Polyamino-polyamide crosslinked with crosslinking agent

Description

BACKGROUND OF THE INVENTION
It is known that the hair of many people, because of its general condition or because of repeated exposure to the atmosphere or to treatments such as bleachings, permanent wavings or dyeings, becomes degraded and often difficult to comb out or to set, especially in the case of a thick head of hair which is often dry, dull, rough or lacks vigor and liveliness.
Efforts heretofore have been made to limit or to correct these faults by applying to the hair a "hair conditioner" composition so as to improve the condition of moist and dry hair and to facilitate such operations as combing and setting the hair.
By "Hair conditioning" is meant an operation which, while facilitating the combing out of moist hair, also imparts to dry hair some swelling and elasticity, so as to assure good maintenance of the coiffure or style imparted thereto. The agents employed to achieve such "hair conditioning" are generally called "hair conditioners".
Conventionally there are employed in the conditioning of hair various synthetic polymers, such as polyethylene imines, polyvinylpyridines, the polychloride of p-vinylbenzyl trimethylammonium and the polychloride of diallyl dimethyl ammonium. However, it has also been found that these polymers suffer from the disadvantages of not being compatible with, for instance, anionic shampoo compositions.
It has also been known to use in the production of compositions for hair some polyamino-amide polymers, obtained by the polycondensation of a dicarboxylic acid and a polyalkylene polyamine, some polyaminoureylene polymers and some alkylene polyamine polymers modified particularly by epichlorohydrin in quantities near stoichiometric amounts relative to the amine groups of the polyamino-amide. However, the addition of these significant quantities of epichlorohydrin leads to the presence in the molecules of the crosslinked polymer some reactive groups. These polymers thus contain alkylating groups which are capable of reacting on nucleophilic groups such as amines, thiols, sulfates and the like. Representative of such alkylating groups are azetidinium rings. However, as a result of the presence of such reactive groups, the polymer lacks stability and generally degrades when put into solution. Further the presence of such alkylating groups renders cosmetic products incorporating the same of doubtful use for application to human skin.
There has also been recommended the use in a "hair conditioner" composition of heat crosslinkable thermosetting polymers, but their use necessarily involves a special heating step.
To avoid these drawbacks, there has been provided in our earlier applications Ser. Nos. 762,804 and 528,577, incorporated herein by reference, a chemically stable, crosslinked polyamino-polyamide free from reactive groups. This water-soluble crosslinked polymer is obtained by crosslinking a polyamino-polyamide which in turn is prepared by the polycondensation of an acidic compound on a polyamine. The acidic compound used is selected from the group consisting of:
(i) an organic dicarboxylic acid,
(ii) an ethylenically unsaturated aliphatic mono- or di-carboxylic acid,
(iii) an ester of said acids, preferably with a lower alkanol having from 1-6 carbon atoms, and
(iv) mixtures of these compounds.
The polyamine usefully employed to produce the polyamino-polyamide of our earlier applications is selected from the group consisting of bis-primary and mono- or bis-secondary polyalkylene-polyamines. From 0-40 mole percent of the selected polyamine can be replaced by a bis-primary amine, preferably, ethylenediamine or by a bis-secondary amine, preferably piperazine and 0-20 mole percent of the selected polyamine can be replaced by hexamethylene-diamine.
Crosslinking of the polyamino-polyamide in our earlier applications is effected with a crosslinking agent selected from the group consisting of epihalohydrins, diepoxides, dianhydrides, unsaturated anhydride and bis unsaturated derivatives, and is characterized by the fact that the crosslinking agent is employed in amounts of 0.025-0.35 mole of crosslinking agent per amine group of the polyamino-polyamide and generally from 0.025 up to about 0.2 mole and, in particular, from 0.025 to up to about 0.1 mole of crosslinking agent per amine group of the polyamino-polyamide.
Our earlier invention, as described in said Ser. Nos. 762,804 and 528,577 is also concerned with a hair conditioning cosmetic composition which comprises at least one water-soluble crosslinked polymer as defined above. This cosmetic composition is compatible with anionic shampoo compositions; it provides satisfactory combing out of moist hair and it imparts elasticity to dry hair thereby assuring good maintenance of the coiffure or style imparted to the hair.
The crosslinked polyamino-polyamidde present in the hair conditioning composition of our earlier invention exhibits the following characteristics: (1) it is perfectly soluble in water up to 10 water percent concentration without forming a gel; (2) the viscosity of such a 10% solution in water at 25.degree. C. is greater than 3 centipoises, the viscosity generally measuring between 3-200. More often the viscosity of such a solution is equal to or greater than 20 centipoises and lower than 50 centipoises; and (3) the polyamino-polyamide does not carry any reactive group and in particular it is chemically stable and does not have any alkylating characteristics.

