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EP3057567A2 - Produits cosmétiques anti-transpirants aux alpha-hydroxyacides - Google Patents

Produits cosmétiques anti-transpirants aux alpha-hydroxyacides

Info

Publication number
EP3057567A2
EP3057567A2 EP14796688.1A EP14796688A EP3057567A2 EP 3057567 A2 EP3057567 A2 EP 3057567A2 EP 14796688 A EP14796688 A EP 14796688A EP 3057567 A2 EP3057567 A2 EP 3057567A2
Authority
EP
European Patent Office
Prior art keywords
aluminum
antiperspirant
cosmetic agent
weight
antiperspirant cosmetic
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Withdrawn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
EP14796688.1A
Other languages
German (de)
English (en)
Inventor
Bernhard Banowski
Christian Kropf
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.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
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 Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP3057567A2 publication Critical patent/EP3057567A2/fr
Withdrawn legal-status Critical Current

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
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/26—Aluminium; 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
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36—Carboxylic acids; Salts or anhydrides thereof
    • A61K8/365—Hydroxycarboxylic acids; Ketocarboxylic acids
    • 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
    • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
    • A61K8/498—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom having 6-membered rings or their condensed derivatives, e.g. coumarin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q15/00—Anti-perspirants or body deodorants
    • 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
    • A61K2800/52—Stabilizers

Definitions

  • the present invention relates to an antiperspirant cosmetic agent which contains at least one antiperspirant aluminum salt and at least one alpha-hydroxy acid and wherein the addition of the at least one alpha-hydroxy acid results in an effective activation of the at least one antiperspirant aluminum salt and in a stabilization of this activated state.
  • the present invention relates to the use of a combination of at least one antiperspirant aluminum salt and at least one alpha-hydroxy acid for reducing and / or preventing underarm perspiration.
  • the present invention relates to a non-therapeutic cosmetic method for preventing and / or reducing transpiration of the body, in which the antiperspirant according to the invention is applied to the skin, in particular to the skin of the armpits.
  • the present invention relates to the use of an alpha-hydroxy acid for the activation and / or stabilization of an antiperspirant aluminum salt.
  • washing, cleansing and caring for one's own body is a basic human need, and modern industry is constantly trying to meet these needs of man in a variety of ways. Especially important for daily hygiene is the permanent elimination or at least reduction of body odor and underarm wetness.
  • Numerous specific deodorant or antiperspirant personal care products are known in the art which have been developed for use in body regions having a high density of sweat glands, especially in the underarm area. These are formulated in a wide variety of dosage forms, for example as powder, in stick form, as aerosol spray, pump spray, liquid and gel roll on application, cream, gel and as impregnated flexible substrates (towels).
  • Prior art cosmetic antiperspirants contain at least one antiperspirant salt in addition to at least one oil or fatty substance and one perfume component or perfume.
  • basic aluminum and aluminum zirconium halides are used in the form of chlorides, as they have no irritating effect, unlike the non-basic aluminum and aluminum zirconium chlorides.
  • the disadvantage of the basic aluminum and aluminum zirconium halides is the formation of higher molecular weight oligomeric and polymeric aluminum species, which significantly reduce the effectiveness of the basic aluminum and aluminum zirconium salts in antiperspirants.
  • EP 0 308 937 A2, EP 0 183 171 A2, US Pat. No. 4,359,456 A and EP 0 191 628 A2 describe basic aluminum and aluminum zirconium halides, in particular aluminum chlorides, which have been obtained by a thermal treatment.
  • the heat-treated activated basic aluminum and aluminum zirconium halides have a lower content of high molecular weight species in gel permeation chromatography (GPC) compared to untreated basic aluminum and aluminum zirconium halides and thus enhanced antiperspirant efficacy against antiperspirants.
  • GPC gel permeation chromatography
  • a disadvantage of the aforementioned activated basic aluminum and aluminum zirconium halides of the prior art is the decrease in the antiperspirant effect with increasing storage time and / or when using protic solvents. This is due to the fact that the polymer distribution of the aluminum species is based on a reversible equilibrium and shifts this equilibrium in protic solvents with increasing time to higher molecular weight and thus less effective aluminum species.
  • antiperspirant cosmetic products which, even during long storage periods and / or when using high amounts of protic solvents, have no shift in the polymer distribution to long-chain polymers and thus no significant decrease in the antiperspirant effect. Furthermore, the antiperspirants should be inexpensive to produce.
  • the subject of the present invention is thus an antiperspirant cosmetic containing
  • R is a linear or branched alkyl group having 1 to 6 carbon atoms
  • R 2 , R 3 , R 4 and R 5 each independently represent hydrogen, -OH, a linear or branched alkyl group having 1 to 8 carbon atoms, an alkoxy group 1 to 6 carbon atoms, -NH 2, a galactopyranose residue or a galactopyranose residue partially or fully alkoxylated with ⁇ -6-alkyl groups
  • R 7 , R 8 , R 9 and R 0 each independently of one another, represent hydrogen, an alkoxy group having 1 to 6 carbon atoms or -OH,
  • y is a number from 0 to 5
  • X + for H + Li + , Na + , K + , NH 4 + , 7 2 Mg 2+ , 7 2 Ca 2+ , V 2 Mn 2+ , V 2 Zn 2+ , V 3 Al 3+ , V 4 Zr 4 "or at least one antiperspirant aluminum salt, and
  • Y + is Li + , Na + , V 2 Mg 2+ , V 2 Ca 2+ , V 2 Mn 2+ , V 2 Zn 2+ , V 3 Al 3+ , V 4 Zr 4 "or at least one antiperspirant aluminum salt .
  • X + is Li + , Na + , K + , NH 4 + , V 2 Mg 2+ , V 2 Ca 2+ , V 2 Mn 2+ , V 2 Zn 2+ , V 3 Al 3+ , 4 Zr 4 * or at least one antiperspirant aluminum salt is when R 4 is a Galactopyranoserest.
  • antiperspirant aluminum salts with special alpha hydroxy acids of the formulas (HS-I) and / or (HS-II) and / or (HS-III) is - without wishing to be limited to this theory - a significant increase in the proportion achieved on short-chain species of antiperspirant aluminum salts. Furthermore, the thus formed short-chain species are excellently stabilized by the aforementioned alpha-hydroxy acids, so that an improved antiperspirant effect is ensured over a long period of time.
  • the use of the special alpha-hydroxy acids makes it possible, in particular, to prepare antiperspirants with a high proportion of protic solvents which, despite the high amounts of protic solvents, have an excellent antiperspirant effect even during prolonged storage periods.
  • antiperspirant is understood according to the invention to reduce or reduce the perspiration of the sweat glands of the body.
  • cosmetic oil in the sense of the present invention is understood as meaning an oil which is suitable for cosmetic use and which is immiscible with water.Furthermore, the cosmetic oil used according to the invention is neither fragrance nor essential oils.
  • fragments in the context of the present invention means substances having a molecular weight of 74 to 300 g / mol, which contain at least one osmophoric group in the molecule and have an odor and / or taste, ie they are able to Osmophore groups are groups covalently bound to the molecular skeleton in the form of hydroxy groups, formyl groups, oxo groups, alkoxycarbonyl groups, nitrile groups, nitro groups, azide groups, etc.
  • fragments within the meaning of present invention even at 20 ° C and 1013 hPa liquid perfume oils, perfumes, or perfume oil ingredients.
  • the term "waxes" in the context of the present invention means substances which are kneadable at 20 ° C. or solid to brittle, have a coarse to fine-crystalline structure and are translucent to opaque, but not vitreous, in color Substances above 25 ° C without decomposition, slightly liquid above the melting point (slightly viscous), have a strong temperature-dependent consistency and solubility and are polishable under light pressure.
  • volatile cosmetic oil refers according to the invention cosmetic oils which at 20 ° C and an ambient pressure of 1013 hPa a vapor pressure of 2.66 Pa to 40,000 Pa (0.02 to 300 mm Hg), preferably from 10 to 12,000 Pa (0.1 to 90 mm Hg), more preferably from 13 to 3000 Pa (0.1 to 23 mm Hg), in particular from 15 to 500 Pa ( 0, 1 to 4 mm Hg).
  • nonvolatile cosmetic oils in the context of the present invention means cosmetic oils which have a vapor pressure of less than 2.66 Pa (0.02 mm Hg) at 20 ° C. and an ambient pressure of 1013 hPa.
  • fatty acid as used in the present invention means aliphatic carboxylic acids which have unbranched or branched carbon residues of 4 to 40 carbon atoms also be synthetically produced fatty acids.Furthermore, the fatty acids may be monounsaturated or polyunsaturated.
