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US3769398A - Polyethylenimine shampoo compositions - Google Patents

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US3769398A
US3769398A US3769398DA US3769398A US 3769398 A US3769398 A US 3769398A US 3769398D A US3769398D A US 3769398DA US 3769398 A US3769398 A US 3769398A
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shampoo
oxide
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pei
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G Hewitt
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Colgate-Palmolive Co
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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL AND VEGETABLE OILS, FATS, FATTY SUBSTANCES AND WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3723Polyamines, polyalkyleneimines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K8/00Cosmetics or similar toilet preparations
    • A61K8/18Cosmetics or similar toilet preparations characterised by the composition
    • A61K8/30Cosmetics or similar toilet preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toilet preparations characterised by the composition containing organic compounds containing nitrogen
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K8/00Cosmetics or similar toilet preparations
    • A61K8/18Cosmetics or similar toilet preparations characterised by the composition
    • A61K8/30Cosmetics or similar toilet preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toilet preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • A61K8/442Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K8/00Cosmetics or similar toilet preparations
    • A61K8/18Cosmetics or similar toilet preparations characterised by the composition
    • A61K8/72Cosmetics or similar toilet preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toilet preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILET PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILET PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S424/00Drug, bio-affecting and body treating compositions
    • Y10S424/02Resin hair settings
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S424/00Drug, bio-affecting and body treating compositions
    • Y10S424/04Dandruff

Abstract

CLEAR, VISCOUS, HOMOGENEOUS SHAMPOO COMPOSITIONS WHICH HAVE EXCELLENT CONDITIONING CHARACTERISTICS ARE EFFECTIVE AGAINST PITYROSPORUM OVALE CONTAINING AS THE ACTIVE INGREDIENTS A DETERGENT SELECTED FROM THE GROUP CONSISTING OF BETAINES, SULFOBETAINES, AMINE OXIDES, AND MIXTURES THEREOF, A WATER-SOLUBLE POLYMER SELECTED FROM THE GROUP CONSISTING OF POLYETHYLENIMINES, ETHOXYLATED POLYETHYLENIMINES, AND PROPOXYLATED POLYETHYLENIMINES HAVING A MOLECULAR WEIGHT FROM ABOUT 1,800 TO ABOUT 500,000, AND AN AQUEOUS VEHICLE.

Description

United States Patent 3,769,398 POLYETHYLENIMINE SHAMPOO COMPOSITIONS Gordon Trent Hewitt, Upper Montclair, N.J., assignor to Colgate-Palmolive Company, New York, NY. No Drawing. Filed May 25, 1970, Ser. No. 40,385

Int. Cl. A61k 7/06 US. Cl. 424-70 8 Claims ABSTRACT OF THE DISCLOSURE This invention relates to clear, viscous, homogeneous shampoo compositions which have outstanding hair conditioning characteristics and are effective against Pityrosporum ovale. The instant shampoo compositions have all of the basic characteristics of commercially acceptable shampoos-they clean but maintain hair luster, are clear, viscous, and homogeneous, condition hair and leave it easy to manage (no static flyaway or tangles), and form copious, lather even in hard water.

The inventive compositions are also suitable for cleaning and conditioning the human hair which is used to make hairpieces such as Wigs and toupees. It is considered that the hair in such hairpieces should be free of the P. ovale yeast in order to eliminate or minimize the problems associated with migration of such yeast to the scalp of the hairpiece wearer. Since the described compositions efiectively inhibit the growth of P. ovale, they are particularly suitable for cleaning the hair prior to or after its fabrication into hairpieces.

It is, therefore, an object of this invention to provide clear, stable, homogeneous shampoo compositions which have excellent hair conditioning characteristics, and inhibit the growth of P. ovale.

In general the preferred compositions of this invention are comprised of from about to about 25 percent by weight of a betaine, sulfobetaine, or amine oxide detergent, and mixtures thereof, from about 0.1 to about 3.0 percent by weight of a water-soluble polyethylenimine (PEI), and an aqueous medium and minor ingredients to make the balance of the composition. Ad ditionally, an imidazoline or oxazoline foam booster may be added in an amount of from about 1.0 to about 6.0 percent by weight of the total composition.

The pH of the composition ranges from about 5.0 to about 9.0 but is preferably adjusted to the near neutral range of 6.5 to 8.0. A lower pH will help solubilize the imidazoline or oxazoline foam booster and enhance their cationic nature; however, too low a pH means that free fatty acids in the natural hair oils will be more tenacious and not as readily removed by the surfactant. A pH of about 7.5 is most preferred.

Patented Oct. 30, 1973 ice It has been found that PEI in a free and uncomplexed form is an outstandingly good antimicrobial agent having both inhibitory activity against P. ovale (MIC of 3.9 ,ug./ml.) and substantivity to the hair and scalp. PEI, however, is a cationic polyamine and has been found to complex strongly with the usual anionic-acting shampoo surfactants, including amphoterics at their useful alkaline pH values and soaps. When PEI is present in a shampoo along with an anionic-acting surfactant, the PEI loses its antimicrobial characteristics; the complex of PEI with the anionic surfactant seems to destroy this extremely valuable property. However, PEI can be formulated into a superior shampoo composition and still maintain its valuable antimicrobial characteristics provided that the shampoo compositions contain carefully selected groups of detergents which do not complex with PEI and which themselves exhibit some inhibitory activity toward P. ovale. The useful detergents are the zwitterionic detergents such as the betaines and sulfobetaines and the semi-polar amine oxide detergents. In such non-anionic compositions the PEI is uncomplexed and thus free to act as an antimicrobial agent.

