EP1412467B1 - Composition adoucissante pour tissu - Google Patents
Composition adoucissante pour tissu Download PDFInfo
- Publication number
- EP1412467B1 EP1412467B1 EP02745044A EP02745044A EP1412467B1 EP 1412467 B1 EP1412467 B1 EP 1412467B1 EP 02745044 A EP02745044 A EP 02745044A EP 02745044 A EP02745044 A EP 02745044A EP 1412467 B1 EP1412467 B1 EP 1412467B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- fragrance
- fabric softener
- fabric
- oil
- composition according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 64
- 239000002979 fabric softener Substances 0.000 title claims abstract description 42
- 239000003205 fragrance Substances 0.000 claims abstract description 58
- 239000012071 phase Substances 0.000 claims abstract description 33
- 239000002752 cationic softener Substances 0.000 claims abstract description 31
- 239000008346 aqueous phase Substances 0.000 claims abstract description 20
- 239000004744 fabric Substances 0.000 claims abstract description 19
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 13
- 239000006185 dispersion Substances 0.000 claims abstract description 8
- 239000003921 oil Substances 0.000 claims description 23
- -1 amido amines Chemical class 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims description 5
- 239000010696 ester oil Substances 0.000 claims description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- 238000013019 agitation Methods 0.000 claims description 4
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical class C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 claims description 4
- 229920002545 silicone oil Polymers 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims 1
- 235000019198 oils Nutrition 0.000 description 17
- 125000001183 hydrocarbyl group Chemical group 0.000 description 11
- 150000003839 salts Chemical class 0.000 description 10
- 150000001450 anions Chemical group 0.000 description 9
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 8
- 239000003760 tallow Substances 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 7
- 125000003342 alkenyl group Chemical group 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000005191 phase separation Methods 0.000 description 6
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- JOZKFWLRHCDGJA-UHFFFAOYSA-N citronellol acetate Chemical compound CC(=O)OCCC(C)CCC=C(C)C JOZKFWLRHCDGJA-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 150000004820 halides Chemical class 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000002736 nonionic surfactant Substances 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 229940074928 isopropyl myristate Drugs 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000000546 pharmaceutical excipient Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- DBHODFSFBXJZNY-UHFFFAOYSA-N 2,4-dichlorobenzyl alcohol Chemical compound OCC1=CC=C(Cl)C=C1Cl DBHODFSFBXJZNY-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 0 C*(C)(C(**)**)N** Chemical compound C*(C)(C(**)**)N** 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- JOZKFWLRHCDGJA-LLVKDONJSA-N Citronellyl acetate Natural products CC(=O)OCC[C@H](C)CCC=C(C)C JOZKFWLRHCDGJA-LLVKDONJSA-N 0.000 description 2
- 102100037316 F-box/LRR-repeat protein 4 Human genes 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 2
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 2
- 239000005792 Geraniol Substances 0.000 description 2
- 101001026867 Homo sapiens F-box/LRR-repeat protein 4 Proteins 0.000 description 2
- 101001026853 Homo sapiens F-box/LRR-repeat protein 5 Proteins 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- KGEKLUUHTZCSIP-HOSYDEDBSA-N [(1s,4s,6r)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] acetate Chemical compound C1C[C@]2(C)[C@H](OC(=O)C)C[C@H]1C2(C)C KGEKLUUHTZCSIP-HOSYDEDBSA-N 0.000 description 2
- 229940022663 acetate Drugs 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000011149 active material Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 2
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 2
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- XVBRCOKDZVQYAY-UHFFFAOYSA-N bronidox Chemical compound [O-][N+](=O)C1(Br)COCOC1 XVBRCOKDZVQYAY-UHFFFAOYSA-N 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229960004698 dichlorobenzyl alcohol Drugs 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 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
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- KIWBPDUYBMNFTB-UHFFFAOYSA-M ethyl sulfate Chemical compound CCOS([O-])(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-M 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 229940113087 geraniol Drugs 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 2
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 2
- LUKNLVTZDZMBOU-UHFFFAOYSA-N n-ethoxymethanamine Chemical compound CCONC LUKNLVTZDZMBOU-UHFFFAOYSA-N 0.000 description 2
- RRUADNNEIGVWSQ-UHFFFAOYSA-N n-ethyl-n-methylhydroxylamine Chemical compound CCN(C)O RRUADNNEIGVWSQ-UHFFFAOYSA-N 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- XHXUANMFYXWVNG-UHFFFAOYSA-N (+/-)-Menthyl acetate Chemical compound CC(C)C1CCC(C)CC1OC(C)=O XHXUANMFYXWVNG-UHFFFAOYSA-N 0.000 description 1
