Shampoo conditioner formulations

Abstract
Aqueous shampoo-conditioner formulations having good cleansing, foaming, conditioning and detangling properties are provided. These formulations contain from about 4 to 25% by weight of an amphoteric surfactant, 4.5 to 25% by weight of a cryptoanionic surfactant, and from about 0.1 to 5% by weight of a cationic surfactant.
Description

This invention relates to formulations for application to hair. It particularly relates to formulations having both the desirable cleansing and foaming properties of a shampoo and the detangling and conditioning properties of a cream rinse.
Until recently the desirable properties of both a shampoo and a cream rinse could not be provided in a single formulation, and separate shampoo and cream rinse preparations had to be used if the desirable properaties of each of these preparations were to be obtained. Claims have recently been made that a shampoo formulated to contain Polymer JR Resin, a water-soluble cationic cellulosic resin described in U.S. Pat. No. 3,472,840, possessed the desirable properties of both a shampoo and a cream rinse.
However, although such preparations do clean and condition the hair, their detangling effects leave much to be desired. At best, these preparations, which contain in addition to Polymer JR Resin, triethanolamine lauryl sulfate and lauric diethanolamide, are inefficient detanglers when compared to cream rinses used independently. Furthermore, these preparations are formulated at an alkaline pH because not only do the anionic and alkanolamide surfactants function better on the alkaline pH side, but they are chemically unstable at acid pH. It is, however, preferable to use preparations of lower alkalinity for the hair.
It is, accordingly, an object of the present invention to provide a shampoo-conditioner formulation for hair, which not only cleans and conditions the hair but also serves as an efficient detangler.
It is another object of the present invention to provide a shampoo-conditioner formulation for hair, which has good foaming properties.
It is a further object of the present invention to provide a shampoo-conditioner formulation for hair, that is stable at pH from about 3.0 to 7.1, as well as at pH's up to about 8.5.
It has now been discovered that an aqueous composition comprising an amphoteric surfactant, a cryptoanionic surfactant, and a cationic surfactant has the desirable cleansing and foaming properties of a shampoo and the conditioning and detangling properties of a cream rinse.
As amphoteric surfactants I use the MIRANOL type surfactants. These are substituted imidazolines having as substituents, a long chain fatty acid radical and radicals containing hydrophlic groups. These surfactants are described in a technical and product development data report, "The MIRANOL Amphoteric Surface Active Agents", 5th Edition, 1967, published by the Miranol Chemical Company, Inc. The preferred amphoteric surfactant is MIRANOL C2MSF wherein the long chain fatty acid radical is a coconut fatty acid and the hydrophylic groups are carboxyls.
This surfactant has the structure ##STR1##
Other suitable amphoteric surfactants include amidobetaines such a Tegobetaine C, sarcosinates such as sodium lauryl sarcosinate, and long chain N-alkyl derivatives of beta-aminopropionic acid.
Crytoanionic surfactants as described in SANDOPAN DTC, a trade bulletin of Sandoz Chemical Works, New York, New York, are compounds of the formula
R--O--(R.sub.1 O).sub.n --(CH.sub.2).sub.m --CO.sub.2 H
wherein R is along chain alkyl group, R.sub.1 is ethylene or propylene, n has a value of from about 3 to 9, and m is at least 1. In practicing the invention I prefer to use SANDOPAN DTC which is a substance of the formula
R--O--(CH.sub.2 CH.sub.2 O).sub.n --CH.sub.2 --CO.sub.2 H
wherein R contains 13 carbon atoms and n has a value of about 6.5.
Cationic surfactants are nitrogen compounds, such as quaternary ammonium compounds, betaines, amine oxides, salts of fatty amines, and the like, having surfactant properties. In the practice of this invention I prefer to use quaternary ammonium compounds. These compounds include long chain quaternary ammonium salts as, for example, stearyl-dimethyl-benzylammonium chloride, lauryl-dimethyl-benzylammonium bromide, cetyl-pyridinium chloride, and the like, and polymeric substances carrying quaternary ammonium groups. Examples of such polymeric sustances are the Polymer JR Resins and GAFQUATS.
The Polymer JR Resins are water-soluble cationic cellulose ethers having a chain of anhydroglucose units with substituent groups pendant therefrom spaced along the chain, each of said groups carrying a quaternary ammonium group. The structure and preparation of these surfactants are described in U.S. Pat. No. 3,742,840. The molecular weights of these surfactants vary over a wide range, and while all such surfactants have been found suitable in the practice of the present invention, the preferred surfactant is the JR-30M resin which has a molecular weight of about 30,000.
GAFQUATS is the trademark for quaternium-23 compounds which are copolymers of vinylpyrrolidone and diethylaminoethyl methacrylate quaternized with dimethyl sulfate. The molecular weights of these surfactants range from about 100,000 to about 1,000,000. As preferred GAFQUATS, I use GAFQUAT-734 which has a molecular weight of about 100,000 and is available as a 50% by weight solution in ethanol, and GAFQUAT-755 which has a molecular weight of about 1,000,000 and is available as a 20% by weight aqueous solution.
The aqueous compositions of the present invention are formulated to contain from about 4 to 25% by weight of the amphoteric surfactant, from about 4.5 to 25% by weight of the cryptoanionic surfactant, and from about 0.1 to 5% by weight of the cationic surfactant. If desired, additional agents such as sequestering agents, surfactants, U-V absorbents, conditioners, emolients, opacifiers, thickeners, dyes, perfumes and preservatives may be added.
The amounts of the amphoteric and cryptoanionic surfactants are adjusted so that the pH of the final formulation will be between about 3.0 to 8.5, preferably between about 6.2 and 6.9.





