JPH0460082B2 - - Google Patents
Info
- Publication number
- JPH0460082B2 JPH0460082B2 JP59055948A JP5594884A JPH0460082B2 JP H0460082 B2 JPH0460082 B2 JP H0460082B2 JP 59055948 A JP59055948 A JP 59055948A JP 5594884 A JP5594884 A JP 5594884A JP H0460082 B2 JPH0460082 B2 JP H0460082B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- formula
- polymer
- composition
- polymers
- 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.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 claims description 116
- 229920000642 polymer Polymers 0.000 claims description 64
- -1 -CH 2 - COOH Chemical group 0.000 claims description 50
- 125000004432 carbon atom Chemical group C* 0.000 claims description 47
- 125000000217 alkyl group Chemical group 0.000 claims description 45
- 229920006317 cationic polymer Polymers 0.000 claims description 33
- 229920001285 xanthan gum Polymers 0.000 claims description 26
- 229920006318 anionic polymer Polymers 0.000 claims description 24
- 229920001577 copolymer Polymers 0.000 claims description 22
- 239000000230 xanthan gum Substances 0.000 claims description 22
- 235000010493 xanthan gum Nutrition 0.000 claims description 22
- 229940082509 xanthan gum Drugs 0.000 claims description 22
- 125000002091 cationic group Chemical group 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 17
- 229920000768 polyamine Polymers 0.000 claims description 17
- 229920002907 Guar gum Polymers 0.000 claims description 16
- 239000000665 guar gum Substances 0.000 claims description 16
- 235000010417 guar gum Nutrition 0.000 claims description 16
- 229960002154 guar gum Drugs 0.000 claims description 16
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 15
- 229910052757 nitrogen Inorganic materials 0.000 claims description 14
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 13
- 239000000178 monomer Substances 0.000 claims description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
- 125000001931 aliphatic group Chemical group 0.000 claims description 11
- 125000002947 alkylene group Chemical group 0.000 claims description 11
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 11
- 150000007513 acids Chemical class 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 8
- 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 claims description 8
- 125000003277 amino group Chemical group 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 229910052708 sodium Inorganic materials 0.000 claims description 8
- 239000011734 sodium Substances 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 7
- 125000000129 anionic group Chemical group 0.000 claims description 7
- 239000003431 cross linking reagent Substances 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 239000006210 lotion Substances 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- 229920006395 saturated elastomer Polymers 0.000 claims description 7
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 238000004132 cross linking Methods 0.000 claims description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 229910052783 alkali metal Inorganic materials 0.000 claims description 5
- 239000000470 constituent Substances 0.000 claims description 5
- 229920001281 polyalkylene Polymers 0.000 claims description 5
- 238000006116 polymerization reaction Methods 0.000 claims description 5
- 229920001282 polysaccharide Polymers 0.000 claims description 5
- 239000005017 polysaccharide Substances 0.000 claims description 5
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 5
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 4
- 239000002280 amphoteric surfactant Substances 0.000 claims description 4
- 150000008064 anhydrides Chemical class 0.000 claims description 4
- 239000003945 anionic surfactant Substances 0.000 claims description 4
- 150000001450 anions Chemical class 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 229910052791 calcium Inorganic materials 0.000 claims description 4
- 239000011575 calcium Substances 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 4
- 239000002736 nonionic surfactant Substances 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 125000004193 piperazinyl group Chemical group 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 150000003335 secondary amines Chemical group 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 claims description 3
- GQWWGRUJOCIUKI-UHFFFAOYSA-N 2-[3-(2-methyl-1-oxopyrrolo[1,2-a]pyrazin-3-yl)propyl]guanidine Chemical group O=C1N(C)C(CCCN=C(N)N)=CN2C=CC=C21 GQWWGRUJOCIUKI-UHFFFAOYSA-N 0.000 claims description 3
- 239000004952 Polyamide Substances 0.000 claims description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
- 150000001242 acetic acid derivatives Chemical class 0.000 claims description 3
