BR102012032697A2 - composições e compostos de poliglicerila catiônica - Google Patents
composições e compostos de poliglicerila catiônica Download PDFInfo
- Publication number
- BR102012032697A2 BR102012032697A2 BR102012032697A BR102012032697A BR102012032697A2 BR 102012032697 A2 BR102012032697 A2 BR 102012032697A2 BR 102012032697 A BR102012032697 A BR 102012032697A BR 102012032697 A BR102012032697 A BR 102012032697A BR 102012032697 A2 BR102012032697 A2 BR 102012032697A2
- Authority
- BR
- Brazil
- Prior art keywords
- ammonium
- hydroxypropyl
- composition
- polyglyceryl
- cationic
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 287
- 125000002091 cationic group Chemical group 0.000 title claims abstract description 113
- 150000001875 compounds Chemical class 0.000 title claims abstract description 66
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 claims abstract description 44
- 238000012360 testing method Methods 0.000 claims abstract description 42
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 40
- 125000005647 linker group Chemical group 0.000 claims abstract description 27
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 24
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 11
- -1 2-hydroxypropyl Chemical group 0.000 claims description 118
- 125000000217 alkyl group Chemical group 0.000 claims description 62
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 50
- 229910052757 nitrogen Inorganic materials 0.000 claims description 50
- 239000000463 material Substances 0.000 claims description 41
- 238000000034 method Methods 0.000 claims description 22
- 125000001165 hydrophobic group Chemical group 0.000 claims description 20
- 230000000269 nucleophilic effect Effects 0.000 claims description 19
- 230000003750 conditioning effect Effects 0.000 claims description 15
- 239000003906 humectant Substances 0.000 claims description 15
- 125000002947 alkylene group Chemical group 0.000 claims description 11
- 125000000129 anionic group Chemical group 0.000 claims description 11
- 239000004094 surface-active agent Substances 0.000 claims description 11
- 238000006467 substitution reaction Methods 0.000 claims description 10
- 239000002904 solvent Substances 0.000 claims description 9
- 239000003974 emollient agent Substances 0.000 claims description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 239000003755 preservative agent Substances 0.000 claims description 6
- CMCBDXRRFKYBDG-UHFFFAOYSA-N 1-dodecoxydodecane Chemical compound CCCCCCCCCCCCOCCCCCCCCCCCC CMCBDXRRFKYBDG-UHFFFAOYSA-N 0.000 claims description 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 4
- 239000002738 chelating agent Substances 0.000 claims description 4
- 239000003205 fragrance Substances 0.000 claims description 4
- NPTLAYTZMHJJDP-KTKRTIGZSA-N [3-[3-[3-[3-[3-[3-[3-[3-[3-(2,3-dihydroxypropoxy)-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)CO NPTLAYTZMHJJDP-KTKRTIGZSA-N 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 239000003605 opacifier Substances 0.000 claims 1
- 239000011734 sodium Substances 0.000 description 76
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 47
- 229920006395 saturated elastomer Polymers 0.000 description 46
- 229910001868 water Inorganic materials 0.000 description 44
- 238000006243 chemical reaction Methods 0.000 description 43
- 230000000052 comparative effect Effects 0.000 description 43
- 150000001768 cations Chemical class 0.000 description 34
- 239000006260 foam Substances 0.000 description 32
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 31
- 229910052708 sodium Inorganic materials 0.000 description 31
- 244000060011 Cocos nucifera Species 0.000 description 30
- 235000013162 Cocos nucifera Nutrition 0.000 description 30
- 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 29
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 27
- 125000002252 acyl group Chemical group 0.000 description 27
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 26
- 229920000223 polyglycerol Polymers 0.000 description 26
- 239000000047 product Substances 0.000 description 26
- 239000003153 chemical reaction reagent Substances 0.000 description 25
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 21
