US3562167A - Solid transparent detergent compositions and method of making the same - Google Patents

Solid transparent detergent compositions and method of making the same Download PDF

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US3562167A
US3562167A US591394A US3562167DA US3562167A US 3562167 A US3562167 A US 3562167A US 591394 A US591394 A US 591394A US 3562167D A US3562167D A US 3562167DA US 3562167 A US3562167 A US 3562167A
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parts
compositions
soap
sodium
detergent
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US591394A
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Melvin E Kamen
Isidore Ugelow
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Revlon Inc
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Revlon Inc
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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D9/00Compositions of detergents based essentially on soap
    • C11D9/04Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
    • C11D9/22Organic compounds, e.g. vitamins
    • C11D9/26Organic compounds, e.g. vitamins containing oxygen
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • C11D10/045Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap based on non-ionic surface-active compounds and soap
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0095Solid transparent soaps or detergents
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/14Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/14Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • C11D1/146Sulfuric acid esters
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

Definitions

  • Solid transparent detergent compositions comprising a sodium soap of a saturated fatty acid, a C -C polyhydric alcohol, and a polyalkoxy ether of an alkyl phenol. Method of making such compositions by dispersing said soap and polyalkoxy ether in said alcohol at elevated temperatures.
  • the present invention relates to solid transparent detergent compositions and to methods of making the same.
  • Detergent compositions of the type prepared according to the present invention have numerous desirable properties. Because of their detergent content, they are useful as cleansing agents with hard Water. Further, the compositions according to the present invention are characterized by an extreme mildness not characteristic of conventional soaps or detergents. The compositions have a very high degree of transparency which permits their manufacture into clear products of considerable esthetic appeal. The compositions of the invention far exceed the definition of transparency discussed in US. Pat. 3,155,624, i.e. sufiicient clarity to permit the reading of bold-face type of about 14 point size through a thickness of a quarterinch of the soap composition. The detergent compositions of the invention can be formed into bars or cakes of higher density and of greater emolliency than conventional transparent soap bars.
  • compositions of the present invention comprise from about 8 to about 22 parts by weight of a sodium soap consisting substantially of sodium soaps of saturated fatty acids having at least 18 carbon atoms.
  • the soaps of practical interest are those of acids having 18-24 carbon atoms, e.g. stearic (C arachidic (C 6), behenic (C and lignoceric (C since these are, presently, the acids commercially available.
  • stearic C arachidic (C 6)
  • behenic C and lignoceric
  • sodium soaps of other long chain fatty acids would be suitable if available in quantity.
  • the use of soaps having a high melting point is recommended.
  • the soap is combined with from about 25 to about 45 parts by weight of a dihydric or trihydric alcohol having 2 or 3 carbon atoms, e.g. ethylene glycol, propylene glycol, and glycerin.
  • a dihydric or trihydric alcohol having 2 or 3 carbon atoms e.g. ethylene glycol, propylene glycol, and glycerin.
  • These polyhydric alcohols can be used alone, admixed with each other or in combination with a minor amount (i.e. up to about an equal amount by 3,562,167 Patented Feb. 9, 1971 weight) of other polyhydric alcohols having up to 12 carbon atoms, e.g. sucrose, lactose, dextrose, sorbitol, and diglycerol.
  • compositions comprise from about 5 to about 30 parts by weight of a polyalkylene glycol ether of an alkyl phenol.
  • Lower polyalkoxy ethers e.g. polyethoxy, polypropoxy, and polybutoxy ethers, of alkyl phenols in which the alkyl group has from 6 to 12 carbon atoms are typical of these commercially available nonionic detergents or wetting agents.
  • Preferred materials are the polyethoxy glycol ethers of alkyl phenols, i.e. alkyl phenoxy polyethoxy ethanols of the formula:
  • G-womomnon wherein R is an alkyl group having from 6 to 12 carbon atoms and x is a number, not necessarily integral since mixtures of compounds may be involved, having an average value from about 7 to 13.
