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DE19820949A1 - Hair spray composition with good application properties - Google Patents

Hair spray composition with good application properties

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Publication number
DE19820949A1
DE19820949A1 DE1998120949 DE19820949A DE19820949A1 DE 19820949 A1 DE19820949 A1 DE 19820949A1 DE 1998120949 DE1998120949 DE 1998120949 DE 19820949 A DE19820949 A DE 19820949A DE 19820949 A1 DE19820949 A1 DE 19820949A1
Authority
DE
Germany
Prior art keywords
weight
hair spray
spray composition
good application
application properties
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
DE1998120949
Other languages
German (de)
Inventor
Wilma M Dausch
Volker Schehlmann
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
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 BASF SE filed Critical BASF SE
Priority to DE1998120949 priority Critical patent/DE19820949A1/en
Publication of DE19820949A1 publication Critical patent/DE19820949A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/06Preparations for styling the hair, e.g. by temporary shaping or colouring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/046Aerosols; Foams
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions 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
    • A61K8/8152Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions 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
    • A61K8/8158Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817Compositions 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)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/88Polyamides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A61K8/894Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical 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)
  • Dispersion Chemistry (AREA)
  • Cosmetics (AREA)

Abstract

Hair spray composition contains 0.1-15 wt.% fixing polymer, 0.01-0.5 wt.% siloxane(s) selected from hexamethyldisiloxane, dimethicone copolyol and laurylmethicone copolyol, 0-10 wt.% usual additives, propellant, organic solvent and optionally water.

Description

Für die Festigung von Haarfrisuren werden seit fast 50 Jahren erfolgreich synthetische Polymere eingesetzt. Während in der An­ fangszeit bevorzugt Vinyllactam-Homo- und Copolymere zum Einsatz gelangten, haben später carboxylatgruppenhaltige Polymere zu­ nehmend an Bedeutung gewonnen. Das gewünschte Eigenschaftsprofil wie starke Festigung bei hoher Luftfeuchtigkeit, Elastizität, Auswaschbarkeit vom Haar und Verträglichkeit mit den übrigen Formulierungskomponenten werden durch Copolymerisation einer Kombination von hydrophoben, elastifizierenden und carboxyl­ gruppen enthaltenden Monomeren erzielt (Lit.: Robert Y. Lochhead, Vol. 103, December 1988, 24 ff., Rolf-Dieter Reinhardt Cosmetics and Toiletries Manufacture World Wide 1995, 189m ff.).For setting hairstyles have been used for almost 50 years successfully used synthetic polymers. While in the An In the beginning, vinyl lactam homo- and copolymers are preferred later have polymers containing carboxylate groups gaining in importance. The desired property profile like strong consolidation with high air humidity, elasticity, Washable from the hair and compatibility with the rest Formulation components are obtained by copolymerization of a Combination of hydrophobic, elasticizing and carboxyl group-containing monomers (Lit .: Robert Y. Lochhead, Vol. 103, December 1988, 24 ff., Rolf-Dieter Reinhardt Cosmetics and Toiletries Manufacture World Wide 1995, 189m ff.).

Während die obengenannten Anforderungen heute von verschiedenen Polymertypen erreicht werden, wird immer häufiger der Griff der mit diesen Polymeren gefestigten Frisuren als unangenehm stumpf und "unnatürlich" empfunden. Versuche durch Zusätze zu den Formu­ lierungen zu einer Verbesserung zu gelangen, führten bisher nicht zu voll befriedigenden Ergebnissen: Die Zugabe üblicher Weich­ macher verbessert zwar den Griff, reduziert aber gleichzeitig in vielen Fällen die Festigungswirkung.While the above requirements are different today Polymer types are achieved, the grip of the hairstyles consolidated with these polymers as uncomfortably dull and felt "unnatural". Try adding to the formu There have so far been no improvements to fully satisfactory results: the addition of conventional soft machinist improves the grip, but at the same time reduces in the strengthening effect in many cases.

