WO2013170419A1 - Emulsifier composition and the use thereof - Google Patents
Emulsifier composition and the use thereof Download PDFInfo
- Publication number
- WO2013170419A1 WO2013170419A1 PCT/CN2012/075451 CN2012075451W WO2013170419A1 WO 2013170419 A1 WO2013170419 A1 WO 2013170419A1 CN 2012075451 W CN2012075451 W CN 2012075451W WO 2013170419 A1 WO2013170419 A1 WO 2013170419A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- oil
- emulsifier
- water
- acid
- component
- Prior art date
- Legal status (The legal status 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 status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/54—Silicon compounds
-
- 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
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
- A61K8/064—Water-in-oil emulsions, e.g. Water-in-silicone emulsions
-
- 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
- A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups
-
- 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
- A61K8/42—Amides
-
- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
- A61K8/894—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/017—Mixtures of compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/22—Amides or hydrazides
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/34—Higher-molecular-weight carboxylic acid esters
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/10—General cosmetic use
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/596—Mixtures of surface active compounds
Definitions
- the present invention relates to an emulsifier composition and the use thereof in the preparation of water-in-oil emulsions.
- Water-in-oil emulsions especially high inner phase content water-in-oil emulsions are well known for their special skin sensory, water resistance and skin moisturizing properties. At present, they are produced by slowly adding the inner water phase into the oil phase containing an emulsifier under stirring. However, during this process, the water phase must be added "slowly” such that all the water can be steadily encapsulated as the inner phase into the oil phase. If all the water phase and all the oil phase are directly mixed and homogenized, a water-in-oil emulsion will not be available, even the time for homogenization is extended.
- the present invention provides an emulsifier composition which can improve the process for the preparation of a water-in-oil emulsion.
- the present invention further provides a water-in-oil emulsion comprising the emulsifier composition of the present invention.
- the present invention further provides a process for the preparation of the water-in-oil emulsion of the present invention.
- a water-in-oil emulsion can be obtained through simply mixing the inner and outer phases, which is much more convenient than conventional processes.
- the emulsifier composition of the present invention comprises
- R 1 is an aliphatic hydrocarbyl group having 7-21 carbon atoms
- R 2 is a hydrocarbylene group having 1-4 carbon atoms
- R 3 and R 4 are independently a hydrocarbyl group having 1-4 carbon atoms.
- Component a) constitutes 50-99.5%, more preferably 80-99%
- Component b) constitutes 0.5-50%, more preferably 1-20%
- Component a) is selected from surfactants having an HLB value less than 12, preferably an HLB value from 2-8, calculated according to the Davies method.
- Component a) has hydrophilic groups selected from polyoxyethylene groups, polyoxypropylene groups, polyglycerol groups, poly oxy ethylene sorbitan groups.
- Component a) can be one or more selected from the following three types: The first type: an emulsifier having a molecular chain structure of polysiloxane + a hydrophilic group + an alkyl, which comprises a block copolymer emulsifier of polysiloxane, a polyetherpolyol and a C C 22 aliphatic alkane connected by covalent bonds, an emulsifier with a polysiloxane chain as the main chain, and polyetherpolyol and C 1 -C 22 aliphatic alkyl as side groups which are respectively connected to the main chain of polysiloxane by covalent bonds, and an emulsifier with a polysiloxane chain as the main chain, C C 22 aliphatic alkyl modified polyetherpol
- the second type an emulsifier having a molecular chain structure of polysiloxane + a hydrophilic group, which emulsifier comprises a block copolymer emulsifier with polysiloxane and a polyetherpolyol connected by covalent bonds, an emulsifier with a polysiloxane chain as the main chain, and polyetherpolyol as side groups connected to the main chain of polysiloxane by covalent bonds; preferably polyoxy ethylene polydimethylsiloxane, polyglycerol polydimethylsiloxane, and more preferably bis-PEG/PPG- 14/14 polydimethylsiloxane (for example the one supplied under the trade name of ABIL ® EM97 by Evonik Goldschmidt GmbH); and
- the third type an ester emulsifier formed by a polyetherpolyol or a polyol of a non-linear structure or a linear structure, via its hydroxyl group, with a C 1 -C 22 fatty acid, or an ether emulsifier formed by a polyetherpolyol or a polyol, via its hydroxyl group, with a C C 2 2 fatty alcohol, which comprises a polyoxyethylene fatty acid ester, a polyoxyethylene alkyl ether, a mono- or poly- glycerol fatty acid ester, a mono- or poly- glycerol alkyl ether, preferably diisostearyl polyglyceryl- 3 dimer dilinoleate (for example the one supplied under the trade name of ISOLAN ® GPS by Evonik Goldschmidt GmbH), polyglyceryl-4 diisostearate/polyhydroxystearate/sebacate (for example the one supplied under the trade name ISOLAN ® GPS by
- Goldschmidt GmbH can have the following structure:
- R 1 is an alkyl in the structure of the amido amine of Component b).
- R 1 is a straight or branched alkyl having 15-21 carbon atoms.
- R is an alkylene in the structure of the amido amine of Component b).
- R 3 and R 4 are independently an alkyl in the structure of the amido amine of Component b).
- amido amine is N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl amine
- the fatty acid of Component b) is not limited to straight or branched, saturated or unsaturated fatty acids.
- the fatty acid of Component b) is selected from lauric acid, isostearic acid, stearic acid, myristic acid, oleic acid and palmitic acid.
