Patent US4842851A successfully refreshed from Google Patents.
← Back to Patent Explorer
US4842851A Expired / Lapsed US ⏱️ 0.0 years remaining

Polyamino amides for protecting hair against atmospheric attack, and in particular against light, and process for protecting hair employing such polyaminoamides

Assignee: L'Oréal SA
•
Filing: 1987-06-02
•
Granted: 1989-06-27
•
Expires: 2007-06-02
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract The invention relates to the finding that various polyaminoamide polymers function to protect the hair from deterioration due to atmospheric attack, particularly by light, thereby preserving the mechanical properties of the hair. The polyaminoamide polymers are known and include those polyaminoamide polymers described in U.S. Pat. Nos. 2,961,347, 3,227,615, 4,172,887, 4,189,468 and 4,277,581 and French Pat. No. 1,583,363.

Inventors

  • 👤 Jean F. Grollier
  • 👤 Claude Dubief

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-24 16:32
CPC Classifications
A; A61; A61K; A61K8/00; A61K8/18; A61K8/72; A61K8/84; A61K8/88; A61Q; A61Q17/00; A61Q17/04; A61Q5/00; A61Q5/02; A61Q5/06; Y; Y10; Y10S; Y10S424/00; Y10S424/02

Claims Analysis

Total Claims: 15
Claim 1
Independent Claim 670 words
A process for protecting hair keratin against light comprising applying to hair an effective quantity to protect said hair keratin against light of a cosmetic composition containing, in a cosmetically acceptable medium, at least one polyaminoamide selected from the group consisting of (I) a polyaminoamide (A) prepared by polycondensation of an acidic compound selected from the group consisting of (a) an organic dicarboxylic acid, (b) a double bonded aliphatic mono- or dicarboxylic acid, (c) an ester of the acid defined in (a) and (b), and (d) a mixture of the compounds defined in (a), (b) and (c), with a polyamine chosen from a mono- or bis-secondary bis-primary polyalkylenepolyamine, it being possible for 0 to 40 mol % of said polyalkylene polyamine being replaceable by a bis-primary amine or by a bis-secondary amine and it further being possible for 0 to 20 mol % of said polyalkylene polyamine being replaceable by hexamethylenediamine; (II) said polyaminoamide (A) of (I) crosslinked with a crosslinking agent selected from the group consisting of an epihalohydrin, a diepoxide, a dianhydride, an unsaturated anhydride and a bis-unsaturated derivative, said crosslinking agent being employed in an amount of 0.025 to 0.35 mole of crosslinking agent per secondary amine group of said polyaminoamide (A); (III) said crosslinked polyaminoamide (A) of (II) alkylated with an epoxide or an unsaturated derivative; (IV) a water-soluble crosslinked polyaminoamide obtained by crosslinking said polyaminoamide (A) defined in I above, with a crosslinking agent selected from the group consisting of: (1) a simple difunctional compound selected from the group consisting of (a) bishalohydrin, (b) a bisazetidinium, (c) a bishaloacyldiamine and (d) an alkyl bishalide; (2) an oligomer obtained by reaction of a compound (a) selected from the group consisting of (i) a bishalohydrin, (ii) a bisazetidinium, (iii) a bishaloacyldiamine, (iv) an alkyl bishalide, (v) an epihalohydrin, (vi) a diepoxide and (vii) a bis-unsaturated derivative with a compound (b) which is a difunctional compound reactive towards said compound (a); (3) the quaternization product of a compound selected from the group consisting of said compound (1) and said oligomer (2) and containing one or more tertiary amine groups capable of being completely or partially alkylated with an alkylating agent (c) selected from the group consisting of methyl or ethyl chloride, bromide, iodide, sulphate, mesylate and tosylate, benzyl chloride or bromide, ethylene oxide, propylene oxide and glycidol; the crosslinking being carried out by means of 0.025 and 0.35 mole of crosslinking agent per amine group of said polyaminoamide; (V) a water-soluble polyaminoamide derivative resulting from the condensation of a polyalkylene polyamine containing two primary amino groups, at least one secondary amino group and alkylene groups containing 2 to 4 carbon atoms with a dicarboxylic acid having the formula: HOOC--C.sub.m H.sub.2m --COOH in which m denotes an integer from 4 to 8, or with a functional derivative of said dicarboxylic acid, in a molar ratio of 0.8:1 to 1.2:1, followed by an alkylation in aqueous solution with a difunctional agent having the formula ##STR3## in which x denotes an integer from 0 to 7, Z denotes one of ##STR4## R 1 and R 2 each denote a lower alkyl group or a lower hydroxyalkyl group containing 1 to 4 carbon atoms, Y denotes an alkylene radical containing from 2 to 6 carbon atoms, a 2-hydroxy-1,3-propylene radical or one of --CH.sub.2 --CH.sub.2 --NH--CO--NH--CH.sub.2 --CH.sub.2 --and --CH.sub.2 --Ch.sub.2 --CH.sub.2 --NH--CO--NH--CH.sub.2 --CH.sub.2 --CH.sub.2 --, Q.sup.