- 230000029936 alkylation Effects 0.000 claims description 3
- 238000005804 alkylation reaction Methods 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims description 3
- 239000003093 cationic surfactant Substances 0.000 claims description 3
- 229920002678 cellulose Polymers 0.000 claims description 3
- 239000001913 cellulose Substances 0.000 claims description 3
- 239000003086 colorant Substances 0.000 claims description 3
- 238000009833 condensation Methods 0.000 claims description 3
- 230000005494 condensation Effects 0.000 claims description 3
- 150000001991 dicarboxylic acids Chemical class 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 229920005610 lignin Polymers 0.000 claims description 3
- 229920002647 polyamide Polymers 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- 239000011591 potassium Substances 0.000 claims description 3
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- WDRZVZVXHZNSFG-UHFFFAOYSA-N 1-ethenylpyridin-1-ium Chemical group C=C[N+]1=CC=CC=C1 WDRZVZVXHZNSFG-UHFFFAOYSA-N 0.000 claims description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 2
- 229940100198 alkylating agent Drugs 0.000 claims description 2
- 239000002168 alkylating agent Substances 0.000 claims description 2
- 229920003086 cellulose ether Polymers 0.000 claims description 2
- 229920005565 cyclic polymer Polymers 0.000 claims description 2
- 239000003974 emollient agent Substances 0.000 claims description 2
- 150000002170 ethers Chemical class 0.000 claims description 2
- 239000003205 fragrance Substances 0.000 claims description 2
- 150000003893 lactate salts Chemical class 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 239000011777 magnesium Substances 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
- 230000003647 oxidation Effects 0.000 claims description 2
- 238000007254 oxidation reaction Methods 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 235000019161 pantothenic acid Nutrition 0.000 claims description 2
- 229920000172 poly(styrenesulfonic acid) Polymers 0.000 claims description 2
- 229940005642 polystyrene sulfonic acid Drugs 0.000 claims description 2
- 239000003755 preservative agent Substances 0.000 claims description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 2
- 238000005956 quaternization reaction Methods 0.000 claims description 2
- 239000003352 sequestering agent Substances 0.000 claims description 2
- LEDMRZGFZIAGGB-UHFFFAOYSA-L strontium carbonate Chemical class [Sr+2].[O-]C([O-])=O LEDMRZGFZIAGGB-UHFFFAOYSA-L 0.000 claims description 2
- 150000003460 sulfonic acids Chemical class 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 3
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims 2
- GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 claims 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims 1
- 229920002101 Chitin Polymers 0.000 claims 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 claims 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 claims 1
- 229910002651 NO3 Inorganic materials 0.000 claims 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims 1
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 claims 1
- 125000002723 alicyclic group Chemical group 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 150000001342 alkaline earth metals Chemical class 0.000 claims 1
- 125000002843 carboxylic acid group Chemical group 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 125000004427 diamine group Chemical group 0.000 claims 1
- AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical group C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 claims 1
- 229940050410 gluconate Drugs 0.000 claims 1
- 150000002500 ions Chemical class 0.000 claims 1
- 229940001447 lactate Drugs 0.000 claims 1
- 229910052744 lithium Inorganic materials 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 229940014662 pantothenate Drugs 0.000 claims 1
- 239000011713 pantothenic acid Substances 0.000 claims 1
- 238000006068 polycondensation reaction Methods 0.000 claims 1
- 229920005573 silicon-containing polymer Polymers 0.000 claims 1
- 125000001174 sulfone group Chemical group 0.000 claims 1
- 125000001302 tertiary amino group Chemical group 0.000 claims 1
- 239000002253 acid Substances 0.000 description 19
- 239000004480 active ingredient Substances 0.000 description 17
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical group [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 16
- 239000000047 product Substances 0.000 description 16
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 235000014113 dietary fatty acids Nutrition 0.000 description 11
- 239000000194 fatty acid Substances 0.000 description 11
- 229930195729 fatty acid Natural products 0.000 description 11
