EP0405664B1 - Produit pour le nettoyage corporel avec polymère cationique à groupe amine encombrante et odeur compatible - Google Patents
Produit pour le nettoyage corporel avec polymère cationique à groupe amine encombrante et odeur compatible Download PDFInfo
- Publication number
- EP0405664B1 EP0405664B1 EP90201638A EP90201638A EP0405664B1 EP 0405664 B1 EP0405664 B1 EP 0405664B1 EP 90201638 A EP90201638 A EP 90201638A EP 90201638 A EP90201638 A EP 90201638A EP 0405664 B1 EP0405664 B1 EP 0405664B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- alkyl
- cationic
- weight
- personal cleansing
- polymer
- Prior art date
- 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 - Lifetime
Links
- 150000001412 amines Chemical class 0.000 title claims description 29
- 229920006317 cationic polymer Polymers 0.000 title claims description 22
- 239000000203 mixture Substances 0.000 claims description 66
- 229920000642 polymer Polymers 0.000 claims description 33
- 239000000344 soap Substances 0.000 claims description 33
- -1 hydroxy ethyl group Chemical group 0.000 claims description 28
- 239000004094 surface-active agent Substances 0.000 claims description 22
- 125000002091 cationic group Chemical group 0.000 claims description 20
- 235000012149 noodles Nutrition 0.000 claims description 9
- 229910052783 alkali metal Inorganic materials 0.000 claims description 8
- 150000001340 alkali metals Chemical class 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 229920002907 Guar gum Polymers 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000000665 guar gum Substances 0.000 claims description 6
- 235000010417 guar gum Nutrition 0.000 claims description 6
- 229960002154 guar gum Drugs 0.000 claims description 6
- 238000003801 milling Methods 0.000 claims description 6
- 238000009835 boiling Methods 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- 150000001720 carbohydrates Chemical class 0.000 claims description 4
- 229920003118 cationic copolymer Polymers 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000000178 monomer Substances 0.000 claims description 3
- 229920001282 polysaccharide Polymers 0.000 claims description 3
- 239000005017 polysaccharide Substances 0.000 claims description 3
- 229920001059 synthetic polymer Polymers 0.000 claims description 3
- RMTFNDVZYPHUEF-XZBKPIIZSA-N 3-O-methyl-D-glucose Chemical class O=C[C@H](O)[C@@H](OC)[C@H](O)[C@H](O)CO RMTFNDVZYPHUEF-XZBKPIIZSA-N 0.000 claims description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- 150000003973 alkyl amines Chemical class 0.000 claims description 2
- 150000008051 alkyl sulfates Chemical class 0.000 claims description 2
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
- 229930182478 glucoside Natural products 0.000 claims description 2
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims description 2
- 229920001296 polysiloxane Polymers 0.000 claims description 2
- 102000004169 proteins and genes Human genes 0.000 claims description 2
- 108090000623 proteins and genes Proteins 0.000 claims description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 12
- 239000000194 fatty acid Substances 0.000 description 12
- 229930195729 fatty acid Natural products 0.000 description 12
- 150000004665 fatty acids Chemical class 0.000 description 12
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 12
- 239000000463 material Substances 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 210000003491 skin Anatomy 0.000 description 7
- 239000000271 synthetic detergent Substances 0.000 description 7
- 244000060011 Cocos nucifera Species 0.000 description 6
- 235000013162 Cocos nucifera Nutrition 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 230000003750 conditioning effect Effects 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
- 239000003760 tallow Substances 0.000 description 5
- 239000003240 coconut oil Substances 0.000 description 4
- 235000019864 coconut oil Nutrition 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 239000002304 perfume Substances 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 244000303965 Cyamopsis psoralioides Species 0.000 description 3
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 3
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 150000001342 alkaline earth metals Chemical class 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 235000021588 free fatty acids Nutrition 0.000 description 3
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000004166 Lanolin Substances 0.000 description 2
- 239000004909 Moisturizer Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000003242 anti bacterial agent Substances 0.000 description 2
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 2
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 2
- MSWZFWKMSRAUBD-UHFFFAOYSA-N beta-D-galactosamine Natural products NC1C(O)OC(CO)C(O)C1O MSWZFWKMSRAUBD-UHFFFAOYSA-N 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 229940039717 lanolin Drugs 0.000 description 2
