WO2020052913A1 - Préparation nettoyante moussante à base d'une émulsion - Google Patents

Préparation nettoyante moussante à base d'une émulsion Download PDF

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Publication number
WO2020052913A1
WO2020052913A1 PCT/EP2019/072081 EP2019072081W WO2020052913A1 WO 2020052913 A1 WO2020052913 A1 WO 2020052913A1 EP 2019072081 W EP2019072081 W EP 2019072081W WO 2020052913 A1 WO2020052913 A1 WO 2020052913A1
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Prior art keywords
weight
preparation according
emulsifier
preparation
cleaning preparation
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Ceased
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PCT/EP2019/072081
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German (de)
English (en)
Inventor
Julia NEMNICH
Marcel Lex
Katharina Reiter
Benedict Resch
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Beiersdorf AG
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Beiersdorf AG
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Priority to EP19756347.1A priority Critical patent/EP3849502A1/fr
Publication of WO2020052913A1 publication Critical patent/WO2020052913A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • 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
    • A61Q19/10—Washing or bathing preparations
    • 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
    • A61K8/342—Alcohols having more than seven atoms in an unbroken chain
    • 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
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37—Esters of carboxylic acids
    • A61K8/375—Esters of carboxylic acids the alcohol moiety 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
    • A61K8/40—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
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/463—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
    • 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
    • A61K8/73—Polysaccharides
    • A61K8/737—Galactomannans, e.g. guar; Derivatives 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
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8158—Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; Compositions of derivatives of such polymers
    • 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
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/02—Preparations for cleaning the hair
    • 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
    • A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/26—Optical properties

