WO1993018734A1 - Nail polish remover composition - Google Patents
Nail polish remover composition Download PDFInfo
- Publication number
- WO1993018734A1 WO1993018734A1 PCT/US1993/002204 US9302204W WO9318734A1 WO 1993018734 A1 WO1993018734 A1 WO 1993018734A1 US 9302204 W US9302204 W US 9302204W WO 9318734 A1 WO9318734 A1 WO 9318734A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- composition
- weight
- limonene
- cetyl acetate
- methyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 69
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 claims abstract description 87
- LSTDYDRCKUBPDI-UHFFFAOYSA-N palmityl acetate Chemical compound CCCCCCCCCCCCCCCCOC(C)=O LSTDYDRCKUBPDI-UHFFFAOYSA-N 0.000 claims abstract description 72
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims abstract description 49
- QYMFNZIUDRQRSA-UHFFFAOYSA-N dimethyl butanedioate;dimethyl hexanedioate;dimethyl pentanedioate Chemical compound COC(=O)CCC(=O)OC.COC(=O)CCCC(=O)OC.COC(=O)CCCCC(=O)OC QYMFNZIUDRQRSA-UHFFFAOYSA-N 0.000 claims abstract description 39
- 229940049297 cetyl acetate Drugs 0.000 claims abstract description 36
- 210000004905 finger nail Anatomy 0.000 claims abstract description 18
- 239000007788 liquid Substances 0.000 claims abstract description 15
- 239000004615 ingredient Substances 0.000 claims description 32
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 claims description 30
- 210000000282 nail Anatomy 0.000 claims description 23
- 229940116333 ethyl lactate Drugs 0.000 claims description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 13
- 238000004140 cleaning Methods 0.000 claims description 13
- 238000000576 coating method Methods 0.000 claims description 10
- LPEKGGXMPWTOCB-UHFFFAOYSA-N 8beta-(2,3-epoxy-2-methylbutyryloxy)-14-acetoxytithifolin Natural products COC(=O)C(C)O LPEKGGXMPWTOCB-UHFFFAOYSA-N 0.000 claims description 9
- ODQWQRRAPPTVAG-GZTJUZNOSA-N doxepin Chemical compound C1OC2=CC=CC=C2C(=C/CCN(C)C)/C2=CC=CC=C21 ODQWQRRAPPTVAG-GZTJUZNOSA-N 0.000 claims description 9
- 229940057867 methyl lactate Drugs 0.000 claims description 9
- 239000004166 Lanolin Substances 0.000 claims description 8
- 239000011248 coating agent Substances 0.000 claims description 8
- 229940039717 lanolin Drugs 0.000 claims description 8
- 235000019388 lanolin Nutrition 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 15
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
- 150000002148 esters Chemical class 0.000 description 9
- 235000019441 ethanol Nutrition 0.000 description 7
- 239000002904 solvent Substances 0.000 description 5
- XTDYIOOONNVFMA-UHFFFAOYSA-N dimethyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC XTDYIOOONNVFMA-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 4
- 231100000252 nontoxic Toxicity 0.000 description 4
- 230000003000 nontoxic effect Effects 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- -1 aliphatic dicarboxylic acids Chemical class 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 230000001532 anti-fungicidal effect Effects 0.000 description 2
- OCBHHZMJRVXXQK-UHFFFAOYSA-M benzyl-dimethyl-tetradecylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 OCBHHZMJRVXXQK-UHFFFAOYSA-M 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 235000001510 limonene Nutrition 0.000 description 2
- 229940087305 limonene Drugs 0.000 description 2
- 229940094510 myristalkonium chloride Drugs 0.000 description 2
- 231100000344 non-irritating Toxicity 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- YULGMMCZPHOUJJ-UHFFFAOYSA-N C(CCCCC(=O)OOCC)(=O)OOCC Chemical compound C(CCCCC(=O)OOCC)(=O)OOCC YULGMMCZPHOUJJ-UHFFFAOYSA-N 0.000 description 1
- CHTMQJCAYOLUKF-UHFFFAOYSA-N C(CCCCC(=O)OOCCC)(=O)OOCCC Chemical compound C(CCCCC(=O)OOCCC)(=O)OOCCC CHTMQJCAYOLUKF-UHFFFAOYSA-N 0.000 description 1
- RVXVSQKSNAOTLU-UHFFFAOYSA-N C(CCCCC(=O)OOCCCC)(=O)OOCCCC Chemical compound C(CCCCC(=O)OOCCCC)(=O)OOCCCC RVXVSQKSNAOTLU-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229940090898 Desensitizer Drugs 0.000 description 1
- UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical compound COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 150000001536 azelaic acids Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 125000001891 dimethoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/50—Solvents
