JP2017538732A5 - - Google Patents
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- JP2017538732A5 JP2017538732A5 JP2017532811A JP2017532811A JP2017538732A5 JP 2017538732 A5 JP2017538732 A5 JP 2017538732A5 JP 2017532811 A JP2017532811 A JP 2017532811A JP 2017532811 A JP2017532811 A JP 2017532811A JP 2017538732 A5 JP2017538732 A5 JP 2017538732A5
- Authority
- JP
- Japan
- Prior art keywords
- crosslinking agent
- alkyl
- monomer
- composition
- acrylate
- Prior art date
- 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.)
- Pending
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- 239000000203 mixture Substances 0.000 claims description 117
- 239000000178 monomer Substances 0.000 claims description 100
- 239000003431 cross linking reagent Substances 0.000 claims description 70
- 125000000217 alkyl group Chemical group 0.000 claims description 50
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 28
- 239000004908 Emulsion polymer Substances 0.000 claims description 24
- 229920000642 polymer Polymers 0.000 claims description 22
- 229910052739 hydrogen Inorganic materials 0.000 claims description 21
- 239000001257 hydrogen Substances 0.000 claims description 21
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 12
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 claims description 12
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 12
- 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- 125000002947 alkylene group Chemical group 0.000 claims description 11
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 claims description 10
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 10
- -1 vinyl halides Chemical class 0.000 claims description 10
- 229920002554 vinyl polymer Polymers 0.000 claims description 10
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 9
- 239000003945 anionic surfactant Substances 0.000 claims description 8
- 239000004094 surface-active agent Substances 0.000 claims description 8
- 229920001567 vinyl ester resin Polymers 0.000 claims description 8
- 208000001840 Dandruff Diseases 0.000 claims description 7
- 230000002209 hydrophobic effect Effects 0.000 claims description 7
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 6
- 239000002280 amphoteric surfactant Substances 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 229910052725 zinc Inorganic materials 0.000 claims description 6
- 239000011701 zinc Substances 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- 239000002453 shampoo Substances 0.000 claims description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 5
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 4
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 150000002148 esters Chemical group 0.000 claims description 4
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical compound NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 239000003921 oil Substances 0.000 claims description 4
- UOURRHZRLGCVDA-UHFFFAOYSA-D pentazinc;dicarbonate;hexahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Zn+2].[Zn+2].[Zn+2].[Zn+2].[Zn+2].[O-]C([O-])=O.[O-]C([O-])=O UOURRHZRLGCVDA-UHFFFAOYSA-D 0.000 claims description 4
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical group OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- JPJALAQPGMAKDF-UHFFFAOYSA-N selenium dioxide Chemical compound O=[Se]=O JPJALAQPGMAKDF-UHFFFAOYSA-N 0.000 claims description 4
- 125000005504 styryl group Chemical group 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 239000001993 wax Substances 0.000 claims description 4
- 239000002888 zwitterionic surfactant Substances 0.000 claims description 4
- 239000004971 Cross linker Substances 0.000 claims description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 125000000732 arylene group Chemical group 0.000 claims description 3
- 125000002837 carbocyclic group Chemical group 0.000 claims description 3
