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
  • A61K8/30—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
  • A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
  • A61K8/04—Dispersions; Emulsions
  • A61K8/06—Emulsions
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
  • A61K8/37—Esters of carboxylic acids
  • A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q19/00—Preparations for care of the skin

Definitions

• the invention relates to new emulsifier mixtures based on selected nonionic surfactants and their use for the production of PIT emulsions.
• the invention relates to emulsifier mixtures containing
• Fatty acid ethoxylates which are suitable as emulsifier component (a) preferably follow the formula (I)
• R 1 CO is a linear or branched acyl radical having 12 to 22 carbon atoms and n is a number from 5 to 50 and preferably 15 to 35.
• Typical examples are adducts of 20 to 30 moles of ethylene oxide with lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, elaeostearic acid, arachic acid, gadoleic acid and mixtures of erasic acid and behenic acid , which occur, for example, in the pressure splitting of natural fats and oils or in the reduction of aldehydes from Roelen's oxosynthesis.
• Addition products of 20 to 30 moles of ethylene oxide with fatty acids having 16 to 18 carbon atoms are preferably used.
• Partial glycerides which are suitable as emulsifier component (b) preferably follow the formula (II),
• R 2 CO stands for a linear or branched acyl radical with 12 to 22 carbon atoms and x, y and z in total for 0 or for numbers from 1 to 50, preferably 15 to 35.
• Typical examples of partial glycerides suitable for the purposes of the invention are lauric acid monoglyceride, coconut fatty acid monoglyceride, palmitic acid monoglyceride, stearic acid monoglyceride, isostearic acid monoglyceride, oleic acid monoglyceride and tallow fatty acid monoglyceride and their adducts with 5 to 50 and preferably 20 up to 30 moles of ethylene oxide.
• Monoglycerides or technical mono / diglyceride mixtures with a predominant monoglyceride content of the formula (II) are preferably used, in which R 2 CO represents a linear acyl radical having 16 to 18 carbon atoms.
• emulsifier mixtures which contain components (a) and (b) in a weight ratio of 10:90 to 90:10, preferably 25:75 to 75:25 and in particular 40:60 to 60:40.
• Another object of the invention therefore relates to the use of the emulsifier mixtures for the production of PIT emulsions, the mixtures generally being used in amounts of 1 to 10, preferably 3 to 8% by weight, based on the emulsions.
• Suitable oil bodies are, for example, Guerbet alcohols preferably containing 8 to 10 carbon atoms, esters of linear C ⁇ -C ⁇ come based on fatty alcohols having 6 to 18, o-fatty acids with linear C ⁇ -C ⁇ o fatty alcohols, esters of branched C6-Ci3-carboxylic acids with linear C6-C20-Fe.talkof.olen, esters of linear Ce-Ci ⁇ fatty acids with branched alcohols, in particular 2-ethylhexanol, esters of linear and / or branched fatty acids with polyhydric alcohols (such as dimer diol or trimer triol) and / or Guerbet alcohols, triglycerides based on Ce-Cio fatty acids, vegetable oils, branched primary alcohols, substituted cyclohexanes, Guerbet carbonates, dialkyl ethers and / or aliphatic or naphthenic hydrocarbons, which are usually used in amounts
• the PIT emulsions can be used for a large number of applications, but preferably for the production of skin and hair care products, such as, for example, hair shampoos, hair lotions, foam baths, creams, lotions or ointments. They can also be used as further auxiliaries and additives, surfactants, co-emulsifiers, superfatting agents, stabilizers, waxes, consistency agents, thickeners, cation polymers, silicone compounds, biogenic active ingredients, antidandruff agents, film formers, preservatives, hydrotropes, solubilizers, UV adsorbers, dyes and fragrances and the like included.
• skin and hair care products such as, for example, hair shampoos, hair lotions, foam baths, creams, lotions or ointments. They can also be used as further auxiliaries and additives, surfactants, co-emulsifiers, superfatting agents, stabilizers, waxes, consistency agents, thickeners, cation polymers,
• Suitable surfactants are fatty alcohol polyglycol ether sulfates, monoglyceride sulfates, mono- and / or dialkyl sulfosuccinates, fatty acid isethionates, fatty acid sarosinates, fatty acid taurides, ether carboxylic acids, alkyl oligoglucosides, fatty acid glucamides, alkyl amido betaines and / or preferably vegetable protein condensates.
