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IPC classes for russian patent Hair care compositions (RU 2424791):
Hair straightening composition containing urea / 2424790
Invention relates to cosmetology, specifically to a water-based hair straightening composition, having pH between 12 and 14, containing i) a hydroxide ion generator selected from a group comprising lithium hydroxide, potassium hydroxide, guanidine hydroxide and sodium hydroxide; and ii) 0.5-20 wt % urea, where the weight ratio of urea to the hydroxide ion generator is between 12:1 and 3:1. The invention also relates to a method for lanthionisation of keratin fibre.
Antiperspirant and deodorant compositions / 2424789
Invention relates to field of cosmetics. Water-free antiperspirant or deodorant composition, which contains: particle of astringent antiperspirant salt; 20-90 wt % of oil-carrier, gelling agent for oil-carrier and moisturiser-polyol, moisturiser-polyol constituting 0.1-10% in terms of composition weight, polyethylene glycol has average molecular weight to 820. Product, containing composition is in distributing vessel, which contains balloon, on one end of which there is at least one hole, through which composition can be pushed out, and on the opposite, second end there is lift, fitting internal surface of balloon and able to move to the first end. Non-therapeutic method of suppressing sweating or weakening body smell, including stage of topic application of composition on skin.
Antimicrobial and anti-inflammatory substances, isolated from licorice extract / 2423116
Invention relates to pharmaceutical industry, in particular, to antibacterial and anti-inflammatory composition. Antibacterial or anti-inflammatory composition for oral cavity or body care, including extract from roots of plant Glycyrrhiza sp., main components of extract being prenylated flavonoids, and roots are extracted by method of CO2 extracting in supercritical state.
Fragrances with reduced content of sulphur and their application in compositions for oral cavity care / 2423102
Invention relates to cosmetic industry, in particular to composition for oral cavity care. Product for oral cavity care, containing agent for oral cavity care, which possesses chemical reducing ability, taste system, containing fragrance(s) or extract(s), in fact free of sulphur-containing compounds, which include dimethyl sulfoxide, dimethyl sulfide, dimethyl disulfide and dimethyl sulfone, which are precursors of formation of unpleasant smell and taste sensations, and suitable for introduction into oral cavity, agent for oral cavity care being selected from source of tin(2) ions and phenol resins from sources selected from tea, cranberry, pomegranate and oak bark.
Pyperidinium compounds and cosmetic compositions containing them / 2423101
Invention relates to field of cosmetology, in particular, deals with compound, called 4-[(2-cyclopentyl-2-hydroxyphenylacetyl)oxy]-1,1-dimethylpyperidinium bromide, which has formula: and compound, called 4-[(2-cyclohexyl-2-hydroxyphenylacetyl)oxy]-1,1-dimethylpyperidinium bromide, which has formula: , as well as describes cosmetic and dermatological compositions, containing them, and method of reduction or inhibition of perspiration by them.
Therapeutic-preventive composition for teeth and oral cavity care / 2423100
Invention relates to field of dentistry, namely, to compositions for teeth and oral cavity care. Therapeutic-preventive composition contains sodium fluoride, sodium lauryl sulfate, lauryl glucosi, cocamidopropyl betaine, polyvinylpyrrolidone, panthenol, phytopain, propolis extract, saccharin, fragrance and water with definite component ratio.
Mousse for oral cavity care / 2423099
Invention relates to preparations for oral cavity care. Mousse includes composition of preparation for teeth cleaning, which consists of surfactant, moisturiser, fragrance, binding and pharmaceutical agents, and liquid propellant, which consists of mixture of isobutene and propane in definite ratio. Mousse has viscosity from 5000 to less than 30000 santipoise (mps) at definite temperature before propellant addition. Dispersed as gel, mousse lathers and increases in volume, at least, by 100 vol % for less than 5 seconds at atmospheric pressure.
Method of obtaining biologically active sybstance from sturgeon for cosmetic products (versions) / 2422131
Invention relates to cosmetic industry, namely to method of obtaining biologically active substance from sturgeon for cosmetic products. Method includes antemortem taking of roe, separation from roe by decantation of roe sol, purification of the latter through filter with pore diameter 0.02-0.10 mm, homogenisation at rotation speed 45-65 rev/sec for 4-15 min, and preservation by homogenate pasteurisation or ultrasound processing. In accordance with second version method includes antemortem taking of roe, separation of roe sol from roe by decantation, purification of the latter through filter with cell width or pore diameter 0.02-0.10 mm, homogenisation at rotation rate 45-65 rev/sec for 4-15 minutes, preservation, drying on dispersion drier at air temperature at input of drying chamber plus 140°C, at output - plus 80°C, with frequency of disperser rotation 25 thousand rev/min or drying on sublimation drier at temperature minus 35-40°C with further additional drying at temperature plus 30°C.
Method of obtaining biologically active sybstance from sturgeon for cosmetic products (versions) / 2422131
Invention relates to cosmetic industry, namely to method of obtaining biologically active substance from sturgeon for cosmetic products. Method includes antemortem taking of roe, separation from roe by decantation of roe sol, purification of the latter through filter with pore diameter 0.02-0.10 mm, homogenisation at rotation speed 45-65 rev/sec for 4-15 min, and preservation by homogenate pasteurisation or ultrasound processing. In accordance with second version method includes antemortem taking of roe, separation of roe sol from roe by decantation, purification of the latter through filter with cell width or pore diameter 0.02-0.10 mm, homogenisation at rotation rate 45-65 rev/sec for 4-15 minutes, preservation, drying on dispersion drier at air temperature at input of drying chamber plus 140°C, at output - plus 80°C, with frequency of disperser rotation 25 thousand rev/min or drying on sublimation drier at temperature minus 35-40°C with further additional drying at temperature plus 30°C.
Method of obtaining biologically active sybstance from sturgeon for cosmetic products (versions) / 2422131
Invention relates to cosmetic industry, namely to method of obtaining biologically active substance from sturgeon for cosmetic products. Method includes antemortem taking of roe, separation from roe by decantation of roe sol, purification of the latter through filter with pore diameter 0.02-0.10 mm, homogenisation at rotation speed 45-65 rev/sec for 4-15 min, and preservation by homogenate pasteurisation or ultrasound processing. In accordance with second version method includes antemortem taking of roe, separation of roe sol from roe by decantation, purification of the latter through filter with cell width or pore diameter 0.02-0.10 mm, homogenisation at rotation rate 45-65 rev/sec for 4-15 minutes, preservation, drying on dispersion drier at air temperature at input of drying chamber plus 140°C, at output - plus 80°C, with frequency of disperser rotation 25 thousand rev/min or drying on sublimation drier at temperature minus 35-40°C with further additional drying at temperature plus 30°C.