- the equivalent ratio of the fatty acid to the amido amine is 0.5-5: 1, more preferably 0.9-1.5: 1, particularly 1 :1.
- the emulsifier of the present invention further comprises: c) at least one metal salt of a fatty acid, the fatty acid salt having 8-22 carbon atoms.
- Component a) constitutes 30-90%, more preferably 40-80%, Component b) constitutes 0.5-10%, more preferably 1-8%,
- Component c) constitutes 5-65%, more preferably 20-50%,
- the fatty acid of Component c) is not limited to straight or branched, saturated or unsaturated fatty acids.
- the fatty acid of Component c) is selected from lauric acid, isostearic acid, stearic acid, myristic acid, oleic acid and palmitic acid.
- the metal of Component c) is selected from Ba, Mg, Al, Zn, and Ca.
- the present invention furthers provides a water-in-oil emulsion comprising:
- the oil phase constitutes 15-65%, more preferably 20-50%
- the water phase constitutes 30-80%, more preferably 50-80%
- the emulsifier composition constitutes 1-10%, more preferably 2-5%, based on the total weight of the emulsion.
- the oil phase is one or more selected from siloxanes, fatty hydrocarbons, alcohols, esters and ethers.
- the oil phase is one or more selected from polydimethylsiloxanes, cyclomethicones, aryl- or alkyl- or alkoxy- substituted polydimethylsiloxanes or cyclomethicones, methyl laurate, n- hexyl laurate, 2-ethylhexyl laurate, methyl stearate, isopropyl stearate, n- butyl stearate, octyl stearate, isooctyl stearate, 2-hexyldecyl stearate, steryl heptanoate, methyl oleate, isopropyl oleate, decyl oleate, oleyl oleate, erucyl oleate, decyl linoleate, stearyl heptanoate, isopropyl myristate, myristyl myristate, methyl
- the water-in-oil emulsion comprises an optional water miscible alcohol, preferably the water miscible alcohol is one or more selected from monohydric alcohols, diols or triols, more preferably the water miscible alcohol is one or more selected from 1 ,2-proplyene glycol, 1,3-propylene glycol and glycerin.
- the water miscible alcohol is one or more selected from monohydric alcohols, diols or triols, more preferably the water miscible alcohol is one or more selected from 1 ,2-proplyene glycol, 1,3-propylene glycol and glycerin.
- the water-in-oil emulsion further comprises at least one water soluble electrolyte, preferably the electrolyte is one or more selected from sodium chloride, potassium chloride, sodium citrate, sodium lactate, magnesium sulfate, calcium chloride and salts of amino acids.
- the electrolyte is one or more selected from sodium chloride, potassium chloride, sodium citrate, sodium lactate, magnesium sulfate, calcium chloride and salts of amino acids.
- the water-in-oil emulsion further comprises at least one water soluble functional additive for cosmetics, for example, those supplied by Evonik Industries under the trade names TEGO ® COSMO C 100, LACTIL ® and TEGO ® NATURAL BETAIN.
- at least one water soluble functional additive for cosmetics for example, those supplied by Evonik Industries under the trade names TEGO ® COSMO C 100, LACTIL ® and TEGO ® NATURAL BETAIN.
- the present invention further provides a process for the preparation of the water-in-oil emulsion of the present invention, comprising:
- Step 1) is carried out at 70-120°C, more preferably at 80- 110°C.
- Step 2) is carried out at 70-100°C, more preferably at 80- 90°C.
- Step 3 is carried out at 70-100°C, more preferably at 80- 90°C.
- Step 3 is carried out at a stirring speed of 1000-10000 rpm, more preferably at a stirring speed of 1500-7500 rpm.
- water-in-oil emulsion of the present invention other components generally used in cosmetics, pharmaceuticals, and so on can be arbitrarily incorporated, as necessary, within the range that the effect of the present invention is not undermined.
- UV protection agents examples thereof include UV protection agents, moisturizers, water- soluble polymers, thickeners, coating agents, metal ion sequestering agents, lower alcohols, polyhydric alcohols, pH adjusters, antioxidants, antioxidant aids, and perfumes.
- water-in-oil emulsion of the present invention is not limited in particular, and the water-in-oil emulsion can be applied in cosmetic products such as pre-makeup, foundation, cheek color, eye shadow, eye liner, sunscreen products, and body-care cosmetics.
- Group A mainly the oil phase and emulsifier composition
- the components of Group A were mixed at 105°C until all the solid ingredients were dissolved completely. Then the mixture of Group A was cooled down to 80°C.
- Group B (mainly the water phase) were mixed at 80°C until all the solid ingredients were dissolved completely. Then both the mixtures of Groups A and B were mixed immediately at 80°C and homogenized for 2-5 minutes at a stirring speed of 1000-10000 rpm.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Emergency Medicine (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Dispersion Chemistry (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Description
EMULSIFIER COMPOSITION AND THE USE THEREOF Field of the invention
The present invention relates to an emulsifier composition and the use thereof in the preparation of water-in-oil emulsions.
