EP0521980A1 - Novel surfactants and surfactant compositions - Google Patents
Novel surfactants and surfactant compositionsInfo
- Publication number
- EP0521980A1 EP0521980A1 EP91906853A EP91906853A EP0521980A1 EP 0521980 A1 EP0521980 A1 EP 0521980A1 EP 91906853 A EP91906853 A EP 91906853A EP 91906853 A EP91906853 A EP 91906853A EP 0521980 A1 EP0521980 A1 EP 0521980A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- group
- alkylene
- diamine
- carbon atoms
- ammonium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0094—High foaming compositions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/11—Esters of phosphoric acids with hydroxyalkyl compounds without further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/34—Derivatives of acids of phosphorus
- C11D1/345—Phosphates or phosphites
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/30—Amines; Substituted amines ; Quaternized amines
Definitions
- the present invention relates to novel low skin irritation surfactants and surfactant compositions which are high in foaming properties containing, as an active ingredient, a diamine monoalkyl phosphate salt.
- Soaps, detergents and abrasives have long been used to cleanse the skin on various portions of the body.
- Anionic surfactants such as alkyl sulfates, polyoxyethylene alkyl sulfates, alkylbenzene sulfon- ates and ⁇ -olefin sulfonates have been widely used as the surfactant component for many cleansers.
- Nonionic surfactants cause little or no skin dryness or roughness. However, they do not have the same advantageous properties of foaming and detergency as anionic surfactants. It has, therefore, not been suitable to incorporate nonionic surfactants into cleansing compositions as the primary detergent component.
- Phosphoric add esters have been known as anionic surfactants, generally as mono- and diesters, or mixtures thereof. However, in general, their water solubilities and foaming properties are not very good.
- European Patent No. 265 702 published Hay 4, 1988 discloses transparent or semi-transparent cosmetic compositions containing a monoalkyl phosphate, water, oil and alcohol for skin treatment. The oils and alcohols are used to obtain clarity.
- U.S. Patent 4,573,749 to Mclntosh, issued June 28, 1988 discloses monoamine alkyl phosphates having antimicrobial activity.
- U.S. Patent 4,290,904 to Poper et al., issued September 22, 1981, U.K. Patent No. 1,513,053, published June 7, 1978 and European Patent 023 978, published February 18, 1981 disclose cosmetic and toiletry preparations containing alkoxylated alkylene diamines.
- Patent 4,476,043, 4,476,044 and 4,476,045 to O'Lenlck all Issued October 9, 1984 and U.S. Patent 4,477,372 to O'Lenick, issued October 16, 1984 disclose substantially non-aqueous surfactants containing an organic sulfate, mineral oil and an alkoxyl- ated amine.
- Patent 4,477,372 to O'Lenick issued October 16, 1984 disclose substantially non-aqueous surfactants containing an organic sulfate, mineral oil and an alkoxyl- ated amine.
- none of these references disclose the use of a diamine alkyl phosphate surfactant.
- Monoalkyl phosphate salts have also been disclosed as useful surfactants in U.S. Patent 4,139,485 to Imokawa et al., issued February 13, 1979.
- these surfactants form turbid aqueous solutions unless they contain other solvents (e.g., solubilizing agents).
- solvents e.g., solubilizing agents.
- the rheology of these salts limits the variety of formulations which can be made with aesthetically pleasing characteristics.
- One of the principal purposes of this invention is to describe the preparation of an aqueous skin cleansing composition made from the novel diamine monoalkyl phosphate salts of the present invention which will produce a usable foam from a hand-held, squeezable foam dispensing device, as well as from an aerosol device and further which will not render the device unusable by, for example, clogging the device.
- Another object of this invention is to provide surfactants and foam-producing surfactant compositions which produce relatively stable or collapsible foams.
- a preferred embodiment of this invention is to provide skin cleansing foams of low density.
- Another object of this invention is to provide surfactants and foaming compositions with creamy lather, good skin feel and good rinsability and which retains skin elasticity.
- R is a hydrophobic group or the condensation product of a hydrophobic group with ethylene oxide, preferably R is alkyl or alkenyl having an average of from about 10 to 18 carbon atoms
- X 1 and X 2 are independently selected from the group consisting of hydrogen, alkali metal, ammonium, substituted ammonium (e.g., alkoxylated ammonium, alkylammonium, alkoxylated aliphatic amines, polyethoxylated amines) and alkylene diamine, provided that at least one of X 1 and X 2 is a totally hydroxyalkylatad alkylene diamine.
