FR2998786A1 - Kit, useful for making-up/caring for nails, includes composition of alkyl cyanoacrylate and polymer including (alkyl)acrylic polymers/copolymers, and another composition of polymer including nucleophilic functions and volatile solvent - Google Patents
Kit, useful for making-up/caring for nails, includes composition of alkyl cyanoacrylate and polymer including (alkyl)acrylic polymers/copolymers, and another composition of polymer including nucleophilic functions and volatile solvent Download PDFInfo
- Publication number
- FR2998786A1 FR2998786A1 FR1261665A FR1261665A FR2998786A1 FR 2998786 A1 FR2998786 A1 FR 2998786A1 FR 1261665 A FR1261665 A FR 1261665A FR 1261665 A FR1261665 A FR 1261665A FR 2998786 A1 FR2998786 A1 FR 2998786A1
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- France
- Prior art keywords
- composition
- nail
- kit according
- polymer
- nails
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 116
- 229920000642 polymer Polymers 0.000 title claims abstract description 36
- 239000002904 solvent Substances 0.000 title claims abstract description 24
- -1 alkyl cyanoacrylate Chemical compound 0.000 title claims abstract description 15
- 229920001651 Cyanoacrylate Polymers 0.000 title claims abstract description 12
- 229920000058 polyacrylate Polymers 0.000 title claims abstract description 10
- 230000000269 nucleophilic effect Effects 0.000 title claims abstract description 7
- 229920006243 acrylic copolymer Polymers 0.000 title claims abstract description 4
- 125000000217 alkyl group Chemical group 0.000 title abstract description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims abstract description 20
- 238000006116 polymerization reaction Methods 0.000 claims description 17
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 16
- 229920001577 copolymer Polymers 0.000 claims description 11
- FGBJXOREULPLGL-UHFFFAOYSA-N ethyl cyanoacrylate Chemical group CCOC(=O)C(=C)C#N FGBJXOREULPLGL-UHFFFAOYSA-N 0.000 claims description 11
- 229940053009 ethyl cyanoacrylate Drugs 0.000 claims description 11
- 239000003381 stabilizer Substances 0.000 claims description 9
- 229920002678 cellulose Polymers 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 229920005989 resin Polymers 0.000 claims description 6
- 239000011347 resin Substances 0.000 claims description 6
- 239000001913 cellulose Substances 0.000 claims description 5
- 150000002576 ketones Chemical class 0.000 claims description 4
- 150000003983 crown ethers Chemical class 0.000 claims description 3
- 150000001242 acetic acid derivatives Chemical class 0.000 claims description 2
- 238000010791 quenching Methods 0.000 claims description 2
- 230000000171 quenching effect Effects 0.000 claims description 2
- 210000000282 nail Anatomy 0.000 description 59
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 239000010410 layer Substances 0.000 description 12
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 8
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 8
- 239000003292 glue Substances 0.000 description 7
- 239000004926 polymethyl methacrylate Substances 0.000 description 6
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 5
- 229920000193 polymethacrylate Polymers 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- 239000013543 active substance Substances 0.000 description 4
- CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 description 4
- YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- 239000012790 adhesive layer Substances 0.000 description 3
- 150000001412 amines Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 description 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 2
- 239000004255 Butylated hydroxyanisole Substances 0.000 description 2
- 102000011782 Keratins Human genes 0.000 description 2
- 108010076876 Keratins Proteins 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 235000019282 butylated hydroxyanisole Nutrition 0.000 description 2
- 229940043253 butylated hydroxyanisole Drugs 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 210000004905 finger nail Anatomy 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- MLFHJEHSLIIPHL-UHFFFAOYSA-N isoamyl acetate Chemical compound CC(C)CCOC(C)=O MLFHJEHSLIIPHL-UHFFFAOYSA-N 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 2
- 229940011051 isopropyl acetate Drugs 0.000 description 2
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 229940090181 propyl acetate Drugs 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 2
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 2
- DSFHXKRFDFROER-UHFFFAOYSA-N 2,5,8,11,14,17-hexaoxabicyclo[16.4.0]docosa-1(22),18,20-triene Chemical compound O1CCOCCOCCOCCOCCOC2=CC=CC=C21 DSFHXKRFDFROER-UHFFFAOYSA-N 0.000 description 1
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 1
- CCTFMNIEFHGTDU-UHFFFAOYSA-N 3-methoxypropyl acetate Chemical compound COCCCOC(C)=O CCTFMNIEFHGTDU-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 239000004322 Butylated hydroxytoluene Substances 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- 229940123457 Free radical scavenger Drugs 0.000 description 1
- MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 150000001253 acrylic acids Chemical class 0.000 description 1
