MXPA97005154A - Composition for personal cleaning antibacterial liquid three in one with generation of ultra foam - Google Patents
Composition for personal cleaning antibacterial liquid three in one with generation of ultra foamInfo
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Abstract
The present invention relates to a mild antibacterial composition for personal cleansing in liquid form, (more specifically, compositions with foam generation, soft, especially those that are useful in the application to the body, face and hands) comprising :( a) from about 0.1 parts to about 20 parts, preferably from 1 part to 15 parts, especially from 3 parts to 12 parts by weight of anionic surfactant, (from about 0.1 part to about 20 parts, preferably from 1 part to 15 parts, especially from 3 parts to 12 parts by weight of amphoteric surfactant, (c) from about 0.5 parts to about 25 parts, preferably from 0.5 parts to 15 parts, especially from 3 parts to about 10 parts by weight of a skin moisturizer in form of oil, preferably an adduct prepared from vegetable oils containing this s unconjugated polyunsaturated fatty acids which are conjugated and elaidinized and then modified by the addition of Dieis-Alder, with a member of the group consisting of acrylic acid, fumaric acid and maleic anhydride, (d) from about 0.1 parts to about 2.0 parts of antibacterial agent, and (e) water, wherein the anionic surfactant and the amphoteric surfactant together comprise from about 0.5 part to about 30 parts, preferably from 5 parts to 25 parts, especially from 10 parts to 20 parts. by weight of the composition, and where the weight ratio of the amphoteric surfactant anionic surfactant, is within the range of from about 1: 5 to about 20: 1, preferably from 1: 2 to about 5: 1, especially from 1: 1 to about 2
Description
COMPOSITION FOR ANTIBACTERIAL LIQUID PERSONAL CLEANING THREE IN ONE WITH GENERATION OF
ULTRA SOFT FOAM
BACKGROUND OF THE INVENTION Field of the Invention The present invention relates to mild antibacterial compositions for personal cleansing in liquid form. More specifically, the present invention relates to soft, foaming compositions, especially those that are useful for application to the body, face and hands. BACKGROUND OF THE INVENTION The cleaning of the skin, carried out with active surface cleaning preparations, has become a point of great interest. Many people wash and rub their skin with different active surface preparations several times a day. Cleaners in liquid form are highly preferred, especially for use in the body, due to the convenience and to not dirty the toilets and bathrooms in general. The antibacterial cleansers for personal cleansing are preferred because they kill germs. Gentle cleansers for personal cleansing are those that are desired to minimize skin irritation, dryness, etc. It would be very desirable, a personal cleansing product, having these three preferred characteristics. Cleansers for the skin, should clean the skin gently, cause little or no irritation, without drying the skin after frequent use. Certain synthetic surfactants are particularly mild. However, the main drawback of soft synthetic surfactant systems in liquid form is that when they are formulated to cleanse the skin, they have poor foam generation. Compared with soap bars of the highest standards (bars that are rich in coconut soap and high in fat), these surfactant formulations in liquid form of the prior art, either have a poor foam generation, or provide very little softness to the skin. As expected, the generation of foam is a function of the selection of the surfactant and its concentration. The conceivable amount of surfactant compositions in liquid form formulated with or without skin sensing agents is numerous. The rheological and phase properties are exhibited by very extensive prototypes (for example, thin liquids, gels, coarse pastes, solutions, emulsions). The phase stability of the prototypes is very acceptable in short periods of time, but over a prolonged period of time, only a small fraction of them retain their original properties and acceptability. See, for example, US Patents Nos .: 4,338.21 1, issued to Stíros, issued on July 6, 1982; 4,310,433, granted to Stiros, issued on January 12, 1982; and 4,842,850, granted to Vu, issued June 27, 1989, which have been incorporated into the present description as a reference. As a simple variable, the optimization of foam generation is a completely simple process. The use of highly foamed anionic surfactants that are known, with foam propellants produce an acceptable volume of foam. Unfortunately, the most foaming anionic surfactants are also generally those that produce the most irritation in the skin, and are the worst in terms of clinical smoothness. Surfactants that are among the most mild with minimal skin irritation, such as sulfate (NH4AE12S) of ammonium lauryl ether (12 EO), are extremely deficient in foam generation. These two facts separately, make the selection of the surfactant and optimization process in foam propulsion, is an act of delicate balance. See, for example, U.S. Patent No. 4,338.21 1, supra, which is incorporated herein by reference. The introduction of an antibacterial in the balance of the composition, results in additional softness problems, foam generation, and efficiency. As reported in the commercial literature, certain ethoxylated non-ionic mild surfactants, for example, Tween® 80 (ICI Americas, Inc.), and lecithin have deactivating effects in the desgermenisation of a preferred antibacterial, Triclosan (Irgansan® DP 300, which we also refer to in this document as "TCS"), according to the Irgasan Trade Bulletin DP 300 of 1988 of Ciba-Geigy. In fact, there are some strict requirements for skin cleansers, which limit the choice of active surface and antibacterial agents, and as a result, the final desgermenisation formulations represent a degree of compromise. The softness is often obtained at the expense of effective desgermenisation or effective cleaning, and the generation of foam can be sacrificed, either by the softness, the stability of the product, or both.
The present invention offers a valuable combination of desirable properties for skin cleansing formulations in liquid form. Accordingly, it is an object of the present invention to develop skin cleansing compositions in liquid form, which exhibit improved softness, good cleansing and foaming, and good desgering properties. Other objects of the present invention will be appreciated from the following detailed description of the invention.