- FGVVTMRZYROCTH-UHFFFAOYSA-N pyridine-2-thiol N-oxide Chemical compound [O-][N+]1=CC=CC=C1S FGVVTMRZYROCTH-UHFFFAOYSA-N 0.000 claims description 3
- 229960002026 pyrithione Drugs 0.000 claims description 3
- 239000011787 zinc oxide Substances 0.000 claims description 3
- 125000006833 (C1-C5) alkylene group Chemical group 0.000 claims description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 2
- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 2
- 150000001298 alcohols Chemical class 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 2
- 239000012736 aqueous medium Substances 0.000 claims description 2
- 125000001204 arachidyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 125000002511 behenyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims description 2
- 150000001767 cationic compounds Chemical class 0.000 claims description 2
- 229920006317 cationic polymer Polymers 0.000 claims description 2
- 230000003750 conditioning effect Effects 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- WNMORWGTPVWAIB-UHFFFAOYSA-N ethenyl 2-methylpropanoate Chemical compound CC(C)C(=O)OC=C WNMORWGTPVWAIB-UHFFFAOYSA-N 0.000 claims description 2
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 claims description 2
- GFJVXXWOPWLRNU-UHFFFAOYSA-N ethenyl formate Chemical compound C=COC=O GFJVXXWOPWLRNU-UHFFFAOYSA-N 0.000 claims description 2
- BLZSRIYYOIZLJL-UHFFFAOYSA-N ethenyl pentanoate Chemical compound CCCCC(=O)OC=C BLZSRIYYOIZLJL-UHFFFAOYSA-N 0.000 claims description 2
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 150000002430 hydrocarbons Chemical class 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 150000003951 lactams Chemical group 0.000 claims description 2
- 125000002819 montanyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 claims description 2
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 2
- 125000005702 oxyalkylene group Chemical group 0.000 claims description 2
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 2
- 229920001296 polysiloxane Polymers 0.000 claims description 2
- 229960004889 salicylic acid Drugs 0.000 claims description 2
- VIDTVPHHDGRGAF-UHFFFAOYSA-N selenium sulfide Chemical compound [Se]=S VIDTVPHHDGRGAF-UHFFFAOYSA-N 0.000 claims description 2
- 229960005265 selenium sulfide Drugs 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 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 claims description 2
- MQWLIFWNJWLDCI-UHFFFAOYSA-L zinc;carbonate;hydrate Chemical compound O.[Zn+2].[O-]C([O-])=O MQWLIFWNJWLDCI-UHFFFAOYSA-L 0.000 claims description 2
- 150000003851 azoles Chemical class 0.000 claims 1
- 239000003599 detergent Substances 0.000 claims 1
- 230000001804 emulsifying effect Effects 0.000 claims 1
- GGOZGYRTNQBSSA-UHFFFAOYSA-N pyridine-2,3-diol Chemical class OC1=CC=CN=C1O GGOZGYRTNQBSSA-UHFFFAOYSA-N 0.000 claims 1
- 229940043810 zinc pyrithione Drugs 0.000 claims 1
- 229910052738 indium Inorganic materials 0.000 description 9
- 150000002170 ethers Chemical class 0.000 description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical group [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- BTBJBAZGXNKLQC-UHFFFAOYSA-N ammonium lauryl sulfate Chemical compound [NH4+].CCCCCCCCCCCCOS([O-])(=O)=O BTBJBAZGXNKLQC-UHFFFAOYSA-N 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000007046 ethoxylation reaction Methods 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 2
- WHMDPDGBKYUEMW-UHFFFAOYSA-N pyridine-2-thiol Chemical compound SC1=CC=CC=N1 WHMDPDGBKYUEMW-UHFFFAOYSA-N 0.000 description 2
- 229920005604 random copolymer Polymers 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 235000014692 zinc oxide Nutrition 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- TYMYJUHDFROXOO-UHFFFAOYSA-N 1,3-bis(prop-2-enoxy)-2,2-bis(prop-2-enoxymethyl)propane Chemical compound C=CCOCC(COCC=C)(COCC=C)COCC=C TYMYJUHDFROXOO-UHFFFAOYSA-N 0.000 description 1