Hair straightening composition containing urea / 2424790
Invention relates to cosmetology, specifically to a water-based hair straightening composition, having pH between 12 and 14, containing i) a hydroxide ion generator selected from a group comprising lithium hydroxide, potassium hydroxide, guanidine hydroxide and sodium hydroxide; and ii) 0.5-20 wt % urea, where the weight ratio of urea to the hydroxide ion generator is between 12:1 and 3:1. The invention also relates to a method for lanthionisation of keratin fibre.
Hair straightening composition containing urea / 2424790
Invention relates to cosmetology, specifically to a water-based hair straightening composition, having pH between 12 and 14, containing i) a hydroxide ion generator selected from a group comprising lithium hydroxide, potassium hydroxide, guanidine hydroxide and sodium hydroxide; and ii) 0.5-20 wt % urea, where the weight ratio of urea to the hydroxide ion generator is between 12:1 and 3:1. The invention also relates to a method for lanthionisation of keratin fibre.
Antiperspirant and deodorant compositions / 2424789
Invention relates to field of cosmetics. Water-free antiperspirant or deodorant composition, which contains: particle of astringent antiperspirant salt; 20-90 wt % of oil-carrier, gelling agent for oil-carrier and moisturiser-polyol, moisturiser-polyol constituting 0.1-10% in terms of composition weight, polyethylene glycol has average molecular weight to 820. Product, containing composition is in distributing vessel, which contains balloon, on one end of which there is at least one hole, through which composition can be pushed out, and on the opposite, second end there is lift, fitting internal surface of balloon and able to move to the first end. Non-therapeutic method of suppressing sweating or weakening body smell, including stage of topic application of composition on skin.
Antiperspirant and deodorant compositions / 2424789
Invention relates to field of cosmetics. Water-free antiperspirant or deodorant composition, which contains: particle of astringent antiperspirant salt; 20-90 wt % of oil-carrier, gelling agent for oil-carrier and moisturiser-polyol, moisturiser-polyol constituting 0.1-10% in terms of composition weight, polyethylene glycol has average molecular weight to 820. Product, containing composition is in distributing vessel, which contains balloon, on one end of which there is at least one hole, through which composition can be pushed out, and on the opposite, second end there is lift, fitting internal surface of balloon and able to move to the first end. Non-therapeutic method of suppressing sweating or weakening body smell, including stage of topic application of composition on skin.
Antiperspirant and deodorant compositions / 2424789
Invention relates to field of cosmetics. Water-free antiperspirant or deodorant composition, which contains: particle of astringent antiperspirant salt; 20-90 wt % of oil-carrier, gelling agent for oil-carrier and moisturiser-polyol, moisturiser-polyol constituting 0.1-10% in terms of composition weight, polyethylene glycol has average molecular weight to 820. Product, containing composition is in distributing vessel, which contains balloon, on one end of which there is at least one hole, through which composition can be pushed out, and on the opposite, second end there is lift, fitting internal surface of balloon and able to move to the first end. Non-therapeutic method of suppressing sweating or weakening body smell, including stage of topic application of composition on skin.
Method of increasing antioxidant status of warm-blooded organism under ultraviolet irradiation / 2424580
20 minutes prior to an irradiation procedure in an ultraviolet chamber, an infusion tea of nettle, birch, plantain leaves is introduced orally in a laboratory animal. The infusion tea is prepared of leaves taken in the ratio 1:1:1, by keeping 8 g of the tea in boiling water 200 ml. The infusion tea is introduced at 5 ml/kg of weight daily for 28 days.
Composition and dosage form containing solid or semisolid matrix / 2423997
Composition for medical use contains a solid or semisolid matrix, at least one active ingredient uniformly dispersed therein. The matrix contains at least one pharmaceutically acceptable matrix-forming agent and compound 1,3-bis(lactamyl)butane, especially 1,3-bis(pyrrolidone-1-yl)butane. The active component has water-solubility less than 1 g/100 ml at 25°C. The active ingredient is preferentially dispersed in a matrix as a solid solution. The matrix-forming agent is chosen from a group of alcohol sugars, alcohol sugar derivatives, pharmaceutically acceptable polymers and their mixtures. The composition is used for preparing the pharmaceutical dosage forms for oral administration of the active ingredients.
Method of phytopreparation therapy of gastrointestinal diseases in calves / 2423996
Invention relates to veterinary science. The method involves a subcutaneous injection of reconvascelent blood serum containing rota- and coronavirus antihemagglutinins. It is combined with an intake of 70% alcoholate of a grinded herbal mixture containing equal proportions of purple Echinacea (Echinazea purpurea) herb and blossom clusters, Syrian rue (Peganum harmala) herb, tillet (Tilia cordata) blossom and common licorice (Glycyrrhiza glabra) roots. The alcoholate is prepared in the raw material to extractant relation 1:10, kept at temperature 15-20°C for 7 days. It is presented as 7-8% aqueous solution to be introduced in dosage 2.0-2.5 ml/kg of live weight every 12 hours to clinical recovery.
Method of phytopreparation therapy of gastrointestinal diseases in calves / 2423996
Invention relates to veterinary science. The method involves a subcutaneous injection of reconvascelent blood serum containing rota- and coronavirus antihemagglutinins. It is combined with an intake of 70% alcoholate of a grinded herbal mixture containing equal proportions of purple Echinacea (Echinazea purpurea) herb and blossom clusters, Syrian rue (Peganum harmala) herb, tillet (Tilia cordata) blossom and common licorice (Glycyrrhiza glabra) roots. The alcoholate is prepared in the raw material to extractant relation 1:10, kept at temperature 15-20°C for 7 days. It is presented as 7-8% aqueous solution to be introduced in dosage 2.0-2.5 ml/kg of live weight every 12 hours to clinical recovery.
