METHOD AND AGENTS FOR PERMANENTLY STYLING HAIR, WITH A BASE CONSISTING OF N,N-DISUBSTITUTED MERCAPTOACETAMIDES, AND METHOD FOR PRODUCING SAID MERCAPTOACETAMIDES

Abstract

1 The invention relates to a method and agents for permanently styling hair, characterised in that they contain a keratin reduction agent in the form of N,N-disubstituted mercaptoacetamide of general formula (I) or salts thereof, R1 and R2 representing a straight-chain or branched alkyl radical, monohydroxyalkyl or polyhydroxyalkyl or carboxyalkyl, each with 1 to 6 carbon atoms. The invention also relates to a method for producing these mercaptoacetamides and to the novel mercaptoacetamide N-ethyl-N-2′-hydroxy-ethylmercaptoacetamide. The inventive agent enables the hair to be styled gently and evenly, at a pH range—4.5 to 9.5—which is gentle on skin and hair, without causing allergic or sensitizing reactions.

Description

[0001] The invention relates to agents and methods for permanent hair shaping containing as the keratin-reducing active ingredient an N,N-disubstituted mercaptoacetamide, to a method for producing such mercaptoacetamides and to the new mercaptoacetamide N-ethyl-N-2′-hydroxyethyl mercaptoacetamide.

[0002] As is known, the conventional technique for achieving permanent hair shaping consists of two processing steps: In the first step, the cystine disulfide bonds of hair keratin are broken by the action of an agent containing a reducing substance (shaping agent). Then, the hair is shaped as desired. In a second step, the cystine disulfide bonds are reformed by means of a fixing agent, namely an agent containing an oxidizing substance.

[0003] As shown by the pioneering work described in German Patents 948 186 and 972 424, the conventional permanent wave reducing agent is thioglycolic acid used, for example, in the form of its ammonium or monoethanolamine salt. Other common reducing substances are inorganic sulfites, 2-mercaptopropionic acid (thiolactic acid), 3-mercaptopropionic acid, certain mercaptocarboxylic esters, cysteine and derivatives of these compounds.

[0004] All these agents, however, have a number of drawbacks. Alkaline preparations based on mercaptocarboxylic acids, in spite of adequate efficacy, cause hair damage manifesting itself, for example, by extensive hair breakage. Frequently, these agents also have an undesirable effect on the scalp. Finally, the unpleasant odor of the reducing agents used requires extensive addition of perfume to the products.

[0005] Some of said problems can be solved by use of 2-mercaptopropionic acid (thiolactic acid). Compared to the generally used thioglycolic acid, however, thiolactic acid has a weaker shaping effect.

[0006] The mercaptocarboxylic esters which permit hair shaping also at low pH values are unsatisfactory in terms of their skin tolerance and sensitization risk. In place of mercaptocarboxylic esters, mercapto acid amides such as thioglycolic acid amide or alkyl-substituted and hydroxyalkyl-substituted amides can be used. Such compounds are known from patents WO-A-91/10421 and EP-A-0 455 457. Like the carboxylic esters, these compounds have a high shaping potential also at low pH values, but in terms of their sensitizing properties are even worse than the esters.

[0007] The purpose of the invention is therefore to provide an agent and a method for permanent hair shaping which both in the acidic and in the alkaline range (pH=4.0 to 9.0) makes it possible to achieve uniform shaping and which has no sensitizing potential.

[0008] Surprisingly, we have now found that the said drawbacks can be avoided by use of N,N-disubstituted mercaptoacetamides having the following formula (I) and that these mercaptoacetamides have a higher shaping potential than thiolactic acid.

[0009] Hence, the object of the present invention is an agent for the permanent shaping of hair, characterized in that it contains as the keratin-reducing active ingredient a compound having the general formula 2

[0010] or a salt thereof, wherein R1 and R2 denote a straight-chain or branched alkyl, monohydroxyalkyl or polyhydroxyalkyl or carboxyalkyl group, each with 1 to 6 carbon atoms.

[0011] Suitable salts of the mercaptoacetamides of formula (I) are all physiologically tolerated salts, particularly the hydrochloride, sulfate, phosphate, lactate, citrate and acetate.

[0012] Preferred are compounds in which R1 and R2 independently of each other denote CH3, CH2CH3, CH2CH2CH3, CH(CH3)2, C(CH3)3, CH2CH(CH3)CH3, CH(OH)CH3, CH2OH, CH2CH2OH, CH2CH(OH)CH3, CH2CH2CH2OH, CH2CH(OH)CH2OH, CH(CH3)(CH2OH), CH(CH2OH)2 or CH2COOH.