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 1
- JHSWSKVODYPNDV-UHFFFAOYSA-N 2,2-bis(prop-2-enoxymethyl)propane-1,3-diol Chemical group C=CCOCC(CO)(CO)COCC=C JHSWSKVODYPNDV-UHFFFAOYSA-N 0.000 description 1
- FYRWKWGEFZTOQI-UHFFFAOYSA-N 3-prop-2-enoxy-2,2-bis(prop-2-enoxymethyl)propan-1-ol Chemical compound C=CCOCC(CO)(COCC=C)COCC=C FYRWKWGEFZTOQI-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical class [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 229940063953 ammonium lauryl sulfate Drugs 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical group CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 description 1
- 229940073507 cocamidopropyl betaine Drugs 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- BOUCRWJEKAGKKG-UHFFFAOYSA-N n-[3-(diethylaminomethyl)-4-hydroxyphenyl]acetamide Chemical compound CCN(CC)CC1=CC(NC(C)=O)=CC=C1O BOUCRWJEKAGKKG-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229960001141 pyrithione zinc Drugs 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229940057950 sodium laureth sulfate Drugs 0.000 description 1
- 229940102541 sodium trideceth sulfate Drugs 0.000 description 1
- SXHLENDCVBIJFO-UHFFFAOYSA-M sodium;2-[2-(2-dodecoxyethoxy)ethoxy]ethyl sulfate Chemical compound [Na+].CCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O SXHLENDCVBIJFO-UHFFFAOYSA-M 0.000 description 1
- KLYDBHUQNXKACI-UHFFFAOYSA-M sodium;2-[2-(2-tridecoxyethoxy)ethoxy]ethyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O KLYDBHUQNXKACI-UHFFFAOYSA-M 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 238000004876 x-ray fluorescence Methods 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462093631P | 2014-12-18 | 2014-12-18 | |
| US62/093,631 | 2014-12-18 | ||
| PCT/US2015/066021 WO2016100466A1 (en) | 2014-12-18 | 2015-12-16 | Amphiphilic suspension and stability agent for antidandruff hair care compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2017538732A JP2017538732A (ja) | 2017-12-28 |
| JP2017538732A5 true JP2017538732A5 (enExample) | 2019-01-31 |
Family
ID=55027823
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017532811A Pending JP2017538732A (ja) | 2014-12-18 | 2015-12-16 | フケ防止用ヘアケア組成物のための両親媒性懸濁安定剤 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20170367963A1 (enExample) |
| EP (1) | EP3233026A1 (enExample) |
| JP (1) | JP2017538732A (enExample) |
| KR (1) | KR20170095373A (enExample) |
| CN (1) | CN107249558A (enExample) |
| AR (1) | AR103069A1 (enExample) |
| BR (1) | BR112017012784A2 (enExample) |
| WO (1) | WO2016100466A1 (enExample) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10610473B2 (en) | 2016-03-24 | 2020-04-07 | The Procter And Gamble Company | Hair care compositions comprising malodor reduction compositions |
| DE102016219862A1 (de) * | 2016-10-12 | 2018-04-12 | Henkel Ag & Co. Kgaa | Waschmittelzusammensetzung mit Fließgrenze |
| CN110582262B (zh) | 2017-04-26 | 2023-06-23 | 联合利华知识产权控股有限公司 | 包含吡啶硫酮的抗头皮屑毛发护理组合物 |
| CN110831981B (zh) | 2017-05-04 | 2022-06-24 | 路博润先进材料公司 | 双活化微凝胶 |
| MX386122B (es) | 2017-05-12 | 2025-03-18 | Procter & Gamble | Composiciones con agentes para la salud del cuero cabelludo con depósito incrementado. |
| JP2020531533A (ja) * | 2017-08-22 | 2020-11-05 | ルブリゾル アドバンスド マテリアルズ， インコーポレイテッド | 冬期関連の掻痒を緩和するための石鹸組成物および処置方法 |
| MX388497B (es) | 2017-10-10 | 2025-03-20 | Procter & Gamble | Composición de champú compacta. |
| MX391873B (es) | 2017-11-03 | 2025-03-21 | Unilever Ip Holdings B V | Composición de champú y método de uso. |
| MX394256B (es) | 2017-11-03 | 2025-03-24 | Unilever Ip Holdings B V | Composicion anticaspa y metodo de uso |
| US11638685B2 (en) | 2017-12-08 | 2023-05-02 | Conopco, Inc. | Hair care composition |
| WO2019177925A1 (en) * | 2018-03-16 | 2019-09-19 | Lubrizol Advanced Materials, Inc. | Foaming cleanser compositions containing a non-polar oil and amphiphilic polymer |