- 235000019388 lanolin Nutrition 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000001333 moisturizer Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- MSWZFWKMSRAUBD-GASJEMHNSA-N 2-amino-2-deoxy-D-galactopyranose Chemical compound N[C@H]1C(O)O[C@H](CO)[C@H](O)[C@@H]1O MSWZFWKMSRAUBD-GASJEMHNSA-N 0.000 description 1
- MSWZFWKMSRAUBD-IVMDWMLBSA-N 2-amino-2-deoxy-D-glucopyranose Chemical compound N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O MSWZFWKMSRAUBD-IVMDWMLBSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical class C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- SHZGCJCMOBCMKK-UHFFFAOYSA-N D-mannomethylose Natural products CC1OC(O)C(O)C(O)C1O SHZGCJCMOBCMKK-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- PNNNRSAQSRJVSB-SLPGGIOYSA-N Fucose Natural products C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C=O PNNNRSAQSRJVSB-SLPGGIOYSA-N 0.000 description 1
- 229920000926 Galactomannan Polymers 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- SHZGCJCMOBCMKK-DHVFOXMCSA-N L-fucopyranose Chemical compound C[C@@H]1OC(O)[C@@H](O)[C@H](O)[C@@H]1O SHZGCJCMOBCMKK-DHVFOXMCSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- SVYKKECYCPFKGB-UHFFFAOYSA-N N,N-dimethylcyclohexylamine Chemical compound CN(C)C1CCCCC1 SVYKKECYCPFKGB-UHFFFAOYSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- 244000021150 Orbignya martiana Species 0.000 description 1
- 235000014643 Orbignya martiana Nutrition 0.000 description 1
- 241000282372 Panthera onca Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- IAJILQKETJEXLJ-RSJOWCBRSA-N aldehydo-D-galacturonic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-RSJOWCBRSA-N 0.000 description 1
- IAJILQKETJEXLJ-QTBDOELSSA-N aldehydo-D-glucuronic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-QTBDOELSSA-N 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
- 229920006318 anionic polymer Polymers 0.000 description 1
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 239000012972 dimethylethanolamine Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229940071106 ethylenediaminetetraacetate Drugs 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 229960002442 glucosamine Drugs 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229940097043 glucuronic acid Drugs 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- ZFSXZJXLKAJIGS-UHFFFAOYSA-N halocarban Chemical compound C1=C(Cl)C(C(F)(F)F)=CC(NC(=O)NC=2C=CC(Cl)=CC=2)=C1 ZFSXZJXLKAJIGS-UHFFFAOYSA-N 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000004029 hydroxymethyl group Chemical class [H]OC([H])([H])* 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- XGZOMURMPLSSKQ-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)N(CCO)CCO XGZOMURMPLSSKQ-UHFFFAOYSA-N 0.000 description 1
- DAZXVJBJRMWXJP-UHFFFAOYSA-N n,n-dimethylethylamine Chemical compound CCN(C)C DAZXVJBJRMWXJP-UHFFFAOYSA-N 0.000 description 1
- UQKAOOAFEFCDGT-UHFFFAOYSA-N n,n-dimethyloctan-1-amine Chemical compound CCCCCCCCN(C)C UQKAOOAFEFCDGT-UHFFFAOYSA-N 0.000 description 1
- GNVRJGIVDSQCOP-UHFFFAOYSA-N n-ethyl-n-methylethanamine Chemical compound CCN(C)CC GNVRJGIVDSQCOP-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000006174 pH buffer Substances 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 150000004671 saturated fatty acids Chemical group 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 210000000434 stratum corneum Anatomy 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000012956 testing procedure Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- KVSKGMLNBAPGKH-UHFFFAOYSA-N tribromosalicylanilide Chemical class OC1=C(Br)C=C(Br)C=C1C(=O)NC1=CC=C(Br)C=C1 KVSKGMLNBAPGKH-UHFFFAOYSA-N 0.000 description 1
- ICUTUKXCWQYESQ-UHFFFAOYSA-N triclocarban Chemical compound C1=CC(Cl)=CC=C1NC(=O)NC1=CC=C(Cl)C(Cl)=C1 ICUTUKXCWQYESQ-UHFFFAOYSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 125000005314 unsaturated fatty acid group Chemical group 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
- C11D3/3742—Nitrogen containing silicones
-
- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0047—Detergents in the form of bars or tablets
- C11D17/006—Detergents in the form of bars or tablets containing mainly surfactants, but no builders, e.g. syndet bar
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
- C11D3/227—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin with nitrogen-containing groups
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3769—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3769—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
- C11D3/3773—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines in liquid compositions
Definitions
- compositions for personal washing which compositions comprise quaternary amine polymers.
- Liquid and solid bar compositions based on soap and/or synthetic surfactants are commonly used for cleansing the human body.
- a wide variety of additives have been suggested for inclusion in said compositions. Some enhance the physical properties, e.g., bar hardness, wear rate, resistance to water. Others enhance the in-use properties such as lather characteristics and some impact on the impression the composition has on the skin both during washing (bar feel) and afterwards.
