EP0018039B1 - Fabric softening composition - Google Patents
Fabric softening composition Download PDFInfo
- Publication number
- EP0018039B1 EP0018039B1 EP80200320A EP80200320A EP0018039B1 EP 0018039 B1 EP0018039 B1 EP 0018039B1 EP 80200320 A EP80200320 A EP 80200320A EP 80200320 A EP80200320 A EP 80200320A EP 0018039 B1 EP0018039 B1 EP 0018039B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- alkyl
- water
- mono
- alkenyl
- mixture
- 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
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 107
- 239000004744 fabric Substances 0.000 title claims abstract description 14
- -1 fatty acid ester Chemical class 0.000 claims abstract description 36
- 239000003093 cationic surfactant Substances 0.000 claims abstract description 23
- 125000002091 cationic group Chemical group 0.000 claims abstract description 20
- 239000004094 surface-active agent Substances 0.000 claims abstract description 18
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 17
- 239000000194 fatty acid Substances 0.000 claims abstract description 17
- 229930195729 fatty acid Natural products 0.000 claims abstract description 17
- 239000004665 cationic fabric softener Substances 0.000 claims abstract description 15
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 11
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 8
- 125000003342 alkenyl group Chemical group 0.000 claims description 24
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 17
- 150000003839 salts Chemical class 0.000 claims description 16
- 239000012188 paraffin wax Substances 0.000 claims description 15
- 150000002148 esters Chemical class 0.000 claims description 9
- 150000003863 ammonium salts Chemical class 0.000 claims description 4
- 125000005466 alkylenyl group Chemical group 0.000 claims description 2
- 230000002209 hydrophobic effect Effects 0.000 abstract description 17
- 239000006185 dispersion Substances 0.000 abstract description 7
- 239000000463 material Substances 0.000 description 32
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical group C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 12
- 239000002752 cationic softener Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000001257 hydrogen Substances 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000003760 tallow Substances 0.000 description 4
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 4
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 3
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000007983 Tris buffer Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000013459 approach Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 150000004820 halides Chemical class 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 239000004753 textile Substances 0.000 description 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- IZHVBANLECCAGF-UHFFFAOYSA-N 2-hydroxy-3-(octadecanoyloxy)propyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)COC(=O)CCCCCCCCCCCCCCCCC IZHVBANLECCAGF-UHFFFAOYSA-N 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Chemical group 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical class C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 239000004902 Softening Agent Substances 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- PGZPBNJYTNQMAX-UHFFFAOYSA-N dimethylazanium;methyl sulfate Chemical compound C[NH2+]C.COS([O-])(=O)=O PGZPBNJYTNQMAX-UHFFFAOYSA-N 0.000 description 2
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical group [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 230000002708 enhancing effect Effects 0.000 description 2
- MVLVMROFTAUDAG-UHFFFAOYSA-N ethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC MVLVMROFTAUDAG-UHFFFAOYSA-N 0.000 description 2
- 239000002979 fabric softener Substances 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- 150000002431 hydrogen Chemical group 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 229940037626 isobutyl stearate Drugs 0.000 description 2
- 229960004592 isopropanol Drugs 0.000 description 2
- CPXCDEMFNPKOEF-UHFFFAOYSA-N methyl 3-methylbenzoate Chemical compound COC(=O)C1=CC=CC(C)=C1 CPXCDEMFNPKOEF-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 description 2
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 2
- RZJRJXONCZWCBN-UHFFFAOYSA-N octadecane Chemical compound CCCCCCCCCCCCCCCCCC RZJRJXONCZWCBN-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229940100515 sorbitan Drugs 0.000 description 2
- 241000894007 species Species 0.000 description 2
- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical class CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 description 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- ZPFAVCIQZKRBGF-UHFFFAOYSA-N 1,3,2-dioxathiolane 2,2-dioxide Chemical compound O=S1(=O)OCCO1 ZPFAVCIQZKRBGF-UHFFFAOYSA-N 0.000 description 1
- WSULSMOGMLRGKU-UHFFFAOYSA-N 1-bromooctadecane Chemical compound CCCCCCCCCCCCCCCCCCBr WSULSMOGMLRGKU-UHFFFAOYSA-N 0.000 description 1
- RNHWYOLIEJIAMV-UHFFFAOYSA-N 1-chlorotetradecane Chemical compound CCCCCCCCCCCCCCCl RNHWYOLIEJIAMV-UHFFFAOYSA-N 0.000 description 1
- FKOKUHFZNIUSLW-UHFFFAOYSA-N 2-Hydroxypropyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(C)O FKOKUHFZNIUSLW-UHFFFAOYSA-N 0.000 description 1
- WOUANPHGFPAJCA-UHFFFAOYSA-N 2-[benzyl(methyl)amino]ethanol Chemical class OCCN(C)CC1=CC=CC=C1 WOUANPHGFPAJCA-UHFFFAOYSA-N 0.000 description 1
- FAEIVMXWKPDFTP-UHFFFAOYSA-N 2-[dodecyl(methyl)amino]ethane-1,1-diol Chemical class CCCCCCCCCCCCN(C)CC(O)O FAEIVMXWKPDFTP-UHFFFAOYSA-N 0.000 description 1
- YINFMGHGSSYIBL-UHFFFAOYSA-N 2-[hexadecyl(methyl)amino]ethane-1,1-diol Chemical class CCCCCCCCCCCCCCCCN(C)CC(O)O YINFMGHGSSYIBL-UHFFFAOYSA-N 0.000 description 1
- SBAOEHHCKZJQAY-UHFFFAOYSA-N 2-[methyl(octadecyl)amino]ethane-1,1-diol Chemical class CCCCCCCCCCCCCCCCCCN(C)CC(O)O SBAOEHHCKZJQAY-UHFFFAOYSA-N 0.000 description 1
- LWLRMRFJCCMNML-UHFFFAOYSA-N 2-ethylhexyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(CC)CCCC LWLRMRFJCCMNML-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- WYWPHTQMLPHMKP-UHFFFAOYSA-N 2-hydroxyethyl-dimethyl-tetradecylazanium Chemical class CCCCCCCCCCCCCC[N+](C)(C)CCO WYWPHTQMLPHMKP-UHFFFAOYSA-N 0.000 description 1
- OFAOJFWUXOUJSL-XXAVUKJNSA-N 3-[3-[bis(3-hydroxypropyl)amino]propyl-[(z)-octadec-9-enyl]amino]propan-1-ol;dihydrofluoride Chemical compound F.F.CCCCCCCC\C=C/CCCCCCCCN(CCCO)CCCN(CCCO)CCCO OFAOJFWUXOUJSL-XXAVUKJNSA-N 0.000 description 1
- YLWLITGYHXXWHR-UHFFFAOYSA-N 3-[3-[bis(3-hydroxypropyl)amino]propyl-hexadecylamino]propan-1-ol;dihydrobromide Chemical compound Br.Br.CCCCCCCCCCCCCCCCN(CCCO)CCCN(CCCO)CCCO YLWLITGYHXXWHR-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 1
- HMRWHRBSEMHEFA-UHFFFAOYSA-N 6-methylheptyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCCCCCC(C)C HMRWHRBSEMHEFA-UHFFFAOYSA-N 0.000 description 1
- 244000291564 Allium cepa Species 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 239000004386 Erythritol Substances 0.000 description 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001345 alkine derivatives Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- FLNKWZNWHZDGRT-UHFFFAOYSA-N azane;dihydrochloride Chemical compound [NH4+].[NH4+].[Cl-].[Cl-] FLNKWZNWHZDGRT-UHFFFAOYSA-N 0.000 description 1
- BXJTWXJUYOEABN-UHFFFAOYSA-N benzyl-(2-hydroxyethyl)-methyl-tetradecylazanium Chemical class CCCCCCCCCCCCCC[N+](C)(CCO)CC1=CC=CC=C1 BXJTWXJUYOEABN-UHFFFAOYSA-N 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- RLGQACBPNDBWTB-UHFFFAOYSA-N cetyltrimethylammonium ion Chemical class CCCCCCCCCCCCCCCC[N+](C)(C)C RLGQACBPNDBWTB-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- VKKVMDHHSINGTJ-UHFFFAOYSA-M di(docosyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCCCCCC VKKVMDHHSINGTJ-UHFFFAOYSA-M 0.000 description 1
- OCTAKUVKMMLTHX-UHFFFAOYSA-M di(icosyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCCCC OCTAKUVKMMLTHX-UHFFFAOYSA-M 0.000 description 1
- HPDYVEVTJANPRA-UHFFFAOYSA-M diethyl(dihexadecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](CC)(CC)CCCCCCCCCCCCCCCC HPDYVEVTJANPRA-UHFFFAOYSA-M 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- ZCPCLAPUXMZUCD-UHFFFAOYSA-M dihexadecyl(dimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCC ZCPCLAPUXMZUCD-UHFFFAOYSA-M 0.000 description 1
- NAPSCFZYZVSQHF-UHFFFAOYSA-N dimantine Chemical class CCCCCCCCCCCCCCCCCCN(C)C NAPSCFZYZVSQHF-UHFFFAOYSA-N 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- IDROXUWVODOXTL-UHFFFAOYSA-N dodecyl-(2-hydroxyethyl)-dimethylazanium Chemical class CCCCCCCCCCCC[N+](C)(C)CCO IDROXUWVODOXTL-UHFFFAOYSA-N 0.000 description 1
- OQKFOMLUQPERBK-UHFFFAOYSA-N dodecyl-(3-hydroxypropyl)-dimethylazanium Chemical class CCCCCCCCCCCC[N+](C)(C)CCCO OQKFOMLUQPERBK-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- 229940093476 ethylene glycol Drugs 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 229960005150 glycerol Drugs 0.000 description 1
- 229940074045 glyceryl distearate Drugs 0.000 description 1
- 229940075507 glyceryl monostearate Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- QYRFJLLXPINATB-UHFFFAOYSA-N hydron;2,4,5,6-tetrafluorobenzene-1,3-diamine;dichloride Chemical compound Cl.Cl.NC1=C(F)C(N)=C(F)C(F)=C1F QYRFJLLXPINATB-UHFFFAOYSA-N 0.000 description 1
- 229940074928 isopropyl myristate Drugs 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 229940075495 isopropyl palmitate Drugs 0.000 description 1
- 229940089456 isopropyl stearate Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- RDIVLNOKDXZMJS-UHFFFAOYSA-N n'-(2-aminoethyl)ethane-1,2-diamine;trihydrochloride Chemical compound Cl.Cl.Cl.NCCNCCN RDIVLNOKDXZMJS-UHFFFAOYSA-N 0.000 description 1
- HRKICRHARITSQS-UHFFFAOYSA-N n'-(3-aminopropyl)propane-1,3-diamine;trihydrochloride Chemical compound Cl.Cl.Cl.NCCCNCCCN HRKICRHARITSQS-UHFFFAOYSA-N 0.000 description 1
- NHLUVTZJQOJKCC-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine Chemical class CCCCCCCCCCCCCCCCN(C)C NHLUVTZJQOJKCC-UHFFFAOYSA-N 0.000 description 1
- SFBHPFQSSDCYSL-UHFFFAOYSA-N n,n-dimethyltetradecan-1-amine Chemical class CCCCCCCCCCCCCCN(C)C SFBHPFQSSDCYSL-UHFFFAOYSA-N 0.000 description 1
- OMEMQVZNTDHENJ-UHFFFAOYSA-N n-methyldodecan-1-amine Chemical class CCCCCCCCCCCCNC OMEMQVZNTDHENJ-UHFFFAOYSA-N 0.000 description 1
- IHFXMTOFDQKABX-UHFFFAOYSA-N n-methylhexadecan-1-amine Chemical class CCCCCCCCCCCCCCCCNC IHFXMTOFDQKABX-UHFFFAOYSA-N 0.000 description 1
- QWERMLCFPMTLTG-UHFFFAOYSA-N n-methyltetradecan-1-amine Chemical class CCCCCCCCCCCCCCNC QWERMLCFPMTLTG-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 229940038384 octadecane Drugs 0.000 description 1
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadecene Natural products CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 125000001312 palmitoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940059574 pentaerithrityl Drugs 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- ZPWFUIUNWDIYCJ-UHFFFAOYSA-N propan-2-yl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(C)C ZPWFUIUNWDIYCJ-UHFFFAOYSA-N 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 229940093625 propylene glycol monostearate Drugs 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 229960002920 sorbitol Drugs 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 229960004793 sucrose Drugs 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- GLFDLEXFOHUASB-UHFFFAOYSA-N trimethyl(tetradecyl)azanium Chemical class CCCCCCCCCCCCCC[N+](C)(C)C GLFDLEXFOHUASB-UHFFFAOYSA-N 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/001—Softening compositions
- C11D3/0015—Softening compositions liquid
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/18—Hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2093—Esters; Carbonates
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/02—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with hydrocarbons
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/46—Compounds containing quaternary nitrogen atoms
Definitions
- This invention relates to fabric softening compositions and, in particular, to compositions in aqueous medium having improved softening effectiveness combined with excellent physical characteristics, especially formulation stability.
- Conventional rinse-added fabric softening compositions contain fabric softening agents which are substantially water-insoluble cationic materials usually having two long alkyl chains. Typical of such materials are distearyl di-methyl ammonium chloride and imidazolinium compounds substituted with two stearyl groups. These materials are normally prepared in the form of an aqueous dispersion or emulsion, and it is generally not possible to prepare such aqueous dispersions with more than about 6% of cationic material without taking special precautions to ensure acceptable viscosity and stability characteristics. Indeed, with cationic levels in excess of about 8% the problems of physical instability and high viscosity become, in the case of conventional fabric softening products, almost intractable. This, of course, limits the level of softening performance achievable with conventional compositions without using excessive amounts of product, and also adds substantially to distribution and packaging costs, because of the need to market such dilute solutions of the active ingredient.
- Formulations prepared in this manner are still not entirely satisfactory.
- the level of softness benefit delivered by such compositions on a unit active weight basis is still much lower than for conventional dilute products and problems of physical formulation characteristics, especially phase stability and also viscosity, still remain.
- an important limitation of the prior art compositions is the difficulty in meeting simultaneous product stability and viscosity characteristics. Indeed, phase stability remains a problem even in the case of dilute softener compositions formulated in the manner of the above prior art references.
- 25 03 026 discloses a complex softener/disinfec- tant composition in which a long chain fatty alcohol is suggested as a solubilization aid.
- U.S. Patent No. 3,793,196 describes an improved viscosity softening agent in the form of an oil-in- water emulsion comprising a cationic surface-active agent, a higher fatty alcohol, a sorbitan fatty acid ester and a polyethoxylated nonionic surfactant.
- the present invention accordingly provides a fabric softening composition having improved softening characteristics and cost-effectiveness combined with excellent physical characteristics, especially phase stability, freeze-thaw behaviour and low viscosity; and it further provides a concentrated fabric softening composition having satisfactory characteristics for consumer use, based on cationic fabric softener as the major active component.
- an aqueous fabric softening composition characterized by:-
- the physical form of the composition is that of a dispersion of an anisotropic softener phase in an aqueous isotropic surfactant solution phase.
- the physical form is simply determined under a polarizing microscope.
- the anisotropic/isotropic phase system is highly important for achieving optimum viscosity, stability, softening and other textile benefits.
- the water insoluble cationic fabric softener is preferably a di-C 12 ⁇ C 24 alkyl or alkenyl 'onion salt, especially a mono- or polyammonium salt, an imidazolinium salt or a mixture of such salts. Highly preferred are mono-quaternary ammonium salts, imidazolinium salts and mixtures thereof.