- compositions comprising these diamine monoalkyl phosphate salts.
- Sesquialkyl phosphate salts are not within the scope of the present invention.
- the surfactant compounds of the present invention are of the formula:
- R is a hydrophobic group or the condensation product of a hydrophobic group with ethylene oxide, preferably R is alkyl or alkenyl having an average of from about 10 to 18 carbon atoms
- X 1 and X 2 are independently selected from the group consisting of hydrogen, alkali metal, ammonium, substituted ammonium (e.g., alkoxylated ammonium, alkylammonium, alkoxylated aliphatic amines, polyethoxylated amines) and alkylene diamine, provided that at least one of X 1 and X 2 is a totally hydroxy alkylatedalkylene diamine.
- Monoalkyl phosphate salts in the present invention can be prepared, for example, by a known process wherein a long chain aliphatic alcohol (or the condensation product of a long chain aliphatic alcohol with ethylene oxide) is reacted with a phosphatizing agent such as phosphoric anhydride or phosphorus oxychloride. It is recognized that the dialkyl phosphate can be by-produced by this process and which possess poor water-solubility or foaming properties. Such dialkyl phosphates have the formula:
- R is a hydrophobic group or the condensation product of a hydrophobic group with ethylene oxide, preferably R is alkyl or alkenyl having an average of from about 10 to 18 carbon atoms, and wherein X 3 is selected from the group consisting of hydrogen, alkali metal, ammonium, substituted ammonium (e.g., alkoxylated ammonium, alkylammonium, alkoxylated aliphatic amines, polyethoxylated amines) and alkylene diamine.
- R is the condensation product of a hydrophobic group with from about 1 to about 10 moles and preferably from about 1 to about 4 moles of ethylene oxide.
- the weight ratio of the diamine monoalkyl phosphate salt to the dialkyl phosphate salt is from about 99:1 to about 70:30, respectively, preferably from about 100:0 to about 90:10, most preferred is a ratio of substantially 100:0.
- these diamine phosphates of the diester are uniquely water-soluble and, therefore, will not interfere as much with the devices and formulations described herein.
- the surfactants of the present invention are particularly useful in detergent products which are directly contacted with the skin for a long time such as facial cleansers, shampoos, and solid synthetic detergent toilet bars, because they have a characteristic, excellent foaming power and skin roughness is not caused.
- the surfactants can also be used as ingredients of dish-washing liquid detergents, powder detergents and dentifrices and are particularly useful compositions where a clear and non-turbid composition is desirable.
- the saturated and unsaturated hydrocarbon groups having an average carbon number of 10-18 (R) are straight chain, branched or allcycllc hydrocarbons such as decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, and octadecyl groups and corresponding olefinically unsaturated groups.
- Those hydrocarbon groups are contained in the compositions singly or in the form of a combination of several groups.
- Saturated hydrocarbon groups of an average carbon number of 10 to 14 and unsaturated hydrocarbon groups of an average carbon number of 16 are particularly preferred.
- the saturated or unsaturated hydrocarbon groups wherein said hydrocarbon groups possess from about 1 to about 10 units and preferably from about 1 to about 4 units of ethylene oxide per molecule.
- the preferred alkali metals for X 1 and X 2 according to the invention are, for example, lithium, sodium and potassium.
- the alkylammonium or substituted alkylammonium for X 1 and X 2 according to the invention are cations produced from amines used for neutralization of the corresponding phosphoric acids by salt formation after the neutralization step in the process for preparing monoalkyl phosphate salts in the present invention.
- the corresponding amines are primary, secondary and tertiary amines having alkyl groups of 1 to 4 carbon atoms which can be further substituted, particularly by hydroxyl groups.
- amines there can be mentioned, for example, d1methylmonoethanolamine, methyldlethanol amine, trimethyl amine, triethylamine, d1butylamine, butyldimethylamine, monoethanol ami ne, diethanolamine, triethanolamine, isopropyldimethylamine and isopropyl- ethanolamine.
- Preferred amines are monoethanolamine, diethanolamine and triethanolamine.
