IE911002A1 - Novel surfactants and surfactant compositions - Google Patents
Novel surfactants and surfactant compositionsInfo
- Publication number
- IE911002A1 IE911002A1 IE100291A IE100291A IE911002A1 IE 911002 A1 IE911002 A1 IE 911002A1 IE 100291 A IE100291 A IE 100291A IE 100291 A IE100291 A IE 100291A IE 911002 A1 IE911002 A1 IE 911002A1
- Authority
- IE
- Ireland
- Prior art keywords
- ammonium
- group
- alkyl
- carbon atoms
- detergent composition
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 114
- 239000004094 surface-active agent Substances 0.000 title claims abstract description 38
- 150000004985 diamines Chemical class 0.000 claims abstract description 20
- 125000002467 phosphate group Chemical class [H]OP(=O)(O[H])O[*] 0.000 claims abstract 3
- -1 aliphatic amines Chemical class 0.000 claims description 61
- 125000004432 carbon atom Chemical group C* 0.000 claims description 32
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 25
- 239000003599 detergent Substances 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 21
- 150000001412 amines Chemical class 0.000 claims description 18
- 125000005263 alkylenediamine group Chemical class 0.000 claims description 17
- 150000001875 compounds Chemical class 0.000 claims description 17
- 125000001165 hydrophobic group Chemical group 0.000 claims description 17
- 125000003342 alkenyl group Chemical group 0.000 claims description 16
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 14
- 239000007859 condensation product Substances 0.000 claims description 14
- 125000005210 alkyl ammonium group Chemical group 0.000 claims description 13
- 229910052783 alkali metal Inorganic materials 0.000 claims description 10
- 150000001340 alkali metals Chemical class 0.000 claims description 10
- 150000003863 ammonium salts Chemical class 0.000 claims description 10
- 239000006071 cream Substances 0.000 claims description 10
- 239000000243 solution Substances 0.000 claims description 10
- 239000000344 soap Substances 0.000 claims description 9
- 125000002947 alkylene group Chemical group 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 8
- 239000000551 dentifrice Substances 0.000 claims description 7
- 239000002324 mouth wash Substances 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- 239000002453 shampoo Substances 0.000 claims description 7
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 229910052700 potassium Inorganic materials 0.000 claims description 6
- 239000011591 potassium Substances 0.000 claims description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 230000000694 effects Effects 0.000 claims description 4
- 230000007794 irritation Effects 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- 239000011734 sodium Substances 0.000 claims description 4
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 claims description 4
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 3
- DJEQZVQFEPKLOY-UHFFFAOYSA-N N,N-dimethylbutylamine Chemical compound CCCCN(C)C DJEQZVQFEPKLOY-UHFFFAOYSA-N 0.000 claims description 3
- 229910052744 lithium Inorganic materials 0.000 claims description 3
- VMOWKUTXPNPTEN-UHFFFAOYSA-N n,n-dimethylpropan-2-amine Chemical compound CC(C)N(C)C VMOWKUTXPNPTEN-UHFFFAOYSA-N 0.000 claims description 3
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 claims description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-O butylazanium Chemical compound CCCC[NH3+] HQABUPZFAYXKJW-UHFFFAOYSA-O 0.000 claims 2
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 claims 1
- 238000005187 foaming Methods 0.000 abstract description 8
- 206010040880 Skin irritation Diseases 0.000 abstract description 2
- 239000004480 active ingredient Substances 0.000 abstract description 2
- 230000036556 skin irritation Effects 0.000 abstract description 2
- 231100000475 skin irritation Toxicity 0.000 abstract description 2
- 239000006260 foam Substances 0.000 description 33
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 28
- 210000003491 skin Anatomy 0.000 description 27
- 239000000194 fatty acid Substances 0.000 description 23
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 21
- 239000002253 acid Substances 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 20
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 16
- 229910019142 PO4 Inorganic materials 0.000 description 16
- 235000021317 phosphate Nutrition 0.000 description 16
- 235000014113 dietary fatty acids Nutrition 0.000 description 15
- 229930195729 fatty acid Natural products 0.000 description 15
- 239000003995 emulsifying agent Substances 0.000 description 14
- 239000004615 ingredient Substances 0.000 description 14
- 235000019441 ethanol Nutrition 0.000 description 13
- 239000010452 phosphate Substances 0.000 description 13
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
- 239000004166 Lanolin Substances 0.000 description 12
- 235000019388 lanolin Nutrition 0.000 description 12
- 229940039717 lanolin Drugs 0.000 description 12
- TVACALAUIQMRDF-UHFFFAOYSA-N dodecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCOP(O)(O)=O TVACALAUIQMRDF-UHFFFAOYSA-N 0.000 description 11
- 150000004665 fatty acids Chemical class 0.000 description 11
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 10
- NSOXQYCFHDMMGV-UHFFFAOYSA-N Tetrakis(2-hydroxypropyl)ethylenediamine Chemical compound CC(O)CN(CC(C)O)CCN(CC(C)O)CC(C)O NSOXQYCFHDMMGV-UHFFFAOYSA-N 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical class OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 9
- 235000011187 glycerol Nutrition 0.000 description 9
- 150000002430 hydrocarbons Chemical group 0.000 description 9
- 239000002562 thickening agent Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 8
- 239000006210 lotion Substances 0.000 description 8
- 239000003974 emollient agent Substances 0.000 description 7
- 230000001815 facial effect Effects 0.000 description 7
- 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 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 229940099367 lanolin alcohols Drugs 0.000 description 6
- 229920001223 polyethylene glycol Polymers 0.000 description 6
- 239000003380 propellant Substances 0.000 description 6
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 6
- 239000000600 sorbitol Substances 0.000 description 6
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 5
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 5
- 125000000129 anionic group Chemical group 0.000 description 5
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 5
- 229940012017 ethylenediamine Drugs 0.000 description 5
- 150000002191 fatty alcohols Chemical class 0.000 description 5
- 239000003205 fragrance Substances 0.000 description 5
- 239000000499 gel Substances 0.000 description 5
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 5
- 229940051866 mouthwash Drugs 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 235000019198 oils Nutrition 0.000 description 5
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 229920001451 polypropylene glycol Polymers 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 4
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 4
- 239000000443 aerosol Substances 0.000 description 4
- 239000003945 anionic surfactant Substances 0.000 description 4
- 235000013871 bee wax Nutrition 0.000 description 4
- 239000012166 beeswax Substances 0.000 description 4
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Natural products 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 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 4
- 235000013772 propylene glycol Nutrition 0.000 description 4
- 238000011200 topical administration Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229920002125 Sokalan® Polymers 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 235000021120 animal protein Nutrition 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 235000012000 cholesterol Nutrition 0.000 description 3
- 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 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 231100000344 non-irritating Toxicity 0.000 description 3
- UHGIMQLJWRAPLT-UHFFFAOYSA-N octadecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCCCOP(O)(O)=O UHGIMQLJWRAPLT-UHFFFAOYSA-N 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 3
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 3
- 229960003415 propylparaben Drugs 0.000 description 3
- 229930195734 saturated hydrocarbon Natural products 0.000 description 3
- 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 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
- 230000000699 topical effect Effects 0.000 description 3
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 3
- 229920001285 xanthan gum Polymers 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
- ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 206010013786 Dry skin Diseases 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000005639 Lauric acid Substances 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- BPEPKIRUVOZJDQ-UHFFFAOYSA-N OP(O)(=O)OCCCCCCCCCC=C Chemical compound OP(O)(=O)OCCCCCCCCCC=C BPEPKIRUVOZJDQ-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 229920001214 Polysorbate 60 Polymers 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000004164 Wax ester Substances 0.000 description 2
- 239000003082 abrasive agent Substances 0.000 description 2
- 150000008051 alkyl sulfates Chemical class 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 239000003242 anti bacterial agent Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- ILRSCQWREDREME-UHFFFAOYSA-N dodecanamide Chemical compound CCCCCCCCCCCC(N)=O ILRSCQWREDREME-UHFFFAOYSA-N 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000013355 food flavoring agent Nutrition 0.000 description 2
- 235000003599 food sweetener Nutrition 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- ZUVCYFMOHFTGDM-UHFFFAOYSA-N hexadecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCOP(O)(O)=O ZUVCYFMOHFTGDM-UHFFFAOYSA-N 0.000 description 2
- 239000003906 humectant Substances 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 2
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 2
- 229960002216 methylparaben Drugs 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 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 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 125000001117 oleyl 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])=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])[H] 0.000 description 2
- SSZBUIDZHHWXNJ-UHFFFAOYSA-N palmityl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCC SSZBUIDZHHWXNJ-UHFFFAOYSA-N 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 235000011007 phosphoric acid Nutrition 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- WBHHMMIMDMUBKC-QJWNTBNXSA-M ricinoleate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O WBHHMMIMDMUBKC-QJWNTBNXSA-M 0.000 description 2
- 229940066675 ricinoleate Drugs 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 230000037394 skin elasticity Effects 0.000 description 2
- 238000003892 spreading Methods 0.000 description 2
- 239000003765 sweetening agent Substances 0.000 description 2
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 2
- 239000000606 toothpaste Substances 0.000 description 2
- 229940034610 toothpaste Drugs 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 235000019386 wax ester Nutrition 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 description 1
- JQJSFAJISYZPER-UHFFFAOYSA-N 1-(4-chlorophenyl)-3-(2,3-dihydro-1h-inden-5-ylsulfonyl)urea Chemical compound C1=CC(Cl)=CC=C1NC(=O)NS(=O)(=O)C1=CC=C(CCC2)C2=C1 JQJSFAJISYZPER-UHFFFAOYSA-N 0.000 description 1
- KYUPIHBUKDNZKE-UHFFFAOYSA-N 1-amino-3-methylbutan-2-ol Chemical compound CC(C)C(O)CN KYUPIHBUKDNZKE-UHFFFAOYSA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical class CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- XVUFFCCIYYUUBP-UHFFFAOYSA-N 10-oxo-10-propoxydecanoic acid Chemical compound CCCOC(=O)CCCCCCCCC(O)=O XVUFFCCIYYUUBP-UHFFFAOYSA-N 0.000 description 1
- UCLORACXEUJGBI-UHFFFAOYSA-N 15-methylhexadecyl dihydrogen phosphate Chemical compound CC(C)CCCCCCCCCCCCCCOP(O)(O)=O UCLORACXEUJGBI-UHFFFAOYSA-N 0.000 description 1
- XFOQWQKDSMIPHT-UHFFFAOYSA-N 2,3-dichloro-6-(trifluoromethyl)pyridine Chemical compound FC(F)(F)C1=CC=C(Cl)C(Cl)=N1 XFOQWQKDSMIPHT-UHFFFAOYSA-N 0.000 description 1
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- 229920005862 polyol Polymers 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- NEOZOXKVMDBOSG-UHFFFAOYSA-N propan-2-yl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OC(C)C NEOZOXKVMDBOSG-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 230000037307 sensitive skin Effects 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 230000036620 skin dryness Effects 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000012177 spermaceti Substances 0.000 description 1
- 229940084106 spermaceti Drugs 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 239000000271 synthetic detergent Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- BORJONZPSTVSFP-UHFFFAOYSA-N tetradecyl 2-hydroxypropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)C(C)O BORJONZPSTVSFP-UHFFFAOYSA-N 0.000 description 1
- KRIXEEBVZRZHOS-UHFFFAOYSA-N tetradecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCCCOP(O)(O)=O KRIXEEBVZRZHOS-UHFFFAOYSA-N 0.000 description 1
- DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
- ICUTUKXCWQYESQ-UHFFFAOYSA-N triclocarban Chemical compound C1=CC(Cl)=CC=C1NC(=O)NC1=CC=C(Cl)C(Cl)=C1 ICUTUKXCWQYESQ-UHFFFAOYSA-N 0.000 description 1
- 229960003500 triclosan Drugs 0.000 description 1
- 125000002889 tridecyl 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])[H] 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl 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])[H] 0.000 description 1
- 239000012178 vegetable wax Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0094—High foaming compositions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/11—Esters of phosphoric acids with hydroxyalkyl compounds without further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/34—Derivatives of acids of phosphorus
- C11D1/345—Phosphates or phosphites
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/30—Amines; Substituted amines ; Quaternized amines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Seal Device For Vehicle (AREA)
Abstract
Disclosed are novel low skin irritation surfactants and surfactant compositions which are high in foaming properties containing, as an active ingredient, a diamine monoalkyl phosphate salt.
Description
NOVEL SURFACTANTS AND SURFACTANT COMPOSITIONS
TECHNICAL FIELD 5 The present invention relates to novel low skin irritation surfactants and surfactant compositions which are high in foaming properties containing, as an active ingredient, a diamine monoalkyl phosphate salt.
BACKGROUND OF THE INVENTION
Soaps, detergents and abrasives have long been used to cleanse the skin on various portions of the body. Anionic surfactants such as alkyl sulfates, polyoxyethylene alkyl sulfates, alkylbenzene sulfonates and a-olefin sulfonates have been widely used as the surfactant component for many cleansers.
It is known that such anionic surfactants are adsorbed and thereby remain on the skin surface to cause dryness and scaling of the epidermis, or skin chapping and roughness, 1f they are used continually. Thus, skin troubles such as roughness of hands are apt to be caused by the use of detergents. Skin roughness can be a precursor of 2θ more severe skin troubles such as eczema. Thus, there is an urgent need to eliminate this disadvantage.
Nonionic surfactants, on the other hand, cause little or no skin dryness or roughness. However, they do not have the same advantageous properties of foaming and detergency as anionic surfactants. It has, 25 therefore, not been suitable to incorporate nonlonic surfactants into cleansing compositions as the primary detergent component.
Phosphoric acid esters have been known as anionic surfactants, generally as mono- and diesters, or mixtures thereof. However, in general, their water solubilities and foaming properties are not very good.
European Patent No. 265 702 published May 4, 1988 discloses transparent or semi-transparent cosmetic compositions containing a monoalkyl phosphate, water, oil and alcohol for skin treatment. The oils and alcohols are used to obtain clarity. U.S. Patent 4,573,749 to McIntosh, issued June 28, 1988 discloses monoamine alkyl phosphates having antimicrobial activity. U.S. Patent 4,290,904 to Poper et al., issued September 22, 1981, U.K. Patent No. 1,513,053, published June 7, 1978 and European Patent 023 978, published February 18, 1981 disclose cosmetic and toiletry preparations containing alkoxylated
-2alkylene diamines. U.S. Patent 4,476,043, 4,476,044 and 4,476,045 to O'Lenick, all issued October 9, 1984 and U.S. Patent 4,477,372 to O'Lenlck, issued October 16, 1984 disclose substantially non-aqueous surfactants containing an organic sulfate, mineral oil and an alkoxyl5 ated amine. However, none of these references disclose the use of a diamine alkyl phosphate surfactant.
Monoalkyl phosphate salts have also been disclosed as useful surfactants in U.S. Patent 4,139,485 to Imokawa et al., issued February 13, 1979. However, these surfactants form turbid aqueous solu10 tions unless they contain other solvents (e.g., solubilizing agents). Further, the rheology of these salts limits the variety of formulations which can be made with aesthetically pleasing characteristics.
