THE PRIOR ART

It is generally known that the protective measures for healthy skin include, among other things, that the skin surface maintains a certain hygroscopicity. When the substances, on which this hygroscopicity and its continuous restoration are based, are removed from the skin by environmental influences, such as repeated washing with substances having highly wetting and extracting effects, chemical influences and the strong effects of weathering, the epidermis is subjected to changes which can greatly reduce the protective action of the skin against injurious environmental influences.

Therefore, the task arose of providing cosmetic agents, particularly agents for the care, protection and cleaning of the skin, by means of which the ability of the skin to function is fully maintained or enhanced despite the injurious environmental influences, and by means of which the restoration of the epidermis is effectively assisted when damage to the skin has occurred.

The products hitherto used as agents for keeping the skin moist were, without exception, ionic compounds such as acids and, primarily salts, which, although they produced reliable results as skin moisture regulators in many cases, frequently caused difficulties when incorporated in the cosmetic preparations, especially if the bases were sensitive emulsions. In such cases, it was frequently not possible to incorporate fully adequate quantities of skin moisture regulators. Furthermore, in addition to the general task of developing satisfactory agents for keeping the skin moist, a particular interest was attached to developing products which do not cause any difficulties even when they are incorporated in more sensitive cosmetic emulsions.

OBJECTS OF THE INVENTION

It is an object of the present invention to provide a skin-care, skin-protection, and skin-cleaning agent composition containing at least one hydroxyalkane carboxylic acid amide as a skin moisturizing agent.

It is another object of the present invention to provide a skin-care and skin-protection agent composition, by means of which the functional capacity of the skin may be maintained or increased in spite of harmful environmental influences, and which effectively supports the restoration of the horny layer, should any damage have been incurred.

These and further objects of the invention will become apparent as the description thereof proceeds.

DESCRIPTION OF THE INVENTION

The present invention relates to skin-care, skin-protection and skin-cleaning agent compositions containing at least one hydroxyalkane carboxylic acid amide as a skin moisturizing agent.

Accordingly, the present invention involves cosmetic agents, particularly agents for the care, protection and cleaning of the skin, comprising conventional constituents, such as surfactants, emulsifiers, fatty substances, vegetable extracts, solvents, perfumes, thickening agents, and preservatives, and from 1 to 20 percent by weight, preferably 3 to 10 percent by weight, relative to the total weight of the cosmetic agent, of at least one hydroxyalkane carboxylic acid amide of the formula ##STR1## wherein R₁ and R₂ are independently of each other a member selected from the group consisting of hydrogen and an alkyl radical having 1 to 4 carbon atoms, R₃ is a member selected from the group consisting of the direct bond, a straight-chain alkylene radical having 1 to 3 carbon atoms and a straight-chain alkylene radical having 1 to 3 carbon atoms substituted by one or more alkyl and/or hydroxyalkyl groups and R₄ and R₅ independently of one another are a member selected from the group consisting of hydrogen, an alkyl radical having 1 to 4 carbon atoms and an hydroxyalkyl radical having 2 to 6 carbon atoms and 1 to 5 hydroxyl groups.

R₁ and R₂ can each very suitably be hydrogen or methyl. The straight-chain alkylene radical R₃ can, for example, be substituted by 1 to 4 groups selected from alkyl of 1 to 4, preferably 1, carbon atoms, hydroxyalkyl of 1 to 4, preferably 1, carbon atoms or any combination of said alkyl and hydroxyalkyl groups.

