CA2304275C - Produit capillaire a base d'esters huiles a haute densite moleculaire - Google Patents

Produit capillaire a base d'esters huiles a haute densite moleculaire Download PDF

Info

Publication number: CA2304275C
Authority: CA; Canada
Prior art keywords: acid; hair; hair conditioning; molecular weight; conditioning composition
Prior art date: 1997-09-17
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 - Fee Related

Application number

CA002304275A

Other languages

English (en)

Other versions

CA2304275A1 (fr

Inventor

Hirotaka Uchiyama

Yukiko Mizoguchi

Arata Mitsumatsu

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

Procter and Gamble Co

Original Assignee

Procter and Gamble Co

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.)

1997-09-17

Filing date

1998-06-04

Publication date

2002-10-08

1997-09-17 Priority claimed from PCT/US1997/016403 external-priority patent/WO1999013824A1/fr

1997-11-12 Priority claimed from PCT/US1997/020736 external-priority patent/WO1999024014A1/fr

1998-06-04 Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co

1999-03-25 Publication of CA2304275A1 publication Critical patent/CA2304275A1/fr

2002-10-08 Application granted granted Critical

2002-10-08 Publication of CA2304275C publication Critical patent/CA2304275C/fr

2018-06-04 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

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UZBDLHYCYNXFRF-UHFFFAOYSA-N chloro(prop-1-enyl)silane Chemical class C(=CC)[SiH2]Cl UZBDLHYCYNXFRF-UHFFFAOYSA-N 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 description 1
SCXCDVTWABNWLW-UHFFFAOYSA-M decyl-dimethyl-octylazanium;chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCCCCCCC SCXCDVTWABNWLW-UHFFFAOYSA-M 0.000 description 1
230000008021 deposition Effects 0.000 description 1
VKKVMDHHSINGTJ-UHFFFAOYSA-M di(docosyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCCCCCC VKKVMDHHSINGTJ-UHFFFAOYSA-M 0.000 description 1
125000004985 dialkyl amino alkyl group Chemical group 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
OSSCGHSWPYDTQZ-UHFFFAOYSA-N diazanium hexadecanoate chloride Chemical compound [Cl-].[NH4+].C(CCCCCCCCCCCCC)CC(=O)[O-].[NH4+] OSSCGHSWPYDTQZ-UHFFFAOYSA-N 0.000 description 1
SWSFKKWJEHRFFP-UHFFFAOYSA-N dihexadecyl(dimethyl)azanium Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCC SWSFKKWJEHRFFP-UHFFFAOYSA-N 0.000 description 1
NAPSCFZYZVSQHF-UHFFFAOYSA-N dimantine Chemical compound CCCCCCCCCCCCCCCCCCN(C)C NAPSCFZYZVSQHF-UHFFFAOYSA-N 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
235000019301 disodium ethylene diamine tetraacetate Nutrition 0.000 description 1
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
IHDIFQKZWSOIBB-UHFFFAOYSA-M dodecyl-[(4-ethylphenyl)methyl]-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CC1=CC=C(CC)C=C1 IHDIFQKZWSOIBB-UHFFFAOYSA-M 0.000 description 1
GVKAQUUEBRPEMA-UHFFFAOYSA-N dotetracontan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCN GVKAQUUEBRPEMA-UHFFFAOYSA-N 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
230000002708 enhancing effect Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
DMMXZLMYEUEJFT-UHFFFAOYSA-N ethyl 16-methylheptadecanoate Chemical compound CCOC(=O)CCCCCCCCCCCCCCC(C)C DMMXZLMYEUEJFT-UHFFFAOYSA-N 0.000 description 1
FMMOOAYVCKXGMF-MURFETPASA-N ethyl linoleate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC FMMOOAYVCKXGMF-MURFETPASA-N 0.000 description 1
229940031016 ethyl linoleate Drugs 0.000 description 1
LVGKNOAMLMIIKO-QXMHVHEDSA-N ethyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC LVGKNOAMLMIIKO-QXMHVHEDSA-N 0.000 description 1
229940093471 ethyl oleate Drugs 0.000 description 1
125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
239000011521 glass Substances 0.000 description 1
150000004676 glycans Chemical class 0.000 description 1
229940074045 glyceryl distearate Drugs 0.000 description 1
229940075507 glyceryl monostearate Drugs 0.000 description 1
239000000665 guar gum Substances 0.000 description 1
235000010417 guar gum Nutrition 0.000 description 1
229960002154 guar gum Drugs 0.000 description 1
230000003760 hair shine Effects 0.000 description 1
230000003699 hair surface Effects 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical class C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 1
FPMPNVIMFPEKRN-UHFFFAOYSA-N hexyl 16-methylheptadecanoate Chemical compound CCCCCCOC(=O)CCCCCCCCCCCCCCC(C)C FPMPNVIMFPEKRN-UHFFFAOYSA-N 0.000 description 1