- C11D7/5004—Organic solvents
- C11D7/5013—Organic solvents 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/31—Hydrocarbons
-
- 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
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4913—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q3/00—Manicure or pedicure preparations
- A61Q3/04—Nail coating removers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D9/00—Chemical paint or ink removers
- C09D9/005—Chemical paint or ink removers containing organic solvents
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/24—Hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/261—Alcohols; Phenols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/264—Aldehydes; Ketones; Acetals or ketals
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/266—Esters or carbonates
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/32—Organic compounds containing nitrogen
- C11D7/3281—Heterocyclic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/263—Ethers
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/32—Organic compounds containing nitrogen
Definitions
- the present invention relates to a coating removal and all-purpose cleaning composition and, more particularly, to a fingernail polish remover and artificial fingernail tip remover composition.
- Conventional nail polish remover compositions generally include acetone, ethyl acetate and alcohol.
- acetone, ethyl acetate and alcohol is disadvantageous in that it gives off a disagreeable odor, is irritating to the eyes and skin, and is drying to the nails and cuticles.
- Acetone, ethyl acetate and alcohol are flammable and combustible and can be harmful to the user.
- nail polish remover comprising d-limonene, N-methyl-2 pyrrolidone and cetyl acetate, and dibasic esters such as dimethyl adipate and products sold by duPont including
- dibasic ester DBE dibasic ester DBE2 or dibasic ester DBE5.
- Still another object of the present invention to provide a non-aqueous liquid cleaning composition
- composition comprising the following ingredients in
- the present invention also provides an effective, non-toxic, non-aqueous liquid finger nail cleaner composition
- an effective, non-toxic, non-aqueous liquid finger nail cleaner composition comprising the following ingredients in the general and preferred ranges set forth in approximate percent by weight: Ingredients % by weight General Preferred
- the present invention also provides a non-aqueous composition comprising the following ingredients:
- dibasic ester DEB (including dialkyl esters of dicarboxylic aliphatic acids having 4 to 12 carbon a" 3ms such as dibasic ester DBE2, dibasic ester DBE5) .
- the present invention also provides an effective, non-toxic, non-aqueous liquid finger nail cleaner, spray gun cleaner, hard surface cleaner, nail brush cleaner,
- composition comprising the following ingredients in
- compositions of the present invention while preferably used as a nail polish remover, can be used for an artificial nail tip remover, on silk line, and
- compositions are useful as all-
- the easy to use, easy to make cleaning composition is made by mixing the three liquid ingredients (d-limonene, N-methyl pyrrolidone and cetyl acetate) to form a
- the d-limonene component is a solvent or diluent that
- cleaning composition is made by mixing the four liquid
- dibasic ester DBE or dibasic ester DBE2 or dibasic ester DBE5 it should be recognized these three components can be either
- DBE2 or dibasic ester DBE5. can be in the following ratios of d-limonene to dibasic ester: 50/50 40/60 60/40 30/70 70/30
- the d-limonene helps to loosen or dissolve grease, fat or organic materials, and is described as an
- N-methyl pyrrolidone is a solvent that is compatible with d-limonene and cetyl acetate and the ingredient, preferably N-methyl 2-pyrrolidone (NMP) , is listed as a component in compositions in U.S. Patent Nos. 4,120,810 and 4,732,695.
- NMP N-methyl 2-pyrrolidone
- U.S. Patent No. 4,605,670 discloses a percutaneous (drug) absorption composition including NMP and other ingredients such as alcohols or esters including cetyl acetate.
- U.S. Patent No. 5,011,621 is a solvent that is compatible with d-limonene and cetyl acetate and the ingredient, preferably N-methyl 2-pyrrolidone (NMP)
- the cetyl acetate is a desensitizer that enhances the
- liquid non-aqueous d-limonene/NMP combination the liquid non-aqueous d-limonene/NMP combination.
- AcetulanTM a mixture of cetyl acetate and acetylated lanolin oil can be used as a substitute in whole or part for cetyl acetate. As indicated, cetyl acetate should be
- composition at least about 1/2 percent by weight of the composition with the best results being obtained with about 4 to 6 percent by weight.
- a small amount of the cetyl acetate say about 1/2 to 30 weight percent and preferably about 5 to 10% can be replaced by acetylated lanolin alcohol.
- Ethyl lactate is a solvent that
- Ethyl lactate enhances the compatibility, efficiency, miscibility, and the stability of the liquid, non-aqueous d'limonene/NMP combination and enhances the
- composition is preferably at least 45 percent by weight and more preferably at least about 50 or 55 percent by weight.
- methyl lactate can be used with
- the ethyl lactate the methyl lactate being generally
- the cleaner composition has an outstanding balance of properties including easy removal of coatings (finger nail
- polish on hard surfaces, being non-irritating, having a pleasant order, being quick drying, having miscible
- the dibasic ester is a dialkyl ester of an aliphatic dicarboxylic acid, the alkyl group having 1 to 5 carbon atoms and the aliphatic portion of the acid having
- Suitable dibasic esters are dimethoxy
- adipate dipropoxy adipate, diethoxy adipate, dibutoxy adipate as well as corresponding dialkyl esters of succinic acid and glutaric acid.
- Other suitable dialkyl esters have the acid portion derived from oxalic, malonic, pri alic and azelaic acids.
- the dibasic esters are described in duPont U.S. Patent Nos. 4,467,800, 5,096,501 and 5,002,078, incorporated herein by reference.
- dibasic ester can be used as well as small amounts, about 10 to 30% by weight, of an anti-fungicidal
- Dibasic ester DBE a preferred solvent, is a solvent that is compatible with d-limonene,
- Dibasic ester DBE or ethyl lactate enhances the compatibility, efficiency, miscibility, and the stability of the liquid, non-aqueous d'limonene/NMP combination and enhances the removal time for the more difficult hard nail polish surfaces. Best results are obtained with about 20% to 30%
- the total amount of d-limonene in the composition is
- methyl lactate can be used with the ethyl lactate, the methyl lactate being generally about 3 to 5 weight percent up to 50 to 55 weight percent of the combination of ethyl lactate and methyl lactate.
- the cleaner composition has an outstanding balance of
- polish on hard surfaces, being non-irritating, having a
- the composition can be used as an activator for a finger nail coating, it activating an acrylic compound by mixing with an acrylic powder.
- composition creates a round ball of material that is
- nail polish is applied over the hardened acrylic powder/composition coating.
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- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Animal Behavior & Ethology (AREA)
- Emergency Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
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Abstract
A liquid, non-aqueous cleaner composition that is well suited for removing finger nail polish, the composition comprising d-limonene, N-methyl pyrrolidone, cetyl acetate and, optionally, dibasic ester.
Description
TITLE NAIL POLISH REMOVER COMPOSITION FIELD OF THE INVENTION The present invention relates to a coating removal and all-purpose cleaning composition and, more particularly, to a fingernail polish remover and artificial fingernail tip remover composition.
BACKGROUND OF THE INVENTION
Conventional nail polish remover compositions generally include acetone, ethyl acetate and alcohol. The use of acetone, ethyl acetate and alcohol is disadvantageous in that it gives off a disagreeable odor, is irritating to the eyes and skin, and is drying to the nails and cuticles. Acetone, ethyl acetate and alcohol are flammable and combustible and can be harmful to the user.
OBJECTS OF THE INVENTION It is an object of the present invention to provide an easy-to-make, easy-to-use very efficient nail polish remover composition or an artificial nail remover composition and methods of using the compositions.
It is a further object of the present invention to- provide a very effective, non-toxic, non-methylene chloride, acetone, ethyl acetate or alcohol containing nail polish remover comprising d-limonene, N-methyl-2 pyrrolidone and cetyl acetate.
Still another object of the present invention to provide a non-aqueous liquid cleaning composition especially adapted for removing finger nail polish, the composition comprising the following ingredients in approximate percent by weight:
Ingredients % bv weight
1. d-limonene 5-75
2. N-methyl pyrrolidone 5-95
3. cetyl acetate 1-15
It is a further object of the present invention to
provide a very effective, non-toxic, non-methylene
chloride, acetone, ethyl acetate or alcohol containing
nail polish remover comprising d-limonene, N-methyl-2 pyrrolidone and cetyl acetate, and dibasic esters such as dimethyl adipate and products sold by duPont including
dibasic ester DBE, dibasic ester DBE2 or dibasic ester DBE5.
Still another object of the present invention to provide a non-aqueous liquid cleaning composition
especially adapted for removing finger nail polish, the
composition comprising the following ingredients in
approximate percent by weight:
Ingredients % by weight
1. d-limonene 5-75
2. N-methyl pyrrolidone 5-95
3. cetyl acetate 1-15
4. dibasic ester (DBE) 5-95
(dialkyl esters of aliphatic dicarboxylic acids)
These and other objects will be apparent from the
specification and claims that follow.
SUMMARY OF THE INVENTION The present invention provides a non-aqueous composition comprising the following ingredients:
1. d-limonene;
2. N-methyl-2 pyrrolidone; and
3. cetyl acetate.
The present invention also provides an effective, non-toxic, non-aqueous liquid finger nail cleaner composition comprising the following ingredients in the general and preferred ranges set forth in approximate percent by weight:
Ingredients % by weight General Preferred
1. d-limonene 5-75 40-70
2. N-methyl pyrrolidone 5-95 25-45
3. cetyl acetate 1-15 3-10
The present invention also provides a non-aqueous composition comprising the following ingredients:
1. d-limonene;
2. N-methyl-2 pyrrolidone;
3. cetyl acetate; and
4. dibasic ester DEB, (including dialkyl esters of dicarboxylic aliphatic acids having 4 to 12 carbon a" 3ms such as dibasic ester DBE2, dibasic ester DBE5) .
The present invention also provides an effective, non-toxic, non-aqueous liquid finger nail cleaner, spray gun cleaner, hard surface cleaner, nail brush cleaner,
etc. composition comprising the following ingredients in
the general and preferred ranges set forth in approximate percent by weight: Ingredients % by weight General Preferred
1. d-limonene 5-75 40-70
2. N-methyl pyrrolidone 5-95 25-45
3. cetyl acetate 1-15 3-10
4. dibasic ester 5-95 15-45
DETAILS OF THE INVENTION The compositions of the present invention, while preferably used as a nail polish remover, can be used for an artificial nail tip remover, on silk line, and
fiberglass wraps. The compositions are useful as all-
purpose cleaners and, in particular, hard surface cleaners, blanket washes for us in the printing industry, cleaners for brake linings, silk screens, copier belts, all kinds of metering devices including coin collecting
machines, and the cleaning of all types of spraying equipment when used for painting, applying glues, inks, greases, oils, etc. The easy to use, easy to make cleaning composition is made by mixing the three liquid ingredients (d-limonene, N-methyl pyrrolidone and cetyl acetate) to form a
homogenized stable cleaning mixture having enhanced detergent and stripping powers. When generally about one- half to 15% by weight and preferably 8 to 12% by weight of
the d-limonene is replaced by ethyl lactate, the speed of
the cleaning action increases. This combination is
necessary for the removal of some of the new hard finishes
of certain nail polishes, especially when the polishes are on wrapped nails.
The d-limonene component is a solvent or diluent that
assists in penetrating ana stripping or removing of the coating (such as finger nail polish) to be removed.
In another embodiment, easy to use, easy to make
cleaning composition is made by mixing the four liquid
ingredients - d-limonene, N-methyl pyrrolidone, cetyl acetate or a mixture of cetyl acetate and acetylated lanolin oil and dibasic ester - to form a homogenized stable cleaning mixture having enhanced detergent and stripping powers. To further clarify the use of dibasic ester DBE or dibasic ester DBE2 or dibasic ester DBE5, it should be recognized these three components can be either
blended together or incorporated separately with the same
weight proportions as the basic formulation. It should
also be recognized that d-limonene can be blended with
either of the three - dibasic ester DBE, dibasic ester
DBE2 or dibasic ester DBE5. They can be in the following ratios of d-limonene to dibasic ester:
50/50 40/60 60/40 30/70 70/30
80/20 20/80
When generally about one-half to 15% by weight and
preferably 8 to 12% by weight of the d-limonene is replaced by dibasic ester, the speed of the cleaning
action increases. This combination is necessary for the removal of some of the new hard finishes of certain nail polishes, especially when the polishes are on wrapped nails.
The d-limonene helps to loosen or dissolve grease, fat or organic materials, and is described as an
ingredient in a cleaner in U.S. Patent Nos. 4,790,951 and
5,031,648.
The N-methyl pyrrolidone is a solvent that is compatible with d-limonene and cetyl acetate and the ingredient, preferably N-methyl 2-pyrrolidone (NMP) , is listed as a component in compositions in U.S. Patent Nos. 4,120,810 and 4,732,695. U.S. Patent No. 4,605,670 discloses a percutaneous (drug) absorption composition
including NMP and other ingredients such as alcohols or esters including cetyl acetate. U.S. Patent No. 5,011,621
is directed to a paint stripper composition and discloses the use of NMP, an oil, and a plurality of cosolvents including terpenes.
The cetyl acetate is a desensitizer that enhances the
compatibility, efficiency, miscibility, and stability of
the liquid non-aqueous d-limonene/NMP combination.
Acetulan™, a mixture of cetyl acetate and acetylated lanolin oil can be used as a substitute in whole or part for cetyl acetate. As indicated, cetyl acetate should be
at least about 1/2 percent by weight of the composition with the best results being obtained with about 4 to 6 percent by weight. In some cases, a small amount of the cetyl acetate, say about 1/2 to 30 weight percent and preferably about 5 to 10% can be replaced by acetylated lanolin alcohol.
As indicated, small amounts of ethyl lactate can be
used as well as small amounts, about 1/2 to 10% by weight, of an anti-fungicidal agent, myristalkonium chloride and Quaterniun 14 (quaternary ammonium salt derivative) to enhance the cleaner composition and make it more
acceptable to the hands. Ethyl lactate is a solvent that
is compatible with d-limonene, cetyl acetate, and N-methyl
pyrrolidone. Ethyl lactate enhances the compatibility, efficiency, miscibility, and the stability of the liquid, non-aqueous d'limonene/NMP combination and enhances the
removal time for the more difficult hard nail polish surfaces. Best results are obtained with about 10% by weight and reducing d-limonene by 10% weight ethyl lactate. As indicated, the total amount of d-limonene in
the composition is preferably at least 45 percent by weight and more preferably at least about 50 or 55 percent by weight. In some cases, methyl lactate can be used with
the ethyl lactate, the methyl lactate being generally
about 3 to 5 weight percent up to 50 to 55 weight percent of the combination of ethyl lactate and methyl lactate.
The cleaner composition has an outstanding balance of properties including easy removal of coatings (finger nail
polish) on hard surfaces, being non-irritating, having a pleasant order, being quick drying, having miscible
ingredients, and leaving the cleaned surfaces free of surface fiber.
In the embodiment that optionally contains the DBE,
the dibasic ester is a dialkyl ester of an aliphatic dicarboxylic acid, the alkyl group having 1 to 5 carbon atoms and the aliphatic portion of the acid having
generally 3 or 4 carbon atoms up to as many as 10 or 12
carbon atoms. Suitable dibasic esters are dimethoxy
adipate, dipropoxy adipate, diethoxy adipate, dibutoxy adipate as well as corresponding dialkyl esters of succinic acid and glutaric acid. Other suitable dialkyl esters have the acid portion derived from oxalic, malonic, pri alic and azelaic acids. The dibasic esters are described in duPont U.S. Patent Nos. 4,467,800, 5,096,501 and 5,002,078, incorporated herein by reference.