Moreover, as was stated previously, all of the ingredients in these shampoos were chosen on the basis of their own distinct inhibitory action toward P. ovale. Myristyl and palmityl betaine both have MICs against P. ovale of about 250 ng./ml., lauryl betaine of about 500 ,ugJmL, l-hydroxyethyl-Z-coco imidazoline of about 250 ,ug./ml., and lauryl dimethyl amine oXide of about 1250 ,ugjml. Thus all of the active ingredients in the shampoo are effective to a greater or lesser degree against P. ovale.

In order to determine the substantivity of PEI on the hair the Rubine Dye Test is used. In this test a 0.5-percent aqueous solution of Direct Fast Rubine WS dye is adjusted to a pH of 3.5 with acetic acid. Then approximately 0.5 gram of white hair (or wool) is immersed or rubbed (to produce a lather) for 3 minutes in a shampoo solution. The shampoo concentration is approximately 10 parts shampoo to parts water at room temperature to simulate hair shampooing. After thorough rinsing with water the damp hair sample is immersed for 5 minutes in the dye solution at F. The hair is then rinsed thoroughly with room temperature water. The presence of a deep red color indicates that the hair or wool has deposited on its some cationic active substance. In the absence of such an absorbed cationic, the hair color is essentially unchanged, that is, there is no takeup of the Rubine dye.

It was found that the deposits from the instant nonanionic shampoo solutions formed a very strong, very difiicult to remove attachment of Rubine dye indicating excellent substantivity of PEI. PEI, per se, does not deposit from shampoo solutions containing anionics, such as lauryl sulfates and fatty alcohol ether sulfates.

The PEI polymers which can be used in the shampoos of this invention can be prepared by polymerizing ethyl- In a standard laboratory test to determine antimicrobial activity PEI offered almost no general antimicrobial properties as it was ineffective against S. aureus (MIC greater than 500 1.g./Inl.), Str. mitts (MIC greater than 500 ag./ml.), E. 001% (MIC greater than 1000 ag/1111.), Ps. aerugmosa (MIC greater than 1000 ,ug./ml.), 0. albt'cans (MIC of 1000 ,ug./ml.), and A. mger (MIC greater than 1000 ng./ml.). Against T. 'ggettagt/"oplhptes PEI was very modestly inhibitory (MIC of 2 Minimum Inhibitory Concentration (MIC) of an individual substance or formulation needed to inhibit the growth of a particular organism.

enimine in the presence of a catalyst such as carbon dioxide, sodium bisulfite, sulfuric acid, hydrogen peroxide, hydrochloric acid, acetic acid, etc. Specific methods of preparation are described in US. Pats. Nos. 2,182,306, Ulrich et al., granted Dec. 5, 1939; 3,033,746, Moyle et al., granted May 8, 1962; 2,208,095, Esselmann et al., granted July 16, 1940; 2,806,839, Crowther, granted Sept. 17, 1957; and 2,553,969, Wilson, granted May 21, 1951.

Similarly, alkoxylated PEIs can be prepared, for example, by reacting one part by weight ethylene oxide or propylene oxide with one part by weight PEI prepared as described above and having a molecular weight greater than about 1,800. Preferably, the weight ratio of PEI to alkylene oxide is at least about 1:1, but ratios as low as about 1:4 are acceptable.

It is believed that the general structure of the PEI polymer is:

wherein x represents a whole number of suflicient magnitude to yield a polymer of molecular weight greater than about 1800. Generally, x may vary from 14 to about 1500, and preferably x is from 45 to 5,000. Branch chains occur along the polymeric backbone and the relative proportions of primary, secondary, and tertiary amino groups present in the polymer will vary, depending onthe manner of preparation. The distribution of amino groups in a typical PEI is approximately as follows:

The polymers suitable for use in this invention have viscosities (in 1 percent by weight aqueous solutions) ranging from about 1.0 to about 3.0 centipoises (absolute viscosity) when measured by an Ostwald viscometer at 100 F. The molecular weight of the PEI polymers includes the entire range of dermatologically-safe materials. The preferred polymers have an average molecular weight within the range of about 1800 to about 200,000 with the most preferred polymer having an average molecular weight of about 100,000. The molecular weight may range as high as 500,000 for ethoxylated and propoxylated polymers.

The useful zwitterionic detergents are betaines and sulfobetaines having the following general formula:

1'1. where R, is an alkyl group having 10 to about 20 carbon atoms, preferably 12 to 16 carbon atoms, R and R are each alkyl groups having 1 to 3 carbon atoms, R is an alkylene or hydroxyalkylene group having from 1 to 4 carbon atoms, and X is an anion selected from the group consisting of S and COO=. The preferred betaines and sulfobetaines have the following formulas:

where R in each formula is an alkyl group having about to about carbon atoms.

Amido betaines and amido sulfobetaines having the following structure may also be used:

where R in both formulas is an alkyl group having about 10 to about 20 carbon atoms.

The preferred compound from the group of zwitterionic detergents is coco 3 dimethyl betaine.

