LU87534A1 - Compositions cosmetiques contenant un agent epaississant un polymere ayant une faible proportion de motifs a groupements ioniques - Google Patents

Compositions cosmetiques contenant un agent epaississant un polymere ayant une faible proportion de motifs a groupements ioniques Download PDF

Info

Publication number: LU87534A1
Authority: LU; Luxembourg
Prior art keywords: composition; units; support according; formula; copolymer
Prior art date: 1989-06-09

Application number

LU87534A

Other languages

English (en)

French (fr)

Inventor

Mondet Jean

Papantoniou Christos

Vanlerberghe Guy

Original Assignee

Oreal

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

1989-06-09

Filing date

1989-06-09

Publication date

1991-02-18

1989-06-09 Application filed by Oreal filed Critical Oreal

1989-06-09 Priority to LU87534A priority Critical patent/LU87534A1/fr

1990-06-08 Priority to US07/535,204 priority patent/US5318995A/en

1990-06-08 Priority to CA002018628A priority patent/CA2018628A1/fr

1990-06-08 Priority to AT90401575T priority patent/ATE116538T1/de

1990-06-08 Priority to EP90401575A priority patent/EP0406042B1/fr

1990-06-08 Priority to DE69015711T priority patent/DE69015711T2/de

1990-06-08 Priority to ES90401575T priority patent/ES2067705T3/es

1990-06-11 Priority to JP2152483A priority patent/JP2753763B2/ja

1991-02-18 Publication of LU87534A1 publication Critical patent/LU87534A1/fr

Links

239000000203 mixture Substances 0.000 title claims abstract description 48
239000002537 cosmetic Substances 0.000 title claims abstract description 22
239000002562 thickening agent Substances 0.000 title claims abstract description 10
229920000642 polymer Polymers 0.000 title description 23
229920001577 copolymer Polymers 0.000 claims abstract description 30
239000000839 emulsion Substances 0.000 claims abstract description 22
229930195734 saturated hydrocarbon Natural products 0.000 claims abstract description 9
125000004430 oxygen atom Chemical group O* 0.000 claims abstract description 5
125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 20
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 15
-1 2-ethylhexyl Chemical group 0.000 claims description 12
125000004432 carbon atom Chemical group C* 0.000 claims description 11
150000003839 salts Chemical class 0.000 claims description 10
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 8
239000000178 monomer Substances 0.000 claims description 8
229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 claims description 7
XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 claims description 6
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 6
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 6
239000006184 cosolvent Substances 0.000 claims description 6
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical class CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 5
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 5
229910052751 metal Inorganic materials 0.000 claims description 4
239000002184 metal Substances 0.000 claims description 4
238000002360 preparation method Methods 0.000 claims description 4
PRAMZQXXPOLCIY-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethanesulfonic acid Chemical compound CC(=C)C(=O)OCCS(O)(=O)=O PRAMZQXXPOLCIY-UHFFFAOYSA-N 0.000 claims description 3
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
150000003926 acrylamides Chemical class 0.000 claims description 3
229910052725 zinc Chemical class 0.000 claims description 3
239000011701 zinc Chemical class 0.000 claims description 3
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 2
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 claims description 2
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
150000001252 acrylic acid derivatives Chemical class 0.000 claims description 2
229910052783 alkali metal Inorganic materials 0.000 claims description 2
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
229910052744 lithium Inorganic materials 0.000 claims description 2
150000002734 metacrylic acid derivatives Chemical class 0.000 claims description 2
229910052700 potassium Inorganic materials 0.000 claims description 2
239000011591 potassium Substances 0.000 claims description 2
UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 claims description 2
229910052708 sodium Inorganic materials 0.000 claims description 2
239000011734 sodium Substances 0.000 claims description 2
230000007928 solubilization Effects 0.000 claims description 2
238000005063 solubilization Methods 0.000 claims description 2
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 claims description 2
BCRQXZHHCHBQRT-UHFFFAOYSA-N CCCCCCCCCC(=O)OCCS(O)(=O)=O Chemical compound CCCCCCCCCC(=O)OCCS(O)(=O)=O BCRQXZHHCHBQRT-UHFFFAOYSA-N 0.000 claims 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims 1
125000003158 alcohol group Chemical group 0.000 claims 1
150000001340 alkali metals Chemical class 0.000 claims 1
150000001342 alkaline earth metals Chemical class 0.000 claims 1
229910052791 calcium Inorganic materials 0.000 claims 1
239000011575 calcium Substances 0.000 claims 1
125000005842 heteroatom Chemical group 0.000 claims 1
159000000003 magnesium salts Chemical class 0.000 claims 1
FRPDUHFLNQULDW-UHFFFAOYSA-N n-butyl-n-dodecylprop-2-enamide Chemical compound CCCCCCCCCCCCN(C(=O)C=C)CCCC FRPDUHFLNQULDW-UHFFFAOYSA-N 0.000 claims 1
CKZGUNURVPANST-UHFFFAOYSA-N n-dodecyl-n-ethylprop-2-enamide Chemical compound CCCCCCCCCCCCN(CC)C(=O)C=C CKZGUNURVPANST-UHFFFAOYSA-N 0.000 claims 1
230000001737 promoting effect Effects 0.000 claims 1
229920006395 saturated elastomer Polymers 0.000 claims 1
229910006069 SO3H Inorganic materials 0.000 abstract 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
239000005864 Sulphur Substances 0.000 abstract 1
150000001408 amides Chemical class 0.000 abstract 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
150000002148 esters Chemical class 0.000 abstract 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 30
239000000243 solution Substances 0.000 description 30
238000003756 stirring Methods 0.000 description 27
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
229910052757 nitrogen Inorganic materials 0.000 description 16
239000003921 oil Substances 0.000 description 14
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 12
230000005587 bubbling Effects 0.000 description 12
238000006386 neutralization reaction Methods 0.000 description 11
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
239000002253 acid Substances 0.000 description 9
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
235000019198 oils Nutrition 0.000 description 8
239000012071 phase Substances 0.000 description 7
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
238000004458 analytical method Methods 0.000 description 6
239000006071 cream Substances 0.000 description 6
239000003999 initiator Substances 0.000 description 6
238000000034 method Methods 0.000 description 6
239000002244 precipitate Substances 0.000 description 6
238000001556 precipitation Methods 0.000 description 6
159000000000 sodium salts Chemical class 0.000 description 6
239000003995 emulsifying agent Substances 0.000 description 5
150000002430 hydrocarbons Chemical group 0.000 description 5
238000010907 mechanical stirring Methods 0.000 description 5
230000008719 thickening Effects 0.000 description 5
238000007334 copolymerization reaction Methods 0.000 description 4
239000008367 deionised water Substances 0.000 description 4
229910021641 deionized water Inorganic materials 0.000 description 4
238000004090 dissolution Methods 0.000 description 4
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 4
229910052753 mercury Inorganic materials 0.000 description 4
238000006116 polymerization reaction Methods 0.000 description 4
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
239000008346 aqueous phase Substances 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
238000001035 drying Methods 0.000 description 3
239000012429 reaction media Substances 0.000 description 3
XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical group CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
GASMGDMKGYYAHY-UHFFFAOYSA-N 2-methylidenehexanamide Chemical compound CCCCC(=C)C(N)=O GASMGDMKGYYAHY-UHFFFAOYSA-N 0.000 description 2
UHQADSBKMJUJEK-UHFFFAOYSA-N 2-methylidenetetradecanamide Chemical compound CCCCCCCCCCCCC(=C)C(N)=O UHQADSBKMJUJEK-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
