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Publication numberUS3785985 A
Publication typeGrant
Publication dateJan 15, 1974
Filing dateApr 21, 1971
Priority dateApr 21, 1971
Also published asCA984299A, CA984299A1, DE2217738A1
Publication numberUS 3785985 A, US 3785985A, US-A-3785985, US3785985 A, US3785985A
InventorsP Grand
Original AssigneeColgate Palmolive Co
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Cosmetic and textile-treating compositions
US 3785985 A
Abstract  available in
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Claims  available in
Description  (OCR text may contain errors)

United States Patent M 3,785,985 COSNETIC AND TEXTILE-TREATING COMPOSITIONS Paul Sheldon Grand, South Bound Brook, N.J., assignor to Colgate-Palmolive Company, New York, NY. No Drawing. Filed Apr. 21, 1971, Ser. No. 136,204 Int. Cl. Clld 3/28, 3/48 US. Cl. 252-106 2 Claims ABSTRACT OF THE DISCLOSURE A method for solubilizing heavy metal salts of l-hydroxy-2(1H) pyridinethione which comprises the step of forming a solution containing the pyridinethione salt, an aliphatic polyamine and a solvent. Particularly preferred are compositions containing in addition to the above ingredients a cleaning agent.

@=s [S en The heavy metal salts of pyridinethione are complexes of the heavy metal and pyridinethione.

The heavy metal salts of pyridinethione are described in detail in US. Pat. 2,809,971. As there reported, the heavy metal salts of pyridinethione can be prepared by a method which comprises interacting a soluble salt of pyridinethione (e.g. alkali metal or ammonium salt thereof) with a soluble compound of the desired heavy metal. On combination of these reactants, the metal salt precipitates and is recovered. Heavy metal compounds described as suitable reactants include, among others, copper, iron, manganese, tin, mercury, cobalt, chromium, lead, gold, cadmium, nickel, silver, titanium, arsenic, antimony, bismuth, zinc and zirconium. The term heavy metal as employed herein includes heavy non-metals of metallic character, e.g., arsenic, and these are characterized in the aforementioned patent as semi-metals. Preferred heavy metal salts of pyridinethione are zinc, cadmium and zirconium.

The heavy metal salts of pyridinethione are active bactericides and fungicides and certain of them are particularly adaptable to application to skin, hair and textiles.

Zinc omadine specifically is very elfective as a dandruff controlling agent in shampoos and has found wide acceptance in the cosmetic and pharmaceutical arts for use in soaps, shampoos, hairdressings, tonics, rinses, lotions, ointments, salves and others. Some other uses of the zinc salt are as a biologically active agent for cutting oils and coolant systems, as an agent for protecting cellulosic fibers from loss of tensile strength due to action of fungi, and as a preservative for water based paints.

One disadvantage of the heavy metal salts of pyridinethione, such as the zinc salt, is their insolubility in common solvents. The zinc salt, for example, is substantially insoluble in water (20 p.p.m.), ethanol (310 p.p.m.),

3,785,985 Patented Jan. 15, 1974 ice benzene (3-5 p.p.m.), petroleum oils, and most common organic solvents such as ethylene glycol, diethyl ether and isopropanol. The material is slightly more soluble in chloroform (3400 p.p.m.), dimethyl formamide (8100 p.p.m.), and dimethyl sulfoxide (5.13 percent). Accord ingly, it has been found ditlicult to formulate suitable cosmetic, textile treating and other compositions contain ing these heavy metal salts in dissolved form. The few solvents known for the salts are unacceptable especially for cosmetic and textile treating uses and the salts must always be present in such compositions in dispersed form, necessarily rendering the compositions opaque and causing precipitation problems.

It has been suggested that these heavy metal salts can be solubilized in common organic solvents and/or water by combining these salts with an amine or polyalkyleneimine. These compounds have been found to be ineffective in solubilizing the heavy metal salts of pyridinethione as demonstrated below by Examples 9 to 11.

The present invention overcomes the disadvantages of prior-art compositions and inadequacies of prior-art methods. Broadly, the present invention relates to a method of solubilizing heavy metal salts of l-hydroxy- 2(lH)-pyridinethione in water, detergent containing compositions, common organic solvents r0 mixtures thereof which comprises incorporating aliphatic polyamines of the general formula H NfCH CH NH+ H wherein n represents a number from 1 to about 5, into compositions containing heavy metal salts of 1-hydroxy-2(1H)-pyridinethione. An additional advantage of the present invention is that it increases the deposition of heavy metal salts of pyridinethione on substrates such as gelatin, skin and textiles.

In general the compositions of this invention comprises base materials selected from the group consisting of water, organic detergent, common organic solvents and mixtures thereof; heavy metal salts of 1-hydroXy-2(1H)- pyridinethione and aliphatic polyamines having the gen eral formula described above.

The zinc salt of pyridinethione is soluble in water only to the extent of 6 p.p.m. However, as the pH is increased the solubility of the zinc salt increases being 35 ppm. at a pH of 8. According to the present invention, however, the solubility of the zinc salt in compositions containing the described aliphatic polyamines and having a pH of about 9.0 or above is as high as about 100,000 p.p.m. or more.

Because of the present inventions many clear products containing heavy metal salts of pyridinethione are now achievable. Examples of these are clear liquid antidandruff shampoo, clear soluble antidandruff hair groomers, clear soluble antibacterial skin cleansers, soluble substantive phytotoxic agents, soluble antibacterial agents to treat textiles and disposable products, to mention a few.