The useful semi-polar amine oxide detergents have the following general formula:

Amine oxide R R R N 0 where R is an alkyl, alkenyl, or monohydroxyalkyl group having 10 to about 20 carbon atoms, and R and R are each selected from the group consisting of methyl, ethyl, propyl, ethanol, and propanol groups.

The preferred amine oxide detergent is myristyl dimethyl amine oxide.

The useful foam boosters are the imidazoline and oxazoline materials having the following general formulas:

Oxazoline where R is an alkyl group having about 9 to about 17 carbon atoms, and R and R are selected from the group consisting of hydrogen and alkyl and hydroxyalkyl groups containing from 1 to 2 carbon atoms.

Imidazoline oH,-om

where R is an alkyl group having about 9 to about 17 carbon atoms, and R is selected from the group consisting of hydroxy methyl, hydroxyethyl, hydroxypropyl and CH CH OCH CH OH.

In the preparation of the imidazoline and oxazoline foam booster, the carboxyl carbon of the fatty acid reactant becomes part of the ring, and thus the resultant alkyl group contains one less carbon than the corresponding fatty acid.

The preferred imidazoline foam booster is l-hydroxyethyl-2-coco imidazoline; the preferred Oxazoline foam booster is 2-coco-4,4 dihydroxymethyl oxazoline.

A Water-soluble, nonionic synthetic detergent may be substituted for the preferred zwitterionic and amine oxide detergents; however, the resultant shampoo compositions are non-preferred due to the lower foaming properties of the nonionic detergents. Suitable nonionic synthetic organic detergents are generally the condensation product of an organic aliphatic or alkyl aromatic hydrophobic compound and hydrophilic ethylene oxide groups or the polyhydration product thereof, i.e., polyethylene glycol.

The term coco as used herein refers to the mixture of alkyl groups found in the alcohols obtained by hydrogenating the mixture of fatty acids obtained upon hydrolysis of coconut oil, that is, Cs8%; Clo-7%; Cue-48%; C1i17%; C1e-15% and Cur-5%.

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 to form a nonionic detergent. Suitable nonionic detergents include the polyethylene oxide condensate of one mole of alkyl phenol containing from about 6 to about 12 carbon atoms in a straight or branched chain configuration with about 5 to 30 moles of ethylene oxide, e.g., nonyl phenol condensed with 9 moles of ethylene oxide; the condensation product of a higher alcohol containing about 8 to 22 carbon atoms in a straight or branched chain configuration with about 5 to 30 moles of ethylene oxide, e.g., lauryl-myristyl alcohol condensed with 16 moles of ethylene oxide; the condensation product of ethylene oxide on a hydrophobic base formed by the condensation of propylene oxide on propylene glycol wherein the molecular weight of the hydrophobe ranges from about 1,500 to 1,800 and the polyethylene oxide content may comprise up to 50% of the total weight of the condensate; and the ethylene oxide addends of monoesters of hexahydric alcohols and inner ethers thereof with higher fatty acids containing about to 20 carbon atoms,

e.g., sorbitan monolaurate, sorbitan mono-oleate, and mannitan monopalmitate. Alternatively, such nonionic detergents may be used in addition to the preferred betaine, sulfobetaine, and amine oxide detergents in concentrations of about 3% to 10% by weight of the shampoo composition.

The aqueous vehicle may contain an organic solvent such as monohydric and dihydric alcohols containing 2 to 3 carbon atoms. The solvent may be present in an amount of from about 5 to 30 percent by weight and preferably from about 10 to 20 percent.

In the most preferred shampoo compositions, the betaine, sulfobetaine, and amine oxide detergents are present in an amount of 10% to about 20% by weight; the PEI is present in an amount of about 1% to 2% by weight; the imidazoline and oxazoline foam booster is present in an amount of about 3% to 5% by weight; and the aqueous medium or vehicle is the balance. When a mixture of detergents is used, the preferred concentration of the individual detergents is reduced because the total amount of detergent present in the most preferred compositions ranges from about 10% to about 20% by weight.

Various conventional shampoo additives may also be present, for example, compatible nonionic thickeners, perfumes, pH adjusters, sequestering agents, opacifiers, compatible antimicrobial compounds, etc. Such additives are present in their conventional amounts ranging from about 0.4 to about 10 percent by weight. More specifically, coconut monoor diethanolamides and strongly ionizing salts such as sodium chloride and sodium sulfate may be used up to about 5 percent of the formula weight. These compounds serve to aid in the compatibilization of the polymer-detergent composition; however, they are not essential.

EXAMPLE I Shampoo compositions were prepared having the following composition:

EXAMPLE I Coco dimethylbetalneh 10. 0 1o. 0 10. o Myristyl dimethyl amine oxide 5. 0 l-hydroxyethyl-2-coco imidazoline 5.0 2-coeo-4,4-dihydroxymethyl oxazoline 6. 0 Polyethylenimine (M.W. 50,000)-.. 1. 0 1. 0 1. 0 HCl (pH adjustment to about 7.5). 1. 0 1. 0 1. 0 Propylene glycol 5. 0 5. 0 Perfume 0. 4 0. 4 0. 4 Deionized water 1 Balance.

These compositions were clear, stable liquids which yielded copious lather, left hair free from tangles and static flayaway, and showed inhibitory action against the growth of P. ovale.

