JP4913033B2 - ヘアトリートメント組成物 - Google Patents
ヘアトリートメント組成物 Download PDFInfo
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- JP4913033B2 JP4913033B2 JP2007502220A JP2007502220A JP4913033B2 JP 4913033 B2 JP4913033 B2 JP 4913033B2 JP 2007502220 A JP2007502220 A JP 2007502220A JP 2007502220 A JP2007502220 A JP 2007502220A JP 4913033 B2 JP4913033 B2 JP 4913033B2
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- 239000000203 mixture Substances 0.000 title claims abstract description 113
- 238000009472 formulation Methods 0.000 claims abstract description 50
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 23
- 239000003093 cationic surfactant Substances 0.000 claims abstract description 15
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 10
- 125000003118 aryl group Chemical group 0.000 claims abstract description 10
- UNYNVICDCJHOPO-UHFFFAOYSA-N quabalactone III Natural products CC1OC(=O)C(O)=C1C UNYNVICDCJHOPO-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims abstract description 5
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims abstract description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims abstract description 5
- 125000002877 alkyl aryl group Chemical group 0.000 claims abstract description 5
- 150000001450 anions Chemical class 0.000 claims abstract description 5
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 5
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 5
- VXAPDXVBDZRZKP-UHFFFAOYSA-N nitric acid phosphoric acid Chemical compound O[N+]([O-])=O.OP(O)(O)=O VXAPDXVBDZRZKP-UHFFFAOYSA-N 0.000 claims abstract description 5
- -1 lactate ion Chemical group 0.000 claims description 37
- 238000000034 method Methods 0.000 claims description 16
- PHOQVHQSTUBQQK-SQOUGZDYSA-N D-glucono-1,5-lactone Chemical compound OC[C@H]1OC(=O)[C@H](O)[C@@H](O)[C@@H]1O PHOQVHQSTUBQQK-SQOUGZDYSA-N 0.000 claims description 6
- 235000012209 glucono delta-lactone Nutrition 0.000 claims description 6
- 229960003681 gluconolactone Drugs 0.000 claims description 6
- 239000001993 wax Substances 0.000 claims description 6
- 235000013871 bee wax Nutrition 0.000 claims description 5
- 239000012166 beeswax Substances 0.000 claims description 5
- 150000008051 alkyl sulfates Chemical class 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 abstract description 3
- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 abstract 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 abstract 1
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 1
- 229920001296 polysiloxane Polymers 0.000 description 30
- 239000003921 oil Substances 0.000 description 22
- 235000019198 oils Nutrition 0.000 description 22
- 230000003750 conditioning effect Effects 0.000 description 19
- 229920006395 saturated elastomer Polymers 0.000 description 13
- 229930195733 hydrocarbon Natural products 0.000 description 11
- 150000002430 hydrocarbons Chemical class 0.000 description 11
- 235000014113 dietary fatty acids Nutrition 0.000 description 10
- 239000000194 fatty acid Substances 0.000 description 10
- 229930195729 fatty acid Natural products 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 9
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 239000004215 Carbon black (E152) Substances 0.000 description 7
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 7
- 150000002191 fatty alcohols Chemical class 0.000 description 7
- 125000002091 cationic group Chemical group 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 230000002209 hydrophobic effect Effects 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
- 230000008961 swelling Effects 0.000 description 5
