WO2000006095A1 - Compositions pour le soin des cheveux - Google Patents

Compositions pour le soin des cheveux Download PDF

Info

Publication number
WO2000006095A1
WO2000006095A1 PCT/US1998/015850 US9815850W WO0006095A1 WO 2000006095 A1 WO2000006095 A1 WO 2000006095A1 US 9815850 W US9815850 W US 9815850W WO 0006095 A1 WO0006095 A1 WO 0006095A1
Authority
WO
WIPO (PCT)
Prior art keywords
hair
hair care
cationic
compositions
silicone
Prior art date
Application number
PCT/US1998/015850
Other languages
English (en)
Inventor
Chantelle Mary Mccann
Anthony Mcmeekin
Graham Neil Mckelvey
Wendy Victoria Jane Young
Original Assignee
The Procter & Gamble Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to PCT/US1998/015850 priority Critical patent/WO2000006095A1/fr
Priority to AU87615/98A priority patent/AU8761598A/en
Priority to CN 99809931 priority patent/CN1313747A/zh
Priority to BR9912544-7A priority patent/BR9912544A/pt
Priority to PCT/US1999/006116 priority patent/WO2000006104A1/fr
Priority to AU33592/99A priority patent/AU3359299A/en
Priority to EP99914963A priority patent/EP1100439A1/fr
Priority to JP2000561961A priority patent/JP2003521450A/ja
Priority to CA002336680A priority patent/CA2336680A1/fr
Publication of WO2000006095A1 publication Critical patent/WO2000006095A1/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
    • 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
    • A61K8/8147—Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; 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
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/25—Silicon; Compounds 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
    • A61K8/8152—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
    • 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
    • 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

