US3668136A - Compatible anionic-catonic surfactant compositions - Google Patents
Compatible anionic-catonic surfactant compositions Download PDFInfo
- Publication number
- US3668136A US3668136A US839698A US3668136DA US3668136A US 3668136 A US3668136 A US 3668136A US 839698 A US839698 A US 839698A US 3668136D A US3668136D A US 3668136DA US 3668136 A US3668136 A US 3668136A
- Authority
- US
- United States
- Prior art keywords
- alkyl
- fatty acid
- carbon atoms
- sulfonates
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 239000000203 mixture Substances 0.000 title claims abstract description 66
- 239000004094 surface-active agent Substances 0.000 title abstract description 11
- -1 polyoxypropylene groups Polymers 0.000 claims abstract description 142
- 239000003945 anionic surfactant Substances 0.000 claims abstract description 82
- 239000003093 cationic surfactant Substances 0.000 claims abstract description 78
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims abstract description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 153
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 83
- 229930195729 fatty acid Natural products 0.000 claims description 83
- 239000000194 fatty acid Substances 0.000 claims description 83
- 150000004665 fatty acids Chemical class 0.000 claims description 82
- 125000000217 alkyl group Chemical group 0.000 claims description 79
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 57
- 125000002091 cationic group Chemical group 0.000 claims description 35
- 229910019142 PO4 Inorganic materials 0.000 claims description 32
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 claims description 32
- 235000021317 phosphate Nutrition 0.000 claims description 32
- 150000003871 sulfonates Chemical class 0.000 claims description 31
- 239000000344 soap Substances 0.000 claims description 29
- 150000001408 amides Chemical class 0.000 claims description 28
- 150000008051 alkyl sulfates Chemical class 0.000 claims description 27
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 27
- 150000005846 sugar alcohols Polymers 0.000 claims description 27
- 150000001450 anions Chemical class 0.000 claims description 26
- 125000004185 ester group Chemical group 0.000 claims description 26
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 25
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 21
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 20
- 125000001475 halogen functional group Chemical group 0.000 claims description 18
- 125000003342 alkenyl group Chemical group 0.000 claims description 16
- 150000004996 alkyl benzenes Chemical class 0.000 claims description 13
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 8
- 229910052783 alkali metal Inorganic materials 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 229920001451 polypropylene glycol Polymers 0.000 claims description 7
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 6
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 claims description 4
- 229940077388 benzenesulfonate Drugs 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 239000006260 foam Substances 0.000 abstract description 17
- 230000003381 solubilizing effect Effects 0.000 abstract description 3
- 230000001747 exhibiting effect Effects 0.000 abstract description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 20
- 150000003254 radicals Chemical class 0.000 description 17
- 125000001453 quaternary ammonium group Chemical group 0.000 description 12
- 239000004215 Carbon black (E152) Substances 0.000 description 8
- 125000002947 alkylene group Chemical group 0.000 description 8
- 239000003599 detergent Substances 0.000 description 8
- 229930195733 hydrocarbon Natural products 0.000 description 8
- 229940117927 ethylene oxide Drugs 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 6
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 6
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 6
- 150000005194 ethylbenzenes Chemical class 0.000 description 6
- 150000005172 methylbenzenes Chemical class 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 5
- 125000005702 oxyalkylene group Chemical group 0.000 description 5
- 239000010452 phosphate Substances 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical class C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000012736 aqueous medium Substances 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 230000002209 hydrophobic effect Effects 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 159000000000 sodium salts Chemical class 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000008233 hard water Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- QABLOFMHHSOFRJ-UHFFFAOYSA-N methyl 2-chloroacetate Chemical compound COC(=O)CCl QABLOFMHHSOFRJ-UHFFFAOYSA-N 0.000 description 3
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 3
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 2
- ZPFAVCIQZKRBGF-UHFFFAOYSA-N 1,3,2-dioxathiolane 2,2-dioxide Chemical compound O=S1(=O)OCCO1 ZPFAVCIQZKRBGF-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 239000003240 coconut oil Substances 0.000 description 2
- 235000019864 coconut oil Nutrition 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 229960003750 ethyl chloride Drugs 0.000 description 2
- KSCHLNBLIAOANF-UHFFFAOYSA-M ethyl-hexadecyl-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CC KSCHLNBLIAOANF-UHFFFAOYSA-M 0.000 description 2
- LIWAQLJGPBVORC-UHFFFAOYSA-N ethylmethylamine Chemical compound CCNC LIWAQLJGPBVORC-UHFFFAOYSA-N 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- ACGUYXCXAPNIKK-UHFFFAOYSA-N hexachlorophene Chemical compound OC1=C(Cl)C=C(Cl)C(Cl)=C1CC1=C(O)C(Cl)=CC(Cl)=C1Cl ACGUYXCXAPNIKK-UHFFFAOYSA-N 0.000 description 2
- 229960004068 hexachlorophene Drugs 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000001165 hydrophobic group Chemical group 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 150000002924 oxiranes Chemical class 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- 239000002453 shampoo Substances 0.000 description 2
- 230000007928 solubilization Effects 0.000 description 2
- 238000005063 solubilization Methods 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 150000003460 sulfonic acids Chemical class 0.000 description 2
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 1
- ZFPGARUNNKGOBB-UHFFFAOYSA-N 1-Ethyl-2-pyrrolidinone Chemical compound CCN1CCCC1=O ZFPGARUNNKGOBB-UHFFFAOYSA-N 0.000 description 1
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical class C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 1
- AVFZOVWCLRSYKC-UHFFFAOYSA-N 1-methylpyrrolidine Chemical compound CN1CCCC1 AVFZOVWCLRSYKC-UHFFFAOYSA-N 0.000 description 1
- PMPBFICDXLLSRM-UHFFFAOYSA-N 1-propan-2-ylnaphthalene Chemical compound C1=CC=C2C(C(C)C)=CC=CC2=C1 PMPBFICDXLLSRM-UHFFFAOYSA-N 0.000 description 1
- KXIXHISTUVHOCY-UHFFFAOYSA-N 1-propan-2-ylpiperidine Chemical compound CC(C)N1CCCCC1 KXIXHISTUVHOCY-UHFFFAOYSA-N 0.000 description 1
- GHELJWBGTIKZQW-UHFFFAOYSA-N 1-propan-2-ylpyrrolidin-2-one Chemical compound CC(C)N1CCCC1=O GHELJWBGTIKZQW-UHFFFAOYSA-N 0.000 description 1
- WHNBDXQTMPYBAT-UHFFFAOYSA-N 2-butyloxirane Chemical compound CCCCC1CO1 WHNBDXQTMPYBAT-UHFFFAOYSA-N 0.000 description 1
- MNNZINNZIQVULG-UHFFFAOYSA-N 2-chloroethylbenzene Chemical compound ClCCC1=CC=CC=C1 MNNZINNZIQVULG-UHFFFAOYSA-N 0.000 description 1
- KPJKMUJJFXZGAX-UHFFFAOYSA-N 2-chloropropan-2-ylbenzene Chemical compound CC(C)(Cl)C1=CC=CC=C1 KPJKMUJJFXZGAX-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- SYURNNNQIFDVCA-UHFFFAOYSA-N 2-propyloxirane Chemical compound CCCC1CO1 SYURNNNQIFDVCA-UHFFFAOYSA-N 0.000 description 1
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical class OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- VKEQBMCRQDSRET-UHFFFAOYSA-N Methylone Chemical compound CNC(C)C(=O)C1=CC=C2OCOC2=C1 VKEQBMCRQDSRET-UHFFFAOYSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- HTLZVHNRZJPSMI-UHFFFAOYSA-N N-ethylpiperidine Chemical compound CCN1CCCCC1 HTLZVHNRZJPSMI-UHFFFAOYSA-N 0.000 description 1
- AHVYPIQETPWLSZ-UHFFFAOYSA-N N-methyl-pyrrolidine Natural products CN1CC=CC1 AHVYPIQETPWLSZ-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical class CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- 150000005524 benzylchlorides Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 239000012972 dimethylethanolamine Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 150000002193 fatty amides Chemical class 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 239000005414 inactive ingredient Substances 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005649 metathesis reaction Methods 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-N methyl sulfate Chemical compound COS(O)(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 230000015227 regulation of liquid surface tension Effects 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- JHJUUEHSAZXEEO-UHFFFAOYSA-M sodium;4-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=C(S([O-])(=O)=O)C=C1 JHJUUEHSAZXEEO-UHFFFAOYSA-M 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000003470 sulfuric acid monoesters Chemical class 0.000 description 1
- 239000003784 tall oil Substances 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
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
- C11D10/047—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap based on cationic surface-active compounds and soap
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/463—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/55—Phosphorus compounds
- A61K8/556—Derivatives containing from 2 to 10 oxyalkylene groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/86—Polyethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
-
- 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
- C11D1/38—Cationic compounds
- C11D1/65—Mixtures of anionic with cationic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/596—Mixtures of surface active compounds
-
- 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
- C11D1/04—Carboxylic acids or salts thereof
-
- 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
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
-
- 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
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
-
- 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
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium compounds
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
- Y10S516/03—Organic sulfoxy compound containing
- Y10S516/05—Organic amine, amide, or n-base containing
Definitions
- This invention relates to novel compositions of matter com prising mixtures of cationic surfactants of specific structure and anionic surfactants generally, the compositions having unique surface active properties in aqueous solution. More specifically this invention relates to mutually compatible mixtures of anionic surfactants and cationic detergents comprising quaternary ammonium compounds having a polyoxyalkylene group linked to the nitrogen.
