MXPA97008330A - Polioxylycylene compounds in heteric blocks, liquid, which have better fluidity characteristics - Google Patents
Polioxylycylene compounds in heteric blocks, liquid, which have better fluidity characteristicsInfo
- Publication number
- MXPA97008330A MXPA97008330A MXPA/A/1997/008330A MX9708330A MXPA97008330A MX PA97008330 A MXPA97008330 A MX PA97008330A MX 9708330 A MX9708330 A MX 9708330A MX PA97008330 A MXPA97008330 A MX PA97008330A
- Authority
- MX
- Mexico
- Prior art keywords
- integer
- oxide
- ethylene oxide
- limited
- initiator
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 30
- 239000007788 liquid Substances 0.000 title claims abstract description 29
- 239000000203 mixture Substances 0.000 claims description 93
- GOOHAUXETOMSMM-UHFFFAOYSA-N propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 47
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 38
- 125000002947 alkylene group Chemical group 0.000 claims description 37
- IAYPIBMASNFSPL-UHFFFAOYSA-N oxane Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 35
- 239000003999 initiator Substances 0.000 claims description 31
- 229920001223 polyethylene glycol Polymers 0.000 claims description 16
- -1 but not limited to Substances 0.000 claims description 14
- 239000004094 surface-active agent Substances 0.000 claims description 14
- 229920001400 block copolymer Polymers 0.000 claims description 12
- MHAJPDPJQMAIIY-UHFFFAOYSA-N hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 12
- 229910052783 alkali metal Chemical group 0.000 claims description 11
- 150000001340 alkali metals Chemical group 0.000 claims description 11
- 229910052784 alkaline earth metal Chemical group 0.000 claims description 11
- 150000001342 alkaline earth metals Chemical group 0.000 claims description 11
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 11
- 125000001424 substituent group Chemical group 0.000 claims description 11
- UIIMBOGNXHQVGW-UHFFFAOYSA-M NaHCO3 Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 10
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 239000000551 dentifrice Substances 0.000 claims description 9
- 239000002202 Polyethylene glycol Substances 0.000 claims description 8
- 239000003906 humectant Substances 0.000 claims description 8
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 6
- 235000011187 glycerol Nutrition 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 5
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 5
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 4
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 4
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 claims description 4
- 239000000600 sorbitol Substances 0.000 claims description 4
- 241000416162 Astragalus gummifer Species 0.000 claims description 3
- 229960003563 Calcium Carbonate Drugs 0.000 claims description 3
- 229940043256 Calcium Pyrophosphate Drugs 0.000 claims description 3
- JUNWLZAGQLJVLR-UHFFFAOYSA-J Calcium pyrophosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])(=O)OP([O-])([O-])=O JUNWLZAGQLJVLR-UHFFFAOYSA-J 0.000 claims description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 claims description 3
- 241000003823 Soleirolia soleirolii Species 0.000 claims description 3
- 229920001615 Tragacanth Polymers 0.000 claims description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 3
- 235000010216 calcium carbonate Nutrition 0.000 claims description 3
- 235000019821 dicalcium diphosphate Nutrition 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 3
- 229960001407 sodium bicarbonate Drugs 0.000 claims description 3
- 235000019333 sodium laurylsulphate Nutrition 0.000 claims description 3
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 claims description 3
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2R,3R,4S,5R,6S)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2S,3R,4S,5R,6R)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2R,3R,4S,5R,6R)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 claims description 2
- OXLXSOPFNVKUMU-UHFFFAOYSA-N 1,4-dioctoxy-1,4-dioxobutane-2-sulfonic acid Chemical compound CCCCCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCCCCC OXLXSOPFNVKUMU-UHFFFAOYSA-N 0.000 claims description 2
- NEFBYIFKOOEVPA-UHFFFAOYSA-K Dicalcium phosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])([O-])=O NEFBYIFKOOEVPA-UHFFFAOYSA-K 0.000 claims description 2
- 235000019739 Dicalciumphosphate Nutrition 0.000 claims description 2
- 229920000569 Gum karaya Polymers 0.000 claims description 2
- 229940039371 Karaya Gum Drugs 0.000 claims description 2
- 229940005550 Sodium alginate Drugs 0.000 claims description 2
- BFDWBSRJQZPEEB-UHFFFAOYSA-L Sodium monofluorophosphate Chemical compound [Na+].[Na+].[O-]P([O-])(F)=O BFDWBSRJQZPEEB-UHFFFAOYSA-L 0.000 claims description 2
- 229960002799 Stannous Fluoride Drugs 0.000 claims description 2
- 241000934878 Sterculia Species 0.000 claims description 2
- ANOBYBYXJXCGBS-UHFFFAOYSA-L Tin(II) fluoride Chemical compound F[Sn]F ANOBYBYXJXCGBS-UHFFFAOYSA-L 0.000 claims description 2
- 229940116362 Tragacanth Drugs 0.000 claims description 2
- 238000005296 abrasive Methods 0.000 claims description 2
- 239000011230 binding agent Substances 0.000 claims description 2
- 239000001506 calcium phosphate Substances 0.000 claims description 2
- 229940038472 dicalcium phosphate Drugs 0.000 claims description 2
- 229910000390 dicalcium phosphate Inorganic materials 0.000 claims description 2
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 claims description 2
- 239000012025 fluorinating agent Substances 0.000 claims description 2
- 235000010494 karaya gum Nutrition 0.000 claims description 2
- 239000000231 karaya gum Substances 0.000 claims description 2
- 229920000609 methyl cellulose Polymers 0.000 claims description 2