EXAMPLE II Coco dimethyl sulfobetaine 10.0 l-hydroxyethyl-Z-coco imidazoline 5.0 Polyethylenimine (M.W. 1800) 2.0 HCl (to adjust pH to about 7.5) 1.0 Deionized water Balance EXAMPLE III Myristyl dimethyl betaine 15.0 l-hydroxyethyl-Z-coco imidazoline 2.0 Polyethylenimine (M.W. 100,000) 1.0 HCl (to adjust pH to about 7.5 1.0 Ethanol 10.0 Deionized water Balance EXAMPLE IV Palmityl dimethyl amido betaine 15.0 Polyethylenimine (M.W. 50,000) 2.0 HCl (to adjust pH to about 7.5 1.0 NaCl 3.0 Deionized water Balance EXAMPLE V Myristyl dimethyl amine oxide 10.0 Polyethylenimine (M.W. 1800) 3.0 HCl (pH adjustment to about 7.5) 1.0 Perfume 0.4 Deionized water Balance In order to determine the conditioning efiect of PEI on the hair the following test was conducted.

Clean hair samples (washed in a nonionic surfactant and rinsed in distilled water and in ethanol) were dipped in a 2-percent oleic acid-alcohol solution to provide free fatty acid such as is present on the scalp. After drying the various tresses were shampooed with:

(A) Composition A of Example I (B) Composition A with PEI omitted (C) Shampoo containing 19% triethanolarnine lauryl sulfate and 5% lauryl-myristyl diethanolamide in an aqueous medium.

The shampoo solutions were diluted with water to 10 parts shampoo to parts water to simulate dilution in actual shampooing. The shampooed tresses were rinsed well and dried. As a control tress one of the clean tresses was not treated with oleic acid but was washed with Composition A of Example I.

The results of this test revealed that the tress which had oleic acid on it and washed with Composition A of Example I was low in friction during dry combing, was low in static fly when combed, and felt smooth. However, the tress having-no oleic acid present which was shampooed with Composition A of Example I was difficult to comb and gave static fly. Further, Composition A without PEI also was difiicult to comb and gave static fly. These results indicate that the conditioning effects of Composition A of Example I are probably due to the fact that PEI deposits on the hair and also redeposits the natural oils. Composition A also gave superior conditioning results as compared to the conventional anionic/alkanolamide shampoo whose washed tress also gave static fly and was difficult to comb.

Percentage values employed in the specification and claims refer to percent by weight of the total composition unless otherwise stated.

What is claimed is:

1. A clear, homogeneous shampoo composition particularly suitable for conditioning hair and for inhibiting the growth of Pityrosporum ovale which consists essentially of about 5 to 25 percent by weight of a water-soluble detergent selected from the group consisting of betaines and sulfobetaines having the formula wherein R is alkyl of 10 to 20 carbons, R and R are each alkyl of 1 to 3 carbons, R is alkylene or hydroxyalkylene of 1 to 4 carbons, and X is S or CO C-alkyl betaines of the formula wherein R is an alkyl of to carbons, C-alkyl sultaines of the formula wherein R is an alkyl of 10 to 20 carbons, amine oxides of the formula R R R N O wherein R is an alkyl, alkenyl, or monohydroxyalkyl of 10 to 20 carbons, and R and R are each methyl, ethyl, propyl, ethanol, or propanol, and mixtures of the foregoing detergents; 0.1 to 3 percent by weight of a water-soluble polymer selected from the group consisting of polyethylenimine having a molecular weight from about 1,800 to about 200,000 and the reaction product of said polyethylenimine with either ethylene oxide or propylene oxide in a weight ratio of polyethylenimine to alkylene oxide of at least 1:4, said reaction product having a molecular weight of up to 500,000, said polymer exhibiting inhibitory activity against Pityrosporum ovale; and an aqueous vehicle, said composition being free of anionic-acting surfactants.

2. The shampoo composition as set forth in claim 1 wherein said detergent is a mixture of said betaine or sulfobetaine corresponding to the formula and said amine oxide and said mixture is present in an amount of 10 to 20 percent by weight of the composition.

3. The shampoo composition as set forth in claim 1 wherein said detergent is said amine oxide.

4. The shampoo composition as set forth in claim 1 wherein said aqueous vehicle contains from about 10 to 20 percent by weight of the total composition of an organic solvent selected from the group consisting of monohydric and dihydric alcohols containing 2 to 3 carbons.

5. The shampoo composition as set forth in claim 1 wherein said aqueous medium is water.

6. The shampoo composition as set forth in claim 1 wherein said polymer is said polyethylenimine having a molecular weight of about 1,800 to 100,000.

7. The shampoo composition as set forth in claim 1 wherein said detergent is said betaine or sulfobetaine corresponding to the formula 8. The shampoo composition'as set forth in claim 1 which contains in addition from about 1 to 6 percent by weight of the total composition of foam boosting compound selected from the group consisting of an oxazoline having the following structure wherein R is alkyl containing 9 to 17 carbons and R and R are each selected from the group consisting of hydrogen, alkyl containing 1 to 2 carbons, and hydroxyal'kyl containing from 1 to 2 carbons and an imidazoline having the following structure wherein R is alkyl containing 9 to 17 carbons and R is selected from the group consisting of hydroxymethyl, hydroxyethyl, hydroxypropyl, and CH CH OCH CH OH.

