EP1478336A1 - Preparation pour parfum comprenant du 2- methyl-1, 3- propandiol - Google Patents

Preparation pour parfum comprenant du 2- methyl-1, 3- propandiol

Info

Publication number
EP1478336A1
EP1478336A1 EP03708084A EP03708084A EP1478336A1 EP 1478336 A1 EP1478336 A1 EP 1478336A1 EP 03708084 A EP03708084 A EP 03708084A EP 03708084 A EP03708084 A EP 03708084A EP 1478336 A1 EP1478336 A1 EP 1478336A1
Authority
EP
European Patent Office
Prior art keywords
aqueous
dermatological
methyl
cosmetic
propanediol
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Withdrawn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
EP03708084A
Other languages
German (de)
English (en)
Inventor
Rainer Kröpke
Jens Nielsen
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.)
Beiersdorf AG
Original Assignee
Beiersdorf AG
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 Beiersdorf AG filed Critical Beiersdorf AG
Publication of EP1478336A1 publication Critical patent/EP1478336A1/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Withdrawn legal-status Critical Current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
    • A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • 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
    • A61K8/34—Alcohols
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q13/00—Formulations or additives for perfume preparations

Definitions

  • the present invention relates to aqueous and / or alcoholic cosmetic and / or dermatological preparations containing 2-methyl-1, 3-propanediol and perfume oil with a difference in the refractive index of the dispersed phase and the outer phase of greater than 0.003, the process for the preparation and their use.
  • Fragrances and perfumes have been used by people to influence their environment since time immemorial. It can be assumed that a multitude of natural fragrance sources already existed in the environment of early humans, which he also used in connection with the satisfaction of primitive needs. With the discovery of fire, the use of fragrances received strong impulses and a new dimension in human life. The smoke offering is the oldest form of worshiping the gods, and the burning of certain parts of plants is one of the oldest methods of producing fragrance. The fragrance unfolds "per fumum" through the smoke.
  • perfumes are made from natural plant and animal fragrances and from chemically synthesized compounds.
  • Herbal fragrances are usually obtained by steam distillation in the form of essential oils.
  • One example is the eugenol obtained from clove oil.
  • volatile, temperature-sensitive fragrances for example the oil from jasmine flowers, enfleurage has been used since ancient times as an extraction process to obtain the "Absolu de Chassis".
  • Sensitive citrus oils are obtained by squeezing fruit peels. for example for the production of resinoids from balsams and resins or benzoin from certain types of lichen and moss, use.
  • Animal fragrances are mainly obtained from glandular excretions of certain animal species such as musk, civet or beaver. Due to their strong smell, these glandular secretions, which are mainly used by animals to mark territory, are only used in diluted form.
  • Fragrances and the perfume oils made from them are used in almost all cosmetic preparations as well as in detergents and household cleaners. They serve to mask the intrinsic odor of components of these preparations and, in the case of cosmetics and detergents, the intrinsic odor of their users [W. Umbach (ed.): Cosmetics, development, manufacture and application of cosmetic products, 2nd edition, Thieme Verlag, Stuttgart, 1995].
  • Fragrances and the perfume oils made from them are mostly non-polar, oil-soluble compounds and mixtures that are difficult or not soluble in water, alcohol or aqueous-alcoholic solutions.
  • these solubilizers are added. These usually have an amphiphilic structure and are similar to emulsifiers and tesides.
  • ethoxylated carbohydrates or fatty acid derivatives for example polyoxyethylene (20) sorbitan monolaurate (Tween 20) or polyoxyethylene oxypropylene monostearate (Atlas G-2162), are used to impart perfume oils.
  • solubilizers in cosmetic or dermatological preparations are harmless. Nevertheless, solubilizers, like ultimately every chemical substance, can cause allergic or hypersensitive reactions in individual cases. Skin irritation, for example, can occur as an undesirable side effect in sensitive people. Therefore their concentration in cosmetic or dermatological preparations should be kept as low as possible or avoided entirely.
  • solubilizers are also a disadvantage of the prior art that complex mixtures of solubilizers often have to be used in order to achieve stable cosmetic preparations.
  • the suitable compositions of these mixtures can usually only be found out by trial and error, which makes the development of these preparations lengthy and expensive.
  • solubilizers are not pure substances but, due to the manufacturing process, mixtures, which further increases the problems with product compatibility and product stability.