- anionic surfactants or detergents which are disclosed in said patent as possessing the foregoing compatibility with said cationic surfactants are mono-alkali metal salts of polybasic carboxylic acid mono-esters of the terminal alkylol group of a poly-oxyalkylated organic compound containing a hydrophobic hydrocarbon radical on the opposite end of the poly-oxyalkylene chain which contains from about two to 20 oxyalkylene units having from two to three carbon atoms per unit, the said hydrophobic hydrocarbon radical containing from eight to about 21 carbon atoms.
- cationic surfactants having a quaternary ammonium radical and a hydrophobic hydrocarbon group as, for instance, cetyldimethylethylammonium chloride, or other cationic surfactants disclosed in the aforesaid U.S. Pat. No.
- 3,345,300 are admixed with numerous other anionic surfactants or detergents, such as, and particularly, those of the sulfate, sulfonate and phosphate ester types, such as sodium lauryl sulfate, sodium salts of sulfated higher fatty acid monoglycerides, dodecylbenzene sodium sulfonate, and sodium salts of phosphate esters of ethoxylated long chain alcohols and sodium salts of phosphate esters of ethoxylated long chain alkylphenols, incompatibility occurs in aqueous media and surfactant activity is effectively destroyed, precipitation usually occurring.
- column 10 last two lines, and column 11, lines 18 of said U.S. Pat. No. 3,345,300. See, also, U.S. Pat. No. 2,213,477.
- compositions are characterized by excellent compatibility in aqueous media and improved surface active characteristics, particularly with regard to foam boosting and stabilization, viscosity and solubilization in high-solid compositions.
- novel cationic surfactant-anionic surfactant compositions are especially suitable for use in cosmetic detergent formulations such as shampoos, body detergents, facial cleansers, bubble baths and the like because of the foam boosting and stabilization effect and the solubilization of germicidal ingredients such as hexachlorophene without the need for addition of inactive ingredients such as ethylene glycols or propylene glycols which are generally used for such purposes.
- the particular types of cationic surfactants which are utilized offer a distinct ad vantage over the commonly employed fatty amide and alkanolamide foam boosters and stabilizers which tend to build up viscosity, whereas said cationic surfactants function, in
- viscosity reducing agents thus offering, in the compositions of this invention, the highly desirable feature of simultaneously building foam and reducing viscosity.
- cationic quaternary ammonium compounds disclosed in the aforesaid U.S. Pats. Nos. 3,123,640; 3,123,641; 3,141,905 and 3,155,591, are represented by the formula wherein R is an alkyl radical containing from one to three carbon atoms, and more particularly from one to two carbon atoms, R, is an alkyl radical containing from one to three carbon atoms, and compounds wherein R and R, are joined together to form with the N atom a member of the group consisting of piperidine, methyl piperidine and pyrrolidine;
- R is an alkyl radical containing from one to four carbon atoms, n is a number up to and including 60, the total number of carbon atoms in R being at least 18; R is a member selected from the group consisting of 1) alkyl and alkenyl radicals containing not more than four carbon atoms, and (2) benzene; methyl benzenes; ethyl benzenes;
- R may comprise other radicals over and above those identified above, as, for instance, isopropyl benzene, naphthalene, methyl naphthalenes and isopropyl naphthalene.
- R may be a radical of a cyclic amine containing not more than six carbon atoms
- R is a polyoxyalkylene radical containing at least 18 carbon atoms and derived from an a-epoxide containing at least three carbon atoms, especially propyleneoxide.
- R is derived from propyleneoxide
- R is derived from a-epoxides containing more than three carbon atoms, a lesser number of such oxyalkylene groups can be present, subject to the limitation of R, containing at least 1 8 atoms.
- R is advantageously a lower alkyl or alkenyl radical containing from one to four carbon atoms; or a lower aliphatic-aryl radical containing seven to nine carbon atoms, notably an alkaryl radical; and A is an anion, it being important that the R radial, where it is alkyl, contain not more than three carbon atoms and especially that it contain from one to two carbon atoms and, hence, that it be methyl or ethyl; that, except where is derived from a cyclic amine, as hereafter pointed out, the R, radical does not contain over three carbon atoms, and, in any event, that the maximum number of carbon atoms in R and R, does not exceed a total of four or five; and that, while R may contain a minimum of six of the aforesaid oxyalkylene, particularly oxypropylene groups, and may contain 40, 50 or 60 or even 100 or more of said groups, the minimum number of said groups be eight, with the preferred range being 8 to 25
- R is where R is an alkyl radical containing from one to four carbon atoms, n and n are numbers the sum of which preferably does not exceed 60, the total number of carbon atoms in R, and R being at least 18; R is a hydrocarbon radical selected from the group consisting of alkyl and alkenyl radicals containing not more than four carbon atoms, or a lower aliphaticaromatic hydrocarbon radical containing from seven to nine carbon atoms; and A is an anion.
- R is an alkyl radical containing from one to three, and especially from one to two carbon atoms
- R is an alkyl radical containing from one to three carbon atoms
- alkylene contains not more than three carbon atoms
- R. is an alkyl radical containing from one to four carbon atoms, n is a number up to and preferably not exceeding 60, the total number of carbon atoms in R being at least 18;
- R is a hydrocarbon radical selected from the group consisting of alkyl and alkenyl radicals containing not more than four carbon atoms, or a lower aliphatic-aromatic hydrocarbon radical containing from seven to nine carbon atoms; and
- A is an anion.
- R,-O-alkyleneN where alkylene contains not more than 3 carbon atoms, RO is in which R4 is an alkyl radical containing from one to four carbon atoms, n, n and nare numbers the sum of which preferably does not exceed 60, the total number of carbon atoms in R, R, and R being at least 18; R is a hydrocarbon radical selected from the group consisting of alkyl and alkenyl radicals containing not more than four carbon atoms, or a lower aliphaticaromatic hydrocarbon radical containing from seven to nine carbon atoms; and A is an anion.
- quaternary ammonium type compounds having utility in the present invention fall into the category of or correspond to reaction products of quaternizing esters having a hydrocarbon alkyl or alkenyl radical containing not more than four carbon atoms, or a benzyl radical or a dimethylbenzyl radical or a lower alkylsubstituted or' chloror nitro-substituted benzyl radical, and an anion, with adducts of (a) aliphatic amines or cyclic amines containing a reactive hydrogen and a total of not more than six carbon atoms and in which no single aliphatic radical contains more than three carbon atoms, with (b) an a-epoxide containing at least three and advantageously from three to eight carbon atoms, the molal ratio of (a) to (b) being 1 of (a) to at least 6 of (b) when said a-epoxide contains three carbon atoms and ranging down to at least 2.5 of (
- R is an alkyl radical containing from one to three carbon atoms
- R is an alkyl radical containing from one to three carbon atoms or is the same as R
- R is a polyoxyalkylene radical containing at least 18 carbon atoms and derived from an a-epoxide containing from three to eight carbon atoms
- R is a hydroxy-alkyl radical containing from two to four carbon atoms
- A is hydroxyl or other anion.
- Such compounds are readily :produced by reacting the adducts, such as those described in Examples a to v of US. Pat. No.
- quaternary ammonium compounds which are particularly useful are reaction products of quaternizing esters in the form of alkyl and alkenyl halides, sulfates and sulfonates containing from one to four carbon atoms, exemplified by methyl chloride, ethyl chloride, methyl chloracetate, and one and two carbon atom alkyl sulfates; or aromatic quaternizing esters in the form of halides, sulfates and sulfonates advantageously containing from seven to nine carbon atoms, exemplified by benzyl chlorides, dimethylbenzyl chloride, and phenylethyl chloride, with adducts of (0) alkyl amines having
- the oxyalkylene groups substituted on the quaternary ammonium type compounds be derived from an a-epoxide containing at least three carbon atoms.
- the most important embodiment of the a-epoxide whose use is contemplated herein in the production of the desired quaternary ammonium type compounds is propyleneoxide
- the a epoxides containing four, five, six or more carbon atoms can be used but, for general reasons of lack of economy or commercial availability, are not preferred.
- a-epoxides Typical of such latter a-epoxides are butyleneoxides such as l,2-butyleneoxide, pentylene epoxides, hexylene epoxides, heptylene epoxides, octylene epoxides, dodecylene epoxides, and C C, olefin oxides or epoxides, and, as well, styrene epoxide. It will be seen that most of those of the a-epoxides in which the vicinal carbons are terminal can conveniently by represented by the formula where R is an alkyl radical.