- the water-soluble cationic surfactant is preferably a mono-C 8 _ 24 alkyl or alkenyl 'onium salt, especially a mono- or polyammonium salt, an imidazolinium salt, a pyridinium salt or a mixture of such salts. Highly preferred are mono-quaternary ammonium salts, imidazolinium salts and mixtures thereof.
- the preferred water-soluble nonionic surfactant has the general formula RO(CH 2 CH 2 O) n H wherein R is a C 8 _ 20 alkyl or alkenyl group, and n is from 2 to 100.
- the weight ratio of water-insoluble cationic to water-soluble cationic and/or nonionic surfactant falls preferably in the range from 20:1 to 4:1, especially from 15:1 to 6:1.
- the weight ratio of the cationic softener to the hydrophobic adjunct preferably falls in the range from 8:1 to 2:1.
- compositions of the invention preferably comprise from 0.1 % to 6% of the water-soluble cationic and/or nonionic surfactant, from 0.5% to 6% of the non-cyclic hydrocarbon and from 0% to 6% of the fatty acid ester.
- percentage figures given for components in a composition refer to the weight percent of that component in the composition.
- highly preferred materials are C 12 ⁇ C 24 , especially C 12 ⁇ C 20 paraffins or paraffin mixtures, esters of C 12 ⁇ C 24 fatty acids with monohydric alcohols having from 1 to 8 carbon atoms, and mixtures of these paraffin and fatty acid ester materials in a 3:1 to 1:3 weight ratio.
- compositions of the invention thus comprise three essential ingredients, a water-insoluble cationic fabric softener, a water-soluble cationic and/or nonionic surfactant and a hydrophobic adjunct selected from C 10 ⁇ C 40 non-cyclic hydrocarbons and fatty acid ester, the water soluble surfactant and the hydrophobic adjunct acting in combination to provide compositions of optimum viscosity and stability.
- a water-insoluble cationic fabric softener e.g., a water-soluble cationic and/or nonionic surfactant and a hydrophobic adjunct selected from C 10 ⁇ C 40 non-cyclic hydrocarbons and fatty acid ester, the water soluble surfactant and the hydrophobic adjunct acting in combination to provide compositions of optimum viscosity and stability.
- a hydrophobic adjunct selected from C 10 ⁇ C 40 non-cyclic hydrocarbons and fatty acid ester
- the water-insoluble cationic fabric softener can be any fabric-substantive cationic compound which, in pure form as a strong acid salt (e.g. chloride), has a solubility in distilled water at pH 2.5 and 20°C of less than 1 g/I, or can be a mixture of such compounds.
- the soluble fraction of the surfactant is taken to be that material which cannot be separated from water by centrifugal action and which passes a 100 nm Nuclepore filter (Registered Trade Mark).
- Preferred materials are di-C 12 ⁇ C 24 alkyl or alkenyl 'onium salts, especially mono- and poly-ammonium salts, and imidazolinium salts.
- the two long chain alkyl or alkenyl groups may be substituted or interrupted by functional groups such as -OH, -0-, CONH-, -COO-, etc.
- substantially water-insoluble mono-ammonium compounds are the quaternary ammonium compounds having the formula:- wherein R, and R 2 represent alkyl or alkenyl groups of from 12 to 24 carbon atoms; R 3 and R 4 represent alkyl, alkenyl or hydroxyalkyl groups containing from 1 to 4 carbon atoms; and X is the salt counteranion, preferably selected from halide, methyl sulfate and ethyl sulfate radicals.
- these quaternary softeners include ditallow dimethyl ammonium chloride; ditallow dimethyl ammonium methyl sulfate; dihexadecyl dimethyl ammonium chloride; di(hydrogenated tallow alkyl) dimethyl ammonium chloride; dioctadecyl dimethyl ammonium chloride; dieicosyl dimethyl ammonium chloride; didocosyl dimethyl ammonium chloride di(hydrogenated tallow) dimethyl ammonium methyl sulfate; dihexadecyl diethyl ammonium chloride; di(coconut alkyl) dimethyl ammonium chloride and di(coconut alkyl) dimethyl ammonium methosulfate. Of these ditallow dimethyl ammonium chloride and di(hydrogenated tallow alkyl) dimethyl ammonium chloride are preferred.
- alkyl imidazolinium salts believed to have the formula:- wherein R s is an alkyl containing from 1 to 4, preferably 1 or 2 carbon atoms, R 7 is an alkyl containing from 12 to 24 carbon atoms, R ⁇ is an alkyl containing from 12 to 24 carbon atoms, and Rg is hydrogen or an alkyl containing from 1 to 4 carbon atoms and X is the salt counter-anion, preferably a halide, methosulfate or ethosulfate.
- Preferred imidazolinium salts include 3 - methyl - 1 - (tallowylamido)ethyl - 2 - tallowyl - 4,5 - dihydroimidazolinium methosulfate and 3 - methyl - 1 - (palmitoylamido)ethyl - 2 - octadecyl - 4,5 - dihydroimidazolinium chloride.
- imidazolinium materials are 2 - heptadecyl - 3 - methyl - 1 - (2 - stearylamido) - ethyl - 4,5 - dihydroimidazolinium chloride and 2 - lauryl - 3 - hydroxyethyl - 1 - (oleylamido)ethyl - 4,5 - dihydroimidazolinium chloride.
- the water-insoluble cationic softener is present at a level of at least 2%; below this level, the volume of product required to provide an acceptable level of softness benefit becomes excessively large.
- softener levels in the range of 2% to 6% there is, of course, generally no difficulty in preparing products of conventional type with the necessary low viscosity and good stability by adding, for instance, a low level of calcium chloride.
- product stability and viscosity become a problem and the overall aim is to adjust the levels of the softening and surfactant components within the prescribed limits to provide products which are stable to separation in a centrifuge at 3000 r.p.m.
- cationic softener in the present formulations is determined by practical considerations; thus, above a cationic softener level of 22% the problems of physical stability and product viscosity are such that it is not generally possible to formulate stable pourable emulsions based on water-insoluble cationic softener as the major softening component.
- the water-soluble surfactant is a cationic or nonionic surfactant having a solubility in distilled water at pH 2.5 and 20°C of greater than 1 g/I.
- solubility of the cationic surfactant is defined with reference to the pure material in the form of a strong acid salt (e.g. chloride), and the soluble fraction of the surfactant is taken to be that material which cannot be separated from water by centrifugal action and which passes a 100 nm Nuclepore filter.
- Preferred water-soluble cationic surfactants are mono-C 8 ⁇ C 24 alkyl or alkenyl ammonium salts, imidazolinium salts, pyridinium salts and mixtures thereof.
- Suitable water-soluble mono-ammonium compounds have the general formula: wherein R 5 represents a C 8 ⁇ C 24 alkyl or alkenyl group, R 6 represents hydrogen, a C 1 ⁇ C 12 alkyl, alkenyl or hydroxyalkyl group, an aryl group, a C 1 _ 6 alkylaryl group, or a poly(ethylene oxide) group having from 2 to 20 ethylene oxide units, R 7 , R 8 individually represent hydrogen, a C 1 ⁇ C 4 alkyl, alkenyl or hydroxyalkyl group or a poly(ethylene oxide) group having from 2 to 20 ethylene oxide units and X is as defined above.
- Highly preferred materials of this general type include the tallow trimethyl ammonium salts, cetyl trimethyl ammonium salts, myristyl trimethyl ammonium salts, coconutalkyl trimethyl ammonium salts, stearyl dimethyl ammonium salts, cetyl dimethyl ammonium salts, myristyl dimethyl ammonium salts, coconutalkyl dimethyl ammonium salts, oleyl methyl ammonium salts, palmityl methyl ammonium salts, myristyl methyl ammonium salts, lauryl methyl ammonium salts, dodecyl dimethyl hydroxyethyl ammonium salts, dodecyl dimethyl hydroxypropyl ammonium salts, myristyl dimethyl hydroxyethyl ammonium salts, dodecyl dimethyl dioxyethylenyl ammonium salts, myristyl benzyl hydroxyethyl methyl ammonium salts, coconutal
- Highly preferred water-soluble imidazolinium materials are represented by the general formula or acids salts thereof, wherein R 6 , R 7 , R 8 , Rg and X were defined earlier.