  • aqueous and / or alcoholic cosmetic preparations are transparent. However, consumers often associate water-clear, transparent solutions with products with a low active ingredient content. Slightly cloudy products, on the other hand, are associated with a high active ingredient content and high cosmetic or dermatological performance.
  • aqueous and / or alcoholic cosmetic and / or dermatological preparations containing a) 2-methyl-1,3-propanediol in a concentration of 0.5 to 30% by weight, b) perfume oil in a concentration of 0 , 01 to 10.0% by weight, based in each case on the total weight of the preparation, with a difference in the refractive indices of the dispersed phase and the outer phase of greater than 0.003.
  • These preparations are characterized by a high tolerance and care performance. They can also be used to easily formulate a large number of extremely stable cosmetic and / or dermatological preparations.
  • the preparations according to the invention a) 2-methyl-1,3-propanediol in a concentration of 2 to 10% by weight, b) perfume oil in a concentration of 0.1 to 3.0% by weight, in each case based on the total weight of the preparation included.
  • the difference in the refractive indices of the dispersed phase and the outer phase is greater than 0.01.
  • the weight ratio of 2-methyl-1,3-propanediol to perfume oil in the preparations according to the invention is advantageously from 1: 1 to 100: 1 and particularly preferably from 5: 1 to 50: 1.
  • the alcohol which is particularly preferred according to the invention is ethanol.
  • the aqueous and / or alcoholic cosmetic and / or dermatological preparations according to the invention can, depending on the application, contain further cosmetic and / or dermatological active ingredients, auxiliaries and / or additives.
  • the use of the preparations according to the invention for purposes other than cosmetic or dermatological purposes, for example as detergents, cleaning agents, household cleaners or disinfectants, is also in accordance with the invention in the compositions customary for these compositions, the list of these uses being in no way intended to be limiting.
  • an aqueous solution according to the invention can also contain other ingredients according to the invention, for example alcohols, diols or polyols of low C number, and their ethers, preferably ethanol, isopropanol, propylene glycol, glycerol, ethylene glycol, ethylene glycol monoethyl or monobutyl ether, propylene glycol monomethyl, monoethyl or monobutyl ether, diethylene glycol monomethyl or monoethyl ether and similar products, furthermore alcohols with a low C number, for example ethanol, isopropanol, 1, 2-propanediol and glycerol.
  • alcohols, diols or polyols of low C number, and their ethers preferably ethanol, isopropanol, propylene glycol, glycerol, ethylene glycol, ethylene glycol monoethyl or monobutyl ether, propylene glycol monomethyl, monoethyl or mono
  • the preparations according to the invention can advantageously contain thickeners.
  • These thickeners can advantageously be selected from the group of gums, polysaccharides, cellulose derivatives, layered silicates, polyacrylates and / or other polymers.
  • Gums include plant or tree sap that harden in the air and form resins or extracts from aquatic plants. Gum arabic, locust bean gum, tragacanth, karaya, guar gum, pectin, gellan gum, carrageenan, agar, algine, chondrus, xanthan gum can advantageously be selected from this group for the purposes of the present invention.
  • derivatized gums such as e.g. Hydroxy-propyl guar (Jaguar® HP 8).
  • polysaccharides and derivatives are e.g. Hyaluronic acid, chitin and chitosan, chondroitin sulfates, starch and starch derivatives.
  • cellulose derivatives are e.g. Methyl cellulose, carboxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl methyl cellulose.
  • Layered silicates contain naturally occurring and synthetic clays such as Montmorillonite, bentonite, hectorite, laponite, magnesium aluminum silicates such as Veegum®. These can be used as such or in a modified form such as e.g. Stearylalkonium hektorite.
  • silica gels can also advantageously be used.
  • the polymers according to the invention include, for example, polyacrylamides (Seppigel 305), polyvinyl alcohols, PVP, PVP / VA copolymers, polyglycols.
  • Polyacrylates which are advantageous according to the invention are polymers of acrylic acid, in particular those selected from the group of the so-called carbomers or carbopols (Carbopol® is actually a registered trademark of the Noveon Company). Polyacrylates are compounds of the general structural formula
  • the group of polyacrylates also includes acrylate-alkyl acrylate copolymers, for example those which are distinguished by the following structure:
  • R ' represents a long-chain alkyl radical and x and y numbers which symbolize the respective stoichiometric proportion of the respective comonomers.
  • Examples of advantageous carbopoles are types 907, 910, 934, 940, 941, 951, 954, 980, 981, 1342, 1382, 2984 and 5984 or types ETD (Easy-to-disperse) 2001, 2020, 2050, where these compounds can be present individually or in any combination with one another.