- R is CH and in the representation of the group of propyleneoxide, butyleneoxides, pentyleneoxide and hexyleneoxide R contains from one to four carbon atoms. In the higher molecular weight alkylene oxides, R may contain as high as 16 carbon atoms.
- ethylene oxide cannot be employed as the sole alkylene oxide in preparing the quaternary ammonium cationic surfactants useful in preparing the novel anionic-cationic surfactant compositions of the present invention
- minor proportions thereof, not to exceed about 20 percent by weight of the propylene oxide, or other a-epoxide employed, can be utilized as hereafter described.
- Mixtures of two or more of the a-epoxides containing at least three carbon atoms can, of course, be used as such, as well as in conjunction with ethylene oxide, subject to the limitation that the ethylene oxide must not exceed the aforesaid 20 percent of the weight of said a-epoxides.
- the radical A can be any negative or salt-forming radical as, for instance, halogen such as chlorine, bromine and iodine; hydroxy; sulfate, alkyl-sulfuric acid such as methyl sulfuric acid or ethyl sulfuric acid (methosulfate of ethosulfate); nitrate; phosphate; acetate; formate; carbonate; lower alkyl (one to four carbon atoms) sulfonic acids; and the like.
- halogen such as chlorine, bromine and iodine
- hydroxy sulfate, alkyl-sulfuric acid such as methyl sulfuric acid or ethyl sulfuric acid (methosulfate of ethosulfate); nitrate; phosphate; acetate; formate; carbonate; lower alkyl (one to four carbon atoms) sulfonic acids; and the like.
- quaternary ammonium type compounds in which the anion is chlorine, bromine,
- the anionic surfactants which are compatible with the aforesaid quaternary ammonium compounds described herein, which mixtures form the novel compositions of the present invention, comprise a broad spectrum of compounds, as is well known to those skilled in the art.
- Members of this classification comprise the water-soluble salts such as the alkali metal and amine soaps of straight and branched chain fatty acids, said fatty acids being both naturally occurring, such as from coconut oil or from tall oil, and synthetically produced such as by paraffin oxidation; the water soluble salts of organic sulfonic acids, alkyl sulfuric acids and sulfuric acid esters of polyhydric alcohols incompletely esterified with a fatty acid of high molecular weight, sulfated and sulfonated higher fatty acid amides and alkanolamides which include the sulfated fatty oil, sulfated fatty acids, sulfated straight chain and branched chain C -C alcohols, sulfated alkyl
- alkyl sulfates prepared by reacting a fatty alcohol with sulfuric acid or chlorosulfonic acid, said fatty alcohol having from about eight to 18 carbon atoms, of particular utility in preparing the compositions of the present invention being the alkali metal, alkaline earth metal, ammonium, lower amine and a1- kanolamine alkyl sulfates wherein the alkyl group contains from eight to 18 carbon atoms.
- alkanesulfonates such as the di-alkyl sulfo-succinates, amide linked sulfonates and various derivatives thereof.
- alkylaryl sulfonates both straight and branched chain, sodium dodecylbenzene sulfonate being the common commercial product.
- alkylaryl sulfonates usually contain from about six to 26 carbon atoms in the alkyl chain.
- alkylaryl sulfonates may also contain intermediate linkages such as amide and hydrazide linkages, as exemplified by the sulfonated a-alkylbenzimidazoles, and ester and ether linkages.
- intermediate linkages such as amide and hydrazide linkages, as exemplified by the sulfonated a-alkylbenzimidazoles, and ester and ether linkages.
- suitable anionic surfactants are the esters of the oxy acids of phosphorous with aliphatic alcohols having from about six to 18 carbon atoms and alkyl phenols wherein the alkyl chain contains from eight to 18 carbon atoms.
- anionic detergents wherein the anionic surfactant solubilizing group is a member selected from the group consisting of SO H, SO H, COOH and the water-soluble salts thereof especially the alkali metal, alkaline earth metal, ammonium and lower amine and alkanolamine salts.
- anionic surfactants are disclosed in numerous patents among which may be mentioned, by way of illustration, U.S. Pat. Nos. 2,383,737; 2,486,921; 2,920,045; and 3,004,056.
- the aforesaid quaternary ammonium surfactant may be combined with the aforesaid anionic surfactants over a wide range of proportions, since the compatibility is not limited by any critical weight proportions, and there will be no significant diminution of surface active properties, no matter what the ratio of the said surfactants may be to each other.
- the aforesaid quaternary ammonium surfactant there is employed from about 20 to 40 percent, better still about 25 to 30 percent, of said quaternary ammonium surfactant, based on the weight of combined cationic and anionic surfactants in the compositions.
- EXAMPLE 1 The following tabulated data represent the results of the Shake Foam Test (50 mls total liquid in 250 ml cylinder, 20 inversions).
- the anionic surfactant employed was sodium lauryl sulfate; the cationic surfactant was a quaternary ammonium compound of the formula Cg: Cal-I /1 CH3 R Cl but a cationic surfactant similar to that in Example 1 was employed except the polyoxypropylene radical contained about 30 oxypropylene groups.
- EXAMPLE 3 The shake foa'm test was repeated with the cationic surfac- 40 tant of Example 1 and the triethanolamine salt of dodecylbenzene sulfonic acid as the anionic surfactant.
- compositions made in accordance with the present invention are as follows, the pro portions stated being in weight percent.
- EXAMPLE 6 Phosphate ester of [0 mol ethylene oxide adduct of nonyl phenol (sodium salt) 25 mol propylene oxide adduct of dimethylamine quaternized with ethyl chloride
- EXAMPLE 7 Phosphate ester of 12 mol ethylene oxide adduct of dodecyl alcohol (triethanolamine salt) 16 mol propylene oxide adduct of methylethylamine quaternized with benzyl chloride
- EXAMPLE 8 Why acid monoester of sulfuric acid monoester of glycerol (triethanolamine salt) 18 mol propylene oxide adduct of dimethylethanolamine quatemized with methyl chloracetate
- EXAMPLE 9 Sodium lauryl sulfate 70% 12 mol butylene oxide adduct of dimethylamine quaternized with dimethyl sulfate wherein R is alkyl containing from one to three carbon atoms, R, is
- composition according to claim 1 wherein the anionic surfactant is selected from the group consisting of alkyl sulfates, alkylaryl sulfonates and fatty carboxylic acid soaps 3.
- the anionic surfactant is an alkali metal alkyl sulfate wherein the alkyl group contains from eight to 18 carbon atoms.
- composition according to claim 2 wherein the anionic surfactant is an alkali metal alkyl benzene sulfonate wherein the alkyl group contains from eight to 18 carbon atoms.
- composition according to claim 1 in which the R radical of said cationic surfactant compound contains a polyoxyethylene radical in which the ethylene oxide constitutes not more than 20 percent by weight of said R radical.
- R is alkyl containing from one to four carbon atoms, n and n are numbers the sum of which does not exceed 60, the total number of carbon atoms in R, and R being at least 18;
- R is a member selected from the group consisting of l alkyl and alkenyl containing not more than four carbon atoms, and (2)benzene; methyl benzenes', ethyl benzenes;
- A is an innocuous anion.
- a composition consisting essentially of a water-soluble I anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, etherand amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is alkyl containing from one to three carbon atoms, alkylene contains not more than three carbon atoms, R,-0 is and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo and mono-nitro nuclearly substitute
- a composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, etherand amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on theweight of combined cationic and anionic surfactants, corresponding to the formula where alkylene contains not more than three carbon atoms,
- R is alkyl containing from one to four carbon atoms, n, n and n are numbers the sum of which does not exceed 60, the total number of carbon atoms in R, R and R being at least 18;
- R is a member selected from the group consisting of 1) alkyl and alkenyl containing not more than four carbon atoms, and (2)benzene; methyl benzenes; ethyl benzenes;
- A is an innocuous anion.
- atoms is R; being at least 18, v is a number at least 1 with the proviso that the weight ratio of (C Ht0-), to R is not greater than one to four,
- X is a member selected from the group consisting of (l alkyl and alkenyl containing from one to four carbon atoms, and (2) benzene; lower alkyl benzenes in which the lower alkyl contain from one to four carbon and their methyl and ethyl nuclearly substituted derivatives;
- R is alkyl containing from one to four carbon atoms
- n is a number up to and including 60, the total number of carbon atoms in R being at least 18
- v is a number at least 1 with the proviso that the weight ratio of (C H -O-),. to R is not greater than one to four
- X is a member selected from the group consisting of l alkyl and alkenyl containing from one to four carbon atoms, and benzene; lower alkyl benzenes in which the lower alkyls contain from one to four carbon atoms,
- a composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, etherand amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is an alkyl containing from one to three carbon atoms R is greater than one to four, X is a member selected from the group consisting of 1) alkyl and alkenyl containing from one to four carbon atoms, and (2) benzene;
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Abstract
Novel surfactant compositions comprising an anionic surfactant and certain cationic surfactants compatible with same and in the form of quaternary ammonium compounds containing polyoxypropylene groups, said compositions exhibiting imprsved foam and solubilizing characteristics.