Definitions

  • the present invention relates to a foaming, cosmetic cleaning preparation with an opaque appearance, which is achieved in that the preparation is in the form of an emulsion.
  • Cleaning products are designed to clean the skin and hair. After the cleaning process, the user ideally has a feeling of cleanliness, freshness and well-being. Humans have always had the need to cleanse themselves, i.e. Remove dirt from the skin or hair. Over time, the cleaning processes have changed, as have the products that are used for cleaning.
  • the skin is cleaned, for example, by washing, shower baths or bath tubs, while the hair is often also cleaned during the shower bath or bath tub or also washed separately.
  • Body cleansing products primarily serve to remove dirt from the skin surface.
  • the dirt film consists of solid or liquid components that have reached the skin from the outside. Excess skin lipids and dead body cells also belong to the dirt film. The components of the dirt film get into the wash liquor through surface-active ingredients in the cleaning compositions and are removed from the skin by the rinsing process.
  • the products should be easy to distribute in the hair, the foam should form quickly, the hair should be cleaned and cared for gently and gently. In addition, it should be easy to wash out and wet hair should have a pleasant feel and be easy to comb. Dry hair should also be easy to comb, the appearance of the hair should be natural and it should shine. The products are said to make the hair supple and not to weigh it down. In addition, rapid relubrication should be prevented. So there is a long catalog of requirements in the area of hair cleaning, which at least to a large extent has to be fulfilled in order to be able to sell a product that is accepted by the consumer.
  • a cleaning preparation also plays an important role in the acceptance of a product by the consumer. Cleaning preparations in a white color are very attractive for the customer. The white color associates purity and cleanliness. If a white cleaning preparation also has a creamy consistency, the customer also associates good care with this product.
  • Opaque or "white” cleaning compositions are known per se. To give cleaning compositions this appearance, opacifiers or pearlescent agents are generally used. Pearlescent agents can be heavy metal salts of higher fatty acids, fatty acid esters or fatty acid diesters of polyols or fatty acid alkanolamide derivatives. These substances exist as crystal platelets or rods and reflect the light. Opacifiers have no pearlescent effect per se.
  • a known and frequently used group of opacifiers are sodium salts of a polymer of styrene monomers with monomers of acrylic acid, methacrylic acid and / or another olefin and / or one of their esters, e.g. Polymers with the INCI name Styrene / Acrylates Copolymer. Styrenes / acrylates copolymer is present in the cosmetic preparations in the form of particles with particle sizes of approximately 170 nm.
  • This particle size is in the range of the particle size defined by some environmental organizations for the particle size of microplastics.
  • Microplastics can be understood to mean plastic particles that are 5 mm and smaller. These particles can be detected in rivers and seas and are considered harmful to the environment.
  • foam especially a creamy, soft foam
  • foam is very important for cleaning preparations for cleaning the hair and the body.
  • the consumer With a sufficient amount of foam, the consumer generally combines good cleaning performance.
  • a good care performance is often associated with a creamy, soft foam.
  • the solution to this problem can be to add foam-forming surfactants to the preparations mentioned.
  • Conditioning shampoos are disclosed in document WO 2007/104740 A1. These shampoos can be in the form of an emulsion which contains an oil phase and a water phase, the emulsion
  • One or more surfactants are provided.
  • At least one surfactant preferably at least one anionic surfactant selected from alkyl ether sulfates and optionally at least one amphoteric surfactant and
  • At least one conditioning agent in particular at least one cationic polymer and / or ampholytic polymer,
  • the preparation according to the invention is a cosmetic preparation.
  • the preparation according to the invention is an aqueous preparation
  • the water content is advantageously 50 to 80% by weight, preferably 60 to 70% by weight, based on the total weight of the preparation.
  • the preparation according to the invention is used to clean the hair and skin.
  • the product forms include body cleansing products such as shower baths, bubble baths, liquid soaps, foaming facial cleansers, and others.
  • Body cleansing products such as shower baths, bubble baths, liquid soaps, foaming facial cleansers, and others.