More particularly, the present invention provides a cosmetic agent composition for the care and protection of the skin of warm-blooded animals consisting essentially of from 1% to 20% by weight based upon the total weight of at least one hydroxyalkane carboxylic acid amide of the formula ##STR2## wherein R₁ and R₂ are independently of each other a member selected from the group consisting of hydrogen and an alkyl radical having 1 to 4 carbon atoms, R₃ is a member selected from the group consisting of the direct bond, a straight-chain alkylene radical having 1 to 3 carbon atoms and a straight-chain alkylene radical having 1 to 3 carbon atoms substituted by one or more alkyl and/or hydroxyalkyl groups and R₄ and R₅ independently of one another are a member selected from the group consisting of hydrogen, an alkyl radical having 1 to 4 carbon atoms and an hydroxyalkyl radical having 2 to 6 carbon atoms and 1 to 5 hydroxyl groups; and the remainder conventional cosmetic excipients.

In addition the present invention provides a process for the care and protection of the skin of warm-blooded animals comprising topically applying to the skin a safe but effective amount of the agent composition mentioned above.

The hydroxyalkyl carboxamides which are used in the agent compositions of the invention are extremely suitable for maintaining or restoring the water retention of the skin and thus for keeping the skin soft, flexible and fully capable of performing its function.

The compounds of the invention can be produced by generally known methods. Thus, for example, they can be obtained by aminolysis of the alkyl esters or lactones of the corresponding hydroxyalkanoic acids in a solvent-free method or in solvents such as alkanols, dioxane or tetrahydrofuran. Furthermore, the hydroxyalkyl carboxamides can be obtained from the hydroxyalkanoic acids and the corresponding amines by heating these reactants to higher temperatures, with or without solvents. Solvents for the azeotropic separation of water, may be, for example, toluene, xylene, chlorobenzene or ligroin.

Examples of hydroxyalkyl carboxamides to be used in accordance with the invention are glycolic acid amide, lactic acid amide, α-hydroxybutyric acid amide, β-hydroxybutyric acid amide, γ-hydroxybutyric acid amide, α-hydroxyisobutyric acid amide, β-hydroxyisobutyric acid amide, α-hydroxyvaleric acid amide, γ-hydroxyvaleric acid amide, and α,α-bis-hydroxymethylpropionic acid amide.

Further examples are the following N-substituted and N,N-disubstituted derivatives of glycolic acid amide: the N-methyl-, N-ethyl-, N-propyl-, N,N-dimethyl-, N,N-diethyl-, N-butyl-, N-(2-hydroxyethyl)-, N-(2-hydroxypropyl)-, N-(3-hydroxy-propyl)-, N-(2-hydroxybutyl)-, N-(1-hydroxy-2-methyl-2-propyl)-, N-(2,3-dihydroxypropyl)-, N-(1,3-dihydroxy-2-propyl)-, N-(1,3-dihydroxy-2-methyl-2-propyl)-, N-(1,3-dihydroxy-2-ethyl-2-propyl)-, N-(trishydroxymethyl-methyl)-, N-(2-hydroxyethyl)-N-methyl-, N-(2-hydroxypropyl)-N-methyl-, N-(2,3-dihydroxypropyl)-N-ethyl-, N-(2,3,4,5,6-pentahydroxy-hexyl)-, N-(1,3,4,5,6-pentahydroxy-2-hexyl)-, N,N-bis-(2-hydroxyethyl)-, N,N-bis-(2-hydroxypropyl)-, and N-(2-hydroxyethyl)-N-(2-hydroxypropyl)-derivatives. Other useful carboxamides of the invention are the above analogous N- substituted and N,N-disubstituted derivatives of each of the following hydroxyalkyl carboxamides: lactic acid amide, α-hydroxybutyramide, β-hydroxybutyramide, γ-hydroxybutyramide, α-hydroxyisobutyramide, β-hydroxyisobutyramide, α-hydroxyvaleramide, α-hydroxy-valeramide, and α-α-bis-hydroxymethyl-propionamide, i.e., N-methyl-lactic acid amide, N-ethyl-lactic acid amide, N-propyl-lactic acid amide, etc.

Very advantageous results have been obtained with those hydroxyalkyl carboxylic acid amides of the invention wherein R₄ is hydroxyalkyl and R₅ is hydrogen or both R₄ and R₅ are hydroxyalkyl. It has also been found that good results can be obtained by having one or more hydroxyalkyl groups on the R₃ alkylene radical. The hydroxymethyl group is an example of such an especially suitable hydroxyalkyl substituent.