⊖ denotes halogen, sulphate or methosulphate, the quantity of said difunctional alkylating agent being chosen so that the alkylation product remains in solution; and (VI) a water-soluble polymer obtained by reaction of a polyalkylenepolyamine containing two primary amine groups and at least one secondary amine group with a dicarboxylic acid selected from diglycolic acid and a saturated aliphatic dicarboxylic acid containing 3 to 8 carbon atoms; the molar ratio of said polyalkylenepolyamine to said dicarboxylic acid being between 0.8:1 and 1.4:1; the resultant polyamide being reacted with epichlorohydrin in a molar ratio of epichlorohydrin to the secondary amine group of the said polyamide of between 0.5:1 and 1.8:1.
Claim 2
Dependent Claim 670 words
A process for protecting hair keratin against light comprising applying to hair an effective quantity to protect said hair keratin against light of a cosmetic composition containing, in a cosmetically acceptable medium, at least one polyaminoamide selected from the group consisting of (I) a polyaminoamide (A) prepared by polycondensation of an acidic compound selected from the group consisting of (a) an organic dicarboxylic acid, (b) a double bonded aliphatic mono- or dicarboxylic acid, (c) an ester of the acid defined in (a) and (b), and (d) a mixture of the compounds defined in (a), (b) and (c), with a polyamine chosen from a mono- or bis-secondary bis-primary polyalkylenepolyamine, it being possible for 0 to 40 mol % of said polyalkylene polyamine being replaceable by a bis-primary amine or by a bis-secondary amine and it further being possible for 0 to 20 mol % of said polyalkylene polyamine being replaceable by hexamethylenediamine; (II) said polyaminoamide (A) of (I) crosslinked with a crosslinking agent selected from the group consisting of an epihalohydrin, a diepoxide, a dianhydride, an unsaturated anhydride and a bis-unsaturated derivative, said crosslinking agent being employed in an amount of 0.025 to 0.35 mole of crosslinking agent per secondary amine group of said polyaminoamide (A); (III) said crosslinked polyaminoamide (A) of (II) alkylated with an epoxide or an unsaturated derivative; (IV) a water-soluble crosslinked polyaminoamide obtained by crosslinking said polyaminoamide (A) defined in I above, with a crosslinking agent selected from the group consisting of: (1) a simple difunctional compound selected from the group consisting of (a) bishalohydrin, (b) a bisazetidinium, (c) a bishaloacyldiamine and (d) an alkyl bishalide; (2) an oligomer obtained by reaction of a compound (a) selected from the group consisting of (i) a bishalohydrin, (ii) a bisazetidinium, (iii) a bishaloacyldiamine, (iv) an alkyl bishalide, (v) an epihalohydrin, (vi) a diepoxide and (vii) a bis-unsaturated derivative with a compound (b) which is a difunctional compound reactive towards said compound (a); (3) the quaternization product of a compound selected from the group consisting of said compound (1) and said oligomer (2) and containing one or more tertiary amine groups capable of being completely or partially alkylated with an alkylating agent (c) selected from the group consisting of methyl or ethyl chloride, bromide, iodide, sulphate, mesylate and tosylate, benzyl chloride or bromide, ethylene oxide, propylene oxide and glycidol; the crosslinking being carried out by means of 0.025 and 0.35 mole of crosslinking agent per amine group of said polyaminoamide; (V) a water-soluble polyaminoamide derivative resulting from the condensation of a polyalkylene polyamine containing two primary amino groups, at least one secondary amino group and alkylene groups containing 2 to 4 carbon atoms with a dicarboxylic acid having the formula: HOOC--C.sub.m H.sub.2m --COOH in which m denotes an integer from 4 to 8, or with a functional derivative of said dicarboxylic acid, in a molar ratio of 0.8:1 to 1.2:1, followed by an alkylation in aqueous solution with a difunctional agent having the formula ##STR3## in which x denotes an integer from 0 to 7, Z denotes one of ##STR4## R 1 and R 2 each denote a lower alkyl group or a lower hydroxyalkyl group containing 1 to 4 carbon atoms, Y denotes an alkylene radical containing from 2 to 6 carbon atoms, a 2-hydroxy-1,3-propylene radical or one of --CH.sub.2 --CH.sub.2 --NH--CO--NH--CH.sub.2 --CH.sub.2 --and --CH.sub.2 --Ch.sub.2 --CH.sub.2 --NH--CO--NH--CH.sub.2 --CH.sub.2 --CH.sub.2 --, Q.sup.⊖ denotes halogen, sulphate or methosulphate, the quantity of said difunctional alkylating agent being chosen so that the alkylation product remains in solution; and (VI) a water-soluble polymer obtained by reaction of a polyalkylenepolyamine containing two primary amine groups and at least one secondary amine group with a dicarboxylic acid selected from diglycolic acid and a saturated aliphatic dicarboxylic acid containing 3 to 8 carbon atoms; the molar ratio of said polyalkylenepolyamine to said dicarboxylic acid being between 0.8:1 and 1.4:1; the resultant polyamide being reacted with epichlorohydrin in a molar ratio of epichlorohydrin to the secondary amine group of the said polyamide of between 0.5:1 and 1.8:1.
