DE102009046196A1 - Tönungsmittel - Google Patents

Tönungsmittel Download PDF

Info

Publication number: DE102009046196A1
Authority: DE; Germany
Prior art keywords: amino; bis; acid; group; und
Prior art date: 2009-10-30
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 Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Withdrawn

Application number

DE200910046196

Other languages

German (de)

English (en)

Inventor

Diane Metten

Ina Franke

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.)

Henkel AG and Co KGaA

Original Assignee

Henkel AG and Co KGaA

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.)

2009-10-30

Filing date

2009-10-30

Publication date

2011-05-05

2009-10-30 Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA

2009-10-30 Priority to DE200910046196 priority Critical patent/DE102009046196A1/de

2010-10-07 Priority to PCT/EP2010/064969 priority patent/WO2011051087A1/fr

2011-05-05 Publication of DE102009046196A1 publication Critical patent/DE102009046196A1/de

Status Withdrawn legal-status Critical Current

Links

239000003795 chemical substances by application Substances 0.000 claims abstract description 66
239000002243 precursor Substances 0.000 claims abstract description 29
239000000835 fiber Substances 0.000 claims abstract description 28
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims abstract description 16
229920001577 copolymer Polymers 0.000 claims description 72
239000000975 dye Substances 0.000 claims description 45
210000004209 hair Anatomy 0.000 claims description 40
239000000203 mixture Substances 0.000 claims description 35
239000000982 direct dye Substances 0.000 claims description 33
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 20
229920000642 polymer Polymers 0.000 claims description 19
229920002125 Sokalan® Polymers 0.000 claims description 16
238000000034 method Methods 0.000 claims description 12
125000002091 cationic group Chemical group 0.000 claims description 11
238000011282 treatment Methods 0.000 claims description 11
NJSSICCENMLTKO-HRCBOCMUSA-N [(1r,2s,4r,5r)-3-hydroxy-4-(4-methylphenyl)sulfonyloxy-6,8-dioxabicyclo[3.2.1]octan-2-yl] 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)O[C@H]1C(O)[C@@H](OS(=O)(=O)C=2C=CC(C)=CC=2)[C@@H]2OC[C@H]1O2 NJSSICCENMLTKO-HRCBOCMUSA-N 0.000 claims description 10
230000008859 change Effects 0.000 claims description 10
125000000129 anionic group Chemical group 0.000 claims description 8
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 7
102000011782 Keratins Human genes 0.000 claims description 7
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HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 5
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CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 3
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 3
239000004584 polyacrylic acid Substances 0.000 claims description 3
150000001555 benzenes Chemical class 0.000 claims 1
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150000001875 compounds Chemical class 0.000 description 71
150000003839 salts Chemical class 0.000 description 49
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150000003254 radicals Chemical class 0.000 description 32
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125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 15
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XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
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 13
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 13
150000001252 acrylic acid derivatives Chemical class 0.000 description 13
238000002360 preparation method Methods 0.000 description 13
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
239000002253 acid Substances 0.000 description 12
239000001257 hydrogen Substances 0.000 description 12
239000000047 product Substances 0.000 description 12
239000000126 substance Substances 0.000 description 12
229960001631 carbomer Drugs 0.000 description 11
239000003086 colorant Substances 0.000 description 11
239000007787 solid Substances 0.000 description 11
CWLKGDAVCFYWJK-UHFFFAOYSA-N m-Aminophenol Natural products NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 10
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 9
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 9
235000014113 dietary fatty acids Nutrition 0.000 description 9
239000000194 fatty acid Substances 0.000 description 9
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239000000118 hair dye Substances 0.000 description 9
239000011734 sodium Substances 0.000 description 9
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239000000243 solution Substances 0.000 description 9
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DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 8
239000004480 active ingredient Substances 0.000 description 8
125000003118 aryl group Chemical group 0.000 description 8
229910052760 oxygen Inorganic materials 0.000 description 8
239000001301 oxygen Substances 0.000 description 8
WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 8
229940047670 sodium acrylate Drugs 0.000 description 8
159000000000 sodium salts Chemical class 0.000 description 8
239000002904 solvent Substances 0.000 description 8
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
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 7
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 7
GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 description 7
230000000694 effects Effects 0.000 description 7
235000013305 food Nutrition 0.000 description 7
235000011187 glycerol Nutrition 0.000 description 7
230000001590 oxidative effect Effects 0.000 description 7
125000001424 substituent group Chemical group 0.000 description 7
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 6
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 6
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
108010009736 Protein Hydrolysates Proteins 0.000 description 6
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
229940048053 acrylate Drugs 0.000 description 6
239000013543 active substance Substances 0.000 description 6
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 6
235000019437 butane-1,3-diol Nutrition 0.000 description 6
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 6
238000004040 coloring Methods 0.000 description 6
230000003766 combability Effects 0.000 description 6
229920006037 cross link polymer Polymers 0.000 description 6
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 6