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000011780 sodium chloride Substances 0.000 description 8
- 159000000000 sodium salts Chemical class 0.000 description 8
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 7
- 239000001361 adipic acid Substances 0.000 description 7
- 235000011037 adipic acid Nutrition 0.000 description 7
- 239000002537 cosmetic Substances 0.000 description 7
- 229920001971 elastomer Polymers 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 239000002453 shampoo Substances 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 6
- 229920002472 Starch Polymers 0.000 description 6
- 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 6
- 229930006000 Sucrose Natural products 0.000 description 6
- 150000001412 amines Chemical group 0.000 description 6
- 230000003750 conditioning effect Effects 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 6
- 239000005720 sucrose Substances 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 5
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 5
- 241000282372 Panthera onca Species 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 230000014759 maintenance of location Effects 0.000 description 5
- 229920002401 polyacrylamide Polymers 0.000 description 5
- 239000002562 thickening agent Substances 0.000 description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
- 229920002554 vinyl polymer Polymers 0.000 description 5
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 4
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 4
- 244000215068 Acacia senegal Species 0.000 description 4
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 4
- 229920000084 Gum arabic Polymers 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 4
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 4
- 235000010489 acacia gum Nutrition 0.000 description 4
- 239000000205 acacia gum Substances 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- 150000004676 glycans Chemical class 0.000 description 4
- 229920001519 homopolymer Polymers 0.000 description 4
- 150000002430 hydrocarbons Chemical group 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000008107 starch Substances 0.000 description 4
- 235000019698 starch Nutrition 0.000 description 4
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 4
- 229920001567 vinyl ester resin Polymers 0.000 description 4
- 235000013162 Cocos nucifera Nutrition 0.000 description 3
- 244000060011 Cocos nucifera Species 0.000 description 3
- 244000303965 Cyamopsis psoralioides Species 0.000 description 3
- 229920001560 Cyanamer® Polymers 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 3
- 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 3
- 238000001035 drying Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003792 electrolyte Substances 0.000 description 3
- 238000000855 fermentation Methods 0.000 description 3
- 230000004151 fermentation Effects 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 125000005395 methacrylic acid group Chemical group 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 3
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 2
- PTHBKNSHSCMKBV-UHFFFAOYSA-N 4,6,8-trihydroxy-3-(2-hydroxyethyl)-2,3-dihydronaphtho[2,3-f][1]benzofuran-5,10-dione Chemical compound O=C1C2=CC(O)=CC(O)=C2C(=O)C2=C1C=C1OCC(CCO)C1=C2O PTHBKNSHSCMKBV-UHFFFAOYSA-N 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 150000003973 alkyl amines Chemical class 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 230000002152 alkylating effect Effects 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 150000001649 bromium compounds Chemical class 0.000 description 2
- 210000004534 cecum Anatomy 0.000 description 2
- 235000010980 cellulose Nutrition 0.000 description 2
- ALSTYHKOOCGGFT-UHFFFAOYSA-N cis-oleyl alcohol Natural products CCCCCCCCC=CCCCCCCCCO ALSTYHKOOCGGFT-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- TVFJAZCVMOXQRK-UHFFFAOYSA-N ethenyl 7,7-dimethyloctanoate Chemical compound CC(C)(C)CCCCCC(=O)OC=C TVFJAZCVMOXQRK-UHFFFAOYSA-N 0.000 description 2
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Classifications
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- 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
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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LU84708 | 1983-03-23 | ||
LU84708A LU84708A1 (fr) | 1983-03-23 | 1983-03-23 | Composition epaissie ou gelifiee de conditionnement des cheveux contenant au moins un polymere cationique,au moins un polymere anionique et au moins une gomme de xanthane |
Publications (2)
Publication Number | Publication Date |
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JPS59231008A JPS59231008A (ja) | 1984-12-25 |