- Preferred imidazolinium salts of this general formula include the compound in which R s is methyl, R s is tallowyl and Rg is hydrogen and the compound in which R 6 is methyl, R 8 is palmitoyl and R 9 is hydrogen.
- Highly preferred water-soluble polyammonium cation materials are represented by the general formula: wherein R 11 is selected from an alkyl or alkenyl group having from 12 to 24, preferably from 16 to 20 carbon atoms in the alk(en)yl chain, R 11 CO ⁇ and R 11 ⁇ O ⁇ (CH 2 ) n ⁇ ; each R 10 is independently selected from hydrogen, ⁇ (C 2 H 4 O) p H, ⁇ (C 3 H 6 O) q H.
- Preferred water-soluble cationic materials are alkoxylated and contain not more than one -C 2 H 4 0H or -C 3 H B OH group attached to each nitrogen atom, except that up to two of these groups can be attached to a terminal nitrogen atom which is not substituted by an alkyl group having from 10 to 24 carbon atoms.
- Polyamine species suitable for use herein include:
- the water-soluble cationic surfactant herein can also be represented by alkyl pyridinium salts having the following formula: wherein R 12 is a C 10 ⁇ C 24 , preferably C 16 or C 18 alkyl radical and X is a suitable anion as defined hereinbefore, preferably a halide, especially chloride or bromide.
- water-soluble cationic surfactants of the amine-salt class can be added in the form of the neutral amine followed by pH adjustment to within the range from pH4 to pH8.
- the hydrophobic adjunct is selected from non-cyclic hydrocarbons, fatty acid esters of monohyáric alcohols and mixtures thereof, each component having a total of from 10 to 40 carbon atoms.
- the hydrophobic adjunct is present in an amount relative to the insoluble cationic softener and the water-soluble cationic and/or nonionic surfactant, to provide a dispersion of anisotropic softener phase in isotropic aqueous surfactant phase.
- the first class of hydrophobic adjunct is represented by non-cyclic hydrocarbons having from 10 to 40, preferably from 12 to 24, more preferably from 12 to 20 carbon atoms.
- hydrocarbons useful in the present invention are paraffins or olefins, but other materials, such as alkynes and halo-paraffins, for example myristyl chloride or stearyl bromide, are not excluded.
- Materials known generally as paraffin oil, soft paraffin wax and petrolatum are especially suitable. Examples of specific materials are tetradecane, hexadecane, octadecane and octadecene.
- Preferred commercially-available paraffin mixtures include spindle oil and light oil and technical grade mixtures of C 14 /C 17 and C 18 /C 20 n-paraffins.
- the second class of hydrophobic adjunct is represented by fatty acid esters having a total of 10 to 40 carbon atoms.
- Preferred materials are esters of C 8 ⁇ C 24 fatty acids with mono-hydric alcohols having from 1 to 8, especially from 1 to 4 carbon atoms.
- the mono-hydric alcohol portion of the ester can be represented by methanol, ethanol, n-propanol, iso-propanol, n-butanol, iso-butanol, t-butanol, 2-ethyl-hexanol and iso-octanol.
- Examples of such materials are methyl laurate, ethyl stearate, isopropyl myristate, isopropyl palmitate, iso-butyl stearate, isopropylstearate, 2-ethylhexyl laurate and isooctyl myristate.
- iso-butyl stearate is highly preferred.
- paraffins having from 12 to 20 carbon atoms constitute the preferred adjunct.
- mixtures of paraffins and fatty acid esters in a 3:1 to 1:3 weight ratio are also effective.
- the hydrophobic adjunct acts to lower the viscosity of the composition and because each of the materials has a long fatty chain, the agent does contribute to some extent to the softening performance of the composition, a feature which is not shared by other known viscosity control agents, for example electrolytes and low molecular weight solvent materials.
- Compositions of the present invention also have enhanced dispersibility in cold water and exhibit less dispenser residues than conventional fabric softening composition based solely on a cationic fabric softener.
- compositions may contain other textile treatment or conditioning agents.
- Such agents include silicones, as for example described in German Patent Application DOS 26 31 419 (DE-A-26 31 419).
- the optional silicone component can be used in an amount of from 0.1% to 6%, preferably from 0.5% to 2% of the softener composition.
- a further optional component of the present composition is a fatty acid ester of a polyhydric alcohol, for instance a C '2- C 22 fatty acid ester of ethylene glycol, propylene glycol, glycerol, diglycerol, xylitol, sucrose, erythritol, pentaerythritol, sorbitol or sorbitan.
- esters specific examples of which include ethyleneglycol monostearate, propyleneglycol monostearate, glyceryl monostearate and glyceryl distearate, can provide an additional softening facility.
- fatty acid esters are relatively hydrophilic and indeed are emulsifying materials in their own rights, it is desirable to include such materials in a level of no more than 4% by weight or in a weight ratio with respect to the cationic softener of no more than 2:3.
- compositions herein can contain other optional ingredients which are known to be suitable for use in textile softeners at usual levels for their known functions.
- adjuvants include emulsifiers, perfumes, preservatives, germicides, colorants, dyes fungicides, stabilizers, brighteners and opacifiers. These adjuvants, if used, are normally added at their conventional low levels.
- composition of the invention can also comprise additional viscosity control agents, such as 1% to 10% of lower alcohols, especially ethanol and isopropanol, and electrolytes, for example calcium chloride, at levels of from 100 to 1000 ppm. It is a feature of the invention, however, that such materials can be reduced or eliminated completely from the instant compositions.
- compositions can normally be prepared by mixing the ingredients together in water, heating to a temperature of about 60°C and agitating for 5-30 minutes.
- the pH of the compositions is generally adjusted to be in the range from 3 to 8, preferably from 4 to 6. In this preferred pH range, it will be understood that the neutralization of amines or polyamines in the composition can be incomplete.
- compositions of the present invention are added to the rinse liquor, a concentration from 10 ppm to 1000 ppm, preferably from 50 ppm to 500 ppm, of total active ingredient is appropriate.
- Concentrated liquid fabric softeners were prepared having the compositions indicated below, by dispersing the active ingredients in water at about 60°C.
- compositions had good phase stability, low viscosity, good dispersibility and excellent softening characteristics compared with compositions containing no hydrophobic adjunct or no water-soluble cationic or nonionic surfactants or with compositions in which the active system contains a major proportion of hydrophobic adjunct and/or soluble surfactant.
- Concentrated fabric softeners were prepared in analogous manner with the compositions indicated below.
- compositions were stable dispersions with low viscosity, good dispersibility and excellent softening characteristics compared with compositions containing no hydrophobic adjunct or soluble surfactant or with compositions in which the active system contains a major proportion of the hydrophobic adjunct and/or soluble surfactant.
- Aqueous fabric softening compositions were prepared according to the following formulae:-
- compositions were stable dispersions with low viscosity, good dispersibility and excellent softening characteristics compared with compositions containing no hydrophobic adjunct or soluble surfactant or with compositions in which the active system contains a major proportion of the hydrophobic adjunct and/or soluble surfactant.
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Abstract
Description
- This invention relates to fabric softening compositions and, in particular, to compositions in aqueous medium having improved softening effectiveness combined with excellent physical characteristics, especially formulation stability.
- Conventional rinse-added fabric softening compositions contain fabric softening agents which are substantially water-insoluble cationic materials usually having two long alkyl chains. Typical of such materials are distearyl di-methyl ammonium chloride and imidazolinium compounds substituted with two stearyl groups. These materials are normally prepared in the form of an aqueous dispersion or emulsion, and it is generally not possible to prepare such aqueous dispersions with more than about 6% of cationic material without taking special precautions to ensure acceptable viscosity and stability characteristics. Indeed, with cationic levels in excess of about 8% the problems of physical instability and high viscosity become, in the case of conventional fabric softening products, almost intractable. This, of course, limits the level of softening performance achievable with conventional compositions without using excessive amounts of product, and also adds substantially to distribution and packaging costs, because of the need to market such dilute solutions of the active ingredient.