Background
Water-in-oil emulsions, especially high inner phase content water-in-oil emulsions are well known for their special skin sensory, water resistance and skin moisturizing properties. At present, they are produced by slowly adding the inner water phase into the oil phase containing an emulsifier under stirring. However, during this process, the water phase must be added "slowly" such that all the water can be steadily encapsulated as the inner phase into the oil phase. If all the water phase and all the oil phase are directly mixed and homogenized, a water-in-oil emulsion will not be available, even the time for homogenization is extended. The above mentioned process is much different from normal processes for the preparation of oil-in- water emulsions named "one step emulsification" wherein all the water and oil phase are immediately mixed and then homogenized. As oil-in-water emulsions are easily realized, cosmetic manufactures will prefer to use oil-in-water emulsions. To some extent, the application and promotion of water-in-oil emulsions are limited by the current inconvenient process for preparing such emulsions.
Summary of the invention
The present invention provides an emulsifier composition which can improve the process for the preparation of a water-in-oil emulsion.
The present invention further provides a water-in-oil emulsion comprising the emulsifier composition of the present invention.
The present invention further provides a process for the preparation of the water-in-oil emulsion of the present invention.
By the use of the emulsifier composition of the present invention, a water-in-oil emulsion can be obtained through simply mixing the inner and outer phases, which is much more convenient than conventional processes.
Detailed description of the invention
The emulsifier composition of the present invention comprises
a) at least one water-in-oil emulsifier;
b) at least one fatty acid salt of an amido amine or the precursor mixture thereof consisting of the corresponding fatty acid and the amido amine, the fatty acid having 8-22 carbon atoms,
the amido amine having the following structure, R1-C(0)-NH-R2-N(R3)(R4); wherein
R1 is an aliphatic hydrocarbyl group having 7-21 carbon atoms;
R2 is a hydrocarbylene group having 1-4 carbon atoms;
R3 and R4 are independently a hydrocarbyl group having 1-4 carbon atoms.
Preferably, Component a) constitutes 50-99.5%, more preferably 80-99%, Component b) constitutes 0.5-50%, more preferably 1-20%,
based on the total weight of the emulsifier composition.
Preferably, Component a) is selected from surfactants having an HLB value less than 12, preferably an HLB value from 2-8, calculated according to the Davies method.
Preferably, Component a) has hydrophilic groups selected from polyoxyethylene groups, polyoxypropylene groups, polyglycerol groups, poly oxy ethylene sorbitan groups. Preferably, Component a) can be one or more selected from the following three types:
The first type: an emulsifier having a molecular chain structure of polysiloxane + a hydrophilic group + an alkyl, which comprises a block copolymer emulsifier of polysiloxane, a polyetherpolyol and a C C22 aliphatic alkane connected by covalent bonds, an emulsifier with a polysiloxane chain as the main chain, and polyetherpolyol and C1-C22 aliphatic alkyl as side groups which are respectively connected to the main chain of polysiloxane by covalent bonds, and an emulsifier with a polysiloxane chain as the main chain, C C22 aliphatic alkyl modified polyetherpolyol as side groups which are connected to the polysiloxane chain by covalent bonds; preferably C6-C2o alkyl-copolymerized polyoxyethene polydimethylsiloxane, and more preferably cetyl PEG/PPG- 10/1 polydimethylsiloxane (for example the one supplied under the trade name of ABIL® EM90 or ABIL® EM 180 by Evonik Goldschmidt GmbH);
The second type: an emulsifier having a molecular chain structure of polysiloxane + a hydrophilic group, which emulsifier comprises a block copolymer emulsifier with polysiloxane and a polyetherpolyol connected by covalent bonds, an emulsifier with a polysiloxane chain as the main chain, and polyetherpolyol as side groups connected to the main chain of polysiloxane by covalent bonds; preferably polyoxy ethylene polydimethylsiloxane, polyglycerol polydimethylsiloxane, and more preferably bis-PEG/PPG- 14/14 polydimethylsiloxane (for example the one supplied under the trade name of ABIL® EM97 by Evonik Goldschmidt GmbH); and
The third type: an ester emulsifier formed by a polyetherpolyol or a polyol of a non-linear structure or a linear structure, via its hydroxyl group, with a C1-C22 fatty acid, or an ether emulsifier formed by a polyetherpolyol or a polyol, via its hydroxyl group, with a C C22 fatty alcohol, which comprises a polyoxyethylene fatty acid ester, a polyoxyethylene alkyl ether, a mono- or poly- glycerol fatty acid ester, a mono- or poly- glycerol alkyl ether, preferably diisostearyl polyglyceryl- 3 dimer dilinoleate (for example the one supplied under the trade name of ISOLAN® GPS by Evonik Goldschmidt GmbH), polyglyceryl-4 diisostearate/polyhydroxystearate/sebacate (for example the one supplied under the trade name ISOLAN® GPS by Evonik Degussa GmbH),
polyglyceryl-4 stearate (for example the one under the trade name ISOLAN® GI 34) and a polyoxyethylene sorbitan fatty acid ester.
The above cetyl PEG/PPG- 10/1 polydimethylsiloxane (for example the one supplied under the trade name of ABIL EM90 by Evonik
Goldschmidt GmbH) can have the following structure:
wherein R is a cetyl group, x=10, y=l, n= 1-200, o=l-100, m=l-40, the molecular weight of which is 14000g/mol.
Preferably, R1 is an alkyl in the structure of the amido amine of Component b).
Preferably, R1 is a straight or branched alkyl having 15-21 carbon atoms.
Preferably, R is an alkylene in the structure of the amido amine of Component b).
Preferably, R3 and R4 are independently an alkyl in the structure of the amido amine of Component b).