  • Compounds of the latter type are commercially available under the tradenames Igepal (e.g. nonyl phenoxy polyethoxy ethanols, particularly those in which x is from 9 to 11) and Triton (e.g. isooctyl phenoxy polyethoxy ethanols, particularly those in which x is from 7 to 13).
  • the polyhydric alcohol functions as a clarifying solvent for the remaining ingredients and as an emollient.
  • the sodium soap acts primarily as a solidifying agent for the composition.
  • the non-ionic wetting agent plays a detergent role and, further, functions as a coupling agent for the soap and polyhydric alcohol, giving a clearer product than can be obtained in the absence of the detergent. If the compositions are prepared with large amounts of soap, larger amounts of alcohol and detergent, within the limits disclosed, will be needed to solubilize and extend the soap component.
  • foaming agents include soaps of lower fatty acids, such as sodium laurate; alkyl sulfates and alkyl ether sulfates, such as sodium lauryl sulfate and sodium lauryl ether sulfate; sulfobetaines, such as coconut acyl amido sodium sulfonic acid betaines; and alkyl amine oxides such as bis(2-hydroxyethyl) alkylamine oxides or dimethyl alkylamine oxides. These foaming agents can be incorporated in amounts up to about 60 parts by weight with the other ingredients mentioned earlier herein.
  • compositions are conveniently prepared by heating the polyhydric alcohol to a temperature from about 170 F. to about 180 F.
  • the sodium stearate soap is added with stirring until it dissolves to give a clear solution.
  • the solution is then cooled to about 160 F. and the non-ionic detergent component is incorporated into the mixture.
  • the composition is kept above its congealing temperature of about F.- F. until solidification is desired.
  • detergent bars are to be prepared, the compositions need not be milled but are conveniently framed into bars of the desired size and then cooled. Since milling is not required, the manufacture of such bars is particularly simple and economical.
  • glycerin is a preferred material because it has little tendency to discolor on heating. In any event, slight discoloration of any of the components which may be caused by heating is of no consequence if compositions having other than a water-White color are to be prepared.
  • the sodium fatty acid soaps employed are of a purity of at least about 95 percent to minimize the presence of water in the compositions.
  • EXAMPLE 1 A clear detergent composition was prepared by dissolving 18 parts by weight of sodium stearate in 42 parts of glycerin warmed to about 170 F. After slight cooling, 30 parts of nonyl phenoxy polyethoxy ethanol (Igepal) were dispersed in the mixture with stirring. On further cooling, the mixture formed a clear solid mass.
  • Igepal nonyl phenoxy polyethoxy ethanol
  • composition has cleansing properties, and is also useful as a solid vehicle for perfumes and the like.
  • EXAMPLE 2 A closely similar composition was prepared as in Example 1, but employing a mixture of 38 parts of glycerin with parts of propylene glycol as the polyhydroxy component.
  • EXAMPLE 3 42 parts by weight of glycerin and 10 parts of sorbitol were heated to about 170 F. before addition of 18 parts of sodium stearate. After cooling to 160 F., 30 parts of isooctyl phenoxy polyethoxy ethanol (Triton X-100 or X-l02) were added. The composition was then cooled to solidification.
  • Igepal alkyl phenol polyalkylene glycol ether
  • EXAMPLE 5 9 parts by weight of a 30 percent aqueous solution of sodium lauryl sulfate and 10 parts of sodium laurate (70 percent pure) were added as foaming agents, together with 2 parts of perfume and 0.65 part of a soluble dye, to a detergent composition prepared from 17 parts of sodium stearate, 40 parts of glycerin, 10 parts of sorbitol, and 12 parts of alkyl phenoxy polyethoxy ethanol (Igepal). The composition was framed to form detergent bars.
  • sorbitol In place of sorbitol, dextrose, lactose, sucrose, or diglycerol can be combined with the glycerin as an extender and coupling agent.