References Cited UNITED STATES PATENTS 3,033,746 5/ 1962 Moyle et a1. 424-325 3,098,794 7/ 1963 Dohr et al. 424 X 3,206,512 9/1965 Koebner et a1. 424325 X 3,280,179 10/1966 Ernst 42470 X 3,449,430 6/1969 Dohr et al. 42470 X 3,470,102 9/1969 Heinz 42470 X FOREIGN PATENTS 451,412 5/1968 Switzerland 424316 1,111,708 5/1968 Great Britain 424325 1,078,075 8/ 1967 Great Britain.

OTHER REFERENCES Wells et al., Cosmetics and The Skin, p. 404, Reinhold Publishing Corp. New York, 1964.

American Perfumer and Cosmetics, vol. 84, pp. 37- 39, December 1969.

ALBERT T. MEYERS, Primary Examiner V. C. CLARKE, Assistant Examiner US. Cl. X.R.

252106; 424DIG. 24, 78, 316, 325

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Cited By (60)

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US3890434A (en) * 1971-10-18 1975-06-17 Olin Corp Hair and antiseptic formulations containing adducts of bis-(2-pyridyl-1-oxide) disulfide
US3980091A (en) * 1975-01-06 1976-09-14 Alberto Culver Company Quaternary ammonium compounds in pretreatment of hair before shampooing with an anionic shampoo
US3980769A (en) * 1972-09-05 1976-09-14 L'oreal Shampoo containing a water-soluble cationic polymer
US4027009A (en) * 1973-06-11 1977-05-31 Merck & Co., Inc. Compositions and methods for depressing blood serum cholesterol
US4048301A (en) * 1975-05-28 1977-09-13 L'oreal Shampoo composition containing a detergent and a graft cationic copolymer
JPS52151482U (en) * 1976-05-14 1977-11-16
DE2747355A1 (en) * 1977-10-21 1979-04-26 Edwin Bernard Michaels Antimicrobial compsn. contg. acyl-betaine and amine oxide - giving long term control of body odour
US4172887A (en) * 1973-11-30 1979-10-30 L'oreal Hair conditioning compositions containing crosslinked polyaminopolyamides
US4197865A (en) * 1975-07-04 1980-04-15 L'oreal Treating hair with quaternized polymers
US4201766A (en) * 1977-03-02 1980-05-06 L'oreal Hair conditioning composition and method of using the same
FR2460133A1 (en) * 1979-07-02 1981-01-23 Bristol Myers Co A composition for hair care and its application method
US4277581A (en) * 1973-11-30 1981-07-07 L'oreal Polyamino-polyamide crosslinked with crosslinking agent
USRE30874E (en) * 1975-01-06 1982-03-02 Alberto-Culver Company Quaternary ammonium compounds in pretreatment of hair before shampooing with an anionic shampoo
US4329335A (en) * 1980-11-10 1982-05-11 Colgate-Palmolive Company Amphoteric-nonionic based antimicrobial shampoo
USRE31126E (en) * 1975-01-06 1983-01-18 Alberto-Culver Company Quaternary ammonium compounds in pretreatment of hair before shampooing with an anionic shampoo
US4381919A (en) * 1975-07-04 1983-05-03 Societe Anonyme Dite: L'oreal Hair dye composition containing quaternized polymers
DE3445410A1 (en) * 1983-12-22 1985-07-04 Colgate Palmolive Co Reaction product of positively charged cationic polymer and negatively charged anionic polymeric
US4548744A (en) * 1983-07-22 1985-10-22 Connor Daniel S Ethoxylated amine oxides having clay soil removal/anti-redeposition properties useful in detergent compositions
US4551506A (en) * 1982-12-23 1985-11-05 The Procter & Gamble Company Cationic polymers having clay soil removal/anti-redeposition properties useful in detergent compositions
US4597898A (en) * 1982-12-23 1986-07-01 The Proctor & Gamble Company Detergent compositions containing ethoxylated amines having clay soil removal/anti-redeposition properties
US4659802A (en) * 1982-12-23 1987-04-21 The Procter & Gamble Company Cationic compounds having clay soil removal/anti-redeposition properties useful in detergent compositions
US4661288A (en) * 1982-12-23 1987-04-28 The Procter & Gamble Company Zwitterionic compounds having clay soil removal/anti/redeposition properties useful in detergent compositions
US4664848A (en) * 1982-12-23 1987-05-12 The Procter & Gamble Company Detergent compositions containing cationic compounds having clay soil removal/anti-redeposition properties
US4675178A (en) * 1985-05-02 1987-06-23 Calgon Corporation Use of cationic polymers (polydimethyldialkyl ammonium chloride-acrylamide copolymers and dimethyldialkyl ammonium chloride) to increase deposition and/or retention of active agent (S) of deodorant formulations on surfaces
US4676921A (en) * 1982-12-23 1987-06-30 The Procter & Gamble Company Detergent compositions containing ethoxylated amine polymers having clay soil removal/anti-redeposition properties