Method of phytopreparation therapy of gastrointestinal diseases in calves / 2423996
Invention relates to veterinary science. The method involves a subcutaneous injection of reconvascelent blood serum containing rota- and coronavirus antihemagglutinins. It is combined with an intake of 70% alcoholate of a grinded herbal mixture containing equal proportions of purple Echinacea (Echinazea purpurea) herb and blossom clusters, Syrian rue (Peganum harmala) herb, tillet (Tilia cordata) blossom and common licorice (Glycyrrhiza glabra) roots. The alcoholate is prepared in the raw material to extractant relation 1:10, kept at temperature 15-20°C for 7 days. It is presented as 7-8% aqueous solution to be introduced in dosage 2.0-2.5 ml/kg of live weight every 12 hours to clinical recovery.
Amino acid preparation eliciting antitumor effect and method for its preparing / 2245143
Invention relates, in particular, to the development of an antitumor preparation based on natural substances. Invention relates to an amino acid preparation comprising at least one modified essential amino acid obtained by treatment of amino acid by ultraviolet radiation (UV) at wavelength 250-350 nm for 12-80 h at temperature 15-30oC or with ozone at temperature 15-25oC. The modified amino acid has no toxicity for health cells. Also, invention relates to a method for preparing such preparation. Invention provides the development of an antitumor preparation based on modified amino acids and expanded assortment of antitumor preparations being without cytotoxicity for normal cells.
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FIELD: chemistry. SUBSTANCE: invention relates to cosmetology and hair care compositions containing (i) emulsified particles of modified alkylsilicon, and (ii) emulsified particles of non-volatile silicon which does not contain alkyl modifying groups, wherein the modified alkylsilicon is liquid under normal conditions and has general formula (I): (CH3)3Si-O-[Si(CH3)(R)O]m-[Si(CH3)2O]n-Si(CH3)3 (I), where m assumes values from 1 to 450, n assumes values from 1 to 3000 and R is a monovalent alkyl radical containing 8-60 carbon atoms. EFFECT: composition provides efficient hair conditioning without undesirable strong deposition on hair. 6 cl, 2 ex, 2 tbl
The technical FIELD TO WHICH the INVENTION RELATES. The present invention relates to compositions for hair care products containing modified alkylsilane. BACKGROUND of INVENTION AND prior art Modified alkylsilane have found application in many cosmetic products, especially as humidifiers in products for skin care and as liabilitiesa additive in creams and lotions from the sun. In the patent WO91/09586 describes how certain polymethylphenylsiloxane can give your hair extra Shine and luster and gentleness and softness in the same way as polydimethylsiloxane, but which create a feeling that the hair outwardly less heavy and greasy. It is believed that these polymethylphenylsiloxane give hair more volume, fluffiness and softness thanks polydimethylsiloxane liquids. The authors of the present invention have observed that the modified alkylsilane of this type, as described in the patent WO91/09586, tend strongly deposited on the hair when used in a regular basis tools for hair care. Excessive deposition entails a reduction in the amount of hair that is perceived by many buyers is not desirable. The authors of the present invention have found that these problems can be is solved by combining emulsified particles modified alkylsilane with emulsified particles of a particular silicone, not containing alkyl modifying groups. The INVENTION The present invention provides a composition for hair care, containing: (i) emulsified particles of the modified alkylsilane, and (ii) emulsified particles of silicone, alkyl not containing modifier group. Compositions according to the invention provide an effective conditioning hair, considerably hair without overloading it. DETAILED DESCRIPTION Modified alkylsilane The composition of the present invention for hair care consists of emulsified particles of the modified alkylsilane. The term "modified alkylsilane" means crasneanscki polymer in which at least one alkyl group side chain having a length of hydrocarbon chain With6and above, deviates from at least one of the silicon atoms forming the main chain of the polymer. State of aggregation of the modified alkylsilanes under normal conditions mainly changes from wax to liquid depending on molecular parameters, such as long chain alkyl groups, including alkyl groups other than methyl) in the molecule and a molecular weight of the main chain of the silicone. The concept of "normal conditions"as used in this the overall work refers to the environmental conditions at a pressure of 1 atmosphere, 50% humidity and 25°C. Preferred modified alkylsilane for use in the present invention are liquid under normal conditions. Preferred modified alkylsilane for use in the present invention have an average molecular weight (Mn)whose value varies from 10,000 to 450,000, most preferably up to 110000 60000 daltons. Suitable modified alkylsilane for use in compositions for hair care products of the present invention can be chemically characterized by the General formula (I)
where m takes values from 1 to 450, n takes values from 1 to 3000, and R is a monovalent alkyl radical comprising from 8 to 60 carbon atoms. In the General formula (I), -[Si(CH3)2O] - part of the molecule is usually chaotic intertwined with the -[Si(CH3)(R)O] - parts of the molecule, m and n are, as a rule, are average values because of the nature of the polymerization process. Preferred substances of the General formula (I) for use in the present the invention have the value of m, ranging from 40 to 100, more preferably from 50 to 80. Preferred substances of the General formula (I) for use in the present invention have a value of n ranging from 500 to 1400, more preferably from 700 to 1200. Preferred substances of the General formula (I) for use in the present invention have a ratio of m:n, varying from 15:85 to 1:99, more preferably from 10:90 to 5:95. In the preferred substances of the General formula (I) for use in the present invention R is a linear alkyl radical having from 8 to 22, more preferably from 8 to 14, and most preferably from 10 to 12 carbon atoms. Methods for production of modified alkylsilanes suitable for use in this invention are well known in the art and described, for example, in patents EP 495596 and WO91/09586. Modified alkylsilane suitable for use in this invention are also commercially available from such suppliers of silicones as the Corporation Momentive Performance Materials (Wilton, Connecticut, USA) and Dow Corning (Midland, Michigan, USA). Modified alkylsilane present as emulsified particles in the composition for hair of the present invention. Emulsified particles modified alkylsilane in the composition of this invention can generally be crenidium particles on Sauter (D 3,2), ranging from 0.1 to 10, preferably from 1 