MX2015002280A - Mild foaming make-up remover composition. - Google Patents
Mild foaming make-up remover composition.Info
- Publication number
- MX2015002280A MX2015002280A MX2015002280A MX2015002280A MX2015002280A MX 2015002280 A MX2015002280 A MX 2015002280A MX 2015002280 A MX2015002280 A MX 2015002280A MX 2015002280 A MX2015002280 A MX 2015002280A MX 2015002280 A MX2015002280 A MX 2015002280A
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/046—Aerosols; Foams
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/345—Alcohols containing more than one hydroxy group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/361—Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/14—Preparations for removing make-up
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
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
MODERATE FOAM REMOVERING COMPOSITION
BACKGROUND OF THE INVENTION
1. Field of the invention
The invention concerns a cosmetic composition for removing makeup that is advantageously dispensed by a non-aerosol pump frothing dispenser as a durable foam.
2. History of the technique
An important segment of the cosmetics market are products that are used to remove makeup. The removal of eye shadow pigments, mascara, blush, lipstick and face powder is a daily problem for many women. The problem has been addressed through formulations which may include materials that operate 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 using a pump frothing dispenser have been introduced to the market to allow people to conveniently use the shower or bath, that is, with wet hands, and dispense the product as foam for quick action. on the skin without dripping.
W02008052956 published May 8, 2008, for Kobayashi et al. , describes a cleaning composition including a mixture of tri-ester (s) of non-saccharide polyhydric alcohol fatty acids and
tetraester (s) of fatty acids of saccharide alcohols in a specific ratio and mixed with oil that removes make-up under humid conditions, such as with wet hands without the problem of phase separation and committed make-up removal efficiency.
Surprisingly, a formulation including a mixture of an acyl glycinate (s) and acyl argininate (s) in a specific ratio range, mixed with polyol (s) and water, was found to produce considerable and lasting foam when dispenses in moist skin and also clean and with the expectation of moisturizing the skin, compared with makeup removers. Additionally, 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 mechanical hob pump to be dispensed directly onto the hands. Preferably, the pump is placed in a stable position, so that the hand or forearm can be used to squeeze the pump and dispense the product. This results in a more hygienic cleaning process. In addition, initial dilution with water is not required because the foam can be easily distributed on the skin before rinsing. The inventive product is preferably transparent. Transparency is defined here 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 a liquid, aqueous, preferably transparent, preferably foaming, composition for cleansing the skin, including but not limited to:
to. soap or soaps of C8 to C18 in a total concentration range of about 0.1 to 10% by weight;
b. acyl glycinate (s) from C10 to C14 in a total concentration range of about 5 to 25% by weight;
c. acyl arginine (s) from C10 to C14 in a total concentration range of about 0.01 to 0.1% by weight;
d. greater than about 30% by weight of water;
and. wherein the ratio of acyl arginine (s) to acyl glycinate (s) is less than about 0.008; Y
F. polyol (s) in a concentration of about 20 to 40.0% by weight.
In another preferred embodiment is a packaged skin cleaning product comprising the above composition contained in a mechanical pump foam dispenser, where a foam is dispensed.
In a further preferred embodiment is a method for cleaning and removing waxy make-up from a user's skin including, but not limited to, the steps of:
to. dispensing as a foam, an effective amount of the above composition to remove oily makeup from wet skin; b. apply the foam to damp skin;
c. rubbing the foam on damp skin for a sufficient time to disperse the oily makeup that resides on the skin; and d. Rinse the foamed composition and oily makeup dispersed 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 liquid composition, preferably transparent, preferably foaming, for cleaning the skin, including but not limited to:
to. soap or soaps of C8 to C18 in a total concentration range of about 0.1 to 10% by weight; preferably 0.1 to 5.0 and more preferably 0.1 to 1.0;
b. acyl glycinate (s) from C10 to C14 in a total concentration range of about 5 to 25% by weight; preferably 5.0 to 15.0 and more preferably 10.0 to 15.0;
c. acyl arginine (s) from C10 to C14 in a total concentration range of about 0.01 to 0.1% by weight; preferably 0.01 to 0.08 and more preferably 0.02 to 0.08;
d. greater than about 30% by weight of water; preferably greater than 40.0 and more preferably greater than 50.0;
and. 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; Y
F. polyol (s) in a concentration of about 20 to 40.0% by weight, 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 clear foaming liquid composition for cleaning the skin.