- 229920006397 acrylic thermoplastic Polymers 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 229940043232 butyl acetate Drugs 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 229940106189 ceramide Drugs 0.000 description 1
- 150000001783 ceramides Chemical class 0.000 description 1
- 239000013626 chemical specie Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229940093499 ethyl acetate Drugs 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 229960004337 hydroquinone Drugs 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229960003505 mequinol Drugs 0.000 description 1
- 229940016409 methylsulfonylmethane Drugs 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- HKJNHYJTVPWVGV-UHFFFAOYSA-N n,n-diethyl-4-methylaniline Chemical compound CCN(CC)C1=CC=C(C)C=C1 HKJNHYJTVPWVGV-UHFFFAOYSA-N 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 239000012038 nucleophile Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- HHVIBTZHLRERCL-UHFFFAOYSA-N sulfonyldimethane Chemical compound CS(C)(=O)=O HHVIBTZHLRERCL-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- WMOVHXAZOJBABW-UHFFFAOYSA-N tert-butyl acetate Chemical compound CC(=O)OC(C)(C)C WMOVHXAZOJBABW-UHFFFAOYSA-N 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 150000003513 tertiary aromatic amines Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/731—Cellulose; Quaternized cellulose derivatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8164—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers, e.g. poly (methyl vinyl ether-co-maleic anhydride)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q3/00—Manicure or pedicure preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
- A61K2800/95—Involves in-situ formation or cross-linking of polymers
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
Abstract
Description
KIT À BASE DE COLLE CYANOACRYLATE POUR LE MAQUILLAGE DES ONGLES La présente invention concerne un kit à base de colle cyanoacrylate pour le maquillage et/ou le soin des ongles, ainsi que son utilisation pour le maquillage et/ou le soin des ongles. Les articles de maquillage des ongles tels que les faux-ongles sont couramment utilisés par les consommateurs pour des raisons esthétiques. La pose des faux-ongles sur io les ongles nécessite alors d'utiliser des colles spécifiques afin d'obtenir une tenue satisfaisante du faux-ongle sur l'ongle. Actuellement, les colles que l'on trouve sur le marché pour coller des faux-ongles sur les ongles sont traditionnellement à base d'éthylcyanoacrylate (ou cyanoacrylate d'éthyle). Classiquement, l'éthylcyanoacrylate est utilisé en association avec un polymère 15 tel que le polyméthacrylate de méthyle, conduisant à la formation d'un système polymérisé très solide, comme décrit dans US 5,658,415. Néanmoins, ce type de colle présente l'inconvénient d'avoir une adhésion élevée, permettant certes une très bonne tenue des faux-ongles sur les ongles, mais les rendant en contrepartie difficiles à retirer lorsque le consommateur le souhaite. De plus, l'éthylcyanoacrylate présente 20 l'inconvénient d'être relativement instable et donc difficile à véhiculer. Il existe ainsi un besoin de disposer d'une colle notamment à base de cyanoacrylate d'alkyle, en particulier de cyanoacrylate d'éthyle, pour le maquillage et/ou le soin des ongles permettant de coller des faux-ongles sur les ongles de façon efficace et dont les propriétés physico-chimiques permettent un retrait facilité. 25 La présente invention a pour but de fournir un kit pour le maquillage et/ou le soin des ongles permettant de coller des articles de maquillage des ongles sur les ongles et de les retirer simplement une fois que le consommateur le souhaite. La présente invention vise également à fournir un kit comprenant du cyanoacrylate d'alkyle permettant de disposer d'une colle pour faux-ongles facile à démaquiller. 30 Ainsi, la présente invention concerne un kit pour le maquillage et/ou le soin des ongles comprenant deux compositions A et B séparées, dans lequel : la composition A comprend un cyanoacrylate d'alkyle en C1-C10 et au moins un polymère P choisi dans le groupe constitué des polymères (ALK)acryliques, des copolymères (ALK)acryliques, de leurs dérivés et de leurs mélanges, et la composition B comprend au moins un polymère P' comprenant des fonctions nucléophiles, notamment hydroxyles ou amines, et au moins un solvant volatil. Dans le cadre de la présente description, on entend par « compositions séparées » des compositions distinctes, par exemple placées dans des compartiments différents. Ainsi, les compositions A et B sont disposées dans un même kit, mais ne peuvent pas entrer en contact dans le kit. Les compositions A et B sont donc des entités distinctes. io Composition A Selon l'invention, le kit comprend une composition A comprenant un cyanoacrylate d'alkyle en Ci-Cc, avantageusement en Cl-08, de préférence en 02-08, plus préférentiellement un cyanoacrylate d'éthyle, et au moins un polymère P choisi dans le groupe constitué des polymères (ALK)acryliques, des copolymères (ALK)acryliques, de 15 leurs dérivés et de leurs mélanges. Dans le cadre de la présente description, on entend désigner par le terme « cyanoacrylate d'alkyle » un composé de formule suivante : 0 où R est un groupe alkyle. 