Definitions

  • the present invention relates to hair care compositions.
  • hair care compositions which are easy to spread through the hair and give improved conditioning and shine with reduced feelings of tackiness and greasiness.
  • Hair is often subjected to a wide variety of insults that can cause damage. These include shampooing, rinsing, drying, heating, combing, styling, perming, colouring, exposure to the elements etc. Thus the hair is often in a dry, rough, lusterless or frizzy condition due to abrasion of the hair surface and removal of the hair's natural oils and other natural conditioning and moisturizing components.
  • Leave-on hair care formulations provide added advantages over the other approaches. For example, leave-on formulations are more cost effective and work for a longer duration because the conditioning ingredients remain on the hair. They are more convenient because the consumer can use the product at any time and does not have to wait to rinse the product. Also, the product may be applied to the parts of the hair most in need of the conditioning benefits.
  • conditioning benefit is provided through the use of hair conditioning agents such as cationic surfactants, cationic polymers, silicone conditioning agents, hydrocarbon and other organic oils and solid aliphatics such as fatty alcohols.
  • hair conditioning agents such as cationic surfactants, cationic polymers, silicone conditioning agents, hydrocarbon and other organic oils and solid aliphatics such as fatty alcohols.
  • These conditioning agents are well known in the art. See, for example, WO-A-97/35542, WO-A-97/35545, WO-A-97/35546, all of which describe the use of conditioning agents in shampoo compositions.
  • these conditioning agents are deposited on the hair fibres and cause the hair to feel smooth and appear shiny.
  • the compositions should be easy to work through the hair to ensure that the agents are deposited fairly evenly along the hair shaft.
  • compositions, especially leave-on compositions where there is no rinsing step are often difficult to spread and can deposit too much conditioning agent in an uneven manner. This causes the hair to develop a dirty, coated feel and leaves the hair limp and without body. This is particularly noticeable when the compositions are used repeatedly and when the hair is not washed daily. It is therefore desirable to formulate compositions comprising as little conditioning agent as possible to achieve the desired benefits while ensuring that the agent is deposited as evenly as possible along the hair shaft.
  • polysiloxane resins could be used as hair conditioning agents.
  • GB-A-2,297,757 incorporated by reference herein, describes low viscosity organofunctionalised siloxysilicates and gives examples of their use in a hair care compositions.
  • this reference does not address the problem of providing hair care compositions that give shine and conditioning benefits and are easy to work through the hair but do not cause the hair to feel excessively tacky or greasy.
  • hair care compositions that are easy to disperse and deliver good conditioning and shine benefits with reduced tackiness are provided by combining polysiloxane resin, wherein at least one substituent group of the resin possesses delocalised electrons, with a viscosity modifier.
  • a leave-on hair care composition comprising:
  • compositions of the present invention are easy to spread through the hair and provide good conditioning and shine benefits with reduced feelings of tackiness and greasiness.
  • the hair care compositions of the present invention comprise two main elements, a polysiloxane resin, wherein at least one substituent group of the resin possesses delocalised electrons, and viscosity modifiers. These elements will be described in more detail below.
  • tacky and tackiness means the adhesive feeling of the hair after the application of some hair care compositions.
  • leave-on means a hair care composition that is intended to be used without a rinsing step. Therefore, leave-on compositions will generally be left on the hair until the consumer next washes their hair as part of their cleansing regimen. Leave-on will generally comprise less than about 5% of anionic surfactant and will generally comprise less than 5% of non-ionic surfactant.
  • compositions of the present invention comprise polysiloxane resin, wherein at least one substituent group of the resin possesses delocalised electrons.
  • the hair care compositions herein will generally comprise from about 0.001% to about 10%, preferably from about 0.005% to about 5%, more preferably from about 0.01% to about 2%, even more preferably from about 0.1% to about 1%, by weight, of polysiloxane resin.
  • Polysiloxane resins are highly crosslinked polymeric siloxane systems.
  • the crosslinking is introduced through the incorporation of trifunctional and tetrafunctional silanes with monofunctional or difunctional, or both, silanes during manufacture of the silicone resin.
  • the degree of crosslinking that is required in order to result in a silicone resin will vary according to the specific silane units incorporated into the silicone resin.
  • silicone materials which have a sufficient level of trifunctional and tetrafunctional siloxane monomer units (and hence, a sufficient level of crosslinking) such that they dry down to a rigid, or hard, film are considered to be silicone resins.
  • the ratio of oxygen atoms to silicon atoms is indicative of the level of crosslinking in a particular silicone material.
  • Silicone materials which have at least about 1.1 oxygen atoms per silicon atom will generally be silicone resins herein.
  • the ratio of oxygen:silicon atoms is at least about 1.2:1.0.
  • Silanes used in the manufacture of silicone resins include monomethyl, dimethyl, trimethyl, monophenyl, diphenyl, methylphenyl, ethylphenyl, propylphenyl, monovinyl, and methylvinylchlorosilanes, and tetrachlorosilane.
  • the polysiloxane resin for use herein must have at least one substituent group possessing delocalised electrons.
  • This substituent can be selected from alkyl, aryl, alkoxy, alkaryl, arylalkyl arylalkoxy, alkaryloxy, and combinations thereof.
  • Preferred are aryl, arylalkyl and alkaryl substituents. More preferred are alkaryl and arylalkyl substituents. Even more preferred are alkaryl substituents, particularly 2-phenyl propyl.
  • the resins herein will also generally have other substituents without delocalised electrons.
  • Such other substituents can include hydrogen, hydroxyl, alkyl, alkoxy, amino functionalities and mixtures thereof.
  • alkyl substituents especially methyl substituents. Therefore, particularly preferred for use herein is dimethyl (2-phenylpropyl) silyl ester.
  • aryl means a functionality containing one or more homocyclic or heterocyclic rings.
  • the aryl functionalities herein can be unsubstituted or substituted and generally contain from 3 to 16 carbon atoms.
  • Preferred aryl groups include, but are not limited to, phenyl, naphthyl, cyclopentadienyl, anthracyl, pyrene, pyridine, pyrimidine
  • alkyl means a saturated or unsaturated, substituted or unsubstituted, straight or branched-chain, hydrocarbon having from 1 to 10 carbon atoms, preferably 1 to 4 carbon atoms.
  • alkyl therefore includes alkenyls having from 2 to 8, preferably 2 to 4, carbons and alkynyls having from 2 to 8, preferably 2 to 4, carbons.
  • Preferred alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, and butyl. More preferred are methyl, ethyl and propyl.
  • alkaryl means a substituent comprising an alkyl moiety and an aryl moiety wherein the alkyl moiety is bonded to the siloxane resin.
  • arylalkyl means a substituent comprising an aryl moiety and an alkyl moiety wherein the aryl moiety is bonded to the siloxane resin.
  • Silicone materials and silicone resins in particular, can conveniently be identified according to a shorthand nomenclature system well known to those skilled in the art as "MDTQ" nomenclature. Under this system, the silicone is described according to presence of various siloxane monomer units which make up the silicone. Briefly, the symbol M denotes the monofunctional unit (CHs SiOrj.s; D denotes the difunctional unit (CH ⁇ SiO; T denotes the trifunctional unit