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US4772462A (en) * 1986-10-27 1988-09-20 Calgon Corporation Hair products containing dimethyl diallyl ammonium chloride/acrylic acid-type polymers
US4891160A (en) * 1982-12-23 1990-01-02 The Proctor & Gamble Company Detergent compositions containing ethoxylated amines having clay soil removal/anti-redeposition properties
US5009887A (en) * 1985-10-31 1991-04-23 Aikoh Co., Ltd. Deodorant composition in the form of a gel
US5186947A (en) * 1990-10-20 1993-02-16 Dr. Wolman Gmbh Wood preservative based on polymeric nitrogen compounds and metal-fixing acids
US5187194A (en) * 1989-10-20 1993-02-16 Dr. Wolman Gmbh Wood preservatives containing polymeric nitrogen compounds
US5503779A (en) * 1995-03-20 1996-04-02 Colgate Palmolive Company High foaming light duty liquid detergent
US5679877A (en) * 1996-06-14 1997-10-21 Colgate-Palmolive Co. Thickened liquid cleaning composition containing an abrasive
US5707955A (en) * 1996-07-15 1998-01-13 Colgate-Palmolive Co. High foaming nonionic surfactant based liquid detergent
US5714454A (en) * 1996-08-07 1998-02-03 Colgate-Palmolive Co. Light duty liquid cleaning compositions comprising alkyl sulroglycerides
US5741769A (en) * 1994-11-23 1998-04-21 Colgate Palmolive Company Microemulsion light duty liquid cleaning compositions
US5756441A (en) * 1996-08-07 1998-05-26 Colgate Palmolive Company High foaming nonionic surfactant based liquid detergent
WO1998023258A1 (en) * 1996-11-29 1998-06-04 Unilever Plc Antimicrobial personal care compositions
US5834417A (en) * 1996-06-13 1998-11-10 Colgate Palmolive Co. Light duty liquid cleaning compositions
US5904735A (en) * 1997-08-04 1999-05-18 Lever Brothers Company Detergent compositions containing polyethyleneimines for enhanced stain removal
US5955415A (en) * 1997-08-04 1999-09-21 Lever Brothers Company, Division Of Conopco, Inc. Detergent compositions containing polyethyleneimines for enhanced peroxygen bleach stability
US20040002550A1 (en) * 2002-06-28 2004-01-01 Mercurio Anthony Fred Post foaming compositions
US20040204331A1 (en) * 2003-04-14 2004-10-14 Colgate-Palmolive Company Antibacterial light duty liquid cleaning composition
US20050020465A1 (en) * 2003-07-23 2005-01-27 Colgate-Palmolive Company Liquid dish cleaning compositions
US20050282721A1 (en) * 2003-07-23 2005-12-22 Gregory Szewczyk Liquid dish cleaning compositions
US20060122092A1 (en) * 2003-08-28 2006-06-08 Gregory Szewczyk Liquid dish cleaning compositions
US20070098768A1 (en) * 2005-11-01 2007-05-03 Close Kenneth B Two-sided personal-care appliance for health, hygiene, and/or environmental application(s); and method of making said two-sided personal-care appliance
US20070142256A1 (en) * 2005-12-15 2007-06-21 Lang Frederick J Health-and-hygiene appliance comprising a dispersible component and a releasable component disposed adjacent or proximate to said dispersible component; and processes for making said appliance
US20070238631A1 (en) * 2006-04-07 2007-10-11 Colgate-Palmolive Company Liquid cleaning composition having low viscosity
US20080274929A1 (en) * 2007-05-01 2008-11-06 Whitekettle Wilson K Method for removing microbes from surfaces
EP2036536A1 (en) * 2007-09-14 2009-03-18 L'Oréal Hair treatment including the application of a polyamine and a fatty acid
US20090074683A1 (en) * 2007-09-14 2009-03-19 L'oreal Compositions and methods for treating keratinous substrates
US20090291053A1 (en) * 2006-03-06 2009-11-26 Sabelko Jobiah J Low molecular weight ampholytic polymers for personal care applications
US20090312225A1 (en) * 2008-06-17 2009-12-17 Colgate-Palmolive Company Light Duty Liquid Cleaning Compositions and Methods of Manufacture and Use Thereof
US20090312227A1 (en) * 2008-06-17 2009-12-17 Colgate-Palmolive Light duty liquid cleaning compositions and methods of manufacture and use thereof
US7651989B2 (en) 2003-08-29 2010-01-26 Kimberly-Clark Worldwide, Inc. Single phase color change agents
US8067350B2 (en) 2005-12-15 2011-11-29 Kimberly-Clark Worldwide, Inc. Color changing cleansing composition
US8247362B2 (en) 2008-06-17 2012-08-21 Colgate-Palmolive Company Light duty liquid cleaning compositions and methods of manufacture and use thereof
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US9464261B2 (en) 2010-05-14 2016-10-11 The Sun Products Corporation Polymer-containing cleaning compositions and methods of production and use thereof

Cited By (77)