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 239000004205 dimethyl polysiloxane Substances 0.000 description 4
- 150000002194 fatty esters Chemical class 0.000 description 4
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 235000010446 mineral oil Nutrition 0.000 description 4
- 239000002480 mineral oil Substances 0.000 description 4
- 229920001451 polypropylene glycol Polymers 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 3
- 239000003240 coconut oil Substances 0.000 description 3
- 235000019864 coconut oil Nutrition 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 229940008099 dimethicone Drugs 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 125000001453 quaternary ammonium group Chemical group 0.000 description 3
- 239000002453 shampoo Substances 0.000 description 3
- 229920005573 silicon-containing polymer Polymers 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical class CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- OSCJHTSDLYVCQC-UHFFFAOYSA-N 2-ethylhexyl 4-[[4-[4-(tert-butylcarbamoyl)anilino]-6-[4-(2-ethylhexoxycarbonyl)anilino]-1,3,5-triazin-2-yl]amino]benzoate Chemical compound C1=CC(C(=O)OCC(CC)CCCC)=CC=C1NC1=NC(NC=2C=CC(=CC=2)C(=O)NC(C)(C)C)=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=N1 OSCJHTSDLYVCQC-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical group N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- VZWGRQBCURJOMT-UHFFFAOYSA-N Dodecyl acetate Chemical compound CCCCCCCCCCCCOC(C)=O VZWGRQBCURJOMT-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 235000019486 Sunflower oil Nutrition 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 229960000541 cetyl alcohol Drugs 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 150000004820 halides Chemical group 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- CBFCDTFDPHXCNY-UHFFFAOYSA-N icosane Chemical compound CCCCCCCCCCCCCCCCCCCC CBFCDTFDPHXCNY-UHFFFAOYSA-N 0.000 description 2
- 229940093629 isopropyl isostearate Drugs 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 2
- SSZBUIDZHHWXNJ-UHFFFAOYSA-N palmityl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCC SSZBUIDZHHWXNJ-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 229920001083 polybutene Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- NEOZOXKVMDBOSG-UHFFFAOYSA-N propan-2-yl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OC(C)C NEOZOXKVMDBOSG-UHFFFAOYSA-N 0.000 description 2
- 210000004761 scalp Anatomy 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 239000002600 sunflower oil Substances 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- 150000003626 triacylglycerols Chemical class 0.000 description 2
- OQQOAWVKVDAJOI-UHFFFAOYSA-N (2-dodecanoyloxy-3-hydroxypropyl) dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCCCCC OQQOAWVKVDAJOI-UHFFFAOYSA-N 0.000 description 1
- HKBNTEUXXLLXHI-UHFFFAOYSA-N 1,1'-biphenyl;trimethylazanium;chloride Chemical compound [Cl-].C[NH+](C)C.C1=CC=CC=C1C1=CC=CC=C1 HKBNTEUXXLLXHI-UHFFFAOYSA-N 0.000 description 1
- JQJSFAJISYZPER-UHFFFAOYSA-N 1-(4-chlorophenyl)-3-(2,3-dihydro-1h-inden-5-ylsulfonyl)urea Chemical compound C1=CC(Cl)=CC=C1NC(=O)NS(=O)(=O)C1=CC=C(CCC2)C2=C1 JQJSFAJISYZPER-UHFFFAOYSA-N 0.000 description 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- FDCJDKXCCYFOCV-UHFFFAOYSA-N 1-hexadecoxyhexadecane Chemical compound CCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCC FDCJDKXCCYFOCV-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- HBXWUCXDUUJDRB-UHFFFAOYSA-N 1-octadecoxyoctadecane Chemical compound CCCCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCCCC HBXWUCXDUUJDRB-UHFFFAOYSA-N 0.000 description 1