- a particularly preferred amine is triethanolamine.
- amines include arginine, lysine, mono-, di- or triisopropanolamine, N,N-tris(hydroxymethyl)aminomethane, diglycol- amine, glucamine, arainomethylpropanol, and aminomethylpropanediol.
- the alkylene diamine, according to the present invention has the general formula:
- R 1 , R 2 , R 4 and R 5 are independently hydrogen, an alkyl group having 1 to 4 carbon atoms or a hydroxylal kyl or dihydroxyalkyl group having 1 to 4 carbon atoms or R 4 and R 5 jointly form a saturated 5 or 6 membered heterocyclic ring, which can be substituted by an oxo- or hydroxyalkyl group and R 3 represents an alkylene or hydroxyalkylene group having 2 to 4 carbon atoms, provided that at least one of R 1 , R 2 , R 3 , R 4 and R 5 contain at least one hydroxy group.
- a particular amine class that is useful herein is an N,N-tetrakis (hydroxyalkyl) ethylene diamine having the formula:
- R 1 is alkylene having two to four carbon atoms
- R is hydrogen or an alkyl group having one to six carbon atoms
- n is from one to four.
- the foregoing diamine preferably has a molecular weight of under about 1700, preferably under about 1200, even more preferably under about 800 and most preferably under about 500.
- the tetrakis (hydroxyalkyl) ethylene diamine is best exemplified by the compound N,N,N',N'-tetrakis(2-hydroxypropyl)-ethylenediamine, obtainable commercially under the trademark Quadrol or Neutrol TE (both available from BASF Wyandotte Company).
- diamine monoalkyl phosphate salts useful in the present invention include, but are not limited to,
- compositions of the present invention comprise:
- compositions comprise a mixture of the diamine monoalkyl phosphate salts wherein R is selected from the group consisting of C 12 to C 14 alkyl or alkenyl and C 16 to C 18 alkyl or alkenyl (or the condensation porduct of these moieties with from about 1 to about 10 moles of ethylene oxide) and wherein said salts are present in a ratio of from about 80:20 to about 20:80, preferably from about 60:40 to about 40:60 and most preferably from about 55:45 to about 45:55, respectively.
- compositions of the present invention can be administered topically, i.e., by the direct laying on or spreading of the composition on epidermal or epithelial tissue.
- Such compositions can be formulated as foams, lotions, creams, ointments, solutions, gels or solids.
- a highly preferred composition contains the monoalkyl phosphate salt in a soap matrix (i.e., liquid and solid).
- These topical compositions comprise a safe and effective amount, usually from about 0.1% to about 99%, and preferably from about 1% to about 10%, of the monoalkyl phosphate salt.
- Bar compositions generally contain very high levels I.e., above 80%, of the diamine monoalkyl phosphate salt.
- the carrier is either organic in nature or a solution or an aqueous emulsion and is capable of having the diamine monoalkyl phosphate salt dispersed, dissolved or suspended therein.
- the carrier can include pharmaceutically-acceptable emollients, skin penetration enhancers, coloring agents, fragrances, emulsifiers, thickening agents, and solvents.
- the lotions can comprise a safe and effective amount of the monoalkyl phosphate salt; from about 0.1% to about 25%, preferably from about 3% to about 15%, of an emollient; the balance being water, a C 2 or C 3 alcohol, or a mixture of water and the alcohol.
- suitable emollients are as follows:
- Hydrocarbon oils and waxes examples are mineral oil, petrolatum, paraffin, ceresin, ozokerite, microcrystalline wax, polyethylene, and perhydrosqualane.
- Silicone oils such as polydimethylsiloxanes, methylphenyl- polyslloxanes, water-soluble and alcohol-soluble silicone-glycol copolymers.
- Triglyceride fats and oils such as those derived from vegetable, animal and marine sources. Examples include castor oil, safflower oil, cotton seed oil, corn oil, olive oil, cod liver oil, almond oil, avocado oil, palm oil, sesame oil, and soybean oil.
- Acetoglyceride esters such as acetylated monoglycerides.
- Ethoxylated glycerides such as ethoxylated glyceryl mono- stearate.
- Alkenyl esters of fatty acids having 10 to 20 carbon atoms examples thereof include oleyl myristate, oleyl stearate, and oleyl oleate.