229940051250 hexylene glycol Drugs 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
NYMPGSQKHIOWIO-UHFFFAOYSA-N hydroxy(diphenyl)silicon Chemical class C=1C=CC=CC=1[Si](O)C1=CC=CC=C1 NYMPGSQKHIOWIO-UHFFFAOYSA-N 0.000 description 1
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
239000001863 hydroxypropyl cellulose Substances 0.000 description 1
235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
BUHXFUSLEBPCEB-UHFFFAOYSA-N icosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCN BUHXFUSLEBPCEB-UHFFFAOYSA-N 0.000 description 1
150000002460 imidazoles Chemical class 0.000 description 1
ZCTXEAQXZGPWFG-UHFFFAOYSA-N imidurea Chemical compound O=C1NC(=O)N(CO)C1NC(=O)NCNC(=O)NC1C(=O)NC(=O)N1CO ZCTXEAQXZGPWFG-UHFFFAOYSA-N 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
FMMOOAYVCKXGMF-UHFFFAOYSA-N linoleic acid ethyl ester Natural products CCCCCC=CCC=CCCCCCCCC(=O)OCC FMMOOAYVCKXGMF-UHFFFAOYSA-N 0.000 description 1
229960004488 linolenic acid Drugs 0.000 description 1
KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
239000004973 liquid crystal related substance Substances 0.000 description 1
TWXDDNPPQUTEOV-FVGYRXGTSA-N methamphetamine hydrochloride Chemical compound Cl.CN[C@@H](C)CC1=CC=CC=C1 TWXDDNPPQUTEOV-FVGYRXGTSA-N 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
229940073769 methyl oleate Drugs 0.000 description 1
239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
229960002216 methylparaben Drugs 0.000 description 1
238000002156 mixing Methods 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
235000019426 modified starch Nutrition 0.000 description 1
230000003020 moisturizing effect Effects 0.000 description 1
229940078812 myristyl myristate Drugs 0.000 description 1
229940049292 n-(3-(dimethylamino)propyl)octadecanamide Drugs 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
KHPAAXRLVYMUHU-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)NCCN(CC)CC KHPAAXRLVYMUHU-UHFFFAOYSA-N 0.000 description 1
UIUQXDQHAWBLOW-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]icosanamide Chemical compound CCCCCCCCCCCCCCCCCCCC(=O)NCCN(CC)CC UIUQXDQHAWBLOW-UHFFFAOYSA-N 0.000 description 1
NCBXVQKSCKRNTB-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]icosanamide Chemical compound CCCCCCCCCCCCCCCCCCCC(=O)NCCN(C)C NCBXVQKSCKRNTB-UHFFFAOYSA-N 0.000 description 1
XNJXGLWSAVUJRR-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCN(C)C XNJXGLWSAVUJRR-UHFFFAOYSA-N 0.000 description 1
DYAVLIWAWOZKBI-UHFFFAOYSA-N n-[3-(diethylamino)propyl]hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(=O)NCCCN(CC)CC DYAVLIWAWOZKBI-UHFFFAOYSA-N 0.000 description 1
KUIOQEAUQATWEY-UHFFFAOYSA-N n-[3-(diethylamino)propyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCCN(CC)CC KUIOQEAUQATWEY-UHFFFAOYSA-N 0.000 description 1
MNAZHGAWPCLLGX-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)NCCCN(C)C MNAZHGAWPCLLGX-UHFFFAOYSA-N 0.000 description 1
BDHJUCZXTYXGCZ-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(=O)NCCCN(C)C BDHJUCZXTYXGCZ-UHFFFAOYSA-N 0.000 description 1
HJXPIPGLPXVLGN-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]icosanamide Chemical compound CCCCCCCCCCCCCCCCCCCC(=O)NCCCN(C)C HJXPIPGLPXVLGN-UHFFFAOYSA-N 0.000 description 1
WWVIUVHFPSALDO-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCCN(C)C WWVIUVHFPSALDO-UHFFFAOYSA-N 0.000 description 1
WIBFFTLQMKKBLZ-SEYXRHQNSA-N n-butyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCCC WIBFFTLQMKKBLZ-SEYXRHQNSA-N 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
FBUKVWPVBMHYJY-UHFFFAOYSA-M nonanoate Chemical compound CCCCCCCCC([O-])=O FBUKVWPVBMHYJY-UHFFFAOYSA-M 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
NKBWPOSQERPBFI-UHFFFAOYSA-N octadecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC NKBWPOSQERPBFI-UHFFFAOYSA-N 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
BARWIPMJPCRCTP-UHFFFAOYSA-N oleic acid oleyl ester Natural products CCCCCCCCC=CCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC BARWIPMJPCRCTP-UHFFFAOYSA-N 0.000 description 1
229940099570 oleth-2 Drugs 0.000 description 1
BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
150000002916 oxazoles Chemical class 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000003002 pH adjusting agent Substances 0.000 description 1
LBIYNOAMNIKVKF-FPLPWBNLSA-N palmitoleyl alcohol Chemical compound CCCCCC\C=C/CCCCCCCCO LBIYNOAMNIKVKF-FPLPWBNLSA-N 0.000 description 1