- 239000001923 methylcellulose Substances 0.000 claims description 2
- MSXHSNHNTORCAW-UHFFFAOYSA-M sodium 3,4,5,6-tetrahydroxyoxane-2-carboxylate Chemical compound [Na+].OC1OC(C([O-])=O)C(O)C(O)C1O MSXHSNHNTORCAW-UHFFFAOYSA-M 0.000 claims description 2
- 235000010413 sodium alginate Nutrition 0.000 claims description 2
- 239000000661 sodium alginate Substances 0.000 claims description 2
- 239000011775 sodium fluoride Substances 0.000 claims description 2
- 235000013024 sodium fluoride Nutrition 0.000 claims description 2
- 229960000414 sodium fluoride Drugs 0.000 claims description 2
- 229960004711 sodium monofluorophosphate Drugs 0.000 claims description 2
- ADWNFGORSPBALY-UHFFFAOYSA-M sodium;2-[dodecyl(methyl)amino]acetate Chemical compound [Na+].CCCCCCCCCCCCN(C)CC([O-])=O ADWNFGORSPBALY-UHFFFAOYSA-M 0.000 claims description 2
- 235000010487 tragacanth Nutrition 0.000 claims description 2
- 239000000196 tragacanth Substances 0.000 claims description 2
- 239000007787 solid Substances 0.000 description 17
- 239000000463 material Substances 0.000 description 15
- 229920001577 copolymer Polymers 0.000 description 11
- 239000000796 flavoring agent Substances 0.000 description 11
- 229920000642 polymer Polymers 0.000 description 11
- 235000019634 flavors Nutrition 0.000 description 10
- 239000000606 toothpaste Substances 0.000 description 10
- 229940034610 Toothpaste Drugs 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 9
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- 238000009472 formulation Methods 0.000 description 8
- 229920001983 poloxamer Polymers 0.000 description 8
- 239000000499 gel Substances 0.000 description 7
- 239000000969 carrier Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000002537 cosmetic Substances 0.000 description 6
- 239000002736 nonionic surfactant Substances 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 229920002023 Pluronic® F 87 Polymers 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- 229920001451 Polypropylene glycol Polymers 0.000 description 4
- 235000019658 bitter taste Nutrition 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 239000003974 emollient agent Substances 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000002324 mouth wash Substances 0.000 description 3
- 229920001992 poloxamer 407 Polymers 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- HVYWMOMLDIMFJA-DPAQBDIFSA-N (3β)-Cholest-5-en-3-ol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- POJWUDADGALRAB-PVQJCKRUSA-N Allantoin Natural products NC(=O)N[C@@H]1NC(=O)NC1=O POJWUDADGALRAB-PVQJCKRUSA-N 0.000 description 2
- HUCVOHYBFXVBRW-UHFFFAOYSA-M Caesium hydroxide Chemical compound [OH-].[Cs+] HUCVOHYBFXVBRW-UHFFFAOYSA-M 0.000 description 2
- 229940051866 Mouthwash Drugs 0.000 description 2
- 239000004264 Petrolatum Substances 0.000 description 2
- 229940066842 Petrolatum Drugs 0.000 description 2
- 229940068918 Polyethylene Glycol 400 Drugs 0.000 description 2
- MWNQXXOSWHCCOZ-UHFFFAOYSA-M Sodium percarbonate Chemical compound [Na+].OOC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-M 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 230000001166 anti-perspirant Effects 0.000 description 2
- 239000003213 antiperspirant Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 235000003599 food sweetener Nutrition 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 239000003349 gelling agent Substances 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229940045872 sodium percarbonate Drugs 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000003765 sweetening agent Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000003039 volatile agent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- GPLRAVKSCUXZTP-UHFFFAOYSA-N 3-(2,3-dihydroxypropoxy)propane-1,2-diol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- CWSZBVAUYPTXTG-UHFFFAOYSA-N 5-[6-[[3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxymethyl]-3,4-dihydroxy-5-[4-hydroxy-3-(2-hydroxyethoxy)-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)-2-methyloxane-3,4-diol Chemical compound O1C(CO)C(OC)C(O)C(O)C1OCC1C(OC2C(C(O)C(OC)C(CO)O2)OCCO)C(O)C(O)C(OC2C(OC(C)C(O)C2O)CO)O1 CWSZBVAUYPTXTG-UHFFFAOYSA-N 0.000 description 1
- 229940116904 ANTIINFLAMMATORY THERAPEUTIC RADIOPHARMACEUTICALS Drugs 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 229960000458 Allantoin Drugs 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K Aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229940113118 Carrageenan Drugs 0.000 description 1
- 229960004830 Cetylpyridinium Drugs 0.000 description 1
- 229960001927 Cetylpyridinium Chloride Drugs 0.000 description 1
- YMKDRGPMQRFJGP-UHFFFAOYSA-M Cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 1
- 229940107161 Cholesterol Drugs 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N Dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N Dodecanol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 229940039717 Lanolin Drugs 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- ZADPBFCGQRWHPN-UHFFFAOYSA-N OBO Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 description 1
- 229940074726 OPHTHALMOLOGIC ANTIINFLAMMATORY AGENTS Drugs 0.000 description 1
- 240000007817 Olea europaea Species 0.000 description 1
- 229920002565 Polyethylene Glycol 400 Polymers 0.000 description 1
- FKHIFSZMMVMEQY-UHFFFAOYSA-N Talc Chemical compound [Mg+2].[O-][Si]([O-])=O FKHIFSZMMVMEQY-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N Triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- DVBBEGGVSYJLME-UHFFFAOYSA-N aluminum;hydrochloride Chemical compound [Al].Cl DVBBEGGVSYJLME-UHFFFAOYSA-N 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000000844 anti-bacterial Effects 0.000 description 1