Advantageously, the inventive composition further includes C8 to C12 glucoside (s) in a total concentration of about 1 to 5% by weight, preferably about 1.0 to 4.0 and more preferably about 1.0 to 3.0. Preferably, C8 to C12 hydroxysultaine (s) are also included in a total concentration of about 1 to 5% by weight, 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, there is a packaged product for cleaning the skin comprising the above composition contained in a mechanical pump foam dispenser, where a foam is dispensed.
In a further preferred embodiment, a method is found for cleaning and removing waxy makeup from a user's skin including but not limited to the steps of:
to. dispensing as a foam an effective amount of the above composition to remove oily makeup from wet skin; b. apply the foam to damp skin;
c. rubbing the foam on damp skin for a sufficient time to disperse the oily makeup that resides on the skin; and d. Rinse the foamed composition and oily makeup dispersed from the skin.
Soaps
Normal C8-C18 alkyl carboxylic acid soaps are used for the invention. Preferably the soap or carboxylic acid soaps, such as lauric (C12), myristic (C14), palmitic (C16) or stearic (18) soaps are used alone or in combination. Advantageously, the soap (s) are used at levels as low as 0.1% by weight and at levels as high as 1, 5 or 10% by weight.
Synthetic anionic surfactants
One or more C10-C14 acyl glycinate (s) are used in the inventive composition. It is preferably used at levels as low as 5 or 10% by weight, and at levels as high as 15, 20 or 25% by weight. The inventive composition also contains one or more acyl arginases having the following formula, wherein R can have values of 10 to 14 and of
Preferably represents an unbranched alkyl chain of 11 (lauroyl arginate).
Other anionic detergent actives, which may be used in the invention, may be aliphatic sulfonates, such as primary alkane sulphonate (e.g., C8-C22), primary alkane disulfonate (e.g., C8-C22), alkene sulfonate of C8-C22, C8-C22 hydroxyalkane sulphonate or alkyl glyceryl ether slfonate (AGS); or aromatic sulfonates, such as alkyl benzene sulfonate. The anionic can also be an alkyl sulfate (for example, C12-C18 alkyl sulfate) or alkyl ether sulfate (including alkyl glyceryl ether sulfates). Among the alkyl ether sulfates are those having the formula:
R0 (CH2CH2O) nS03M
wherein R is an alkyl or alkenyl having 8 to 18 carbons, preferably 12 to 18 carbons, n has an average value of more than 1.0,
preferably greater than 3; and M is a solubilizing cation, such as sodium, potassium, ammonium or substituted ammonium. Sodium ammonium lauryl ether sulfates are preferred.
The anionic may also be alkyl sulfosuccinates (including mono- and dialkyl, eg, C6-C22 sulfosuccinates), alkyl and acyl taurates, alkyl and acyl sarcosinates, sulphoacetates, C8-C22 alkyl phosphates and phosphates, alkyl phosphate esters and esters of alkoxyl alkyl phosphate, acyl lactates, C8-C22 monoalkyl succinates and maleates, sulfoacetates, alkyl glucosides and acyl isethionates, and the like.
The sulfosuccinates can be monoalkyl sulfosuccinates having the formula:
R402CCH2CH (S03M) CO2M; Y
amide-MA sulfosuccinates of the formula;
R4C0NHCH2CH2O2CCH2CH (S03M) C02M,
wherein R 4 varies from C 8 -C 22 alkyl and M is a solubilizing cation.
Sarcosinates are usually indicated by the formula:
R1C0N (CH3) CH2C02M,
wherein R1 varies from C8-C20 alkyl and M is a solubilizing cation.
Tauratos are generally identified by the formula
R2CONR3CH2CH2S03M
wherein R 2 varies from C 8 -C 20 alkyl, R 3 varies from C 1 -C 4 alkyl and M is a solubilizing cation.
Polyols
One or more polyols are present in compositions of this invention. These polyols can be monomeric or polymeric. The monomeric polyols can have from 1 to 20 carbon atoms and from 2 to 10 hydroxyl. Exemplary monomeric polyols include glycerin, propylene glycol; 1,4-butane diol; 1,3-butane diol; 1,2-butane diol; 1, 6-hexanediol, 1,2-hexanediol, 3-methyl-1,3-butane diol, 2-methyl-1,3-propane diol, sorbitol and mixtures thereof and the like. Glycerin, propylene glycol and 1,3-butane diol are particularly preferred.