[0013] Particularly preferred are compounds having the formulas 3

[0014] The mercaptoacetamides of formula (I) are present in the ready-for-use hair shaping agent in an amount from 3 to 28 wt % and preferably from 5 to 21 wt %.

[0015] In another embodiment of the invention, the mercaptoacetamides of formula (I) can also be used in admixture with other, known thiols, such as thioglycolic acid, thiolactic acid, cysteine, cysteamine and alkyl- or acylcysteamines or sulfites.

[0016] The ready-for-use hair shaping agents preferably have a pH of 4.5 to 9.5 a pH of 6.5 to 8.5 being particularly preferred. Suitable alkalizing and pH-adjusting agents are, in particular, ammonia or sodium hydroxide, but also water-soluble, physiologically tolerated salts of organic and inorganic bases, for example, ammonium hydrogen carbonate.

[0017] For marketing purposes, the shaping agents can be packaged as a one-component or a two-component system, the agent possibly being in the form of an aqueous solution or an emulsion or else in thickened, aqueous form, particularly as a cream, gel, foam or paste.

[0018] Naturally, the shaping agent can contain all known additives commonly used for such agents, for example, thickeners such as bentonite, fatty acids, starch, polyacrylic acid and derivatives thereof, cellulose derivatives, alginates, vaseline, paraffin oils; wetting agents or emulsifiers from the class of anionic, cationic, amphoteric or nonionic surface-active substances, for example fatty alcohols, fatty alcohol ether sulfates, alkylsulfonates, alkylbenzenesulfonates, quaternary ammonium salts, alkylbetaines, ethoxylated alkylphenols, fatty acid alkanolamides or ethoxylated fatty acid esters; moreover, opacifying agents, such as, for example, polyethylene glycol esters; alcohols, such as, for example, ethanol, propanol, polyols such as, for example, 1,2- or 1,3-propanediol, 1,2-, 1,3- or 1,4-butanediol, 1,2-, 1,3-, 1,4- or 1,5-pentanediol and glycerol; sugars such as, for example, D-glucose; solubilizers, stabilizers, buffers, scented oils, dyes and hair-conditioning and hair-care constituents, such as, for example cationic polymers, lanolin derivatives, cholesterol, pantothenic acid and betaine.

[0019] The said constituents are used in amounts commonly employed for such purposes. For example the wetting agents and emulsifiers are used at a total concentration of 0.2 to 30 wt %, the alcohols in a total amount of 0.1 to 20 wt %, the opacifying agents, scented oils and dyes in an amount of 0.01 to 1 wt % each, the buffers in a total amount of 0.1 to 10 wt %, sugar, solubilizers, stabilizers and hair-conditioning and hair-care agents in an amount of 0.1 to 5 wt % each, whereas the thickeners and solubilizers can be contained in said agent in a total amount of 0.5 to 20 wt %.

[0020] Moreover, for the purpose of enhancing the shaping agent's efficacy, it is possible to add to it swelling agents and penetrants, for example dipropylene glycol monomethyl ether, 2-pyrrolidone or imidazolidin-2-one in an amount of 1 to 30 wt %, and for the purpose of preventing excessively tight hair curling dithio compounds, for example dithioglycolic acid, dithiolactic acid, the disulfides of said compounds or their salts.

[0021] By varying the pH, it is possible to provide an agent universally suitable for any hair structure, such an agent optionally being used in conjunction with heat. The agent brings about elastic, lasting and uniform shaping from the root to the tip of the hair without inducing allergic or sensitizing reactions.

[0022] Moreover, the present invention relates to a method for permanent hair shaping whereby the hair, before and/or after it was brought into the desired shape, is treated with a shaping agent, rinsed with water, treated with an oxidant, rinsed with water, optionally shaped to a wave using water only and then dried, said method being characterized in that the afore-described agent of the invention is used as the shaping agent.

[0023] According to a preferred embodiment of the method of the invention, the hair is first washed with a shampoo and then rinsed with water. The towel-dried hair is then divided into individual strands and wrapped onto a curler with a diameter of 5 to 30 millimeters and preferably 5 to 15 millimeters. The hair is then treated with an amount of the described shaping agent of the invention sufficient for hair shaping, preferably with 60 to 120 grams.