It has been discovered that certain novel diamine monoalkyl phosphate salts as well as certain transparent and stable surfactant compositions containing these salts readily enable the preparation of stable non-pressurized, aerated foams. These foams possess good cleansing power and detergency, are mild and non-irritating, and leave little, if any, residual film remaining on the cleansed surface of the skin. These compositions are homogeneous in nature, can be structured to be wet or dry, stable or fastbreaking, and are aesthetically suitable for use in a wide variety of personal care products.
One of the principal purposes of this invention is to describe the preparation of an aqueous skin cleansing composition made from the novel diamine monoalkyl phosphate salts of the present invention which will produce a usable foam from a hand-held, squeezable foam dispensing device, as well as from an aerosol device and further which will not render the device unusable by, for example, clogging the device.
Another object of this Invention is to provide surfactants and foam-producing surfactant compositions which produce relatively stable
3q or collapsible foams. A preferred embodiment of this invention is to provide skin cleansing foams of low density.
Another object of this invention is to provide surfactants and foaming compositions with creamy lather, good skin feel and good rinsabllity and which retains skin elasticity.
Another object of this invention is to provide a surfactant and surfactant composition which is mild and non-irritating to skin and eyes and which does not require the use of propellants, thereby avoiding the danger of explosion or corrosion of the container.
-3Still another object of this invention is to provide a foam producing composition such that if placed in a hand-held, foam dispensing device having deformable walls, the amount of force required to produce the foam is not excessive (i.e., less than about 15 psi) and is readily usable by the average person.
These objectives as well as others apparent to those skilled in the art are obtained with the compounds and compositions described herein.
SUMMARY OF THE INVENTION
This invention comprises diamine monoalkyl phosphate salts having low irritation effect to human skin of the formula:
0Xx
R0--P--0X2
H wherein R is a hydrophobic group or the condensation product of a hydrophobic group with ethylene oxide, preferably R is alkyl or alkenyl having an average of from about 10 to 18 carbon atoms, and wherein Xx and X2 are independently selected from the group consisting of hydrogen, alkali metal, ammonium, substituted ammonium (e.g., alkoxylated ammonium, alkyl ammonium, alkoxylated aliphatic amines, polyethoxylated amines) and alkylene diamine, provided that at least one of Xx and X2 is a totally hydroxyalkylated alkylene diamine.
Also disclosed are compositions comprising these diamine monoalkyl phosphate salts.
Sesquialkyl phosphate salts are not within the scope of the present invention.
All parts, percentages and ratios used herein are by weight and all measurements are at 25’C unless otherwise indicated.
DETAILED DESCRIPTION OF THE INVENTION
The surfactant compounds of the present invention are of the formula:
0Xx
R0--P--0X2 ii
O wherein R is a hydrophobic group or the condensation product of a hydrophobic group with ethylene oxide, preferably R is alkyl or alkenyl having an average of from about 10 to 18 carbon atoms, and wherein Xx and X2 are independently selected from the group consisting of hydrogen, alkali metal, ammonium, substituted ammonium (e.g.,
-4alkoxylated ammonium, alkyl ammonium, alkoxylated aliphatic amines, polyethoxylated amines) and alkylene diamine, provided that at least one of Χχ and X2 is a totally hydroxy alkylatedalkylene diamine.
Monoalkyl phosphate salts in the present invention can be pre5 pared, for example, by a known process wherein a long chain aliphatic alcohol (or the condensation product of a long chain aliphatic alcohol with ethylene oxide) is reacted with a phosphatizing agent such as phosphoric anhydride or phosphorus oxychloride. It is recognized that the dialkyl phosphate can be by-produced by this process and which possess poor water-solubility or foaming properties. Such dialkyl phosphates have the formula:
OX3
RO--P--OR
II wherein R is a hydrophobic group or the condensation product of a hydrophobic group with ethylene oxide, preferably R 1s alkyl or alkenyl having an average of from about 10 to 18 carbon atoms, and wherein X3 1s selected from the group consisting of hydrogen, alkali metal, ammonium, substituted ammonium (e.g., alkoxylated ammonium, alkyl ammonium, alkoxylated aliphatic amines, polyethoxylated amines) and alkylene diamine. Preferably, R is the condensation product of a hydrophobic group with from about 1 to about 10 moles and preferably from about 1 to about 4 moles of ethylene oxide.
Preferably, the weight ratio of the diamine monoalkyl phosphate salt to the dialkyl phosphate salt is from about 99:1 to about 70:30, respectively, preferably from about 100:0 to about 90:10, most preferred is a ratio of substantially 100:0. However, unlike monoamine, alkali, or ammonium phosphate salts, these diamine phosphates of the diester are uniquely water-soluble and, therefore, will not interfere as much with the devices and formulations described herein.
The surfactants of the present invention are particularly useful in detergent products which are directly contacted with the skin for a long time such as facial cleansers, shampoos, and solid synthetic detergent toilet bars, because they have a characteristic, excellent foaming power and skin roughness is not caused. The surfactants can also be used as ingredients of dish-washing liquid detergents, powder detergents and dentifrices and are particularly useful compositions where a clear and non-turbid composition is desirable.
-5The saturated and unsaturated hydrocarbon groups having an average carbon number of 10-18 (R) are straight chain, branched or allcyclic hydrocarbons such as decyl, undecyl, dodecyl, tri decyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, and octadecyl groups and corresponding olefinically unsaturated groups. Those hydrocarbon groups are contained in the compositions singly or in the form of a combination of several groups. Saturated hydrocarbon groups of an average carbon number of 10 to 14 and unsaturated hydrocarbon groups of an average carbon number of 16 are particularly preferred. Also preferred for use herein are the saturated or unsaturated hydrocarbon groups wherein said hydrocarbon groups possess from about 1 to about 10 units and preferably from about 1 to about 4 units of ethylene oxide per molecule.
The preferred alkali metals for Xj and X2 according to the invention, are, for example, lithium, sodium and potassium.
The alkyl ammonium or substituted alkylammonium for Xx and X2 according to the invention, are cations produced from amines used for neutralization of the corresponding phosphoric acids by salt formation after the neutralization step in the process for preparing monoalkyl phosphate salts in the present invention. The corresponding amines are primary, secondary and tertiary amines having alkyl groups of 1 to 4 carbon atoms which can be further substituted, particularly by hydroxyl groups. As the amines, there can be mentioned, for example, dimethylmonoethanol amine, methyl diethanolamine, trimethylamine, triethylamine, dlbutylamlne, butyldimethyl amine, monoethanolamine, diethanolamine, triethanolamine, isopropyl dimethyl amine and isopropylethanolamine. Preferred amines are monoethanolamine, diethanolamine and triethanolamine. A particularly preferred amine is triethanolamine. Other useful amines Include arginine, lysine, mono-, di- or tr1isopropanol amine, N,N-tris(hydroxymethyl) ami nomethane, diglycol amine, glucamlne, aminomethyl propanol, and aminomethylpropanediol. Also useful in the present invention are the copolymers derived from the addition of ethylene oxide and propylene oxide available as Tetronic· and Tetronlc R· available from BASF Corporation and the polyethoxylated amines available as the Ethomeen· series available from Armak Corporation.
-6The alkylene diamine, according to the present Invention has the general formula:
R1R2N--R3--NR4Rs, in which Rx, R2, R4 and R5 are independently hydrogen, an alkyl group having 1 to 4 carbon atoms or a hydroxylalkyl or di hydroxyalkyl group having 1 to 4 carbon atoms or R4 and Rs jointly form a saturated 5 or 6 membered heterocyclic ring, which can be substituted by an oxo- or hydroxyalkyl group and R3 represents an alkylene or hydroxyalkylene group having 2 to 4 carbon atoms, provided that at least one of Rx, R2, R3, R4 and Rs contain at least one hydroxy group.
These compounds are fully disclosed in U.K. Patent 1,513,053, published June 7, 1978.
