WO2014029711A2 - Mild foaming make-up remover composition - Google Patents

Mild foaming make-up remover composition Download PDF

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Publication number
WO2014029711A2
WO2014029711A2 PCT/EP2013/067191 EP2013067191W WO2014029711A2 WO 2014029711 A2 WO2014029711 A2 WO 2014029711A2 EP 2013067191 W EP2013067191 W EP 2013067191W WO 2014029711 A2 WO2014029711 A2 WO 2014029711A2
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WO
WIPO (PCT)
Prior art keywords
foam
skin
composition
composition according
acyl
Prior art date
Application number
PCT/EP2013/067191
Other languages
French (fr)
Other versions
WO2014029711A3 (en
Inventor
Shota Morimoto
KURITA (nee USUI), Tomoko
Yukihiro Murata
Original Assignee
Unilever Plc
Unilever N.V.
Conopco, Inc., D/B/A Unilever
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Unilever Plc, Unilever N.V., Conopco, Inc., D/B/A Unilever filed Critical Unilever Plc
Priority to MX2015002280A priority Critical patent/MX352365B/en
Priority to EA201590177A priority patent/EA027395B1/en
Priority to CN201380044248.1A priority patent/CN104661636B/en
Priority to BR112015003693A priority patent/BR112015003693A2/en
Priority to JP2015527873A priority patent/JP6333253B2/en
Publication of WO2014029711A2 publication Critical patent/WO2014029711A2/en
Publication of WO2014029711A3 publication Critical patent/WO2014029711A3/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/046Aerosols; Foams
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/345Alcohols containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/361Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/14Preparations for removing make-up