- XFOQWQKDSMIPHT-UHFFFAOYSA-N 2,3-dichloro-6-(trifluoromethyl)pyridine Chemical compound FC(F)(F)C1=CC=C(Cl)C(Cl)=N1 XFOQWQKDSMIPHT-UHFFFAOYSA-N 0.000 description 1
- RRLKOZCPQXMIIJ-UHFFFAOYSA-N 2,4,4-trimethylnonane Chemical compound CCCCCC(C)(C)CC(C)C RRLKOZCPQXMIIJ-UHFFFAOYSA-N 0.000 description 1
- RWBHOLZDSPWSPK-UHFFFAOYSA-N 2,4,4-trimethylundecane Chemical compound CCCCCCCC(C)(C)CC(C)C RWBHOLZDSPWSPK-UHFFFAOYSA-N 0.000 description 1
- FSAMVJAGJWGWTQ-UHFFFAOYSA-N 2-hexadecoxyethanol Chemical compound CCCCCCCCCCCCCCCCOCCO FSAMVJAGJWGWTQ-UHFFFAOYSA-N 0.000 description 1
- MUHFRORXWCGZGE-KTKRTIGZSA-N 2-hydroxyethyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCO MUHFRORXWCGZGE-KTKRTIGZSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- XTQUSEDRZLDHRC-UHFFFAOYSA-N 3-octadecanoyloxybutyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCC(C)OC(=O)CCCCCCCCCCCCCCCCC XTQUSEDRZLDHRC-UHFFFAOYSA-N 0.000 description 1
- NZXZINXFUSKTPH-UHFFFAOYSA-N 4-[4-(4-butylcyclohexyl)cyclohexyl]-1,2-difluorobenzene Chemical compound C1CC(CCCC)CCC1C1CCC(C=2C=C(F)C(F)=CC=2)CC1 NZXZINXFUSKTPH-UHFFFAOYSA-N 0.000 description 1
- HBTAOSGHCXUEKI-UHFFFAOYSA-N 4-chloro-n,n-dimethyl-3-nitrobenzenesulfonamide Chemical compound CN(C)S(=O)(=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 HBTAOSGHCXUEKI-UHFFFAOYSA-N 0.000 description 1
- IBYCEACZVUOBIV-UHFFFAOYSA-N 4-methylpentyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCC(C)C IBYCEACZVUOBIV-UHFFFAOYSA-N 0.000 description 1
- AUGIYYGVQDZOLU-UHFFFAOYSA-N 4-methylpentyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCC(C)C AUGIYYGVQDZOLU-UHFFFAOYSA-N 0.000 description 1
- ODMZDMMTKHXXKA-QXMHVHEDSA-N 8-methylnonyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCCCCCCC(C)C ODMZDMMTKHXXKA-QXMHVHEDSA-N 0.000 description 1
- 235000019489 Almond oil Nutrition 0.000 description 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 208000001840 Dandruff Diseases 0.000 description 1
- 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 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- CMBYOWLFQAFZCP-UHFFFAOYSA-N Hexyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCCCC CMBYOWLFQAFZCP-UHFFFAOYSA-N 0.000 description 1
- 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 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 241000446313 Lamella Species 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- CMCJFUXWBBHIIL-UHFFFAOYSA-N Propylene glycol stearate Chemical class CC(O)CO.CCCCCCCCCCCCCCCCCC(O)=O CMCJFUXWBBHIIL-UHFFFAOYSA-N 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- BAECOWNUKCLBPZ-HIUWNOOHSA-N Triolein Natural products O([C@H](OCC(=O)CCCCCCC/C=C\CCCCCCCC)COC(=O)CCCCCCC/C=C\CCCCCCCC)C(=O)CCCCCCC/C=C\CCCCCCCC BAECOWNUKCLBPZ-HIUWNOOHSA-N 0.000 description 1
- PHYFQTYBJUILEZ-UHFFFAOYSA-N Trioleoylglycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCCCCCCCC)COC(=O)CCCCCCCC=CCCCCCCCC PHYFQTYBJUILEZ-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 229910001508 alkali metal halide Inorganic materials 0.000 description 1
- 150000008045 alkali metal halides Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000008168 almond oil Substances 0.000 description 1
- 150000001408 amides Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229920013822 aminosilicone Polymers 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000008163 avocado oil Substances 0.000 description 1
- 235000021302 avocado oil Nutrition 0.000 description 1
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical compound CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 description 1
- IUGNTDSUZLPSOK-UHFFFAOYSA-N bis(4-methylpentyl) hexanedioate Chemical compound CC(C)CCCOC(=O)CCCCC(=O)OCCCC(C)C IUGNTDSUZLPSOK-UHFFFAOYSA-N 0.000 description 1