125000000913 palmityl 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])[H] 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical class [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
239000000419 plant extract Substances 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
239000002861 polymer material Substances 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
150000004032 porphyrins Chemical class 0.000 description 1
235000011056 potassium acetate Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
UQPHTOCKKAJMRP-UHFFFAOYSA-N prop-2-enoic acid trimethyl-[3-(2-methylprop-2-enoylamino)propyl]azanium chloride Chemical compound [Cl-].C(C(=C)C)(=O)NCCC[N+](C)(C)C.C(C=C)(=O)O UQPHTOCKKAJMRP-UHFFFAOYSA-N 0.000 description 1
XEIOPEQGDSYOIH-MURFETPASA-N propan-2-yl (9z,12z)-octadeca-9,12-dienoate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OC(C)C XEIOPEQGDSYOIH-MURFETPASA-N 0.000 description 1
PZQSQRCNMZGWFT-QXMHVHEDSA-N propan-2-yl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC(C)C PZQSQRCNMZGWFT-QXMHVHEDSA-N 0.000 description 1
ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
229940093625 propylene glycol monostearate Drugs 0.000 description 1
229960003415 propylparaben Drugs 0.000 description 1
150000003219 pyrazolines Chemical class 0.000 description 1
150000003220 pyrenes Chemical class 0.000 description 1
AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 1
HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
229940089970 quaternium-14 Drugs 0.000 description 1
229940117359 quaternium-24 Drugs 0.000 description 1
229940079053 quaternium-27 Drugs 0.000 description 1
229940032043 quaternium-52 Drugs 0.000 description 1
229940073745 quaternium-82 Drugs 0.000 description 1
238000005956 quaternization reaction Methods 0.000 description 1
238000009877 rendering Methods 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
210000004761 scalp Anatomy 0.000 description 1
238000012216 screening Methods 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
239000010703 silicon Substances 0.000 description 1
150000003377 silicon compounds Chemical class 0.000 description 1
FDNAPBUWERUEDA-UHFFFAOYSA-N silicon tetrachloride Chemical compound Cl[Si](Cl)(Cl)Cl FDNAPBUWERUEDA-UHFFFAOYSA-N 0.000 description 1
229920005573 silicon-containing polymer Polymers 0.000 description 1
229920002379 silicone rubber Polymers 0.000 description 1
239000004945 silicone rubber Substances 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
239000001509 sodium citrate Substances 0.000 description 1
NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
239000002689 soil Substances 0.000 description 1
229950011392 sorbitan stearate Drugs 0.000 description 1
238000003892 spreading Methods 0.000 description 1
SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
229940032160 stearamidoethyl diethylamine Drugs 0.000 description 1
229940114926 stearate Drugs 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
238000010998 test method Methods 0.000 description 1
DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
ABVVEAHYODGCLZ-UHFFFAOYSA-N tridecan-1-amine Chemical compound CCCCCCCCCCCCCN ABVVEAHYODGCLZ-UHFFFAOYSA-N 0.000 description 1
UMQCZSNKDUWJRI-UHFFFAOYSA-M tris(2-hydroxyethyl)-octadecylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](CCO)(CCO)CCO UMQCZSNKDUWJRI-UHFFFAOYSA-M 0.000 description 1
GUIWIPNQQLZJIE-UHFFFAOYSA-K tris[2-(2-hydroxyethoxy)ethyl]-octadecylazanium;phosphate Chemical compound [O-]P([O-])([O-])=O.CCCCCCCCCCCCCCCCCC[N+](CCOCCO)(CCOCCO)CCOCCO GUIWIPNQQLZJIE-UHFFFAOYSA-K 0.000 description 1
KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
235000013343 vitamin Nutrition 0.000 description 1
239000011782 vitamin Substances 0.000 description 1
229930003231 vitamin Natural products 0.000 description 1
229940088594 vitamin Drugs 0.000 description 1
150000003722 vitamin derivatives Chemical class 0.000 description 1
PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/85—Polyesters
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
- 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
- A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/416—Quaternary ammonium compounds
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/42—Colour properties
- A61K2800/43—Pigments; Dyes
- A61K2800/434—Luminescent, Fluorescent; Optical brighteners; Photosensitizers