Definitions

  • the invention concerns a make-up removing cosmetic composition that is
  • WO2008052956 published on May 8, 2008 to Kobayashi et al. describes a cleansing composition including a blend of non-saccharide polyhydric alcohol fatty acid triester(s) and saccharide alcohol fatty acid tetraester(s)in a specific ratio and blended with oil that removes makeup under moist conditions such as with wet hands without the problem of phase separation and compromised makeup removal efficiency.
  • the inventive product is used with a countertop mechanical pump allowing foam to be dispensed directly onto the hands.
  • the pump is situated in a stable position so that the hand or forearm can be used to depress the pump and dispense the product. This results in a more hygienic cleansing process.
  • initial dilution with water is not required since the foam can be readily distributed on the skin prior to rinsing.
  • the inventive product is preferably transparent. Transparency is herein defined as having a turbidity less than or equal to 105 NTU (Nephelometric Turbidity Units).
  • an aqueous, preferably transparent, preferably foaming, liquid composition for cleansing the skin including but not limited to: a. C8 to C18 soap(s) in a total concentration range of about 0.1 to 10 % by wt.; b. C10 to C14 acyl glycinate(s) in a total concentration range of about 5 to 25 % by wt.;
  • a packaged product for cleansing the skin comprising the above composition contained in a mechanical pump foam dispenser wherein a foam is dispensed.
  • a method of cleansing and removing waxy makeup from the skin of a user including but not limited to the steps of: a. dispensing as a foam, an effective amount of the above composition for
  • an aqueous, preferably transparent, preferably foaming, liquid composition for cleansing the skin including but not limited to: a. C8 to C18 soap(s) in a total concentration range of about 0.1 to 10 % by wt.; preferably 0.1 to 5.0 and more preferably 0.1 to 1 .0;
  • d. greater than about 30 % by wt. of water; preferably greater than 40.0 and more preferably greater than 50.0;
  • acyl arginine(s) to acyl glycinate(s) is less than about 0.008 preferably less than 0.007 and more preferably less than 0.005; and f. polyol(s) in a concentration of about 20 to 40.0 % by wt. preferably about 20.0 to 35.0 and more preferably about 25.0 to 35.0.
  • the ratio of acyl arginine(s) to acyl glycinate(s) is more than 0.0004 and preferably more than 0.002.
  • the minimum ratio of acyl arginine(s) to acyl glycinate(s) is in the range of 0.002 to 0.0004 and preferably in the range of 0.002 to 0.005.
  • the composition is preferably an aqueous transparent foaming liquid composition for cleansing the skin.
  • the inventive composition further includes C8 to C12 glucoside(s) in a total concentration of about 1 to 5 % by wt. preferably about 1.0 to 4.0 and more preferably about 1 .0 to 3.0.
  • C8 to C12 hydroxysultaine(s) in a total concentration of about 1 to 5 % by wt. preferably about 1.0 to 4.0 and more preferably about 1 .0 to 3.0.
  • the viscosity at 25 C of the inventive composition is less than 40.0 mPas, preferably less than 35.0 mPas and more preferably less than 30.0 mPas.
  • a packaged product for cleansing the skin comprising the above composition contained in a mechanical pump foam dispenser wherein a foam is dispensed.
  • C8 - C18 alkyl carboxylic acid soaps are used for the invention.
  • carboxylic acid soap(s) such as lauric (C12), myristic (C14), palmitic (C16) or stearic (C18) soaps are used alone or in combination.
  • the soap(s) are used at levels as low as 0.1 % by wt. and at levels as high as 1 , 5 or 10 % by wt.
  • One or more C10-C14 acyl glycinate(s) are used in the inventive composition.
  • the inventive composition also contains one or more acyl arginates having the following formula wherein R can have values from 10 through 14 and preferably represents an unbranched alkyi chain of 1 1 (lauroyl arginate)
  • anionic detergent actives which may be used in the invention may be aliphatic sulfonates, such as a primary alkane (e.g., C 8 -C 2 2) sulfonate, primary alkane (e.g., C 8 - C 22 ) disulfonate, C 8 -C 2 2 alkene sulfonate, C 8 -C 2 2 hydroxyalkane sulfonate or alkyi glyceryl ether sulfonate (AGS); or aromatic sulfonates such as alkyi benzene sulfonate.
  • a primary alkane e.g., C 8 -C 2 2 2 2
  • primary alkane e.g., C 8 - C 22
  • disulfonate C 8 -C 2 2 alkene sulfonate
  • C 8 -C 2 2 2 alkene sulfonate C 8 -C 2 2 hydroxyalkane s
  • the anionic may also be an alkyi sulfate (e.g., Ci 2 -Ci 8 alkyi sulfate) or alkyi ether sulfate (including alkyi glyceryl ether sulfates).
  • alkyi ether sulfates are those having the formula:
  • RO(CH 2 CH 2 0) n S0 3 M wherein R is an alkyl or alkenyl having 8 to 18 carbons, preferably 12 to 18 carbons, n has an average value of greater than 1 .0, preferably greater than 3; and M is a solubilizing cation such as sodium, potassium, ammonium or substituted ammonium. Ammonium and sodium lauryl ether sulfates are preferred.
  • the anionic may also be alkyl sulfosuccinates (including mono- and dialkyl, e.g., C 6 -C 2 2 sulfosuccinates); alkyl and acyl taurates, alkyl and acyl sarcosinates, sulfoacetates, C 8 - C 22 alkyl phosphates and phosphates, alkyl phosphate esters and alkoxyl alkyl phosphate esters, acyl lactates, C 8 -C 2 2 monoalkyl succinates and maleates, sulphoacetates, alkyl glucosides and acyl isethionates, and the like.
  • alkyl sulfosuccinates including mono- and dialkyl, e.g., C 6 -C 2 2 sulfosuccinates
  • alkyl and acyl taurates alkyl and acyl sarcosinates,
  • Sulfosuccinates may be monoalkyl sulfosuccinates having the formula: R 4 0 2 CCH 2 CH(S0 3 M)C0 2 M; and amide-MEA sulfosuccinates of the formula;
  • R 4 CONHCH 2 CH 2 0 2 CCH 2 CH(S0 3 M)C0 2 M, wherein R 4 ranges from C 8 -C 22 alkyl and M is a solubilizing cation.
  • Sarcosinates are generally indicated by the formula: R 1 CON(CH 3 )CH 2 C0 2 M, wherein R 1 ranges from C 8 -C 20 alkyl and M is a solubilizing cation.
  • Taurates are generally identified by formula: R 2 CONR 3 CH 2 CH 2 S0 3 M, wherein R 2 ranges from C 8 -C 2 o alkyl, R 3 ranges from C1-C4 alkyl and M is a solubilizing cation.
  • One or more polyols are present in compositions of this invention. These polyols may be monomeric or polymeric. Monomeric polyols may have from 1 to 20 carbon atoms and from 2 to 10 hydroxyls. Illustrative monomeric polyols include glycerin, propylene glycol; 1 ,4-butane diol; 1 ,3-butane diol; 1 ,2-butane diol; 1 -6-hexanediol, 1 ,2-hexane diol; 3-methyl-1 ,3-butane diol; 2-methyl-1 , 3-propane diol, sorbitol and mixtures thereof and the like. Particularly preferred are glycerin, propylene glycol, and 1 ,3-butane diol.
  • Polymeric polyols are illustrated by polypropylene glycol, polyethylene glycol, dipropylene glycol, diglycerol, polyglycerol, trimethylene glycol, dipentaerythritol and combinations thereof and the like.