  • Carbopol 981, 1382 and ETD 2020 are particularly preferred.
  • the alkyl acrylate to acrylate copolymers, copolymers of comparable C 10-3 o-alkyl acrylates and one or more monomers of acrylic acid, methacrylic acid or esters thereof are "Acrylates / C 10-30 Alkyl Acrylate Crosspolymer".
  • Particularly advantageous are those available under the trade names Pemulen TR1 and Pemulen TR2 from the BF Goodrich Company.
  • Terpolymers for example made from vinylpyrrolidone, dimethylaminopropyl methacrylamide and quaternized alkyldimethylaminopropyl methacrylamide, can also be used advantageously according to the invention.
  • compositions optionally contain the additives customary in cosmetics, for example perfume, dyes, antimicrobial substances, refatting agents, complexing and sequestering agents, pearlescent agents, further plant extracts, vitamins, active ingredients, preservatives, bactericides, self-tanning agents , Depigmenting agents, pigments that have a coloring effect, softening, moisturizing and / or moisturizing substances, or other customary components of a cosmetic or dermatological formulation such as polymers, foam stabilizers, electrolytes, organic solvents or silicone derivatives.
  • additives customary in cosmetics for example perfume, dyes, antimicrobial substances, refatting agents, complexing and sequestering agents, pearlescent agents, further plant extracts, vitamins, active ingredients, preservatives, bactericides, self-tanning agents , Depigmenting agents, pigments that have a coloring effect, softening, moisturizing and / or moisturizing substances, or other customary components of a cosmetic or dermatological formulation such as polymers,
  • antioxidants are generally preferred. According to the invention, all the antioxidants suitable or customary for cosmetic and / or dermatological applications can be used as favorable antioxidants.
  • the preparations according to the invention can advantageously contain small amounts of preservatives approved for food.
  • Preservatives approved in food technology which can also be used advantageously for the purposes of the present invention, are listed below with their E number.
  • preservatives or preservatives such as dibromodicyanobutane (2-bromo-2-bromomethylglutarodinitrile), phenoxyethanol, 3-iodo-2-propynylbutylcarbamate, 2-bromo-2-nitro-propane-1, 3-diol , Imidazolidinyl urea, 5-chloro-2-methyl-4-isothiazolin-3-one, 2-chloroacetamide, benzalkonium chloride, benzyl alcohol.
  • dibromodicyanobutane (2-bromo-2-bromomethylglutarodinitrile)
  • phenoxyethanol 3-iodo-2-propynylbutylcarbamate
  • 2-bromo-2-nitro-propane-1 3-diol
  • Imidazolidinyl urea 5-chloro-2-methyl-4-isothiazolin-3-one
  • 2-chloroacetamide benzalkonium chloride
  • the preparations according to the invention can advantageously contain one or more wash-active anionic, cationic, amphoteric and / or non-ionic surfactants. It is particularly advantageous to choose the wash-active surfactant or surfactants according to the invention from the group of surfactants which have an HLB value of more than 25, very particularly advantageous are those which have an HLB value of more than 35.
  • acylglutamates especially sodium acylglutamate
  • ⁇ sarcosinates for example myristoyl sarcosine, TEA-lauroyl sarcosinate, sodium and sodium,
  • acyl isethionates eg sodium / Ammoniumcocoyl isethionate
  • Sulfosuccinates for example dioctyl sodium sulfosuccinate, disodium laureth sulfosuccinate, disodium lauryl sulfosuccinate and disodium undecylenamido MEA sulfosuccinate
  • sulfuric acid esters such as
  • Alkyl ether sulfate for example sodium, ammonium, magnesium, MIPA, TIPA laureth sulfate, sodium myreth sulfate and sodium C 12 . 13 pareth sulfate,
  • Alkyl sulfates for example sodium, ammonium and TEA lauryl sulfate.
  • Quaternary surfactants are particularly advantageous washing-active cationic surfactants for the purposes of the present invention.
  • Quaternary surfactants contain at least one N atom which is covalently linked to 4 alkyl or aryl groups. Benzalkonium chloride, alkyl betaine, alkyl amidopropyl betaine and alkyl amidopropyl hydroxysultain are advantageous.
  • acyl / dialkylethylenediamines for example sodium, Dinatriumacyl- amphodipropionat, disodium, Natriumacylamphohydroxypropyl- sulfonate, and sodium acyl Dinatriumacylamphodiacetat,
  • alkanolamides such as cocamides MEA DEA / MIPA, ⁇ esters formed by esterification of carboxylic acids with ethylene oxide, glycerol, sorbitan or other alcohols,
  • ⁇ ethers for example ethoxylated alcohols, ethoxylated lanolin, ethoxylated polysiloxanes, propoxylated POE ethers and alkyl polyglycosides such as lauryl glucoside, decyl glycoside and cocoglycoside.
  • ⁇ taurates for example sodium lauroyl taurate and sodium methyl cocoyl taurate
  • ⁇ ether carboxylic acids for example sodium laureth-13 carboxylate and sodium PEG-6 cocamide carboxylate, Phosphoric acid esters and salts, such as DEA-Oleth-10 phosphate and dilaureth-4 phosphate,