- BGCIAWBDYRWKEK-UHFFFAOYSA-N (1-butylcyclohexyl) acetate Chemical compound CCCCC1(OC(C)=O)CCCCC1 BGCIAWBDYRWKEK-UHFFFAOYSA-N 0.000 description 1
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 1
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 1
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 1
- ZGOQRUPIKZGTLQ-UHFFFAOYSA-N 1,2-benzothiazole 1-oxide;sodium Chemical compound [Na].C1=CC=C2S(=O)N=CC2=C1 ZGOQRUPIKZGTLQ-UHFFFAOYSA-N 0.000 description 1
- JLJNZJNPAYILPJ-XYJRJTJESA-M 1-[1-[(z)-octadec-9-enyl]-4,5-dihydroimidazol-1-ium-1-yl]tetradecan-1-ol;chloride Chemical compound [Cl-].CCCCCCCC\C=C/CCCCCCCC[N+]1(C(O)CCCCCCCCCCCCC)CCN=C1 JLJNZJNPAYILPJ-XYJRJTJESA-M 0.000 description 1
- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 1
- JBMMTNRBVCXMHJ-UHFFFAOYSA-N 2-[1-(2-phenylethoxy)ethoxy]ethylbenzene Chemical compound C=1C=CC=CC=1CCOC(C)OCCC1=CC=CC=C1 JBMMTNRBVCXMHJ-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
- 229940046305 5-bromo-5-nitro-1,3-dioxane Drugs 0.000 description 1
- AMEMLELAMQEAIA-UHFFFAOYSA-N 6-(tert-butyl)thieno[3,2-d]pyrimidin-4(3H)-one Chemical compound N1C=NC(=O)C2=C1C=C(C(C)(C)C)S2 AMEMLELAMQEAIA-UHFFFAOYSA-N 0.000 description 1
- IHLDEDLAZNFOJB-UHFFFAOYSA-N 6-octoxy-6-oxohexanoic acid Chemical compound CCCCCCCCOC(=O)CCCCC(O)=O IHLDEDLAZNFOJB-UHFFFAOYSA-N 0.000 description 1
- VUFZVGQUAVDKMC-UHFFFAOYSA-N Allyl phenoxyacetate Chemical compound C=CCOC(=O)COC1=CC=CC=C1 VUFZVGQUAVDKMC-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 1
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241000234269 Liliales Species 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- BAECOWNUKCLBPZ-HIUWNOOHSA-N Triolein Natural products O([C@H](OCC(=O)CCCCCCC/C=C\CCCCCCCC)COC(=O)CCCCCCC/C=C\CCCCCCCC)C(=O)CCCCCCC/C=C\CCCCCCCC BAECOWNUKCLBPZ-HIUWNOOHSA-N 0.000 description 1
- PHYFQTYBJUILEZ-UHFFFAOYSA-N Trioleoylglycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCCCCCCCC)COC(=O)CCCCCCCC=CCCCCCCCC PHYFQTYBJUILEZ-UHFFFAOYSA-N 0.000 description 1
- GORMSINSWZJIKL-UHFFFAOYSA-N [3-(2-ethylhexanoyloxy)-2,2-dimethylpropyl] 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)OCC(C)(C)COC(=O)C(CC)CCCC GORMSINSWZJIKL-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 235000001053 badasse Nutrition 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229940007550 benzyl acetate Drugs 0.000 description 1
- 229960002903 benzyl benzoate Drugs 0.000 description 1
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 229940115397 bornyl acetate Drugs 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- UXVMQQNJUSDDNG-HDMMMHCHSA-L calcium-45(2+);dichloride Chemical compound [Cl-].[Cl-].[45Ca+2] UXVMQQNJUSDDNG-HDMMMHCHSA-L 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000004665 cationic fabric softener Substances 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 235000000484 citronellol Nutrition 0.000 description 1
- 229940071160 cocoate Drugs 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 1
- 229940019836 cyclamen aldehyde Drugs 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000003599 detergent Substances 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
- ZCPCLAPUXMZUCD-UHFFFAOYSA-M dihexadecyl(dimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCC ZCPCLAPUXMZUCD-UHFFFAOYSA-M 0.000 description 1
- 229940008099 dimethicone Drugs 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- XQRLCLUYWUNEEH-UHFFFAOYSA-N diphosphonic acid Chemical compound OP(=O)OP(O)=O XQRLCLUYWUNEEH-UHFFFAOYSA-N 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229940095139 ethylhexyl laurate Drugs 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229940050410 gluconate Drugs 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 229940033357 isopropyl laurate 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
- 230000002045 lasting effect Effects 0.000 description 1
- 235000009606 lavandin Nutrition 0.000 description 1
- 244000056931 lavandin Species 0.000 description 1
- SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 description 1
- 229930007744 linalool Natural products 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- FBUKVWPVBMHYJY-UHFFFAOYSA-M nonanoate Chemical compound CCCCCCCCC([O-])=O FBUKVWPVBMHYJY-UHFFFAOYSA-M 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000003068 static effect Effects 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
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- PJHKBYALYHRYSK-UHFFFAOYSA-N triheptanoin Chemical compound CCCCCCC(=O)OCC(OC(=O)CCCCCC)COC(=O)CCCCCC PJHKBYALYHRYSK-UHFFFAOYSA-N 0.000 description 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
- ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
-
- 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
-
- 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
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
-
- 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
- C11D3/50—Perfumes
Definitions
- the present invention relates to fabric softener compositions, in particular to fabric softener compositions comprising an aqueous phase and a hydrophobic phase.