DESCRIPTION OF THE INVENTION
The present invention is an improvement over our invention disclosed in said Ser. Nos. 762,804 and 528,577. Thus, it has now been found that by using different crosslinking agents, new crosslinked polyamino-polyamide polymers, as well as new cosmetic compositions for the hair containing these new polymers have now been provided.
In accordance with the present invention, the new polymers and the new compositions containing them exhibit relative to the polymers and to the hair compositions described in our earlier applications the advantage of imparting to the hair a better cosmetic state and principally of impartingto dry hair more body and elasticity, and improving or prolonging the maintenance of the hair style.
This advantage is more significant in the case of damaged hair having been submitted to successive bleachings and/or permanent wave treatments.
The new crosslinking agents employed in the present invention can be classified into the following three groups:
I--Simple bi-functional compounds selected from the group consisting of bis-halohydrins, bis-azetidinium, bis-haloacyl diamines and bis-alkyl halides;
II--Oligomers obtained by the reaction of compound (a) selected from the group consisting of the bi-functional compounds described in Group I aboveand the bi-functional crosslinking agents described in our earlier applications, i.e. epihalohydrins, bis-epoxides and bis-unsaturated derivatives, and specifically epichlorohydrin, N,N'-bis-epoxy propyl piperazine, diglycidyl ether, divinyl sulfone, methylene bis-acrylamide, on compound (b) which is a bi-functional compound reactive with compound (a);
III--The product of quaternization of a compound selected from the group consisting of compounds (a), described in the preceding paragraph, and theoligomers described in Group II which carry one or more tertiary amine groups totally or partially alkylatable with a known alkylating agent and in particular with an alkylating agent selected from the group consisting of chlorides, bromides, iodides, sulfates, mesylates and tosylates of methyl or ethyl, benzyl chloride or bromide, ethylene oxide, propylene oxide and glycidol.
More preferably the polymers of the present invention are produced using a crosslinking agent selected from the group consisting of
(I) simple bi-functional compounds selected from the group consisting of (1) bis-halohydrins resulting from the reaction of epihalohydrin with a primary amine, a bis-secondary diamine, a bis-phenol, or a bis-mercaptan, (2) bis-azetidinium, (3) bis-haloacyl diamines, (4) alkyl bis-halides of the formula ##STR1##where X=Cl or Br, Z represents ##STR2##x=1 to 3, m=0 or 1, n=0 or 1, m and n not representing 1 at the same time; moreover, when m=1, x=1; A.sub.1 represents a saturated divalent hydrocarbon radical having 2, 3, 4 or 6 carbon atoms or 2-hydroxy propylene;
(II) oligomers obtained by the reaction of compound (a) selected from the group consisting of compounds (1), (2), (3) and (4), each identified above, (5) epihalohydrins, (6) bis-epoxides and (7) bis-unsaturated derivatives with compound (b) which is a bi-functional compound reactive with compound (a) and selected from the group consisting of primary amines, bis-secondary diamines, bis-mercaptans and bis-phenols; the molar ratio of (b):(a) being between 0.1 and 0.9;
(II-bis) oligomers obtained by the reaction of compound (a.sub.1) selected from the group consisting of compounds (1), (3), (4) and (6) each identified above with a bis-tertiary diamine (b.sub.1) which is a bi-functional compound reactive with compound (a.sub.1); the molar ratio (b.sub.1):(a.sub.1) being between 0.1 and 0.9;
(III) the product of quaternization of a compound (a.sub.2) selected from the group consisting of (1) bis-halohydrins resulting from the reaction ofa epihalohydrin with piperazine, a bis-phenol or a bis-mercaptan, (2) bis-azetidinium, (3) bis-haloacyl diamines, (4) alkyl bis-halides of formula F.sub.1, above, (6) bis-epoxides, (7) bis-unsaturated derivatives,(8) oligomers of II above, obtained by the reaction of compound (a.sub.3) selected from the group consisting of compounds (1), (2), (3), (4), (6) and (7) each identified above with compound (b.sub.3) which is a bi-functional compound reactive with compound (a.sub.3) and selected from the group consisting of primary amines, bis-secondary diamines, bis-mercaptans and bis-phenols, the molar ratio (b.sub.3):(a.sub.3) being between 0.1 and 0.9, (9) oligomers obtained by the reaction of an epihalohydrin (compound a.sub.4) with a bi-functional compound (b.sub.4) selected from piperazine, bis-mercaptans, bis-phenols and bis-epoxides of piperazine, the molar ratio of (b.sub.4):(a.sub.4) being between 0.1 and 0.9; (10) oligomers obtained by the reaction of compound (a.sub.5) selected from the group consisting of (1) bis-halohydrins resulting from the reaction of an epihalohydrin with piperazine, a bis-phenol or a bis-mercaptan, (2) bis-haloacyl diamines, (3) alkyl bis-halides of formulaF.sub.1, above, and (4) bis-epoxides, with compound (b.sub.5) which is a bis-tertiary diamine, the molar ratio (b.sub.5):(a.sub.5) being between 0.1 and 0.9; the said product having at least one tertiary amine group which is alkylatable, with an alkylating agent (c) selected from the groupconsisting of chlorides, bromides, iodides, sulfates, mesylates and tosylates of methyl or ethyl, benzyl chloride or bromide, ethylene oxide, propylene oxide and glycidol.
The simple bi-functional compounds of Group I are more specifically:
(1') bis-halohydrins obtained by the reaction of an epihalohydrin, such as epichlorohydrin or epibromohydrin with a bi-functional compound such as bis-secondary diamines, primary amines, diols, bis-phenols or bis-mercaptans. These bis-halohydrins form very valuable crosslinking agents.
The bis-halohydrin resulting from the reaction of epichlorohydrin with piperazine is particularly valuable.
The bis-halohydrins can be direct intermediates for the preparation of bis-epoxides, but, inversely, they can be derived by opening the oxirane ring with an hydracid such as hydrochloric acid or hydrobromic acid.
In both cases, the halogen atom can be linked at the last carbon atom or the next-to-last carbon atom without its position being prejudicial to thereactivity of the crosslinking agent or to the properties of the final product.
Representative useful bis-halohydrins include the following: ##STR3##and in formulas (1)-(7), X represents Cl or Br.
(2') bis-azetidinium compounds derived from N,N-dialkyl halogeno hydroxy propylamines by cyclization. A representative bis-azetidinium is one made in accordance with the following reaction scheme: ##STR4##wherein X represents Cl or Br.
However, the cyclization can be difficult for certain sterically hindered amines.
As the reactivity of the azetidinium groups is only slightly different fromthat of epihalohydrin groups, there can be employed in the present invention compounds derived from bis-halohydrins for which the halohydrin units are linked to the remainder of the molecule by tertiary nitrogen groups, and carry two azetidinium groups or one azetidinium group and one halohydrin group;
(3') bis-haloacyl diamines useful as crosslinking agents can be representedby the formula: ##STR5##wherein X=Cl or Br, A=--CH.sub.2 --CH.sub.2 --, --CH.sub.2 --CH.sub.2 --CH.sub.2 -- or ##STR6##n represents a number between 1 and 10, R.sub.1 =R.sub.2 =H or R.sub.1 and R.sub.2 can be linked together and represent an ethylene radical; when ##STR7##R.sub.1 =R.sub.2 =H; when A represents --CH.sub.2 --CH.sub.2 --, R.sub.1 and R.sub.2 can be linked together and represent ethylene so that the group ##STR8##designates the radical ##STR9##which can be derived from piperazine.
Particularly useful bis-haloacyl diamines in the invention are the bis-chloroacetyl or the bis-bromo undecanoyl of ethylenediamine or of piperazine.
Particularly useful bis-epoxides are bis-epoxides of piperazine;
(4') oligomers, within the meaning of the present invention, are statistical mixtures of compounds obtained by the reaction of compound (a)described in Groups I and II or of a compound (a.sub.1) described in Group II-bis or of a compound (a.sub.3), (a.sub.4) or (a.sub.5) described in Group III with, respectively, a bi-functional compound (b), (b.sub.1), (b.sub.3), (b.sub.4), (b.sub.5) which are reactive with compounds (a), (a.sub.1), (a.sub.3), (a.sub.4), (a.sub.5) which are in a general fashion,primary amines, bis-secondary amines such as piperazine, bis-tertiary diamines such as N,N,N',N'-tetramethyl ethylene-, propylene-, butylene-, or hexamethylene-diamine, bis-mercaptans such as ethane 1,2-dithiol, or the bis-phenols such as Bis-phenol A or 2,2'-(4,4'-dihydroxy-diphenyl) propane.
The molar amount of (b), (b.sub.1), (b.sub.3), (b.sub.4) and (b.sub.5), relative, respectively, to (a), (a.sub.1), (a.sub.3), (a.sub.4) and (a.sub.5) is between 0.1 and 0.9.
The oligomerization reaction is generally carried out at temperatures between 0.degree. and 95.degree. C. and preferably between 0.degree. and 50.degree. C. in water, or in a solvent such as isopropanol, t-butanol, acetone, benzene, toluene, dimethylformamide or chloroform.
The quaternization reaction which provides the quaternization product described above, under III, is effected between 0.degree. and 90.degree. C. in water or in a solvent such as methanol, ethanol, isopropanol, t-butanol, alkoxy ethanols, acetone, benzene, toluene, dimethylformamide or chloroform.
Thus, the present invention relates to a crosslinked polyamino-polyamide polymer prepared by crosslinking a polyamino-polyamide, obtained by the polycondensation of an acidic compound selected from (i) organic dicarboxylic acids, (ii) aliphatic ethylenically unsaturated mono- and di-carboxylic acids, (iii) the esters of the said acids and (iv) mixtures of these compounds, on a polyamine selected from bis-primary and mono- or di-secondary polyalkylene-polyamines, 0 to 20 mole percent of this polyamine being able to be replaced by hexamethylene diamine, or 0 to 40 percent of this polyamine being able to be replaced by a bis-primary amine, preferably, ethylene diamine, or by a bis-secondary amine, preferably, piperazine. The crosslinking is effected using a crosslinking agent selected from the group consisting of:
(I) simple bi-functional compounds selected from the group consisting of (1) bis-halohydrins resulting from the reaction of an epihalohydrin with aprimary amine, a bis-secondary diamine, a bis-phenol or a bis-mercaptan (2)bis-azetidinium, (3) bis-haloacyl diamines, (4) alkyl bis-halides represented by the formula: ##STR10##wherein X=Cl or Br, Z represents ##STR11##x=1 to 3, m=0 or 1, n=0 or 1, m and n at the same time not representing 1; moreover when m=1, x=1; A.sub.1 represents a divalent saturated hydrocarbon having 2, 3, 4 or 6 carbon atoms or 2-hydroxy propylene;
(II) oligomers obtained by the reaction of compound (a) selected from the group consisting of compounds (1), (2), (3) and (4), each identified above, (5) epihalohydrins, (6) bis-epoxides and (7) bis-unsaturated derivatives; with compound (b) which is a bi-functional compound reactive with compound (a) and selected from the group consisting of primary amines, bis-secondary amines, bis-mercaptans and bis-phenols;
(II-bis) oligomers obtained by the reaction of compound (a.sub.1) selected from the group consisting of compounds (1), (3), (4) and (6) each identified above with a bis-tertiary diamine (b.sub.1) which is a bi-functional compound reactive with compound (a.sub.1); the molar ratio (b.sub.1):(a.sub.1) being between 0.1 and 0.9;
(III) the product of quaternization of compound (a.sub.2) selected from thegroup consisting of (1) bis-halohydrins resulting from the reaction of an epihalohydrin with piperazine, a bis-phenol or a bis-mercaptan, (2) bis-azetidinium, (3) bis-haloacyl diamines, (4) alkyl bis-halides of formula F.sub.1, (6) bis-epoxides, (7) bis-unsaturated derivatives, (8) oligomers II obtained by the reaction of compound (a.sub.3) selected from the group consisting of compounds (1), (2), (3), (4), (6) and (7) each identified above with compound (b.sub.3) which is a bi-functional compoundreactive with compound (a.sub.3) and selected from the group consisting of primary amines, bis-secondary diamines, bis-mercaptans and bis-phenols, the molar ratio (b.sub.3):(a.sub.3) being between 0.1 and 0.9, (9) oligomers obtained by the reaction of an epihalohydrin (compound a.sub.4) with a bi-functional compound (b.sub.4) selected from piperazine, bis-mercaptans, bis-phenols, bis-epoxides of piperazine; the molar ratio of (b.sub.4):(a.sub.4) being between 0.1 and 0.9; (10) oligomers obtained by the reaction of a compound (a.sub.5) selected from the group consistingof (1) bis-halohydrins resulting from the reaction of an epihalohydrin withpiperazine, a bis-phenol or a bis-mercaptan, (2) bis-haloacyl diamines, (3)alkyl bis-halides of formula F.sub.1 and (4) bis-epoxides with compound (b.sub.5) which is a bis-tertiary diamine, the molar ratio (b.sub.5):(a.sub.5) being between 0.1 and 0.9; said product having at least one tertiary amine group alkylatable with an alkylating agent (c) selected from the group consisting of chlorides, bromides, iodides, sulfates, mesylates and tosylates of methyl or ethyl, benzyl chloride or bromide, ethylene oxide, propylene oxide and glycidol.
The acids useful for the preparation of the polyamino-polyamide of the present invention are selected from organic saturated dicarboxylic acids having from 6 to 10 carbon atoms, for example adipic acid, 2,2,4-trimethyland 2,4,4-trimethyl adipic acids; terephthalic acid; aliphatic ethylenically unsaturated mono- and di-carboxylic acids, for example, acrylic acid, methacrylic acid and itaconic acid.
Among the preferred acids are adipic acid and the addition compounds of an alkylene diamine with an unsaturated acid such as acrylic acid, methacrylic acid and itaconic acid.
Adipic acid is particularly preferable.
The esters of the above mentioned acids can also be used. It is also possible to use mixtures of two or more carboxylic acids and their esters.
The polyamines useful for the preparation of the polyamino-polyamide of thepresent invention are selected from bis-primary and mono- or di-secondary polyalkylene-polyamines, for example, diethylene triamine, dipropylene triamine, triethylene tetramine and their mixtures.
The polycondensation is carried out in accordance with known procedures, bymixing the initial reactants; heating the resulting mixture to a temperature between 80.degree. and 250.degree. C., and preferably between 100.degree. and 180.degree. C., for 1 to 8 hours. The choice of the exact reaction time and temperature can depend on the choice of the particular reactants selected but the same is easily determined by those skilled in the art. After heating the reaction mixture at total reflux for 1/2 hour to 1 hour, the water or alcohol formed during the course of the polycondensation is removed at first at atmospheric pressure and then at subatmospheric pressure.
The polycondensation reaction is carried out under a nitrogen atmosphere toavoid any significant colorations and to facilitate the elimination of volatile substances.
In carrying out the polycondensation reaction preferably equimolar amounts of the dicarboxylic acid and amine are employed.
According to a preferred embodiment of the present invention, the polycondensation of the polyalkylene-polyamine selected preferably from diethylene triamine, triethylene tetramine, dipropylene triamine and mixtures thereof is effected with either (i) a carboxylic diacid, preferably adipic acid or its dimethyl ester, or (ii) the intermediate product of addition of one molecule of ethylene diamine and two molecules of the methyl ester of an ethylenically unsaturated acid such as methyl acrylate or methyl itaconate.
The addition reaction of ethylene diamine on the said unsaturated ester is carried out by mixing the reactants at a temperature between 5.degree.-80.degree. C. The polycondensation reaction is effected by heating the reactants for 30-60 minutes at reflux followed by eliminating the methyl alcohol formed, at a temperature of 120.degree.-150.degree. C.,or of the water formed at a temperature of 140.degree.-175.degree. C., initially under atmospheric pressure and finally under sub-atmospheric pressure of 15 mm of mercury.