  • Product forms for hair cleaning for example hair shampoos, conditioning shampoos and others, are also included.
  • the present invention also relates to the use of a cosmetic cleaning preparation comprising
  • the at least one O / W emulsifier being in the form of an emulsifier mixture, comprising at least one glyceryl partial ester with fatty acids saturated with C14-C22 and at least one alkali salt of a C14-C22 fatty acid, in particular comprising an emulsifier mixture Glyceryl stearate and sodium and / or potassium stearate,
  • At least one fatty alcohol at least one surfactant, preferably at least one anionic surfactant, selected from alkyl ether sulfates and optionally at least one amphoteric surfactant and
  • At least one conditioning agent in particular at least one cationic polymer, for the nourishing cleaning of the skin and hair.
  • the present invention also relates to a process for producing a foaming, opaque cleaning preparation, no opacifiers and no pearlescent agents being added to the preparation, and the preparation being in the form of an emulsion.
  • the present invention likewise relates to a method for producing an opaque, stable cleaning preparation in that the preparation comprises at least one O / W emulsifier consisting of a mixture of at least one glyceryl partial ester with fatty acids saturated with C14-C22 and at least one alkali metal salt C14-C22 fatty acid, in particular an emulsifier mixture comprising glyceryl stearate and sodium and / or potassium stearate, is added.
  • O / W emulsifier consisting of a mixture of at least one glyceryl partial ester with fatty acids saturated with C14-C22 and at least one alkali metal salt C14-C22 fatty acid, in particular an emulsifier mixture comprising glyceryl stearate and sodium and / or potassium stearate, is added.
  • Emulsifiers ensure that two immiscible liquids (e.g. oil in water) can form a stable emulsion.
  • Emulsifiers have an amphiphilic character, some of the molecule is lipophilic, the other hydrophilic.
  • the lipophilic part of the emulsifier is soluble in oil and protrudes into the oil.
  • An oil droplet is formed by stirring and is dispersed in the aqueous environment by the hydrophilic part of the emulsifier.
  • emulsifiers have no wash-active, surfactant character.
  • Emulsifiers reduce the interfacial tension between the two phases and, in addition to reducing the interfacial work, they also stabilize the emulsion formed. They stabilize the emulsion formed by interfacial films and by the formation of steric or electrical barriers, which prevents the coalescence of the emulsified particles.
  • emulsifiers In order for compounds to be effective as emulsifiers, they must have a certain molecular structure.
  • the structural characteristic of such compounds is their amphiphilic molecular structure.
  • the molecule of such a compound has at least one group with affinity for substances of strong polarity (polar group) and at least one group with affinity for non-polar substances (apolar group).
  • polar group substances of strong polarity
  • apolar group a distinction is made between nonionic, anionic and cationic emulsifiers.
  • emulsifiers with an HLB value of up to approx. 8 are considered W / O emulsifiers.
  • O / W emulsifiers have HLB values of greater than 8 to 15.
  • Substances with HLB values greater than 15 are often referred to as solubilizers.
  • the preparation according to the invention contains O / W emulsifiers in the form of an emulsifier mixture comprising at least one glyceryl partial ester with C14-C22 saturated fatty acids and at least one alkali salt of a C14-C22 fatty acid, in particular an emulsifier mixture comprising glyceryl stearate and sodium and / or potassium Stearate.
  • the emulsifier mixture contains at least 30% monoglyceride esters, advantageously between 32 and 50%.
  • the content of the alkali salt in the emulsifier mixture is advantageously between 2 and 10% by weight, particularly advantageously between 4 and 6% by weight, based on the emulsifier mixture.
  • Such mixtures are available, for example, with the INCI name Glyceryl Steakate SE and can be obtained as Tegin® from Evonik, as Cutina® GMS SE from BASF and as Imwitor® 960K from Sasol.
  • An HLB value of 12 is given for the emulsifier Gly ceryl Stearate SE.
  • the content of O / W emulsifiers in the form of an emulsifier mixture and comprising at least one glyceryl partial ester saturated with C14-C22 fatty acids and at least one alkali salt of a C14-C22 fatty acid is preferably at least 1.5% by weight from 2 to 8% by weight, particularly preferably from 3 to 7% by weight, based on the total weight of the preparation. This information relates to the raw material content.