  • EXAMPLE 6 10 parts by weight of sodium laurate, 2.4 parts by weight of ethoxylated lauryl alcohol, and 40 parts of sodium lauryl ethoxy ether sulfate (60 percent solids) were combined as foaming agents with a detergent composition prepared by dispersing 12 parts of sodium stearate and 7 parts of alkyl phenoxy ethoxy ethanol (Igepal) in 28.6 parts of glycerin.
  • a detergent composition prepared by dispersing 12 parts of sodium stearate and 7 parts of alkyl phenoxy ethoxy ethanol (Igepal) in 28.6 parts of glycerin.
  • foaming agents such as sulfobetaines and alkyl amine oxides can be used to impart foaming properties to the compositions.
  • a detergent composition of particular usefulness as a solid base or carrier for perfume was prepared by combining 10 parts by weight of sodium sterate, 45 parts of ethylene glycol, and 5 parts by weight of alkyl phenoxy polyethoxy ethanol.
  • a solid transparent detergent composition adaptable to forming into bars or cakes and consisting essentially of about 8 to about 22 parts by weight of a sodium soap of a saturated fatty acid having at least 18 carbon atoms, about 25 to about 45 parts by weight of a polyhydric alcohol having 2 or 3 carbon atoms, and about 5 to about 30 parts by weight of a poly(ethoxy) ether of an alkyl phenol in which the alkyl group has from 6 to 12 carbon atoms and the number of ethoxy groups has an average value of from about 7 to 13.
  • a detergent composition as in claim 1 wherein said polyhydric alcohol is propylene glycol.
  • a detergent composition as in claim 1 which additionally contains up to about 60 parts by weight of a foaming agent selected from the group consisting of alkyl sulfates and alkyl ether sulfates.

Abstract

SOLID TRANSPARENT DETERGENT COMPOSITIONS COMPRISING A SODIUM SOAP OF A SATURATED FATTY ACID, A C2-C2 POLYHYDRIC ALCOHOL, AND A POLYALKOXY ETHER OF AN ALKYL PHENOL. METHOD OF MAKING SUCH COMPOSITIONS BY DISPERSING SAID SOAP AND POLYALKOXY ETHER IN SAID ALCOHOL AT ELEVATED TEMPERATURES.

Description

United States Patent US. Cl. 252121 Claims ABSTRACT OF THE DISCLOSURE Solid transparent detergent compositions comprising a sodium soap of a saturated fatty acid, a C -C polyhydric alcohol, and a polyalkoxy ether of an alkyl phenol. Method of making such compositions by dispersing said soap and polyalkoxy ether in said alcohol at elevated temperatures.
The present invention relates to solid transparent detergent compositions and to methods of making the same.
The manufacture of transparent soaps is known in the art, and is typified by the teachings of U.S. Pat. 3,155,624 and the prior art discussed therein. However, transparent compositions containing detergent and of a solidity comparable with that of soap and sufficient to permit processing into cleansing bars or cakes by conventional soapmaking techniques have not heretofore been disclosed.
Detergent compositions of the type prepared according to the present invention have numerous desirable properties. Because of their detergent content, they are useful as cleansing agents with hard Water. Further, the compositions according to the present invention are characterized by an extreme mildness not characteristic of conventional soaps or detergents. The compositions have a very high degree of transparency which permits their manufacture into clear products of considerable esthetic appeal. The compositions of the invention far exceed the definition of transparency discussed in US. Pat. 3,155,624, i.e. sufiicient clarity to permit the reading of bold-face type of about 14 point size through a thickness of a quarterinch of the soap composition. The detergent compositions of the invention can be formed into bars or cakes of higher density and of greater emolliency than conventional transparent soap bars. Because of the low content of volatiles in the compositions (generally less than 5-15 percent of water), bars formed therefrom show no shrinkage and negligible weight loss on storage. In contrast, con. ventional transparent soaps have a high content of water, alcohol, and other volatiles and shaped products formed therefrom may change considerably in size and weight with time. I
The compositions of the present invention comprise from about 8 to about 22 parts by weight of a sodium soap consisting substantially of sodium soaps of saturated fatty acids having at least 18 carbon atoms. The soaps of practical interest are those of acids having 18-24 carbon atoms, e.g. stearic (C arachidic (C 6), behenic (C and lignoceric (C since these are, presently, the acids commercially available. However, sodium soaps of other long chain fatty acids would be suitable if available in quantity. In those compositions containing relatively little soap within the limits given, the use of soaps having a high melting point is recommended.