More preferably, the amido amine is
stearamidopropyldimethylamine,
stearamidopropyldiethylamine,
stearamidoethyldiethylamine,
stearamidoethyldimethylamine,
palmitamidopropyldimethylamine,
palmitamidopropyldiethylamine,
palmitamidoethyldiethylamine,
palmitamidoethyldimethylamine,
behenamidopropyldimethylamine,
behenamidopropyldiethylamine,
behenamidoethyldiethylamine,
behenamidoethyldimethylamine,
arachidamidopropyldimethylamine,
arachidamidopropyldiethylamine,
arachidamidoethyldiethylamine,
arachidamidoethyldimethylamine, and
diethylaminoethylstearamide. The fatty acid of Component b) is not limited to straight or branched, saturated or unsaturated fatty acids.
More preferably, the fatty acid of Component b) is selected from lauric acid, isostearic acid, stearic acid, myristic acid, oleic acid and palmitic acid.
Preferably, the equivalent ratio of the fatty acid to the amido amine is 0.5-5: 1, more preferably 0.9-1.5: 1, particularly 1 :1. Optionally, the emulsifier of the present invention further comprises: c) at least one metal salt of a fatty acid, the fatty acid salt having 8-22 carbon atoms.
Preferably, Component a) constitutes 30-90%, more preferably 40-80%, Component b) constitutes 0.5-10%, more preferably 1-8%,
Component c) constitutes 5-65%, more preferably 20-50%,
based on the total weight of the emulsifier composition,
when the metal salt of a fatty acid presents. The fatty acid of Component c) is not limited to straight or branched, saturated or unsaturated fatty acids.
More preferably, the fatty acid of Component c) is selected from lauric acid, isostearic acid, stearic acid, myristic acid, oleic acid and palmitic acid.
Preferably, the metal of Component c) is selected from Ba, Mg, Al, Zn, and Ca.
The present invention furthers provides a water-in-oil emulsion comprising:
d) an oil phase;
e) a water phase;
f) an emulsifier composition of the present invention. Preferably, the oil phase constitutes 15-65%, more preferably 20-50%, the water phase constitutes 30-80%, more preferably 50-80%,
the emulsifier composition constitutes 1-10%, more preferably 2-5%, based on the total weight of the emulsion. Preferably, the oil phase is one or more selected from siloxanes, fatty hydrocarbons, alcohols, esters and ethers.
More preferably, the oil phase is one or more selected from polydimethylsiloxanes, cyclomethicones, aryl- or alkyl- or alkoxy- substituted polydimethylsiloxanes or cyclomethicones, methyl laurate, n- hexyl laurate, 2-ethylhexyl laurate, methyl stearate, isopropyl stearate, n- butyl stearate, octyl stearate, isooctyl stearate, 2-hexyldecyl stearate, steryl heptanoate, methyl oleate, isopropyl oleate, decyl oleate, oleyl oleate, erucyl oleate, decyl linoleate, stearyl heptanoate, isopropyl myristate, myristyl myristate, isopropyl palmitate, octyl palmitate, isononyl palmitate, cetyl palmitate, 2-ethylhexyl palmitate, octyldodecyl 2-palmitate, isononyl isononanoate, cetearyl isononanoate, methyl erueate, oleyl erueate, cetyl ethylhexanoate, cetearyl ethylhexanoate, cetyl ricinoleate, and diisooctyl carbonate, di-n-butyl adipate, di-n-butyl sebacate, di(2-ethylhexyl) adipate, di(2-hexyldecyl) succinate or di-iso- tridecyl azalaate, diethylhexyl carbonate, ethylene glycol dioleate, ethylene glycol diisotridecanoate, propylene glycol di(2-ethylhexanoate), butylene glycol diisostearate, neopentyl glycol dioctoate, decyl cocoate, isocetyl palmitate, triglycerides of the mixture of octanoic acid/decanoic acid, triglycerides of industrial oleic acid, triglycerides of isostearate, triglycerides of the mixture of palmitic acid/oleic acid, caprylic/capric triglyceride, 12-15 alkyl benzoate, isostearyl benzoate, octyldodecyl
benzoate, oleyl alcohol, cetyl alcohol, stearyl alcohol, octyldodecanol, polypropylene glycol- 15 stearyl ether, polypropylene glycol- 14 butyl ether, polypropylene glycol-3 myristyl ether, polypropylene glycol- 11 stearyl ether, dioctyl ether, PPG- 11 stearyl ether, PPG- 15 stearyl ether, PPG- 14 butyl ether, PPG- 3 miristyl ether, paraffin oil, white mineral oil, isohexadecane, polyisobutene, polydecene, petroleum jelly, light liquid paraffin, squalane, olive oil, sunflower seed oil, soybean oil, peanut oil, rapeseed oil, almond oil, palm oil, jojoba oil, coconut oil, liquid fraction of palm shell oil, spermaceti oil, neatsfoot oil, and liquid fraction of tallow oil.
Preferably, the water-in-oil emulsion comprises an optional water miscible alcohol, preferably the water miscible alcohol is one or more selected from monohydric alcohols, diols or triols, more preferably the water miscible alcohol is one or more selected from 1 ,2-proplyene glycol, 1,3-propylene glycol and glycerin.
Preferably, the water-in-oil emulsion further comprises at least one water soluble electrolyte, preferably the electrolyte is one or more selected from sodium chloride, potassium chloride, sodium citrate, sodium lactate, magnesium sulfate, calcium chloride and salts of amino acids.