The prior art warns that incorporating the zinc salt of pyridinethione into formulations containing sequestering agents such as for example ethylenediamine tetraacetic acid and its salts has a very deleterious effect on the biocidal activity of this salt. Less than one part ethylenediamine tetraacetic acid per part pyridinethione salt will show this effect. However, in contradiction to the prior art warning, the aliphatic polyamines of the present invention, which are an important class of chelating compounds used as sequestering agents, do not decrease the biocidal activity and even a two-fold excess of a polyamine such as cliethylene triamine does not reduce the antimicrobial activity of zinc pyridinethione.

Polyamines employable in the invention for solubilizing heavy metal pyridinethione salts are ethylene diamine 3 (EDA) diethylene triamine (DETA) triethylene tetramine (TETA), tetraethylene pentamine (TEPA), and pentaethylene hexamine ('PEHA).

The aliphatic polyamines will constitute a minor pro portion of the compositions contemplated depending upon the amount of heavy metal salt of pyridinethione present. The ratio of aliphatic polyamine to \pyridinethione heavy metal salt is generally about /z:1 to about :1. Preferaby the ratio is about 1:1 to about 2: 1.

In view of their antimicrobial effectiveness and of their substantivity, solubilized, pyridinethione heavy metal salts are particularly suitable for improving the condition of the hair, skin and textiles such as fabrics. More particularly, the solubilized salts may be incorporated into compatible cosmetic and textile treating vehicles to form cosmetic compositions for application to their hair and skin to improve the condition, including general health, thereof and textile treating compositions for application to textiles in particular fabrics rendering them sanitary.

By suitable selections of compatible cosmetic vehicles, it is contemplated that the present cosmetic compositions may be prepared in the form of daily skin or hair conditioning products such as skin lotions or hair conditioning rinses, daily hair-grooming products, such as hair lotions, hair sprays and dressings, hair tonics, and the like, or they may be prepared in the form of cleansing products, such as hair shampoos.

By suitable selections of compatible, textile treating vehicles, it is contemplated that present textile treating compositions may be prepared in the form of antibacterial compositions for treating fabrics, disposable products such as diapers, and cellulosic fibers to protect them from loss of tensile strength.

The heavy metal salts of pyridinethione will constitute generally a minor proportion, on the order of about percent to 20 percent by weight of the compositions, but the proportion will vary depending on the nature of the product. Generally concentrations of pyridinethione heavy metal salts in the range of /2 percent to percent by weight of the composition are preferred for cosmetic and textile treating products. More preferred are concentrations of /2 percent to 5 percent, and most preferred are concentrations of /2 to 2 percent by weight of the total composition.

The vehicle accounts for the balance of about 99.25 percent to about 70 percent by weight of the cosmetic skin, and hair compositions, and textile treating compositions and its specific composition will vary according to the end use of the composition. The proportions of all vehicle compositions are expressed as percent by weight of the total composition.

The vehicle in liquid, hairor skin-compositions may be water, common organic solvents or mixtures thereof. Suitable common organic solvents are C -C lower monohydric or polyhydric alcohols such as ethanol, propanol, isopropanol, glycerine, dimethylformamide, dimethylacetamide, and dimethylsulfoxide, to mention a feW.

In liquid hair-grooming compositions generally the vehicle will contain from about 0.5 percent to 65 percent and preferably 3 to 50 percent by weight of a nonvolatile hairgrooming agent.

The balance of the vehicle will vary according to the form of the resultant product, and generally will be an aqueous medium, such as water or mixtures of water and a lower monohydric alcohol, such as ethanol or isopropanol. In the aqueous alcoholic mixtures, as little as 5 percent by weight of water may be present with the balance being lower alcohol. Generally water is about 30 percent to 80 percent by weight of the vehicle.

In liquid cleansing compositions, such as shampoos, and textile treating compositions, the vehicle will generally contain about 10 to 50 percent, preferably about to 35 percent by weight of a compatible, water-soluble synthetic organic detergent and a balance of water and/or other components.

In the case of liquid cleansing compositions for the hair and skin, such as shampoo and textile treating compositions, suitable water-soluble synthetic, organic detergents may be selected from the group consisting of anionic, nonionic, amphoteric, zwitterionic, polar nonionic, and cationic detergents, and mixtures of two or more of the foregoing detengents.

The compatible anionic surface active agents include those surface active or detergent compounds which contain an organic hydrophobic group containing generally 8 to 26 carbon atoms and preferably 10 to 18 carbon atoms in their molecular structure, and at least one water-solubilizing group selected from the group of sulfonate, sulfate, carboxylate, phosphonate and phosphate so as to form a water-soluble detergent.

Examples of suitable anionic detergents which fall within the scope of the anionic detergent class include the water-soluble salts, e.g., the sodium, ammonium, and alkylolammonium salts, of higher fatty acids or resin salts containing about 8 to 20 carbon atoms, preferably 10 to 18 carbon atoms. Suitable fatty acids can be obtained from oils and waxes of animal or vegetable origin, e.g., tallow, grease, coconut oil, tall oil and mixtures thereof. Particularly useful are the sodium and potassium salts of the fatty acid mixtures derived from coconut oil and tallow, e.g., sodium coconut soap and potassium tallow soap.

The anionic class of detergents also includes the watersoluble sulfated and sulfonated synthetic detergents having an alkyl radical of 8 to 26, and preferably about 12 to 22 carbon atoms, in their molecular structure. (The term alkyl includes the alkyl portion of the higher acyl radicals.)