JPH0460082B2 true JPH0460082B2 (US20040025266A1-20040212-C00001.png) | 1992-09-25 |
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JP59055948A Granted JPS59231008A (ja) | 1983-03-23 | 1984-03-23 | 毛髪調整用組成物 |
Country Status (14)
Families Citing this family (308)
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LU85549A1 (fr) * | 1984-09-21 | 1986-04-03 | Oreal | Compositions cosmetiques a base de silicone cationique et de gomme de xanthane |
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FR2580493B1 (fr) * | 1985-04-23 | 1988-06-10 | Oreal | Composition cosmetique de nettoyage, en particulier pour le demaquillage des yeux |
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LU86429A1 (fr) * | 1986-05-16 | 1987-12-16 | Oreal | Compositions cosmetiques renfermant un polymere cationique et un polymere anionique comme agent epaississant |
US4804705A (en) * | 1986-06-02 | 1989-02-14 | Franz Pum | Gel composition |
LU86547A1 (fr) * | 1986-08-07 | 1988-03-02 | Oreal | Suspension pour induire et stimuler la croissance des cheveux et diminuer leur chute a base de derives de la pyrimidine |
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LU86599A1 (fr) * | 1986-09-19 | 1988-04-05 | Oreal | Compositions cosmetiques a base de polymeres cationiques et de polymeres d'alkyloxazoline |
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DE4315405A1 (de) * | 1993-05-08 | 1994-11-10 | Wella Ag | Haarbehandlungsmittel |
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FR2788974B1 (fr) | 1999-01-29 | 2001-03-30 | Oreal | Composition anhydre de decoloration des fibres keratiniques comprenant l'association de polymeres amphiphiles anioniques et/ou non ioniques comportant au moins une chaine grasse et de polymeres substantifs cationiques ou amphoteres |
FR2788972B1 (fr) | 1999-02-03 | 2001-04-13 | Oreal | Composition capillaire comprenant une base lavante, un polymere cationique et un polyurethane anionique et utilisation |
FR2788973B1 (fr) | 1999-02-03 | 2002-04-05 | Oreal | Composition cosmetique comprenant un tensioactif anionique, un tensioactif amphotere, une huile de type polyolefine, un polymere cationique et un sel ou un alcool hydrosoluble, utilisation et procede |
FR2795310B1 (fr) | 1999-06-25 | 2003-02-14 | Oreal | Compositions cosmetiques contenant un polymere amphotere et un polymere fixant/conditionneur et leurs utilisations |
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FR2795635B1 (fr) | 1999-06-30 | 2006-09-15 | Oreal | Mascara comprenant des polymeres filmogenes |
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FR2799971B1 (fr) | 1999-10-20 | 2001-12-07 | Oreal | Compositions cosmetiques contenant un copolymere vinyldimethicone/dimethicone et un polymere cationique et leurs utilisations |
FR2802093B1 (fr) | 1999-12-08 | 2002-01-18 | Oreal | Composition pour la decoloration ou la deformation permanente des fibres keratiniques comprenant un polymere epaississant a squelette aminoplaste-ether |
FR2802092B1 (fr) | 1999-12-08 | 2002-01-18 | Oreal | Composition de decoloration pour fibres keratiniques comprenant un polymere epaississant a squelette aminoplaste-ether |
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FR2802094B1 (fr) | 1999-12-13 | 2002-01-18 | Oreal | Composition de decoloration pour fibres keratiniques comprenant une association de deux polyethers polyurethanes |
FR2803196B1 (fr) | 1999-12-30 | 2002-03-15 | Oreal | Composition pour la teinture d'oxydation des fibres keratiniques comprenant un alcool gras ayant plus de vingt atomes de carbone et un tensioactif non-ionique oxyalkylene de hlb superieure a 5 |
FR2803197B1 (fr) | 1999-12-30 | 2002-03-15 | Oreal | Composition pour la teinture d'oxydation des fibres keratiniques comprenant un polymere epaississant comportant au moins une chaine grasse et un alcool gras ayant plus de vingt atomes de carbone |
FR2803195B1 (fr) * | 1999-12-30 | 2002-03-15 | Oreal | Composition pour la teinture d'oxydation des fibres keratiniques comprenant un polymere epaississant comportant au moins une chaine grasse et un alcool gras mono-ou poly-glycerole |
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FR2813016B1 (fr) * | 2000-08-21 | 2002-10-11 | Oreal | Composition de decoloration des fibres keratiniques teintes |
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FR2816208B1 (fr) * | 2000-11-08 | 2003-01-03 | Oreal | Composition de teinture directe pour fibres keratiniques comprenant un polyurethane associatif cationique |
FR2816210B1 (fr) * | 2000-11-08 | 2005-02-25 | Oreal | Composition pour la decoloration ou la deformation permanente des fibres keratiniques comprenant un polyurethane associatif cationique |