Optionally, the water-in-oil emulsion further comprises at least one water soluble functional additive for cosmetics, for example, those supplied by Evonik Industries under the trade names TEGO® COSMO C 100, LACTIL® and TEGO® NATURAL BETAIN.
The present invention further provides a process for the preparation of the water-in-oil emulsion of the present invention, comprising:
1) dissolving the emulsifier composition in the oil phase;
2) mixing the water phase and the product obtained in Step 1);
3) homogenizing the mixture obtained in Step 2).
Preferably, Step 1) is carried out at 70-120°C, more preferably at 80- 110°C.
Preferably, Step 2) is carried out at 70-100°C, more preferably at 80- 90°C.
Preferably, Step 3) is carried out at 70-100°C, more preferably at 80- 90°C.
Preferably, Step 3) is carried out at a stirring speed of 1000-10000 rpm, more preferably at a stirring speed of 1500-7500 rpm.
In the water-in-oil emulsion of the present invention, other components generally used in cosmetics, pharmaceuticals, and so on can be arbitrarily incorporated, as necessary, within the range that the effect of the present invention is not undermined.
Examples thereof include UV protection agents, moisturizers, water- soluble polymers, thickeners, coating agents, metal ion sequestering agents, lower alcohols, polyhydric alcohols, pH adjusters, antioxidants, antioxidant aids, and perfumes.
The use application of the water-in-oil emulsion of the present invention is not limited in particular, and the water-in-oil emulsion can be applied in cosmetic products such as pre-makeup, foundation, cheek color, eye shadow, eye liner, sunscreen products, and body-care cosmetics.
Embodiments
Chemicals
Chemicals described below with tradenames have the compositions and commercial availability indicated in Table 1.
Table 1
Formulations
The formulations of the following examples (EX 1-21) and comparative examples (CE 1, 6-10) are listed in Tables 2-20.
Table 2
Table 11
Table 13
Table 15
Table 17
The components of Group A (mainly the oil phase and emulsifier composition) were mixed at 105°C until all the solid ingredients were dissolved completely. Then the mixture of Group A was cooled down to 80°C.
The components of Group B (mainly the water phase) were mixed at 80°C until all the solid ingredients were dissolved completely. Then both
the mixtures of Groups A and B were mixed immediately at 80°C and homogenized for 2-5 minutes at a stirring speed of 1000-10000 rpm.
Optionally, the components of Group C (preservatives) were added soon afterwards.
And the obtained mixture was cooled down to room temperature under stirring.
For Examples 1-21, stable and homogenized water- in-oil emulsion systems were obtained. However, for Comparative Examples 1, 6-10, such systems were not obtained, and layer separation was observed within one minute after the homogenization stopped.
Claims
1. An emulsifier composition, comprising
a) at least one water-in-oil emulsifier;
b) at least one fatty acid salt of an amido amine or the precursor mixture thereof consisting of the corresponding fatty acid and the amido amine, the fatty acid having 8-22 carbon atoms,
the amido amine having the following structure,
R1-C(0)-NH-R2-N(R3)(R4); wherein
R1 is an aliphatic hydrocarbyl group having 7-21 carbon atoms;
R2 is a hydrocarbylene group having 1-4 carbon atoms;
R3 and R4 are independently a hydrocarbyl group having 1-4 carbon atoms;
2. The emulsifier composition according to Claim 1, wherein
Component a) constitutes 50-99.5%, preferably 80-99%,
Component b) constitutes 0.5-50%, preferably 1-20%,
based on the total weight of the emulsifier composition.
3. The emulsifier composition according to Claim 1, further comprising: c) at least one metal salt of a fatty acid, the fatty acid salt having 8-22 carbon atoms.
4. The emulsifier composition according to Claim 3, wherein
Component a) constitutes 30-90%, preferably 40-80%,
Component b) constitutes 0.5-10%, preferably 1-8%,
Component c) constitutes 5-65%, preferably 20-50%,
based on the total weight of the emulsifier composition.
5. The emulsifier composition according to any one of preceding claims, wherein Component a) is selected from
surfactants having an HLB value less than 12, preferably an HLB value from 2-8,
the surfactants having hydrophilic groups selected from polyoxyethylene groups, polyoxypropylene groups, polyglycerol groups, polyoxyethylene sorbitan groups.
6. The emulsifier composition according to any one of preceding claims, wherein Component a) is one or more selected from the following three types:
the first type: an emulsifier having a molecular chain structure of polysiloxane + a hydrophilic group + an alkyl, which comprises a block copolymer emulsifier of polysiloxane, a polyetherpolyol and a C1-C22 aliphatic alkane connected by covalent bonds, an emulsifier with a polysiloxane chain as the main chain, and polyetherpolyol and Q-C22 aliphatic alkyl as side groups which are respectively connected to the main chain of polysiloxane by covalent bonds, and an emulsifier with a polysiloxane chain as the main chain, C1-C22 aliphatic alkyl modified polyetherpolyol as side groups which are connected to the polysiloxane chain by covalent bonds; the second type: an emulsifier having a molecular chain structure of polysiloxane + a hydrophilic group, which emulsifier comprises a block copolymer emulsifier with polysiloxane and a polyetherpolyol connected by covalent bonds, an emulsifier with a polysiloxane chain as the main chain, and polyetherpolyol as side groups connected to the main chain of polysiloxane by covalent bonds; and the third type: an ester emulsifier formed by a polyetherpolyol or polyol of a non-linear structure or a linear structure, via its hydroxyl group, with a C1-C22 fatty acid, or an ether emulsifier formed by a polyetherpolyol or polyol, via its hydroxyl group, with a C1-C22 fatty alcohol, which comprise a polyoxyethylene fatty acid ester, a polyoxyethylene alkyl ether, a mono- or poly- glycerol fatty acid ester, a mono- or polyglycerol alkyl ether.