- One approach which has been taken to improve the softening performance of cationic fabric softeners has been via the incorporatio.n of certain fatty or oily materials in the softener active system. While these adjunct materials have little intrinsic softening capability in their own right, they are apparently effective in extending the performance of conventional cationic softening materials, both in concentrated and normal softener compositions so that the cost-effectiveness of these compositions is considerably improved. Moreover, by incorporating relatively high proportions of the oily adjunct materials in relation to the cationic softener, and by adding thereto relatively high proportions of a water-soluble cationic surfactant in relation to the cationic. softener, concentrated softening compositions can be prepared containing a high total level of active softening materials. Reference is made to published European Patent Application No. 0000406 and Belgian Patent No. 868,934 (equivalent to DE-A1-2.830.173) both of which are relevant to this general approach.
- Formulations prepared in this manner, however, are still not entirely satisfactory. Thus, while such compositions do allow a high concentration of active ingredient, the level of softness benefit delivered by such compositions on a unit active weight basis is still much lower than for conventional dilute products and problems of physical formulation characteristics, especially phase stability and also viscosity, still remain. In particular, an important limitation of the prior art compositions is the difficulty in meeting simultaneous product stability and viscosity characteristics. Indeed, phase stability remains a problem even in the case of dilute softener compositions formulated in the manner of the above prior art references.
- Other approaches have also been taken for improving the physical characteristics of softener compositions of course. Thus, it is generally known (for example in U.S. Patent No. 3,681,241) that the presence of ionizable salts in concentrated compositions do help reduce viscosity, but these materials do not offer the additional benefit of enhancing the softening performance of the compositions. More importantly, the quantity of ionizable salts required for significant viscosity reduction is found to be generally deleterious in terms of product stability. Dutch patent application no. 6706178 (NL-A-6706178) relates to viscosity control in fabric softening compositions with up to 12% of cationic softener, and suggests the use of low molecular weight hydrocarbons for this purpose, while German patent application no. 25 03 026 (DE-A-2503026) discloses a complex softener/disinfec- tant composition in which a long chain fatty alcohol is suggested as a solubilization aid. Finally, U.S. Patent No. 3,793,196 describes an improved viscosity softening agent in the form of an oil-in- water emulsion comprising a cationic surface-active agent, a higher fatty alcohol, a sorbitan fatty acid ester and a polyethoxylated nonionic surfactant.
- The present invention accordingly provides a fabric softening composition having improved softening characteristics and cost-effectiveness combined with excellent physical characteristics, especially phase stability, freeze-thaw behaviour and low viscosity; and it further provides a concentrated fabric softening composition having satisfactory characteristics for consumer use, based on cationic fabric softener as the major active component.
- According to the present invention, there is provided an aqueous fabric softening composition characterized by:-
- (a) from 2% to 22% by weight of a water-insoluble cationic fabric softener,
- (b) from 0.05% to 8% by weight of a water-soluble cationic or nonionic surfactant or mixture thereof, and
- (c) from 0.25% to 15% by weight of a C10―C40 non-cyclic hydrocarbon, or of a fatty acid ester of a monohydric alcohol, said ester having a total of 10 to 40 carbon atoms, or of a mixture thereof,
- The physical form of the composition is that of a dispersion of an anisotropic softener phase in an aqueous isotropic surfactant solution phase. The physical form is simply determined under a polarizing microscope. The anisotropic/isotropic phase system is highly important for achieving optimum viscosity, stability, softening and other textile benefits.
- The water insoluble cationic fabric softener is preferably a di-C12―C24 alkyl or alkenyl 'onion salt, especially a mono- or polyammonium salt, an imidazolinium salt or a mixture of such salts. Highly preferred are mono-quaternary ammonium salts, imidazolinium salts and mixtures thereof.
- The water-soluble cationic surfactant is preferably a mono-C8_24 alkyl or alkenyl 'onium salt, especially a mono- or polyammonium salt, an imidazolinium salt, a pyridinium salt or a mixture of such salts. Highly preferred are mono-quaternary ammonium salts, imidazolinium salts and mixtures thereof.
- The preferred water-soluble nonionic surfactant has the general formula RO(CH2CH2O)nH wherein R is a C8_20 alkyl or alkenyl group, and n is from 2 to 100.
- From the point of view of optimum product stability and viscosity and softening performance, the weight ratio of water-insoluble cationic to water-soluble cationic and/or nonionic surfactant, falls preferably in the range from 20:1 to 4:1, especially from 15:1 to 6:1. The weight ratio of the cationic softener to the hydrophobic adjunct, on the other hand, preferably falls in the range from 8:1 to 2:1. In terms of level, compositions of the invention preferably comprise from 0.1 % to 6% of the water-soluble cationic and/or nonionic surfactant, from 0.5% to 6% of the non-cyclic hydrocarbon and from 0% to 6% of the fatty acid ester.
- In the present specification, percentage figures given for components in a composition refer to the weight percent of that component in the composition.
- With regard to the hydrophobic adjunct, highly preferred materials are C12―C24, especially C12―C20 paraffins or paraffin mixtures, esters of C12―C24 fatty acids with monohydric alcohols having from 1 to 8 carbon atoms, and mixtures of these paraffin and fatty acid ester materials in a 3:1 to 1:3 weight ratio.
- At lower concentrations of water-insoluble cationic softener, less than 6% by weight, it is preferred to include relatively low levels of water-soluble surfactant in relation to the insoluble softener for achieving optimum stability and viscosity, while at higher concentrations of water insoluble cationic softener, greater than 12% by weight, it is desirable to include relatively high levels of water-soluble surfactant in relation to the insoluble softener, Thus, there are three highly preferred executions:
- (A) A composition comprising:-
- (a) from 2% to 6% by weight of a water-insoluble di-C12―C24 alkyl or alkenyl mono-quaternary ammonium salt,
- (b) from 0.05 to 1% by weight of a water-soluble cationic surfactant which is:-
- (i) a mono-C8―C24 alkyl or alkenyl mono-quaternary salt,
- (ii) a mono-C8―C24 alkyl or alkenyl imidazolinium salt, or
- (iii) a mixture thereof, and
- (c) from 0.25% to 3% by weight of a C11―C24 paraffin or paraffin mixture, wherein the weight ratio of (a) to (b) is in the range from 20:1 to 4:1 and the weight ratio of (a) to (c) is in the range from 5:1 to 2:1.
- (B) A composition comprising:-
- (a) from 6% to 12% by weight of a water-insoluble cationic fabric softener which is a mixture of:-
- (i) a di-C12―C24 alkyl or alkenyl mono-quaternary ammonium salt, and
- (ii) a di-C12―C24 alkyl or alkenyl imidazolinium salt,
wherein the weight ratio of (i) to (ii) is in the range from 1:6 to 1:1,
- (b) from 0.5 to 6% by weight of a water-soluble cationic surfactant which is:-
- (i) a mono-C8―C24 alkyl or alkenyl mono-quaternary ammonium salt,
- (ii) a mono-C8―C24 alkyl or alkenyl imidazolinium salt, or
- (iii) a mixture thereof, and
- (c) from 1% to 6% by weight of a C12―C24 preferably C12―C20 paraffin or paraffin mixture, wherein the weight ratio of (a) to (b) is in the range from 10.1 to 5.2, and the weight ratio of (a) to (c) is in the range from 5:1 to 5:2; and
- (a) from 6% to 12% by weight of a water-insoluble cationic fabric softener which is a mixture of:-
- (C) A composition comprising
- (a) from 12% to 22% of a water-insoluble di-C12―C24 alkyl or alkenyl imidazolinium salt,
- (b) from 2% to 8% of a water-soluble cationic surfactant which is:-
- (i) a mono-C8―C24 alkyl or alkenyl mono-quaternary ammonium salt,
- (ii) a mono-C8―C24 alkyl or alkenyl imidazolinium salt, or
- (iii) a mixture thereof, and
- (c) from 6% to 12% of a 3:1 to 1:3 mixture of:-
- (i) a C12―C24 preferably C12―C30 paraffin or paraffin mixture, and
- (ii) an ester of a C12―C24 fatty acid with a C1―C8 monohydric alcohol. wherein the weight ratio of (a) to (b) is in the range from 4:1 to 5:2, and the weight ratio of (a) to (c) is in the range from 7:2 to 5:4.