  • Alkyl sulfonates for example sodium coconut monoglyceride sulfate, sodium C 12- , 4 olefin sulfonate, sodium lauryl sulfoacetate and magnesium PEG-3 cocamide sulfate.
  • N-alkylamino acids for example aminopropylalkylglutamide, alkylaminopropionic acid, sodium alkylimidodipropionate and lauroamphocarboxyglycinate.
  • non-ionic surfactants are alcohols.
  • glutamates such as di-TEA-palmitoyl aspartate and sodium caprylic / capric glutamate,
  • carboxylic acids and derivatives such as
  • ⁇ for example lauric acid, cylenat aluminum stearate, magnesium and Zinisme-, ⁇ ester carboxylic acids, for example calcium stearoyl lactylate, laureth-6 citrate and sodium PEG-4 lauramide carboxylate,
  • Suitable cationic surfactants for the purposes of the present invention are also ⁇ alkylamines,
  • Suitable nonionic surfactants for the purposes of the present invention are also amine oxides, such as cocoamidopropylamine oxide.
  • Preparations in the sense of the present invention can preferably contain at least one UV-A, UV-B and / or broadband filter substance
  • Advantageous UV filter substances for the purposes of the present invention are, for example, sulfonated, water-soluble UV filters, such as:
  • Salts (especially the corresponding 10-sulfato compounds, especially the corresponding sodium, potassium or triethanolammonium salt), which is also referred to as benzene-1, 4-di (2-oxo-3-bornylidenemethyl-10-sulfonic acid) , Benzene-1,4-di (2-oxo-3-bomylidenemethyl-10-sulfonic acid) has the INCI name Terephthalic Dicampher Sulfonic Acid (CAS No. 90457-82-2) and is, for example, under the trade name Mexoryl SX available from Chimex; Sulfonic acid derivatives of 3-benzylidene camphor, such as.
  • the preparations according to the invention advantageously contain the substances which absorb UV radiation in the UV-A and / or UV-B range in a total amount of, for. B. 0.1% by weight to 30% by weight, preferably 0.5 to 20% by weight, in particular 1.0 to 15.0% by weight, in each case based on the total weight of the emulsions, for cosmetic purposes To provide preparations that protect the hair or skin from the entire range of ultraviolet radiation.
  • large amounts of acidic aluminum and / or aluminum / zirconium salts can advantageously be incorporated stably into the preparation.
  • 5 to 40% by weight, in particular 10 to 20% by weight, aluminum chlorohydrate and / or aluminum / zirconium chlorohydrate can be stably incorporated into the preparations according to the invention.
  • the concentration ranges described here relate to the so-called active contents of the antiperspirant complexes: for the aluminum compounds to anhydrous complexes, for the aluminum / zirconium compounds to anhydrous and buffer-free complexes.
  • Glycine is usually used here as a buffer.
  • Aluminum salts such as aluminum chloride AICI 3 , aluminum sulfate AI 2 (S0) 3
  • Standard AI complexes Aluminum Sesquichlorohydrate (Reheis), ACH-308 (Summit), Aloxicoll 31 L (Giulini)
  • Aluminum-zirconium salts • Aluminum / zirconium trichlorohydrex glycine [AI 4 Zr (OH) 13 CI 3 ] x H 2 O x Gly
  • L435G (Giulini) Activated Al / Zr complexes: Reach AZP 855 (Reheis), AAZG-6313-15 (Summit), Zirkonal AP4G (Giulini)
  • glycine-free aluminum / zirconium salts can also be advantageous.
  • antiperspirants from the raw material classes aluminum and aluminum / zirconium salts should not affect the commercially available, mostly aqueous solutions, e.g. Locron L (Clahant), may be limited, but it may also be advantageous to use the commercially available anhydrous powders of the same raw materials by incorporating them into the claimed formulations, such as Locron P (Clariant).
  • antiperspirants are based on other metals, such as e.g. aluminum or zirconium. Beryllium, titanium, hafnium.
  • antiperspirant active ingredients should not be limited to metal-containing raw materials, but also compounds that contain non-metals such as boron and those that belong to the field of organic chemistry, such as e.g. Anticholinergics.
  • polymers which can be both metal-containing and metal-free are also advantageous.
  • the method for producing an aqueous and / or alcoholic cosmetic and / or dermatological preparation according to the invention is also according to the invention. This is characterized in that the perfume oil is first dissolved in 2-methyl-1,3-propanediol and then the remaining components of the preparation are added.
  • aqueous and / or alcoholic cosmetic and / or dermatological preparations as a facial tonic, fragrant water, aftershave, deodorant, antiperspirant, facial cleansing water, make-up remover, hair tonic, hair fixer and hair styling agent, bath additive, foam or shower bath is also in accordance with the invention. repellent, depigmenting agent.
  • aqueous and / or alcoholic cosmetic and / or dermatological preparations according to one of the preceding claims as water, solution, impregnation, tincture or spray is also according to the invention.
  • Aqueous and / or alcoholic preparation Aqueous and / or alcoholic preparation

