WO2009153281A1 - Composition - Google Patents

Composition Download PDF

Info

Publication number
WO2009153281A1
WO2009153281A1 PCT/EP2009/057517 EP2009057517W WO2009153281A1 WO 2009153281 A1 WO2009153281 A1 WO 2009153281A1 EP 2009057517 W EP2009057517 W EP 2009057517W WO 2009153281 A1 WO2009153281 A1 WO 2009153281A1
Authority
WO
WIPO (PCT)
Prior art keywords
waxes
composition
silicone
wax
polymer
Prior art date
Application number
PCT/EP2009/057517
Other languages
English (en)
Inventor
Colin Christopher David Giles
Anuchai Sinsawat
Original Assignee
Unilever Plc
Unilever N.V.
Hindustan Unilever Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to BRPI0909940A priority Critical patent/BRPI0909940A2/pt
Application filed by Unilever Plc, Unilever N.V., Hindustan Unilever Limited filed Critical Unilever Plc
Priority to CN200980122953.2A priority patent/CN102065830A/zh
Priority to AU2009259418A priority patent/AU2009259418A1/en
Priority to EA201170063A priority patent/EA201170063A1/ru
Priority to EP09765861A priority patent/EP2293769A1/fr
Priority to MX2010014069A priority patent/MX2010014069A/es
Priority to JP2011514030A priority patent/JP2011524876A/ja
Publication of WO2009153281A1 publication Critical patent/WO2009153281A1/fr

Links

Classifications

    • 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
    • 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
    • A61K8/31—Hydrocarbons
    • 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
    • A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
    • 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
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/12—Preparations containing hair conditioners
    • 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
    • A61K2800/54—Polymers characterized by specific structures/properties
    • A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5424—Polymers characterized by specific structures/properties characterized by the charge anionic