  • fatty alcohol in the context of the present invention means aliphatic, monohydric, primary alcohols which have unbranched or branched hydrocarbon radicals having 4 to 40 carbon atoms
  • the fatty alcohols used in the context of the invention may also be monounsaturated or polyunsaturated ,
  • wt .-% refers in the present case, unless otherwise stated, on the total weight of the antiperspirant cosmetic agents according to the invention without any optional propellant.
  • the cosmetic oil which is liquid at 20 ° C and 1 .013 hPa is selected from the group of
  • volatile cyclic silicone oils especially cyclotrisiloxane, cyclotetrasiloxane, cyclopentasiloxane and cyclohexasiloxane, and linear silicone oils having 2 to 10 siloxane units, especially hexamethyldisiloxane, octamethyltrisiloxane, decamethyltetrasiloxane;
  • volatile non-silicone oils especially liquid paraffin oils and isoparaffin oils such as isodecane, isoundecane, isododecane, isotridecane, isotetradecane, isopentadecane, isohexadecane and isoeicosan;
  • nonvolatile silicone oils especially higher molecular weight linear polyalkylsiloxanes
  • non-volatile non-silicone oils especially the esters of linear or branched saturated or unsaturated C 2 to C fatty acids having linear or branched saturated or unsaturated C 2 to C 30 fatty acids which may be hydroxylated, the C 8 to C 22 fatty alcohol esters more monohydric or polyhydric C 2 -C 7 -hydroxycarboxylic acids, the triethyl citrates, the branched saturated or unsaturated C 6 -C 30 -fatty alcohols, the mono-, di- and triglycerides of linear or branched, saturated or unsaturated, optionally hydroxylated C 3 -o-fatty acids, the dicarboxylic esters of linear or branched C 2 -C 10 alkanols, the Addition products of ethylene oxide and / or propylene oxide to mono- or polyhydric C3-22 alkanols, which may optionally be esterified, the symmetrical, asymmetrical or cyclic esters of carbon
  • the cyclic volatile silicone oils which can be used in the context of the invention have a vapor pressure of from 13 to 15 Pa (0.1 mm Hg) at 20 ° C. and an ambient pressure of 1013 hPa. Furthermore, according to the invention as a linear volatile silicone oil and a low molecular weight phenyl trimethicone having a vapor pressure of about 2,000 Pa (15 mm Hg) at 20 ° C and an ambient pressure of 1013 hPa can be used.
  • cyclic volatile silicone oils used in the antiperspirant cosmetic agents according to the invention become.
  • volatile non-silicone oils in the form of ⁇ -13-isoparaffine mixtures having a vapor pressure of from 10 to 400 Pa (0.08 to 3 mm Hg), preferably from 13 to 100 Pa (0.1 to 0.8 mm Hg). , used at 20 ° C and an ambient pressure of 1 .013 hPa.
  • volatile C 8 -C 16 isoparaffin it is preferred in the context of the present invention for the volatile C 8 -C 16 isoparaffin to be present in a total amount of from 1 to 60% by weight, preferably from 3 to 45% by weight, preferably from 5 to 40% by weight.
  • % in particular from 8 to 20 wt .-%, based on the total weight of the antiperspirant cosmetic agent is included.
  • antiperspirant cosmetic products with a low proportion of volatile oils - that is, with 0.5 to 15 wt .-%, based on the total weight of the antiperspirant cosmetic agent, on volatile oils - or even without volatile oils to formulate.
  • the antiperspirant cosmetic agents comprise a non-volatile silicone oil and / or a non-volatile non-silicone oil.
  • preferred antiperspirant cosmetic agents contain at least one ester of linear or branched saturated or unsaturated fatty alcohols having 2 to 30 carbon atoms with linear or branched saturated or unsaturated fatty acids having 2 to 30 carbon atoms, which may be hydroxylated, in a total amount of 1 to 30 wt .-%, preferably from 5 to 26 wt .-%, preferably from 9 to 24 wt .-%, in particular from 12 to 17 wt .-%, based on the total weight of the antiperspirant cosmetic agent.
  • non-volatile silicone oils may be linear polyalkylsiloxanes having a kinematic viscosity of from 5 to 2,000 cSt at 25 ° C., in particular linear polydimethylsiloxanes having a kinematic viscosity at 25 ° C. of from 5 to 2,000 cSt, preferably from 10 to 350 cSt, in particular from 50 to 100 cSt.
  • the non-volatile silicone oils mentioned above are available under the tradenames Dow Corning ® 200 or Xiameter PMX from Dow Corning or Xiameter.
  • nonvolatile silicone oils are phenyltrimethicones having a kinematic viscosity at 25 ° C. of from 10 to 100 cSt, preferably from 15 to 30 cSt, and also cetyldimethicones.
  • the cosmetic oil which is liquid at 20 ° C. and 1013 hPa is present in a total amount of from 1 to 95% by weight, preferably from 10 to 85% by weight, preferably from 20 to 75% by weight. -%, more preferably from 35 to 70 wt .-%, in particular from 50 to 60 wt .-%, based on the total weight of the antiperspirant cosmetic agent is included.
  • the antiperspirant compositions according to the invention less than 0.2 wt .-%, preferably less than 0.1 wt .-%, in particular 0 wt .-% of at 20 ° C and 1013 hPa containing liquid cosmetic oil.
  • the use of only extremely small amounts of the cosmetic oil which is liquid at 20 ° C. and 1013 hPa is particularly preferred in the case of antiperspirant cosmetic agents according to the invention which are present in aqueous, aqueous-alcoholic or aqueous-glycolic form.
  • the fragrance is selected from the group of
  • esters in particular benzyl acetate, phenoxyethyl isobutyrate, p-tert-butylcyclohexyl acetate, lactyl acetate, dimethylbenzylcarbinylacetate (DMBCA), phenylethylacetate, benzylacetate, ethylmethylphenylglycinate, allylcyclohexylpropionate, styrallylpropionate, benzylsalicylate, cyclohexylsalicylate, floramate, melusate and jasmecyclate;
  • DMBCA dimethylbenzylcarbinylacetate
  • aldehydes especially linear alkanals of 8 to 18 carbon atoms, citral, citronellal, citronellyloxy-acetaldehyde, cyclamen aldehyde, lilial and bourgeonal;
  • ketones especially ionone, alpha-isomethylionone and methyl cedryl ketone
  • alcohols especially anethole, citronellol, eugenol, geraniol, linalool, phenylethyl alcohol and terpineol;
  • hydrocarbons in particular terpenes such as limonene and pinene; such as
  • mixtures of different fragrances are preferably used, which together produce an appealing scent.
  • Particularly pleasing antiperspirant cosmetic agents according to the invention are obtained when the perfume in a total amount of 0.00001 to 10 wt .-%, preferably from 0.001 to 9 wt .-%, preferably from 0.01 to 8 wt .-%, further preferably from 0.5 to 7 wt .-%, in particular from 1 to 6 wt .-%, based on the total weight of the antiperspirant cosmetic agent is included.
  • the fragrance in a total amount of 0.00001 to 5% by weight, preferably 0.001 to 4 wt .-%, preferably 0.01 to 3 wt .-%, more preferably 0 , 1 to 2 wt .-%, in particular 0.2 to 1, 5 wt .-%, based on the total weight of the blowing agent-containing antiperspirant cosmetic agent is included.
  • the wax is selected from the group of
  • esters of saturated, monohydric Cs -is alcohols with saturated C 12 -is monocarboxylic acids (iii) esters of saturated, monohydric Cs -is alcohols with saturated C 12 -is monocarboxylic acids;
  • esters of a saturated, monohydric C 16 -C 6 alkanol and a saturated C 12 -C 36 monocarboxylic acid in particular cetyl behenate, stearyl behenate and C 20 -C 40 -alkyl stearate;
  • glycerol triesters of saturated linear C 12 -C 30 carboxylic acids which may be hydroxylated, in particular hydrogenated palm oil, hydrogenated coconut oil, hydrogenated castor oil, glyceryl tribehenate and glyceryl tri-12-hydroxy stearate;
  • animal waxes in particular beeswax, shellac wax and spermaceti;
  • (ix) synthetic waxes in particular montan ester waxes, hydrogenated jojoba waxes and sasol waxes, polyalkylene waxes and polyethylene glycol waxes, C 2o-C4o dialkyl esters of dimer acids, C 30 -so-alkyl beeswax, and alkyl and alkylaryl esters of dimer fatty acids, paraffin waxes; such as
  • esters of saturated, monohydric Ci2-is alcohols with saturated Ci2 -is monocarboxylic acids are stearyl laurate, cetearyl stearate (eg Crodamol® CSS), cetyl palmitate (eg Cutina® CP) and myristyl myristate (eg Cetiol® MM).