[0024] After a period of time sufficient for permanent shaping of the hair which, depending on the hair structure, pH, shaping efficacy of the shaping agent and use temperature, lasts from 5 to 30 min (10 to 30 min if no heat is used; 5 to 20 min with heating), the hair is rinsed with water and then post-treated (“fixed”) with an oxidant. The post-treatment agent is preferably used in an amount of 80 to 100 grams, depending on hair fullness.

[0025] For the oxidizing post-treatment in the wrapped or unwrapped state, any post-treatment agent suitable for such treatment can be used. Examples of oxidants that can be used in such post-treatment agents are potassium and sodium bromate, sodium perborate, urea peroxide and hydrogen peroxide. The concentration of the oxidant varies depending on the application time (as a rule 5 to 15 min) and the application temperature. The oxidant is usually present in the ready-for-use aqueous post-treatment agent at a concentration of 0.5 to 10 wt %. The agent for the oxidizing post-treatment can, of course, also contain other substances, for example wetting agents, care materials such as cationic polymers, weak acids, buffers or peroxide stabilizers, and it can be in the form of an aqueous solution, an emulsion or in thickened form on an aqueous basis, particularly as a cream, gel or paste. In particular, these common additives can be contained in the post-treatment agent in an amount of 0.1 to 10 wt %.

[0026] The curlers are then removed. If necessary, the unwrapped hair is subjected to another oxidizing treatment. The hair is then rinsed with water, optionally set to a wave using water only and then dried.

[0027] Another object of the invention is a method for making the mercaptoacetamides of formula (I) whereby an appropriate secondary amine is made to react with methyl thioglycolate at a temperature not exceeding 30° C. Said method is described more closely in Preparation Example 1, method A, and Preparation Examples 2, 4 and 5.

[0028] Yet another object of the invention is the novel N-ethyl-N-2′-hydroxyethylmercaptoacetamide, obtained by the afore-described method.

[0029] The following examples will explain the invention in greater detail without limiting the scope of the invention to these examples.

EXAMPLE 1

Preparation of the Mercaptoacetamides by Method A

[0030] Two moles of the appropriate primary amine was charged to a 500-mL three-necked flask. One mole of methyl thioglycolate was then slowly added dropwise with water-bath cooling so that the temperature did not exceed 30° C. The batch was flushed with argon and allowed to agitate until the methyl thioglycolate had quantitatively reacted (check by thin layer chromatography on 5×10 cm Merck DC-aluminum sheets; silica gel 60 F 254).

[0031] The mixture was acidified with 36% hydrochloric acid with ice cooling (pH 2-4) and exhaustively extracted with ethyl acetate. The solvent was distilled off under vacuum in a rotary evaporator, the residue was brought to pH 7.0 by addition of sodium hydroxide solution and again extracted by shaking with ethyl acetate. The combined fractions were dried over sodium sulfate and concentrated. The resulting residue was subjected to molecular distillation at 0.01 torr max. to give a virtually pure product. This procedure is of critical significance if it is desired to obtain as pure a product as possible in good yield. Because of their sensitizing properties, impurities consisting of incompletely reacted cleavage products formed by thermolysis or hydrolysis can be avoided only by careful distillation.