Claim 3
Dependent Claim 36 words
The process of claim 1 wherein said polyaminoamide is a polycondensate of adipic acid with diethylenetriamine, crosslinked with epichlorohydrin in a proportion of 11 moles of epichlorohydrin per 100 secondary amine groups of the said polyaminoamide.
Claim 4
Dependent Claim 42 words
The process of claim 1 wherein said polyaminoamide is a polycondensate of adipic acid with diethylenetriamine, crosslinked with epichlorohydrin in a proportion of 11 moles of epichlorohydrin per hundred secondary amine groups of said polyaminoamide and alkylated by means of trimethylepoxypropylammonium chloride.
Claim 5
Dependent Claim 25 words
The process of claim 1 wherein said polyaminoamide is an adipic acid-dialkylaminohydroxyalkyl-dialkylenetriamine polymer in which the alkyl radical contains from 1 to 4 carbon atoms.
Claim 6
Dependent Claim 24 words
The process of claim 1 wherein said polyaminoamide is a copolymer of adipic acid with diethylenetriamine, crosslinked with epichlorohydrin, or an adipic acid-epoxypropyl-diethylene-triamine copolymer.
Claim 7
Dependent Claim 35 words
The process of claim 1 wherein said cosmetic composition is provided in the form of an aqueous or aqueous-alcoholic solution or dispersion, an oily composition, a cream, a gel, an aerosol foam or a spray.
Claim 8
Dependent Claim 66 words
The process of claim 1 wherein said cosmetic composition additionally contains at least one adjuvant selected from the group consisting of a surface-active agent, a thickener, a polymer other than said polyaminoamide, a softener, a preservative, a foam stabilizer, an electrolyte, an organic solvent, a silicone derivative, an oil, a wax, an antigrease agent, a pH control agent, a colorant, a perfume and a sequestering agent.
Claim 9
Dependent Claim 54 words
The process of claim 1, wherein said cosmetic composition is in the form of a shampoo and contains, in addition to said polyaminoamide, in an aqueous or oily medium, an anionic, cationic, nonionic or amphoteric surface-active agent or a mixture of said surface-active agents, in an amount ranging from 2 and 50 weight percent.
Claim 10
Dependent Claim 70 words
The process of claim 1 wherein said cosmetic composition is in the form of a non-rinsed lotion, gel, cream, spray or foam, said cosmetic composition containing, in an aqueous or aqueous-alcoholic medium, in addition to said polyaminoamide present in an amount ranging from 0.1 to 5 weight percent, a cationic, anionic, nonionic or amphoteric polymer or a mixture thereof, present in an amount ranging from 0.1 to 10 weight percent.
Claim 11
Dependent Claim 63 words
The process of claim 1 wherein said cosmetic composition is in the form of a rinse lotion, emulsion, gel, foam or spray, containing in an aqueous or aqueous-alcoholic medium, in addition to said polyaminoamide present in an amount ranging from 0.1 to 8 weight percent, a nonionic, cationic, anionic or amphoteric polymer present in an amount ranging from 0.1 to 10 weight percent.
Claim 12
Dependent Claim 37 words
The process of claim 1, wherein said cosmetic composition, in the form of a gel, contains in addition to said polyaminoamide, 0.1 to 30 weight percent of a thickener, in the present or not of a solvent.
Claim 13
Dependent Claim 18 words
The process of claim 1 wherein said cosmetic composition contains 0.1 to 8 weight percent of said polyaminoamide.
Claim 14
Dependent Claim 18 words
The process of claim 1 wherein said cosmetic composition contains 0.2 to 3.5 weight percent of said polyaminoamide.
Claim 15
Dependent Claim 18 words
The process of claim 1 wherein said polyaminoamide is a polymer of adipic acid and dimethylaminohydroxypropyl diethylene triamine.

References Cited (Backward Citations)

US2961347A Cited
US3227615A Cited
FR1519979A Cited
FR1527085A Cited
US3632559A Cited
FR2091516A5 Cited
US3821372A Cited
FR2252840A1 Cited
US4172887A Cited
US4189468A Cited
US4277581A Cited
GB2113245A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1992-06-26 1992-12-26 1993-06-27 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1996-06-26 1996-12-26 1997-06-27 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2000-06-26 2000-12-26 2001-06-27 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag