CA1192003A - Fabric softening composition - Google Patents
Fabric softening compositionInfo
- Publication number
- CA1192003A CA1192003A CA000420859A CA420859A CA1192003A CA 1192003 A CA1192003 A CA 1192003A CA 000420859 A CA000420859 A CA 000420859A CA 420859 A CA420859 A CA 420859A CA 1192003 A CA1192003 A CA 1192003A
- Authority
- CA
- Canada
- Prior art keywords
- lanolin
- fabric softening
- composition
- cationic
- 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
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 63
- 239000004744 fabric Substances 0.000 title claims abstract description 56
- 239000004166 Lanolin Substances 0.000 claims abstract description 48
- 235000019388 lanolin Nutrition 0.000 claims abstract description 48
- 229940039717 lanolin Drugs 0.000 claims abstract description 45
- 239000000463 material Substances 0.000 claims abstract description 29
- 239000004902 Softening Agent Substances 0.000 claims description 26
- 125000002091 cationic group Chemical group 0.000 claims description 26
- 239000004615 ingredient Substances 0.000 abstract description 12
- 239000000470 constituent Substances 0.000 abstract description 9
- 239000004665 cationic fabric softener Substances 0.000 abstract description 2
- 239000002752 cationic softener Substances 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- -1 terpene alcohols Chemical class 0.000 description 13
- 235000014113 dietary fatty acids Nutrition 0.000 description 12
- 239000000194 fatty acid Substances 0.000 description 12
- 229930195729 fatty acid Natural products 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 150000002148 esters Chemical class 0.000 description 9
- 150000001298 alcohols Chemical class 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- 229920001223 polyethylene glycol Polymers 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 239000002202 Polyethylene glycol Substances 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 4
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 239000001110 calcium chloride Substances 0.000 description 4
- 229910001628 calcium chloride Inorganic materials 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
- 239000003792 electrolyte Substances 0.000 description 4
- 125000005456 glyceride group Chemical group 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- RZJRJXONCZWCBN-UHFFFAOYSA-N octadecane Chemical compound CCCCCCCCCCCCCCCCCC RZJRJXONCZWCBN-UHFFFAOYSA-N 0.000 description 4
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 101100102380 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) vma-1 gene Proteins 0.000 description 3
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- QYIXCDOBOSTCEI-QCYZZNICSA-N (5alpha)-cholestan-3beta-ol Chemical compound C([C@@H]1CC2)[C@@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@H](C)CCCC(C)C)[C@@]2(C)CC1 QYIXCDOBOSTCEI-QCYZZNICSA-N 0.000 description 2
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 2
- YQEMORVAKMFKLG-UHFFFAOYSA-N 2-stearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 2
- FLIACVVOZYBSBS-UHFFFAOYSA-N Methyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC FLIACVVOZYBSBS-UHFFFAOYSA-N 0.000 description 2
- 101100049019 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) vma-6 gene Proteins 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 229930182558 Sterol Natural products 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- QYIXCDOBOSTCEI-UHFFFAOYSA-N alpha-cholestanol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)CCCC(C)C)C1(C)CC2 QYIXCDOBOSTCEI-UHFFFAOYSA-N 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical group 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 235000012000 cholesterol Nutrition 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- MMKRHZKQPFCLLS-UHFFFAOYSA-N ethyl myristate Chemical compound CCCCCCCCCCCCCC(=O)OCC MMKRHZKQPFCLLS-UHFFFAOYSA-N 0.000 description 2
- MVLVMROFTAUDAG-UHFFFAOYSA-N ethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC MVLVMROFTAUDAG-UHFFFAOYSA-N 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- CBFCDTFDPHXCNY-UHFFFAOYSA-N icosane Chemical compound CCCCCCCCCCCCCCCCCCCC CBFCDTFDPHXCNY-UHFFFAOYSA-N 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- AOHAPDDBNAPPIN-UHFFFAOYSA-N myristicinic acid Natural products COC1=CC(C(O)=O)=CC2=C1OCO2 AOHAPDDBNAPPIN-UHFFFAOYSA-N 0.000 description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 229940038384 octadecane Drugs 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- REIUXOLGHVXAEO-UHFFFAOYSA-N pentadecan-1-ol Chemical compound CCCCCCCCCCCCCCCO REIUXOLGHVXAEO-UHFFFAOYSA-N 0.000 description 2
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 150000003432 sterols Chemical class 0.000 description 2
- 235000003702 sterols Nutrition 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 2
- 239000004034 viscosity adjusting agent Substances 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- ZBFPGLKEWSMWSG-BQNIITSRSA-N (3S,5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-3-ol Chemical compound CC1(C)[C@@H](O)CC[C@]2(C)C3=CC[C@]4(C)[C@@H]([C@@H](CCC=C(C)C)C)CC[C@@]4(C)C3=CC[C@H]21 ZBFPGLKEWSMWSG-BQNIITSRSA-N 0.000 description 1
- ZCBDFGFNCFLBOL-BQNIITSRSA-N (3S,5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-3-ol Chemical compound CC1(C)[C@@H](O)CC[C@]2(C)C3=CC[C@]4(C)[C@@H]([C@H](C)CCCC(C)C)CC[C@@]4(C)C3=CC[C@H]21 ZCBDFGFNCFLBOL-BQNIITSRSA-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
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 1
- JNSSVMGPTZYYIW-UHFFFAOYSA-N 2-chloro-6-methyl-1-oxidopyridin-1-ium Chemical compound CC1=CC=CC(Cl)=[N+]1[O-] JNSSVMGPTZYYIW-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
- XMMODWGMKHUZQW-UHFFFAOYSA-N 2-hydroxy-16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCC(O)C(O)=O XMMODWGMKHUZQW-UHFFFAOYSA-N 0.000 description 1
- ZBNVMPVEBXTLJF-UHFFFAOYSA-N 24-methylhexacosan-1-ol Chemical compound CCC(C)CCCCCCCCCCCCCCCCCCCCCCCO ZBNVMPVEBXTLJF-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
- 239000005711 Benzoic acid Substances 0.000 description 1
- 101100065885 Caenorhabditis elegans sec-15 gene Proteins 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 102000005575 Cellulases Human genes 0.000 description 1
- 108010084185 Cellulases Proteins 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- UCTLRSWJYQTBFZ-UHFFFAOYSA-N Dehydrocholesterol Natural products C1C(O)CCC2(C)C(CCC3(C(C(C)CCCC(C)C)CCC33)C)C3=CC=C21 UCTLRSWJYQTBFZ-UHFFFAOYSA-N 0.000 description 1
- 229920002307 Dextran Polymers 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 101100372584 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) vma-3 gene Proteins 0.000 description 1
- 101100209646 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) vma-4 gene Proteins 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 206010040914 Skin reaction Diseases 0.000 description 1
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical group CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
- IJCWFDPJFXGQBN-RYNSOKOISA-N [(2R)-2-[(2R,3R,4S)-4-hydroxy-3-octadecanoyloxyoxolan-2-yl]-2-octadecanoyloxyethyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCCCCCCCCCCCC IJCWFDPJFXGQBN-RYNSOKOISA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- ZBFPGLKEWSMWSG-UHFFFAOYSA-N agnosterone Natural products CC1(C)C(O)CCC2(C)C3=CCC4(C)C(C(CCC=C(C)C)C)CCC4(C)C3=CCC21 ZBFPGLKEWSMWSG-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000001345 alkine derivatives Chemical class 0.000 description 1
- 159000000013 aluminium salts Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N beta-monoglyceryl stearate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 238000009530 blood pressure measurement Methods 0.000 description 1
- 239000006172 buffering agent Substances 0.000 description 1