- 229940006460 bromide ion Drugs 0.000 description 1
- NZIKRHKSEITLPS-UHFFFAOYSA-N butane-1,3-diol;octadecanoic acid Chemical compound CC(O)CCO.CCCCCCCCCCCCCCCCCC(O)=O NZIKRHKSEITLPS-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 125000000837 carbohydrate group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 229940081733 cetearyl alcohol Drugs 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229940110456 cocoa butter Drugs 0.000 description 1
- 235000019868 cocoa butter Nutrition 0.000 description 1
- 235000012716 cod liver oil Nutrition 0.000 description 1
- 239000003026 cod liver oil Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000012612 commercial material Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920013750 conditioning polymer Polymers 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- KBODESQIOVVMAI-UHFFFAOYSA-N decyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCC KBODESQIOVVMAI-UHFFFAOYSA-N 0.000 description 1
- SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 229940031578 diisopropyl adipate Drugs 0.000 description 1
- 229940031569 diisopropyl sebacate Drugs 0.000 description 1
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
- XFKBBSZEQRFVSL-UHFFFAOYSA-N dipropan-2-yl decanedioate Chemical compound CC(C)OC(=O)CCCCCCCCC(=O)OC(C)C XFKBBSZEQRFVSL-UHFFFAOYSA-N 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- SNRUBQQJIBEYMU-NJFSPNSNSA-N dodecane Chemical class CCCCCCCCCCC[14CH3] SNRUBQQJIBEYMU-NJFSPNSNSA-N 0.000 description 1
- QQQMUBLXDAFBRH-UHFFFAOYSA-N dodecyl 2-hydroxypropanoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)O QQQMUBLXDAFBRH-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000000182 glucono-delta-lactone Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229940074049 glyceryl dilaurate Drugs 0.000 description 1
- DCAYPVUWAIABOU-NJFSPNSNSA-N hexadecane Chemical class CCCCCCCCCCCCCCC[14CH3] DCAYPVUWAIABOU-NJFSPNSNSA-N 0.000 description 1
- RSRQBSGZMPVCOI-UHFFFAOYSA-N hexadecyl propanoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)CC RSRQBSGZMPVCOI-UHFFFAOYSA-N 0.000 description 1
- 229940100463 hexyl laurate Drugs 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- WVJVHUWVQNLPCR-UHFFFAOYSA-N octadecanoyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(=O)CCCCCCCCCCCCCCCCC WVJVHUWVQNLPCR-UHFFFAOYSA-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
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- YCOZIPAWZNQLMR-UHFFFAOYSA-N pentadecane Chemical class CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 150000003335 secondary amines Chemical group 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 150000003512 tertiary amines Chemical group 0.000 description 1
- BGHCVCJVXZWKCC-NJFSPNSNSA-N tetradecane Chemical class CCCCCCCCCCCCC[14CH3] BGHCVCJVXZWKCC-NJFSPNSNSA-N 0.000 description 1
- BORJONZPSTVSFP-UHFFFAOYSA-N tetradecyl 2-hydroxypropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)C(C)O BORJONZPSTVSFP-UHFFFAOYSA-N 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- IIYFAKIEWZDVMP-NJFSPNSNSA-N tridecane Chemical class CCCCCCCCCCCC[14CH3] IIYFAKIEWZDVMP-NJFSPNSNSA-N 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- UKBHVNMEMHTWQO-UHFFFAOYSA-N trioctadecyl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CC(O)(C(=O)OCCCCCCCCCCCCCCCCCC)CC(=O)OCCCCCCCCCCCCCCCCCC UKBHVNMEMHTWQO-UHFFFAOYSA-N 0.000 description 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
- 229940117972 triolein Drugs 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 230000000007 visual effect Effects 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
- A61K8/89—Polysiloxanes