In US 5,599,524 werden Haarsprayzusammensetzungen beschrieben, die neben dem festigenden Polymer und üblichen Zusatzstoffen bestimmte Siloxane (Hexamethyldisiloxan, Bisphenylhexamethicone) in einer Menge von 0.6 bis 5 Gew.-% enthalten. Diese Haarspray­ zusammensetzungen weisen eine verbesserte Sprühcharakteristik auf, während andere Siloxane wie beispielsweise Dimethicone zu keiner verbesserten Sprühcharakteristik beitragen (Beispiel 1). Bei einer Polymermenge von 5 Gew.-% und einer Siloxanmenge von 1 Gew.-% besitzen diese Haarsprayzusammensetzungen bezüglich Glanz, Steifheit, Trockenkämmbarkeit und Flaking keine Vorteile gegen­ über den Siloxan-freien Haarsprayzusammensetzungen (Beispiel 3).No. 5,599,524 describes hairspray compositions which in addition to the setting polymer and usual additives certain siloxanes (hexamethyldisiloxane, bisphenylhexamethicone) contained in an amount of 0.6 to 5 wt .-%. This hairspray compositions have improved spray characteristics while other siloxanes such as dimethicone do not contribute to improved spray characteristics (example 1). With a polymer amount of 5% by weight and a siloxane amount of 1 % By weight have these hairspray compositions in terms of gloss, Rigidity, combability and flaking have no advantages over the siloxane-free hair spray compositions (Example 3).

Überraschenderweise wurde jetzt gefunden, daß Haarsprayzusammen­ setzungen mit einem genau definierten relativ niedrigen Gehalt an spezifischen Siloxanen besonders vorteilhafte anwendungs­ technische Eigenschaften besitzen. Surprisingly, it has now been found that hairspray together settlements with a precisely defined, relatively low salary with specific siloxanes particularly advantageous application possess technical characteristics.  

Die Erfindung betrifft Haarsprayzusammensetzung enthaltend
The invention relates to hairspray composition containing

  • A) 0,1 bis 15 Gew.-% festigende Polymere,A) 0.1 to 15% by weight of setting polymers,
  • B) 0,01 bis 0,5 Gew.-% eines oder mehrerer Siloxane aus der Gruppe Hexamethyldisiloxan, Dimethicone Copolyol und Lauryl­ methicone Copolyol ist,B) 0.01 to 0.5 wt .-% of one or more siloxanes from the Group hexamethyldisiloxane, dimethicone copolyol and lauryl methicone copolyol is
  • C) 0 bis 10 Gew.-% üblicher Zusatzstoffe,C) 0 to 10% by weight of conventional additives,
  • D) Treibmittel,D) blowing agent,
  • E) organische Lösungsmittel und ggf. Wasser,
    wobei die Komponenten (A) bis (E) zusammen 100 Gew.-% betragen.
    E) organic solvents and possibly water,
    the components (A) to (E) together being 100% by weight.

Geeignete festigende Polymere (A) sind seit langem dem Fachmann bekannt, insbesondere solche aus Copolymere aus Vinylacetat/- Crotonsäure/Vinylneodecanoat; Octylacrylamid/Acrylat/Butylamino­ ethyl Methacrylat; Vinylacetat/ Crotonat; Polyvinylpyrrolidon (PVP); Polyvinylpyrrolidon/Vinylacetat; PVP/Acrylat; Vinylacetat/- Crotonsäure/Vinylpropionat; Acrylat/Acrylamid; Acrylat/Octyl - acrylamid und Alkylester von Polyvinylmethylether/Maleinsäure­ anhydrid; Diglycol/Cyclohexandimethanol/Isophthalat/Sulfoiso­ phthalat; Vinylacetat/Butylmaleat/Isobornylacrylat; Vinyl­ caprolactam/PVP/Dimethylaminoethylmethacrylat; Vinylacetat/Alkyl - maleat-Halbester/N-substituierte Acrylamid Terpolymere; Vinyl­ caprolactam/Vinylpyrrolidon/Methacrylamidopropyltrimethyl­ ammoniumchlorid Terpolymer; Methacrylat/Acrylat Copolymer Amin­ salz; Methacrylsäure/Tert. Butylacrylat u. ggf. weitere Acryl­ ester.Suitable setting polymers (A) have long been known to the person skilled in the art known, especially those made from copolymers of vinyl acetate / - Crotonic acid / vinyl neodecanoate; Octylacrylamide / acrylate / butylamino ethyl methacrylate; Vinyl acetate / crotonate; Polyvinyl pyrrolidone (PVP); Polyvinyl pyrrolidone / vinyl acetate; PVP / acrylate; Vinyl acetate / - Crotonic acid / vinyl propionate; Acrylate / acrylamide; Acrylate / octyl - acrylamide and alkyl esters of polyvinyl methyl ether / maleic acid anhydride; Diglycol / cyclohexanedimethanol / isophthalate / sulfoiso phthalate; Vinyl acetate / butyl maleate / isobornyl acrylate; Vinyl caprolactam / PVP / dimethylaminoethyl methacrylate; Vinyl acetate / alkyl - maleate half ester / N-substituted acrylamide terpolymers; Vinyl caprolactam / vinylpyrrolidone / methacrylamidopropyltrimethyl ammonium chloride terpolymer; Methacrylate / acrylate copolymer amine salt; Methacrylic acid / tert. Butyl acrylate u. possibly further acrylic ester.