- RICLFGYGYQXUFH-UHFFFAOYSA-N buspirone hydrochloride Chemical compound [H+].[Cl-].C1C(=O)N(CCCCN2CCN(CC2)C=2N=CC=CN=2)C(=O)CC21CCCC2 RICLFGYGYQXUFH-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229940037395 electrolytes Drugs 0.000 description 1
- 229910001651 emery Inorganic materials 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229940093476 ethylene glycol Drugs 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- ZCBDFGFNCFLBOL-UHFFFAOYSA-N gamma-Lanostadienol Natural products CC1(C)C(O)CCC2(C)C3=CCC4(C)C(C(C)CCCC(C)C)CCC4(C)C3=CCC21 ZCBDFGFNCFLBOL-UHFFFAOYSA-N 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- 150000002398 hexadecan-1-ols Chemical class 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 229920000831 ionic polymer Polymers 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 229940037626 isobutyl stearate Drugs 0.000 description 1
- OAOABCKPVCUNKO-UHFFFAOYSA-N isodecanoic acid Natural products CC(C)CCCCCCC(O)=O OAOABCKPVCUNKO-UHFFFAOYSA-N 0.000 description 1
- 229940089456 isopropyl stearate Drugs 0.000 description 1
- 229940099367 lanolin alcohols Drugs 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- CPXCDEMFNPKOEF-UHFFFAOYSA-N methyl 3-methylbenzoate Chemical compound COC(=O)C1=CC=CC(C)=C1 CPXCDEMFNPKOEF-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229940068917 polyethylene glycols Drugs 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 239000002243 precursor 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
- 238000000746 purification Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 230000035483 skin reaction Effects 0.000 description 1
- 231100000430 skin reaction Toxicity 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- RBWSWDPRDBEWCR-RKJRWTFHSA-N sodium;(2r)-2-[(2r)-3,4-dihydroxy-5-oxo-2h-furan-2-yl]-2-hydroxyethanolate Chemical compound [Na+].[O-]C[C@@H](O)[C@H]1OC(=O)C(O)=C1O RBWSWDPRDBEWCR-RKJRWTFHSA-N 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 239000001589 sorbitan tristearate Substances 0.000 description 1
- 235000011078 sorbitan tristearate Nutrition 0.000 description 1
- 229960004129 sorbitan tristearate Drugs 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- QYSXJUFSXHHAJI-YRZJJWOYSA-N vitamin D3 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-YRZJJWOYSA-N 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/384—Animal products
-
- 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
- C11D3/0005—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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
ABSTRACT:
A fabric softening composition comprises an aqueous base, a cationic fabric softener and up to about 10%
lanolin. The cationic softener and lanolin are preferably in the ratio of 20:1 to 1:20 and the level of cationic softener in the composition may be from 0.5% to 30%.
Other conventional fabric softening composition ingredients may be present. The lanolin may be replaced by a lanolin-like material such as derivatives thereof or one or more of the active constituents of lanolin either extracted therefrom or derived from other sources. The presence of lanolin in the composition improves the viscosity and performance thereof.
A fabric softening composition comprises an aqueous base, a cationic fabric softener and up to about 10%
lanolin. The cationic softener and lanolin are preferably in the ratio of 20:1 to 1:20 and the level of cationic softener in the composition may be from 0.5% to 30%.
Other conventional fabric softening composition ingredients may be present. The lanolin may be replaced by a lanolin-like material such as derivatives thereof or one or more of the active constituents of lanolin either extracted therefrom or derived from other sources. The presence of lanolin in the composition improves the viscosity and performance thereof.
Description
Z~1~3 FABRIC SOFTENING COMPOSITION
_ FIELD OF THE INVE~ION
,.. . .
The present invention relates to a fabric softening composition. In particular, but not exclusively, it 5 relates to an aqueous based concentrated fabric softening composition.
BACKGROUND ART
It is known to treat fabrics, particularly after washing, with fabric softening agents in order to improve the feel of the fabrics and, in the case of clothes, to improve the comfort in wear. Traditionally, fabric softening agents are applied from an aqueous liquor which 15 is made up by adding a relatively small volume of a fabric soEtening composition to a large volume of water, for example during the rinse cycle in an automatic washing machine. The fabric softening composition is usually an aqueous liquid product containing less than ahout 8~ of a 20 cationic fabric softening agent. For a number of reasons, including or example the cost of packaging, it would be preferred if the product were to contain more than 8% of the active ingredient but due to difficulties in 3~
manufacture, storage and ease of use of the products, it has only been possible to do this in the past with some difficulty.
Further, there may be a desire to partially replace the cationic fabric softening agent with a material which is less costly, easier to handle or less prone to causing skin reaction w~-ile at the same time maintaining or substantially maintaining the performance of the productO
As set out in more detail below, the present invention seeks to overcome one or more of the objectives referred to above by the combined use of a cationic fabric softening agent and lanolin or a lanolin-like material.
SUMM~RY OF TH~ INVENTION
According to the invention there is provided a fabric softening composition comprising an aqueous base and at least 0.5~ by weight of a cationic fabric softening agent, characterised in that it further comprises from 0.25% up to 10% by weight of lanolin or a lanolin-like material.
An essential component of the present invention is lanolin or a lanolin-like material. Lanolin is wool wax which has been purified by various purification steps including washing, neutralisation, filtration, bleaching and deodorisation. Lanolin is composed primarily of esters which constitute the active constituents in the present invention and which yield on hydrolysis a mixture of complex alcohols and fatty acids. The alcohols which form about half of the ester component by weight, include sterols and terpene alcohols. The sterols amount to about 30% and include cholesterol, 7-dehydrocholesterol and cerebosterol and dihydrocholesterol (cholestanol). The terpene alcohols include lanesterol (C30H50O), dih~drlaneSterl (C30H52)' agnosterol (C30H48o)~
dihydroagnosterol (C30H500).
Lanolin is available commercially in a number of forms. Lanolin as such contains the active constituents primarily in their ester form. It is also available in two hydrolysed forms where the active constituents are primarily in their alcoholic or carboxylic acid form.
Further, lanolin may be hydrogenated to form a product where the active constituents are present primarily only in their alcoholic form. Lanolin is also commercially available in propo~ylated and acetylated forms. As used herein the term "lanolin" is intended to refer to any such material derived from wool wax whether the active constituents are in the alco~olic, ester, alkoxylated, hydrogenated or other chemical form.
Suitable commercial forms of lanolin include Corona (lanolin BP~, ~artolan, Polychol and Coronet (Trade Marks of Croda Chemicals Ltd), Solulan, Acetulan and Modulan (Trade Marks of American Cholesterol Products Inc) and Lanocerina ~Trade Mark - Esperis SpA Milan). Commercial lanolin is also available from Westbrook Lanolin Co., Bradford, England.
Many of the active constituents of lanolin can be prepared synthetically, from sources other than wool WAX
or can be ~xtracted from wool wax and other naturally occurring material~. While for cost reasons the commercially available forms of lanolin are preferred for the present invention, it is also possible to use any one or more of the active constituents referred to above however derived, and also materials of similar structure.