| WO2019222338A1 (en) | 2018-05-15 | 2019-11-21 | The Procter & Gamble Company | Synergistic antioxidant compositions |
| WO2020123609A1 (en) * | 2018-12-11 | 2020-06-18 | Lubrizol Advanced Materials, Inc. | Compositions and treatment methods for the mitigation of winter season related pruritus |
| MX2021004960A (es) * | 2018-12-20 | 2021-06-15 | Procter & Gamble | Composicion para el cuidado del cuero cabelludo con estabilidad mejorada. |
| KR102809026B1 (ko) * | 2019-08-01 | 2025-05-21 | 애경산업(주) | 비듬 완화 두피 세정용 조성물 |
| BR112022010474A2 (pt) | 2019-12-06 | 2022-09-06 | Procter & Gamble | Composição isenta de sulfato com deposição acentuada de ativo sobre o couro cabeludo |
| EP4110474A1 (en) | 2020-02-27 | 2023-01-04 | The Procter & Gamble Company | Anti-dandruff compositions with sulfur having enhanced efficacy and aesthetics |
| EP4171755A1 (en) | 2020-06-26 | 2023-05-03 | The Procter & Gamble Company | Synergistic anti-inflammatory compositions |
| CN112225846B (zh) * | 2020-10-21 | 2021-11-09 | 广州市东雄化工有限公司 | 一种高屈服值、高透明度悬浮稳定剂和制备工艺及其应用 |
| JP7678101B2 (ja) | 2020-11-23 | 2025-05-15 | ザ プロクター アンド ギャンブル カンパニー | 硫酸化界面活性剤を含まないパーソナルケア組成物 |
| MX2023005963A (es) | 2020-12-04 | 2023-06-07 | Procter & Gamble | Composiciones para el cuidado del cabello que comprenden materiales de reduccion del mal olor. |
| US12409125B2 (en) | 2021-05-14 | 2025-09-09 | The Procter & Gamble Company | Shampoo compositions containing a sulfate-free surfactant system and sclerotium gum thickener |
| US11986543B2 (en) | 2021-06-01 | 2024-05-21 | The Procter & Gamble Company | Rinse-off compositions with a surfactant system that is substantially free of sulfate-based surfactants |
| US12458575B2 (en) | 2021-12-09 | 2025-11-04 | The Procter & Gamble Company | Sulfate free personal cleansing composition comprising effective preservation |
| CN115006374A (zh) * | 2022-07-13 | 2022-09-06 | 广州文翰生物科技有限公司 | 香兰基丁醚在制备治疗头屑和体癣产品中的应用 |
| WO2024019923A1 (en) * | 2022-07-20 | 2024-01-25 | Selora Haircare Llc | Hair treatment composition |
| WO2025194425A1 (en) * | 2024-03-21 | 2025-09-25 | L'oreal | Composition for cleansing and/or caring for keratin material |
| WO2025194426A1 (en) * | 2024-03-21 | 2025-09-25 | L'oreal | Composition for cleansing and/or caring for keratin material |
| CN118078729B (zh) * | 2024-04-23 | 2024-07-16 | 醇度国际生物科技(北京)有限公司 | 一种同时具有保湿和护肤作用的卸妆清洁霜及其制备方法 |
Family Cites Families (59)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2809971A (en) | 1955-11-22 | 1957-10-15 | Olin Mathieson | Heavy-metal derivatives of 1-hydroxy-2-pyridinethiones and method of preparing same |
| US3288770A (en) | 1962-12-14 | 1966-11-29 | Peninsular Chem Res Inc | Water soluble quaternary ammonium polymers |
| US3236733A (en) | 1963-09-05 | 1966-02-22 | Vanderbilt Co R T | Method of combatting dandruff with pyridinethiones metal salts detergent compositions |
| US3412019A (en) | 1965-05-25 | 1968-11-19 | Calgon Corp | Method of flocculating suspended particulate matter from an aqueous medium |
| US3541138A (en) | 1967-03-20 | 1970-11-17 | Rohm & Haas | Crosslinking polymerizable surfactants |
| US3761418A (en) | 1967-09-27 | 1973-09-25 | Procter & Gamble | Detergent compositions containing particle deposition enhancing agents |
| US4136163A (en) | 1971-02-04 | 1979-01-23 | Wilkinson Sword Limited | P-menthane carboxamides having a physiological cooling effect |
| US3753196A (en) | 1971-10-05 | 1973-08-14 | Kulite Semiconductor Products | Transducers employing integral protective coatings and supports |
| GB1421743A (en) | 1972-04-18 | 1976-01-21 | Wilkinson Sword Ltd | Ingestible topical and other compositions |
| DE3063434D1 (en) | 1979-05-16 | 1983-07-07 | Procter & Gamble Europ | Highly concentrated fatty acid containing liquid detergent compositions |
| US4384096A (en) | 1979-08-27 | 1983-05-17 | The Dow Chemical Company | Liquid emulsion polymers useful as pH responsive thickeners for aqueous systems |