A particular amine class that is useful herein is an N,N-tetrakis (hydroxyalkyl) ethylene diamine having the formula:
R [HO--CH--CH2]nX N--Rx--N [HO--CH--CH2]n '
R
R [CH2--CHOH]n [CH2--CHOH]n
R wherein R3 is alkylene having two to four carbon atoms, R is hydrogen or an alkyl group having one to six carbon atoms and n is from one to four. The foregoing diamine preferably has a molecular weight of under about 1700, preferably under about 1200, even more preferably under about 800 and most preferably under about 500.
Although other examples will also be given hereinafter, the tetrakls (hydroxyalkyl) ethylene diamine 1s best exemplified by the compound N,N,Ν',N'-tetrakis(2-hydroxypropyl)-ethylened1 amine, obtainable commercially under the trademark Quadrol or Neutrol TE (both available from BASF Wyandotte Company).
Examples of diamine monoalkyl phosphate salts useful in the present invention include, but are not limited to, tetrahydroxypropyl ethylened1 amine monococoylphosphate, tetrahydroxypropyl ethylenedi ami ne monolaurylphosphate, tetrahydroxypropylethylenediamine (monoethoxylated) monolaurylphosphate, tetrahydroxypropyl ethylenedi ami ne monoi sostearylphosphate, tetrahydroxypropyl ethylenedi ami ne monostearylphosphate, tetrahydroxypropylethylenediamine (monoethoxylated) monostearylphosphate,
-7tetrahydroxypropylethylenedi ami ne monomyr1stylphosphate, tetrahydroxypropyl ethylened i ami ne (monoethoxylated) monomyrlstylphosphate, tetrahydroxypropyl ethylenedi ami ne monooleoylphosphate, tetrahydroxypropylethylenediamine monopalmiltylphosphate, tetrahydroxypropyl ethylenedi ami ne (monoethoxylated) monopalmiltylphosphate, tetrahydroxypropyl ethylenediami ne monocaprylphosphate, tetrahydroxypropyl ethylenedi amine (monoethoxylated) monocaprylphosphate, tetrahydroxypropyl ethylenedi ami ne monoundecylenylphosphate, tetrahydroxypropyl ethylenediamine monotridecylenylphosphate, tetrahydroxypropyl ethylenedi ami ne mono(methylmyri styl)phosphate, tetrahydroxypropyl ethylenedi ami ne mono(1sopropyl1auryl) phosphate, tetrahydroxypropyl ethylenedi ami ne mono(1sodecylneopentyl) phosphate, tetrahydroxypropyl ethylenediamine monocetyl phosphate, and tetrahydroxypropyl ethylenedi ami ne mono(1sopropylmyri styl) phosphate.
COMPOSITIONS
The compositions of the present Invention comprise:
(a) from about 0.1% to about 99% of one or more of a diamine monoalkyl phosphate salt of the present invention; and (b) from about 1.0% to about 99.0% of a detergent carrier. Preferred compositions comprise a mixture of the diamine monoalkyl phosphate salts wherein R is selected from the group consisting of C12 to C14 alkyl or alkenyl and Cie to Cie alkyl or alkenyl (or the condensation porduct of these moieties with from about 1 to about 10 moles of ethylene oxide) and wherein said salts are present in a ratio of from about 80:20 to about 20:80, preferably from about 60:40 to about 40:60 and most preferably from about 55:45 to about 45:55, respectively.
The compositions of the present invention can be administered topically, i.e., by the direct laying on or spreading of the composition on epidermal or epithelial tissue. Such compositions can be formulated as foams, lotions, creams, ointments, solutions, gels or solids. A highly preferred composition contains the monoalkyl phosphate salt in a soap matrix (i.e., liquid and solid). These topical compositions comprise a safe and effective amount, usually from about 0.1% to about 99%, and preferably from about 1% to about 10%, of the
-8monoalkyl phosphate salt. Bar compositions generally contain very high levels i.e., above 80%, of the diamine monoalkyl phosphate salt. Generally, the carrier is either organic in nature or a solution or an aqueous emulsion and is capable of having the diamine monoalkyl phosphate salt dispersed, dissolved or suspended therein. The carrier can include pharmaceutically-acceptable emollients, skin penetration enhancers, coloring agents, fragrances, emulsifiers, thickening agents, and solvents. A more detailed description of such forms follows:
1. Lotions.
The lotions can comprise a safe and effective amount of the monoalkyl phosphate salt; from about 0.1% to about 25%, preferably from about 3% to about 15%, of an emollient; the balance being water, a C2 or C3 alcohol, or a mixture of water and the alcohol. Examples of suitable emollients are as follows:
1. Hydrocarbon oils and waxes. Examples are mineral oil, petrolatum, paraffin, ceresln, ozokerite, microcrystalline wax, polyethylene, and perhydrosqualane.
2. Silicone oils, such as polydimethyl siloxanes, methylphenyl20 polysiloxanes, water-soluble and alcohol-soluble silicone-glycol copolymers.
3. Triglyceride fats and oils, such as those derived from vegetable, animal and marine sources. Examples include castor oil, safflower oil, cotton seed oil, corn oil, olive oil, cod liver oil, almond oil, avocado oil, palm oil, sesame oil, and soybean oil.
4. Acetoglyceride esters, such as acetylated monoglycerides.
. Ethoxylated glycerides, such as ethoxylated glyceryl monostearate.
6. Alkyl esters of fatty acids having 10 to 20 carbon atoms. 30 Methyl, isopropyl and butyl esters of fatty acids are especially useful herein. Examples include hexyl laurate, isohexyl laurate, isohexyl palmitate, isopropyl palmitate, decyl oleate, isodecyl oleate, hexadecyl stearate, decyl stearate, isopropyl isostearate, diisopropyl adipate, diisohexyl adipate, dlhexyldecyl adipate, diiso35 propyl sebacate, lauryl lactate, myristyl lactate, and cetyl lactate.
7. Alkenyl esters of fatty acids having 10 to 20 carbon atoms. Examples thereof include oleyl myristate, oleyl stearate, and oleyl oleate.
-98. Fatty acids having 9 to 22 carbon atoms. Suitable examples include pelargonic, lauric, myristic, palmitic, stearic, isostearic, hydroxystearic, oleic, linoleic, ricinoleic, arachidonic, behenic, and eruclc acids.
9. Fatty alcohols having 10 to 22 carbon atoms. Lauryl, myristyl, cetyl, hexadecyl, stearyl, isostearyl, hydroxystearyl, oleyl, ricinoleyl, behenyl, erucyl, and 2-octyl dodecyl alcohols are examples of suitable fatty alcohols.
. Fatty alcohol ethers. Ethoxylated fatty alcohols of 10 to 20 10 carbon atoms include the lauryl, cetyl, stearyl, isostearyl, oleyl, and cholesterol alcohols having attached thereto from 1 to 50 ethylene oxide groups or 1 to 50 propylene oxide groups, or a mixture thereof.
11. Ether-esters such as fatty acid esters of ethoxylated fatty alcohols.
12. Lanolin and its derivatives. Lanolin, lanolin oil, lanolin wax, lanolin alcohols, lanolin fatty acids, isopropyl lanolate, ethoxylated lanolin, ethoxylated lanolin alcohols, ethoxylated cholesterol, propoxy1ated lanolin alcohols, acetylated lanolin, acetylated lanolin alcohols, lanolin alcohols linoleate, lanolin alcohols ricinoleate, acetate of lanolin alcohols ricinoleate, acetate of ethoxylated alcohols-esters, hydrogenolysis of lanolin, ethoxylated hydrogenated lanolin, ethoxylated sorbitol lanolin, and liquid and semisolid lanolin absorption bases are illustrative of emollients derived from lanolin.
