EP3047011B1 - Use of alkyl-/ alkenyl-oligoglycoside derivatives for treating textiles - Google Patents
Use of alkyl-/ alkenyl-oligoglycoside derivatives for treating textiles Download PDFInfo
- Publication number
- EP3047011B1 EP3047011B1 EP14765940.3A EP14765940A EP3047011B1 EP 3047011 B1 EP3047011 B1 EP 3047011B1 EP 14765940 A EP14765940 A EP 14765940A EP 3047011 B1 EP3047011 B1 EP 3047011B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- alkyl
- alkenyl
- agents
- oder
- bis
- 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.)
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- 239000004753 textile Substances 0.000 title claims description 107
- 125000000217 alkyl group Chemical group 0.000 claims description 75
- 239000003795 chemical substances by application Substances 0.000 claims description 66
- 238000011282 treatment Methods 0.000 claims description 65
- -1 pH adjusters Substances 0.000 claims description 57
- 125000003342 alkenyl group Chemical group 0.000 claims description 54
- 125000004432 carbon atom Chemical group C* 0.000 claims description 34
- 239000003945 anionic surfactant Substances 0.000 claims description 27
- 239000003599 detergent Substances 0.000 claims description 26
- 150000007942 carboxylates Chemical class 0.000 claims description 24
- 150000001875 compounds Chemical class 0.000 claims description 21
- 229910019142 PO4 Inorganic materials 0.000 claims description 19
- 235000021317 phosphate Nutrition 0.000 claims description 19
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical class OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 claims description 17
- 239000002736 nonionic surfactant Substances 0.000 claims description 13
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 13
- 102000004190 Enzymes Human genes 0.000 claims description 11
- 108090000790 Enzymes Proteins 0.000 claims description 11
- 239000000975 dye Substances 0.000 claims description 10
- 239000003112 inhibitor Substances 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 8
- 150000001323 aldoses Chemical class 0.000 claims description 6
- 239000002304 perfume Substances 0.000 claims description 6
- 229910052700 potassium Inorganic materials 0.000 claims description 6
- 229910052708 sodium Inorganic materials 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 238000002845 discoloration Methods 0.000 claims description 5
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 4
- 208000007976 Ketosis Diseases 0.000 claims description 4
- 239000003125 aqueous solvent Substances 0.000 claims description 4
- 239000008103 glucose Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 150000002584 ketoses Chemical class 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 239000007844 bleaching agent Substances 0.000 claims description 3
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 230000002579 anti-swelling effect Effects 0.000 claims description 2
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 239000002216 antistatic agent Substances 0.000 claims description 2
- 239000000969 carrier Substances 0.000 claims description 2
- 239000008139 complexing agent Substances 0.000 claims description 2
- 230000007797 corrosion Effects 0.000 claims description 2
- 238000005260 corrosion Methods 0.000 claims description 2
- 238000004042 decolorization Methods 0.000 claims description 2
- 239000003792 electrolyte Substances 0.000 claims description 2
- 239000000417 fungicide Substances 0.000 claims description 2
- 230000002070 germicidal effect Effects 0.000 claims description 2
- 238000010409 ironing Methods 0.000 claims description 2
- 239000003755 preservative agent Substances 0.000 claims description 2
- 229920002545 silicone oil Polymers 0.000 claims description 2
- 125000000524 functional group Chemical group 0.000 claims 3
- 125000003563 glycoside group Chemical group 0.000 claims 2
- 239000006096 absorbing agent Substances 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 230000000845 anti-microbial effect Effects 0.000 claims 1
- 230000003165 hydrotropic effect Effects 0.000 claims 1
- 239000012748 slip agent Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 37
- 150000002338 glycosides Chemical group 0.000 description 19
- 229930182470 glycoside Natural products 0.000 description 18
- 239000007788 liquid Substances 0.000 description 17
- 150000002191 fatty alcohols Chemical class 0.000 description 16
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 15
- 230000009021 linear effect Effects 0.000 description 14
- CZMRCDWAGMRECN-UHFFFAOYSA-N 2-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound OCC1OC(CO)(OC2OC(CO)C(O)C(O)C2O)C(O)C1O CZMRCDWAGMRECN-UHFFFAOYSA-N 0.000 description 13
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 13
- 239000002253 acid Substances 0.000 description 12
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 150000001768 cations Chemical class 0.000 description 11
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 10
- 238000004140 cleaning Methods 0.000 description 10
- 235000014113 dietary fatty acids Nutrition 0.000 description 10
- 229940088598 enzyme Drugs 0.000 description 10
- 239000000194 fatty acid Substances 0.000 description 10
- 229930195729 fatty acid Natural products 0.000 description 10
- 239000010452 phosphate Substances 0.000 description 10
- 229920001296 polysiloxane Polymers 0.000 description 10
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- 150000004665 fatty acids Chemical class 0.000 description 9
- 239000003760 tallow Substances 0.000 description 9
- 150000007513 acids Chemical class 0.000 description 8
- 125000001931 aliphatic group Chemical group 0.000 description 8
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 8
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- 239000004435 Oxo alcohol Substances 0.000 description 5
- 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 5
- 150000004820 halides Chemical class 0.000 description 5
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 229940085991 phosphate ion Drugs 0.000 description 5
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 5
- 125000000923 (C1-C30) alkyl group Chemical group 0.000 description 4
- 102000013142 Amylases Human genes 0.000 description 4
- 108010065511 Amylases Proteins 0.000 description 4
- 235000013162 Cocos nucifera Nutrition 0.000 description 4
- 244000060011 Cocos nucifera Species 0.000 description 4
- 108091005804 Peptidases Proteins 0.000 description 4
- 239000004365 Protease Substances 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 235000019418 amylase Nutrition 0.000 description 4
- 150000001450 anions Chemical class 0.000 description 4
- 229960000541 cetyl alcohol Drugs 0.000 description 4
- 230000003750 conditioning effect Effects 0.000 description 4
- 238000004043 dyeing Methods 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 239000002979 fabric softener Substances 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229940043348 myristyl alcohol Drugs 0.000 description 4
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 4
- 229940012831 stearyl alcohol Drugs 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- 239000004367 Lipase Substances 0.000 description 3
- 102000004882 Lipase Human genes 0.000 description 3
- 108090001060 Lipase Proteins 0.000 description 3
- 102000035195 Peptidases Human genes 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 3
- 229920006317 cationic polymer Polymers 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 239000012459 cleaning agent Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000005562 fading Methods 0.000 description 3
- 239000003925 fat Substances 0.000 description 3
- 235000019197 fats Nutrition 0.000 description 3
- 235000019421 lipase Nutrition 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229910052901 montmorillonite Inorganic materials 0.000 description 3
- 238000006384 oligomerization reaction Methods 0.000 description 3
- 229920000058 polyacrylate Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- 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
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 2
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- 239000004382 Amylase Substances 0.000 description 2
- 102100032487 Beta-mannosidase Human genes 0.000 description 2
- 108010059892 Cellulase Proteins 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 229910003849 O-Si Inorganic materials 0.000 description 2
- 102000004316 Oxidoreductases Human genes 0.000 description 2
- 108090000854 Oxidoreductases Proteins 0.000 description 2
- 229910003872 O—Si Inorganic materials 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000004902 Softening Agent Substances 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000008051 alkyl sulfates Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 229940025131 amylases Drugs 0.000 description 2
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 2
- 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 2
- 108010055059 beta-Mannosidase Proteins 0.000 description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 2
- 229940106157 cellulase Drugs 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 125000002704 decyl 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])* 0.000 description 2
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
- LIWAQLJGPBVORC-UHFFFAOYSA-N ethylmethylamine Chemical compound CCNC LIWAQLJGPBVORC-UHFFFAOYSA-N 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 229930182478 glucoside Natural products 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 108010002430 hemicellulase Proteins 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 125000002960 margaryl 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])[H] 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 125000001196 nonadecyl 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])C([H])([H])[H] 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 125000002958 pentadecyl 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])[H] 0.000 description 2
- 229920005646 polycarboxylate Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 150000003138 primary alcohols Chemical class 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
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- 239000007787 solid Substances 0.000 description 2
- 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 2
- 238000003860 storage Methods 0.000 description 2
- 238000006277 sulfonation reaction Methods 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 1
- NPMRPDRLIHYOBW-UHFFFAOYSA-N 1-(2-butoxyethoxy)propan-2-ol Chemical compound CCCCOCCOCC(C)O NPMRPDRLIHYOBW-UHFFFAOYSA-N 0.000 description 1
- QWOZZTWBWQMEPD-UHFFFAOYSA-N 1-(2-ethoxypropoxy)propan-2-ol Chemical compound CCOC(C)COCC(C)O QWOZZTWBWQMEPD-UHFFFAOYSA-N 0.000 description 1
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 1
- JOLQKTGDSGKSKJ-UHFFFAOYSA-N 1-ethoxypropan-2-ol Chemical compound CCOCC(C)O JOLQKTGDSGKSKJ-UHFFFAOYSA-N 0.000 description 1
- FENFUOGYJVOCRY-UHFFFAOYSA-N 1-propoxypropan-2-ol Chemical compound CCCOCC(C)O FENFUOGYJVOCRY-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- COBPKKZHLDDMTB-UHFFFAOYSA-N 2-[2-(2-butoxyethoxy)ethoxy]ethanol Chemical compound CCCCOCCOCCOCCO COBPKKZHLDDMTB-UHFFFAOYSA-N 0.000 description 1
- WFSMVVDJSNMRAR-UHFFFAOYSA-N 2-[2-(2-ethoxyethoxy)ethoxy]ethanol Chemical compound CCOCCOCCOCCO WFSMVVDJSNMRAR-UHFFFAOYSA-N 0.000 description 1
- MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- IFBPWBDEENYUEG-UHFFFAOYSA-N 2-hydroxyethyl-methyl-bis(2-octadecanoyloxyethyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC[N+](C)(CCO)CCOC(=O)CCCCCCCCCCCCCCCCC IFBPWBDEENYUEG-UHFFFAOYSA-N 0.000 description 1
- XEEYSDHEOQHCDA-UHFFFAOYSA-N 2-methylprop-2-ene-1-sulfonic acid Chemical compound CC(=C)CS(O)(=O)=O XEEYSDHEOQHCDA-UHFFFAOYSA-N 0.000 description 1
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 description 1
- YEYKMVJDLWJFOA-UHFFFAOYSA-N 2-propoxyethanol Chemical compound CCCOCCO YEYKMVJDLWJFOA-UHFFFAOYSA-N 0.000 description 1
- QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical compound COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- 108700038091 Beta-glucanases Proteins 0.000 description 1
- RBPBNPQIFLJCDH-UHFFFAOYSA-N C(C)OC(COCCO)(CCCC)CCCC Chemical compound C(C)OC(COCCO)(CCCC)CCCC RBPBNPQIFLJCDH-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 108010084185 Cellulases Proteins 0.000 description 1
- 102000005575 Cellulases Human genes 0.000 description 1
- RUPBZQFQVRMKDG-UHFFFAOYSA-M Didecyldimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCCCCCCCCC RUPBZQFQVRMKDG-UHFFFAOYSA-M 0.000 description 1
- 101710121765 Endo-1,4-beta-xylanase Proteins 0.000 description 1
- 229910004646 HP 56 K Inorganic materials 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 108010059820 Polygalacturonase Proteins 0.000 description 1
- 229920000289 Polyquaternium Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 238000005904 alkaline hydrolysis reaction Methods 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000005741 alkyl alkenyl group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
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- 102000004139 alpha-Amylases Human genes 0.000 description 1
- 108090000637 alpha-Amylases Proteins 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 235000012216 bentonite Nutrition 0.000 description 1
- 108010047754 beta-Glucosidase Proteins 0.000 description 1
- 102000006995 beta-Glucosidase Human genes 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- VNSBYDPZHCQWNB-UHFFFAOYSA-N calcium;aluminum;dioxido(oxo)silane;sodium;hydrate Chemical compound O.[Na].[Al].[Ca+2].[O-][Si]([O-])=O VNSBYDPZHCQWNB-UHFFFAOYSA-N 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000003982 chlorocarboxylic acids Chemical class 0.000 description 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
- 229960001231 choline Drugs 0.000 description 1
- 229940096386 coconut alcohol Drugs 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 239000008406 cosmetic ingredient Substances 0.000 description 1
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 1
- 229960004670 didecyldimethylammonium chloride Drugs 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
- 229960000735 docosanol Drugs 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- COHIUILBPQNABR-UHFFFAOYSA-N dodecyl phenylmethanesulfonate;sodium Chemical group [Na].CCCCCCCCCCCCOS(=O)(=O)CC1=CC=CC=C1 COHIUILBPQNABR-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 108010093305 exopolygalacturonase Proteins 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 150000008131 glucosides Chemical class 0.000 description 1
- 239000000118 hair dye Substances 0.000 description 1
- KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 description 1
- 229910000271 hectorite Inorganic materials 0.000 description 1
- 229940059442 hemicellulase Drugs 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 229940094522 laponite Drugs 0.000 description 1
- 229940048848 lauryl glucoside Drugs 0.000 description 1
- 229940040461 lipase Drugs 0.000 description 1
- XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000005528 methosulfate group Chemical group 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- CXHHBNMLPJOKQD-UHFFFAOYSA-N methyl hydrogen carbonate Chemical compound COC(O)=O CXHHBNMLPJOKQD-UHFFFAOYSA-N 0.000 description 1
- 229940100573 methylpropanediol Drugs 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- ALQWDAJTEFASRJ-UHFFFAOYSA-N n-hexadecylhexadecan-1-amine;hydrochloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[NH2+]CCCCCCCCCCCCCCCC ALQWDAJTEFASRJ-UHFFFAOYSA-N 0.000 description 1
- 229910000273 nontronite Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- UMSVPCYSAUKCAZ-UHFFFAOYSA-N propane;hydrochloride Chemical compound Cl.CCC UMSVPCYSAUKCAZ-UHFFFAOYSA-N 0.000 description 1
- 235000019419 proteases Nutrition 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 229910000275 saponite Inorganic materials 0.000 description 1
- 229910000276 sauconite Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- FDRCDNZGSXJAFP-UHFFFAOYSA-M sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
- OPVVJRSLPIWLLG-UHFFFAOYSA-N sodium;phosphorous acid Chemical compound [Na+].OP(O)O OPVVJRSLPIWLLG-UHFFFAOYSA-N 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 108010038851 tannase Proteins 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/83—Mixtures of non-ionic with anionic 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
- C11D3/0021—Dye-stain or dye-transfer inhibiting compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
-
- 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
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- 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
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/12—Soft surfaces, e.g. textile
Definitions
- the invention relates to the technical field of textile treatment.