Examples of the sulfonated anionic detergents are the higher alkyl mononuclear aromatic sulfonates such as the higher alkyl benzene sulfonates containing from 10 to 16 carbon atoms in the higher alkyl group in a straight or branched chain, e.g., the sodium, potassium and ammonium salts of higher alkyl benzene sulfonates, higher alkyl toluene sulfonates, higher alkyl phenol sulfonates, and higher naphthalene sulfonates. A preferred sulfonate is linear alkyl benzene sulfonate having a high content of 3-(or higher) phenyl isomers and a correspondingly low content (well below 50 percent) of 2-(or lower) phenyl isomers, i.e., wherein the benzene ring is preferably attached in large part at the 3 or higher (e.g., 4, 5, 6 or 7) position of the alkyl group and the content of isomers in which the benzene ring is attached at the 2 or 1 position is correspondingly low. Particularly preferred materials are set forth in US. Pat. 3,320,174.

Other suitable anionic detergents are the olefin sulfonates, including long-chain alkene sulfonates, long-chain hydroxyalkane sulfonates or mixtures of alkene-sulfonates and hydroxylalkane-sulfonates. These olefin sulfonate detergents may be prepared in a known manner by the reaction of with long-chain olefins containing 8 to 25, preferably 12-21, carbon atoms and having the formula RCH=CHR where R is a higher alkyl group of 6 to 23 carbons and R is an alkyl group of 1 to 17 carbons or hydrogen to form a mixture of sultones and alkenesulfonic acids which is then treated to convert the sultones to sulfonates. Other examples of sulfate or sulfonate detergents are paraflin sulfonates containing about 1020, preferably about 15-20 carbon atoms, e.g., the primary parafiin sulfonates made by reacting long-chain alpha olefins and bisulfites and paraffin sulfonates having the sulfonate groups distributed along the parafiin chain as shown in U.S. Pats. 2,503,280; 2,507,088; 3,260,741; 3,372,188 and German Pat. 735,096; sodium and potassium sulfates of higher alcohols containing 8 to 18 carbon atoms such as sodium lauryl sulfate and sodium tallow alcohol sulfate; sodium and potassium salts of a-sulfofatty acid esters containing about 10 to 20 carbon atoms in the acyl group, e.g., methyl a-sulfomyristate and methyl OL-SlllfO-t3llOWfltC, ammonium sulfates of monoor diglycerides of higher (C -C fatty acids, e.g., stearic monoglyceride monosulfate; sodium and alkylolammonium salts of alkyl polyethenoxy ether sul fates produced by condensing 1 to 5 moles of ethylene oxide with one mole of higher (C -C alcohol; sodium hi gher alkyl (C -C glyceryl ether sulfonates; and sodium or potassium alkyl phenol polyethenoxy ether sulfates with about 1 to 6 oxyethylene groups per molecule and in which the alkyl radicals contain about 8 to about 12 carbon atoms.

The suitable anionic detergents include also the (I -C acyl sarcosinates (e.g. sodium lauroyl sarcosinate), sodium and potassium salts of the reaction product of higher fatty acids containing 8 to 18 carbon atoms in the molecule esterified with isethionic acid, and sodium and potassium salts of the C -C acyl N-methyl taurides, e.g., sodium cocoyl methyl taurate and potassium stearoyl methyl taurate.

Anionic phosphate surfactants in which the anionic solubilizing group attached to the hydrophobic group is an oxyacid of phosphorous are also useful in the detergent compositions. Suitable phosphate surfactants are the sodium potassium and ammonium alkyl phosphate esters such as (RO) PO M and ROPO M in which R represents an alkyl chain containing from 8 to about 20 carbon atoms or an alkyl phenyl group having 8 to 20 carbon atoms and M represents a soluble cation. The compounds formed by including about one to 40 moles of ethylene oxide in the foregoing esters, e.g. [R-O- (EtO) PO M, are also satisfactory.

The particular anionic detergent salt will be suitably selected depending upon the particular formulation and the proportions therein. Suitable salts include the ammonium, substituted ammonium (mono-, diand triethanolammonium), alkali metal (such as sodium and potassium) and alkaline earth metal (such as calcium and magnesium) salts. Preferred salts are the ammonium, triethanolammonium, sodium and potassium salts of the higher alkyl sulfates and the C C acyl sarcosinates.

The nonionic synthetic organic detergents are generally the condensation product of an organic aliphatic or alkyl aromatic hydrophobic compound and hydrophilic ethylene oxide groups. Practically any hydrophobic compound having a carboxy, hydroxy, amido, or amino group with a free hydrogen attached to the nitrogen can be condensed with ethylene oxide or with the polyhydration product thereof, polyethylene glycol, to form a nonionic detergent. Further, the length of the polyethenoxy chain can be adjusted to achieve the desired balance between the hydrophobic and hydrophilic elements.

The nonionic detergents include the polyethylene oxide condensate of one mole of alkyl phenol containing from about 6 to 12 carbon atoms in a straightor branchedchain configuration with about 5 to 30 moles of ethylene oxide, e.g., nonyl phenol condensed with 9 moles of ethylene oxide, dodecyl phenol condensed with 15 moles of ethylene oxide and dinonyl phenol condensed with 15 moles of ethylene oxide. Condensation products of the corresponding alkyl thiophenols with 5 to 30 moles of ethylene oxide are also suitable.