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 20
- 239000002585 base Substances 0.000 description 20
- 239000000243 solution Substances 0.000 description 19
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 17
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 16
- 238000001179 sorption measurement Methods 0.000 description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- 125000000400 lauroyl group Chemical group O=C([*])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 description 15
- 238000009472 formulation Methods 0.000 description 14
- 239000000460 chlorine Substances 0.000 description 13
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- 239000012071 phase Substances 0.000 description 12
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- 229910052799 carbon Inorganic materials 0.000 description 10
- 229920001577 copolymer Polymers 0.000 description 10
- 150000002148 esters Chemical class 0.000 description 10
- 235000011187 glycerol Nutrition 0.000 description 10
- 229930182470 glycoside Natural products 0.000 description 10
- 241000894007 species Species 0.000 description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 230000008859 change Effects 0.000 description 9
- 238000004140 cleaning Methods 0.000 description 9
- 125000004122 cyclic group Chemical group 0.000 description 9
- 239000002736 nonionic surfactant Substances 0.000 description 9
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 8
- 239000006227 byproduct Substances 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 239000000194 fatty acid Substances 0.000 description 8
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 8
- 239000004593 Epoxy Substances 0.000 description 7
- 229910052783 alkali metal Inorganic materials 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 7
- 235000014113 dietary fatty acids Nutrition 0.000 description 7
- 229930195729 fatty acid Natural products 0.000 description 7
- 239000000499 gel Substances 0.000 description 7
- 230000001965 increasing effect Effects 0.000 description 7
- 150000003077 polyols Chemical class 0.000 description 7
- 210000001519 tissue Anatomy 0.000 description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 6
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 6
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 6
- 150000001340 alkali metals Chemical class 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 238000003795 desorption Methods 0.000 description 6
- 239000003085 diluting agent Substances 0.000 description 6
- 230000036541 health Effects 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 230000014759 maintenance of location Effects 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 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 description 6
- 238000009736 wetting Methods 0.000 description 6
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 5
- 208000027418 Wounds and injury Diseases 0.000 description 5
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 5
- 238000004364 calculation method Methods 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- 239000008103 glucose Substances 0.000 description 5
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 5
- 150000004820 halides Chemical class 0.000 description 5
- 150000003944 halohydrins Chemical class 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000002609 medium Substances 0.000 description 5
- 125000001421 myristyl 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])[H] 0.000 description 5
- 150000007524 organic acids Chemical class 0.000 description 5
- 125000005429 oxyalkyl group Chemical group 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 150000003512 tertiary amines Chemical group 0.000 description 5
- 238000004448 titration Methods 0.000 description 5
- OEBXWWBYZJNKRK-UHFFFAOYSA-N 1-methyl-2,3,4,6,7,8-hexahydropyrimido[1,2-a]pyrimidine Chemical compound C1CCN=C2N(C)CCCN21 OEBXWWBYZJNKRK-UHFFFAOYSA-N 0.000 description 4
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 235000010469 Glycine max Nutrition 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 4
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 150000003863 ammonium salts Chemical class 0.000 description 4