- the use of alkyl / alkenyl oligoglycoside derivatives in textile treatment agents, suitable agents and processes for treating textiles is described.
- surfactants are known for cleaning textiles, which can remove all types of soiling from the textile in an aqueous liquor.
- Surfactants serve as washing-active substances to increase the solubility in water, among other things, of fat and dirt particles that adhere to the laundry.
- the performance of such agents on fatty soiling is not always optimal, which leads to consumer dissatisfaction.
- dyes from a textile fiber e.g. of a wash item and transferred to the fleet it is possible that, e.g. in the presence of differently colored textiles in the laundry during the textile treatment, not only does color fading take place, but these textiles are also discolored by the dyes that have passed into the liquor.
- the dye transfer of dyes in the fleet e.g. on the textiles in the laundry must therefore be prevented or at least minimized.
- color transfer inhibitors such as, for example, polymers or copolymers of N-vinylimidazole, which lead to flocculation, precipitation or phase separation of the detergent, particularly when formulating liquid detergents.
- color transfer inhibitors which are sufficiently compatible with anionic surfactants.
- JP H04 327521 A describes detergent compositions containing an anionic glycoside derivative and excellent foam and cleaning properties show no irritation to skin or hair and are therefore proposed as detergents for skin, hair, textiles or food.
- the object of the present invention is to provide components for agents for textile treatment, in particular for the treatment of dyed textiles, which optimize or restrict the color retention of textiles, in particular the decolorization of the textiles and the discoloration of the textiles as part of a textile treatment. If these components are incorporated into, in particular, liquid preparations, the preparations should be stable in storage. If these components are incorporated into detergent, the detergent should have at least the same or better cleaning performance, in particular primary detergency.
- alkyl and / or alkenyl oligoglycoside carboxylates, sulfates, phosphates and / or isoethionates leads to improved color stability of dyed textiles. In particular, the fading of the textile color and the discoloration of textiles are reduced or prevented. If said alkyl and / or alkenyl oligoglycosides are used in detergents, the cleaning performance of the detergent, in particular the primary detergency, is additionally improved. When used in liquid compositions, in particular liquid detergents, the storage stability of the composition is increased compared to conventional color transfer inhibitors.
- textile treatment agents in particular detergents or fabric softeners, to improve the color stability of dyed textiles treated with them, in particular to reduce or avoid discoloration or discoloration of dyed textiles treated with them.
- At least one OH group of the radical G according to formula (I) is particularly preferably replaced by a group -O-CH 2 -COONa.
- the aldoses are preferably used.
- glucose is particularly suitable because of its easy accessibility and technical availability.
- the alkyl glycosides which are particularly preferably used as starting materials are therefore the alkyl glucosides.
- the alkyl radical R is derived from primary alcohols having 6 to 22, preferably 12 to 18, carbon atoms. Typical examples are capronic alcohol, caprylic alcohol, capric alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol and behenyl alcohol as well as technical fractions which, in addition to the saturated alcohols mentioned, can also contain proportions of unsaturated alcohols and which are based on natural fats and oils, for example palm oil, palm kernel oil, coconut oil or beef tallow can be obtained. The use of technical coconut alcohol is particularly preferred.
- the alkyl glycosides can also be derived from synthetic primary alcohols having 6 to 22 carbon atoms, in particular the so-called oxo alcohols, which have a proportion of 5 to 40% by weight of branched isomers.
- alkyl radicals are those with 8/10, 12/14, 8 to 16, 12 to 16 or 16 to 18 carbon atoms. Mixtures of the alkyl residues result from natural fats and oils or mineral oils.
- hydroxyl groups can also be etherified, for example.
- the textile treatment agents described can advantageously additionally contain anionic and / or further nonionic surfactants in order to optimize the cleaning performance.
- Suitable anionic surfactants include, but are not limited to, alkyl benzene sulfonates, olefin sulfonates, alkane sulfonates, fatty alcohol sulfates, fatty alcohol ether sulfates, or a mixture of two or more of these anionic surfactants. Of these anionic surfactants, alkylbenzenesulfonates, fatty alcohol ether sulfates and mixtures thereof are particularly preferred. Other suitable anionic surfactants are soaps, ie salts of fatty acids, especially those Na or K salts of C 12-18 fatty acids. Soaps can have a particularly beneficial effect on the cold washing performance.
- the surfactants of the sulfonate type are preferably alkylbenzenesulfonates, olefin sulfonates, ie mixtures of alkene and hydroxyalkanesulfonates and disulfonates such as are obtained, for example, from C 12-18 monoolefins with terminal or internal double bonds by sulfonation with gaseous sulfur trioxide and subsequent alkaline or acidic Hydrolysis of the sulfonation products is considered.
- Alkylbenzenesulfonates are preferably selected from linear or branched alkylbenzenesulfonates of the formula in which R 'and R "are independently H or alkyl and together contain 9 to 19, preferably 9 to 15 and in particular 9 to 13 carbon atoms.
- R 'and R "are independently H or alkyl and together contain 9 to 19, preferably 9 to 15 and in particular 9 to 13 carbon atoms.
- a very particularly preferred representative is sodium dodecylbenzyl sulfonate.
- the alk (en) yl sulfates are the salts of the sulfuric acid half-esters of the C 12 -C 18 fatty alcohols, for example from coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol or the C 10 -C 20 oxo alcohols and those half-esters secondary alcohols of these chain lengths are preferred.
- the C 12 -C 16 alkyl sulfates and C 12 -C 15 alkyl sulfates as well as C 14 -C 15 alkyl sulfates are preferred from the point of view of washing technology. 2,3-Alkyl sulfates are also suitable anionic surfactants.
- alkyl ether sulfates with the formula R 1 -O- (AO) n -SO 3 - X + are suitable.
- R 1 represents a linear or branched, substituted or unsubstituted alkyl radical, preferably a linear, unsubstituted alkyl radical, particularly preferably a fatty alcohol radical.
- Preferred radicals R 1 are selected from decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl radicals and mixtures thereof, the representatives having an even number of C Atoms are preferred.
- Particularly preferred radicals R 1 are derived from C 12 -C 18 fatty alcohols, for example from coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol or from C 10 -C 20 oxo alcohols.
- AO stands for an ethylene oxide (EO) or propylene oxide (PO) group, preferably for an ethylene oxide group.
- the index n stands for an integer from 1 to 50, preferably from 1 to 20 and in particular from 2 to 10. Very particularly preferably, n stands for the numbers 2, 3, 4, 5, 6, 7 or 8.
- X stands for a monovalent cation or the nth part of an n-valent cation, preferably are the alkali metal ions and among them Na + or K + , with Na + being extremely preferred.
- X + can be selected from H 3 N + CH 2 CH 2 OH, NH 4 + , 1 ⁇ 2 Zn 2+ , 1 ⁇ 2 Mg 2+ , 1 ⁇ 2 Ca 2+ , 1 ⁇ 2 Mn 2+ , and mixtures thereof.
- the degree of ethoxylation indicated represents a statistical mean value, which can be an integer or a fraction for a specific product.
- the degrees of alkoxylation given represent statistical averages, which can be an integer or a fraction for a specific product.
- Preferred alkoxylates / ethoxylates have a narrow homolog distribution (narrow range ethoxylates, NRE).
- the anionic surfactants can be in the form of their sodium, potassium or magnesium or ammonium salts.
- the anionic surfactants are preferably in the form of their sodium salts and / or ammonium salts.
- Amines which can be used for neutralization are preferably choline, triethylamine, monoethanolamine, diethanolamine, triethanolamine, methylethylamine or a mixture thereof, monoethanolamine being preferred.
- textile treatment agents designed as cleaning agents contain additional anionic surfactants in a total amount of 4.0 to 25.0% by weight, in particular 5.0 to 20% by weight.
- the textile treatment agent used according to the invention also contains at least one nonionic surfactant in addition to the glycoside compound (s) used.
- Suitable nonionic surfactants include alkoxylated fatty alcohols, alkoxylated oxo alcohols, alkoxylated fatty acid alkyl esters, fatty acid amides, alkoxylated fatty acid amides, polyhydroxy fatty acid amides, alkylphenol polyglycol ethers, amine oxides, alkyl (poly) glucosides and mixtures thereof.
- R 2 represents a linear or branched, substituted or unsubstituted alkyl radical, preferably a linear, unsubstituted alkyl radical, particularly preferably a fatty alcohol radical.
- Preferred radicals R 2 are selected from decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl radicals and mixtures thereof, the representatives having an even number of C Atoms are preferred.
- radicals R 2 are derived from C 12 -C 18 fatty alcohols, for example from coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol or from C 10 -C 20 oxo alcohols.
- AO stands for an ethylene oxide (EO) or propylene oxide (PO) group, preferably for an ethylene oxide group.
- the index m stands for an integer from 1 to 50, preferably from 1 to 20 and in particular from 2 to 10. Very particularly preferably m stands for the numbers 2, 3, 4, 5, 6, 7 or 8.
- the textile treatment agent used in accordance with the invention can contain further ingredients which further improve the application-related and / or aesthetic properties of the textile treatment agent.
- the textile treatment agent preferably additionally contains one or more substances from the group of enzymes, bleaching agents, complexing agents, builders, electrolytes, non-aqueous solvents, pH regulators, perfumes, perfume carriers, fluorescent agents, dyes, hydrotropes, foam inhibitors, silicone oils, anti-redeposition agents , Graying inhibitors, shrinkage preventers, anti-crease agents, color transfer inhibitors, antimicrobial agents, germicides, fungicides, antioxidants, preservatives, corrosion inhibitors, antistatic agents, bittering agents, ironing aids, phobing and impregnating agents, swelling and anti-slip components, and anti-swelling component, softening agents, softening agents.
- Preferred hydrolytic enzymes include in particular proteases, amylases, in particular ⁇ -amylases, cellulases, lipases, hemicellulases, in particular pectinases, mannanases, ⁇ -glucanases, and mixtures thereof.
- proteases include in particular proteases, amylases, in particular ⁇ -amylases, cellulases, lipases, hemicellulases, in particular pectinases, mannanases, ⁇ -glucanases, and mixtures thereof.
- proteases are particularly preferred and proteases are very particularly preferred.
- these enzymes are of natural origin; Based on the natural molecules, improved variants are available for use in textile treatment agents, in particular detergents, which are accordingly used with preference.
- All substances which destroy or absorb dyes by oxidation, reduction or adsorption and thus discolor materials can serve as bleaching agents. These include bleaches containing hypohalogenite, hydrogen peroxide, perborate, percarbonate, peroxoacetic acid, diperoxoazelaic acid, diperoxododecanedioic acid and oxidative enzyme systems.
- the builders that can be present in the textile treatment agent used according to the invention include, in particular, silicates, aluminum silicates (in particular zeolites), carbonates, salts of organic di- and polycarboxylic acids and mixtures of these substances.
- Organic builders which may be present in the textile treatment agent used according to the invention are, for example, the polycarboxylic acids which can be used in the form of their sodium salts, polycarboxylic acids being understood to mean those carboxylic acids which carry more than one acid function.
- these are citric acid, adipic acid, succinic acid, glutaric acid, malic acid, tartaric acid, maleic acid, fumaric acid, sugar acids, aminocarboxylic acids, and mixtures of these.
- Preferred salts are the salts of polycarboxylic acids such as citric acid, adipic acid, succinic acid, glutaric acid, tartaric acid, sugar acids and mixtures of these.
- Polymeric polycarboxylates are also suitable as builders. These are, for example, the alkali metal salts of polyacrylic acid or polymethacrylic acid, for example those with a relative molecular weight of 600 to 750,000 g / mol.
- the textile treatment agents according to the invention are in liquid form, they preferably contain water as the main solvent. It is preferred that the textile treatment agent contains more than 5% by weight, preferably more than 15% by weight and particularly preferably more than 25% by weight, in each case based on the total amount of textile treatment agent. Particularly preferred liquid textile treatment agents contain - based on their weight - 5 to 90% by weight, preferably 10 to 85% by weight, particularly preferably 25 to 75% by weight and in particular 35 to 65% by weight of water. Alternatively, the textile treatment agents can be water-poor to anhydrous textile treatment agents, the water content in a preferred embodiment being less than 10% by weight and more preferably less than 8% by weight, in each case based on the total liquid textile treatment agent .
- the solvents are preferably selected from ethanol, n-propanol, i-propanol, butanols, glycol, propanediol, butanediol, methylpropanediol, glycerol, diglycol, propyldiglycol, butyldiglycol, hexylene glycol, ethylene glycol methyl ether, ethylene glycol ethyl ether, ethylene glycol propyl ether, ethylene glycol mono-ether, n-butyl butyl Diethylene glycol ethyl ether, propylene glycol methyl ether, propylene glycol ethyl ether, propylene glycol propyl ether, dipropylene glycol monomethyl ether, dipropylene glycol monoethyl ether, methoxytriglycol, ethoxytriglycol, butoxytriglycol, 1-butoxyethoxy-2-propanol, 3-methyl-3-n-
- Softening components which can preferably be used in the textile treatment compositions according to the invention (hereinafter: textile-softening compound) are selected from at least one compound from the group formed from quaternary ammonium compounds, cationic polymers, polysiloxanes, textile-softening clays.
- quaternary ammonium compounds are shown, for example, in the formulas (Q1) and (Q2): where in (Q1) R is an acyclic alkyl radical having 12 to 24 carbon atoms, R 1 is a saturated C 1 -C 4 alkyl or hydroxyalkyl radical, R 2 and R 3 are either the same as R or R 1 or are an aromatic radical .
- X - stands for either a halide, methosulfate, methophosphate or phosphate ion and mixtures of these.
- Examples of cationic compounds of the formula (Q1) are monotalg trimethyl ammonium chloride, monostearyl trimethyl ammonium chloride, didecyl dimethyl ammonium chloride, ditallow dimethyl ammonium chloride or dihexadecyl ammonium chloride.
- R 4 represents an aliphatic alk (en) yl radical having 11 to 21 carbon atoms with 0, 1, 2 or 3 double bonds and / or optionally with substituents
- R 5 stands for H, OH or O (CO) R 7
- R 6 stands independently of R 5 for H, OH or O (CO) R 8
- R 7 and R 8 each independently represent an aliphatic alk (en) yl radical having 11 to 21 carbon atoms with 0, 1, 2 or 3 double bonds.
- m, n and p can each independently have the value 1, 2 or 3.
- X - can be either a halide, methosulfate, methophosphate or phosphate ion, as well as mixtures of these anions.
- R 5 represents the group O (CO) R 7
- R 5 represents the group O (CO) R 7 and R 4 and R 7 are alk (en) yl radicals having 15 to 17 carbon atoms are particularly preferred.
- R 6 is also OH are particularly preferred.
- Ester quats of the formula (Q2) which can preferably be used as plasticizing components are methyl-N- (2-hydroxyethyl) -N, N-di (tallow acyloxyethyl) ammonium methosulfate, methyl-N- (2-hydroxyethyl) -N, N-di ( palmacyloxyethyl) ammonium methosulfate, 1,2-bis- [tallow acyloxy] -3-trimethylammonium propane chloride, N, N-dimethyl-N, N-di (tallow acyloxyethyl) ammonium methosulfate, N, N-dimethyl-N, N-di (tallow acyloxyethyl) -ammonium chloride or methyl-N, N-bis (stearoyloxyethyl) -N- (2-hydroxyethyl) -N, N-di (tallow acyloxyethyl) ammonium
- methylhydroxyalkyldialkoyloxyalkylammonium methosulfates sold by Stepan under the trademark Stepantex® or the products from Cognis known under Dehyquart®, the products from Evonik known under Rewoquat® or the products from Kao known under Tetranyl®.
- plasticizing compounds can be used which have the following groups: RO (CO), N (CO) R or RN (CO), where of these groups, N (CO) R groups are preferred.
- Polydimethylpolysiloxanes are known as efficient textile care compounds.
- Suitable polysiloxanes with the structural units a) and b) are commercially available, for example, under the brand names DC2-8663, DC2-8035, DC2-8203, DC05-7022 or DC2-8566 (all ex Dow Corning).
- the commercially available products Dow Corning® 7224, Dow Corning® 929 Cationic Emulsion or Formasil 410 (GE Silicones) are also suitable.
- Cationic polymers are also suitable textile softening compounds. Some of these also have skin and / or textile care properties.
- Another object of the invention is a method for textile treatment, in which textiles, in particular colored textiles, are brought into contact with a textile with at least one alkyl and / or alkenyl oligoglycoside compound as described in the first object of the invention (in particular as a component of textile treatment agents described above).
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Description
Die Erfindung betrifft das technische Gebiet der Textilbehandlung. Insbesondere wird die Verwendung von Alkyl-/Alkenyl-Oligoglykosidderivaten in Textilbehandlungsmitteln, geeignete Mittel sowie Verfahren zur Behandlung von Textilien beschrieben.The invention relates to the technical field of textile treatment. In particular, the use of alkyl / alkenyl oligoglycoside derivatives in textile treatment agents, suitable agents and processes for treating textiles is described.
Zur Reinigung von Textilien sind diverse tensidhaltige Mittel bekannt, die in einer wässrigen Flotte Beschmutzungen aller Art vom Textil entfernen können. Tenside dienen als waschaktive Substanzen dazu, die Löslichkeit unter anderem von Fett- und Schmutzpartikeln, die an der Wäsche haften, in Wasser zu erhöhen. Die Leistung solcher Mittel an fetthaltigen Anschmutzungen ist allerdings nicht immer optimal, was zur Unzufriedenheit der Verbraucher führt. Es ist ein generelles Bestreben, die Reinigungsleistung von Waschmitteln insbesondere an fetthaltigen Anschmutzungen weiter zu optimieren.Various surfactants are known for cleaning textiles, which can remove all types of soiling from the textile in an aqueous liquor. Surfactants serve as washing-active substances to increase the solubility in water, among other things, of fat and dirt particles that adhere to the laundry. However, the performance of such agents on fatty soiling is not always optimal, which leads to consumer dissatisfaction. There is a general effort to further optimize the cleaning performance of detergents, especially on greasy soiling.
Leider werden durch Textilbehandlungen, insbesondere durch Wäschen, auch wünschenswerte Parameter des Textils verändert. Eine gezielte Färbung bildet eine wichtige und wünschenswerte Eigenschaft gefärbter Textilien. Werden gefärbte Textilien vermehrt einer Textilbehandlung, insbesondere einer Reinigung mit einem Waschmittel, unterworfen, verblasst die Färbung und die Textilien büßen Ihren modischen Reiz ein. Daher fehlte es nicht an Bemühungen die Textilbehandlungsmittel dahingehend zu verbessern, dass (insbesondere neben einer maximalen Reinigungsleistung eines Waschmittels) die Farbverblassung des Textils minimiert wird.Unfortunately, textile treatments, especially washing, also change desirable parameters of the textile. Targeted dyeing is an important and desirable property of dyed textiles. If colored textiles are increasingly subjected to a textile treatment, in particular cleaning with a detergent, the color fades and the textiles lose their fashionable appeal. Therefore, there was no lack of efforts to improve the textile treatment agents so that (in particular in addition to a maximum cleaning performance of a detergent) the color fading of the textile is minimized.
Wenn Farbstoffe aus einer Textilfaser z.B. eines Waschguts herausgelöst werden und in die Flotte übergehen, ist es möglich, dass, z.B. bei Gegenwart verschieden gefärbter Textilien im Waschgut während der Textilbehandlung, nicht nur eine Farbverblassung stattfindet, sondern zusätzlich diese Textilien durch die in die Flotte übergegangenen Farbstoffe verfärbt werden. Die Farbübertragung von Farbstoffen in der Flotte z.B. auf die Textilien des Waschguts muss daher verhindert oder zumindest minimiert werden.If dyes from a textile fiber e.g. of a wash item and transferred to the fleet, it is possible that, e.g. in the presence of differently colored textiles in the laundry during the textile treatment, not only does color fading take place, but these textiles are also discolored by the dyes that have passed into the liquor. The dye transfer of dyes in the fleet e.g. on the textiles in the laundry must therefore be prevented or at least minimized.
Der Fachmann kennt diverse Farbübertragungsinhibitoren, wie beispielsweise Polymere oder Copolymere des N-Vinylimidazols, die insbesondere bei der Formulierung flüssiger Waschmittel zu einer Flockung, Fällung oder Phasentrennung des Waschmittels führen. Es fehlt insbesondere für flüssige Waschmittel, an Farbübertragungsinhibitoren, die mit anionischen Tensiden ausreichend kompatibel sind.The person skilled in the art is familiar with various color transfer inhibitors, such as, for example, polymers or copolymers of N-vinylimidazole, which lead to flocculation, precipitation or phase separation of the detergent, particularly when formulating liquid detergents. In particular for liquid detergents, there is a lack of color transfer inhibitors which are sufficiently compatible with anionic surfactants.
Die japanische Patentveröffentlichung
Aufgabe der vorliegenden Erfindung ist die Bereitstellung von Komponenten für Mittel zur Textilbehandlung, insbesondere zur Behandlung gefärbter Textilien, welche den Farberhalt von Textilien, insbesondere die Entfärbung der Textilien und die die Verfärbung der Textilien im Rahmen einer Textilbehandlung, optimieren bzw. einschränken. Werden diese Komponenten in insbesondere flüssige Zubereitungen eingearbeitet, sollen die Zubereitungen lagerstabil sein. Werden diese Komponenten in Waschmittel eingearbeitet, soll das Waschmittel zumindest eine gleiche oder bessere Reinigungsleistung, insbesondere Primärwaschkraft, besitzen.The object of the present invention is to provide components for agents for textile treatment, in particular for the treatment of dyed textiles, which optimize or restrict the color retention of textiles, in particular the decolorization of the textiles and the discoloration of the textiles as part of a textile treatment. If these components are incorporated into, in particular, liquid preparations, the preparations should be stable in storage. If these components are incorporated into detergent, the detergent should have at least the same or better cleaning performance, in particular primary detergency.
Die Aufgaben werden erfindungsgemäß gelöst durch die Verwendung von Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylaten, -sulfaten, -phosphaten und/oder -isethionaten, die sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableiten,
R-O-(G)p (I)
mit der Bedeutung
- R
- C6-22-Alkyl oder C6-22-Alkenyl,
- G
- Glykosideinheit, die sich von einem Zucker mit 5 oder 6 Kohlenstoffatomen ableitet,
- p
- Zahl von 1 bis 10,
RO- (G) p (I)
with the meaning
- R
- C 6-22 alkyl or C 6-22 alkenyl,
- G
- Glycoside unit derived from a sugar with 5 or 6 carbon atoms,
- p
- Number from 1 to 10,
Es wurde erfindungsgemäß gefunden, dass die Verwendung von Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylaten, -sulfaten, -phosphaten und/oder -isoethionaten in Textilbehandlungsmitteln wie beispielsweise Waschmitteln oder Weichspülern zu einer verbesserten Farbstabilität gefärbter Textilien führt. Insbesondere wird das Verblassen der Textilfarbe und die Verfärbung von Textilien reduziert bis verhindert. Werden besagte Alkyl- und/oder Alkenyloligoglykoside in Waschmitteln verwendet, wird zusätzlich die Reinigungsleistung des Waschmittels, insbesondere die Primärwaschkraft, verbessert.
Bei Einsatz in flüssigen Mitteln, insbesondere flüssigen Waschmitteln, wird verglichen mit herkömmlichen Farbübertragungsinhibitoren, die Lagerstabilität des Mittels erhöht.It has been found according to the invention that the use of alkyl and / or alkenyl oligoglycoside carboxylates, sulfates, phosphates and / or isoethionates in textile treatment agents such as detergents or fabric softeners leads to improved color stability of dyed textiles. In particular, the fading of the textile color and the discoloration of textiles are reduced or prevented. If said alkyl and / or alkenyl oligoglycosides are used in detergents, the cleaning performance of the detergent, in particular the primary detergency, is additionally improved.
When used in liquid compositions, in particular liquid detergents, the storage stability of the composition is increased compared to conventional color transfer inhibitors.
Ein erster Erfindungsgegenstand ist daher die Verwendung von Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylaten, -sulfaten, -phosphaten und/oder -isethionaten, die sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableiten,
R-O-(G)p (I)
mit der Bedeutung
- R
- C6-22-Alkyl oder C6-22-Alkenyl, (bevorzugt C8-18-Alkyl oder C8-18-Alkenyl),
- G
- Glykosideinheit, die sich von einem Zucker mit 5 oder 6 Kohlenstoffatomen ableitet,
- p
- Zahl von 1 bis 10, bevorzugt eine Zahl zwischen 1 und 5.
RO- (G) p (I)
with the meaning
- R
- C 6-22 alkyl or C 6-22 alkenyl, (preferably C 8-18 alkyl or C 8-18 alkenyl),
- G
- Glycoside unit derived from a sugar with 5 or 6 carbon atoms,
- p
- Number from 1 to 10, preferably a number between 1 and 5.
in Textilbehandlungsmitteln, insbesondere Waschmitteln oder Weichspülern, zur Verbesserung der Farbstabilität von damit behandelten gefärbten Textilien, insbesondere zur Reduzierung oder Vermeidung des Entfärbens oder der Verfärbung von damit behandelten gefärbten Textilien .in textile treatment agents, in particular detergents or fabric softeners, to improve the color stability of dyed textiles treated with them, in particular to reduce or avoid discoloration or discoloration of dyed textiles treated with them.
Unter gefärbten Textilien sind insbesondere Textilien zu verstehen, die durch mindestens einen organischen und/oder mindestens einen anorganische Farbstoff eingefärbt wurden, wobei besagte(r) Farbstoff(e) auf das Material des Textils aufgezogen ist/sind und dort für eine gezielte Farbgebung verbleiben soll(en).Dyed textiles are to be understood in particular as textiles which have been dyed by at least one organic and / or at least one inorganic dye, said dye (s) having been applied to the material of the textile and being intended to remain there for targeted coloring (en).
Unter Farbstabilität wird erfindungsgemäß die Beibehaltung einer ursprünglichen Färbung eines gefärbten Textils nach einer oder mehrerer Textilbehandlungen, insbesondere Wäsche und/oder Konditionierung, verstanden. Der Grad der Farbstabilität lässt sich, insbesondere nach mehreren Textilbehandlungen, mir dem bloßem Auge durch Vergleich mit der ursprünglichen Färbung erkennen oder ansonsten geräteanalytisch per farbmetrischer Messung bestimmen.According to the invention, color stability is understood to mean the retention of an original dyeing of a dyed textile after one or more textile treatments, in particular washing and / or conditioning. The degree of color stability, especially after several textile treatments, can be seen with the naked eye by comparison with the original color or otherwise determined by device analysis using colorimetric measurement.
Alle Mengenangaben eines Bestandteils einer Mischung sind, falls nicht anders definiert, Gew.-% bezogen auf das Gesamtgewicht der diesen Bestandteil enthaltenden Mischung.Unless otherwise defined, all amounts of a constituent of a mixture are% by weight based on the total weight of the mixture containing this constituent.
Erfindungsgemäß werden bevorzugt Alkyloligoglykosidcarboxylate, -sulfate, -phosphate und/oderisethionate, besonders bevorzugt Alkyloligoglykosidcarboxylate oder -phosphate, insbesondere Alkylglykosidcarboxylate eingesetzt.According to the invention, alkyl oligoglycoside carboxylates, sulfates, phosphates and / or isethionates are preferably used, particularly preferably alkyl oligoglycoside carboxylates or phosphates, in particular alkyl glycoside carboxylates.
In den Alkyl- und/oder Alkenyl-Oligoglykosiden ist vorzugsweise in mindestens einem der Reste G mindestens eine Hydroxylgruppe durch -O-C1-12-Alkenyl-COOM, -OSO3M, -OP(O)(OM)2 oder -O-CH2-CH2-SO3M , O-CH2-CH2-O-SO3M, jeweils mit M = H, Alkalimetall oder NH4 ersetzt. Dabei wird besonders bevorzugt ein Alkyloligoglykosid-Carboxylat eingesetzt, in dem -O-C1-12-Alkylen-COOM oder -O(CH2-)nCOOM mit M = H, Na oder K und n = 1 bis 3, entsprechend enthalten ist. Besonders bevorzugt ist mindestens eine OH-Gruppe des Rests G gemäß Formel (I) durch eine Gruppe -O-CH2-COONa ersetzt.In the alkyl and / or alkenyl oligoglycosides, at least one hydroxyl group is preferably in at least one of the radicals G by -OC 1-12 -alkenyl-COOM, -OSO 3 M, -OP (O) (OM) 2 or -O- CH 2 -CH 2 -SO 3 M, O-CH 2 -CH 2 -O-SO 3 M, each replaced with M = H, alkali metal or NH 4 . An alkyl oligoglycoside carboxylate is particularly preferably used in which -OC 1-12 alkylene-COOM or -O (CH 2 -) n COOM with M = H, Na or K and n = 1 to 3, is correspondingly contained. At least one OH group of the radical G according to formula (I) is particularly preferably replaced by a group -O-CH 2 -COONa.
Besonders bevorzugt wird ein Alkyloligoglykosidcarboxylat eingesetzt, in dem der Alkylrest ein Laurylrest ist. Speziell bevorzugt ist ein Laurylglucosidcarboxylat, wie es als Plantapon® LGC und Plantapon® LGC sorb von BASF SE erhältlich ist.An alkyl oligoglycoside carboxylate in which the alkyl radical is a lauryl radical is particularly preferably used. A lauryl glucoside carboxylate, such as that available as Plantapon® LGC and Plantapon® LGC sorb from BASF SE, is particularly preferred.
In den Alkylglykosiden der allgemeinen Formel (I) leiten sich die Glykosid-Einheiten G vorzugsweise von Aldosen bzw. Ketosen ab.In the alkyl glycosides of the general formula (I), the glycoside units G are preferably derived from aldoses or ketoses.
Vorzugsweise werden wegen der besseren Reaktionsfähigkeit die reduzierend wirkenden Saccharide, die Aldosen, verwendet. Unter den Aldosen kommt wegen ihrer leichten Zugänglichkeit und technischen Verfügbarkeit insbesondere die Glucose in Betracht. Die als Ausgangsstoffe besonders bevorzugt eingesetzten Alkylglykoside sind daher die Alkylglucoside.Because of the better reactivity, the reducing saccharides, the aldoses, are preferably used. Among the aldoses, glucose is particularly suitable because of its easy accessibility and technical availability. The alkyl glycosides which are particularly preferably used as starting materials are therefore the alkyl glucosides.
Die Indexzahl p in der allgemeinen Formel (I) gibt den Oligomerisierungsgrad, d.h. die Verteilung von Mono- und Oligoglykosiden an und steht für eine Zahl zwischen 1 und 10. Während p in einer gegebenen Verbindung stets ganzzahlig sein muss und hier vor allem die Werte p = 1 bis 6 annehmen kann, ist der Wert p für ein bestimmtes Alkylglykosid eine analytische ermittelte rechnerische Größe, die meistens eine gebrochene Zahl darstellt. Vorzugsweise werden Alkylglykoside mit einem mittleren Oligomerisierungsgrad p von 1,1 bis 3,0 verwendet. Besonders bevorzugt sind solche Alkylglykoside, deren Oligomerisierungsgrad kleiner als 1,5 ist und insbesondere zwischen 1,1, und 1,4 liegt.The index number p in the general formula (I) indicates the degree of oligomerization, i.e. the distribution of mono- and oligoglycosides is present and stands for a number between 1 and 10. While p must always be an integer in a given compound and here can assume the values p = 1 to 6, the value p is for a certain alkyl glycoside an analytically determined arithmetic quantity, which usually represents a fractional number. Alkyl glycosides with an average degree of oligomerization p of 1.1 to 3.0 are preferably used. Those alkyl glycosides whose degree of oligomerization is less than 1.5 and in particular between 1.1 and 1.4 are particularly preferred.
Der Alkylrest R leitet sich von primären Alkoholen mit 6 bis 22, vorzugsweise 12 bis 18 Kohlenstoffatomen ab. Typische Beispiele sind Capronalkohol, Caprylalkohol, Caprinalkohol, Laurylalkohol, Myristylalkohol, Cetylalkohol, Stearylalkohol und Behenylakohol sowie technische Fraktionen, die neben den genannten gesättigten Alkoholen auch Anteile an ungesättigten Alkoholen enthalten können und die auf Basis von natürlichen Fetten und Ölen, beispielsweise Palmöl, Palmkernöl, Kokosöl oder Rindertalg gewonnen werden. Der Einsatz von technischem Kokosalkohol ist hierbei besonders bevorzugt.The alkyl radical R is derived from primary alcohols having 6 to 22, preferably 12 to 18, carbon atoms. Typical examples are capronic alcohol, caprylic alcohol, capric alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol and behenyl alcohol as well as technical fractions which, in addition to the saturated alcohols mentioned, can also contain proportions of unsaturated alcohols and which are based on natural fats and oils, for example palm oil, palm kernel oil, Coconut oil or beef tallow can be obtained. The use of technical coconut alcohol is particularly preferred.