20 Selon l'invention, R est un groupe alkyle, linéaire ou ramifié, comprenant de 1 à 10, avantageusement de 1 à 8, et de préférence de 2 à 6, atomes de carbone. Plus particulièrement, R est un groupe éthyle. Ainsi, selon un mode de réalisation avantageux, la composition A comprend du cyanoacrylate d'éthyle. 25 Avantageusement, la teneur en cyanoacrylate d'alkyle, en particulier en cyanoacrylate d'éthyle, dans la composition A est de 10% à 90%, de préférence de 50% à 90%, en poids par rapport au poids total de ladite composition. Au sens de la présente invention, le préfixe « ALK » désigne une chaîne alkyle en Cl-08. Avantageusement, il désigne une chaîne alkyle en Cl-02, de préférence un groupe 30 méthyle. Par ailleurs, on entend désigner par le terme « dérivé » (des polymères ou copolymères (ALK)acryliques) un de leurs sels, de leurs (thio)esters ou de leurs (thio)am ides.The present invention relates to a kit based on cyanoacrylate glue for the makeup and / or care of nails, as well as its use for makeup and / or care of nails. BACKGROUND OF THE INVENTION Nail makeup items such as false nails are commonly used by consumers for aesthetic reasons. The installation of false nails on the nails then requires the use of specific glues in order to obtain satisfactory holding of the false nail on the nail. Currently, glues that are found on the market for gluing nail fingernails are traditionally based on ethylcyanoacrylate (or ethyl cyanoacrylate). Typically, ethylcyanoacrylate is used in combination with a polymer such as polymethyl methacrylate, resulting in the formation of a very solid polymerized system as described in US 5,658,415. However, this type of glue has the disadvantage of having a high adhesion, allowing certainly a very good resistance to false nails on the nails, but making them in return difficult to remove when the consumer wants. In addition, the ethylcyanoacrylate has the drawback of being relatively unstable and therefore difficult to convey. There is thus a need for a glue, especially based on alkyl cyanoacrylate, in particular ethyl cyanoacrylate, for the make-up and / or care of the nails making it possible to glue false nails on the nails in such a way that effective and whose physicochemical properties allow easy removal. It is an object of the present invention to provide a makeup and / or nail care kit for adhering nails makeup articles to the nails and simply removing them after the consumer wishes. The present invention also aims to provide a kit comprising alkyl cyanoacrylate for having a false nail adhesive easy to remove. Thus, the present invention relates to a kit for makeup and / or nail care comprising two separate compositions A and B, wherein: composition A comprises a C 1 -C 10 alkyl cyanoacrylate and at least one selected P polymer in the group consisting of acrylic (ALK) polymers, acrylic (ALK) copolymers, their derivatives and their mixtures, and composition B comprises at least one polymer P 'comprising nucleophilic functions, in particular hydroxyl or amine functions, and at least a volatile solvent. In the context of the present description, the term "separate compositions" means distinct compositions, for example placed in different compartments. Thus, the compositions A and B are arranged in the same kit, but can not come into contact in the kit. Compositions A and B are therefore distinct entities. Composition A According to the invention, the kit comprises a composition A comprising a C 1 -C 8 alkyl, preferably C 1 -C 8, preferably C 2 -C 8 alkyl cyanoacrylate, more preferably an ethyl cyanoacrylate, and at least one Polymer P selected from the group consisting of acrylic (ALK) polymers, acrylic (ALK) copolymers, their derivatives and mixtures thereof. In the context of the present description, the term "alkyl cyanoacrylate" is intended to denote a compound of the following formula: ## STR2 ## where R is an alkyl group. According to the invention, R is an alkyl group, linear or branched, comprising from 1 to 10, advantageously from 1 to 8, and preferably from 2 to 6, carbon atoms. More particularly, R is an ethyl group. Thus, according to an advantageous embodiment, composition A comprises ethyl cyanoacrylate. Advantageously, the content of alkyl cyanoacrylate, in particular of ethyl cyanoacrylate, in composition A is from 10% to 90%, preferably from 50% to 90%, by weight relative to the total weight of said composition. . For the purpose of the present invention, the prefix "ALK" denotes a C1-C8 alkyl chain. Advantageously, it denotes a C1-C20 alkyl chain, preferably a methyl group. On the other hand, the term "derivative" (acrylic polymers or copolymers (ALK)) refers to one of their salts, their (thio) esters or their (thio) amides.
A titre de polymère (ALK)acrylique, on peut notamment citer les acides poly (ALK)acryliques, les poly(ALK)acrylamides, et les poly(ALK)acrylates. Parmi les poly(ALK)acrylates, on peut citer plus particulièrement les polyacrylates et les polyméthacrylates.As acrylic (ALK) polymer, there may be mentioned poly (ALK) acrylic acids, poly (ALK) acrylamides, and poly (ALK) acrylates. Among the poly (ALK) acrylates, there may be mentioned more particularly polyacrylates and polymethacrylates.