The hydroxyalkyl carboxamides of the invention are colorless to bright yellow colored, crystalline or highly viscous, fully stable products, which have very satisfactory physiological compatibility and, acting as neutral, non-ionic compounds, are distinguished by the fact that they can be incorporated in cosmetic emulsion bases in a particularly satisfactory manner.

It was found that the functional capacity of the skin may be maintained or restored even to a higher degree than before if it is treated with agents for the care and protection of the skin, which besides the customary constituents include from 1% to 20% by weight, preferably 3% to 10% by weight, based on the total composition of the hydroxyalkane carboxylic acid amides in accordance with the invention.

Among the compositions for the care and protection of the skin having special skin-caring properties due to the addition of the hydroxyalkane carboxylic acid amides used in accordance with the invention are emulsions of the oil-in-water type or water-in-oil type.

Examples of agents for the care, protection and cleaning of the skin, to which special skin-care properties are imparted by the addition of the hydroxyalkane carboxylic acid amides of the invention are the conventional day creams, baby creams, night and nutrient creams, cleansing creams, skin protection creams, glycerol creams, creams having special additives of animal and vegetable origin, creams and emulsions for protection against the sun and sun tanning creams, soaps, bath oils, foam baths, shower baths, face lotions, and after-shave lotions. They can be incorporated in the agents for the care, protection and cleansing of the skin in a known manner simply by stirring-in or dissolving. In addition to the amides of hydroxyalkane carboxylic acids used in accordance with the invention, the cosmetic preparations can also contain conventional quantities of the constituents usually contained therein, such as emulsifiers, fatty substances, vegetable extracts, thickeners, preservatives, surfactants, perfumes and solvents. Water and lower alcohols, such as methanol, ethanol and isopropanol, serve as very useful constitutents of the cosmetic preparations of the invention. Lower alcohols of 1-3 carbon atoms are very suitable. The pH value of the agents for the care and protection of the skin may be in the range of acid to neutral (approximately pH 5-7.0) and, advantageously, is adjusted to a weakly acid value of approximately pH 6. The skin cleansing agents based on soap should be adjusted so as to have as weak an alkaline pH value as possible.

The following examples are intended to illustrate the subject of the invention without, however, limiting it to these examples.

EXAMPLES

The production of some of the amides of hydroxyalkane carboxylic acids of the invention is described below.

EXAMPLE 1

Product A2: N-propyl-lactic acid amide [J.Org.Chem. 15,317(1950)]

A mixture of 35.4 gm (0.3 mole) of ethyl lactate and 19.4 gm (0.33 mole) of propylamine were stirred together at 60° C. for 16 hours and subsequently distilled under reduced pressure. 30 gm (76% of theory) of N-propyl-lactic acid amide of boiling point 152° C./9 torr and of refractive index (n_D ²⁰) 1.4563 were obtained.

Product A3: N-(2-hydroxyethyl)-lactic acid amide

A mixture of 70.8 gm (0.6 mole) of ethyl lactate and 36.6 gm (0.6 mole) of ethanolamine were stirred together at 60° C. for 16 hours, and the ethanol formed was subsequently distilled off under reduced pressure. 71 gm (89% of theory) of light yellow, viscous N-(2-hydroxyethyl)-lactic acid amide of refractive index (n_D ²⁰) 1.4850 were obtained.

Product B1: N-(2-hydroxyethyl)-γ-hydroxybutyramide

A solution of 24.4 gm (0.4 mole) of ethanolamine in 30 ml of methanol were slowly added dropwise with stirring to a solution of 34.4 gm (0.4 mole) of γ - butyrolactone in 50 ml of methanol. The temperature rose to 50° C. The mixture was subsequently heated for 3 hours at boiling and the methanol was distilled off under reduced pressure. A quantitative yield of N-(2-hydroxyethyl)-γ-hydroxybutyramide was obtained in the form of a colorless viscous liquid. The compound became crystalline after standing for a long period of time and melts at 54° to 56° C.

