US3666857A - Aqueous compositions containing lanolin oil - Google Patents

Aqueous compositions containing lanolin oil Download PDF

Info

Publication number
US3666857A
US3666857A US531756A US3666857DA US3666857A US 3666857 A US3666857 A US 3666857A US 531756 A US531756 A US 531756A US 3666857D A US3666857D A US 3666857DA US 3666857 A US3666857 A US 3666857A
Authority
US
United States
Prior art keywords
lanolin
liquid fraction
present
composition
fatty acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US531756A
Inventor
Kenneth L Russell
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Henkel Corp
Malmstrom Chemical Corp
Original Assignee
Malmstrom Chemical Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Malmstrom Chemical Corp filed Critical Malmstrom Chemical Corp
Application granted granted Critical
Publication of US3666857A publication Critical patent/US3666857A/en
Anticipated expiration legal-status Critical
Assigned to HENKEL CORPORATION, A DE CORP. reassignment HENKEL CORPORATION, A DE CORP. ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: QUANTUM CHEMICAL CORPORATION
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/925Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of animal origin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/42Amides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair

Definitions

  • This invention relates to aqueous compositions containing lanolin oil, and concerns particularly aqueous compositions in which lanolin oil is employed as an emollient and conditioner component of the composition, as in the case of shampoos and other detergent products.
  • the invention is concerned with the preparation of such compositions in the form of clear, transparent aqueous solutions.
  • aqueous detergent preparations containing an appreciable quantity of lanolin were characterized by opaqueness of the product, owing to the fact that the lanolin was emulsified in the detergent solution, rather than being completely solubilized therein or at least so finely dispersed therein that the product is clear to the naked eye and exhibits a transparency thereto sufficient to look like a solution.
  • non-ionic surfactants of the polyoxyethylene ester, ether, and ether-ester types are efiicient solubilizers for oils, in that they form clear, transparent emulsions of liquid oils which are, in effect, oil in water emulsions wherein the product is clear because the particle size of the oil is so small that light is not refracted by the particles.
  • non-ionic surface active agents commonly used in cosmetic formulations are not, however, efficient solubilizers for lanolin, so that it is necessary to employ relatively high ratios of such non-ionics to lanolin, in order to solubilize the oil sufficiently to form a clear, transparent solution.
  • lanolin and fractionated lanolin are described as being rendered water-soluble by combining therewith certain higher fatty acid alkylolamides in ratios of from 1:1 to 100:1. ln practise, however, it has been found necessary to employ a ratio of at least 8:1 of alkylolamide to lanolin in order to solubilize the latter. Thus, in each of the illustrative examples set forth in the Wei patent, the ratio of alkylolamide to lanolin is 10:1.
  • the principal object of the present invention is to provide aqueous compositions which contain lanolin oil as an essential component thereof and are in the form of clear, transparent solutions.
  • Another object of the invention is to provide aqueous compositions of the character set forth, which will be of particular advantage in the preparation of hair shampoos, hand lotions and other cosmetic and pharmaceutical products.
  • the objects and advantages of the invention may be achieved by combining with lanolin oil, a non-ionic surface active agent consisting essentially of a polyoxyethylene ether of lanolin alcohols, and a higher fatty acid a1- kanolamide, and then combining this mixture with an aqueous solution of an organic synthetic detergent, or a fatty acid soap, or suitable admixtures thereof.
  • a non-ionic surface active agent consisting essentially of a polyoxyethylene ether of lanolin alcohols, and a higher fatty acid a1- kanolamide
  • the lanolin oil used in accordance with the invention is a water-insoluble liquid fraction of lanolin composed for the most part of liquid lanolin esters.
  • Typical of such lanolin oils for example, is the liquid fraction of lanolin obtained from wool grease by solvent fractionation and crystallization according to the process set forth in U.S. Pat. No. 2,758,125 to Sunde.
  • a lanolin oil of this type is commercially available from Malmstrom Chemical Corporation under the tradenarne Lantrol".
  • Other lanolin oils suitable for use in the practise of the invention are available commercially from other suppliers under the trademarks Lanogene, Fluilan" and "Viscolan.
  • the non-ionic surface active agent preferably employed as one of the components of the solubilizing agent for the lanolin oil in accordance with the invention is a polyoxyethylene ether of lanolin alcohols condensed with 16 mols of ethylene oxide. Typical of such an ether is the product marketed under the trademark Nimcolan S" by Malmstrom Chemical Corporation.
  • the alkanolamide employed as the other component of the solubilizing agent for the lanolin oil in accordance with the invention may be any of a number of well-known alkanolamides of higher fatty acids, preferably the diethenolarnide of coconut fatty acid.
  • suitable alkanolamides are those marketed by Clintwood Chemical Company under the trade designations Sandrol Superamide 100C" and by others.
  • mixtures of a lanolin alcohol polyoxyethylene oxide ether, particularly of the preferred type above-mentioned, with a higher fatty acid alkanolamide provide surprisingly effective results when employed as solubilizer for lanolin oil in the preparation of clear, transparent aqueous solutions containing lanolin oil.
  • these ingredients in admixture with one another lend themselves to use in concentrations, relative to the concentration of the lanolin oil, such as to effect a synergistic solubilization of the lanolin oil.
  • markedly lower relative amounts of these ingredients serve to produce clear, transparent aqueous solutions containing lanolin oil.
  • solubilizing mixtures of the polyoxyethylene ether of lanolin alcohols with the higher fatty acid alkanolamide may be employed in' relative proportions as hereinafter more particularly set forth, to form clear, transparent aqueous compositions containing from approximately 1 to 3 percent by weight of lanolin oil and from about 5 to 30 percent, preferably from about 8 to 24 percent, by weight, of a water-soluble detergent, such as a fatty acid soap, or a suitable ionic or non-ionic synthetic detergent, or suitable mixtures thereof.
  • aqueous solutions containing from about 8 to 24 percent triethanolamine lauryl sulfate as detergent and from 1 to 3 percent lanolin oil clear, transparent solutions may be obtained by utilizing a mixture of the polyoxyethylene ether of lanolin alcohols with the coconut fatty acid diethanolamide in amounts such that the former is present in a ratio of from about 1:1 to 3:1 relative to the amount of lanolin oil, and the latter is present in a ratio of from about $11 to about 7:1 relative to the amount of lanolin oil, the above-mentioned synergistic effect disappearing, however, when the ratio of the polyoxyethylene ether of lanolin alcohols to the lanolin oil is about 1:1 or lower.
  • the preferred procedure is to form a mixture of lanolin oil with the above-mentioned solubilizing agents, and separately, an aqueous solution of the selected detergent, the aforesaid mixture and the detergent solution each being heated to about 75 to C., whereupon the oil mixture is added to the detergent solution with stirring at the elevated temperature above-mentioned.
  • solubilization results when utilizing the non-ionic surfactant (polyoxyethylene ether of lanolin alcohols condensed with 16 mols of ethylene oxide) and the higher fatty acid alkanolamide (coconut fatty acid diethanolamide), separately, as the solubilizer for 1.0 percent lanolin oil in aqueous solutions containing varying concentrations of an anionic detergent (triethanolamine lauryl sulfate).
  • non-ionic surfactant polyoxyethylene ether of lanolin alcohols condensed with 16 mols of ethylene oxide
  • higher fatty acid alkanolamide coconut fatty acid diethanolamide