Definitions

  • the invention relates to an improved conditioning composition .
  • a hair conditioning composition comprising hydrophobically modified anionic polymer .
  • the hydrophobically-modified anionic polymer provides better rinse-off properties. This is particularly so when the composition is a conditioning mask composition.
  • the polymer is an acrylate or methacrylate polymer .
  • the hydrophobic modification comprises alkylation .
  • the alkyl group comprises from 6 to 30 carbons, more preferably from 16 to 28 and most preferably from 18 to 24 carbons.
  • a preferred polymer is sold by Rohm & Haas under the tradename Aculyn. The most preferred of which is Aculyn 28TM.
  • the polymer is present at from 0.01 to 5% wt . and more preferably from 0.05 to 1% wt .
  • composition according to any preceding claim comprising a structurant.
  • the structurant improves the feel of the product in the hand of the user.
  • the structurant used for "structuring" the composition according to the invention may be a natural or synthetic crystalline wax.
  • Mineral, animal or plant (vegetable) waxes are all described as natural waxes.
  • Synthetic waxes are described as those waxes that have been synthetically polymerized from raw materials or chemically modified natural waxes.
  • paraffin waxes which may be used are petroleum based waxes such as paraffins and microcrystalline wax. Chemically, both microcrystalline (MC) and paraffin waxes are very similar, consisting of long saturated hydrocarbon chains. Both types of waxes are separated from crude petroleum with the MC waxes typically having higher molecular weights. Paraffin wax is extracted from the high boiling fractions of crude petroleum during the refining process by cooling and filtering. Following a sweating process to remove remaining oil in the wax, the resulting paraffin wax typically has less than 0.5 % oil.
  • paraffin waxes are colourless or white and transparent. Paraffin waxes consist mainly of straight chain molecules with a small amount of branched- chain molecules mostly having branching near the end of the chains. As a result of the long, straight chains, paraffin wax has large, well-formed crystals. Molecular weights of paraffin waxes generally range from 360 to 420 (26 to 30 carbon atoms), although versions with longer chains (molecular weights up to 600) are available. Typical melting points are 126-134 0 F (52-57 0 C), the high molecular weight versions have melting points near 17O 0 F (77 0 C) . Paraffin waxes are brittle and the addition of oil, weakens the structure (lowers the tensile strength) .
  • Microcrystalline waxes differ from paraffin waxes in physical properties, chain structure and length, and in the process of manufacture. They are tougher, more flexible and have higher tensile strength and melting points than paraffin waxes. MC waxes have high affinity for oil which, when added, increases the wax plasticity. MC wax cannot be distilled without decomposition, and therefore is separated from the residual distillation fraction of crude petroleum by de-waxing processes involving recrystallization in organic solvents and centrifugation . Oil content varies with grade but is usually around 2 % to 12 %. MC waxes contain mostly branched-chain molecules located at random along the chain with some straight chains. Typical melting points are 145 to 195 0 F (63-91 0 C) . A high penetration number indicates flexibility of the wax, but flexibility is not a function of melting point.
  • mineral waxes such as montan wax, lignite wax, osocerite, ceresin, utah wax and peat wax.
  • Animal waxes can be obtained from such things as bees, insects or whales. These waxes include but are not limited to beeswax, Chinese wax, shellac wax, spermaceti and wool wax.
  • Beeswax for example, classified as an animal wax, is secreted by the honey bee to construct the honeycomb. The wax is harvested by melting the honeycomb and filtering away the wax.
  • Beeswax has melting points around 61-65 0 C, and is compatible with almost all waxes and oils.
  • Plant waxes can be derived from beans, leaves and berries. Plant or vegetable waxes can include bayberry, candelilla, carnauba, cotton, esparto, fir, Japan, ouricury, palm, rice- oil, sugar cane, ucuhuba and cocoa butter.
  • synthetic crystalline waxes which may be used are crystalline polymers such as polyethylene, polymethylene, chemically modified waxes, polymerized alpha olefins and synthetic animal waxes.
  • crystalline polymers such as polyethylene, polymethylene, chemically modified waxes, polymerized alpha olefins and synthetic animal waxes.
  • siliconyl beeswax may be used which is beeswax that has been chemically modified.