  • the molar ratios of the various units either in terms of subscripts to the symbols indicating the total number of each type of unit in the silicone (or an average thereof) or as specifically indicated ratios in combination with molecular weight complete the description of the silicone material under the MDTQ system.
  • Preferred polysiloxane resins for use herein are M'Q resins, more preferred are M' 6 Q 3 , M' 8 Q 4 and M' 10 Q 5 , M' 12 Q 6 resins and mixtures thereof.
  • Preferred M'Q resins are those which have at least one group containing delocalised electrons substituted on each M' functionality. More preferred are resins where the other substituent groups are alkyl, especially methyl.
  • the polysiloxane resins for use herein will preferably have a viscosity of less than about 5000 mm 2 s "1 , more preferably less than about 2000 mmV, even more preferably less than about 1000 mmV, even more still preferably less than about 600 mmV, at 25°C.
  • the viscosity can be measured by means of a Cannon-Fenske Routine Viscometer (ASTM D-445)
  • compositions of the present invention comprise a viscosity modifier.
  • Any viscosity modifier suitable for use in hair care compositions may be used herein.
  • the viscosity modifier will comprise from about 0.01% to about 10%, preferably from about 0.05% to about 5%, more preferably from about 0.1% to about 3%, by weight, of the total composition.
  • suitable viscosity modifiers can be found in the CTFA International Cosmetic Ingredient Dictionary and Handbook, 7th edition, edited by Wenninger and McEwen, (The Cosmetic, Toiletry, and Fragrance Association, Inc., Washington, D.C., 1997), herein incorporated by reference.
  • Suitable viscosity modifiers for use herein include shear sensitive viscosity modifiers.
  • shear sensitive viscosity modifiers means viscosity modifiers that can form compositions whose viscosity decreases at low shear rates.
  • Shear rate (s 1 ) can be defined as the ratio of the velocity (ms 1 ) of material to its distance from a stationary object (m). Shear rates of less than about 250s 1 can be thought of as "low shear rates”.
  • shear sensitive viscosity modifiers suitable for use in hair care may be used herein
  • preferred for use herein are viscosity modifiers which form compositions whose viscosity decreases at a shear rate of less than about 100s 1 , more preferably less than about 50s "1 .
  • preferred shear sensitive viscosity modifiers are those which can form compositions whose viscosity decreases by more than about 30%, preferably more than about 50%, more preferably more than about 70%, even more preferably more than about 80% at a shear rate of 50s 1 .
  • Preferred viscosity modifiers for use herein are those which form compositions whose viscosity is also sensitive to the electrolyte concentration in the aqueous phase, known hereafter as "salt sensitive viscosity modifiers". Background material on the properties of salt sensitive viscosity modifiers can be found in American Chemical Society Symposium Series (1991), Vol. 462, pp101-120, incorporated herein by reference. Any salt sensitive viscosity modifier suitable for use in hair care compositions may be used herein.
  • suitable viscosity modifiers include, but are not limited to, synthetic hectorites, carboxylic anionic polymers/copolymers and carboxylic anionic cross- linked polymers/ copolymers. Preferred for use herein are carboxylic anionic cross-linked polymers and copolymers. More preferred are carboxylic anionic cross-linked copolymers.
  • the synthetic hectorites useful herein are synthetic layered silicates such as sodium-magnesium silicate.
  • suitable synthetic hectorites include those available from Laporte Pic, United Kingdom under the trade name Laponite.
  • the carboxylic anionic copolymers useful herein can be hydrophobically-modified cross-linked copolymers of carboxylic acid and alkyl carboxylate, and have an amphiphilic property.
  • These carboxylic anionic copolymers are obtained by copolymerising 1) a carboxylic acid monomer such as acrylic acid, methacrylic acid, maleic acid, maleic anhydride, itaconic acid, fumaric acid, crotonic acid, or ⁇ -chloroacrylic acid, 2) a carboxylic ester having an alkyl chain of from 1 to about 30 carbons, and preferably 3) a crosslinking agent of the following formula:
  • R ⁇ is a hydrogen or an alkyl group having from about 1 to about 30 carbons
  • Y 1 independently, is oxygen, CH20, COO, OCO,
  • R 2 is a hydrogen or an alkyl group having from about 1 to about 30 carbons; and Y 2 is selected from (CH2)m", (CH2CH2 ⁇ ) m » j or (CH2CH2CH2 ⁇ ) m » wherein m" is an integer of from 1 to about 30.
  • Suitable carboxylic anionic copolymers herein are acrylic acid/alkyl acrylate copolymers having the following formula:
  • R 2 independently, is a hydrogen or an alkyl of 1 to 30 carbons wherein at least one of R 2 is a hydrogen, R 1 is as defined above, n, n', m and m' are integers in which n+n'+m+m' is from about 40 to about 100, n" is an integer of from 1 to about 30, and P is defined so that the copolymer has a molecular weight of about 5000 to about 3,000,000.
  • Neutralizing agents may be included to neutralize the carboxylic anionic copolymers herein.
  • neutralizing agents include sodium hydroxide, potassium hydroxide, ammonium hydroxide, monethanolamine, diethanolamine, triethanolamine, diisopropanolamine, aminomethylpropanol, tromethamine, tetrahydroxypropyl ethylenediamine, and mixtures thereof.
  • Non-limiting examples of suitable carboxylic anionic viscosity modifiers can be found in U.S. Pat. Nos. 3,940,351 ; 5,288,814; 5,349,030; 5,373,044 and 5,468,797, all of which are incorporated herein by reference.
  • Examples of carboxylic anionic viscosity modifiers include those available from B.F. Goodrich, Cleveland, OH, USA under the trade names Pemulen TR-1 , Pemulen TR-2, Carbopol 980, Carbopol 981 , Carbopol ETD- 2020, Carbopol ETD-2050 and Carbopol Ultrez 10.
  • Preferred are Carbopol ETD- 2020, Carbopol ETD-2050 and Carbopol Ultrez 10, especially Carbopol Ultrez 10.
  • Particularly preferred viscosity modifiers for use herein from the viewpoint of improving spreadability, reducing tack and improving shine are carboxylic anionic viscosity modifiers such as Carbopol Ultrez 10.
  • the hair care compositions of the present invention can further comprise a number of optional ingredients. Some non-limiting examples of these optional ingredients are given below.
  • compositions of the present invention may optionally include an additional silicone conditioning component.
  • the silicone conditioning component may comprise volatile silicone, nonvolatile silicone, or mixtures thereof. Typically, if volatile silicones are present, it will be incidental to their use as a solvent or carrier for commercially available forms of nonvolatile silicone materials ingredients, such as silicone gums and resins. Preferably the silicone is nonvolatile, however volatile silicones are not excluded from use herein.
  • nonvolatile refers to silicone material with little or no significant vapour pressure under ambient conditions, as is understood by those in the art. Boiling point under one atmosphere (atm) will preferably be at least about 250°C, more preferably at least about 275°C, most preferably at least about 300°C. Vapour pressure is preferably about 0.2mm Hg at 25°C or less, preferably about 0.1mm Hg at 25°C or less.
  • Silicone fluid for use in the present compositions include silicone oils which are flowable silicone materials with a viscosity of less than 1 ,000,000 mm 2 s "1 , preferably between about 5 and 1 ,000,000 mmV, more preferably between about 10 and about 600,000 mmV, more preferably between about 10 and about 500,000 mmV, most preferably between 10 and 350,000 mmV at 25°C.
  • the viscosity can be measured by means of a glass capillary viscometer as set forth in Dow Corning Corporate Test Method CTM0004, July 20, 1970.
  • Suitable silicone oils include polyalkyl siloxanes, polyaryl siloxanes, polyarylalkyl siloxanes, polyalkaryl siloxanes, polyether siloxane copolymers, and mixtures thereof. Other insoluble, nonvolatile silicone fluids having conditioning properties can also be used.
  • Silicone oils for use in the composition include polyalkyl or polyaryl siloxanes which conform to following formula:
  • R is aliphatic, preferably alkyl or alkenyl, or aryl
  • R can be substituted or unsubstituted
  • x is an integer from 1 to about 8,000.