to 4 micrometers. A suitable method for measuring the average diameter of the drops on Sauter (D3,2) is the scattering of laser radiation using such a device, as a Malvern Mastersizer. Mixtures of any of the above modified alkylsilanes may also be used. Modified alkylsilane for use in this invention are available as pre-obtained emulsions of silicone from suppliers of silicones, such as those mentioned above. The use of such pre-obtained emulsions of silicone is preferable because of the simplicity of the manufacture and control over the particle size of the silicone. Such pre-obtained emulsion of silicone will typically further include a suitable emulsifier, such as anionic or nonionic surfactant, and can be prepared by chemical emulsification, for example by emulsion polymerization, or by mechanical emulsification using a stirrer with large shear forces. The total number of modified alkylsilane in compositions for hair care products of the present invention, in General, varies from 0.01 to 5%, preferably from 0.05 to 2%, more preferably from 0.1 to 1.5% modified alkylsilane the and of the total mass of the composition. Non-volatile silicones, alkyl not containing modifier group In the composition for hair of the present invention are emulsified particles of non-volatile silicone, alkyl not containing modifier group. The term "nonvolatile"as used here, means that the substance in question has a vapor pressure under normal conditions of 0.2 mm Hg or less, preferably about 0.1 mm Hg or less. Under "silicone, alkyl not containing modifier group, in General, imply polyorganosiloxane, which does not contain any lateral alkyl groups having long hydrocarbon chain With6or more, or when one of the silicon atoms forming the main polymer chain. Suitable non-volatile silicones, alkyl not containing the modifying groups, which can be used in the present invention have a viscosity ranging from 350 to 200000000 mm2s-1at 25°C. Preferably, the viscosity was at least 5000, more preferably at least 10000 mm2s-1at 25°C. Preferably, the viscosity does not exceed 20000000, more preferably 10000000, most preferably 5000000 mm2s-1at 25°C. All viscosity values mentioned herein are kinematics the mi viscosities, except in those cases where it is stipulated, and are usually provided by suppliers of silicones or as measured at 25°C using a calibrated glass capillary viscometer in terms of itself, or as calculated from the molecular weight of the substances. Suitable non-volatile silicones, alkyl not containing the modifying groups, for use in the present invention have an average molecular weight (Mn)ranging from 10000 to 1000000, more preferably from 100,000 to 500,000 daltons. Suitable non-volatile silicones, alkyl not containing the modifying groups, for use in compositions for hair care products of this invention can be chemically characterized by the General formula (II)
where each R may be C1-4the alkyl or aryl, x means the number from 200 to 8000, and maybe With1-4the alkyl, C1-4alkoxyl, aryl, alloxylon or hydroxyl. In the preferred substances of the General formula (II) for use in this invention all R groups are methyl, And both groups are either methyl or hydroxyl. Such substances are named "dem is ticon" and "dimethiconol", respectively, according to the Association for perfume and cosmetic products and fragrances (CTFA). More preferably, all R groups be methyl, And both groups are hydroxyl. Also suitable as the nonvolatile silicones, alkyl not containing the modifying groups, for use in compositions for hair care products of this invention are polydimethylsiloxane with functional amino group, and which have the name "amodimethicone" according to the Association for perfume and cosmetics (CTFA) goods and fragrances, and the General formula (III)
in which R means that CH3or OH, x and y are independent integers from 1 and up, R1and R2each can be alkalinous group having from 2 to 5 carbon atoms. Also suitable as the nonvolatile silicones, alkyl not containing the modifying groups, for use in compositions for hair care products of this invention are polydimethylsiloxane with functional amino group with the name "trimethylsilylamodimethicone" according to the Association for perfume and cosmetic products and fragrances (CTFA), and General formula (IV) tr>
where x and y are mean independent of the number 1 and the other, R1and R2each independently is alkalinous group having from 2 to 5 carbon atoms. Mixtures of any of the above non-volatile silicones, alkyl not containing the modifying groups may also be used. Non-volatile silicone, alkyl not containing the modifying groups, present in the form of emulsified particles in the composition for hair of the present invention. Emulsified particles of non-volatile silicone, alkyl not containing the modifying groups may generally be in the composition of the present invention, the average particle diameter on Sauter (D3,2), which varies from 0.01 to 10, preferably from 0.1 to 5, more preferably from 0.5 to 2.5 micrometers. Non-volatile silicones, alkyl not containing the modifying group, for use in the compositions of this invention are available as pre-obtained emulsions of silicone from suppliers of silicones, such as those mentioned above. The use of such pre-obtained emulsions of silicone is preferable because of the simplicity of technologiesdocument and controlling the particle size of the silicone. Such pre-obtained emulsion of silicone will typically further include a suitable emulsifier, such as anionic or nonionic surfactant, and can be prepared by chemical emulsification, for example by emulsion polymerization, or by mechanical emulsification using a stirrer with large shear forces. Examples of pre-obtained emulsions of silicone are 1784 emulsion Dow Corning®and 1785 emulsion Dow Corning®. Both of these emulsion is an anionic emulsion of dimethiconol. The total number of non-volatile silicone, alkyl not containing the modifying groups, in compositions for hair care products of the present invention, in General, varies from 0.1 to 10%, preferably from 0.5 to 5%, more preferably from 1 to 3% of non-volatile silicone, alkyl not containing the modifying groups to the total weight of the composition. In the composition of the present invention the weight ratio of the modified alkylsilane (as defined above) to a non-volatile silicone, alkyl not containing the modifying groups (as defined above), in General, varies from 10:1 to 1:10, preferably from 1:1 to 1:10, more preferably from 1:2 to 1:8. Product form Compositions of the present invention are typically "see the line" songs, which are applied to the hair, and then washed. The most preferred form of the compositions according to the present invention is a conditioner for hair care (usually after shampooing) and then rinse. The composition of the conditioning Air conditioning according to this invention will typically contain one or more cationic surfactants, which are valid in cosmetology and is suitable for topical application to