  • Penetration number values as reported by manufacturers using the standard test method for needle penetration of petroleum waxes of the American Society for Testing and Materials (ASTM D1321) .
  • the depth of penetration of needle in tenths of a millimeter (dmm) is measured with a penetrometer that applies a standard needle to the sample for 5 seconds under a load of 100 grams.
  • microcrystalline wax petrolatum also known as petrolatum or mineral jelly
  • microcrystalline wax petrolatum typically comprises about 90% by wt . of a natural mixture of microcrystalline waxes plus minor amounts of other impurities.
  • composition according to the invention may comprise any of a number of ingredients which are common to conditioning compositions .
  • compositions in accordance with the invention may also be formulated as conditioners for the treatment of hair (typically after shampooing) and subsequent rinsing.
  • Such a conditioner will comprise one or more conditioning surfactants which are cosmetically acceptable and suitable for topical application to the hair.
  • Suitable conditioning surfactants are selected from cationic surfactants, used singly or in admixture. Examples include quaternary ammonium hydroxides or salts thereof, e.g. chlorides .
  • Suitable cationic surfactants for use in hair conditioners of the invention include cetyltrimethylammonium chloride, behenyltrimethylammonium chloride, cetylpyridinium chloride, tetramethylammonium chloride, tetraethylammonium chloride, octyltrimethylairanonium chloride, dodecyltrimethylammonium chloride, hexadecyltrimethylairanonium chloride, octyldimethylbenzylammonium chloride, decyldimethylbenzylairanonium chloride, stearyldimethylbenzylammonium chloride, didodecyldimethy1ammonium chloride, dioctadecyldimethylammonium chloride, tallowtrimethylammonium chloride, cocotrimethylammonium chloride, and the corresponding hydroxides thereof.
  • cationic surfactants include those materials having the CTFA designations Quaternium-5, Quaternium-31 and Quaternium-18. Mixtures of any of the foregoing materials may also be suitable.
  • a particularly useful cationic surfactant for use in hair conditioners of the invention is cetyltrimethylammonium chloride, available commercially, for example as DEHYQUART, ex Henkel.
  • the level of cationic surfactant is preferably from 0.01 to 10%, more preferably 0.05 to 5%, most preferably 0.1 to 2% by weight of the composition .
  • Conditioners of the invention advantageously incorporate a fatty alcohol material.
  • fatty alcohol materials and cationic surfactants in conditioning compositions is believed to be especially advantageous, because this leads to the formation of a lamellar phase, in which the cationic surfactant is dispersed.
  • Representative fatty alcohols comprise from 8 to 22 carbon atoms, more preferably 16 to 20. Examples of suitable fatty alcohols include cetyl alcohol, stearyl alcohol and mixtures thereof. The use of these materials is also advantageous in that they contribute to the overall conditioning properties of compositions of the invention.
  • the level of fatty alcohol material in conditioners of the invention is conveniently from 0.01 to 10%, preferably from 0.1 to 5% by weight of the composition.
  • the weight ratio of cationic surfactant to fatty alcohol is suitably from 10:1 to 1:10, preferably from 4:1 to 1:8, optimally from 1:1 to 1:4.
  • Silicone is a particularly preferred ingredient in hair treatment compositions of the invention.
  • conditioners of the invention will preferably also comprise emulsified particles of silicone, for enhancing conditioning performance.
  • the silicone is insoluble in the aqueous matrix of the composition and so is present in an emulsified form, with the silicone present as dispersed particles.
  • Suitable silicones include polydiorganosiloxanes, in particular polydimethylsiloxanes which have the CTFA designation dimethicone. Also suitable for use compositions of the invention are polydimethyl siloxanes having hydroxyl end groups, which have the CTFA designation dimethiconol . Also suitable for use in compositions of the invention are silicone gums having a slight degree of cross-linking, as are described for example in WO 96/31188. These materials can impart body, volume and stylability to hair, as well as good wet and dry conditioning. The viscosity of the emulsified silicone itself (not the emulsion or the final hair conditioning composition) is typically at least 10,000 cst.
  • the viscosity of the silicone itself is preferably at least 60,000 cst, most preferably at least 500,000 cst, ideally at least 1,000,000 cst. Preferably the viscosity does not exceed 10 9 cst for ease of formulation .