- Fabric softeners for domestic use are primarily designed to give a pleasant feel to fabrics, to impart freshness or a pleasant smell, and to control the static electricity that impairs the comfort of handling and wearing clothes. They are generally aqueous dispersions containing a cationic softener as an active material. Fabric softener composition usually have a pH value below 4 due to the active material, i.e. the cationic softener, whereas detergents which contain mostly anionic surfactants as active ingredient have a pH value above 5, preferably above 7, more preferably about 9 to 10, depending on the application, e.g. fabric or skin.
- a known fabric softener composition is disclosed in WO 97/16516 comprising a cationic fabric softener, a fragrance, a non-ionic surfactant, a water-soluble ionisable inorganic salt and water.
- the fabric softener composition is in the form of an aqueous phase with discrete hydrophobic particles dispersed substantially uniformly throughout the aqueous phase.
- a problem with aqueous dispersions of this type is that the fragrance is mixed intimately with the other ingredients. Some of the ingredients, e.g. the cationic softener, tend to degrade fragrance over time. Also, the degradation of the fragrance is promoted by the aggressive acidic media, pH ⁇ 4, contained in such fabric softener compositions.
- a multiple-phase fabric care composition comprising visually distinct phases is disclosed in WO01/98450. Whereas fabric care agents including perfume are disclosed, the reference provides no teaching to the effect that perfume and cationic softener should be contained in separate phases.
- the invention provides in one of its aspects a fabric softener composition having an upper hydrophobic phase comprising a fragrance and a lower aqueous phase comprising a cationic softener wherein the pH value of the aqueous phase is below 4.
- compositions according to the present invention are possessed of numerous advantages.
- the fragrance is separated from aggressive media such as the cationic softener and accordingly, from the acidic aqueous phase which at a pH value below 4, particularly between 3 and 1, more particularly between 2.5 and 1, may act to degrade the fragrance, and as such, its effect is much longer lasting compared with fragrances employed in aqueous dispersion systems.
- the user is presented with an enhanced burst of fragrance upon opening a package, e.g. a bottle, containing a composition according to the present invention compared with aqueous dispersion systems wherein the fragrance is dispersed throughout the composition in a less concentrated manner.
- composition As the composition is provided as a two-phase system, it should be shaken prior to use to ensure good mixing of all the ingredients. However, because of the problem of fragrance degradation it is desirable that after use, the composition re-establishes its two-phase form as quickly as possible, and preferably separation into the distinct phases occurs within about 10 to about 40 minutes after agitation.
- Softeners for use in a composition according to the present invention may be selected from cationic softeners, more particular from the group of cationic quaternary ammonium salts; ester-linked quaternary ammonium compounds; imidazolinium salts; and amido amine salts. Particular examples of these cationic softeners are described in more details below.
- Quaternary ammonium compounds useful in the present invention may be selected from compounds of the formula: wherein each of R 1 and R 2 is independently selected from a hydrocarbon residue having from 8 to 28, preferably 2 to 24 carbon atoms; R 3 and R 4 represent hydrocarbon residues containing from 1 to 4 carbon atoms; and X' is an anion, which can be any suitable softener-compatible anion, for example, halide (preferably chloride or bromide), methylsulfate, ethylsulfate, formate, sulfate, nitrate, acetate and the like.