  • Suitable unsubstituted R groups include alkoxy, aryloxy, alkaryl, arylalkyl, alkamino, and ether- substituted, hydroxyl-substituted, and halogen-substituted aliphatic and aryl groups.
  • Suitable R groups also include cationic amines and quaternary ammonium groups.
  • the aliphatic or aryl groups substituted on the siloxane chain may have any structure as long as the resulting silicones remain fluid at room temperature, are hydrophobic, are neither irritating, toxic nor otherwise harmful when applied to the hair, are compatible with the other components of the herein described hair care compositions, are chemically stable under normal use and storage conditions, are insoluble in the compositions of the present invention and are capable of conditioning the hair.
  • the two R groups on the silicon atom of each monomeric silicone unit may represent the same group or different groups.
  • the two R groups represent the same group.
  • Preferred alkyl and alkenyl substituents are C1-C5 alkyls and alkenyls, more preferably from C1-C4, most preferably from C-1-C2.
  • the aliphatic portions of other alkyl-, alkenyl-, or alkynyl-containing groups can be straight or branched chains and preferably have from one to five carbon atoms, more preferably from one to four carbon atoms, even more preferably from one to three carbon atoms, most preferably from one to two carbon atoms.
  • the R substituents hereof can also contain amino functionalities, e.g.
  • alkamino groups which can be primary, secondary or tertiary amines or quaternary ammonium. These include mono-, di- and tri- alkylamino and alkoxyamino groups wherein the aliphatic portion chain length is preferably as described above.
  • the R substituents can also be substituted with other groups, such as halogens (e.g. chloride, fluoride, and bromide), halogenated aliphatic or aryl groups, and hydroxy (e.g. hydroxy substituted aliphatic groups).
  • Suitable halogenated R groups could include, for example, tri- halogenated (preferably fluoro) alkyl groups such as -Rl-C(F)3, wherein R1 is
  • polysiloxanes examples include polymethyl -3,3,3 trifluoropropylsiloxane.
  • Suitable R groups include methyl, ethyl, propyl, phenyl, methylphenyl and phenylmethyl.
  • the preferred silicones are polydimethyl siloxane, polydiethylsiloxane, and polymethylphenylsiloxane. Polydimethylsiloxane is especially preferred.
  • Other suitable R groups include methyl, methoxy, ethoxy, propoxy, and aryloxy.
  • the three R groups on the end caps of the silicone may also represent the same or different groups.
  • nonvolatile polyalkylsiloxane fluids that may be used include, for example, polydimethylsiloxanes. These siloxanes are available, for example, from the General Electric Company in their Viscasil R and SF 96 series, and from Dow Corning in their Dow Corning 200 series.
  • polyalkylaryl siloxane fluids that may be used, also include, for example, polymethylphenylsiloxanes. These siloxanes are available, for example, from the General Electric Company as SF 1075 methyl phenyl fluid or from Dow Corning as 556 Cosmetic Grade Fluid.
  • the polyether siloxane copolymers that may be used include, for example, a polypropylene oxide modified polydimethylsiloxane (e.g., Dow Corning DC-1248) although ethylene oxide or mixtures of ethylene oxide and propylene oxide may also be used.
  • a polypropylene oxide modified polydimethylsiloxane e.g., Dow Corning DC-1248
  • ethylene oxide or mixtures of ethylene oxide and propylene oxide may also be used.
  • insoluble silicones the ethylene oxide and polypropylene oxide level must be sufficiently low to prevent solubility in water and the composition hereof.
  • Other suitable silicone fluids for use in the silicone conditioning agents are insoluble silicone gums. These gums are polyorganosiloxane materials having a viscosity at 25°C of greater than or equal to 1 ,000,000 centistokes. Silicone gums are described in U.S. Patent 4,152,416; Noll and Walter, Chemistry and Technology of Silicones.
  • the silicone gums will typically have a mass molecular weight in excess of about 200,000, generally between about 200,000 and about 1 ,000,000, specific examples of which include polydimethylsiloxane, (polydimethylsiloxane) (methylvinylsiloxane) copolymer, poly(dimethylsiloxane) (diphenyl siloxane)(methylvinylsiloxane) copolymer and mixtures thereof.
  • the silicone conditioning agent can also comprise a mixture of polydimethylsiloxane gum (viscosity greater than about 1 ,000,000 centistokes) and polydimethylsiloxane oil (viscosity from about 10 to about 100,000 centistokes), wherein the ratio of gum to fluid is from about 30:70 to about 70:30, preferably from about 40:60 to about 60:40.
  • the number average particle size of the optional silicone component can vary widely without limitation and will depend on the formulation and/or the desired characteristics. Number average particle sizes preferred for use in the present invention will typically range from about 10 nanometres to about 100 microns, more preferably from about 30 nanometres to about 20 microns.
  • compositions of the present invention can also comprise one or more cationic polymer conditioning agents.
  • the cationic polymer conditioning agents will preferably be water soluble.
  • Cationic polymers are typically at concentrations of from about 0.001% to about 20%, more typically from about 0.005% to about 10%, preferably from about 0.01% to about 2%, by weight, of the total composition.
  • water soluble cationic polymer By “water soluble” cationic polymer, what is meant is a polymer which is sufficiently soluble in water to form a substantially clear solution to the naked eye at a concentration of 0.1% in water (distilled or equivalent) at 25°C. Preferably, the polymer will be sufficiently soluble to form a substantially clear solution at 0.5% concentration, more preferably at 1.0% concentration.
  • polymer shall include materials whether made by polymerization of one type of monomer or made by two (i.e., copolymers) or more types of monomers.
  • the cationic polymers hereof will generally have a weight average molecular weight which is at least about 5,000, typically at least about 10,000, and is less than about 10 million. Preferably, the molecular weight is from about 100,000 to about 2 million.
  • the cationic polymers will generally have cationic nitrogen-containing moieties such as quaternary ammonium or cationic amino moieties, and mixtures thereof.
  • the cationic charge density is preferably at least about 0.1 meq/g, more preferably at least about 0.5 meq/g, even more preferably at least about 1.1 meq/g, most preferably at least about 1.2 meq/g.
  • the cationic polymers will have a cationic charge density of less than about 7meq/g, preferably less than about 5meq/g, more preferably less than about 3.5meq/g, even more preferably less than about 2.5meq/g.
  • Cationic charge density of the cationic polymer can be determined using the Kjeldahl Method (United States Pharmacopoeia - Chemical tests - ⁇ 461> Nitrogen Determination - method II). Those skilled in the art will recognise that the charge density of some amino-containing polymers may vary depending upon pH and the isoelectric point of the amino groups. The charge density should be within the above limits at the pH of intended use.
  • Any anionic counterions can be utilized for the cationic polymers so long as the water solubility criteria is met.
  • Suitable counterions include halides (e.g., Cl, Br, I, or F, preferably Cl, Br, or I), sulfate, and methylsulfate. Others can also be used, as this list is not exclusive.
  • the cationic nitrogen-containing moiety will be present generally as a substituent, on a fraction of the total monomer units of the cationic hair conditioning polymers.
  • the cationic polymer can comprise copolymers, terpolymers, etc. of quaternary ammonium or cationic amine-substituted monomer units and other non-cationic units referred to herein as spacer monomer units.
  • Such polymers are known in the art, and a variety can be found in the CTFA International Cosmetic Ingredient Dictionary and Handbook. 7th edition, edited by Wenninger and McEwen, (The Cosmetic, Toiletry, and Fragrance Association, Inc., Washington, D.C., 1997).
  • Suitable cationic polymers include, for example, copolymers of vinyl monomers having cationic amine or quaternary ammonium functionalities with water soluble spacer monomers such as acrylamide, methacrylamide, alkyl and dialkyl acrylamides, alkyl and dialkyl methacrylamides, alkyl acrylate, alkyl methacrylate, vinyl caprolactone, and vinyl pyrrolidone.
