FI73594B - Saett foer permanentformning av haoraotervaexten och medel foer genomfoerande av detta. - Google Patents
Saett foer permanentformning av haoraotervaexten och medel foer genomfoerande av detta. Download PDFInfo
- Publication number
- FI73594B FI73594B FI843371A FI843371A FI73594B FI 73594 B FI73594 B FI 73594B FI 843371 A FI843371 A FI 843371A FI 843371 A FI843371 A FI 843371A FI 73594 B FI73594 B FI 73594B
- Authority
- FI
- Finland
- Prior art keywords
- acid
- agent
- hair
- process according
- pretreatment agent
- Prior art date
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- 210000004209 hair Anatomy 0.000 claims abstract description 81
- 238000000034 method Methods 0.000 claims abstract description 32
- 239000000126 substance Substances 0.000 claims abstract description 30
- 239000007788 liquid Substances 0.000 claims abstract description 16
- 239000002253 acid Substances 0.000 claims abstract description 13
- 229920000642 polymer Polymers 0.000 claims abstract description 11
- 125000002843 carboxylic acid group Chemical group 0.000 claims abstract description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 119
- 239000007864 aqueous solution Substances 0.000 claims description 23
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 22
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 21
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 17
- 239000002244 precipitate Substances 0.000 claims description 17
- 229920006318 anionic polymer Polymers 0.000 claims description 15
- 229920001169 thermoplastic Polymers 0.000 claims description 15
- 239000004416 thermosoftening plastic Substances 0.000 claims description 15
- 229920006317 cationic polymer Polymers 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 12
- 230000002378 acidificating effect Effects 0.000 claims description 11
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 9
- 235000010443 alginic acid Nutrition 0.000 claims description 8
- 229920000615 alginic acid Polymers 0.000 claims description 8
- 239000003638 chemical reducing agent Substances 0.000 claims description 8
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 claims description 8
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 8
- 230000007935 neutral effect Effects 0.000 claims description 8
- 238000003856 thermoforming Methods 0.000 claims description 8
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 claims description 8
- 229920001519 homopolymer Polymers 0.000 claims description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 6
- 229920001661 Chitosan Polymers 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 5
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 5
- 239000000783 alginic acid Substances 0.000 claims description 5
- 229960001126 alginic acid Drugs 0.000 claims description 5
- 150000004781 alginic acids Chemical class 0.000 claims description 5
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 claims description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 4
- LCQXXBOSCBRNNT-UHFFFAOYSA-K ammonium aluminium sulfate Chemical compound [NH4+].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O LCQXXBOSCBRNNT-UHFFFAOYSA-K 0.000 claims description 4
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 claims description 4
- 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 claims description 4
- 239000004310 lactic acid Substances 0.000 claims description 4
- 235000014655 lactic acid Nutrition 0.000 claims description 4
- 125000005397 methacrylic acid ester group Chemical group 0.000 claims description 4
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 3
- 125000005396 acrylic acid ester group Chemical group 0.000 claims description 3
- 159000000007 calcium salts Chemical class 0.000 claims description 3
- 229910017053 inorganic salt Inorganic materials 0.000 claims description 3
- 239000000178 monomer Substances 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 claims description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 2
- 235000011054 acetic acid Nutrition 0.000 claims description 2
- HDYRYUINDGQKMC-UHFFFAOYSA-M acetyloxyaluminum;dihydrate Chemical compound O.O.CC(=O)O[Al] HDYRYUINDGQKMC-UHFFFAOYSA-M 0.000 claims description 2
- 229940072056 alginate Drugs 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 229940009827 aluminum acetate Drugs 0.000 claims description 2