- halide preferably chloride or bromide
- quaternary ammonium compounds include ditallow dimethyl ammonium chloride, ditallow dimethyl ammonium methyl sulphate, dihexadecyl dimethyl ammonium chloride, di(hydrogenated tallow) dimethyl ammonium methyl sulphate, dihexadecyl diethyl ammonium chloride and di(coconut oil alkyl) dimethyl ammonium chloride.
- Suitable materials also include dialkyl ethoxyl methyl ammonium methosulphate based on soft fatty acids, dialkyl ethoxyl methyl ammonium methosulphate based on hard fatty acids, and compounds in which R 3 and R 4 represent methyl, R 2 is C 13-15 hydrocarbon group, R 3 is CH 2 CH 2 OCOR 5 where R 5 is stearyl, and X' is methylsulphate anion.
- Particular preferred cationic softener useful in the composition according to the invention can be an ester-linked quaternary ammonium compound represented by the formula: wherein each R 6 group is independently selected from C 1-6 hydrocarbon residue, such as alkyl, alkenyl or hydroxyalkyl groups; and wherein each R 7 group is independently selected from C 8-28 linear or branched hydrocarbon residue, such as alkyl or alkenyl groups; T is wherein R 8 represents hydrogen, methyl, or ethyl; n is an integer from 0-5 and m is an integer from 1-4; and X - is an anion as defined as above.
- a preferred material of ester-linked quaternary ammonium compound is that of formula: wherein each R 9 is a linear or branched alkyl or alkenyl chain comprising at least 11 atoms such as tallow and X - is an anion as defined above and, in particular, is methylsulfate.
- a compound having R 11 is tallow and X - is methylsulphate anion is available from Witco under the trade name Rewoquat® WE 18.
- Another example of this type of material is a compound wherein R 11 is of partially hardened tallow and X' is methylsulphate anion.
- R 10 is a linear or branched alkyl or alkenyl residue such as tallow, or partially hardened tallow and X - is an anion as herein above defined and in particular chloride or methylsulphate.
- ester-linked quaternary ammonium compounds which may be used in the compositions of the present invention, are those of the formula: wherein each R 11 is independently selected from C 1-4 hydrocarbon residue, such as alkyl, alkenyl or hydroxyalkyl groups; and each R 12 is independently selected from C 8-28 linear or branched hydrocarbon residue, such as alkyl and alkenyl groups; T has the meaning as described above; n is an integer of from 0-5 and m is an integer from 1-4; X - is an anion as defined above, preferably selected from halide, methylsulphate and ethylsulphate.
- the most preferred class of cationic softener is a biodegradable fatty ester quaternary ammonium compound of formula: wherein each R' 3 independently represents an aliphatic hydrocarbon residue having from 8 to 22 carbon atoms; R 14 represents (CH 2 ) s R 16 where R 16 represents an alkoxy carbonyl residue containing from 8 to 22 carbon atoms, benzyl, phenyl, C 1 -C 4 -alkyl substituted phenyl, OH or H; R 15 represents (CH 2 ) t R 17 where R 17 represents benzyl, phenyl, C 1 -C 4 -alkyl substituted phenyl, OH or H; q,r,s and t each independently, represent a number from 1 to 3; and X - is an anion as defined above, and the symbol "a" represents the ionic valance of the anion.
- R 18 is a hydrocarbon residue containing from 1 to 4, preferably 1 or 2 carbon atoms
- R 21 is a hydrocarbon residue containing from 8 to 25 carbon atoms
- R 19 is a linear or branched hydrocarbon residue containing from 8 to 25 carbon atoms
- R 20 is hydrogen or a hydrocarbon residue containing from 1 to 4 carbon atoms
- X - is an anion as defined above, and in particular a halide, methylsulphate or ethylsulphate.
- Preferred imidazolinium salts include 1-methyl-1-(tallowylamido-) ethyl-2-tallowyl-4,5-dihydroimidazolinium methosulphate and 1-methyl-1-(palmitoylamido) ethyl-2-octadecyl-4,5-dihydroimidazolinium chloride.
- Other useful imidazolinium materials are 2-heptadecyl-1-methyl-1-(2-stearylamido)-ethyl-imidazolinium chloride and 2-lauryl-1-hydroxyethyl-1-oleyl-imidazolinium chloride.
- ester-linked quaternary ammonium compounds show a reduced tendency as emulsifying agents compared with the other classes of cationic softener and thereby promote rapid separation of the composition into two distinct phases.