150000004665 fatty acids Chemical class 0.000 description 6
150000002191 fatty alcohols Chemical class 0.000 description 6
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 6
239000002736 nonionic surfactant Substances 0.000 description 6
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
229920000036 polyvinylpyrrolidone Polymers 0.000 description 6
239000003531 protein hydrolysate Substances 0.000 description 6
239000004094 surface-active agent Substances 0.000 description 6
PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 5
125000003342 alkenyl group Chemical group 0.000 description 5
125000003277 amino group Chemical group 0.000 description 5
125000004432 carbon atom Chemical group C* 0.000 description 5
230000037308 hair color Effects 0.000 description 5
125000000623 heterocyclic group Chemical group 0.000 description 5
150000002431 hydrogen Chemical class 0.000 description 5
125000002768 hydroxyalkyl group Chemical group 0.000 description 5
150000002475 indoles Chemical class 0.000 description 5
150000002476 indolines Chemical class 0.000 description 5
MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 5
125000004433 nitrogen atom Chemical group N* 0.000 description 5
229920001296 polysiloxane Polymers 0.000 description 5
229920002451 polyvinyl alcohol Polymers 0.000 description 5
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229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 description 5
238000012360 testing method Methods 0.000 description 5
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 4
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 4
NJZCRXQWPNNJNB-UHFFFAOYSA-N 2-[2-nitro-4-(trifluoromethyl)anilino]ethanol Chemical compound OCCNC1=CC=C(C(F)(F)F)C=C1[N+]([O-])=O NJZCRXQWPNNJNB-UHFFFAOYSA-N 0.000 description 4
IQXUIDYRTHQTET-UHFFFAOYSA-N 4-amino-3-nitrophenol Chemical compound NC1=CC=C(O)C=C1[N+]([O-])=O IQXUIDYRTHQTET-UHFFFAOYSA-N 0.000 description 4
KIEGFAYDOKCBOK-UHFFFAOYSA-N 6-hydroxy-4,5-dimethyl-1h-pyridin-2-one Chemical compound CC1=CC(=O)NC(O)=C1C KIEGFAYDOKCBOK-UHFFFAOYSA-N 0.000 description 4
GHVHDYYKJYXFGU-UHFFFAOYSA-N Beta-Orcinol Chemical compound CC1=CC(O)=C(C)C(O)=C1 GHVHDYYKJYXFGU-UHFFFAOYSA-N 0.000 description 4
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MIWUTEVJIISHCP-UHFFFAOYSA-N HC Blue No. 2 Chemical compound OCCNC1=CC=C(N(CCO)CCO)C=C1[N+]([O-])=O MIWUTEVJIISHCP-UHFFFAOYSA-N 0.000 description 4
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RFQSMLBZXQOMKK-UHFFFAOYSA-N [3-[(4,8-diamino-6-bromo-1,5-dioxonaphthalen-2-yl)amino]phenyl]-trimethylazanium;chloride Chemical compound [Cl-].C[N+](C)(C)C1=CC=CC(NC=2C(C3=C(N)C=C(Br)C(=O)C3=C(N)C=2)=O)=C1 RFQSMLBZXQOMKK-UHFFFAOYSA-N 0.000 description 4
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239000003093 cationic surfactant Substances 0.000 description 4
125000001309 chloro group Chemical group Cl* 0.000 description 4
HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 4
239000002537 cosmetic Substances 0.000 description 4
239000006071 cream Substances 0.000 description 4
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229910052731 fluorine Inorganic materials 0.000 description 4
229930182830 galactose Natural products 0.000 description 4
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
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VGSVNUGKHOVSPK-UHFFFAOYSA-N leukoaminochrome Chemical compound C1=C(O)C(O)=CC2=C1NCC2 VGSVNUGKHOVSPK-UHFFFAOYSA-N 0.000 description 4
238000005259 measurement Methods 0.000 description 4
OENHRRVNRZBNNS-UHFFFAOYSA-N naphthalene-1,8-diol Chemical compound C1=CC(O)=C2C(O)=CC=CC2=C1 OENHRRVNRZBNNS-UHFFFAOYSA-N 0.000 description 4
230000007935 neutral effect Effects 0.000 description 4
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 4
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LDIJKUBTLZTFRG-UHFFFAOYSA-N pyrazolo[1,5-a]pyrimidine Chemical compound N1=CC=CN2N=CC=C21 LDIJKUBTLZTFRG-UHFFFAOYSA-N 0.000 description 4
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239000002994 raw material Substances 0.000 description 4
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DWKARHJHPSUOBW-UHFFFAOYSA-N trimethyl-[3-[(2e)-2-(3-methyl-5-oxo-1-phenylpyrazol-4-ylidene)hydrazinyl]phenyl]azanium;chloride Chemical compound [Cl-].CC1=NN(C=2C=CC=CC=2)C(O)=C1N=NC1=CC=CC([N+](C)(C)C)=C1 DWKARHJHPSUOBW-UHFFFAOYSA-N 0.000 description 4
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WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 3
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CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 3
NLXFWUZKOOWWFD-UHFFFAOYSA-N 1-(2-hydroxyethylamino)-4-(methylamino)anthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(NCCO)=CC=C2NC NLXFWUZKOOWWFD-UHFFFAOYSA-N 0.000 description 3
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150000003892 tartrate salts Chemical class 0.000 description 1
235000013616 tea Nutrition 0.000 description 1
UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
239000001585 thymus vulgaris Substances 0.000 description 1
238000004448 titration Methods 0.000 description 1
230000002110 toxicologic effect Effects 0.000 description 1
231100000027 toxicology Toxicity 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
150000003626 triacylglycerols Chemical class 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
FAGMGMRSURYROS-UHFFFAOYSA-M trihexadecyl(methyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(CCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCC FAGMGMRSURYROS-UHFFFAOYSA-M 0.000 description 1
AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
229940116269 uric acid Drugs 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
235000008979 vitamin B4 Nutrition 0.000 description 1
239000011579 vitamin B4 Substances 0.000 description 1
150000003722 vitamin derivatives Chemical class 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000001993 wax Substances 0.000 description 1
229940118846 witch hazel Drugs 0.000 description 1
PEAGNRWWSMMRPZ-UHFFFAOYSA-L woodstain scarlet Chemical compound [Na+].[Na+].OC1=CC=C2C=C(S([O-])(=O)=O)C=C(S([O-])(=O)=O)C2=C1N=NC(C=C1)=CC=C1N=NC1=CC=CC=C1 PEAGNRWWSMMRPZ-UHFFFAOYSA-L 0.000 description 1
210000002268 wool Anatomy 0.000 description 1
OIHZGFWAMWHYPA-UHFFFAOYSA-N xanthylium Chemical compound C1=CC=CC2=CC3=CC=CC=C3[O+]=C21 OIHZGFWAMWHYPA-UHFFFAOYSA-N 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
239000001841 zingiber officinale Substances 0.000 description 1
239000002888 zwitterionic surfactant Substances 0.000 description 1