  • the detergent solution was heated to 75-80 C.
  • the mixture of lanolin oil and solubilizing material was heated to the same temperature, and then the oil mixture was added to the detergent solution with stirring at the elevated temperature.
  • Solubilization of lanolin oil in concentrations of 1.0 percent in aqueous solutions of mixtures of anionic synthetic detergents and a fatty acid soap, and utilizing mixtures of the nonionic surfactant with the diethanolamide as solubilizer is illustrated by the following example:
  • Part 1 was heated to 78 C. and Part II was added to Part I with stirring.
  • the resulting product was hazy immediately after combining them, but became sparkling clear during 5 minutes additional heating on a steam bath at 7580 C.
  • aqueous compositions containing the lanolin oil, non-ionic surfactant and coconut fatty acid diethanolamide may be utilized in the preparation of clear aqueous hair shampoos, hand lotions and other cosmetic products.
  • Table 111 sets forth the data with respect to several clear, aqueous hair shampoos.
  • compositions A and D were clear very shortly after combining the ingredients; composition B required 5 minutes additional heating at 75-80 C.; and composition C required minutes at this temperature.
  • the product of the composition listed in Column D of Table 111 was subjected to rabbit-eye irritation tests by the Draize technique.
  • Nine rabbits were used, three with no rinsing after instillation of the product, three with rinsing after 2 seconds, three after 4 seconds.
  • In all nine rabbits zero readings for irritation of the cornea-or iris were obtained.
  • Low readings for irritation of the conjunctivae were obtained on the three rabbits eyes which were not rinsed; these readings became zero after 4 days.
  • Zero readings of conjunctivae irritation were obtained on the other six rabbits.
  • composition D listed in Table 111 was also tested for shampoo results by the so-called half-head shampoo test.
  • the hair is wetted, parted in the middle, and then the hair on one side of the part is shampooed with the product under test, and the hair on the other side of the part is shampooed with another shampoo for comparison.
  • Equal quantities of the product under test and of the reference product are used, and a trained beauty operator conducts the tests, making observations with respect to the foaming properties, feel of the hair during and after shampooing and rinsing, and combing properties of the hair on each side of the parted hair after the shampooing is completed.
  • composition D (with an addition of 0.4 percent, by weight, of a suitable perfume) was compared with several commercially available shampoo products, containing 1.0 lanolin oil and one or the other of the above-mentioned solubilizing ingredients.
  • the tests showed that the product of composition D foamed excellently and had unusually good effects on the combing properties of the hair following the shampoo. On hair damaged by bleaching or dyeing, the easier combing properties and manageability of the hair were outstandingly better when shampooed with the product of composition D than when shampooed with the commercial shampoo products tested.
  • the preferred type of alkanolamide for use in preparing the compositions of the invention is coconut fatty acid diethanolamide. More specifically, as in the compositions shown in Table 111, the diethanolamide is a 1:1 coconut fatty acid-diethanolamine condensate of high (minimum 90 percent) amide content. Thus, with this amide,
  • one lot of the non-ionic may solubilize the lanolin oil in a given detergent solution when present at a ratio of 3.0 parts to 1.0 part of lanolin oil, while another lot may require a slightly higher ratio. Similar variations occur using different lots of the fatty acid diethanolamide. Likewise, using given lots of the nonionic and the diethanolamide, one lot of lanolin oil may be slightly easier to solubilize than another. Generally the differences in the materials are small, and their effect on solubiliza'tion can be compensated for by variation of the period of heating at 7580 C.
  • the raw materials from different suppliers may also vary somewhat in their ability to solubilize, or in the case of lanolin oil, to be solubilized. However, for a given finished product, the formulator may readily determine and choose a final composition and conditions so that these variations will not be significant.
  • suitable amounts of various additive agents may be included in the final compositions embodying the invention.
  • coloring agents perfumes, dyes, preservatives, and the like.
  • diethanolamide component in the compositions of the invention serve also as foam builders or foam stabilizers in products such as shampoos, and as viscosity adjusting agents in detergent solutions.
  • composition consisting essentially of:
  • water 2. a water-soluble substance selected from the group consisting of fatty acid soaps, synthetic detergents and mixtures thereof,
  • non-ionic surfactant consisting essentially of a polyoxyethylene ether of lanolin alcohol condensed with 16 mols of ethylene oxide;
  • a higher fatty acid alkanolamide said surfactant being present in a ratio of from about 1:1 to about 3:1 relative to the amount of said liquid fraction of lanolin, and said alkanolamide being present in a ratio of from about xzl to about 7:1 relative to the amount of said liquid fraction of lanolin, whereby to effect synergistic solubilization of said liquid fraction of lanolin said composition being clear and transparent as initially produced and without requiring filtration thereof.
  • composition of claim 1 wherein said water-soluble substance is present in a concentration of from about 5 to 30 percent by weight of said solution, and wherein said liquid fraction of lanolin is present in a concentration of from approximately 1 to 3 percent by weight.
  • composition of claim 3 wherein said water-soluble substance is present in a concentration of from about 8 to 24 percent by weight of said solution, and wherein said liquid fraction of lanolin is present in a concentration of from approximately 1 to 3 percent by weight.
  • composition of claim 2 wherein said alkanolamide is a diethanolamide of coconut oil fatty acid.
  • composition of claim 3 wherein said liquid fraction of lanolin is present in a concentration of approximately 1 percent by weight, said nonionic surfactant is present in a concentration of from approximately 2 to 3 percent by weight, and said alkanolamide is a diethanolamide of coconut oil fatty acid, present in a concentration of from approximately 0.5 to
  • a composition consisting essentially of: 1. water 2. a water-soluble substance selected from the group consisting of fatty acid soaps, synthetic detergent and mixtures thereof, 3. a liquid fraction of lanolin 4. a non-ionic surfactant consisting essentially of a polyoxyethylene ether of lanolin alcohol condensed with 16 mols of ethylene oxide, and 5.
  • liquid fraction of lanolin being present in a concentration of from 1 to 3% by weight of the composition, said surfactant being present in a ratio of from about 1:1 to about 3:1 relative to the amount of said liquid fraction of lanolin, and said alkanolamide being present in a ratio of from about ;&:1 to about 7:1 relative to the amount of said liquid fraction of lanolin, whereby to effect complete solubilization of said liquid fraction of lanolin said composition being clear and transparent as initially produced and without requiring filtration thereof.
  • a liquid composition consisting essentially of:
  • a non-ionic surfactant consisting essentially of a polyoxyethylene ether made by condensing lanolin alcohols with 16 mols of ethylene oxide;
  • a higher fatty acid alkanolamide said surfactant and said alkanolamide each being present in ratios relative to the amount of said liquid fraction of lanolin to effect synergistic solubilization of said liquid fraction of lanolin, said ratio of said surfactant to said liquid fraction of lanolin being from about lzl to about 3:1, and said ratio of said alkanolamide to said liquid fraction of lanolin being from about :1 to about 7:1 said composition being clear and transparent as initially produced and without requiring filtration thereof.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Zoology (AREA)
  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Cosmetics (AREA)
  • Detergent Compositions (AREA)