• suitable co-emulsifiers are nonionic surfactants from at least one of the following groups:
• Castor oil (b5) polyol and especially polyglycerol esters such as e.g. Polyglycerol polyricinoleate or polyglycerol poly-12-hydroxystearate. Mixtures of compounds from several of these classes of substances are also suitable; (b6) adducts of 2 to 15 moles of ethylene oxide with castor oil and / or hardened castor oil; (b7) partial esters based on linear, branched, unsaturated or saturated Ci2 / 22 fatty acids,
• Ricinoleic acid and 12-hydroxystearic acid and glycerin polyglycerin, pentaerythritol, dipentaerythritol, sugar alcohols (e.g. sorbitol) and polyglucosides (e.g. cellulose); (b8) trialkyl phosphates; (b9) wool wax alcohols;
• adducts of ethylene oxide and / or of propylene oxide with fatty alcohols, alkylphenols, glycerol mono- and diesters as well as sorbitan mono- and diesters of fatty acids or with castor oil are known, commercially available products. These are mixtures of homologs, the average degree of alkoxylation of which is Ratio of the amounts of ethylene oxide and / or propylene oxide and substrate with which the addition reaction is carried out corresponds.
• C ⁇ / i ⁇ alkyl mono- and oligoglycosides their preparation and their use as surface-active substances are, for example, from US 3,839,318, US 3,707,535, US 3,547,828, DE-OS 19 43 689, DE-OS 20 36 472 and DE-A1 30 01 064 and EP-A 0 077 167 are known. They are produced in particular by reacting glucose or oligosaccharides with primary alcohols with 8 to 18 carbon atoms.
• the glycoside residue both monoglycosides in which a cyclic sugar residue is glycosidically bonded to the fatty alcohol and oligomeric glycosides with a degree of oligomerization of up to approximately 8 are suitable.
• the degree of oligomerization is a statistical mean value which is based on a homolog distribution customary for such technical products.
• Zwitterionic surfactants can also be used as emulsifiers.
• Zwitterionic surfactants are surface-active compounds that contain at least one quaternary ammonium group and at least one carboxylate and one sulfonate group in the molecule.
• Particularly suitable zwitterionic surfactants are the so-called betaines such as the N-alkyl-N, N-dimethylammonium glycinate, for example the coconut alkyldimethylammonium glycinate, N-acylaminopropyl-N, N-dimethylammonium glycinate, for example the coconut acylaminopropyldimethylammonium glycinate, and 2-alkyl-3-carboxylate -3-hydroxyethylimidazolines each having 8 to 18 carbon atoms in the alkyl or acyl group and the cocoacylaminoethylhydroxyethylcarboxymethylglycinate.
• betaines such as the N-alkyl-N, N-dimethylammonium glycinate, for example the coconut alkyldimethylammonium glycinate, N-acylaminopropyl-N, N-dimethylammonium glycinate
• Suitable emulsifiers are ampholytic surfactants.
• Ampholytic surfactants are surface-active compounds which, in addition to a C ⁇ / i ⁇ alkyl or acyl group, contain at least one free amino group and at least one -COOH or -S ⁇ 3H group in the molecule and are capable of forming internal salts.
• ampholytic surfactants are N-alkylglycine, N-alkylpropionic acid, N-alkylaminobutyric acid, N-alkyliminodipropionic acid, N-hydroxyethyl-N-alkylamidopropylglycine, N-alkyltaurine, N-alkyl sarcosine, 2-alkylaminopropionic acid and alkylaminoacetic acid each with about 8 to 18 C. Atoms in the alkyl group.
• Particularly preferred ampholytic surfactants are N-cocoalkylaminopropionate, cocoacylaminoethyl aminopropionate and Cizn ⁇ -acylsarcosine.
• quaternary emulsifiers are also suitable, those of the esterquat type, preferably methyl-quaternized difatty acid triethanolamine ester salts, being particularly preferred.
• Substances such as, for example, lanolin and lecithin and polyethoxylated or acylated lanolin and lecithin derivatives, polyol fatty acid esters and fatty acid alkanolamides can be used as superfatting agents, the latter simultaneously serving as foam stabilizers.
• As consistency agents primarily fatty alcohols with 12 to 22 and preferably 16 to 18 carbon atoms come into consideration. A combination of these substances with alkyl oligoglucosides and / or fatty acid N-methyl-glucamides of the same chain length and / or polyglycerol poly-12-hydroxy stearates is preferred.