Preparation of Mercartoacetamides by Method B

[0032] In a 1-L three-necked flask, one mole of the appropriate primary amine was dissolved in 500 mL of water and cooled to 0° C. in an ice-water bath. To the solution was added 250 mL of 2 N NaOH, and one mole of chloroacetyl chloride was added dropwise so as not to exceed a temperature of 5° C. The batch was allowed to agitate vigorously at room temperature for three hours. To the mixture was then added one mole of potassium methylxanthogenate, and the mixture was allowed to agitate at room temperature for an additional twelve hours. The mixture was then acidified with 36% hydrochloric acid until a yellow oil separated. This oil was isolated and dissolved in a mixture of 500 mL of 25% ammonia and 250 mL of ethanol, and the resulting solution was allowed to agitate 1 hour at room temperature. The ethanol was then distilled off under vacuum in a rotary evaporator, and the residue was extracted with ethyl acetate. The aqueous phase was carefully acidified and once again extracted with ethyl acetate. The solvent was distilled off under vacuum in a rotary evaporator. The residue was then purified by distillation (see method A) or recrystallized from ethyl acetate. 1 TABLE 1 Elemental Analysis Standardized Wave Stability Mercaptoacetamide calculated HPLC Boiling WSN WSN WSN (amine component) Yield found area % point pH = 7 pH = 8 pH = 9 1) N,N-Dimethylmercaptoacetamide 73% C: 40,33, H: 7,56, 98,45% 73° C./ 81% 98% 98% N: 11,76, S: 26,92, 0,03 (Dimethylamine) C: 39,61, H: 7,41, Torr N: 11,53, S: 26,58 2) N,N-Diethylmercaptoacetamide 35% C: 48,94, H: 8,90, 99,19% 74° C./ 83% 98% 106%  N: 9,51, S: 21,78, 0,1 Torr (Diethylamine) C: 48,40, H: 8,89, N: 9,60, S: 21,83 3) N-Butyl-N-methylmercaptoacetamide 25% C: 52,14, H: 9,38, 99,19% 88° C./ 63% 67% 87% N: 8,69, S: 19,88, 0,075 (Butylmethylamine) C: 51,86, H: 9,03, Torr N: 8,85, S: 19,82 4) N-Ethyl-N-2′-hydroxyethylmercaptoacetamide 58% C: 44,15, H: 8,03 98,35% 108° C./ 78% 95% 99% N: 8,58, S: 19,64, 0,075 (N-ethyl-N-hydroxyethylamine) C: 44,21, H: 7,83, Torr N: 8,37, S: 19,30 Thiolactic acid for comparison 57% 50% 70% In material reproduced from the original, commas denote decimal points - Translator WSN = SWS = standardized wave stability - Translator

EXAMPLE 2

Preparation of N,N-Dimethylmercartoacetamide

[0033] 225 g (2 moles) of 40% aqueous dimethylamine solution was charged to a 500-mL three-necked flask. Then, 106.24 g of methyl thioglycolate was slowly added dropwise so as not to exceed a temperature of 30° C. The batch was flushed with argon and allowed to agitate 2 days at room temperature.

[0034] The mixture was acidified with 36% hydrochloric acid with ice cooling (pH 2-4) and exhaustively extracted with ethyl acetate. The solvent was distilled off under vacuum in a rotary evaporator and the residue was brought to pH 7.0 by addition of sodium hydroxide solution and once again extracted by shaking with ethyl acetate. The combined fractions were dried over sodium sulfate and concentrated. The residue was subjected to molecular distillation at 0.01 torr max. to obtain the pure product. The yield was 87 g (73%). 2 Analysis a) 1H-NMR (CDCL3): &dgr; (ppm) =  3,34 (s, 2H, HS—CH2—CO)  3,07 (s, 3H, N—CH3)  2,99 (s, 3H, N—CH3)  2,0 (broad, 1H, HS) b) 13C-NMR (CDCL3): &dgr; (ppm) = 169,42 (—C═O)  37,38 (N—CH3))  35,68 (N—CH3))  26,00 (HS—CH2) c) MS (70 e V, El, RT) m/z (%) = (M+) = 119 (40,06) 86 (14,4), 72 (100), 44 (46,46), d) Thiol titration: 95.36% e) Elemental analysis: C4H9NOS (mol. wt. 119.19) Calcd.: C 40.33, H 7.56, N 11.76, S 26.92 Found: C 39.61, H 7.41, N 11.53, S 26.58 f) IR (KBr) 2931 s (CH2) 2542 w (SH) 1644 s (N,N-disubstituted amide) g) HPLC HPLC gave 98.45 area percent for the compound. (column: C 18 5U, 250 mm × 4.6 mm; mobile phase acetonitrile:buffer [4 g KH2PO4 + 0.8 g sodium octanesulfonate + 2 mL H3PO4]; flow rate: 0.5 mL/min; wavelength 200 nm; = 25:75). h) pKa 7.92 (H2O) i) UV max. 210.4 nm (acetonitrile:buffer = 25:75) j) Boiling point 73° C./0.03 torr