- A61K8/895—Polysiloxanes containing silicon bound to unsaturated aliphatic groups, e.g. vinyl dimethicone
-
- 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
- A61K8/60—Sugars; Derivatives thereof
-
- 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
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
- A61K8/927—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of insects, e.g. shellac
-
- 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
- A61Q5/04—Preparations for permanent waving or straightening the hair
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Insects & Arthropods (AREA)
- Zoology (AREA)
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Description
i)糖ラクトンを、処方物全体の0.1から7.9重量%と;
ii)式1:
[N(R1)(R2)(R3)(R4)]+(X)− 式1
の陽イオン界面活性剤(式中、R1、R2、R3及びR4は、(a)1個から22個の炭素原子の脂肪族基又は(b)22個以下の炭素原子を有する、芳香族、アルコキシ、ポリオキシアルキレン、アルキルアミド、ヒドロキシアルキル、アリール又はアルキルアリール基から独立に選択され;Xは、ハロゲン、酢酸イオン、クエン酸イオン、乳酸イオン、グリコール酸イオン、硝酸リン酸イオン、硫酸イオン及びアルキル硫酸イオンから選択される、塩形成陰イオンである。)と、を含有するヘアトリートメント組成物に関する。
本発明による組成物は、化粧品として許容可能であり毛髪への局所適用に適切な、1又は複数の陽イオン性コンディショニング界面活性剤を含有する。
[N(R1)(R2)(R3)(R4)]+(X)− 式1
に対応するものである(式中、R1、R2、R3及びR4は、(a)1個から22個の炭素原子の脂肪族基又は(b)22個以下の炭素原子を有する、芳香族、アルコキシ、ポリオキシアルキレン、アルキルアミド、ヒドロキシアルキル、アリール又はアルキルアリール基から独立に選択され;Xは、ハロゲン(例えば塩化イオン、臭化イオン)、酢酸イオン、クエン酸イオン、乳酸イオン、グリコール酸イオン、硝酸リン酸イオン、硫酸イオン及びアルキル硫酸イオンから選択されるものなどの、塩形成陰イオンである。)
本発明の組成物は、糖ラクトン、好ましくはグルコノラクトン、特に、グルコノ−δ−ラクトンを含有する。
本発明の組成物は、好ましくは、ワックスを含有する。蜜ロウは、知覚的な面で欠点なく、毛髪をさらに直毛化するので、本組成物において好ましいワックスである。
本発明のコンディショナー組成物は、好ましくは、少なくとも1つの脂肪物質を含有する。本コンディショニング組成物中で脂肪物質と陽イオン界面活性剤とを組み合わせて使用することにより、構造化ラメラ又は液晶相が形成され、そこに陽イオン界面活性剤が分散される、と考えられる。
本組成物は、ハロゲン化アルカリ金属又はそれらの混合物を含有し得る。
本発明による組成物の好ましい成分は、疎水性コンディショニング油である。本発明による組成物中で離散液滴として好ましい形態でこのような油が存在するために、これは水不溶性でなければならない。水不溶性とは、水中での溶解度が、25℃にて0.01重量%以下であることを意味する。
本発明による組成物における使用に対して好ましい疎水性コンディショニング油は、シリコーンである。
本発明による組成物はまた、その他の化粧品として適切な成分を、好ましくは2重量%以下の濃度で組み込み得る。適切な成分には、粘度調整剤、保存料、着色剤、ポリオール(グリセリン及びポリプロピレングリコールなど)、キレート剤(EDTAなど)、抗酸化剤、香料、抗菌剤、フケ防止剤、陽イオン性コンディショニングポリマー、スタイリング成分、サンスクリーン、タンパク質及びタンパク質加水分解物が含まれる。
シャンプーベースで入れ毛を2回洗浄し、50%RH及び23℃で一晩そのまま乾燥させた。写真を撮影した。1.0g シャンプーベースでその入れ毛を2回洗浄し、目の粗い櫛で梳かした。次に、実施例の表で詳述するように、その入れ毛を2.0g コンディショナー処方物で2分間トリートメントした。そのコンディショナーを洗い流し、目の粗い櫛でその入れ毛を梳かし、50%RH及び23℃で一晩、乾燥させた。その入れ毛の写真を撮影した。パネリストが、トリートメント前後に撮影した入れ毛の写真を評価し、標準的なコンディショナー組成物でトリートメントした入れ毛と比較した、直毛化効果を観察した。
家庭での使用による単項試験において、パネリストによる処方物5、6及び7の評価を行った。各コンディショナー処方物を評価するパネリストの人数は、50名であった。5個の代表的処方物及び対照処方物を試験した。消費者総数=300である。試験期間は2週間で、消費者は、この代表的処方物を最低6回の洗浄で使用した。コンディショナー処方物の塗布直前に、標準的シャンプー処方物を使用のために供給した。
Claims (11)
- i)糖ラクトンを、処方物全体の0.1から7.9重量%と;
ii)式1:
[N(R1)(R2)(R3)(R4)]+(X)− 式1
の陽イオン界面活性剤(式中、R1、R2、R3及びR4は、(a)1個から22個の炭素原子の脂肪族基又は(b)22個以下の炭素原子を有する、芳香族、アルコキシ、ポリオキシアルキレン、アルキルアミド、ヒドロキシアルキル、アリール又はアルキルアリール基から独立に選択され;Xは、ハロゲン、酢酸イオン、クエン酸イオン、乳酸イオン、グリコール酸イオン、硝酸リン酸イオン、硫酸イオン及びアルキル硫酸イオンから選択される、塩形成陰イオンである。)と、を含有する、
組成物を毛髪に塗布する段階を含む、毛髪を直毛化する方法。 - 前記組成物内の糖ラクトンがグルコノラクトンである、請求項1に記載の方法。
- 糖ラクトン濃度が、前記組成物全体の0.5重量%を超える、請求項1又は2に記載の方法。
- 糖ラクトン濃度が、前記組成物全体の2重量%から6重量%である、請求項3に記載の方法。
- 陽イオン界面活性剤濃度が、前記組成物全体の0.1重量%から15重量%である、請求項1〜4のいずれか一項に記載の方法。
- 前記組成物がワックスをさらに含有する、請求項1〜5のいずれか一項に記載の方法。
- 前記ワックスが、蜜ロウである、請求項6に記載の方法。
- 前記組成物が洗い流される、請求項1〜7のいずれか一項に記載の方法。
- 機械的介入なく毛髪が直毛化される、請求項1〜8のいずれか一項に記載の毛髪を直毛化する方法。
- 前記組成物が毛髪に塗布され、次いで、塗布後30分以内に該毛髪から洗い流される、請求項9に記載の毛髪を直毛化する方法。
- i)糖ラクトンを、処方物全体の0.1から7.9重量%と;
ii)式1:
[N(R 1 )(R 2 )(R 3 )(R 4 )] + (X) − 式1
の陽イオン界面活性剤(式中、R 1 、R 2 、R 3 及びR 4 は、(a)1個から22個の炭素原子の脂肪族基又は(b)22個以下の炭素原子を有する、芳香族、アルコキシ、ポリオキシアルキレン、アルキルアミド、ヒドロキシアルキル、アリール又はアルキルアリール基から独立に選択され;Xは、ハロゲン、酢酸イオン、クエン酸イオン、乳酸イオン、グリコール酸イオン、硝酸リン酸イオン、硫酸イオン及びアルキル硫酸イオンから選択される、塩形成陰イオンである。)と、を含有する、
組成物の、毛髪を直毛化するための使用。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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EP04251324 | 2004-03-08 | ||
EP04251324.2 | 2004-03-08 | ||