- Other advantages of these softeners are the good biodegradibility and their efficient softening results. Because of the aforementioned advantages, ester-linked quaternary ammonium compounds are preferred.
- Most preferred cationic softeners according to the present invention include Rewoquate® WE18 and Rewoquate WE15.
- the softener referred to hereinabove permit phase-separation within an acceptable time period, nevertheless they are surfactants and it is in the nature of surfactants to resist, to a certain extent, phase-separation and as such it is preferred to use as little cationic softener as possible.
- the cationic softener is needed to impart softness to fabrics and so one has to strike a balance between the need for rapid phase separation and the competitive need for acceptable fabric softness. It is within the realm of routine experimentation for the skilled person to find an appropriate balance having regard to these competing factors.
- it is preferred to use in the composition according to the present invention about 1 % to about 18 % (w/w) of a cationic softener, preferably 2 % to 13 %, more preferably 5% to 10% (w/w).
- Non-ionic surfactants are used in fabric softener compositions of the prior art for example, in combination with cationic softeners. However, we have found that non-ionic surfactants promote emulsification to an extent that phase separation is not quickly established using these materials. Accordingly, it is preferred to avoid the use of non-ionic surfactants in compositions of the present invention.
- compositions according to the present invention preferably comprise up to 2%(w/w), more preferably up to 1%, most preferably up to 0.5% salts.
- Preferred inorganic salts include alkali and alkaline earth halides, e.g. Mg-, Na-, Li-, Ca-, K-, and Al-halides, alkali and alkaline earth nitrates, sulphates, phosphates and silicates; including hydrates of these salts, and mixtures thereof.
- alkali and alkaline earth halides e.g. Mg-, Na-, Li-, Ca-, K-, and Al-halides, alkali and alkaline earth nitrates, sulphates, phosphates and silicates; including hydrates of these salts, and mixtures thereof.
- Preferred organic salts include alkali and alkaline earth salts of the carboxylic acids including formate, acetate, propionate, pelargonate, citrate, gluconate and lactate aromatic acids.
- excipients optionally present in the aqueous phase are anti-foaming agents, thickeners, fluorescent whitening agents, optical brightening agents, anti-wrinkling agents, anti-shrinking agents, sunscreens, colour care agents, colorants, ironing aids.
- the fabric softener composition according to the present invention comprise up to 8 % (w/w) of these other excipients, preferably from 2 % to 5 % (w/w).
- the hydrophobic phase according to the present of the invention comprises an oil and fragrance.
- oils are preferred wherein the HLB (hydrophilic-lipophilic balance) is below 5, more preferably between 4 and 1.
- the oil may be a hydrocarbon oil, for example a mixture of hydrocarbon oils obtained from petroleum, in particular petroleum jelly or for example Isopar® produced by Exxon, in particular Isopar® L, Isopar® M or Isopar® H.
- oils such as dimethicone polysiloxane or Tegopren®; or ester oil such as isopropylmyristate, ethylhexyl laurate, isopropyl laurate, octyl adipate and ethylhexyl cocoate. Mixtures of ester oil, hydrocarbon oil and silicone oil may also be used. Because of environmental reasons biodegradable oils are preferred. Accordingly, most preferred oils are esters oils, for example isopropylmyristate, isopropylpalmitate, neopentyl glycol diethylhexanoate, glycerol trioleate or glyceryl triheptanoate. To avoid alteration of the characteristic of the fragrance by the oil, such oils are preferred, which have a low evaporation rate.
- the fabric softener composition according to the present invention comprises 1 % to 50 % (w/w) of the hydrophobic phase, preferably 3 % to 20 % (w/w), and most preferred 5 % to 12 % (w/w).
- the oil may also treat a fabric to impart softness thereto. Accordingly, the presence of the oil may have the beneficial effect of permitting the use of less cationic softener which is relatively expensive compared with the oil.
- the oil may coat the fragrance, such that when the composition is applied to a fabric it tends to promote prolonged release of fragrance and so increasing the substantivity of the fragrance on the fabric, for example preferred compositions according to the invention may impart fragrance to a fabric for up to 7 days after treatment. It was found that the rinse loss of the fragrance during the rinse cycle and/or the fragrance lost during the tumble drying process is much lower compared with aqueous dispersion fabric softeners. On dry fabrics a 3 - 5 time stronger fragrance, measured by headspace, can be achieved compared with conventional aqueous dispersion fabric softeners. The headspace analysis is described in the Journal of Agriculture and Food Chemistry, Vol. 19, No. 6 (1971), page 1049-1056.