- Fatty adds having 9 to 22 carbon atoms Suitable examples include pelargonlc, laurlc, myristic, palmitic, stearic, isostearic, hydroxystearic, oleic, linoleic, ricinoleic, arachldonic, behenic, and erudc acids.
- Fatty alcohols having 10 to 22 carbon atoms Lauryl, myristyl, cetyl, hexadecyl, stearyl, isostearyl, hydroxystearyl, oleyl, ricinoleyl, behenyl, erucyl, and 2-octyl dodecyl alcohols are examples of suitable fatty alcohols.
- Ethoxylated fatty alcohols of 10 to 20 carbon atoms include the lauryl, cetyl, stearyl, isostearyl, oleyl, and cholesterol alcohols having attached thereto from 1 to 50 ethylene oxide groups or 1 to 50 propylene oxide groups, or a mixture thereof.
- Ether-esters such as fatty acid esters of ethoxylated fatty alcohols.
- Lanolin and its derivatives Lanolin, lanolin oil, lanolin wax, lanolin alcohols, lanolin fatty acids, isopropyl lanolate, ethoxylated lanolin, ethoxylated lanolin alcohols, ethoxylated cholesterol, propoxylated lanolin alcohols, acetylated lanolin, acetylated lanolin alcohols, lanolin alcohols linoleate, lanolin alcohols ricinoleate, acetate of lanolin alcohols ricinoleate, acetate of ethoxylated alcohols-esters, hydrogenolysis of lanolin, ethoxylated hydrogenated lanolin, ethoxylated sorbitol lanolin, and liquid and semisolid lanolin absorption bases are illustrative of emollients derived from lanolin.
- Polyhydrlc alcohols and polyether derivatives Propylene glycol, dipropylene glycol, polypropylene glycol (M.W. 2000-4000), polyoxyethylene polyoxypropylene glycols, polyoxypropylene polyoxyethylene glycols, glycerol, ethoxylated glycerol, propoxylated glycerol, sorbitol, ethoxylated sorbitol, hydroxypropyl sorbitol, polyethylene glycol (M.H. 200-6000), methoxy polyethylene glycols, polyethylene oxide] homopolymers (M.W.
- polyalkylene glycols and derivatives examples thereof.
- hexylene glycol (2-methyl-2,4-pentanediol)
- 1,3-butylene glycol 1,2,6-hexanetriol
- ethohexadiol USP (2-ethyl1,3-hexanediol)
- C 15 -C 18 vicinal glycol examples thereof.
- Ethylene glycol mono- and di-fatty acid esters diethylene glycol mono- and di-fatty acid esters, polyethylene glycol (M.W. 200-6000) mono- and di-fatty acid esters, propylene glycol mono- and di -fatty acid esters, polypropylene glycol 2000 monooleate, polypropylene glycol 2000 mo ⁇ ostearate, ethoxylated propylene propylene glycol monostearate, glyceryl mono- and di-fatty add esters, polyglycerol poly-fatty acid esters, ethoxylated gylceryl monostearate, 1,3-butylene glycol monostearate, 1,3-butylene glycol distearate, polyoxyethylene polyol fatty acid ester, sorbitan fatty acid esters, and polyoxyethylene sorbitan fatty acid esters are satisfactory polyhydric alcohol esters.
- Wax esters such as beeswax, spermaceti, myristyl myristate, stearyl stearate.
- Beeswax derivatives e.g., polyoxyethylene sorbitol beeswax. These are reaction products of beeswax with ethoxylated sorbitol of varying ethylene oxide content, forming a mixture of ether-esters.
- Vegetable waxes including carnauba and candelilla waxes.
- Phospholipids such as lecithin and derivatives.
- Sterols Cholesterol, cholesterol fatty acid esters are examples thereof.
- Amides such as fatty acid amides, ethoxylated fatty acid amides, solid fatty acid alkanolamides.
- the lotions further comprise from about 1% to about 10%, preferably from about 2% to about 5%, of an emulsifler.