"As indicated, preferably small amounts (15 to 30% by
weight) of dibasic ester can be used as well as small amounts, about 10 to 30% by weight, of an anti-fungicidal
agent, ethyl or methyl lactate, myristalkonium chloride and Quaterniun 14 (quaternary ammonium salt derivative) to enhance the cleaner composition and make it more acceptable to the hands. Dibasic ester DBE, a preferred solvent, is a solvent that is compatible with d-limonene,
cetyl acetate, and N-methyl pyrrolidone. Dibasic ester DBE or ethyl lactate enhances the compatibility,
efficiency, miscibility, and the stability of the liquid, non-aqueous d'limonene/NMP combination and enhances the removal time for the more difficult hard nail polish surfaces. Best results are obtained with about 20% to 30%
by weight of dibasic ester and/or ethyl lactate and reducing d-limonene by 20 to 30% by weight. As indicated, the total amount of d-limonene in the composition is
preferably at least 45 percent by weight and more
preferably at least about 50 or 55 percent by weight. In
some cases, when dibasic ester DBE is used, methyl lactate can be used with the ethyl lactate, the methyl lactate being generally about 3 to 5 weight percent up to 50 to 55 weight percent of the combination of ethyl lactate and methyl lactate.
The cleaner composition has an outstanding balance of
properties including easy removal of coatings (finger nail
polish) on hard surfaces, being non-irritating, having a
pleasant order, being quick drying, having miscible
ingredients, and leaving the cleaned surfaces free of surface fiber.
The composition can be used as an activator for a finger nail coating, it activating an acrylic compound by
mixing with an acrylic powder. The dry powder and liquid
composition creates a round ball of material that is
brushed on the fingernail. When hardened (by drying with
a dryer, for instance) nail polish is applied over the hardened acrylic powder/composition coating.
Claims
WHAT IS CLAIMED IS:
1. A non-aqueous, liquid composition comprising the following ingredients: a) d-limonene
b) N-methyl-2 pyrrolidone
c) cetyl acetate
2. A fingernail polish remover and a finger artificial nail tip remover non-aqueous composition comprising the following ingredients:
a) d-limonene b) N-methyl-2 pyrrolidone
c) cetyl acetate, the d-limonene being at least 50% by weight of the composition.
3. A non-aqueous cleaning composition comprising the following ingredients in approximate percent by weight: Ingredients % bv weight
1. d-limonene 5-75
2. N-methyl pyrrolidone 5-95
3. cetyl acetate 1-15
4. A composition as defined in claim 3 in which the following ingredients are present in approximate percent by weight: Ingredients % by weight
1. d-limonene 40-70
2. N-methyl pyrrolidone 25-45
3. cetyl acetate 3-10
5. A composition as defined in claim 3 in which the
following ingredients are present in approximate percent by weight:
Ingredients % bv weight ι. d-limonene 55-65
2. N-methyl pyrrolidone 30-40
3. cetyl acetate 4-6
6. A composition as defined in claim 3 containing about 60 weight percent d-limonene, 35 weight percent N- methyl pyrrolidone, and 5 weight percent cetyl acetate.
7. A composition as defined in claim 3 in which a
part of the d-limonene is substituted for by about 1/2 to
10 percent by weight of ethyl lactate.
8. A composition as defined in claim 3 that is effective as a fingernail polish remover and as artificial fingernail tip remover.
9. A composition as defined in claim 3 in which the d-limonene is the major component in the composition.
10. A composition as defined in claim 1 in which a
portion of the d-limonene is substituted for by ethyl lactate.
11. A composition as defined in claim 1 comprising about 50% by weight of d-limonene, about 25% by weight of N-methyl pyrrolidone, about 5% by weight of cetyl acetate
and acetylated lanolin, about 10% by weight of ethyl
lactate, and about 10% by weight of methyl lactate.
12. A liquid non-aqueous cleaner composition as
defined in claim 1, the composition being adapted to remove finger nail polish, nail wraps and tips, the
composition comprising d-limonene, N-methyl pyrrolidone,
cetyl acetate, acetylated lanolin alcohol, ethyl lactate and methyl lactate.