  • cetearyl stearate eg Crodamol® CSS
  • cetyl palmitate eg Cutina® CP
  • myristyl myristate eg Cetiol® MM
  • a C2o-C4o-alkyl stearate is preferably used as the wax component.
  • This ester is known under the name Kester ® K82H or Kesterwachs ® K80H and is sold by Koster Keunen Inc..
  • the wax in a total amount of 0.01 to 20 wt .-%, preferably from 3 to 20 wt .-%, preferably from 5 to 18 wt .-%, in particular from 6 to 15 wt .-%, based on the total weight of the antiperspirant cosmetic agent is included.
  • a particularly good antiperspirant effect is obtained in the context of the present invention, when the antiperspirant aluminum salt in a total amount of 2 to 40% by weight, preferably from 3 to 35 wt .-%, preferably from 4 to 32 wt .-%, further preferably from 5 to 28 wt .-%, more preferably from 8 to 25 wt .-%, in particular from 12 to 22 wt .-%, based on the total weight of the antiperspirant cosmetic agent is included.
  • the antiperspirant aluminum salt in a total amount of 0, 1 to 20 wt .-%, preferably from 0.5 to 15 wt .-%, preferably from 1 to 12 wt .-%, more preferably from 1, 5 to 10 wt .-%, in particular from 2 to 8 wt .-%, based on the total weight of the blowing agent-containing antiperspirant composition is included.
  • the antiperspirant aluminum salt may be selected from the group of
  • water-soluble astringent inorganic salts of aluminum especially aluminum chlorohydrate, aluminum sesquichlorohydrate, aluminum dichlorohydrate, aluminum hydroxide, potassium aluminum sulfate, aluminum bromohydrate, aluminum chloride, aluminum sulfate;
  • water-soluble astringent organic salts of aluminum in particular aluminum chlorohydrex-propylene glycol, aluminum chlorohydrex-polyethylene glycol, aluminum-propylene glycol complexes, aluminum sesquichlorohydrex-propylene glycol, aluminum sesquichlorohydrex-polyethylene glycol, aluminum-propylene glycol-dichlorhydrex, aluminum-polyethylene glycol-dichlorohydrex, aluminum undecylenoyl collagen amino acid Sodium aluminum lactate, sodium aluminum chlorhydroxactate, aluminum lipoamino acids, aluminum lactate, aluminum chlorohydroxy allantoinate, sodium aluminum chlorohydroxy lactate;
  • water-soluble astringent inorganic aluminum-zirconium salts especially aluminum zirconium trichlorohydrate, aluminum zirconium tetrachlorohydrate, aluminum zirconium pentachlorohydrate, aluminum zirconium octachlorohydrate;
  • water-soluble astringent organic aluminum-zirconium salts especially aluminum zirconium-propylene glycol complexes, aluminum zirconium trichlorohydrex glycine, aluminum zirconium tetrachlorohydrex glycine, aluminum zirconium pentachlorohydrex glycine, aluminum zirconium octachlorohydrex glycine; such as
  • water-soluble aluminum salts are understood to mean those salts which have a solubility of at least 3% by weight at 20 ° C., ie at least 3 g of the antiperspirant dissolve Aluminum salt in 97 g of water at 20 ° C.
  • Particularly preferred inorganic aluminum salts are chosen from aluminum chlorohydrate, aluminum chlorohydrate, in particular having the general formula [Al2 (OH) 5 Cl ⁇ hbOJn 1-6, preferably [Al 2 (OH) 5 Cl ⁇ 2-3 hbOJn which (in non-activated (polymerized) or in an activated depolymerized) form, and aluminum chlorohydrate having the general formula [Al 2 (OH) 4Cl 2 ⁇ 1- 6 hhOJn, preferably [Al 2 (OH) 4Cl 2 ⁇ 2-3 hbOJn, in non-activated (polymerized) or in activated (depolymerized ) Form may be present.
  • the preparation of such antiperspirant aluminum salts is disclosed, for example, in US 3,887,692 A, US 3,904,741 A, US 4,359,456 A, GB 2 048 229 A and GB 1 347 950 A.
  • antiperspirant aluminum salts are selected from so-called “activated” aluminum salts, which are also referred to as “antiperspirant active ingredients” with enhanced activity (English: enhanced activity). Such agents are known in the art and are also commercially available. Their preparation is disclosed, for example, in the publications GB 2 048 229 A, US Pat. Nos. 4,775,528 and 6,010,688.
  • Activated aluminum salts are typically produced by heat-treating a dilute solution of the appropriate salt (eg, a 10 wt.% Salt solution) to increase its HPLC peak 4-to-peak 3 area ratio. The activated salt can then be dried to a powder, in particular spray-dried. In addition to the spray drying z. B. also suitable for roller drying.
  • Activated aluminum salts typically have an HPLC peak 4-to-peak 3 area ratio of at least 0.4, preferably at least 0.7, especially at least 0.9, with at least 70% of the aluminum attributable to these HPLC peaks.
  • activated aluminum zirconium salts which have a high HPLC peak 5 aluminum content, in particular a peak 5 area of at least 33%, preferably of at least 45%, based on the total area under the peaks 2 to 5, measured by HPLC of a 10% by weight aqueous solution of the active ingredient under conditions in which the aluminum species are resolved into at least 4 successive peaks (denoted peaks 2 to 5)
  • Preferred aluminum-zirconium salts of high HPLC peak 5-aluminum content (also referred to as "E 5 AZCH”) is disclosed, for example, in US 6 436 381 A and US 6 649 152 A.
  • the abovementioned activated aluminum-zirconium salt may additionally be treated with a water-soluble strontium salt and / or stabilized with a water-soluble calcium salt, as disclosed, for example, in US Pat. No. 6,923,952 A.
  • antiperspirant aluminum salts as nonaqueous solutions or solubilisates of an activated antiperspirant aluminum or aluminum zirconium salt, for example in accordance with US Pat. No. 6,010,688 A.
  • Such aluminum or aluminum zirconium salts are stabilized by the addition of an effective amount of a polyhydric alcohol having 3 to 6 carbon atoms and 3 to 6 hydroxyl groups, preferably propylene glycol, sorbitol and pentaerythritol, against the loss of activation of the salt.
  • complexes of activated aluminum or aluminum-zirconium antiperspirant salts with a polyhydric alcohol containing from 20 to 50% by weight, preferably from 20 to 42% by weight, activated antiperspirant aluminum or aluminum zirconium salt and from 2 to 16 Wt .-% molecularly bound water, the remainder to 100 wt .-% is at least one polyhydric alcohol having 3 to 6 carbon atoms and 3 to 6 hydroxyl groups.
  • Propylene glycol, propylene glycol / sorbitol mixtures and propylene glycol / pentaerythritol mixtures are preferred such alcohols.
  • Such inventively preferred complexes of an activated antiperspirant aluminum or aluminum zirconium salt with a polyhydric alcohol are, for. For example, in documents US 5,643,558 A and US 6,245,325.
  • antiperspirant aluminum salts of basic calcium aluminum salts as z.
  • these salts can be prepared by reaction of calcium carbonate with aluminum chlorohydrate or aluminum chloride and aluminum powder or by adding Calcium chloride dihydrate are obtained to aluminum chlorhydroxide.
  • aluminum-zirconium complexes which are buffered with salts of amino acids, in particular with alkali and Erdalkaliglycinaten, and as such.
  • use As disclosed in the document US 4 017 599 A, use.
  • activated aluminum salts are those of the general formula Al 2 (OH) 6- a Xa, where X is Cl, Br, I or NO 3 and "a" is a number from 0.3 to 5, preferably from 0.8 to 2, 5 is in particular from 1 to 2, so that the molar ratio of Al: X 0.9: 1 to 2, 1: 1.
  • Such activated antiperspirant aluminum salts are disclosed, for example, in US Pat. No. 6,074,632.
  • Preferred activated aluminum-zirconium salts are those of the general formula ZrO (OH) 2-P BYB, wherein Y is Cl, Br, I, NO3 or SO4, b is a rational number from 0.8 to 2 and p is the valence of Y is such that the Al: Zr molar ratio is from 2 to 10 and the metal: (X + Y) ratio is from 0.73 to 1.2, preferably from 0.9 to 1.5.
  • Such activated antiperspirant aluminum zirconium salts are disclosed, for example, in the aforementioned US Pat. No. 6,074,632.
  • a particularly preferred salt is aluminum-zirconium chlorohydrate (i.e., X and Y are Cl), which has an Al: Zr ratio of 2 to 10 and a molar metal: Cl ratio of 0.9 to 2.1.