DLAHAXOYRFRPFQ-UHFFFAOYSA-N dodecyl benzoate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=CC=C1 DLAHAXOYRFRPFQ-UHFFFAOYSA-N 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
230000008020 evaporation Effects 0.000 description 2
238000011065 in-situ storage Methods 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
125000003010 ionic group Chemical group 0.000 description 2
210000004080 milk Anatomy 0.000 description 2
235000013336 milk Nutrition 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000012074 organic phase Substances 0.000 description 2
229920000223 polyglycerol Polymers 0.000 description 2
239000002904 solvent Substances 0.000 description 2
238000006277 sulfonation reaction Methods 0.000 description 2
125000000542 sulfonic acid group Chemical group 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
239000001993 wax Substances 0.000 description 2
239000004246 zinc acetate Substances 0.000 description 2
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 1
RUEOYQNDBAHZBS-UHFFFAOYSA-N 4-[2-hydroxy-3-(2-hydroxy-3-octadecanoyloxypropoxy)propoxy]-4-oxobutanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)COCC(O)COC(=O)CCC(O)=O RUEOYQNDBAHZBS-UHFFFAOYSA-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
RGCKGOZRHPZPFP-UHFFFAOYSA-N Alizarin Natural products C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
239000005662 Paraffin oil Substances 0.000 description 1
229920002367 Polyisobutene Polymers 0.000 description 1
235000019486 Sunflower oil Nutrition 0.000 description 1
LDKDGDIWEUUXSH-UHFFFAOYSA-N Thymophthalein Chemical compound C1=C(O)C(C(C)C)=CC(C2(C3=CC=CC=C3C(=O)O2)C=2C(=CC(O)=C(C(C)C)C=2)C)=C1C LDKDGDIWEUUXSH-UHFFFAOYSA-N 0.000 description 1
235000018936 Vitellaria paradoxa Nutrition 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000000470 constituent Substances 0.000 description 1
GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 1
150000004683 dihydrates Chemical class 0.000 description 1
238000007865 diluting Methods 0.000 description 1
238000004821 distillation Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000007701 flash-distillation Methods 0.000 description 1
239000012530 fluid Substances 0.000 description 1
238000004108 freeze drying Methods 0.000 description 1
125000005456 glyceride group Chemical group 0.000 description 1
238000000227 grinding Methods 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
229920006007 hydrogenated polyisobutylene Polymers 0.000 description 1
239000005457 ice water Substances 0.000 description 1
ASKIVFGGGGIGKH-UHFFFAOYSA-N isostearic acid monoglyceride Natural products CC(C)CCCCCCCCCCCCCCC(=O)OCC(O)CO ASKIVFGGGGIGKH-UHFFFAOYSA-N 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
XQPVIMDDIXCFFS-UHFFFAOYSA-N n-dodecylprop-2-enamide Chemical compound CCCCCCCCCCCCNC(=O)C=C XQPVIMDDIXCFFS-UHFFFAOYSA-N 0.000 description 1
CNWVYEGPPMQTKA-UHFFFAOYSA-N n-octadecylprop-2-enamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)C=C CNWVYEGPPMQTKA-UHFFFAOYSA-N 0.000 description 1
XFHJDMUEHUHAJW-UHFFFAOYSA-N n-tert-butylprop-2-enamide Chemical compound CC(C)(C)NC(=O)C=C XFHJDMUEHUHAJW-UHFFFAOYSA-N 0.000 description 1
HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
239000002304 perfume Substances 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
238000004313 potentiometry Methods 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
239000002600 sunflower oil Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
150000003626 triacylglycerols Chemical class 0.000 description 1
238000007738 vacuum evaporation Methods 0.000 description 1
239000007762 w/o emulsion Substances 0.000 description 1
150000003751 zinc Chemical class 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
- A61K8/064—Water-in-oil emulsions, e.g. Water-in-silicone emulsions
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8158—Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; Compositions of derivatives of such polymers
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
General Health & Medical Sciences (AREA)
Birds (AREA)
Epidemiology (AREA)
Chemical & Material Sciences (AREA)
Dispersion Chemistry (AREA)
Oil, Petroleum & Natural Gas (AREA)
Dermatology (AREA)
Cosmetics (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Colloid Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