La composition A peut comprendre un polymère (ALK)acrylique seul, un copolymère (ALK)acrylique seul, un mélange de polymères(ALK)acryliques, un mélange de copolymères (ALK)acryliques ou encore un mélange de polymères (ALK)acryliques et de copolymères(ALK)acryliques. De préférence, le polymère P est choisi dans le groupe constitué des polymères (méth)acrylates, des copolymères (méth)acrylates et de leurs mélanges. Dans le cadre de la présente description, on entend désigner par « polymère ou copolymère (méth)acrylate » un polymère ou un copolymère obtenu par polymérisation radicalaire de monomères (méth)acrylate de formule X-0-C(=0)-C(R')=CH2 où R' est H ou 0H3, et X est un atome d'hydrogène ou une chaîne alkyle en Cl-020, de préférence en Cl-08. A titre de polymère (méth)acrylate, on peut notamment citer les poly(méth)acrylates d'alkyle, tels que le polyméthacrylate de méthyle, le polyméthacrylate d'éthyle, le polyméthacrylate de butyle, le polyacrylate de méthyle, le polyacrylate d'éthyle et le polyacrylate de butyle.Composition A may comprise an acrylic (ALK) polymer alone, an acrylic (ALK) copolymer alone, a mixture of acrylic (ALK) polymers, a mixture of acrylic (ALK) copolymers or a mixture of acrylic (ALK) polymers and copolymers (ALK) acrylics. Preferably, the polymer P is selected from the group consisting of (meth) acrylate polymers, (meth) acrylate copolymers and mixtures thereof. In the context of the present description, the term "polymer or copolymer (meth) acrylate" is intended to denote a polymer or copolymer obtained by radical polymerization of (meth) acrylate monomers of formula X-O-C (= O) -C ( R ') = CH2 where R' is H or OH, and X is a hydrogen atom or a C1-C20 alkyl chain, preferably C1-C8 alkyl. As the (meth) acrylate polymer, there may be mentioned in particular alkyl poly (meth) acrylates, such as polymethyl methacrylate, ethyl polymethacrylate, butyl polymethacrylate, methyl polyacrylate, polyacrylate and poly (meth) acrylate. ethyl and butyl polyacrylate.
A titre de copolymère (méth)acrylate, on peut notamment citer les copolymères de méthacrylate de méthyle et de polyméthacrylate d'éthyle. Le polymère P est par exemple le polyméthacrylate de méthyle (ou PMMA). Avantageusement, la teneur en polymère P dans la composition A est de 1% à 40%, de préférence de 5% à 25%, en poids par rapport au poids total de ladite composition. Dans le cadre de la présente invention, la composition A peut comprendre en outre au moins un stabilisant, de préférence choisi dans le groupe constitué de l'hydroquinone, de l'éther méthylique d'hydroquinone, du résorcinol, de l'hydroxyanisole butyle, de l'hydroxytoluène butyle et de leurs mélanges.As copolymer (meth) acrylate, there may be mentioned copolymers of methyl methacrylate and polymethyl methacrylate. The polymer P is, for example, polymethyl methacrylate (or PMMA). Advantageously, the content of polymer P in composition A is from 1% to 40%, preferably from 5% to 25%, by weight relative to the total weight of said composition. In the context of the present invention, the composition A may also comprise at least one stabilizer, preferably chosen from the group consisting of hydroquinone, hydroquinone methyl ether, resorcinol, butylated hydroxyanisole, butylated hydroxytoluene and mixtures thereof.
La présence de stabilisant est favorable à une meilleure stabilité de la composition dans le temps, c'est-à-dire pour éviter une gélification de la composition. Il peut s'agir d'un stabilisant seul ou d'un mélange de stabilisants. Le stabilisant est par exemple l'hydroxyanisole butyle. La teneur en stabilisant dans la composition A est généralement de 0,01% à 0,5%, de préférence de 0,05% à 0,2%, en poids par rapport au poids total de ladite composition.The presence of stabilizer is favorable to a better stability of the composition over time, that is to say to avoid gelation of the composition. It may be a stabilizer alone or a mixture of stabilizers. The stabilizer is, for example, butylated hydroxyanisole. The stabilizer content in the composition A is generally from 0.01% to 0.5%, preferably from 0.05% to 0.2%, by weight relative to the total weight of said composition.
Composition B Dans le cadre de la présente invention, le kit comprend une composition B comprenant au moins un polymère P' comprenant des fonctions nucléophiles, notamment hydroxyles ou amines, et au moins un solvant volatil.Composition B In the context of the present invention, the kit comprises a composition B comprising at least one polymer P 'comprising nucleophilic functions, in particular hydroxyl or amine functions, and at least one volatile solvent.
Dans le cadre de la présente description, on qualifie de « nucléophile » une espèce chimique qui possède une paire non liante d'électrons susceptible de participer à la formation d'une liaison. Ainsi, une espèce nucléophile est attirée par les espèces chargées positivement, par opposition à une espèce électrophile qui possède une vacance électronique susceptible d'accueillir des électrons pour former une liaison.In the context of the present description, the term "nucleophile" refers to a chemical species that has a non-binding pair of electrons capable of participating in the formation of a bond. Thus, a nucleophilic species is attracted to positively charged species, as opposed to an electrophilic species that has an electronic vacancy capable of accommodating electrons to form a bond.
Avantageusement, les fonctions nucléophiles portées par le polymère P' sont des fonctions hydroxyles ou amines. De préférence, la masse moléculaire en nombre du polymère P' est inférieure ou égale à 30 000 g/mol, avantageusement inférieure ou égale à 20 000 g/mol, de préférence de 400 g/mol à 5 000 g/mol.Advantageously, the nucleophilic functions carried by the polymer P 'are hydroxyl or amine functions. Preferably, the number-average molecular weight of the polymer P 'is less than or equal to 30,000 g / mol, advantageously less than or equal to 20,000 g / mol, preferably from 400 g / mol to 5,000 g / mol.