- Compositions of the invention thus comprise three essential ingredients, a water-insoluble cationic fabric softener, a water-soluble cationic and/or nonionic surfactant and a hydrophobic adjunct selected from C10―C40 non-cyclic hydrocarbons and fatty acid ester, the water soluble surfactant and the hydrophobic adjunct acting in combination to provide compositions of optimum viscosity and stability. The essential components will now be discussed in detail.
- The water-insoluble cationic fabric softener can be any fabric-substantive cationic compound which, in pure form as a strong acid salt (e.g. chloride), has a solubility in distilled water at pH 2.5 and 20°C of less than 1 g/I, or can be a mixture of such compounds. In this context, the soluble fraction of the surfactant is taken to be that material which cannot be separated from water by centrifugal action and which passes a 100 nm Nuclepore filter (Registered Trade Mark). Preferred materials are di-C12―C24 alkyl or alkenyl 'onium salts, especially mono- and poly-ammonium salts, and imidazolinium salts. Optionally, the two long chain alkyl or alkenyl groups may be substituted or interrupted by functional groups such as -OH, -0-, CONH-, -COO-, etc.
- Well known species of substantially water-insoluble mono-ammonium compounds are the quaternary ammonium compounds having the formula:-
- Another preferred class of water-insoluble cationic materials are the alkyl imidazolinium salts believed to have the formula:-
- In the present invention, the water-insoluble cationic softener is present at a level of at least 2%; below this level, the volume of product required to provide an acceptable level of softness benefit becomes excessively large. For softener levels in the range of 2% to 6%, there is, of course, generally no difficulty in preparing products of conventional type with the necessary low viscosity and good stability by adding, for instance, a low level of calcium chloride. For corresponding products based on mixed cationic/hydrocarbon or ester softeners, however, product stability and viscosity become a problem and the overall aim is to adjust the levels of the softening and surfactant components within the prescribed limits to provide products which are stable to separation in a centrifuge at 3000 r.p.m. for 16 hours and which have a viscosity of less than 350 mPas, preferably less than 150 mPas measured in a Brookfield Viscometer, using Spindle No. 2 at 60 r.p.m. and at 21°C. The maximum level of cationic softener in the present formulations is determined by practical considerations; thus, above a cationic softener level of 22% the problems of physical stability and product viscosity are such that it is not generally possible to formulate stable pourable emulsions based on water-insoluble cationic softener as the major softening component.
- The water-soluble surfactant is a cationic or nonionic surfactant having a solubility in distilled water at pH 2.5 and 20°C of greater than 1 g/I. Once again, the solubility of the cationic surfactant is defined with reference to the pure material in the form of a strong acid salt (e.g. chloride), and the soluble fraction of the surfactant is taken to be that material which cannot be separated from water by centrifugal action and which passes a 100 nm Nuclepore filter.
- Preferred water-soluble cationic surfactants are mono-C8―C24 alkyl or alkenyl ammonium salts, imidazolinium salts, pyridinium salts and mixtures thereof.
- Suitable water-soluble mono-ammonium compounds have the general formula:
- Highly preferred materials of this general type include the tallow trimethyl ammonium salts, cetyl trimethyl ammonium salts, myristyl trimethyl ammonium salts, coconutalkyl trimethyl ammonium salts, stearyl dimethyl ammonium salts, cetyl dimethyl ammonium salts, myristyl dimethyl ammonium salts, coconutalkyl dimethyl ammonium salts, oleyl methyl ammonium salts, palmityl methyl ammonium salts, myristyl methyl ammonium salts, lauryl methyl ammonium salts, dodecyl dimethyl hydroxyethyl ammonium salts, dodecyl dimethyl hydroxypropyl ammonium salts, myristyl dimethyl hydroxyethyl ammonium salts, dodecyl dimethyl dioxyethylenyl ammonium salts, myristyl benzyl hydroxyethyl methyl ammonium salts, coconutalkyl benzyl hydroxyethyl methyl ammonium salts, dodecyl dihydroxyethyl methyl ammonium salts, cetyl dihydroxyethyl methyl ammonium salts, and stearyl dihydroxyethyl methyl ammonium salts.
- Highly preferred water-soluble imidazolinium materials are represented by the general formula
- Highly preferred water-soluble polyammonium cation materials are represented by the general formula:
- Preferred water-soluble cationic materials are alkoxylated and contain not more than one -C2H40H or -C3HBOH group attached to each nitrogen atom, except that up to two of these groups can be attached to a terminal nitrogen atom which is not substituted by an alkyl group having from 10 to 24 carbon atoms.
- Polyamine species suitable for use herein include:
- N-tallowyl,N,N',N'-tris(2-hydroxyethyl)1 ,3-propanediamine di-hydrochloride or dibenzoate;
- N-soybean alkyl 1,3-propane diammonium sulfate;
- N-stearyI,N,N'-di(2-hydroxyethyl)-N'-(3-hydroxypropyl)-1,3-propanediamine dihydrofluoride;
- N-cocoyl-N,N,N',N',N'-pentamethyl-1,3-propane diammonium dichloride or di-methosulfate;
- N-oleyl N,N',N'-tris (3-hydroxypropyl)-1,3-propanediamine dihydrofluoride;
- N-stearyl N,N',N'-tris(2-hydroxyethyl) N,N'-dimethy)-1,3-propanediammonium dimethylsulfate;
- N-palmityl N,N',N'-tris(3-hydroxypropyl)-1,3-propanediamine dihydrobromide;
- N-(stearyloxypropyl) N,N',N'-tris(3-hydroxypropyl)1,3-propanediammonium diacetate;
- N-tallowyl N-(3-aminopropyl)1,3-propanediamine trihydrochloride;
- N-oleyl N-[1N" N" bis(2-hydroxyethyl)3-aminopropyl]N',N'-bis(2-hydroxyethyl)1,3-diaminopropane tri- hydrofluoride;
- N-tallowyl diethylene triamine trihydrochloride.
-
- It should be understood, of course, that water-soluble cationic surfactants of the amine-salt class can be added in the form of the neutral amine followed by pH adjustment to within the range from pH4 to pH8.
- The hydrophobic adjunct is selected from non-cyclic hydrocarbons, fatty acid esters of monohyáric alcohols and mixtures thereof, each component having a total of from 10 to 40 carbon atoms. The hydrophobic adjunct is present in an amount relative to the insoluble cationic softener and the water-soluble cationic and/or nonionic surfactant, to provide a dispersion of anisotropic softener phase in isotropic aqueous surfactant phase.
- The first class of hydrophobic adjunct is represented by non-cyclic hydrocarbons having from 10 to 40, preferably from 12 to 24, more preferably from 12 to 20 carbon atoms.
- Preferably, hydrocarbons useful in the present invention are paraffins or olefins, but other materials, such as alkynes and halo-paraffins, for example myristyl chloride or stearyl bromide, are not excluded. Materials known generally as paraffin oil, soft paraffin wax and petrolatum are especially suitable. Examples of specific materials are tetradecane, hexadecane, octadecane and octadecene. Preferred commercially-available paraffin mixtures include spindle oil and light oil and technical grade mixtures of C14/C17 and C18/C20 n-paraffins.