Neben den genannten Fettalkoholen können sich die Alkylglykoside auch von synthetischen primären Alkoholen mit 6 bis 22 Kohlenstoffatomen, insbesondere den sogenannten Oxoalkoholen ableiten, die einen Anteil von 5 bis 40 Gew.-% verzweigter Isomeren aufweisen.In addition to the fatty alcohols mentioned, the alkyl glycosides can also be derived from synthetic primary alcohols having 6 to 22 carbon atoms, in particular the so-called oxo alcohols, which have a proportion of 5 to 40% by weight of branched isomers.
Besonders bevorzugte Alkylreste sind solche mit 8/10, 12/14, 8 bis 16, 12 bis 16 oder 16 bis 18 C-Atomen. Mischungen der Alkylreste ergeben sich bei einer Herstellung ausgehend von natürlichen Fetten und Ölen oder Mineralölen.Particularly preferred alkyl radicals are those with 8/10, 12/14, 8 to 16, 12 to 16 or 16 to 18 carbon atoms. Mixtures of the alkyl residues result from natural fats and oils or mineral oils.
Verfahren zur Herstellung dieser Alkylglykoside sind beispielsweise in den amerikanischen Patentschriften
Für eine weitere Diskussion der Alkyloligo/polyglykoside (APG) kann auf
Die Herstellung der erfindungsgemäß eingesetzten Alkyl- oder Alkenyl-Oligoglykosidcarboxylate, - phosphate, -sulfate oder -isethionate kann nach bekannten Verfahren erfolgen. Die Herstellung der Carboxylate erfolgt beispielsweise durch Umsetzung der Alkyloligoglykoside mit Salzen von Chlorcarbonsäuren in Gegenwart von Basen. Beispielsweise kann mit 2-Chloressigsäure-Natriumsalz in Gegenwart von NaOH umgesetzt werden. Bei der Umsetzung können sowohl die Hydroxylgruppen im Ring wie auch die -CH2-OH-Gruppe umgesetzt werden. Der Umsetzungsgrad ist u.a. abhängig von der Stöchiometrie der Einsatzprodukte. Vorzugsweise werden die Alkyloligoglykoside zumindest an der -CH2-OH-Gruppe umgesetzt, wobei optional ein Mittel eine oder mehreren der am Ring befindlichen Hydroxylgruppen umgesetzt werden können.The alkyl or alkenyl oligoglycoside carboxylates, phosphates, sulfates or isethionates used according to the invention can be prepared by known processes. The carboxylates are prepared, for example, by reacting the alkyl oligoglycosides with salts of chlorocarboxylic acids in the presence of bases. For example, it can be reacted with 2-chloroacetic acid sodium salt in the presence of NaOH. Both the hydroxyl groups in the ring and the —CH 2 —OH group can be reacted in the reaction. The degree of implementation depends, among other things, on the stoichiometry of the input products. The alkyl oligoglycosides are preferably reacted at least on the —CH 2 —OH group, it optionally being possible to react one or more of the hydroxyl groups on the ring.
Weitere Hydroxylgruppen können beispielsweise auch verethert sein.Further hydroxyl groups can also be etherified, for example.
Die Herstellung der Isethionate ist beispielsweise in der
Die Herstellung der Sulfate ist beispielsweise in der
Die Herstellung der Sulfate kann zudem wie in
Weiterhin kann auf die
In der
Die erfindungsgemäß eingesetzten Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylate, -sulfate, - phosphate und/oder -isoethionate werden in Mitteln zur Textilbehandlung insbesondere in Kombination mit mindestens einem zusätzlichen Tensid, verwendet. Dabei handelt es sich bei dem erfindungsgemäß verwendeten Textilbehandlungsmittel bevorzugt um feste Textilwaschmittel, flüssige Textilwaschmittel, flüssige Textilwaschmittel in einer wasserlöslichen Umhüllung, feste Textilweichspüler, flüssige Textilweichspüler. Besonders bevorzugt sind die vorgenannten flüssigen Ausgestaltungen des erfindungsgemäß verwendeten Textilbehandlungsmittels.The alkyl and / or alkenyl oligoglycoside carboxylates, sulfates, phosphates and / or isoethionates used according to the invention are used in agents for textile treatment, in particular in combination with at least one additional surfactant. This is the Textile treatment agents used according to the invention preferably around solid textile detergents, liquid textile detergents, liquid textile detergents in a water-soluble envelope, solid textile fabric softener, liquid fabric softener. The aforementioned liquid configurations of the textile treatment agent used according to the invention are particularly preferred.
Die Textilbehandlungsmittel enthalten mindestens ein Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylat, -sulfat, -phosphat und/oder-isethionat, vorzugsweise in einer Gesamtmenge von 0,1 bis 15 Gew.-%, besonders bevorzugt 0,2 bis 10 Gew.-%. In Textilbehandlungsmitteln zur Konditionierung von Textilien liegen vorzugsweise 0,1 bis 2,0 Gew.-%, besonders bevorzugt 0,2 bis 1,0 Gew.-%, der Glykosidverbindungen vor. Dabei ist es wiederum bevorzugt, wenn besagte Textilbehandlungsmittel zur Konditionierung von Textilien anionische Tenside (d.h. alle anionische Tenside inclusive besagte Oligoglycosid-verbindungen der Formel (I)) in einer Gesamtmenge von 0,1 bis 2,0 Gew.-%, besonders bevorzugt 0,2 bis 1,0 Gew.-%, enthalten.The textile treatment agents contain at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate, preferably in a total amount of 0.1 to 15% by weight, particularly preferably 0.2 to 10% by weight. %. Textile treatment compositions for conditioning textiles preferably contain 0.1 to 2.0% by weight, particularly preferably 0.2 to 1.0% by weight, of the glycoside compounds. It is again preferred if said textile treatment agents for conditioning textiles contain anionic surfactants (ie all anionic surfactants including said oligoglycoside compounds of the formula (I)) in a total amount of 0.1 to 2.0% by weight, particularly preferably 0 , 2 to 1.0% by weight.
In Reinigungsmitteln für Textilien liegen vorzugsweise 1,0 bis 5,0 Gew.-% , besonders bevorzugt 2,0 bis 4,0 Gew.-%, der besagten Glykosidverbindungen gemäß allgemeiner Formel (I) vor. In den reinigenden Textilbehandlungsmitteln können die eingesetzten Glykosidverbindungen gemäß Formel (I) die üblichen anionischen Tenside ganz oder teilweise ersetzen. Damit können die Glykosidverbindungen als alleiniges anionisches Tensid in den Mitteln eingesetzt werden, oder es können Gemische mit üblichen weiteren anionischen Tensiden eingesetzt werden. Diese üblichen anionischen Tenside sind an späterer Stelle näher erläutert. Bevorzugt sind weitere anionische Tenside und die Glykosidverbindungen in einem Gewichtsverhältnis im Bereich von 16 zu 1 bis 1 zu 1, besonders bevorzugt 4 zu 1 bis 2 zu 1, in den erfindungsgemäßen reinigenden Textilbehandlungsmitteln enthalten.In cleaning agents for textiles there are preferably 1.0 to 5.0% by weight, particularly preferably 2.0 to 4.0% by weight, of the glycoside compounds according to general formula (I). In the cleaning textile treatment agents, the glycoside compounds of formula (I) used can completely or partially replace the usual anionic surfactants. The glycoside compounds can thus be used as the sole anionic surfactant in the compositions, or mixtures with customary further anionic surfactants can be used. These common anionic surfactants are explained in more detail later. Further anionic surfactants and the glycoside compounds are preferably present in a weight ratio in the range from 16 to 1 to 1 to 1, particularly preferably 4 to 1 to 2 to 1, in the cleaning textile treatment agents according to the invention.
In den erfindungsgemäß verwendeten Textilbehandlungsmitteln wird insbesondere beim Ersetzen eines Teils oder des ganzen herkömmlichen anionischen Tensids durch die erfindungsgemäß eingesetzte Glykosidverbindung der Formel (I) nach der Textilbehandlung und nachfolgend Untersuchung der Färbung eine erhöhte Farbstabilität festgestellt.In the textile treatment agents used according to the invention, increased color stability is found, in particular when replacing part or all of the conventional anionic surfactant with the glycoside compound of the formula (I) used according to the invention after the textile treatment and subsequent examination of the dyeing.
Die beschriebenen Textilbehandlungsmittel können vorteilhafterweise zur Optimierung der Reinigungsleistung zusätzlich anionische und/oder weitere nichtionische Tenside enthalten.The textile treatment agents described can advantageously additionally contain anionic and / or further nonionic surfactants in order to optimize the cleaning performance.
Geeignete anionische Tenside umfassen, ohne darauf beschränkt zu sein, Alkylbenzolsulfonate, Olefinsulfonate, Alkansulfonate, Fettalkoholsulfate, Fettalkoholethersulfate oder eine Mischung aus zwei oder mehr dieser anionischen Tenside. Von diesen anionischen Tensiden sind Alkylbenzolsulfonate, Fettalkoholethersulfate und Mischungen daraus besonders bevorzugt. Weitere geeignete anionische Tenside sind Seifen, d.h. Salze von Fettsäuren, insbesondere die Na- oder K-Salze von C12-18 Fettsäuren. Seifen können sich insbesondere vorteilhaft auf die Kaltwaschleistung auswirken.Suitable anionic surfactants include, but are not limited to, alkyl benzene sulfonates, olefin sulfonates, alkane sulfonates, fatty alcohol sulfates, fatty alcohol ether sulfates, or a mixture of two or more of these anionic surfactants. Of these anionic surfactants, alkylbenzenesulfonates, fatty alcohol ether sulfates and mixtures thereof are particularly preferred. Other suitable anionic surfactants are soaps, ie salts of fatty acids, especially those Na or K salts of C 12-18 fatty acids. Soaps can have a particularly beneficial effect on the cold washing performance.
Als Tenside vom Sulfonat-Typ kommen dabei vorzugsweise Alkylbenzolsulfonate, Olefinsulfonate, d.h. Gemische aus Alken- und Hydroxyalkansulfonaten sowie Disulfonaten, wie man sie beispielsweise aus C12-18-Monoolefinen mit end- oder innenständiger Doppelbindung durch Sulfonieren mit gasförmigem Schwefeltrioxid und anschließende alkalische oder saure Hydrolyse der Sulfonierungsprodukte erhält, in Betracht. Geeignet sind auch C12-18-Alkansulfonate und die Ester von α-Sulfofettsäuren (Estersulfonate), zum Beispiel die α-sulfonierten Methylester der hydrierten Kokos-, Palmkern- oder Talgfettsäuren.The surfactants of the sulfonate type are preferably alkylbenzenesulfonates, olefin sulfonates, ie mixtures of alkene and hydroxyalkanesulfonates and disulfonates such as are obtained, for example, from C 12-18 monoolefins with terminal or internal double bonds by sulfonation with gaseous sulfur trioxide and subsequent alkaline or acidic Hydrolysis of the sulfonation products is considered. Also suitable are C 12-18 alkanesulfonates and the esters of α-sulfofatty acids (ester sulfonates), for example the α-sulfonated methyl esters of hydrogenated coconut, palm kernel or tallow fatty acids.