Bei der Verwendung von carboxylatgruppenhaltigen Polymeren (A) werden die Carboxylatgruppen der Polymerisate, zweckmäßigerweise teilweise oder vollständig neutralisiert. Diese Neutralisierung kann bei der Herstellung der Polymeren oder bei Endformulierung der Haarsprayzusammensetzung erfolgen.When using carboxylate group-containing polymers (A) the carboxylate groups of the polymers, expediently partially or completely neutralized. This neutralization can be used in the preparation of the polymers or in the final formulation the hairspray composition.

Besonders geeignete Polymere (A) sind Vinylpyrrolidon Copolymere, wie sie beispielsweise unter dem Markennamen LUVISKOL® von der BASF Aktiengesellschaft vertrieben werden und Acrylatcopolymere wie sie beispielsweise unter dem Markennamen LUVIMER® und ULTRAHOLD® von der BASF Aktiengesellschaft vertrieben werden.Particularly suitable polymers (A) are vinyl pyrrolidone copolymers, as for example under the brand name LUVISKOL® from the BASF Aktiengesellschaft are distributed and acrylate copolymers as for example under the brand names LUVIMER® and ULTRAHOLD® are sold by BASF Aktiengesellschaft.

Die erfindungsgemäßen Haarfestigungsmittel enthalten die Polymere (A) in einer Menge von 0,5-15, bevorzugt von 2-10 Gew.-%. The hair fixatives according to the invention contain the polymers (A) in an amount of 0.5-15, preferably 2-10% by weight.  

Die Siloxane (B) sind bekannt und kommerziell erhältlich. Hexa­ methyldisiloxan wird beispielsweise von der Firma Rhone-Poulenc unter dem Markennamen MIRASIL HMS® verkauft.The siloxanes (B) are known and commercially available. Hexa methyldisiloxane is for example from the company Rhone-Poulenc sold under the brand name MIRASIL HMS®.

Dimethicone Copolyol wird beispielsweise von Dow Chemicals Inc. unter dem Markennamen DOW CORNING 190®, oder von Union Carbide unter den Markennamen SILWET COPOLYMER L-7500®, L-7087®, L-7602®, L-7622® oder SILSOFT 900® vertrieben.For example, Dimethicone Copolyol is available from Dow Chemicals Inc. under the brand name DOW CORNING 190®, or from Union Carbide under the brand names SILWET COPOLYMER L-7500®, L-7087®, L-7602®, L-7622® or SILSOFT 900® sold.

Laurylmethicone Copolyol wird beispielsweise von Dow Chemicals Inc. unter dem Markennamen DOW CORNING 5200® vertrieben.Laurylmethicone copolyol is available, for example, from Dow Chemicals Inc. sold under the brand name DOW CORNING 5200®.

Die Siloxane (B) werden in einer Menge von 0,01-0,5 Gew.-%, bevorzugt 0,03-0,25 Gew.-% eingesetzt. Die Mengenangabe bezieht sich auf die fertig formulierte Haarsprayzusammensetzung.The siloxanes (B) are used in an amount of 0.01-0.5% by weight, preferably 0.03-0.25 wt .-% used. The quantity refers the formulated hairspray composition.

Die Siloxane können sowohl als Einzelverbindungen als auch als Mischung verwendet werden.The siloxanes can be used both as individual compounds and as Mixture can be used.

Als Zusatzstoffe (C) können übliche Zusatzstoffe wie Lichtschutz­ mittel, Parfümöle, Farbstoffe, Antistatika, Konservierungsmittel, Verdicker in einer Menge bis zu 10 Gew.-% zugegeben werden.Additives (C) can be conventional additives such as light protection medium, perfume oils, dyes, antistatic agents, preservatives, Thickeners can be added in an amount of up to 10% by weight.

Als Treibmittel (D) können üblicherweise Kohlenwasserstoffe wie Propan, Butan, Isobutan oder Mischungen davon allein oder in Ver­ bindung mit komprimierten Gasen wie Stickstoff, Luft oder Kohlen­ dioxid verwendet werden. (D) wird üblicherweise in Mengen von 10 bis 60 Gew.-% eingesetzt.Hydrocarbons such as Propane, butane, isobutane or mixtures thereof alone or in ver binding with compressed gases such as nitrogen, air or coal dioxide can be used. (D) is usually used in amounts of 10 to 60 wt .-% used.