LU87534A 1989-06-09 1989-06-09 Compositions cosmetiques contenant un agent epaississant un polymere ayant une faible proportion de motifs a groupements ioniques LU87534A1 (fr)

Priority Applications (8)

Application Number	Priority Date	Filing Date	Title
LU87534A LU87534A1 (fr)	1989-06-09	1989-06-09	Compositions cosmetiques contenant un agent epaississant un polymere ayant une faible proportion de motifs a groupements ioniques
US07/535,204 US5318995A (en)	1989-06-09	1990-06-08	Cosmetic composition containing as a thickening agent a polymer having a slight proportion of units having ionic groups
CA002018628A CA2018628A1 (fr)	1989-06-09	1990-06-08	Compositions cosmetiques contenant comme agent epaississant un polymere ayant une faible proportion de motifs a groupements ioniques
AT90401575T ATE116538T1 (de)	1989-06-09	1990-06-08	Kosmetische mittel, die ein polymer mit niedrigem gehalt an einheiten mit ionischen substituenten als verdickungsmittel enthalten.
EP90401575A EP0406042B1 (fr)	1989-06-09	1990-06-08	Composition cosmétiques contenant comme agent épaississant un polymère ayant une faible proportion de motifs à groupements ioniques
DE69015711T DE69015711T2 (de)	1989-06-09	1990-06-08	Kosmetische Mittel, die ein Polymer mit niedrigem Gehalt an Einheiten mit ionischen Substituenten als Verdickungsmittel enthalten.
ES90401575T ES2067705T3 (es)	1989-06-09	1990-06-08	Composicion cosmetica que contiene como agente espesante un polimero que tiene una baja proporcion de motivos con grupos ionicos.
JP2152483A JP2753763B2 (ja)	1989-06-09	1990-06-11	低比率でイオン性基をもつ繰返し単位を有するポリマーを増粘剤として含有する化粧用組成物

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
LU87534		1989-06-09
LU87534A LU87534A1 (fr)	1989-06-09	1989-06-09	Compositions cosmetiques contenant un agent epaississant un polymere ayant une faible proportion de motifs a groupements ioniques

Publications (1)

Publication Number	Publication Date
LU87534A1 true LU87534A1 (fr)	1991-02-18

Family

ID=19731169

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU87534A LU87534A1 (fr)	1989-06-09	1989-06-09	Compositions cosmetiques contenant un agent epaississant un polymere ayant une faible proportion de motifs a groupements ioniques

Country Status (8)

Country	Link
US (1)	US5318995A (ja)
EP (1)	EP0406042B1 (ja)
JP (1)	JP2753763B2 (ja)
AT (1)	ATE116538T1 (ja)
CA (1)	CA2018628A1 (ja)
DE (1)	DE69015711T2 (ja)
ES (1)	ES2067705T3 (ja)
LU (1)	LU87534A1 (ja)