  • the preparation according to the invention can additionally contain at least one W / O emulsifier.
  • This additional W / O emulsifier is preferably selected from partial esters of polyols with 3 to 6 carbon atoms with saturated C8-C22 carboxylic acids, particularly preferably from glycerol partial esters with saturated C14-C20 fatty acids, particularly preferred is glyceryl stearate, that for example, under the trade name Tegin M from Evonik who can.
  • This emulsifier has an HLB value of about 4 and can therefore be classified as a W / O emulsifier.
  • the preparation according to the invention contains at least one additional W / O emulsifier, this is at least one additional W / O emulsifier in the preparation according to the invention with a total content of 2 to 6% by weight, preferably 3 to 5% by weight. based on the active content and the total weight of the preparation included.
  • emulsifiers in particular O / W emulsifiers, which are distinguished by the fact that they contain ethylene oxide residues and / or propylene oxide residues. Ethoxylated and / or propoxylated fatty acids and / or fatty alcohols are often used.
  • the preparation according to the invention contains no polyethoxylated and / or polypropoxylated emulsifiers, in particular no polyethoxylated and / or polypropoxylated O / W emulsifiers.
  • the preparation according to the invention is therefore free from ethoxylated and / or propoxylated emulsifiers;
  • the preparation according to the invention is therefore in particular free of ethoxylated and / or propoxylated O / W emulsifiers.
  • Free from in the sense of the present invention means that 0 to 0.1% by weight, preferably 0 to 0.01% by weight, particularly preferably 0% by weight, based on the total weight of the preparation, of the particular Substance present in the preparation.
  • the preparation according to the invention contains at least one fatty alcohol.
  • Fatty alcohols are e.g. straight or branched chain aliphatic monohydric alcohols with 6 - 22 carbon atoms.
  • Straight-chain fatty alcohols with a chain length of 12 - 18 carbon atoms are preferably used in cosmetics. These fatty alcohols are soft, colorless masses, practically non-toxic and well tolerated by the skin.
  • Cetyl alcohol, stearyl alcohol and cetearyl alcohol are of particular importance in cosmetics.
  • the preparation according to the invention advantageously contains at least one fatty alcohol which is selected from the group consisting of cetyl alcohol, stearyl alcohol and cetearyl alcohol.
  • the at least one fatty alcohol is advantageously present in the preparation according to the invention with a content of 1.0 to 10.0% by weight, preferably 3.0 to 7.0% by weight, based on the total weight of the preparation.
  • the preparation according to the invention contains at least one surfactant.
  • Surfactants can be divided into anionic, cationic, amphoteric and nonionic surfactants.
  • the surfactants which are used in the preparation according to the invention are partially anionic surfactants, optionally in combination with amphoteric surfactants.
  • Anionic surfactants generally have carboxylate, sulfate or sulfonate groups as functional groups. In aqueous solution they form negatively charged organic ions in an alkaline or neutral environment.
  • Suitable anionic surfactants are
  • acylglutamates for example sodium acylglutamate, sodium cocoylglutamate, di-TEA-palmitoylaspartate and sodium caprylic / capric glutamate,
  • acyl peptides for example palmitoyl-hydrolyzed milk protein, sodium cocoyl-hydrolyzed soy protein and sodium / potassium-cocoyl-hydrolyzed collagen,
  • sarcosinates for example myristoyl sarcosin, TEA-lauroyl sarcosinate, sodium lauroyl sarcosinate and sodium cocoyl sarcosinate,
  • Carboxylic acids and derivatives such as
  • ester carboxylic acids for example acyl lactylates, such as lauroyl lactylate, caproyl lactylate, calcium stearoyl lactylate, laureth-6-citrate and sodium PEG-4-lauramide carboxylate,
  • ether carboxylic acids for example sodium laureth-13 carboxylate and sodium
  • Phosphoric acid esters and salts such as DEA-oleth-10-phosphate and dilaureth-phosphate,
  • acyl isethionates e.g. Sodium / ammonium cocoyl isethionate, sodium lauryl methyl isethionate,
  • taurates for example sodium lauroyl taurate and sodium methyl cocoyl taurate
  • alkyl sulfonates for example sodium coconut monoglyceride sulfate, sodium C12-14 olefin sulfonate, sodium lauryl sulfoacetate and magnesium PEG-3 cocamide sulfate, 5.
  • Sulfosuccinates for example dioctyl sodium sulfosuccinate, disodium laureth sulfosuccinate, disodium lauryl sulfosuccinate, disodium undecylenamido MEA sulfosuccinate and PEG-5 lauryl citrate sulfosuccinate. such as
  • Sulfuric acid esters such as
  • Alkyl sulfates for example sodium, ammonium and TEA lauryl sulfate, sodium ammonium and TEA coco sulfate.