- the useful polymers should be soluble or dispersible in water to a level of at least 1% by weight, preferably at least 5% by weight at 25°C.
- Suitable polymers are high molecular weight materials (mass-average molecular weight determined, for instance, by light scattering, being generally from 20,000 to 5,000,000, preferably from 50,000 to 4,000,000, and more preferably from 500,000 to 3,000,000) and preferably have a thickening ability such that a 1% dispersion of the polymer in water at 20°C exceeds 1 Pa ⁇ S (10 poise) at a shear rate of 10 ⁇ sec-1.
- Useful polymers are the cationic, nonionic, amphoteric, and anionic polymers useful in the cosmetic field. Preferred are cationic and nonionic resins and mixtures thereof. Highly preferred are the cationic resins.
- the preferred cationic polymers include cationic guar gums such as hydroxyproxyltrimethylammonium guar gum.
- cationic guar gums such as hydroxyproxyltrimethylammonium guar gum.
- cationic trimethylamine quaternized polymers in compositions having a pH of 7.5 or above. They break down and release odoriferous labile amines.
- the present invention relates to a personal cleansing product in the form of a toilet bar made with a selected quaternized cationic polymer wherein each quaternary ammonium moiety is derived from a bulky amine.
- An object of the present invention is to provide an improved toilet soap bar comprising a cationic polymeric skin conditioning agent which does not comprise a potential odoriferous amine moiety.
- the present invention comprises basic personal cleansing compositions comprising from 0.2% to 5% by weight selected cationic polymer wherein each cationic group is derived from a "bulky” amine.
- each cationic group is derived from a "bulky” amine.
- the compositions of this invention consistently exhibit superior odor stability due to the selected "bulky amine" cationic polymers.
- basic personal cleansing compositions as used herein means that the composition has a pH of at least 8.5.
- illustrations A and B show the theoretical degradation of labile amine containing cationic polymers in a basic environment.
- R1-R3 is H or any other substituent and R4, R5 and R6 combine with N to form an amine with less odor impact than trimethylamine, at least one of R4, R5 and R6 is alkyl having a chain length of from 2 to 24 carbon atoms, or an alkoxy alkyl group containing from 2 to 12 carbon atoms or a hydroxy ethyl group.
- cationic guar gums having the following structures:
- HEC bulky amine hydroxyethyl cellulose
- the composition of this invention comprises from 0.2% to 5%, preferably from 0.5% to 2% by weight, of the cationic polymer.
- the average molecular weight of the preferred cationic guar gum is from 50,000 to 1,000,000, preferably from 100,000 to 500,000, and more preferably from 250,000 to 400,000 and the degree of substitution is from 0.5 to 4, preferably from 1 to 2.5.
- Some preferred cationic guars (galactomannans) are disclosed in US-A-4,758,282, Stober et al., issued July 19, 1988.
- bulky amine cationic polymeric skin conditioning agents useful in the present invention have molecular weights of from 1,000 to 3,000,000.
- Useful polymers are selected from the group consisting of:
- members of the bulky amine cationic polysaccharide class include the cationic hydroxyethyl cellulose, e.g., LM-200 (RTM) made by Union Carbide Corporation.
- the cationic copolymers of saccharides and synthetic cationic monomers useful in the present invention encompass those containing the following saccharides: glucose, galactose, mannose, arabinose, xylose, fucose, fructose, glucosamine, galactosamine, glucuronic acid, galacturonic acid, and 5 or 6 membered ring polyalcohols. Also included are hydroxymethyl, hydroxyethyl and hydroxypropyl derivatives of the above sugars.
- volatility decreases with increasing molecular weight. Volatility is dependent, among other things on the boiling point of the neat component. Odor impact also has a strong dependence on the amount of volatilized material that reaches the nose. Table 1 demonstrates the significant effect which adding "bulky” groups has on volatility and, hence, odor impact of amines. For pure hydrocarbon substitution, the larger the alkyl chains (or the larger the degree of long chain substitution) the lower the odor impact.
- the quaternised cationic polymers used in the present invention have an ammonium moiety derived from bulky amines having boiling points of greater than 80°C.
- the surfactant component of the present compositions comprises alkali metal soap or mixtures of alkali metal soap and synthetic surfactant.
- Alkali metal soaps can be made by direct saponification of the fats and oils or by the neutralization of the free fatty acids which are prepared in a separate manufacturing process. Particularly useful are the sodium and potassium salts of the mixtures of fatty acids derived from coconut oil and tallow, i.e., sodium and potassium tallow and coconut soaps.