- 239000002260 anti-inflammatory agent Substances 0.000 description 1
- 230000002882 anti-plaque Effects 0.000 description 1
- 239000008365 aqueous carrier Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 239000000337 buffer salt Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000004075 cariostatic agent Substances 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- NEUSVAOJNUQRTM-UHFFFAOYSA-N cetylpyridinium Chemical compound CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 NEUSVAOJNUQRTM-UHFFFAOYSA-N 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000008278 cosmetic cream Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000004673 fluoride salts Chemical class 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- TVZISJTYELEYPI-UHFFFAOYSA-N hypodiphosphoric acid Chemical compound OP(O)(=O)P(O)(O)=O TVZISJTYELEYPI-UHFFFAOYSA-N 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 230000000873 masking Effects 0.000 description 1
- 239000001525 mentha piperita l. herb oil Substances 0.000 description 1
- 239000001683 mentha spicata herb oil Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 235000019477 peppermint oil Nutrition 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002335 preservative Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000001681 protective Effects 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- VQOIVBPFDDLTSX-UHFFFAOYSA-M sodium;3-dodecylbenzenesulfonate Chemical class [Na+].CCCCCCCCCCCCC1=CC=CC(S([O-])(=O)=O)=C1 VQOIVBPFDDLTSX-UHFFFAOYSA-M 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 235000019605 sweet taste sensations Nutrition 0.000 description 1
- 235000019640 taste Nutrition 0.000 description 1
- 230000000699 topical Effects 0.000 description 1
- 238000005429 turbidity Methods 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Abstract
The present invention relates to liquid polyoxyalkylene compounds that have improved flow characteristics useful in a variety of industrial and personal care applications.
Description
POLIOXYLYCYLENE COMPOUNDS IN HETERIC BLOCKS, LIQUIDS, WHICH HAVE IMPROVED FLUIDITY CHARACTERISTICS
FIELD OF THE INVENTION The present invention relates to liquid, heterogeneous block polyoxyalkylene compounds, which are homogeneous and have improved flow characteristics.
BACKGROUND Polyoxyalkylene block copolymers are well known to those skilled in the art of nonionic surfactants. Specifically, U.S. Patent 3,740,421 (Schmolka) assigned to BASF discloses aqueous gels that are prepared using a polyoxyethylene / polyoxypropylene block copolymer suitable for pharmaceutical and personal care compositions. U.S. Patent 3,639,574 (Schamolka) assigned to BASF discloses polyoxyethylene / polyoxypropylene block copolymers as gelling agents for hydrogen peroxide compositions. U.S. Patent 4,465,663, (Schmolka) assigned to BASF discloses polyoxybutylene / polyoxypropylene block copolymers as gelling agents for aqueous gels useful in pharmaceutical and personal care applications. Some of these compounds are sold by BASF Corporation under the trade name of
PLURONIC®. Additionally, US Patents 4,272,394 and 4,411,810 disclose the use of polyoxyalkylene block polymers in applications for tackle washing machines. U.S. Patent 4,925,988 describes the use of a nonionic surfactant in a specific combination of alkanol, ethylene oxide and propylene oxide useful for automatic dishwashing application. U.S. Patent 5,374,368 describes the use of the copolymers in three EO / PO / EO liquid blocks (PLURONIC® L 31 and L 35 surfactants) in stable dental care compositions that release hydrogen peroxide in concentrations of 55-90% by weight of the composition for dental care. US Pat. No. 3,740,421 describes the three-block EO / PO / EO copolymers, solids, gel formers, useful in cosmetic formulations and for personal care in concentrations of approximately 20-25% by weight. Preferred solid, EO / PO / EO three-block copolymers have a molecular weight of 4,600-16,000. These copolymers in three EO / PO / EO blocks, solid, form a gel when they are added to an aqueous solution. U.S. Patent 3,867,533 discloses aqueous gel compositions containing copolymers in three EO / PO / EO blocks, solids, with a molecular weight of 6.450-20,000, useful in concentrations of about 20% by weight. These compositions are
useful for preparing cosmetic formulations. U.S. Patent 4,465,663 discloses aqueous cosmetic gels containing copolymers in three blocks of EO / BO (butylene oxide) / EO, solids in concentrations of about 20%. U.S. Patent 5,035,880 discloses dentifrice compositions, stable containing a cetylpyridinium bactericide and the three block copolymers, EO / PO / EO solids, (PLURONIC® F 127 surfactant) and polyethylene glycol in concentrations of 15-80% by weight, US Patent 4,476,107 discloses a mouthwash containing copolymers in three blocks EO / BO (butylene oxide) / EO in concentrations of 0.5-5.0% by weight. U.S. Patent 5,057,307 describes oral hygiene gels containing nonionic surfactants, coating substances and viscosity modifiers. These nonionic surfactants are PLURONIC® F 108 and F 127 surfactants available from BASF Corporation, Mt. Olive, New Jersey. U.S. Patent 5,256,396 describes a topical composition containing an EO / PO / EO three-block copolymer, solid
(PLURONIC® F 127 surfactant) used at a concentration of more than 10% to about 17% by weight. Patent EPO-546-627A describes compositions for mouthwash containing copolymers in three blocks, solids, of EO / PO / EO as surfactants PLURONIC® L 108, F 88, in concentrations