• Suitable thickeners are, for example, polysaccharides, in particular xanthan gum, guar guar, agar agar, alginates and tyloses, carboxymethyl cellulose and hydroxyethyl cellulose, furthermore higher molecular weight polyethylene glycol mono- and diesters of fatty acids, polyacrylates, polyvinyl alcohol and polyvinylpyrrolidone, surfactants such as, for example, ethoxylated fatty acid glycerides, esters of fatty acids with polyols such as, for example, pentaerythritol or trimethylolpropane, fatty alcohol ethoxylates with a narrowed homolog distribution or alkyl oligoglucochloride as well as ammonium oligoglium chloride.
• polysaccharides in particular xanthan gum, guar guar, agar agar, alginates and tyloses, carboxymethyl cellulose and
• Suitable cationic polymers are, for example, cationic cellulose derivatives, cationic starch, copolymers of diallylammonium salts and acrylamides, quaternized vinylpyrrolidone / vinylimidazole polymers such as e.g. Luviquat® (BASF AG, Ludwigshafen / FRG), condensation products of polyglycols and amines, quaternized collagen polypeptides such as lauryldimonium hydroxypropyl hydrolyzed collagen (Lamequat®L, Grünau GmbH), quaternized wheat polypeptides, polyethyleneimine, cationic silicone polymers such as e.g.
• Cartaretine®, Sandoz CH polya
• Suitable silicon compounds are, for example, dimethylpolysiloxanes, methylphenylpolysiloxanes, cyclic silicones and amino-, fatty acid-, alcohol-, polyether-, epoxy-, fluorine- and / or alkyl-modified silicone compounds, which can be both liquid and resinous at room temperature.
• Typical examples of fats are glycerides; beeswax, paraffin wax or microwaxes may be used as waxes, if appropriate in combination with hydrophilic waxes, for example cetylstearyl alcohol.
• Pearlescent waxes which can be used are, in particular, mono- and difatty acid esters of polyalkylene glycols, partial glycerides or esters of fatty alcohols with polybasic carboxylic acids or hydroxycarboxylic acids.
• Metal salts of fatty acids such as magnesium, aluminum and / or zinc stearate can be used as stabilizers.
• Biogenic active substances are understood to mean, for example, bisabolol, allantoin, phytantriol, panthenol, AHA acids, plant extracts and vitamin complexes.
• Climbazoi, octopirox and zinc pyrethione can be used as antidandruff agents.
• Common film formers are, for example, chitosan, microcrystalline chitosan, quaternized chitosan, polyvinylpyrrolidone, vinylpyrrolidone-vinyl acetate copolymers, polymers of the acrylic acid series, quaternary cellulose derivatives, collagen, hyaluronic acid or its salts and similar compounds.
• Hydrotropes such as ethanol, isopropyl alcohol, propylene glycol or glucose can also be used to improve the flow behavior.
• Suitable preservatives are, for example, phenoxyethanol, formaldehyde solution, parabens, pentanediol or sorbic acid.
• Suitable dyes are those which are suitable and approved for cosmetic purposes Substances are used, as compiled, for example, in the publication "Cosmetic Colorants” by the Dye Commission of the German Research Foundation, Verlag Chemie, Weinheim, 1984, pp. 81-106. These dyes are usually used in concentrations of 0.001 to 0.1% by weight, based on the mixture as a whole.
• the total proportion of auxiliaries and additives can be 1 to 50, preferably 5 to 40% by weight, based on the emulsions.

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• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Veterinary Medicine (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Birds (AREA)
• Epidemiology (AREA)
• Emergency Medicine (AREA)
• Dispersion Chemistry (AREA)
• Chemical & Material Sciences (AREA)
• Dermatology (AREA)
• Cosmetics (AREA)
• Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
• Colloid Chemistry (AREA)

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• 1996
  • 1996-09-02 DE DE19635553A patent/DE19635553A1/de not_active Ceased
• 1997
  • 1997-08-25 US US09/254,029 patent/US6221370B1/en not_active Expired - Lifetime
  • 1997-08-25 ES ES97919000T patent/ES2210517T5/es not_active Expired - Lifetime
  • 1997-08-25 WO PCT/EP1997/004621 patent/WO1998009721A2/de not_active Ceased
  • 1997-08-25 JP JP10512188A patent/JP2001500424A/ja not_active Ceased
  • 1997-08-25 EP EP97919000A patent/EP0938369B2/de not_active Expired - Lifetime
  • 1997-08-25 DE DE59711006T patent/DE59711006D1/de not_active Expired - Lifetime

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