SUMMARY OF THE INVENTION A composition for personal cleansing in the form of a liquid emulsion, which comprises: a) from about 0.1 parts to about 20 parts by weight, of anionic surfactant, b) from about 0.1 parts to about 20 parts by weight, amfoteric surfactant, c) from about 0.5 parts to about 25 parts by weight of a skin moisturizer in the form of an oil, preferably an adduct prepared from vegetable oils containing unconjugated polyunsaturated fatty acid esters, which are conjugated and elaidinized, and then modified by the addition of Diels-Alder, with a member of the group consisting of acrylic acid, fumaric acid and maleic anhydride, d) from about 0. 1 parts to about 2.0 parts of antibacterial agent; e) water, wherein the anionic surfactant and the amphoteric surfactant together comprise from about 0.5 parts to about 30 parts by weight of the composition, and wherein the weight ratio of the anionic surfactant: amphoteric surfactant is within the range from about 1: 5 to about 20: 1.
DETAILED DESCRIPTION OF THE INVENTION The liquid-form cleaners of the present invention are highly preferred first, especially for washing the body, because of their convenience and because they do not soil the sinks or bathrooms. Second, they are antibacterial cleansers for personal use, which kill germs. Third, they are very gentle cleansers for personal use, since they minimize skin irritation, dryness, etc. The personal cleansing compositions of the present invention have these three preferred characteristics, which are very desirable for users of the body cleanser in liquid form. The present invention relates to a personal cleansing composition in the form of a stable liquid emulsion, which comprises: a) from about 0.1 parts to about 20 parts, preferably from 1 part to 15 parts, especially from 3 to 12 parts by weight of anionic surfactant, b) from about 0.1 parts to about 20 parts, preferably from 1 part to 15 parts, especially from 3 to 12 parts by weight, of amphoteric surfactant, c) from about 0.5 part to about 25 parts, preferably from 0.5 parts up to 15 parts, especially from 3 parts to 10 parts by weight, of a skin moisturizer in the form of oil, preferably an adduct prepared from vegetable oils containing esters of unconjugated polyunsaturated fatty acids, which are conjugated and elaidinized and then modified by the addition of Diels-Alder with a member of the group who acrylic acid ester, fumaric acid and maleic anhydride, d) from about 0.1 part to about 2.0 parts of antibacterial agent; e) water, wherein the anionic surfactant and the amphoteric surfactant together comprise from about 0.5 parts to about 30 parts, preferably from 5 parts to 25 parts, especially from 10 parts to 20 parts by weight of the composition, and wherein The weight ratio of the anionic surfactant: amphoteric surfactant, is within the range of from about 1: 5 to about 20: 1, preferably from 1: 2 to about 5: 1, especially from 1: 1 to about 2: 1. The anionic surfactant, is selected from the group consisting of ethoxylated alkyl sulphates, glyceryl alkyl ether sulfonates, acyl methyl taurates, fatty acyl glycinates, N-acyl glutamates, acyl isethionates, alkyl sulfosuccinates, alpha-sulfonated fatty acids, their salts and / or esters, alkyl phosphate esters, ethoxylated alkyl phosphate esters, acyl sarcosinates and fatty acid / protein condensates , and mixtures thereof. The amphoteric surfactant is selected from the group consisting of: (a) imidazolinium derivatives of formula (II)
C2H4OR2
wherein R ^ is C7-C22 alkyl or alkenyl. 2 is hydrogen or CH2Z, each Z is independently or CO2 or CH2CO2M, and M is H, alkali metal, alkaline earth metal, ammonium or alkanolammonium; and / or derivatives of formula (III)
H? H 4
RlCONH (CH2) 2N + CH2Z
R2
wherein R1, R2 and Z, are as defined above: (b) aminoalkanoates of formula (IV)
R1 H (CH2) nC02M and iminodialkanoates of formula (V)
R1N [(CH2) tnC02M] 2
where n and m, are the numbers from 1 to 4, and R < | and M are independently selected from the groups specified in subsection (a) above; and (c) mixtures thereof.
The composition has a viscosity (Brookfield RVT, Bar 5, 50 rpm, 25 ° C temperature), is preferably at least from about 1,000 cps, more preferably from about 2,000 to 1,000,000 cps, especially from about 5,000 to about 7,000 cps, and have an average droplet size of the emulsion of from about 0. 1 to about 40 microns. Preferred compositions have non-Newtonian viscosity characteristics; for example, the preferred compositions have a viscosity (Brookfield RVT, Helipath, Bar T. B, 5 rpm, 25 ° C temperature, for 1 minute), within the range of from about 10,000 to about 40,000 cps, more preferably from about 20,000 to about 30,000 cps.
The essential components are described below, as well as a variety of optional components of the compositions of the present invention.