The following amides of hydroxyalkane carboxylic acids were produced in accordance with the methods described in the above Examples. Reaction parameters, properties and some literature references are presented in TABLE 1 below for the amides. Products A2, A3 and B1 are also included in the table.

                                  TABLE 1__________________________________________________________________________     Reaction       Properties     Remarks,     Conditions     m.p. or b.p.                            Recrystal-                                   Litera-     Temp.          Time      (° C/torr);                            lized  tureProduct   ° C          Hours               Solvent                    nD 20                            from   References__________________________________________________________________________Al: Lacticacid amide     --   --   --   70      Ethyl- Beilst.                            acetate                                   3 II 208A2: N-propyllactic acid     60   16   --   152/9   --     J.O.C.amide                    1.4563         15,317                                   (1950)A3: N-(2-hy-droxyethyl)                             Light yel-lactic acid     60   16   --   1.4850  --     low, vis-amide                                   cous oilA4: N-(2-hy-hydroxypropyl)                          Light yel-lactic acid     60   16   --   1.4773  --     low, vis-amide                                   cous oilA5: N-(2-hy-                            Light yel-droxy-isobut-     80   8    --   1.4741  --     low, vis-yl) lactic                              cous oilacid amide                              Product ex-                                   tracted with                                   not etherA6: N-(1,3-di-     80   8    --   79-80   2-pro-hydroxy-2-me-                    panol/thyl-2-propyl)                   petro-lactic acid                      leum etheramideA7: N-(tris-hydroxy-met-     80   6    --   1.5057  --     Light yel-hyl-methyl)                             low, vis-lactic acid                             cous oilamideA8: N,N-bis-(2-hydroxy-     60   16   --   1.4818  --     Colorlessethyl) lactic                           resinacid amideA9: N,N-bis-(2-hydroxy-     60   16   --   1.5011propyl)lacticacid amideB1: N-(2-hydroxyethyl-     65   3    Methanol                    54-56   --     Precipi-γ-hy-                             tated asdroxy-butyra-                           a color-amide                                   less resinB2: N-(2-hydroxypro-pyl)-γ-hydroxy-  65   3    Methanol                    1.4889  --     Colorlessbutyramide                              resinB3: N-(2-hydroxy-iso-     78   6    Ethanol                    1.4870  --     Colorlessbutyl)-γ-     +120 4                        resinhydroxy-butyramideB4: N-(1,3-dihydroxy-2-     78   6    Ethanol                    1.4981  --     Light yel-methyl-2- +120 4                        low, vis-propyl)-γ-                        cous oilhydroxy-butyramideB5: N-(tris-     78   8    Ethanol                    88-90   --     Colorlesshydroxy-                                resinmethyl-met-hyl-γ-hy-droxy-butyr-amideB6: N,N-bis-(2-hydroxy-     78   6    Ethanol                    1.5049  --     Light yel-ethyl-γ-     +120 5                        low, vis-hydroxy-                                cous oilbutyramideB7: N,N-bis-(2-hydroxy-propyl)-γ-     78   6    Ethanol                    1.4891  --     Light yel-hydroxy-  +120 6                        low, vis-butyramide                              cous oilC1: N-(2-hy-droxyethyl)-     60   16        138-140/α-hy-     +70  9    --   0.01    --     Colorless,droxy-iso-               1.4778         viscousbutyramide                              oilC2: N-(2-hy-droxypropyl)-     66   16        136/0.01α-hydroxy     +70  9         64-65   --     ColorlessisobutyramideC3: N-(2-hy-droxy-iso-butyl)-α-     60   16   --   88-90   ether/butyl)-α-     60   16   --   88-90   ether/hydroxy-iso-                     chloroform                                   ColorlessbutyramideD1: Glycolic     80-  4    H2 O                    115     ethanol                                   Beilsteinacid amide     100                           3,240D2: N-(2-hydroxy-  90-ethyl)glycolic     100  16   --   72      methanol                                   colorless,acid                                    US Patentamide                                   2 347 494D3: N-(2-hy-droxy-pro-     90-pyl)-glycolic     100  16   --   57      ethanol                                   colorlessacid amideD4: N-(tris-hydroxy-  90-methyl-met-     100  16   --   --      --     colorlesshyl)-glycolic                           wax-likeacid amideD5: N,N-bis-(2-hydroxy-     90-                           Light yel-ethyl)-   100  16   --   --      --     low resinglycolic acid                           Belgianamide                                   Patent                                   622 170E1: α,α-bis-hydroxy-  10-20          1-2  methanol                    104-105 Productmethyl-pro-                      washed withpionic acid                      chloroformamideE2: N-(2-hy-droxyethyl)-     60   24   --   1.4732  --     Light yel-α,α-bis-hy-                 low, vis-droxymethyl-                            cous oilpropionicacid amide__________________________________________________________________________

