CA1067012A - Ongles artificiels a durcissement spontane - Google Patents

Ongles artificiels a durcissement spontane

Info

Publication number: CA1067012A
Authority: CA; Canada
Prior art keywords: composition; monomer; nail; curing; initiator
Prior art date: 1974-11-26
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

CA240,603A

Other languages

English (en)

Inventor

Henry L. Lee (Jr.)

Jan A. Orlowski

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Lee Pharmaceuticals Inc

Original Assignee

Lee Pharmaceuticals Inc

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1974-11-26

Filing date

1975-11-25

Publication date

1979-11-27

1975-11-25 Application filed by Lee Pharmaceuticals Inc filed Critical Lee Pharmaceuticals Inc

1979-11-27 Application granted granted Critical

1979-11-27 Publication of CA1067012A publication Critical patent/CA1067012A/fr

Status Expired legal-status Critical Current

Links

210000004905 finger nail Anatomy 0.000 title claims abstract description 15
239000000203 mixture Substances 0.000 claims abstract description 136
239000000178 monomer Substances 0.000 claims abstract description 65
239000003999 initiator Substances 0.000 claims abstract description 47
238000000034 method Methods 0.000 claims abstract description 23
238000004132 cross linking Methods 0.000 claims abstract description 15
230000000379 polymerizing effect Effects 0.000 claims abstract 2
210000000282 nail Anatomy 0.000 claims description 72
239000004615 ingredient Substances 0.000 claims description 19
-1 methacryloyl Chemical group 0.000 claims description 16
238000002156 mixing Methods 0.000 claims description 16
239000002202 Polyethylene glycol Substances 0.000 claims description 15
239000011248 coating agent Substances 0.000 claims description 15
238000000576 coating method Methods 0.000 claims description 15
239000000945 filler Substances 0.000 claims description 15
239000000463 material Substances 0.000 claims description 15
229920001223 polyethylene glycol Polymers 0.000 claims description 15
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 14
239000001301 oxygen Substances 0.000 claims description 14
229910052760 oxygen Inorganic materials 0.000 claims description 14
238000006116 polymerization reaction Methods 0.000 claims description 14
239000004342 Benzoyl peroxide Substances 0.000 claims description 12
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims description 12
235000019400 benzoyl peroxide Nutrition 0.000 claims description 12
XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 claims description 11
229920001577 copolymer Polymers 0.000 claims description 11
STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims description 11
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 10
LCXXNKZQVOXMEH-UHFFFAOYSA-N Tetrahydrofurfuryl methacrylate Chemical compound CC(=C)C(=O)OCC1CCCO1 LCXXNKZQVOXMEH-UHFFFAOYSA-N 0.000 claims description 10
238000009472 formulation Methods 0.000 claims description 9
150000003254 radicals Chemical class 0.000 claims description 8
238000011065 in-situ storage Methods 0.000 claims description 7
239000000758 substrate Substances 0.000 claims description 7
MUTNCGKQJGXKEM-UHFFFAOYSA-N tamibarotene Chemical compound C=1C=C2C(C)(C)CCC(C)(C)C2=CC=1NC(=O)C1=CC=C(C(O)=O)C=C1 MUTNCGKQJGXKEM-UHFFFAOYSA-N 0.000 claims description 7
HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical group CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 claims description 6
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 6
239000004641 Diallyl-phthalate Substances 0.000 claims description 6
125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 claims description 6
QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 claims description 6
239000003795 chemical substances by application Substances 0.000 claims description 6
FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 claims description 6
KVVZUKZKXMVBNM-UHFFFAOYSA-N 2-methyl-5-[4-[2-[4-(4-methyl-3-oxopent-4-enoxy)phenyl]propan-2-yl]phenoxy]pent-1-en-3-one Chemical compound C1=CC(OCCC(=O)C(=C)C)=CC=C1C(C)(C)C1=CC=C(OCCC(=O)C(C)=C)C=C1 KVVZUKZKXMVBNM-UHFFFAOYSA-N 0.000 claims description 5
ZPOLOEWJWXZUSP-AATRIKPKSA-N bis(prop-2-enyl) (e)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C\C(=O)OCC=C ZPOLOEWJWXZUSP-AATRIKPKSA-N 0.000 claims description 5
239000001294 propane Substances 0.000 claims description 5
JLMVPAPCBSCTAZ-UHFFFAOYSA-N 2-methyl-1-[4-[2-[4-(2-methylprop-2-enoyl)phenyl]propan-2-yl]phenyl]prop-2-en-1-one Chemical compound C1=CC(C(=O)C(=C)C)=CC=C1C(C)(C)C1=CC=C(C(=O)C(C)=C)C=C1 JLMVPAPCBSCTAZ-UHFFFAOYSA-N 0.000 claims description 4
UIPXAHZROJKXQV-UHFFFAOYSA-N 3-oxopent-4-enyl 2-methylprop-2-enoate Chemical class CC(=C)C(=O)OCCC(=O)C=C UIPXAHZROJKXQV-UHFFFAOYSA-N 0.000 claims description 4
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 4
229920006037 cross link polymer Polymers 0.000 claims description 4
150000002978 peroxides Chemical class 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 claims description 3
HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 claims description 3
150000003512 tertiary amines Chemical class 0.000 claims description 3