- the emulsifiers can be nonionic, anionic or cationic. Examples of satisfactory nonionic emulsifiers include fatty acid alcohols having 10 to 20 carbon atoms, fatty alcohols having 10 to 20 carbon atoms condensed with 2 to 20 moles of ethylene oxide or propylene oxide, alkyl phenols with 6 to 12 carbon atoms in the alkyl chain condensed with 2 to 20 moles of ethylene oxide, mono- and di-fatty acid esters of ethylene oxide, mono- and di-fatty add esters of ethylene glycol wherein the fatty add moiety contains from 10 to 20 carbon atoms, diethylene glycol, polyethylene glycols of molecular weight 200 to 6000, propylene glycols of molecular weight 200 to 3000, glycerol, sorbitol, sorbitan, polyoxyethylene sorbitol
- Suitable anionic emulsifiers include the fatty acid soaps, e.g. sodium, potassium and triethanolamine soaps, wherein the fatty acid moiety contains from 10 to 20 carbon atoms.
- Other suitable anionic emulsifiers include the akali metal, ammonium or substituted ammonium alkyl sulfates, alkyl arylsulfonates, and alkyl ethoxy ether sulfonates having 10 to 30 carbon atoms in the alkyl moiety.
- the alkyl ethoxy ether sulfonates contain from 1 to 50 ethylene oxide units.
- anionic emulsifiers can result in a turbid formulation, and hence, anionic emulsifiers are less preferred for use herein.
- the balance of the lotion is water or a C 2 or C 3 alcohol, or a mixture of water and the alcohol.
- the lotions are formulated by simply admixing all of the components together.
- Preferably the monoalkyl phosphate salt is dissolved in the mixture.
- Conventional optional components can be included.
- One such additive is a thickening agent at a level from about 1% to about 10% of the composition.
- suitable thickening agents include: cross-linked carboxy- polymethylene polymers (sufficiently neutralized), magnesium aluminum silicate, carboxymethylcellulose, hydroxyethylcellulose, acrylic acid polymers (e.g.
- Cationic polymers such as cationic guar gum, are not preferred for use herein.
- compositions of the present invention also can be formulated in a cream form.
- the creams comprise safe and effective amounts of the monoalkyl phosphate salt; from about 0.1% to 95%, preferably from about 10% to about 25%, of an emollient; the balance being water.
- the emollients above described can also be used in the cream compositions .
- the cream form contains a suitable emulsifler, as previously described. When an emulsifler is included, it is the composition at a level from about 3% to about 50%, preferably from about 5% to about 20%.
- compositions of this invention can also be formulated as a solution.
- the solution form comprises a safe and effective amount of the monoalkyl phosphate salt, usually at least about 0.01% up to about 50% and preferably about 0.1% to about 10%; the balance being water or a suitable organic solvent.
- Suitable organic materials useful as the solvent or a part of a solvent system are as follows: propylene glycol, polyethylene glycol (M.W. 200-1000), polypropylene glycol (M.W. 425-2025), butylene glycol, glycerine, sorbitol esters, 1,2,6- hexanetriol, ethanol, isopropanol, diethyl tartrate, butanediol, and mixtures thereof.
- aerosol compositions further comprise from about 25% to about 80%, preferably from about 30% to about 50%, of suitable propellants.
- suitable propellants are the chlorinated, fluorinated and chlorofluorinated lower molecular weight hydrocarbons. Nitrous oxide, carbon dioxide, butane, and propane can also be used as propellant gases. These propellants are used at a level sufficient to expel the contents of the container.
- the above containers do not use any propellant and are therefore safe for the consumer and the environment. They create a foam from almost any surfactant composition. Although there is no need to add foam boosters merely for the purpose of stabilizing the foam, such materials can be desirable. In some compositions the use of foam boosters can even be counterproductive since the foam has to break in order for the container to work properly.
- the composition is placed in the container reservoir (plastic squeeze bottle). Squeezing the container with the hand forces the composition through a foamer head, or other foam producing means, where the composition is mixed with air and then through a homogenizing means that makes the foam more homogeneous and controls the consistency of the foam. The foam i s then di scharged as a uniform, non-pressurized aerated foam.
- the minimum pressure to activate the squeeze foamer is about 1 psig, typically from about 2 psig to about 7 psig.
- the minimum pressure is related to the size of the channels in the dispenser, the viscosity of the composition, etc.
- the density of the foam should be between about 0.002 and about 0.25 g/cc, preferably between about 0.01 and about 0.12 g/cc, and more preferably between about 0.02 and about 0.07 g/cc.