The favorable activity of the compounds to be used in accordance with the invention with respect to hygroscopicity and water retention capacity was determined by means of the test methods described below. These methods involve the determination of the equilibrium moisture which is indicative of the water retention capacity, and the determination of the water retention, rehydration and resilience of impregnated pig epidermis.

EXAMPLE 2

(1) Determination of the equilibrium moisture

The substances (approximately 300 to 500 mg) to be tested were moistened with a defined quantity of water and were exposed for 24 hours at 23° C. to various relative atmospheric humidities (1%, 30%, 47%, 65%, 89% and 100% relative humidity). The quantity of water absorbed or desorbed was determined gravimetrically and recorded graphically. The relative humidity at which water is neither given off nor absorbed can be determined from the resultant curves. This value, designated "equilibrium moisture," is a gauge of the capacity of a substance to retain water. The lower the value, the more desirable the substance is from the standpoint of its water retention capacity. Furthermore, the hygroscopicity of the substance can be read from the slope of the curve.

(2) Measurements on pig epidermis

(a) Obtaining the pig epidermis

The skin bristles are cut off by means of hair clippers (shearing head of 0.1 mm) immediately after the pigs have been killed. The pigs are soaked for approximately 3 to 5 minutes in water heated to 60° C. The epidermis is subsequently peeled off and stored at -20° C. until it is used.

(b) Determining the water retention and the rehydration of impregnated pig epidermis

Punched out pieces of epidermis (1 × 2 cm) were soaked for two hours in a 10% solution of the test substance; excess moisture was removed under standardized conditions by means of a small press; and the pieces were dried for 24 hours, hanging freely between 2 clamps in a 100 ml Erlenmeyer flask at 23° C. and at 30% relative humidity and 50% relative humidity (set by mixtures of sulfuric acid and water). The drying of the impregnated test pieces to X% of the initial weight was compared with the corresponding value of the epidermis which had been soaked only in water (control value). The improvement in the water retention and in the rehydration as compared with the control value is given in Δ% H₂ O in the following Table 2. The deviations in each double test amounted to a maximum of ± 2 absolute units. The test was repeated if greater deviations occurred. The rehydration was determined analogously by drying the pig epidermis, which had been impregnated and from which the excess moisture had been removed, for 24 hours at 30% relative humidity, and by subsequent incubation for 24 hours at 90% relative humidity.

(c) Measurement of elasticity of impregnated pig epidermis

Punched-out pieces of epidermis (1 × 6 cm) were soaked for two hours in a 10% aqueous solution of the substance which was to be tested and excess moisture was removed from these pieces under standardized conditions. The test pieces were incubated for 24 hours, hanging freely between 2 clamps at 75% relative humidity and at 90% relative humidity, and were stretched in a Zwick twist-tensile-testing machine (type: 1402) under a load of 0 to 50 pond(p). The expansion in mm, measured in the Hooke range at a load between 5 to 30 pond(p), was used as a gauge for the elasticity.