EXAMPLE 3

Preparation of N,N-Diethylmercaptoacetamide

[0035] In a 1-L three-necked flask, 73 g (1 mole) of diethylamine was dissolved in 500 mL of water and cooled to 0° C. in an ice-water bath. To the solution was added 250 mL of 2 N NaOH, and then 112 g (1 mole) of chloroacetyl chloride was added dropwise so as not to exceed a temperature of 5° C. The batch was allowed to agitate vigorously for three hours at room temperature. Then, 160.3 g (1 mole) of potassium methylxanthogenate was added to the mixture, and the mixture was allowed to agitate for an additional twelve hours at room temperature. The mixture was acidified with 36% hydrochloric acid until a yellow oil separated. This oil was isolated and dissolved in a mixture of 500 mL of 25% ammonia and 250 mL of ethanol. The resulting mixture was allowed to agitate one hour at room temperature. The ethanol was then distilled off under vacuum in a rotary evaporator, and the residue was extracted by shaking with ethyl acetate. The aqueous phase was acidified with 36% hydrochloric acid with ice cooling (pH 2-4) and exhaustively extracted with ethyl acetate. The solvent was distilled off under vacuum in a rotary evaporator and the residue was brought to pH 7.0 by addition of sodium hydroxide solution and once again extracted with ethyl acetate. The combined fractions were dried over sodium sulfate and concentrated. The resulting residue was subjected to molecular distillation at 0.01 torr max.to obtain a pure product. The yield was 51.5 g (35%). 3 Analysis: a) 1H-NMR (CDCL3): &dgr; (ppm) =  3,3-3,4 (m + s, 6H, 2x N—CH2 + HS—CH2—CO)  2,1 (t, 1H, HS)  1,1-1,2 (2x d, 6H, 2x CH3) b) 13C-NMR (CDCL3): &dgr; (ppm) = 168,99 (C═O)  42,60 (N—CH2)  40,8 (N—CH2)  26,26 (HS—CH2)  14,47 + 12,86 (2x CH3) c) MS (70 e V, El, RT) m/z (%) = (M+) = 147 (22,76) 114 (74,1), 100 (35,41), 86(4,73), 72(100), 58 (46,3), 44 (38) d) Thiol titration: 98.56% e) Elemental analysis: C6H13NOS (mol. wt. 147.24 g/mole) Calculated: C 48.94 H 8.90 N 9.51 S 21.78 Found: C 48.40 H 8.89 N 9.60 S 21.83 f) IR (KBr) 2975-2935 s (CH2) 2545 w (SH) 1639 s (N,N-disubstituted amide) g) HPLC HPLC analysis gave 99.18 area percent for the compound. (Column: C 18 5U, 250 mm × 4.6 mm, mobile phase acetonitrile:buffer [4 g KH2PO4 + 0.8 g Na octane- sulfonate + 2 mL H3PO4] flow rate 0.5 mL/min; wavelength 200 nm; = 25:75) h) pKa 8.361 (H2O) i) UV max: 227 nm (acetonitrile:buffer = 25:75) j) Boiling point: 74° C./0.1 torr

EXAMPLE 4

Preparation of N-Butyl-N-Methylmercartoacetamide

[0036] 174 g (2 moles) of butylmethylamine was charged to a 500-mL three-necked flask and to it was slowly added dropwise 106.24 g of methyl thioglycolate so as not to exceed a temperature of 30° C. The batch was flushed with argon and allowed to agitate 2 days at room temperature. The mixture was acidified with 36% hydrochloric acid with ice cooling (pH 2-4) and exhaustively extracted with ethyl acetate. The solvent was distilled off under vacuum in a rotary evaporator and the residue was brought to pH 7.0 by addition of sodium hydroxide solution and once again extracted by shaking with ethyl acetate. The combined fractions were dried over sodium sulfate and concentrated. The resulting residue was subjected to molecular distillation at 0.01 torr max. to obtain the pure product. The yield was 40 g (25%). 4 Analysis: a) 1H-NMR (CDCL3): &dgr; (ppm) =  3,34-3,26 (m, 4H, HS—CH2—CO + N—CH2)  3,0-2,91 (2x d, 3H, N—CH3)  2,16 (broad | 1H, HS)  1,55-1,46 (m, 2H, N—CH2—CH2)  1,29-1,27 (m, 2H, CH2—CH2—CH2—CH3)  0,9 (2x t, 3H, CH3) b) 13C-NMR (CDCL3): &dgr; (ppm) = 169,67 + 169,56 (—C═O)  50,4 + 48,17 (N—CH2)  35,7 + 34,01 (N—CH3))  30,68 + 29,25 (N—CH2—CH2—CH2)  26,63 + 25,99 (HS—CH2)  20,02 (CH2—CH3)  13,88 (CH2—CH3) c) MS (70 e V, El, RT) m/z (%) = (M+) = 161 (19,29) 128 (28,9), 114 (23,5), 100 (11,23), 86 8(10,4), 57 (50,5), 44 (100) d) Thiol titration: 98.48% e) Elemental analysis: C7H15NOS (mol. wt. 161.26 g/mole) Calculated: C 52.14 H 9.38 N 8.69 S 19.88 Found: C 51.86 H 9.03 N 8.85 S 19.82 f) IR (KBr) 2930-2869 s (CH2) 2547 w (SH) 1643 s (N,N-disubstituted amide) g) HPLC HPLC analysis gave 99.19 area percent for the compound. (Column: C 18 5U, 250 mm × 4.6 mm, mobile phase acetonitrile:buffer [4 g KH2PO4 + 0.8 g Na octane- sulfonate + 2 mL H3PO4] flow rate 0.5 mL/min; wavelength 200 nm; = 25:75) h) pKa 7.873 (H2O) i) UV max: 230.8 nm (acetonitrile:buffer = 25:75) j) Boiling point: 88° C./0.075 torr