Abstract

A liquid fraction of lanolin is solubilized in water with a combination of (A) fatty acid soaps and/or synthetic detergents, (B) a polyoxyethylene ether of lanolin alcohol condensed with 16 mols of ethylene oxide, and (C) a higher fatty acid alkanolamide.

Description

O E Unite States mm [is] 3,666,857 Russell May 30, 1972 [54] AQUEOUS COWOSITIONS OTHER PUBUCATlONS CONTAIN N LAN L N OIL Conrad et 211., Proceedings of Scientific Section, Toilet Goods Assoc., No.29, pages 14- I8,.Iune 1958 [72] lnvemor' Kenneth Russell Nufley Robinson, Wagner Co., Inc. Products Bulletin No. 37, pages [73] Assignee: Malmstrom Chemical Corp., Linden, NJ. 3, P 1956 Russell et al., Drug and Cosmetic Industry, Vol. 90, No. 3, Flledi 4, 1966 pages 294- 296, 325, 326, and 328, Mar. 1962 [21] Appl. No.: 531,756 Primary ExaminerRichard L. Hufi Related U.S. Application Data [63] Continuation of Ser. No. 178,221, Mar. 1, I962, aban- [57] ABSTRACT doned' A liquid fraction of lanolin is solubilized in water with a combination of (A) fatty acid soaps and/or synthetic detergents, [52] US. Cl... ..424/240, 424/70 (B) a polyoxyethylene ether Oflanolin alcohol condensed with [Sl] IIlLCl. 1 ..A61k7/08 16 mols of ethylene oxide, and a ig f y acid [58] Field of Search 167/63 L; 424/240 k l 'd [56] References Cited 7 Claims, N0 Drawings UNITED STATES PATENTS 2,900,307 8/1959 Wei ..167/63 AQUEOUS COMPOSITIONS CONTAINING LANOLIN OIL This application is a continuation of my prior application, Ser. No. 178,221, filed Mar. 1, 1962, now abandoned.
This invention relates to aqueous compositions containing lanolin oil, and concerns particularly aqueous compositions in which lanolin oil is employed as an emollient and conditioner component of the composition, as in the case of shampoos and other detergent products.
Still more particularly, the invention is concerned with the preparation of such compositions in the form of clear, transparent aqueous solutions.
Prior to relatively recent years, aqueous detergent preparations containing an appreciable quantity of lanolin were characterized by opaqueness of the product, owing to the fact that the lanolin was emulsified in the detergent solution, rather than being completely solubilized therein or at least so finely dispersed therein that the product is clear to the naked eye and exhibits a transparency thereto sufficient to look like a solution.
It is known (W.C. Griffin, Cosmetics, Science and Technology", lnterscience Publishers, lnc., New York, Sept. 16, 1957, pages 1027-1028) that non-ionic surfactants of the polyoxyethylene ester, ether, and ether-ester types are efiicient solubilizers for oils, in that they form clear, transparent emulsions of liquid oils which are, in effect, oil in water emulsions wherein the product is clear because the particle size of the oil is so small that light is not refracted by the particles. The non-ionic surface active agents commonly used in cosmetic formulations are not, however, efficient solubilizers for lanolin, so that it is necessary to employ relatively high ratios of such non-ionics to lanolin, in order to solubilize the oil sufficiently to form a clear, transparent solution.
It is also known (Conrad, Motiuk and Maso, Solubilization by Lanolin Derivatives, Proceedings of Scientific Section, Toilet Goods Association, 29, June 14, 1958) that the U.S.P. lanolin and a liquid lanolin may be solubilized by the polyoxyethylene ethers of lanolin alcohol, particularly the ether made by condensing lanolin alcohols with 16 mols of ethylene oxide.
In U.S. Pat. No. 2,900,307, to Ling Wei, dated Aug. 18, 1959, lanolin and fractionated lanolin are described as being rendered water-soluble by combining therewith certain higher fatty acid alkylolamides in ratios of from 1:1 to 100:1. ln practise, however, it has been found necessary to employ a ratio of at least 8:1 of alkylolamide to lanolin in order to solubilize the latter. Thus, in each of the illustrative examples set forth in the Wei patent, the ratio of alkylolamide to lanolin is 10:1.
The principal object of the present invention is to provide aqueous compositions which contain lanolin oil as an essential component thereof and are in the form of clear, transparent solutions.
Another object of the invention is to provide aqueous compositions of the character set forth, which will be of particular advantage in the preparation of hair shampoos, hand lotions and other cosmetic and pharmaceutical products.
Still other objects, and the advantages of, the invention will be apparent to those skilled in the art from the following more detailed description.
Briefly stated, the objects and advantages of the invention may be achieved by combining with lanolin oil, a non-ionic surface active agent consisting essentially of a polyoxyethylene ether of lanolin alcohols, and a higher fatty acid a1- kanolamide, and then combining this mixture with an aqueous solution of an organic synthetic detergent, or a fatty acid soap, or suitable admixtures thereof.
The lanolin oil used in accordance with the invention is a water-insoluble liquid fraction of lanolin composed for the most part of liquid lanolin esters. Typical of such lanolin oils, for example, is the liquid fraction of lanolin obtained from wool grease by solvent fractionation and crystallization according to the process set forth in U.S. Pat. No. 2,758,125 to Sunde. A lanolin oil of this type is commercially available from Malmstrom Chemical Corporation under the tradenarne Lantrol". Other lanolin oils suitable for use in the practise of the invention are available commercially from other suppliers under the trademarks Lanogene, Fluilan" and "Viscolan.
The non-ionic surface active agent preferably employed as one of the components of the solubilizing agent for the lanolin oil in accordance with the invention is a polyoxyethylene ether of lanolin alcohols condensed with 16 mols of ethylene oxide. Typical of such an ether is the product marketed under the trademark Nimcolan S" by Malmstrom Chemical Corporation.
The alkanolamide employed as the other component of the solubilizing agent for the lanolin oil in accordance with the invention may be any of a number of well-known alkanolamides of higher fatty acids, preferably the diethenolarnide of coconut fatty acid. Typical of suitable alkanolamides are those marketed by Clintwood Chemical Company under the trade designations Sandrol Superamide 100C" and by others.