The polyamino-polyamides (A) thus obtained have a viscosity in a 10% aqueous solution at 25.degree. C. lower than 3 centipoises.
The preferred polyamino-polyamides (A) of the present invention are characterized by repeating units of the formula
--OC--R--CO--Z-- (I)
wherein R represents a bivalent radical which is derived from the acid employed or from the addition product of the acid with a bis-primary or bis-secondary amine.
Representative preferred values for R includes ##STR12##
These radicals are derived, respectively, from terephthalic acid, adipic acid, the product of addition of ethylenediamine with acrylic acid, methacrylic acid and itaconic acid, or their esters;
Z is selected from the group consisting of:
(1) in amounts of 60-100 mole percent, the radical
--NH--(CH.sub.2).sub.x --NH].sub.n (III)
wherein (a) x=2 and n=2 or 3 or (b) x=3 and n=2, this radical being derivedfrom diethylene triamine, triethylene tetramine or dipropylene triamine;
(2) in amounts of 0-40 mole percent (a) the radical (II) above, in which x=2 and n=1, the said radical being derived from ethylenediamine, or (b) the radical ##STR13##which is derived from piperazine; and
(3) in amounts of 0-20 mole percent the radical --NH--(CH.sub.2).sub.6 --NH-- which is derived from hexamethylenediamine.
The polyamino-polyamides thus obtained are then crosslinked by the additionof a crosslinking agent selected from those described above.
The crosslinking reaction is effected at a temperature between 20.degree. C. and 90.degree.0 C. using initially 20 to 30% aqueous solutions of the polyamino-polyamide to which is added the crosslinking agent by very smallfractions until there is obtained a significant increase in the viscosity, but without, however, forming a gel which no longer is soluble in water. The concentration is then rapidly adjusted to 10% by the addition of waterand the reaction mixture is then cooled.
According to a preferred characteristic of the present invention, there is employed during the crosslinking of the polyamino-polyamide polymers, a crosslinking agent in amounts of 0.025 to 0.35 mole per amine group of thepolyamino-polyamide. An interesting category of crosslinked polymers is obtained by using from 0.025 to up to about 0.2 mole of crosslinking agentper amine group of the polyamino-polyamide. Another advantageous category of crosslinked polymers is obtained by using from 0.025 to up to about 0.1mole of crosslinking agent per amine group of the polyamino-polyamide.
The amount of crosslinking agent to use, which can vary according to the nature of the polyamino-polyamide and of the crosslinking agent can be easily determined by adding the desired crosslinking agent to an aqueous solution of the polyamino-polyamide until the viscosity of a 10% solution is at 25.degree. C. between 3 centipoises and the gel state while preserving its perfect solubility in water.
The crosslinked polymers according to the present invention keep well and are compatible with anionic surfactants while providing good untangling ofwet hair. This compatibility with anionic surfactants can again be improvedby alkylation of the secondary amine groups of the crosslinked polyamino-polyamides. The alkylation improves the water solubility of the crosslinked polyamino-polyamides, in the presence of anionic surfactants.
The following alkylating agents can be employed:
(1) an epoxide, for example, glycidol, ethylene oxide, or propylene oxide,
(2) an ethylenically unsaturated compound, for example, acrylamide and acrylic acid;
(3) chloroacetic acid; and
(4) an alkane sultone, for example, propane sultone or butane sultone.
The alkylation of the crosslinked polyamino-amides is carried out in an aqueous solution, at a concentration of 10 to 30% and at a temperature between 10.degree. and 95.degree. C.
The crosslinked polymers according to the present invention can be used in various cosmetic compositions for the hair, for the treatment of normal hair and more particularly for the treatment of sensitized hair. They can also be used in concentrations from 0.1 to 5 weight percent, preferably, from 0.2 to 2.5 weight percent and advantageously, from 0.3 to 1.3 weight percent in cosmetic compositions for the hair and more particularly in shampoo compositions, such as an anionic, cationic, non-ionic, amphoteric or zwitterionic shampoo composition, a shampoo-dye composition, a hair dyecomposition, a hair styling gel, a hair styling lotion, a "brushing" lotion, a hair setting lotion, a hair rinse lotion, a non-rinse hair reinforcing setting lotion, a hair restructuring lotion, and in such cosmetic compositions as anti-pellicular and anti-seborrheic compositions and permanent waving compositions.
The present invention thus also relates to a cosmetic composition for the hair containing at least one water-soluble crosslinked polymer obtained bycrosslinking a polyamino-polyamide prepared by the polycondensation of an acid compound selected from (i) organic dicarboxylic acids, (ii) aliphaticethylenically unsaturated mono- and di-carboxylic acids, (iii) esters of the said acids and (iv) mixtures of these compounds, on a polyamine selected from bis-primary and mono- or di-secondary polyalkylene-polyamines, 0 to 20 mole percent of this polyamine being ableto be replaced by hexamethylene diamine, or 0 to 40 percent of this polyamine being able to be replaced by a bis-primary amine, preferably, ethylene diamine or by a bis-secondary amine, preferably, piperazine; the crosslinking being carried out with the use of a crosslinking agent selected from the group consisting of
(I) a compound selected from the group consisting of (1) bis-halohydrins, (2) bis-azetidinium, (3) bis-haloacyl diamines and (4) alkyl bis-halides;
(II) oligomers obtained by the reaction of compound (a) selected from the group consisting of (1) bis-halohydrins, (2) bis-azetidinium, (3) bis-haloacyl diamines, (4) alkyl bis-halides, (5) epihalohydrins, (6) bis-epoxides and (7) bis unsaturated derivatives, with compound (b) which is a bi-functional compound reactive with compound (a);
(III) the product of quaternization of a compound selected from the group consisting of compound (a) and oligomers (II) and carrying tertiary amine groups alkylatable with an alkylating agent (c) selected from the group consisting of the chlorides, bromides, iodides, sulfates, mesylates and tosylates of methyl or ethyl, benzyl chloride or bromide, ethylene oxide, propylene oxide and glycidol.
The crosslinking is advantageously carried out by means of a crosslinking agent selected from the group consisting of:
(I) simple bi-functional compounds selected from the group consisting of (1) bis-halohydrins resulting from the reaction of an epihalohydrin with aprimary amine, a bis-secondary amine, a bis-phenol or a bis-mercaptan, (2) bis-azetidinium, (3) a bis-haloacyl diamine, (4) an alkyl bis-halide having the formula ##STR14##wherein X=Cl or Br, Z represents ##STR15##x=1 to 3, m=0 or 1, n=0 or 1, m and n not representing 1 at the same time; moreover, when m=1, x=1; A.sub.1 represents a saturated divalent hydrocarbon radical having 2, 3, 4 or 6 carbon atoms or 2-hydroxy propylene;
(II) oligomers obtained by the reaction of compound (a) selected from the group consisting of compounds (1), (2), (3) and (4) each identified above,(5) epihalohydrins, (6) bis-epoxides and (7) bis-unsaturated derivatives with compound (b) which is a bi-functional compound reactive with compound(a) and selected from the group consisting of primary amines, bis-secondarydiamines, bis-mercaptans and bis-phenols; the molar ratio (b):(a) being between 0.1 and 0.9;
(II-bis) oligomers obtained by the reaction of compound (a.sub.1) selected from the group consisting of compounds (1), (3), (4), and (6) each identified above with a bis-tertiary diamine (b.sub.1) which is a bi-functional compound reactive with compound (a.sub.1); the molar ratio (b.sub.1):(a.sub.1) being between 0.1 and 0.9;
(III) the product of quaternization of compound (a.sub.2) selected from thegroup consisting of (1) bis-halohydrins resulting from the reaction of an epihalohydrin with piperazine; bis-phenols or bis-mercaptans, (2) bis-azetidinium, (3) bis-haloacyl diamines, (4) alkyl bis-halides of formula F.sub.1 above, (6) bis-epoxides, (7) bis-unsaturated derivatives, (8) oligomers II obtained by the reaction of compound (a.sub.3) selected from the group consisting of compounds (1), (2), (3), (4), (6), and (7) each identified above with compound (b.sub.3) which is a bi-functional compound reactive with compound (a.sub.3) and is selected from the group consisting of primary amines, bis-secondary diamines, bis-mercaptans and bis-phenols, the molar ratio (b.sub.3):(a.sub.3) being between 0.1 and 0.9, (9) oligomers obtained by the reaction of an epihalohydrin (compound a.sub.4) with a bi-functional compound (b.sub.4) selected from piperazine,bis-mercaptans, bis-phenols and bis-epoxides of piperazine, the molar ratioof (b.sub.4):(a.sub.4) being between 0.1 and 0.9; (10) oligomers obtained by the reaction of compound (a.sub.5) selected from the group consisting of (1) bis-halohydrins resulting from the reaction of an epihalohydrin with piperazine, a bis-phenol or a bis-mercaptan, (2) bis-haloacyl diamines, (3) alkyl bis-halides of formula F.sub.1 above, and (4) bis-epoxides, with compound (b.sub.5) which is a bis-tertiary diamine, themolar ratio (b.sub.5):(a.sub.5) being between 0.1 and 0.9; said product carrying tertiary amine groups alkylatable with an alkylating agent (c) selected from the group consisting of the chlorides, bromides, iodides, sulfates, mesylates and tosylates of methyl or ethyl, benzyl chloride or bromide, ethylene oxide, propylene oxide and glycidol.
The cosmetic composition is characterized by the fact that the polyamino-polyamide is crosslinked by means of 0.025 to 0.35, or better from 0.025 to about 0.2, or even better from 0.025 to about 0.1 mole of crosslinking agent per amine group of the polyamino-polyamide. The crosslinked polymer in the cosmetic composition of the present invention exhibits a combination of the following characteristics:
(1) it is perfectly soluble in water at 10% without formation of a gel;
(2) the viscosity of a 10% solution of polymer in water at 25.degree. C. isgreater than 3 centipoises; and
(3) it does not have any reactive groups and in particular it does not haveany alkylating properties and it is chemically stable.
The cosmetic compositions for the hair containing the crosslinked polymer of the present invention can have a pH between 2 and 11 and preferably between 3 and 8.
The cosmetic compositions for the hair according to the present invention before being applied to sensitized hair can include, advantageously, an electrolyte. The presence of the electrolyte in the composition reduces orsuppresses the tendency sensitized hair has to fix durably the polymers. Representative useful electrolytes include water-soluble alkali or alkaline earth salts of mineral or organic acids and preferably the chlorides and acetates of sodium, potassium, ammonium and calcium. The amount of electrolyte is not critical. Preferably the electrolyte is present in an amount between 0.01 and 5 weight percent and advantageously from 0.4 to 3 weight percent of the total weight of the composition. The ratio of electrolyte:polymer is between 0:1 and 1.5:1.
The cosmetic compositions for the hair can be colored and thus contain from0.001 to 0.5 weight percent of a dye based on the total weight of the composition. The cosmetic composition also conventionally contains a perfume in an amount of 0.1 to 0.5 percent by weight based on the total weight of the composition.
In the compositions of the present invention, the crosslinked polyamino-polyamide is present in an amount of 0.1 to 5 weight percent andpreferably 0.1 to 3 weight percent based on the total weight of the composition.
The cosmetic compositions for the hair in accordance with the present invention can be provided in the form of aqueous or alcoholic solutions, the alcohol being a lower alkanol such as ethanol or isopropanol, or in the form of a cream, a gel, a dispersion, or an emulsion.
In addition to the crosslinked polyamino-polyamide, the cosmetic composition can include, generally, various adjuvants conventionally employed in cosmetic compositions for the hair. The adjuvants generally present in these cosmetic compositions are, for example, perfumes, dyes, preservatives, sequesterants, thickening agents, emulsifiers, anionic, cationic, amphoteric, zwitterionic or non-ionic surfactants, synergists, softening agents, cosmetic polymers or resins and in particular non-ionic or cationic polymers or resins.
The cosmetic compositions for the hair, according to the present invention,constitute principally treating creams to be applied to the hair before or after dyeing or bleaching the same, before or after shampooing the hair, before or after a permanent waving of the hair; hair dye products; shampoos; rinse lotions to be applied before or after a shampoo; hair setting lotions; brushing lotions; and hair structuring lotions.
When the compositions of the present invention constitute a treating cream to be applied before or after dyeing or bleaching the hair, before or after shampooing the hair, before or after a permanent waving of the hair,the carriers for these creams are formulated from soaps or a fatty alcohol in the presence of emulsifiers. They can also contain fatty amides, glycerine, polymers, perfumes and dyes.
The pH of these creams is between 3 and 9 and preferably between 5 and 9.
The soaps can be constituted from natural or synthetic fatty acids having 12-18 carbon atoms, such as lauric acid, myristic acid, palmitic acid, oleic acid, ricinoleic acid, stearic acid and isostearic acid, in concentrations between 10 and 30% and alkalizing agents such as NaOH, KOH,ammonia, monoethanolamine, diethanolamine and triethanolamine.
Representative fatty amides include, in particular, the following compounds: mono- or diethanolamides of acids derived from copra, from lauric acid or from oleic acid, in concentrations between 0 and 10%.
Representative fatty alcohols include, in particular, oleyl alcohol, tetradecyl alcohol, cetyl alcohol, stearyl alcohol and isostearyl alcohol,in amounts between 0 and 10%.
The creams can also be formulated with natural or synthetic alcohols having12-18 carbon atoms in admixture with emulsifiers. Representative fatty alcohols include, in particular, the alcohol derived from the fatty acids of copra, tetradecyl alcohol, cetyl alcohol, stearyl alcohol and hydroxy stearyl alcohol, in concentrations between 5 and 25%.
Representative emulsifiers include the following:
non-ionic surfactants, such as oxyethylenated or polyglycerolated fatty alcohols, such as for example, oleyl alcohol polyoxyethylenated with 10 moles of ethylene oxide, cetyl alcohol oxyethylenated with 6 to 10 moles of ethylene oxide, cetyl stearyl alcohol oxyethylenated with 10 moles of ethylene oxide, stearyl alcohol oxyethylenated with 10-15 or 20 moles of ethylene oxide, oleyl alcohol polyglycerolated with 4 moles of glycerol and synthetic fatty alcohols having 9-15 carbon atoms polyoxyethylenated with 5 or 10 moles of ethylene oxide. These non-ionics are present in amount of 5 to 25 weight percent;
anionic surfactants, such as alkyl sulfates oxyethylenated or not, including sodium lauryl sulfate, ammonium lauryl sulfate, sodium cetyl stearyl sulfate, triethanolamine cetyl stearyl sulfate, monoethanolamine lauryl sulfate, sodium lauryl ether sulfate oxyethylenated with, for example, 2.2 moles of ethylene oxide and monoethanolamine lauryl ether sulfate oxyethylenated with, for example, 2.2 moles of ethylene oxide. These constituents are present in an amount between 3 and 15 weight percent.
Representative fatty amides include oleic diethanolamide, copra mono- or di-ethanolamide and stearic monoethanolamide. These amides are used in amounts between 0 and 10 weight percent.
When the compositions of the present invention constitute hair dye creams, they can include, in addition to the crosslinked polyamino-polyamide, various components recited in the above defined creams which impart a cream consistency to the composition. There is also included an alkalizingagent and a hair dye.