The soap is combined with from about 25 to about 45 parts by weight of a dihydric or trihydric alcohol having 2 or 3 carbon atoms, e.g. ethylene glycol, propylene glycol, and glycerin. These polyhydric alcohols can be used alone, admixed with each other or in combination with a minor amount (i.e. up to about an equal amount by 3,562,167 Patented Feb. 9, 1971 weight) of other polyhydric alcohols having up to 12 carbon atoms, e.g. sucrose, lactose, dextrose, sorbitol, and diglycerol.
Finally, the compositions comprise from about 5 to about 30 parts by weight of a polyalkylene glycol ether of an alkyl phenol. Lower polyalkoxy ethers, e.g. polyethoxy, polypropoxy, and polybutoxy ethers, of alkyl phenols in which the alkyl group has from 6 to 12 carbon atoms are typical of these commercially available nonionic detergents or wetting agents. Preferred materials are the polyethoxy glycol ethers of alkyl phenols, i.e. alkyl phenoxy polyethoxy ethanols of the formula:
G-womomnon wherein R is an alkyl group having from 6 to 12 carbon atoms and x is a number, not necessarily integral since mixtures of compounds may be involved, having an average value from about 7 to 13. Compounds of the latter type are commercially available under the tradenames Igepal (e.g. nonyl phenoxy polyethoxy ethanols, particularly those in which x is from 9 to 11) and Triton (e.g. isooctyl phenoxy polyethoxy ethanols, particularly those in which x is from 7 to 13).
In the compositions of the present invention, the polyhydric alcohol functions as a clarifying solvent for the remaining ingredients and as an emollient. The sodium soap acts primarily as a solidifying agent for the composition. The non-ionic wetting agent plays a detergent role and, further, functions as a coupling agent for the soap and polyhydric alcohol, giving a clearer product than can be obtained in the absence of the detergent. If the compositions are prepared with large amounts of soap, larger amounts of alcohol and detergent, within the limits disclosed, will be needed to solubilize and extend the soap component.
Additional ingredients such as perfumes, coloring agents, germicides, foaming and lathering agents, and the like can optionally be incorporated into the detergent compositions. Particularly useful commercially available foaming agents include soaps of lower fatty acids, such as sodium laurate; alkyl sulfates and alkyl ether sulfates, such as sodium lauryl sulfate and sodium lauryl ether sulfate; sulfobetaines, such as coconut acyl amido sodium sulfonic acid betaines; and alkyl amine oxides such as bis(2-hydroxyethyl) alkylamine oxides or dimethyl alkylamine oxides. These foaming agents can be incorporated in amounts up to about 60 parts by weight with the other ingredients mentioned earlier herein.
The compositions are conveniently prepared by heating the polyhydric alcohol to a temperature from about 170 F. to about 180 F. The sodium stearate soap is added with stirring until it dissolves to give a clear solution. The solution is then cooled to about 160 F. and the non-ionic detergent component is incorporated into the mixture. The composition is kept above its congealing temperature of about F.- F. until solidification is desired. When detergent bars are to be prepared, the compositions need not be milled but are conveniently framed into bars of the desired size and then cooled. Since milling is not required, the manufacture of such bars is particularly simple and economical.