It has been found that mixtures of a lanolin alcohol polyoxyethylene oxide ether, particularly of the preferred type above-mentioned, with a higher fatty acid alkanolamide, provide surprisingly effective results when employed as solubilizer for lanolin oil in the preparation of clear, transparent aqueous solutions containing lanolin oil. Moreover, it has been found that although the aforementioned components of the solubilizing mixture may be used in a relatively wide range of concentrations for the preparation of such aqueous products, these ingredients in admixture with one another lend themselves to use in concentrations, relative to the concentration of the lanolin oil, such as to effect a synergistic solubilization of the lanolin oil. Thus, markedly lower relative amounts of these ingredients serve to produce clear, transparent aqueous solutions containing lanolin oil.
The clarity and transparency of these solutions are an as is characteristic thereof, i.e., as produced without requiring filtering of the solutions. Hence, the terms clear" and trans parent" as used herein with reference to the solutions embodying the present invention, refer to and mean the aforesaid characteristic of the solutions as initially produced, without requiring them to be filtered to render them clear and transparent.
The herein described solubilizing mixtures of the polyoxyethylene ether of lanolin alcohols with the higher fatty acid alkanolamide may be employed in' relative proportions as hereinafter more particularly set forth, to form clear, transparent aqueous compositions containing from approximately 1 to 3 percent by weight of lanolin oil and from about 5 to 30 percent, preferably from about 8 to 24 percent, by weight, of a water-soluble detergent, such as a fatty acid soap, or a suitable ionic or non-ionic synthetic detergent, or suitable mixtures thereof.
Thus, in the case of aqueous solutions containing from about 8 to 24 percent triethanolamine lauryl sulfate as detergent and from 1 to 3 percent lanolin oil, clear, transparent solutions may be obtained by utilizing a mixture of the polyoxyethylene ether of lanolin alcohols with the coconut fatty acid diethanolamide in amounts such that the former is present in a ratio of from about 1:1 to 3:1 relative to the amount of lanolin oil, and the latter is present in a ratio of from about $11 to about 7:1 relative to the amount of lanolin oil, the above-mentioned synergistic effect disappearing, however, when the ratio of the polyoxyethylene ether of lanolin alcohols to the lanolin oil is about 1:1 or lower.
In producing the aqueous compositions according to the invention, the preferred procedure is to form a mixture of lanolin oil with the above-mentioned solubilizing agents, and separately, an aqueous solution of the selected detergent, the aforesaid mixture and the detergent solution each being heated to about 75 to C., whereupon the oil mixture is added to the detergent solution with stirring at the elevated temperature above-mentioned.
In order to demonstrate the beneficial efiects of the combination of the above-mentioned ingredients as solubilizers for lanolin oil, there is set forth in Table 1, below, the solubilization results when utilizing the non-ionic surfactant (polyoxyethylene ether of lanolin alcohols condensed with 16 mols of ethylene oxide) and the higher fatty acid alkanolamide (coconut fatty acid diethanolamide), separately, as the solubilizer for 1.0 percent lanolin oil in aqueous solutions containing varying concentrations of an anionic detergent (triethanolamine lauryl sulfate).
TABLE I.SOLUBILIZATION RESULTS 1.0% Lanolin Oil in Triethanolamlne Lauryl Sulfate Percent Trlethanolarnlne lauryl sulfate Materials 8. 16. 0 24. 0
Rntlo-nonionlc to lanolin LOzl, clcar 3.521, clear"... 3.511, clear. oi 3.15:1,cloudy... 3.0:1, cloudy 3.011, hazy. Ratio-diethanolamide to 8.11:1, clean... 8.021, clean... 9.011, clear.
lanolin oil. 7.0:1, 7.0:1, cloudy 8.11 21, cloudycloudy..-
ln contrast to the results obtained with the individual ingredients of the solubilizer, as set forth in Table 1, there are set forth in Table 11, below, the results obtained when utilim'ng mixtures of the above-mentioned ingredients as solubilizers for the lanolin oil in accordance with the invention.
TABLE ll SOLUBILIZATION RESULTS 1.0% Lanolin Oil in Triethanolamine Lauryl Sulfate Triethanolarnine In all instances set forth in Table ll, as well as in Table I, the amount of the detergent solution of triethanolamine lauryl sulfate used was 100.0 parts, less the 1.0 part of the lanolin oil and less the parts of non-ionic surfactant and the diethanolamide used, as the case may be, yielding 100.0 parts of the final composition containing 1.0 part of lanolin oil.
In all instances, also, the detergent solution was heated to 75-80 C., the mixture of lanolin oil and solubilizing material was heated to the same temperature, and then the oil mixture was added to the detergent solution with stirring at the elevated temperature.
By comparing the data set forth in Table l with those set forth in Table II, it will be noted that whereas in the case of an 8.0 percent solution of the detergent, 4.0 parts of the nonionic surfactant were required to solubilize 1.0 part of lanolin oil in 95.0 parts of the 8.0 percent detergent solution, and 8.0 parts of the diethanolamide were required to solubilize 1.0 part of lanolin oil in 91.0 parts of the 8.0 percent detergent solutions, only 3.0 parts of the nonionic surfactant and only 0.5 parts of the diethanolamide, when these two are used in admixture with one another, are required to solubilize 1.0 part of lanolin oil in 95.5 parts of the 8.0 percent detergent solution. Similarly, only 2.0 parts of the non-ionic surfactant admixed with only 2.0 parts of the diethanolamide are required to solubilize 1.0 part of lanolin oil in 96.0 parts of the 8.0 percent detergent solution. Comparably striking differences in the solubilization results will be noted when comparing the data in Table l with those of Table II in respect of the 16 and 24 percent detergent solutions.