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Birds (AREA)
Epidemiology (AREA)
Dermatology (AREA)
Emergency Medicine (AREA)
Cosmetics (AREA)

CA002304275A 1997-09-17 1998-06-04 Produit capillaire a base d'esters huiles a haute densite moleculaire Expired - Fee Related CA2304275C (fr)

Applications Claiming Priority (5)

Application Number	Priority Date	Filing Date	Title
WOPCT/US97/16403		1997-09-17
PCT/US1997/016403 WO1999013824A1 (fr)	1997-09-17	1997-09-17	Compositions de soins capillaires comprenant des agents avivants a molecules de grande taille
PCT/US1997/020736 WO1999024014A1 (fr)	1997-11-12	1997-11-12	Compositions pour traitement capillaire comprenant des tensioactifs cationiques hydrophiliquement substitues et des composes a point de fusion eleve
WOPCT/US97/20736		1997-11-12
PCT/US1998/011781 WO1999013838A1 (fr)	1997-09-17	1998-06-04	Produit capillaire a base d'esters huiles

Publications (2)

Publication Number	Publication Date
CA2304275A1 CA2304275A1 (fr)	1999-03-25
CA2304275C true CA2304275C (fr)	2002-10-08

Family

ID=26792767

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA002304275A Expired - Fee Related CA2304275C (fr)	1997-09-17	1998-06-04	Produit capillaire a base d'esters huiles a haute densite moleculaire

Country Status (8)

Country	Link
EP (1)	EP1014919A1 (fr)
KR (1)	KR20010024125A (fr)
CN (1)	CN1279600A (fr)
BR (1)	BR9812347A (fr)
CA (1)	CA2304275C (fr)
NO (1)	NO20001352L (fr)
TR (1)	TR200001027T2 (fr)
WO (1)	WO1999013838A1 (fr)

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WO2000064412A1 (fr) *	1999-04-27	2000-11-02	The Procter & Gamble Company	Compositions d'apres-shampoing
AU5704899A (en) *	1999-09-03	2001-04-10	Procter & Gamble Company, The	A process for forming a hair care composition and a composition formed by same
MX234468B (es) *	2000-03-14	2006-02-15	Procter & Gamble	Composicion para el cuidado del cabello que contiene una polialquilenglicol (n) alquilamina.
JP2002293719A (ja) *	2001-03-29	2002-10-09	Asahi Denka Kogyo Kk	毛髪処理剤組成物
DE102008060147A1 (de) *	2008-12-03	2010-06-10	Henkel Ag & Co. Kgaa	Haarkonditionierende Mittel mit Imidazolinen und Esterölen
DE102009047528A1 (de) *	2009-12-04	2011-06-09	Henkel Ag & Co. Kgaa	Verwendung von Esteröl in Verfahren zur permanenten Haarumformung
CN104135991A (zh) *	2012-03-16	2014-11-05	莱雅公司	清洗角蛋白纤维的组合物
WO2017166088A1 (fr) *	2016-03-30	2017-10-05	Beiersdorf Daily Chemical (Wuhan) Co. Ltd.	Composition d'après-shampoing contenant un/des esters de pentaérythritol et un/des éthers alkyliques de ppg
MX2019013049A (es) *	2017-05-19	2019-12-11	Procter & Gamble	Composicion para el cuidado del cabello que comprende compuestos de tri-esteres y esteres grasos de acido benzoico.