7. The emulsifier composition according to any one of preceding claims, wherein Component a) is selected from
polyoxyethylene polydimethylsiloxane,
polyglycerol polydimethylsiloxane,
bis-PEG/PPG- 14/14 polydimethylsiloxane,
diisostearyl polyglyceryl-3dimer dilinoleate,
polyglyceryl-4 diisostearate/polyhydroxystearate/sebacate,
polyglyceryl-4 stearate,
polyoxyethylene sorbitan fatty acid ester, and
the cetyl PEG/PPG- 10/1 polydimethylsiloxane having the following structure:
wherein R is a cetyl group, x=10, y=l, n= 1-200, o=l-100, m=l-40, the molecular weight of which is 14000g/mol,
preferably Component a) is the product under the trade name ABIL® EM90 or ABIL® EM 180 provided by Evonik Goldschmidt GmbH.
8. The emulsifier composition according to any one of preceding claims, wherein
R1 is an alkyl, preferably an alkyl having 15-21 carbon atoms,
R2 is an alkylene,
R3 and R4 are independently an alkyl,
and more preferably, the amido amine of Component b) is selected from stearamidopropyldimethylamine,
stearamidopropyldiethylamine,
stearamidoethyldiethylamine,
stearamidoethyldimethylamine,
palmitamidopropyldimethylamine,
palmitamidopropyldiethylamine,
palmitamidoethyldiethylamine,
palmitamidoethyldimethylamine,
behenamidopropyldimethylamine,
behenamidopropyldiethylamine,
behenamidoethyldiethylamine,
behenamidoethyldimethylamine,
arachidamidopropyldimethylamine,
arachidamidopropyldiethylamine,
arachidamidoethyldiethylamine,
arachidamidoethyldimethylamine, and
diethylaminoethylstearamide.
9. The emulsifier composition according to any one of preceding claims, wherein the fatty acid of Component b) is selected from
lauric acid, isostearic acid, stearic acid, myristic acid, oleic acid and palmitic acid.
10. The emulsifier composition according to any one of preceding claims, wherein in the precursor mixture, the equivalent ratio of the fatty acid to the amido amine is 0.5-5: 1, preferably 0.9-1.5: 1, more preferably 1 :1.
11. The emulsifier composition according to any one of Claims 3-10, wherein the fatty acid of Component c) is selected from
lauric acid, isostearic acid, stearic acid, myristic acid, oleic acid and palmitic acid.
12. The emulsifier composition according to any one of preceding claims, wherein the metal of Component c) is selected from Ba, Mg, Al, Zn, and Ca.
13. A water-in-oil emulsion, comprising
d) an oil phase;
e) a water phase;
f) an emulsifier composition according to any one of preceding claims.
14. The water-in-oil emulsion according to Claim 13, wherein
the oil phase constitutes 15-65%, preferably 20-50%,
the water phase constitutes 30-80%, preferably 50-80%,
the emulsifier composition constitutes 1-10%, preferably 2-5%,
based on the total weight of the emulsion.
15. The water-in- oil emulsion according to Claim 13 or 14, wherein the oil phase is one or more selected from siloxanes, fatty hydrocarbons, alcohols, esters and ethers.
16. The water-in- oil emulsion according to any one of Claims 13-15, wherein the oil phase is one or more selected from
polydimethylsiloxanes, cyclomethicones, aryl- or alkyl- or alkoxy- substituted polydimethylsiloxanes or cyclomethicones, methyl laurate, n- hexyl laurate, 2-ethylhexyl laurate, methyl stearate, isopropyl stearate, n- butyl stearate, octyl stearate, isooctyl stearate, 2-hexyldecyl stearate, steryl heptanoate, methyl oleate, isopropyl oleate, decyl oleate, oleyl oleate, erucyl oleate, decyl linoleate, stearyl heptanoate, isopropyl myristate, myristyl myristate, isopropyl palmitate, octyl palmitate, isononyl palmitate, cetyl palmitate, 2-ethylhexyl palmitate, octyldodecyl 2-palmitate, isononyl isononanoate, cetearyl isononanoate, methyl erueate, oleyl erueate, cetyl ethylhexanoate, cetearyl ethylhexanoate, cetyl ricinoleate, and diisooctyl carbonate, di-n-butyl adipate, di-n-butyl sebacate, di(2-ethylhexyl) adipate, di(2-hexyldecyl) succinate or di-iso- tridecyl azalaate, diethylhexyl carbonate, ethylene glycol dioleate, ethylene glycol diisotridecanoate, propylene glycol di(2-ethylhexanoate), butylene glycol diisostearate, neopentyl glycol dioctoate, decyl cocoate, isocetyl palmitate, triglycerides of the mixture of octanoic acid/decanoic acid, triglycerides of industrial oleic acid, triglycerides of i so stearate, triglycerides of the mixture of palmitic acid/oleic acid, caprylic/capric triglyceride, 12-15 alkyl benzoate, isostearyl benzoate, octyldodecyl benzoate, oleyl alcohol, cetyl alcohol, stearyl alcohol, octyldodecanol, polypropylene glycol- 15 stearyl ether, polypropylene glycol- 14 butyl ether, polypropylene glycol-3 myristyl ether, polypropylene glycol- 11 stearyl ether, dioctyl ether, PPG- 11 stearyl ether, PPG- 15 stearyl ether, PPG- 14 butyl ether, PPG- 3 miristyl ether, paraffin oil, white mineral oil, isohexadecane, polyisobutene, polydecene, petroleum jelly, light liquid paraffin, squalane, olive oil, sunflower seed oil, soybean oil, peanut oil, rapeseed oil, almond oil, palm oil, jojoba oil, coconut oil, liquid fraction of palm shell oil, spermaceti oil, neatsfoot oil, and liquid fraction of tallow oil.