Still other suitable nonionics are the polyoxyethylene polyoxypropylene adducts of l-butanol. The hydrophobe of these nonionics has a minimum molecular weight of 1000 and consists of an aliphatic monohydric alcohol containing from 1 to 8 carbon atoms to which is attached a heteric chain of oxyethylene and oxypropylene. The weight ratio of oxypropylene to oxyethylene covers the range of 95:5 to 85:15. Attached to this is the hydrophilic polyoxyethyleue chain which is from 44.4 to 54.6 percent of the total molecular Weight of 1400 to 4000.

Also included in the nonionic detergent class are the condensation products of a higher alcohol containing about 8 to 18 carbon atoms in a straight or branchedchain configuration condensed with about 5 to 30 moles of ethylene oxide, e.g., lauryl-myristyl alcohol condensed with about 16 moles of ethylene oxide.

A particularly useful group of nonionics is marketed under the trade name Pluronics. The compounds are formed by condensing ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol. The molecular weight of the hydrophobic portion of the molecule is of the order of 950 to 4000, preferably 1200 to 2500. The addition of polyoxyethylene radicals to the hydrophobic portion tends to increase the solubility of the molecule as a whole. The molecular weight of the block copolymers varies from 1100 to 15,000 and the polyethylene oxide content may comprise 20 to percent by weight.

Other suitable nonionics may be derived by the condensation of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylene diamine. The molecular weight varies from 500 to 4500.

Other nonionic detergents include the ethylene oxide addends of monoesters of hexahydric alcohols and inner ethers thereof with higher fatty acids containing about 10 to 20 carbon atoms, e.g., sorbitan monolaurate, sorbitan mono-oleate, and mannitan monopalmitate.

The amphoteric detergents which can be used in the compositions of this invention are generally water-soluble salts of derivatives of aliphatic amines which contain at least one cationic group, e.g., non-quaternary nitrogen, quaternary ammonium, or quaternary phosphonium group, at least one alkyl group of about 8 to 18 carbon atoms and an anionic water-solubilizing carboxyl, sulfo, sulfato, phosphato or phosphono group in their molecular structure. The alkyl group may be straight chain or branched and the specific cationic atom may be part of a heterocyclic ring.

Examples of suitable ampholytic detergents include the alkyl beta-aminopropionates,

RN(H)C H COOM the alkyl beta-iminodipropionates,

RN(C H,COOM) the alkyl and hydroxy alkyl taurinates,

RN (CH C H SO M and the long-chain imidazole derivatives having the following formulas:

wherein R is an acyclic group of about 7 to 17 carbon atoms, W is selected from the group of ROH, R COOM, and R OR COOM Y is selected from the group consisting of OH, R OSO R is an alkylene or hydroxyalkylene group containing 1 to 4 carbon atoms, R is selected from the group consisting of alkyl, alkyl aryl and fatty acyl glyceride groups having 6 to 18 carbon atoms in the: alkyl or an acyl group; and M is a water-soluble cation, e.g., sodium potassium, ammonium or alkylolammonium.

Formula I detergents are disclosed in vol. II of Surface Active Agents and Detergents and in French Pat. 1,412,921 and Formula II detergents are described in US. Pats. 2,773,068, 2,781,354, and 2,781,357. The acyclic groups may be derived from coconut oil fatty acids (a mixture of fatty acids containing 8 to 18 carbon atoms), lauric fatty acid, and oleic fatty acid and the preferred groups are C C alkyl groups. Preferred detergents are sodium N-lauryl beta-aminopropionate, disodium N-lauryl iminodipropionate, and the disodium salt of Z-lauryl-cyclomidium 1 hydroxyl, l-ethoxy-ethanoic acid, l-ethanoic acid.

Zwitterionic detergents such as the betaines and sulfobetaines having the following formula are also useful:

wherein R is an alkyl group containing about to 18 carbon atoms, R and R are each C C alkyl, R is an alkylene or hydroxyalkylene group containing about 1 to 4 carbon atoms, and X is C or 8:0. The alkyl group can contain one or more intermediate linkages such as amido, either or polyether linkages or non-functional substituents such as hydroxyl or halogen which do not substantially affect the hydrophobic character of the group. When X is C, the detergent is called a betaine; and when X is 8:0, the detergent is called a sulfobetaine or sultaine. Preferred betaine and sulfobetaine detergents are l-(lauryl dimethylammonio) acetate, l-(myristyl dimethylammonio) propane-3-sulfonate, and 1-(myristyldimethylammonio)-2-hydroxy-propane-3-sulfonate.

The polar nonionic detergents are those in which the hydrophilic group contains a semi-polar bond directly between two atoms, for example, N- O; P- O, As O, and S O. There is charge separation between the two direct- 1y bonded atoms, but the detergent molecule bears no net charge and does not dissociate into ions.

The polar nonionic detergents of this invention include open-chain aliphatic amine oxides of the general formula R R R N O. For the purposes of this invention R is an alkyl, alkenyl, or monohydroxyalkyl radical having about 10 to 16 carbon atoms. R and R are each selected from the group consisting of methyl, ethyl, propyl, ethanol, and propanol radicals.

Other operable polar nonionic detergents are the openchain aliphatic phosphine oxides having the general formula. R R R P O wherein R is an alkyl, alkenyl, or monohydroxyalkyl radical ranging in chain length from 10 to 18 carbon atoms, and R and R are each alkyl and monohydroxyalkyl radicals containing from 1 to 3 carbon atoms.