Als Komponente (E) können organische Lösungsmittel allein oder zusammen mit Wasser eingesetzt werden. Bevorzugt werden flüchtige Alkohole wie Methanol, Ethanol, Propanol, Isopropanol, Butanol, Ketone wie Aceton, Ether wie Dimethoxymethan und Dimethylether und Methylenchlorid, Bevorzugt werden als (E) Ethanol oder Ethanol/Wasser Gemische, insbesondere 80 : 20 verwendet.As component (E) organic solvents alone or can be used together with water. Volatile are preferred Alcohols such as methanol, ethanol, propanol, isopropanol, butanol, Ketones such as acetone, ethers such as dimethoxymethane and dimethyl ether and methylene chloride, Preferred as (E) ethanol or ethanol / water mixtures are in particular 80:20 used.

Die Komponente (E) wird üblicherweise in Mengen von 25 bis 90 Gew.-% eingesetzt.Component (E) is usually used in amounts of 25 to 90 wt .-% used.

BeispieleExamples

Im folgenden wurde eine Reihe von Haarsprayzusammensetzungen hergestellt und auf ihre anwendungstechnischen Eigenschaften überprüft. Der Übersichtlichkeit wegen sind die Ergebnisse in Tabelle 1 zusammengefaßt (Bewertung wie in der Schule). The following are a number of hair spray compositions manufactured and their application properties checked. For the sake of clarity, the results are in Table 1 summarized (evaluation as in school).  

Claims (3)

1. Haarsprayzusammensetzung enthaltend
  • A) 0,1 bis 15 Gew.-% festigende Polymere,
  • B) 0,01 bis 0,5 Gew.-% eines oder mehrerer Siloxane aus der Gruppe Hexamethyldisiloxan, Dimethicone Copolyol und Laurylmethicone Copolyol ist,
  • C) 0 bis 10 Gew.-% üblicher Zusatzstoffe,
  • D) Treibmittel,
  • E) organische Lösungsmittel und ggf. Wasser, wobei die Komponenten (A) bis (E) zusammen 100 Gew.-% betragen.
1. Containing hairspray composition
  • A) 0.1 to 15% by weight of setting polymers,
  • B) 0.01 to 0.5% by weight of one or more siloxanes from the group consisting of hexamethyldisiloxane, dimethicone copolyol and laurylmethicone copolyol,
  • C) 0 to 10% by weight of conventional additives,
  • D) blowing agent,
  • E) organic solvents and optionally water, the components (A) to (E) together being 100% by weight.
2. Haarsprayzusammensetzung nach Anspruch 1, wobei (B) Hexa­ methyldisiloxan ist.2. The hairspray composition of claim 1, wherein (B) hexa is methyldisiloxane. 3. Haarsprayzusammensetzung nach Anspruch 1, wobei (A) ein Acrylatcopolymer ist.The hairspray composition of claim 1, wherein (A) is a Is acrylate copolymer.
DE1998120949 1998-05-11 1998-05-11 Hair spray composition with good application properties Withdrawn DE19820949A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Application Number Priority Date Filing Date Title
DE1998120949 DE19820949A1 (en) 1998-05-11 1998-05-11 Hair spray composition with good application properties

Publications (1)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2858933A1 (en) * 2003-08-22 2005-02-25 Oreal Aerosol device contains a hair treatment composition comprising a silicone and a copolymer with a monomer composition gradient and dimethyl ether as propellant
WO2008012938A1 (en) * 2006-07-25 2008-01-31 Shiseido Company, Ltd. Aerosol type cosmetic hair preparations

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2858933A1 (en) * 2003-08-22 2005-02-25 Oreal Aerosol device contains a hair treatment composition comprising a silicone and a copolymer with a monomer composition gradient and dimethyl ether as propellant
WO2005020941A3 (en) * 2003-08-22 2005-06-09 Oreal Aerosol device containing a silicone, a graded copolymer and a propellant essentially comprising dimethylether
WO2008012938A1 (en) * 2006-07-25 2008-01-31 Shiseido Company, Ltd. Aerosol type cosmetic hair preparations
CN101472549B (en) * 2006-07-25 2012-03-21 株式会社资生堂 Aerosol type cosmetic hair preparations

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