  • Emulsified silicones for use in conditioners of the invention will typically have an average silicone particle size in the composition of less than 30, preferably less than 20, more preferably less than 10 microns. We have found that reducing the particle size generally improves conditioning performance. Most preferably the average silicone particle size of the emulsified silicone in the composition is less than 2 microns, ideally it ranges from 0.01 to 1 micron. Silicone emulsions having an average silicone particle size of ⁇ 0.15 microns are generally termed microemulsions .
  • Particle size may be measured by means of a laser light scattering technique, using a 2600D Particle Sizer from Malvern Instruments.
  • Suitable silicone emulsions for use in the invention are also commercially available in a pre-emulsified form.
  • Suitable pre-formed emulsions include emulsions DC2-1766, DC2-1784, and microemulsions DC2-1865 and DC2-1870, all available from Dow Corning. These are all emulsions/microemulsions of dimethiconol .
  • Cross-linked silicone gums are also available in a pre-emulsified form, which is advantageous for ease of formulation.
  • a preferred example is the material available from Dow Corning as DC X2- 1787, which is an emulsion of cross-linked dimethiconol gum.
  • a further preferred example is the material available from Dow Corning as DC X2-1391, which is a microemulsion of cross-linked dimethiconol gum.
  • a further preferred class of silicones for inclusion in conditioners of the invention are amino functional silicones.
  • amino functional silicone is meant a silicone containing at least one primary, secondary or tertiary amine group, or a quaternary ammonium group.
  • Suitable amino functional silicones include:
  • x and y are numbers depending on the molecular weight of the polymer, generally such that the molecular weight is between about 5,000 and 500,000.
  • G is selected from H, phenyl, OH or Ci-8 alkyl, e.g. methyl; a is 0 or an integer from 1 to 3, preferably 0; b is 0 or 1, preferably 1; m and n are numbers such that (m + n) can range from 1 to 2000, preferably from 50 to 150; m is a number from 1 to 2000, preferably from 1 to 10; n is a number from 0 to 1999, preferably from 49 to 149, and
  • R is a monovalent radical of formula -C q H2 q L in which q is a number from 2 to 8 and L is an aminofunctional group selected from the following:
  • R " is selected from H, phenyl, benzyl, or a saturated monovalent hydrocarbon radical, e.g. Ci-20 alkyl, and;
  • A is a halide ion, e.g. chloride or bromide.
  • Suitable amino functional silicones corresponding to the above formula include those polysiloxanes termed “trimethylsilylamodimethicone” as depicted below, and which are sufficiently water insoluble so as to be useful in compositions of the invention:
  • x + y is a number from about 50 to about 500, and wherein R is an alkylene group having from 2 to 5 carbon atoms.
  • the number x + y is in the range of from about 100 to about 300.
  • R 1 and R 10 may be the same or different and may be independently selected from H, saturated or unsaturated long or short chain alk(en)yl, branched chain alk(en)yl and C5-C8 cyclic ring systems;
  • R 2 thru' R 9 may be the same or different and may be independently selected from H, straight or branched chain lower alk(en)yl, and C 5 -Cs cyclic ring systems; n is a number within the range of about 60 to about 120, preferably about 80, and
  • X ⁇ is preferably acetate, but may instead be for example halide, organic carboxylate, organic sulphonate or the like. Suitable quaternary silicone polymers of this class are described in EP-A-O 530 974.
  • Amino functional silicones suitable for use in conditioners of the invention will typically have a mole % amine functionality in the range of from about 0.1 to about 8.0 mole %, preferably from about 0.1 to about 5.0 mole %, most preferably from about 0.1 to about 2.0 mole %. In general the amine concentration should not exceed about 8.0 mole % since we have found that too high an amine concentration can be detrimental to total silicone deposition and therefore conditioning performance.
  • the viscosity of the amino functional silicone is not particularly critical and can suitably range from about 100 to about 500,000 cst.
  • amino functional silicones suitable for use in the invention are the aminosilicone oils DC2-8220, DC2-8166, DC2-8466, and DC2-8950-114 (all ex Dow Corning), and GE 1149-75, (ex General Electric Silicones) .
  • emulsions of amino functional silicone oils with non ionic and/or cationic surfactant are also suitable.