Selon une variante, le polymère P' est choisi dans le groupe constitué des dérivés de cellulose, des résines formaldéhyde et de leurs mélanges. A titre de dérivés de cellulose, on peut notamment citer la nitrocellulose et les esters de cellulose, tels que les acétates de cellulose, les propionates de cellulose, les butyrates de cellulose, les acétopropionates de cellulose et les acétobutyrates de cellulose. Selon une autre variante, le polymère P' est choisi parmi les résines cétone/formaldéhyde hydrogénées. Le polymère P' est par exemple la résine cétone/formaldéhyde hydrogénée commercialisée sous la dénomination TEGO VARIPLUS SK par la société EVONIK GOLDSCHMID. De préférence, la teneur en polymère P' dans la composition B est de 10% à 80%, de préférence de 35% à 65% en poids par rapport au poids total de ladite composition. Au sens de la présente invention, le terme « solvant volatil » désigne un solvant susceptible de s'évaporer au contact des matières kératiniques en moins d'une heure, à température ambiante et pression atmosphérique. Les solvants volatils de l'invention sont des solvants organiques volatils, liquides à température ambiante, ayant une pression de vapeur non nulle, à température ambiante et pression atmosphérique, allant en particulier de 0,13 Pa à 40 000 Pa (10-3 à 300 mmHg), en particulier allant de 1,3 Pa à 13 000 Pa (0,01 à 100 mmHg), et plus particulièrement allant de 1,3 Pa à 1300 Pa (0,01 à 10 mmHg).According to one variant, the polymer P 'is chosen from the group consisting of cellulose derivatives, formaldehyde resins and their mixtures. As cellulose derivatives, there may be mentioned nitrocellulose and cellulose esters, such as cellulose acetates, cellulose propionates, cellulose butyrates, cellulose acetopropionates and cellulose acetobutyrates. According to another variant, the polymer P 'is chosen from hydrogenated ketone / formaldehyde resins. The polymer P 'is, for example, the hydrogenated ketone / formaldehyde resin sold under the name TEGO VARIPLUS SK by the company Evonik GOLDSCHMID. Preferably, the content of polymer P 'in composition B is from 10% to 80%, preferably from 35% to 65% by weight relative to the total weight of said composition. For the purposes of the present invention, the term "volatile solvent" denotes a solvent capable of evaporating on contact with keratin materials in less than one hour, at ambient temperature and atmospheric pressure. The volatile solvents of the invention are volatile organic solvents which are liquid at ambient temperature and have a non-zero vapor pressure at ambient temperature and atmospheric pressure, in particular from 0.13 Pa to 40,000 Pa (10-3 to 300 mmHg), in particular ranging from 1.3 Pa to 13 000 Pa (0.01 to 100 mmHg), and more particularly ranging from 1.3 Pa to 1300 Pa (0.01 to 10 mmHg).
La composition B peut comprendre un solvant volatil seul ou un mélange de plusieurs solvants volatils. A titre de solvant volatil, on peut notamment citer l'acétone, la méthyléthylcétone, la méthylisobutylcétone, la diisobutylcétone, l'isophorone, la cyclohexanone et les acétates d'alkyle, tels que l'acétate de méthyle, l'acétate d'éthyle, l'acétate de propyle, l'acétate de n-propyle, l'acétate d'isopropyle, l'acétate de n-butyle, l'acétate d'isobutyle, l'acétate de tert-butyle et l'acétate d'isopentyle. Le solvant volatil est généralement choisi dans le groupe constitué de l'acétone, des acétates et de leurs mélanges.Composition B may comprise a volatile solvent alone or a mixture of several volatile solvents. Examples of volatile solvents that may be mentioned include acetone, methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone, isophorone, cyclohexanone and alkyl acetates, such as methyl acetate and ethyl acetate. propyl acetate, n-propyl acetate, isopropyl acetate, n-butyl acetate, isobutyl acetate, tert-butyl acetate, and acetate of isopentyl. The volatile solvent is generally selected from the group consisting of acetone, acetates, and mixtures thereof.
Avantageusement, il est choisi dans le groupe constitué de l'acétone, de l'acétate de méthyle, de l'acétate d'éthyle, de l'acétate de propyle, de l'acétate d'isopropyle, de l'acétate de butyle, de l'acétate d'isopentyle, de l'acétate de méthoxypropyle et de leurs mélanges. De préférence, le solvant volatil est constitué d'un mélange de deux solvants volatils. Selon un mode de réalisation, la composition B comprend, à titre de solvant volatil, un mélange d'acétate d'éthyle et d'acétate de butyle. Avantageusement, la teneur en solvant volatil dans la composition B est de 10% à 90%, de préférence de 35% à 75% en poids par rapport au poids total de ladite composition. Dans le cadre de la présente invention, la composition B peut comprendre en outre au moins un accélérateur de polymérisation. Il peut s'agir d'un accélérateur de polymérisation seul ou d'un mélange d'accélérateurs de polymérisation.Advantageously, it is chosen from the group consisting of acetone, methyl acetate, ethyl acetate, propyl acetate, isopropyl acetate and butyl acetate. , isopentyl acetate, methoxypropyl acetate and mixtures thereof. Preferably, the volatile solvent consists of a mixture of two volatile solvents. According to one embodiment, the composition B comprises, as a volatile solvent, a mixture of ethyl acetate and butyl acetate. Advantageously, the content of volatile solvent in the composition B is from 10% to 90%, preferably from 35% to 75% by weight relative to the total weight of said composition. In the context of the present invention, the composition B may further comprise at least one polymerization accelerator. It may be a polymerization accelerator alone or a mixture of polymerization accelerators.