13. Polyhydric alcohols and polyether derivatives. Propylene glycol, dipropylene glycol, polypropylene glycol (M.W. 2000-4000), polyoxyethylene polyoxypropylene glycols, polyoxypropylene polyoxyethylene glycols, glycerol, ethoxylated glycerol, propoxylated glycerol, sorbitol, ethoxylated sorbitol, hydroxypropyl sorbitol, poly30 ethylene glycol (M.W. 200-6000), methoxy polyethylene glycols, poly[ethylene oxide] homopolymers (M.W. 100,000-5,000,000), polyalkylene glycols and derivatives, hexylene glycol (2-methyl-2,4-pentanediol),
1.3- butylene glycol, 1,2,6-hexanetriol, ethohexadiol USP (2-ethyl1.3- hexanediol), C15-C1S vicinal glycol, and polyoxypropylene deriva35 tives of trimethylolpropane are examples thereof.
14. Polyhydric alcohol esters. Ethylene glycol mono- and di-fatty acid esters, diethylene glycol mono- and di-fatty acid esters, polyethylene glycol (M.W. 200-6000) mono- and di-fatty acid esters, propylene glycol mono- and di-fatty acid esters, polypropylene
-1010 glycol 2000 monooleate, polypropylene glycol 2000 monostearate, ethoxylated propylene propylene glycol monostearate, glyceryl monoand di-fatty acid esters, polyglycerol poly-fatty acid esters, ethoxylated gylceryl monostearate, 1,3-butylene glycol monostearate,
1,3-butylene glycol distearate, polyoxyethylene polyol fatty acid ester, sorbitan fatty acid esters, and polyoxyethylene sorbitan fatty acid esters are satisfactory polyhydric alcohol esters.
. Wax esters, such as beeswax, spermaceti, myristyl myristate, stearyl stearate.
16. Beeswax derivatives, e.g., polyoxyethylene sorbitol beeswax. These are reaction products of beeswax with ethoxylated sorbitol of varying ethylene oxide content, forming a mixture of ether-esters.
17. Vegetable waxes including carnauba and candelilla waxes.
18. Phospholipids, such as lecithin and derivatives.
19. Sterols. Cholesterol, cholesterol fatty acid esters are examples thereof.
. Amides, such as fatty acid amides, ethoxylated fatty acid amides, solid fatty acid alkanolamides.
The lotions further comprise from about 1% to about 10%, preferably from about 2% to about 5%, of an emulsifier. The emulsifiers can be nonionic, anionic or cationic. Examples of satisfactory nonionic emulsifiers include fatty acid alcohols having 10 to 20 carbon atoms, fatty alcohols having 10 to 20 carbon atoms condensed with 2 to 20 moles of ethylene oxide or propylene oxide, alkyl phenols with 6 to 12 carbon atoms 1n the alkyl chain condensed with 2 to 20 moles of ethylene oxide, mono- and d1-fatty acid esters of ethylene oxide, mono- and di-fatty acid esters of ethylene glycol wherein the fatty acid moiety contains from 10 to 20 carbon atoms, diethylene glycol, polyethylene glycols of molecular weight 200 to 6000, propylene glycols of molecular weight 200 to 3000, glycerol, sorbitol, sorbitan, polyoxyethylene sorbitol, polyoxyethylene sorbitan and hydrophilic wax esters. Suitable anionic emulsifiers include the fatty acid soaps, e.g. sodium, potassium and triethanolamine soaps, wherein the fatty acid moiety contains from 10 to 20 carbon atoms. Other suitable anionic emulsifiers Include the akali metal, ammonium or substituted ammonium alkyl sulfates, alkyl aryl sulfonates, and alkyl ethoxy ether sulfonates having 10 to 30 carbon atoms in the alkyl moiety. The alkyl ethoxy ether sulfonates contain from 1 to 50 ethylene oxide
-11units. However, it is recognized that certain anionic emulsifiers can result in a turbid formulation, and hence, anionic emulsifiers are less preferred for use herein.
The balance of the lotion is water or a C2 or C3 alcohol, or a 5 mixture of water and the alcohol. The lotions are formulated by simply admixing all of the components together. Preferably the monoalkyl phosphate salt is dissolved in the mixture. Conventional optional components can be included. One such additive is a thickening agent at a level from about 1% to about 10% of the composition.
Examples of suitable thickening agents include: cross-linked carboxypolymethylene polymers (sufficiently neutralized), magnesium aluminum silicate, carboxymethyl cellulose, hydroxyethyl cellulose, acrylic acid polymers (e.g., Acrysol ICS-I, available from Rohm & Haas Corporation), polyethylene glycols, gum tragacanth, gum kharaya, xanthan gums and bentonite. Cationic polymers, such as cationic guar gum, are not preferred for use herein.
2. Creams.
Compositions of the present invention also can be formulated in a cream form. The creams comprise safe and effective amounts of the monoalkyl phosphate salt; from about 0.1% to 95%, preferably from about 10% to about 25%, of an emollient; the balance being water. The emollients above described can also be used in the cream compositions. Optionally, the cream form contains a suitable emulsifier, as previously described. When an emulsifier is included, it is 1s the compo25 sition at a level from about 3% to about 50%, preferably from about 5% to about 20%.
3. Solutions.
The compositions of this invention can also be formulated as a solution. The solution form comprises a safe and effective amount of the monoalkyl phosphate salt, usually at least about 0.01% up to about 50% and preferably about 0.1% to about 10%; the balance being water or a suitable organic solvent. Suitable organic materials useful as the solvent or a part of a solvent system are as follows: propylene glycol, polyethylene glycol (M.W. 200-1000), polypropylene glycol (M.W. 425-2025), butylene glycol, glycerine, sorbitol esters, 1,2,6hexanetriol, ethanol, isopropanol, diethyl tartrate, butanediol, and mixtures thereof.
-12These solutions can be applied to the skin as is, or else can be formulated into, for example, squeeze devices described below or as an aerosol and sprayed onto the skin from an aerosol container, or as a mouthwash composition and used as an oral rinse. The aerosol composi5 tions further comprise from about 25% to about 80%, preferably from about 30% to about 50%, of suitable propellants. Examples of such propellants are the chlorinated, fluorinated and chlorofluorinated lower molecular weight hydrocarbons. Nitrous oxide, carbon dioxide, butane, and propane can also be used as propellant gases. These propellants are used at a level sufficient to expel the contents of the container.
Squeeze foamer packages are well known as exemplified by the disclosures 1n the following patents that are incorporated herein by reference. U.S. Pat. Nos. 3,709,437, Wright, issued Jan. 9, 1973;
3,937,364, Wright, issued Feb. 10, 1976; 4,022,351, Wright, issued May
, 1977; 4,147,306, Bennett, issued Apr. 3, 1979; 4,184,615, Wright, issued Jan. 22, 1980; 4,598,862, Rice, issued July 8, 1986; and 4,615,467, Grogan et al., issued Oct. 7, 1986; and French Pat. 2,604,622, Verhulst, published Apr. 8, 1988.
The above containers (packages) do not use any propellant and are therefore safe for the consumer and the environment. They create a foam from almost any surfactant composition. Although there is no need to add foam boosters merely for the purpose of stabilizing the foam, such materials can be desirable. In some compositions the use of foam boosters can even be counterproductive since the foam has to break in order for the container to work properly. The composition is placed in the container reservoir (plastic squeeze bottle). Squeezing the container with the hand forces the composition through a foamer head, or other foam producing means, where the composition is mixed with air and then through a homogenizing means that makes the foam more homogeneous and controls the consistency of the foam. The foam is then discharged as a uniform, non-pressurized aerated foam.
The minimum pressure to activate the squeeze foamer is about 1 psig, typically from about 2 psig to about 7 psig. The minimum pressure 1s related to the size of the channels in the dispenser, the viscosity of the composition, etc.
In general, the density of the foam should be between about 0.002 and about 0.25 g/cc, preferably between about 0.01 and about 0.12 g/cc, and more preferably between about 0.02 and about 0.07 g/cc.