Ethoxylated Alkyl Sulfate The soft personal cleansing composition in liquid form of the present invention comprises from about 0.1 parts to about 20 parts, preferably from 1 part to 15 parts, especially from 3 parts to 12 parts by weight of an anionic surfactant of alkyl ethoxylated sulfate. The ethoxylated alkyl sulfate surfactants are well known in the art, and can be represented by the formula RO (C2H4?) XS? 3M, wherein R is alkyl or alkenyl of from about 8 to about 24 carbon atoms, x is from 1 to 12, preferably from 2 to 6, and M is a water-soluble cation such as an alkali metal or alkaline earth metal, preferably, sodium, magnesium or potassium. The average degree of ethoxylation, for example the average value of the value for x, must be at least about 2.0. Ethoxylated alkyl sulfates, for example, are condensation products of ethylene oxide and monohydric alcohols, have from about 8 to about 24 carbon atoms. Preferably, R has from about 10 to about 18 carbon atoms. The alcohols can be derived from fats, for example, coconut oil or tallow, or they can be synthetic. Lauryl alcohol and straight chain alcohols derived from coconut oil are preferred in the present application. Said alcohols are normally reactivated with from about 2 to about 12, preferably from about 2 to about 6, more preferably about 3 molar proportions of ethylene oxide and the result of mixing the molecular species having, for example, an average of moles of ethylene oxide per mole of alcohol, is also sulfated and neutralized, within the above limits. Specific examples of the ethoxylated alkyl sulfates, which may be used in the present invention, are especially sodium, magnesium or potassium salts, sulphate glycol triethylene coconut alkyl ethoxylate, sulfate glycol triethylene tallow alkyl ethoxylate, and sulfate hexoxyethylene tallow alkyl. Normally, the alkyl ether sulfates will comprise a mixture of the individual compounds, said mixture preferably having an average alkyl chain length of from about 10 to about 16 carbon atoms, and an average degree of ethoxylation of from about 2 to about about 6 moles of ethylene oxide. Especially preferred are narrow range ethoxylated alkyl sulfates, such as those having ethoxylation levels primarily within the range of from about 2 to about 6.
Amphoteric Surfactant Amphoteric surfactant will be present, in the mild personal cleansing compositions in liquid form of the present invention, at levels of from about 0.1 part to about 20 parts, preferably from 1 part to 15 parts, especially from 3 to 12 parts by weight of the anionic surfactant. The amphoteric component of the present application is selected from the group consisting of amphoteric surfactants of betaine, imidazoline, aminoalkanoate, and iminodialkanoate. Preferably, the proportion of the ethoxylated alkyl surfactant to the amphoteric surfactant will be from about 1: 5 to about 20: 1, more preferably from 1: 2 to about 5: 1, especially, from 1: 1 to about 2: 1. The amphoteric imidazoline surfactants of the present invention are illustrated by Formula I:
R1CON (CH2) nN + -3CH2Z (I) R R2
where R- | it is C8-C22 alkyl or alkenyl. preferably of C12-C16 '• i R2 is hydrogen or CH2CO2M, R3 is CH2CH2OH or CH2CH2OCH2CH2COOM,
R4 is hydrogen, CH2CH2OH, or CH2CH2OCH2CH2COOM, Z is CO2M or CH2CO2M, n is 2 or 3, preferably 2, M is hydrogen or a cation, such as alkali metal or alkaline earth metal. Examples of "alkali metal" include lithium, sodium and potassium. Examples of "alkaline earth metal" include beryllium, magnesium, calcium, strontium, and barium. This type of surfactant is classified by convenience within the present application, as an amphoteric surfactant of "imidazoline", although it must be recognized that it does not necessarily have to be derived, directly or indirectly, through an intermediate imidazoline. Materials of this type that are suitable, are sold under the trade name of MIRANOL, and it is understood that they comprise a complex mixture of species, and can exist in protonated or non-protonated species, depending on the pH, with respect to the species that can have a hydrogen in radical R2. It is understood that all these variations and species are included in the compositions of the present invention. Preferred surfactants of Formula I are monocarboxylated and dicarboxylated. Examples of these materials include cocoamfocarboxipropionate, cocoamfocarboxipropionic acid, cocoamfocarboxiglycinate (which we refer to alternatively as eocoamfodiacetate), and cocoamfoacetate (alternatively, cocoamofomonoacetate). Specific commercial products, which provide the amphoteric surfactant component of the present compositions, include those that are sold under the trade names of MIRANOL C2M CONC N. P., MIRANOL C2M CONC. O.P. , MIRANOL C2M SF, MIRANOL
CM SPECIAL (Miranol, Inc).); ALKATERIC 2CIB (Alkaril Chemicals); AMPHOTERGE W-2 (Lonza, INc); MONATERIC CDX-38, MONATERIC CSH-32 (Mona Industries); REWOTERIC AM-2C (Re o Chemical Group); and SCHERCOTERIC MS-2 (Scher Chemicals). Suitable betaine surfactants of the present application are illustrated by the compounds having the Formula (I I):
OR R4 R2 II I! R5 C-N CH2) m N ^ -Y-Ri (p) R3 wherein: R-1 is a member selected from the group consisting of
COOM and CH-CH S0 M OH