  • Such pre-formed emulsions will have an average amino functional silicone particle size in the composition of less than 30, preferably less than 20, more preferably less than 10 microns. Again, we have found that reducing the particle size generally improves conditioning performance. Most preferably the average amino functional silicone particle size in the composition is less than 2 microns, ideally it ranges from 0.01 to 1 micron. Silicone emulsions having an average silicone particle size of ⁇ 0.15 microns are generally termed microemulsions .
  • Pre-formed emulsions of amino functional silicone are also available from suppliers of silicone oils such as Dow Corning and General Electric. Specific examples include DC929 Cationic Emulsion, DC939 Cationic Emulsion, and the non-ionic emulsions DC2-7224, DC2-8467, DC2-8177 and DC2-8154 (all ex Dow Corning) .
  • quaternary silicone polymer useful in the present invention is the material K3474, ex Goldschmidt.
  • the total amount of silicone incorporated into compositions of the invention depends on the level of conditioning desired and the material used.
  • a preferred amount is from 0.01 to about 10% by weight of the total composition although these limits are not absolute.
  • the lower limit is determined by the minimum level to achieve conditioning and the upper limit by the maximum level to avoid making the hair and/or skin unacceptably greasy.
  • a total amount of silicone of from 0.3 to 5%, preferably 0.5 to 3%, by weight of the total composition is a suitable level.
  • ingredients may include viscosity modifiers, preservatives, colouring agents, polyols such as glycerine and polypropylene glycol, chelating agents such as EDTA, antioxidants such as vitamin E acetate, fragrances, antimicrobials and sunscreens.
  • viscosity modifiers preservatives, colouring agents, polyols such as glycerine and polypropylene glycol, chelating agents such as EDTA, antioxidants such as vitamin E acetate, fragrances, antimicrobials and sunscreens.
  • compositions of this invention also contain adjuvants suitable for hair care.
  • adjuvants suitable for hair care Generally such 10 ingredients are included individually at a level of up to
  • Suitable hair care adjuvants are:
  • amino acids such as amino acids and sugars.
  • suitable amino acids include arginine, cysteine, glutamine, glutamic acid, isoleucine, leucine, methionine, serine and valine, and/or precursors and derivatives thereof.
  • the amino acids may be added singly, in mixtures,
  • amino acids 20 or in the form of peptides, e.g. di- and tripeptides.
  • the amino acids may also be added in the form of a protein hydrolysate, such as a keratin or collagen hydrolysate.
  • Suitable sugars are glucose, dextrose and fructose. These may be added singly or in the form of, e.g. fruit extracts.
  • hair fibre benefit agents examples are: ceramides, for moisturising the fibre and maintaining cuticle integrity. Ceramides are available by extraction from natural sources, or as synthetic ceramides and
  • a preferred ceramide is Ceramide II, ex Quest. Mixtures of ceramides may also be suitable, such as Ceramides LS, ex Laboratoires Serobi unanimouss .
  • free fatty acids for cuticle repair and damage prevention.
  • branched chain fatty acids such as 18-methyleicosanoic acid and other homologues of this series, straight chain fatty acids such as stearic, myristic and palmitic acids, and unsaturated fatty acids such as oleic acid, linoleic acid, linolenic acid and arachidonic acid.
  • a preferred fatty acid is oleic acid.
  • the fatty acids may be added singly, as mixtures, or in the form of blends derived from extracts of, e.g. lanolin.
  • a conditioning gel phase which comprises a cationic surfactant and a fatty material and, separately forming a solution of the hydrophobically modified polymer, optionally with a cationic surfactant, which, if present, is added to the water first.
  • the two mixtures are then added to one another before the remaining ingredients are added to form the conditioning composition .
  • the extra ingredients include perfumes, thickeners, preservatives, colours and conditioning silicones .
  • Formulation according to the invention It is made by heating approximately 35% wt . of the water to 65-70 0 C prior to addition of stearmidopropyl dimethylamine . Continue mixing until product completely dissolved.
  • Composition A is a composition according to the invention and is made by a process similar to that described in Example 1.
  • Composition B is a comparative composition which does not comprise any of the hydrophobically modified polymer .
  • compositions A and B were compared in a head to head comparison where the assessment made by an expert panel was ease of rinsing. Out of the 12 expert assessors, 11 considered composition A to provide better ease of rinse.