-13The carrier liquid 1n a mouthwash is generally a mixture of ethanol and water. The amount of ethanol is generally from about 5% to about 60%, preferably from about 5% to about 25% by weight of the carrier. Water then constitutes the remainder of the carrier liquid mixture. These mouthwash compositions can also contain other optional components such as emulsifying agents as previously described, flavoring agents, sweeteners, and humectants. Other mouthwash formulations and methods for making mouthwashes useful in the present invention are disclosed in U.S. Patent 4,323,551 to Parran, issued April 6, 1982, which is incorporated by reference herein.
4. Gels.
Compositions herein can be formulated into a gel form by simply admixing a suitable thickening agent to the previously described solution compositions. Examples of suitable thickening agents have been previously described with respect to the lotions.
The gelled compositions comprise a safe and effective amount of the monoalkyl phosphate salt, from about 0.5% to about 20%, preferably from about 1% to about 10%, of the thickening agent; the balance being water.
. Solids.
The compositions of this invention can also be formulated in a solid form, e.g., a stick-type composition. Such compositions comprise a safe and effective amount of the monoalkyl phosphate salt and from about 0.01% to about 99%, preferably from about 60% to about 90%, of the previously described emollients. This composition can further comprise from about 0.1% to about 20%, preferably from about 5% to about 15%, of a suitable thickening agent, and optionally emulsifiers and water. Thickening agents previously described with respect to lotions are also suitable herein.
6. Soaps.
The compositions of this invention can also be formulated into a liquid or solid (e.g., bar) soap matrix. Such compositions comprise a safe and effective amount of the monoalkyl phosphate salt ranging from about 0.1% to about 99%; and from about 1% to about 99% of an exci pi 35 ent such as those previously described. Optionally, the soap contains a suitable emulsifier as previously described. When an emulsifier is included, it is in the composition at a level from about 10% to about
50%.
-147. Dentifrices.
The compositions of this Invention can also be formulated as dentifrices. Such dentifrices, especially toothpaste, comprise a safe and effective amount of the monoalkyl phosphate salt ranging from about 0.1% to about 20% by weight of the composition. Toothpaste compositions conventionally contain abrasive materials, sudsing agents, binders, humectants, flavoring and sweetening agents. Suitable dentifrice compositions and the methods of their manufacture useful 1n the present invention are fully set forth in U.S. Patent
3,535,421 to Briner et al., issued October 20, 1970, which is incorporated by reference herein.
8. Shampoos.
Compositions of this invention also can be formulated in a shampoo form. The shampoos comprise a safe and effective amount of the diamine monoalkyl phosphate salt ranging from about 0.1% to about 99%; from about 5% to about 60% of a synthetic surfactant; and the balance water. A secondary surfactant can also be utilized, however, such secondary surfactant should be neutralized by a diamine as described above.
These shampoos can contain a variety of nonessential optional components. Such conventional optional ingredients are well known to those skilled in the art, e.g., preservatives, such as benzyl alcohol, ethyl paraben, propyl paraben and imidazolidlnyl urea; cationic surfactants, such as cetyl trimethyl ammonium chloride, stearyldi25 methyl benzyl ammonium chloride, and di(partially hydrogenated tallow) dimethyl ammonium chloride; thickeners and viscosity modifiers such as diethanol amide of a long-chain fatty acid (e.g. PEG 3 lauramide), block polymers of ethylene oxide and propylene oxide, sodium chloride, sodium sulfate, polyvinyl alcohol, and ethyl alcohol; pH adjusting agents, such as citric acid, succinic acid, phosphoric acid, sodium carbonate; perfumes; dyes; and, sequestering agents, such as di sodium ethylenediamine tetraacetate. Such agents generally are used individually at a level of from about 0.01% to about 10%, preferably from about 0.5% to about 5.0% by weight of the composition.
Additional minor components can be added to the compositions of this invention 1n order to increase their attractiveness, versatility, and shelf-life. Perfumes and water soluble, pharmaceutically acceptable dyes or food colors can be added to enhance the attractiveness of
-15these compositions. Antifungal and antimicrobial agents are useful in preventing mold or bacterial contamination and in increasing the shelf-life of the compositions. Conventional antibacterial agents can be included 1n the present compositions at levels of from about 0.1% to about 4%, preferably from about 0.2% to about 1%. Typical antibacterial agents which are suitable for use herein are 3,4-di- and 3,4' ,5-tribromosalicylanildes; 4,4'-dichloro-3-(trifluoromethyl)carbanilide; 3,4,4'-trichlorocarbanilide; phenoxy ethanol or propanol; chlorhexidene salts; hexamidine salts; Irgasan DP 300 (Triclosan);
salicylic acid; parachlorometaxylenol; Octopirox; and mixtures of these materials. For general purposes skin cleansing compositions having a pH range from about 5.0 to about 8.0 are desirable. If necessary, the pH of these compositions can be adjusted downward using citric or lactic acid. For skin cleansers which deal with more sensitive skin surfaces, such as 1n vaginal and perianal cleansers, a pH of about 6.5 1s desirable. These and other minor modifications can be made without materially altering or departing from the basic concept of this invention.
The nature of the foam produced determines the usefulness of the present compositions. In order for a foam to be useful as a skin cleansing agent, it must have a uniform consistency, good spreadability, and good cleansing ability.
The foamabUlty and wettability characteristics are governed by the surface tension of the skin cleansing composition. The surface tension for the compositions of this invention varies from about 20 to 70 dynes/cm. For general skin cleansing compositions a range of from about 23 to about 50 dynes/cm is preferred. Liquid compositions having a surface tension in the lower portion of this range possess greater spreading and better wetting characteristics with increased foamab111ty. Foamable compositions having higher surface tensions generally provide more stable foams but are also more difficult to cause to foam and require more force to extrude the foam.
The foam-producing skin cleansing compositions of this invention are particularly advantageous in that they leave a minimum amount of surfactant residue on the surface of the skin. This has been achieved in part by utilizing a low percentage of total surfactants in the skin cleansing compositions itself, and by preparing foams with unusually low density. The present compositions provide foam densities provide
ΙΕ 9110θ2
-16good cleansing ability and more importantly, leave a negligible amount of surfactant residue on the surface of the skin upon rinsing or flattening, thereby preserving skin elasticity, and reducing transepiderma 1 moisture loss.
The cleansing ability of these aerated foams is a direct function of the cleansing ability of the surfactant solution itself which produces the foam.
The following non-limiting examples Illustrate embodiments of the subject Invention wherein both essential and optional ingredients are combined. It is to be understood that these examples are for illustrative purposes only and are not to be construed as limiting the scope of the Invention thereto.
EXAMPLE I mole of monolauryl phosphate acid is heated over a steam bath to about 50*C until molten. 1 mole of Ν,Ν,Ν',N'-tetrakis(2-hydroxypropyl)-ethylenediamine (available as Quadrol from BASF Corporation) is heated 1n a separate beaker to 50*C until pourable.
The molten phosphate is slowly added to the N,N,N',N'-tetrakis(2hydroxypropyl)-ethylenediamine. The phosphate is added until a pH of
.0 to 9.0 1s reached (preferably 7.0). The resulting Ν,Ν,Ν',Ν'tetrakis(2-hydroxypropyl)-ethylened1am1ne monolaurylphosphate is then cooled to form a clear, yellow solid.
This solid can be used as a solid bar or as a material to produce liquid cream or gel product.
Application of approximately 0.5 grams to the skin will provide a foaming cleanser possessing good cleansing power and detergency, which is mild and non-irritating, and leaves little, if any, residual film remaining on the cleansed surface of the skin.