of 0.5-3% by weight. U.S. Patent 5,073,368 describes mouthwashes containing copolymers in three blocks of EO / PO / EO, solids, as surfactant PLURONIC® F 87 in concentrations of 0.1-3% by weight. WO 93/13750 discloses an eye cleaning composition containing copolymers in three blocks, PLURONIC® F87 solid and in PLURONIC® P 85 paste. The PLURONIC® P 85 surfactant is 4-9% by weight of the cleaning composition, the PLURONIC® F 87 surfactant is 0.5-2% by weight of the cleaning composition. Finally, US Pat. No. 5,096,698 discloses a toothpaste composition containing a three-block EO / PO / EO, liquid, non-ionic copolymer, or an EO / PO / EO, three-block copolymer, solid, in concentrations of 0.1-5. % by weight. These copolymers help to avoid phase separation. The surfactant PLURONIC® F 108 (solid) is more preferred, followed by the surfactants PLURONIC® F 87, PLURONIC® F 127 and PLURONIC® L 72. US Pat. No. 4,272,394 describes the nonionic surfactant, with low foaming power, novel, for compositions for machine washing machines. U.S. Patent 4,411,810 discloses a nonionic surfactant, with low foaming power, low cloud point, in compositions for washing machines. U.S. Patents 5,496,452, 5,374,368 and 5,424,060 describe
the use of a polyoxyalkylene compound to prepare a stable percarbonate formulation, as well as a dentifrice composition. U.S. Patent 5,187,191 discloses polyoxyalkylene ester block surfactants in formulations for agricultural use. Finally, Japanese Patent JP47-48366 B4 describes a process for producing liquid, tasteless, heteroteryl polyoxyalkylene compounds of molecular weight 1000 or higher. However, a major problem with these polymeric materials is that they have high pour points (closer to ambient temperatures) which limits their use in processes of cosmetic compositions and toiletries. In addition, the polymers of Japanese Patent Application 47-48366 B4 develop a higher degree of crystallinity which manifests as turbidity and solids precipitated during storage. Applicants have surprisingly discovered a method for producing polyoxyalkylene compounds in heteric, liquid blocks, with pour point significantly lower (i.e., closer to solidification temperatures) which substantially increases their utility in personal care compositions. In addition, the inventive polymers of the applicants were neutralized with common inorganic acids resulting essentially in compositions
transparent and almost free of solids precipitated during storage. The applicants have achieved this by selectively controlling the distribution or placement of propylene oxide and ethylene oxide in the inventive polymers of the applicants. If limited to the theory, the applicants wish to emphasize that it is of particular importance to control the distribution or placement of the alkylene oxides of C3 or higher in the polymer chain, to effectively reduce or eliminate the formation of crystalline segments in the polymer. . When crystalline segments are allowed to form in the polymers, the crystalline segments are separated from the solution causing a two-phase, unwanted product. The applicants' approach to overcoming this problem in the art differs from the method described in Japanese Patent Application 47-48366 B4 wherein the alkylene oxides are randomly distributed throughout the polymer chain. These polymers, as described in Japanese Patent 47-48366 B4 which consist solely of a random distribution of the alkylene oxides throughout the polymer chain are outside the scope of the applicants' invention.Definitions and terms HOMOGENEITY is a term used to
characterize the single phase, the physical form of the polyoxyalkylene compound in the heteric block of this invention. FLUIDITY refers to the ease of spillage of the liquid polyoxyalkylene compounds of this invention. The ease of spillage is manifested in the values of the spill points shown by the compounds in heteric, liquid blocks. HETERIC BLOCK The liquid polyoxyalkylene polymer of the present invention is a block copolymer of which at least one block is composed of a mixture of ethylene oxide and C3-e alkylene oxides randomized. This random arrangement of ethylene oxide and the alkylene oxides of C3-e is known as a heteric block.
The present invention relates to a polyoxyalkylene compound in heteric block, liquid, with better characteristics of flow and homogeneity, which tends the formula: I- [(AO) a- [(EO) b (XO) c] - ( EO) dM] x; wherein: I is an initiator or a mixture of initiators having at least one substituent selected from the group including, but not limited to OH, NH2 or COOH;
AO is an alkylene oxide of 2-6 carbons or a mixture of alkylene oxides of 2-6 carbons arranged randomly or in a block sequence; EO is ethylene oxide; XO is a portion of alkylene oxide having 3-6 carbon atoms; M is hydrogen or alkali metal or alkaline earth metal; a is an integer from about 1-20; b is an integer from about 5-1500; c is an integer from about 2-700; d is an integer from about 1-15; x is an integer from about 1-8; The present invention furthermore relates to a method of making a liquid, heteric block polyoxyalkylene compound having improved flow characteristics, which has the formula: I- [(AO) a- [(EO) b (XO)] c] - (EO) dM] x; wherein I is an initiator or a mixture of initiators having at least one substituent selected from the group including, but not limited to OH, NH2 or COOH; AO is an alkylene oxide of 2-6 carbons or a mixture of alkylene oxides of 2-6 carbons arranged randomly or in a block sequence: EO is ethylene oxide and XO is a portion of ethylene oxide having 3-6 carbon atoms;
M is a hydrogen or an alkali metal or alkaline earth metal; a is an integer from about 1-20; b is an integer from about 5-1500; c is an integer from about 2-700; d is an integer from about 1-15; x is an integer from about 1-8; which comprises the steps of: adding AO to an initiator and catalyst followed by b adding a mixture of EO and XO followed by, c adding EO. The molecular weight range is around 1,000-100,000.