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB9109734D0 (en) *	1991-05-07	1991-06-26	Unilever Plc	Cosmetic composition
DE4337169A1 (de) *	1993-10-30	1995-05-04	Hartmann Haarkosmetik Gmbh	Haarbehandlungsmittel, insbesondere zum Zwecke der Frisurengestaltung, das in Emulsionsform vorliegt und frei von haarfestigenden Polymeren bzw. Harzen ist
AU1410097A (en) *	1996-12-06	1998-06-29	Procter & Gamble Company, The	Hair conditioning compositions comprising water-insoluble high molecular weight oily compound

1998
- 1998-06-04 CA CA002304275A patent/CA2304275C/fr not_active Expired - Fee Related
- 1998-06-04 TR TR2000/01027T patent/TR200001027T2/xx unknown
- 1998-06-04 CN CN98811244A patent/CN1279600A/zh active Pending
- 1998-06-04 BR BR9812347-5A patent/BR9812347A/pt not_active IP Right Cessation
- 1998-06-04 WO PCT/US1998/011781 patent/WO1999013838A1/fr not_active Application Discontinuation
- 1998-06-04 KR KR1020007002882A patent/KR20010024125A/ko active IP Right Grant
- 1998-06-04 EP EP98926401A patent/EP1014919A1/fr not_active Withdrawn
2000
- 2000-03-15 NO NO20001352A patent/NO20001352L/no not_active Application Discontinuation

Also Published As

Publication number	Publication date
CN1279600A (zh)	2001-01-10
KR20010024125A (ko)	2001-03-26
EP1014919A1 (fr)	2000-07-05
WO1999013838A1 (fr)	1999-03-25
TR200001027T2 (tr)	2000-08-21
NO20001352L (no)	2000-05-18
BR9812347A (pt)	2000-09-19
CA2304275A1 (fr)	1999-03-25
NO20001352D0 (no)	2000-03-15

Publication	Publication Date	Title
CA2389714C (fr)	2007-05-29	Composition apres-shampooing antipelliculaire
US6468515B1 (en)	2002-10-22	Hair conditioning composition comprising high molecular weight ester oil
AU7824798A (en)	1999-04-05	Hair conditioning composition comprising high molecular weight ester oil
EP1328240A1 (fr)	2003-07-23	Compositions de tonifiant capillaire a base de particules
WO1999062492A1 (fr)	1999-12-09	Compositions de tonifiants capillaires
WO1999062467A1 (fr)	1999-12-09	Composition d'apres-shampoing contenant une huile de poly(alpha-olefine)
US20030215415A1 (en)	2003-11-20	Hair conditioning compositions comprising particles
CA2304275C (fr)	2002-10-08	Produit capillaire a base d'esters huiles a haute densite moleculaire
CA2388587A1 (fr)	2001-05-17	Composition apres-shampooing contenant de la cellulose cationique rendue hydrophobe
AU1410097A (en)	1998-06-29	Hair conditioning compositions comprising water-insoluble high molecular weight oily compound
AU6056100A (en)	2001-01-22	Hair conditioning composition comprising cationic silicone emulsion
WO1999062466A1 (fr)	1999-12-09	Composition de conditionnement pour cheveux contenant une huile d'ester de citrate
WO1999062468A1 (fr)	1999-12-09	Composition d'apres-shampooing comprenant une huile primaire et une huile secondaire
WO2000006094A1 (fr)	2000-02-10	Composition pour les cheveux comprenant des antioxydants
WO2000064412A1 (fr)	2000-11-02	Compositions d'apres-shampoing
EP1032365A1 (fr)	2000-09-06	Compositions pour traitement capillaire comprenant des tensioactifs cationiques hydrophiliquement substitues et des composes a point de fusion eleve
MXPA00002664A (en)	2001-05-17	Hair conditioning composition comprising high molecular weight ester oil
MXPA00011992A (en)	2001-07-31	HAIR CONDITIONING COMPOSITION COMPRISING POLY&agr;-OLEFIN OIL
MXPA00011991A (es)	2001-07-31	Composición acondicionadora del cabello que comprende aceite primario y aceite secundario
MXPA00004589A (en)	2001-05-07	Hair conditioning compositions comprising hydrophilically substituted cationic surfactants and high melting point compounds

Legal Events

Date	Code	Title	Description
2000-03-16	EEER	Examination request
2005-06-06	MKLA	Lapsed