Description
O United States Patent 1151 3,668,136 Barker June 6, 1972 1541 COMPATIBLE ANIONIC-CATONIC 3,141,905 7/1964 Longley ..260/567.6 SURFACTANT COMPOSITIONS 3,155,591 11/1964 Hilfer 424/70 3,325,414 6/1967 lnamorato .....252/137 [72] Bark", Lawn- 3,345,300 10/1967 Speel ..252/547 [73] Assignee: Witco Chemical Corporation, New York,
FOREIGN PATENTS OR APPLICATIONS [22] Filed: July 7, 1969 873,214 7/1961 Great Britain 252/8.75 [21] Appl. No.: 839,698
Primary Examiner-Leon D. Rosdol 52 U.S. c1 ..252/117, 252/355, 252/528,
H 2 7 Attorney-Wallenstcin, Spangenbcrg, Hattis and Strampel [51] .Int.Cl. ..C11d9/46,C11d1/65 [58] Field ofSearch ..252 117, 152, 355 ABSTRACT Novel surfactant compositions comprising an anionic surfac- [56] Rderences Cited tant and certain cationic surfactants compatible with same UNITED STATES PATENTS and in the form of quaternary ammonium compounds containing polyoxypropylene groups, said compositions exhibiting 2,734,830 ,2/1956 Hagge et a1. ,.l 17/47 imprsved f and Solubilizing h i fi 3,123,640 3/1964 Langley ..260/567.6 3,123,641 3/1964 Longley ..260/567.6 20 Claims, N0 Drawings COMPATIBLE ANlONlC-CATONIC SURFACTANT COMPOSITIONS This invention relates to novel compositions of matter com prising mixtures of cationic surfactants of specific structure and anionic surfactants generally, the compositions having unique surface active properties in aqueous solution. More specifically this invention relates to mutually compatible mixtures of anionic surfactants and cationic detergents comprising quaternary ammonium compounds having a polyoxyalkylene group linked to the nitrogen.
It is well known in the art that, generally speaking, cationic and anionic surfactants are incompatible in the same solution, both the cationic and anionic ingredients losing their surface active properties by virtue of interaction between the negatively charged hydrophobic group of the anionic surfactant and the positively charged hydrophobic group of cationic surfactant. The usual effect of such interaction is the elimination of the surface active properties of both materials.
It has, however, heretofore been known, as shown in U.S. Pat. No. 3,345,300, to admix cationic surfactants having a quaternary ammonium radical and a hydrophobic hydrocarbon group as, for instance, cetyldimethylethylammonium chloride, with certain specific types of anionic surfactants or detergents to produce compositions which, when added to water or aqueous media, are mutually compatible and do not interact to render their surfactant or detergent properties ineffectual. The specific types of anionic surfactants or detergents which are disclosed in said patent as possessing the foregoing compatibility with said cationic surfactants are mono-alkali metal salts of polybasic carboxylic acid mono-esters of the terminal alkylol group of a poly-oxyalkylated organic compound containing a hydrophobic hydrocarbon radical on the opposite end of the poly-oxyalkylene chain which contains from about two to 20 oxyalkylene units having from two to three carbon atoms per unit, the said hydrophobic hydrocarbon radical containing from eight to about 21 carbon atoms.
When cationic surfactants having a quaternary ammonium radical and a hydrophobic hydrocarbon group, as, for instance, cetyldimethylethylammonium chloride, or other cationic surfactants disclosed in the aforesaid U.S. Pat. No. 3,345,300, are admixed with numerous other anionic surfactants or detergents, such as, and particularly, those of the sulfate, sulfonate and phosphate ester types, such as sodium lauryl sulfate, sodium salts of sulfated higher fatty acid monoglycerides, dodecylbenzene sodium sulfonate, and sodium salts of phosphate esters of ethoxylated long chain alcohols and sodium salts of phosphate esters of ethoxylated long chain alkylphenols, incompatibility occurs in aqueous media and surfactant activity is effectively destroyed, precipitation usually occurring. Note, for instance, column 10, last two lines, and column 11, lines 18 of said U.S. Pat. No. 3,345,300. See, also, U.S. Pat. No. 2,213,477.
It has been discovered, suprisingly, that when certain particular types of cationic surfactants, hereafter described in detail, are admixed with anionic surfactants generally, and particularly where the anionic surfactants are of the sulfate, sulfonate and phosphate ester types, the resulting compositions are characterized by excellent compatibility in aqueous media and improved surface active characteristics, particularly with regard to foam boosting and stabilization, viscosity and solubilization in high-solid compositions. These novel cationic surfactant-anionic surfactant compositions are especially suitable for use in cosmetic detergent formulations such as shampoos, body detergents, facial cleansers, bubble baths and the like because of the foam boosting and stabilization effect and the solubilization of germicidal ingredients such as hexachlorophene without the need for addition of inactive ingredients such as ethylene glycols or propylene glycols which are generally used for such purposes. In addition, in the novel compositions of the present invention, the particular types of cationic surfactants which are utilized offer a distinct ad vantage over the commonly employed fatty amide and alkanolamide foam boosters and stabilizers which tend to build up viscosity, whereas said cationic surfactants function, in
among other ways, as viscosity reducing agents, thus offering, in the compositions of this invention, the highly desirable feature of simultaneously building foam and reducing viscosity.
The particular types of cationic surfactants which have been discovered to be useful in the compositions of the present invention are shown in U.S. Pat. Nos. 3,123,640; 3,123,641; 3,141,905 and 3,155,591, the disclosures of which patents in relation to said cationic surfactants are herewith incorporated into the present specification by reference.
Various of the cationic quaternary ammonium compounds, disclosed in the aforesaid U.S. Pats. Nos. 3,123,640; 3,123,641; 3,141,905 and 3,155,591, are represented by the formula wherein R is an alkyl radical containing from one to three carbon atoms, and more particularly from one to two carbon atoms, R, is an alkyl radical containing from one to three carbon atoms, and compounds wherein R and R, are joined together to form with the N atom a member of the group consisting of piperidine, methyl piperidine and pyrrolidine;
where R, is an alkyl radical containing from one to four carbon atoms, n is a number up to and including 60, the total number of carbon atoms in R being at least 18; R is a member selected from the group consisting of 1) alkyl and alkenyl radicals containing not more than four carbon atoms, and (2) benzene; methyl benzenes; ethyl benzenes;
and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo and mononitro nuclearly substituted derivatives of the foregoing; and A is an innocuous anion. It may be noted that, in the above formula, in place of piperidine, methyl piperidine and pyrrolidine, other heterocyclic compounds can be used in which the R and R, radicals are joined together with the N atom, as, for instance, ethyl piperidine, isopropyl piperidine, methyl pyrrolidine, ethyl pyrrolidone, isopropyl pyrrolidone, and indole. Similarly, R may comprise other radicals over and above those identified above, as, for instance, isopropyl benzene, naphthalene, methyl naphthalenes and isopropyl naphthalene.
Again, as disclosed in the aforesaid patents showing the particular types of quaternary ammonium compounds which, according to the present invention, have been found to possess utility for the purposes of this invention, there are those derived from low molecular weight alkyl secondary amines and cyclic amines which can be represented by the formula wherein R is an alkyl radical containing from one to three and more particularly from one to two carbon atoms, R, is an alkyl radical containing from one to three carbon atoms, or
may be a radical of a cyclic amine containing not more than six carbon atoms, R is a polyoxyalkylene radical containing at least 18 carbon atoms and derived from an a-epoxide containing at least three carbon atoms, especially propyleneoxide. In those cases where R is derived from propyleneoxide, there will be at least six of such propyleneoxide groups in R and, more particularly, it is desirable that R contain from 8 to 30 oxypropylene groups. Where R is derived from a-epoxides containing more than three carbon atoms, a lesser number of such oxyalkylene groups can be present, subject to the limitation of R, containing at least 1 8 atoms. R; is advantageously a lower alkyl or alkenyl radical containing from one to four carbon atoms; or a lower aliphatic-aryl radical containing seven to nine carbon atoms, notably an alkaryl radical; and A is an anion, it being important that the R radial, where it is alkyl, contain not more than three carbon atoms and especially that it contain from one to two carbon atoms and, hence, that it be methyl or ethyl; that, except where is derived from a cyclic amine, as hereafter pointed out, the R, radical does not contain over three carbon atoms, and, in any event, that the maximum number of carbon atoms in R and R, does not exceed a total of four or five; and that, while R may contain a minimum of six of the aforesaid oxyalkylene, particularly oxypropylene groups, and may contain 40, 50 or 60 or even 100 or more of said groups, the minimum number of said groups be eight, with the preferred range being 8 to 25 or 30 of said groups, and an n being advantageously from 6 to 30 where the polyoxyalkylene radical is a polyoxypropylene radical.