While there is no criticality in the order in which the ingredients are combined, solution of the stearate soap at a feasible rate requires heating. The preferred process described just above minimizes exposure of the detergent, which is usually the most heat-sensitive component, to
temperatures which might tend to yellow or discolor thecompositions. However, if a heat-resistant detergent is employed, the soap and detergent can be combined prior to addition to the polyhydric alcohol. Of the alcohols,
glycerin is a preferred material because it has little tendency to discolor on heating. In any event, slight discoloration of any of the components which may be caused by heating is of no consequence if compositions having other than a water-White color are to be prepared.
A better understanding of the present invention and of its many advantages will be had by referring to the following specific examples given by way of illustration. In the following examples, the sodium fatty acid soaps employed are of a purity of at least about 95 percent to minimize the presence of water in the compositions.
EXAMPLE 1 A clear detergent composition was prepared by dissolving 18 parts by weight of sodium stearate in 42 parts of glycerin warmed to about 170 F. After slight cooling, 30 parts of nonyl phenoxy polyethoxy ethanol (Igepal) were dispersed in the mixture with stirring. On further cooling, the mixture formed a clear solid mass.
The composition has cleansing properties, and is also useful as a solid vehicle for perfumes and the like.
EXAMPLE 2 A closely similar composition was prepared as in Example 1, but employing a mixture of 38 parts of glycerin with parts of propylene glycol as the polyhydroxy component.
EXAMPLE 3 42 parts by weight of glycerin and 10 parts of sorbitol were heated to about 170 F. before addition of 18 parts of sodium stearate. After cooling to 160 F., 30 parts of isooctyl phenoxy polyethoxy ethanol (Triton X-100 or X-l02) were added. The composition was then cooled to solidification.
EXAMPLE 4 parts by weight of the sodium salt of a fatty acid fraction containing 90 percent of C C fatty acids was dispersed in 40 parts of glycerine together with 30 parts of alkyl phenol polyalkylene glycol ether (Igepal), as in the earlier examples.
EXAMPLE 5 9 parts by weight of a 30 percent aqueous solution of sodium lauryl sulfate and 10 parts of sodium laurate (70 percent pure) were added as foaming agents, together with 2 parts of perfume and 0.65 part of a soluble dye, to a detergent composition prepared from 17 parts of sodium stearate, 40 parts of glycerin, 10 parts of sorbitol, and 12 parts of alkyl phenoxy polyethoxy ethanol (Igepal). The composition was framed to form detergent bars.
In place of sorbitol, dextrose, lactose, sucrose, or diglycerol can be combined with the glycerin as an extender and coupling agent.
EXAMPLE 6 10 parts by weight of sodium laurate, 2.4 parts by weight of ethoxylated lauryl alcohol, and 40 parts of sodium lauryl ethoxy ether sulfate (60 percent solids) were combined as foaming agents with a detergent composition prepared by dispersing 12 parts of sodium stearate and 7 parts of alkyl phenoxy ethoxy ethanol (Igepal) in 28.6 parts of glycerin.
Other commercially available foaming agents such as sulfobetaines and alkyl amine oxides can be used to impart foaming properties to the compositions.
4 EXAMPLE 7 A detergent composition of particular usefulness as a solid base or carrier for perfume was prepared by combining 10 parts by weight of sodium sterate, 45 parts of ethylene glycol, and 5 parts by weight of alkyl phenoxy polyethoxy ethanol.
What is claimed is:
1. A solid transparent detergent composition adaptable to forming into bars or cakes and consisting essentially of about 8 to about 22 parts by weight of a sodium soap of a saturated fatty acid having at least 18 carbon atoms, about 25 to about 45 parts by weight of a polyhydric alcohol having 2 or 3 carbon atoms, and about 5 to about 30 parts by weight of a poly(ethoxy) ether of an alkyl phenol in which the alkyl group has from 6 to 12 carbon atoms and the number of ethoxy groups has an average value of from about 7 to 13.