Au sens de la présente invention, on entend désigner par « accélérateur de polymérisation » un composé qui augmente la vitesse d'une réaction de polymérisation. A titre d'accélérateur de polymérisation, on peut notamment citer le peroxyde de benzoyle et les amines aromatiques tertiaires, notamment la N,N-diéthyl-p-toluidine. Selon un mode de réalisation, au moins l'une des deux compositions A et B comprend en outre un accélérateur de polymérisation choisi parmi les éthers couronnes, notamment le benzo-18-crown-6. Il peut s'agir d'un accélérateur de polymérisation seul ou d'un mélange d'accélérateurs de polymérisation. Ainsi, selon ce mode de réalisation, soit la composition A seule comprend un accélérateur de polymérisation tel que défini ci-dessus, soit la composition B seule comprend un tel accélérateur de polymérisation, soit les deux compositions A et B comprennent chacune un tel accélérateur de polymérisation, les deux accélérateurs de polymérisation pouvant être identiques ou différents. Selon un autre mode de réalisation, aucune des deux compositions A et B ne comprend d'accélérateur de polymérisation choisi parmi les éthers couronnes.For the purposes of the present invention, the term "polymerization accelerator" is intended to mean a compound which increases the rate of a polymerization reaction. As a polymerization accelerator, there may be mentioned benzoyl peroxide and tertiary aromatic amines, especially N, N-diethyl-p-toluidine. According to one embodiment, at least one of the two compositions A and B further comprises a polymerization accelerator chosen from crown ethers, in particular benzo-18-crown-6. It may be a polymerization accelerator alone or a mixture of polymerization accelerators. Thus, according to this embodiment, either composition A alone comprises a polymerization accelerator as defined above, or composition B alone comprises such a polymerization accelerator, or both compositions A and B each comprise such a polymerization accelerator. polymerization, the two polymerization accelerators may be identical or different. According to another embodiment, neither of the two compositions A and B comprises a polymerization accelerator chosen from crown ethers.
Dans le cadre de l'invention, chacune des compositions A et B peut comprendre en outre d'autres ingrédients utilisés couramment dans les compositions cosmétiques et connus de l'homme du métier comme étant susceptibles d'être incorporés dans une composition adhésive pour article de maquillage des ongles. De tels ingrédients peuvent être choisis parmi les pigments et colorants, les io agents plastifiants, les agents de coalescence, les agents conservateurs, les huiles, les cires, les agents antiradicaux libres, les agents d'étalement, les agents mouillants, les agents dispersants, les anti-mousses, les conservateurs, les tensioactifs, les parfums, les neutralisants, les stabilisants, les antioxydants, les agents épaississants, les actifs pouvant être choisis parmi les huiles essentielles, les filtres UV/solaires, les agents 15 hydratants, les vitamines, les protéines, les céramides, les extraits végétaux, etc, et leurs mélanges. La composition selon l'invention peut comprendre en outre à titre d'actifs, des agents de soin des ongles tels que des agents durcissants pour matières kératiniques, des actifs agissant sur la croissance de l'ongle comme par exemple le méthyl sulfonyle 20 méthane et/ou des actifs pour traiter des affections diverses localisées au niveau de l'ongle, comme par exemple l'onichomycose. Bien entendu, l'homme du métier veillera à choisir ce ou ces éventuels composés complémentaires, et/ou leur quantité, de manière à ce que les propriétés avantageuses des compositions pour l'utilisation selon l'invention ne soient pas, ou substantiellement 25 pas, altérées par l'adjonction envisagée. La présente invention concerne également un procédé de maquillage et/ou de soin des ongles comprenant les étapes suivantes : a) application d'au moins une couche de l'une des deux compositions A ou B du kit tel que décrit plus haut sur la surface d'un ongle, pour obtenir un ongle 30 revêtu, b) application d'au moins une couche de l'autre des deux compositions du kit sous la surface d'un article de maquillage des ongles, pour obtenir un article de maquillage des ongles revêtu, et c) positionnement dudit article de maquillage des ongles revêtu obtenu à l'issue 35 de l'étape b) sur ledit ongle revêtu obtenu à l'issue de l'étape a) de façon à mettre en contact ladite couche de composition A et ladite couche de composition B, pour obtenir un ongle recouvert par un article de maquillage des ongles. Typiquement, l'article de maquillage des ongles est un faux-ongle. Plus précisément, le consommateur enduit par exemple la surface de ses ongles d'au moins une couche de composition A telle que décrite précédemment, et enduit des faux-ongles d'au moins une couche de composition B telle que décrite précédemment, puis applique les faux-ongles enduits de composition B sur ses ongles enduits de composition A. La mise en contact des compositions A et B conduit à la formation d'une couche adhésive entre l'ongle et le faux-ongle. Les ongles du consommateur sont ainsi io recouverts de faux-ongles dont la tenue est satisfaisante. Il lui est également possible d'enduire la surface de ses ongles d'au moins une couche de composition B et les faux-ongles d'au moins une couche de composition A. Enfin, la présente invention concerne un procédé de démaquillage d'un ongle recouvert par un article de maquillage des ongles susceptible d'être obtenu par un 15 procédé tel que décrit ci-dessus, comprenant le retrait dudit article de maquillage des ongles par trempe de l'ongle recouvert par l'article de maquillage des ongles dans un solvant approprié tel que l'acétone. Plus particulièrement, le consommateur peut retirer un faux-ongle collé sur un ongle à l'aide des deux compositions du kit de l'invention, en trempant l'ongle recouvert 20 du faux-ongle dans l'acétone. En effet, le solvant va dissoudre la couche adhésive qui s'est formée suite à la mise en contact des compositions A et B, permettant ainsi de retirer le faux-ongle aisément. Les pourcentages pondéraux donnés dans cette demande peuvent être assimilés 25 au pourcentage en poids en matière sèche des composés mis en oeuvre. Par « comprendre un » ou « comporter un » il convient d'entendre « comprendre au moins un » ou « comporter au moins un », sauf si le contraire est explicitement spécifié. 