| US4284532A (en) | 1979-10-11 | 1981-08-18 | The Procter & Gamble Company | Stable liquid detergent compositions |
| US4379753A (en) | 1980-02-07 | 1983-04-12 | The Procter & Gamble Company | Hair care compositions |
| US4345080A (en) | 1980-02-07 | 1982-08-17 | The Procter & Gamble Company | Pyridinethione salts and hair care compositions |
| US4323683A (en) | 1980-02-07 | 1982-04-06 | The Procter & Gamble Company | Process for making pyridinethione salts |
| US4470982A (en) | 1980-12-22 | 1984-09-11 | The Procter & Gamble Company | Shampoo compositions |
| US4421902A (en) | 1982-09-30 | 1983-12-20 | Rohm And Haas Company | Alkyl, poly(oxyethylene) poly(carbonyloxyethylene) acrylate emulsion copolymers for thickening purposes |
| USRE33156E (en) | 1984-08-23 | 1990-01-30 | Desoto, Inc. | Alkali soluble latex thickeners |
| US4514552A (en) | 1984-08-23 | 1985-04-30 | Desoto, Inc. | Alkali soluble latex thickeners |
| US4600761A (en) | 1985-04-04 | 1986-07-15 | Alco Chemical Corporation | Acrylic emulsion copolymers for thickening aqueous systems and copolymerizable surfactant monomers for use therein |
| US4686254A (en) | 1985-08-05 | 1987-08-11 | The B. F. Goodrich Company | Suspension composition for aqueous surfactant systems |
| US4616074A (en) | 1985-10-01 | 1986-10-07 | Alco Chemical Corporation | Acrylic-methylene succinic ester emulsion copolymers for thickening aqueous systems |
| US4772462A (en) | 1986-10-27 | 1988-09-20 | Calgon Corporation | Hair products containing dimethyl diallyl ammonium chloride/acrylic acid-type polymers |
| US5011978A (en) | 1989-03-02 | 1991-04-30 | National Starch And Chemical Investment Holding Corporation | Copolymers as thickeners and modifiers for latex systems |
| US5106609A (en) | 1990-05-01 | 1992-04-21 | The Procter & Gamble Company | Vehicle systems for use in cosmetic compositions |
| US5104646A (en) | 1989-08-07 | 1992-04-14 | The Procter & Gamble Company | Vehicle systems for use in cosmetic compositions |
| CA2050212C (en) | 1990-09-03 | 1997-09-30 | Andrew M. Murray | Hair treatment composition |
| CA2072175A1 (en) | 1991-06-28 | 1992-12-29 | Shih-Ruey T. Chen | Ampholyte terpolymers providing superior conditioning properties in shampoos and other hair care products |
| FR2684668B1 (fr) | 1991-12-04 | 1995-03-24 | Oreal | Composes hydro-fluoro-carbones, leur utilisation dans des compositions cosmetiques, leur procede de preparation et les compositions cosmetiques en comportant. |
| US5292843A (en) | 1992-05-29 | 1994-03-08 | Union Carbide Chemicals & Plastics Technology Corporation | Polymers containing macromonomers |
| IT1272109B (it) | 1993-03-19 | 1997-06-11 | Eniricerche Spa | Processo per la preparazione di apg |
| US5294692A (en) | 1993-06-30 | 1994-03-15 | National Starch And Chemical Investment Holding Corporation | Associative monomers and polymers |
| US5874495A (en) | 1994-10-03 | 1999-02-23 | Rhodia Inc. | Polymers useful as PH responsive thickeners and monomers therefor |
| US5770543A (en) | 1996-09-06 | 1998-06-23 | Henkel Corporation | Agricultural compositions comprising alkyl polyglycosides and fatty acids |
| US6200554B1 (en) | 1996-10-16 | 2001-03-13 | The Procter & Gamble Company | Conditioning shampoo compositions having improved silicone deposition |
| US6262152B1 (en) | 1998-10-06 | 2001-07-17 | E. I. Du Pont De Nemours And Company | Particles dispersed w/polymer dispersant having liquid soluble and cross-linkable insoluble segments |
| US6183766B1 (en) | 1999-02-12 | 2001-02-06 | The Procter & Gamble Company | Skin sanitizing compositions |
| DE60041699D1 (de) | 1999-06-25 | 2009-04-16 | Procter & Gamble | Topische antimikrobielle zusammensetzungen |
| US6635702B1 (en) | 2000-04-11 | 2003-10-21 | Noveon Ip Holdings Corp. | Stable aqueous surfactant compositions |