2. A detergent composition as in claim 1 wherein said fatty acid has from 18 to 24 carbon atoms.
3. A detergent composition as in claim 1 wherein said sodium soap is sodium stearate.
4. A detergent composition as in claim 1 wherein said polyhydric alcohol is propylene glycol.
5. A detergent composition as in claim 1 wherein said polyhydric alcohol is glycerin.
6. A detergent composition as in claim 1 wherein said polyhydric alcohol having 2 or 3 carbon atoms is admixed with up to about an equal amount by weight of a polyhydric alcohol selected from the group consisting of sucrose, lactose, dextrose, sorbitol, and diglycerol.
7. A detergent composition as in claim 1 which additionally contains up to about 60 parts by weight of a foaming agent selected from the group consisting of alkyl sulfates and alkyl ether sulfates.
8. The method of making a solid transparent detergent composition as in claim 1 which comprises dispersing said sodium soap and said poly(ethoxy) ether of an alkylphenol in said polyhydric alcohol at a temperature above the congealing temperature of about F.- F., and up to about 180 F., and then cooling the composition below its solidfication point.
9. The method as in claim 8 wherein sodium stearate and nonyl phenol polyethoxy ethanol are dispersed in glycerin.
10. The method as in claim 8 wherein said sodium soap is first dissolved in said polyhydric alcohol at about F. F., the solution is then cooled to about 160 F. and said polyethoxy ether of an alkyl phenol is added and dispersed therein, and the composition is then cooled below its solidification point.
References Cited UNITED STATES PATENTS OTHER REFERENCES Cracking of Toilet Soaps in Soap & Chemical Specialties, July 1965, pages 147l49.
LEON D. ROSDOL, Primary Examiner D. L. ALBRECHT, Assistant Examiner US. Cl. X.R.
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Cited By (32)

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US3903008A (en) * 1972-05-01 1975-09-02 Lanvin Charles Of The Ritz Inc Cleansing bar
US3975313A (en) * 1974-06-19 1976-08-17 Shelmire Jr Jesse Bedford Solid amphoteric skin cleanser
DE2716442A1 (en) * 1976-04-22 1977-11-03 Colgate Palmolive Co DETERGENT MIXTURE
FR2348967A1 (en) * 1976-04-22 1977-11-18 Colgate Palmolive Co SOLID DETERGENT COMPOSITION FOR LOCAL CLEANING
US4083796A (en) * 1974-08-06 1978-04-11 Armour-Dial, Inc. Dye system for soap and synthetic detergent bars
US4165293A (en) * 1977-05-16 1979-08-21 Amway Corporation Solid transparent cleanser
US4206069A (en) * 1976-04-22 1980-06-03 Colgate-Palmolive Company Transparent detergent pellets
US4256600A (en) * 1978-03-13 1981-03-17 The Greyhound Corp. Translucent soap bar containing citronellyl esters as lime soap dispersants
US4273684A (en) * 1979-05-03 1981-06-16 Ajinomoto Co., Inc. Transparent detergent bar
US4290904A (en) * 1980-12-01 1981-09-22 Neutrogena Corporation Transparent soap
US4297230A (en) * 1979-02-06 1981-10-27 The Procter & Gamble Company Non-crystallizing transparent soap bars
US4396521A (en) * 1976-04-22 1983-08-02 Giuseppe Borrello Solid detergent spotter
FR2532655A1 (en) * 1982-09-02 1984-03-09 Colgate Palmolive Co PROCESS FOR PRODUCING ANTIBACTERIAL TRANSLUCENT SOAP
US4493786A (en) * 1982-09-02 1985-01-15 Colgate-Palmolive Company Translucent soaps and processes for manufacture thereof
WO1988006617A1 (en) 1987-02-26 1988-09-07 Finetex, Inc. Transparent combination soap-synthetic detergent bar