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US3890434A (en) * 1971-10-18 1975-06-17 Olin Corp Hair and antiseptic formulations containing adducts of bis-(2-pyridyl-1-oxide) disulfide
US3980769A (en) * 1972-09-05 1976-09-14 L'oreal Shampoo containing a water-soluble cationic polymer
US4027009A (en) * 1973-06-11 1977-05-31 Merck & Co., Inc. Compositions and methods for depressing blood serum cholesterol
US4277581A (en) * 1973-11-30 1981-07-07 L'oreal Polyamino-polyamide crosslinked with crosslinking agent
US4172887A (en) * 1973-11-30 1979-10-30 L'oreal Hair conditioning compositions containing crosslinked polyaminopolyamides
US3980091A (en) * 1975-01-06 1976-09-14 Alberto Culver Company Quaternary ammonium compounds in pretreatment of hair before shampooing with an anionic shampoo
USRE31126E (en) * 1975-01-06 1983-01-18 Alberto-Culver Company Quaternary ammonium compounds in pretreatment of hair before shampooing with an anionic shampoo
US4061150A (en) * 1975-01-06 1977-12-06 Alberto-Culver Company Quaternary ammonium compounds in pretreatment of hair before shampooing with an anionic shampoo
USRE30874E (en) * 1975-01-06 1982-03-02 Alberto-Culver Company Quaternary ammonium compounds in pretreatment of hair before shampooing with an anionic shampoo
US4048301A (en) * 1975-05-28 1977-09-13 L'oreal Shampoo composition containing a detergent and a graft cationic copolymer
US4197865A (en) * 1975-07-04 1980-04-15 L'oreal Treating hair with quaternized polymers
US4381919A (en) * 1975-07-04 1983-05-03 Societe Anonyme Dite: L'oreal Hair dye composition containing quaternized polymers
JPS52151482U (en) * 1976-05-14 1977-11-16
US4201766A (en) * 1977-03-02 1980-05-06 L'oreal Hair conditioning composition and method of using the same
DE2747355A1 (en) * 1977-10-21 1979-04-26 Edwin Bernard Michaels Antimicrobial compsn. contg. acyl-betaine and amine oxide - giving long term control of body odour
DE3024578A1 (en) * 1979-07-02 1981-06-04 Bristol Myers Co Composition for conditioning hair
FR2460133A1 (en) * 1979-07-02 1981-01-23 Bristol Myers Co A composition for hair care and its application method
US4329335A (en) * 1980-11-10 1982-05-11 Colgate-Palmolive Company Amphoteric-nonionic based antimicrobial shampoo
US4664848A (en) * 1982-12-23 1987-05-12 The Procter & Gamble Company Detergent compositions containing cationic compounds having clay soil removal/anti-redeposition properties
US4676921A (en) * 1982-12-23 1987-06-30 The Procter & Gamble Company Detergent compositions containing ethoxylated amine polymers having clay soil removal/anti-redeposition properties
US4891160A (en) * 1982-12-23 1990-01-02 The Proctor & Gamble Company Detergent compositions containing ethoxylated amines having clay soil removal/anti-redeposition properties
US4597898A (en) * 1982-12-23 1986-07-01 The Proctor & Gamble Company Detergent compositions containing ethoxylated amines having clay soil removal/anti-redeposition properties
US4659802A (en) * 1982-12-23 1987-04-21 The Procter & Gamble Company Cationic compounds having clay soil removal/anti-redeposition properties useful in detergent compositions
US4661288A (en) * 1982-12-23 1987-04-28 The Procter & Gamble Company Zwitterionic compounds having clay soil removal/anti/redeposition properties useful in detergent compositions
US4551506A (en) * 1982-12-23 1985-11-05 The Procter & Gamble Company Cationic polymers having clay soil removal/anti-redeposition properties useful in detergent compositions
US4548744A (en) * 1983-07-22 1985-10-22 Connor Daniel S Ethoxylated amine oxides having clay soil removal/anti-redeposition properties useful in detergent compositions
DE3445410A1 (en) * 1983-12-22 1985-07-04 Colgate Palmolive Co Reaction product of positively charged cationic polymer and negatively charged anionic polymeric
US4675178A (en) * 1985-05-02 1987-06-23 Calgon Corporation Use of cationic polymers (polydimethyldialkyl ammonium chloride-acrylamide copolymers and dimethyldialkyl ammonium chloride) to increase deposition and/or retention of active agent (S) of deodorant formulations on surfaces
US5009887A (en) * 1985-10-31 1991-04-23 Aikoh Co., Ltd. Deodorant composition in the form of a gel
EP0266111B1 (en) * 1986-10-27 1993-01-27 Calgon Corporation Personal skin care products containing dimethyl diallyl ammonium chloride/acrylic acid-type polymers
US4772462A (en) * 1986-10-27 1988-09-20 Calgon Corporation Hair products containing dimethyl diallyl ammonium chloride/acrylic acid-type polymers
EP0269243B1 (en) * 1986-10-27 1993-02-03 Calgon Corporation Hair products containing dimethyl diallyl ammonium chloride/acrylic acid-type polymer
US4764365A (en) * 1986-10-27 1988-08-16 Calgon Corporation Personal skin care products containing dimethyl diallyl ammonium chloride/acrylic acid-type polymers
US5187194A (en) * 1989-10-20 1993-02-16 Dr. Wolman Gmbh Wood preservatives containing polymeric nitrogen compounds
US5186947A (en) * 1990-10-20 1993-02-16 Dr. Wolman Gmbh Wood preservative based on polymeric nitrogen compounds and metal-fixing acids
US5741769A (en) * 1994-11-23 1998-04-21 Colgate Palmolive Company Microemulsion light duty liquid cleaning compositions