Alkylbenzolsulfonate sind vorzugsweise ausgewählt aus linearen oder verzweigten Alkylbenzolsulfonaten der Formel
Als Alk(en)ylsulfate werden die Salze der Schwefelsäurehalbester der C12-C18-Fettalkohole, beispielsweise aus Kokosfettalkohol, Talgfettalkohol, Lauryl-, Myristyl-, Cetyl- oder Stearylalkohol oder der C10-C20-Oxo-Alkohole und diejenigen Halbester sekundärer Alkohole dieser Kettenlängen bevorzugt. Aus waschtechnischem Interesse sind die C12-C16-Alkylsulfate und C12-C15-Alkylsulfate sowie C14-C15-Alkylsulfate bevorzugt. Auch 2,3-Alkylsulfate sind geeignete anionische Tenside. Auch Alkylethersulfate mit der Formel
R1-O-(AO)n-SO3 - X+
sind geeignet. In dieser Formel steht R1 für einen linearen oder verzweigten, substituierten oder unsubstituierten Alkylrest, vorzugsweise für einen linearen, unsubstituierten Alkylrest, besonders bevorzugt für einen Fettalkoholrest. Bevorzugte Reste R1 sind ausgewählt aus Decyl-, Undecyl-, Dodecyl-, Tridecyl-, Tetradecyl, Pentadecyl-, Hexadecyl-, Heptadecyl-, Octadecyl-, Nonadecyl-, Eicosylresten und deren Mischungen, wobei die Vertreter mit gerader Anzahl an C-Atomen bevorzugt sind. Besonders bevorzugte Reste R1 sind abgeleitet von C12-C18-Fettalkoholen, beispielsweise von Kokosfettalkohol, Talgfettalkohol, Lauryl-, Myristyl-, Cetyl- oder Stearylalkohol oder von C10-C20-Oxoalkoholen.The alk (en) yl sulfates are the salts of the sulfuric acid half-esters of the C 12 -C 18 fatty alcohols, for example from coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol or the C 10 -C 20 oxo alcohols and those half-esters secondary alcohols of these chain lengths are preferred. The C 12 -C 16 alkyl sulfates and C 12 -C 15 alkyl sulfates as well as C 14 -C 15 alkyl sulfates are preferred from the point of view of washing technology. 2,3-Alkyl sulfates are also suitable anionic surfactants. Also alkyl ether sulfates with the formula
R 1 -O- (AO) n -SO 3 - X +
are suitable. In this formula, R 1 represents a linear or branched, substituted or unsubstituted alkyl radical, preferably a linear, unsubstituted alkyl radical, particularly preferably a fatty alcohol radical. Preferred radicals R 1 are selected from decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl radicals and mixtures thereof, the representatives having an even number of C Atoms are preferred. Particularly preferred radicals R 1 are derived from C 12 -C 18 fatty alcohols, for example from coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol or from C 10 -C 20 oxo alcohols.
AO steht für eine Ethylenoxid- (EO) oder Propylenoxid- (PO) Gruppierung, vorzugsweise für eine Ethylenoxidgruppierung. Der Index n steht für eine ganze Zahl von 1 bis 50, vorzugsweise von 1 bis 20 und insbesondere von 2 bis 10. Ganz besonders bevorzugt steht n für die Zahlen 2, 3, 4, 5, 6, 7 oder 8. X steht für ein einwertiges Kation oder den n-ten Teil eines n-wertigen Kations, bevorzugt sind dabei die Alkalimetallionen und darunter Na+ oder K+, wobei Na+ äußerst bevorzugt ist. Weitere Kationen X+ können ausgewählt sein aus H3N+CH2CH2OH, NH4 +, ½ Zn2+,½ Mg2+,½ Ca2+,½ Mn2+, und deren Mischungen.AO stands for an ethylene oxide (EO) or propylene oxide (PO) group, preferably for an ethylene oxide group. The index n stands for an integer from 1 to 50, preferably from 1 to 20 and in particular from 2 to 10. Very particularly preferably, n stands for the numbers 2, 3, 4, 5, 6, 7 or 8. X stands for a monovalent cation or the nth part of an n-valent cation, preferably are the alkali metal ions and among them Na + or K + , with Na + being extremely preferred. Further cations X + can be selected from H 3 N + CH 2 CH 2 OH, NH 4 + , ½ Zn 2+ , ½ Mg 2+ , ½ Ca 2+ , ½ Mn 2+ , and mixtures thereof.
Besonders bevorzugt geeignete Textilbehandlungsmittel enthalten ein Alkylethersulfat ausgewählt aus Fettalkoholethersulfaten der Formel
Die anionischen Tenside einschließlich der Fettsäureseifen können in Form ihrer Natrium-, Kalium- oder Magnesium- oder Ammoniumsalze vorliegen. Vorzugsweise liegen die anionischen Tenside in Form ihrer Natriumsalze und/oder Ammoniumsalze vor. Zur Neutralisation einsetzbare Amine sind vorzugsweise Cholin, Triethylamin, Monoethanolamin, Diethanolamin, Triethanolamin, Methylethylamin oder eine Mischung daraus, wobei Monoethanolamin bevorzugt ist.The anionic surfactants, including the fatty acid soaps, can be in the form of their sodium, potassium or magnesium or ammonium salts. The anionic surfactants are preferably in the form of their sodium salts and / or ammonium salts. Amines which can be used for neutralization are preferably choline, triethylamine, monoethanolamine, diethanolamine, triethanolamine, methylethylamine or a mixture thereof, monoethanolamine being preferred.
Es ist erfindungsgemäß bevorzugt, wenn als Reinigungsmittel ausgestaltete Textilbehandlungsmittel zusätzliches Aniontensid in einer Gesamtmenge 4,0 bis 25,0 Gew.-%, insbesondere von 5,0 bis 20 Gew.-%, enthalten.It is preferred according to the invention if textile treatment agents designed as cleaning agents contain additional anionic surfactants in a total amount of 4.0 to 25.0% by weight, in particular 5.0 to 20% by weight.
In verschiedenen Ausführungsformen enthält das erfindungsgemäß verwendete Textilbehandlungsmittel ferner neben der/den eingesetzten Glykosidverbindung(en) mindestens ein nichtionisches Tensid. Geeignete nichtionische Tenside umfassen alkoxylierte Fettalkohole, alkoxylierte Oxo-Alkohole, alkoxylierte Fettsäurealkylester, Fettsäureamide, alkoxylierte Fettsäureamide, Polyhydroxyfettsäureamide, Alkylphenolpolyglycolether, Aminoxide, Alkyl(poly)glucoside und Mischungen daraus.In various embodiments, the textile treatment agent used according to the invention also contains at least one nonionic surfactant in addition to the glycoside compound (s) used. Suitable nonionic surfactants include alkoxylated fatty alcohols, alkoxylated oxo alcohols, alkoxylated fatty acid alkyl esters, fatty acid amides, alkoxylated fatty acid amides, polyhydroxy fatty acid amides, alkylphenol polyglycol ethers, amine oxides, alkyl (poly) glucosides and mixtures thereof.
Bevorzugte Textilbehandlungsmittel enthalten mindestens ein Fettalkoholalkoxylat der Formel
R2-O-(AO)m-H,
in der
- R2
- für einen linearen oder verzweigten, substituierten oder unsubstituierten Alkylrest,
- AO
- für eine Ethylenoxid- (EO) oder Propylenoxid- (PO) Gruppierung,
- m
- für ganze Zahlen von 1 bis 50 stehen.
R 2 -O- (AO) m -H,
in the
- R 2
- for a linear or branched, substituted or unsubstituted alkyl radical,
- AO
- for an ethylene oxide (EO) or propylene oxide (PO) grouping,
- m
- stand for integers from 1 to 50.
In der vorstehend genannten Formel steht R2 für einen linearen oder verzweigten, substituierten oder unsubstituierten Alkylrest, vorzugsweise für einen linearen, unsubstituierten Alkylrest, besonders bevorzugt für einen Fettalkoholrest. Bevorzugte Reste R2 sind ausgewählt aus Decyl-, Undecyl-, Dodecyl-, Tridecyl-, Tetradecyl, Pentadecyl-, Hexadecyl-, Heptadecyl-, Octadecyl-, Nonadecyl-, Eicosylresten und deren Mischungen, wobei die Vertreter mit gerader Anzahl an C-Atomen bevorzugt sind. Besonders bevorzugte Reste R2 sind abgeleitet von C12-C18-Fettalkoholen, beispielsweise von Kokosfettalkohol, Talgfettalkohol, Lauryl-, Myristyl-, Cetyl- oder Stearylalkohol oder von C10-C20-Oxoalkoholen.In the above formula, R 2 represents a linear or branched, substituted or unsubstituted alkyl radical, preferably a linear, unsubstituted alkyl radical, particularly preferably a fatty alcohol radical. Preferred radicals R 2 are selected from decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl radicals and mixtures thereof, the representatives having an even number of C Atoms are preferred. Particularly preferred radicals R 2 are derived from C 12 -C 18 fatty alcohols, for example from coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol or from C 10 -C 20 oxo alcohols.
AO steht für eine Ethylenoxid- (EO) oder Propylenoxid- (PO) Gruppierung, vorzugsweise für eine Ethylenoxidgruppierung. Der Index m steht für eine ganze Zahl von 1 bis 50, vorzugsweise von 1 bis 20 und insbesondere von 2 bis 10. Ganz besonders bevorzugt steht m für die Zahlen 2, 3, 4, 5, 6, 7 oder 8.AO stands for an ethylene oxide (EO) or propylene oxide (PO) group, preferably for an ethylene oxide group. The index m stands for an integer from 1 to 50, preferably from 1 to 20 and in particular from 2 to 10. Very particularly preferably m stands for the numbers 2, 3, 4, 5, 6, 7 or 8.
Zusammenfassend sind besonders bevorzugte Fettalkoholalkoxylate solche der Formel
Es ist erfindungsgemäß bevorzugt, wenn die erfindungsgemäßen Textilbehandlungsmittel, (insbesondere Reinigungsmittel und konditionierende Mittel) nichtionisches Tensid in einer Gesamtmenge 1,0 bis 15,0 Gew.-%, insbesondere 2,0 bis 10,0 Gew.-%, enthalten.It is preferred according to the invention if the textile treatment agents according to the invention (in particular cleaning agents and conditioning agents) contain nonionic surfactant in a total amount of 1.0 to 15.0% by weight, in particular 2.0 to 10.0% by weight.
Es hat sich als besonders vorteilhaft erwiesen, Textilbehandlungsmittel nach einer der Ausführungsformen (A) bis (H) erfindungsgemäß zu verwenden:
- (A) Textilbehandlungsmittel, enthaltend
- mindestens ein Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylat, -sulfat, -phosphat und/oder -isethionat, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
R-O-(G)p (I)
mit der Bedeutung- R
- C6-22-Alkyl oder C6-22-Alkenyl,
- G
- Glykosideinheit, die sich von einem Zucker mit 5 oder 6 Kohlenstoffatomen ableitet,
- p
- Zahl von 1 bis 10,
- mindestens ein zusätzliches anionisches Tensid,
- mindestens ein nichtionisches Tensid.
- mindestens ein Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylat, -sulfat, -phosphat und/oder -isethionat, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
- (B) Textilbehandlungsmittel, enthaltend
- mindestens ein Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylat, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
R-O-(G)p (I)
mit der Bedeutung- R
- C6-22-Alkyl oder C6-22-Alkenyl,
- G
- Glykosideinheit, die sich von einem Zucker mit 5 oder 6 Kohlenstoffatomen ableitet,
- p
- Zahl von 1 bis 10,
- mindestens ein zusätzliches anionisches Tensid,
- mindestens ein nichtionisches Tensid.