Landscapes

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

Abstract

composition de traitement capillaire comprenant un polymère anionique modifié au plan hydrophobique.
PCT/EP2009/057517 2008-06-20 2009-06-17 Composition WO2009153281A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
BRPI0909940A BRPI0909940A2 (pt) 2008-06-20 2009-02-17 composição de condicionamento do cabelo
CN200980122953.2A CN102065830A (zh) 2008-06-20 2009-06-17 组合物
AU2009259418A AU2009259418A1 (en) 2008-06-20 2009-06-17 Composition
EA201170063A EA201170063A1 (ru) 2008-06-20 2009-06-17 Композиция
EP09765861A EP2293769A1 (fr) 2008-06-20 2009-06-17 Composition
MX2010014069A MX2010014069A (es) 2008-06-20 2009-06-17 Composicion.
JP2011514030A JP2011524876A (ja) 2008-06-20 2009-06-17 組成物

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP08158658.8 2008-06-20
EP08158658 2008-06-20

Publications (1)

Publication Number Publication Date
WO2009153281A1 true WO2009153281A1 (fr) 2009-12-23

Family

ID=39954259

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2009/057517 WO2009153281A1 (fr) 2008-06-20 2009-06-17 Composition

Country Status (11)

Country Link
EP (1) EP2293769A1 (fr)
JP (1) JP2011524876A (fr)
KR (1) KR20110036047A (fr)
CN (1) CN102065830A (fr)
AR (1) AR072176A1 (fr)
AU (1) AU2009259418A1 (fr)
BR (1) BRPI0909940A2 (fr)
EA (1) EA201170063A1 (fr)
MX (1) MX2010014069A (fr)
TW (1) TW201000145A (fr)
WO (1) WO2009153281A1 (fr)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012150260A1 (fr) * 2011-05-04 2012-11-08 Unilever Plc Composition de soin pour les cheveux comprenant un polymère anionique à modification hydrophobe et une méthocellulose
WO2012150259A1 (fr) * 2011-05-04 2012-11-08 Unilever Plc Composition
US9556405B2 (en) 2012-11-29 2017-01-31 Conopco, Inc. Polymer structured aqueous detergent compositions
WO2018228899A1 (fr) 2017-06-15 2018-12-20 Unilever Plc Composition de conditionnement de cheveux pour un rinçage amélioré
WO2018228900A1 (fr) 2017-06-15 2018-12-20 Unilever Plc Composition de soin capillaire ayant des propriétés de rinçage améliorées
WO2018228898A1 (fr) 2017-06-15 2018-12-20 Unilever Plc Composition capillaire ayant des propriétés de rinçage améliorées
WO2019233858A1 (fr) * 2018-06-07 2019-12-12 Unilever Plc Procédé

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102727395B (zh) * 2011-04-12 2017-08-08 拜尔斯道夫股份有限公司 可雾化的毛发定型组合物
JP6211436B2 (ja) * 2014-02-28 2017-10-11 株式会社マンダム リンス剤

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5656257A (en) * 1995-04-28 1997-08-12 Electronics Hair Styling, Inc. Shampoo and conditioning composition
US5827920A (en) * 1995-06-30 1998-10-27 Shiseido Company, Ltd. Emulsion composition
WO2000021495A1 (fr) * 1998-10-09 2000-04-20 Colgate-Palmolive Company Compositions de soins capillaires volumatrices contenant des siloxysilicates
WO2000040211A1 (fr) * 1999-01-04 2000-07-13 The Procter & Gamble Company Composition pour le conditionnement des cheveux comprenant un copolymere acide carboxylique/carboxylate ainsi que des particules visibles et cassables
US20050123573A1 (en) * 2003-12-08 2005-06-09 Spadini Alessandro L. Stable nonaqueous reactive skin care and cleansing compositions having a continuous and a discontinuous phase
EP1563831A1 (fr) * 2004-10-26 2005-08-17 Shiseido Co., Ltd. Preparation pour la peau a usage externe
US20060193789A1 (en) * 2002-10-25 2006-08-31 Foamix Ltd. Film forming foamable composition
DE102005022021A1 (de) * 2005-05-12 2006-11-16 Basf Ag Isoalkangemisch, dessen Herstellung und Verwendung
US20070225196A1 (en) * 2006-03-22 2007-09-27 The Procter & Gamble Company Aerosol product comprising a foaming concentrate composition comprising particulate materials

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5656257A (en) * 1995-04-28 1997-08-12 Electronics Hair Styling, Inc. Shampoo and conditioning composition
US5827920A (en) * 1995-06-30 1998-10-27 Shiseido Company, Ltd. Emulsion composition
WO2000021495A1 (fr) * 1998-10-09 2000-04-20 Colgate-Palmolive Company Compositions de soins capillaires volumatrices contenant des siloxysilicates
WO2000040211A1 (fr) * 1999-01-04 2000-07-13 The Procter & Gamble Company Composition pour le conditionnement des cheveux comprenant un copolymere acide carboxylique/carboxylate ainsi que des particules visibles et cassables
US20060193789A1 (en) * 2002-10-25 2006-08-31 Foamix Ltd. Film forming foamable composition
US20050123573A1 (en) * 2003-12-08 2005-06-09 Spadini Alessandro L. Stable nonaqueous reactive skin care and cleansing compositions having a continuous and a discontinuous phase
EP1563831A1 (fr) * 2004-10-26 2005-08-17 Shiseido Co., Ltd. Preparation pour la peau a usage externe
DE102005022021A1 (de) * 2005-05-12 2006-11-16 Basf Ag Isoalkangemisch, dessen Herstellung und Verwendung
US20070225196A1 (en) * 2006-03-22 2007-09-27 The Procter & Gamble Company Aerosol product comprising a foaming concentrate composition comprising particulate materials