Cationic surface active agents may also be employed. Such agents are those surface active detergent compounds which contain an organic hydrophobic group and a cationic solubilizing group. Typical cationic solubilizing groups are amine and quaternary groups.

Examples of suitable synthetic cationic detergents are normal primary amines RNH wherein R is C C the diamines such as those of the type RNHC H NH wherein R is an alkyl group of about 12 to 22 carbon atoms, such as N-Z-aminoethyl stearyl amine and N-Z-aminoethyl myristyl amine; amide-linked amines such as those of the type R CONHC H NH wherein R is an alkyl group of about 8 to 20 carbon atoms, such as N-2-amino ethylstearyl amide and N-amino ethylmyristyl amide; quaternary ammonium compounds wherein typically one of the groups linked to the nitrogen atom is an alkyl group of about 8 to 22 carbon atoms and three of the groups linked to the nitrogen atom are alkyl groups which contain 1 to 3 carbon atoms, including alkyl groups bearing inert substituents, such as phenyl groups, and there is present an anion such as halogen, acetate, 'methosulfate, etc. The alkyl group may contain intermediate linkages such as amido which do not substantially affect the hydrophobic character of the group, e.g., stearyl amido propyl quaternary ammonium chloride. Typical quaternary ammonium detergents are ethyl dimethyl stearyl ammonium chloride, benzyl-dimethyl-stearyl ammonium chloride, trimethylstearyl ammonium chloride, trimethyl-cetyl ammonium bromide, dimethyl-ethyl-lauryl ammonium chloride, dimethyl-propyl-myristyl ammonium chloride, and the corresponding methosulfates and acetates.

The cosmetic compositions for the hair and skin may also contain as adjuvant materials various substances, such as vitamins, lanolin, bacteriocides, plant extracts, coloring agents, perfumes, thickeners such as cellulose, opacifiers, and sequestering agents in order to enhance the cosmetic or antimicrobial properties of the resultant compositions. Butfers may also be included to provide a suitable pH depending upon the nature of the product prepared.

The hair, skin and textile treating compositions of the invention which contain solubilized heavy metal salts of pyridinethione are characterized by an outstanding ability to inhibit the growth of P. ovale, the yeast believed to be associated with dandruff. The aliphatic polyamine renders the active ingredient substantive (remain on the hair and skin) and therefore the period of time of bacteriostatic effect is extended.

The following examples further illustrate and describe the invention.

Examples 1-6 illustrate water and detergent compositions containing solubilized zinc 1 hydroxy 2(1H)- pyridinethione.

EXAMPLE 1 Biocidal composition To 0.75 g. zinc pyridinethione is added 47.75 g. water. This 48.5 g. slurry is stirred for 1 minute. To this slurry is added 1.5 g. of BETA. Zinc pyridinethione is completely dissolved. It is observed that mixing the aliphatic polyamine and the heavy metal salt before diluting with water results in a clear yellow solution. To obtain a clear colorless solution it is preferred to dilute either the aliphatic polyamine or the heavy metal salt of pyridinethione with grater or solvent prior to the addition of the other ingreient.

Similar results are obtained with other salts of pyridinethione, e.g., cadmium and zirconium salts.

Other suitable formulations productive of desired results are illustrated in Examples 24.

EXAMPLE 2 Percent by weight Desired results are also obtained with similar formulations containing pentaethylene hexamine (PEHA) and ethylene diamine (EDA).

9 EXAMPLE 5 The following is an example of an anionic shampoo having biocidal activity:

This shampoo is prepared as follows: To 1.5 g. zinc pyridinethione and 15.5 g. water is added 3.0 g. DETA. T this 20.0 g. solution of slurry is added 80 g. of the following anionic base: 24.20 g. TEALS (41.1% A.I. 33.70 g. LDMAO (29.65% A.I.), 5.0 g. CMA and 10.50 g. ETOH (95% A.I.) and 6.6 g. H O. This composition is prepared by combining TEALS, LDMAO, CMA and water at room temperature (2025 C.) heating with stirring to about 150 F., cooling to room temperature, adding ETOH and adjusting with water to 80 g. The base is combined and stirred at room temperature with zinc pyridinethione, water and DETA. A crystal clear shampoo results having biocidal activity.

Desired results are also obtained with triethylene tetramine (TETA) as the solubilizing polyamine.

EXAMPLE 6 The following is an example of an amphoteric shampoo having biocidal activity:

Percent by weight C C alkyl amidopropyl dimethyl betaine (CADG) 16.0

Triethanolamine lauryl sulfate (TEALS) 4.0 Lauryl dimethylamine oxide (LDMAO) 0.5 Mixed polymer having a molecular weight of about 4000 formed by condensing a 1:1 mixture of ethylene oxide and propylene oxide on butanol (Ucon 50 HB 5100 2.00 Resinous condensate of about 2 moles of epichlorohydrin and one mole of diethylene triamine having a molecular weight of about 80,000 0.50 Polyoxypropylene-polyoxyethylene block copolymer wherein the hydrophobic group has a molecular weight of 1,750 and ethylene oxide is 20% by weight (Pluronic L62) 5.00 Ethanol (ETOH) 2.00 Zinc pyridinethione 1.50 Diethylenetriamine (DETA) 3.00 Water 65.50

This shampoo is prepared in the same manner described in Example 2. A crystal clear shampoo results.

EXAMPLE 7 The results of an experiment to show that the antimicrobial activity of zinc pyridinethione is maintained when the salt is solubilized by the aliphatic polyamines of this invention are disclosed in Table I.