  • the alkyl and dialkyl substituted monomers preferably have C1-C7 alkyl groups, more preferably C1-C3 alkyl groups.
  • spacer monomers include vinyl esters, vinyl alcohol (made by hydrolysis of polyvinyl acetate), maleic anhydride, propylene glycol, and ethylene glycol.
  • the cationic amines can be primary, secondary, or tertiary amines, depending upon the particular species and the pH of the composition. In general, secondary and tertiary amines, especially tertiary amines, are preferred.
  • Amine-substituted vinyl monomers can be polymerised in the amine form, and then optionally can be converted to ammonium by a quatemization reaction.
  • Amines can also be similarly quaternized subsequent to formation of the polymer.
  • tertiary amine functionalities can be quaternized by reaction with a salt of the formula R'X wherein R' is a short chain alkyl, preferably a C1-C7 alkyl, more preferably a C1-C3 alkyl, and X is an anion which forms a water soluble salt with the quaternized ammonium.
  • Suitable cationic amino and quaternary ammonium monomers include, for example, vinyl compounds substituted with dialkylaminoalkyl acrylate, dialkylaminoalkyl methacrylate, monoalkylaminoalkyl acrylate, monoalkylaminoalkyl methacrylate, trialkyl methacryloxyalkyl ammonium salt, trialkyl acryloxyalkyl ammonium salt, diallyl quaternary ammonium salts, and vinyl quaternary ammonium monomers having cyclic cationic nitrogen-containing rings such as pyridinium, imidazolium, and quaternized pyrrolidone, e.g., alkyl vinyl imidazolium, alkyl vinyl pyridinium, alkyl vinyl pyrrolidone salts.
  • the alkyl portions of these monomers are preferably lower alkyls such as the C1-C3 alkyls, more preferably C 1 and C ⁇ alkyls.
  • Suitable amine-substituted vinyl monomers for use herein include dialkylaminoalkyl acrylate, dialkylaminoalkyl methacrylate, dialkylaminoalkyl acrylamide, and dialkylaminoalkyl methacrylamide, wherein the alkyl groups are preferably C1-C7 hydrocarbyls, more preferably C1-C3, alkyls.
  • the cationic polymers hereof can comprise mixtures of monomer units derived from amine- and/or quaternary ammonium-substituted monomer and/or compatible spacer monomers.
  • Suitable cationic hair conditioning polymers include, for example: copolymers of 1-vinyl-2-pyrrolidone and 1-vinyl-3-methylimidazolium salt (e.g., chloride salt) (referred to in the industry by the Cosmetic, Toiletry, and Fragrance Association, "CTFA", as Polyquaternium-16), such as those commercially available from BASF Wyandotte Corp.
  • Preferred cationic polymers for use herein are cationic polymers and copolymers of saccharides.
  • the cationic polysaccharides useful in the present invention include those polymers based on 5 or 6 carbon sugars and derivatives which have been made water-soluble by, for example, derivatising them with ethylene oxide. These polymers may be bonded via any of several arrangements, such as 1 ,4- ⁇ , 1 ,4- ⁇ , 1 ,3- , 1 ,3- ⁇ and 1 ,6 linkages.
  • the monomers may be in straight chain or branched chain geometric arrangements.
  • Suitable non-limiting examples of cationic polysaccharides include those based on the following: celluloses, hydroxyalkylcelluloses, starches, hydroxyalkylstarches, polymers based on arabinose monomers, polymers derived from xylose, polymers derived from fucose, polymers derived from fructose, polymers based on acid-containing sugars such as galacturonic acid and glucuronic acid, polymers based on amine sugars such as galactosamine and glucosamine particularly acetylglucosamine, polymers based on 5 or 6 membered ring polyalcohols, polymers based on galactose, polymers based on mannose monomers and polymers based on galactomannan copolymer known as guar gum.
  • cationic polymers based on celluloses and acetylglucosamine derivatives especially cationic polymers of cellulose derivatives.
  • suitable cationic polymers are those available from Amerchol Corp. (Edison, NJ, USA) as salts of hydroxyethyl cellulose reacted with trimethyl ammonium substituted epoxide, referred to in the industry (CTFA) as Polyquaternium 10. Background material on these polymers and their manufacture, can be found in U.S. Pat. No. 3,472,840 (issued Oct. 14 1969 to Stone), herein incorporated by reference.
  • cationic cellulose examples include the polymeric quaternary ammonium salts of hydroxyethyl cellulose reacted with lauryl dimethyl ammonium-substituted epoxide, referred to in the industry (CTFA) as Polyquaternium 24, available from Amerchol Corp. (Edison, NJ, USA) and polymeric quaternary ammonium salts of hydroxyethyl cellulose reacted with diallyl dimethyl ammonium chloride, referred to in the industry (CTFA) as Polyquaternium 4, available from National Starch (Salisbury, NC, USA).
  • CTFA polymeric quaternary ammonium salts of hydroxyethyl cellulose reacted with lauryl dimethyl ammonium-substituted epoxide
  • CTFA polyquaternium 24
  • Polyquaternium 4 available from National Starch (Salisbury, NC, USA).
  • the cationic copolymers of saccharides useful in the present invention encompass those containing the following saccharide monomers: glucose, galactose, mannose, arabinose, xylose, fucose, fructose, glucosamine, galactosamine, glucuronic acid, galacturonic acid, and 5 or 6 membered ring polyalcohols. Also included are hydroxy methyl, hydroxyethyl and hydroxypropyl derivatives of the above sugars.
  • saccharides When saccharides are bonded to each other in the copolymers, they may be bonded via any of several arrangements, such as 1 ,4- ⁇ , 1 ,4- ⁇ , 1 ,3- ⁇ , 1 ,3- ⁇ and 1 ,6 linkages.
  • Any other monomers can be used as long as the resultant polymer is suitable for use in hair care.
  • Non-limiting examples of other monomers useful herein include dimethyldiallylammonium chloride, dimethylaminoethylmethyl acrylate, diethyldiallylammonium chloride, N,N-diallyl,N-N-dialkyl ammonium halides, and the like.
  • the cationic polymer hereof is water soluble. This does not mean, however, that it must be soluble in the composition.
  • the cationic polymer is either soluble in the composition, or in a complex coacervate phase in the composition formed by the cationic polymer and anionic material.
  • Complex coacervates of the cationic polymer can be formed with anionic surfactants or with anionic polymers that can optionally be added to the compositions hereof (e.g., sodium polystyrene sulfonate).
  • the hair care compositions of the present invention may also comprise a sensate.
  • sensate means a substance that, when applied to the skin, causes a perceived sensation of a change in conditions, for example, but not limited to, heating, cooling, refreshing and the like.
  • Sensates are preferably utilized at levels of from about 0.001% to about 10%, more preferably from about 0.005% to about 5%, even more preferably from about 0.01 % to about 1 %, by weight, of the total composition.
  • sensate suitable for use in hair care compositions may be used herein.
  • a non-limiting, exemplary list of suitable sensates can be found in GB-B-1315626, GB-B-1404596 and GB-B-1411785, all incorporated by reference herein.
  • Preferred sensates for use in the compositions herein are camphor, menthol, I- isopulegol, ethyl menthane carboxamide and trimethyl isopropyl butanamide.
  • compositions of the present invention may optionally comprise C ⁇ Ce, preferably C 2 -C 3 , more preferably C 2 , aliphatic alcohol.
  • the aliphatic alcohol will generally comprise from about 1 % to about 75%, preferably from about 10% to about 40%, more preferably from about 15% to about 30%, even more preferably from about 18% to about 26%, by weight, of the total composition.
  • Suitable polyethylene glycol derivatives of glycerides include any polyethylene glycol derivative of glycerides which are water-soluble and which are suitable for use in a hair care composition.
  • Suitable polyethylene glycol derivatives of glycerides for use herein include derivatives of mono-, di- and tri-glycerides and mixtures thereof.
  • polyethylene glycol derivatives of glycerides suitable herein are those which conform to the general formula (I):
  • n the degree of ethoxylation, is from about 4 to about 200, preferably from about 5 to about 150, more preferably from about 20 to about 120, and wherein R comprises an aliphatic radical having from about 5 to about 25 carbon atoms, preferably from about 7 to about 20 carbon atoms.