R2 is lower alkyl or hydroxy alkyl; R3 is alkyl or lower hydroxyalkyl; R4 is a member selected from the group consisting of hydrogen and lower alkyl; R5 is higher alkyl or alkenyl; And it is lower alkyl, preferably methyl; m is an integer from 2 to 7, preferably from 2 to 3; n is the integer 1 or 0; M is hydrogen or a cation, such as an alkali metal or alkaline earth metal. The term "lower alkyl" or "hydroxyalkyl" means straight or branched chain, saturated, aliphatic hydrocarbon radicals and substituted hydrocarbon radicals having from one to about three carbon atoms such as, for example, methyl, ethylene, propyl, isopropyl, hydroxypropyl, hydroxyethyl, and the like. The term "higher alkyl or alkenyl" means saturated straight or branched chain (eg, "higher alkyl") and unsaturated (eg, "higher alkenyl"), aliphatic hydrocarbon radicals, having from about 8 to about 20 carbon atoms such as, for example, lauryl, cetyl, stearyl, olel, and the like. Examples of the betaine surfactants of Formula II, which are useful in the present invention, wherein n is zero, include alkylbetaines such as cocodimethylcarboxymethylbetaine, lauryldimethylcaboxymethylbetaine, lauryl dimethyl-alpha-carboxyethylbetaine, cetyldimethylcarboxymethylbetaine, lauryl-bis- ( 2-hydroxyethyl) carboxymethylbetaine, stearyl-bis (2-hydroxypropyl) carboxymethylbetaine, oleydimethyl-gamma-carboxypropylbetaine, lauryl-bis (2-hydroxypropyl) alpha-carboxyethylbetaine) etc. The sulfobetaines may be represented by cocodimethyl sulfopropylbetaine, stearyldimethylsulfopropylbetaine, lauryl bis) 2-hydroxyethyl) sulfopropylbetaine, and the like. The surfactants of betaines amido and betaines amidosulfo which are useful in the present invention, are exemplified by the compounds of Formula II, wherein n is one, but which otherwise correspond to the previous examples. Examples of betaine surfactants of Formula II wherein n is one, which are useful in the present application, include the amidocarboxy-betaines, such as cocoamidodimethylcarboxymethylbetaine, laurylamido-bís (2-hydroxyethyl) -carboxymethylbetaine, cocoamido-bís- (2- hydroxyethyl) -carboxymethylbetaine, etc. The amido sulfobetaines may be represented by cocoamidodimethylsulfopropylbetaine, stearylamidodimethylsulfopropylbetaine, laurylamido-bis- (2-hydroxyethyl) -sulfopropylbetaine, and the like. The preferred betaine in the present invention is a member selected from the group consisting of surfactant of amidocarboxibetains and amidosulfobetaines. The most preferred betaines are the surfactant of amidocarboxibetaines, particularly the cocoamidodimethylcarboxymethylbetaines (cocoamidopropylbetaine), such as those sold by Goldschmidt Co. under the trade name of Tegobetaine (grade F), and by Hoechst-Celanese, under the trade name Genagen CAB. These betaines, which are the most preferred, have the formula:
O CH3 R'3-C-NH- (CH2) 3-N-CH2-COOM CH3
wherein R'3 is selected from alkyl radicals from CQ to C < | 8. and M is hydrogen or a cation, as defined above. In general, the preferred betaines of the present invention will have low levels of the amine residue and sodium monochloroacetate. Suitable aminoalkanoates and iminodialkanoates are represented by Formulas (III) and (IV): aminoalkanoates of the formula:
R-NH (CH2) nCOOM (IB)
iminodialkanoates of the formula:
R-N [(CH 2) mCOOM] 2 C wherein n and m are from 1 to 4, R is C 8 -C 22 alkyl or alkenyl. and M is hydrogen or alkaline, or an alkaline earth metal, as described above. Examples of amphoteric surfactants, which are within the aminoalkanoate formula, include n-alkylamino-propionates and n-alkyliminodipropionates. Said materials are sold by Henkel under the tradename DERIPHAT, and MI RATANE sold by Miranol, Inc. Specific examples include N-lauryl-beta-amino propionic acid or salts thereof, and N-lauryl-beta- acid. amino-dipropionic (DERIPHAT 160C) or salts thereof, and mixtures of the same.
Oil-Shaped Skin Moisturizers Skin-moisturizers in the form of oil will be present in the mild personal cleansing compositions in liquid form of the present application, at levels of from about 0.5 parts to about 25 parts by weight. The term "skin moisturizer in the form of oil," as used in the present application, means any suitable lipid that can be used to moisturize the skin. The skin moisturizer in the form of oil should preferably be an adduct prepared from vegetable oils containing esters of unconjugated polyunsaturated fatty acid, which are conjugated and elaidinized and then modified by the addition of Diels-Alder, with a member of the group consisting of acrylic acid, fumaric acid and maleic anhydride. These adducts and their preparation are described in U.S. Patent No. 4,740,367, issued to Forcé and Associates, April 26, 1988, which is incorporated herein by reference, these adducts being sold under the trade name Ceraphyl. GA (Van Dyke). The preferred vegetable oil adducts are those prepared from soybean oil, and adducts derived by the addition of Diels-Alder from vegetable oils with fumaric acid. A preferred method for the preparation of adducts of the present application is to reactivate two moles of vegetable oil, with a mole of dienophyll in the presence of catalytic amounts of iodine, the conjugation agent and the elaidinizing agent. This produces a 50:50 mixture of an adduct, in conjunction with the disproportionate vegetable oil (conjugate).
Antibacterial Agent The antibacterial agent will be present in the mild personal cleansing compositions in liquid form of the present invention, at levels of from about 0.1 parts to about 1.0 parts. This level is selected in order to provide the desired level of antibacterial activity, and can be modified in any way desired. The preferred antibacterial agent is 2-hydroxy-4,2'4'-trichlorodiphenyl ether (TCS). Other halogenated antibacterial agents are set forth below. Mixtures of these agents can also be used,. Many antibacterial agents may be used, known to those skilled in the art and which are described, for example, in U.S. Patent Nos. 3,835,057 and 4,714,563, which are incorporated herein by reference. Suitable antibacterial agents include: 2-hydroxy-4,2,4'-tpclorodiphenylene ether (TCS); 2,6-dimethyl-4-hydroxychlorobenzene (PCMX); 3,4,4'-trichlorocarbanilide (TCC);
3-trifluoromethyl-4,4'-dichlorocarbanilide (TFC); 2,2'-dihydroxy-3, 3 ', 5, 5', 6,6'-hexachlorodiphenylmethane; 2,2, -dydroxy-3, 3 ', 5,5'-tetrachlorodiphenylmethane; 2,2'-dihydroxy-3,3 ', dibromo-5,5'-dichlorodiphenylmethane; 2-hydroxy-4,4'-dichlorophenyl ether; 2-hydroxy-3,5'-4-tribromodiphenyl ether; and 1-hydroxy-4-methyl-6- (2,4,4-trimethylpentyl) -2 (1 H) -pyridinone (Octopirox). The composition of the present invention is preferably free of Oxeco, phenoxyisopropanol.