- The second class of hydrophobic adjunct is represented by fatty acid esters having a total of 10 to 40 carbon atoms. Preferred materials are esters of C8―C24 fatty acids with mono-hydric alcohols having from 1 to 8, especially from 1 to 4 carbon atoms.
- The mono-hydric alcohol portion of the ester can be represented by methanol, ethanol, n-propanol, iso-propanol, n-butanol, iso-butanol, t-butanol, 2-ethyl-hexanol and iso-octanol.
- Examples of such materials are methyl laurate, ethyl stearate, isopropyl myristate, isopropyl palmitate, iso-butyl stearate, isopropylstearate, 2-ethylhexyl laurate and isooctyl myristate. Of the above, iso-butyl stearate is highly preferred.
- Of all the above, paraffins having from 12 to 20 carbon atoms constitute the preferred adjunct. However, mixtures of paraffins and fatty acid esters in a 3:1 to 1:3 weight ratio are also effective.
- Apart from enhancing the phase stability of the composition, the hydrophobic adjunct acts to lower the viscosity of the composition and because each of the materials has a long fatty chain, the agent does contribute to some extent to the softening performance of the composition, a feature which is not shared by other known viscosity control agents, for example electrolytes and low molecular weight solvent materials. Compositions of the present invention also have enhanced dispersibility in cold water and exhibit less dispenser residues than conventional fabric softening composition based solely on a cationic fabric softener.
- In addition to the above-mentioned components, the compositions may contain other textile treatment or conditioning agents. Such agents include silicones, as for example described in German Patent Application DOS 26 31 419 (DE-A-26 31 419).
- The optional silicone component can be used in an amount of from 0.1% to 6%, preferably from 0.5% to 2% of the softener composition.
- A further optional component of the present composition is a fatty acid ester of a polyhydric alcohol, for instance a C'2-C22 fatty acid ester of ethylene glycol, propylene glycol, glycerol, diglycerol, xylitol, sucrose, erythritol, pentaerythritol, sorbitol or sorbitan. These esters, specific examples of which include ethyleneglycol monostearate, propyleneglycol monostearate, glyceryl monostearate and glyceryl distearate, can provide an additional softening facility. However, in as much as such fatty acid esters are relatively hydrophilic and indeed are emulsifying materials in their own rights, it is desirable to include such materials in a level of no more than 4% by weight or in a weight ratio with respect to the cationic softener of no more than 2:3.
- The compositions herein can contain other optional ingredients which are known to be suitable for use in textile softeners at usual levels for their known functions. Such adjuvants include emulsifiers, perfumes, preservatives, germicides, colorants, dyes fungicides, stabilizers, brighteners and opacifiers. These adjuvants, if used, are normally added at their conventional low levels.
- The composition of the invention can also comprise additional viscosity control agents, such as 1% to 10% of lower alcohols, especially ethanol and isopropanol, and electrolytes, for example calcium chloride, at levels of from 100 to 1000 ppm. It is a feature of the invention, however, that such materials can be reduced or eliminated completely from the instant compositions.
- The compositions can normally be prepared by mixing the ingredients together in water, heating to a temperature of about 60°C and agitating for 5-30 minutes.
- The pH of the compositions is generally adjusted to be in the range from 3 to 8, preferably from 4 to 6. In this preferred pH range, it will be understood that the neutralization of amines or polyamines in the composition can be incomplete.
- When compositions of the present invention are added to the rinse liquor, a concentration from 10 ppm to 1000 ppm, preferably from 50 ppm to 500 ppm, of total active ingredient is appropriate.
-
-
- The above compositions had good phase stability, low viscosity, good dispersibility and excellent softening characteristics compared with compositions containing no hydrophobic adjunct or no water-soluble cationic or nonionic surfactants or with compositions in which the active system contains a major proportion of hydrophobic adjunct and/or soluble surfactant.
-
- The above compositions were stable dispersions with low viscosity, good dispersibility and excellent softening characteristics compared with compositions containing no hydrophobic adjunct or soluble surfactant or with compositions in which the active system contains a major proportion of the hydrophobic adjunct and/or soluble surfactant.
-
- The above compositions were stable dispersions with low viscosity, good dispersibility and excellent softening characteristics compared with compositions containing no hydrophobic adjunct or soluble surfactant or with compositions in which the active system contains a major proportion of the hydrophobic adjunct and/or soluble surfactant.
wherein the weight ratio of (a) to (b) is in the range from 100:1 to 5:2, and the weight ratio of (a) to (c) is in the range from 20:1 to 5:4.
Claims (10)
wherein the weight ratio of (a) to (b) is in the range from 10:1 to 5:2, and the weight ratio of (a) to (c) is in the range from 5:1 to 5:2.
wherein the weight ratio of (a) to (b) is in the range from 4:1 to 5:2, and the weight ratio of (a) to (c) is in the range from 7:2 to 5:4.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT80200320T ATE6524T1 (en) | 1979-04-21 | 1980-04-10 | FABRIC SOFTENER COMPOSITION. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7913934 | 1979-04-21 | ||
GB7913934 | 1979-04-21 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0018039A1 EP0018039A1 (en) | 1980-10-29 |
EP0018039B1 true EP0018039B1 (en) | 1984-03-07 |
EP0018039B2 EP0018039B2 (en) | 1988-08-24 |
Family
ID=10504691
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP80200320A Expired EP0018039B2 (en) | 1979-04-21 | 1980-04-10 | Fabric softening composition |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0018039B2 (en) |
JP (1) | JPS569477A (en) |
AT (1) | ATE6524T1 (en) |
CA (1) | CA1154206A (en) |
DE (1) | DE3066798D1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9150822B2 (en) | 2010-12-03 | 2015-10-06 | Conopco, Inc. | Fabric conditioners |
Families Citing this family (53)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0032267A1 (en) * | 1980-01-11 | 1981-07-22 | THE PROCTER & GAMBLE COMPANY | Concentrated textile treatment compositions and method for preparing them |
US4395342A (en) * | 1980-06-06 | 1983-07-26 | The Procter & Gamble Company | Granular fabric softening composition |
ATE13562T1 (en) * | 1981-01-16 | 1985-06-15 | Procter & Gamble | TEXTILE TREATMENT AGENTS. |
EP0059502B1 (en) * | 1981-02-28 | 1985-06-26 | THE PROCTER & GAMBLE COMPANY | Textile treatment compositions |
DE3271812D1 (en) * | 1981-03-07 | 1986-07-31 | Procter & Gamble | Textile treatment compositions and preparation thereof |
US4464271A (en) * | 1981-08-20 | 1984-08-07 | International Flavors & Fragrances Inc. | Liquid or solid fabric softener composition comprising microencapsulated fragrance suspension and process for preparing same |
US4446032A (en) * | 1981-08-20 | 1984-05-01 | International Flavors & Fragrances Inc. | Liquid or solid fabric softener composition comprising microencapsulated fragrance suspension and process for preparing same |