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Cosmetics (AREA)
  • Detergent Compositions (AREA)

Abstract

L'invention concerne une préparation cosmétique et/ou dermatologique, aqueuse et/ou alcoolique, contenant a) du 2-méthyl-1,3-propandiol dans une concentration de 0,5 à 10 % en poids, b) de l'huile essentielle dans une concentration de 0,01 à 10,0 % en poids, ces concentrations se rapportant au poids total de la préparation, la différence des indices de réfraction de la phase en dispersion et de la phase externe étant supérieure à 0,003.
EP03708084A 2002-02-08 2003-02-07 Preparation pour parfum comprenant du 2- methyl-1, 3- propandiol Withdrawn EP1478336A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE10205192 2002-02-08
DE10205192A DE10205192A1 (de) 2002-02-08 2002-02-08 Diolhaltige Parfümkomposition
PCT/EP2003/001203 WO2003066011A1 (fr) 2002-02-08 2003-02-07 Préparation pour parfum comprenant du 2- méthyl-1, 3- propandiol

Publications (1)

Publication Number Publication Date
EP1478336A1 true EP1478336A1 (fr) 2004-11-24

Family

ID=27618438

Family Applications (1)

Application Number Title Priority Date Filing Date
EP03708084A Withdrawn EP1478336A1 (fr) 2002-02-08 2003-02-07 Preparation pour parfum comprenant du 2- methyl-1, 3- propandiol

Country Status (5)

Country Link
US (1) US20050064000A1 (fr)
EP (1) EP1478336A1 (fr)
JP (1) JP2005517692A (fr)
DE (1) DE10205192A1 (fr)
WO (1) WO2003066011A1 (fr)

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Also Published As

Publication number Publication date
DE10205192A1 (de) 2003-08-21
US20050064000A1 (en) 2005-03-24
WO2003066011A1 (fr) 2003-08-14
JP2005517692A (ja) 2005-06-16

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