- 150000001413 amino acids Chemical class 0.000 claims description 2
- HKVFISRIUUGTIB-UHFFFAOYSA-O azanium;cerium;nitrate Chemical compound [NH4+].[Ce].[O-][N+]([O-])=O HKVFISRIUUGTIB-UHFFFAOYSA-O 0.000 claims description 2
- 235000015165 citric acid Nutrition 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 235000021317 phosphate Nutrition 0.000 claims description 2
- 235000011007 phosphoric acid Nutrition 0.000 claims description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 239000011975 tartaric acid Substances 0.000 claims description 2
- 235000002906 tartaric acid Nutrition 0.000 claims description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
- 229920002554 vinyl polymer Polymers 0.000 claims description 2
- 239000000499 gel Substances 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 26
- 238000007493 shaping process Methods 0.000 abstract description 9
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 abstract description 3
- 239000003921 oil Substances 0.000 description 12
- 239000002304 perfume Substances 0.000 description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
- 239000000834 fixative Substances 0.000 description 10
- 239000007800 oxidant agent Substances 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- 230000003779 hair growth Effects 0.000 description 9
- IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 8
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 7
- 239000006185 dispersion Substances 0.000 description 7
- 230000001590 oxidative effect Effects 0.000 description 7
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
- 239000001099 ammonium carbonate Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 229910021529 ammonia Inorganic materials 0.000 description 5
- XUXNAKZDHHEHPC-UHFFFAOYSA-M sodium bromate Chemical compound [Na+].[O-]Br(=O)=O XUXNAKZDHHEHPC-UHFFFAOYSA-M 0.000 description 5
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 5
- PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 102000011782 Keratins Human genes 0.000 description 4
- 108010076876 Keratins Proteins 0.000 description 4
- ZZTCCAPMZLDHFM-UHFFFAOYSA-N ammonium thioglycolate Chemical compound [NH4+].[O-]C(=O)CS ZZTCCAPMZLDHFM-UHFFFAOYSA-N 0.000 description 4
- 235000013871 bee wax Nutrition 0.000 description 4
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- -1 mercapto compounds Chemical class 0.000 description 4
- SASYHUDIOGGZCN-ARJAWSKDSA-N (z)-2-ethylbut-2-enedioic acid Chemical compound CC\C(C(O)=O)=C\C(O)=O SASYHUDIOGGZCN-ARJAWSKDSA-N 0.000 description 3
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 3
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
- 239000004141 Sodium laurylsulphate Substances 0.000 description 3
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 3
- 235000012501 ammonium carbonate Nutrition 0.000 description 3
- 229940075861 ammonium thioglycolate Drugs 0.000 description 3
- 239000013065 commercial product Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 229920002521 macromolecule Polymers 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 238000002203 pretreatment Methods 0.000 description 3
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 3
- 229940035044 sorbitan monolaurate Drugs 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
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- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000003929 acidic solution Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- POJWUDADGALRAB-UHFFFAOYSA-N allantoin Chemical compound NC(=O)NC1NC(=O)NC1=O POJWUDADGALRAB-UHFFFAOYSA-N 0.000 description 2
- VHFSMDHANDABQK-UHFFFAOYSA-N azane;2-sulfanylpropanoic acid Chemical compound [NH4+].CC(S)C([O-])=O VHFSMDHANDABQK-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000003349 gelling agent Substances 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
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- 229910052742 iron Inorganic materials 0.000 description 2
- 235000019388 lanolin Nutrition 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
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- 230000003472 neutralizing effect Effects 0.000 description 2
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- 238000002360 preparation method Methods 0.000 description 2
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- 102000004169 proteins and genes Human genes 0.000 description 2