- the carrier liquid in a mouthwash is generally a mixture of ethanol and water.
- the amount of ethanol is generally from about 5% to about 60%, preferably from about 5% to about 25% by weight of the carrier. Water then constitutes the remainder of the carrier liquid mixture.
- These mouthwash compositions can also contain other optional components such as emulsifying agents as previously described, flavoring agents, sweeteners, and humectants.
- Other mouthwash formulations and methods for making mouthwashes useful in the present invention are disclosed in U.S. Patent 4,323,551 to Parran, issued April 6, 1982 , which i s incorporated by reference herein.
- compositions herein can be formulated into a gel form by simply admixing a suitable thickening agent to the previously described solution compositions.
- suitable thickening agents have been previously described with respect to the lotions.
- the gelled compositions comprise a safe and effective amount of the monoalkyl phosphate salt, from about 0.5% to about 20%, preferablly from about 1% to about 10%, of the thickening agent; the balance being water.
- compositions of this invention can also be formulated in a solid form, e.g., a stick-type composition.
- Such compositions comprise a safe and effective amount of the monoalkyl phosphate salt and from about 0.01% to about 99%, preferably from about 60% to about 90%, of the previously described emollients.
- This composition can further comprise from about 0.1% to about 20%, preferably from about 5% to about 15%, of a suitable thickening agent, and optionally emulsifiers and water. Thickening agents previously described with respect to lotions are also suitable herein.
- compositions of this invention can also be formulated into a liquid or solid (e.g., bar) soap matrix.
- Such compositions comprise a safe and effective amount of the monoalkyl phosphate salt ranging from about 0.1% to about 99%; and from about 1% to about 99% of an excipient such as those previously described.
- the soap contains a suitable emulsifier as previously described. When an emulsifier is included, it is in the composition at a level from about 10% to about 50%. 7. Dentifrices.
- compositions of this invention can also be formulated as dentifrices.
- dentifrices especially toothpaste, comprise a safe and effective amount of the monoalkyl phosphate salt ranging from about 0.1% to about 20% by weight of the composition.
- Toothpaste compositions conventionally contain abrasive materials, sudsing agents, binders, humectants, flavoring and sweetening agents. Suitable dentifrice compositions and the methods of their manufacture useful in the present invention are fully set forth in U.S. Patent 3,535,421 to Briner et al., issued October 20, 1970, which is incorporated by reference herein.
- compositions of this invention also can be formulated in a shampoo form.
- the shampoos comprise a safe and effective amount of the diamine monoalkyl phosphate salt ranging from about 0.1% to about 99%; from about 5% to about 60% of a synthetic surfactant; and the balance water.
- a secondary surfactant can also be utilized, however, such secondary surfactant should be neutralized by a diamine as described above.
- These shampoos can contain a variety of nonessential optional components.
- Such conventional optional ingredients are well known to those skilled in the art, e.g., preservatives, such as benzyl alcohol, ethyl paraben, propyl paraben and imidazolidinyl urea; cationic surfactants, such as cetyl trimethyl ammonium chloride, stearyldimethyl benzyl ammonium chloride, and di (partially hydrogenated tallow) dimethylammonium chloride; thickeners and viscosity modifiers such as diethanolamide of a long-chain fatty acid (e.g.
- PEG 3 lauramide block polymers of ethylene oxide and propylene oxide, sodium chloride, sodium sulfate, polyvinyl alcohol, and ethyl alcohol; pH adjusting agents, such as dtric acid, succinic acid, phosphoric acid, sodium carbonate; perfumes; dyes; and, sequestering agents, such as disodium ethylenediamine tetraacetate.
- pH adjusting agents such as dtric acid, succinic acid, phosphoric acid, sodium carbonate
- perfumes dyes
- sequestering agents such as disodium ethylenediamine tetraacetate.
- Such agents generally are used individually at a level of from about 0.01% to about 10%, preferably from about 0.5% to about 5.0% by weight of the composition.
- compositions of this invention can be added to the compositions of this invention in order to increase their attractiveness, versatility, and shelf-life.
- Perfumes and water soluble, pharmaceutically acceptable dyes or food colors can be added to enhance the attractiveness of these compositions.