Thu , in place of lanolin one may use a "lanolin-like material" which term as used herein includes ~2~
ta) any Ol~ or more of the active lanolin constituents ref~ .o above, and the carboxylic acid or alcohol, derivatives thereof;
5 (b) the corresponding carboxylic acids or alcohols and ester derivatives of the material~ listed in (a), in particular the esters thereof with fatty acids or alcohols containing at least 12 carbon atoms.
10 ~c) iso- and anteiso- alcohols and acids and derivatives thereof having the general formula CH- Rl -X
where Rl is a divalent straight or branched chain, saturated or unsaturated, substituted or unsubstituted hydrocarbyl group having at least 7, preferably at least 15 carbon atoms, R2 is a methyl or ethyl group and X is OH, -COOH, -O -C -R or ~COOR ~here R is a hydrocarhyl group, in particular a fatty acid alkyl group containing of at least 12 carbon atoms. Examples of materials in this group include 16-methyl heptadecanol, 24-methyl hexacosanol, 8-methyl nonanoic acid: and 2-hydroxy-16-methyl heptadecanoic acid.
The level of lanolin or lanolin-like material in the fabric softening compositions is from 0.25% up to 10% by weight, such as between 0.5% and 5% by weight of the 35 composition.
3~ a3 Any well-known cationic fabric softening agent can be used in the present invention, as well as mixtures of two or more of such agents.
Suitable e~amples of cat.ionic fabric-softening agents are quaternary ammonium compounds containing two long alkyl or alkenyl chains with 12-22 carbon atoms such as di(hardened or unhardened tallow) dimethyl ammonium-chloride~ 2-heptadecyl-2methylstearoyl amido ethyl imida~oline methosulphate, di-(coco)dimethyl ammoni.um-chloride, etc. These cationic fabric-softening agents are well-known in the art and furthex suitable examples can be found in Schwartz-Perry. "Surface-actiYe Agents and Detergents" Yol II, 1958.
~5 Relatively water-soluble cationic softening agents, such as the monoalkyl quaternary ammonium compounds s~ch as stearyltrimethylammoniumchloride, may also be used, but, as they are often less effective softeners, they are preferably used in conjunction with other, more effective cationic fabric softening agents or witi, llu,~ Lionic softening agents such as fatty acid esters of polyols such as sorbitantristearate, glycerolmonostearate, and so on, or with anîonic detergents with which they are capable of forming softening compl.exes, such as fatty acid soaps.
They may also be made more hydrophobic by treatment with suitable hydrophobising agents such as long chain alcohols and fatty acids. The present invention is however of particular benefit if the more effective, less water-soluble cationic softening agents having two long alkylchains are used.
The level of cationic fabric softening agent in the aqueous fabric softening compositions is at least O.S% but preferably no more than 30~ by weight, such as between 1.0~ and 15~ by weight of the composition.
~$~
The ratio by weight of the cationic fabric softening agent to the lanolin or lanolin-like material may lie between 0.05:l and 20:l, more preferably between O.l:l and lO.l, especially between l:l and 4:l.
In use, the fabric softening composition of the invention is added to a large volume of water to form a liquor with which the fabrics to be treated are contacted~
Generally, ~he total concentra~ion of the cationic fabric softening agent and the lanolin or lanolin-like materials in this liquor will be between about 50 ppm and about 500 ppm.
The pH o~ the aqueous composition used for forming the liquor may be varied within a range, for example between about 3 and about 8, preferably from about 4 to about 6. To achieve the desired pH in the composition and in the treatment liquor, the composition may contain buffering agents as required such as benzoic acid, ci~ric acid and phosphoric acids and~or their alkali metal salts.
In use, the fabrics to be treated are contacted with an aqueous liqucr to which the fabric softening composition is added, the ratio by weight of the fabrics to the liquor being preferably less than about 25:l, most preferably between about lO:l and about 4:l.
The aqueous liquor in contact with the fabrics may be at any convenient temperature. Successful. results can be 3 obtained when the liquor has a temperature between about O~C and about 60C, preferably between about 10C and about The liquor and fabrics in contact therewith are preferably agltated during treatment.
The amount of cationic softening agent and lanolin or lanolin~lîke material deposited on the fabric depends on, nter alia, the concentration of these components in the treatment liquor, the treatment temperature, the degree of agitation, the treatment time and the nature of the fabric. Generally, a level of less than about 0.5~, such as between about 0.0l% and about 0.4% by weight in total of these components ~ill be deposited, based on the weight of the dry fabric.
The balance of the composition comprises the aqueous medium, as the case may be with the other ingredients as set out below. The aqueous medium comprises at least 25%, preferably at least 30%, and especially at ~east 40% of the composition.
The compositions of the invention may further comprise additional beneficial ingredients, cornmonly used or proposed for inclusion in liquid fabric-softening compGsition~. Such ingredients, either a oi.c Ol-incorporated in suitable carriers, include additional viscosity modifiers, germicides, fluorescers, perfumes including deodorising perEumes, organic or inorganic acids, antistatic agents such as water-soluble cationic surfactants, ethoxylated quaternary polyamine compounds (eg Ethoduameen T i3~ and aluminium salts, soil-release agents, colourants, antioxidants, bleaches, bleach precursors, anti-yellowing agents, ironing aids etc, all in the conventional minor amounts. Enzymes such as cellulases 30 may also be included.
The compositions may also contain, in addition to the cationic abric-softening agents, other non-cationic fabric-softening agents such as nonionic fabric-softerling 35 agents.
In particular, the fabric softening compositions may include a ~iscosity modifier selected from polymers as described below, C12-C40 hydrocarbon5, Cg-C24 fatty acids, fatty acid esters having a total of 10 40 carbon atorns, C10-Cl8 fatty alcohols, water-miscible solvents, and elec-trolytes The polymer when included in the composition of the invention may be present therein in an amount of from 0.5 tc 40%, preferably from l to 30%, and particularly preferably 4-25~. The polymer, suitable for inclusion, is defined in the foLlowing way:
The polymer shGuld be water-soluble under user's conditions, and a 20% aqueous solution of the polymer should have a viscosity (~ ~ of ~50, preferably ~30 and especially preferably < 15 cP, as measured at 25C and 110 sec in a ElaaXe Viscometer. Said 20% aqueous solution should also show a vapour pressure equal to or lower than the vapour pressure of a 2~ aqueous solution of poly-ethyleneglycol with a molecular weight of 6,000, preferably equal to or lower than that of a 10~ aqueous solution of said polyethyleneglycol, and particulary preferably equal to or lower than that of an 18~ aqueous solution of said polyethyleneglycol. The said aqueous polymer solution can be of water and polymer only, or can include solvent-containing media normally derived from the raw materials or additives, or include additives specifically designed to improve the vapour pressure lowering capacity of the polymer, or, in the case of ionic polymers, include adjustments to pH in order to optimise ionisation. Such vapour pressure measurements can be obtained using an Hewlett Packard vapour pressure osmometer, using an operating temperature of 34.5C or using any other sultable vapour measuring device.
- g - C.1325 The polymer should furthermore have a molecular weight of at least 400, preferably at least 4,000 and particularly preferably at least 6,000.
It is desirable, furthermore, that the polymer does not negatively interact with any of the other ingredients of the composition.
Suitable examples of the polymer can be thus obtained 10 from the polyalkyleneglycols, the polyalkylene imines, de~tran, gelatin and other natural or synthetic (co)polymers, as lon~ as they meet the above criteria.
Mix~ures of two or more polymers of the same type or 15 of diffexent type may also be used.
A preferred class of polymers comprises polyethylene-glycols ~ith an average molecular weight of about l,000 to about 6,000. These polymers, and especially those 20 with an average molecular weight of 4,000 or 6,000, are particularly suitable for compositions of the invention with a high level of relatively water~insoluble cationic fabric-softening agent.
Other typical examples of suitable polymers are dextran with a molecular weight of lO,000 and polyethylene imine with a molecular weight of 45-750.
When the composition contains a C12-C~O hydro-30 carbon as a viscosity control agent, this is advantageously at a level of from 0.25% to 50~ by weight, preferably from 0.5% to 25%. Preferred materials have from 12 to 24 carbon a~oms and especially preferred are liquid mixtures of paraffins having from 14 to 18 carbon atoms.
Norn~ , suitable hydrocarbons are found in the paraffin ~s~ fin series, but other materials, such as alkynes and cyclic hydrocarbons are not excluded.
Materials known generally as paraffin oil, and petroleum 5 are suitable. Examples of specific materials are hexadecane, octadecane, eicosane tetradecane and octadecane. Preferred co~nercially-available paraffin mixtures include spindle oil and light oil and technical grade mixtures of Cl4 Cl8 n-paraffins Haloparaffins 10 such as myristyl chloride and stearyl bromide are not excluded.
When the composition contains a Cg-C~4 fatty acid, this i8 advantageously at a level of from 0.5 to 15%.
Highly preferred materials of this class are the Clo-C20 saturated fatty acids, especially lauric acid, myristic acid, palmitic acid and stearic acid.
When the composition contains a fatty acid ester having a total of lO to 40 carbon atoms this is at a preferred level of from 0.25 to 15% by weight, advantageously 0.5 to 4%. The ester is preferably empirically derived fro~ a atty acid having 8 to 23 carbon 25 atoms and an alkanol or hydroxy alkanol having 1-8, especially 1-4 carbon atoms. Specific examples include esters derived from Cl-C3 alcohols and lauric, myristic, palmitic or stearic acid, such as methyl laurate, ethyl myristate, iso-propyl stearate, ethylene glycol 30 monostearate, ethyl stearate, methyl palmitate, and other esters such as iso-butyl stearate and 2-ethylhexyllaurate, iso-octyl myristate.
When the composition contains a fatty alcohol having 35 from lO to l8 carbon atoms, this is preferably at a level of from 0.25 to 15~ by weight.
Specific examples of this class are decanol, dodecanol, tetradecanG1, pentadecanol, hexadecanol and octadecanol. The most preferred materials are lauryl and palmityl alcohols.
When the composition contains as viscosity control agent a solvent this may be a lower alkanol, a glycol, a glycolether and the like. The solvent may be present at a level of up to 20% by weight, such as from 5% to 10 15% by weight. ~hen the cationic fabric-softening agent is supplied in the form ~f an aqueous-alcoholic solution, that alcohol content is included in the above amounts ! and if necessary only a small amount of extra alcohol is to be added. A suitable solvent is 15 isopropanol.
The visc05ity oE the fabric softening composition may be controlled by the presence of an electrolyte.
Preferably the electrolyte is a water-soluble non~surface 20 active salt such as sodium chloride, sodiu."."~.i.osulphate, sodium benzoate, calcium chloride, magnesium chloride or aluminium chlorhydrate. The level of electrolyte will determine or be determined by the desired viscosity of the composition and the nature and concentration oE other 25 components in the composition. Typical level~ are from about 100 to about 1000 parts per million, most preferably between about 200 and about 500 parts per million.
The fabric ~oftening compo~itions optionally contain 30 one or more nonionic emulsifying agents, such as the polymerised monoglycerides of long chain f~ ids having from 14 to 24 carbon atoms in the straight or branched saturated or unsaturated carbon chain, suc~ ~5 ~oly-monolauryl glyceride, poly-monostearyl glyceride, poly-~5 monopalm.ityl glyceride or poly-monooleyl glyceride.
Another suitable nonîonic ernulsifying agent is sorbitan monostearate.
These nonionic emulsifying agents are available 5 commercially by the Trade Marks WITCONOL (Witco Chemicals Ltd) and SPAN (Atlas Chemical). The nonionic emulsifying agent may be present at a level from 0.5~ to 9.5% by weight, such as from 2.4% to 6%.
In addition to the above-discussed components, compositions according to the invention can also include a water-soluble cationic or non-ionic surfactant.
By water-soluble, it is meant that the surfactant has 15a solubility in water of pH 2.5 and 20~C of greater than 10 g/l. Normally such materials are alkyl subs~ituted ammonium salts having one C12-C2~ alkyl chain, optionally substituted or interrupted by functional groups such as -O , -COO -, -CONH -, -O - etc. Suitable ~water~soluble nonionic surfactants are the ethoxylates, sorbitan esters available as TWEENS (Atlas Chemical).
It is particularly beneficial to include a water-soluble cationic or nonionic emulsifying agent in the 25composition if it contains as a viscosity modifier a hydrocarbon, fatty acid, fatty alcohol or fatty acid ester of the types referred to above. The level of the water-soluble s~lrfactant is preferably 0.01% to l~o Preferably, the compositions contain substantially no anionic ma-terial 9uch as anionic surfactants. However some anionic material may be tolerated in practice. In preferred compositions the weight ratio of anu anionic material to the cationic fabric so~tening agent is less 35than 0.4:1, most preferably less than 0.2:1.
~t~
The viscosity of the fabric softening compositions i5 preferably less than about 150 cP, most preferably les~
than about 120 cP. This viscosity is measured at 25C and llO sec in a Haake Viscometer.
The compositions of the invention can normally be prepared by mixing the ingredients together in water, heating to a temperature of about 60C and agitating for 5-30 minutes.
The invention will now be illustrated by the following non-limiting examples.
Fabric conditioning compositions were made up according to the formulations given in the following Tables I and II by mixing the ingredients together in water at about 60C and agitating.
The cationic fabric softening a9~11L~ u~d were:
CFS 1 - Arosurf TA 100 (approx 700~ active) CFS 2 - Arquad 2HT (82.35% active) CFS 3 - VarisoEt 475~75~ active) CFS 4 - Di(soft tallow3 imidazoline methosulphate The lanolin used in each case was pure lanolin BP
(ex BDM).
r) ~ S ~ ~1 r /~s The viscosity modifying agents used were:
VMA 1 - n Cl~-C17 paraffin (ex BP~
V~A 2 - .sodium chloride VMA 3 - polyethylene glycol (MW 1.5K) VMA 4 - polyethylene glycol (MW 4K) VMA 5 - isopropanol VMA 6 - propylene glycol The water-soluble emulsifying agent used was Arquad 18 (50% active).
Each Table also gives the viscosity of the composition as measure in a Haake viscometer at 110 sec 15 and at 25C.