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- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 2
- XVOUMQNXTGKGMA-OWOJBTEDSA-N (E)-glutaconic acid Chemical compound OC(=O)C\C=C\C(O)=O XVOUMQNXTGKGMA-OWOJBTEDSA-N 0.000 description 1
- 239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 description 1
- DBTKYUOIYBJHKK-XQRVVYSFSA-N (z)-2-(2-methylpropyl)but-2-enedioic acid Chemical compound CC(C)C\C(C(O)=O)=C\C(O)=O DBTKYUOIYBJHKK-XQRVVYSFSA-N 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- NJMGRJLQRLFQQX-HYXAFXHYSA-N 2-isopropylmaleic acid Chemical compound CC(C)C(\C(O)=O)=C\C(O)=O NJMGRJLQRLFQQX-HYXAFXHYSA-N 0.000 description 1
- JKGHDBJDBRBRNA-UHFFFAOYSA-N 2-methylpent-2-enedioic acid Chemical compound OC(=O)C(C)=CCC(O)=O JKGHDBJDBRBRNA-UHFFFAOYSA-N 0.000 description 1
- XWNSFEAWWGGSKJ-UHFFFAOYSA-N 4-acetyl-4-methylheptanedinitrile Chemical compound N#CCCC(C)(C(=O)C)CCC#N XWNSFEAWWGGSKJ-UHFFFAOYSA-N 0.000 description 1
- HRSYWPMGIIAQIW-UHFFFAOYSA-N 5-bromo-2,3-dihydro-1,4-benzodioxine-7-carbaldehyde Chemical compound O1CCOC2=C1C=C(C=O)C=C2Br HRSYWPMGIIAQIW-UHFFFAOYSA-N 0.000 description 1
- DEXFNLNNUZKHNO-UHFFFAOYSA-N 6-[3-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-3-oxopropyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)C(CCC1=CC2=C(NC(O2)=O)C=C1)=O DEXFNLNNUZKHNO-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
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- DCXYFEDJOCDNAF-UHFFFAOYSA-N Asparagine Natural products OC(=O)C(N)CC(N)=O DCXYFEDJOCDNAF-UHFFFAOYSA-N 0.000 description 1
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- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
- PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 description 1
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- 239000004471 Glycine Substances 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
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- 229930195722 L-methionine Natural products 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
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- 239000005662 Paraffin oil Substances 0.000 description 1
- 239000004153 Potassium bromate Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229940091181 aconitic acid Drugs 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
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- 239000003513 alkali Substances 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
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- 229910001617 alkaline earth metal chloride Inorganic materials 0.000 description 1
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- 229960000458 allantoin Drugs 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
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- 230000002579 anti-swelling effect Effects 0.000 description 1
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- OKHHGHGGPDJQHR-YMOPUZKJSA-L calcium;(2s,3s,4s,5s,6r)-6-[(2r,3s,4r,5s,6r)-2-carboxy-6-[(2r,3s,4r,5s,6r)-2-carboxylato-4,5,6-trihydroxyoxan-3-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate Chemical compound [Ca+2].O[C@@H]1[C@H](O)[C@H](O)O[C@@H](C([O-])=O)[C@H]1O[C@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@H](O2)C([O-])=O)O)[C@H](C(O)=O)O1 OKHHGHGGPDJQHR-YMOPUZKJSA-L 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 239000000490 cosmetic additive Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 235000018417 cysteine Nutrition 0.000 description 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 1
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- UXYBXUYUKHUNOM-UHFFFAOYSA-M ethyl(trimethyl)azanium;chloride Chemical compound [Cl-].CC[N+](C)(C)C UXYBXUYUKHUNOM-UHFFFAOYSA-M 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 229960002989 glutamic acid Drugs 0.000 description 1
- DOGJSOZYUGJVKS-UHFFFAOYSA-N glyceryl monothioglycolate Chemical compound OCC(O)COC(=O)CS DOGJSOZYUGJVKS-UHFFFAOYSA-N 0.000 description 1
- 230000003700 hair damage Effects 0.000 description 1
- 210000003780 hair follicle Anatomy 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 235000000396 iron Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
- 229960004452 methionine Drugs 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
- PJUIMOJAAPLTRJ-UHFFFAOYSA-N monothioglycerol Chemical class OCC(O)CS PJUIMOJAAPLTRJ-UHFFFAOYSA-N 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 208000005833 pili torti Diseases 0.000 description 1
- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 description 1
- 229940094037 potassium bromate Drugs 0.000 description 1
- 235000019396 potassium bromate Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- XTUSEBKMEQERQV-UHFFFAOYSA-N propan-2-ol;hydrate Chemical compound O.CC(C)O XTUSEBKMEQERQV-UHFFFAOYSA-N 0.000 description 1
- UORVCLMRJXCDCP-UHFFFAOYSA-N propynoic acid Chemical compound OC(=O)C#C UORVCLMRJXCDCP-UHFFFAOYSA-N 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- CRWJEUDFKNYSBX-UHFFFAOYSA-N sodium;hypobromite Chemical compound [Na+].Br[O-] CRWJEUDFKNYSBX-UHFFFAOYSA-N 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-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
- A61K8/81—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)
- A61K8/8182—Copolymers of vinyl-pyrrolidones. Compositions of derivatives of such polymers
-
- 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
- A61K8/73—Polysaccharides
- A61K8/736—Chitin; Chitosan; 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8147—Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
-
- 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)
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Cosmetics (AREA)
- Hair Curling (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Measurement And Recording Of Electrical Phenomena And Electrical Characteristics Of The Living Body (AREA)
- Eye Examination Apparatus (AREA)
- Control Of Combustion (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Surface Acoustic Wave Elements And Circuit Networks Thereof (AREA)
- Physical Deposition Of Substances That Are Components Of Semiconductor Devices (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Moulding By Coating Moulds (AREA)
- Reinforced Plastic Materials (AREA)
Claims (17)
1. Förfarande för selektiv permanentformning av här-efterväxten, varvid man först behandlar häret med ett fly- 5 tande, vattenhaltigt förbehandlingsmedel, rullar pa pa il-jotter, behandlar med ett vattenhaltigt, reducerande permanent formningsmedel , spolar, fixerar oxidativt och sedan vi-darebehandlar pä ett sedvanligt sätt, känneteck-n a t därav, att man väljer för behandlingsmedlet och per-10 manentformningsmedlet sä, att dessa vid kontakt med varandra pä kontaktytan bildar ett separerande skikt, vilket försvä-rar eller förhindrar blandandet mellan förbehandlingsmedlet och permanentformningsmedlet.
2. Förfarande enligt patentkravet 1, känne-15 tecknat därav, att man som förbehandlingsmedel an- vänder en flytande, vattenhaltig komposition, vilken innehäller ätminstone ett fysiologiskt fördragbart material, vilket är lösligt eller dispergerbart i en svagt sur eller neutral vattenlösning och vilket vid ett svagt alkaliskt 20 pH-värde bildar en gel eller en fällning, varefter man an-vänder ett vattenhaltigt, reducerande permanentformnings-medel med ett pH av 7,5-11.
3. Förfarande enligt patentkravet 2, känne-tecknat därav, att man använder ett förbehandlings- 25 medel, vilket innehäller minst en fysiologiskt fördragbar, naturlig eller syntetisk polykarboxylsyrapolymer, vilken helt eller delvis uppbyggts av monomerenheter som innehäl-ler en fri karboxylgrupp.
4. Förfarande enligt patentkravet 3, känne-30 tecknat därav, att man använder ett förbehandlingsmedel, vilket innehäller alginsyra eller en fysiologiskt fördragbar, högpolymeriserad homopolymer av akrylsyra eller metakrylsyra.
5. Förfarande enligt patentkravet 3, känne-35 tecknat därav, att man använder ett förbehandlingsmedel, vilket innehäller ett högpolymeriserat sam- eller blandpolymerisat av akrylsyra och/eller metakrylsyra med akrylsyra- eller metakry.l syraestrar, akrylsyra- eller 22 73594 metakrylsyraamider, akrylsyra- eller metakrylsyraimider, krotonsyra, vinylacetat, styren eller andra vinyl- eller allylderivat, varvid minst 25 mol-% av polymerisatet bestär av enheter som innehäller karboxylsyragrupper. 5
6. Förfarande enligt patentkravet 3, kanne- t e c k n a t därav, att man använder ett förbehandlings-medel, vilket innehaller ett högmolekulärt sampolymerisat av akrylsyra och metaksylsyra eller akrylsyra och akrylsy-raester eller akrylsyra och metakrylsyraester eller metak-10 rylsyra och akrylsyraester eller metakrylsyra och metakrylsyraester, varvid de nämnda estrarna isynnerhet bestar av metyl-, etyl-, propyl- eller butylestrar.