Water The mild personal cleansing composition in liquid form of the present invention may also comprise from about 40 parts by weight to about 80 parts by weight of water.
Soft compositions for personal cleansing in liquid form The gentle cleanser for personal cleansing in liquid form of the present invention is substantially free of alkyl sulfate surfactants, since alkyl sulfates are relatively harsh to the skin. It is recognized that some alkyl sulfate will generally be present in said composition, as a result of which it has been present in the raw materials of ethoxylated alkyl sulfate, which are available in the market. For example, the ethoxylated alkyl sulfate (3) available on the market generally contains about 20 parts by weight of alkyl sulfate; the commercially available alkyl ethoxylated sulfate (2) contains from about 25 parts to about 40 parts of alkyl sulfate. For the purposes of the present invention, "substantially free of alkyl sulfate", means that the compositions of the present invention, must have a weight ratio of alkyl sulfate: ethoxylated alkyl sulfate (with an average degree of ethoxylation of 2.5 and as indicated above), not greater than about 0.35, preferably not greater than about 0.30, more preferably not greater than about 0.25. For the ethoxylated alkyl sulfate, with an average level of ethoxylation lower than 2.5, the ratio should not be greater than about 0.40, preferably not greater than 0.35, more preferably not greater than 0.30, still more preferred not greater than 0.25. It is preferable that an additional amount of alkyl sulfate, which is different from that which is inherently in the ethoxylated alkyl sulfate, is not added. In order to reduce the weight ratio of alkyl sulfate: ethoxylated alkyl sulfate, narrow ranges of ethoxylation can be used. "The narrow ranges of ethoxylation" refer to the ethoxylated alkyl sulfate surfactants that have been processed, to reduce the alkyl sulfates and, optionally, the ethoxylated alkyl sulfates which are outside the desired ethoxylation range. The narrow ranges of ethoxylation can be used, reducing the weight ratio of the alkyl sulfate: ethoxylated alkyl sulfate, including such low proportions, as about 0.2, or even about 0.1, and lower. It is also preferred that other ingredients that are unduly harsh to the skin are not added to the mild personal cleansing compositions in liquid form of the present invention.
Additional Ingredients The compositions of the present invention may contain a wide variety of optional ingredients, which are useful or known for use in the art of hand soaps, and other mild compositions for personal cleansing in liquid form. Examples of the additional ingredients are described below. Additional surfactants, which may be used, include other anionic, nonionic and amphoteric surfactants, as well as zwitterionic and cationic surfactants.
Anionic Surfactants A suitable class of anionic surfactants are the water soluble organic salts of the general formula:
*? - S0 -M
wherein R ^ is selected from the group consisting of a straight or branched chain saturated aliphatic hydrocarbon radical having from about 8 to about 24, preferably from about 12 to about 18, carbon atoms; and M is a cation. Important examples are the salts of an organic sulfuric acid reaction product of a hydrocarbon of the methane series, which include iso-, neo-, and n-paraffins, having from about 8 to about 24 carbon atoms, preferably from about 12 to about 18 carbon atoms, and a sulfonation agent, for example, S03. H2SO4, oil, obtained according to the known sulphonation methods, which include bleaching and hydrolysis. The preferred paraffins are the alkali metal paraffins of C-12-C- | 8 sulfonated. Additional examples of anionic surfactants, which are within the conditions of the present invention, are the reaction products of fatty acids esterified with isethionic acid, and neutralized with sodium hydroxide wherein, for example, the fatty acids are derivatives of coconut oil; the potassium salts of methyl tauride fatty acid amides, in which the fatty acids are, for example, coconut oil derivatives. Other anionic synthetic surfactants of this variety are disclosed in U.S. Patent Nos. 2,486,921; 2,486,922; and 2,396,278, which are incorporated herein by reference. Still other ammonium surfactants include the class designated as succinamates. This class includes active surface agents, such as disodium N-octadecylsulfosuccinamate; N- (1,2-dicarboxyethyl) -N-octadecylsulfosuccinamate tetrasodium; diamyl ester of sodium sulfosuccinic acid. Other suitable anionic surfactants usable in the present invention are olefin sulfonates having from about 12 to about 24 carbon atoms. The term "olefin sulfonates", as used in the present application, means compounds of α-olefins which can be produced by sulfonation with simple sulfur trioxide, followed by neutralization of the acid reaction mixture, under such conditions any of the sulfones that have been formed in the reaction, are hydrolyzed to produce the corresponding hydroxy-alkane sulfonates. Sulfur trioxide may be in liquid or gaseous form, and is usually, but not necessarily, diluted by inert diluents, for example, by liquid SO2, chlorinated hydrocarbons, etc. , when they are used in the liquid form; or by air, nitrogen, gaseous SO2, etc. , when they are used in the gaseous form. Another class of anionic surfactants are the b-alkyloxy alkane sulfonates. These compounds have the following formula:
OR2 H I I Rj - C - C - SO3M
H H