The microbial effectiveness of compositions of the invention containing solubilized heavy metal salts of pyridinethione was determined using the Test Tube Serial Dilution Method described on pp. 195-200 of the th edition of Diagnostic Bacteriology by Schaub et al. Table I sets forth the minimum inhibitory concentration (MIC) as determined using the aforementioned method against P. ovale of these compositions.

A1. means active ingredients.

10 TABLE I MIC in micrograms per milliliter g/ml.) Test composition: against P. ovale 1% diethylenetriamine in water 500 1000 1% ethylene diamine in water 500-) 1000 1% zinc pyridinethione in water 1.9- 7.8

1% Zinc pyridinethione-14% diethylenetriamine in water 1.9 7.8

EXAMPLE 8 In addition to maintaining the antimicrobial activity of heavy metal salts of pyridinethione solubilized by the polyamines, enhanced deposition of zinc pyridinethione on substrates has been observed and is shown in Table II. Deposition was determined by stirring a half-inch diameter circular gelatin disk Weighing about 40 milligrams in 10 grams of 1% by weight of radio-active (zinc 65 tagged) pyridinethione salt, rinsing the disk five times in 10 milliliters of water and measuring the radio-active emission with the aid of a radiation detector.

TABLE 11 Absolute degree of dep- Composition: osition g/disc) Water+1.5% zinc 65 pyridinethione 40.9 Water+1.5% zinc 65 pyridinethione+3% ethylene diamine 181 Water+1.5% Zinc 65 pyridinethione-{ 3% diethylenetriamine 178 Water+1.5% zinc 65 pyridinethione+3% tetraethylenepentamine 181 Shampoo of Example 5 without diethylenetriamine but the Zinc is Zinc 65 8.7 Shampoo of Example 5 where zinc is zinc 65 45.9 Shampoo of Example 5 Where zinc is zine 65 and diethylenetriamine is replaced by ethylene diamine 23 Shampoo of Example 6 where zinc is zinc 65 and diethylenetriamine is replaced by tetraethylenepentamine 43.6

From Table II it is demonstrated that the addition of aliphatic polyamines to water and shampoos containing zinc pyridinethione results in depositions of zinc pyridinethione which are 3 to 21 times amount obtained when aliphatic polyamines. Similar increases in depositions are obtainable with amphoteric shampoos such as described in Example 6.

The experiments in Examples 9 to 11 compare the solubilizing agents suggested 'by the prior art to those of the present invention. These results show that the prior art suggested solnbilizing agents such as polyethyleneimine and diglycol amine are ineffective.

EXAMPLE 9 To 0.75 g. zinc pyridinethione is added 47.75 g. H O. This 48.5 g. slurry is stirred for 1 minute. In two separate experiments, to this slurry is added 1.5 g. of diethylenetriamine (DETA) and diglycolamine (DGA). Also, to 0.75 g. zinc pyridinethione is added 44.75 g. H O. The 45.50 g. slurry is stirred for 1 minute. To this slurry is added 4.5 g. of polyethyleneimine (PEI-1000 (33% A.I.). So, in each of the three experiments there is 1.5% zinc pyridinethione and 3.0% solnbilizer and balance is made up to with water (95.5%). The visual observations of these solutions are recorded in Table III.

PEI-1000 is a polymer of ethylenelmine with average molecular weight:100,000 prepared by polymerization of ethyleneimine and containing a primary-, secondary, tertiaryamine ratio of 1 :2 :1.

TABLE III Visual observations, preparation with- Experimental conditions DE'IA D GA PEI-1000 Stirring at room temperature for 3 Complete solubility of zinc pyridine- Less than solubility of zinc pyri- Approximately solubility of zinc minutes. thione. dinethione. pyridinethione. Hot plate heating until 100 F Maintenance of solubility N o greater solubility. Zine pyridiue- No greater solubility but zinc pyrithione quickly settles. dinethione in uniform suspension. Infinite dilution with R 0 of clear Solubility upon infinite dilution solution. witl water. No cloudiness develope pH of solution unadjusted- 11.5. 11.2. Y 9.3. I Adjusted pH downward with HCL- Start clouding up solution at approx- Excessively less solubilization than Excessively less solublhzatlon than imately pH 9.2. Approximately above observed. above observed.

50% precipitation at pH 8.8.

The degree of solubilization of zinc pyridinethione by The visual observations of these shampoo systems are diethylenetriamine, diglycolamine and polyethyleneimine 15 recorded in Table V.

TABLE V Visual observations Experimental conditions DE'IA D GA PEI-1000 pH, unadj 9.75. 9- 8.6. Visual, unadjusted Crystal clear shampoo Cloudy shampoo, less than 10% zinc Large quantity of gummy-like precipipyridinethione is soluble. tate.

pH adjustment Decrease pH with H01 1 pH 9.3=Clear soluble system; pH 9.2=Slightly cloudy; pH 9.0=Cloudy with slight degree of precipitation; pH 8.5=Cloudy yellow solution with precipitate.

into both an anionic (Table IV) and amphoteric (Table EXAMPLE 11 VI) shampoo base was studled' The following amphoteric shampoo systems are pre- EXAMPLE 10 pared:

The following anionic shampoo systems are prepared: TABLE VI TABLE IV Percent solids of- Percent solids ofp t r I II III I 11 n Cocoamidepropyldimethyl betaine 16.0 16.0 16.0 Triethanolamine laurylsulfato--.- 4.0 4.0 4.0 Triethanolamlne lauryl sulfate (TEALS) 10.0 10.0 10.0 a y thylamine oxide 0.5 0.5 0.5 Lauryl dimethylamine oxide (LDMAO) 10.0 10. 0 10. 0 MlXed polymer havlng a mo ecu ar w 1g of Cocomonoethanol amide (CMA) 5. 0 5. 0 5.0 about 4000 formed by co dens g a 1:1 mix- Ethanol (ETOH) 10.0 10.0 10.0 ture of ethylene oxide and propylene oxide Zinc pyridinethione 1.5 1.5 1.5 n butanol (Ucon 50 HB 100) 2.0 2.0 2.0 Diethylenetriamine (DETA)- 3.0 Resmous condensate of about 2 moles of ep Diglycolamine (DG 3.0 h rq y rln and one mole of diethylene Polyethyleneimine (PEI-1000).. 3. 0 ne having a molecular weight of about H2O 00.5 60.5 60.5 80,000 0.5 0.5 0.5

Polyoxypropylenepolyoxyethylene block co- Total 100.0 100. 0 100.0 po ymer wherein the hydrophobic group has a molecular weight 0! 1,750 and ethylene oxide is 20% by weight (Pluronic L62) 5. 0 5. 0 5. 0 The shampoos are prepared as follows: To 1.5 g. zinc g h 2;.2 g pyridinethione and 15.5 g. H O (as in preparations I and Dieflffienemmim II) or 9.5 g. H O (as in preparation III) is added 3.0 g. Diglycnlemipe 3.0 Pol eth lennm e DETA or 3.0 g. DGA or 9.0 g. (33% Al.) PEI-IOOO- Wa er"? l 65.5 65.5

To this 20.0 g. solution of slurry is added 80 g. of the following shampoo base: 24.20 g. TEALS (41.1% AI). These shampoos are prepared as described in Example 8. 33.70 g. LDMAO (29.65% A.I.), 5.0 g. CMA and 10.50 The visual observations of these shampoo systems are g. ETOH (95% Al) and 6.6 g. H O. The shampoo base recorded in Table VII.

TABLE VII Visual observations Experimental conditions DETA D GA PEI-1000 pH, unadjusted 10.1 9.6. 9.1. Visual, unadjusted Crystal clear solution Yellow translucent liquid with heavy Slightly cloudy solution with heavy white precipitate. white precipitate (smoky color solution). pH adjustment with HCl. Shampoo remains clear down to ap- Yellow translucent liquid with heavy Grey translucent liquid with heavy proximately pH 9.3 (smoky color), white precipitate remains (pH 8.5). white precipitate (pH 8.5). slight degree of white precipitation, between pH 9.0 to 8.5 (with cloudy grey colored solution). pH adjusted with NaOH Clear soluble solution remains A significant portion of zinc pyridine- A significant portion of zinc pyridinethroughout. thlone doesnt begin to solubilize thione doesn't begin to solubilize anti; above pH 12.0 (yellow soluuntil above pH 12.0 (yellow solution).

is prepared by combining TEALS, LDMAO, CMA and From the results of the experiments disclosed in Tables H O at room temperature, heating with stirring to 150 V and VII, it is evident that the aliphatic polyamines such F., cooling to room temperature, adding ETOH and adas diethylene triamine are effective solubilizing agents justing with H O to 80.0 g. The base was combined and for heavy metal salts of pyridinethione and they are far stirred at room temperature with zinc pyridinethione and superior to the prior art suggestions such as diglycolamine H 0 and solubilizer (DETA, DGA or PEI-1000) combiand pyridinethione. Only the aliphatic polyamines are efnation. fective solubilizers in the pH range suitable for toilet and household products such as shampoos and textile treating compositions.

The following examples illustrate other compositions which make use of the present invention. These examples are merely illustrative and do not limit the scope of use of the invention.

EXAMPLE 12 Hair groomer Percent by weight Ethanol 70 Isopropyl myristate 10 Zinc pyridinethione 2 Diethylene triamine 3.5 Perfume 0.4 Water 14.1

100.0 EXAMPLE 13 Phytotoxic agent Percent by weight Zinc pyridinethione 10.0 Diethylene triamine 20.0 Water 70.0

EXAMPLE 14 Textile treating composition Percent by weight Sodium tridecylbenzene sulfonate 10 Sodium lauryl polyethoxamer sulfate (average of ethylene oxide groups) 3 This composition is bactericidal for a variety of bacteria such as Staph. aureus, Staph. albus, E. coli, to mention a few.

The pH of any of the above solutions may be adjusted by mineral and organic acids such as hydrochloric, sulfuric, citric, oxalic, tartaric, maleic and malic and alkalies such as sodium hydroxide, potassium hydroxide and ammonium hydroxide.

Although the present invention has been described with reference to particular embodiments and examples, in particular the use of the preferred. solubilizer (diethylene triamine), preferred heavy metal salt of pyridinethione (zinc pyridinethione) and preferred solvent (water) in most of the examples, it will be apparent to those skilled in the art that similar results may be obtained with the other ingredients disclosed and their equivalents.

What is claimed is:

1. A method of solubilizing a heavy metal salt of a 1- hydroxy-2-pyridinethione in an aqueous detergent solution, which consists essentially of the step of forming a solution of water, said pyridinethione salt, water-soluble synthetic organic detergent and an aliphatic polyamine selected from the group consisting of ethylene diamine, diethylene triamine, triethylene tetramine, tetraethylene pentamine and pentaethylene hexamine, said solution having a pH of about 9.0 or above in which said pyridinethione salt is A to 20% by weight, said detergent is 10 to 50% by weight and the weight ratio of said aliphatic polyamine to said pyridinethione salt is from about V2 to 1 to about 5 to l and sufiicient to solubilize said pyridinethione salt.