| US7001594B1 (en) | 2000-10-10 | 2006-02-21 | The Procter & Gamble Company | Scalp cosmetic compositions and corresponding methods of application to provide scalp moisturization and skin active benefits |
| US6573375B2 (en) | 2000-12-20 | 2003-06-03 | Union Carbide Chemicals & Plastics Technology Corporation | Liquid thickener for surfactant systems |
| GB0114197D0 (en) | 2001-06-11 | 2001-08-01 | Syngenta Ltd | Reactive polymeric surfactants |
| US8491877B2 (en) * | 2003-03-18 | 2013-07-23 | The Procter & Gamble Company | Composition comprising zinc-containing layered material with a high relative zinc lability |
| US20040213751A1 (en) | 2003-03-18 | 2004-10-28 | Schwartz James Robert | Augmentation of pyrithione activity or a polyvalent metal salt of pyrithione activity by zinc-containing layered material |
| ES2389776T3 (es) | 2005-05-31 | 2012-10-31 | Rhodia, Inc. | Composiciones que tienen modificadores reológicos HASE |
| ES2398125T3 (es) | 2006-03-30 | 2013-03-13 | Rhodia, Inc. | Tensioactivos reactivos y su uso en emulsiones y dispersiones |
| US7786027B2 (en) | 2006-05-05 | 2010-08-31 | The Procter & Gamble Company | Functionalized substrates comprising perfume microcapsules |
| EP2328547B1 (en) * | 2008-09-02 | 2014-03-05 | Basf Se | Copolymers useful as rheology modifiers and home and personal care compositions |
| ES2639444T3 (es) * | 2008-12-08 | 2017-10-26 | The Procter & Gamble Company | Composición para la higiene personal en forma de un artículo que tiene un recubrimiento hidrófobo que reside en la superficie |
| JP2011063564A (ja) * | 2009-09-18 | 2011-03-31 | Biochemical Laboratory Co Ltd | 育毛剤およびその製造方法 |
| BR112014004927A2 (pt) | 2011-08-29 | 2017-04-11 | Ethox Chemicals Llc | composto, látex polimérico, formulação de revestimento, composição de tensoativo reativo, formulação de revestimento curável por uv, dispersão de pigmento, e, pigmentos |
| JP6162121B2 (ja) * | 2011-09-13 | 2017-07-12 | ルブリゾル アドバンスド マテリアルズ， インコーポレイテッド | 界面活性剤応答性エマルジョン重合ミクロゲル |
| BR112014005923A2 (pt) * | 2011-09-13 | 2017-04-04 | Lubrizol Advanced Mat Inc | composição de fluido de limite de escoamento, fluido de perfuração para o uso na perfuração de formação subterrânea, fluido de fratura hidráulica para o uso na fratura de formações subterrâneas, e, uso de uma composição de fluido de limite de escoamento |
| EP2768904A4 (en) | 2011-10-21 | 2015-12-23 | Ethox Chemicals Llc | NEW REACTIVE SURFACES FOR FREEZER EMISSIONS EMULSION POLYMERS AND COATINGS MANUFACTURED THEREFROM |
| WO2013067109A1 (en) * | 2011-11-01 | 2013-05-10 | Lubrizol Advanced Materials, Inc. | Acrylate-olefin copolymers, methods for producing same and compositions utilizing same |
| US8574561B1 (en) | 2012-12-21 | 2013-11-05 | L'oreal | Compositions containing anti-dandruff agents |
| US9867768B2 (en) * | 2013-03-08 | 2018-01-16 | Lubrizol Advanced Materials, Inc. | Foaming performance in cleansing compositions through the use of nonionic, amphiphilic polymers |
| BR112016013854B1 (pt) * | 2013-12-17 | 2021-01-26 | Lubrizol Advanced Materials, Inc. | composições de polímero modificador de reologia anfifílico não iônico reticulado e fluida de tensão de deformação, e, fluidos de perfuração e de fratura hidráulico |
| US20160317424A1 (en) * | 2013-12-23 | 2016-11-03 | Lubrizol Advanced Materials, Inc. | Suspension and stability agent for antidandruff hair care compositions |
-
2015
- 2015-12-16 JP JP2017532811A patent/JP2017538732A/ja active Pending
- 2015-12-16 EP EP15817744.4A patent/EP3233026A1/en not_active Withdrawn
- 2015-12-16 US US15/536,885 patent/US20170367963A1/en not_active Abandoned
- 2015-12-16 KR KR1020177019928A patent/KR20170095373A/ko not_active Withdrawn
- 2015-12-16 CN CN201580076356.6A patent/CN107249558A/zh active Pending
- 2015-12-16 WO PCT/US2015/066021 patent/WO2016100466A1/en not_active Ceased
- 2015-12-16 BR BR112017012784A patent/BR112017012784A2/pt not_active Application Discontinuation
- 2015-12-17 AR ARP150104139A patent/AR103069A1/es unknown