The pH of these compositions is generally between 9 and 11, the pH being regulated by the addition of an appropriate alkalizing agent in the dye support. For example ammonia, monoethanolamine, diethanolamine or triethanolamine can be added to the dye support or vehicle.
The hair dyes are oxidation dyes to which can be added direct dyes such as an azo, an anthraquinone, or a nitrobenzene dye, an indamine, an indoaniline, an indophenol or other oxidation dyes such as the leuco derivatives of these compounds.
When the compositions of the present invention constitute shampoo formulations, they include, in addition to the crosslinked polyamino-polyamide polymer, at least one anionic, cationic, non-ionic or amphoteric detergent.
Representative anionic surfactants include the following compounds, as wellas their mixtures:
the alkaline salts, the magnesium salts, the ammonium salts, the amine salts or the amino alcohol salts of the following compounds:
alkyl sulfates, alkyl ether sulfates wherein the alkyl has a C.sub.12 to C.sub.18 linear chain, ethoxylated alkylamide sulfates and ether sulfates with linear C.sub.12 to C.sub.18 chains, alkylaryl polyether sulfates and monoglyceride sulfates;
alkylsulfonates wherein the alkyl has a C.sub.12 to C.sub.18 linear chain, alkylamide sulfonates, alkylarylsulfonates and .alpha.-olefin sulfonates having C.sub.12 to C.sub.18 linear chains;
alkylsulfosuccinates, alkylethersulfosuccinates, and alkylamidesulfosuccinates wherein the alkyl moeity is a C.sub.12 -C.sub.18linear chain;
alkylsulfosuccinamates wherein the alkyl moiety is a C.sub.12 to C.sub.18 linear chain;
alkylsulfoacetates wherein the alkyl is a C.sub.12 to C.sub.18 chain;
alkyl phosphates and alkyletherphosphates wherein the alkyl is a C.sub.12 to C.sub.18 chain;
alkylsarcosinates, alkylpolypeptidates, alkylamidopolypeptidates, alkylisethionates and alkyl taurates wherein the alkyl is a C.sub.12 to C.sub.18 chain; and
fatty acids such as oleic acid, ricinoleic acid, palmitic acid, stearic acid, the acids of copra oil, or of hydrogenated copra oil, carboxylic acids and carboxylic acids of polyglycol ethers of the formula Alk--(OCH.sub.2 --CH.sub.2).sub.n --OCH.sub.2 --CO.sub.2 H wherein Alk is a C.sub.12 to C.sub.18 linear chain and n is a whole number from 5 to 15.
Representative cationic surfactants include, alone or in admixture, the following materials:
salts of fatty amines, such as alkylamine acetates;
quaternary ammonium salts, such as alkyl dimethylbenzylammonium chloride orbromide, alkyl trimethylammonium chloride or bromide, alkyl methylhydroxyethylammonium chloride or bromide, dimethyldistearylammonium chloride or bromide and methosulfates of alkylamido ethyltrimethylammoniumchloride or bromide,
salts of alkylpyridinium, and
imidazoline derivatives.
Further, amine oxides having a cationic character such as alkyldimethylamine oxide or alkylaminoethyl dimethylamine oxide can also be used.
Representative non-ionic surfactants which can be used in admixture with the previously defined anionics, include:
condensation products of a mono alcohol, an .alpha.-diol, an alkylphenol oran amide with glycidol. Such products include, for example, compounds of the formula R--CHOH--CH.sub.2 --O--(CH.sub.2 --CHOH--CH.sub.2 --O).sub.n H, wherein R represents an aliphatic, cycloaliphatic or arylaliphatic radical having 7 to 21 carbon atoms and their mixtures, the aliphatic chains being able to have ether, thioether and hydroxymethylene groups and1.ltoreq.n.ltoreq.10; and compounds of the formula RO--C.sub.2 H.sub.3 O(CH.sub.2 OH)].sub.n H wherein R represents alkyl, alkenyl or alkaryl having from 8 to 22 carbon atoms and n represents a number between 1 and 10;
alcohols, alkylphenols or polyglycerolated or polyethoxylated fatty acids having a linear fatty C.sub.8 to C.sub.18 chain carrying most often from 2to 15 moles of ethylene oxide, for example lauryl alcohol polyoxyethylenated with 12 moles of ethylene oxide;
copolymers of the oxides of ethylene and propylene;
the condensates of ethylene oxide and propylene oxide on fatty alcohols;
polyethoxylated fatty amides;
polyethoxylated fatty amines;
ethanolamides;
esters of fatty acids of glycol;
esters of fatty acids of sorbitol; and
esters of fatty acids of sucrose.
Representative amphoteric surfactants which can be used include principally:
alkylamino mono- and di-propionates;
betaines, such as N-alkyl betaines, N-alkylsulfobetaines and N-alkylamidobetaines; and
cycloimidinium (alkylimidazolines).
All these detergents, as well as numerous others not mentioned here but nonetheless useful in the shampoos according to the present invention, arewell known and are described in the literature.
The compositions of the present invention in the form of shampoos can also contain various adjuvants such as for example perfumes, dyes, preservatives, thickening agents, foam stabilizers, softening agents and cosmetic resins.
Representative foam stabilizers include fatty amides and particularly copramono- or di-ethanolamides, and lauric mono- or di-ethanolamides.
In these shampoo formulations, the detergent concentration is generally between 3 and 50 weight percent relative to the total weight of the composition, and preferably from 3 to 20 weight percent, and the pH is generally between 3 and 9.
When the compositions of the present invention constitute lotions, they canbe styling lotions, forming lotions (called "brushing lotions"), non-rinse reinforcing hair setting lotions, rinsing lotions (called "rinses") and the like.
By a "brushing lotion" is meant a lotion which is applied after shampooing and which improves the styling of the hair which is effected on damp or moist hair with the aid of a brush, during the drying of the hair with theaid of a hand dryer.
By a non-rinse reinforcing hair setting lotion is meant a lotion which is applied after shampooing and before setting the hair and which lotion is not rinsed from the hair. This lotion facilitates setting the hair and improves the durability of the hair set.
These lotions include, in an aqueous, alcoholic or hydroalcoholic solution at least one crosslinked polyamino-polyamide such as defined above. They can also contain:
film forming polymers such as polyvinylpyrrolidone, copolymers of vinylpyrrolidone and vinyl acetate, copolymers resulting from the polymerization of vinyl acetate and vinyl alkl ether.
Representative preferred resins, include polyvinylpyrrolidone having a molecular weight of 10,000 to 70,000; copolymers of vinylpyrrolidone (VP) and vinyl acetate (VA) having a molecular weight of 30,000 to 200,000, theVP:VA ratio being between 30:70 and 70:30; and terpolymers of methyl methacrylate (15-25%)-stearyl methacrylate (18-28%) and dimethylaminoethylmethacrylate (52-62%) quaternized or not by methyl sulfate.
The composition can also contain: quaternary polyvinylpyrrolidone copolymers, such as for example a polymer having a molecular weight in theorder of 1,000,000 and sold under the mark "Gafquat 755", and a polymer having a molecular weight in the order of 100,000 sold under the mark "Gafquat 734"; graft cationic copolymers resulting from the copolymerization of 3 to 95 weight percent N-vinylpyrrolidone, from 3 to 95 weight percent dimethylaminoethyl methacrylate and 2 to 50 weight percent polyethyleneglycol such as those described in French Pat. No. 76 15 948; corresponding essentially to U.S. patent application Ser. No. 690.783 filed May 27, 1976, now U.S. Pat. No. 4,047,888; cationic polymersresulting from the condensation of piperazine or its derivatives (1) on bi-functional compounds such as alkyl or alkyl aryl dihalides, bisepoxides, epihalohydrins, and bis-unsaturated derivatives, (2) on a primary amine whose two hydrogen atoms can be substituted and which function as a bi-functional compound; (3) both on an epihalohydrin and on a hydroxylated amine such as diglycolamine, 2-amino-2-methyl-1,3-propanediol or on an amino acid such as glycocoll, quaternized celluloses such as "JR 400".
In these lotions, the polymer concentration is generally between 0.1 and 5 weight percent and preferably between 0.1 and 3 weight percent and the pH is generally between 3 and 9.
By rinse lotion is meant a lotion that is applied to the hair before or after a hair dyeing or bleaching operation, before or after a shampooing, or between successive shampooings, before or after a permanent wave operation, so as to obtain a conditioning effect of the hair. Such a lotion is rinsed from the hair after a short contact time therewith.
These cosmetic rinse compositions of the present invention can be in the form of aqueous or hydroalcoholic solutions containing or not surface active agents, or emulsions, or gels. Further these rinse compositions canbe pressurized in aerosol containers. The surfactants used in these rinse lotions are principally non-ionic or cationic surfactants such as those described in the shampoo compositions above and more particularly:
condensation products of a mono alcohol, an .alpha.-diol, an alkylphenol oran amide with glycidol; for example, compounds of the formula R--CHOH--CH.sub.2 --O--(CH.sub.2 --CHOH--CH.sub.2 --O).sub.n H wherein R represents an aliphatic, cycloaliphatic or arylaliphatic radical having 7 to 21 carbon atoms and their mixtures, the aliphatic chains being able to have ether, thioether and hydroxymethylene groups and 1.ltoreq.n.ltoreq.10; and compounds of the formula RO--[C.sub.2 H.sub.3 O(CH.sub.2 OH)].sub.n H wherein R represents alkyl, alkenyl or alkylaryl having 8 to 22 carbon atoms and n is 1 to 10;
alcohols, alkylphenols or fatty acids, polyethoxylated or polyglycerolated,having a C.sub.8 to C.sub.18 linear fatty chain, and having most often from2 to 15 moles of ethylene oxide.
The concentration of the surfactant in the rinse lotion can vary from 0 to 7 weight percent.
An anionic or amphoteric surfactant can also be included in these rinse lotions.
When the compositions are provided in the form of emulsions, they can be non-ionic or anionic. The non-ionic emulsions are constituted by a mixtureof oils, and/or waxes, fatty alcohols and polyethoxylated fatty alcohols, such as stearyl or cetyl stearyl alcohols polyoxyethylenated for example with 10 moles of ethylene oxide. Cationic surfactants such as for example those defined above can also be employed.
The anionic emulsions are constituted from soaps. Representative emulsions include the selfemulsifiable emulsion constituted by glycerine stearate, sold under the name IMWITOR 960K and emulsions constituted by a combination of glycerine monostearate with esters of citric acid or with fatty alcohols and lipopeptides or with alkaline stearates, sold respectively under the names LAMEFORM ZEM, PLM and NSM.
When the compositions are provided in the form of gels they contain thickening agents in the presence or not of solvents.
Representative thickening agents include sodium alginate or gum arabic or cellulose derivatives such as methyl cellulose, hydroxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, carboxymethyl cellulose or carboxylic polymers such as the "Carbopols". Thickening of the lotions can also be obtained by using polyethylene glycols and stearates or distearates of polyethylene glycols, or by using phosphoric esters and amines.
The concentration of the thickening agent can vary from 0.5 to 30 weight percent and preferably from 0.5 to 15 weight percent.
The pH of these rinse lotions varies generally from 2 to 9.5.
When the compositions of the invention constitute restructuring lotions, they contain products which reinforce the keratin chain of the hair.
Such products include methylol derivatives such as those described in French Pat. Nos. 1,527,085 and 1,519,979 corresponding essentially to U.S.Pat. No. 3,773,056.
The following non-limiting examples are given to illustrate the present invention. Unless otherwise stated, all parts and percentages are by weight.
EXAMPLES OF PREPARATION
EXAMPLE A--POLYCONDENSATION OF EQUIMOLAR AMOUNTS OF ADIPIC ACID AND DIETHYLENE TRIAMINE.
The resulting polymer is characterized by the following unit:
--OC--(CH.sub.2).sub.4 --CONH--(CH.sub.2 --CH.sub.2 --NH.sub.2).sub.2 --
To 619 g (6 moles) of diethylene triamine, there are added, with agitation and under a nitrogen atmosphere and over a 15 minute period, 876 g (6 moles) of adipic acid. The reaction mixture is then heated to 145.degree.-150.degree. C., the temperature at which condensation of wateris observed. The reaction mixture is maintained at reflux for 45 minutes atwhich time the water is removed by distillation, initially at ambient pressure for 2 hours and then under reduced pressure (15 mm Hg) for 1 hour. The heating temperature increases progressively up to 170.degree. C.
The product thus obtained is poured out hot. After cooling, the product is in the form of a hard and brittle resin. It is transparent, has a yellow green color and is completely soluble in water.
EXAMPLE IA
Preparation of a quaternized crosslinking agent of the formula ##STR16##
To 236 g of a chloroform solution containing 57.2 g (0.289 mole) of bis(epoxypropyl)piperazine, there are added, over a one hour period, 36.4 g (0.289 mole) of dimethyl sulfate while maintaining the reaction mixture under agitation at 30.degree. C.
The quaternized derivative is then precipitated from its solution in a large excess of ether. After drying, there is recovered a very viscous oil, having an epoxide titer of 5.19 meq/g.
EXAMPLE IB
Crosslinking, with the crosslinking agent in Example IA, the polyamino-polyamide polymer obtained by condensation of adipic acid on diethylene triamine.
To 500 g of an aqueous solution containing 100 g (0.585 amine equivalent) of polyamino-polyamide prepared by condensation of equimolar amounts of adipic acid and diethylene triamine, according to Example A, there are added, at ambient temperature, 22 g (0.057 mole) of quaternized crosslinking agent prepared in Example Ia. The temperature of the reactionmedium is then raised to 90.degree. C.
After 20 minutes, gelling of the solution is observed. There are then rapidly added 698 g of water whereby a clear solution, yellow green in color, having 10% active material is obtained. The viscosity of this solution measured at 25.degree. C. is 0.68 p at 87.93 sec..sup.-1.
EXAMPLE IIA
Preparation of a quaternized crosslinking agent of the formula ##STR17##
To 187.3 g of a chloroform solution containing 54.9 g (0.277 mole) of bis(epoxypropyl)piperazine, there are added, over a 1 hour period, 70 g (0.555 mole) of dimethyl sulfate, while maintaining the reaction medium under agitation at 30.degree. C.
The medium thickened during the course of the addition and solidifies afterseveral hours at ambient temperature. The past is dissolved hot in dimethylformamide. When cold, the solution gives up white crystals having a meltingpoint of 205.degree. C., for which the epoxide index is 4.25 meg/g.
EXAMPLE IIB
Crosslinking, with the crosslinking agent prepared in Example IIA, the polyamino-polyamide polymer obtained by the condensation of adipic acid ondiethylene triamine is prepared.
To 476 g of an aqueous solution containing 95.2 g (0.557 amine equivalent) of the polyamino-polyamide prepared in Example A, there are added, at ambient temperature, 20 g (0.0425 mole) of the crosslinking agent preparedin Example IIA. The reaction mixture is maintained with agitation at 90.degree. C. for 1 hour. Then the solution is adjusted to 10% active material by the addition of 656 g of water.
The solution is clear and has a yellow green color. Its viscosity, measuredat 25.degree. C. is 0.27 p at 87.98 sec..sup.-1.
EXAMPLE IIIA
Preparation of a bis-unsaturated oligomer crosslinking agent obtained from piperazine bis-acrylamide and piperazine in molar porportions of 3/2 and having the formula: ##STR18##
To 380 g of an aqueous solution containing 194 g of bisacrylamide (1 mole) there are added, over a one hour period, and between 10 and 15.degree. C.,223 g of an aqueous solution containing 56.8 g (0.66 mole) of piperazine. The reaction medium is then left to stand for 24 hours at ambient temperature. The solution is cloudy and thickens. It is clarified by heating and is then poured slowly into 5 liters of acetone. The crosslinking agent precipitates. After filtration and drying, a white solid of which the dry extract is 80% is recovered.