  • the preparation according to the invention contains at least one alkyl ether sulfate, it is particularly preferred if the alkyl groups of the at least one alkyl ether sulfate according to the invention have 8 to 18, particularly preferably 10 to 14, carbon atoms. It is also particularly preferred if Na + is selected from the group of suitable cations of the alkyl ether sulfates.
  • the incorporation of sodium laureth sulfate into the preparation according to the invention is very particularly particularly preferred, and it is also very particularly preferred if the content of sodium laureth sulfate is greater than 2% by weight, based on the total weight of the preparation.
  • the total content of the at least one anionic surfactant in the preparation according to the invention is 2.0 to 20.0% by weight, preferably 5 to 18% by weight, particularly preferably 7 to 16% by weight, based on the total weight of the preparation and the respective active content.
  • the total amount of the anionic surfactant (s) contains the content of at least one alkyl ether sulfate.
  • the preparation according to the invention contains photic surfactants.
  • Suitable amphoteric surfactants are
  • Acyl- / dialkylethylenediamine for example sodium acylamphoacetate, disodium macylamphodipropionate, disodium alkylamphodiacetate, disodium cocoamphodiacetate, disodium cocoamphomonoacetate, sodium acylamphohydroxypropylsulfonate, disodium triamylamphamiacodiacetate and sodium acacid
  • N-alkylamino acids for example aminopropylalkylglutamide, alkylaminopropionic acid, sodium alkylimidodipropionate and lauroamphocarboxyglycinate.
  • betaines for example coco betaines, cocoamidopropyl betaines,
  • Sultaine for example Lauryl Hydroxy Sultaine.
  • the at least one amphoteric surfactant is preferably selected from the group alkylamido propyl betaines and alkyl betaines. It is particularly preferred if the amphoteric surfactant is cocamidopropyl betaine.
  • the total content of the at least one amphoteric surfactant is 0.5 to 10.0% by weight, preferably 1.0 to 7.0% by weight, particularly preferably 2.0 to 5 , 0 wt .-%, based on the total weight of the preparation and the respective active content.
  • the preparation according to the invention contains at least one conditioning agent.
  • Conditioning agents belong to different chemical classes of compounds. However, the conditioners have in common that they interact with the surface of the skin and / or hair. With regard to hair, conditioners are often described with the term that the conditioners apply to the hair. After the respective preparation has been rinsed out, the conditioning agents should at least partially remain on the hair and thus improve the combability, the feel and the shine of the hair.
  • the conditioning agents can be roughly divided into water-soluble and water-insoluble conditioning agents.
  • Cationic surfactants and polymers can be added to the water-soluble conditioning agents.
  • Oils, fats, waxes and silicones can be added to the water-insoluble conditioning agents.
  • Cationic polymers are polymeric compounds which have cationic groups in the main and / or side chain. These groups can be temporarily cationic. These are, for example, primary, secondary or tertiary amine groups which are present as positively charged groups at suitable pH values.
  • Permanent cationic groups are always positively charged regardless of the pH. It is usually a quaternary nitrogen atom, for example in the form of an ammonium group.
  • Cationic polymers can be natural polymers which have been modified such that, for example, permanent cationic groups, in particular quaternary ammonium groups, have been introduced into the molecule. Quaternary ammonium groups are preferred cationic groups according to the invention. These groups can be introduced into cellulose molecules or guar molecules, for example.
  • Cationic guar derivatives are particularly preferred according to the invention in the preparation according to the invention, in particular guar hydroxypropyltrimonium chloride, which is available, for example, from the company Rhodia under the trade name Jaguar C-14 S.
  • Cationic polymers can also be synthetic polymers containing monomers with cationic groups. It is preferred here if the monomer with the cationic group has a permanently cationic group; dimethyl dialyl ammonium chloride is particularly preferred as the monomer.
  • a particularly preferred cationic synthetic polymer is Polyquaternium-6, which is available, for example, as Merquat 100 from Lubrizol.
  • polyquaternium-7 Another particularly preferred synthetic cationic polymer which contains the monomer dimethyl diallyl ammonium chloride in addition to the monomer acrylamide is polyquaternium-7.