  • nonionic and amphoteric surfactants may be employed as optional further components of the present invention.
  • the nonionic surfactants ordinarily are based upon a hydrophobe unit such as a fatty alcohol or a fatty acid having from about 10 to about 22 carbon atoms, an alkyl phenol having from about 6 to about 12 carbon atoms in the alkyl chain, sorbitan and mixtures thereof.
  • hydrophobes ordinarily will be condensed with a hydrophilic unit, particularly from 1 to about 50, preferably from about 10 to about 30 moles of ethylene oxide, propylene oxide, butylene oxide or mixtures thereof.
  • Illustrative materials are POE-20 sorbitan monolaurate; POE-20 cetyl ether; POE-7 glyceryl cocoate; POE-15 stearyl ether; POE-10 stearyl ether; POE-15 palmityl ether and combinations thereof and the like.
  • Other useful nonionics are alkyl polyglycosides such as lauryl polyglucoside available from the BASF Corporation and Kao Corp.
  • Another class of nonionic emulsifiers are the long chain tertiary amine oxides. Examples include dimethyldodecylamine oxide, dimethylhexadecylamine oxide; di(2-hydroxy)tetradecylamine oxide, dimethyldecylamine oxide and combinations thereof and the like.
  • Amphoteric surfactants such as betaines and sultaines may also be employed.
  • Suitable examples include C8 - C12 hydroxy sultaines, e.g. lauryl hydroxy sultaine, cocamidopropyl betaine, cocoamido sultaine, dodecyl dimethyl betaine, cetyl dimethyl betaine and combinations thereof and the like.
  • Amounts of the nonionic surfactants may range each from about 0.1 to about 10%, preferably from about 0.2 to about 5%, optimally from about 0.3 to about 7% by weight of the composition.
  • Amounts of the amphoteric surfactants may range each from about 0.1 to about 10%, preferably from about 0.2 to about 5%, optimally from about 0.3 to about 7% by weight of the composition.
  • Water is preferably present in an amount of greater than about 30 % by wt., preferably greater than 40.0 wt% and more preferably greater than 50.0 wt%.
  • the amount of water is preferably less than 75 wt%.
  • Water is preferably present in an amount of from 30 wt% to 75 wt%.
  • Preservatives will usually also be incorporated into the inventive formulations.
  • Representative materials include phenoxyethanol, methylparaben, propyl paraben, ethylenediamine tetra acetate (EDTA) salts, benzyl alcohol, lodopropynyl butyl carbamate, DMDM Hydantoin, caprylyl glycol and combinations thereof and the like. Amounts of these materials may range anywhere from about 0.0001 to about 1 % by weight of the composition.
  • Optional minor components may include colorants, fragrances, promotional agents, and/or promotional agents.
  • compositions of the present invention preferably are free of any oil phase, especially free of water insoluble emollients.
  • free means less than 0.05%, preferably less than 0.01 % emollient, and water insoluble means any emollient having a solubility in distilled water at 25 C of less than about 1 gm per 100 mL, more preferably less than about 0.1 gm per 100 mL. Absent water insoluble emollients, the compositions can be transparent and have improved foamability.
  • the viscosity of the inventive composition is preferably in the range of 1 to 50 mPas, preferably 1 to 40 mPas at 25 C as measured by a Brookfield Model LVDV-II+, Spindle No LV1 , using 60 rpm and 1 min measurement time.
  • a preferred embodiment of the cleansing product according to this invention is a non- aerosol foaming dispenser containing the inventive composition.
  • the inventive composition is dispensed as a foam and produces long-lasting and copious foam in contact with wet skin.
  • a suitable dispenser is mechanical and is generally characterized by a container for storing the composition (preferably a transparent container), a dispensing head defined by a housing containing a pump, and a dip tube for transferring the composition from the container into the dispensing head.
  • Foam is created by requiring the composition to pass through a screen material which may be a porous substance such as a sintered material, a wire (plastic or metal) gauze screen or similar structures. Preferably two screens are used.
  • Suitable mechanical dispensers are described in U.S. Pat. No. 3,709,437 (Wright), U.S. Pat. No. 3,937,364 (Wright), U.S. Pat. No. 4,022,351 (Wright), U.S. Pat. No.
  • a preferred foamer is the F5L pump foamer head manufactured by Daiwa Corporation located in (Tokyo, Japan). This foamer was used to conduct the foam stability studies and the ease of pumping studies discussed in Example 1 .
  • the F5L device has the following characteristics: Mesh Size: 255 Mesh (Upper) / 200 (Lower)
  • Air/Liquid ratio 9.5 / 1
  • foaming dispensers may include squeeze foamers.
  • Squeeze foamer packages are well known as exemplified by the disclosures in the following patents that are incorporated herein by reference.
  • the composition When squeeze foamers are used, the composition is placed in the container reservoir (plastic squeeze bottle). Squeezing the container with the hand forces the composition through a foamer head, or other foam producing means, where the composition is mixed with air and then through a homogenizing means that makes the foam more homogeneous and controls the consistency of the foam. The foam is then discharged as a uniform, non-pressurized aerated foam.
  • Instruments to be used with this protocol may include but are not limited to the ServoMed Evaporimeter with EP1 or EP2 probe (SeroMed AB, Sweden), Corneometer CM820 (COURAGE+KHAZAKA electronic GmbH, Cologne, Germany), the Skicon Skin Hygrometer with the MT-8C probe (I.B.S CO., LTD., Shizuoka-ken, Japan), and the Moisture Checker (STR - School & Science Technology Resources, Scotts Valley, Ca). The room temperature will be maintained at 68° to 77° F and 30% to 40% Relative Humidity. Moisturization will be defined as mean change from baseline of (visual dryness or skin hydration).
  • the acceptability of formulation transparency or clarity can be measured qualitatively and quantitively using a visual method of turbidity determination and a turbidimeter respectively.
  • the visual method involves looking through a determined path length of the formulation to a visual target and determining if the visual target is legible or recognizable.
  • This target may be a straight line, a set of parallel lines, a number or a letter printed on white paper.
  • Turbidity may be quantitatively determined by a Turbidimeter, Model DRT-100D, manufactured by Shaban Manufacturing Inc, H. F. Instruments Division using a sample cuvette of 28 mm diameter by 91 mm in length with a flat bottom. Samples that receive a 'pass' rating from the visual method are expected to have a turbidity measurement of less than or equal to 105 NTU's (Nephelometric Turbidity Units).