Classifications

- 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
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
- 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
- A61K8/34—Alcohols
- A61K8/345—Alcohols 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
- A61K8/72—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
- A61K8/817—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 a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)

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)
Emergency Medicine (AREA)
Cosmetics (AREA)

DE200910046196 2009-10-30 2009-10-30 Tönungsmittel Withdrawn DE102009046196A1 (de)

Priority Applications (2)

Application Number	Priority Date	Filing Date	Title
DE200910046196 DE102009046196A1 (de)	2009-10-30	2009-10-30	Tönungsmittel
PCT/EP2010/064969 WO2011051087A1 (fr)	2009-10-30	2010-10-07	Agent de coloration

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE200910046196 DE102009046196A1 (de)	2009-10-30	2009-10-30	Tönungsmittel

Publications (1)

Publication Number	Publication Date
DE102009046196A1 true DE102009046196A1 (de)	2011-05-05

Family

ID=43757850

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE200910046196 Withdrawn DE102009046196A1 (de)	2009-10-30	2009-10-30	Tönungsmittel

Country Status (2)

Country	Link
DE (1)	DE102009046196A1 (fr)
WO (1)	WO2011051087A1 (fr)

Citations (1)

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EP0998908A2 (fr)	1998-11-04	2000-05-10	L'oreal	Composition tinctoriale contenant un colorant direct cationique et une pyrazolo-(1,5-a)-pyrimidine à titre de base d'oxydation, et procédés de teinture

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US3986825A (en) *	1972-06-29	1976-10-19	The Gillette Company	Hair coloring composition containing water-soluble amino and quaternary ammonium polymers
DE19921962C2 (de) *	1999-05-12	2003-10-23	Wella Ag	Mittel und Verfahren zum oxidativen Färben von Haaren
JP3638490B2 (ja) *	2000-01-07	2005-04-13	花王株式会社	染色毛髪用処理組成物
FR2870732B1 (fr) *	2004-05-28	2008-05-30	Oreal	Composition pour le traitement de matieres keratiniques comprenantun compose polycarboxylique particulier et un polymere cationique et procedes la mettant en oeuvre
DE102005028623A1 (de) *	2005-06-20	2007-01-04	Henkel Kgaa	Haarpflegemittel
JP5363703B2 (ja) *	2006-06-07	2013-12-11	花王株式会社	一剤式染毛剤組成物
FR2923389B1 (fr) *	2007-11-09	2009-11-27	Oreal	Composition de teinture d'oxydation des fibres keratiniques comprenant une cellulose a substituant(s) hydrophobe(s), un colorant d'oxydation et un polymere cationique
JP5629063B2 (ja) *	2009-06-01	2014-11-19	ホーユー株式会社	毛髪化粧料組成物