the hair. Suitable cationic surfactants have the formula [N(R1)(R2)(R3)(R4)]+(X)-in which R1, R2, R3and R4are independently from each other (C1-C30) alkyl or benzyl radical, X is a salt-forming anion, which is a halogen, acetate, citrate, lactate, glycolate, phosphate, nitrate, sulfate and methosulfate. Preferably, one, two, or three R1, R2, R3and R4are independently from each other (C4-C30) alkyl radical and the other R1, R2, R3and R4the group or groups are (C1-C6) alkyl or benzyl radicals. More preferably, one or two R1, R2, R3and R4are independently from each other (sub> 6-C30) alkyl radical and the other R1, R2, R3and R4the groups were (C1-C6) alkyl or benzyl radicals. Additionally, the alkyl group may consist of one or more ester (-OCO - or-COO-) and/or ether (-O-) linkages in the alkyl chain. Alkyl groups can optionally be substituted by one or more hydroxyl groups. Alkyl groups can be straight or branched chain and alkyl groups having 3 or more carbon atoms, cyclic chain. Alkyl groups can be saturated or contain one or more carbon-carbon double bonds (for example, oleilove group). The alkyl group may be arbitrarily amoxillian in the alkyl chain one or more ethylenoxide. Examples of suitable cationic surfactants for use in compositions of the air conditioner according to the present invention are cetyltrimethylammonium chloride, beginelementary chloride, pyridinium chloride, Tetramethylammonium chloride, tetraethylammonium chloride, octyltrimethoxysilane chloride, dodecyltrimethylammonium chloride, hexadecyltrimethylammonium chloride, octylbenzene chloride, delldimension chloride, stearylamine salamone chloride, didodecyldimethylammonium chloride, dictatorially chloride, colortripletorname chloride, digidrirovanny taly of dimethylammonium chloride (for example, Arquad 2HT/75 from Akzo Nobel), cocontributions chloride, PEG-2-alimony chloride and the corresponding hydroxides of the above-mentioned compounds. Other suitable cationic surfactants are substances having denote Quaterni-5, Quaternium-31 and Quaternium-18, adopted by the Association of perfumery and cosmetic products and fragrances (CTFA). Particularly useful cationic surface-active agent for use in air conditioners according to the invention is cetyltrimethylammonium chloride, commercially available, for example, GENAMIN CTAC from Hoechst Celanese. Other particularly useful cationic surface-active agent for use in air conditioners, according to this invention, is beginelementary chloride, commercially available, for example GENAMIN KDMP from the company Clariant. Another example of a class of suitable cationic surfactants used in the present invention, is the combination of (i) and (ii)given below: (i) amidoamine corresponding to General formula (I)
in which R1represents an acyclic hydrocarbon chain of varying degrees of saturation, having 10 or more carbon atoms, R2and R3independently from each other selected from acyclic hydrocarbon chains of varying degrees of saturation, having from 1 to 10 carbon atoms, and m means it is a number from 1 to 10, and (ii) acid. Used herein, the term " acyclic hydrocarbon chain of varying degrees of saturation means alkyl or alkenylphenol chain. Preferred aminoamide compounds are compounds corresponding to the formula (I), in which R1is an acyclic hydrocarbon residue of varying degrees of saturation, having 11 to 24 carbon atoms, R2and R3each is independently from each other selected acyclic hydrocarbon residues of varying degrees of saturation, preferably alkyl groups having from 1 to 4 carbon atoms, and m denotes a number from 1 to 4. Preferably, R2and R3are methyl or ethyl groups. Preferably, m is 2 or 3, i.e. ethylene or propylene group. Amidoamine, which are preferred, include stearamidopropyl, stearamidopropyl, stearoylethanolamine is in, stearoylethanolamine, polymethylenepolyphenylene, polymethylenepolyphenylene, polymethylmethacrylate, polymethylmethacrylate, regenerateExpiredSessionId, beynelmilelcilerinin, beynelmilelcilerinin, beynelmilelcilerinin, archivereorganisation, archivearticle, archivearticle, arginineminocycline, and mixtures thereof. Amidoamine, which are preferred, are stearamidopropyl, stearoylethanolamine and mixtures thereof. Commercially available amidoamine are stearamidopropyl under the trademarks LEXAMINE S-13, which can be enjoyed in the company Inolex (Philadelphia, Pensylvania, USA) and AMIDOAMINE MSP, which can be enjoyed in the company Nikko (Tokyo, Japan), stearoylethanolamine under the trademark AMIDOAMINE S, which can be enjoyed in the company Nikko, regenerateExpiredSessionId under the trademark INCROMINE BB, which can be enjoyed in the company Croda (North, Numberside England), and various amidoamine under the trademark SCHERCODINE, which can be enjoyed in the company Scher (Clifton, New Jersey, USA). Acid (ii) can be any organic or inorganic acid capable to proteinopathy amidoamine in composition tools for hair care. Suitable acids are hydrochloric acid, UKS is SNA acid, tartaric acid, fumaric acid, lactic acid, malic acid, succinic acid and mixtures thereof. Preferably the acid is selected from the group consisting of acetic acid, tartaric acid, hydrochloric acid, fumaric acid, and mixtures thereof. The primary role of the acid is protonation of amidoamine in the composition means for care of hair, forming a tertiary amine salt (TAS) directly in the composition tools for hair care. TAS, in essence, is unstable cationic surface-active agent containing a Quaternary ammonium or pseudoterminal ammonium. Accordingly, the acid is present in sufficient quantity to proteinopathy all amidoamine available, namely in the amount of at least equimolar number amidoamine present in the composition. Mixtures of any of the above cationic surfactants can also be used. In air conditioners of the present invention, the level of cationic surfactant is, in General, vary from 0.01 to 10%, more preferably from 0.05 to 7.5%, most preferably from 0.1 to 5% cationic surfactants by weight of the total composition. Air conditioners of the present invention usually contain fatty alcohol. I believe that the transmission is Noah the use of fatty alcohols and cationic surfactants in the compositions of air conditioners is particularly beneficial because leads to the formation of kamilaroi phase, in which the cationic surfactant dispergirovannom. Typical fatty alcohols containing from 8 to 22 carbon atoms, more preferably from 16 to 22. Fatty alcohols are mainly compounds containing unbranched alkyl groups. Examples of suitable fatty alcohols are cetyl alcohol, stearyl alcohol and mixtures thereof. The use of these substances has the advantage in that they contribute to the conditioning properties of the compositions of this invention. The level of fatty alcohol in air conditioners of this invention will generally range from 0.01 to 10%, preferably from 0.1 to 8%, more preferably from 0.2 to 7%, most preferably from 0.3 to 6% by weight of the total composition. The mass ratio of cationic surfactant to fatty