Abstract

A make-up remover composition suitable for dispensing from a mechanical pump foamer is provided for abundant and long-lasting foam properties on wet skin as well as on dry waxy makeup. The foam remains stable at –5 C. The inventive make-up remover composition also is expected to provide an enhanced moisturizing feeling to the skin after rinsing compared to comparative products. The composition includes a specific minimum ratio of C10-C14 acyl argininate to C10-C14 acyl glycinate in an aqueous polyol surfactant matrix.

Description

MILD FOAMING MAKE-UP REMOVER COMPOSITION
BACKGROUND OF THE INVENTION 1 . Field of the Invention
The invention concerns a make-up removing cosmetic composition that is
advantageously dispensed by a non-aerosol pump foamer dispenser as a long-lasting foam.
2. Background of the Art
An important segment of the cosmetics market are products which are utilized for removing make-up. Removal of pigments of eye shadow, mascara, blush, lipstick and face powder is a daily problem for many women. The problem has been addressed through formulations which may include materials operating by solvent action or by emulsification, for example, O/W emulsion cream, Gel, Oil, or Sheet type product formats are available. Recently, makeup remover compositions by a pump foamer dispenser have been introduced to the market to enable persons to conveniently use in the shower or bath i.e. with wet hands, and to dispense the product as foam for rapid action on the skin without dripping.
WO2008052956 published on May 8, 2008 to Kobayashi et al. describes a cleansing composition including a blend of non-saccharide polyhydric alcohol fatty acid triester(s) and saccharide alcohol fatty acid tetraester(s)in a specific ratio and blended with oil that removes makeup under moist conditions such as with wet hands without the problem of phase separation and compromised makeup removal efficiency.
Surprisingly a formulation including a blend of an acyl glycinate(s) and acyl argininate(s) in a specific ratio range, blended with polyol(s) and water was found to produce considerable and long-lasting foam when dispensed on wet skin and to also cleanse and with the expectation to moisturize the skin compared to comparative makeup remover products. Furthermore the inventive product did not have the problem of phase separation and insufficient foaming volume at low temperature of -5 C seen for comparative and prior art products.
Preferably the inventive product is used with a countertop mechanical pump allowing foam to be dispensed directly onto the hands. Preferably the pump is situated in a stable position so that the hand or forearm can be used to depress the pump and dispense the product. This results in a more hygienic cleansing process. In addition, initial dilution with water is not required since the foam can be readily distributed on the skin prior to rinsing. The inventive product is preferably transparent. Transparency is herein defined as having a turbidity less than or equal to 105 NTU (Nephelometric Turbidity Units).
BRIEF DESCRIPTION OF THE INVENTION In one aspect of the invention is an aqueous, preferably transparent, preferably foaming, liquid composition for cleansing the skin including but not limited to: a. C8 to C18 soap(s) in a total concentration range of about 0.1 to 10 % by wt.; b. C10 to C14 acyl glycinate(s) in a total concentration range of about 5 to 25 % by wt.;
c. C10 to C14 acyl arginine(s) in a total concentration range of about 0.01 to 0.1 % by wt.;
d. greater than about 30 % by wt. of water;
e. wherein the ratio of acyl arginine(s) to acyl glycinate(s) is less than about 0.008; and
f. polyol(s) in a concentration of about 20 to 40.0 % by wt.
In another preferred embodiment is a packaged product for cleansing the skin comprising the above composition contained in a mechanical pump foam dispenser wherein a foam is dispensed. In a further preferred embodiment is a method of cleansing and removing waxy makeup from the skin of a user including but not limited to the steps of: a. dispensing as a foam, an effective amount of the above composition for
removing oily makeup from wet skin;
b. applying the foam to the wet skin;
c. rubbing the foam on the wet skin for a time sufficient to disperse the oily
makeup residing on the skin; and
d. rinsing the foamed composition and dispersed oily makeup from the skin.
DETAILED DESCRIPTION OF THE INVENTION
All publications and patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety.
In one aspect of the invention is an aqueous, preferably transparent, preferably foaming, liquid composition for cleansing the skin including but not limited to: a. C8 to C18 soap(s) in a total concentration range of about 0.1 to 10 % by wt.; preferably 0.1 to 5.0 and more preferably 0.1 to 1 .0;
b. C10 to C14 acyl glycinate(s) in a total concentration range of about 5 to 25 % by wt.; preferably 5.0 to 15.0 and more preferably 10.0 to 15.0;
c. C10 to C14 acyl arginine(s) in a total concentration range of about 0.01 to 0.1 % by wt.; preferably 0.01 to 0.08 and more preferably 0.02 to 0.08;
d. greater than about 30 % by wt. of water; preferably greater than 40.0 and more preferably greater than 50.0;
e. wherein the ratio of acyl arginine(s) to acyl glycinate(s) is less than about 0.008 preferably less than 0.007 and more preferably less than 0.005; and f. polyol(s) in a concentration of about 20 to 40.0 % by wt. preferably about 20.0 to 35.0 and more preferably about 25.0 to 35.0.
In a preferred embodiment, the ratio of acyl arginine(s) to acyl glycinate(s) is more than 0.0004 and preferably more than 0.002. Advantageously the minimum ratio of acyl arginine(s) to acyl glycinate(s) is in the range of 0.002 to 0.0004 and preferably in the range of 0.002 to 0.005.
The composition is preferably an aqueous transparent foaming liquid composition for cleansing the skin.
Advantageously the inventive composition further includes C8 to C12 glucoside(s) in a total concentration of about 1 to 5 % by wt. preferably about 1.0 to 4.0 and more preferably about 1 .0 to 3.0. Preferably also included is C8 to C12 hydroxysultaine(s) in a total concentration of about 1 to 5 % by wt. preferably about 1.0 to 4.0 and more preferably about 1 .0 to 3.0. More preferably the viscosity at 25 C of the inventive composition is less than 40.0 mPas, preferably less than 35.0 mPas and more preferably less than 30.0 mPas. In another preferred embodiment is a packaged product for cleansing the skin comprising the above composition contained in a mechanical pump foam dispenser wherein a foam is dispensed.
In a further preferred embodiment is a method of cleansing and removing waxy makeup from the skin of a user including but not limited to the steps of: a. dispensing as a foam an effective amount of the above composition for
removing oily makeup from wet skin;
b. applying the foam to the wet skin;
c. rubbing the foam on the wet skin for a time sufficient to disperse the oily
makeup residing on the skin; and
d. rinsing the foamed composition and dispersed oily makeup from the skin.
Soaps
Normal C8 - C18 alkyl carboxylic acid soaps are used for the invention. Preferably carboxylic acid soap(s), such as lauric (C12), myristic (C14), palmitic (C16) or stearic (C18) soaps are used alone or in combination. Advantageously the soap(s) are used at levels as low as 0.1 % by wt. and at levels as high as 1 , 5 or 10 % by wt.
Synthetic anionic surfactants
One or more C10-C14 acyl glycinate(s) are used in the inventive composition.
Preferably it is used at levels as low as 5 or 10 % by wt. and at levels as high as 15, 20 or 25 % by wt. The inventive composition also contains one or more acyl arginates having the following formula wherein R can have values from 10 through 14 and preferably represents an unbranched alkyi chain of 1 1 (lauroyl arginate)
Figure imgf000006_0001
Other anionic detergent actives which may be used in the invention may be aliphatic sulfonates, such as a primary alkane (e.g., C8-C22) sulfonate, primary alkane (e.g., C8- C22) disulfonate, C8-C22 alkene sulfonate, C8-C22 hydroxyalkane sulfonate or alkyi glyceryl ether sulfonate (AGS); or aromatic sulfonates such as alkyi benzene sulfonate. The anionic may also be an alkyi sulfate (e.g., Ci2-Ci8 alkyi sulfate) or alkyi ether sulfate (including alkyi glyceryl ether sulfates). Among the alkyi ether sulfates are those having the formula:
RO(CH2CH20)nS03M wherein R is an alkyl or alkenyl having 8 to 18 carbons, preferably 12 to 18 carbons, n has an average value of greater than 1 .0, preferably greater than 3; and M is a solubilizing cation such as sodium, potassium, ammonium or substituted ammonium. Ammonium and sodium lauryl ether sulfates are preferred.
The anionic may also be alkyl sulfosuccinates (including mono- and dialkyl, e.g., C6-C22 sulfosuccinates); alkyl and acyl taurates, alkyl and acyl sarcosinates, sulfoacetates, C8- C22 alkyl phosphates and phosphates, alkyl phosphate esters and alkoxyl alkyl phosphate esters, acyl lactates, C8-C22 monoalkyl succinates and maleates, sulphoacetates, alkyl glucosides and acyl isethionates, and the like.
Sulfosuccinates may be monoalkyl sulfosuccinates having the formula: R402CCH2CH(S03M)C02M; and amide-MEA sulfosuccinates of the formula;
R4CONHCH2CH202CCH2CH(S03M)C02M, wherein R4 ranges from C8-C22 alkyl and M is a solubilizing cation. Sarcosinates are generally indicated by the formula: R1CON(CH3)CH2C02M, wherein R1 ranges from C8-C20 alkyl and M is a solubilizing cation.
Taurates are generally identified by formula: R2CONR3CH2CH2S03M, wherein R2 ranges from C8-C2o alkyl, R3 ranges from C1-C4 alkyl and M is a solubilizing cation.
Polyols
One or more polyols are present in compositions of this invention. These polyols may be monomeric or polymeric. Monomeric polyols may have from 1 to 20 carbon atoms and from 2 to 10 hydroxyls. Illustrative monomeric polyols include glycerin, propylene glycol; 1 ,4-butane diol; 1 ,3-butane diol; 1 ,2-butane diol; 1 -6-hexanediol, 1 ,2-hexane diol; 3-methyl-1 ,3-butane diol; 2-methyl-1 , 3-propane diol, sorbitol and mixtures thereof and the like. Particularly preferred are glycerin, propylene glycol, and 1 ,3-butane diol.
Polymeric polyols are illustrated by polypropylene glycol, polyethylene glycol, dipropylene glycol, diglycerol, polyglycerol, trimethylene glycol, dipentaerythritol and combinations thereof and the like.
Nonionic and Amphoteric Surfactants
A variety of nonionic and amphoteric surfactants may be employed as optional further components of the present invention. The nonionic surfactants ordinarily are based upon a hydrophobe unit such as a fatty alcohol or a fatty acid having from about 10 to about 22 carbon atoms, an alkyl phenol having from about 6 to about 12 carbon atoms in the alkyl chain, sorbitan and mixtures thereof. These hydrophobes ordinarily will be condensed with a hydrophilic unit, particularly from 1 to about 50, preferably from about 10 to about 30 moles of ethylene oxide, propylene oxide, butylene oxide or mixtures thereof. Illustrative materials are POE-20 sorbitan monolaurate; POE-20 cetyl ether; POE-7 glyceryl cocoate; POE-15 stearyl ether; POE-10 stearyl ether; POE-15 palmityl ether and combinations thereof and the like. Other useful nonionics are alkyl polyglycosides such as lauryl polyglucoside available from the BASF Corporation and Kao Corp. Another class of nonionic emulsifiers are the long chain tertiary amine oxides. Examples include dimethyldodecylamine oxide, dimethylhexadecylamine oxide; di(2-hydroxy)tetradecylamine oxide, dimethyldecylamine oxide and combinations thereof and the like.
Amphoteric surfactants such as betaines and sultaines may also be employed.
Suitable examples include C8 - C12 hydroxy sultaines, e.g. lauryl hydroxy sultaine, cocamidopropyl betaine, cocoamido sultaine, dodecyl dimethyl betaine, cetyl dimethyl betaine and combinations thereof and the like.
Amounts of the nonionic surfactants may range each from about 0.1 to about 10%, preferably from about 0.2 to about 5%, optimally from about 0.3 to about 7% by weight of the composition. Amounts of the amphoteric surfactants may range each from about 0.1 to about 10%, preferably from about 0.2 to about 5%, optimally from about 0.3 to about 7% by weight of the composition.
Miscellaneous components
Water is preferably present in an amount of greater than about 30 % by wt., preferably greater than 40.0 wt% and more preferably greater than 50.0 wt%. The amount of water is preferably less than 75 wt%. Water is preferably present in an amount of from 30 wt% to 75 wt%.
Preservatives will usually also be incorporated into the inventive formulations.
Representative materials include phenoxyethanol, methylparaben, propyl paraben, ethylenediamine tetra acetate (EDTA) salts, benzyl alcohol, lodopropynyl butyl carbamate, DMDM Hydantoin, caprylyl glycol and combinations thereof and the like. Amounts of these materials may range anywhere from about 0.0001 to about 1 % by weight of the composition.
Optional minor components may include colorants, fragrances, promotional
ingredients, each in their effective amounts to accomplish their respective functions. Typical promotional ingredients include vitamins such as retynyl palmitate, tocopherol acetate and niacinamide. Other promotional ingredients include conjugated linoleic acid, ceramides, pentapeptides and combinations thereof. Compositions of the present invention preferably are free of any oil phase, especially free of water insoluble emollients. The term "free" means less than 0.05%, preferably less than 0.01 % emollient, and water insoluble means any emollient having a solubility in distilled water at 25 C of less than about 1 gm per 100 mL, more preferably less than about 0.1 gm per 100 mL. Absent water insoluble emollients, the compositions can be transparent and have improved foamability.
The viscosity of the inventive composition is preferably in the range of 1 to 50 mPas, preferably 1 to 40 mPas at 25 C as measured by a Brookfield Model LVDV-II+, Spindle No LV1 , using 60 rpm and 1 min measurement time.
Non-aerosol foaming dispenser
A preferred embodiment of the cleansing product according to this invention is a non- aerosol foaming dispenser containing the inventive composition. The inventive composition is dispensed as a foam and produces long-lasting and copious foam in contact with wet skin.
A suitable dispenser is mechanical and is generally characterized by a container for storing the composition (preferably a transparent container), a dispensing head defined by a housing containing a pump, and a dip tube for transferring the composition from the container into the dispensing head. Foam is created by requiring the composition to pass through a screen material which may be a porous substance such as a sintered material, a wire (plastic or metal) gauze screen or similar structures. Preferably two screens are used. Suitable mechanical dispensers are described in U.S. Pat. No. 3,709,437 (Wright), U.S. Pat. No. 3,937,364 (Wright), U.S. Pat. No. 4,022,351 (Wright), U.S. Pat. No. 4,147,306 (Bennett), U.S. Pat. No. 4,184,615 (Wright), U.S. Pat. No. 4,598,862 (Rice), U.S. Pat. No. 4,615,467 (Grogan et al.) and U.S Pat. No. 5,364,031 (Tamiguchi et al.). All these patents are incorporated herein by reference. A preferred foamer is the F5L pump foamer head manufactured by Daiwa Corporation located in (Tokyo, Japan). This foamer was used to conduct the foam stability studies and the ease of pumping studies discussed in Example 1 . The F5L device has the following characteristics: Mesh Size: 255 Mesh (Upper) / 200 (Lower)
Air/Liquid ratio: 9.5 / 1
Volume per 1 push: 0.95g