  • Preferred antiperspirant active compounds are disclosed in US 6,663,854 A and US 2004/0009133 A1.
  • Particularly preferred antiperspirant aluminum salts according to the invention have a molar metal-to-chloride ratio of 1.9 to 1.2.
  • the metal-to-chloride ratio of aluminum sesquichlorohydrates which is also particularly preferred in the invention is from 1.5: 1 to 1.8: 1.
  • Preferred aluminum-zirconium tetrachlorohydrates have a molar ratio of Al: Zr of from 2 to 6 and of metal: chloride of from 0.9 to 1 .3, in particular salts having a molar metal-to-chloride ratio of from 0.9 to 1.1 , preferably from 0.9 to 1.0 are preferred.
  • a particularly high activity and significantly improved stabilization of the antiperspirant aluminum salt is achieved if the alpha-hydroxy acid is used in a total amount of from 0.05 to 8% by weight, preferably from 0.1 to 7% by weight. , preferably from 0.3 to 5 wt .-%, more preferably from 0.5 to 3 wt .-%, still more preferably from 0.8 to 2.5 wt .-%, in particular from 1 to 2 wt. %, based on the total weight of the antiperspirant cosmetic agent.
  • the antiperspirant cosmetic agents may contain the alpha-hydroxy acid in a total amount of 0.05 to 20% by weight, preferably 0.3 to 18% by weight, preferably 0.5 to 15 Wt .-%, more preferably from 0.7 to 10 wt .-%, even more preferably from 1, 0 to 9 wt .-%, in particular from 1, 5 to 6 wt .-%, based on the total weight of the blowing agent-containing antiperspirant cosmetic agent.
  • the use of the abovementioned amount (s) of the alpha-hydroxy acid (s) results in a significantly increased formation of short-chain polymers of the antiperspirant aluminum salt and thus in an improved antiperspirant effect.
  • the short-chain polymers of the antiperspirant aluminum salt are effectively stabilized over a long period of time, so that the use of the alpha-hydroxy acid in the amounts listed above results in a significantly improved antiperspirant effect even after prolonged storage.
  • the antiperspirant cosmetic agent contains at least one alpha-hydroxy acid of -la) and / or (HS-1b) and / or (HS-1c) and / or (HS-ld ) and / or (HS-le)
  • Y + stands for Li + , Na + , 7 2 Mg 2+ , 7 2 Ca 2+ , 7 2 Mn 2+ , V 2 Zn 2+ , V 3 Al 3+ , 7 Zr 4 * or at least one antiperspirant aluminum salt,
  • X + for H + Li + , Na + , K + , NH 4 + , V 2 Mg 2+ , V 2 Ca 2+ , V 2 Mn 2+ , V 2 Zn 2+ , V 3 Al 3+ , V Zr 4 * or at least one antiperspirant aluminum salt, and
  • Z + for Li + , Na + , K + , NH 4 + , V 2 Mg 2+ , V 2 Ca 2+ , V 2 Mn 2+ , V 2 Zn 2+ , V 3 Al 3+ , V Zr 4 * or at least one antiperspirant aluminum salt is, contains.
  • the antiperspirant effect of the antiperspirant cosmetic agents of the present invention can be further improved if the antiperspirant cosmetic agent has a weight ratio of the antiperspirant aluminum salt to the alpha-hydroxy acid of 40: 1 to 19: 1, preferably 30: 1 to 16: 1, preferably 20: From 1 to 15: 1, more preferably from 10: 1 to 13: 1, even more preferably from 9: 1 to 12: 1, in particular from 8: 1 to 1: 1.
  • the above-mentioned weight ratio refers to the total amount of all antiperspirant aluminum salts and the total amount of all alpha-hydroxy acids in the antiperspirant cosmetic agent.
  • the weight ratio of the antiperspirant aluminum salt to the alpha-hydroxy acid is 5: 1.
  • the use of a weight ratio of the antiperspirant aluminum salt to the alpha-hydroxy acid of 10: 1 leads to antiperspirant cosmetic agents according to the invention, which are excellent Have antiperspirant activity and no significant deterioration of the antiperspirant effect occurs even after long storage periods.
  • protic solvents in particular in high concentrations or amounts, can be used without the antiperspirant effect of the antiperspirant cosmetic agents according to the invention being adversely affected, so that an extremely flexible formulation of the compositions according to the invention is possible.
  • the antiperspirant cosmetic agent contains no zirconium-containing compounds.
  • the inventive avoidance of the use of zirconium-containing antiperspirant compounds, such as zirconium-aluminum mixed salts results in the cost-effective provision of the antiperspirant cosmetic agents of the invention, since the raw materials for the production of zirconium-containing compounds have higher prices.
  • the antiperspirant cosmetic agent preferably contains free water in a total amount of less than 10% by weight, preferably less than 8% by weight, preferably less than 5% by weight, more preferably less than 3% by weight. even more preferably less than 1% by weight, in particular 0% by weight, based on the total weight of the antiperspirant cosmetic agent.
  • free water is thus understood to mean water which is different from water of crystallization, water of hydration or similar molecularly bound water of the constituents used, in particular the antiperspirant aluminum salts.
  • the antiperspirant cosmetic agent therefore contains free water in a total amount of 15 to 96 wt .-%, preferably from 25 to 80 wt .-%, preferably from 30 to 70 wt .-%, in particular of 40 to 60 wt .-%, based on the total weight of the antiperspirant cosmetic agent.
  • the antiperspirant cosmetic agents according to the invention are preferably in the form of a suspension of the undissolved antiperspirant aluminum salt in the cosmetic oil which is liquid at 20 ° C. and 1 .013 hPa.
  • the antiperspirant cosmetic agent is present as a water-in-oil emulsion.
  • This may in particular be a sprayable water-in-oil emulsion which can be sprayed by means of a propellant.
  • the present invention in the form of a water-in-oil emulsion antiperspirant cosmetic agent, the alpha-hydroxy acid in a total amount of 0.05 to 8 wt .-%, preferably from 0.1 to 7 wt %, preferably from 0.3 to 5% by weight, more preferably from 0.5 to 3% by weight, still more preferably from 0.8 to 2.5% by weight, most preferably from 1 to 2 wt .-%, based on the total weight of the antiperspirant cosmetic agent contains.
  • the antiperspirant cosmetic agent is present as an oil-in-water emulsion.
  • the agent according to the invention is preferably sprayed as a propellant-free pump spray or squish spray or applied as a roll-on.
  • the present in the form of an oil-in-water emulsion antiperspirant cosmetic agent the alpha-hydroxy acid in a total amount of 0.05 to 8 wt .-%, preferably from 0.1 to 7 wt.
  • % preferably from 0.3 to 5% by weight, more preferably from 0.5 to 3% by weight, even more preferably from 0.8 to 2.5% by weight, in particular from 1 to 2 wt .-%, based on the total weight of the antiperspirant cosmetic agent contains.
  • the antiperspirant cosmetic agent is present as an aqueous, aqueous-alcoholic or aqueous-glycolic solution.
  • a sweat-inhibiting aluminum salt with an alpha-hydroxy acid even in protic solvents, such as aqueous solutions, high amounts of activated aluminum salt can be formed or stabilized, so that according to the invention the use of aqueous antiperspirant cosmetic agents is also possible without a Deactivation of the antiperspirant aluminum salts and thus a significant reduction in the antiperspirant effect occurs.
  • the antiperspirant cosmetic agent contains ethanol in a total amount of 1 to 50 wt .-%, preferably from 5 to 40 wt .-%, preferably from 7 to 35 wt .-%, in particular from 10 to 30 Wt .-%, based on the total weight of the antiperspirant cosmetic agent.
  • the antiperspirant cosmetic agent ethanol in a total amount of 10 to 95 wt .-%, preferably from 15 to 90 wt .-%, preferably from 20 to 87 wt .-%, more preferably from 30 to 85 wt .-%, in particular from 40 to 80 wt .-%, based on the total weight of the antiperspirant cosmetic agent contains.
  • the use of the alpha-hydroxy acid itself can utilize high levels of protic solvents, such as ethanol, without adversely affecting the activation or stabilization of the short-chain polymers of the antiperspirant aluminum salt.
  • the antiperspirant cosmetic agent is formulated as a spray application.
  • the spray application is carried out with a spray device which contains a filling of the liquid, viscous-flowable, suspension-shaped or powdered antiperspirant cosmetic agent according to the invention in a container.
  • the filling may be under the pressure of a propellant (compressed gas cans, compressed gas packages, aerosol dispensers), or it may be a mechanically operated pump sprayer without propellant (pump sprays / squeeze bottle).