- the composition according to the present invention may contain all kinds of fragrances of natural and/or synthetic origin, for example geraniol, citronellyl acetate, d-limonene, orange terpenes and vanilline.
- the composition comprises one fragrance or a mixture of fragrances.
- water soluble fragrances are preferably to be avoided.
- the aqueous solubility of a fragrance is conventionally measured using a number of different procedures such as for example the procedure disclosed in Etzweiler et al., Analytical Chemistry, Vol.
- fragrances have a aqueous solubility below 20000 ppm, preferably below 10000 ppm, more preferably below 5000 ppm, most preferably below 2000 ppm.
- fragrances such as phenylethylalcohol and diethylmalonate are preferably to be avoided.
- preferred fragrances have a clogP greater than 2, most preferred a clogP greater than 3.
- the composition according to the present invention comprises about 0.1 % to about 3 %(w/w) fragrance.
- fragrance compositions having at least 80 % (w/w) of fragrance with a clogP greater than 2.
- the hydrophobic phase may comprise a lipophilic dye, for example Puricolor® blue FBL5, Puricolor® blue FBL5 Puricolor® blue ABL9, Puricolor® green U3 or Puricolor® yellow AYE23 from Ciba.
- a lipophilic dye for example Puricolor® blue FBL5, Puricolor® blue FBL5 Puricolor® blue ABL9, Puricolor® green U3 or Puricolor® yellow AYE23 from Ciba.
- a preferred composition according to the present invention comprises from 2% to 18% (w/w) of cationic softener; from 1% to 50% (w/w) of oil; from 0,1% to 3% (w/w) of fragrance; and from 29% to 96,9% (w/w) of water.
- composition according to the present invention comprises from 2 % to 15 % (w/w) cationic softener; from 3 % to 20 % (w/w) ester oil; from 0.1 % to 3 % (w/w) fragrance; from 57 % to 92.9 % (w/w) water; and from 2 % to 5 % (w/w) other excipients.
- compositions according to the present invention may be used as fabric softeners. They may be added to the last rinse cycle in an amount of 35 ml to 150 ml per 4 kg of fabrics in general, or garments in particular. However, the amounts used is based upon the preferences of the user.
- a fabric softening composition of the present invention (herein after named as "bi-phase fabric softener”) was formulated as follows: % wlw Part A Rewoquat® WE 18 (Goldschmidt) di-(tallow carboxyethyl) hydroxy-ethyl methylammonium methosulfate 10.00 Deionised Water 74.45 Calcium chloride 0.50 Myacide® BT330 (Boots) 2-bromo-2-nitropropane-1,3-diol 0.05 Part B Isopropylmyristate 11.50 IsoparTM M (Exxon) 2.50 Fragrance 1.00 100.00
- the water and the Rewoquat® WE 18 was heated separately to 50°C. While stirring the preheated water, one half of the Rewoquat® WE 18 (preheated to 50°C) was added. Calcium chloride was added and then the remaining part of the Rewoquat® WE 18 while stirring the mixture. After cooling to room temperature under stirring, Myacide® BT330 was added. Finally, part B was added.
- the bi-phase fabric softener composition prepared according to example 1 was compared to a mono-phase fabric softener composition formulated as follows: % w/w Part A Deionised Water 81.75 MgCl 2 (saturated solution) 1.0 Part B Rewoquat® WE 18 (Goldschmidt) di-(tallow carboxyethyl) hydroxy-ethyl methylammonium methosulfate 13.0 GenapolO100 (Hoescht) Ethoxylated fatty alcohol C16 - C18 10EO 2.0 Antifoam 110A-EU (Dow Corning) silicone emulsion 1.0 Part C Dequest 2010 (Monsanto) Hydroxyethyliden 1,1 diphosphonic acid 0.2 Proxel GXL (ICI) Benzisothiazolinone sodium salt 0.02 Bronidox L (Cognis) 5 bromo-5nitro-1,3 Dioxane 0.03 Fragrance 1.0 100.00
- part A was heated to 65°C. Then part B (preheated to 65°C) was added while stirring the mixture. After cooling to room temperature part C was added.
- the cotton terry towels were washed according to the washing protocol of example 2.
- the towels were line dried and placed in a glass container 1 day / 5 days after drying. During 15 minutes and an extraction flow of 30l/minute the headspace was collected. Then the samples were analysed by GC/MS. The results are shown in Table 2.
- the bi-phase fabric softener delivered significantly more fragrance on the cotton terry towels.