PCT/EP2005/001822 WO2005084623A1 (en) | 2004-03-08 | 2005-02-18 | Hair treatment composition |
Publications (2)
Publication Number | Publication Date |
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JP2007527878A JP2007527878A (ja) | 2007-10-04 |
JP4913033B2 true JP4913033B2 (ja) | 2012-04-11 |
Family
ID=34917211
Family Applications (1)
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JP2007502220A Expired - Fee Related JP4913033B2 (ja) | 2004-03-08 | 2005-02-18 | ヘアトリートメント組成物 |
Country Status (8)
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US (1) | US8192730B2 (ja) |
EP (1) | EP1722750B1 (ja) |
JP (1) | JP4913033B2 (ja) |
CN (2) | CN100528128C (ja) |
AT (1) | ATE407655T1 (ja) |
BR (1) | BRPI0507821A (ja) |
DE (1) | DE602005009667D1 (ja) |
WO (1) | WO2005084623A1 (ja) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BRPI0508137B1 (pt) * | 2004-03-08 | 2017-10-24 | Unilever N.V | Aquosa cleaning composition for hair dispersion treatment, hair dispersion method and use of a composition |
US20060083704A1 (en) * | 2004-10-19 | 2006-04-20 | Torgerson Peter M | Hair conditioning composition comprising high internal phase viscosity silicone copolymer emulsions |
EA201071293A1 (ru) * | 2008-05-12 | 2011-04-29 | Унилевер Н.В. | Композиция для укладки волос |
FR2944960B1 (fr) * | 2009-04-30 | 2012-09-14 | Oreal | Utilisation d'un liquide ionique pour la mise en forme permanente des fibres keratiniques |
ITMC20100030A1 (it) * | 2010-02-24 | 2011-08-25 | Alderan S A S Di Alderano Mannozzi & C | Uso di glucidi per rendere liscio il capello riccio, crespo od ondulato. |
EA026458B1 (ru) | 2012-05-21 | 2017-04-28 | Юнилевер Н.В. | Способ обработки волос |
BR112014028727B1 (pt) | 2012-05-21 | 2020-03-10 | Unilever N.V. | Método de alisamento do cabelo |
JP6220387B2 (ja) | 2012-05-21 | 2017-10-25 | ユニリーバー・ナームローゼ・ベンノートシヤープ | 毛髪を処理する方法 |
FR3001385B1 (fr) * | 2013-01-31 | 2015-10-30 | Oreal | Composition comprenant un diacide carboxylique et une huile et procede de lissage des cheveux |
WO2015074846A1 (en) * | 2013-11-21 | 2015-05-28 | Unilever Plc | Method of shaping hair |
BR112016009672B1 (pt) | 2013-11-21 | 2020-07-21 | Unilever Nv. | método para modelar os cabelos |
US10588839B2 (en) | 2013-11-21 | 2020-03-17 | Conopco, Inc. | Method of shaping hair |
EA033701B1 (ru) * | 2015-07-21 | 2019-11-18 | Unilever Nv | Композиция для придания формы волосам |
EP3325102B1 (en) * | 2015-07-21 | 2019-01-23 | Unilever PLC | Hair shaping composition |
FR3083104B1 (fr) * | 2018-06-29 | 2020-06-12 | L'oreal | Procede de mise en forme des cheveux comprenant une etape d’application d’une composition comprenant une lactone, une etape de mise en forme et un long temps de pause |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB915816A (en) * | 1959-07-14 | 1963-01-16 | Colgate Palmolive Co | Acidic cosmetic preparations and processes for their manufacture |
JPH06298629A (ja) * | 1993-04-19 | 1994-10-25 | Kao Corp | 毛髪変形剤組成物 |
JPH1171242A (ja) * | 1997-08-28 | 1999-03-16 | Lion Corp | 毛髪処理剤 |
JP2000191455A (ja) * | 1998-12-25 | 2000-07-11 | Lion Corp | 毛髪化粧料 |
JP2002003342A (ja) * | 2000-06-26 | 2002-01-09 | Kanebo Ltd | 毛髪化粧料 |
JP2003089620A (ja) * | 2001-09-19 | 2003-03-28 | Lion Corp | 毛髪化粧料 |
JP2003300811A (ja) * | 2002-04-05 | 2003-10-21 | Lion Corp | ロスマリン酸含有組成物 |
JP2004026770A (ja) * | 2002-06-28 | 2004-01-29 | Milbon Co Ltd | 縮毛矯正用第1剤およびそれを用いた縮毛の矯正処理方法 |
JP2007509182A (ja) * | 2003-10-27 | 2007-04-12 | ユニリーバー・ナームローゼ・ベンノートシヤープ | ヘアケア組成物 |
Family Cites Families (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL6410355A (ja) | 1963-09-06 | 1965-03-08 | ||