- mindestens ein Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylat, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
- (C) Textilbehandlungsmittel, enthaltend
- mindestens ein Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylat, -sulfat, -phosphat und/oder -isethionat, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
R-O-(G)p (I)
mit der Bedeutung- R
- C6-22-Alkyl oder C6-22-Alkenyl,
- G
- Glykosideinheit, die sich von einem Zucker mit 5 oder 6 Kohlenstoffatomen ableitet,
- p
- Zahl von 1 bis 10,
- mindestens ein zusätzliches anionisches Tensid der Formel
R1-O-(CH2CH2O)n-SO3 - X+
worin R1 für einen linearen oder verzweigten, substituierten oder unsubstituierten Alkylrest mit 10 bis 20 Kohlenstoffatomen steht, X für ein einwertiges Kation oder den n-ten Teil eines n-wertigen Kations steht und n = 2, 3, 4, 5, 6, 7 oder 8 ist, - mindestens ein nichtionisches Tensid der Formel
- mindestens ein Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylat, -sulfat, -phosphat und/oder -isethionat, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
- (D) Textilbehandlungsmittel, enthaltend
- mindestens ein Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylat, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
R-O-(G)p (I)
mit der Bedeutung- R
- C6-22-Alkyl oder C6-22-Alkenyl,
- G
- Glykosideinheit, die sich von einem Zucker mit 5 oder 6 Kohlenstoffatomen ableitet,
- p
- Zahl von 1 bis 10,
- mindestens ein zusätzliches anionisches Tensid der Formel
R1-O-(CH2CH2O)n-SO3 - X+
worin R1 für einen linearen oder verzweigten, substituierten oder unsubstituierten Alkylrest mit 10 bis 20 Kohlenstoffatomen steht, X für ein einwertiges Kation oder den n-ten Teil eines n-wertigen Kations steht und n = 2, 3, 4, 5, 6, 7 oder 8 ist, - mindestens ein nichtionisches Tensid der Formel
- mindestens ein Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylat, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
- (E) Textilbehandlungsmittel, enthaltend
- in einer Gesamtmenge von 0,1 bis 15,0 Gew.-% mindestens eines Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylats, -sulfats, -phosphats und/oder-isethionats, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
R-O-(G)p (I)
mit der Bedeutung- R
- C6-22-Alkyl oder C6-22-Alkenyl,
- G
- Glykosideinheit, die sich von einem Zucker mit 5 oder 6 Kohlenstoffatomen ableitet,
- p
- Zahl von 1 bis 10,
- in einer Gesamtmenge von 4,0 bis 20,0 Gew.-% mindestens eines zusätzlichen anionischen Tensids,
- in einer Gesamtmenge von 1,0 bis 15,0 Gew.-% mindestens eines nichtionischen Tensids.
- in einer Gesamtmenge von 0,1 bis 15,0 Gew.-% mindestens eines Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylats, -sulfats, -phosphats und/oder-isethionats, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
- (F) Textilbehandlungsmittel, enthaltend
- in einer Gesamtmenge von 0,1 bis 15,0 Gew.-% mindestens eines Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylats, -sulfats, -phosphats und/oder-isethionats, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
R-O-(G)p (I)
mit der Bedeutung- R
- C6-22-Alkyl oder C6-22-Alkenyl,
- G
- Glykosideinheit, die sich von einem Zucker mit 5 oder 6 Kohlenstoffatomen ableitet,
- p
- Zahl von 1 bis 10,
- in einer Gesamtmenge 4,0 bis 20,0 Gew.-% mindestens eines zusätzlichen anionischen Tensids,
- in einer Gesamtmenge 1,0 bis 15,0 Gew.-% mindestens eines nichtionischen Tensids.
- in einer Gesamtmenge von 0,1 bis 15,0 Gew.-% mindestens eines Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylats, -sulfats, -phosphats und/oder-isethionats, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
- (G) Textilbehandlungsmittel, enthaltend
- in einer Gesamtmenge von 0,1 bis 15,0 Gew.-% mindestens eines Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylats, -sulfats, -phosphats und/oder-isethionats, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
R-O-(G)p (I)
mit der Bedeutung- R
- C6-22-Alkyl oder C6-22-Alkenyl,
- G
- Glykosideinheit, die sich von einem Zucker mit 5 oder 6 Kohlenstoffatomen ableitet,
- p
- Zahl von 1 bis 10,
- in einer Gesamtmenge von 1,0 bis 10,0 Gew.-% mindestens eines zusätzlichen anionischen Tensids der Formel
R1-O-(CH2CH2O)n-SO3 - X+
worin R1 für einen linearen oder verzweigten, substituierten oder unsubstituierten Alkylrest mit 10 bis 20 Kohlenstoffatomen steht, X für ein einwertiges Kation oder den n-ten Teil eines n-wertigen Kations steht und n = 2, 3, 4, 5, 6, 7 oder 8 ist, - in einer Gesamtmenge von 1,0 bis 15,0 Gew.-% mindestens eines nichtionischen Tensids der Formel
- in einer Gesamtmenge von 0,1 bis 15,0 Gew.-% mindestens eines Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylats, -sulfats, -phosphats und/oder-isethionats, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
- (H) Textilbehandlungsmittel, enthaltend
- in einer Gesamtmenge von 0,1 bis 5,0 Gew.-% mindestens eines Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylats, -sulfats, -phosphats und/oder-isethionats, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
R-O-(G)p (I)
mit der Bedeutung- R
- C6-22-Alkyl oder C6-22-Alkenyl,
- G
- Glykosideinheit, die sich von einem Zucker mit 5 oder 6 Kohlenstoffatomen ableitet,
- p
- Zahl von 1 bis 10,
- in einer Gesamtmenge von 1,0 bis 10,0 Gew.-% mindestens eines zusätzlichen anionischen Tensids der Formel
R1-O-(CH2CH2O)n-SO3 - X+
worin R1 für einen linearen oder verzweigten, substituierten oder unsubstituierten Alkylrest mit 10 bis 20 Kohlenstoffatomen steht, X für ein einwertiges Kation oder den n-ten Teil eines n-wertigen Kations steht und n = 2, 3, 4, 5, 6, 7 oder 8 ist, - in einer Gesamtmenge von 1,0 bis 15,0 Gew.-% mindestens eines nichtionischen Tensids der Formel
- in einer Gesamtmenge von 0,1 bis 5,0 Gew.-% mindestens eines Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylats, -sulfats, -phosphats und/oder-isethionats, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
- (A) containing textile treatment agent
- at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate which is derived from alkyl and / or alkenyl oligoglycosides of the general formula (I),
RO- (G) p (I)
with the meaning- R
- C 6-22 alkyl or C 6-22 alkenyl,
- G
- Glycoside unit, which is derived from a sugar with 5 or 6 carbon atoms derives,
- p
- Number from 1 to 10,
- at least one additional anionic surfactant,
- at least one nonionic surfactant.
- at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate which is derived from alkyl and / or alkenyl oligoglycosides of the general formula (I),
- (B) Textile treatment agent containing
- at least one alkyl and / or alkenyl oligoglycoside carboxylate which is derived from alkyl and / or alkenyl oligoglycosides of the general formula (I),
RO- (G) p (I)
with the meaning- R
- C 6-22 alkyl or C 6-22 alkenyl,
- G
- Glycoside unit derived from a sugar with 5 or 6 carbon atoms,
- p
- Number from 1 to 10,
- at least one additional anionic surfactant,
- at least one nonionic surfactant.
- at least one alkyl and / or alkenyl oligoglycoside carboxylate which is derived from alkyl and / or alkenyl oligoglycosides of the general formula (I),
- (C) Textile treatment agent containing
- at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate which is derived from alkyl and / or alkenyl oligoglycosides of the general formula (I),
RO- (G) p (I)
with the meaning- R
- C 6-22 alkyl or C 6-22 alkenyl,
- G
- Glycoside unit derived from a sugar with 5 or 6 carbon atoms,
- p
- Number from 1 to 10,
- at least one additional anionic surfactant of the formula
R 1 -O- (CH 2 CH 2 O) n -SO 3 - X +
in which R 1 represents a linear or branched, substituted or unsubstituted alkyl radical having 10 to 20 carbon atoms, X represents a monovalent cation or the nth part of an n-valent cation and n = 2, 3, 4, 5, 6, Is 7 or 8, - at least one nonionic surfactant of the formula
- at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate which is derived from alkyl and / or alkenyl oligoglycosides of the general formula (I),
- (D) Textile treatment agent containing
- at least one alkyl and / or alkenyl oligoglycoside carboxylate which is derived from alkyl and / or alkenyl oligoglycosides of the general formula (I),
RO- (G) p (I)
with the meaning- R
- C 6-22 alkyl or C 6-22 alkenyl,
- G
- Glycoside unit derived from a sugar with 5 or 6 carbon atoms,
- p
- Number from 1 to 10,
- at least one additional anionic surfactant of the formula
R 1 -O- (CH 2 CH 2 O) n -SO 3 - X +
in which R 1 represents a linear or branched, substituted or unsubstituted alkyl radical having 10 to 20 carbon atoms, X represents a monovalent cation or the nth part of an n-valent cation and n = 2, 3, 4, 5, 6, Is 7 or 8, - at least one nonionic surfactant of the formula
- at least one alkyl and / or alkenyl oligoglycoside carboxylate which is derived from alkyl and / or alkenyl oligoglycosides of the general formula (I),
- (E) Textile treatment agent containing
- in a total amount of 0.1 to 15.0% by weight of at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate, which is derived from alkyl and / or alkenyl oligoglycosides of the general formula ( I) deduces
RO- (G) p (I)
with the meaning- R
- C 6-22 alkyl or C 6-22 alkenyl,
- G
- Glycoside unit derived from a sugar with 5 or 6 carbon atoms,
- p
- Number from 1 to 10,
- in a total amount of 4.0 to 20.0% by weight of at least one additional anionic surfactant,
- in a total amount of 1.0 to 15.0% by weight of at least one nonionic surfactant.
- in a total amount of 0.1 to 15.0% by weight of at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate, which is derived from alkyl and / or alkenyl oligoglycosides of the general formula ( I) deduces
- (F) containing textile treatment agent
- in a total amount of 0.1 to 15.0% by weight of at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate, which is derived from alkyl and / or alkenyl oligoglycosides of the general formula ( I) deduces
RO- (G) p (I)
with the meaning- R
- C 6-22 alkyl or C 6-22 alkenyl,
- G
- Glycoside unit derived from a sugar with 5 or 6 carbon atoms,
- p
- Number from 1 to 10,
- in a total amount of 4.0 to 20.0% by weight of at least one additional anionic surfactant,
- in a total amount of 1.0 to 15.0% by weight of at least one nonionic surfactant.