EXAMPLE 5

Preparation of N-Ethyl-N-2′-Hydroxyethylmercaptoacetamide

[0037] 168 g (2 moles) of N-ethyl-N-2′-hydroxyethylamine was charged to a 500-mL three-necked flask and to it was added slowly and dropwise 106.24 g of methyl thioglycolate so as not to exceed a temperature of 30° C. The batch was flushed with argon and allowed to agitate 2 days at room temperature. The mixture was acidified with 36% hydrochloric acid with ice cooling (pH 2-4) and exhaustively extracted with ethyl acetate. The solvent was distilled off under vacuum in a rotary evaporator and the residue was brought to pH 7.0 by addition of sodium hydroxide solution and once again extracted by shaking with ethyl acetate. The combined fractions were dried over sodium sulfate and concentrated. The resulting residue was subjected to molecular distillation at 0.01 torr max. to obtain the pure product. The yield was 95 g (58%). 5 Analysis: a) 1H-NMR (CDCL3): &dgr; (ppm) =  3,72 (m, 2H, CH2—OH)  3,41 (t, 1H, OH)  3,39-3,3 (m, 6H, HS—CH2—CO + 2x N—CH2)  2,14 (t, 1H, HS)  1,22-1,1 (2t, 3H, CH3) b) 13C-NMR (CDCL3): &dgr; (ppm) = 171,43 (—C═O)  61,63 (CH2—OH)  49,47 (N—CH2—CH2—OH)  44,55 (N—CH2—CH3)  26,01 (HS—CH2)  14,12 (CH3) c) MS (70 e V, El, 30° C.) m/z (%) = (M+) = 163 (52,22) 132 (31,7), 131 (77,9), 120 (18,99), 112 (16,14) 88 (52,5), 70 (34,22), 58 (100) d) Thiol titration: 98.03% e) Elemental analysis: C6H13NO2S (mol. wt. 163.23 g/mole) Calculated: C 44.15 H 8.03 N 8.58 S 19.64 Found: C 44.21 H 7.83 N 8.37 S 19.30 f) IR (KBr) 3407 s (OH) 2974-2849 (CH2) 2545 w (SH) 1625 s (N,N-disubstituted amide) g) HPLC HPLC analysis gave 98.35 area percent for the compound. (Column: C 18 5U, 250 mm × 4.6 mm, mobile phase acetonitrile:buffer [4 g KH2PO4 + 0.8 g Na octane- sulfonate + 2 mL H3PO4] flow rate 0.5 mL/min; wavelength 200 nm; = 25:75) h) pKa 7.604 (H2O) i) UV max: 234.4 m [sic - “nm” is meant - Translator] (acetonitrile:buffer = 25:75) j) Boiling point: 108° C./0.075 torr

EXAMPLE 6

Comparison of Waving Efficacy

[0038] The waving efficacy of 1-mercaptoacetamides was determined with the aid of waving solutions at pH 7, 8 and 9 using glycerol monothioglycolate for comparison. To this end, 16.5 cm-long strands of prebleached and thus damaged counted mid-European hair (about 100 hairs) were wrapped wet onto standardized spiral curlers (inner diameter: 3 millimeters) and after conditioning in a conditioning room (temperature: 20° C.; air humidity 65%) treated with a solution containing 87 mmol of reducing agent/100 g and adjusted to the indicated pH. The quantity of waving solution applied was calculated to conform to a 1:1.2 ratio (1 g of hair:1.2 mL of waving solution). The solution was allowed to act for 20 min at a temperature of 50° C. The hair was then fixed with a peroxide-containing fixing agent and dried. After unwrapping, the hair was suspended in water for 4 hours (water bath temperature: 40° C.).