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FR2783159B1 (fr) *	1998-09-16	2000-11-17	Oreal	Emulsion comprenant un compose epaississant hydrophile et un copolymere epaississant, compositions comprenant ladite emulsion, et utilisations
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FR2818536A1 (fr) *	2000-12-22	2002-06-28	Oreal	Composition de teinture directe pour fibres keratiniques a base de polymeres amphiphiles d'au moins un monomere a insaturation ethylenique a groupement sulfonique et comportant une partie hydrophobe
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FR2819178B1 (fr) *	2001-01-11	2003-02-21	Oreal	Composition contenant au moins un compose insoluble dans l'eau particulier et au moins un polymere amphiphile
FR2819182B1 (fr) *	2001-01-11	2003-02-21	Oreal	Composition de nettoyage contenant un polymere amphiphile
FR2819184B1 (fr) *	2001-01-11	2003-02-21	Oreal	Composition stable a forte teneur en electrolyte, contenant un polymere amphiphile
FR2819179B1 (fr) *	2001-01-11	2003-02-21	Oreal	Compositions photoprotectrices a base de polymeres amphiphiles
FR2819175B1 (fr) *	2001-01-11	2003-02-21	Oreal	Composition cosmetique et/ou dermatologique acide contenant un polymere amphiphile
FR2819177B1 (fr) *	2001-01-11	2003-02-21	Oreal	Composition contenant au moins un agent conditionneur soluble particulier et au moins un polymere amphiphile
FR2819262B1 (fr) *	2001-01-11	2005-05-13	Oreal	Composition contenant au moins une silicone et au moins un polymere amphiphile
FR2819183B1 (fr) *	2001-01-11	2003-02-21	Oreal	Compositions autobronzantes a base de polymeres amphiphiles d'au moins un monomere a insaturation ethylenique a groupement sulfonique et comportant une partie hydrophobe
FR2824264B1 (fr) *	2001-05-04	2005-11-18	Oreal	Composition a phase grasse liquide gelifiee par un polymere semi-cristallin
US6951642B2 (en)	2001-09-28	2005-10-04	3M Innovative Properties Company	Water-in-oil emulsions with anionic groups, compositions, and methods
US7030203B2 (en)	2001-09-28	2006-04-18	3M Innovative Properties Company	Water-in-oil emulsions with ethylene oxide groups, compositions, and methods
FR2829142B1 (fr) *	2001-12-27	2004-02-13	Ulice	Composition filmogene d'heteroxylanes pour la fabrication de capsules ainsi obtenues
JP2005532994A (ja) *	2002-01-24	2005-11-04	ロレアル	半結晶性重合体およびエステルを含む組成物
ITVA20030002A1 (it) *	2003-01-09	2004-07-10	Lamberti Spa	Addensanti sintetici per cosmetici.
JP4538377B2 (ja) *	2005-06-03	2010-09-08	マルホ株式会社	油中水型乳化組成物
CN101442979B (zh) *	2006-05-11	2013-08-21	气体产品与化学公司	含有官能化聚合物的个人护理组合物
JP2010253406A (ja) *	2009-04-27	2010-11-11	Nof Corp	炭素材料用分散剤およびこれを含む組成物並びに分散液
US9233063B2 (en) *	2009-12-17	2016-01-12	Air Products And Chemicals, Inc.	Polymeric compositions for personal care products
FR2961210B1 (fr)	2010-06-15	2013-06-07	Soc Dexploitation De Produits Pour Les Industries Chimiques Seppic	Nouveaux polymeres epaississants des phases grasses
FR2961513B1 (fr)	2010-06-22	2012-07-13	Soc Dexploitation De Produits Pour Les Industries Chimiques Seppic	Nouveau polymere epaississant de phases grasses sans monomere ionique
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DE3732147A1 (de) *	1987-09-24	1989-04-06	Henkel Kgaa	Emulsionsfoermige wasserstoffperoxid-zubereitungen zum blondieren und oxidativen faerben der haare

1989
- 1989-06-09 LU LU87534A patent/LU87534A1/fr unknown
1990
- 1990-06-08 AT AT90401575T patent/ATE116538T1/de not_active IP Right Cessation
- 1990-06-08 EP EP90401575A patent/EP0406042B1/fr not_active Expired - Lifetime
- 1990-06-08 US US07/535,204 patent/US5318995A/en not_active Expired - Fee Related
- 1990-06-08 DE DE69015711T patent/DE69015711T2/de not_active Expired - Fee Related
- 1990-06-08 ES ES90401575T patent/ES2067705T3/es not_active Expired - Lifetime
- 1990-06-08 CA CA002018628A patent/CA2018628A1/fr not_active Abandoned
- 1990-06-11 JP JP2152483A patent/JP2753763B2/ja not_active Expired - Fee Related