- tallow is used herein in connection with fatty acid mixtures which typically have an approximate carbon chain length distribution of 2.5% C14, 29% C16, 23% C18, 2% palmitoleic, 41.5% oleic and 3% linoleic. (The first three fatty acids listed are saturated.) Other mixtures with similar distribution, such as the fatty acids derived from various animal tallows. The tallow can also be hardened (i.e., hydrogenated) to convert part or all of the unsaturated fatty acid moieties to saturated fatty acid moieties.
- coconut oil and “coconut fatty acid” (CNFA) are used herein, they refer to fatty acid mixtures which typically have an approximate carbon chain length distribution of about 8% C7, 7% C10, 48% C12, 17% C14, 9% C16, 2% C18, 7% oleic, and 2% linoleic. (The first six fatty acids listed are saturated.) Other sources having similar carbon chain length distribution such as palm kernel oil and babassu kernel oil are included with the terms coconut oil and coconut fatty acid.
- a preferred soap bar of this invention comprises soap as its primary or sole surfactant. It also contains as an essential ingredient a skin conditioning amount of a hydrated, cationic guar gum provided by a cationic guar gum polymer. This polymer is uniformly distributed in the soap bar matrix without affecting the smooth feel of the dry or wet bar.
- Another preferred toilet bar is based on mild synthetic surfactants as disclosed in US-A-4,673,525, Small et al., issued June 16, 1987.
- Synthetic detergents can also be present in compositions herein.
- Preferred types of synthetic detergents are of the anionic or nonionic type.
- anionic synthetic detergents are the salts of organic sulfuric reaction products such as
- R24 is a straight or branched chain alkyl of from 8 to 24 carbon atoms; M is an alkali metal or ammonium ion; x is a number of from 1 to 10; y is a number of from 1 to 4; and X is selected from the group consisting of chlorine, hydroxyl, and -SO3M, at least one X in each molecule being -SO3M.
- nonionic synthetic detergents are ethoxylated fatty alcohols (e.g., the reaction product of one mole of coconut fatty alcohol with from 3 to 30 moles of ethylene oxide) and fatty acid amides such as coconut fatty acid monoethanolamide and stearic acid diethanolamide.
- compositions herein can be free of synthetic detergents.
- synthetic detergents include the mild synthetic surfactants disclosed in US-A-4,673,525, Small et al., issued June 16, 1987.
- Insoluble alkaline earth metal soaps such as calcium stearate and magnesium stearate can also be incorporated into compositions of the present invention at levels up to 30% by weight. These materials are particularly useful in toilet bars in which synthetic detergents are present in that they tend to reduce the relatively high solubility which such bars normally have. These alkaline earth metal soaps are not included within the term “soap” as otherwise used in this specification.
- the term “soap” as used herein refers to the alkali metal soaps.
- compositions of the present invention can contain optional components such as those conventionally found in personal cleansing products.
- Conventional antibacterial agents can be included in the present compositions at levels of from 0.5% to 4% by weight.
- Typical antibacterial agents which are suitable for use herein are 3,4-di- and 3,4',5-tribromosalicylanilides; 4,4'-dichloro-3-(trifluoromethyl)carbanilide; 3,4,4'-trichlorocarbanilide and mixtures of these materials.
- Conventional nonionic emollients can be included as additional skin conditioning agents in the compositions of the present invention at levels up to 40%, preferably at levels of from 1% to 25% by weight.
- Such materials include, for example mineral oils, paraffin wax having a melting point of from about 37.8°C (about 100°F.), fatty sorbitan esters (see US-A-3,988,255, Seiden, issued Oct. 26, 1976 , lanolin and lanolin derivatives, esters such as isopropyl myristate and triglycerides such as coconut oil or hydrogenated tallow.
- Free fatty acid such as coconut fatty acid can be added to the compositions herein to improve the volume and quality (creaminess) of the lather produced by the compositions herein.
- perfumes, dyes and pigments can also be incorporated into compositions of the invention at levels up to 5% by weight.
- Perfumes are preferably used at levels of from 0.5% to 3% by weight and dyes and pigments are preferably used at levels of from 0.001% to 0.5% by weight.
- Toilet bars of the present invention can be prepared in any conventional manner.
- the bulky amine cationic polymer can be added to noodles of the base soap mixture containing from 10% to 22% moisture in an amalgamator. Any optional ingredients such as perfumes, dyes, etc., are also added to the amalgamator.
- the mixture is processed in the amalgamator and milled in the conventional manner under conventional conditions. It is then extruded (plodded) into logs for cutting and stamping into toilet bars.
- the bulky amine cationic polymer is added to soap noodle and mixed in the soap mixing steps of the soap bar making process.
- the soap bars of this invention contain up to 15% by weight of a synthetic surfactant. If a synthetic surfactant is included, a mild one is preferred.
- a mild synthetic surfactant is defined herein as one which does relatively little damage to the barrier function of the stratum corneum.
- the mild surfactant is preferably used at a level of 2-15% by weight.
- the fatty acid soap and mild surfactant mixture preferably has a ratio of 2.5:1 to 37:1, preferably from 2.5:1 to 14:1, and most preferably from 6.5:1 to 14:1, soap:synthetic.
- a preferred soap bar of this invention also contains from 2% to 17% by weight moisturizer, preferably one selected from glycerin and free fatty acid or mixtures thereof.
- the more preferred bar of this invention contains at least 4% by weight moisturizer.
- Some preferred mild synthetic surfactants useful in this invention include alkyl glyceryl ether sulfonate (AGS), anionic acyl sarcosinates, methyl acyl taurates, N-acyl glutamates, alkyl glucosides, acyl isethionates, alkyl sulfosuccinate, alkyl phosphate esters, ethoxylated alkyl phosphate esters, alkyl ether sulfates, methyl glucose esters, protein condensates, mixtures of alkyl ether sulfates and alkyl amine oxides, betaines, sultaines, and mixtures thereof.
- AGS alkyl glyceryl ether sulfonate
- anionic acyl sarcosinates methyl acyl taurates
- N-acyl glutamates N-acyl glutamates
- alkyl glucosides acyl isethionates
- alkyl ether sulfates with 1 to 12 ethoxy groups especially ammonium and sodium lauryl ether sulfates.
- Alkyl chain lengths for these surfactants are C8-C22, preferably C10-C18.
- the most preferred mild surfactant is sodium CN AGS.
- Plodded soap noodles are conveyed to a continuous mixer (CM) where approximately 1.0 part of cationic polymer is introduced, mixed, and plodded with the soap noodles. Uniform distribution during this addition and mixing step is important for acceptable bar feel performance.
- the polymer/soap noodles (generic noodles) are conveyed to milling.
- Two four-roll soap mills feed, stationary, middle, and top rolls are used in this step. This is a split milling (two set of mills are used in parallel) process to obtain a homogeneous mix. Efficient milling is needed in this intimate mixing step.
- CM continuous mixer
- CM wet mixing
- the mixture is milled using a four-roll mill, plodded, and then stamped into toilet bars of any convenient size and shape.
- the resulting bars are tested for odor.
- the bars have a pH of 9.5 in a 1% aqueous solution.
- the pH buffers are commercially available buffers:
- JR-400 made by Union Carbide Corporation and JAGUAR C-15 (RTM) made by Hi-Tek Polymers, Inc., are outside the selected polymers of this invention.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Emergency Medicine (AREA)
- Detergent Compositions (AREA)
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Claims (8)
- Composition pour le nettoyage corporel, sous la forme d'un pain de toilette comprenant de 5 à 90 % en poids d'un tensioactif choisi parmi les savons de métal alcalin et les mélanges de savons de métal alcalin et de tensioactifs synthétiques, le tensioactif synthétique étant présent en une quantité allant jusqu'à 15 % en poids ; et de 0,2 à 5 % en poids d'un polymère cationique quaternisé dans lequel chaque fragment ammonium a la formule :
-CR¹H-CRR³-NR⁴R⁵R⁶
dans laquelle R¹ à R³ sont H ou un autre substituant quelconque et au moins l'un des groupes R⁴, R⁵ et R⁶ est un groupe alkyle ayant de 2 à 24 atomes de carbone, un groupe alcoxyalkyle contenant de 2 à 12 atomes de carbone ou un groupe hydroxyéthyle ; et où chaque fragment ammonium quaternaire dérive d'une amine volumineuse ayant un point d'ébullition supérieur à 80°C, grâce à quoi le polymère cationique est pratiquement exempt de groupes formant des amines odoriférantes dans un environnement basique ;
et dans laquelle ladite composition a un pH d'au moins 8,5 en solution aqueuse à 1 %. - Composition pour le nettoyage corporel selon la revendication 1, dans laquelle ledit polymère cationique est une gomme de guar cationique.
- Composition pour le nettoyage corporel selon la revendication 1, dans laquelle ledit polymère cationique est présent à raison de 0,5 à 4 % en poids.