alcohol ranges, respectively, from 1:1 to 1:10, preferably from 1:1.5 to 1:8, optimally from 1:2 to 1:5. If the mass ratio of cationic surfactant to fatty alcohol is too high, it can lead to eye irritation from this composition. If it is too low, it makes your hair, according to some buyers, scratchy to the touch. Another preferred form of the product is the song for shampoos. The composition of the shampoo The composition of the shampoos of the present invention, generally, are aquatic, meaning they contain water or an aqueous solution, or a lyotropic liquid crystal phase as a main component. Accordingly, the composition will contain from 50 to 98%, preferably from 60 to 90% water by weight of the total composition. Anionic cleansing surfactant The composition of the shampoos according to the invention will generally contain one or more anionic cleansing surfactants which are commercially available and suitable for topical application to the hair. Examples of suitable anionic cleansing surfactants are the alkyl sulphates, alkylarylsulfonate, alkylarylsulfonate, alcoholization, alkylacrylate, alkylsulfonate, alkylarylsulfonate, N-allylcarbamate, alkylphosphate, alkylphosphate, and alkyl ether carboxylic acids and their salts, especially their sodium, magnesium, ammonium and mono-, di - and triethanolamine salt. The alkyl and acyl groups contain mainly from 8 to 18, preferably from 10 to 16 carbon atoms and may be unsaturated. Alkylarylsulfonate, alkylarylsulfonate, alkylphosphate and alkyl ether carboxylic acids and their salts may contain from 1 to 20, edit the CI of ethylene oxide or propylene oxide in the molecule. Common examples of anionic cleansing surfactants for use in the shampoo compositions of the present invention are oleylamine sodium, laurylsulphate ammonium, sodium lauryl sulfate, esterified sodium lauryl sulfate, the esterified laurylsulphate sodium lauryl ammonium, esterified lauryl ammonium, dodecylbenzenesulfonate sodium, cocoylisethionate sodium, laurelsatin sodium, esterified laurikkala acid and N-laurylsarcosine sodium. Suitable anionic cleansing surfactants are sodium lauryl sulphate, esterified sodium lauryl sulphate (n)EO, (where n is from 1 to 3), the esterified laurylsulphate sodium (n)EO, (where n is from 1 to 3), lauryl ammonium, esterified lauryl ammonium (n)EO, (where n is from 1 to 3), cocoylisethionate sodium and etherification laurikkala acid (n)EO, (where n is from 10 to 20). Can also be used mixtures of any of the above-mentioned anionic cleansing surfactants. The total number of anionic cleansing surfactant in the compositions of the shampoos of the present invention, in General, varies from 0.5 to 48%, preferably from 1.5 to 35%, more preferably from 5 to 20% of Union the th cleansing surfactant by weight of the total composition. Additional ingredients Optionally, the shampoo composition of the invention may contain additional ingredients as described below, to enhance the effect and/or consumer acceptance. Co-surfactant The composition may contain co-surfactants aesthetic, physical or cleansing properties to the composition. An example of a co-surfactant is a nonionic surfactant that may be contained in amounts ranging from 0.5 to 8%, preferably from 2 to 5% of the total weight of the composition. For example, a typical non-ionic surfactants that can be included in compositions of the shampoos of this invention are condensed products (C8-C18) aliphatic primary or secondary linear or branched chain alcohols or phenols with accidentally, usually ethylene oxide and generally having from 6 to 30 ethyleneoxide groups. Other typical non-ionic surfactants are mono - and dialkylacrylamide. Examples are cocolonization and colordialed and cocolonization. Additional nonionic surfactants that can be used in the compositions is the second shampoos of the present invention, are alkylpolyglucosides (APGs). Usually APG is this substance which consists of an alkyl group linked (optionally via a bridging group) with a group of one or more helicoiling groups. Preferred APGs are defined by the following formula: RO-(G)n, where R is an alkyl group branched or straight chain which may be saturated or unsaturated, and G is sacharides group. R may be the average alkyl chain length from about5to about20. Preferably, R was the average alkyl chain length from about8to about12. Most preferably, the R value was between about 9.5 and about 10.5. G can be selected from C5or6monosaccharide residues, and it is preferable that was glycoside. G can be selected from the group consisting of glucose, xylose, lactose, fructose, mannose and derivatives thereof. It is preferable that G was glucose. The degree of polymerization, n can take values from about 1 to about 10 and more. Preferably, the value of n is from about 1.1 to about 2. Most preferably, the value of n is from about 1.3 to about 1.5. Suitable alkylpolyglycoside for use in the present invention are commercially available and include, for example, such substances are referred to as: Oramix NS10 from the company Seppic, Plantaren 1200 and Plantaren 2000 from Henkel. Other non-ionic surfactants derived sugar that can be used in the compositions of the present invention contain (C1-C6N-alkyl With10-C18polyhydroxyamide fatty acids, such as C12-C18N-methylglucamide, as described in the example in the patent application WO 92 06154 patent US 5194639, and N-alkoxyalkane fatty acids, such as C10-C18N-(3-methoxypropyl)glycemic. A preferred example of the co-surfactant is amphoteric or zwitterionic surfactant, which may enter into the composition in an amount ranging from 0.5 to about 8%, preferably from 1 to 4% of the total weight of the composition. Examples of amphoteric or zwitter-ionic surfactants are alkylamines, alkylbetaine, alkylamidopropylbetaine, alkylsulfonates (Sultanate), allylglycine, alkylcarboxylic, alkylamidoamines, alkylamidoamines, alcelaphinae, alkylamidopropylbetaine, allcounty and acellularity, where the alkyl and acyl groups have from 8 to 19 carbon atoms. Typical amphoteric and zwitterionic surfactants used in shampoos of the present invention include laurylamine, cocodimama sulfopropyl, laurylether, cocamidopropylbetaine and cocoamphoacetate sodium. The most preferred amphoteric or zwitter-ionic surface-active agent is cocamidopropylbetaine. Mixtures of any of the above amphoteric or zwitter-ionic surfactants may also be used. Preferred mixtures are mixtures of cocamidopropylbetaine with additional amphoteric or zwitter-ionic surfactants, which are described above. Preferred additional amphoteric or zwitter-ionic surface-active agent is cocoamphoacetate sodium. The total amount of surfactant (including any co-surfactant, and/or any emulsifying ingredient in shampoo compositions of the present invention, in General, is from 1 to 50%, preferably from 2 to 40%, more preferably from 10 to 25% surfactant by weight of the composition. Cationic polymers Cationic polymers are desirable components of the shampoo composition of the present