In most instances set forth in Table II, the solubilization took place readily as the mixture of lanolin oil, non-ionic and diethanolamide, heated to 75-85 C., was added to the detergent solution heated to the same temperature. in the case of combinations made with 1.0 part of the non-ionic surfactant to 1.0 part of lanolin oil, holding the mixture of lanolin oil, non-ionic and diethanolamide with the detergent solution at a temperature of 75-80 C., for a period of up to 30 minutes may be required in order to obtain a clear, transparent solution. Indeed, in such instances, maintaining the mixture at the temperature mentioned for periods longer than 30 minutes permits the use of a smaller quantity of the diethanolamide than those shown in Table 11 for obtaining clear solutions.
As will be observed from the data in Table 11, when ratios of 3:1 and2:l of the non-ionic surfactant to lanolin oil are used, the amount of diethanolamide required for solubilization is substantially less than would be calculated if the solubility effects of the non-ionic and diethanolamide were merely additive. This synergistic solubilization of the lanolin oil is exemplified in the compositions of series (A) and (B) in Table 11. This synergistic effect disappears, apparently, when the ratio of non-ionic to lanolin oil is 1:1.
Using mixtures of the non-ionic and diethanolamide, larger quantities of lanolin oil were readily solubilized. For example, the following two compositions containing 3.0 percent lanolin oil were clear immediately after combining the ingredients by the above-mentioned procedure:
Triethanolamine Lauryl Sulfate 16.0 16.0
Water 57.0 58.0
Non-ionic (lanolin alcohols with 16 mols ethylene oxide) 9.0 10.5
Lanolin Oil 3.0 3.0
Coconut Fatty Acid Diethanolamide 15.0 12.0 Total: 100.0 100.0
Solubilization of lanolin oil in aqueous solutions of detergents other than the one referred to in Tables 1 and II, when utilizing mixtures of the non-ionic and diethanolamide as solubilizers, resulting in clear, transparent solutions, is illustrated by the two following examples of compositions prepared in the manner above set forth:
Sodium Lauryl Polyoxyethylene Ether l 2 Sulfate 1 2.0
Triethanolamine Dodecyl Benzene Sulfonate 124 Water 79.0 78.1
Non-ionic (lanolin alcohols with 16 mols ethylene oxide) 20 2.5
Lanolin oil 1.0 1.0
Coconut Fatty Acid Diethanolamide 6.0 6.0 Total: 100.0 100.0
Solubilization of lanolin oil in concentrations of 1.0 percent in aqueous solutions of mixtures of anionic synthetic detergents and a fatty acid soap, and utilizing mixtures of the nonionic surfactant with the diethanolamide as solubilizer, is illustrated by the following example:
Part I Parts Sodium lauryl sulfate 9.0 Triethanolamine dodecyl benzene sulfonate Potassium Oleate 2.5 Water 72.0
Part I] Non-ionic (lanolin alcohols with 16 mols ethylene oxide) 2.5
Lanolin oil 1.0
Coconut fatty acid diethanolamide 5.0 Total: 100.0
Part 1 was heated to 78 C. and Part II was added to Part I with stirring. The resulting product was hazy immediately after combining them, but became sparkling clear during 5 minutes additional heating on a steam bath at 7580 C.
As above indicated, the aqueous compositions containing the lanolin oil, non-ionic surfactant and coconut fatty acid diethanolamide, may be utilized in the preparation of clear aqueous hair shampoos, hand lotions and other cosmetic products. Table 111, below, sets forth the data with respect to several clear, aqueous hair shampoos.
TABLE I11 SHAMPOO A B C D Triethanolamine lauryl 12.0 12.0 12.0 12.0 Sulfate Triethanolamine oleate 5.0 5.0 5.0 5.0 Propylene glycol 5.0 5.0 5.0 5.0 Water 71.0 70.5 69.0 69.0 Lanolin oil 1.0 1.0 1.0 1.0 Lanolin alcohols condensed with 16 mols of ethylene oxide 3.0 2.5 2.0 3.0 Coconut fatty acid 1:1 diethanolamide 3.0 4.0 6.0 5.0
Total: 100.0 100.0 100.0 100.0
The anionic detergent, soap and propylene glycol were dissolved in the water and this solution heated to 7580 C. The other ingredients were combined and heated to the same temperature, then poured into the aqueous solution while stirring. Compositions A and D were clear very shortly after combining the ingredients; composition B required 5 minutes additional heating at 75-80 C.; and composition C required minutes at this temperature.
Although the data in Table 111, above, indicate that the synergistic effect of the non-ionic and the diethanolamide is not exerted, it is believed this is due to the presence of the propylene glycol, and that in the absence of the latter the synergistic effect would be exerted.
The product of the composition listed in Column D of Table 111 was subjected to rabbit-eye irritation tests by the Draize technique. Nine rabbits were used, three with no rinsing after instillation of the product, three with rinsing after 2 seconds, three after 4 seconds. In all nine rabbits zero readings for irritation of the cornea-or iris were obtained. Low readings for irritation of the conjunctivae were obtained on the three rabbits eyes which were not rinsed; these readings became zero after 4 days. Zero readings of conjunctivae irritation were obtained on the other six rabbits.
The product of composition D listed in Table 111 was also tested for shampoo results by the so-called half-head shampoo test. In such test, the hair is wetted, parted in the middle, and then the hair on one side of the part is shampooed with the product under test, and the hair on the other side of the part is shampooed with another shampoo for comparison. Equal quantities of the product under test and of the reference product are used, and a trained beauty operator conducts the tests, making observations with respect to the foaming properties, feel of the hair during and after shampooing and rinsing, and combing properties of the hair on each side of the parted hair after the shampooing is completed. Utilizing this test, the product of composition D (with an addition of 0.4 percent, by weight, of a suitable perfume) was compared with several commercially available shampoo products, containing 1.0 lanolin oil and one or the other of the above-mentioned solubilizing ingredients. The tests showed that the product of composition D foamed excellently and had unusually good effects on the combing properties of the hair following the shampoo. On hair damaged by bleaching or dyeing, the easier combing properties and manageability of the hair were outstandingly better when shampooed with the product of composition D than when shampooed with the commercial shampoo products tested.