TABLE I
20 I~GREDIENTS (%) ....
CF5 1 2.0 4.0 2.5 CFS2 7~3 7~312.7 Lanolin 8.0 6.0 4.0 9.5905 9.5 25 Arquad l8 VMA 1 1 3 . 0 VM~ ~ 0 045 Water ~ -balance to lO0----~
Viscosity cP 24 29 187118 63 68 3~
TABI.E I I
EXP.MPLE NO 7 8 9 10 11 12 13 INGREDIENTS ( ~6 ) CFS 3 8.0 8.015.56.7 CFS 4 35.0 18.75 18.75 \ Lanolin ~ 4.0 9.09.59.0 5.0 6.25 6.25 Arquad 18 0.5 10 VMA 1 1~.0 VMA ~ 0.015 0.1 0.32 0.25 ~MA 3 12.0 VMA ~ 10.0 12.0 ~MA 5 8.4 4.5 4.5 15 VMA 6 1.0 1.0 Perfume 1.5 Water ~ balance to 100-~
Viscosity cP 92 115125 183 180 71 151 Similar results can be achieved when Arquad 2T ~ex Armak) is used as the cationic fabric softener. Similar results can also b~ achieved when lanolin BP is replaced with Coronet grade lanolin ~e~ Croda) or Lanolin P95 (ex Westbrook Lanolin Co). Still further similar results can 25 be achieved by using calcium chloride, magnesium chloride or aluminium chlorhydrate.
Fabric conditioning compositions were made up according to the formulations given in the following Table III by mixing the ingredients together in water at about 60C and agitatlng. Product ~iscositie~ were measured as in Examples 1 to 13.
'~/C~ 5 ,~ /e /~
TABLE III
EXA ~LE N0: 14 15 INGREDIENTS %
-Arosurf TA 100 ~100~ active) 10.5 Varisoft 475 (75~ active) I.505 L,anolin 9 5 9 5 Aluminium chlorhydrate (as a 50~ solution) 1.0~ 0.3 10 Water balance to 100 Viscosity cP 196 ~2 *Percentage o solid.
~he following dilute fabric softening compositions were prepared:
20 EXAMPLE N0:
INGREDIENTS (%) 16 17 18 _ Arquad 2HT 4.0 8.0 8.0 Coronet grade lanolin (ex Croda) 1.0 25 Lanolin P95 (ex Westbrook) - 1.0 1.0 Calcium chloride - 0.1 0.1 Water, perfume, dye --balance to 100~-Viscosity (110 sec ~ 3 23 24 ¢~
~1-EXA ~LES l9 AND 20 The following fabric softening compositions were prepared using lanolin-like materials in place of lanolin per se:
EXAMPLE N0: l9 ~0 INGREDIENTS (~) -10 Arquad 2HT 8.0 l2.25 Super Hartolan 3.0 Iso-stearic acid 2.75 Calcium chloride O.l 0.2 Water --balance to lO0~-~5 Viscosity at llO sec '(Cp) 13 126 Notes: l - Distilled lanolin alcohols (ex Croda Chemicals)
_ FIELD OF THE INVE~ION
,.. . .
The present invention relates to a fabric softening composition. In particular, but not exclusively, it 5 relates to an aqueous based concentrated fabric softening composition.
BACKGROUND ART
It is known to treat fabrics, particularly after washing, with fabric softening agents in order to improve the feel of the fabrics and, in the case of clothes, to improve the comfort in wear. Traditionally, fabric softening agents are applied from an aqueous liquor which 15 is made up by adding a relatively small volume of a fabric soEtening composition to a large volume of water, for example during the rinse cycle in an automatic washing machine. The fabric softening composition is usually an aqueous liquid product containing less than ahout 8~ of a 20 cationic fabric softening agent. For a number of reasons, including or example the cost of packaging, it would be preferred if the product were to contain more than 8% of the active ingredient but due to difficulties in 3~
manufacture, storage and ease of use of the products, it has only been possible to do this in the past with some difficulty.
Further, there may be a desire to partially replace the cationic fabric softening agent with a material which is less costly, easier to handle or less prone to causing skin reaction w~-ile at the same time maintaining or substantially maintaining the performance of the productO
As set out in more detail below, the present invention seeks to overcome one or more of the objectives referred to above by the combined use of a cationic fabric softening agent and lanolin or a lanolin-like material.
SUMM~RY OF TH~ INVENTION
According to the invention there is provided a fabric softening composition comprising an aqueous base and at least 0.5~ by weight of a cationic fabric softening agent, characterised in that it further comprises from 0.25% up to 10% by weight of lanolin or a lanolin-like material.
An essential component of the present invention is lanolin or a lanolin-like material. Lanolin is wool wax which has been purified by various purification steps including washing, neutralisation, filtration, bleaching and deodorisation. Lanolin is composed primarily of esters which constitute the active constituents in the present invention and which yield on hydrolysis a mixture of complex alcohols and fatty acids. The alcohols which form about half of the ester component by weight, include sterols and terpene alcohols. The sterols amount to about 30% and include cholesterol, 7-dehydrocholesterol and cerebosterol and dihydrocholesterol (cholestanol). The terpene alcohols include lanesterol (C30H50O), dih~drlaneSterl (C30H52)' agnosterol (C30H48o)~
dihydroagnosterol (C30H500).
Lanolin is available commercially in a number of forms. Lanolin as such contains the active constituents primarily in their ester form. It is also available in two hydrolysed forms where the active constituents are primarily in their alcoholic or carboxylic acid form.
Further, lanolin may be hydrogenated to form a product where the active constituents are present primarily only in their alcoholic form. Lanolin is also commercially available in propo~ylated and acetylated forms. As used herein the term "lanolin" is intended to refer to any such material derived from wool wax whether the active constituents are in the alco~olic, ester, alkoxylated, hydrogenated or other chemical form.
Suitable commercial forms of lanolin include Corona (lanolin BP~, ~artolan, Polychol and Coronet (Trade Marks of Croda Chemicals Ltd), Solulan, Acetulan and Modulan (Trade Marks of American Cholesterol Products Inc) and Lanocerina ~Trade Mark - Esperis SpA Milan). Commercial lanolin is also available from Westbrook Lanolin Co., Bradford, England.
Many of the active constituents of lanolin can be prepared synthetically, from sources other than wool WAX
or can be ~xtracted from wool wax and other naturally occurring material~. While for cost reasons the commercially available forms of lanolin are preferred for the present invention, it is also possible to use any one or more of the active constituents referred to above however derived, and also materials of similar structure.
Thu , in place of lanolin one may use a "lanolin-like material" which term as used herein includes ~2~
ta) any Ol~ or more of the active lanolin constituents ref~ .o above, and the carboxylic acid or alcohol, derivatives thereof;
5 (b) the corresponding carboxylic acids or alcohols and ester derivatives of the material~ listed in (a), in particular the esters thereof with fatty acids or alcohols containing at least 12 carbon atoms.
10 ~c) iso- and anteiso- alcohols and acids and derivatives thereof having the general formula CH- Rl -X
where Rl is a divalent straight or branched chain, saturated or unsaturated, substituted or unsubstituted hydrocarbyl group having at least 7, preferably at least 15 carbon atoms, R2 is a methyl or ethyl group and X is OH, -COOH, -O -C -R or ~COOR ~here R is a hydrocarhyl group, in particular a fatty acid alkyl group containing of at least 12 carbon atoms. Examples of materials in this group include 16-methyl heptadecanol, 24-methyl hexacosanol, 8-methyl nonanoic acid: and 2-hydroxy-16-methyl heptadecanoic acid.
The level of lanolin or lanolin-like material in the fabric softening compositions is from 0.25% up to 10% by weight, such as between 0.5% and 5% by weight of the 35 composition.
3~ a3 Any well-known cationic fabric softening agent can be used in the present invention, as well as mixtures of two or more of such agents.