DE3138181A1 (en) * | 1981-09-25 | 1983-04-14 | Bayer Ag, 5090 Leverkusen | TEXTILE TREATMENT AGENTS AND THEIR USE FOR FINISHING TEXTILE MATERIALS |
US4445901A (en) * | 1981-10-09 | 1984-05-01 | Lever Brothers Company | Fabric conditioning composition |
US4454049A (en) * | 1981-11-14 | 1984-06-12 | The Procter & Gamble Company | Textile treatment compositions |
US4439335A (en) * | 1981-11-17 | 1984-03-27 | The Procter & Gamble Company | Concentrated fabric softening compositions |
DE3150179A1 (en) * | 1981-12-18 | 1983-06-23 | Hoechst Ag, 6230 Frankfurt | CONCENTRATED PRE-MIXTURES OF SOFT SOFTENER |
DE3204165A1 (en) * | 1982-02-06 | 1983-08-11 | Hoechst Ag, 6230 Frankfurt | CONCENTRATED SOFT SOFTENER |
US4464273A (en) | 1982-02-10 | 1984-08-07 | Lever Brothers Company | Fabric softening composition |
US4464272A (en) | 1982-02-10 | 1984-08-07 | Lever Brothers Company | Fabric softening composition |
US4442013A (en) * | 1982-03-22 | 1984-04-10 | Colgate-Palmolive Company | Concentrated fabric softening compositions |
US4497716A (en) * | 1982-12-23 | 1985-02-05 | Lever Brothers Company | Fabric softening composition |
FR2540901B1 (en) * | 1983-02-14 | 1986-08-29 | Elf Aquitaine | CONCENTRATED COMPOSITIONS OF TEXTILE SOFTENERS |
US4808321A (en) * | 1987-05-01 | 1989-02-28 | The Procter & Gamble Company | Mono-esters as fiber and fabric treatment compositions |
EP0293955B1 (en) | 1987-05-01 | 1993-01-13 | The Procter & Gamble Company | Quaternary isopropyl ester ammonium compounds as fiber and fabric treatment compositions |
EP0294893A3 (en) * | 1987-06-10 | 1989-11-02 | The Procter & Gamble Company | Conditioning agents and compositions containing same |
US4913828A (en) * | 1987-06-10 | 1990-04-03 | The Procter & Gamble Company | Conditioning agents and compositions containing same |
US4789491A (en) * | 1987-08-07 | 1988-12-06 | The Procter & Gamble Company | Method for preparing biodegradable fabric softening compositions |
US4851139A (en) * | 1987-08-26 | 1989-07-25 | The Clorox Company | Isotropic fabric softener composition containing fabric mildewstat |
EP0309052B1 (en) * | 1987-09-23 | 1992-11-25 | The Procter & Gamble Company | Stable biodegradable fabric softening compositions containing linear alkoxylated alcohols |
EP0316996A3 (en) * | 1987-11-18 | 1990-04-04 | The Procter & Gamble Company | Method for preparing textile treatment compositions |
US4840738A (en) * | 1988-02-25 | 1989-06-20 | The Procter & Gamble Company | Stable biodegradable fabric softening compositions containing 2-hydroxypropyl monoester quaternized ammonium salts |
GB8827697D0 (en) * | 1988-11-28 | 1988-12-29 | Unilever Plc | Fabric-treatment composition |
GB8827698D0 (en) * | 1988-11-28 | 1988-12-29 | Unilever Plc | Fabric-treatment composition |
US5116520A (en) * | 1989-09-06 | 1992-05-26 | The Procter & Gamble Co. | Fabric softening and anti-static compositions containing a quaternized di-substituted imidazoline ester fabric softening compound with a nonionic fabric softening compound |
FR2655658B1 (en) * | 1989-12-08 | 1994-11-18 | Rhone Poulenc Chimie | LAUNDRY COMPOUND BASED ON A POLYPHOSPHATE AND IN PARTICULAR AN OPTICALLY ACTIVE AGENT, ITS PREPARATION METHOD AND ITS USE IN DETERGENCE. |
GB9011785D0 (en) * | 1990-05-25 | 1990-07-18 | Unilever Plc | Fabric treatment compositions |
ATE212658T1 (en) * | 1995-08-31 | 2002-02-15 | Colgate Palmolive Co | STABLE FABRIC SOFTENER COMPOSITIONS |
WO2000055286A2 (en) * | 1999-03-18 | 2000-09-21 | Mark Gary Mullane | Cleaning formulation |
GB0014891D0 (en) † | 2000-06-16 | 2000-08-09 | Unilever Plc | Fabric softening compositions |
CN100345953C (en) * | 2001-03-07 | 2007-10-31 | 宝洁公司 | Rinse-added fabric conditioning composition for use where residual detergent is present |
US8242071B2 (en) | 2006-10-06 | 2012-08-14 | Dow Corning Corporation | Process for preparing fabric softener compositions |
EP2053119B1 (en) * | 2007-10-26 | 2016-09-07 | The Procter and Gamble Company | Fabric softening compositions having improved stability upon storage |
JP5610964B2 (en) * | 2010-10-07 | 2014-10-22 | ライオン株式会社 | Liquid softener composition |
MX342414B (en) | 2010-10-22 | 2016-09-28 | Unilever Nv | Improvements relating to fabric conditioners. |
US10017715B2 (en) | 2013-02-15 | 2018-07-10 | Rhodia Operations | Fabric softener |
WO2014154234A1 (en) | 2013-03-25 | 2014-10-02 | Rhodia Operations | Fabric softener |
CN105793405A (en) * | 2013-10-10 | 2016-07-20 | 阿克苏诺贝尔化学品国际有限公司 | Fabric softener composition and the use thereof |
WO2015074692A1 (en) | 2013-11-20 | 2015-05-28 | Rhodia Operations | Fabric softener composition |
KR102254359B1 (en) | 2014-06-18 | 2021-05-24 | 로디아 오퍼레이션스 | Composition comprising a quaternary ammonium compound, a cationic polysaccharide and a nonionic polysaccharide |
KR102457934B1 (en) | 2015-01-16 | 2022-10-24 | 로디아 오퍼레이션스 | How to reduce graying of fabrics |
WO2016120291A1 (en) | 2015-01-28 | 2016-08-04 | Rhodia Operations | Composition containing ester quat, cationic polysaccharide and nonionic polysaccharide |
WO2016135217A1 (en) | 2015-02-27 | 2016-09-01 | Rhodia Operations | Composition comprising a quaternary ammonium compound, a cationic polysaccharide and a nonionic polymer |
WO2017100992A1 (en) | 2015-12-15 | 2017-06-22 | Rhodia Operations | Compositions comprising quat and polysaccharides |
US10351805B2 (en) | 2015-12-22 | 2019-07-16 | Rhodia Operations | Compositions comprising a quat and a mixture of a nonionic and two cationic polysaccharides |
AU2015419145B2 (en) | 2015-12-28 | 2018-09-13 | Colgate-Palmolive Company | Fabric softening compositions |
US20220403293A1 (en) | 2019-10-03 | 2022-12-22 | Rhodia Operations | Polymer dispersion and a fabric conditioning composition comprising the same |
WO2021063779A1 (en) | 2019-10-03 | 2021-04-08 | Rhodia Operations | Fabric conditioning composition comprising polymer dispersion |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5120638B1 (en) * | 1971-03-31 | 1976-06-26 | ||
US3974076A (en) * | 1974-01-11 | 1976-08-10 | The Procter & Gamble Company | Fabric softener |
DE2631114C3 (en) * | 1975-07-14 | 1981-11-26 | The Procter & Gamble Co., 45202 Cincinnati, Ohio | Fabric softeners |
DE2733493C2 (en) * | 1976-05-17 | 1986-11-13 | Henkel KGaA, 4000 Düsseldorf | Smoothing agent for textile fiber material |
US4155855A (en) * | 1977-07-06 | 1979-05-22 | The Procter & Gamble Company | Concentrated liquid fabric softener composition |
GB1601360A (en) * | 1977-07-12 | 1981-10-28 | Procter & Gamble | Textile treatment composition |
-
1980
- 1980-04-10 DE DE8080200320T patent/DE3066798D1/en not_active Expired
- 1980-04-10 EP EP80200320A patent/EP0018039B2/en not_active Expired
- 1980-04-10 AT AT80200320T patent/ATE6524T1/en not_active IP Right Cessation
- 1980-04-18 CA CA000350155A patent/CA1154206A/en not_active Expired
- 1980-04-21 JP JP5278180A patent/JPS569477A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9150822B2 (en) | 2010-12-03 | 2015-10-06 | Conopco, Inc. | Fabric conditioners |
Also Published As
Publication number | Publication date |
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ATE6524T1 (en) | 1984-03-15 |
CA1154206A (en) | 1983-09-27 |
DE3066798D1 (en) | 1984-04-12 |
EP0018039B2 (en) | 1988-08-24 |
JPS569477A (en) | 1981-01-30 |
EP0018039A1 (en) | 1980-10-29 |
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