As hereinbefore indicated, the preferred type of alkanolamide for use in preparing the compositions of the invention is coconut fatty acid diethanolamide. More specifically, as in the compositions shown in Table 111, the diethanolamide is a 1:1 coconut fatty acid-diethanolamine condensate of high (minimum 90 percent) amide content. Thus, with this amide,
a clear, transparent product is obtained immediately after combining the following ingredients, in the proportions indicated, at 75 to C. in the manner above set forth:
Triethanolamine lauryl sulfate 8.0
Water 87.0
Polyoxyethylene ether (lanolin alcohols with 16 mols ethylene oxide) 2.0
Lanolin oil 1.0
Amide 2.0 Total: 100.0
Experiments have shown that different lots of raw materials may produce some variation in results. For example, one lot of the non-ionic may solubilize the lanolin oil in a given detergent solution when present at a ratio of 3.0 parts to 1.0 part of lanolin oil, while another lot may require a slightly higher ratio. Similar variations occur using different lots of the fatty acid diethanolamide. Likewise, using given lots of the nonionic and the diethanolamide, one lot of lanolin oil may be slightly easier to solubilize than another. Generally the differences in the materials are small, and their effect on solubiliza'tion can be compensated for by variation of the period of heating at 7580 C. The raw materials from different suppliers may also vary somewhat in their ability to solubilize, or in the case of lanolin oil, to be solubilized. However, for a given finished product, the formulator may readily determine and choose a final composition and conditions so that these variations will not be significant.
As will be understood by those skilled in the an, suitable amounts of various additive agents may be included in the final compositions embodying the invention. Among these are coloring agents, perfumes, dyes, preservatives, and the like. In this connection, it is noteworthy that the diethanolamide component in the compositions of the invention serve also as foam builders or foam stabilizers in products such as shampoos, and as viscosity adjusting agents in detergent solutions.
- What is claimed is:
1. A composition consisting essentially of:
1. water 2. a water-soluble substance selected from the group consisting of fatty acid soaps, synthetic detergents and mixtures thereof,
3. a liquid fraction of lanolin,
4. a non-ionic surfactant consisting essentially of a polyoxyethylene ether of lanolin alcohol condensed with 16 mols of ethylene oxide; and
5. a higher fatty acid alkanolamide: said surfactant being present in a ratio of from about 1:1 to about 3:1 relative to the amount of said liquid fraction of lanolin, and said alkanolamide being present in a ratio of from about xzl to about 7:1 relative to the amount of said liquid fraction of lanolin, whereby to effect synergistic solubilization of said liquid fraction of lanolin said composition being clear and transparent as initially produced and without requiring filtration thereof.
2. The composition of claim 1, wherein said water-soluble substance is present in a concentration of from about 5 to 30 percent by weight of said solution, and wherein said liquid fraction of lanolin is present in a concentration of from approximately 1 to 3 percent by weight.
3. The composition of claim 1, wherein said water-soluble substance is present in a concentration of from about 8 to 24 percent by weight of said solution, and wherein said liquid fraction of lanolin is present in a concentration of from approximately 1 to 3 percent by weight.
4. The composition of claim 2, wherein said alkanolamide is a diethanolamide of coconut oil fatty acid.
5. The composition of claim 3, wherein said liquid fraction of lanolin is present in a concentration of approximately 1 percent by weight, said nonionic surfactant is present in a concentration of from approximately 2 to 3 percent by weight, and said alkanolamide is a diethanolamide of coconut oil fatty acid, present in a concentration of from approximately 0.5 to
3 percent by weight, the lower the concentration of said nonionic surfactant the higher the concentration of said diethanolamide.
6. A composition consisting essentially of: 1. water 2. a water-soluble substance selected from the group consisting of fatty acid soaps, synthetic detergent and mixtures thereof, 3. a liquid fraction of lanolin 4. a non-ionic surfactant consisting essentially of a polyoxyethylene ether of lanolin alcohol condensed with 16 mols of ethylene oxide, and 5. a diethanolamide of coconut oil fatty acid; said liquid fraction of lanolin being present in a concentration of from 1 to 3% by weight of the composition, said surfactant being present in a ratio of from about 1:1 to about 3:1 relative to the amount of said liquid fraction of lanolin, and said alkanolamide being present in a ratio of from about ;&:1 to about 7:1 relative to the amount of said liquid fraction of lanolin, whereby to effect complete solubilization of said liquid fraction of lanolin said composition being clear and transparent as initially produced and without requiring filtration thereof.
7. A liquid composition consisting essentially of:
a. water b. a liquid fraction of lanolin,
c. a non-ionic surfactant consisting essentially of a polyoxyethylene ether made by condensing lanolin alcohols with 16 mols of ethylene oxide; and
d. a higher fatty acid alkanolamide; said surfactant and said alkanolamide each being present in ratios relative to the amount of said liquid fraction of lanolin to effect synergistic solubilization of said liquid fraction of lanolin, said ratio of said surfactant to said liquid fraction of lanolin being from about lzl to about 3:1, and said ratio of said alkanolamide to said liquid fraction of lanolin being from about :1 to about 7:1 said composition being clear and transparent as initially produced and without requiring filtration thereof.
I t 0* i