  • the containers have a removal device, preferably in the form of valves, which allow the removal of the contents as a mist, smoke, foam, powder, paste or liquid jet.
  • containers for the spray devices are mainly cylindrical vessels made of metal (aluminum, tinplate, volume preferably a maximum of 1,000 ml), protected or non-splitterndem glass or plastic (volume preferably a maximum of 220 ml) or splintering glass or plastic (volume preferably 50th to 400 ml) in question.
  • Creamy, gelatinous, pasty and liquid agents may be packaged, for example, in pump, spray or squeeze dispensers, in particular in multi-chamber pumping, multi-chamber spray or multi-chamber squeeze dispensers.
  • the Packaging for the compositions according to the invention may be opaque, but also transparent or translucent.
  • the antiperspirant cosmetic is preferably formulated as a stick, soft solid, cream, roll-on, dibenzylidenalditol-based gel, loose or compact powder.
  • the formulation of the antiperspirant cosmetic agents according to the invention in a particular dosage form such as, for example, an antiperspirant roll-on, an antiperspirant stick or an antiperspirant gel, preferably conforms to the requirements of the intended use.
  • the antiperspirant cosmetic agents according to the invention can therefore be present in solid, semisolid, liquid, disperse, emulsified, suspended, gelatinous, multiphase or powdery form.
  • the term liquid also includes any types of solid dispersions in liquids.
  • multiphase antiperspirant cosmetic agents are also understood to mean agents which have at least two different phases with a phase separation and in which the phases can be arranged horizontally, ie one above the other, or vertically, ie side by side.
  • the application can be done, for example, with a roller ball applicator.
  • Such scooters have a ball mounted in a ball bed which can be moved by movement over a surface. The ball picks up some of the sweat-inhibiting agent to be distributed and conveys it to the surface to be treated.
  • the packaging for the compositions according to the invention can, as stated above, be opaque, transparent or translucent.
  • the antiperspirant cosmetic agent is contained on and / or in a disposable substrate selected from the group of wipes, pads and bulbs.
  • a disposable substrate selected from the group of wipes, pads and bulbs.
  • wet wipes ie prefabricated for the user, preferably individually packaged, wet wipes, as they are for. B. from the field of glass cleaning or from the field of wet toilet paper are well known.
  • Such wet wipes which can advantageously also contain preservatives, are impregnated or applied with an antiperspirant cosmetic agent according to the invention and preferably individually packaged. You can z. B. be used as a deodorant cloth, which is particularly interesting for use on the go.
  • Preferred substrate materials are selected from porous sheet-like cloths.
  • wipes can be made of a fibrous or cellular flexible material which has sufficient mechanical stability and softness for application to the skin.
  • wipes include wipes made of woven and nonwoven (nonwoven) synthetic and natural fibers, felt, paper or foam, such as hydrophilic polyurethane foam.
  • Deodorizing or antiperspirant substrates which are preferred according to the invention can be obtained by impregnation or impregnation or else by melting a perspiration-inhibiting cosmetic agent according to the invention onto a substrate.
  • the antiperspirant cosmetic agents of the present invention may further contain other adjuvants.
  • the antiperspirant cosmetic agents according to the invention preferably contain at least one wide adjuvant selected from the group of (i) emulsifiers and / or surfactants; (ii) hydrogel formers; (iii) chelating agents; (iv) deodorant agents; (v) monohydric and / or polyhydric alcohols and / or polyethylene glycols; (vi) skin-cooling agents; (vii) propellants; (viii) thickeners and (ix) their mixtures.
  • Emulsifiers and surfactants which are preferably suitable according to the invention are selected from anionic, cationic, nonionic, amphoteric, in particular ampholytic and zwitterionic emulsifiers and surfactants.
  • Surfactants are amphiphilic (bifunctional) compounds which consist of at least one hydrophobic and at least one hydrophilic moiety.
  • the hydrophobic moiety is preferably a hydrocarbon chain of 8 to 28 carbon atoms, which may be saturated or unsaturated, linear or branched. Most preferably, this C8-C28 alkyl chain is linear.
  • anionic surfactants surfactants with exclusively anionic charges; they contain z.
  • carboxyl groups sulfonic acid groups or sulfate groups.
  • Particularly preferred anionic surfactants are alkyl sulfates, alkyl ether sulfates, acyl glutamates and Cs-24 carboxylic acids and their salts, the so-called soaps.
  • Cationic surfactants are understood as meaning surfactants with exclusively cationic charges; they contain z.
  • Preferred esterquats are quaternized ester salts of fatty acids with triethanolamine, quaternized ester salts of fatty acids with diethanolalkylamines and quaternized ester salts of fatty acids with 1,2-dihydroxypropyldialkylamines.
  • amphoteric surfactants are subdivided into ampholytic surfactants and zwitterionic surfactants.
  • Ampholytic surfactants are understood as meaning those surface-active compounds which have both acidic (for example -COOH or -SO 3 H groups) and basic hydrophilic groups (for example amino groups) and thus behave acidic or basic depending on the condition.
  • Zwitterionic surfactants are understood by the person skilled in the art to be surfactants which carry both a negative and a positive charge in the same molecule.
  • Zwitterionic surfactants are the betaines, the N-alkyl-N, N-dimethylammonium glycinates, the N-acyl-aminopropyl-N, N-dimethylammoniumglycinate and the 2-alkyl-3-carboxymethyl-3-hydroxyethyl imidazoline with 8 to 24 carbon atoms in the alkyl group.
  • ampholytic surfactants are N-alkylglycines, N-alkylaminopropionic acids, N-alkylaminobutyric acids, N-alkyliminodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids and alkylaminoacetic acids each having 8 to 24 Carbon atoms in the alkyl group
  • compositions according to the invention which are formulated as an emulsion, in particular as an oil-in-water emulsion, preferably comprise at least one nonionic oil-in-water emulsifier having an HLB value of more than 7 to 20.
  • nonionic oil-in-water emulsifier having an HLB value of more than 7 to 20.
  • L is the weight fraction of the lipophilic groups, that is the fatty alkyl or fatty acyl groups, in the ethylene oxide adducts, expressed in weight percent.
  • a water-in-oil emulsifier having an HLB value of greater than 1.0 and less than or equal to 7.0 is used.
  • Nonionic oil-in-water emulsifiers suitable for the purposes of the present invention and suitable nonionic water-in-oil emulsifiers are described, for example, in German Offenlegungsschrift DE 10 2006 004 957 A1.
  • hydrogel-forming substances which are selected from cellulose ethers, especially hydroxyalkylcelluloses, in particular hydroxypropylcellulose, hydroxypropylmethylcellulose, hydroxyethylcellulose, carboxymethylcellulose, cetylhydroxyethylcellulose, hydroxybutylmethylcellulose, methylhydroxyethylcellulose, furthermore xanthan gum, sclerotium gum , Succinoglucans, polygalactomannans, in particular guar gums and locust bean gum, in particular guar gum and locust bean gum itself and the nonionic hydroxyalkyl guar derivatives and locust bean gum derivatives, such as hydroxypropyl guar, carboxymethylhydroxypropyl guar, hydroxypropylmethyl guar, hydroxyethyl guar and Carboxymethylguar, pectins, agar, carrageenan, tragacanth, gum arabic
  • hydrogel formers are selected from cellulose ethers, in particular from hydroxyalkylcelluloses, in particular from hydroxypropylcellulose, hydroxypropylmethylcellulose, hydroxyethylcellulose, carboxymethylcellulose, cetylhydroxyethylcellulose, hydroxybutylmethylcellulose and methylhydroxyethylcellulose, and mixtures thereof. Hydroxyethyl cellulose is preferably used as hydrogel former.
  • At least one chelating agent according to the invention selected from ethylenediaminetetraacetic acid (EDTA) and its salts and nitrilotriacetic acid (NTA) and mixtures thereof Substances, in a total amount of 0.01 to 0.5 wt .-%, preferably from 0.02 to 0.3 wt .-%, in particular from 0.05 to 0.1% by weight, based on the total weight of the antiperspirant agent according to the invention.
  • chelating agents which are selected from the group consisting of ⁇ -alaninediacetic acid, cyclodextrin, diethylenetriaminepentamethylenephosphonic acid, sodium, potassium, calcium disodium, ammonium and triethanolamine salts of ethylenediaminetetraacetic acid (EDTA), etidronic acid, hydroxyethylethylenediaminetetraacetic acid (HEDTA) and their sodium salts, sodium salts of nitrilotriacetic acid (NTA), diethylenetriaminepentaacetic acid, phytic acid,
  • Tetrasodiumiminodisuccinate Tetrasodiumiminodisuccinate, trisodium ethylenediamine disuccinate and desferrioxamine.