EXAMPLE IIIB
Crosslinking, with the crosslinking agent prepared in Example IIIA, the polyamino-polyamide polymer obtained by condensation of adipic acid on diethylene triamine is prepared.
To 370 g of an aqueous solution containing 111 g (0.649 amine equivalent) of the polyamino-polyamide prepared according to Example A, there are added, at ambient temperature, 50 g of the crosslinking agent prepared in EXAMPLE IIIA. The temperature of the reaction medium is then raised to 90.degree. C. After 30 minutes the medium gels. The solution is rapidly adjusted to 10% dry extract by the addition thereto of 1050 g of water.
A clear, yellow green solution is obtained. The viscosity of this solution measured at 25.degree. C. is equal to 58 centipoises.
EXAMPLE IVA
Bis-halohydrin oligomer crosslinking agent prepared from epichlorohydrin and piperazine in molar proportions of 5/4 and having the formula ##STR19##where n=4.
To 541 g of an aqueous solution containing 69.4 g (0.806 mole) of piperazine, there are added, over a 1 hour period, without exceeding 20.degree. C., 92.5 g (1 mole) of epichlorohydrin. The reaction mixture isagain maintained for 1 hour with agitation at 20.degree. C.; then at the same temperature there are added 60 g (0.6 mole) of 40% NaOH over a 1 hourperiod.
EXAMPLE IVB
Crosslinking, with the crosslinking agent prepared in Example IVA, the polyamino-polyamide polymer obtained by the condensation of adipic acid ondiethylene triamine is prepared.
To 787.5 g of an aqueous solution containing 157.5 g (0.92 amine milliequivalent) of the polyaminopolyamide prepared in Example A, there are added, at ambient temperature, 268 g of an aqueous solution containing54.9 g of the crosslinking agent prepared in Example IVa. The temperature of the reaction medium is maintained for 4 h 50 min at 90.degree. C. At this point, the reaction medium gels. By rapid addition of 1100 cc of water there is obtained a clear solution having 9.85% active material. Theviscosity of this solution, measured at 25.degree. C. is equal to 73 centipoises.
EXAMPLE VA
Preparation of a quaternized crosslinking agent having the formula ##STR20##wherein n=4.
To 330 g of an aqueous solution containing 67.7 g (0.752 amine equivalent) of the crosslinking agent prepared in Example IVA, there are added, over a1 hour period and without exceeding 30.degree. C., 47.4 g (0.376 mole) of dimethylsulfate. The reaction medium is maintained with agitation for an additional 2 hours at this temperature.
EXAMPLE VB
Crosslinking, with a crosslinking agent prepared in Example Va, the polyamino-polyamide polymer obtained by the condensation of adipic acid ondiethylene triamine is prepared.
To 327.7 g of an aqueous solution containing 65.5 g (0.383 amine equivalent) of the polyamino-polyamide prepared in Example A, there are added, at ambient temperature, 155 g of an aqueous solution containing 47.25 g of the crosslinking agent prepared in Example Va. After 4 hours ofheating at 85.degree. C., the reaction mixture gels.
By rapid addition of 645 g of water, there is obtained a clear solution having 10% active material. The viscosity of this solution measured at 25.degree. C. is 0.47 poise at 67.18 sec..sup.-1.
EXAMPLE VIA
Preparation of bis-azetidinium crosslinking agent of the formula ##STR21##
To 50 g (0.212 mole) of 1,3-bis piperazine-2-propanol, (prepared by the addition of epichlorohydrin to piperazine - as described in Example 15 of French application No. 74 42279 of Nov. 28, 1972, or in Example 15 of U.S.Pat. No. 3,917,817) dissolved in 100 g of absolute ethyl alcohol, there areadded at a temperature between 0 and 5.degree. C., 43.5 g (0.47 mole) of epichlorohydrin. The reaction mixture is left to stand 24 hours at 0.degree. C. The crosslinking agent is then precipitated from its solutionin a large excess of ether. A white solid having a softening point of about120.degree. C. is isolated.
EXAMPLE VIB
Crosslinking, with a crosslinking agent, prepared in Example VIa, the polyamino-polyamide polymer obtained by the condensation of adipic acid ondiethylene triamine is prepared.
To 386 g of an aqueous solution containing 77.2 g (0.452 amine equivalent) of the polyamino-polyamide prepared in Example A, there are added, at ambient temperature, 15.4 g (0.036 mole) of the crosslinking agent prepared in Example VIa. After 2 hr. 30 min. of heating at 90.degree. C., the reaction medium gels. By rapid addition of 525 g of water, there is obtained a clear solution having 10% active material. The viscosity of this solution measured at 25.degree. C. is 0.7 poise at 67.18 sec..sup.-1.
EXAMPLE VIIA
Preparation of bis-(chloracetyl)piperazine crosslinking agent of the formula: ##STR22##
This crosslinking agent is prepared by condensing 2 molecules of chloracetyl chloride on a molecule of piperazine in the presence of NaOH.
EXAMPLE VIIB
Crosslinking, with the crosslinking agent prepared in Example VIIa, the polyamino-polyamide polymer obtained by the condensation of adipic acid ondiethylene triamine is prepared.
To 100 g of an aqueous solution containing 200 g (1.170 amine equivalents) of the polyamino-polyamide prepared in Example A, there are added, at ambient temperature, 24 g (0.1 mole) of bis-(chloracetyl)piperazine. The temperature of the reaction medium is then raised to 90.degree. C. After 30 minutes of heating the reaction medium gels. Then 1216 g of water are rapidly added and heating is continued at 80.degree. C. for 1 hour. A clear solution is obtained having 10% active material. The viscosity of this solution measured at 25.degree. C. is 0.29 poise at 88.41 sec..sup.-1.
EXAMPLE VIIIA
Preparation of bis-(1,1-bromo undecanoyl)piperazine crosslinking agent of the formula ##STR23##
This crosslinking agent is prepared by the condensation of 2 molecules of bromoundecanoyl bromide and one molecule of piperazine in the presence of sodium hydroxide.
EXAMPLE VIIIB
Crosslinking, with the crosslinking agent prepared in Example VIIIa, the polyamino-polyamide polymer obtained by the condensation of adipic acid ondiethylene triamine is prepared.
To 113.3 g of an aqueous solution containing 56.7 g (0.33 amine equivalent)of the polyamino-polyamide prepared in Example A, there are added, at ambient temperature, 60 g of an isopropanol solution containing 10 g (0.017 mole) of bis-(1,1-bromo undecanoyl) piperazine, prepared in ExampleVIIIa. The reaction medium is heated 2 hr. 30 min. at solvent reflux. The isopropanol is then distilled, while adding water until the attainment of a 10% aqueous solution of the resin (active material). The solution is slightly opalescent and its viscosity, measured at 25.degree. C. is 0.052 poise at 87.93 sec..sup.-1.
EXAMPLE IXA
Preparation of an oligomer crosslinking agent of the formula ##STR24##from epichlorohydrin and piperazine in molar proportions of 4/3.
To 1149 g of an aqueous solution containing 172 g (12 moles) of piperazine there are added, over a 1 hour period, 246.7 g (2.66 moles) of epichlorohydrin while maintaining the reaction mixture with agitation at 20.degree. C.
After an additional hour of agitation at 20.degree. C., there are added, atthe same temperature and in the space of 1 hour, 133 g (1.33 mole) of 40% NaOH. A precipitation in the course of neutralization is observed. There are then added 638 g of water and the mixture is heated a few minutes at 50.degree. C. to obtain a clear solution.
EXAMPLE IXB
Crosslinking, with the crosslinking agent prepared in Example IXA, the polyamino-polyamide polymer obtained by the condensation of adipic acid ondiethylene diamine.
To 2000 g of an aqueous solution containing 400 g (2.34 amine equivalents) of the polyamino-polyamide prepared according to Example A, there are added 584 g of an aqueous solution containing 99.8 g of the crosslinking agent prepared in Example IXA. The reaction medium is then maintained withagitation at 90.degree. C. for 5 hours. There are then added 2,414 g of water to obtain a clear solution having 10% active material. The viscosityof this solution measured at 25.degree. C. is 0.22 poise.
EXAMPLE XA
Preparation of an oligomer crosslinking agent of the formula: ##STR25##from epichlorohydrin and piperazine in molar proportions of 3/2.
To 1,221 g of an aqueous solution containing 172 g (2 moles) of piperazine there are added, over a 1 hour period and at 20.degree. C., 277.5 g (3 moles) of epichlorohydrin while maintaining the reaction mixture under agitation and at 20.degree. C. After an additional hour of agitation thereare added, at a temperature of 20.degree. C., 100 g (1 mole) of a 40% aqueous solution of NaOH.
On addition of 727.5 g of water and after a few minutes of heating, a clearsolution of the said crosslinking agent is obtained.
EXAMPLE XB
Crosslinking, with the crosslinking agent prepared in Example XA, the polyamino-polyamide polymer obtained by the condensation of adipic acid ondiethylene triamine is prepared.
To 2,000 g of an aqueous solution containing 400 g (2.34 amine equivalents)of the polyamino-polyamide prepared in accordance with Example A, there areadded 472 g of an aqueous solution containing 83.3 g of the crosslinking agent prepared in Example XA.
The reaction medium is maintained with agitation at 90.degree. C. and after4 hours of heating, the solution gels.
The solution is rapidly adjusted to 10% active material by the addition of 2,326 g of water.
A clear solution is obtained. The viscosity of this solution measured at 25.degree. C. is 0.64 poise at 88.4 sec..sup.-1.
EXAMPLES OF USE
EXAMPLE 1A
A rinse composition is prepared by admixing the following components:
______________________________________Compound of Example VIb 0.5 g active material ##STR26## 0.5 g active materialRCHOHCH.sub.2O(CH.sub.2CHOHCH.sub.2O).sub.nHwherein R = C.sub.9 -C.sub.10 alkyland n has a statisticalaverage value of 3.5 0.7gPhosphoric acid ester ofethoxylated oleylalcohol sold under thename "DIVALIN SO" 0.4gWater, sufficient for 100 cc______________________________________
The pH of this solution is 7-8. This rinse composition is applied to previously washed hair. The combing of the thus treated hair is excellent.The dry hair is particularly full, shiny and easy to style.
EXAMPLE IB
A rinse composition is prepared by admixing the following components:
______________________________________Polymer obtained by thecondensation of equimolaramounts of adipic acid anddiethylene triamine andcrosslinked with 0.11 moleof epichlorohydrin peramine group (according toExample 1a of S.N. 762,804) 0.5 g active materialCompound of Example VIIIb 0.5 g active materialR CHOHCH.sub.2O(CH.sub.2CHOHCH.sub.2O).sub.nHwherein R = C.sub.9 -C.sub.10 alkyl andn has a statistical averagevalue of 3.5 0.7 gPhosphoric acid ester ofethoxylated oleyl alcoholsold under the mark"DIVALIN SO" 0.4 gWater, sufficient for 100 cc______________________________________
The pH of this solution is 7-8. This rinse composition is applied to previously washed hair. The combing of the thus treated hair is excellent.The dry hair is particularly full, shiny and easy to style.
EXAMPLE 1c
An emulsion having the following composition is prepared:
______________________________________Petrolatum oil 15 gCetyl-stearyl alcohol, partiallysulfated, sold under themark "Cire de lanette" 2.5 gCetyl stearyl alcohol poly-oxyethylenated with 10moles of ethylene oxide,sold under the name"SIMULSOL 1951 RD" 2.5 gCompound of Example VIIb 0.7 gWater, sufficient for 100 g______________________________________
The pH of this solution is 9.5. Its application, followed by rinsing off this "rinse" in the form of an emulsion on the hair, facilitates its untangling; imparts to it softness; and gives good liveliness to the hair style.
EXAMPLE 1d
An emulsion having the following composition is prepared:
______________________________________Petrolatum oil 15 gCetyl stearyl alcohol, partiallysulfated, sold under themark "Cire de lanette" 2.5 gCetyl stearyl alcohol poly-oxyethylated with 10 molesof ethylene oxide, soldunder the name"SIMULSOL 1951 RD" 2.5 gCompound of Example IIIb 0.5 gWater, sufficient for 100 g______________________________________
The pH of this solution is 9. This "rinse" is applied to the hair, and leftin contact therewith for a few minutes. It is then rinsed off. The untangling of the hair is facilitated; the hair has a firmer touch; and the liveliness of the hair style is improved.
EXAMPLE 2a
A hair setting lotion is prepared by admixing the following components:
______________________________________ ##STR27## 0.5 g active materialCompound of Example VIb 0.5 g active materialQuaternary polyvinylpyrrolidonecopolymer having a molecularweight of about 100,000,sold under the name"GAFQUAT 734" 0.4 g active materialPerfume 0.2 gDyes 0.05 gWater, sufficient for 100 cc______________________________________
The pH of this lotion is 7.3. When applied to dyed hair, this hair setting lotion facilitates the combing of wet hair. The dry hair is soft and easy to style. This effect of softness lasts after several shampooings.
EXAMPLE 2b
The following hair setting composition is prepared:
______________________________________Compound of Example Ib 0.5 g active materialQuaternary polyvinylpyrrolidonecopolymer having a molecularweight of about 100,000, soldunder the name "GAFQUAT 734" 0.4 g active materialPerfume 0.1 gDyes 0.01 gWater, sufficient for 100 cc______________________________________
The pH of this composition is 7.3. When applied to dyed hair, this hair setting lotion facilitates the combing of wet hair. The dry hair is soft and easy to style. This effect of softness lasts after several shapooings.
EXAMPLE 2c
The following hair setting lotion is prepared:
______________________________________Compound of Example IIb 0.6 g active materialQuaternary polyvinyl-pyrrolidone copolymer havinga molecular weight of about100,000 and sold under thename "Gafquat 734" 0.5 gQuaternized cellulose soldunder the name"JR 400" 0.3 gEthyl alcohol, sufficient for 15.degree.Perfume 0.1 gWater, sufficient for 100 ccpH, adjusted to 8______________________________________
When applied to washed hair, this hair setting lotion facilitates combing. After drying and setting the hair, the hair is soft, shiny and is easy to style. This effect lasts after several shampooings.
EXAMPLE 2d
The following hair setting lotion is prepared:
______________________________________Compound of Example IVb 0.3 g active materialQuaternary polyvinylpyrrolidonecopolymer having a molecularweight of about 100,000 andsold under the name"Gafquat 734" 0.5 gQuaternary cellulose, soldunder the name "JR 400" 0.3 gEthyl alcohol, sufficient for 15.degree.Perfume 0.1 gWater, sufficient for 100 ccpH, adjusted to 8______________________________________
When applied to washed hair, this setting lotion facilitates combing. Afterdrying and setting, the hair is soft, shiny and easy to style. This effect last after several shampooings.
EXAMPLE 3a
The following "brushing lotion" is prepared:
______________________________________Compound of Example Vb 0.6 g active materialEthanol, sufficient for 10.degree.Dyes 0.1 gPerfume 0.1 gWater, sufficient for 100 gThe pH of this solution is adjusted to 7.______________________________________
EXAMPLE 3b
The following "brushing lotion" is prepared:
______________________________________Compound of Example IIIb 0.4 g active materialEthanol, sufficient for 10.degree.Dyes 0.1 gPerfume 0.1 gWater, sufficient for 100 ccThe pH of this solution is adjusted to 8.______________________________________
EXAMPLE 3c
The following "brushing lotion" is prepared:
______________________________________Compound of Example VIIIb 0.5 g active materialEthanol, sufficient for 20.degree.Dyes 0.2 gPerfume 0.1 gWater, sufficient for 100 ccThe pH of this solution is adjusted to 6.______________________________________
EXAMPLE 3d
The following "brushing lotion" is prepared:
______________________________________Compound of Example Ib 0.5 g active materialDyes 0.1 gPerfume 0.1 gWater, sufficient for 100 ccThe pH of this solution is adjusted to 5.______________________________________
EXAMPLE 3e
The following "brushing lotion" is prepared:
______________________________________Compound of Example IIb 0.8 g active materialEthanol, sufficient for 40.degree.Dyes 0.05 gPerfume 0.1 gWater, sufficient for 100 ccThe pH of this solution is adjusted to 7.______________________________________
EXAMPLE 3f