[0039] Wave stability was calculated by the following expression: 1 Wave ⁢   ⁢ stability , % = I 0 - I t I 0 - I 1 I 0 =   ⁢ total ⁢   ⁢ length ⁢   ⁢ of ⁢   ⁢ unshaped , stretched ⁢   ⁢ strands ⁢   ⁢ ( 16.5 ⁢   ⁢ cm ) I t =   ⁢ length ⁢   ⁢ of ⁢   ⁢ unwrapped , suspended ⁢   ⁢ strands ⁢   ⁢ after ⁢   ⁢ 240 ⁢   ⁢ minutes I 1 =   ⁢ length ⁢   ⁢ of ⁢   ⁢ shaped , wrapped ⁢   ⁢ strands   ⁢ ( for ⁢   ⁢ a ⁢   ⁢ curler ⁢   ⁢ with ⁢   ⁢ an ⁢   ⁢ inner ⁢   ⁢ diameter ⁢   ⁢ of ⁢   ⁢ 3 ⁢   ⁢ mm ,   ⁢ this ⁢   ⁢ length ⁢   ⁢ is ⁢   ⁢ 35 ⁢   ⁢ mm ) .

[0040] Strands treated with a glycerol monothioglycolate solution adjusted to pH 9 were used as the standard. The standardized wave stability values (SWS) refer to this standard solution (pH 9) for which the wave stability was set at 100%.

[0041] Table 1 shows that the wave stabilities for the mercaptoacetamides according to the invention at pH 7, 8 and 9 are higher than those for thiolactic acid.

EXAMPLE 7

[0042] 6 Permanent Shaping Agent for Dyed Hair  10.5 g N,N-dimethylmercaptoacetamide  0.4 g ammonia (25% aqueous solution) for pH adjustment  2.0 g ammonium hydrogen carbonate  2.0 g dipropylene glycol monoethyl ether  1.0 g isooctylphenol, ethoxylated with 10 moles of ethylene oxide  1.0 g poly(dimethyldiallylammonium chloride)  0.3 g scented oil  0.1 g vinylpyrrolidone/styrene copolymer (Antara ® 430, GAF Corp., New York, USA)  84.7 g water 100.0 g

[0043] This agent had a pH of 7.3.

[0044] Hair previously damaged by dyeing treatments was washed with a shampoo, dried with a towel and wrapped onto curlers 8 mm in diameter. The afore-described hair shaping agent was then uniformly distributed over the wrapped hair. The hair was then covered with a plastic cap and warmed under a hood drier at a temperature of 45° C. for 10 minutes. The cap was then removed. The hair was rinsed with water and then subjected to an oxidizing post-treatment with a 3% aqueous hydrogen peroxide solution. After removal of the curlers, the hair was again rinsed with water, set to a wave using water only and then dried.

[0045] This treatment resulted in uniform, elastic and permanent shaping of the hair.

EXAMPLE 8

[0046] 7 Permanent Wave Agent for Normal Hair  15.9 g N,N-diethylmercaptoacetamide  8.9 g ammonia (25% aqueous solution)  5.0 g ammonium hydrogen carbonate  5.0 g isopropanol  5.0 g 1,2-propylene glycol  2.4 g monoethanolamine  1.5 g isooctylphenol, ethoxylated with 10 moles of ethyl- ene oxide  0.5 g poly(dimethyldiallylammonium chloride)  0.5 g scented oil  0.1 g vinylpyrrolidone/styrene copolymer (Antara ® 430, GAF Corp; New York, USA)  55.2 g water 100.0 g

[0047] This agent had a pH of 8.4.

[0048] Normal, not predamaged hair was washed, dried with a towel and wrapped onto curlers 6 mm in diameter. The hair was then uniformly moistened with the afore-described permanent wave agent. After a 15-min treatment period, the hair was thoroughly rinsed and then subjected to an oxidizing post-treatment with 80 g of a 3% aqueous hydrogen peroxide solution. After removal of the curlers, the hair was again rinsed with water, set to a wave using water only and then dried. This hair treatment produced uniform and bouncy curls.