17. The water-in-oil emulsion according to any one of Claims 13-16, wherein the water-in-oil emulsion comprises an optional water miscible alcohol,
preferably the water miscible alcohol is one or more selected from monohydric alcohols, diols or triols,
more preferably the water miscible alcohol is one or more selected from 1,2-proplyene glycol, 1,3-propylene glycol and glycerin.
18. The water-in-oil emulsion according to any one of Claims 13-17, wherein the water-in-oil emulsion further comprises a water soluble electrolyte,
preferably the electrolyte is one or more selected from sodium chloride, potassium chloride, sodium citrate, sodium lactate, magnesium sulfate, calcium chloride and salts of amino acids.
19. A process for the preparation of the water-in-oil emulsion, according to any one of Claims 13-18, comprising
1) dissolving the emulsifier composition in the oil phase;
2) mixing the water phase and the product obtained in Step 1);
3) homogenizing the mixture obtained in Step 2).
20. The process according to Claim 19, wherein
Step 1) is carried out at 70-120°C, preferably 80-110°C,
Step 2) is carried out at 70-100°C, preferably 80-90°C,
Step 3) is carried out at 70-100°C, preferably 80-90°C.
21. The process according to Claim 19 or 20, wherein
Step 3) is carried out at a stirring speed of 1000-10000 rpm, preferably 1500-7500 rpm.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/CN2012/075451 WO2013170419A1 (en) | 2012-05-14 | 2012-05-14 | Emulsifier composition and the use thereof |
| CN201280073199.XA CN104284970B (en) | 2012-05-14 | 2012-05-14 | Emulsifier combination and application thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/CN2012/075451 WO2013170419A1 (en) | 2012-05-14 | 2012-05-14 | Emulsifier composition and the use thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2013170419A1 true WO2013170419A1 (en) | 2013-11-21 |
Family
ID=49582967
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/CN2012/075451 Ceased WO2013170419A1 (en) | 2012-05-14 | 2012-05-14 | Emulsifier composition and the use thereof |
Country Status (2)
| Country | Link |
|---|---|
| CN (1) | CN104284970B (en) |
| WO (1) | WO2013170419A1 (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104705480A (en) * | 2015-03-24 | 2015-06-17 | 湖州珍贝羊绒制品有限公司 | Compound degreasing agent for animal fur fiber and degreasing method of compounding degreasing agent |
| CN104906553A (en) * | 2015-07-09 | 2015-09-16 | 上海贝泰妮生物科技有限公司 | Water-in-oil baby nappy cream and preparation method thereof |
| CN108208194A (en) * | 2016-12-09 | 2018-06-29 | 嘉里特种油脂(上海)有限公司 | A kind of impervious fluid composition |
| US10045922B1 (en) | 2017-05-30 | 2018-08-14 | Kokyu Alcohol Kogyo Co., Ltd. | W/O type emulsion and a premix for producing the same |
| WO2019095364A1 (en) * | 2017-11-20 | 2019-05-23 | Evonik Degussa Gmbh | Water in oil emulsifier composition and the use thereof |
| CN119979255A (en) * | 2025-02-08 | 2025-05-13 | 山东三晶润滑科技有限公司 | A kind of degradable natural plant extraction emulsified oil for hydraulic support and preparation method thereof |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105854965B (en) * | 2016-06-12 | 2019-04-12 | 北京天天极因科技有限公司 | A kind of oil phase composition generating Water-In-Oil drop for centrifugal process |
| CN106967991A (en) * | 2017-02-24 | 2017-07-21 | 谢松甫 | Iron wire degreasing, the method for impurity elimination and its application in zinc-plated production technology |
| CN117241878A (en) | 2021-03-05 | 2023-12-15 | 伊努梅里斯公司 | Systems and methods for generating droplets and performing digital analysis |
| EP4351788A4 (en) | 2021-06-04 | 2025-04-09 | Enumerix, Inc. | COMPOSITIONS, METHODS AND SYSTEMS FOR SINGLE CELL BARCODING AND SEQUENCED CELLS |
| US12252745B2 (en) | 2021-09-02 | 2025-03-18 | Enumerix, Inc. | Detection and digital quantitation of multiple targets |
| EP4453246A1 (en) | 2021-12-20 | 2024-10-30 | Enumerix, Inc. | Detection and digital quantitation of multiple targets |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070093409A1 (en) * | 2005-10-24 | 2007-04-26 | Panandiker Rajan K | Fabric care compositions and systems comprising organosilicone microemulsions and methods employing same |
| CN101862620A (en) * | 2009-04-16 | 2010-10-20 | 赢创高施米特有限公司 | Emulsifier comprising glycerol-modified organopolysiloxane |
| CN101987069A (en) * | 2009-07-31 | 2011-03-23 | 赢创德固赛(中国)投资有限公司 | Thermally stable oil-in-water microemulsion |