Claims (14)

  1. 2. a water-soluble substance selected from the group consisting of fatty acid soaps, synthetic detergents and mixtures thereof,
  2. 2. The composition of claim 1, wherein said water-soluble substance is present in a concentration of from about 5 to 30 percent by weight of said solution, and wherein said liquid fraction of lanolin is present in a concentration of from approximately 1 to 3 percent by weight.
  3. 2. a water-soluble substance selected from the group consisting of fatty acid soaps, synthetic detergent and mixtures thereof,
  4. 3. a liquid fraction of lanolin
  5. 3. The composition of claim 1, wherein said water-soluble substance is present in a concentration of from about 8 to 24 percent by weight of said solution, and wherein said liquid fraction of lanolin is present in a concentration of from approximately 1 to 3 percent by weight.
  6. 3. a liquid fraction of lanolin,
  7. 4. a non-ionic surfactant consisting essentially of a polyoxyethylene ether of lanolin alcohol condensed with 16 mols of ethylene oxide; and
  8. 4. The composition of claim 2, wherein said alkanolamide is a diethanolamide of coconut oil fatty acid.
  9. 4. a non-ionic surfactant consisting essentially of a polyoxyethylene ether of lanolin alcohol condensed with 16 mols of ethylene oxide, and
  10. 5. a diethanolamide of coconut oil fatty acid; said liquid fraction of lanolin being present in a concentration of from 1 to 3% by weight of the composition, said surfactant being present in a ratio of from about 1:1 to about 3:1 relative to the amount of said liquid fraction of lanolin, and said alkanolamide being present in a ratio of from about 1/2 :1 to about 7:1 relative to the amount of said liquid fraction of lanolin, whereby to effect complete solubilization of said liquid fraction of lanolin said composition being clear and transparent as initially produced and without requiring filtration thereof.
  11. 5. The composition of claim 3, wherein said liquid fraction of lanolin is present in a concentration of approximately 1 percent by weight, said non-ionic surfactant is present in a concentration of from approximately 2 to 3 percent by weight, and said alkanolamide is a diethanolamide of coconut oil fatty acid, present in a concentration of from approximately 0.5 to 3 percent by weight, the lower the concentration of said non-ionic surfactant the higher the concentration of said diethanolamide.
  12. 5. a higher fatty acid alkanolamide: said surfactant being present in a ratio of from about 1:1 to about 3:1 relative to the amount of said liquid fraction of lanolin, and said alkanolamide being present in a ratio of from about 1/2 :1 to about 7:1 relative to the amount of said liquid fraction of lanolin, whereby to effect synergistic solubilization of said liquid fraction of lanolin said composition being clear and transparent as initially produced and without requiring filtration thereof.
  13. 6. A composition consisting essentially of:
  14. 7. A liquid composition consisting essentially of: a. water b. a liquid fraction of lanolin, c. a non-ionic surfactant consisting essentially of a polyoxyethylene ether made by condensing lanolin alcohols with 16 mols of ethylene oxide; and d. a higher fatty acid alkanolamide; said surfactant and said alkanolamide each being present in ratios relative to the amount of said liquid fraction of lanolin to effect synergistic solubilization of said liquid fraction of lanolin, said ratio of said surfactant to said liquid fraction of lanolin being from about 1:1 to about 3:1, and said ratio of said alkanolamide to said liquid fraction of lanolin being from about 1/2 :1 to about 7:1 said composition being clear and transparent as initially produced and without requiring filtration thereof.
US531756A 1966-03-04 1966-03-04 Aqueous compositions containing lanolin oil Expired - Lifetime US3666857A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US53175666A 1966-03-04 1966-03-04