The invention will be more fully understood from the examples which follow. These examples are given by way of illustration and are not to be considered as limiting. In the examples the numbers refer to parts by weight. The number in parenthesis directly following an ingredient such as, for example, MIRANOL C2MSF (70), indicates that the material is present in an aqueous solution (ethanolic solution in the case of GAFQUAT-734), the number in the parenthesis referring to the percent concentration.
______________________________________Example 1Polymer JR-30M 0.5Miranol C2MSF (70) 15.0Sandopan DTC Acid (90) 21.0Water QS 100Example 2Polymer JR-30M 1.5Miranol C2MSF (70) 11.0Sandopan DTC Acid (90) 15.0Stearate Opacifier 2.0(Ethylene glycol distearate)Methyl Parasept 0.2Propyl Parasept 0.05Protein Hydrolysate 0.5Perfume Oil 0.3FDC Yellow No. 5 (2) 0.2Water QS 100Example 3Polymer Jr-400 2.0Miranol C2MSF (70) 8.0Sandopan DTC Acid (90) 11.0Ricinoleic Diethanolamide 1.0Formalin Solution 0.15Perfume Oil 0.3Water QS 100Example 4Gafquat 755 (20) 5.0Miranol C2MSF (70) 11.0Sandopan DTC Acid (90) 15.0Protein Hydorlysate 0.5Disodium EDTA 0.5Stearyl Dimethyl Amine Oxide(25% Active)Methyl Parasept 0.2Propyl Parasept 0.05Perfume Oil 0.3Water QS 100Example 5Stearyl Dimethyl Benzyl 1.0Ammonium ChlorideMiranol C2MSF (70) 11.0Sandopan DTC Acid (90) 15.0Hydroxypropyl Cellulose 1.0Formalin Solution 0.15Perfume Oil 0.3Water QS 100Example 6Polymer JR-400 1.0Coco Amido Alkyl Betaine (30) 20.0Sandopan DTC Acid (90) 5.070:30 Lauric-Myristic 5.0DiethanolamideEthoxylated Lanolin Alcohols 1.0-25 EtOFormalin Solution 0.15Perfume Oil 0.3Water QS 100Example 7Polymer JR-125 1.0N-Coco-beta-amino 5.0propionic acidSandopan DTC Acid (90) 5.0Stearyl Dimethyl Amine Oxide 2.0Coconut Monoethanolamide 5.0Propylene Glycol 3.0Dowacil 200 0.1Perfume Oil 0.3Water QS 100Example 8N-(Stearoyl-colamino-formyl- 0.5methyl)-Pyridinium ChlorideMiranol C2MSF (70) 11.0Sandopan DTC Acid (90) 15.0Polyvinylpyrrolidone-K90 5.0Dowacil 200 0.1Perfume Oil 0.3Uvinul MS-40 (UV Absorbing Agent) 0.05FDC Green No. 5 (2) 0.03Water QS 100Example 9Stearylamidopropyl diethanolamine 2.0lactateMiranol C2M-SF (70) 15.0Sandopan DTC Acid (90) 21.0Hydroxypropyl Cellulose 1.0Formalin Solution 0.1FD & C Green No. 5 (2) 0.2Water QS 100Example 10Gluconamidopropyl dimethyl 5.02-hydroxyethyl ammonium chloride(60)Sandopan DTC Acid (90) 10.0Coco Amido Alkyl Betaine (30) 15.0Miranol C2M-SF (70) 7.3Lauric Diethanolamide 2.0Disodium salt ofEthylenediaminetetraacetic Acid 0.3Methyl Parasept 0.2Propyl Parasept 0.05Perfume Oil 0.2Water QS 100Example 11GAFQUAT 734 (50) 5.0Coco Amido Propyl Dimethyl 8.0Amine Oxide (30)Sandopan DTC Acid (90) 15.0Miranol C2M-SF (70) 11.0Hydroxypropyl Cellulose 2.0Glyco Amido Stearate 3.0Dowacil 200 0.1FDC Red No. 19 (1) 0.2Water QS 100Example 12GAFQUAT 755 (20) 10.0Sandopan DTC Acid (90) 15.0Isostearylamidopropyldiethanolamine 4.0Coconut Diethanolamide 5.0Tween 20 5.0Protein Hydrolysate 1.0Dimethylol dimethyl hydantoin 0.8Water QS 100______________________________________
These formulations of these examples had pH's falling within the range of 3.0 to 8.5.