where R- | , is a straight chain alkyl group, having from about 6 to about 20 carbon atoms, R 2 is a lower alkyl group having from about 1 (preferably) to about 3 carbon atoms, and M is a water soluble cation . Many additional synthetic anionic surfactants are described in McCutcheon's 1989 Emulsifier and Detergents publication. published by M C. Publishing Co !, which is incorporated herein by reference. Also US Patent No. 3,929,678, issued to Laughlin and Associates, issued December 30, 1975, which is incorporated herein by reference, discloses many other anionic surfactants, as well as other types of surfactants. The soaps, of course, are also within the scope of the anionic detergent surfactants, which can be used. ,
Non-ionic Surfactants A wide variety of non-ionic surfactants can be used. Nonionic surfactants include those broadly defined as compounds produced by the condensation of alkylene oxide groups (hydrophilic in nature), with an organic hydrophobic compound, which may be aliphatic or alkyl of aromatic nature. Examples of the types of nonionic surfactants are: 1. The polyethylene oxide condensates of alkyl phenols, for example, the condensation products of alkyl phenols, having an alkyl group containing from about 6 to about 20 carbon atoms, preferably from about 6 to about 12, in a configuration of , either straight chain or branched chain, with ethylene oxide, said ethylene oxide being present, in equal amounts to from about 10 to about 60 moles of ethylene oxide per mole of alkyl phenol. The alkyl substituent in said compounds can be derived, for example, from polymerized propylene, diisobutylene, octane, or nonane. 2. Those derived from the condensation of ethylene oxide with the product resulting from the reaction of propylene oxide and the ethylene diamine products, which may be of varied composition, depending on the balance desired between the hydrophobic and hydrophilic elements. . For example, compounds containing from about 40 parts to about 80 parts of polydeoxyethylene by weight, and having a molecular weight of from about 5,000 to about 1, 000, resulting from the reaction of ethylene oxide groups are satisfactory. with a hydrophobic base, constituted of the reaction product of the ethylene diamine and the excess of propylene oxide, said base having a molecular weight in the order of cessation of about 2,500, up to about 3,000. 3. The condensation product of the aliphatic alcohols, having from about 8 to about 18 carbon atoms, in a configuration of either straight chain or branched chain, with ethylene oxide, for example a condensate of ethylene oxide of coconut alcohol, has from about 10 to about 30 moles of ethylene oxide per mole of coconut alcohol, the coconut alcohol fraction has from about 10 to about 14 carbon atoms. 4. The long chain tertiary amine oxides correspond to the following general formula: 1 RtR2R3N > OR
wherein Rj contains an alkyl, alkenyl or monohydroxy alkyl radical, of from about 8, to about 18 carbon atoms, from up to about 10 portions of ethylene oxide, and from 0 to about 10 portions of ethylene oxide and from 0 to about 1 glyceryl portion, and R2 and R3 contain from about 1 to about 3 carbon atoms, and from 0 to about 1 hydroxyl group, for example, methyl, ethyl, propyl, hydroxyethyl, or hydroxypropyl radicals. The arrow in the formula is a conventional representation of a semipolar link. Examples of amine oxides suitable for use in the present invention include dimethyl dodecylamine oxide, oleyl di (2-hydroxyethyl) amine oxide, dimethyloctylamine oxide. dimethyl-decylamine oxide, dimethyl-tetradecylamine oxide, 3,6,9-trioxaheptadecyldietylamine oxide, 3-dodecoxy-2-hydroxypropyldi (3-hydroxypropyl) amine oxide, dimethylhexadecylamine oxide. 5. The long chain tertiary phosphine oxides correspond to the following general formula:
RR-R-p > OR
wherein R, contains an alkyl, alkenyl or monohydroxyalkyl radical, within the range of from about 8 to about 18 carbon atoms in the chain length, from or to about 10 portions of ethylene oxide, and from 0 to about 1 glyceryl portion, and R 'and R ", are each alkyl or monohydroxyalkyl groups containing from about 1 to about 3 carbon atoms.The arrow in the formula, is a conventional representation of a semipolar bond. Suitable phosphines are: dodecyldimethylfosphine oxide, tetradecyldimethylphosphine oxide, tetradecylmethylethylphosphine oxide, 3,6,9-trioxaoctadecyldimethylphosphine oxide, cetyl dimethylphosphine oxide, 3-dodecoxy-2-hydroxypropyl oxide (2-hydroxyethyl) L) Phosphine, stearyldimethylphosphine oxide, cetylethylpropylphosphine oxide, oleyldiethylphosphine oxide, dodecyldearylphosphine oxide, tetradecyl oxide diethylphosphine, dodecyldipropylphosphine oxide, dodecyldi (hydroxymethyl) phosphine oxide, dodecyldi (2-hydroxyethyl) phosphine oxide, tetradecylmethyl-2-hydroxypropylphosphine oxide, oleodimethylphosphine oxide, 2-hydroxydedecyldimethylphosphine oxide. 6. The long chain dialkyl sulfoxides contain a short chain alkyl or hydroxyalkyl radical of from about 1 to about 3 carbon atoms (usually methyl), and a hydrophobic long chain including alkyl, alkenyl, hydroxy alkyl radicals, or alkyl, containing from about 8 to about 20 carbon atoms, from 0 to about 10 portions of ethylene oxide, and from 0 to about 1 portion of glyceryl. Examples include: methyl octadecyl sulfoxide, methyl 2-keto tridecyl sulfoxide, 2-hydroxyethyl sulfoxide, methyl dodecyl sulfoxide, 3-hydroxypropyl oleyl sulfoxide, methyl tetradecyl sulfoxide, methyl 3-methoxytridecyl sulfoxide, methyl 3 sulfoxide. -hydroxytridryl, methyl 3-hydroxy-4-dodecoxybutyl sulfoxide. 7. Polysorbates, for example, sucrose esters of fatty acids. Such materials are described in US Pat. No. 3,480,616, for example sucrose cocoate (a mixture of sucrose esters of a coconut acid, consisting mainly of monoesters, and sold under the trade names of RITA GRILLOTEN LSE 87K, and CRODESTA