As shown in U.S. Pat. No. 3,123,641, at least most of those of the particularly preferred quarternary ammonium type compounds which are derived from lower mono-alkyl amines can be represented by the formula (II) Re where R is an alkyl radical containing from one to three, and especially from one to two, carbon atoms, R, is
and R is where R is an alkyl radical containing from one to four carbon atoms, n and n are numbers the sum of which preferably does not exceed 60, the total number of carbon atoms in R, and R being at least 18; R is a hydrocarbon radical selected from the group consisting of alkyl and alkenyl radicals containing not more than four carbon atoms, or a lower aliphaticaromatic hydrocarbon radical containing from seven to nine carbon atoms; and A is an anion.
Various of those particularly preferred quaternary ammonium type compounds employed in the invention which are derived from lower dialkyl monoalkanolamines can be represented by the formula where R is an alkyl radical containing from one to three, and especially from one to two carbon atoms; R, is an alkyl radical containing from one to three carbon atoms; alkylene contains not more than three carbon atoms, R,-
is where R., is an alkyl radical containing from one to four carbon atoms, n is a number up to and preferably not exceeding 60, the total number of carbon atoms in R being at least 18; R is a hydrocarbon radical selected from the group consisting of alkyl and alkenyl radicals containing not more than four carbon atoms, or a lower aliphatic-aromatic hydrocarbon radical containing from seven to nine carbon atoms; and A is an anion.
Again, various of those of the particularly preferred quaternary ammonium type compounds used in the compositions of the present invention which are derived from lower monoalkyl dialkanolamines can be represented by the formula IV s Rg-O-alkylene A where R is an alkyl radical containing from one to three, and especially from one to two, carbon atoms, alkylene contains not more than three carbon atoms, R,0 is
andR is (V) R-O-alkylcne Ra R2 A and (VI) RO-alkylenc\ R;
R,-O-alkyleneN where alkylene contains not more than 3 carbon atoms, RO is in which R4 is an alkyl radical containing from one to four carbon atoms, n, n and nare numbers the sum of which preferably does not exceed 60, the total number of carbon atoms in R, R, and R being at least 18; R is a hydrocarbon radical selected from the group consisting of alkyl and alkenyl radicals containing not more than four carbon atoms, or a lower aliphaticaromatic hydrocarbon radical containing from seven to nine carbon atoms; and A is an anion.
Most of the quaternary ammonium type compounds having utility in the present invention fall into the category of or correspond to reaction products of quaternizing esters having a hydrocarbon alkyl or alkenyl radical containing not more than four carbon atoms, or a benzyl radical or a dimethylbenzyl radical or a lower alkylsubstituted or' chloror nitro-substituted benzyl radical, and an anion, with adducts of (a) aliphatic amines or cyclic amines containing a reactive hydrogen and a total of not more than six carbon atoms and in which no single aliphatic radical contains more than three carbon atoms, with (b) an a-epoxide containing at least three and advantageously from three to eight carbon atoms, the molal ratio of (a) to (b) being 1 of (a) to at least 6 of (b) when said a-epoxide contains three carbon atoms and ranging down to at least 2.5 of (b) when said a-epoxide contains eight carbon atoms.
Still others of the quaternary ammonium compounds that may be employed in the compositions of this invention can be represented by the formula Where R is an alkyl radical containing from one to three carbon atoms, R is an alkyl radical containing from one to three carbon atoms or is the same as R R is a polyoxyalkylene radical containing at least 18 carbon atoms and derived from an a-epoxide containing from three to eight carbon atoms, R is a hydroxy-alkyl radical containing from two to four carbon atoms and A is hydroxyl or other anion. Such compounds are readily :produced by reacting the adducts, such as those described in Examples a to v of US. Pat. No. 3,123,641, with ethyleneoxide in an aqueous medium in accordance with known quaternizing techniques. Typical of such compounds are those corresponding to the formulae where R is a polyoxypropylene or polyoxybutylene radical containing say from 6 to 30 oxypropylene or oxybutylene groups.
While, as indicated, many of the quaternary ammonium type compounds having utility for the purposes of this invention can be represented by the above formulae, they may, in general, best be described in the form of reaction products of identified ingredients, as hereafter pointed out. Thus, for example, quaternary ammonium compounds which are particularly useful are reaction products of quaternizing esters in the form of alkyl and alkenyl halides, sulfates and sulfonates containing from one to four carbon atoms, exemplified by methyl chloride, ethyl chloride, methyl chloracetate, and one and two carbon atom alkyl sulfates; or aromatic quaternizing esters in the form of halides, sulfates and sulfonates advantageously containing from seven to nine carbon atoms, exemplified by benzyl chlorides, dimethylbenzyl chloride, and phenylethyl chloride, with adducts of (0) alkyl amines having a reactive hydrogen and containing from one to four carbon atoms, such as dimethylamine and diethylamine with (b) propyleneoxide or butyleneoxides, said adducts containing 1 mol of (a) to from 6, and preferably from 8, to 30 mols of (b).
it is important to note that it is critical to the successful formulation of the compositions of the present invention that the oxyalkylene groups substituted on the quaternary ammonium type compounds be derived from an a-epoxide containing at least three carbon atoms. The most important embodiment of the a-epoxide whose use is contemplated herein in the production of the desired quaternary ammonium type compounds is propyleneoxide The a epoxides containing four, five, six or more carbon atoms can be used but, for general reasons of lack of economy or commercial availability, are not preferred. Typical of such latter a-epoxides are butyleneoxides such as l,2-butyleneoxide, pentylene epoxides, hexylene epoxides, heptylene epoxides, octylene epoxides, dodecylene epoxides, and C C, olefin oxides or epoxides, and, as well, styrene epoxide. It will be seen that most of those of the a-epoxides in which the vicinal carbons are terminal can conveniently by represented by the formula where R is an alkyl radical. In the case of propylene oxide, R is CH and in the representation of the group of propyleneoxide, butyleneoxides, pentyleneoxide and hexyleneoxide R contains from one to four carbon atoms. In the higher molecular weight alkylene oxides, R may contain as high as 16 carbon atoms.
While ethylene oxide cannot be employed as the sole alkylene oxide in preparing the quaternary ammonium cationic surfactants useful in preparing the novel anionic-cationic surfactant compositions of the present invention, minor proportions thereof, not to exceed about 20 percent by weight of the propylene oxide, or other a-epoxide employed, can be utilized as hereafter described. Mixtures of two or more of the a-epoxides containing at least three carbon atoms can, of course, be used as such, as well as in conjunction with ethylene oxide, subject to the limitation that the ethylene oxide must not exceed the aforesaid 20 percent of the weight of said a-epoxides.
The radical A can be any negative or salt-forming radical as, for instance, halogen such as chlorine, bromine and iodine; hydroxy; sulfate, alkyl-sulfuric acid such as methyl sulfuric acid or ethyl sulfuric acid (methosulfate of ethosulfate); nitrate; phosphate; acetate; formate; carbonate; lower alkyl (one to four carbon atoms) sulfonic acids; and the like. Of particular importance are those of the quaternary ammonium type compounds in which the anion is chlorine, bromine, methyl chloracetate, methosulfate, and ethosulfate. Various of said anionic radicals can be introduced directly into the molecules; and, in the case of others, they can be made, for instance, by substitution for halogen in the quaternary ammonium type compounds employed by known techniques as, for instance, by metathesis procedures.
The anionic surfactants which are compatible with the aforesaid quaternary ammonium compounds described herein, which mixtures form the novel compositions of the present invention, comprise a broad spectrum of compounds, as is well known to those skilled in the art. Members of this classification comprise the water-soluble salts such as the alkali metal and amine soaps of straight and branched chain fatty acids, said fatty acids being both naturally occurring, such as from coconut oil or from tall oil, and synthetically produced such as by paraffin oxidation; the water soluble salts of organic sulfonic acids, alkyl sulfuric acids and sulfuric acid esters of polyhydric alcohols incompletely esterified with a fatty acid of high molecular weight, sulfated and sulfonated higher fatty acid amides and alkanolamides which include the sulfated fatty oil, sulfated fatty acids, sulfated straight chain and branched chain C -C alcohols, sulfated alkylolamides and the like. The more important of this group are the alkyl sulfates prepared by reacting a fatty alcohol with sulfuric acid or chlorosulfonic acid, said fatty alcohol having from about eight to 18 carbon atoms, of particular utility in preparing the compositions of the present invention being the alkali metal, alkaline earth metal, ammonium, lower amine and a1- kanolamine alkyl sulfates wherein the alkyl group contains from eight to 18 carbon atoms.
Other compatible anionic surfactants useful in preparing the compositions of the present invention are the alkanesulfonates, esterand ether-linked sulfonates such as the di-alkyl sulfo-succinates, amide linked sulfonates and various derivatives thereof. Also suitable are the well known alkylaryl sulfonates, both straight and branched chain, sodium dodecylbenzene sulfonate being the common commercial product. These alkylaryl sulfonates usually contain from about six to 26 carbon atoms in the alkyl chain. The aforesaid alkylaryl sulfonates may also contain intermediate linkages such as amide and hydrazide linkages, as exemplified by the sulfonated a-alkylbenzimidazoles, and ester and ether linkages. Further types of suitable anionic surfactants are the esters of the oxy acids of phosphorous with aliphatic alcohols having from about six to 18 carbon atoms and alkyl phenols wherein the alkyl chain contains from eight to 18 carbon atoms.