The following "brushing lotion" is prepared:
______________________________________Compound of Example VIIb 0.6 g active materialDyes 0.05 gPerfume 0.15 gWater, sufficient for 100 ccThe pH of this solution is adjusted to 6.______________________________________
The "brushing lotions" of Examples 3a-3f are applied to wet or dry hair after shampooing. The hair is styled using a brush, all while drying the hair with the aid of a hand dryer. Very good passage of the brush through the hair is noted as is a prolonged holding of the style. The hair thus treated is shiny and soft.
EXAMPLE 4a
The following shampoo composition is prepared:
______________________________________Triethanolamine C.sub.12 -C.sub.14alkyl sulfate 5 gRCHOHCH.sub.2O(CH.sub.2CHOHCH.sub.2O).sub.nHwherein R is C.sub.9 to C.sub.12 alkyland n has a statisticalaverage value of 3.5 5 gLauric diethanolamide 3 gCompound of Example VIb 1 gPerfume 0.1 gDyes 0.01 gWater, sufficient for 100 gpH adjusted to 8 with triethanolamine.______________________________________
This shampoo composition is provided in the form of a clear liquid. It facilitates combing wet hair and it imparts control and body to the hair.
EXAMPLE 4b
The following shampoo compositions is prepared:
______________________________________RCHOH CH.sub.2O(CH.sub.2CHOHCH.sub.2O).sub.nHwherein R is C.sub.9 to C.sub.12 alkyland n has a statisticalaverage value of 3.5 10 gCopra diethanolamide 3 gCompound of Example IIIb 1 g active materialWater, sufficient for 100 gThe pH of this composition initially was 8.7 andit was then adjusted to 6 using lactic acid.______________________________________
When applied to natural hair, this shampoo composition, provided in the form of a clear liquid, facilitates combing wet hair. The dry hair is fulland lively.
EXAMPLE 4c
The following shampoo composition is prepared:
______________________________________Ammonium lauryl sulfate 25 gDiethanolamide of the fattyacids of copra 2 gCompound of Example VIIIb 1 g active materialWater, sufficient for 100 gInitial pH of 8.1 adjusted to 7.7with lactic acid.______________________________________
When applied to dyed, permanent waved hair, this slightly opalescent clear shampoo composition produces convenient untangling of wet hair. After drying the hair is full and lively.
EXAMPLE 4d
The following shampoo composition is prepared:
______________________________________Lauryl alcohol poly-oxyethylenated with 12moles of ethylene oxide 5 gC.sub.12 -C.sub.18 alkyl dimethylcarboxymethyl ammoniumhydroxide, sold under thename "DEHYTON AB 30" 10 gLauric diethanolamide 3 gCompound of Example Ib 0.8 g active materialWater, sufficient for 100 gThe initial pH of 7.8 was adjusted to 6with lactic acid.______________________________________
When applied to dyed hair, this shampoo composition, provided in the form of a slightly opalescent clear liquid, facilitates the combing of wet hairand makes it softer. The dry hair is lively, full and controlled.
EXAMPLE 4e
The following shampoo composition is prepared:
______________________________________Triethanolamine C.sub.12 -C.sub.14alkyl sulfate 12.5 gLauric diethanolamide 2 gCompound of Example IIb 0.7 active materialWater, sufficient for 100 gpH = 7.4______________________________________
When applied to natural hair, this clear liquid shampoo composition provides good untangling of wet hair. The dry hair is full, lively and controlled.
EXAMPLE 4f
The following shampoo composition is prepared:
______________________________________C.sub.12 -C.sub.14 alcohol ethoxylatedwith 10 moles of ethyleneoxide and carboxymethylated,sold under the mark"AKYPO RLM 100" 3.5 gLauryl alcohol polyethoxylatedwith 12 moles ofethylene oxide 10 gCompound of Example IIB 0.6 g active materialHomopolymer of dimethyl diallylammonium chloride, M.W. =about 100,000, sold underthe mark "MERQUAT 100" 0.4 g active materialWater, sufficient for 100 gpH = 7.4______________________________________
When applied to dyed hair, this liquid shampoo composition improves the untangling of wet hair. The dry hair is controlled and shiny.
EXAMPLE 4g
A shampoo composition having the same formulation as that in Example 4f is prepared except that the 0.6 g of the compound of Example IIb is replaced by 0.5 g of the compound of Example VIIIb.
The properties of this shampoo composition are similar to those of the shampoo composition of Example 4f.
EXAMPLE 4h
The following shampoo composition is prepared:
______________________________________C.sub.12 -C.sub.14 alcohol ethoxylatedwith 10 moles of ethyleneoxide and carboxymethylated,sold under the mark"AKYPO RLM 100" 3.5 gLauryl alcohol polyethoxylatedwith 12 moles of ethylene oxide 10 gCompound of Example Ib 0.6 g active materialHomopolymer of dimethyl diallylammonium chloride, M. W. =about 100,000, sold under themark "MERQUAT 100" 0.4 g active materialPerfume 0.15 gDyes 0.02 gWater, sufficient for 100 gpH adjusted to 7______________________________________
When applied to dyed hair, this shampoo composition provides good untangling of wet hair and imparts to dry hair liveliness and fullness.
EXAMPLE 4i
The following shampoo composition is prepared:
______________________________________Hydroxy propyl methylcellulose 0.2 gDiethanolamide of thefatty acids of copra 3 gTriethanolamine C.sub.12 -C.sub.14alkyl sulfate 10 gCompound of Example VIIb 0.8 g active materialPerfume 0.15 gDyes 0.01 gWater, sufficient for 100 gpH, adjusted to 7.8______________________________________
When applied to natural permanent waved hair, this shampoo composition provides good untangling of wet hair and imparts to dry hair liveliness and fullness.
EXAMPLE 4j
The following shampoo composition is prepared:
______________________________________Lauryl alcohol polyethoxylatedwith 12 moles ofethylene oxide 7 gRCHOHCH.sub.2O(CH.sub.2CHOHCH.sub.2O).sub.nHwherein R = C.sub.9 to C.sub.12 alkyland n has a statisticalaverage value of 3.5 7 gDiethanolamide of coprafatty acids 2 gCompound of Example IVb 0.8 g active materialPerfume 0.1 gDyes 0.01 gWater, sufficient for 100 gpH, adjusted to 7.2______________________________________
When applied to dyed hair, this shampoo composition provides good untangling of wet hair and imparts to dry hair liveliness and fullness.
EXAMPLE 4k
The following shampoo composition is prepared:
__________________________________________________________________________RCHOHCH.sub.2O(CH.sub.2CHOHCH.sub.2OH).sub.nwherein R = C.sub.9 to C.sub.12 alkyland n has a statisticalaverage value of 3.5 10 gDiethanolamide of coprafatty acids 3 gCompound of Example IIb 0.5 g active material ##STR28## 0.2 g active materialWater, sufficient for 100 gpH, initially 8.6; adjusted to6 with lactic acid__________________________________________________________________________
When applied to natural hair, this shampoo composition in the form of a clear liquid, facilitates untangling of wet hair. Dry hair, thus treated, is controlled and shiny.
EXAMPLE 41
The following shampoo composition is prepared:
__________________________________________________________________________RCHOHCH.sub.2O(CH.sub.2CHOHCH.sub.2OH).sub.nwherein R = C.sub.9 to C.sub.12 alkyland n has a statisticalaverage value of 3.5 10 gTriethanolamine C.sub.12 -C.sub.14alkyl sulfate 2 gDiethanolamide of coprafatty acids 3 gCompound of Example Ib 0.5 g active material ##STR29## 0.1 g active materialWater, sufficient for 100 gpH, initially - 7.9; adjustedto 6 with lactic acid__________________________________________________________________________
When applied to dyed hair, this shampoo composition in the form of a slightly opalescent liquid facilitates the untangling of wet hair and imparts softness thereto. Dry hair, thus treated, is lively and full.
EXAMPLE 4m
The following shampoo composition is prepared:
______________________________________C.sub.12 -C.sub.14 alcohol ethoxylatedwith 10 moles of ethyleneoxide and carboxymethylated,sold under the mark"AKYPO RLM 100" 3 gLauryl alcohol polyethoxylatedwith 12 moles ofethylene oxide 7 gLauric diethanolamide 3 gCompound of Example IIIb 0.6 g active material ##STR30## 0.3 g active materialWater, sufficient for 100 gpH, initially - 4.5; adjusted to7.2 with triethanolamine______________________________________
When applied to dyed hair, this shampoo composition in the form of a clear liquid, facilitates the untangling of wet hair. Dry hair, thus treated is shiny.
EXAMPLE 4n
The following shampoo composition is prepared:
__________________________________________________________________________RCHOHCH.sub.2O(CH.sub.2CHOHCH.sub.2OH).sub.nwherein R = C.sub.9 to C.sub.12alkyl and n has a statisticalaverage value of 3.5 10 gDiethanolamide of coprafatty acids 2 gCompound of Example Ib 0.7 g active material ##STR31## 0.3 gWater, sufficient for 100 gpH = 7__________________________________________________________________________
When applied to natural, permanent waved hair, this shampoo composition in the form of a clear liquid, facilitates the untangling of wet hair and imparts softness thereto. Dry hair, thus treated, is lively, full and easyto control.
EXAMPLE 4o
The following shampoo composition is prepared:
______________________________________Triethanolamine C.sub.12 -C.sub.14alkyl sulfate 10 gLauric diethanolamide 2 gHydroxypropylmethyl cellulose 0.2 gCompound of Example Vb 0.8 gPerfume 0.1 gDyes 0.01 gWater, sufficient for 100 gpH, adjusted to 8 withtriethanolamine______________________________________
This clear liquid shampoo composition improves the untangling of wet hair. It imparts to dry hair thus treated good control.
EXAMPLE 4p
The following shampoo composition is prepared:
______________________________________Triethanolamine C.sub.12 -C.sub.14alkyl sulfate 15 gHydroxypropylmethyl cellulose 0.2 gLauric diethanolamide 3 gCompound of Example IXb 1 gPerfume 0.2 gDyes 0.01 gWater, sufficient for 100 gpH = 7.7______________________________________
EXAMPLE 4q
The following shampoo composition is prepared:
______________________________________Triethanolamine C.sub.12 -C.sub.14alkyl sulfate 10 gHydroxypropylmethyl cellulose 0.3 gCompound of Example Xb 1 gPerfume 0.1 gDyes 0.015 gWater, sufficient for 100 gpH = 7.7______________________________________
EXAMPLE 5a
The following "after-shampoo" care cream is prepared:
______________________________________Cetyl alcohol 20 gCetyl alcohol oxyethylenatedwith 10 moles of ethyleneoxide, sold under themark "BR1J 50" 12 g ##STR32## 1.5 g active materialCompound of Example VIIb 0.5 g active materialPhosphoric acid ester ofethoxylated oleyl alcohol,sold under the mark"DIVALIN SO" 1 gWater, sufficient for 100 g______________________________________
EXAMPLE 5b
The following "after-shampoo" care cream is prepared:
______________________________________Cetyl alcohol 22 gCetyl alcohol oxyethylenatedwith 10 moles of ethyleneoxide, sold under the mark"BR1J 56" 10 gCompound of Example IVb 0.5 g active materialPhosphoric acid ester ofethoxylated oleyl alcohol,sold under the mark"DIVALIN SO" 1.2 gWater, sufficient for 100 g______________________________________
The care creams of Examples 5a and 5b are applied to clean, moist or dried hair, in an amount sufficient to impregnate and cover the hair (about 60 to 80 g). The cream is permitted to remain in contact with the hair for 30-40 minutes at which time it is then rinsed off. The wet hair is very soft and easy to comb. The hair is then set and dried under a hood. The dry hair combs easily and has a silky touch; is shiny and lively; has bodyand is full.
EXAMPLE 5c
The following "before shampoo" care cream is prepared:
______________________________________Stearic acid 12 gCetyl-stearyl alcoholoxyethylenated with 10moles of ethylene oxide 4 gMonoethanolamine 2 gGlycerine 4 g ##STR33## 1.2 g active materialCompound of Example VIIIb 0.5 g active materialPerfume and dyesWater, sufficient for 100 gpH, adjusted to 7______________________________________
EXAMPLE 5d
The following "before shampoo" care cream is prepared:
______________________________________Stearic acid 12 gCetyl-stearyl alcoholoxyethylenated with 10moles of ethylene oxide 6 gMonoethanolamine 3 gGlycerine 3 gCompound of Example IIIb 0.8 g active materialPerfume - DyesWater, sufficient for 100 gpH, adjusted to 7______________________________________
The care creams of Example 5c and 5d are applied to soiled, wet hair at a rate of 60 grams. The hair is impregnated therewith by rubbing and the cream is permitted to remain in contact therewith for 30 minutes. The hairis then shampooed. The wet hair is very soft and easy to untangle. After setting and drying, the hair has a particularly soft feel; it is shiny, lively and has body. This effect lasts after several shampooings.
EXAMPLE 6a
The following hair structuring lotion without rinsing is prepared:
______________________________________Dimethylol ethylene thioureaof the formula ##STR34## 0.5 gQuaternary polyvinylpyrrolidonecopolymer, M.W. = about1,000,000, sold under themark "GAFQUAT 755" 0.5 gCompound of Example Ib 0.4 g active materialVinylpyrrolidone-vinyl acetatecopolymer, VP/VA = 70:30 0.8 gPhosphoric acid, sufficient for pH = 3Water, sufficient for 100 cc______________________________________
This lotion is applied to washed and dried hair after a shampoo and before setting. In the wet state the hair untangles easily and has a silky touch.After setting and drying, the hair is shiny and lively.
EXAMPLE 6b
This example is similar to Example 6a except that the compound of Example Ib is replaced by an equal amount of the compound of Example IVb.
EXAMPLE 7a
The following non-rinse lotion for use before a permanent is prepared:
______________________________________Trimethyl cetylammonium bromide 0.1 gCompound of Example IVb 1.5 gPerfume 0.1 gDyes 0.1 gCitric acid, sufficient for pH = 5Water, sufficient for 100 g______________________________________
When applied to washed hair, this non-rinse product facilitates combing andpermits easy implementation of the permanent wave. It protects the hair andprolongs the hold of the waves.
EXAMPLE 7b
The following non-rinse lotion for use before a permanent is prepared:
______________________________________Trimethylcetylammonium bromide 0.15 gCompound of Example VIIb 2.2 gPerfume 0.2 gDyes 0.01 gCitric acid, sufficient for pH = 4Water, sufficient for 100 g______________________________________
When applied to washed hair, this non-rinse product facilitates combing andpermits easy implementation of the permanent. It protects the hair and prolongs the hold of the wave.
EXAMPLE 8a
The following permanent wave composition is prepared:
______________________________________Reducing agent liquidThioglycolic acid 3 gThiolactic acid 2 gAmmonia, 22.degree. Be 4 gTriethanolamine 3.5 gCompound of Example VIb 1.4 gPerfume 0.2 gDyes 0.05 gWater, sufficient for 100 gFixing Agent LiquidPotassium bromate 9.5 gCetylpyridinium chloride 1 gTartaric acid, sufficient for pH = 6.5Perfume 0.1 gDyes 0.05 gWater, sufficient for 100 g______________________________________
On sensitized hair, the reducing agent liquid is applied very easily and itdeeply penetrates the hair. After rinsing and after application of the fixing agent liquid, a very strong and regular wave is attained. The hair is in a very beautiful cosmetic state. After drying, the hair is very softand particularly shiny. The hold of the hair style is particularly good.
EXAMPLE 8b
The following permanent wave composition is prepared:
______________________________________Reducing Agent LiquidThioglycolic acid 3.5 gThiolactic acid 2 gAmmonia, 22.degree. Be 3.5 gTriethanolamine 4 gCompound of Example VIIIb 2 gPerfume 0.2 gDyes 0.01 gWater, sufficient for 100 gFixing Agent LiquidPotassium bromate 8 gCetylpyridinium chloride 0.8 gTartaric acid, sufficient for pH = 6.5Perfume 0.2 gDyes 0.05 gWater, sufficient for 100 g______________________________________
On sensitized hair, the reducing agent liquid is applied easily and it penetrates deeply into the hair. After rinsing and after application of the fixing agent liquid, a very strong and very regular wave is obtained. The hair is in a very beautiful cosmetic state. After drying, the hair is very soft and particularly shiny. The hold of the hair style is particularly good.