SL-40 of Croda). 8. Non-ionic alkyl polysaccharide surfactants are described in U.S. Patent No. 4,565,647, issued to Llenado, issued January 21, 1986, having a hydrophobic group containing from about 6 to about 30 carbon atoms, preferably from about 10 to about 16 carbon atoms, and a polysaccharide, for example, a hydrophilic group, polyglycoside. The polysaccharide may contain from about 1.0 to about 10, preferably from about 1.3 to about 3, more preferably from about 1.3 to about 2.7 saccharide units. It can be used, any reductive saccharide, containing 5 or 6 carbon atoms for example, portions of glucose, galactose and galactosyl, can be substituted for the glucosyl portions. (Optionally, the hydrophobic group is adhered in the 2-, 3-, 4-, etc. positions, therefore, they produce a glucose or galactose in the opposite way to a glycoside or galactoside). The links between the saccharide can be, for example, between the position one of the additional saccharide units, and the positions 2-, 3-, 4-, and / or 6-, in the preceding saccharide units. Optionally less desirable, there may be a polyalkylene oxide chain linking the hydrophobic portion and the polysaccharide portion. The preferred alkylene oxide is ethylene oxide. Typical hydrophobic groups include alkyl groups, either saturated or unsaturated, branched or unbranched, containing from about 8 to about 18, preferably from about 10 to about 16 carbon atoms. Preferably, the alkyl group is a saturated straight-chain alkyl group. The alkyl group may contain up to about 3 hydroxyl groups and / or the polyalkylene oxide chain may contain up to about 10, preferably less than 5, alkylene portions. Suitable alkyl polysaccharides are octyl, nonyldecyl, undecyldecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, and octadecyl, di-, tri-, tetra-, penta-, and hexaglucosides, galactosides, lactosides, glucoses, fructosides, fructose and / or galactoses. Suitable mixtures include coconut alkyl, di-, tri-, tetra-, and pentaglucosides and tetra-, penta-, and tallow alkyl glycosides. 9. The fatty esters glycer? >or polyethylene glycol (PEG), as described in the formula RC (0) OCH2CH (OH) CH2 (OCH2CH2) nOH, wherein n is from about 5 to about 200, preferably from about 20 to about 100, more preferably from about 30 to about 85, and RC (O) - is an ester, wherein R comprises an aliphatic radical having from about 7 to 19 carbon atoms, preferably from about 9 to 17 carbon atoms, more preferably from about 1 1 to 17 carbon atoms, still more preferably, about 1 1 to 14 carbon atoms. Preferred are combinations of n from about 20 to about 100, with fatty esters of C - | 2 ~ C - | 8 preferably of C 12-C 1 5. to minimize the adverse effect on foam generation. Suitable glyceryl fatty ester portions of these surfactants include fatty esters of glyceryl cocoate, seboato glyceryl, glyceryl palmate, glyceryl stearate, glyceryl laurate, glyceryl oleate, glyceryl ricinoleate, and glyceryl derivatives. of triglycerides, such as palm oil, almond oil, and corn oil. Other surfactants that may be used include soluble cationic surfactants, such as quaternary ammonium surfactants, and other amphoteric and zwitterionic surfactants known to those skilled in the art.
Derivatives of Cationic Cellulose Ether The mild personal cleansing compositions in the form of the present invention may comprise a cationic cellulose ether derivative. The cationic cellulose ether derivatives, for the purposes of the present invention, are a quaternary ammonium salt of hydroxyethyl cellulose, reactivated with a substituted trimethyl ammonium epoxide. The foam generation enhancers are well known in the art. Polyquaternium-10 (an industrial term designated by the Cosmetic, Toiletry and Fragrance Association (CFTA)), for a polymeric quaternary ammonium salt of reactive hydroxyethyl cellulose with a substituted epoxide of trimethyl ammonium, is a preferred polymer to improve generation of foam. Polyquaternium-10, is marketed by Union Carbide Corp. (Danbury, Connecticut, USA), under its series of materials UCARE POLYMER JR, for example, UCARE POLIMER JR-30M, JR-125, and JR400.
Conditioning Agents Another component, including the addition of Vaseline. Vaseline may be any white or yellow petroleum jelly, recognized in the art as being suitable for human application. The preferred type is USP Class I II, with a melting point at a temperature between 122 and 175 ° F (50 and 57 ° C). Said material is marketed by Penreco Snow White Pet USP. The petrolatum in the present invention includes hydrocarbon mixtures, formulated with mineral oils in combination with paraffin waxes of various melting points. Preferred conditioning agents of this type are described in U.S. Patent Application Serial No. 07 / 909,834, issued to Dias y Asociados, issued on July 7, 1992, and U.S. Patent Application Serial No. 07 / 909,877 , granted to Kacher y Asociados, issued on July 7, 1992, which are mentioned with permission and incorporated into the present description, as a reference. Examples of other humectants include water-soluble hexadecyl, myristyl, isodecyl or isopropyl esters of adipic, oleic, stearic, myristic or linoleic acids, as well as many other corresponding alcohol esters (sodium isostearoyl-2-lactylate, caprylate lactylate) sodium), polyethylene glycol esters, such as caprylic glycerate / capric PEG (6) (Softigan 767), hydrolyzed protein, and other proteins derived from collagen, aloe vera gel and acetamide MEA. An optional component of the compositions of the present invention is a soluble conditioning agent suitable for conditioning the hair or skin. It can also be used, the proteolytic enzyme conditioning of the skin. Suitable conditioners include, for example, soluble polyether siloxane copolymer, such as: modified dimethylpolysiloxane with propylene oxide (e.g., Dow Corning DC-1248), however, ethylene oxide and mixtures of ethylene oxide and propylene oxide can be used. The level of ethylene oxide and polypropylene oxide should be high enough to provide solubility in water and the composition thereof.