The formulations were tested on hair and were found to have excellent cleaning, foaming, conditioning and detangling properties.
Claims
  • 1. An aqueous shampoo-conditioner formulation for hair, said formulation having a pH from about 3.0 to 8.5 and containing as essential ingredients from about 4 - 25% by weight of an amphoteric surfactant of the formula ##EQU1## from about 4.5 to 25% by weight of a cryptoanionic surfactant of the formula
  • R--O--(CH.sub.2 CH.sub.2 O).sub.n --CH.sub.2 CO.sub.2 H
  • wherein R is an alkyl group having 13 carbon atoms and n has a value of about 6.5, and from 0.1 to 5% of a cationic surfactant selected from the group consisting of water-soluble cellulosic ethers having a chain of anhydroglucose units with substituent groups each carrying a quaternary ammonium group pendant from and spaced along the chain, long chain quaternary ammonium compounds, and copolymers of vinylpyrrolidone and dimethylaminoethyl methacrylate quaternized with dimethyl sulfate.
  • 2. A composition according to claim 1 wherein the pH is from about 6.2 to 6.9.
  • 3. A composition according to claim 1 wherein the cationic surfactant is a water-soluble cellulose ether having a chain of anhydroglucose units with substituent groups carrying a quaternary ammonium group pendant from and spaced along the chain.
  • 4. A composition according to claim 3 wherein the molecular weight of the water-soluble cellulose ether is about 30,000.
  • 5. A composition according to claim 4 which contans 1.5% of the cationic surfactant, 7.7% of the amphoteric surfactant, and 13.5% of the cryptoanionic surfactant.
  • 6. A composition according to claim 1 wherein the cationic surfactant is a long chain quaternary ammonium compound.
  • 7. A composition according to claim 6 wherein the long chain quaternary ammonium compound is stearyl-dimethyl-benzylammonium chloride.
  • 8. A composition according to claim 7 wherein the long chain quaternary ammonium compound is stearol-colamino-formyl-methylpyridinium chloride.
  • 9. A composition according to claim 1 wherein the cationic surfactant is a copolymer of vinylpyrrolidone and diethylaminoethyl methacrylate quaternized with dimethyl sulfate.
  • 10. A composition according to claim 9 wherein the molecular weight of the cationic surfactant is about 100,000 to 1,000,000.
Parent Case Info

This application is a continuation-in-part application of patent application Ser. No. 438,879, filed Feb. 1, 1974, now abandoned which is a continuation-in-part application of patent application Ser. No. 372,590, filed June 22, 1973, now abandoned.

US Referenced Citations (6)
Number Name Date Kind
3156656 Libby Nov 1964
3322676 Hiestand May 1967
3452042 Mannheimer Jun 1969
3472840 Stone et al. Oct 1969
3578719 Kalopissis et al. May 1971
3808329 Bolich et al. Apr 1974
Continuation in Parts (2)
Number Date Country
Parent 438879 Feb 1974
Parent 372590 Jun 1973