30 L'invention sera mieux comprise à la lecture qui va suivre, donnée uniquement à titre d'exemple. 35 EXEMPLES Exemple 1 : Préparation d'une composition A Une composition A a été préparée suivant le Tableau 1. Le mélange des composés a été réalisé sous inertage à l'azote. Tableau 1 Composé Type % en poids Ethylcyanoacrylate - 87,85 Polyméthylméthacrylate Polymère 12 Hydroxyanisole butyle (BHA) Stabilisant 0,15 Exemple 2: Préparation d'une composition B Une composition B a été préparée suivant le Tableau 2. Le mélange des composés a été réalisé sous inertage à l'azote. Tableau 2 Composé Type % en poids Résine cétone/formaldéhyde hydrogénée Polymère 87,85 (TEGO VARIPLUS SK - EVONIK GOLDSCHMID) Acétate d'éthyle Solvant 12 Acétate de butyle Solvant 0,15 Exemple 3 : Utilisation d'un kit selon l'invention Un kit selon l'invention comprenant la composition A de l'Exemple 1 et la composition B de l'Exemple 2 a été préparé puis utilisé.In the context of the invention, each of compositions A and B may further comprise other ingredients commonly used in cosmetic compositions and known to those skilled in the art as being capable of being incorporated into an adhesive composition for article of manufacture. nail makeup. Such ingredients may be selected from pigments and dyes, plasticizers, coalescers, preservatives, oils, waxes, free radical scavengers, spreading agents, wetting agents, dispersing agents, and the like. , anti-foams, preservatives, surfactants, perfumes, neutralizers, stabilizers, antioxidants, thickening agents, the active agents that may be chosen from essential oils, UV / solar filters, moisturizing agents, vitamins, proteins, ceramides, plant extracts, etc., and mixtures thereof. The composition according to the invention may furthermore comprise, as active agents, nail care agents such as hardeners for keratin materials, active agents acting on the growth of the nail, for example methylsulfonyl methane and / or active agents for treating various conditions located at the level of the nail, such as onichomycosis. Of course, those skilled in the art will take care to choose this or these optional additional compounds, and / or their quantity, so that the advantageous properties of the compositions for use according to the invention are not, or substantially not , altered by the addition envisaged. The present invention also relates to a nail makeup and / or care method comprising the following steps: a) application of at least one layer of one of the two compositions A or B of the kit as described above on the surface one nail, to obtain a coated nail, b) applying at least one layer of the other of the two compositions of the kit under the surface of a nail makeup article, to obtain a nail makeup article. coated, and c) positioning said coated nail-makeup article obtained at the end of step b) on said coated nail obtained at the end of step a) so as to contact said layer of composition A and said composition layer B, to obtain a nail covered by a nail makeup article. Typically, the article of nail makeup is a false nail. More specifically, the consumer coating, for example, the surface of his or her nails with at least one layer of composition A as described above, and coating the false nails with at least one layer of composition B as described above, then applying the False nails coated with composition B on its nails coated with composition A. The contacting of compositions A and B leads to the formation of an adhesive layer between the nail and the false nail. The consumer's nails are thus covered with false nails whose hold is satisfactory. It is also possible for it to coat the surface of its nails with at least one layer of composition B and the false nails with at least one layer of composition A. Finally, the present invention relates to a method of removing make-up from a nail covered by a nail makeup article obtainable by a method as described above, comprising removing said nail makeup article by quenching the nail covered by the nail makeup article in a suitable solvent such as acetone. More particularly, the consumer can remove a nail-sticked false nail using the two compositions of the kit of the invention, by dipping the nail covered with the false nail in acetone. Indeed, the solvent will dissolve the adhesive layer that has formed following the contacting of the compositions A and B, thereby removing the false nail easily. The weight percentages given in this application can be likened to the percentage by weight of dry matter of the compounds used. By "understand one" or "include one" it is appropriate to understand "to understand at least one" or "to include at least one", unless the contrary is explicitly specified. The invention will be better understood on reading which will be given solely by way of example. EXAMPLES Example 1: Preparation of Composition A Composition A was prepared according to Table 1. The mixture of compounds was made under nitrogen inerting. Table 1 Compound Type% by Weight Ethylcyanoacrylate - 87.85 Polymethylmethacrylate Polymer 12 Butyl Hydroxyanisole (BHA) Stabilizer 0.15 Example 2: Preparation of Composition B Composition B was prepared according to Table 2. The mixture of the compounds was carried out under nitrogen inerting. Table 2 Compound Type% by weight Resin ketone / hydrogenated formaldehyde Polymer 87.85 (TEGO VARIPLUS SK - EVONIK GOLDSCHMID) Ethyl acetate Solvent 12 Butyl acetate Solvent 0.15 Example 3: Use of a kit according to the invention A kit according to the invention comprising composition A of Example 1 and composition B of Example 2 was prepared and used.