Polymeric polyols are illustrated by polypropylene glycol, polyethylene glycol, dipropylene glycol, diglycerol, polyglycerol, trimethylene glycol, dipentaerythritol and combinations thereof and the like.
Non-ionic and amphoteric surfactants
A variety of non-ionic and amphoteric surfactants may be employed as optional additional components of the present invention. The nonionic surfactants are ordinarily based on a hydrophobic 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
about 12 carbon atoms in the alkyl chain, sorbitan and mixtures thereof. These hydrophobes will ordinarily be condensed with a hydrophilic unit, in particular 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 sorbitan POE-20 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 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, for example, lauryl hydroxy sultaine, cocamidopropyl betaine, cocoamido sultaine, dodecyl dimethyl betaine, cetyl dimethyl betaine and combinations thereof and the like.
The amounts of the nonionic surfactants can each vary from about 0.01 to about 10%, preferably from about 0.2 to about 5%, optimally from about 0.3 to about 7% by weight of the composition. The amounts of amphoteric surfactants can
each varying 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.
Various components
Water is preferably present in an amount of more than about 30% by weight, preferably more than 40.0% by weight and more preferably more than 50.0% by weight. The amount of water is preferably less than 75% by weight. Water is preferably present in an amount of about 30% by weight to 75% by weight.
The talkers will usually also be incorporated into the inventive formulations. Representative materials include phenoxyethanol, methyl paraben, propyl paraben, salts of ethendiamine tetraacetate (EDTA), benzyl alcohol, iodopropynyl butyl carbamate, DMDM hydantoin, caprylyl glycol and combinations thereof and the like. The amounts of these materials can vary 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 achieve their respective functions. Typical promotional ingredients include vitamins, such as retinyl palmitate, tocopherol acetate and niacinamide. Other ingredients
Promotions include conjugated linoleic acid, ceramides, pentapeptides and combinations thereof.
Compositions of the present invention are preferably 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 insoluble in water means any emollient having a solubility in distilled water at 25 ° C less than about 1 gm per 100 ml, more preferably less than about 0.1 gm per 100 mi. Without 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-11 +, spindle No. LV1, using 60 rpm and 1 min of measurement time.
Non-aerosol foam dispenser
A preferred embodiment of the cleaning product according to this invention is a non-aerosol skimmer dispenser containing the inventive composition. The inventive composition is dispensed as a foam and produces a copious and durable foam in contact with moist 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 of the container to the dispensing head. The foam is created by requiring the composition to pass through a screening material which may be a porous substance, such as a sintered material, a wire mesh screen (plastic or metal) or similar structures. Preferably, two screens are used.
Suitable mechanical dispensers are described in U.S. Pat. 3,709,437 (Wright), U.S. Patent No. 3,937,364 (Wright), U.S. Patent No. 4,022,351 (Wright), U.S. Patent No. 4, 147, 306 (Bennett), U.S. Patent No. 4, 184,615 (Wright), US Patent no. 4,598,862 (Rice), U.S. Patent No. 4,615,467 (Grogan et al.), And US Patent no. 5,364,031 (Tamiguchi et al.): All of these patents are incorporated herein by reference.
A preferred skimmer is the pump foaming head F5L manufactured by Daiwa Corporation located in (Tokyo, Japan). This frother 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: Mesh 255 (Top) / 200 (Bottom) Air / liquid ratio: 9.5 / 1
Volume by 1 pulse: 0.95 g
Other suitable skimmers may include shrink skimmers. Compression skimmer packages
they are well known as exemplified by the descriptions in the following patents which are incorporated herein by reference. U.S. Patent Nos: 3,709,437, Wright, issued January 9, 1973; 3,937,364, Wright, issued February 10, 1976; 4,022,351; Wright, issued on May 10, 1977; 4, 147, 306, Bennett, issued April 3, 1979; 4, 184, 615, Wright, issued January 22, 1980; 4,598,862, Rice, issued July 8, 1986; and 4,615,467, Grogan et al., issued October 7, 1986; and French Patent 2,604,622, Verhulst, published April 8, 1988.
When shrinking skimmers are used, the composition is placed in the container reservoir (plastic compression bottle). Compressing the container by hand forces the composition through a foaming head, or other foam producing medium, where the composition is mixed with air and then through a homogenizing medium that makes the foam more homogeneous and controls the consistency of the foam. The foam is then discharged as a non-pressurized, uniform aerated foam.
The invention will now be described in greater detail by means of the following non-limiting example. The example is for illustrative purposes only and is not intended to limit the invention in any way. The physical test methods are described below:
Except in the operational and comparative examples, or where otherwise explicitly indicated, all figures in this description that indicate quantities or proportions of materials or conditions of
reaction, physical properties of materials and / or use are to be understood as modified by the word "approximately".
Where used in the specification, the term "comprises" is intended to include the presence of features, integers, steps, declared components, but not to exclude 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 the clarity, foam stability on contact with a wet substrate and on the basis of dry makeup and ease of pumping foam with the F5L foaming pump to
-5 ° C described above.
OI or I heard
Table 1
Ro I?
OI or OI or OI
*% by weight on active basis
(1) - (4) see procedures below
< or
Based on the results reported in Table 1, it is evident that the best foam stability under both wet and dry conditions and the 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 to 80 ° C with shaking. If it dissolves after 10 minutes at 80 ° C, then the rating is "OK". If there are visible insoluble materials remaining after 10 minutes, then the rating is "NG".
(2) Stability of foam on a wet surface
1. Wet a paper towel evenly with water without throwing away the water.
2. Dispense approximately 0.7 g of the sample from the F5L pump frother on the wet towel.
3. Observe the foam properties after 15 min under ambient conditions in air at approx. 20 ° C (RT) and 50% RH.
4. Graduate foam stability as follows:
+ TOTAL FOAM COLLAPSE
++ SOMETHING OF FOAM COLLAPSE
+++ VERY LITTLE FOAM COLLAPSE
(3) Stability of dry foundation based foams
1. Apply 0.2 g of base (Shiseido MAQUILLAGE Lasting Liquid UV, Ocher 10 All Season Type available from Shiseido, Tokyo, Japan) in a homogeneous square pattern of 1.5 cm x 15 cm on a polypropylene plastic board.
2. Allow to dry for 10 min under ambient conditions in air at approx. 20 C (RT) and 50% RH.
3. Dispense approximately 0.7 g of samples from the F5L pump skimmer to the dry base.
4. Observe the foam stability after 15 min under ambient conditions in air at approx. 20 ° C (RT) and 50% RH.
5. Rate the foam stability as follows:
+ TOTAL FOAM COLLAPSE
++ SOMETHING OF FOAM COLLAPSE
+++ VERY LITTLE FOAM COLLAPSE
(4) Ease of foam dispensing from the pump
Fill a container with the liquid cleaning product while leaving an air space. Seal with a F6L pump foaming head manufactured by Daiwa Corporation (Tokyo, Japan). Press the pump and observe if foam is dispensed. If foam is dispensed, qualify the dispensing facility of the pump as "OK". If it is not dispensed (for example, only a liquid is dispensed), qualify the facility to foam the pump as "NG".
(5) Moistening test:
1. Mount a panel of trained people.
2. Put approximately 3 g of a test sample on the right forearm of each panelist.
3. Rinse under running water at room temperature for a few minutes.
4. Dry with a towel, then qualify the moisturizing sensation using a maximum score of 5 points per panelist, then add all the qualifications.
5. Repeat using approximately 3 g of the comparative test sample on the left forearm of each panelist.
6. Alternatively, a suitable instrumental method can be used to compare the skin wetness between the samples. All instrumental evaluations will be taken following an acclimatization period of 30 minutes. The interior humidity and temperature data will be recorded and included in the final report. Instrumental measurements can be taken at some or all of the following points in time: 0, 1, 2, 4, 6, 8 and 24 hours after product application.
The instruments to be used with this protocol may include, but are not limited to, ServoMed Evaporimeter with EP1 or EP2 probe (SeroMed AB, Stockholm, Sweden), Corneometer CM820 (COURAGE + KHAZAK Electronic GmbH, Cologne, Germany), the hygrometer Skicon skin with the MT-8C probe (IBS CO., LTD., Shizuoka-ken, Japan), and the humidity tester (STR - School &
Science Technology Resources, Scotts Vallcy, Ca). The ambient temperature will be maintained at 68 ° F to 77 ° F (20 ° C to 25 ° C) and 30% to 40% relative humidity. Moistening will be defined as an average change from the baseline (visual dryness or skin hydration).
(6) Procedure to prepare the examples illustrated in Table 1:
1. Dissolve Amisafe in Amilite GCK-12K at 80 ° C (Phase 1) until the solution is clear.
2. Mix water and glycerin at 80 ° C until it was homogenous (Phase 2).
3. Add Phase 1 to Phase 2 at 80 ° C and mix.
4. Add NONSOUL LK-30 at 80 ° C and mix.
5. Add Amphitol, Mydol12 and mix well.
6. Cool to 35 ° C.
(7) Turbidity
For the purposes of this invention, the acceptability of formulation transparency or clarity can be measured qualitatively and quantitatively using a visual method of turbidity determination and a turbidimeter, respectively. Briefly, the visual method involves observing through a determined stretch of the formulation a visual objective and determining whether the visual objective is readable or recognizable. This objective can be a straight line, a set of parallel lines, a number or a letter printed on white paper.
Place the test formulation in a glass laboratory beaker, so that the height of the bottom of the lab beaker to the top surface of the formulation is four inches. Make sure the formulation is free of bubbles. Place the piece of paper with the visual objective under the laboratory glass. Look through the upper surface of the formulation to the visual objective. If the visual objective appears similar to the original, the formulation is of acceptable clarity and receives a "pass" rating. If the visual objective seems significantly nebulous, or is out of focus, compared to the original objective, the formulation is of unacceptable clarity and receives a "failure" rating.
The turbidity can be determined quantitatively by a Turbidimeter, model DRT-100D, manufactured by Shaban Manufacturing Inc, H.F. Instruments Division using a sample tube 28 mm in diameter by 91 mm in length with a flat bottom. It is expected that samples that receive a "pass" rating from the visual method will have a turbidity measurement less than or equal to 105 NTU's (Nephelometric Turbidity Units). Samples that receive a "failure" rating of the visual method will have a turbidity measurement greater than 105 NUT's.
The description and examples above 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 (9)
1. A liquid, aqueous composition for cleaning the skin, comprising: to. soap or soaps of C8 to C18 in a total concentration range of about 0.1 to 10% by weight; b. acyl glycinate (s) from C10 to C14 in a total concentration range of about 5 to 25% by weight; c. acyl arginine (s) from C10 to C14 in a total concentration range of about 0.01 to 0.1% by weight; d. greater than about 30% by weight of water; and. wherein the ratio of acyl arginine (s) to acyl glycinate (s) is less than about 0.008; Y F. polyol (s) in a concentration of about 20 to 40.0% by weight. b. acyl glycinate (s) from C10 to C14 in a total concentration range of about 5 to 25% by weight; c. acyl arginine (s) from C10 to C14 in a total concentration range of about 0.01 to 0.1% by weight; d. greater than about 30% by weight of water; and. wherein the ratio of acyl arginine (s) to acyl glycinate (s) is less than about 0.008; Y F. polyol (s) in a concentration of about 20 to 40.0% by weight.
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 of the preceding claims, further comprising C8 to C12 glucoside (s) in a total concentration of about 1 to 5% by weight.
5. The composition according to any of the preceding claims, further comprising C8 to C12 hydroxysultaine (s) in a total concentration of 1 to 5% by weight.
6. The composition according to any of the preceding claims, wherein the viscosity at 25 ° C is less than 40.09 mPas.
7. A packaged product for cleaning the skin comprising the composition according to any of the preceding claims, contained in a mechanical pump foam dispenser, wherein a foam is dispensed.
8. A method for cleaning and removing waxy make-up from a user's skin comprising the steps of: to. dispensing as a foam an effective amount of the composition according to any of claims 1 to 6, to remove oily makeup from wet skin; b. apply the foam to damp skin; c. rubbing the foam on damp skin for a sufficient time to disperse the oily makeup that resides on the skin; Y d. Rinse the foamed composition and oily makeup dispersed from the skin.