-
2012
- 2012-05-14 WO PCT/CN2012/075451 patent/WO2013170419A1/en not_active Ceased
- 2012-05-14 CN CN201280073199.XA patent/CN104284970B/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070093409A1 (en) * | 2005-10-24 | 2007-04-26 | Panandiker Rajan K | Fabric care compositions and systems comprising organosilicone microemulsions and methods employing same |
| CN101862620A (en) * | 2009-04-16 | 2010-10-20 | 赢创高施米特有限公司 | Emulsifier comprising glycerol-modified organopolysiloxane |
| CN101987069A (en) * | 2009-07-31 | 2011-03-23 | 赢创德固赛(中国)投资有限公司 | Thermally stable oil-in-water microemulsion |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104705480A (en) * | 2015-03-24 | 2015-06-17 | 湖州珍贝羊绒制品有限公司 | Compound degreasing agent for animal fur fiber and degreasing method of compounding degreasing agent |
| CN104906553A (en) * | 2015-07-09 | 2015-09-16 | 上海贝泰妮生物科技有限公司 | Water-in-oil baby nappy cream and preparation method thereof |
| CN104906553B (en) * | 2015-07-09 | 2018-10-16 | 昆明贝泰妮生物科技有限公司 | A kind of Water-In-Oil infant buttocks-care cream and preparation method thereof |
| CN108208194A (en) * | 2016-12-09 | 2018-06-29 | 嘉里特种油脂(上海)有限公司 | A kind of impervious fluid composition |
| CN108208194B (en) * | 2016-12-09 | 2021-12-31 | 嘉里特种油脂(上海)有限公司 | Impervious oil composition |
| US10045922B1 (en) | 2017-05-30 | 2018-08-14 | Kokyu Alcohol Kogyo Co., Ltd. | W/O type emulsion and a premix for producing the same |
| EP3409262A1 (en) * | 2017-05-30 | 2018-12-05 | Kokyu Alcohol Kogyo Co., Ltd. | W/o type emulsion and a premix for producing the same |
| CN108969387A (en) * | 2017-05-30 | 2018-12-11 | 高级醇工业株式会社 | W/o type emulsion and premix for manufacturing the emulsion |
| US10328006B2 (en) | 2017-05-30 | 2019-06-25 | Kokyu Alcohol Kogyo Co., Ltd. | W/O type emulsion and a premix for producing the same |
| WO2019095364A1 (en) * | 2017-11-20 | 2019-05-23 | Evonik Degussa Gmbh | Water in oil emulsifier composition and the use thereof |
| CN119979255A (en) * | 2025-02-08 | 2025-05-13 | 山东三晶润滑科技有限公司 | A kind of degradable natural plant extraction emulsified oil for hydraulic support and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN104284970B (en) | 2018-03-09 |
| CN104284970A (en) | 2015-01-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO2013170419A1 (en) | Emulsifier composition and the use thereof | |
| KR101087602B1 (en) | External skin composition | |
| AU2010334096B2 (en) | Sheet-like cosmetic | |
| JP5731138B2 (en) | Water-in-oil emulsifier composition, water-in-oil emulsified composition using the composition, and cosmetics | |
| JP2003231627A (en) | Skin care composition | |
| JP2010530456A (en) | Stable high internal phase emulsion and composition thereof | |
| KR101453808B1 (en) | Water-in-oil-type skin-whitening cosmetic | |
| TW201907898A (en) | W/O type emulsion | |
| JP2002193740A (en) | O / W emulsion composition | |
| JP7587916B2 (en) | Emulsion composition for external use | |
| CN114146010B (en) | Anhydrous sun-screening gel containing oil-soluble sun-screening agent and preparation method thereof | |
| KR20140012695A (en) | Manufacturing method for o/w emulsion composition | |
| CN102379828B (en) | Comprise the compositions of the containing amino-functional silicone gum of organic silicone oil bag water emulsifier and low nitrogen content | |
| CN110167519A (en) | It is suitble to clean composition | |
| WO2020075795A1 (en) | Oil-in-water emulsion cosmetic | |
| JP2010222317A (en) | Oil-in-water type emulsified cosmetic | |
| CZ315096A3 (en) | Cosmetic compositions based on oil-in-water emulsion intended for skin care | |
| EP3713538A1 (en) | Water in oil emulsifier composition and the use thereof | |
| WO2024033154A1 (en) | Emulsion deodorant compositions | |
| JP2024057429A (en) | Water-in-oil emulsion cosmetics | |
| WO2012137500A1 (en) | Composition for melanin pigment excretion | |
| JP7773003B1 (en) | W/O/W emulsion and its manufacturing method | |
| JP2009149623A (en) | Emulsion cosmetic for skin | |
| WO2025234146A1 (en) | W/o/w-type emulsion and method for producing same | |
| WO2025234144A1 (en) | W/o/w-type emulsion and production method therefor |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 12876694 Country of ref document: EP Kind code of ref document: A1 |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 12876694 Country of ref document: EP Kind code of ref document: A1 |