- 239000002280 amphoteric surfactant Substances 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
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- GHVNFZFCNZKVNT-UHFFFAOYSA-M decanoate Chemical compound CCCCCCCCCC([O-])=O GHVNFZFCNZKVNT-UHFFFAOYSA-M 0.000 description 4
- 125000002704 decyl 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])* 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
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- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
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- WQPMYSHJKXVTME-UHFFFAOYSA-N 3-hydroxypropane-1-sulfonic acid Chemical compound OCCCS(O)(=O)=O WQPMYSHJKXVTME-UHFFFAOYSA-N 0.000 description 3
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- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
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- LWZFANDGMFTDAV-BURFUSLBSA-N [(2r)-2-[(2r,3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O LWZFANDGMFTDAV-BURFUSLBSA-N 0.000 description 3
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- 229920001983 poloxamer Polymers 0.000 description 1
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- 229920000768 polyamine Polymers 0.000 description 1
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- 229940099549 polyglycerin-3 Drugs 0.000 description 1
- 229940061570 polyglyceryl-10 stearate Drugs 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229940068977 polysorbate 20 Drugs 0.000 description 1
- 229940068965 polysorbates Drugs 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- PYJBVGYZXWPIKK-UHFFFAOYSA-M potassium;tetradecanoate Chemical compound [K+].CCCCCCCCCCCCCC([O-])=O PYJBVGYZXWPIKK-UHFFFAOYSA-M 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- GMVPRGQOIOIIMI-DWKJAMRDSA-N prostaglandin E1 Chemical compound CCCCC[C@H](O)\C=C\[C@H]1[C@H](O)CC(=O)[C@@H]1CCCCCCC(O)=O GMVPRGQOIOIIMI-DWKJAMRDSA-N 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- SBYHFKPVCBCYGV-UHFFFAOYSA-N quinuclidine Chemical compound C1CC2CCN1CC2 SBYHFKPVCBCYGV-UHFFFAOYSA-N 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 230000037390 scarring Effects 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 230000036299 sexual function Effects 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
- 230000037075 skin appearance Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 229940080230 sodium c12-14 olefin sulfonate Drugs 0.000 description 1
- 229940031688 sodium c14-16 olefin sulfonate Drugs 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 description 1
- 229940045998 sodium isethionate Drugs 0.000 description 1
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- 229940075560 sodium lauryl sulfoacetate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 229940048107 sodium methyl 2-sulfolaurate Drugs 0.000 description 1
- SLBXZQMMERXQAL-UHFFFAOYSA-M sodium;1-dodecoxy-4-hydroxy-1,4-dioxobutane-2-sulfonate Chemical compound [Na+].CCCCCCCCCCCCOC(=O)C(S(O)(=O)=O)CC([O-])=O SLBXZQMMERXQAL-UHFFFAOYSA-M 0.000 description 1
- UAJTZZNRJCKXJN-UHFFFAOYSA-M sodium;2-dodecoxy-2-oxoethanesulfonate Chemical compound [Na+].CCCCCCCCCCCCOC(=O)CS([O-])(=O)=O UAJTZZNRJCKXJN-UHFFFAOYSA-M 0.000 description 1
- LADXKQRVAFSPTR-UHFFFAOYSA-M sodium;2-hydroxyethanesulfonate Chemical compound [Na+].OCCS([O-])(=O)=O LADXKQRVAFSPTR-UHFFFAOYSA-M 0.000 description 1
- CSKVLUWCGPWCQR-UHFFFAOYSA-M sodium;3-hydroxypropane-1-sulfonate Chemical compound [Na+].OCCCS([O-])(=O)=O CSKVLUWCGPWCQR-UHFFFAOYSA-M 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- UUCCCPNEFXQJEL-UHFFFAOYSA-L strontium dihydroxide Chemical compound [OH-].[OH-].[Sr+2] UUCCCPNEFXQJEL-UHFFFAOYSA-L 0.000 description 1
- 229910001866 strontium hydroxide Inorganic materials 0.000 description 1
- 150000003445 sucroses Chemical class 0.000 description 1
- AGGIJOLULBJGTQ-UHFFFAOYSA-N sulfoacetic acid Chemical class OC(=O)CS(O)(=O)=O AGGIJOLULBJGTQ-UHFFFAOYSA-N 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical class S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 238000004441 surface measurement Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 229940061605 tetrasodium glutamate diacetate Drugs 0.000 description 1