  • the antiperspirant effect of the antiperspirant cosmetic agents according to the invention can be further increased if at least one deodorant active ingredient in a total amount of 0.0001 to 40 wt .-%, preferably from 0.2 to 20 wt .-%, preferably from 1 to 15 wt .-%, in particular from 1, 5 to 5 wt .-%, based on the total weight of the antiperspirant cosmetic agent according to the invention, is included. If ethanol is used in the compositions according to the invention, this does not apply in the context of the present invention as a deodorant active ingredient, but as a constituent of the carrier.
  • Deodorant agents which are preferred according to the invention are selected from the group of (i) silver salts; (ii) aromatic alcohols, in particular 2-benzylheptan-1-ol and mixtures of 2-benzylheptan-1-ol and phenoxyethanol; (iii) 1,2-alkanediols having 5 to 12 carbon atoms, especially 3- (2-ethylhexyloxy) -1, 2-propanediol; (iv) triethyl citrate; (v) agents against exoesterases, especially against arylsulfatase, lipase, beta-glucuronidase and cystathion-beta-lyase; (vi) cationic phospholipids; (vii) odor absorbers, in particular silicates, such as montmorillonite, kaolinite, IIit, beidellite, nontronite, saponite, hectorite, bentonite, smectite and tal
  • Preferred antiperspirant cosmetic agents according to the invention also contain at least one water-soluble polyhydric C 2-9 -alkanol having 2 to 6 hydroxyl groups and / or at least one water-soluble polyethylene glycol having 3 to 50 ethylene oxide units and mixtures thereof. This does not include the abovementioned deodorant active ingredients in the form of 1, 2-alkanediols.
  • Preferred alkanols are selected from 1,2-propylene glycol, 2-methyl-1,3-propanediol, glycerol, 1,2-butylene glycol, 1,3-butylene glycol, 1,4-butylene glycol, and pentylene glycols, such as 1,2-pentanediol and 1, 5-pentanediol, hexanediols such as 1, 2-hexanediol and 1, 6-hexanediol, hexanetriols such as 1, 2,6-hexanetriol, 1, 2-octanediol, 1, 8-octanediol, dipropylene glycol, tripropylene glycol, diglycerol, triglycerol , Erythritol, sorbitol, cis-1,4-dimethylolcyclohexane, trans-1,4-dimethylolcyclohexane, any mixture
  • Suitable water-soluble polyethylene glycols are selected from PEG-3, PEG-4, PEG-6, PEG-7, PEG-8, PEG-9, PEG-10, PEG-12, PEG-14, PEG-16, PEG-18 and PEG-20 and mixtures thereof, with PEG-3 to PEG-8 being preferred.
  • the antiperspirant cosmetic agents further contain at least one skin-cooling agent.
  • Skin-cooling active ingredients suitable according to the invention are, for example, menthol, isopulegol and menthol derivatives, eg. Menthyl lactate, menthyl glycolate, menthyl ethyl oxamate, menthyl pyrrolidone carboxylic acid, menthyl methyl ether, menthoxy propane diol, menthone glycerol acetal (9-methyl-6- (1-methylethyl) -1, 4-dioxaspiro (4.5) decane-2-methanol), mono-menthyl succinate, 2-hydroxymethyl -3,5,5-trimethylcyclohexanol and 5-methyl-2- (1-methylethyl) cyclohexyl-N-ethyloxamate.
  • Preferred skin-cooling active ingredients are menthol, isopulegol, menthyl lactate, menthoxypropanediol, menthylpyrrolidonecarboxylic acid and 5-methyl-2- (1-methylethyl) cyclohexyl-N-ethyloxamate, as well as mixtures of these substances, in particular mixtures of menthol and menthyl lactate, menthol, menthol glycolate and menthyl lactate, menthol and menthoxypropanediol or menthol and isopulegol.
  • the antiperspirant cosmetic agents according to the invention contain a propellant.
  • propellants are propane, propene, n-butane, isobutane, isobutene, n-pentane, pentene, isopentane, isopentene, methane, ethane, dimethyl ether, nitrogen, air, oxygen, nitrous oxide, 1, 1, 1, 3-tetrafluoroethane, heptafluoro-n-propane, perfluoroethane, monochlorodifluoromethane, 1,1-difluoroethane, tetrafluoropropenes, both individually and in their mixtures.
  • hydrophilic propellants such as carbon dioxide
  • hydrophilic propellants such as carbon dioxide
  • lipophilic propellant gas eg., Propane / butane
  • propane, n-butane, isobutane and mixtures of these propellants propane, n-butane, isobutane and mixtures of these propellants. It has been found that the use of n-butane as the only propellant gas according to the invention can be particularly preferred.
  • the total amount of the blowing agent is 20 to 95 wt.%, Preferably 30 to 85 wt.%, In particular 40 to 75 wt .-%, each based on the total weight of Antiperspirants, consisting of the antiperspirant cosmetic agent according to the invention and the propellant.
  • the total amount of blowing agent 1 to 95 wt .-%, preferably 2 to 85 wt .-%, in particular 3 to 75 wt .-%, .-%, each based on the total weight of Antiperspirant, consisting of the antiperspirant cosmetic agent of the invention and the propellant is.
  • lipophilic thickeners can furthermore be used according to the invention.
  • the at least one antiperspirant aluminum salt is suspended undissolved in at least one at 20 ° C and 1013 hPa liquid cosmetic oil.
  • at least one lipophilic thickener may be added to this suspension as a suspending aid.
  • Lipophilic thickeners preferred according to the invention are selected from hydrophobized clay minerals and fumed silicic acids.
  • the antiperspirant cosmetic agents according to the invention are characterized in that they are formulated as a water-in-oil emulsion and - based on the total weight of the antiperspirant cosmetic agent according to the invention - at least one antiperspirant aluminum salt in a total amount of 2 to 75 wt.
  • wt .-% preferably 3 to 70 wt .-%, preferably 4 to 65 wt .-%, more preferably 5 to 55 wt .-%, even more preferably 8 to 40 wt .-%, in particular 10 to 30 wt .-% , at least one alpha-hydroxy acid in a total amount of 0.05 to 8 wt .-%, preferably 0.1 to 7 wt .-%, preferably 0.3 to 5 wt .-%, more preferably 0.5 to 3 Wt .-%, even more preferably 0.8 to 2.5 wt .-%, in particular 1 to 2 wt .-%, 12 to 90 wt .-%, preferably 25 to 55 wt .-%, preferably 30 to 50 Wt .-%, in particular 35 to 45 wt .-% water,
  • the antiperspirant cosmetic agents according to the invention are characterized in that they are formulated as an oil-in-water emulsion and - based on the total weight of the antiperspirant cosmetic agent according to the invention - at least one antiperspirant aluminum salt in a total amount of 2 to 75 wt %, preferably 3 to 70% by weight, preferably 4 to 65% by weight, more preferably 5 to 55% by weight, even more preferably 8 to 40% by weight, in particular 10 to 30% by weight.
  • % at least one alpha-hydroxy acid in a total amount of 0.05 to 8 wt .-%, preferably 0.1 to 7 wt .-%, preferably 0.3 to 5 wt .-%, more preferably 0.5 to 3 wt .-%, still more preferably 0.8 to 2.5 wt .-%, in particular 1 to 2 wt .-%, From 15 to 90% by weight, preferably from 25 to 55% by weight, preferably from 30 to 50% by weight, in particular from 35 to 45% by weight, of water,
  • a further preferred embodiment of the present invention comprises antiperspirant cosmetic agents according to the invention, which are characterized in that they comprise, based on the total weight of the antiperspirant cosmetic agent according to the invention, at least one antiperspirant aluminum salt in a total amount of 2 to 75% by weight, preferably 3 to 70 wt .-%, preferably 4 to 65 wt .-%, more preferably 5 to 55 wt .-%, even more preferably 8 to 40 wt .-%, in particular 10 to 30 wt .-%, at least one alpha-hydroxy acid in a total amount of a total of 0.05 to 8 wt .-%, preferably 0.1 to 7 wt .-%, preferably 0.3 to 5 wt .-%, more preferably 0.5 to 3 wt .-%, still more preferably 0.8 to 2.5 wt .-%, in particular 1 to 2 wt .-%, 15 to 90 wt .-%, preferably 25
  • a further preferred embodiment of the present invention comprises antiperspirant cosmetic agents according to the invention, which are characterized in that they comprise, based on the total weight of the antiperspirant cosmetic agent according to the invention, at least one antiperspirant aluminum salt in a total amount of 2 to 75% by weight, preferably 3 to 70 wt .-%, preferably 4 to 65 wt .-%, more preferably 5 to 55 wt .-%, even more preferably 8 to 40 wt .-%, in particular 10 to 30 wt .-%, at least one alpha-hydroxy acid in a total amount of a total of 0.05 to 8 wt .-%, preferably 0.1 to 7 wt .-%, preferably 0.3 to 5 wt .-%, more preferably 0.5 to 3 wt .-%, still more preferably 0.8 to 2.5 wt .-%, in particular 1 to 2 wt .-%, 15 to 90 wt .-%, preferably 25
  • the antiperspirant cosmetic agents according to the invention have a dynamic viscosity in the range from 10 to 5000 mPas, preferably from 100 to 1000 mPas, preferably from 200 to 800 mPas, measured with a Brookfield viscometer, spindle RV 4, 20 s ⁇ without Helipath, at 20 ° C ambient temperature and 20 ° C sample temperature.