DETAILED DESCRIPTION The present invention relates to a polyoxyalkylene compound in heteric block, liquid, with better characteristics of fluidity and homogeneity, tending the formula: I- [(AO) a- [(EO) b (XO) c] - (EO) dM] x; wherein: I is an initiator or a mixture of initiators having at least one substituent selected from the group including, but not limited to OH, NH2 or COOH; AO is an alkylene oxide of 2-6 carbons or a mixture of alkylene oxides of 2-6 carbons arranged randomly or in
a sequence of blocks; EO is ethylene oxide; XO is a portion of alkylene oxide having 3-6 carbon atoms; M is hydrogen or alkali metal or alkaline earth metal; a is an integer from about 1-20; b is an integer from about 5-1500; c is an integer from about 2-700; d is an integer from about 1-15; x is an integer from about 1-8; The present invention furthermore relates to a method of making a liquid, heteric block polyoxyalkylene compound having improved flow characteristics, which has the formula: I- [(AO) a- [(EO) b (XO)] c] - (EO) dM] x; wherein I is an initiator or a mixture of initiators having at least one substituent selected from the group including, but not limited to OH, NH2 or COOH; AO is an alkylene oxide of 2-6 carbons or a mixture of alkylene oxides of 2-6 carbons arranged randomly or in a block sequence: EO is ethylene oxide and XO is a portion of ethylene oxide having 3-6 carbon atoms; M is a hydrogen or an alkali metal or alkaline earth metal; a is an integer from about 1-20;
b is an integer from about 5-1500; c is an integer from about 2-700; d is an integer from about 1-15; x is an integer from about 1-8; which comprises the steps of: adding AO to an initiator and catalyst followed by b adding a mixture of EO and XO followed by, c adding EO. The molecular weight range is around 1,000-100,000. Preferably, the initiator is selected from propylene glycol (PG), dipropylene glycol, ethylene glycol, triethylene glycol and glycerol, most preferably, the initiator is propylene glycol (PG). This initiator has at least one substituent selected from the group that includes, but is not limited to OH, NH 2 or COOH. AO is a portion of an alkylene oxide having 2-6 carbons, preferably the alkylene oxide portion is ethylene oxide, propylene oxide or butylene oxide, more preferably ethylene oxide, propylene oxide or ethylene oxide and propylene oxide, more preferably ethylene oxide or ethylene oxide and propylene oxide. In addition, AO can be a mixture of alkylene oxides with 2-6 carbons arranged randomly or in block sequences.
XO is a portion of alkylene oxide having from 3-6 carbons, preferably, this portion of alkylene oxide and is propylene oxide or butylene oxide, more preferably, propylene oxide. M is H or a catalyst selected from the group including, but not limited to alkali metal or alkaline earth metal bases, lithium hydroxide, potassium hydroxide, cesium hydroxide and most preferably potassium hydroxide. a preferably is about 1-20, more preferably about 1-10, most preferably 2-8. b is preferably about 5-1500, more preferably about 5-500, most preferably about 7-16. c is preferably about 1-700, more preferably about 1-250, most preferably about 1-10. d is preferably about 1-15, more preferably about 1-10, most preferably about 1-5 x is preferably about 1-8, most preferably about 2-3, most preferably about 2 The molecular weight range is almost 1,000-100,000. The most preferred values for molecular weight are from about 1,000-25,000.
The most preferred molecular weight is from about 1,000-3,000.