Especially suitable and preferred are anionic detergents wherein the anionic surfactant solubilizing group is a member selected from the group consisting of SO H, SO H, COOH and the water-soluble salts thereof especially the alkali metal, alkaline earth metal, ammonium and lower amine and alkanolamine salts.
The anionic surfactants are disclosed in numerous patents among which may be mentioned, by way of illustration, U.S. Pat. Nos. 2,383,737; 2,486,921; 2,920,045; and 3,004,056.
Broadly speaking, the aforesaid quaternary ammonium surfactant may be combined with the aforesaid anionic surfactants over a wide range of proportions, since the compatibility is not limited by any critical weight proportions, and there will be no significant diminution of surface active properties, no matter what the ratio of the said surfactants may be to each other. Preferably, in order to realize the foam boosting effect of the combination of anionic surfactant and the aforesaid quaternary ammonium surfactant, there is employed from about 20 to 40 percent, better still about 25 to 30 percent, of said quaternary ammonium surfactant, based on the weight of combined cationic and anionic surfactants in the compositions.
The following examples are illustrative of the practice of the present invention but are not to be considered as limitativc of its scope.
EXAMPLE 1 The following tabulated data represent the results of the Shake Foam Test (50 mls total liquid in 250 ml cylinder, 20 inversions). The anionic surfactant employed was sodium lauryl sulfate; the cationic surfactant was a quaternary ammonium compound of the formula Cg: Cal-I /1 CH3 R Cl but a cationic surfactant similar to that in Example 1 was employed except the polyoxypropylene radical contained about 30 oxypropylene groups.
TABLE 2 Shake Foam Test Foam Height Conc. Conc. Hard Water Anionic Cationic (342 p.p.m.)
EXAMPLE 3 The shake foa'm test was repeated with the cationic surfac- 40 tant of Example 1 and the triethanolamine salt of dodecylbenzene sulfonic acid as the anionic surfactant.
TABLE 3 Shake Foam Test Foam Height Conc. Conc. Distilled Hard Water Anionic Cationic Water (342p.p.m.)
EXAMPLE 4 The Shake Foam Test was repeated utilizing coconut oil soap as the anionic surfactant and the cationic surfactant of TABLE 1 Shake Foam Test Foam Height Conc. Conc. Distilled Hard Water Anionic Cationic Water 342p.p.m.
Example 1:
TABLE 4 Shake Foam Test Foam Height Conc. Anionic Conc. Cationic Distilled Water EXAMPLE An illustrative liquid shampoo formulation utilizing an illustrative cationic quaternary ammonium compound described herein with an illustrative anionic surfactant is given below.
'l'riethanulaminc lauryl sulfate [5% Lnnolin 2% Uleyl Alcohol l% llcxachlorophene 1% Propoxylutud Quaternary 8% Water 73% Compound formed by quaternizing a condensation product of 1 mol of diethyl ethanolamine and 25 moles of propyleneoxide with methyl chloride. Here the quaternary acts simultaneously as a surfactant, foam boosting agent and solubilizer for hexachlorophene.
Additional illustrative examples of compositions made in accordance with the present invention are as follows, the pro portions stated being in weight percent.
EXAMPLE 6 Phosphate ester of [0 mol ethylene oxide adduct of nonyl phenol (sodium salt) 25 mol propylene oxide adduct of dimethylamine quaternized with ethyl chloride EXAMPLE 7 Phosphate ester of 12 mol ethylene oxide adduct of dodecyl alcohol (triethanolamine salt) 16 mol propylene oxide adduct of methylethylamine quaternized with benzyl chloride EXAMPLE 8 Laurie acid monoester of sulfuric acid monoester of glycerol (triethanolamine salt) 18 mol propylene oxide adduct of dimethylethanolamine quatemized with methyl chloracetate EXAMPLE 9 Sodium lauryl sulfate 70% 12 mol butylene oxide adduct of dimethylamine quaternized with dimethyl sulfate wherein R is alkyl containing from one to three carbon atoms, R, is a member selected from the group consisting of alkyl containing from one to three carbon atoms and and compounds wherein R and R are joined together to form with the N atom a member of the group consisting of piperidine, methyl piperidine and pyrrolidiene; R is where R, is alkyl containing from one to four carbon atoms, n and n are numbers the sum of which does not exceed 60, the total number of carbon atoms in R, being at least 18; R is a member selected from the group consisting of alkyl and alkenyl containing from one to four carbon atoms; benzene; methyl benzenes; ethyl benzenes;
and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo mono-nitro nuclearly substituted derivatives of the foregoing; and A is an anion.
2. A composition according to claim 1 wherein the anionic surfactant is selected from the group consisting of alkyl sulfates, alkylaryl sulfonates and fatty carboxylic acid soaps 3. A composition according to claim 2 wherein the anionic surfactant is an alkali metal alkyl sulfate wherein the alkyl group contains from eight to 18 carbon atoms.
4. A composition according to claim 2 wherein the anionic surfactant is an alkali metal alkyl benzene sulfonate wherein the alkyl group contains from eight to 18 carbon atoms.
5. A composition according to claim 1 in which the R radical of said cationic surfactant compound contains a polyoxyethylene radical in which the ethylene oxide constitutes not more than 20 percent by weight of said R radical.
6. A composition according to claim 1 in which the R and R radicals of said quaternary ammonium compound are joined together to form with the N atom a cyclic amine containing not more than six carbon atoms, with the proviso that the total number of carbon atoms in R and R does not exceed 6; and R is polyoxyalkylene containing at least 18 carbon atoms and derived from an a-epoxide containing from three to six carbon atoms.
7. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, etherand amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is alkyl containing from one to three carbon atoms, R, is
CH CH-O- 2' I 1&4 n
and R is where R is alkyl containing from one to four carbon atoms, n and n are numbers the sum of which does not exceed 60, the total number of carbon atoms in R, and R being at least 18; R is a member selected from the group consisting of l alkyl and alkenyl containing not more than four carbon atoms, and (2)benzene; methyl benzenes', ethyl benzenes;
alkylaryl sulfonates and phosphates of aliphatic alcohols and 10 alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is alkyl containing from one to three carbon atoms, R is alkyl containing from one to three carbon atoms, alkylenc contains not more than three carbon atoms, R is where R, is alkyl containing from one to four carbon atoms, n is a number up to and including 60, the total number of carbon atoms in R being at least 18; R-; is a member selected from the group consisting of (1) alkyl and alkenyl containing not more than four carbon atoms, and (2) benzene; methyl benzenes; ethyl benzenes:
and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo and mono-nitro nuclearly substituted derivatives of the foregoing; and A is an innocuous anion.
9. A composition consisting essentially of a water-soluble I anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, etherand amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is alkyl containing from one to three carbon atoms, alkylene contains not more than three carbon atoms, R,-0 is and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo and mono-nitro nuclearly substituted derivatives of the foregoing; and A is an innocuous anion.
10. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, etherand amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on theweight of combined cationic and anionic surfactants, corresponding to the formula where alkylene contains not more than three carbon atoms,
in which R is alkyl containing from one to four carbon atoms, n, n and n are numbers the sum of which does not exceed 60, the total number of carbon atoms in R, R and R being at least 18; R is a member selected from the group consisting of 1) alkyl and alkenyl containing not more than four carbon atoms, and (2)benzene; methyl benzenes; ethyl benzenes;
and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo and mono-nitro nuclearly substituted derivatives of the foregoing; and A is an innocuous anion.
11. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, etherand amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is alkyl containing from one to three carbon atoms, R is selected from the group consisting of alkyl containing from one to three carbon atoms and hydroxyalkyl containing from two to four carbon atoms, R, is a polyoxyalkylene substituent containing at least 18 carbon atoms and derived from an a-epoxide containing from three to eight carbon atoms, R is a member selected from the group consisting of 1 a hydroxyalkyl containing from two to four carbon atoms, and (2) benzene; methyl benzenes; ethyl benzenes;
polyhydric alcohols partially esterified with a fatty acid,
sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, etherand amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where alkylene contains not more than three carbon atoms, R-O- R1 is and R is and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo and mono-nitro nuclearly substituted derivatives of the foregoing; and A is an innocuous anion.
13. A composition consisting essentially of a water insoluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, ether and amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula one to four carbon atoms, n total number of carbon where R, is alkyl containing from is a number up to and including 60, the
atoms is R; being at least 18, v is a number at least 1 with the proviso that the weight ratio of (C Ht0-), to R is not greater than one to four, X is a member selected from the group consisting of (l alkyl and alkenyl containing from one to four carbon atoms, and (2) benzene; lower alkyl benzenes in which the lower alkyl contain from one to four carbon and their methyl and ethyl nuclearly substituted derivatives;
and the mono-halo, mono-nitro and mono-sulfonic nuclearly substituted derivatives of the foregoing; and A is an anion.
14. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane' sulfonates, ester-, etherand amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and lakyl phenols and from about 20 to alkyl percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula A C2H4 0' )v 2 where R is alkyl containing from one to three carbon atoms, R, is
where R is alkyl containing from one to four carbon atoms, n is a number up to and including 60, the total number of carbon atoms in R being at least 18, v is a number at least 1 with the proviso that the weight ratio of (C H -O-),. to R is not greater than one to four, X is a member selected from the group consisting of l alkyl and alkenyl containing from one to four carbon atoms, and benzene; lower alkyl benzenes in which the lower alkyls contain from one to four carbon atoms,
and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo, mono-nitro and mono-sulfonic nuclearly substituted derivatives of the foregoing; and A is an anion.
15 A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, etherand amide linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R and R are the same or dissimilar alkyls each containing from 1 to 3 carbon atoms, R,-O-R is polyoxyethylenepolyoxypropylene containing at least 6 oxypropylene groups and where the weight ratio of the polyoxyethylene to the polyoxypropylene is not greater than one to four, the total number of oxypropylene groups not exceeding 60, X is a member selected from the group consisting of l alkyl and al- IOIO39 0178 kenyl containing from one four carbon atoms, and (2) benzene; lower alkyl benzenes in which the lower alkyls contain from one to four carbon atoms,
alkyl phenols and from about to 40 percent bysweight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is alkyl containing from one to three carbon atoms, R,OR is polyoxyethylene-polyoxypropylene containing at least 6 oxypropylene groups and where the weight ratio of the polyoxyethylene to the polyoxypropylene is not greater than one to four, the total number of oxypropylene groups not exceeding 60, X is a member selected from the group consisting of 1) alkyl and alkenyl containing from one to four carbon atoms, and benzene; lower alkyl benzenes in which the lower alkyls contain from one to four carbon atoms,
and their methyl and ethyl nuclearly substituted derivatives; and the monohalo, mono-nitro and mono-sulfonic nuclearly substituted derivatives of the foregoing; and A is an anion.
17. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, etherand amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is an alkyl containing from one to three carbon atoms R is greater than one to four, X is a member selected from the group consisting of 1) alkyl and alkenyl containing from one to four carbon atoms, and (2) benzene; lower alkyl benzenes in which the lower alkyls contain from one to four carbon atoms,
and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo, mono-nitro and mono-sulfonic nuclearly substituted derivatives of the foregoing; and A is an anion.
18. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, etherand amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is alkyl containing from one to three carbon atoms,
R is
and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo, mono-nitro and mono-sulfonic nuclearly substituted derivatives of the foregoing; and A is an anion.
19. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, etherand amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is alkyl containing from one to three carbon atoms, R alkyl containing from one to three carbon atoms, R is and n totals a number from 8 to 30, X is a member selected from the group consisting of 1) alkyl and alkenyl containing from one to four carbon atoms, and (2) benzene; lower alkyl benzenes in which the lower alkyls contain from one to four carbon atoms,
and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo, mono-nitro and mono-sulfonic nuclearly substituted derivatives of the foregoing; and A is an anion.
20. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, etherand amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent, by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula and R is alkyl containing from one to four carbon atoms, and n totals a number not exceeding 60 with the proviso that the number of carbon atoms in the total of the R, radicals is at least 18, v is a number at leat l with the proviso that the weight ratio of (C,l-l,--O) to R, is not greater than one to four, X is a member selected from the group consisting of l alkyl and alkenyl containing from one to four carbon atoms, and (2) benzene; lower alkyl benzenes in which the lower alkyls contain from one to four carbon atoms,
and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo, mono-nitro and mono-sulfonic nuclearly substituted derivatives of the foregoing; and A is an anion.
Claims (19)
- 2. A composition according to claim 1 wherein the anionic surfactant is selected from the group consisting of alkyl sulfates, alkylaryl sulfonates and fatty carboxylic acid soaps.
- 3. A composition according to claim 2 wherein the anionic surfactant is an alkali metal alkyl sulfate wherein the alkyl group contains from eight to 18 carbon atoms.
- 4. A composition according to claim 2 wherein the anionic surfactant is an alkali metal alkyl benzene sulfonate wherein the alkyl group contains from eight to 18 carbon atoms.
- 5. A composition according to claim 1 in which the R2 radical of said cationic surfactant compound contains a polyoxyethylene radical in which the ethylene oxide constitutes not more than 20 percent by weight of said R2 radical.
- 6. A composition according to claim 1 in which the R and R1 radicals of said quaternary ammonium compound are joined togeTher to form with the N atom a cyclic amine containing not more than six carbon atoms, with the proviso that the total number of carbon atoms in R and R1 does not exceed 6; and R2 is polyoxyalkylene containing at least 18 carbon atoms and derived from an Alpha -epoxide containing from three to six carbon atoms.
- 7. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, ether- and amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula
- 8. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, ether- and amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula
- 9. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, ether- and amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula
- 10. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, ether- and amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula
- 11. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, ether- and amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula
- 12. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, ether- and amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula
- 13. A composition consisting essentially of a water insoluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, ether- and amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R and R1 are the same or dissimilar alkyls each containing from one to three carbon atoms, R2 is where R3 is alkyl containing from one to four carbon atoms, n is a number up to and including 60, the total number of carbon atoms is R2 being at least 18, v is a number at least 1 with the proviso that the weight ratio of (C2H4-0-)v to R2 is not greater than one to four, X is a member selected from the group consisting of (1) alkyl and alkenyl containing from one to four carbon atoms, and (2) benzene; lower alkyl benzenes in which the lower alkyl contain from one to four carbon atoms, and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo, mono-nitro and mono-sulfonic nuclearly substituted derivatives of the foregoing; and A is an anion.
- 14. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, ether- and amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and lakyl phenols and from about 20 to alkyl percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is alkyl containing from one to three carbon atoms, R2 is where R3 is alkyl containing from one to four carbon atoms, n is a number up to and including 60, the total number of carbon atoms in R2 being at least 18, v is a number at least 1 with the proviso that the weight ratio of (C2H4-O-)v to R2 is not greater than one to four, X is a member selected from the group consisting of (1) alkyl and alkenyl containing from one to four carbon atoms, and benzene; lower alkyl benzenes in which the lower alkyls contain from one to four carbon atoms, and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo, mono-nitro and mono-sulfonic nuclearly substituted derivatives of the foregoing; and A is an anion.
- 15. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, ether- and amide-linked sulfonates, alkYlaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R and R1 are the same or dissimilar alkyls each containing from 1 to 3 carbon atoms, R4-O-R5 is polyoxyethylene-polyoxypropylene containing at least 6 oxypropylene groups and where the weight ratio of the polyoxyethylene to the polyoxypropylene is not greater than one to four, the total number of oxypropylene groups not exceeding 60, X is a member selected from the group consisting of (1) alkyl and alkenyl containing from one four carbon atoms, and (2) benzene; lower alkyl benzenes in which the lower alkyls contain from one to four carbon atoms, and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo, mono-nitro and mono-sulfonic nuclearly substituted derivatives of the foregoing; and A is an anion.
- 16. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides. alkane-sulfonates, ester-, ether- and amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is alkyl containing from one to three carbon atoms, R4-O-R5 is polyoxyethylene-polyoxypropylene containing at least 6 oxypropylene groups and where the weight ratio of the polyoxyethylene to the polyoxypropylene is not greater than one to four, the total number of oxypropylene groups not exceeding 60, X is a member selected from the group consisting of (1) alkyl and alkenyl containing from one to four carbon atoms, and benzene; lower alkyl benzenes in which the lower alkyls contain from one to four carbon atoms, and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo, mono-nitro and mono-sulfonic nuclearly substituted derivatives of the foregoing; and A is an anion.
- 17. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, ether- and amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is an alkyl containing from one to three carbon atoms R2 is
- 18. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, ether- and amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is alkyl containing from one to three carbon atoms, R2 is and n totals a number from 8 to 30, X is a member selected from the group consisting of (1) alkyl and alkenyl containing from one to four carbon atoms, and (2) benzene; lower alkyl benzenes in which the lower alkyls contain from one to four carbon atoms, and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo, mono-nitro and mono-sulfonic nuclearly substituted derivatives of the foregoing; and A is an anion.
- 19. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, ether- and amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula where R is alkyl containing from one to three carbon atoms, R2 alkyl containing from one to three carbon atoms, R2 is and n totals a number from 8 to 30, X is a member selected from the group consisting of (1) alkyl and alkenyl containing from one to four carbon atoms, and (2) benzene; lower alkyl benzenes in which the lower alkyls contain from one to four carbon atoms, and their methyl and ethyl nuclearly substituted derivatives; and the mono-halo, mono-nitro and mono-sulfonic nuclearly substituted derivatives of the foregoing; and A is an anion.