Claims

1. A crosslinked polymer, which is soluble in water at 10 weight percent thereof without gel formation, obtained by crosslinking a polyamino-polyamide with a crosslinking agent wherein said crosslinking agent is employed in an amount of 0.025 to 0.35 mole per amine group of said polyamino-polyamide, said polyamino-polyamide being prepared by the polycondensation of (a) an acidic compound selected from the group consisting of (i) an acid selected from the group consistintg of an organic saturated dicarboxylic acid having from 6 to 10 carbon atoms and terephthalic acid, (ii) the addition compound of one mole of an alkylenediamine with two moles of an unsaturated acid selected from the group consisting of acrylic acid, methacrylic acid and itaconic acid, (iii) an ester of said compounds of (i) and (ii) with a lower alkanol having 1-6 carbon atoms and (iv) mixtures of (i), (ii) and (iii) on (b) a polyamine selected from the group consisting of bis-primary mono-secondary polyalkylene polyamine and bis-primary bis-secondary polyalkylene polyamine, said polyamine (b) being replaceable by a member selected from the group consisting of (1) up to 20 mole percent hexamethylene diamine, (2) up to 40 mole percent bis-primary amine and (3) up to 40 mole percent bis-secondary amine, said crosslinking agent being selected from the group consisting of:
(I) simple bi-functional compounds selected from the group consisting of (1) bis-halohydrins resulting from the reaction of an epihalohydrin with a primary amine, a bis-secondary diamine, a bis-phenol or a bis-mercaptan, (2) a bis-azetidinium derived from N,N-dialkyl halogeno hydroxy propylamine by cyclization or from bis-halohydrin for which the halohydrin units are linked to the remainder of the molecule by tertiary nitrogen groups, and carry two azetidinium groups or one azetidinium group and one halohydrin group, (3) a bis-haloacyl diamine, and (4) an alkyl bis-halide of the formula ##STR35## wherein X=Cl or Br, Z represents ##STR36## x=1 to 3, m=0 or 1, n=0 or 1, m and n do not represent 1 at the same time, with the proviso that when m=1, x=1, A.sub.1 represents a saturated divalent hydrocarbon radical having 2,3,4 or 6 carbon atoms or 2-hydroxyl propylene;
(II) an oligomer obtained by the reaction of compound (a) selected from the group consisting of compounds (1), (2), (3) and (4), each defined above, (5) an epihalohydrin, (6) a bis-epoxide and (7) a bis-unsaturated derivative, with a compound (b) which is a bi-functional compound reactive with said compound (a), said compound (b) being selected from the group consisting of primary amine, a bis-secondary diamine, a bis-mercaptan and a bis-phenol, the molar ratio of (b):(a) being between 0.1 and 0.9;
(II-bis) an oligomer obtained by the reaction of compound (a.sub.1) selected from the group consisting of compounds (1), (3), (4) and (6) each defined above, with a bis-tertiary diamine (b.sub.1) which is a bi-functional compound reactive with said compound (a.sub.1), the molar ratio of (b.sub.1):(a.sub.1) being between 0.1 and 0.9;
(III) the quaternization product of compound (a.sub.2) selected from the group consisting of (1) a bis-halohydrin resulting from the reaction of an epihalohydrin with piperizine, a bis-phenol or a bis-mercaptan; (2) a bis-azetidinum, defined above in (I) (2), (3) a bis-haloacyl diamine, (4) an alkyl bis-halide of formula F.sub.1 above, (6) a bis-epoxide, (7) a bis-unsaturated derivative, (8) an oligomer II obtained by the reaction of compound (a.sub.3) selected from the group consisting of compounds (1), (2), (3), (4), (6) and (7) each defined above with a compound (b.sub.3) which is a bi-functional compound reactive with said compound (a.sub.3), said compound (b.sub.3) being selected from the group consisting of a primary amine, a bis-secondary diamine, a bis-mercaptan and a bis-phenol, the molar ratio of (b.sub.3):(a.sub.3) being between 0.1 and 0.9; (9) an oligomer obtained by the reaction of an epihalohydrin (a.sub.4) with a compound (b.sub.4) which is a bi-functional compound reactive with said compound (a.sub.4), said compound (b.sub.4) being selected from the group consisting of piperazine, a bis-mercaptan, a bis-phenol and a bis-epoxide of piperazine, the molar ratio of (b.sub.4):(a.sub.4) being between 0.1 and 0.9, and (10) an oligomer obtained by the reaction of a compound (a.sub.5) selected from the group consisting of (1) a bis-halohydrin resulting from the reaction of an epihalohydrin with piperazine, a bis-phenol or a bis-mercaptan, (2) a bis-halocyl diamine, (3) an alkyl bis-halide of formula F.sub.1 above and (4) a bis-epoxide, with a compound (b.sub.5), said compound (b.sub.5) being a bis-tertiary diamine, the molar ratio (b.sub.5):(a.sub.5) being between 0.1 and 0.9; and
said product having a tertiary amine group alkylated with an alkylating agent (c) selected from the group consisting of methyl or ethyl chloride, bromide, iodide, sulfate, mesylate and tosylate, benzyl chloride or bromide, ethylene oxide, propylene oxide and glycidol.
2. The polymer of claim 1 wherein said acidic compound employed in preparing said polyaminopolyamide is selected from the group consisting of adipic acid, terephthalic acid, the dimethyl ester of said acids and the addition product of ethylenediamine on acrylic acid, methacrylic acid or itaconic acid, or their methyl esters.
3. The polymer of claim 1 wherein the polyamine employed in preparing said polyamino-polyamide is selected from the group consisting of diethylene triamine, dipropylene triamine, triethylene tetramine and a mixture of any one thereof with one or more of ethylene diamine, hexamethylene diamine and piperazine.
4. The polymer of claim 1 wherein said polyaminopolyamide is obtained by the condensation of adipic acid on diethylene triamine.
5. The polymer of claim 1 wherein said crosslinking agent is employed in an amount of 0.025 to about 0.2 mole per amine group of said polyamino-polyamide.
6. The polymer of claim 1 wherein said crosslinking agent is employed in an amount of 0.025 to about 0.1 mole per amine group of said polyamino-polyamide.
7. The polymer of claim 1 wherein said crosslinking agent is selected from the group consisting of
a bis halohydrin selected from the group consisting of ##STR37## (5) X--CH.sub.2 --CHOH--CH.sub.2 O--CH.sub.2 --CH.sub.2 --O--.sub.p CH.sub.2 --CHOH--CH.sub.2 X wherein p=0-25, ##STR38## and (7) X--CH.sub.2 --CHOH--CH.sub.2 --S--(CH.sub.2).sub.q --S--CH.sub.2 --CHOH--CH.sub.2 X, wherein q=2-6, and X in (1)-(7) above represents Cl or Br;
a bis-azetidinium of the formula ##STR39## a bis-haloacyl diamine of the formula (9) ##STR40## wherein X=Cl or Br, A=--CH.sub.2 --CH.sub.2 --, --CH.sub.2 --CH.sub.2 --CH.sub.2 -- or ##STR41## n=1-10, R.sub.1 =R.sub.2 =hydrogen or R.sub.1 and R.sub.2 linked together represent ethylene; when ##STR42## R.sub.1 and R.sub.2 represent hydrogen; when A=--CH.sub.2 --CH.sub.2 --, R.sub.1 and R.sub.2 can be linked together and represent ethylene with the group ##STR43## and an alkyl bis-halide of the formula ##STR44## wherein X=Cl or Br, Z represents ##STR45## x=1-3, m=0 or 1, n=0 or 1, m and n not representing 1 at the same time, when m=1, x=1, and A.sub.1 represents a divalent hydrocarbon radical having 2, 3, 4 or 6 carbon atoms or 2-hydroxy propylene.
8. The polymer of claim 1 wherein the bi-functional reactive compound (b) in crosslinking agent (II) is selected from the group consisting of a primary amine, a bis-secondary diamine and a bis-mercaptan.
9. The polymer of claim 1 wherein the bi-functional reactive compound (b) in crosslinking agent (II) is selected from the group consisting of piperazine and 1,2-dithiol ethane.
10. The polymer of claim 1 wherein compound (a) in crosslinking agent (II) is selected from the group consisting of (1) a bis-halohydrin resulting from the reaction of an epihalohydrin with a primary amine, a bis-secondary diamine, a bis-phenol or a bis-mercaptan, (2) a bis-azetidinium defined in (I)(2), (3) a bis-haloacyl diamine, (4) an alkyl bis-halide of the formula ##STR46## wherein X=Cl or Br, Z represents ##STR47## x=1-3, m=0 or 1, n=0 or 1, m and n not representing 1 at the same time, when m=1, x=1; A.sub.1 represents a saturated divalent hydrocarbon radical having 2, 3, 4 or 6 carbon atoms or 2-hydroxy propylene, (5) an epihalohydrin, and (6) a bis-epoxide and
the compound (b) is a bis-phenol.
11. The polymer of claim 10 wherein compound (b) is bis-phenol A or 2,2-(4,4'-dihydroxy diphenyl) propane.
12. The polymer of claim 1 wherein the bifunctional reactive compound (b.sub.1) in crosslinking agent (II-bis) is a bis-tertiary diamine.
13. The polymer of claim 12 wherein compound (b.sub.1) is selected from the group consisting of N,N,N',N'-tetramethyl ethylene-, propylene-, butylene- or hexamethylene-diamine.
14. The polymer of claim 1 wherein the alkylating agent (c) is dimethyl sulfate.
15. The polymer of claim 1 wherein said bisazetidinium is derived from a bis-halohydrin wherein the halohydrin units are linked to the remainder of the molecule by tertiary nitrogen groups, said bis-azetidinium carrying two azetidinium groups or one azetidinium group and one halohydrin group.
16. The polymer of claim 1 wherein said crosslinking agent is selected from the group consisting of ##STR48##
17. The crosslinked polymer of claim 1 wherein up to 20 mole percent of said polyamine (b) is replaced by hexamethylene diamine.
18. The crosslinked polymer of claim 1 wherein up to 40 mole percent of said polyamine (b) is replaced by a ethylene diamine.
19. The crosslinked polymer of claim 1 wherein up to 40 mole percent of said polyamine (b) is replaced by piperazine.
20. A crosslinked polymer which is soluble in water at 10 weight percent thereof without gel formation, obtained by crosslinking a polyamino-polyamide with a crosslinking agent wherein said crosslinking agent is employed in an amount of 0.025 to 0.35 mole per amine group of said polyamino-polyamide, said polyamino-polyamide being prepared by the polycondensation of adipic acid on diethylene triamine,
said crosslinking agent being selected from the group consisting of: ##STR49##
21. A crosslinked polymer which is soluble in water at 10 percent thereof without gel formation, obtained by crosslinking a polyamino-polyamide with a crosslinking agent wherein said crosslinking agent is employed in an amount of 0.025 to 0.35 mole per amine group of said polyamino-polyamide, said polyamino-polyamide being prepared by the polycondensation of an acidic compound selected from the group consisting of adipic acid, terephthalic acid, the dimethyl ester of said acids and the addition product of one mole of ethylenediamine on two moles of acrylic acid, methacrylic acid or itaconic acid, or their methyl esters, on a polyamine selected from the group consisting of (i) diethylene triamine, (ii) dipropylene triamine, (iii) triethylene tetraamine and a mixture of any one of (i), (ii) and (iii) with one or more of ethylene diamine, hexamethylene diamine and piperazine,
said crosslinking agent being selected from the group consisting of: ##STR50##
22. A crosslinked polymer, which is soluble in water at 10 weight percent thereof without gel formation, obtained by crosslinking a polyamino-polyamide with a crosslinking agent wherein said crosslinking agent is employed in an amount of 0.025 to 0.35 mole per amine group of said polyamino-polyamide, said polyamino-polyamide being prepared by the polycondensation of (a) an acidic compound selected from the group consisting of (i) an acid selected from the group consisting of an organic saturated dicarboxylic acid having from 6 to 10 carbon atoms and terephthalic acid, (ii) the addition compound of one mole of an alkylenediamine with two moles of an unsaturated acid selected from the group consisting of acrylic acid, methacrylic acid and itaconic acid, (iii) an ester of said compounds of (i) and (ii) with a lower alkanol having 1-6 carbon atoms and (iv) mixtures of (i), (ii) and (iii) on (b) a polyamine selected from the group consisting of a bis-primary mono-secondary polyalkylene polyamine and a bis-primary bis-secondary polyalkylene polyamine, said polyamine (b) being replaceable by a member selected from the group consisting of (1) up to 20 mole percent hexamethylene diamine, (2) up to 40 mole percent bis-primary amine and (3) up to 40 mole percent bis-secondary amine, said crosslinking agent being a bis-halohydrin having the formula ##STR51## wherein n is 1-4 and X is Cl or Br.
23. A crosslinked polymer, which is soluble in water at 10 weight percent thereof without gel formation, obtained by crosslinking a polyamino-polyamide with a crosslinking agent wherein said crosslinking agent is employed in an amount of 0.025 to 0.35 mole per amine group of said polyamino-polyamide, said polyamino-polyamide being prepared by the polycondensation of (a) an acidic compound selected from the group consisting of (i) an acid selected from the group consisting of an organic saturated dicarboxylic acid having from 6 to 10 carbon atoms and terephthalic acid, (ii) the addition compound of one mole of an alkylenediamine with two moles of an unsaturated acid selected from the group consisting of acrylic acid, methacrylic acid and itaconic acid, (iii) an ester of said compounds of (i) and (ii) with a lower alkanol having 1-6 carbon atoms and (iv) mixtures of (i), (ii) and (iii) on (b) a polyamine selected from the group consisting of a bis-primary mono-secondary polyalkylene polyamine and a bis-primary bis-secondary polyalkylene polyamine, said polyamine (b) being replaceable by a member selected from the group consisting of (1) up to 20 mole percent hexamethylene diamine, (2) up to 40 mole percent bis-primary amine and (3) up to 40 mole percent bis-secondary amine, said crosslinking agent being a bis-halohydrin having the formula ##STR52## wherein X is Cl or Br.
24. A crosslinked polymer, which is soluble in water at 10 weight percent thereof without gel formation, obtained by crosslinking a polyamino-polyamide with a crosslinking agent wherein said crosslinking agent is employed in an amount of 0.025 to 0.35 mole per amine group of said polyamino-polyamide, said polyamino-polyamide being prepared by the polycondensation of (a) an acidic compound selected from the group consisting of (i) an acid selected from the group consisting of an organic saturated dicarboxylic acid having from 6 to 10 carbon atoms and terephthalic acid, (ii) the addition compound of one mole of an alkylenediamine with two moles of an unsaturated acid selected from the group consisting of acrylic acid, methacrylic acid and itaconic acid, (iii) an ester of said compounds of (i) and (ii) with a lower alkanol having 1-6 carbon atoms and (iv) mixtures of (i), (ii) and (iii) on (b) a polyamine selected from the group consisting of a bis-primary mono-secondary polyalkylene polyamine and a bis-primary bis-secondary polyalkylene polyamine, said polyamine (b) being replaceable by a member selected from the group consisting of (1) up to 20 mole percent hexamethylene diamine, (2) up to 40 mole percent bis-primary amine and (3) up to 40 mole percent bis-secondary amine, said crosslinking agent being a bis-halohydrin having the formula ##STR53## wherein n is 2-6 and X is Cl or Br.
25. A crosslinked polymer, which is soluble in water at 10 weight percent thereof without gel formation, obtained by crosslinking a polyamino-polyamide with a crosslinking agent wherein said crosslinking agent is employed in an amount of 0.025 to 0.35 mole per amine group of said polyamino-polyamide, said polyamino-polyamide being prepared by the polycondensation of (a) an acidic compound selected from the group consisting of (i) an acid selected from the group consisting of an organic saturated dicarboxylic acid having from 6 to 10 carbon atoms and terephthalic acid, (ii) the addition compound of one mole of an alkylenediamine with two moles of an unsaturated acid selected from the group consisting of acrylic acid, methacrylic acid and itaconic acid, (iii) an ester of said compounds of (i) and (ii) with a lower alkanol having 1-6 carbon atoms and (iv) mixtures of (i), (ii) and (iii) on (b) a polyamine selected from the group consisting of a bis-primary mono-secondary polyalkylene polyamine and a bis-primary bis-secondary polyalkylene polyamine, said polyamine (b) being replaceable by a member selected from the group consisting of (1) up to 20 mole percent hexamethylene diamine, (2) up to 40 mole percent bis-primary amine and (3) up to 40 mole percent bis-secondary amine, said crosslinking agent being a bis-halohydrin having the formula ##STR54## wherein R=C.sub.n H.sub.2n+1 wherein n=1-18 or --(CH.sub.2 --CH.sub.2 --O--.sub.m H wherein m is 1 or 2 and X is Cl or Br.
26. A crosslinked polymer, which is soluble in water at 10 weight percent thereof without gel formation, obtained by crosslinking a polyamino-polyamide with a crosslinking agent wherein said crosslinking agent is employed in an amount of 0.025 to 0.35 mole per amine group of said polyamino-polyamide, said polyamino-polyamide being prepared by the polycondensation of (a) an acidic compound selected from the group consisting of (i) an acid selected from the group consisting of an organic saturated dicarboxylic acid having from 6 to 10 carbon atoms and terephthalic acid, (ii) the addition compound of one mole of an alkylenediamine with two moles of an unsaturated acid selected from the group consisting of acrylic acid, methacrylic acid and itaconic acid, (iii) an ester of said compounds of (i) and (ii) with a lower alkanol having 1-6 carbon atoms and (iv) mixtures of (i), (ii) and (iii) on (b) a polyamine selected from the group consisting of a bis-primary mono-secondary polyalkylene polyamine and a bis-primary bis-secondary polyalkylene polyamine, said polyamine (b) being replaceable by a member selected from the group consisting of (1) up to 20 mole percent hexamethylene diamine, (2) up to 40 mole percent bis-primary amine and (3) up to 40 mole percent bis-secondary amine, said crosslinking agent being a bis halohydrin having the formula
X--CH.sub.2 --CHOH--CH.sub.2 --O--CH.sub.2 --CH.sub.2 --O--.sub.p CH.sub.2 --CHOH--CH.sub.2 X
wherein p is 0-25 and X is Cl or Br.
27. A crosslinked polymer, which is soluble in water at 10 weight percent thereof without gel formation, obtained by crosslinking a polyamino-polyamide with a crosslinking agent wherein said crosslinking agent is employed in an amount of 0.025 to 0.35 mole per amine group of said polyamino-polyamide, said polyamino-polyamide being prepared by the polycondensation of (a) an acidic compound selected from the group consisting of (i) an acid selected from the group consisting of an organic saturated dicarboxylic acid having from 6 to 10 carbon atoms and terephthalic acid, (ii) the addition compound of one mole of an alkylenediamine with two moles of an unsaturated acid selected from the group consisting of acrylic acid, methacrylic acid and itaconic acid, (iii) an ester of said compounds of (i) and (ii) with a lower alkanol having 1-6 carbon atoms and (iv) mixtures of (i), (ii) and (iii) on (b) a polyamine selected from the group consisting of a bis-primary mono-secondary polyalkylene polyamine and a bis-primary bis-secondary polyalkylene polyamine, said polyamine (b) being replaceable by a member selected from the group consisting of (1) up to 20 mole percent hexamethylene diamine, (2) up to 40 mole percent bis-primary amine and (3) up to 40 mole percent bis-secondary amine, said crosslinking agent being a bis-halohydrin having the formula ##STR55## wherein X is Cl or Br.
28. A crosslinked polymer, which is soluble in water at 10 weight percent thereof without gel formation, obtained by crosslinking a polyamino-polyamide with a crosslinking agent wherein said crosslinking agent is employed in an amount of 0.025 to 0.35 mole per amine group of said polyamino-polyamide, said polyamino-polyamide being prepared by the polycondensation of (a) an acidic compound selected from the group consisting of (i) an acid selected from the group consisting of an organic saturated dicarboxylic acid having from 6 to 10 carbon atoms and terephthalic acid, (ii) the addition compound of one mole of an alkylenediamine with two moles of an unsaturated acid selected from the group consisting of acrylic acid, methacrylic acid and itaconic acid, (iii) an ester of said compounds of (i) and (ii) with a lower alkanol having 1-6 carbon atoms and (iv) mixtures of (i), (ii) and (iii) on (b) a polyamine selected from the group consisting of a bis-primary mono-secondary polyalkylene polyamine and a bis-primary bis-secondary polyalkylene polyamine, said polyamine (b) being replaceable by a member selected from the group consisting of (1) up to 20 mole percent hexamethylene diamine, (2) up to 40 mole percent bis-primary amine and (3) up to 40 mole percent bis-secondary amine, said crosslinking agnet being a bis-halohydrin having the formula
X--CH.sub.2 --CHOH--CH.sub.2 --S--(CH.sub.2).sub.q --S--CH.sub.2 --CHOH--CH.sub.2 X
wherein q is 2-6 and X is Cl or Br.
29. A crosslinked polymer, which is soluble in water at 10 weight percent thereof without gel formation, obtained by crosslinking a polyamino-polyamide with a crosslinking agent wherein said crosslinking agent is employed in an amount of 0.025 to 0.35 mole per amine group of said polyamino-polyamide, said polyamino-polyamide being prepared by the polycondensation of (a) an acidic compound selected from the group consisting of (i) an acid selected from the group consisting of an organic saturated dicarboxylic acid having from 6 to 10 carbon atoms and terephthalic acid, (ii) the addition compound of one mole of an alkylenediamine with two moles of an unsaturated acid selected from the group consisting of acrylic acid, methacrylic acid and itaconic acid, (iii) an ester of said compounds of (i) and (ii) with a lower alkanol having 1-6 carbon atoms and (iv) mixtures of (i), (ii) and (iii) on (b) a polyamine selected from the group consisting of a bis-primary mono-secondary polyalkylene polyamine and a bis-primary bis-secondary polyalkylene polyamine, said polyamine (b) being replaceable by a member selected from the group consisting of (1) up to 20 mole percent hexamethylene diamine, (2) up to 40 mole percent bis-primary amine and (3) up to 40 mole percent bis-secondary amine, said crosslinking agent being a bis-azetidinium of the formula ##STR56##
30. A crosslinked polymer, which is soluble in water at 10 weight percent thereof without gel formation, obtained by crosslinking a polyamino-polyamide with a crosslinking agent wherein said crosslinking agent is employed in an amount of 0.025 to 0.35 mole per amine group of said polyamino-polyamide, said polyamino-polyamide being prepared by the polycondensation of (a) an acidic compound selected from the group consisting of (i) an acid selected from the group consisting of an organic saturated dicarboxylic acid having from 6 to 10 carbon atoms and terephthalic acid, (ii) the addition compound of one mole of an alkylenediamine with two moles of an unsaturated acid selected from the group consisting of acrylic acid, methacrylic acid and itaconic acid, (iii) an ester of said compounds of (i) and (ii) with a lower alkanol having 1-6 carbon atoms and (iv) mixtures of (i), (ii) and (iii) on (b) a polyamine selected from the group consisting of a bis-primary mono-secondary polyalkylene polyamine and a bis-primary bis-secondary polyalkylene polyamine, said polyamine (b) being replaceable by a member selected from the group consisting of (1) up to 20 mole percent hexamethylene diamine, (2) up to 40 mole percent bis-primary amine and (3) up to 40 mole percent bis-secondary amine, said crosslinking agent being a bis-haloacyl diamine of the formula ##STR57## wherein X is Cl or Br, A is --CH.sub.2 --CH.sub.2 --, --CH.sub.2 --CH.sub.2 --CH.sub.2 -- or ##STR58## n=1-10, R.sub.1 =R.sub.2 =hydrogen or R.sub.1 and R.sub.2 linked together represent ethylene; when ##STR59## R.sub.1 and R.sub.2 represent hydrogen; when A=--CH.sub.2 --CH.sub.2 --, R.sub.1 and R.sub.2 can be linked together and represent ethylene with the group ##STR60##
31. A crosslinked polymer, which is soluble in water at 10 weight percent thereof without gel formation, obtained by crosslinking a polyamino-polyamine with a crosslinking agent wherein said crosslinking agent is employed in an amount of 0.025 to 0.35 mole per amine group of said polyamino-polyamide, said polyamino-polyamide being prepared by the polycondensation of (a) an acidic compound selected from the group consisting of (i) an acid selected from the group consisting of an organic saturated dicarboxylic acid having from 6 to 10 carbon atoms and terephthalic acid, (ii) the addition compound of one mole of an alkylenediamine with two moles of an unsaturated acid selected from the group consisting of acrylic acid, methacrylic acid and itaconic acid, (iii) an ester of said compounds of (i) and (ii) with a lower alkanol having 1-6 carbon atoms and (iv) mixtures of (i), (ii) and (iii) on (b) a polyamine selected from the group consisting of bis-primary mono-secondary polyalkylene polyamine and bis-primary bis-secondary polyalkylene polyamine, said polyamine (b) being replaceable by a member selected from the group consisting of (1) up to 20 mole percent hexamethylene diamine, (2) up to 40 mole percent bis-primary amine and (3) up to 40 mole percent bis-secondary amine, said crosslinking agent being an alkyl bis-halide of the formula ##STR61## wherein X=Cl or Br, Z represents ##STR62## x=1-3, m=0 or 1, n=0 or 1, m and n not representing 1 at the same time, when m=1, x=1, and A.sub.1 represents a divalent hydrocarbon radical having 2, 3, 4 or 6 carbon atoms or 2-hydroxy propylene.
32. A crosslinked polymer obtained by crosslinking a polyamino-polyamide with a crosslinking agent, said polyamino-polyamide being prepared by the polycondensation of equimolar amounts of adipic acid and diethylene triamine, said polyamino-polyamide characterized by the following unit
--OC-(CH.sub.2).sub.4 --CONH--(CH.sub.2 --CH.sub.2 --NH.sub.2).sub.2 --
and said crosslinking agent being obtained by the reaction of piperazine bis-acrylamide and piperazine in molar proportions of 3/2 and having the formula ##STR63##
33. A crosslinked polymer obtained by crosslinking a polyamino-polyamide with a crosslinking agent, said polyamino-polyamide being prepared by the polycondensation of equimolar amounts of adipic acid and diethylene triamine, said polyamino-polyamide characterized by the following unit
--OC--(CH.sub.2).sub.4 --CONH--(CH.sub.2 --CH.sub.2 --NH.sub.2).sub.2 --
and said crosslinking agent being obtained by the reaction of epichlorohydrin and piperazine in molar proportions of 5/4 and having the formula ##STR64## where n=4.
34. A crosslinked polymer obtained by crosslinking a polyamino-polyamide with a crosslinking agent, said polyamino-polyamide being prepared by the polycondensation of equimolar amounts of adipic acid and diethylene triamine, said polyamino-polyamide characterized by the following unit
--OC--(CH.sub.2).sub.4 --CONH--(CH.sub.2 --CH.sub.2 --NH.sub.2).sub.2 --
and said crosslinking agent having the formula ##STR65##
35. A crosslinked polymer obtained by crosslinking a polyamino-polyamide with a crosslinking agent, said polyamino-polyamide being prepared by the polycondensation of equimolar amounts of adipic acid and diethylene triamine, said polyamino-polyamide characterized by the following unit
--OC--(CH.sub.2).sub.4 --CONH--(CH.sub.2 --CH.sub.2 --NH.sub.2).sub.2 --
and said crosslinking agent having the formula ##STR66##
36. A crosslinked polymer obtained by crosslinking a polyamino-polyamide with a crosslinking agent, said polyamino-polyamide being prepared by the polycondensation of equimolar amounts of adipic acid and diethylene triamine, said polyamino-polyamide characterized by the following unit
--OC--(CH.sub.2).sub.4 --CONH--(CH.sub.2 --CH.sub.2 --NH.sub.2).sub.2 --
and said crosslinking agent having the formula ##STR67##
37. A crosslinked polymer obtained by crosslinking a polyamino-polyamide with a crosslinking agent, said polyamino-polyamide with a crosslinking agent, said polyamino-polyamide being prepared by the polycondensation of equimolar amounts of adipic acid and diethylene triamine, said polyamino-polyamide characterized by the following unit
--OC--(CH.sub.2).sub.4 --CONH--(CH.sub.2 --CH.sub.2 --NH.sub.2).sub.2 --
and
said crosslinking agent being obtained by the reaction of epichlorohydrin and piperazine in molar proportions of 4/3 and having the formula ##STR68##
38. A crosslinked polymer obtained by crosslinking a polyamino-polyamide with a crosslinking agent, said polyamino-polyamide being prepared by the polycondensation of equimolar amounts of adipic acid and diethylene triamine, said polyamino-polyamide characterized by the following unit --OC--(CH.sub.2).sub.4 --CONH--(CH.sub.2 --CH.sub.2 --NH.sub.2).sub.2 -- and said crosslinking agent being obtained by the reaction of epichlorohydrin and piperazine in molar proportions of 3/2 and having the formula ##STR69##