  • This polymer is available, for example, as Mirapol 550 P from Sol vay.
  • Ampholytic polymers can also be selected as conditioning agents to be used advantageously.
  • these polymers also contain monomers with an anionic functionality.
  • An example of such poly mers is Polyquaternium-53, which according to the invention is also particularly preferably used is.
  • Polyquaternium-53 can be obtained, for example, from Lubrizol under the trade name Merquat 2003PR.
  • the particularly preferred cationic polymers guar hydroxytrimonium chloride, polyquternium-6 and polyquaternium-7 and the ampholytic polymer polyquaternium-53 can be used individually in the preparation according to the invention or in combinations of two, three or four. It is furthermore advantageous if only the cationic polymers are selected from the group consisting of guar hydroxytrimonium chloride, polyquternium-6, polyquaternium-7 and / or polyquaternium-53.
  • the total content of the at least one cationic and / or ampholytic polymer in the preparation according to the invention is 0.1 to 5.0% by weight, preferably 0.2 to
  • the preparation according to the invention advantageously contains emollients. These components counteract drying out and help to reduce the loss of moisture in hair. In addition, they often also have a smoothing effect on the surface of the hair.
  • Various classes of compounds can be included in the emollients.
  • ester oils are characterized by the fact that saturated or unsaturated C6-C22 fatty acids are esterified with branched or unbranched C4-C20 alcohols. Examples of such compounds are ethylhexyl palmitate, ethylhexyl stearate, hexyl laurate, dibutyl adipate, decyl oleate, hexyl decyl stearate, isopropyl myristate, isopropyl palmitate, myristyl myristate and cetyl palmitate.
  • the preparation according to the invention preferably contains isopropyl palmitate and / or isopropyl myristate.
  • the total content of the at least one ester oil in the preparation according to the invention is 0.1 to 10.0% by weight, preferably 0.3 to 6.0% by weight, particularly preferably 0.5 to 4.0% by weight .
  • Polyols can also be counted among the emollients. Polyols are distinguished by the presence of at least two hydroxyl groups. Polyols having 3 to 6 carbon atoms are preferred.
  • the preparation according to the invention particularly preferably contains propylene glycol, glycerol, sorbitol.
  • the at least one emollient selected from propylene glycol, glycerol and / or sorbitol is present with a content of 2.0 to 6.0% by weight, based on the total weight of the preparation.
  • the preparation according to the invention contains at least one thickener.
  • the viscosity and consistency of cosmetic preparations can be influenced.
  • Advantageous viscosity ranges can be set.
  • the consistency can be designed in such a way that corresponding products can be made available to consumer wishes.
  • thickening cleaning preparations for example electrolytes, in particular NaCl, alkanolamides, highly ethoxylated ethers and esters, polymeric thickeners and associative thickeners.
  • the preparation according to the invention contains at least one thickener which is selected from the group of highly ethoxylated ethers and / or esters.
  • This group of thickeners can also have a foam-boosting effect, they are then referred to as so-called “foam boosters”.
  • PEG-150 distearates PEG-120 methyl glucose dioleates, PEG-120 methyl glucose trioleates, PEG-160 sorbitan isostearates and PEG-150 pentaerythrityl tetrastates can be listed as examples. It is preferred if the preparation according to the invention contains PEG-150 pentaerythrityl tetrastearates.
  • the preparation according to the invention contains at least one thickener selected from the group of highly ethoxylated esters, the content is in a range from 0.01 to 0.4% by weight, preferably 0.02 to 0.3% by weight, based on its active content and the total weight of the preparation.
  • polymeric thickeners which are composed of monomer units which are present in a large number in the molecule. Methacrylic acid and acrylic acid and their derivatives are frequently used for the synthesis of polymeric thickeners. These polymers can be referred to as methacrylate or acrylate based. be net. It is advantageous according to the invention if the preparation of the present invention is free of methacrylate- or acrylate-based thickening polymers, with the proviso that polyquaternium-6, polyquaternium-7 and polyquaternium-53 are not included.
  • the preparation according to the invention can be preserved in the manner customary for cosmetic preparations.
  • the concentration of preservatives according to the invention is 0.05 to 3.3% by weight, preferably 0.1 to 2.6% by weight, based on the total weight of the preparation according to the invention.