Substantially similar results are obtained when the monolauryl phosphate acid is replaced with an equivalent amount of monococoylphosphate acid, monolaurylphosphate acid, monolsostearylphosphate acid, monostearylphosphate acid, monomyristylphosphate acid, monool eoyl phosphate acid, monopalmitylphosphate acid, monocaprylphosphate acid, monoundecylenylphosphate acid, monotridecylenylphosphate acid, mono(methylmyristyl)phosphate acid, mono(isopropyllauryl)phosphate acid, mono(1sodecylneopentyl)phosphate acid, monocetyl phosphate acid, and mono(isopropylmyristyl)phosphate acid and mixtures thereof.
-1710
EXAMPLE II
A facial cleansing composition for topical prepared by combining the following ingredients:
Ingredients
Ν,Ν,Ν',N'-tetrakis(2-hydroxypropyl)ethylenedi amine mono!aurylphosphate Butylene Glycol
Methylparaben Propylparaben
Potassium coco(hydrolysed animal protein)
Glycerin
Aloe Vera
Fragrance
Color
Xanthan gum2 Water 1 Available as Lamepon S from Henkel Corporation 2 Available as Keltrol T from Kelco Corporation administration
Percent w/w
2.500
2.500
0.250
0.150
0.032
2.000
0.500
0.050
0.170
0.050
q.s.
is
E&SMELE HI
A facial cleansing cream composition for topical administration is prepared by combining the following ingredients:
Ingredients Percent w/w
Ν,Ν,Ν',N'-tetrakis(2-hydroxypropyl)ethylenediamine monolaurylphosphate 27.000
Laurie acid 4.000
Ν,Ν,Ν',N'-tetrakis(2-hydroxypropyl)ethylenediamine1 4.000
Carboxyvinyl polymer2 0.200
Glycerine 8.000
Sorbitol 2.000
Water q.s.
1 Available as Quadrol from BASF-Wyandotte 2 Available as Carbopol 941 from B.F. Goodrich Company
-18EXAMPLE IV
A facial cleansing composition for topical administration is prepared by combining the following ingredients:
Ingredients Percent w/w 5 Ν,Ν,Ν',N'-tetrakis(2-hydroxypropyl)ethylenedi amine monolaurylphosphate 3.000 Lauric acid 1.000 Potassium coco(hydrolysed animal protein) 0.500 Hydroxyethyl cellulose 2.000 10 Methyl paraben 0.100 Propyl paraben 0.100 Glycerin 3.000 Fragrance 0.100 Color 0.001 15 Water q.s. EXAMPLE V A facial cleansing gel composition for topical administratic prepared by combining the following Ingredients: Ingredients Percent w/w 20 Ν,Ν,Ν', Ν'-tetrakis(2-hydroxypropyl)ethylenediamine monolaurylphosphate 10.000 Acrylic acid polymer 0.500 Ν,Ν,Ν',N'-tetrakis(2-hydroxypropyl) ethylenediamine 1.000 25 Glycerin 5.000 Lauric acid 2.000 Water q.s.
EXAMPLE VI A facial shaving foam composition for topical administration prepared by combining the following ingredients: IngredWs Percent w/w 5 N,N,N',N'-tetraki s(2-hydroxypropyl) ethylenedi amine monolaurylphosphate Ν,Ν,Ν',N'-tetrakis(2-hydroxypropyl)- 7.000 ethylenediamine monopal mityl phosphate 7.000 Laurie acid 1.500 10 Palmityl acid Ν,Ν,Ν',N'-tetrakis(2-hydroxypropyl)- 1.500 ethylenediamine 1.500 Fragrance 0.100 Aloe Vera 2.000 15 Water q.s.
EXAMPLE VII A facial cleansing composition for topical administration 20 prepared by combining the following ingredients: Ingredients Ν,Ν,Ν',N'-tetrakis(2-hydroxypropyl)ethylenediamine (1 mole ethoxylated ) Percent w/w monolaurylphosphate 2.500 25 Butylene Glycol 2.500 Methylparaben 0.250 Propylparaben 0.150 Potassium coco(hydrolysed animal protein)1 0.032 Glycerin 2.000 30 Aloe Vera 0.500 Fragrance 0.050 Color 0.170 Xanthan gum2 0.050 Water q.s.
1 Available as Lamepon S from Henkel Corporation 2 Available as Keltrol T from Kelco Corporation
Claims (21)
1. A surfactant compound having low irritation effect to human skin of the formula: OX x R0--P--0X 2 II 5 0 wherein R is a hydrophobic group or the condensation product of a hydrophobic group with ethylene oxide, and wherein X x and X 2 are independently selected from the group consisting of hydrogen, alkali metal, ammonium, substituted ammonium and alkylene diamine, provided 10 that at least one of X x and X 2 is a totally hydroxyalkylated alkylene diamine.
2. A compound according to Claim 1 wherein R is alkyl or alkenyl having an average of from about 10 to about 18 carbon atoms and wherein said substituted ammonium is selected from the group consisting of alkoxylated ammonium, alkyl ammonium, alkoxylated aliphatic amines and 5 polyethoxylated amines.
3. A compound according to Claim 2 wherein R is alkyl or alkenyl having an average of from about 10 to 14 carbon atoms, and wherein said alkali metal is selected from the group consisting of sodium, potassium and lithium and mixtures thereof.
4. A compound according to Claim 3 wherein one of X x and X 2 is alkyl ammonium and said alkylammonium is selected from the group consisting of trimethyl ammonium, trlethylammonium, di butyl ammonium, butyldimethylammonium, Isopropyl dimethyl ammonium, diglycolamines, glucamines 5. And mixtures thereof and wherein said substituted alkylammonium is a hydroxyalkylammonium.
5. A compound according to Claim 4 wherein R is a condensation product of a hydrophobic group with from about 1 to about 10 moles of ethylene oxide. -216. A compound according to Claim 5 wherein at least one of X x and X 2 is a totally hydroxyalkylated alkylene diamine wherein the alkylene moiety contains from about 2 to about
6. Carbon atoms, said totally hydroxyalkylated alkylene diamine having been oxyalkylated with an 5 alkylene oxide containing at least about 2 carbon atoms or a mixture of alkylene oxides containing 2 or more carbon atoms.
7. A compound according to Claim 6 wherein at least one of X x and X 2 is Ν,Ν,Ν',N'-tetrakis(2-hydroxypropyl)ethylenediamine.
8. A detergent composition having low irritation effect comprising: (a) from about 1% to about 99% of one or more of a surfactant compound having the formula: 0X x 5 RO--P--OX 2 H wherein R 1s a hydrophobic group or the condensation product of a hydrophobic group with ethylene oxide, and wherein X x and X 2 are independently selected from the group consisting of hydro10 gen, alkali metal, ammonium, substituted ammonium and alkylene diamine, provided that at least one of X x and X 2 is an alkylene diamine; and (b) from about 99% to about 1% of a detergent carrier.
9. A detergent composition according to Claim 8 wherein R is alkyl or alkenyl having an average of from about 10 to about 18 carbon atoms and wherein said substituted ammonium is selected from the group consisting of alkoxylated ammonium, alkyl ammonium, alkoxylated 5 aliphatic amines and polyethoxylated amines.
10. A detergent composition according to Claim 9 wherein R is alkyl or alkenyl having an average of from about 10 to 14 carbon atoms and wherein said alkali metal is selected from the group consisting of sodium, potassium and lithium and mixtures thereof. -2211. A detergent composition according to Claim 10 wherein said alkylammonium is selected from the group consisting of trimethyl ammonium, triethyl ammonium, di butyl ammonium, butyl dimethyl ammonium, and isopropyl di methyl ammonium and mixtures thereof and wherein said sub5 stituted alkylammonium is a hydroxyalkylammonium.
11. 12. A detergent composition according to Claim 11 wherein at least one of X; and X 2 is a totally hydroxyalkylated alkylene diamine and wherein R is a condensation product of a hydrophobic group with from about 1 to about 10 moles of ethylene oxide.