  • Suitable polyethylene glycol derivatives of glycerides can be polyethylene glycol derivatives of hydrogenated castor oil.
  • PEG-20 hydrogenated castor oil PEG-30 hydrogenated castor oil, PEG-40 hydrogenated castor oil, PEG-45 hydrogenated castor oil, PEG-50 hydrogenated castor oil, PEG-54 hydrogenated castor oil, PEG-55 hydrogenated castor oil, PEG-60 hydrogenated castor oil, PEG-80 hydrogenated castor oil, and PEG-100 hydrogenated castor oil.
  • Preferred for use in the compositions herein is PEG-60 hydrogenated castor oil.
  • polyethylene glycol derivatives of glycerides can be polyethylene glycol derivatives of stearic acid.
  • PEG-30 stearate, PEG-40 stearate, PEG-50 stearate, PEG-75 stearate, PEG-90 stearate, PEG-100 stearate, PEG-120 stearate, and PEG-150 stearate PEG-100 stearate.
  • Cationic surfactants useful in compositions of the present invention contain amino or quaternary ammonium moieties.
  • the cationic surfactant will preferably, though not necessarily, be insoluble in the compositions hereof.
  • Cationic surfactants among those useful herein are disclosed in the following documents, all incorporated by reference herein: M.C. Publishing Co., McCutcheon's, Detergents & Emulsifiers. (North American edition 1979); Schwartz, et al.; Surface Active Agents. Their Chemistry and Technology. New York: Interscience Publishers, 1949; U.S. Patent 3,155,591 , Spotifyr, issued November 3, 1964; U. S. Patent 3,929,678, Laughlin et al., issued December 30, 1975; U.
  • R1-R4 are independently an aliphatic group of from about 1 to about 22 carbon atoms or an aromatic, alkoxy, polyoxyalkylene, alkylamido, hydroxyalkyl, aryl or alkylaryl group having from about 1 to about 22 carbon atoms; and X is a salt-forming anion such as those selected from halogen, (e.g. chloride, bromide), acetate, citrate, lactate, glycolate, phosphate nitrate, sulfate, and alkylsulfate radicals.
  • the aliphatic groups may contain, in addition to carbon and hydrogen atoms, ether linkages, and other groups such as amino groups.
  • the longer chain aliphatic groups e.g., those of about 12 carbons, or higher, can be saturated or unsaturated.
  • mono-long chain e.g., mono C12-C22. preferably C ⁇
  • di-short chain e.g., C1-C3 alkyl, preferably C1-C2 alkyl
  • Salts of primary, secondary and tertiary fatty amines are also suitable cationic surfactant materials.
  • the alkyl groups of such amines preferably have from about 12 to about 22 carbon atoms, and may be substituted or unsubstituted.
  • Such amines useful herein, include stearamido propyl dimethyl amine, diethyl amino ethyl stearamide, dimethyl stearamine, dimethyl soyamine, soyamine, myristyl amine, tridecyl amine, ethyl stearylamine, N-tallowpropane diamine, ethoxylated (with 5 moles of ethylene oxide) stearylamine, dihydroxy ethyl stearylamine, and arachidylbehenylamine.
  • Suitable amine salts include the halogen, acetate, phosphate, nitrate, citrate, lactate, and alkyl sulfate salts.
  • Such salts include stearylamine hydrochloride, soyamine chloride, stearylamine formate, N-tallowpropane diamine dichloride, stearamidopropyl dimethylamine citrate, cetyl trimethyl ammonium chloride and dicetyl diammonium chloride.
  • Preferred for use in the compositions herein is cetyl trimethyl ammonium chloride.
  • Cationic amine surfactants included among those useful in the present invention are disclosed in U.S. Patent 4,275,055, Nachtigal, et al., issued June 23, 1981 , incorporated by reference herein.
  • Cationic surfactants are preferably utilized at levels of from about 0.1% to about 10%, more preferably from about 0.25% to about 5%, most preferably from about 0.3% to about 0.7%, by weight of the composition.
  • the hair care compositions of the present invention may also comprise fatty alcohols. Any fatty alcohol suitable for use in hair care may be used herein. However, preferred are C 8 to C 22 , more preferred are C 12 to C 18 , even more preferred are C 16 , fatty alcohols.
  • Fatty alcohols are preferably utilized at levels of from about 0.1% to about 20%, more preferably from about 0.25% to about 10%, most preferably from about 0.5% to about 5%, by weight of the composition.
  • the ratio of alcohol:surfactant is preferably in the range of from about 3:1 to about 6:1 , more preferably 4:1.
  • compositions of the present invention will also generally contain water.
  • present water will generally comprise from about 25% to about 99%, preferably from about 50% to about 98%, more preferably from about 65% to about 95%, by weight, of the total composition. Additional Components
  • compositions herein can contain a variety of other optional components suitable for rendering such compositions more cosmetically or aesthetically acceptable or to provide them with additional usage benefits.
  • Such conventional optional ingredients are well-known to those skilled in the art.
  • additional ingredients can be formulated into the present composition. These include: other hair conditioning ingredients such as panthenol, panthetine, pantotheine, panthenyl ethyl ether, and combinations thereof; other solvents such as hexylene glycol; hair-hold polymers such as those described in WO-A-94/08557, herein incorporated by reference; detersive surfactants such as anionic, nonionic, amphoteric, and zwitterionic surfactants; additional viscosity modifiers and suspending agents such as xanthan gum, guar gum, hydroxyethyl cellulose, triethanolamine, methyl cellulose, starch and starch derivatives; viscosity modifiers such as methanolamides of long chain fatty acids such as cocomonoethanol amide; crystalline suspending agents; pearlescent aids such as ethylene glycol distearate; opacifiers such as polystyrene; preservatives such as phenoxyethanol, benzyl
  • compositions of the present invention can be formulated in a wide variety of product forms, including but not limited to creams, gels, aerosol or non- aerosol foams, mousses and sprays.
  • Mousses, foams and sprays can be formulated with propellants such as propane, butane, pentane, dimethylether, hydrofluorocarbon, C0 2 , N 2 0, or without specifically added propellants (using air as the propellant in a pump spray or pump foamer package).
  • propellants such as propane, butane, pentane, dimethylether, hydrofluorocarbon, C0 2 , N 2 0, or without specifically added propellants (using air as the propellant in a pump spray or pump foamer package).
  • the compositions of the present invention will be packaged in packages having instructions indicating that the composition is intended to be left on the hair.
  • the hair care compositions of the present invention may be used in a conventional manner for care of human hair.
  • An effective amount of the composition typically from about 1 gram to about 50 grams, preferably from about 1 gram to about 20 grams, is applied to the hair.
  • Application of the composition typically includes working the composition through the hair, generally with the hands and fingers, or with a suitable implement such as a comb or brush, to ensure good coverage.
  • the composition is then left on the hair, generally until the consumer next washes their hair.
  • the preferred method treating the hair therefore comprises the steps of:
  • the method can, optionally, comprise a further step of rinsing the hair with water.
  • ingredients A are added to water and stirred thoroughly under ambient conditions until a homogenous solution is obtained. All of ingredients B are mixed together and then added to the homogenous solution of ingredients A. All of ingredients C are then added and the resulting solution is thoroughly mixed.
  • All ingredients of A are solublised in water and then heated to 80°C. All of ingredients B are then added. The solution is then cooled to 30°C through a plate heat exchanger with simultaneous high shear mixing. The cooling rate is maintained at between 1.0 and 1.5°C/min. Approximately 50% of ingredient D, triethanolamine, is then added and the solution is mixed until homologous. All of ingredients C are then added and the resulting solution is high shear mixed until homogenous particle size distribution is achieved. Recirculation is then stopped to prevent shear stress damage to the product during completion of neutralisation. The remaining ingredient D is added until the specified pH and viscosity are reached.