- Antifungal and antimicrobial agents are useful in preventing mold or bacterial contamination and in increasing the shelf-life of the compositions.
- Conventional antibacterial agents can be included in the present compositions at levels of from about 0.1% to about 4%, preferably from about 0.2% to about 1%.
- Typical antibacterial agents which are suitable for use herein are 3,4-di- and 3,4',5-tribromosalicylanildes; 4,4'-dichloro-3-(trifluoromethyl)carbanilide; 3,4,4'-trichlorocarbanilide; phenoxy ethanol or propanol; chlorhexidene salts; hexamidine salts; Irgasan DP 300 (Triclosan); salicylic acid; parachlorometaxylenol; Octopirox; and mixtures of these materials.
- skin cleansing compositions having a pH range from about 5.0 to about 8.0 are desirable. If necessary, the pH of these compositions can be adjusted downward using citric or lactic acid.
- a pH of about 6.5 is desirable.
- the nature of the foam produced determines the usefulness of the present compositions. In order for a foam to be useful as a skin cleansing agent, it must have a uniform consistency, good spreadability, and good cleansing ability.
- the foamability and wettability characteristics are governed by the surface tension of the skin cleansing composition.
- the surface tension for the compositions of this invention varies from about 20 to 70 dynes/cm.
- a range of from about 23 to about 50 dynes/cm is preferred.
- Liquid compositions having a surface tension in the lower portion of this range possess greater spreading and better wetting characteristics with increased foamability.
- Foamable compositions having higher surface tensions generally provide more stable foams but are also more difficult to cause to foam and require more force to extrude the foam.
- the foam-producing skin cleansing compositions of this invention are particularly advantageous in that they leave a minimum amount of surfactant residue on the surface of the skin. This has been achieved in part by utilizing a low percentage of total surfactants in the skin cleansing compositions itself, and by preparing foams with unusually low density.
- the present compositions provide foam densities provide good cleansing ability and more Importantly, leave a negligible amount of surfactant residue on the surface of the skin upon rinsing or flattening, thereby preserving skin elasticity, and reducing transepidermal moisture loss.
- the cleansing ability of these aerated foams is a direct function of the cleansing ability of the surfactant solution itself which produces the foam.
- the molten phosphate is slowly added to the N,N,N',N'-tetrakis(2- hydroxypropyl)-ethylenediamine.
- the phosphate is added until a pH of 5.0 to 9.0 is reached (preferably 7.0).
- the resulting N,N,N',N'- tetrakis(2-hydroxypropyl)-ethylenediamine monolaurylphosphate is then cooled to form a clear, yellow solid.
- This solid can be used as a solid bar or as a material to produce liquid cream or gel product.
- a facial cleansing composition for topical administration is prepared by combining the following ingredients:
- a facial cleansing cream composition for topical administration is prepared by combining the following ingredients:
- a facial cleansing composition for topical administration is prepared by combining the following ingredients:
- a facial shaving foam composition for topical administration is prepared by combining the following ingredients:
- a facial cleansing composition for topical administration is prepared by combining the following ingredients:
Abstract
L'invention concerne de nouveaux agents tensio-actifs ayant un faible pouvoir d'initiation de la peau et des compositions d'agents tensio-actifs qui possèdent un fort pouvoir moussant et qui renferment, comme composant actif, un sel phosphate monoalkyle diamine.The invention relates to new surfactants with low skin-initiating power and compositions of surfactants which have high foaming power and which contain a phosphate monoalkyl diamine salt as the active ingredient.