2. A clear liquid detergent composition consisting essentially of A to 20% by weight of a heavy metal salt of l-hydroxy-Z-pyridinethione, 10 to 50% by weight of a water-soluble, synthetic organic detergent, and an aliphatic polyamine selected from the group consisting of ethylene diamine, diethylene triamine, triethylene tetramine, tetraethylene pentamine and pentaethylene hexamine, the weight ratio of said amine to said pyridinethione salt being from about A: to l to about 5 to 1 and suflicient to solubilize said pyridinethione salt, the balance being water and the pH of the said composition being about 9.0 or above.

References Cited UNITED STATES PATENTS 3,636,213 l/ 1972 Gerstein et a1 424-245 3,108,036 10/1963 Molnar 424347 3,580,853 5/1971 Parran 252- 544 3,003,970 10/1961 Call 252-544 X LEON D. ROSDOL, Primary Examiner P. E. WILLIS, Assistant Examiner U.S. Cl. XR.

Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3940482 *Aug 17, 1973Feb 24, 1976Colgate-Palmolive CompanySolubilization of the zinc salt of 1-hydroxy-2-pyridinethione
US3998785 *Jan 6, 1976Dec 21, 1976International Business Machines CorporationAnti-fungal and/or anti-bacterial hardware for ink printing apparatus
US4033895 *Dec 24, 1975Jul 5, 1977Revlon, Inc.Non-irritating shampoo compositions containing stearyl amine oxide
US4161526 *Jul 20, 1978Jul 17, 1979Sterling Drug Inc.Zinc salt prevention or removal of discoloration in pyrithione, pyrithione salt and dipyrithione compositions
US4184974 *Mar 11, 1977Jan 22, 1980Leuven James W VanLiquid biocidal compositions comprising a mixture of silver ions and sodium pectate
US4235873 *Mar 30, 1979Nov 25, 1980Dermik LaboratoriesAntiperspirant-deodorant compositions
US4267168 *Sep 17, 1979May 12, 1981Aquatain PartnershipMethod of reducing bacteria on human tissue using liquid biocidal compositions comprising a mixture of silver ions and sodium pectate
US4289758 *Aug 18, 1980Sep 15, 1981Aquatain PartnershipLiquid biocidal compositions compriing a mixture of silver ions and sodium pectate
US4450090 *May 16, 1983May 22, 1984Clairol IncorporatedThickened alpha-olefin sulfonate containing formulations
US4470982 *Apr 12, 1982Sep 11, 1984The Procter & Gamble CompanyShampoo compositions
US4632991 *Jan 25, 1985Dec 30, 1986Rutgerswerke AgProcess for production of zinc 2-mercaptopyridine-n-oxide
US4659830 *Jul 15, 1986Apr 21, 1987Rutgerswerke AktiengesellschaftProcess for the production of zinc 2-mercaptopyridine N-oxide
US4835149 *Nov 13, 1986May 30, 1989Basf CorporationSolubilization of salts of pyridine-2-thiol-1-oxide
US5037818 *Jul 26, 1988Aug 6, 1991Chesebrough-Pond's Usa Co., Division Of Conopco, Inc.Washing composition for the hair
US5167872 *Oct 20, 1986Dec 1, 1992The Procter & Gamble CompanyComprising anionic surfactant polymeric nonionic surfactant and betaine surfactant
US5227156 *Apr 14, 1992Jul 13, 1993Amway CorporationUse of zinc compounds to stabilize a thiazolinone preservative in an anti-dandruff shampoo
US5540860 *Feb 28, 1994Jul 30, 1996Olin CorporationProcess for preparing copper pyrithione
US5650095 *Jan 22, 1996Jul 22, 1997Olin CorporationProcess for preparing copper pyrithione
US20140272152 *Aug 10, 2012Sep 18, 2014Kimio SuzukiAgent for imparting anti-bacterial/anti-fungal properties, fiber processing agent, and production method for anti-bacterial/anti-fungal fiber
DE2736019A1 *Aug 10, 1977Mar 2, 1978Kao CorpHaarwaschmittel mit geringer hautreizung
WO1995022905A1 *Feb 23, 1995Aug 31, 1995Olin CorporationProcess for preparing copper pyrithione
WO2000005961A1 *Jul 27, 1999Feb 10, 2000Nicca Chemical Co., Ltd.Antibacterial and mildewproofing agents for fibers, antibacterial and mildewproofing processing method and antibacterial and mildewproofing fiber products
Classifications
U.S. Classification514/188, 510/383, 510/124, 510/131, 510/492, 546/6
International ClassificationC11D3/28, D06M13/248, C07D213/89, A61K8/49, A61Q5/02, A01N43/40, A61Q19/00, D06M16/00, A61K8/41, C11D3/48
Cooperative ClassificationA61Q19/00, A61Q5/02, C11D3/48, D06M13/248, A01N43/40, A61K8/41, A61K8/4933, D06M16/00, A61Q17/005
European ClassificationC11D3/48, A01N43/40, A61K8/49C6, D06M16/00, A61Q19/00, A61Q5/02, A61K8/41, D06M13/248, A61Q17/00F