DESCRIPTION OF THE METHOD OF MANUFACTURE OF POLYMEXALKYLENE IN HETERIC BLOCK, LIQUID OF THE PRESENT INVENTION Note: The charges of ethylene oxide and oxides mixed in these experiments were added with nitrogen at 34 psig with addition rates to maintain the EO concentration in the vapor phase. below the explosive safety limit which can be calculated according to Siwek in Siwek R.,
Rozenberg, E., "Ethylene Oxide Vapor Decomposition-Process and Protective Measures" Zeitschrift fur die fett-, 01-, Tensid-, Kosmetik- undPharmaindutrie, Vol. 115, Augsburg, September 1, 1989, NR14-1. A two gallon stainless steel autoclave was charged with 1089 g of propylene glycol, 46.6 g of 45% potassium hydroxide and purged with nitrogen. The contents were heated to 80 ° C and distilled to remove the volatiles for 2.5 hours. The contents were heated to 130 ° C and the pressure in the vessel was adjusted to 34 psig with nitrogen. The ethylene oxide (4412.9 g) was added over a period of 6 hours. After the addition was completed the mixture was maintained at 130 ° C for 1 hour and then the volatiles were removed for half an hour. A five-gallon stainless steel autoclave will
charged with 3075.6 g of the aforementioned material and purged with nitrogen. The material was heated to 116 ° C and 11.168 g of a mixture of ethylene oxide at 76.8% by weight and propylene oxide at 23.2% by weight were added over a period of 9.5 hours. After the addition was completed, the mixture was maintained at 116 ° C for an additional 2 hours. A final charge of 1762 g of ethylene oxide was added for 2 hours and then maintained at 116 ° C for 2 hours. The mixture was distilled for half an hour, it was cooled to 80 ° C and 30.1 g of 50% hypophosphoric acid or 17.5 g of 85% phosphoric acid were added. The mixture was stirred for half an hour in the autoclave and then discharged. alternatively, the material can be treated with magnesium silicate and filtered instead of neutralized with acid. Table 1 Comparison of the present invention with polyethylene glycol 400 and heteric materials. Material PEG PEG ABCBEFGH 400 2000 20% 20% 20% 23% 23% 25% 25% 25% PO PO PO PO PO PO weight 400 2000 2000 2000 2000 2000 2000 2000 2000 2000 2000 molecular point of 5.0 52.0 13 9 4.4 3.3 -0.5 6.1 -3.9 -5.0 fluency ° C amount nin solid +++ +++ +++ ++ ++ ++ <; + + of gun sediment * or @ 21 ° C flavor very flavor flavor flavor flavor flavor flavor flavor flavor flavor smooth r r r r r r r io mellow mellow mellow mellow mellow mellow mellow mellow mellow
* ++++ sediment most + minimum sediment, little solid present PEG 400 is a polyethylene glycol of molecular weight 400. PEG 2000 is a polyethylene glycol of molecular weight 2000. The percentage of propylene oxide (PO) is calculated as the percentage of the total weight that contributes to the initiator of propylene glycol (PG) and propylene oxide. Sample A is a comparative sample of an all-heteric material similar to that of JP 478366 B4
Sample B of the present invention has the structure:
PG [(E03.5 (E012.2 \ P02.8) (EO) 2.5H] 2 The sample C of the present invention has the structure: PG [(EO PO EOe.?POi.β) (EO) 4H] 2 The sample D of the present invention has the structure: PG [(EO) 3.5 (EO) ??.? PO 3.3 (EO) 2.5H] 2 Sample E of the present invention has the structure:
PG [(E06 (PO)? 7 (E07.5 \ PO 1.7) (EO) 4 H] 2 Sample F is a comparative sample of an all-heteric material similar to that of JP 478366 B4 PG - [(E017 \ P03.7) H] 2 Sample G of the present invention has the structure:
Sample H of the present invention has the structure:
PG [(EO) 6 (PO)? 9E07 \ PO ig) (EO) 4H] 2 The material of all heteric with 20% PO compared to materials in heteric blocks with 20% PO prepared in accordance with this invention (B and C) show that A has a considerably high pour point. Materials with PO at 25%, F, G and H show the same behavior. Examples D and E are given as further evidence of the tendency of lower pour points when materials are made according to this invention. The amount of sedimented material in these samples is also considerably lower for those that are made incorporating heteric blocks according to this invention. The pour point comparison of Polyethylene glycol 400 with examples C, D, E, G and H of the present invention show a pour point reduction despite the fact that the molecular weights of these materials are higher. The pour point for the PEG 2000 is 52 ° C. Utility of Polyoxyalkylene Compounds Having Improved Flowability Because the polyoxyalkylene compounds made according to the method of the present invention have improved flow characteristics, they are useful in
a variety of pharmaceutical and personal care applications, particularly as carriers for personal care compositions.
Personal care The compounds prepared according to the method of the present invention are particularly useful in personal care, particulate compositions in oral care compositions, such as toothpastes. Toothpaste formulations usually contain substantial amounts of humectants. The humectants help the formulation maintain its moisture, thus preventing the formation of hardening when the lid of the container is left open for prolonged periods. The common moisturizers that are used in these formulations are glycerol, sorbitol which are usually the preferred humectants due to their sweet taste. Other humectants that are also used are polyethylene glycols of molecular weight usually between 200-600. For economic reasons, a combination of humectants is used in most formulations for personal care. At present toothpaste compositions are being formulated without significant water incorporation. The examples of these toothpaste compositions are those that do not tolerate
presence of significant levels of water due to the aspects related to the decomposition of the key ingredients that give rise to the loss of activity or the reactivity of the ingredients, for example, sodium bicarbonate and a peroxygen composition such as hydrogen peroxide or percarbonate of sodium. The formulation and increased stability of these toothpaste compositions is achieved by employing a non-aqueous carrier that is usually selected from liquid polyethylene glycols of low molecular weight. Toothpaste compositions containing peroxygen source and sodium bicarbonate are usually formulated by premixing toothpaste ingredients in the presence of a liquid protractor, as liquid polyethylene glycol to achieve a composition with consistency similar to toothpaste. The choice of liquid polyethylene glycols as carriers for non-aqueous formulations has several advantages, such as good hygroscopicity, low viscosity, good compatibility with various dentifrice ingredients, low volatility, low cost, low toxicity, low odor and low pour point. However, a significant disadvantage that is associated with the use of low molecular weight polyethylene glycols is their bitter taste. The bitter taste of liquid polyethylene glycols gives the finished formulation an unpleasant taste that often has to be marketed
by including expensive sweeteners or masking agents. A large number of pharmaceutical compositions which are orally administered, and furthermore limited to use the liquid polyethylene glycols as carriers at present have little flexibility to modify the bitter taste of the resulting composition. The polyalkylene glycols in heteric, liquid blocks of the present invention, which are essentially transparent and almost free of precipitates, and have no bitter taste, can serve as suitable carriers for various compositions for personal care, oral care and pharmaceuticals that fall within the scope of the invention. in contact with the human body.