Suitable e~amples of cat.ionic fabric-softening agents are quaternary ammonium compounds containing two long alkyl or alkenyl chains with 12-22 carbon atoms such as di(hardened or unhardened tallow) dimethyl ammonium-chloride~ 2-heptadecyl-2methylstearoyl amido ethyl imida~oline methosulphate, di-(coco)dimethyl ammoni.um-chloride, etc. These cationic fabric-softening agents are well-known in the art and furthex suitable examples can be found in Schwartz-Perry. "Surface-actiYe Agents and Detergents" Yol II, 1958.
~5 Relatively water-soluble cationic softening agents, such as the monoalkyl quaternary ammonium compounds s~ch as stearyltrimethylammoniumchloride, may also be used, but, as they are often less effective softeners, they are preferably used in conjunction with other, more effective cationic fabric softening agents or witi, llu,~ Lionic softening agents such as fatty acid esters of polyols such as sorbitantristearate, glycerolmonostearate, and so on, or with anîonic detergents with which they are capable of forming softening compl.exes, such as fatty acid soaps.
They may also be made more hydrophobic by treatment with suitable hydrophobising agents such as long chain alcohols and fatty acids. The present invention is however of particular benefit if the more effective, less water-soluble cationic softening agents having two long alkylchains are used.
The level of cationic fabric softening agent in the aqueous fabric softening compositions is at least O.S% but preferably no more than 30~ by weight, such as between 1.0~ and 15~ by weight of the composition.
~$~
The ratio by weight of the cationic fabric softening agent to the lanolin or lanolin-like material may lie between 0.05:l and 20:l, more preferably between O.l:l and lO.l, especially between l:l and 4:l.
In use, the fabric softening composition of the invention is added to a large volume of water to form a liquor with which the fabrics to be treated are contacted~
Generally, ~he total concentra~ion of the cationic fabric softening agent and the lanolin or lanolin-like materials in this liquor will be between about 50 ppm and about 500 ppm.
The pH o~ the aqueous composition used for forming the liquor may be varied within a range, for example between about 3 and about 8, preferably from about 4 to about 6. To achieve the desired pH in the composition and in the treatment liquor, the composition may contain buffering agents as required such as benzoic acid, ci~ric acid and phosphoric acids and~or their alkali metal salts.
In use, the fabrics to be treated are contacted with an aqueous liqucr to which the fabric softening composition is added, the ratio by weight of the fabrics to the liquor being preferably less than about 25:l, most preferably between about lO:l and about 4:l.
The aqueous liquor in contact with the fabrics may be at any convenient temperature. Successful. results can be 3 obtained when the liquor has a temperature between about O~C and about 60C, preferably between about 10C and about The liquor and fabrics in contact therewith are preferably agltated during treatment.
The amount of cationic softening agent and lanolin or lanolin~lîke material deposited on the fabric depends on, nter alia, the concentration of these components in the treatment liquor, the treatment temperature, the degree of agitation, the treatment time and the nature of the fabric. Generally, a level of less than about 0.5~, such as between about 0.0l% and about 0.4% by weight in total of these components ~ill be deposited, based on the weight of the dry fabric.
The balance of the composition comprises the aqueous medium, as the case may be with the other ingredients as set out below. The aqueous medium comprises at least 25%, preferably at least 30%, and especially at ~east 40% of the composition.
The compositions of the invention may further comprise additional beneficial ingredients, cornmonly used or proposed for inclusion in liquid fabric-softening compGsition~. Such ingredients, either a oi.c Ol-incorporated in suitable carriers, include additional viscosity modifiers, germicides, fluorescers, perfumes including deodorising perEumes, organic or inorganic acids, antistatic agents such as water-soluble cationic surfactants, ethoxylated quaternary polyamine compounds (eg Ethoduameen T i3~ and aluminium salts, soil-release agents, colourants, antioxidants, bleaches, bleach precursors, anti-yellowing agents, ironing aids etc, all in the conventional minor amounts. Enzymes such as cellulases 30 may also be included.
The compositions may also contain, in addition to the cationic abric-softening agents, other non-cationic fabric-softening agents such as nonionic fabric-softerling 35 agents.
In particular, the fabric softening compositions may include a ~iscosity modifier selected from polymers as described below, C12-C40 hydrocarbon5, Cg-C24 fatty acids, fatty acid esters having a total of 10 40 carbon atorns, C10-Cl8 fatty alcohols, water-miscible solvents, and elec-trolytes The polymer when included in the composition of the invention may be present therein in an amount of from 0.5 tc 40%, preferably from l to 30%, and particularly preferably 4-25~. The polymer, suitable for inclusion, is defined in the foLlowing way:
The polymer shGuld be water-soluble under user's conditions, and a 20% aqueous solution of the polymer should have a viscosity (~ ~ of ~50, preferably ~30 and especially preferably < 15 cP, as measured at 25C and 110 sec in a ElaaXe Viscometer. Said 20% aqueous solution should also show a vapour pressure equal to or lower than the vapour pressure of a 2~ aqueous solution of poly-ethyleneglycol with a molecular weight of 6,000, preferably equal to or lower than that of a 10~ aqueous solution of said polyethyleneglycol, and particulary preferably equal to or lower than that of an 18~ aqueous solution of said polyethyleneglycol. The said aqueous polymer solution can be of water and polymer only, or can include solvent-containing media normally derived from the raw materials or additives, or include additives specifically designed to improve the vapour pressure lowering capacity of the polymer, or, in the case of ionic polymers, include adjustments to pH in order to optimise ionisation. Such vapour pressure measurements can be obtained using an Hewlett Packard vapour pressure osmometer, using an operating temperature of 34.5C or using any other sultable vapour measuring device.
- g - C.1325 The polymer should furthermore have a molecular weight of at least 400, preferably at least 4,000 and particularly preferably at least 6,000.
It is desirable, furthermore, that the polymer does not negatively interact with any of the other ingredients of the composition.
Suitable examples of the polymer can be thus obtained 10 from the polyalkyleneglycols, the polyalkylene imines, de~tran, gelatin and other natural or synthetic (co)polymers, as lon~ as they meet the above criteria.
Mix~ures of two or more polymers of the same type or 15 of diffexent type may also be used.
A preferred class of polymers comprises polyethylene-glycols ~ith an average molecular weight of about l,000 to about 6,000. These polymers, and especially those 20 with an average molecular weight of 4,000 or 6,000, are particularly suitable for compositions of the invention with a high level of relatively water~insoluble cationic fabric-softening agent.
Other typical examples of suitable polymers are dextran with a molecular weight of lO,000 and polyethylene imine with a molecular weight of 45-750.
When the composition contains a C12-C~O hydro-30 carbon as a viscosity control agent, this is advantageously at a level of from 0.25% to 50~ by weight, preferably from 0.5% to 25%. Preferred materials have from 12 to 24 carbon a~oms and especially preferred are liquid mixtures of paraffins having from 14 to 18 carbon atoms.
Norn~ , suitable hydrocarbons are found in the paraffin ~s~ fin series, but other materials, such as alkynes and cyclic hydrocarbons are not excluded.
Materials known generally as paraffin oil, and petroleum 5 are suitable. Examples of specific materials are hexadecane, octadecane, eicosane tetradecane and octadecane. Preferred co~nercially-available paraffin mixtures include spindle oil and light oil and technical grade mixtures of Cl4 Cl8 n-paraffins Haloparaffins 10 such as myristyl chloride and stearyl bromide are not excluded.