invention to improve air conditioning systems. Suitable cationic polymers may be homopolymers, which are kationozameshchennykh or can be obtained from two or more kinds of monomers. The average molecular the th weight (M w) polymers, in General, is in the range between 100,000 and 2 million daltons. The polymers will have cationic nitrogen-containing groups, such as Quaternary ammonium or protonated amino groups, or mixtures thereof. If the molecular weight of the polymer is too low, then the effect of conditioning is bad. If it is too high, then there may be problems of high bulk viscosity, leading to thickening of the composition when it is poured. Cationic nitrogen-containing group will mainly be present as a substituent in the fraction of the total Monomeric parts cationic polymer. Therefore, when the polymer is not homopolymer, it may contain intermediate nicotianae monomer units. Such polymers are described in the Handbook of cosmetic ingredients (the Cosmetic Ingredient Directory), 3rd edition, Association of perfumery and cosmetic products and fragrances (CTFA). The ratio of cationic to negationem the Monomeric units selected in order to give polymers having a cationic charge density in the desired range, which is usually from 0.2 to 3.0 mEq/g, the Density of cationic charge of the polymer is properly determined according to the method of kildala, as described in the US Pharmacopoeia (Pharmacopies USA), in the section of chemical tests for the determination of nitrogen. Suitable cationic polymers which are, for example, copolymers of vinyl monomers having cationic amino - or Quaternary ammonium functional groups with water soluble spacer elements monomers such as (meth)acrylamide, alkyl - and dialkyl(meth)acrylamide, alkyl(meth)acrylate, vinylcaprolactam and vinylpyrrolidone. Alkyl and dialkylamino monomers, preferable are C1-C7 alkyl groups, more preferably C1-3 alkyl group. Other suitable spacers are complex, vinyl esters, vinyl alcohol, maleic anhydride, propylene glycol and ethylene glycol. Cationic amines can be primary, secondary or tertiary amines, depending on individual types and the pH of the composition. In General, secondary, and tertiary amines, in particular tertiary, are preferred. Amines, substituted vinyl monomers and amines, can be polymerized in the amine form, and then converted into ammonium by quaternization. Cationic polymers can contain a mixture of monomer units derived from substituted monomer amine and/or Quaternary ammonium, and/or a compatible spacer elements monomers. Suitable cationic polymers include, for example: - polymers containing cationic vallely Quaternary ammonium, including, for example, chloride homopolymer dimethyldiallylammonium, and copolymers of acrylic is and chloride of dimethyldiallylammonium, having in the industry (CTFA) the following names Polyquaternium 6 and Polyquaternium 7, respectively; - inorganic acid salt aminoalkyl esters of Homo - and copolymers of unsaturated carboxylic acids having 3 to 5 carbon atoms (as described in US patent 4009256); cationic polyacrylamides (as described in the patent WO95/22311). Other cationic polymers that may be used are cationic polymers, polysaccharides such as cationic cellulose derivatives, cationic starch derivatives, and cationic derivatives of the guar resin. Cationic polysaccharide polymers, which are suitable for use in the compositions of this invention include monomers of the following formula: A-O-[R-N+(R1)(R2)(R3X-], where a represents a group anhydroglucose residue, such as starch or cellulose anhydroglucose residue, R is alkilinity, oxyalkylene, polyoxyalkylene, or hydroxyalkyloxy group, or their combination. R1, R2and R3independently represent alkyl, aryl, alcylaryl, arylalkyl, alkoxyalkyl or alkoxyaryl groups, each group contains up to about 18 carbon atoms. Preferably, the total number of carbon atoms for each cationic fragment (i.e., the amount of carbon is different atoms in R 1, R2and R3) is about 20 or less, and X is an anionic counterion. Another type of cationic cellulose includes the polymeric Quaternary ammonium salt of hydroxyethyl cellulose, entered into interaction with lauryldimethylamine the epoxide, referred to in the technique (CTFA) Polyquaternium 24. These materials are available from Amerchol Corporation, for example, under the trademark Polymer LM-200. Other suitable cationic polysaccharide polymers include Quaternary nitrogen-containing cellulose ethers (for example, as described in US patent 3962418) and copolymers of etherified cellulose and starch (for example as described in US patent 3958581). A particularly suitable type of cationic polysaccharide polymer, which can be used is a cationic derivative of the guar resin, such as qualitatsprodudukten chloride (commercially available in the company Rhodia in their series of products under the trademark JAGUAR). Examples of such substances are JAGUAR C13S, JAGUAR C14, JAGUAR C15, JAGUAR C17, JAGUAR C16, JAGUAR SNT and JAGUAR S. Mixtures of any of the above cationic polymers can be used. The cationic polymer is, in General, be present in the shampoo compositions of the present invention in amounts of from 0.01 to 5%, preferably from 0.05 to 1%, more preferably from 0.08 to 0.5% of the cationic polymer to the total weight of the comp the flies. Suspendisse agent Preferably, the composition is an aqueous shampoo of the present invention further comprises suspendisse component. Suitable suspendresume components selected from polyacrylic acids, cross-linked polymers of acrylic acid, copolymers of acrylic acid with a hydrophobic monomer, copolymers of carboxylic acid monomers and esters of acrylic acid, cross-linked copolymers of acrylic acid and esters of acrylic acid, heteropolysaccharide resins and crystalline long chain acyl derivatives. Long chain acyl derivative, if necessary, is selected from glycol stearate, alkanolamide fatty acids having from 16 to 22 carbon atoms and mixtures thereof. Distearate of ethylene glycol and polyethylene glycol-3-distearate are the preferred long-chain acyl derivatives, as they give a pearlescent effect of the composition. Polyacrylic acid commercially available as Carborol 420, Carborol 488 or Carborol 493. Polymers of acrylic acid cross-linked with a polyfunctional agent, can also be used; they are commercially available as Carborol 910, Carborol 934, Carborol 941 and Carborol 980. An example of a suitable copolymer of carboxylic acid containing monomer and the acrylic acid-ester is Carborol 1342. All connections Carborol (t is RGBA brand) commercially available from the company Goodrich. Suitable cross-linked polymers of acrylic acid and esters of acrylic acid are Pemulen TR1 and Pemulen TR2. Suitable heteropolysaccharides resin is xanthan gum, for example, which is commercially available as Kelzan mu. Mixtures of any of the above suspendida agents can be used. Preferred is a mixture of cross-linked polymer of acrylic acid and crystalline long-chain acyl derivative. Suspendisse agent will, in