EP0335640A2 (en) * 1988-03-31 1989-10-04 Unilever Plc Transparent soap bars
US4980078A (en) * 1988-03-24 1990-12-25 L'oreal Transparent soap composition based on soaps of tallow fatty acids and water and on at least one 1,2-alkanediol
US4985170A (en) * 1987-10-09 1991-01-15 The Procter & Gamble Company In beta-phase bar form containing soap, high HLB nonionic surfactant, and water-soluble polymer
US5002685A (en) * 1988-07-07 1991-03-26 Lever Brothers Company, Division Of Conopco, Inc. Translucent detergent bar having a reduced soap content
US5258136A (en) * 1992-03-04 1993-11-02 Application Chemicals, Inc. Alkoxylated compounds and their use in cosmetic stick formulations
FR2694569A1 (en) * 1992-08-10 1994-02-11 Icc France Solid transparent hygiene article, e.g. soap or shampoo - contg. carrier, foaming surfactant, multi-component mixt. conferring transparency, and component causing solidification
US5310495A (en) * 1986-11-04 1994-05-10 Lever Brothers Company, Division Of Conopco, Inc. Transparent soap bar
US5443821A (en) * 1992-03-04 1995-08-22 Application Chemicals, Inc. Alkoxylated compounds and their use in cosmetic stick formulations
WO1996004361A1 (en) * 1994-08-03 1996-02-15 The Procter & Gamble Company Process for making a transparent personal cleansing bar
WO1996004360A1 (en) * 1994-08-03 1996-02-15 The Procter & Gamble Company Transparent personal cleansing bar
EP0709453A2 (en) * 1994-10-13 1996-05-01 Vioryl Chemical And Agricultural Industry Research S.A. Method for the production of transparent soap
US5571287A (en) * 1993-01-11 1996-11-05 Colgate-Palmolive Company Soap composition containing sodium pyrophosphate
US5993371A (en) * 1996-01-22 1999-11-30 Henkel Corporation Transparent soap bars containing alkyl polyglycosides
US6297205B1 (en) 1999-08-30 2001-10-02 Amway Corporation Monohydric alcohol-free transparent moisturizing bar soap

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US3793214A (en) * 1971-10-22 1974-02-19 Avon Prod Inc Transparent soap composition
US3926828A (en) * 1971-10-22 1975-12-16 Avon Prod Inc Method of making transparent soap bars
US3903008A (en) * 1972-05-01 1975-09-02 Lanvin Charles Of The Ritz Inc Cleansing bar
JPS49103909A (en) * 1973-02-01 1974-10-02
JPS50110404A (en) * 1974-02-12 1975-08-30
JPS5230286B2 (en) * 1974-02-12 1977-08-06
US3975313A (en) * 1974-06-19 1976-08-17 Shelmire Jr Jesse Bedford Solid amphoteric skin cleanser
US4083796A (en) * 1974-08-06 1978-04-11 Armour-Dial, Inc. Dye system for soap and synthetic detergent bars
US4396521A (en) * 1976-04-22 1983-08-02 Giuseppe Borrello Solid detergent spotter
FR2360663A1 (en) * 1976-04-22 1978-03-03 Colgate Palmolive Co DETERGENT COMPOSITION
DK154347B (en) * 1976-04-22 1988-11-07 Colgate Palmolive Co DETERGENT AND PROCEDURE FOR PREPARING THEREOF
US4206069A (en) * 1976-04-22 1980-06-03 Colgate-Palmolive Company Transparent detergent pellets
FR2348967A1 (en) * 1976-04-22 1977-11-18 Colgate Palmolive Co SOLID DETERGENT COMPOSITION FOR LOCAL CLEANING
DE2716442A1 (en) * 1976-04-22 1977-11-03 Colgate Palmolive Co DETERGENT MIXTURE
DK155749B (en) * 1976-04-22 1989-05-08 Colgate Palmolive Co TRANSPARENT, WATER SOLUBLE, NON-COMPLIANT AND IN ESSENTIAL NON-HYGROSCOPIC DETERGENT BOWLS
US4165293A (en) * 1977-05-16 1979-08-21 Amway Corporation Solid transparent cleanser