Priority Claims (2)

Number	Date	Country	Kind
68901	Nov 1973	LUX
77 06031	Mar 1977	FRX

Parent Case Info

This application is a division of our application Ser. No. 881,513, filed Feb. 2, 1978, now U.S. Pat. No. 4,189,468, which is a continuation-in-part of application Ser. No. 762,804, filed Jan. 26, 1977, now U.S. Pat. No. 4,172,887, which is a continuation of application Ser. No. 528,577, filed Nov. 29, 1974, now abandoned.

US Referenced Citations (9)

Number	Name	Date
2882185	Valko et al.	Apr 1959
2926116	Keim	Feb 1960
2926154	Keim	Feb 1960
3397161	Miller	Aug 1968
3560609	Korden	Feb 1971
3560610	Korden	Feb 1971
3632559	Matter et al.	Jan 1972
3769398	Hewitt	Oct 1973
3919142	Asai et al.	Nov 1975

Foreign Referenced Citations (6)

Number	Date	Country
2617528	Dec 1976	DEX
1583363	Sep 1969	FRX
2249104	May 1975	FRX
1213745	Nov 1970	GBX
1269381	Apr 1972	GBX
1294514	Nov 1972	GBX

Divisions (1)

	Number	Date	Country
Parent	881513	Feb 1978

Continuations (1)

	Number	Date	Country
Parent	528577	Nov 1974

Continuation in Parts (1)

	Number	Date	Country
Parent	762804	Jan 1977

Polyamino-polyamide crosslinked with crosslinking agent

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Abstract