General, be present in the shampoo compositions of the invention in amounts of from 0.1 to 10%, preferably from 0.5 to 6%, more preferably from 0.9 to 4% of a suspending agent by weight of the total composition. Additional conditioning agents Compositions of the invention can contain additional conditioning agents in addition to the substances described above, in order to optimize the advantages of wet and dry conditioning. Examples of additional conditioning agents are volatile silicones. The term "volatile"as used here, means that the substance has a vapor pressure under normal conditions is equal to or higher than that of ethanol. Volatile silicones suitable for use in compositions of the present invention include both linear and cilice is such silicones. Linear volatile silicones will generally have viscosity 5 mm2s-1(CST) or less at 25°C., while the cyclic volatile silicones are, as a rule, have a viscosity of 10 mm2s-1or less at 25°C. Suitable cyclic volatile silicones include Cyclopentasiloxane, such as cycloalkylcarbonyl and cycloalkylcarbonyl, where alkyl and CNS groups contain From1-C8alkyl groups. The General formula of suitable cyclic volatile silicones is the following: [(R1)(R2Si-O-]n, in which n is from 3 to 7, and R1and R2independently selected from alkyl With1-C8, aryl (in particular phenyl) and alkaryl (for example, C1-C8substituted aryl). Preferably, R1and R2are1-C2alkilani. Most preferably, R1and R2are1the alkyl (such substances are CFTA designation cyclomethicone). Preferably, n is equal to the value of 4 to 6, most preferably 4 to 5. Specific examples of preferred cyclic volatile silicones are octamethylcyclotetrasiloxane, dimethylcyclopentane and their mixture. Linear volatile silicones include polyorganosiloxanes, such as polydiorganosiloxane and polyalkylacrylate. The General formula for the appropriate linear volatile silicones are the following: (R1)(R2)(R3Si-O-[Si(R4)(R5)O]nSi(R6)(R7)(R8), in which n is equal to values from 1 to 7, and R1, R2, R3, R4, R5, R6, R7and R8are1-C2alkilani. More preferably, R1, R2, R3, R4, R5, R6, R7and R8was1the alkyl (such substances are CFTA designation Dimethicone). Silicones of the above described types of commercially available, for example, from Dow Corning Corporation as DC 244, 245, 344, 345 and 200. Other optional ingredients The composition of the present invention may contain other ingredients to improve and/or consumer acceptance. Such components include fragrances, dyes and pigments, substances that regulate the pH of the medium, the substance that gives the pearl effect and cloud emulsions, viscosity modifiers, preservatives and natural nutrients for hair, such as botanicals, fruit extracts, sugar derivatives and amino acids. Method of use The compositions of this invention are primarily intended for topical application to the hair and/or scalp of a person in compositions for washing, in order to better t the VA hairline, such as moisturizing hair, smoothness, softness, flexibility, manageability and Shine. Compositions presented in the present invention, generally are conditioning compositions for hair care (usually after shampooing) with subsequent flushing. Or compositions presented in the invention can be aqueous compositions shampoos used by massaging them into the hair, followed by flushing with clean water before drying the hair. Optionally, a separate conditioning composition can be used after washing to drying, but this may not be necessary, as it is assumed that the composition of water shampoo invention provides both cleansing and conditioning the hair. This invention is further illustrated by reference to the following, non-limiting examples in which all percentages are mass of the total weight, except in those cases where specified. Examples of the invention are numbered. Comparative examples not in accordance with this invention) are indicated by letters. EXAMPLES Composition for conditioning hair was prepared having ingredients as shown in the following table 1:
The compositions of table 1 were evaluated for their ability to straighten the hair and on the deposition of silicone on the hair. To study hair straightening test composition is applied to hair lining with the hair standard weight and volume. Make pictures as soon as these pads are dried under controlled conditions. Experts are asked to make pairwise comparisons of the degree of discrepancy n the clutches of these photos with the sample. Done 36 comparisons for each test composition. The deposition of silicone was measured by x-ray fluorescence spectroscopy. Also measured the amount of hairpieces after processing the test compositions. The results of the above analyses are presented in the following table 2:
For mismatch scoring for the hair of the smallest ball score is preferred. It is also desirable to avoid excessive levels of silicone deposition on hair. From the above data you can see how high levels of silicone deposition correlate with reduced dimensions of the overlay. Example 1 (according to the invention) and Examples A-C (comparative) all used a modified alkylsilane(3)at various activity levels. Within these series Example 1 and Example To give the best (i.e. lowest) discrepancy score for the hair. However, the Example demonstrates junk 11-fold increase in the deposition of silicone on the hair and significantly reduces the volume of the pads, as compared with Example 1. Example 2 (according to the invention) and examples D-F (comparative) all use a modified alkylsilane(4)at various activity levels. Within these series Example 2 and Example F give the best (i.e. lowest) discrepancy score for the hair. However, the Example F shows unwanted 24-KRA is increase of deposition of silicone and significantly reduces the volume of the pads, compared with Example 2. Comparative Example G gives this level of deposition of silicone, which is approximately equal to the level of Example 2. However, the characteristics of the Example G mismatch ball estimates for the hair significantly inferior to those same characteristics of Example 2. Therefore, the compositions of this invention provide excellent balance alignment hair, deposition of silicone and the amount of hair in comparison with comparative examples. 1. Composition for hair care, containing: 2. The composition according to claim 1, in which R is a linear alkyl radical containing from 10 to 12 carbon atoms. 3. The composition according to any one of claims 1 or 2, in which the non-volatile silicone, alkyl not containing the modifying groups has the General formula (II) 4. The composition according to claim 3, in which all R groups are methyl, And both groups are hydroxyl. 5. The composition according to claim 1, in which the mass ratio of the modified alkylsilane to non-volatile silicone, alkyl not containing the modifying groups, varies from 1:2 to 1:8. 6. The composition according to claim 1, which is conditioned to handle hair (after shampooing) and then rinse.
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