  • the preservatives mentioned can each be contained individually or in suitable combinations in the preparation according to the invention.
  • Preservation with benzoic acid and / or a salt of benzoic acid, with salicylic acid and / or a salt of salicylic acid and / or with sorbic acid and / or a salt of sorbic acid is advantageous.
  • Preservation with sodium benzoate and / or sodium salicylate is particularly advantageous.
  • Benzoic acid, salicylic acid, sorbic acid and / or their salts are advantageously present with contents of 0.05 to 1.5% by weight, preferably 0.1 to 1.0% by weight, based on the total weight of the preparation.
  • the concentration information relates to the total amount of the advantageous preservative substances mentioned.
  • substances that are usually used to adjust the pH of the preparation according to the invention and to keep it stable.
  • These substances can advantageously be selected from the group of citric acid and lactic acid and / or from the group of aminomethylpropanol, sodium hydroxide solution, potassium hydroxide solution and triethanolamine.
  • the additives and auxiliaries common in cosmetics can be incorporated into the preparation if necessary, such as deodorizing substances, antiperspirants, insect repellents, vitamins, pigments with a coloring effect, flavoring agents, denaturants, perfumes, antioxidants, UV filter substances, sensor additives, active ingredients.
  • Pearlescent pigments belong to different chemical substance classes. Natural pearlescent pigments are, for example, "fish silver” (guanine / hypoxanthine mixed crystals from fish scales) or “mother-of-pearl” (ground mussel shells), monocrystalline pearlescent pigments are, for example, bismuth oxychloride (BiOCI) and layered substrates are, for example, mica / metal oxide.
  • Natural pearlescent pigments are, for example, "fish silver” (guanine / hypoxanthine mixed crystals from fish scales) or "mother-of-pearl” (ground mussel shells)
  • monocrystalline pearlescent pigments are, for example, bismuth oxychloride (BiOCI) and layered substrates are, for example, mica / metal oxide.
  • Pearlescent pigments are based, for example, on powdered pigments or castor oil dispersions of bismuth oxychloride and / or titanium dioxide and bismuth oxychloride and / or titanium dioxide on mica. It can also other substrates besides mica coated with other metal oxides, such as. B. silica and the like.
  • dialkyl ethers which are solid at 30 ° C. can be used as pearlescent agents and have, for example: the following formula: ROR ' .
  • R and R ' can be the same or different; straight-chain or branched, saturated or unsaturated alkyl radicals. These can consist of 12 to 30 carbon atoms, preferably 14 to 24 carbon atoms.
  • Acylated radicals consisting of a fatty acid chain with 8 to 30 carbon atoms can also be used.
  • Such compounds are, for example, ethylene glycol monostearate and ethylene glycol distearate.
  • Opacifiers can include, for example, sodium salts of a polymer made from styrene with a monomer consisting of acrylic acid, methacrylic acid or another olefin and one of their esters, e.g. INCI: Sodium Styrene / Acrylates Copolymer,
  • the preparation according to the invention is free from the pearlescent and opacifying agents mentioned.
  • the preparation according to the invention can be produced using all methods known to the person skilled in the art and suitable for this type of preparation. However, it is advantageous if the preparation according to the invention is produced in the following way:
  • Conditioners can also be added to the water phase if necessary.
  • the preparation according to the invention is stable over a longer period of time, the preparation was stored at 25 ° C. for 8 months. The viscosity and pH were determined at selected times.
  • the rating "ok” means no change in the general stability, no phase separation, no discoloration, no deposits, the opaque, white appearance remains.
  • the viscosity values disclosed in the present document were measured with the Rheomat R123 from ProRheo at 25 ° C.
  • the rotor of the device is immersed in the sample without bubbles up to the mark.
  • the measuring body 1 was used for the measurements. Further information on the Rheomat R 123 is published on the Internet, see:
  • the measured viscosity values fluctuate in the examined time interval by about 22%, this is in the usual range for such preparations.
  • the preparations are all characterized by a simple method of preparation, develop a rich, creamy foam and have an opaque, white appearance that is retained over the storage period.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
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  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

L'invention concerne une préparation nettoyante cosmétique moussante présentant un aspect opaque dû au fait que la préparation se présente sous la forme d'une émulsion.
PCT/EP2019/072081 2018-09-10 2019-08-19 Préparation nettoyante moussante à base d'une émulsion Ceased WO2020052913A1 (fr)

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EP19756347.1A EP3849502A1 (fr) 2018-09-10 2019-08-19 Préparation nettoyante moussante à base d'une émulsion

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DE102018215330.2 2018-09-10
DE102018215330.2A DE102018215330A1 (de) 2018-09-10 2018-09-10 Schäumende Reinigungszubereitung auf Basis einer Emulsion

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WO2020052913A1 true WO2020052913A1 (fr) 2020-03-19

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Cited By (1)

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CN112494392A (zh) * 2020-12-25 2021-03-16 彭氏(惠州)实业发展有限公司 一种清洁型水包油化妆品组合物及其制备方法

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WO2022136095A1 (fr) * 2020-12-21 2022-06-30 L'oreal Composition comprenant une émulsion de silicone, un polymère de (méth)acrylamide particulier, un polysaccharide cationique et un polymère d'alkyldiallylamine ou de dialkyldiallylammonium
FR3119768B1 (fr) * 2021-02-12 2025-07-18 Oreal Composition comprenant une émulsion de silicone, un polymère particulier de (méth)acrylamide, un polysaccharide cationique et un polymère d’alkyldiallylamine ou de dialkyldiallylammonium

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DE10107216A1 (de) 2001-02-16 2002-08-22 Schwarzkopf Gmbh Hans Wirkstoffkombination aus Kohlenwasserstoffen und Ölen in kosmetischen Mitteln
EP1366740A1 (fr) * 2002-05-31 2003-12-03 Beiersdorf AG Shampooing traitant opacifié
EP1393707A1 (fr) * 2002-08-17 2004-03-03 Beiersdorf AG Conmposition cosmétique pour nettoyer et soigner la peau
US20050143268A1 (en) * 2003-11-14 2005-06-30 The Procter & Gamble Company Personal care composition containing a cleansing phase and a benefit phase
WO2007104740A1 (fr) 2006-03-13 2007-09-20 Beiersdorf Ag Émulsion lavante sans silicone pour les cheveux
US20090257968A1 (en) * 2004-03-25 2009-10-15 Richard Walton Gels containing anionic surfactants and coupling agents
DE102015225005A1 (de) 2015-12-11 2017-06-14 Henkel Ag & Co. Kgaa Emulsionen enthaltend mindestens eine spezielle Konservierungsmittelkombination
DE102015225003A1 (de) 2015-12-11 2017-06-14 Henkel Ag & Co. Kgaa Emulsionen enthaltend mindestens drei voneinander verschiedene Konservierungsmittel
US20180116937A1 (en) * 2016-10-31 2018-05-03 L'oreal Cleansing compositions with conditioning properties

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DE102008036957A1 (de) * 2008-08-08 2010-02-11 Henkel Ag & Co. Kgaa Mattierungsadditiv für Blondierungen
DE102013226698A1 (de) * 2013-12-19 2015-06-25 Henkel Ag & Co. Kgaa Oxidationsfärbemittel mit natürlichem Pflegestoff

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Publication number Priority date Publication date Assignee Title
EP1072249A2 (fr) * 1999-07-26 2001-01-31 Beiersdorf AG Compositions cosmétiques et dermatologiques basées sur des émulsions huile-dans-eau
DE10107216A1 (de) 2001-02-16 2002-08-22 Schwarzkopf Gmbh Hans Wirkstoffkombination aus Kohlenwasserstoffen und Ölen in kosmetischen Mitteln
EP1366740A1 (fr) * 2002-05-31 2003-12-03 Beiersdorf AG Shampooing traitant opacifié
EP1393707A1 (fr) * 2002-08-17 2004-03-03 Beiersdorf AG Conmposition cosmétique pour nettoyer et soigner la peau
US20050143268A1 (en) * 2003-11-14 2005-06-30 The Procter & Gamble Company Personal care composition containing a cleansing phase and a benefit phase
US20090257968A1 (en) * 2004-03-25 2009-10-15 Richard Walton Gels containing anionic surfactants and coupling agents
WO2007104740A1 (fr) 2006-03-13 2007-09-20 Beiersdorf Ag Émulsion lavante sans silicone pour les cheveux
DE102015225005A1 (de) 2015-12-11 2017-06-14 Henkel Ag & Co. Kgaa Emulsionen enthaltend mindestens eine spezielle Konservierungsmittelkombination
DE102015225003A1 (de) 2015-12-11 2017-06-14 Henkel Ag & Co. Kgaa Emulsionen enthaltend mindestens drei voneinander verschiedene Konservierungsmittel
US20180116937A1 (en) * 2016-10-31 2018-05-03 L'oreal Cleansing compositions with conditioning properties

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112494392A (zh) * 2020-12-25 2021-03-16 彭氏(惠州)实业发展有限公司 一种清洁型水包油化妆品组合物及其制备方法

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