Une couche de la composition de l'Exemple 1 a été enduite sur la surface d'un ongle et une couche de la composition de l'Exemple 2 a été enduite sous la surface d'un faux-ongle portant la référence « EDGE FASHION NAILS » de la marque FING'RSO. Le faux-ongle enduit de composition B a ensuite été appliqué sur l'ongle enduit de composition A de manière à mettre en contact la couche de la composition A avec la couche de la composition B. Les deux compositions A et B ont ainsi réagi au contact l'une de l'autre, formant une couche adhésive permettant une bonne tenue du faux-ongle. L'ongle revêtu du faux-ongle a ensuite pu être démaquillé en trempant le doigt dans de l'acétone.A layer of the composition of Example 1 was coated on the surface of a fingernail and a layer of the composition of Example 2 was coated under the surface of a false nail with the reference "EDGE FASHION NAILS From the brand FING'RSO. The counter nail with composition B was then applied to the coated nail of composition A so as to bring the layer of composition A into contact with the layer of composition B. The two compositions A and B thus reacted with contact one of the other, forming an adhesive layer for good resistance to the false nail. The nail covered with the false nail could then be cleansed by dipping the finger in acetone.
En comparaison, le même faux-ongle collé avec une composition de colle pour faux-ongles conventionnelle « Nail Glue » de la marque « France Nails® » (contenant de l'éthylcyanoacrylate, du polyméthylméthacrylate et de l'hydroquinone) n'a pas pu être décollé aussi rapidement dans les mêmes conditions.10In comparison, the same false-nail glued with a composition of glue for conventional nail-nails "Nail Glue" brand "France Nails®" (containing ethylcyanoacrylate, polymethyl methacrylate and hydroquinone) has not could be taken off as quickly under the same conditions.
Claims (17)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1261665A FR2998786B1 (en) | 2012-12-05 | 2012-12-05 | KIT BASED ON CYANOACRYLATE GLUE FOR NAIL MAKE-UP |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1261665A FR2998786B1 (en) | 2012-12-05 | 2012-12-05 | KIT BASED ON CYANOACRYLATE GLUE FOR NAIL MAKE-UP |
Publications (2)
Publication Number | Publication Date |
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FR2998786A1 true FR2998786A1 (en) | 2014-06-06 |
FR2998786B1 FR2998786B1 (en) | 2015-02-13 |
Family
ID=47628279
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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FR1261665A Expired - Fee Related FR2998786B1 (en) | 2012-12-05 | 2012-12-05 | KIT BASED ON CYANOACRYLATE GLUE FOR NAIL MAKE-UP |
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FR (1) | FR2998786B1 (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4615348A (en) * | 1981-12-11 | 1986-10-07 | Taoka Chemical Company Limited | Method for adhering artificial nail |
US5658415A (en) * | 1994-10-12 | 1997-08-19 | Montemurro; Elizabeth | Composition and process for attaching artificial nails |
US6310166B1 (en) * | 1999-08-12 | 2001-10-30 | Closure Medical Corporation | Sterilized cyanoacrylate solutions containing thickeners |
EP1900352A1 (en) * | 2006-09-13 | 2008-03-19 | L'Oréal | Nail varnish comprising a resin |
FR2940049A1 (en) * | 2008-12-23 | 2010-06-25 | Oreal | Flexible article, useful for makeup and/or care of nail and/or false nail, comprises an adhesive layer comprising a resin or natural rubber, a plasticizer and a polysaccharide or polysaccharide derivative |
-
2012
- 2012-12-05 FR FR1261665A patent/FR2998786B1/en not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4615348A (en) * | 1981-12-11 | 1986-10-07 | Taoka Chemical Company Limited | Method for adhering artificial nail |
US5658415A (en) * | 1994-10-12 | 1997-08-19 | Montemurro; Elizabeth | Composition and process for attaching artificial nails |
US6310166B1 (en) * | 1999-08-12 | 2001-10-30 | Closure Medical Corporation | Sterilized cyanoacrylate solutions containing thickeners |
EP1900352A1 (en) * | 2006-09-13 | 2008-03-19 | L'Oréal | Nail varnish comprising a resin |
FR2940049A1 (en) * | 2008-12-23 | 2010-06-25 | Oreal | Flexible article, useful for makeup and/or care of nail and/or false nail, comprises an adhesive layer comprising a resin or natural rubber, a plasticizer and a polysaccharide or polysaccharide derivative |
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FR2998786B1 (en) | 2015-02-13 |
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