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012150260A1 (fr) * 2011-05-04 2012-11-08 Unilever Plc Composition de soin pour les cheveux comprenant un polymère anionique à modification hydrophobe et une méthocellulose
WO2012150259A1 (fr) * 2011-05-04 2012-11-08 Unilever Plc Composition
JP2014513111A (ja) * 2011-05-04 2014-05-29 ユニリーバー・ナームローゼ・ベンノートシヤープ 疎水的に修飾されたアニオン性ポリマーおよびメチルセルロースを含むヘアケア組成物
EA026698B1 (ru) * 2011-05-04 2017-05-31 Унилевер Н.В. Композиция для ухода за волосами, содержащая гидрофобно-модифицированный анионный полимер и метилцеллюлозу
US9556405B2 (en) 2012-11-29 2017-01-31 Conopco, Inc. Polymer structured aqueous detergent compositions
WO2018228899A1 (fr) 2017-06-15 2018-12-20 Unilever Plc Composition de conditionnement de cheveux pour un rinçage amélioré
WO2018228900A1 (fr) 2017-06-15 2018-12-20 Unilever Plc Composition de soin capillaire ayant des propriétés de rinçage améliorées
WO2018228898A1 (fr) 2017-06-15 2018-12-20 Unilever Plc Composition capillaire ayant des propriétés de rinçage améliorées
EP3638375B1 (fr) 2017-06-15 2022-06-22 Unilever IP Holdings B.V. Composition capillaire présentant de meilleures propriétés de rinçage
WO2019233858A1 (fr) * 2018-06-07 2019-12-12 Unilever Plc Procédé

Also Published As

Publication number Publication date
BRPI0909940A2 (pt) 2015-10-20
EA201170063A1 (ru) 2011-06-30
AR072176A1 (es) 2010-08-11
JP2011524876A (ja) 2011-09-08
KR20110036047A (ko) 2011-04-06
TW201000145A (en) 2010-01-01
MX2010014069A (es) 2011-02-23
CN102065830A (zh) 2011-05-18
EP2293769A1 (fr) 2011-03-16
AU2009259418A1 (en) 2009-12-23

Similar Documents

Publication Publication Date Title
EP2293769A1 (fr) Composition
WO2009153280A1 (fr) Composition
AU739034B2 (en) Hair conditioning compositions
JP7278973B2 (ja) 改善されたリンス特性を有するヘアコンディショニング組成物
US20090041701A1 (en) Hair care composition
WO2018211485A1 (fr) Compositions d'après-shampooing à dépôt accru de microcapsules de polyacrylate
EP2296758B1 (fr) Composition après-shampooing comprenant trois silicones
US20090041713A1 (en) Hair Care Composition
EP2605743B1 (fr) Composition de soin capillaire
KR102485259B1 (ko) 모발 상태 개선용 액상 지질 복합 조성물
WO2014005821A2 (fr) Prémélange et composition
WO2010102891A2 (fr) Composition
US20190091115A1 (en) Conditioner compositions with polyacrylate microcapsules having improved long-lasting odor benefit
DE69834423T2 (de) Haarpflegezusammensetzung
CN111093605A (zh) 整发剂组合物
CN110769806A (zh) 用于改善的冲洗的毛发调理组合物
US20090044822A1 (en) Hair care composition

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200980122953.2

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 09765861

Country of ref document: EP

Kind code of ref document: A1

DPE1 Request for preliminary examination filed after expiration of 19th month from priority date (pct application filed from 20040101)
WWE Wipo information: entry into national phase

Ref document number: 2009765861

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2691/MUMNP/2010

Country of ref document: IN

Ref document number: MX/A/2010/014069

Country of ref document: MX

WWE Wipo information: entry into national phase

Ref document number: 2009259418

Country of ref document: AU

Ref document number: 2011514030

Country of ref document: JP

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 20117001351

Country of ref document: KR

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 201170063

Country of ref document: EA

ENP Entry into the national phase

Ref document number: 2009259418

Country of ref document: AU

Date of ref document: 20090617

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: PI0909940

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20101216