FR2816207B1 (fr) * | 2000-11-08 | 2003-01-03 | Oreal | Composition de teinture d'oxydation pour fibres keratiniques comprenant un polyurethane associatif cationique |
FR2816209B1 (fr) * | 2000-11-08 | 2005-02-25 | Oreal | Composition de decoloration pour fibres keratiniques comprenant un polyurethane associatif cationique |
FR2816834B1 (fr) * | 2000-11-20 | 2005-06-24 | Oreal | Composition de traitement des fibres keratiniques comprenant un polymere polyurethane associatif cationique et un agent protecteur ou conditionneur |
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FR2817466B1 (fr) | 2000-12-04 | 2004-12-24 | Oreal | Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere associatif et un agent nacrant |
FR2819404B1 (fr) | 2001-01-12 | 2004-11-05 | Oreal | Compositions cosmetiques contenant un fructane et un polymere cationique et leurs utilisations |
FR2820031B1 (fr) * | 2001-01-26 | 2006-05-05 | Oreal | Composition cosmetique comprenant un polymere fixant et un poly(vinyllactame) cationique |
FR2820312B1 (fr) | 2001-02-02 | 2003-05-02 | Oreal | Composition pulverulente pour la decoloration des fibres keratiniques humaines |
FR2822683B1 (fr) * | 2001-03-30 | 2005-01-28 | Oreal | Compositions cosmetiques contenant un phosphate d'amidon et un polymere cationique et leurs utilisations |
FR2822680B1 (fr) * | 2001-03-30 | 2003-05-16 | Oreal | Compositions cosmetiques detergentes contenant un tensioactif anionique derive d'acides amines et un agent conditionneur soluble et leurs utilisations |
FR2824734B1 (fr) | 2001-05-16 | 2003-06-27 | Oreal | Composition pulverulente pour la decoloration des fibres keratiniques humaines |
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JPS4941277A (US20040025266A1-20040212-C00001.png) * | 1972-04-28 | 1974-04-18 | ||
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JPS57206606A (en) * | 1981-06-10 | 1982-12-18 | Hoou Kk | Solution for permanent wave |
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NL7104188A (en) * | 1971-03-29 | 1972-10-03 | Hair setting agent - contng hetero polysaccharide as active constituent | |
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- 1984-03-16 DK DK157984A patent/DK157984A/da not_active IP Right Cessation
- 1984-03-21 CA CA000450113A patent/CA1205749A/fr not_active Expired
- 1984-03-22 IT IT67276/84A patent/IT1178904B/it active
- 1984-03-22 CH CH1457/84A patent/CH659389A5/fr not_active IP Right Cessation
- 1984-03-22 GB GB08407477A patent/GB2136689B/en not_active Expired
- 1984-03-22 FR FR8404475A patent/FR2542997B1/fr not_active Expired
- 1984-03-22 ES ES530858A patent/ES8602393A1/es not_active Expired
- 1984-03-22 SE SE8401602A patent/SE8401602L/xx not_active Application Discontinuation
- 1984-03-23 NL NL8400929A patent/NL8400929A/nl not_active Application Discontinuation
- 1984-03-23 JP JP59055948A patent/JPS59231008A/ja active Granted
- 1984-03-23 US US06/592,934 patent/US4591610A/en not_active Expired - Lifetime
- 1984-03-23 DE DE19843410842 patent/DE3410842A1/de active Granted
- 1984-03-23 BE BE0/212624A patent/BE899237A/fr not_active IP Right Cessation
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US3658734A (en) * | 1970-10-20 | 1972-04-25 | Kelco Co | Guar gum-polyacrylamide compositions |
US3868340A (en) * | 1972-04-13 | 1975-02-25 | Warner Lambert Co | Denture adhesive preparation |
JPS4941277A (US20040025266A1-20040212-C00001.png) * | 1972-04-28 | 1974-04-18 | ||
JPS53139734A (en) * | 1977-03-15 | 1978-12-06 | Oreal | Keratin treating composition |
US4143007A (en) * | 1977-10-31 | 1979-03-06 | Celanese Corporation | Thickening agent containing a polygalactomannan gum and a copolymer of an olefinically unsaturated dicarboxylic acid anhydride useful in hydraulic well-treating |
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JPS57206606A (en) * | 1981-06-10 | 1982-12-18 | Hoou Kk | Solution for permanent wave |
Also Published As
Publication number | Publication date |
---|---|
ES530858A0 (es) | 1985-12-01 |
US4591610A (en) | 1986-05-27 |
DK157984A (da) | 1984-09-24 |
CA1205749A (fr) | 1986-06-10 |
IT1178904B (it) | 1987-09-16 |
DE3410842A1 (de) | 1984-09-27 |
SE8401602D0 (sv) | 1984-03-22 |
NL8400929A (nl) | 1984-10-16 |
FR2542997A1 (fr) | 1984-09-28 |
JPS59231008A (ja) | 1984-12-25 |
BE899237A (fr) | 1984-09-24 |
GB2136689B (en) | 1987-01-07 |
FR2542997B1 (fr) | 1987-10-23 |
ES8602393A1 (es) | 1985-12-01 |
DE3410842C2 (US20040025266A1-20040212-C00001.png) | 1991-01-03 |
GB2136689A (en) | 1984-09-26 |
IT8467276A1 (it) | 1985-09-22 |
IT8467276A0 (it) | 1984-03-22 |
CH659389A5 (fr) | 1987-01-30 |
SE8401602L (sv) | 1984-09-24 |
LU84708A1 (fr) | 1984-11-14 |
GB8407477D0 (en) | 1984-05-02 |
DK157984D0 (da) | 1984-03-16 |
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