- Composition pour le nettoyage corporel selon la revendication 1, dans laquelle ledit polymère cationique a une masse moléculaire comprise entre 1.000 et 3.000.000 et est choisi dans l'ensemble constitué par :i) les polysaccharides cationiques ;ii) les copolymères cationiques de saccharides et de monomères cationiques synthétiques ; etiii) les polymères synthétiques choisis dans l'ensemble constitué par :a) les silicones quaternisées,b) les méthacrylates quaternisés ; etiv) leurs mélanges.
- Procédé pour préparer la composition pour le nettoyage corporel conforme à la revendication 1, comprenant les étapes consistant à :a) former un mélange dudit polymère cationique et desdites nouilles de mélange de savons de métal alcalin, dans lequel ledit polymère est présent dans ledit mélange en une quantité suffisante pour que le polymère représente de 0,2 à 5 % en poids de ladite composition ; ledit mélange contenant de 6 à 15 % d'humidité ;b) broyer ledit mélange en un mélange uniforme ;c) boudiner ledit'mélange uniforme ;d) extruder ledit mélange broyé et boudiné ; ete) emboutir ledit mélange extrudé en pains de toilette.
- Composition pour le nettoyage corporel selon la revendication 1, dans laquelle ladite composition contient de 2 à 15 % en poids d'un tensioactif synthétique choisi parmi les alkylglycéryléthersulfonates, les acylsarcosinates anioniques, les méthylacyltaurates, les N-acylglutamates, les alkylglucosides, les acyliséthionates, les alkylsulfosuccinates, les esters alkylphosphates, les esters alkylphosphates éthoxylés, les esters méthyl-glucose, les produits de condensation protéiniques, les mélanges d'alkylsulfates éthoxylés et d'oxydes d'alkylamines, les bétaïnes, les sultaïnes, les alkylsulfates éthoxylés ayant de 1 à 12 groupes éthoxy, et leurs mélanges, dans laquelle ledit tensioactif synthétique contient des chaînes alkyle contenant de 8 à 22 atomes de carbone.
- Procédé selon la revendication 7, dans lequel ladite composition contient de 5 à 10 % en poids d'un (alkyl en C₈-C₁₈)glycéryléthersulfonates.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US374315 | 1982-05-03 | ||
US37431589A | 1989-06-30 | 1989-06-30 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0405664A2 EP0405664A2 (fr) | 1991-01-02 |
EP0405664A3 EP0405664A3 (fr) | 1991-01-16 |
EP0405664B1 true EP0405664B1 (fr) | 1996-04-24 |
Family
ID=23476241
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP90201638A Expired - Lifetime EP0405664B1 (fr) | 1989-06-30 | 1990-06-22 | Produit pour le nettoyage corporel avec polymère cationique à groupe amine encombrante et odeur compatible |
Country Status (18)
Country | Link |
---|---|
EP (1) | EP0405664B1 (fr) |
JP (1) | JP2930671B2 (fr) |
AR (1) | AR243596A1 (fr) |
AT (1) | ATE137260T1 (fr) |
AU (1) | AU620999B2 (fr) |
BR (1) | BR9003038A (fr) |
CA (1) | CA2019264C (fr) |
DE (1) | DE69026651T2 (fr) |
DK (1) | DK0405664T3 (fr) |
EG (1) | EG19777A (fr) |
ES (1) | ES2086362T3 (fr) |
GR (1) | GR3019754T3 (fr) |
MA (1) | MA21897A1 (fr) |
MX (1) | MX173483B (fr) |
MY (1) | MY107250A (fr) |
NZ (1) | NZ234293A (fr) |
PE (1) | PE13191A1 (fr) |
TR (1) | TR24531A (fr) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5154849A (en) * | 1990-11-16 | 1992-10-13 | The Procter & Gamble Company | Mild skin cleansing toilet bar with silicone skin mildness/moisturizing aid |
US5387675A (en) * | 1993-03-10 | 1995-02-07 | Rhone-Poulenc Specialty Chemicals Co. | Modified hydrophobic cationic thickening compositions |
US5849280A (en) † | 1996-08-06 | 1998-12-15 | A-Veda Corporation | Hair conditioning solid |
US5858939A (en) * | 1997-03-21 | 1999-01-12 | Lever Brothers Company, Division Of Conopco, Inc. | Method for preparing bars comprising use of separate bar adjuvant compositions comprising benefit agent and deposition polymer |
ES2379799T3 (es) * | 2004-08-31 | 2012-05-03 | Hercules Incorporated | Procedimiento para preparar poligalactomanano catiónico de bajo peso molecular con olor reducido |
IT1391979B1 (it) * | 2008-07-18 | 2012-02-02 | Lamberti Spa | Eteri di galattomannani modificati |
JP5367494B2 (ja) * | 2009-08-06 | 2013-12-11 | 花王株式会社 | 枠練り石鹸の製造方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0308189A2 (fr) * | 1987-09-17 | 1989-03-22 | The Procter & Gamble Company | Pain de toilette nettoyant à basse teneur d'humidité |
EP0337354A1 (fr) * | 1988-04-12 | 1989-10-18 | Kao Corporation | Composition détergente faiblement irritante |