9. A method according to claim 8, wherein the foam is dispensed by a non-aerosol skimmer dispenser containing the composition according to any of claims 1 to 6.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB201215054A GB201215054D0 (en) | 2012-08-23 | 2012-08-23 | Mild foaming make-up remover composition |
PCT/EP2013/067191 WO2014029711A2 (en) | 2012-08-23 | 2013-08-16 | Mild foaming make-up remover composition |
Publications (2)
Publication Number | Publication Date |
---|---|
MX2015002280A true MX2015002280A (en) | 2015-08-20 |
MX352365B MX352365B (en) | 2017-11-22 |
Family
ID=47045303
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2015002280A MX352365B (en) | 2012-08-23 | 2013-08-16 | Mild foaming make-up remover composition. |
Country Status (8)
Country | Link |
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JP (1) | JP6333253B2 (en) |
CN (1) | CN104661636B (en) |
BR (1) | BR112015003693A2 (en) |
EA (1) | EA027395B1 (en) |
GB (1) | GB201215054D0 (en) |
MX (1) | MX352365B (en) |
TW (1) | TWI586372B (en) |
WO (1) | WO2014029711A2 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102015217502A1 (en) * | 2015-09-14 | 2017-03-16 | Henkel Ag & Co. Kgaa | Cleaning compositions with biosurfactants in a foam dispenser |
JP2020519572A (en) * | 2017-05-10 | 2020-07-02 | ユニリーバー・ナームローゼ・ベンノートシヤープ | 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 |
JPWO2021100812A1 (en) | 2019-11-20 | 2021-05-27 | ||
WO2023065258A1 (en) * | 2021-10-22 | 2023-04-27 | Beiersdorf Ag | A mild cleansing composition distributable from a pump foamer |
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US4022351A (en) | 1975-04-03 | 1977-05-10 | Hershel Earl Wright | Foam dispenser |
US3937364A (en) | 1975-04-03 | 1976-02-10 | Hershel Earl Wright | 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 |
JPH0246639B2 (en) * | 1985-12-12 | 1990-10-16 | Kao Corp | SENJOZAISOSEIBUTSU |
FR2604622B1 (en) | 1986-10-06 | 1990-12-14 | Applied Chemical Research Corp | LIQUID COMPOSITION FOR SHAVING FOAM FOR USE WITHOUT PROPELLANT GAS IN A BOTTLE OF COMPRESSIBLE PLASTIC MATERIAL |
US5364031A (en) | 1993-06-10 | 1994-11-15 | The Procter & Gamble Company | Foam dispensing nozzles and dispensers employing said nozzles |
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 |
GB0621993D0 (en) | 2006-11-04 | 2006-12-13 | Unilever Plc | Make-up remover cosmetic compositions |
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 |
WO2011088327A2 (en) * | 2010-01-15 | 2011-07-21 | Ajinomoto Co., Inc. | 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 |
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2012
- 2012-08-23 GB GB201215054A patent/GB201215054D0/en not_active Ceased
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2013
- 2013-08-14 TW TW102129168A patent/TWI586372B/en not_active IP Right Cessation
- 2013-08-16 EA EA201590177A patent/EA027395B1/en not_active IP Right Cessation
- 2013-08-16 CN CN201380044248.1A patent/CN104661636B/en active Active
- 2013-08-16 JP JP2015527873A patent/JP6333253B2/en active Active
- 2013-08-16 WO PCT/EP2013/067191 patent/WO2014029711A2/en active Application Filing
- 2013-08-16 MX MX2015002280A patent/MX352365B/en active IP Right Grant
- 2013-08-16 BR BR112015003693A patent/BR112015003693A2/en not_active Application Discontinuation
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JP2015526451A (en) | 2015-09-10 |
TWI586372B (en) | 2017-06-11 |
EA027395B1 (en) | 2017-07-31 |
EA201590177A1 (en) | 2015-07-30 |
WO2014029711A3 (en) | 2014-09-12 |
MX352365B (en) | 2017-11-22 |
BR112015003693A2 (en) | 2017-07-04 |
CN104661636A (en) | 2015-05-27 |
WO2014029711A2 (en) | 2014-02-27 |
GB201215054D0 (en) | 2012-10-10 |
TW201408331A (en) | 2014-03-01 |
CN104661636B (en) | 2017-05-10 |
JP6333253B2 (en) | 2018-05-30 |
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