12. 13. A detergent composition according to Claim 12 wherein at least one of X x and X 2 is a hydroxyalkylated alkylene diamine wherein the said alkylene contains from 2 to about 6 carbon atoms, said alkylene diamine having been oxyalkylated with an alkylene oxide containing at 5 least 2 carbon atoms or a mixture of alkylene oxides containing from 2 or more carbon atoms.
13. 14. A detergent composition according to Claim 13 wherein at least one of X x and X 2 is Ν,Ν,Ν',N'-tetrakis(2-hydroxypropyl)-ethylene-diamine.
14. 15. A detergent composition according to Claim 14 in a form selected from the group consisting of soaps, creams, solutions, mouthwashes, dentifrices or shampoos.
15. 16. A detergent composition according to Claim 8 comprising a mixture of the diamine monoalkyl phosphate salts wherein R is selected from the group consisting of C 12 to C 14 alkyl or alkenyl and C ie to C ie alkyl or alkenyl and wherein said salts are present in a ratio of from 5 about 60:40 to about 40:60.
16. 17. A detergent composition according to Claim 8 comprising a mixture of the diamine monoalkyl phosphate salts wherein R is selected from the group consisting of the condensation product of a C 12 to C 14 alkyl or alkenyl with from about 1 to about 10 moles of ethylene oxide and the 5 condensation product of a C ie to C ie alkyl or alkenyl with from about 1 to about 10 moles of ethylene oxide and wherein said salts are present in a ratio of from about 60:40 to about 40:60, respectively. -2318. A detergent composition having low irritation effect comprising: (a) one or more of a surfactant compound having the formula: 0X x RO--P--OX, u wherein R is a hydrophobic group or the condensation product of a hydrophobic group with ethylene oxide and wherein Xj and X 2 are independently selected from the group consisting of hydrogen, alkali metal, ammonium, substituted ammonium and alkylene diamine, provided that at least one of X 3 and X 2 is an alkylene diamine; and (b) one or more of a surfactant compound having the formula: OX j RO--P--OR u wherein R is a hydrophobic group or the condensation product of a hydrophobic group with ethylene oxide and wherein X 3 is selected from the group consisting of hydrogen, alkali metal, ammonium, substituted ammonium and alkylene diamine; wherein the ratio of (a) to (b) is from about 99:1 to about 70:30.
17. 19. A detergent composition according to Claim 18 wherein R is alkyl or alkenyl having an average of from about 10 to 18 carbon atoms or R is the condensation product of an alkyl or alkenyl having an average of from about 10 to 18 carbon atoms with from about 1 to about 10 moles of ethylene oxide, wherein said substituted ammonium is selected from the group consisting of alkoxylated ammonium, alkyl ammonium, alkoxylated aliphatic amines, polyethoxylated amines and wherein at least one of X x and X 2 is N,N,N',N'-tetrakis(2-hydroxypropyl)ethylene-d1amine.
18. 20. A detergent composition according to Claim 18 in a form selected from the group consisting of soaps, creams, solutions, mouthwashes, dentifrices or shampoos. -2421. A surfactant compound as claimed in Claim 1, substantially as hereinbefore described and exemplified.
19. 22. A process for the preparation of a surfactant compound as claimed in Claim 1, substantially as hereinbefore described and exemplified.
20. 23. A surfactant compound as claimed in Claim 1, whenever prepared by a process claimed in Claim 22.
21. 24. A detergent composition according to Claim 8 or 18, substantially as hereinbefore described and exemplified.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US50015190A | 1990-03-27 | 1990-03-27 | |
US64552091A | 1991-01-24 | 1991-01-24 |
Publications (1)
Publication Number | Publication Date |
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IE911002A1 true IE911002A1 (en) | 1991-10-09 |
Family
ID=27053427
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IE100291A IE911002A1 (en) | 1990-03-27 | 1991-03-26 | Novel surfactants and surfactant compositions |
Country Status (9)
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EP (1) | EP0521980A4 (en) |
JP (1) | JPH05506018A (en) |
CN (1) | CN1029912C (en) |
AU (1) | AU7581791A (en) |
CA (1) | CA2078442C (en) |
IE (1) | IE911002A1 (en) |
NZ (1) | NZ237587A (en) |
PT (1) | PT97096B (en) |
WO (1) | WO1991014693A1 (en) |
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US6221822B1 (en) | 1995-10-30 | 2001-04-24 | Tomah Products, Inc. | Detergent compositions having polyalkoxylated amine foam stabilizers |
US5719118A (en) * | 1995-10-30 | 1998-02-17 | Tomah Products, Inc. | Detergent compositions having polyalkoxylated amine foam stabilizers and method for cleaning including stabilized detergent foam |
DE19756373A1 (en) | 1997-12-18 | 1999-06-24 | Clariant Gmbh | alkyl phosphates |
CN102504615B (en) * | 2011-11-17 | 2013-08-07 | 中国科学院宁波材料技术与工程研究所 | Antibacterial agent preparation method for antibacterial plastic product |
JP5959932B2 (en) * | 2012-05-18 | 2016-08-02 | 株式会社ダイゾー | Foamable aerosol composition |
WO2019027999A1 (en) * | 2017-07-31 | 2019-02-07 | Ohio State Innovation Foundation | Biomimetic nanomaterials and uses thereof |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2758093A (en) * | 1948-06-22 | 1956-08-07 | Textilana Corp | Laundering compositions containing ortho-phosphoric acid esters |
US3442727A (en) * | 1967-08-03 | 1969-05-06 | Atlas Chem Ind | Emulsified nitric acid blasting composition and method of preparing same |
US3954648A (en) * | 1969-12-22 | 1976-05-04 | Pennwalt Corporation | Coatings removal composition containing an alkali metal hydroxide, an oxygenated organic solvent, and an amine |
JPS6035959B2 (en) * | 1977-06-30 | 1985-08-17 | 日本油脂株式会社 | Dispersed fuel manufacturing method |
US4290904A (en) * | 1980-12-01 | 1981-09-22 | Neutrogena Corporation | Transparent soap |
US4686058A (en) * | 1981-04-13 | 1987-08-11 | Basf Corporation | Thickened-water based hydraulic fluids |
JPS5874798A (en) * | 1981-10-28 | 1983-05-06 | 花王株式会社 | Shampoo composition |
-
1991
- 1991-03-11 JP JP91507206A patent/JPH05506018A/en active Pending
- 1991-03-11 CA CA 2078442 patent/CA2078442C/en not_active Expired - Fee Related
- 1991-03-11 EP EP19910906853 patent/EP0521980A4/en not_active Ceased
- 1991-03-11 WO PCT/US1991/001622 patent/WO1991014693A1/en not_active Application Discontinuation
- 1991-03-11 AU AU75817/91A patent/AU7581791A/en not_active Abandoned
- 1991-03-21 PT PT9709691A patent/PT97096B/en not_active IP Right Cessation
- 1991-03-26 NZ NZ23758791A patent/NZ237587A/en unknown
- 1991-03-26 IE IE100291A patent/IE911002A1/en unknown
- 1991-03-27 CN CN 91102024 patent/CN1029912C/en not_active Expired - Fee Related
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CA2078442A1 (en) | 1991-09-28 |
PT97096A (en) | 1991-12-31 |
CA2078442C (en) | 1995-12-05 |
AU7581791A (en) | 1991-10-21 |
PT97096B (en) | 1998-08-31 |
EP0521980A1 (en) | 1993-01-13 |
JPH05506018A (en) | 1993-09-02 |
WO1991014693A1 (en) | 1991-10-03 |
CN1029912C (en) | 1995-10-04 |
NZ237587A (en) | 1994-02-25 |
EP0521980A4 (en) | 1993-08-25 |
CN1055385A (en) | 1991-10-16 |
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