Preparation of Personal Care Compositions Containing the Novel Polyoxyalkylene Compound of the Present Invention The liquid, heteric block polyoxyalkylene compounds of the present invention are presented in personal care compositions at preferred concentrations of 1-99%, more preference at a concentration of 20-79%; more preferably at a concentration of 30-50% by weight of the composition for personal care. In general, the level of incorporation depends on the final use of the liquid polyoxyalkylene compound of the invention. Yes
they function as carriers, for example, in an essentially non-aqueous dentifrice formulation, then higher use levels in the formulation are necessary. The personal care formulations may also contain other ingredients such as surfactants that are selected from anionic surfactants including sodium lauryl sulfate; sodium alkyl glyceryl ether sulfonate; alkyl benzene sulfonates. Other anionic surfactants also include oxyalkylates of Ce-C? & It is also known to those skilled in the art to use block copolymers, solids, polyoxyethylene and polyoxypropylene to further provide a reinforcement in the foaming function of the dentifrice composition. In addition, small amounts of cationic surfactants having quaternary nitrogen can also be used, which shows compatibility with the nonionic carrier mixtures of this invention. It is also possible to use various other materials in the formulation of personal care products. For example, peroxygen compounds such as hydrogen peroxide, sodium percarbonate can be used in these dentifrice compositions. In a toothpaste, dental abrasives consisting of finely divided silica or calcium carbonate, sodium bicarbonate, calcium pyrophosphate and hydrated alumina are added to function as
polishers. Additionally, thickeners such as xanthan gum, gum arabic, hydroxyethylcellulose, polyvinylpyrrolidone, gum tragacanth, carrageenan can also be used to provide sufficient thickening consistency to the formulation. Also, flavoring agents such as peppermint oils, spearmint oils, or preservatives, opacifying agents, buffer salts, sweeteners, antibacterial agents or antiplaque agents, anti-inflammatory agents, anticaries agents such as fluoride salts may also be included in small amounts. Polymeric agents that accelerate the transport of active materials can also be included. Also, emollients of cosmetic creams such as glycerin, mineral oil and petrolatum can be added. The personal care products are formulated according to methods known to those skilled in the art. Representative formulations of personal care products are described in Cosmetics, Science Technology, 2nd Edition, Vol.l, Edited by M-S. Balsam, et al., And A Formulary of Cosmetic Preparations, Michael and Iren Ash, Chemical Publishing, N-Y., N-Y., And both are incorporated herein by reference. The following non-limiting examples will furthermore serve to illustrate the utility of the present invention. Everybody
the percentages are in percent by weight of the total composition unless otherwise indicated.
Tooth composition: 1-55% abrasive which is selected from the group including, but not limited to, anhydrous dicalcium phosphate, calcium carbonate, calcium pyrophosphate and sodium bicarbonate. 0-0.6% of a fluorinating agent that includes, but is not limited to, stannous fluoride, sodium fluoride, sodium monofluorophosphate. 2-10% binders including, but not limited to, karaya gum, USP tragacanth, sodium alginate, Irish moss and methylcellulose. 0-10% of a peroxygen source that includes, but is not limited to, hydrogen peroxide, sodium percarbonate. 0-8% surfactants including, but not limited to sodium lauryl sulfate, sodium N-lauryl sarcosinate; sodium dioctyl sulfosuccinate. 0-5% block copolymers of EO and PO. 5-50% humectants including, but not limited to glycerin, propylene glycol; sorbitol; polyethylene glycol. 5-70% polyoxyalkylene compound that has the
formula: I- [(AO) a- [(EO) b (XO) c] - (EO) d-M] x; wherein: I is an initiator or a mixture of initiators having at least one substituent selected from the group including, but not limited to OH, NH2 or COOH; AO is an alkylene oxide of 2-6 carbons or a mixture of alkylene oxides of 2-6 carbons arranged randomly or in a block sequence; EO is ethylene oxide; XO is a portion of alkylene oxide having 3-6 carbon atoms; M is hydrogen or alkali metal or alkaline earth metal; a is an integer from about 1-20; b is an integer from about 5-1500; c is an integer from about 2-700; d is an integer from about 1-15; x is an integer from about 1-8;
Composition for body cleansing: 1-5% emollients that include, but are not limited to lanolin, sterols (cholesterol) and fatty acids. 0.1-3% barrier forming agents that include but are not limited to petrolatum, beeswax, casein. 0.01-0.1% healing agents that include, but are not limited to
to allantoin and urea. 2-20% humectants including, but not limited to, glycerin; polyethylene glycol; sorbitol; polyethylene glycol. 0.01-1% thickeners that include, but are not limited to guar gum, cellulose derivatives and Irish moss. 0.5-3% emulsifiers including, but not limited to, cetylpyridinium chloride; polyoxyethylene lauryl alcohol. 5-70% polyoxyalkylene compound having the formula: I- [(AO) a- [(EO) b (XO) c] - (EO) d-M] x; wherein: I is an initiator or a mixture of initiators having at least one substituent selected from the group including, but not limited to OH, NH2 or COOH; AO is an alkylene oxide of 2-6 carbons or a mixture of alkylene oxides of 2-6 carbons arranged randomly or in a block sequence; EO is ethylene oxide; XO is a portion of alkylene oxide having 3-6 carbon atoms; M is hydrogen or alkali metal or alkaline earth metal; a is an integer from about 1-20; b is an integer from about 5-1500;
c is an integer from about 2-700; d is an integer from about 1-15; x is an integer from about 1-8;
Antiperspirant deodorant composition: 36-50% aluminum hydrochloride or 1-15% zinc oxide or 1-15% boronic acid 5-70% polyoxyalkylene compound: I- [(AO) a- [(EO) b (XO) c] - (EO) dM] x; wherein: I is an initiator or a mixture of initiators having at least one substituent selected from the group including, but not limited to OH, NH2 or COOH; AO is an alkylene oxide of 2-6 carbons or a mixture of alkylene oxides of 2-6 carbons arranged randomly or in a block sequence; EO is ethylene oxide; XO is a portion of alkylene oxide having 3-6 carbon atoms; M is hydrogen or alkali metal or alkaline earth metal; a is an integer from about 1-20; b is an integer from about 5-1500; c is an integer from about 2-700; d is an integer from about 1-15;
x is an integer from about 1-8; 25-50% SD alcohol (40)
The antiperspirant compositions may also contain emollients and perfume.