Claims (12)
- Composition de produit assouplissant ayant une phase hydrophobe supérieure comprenant un parfum et une phase aqueuse inférieure comprenant un agent assouplissant cationique, dans laquelle le pH de la phase aqueuse est inférieur à 4.
- Composition de produit assouplissant selon la revendication 1, dans laquelle l'agent assouplissant cationique est choisi parmi le groupe des sels d'imidazolinium; des amidoamines et des sels d'ammonium quaternaire à liaison ester.
- Composition de produit assouplissant selon les revendications 1 et 2, comprenant jusqu'à 18% (p/p) d'agent assouplissant cationique.
- Composition de produit assouplissant selon l'une quelconque des revendications précédentes, dans laquelle l'huile est choisie parmi la liste suivante: huile hydrocarbonée, huile de silicone et huile d'ester.
- Composition de produit assouplissant selon la revendication 4, comprenant une huile hydrocarbonée, une huile de silicone ou une huile d'ester avec un équilibre hydrophile-lipophile inférieur à 5.
- Composition de produit assouplissant selon l'une quelconque des revendications précédentes, comprenant de 1 % à 50% (p/p) d'huile.
- Composition de produit assouplissant selon la revendication 1, comprenant:de 2% à 18% (p/p) d'agent assouplissant cationique;de 1% à 50% (p/p) d'huile;de 0,1 % à 3% (p/p) de parfum; etde 29% à 96,9% (p/p) d'eau.
- Composition de produit assouplissant selon l'une quelconque des revendications précédentes, dans laquelle le parfum est caractérisé par un clogP supérieur à 2, de préférence un clogP supérieur à 3.
- Composition de produit assouplissant selon l'une quelconque des revendications précédentes, adaptée pour se disperser après agitation, dans laquelle la dispersion se sépare en une phase hydrophile et en une phase aqueuse environ 10 à environ 40 minutes après l'agitation.
- Procédé pour prolonger la libération d'un parfum à partir d'un tissu jusqu'à 7 jours, comprenant l'étape qui consiste à traiter un tissu avec une composition telle que décrite dans l'une quelconque des revendications précédentes.
- Composition de produit assouplissant conditionnée, caractérisée par une phase hydrophobe supérieure comprenant un parfum et une phase aqueuse inférieure comprenant un agent assouplissant cationique, dans laquelle la phase aqueuse a un pH inférieur à 4.
- Composition de produit assouplissant conditionnée selon la revendication 11, comprenant:de 2% à 18% (p/p) d'agent assouplissant cationique;de 1% à 50% (p/p) d'huile;de 0,1 % à 3% (p/p) de parfum ; etde 29% à 96,9% (p/p) d'eau.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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EP02745044A EP1412467B1 (fr) | 2001-07-27 | 2002-07-25 | Composition adoucissante pour tissu |
Applications Claiming Priority (4)
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EP01118341A EP1279726A1 (fr) | 2001-07-27 | 2001-07-27 | Compositions adoucissantes |
EP01118341 | 2001-07-27 | ||
PCT/CH2002/000420 WO2003012022A1 (fr) | 2001-07-27 | 2002-07-25 | Composition adoucissante pour tissu |
EP02745044A EP1412467B1 (fr) | 2001-07-27 | 2002-07-25 | Composition adoucissante pour tissu |
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EP1412467A1 EP1412467A1 (fr) | 2004-04-28 |
EP1412467B1 true EP1412467B1 (fr) | 2005-11-23 |
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EP01118341A Withdrawn EP1279726A1 (fr) | 2001-06-27 | 2001-07-27 | Compositions adoucissantes |
EP02745044A Expired - Lifetime EP1412467B1 (fr) | 2001-07-27 | 2002-07-25 | Composition adoucissante pour tissu |
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EP01118341A Withdrawn EP1279726A1 (fr) | 2001-06-27 | 2001-07-27 | Compositions adoucissantes |
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EP (2) | EP1279726A1 (fr) |