WO1990015589A1 (fr) * | 1989-06-16 | 1990-12-27 | Wella Aktiengesellschaft | Produit translucide pour les soins du corps et des cheveux |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3761418A (en) * | 1967-09-27 | 1973-09-25 | Procter & Gamble | Detergent compositions containing particle deposition enhancing agents |
US4061602A (en) * | 1976-08-03 | 1977-12-06 | American Cyanamid Company | Conditioning shampoo composition containing a cationic derivative of a natural gum (such as guar) as the active conditioning ingredient |
US4234464A (en) * | 1979-04-09 | 1980-11-18 | Gaf Corporation | Detergent bar composition and binder therefor |
US4948576A (en) * | 1983-02-18 | 1990-08-14 | Johnson & Johnson Consumer Products, Inc. | Detergent compositions |
CA2001314C (fr) * | 1988-11-02 | 1995-05-09 | John Robert Knochel | Compose pour pains de savon de toilette a base de gomme de guar cationique |
-
1990
- 1990-06-19 CA CA002019264A patent/CA2019264C/fr not_active Expired - Fee Related
- 1990-06-22 EP EP90201638A patent/EP0405664B1/fr not_active Expired - Lifetime
- 1990-06-22 ES ES90201638T patent/ES2086362T3/es not_active Expired - Lifetime
- 1990-06-22 DE DE69026651T patent/DE69026651T2/de not_active Expired - Fee Related
- 1990-06-22 DK DK90201638.5T patent/DK0405664T3/da active
- 1990-06-22 AT AT90201638T patent/ATE137260T1/de not_active IP Right Cessation
- 1990-06-25 TR TR90/0575A patent/TR24531A/xx unknown
- 1990-06-26 PE PE1990171296A patent/PE13191A1/es unknown
- 1990-06-27 AR AR90317240A patent/AR243596A1/es active
- 1990-06-28 EG EG40090A patent/EG19777A/xx active
- 1990-06-28 NZ NZ234293A patent/NZ234293A/en unknown
- 1990-06-28 MY MYPI90001099A patent/MY107250A/en unknown
- 1990-06-29 MX MX021383A patent/MX173483B/es unknown
- 1990-06-29 BR BR909003038A patent/BR9003038A/pt not_active IP Right Cessation
- 1990-06-29 AU AU58055/90A patent/AU620999B2/en not_active Ceased
- 1990-06-30 JP JP2174349A patent/JP2930671B2/ja not_active Expired - Lifetime
- 1990-07-02 MA MA22166A patent/MA21897A1/fr unknown
-
1996
- 1996-04-25 GR GR950403556T patent/GR3019754T3/el unknown
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0308189A2 (fr) * | 1987-09-17 | 1989-03-22 | The Procter & Gamble Company | Pain de toilette nettoyant à basse teneur d'humidité |
EP0337354A1 (fr) * | 1988-04-12 | 1989-10-18 | Kao Corporation | Composition détergente faiblement irritante |
WO1990015589A1 (fr) * | 1989-06-16 | 1990-12-27 | Wella Aktiengesellschaft | Produit translucide pour les soins du corps et des cheveux |
Also Published As
Publication number | Publication date |
---|---|
ES2086362T3 (es) | 1996-07-01 |
ATE137260T1 (de) | 1996-05-15 |
CA2019264C (fr) | 1995-07-18 |
MX173483B (es) | 1994-03-08 |
PE13191A1 (es) | 1991-04-05 |
NZ234293A (en) | 1993-08-26 |
MY107250A (en) | 1995-10-31 |
MA21897A1 (fr) | 1991-04-01 |
JPH03115210A (ja) | 1991-05-16 |
AU620999B2 (en) | 1992-02-27 |
GR3019754T3 (en) | 1996-07-31 |
JP2930671B2 (ja) | 1999-08-03 |
EP0405664A3 (fr) | 1991-01-16 |
CA2019264A1 (fr) | 1990-12-31 |
TR24531A (tr) | 1991-11-01 |
EP0405664A2 (fr) | 1991-01-02 |
EG19777A (en) | 1996-03-31 |
AU5805590A (en) | 1991-01-03 |
DE69026651T2 (de) | 1996-11-21 |
DE69026651D1 (de) | 1996-05-30 |
AR243596A1 (es) | 1993-08-31 |
DK0405664T3 (da) | 1996-08-12 |
BR9003038A (pt) | 1991-08-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5202048A (en) | Personal cleansing product with odor compatible bulky amine cationic polymer with reduced odor characteristics | |
US4946618A (en) | Toilet bar composition containing cationic guar gum | |
US4704224A (en) | Soap bar composition containing guar gum | |
US5154849A (en) | Mild skin cleansing toilet bar with silicone skin mildness/moisturizing aid | |
AU605750B2 (en) | Toilet soap composition | |
US5264144A (en) | Freezer personal cleansing bar with selected fatty acid soaps for improved mildness and good lather | |
EP0308190B1 (fr) | Pain de toilette nettoyant ultradoux avec un mélange de polymères sélectionnés | |
US5076953A (en) | Skin cleansing synbars with low moisture and/or selected polymeric skin mildness aids | |
EP0308189B1 (fr) | Pain de toilette nettoyant à basse teneur d'humidité | |
DE69817789T2 (de) | Körperreinigungsmittelstuck mit verbesserter absetzung | |
DE69813865T2 (de) | Stückförmige zusammensetzung mit dispergieten tröpfchen eines aufweichmittels | |
KR100453672B1 (ko) | 폴리알킬렌글리콜의블렌드를함유하는마일드바아조성물 | |
EP0759971B1 (fr) | Pain de savon de toilette doux contenant de tres petites particules de cire | |