Description
Claims
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US50015190A | 1990-03-27 | 1990-03-27 | |
US500151 | 1990-03-27 | ||
US64552091A | 1991-01-24 | 1991-01-24 | |
US645520 | 1991-01-24 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0521980A1 true EP0521980A1 (en) | 1993-01-13 |
EP0521980A4 EP0521980A4 (en) | 1993-08-25 |
Family
ID=27053427
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19910906853 Ceased EP0521980A4 (en) | 1990-03-27 | 1991-03-11 | Novel surfactants and surfactant compositions |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP0521980A4 (en) |
JP (1) | JPH05506018A (en) |
CN (1) | CN1029912C (en) |
AU (1) | AU7581791A (en) |
CA (1) | CA2078442C (en) |
IE (1) | IE911002A1 (en) |
NZ (1) | NZ237587A (en) |
PT (1) | PT97096B (en) |
WO (1) | WO1991014693A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102504615A (en) * | 2011-11-17 | 2012-06-20 | 中国科学院宁波材料技术与工程研究所 | Antibacterial agent preparation method for antibacterial plastic product |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6221822B1 (en) | 1995-10-30 | 2001-04-24 | Tomah Products, Inc. | Detergent compositions having polyalkoxylated amine foam stabilizers |
US5719118A (en) * | 1995-10-30 | 1998-02-17 | Tomah Products, Inc. | Detergent compositions having polyalkoxylated amine foam stabilizers and method for cleaning including stabilized detergent foam |
DE19756373A1 (en) * | 1997-12-18 | 1999-06-24 | Clariant Gmbh | alkyl phosphates |
JP5959932B2 (en) * | 2012-05-18 | 2016-08-02 | 株式会社ダイゾー | Foamable aerosol composition |
US20210069336A1 (en) * | 2017-07-31 | 2021-03-11 | Ohio State Innovation Foundation | Biomimetic nanomaterials and uses thereof |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4290904A (en) * | 1980-12-01 | 1981-09-22 | Neutrogena Corporation | Transparent soap |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2758093A (en) * | 1948-06-22 | 1956-08-07 | Textilana Corp | Laundering compositions containing ortho-phosphoric acid esters |
US3442727A (en) * | 1967-08-03 | 1969-05-06 | Atlas Chem Ind | Emulsified nitric acid blasting composition and method of preparing same |
US3954648A (en) * | 1969-12-22 | 1976-05-04 | Pennwalt Corporation | Coatings removal composition containing an alkali metal hydroxide, an oxygenated organic solvent, and an amine |
JPS6035959B2 (en) * | 1977-06-30 | 1985-08-17 | 日本油脂株式会社 | Dispersed fuel manufacturing method |
US4686058A (en) * | 1981-04-13 | 1987-08-11 | Basf Corporation | Thickened-water based hydraulic fluids |
JPS5874798A (en) * | 1981-10-28 | 1983-05-06 | 花王株式会社 | Shampoo composition |
-
1991
- 1991-03-11 JP JP91507206A patent/JPH05506018A/en active Pending
- 1991-03-11 AU AU75817/91A patent/AU7581791A/en not_active Abandoned
- 1991-03-11 EP EP19910906853 patent/EP0521980A4/en not_active Ceased
- 1991-03-11 WO PCT/US1991/001622 patent/WO1991014693A1/en not_active Application Discontinuation
- 1991-03-11 CA CA 2078442 patent/CA2078442C/en not_active Expired - Fee Related
- 1991-03-21 PT PT9709691A patent/PT97096B/en not_active IP Right Cessation
- 1991-03-26 NZ NZ23758791A patent/NZ237587A/en unknown
- 1991-03-26 IE IE100291A patent/IE911002A1/en unknown
- 1991-03-27 CN CN 91102024 patent/CN1029912C/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4290904A (en) * | 1980-12-01 | 1981-09-22 | Neutrogena Corporation | Transparent soap |
Non-Patent Citations (1)
Title |
---|
See also references of WO9114693A1 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102504615A (en) * | 2011-11-17 | 2012-06-20 | 中国科学院宁波材料技术与工程研究所 | Antibacterial agent preparation method for antibacterial plastic product |
CN102504615B (en) * | 2011-11-17 | 2013-08-07 | 中国科学院宁波材料技术与工程研究所 | Antibacterial agent preparation method for antibacterial plastic product |
Also Published As
Publication number | Publication date |
---|---|
CN1029912C (en) | 1995-10-04 |
CN1055385A (en) | 1991-10-16 |
CA2078442C (en) | 1995-12-05 |
EP0521980A4 (en) | 1993-08-25 |
IE911002A1 (en) | 1991-10-09 |
JPH05506018A (en) | 1993-09-02 |
NZ237587A (en) | 1994-02-25 |
WO1991014693A1 (en) | 1991-10-03 |
PT97096A (en) | 1991-12-31 |
PT97096B (en) | 1998-08-31 |
CA2078442A1 (en) | 1991-09-28 |
AU7581791A (en) | 1991-10-21 |
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