- UZVUJVFQFNHRSY-OUTKXMMCSA-J tetrasodium;(2s)-2-[bis(carboxylatomethyl)amino]pentanedioate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CC[C@@H](C([O-])=O)N(CC([O-])=O)CC([O-])=O UZVUJVFQFNHRSY-OUTKXMMCSA-J 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
- PUVAFTRIIUSGLK-UHFFFAOYSA-M trimethyl(oxiran-2-ylmethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1CO1 PUVAFTRIIUSGLK-UHFFFAOYSA-M 0.000 description 1
- YFHICDDUDORKJB-UHFFFAOYSA-N trimethylene carbonate Chemical compound O=C1OCCCO1 YFHICDDUDORKJB-UHFFFAOYSA-N 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 230000005186 women's health Effects 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
- LTVDFSLWFKLJDQ-UHFFFAOYSA-N α-tocopherolquinone Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)(O)CCC1=C(C)C(=O)C(C)=C(C)C1=O LTVDFSLWFKLJDQ-UHFFFAOYSA-N 0.000 description 1
Classifications
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- A61K8/442—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
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- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C217/28—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having one amino group and at least two singly-bound oxygen atoms, with at least one being part of an etherified hydroxy group, bound to the carbon skeleton, e.g. ethers of polyhydroxy amines
- C07C217/40—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having one amino group and at least two singly-bound oxygen atoms, with at least one being part of an etherified hydroxy group, bound to the carbon skeleton, e.g. ethers of polyhydroxy amines having at least two singly-bound oxygen atoms, with at least one being part of an etherified hydroxy group, bound to the same carbon atom of the carbon skeleton, e.g. amino-ketals, ortho esters
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/10—1,4-Dioxanes; Hydrogenated 1,4-dioxanes
- C07D319/12—1,4-Dioxanes; Hydrogenated 1,4-dioxanes not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
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- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/30—Characterized by the absence of a particular group of ingredients
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
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- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Chemical & Material Sciences (AREA)
- Dermatology (AREA)
- Organic Chemistry (AREA)
- Emergency Medicine (AREA)
- Dispersion Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
- Polyethers (AREA)
- Detergent Compositions (AREA)
Abstract
Description
Claims (20)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US13/331,157 US8986665B2 (en) | 2007-06-29 | 2011-12-20 | Cationic polyglyceryl compositions and compounds |
US13/331.157 | 2011-12-20 |
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BR102012032697A2 true BR102012032697A2 (pt) | 2015-12-08 |
BR102012032697B1 BR102012032697B1 (pt) | 2018-12-04 |
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BR102012032697-3A BR102012032697B1 (pt) | 2011-12-20 | 2012-12-20 | composições de poliglicerila para cuidados pessoais e método de umedecimento ou condicionamento da pele ou do cabelo |
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US (4) | US8986665B2 (pt) |
EP (1) | EP2695598B1 (pt) |
KR (1) | KR102011640B1 (pt) |
CN (1) | CN103172609B (pt) |
AU (1) | AU2012261564B2 (pt) |
BR (1) | BR102012032697B1 (pt) |
CA (1) | CA2798996C (pt) |
CO (1) | CO6980141A1 (pt) |
MX (1) | MX362199B (pt) |
RU (1) | RU2012155466A (pt) |
SA (1) | SA112340100B1 (pt) |
ZA (1) | ZA201209653B (pt) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9469725B2 (en) | 2012-06-28 | 2016-10-18 | Johnson & Johnson Consumer Inc. | Ultraviolet radiation absorbing polymers |
US9255180B2 (en) | 2012-06-28 | 2016-02-09 | Johnson & Johnson Consumer Inc. | Ultraviolet radiation absorbing polyethers |
AU2013280569B2 (en) | 2012-06-28 | 2017-11-16 | Johnson & Johnson Consumer Inc. | Sunscreen compositions containing an ultraviolet radiation-absorbing polymer |
US10874603B2 (en) | 2014-05-12 | 2020-12-29 | Johnson & Johnson Consumer Inc. | Sunscreen compositions containing a UV-absorbing polyglycerol and a non-UV-absorbing polyglycerol |