Claims (3)
-
- A polyoxyalkylene compound in heteric block, liquid, with characteristics of improved fluidity and homogeneity, which tends the formula: I- [(AO) a- [(EO) b (XO) d- (EO) d-M] x; wherein: I is an initiator or a mixture of initiators having at least one substituent selected from the group including, but not limited to OH, NH2 or COOH; AO is an alkylene oxide of 2-6 carbons or a mixture of alkylene oxides of 2-6 carbons arranged randomly or in a block sequence; EO is ethylene oxide; XO is a portion of alkylene oxide that has
- 3-6 carbon atoms; M is hydrogen or alkali metal or alkaline earth metal; a is an integer from about 1-20; b is an integer from about 5-1500; c is an integer from about 2-700; d is an integer from about 1-15; x is an integer from about 1-8; The polyoxyalkylene compound in heteric block, liquid, of claim 1, wherein the initiator I is propylene glycol, AO is ethylene oxide or ethylene oxide and propylene oxide, XO is propylene oxide, M is H, a is 1-10, b is 5- 500, c is 1-250, d is 1-10 and x is 2. The polyoxyalkylene compound in the liquid, heteric block of claim 1, wherein the initiator I is propylene glycol, AO is ethylene oxide or ethylene oxide and propylene oxide, XO is propylene oxide, M is H, a is 2-8, b is 7-16, c is 1-10, d is 1 -5 and x is 2. A method of making a polyoxyalkylene compound in heteric blocks, liquid, having improved characteristics of fluidity and homogeneity, having the formula: I- [(AO) a- [(EO) b (XO) c] - (EO) dM] x; wherein I is an initiator or a mixture of initiators having at least one substituent selected from the group including, but not limited to OH, NH2 or COOH; AO is an alkylene oxide of 2-6 carbons or a mixture of alkylene oxides of 2-6 carbons arranged randomly or in a block sequence; EO is ethylene oxide; XO is a portion of ethylene oxide that has 3-6 carbon atoms; M is a hydrogen or an alkali metal or alkaline earth metal; a is an integer from about 1-20; b is an integer from about 5-1500; c is an integer from about 2-700; d is an integer from about 1-15; x is an integer from about 1-8; which comprises the steps of: adding AO to an initiator and catalyst followed by b adding a mixture of EO and XO followed by c adding EO. . A dentifrice composition containing: -55% abrasive that is selected from the group including, but not limited to, anhydrous dicalcium phosphate, calcium carbonate, calcium pyrophosphate, and sodium bicarbonate. -0.6% of a fluorinating agent including, but not limited to, stannous fluoride, sodium fluoride, sodium monofluorophosphate. -10% binders including, but not limited to, karaya gum, USP tragacanth, sodium alginate, Irish moss and methylcellulose. -10% of a peroxygen source including, but not limited to, hydrogen peroxide, percarbonate of sodium. 0-8% surfactants including, but not limited to sodium lauryl sulfate, sodium N-lauryl sarcosinate; sodium dioctyl sulfosuccinate. 0-5% block copolymers of EO and PO. 5-50% humectants including, but not limited to glycerin, propylene glycol; sorbitol; polyethylene glycol. 5-70% polyoxyalkylene compound having the formula: I- [(AO) a- [(EO) b (XO) c] - (EO) d-M] x; wherein: I is an initiator or a mixture of initiators having at least one substituent selected from the group including, but not limited to OH, NH2 or COOH; AO is an alkylene oxide of 2-6 carbons or a mixture of alkylene oxides of 2-6 carbons arranged randomly or in a block sequence; EO is ethylene oxide; XO is a portion of alkylene oxide having 3-6 carbon atoms; M is hydrogen or alkali metal or alkaline earth metal; a is an integer from about 1-20; b is an integer from about 5-1500; c is an integer from about 2-700; d is an integer from about 1-15; x is an integer from about 1-8; The dentifrice composition of claim 5, wherein the initiator I is propylene glycol, AO 'is ethylene oxide or ethylene oxide and propylene oxide, XO is propylene oxide, M is H, a is 1-10, b is 5-500, c is 1-250, d is 1-10 and x is 2-3. The dentifrice composition of claim 5, wherein the initiator I is propylene glycol, AO is ethylene oxide or ethylene oxide and propylene oxide, XO is propylene oxide, M is H, a is 2-8, b is 7. -16, c is 1-10, d is 1-5 and x is 2.
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US08775235 | 1996-12-30 |
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