The measured values obtained in the previously described tests are presented in the following TABLE 2.

                                  TABLE 2__________________________________________________________________________Measurements made on pig epidermis       Water retention in                   Rehydration in                            mm expansion afterEquilibrium Δ% H2 O after                   Δ%H2 O absorp-                            loading between 5moisture    drying at   tion at 90%                            and 30 p atProduct(% r.h.)       30% r.h.             50% r.h.                   r.h.     90% r.h.                                  75% r.h.__________________________________________________________________________Controlvalue--      0     0     0       0.3-0.5                                  0A174     10    13    31       3.2   0.9A372     11    17    31       3.1   1.3A472     11    18    29       4.1   1.0A572     16    13    23       2.8   0.7A674     14    17    20       2.7   0.7A770     10    12    23       3.6   1.0A869     13    16    24       2.0   0.5A969      9    15    26       2.5   0.7B157      9    14    28       3.6   1.5B258      9    17    28       2.8   0.7B365     11    12    17       4.2   0.8B470      8    13    20       4.1   1.0B565     11    12    22       3.8   0.7B670     11    12    25       3.1   1.0B770     10    17    27       3.6   0.9C170     16    17    26       4.5   0.5E285     13    14    21       2.6   0.7__________________________________________________________________________ "--" not measured

In addition to showing the high hygroscopicity of the compounds of the invention, the above Table also shows their considerable water-retention capacity, and thus their eminent suitability for use as agents for keeping the skin moist in preparations for the care, protection and cleansing of the skin.

Some examples of cosmetic preparations containing substances of the invention, as agents for keeping the skin moist, are given below. The quantities of all ingredients are given in parts by weight.

EXAMPLE 3

______________________________________Slightly greasy day cream                  Parts______________________________________Fatty acid partial glyceride Cutina MD.sup.®  Dehydag                  6.0Stearic acid           8.0Mixture of non-ionic emulsifiers Emulgin C 700.sup.®  Dehydag                  3.02-octyldodecanol       4.0Vegetable oil          3.0Paraffin oil           5.0Triethanolamine        0.41,2-propylene glycol   3.0Product Al             6.0Nipagin M              0.2Perfume oil            1.0Water                  60.4______________________________________

EXAMPLE 4

______________________________________Baby cream             Parts______________________________________Mixture of higher molecular esters,predominantly mixed esters ofpentaerythritol fatty acid esterand citric acid fatty alcohol esterDehymuls E.sup.® Dehydag                  7.0Decyl oleate           10.0Vaseline.sup.®     10.0Lanolin                5.0Boric acid             0.2Talc                   12.0Zinc oxide             8.0Nipagin M              0.2Product A4             8.0Water                  39.6______________________________________

EXAMPLE 5

______________________________________Night cream            Parts______________________________________Colloidally dispersed mixtureof 90 parts of cetyl/stearylalcohol and 10 parts of sodiumlauryl sulfate         10.02-octyldodecanol       12.0Vegetable oil          7.0Lanolin                2.0Glycerol               1.0Product A3             10.0Nipagin M              0.2Perfume oil            1.0Water                  56.8______________________________________

EXAMPLE 6

______________________________________Boro-glycerol cream    Parts______________________________________Colloidally dispersed mixtureof 90 parts of cetyl/stearylalcohol and 10 parts ofsodium lauryl sulfate  12.02-octyldodecanol       8.0Vegetable oil          5.0Boric acid             2.0Glycerol               28.0Nipagin M              0.2Product B1             6.0Water                  38.8______________________________________

EXAMPLE 7

______________________________________Sun protection cream   Parts______________________________________Mixture of higher molecularesters with fatty substancesDehymuls K.sup.® Dehydag                  30.0Decyl oleate           15.0Light protection agent 5.0Nipagin M              0.2Product B2             8.0Water                  41.8______________________________________