ZAJCJTYYSXOWAY-UHFFFAOYSA-N 5-hydroxy-6-[4-[2-[4-(2-hydroxy-5-methyl-4-oxohex-5-enoxy)phenyl]propan-2-yl]phenoxy]-2-methylhex-1-en-3-one Chemical group C1=CC(OCC(O)CC(=O)C(=C)C)=CC=C1C(C)(C)C1=CC=C(OCC(O)CC(=O)C(C)=C)C=C1 ZAJCJTYYSXOWAY-UHFFFAOYSA-N 0.000 claims 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims 3
229920006395 saturated elastomer Polymers 0.000 claims 1
239000000843 powder Substances 0.000 description 16
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 14
239000007788 liquid Substances 0.000 description 14
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical group COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 12
239000003054 catalyst Substances 0.000 description 10
FEXBEKLLSUWSIM-UHFFFAOYSA-N 2-Butyl-4-methylphenol Chemical compound CCCCC1=CC(C)=CC=C1O FEXBEKLLSUWSIM-UHFFFAOYSA-N 0.000 description 9
239000000975 dye Substances 0.000 description 8
GYVGXEWAOAAJEU-UHFFFAOYSA-N n,n,4-trimethylaniline Chemical compound CN(C)C1=CC=C(C)C=C1 GYVGXEWAOAAJEU-UHFFFAOYSA-N 0.000 description 8
239000003381 stabilizer Substances 0.000 description 8
239000004408 titanium dioxide Substances 0.000 description 7
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
239000006096 absorbing agent Substances 0.000 description 6
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
229920003229 poly(methyl methacrylate) Polymers 0.000 description 4
229920000642 polymer Polymers 0.000 description 4
239000004926 polymethyl methacrylate Substances 0.000 description 4
125000000217 alkyl group Chemical group 0.000 description 3
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 3
239000012965 benzophenone Substances 0.000 description 3
SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 3
235000012239 silicon dioxide Nutrition 0.000 description 3
AHSGHEXYEABOKT-UHFFFAOYSA-N 2-[2-(2-benzoyloxyethoxy)ethoxy]ethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCCOCCOCCOC(=O)C1=CC=CC=C1 AHSGHEXYEABOKT-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
230000001680 brushing effect Effects 0.000 description 2
239000002537 cosmetic Substances 0.000 description 2
229910002026 crystalline silica Inorganic materials 0.000 description 2
239000011953 free-radical catalyst Substances 0.000 description 2
DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
229920000058 polyacrylate Polymers 0.000 description 2
239000000126 substance Substances 0.000 description 2
229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
JUVSRZCUMWZBFK-UHFFFAOYSA-N 2-[n-(2-hydroxyethyl)-4-methylanilino]ethanol Chemical compound CC1=CC=C(N(CCO)CCO)C=C1 JUVSRZCUMWZBFK-UHFFFAOYSA-N 0.000 description 1
WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 description 1
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
SOJFOOLKALJHGL-UHFFFAOYSA-N C1(CCCC1)OC(C=1C(C(=O)O)=CC=CC1)=O Chemical compound C1(CCCC1)OC(C=1C(C(=O)O)=CC=CC1)=O SOJFOOLKALJHGL-UHFFFAOYSA-N 0.000 description 1
201000004624 Dermatitis Diseases 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
208000027418 Wounds and injury Diseases 0.000 description 1
230000005856 abnormality Effects 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
150000001448 anilines Chemical class 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000008119 colloidal silica Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000010276 construction Methods 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
WRAABIJFUKKEJQ-UHFFFAOYSA-N cyclopentyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCC1 WRAABIJFUKKEJQ-UHFFFAOYSA-N 0.000 description 1
BTQLDZMOTPTCGG-UHFFFAOYSA-N cyclopentyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCC1 BTQLDZMOTPTCGG-UHFFFAOYSA-N 0.000 description 1
230000006378 damage Effects 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
230000002526 effect on cardiovascular system Effects 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
OAPHLAAOJMTMLY-UHFFFAOYSA-N ethyl 2-methylbut-2-enoate Chemical compound CCOC(=O)C(C)=CC OAPHLAAOJMTMLY-UHFFFAOYSA-N 0.000 description 1
230000002068 genetic effect Effects 0.000 description 1
239000011521 glass Substances 0.000 description 1
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
208000014674 injury Diseases 0.000 description 1
239000011256 inorganic filler Substances 0.000 description 1
229910003475 inorganic filler Inorganic materials 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
239000008155 medical solution Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000003607 modifier Substances 0.000 description 1
PMDKYLLIOLFQPO-UHFFFAOYSA-N monocyclohexyl phthalate Chemical compound OC(=O)C1=CC=CC=C1C(=O)OC1CCCCC1 PMDKYLLIOLFQPO-UHFFFAOYSA-N 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
230000036562 nail growth Effects 0.000 description 1
150000001451 organic peroxides Chemical class 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
125000005498 phthalate group Chemical class 0.000 description 1
229920001483 poly(ethyl methacrylate) polymer Polymers 0.000 description 1
229920000120 polyethyl acrylate Polymers 0.000 description 1
239000002243 precursor Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
230000037390 scarring Effects 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
210000004906 toe nail Anatomy 0.000 description 1
150000004992 toluidines Chemical class 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- 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
- 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