Publications (1)

Publication Number Publication Date
US3666857A true US3666857A (en) 1972-05-30

Family

ID=24118923

Family Applications (1)

Application Number Title Priority Date Filing Date
US531756A Expired - Lifetime US3666857A (en) 1966-03-04 1966-03-04 Aqueous compositions containing lanolin oil

Country Status (1)

Country Link
US (1) US3666857A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4279262A (en) * 1973-04-09 1981-07-21 Kao Soap Co., Ltd. Hair treating agent of the pre-shampoo type
FR2525627A1 (en) * 1982-04-23 1983-10-28 Thorel Jean IMPROVEMENTS IN LIPID CLEANING AND RESTORATION PROCESSES AND PRODUCTS FOR THEIR IMPLEMENTATION
EP0217250A2 (en) * 1985-09-28 1987-04-08 Henkel Kommanditgesellschaft auf Aktien Foaming surfactant preparations with clear, solubilized water insoluble oil components
US4960592A (en) * 1989-04-17 1990-10-02 Lanocare Laboratories Lanolin and lanolin oil skin treatment composition
WO1998047468A1 (en) * 1997-04-22 1998-10-29 Woolcombers Group Plc Aqueous compositions comprising a lipid and a lanolin-derived surfactant, and their use
US7220712B1 (en) 2002-03-04 2007-05-22 Maggi Anthony G Compositions and methods for cleaning and conditioning
US20110003888A1 (en) * 2007-01-12 2011-01-06 Bioactives, Inc. Hops extraction methods and mixtures

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2900307A (en) * 1957-07-05 1959-08-18 Colgate Palmolive Co Clear liquid solubilized lanolin compositions

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2900307A (en) * 1957-07-05 1959-08-18 Colgate Palmolive Co Clear liquid solubilized lanolin compositions

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
Conrad et al., Proceedings of Scientific Section, Toilet Goods Assoc., No. 29, pages 14 18, June 1958 *
Robinson, Wagner Co., Inc. Products Bulletin No. 37, pages 2 3, Apr. 2, 1956 *
Russell et al., Drug and Cosmetic Industry, Vol. 90, No. 3, pages 294 296, 325, 326, and 328, Mar. 1962 *

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4279262A (en) * 1973-04-09 1981-07-21 Kao Soap Co., Ltd. Hair treating agent of the pre-shampoo type
FR2525627A1 (en) * 1982-04-23 1983-10-28 Thorel Jean IMPROVEMENTS IN LIPID CLEANING AND RESTORATION PROCESSES AND PRODUCTS FOR THEIR IMPLEMENTATION
EP0093033A1 (en) * 1982-04-23 1983-11-02 Jean-Noel Thorel Processes for cleaning and lipidic restoration, and products therefor
EP0217250A2 (en) * 1985-09-28 1987-04-08 Henkel Kommanditgesellschaft auf Aktien Foaming surfactant preparations with clear, solubilized water insoluble oil components
EP0217250A3 (en) * 1985-09-28 1988-03-23 Henkel Kommanditgesellschaft Auf Aktien Foaming surfactant preparations with clear, solubilized water insoluble oil components
US4960592A (en) * 1989-04-17 1990-10-02 Lanocare Laboratories Lanolin and lanolin oil skin treatment composition
WO1998047468A1 (en) * 1997-04-22 1998-10-29 Woolcombers Group Plc Aqueous compositions comprising a lipid and a lanolin-derived surfactant, and their use
GB2334446A (en) * 1997-04-22 1999-08-25 Woolcombers Group Plc Aqueous compositions compromising a lipid and a lanolin-derived surfactant,and their use
US6224853B1 (en) * 1997-04-22 2001-05-01 Woolcombers Group Plc Aqueous compositions comprising a lipid and a lanolin-derived surfactant, and their use
GB2334446B (en) * 1997-04-22 2002-01-09 Woolcombers Group Plc Aqueous compositions compromising a lipid and a lanolin-derived surfactant,and their use
US7220712B1 (en) 2002-03-04 2007-05-22 Maggi Anthony G Compositions and methods for cleaning and conditioning
US20110003888A1 (en) * 2007-01-12 2011-01-06 Bioactives, Inc. Hops extraction methods and mixtures

Similar Documents

Publication Publication Date Title
DE3533977C2 (en) Highly foaming nonionic surfactant-based liquid cleaner
US4654207A (en) Pearlescent shampoo and method for preparation of same
US3590122A (en) Shampoo composition
US5019376A (en) Sparkling pearlescent personal care compositions
JP2536800B2 (en) Detergent composition
US4126674A (en) Thickened aqueous shampoo compositions containing encapsulated conditioning agents
US3326808A (en) Antiseptic detergent composition
IE51356B1 (en) Liquid skin cleanser composition
US5646106A (en) Cold pearlizing concentrates
US4026825A (en) Foaming and conditioning detergent composition
US3085067A (en) Sarcosinate shampoo
US3766097A (en) Detergent (soap) compositions
US3666857A (en) Aqueous compositions containing lanolin oil
US4865757A (en) Personal hygiene preparation comprising soap and ether carboxylates
US2900307A (en) Clear liquid solubilized lanolin compositions
US4430245A (en) Soap composition
JPH01287017A (en) Low-irritant washing agent composition
US4261851A (en) Low-irritating detergent composition
KR930007227B1 (en) Balanced newtral liquid detergent lotion emulsion formulation
US2290908A (en) Shampoo
JPH0782127A (en) Cosmetic
JPH08208455A (en) Liquid cleaner
JPS61272294A (en) Detergent composition
JPS61272295A (en) Detergent composition
JP2000007554A (en) Cosmetic for cleansing

Legal Events

Date Code Title Description
AS Assignment

Owner name: HENKEL CORPORATION, A DE CORP., PENNSYLVANIA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:QUANTUM CHEMICAL CORPORATION;REEL/FRAME:005270/0484

Effective date: 19891013