US5503779A (en) * 1995-03-20 1996-04-02 Colgate Palmolive Company High foaming light duty liquid detergent
US5834417A (en) * 1996-06-13 1998-11-10 Colgate Palmolive Co. Light duty liquid cleaning compositions
US5679877A (en) * 1996-06-14 1997-10-21 Colgate-Palmolive Co. Thickened liquid cleaning composition containing an abrasive
US5707955A (en) * 1996-07-15 1998-01-13 Colgate-Palmolive Co. High foaming nonionic surfactant based liquid detergent
US5756441A (en) * 1996-08-07 1998-05-26 Colgate Palmolive Company High foaming nonionic surfactant based liquid detergent
US5714454A (en) * 1996-08-07 1998-02-03 Colgate-Palmolive Co. Light duty liquid cleaning compositions comprising alkyl sulroglycerides
WO1998023258A1 (en) * 1996-11-29 1998-06-04 Unilever Plc Antimicrobial personal care compositions
US5955415A (en) * 1997-08-04 1999-09-21 Lever Brothers Company, Division Of Conopco, Inc. Detergent compositions containing polyethyleneimines for enhanced peroxygen bleach stability
US5904735A (en) * 1997-08-04 1999-05-18 Lever Brothers Company Detergent compositions containing polyethyleneimines for enhanced stain removal
US20040002550A1 (en) * 2002-06-28 2004-01-01 Mercurio Anthony Fred Post foaming compositions
US20040116544A1 (en) * 2002-06-28 2004-06-17 Mercurio Anthony F. Post foaming compositions
US20060264349A1 (en) * 2003-04-14 2006-11-23 Thomas Connors Antibacterial light duty liquid cleaning composition
US20040204331A1 (en) * 2003-04-14 2004-10-14 Colgate-Palmolive Company Antibacterial light duty liquid cleaning composition
US7087567B2 (en) 2003-04-14 2006-08-08 Colgate-Palmolive Company Antibacterial light duty liquid cleaning composition
US20050282721A1 (en) * 2003-07-23 2005-12-22 Gregory Szewczyk Liquid dish cleaning compositions
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US7115550B2 (en) 2003-08-28 2006-10-03 Colgate-Palmolive Company Liquid dish cleaning compositions
US20060122092A1 (en) * 2003-08-28 2006-06-08 Gregory Szewczyk Liquid dish cleaning compositions
US7651989B2 (en) 2003-08-29 2010-01-26 Kimberly-Clark Worldwide, Inc. Single phase color change agents
US20070098768A1 (en) * 2005-11-01 2007-05-03 Close Kenneth B Two-sided personal-care appliance for health, hygiene, and/or environmental application(s); and method of making said two-sided personal-care appliance
US7612031B2 (en) 2005-12-15 2009-11-03 Kimberly-Clark Worldwide, Inc. Health-and-hygiene appliance comprising a dispersible component and a releasable component disposed adjacent or proximate to said dispersible component; and processes for making said appliance
US20070142256A1 (en) * 2005-12-15 2007-06-21 Lang Frederick J Health-and-hygiene appliance comprising a dispersible component and a releasable component disposed adjacent or proximate to said dispersible component; and processes for making said appliance
US8067350B2 (en) 2005-12-15 2011-11-29 Kimberly-Clark Worldwide, Inc. Color changing cleansing composition
US8658145B2 (en) 2006-03-06 2014-02-25 The Lubrizol Corporation Low molecular weight ampholytic polymers for personal care applications
US20090291053A1 (en) * 2006-03-06 2009-11-26 Sabelko Jobiah J Low molecular weight ampholytic polymers for personal care applications
US20070238631A1 (en) * 2006-04-07 2007-10-11 Colgate-Palmolive Company Liquid cleaning composition having low viscosity
US7470653B2 (en) 2006-04-07 2008-12-30 Colgate-Palmolive Company Liquid cleaning composition comprising an anionic/betaine surfactant mixture having low viscosity
US7449436B2 (en) 2006-04-07 2008-11-11 Colgate-Palmolive Company Liquid cleaning composition comprising an anionic/betaine surfactant mixture having low viscosity
US20080274929A1 (en) * 2007-05-01 2008-11-06 Whitekettle Wilson K Method for removing microbes from surfaces
US20090074683A1 (en) * 2007-09-14 2009-03-19 L'oreal Compositions and methods for treating keratinous substrates
US8658140B2 (en) 2007-09-14 2014-02-25 L'oreal Compositions and methods for treating keratinous substrates
EP2036536A1 (en) * 2007-09-14 2009-03-18 L'Oréal Hair treatment including the application of a polyamine and a fatty acid
EP2067467A3 (en) * 2007-09-14 2012-12-12 L'Oréal Compositions and methods for treating keratinous substrates
FR2920966A1 (en) * 2007-09-14 2009-03-20 Oreal capillary method comprising applying a polyamine and a fatty acid
US8022028B2 (en) 2008-06-17 2011-09-20 Colgate-Palmolive Company Light duty liquid cleaning compositions and methods of manufacture and use thereof comprising organic acids
US8247362B2 (en) 2008-06-17 2012-08-21 Colgate-Palmolive Company Light duty liquid cleaning compositions and methods of manufacture and use thereof
US8309504B2 (en) 2008-06-17 2012-11-13 Colgate-Palmolive Company Light duty liquid cleaning compositions and methods of manufacture and use thereof
US7718595B2 (en) 2008-06-17 2010-05-18 Colgate Palmolive Company Light duty liquid cleaning compositions and methods of manufacture and use thereof comprising organic acids
US20090312227A1 (en) * 2008-06-17 2009-12-17 Colgate-Palmolive Light duty liquid cleaning compositions and methods of manufacture and use thereof
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