Other Optional Components The skin cleansers of the present invention may contain a variety of optional, non-essential ingredients suitable for improving said compositions in a variety of ways. Such optional, conventional ingredients are well known to those skilled in the art. art, for example, preservatives, such as Hidantoin HMDM, benzyl alcohol, methyl paraben, propyl paraben, 3-isothiazolines (Kathon CG marketed by Rohm and Haas), imidazolidinyl urea, methylchloroisothiazolinone, and methylsothiazolinone, can be used in amounts of 1 up to 5,000 ppm; thickeners and viscosity modifiers, such as sodium sulfate, polyethylene glycols, sodium chloride, ammonium chloride, carboxymethylcellulose, methylcellulose, polyvinyl alcohol, and ethyl alcohol; suspending agents such as magnesium / aluminum silicate; perfumes, dyes; opacifiers, such as ethylene glycol distearate, glycol monostearate, styrene acrylate copolymer, mica, behenic acid, and calcium stearate; sequestering agents, such as disodium ethylenediamine tetraacetate; emollients, humectants and various other ingredients for the treatment of the skin, such as glycerin; regulators and accumulators, such as citrates and phosphates. If they are present, said agents individually, generally comprise from about 0.01 parts to about 5 parts by weight of the composition.
Implements A pad or sponge for the body, which is made of nylon mesh, in the form of a round sponge (approximately 4.5 in diameter), which when used in conjunction with the present invention, is an effective system, which improves the proportion of a gentle cleansing for the skin, and beneficial conditioners for the skin. This pad is made by the sponge factory (Bilange) The pad is composed of three pieces of extruded tubular mesh, which is folded several times to form a soft sponge shaped balloon, with a nylon rope attached.
METHOD OF USE In its aspect of the method of use, the present invention comprises a method for washing the skin by contacting the skin with an amount of the cleaning compositions of the present invention, which are effective for cleaning the skin, and Rinse off excess skin cleanser. An effective amount for any individual will depend on variable factors such as the amount of dirt on the skin, the type of dirt on the skin, the level of surfactant in the cleaning composition, etc. Generally, an effective amount will be from about 0.5 to about 5 grams per application.
EXAMPLES The present invention is illustrated by the following examples, which are not limiting thereof. In the examples, all concentrations are on active bases of 100 parts, and the abbreviations have the following meanings: Anionic Sulfate Laurite 3.6 Sodium Magnesium Amfoteric 1 Lauroamfoacetate Sodium Amphoteric 2 Betaine Cocamidopropyl Nonionic Cocamide MEA Oil 1 Bean Oil Soybean Handling Oil 2 Soybean Oil Polyquaternum Polymer - 10 Antibacterial 1 Triclosan Antibacterial 2 Triclocarban Preservative Hidantoin DMDM Thickener 1 Fatty Acid Palm Pulp Thickener 2 Magnesium Sulfate Glyceride Celoric / Capric Glycerides Peg 6
Examples from I to VI The following are compositions for personal cleansing in the form of products with foam generation for the bath, and which are representative of the present invention:
I II III IV V Anionic 1 0.0 1 2.0 12.0 12.0 10.0 12.0 Amfoteric 1 5.0 6.0 - - 5.0 6.0 Amfoteric 2 - - 6.0 6.0 Non-ionic 2.8 2.8 2.8 2.8 2.8 2.8 Oil 1 2.0 2.0 2.0 2.0 2.0 2.0 Oil 2 8.0 8.0 8.0 8.0 8.0 8.0 Glycerin 3.0 3.0 3.0 3.0 3.0 3.0 Polymer 0.4 0.4 0.4 0.4 0.4 0.4 Antibacterial 1 0.3 0.3 0.3 - Antibacterial 2 - - - 0.7 0.7 0.7 Preservative 0.2 0.2 0.2 0.2 0.2 0.2 Thickener 1 1 .9 1 .9 1 .9 1 .9 1 .9 1 .9 Thickener 2 0.1 0.1 0.1 0. 1 0. 1 0.1 Glycerides 4.0 4.0 4.0 4.0 4.0 4.0 Fragrance 1 .0 1 .0 1 .0 1 .0 1 .0 1 .0 Water up to 100
The liquid cleaners above are the most preferred first, because they are special to be used as body cleansers, due to their convenience and that they do not soil the sink or bathroom. Secondly, they are antibacterial cleansers for personal use, which kill germs. Third, they are very gentle cleansers for personal use, since they minimize skin irritation, dryness, etc. These compositions for personal cleansing have three of these preferred characteristics, which are very desired by the users of body cleansers in liquid form. The example I I is the most preferred for its generation of foam.
Claims (5)
1.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US37007395A | 1995-01-09 | 1995-01-09 | |
| US370073 | 1995-01-09 | ||
| PCT/US1996/000213 WO1996021426A1 (en) | 1995-01-09 | 1996-01-05 | Three in one ultra mild lathering antibacterial liquid personal cleansing composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MX9705154A MX9705154A (en) | 1997-10-31 |
| MXPA97005154A true MXPA97005154A (en) | 1998-07-03 |
Family
ID=
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