When the composition contains a Cg-C~4 fatty acid, this i8 advantageously at a level of from 0.5 to 15%.
Highly preferred materials of this class are the Clo-C20 saturated fatty acids, especially lauric acid, myristic acid, palmitic acid and stearic acid.
When the composition contains a fatty acid ester having a total of lO to 40 carbon atoms this is at a preferred level of from 0.25 to 15% by weight, advantageously 0.5 to 4%. The ester is preferably empirically derived fro~ a atty acid having 8 to 23 carbon 25 atoms and an alkanol or hydroxy alkanol having 1-8, especially 1-4 carbon atoms. Specific examples include esters derived from Cl-C3 alcohols and lauric, myristic, palmitic or stearic acid, such as methyl laurate, ethyl myristate, iso-propyl stearate, ethylene glycol 30 monostearate, ethyl stearate, methyl palmitate, and other esters such as iso-butyl stearate and 2-ethylhexyllaurate, iso-octyl myristate.
When the composition contains a fatty alcohol having 35 from lO to l8 carbon atoms, this is preferably at a level of from 0.25 to 15~ by weight.
Specific examples of this class are decanol, dodecanol, tetradecanG1, pentadecanol, hexadecanol and octadecanol. The most preferred materials are lauryl and palmityl alcohols.
When the composition contains as viscosity control agent a solvent this may be a lower alkanol, a glycol, a glycolether and the like. The solvent may be present at a level of up to 20% by weight, such as from 5% to 10 15% by weight. ~hen the cationic fabric-softening agent is supplied in the form ~f an aqueous-alcoholic solution, that alcohol content is included in the above amounts ! and if necessary only a small amount of extra alcohol is to be added. A suitable solvent is 15 isopropanol.
The visc05ity oE the fabric softening composition may be controlled by the presence of an electrolyte.
Preferably the electrolyte is a water-soluble non~surface 20 active salt such as sodium chloride, sodiu."."~.i.osulphate, sodium benzoate, calcium chloride, magnesium chloride or aluminium chlorhydrate. The level of electrolyte will determine or be determined by the desired viscosity of the composition and the nature and concentration oE other 25 components in the composition. Typical level~ are from about 100 to about 1000 parts per million, most preferably between about 200 and about 500 parts per million.
The fabric ~oftening compo~itions optionally contain 30 one or more nonionic emulsifying agents, such as the polymerised monoglycerides of long chain f~ ids having from 14 to 24 carbon atoms in the straight or branched saturated or unsaturated carbon chain, suc~ ~5 ~oly-monolauryl glyceride, poly-monostearyl glyceride, poly-~5 monopalm.ityl glyceride or poly-monooleyl glyceride.
Another suitable nonîonic ernulsifying agent is sorbitan monostearate.
These nonionic emulsifying agents are available 5 commercially by the Trade Marks WITCONOL (Witco Chemicals Ltd) and SPAN (Atlas Chemical). The nonionic emulsifying agent may be present at a level from 0.5~ to 9.5% by weight, such as from 2.4% to 6%.
In addition to the above-discussed components, compositions according to the invention can also include a water-soluble cationic or non-ionic surfactant.
By water-soluble, it is meant that the surfactant has 15a solubility in water of pH 2.5 and 20~C of greater than 10 g/l. Normally such materials are alkyl subs~ituted ammonium salts having one C12-C2~ alkyl chain, optionally substituted or interrupted by functional groups such as -O , -COO -, -CONH -, -O - etc. Suitable ~water~soluble nonionic surfactants are the ethoxylates, sorbitan esters available as TWEENS (Atlas Chemical).
It is particularly beneficial to include a water-soluble cationic or nonionic emulsifying agent in the 25composition if it contains as a viscosity modifier a hydrocarbon, fatty acid, fatty alcohol or fatty acid ester of the types referred to above. The level of the water-soluble s~lrfactant is preferably 0.01% to l~o Preferably, the compositions contain substantially no anionic ma-terial 9uch as anionic surfactants. However some anionic material may be tolerated in practice. In preferred compositions the weight ratio of anu anionic material to the cationic fabric so~tening agent is less 35than 0.4:1, most preferably less than 0.2:1.
~t~
The viscosity of the fabric softening compositions i5 preferably less than about 150 cP, most preferably les~
than about 120 cP. This viscosity is measured at 25C and llO sec in a Haake Viscometer.
The compositions of the invention can normally be prepared by mixing the ingredients together in water, heating to a temperature of about 60C and agitating for 5-30 minutes.
The invention will now be illustrated by the following non-limiting examples.
Fabric conditioning compositions were made up according to the formulations given in the following Tables I and II by mixing the ingredients together in water at about 60C and agitating.
The cationic fabric softening a9~11L~ u~d were:
CFS 1 - Arosurf TA 100 (approx 700~ active) CFS 2 - Arquad 2HT (82.35% active) CFS 3 - VarisoEt 475~75~ active) CFS 4 - Di(soft tallow3 imidazoline methosulphate The lanolin used in each case was pure lanolin BP
(ex BDM).
r) ~ S ~ ~1 r /~s The viscosity modifying agents used were:
VMA 1 - n Cl~-C17 paraffin (ex BP~
V~A 2 - .sodium chloride VMA 3 - polyethylene glycol (MW 1.5K) VMA 4 - polyethylene glycol (MW 4K) VMA 5 - isopropanol VMA 6 - propylene glycol The water-soluble emulsifying agent used was Arquad 18 (50% active).
Each Table also gives the viscosity of the composition as measure in a Haake viscometer at 110 sec 15 and at 25C.
TABLE I
20 I~GREDIENTS (%) ....
CF5 1 2.0 4.0 2.5 CFS2 7~3 7~312.7 Lanolin 8.0 6.0 4.0 9.5905 9.5 25 Arquad l8 VMA 1 1 3 . 0 VM~ ~ 0 045 Water ~ -balance to lO0----~
Viscosity cP 24 29 187118 63 68 3~
TABI.E I I
EXP.MPLE NO 7 8 9 10 11 12 13 INGREDIENTS ( ~6 ) CFS 3 8.0 8.015.56.7 CFS 4 35.0 18.75 18.75 \ Lanolin ~ 4.0 9.09.59.0 5.0 6.25 6.25 Arquad 18 0.5 10 VMA 1 1~.0 VMA ~ 0.015 0.1 0.32 0.25 ~MA 3 12.0 VMA ~ 10.0 12.0 ~MA 5 8.4 4.5 4.5 15 VMA 6 1.0 1.0 Perfume 1.5 Water ~ balance to 100-~
Viscosity cP 92 115125 183 180 71 151 Similar results can be achieved when Arquad 2T ~ex Armak) is used as the cationic fabric softener. Similar results can also b~ achieved when lanolin BP is replaced with Coronet grade lanolin ~e~ Croda) or Lanolin P95 (ex Westbrook Lanolin Co). Still further similar results can 25 be achieved by using calcium chloride, magnesium chloride or aluminium chlorhydrate.
Fabric conditioning compositions were made up according to the formulations given in the following Table III by mixing the ingredients together in water at about 60C and agitatlng. Product ~iscositie~ were measured as in Examples 1 to 13.
'~/C~ 5 ,~ /e /~
TABLE III
EXA ~LE N0: 14 15 INGREDIENTS %
-Arosurf TA 100 ~100~ active) 10.5 Varisoft 475 (75~ active) I.505 L,anolin 9 5 9 5 Aluminium chlorhydrate (as a 50~ solution) 1.0~ 0.3 10 Water balance to 100 Viscosity cP 196 ~2 *Percentage o solid.