Also Published As

Publication number	Publication date
CA2018628A1 (fr)	1990-12-09
JPH0379655A (ja)	1991-04-04
EP0406042B1 (fr)	1995-01-04
DE69015711D1 (de)	1995-02-16
JP2753763B2 (ja)	1998-05-20
ES2067705T3 (es)	1995-04-01
ATE116538T1 (de)	1995-01-15
EP0406042A2 (fr)	1991-01-02
DE69015711T2 (de)	1995-07-20
US5318995A (en)	1994-06-07
EP0406042A3 (en)	1991-02-06

Publication	Publication Date	Title
LU87534A1 (fr)	1991-02-18	Compositions cosmetiques contenant un agent epaississant un polymere ayant une faible proportion de motifs a groupements ioniques
EP0494022A1 (fr)	1992-07-08	Nouveaux copolymères à base de N-alkyl acrylamide, leur préparation et leur utilisation comme agents épaississants, notamment dans des compostions de shampooing
LU85789A1 (fr)	1986-09-02	Utilisation dans les domaines therapeutique et cosmetique d'une solution anhydre de peroxyde d'hydrogene
EP1743015A1 (fr)	2007-01-17	Composition tensioactive, procede de preparation et cosmetique comprenant cette composition
FR2614786A1 (fr)	1988-11-10	Compositions cosmetiques moussantes
FR2549826A1 (fr)	1985-02-01	Nouveaux ethers de polyols, leur procede de preparation et leur application en cosmetique
JP2976146B2 (ja)	1999-11-10	固形状組成物及びこれを含有する化粧料
CA2036402C (fr)	2003-01-07	Laque aerosol capillaire contenant un tetrapolymere d'acide acrylique, de n,n-dimethylacrylamide, de n-tertiobutylacrylamide et de methacrylate d'ethyle et un gaz propulseur non halogene
CA1182832A (fr)	1985-02-19	Oligomeres statistiques, tensio-actifs, procede pour les preparer et compositions les contenant
CA2115704A1 (fr)	1994-08-17	Fixatif sous forme de laque aqueuse en aerosol
JPS5914019B2 (ja)	1984-04-02	エステル化生成物及びこれらを含む化粧料
BE1004271A4 (fr)	1992-10-27	Compositions cosmetiques destinees a proteger la peau contre les effets indesires des radiations ultraviolettes.
EP1113029A1 (fr)	2001-07-04	Nouveaux polymères, le procédé pour leur préparation et les microlatex inverses les contenant
FR2830445A1 (fr)	2003-04-11	Utilisation d'alkylpolyxylosides comme agents ameliorant le toucher cosmetique d'emulsions huile-dans-eau contenant un polymere
JPS6241202B2 (ja)	1987-09-02
WO2011138534A1 (fr)	2011-11-10	Composition de dérivés polyalcoxylés de triméthylolpropane et d'alcools gras procédé pour sa préparation et utilisation comme inverseur, dans les latex inverses auto-inversibles
FR2703907A1 (fr)	1994-10-21	Composition cosmétique hydratante.
EP1448627B1 (fr)	2008-12-31	Polymere de tris(hydroxymethyl) acrylamidomethane, latex inverse et microlatex en contenant, utilisation desdits polymere, latex inverse et microlatex inverse
CA2304391A1 (fr)	2000-10-06	Composition cosmetique comprenant des polymeres ayant une structure en etoiles, lesdits polymeres et leur utilisation notamment en capillaire
EP2585504A1 (fr)	2013-05-01	Nouveau polymere epaississant de phases grasses sans monomere ionique
FR2670671A1 (fr)	1992-06-26	Laque aerosol pour la fixation des cheveux contenant un tetrapolymere d'acide acrylique, de n-vinylpyrrolidone, de n-tertiobutylacrylamide et de methacrylate d'ethyle.
FR2756830A1 (fr)	1998-06-12	Polymeres hydrophiles fluores
EP2582734A1 (fr)	2013-04-24	Nouveaux polymères épaississants de phases grasses
CH536822A (fr)	1973-06-29	Procédé de préparation de composés chimiques utilisables comme agents de surface non ioniques
JPH0374315A (ja)	1991-03-28	エステル化生成物及びこれを含有する化粧料又は外用剤