EXAMPLE 9

[0049] 8 Permanent Wave Agent for Normal Hair  8.8 g N-ethyl-N-2′-hydroxyethylmercaptoacetamide  8.8 g N-butyl-N-methylmercaptoacetamide  5.0 g ammonia (25% aqueous solution) for pH adjustment  5.0 g ammonium hydrogen carbonate  5.0 g 1,2-pentanediol  2.0 g D-glucose  2.4 g ammonia  1.5 g isooctylphenol ethoxylated with 10 moles of ethylene oxide  0.5 g poly(dimethyldiallylammonium chloride)  0.5 g scented oil  0.1 g vinylpyrrolidone/styrene copolymer (Antara ® 430, GAF Corp., New York, USA)  60.4 g water 100.0 g

[0050] This agent had a pH of 8.3.

[0051] Normal, not predamaged hair was washed, dried with a towel and wrapped onto curlers 6 mm in diameter. The hair was then uniformly moistened with the afore-described permanent wave agent. After a 15-25 min treatment period, the hair was thoroughly rinsed and then subjected to an oxidizing post-treatment with 80 g of a 3% aqueous hydrogen peroxide solution. After removal of the curlers, the hair was again rinsed with water, set to a wave with water only and then dried. This hair treatment produced uniform and bouncy curls.

EXAMPLE 10

[0052] 9 Permanent Wave Agent for Normal Hair  17.5 g N-ethyl-N-2′-hydroxyethylmercaptoacetamide  8.0 g ammonia (25% aqueous solution) for pH adjustment  5.0 g ammonium hydrogen carbonate  5.0 g 1,2-pentanediol  2.4 g ammonia  1.5 g isooctylphenol ethoxylated with 10 moles of ethylene oxide  0.5 g poly(dimethyldiallylammonium chloride)  0.5 g scented oil  0.1 g vinylpyrrolidone/styrene copolymer (Antara ® 430, GAF Corp., New York, USA)  59.5 g water 100.0 g

[0053] This agent had a pH of 8.3.

[0054] Normal not predamaged hair was washed, dried with a towel and wrapped onto curlers 6 mm in diameter. The hair was then uniformly moistened with the afore-described permanent wave agent. After a 15-25 min treatment period, the hair was thoroughly rinsed and then subjected to an oxidizing post-treatment with 80 g of a 3% aqueous hydrogen peroxide solution. After removal of the curlers, the hair was again rinsed with water, set to a wave using water only and then dried. This hair treatment produced uniform and bouncy curls.

Claims

1. Agent for permanently shaping hair, characterized in that an N,N-disubstituted mercaptoacetamide having the general formula

4

or a salt thereof, wherein R1 and R2 denote a straight-chain or branched alkyl, monohydroxyalkyl, polyhydroxyalkyl or carboxyalkyl group each with 1 to 6 carbon atoms, is used as the keratin-reducing active ingredient.

2. Agent according to

claim 1, characterized in that in formula (I) R1 and R2 independently of each other denote CH3, CH2CH3, CH2CH2CH3, CH(CH3)2, C(CH3)3, CH2CH(CH3)CH3, CH(OH)CH3, CH2OH, CH2CH2OH, CH2CH(OH)CH3, CH2CH2CH2OH, CH2CH(OH)CH2OH, CH(CH3)(CH2OH), CH(CH2OH)2 or CH2COOH.

3. Agent according to one of claims 1 or 2, characterized in that the compound of formula (I) is contained in the ready-for-use agent in an amount from 3 to 28 wt %.

4. Agent according to one of

claims 1 to

4 [sic—“1 to 3” is meant—Translator], characterized in that the pH of the ready-for-use agent is 4.5 to 9.5

5. Agent according to one of

claims 1 to

4, characterized in that it is obtained before use by mixing two components.

6. N-Ethyl-N-2′-hydroxyethylmercaptoacetamide.

7. Method for permanently shaping hair whereby the hair is kept in the desired shape before and/or after being treated with a shaping agent, rinsed with water, subjected to an oxidizing post-treatment, optionally set to a wave using water only, and then dried, characterized in that the shaping agent used is one of the agents according to

claims 2 to

6.

8. Method according to

claim 7, characterized in that the shaping agent is allowed to act for 5 to 8 minutes.

9. Method according to

claim 8, characterized in that the shaping agent is allowed to act by use of heat for 5 to 20 minutes.

10. Method for producing the mercaptoacetamides of formula (I), characterized in that the appropriate primary or secondary amine is made to react with methyl thioglycolate at a temperature not exceeding 30° C.