EXAMPLE 8

______________________________________Fase Mask              Parts______________________________________Mixture of fatty acid partialglyceride with emulsifiersCutain LE.sup.® Dehydag                  12.0Decyl oleate           4.0Vitamin oil            5.0Kaolin                 2.0Rice starch            3.0Nipagin M              0.2Product A9             10.0Water                  63.8______________________________________

EXAMPLE 9

______________________________________After Shave lotion  PartsOleyl/cetyl alcohol 1.0Ethanol 96%         67.5Methanol            0.2Camphor             0.2Peru balsam         0.1Perfume             0.5Hammamelis extract  10.0Boric acid          0.5Product A8          5.0Product B6          5.0Water               10.0______________________________________

EXAMPLE 10

______________________________________Face lotion         Parts______________________________________Cucumber juice      15.0Citric acid         0.2Ethanol 96%         15.0Product A8          5.0Product B7          5.0Perfume             1.0Water               58.8______________________________________

EXAMPLE 11

______________________________________Foam bath              Parts______________________________________Monoethanolamine lauryl sulfatecontaining approximately 33%active washing substance                  66.0Coconut fatty acid diethanolamide                  3.0Product Cl             10.0Perfume oil            3.0Water                  18.0______________________________________

EXAMPLE 12

______________________________________Cream foam bath      Parts______________________________________Sodium lauryl ether sulfatecontaining approximately 30%active washing substance                78.0Oleic acid diethanolamide                4.0Hexyl laurate        8.0Product A3           5.01,2-propylene glycol 2.0Perfume oil          3.0______________________________________

EXAMPLE 13

Soap containing agents for keeping the skin moist

A mixture of 80% of sodium tallow soap and 20% of sodium coconut soap was used. The soap, in the form of flakes and having a water content of 20%, was mixed with

0.2 parts of 1-hydroxyethane-1,1-diphosphonic acid,

10.0 parts Product Al, and

3.0 parts Perfume oil,

relative to 100 parts by weight of soap, and was deformed in an extrusion press and pressed to form cakes.

EXAMPLE 14

Syndet cake of soap containing agents for keeping the skin moist

The Syndet cake of this example was based on a mixture of olefin sulphonate and sulpho-succinic ester salt. The disodium salt of a sulphosuccinic acid mono-fatty alcohol ester, produced from the C₁₂ -C₁₈ fraction of a coconut fatty alcohol, was used in preparing the mixture. The olefin sulphonate was derived from a mixture of straight-chain α-olefins having 15 to 18 carbon atoms. This olefin mixture was produced by sulphonation of 1 mole of olefin with approximately 1.2 moles of gaseous sulfur trioxide diluted with an inert gas, hydrolysis of the raw product of sulphonation with the calculated quantity of caustic soda at a temperature of approximately 100° C., and bleaching of the sulphonate by means of hypochlorite. The mixture of the two sulphonates contained approximately 5 percent by weight of neutral salts (sodium sulfate and sodium chloride) relative to the anhydrous sulphonate. The Syndet composition contained the following ingredients:

70 parts by weight of a surfactant mixture of 60 percent by weight of the olefin sulphonate and

40 percent by weight of the disodium salt of the sulphosuccinic acid ester

15 parts by weight of stearic fatty acid (iodine number 2)

2 parts by weight of lanolin

5 parts by weight of water

8 parts by weight of Product A4

2 parts by weight of perfume oil.

The Syndet composition was deformed in an extrusion press and pressed to form cakes.

In place of the compounds used in accordance with the invention mentioned in the above examples, others of the products in accordance with the invention may be used with equally good success.

The preceding specific embodiments are illustrative of the practice of the invention. It is to be understood, however, that other expedients known to those skilled in the art, or given herein, may be employed without departing from the spirit of the invention or the scope of the appended claims.