7. Förfarande enligt patentkravet 2, känne-t e c k n a t därav, att man som förbehandlingsmedel an-15 vänder en komposition, vilken innehäller ätminstone ett fysiologiskt fördragbart, organiskt eller oorganiskt sait, vilket är lösligt eller dispergerbart i en svagt sur eller neutral vattenlösning och vilket vid ett svagt alkaliskt pH-värde bildar en gel eller en fällning. 20
8. Förfarande enligt patentkravet 7, känne- t e c k n a t därav, att man som fysiologiskt fördragbart, organiskt eller oorganiskt sait använder aluminiumacetat, ammoniumaluminiumsulfat eller ammoniumceriumnitrat.
9. Förfarande enligt patentkravet 7, känne-25 tecknat därav, att man som förbehandlingsmedel använder en komposition, vilken innehäller ett vattenlösligt, fysiologiskt fördragbart sait av chitosan.
10. Förfarande enligt nägot av patentkraven 2-9, kännetecknat därav, att man använder ett förbe- 30 handlingsmedel, vilket innehaller det fysiologiskt fördrag-bara materialet som är lösligt eller dispergerbart i en svagt sur eller neutral vattenlösning och som vid ett svagt alkaliskt pH-värde bildar en gel eller en fällning, i en mängd av 1-10 vikt-%. 35
11. Förfarande enligt patentkravet 1, känne tecknat därav, att man som förbehandlingsmedel använder en vattenhaltig komposition, som innehäller algin-
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3301515 | 1983-01-19 | ||
| DE3301515A DE3301515A1 (de) | 1983-01-19 | 1983-01-19 | Verfahren zur dauerverformung des haarnachwuchses und mittel zu seiner durchfuehrung |
| PCT/EP1983/000350 WO1984002842A1 (en) | 1983-01-19 | 1983-12-29 | Permanent wave process for recently grown hair and means for implementing the process |
| EP8300350 | 1983-12-29 |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| FI843371A FI843371A (fi) | 1984-08-27 |
| FI843371A0 FI843371A0 (fi) | 1984-08-27 |
| FI73594B true FI73594B (fi) | 1987-07-31 |
| FI73594C FI73594C (sv) | 1987-11-09 |
Family
ID=6188544
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI843371A FI73594C (sv) | 1983-01-19 | 1984-08-27 | Sätt för permanentformning av håråterväxten och medel för genomförande av detta. |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4660580A (sv) |
| EP (1) | EP0114414B1 (sv) |
| AT (1) | ATE34656T1 (sv) |
| AU (1) | AU563116B2 (sv) |
| CA (1) | CA1216242A (sv) |
| DE (2) | DE3301515A1 (sv) |
| DK (1) | DK164475C (sv) |
| ES (1) | ES8503505A1 (sv) |
| FI (1) | FI73594C (sv) |
| MX (1) | MX159030A (sv) |
| PT (1) | PT77903B (sv) |
| WO (1) | WO1984002842A1 (sv) |
| ZA (1) | ZA84355B (sv) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL8601762A (nl) * | 1986-07-07 | 1988-02-01 | Bouke Jan Lange | Werkwijze voor de reiniging en conditionering en eventuele medicinale behandeling van het haar en de hoofdhuid, een voor dit doel bruikbare tweefasen shampoo, alsmede een verpakking daarvoor. |
| DE3627746A1 (de) * | 1986-08-16 | 1988-02-18 | Henkel Kgaa | Verfahren zur dauerhaften haarverformung |
| US4709712A (en) * | 1986-10-22 | 1987-12-01 | Dermatalogical Products Of Texas | Polycarboxylic acid polymer gels as protective agents |
| US4832947A (en) * | 1987-03-27 | 1989-05-23 | A-Veda Corporation | Process of incorporating essential oils into hair fibers and permanent waving process and compositions therefor |
| US5116606A (en) * | 1989-03-09 | 1992-05-26 | Alt John P | Skin treatment method and solution |
| US5116605A (en) * | 1989-03-09 | 1992-05-26 | Alt John P | Composition and skin treatment method therewith for mitigating acne and male-pattern baldness |
| US5090428A (en) * | 1989-07-20 | 1992-02-25 | International Packagers, Inc. | Protein coated hair protection apparatus and method |
| US6699261B1 (en) * | 1992-01-07 | 2004-03-02 | Cch Associates, Inc. | Blood vessel sealing system |
| JP3148365B2 (ja) † | 1992-06-29 | 2001-03-19 | 花王株式会社 | ケラチン質繊維改質剤キット |
| US5348737A (en) * | 1993-07-21 | 1994-09-20 | Avlon Industries, Inc. | Composition and process for decreasing hair fiber swelling |
| DE4325817A1 (de) * | 1993-07-31 | 1995-02-02 | Wella Ag | Haarbehandlungsmittel und Verfahren zur Anwendung |
| FR2708602B1 (fr) * | 1993-08-02 | 1995-10-06 | Oreal | Procédé d'extraction des composés malodorants présents dans une formulation contenant au moins un composé comportant un groupe thiol et compositions désodorisées ainsi obtenues. |
| FR2721823B1 (fr) * | 1994-06-30 | 1996-08-02 | Oreal | Procede pour la deformation permanente des matieres keratiniques |
| US5988180A (en) * | 1994-12-22 | 1999-11-23 | Zotos International, Inc. | Leave-on oxidizing solution for permanent waving of hair and a process for permanent waving of hair |
| US6116250A (en) * | 1996-07-20 | 2000-09-12 | Wella Aktiengesellschaft | Process of permanent hair shaping |
| FR2755364B1 (fr) * | 1996-11-06 | 1999-01-22 | Eugene Perma Sa | Composition pour la deformation permanente des fibres keratiniques, obtention et mise en oeuvre |
| FR2778560B1 (fr) | 1998-05-12 | 2001-06-01 | Oreal | Utilisation de l'acide cinnamique ou d'au moins l'un de ses derives dans une composition destinee a favoriser la desquamation de la peau, et composition le comprenant |
| FR2795316B1 (fr) * | 1999-06-28 | 2004-12-24 | Oreal | Procede de permanente comprenant l'application preliminaire d'une composition comprenant au moins un polymere anionique |
| FR2795635B1 (fr) | 1999-06-30 | 2006-09-15 | Oreal | Mascara comprenant des polymeres filmogenes |
| CA2484927C (en) * | 2002-05-17 | 2009-01-27 | Halliburton Energy Services, Inc. | Method and apparatus for mwd formation testing |
| US20040113394A1 (en) * | 2002-12-11 | 2004-06-17 | Pao-Hsien Cheng | Supporting mechanism of a foldable stroller |
| FR2858552B1 (fr) * | 2004-05-14 | 2006-03-03 | Oreal | Procede de deformation permanente des cheveux comprenant une etape de precipitation in situ d'un polymere anionique ou amphotere |
| FR2858551B1 (fr) * | 2003-08-07 | 2008-07-11 | Oreal | Procede de deformation permanente des cheveux comprenant une etape de precipitation in situ d'un polymere anionique ou amphotere |
| CA2475435A1 (fr) * | 2003-08-07 | 2005-02-07 | L'oreal | Procede de deformation permanente des cheveux comprenant une etape de precipitation in situ d'un polymere anionique ou amphotere |
| US20050074418A1 (en) * | 2003-08-07 | 2005-04-07 | Catherine Campain | Process for permanently reshaping the hair, comprising a step of in situ precipitation of an anionic or amphoteric polymer |
| US7824664B2 (en) * | 2005-04-29 | 2010-11-02 | L'oreal S.A. | Semipermanent hair shaping method |
| FR2885041B1 (fr) * | 2005-04-29 | 2009-07-03 | Oreal | Procede de mise en forme semi-permanente des cheveux |
| FR2885040B1 (fr) | 2005-04-29 | 2008-12-26 | Oreal | Procede de mise en forme semi-permanente des cheveux |
| US7744859B2 (en) * | 2005-04-29 | 2010-06-29 | L'oreal S.A. | Semipermanent hair shaping method |
| DE102015226174A1 (de) * | 2015-12-21 | 2017-06-22 | Henkel Ag & Co. Kgaa | Geruchsreduziertes Verfahren zur permanenten Umformung von Keratinfasern |
| DE102015226170A1 (de) * | 2015-12-21 | 2017-06-22 | Henkel Ag & Co. Kgaa | Geruchsreduzierte Blondierung mit flüssiger Strähnenfolie |
| EP3238693B1 (en) | 2016-04-25 | 2022-10-19 | Wella Operations US, LLC | Hair treatment method and kit thereof |
| EP3448525A1 (en) * | 2016-04-25 | 2019-03-06 | Noxell Corporation | Method for colouring hair including pretreatment |
| WO2022223778A1 (en) * | 2021-04-23 | 2022-10-27 | Helmholtz-Zentrum für Infektionsforschung GmbH | Citraconic acid and derivatives thereof for use as a medicament |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1239062B (de) * | 1963-08-14 | 1967-04-20 | Schwarzkopf Fa Hans | Verfahren zur Haarverfestigung |
| JPS5555109A (en) * | 1978-10-20 | 1980-04-22 | Nippon Oil & Fats Co Ltd | Cold-wave lotion |
| JPS57144213A (en) * | 1981-03-03 | 1982-09-06 | Kao Corp | Hair treatment |
-
1983
- 1983-01-19 DE DE3301515A patent/DE3301515A1/de not_active Withdrawn
- 1983-12-29 WO PCT/EP1983/000350 patent/WO1984002842A1/de active IP Right Grant
- 1983-12-29 EP EP83113206A patent/EP0114414B1/de not_active Expired
- 1983-12-29 US US06/642,670 patent/US4660580A/en not_active Expired - Lifetime
- 1983-12-29 PT PT77903A patent/PT77903B/pt not_active IP Right Cessation
- 1983-12-29 AU AU23441/84A patent/AU563116B2/en not_active Ceased
- 1983-12-29 AT AT83113206T patent/ATE34656T1/de not_active IP Right Cessation
- 1983-12-29 DE DE8383113206T patent/DE3376796D1/de not_active Expired
-
1984
- 1984-01-17 MX MX200057A patent/MX159030A/es unknown
- 1984-01-17 ZA ZA84355A patent/ZA84355B/xx unknown
- 1984-01-18 CA CA000445524A patent/CA1216242A/en not_active Expired
- 1984-01-19 ES ES529024A patent/ES8503505A1/es not_active Expired
- 1984-08-27 FI FI843371A patent/FI73594C/sv not_active IP Right Cessation
- 1984-09-11 DK DK433284A patent/DK164475C/da active
Also Published As
| Publication number | Publication date |
|---|---|
| PT77903B (de) | 1986-04-11 |
| ATE34656T1 (de) | 1988-06-15 |
| FI843371A (fi) | 1984-08-27 |
| AU2344184A (en) | 1984-08-15 |
| ES529024A0 (es) | 1985-03-01 |
| PT77903A (de) | 1984-01-01 |
| MX159030A (es) | 1989-04-12 |
| ES8503505A1 (es) | 1985-03-01 |
| DK164475C (da) | 1992-11-23 |
| ZA84355B (en) | 1984-08-29 |
| DK433284A (da) | 1984-09-11 |
| DE3376796D1 (en) | 1988-07-07 |
| DE3301515A1 (de) | 1984-07-19 |
| FI843371A0 (fi) | 1984-08-27 |
| AU563116B2 (en) | 1987-06-25 |
| WO1984002842A1 (en) | 1984-08-02 |
| FI73594C (sv) | 1987-11-09 |
| DK164475B (da) | 1992-07-06 |
| EP0114414B1 (de) | 1988-06-01 |
| DK433284D0 (da) | 1984-09-11 |
| EP0114414A1 (de) | 1984-08-01 |
| CA1216242A (en) | 1987-01-06 |
| US4660580A (en) | 1987-04-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed | ||
| MM | Patent lapsed |
Owner name: WELLA AKTIENGESELLSCHAFT |