US4256600A (en) * 1978-03-13 1981-03-17 The Greyhound Corp. Translucent soap bar containing citronellyl esters as lime soap dispersants
US4297230A (en) * 1979-02-06 1981-10-27 The Procter & Gamble Company Non-crystallizing transparent soap bars
US4273684A (en) * 1979-05-03 1981-06-16 Ajinomoto Co., Inc. Transparent detergent bar
EP0053222A1 (en) * 1980-12-01 1982-06-09 Neutrogena Corporation Transparent soap
US4290904A (en) * 1980-12-01 1981-09-22 Neutrogena Corporation Transparent soap
US4493786A (en) * 1982-09-02 1985-01-15 Colgate-Palmolive Company Translucent soaps and processes for manufacture thereof
FR2532655A1 (en) * 1982-09-02 1984-03-09 Colgate Palmolive Co PROCESS FOR PRODUCING ANTIBACTERIAL TRANSLUCENT SOAP
US5310495A (en) * 1986-11-04 1994-05-10 Lever Brothers Company, Division Of Conopco, Inc. Transparent soap bar
US4851147A (en) * 1987-02-26 1989-07-25 Finetex, Inc. Transparent combination soap-synthetic detergent bar
WO1988006617A1 (en) 1987-02-26 1988-09-07 Finetex, Inc. Transparent combination soap-synthetic detergent bar
US4985170A (en) * 1987-10-09 1991-01-15 The Procter & Gamble Company In beta-phase bar form containing soap, high HLB nonionic surfactant, and water-soluble polymer
US4980078A (en) * 1988-03-24 1990-12-25 L'oreal Transparent soap composition based on soaps of tallow fatty acids and water and on at least one 1,2-alkanediol
EP0335640A2 (en) * 1988-03-31 1989-10-04 Unilever Plc Transparent soap bars
EP0335640A3 (en) * 1988-03-31 1990-10-10 Unilever Plc Transparent soap bars
US5041234A (en) * 1988-03-31 1991-08-20 Lever Brothers Company, Division Of Conopco, Inc. Transparent soap bars which may contain short chain monohydric alcohols, and a method of making the same
US5002685A (en) * 1988-07-07 1991-03-26 Lever Brothers Company, Division Of Conopco, Inc. Translucent detergent bar having a reduced soap content
US5443821A (en) * 1992-03-04 1995-08-22 Application Chemicals, Inc. Alkoxylated compounds and their use in cosmetic stick formulations
US5258136A (en) * 1992-03-04 1993-11-02 Application Chemicals, Inc. Alkoxylated compounds and their use in cosmetic stick formulations
FR2694569A1 (en) * 1992-08-10 1994-02-11 Icc France Solid transparent hygiene article, e.g. soap or shampoo - contg. carrier, foaming surfactant, multi-component mixt. conferring transparency, and component causing solidification
US5571287A (en) * 1993-01-11 1996-11-05 Colgate-Palmolive Company Soap composition containing sodium pyrophosphate
WO1996004361A1 (en) * 1994-08-03 1996-02-15 The Procter & Gamble Company Process for making a transparent personal cleansing bar
WO1996004360A1 (en) * 1994-08-03 1996-02-15 The Procter & Gamble Company Transparent personal cleansing bar
EP0709453A2 (en) * 1994-10-13 1996-05-01 Vioryl Chemical And Agricultural Industry Research S.A. Method for the production of transparent soap
EP0709453A3 (en) * 1994-10-13 1998-11-25 Vioryl Chemical And Agricultural Industry Research S.A. Method for the production of transparent soap
US5993371A (en) * 1996-01-22 1999-11-30 Henkel Corporation Transparent soap bars containing alkyl polyglycosides
US6297205B1 (en) 1999-08-30 2001-10-02 Amway Corporation Monohydric alcohol-free transparent moisturizing bar soap
US6462002B2 (en) 1999-08-30 2002-10-08 Access Business Group International Llc Monohydric alcohol-free transparent moisturizing bar soap with plastic packaging mold

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