WO2016077327A1 (en) | 2014-11-10 | 2016-05-19 | The Procter & Gamble Company | Personal care compositions with two benefit phases |
US10966916B2 (en) | 2014-11-10 | 2021-04-06 | The Procter And Gamble Company | Personal care compositions |
MX2017006148A (es) | 2014-11-10 | 2017-07-27 | Procter & Gamble | Composiciones para el cuidado personal con dos fases beneficas. |
FR3043782B1 (fr) * | 2015-11-13 | 2017-12-08 | Horiba Abx Sas | Dispositif d'agitation et de prelevement d'echantillons de liquides biologiques adapte pour trier |
EP3246384A1 (de) * | 2016-05-18 | 2017-11-22 | Basf Se | Wässrige tensid-zusammensetzungen |
US10596087B2 (en) | 2016-10-05 | 2020-03-24 | Johnson & Johnson Consumer Inc. | Ultraviolet radiation absorbing polymer composition |
CN111212625B (zh) | 2017-10-20 | 2023-05-23 | 宝洁公司 | 气溶胶泡沫洁肤剂 |
WO2019079405A1 (en) | 2017-10-20 | 2019-04-25 | The Procter & Gamble Company | AEROSOL FOAMING CLEANSER FOR THE SKIN |
WO2020112486A1 (en) | 2018-11-29 | 2020-06-04 | The Procter & Gamble Company | Methods for screening personal care products |
CN111214843B (zh) * | 2020-03-02 | 2022-04-26 | 黄冈永安日用化工有限公司 | 一种高品质甲基牛磺酸钠的蒸馏装置及生产方法 |
US20210338541A1 (en) | 2020-04-22 | 2021-11-04 | Johnson & Johnson Consumer Inc. | Method of using in situ complexation of surfactants for foam control and conditioning |
FR3110573B1 (fr) * | 2020-05-20 | 2024-01-19 | Exsymol Sa | Compositions comprenant des composés organo-silanols, et applications. |
Family Cites Families (48)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3654261A (en) | 1968-06-27 | 1972-04-04 | Cpc International Inc | Quaternary ammonium alkoxide alkoxy polyol compounds |
US3931148A (en) | 1974-12-23 | 1976-01-06 | Basf Wyandotte Corporation | Hydroxyalkylamino glycosides and process of preparation |
US4292212A (en) | 1978-11-29 | 1981-09-29 | Henkel Corporation | Shampoo creme rinse |
US4205063A (en) | 1979-04-12 | 1980-05-27 | Johnson Products Co., Inc. | Low irritant conditioning shampoo composition |
US4512856A (en) * | 1979-11-19 | 1985-04-23 | Enthone, Incorporated | Zinc plating solutions and method utilizing ethoxylated/propoxylated polyhydric alcohols |
US4263178A (en) * | 1979-11-26 | 1981-04-21 | The Gillette Company | Hair shampoo composition |
US4803071A (en) | 1980-02-11 | 1989-02-07 | National Starch And Chemical Corporation | Hair care compositions |
US4689217A (en) | 1983-10-07 | 1987-08-25 | Ici Americas Inc. | Amine and ammonium nitrogen containing polyvinyl alcohol polymers having improved lipophilic properties for use in skin conditioning, cosmetic and pharmaceutical formulations |
US4676978A (en) | 1983-10-17 | 1987-06-30 | Colgate-Palmolive Company | Shampoo |
ES2061668T3 (es) | 1987-09-17 | 1994-12-16 | Procter & Gamble | Barra de tocador para limpieza de la piel con bajo contenido de humedad. |
US4987526A (en) | 1989-02-02 | 1991-01-22 | Massachusetts Institute Of Technology | System to provide high speed, high accuracy motion |
US5138043A (en) | 1989-12-07 | 1992-08-11 | Union Carbide Chemicals & Plastics Technology Corporation | Alkoxylated alkyl glucoside ether quaternaries useful in personal care |
GB9021417D0 (en) | 1990-10-02 | 1990-11-14 | Unilever Plc | Cosmetic composition |
BR9107153A (pt) * | 1990-12-05 | 1993-11-16 | Procter & Gamble | Composicoes de xampu com silicone e agentes de condicionamento tensoativos cationicos |
US5648348A (en) | 1991-10-28 | 1997-07-15 | Mona Industries, Inc. | Phospholipid antimicrobial compositions |
US5286719A (en) | 1991-10-28 | 1994-02-15 | Mona Industries, Inc. | Phospholipid virucidal compositions |
US5215976A (en) | 1991-10-28 | 1993-06-01 | Mona Industries, Inc. | Phospholipids useful as spermicidal agents |
US5288484A (en) | 1992-05-15 | 1994-02-22 | Anne Tashjian | Cationic cellulose derivative containing fatty quaternum groups in a pre-shampoo conditioning composition |
FI94135C (fi) | 1993-12-27 | 1995-07-25 | Raisio Chem Oy | Kationisen tärkkelyksen valmistusmenetelmä |
US5482704A (en) | 1994-06-28 | 1996-01-09 | National Starch And Chemical Investment Holding Corporation | Cosmetic compositions containing amino-multicarboxylate modified starch |
JP3458256B2 (ja) * | 1995-07-21 | 2003-10-20 | ライオン株式会社 | 毛髪洗浄剤組成物 |