EP0367335B1 (fr) | Composition de barre de toilette contenant une gomme de guar cationique | |
EP0405664B1 (fr) | Produit pour le nettoyage corporel avec polymère cationique à groupe amine encombrante et odeur compatible | |
RU2294960C2 (ru) | Композиция бруска моющего средства, содержащего анионное поверхностно-активное вещество, мыло, соль, гидроксикислоты и наполнитель | |
AU2960797A (en) | Bar composition comprising copolymer mildness actives | |
JP2592547B2 (ja) | 洗剤組成物 | |
AU609423B2 (en) | Soap composition | |
CA2524933C (fr) | Composition de savon liquide transparent | |
US5021183A (en) | Soap composition | |
AU1795497A (en) | Bar composition comprising copolymer mildness actives | |
WO1994019442A1 (fr) | Composition de toilette | |
NZ248471A (en) | A "freezer" soap bar comprising mostly na and k soaps of: myristic, palmitic and stearic acids plus oleic and/or lauric acid and/or minor fatty acid soap; water; and optionally a lathering synthetic surfactant and a sugar |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU NL SE |
|
AK | Designated contracting states |
Kind code of ref document: A3 Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU NL SE |
|
17P | Request for examination filed |
Effective date: 19910710 |
|
17Q | First examination report despatched |
Effective date: 19940520 |
|
17Q | First examination report despatched |
Effective date: 19950502 |
|
GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU NL SE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 19960424 |
|
REF | Corresponds to: |
Ref document number: 137260 Country of ref document: AT Date of ref document: 19960515 Kind code of ref document: T |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: NV Representative=s name: RITSCHER & SEIFERT PATENTANWAELTE VSP |
|
REF | Corresponds to: |
Ref document number: 69026651 Country of ref document: DE Date of ref document: 19960530 |
|
ET | Fr: translation filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DK Payment date: 19960607 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: AT Payment date: 19960612 Year of fee payment: 7 |
|
ITF | It: translation for a ep patent filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 19960619 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 19960626 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 19960627 Year of fee payment: 7 |
|
REG | Reference to a national code |
Ref country code: GR Ref legal event code: FG4A Free format text: 3019754 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: LU Payment date: 19960701 Year of fee payment: 7 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2086362 Country of ref document: ES Kind code of ref document: T3 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 19960704 Year of fee payment: 7 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Effective date: 19960724 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 19960812 Year of fee payment: 7 |
|
REG | Reference to a national code |
Ref country code: DK Ref legal event code: T3 |
|
NLV1 | Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act | ||
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19970622 Ref country code: DK Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19970622 Ref country code: AT Effective date: 19970622 |
|
REG | Reference to a national code |
Ref country code: DK Ref legal event code: EBP |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 19970623 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19970630 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19970630 Ref country code: BE Effective date: 19970630 |
|
BERE | Be: lapsed |
Owner name: THE PROCTER & GAMBLE CY Effective date: 19970630 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20000301 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GR Payment date: 20010420 Year of fee payment: 12 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20020501 Year of fee payment: 13 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20020605 Year of fee payment: 13 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20020628 Year of fee payment: 13 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20021231 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20030622 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20040101 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20030622 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20040227 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED. Effective date: 20050622 |