Other suitable foaming dispensers may include squeeze foamers. Squeeze foamer packages are well known as exemplified by the disclosures in the following patents that are incorporated herein by reference. U.S. Pat. Nos.: 3,709,437, Wright, issued Jan. 9, 1973; 3,937,364, Wright, issued Feb. 10, 1976; 4,022,351 , Wright, issued May 10, 1977; 4,147,306, Bennett, issued Apr. 3, 1979; 4,184,615, Wright, issued Jan. 22, 1980; 4,598,862, Rice, issued July 8, 1986; and 4,615,467, Grogan et al., issued Oct. 7, 1986; and French Pat. 2,604,622, Verhulst, published Apr. 8, 1988.
When squeeze foamers are used, the composition is placed in the container reservoir (plastic squeeze bottle). Squeezing the container with the hand forces the composition through a foamer head, or other foam producing means, where the composition is mixed with air and then through a homogenizing means that makes the foam more homogeneous and controls the consistency of the foam. The foam is then discharged as a uniform, non-pressurized aerated foam.
The invention will now be described in greater detail by way of the following non- limiting example. The example is for illustrative purposes only and not intended to limit the invention in any way. Physical test methods are described below:
Except in the operating and comparative examples, or where otherwise explicitly indicated, all numbers in this description indicating amounts or ratios of materials or conditions of reaction, physical properties of materials and/or use are to be understood as modified by the word "about".
Where used in the specification, the term "comprising" is intended to include the presence of stated features, integers, steps, components, but not to preclude the presence or addition of one or more features, integers, steps, components or groups thereof.
All percentages in the specification and examples are intended to be by weight unless stated otherwise.
Example 1
A series of inventive and comparative examples were made according to Tables 1 using the procedure described below in order to evaluate clarity, foam stability on contact with a wet substrate and on dry makeup foundation and ease of pumping foam with the F5L foamer pump at -5 C described above.
TABLE 1
Figure imgf000013_0001
* wt. % on active basis
(1 ) - (4) see procedures below
Based on the results reported in Table 1 , it is evident that greatest foam stability under both wet and dry conditions and ease of pumping was generally better for the inventive sample when compared to the comparative samples.
Test Methods: (1 ) Solubility:
Add Amisafe to Amilite GCK-12K at 20 C (RT) followed by heating up to 80C with stirring. If it is dissolved after 10 minutes at 80 C then the grading is ΌΚ". If there are visible insoluble materials remaining after 10 minutes then the grading is "NG".
(2) Foam Stability on a wet surface
1. Wet a paper towel uniformly with water without pooling the water.
2. Dispense about 0.7g of the sample from the F5L pump foamer on the wet towel.
3. Observe foam properties after 15min under ambient conditions in air at
approx. 20 C (RT) and 50% RH.
4. Grade the foam stability as follows: + TOTAL FOAM COLLAPSE
++ SOME FOAM COLLAPSE
+++ VERY LITTLE FOAM COLLAPSE
(3)Foam stability on dry make-up foundation 1. Apply 0.2g of foundation (Shiseido MAQUILLAGE Lasting Liquid UV, Ochre 10 All Season Type available from Shiseido, Tokyo, Japan) in a 1.5cm X15cm homogeneous square pattern on a polypropylene plastic board.
2. Let dry for 10min under ambient conditions in air at approx. 20 C (RT) and 50% RH.
3. Dispense about 0.7g of samples from the F5L pump foamer on the dried
foundation.
4. Observe foam stability after 15min under ambient conditions in air at approx.
20 C (RT) and 50% RH.
5. Grade the foam stability as follows: + TOTAL FOAM COLLAPSE
++ SOME FOAM COLLAPSE +++ VERY LITTLE FOAM COLLAPSE (4) Ease of dispensing foam from pump
Fill a container with the liquid cleansing product while leaving an air space. Seal with an F5L pump foamer head manufactured by Daiwa Corporation (Tokyo, Japan). Depress the pump and observe if foam is dispensed. If foam is dispensed, rate the ease of dispensing foam from the pump as ΌΚ". If no foam is dispensed (e.g. only a liquid is dispensed) rate the ease of dispensing foam from the pump as "NG". (5) Moisturization test:
1. Assemble a panel of trained persons.
2. Put about 3 g of one test sample on the right forearm of each panelist.
3. Rinse with tap water at ambient temperature for a few minutes. 4. Towel Dry, then grade moisturizing feeling using a maximum score of 5 points per panelist, then sum all the grades.
5. Repeat using about 3g of the comparative test sample on the left forearms of each panelist.
6. Alternatively a suitable instrumental method may be used to compare skin
moisturization between samples. All instrumental evaluations will be taken following a 30-minute acclimation period. The indoor humidity and temperature data will be recorded and included in the final report. Instrumental measurements may be taken at some or all of the following time points: 0, 1 , 2, 4, 6, 8 and 24 hours after product application.
Instruments to be used with this protocol may include but are not limited to the ServoMed Evaporimeter with EP1 or EP2 probe (SeroMed AB, Stockholm, Sweden), Corneometer CM820 (COURAGE+KHAZAKA electronic GmbH, Cologne, Germany), the Skicon Skin Hygrometer with the MT-8C probe (I.B.S CO., LTD., Shizuoka-ken, Japan), and the Moisture Checker (STR - School & Science Technology Resources, Scotts Valley, Ca). The room temperature will be maintained at 68° to 77° F and 30% to 40% Relative Humidity. Moisturization will be defined as mean change from baseline of (visual dryness or skin hydration).
(6) Procedure for preparing the examples illustrated in Table 1 :
1. Dissolve Amisafe in Amilite GCK-12K at 80C (Phase 1 ) until the solution is clear. 2. Mix Water and Glycerin at 80C until homogeneous (Phase 2)
3. Add Phase 1 to Phase 2 at 80C and blend.
4. Add NONSOUL LK-30 at 80C and blend.
5. Add Amphitol, Mydol12 and blend well. 6. Cool down to 35C
(7) Turbidity
For the purposes of this invention, the acceptability of formulation transparency or clarity can be measured qualitatively and quantitively using a visual method of turbidity determination and a turbidimeter respectively. Briefly, the visual method involves looking through a determined path length of the formulation to a visual target and determining if the visual target is legible or recognizable. This target may be a straight line, a set of parallel lines, a number or a letter printed on white paper. Place test formulation in a glass beaker such that the height from the bottom of the beaker to the top surface of the formulation is four inches. Make sure the formulation is free of air bubbles. Place the piece of paper with the visual target under the beaker. Look through the top surface of the formulation to the visual target. If the visual target appears similar to the original, the formulation is of acceptable clarity and receives a 'pass' rating. If the visual target appears significantly hazy, or is out of focus, compared to the original target, the formulation is of unacceptable clarity and receives a 'fail' rating. Turbidity may be quantitatively determined by a Turbidimeter, Model DRT-100D, manufactured by Shaban Manufacturing Inc, H. F. Instruments Division using a sample cuvette of 28 mm diameter by 91 mm in length with a flat bottom. Samples that receive a 'pass' rating from the visual method are expected to have a turbidity measurement of less than or equal to 105 NTU's (Nephelometric Turbidity Units). Samples that receive a 'fail' rating from the visual method will have a turbidity measurement of greater than 105 NTU's. The foregoing description and examples illustrate selected embodiments of the present invention. In light thereof variations and modifications will be suggested to one skilled in the art, all of which are within the scope and spirit of this invention.