2009
- 2009-10-30 DE DE200910046196 patent/DE102009046196A1/de not_active Withdrawn
2010
- 2010-10-07 WO PCT/EP2010/064969 patent/WO2011051087A1/fr not_active Ceased

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0998908A2 (fr)	1998-11-04	2000-05-10	L'oreal	Composition tinctoriale contenant un colorant direct cationique et une pyrazolo-(1,5-a)-pyrimidine à titre de base d'oxydation, et procédés de teinture

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
Hugo Janistyn, Handbuch der Kosmetika und Riechstoffe, III. Band: Die Körperpflegemittel, 2. Auflage, Dr. Alfred Hüthig Verlag Heidelberg, 1973, Seiten 68-78
Hugo Janistyn, Taschenbuch der modernen Parfümerie und Kosmetik, 4. Auflage, Wissenschaftliche Verlagsgesellschaft m. b. H. Stuttgart, 1974, Seiten 466-474
Kh. Schrader, Grundlagen und Rezepturen der Kosmetika, 2. Auflage, Hüthig Buch Verlag, Heidelberg, 1989

Also Published As

Publication number	Publication date
WO2011051087A1 (fr)	2011-05-05

Publication	Publication Date	Title
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DE102007047685A1 (de)	2008-07-31	Aufhellmittel mit kationischen Acylpyridiniumderivaten, Imidazolderivaten und Wasserstoffperoxid
DE102008046433A1 (de)	2010-03-11	Aufhellmittel mit 2-Acylpyridinium-Derivaten
DE102009028593A1 (de)	2011-02-24	Oxidative Färbemittel
DE102008032208A1 (de)	2010-01-14	Oxidationsfärbemittel mit basischer Aminosäure, Ammoniumsulfat und Alkanolaminen
DE102007019370A1 (de)	2008-10-30	Färbeverfahren mit verkürzter Anwendungszeit
DE102008044714A1 (de)	2010-03-04	Kationische Dihydroisochinolinium-Derivate als Bleichaktivatoren
DE102008036535A1 (de)	2010-02-11	Coloration mit kationisierbaren Polymer
DE102008032178A1 (de)	2010-01-21	Oxidationsfärbemittel mit Gelbasis aus hochethoxylierten Fettalkoholen und polysaccharidischem Verdicker für pH-reduzierte Expressfärbung
EP2054021A2 (fr)	2009-05-06	Colorant capillaire avec huile et hydrolysat de protéines
WO2009019048A2 (fr)	2009-02-12	Teinture pour cheveux
DE102008061855A1 (de)	2010-04-29	Mittel zum Färben von keratinhaltigen Fasern
EP2167030A2 (fr)	2010-03-31	Agents contenant un principe actif anti-irritant
WO2009027112A1 (fr)	2009-03-05	Produits de traitement capillaire
DE102010001360A1 (de)	2011-05-19	Schaumförmige Färbemittel
DE102009027485A1 (de)	2011-01-13	Schaumförmige Färbemittel
DE102010038714A1 (de)	2011-06-01	Neue Entwicklerkomponenten für die oxidative Haarfärbung mit kationischer Gruppierung des 1,4-Diazabicyclo[2.2.2]octans
DE102007053950A1 (de)	2009-05-14	Mittel mit Bioflavonoid
DE102007027862A1 (de)	2008-12-24	Verfahren zur Abfüllung haarfarbverändernder Mittel
DE102008038138A1 (de)	2010-02-25	Farbige Haarbehandlungsmittel
DE102009028523A1 (de)	2011-02-17	Schaumförmige Färbemittel II
WO2009010367A2 (fr)	2009-01-22	Agents contenant un principe actif anti-irritant
DE102008061863A1 (de)	2010-04-29	Verfahren zur Kaschierung grauer Haare
EP2173314B1 (fr)	2014-07-23	Solution vaporisable et procédé de coloration
DE102008056811A1 (de)	2009-09-17	Neue Oxidationsfarbstoffvorprodukte

Legal Events

Date	Code	Title	Description
2013-08-08	R119	Application deemed withdrawn, or ip right lapsed, due to non-payment of renewal fee	Effective date: 20130501