  • a further preferred embodiment of the present invention comprises antiperspirant cosmetic agents according to the invention, which are characterized in that they comprise, based on the total weight of the antiperspirant cosmetic agent according to the invention, at least one antiperspirant aluminum salt in a total amount of 2 to 75% by weight, preferably 3 to 70 wt .-%, preferably 4 to 65 wt .-%, more preferably 5 to 55 wt .-%, even more preferably 8 to 40 wt .-%, in particular 10 to 30 wt .-%, at least one alpha-hydroxy acid in a total amount of a total of 0.05 to 8 wt .-%, preferably 0.1 to 7 wt .-%, preferably 0.3 to 5 wt .-%, more preferably 0.5 to 3 wt .-%, still more preferably 0.8 to 2.5 wt .-%, in particular 1 to 2 wt .-%, 15 to 90 wt .-%, preferably 25
  • the antiperspirant cosmetic agents according to the invention have a dynamic viscosity in the range from 1000 to 800,000 mPas, preferably from 2,000 to 700,000 mPas, preferably from 3,000 to 500,000 mPas, measured with a Brookfield viscometer, spindle RV 4, 20 s 1 , without helipath, at 20 ° C ambient temperature and 20 ° C sample temperature.
  • the antiperspirant cosmetic agents according to the invention are characterized in that they are formulated as a water-in-oil emulsion and - based on the total weight of the antiperspirant cosmetic agent according to the invention - at least one antiperspirant aluminum salt in a total amount of 2 to 75 wt %, preferably 3 to 70% by weight, preferably 4 to 65% by weight, more preferably 5 to 55% by weight, even more preferably 8 to 40% by weight, in particular 10 to 30% by weight.
  • % at least one alpha-hydroxy acid in a total amount of 0.05 to 8 wt .-%, preferably 0.1 to 7 wt .-%, preferably 0.3 to 5 wt .-%, more preferably 0.5 to 3 wt .-%, still more preferably 0.8 to 2.5 wt .-%, in particular 1 to 2 wt .-%, 15 to 75 wt .-%, preferably 25 to 60 wt .-%, preferably 30 to 55 wt .-%, in particular 35 to 50 wt .-% water
  • the antiperspirant cosmetic agents according to the invention are characterized in that they are formulated as an oil-in-water emulsion and - based on the total weight of the antiperspirant cosmetic agent according to the invention - at least one antiperspirant aluminum salt in a total amount of 2 to 75 wt %, preferably 3 to 70% by weight, preferably 4 to 65% by weight, more preferably 5 to 55% by weight, even more preferably 8 to 40% by weight, in particular 10 to 30% by weight.
  • % at least one alpha-hydroxy acid in a total amount of 0.05 to 8 wt .-%, preferably 0.1 to 7 wt .-%, preferably 0.3 to 5 wt .-%, more preferably 0.5 to 3 wt .-%, more preferably 0.8 to 2.5 wt .-%, in particular 1 to 2 wt .-%, 15 to 90 wt .-%, preferably 25 to 80 wt .-%, preferably 30 to 75 wt .-%, in particular 40 to 60 Gew. -% water, and
  • wt .-% optionally 0.01 to 2 wt .-%, preferably 0, 1 to 1 wt .-%, preferably 0.2 to 0.7 wt .-%, in particular 0.3 to 0.5 wt .-% of a hydrogel containing forming substance.
  • a second object of the present invention is the use of a combination of at least one selected from the group of cosmetic oils which are liquid at 20 ° C and 1 .013 hPa, fragrances and waxes, at least one antiperspirant aluminum salt in a total amount of 1 to 80 wt .-%, based on the total weight of the combination, and at least one alpha-hydroxy acid of the formula (HS-I), (HS-II) and (HS-III)
  • R is a linear or branched alkyl group having 1 to 6 carbon atoms
  • R 2 , R 3 , R 4 and R 5 each independently represent hydrogen, -OH, a linear or branched alkyl group of 1 to 8 carbon atoms, an alkoxy group of 1 to 6
  • R 7 , R 8 , R 9 and R 0 each independently of one another, represent hydrogen, an alkoxy group having 1 to 6 carbon atoms or -OH,
  • y is a number from 0 to 5
  • X + for H + Li + , Na + , K + , NH 4 + , 7 2 Mg 2+ , 7 2 Ca 2+ , V 2 Mn 2+ , V 2 Zn 2+ , V 3 Al 3+ , V 4 Zr 4 "or at least one antiperspirant aluminum salt, and
  • Y + is Li + , Na + , V 2 Mg 2+ , V 2 Ca 2+ , V 2 Mn 2+ , V 2 Zn 2+ , V 3 Al 3+ , V 4 Zr 4 "or at least one antiperspirant aluminum salt .
  • X + is Li + , Na + , K + , NH 4 + , V 2 Mg 2+ , V 2 Ca 2+ , V 2 Mn 2+ , V 2 Zn 2+ , V 3 Al 3+ , 4 Zr 4 * or at least one antiperspirant aluminum salt when R 4 is a galactopyranose residue,
  • a third aspect of the present invention is a non-therapeutic cosmetic method for preventing and / or reducing transpiration of the body, which comprises an antiperspirant cosmetic agent containing at least one selected from the group of cosmetic oils at 20 ° C and 1,013 hPa liquid, fragrances and waxes, at least one antiperspirant aluminum salt in a total amount of 1 to 80 wt .-%, based on the total weight of the antiperspirant cosmetic agent, and at least one alpha-hydroxy acid, on the skin, in particular on the skin the armpits, is applied.
  • an antiperspirant cosmetic agent containing at least one selected from the group of cosmetic oils at 20 ° C and 1,013 hPa liquid, fragrances and waxes, at least one antiperspirant aluminum salt in a total amount of 1 to 80 wt .-%, based on the total weight of the antiperspirant cosmetic agent, and at least one alpha-hydroxy acid, on the skin, in particular on the skin the armpits, is applied.
  • a fourth subject of the present invention is the use of at least one alpha-hydroxy acid selected from one of the formulas (HS-I), (HS-II) and (HS-III)
  • R is a linear or branched alkyl group having 1 to 6 carbon atoms
  • R 7 , R 8 , R 9 and R 0 each independently of one another, represent hydrogen, an alkoxy group having 1 to 6 carbon atoms or -OH,
  • y is a number from 0 to 5
  • X + for H + Li + , Na + , K + , NH 4 + , 7 2 Mg 2+ , 7 2 Ca 2+ , V 2 Mn 2+ , V 2 Zn 2+ , V 3 Al 3+ , 7 Zr 4 * or at least one antiperspirant aluminum salt, and
  • Y + is Li + , Na + , V 2 Mg 2+ , V 2 Ca 2+ , V 2 Mn 2+ , V 2 Zn 2+ , V 3 Al 3+ , V Zr 4 * or at least one antiperspirant aluminum salt,
  • X + is Li + , Na + , K + , NH 4 + , V 2 Mg 2+ , V 2 Ca 2+ , V 2 Mn 2+ , V 2 Zn 2+ , V 3 Al 3+ , V Zr 4 * or at least one antiperspirant aluminum salt if R 4 is a galactopyranose residue,
  • Activation in the context of the present invention means the significantly increased formation of short-chain polymers of the antiperspirant aluminum salt when using alpha-hydroxy acid (s).
  • Stabilization in the context of the present invention furthermore refers to the avoidance or significant slowing down of the reformation of high-chain polymers from the short-chain polymers of the antiperspirant aluminum salts formed during the activation.
  • alpha-hydroxy acids By using special alpha-hydroxy acids, it has surprisingly been possible to significantly increase the activity of antiperspirant aluminum salts even over a longer storage period. Without wishing to be limited by this theory, the use of alpha-hydroxy acid (s) achieves a significant increase in the proportion of short-chain species of the antiperspirant aluminum salts. Furthermore, the thus formed short-chain species are excellently stabilized by the aforementioned alpha-hydroxy acids, so that an improved antiperspirant effect is ensured over a long period of time.
  • a particularly good activation and / or stabilization of the at least one antiperspirant aluminum salt is achieved if the alpha-hydroxy acid in a total amount of 0.01 to 50 wt .-%, preferably from 0, 1 to 40 wt .-%, preferably from 0 , 5 to 30 wt .-%, more preferably from 1 to 20 wt .-%, even more preferably from 1, 5 to 10% by weight, in particular from 2 to 7 wt .-%, based on the total weight of the Compound of the alpha-hydroxy acid, the at least one antiperspirant aluminum salt and optionally other ingredients is used.
  • the abovementioned amounts lead to a particularly good activation and stabilization of the antiperspirant aluminum salt even over longer storage periods.
  • the antiperspirant aluminum salt in a total amount of 1 to 99.99 wt .-%, preferably from 2 to 80 wt .-%, preferably from 3 to 60 wt .-%, more preferably from 4 to 50 wt .-%, in particular from 6 to 45 wt .-%, based on the total weight of the alpha-hydroxy acid, the at least one antiperspirant aluminum salt and optionally further ingredients is used.
  • a weight ratio of the antiperspirant aluminum salt to the alpha-hydroxy acid of 5,000: 1 to 1: 0.16, preferably from 1000: 1 to 1: 1, preferably from 100: 1 to 1: 5, more preferably from 50: 1 to 1:10, even more preferably from 10: 1 to 1:30, in particular from 4: 1 to 1: 50, is used.
  • the above-mentioned weight ratio refers to the total amount of all antiperspirant aluminum salts and all alpha-hydroxy acids in the antiperspirant cosmetic agent.
  • a total amount of free water is from 1 to 90% by weight, preferably from 5 to 80% by weight, preferably from 10 to 70% by weight, more preferably from 12 to 60% by weight. , in particular from 15 to 55 wt .-%, based on the total weight of the alpha-hydroxy acid, the at least one antiperspirant aluminum salt, the free water and optionally other ingredients is used.
  • the liquid mixture resulting from the activation and stabilization of the at least one antiperspirant aluminum salt by the alpha-hydroxy acid ⁇ can be carried out, for example, by means of conventional drying methods, such as spray drying.
  • the powders obtained in this way are excellent storage and have a long shelf life.
  • aqueous solutions are prepared and stored for 4 weeks at room temperature (in% by weight):
  • Such solutions are, inter alia, representative of hydrous antiperspirant emulsions (antiperspirant rollons, antiperspirant sticks, antiperspirant gels, antiperspirant pump sprayers).
  • the activation which results directly from the polymer distribution of the samples VI, E1 and E-II, is determined by size exclusion chromatography (also called “size exclusion chromatography" or SEC.)
  • size exclusion chromatography also called “size exclusion chromatography” or SEC.
  • SEC size exclusion chromatography
  • the respective sample is first adjusted to the concentration of 1 g ACH / 25 ml of water and filtered (0.2 ⁇ filter) .
  • the respective sample is then measured using SEC using a commercial HPLC equipment with a refractive index detector, using the following parameters:
  • peaks are obtained, with the lower retention time peaks for the ACH long chain polymers, and the higher retention time peaks for shorter chain length ACH polymers.
  • the peaks obtained for each sample in the chromatogram are integrated, with peaks 2 and 3 (long chain polymers), 4 to 8 (medium chain polymers), 9 to 1 1 (short chain polymers) and 12, and all subsequent peaks (very high) short chain length of the polymers) due to shoulders are integrated together.
  • the following table shows the area proportions of the peak groups 1, 2 to 3, 4 to 8, 9 to 1 1 and 12 and more in relation to the total area of the peaks obtained for the respective sample in the chromatogram:
  • E-Il 6 25 41 23 4 The formulations according to the invention El and E-Il have a significantly higher proportion of short-chain polymers (peaks 9 to 12 or more), ie, a significantly better activation and stabilization, than the Comparative Example VI. Consequently, the use of gluconic acid and glucone-5-lactone results in significantly improved activation and stabilization of the aluminum salt used.
  • the following formulation examples are intended to illustrate the subject matter of the invention without limiting it thereto.
  • the compounds of the formulas (HS-1), (HS-II) and / or (HS-III) used in the following examples are preferably salts of lactic acid (formula HS-1a), glucaric acid or salts thereof (formula HS-IIa ), Gluconic acid or its salts (formula HS-IIb), salts of lactobionic acid (formula HS-IIc), glucone-5-lactone (formula HS-I IIa) and mixtures thereof.
  • the compound of the formulas (HS-I) used in the following examples is preferably glycolic acid and salts thereof:
  • Antiperspirant cosmetic agents according to the invention (amounts in% by weight)
  • Cyclomethicone (at least 95% by weight cyclopentad ad ad ad siloxane) 100 100 100 100 100 100 100 100 100 100 100 100 Antiperspirant cosmetic agents according to the invention in the form of an oil-in-water emulsion (amounts in% by weight)
  • Antiperspirant cosmetic agents according to the invention in the form of microemulsions (in% by weight)
  • a single-layer substrate of 100% viscose having a weight per unit area of 50 g / m 2 was applied to 75 g each of the exemplary emulsions 14 or 15 per square meter or 75 g each of the exemplary compositions 10 and 11, respectively , cut into cloths of suitable size and packed in sachets.
  • Antiperspirant cosmetic agents according to the invention in the form of a water-in-oil emulsion (amounts in% by weight)
  • Antiperspirant cosmetic agents according to the invention (amounts in% by weight, based on the total weight of the blowing agent-free composition)
  • Example compositions 27-30 were filled into an aluminum epoxy spray can optionally coated with epoxy-phenolic lacquer in a weight ratio of propellant (butane / propane / isobutane mixture) to suspension of 80:20, 85:15, 60:40 and 90:10, respectively.
  • propellant butane / propane / isobutane mixture
  • Antiperspirant cosmetic agents according to the invention (amounts in% by weight, based on the total weight of the blowing agent-free composition)
  • Example compositions 31-33 were placed in an optionally epoxy-phenolic varnish-sprayed aluminum spray can at a weight ratio of propellant (butane / propane / isobutane mixture) to W / O emulsion of 80:20, 85:15, 60:40 and 90, respectively : 10 bottled.
  • propellant butane / propane / isobutane mixture
  • Antiperspirant cosmetic agents according to the invention in the form of O / W emulsions (amounts in parts by weight)
  • Antiperspirant cosmetic agents according to the invention (amounts in% by weight, based on the total weight of the blowing agent-free composition)
  • Example compositions 37-40 were placed in an optionally epoxy-phenolic lacquer sprayed aluminum spray can at a weight ratio of propellant (butane / propane / isobutane mixture) to W / O emulsion of 80:20, 85:15, 60:40, and 90, respectively : 10 bottled.
  • propellant butane / propane / isobutane mixture
  • Antiperspirant cosmetic compositions according to the invention in the form of W / O emulsions (amounts in% by weight)
  • Plantar ® 2000 DECYL GLUCOSIDE about 50% AS BASF

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Abstract

L'invention concerne un produit cosmétique anti-transpirant, contenant a) au moins une substance choisie dans le groupe constitué par les huiles cosmétiques qui sont à l'état liquide à une température de 20 °C et sous une pression de 1 013 h Pa, les parfums et les cires, b) au moins un sel d'aluminium anti-transpirant en quantité totale de 1 à 80 % en poids, rapportée au poids total du produit cosmétique anti-transpirant, et c) au moins un alpha-hydroxyacide particulier, l'ajout dudit au moins un alpha-hydroxyacide ayant pour conséquence une activation efficace dudit au moins un sel d'aluminium anti-transpirant et une excellente stabilisation de cet état activé.
EP14796688.1A 2013-10-15 2014-09-26 Produits cosmétiques anti-transpirants aux alpha-hydroxyacides Withdrawn EP3057567A2 (fr)

Applications Claiming Priority (2)

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DE201310220777 DE102013220777A1 (de) 2013-10-15 2013-10-15 Schweißhemmende kosmetische Mittel mit alpha-Hydroxysäuren
PCT/DE2014/200516 WO2015055199A2 (fr) 2013-10-15 2014-09-26 Produits cosmétiques anti-transpirants aux alpha-hydroxyacides

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DE102013220777A1 (de) 2015-04-16

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