Claims

J9233(C) CPL WO 2014/029711 PCT/EP2013/067191 18 Claims
1 . An aqueous, liquid composition for cleansing the skin comprising: a. C8 to C18 soap(s) in a total concentration range of about 0.1 to 10 % by wt; b. C10 to C14 acyl glycinate(s) in a total concentration range of about 5 to 25 % by wt.;
c. C10 to C14 acyl arginine(s) in a total concentration range of about 0.01 to 0.1 % by wt.;
d. greater than about 30 % by wt. of water;
e. wherein the ratio of acyl arginine(s) to acyl glycinate(s) is less than about 0.008; and
f. polyol(s) in a concentration of about 20 to 40.0 % by wt.
2. The composition according to claim 1 , wherein the composition is transparent.
3. The composition according to claim 1 or 2, wherein the composition is a foaming composition.
4. The composition according to any one of the preceding claims, further comprising C8 to C12 glucoside(s) in a total concentration of about 1 to 5 % by wt.
5. The composition according to any one of the preceding claims, further comprising C8 to C12 hydroxysultaine(s) in a total concentration of about 1 to 5 % by wt.
6. The composition according to any one of the preceding claims, wherein the
viscosity at 25 C is less than 40.0 mPas,
7. A packaged product for cleansing the skin comprising the composition according to any one of the preceding claims, contained in a mechanical pump foam dispenser wherein a foam is dispensed. 19
A method of cleansing and removing waxy makeup from the skin of a user comprising the steps of: a. dispensing as a foam an effective amount of the composition according to any one of claims 1 to 6, for removing oily makeup from wet skin;
b. applying the foam to the wet skin;
c. rubbing the foam on the wet skin for a time sufficient to disperse the oily makeup residing on the skin; and
d. rinsing the foamed composition and dispersed oily makeup from the skin.
A method according to claim 8, wherein the foam is dispensed by a non-aerosol foaming dispenser containing the composition according to any one of claim 1 to 6.
PCT/EP2013/067191 2012-08-23 2013-08-16 Mild foaming make-up remover composition WO2014029711A2 (en)

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EA201590177A EA027395B1 (en) 2012-08-23 2013-08-16 Aqueous liquid composition for cleansing the skin and method of removing waxy makeup
CN201380044248.1A CN104661636B (en) 2012-08-23 2013-08-16 Mild foaming make-up remover composition
BR112015003693A BR112015003693A2 (en) 2012-08-23 2013-08-16 aqueous liquid makeup for cleansing the skin, packaged product and method of cleansing and removing makeup.
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2547294A (en) * 2015-09-14 2017-08-16 Henkel Ag & Co Kgaa Cleaning compositions comprising biosurfactants in a foam dispenser
WO2020164087A1 (en) * 2019-02-15 2020-08-20 Beiersdorf Daily Chemical (Wuhan) Co. Ltd. A cleansing composition releasable as a shapeable foam
WO2020164086A1 (en) * 2019-02-15 2020-08-20 Beiersdorf Daily Chemical (Wuhan) Co. Ltd. A cleansing composition releasable in form of a stable foam
EP3621578B1 (en) 2017-05-10 2022-02-16 Unilever IP Holdings B.V. Low viscosity, high polyol self-foaming composition