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)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Cosmetics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Cette invention concerne une composition pour le soin des cheveux que l'on applique telle quelle, et qui comprend les éléments suivants: une résine à base de polysiloxane dont au moins un groupe substituant comprend des électrons délocalisés; et un modificateur de viscosité. Ces compositions sont faciles à étaler sur les cheveux et offrent de bonnes caractéristiques de conditionnement et de brillant tout en réduisant les sensations de gras et de collant.
PCT/US1998/015850 1998-07-30 1998-07-30 Compositions pour le soin des cheveux WO2000006095A1 (fr)

Priority Applications (9)

Application Number Priority Date Filing Date Title
PCT/US1998/015850 WO2000006095A1 (fr) 1998-07-30 1998-07-30 Compositions pour le soin des cheveux
AU87615/98A AU8761598A (en) 1998-07-30 1998-07-30 Hair care compositions
CN 99809931 CN1313747A (zh) 1998-07-30 1999-03-26 头发护理组合物
BR9912544-7A BR9912544A (pt) 1998-07-30 1999-03-26 Composição de tratamento de cabelo e processo de condicionamento de cabelo
PCT/US1999/006116 WO2000006104A1 (fr) 1998-07-30 1999-03-26 Compositions de soins capillaires
AU33592/99A AU3359299A (en) 1998-07-30 1999-03-26 Hair care compositions
EP99914963A EP1100439A1 (fr) 1998-07-30 1999-03-26 Compositions de soins capillaires
JP2000561961A JP2003521450A (ja) 1998-07-30 1999-03-26 ヘアケア組成物
CA002336680A CA2336680A1 (fr) 1998-07-30 1999-03-26 Compositions de soins capillaires

