exxonmobil Chemical Patents, Inc.Crosslinked polyethylene articles and processes to produce same
US8193155Feb 9, 2009Jun 5, 2012Elc Management, LlcMethod and compositions for treating skin
US8211968Jan 25, 2010Jul 3, 2012Exxonmobil Chemical Patents Inc.Plasticized polyolefin compositions
US8217112Oct 19, 2009Jul 10, 2012Exxonmobil Chemical Patents Inc.Plasticized polyolefin compositions
US8221731May 18, 2009Jul 17, 2012Aveda CorporationContinuous moisturization compositions
US8221732Jun 6, 2011Jul 17, 2012Aveda CorporationContinuous moisturization compositions
US8344024May 27, 2008Jan 1, 2013Elc Management LlcAnhydrous cosmetic compositions containing resveratrol derivatives
US8362076Nov 11, 2011Jan 29, 2013Elc Management LlcAscorbic acid esters of resveratrol and cosmetic compositions
US8389615Jul 7, 2006Mar 5, 2013Exxonmobil Chemical Patents Inc.Elastomeric compositions comprising vinylaromatic block copolymer, polypropylene, plastomer, and low molecular weight polyolefin
US8394394May 26, 2005Mar 12, 2013L'oréalMousse formulations
US8461200Nov 11, 2011Jun 11, 2013Elc Management LlcSalicylic acid esters of resveratrol and cosmetic compositions
US8465731Mar 12, 2010Jun 18, 2013Elc Management, LlcProbiotic color cosmetic compositions and methods
US8491921Feb 6, 2012Jul 23, 2013Elc Management, LlcCompositions and methods for tinting keratin material
US8513347Jul 7, 2006Aug 20, 2013Exxonmobil Chemical Patents Inc.Elastomeric compositions
US8529923Aug 4, 2009Sep 10, 2013Chanel Parfums BeauteCosmetic composition based on substantially hemispherical particles
US8535738Jul 7, 2008Sep 17, 2013Elc Management, LlcMethods and compositions for treating skin
US8703030Dec 31, 2010Apr 22, 2014Exxonmobil Chemical Patents Inc.Crosslinked polyethylene process
US8703161Jun 23, 2009Apr 22, 2014Elc Management, LlcSkin repair compositions comprising circadian gene activators and a synergistic combination of Sirt1 gene activators
US8722026Jan 4, 2011May 13, 2014Elc Management, LlcSkin lightening compositions
US8765156Apr 30, 2010Jul 1, 2014Elc Management LlcTopical compositions comprising inorganic particulates and an alkoxylated diphenylacrylate compound
US8822404 *Jun 10, 2011Sep 2, 2014Firmenich SaPerfuming compositions and uses thereof
US8840929Dec 3, 2013Sep 23, 2014Elc Management LlcCosmetic compositions with near infra-red (NIR) light-emitting material and methods therefor
US20080161418 *Feb 23, 2006Jul 3, 2008Markus DierkerOils prepared by Kolbe electrolysis of fatty acids
US20130079270 *Jun 10, 2011Mar 28, 2013Firmenich SaPerfuming compositions and uses thereof
USRE33429 *Feb 3, 1989Nov 6, 1990Dow Corning CorporationCrosslinked polymer beAD
EP0035899A2Mar 9, 1981Sep 16, 1981THE PROCTER & GAMBLE COMPANYHair conditioning composition and method of conditioning hair therewith
EP0113930A2 *Nov 23, 1983Jul 25, 1984Mitchell Lloyd SchlossmanImproved compressing aid for compressing powders
EP0400546A1 *May 28, 1990Dec 5, 1990Helene Curtis, Inc.Stable anhydrous compositions for topical delivery of active materials
EP0404331A2 *May 15, 1990Dec 27, 1990Unilever PlcCosmetic composition
EP0800820A2 *Mar 25, 1997Oct 15, 1997L'orealCosmetic composition comprising a pasty fatty material and volatile compounds
EP0859581A1Sep 16, 1996Aug 26, 1998L'orealComposition for treating keratinous material, including at least one silicone-grafted polymer with a polysiloxane backbone grafted by non-silicone organic monomers and at least one c 11-26? liquid hydrocarbon
EP2083043A1Aug 4, 2003Jul 29, 2009ExxonMobil Chemical Patents Inc.Plasticized polyolefin compositions
EP2338466A1 *Dec 17, 2010Jun 29, 2011L'OréalCosmetic composition containing at least one volatile linear alkane, at least one amine silicone having a particular content, and at least one vegetable oil
EP2338468A1 *Dec 16, 2010Jun 29, 2011L'OréalCosmetic composition comprising at least one volatile linear alkane, at least one cationic surfactant whereby the two components are in a specific ratio
EP2338469A1 *Dec 16, 2010Jun 29, 2011L'OréalUse of a cosmetic composition containing a linear volatile alcane and an associative non-ionic polymer for conditioning the hair
EP2535360A1Dec 18, 2007Dec 19, 2012ExxonMobil Research and Engineering CompanyProcess for fluid phase in-line blending of polymers
WO1993021905A1 *Apr 23, 1993Nov 11, 1993Berlex Biosciences Division OfBioadhesive solid mineral oil emulsion
WO2001017496A1 *Sep 8, 2000Mar 15, 2001Anna Louisa GomesSkin-balance moisturizing cream
WO2010027491A1Sep 4, 2009Mar 11, 2010Exxonmobil Research And Engineering CompanyProcess for feeding ethylene to polymerization reactors
WO2012174091A2Jun 13, 2012Dec 20, 2012The Procter & Gamble CompanyPERSONAL CARE COMPOSITIONS COMPRISING A pH TUNEABLE GELLANT AND METHODS OF USING
WO2012174096A2Jun 13, 2012Dec 20, 2012The Procter & Gamble CompanyPersonal care compositions comprising a di-amido gellant and methods of using
WO2012177757A2Jun 20, 2012Dec 27, 2012The Procter & Gamble CompanyPersonal care compositions comprising shaped abrasive particles
Classifications
U.S. Classification514/789, 514/939, 424/63, 514/940, 424/70.6, 424/64, 424/70.1, 514/846, 514/943, 514/845, 424/73, 424/70.7, 514/941, 514/942
International ClassificationA61K47/06, A61Q9/02, A61Q19/10, A61Q5/12, A61Q5/06, A61Q1/08, A61K8/31
Cooperative ClassificationY10S514/94, Y10S514/939, A61Q5/12, Y10S514/941, A61K8/31, Y10S514/846, A61Q9/02, A61K9/0014, Y10S514/943, Y10S514/845, A61Q1/08, Y10S514/942, A61Q5/06, A61Q19/10, A61K47/06
European ClassificationA61Q5/12, A61Q19/10, A61Q1/08, A61K47/06, A61Q9/02, A61K9/00M3, A61K8/31, A61Q5/06