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114728182B (en) 2019-11-20 2024-04-02 味之素株式会社 Detergent composition for foaming agent
WO2023065258A1 (en) * 2021-10-22 2023-04-27 Beiersdorf Ag A mild cleansing composition distributable from a pump foamer

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3709437A (en) 1968-09-23 1973-01-09 Hershel Earl Wright Method and device for producing foam
US3937364A (en) 1975-04-03 1976-02-10 Hershel Earl Wright Foam dispensing device
US4022351A (en) 1975-04-03 1977-05-10 Hershel Earl Wright Foam dispenser
US4147306A (en) 1977-09-28 1979-04-03 Bennett Robert S Foam producing apparatus
US4184615A (en) 1975-04-03 1980-01-22 Wright Hershel E Foam dispensing device
US4598862A (en) 1983-05-31 1986-07-08 The Dow Chemical Company Foam generating device and process
US4615467A (en) 1985-07-24 1986-10-07 Calmar, Inc. Liquid foam dispenser
FR2604622A1 (en) 1986-10-06 1988-04-08 Applied Chemical Research Corp Liquid shaving foam composition usable without any propellent gas in a compressible plastic flask
US5364031A (en) 1993-06-10 1994-11-15 The Procter & Gamble Company Foam dispensing nozzles and dispensers employing said nozzles
WO2008052956A1 (en) 2006-11-04 2008-05-08 Unilever Plc Make-up remover cosmetic compositions

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0246639B2 (en) * 1985-12-12 1990-10-16 Kao Corp SENJOZAISOSEIBUTSU
JP3556755B2 (en) * 1996-01-09 2004-08-25 株式会社ノエビア Makeup removal fee
JP3662513B2 (en) * 2000-04-27 2005-06-22 花王株式会社 Emulsified cosmetics
US7297717B2 (en) * 2000-04-27 2007-11-20 Kao Corporation Emulsion cosmetic
JP4551557B2 (en) * 2000-12-08 2010-09-29 阪本薬品工業株式会社 Skin cleanser composition
JP2003055131A (en) * 2001-06-06 2003-02-26 Ajinomoto Co Inc Cosmetic composition
JP2003267836A (en) * 2002-03-18 2003-09-25 Rohto Pharmaceut Co Ltd Gel-like cleansing cosmetic
US6812192B2 (en) * 2002-03-28 2004-11-02 L'oreal S.A. Foaming cosmetic compositions, uses for cleansing or make-up removal
JP4527655B2 (en) * 2004-11-30 2010-08-18 ライオン株式会社 Cleaner composition in former container
GB0804479D0 (en) * 2008-03-12 2008-04-16 Unilever Plc Make-up removal composition which provides good foam
DE102009034115A1 (en) * 2009-07-20 2011-01-27 Beiersdorf Ag Cosmetic preparation containing acylarginates
JP5700051B2 (en) * 2010-01-15 2015-04-15 味の素株式会社 N-acyl basic amino acid dispersion
DE102010007958A1 (en) * 2010-02-12 2011-08-18 Beiersdorf AG, 20253 Active ingredient combinations of acylarginates and quaternary ammonium compounds
DE102011107503A1 (en) * 2011-07-15 2012-03-01 Clariant International Ltd. Preparing acylglycinate compound useful in a composition, which is used as a surfactant in a cosmetic preparation, comprises reacting glycine with fatty acid chloride in water and in the presence of a basic alkali metal compound
JP2014218475A (en) * 2013-05-10 2014-11-20 ライオン株式会社 Antiperspirant composition
JP6337729B2 (en) * 2014-10-01 2018-06-06 日油株式会社 Hair cleaning composition

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3709437A (en) 1968-09-23 1973-01-09 Hershel Earl Wright Method and device for producing foam
US3937364A (en) 1975-04-03 1976-02-10 Hershel Earl Wright Foam dispensing device
US4022351A (en) 1975-04-03 1977-05-10 Hershel Earl Wright Foam dispenser
US4184615A (en) 1975-04-03 1980-01-22 Wright Hershel E Foam dispensing device
US4147306A (en) 1977-09-28 1979-04-03 Bennett Robert S Foam producing apparatus
US4598862A (en) 1983-05-31 1986-07-08 The Dow Chemical Company Foam generating device and process
US4615467A (en) 1985-07-24 1986-10-07 Calmar, Inc. Liquid foam dispenser
FR2604622A1 (en) 1986-10-06 1988-04-08 Applied Chemical Research Corp Liquid shaving foam composition usable without any propellent gas in a compressible plastic flask
US5364031A (en) 1993-06-10 1994-11-15 The Procter & Gamble Company Foam dispensing nozzles and dispensers employing said nozzles
WO2008052956A1 (en) 2006-11-04 2008-05-08 Unilever Plc Make-up remover cosmetic compositions

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2547294A (en) * 2015-09-14 2017-08-16 Henkel Ag & Co Kgaa Cleaning compositions comprising biosurfactants in a foam dispenser
EP3621578B1 (en) 2017-05-10 2022-02-16 Unilever IP Holdings B.V. Low viscosity, high polyol self-foaming composition
WO2020164087A1 (en) * 2019-02-15 2020-08-20 Beiersdorf Daily Chemical (Wuhan) Co. Ltd. A cleansing composition releasable as a shapeable foam
WO2020164086A1 (en) * 2019-02-15 2020-08-20 Beiersdorf Daily Chemical (Wuhan) Co. Ltd. A cleansing composition releasable in form of a stable foam

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