- 20. A composition consisting essentially of a water-soluble anionic surfactant being a member selected from the group consisting of fatty acid soaps, alkyl sulfates, sulfates of polyhydric alcohols partially esterified with a fatty acid, sulfated and sulfonated fatty acid amides and alkanolamides, alkane-sulfonates, ester-, ether- and amide-linked sulfonates, alkylaryl sulfonates and phosphates of aliphatic alcohols and alkyl phenols and from about 20 to 40 percent, by weight of a cationic surfactant, based on the weight of combined cationic and anionic surfactants, corresponding to the formula
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US83969869A | 1969-07-07 | 1969-07-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3668136A true US3668136A (en) | 1972-06-06 |
Family
ID=25280425
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US839698A Expired - Lifetime US3668136A (en) | 1969-07-07 | 1969-07-07 | Compatible anionic-catonic surfactant compositions |
Country Status (4)
Country | Link |
---|---|
US (1) | US3668136A (en) |
DE (1) | DE2025481A1 (en) |
FR (1) | FR2054161A5 (en) |
GB (1) | GB1320566A (en) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2397476A1 (en) * | 1977-07-11 | 1979-02-09 | Richardson Co | ACID BATH INTENDED FOR THE PRODUCTION OF A BRILLIANT ELECTROLYTIC DEPOSIT OF ZINC AND ITS APPLICATIONS |
US4247538A (en) * | 1978-09-05 | 1981-01-27 | Witco Chemical Corporation | Conditioning shampoo |
US4303543A (en) * | 1979-02-27 | 1981-12-01 | The Procter & Gamble Company | Method for cleansing and conditioning the skin |
US4664848A (en) * | 1982-12-23 | 1987-05-12 | The Procter & Gamble Company | Detergent compositions containing cationic compounds having clay soil removal/anti-redeposition properties |
JPH05194152A (en) * | 1991-09-12 | 1993-08-03 | Unilever Nv | Hair conditioning composition |
US5298193A (en) * | 1989-04-06 | 1994-03-29 | Hoechst Aktiengesellschaft | Low-foaming and low-temperature-stable liquid surfactant compositions composed of water and nonionic, anionic and cationic surfactants and the use thereof |
WO1997043371A2 (en) * | 1996-05-17 | 1997-11-20 | The Procter & Gamble Company | Detergent composition |
WO1997044420A2 (en) * | 1996-05-17 | 1997-11-27 | The Procter & Gamble Company | Detergent composition |
WO1997044425A2 (en) * | 1996-05-17 | 1997-11-27 | The Procter & Gamble Company | Detergent composition |
WO2000063331A1 (en) * | 1999-04-20 | 2000-10-26 | Ecolab Inc. | Composition and method for road-film removal |
US6339054B1 (en) | 1999-04-20 | 2002-01-15 | Ecolab, Inc. | Composition and method for road-film removal |
US6551974B1 (en) | 1999-04-20 | 2003-04-22 | Ecolab Inc. | Polish compositions for gloss enhancement, and method |
US8557756B2 (en) | 2010-06-29 | 2013-10-15 | Dow Global Technologies Llc | Compatible mixtures of anionic and cationic surfactants |
CN116023308A (en) * | 2021-10-26 | 2023-04-28 | 中国石油化工股份有限公司 | Thickened oil viscosity reducer and preparation method and application thereof |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5352799A (en) * | 1976-10-19 | 1978-05-13 | Kao Corp | Fabric softening agent composition |
JPS5527134A (en) * | 1978-08-15 | 1980-02-27 | Kao Corp | Hair rinse composition |
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GB873214A (en) * | 1958-08-20 | 1961-07-19 | British Nylon Spinners Ltd | Non-ionic detergent compositions |
US3123641A (en) * | 1964-03-03 | Cation-active surface active trilower- | ||
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US3141905A (en) * | 1963-04-29 | 1964-07-21 | Witco Chemical Corp | Cation-active surface active quaternary ammonium compounds |
US3155591A (en) * | 1961-12-06 | 1964-11-03 | Witco Chemical Corp | Hair rinse compostions of polyoxypropylene quaternary ammonium compounds |
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-
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- 1969-07-07 US US839698A patent/US3668136A/en not_active Expired - Lifetime
-
1970
- 1970-05-25 DE DE19702025481 patent/DE2025481A1/en active Pending
- 1970-06-15 GB GB2367570A patent/GB1320566A/en not_active Expired
- 1970-07-03 FR FR7024856A patent/FR2054161A5/fr not_active Expired
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US3123641A (en) * | 1964-03-03 | Cation-active surface active trilower- | ||
US3123640A (en) * | 1964-03-03 | Cation-active surface active aryldi- | ||
US3345300A (en) * | 1967-10-03 | Ohj-ohi | ||
US2734830A (en) * | 1950-01-13 | 1956-02-14 | ||
GB873214A (en) * | 1958-08-20 | 1961-07-19 | British Nylon Spinners Ltd | Non-ionic detergent compositions |
US3155591A (en) * | 1961-12-06 | 1964-11-03 | Witco Chemical Corp | Hair rinse compostions of polyoxypropylene quaternary ammonium compounds |
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Cited By (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2397476A1 (en) * | 1977-07-11 | 1979-02-09 | Richardson Co | ACID BATH INTENDED FOR THE PRODUCTION OF A BRILLIANT ELECTROLYTIC DEPOSIT OF ZINC AND ITS APPLICATIONS |
US4247538A (en) * | 1978-09-05 | 1981-01-27 | Witco Chemical Corporation | Conditioning shampoo |
US4303543A (en) * | 1979-02-27 | 1981-12-01 | The Procter & Gamble Company | Method for cleansing and conditioning the skin |
US4664848A (en) * | 1982-12-23 | 1987-05-12 | The Procter & Gamble Company | Detergent compositions containing cationic compounds having clay soil removal/anti-redeposition properties |
US5298193A (en) * | 1989-04-06 | 1994-03-29 | Hoechst Aktiengesellschaft | Low-foaming and low-temperature-stable liquid surfactant compositions composed of water and nonionic, anionic and cationic surfactants and the use thereof |
JPH05194152A (en) * | 1991-09-12 | 1993-08-03 | Unilever Nv | Hair conditioning composition |
US6136769A (en) * | 1996-05-17 | 2000-10-24 | The Procter & Gamble Company | Alkoxylated cationic detergency ingredients |
WO1997044420A2 (en) * | 1996-05-17 | 1997-11-27 | The Procter & Gamble Company | Detergent composition |
WO1997044425A2 (en) * | 1996-05-17 | 1997-11-27 | The Procter & Gamble Company | Detergent composition |
WO1997044425A3 (en) * | 1996-05-17 | 1997-12-24 | Procter & Gamble | Detergent composition |
WO1997044420A3 (en) * | 1996-05-17 | 1997-12-24 | Procter & Gamble | Detergent composition |
WO1997043371A3 (en) * | 1996-05-17 | 1997-12-24 | Procter & Gamble | Detergent composition |
WO1997043371A2 (en) * | 1996-05-17 | 1997-11-20 | The Procter & Gamble Company | Detergent composition |
US6602350B2 (en) | 1999-04-20 | 2003-08-05 | Ecolab Inc. | Composition and method for road-film removal |
US7223722B2 (en) | 1999-04-20 | 2007-05-29 | Ecolab Inc. | Polish compositions for gloss enhancement, and method |
US6350725B1 (en) | 1999-04-20 | 2002-02-26 | Ecolab, Inc. | Composition and method for road-film removal |
US6551974B1 (en) | 1999-04-20 | 2003-04-22 | Ecolab Inc. | Polish compositions for gloss enhancement, and method |
WO2000063331A1 (en) * | 1999-04-20 | 2000-10-26 | Ecolab Inc. | Composition and method for road-film removal |
US6864220B2 (en) | 1999-04-20 | 2005-03-08 | Ecolab Inc. | Composition and method for road-film removal |
US20050199272A1 (en) * | 1999-04-20 | 2005-09-15 | Ecolab Inc. | Composition and method for road-film removal |
US6339054B1 (en) | 1999-04-20 | 2002-01-15 | Ecolab, Inc. | Composition and method for road-film removal |
US7482315B2 (en) | 1999-04-20 | 2009-01-27 | Ecolab Inc. | Composition and method for road-film removal |
US20090188533A1 (en) * | 1999-04-20 | 2009-07-30 | Ecolab Inc. | Composition and method for road-film removal |
US7951245B2 (en) | 1999-04-20 | 2011-05-31 | Ecolab Usa Inc. | Composition and method for road-film removal |
US8557756B2 (en) | 2010-06-29 | 2013-10-15 | Dow Global Technologies Llc | Compatible mixtures of anionic and cationic surfactants |
CN116023308A (en) * | 2021-10-26 | 2023-04-28 | 中国石油化工股份有限公司 | Thickened oil viscosity reducer and preparation method and application thereof |
CN116023308B (en) * | 2021-10-26 | 2024-05-03 | 中国石油化工股份有限公司 | Thickened oil viscosity reducer and preparation method and application thereof |
Also Published As
Publication number | Publication date |
---|---|
GB1320566A (en) | 1973-06-13 |
DE2025481A1 (en) | 1971-01-14 |
FR2054161A5 (en) | 1971-04-16 |
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