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US1998/015850 WO2000006095A1 (fr) 1998-07-30 1998-07-30 Compositions pour le soin des cheveux

Publications (1)

Publication Number Publication Date
WO2000006095A1 true WO2000006095A1 (fr) 2000-02-10

Family

ID=22267591

Family Applications (2)

Application Number Title Priority Date Filing Date
PCT/US1998/015850 WO2000006095A1 (fr) 1998-07-30 1998-07-30 Compositions pour le soin des cheveux
PCT/US1999/006116 WO2000006104A1 (fr) 1998-07-30 1999-03-26 Compositions de soins capillaires

Family Applications After (1)

Application Number Title Priority Date Filing Date
PCT/US1999/006116 WO2000006104A1 (fr) 1998-07-30 1999-03-26 Compositions de soins capillaires

Country Status (7)

Country Link
EP (1) EP1100439A1 (fr)
JP (1) JP2003521450A (fr)
CN (1) CN1313747A (fr)
AU (2) AU8761598A (fr)
BR (1) BR9912544A (fr)
CA (1) CA2336680A1 (fr)
WO (2) WO2000006095A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102014214463A1 (de) * 2014-07-24 2016-01-28 Beiersdorf Ag Deodorantzubereitungen umfassend Polyquaternium Polymere

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0095238A2 (fr) * 1982-05-20 1983-11-30 Dow Corning Corporation Compositions utiles pour le conditionnement des cheveux
EP0463780A2 (fr) * 1990-06-20 1992-01-02 Unilever N.V. Composition sous forme de shampooing
FR2676923A1 (fr) * 1991-06-03 1992-12-04 Oreal Composition de traitement des matieres keratiniques a base de silicone et de latex.
WO1994008557A1 (fr) * 1992-10-22 1994-04-28 The Procter & Gamble Company Compositions pour soins favorisant la coiffure et le brillant

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0095238A2 (fr) * 1982-05-20 1983-11-30 Dow Corning Corporation Compositions utiles pour le conditionnement des cheveux
EP0463780A2 (fr) * 1990-06-20 1992-01-02 Unilever N.V. Composition sous forme de shampooing
FR2676923A1 (fr) * 1991-06-03 1992-12-04 Oreal Composition de traitement des matieres keratiniques a base de silicone et de latex.
WO1994008557A1 (fr) * 1992-10-22 1994-04-28 The Procter & Gamble Company Compositions pour soins favorisant la coiffure et le brillant

Also Published As

Publication number Publication date
AU8761598A (en) 2000-02-21
AU3359299A (en) 2000-02-21
WO2000006104A1 (fr) 2000-02-10
BR9912544A (pt) 2001-05-02
JP2003521450A (ja) 2003-07-15
EP1100439A1 (fr) 2001-05-23
CA2336680A1 (fr) 2000-02-10
CN1313747A (zh) 2001-09-19

Similar Documents

Publication Publication Date Title
US6589517B1 (en) Hair care compositions
US5997851A (en) Hair care compositions containing low melting point fatty alcohol and ethylene oxide/propylene oxide polymer
MX2008001940A (es) Uso de espesantes polimericos en composiciones para el tratamiento del cabello, metodo y composicion.
US6627183B1 (en) Hair care compositions
WO1995009600A1 (fr) Compositions de soins capillaires contenant des alcools gras a bas point de fusion et des epaississants polymeres reticules
CA2337165C (fr) Compositions de soins capillaires
EP1100440B1 (fr) Compositions de soins capillaires contenant des resines de polysiloxane substituées par du 2-phenylpropyl
WO2000006096A1 (fr) Compositions pour le conditionnement des cheveux
WO2000006101A1 (fr) Compositions pour le soin des cheveux
WO2000006095A1 (fr) Compositions pour le soin des cheveux
WO2001070180A1 (fr) Compositions de traitement capillaire antipelliculaire
WO2001022929A1 (fr) Compositions pour les soins des cheveux
MXPA01001085A (en) Hair care compositions comprising polysiloxane resins with delocalised electrons
MXPA01001130A (en) Hair care compositions
MXPA01001080A (es) Composiciones para el cuidado del cabello
MXPA01001084A (en) Hair care compositions
MXPA01001129A (en) Hair care compositions
WO2001022927A1 (fr) Compositions pour l'entretien des cheveux

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AL AM AT AU AZ BA BB BG BR BY CA CH CN CU CZ DE DK EE ES FI GB GE GH GM HR HU ID IL IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT UA UG US UZ VN YU ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW SD SZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

NENP Non-entry into the national phase

Ref country code: CA