EP0758641B1 (en) | 1995-08-11 | 2000-08-30 | Daicel Chemical Industries, Ltd. | A fatty acid esters composition of a polyglycerine, a process for the preparation thereof, a process for the preparation of a highly-purified fatty acid esters composition of a polyglycerine, a highly-purified fatty acid esters composition of a polyglycerine, an additive for food-stuffs, a resin composition, and a composition for cosmetics or detergents |
DE69712884T2 (de) | 1996-03-14 | 2002-11-21 | Johnson & Johnson Consumer | Reinigende und feuchthaltende tensidzusammensetzungen |
DE19818410A1 (de) | 1998-04-24 | 1999-10-28 | Wella Ag | Haar- und Körperreinigungsmittel mit verminderter Hautirritation |
US6642198B2 (en) | 1998-12-16 | 2003-11-04 | Johnson & Johnson Consumer Companies, Inc. | Clear cleansing detergent systems |
CA2382081C (en) | 1999-12-03 | 2010-01-05 | Calgon Corporation | Modified starch solutions and their use in personal care |
CN1194975C (zh) | 2003-03-31 | 2005-03-30 | 湖南化工研究院 | 一种具有生物活性的杂环取代苯并噁嗪环类化合物 |
FI20030769A0 (fi) | 2003-05-21 | 2003-05-21 | Raisio Chem Oy | Tärkkelysjohdannaiset, niiden valmistus ja käyttö |
US7759296B2 (en) | 2003-06-19 | 2010-07-20 | Lubrizol Advanced Materials, Inc. | Cationic polymers and fixative application therefor |
FR2865401B1 (fr) | 2004-01-27 | 2006-04-28 | Oreal | Composition de nettoyage de la peau |
JP4405832B2 (ja) | 2004-03-15 | 2010-01-27 | 中央化学株式会社 | フラックス組成物 |
DE102004034915A1 (de) | 2004-07-14 | 2006-04-06 | Beiersdorf Ag | Reinigungsgel |
US7507399B1 (en) | 2004-08-05 | 2009-03-24 | Surfatech Corporation | Functionalized polymeric surfactants based upon alkyl polyglycosides |
KR101082601B1 (ko) | 2004-08-10 | 2011-11-10 | 주식회사 엘지생활건강 | 산화 영구 염모제 조성물 |
US7087560B2 (en) | 2004-10-25 | 2006-08-08 | Unilever Home & Personal Care Usa, A Division Of Conopco, Inc. | Personal care composition with salts of dihydroxypropyltri(C1-C3 alkyl) ammonium monosubstituted polyols |
US7282471B2 (en) | 2005-09-08 | 2007-10-16 | Conopco, Inc. | Personal care compositions with glycerin and hydroxypropyl quaternary ammonium salts |
DE102004054035A1 (de) | 2004-11-05 | 2006-05-11 | Cognis Ip Management Gmbh | Mischungen von quaternären und nichtionischen Tensiden |
EP1661547A1 (en) | 2004-11-24 | 2006-05-31 | KAO CHEMICALS GmbH | Foam-enhancing agent containing polyglycerol |
EP2079762B1 (en) | 2005-12-08 | 2012-10-03 | Chemigate Oy | A process for the preparation of hydroxy polymer esters and their use |
KR20070082219A (ko) | 2006-02-15 | 2007-08-21 | 주식회사 엘지생활건강 | 혼합 계면활성제 시스템 |
US7659234B2 (en) | 2006-03-07 | 2010-02-09 | Conopco, Inc. | Personal care compositions containing quaternary ammonium trihydroxy substituted dipropyl ether |
JP2007269730A (ja) * | 2006-03-31 | 2007-10-18 | Kao Corp | (ポリ)グリセリルエーテルの製造方法 |
US7335627B1 (en) | 2006-05-25 | 2008-02-26 | Surfa Tech Corporation | Polymeric alkylpolyglycoside carboxylates |
US7803403B2 (en) | 2006-11-09 | 2010-09-28 | Johnson & Johnson Consumer Companies, Inc. | Low-irritation compositions and methods of making the same |
US7375064B1 (en) | 2007-02-20 | 2008-05-20 | Surfatech Corporation | Functionalized polymeric surfactants based upon alkyl polyglycosides |
GB0709460D0 (en) * | 2007-05-17 | 2007-06-27 | Croda Int Plc | Method of making polyglycerol esters |
GB0714817D0 (en) * | 2007-07-31 | 2007-09-12 | Croda Int Plc | Polyglycerol derivatives |
JP5296521B2 (ja) * | 2008-12-26 | 2013-09-25 | 花王株式会社 | ヘアトリートメント組成物 |
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US20150104402A1 (en) | 2015-04-16 |
MX362199B (es) | 2019-01-08 |
US20150104401A1 (en) | 2015-04-16 |
ZA201209653B (en) | 2014-12-23 |
US8986665B2 (en) | 2015-03-24 |
BR102012032697B1 (pt) | 2018-12-04 |
AU2012261564A1 (en) | 2013-07-04 |
MX2013000202A (es) | 2013-06-19 |
EP2695598A2 (en) | 2014-02-12 |
SA112340100B1 (ar) | 2015-07-07 |
CO6980141A1 (es) | 2014-06-27 |
KR20130071403A (ko) | 2013-06-28 |
KR102011640B1 (ko) | 2019-08-19 |
CA2798996A1 (en) | 2013-06-20 |
CN103172609B (zh) | 2016-06-08 |
EP2695598A3 (en) | 2015-04-22 |
US10285923B2 (en) | 2019-05-14 |
AU2012261564B2 (en) | 2014-11-20 |
EP2695598B1 (en) | 2017-09-13 |
CN103172609A (zh) | 2013-06-26 |
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