~he following dilute fabric softening compositions were prepared:
20 EXAMPLE N0:
INGREDIENTS (%) 16 17 18 _ Arquad 2HT 4.0 8.0 8.0 Coronet grade lanolin (ex Croda) 1.0 25 Lanolin P95 (ex Westbrook) - 1.0 1.0 Calcium chloride - 0.1 0.1 Water, perfume, dye --balance to 100~-Viscosity (110 sec ~ 3 23 24 ¢~
~1-EXA ~LES l9 AND 20 The following fabric softening compositions were prepared using lanolin-like materials in place of lanolin per se:
EXAMPLE N0: l9 ~0 INGREDIENTS (~) -10 Arquad 2HT 8.0 l2.25 Super Hartolan 3.0 Iso-stearic acid 2.75 Calcium chloride O.l 0.2 Water --balance to lO0~-~5 Viscosity at llO sec '(Cp) 13 126 Notes: l - Distilled lanolin alcohols (ex Croda Chemicals)
2 - Iso-stearic acid (e~ Emery) E~AMPLE 2l _ Two fabric softening compositions were prepared according to the following7 Table.
EXAMPLE: A B
NGREDENT (%) 3o Arquad 2HT 8.G 8.0 Coronet lanolin l.0 ~.^
Water balance to lO0 35 Cationic/lanolin ratio 8 l 2A
~$.~
Pieces of cotton terry cloth were treated with liquors made up from these compositlons. The treated cloths were assessed by a panel of people who found that composition B gave more preferred results than composition A.
Except as indicated otherwise, all percentages referred to herein are by weight, based on the weight of the composition.
EXAMPLE: A B
NGREDENT (%) 3o Arquad 2HT 8.G 8.0 Coronet lanolin l.0 ~.^
Water balance to lO0 35 Cationic/lanolin ratio 8 l 2A
~$.~
Pieces of cotton terry cloth were treated with liquors made up from these compositlons. The treated cloths were assessed by a panel of people who found that composition B gave more preferred results than composition A.
Except as indicated otherwise, all percentages referred to herein are by weight, based on the weight of the composition.
Claims (5)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A fabric softening composition comprising an aqueous base and at least 0.5% by weight of a cationic fabric softening agent, characterised in that it further comprises from 0.25% to 10% by weight of lanolin or a lanolin-like material.
2. A fabric softening composition according to claim 1, characterised in that the weight ratio of said lanolin or lanolin-like material to said cationic fabric softening agent lies between 0.05:1 and 20:1.
3. A fabric softening composition according to claim 1, characterised in that the weight ratio of said lanolin or lanolin-like material to said cationic fabric softening agent lies between 0.1:1 and 10:1.
4. A fabric softening composition according to claim 1, characterised in that it contains from 0.5% to 30% by weight of said cationic fabric softening agent and from 0.5% to 5% by weight of said lanolin or lanolin-like material.
5. A fabric softening composition according to claim 4, characterised in that it contains from 1.0% to 15% by weight of said fabric softening agent.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8203881 | 1982-02-10 | ||
| GB8203881 | 1982-02-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1192003A true CA1192003A (en) | 1985-08-20 |
Family
ID=10528228
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000420859A Expired CA1192003A (en) | 1982-02-10 | 1983-02-03 | Fabric softening composition |
Country Status (14)
| Country | Link |
|---|---|
| EP (1) | EP0088520B1 (en) |
| JP (1) | JPS58149380A (en) |
| AT (1) | ATE42570T1 (en) |
| BR (1) | BR8300643A (en) |
| CA (1) | CA1192003A (en) |
| DE (1) | DE3379733D1 (en) |
| GB (1) | GB2114618B (en) |
| GR (1) | GR77963B (en) |
| IN (1) | IN156622B (en) |
| NO (1) | NO830421L (en) |
| PH (1) | PH17958A (en) |
| PT (1) | PT76218B (en) |
| ZA (1) | ZA83878B (en) |
| ZW (1) | ZW3583A1 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR8305694A (en) * | 1982-10-21 | 1984-07-10 | Unilever Nv | PROCESS FOR DRYING CONDITIONS IN THE RINSE STAGES AND LIQUID DRYING CONDITIONING COMPOSITION |
| GB8410318D0 (en) * | 1984-04-19 | 1984-05-31 | Unilever Plc | Fabric softening composition |
| CN101522877A (en) | 2006-10-06 | 2009-09-02 | 陶氏康宁公司 | Process for preparing fabric softener compositions |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1030308A (en) * | 1972-10-10 | 1978-05-02 | Neil M. Mchugh | Conditioning of fabrics |
| IT966940B (en) * | 1972-12-05 | 1974-02-20 | Unilever Nv | DETERGENT COMPOSITION |
| US4110498A (en) * | 1976-03-08 | 1978-08-29 | The Procter & Gamble Company | Fabric treatment compositions |
| GB2007734B (en) * | 1977-10-22 | 1983-04-07 | Cargo Fleet Chemical Co | Fabric softeners |
| DE2966013D1 (en) * | 1979-01-11 | 1983-09-01 | Procter & Gamble | Concentrated fabric softening composition |
-
1983
- 1983-02-03 PH PH28478A patent/PH17958A/en unknown
- 1983-02-03 CA CA000420859A patent/CA1192003A/en not_active Expired
- 1983-02-04 ZW ZW35/83A patent/ZW3583A1/en unknown
- 1983-02-07 IN IN37/BOM/83A patent/IN156622B/en unknown
- 1983-02-07 GR GR70434A patent/GR77963B/el unknown
- 1983-02-08 AT AT83300625T patent/ATE42570T1/en not_active IP Right Cessation
- 1983-02-08 DE DE8383300625T patent/DE3379733D1/en not_active Expired
- 1983-02-08 GB GB08303393A patent/GB2114618B/en not_active Expired
- 1983-02-08 EP EP83300625A patent/EP0088520B1/en not_active Expired
- 1983-02-09 JP JP58020538A patent/JPS58149380A/en active Pending
- 1983-02-09 BR BR8300643A patent/BR8300643A/en not_active IP Right Cessation
- 1983-02-09 NO NO830421A patent/NO830421L/en unknown
- 1983-02-09 PT PT76218A patent/PT76218B/en unknown
- 1983-02-09 ZA ZA83878A patent/ZA83878B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ZW3583A1 (en) | 1984-08-29 |
| GB8303393D0 (en) | 1983-03-16 |
| IN156622B (en) | 1985-09-21 |
| JPS58149380A (en) | 1983-09-05 |
| ATE42570T1 (en) | 1989-05-15 |
| BR8300643A (en) | 1983-11-08 |
| GB2114618A (en) | 1983-08-24 |
| DE3379733D1 (en) | 1989-06-01 |
| PT76218A (en) | 1983-03-01 |
| PT76218B (en) | 1986-07-14 |
| PH17958A (en) | 1985-02-20 |
| GR77963B (en) | 1984-09-25 |
| NO830421L (en) | 1983-08-11 |
| GB2114618B (en) | 1986-05-21 |
| ZA83878B (en) | 1984-09-26 |
| EP0088520B1 (en) | 1989-04-26 |
| EP0088520A2 (en) | 1983-09-14 |
| EP0088520A3 (en) | 1986-02-26 |
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