US3470887A (en) | 1965-10-21 | 1969-10-07 | Natcon Chem Co Inc | Method for straightening hair and composition of matter for use therewith |
US3822238A (en) * | 1972-08-02 | 1974-07-02 | Princeton Polymer Lab | Hydrophilic polyurethane polymers |
US4156066A (en) * | 1977-06-23 | 1979-05-22 | Tyndale Plains - Hunter Ltd. | Polyurethane polymers characterized by lactone groups and hydroxyl groups in the polymer backbone |
US4255550A (en) * | 1978-12-22 | 1981-03-10 | Tyndale Plains - Hunter Ltd. | Polyurethane polymers characterized by carboxylate groups and hydroxyl groups in the polymer backbone |
US4460571A (en) * | 1982-03-29 | 1984-07-17 | Gomez Dominador S | Cosmetic composition |
US4786493A (en) * | 1985-11-22 | 1988-11-22 | Estee Lauder Inc. | Hair protection composition |
US4911919A (en) * | 1986-06-17 | 1990-03-27 | Colgate-Palmolive Company | Hair straightening conditioner |
US4743673A (en) * | 1986-12-19 | 1988-05-10 | Tyndale Plains-Hunter, Ltd. | Hydrophilic carboxy polyurethanes |
US5942250A (en) * | 1986-12-23 | 1999-08-24 | Tristrata Technology, Inc. | Compositions and methods for enhancing the topical effects of sunscreen agents |
US5547988B1 (en) * | 1986-12-23 | 1997-07-15 | Tristrata Inc | Alleviating signs of dermatological aging with glycolic acid lactic acid or citric acid |
US6384079B1 (en) | 1986-12-23 | 2002-05-07 | Tristrata Technology, Incorporated | Compositions comprising 2-hydroxycarboxylic acids and related compounds, and methods for alleviating signs of dermatological aging |
US5077042A (en) | 1988-03-25 | 1991-12-31 | Johnson Products Co., Inc. | Conditioning hair relaxer system with conditioning activator |
US5000955A (en) * | 1988-07-29 | 1991-03-19 | Tyndale Plains-Hunter Ltd. | Thermally reversible polyurethane hydrogels and cosmetic, biological and medical uses |
US5077040A (en) | 1990-04-30 | 1991-12-31 | Helene Curtis, Inc. | Hair-treating microemulsion composition and method of preparing and using the same |
GB9116871D0 (en) | 1991-08-05 | 1991-09-18 | Unilever Plc | Hair care composition |
US5507970A (en) * | 1992-05-29 | 1996-04-16 | Lion Corporation | Detergent composition |
EP0619111B2 (en) | 1993-04-06 | 2005-09-14 | National Starch and Chemical Investment Holding Corporation | Use of polyurethanes with carboxylate functionality for hair fixative applications |
EP0664692B1 (de) * | 1993-06-23 | 2000-10-25 | Wella Aktiengesellschaft | Wässriges mittel zur festigung von haaren in form eines hochviskosen, versprühbaren gels |
EP0640643B1 (en) * | 1993-08-10 | 2000-04-26 | Kao Corporation | Organopolysiloxanes and a method of setting hair using the same |
US5641477A (en) * | 1994-11-28 | 1997-06-24 | Avlon Industries, Inc. | Reduction of hair damage during lanthionization with hair relaxers containing deswelling agents |
US5641480A (en) * | 1994-12-08 | 1997-06-24 | Lever Brothers Company, Division Of Conopco, Inc. | Hair care compositions comprising heteroatom containing alkyl aldonamide compounds |
DE19902246C5 (de) | 1999-01-21 | 2004-11-04 | Wella Ag | Verfahren und Mittel zur dauerhaften Haarverformung mit zeitabhängiger Reduzierung der Wellwirksamkeit |
JP2001055571A (ja) | 1999-08-17 | 2001-02-27 | Morinaga Milk Ind Co Ltd | 抗酸化組成物 |
JP2001233746A (ja) | 2000-02-23 | 2001-08-28 | Miyoshi Oil & Fat Co Ltd | リンス基剤 |
DE10059749A1 (de) | 2000-12-01 | 2002-06-20 | Henkel Kgaa | Fixierung von Wirkstoffen an fasrigen Materialien |
JP2002356408A (ja) * | 2001-05-30 | 2002-12-13 | Milbon Co Ltd | ヘアトリートメントおよびそれを用いた毛髪のセット方法 |
US6782895B2 (en) * | 2001-08-20 | 2004-08-31 | L'oreal, S.A. | Compositions comprising at least one hydroxide compound and at least one complexing agent, and methods for using the same |