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AT (1) | ATE310798T1 (fr) |
DE (1) | DE60207577T2 (fr) |
ES (1) | ES2252480T3 (fr) |
WO (1) | WO2003012022A1 (fr) |
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CN104284972A (zh) * | 2012-05-17 | 2015-01-14 | 高露洁-棕榄公司 | 多相表面活性剂香料组合物 |
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KR100828021B1 (ko) * | 2001-11-07 | 2008-05-08 | 주식회사 엘지생활건강 | 섬유유연제 조성물 |
US20040097396A1 (en) * | 2002-11-14 | 2004-05-20 | Myriam Peeters | Concentrated fabric softening composition containing esterquat with specific ester distribution and an electrolyte |
US20040097395A1 (en) * | 2002-11-14 | 2004-05-20 | Andre Crutzen | Fabric softening composition containing esterquat with specific ester distribution and sequestrant |
GB2419361A (en) * | 2004-10-20 | 2006-04-26 | Reckitt Benckiser | Fabric softener comprising a sublimable carrier |
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JP5210360B2 (ja) * | 2009-07-30 | 2013-06-12 | ローム アンド ハース カンパニー | 相乗的殺微生物組成物 |
WO2011154926A1 (fr) * | 2010-06-10 | 2011-12-15 | Firmenich Sa | Compositions de parfums et leurs utilisations |
CN103380205B (zh) | 2010-12-03 | 2015-11-25 | 荷兰联合利华有限公司 | 织物调理剂 |
CN103228774A (zh) * | 2010-12-03 | 2013-07-31 | 荷兰联合利华有限公司 | 织物调理剂 |
DE102012220466A1 (de) * | 2012-11-09 | 2014-05-15 | Henkel Ag & Co. Kgaa | Textilpflegemittel |
US9340757B2 (en) | 2013-04-18 | 2016-05-17 | The Procter & Gamble Company | Fragrance materials |
MX2018007504A (es) * | 2015-12-28 | 2018-08-01 | Colgate Palmolive Co | Composiciones suavizantes de telas. |
GB2547685A (en) * | 2016-02-26 | 2017-08-30 | Reckitt Benckiser Laundry Detergents | Composition |
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CA783534A (en) * | 1965-06-15 | 1968-04-23 | Unilever Limited | Liquid detergent compositions |
GB8827698D0 (en) * | 1988-11-28 | 1988-12-29 | Unilever Plc | Fabric-treatment composition |
GB9403242D0 (en) * | 1994-02-21 | 1994-04-13 | Unilever Plc | Fabric softening composition |
GB9617612D0 (en) * | 1996-08-22 | 1996-10-02 | Unilever Plc | Fabric conditioning composition |
GB9804283D0 (en) * | 1998-02-27 | 1998-04-22 | Unilever Plc | Fabric conditioning concentrate |
CN1214149C (zh) * | 1999-05-21 | 2005-08-10 | 荷兰联合利华有限公司 | 织物柔软组合物 |
DE19936727A1 (de) * | 1999-08-06 | 2001-02-08 | Henkel Kgaa | Niotensidbasiertes wäßriges mehrphasiges Reinigungsmittel |
DE19945503A1 (de) * | 1999-09-23 | 2001-04-05 | Henkel Kgaa | Mehrphasiges Reinigungsmittel mit antimikrobieller Wirkung |
DE20014021U1 (de) * | 2000-07-27 | 2001-01-11 | Henkel Kgaa | Textilreinigungskit |
-
2001
- 2001-07-27 EP EP01118341A patent/EP1279726A1/fr not_active Withdrawn
-
2002
- 2002-07-25 US US10/484,225 patent/US20050049173A1/en not_active Abandoned
- 2002-07-25 AT AT02745044T patent/ATE310798T1/de not_active IP Right Cessation
- 2002-07-25 ES ES02745044T patent/ES2252480T3/es not_active Expired - Lifetime
- 2002-07-25 DE DE60207577T patent/DE60207577T2/de not_active Expired - Fee Related
- 2002-07-25 KR KR10-2004-7001147A patent/KR20040018519A/ko not_active Application Discontinuation
- 2002-07-25 WO PCT/CH2002/000420 patent/WO2003012022A1/fr not_active Application Discontinuation
- 2002-07-25 EP EP02745044A patent/EP1412467B1/fr not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104284972A (zh) * | 2012-05-17 | 2015-01-14 | 高露洁-棕榄公司 | 多相表面活性剂香料组合物 |
CN104284972B (zh) * | 2012-05-17 | 2017-08-04 | 高露洁-棕榄公司 | 多相表面活性剂香料组合物 |
Also Published As
Publication number | Publication date |
---|---|
ATE310798T1 (de) | 2005-12-15 |
US20050049173A1 (en) | 2005-03-03 |
ES2252480T3 (es) | 2006-05-16 |
KR20040018519A (ko) | 2004-03-03 |
WO2003012022A1 (fr) | 2003-02-13 |
DE60207577T2 (de) | 2006-07-27 |
EP1279726A1 (fr) | 2003-01-29 |
DE60207577D1 (de) | 2005-12-29 |
EP1412467A1 (fr) | 2004-04-28 |
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