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)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Adhesives Or Adhesive Processes (AREA)
Materials For Medical Uses (AREA)
Cosmetics (AREA)
Paints Or Removers (AREA)

CA240,603A 1974-11-26 1975-11-25 Ongles artificiels a durcissement spontane Expired CA1067012A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US52722174A	1974-11-26	1974-11-26

Publications (1)

Publication Number	Publication Date
CA1067012A true CA1067012A (fr)	1979-11-27

Family

ID=24100609

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA240,603A Expired CA1067012A (fr)	1974-11-26	1975-11-25	Ongles artificiels a durcissement spontane

Country Status (5)

Country	Link
JP (1)	JPS5192246A (fr)
CA (1)	CA1067012A (fr)
DE (1)	DE2553138A1 (fr)
FR (1)	FR2292463A1 (fr)
GB (1)	GB1514549A (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2718017C3 (de) *	1977-04-22	1988-10-20	Hofacker, geb. Schlüter, Frauke, Freifrau von Nostitz, 8000 München	Verwendung einer selbsthärtenden Masse zur direkten Unterfütterung von Prothesen im Mund
DE3727916A1 (de) *	1987-08-21	1989-03-02	Kulzer & Co Gmbh	Fingernagel-bestrahlungsgeraet
AT412874B (de) *	2004-04-23	2005-08-25	Invicon Chemical Solutions Gmb	Reparaturset

1975
- 1975-11-25 GB GB4831275A patent/GB1514549A/en not_active Expired
- 1975-11-25 CA CA240,603A patent/CA1067012A/fr not_active Expired
- 1975-11-26 JP JP50141794A patent/JPS5192246A/ja active Pending
- 1975-11-26 FR FR7536132A patent/FR2292463A1/fr not_active Withdrawn
- 1975-11-26 DE DE19752553138 patent/DE2553138A1/de active Pending

Also Published As

Publication number	Publication date
FR2292463A1 (fr)	1976-06-25
JPS5192246A (fr)	1976-08-12
DE2553138A1 (de)	1976-08-12
GB1514549A (en)	1978-06-14

Publication	Publication Date	Title
US4229431A (en)	1980-10-21	Method of applying self curing artificial nails
US4104333A (en)	1978-08-01	Self-curing artificial fingernails
RU2560249C2 (ru)	2015-08-20	Удаляемый цветной слой для покрытий искусственных ногтей и связанные с этим способы
US6472453B2 (en)	2002-10-29	Compositions for making an artificial prosthesis
US4863993A (en)	1989-09-05	Surface priming composition for proteinaceous substrates; method of making and using same
US9717672B2 (en)	2017-08-01	Compositions and methods for UV-curable cosmetic nail coatings
EP3029114B1 (fr)	2021-03-03	System pour recruvement de surface d'ongle
CA2021570C (fr)	2002-12-17	Composition de liant topique a base de copolymere a polysiloxane greffe, avec de nouveaux monomeres hydrophiles et methode de revetement avec celui-ci
Swift et al.	1995	Shear bond strengths of resin-modified glass-ionomer restorative materials
US4495172A (en)	1985-01-22	Nail coating
KR20010071117A (ko)	2001-07-28	인조 손톱 조성물 및 그 제조방법
US4708866A (en)	1987-11-24	Artificial nail composition
US4394494A (en)	1983-07-19	Dental filling material
EP0832638A3 (fr)	1999-03-24	Composition cosmetique aqueuse ou aqueuse-alcoolique pour les cheveux
US6455033B1 (en)	2002-09-24	Artificial nails
CA1067012A (fr)	1979-11-27	Ongles artificiels a durcissement spontane
US4913939A (en)	1990-04-03	Method of making and using surface priming composition for proteinaceous substrates
EP2218435A1 (fr)	2010-08-18	Initiateurs dans deux composants et composition polymérisable l'utilisant
US5037638A (en)	1991-08-06	Fluoride release agent copolymer prepared using morpholinoethyl methacrylate hydrofluoride comonomer
US11000469B1 (en)	2021-05-11	Nail gel builder composition
EP3596177B1 (fr)	2023-11-29	Solution inodore de monomère durcissable par uv
JPH09324019A (ja)	1997-12-16	硬化性組成物
US20170137554A1 (en)	2017-05-18	A multi-part acrylic cold-curing composition
GB2643527A (en)	2026-02-25	Liquid monomer compositions
JPH04366112A (ja)	1992-12-18	可視光重合硬化性組成物