FR2830759B1 (fr) | 2001-10-15 | 2003-12-12 | Oreal | Composition sous forme d'emulsion huile-dans-eau contenant un copolymere silicone et ses utilisations notamment cosmetiques |
EP1590009B1 (en) * | 2002-10-22 | 2012-06-06 | Allegiance Corporation | Coating composition for skin-contacting surface of elastomeric articles and articles containing the same |
MXPA05004131A (es) | 2002-10-22 | 2005-06-22 | Oreal | Composiciones estilizantes duraderas activadas por calor consistentes en compuestos de tipo sacarido y agentes formadores de pelicula. |
BRPI0508137B1 (pt) * | 2004-03-08 | 2017-10-24 | Unilever N.V | Aquosa cleaning composition for hair dispersion treatment, hair dispersion method and use of a composition |
US7374750B2 (en) * | 2004-05-14 | 2008-05-20 | Jennifer Albano | Probiotic containing anhydrous hair care composition |
WO2006061678A1 (en) | 2004-12-06 | 2006-06-15 | Sederma Sas | Cosmetic or dermatological compositiions of saccharose substitutes |
JP2006232820A (ja) | 2005-01-26 | 2006-09-07 | Hayashibara Biochem Lab Inc | 毛髪セット力増強剤及び毛髪セット力増強方法並びに毛髪セット用組成物 |
JP2006282566A (ja) | 2005-03-31 | 2006-10-19 | Kose Corp | 整髪料 |
HUP0500582A1 (hu) | 2005-06-13 | 2007-08-28 | Csaba Jozsef Dr Jaszberenyi | Szinergetikus élettani hatású élelmiszerek, élelmiszer-adalékok és táplálék-kiegészítõk vagy takarmányadalékok |
FR2899464B1 (fr) | 2006-04-07 | 2008-06-06 | Oreal | Compose c-glycoside et utilisation comme agent activateur et regulateur de l'immunite cutanee |
EP1880710A1 (en) | 2006-07-21 | 2008-01-23 | Wella Aktiengesellschaft | Method and composition for permanently shaping hair |
-
2005
- 2005-02-11 CN CNB2005800072969A patent/CN100528128C/zh active Active
- 2005-02-18 JP JP2007502220A patent/JP4913033B2/ja not_active Expired - Fee Related
- 2005-02-18 AT AT05715446T patent/ATE407655T1/de not_active IP Right Cessation
- 2005-02-18 DE DE602005009667T patent/DE602005009667D1/de not_active Expired - Fee Related
- 2005-02-18 WO PCT/EP2005/001822 patent/WO2005084623A1/en active IP Right Grant
- 2005-02-18 EP EP05715446A patent/EP1722750B1/en not_active Not-in-force
- 2005-02-18 BR BRPI0507821-0A patent/BRPI0507821A/pt not_active Application Discontinuation
- 2005-02-18 US US10/592,221 patent/US8192730B2/en not_active Expired - Fee Related
- 2005-02-18 CN CN2005800074080A patent/CN1929810B/zh not_active Expired - Fee Related
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB915816A (en) * | 1959-07-14 | 1963-01-16 | Colgate Palmolive Co | Acidic cosmetic preparations and processes for their manufacture |
JPH06298629A (ja) * | 1993-04-19 | 1994-10-25 | Kao Corp | 毛髪変形剤組成物 |
JPH1171242A (ja) * | 1997-08-28 | 1999-03-16 | Lion Corp | 毛髪処理剤 |
JP2000191455A (ja) * | 1998-12-25 | 2000-07-11 | Lion Corp | 毛髪化粧料 |
JP2002003342A (ja) * | 2000-06-26 | 2002-01-09 | Kanebo Ltd | 毛髪化粧料 |
JP2003089620A (ja) * | 2001-09-19 | 2003-03-28 | Lion Corp | 毛髪化粧料 |
JP2003300811A (ja) * | 2002-04-05 | 2003-10-21 | Lion Corp | ロスマリン酸含有組成物 |
JP2004026770A (ja) * | 2002-06-28 | 2004-01-29 | Milbon Co Ltd | 縮毛矯正用第1剤およびそれを用いた縮毛の矯正処理方法 |
JP2007509182A (ja) * | 2003-10-27 | 2007-04-12 | ユニリーバー・ナームローゼ・ベンノートシヤープ | ヘアケア組成物 |
Also Published As
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---|---|
CN1929810A (zh) | 2007-03-14 |
EP1722750A1 (en) | 2006-11-22 |
BRPI0507821A (pt) | 2007-07-10 |
CN1929814A (zh) | 2007-03-14 |
ATE407655T1 (de) | 2008-09-15 |
US8192730B2 (en) | 2012-06-05 |
EP1722750B1 (en) | 2008-09-10 |
DE602005009667D1 (de) | 2008-10-23 |
CN1929810B (zh) | 2010-05-05 |
WO2005084623A1 (en) | 2005-09-15 |
CN100528128C (zh) | 2009-08-19 |
JP2007527878A (ja) | 2007-10-04 |
US20080019938A1 (en) | 2008-01-24 |
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