13. A method of removing a coating from a fingernail comprising:
a) applying a cleaning composition comprising d-limonene, NMP, a mixture of cetyl acetate and acetylated lanolin oil, and optionally, a dibasic ester to the coating on the nail; b) allowing the coated nail and composition to remain in contact for a time sufficient to loosen the
coating from the nail, and
c) separating the coating and the composition from the nail.
14. A composition as defined in claim 1 containing dibasic ester.
15. A non-aqueous, liquid composition comprising the following ingredients: a) d-limonene b) N-methyl-2 pyrrolidone
c) cetyl acetate
d) dibasic ester
16. A non-aqueous cleaning composition comprising the following ingredients in approximate percent by weight:
Ingredients % by weight
1. d-limonene 5-75
2. N-methyl pyrrolidone 5-95
3. cetyl acetate 1-15 4. dibasic ester 5-95
17. A composition as defined in claim 3 in which the
following ingredients are present in approximate percent by weight:
Ingredients % by weight
1. d-limonene 40-70
2. N-methyl pyrrolidone 25-45
3. cetyl acetate 3-10 4. dibasic ester 15-40
18. A composition as defined in claim 3 in which the following ingredients are present in approximate percent
by weight:
Ingredients % bv weight l. d-limonene 55-65
2. N-methyl pyrrolidone 30-40
3. cetyl acetate 4-6
4. dibasic ester 10-30
19. A composition as defined in claim 1 comprising about 50% by weight of d-limonene, about 25% by weight of
N-methyl pyrrolidone, about 5% by weight of cetyl acetate
and acetylated lanolin, and about 20% by weight of dibasic ester.
20. A liquid non-aqueous cleaner composition as defined in claim 1, the composition being adapted to remove finger nail polish, nail wraps and tips, the
composition comprising d-limonene, N-methyl pyrrolidone, cetyl acetate, acetylated lanolin alcohol, and dibasic
ester.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/851,738 | 1992-03-16 | ||
| US07/851,738 US5346652A (en) | 1992-03-16 | 1992-03-16 | Nail polish remover composition |
| US07/866,793 | 1992-04-08 | ||
| US07/866,793 US5360580A (en) | 1992-04-08 | 1992-04-08 | Cleaning composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1993018734A1 true WO1993018734A1 (en) | 1993-09-30 |
Family
ID=27127019
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US1993/002204 WO1993018734A1 (en) | 1992-03-16 | 1993-03-11 | Nail polish remover composition |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO1993018734A1 (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6689727B1 (en) | 1999-01-20 | 2004-02-10 | Bozena Olsson | Agent for removing adhesive products |
| DE19861089B4 (en) * | 1998-12-30 | 2007-12-27 | Sven Langenhan | Process for cleaning heat transfer systems |
| US20200139163A1 (en) * | 2018-11-07 | 2020-05-07 | Jake Palmer | Compositions For Removing Surface Coatings |
| WO2020166750A1 (en) * | 2019-02-15 | 2020-08-20 | 배준용 | Retouching makeup remover and method for preparing same |
| WO2024232149A1 (en) * | 2023-05-10 | 2024-11-14 | 冨士色素株式会社 | Nail polish remover |
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| US3686701A (en) * | 1969-02-04 | 1972-08-29 | Oreal | Cosmetic composition containing microencapsulated solvents for nail enamel |
| US4533487A (en) * | 1983-08-15 | 1985-08-06 | Pitre-Jones | Process for producing blended d-Limonene and uses of the blended product |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19861089B4 (en) * | 1998-12-30 | 2007-12-27 | Sven Langenhan | Process for cleaning heat transfer systems |
| US6689727B1 (en) | 1999-01-20 | 2004-02-10 | Bozena Olsson | Agent for removing adhesive products |
| US20200139163A1 (en) * | 2018-11-07 | 2020-05-07 | Jake Palmer | Compositions For Removing Surface Coatings |
| WO2020166750A1 (en) * | 2019-02-15 | 2020-08-20 | 배준용 | Retouching makeup remover and method for preparing same |
| WO2024232149A1 (en) * | 2023-05-10 | 2024-11-14 | 冨士色素株式会社 | Nail polish remover |
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