- in a total amount of 0.1 to 15.0% by weight of at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate, which is derived from alkyl and / or alkenyl oligoglycosides of the general formula ( I) deduces
- (G) Textile treatment agent containing
- in a total amount of 0.1 to 15.0% by weight of at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate, which is derived from alkyl and / or alkenyl oligoglycosides of the general formula ( I) deduces
RO- (G) p (I)
with the meaning- R
- C 6-22 alkyl or C 6-22 alkenyl,
- G
- Glycoside unit derived from a sugar with 5 or 6 carbon atoms,
- p
- Number from 1 to 10,
- in a total amount of 1.0 to 10.0% by weight of at least one additional anionic surfactant of the formula
R 1 -O- (CH 2 CH 2 O) n -SO 3 - X +
in which R 1 represents a linear or branched, substituted or unsubstituted alkyl radical having 10 to 20 carbon atoms, X represents a monovalent cation or the nth part of an n-valent cation and n = 2, 3, 4, 5, 6, Is 7 or 8, - in a total amount of 1.0 to 15.0% by weight of at least one nonionic surfactant of the formula
- in a total amount of 0.1 to 15.0% by weight of at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate, which is derived from alkyl and / or alkenyl oligoglycosides of the general formula ( I) deduces
- (H) Textile treatment agent containing
- in a total amount of 0.1 to 5.0% by weight of at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate, which is derived from alkyl and / or alkenyl oligoglycosides of the general formula ( I) deduces
RO- (G) p (I)
with the meaning- R
- C 6-22 alkyl or C 6-22 alkenyl,
- G
- Glycoside unit derived from a sugar with 5 or 6 carbon atoms,
- p
- Number from 1 to 10,
- in a total amount of 1.0 to 10.0% by weight of at least one additional anionic surfactant of the formula
R 1 -O- (CH 2 CH 2 O) n -SO 3 - X +
in which R 1 represents a linear or branched, substituted or unsubstituted alkyl radical having 10 to 20 carbon atoms, X represents a monovalent cation or the nth part of an n-valent cation and n = 2, 3, 4, 5, 6, Is 7 or 8, - in a total amount of 1.0 to 15.0% by weight of at least one nonionic surfactant of the formula
- in a total amount of 0.1 to 5.0% by weight of at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate, which is derived from alkyl and / or alkenyl oligoglycosides of the general formula ( I) deduces
Die vorgenannten bevorzugten Ausführungsformen der jeweiligen Parameter der Ausführungsformen (A) bis (H) sind selbstredend mutatis mutandis erfindungsgemäß bevorzugt. Ganz besonders bevorzugt sind in den Ausführungsformen (A) bis (H) solche Verbindungen der allgemeinen Formel (I), wobei sich in der allgemeinen Formel (I) die Glykosideinheit G von Aldosen oder Ketosen, insbesondere der Glucose ableitet, p eine Zahl von 1,1 bis 3,0 ist und R ein C12-18-Alkylrest ist. Darüber hinaus ist es zusätzlich bsonders bevorzugt, wenn in mindestens einer der Glycosideinheiten G mindestens eine Hydroxylgruppe durch -O-C1-12-Alkylen-COOM oder -O-(CH2-)nCOOM mit M = H, Na oder K und n =1, 2 oder 3, ersetzt ist.The aforementioned preferred embodiments of the respective parameters of embodiments (A) to (H) are, of course, mutatis mutandis preferred according to the invention. Such compounds of the general formula (I) are very particularly preferred in the embodiments (A) to (H), the glycoside unit G in the general formula (I) being derived from aldoses or ketoses, in particular glucose, p a number of 1 , Is 1 to 3.0 and R is a C 12-18 alkyl group. In addition, it is particularly preferred if at least one of the glycoside units G contains at least one hydroxyl group by -OC 1-12 alkylene-COOM or -O- (CH 2 -) n COOM with M = H, Na or K and n = 1, 2 or 3.
Zusätzlich kann das erfindungsgemäß verwendete Textilbehandlungsmittel generell, sowie bevorzugt deren vorgenannten bevorzugten Ausführungsformen (insbesondere die Ausführungsformen (A) bis (H)), weitere Inhaltsstoffe enthalten, die die anwendungstechnischen und/oder ästhetischen Eigenschaften des Textilbehandlungsmittels weiter verbessern. Im Rahmen der vorliegenden Erfindung enthält das Textilbehandlungsmittel vorzugsweise zusätzlich einen oder mehrere Stoffe aus der Gruppe der Enzyme, Bleichmittel, Komplexbildner, Gerüststoffe, Elektrolyte, nichtwässrigen Lösungsmittel, pH-Stellmittel, Parfüme, Parfümträger, Fluoreszenzmittel, Farbstoffe, Hydrotrope, Schauminhibitoren, Silikonöle, Antiredepositionsmittel, Vergrauungsinhibitoren, Einlaufverhinderer, Knitterschutzmittel, Farbübertragungsinhibitoren, antimikrobiellen Wirkstoffe, Germizide, Fungizide, Antioxidantien, Konservierungsmittel, Korrosionsinhibitoren, Antistatika, Bittermittel, Bügelhilfsmittel, Phobier- und Imprägniermittel, Quell- und Schiebefestmittel, weichmachenden Komponenten sowie UV-Absorber.In addition, the textile treatment agent used in accordance with the invention, and preferably the aforementioned preferred embodiments thereof (in particular embodiments (A) to (H)), can contain further ingredients which further improve the application-related and / or aesthetic properties of the textile treatment agent. In the context of the present invention, the textile treatment agent preferably additionally contains one or more substances from the group of enzymes, bleaching agents, complexing agents, builders, electrolytes, non-aqueous solvents, pH regulators, perfumes, perfume carriers, fluorescent agents, dyes, hydrotropes, foam inhibitors, silicone oils, anti-redeposition agents , Graying inhibitors, shrinkage preventers, anti-crease agents, color transfer inhibitors, antimicrobial agents, germicides, fungicides, antioxidants, preservatives, corrosion inhibitors, antistatic agents, bittering agents, ironing aids, phobing and impregnating agents, swelling and anti-slip components, and anti-swelling component, softening agents, softening agents.
Das erfindungsgemäß verwendete Textilbehandlungsmittel enthält vorzugsweise mindestens ein Enzym. Prinzipiell sind diesbezüglich alle im Stand der Technik für diese Zwecke etablierten Enzyme einsetzbar. Vorzugsweise handelt es sich um eines oder mehrere Enzyme, die in einem Textilbehandlungsmittel eine katalytische Aktivität entfalten können, insbesondere eine Protease, Amylase, Lipase, Cellulase, Hemicellulase, Mannanase, Pektin-spaltendes Enzym, Tannase, Xylanase, Xanthanase, β-Glucosidase, Carrageenase, Perhydrolase, Oxidase, Oxidoreduktase sowie deren Gemische. Bevorzugte hydrolytische Enzyme umfassen insbesondere Proteasen, Amylasen, insbesondere α-Amylasen, Cellulasen, Lipasen, Hemicellulasen, insbesondere Pectinasen, Mannanasen, β-Glucanasen, sowie deren Gemische. Besonders bevorzugt sind Proteasen, Amylasen und/oder Lipasen sowie deren Gemische und ganz besonders bevorzugt sind Proteasen. Diese Enzyme sind im Prinzip natürlichen Ursprungs; ausgehend von den natürlichen Molekülen stehen für den Einsatz in Textilbehandlungsmitteln, insbesondere Waschmitteln, verbesserte Varianten zur Verfügung, die entsprechend bevorzugt eingesetzt werden.The textile treatment agent used according to the invention preferably contains at least one enzyme. In principle, all enzymes established for this purpose in the prior art can be used in this regard. It is preferably one or more enzymes which can develop a catalytic activity in a textile treatment agent, in particular a protease, amylase, lipase, cellulase, hemicellulase, mannanase, pectin-cleaving enzyme, tannase, xylanase, xanthanase, β-glucosidase, carrageenase , Perhydrolase, oxidase, oxidoreductase and mixtures thereof. Preferred hydrolytic enzymes include in particular proteases, amylases, in particular α-amylases, cellulases, lipases, hemicellulases, in particular pectinases, mannanases, β-glucanases, and mixtures thereof. Proteases, amylases and / or lipases and mixtures thereof are particularly preferred and proteases are very particularly preferred. In principle, these enzymes are of natural origin; Based on the natural molecules, improved variants are available for use in textile treatment agents, in particular detergents, which are accordingly used with preference.
Die einzusetzenden Enzyme können ferner zusammen mit Begleitstoffen, etwa aus der Fermentation, oder mit Stabilisatoren konfektioniert sein.The enzymes to be used can also be made up together with accompanying substances, for example from fermentation, or with stabilizers.
Als Bleichmittel können alle Stoffe dienen, die durch Oxidation, Reduktion oder Adsorption Farbstoffe zerstören bzw. aufnehmen und dadurch Materialien entfärben. Dazu gehören unter anderem hypohalogenithaltige Bleichmittel, Wasserstoffperoxid, Perborat, Percarbonat, Peroxoessigsäure, Diperoxoazelainsäure, Diperoxododecandisäure und oxidative Enzymsysteme. Als Gerüststoffe, die in dem erfindungsgemäß verwendeten Textilbehandlungsmittel enthalten sein können, sind insbesondere Silikate, Aluminiumsilikate (insbesondere Zeolithe), Carbonate, Salze organischer Di- und Polycarbonsäuren sowie Mischungen dieser Stoffe zu nennen.All substances which destroy or absorb dyes by oxidation, reduction or adsorption and thus discolor materials can serve as bleaching agents. These include bleaches containing hypohalogenite, hydrogen peroxide, perborate, percarbonate, peroxoacetic acid, diperoxoazelaic acid, diperoxododecanedioic acid and oxidative enzyme systems. The builders that can be present in the textile treatment agent used according to the invention include, in particular, silicates, aluminum silicates (in particular zeolites), carbonates, salts of organic di- and polycarboxylic acids and mixtures of these substances.
Organische Gerüststoffe, welche in dem erfindungsgemäß verwendeten Textilbehandlungsmittel vorhanden sein können, sind beispielsweise die in Form ihrer Natriumsalze einsetzbaren Polycarbonsäuren, wobei unter Polycarbonsäuren solche Carbonsäuren verstanden werden, die mehr als eine Säurefunktion tragen. Beispielsweise sind dies Citronensäure, Adipinsäure, Bernsteinsäure, Glutarsäure, Äpfelsäure, Weinsäure, Maleinsäure, Fumarsäure, Zuckersäuren, Aminocarbonsäuren, sowie Mischungen aus diesen. Bevorzugte Salze sind die Salze der Polycarbonsäuren wie Citronensäure, Adipinsäure, Bernsteinsäure, Glutarsäure, Weinsäure, Zuckersäuren und Mischungen aus diesen.Organic builders which may be present in the textile treatment agent used according to the invention are, for example, the polycarboxylic acids which can be used in the form of their sodium salts, polycarboxylic acids being understood to mean those carboxylic acids which carry more than one acid function. For example, these are citric acid, adipic acid, succinic acid, glutaric acid, malic acid, tartaric acid, maleic acid, fumaric acid, sugar acids, aminocarboxylic acids, and mixtures of these. Preferred salts are the salts of polycarboxylic acids such as citric acid, adipic acid, succinic acid, glutaric acid, tartaric acid, sugar acids and mixtures of these.
Als Gerüststoffe sind weiter polymere Polycarboxylate geeignet. Dies sind beispielsweise die Alkalimetallsalze der Polyacrylsäure oder der Polymethacrylsäure, zum Beispiel solche mit einer relativen Molekülmasse von 600 bis 750.000 g / mol.Polymeric polycarboxylates are also suitable as builders. These are, for example, the alkali metal salts of polyacrylic acid or polymethacrylic acid, for example those with a relative molecular weight of 600 to 750,000 g / mol.
Geeignete Polymere sind insbesondere Polyacrylate, die bevorzugt eine Molekülmasse von 1.000 bis 15.000 g / mol aufweisen. Aufgrund ihrer überlegenen Löslichkeit können aus dieser Gruppe wiederum die kurzkettigen Polyacrylate, die relative Molmassen (Gewichtsmittel) von 1.000 bis 10.000 g / mol, und besonders bevorzugt von 1.000 bis 5.000 g / mol, aufweisen, bevorzugt sein. Geeignet sind weiterhin copolymere Polycarboxylate, insbesondere solche der Acrylsäure mit Methacrylsäure und der Acrylsäure oder Methacrylsäure mit Maleinsäure. Zur Verbesserung der Wasserlöslichkeit können die Polymere auch Allylsulfonsäuren, wie Allyloxybenzolsulfonsäure und Methallylsulfonsäure, als Monomer enthalten.Suitable polymers are, in particular, polyacrylates, which preferably have a molecular weight of 1,000 to 15,000 g / mol. Because of their superior solubility, the short-chain polyacrylates, which have relative molar masses (weight average) from 1,000 to 10,000 g / mol, and particularly preferably from 1,000 to 5,000 g / mol, can in turn be preferred from this group. Also suitable are copolymeric polycarboxylates, in particular those of acrylic acid with methacrylic acid and of acrylic acid or methacrylic acid with maleic acid. To improve water solubility, the polymers can also contain allylsulfonic acids, such as allyloxybenzenesulfonic acid and methallylsulfonic acid, as monomers.
In flüssigen Textilbehandlungsmitteln werden bevorzugt lösliche Gerüststoffe, wie beispielsweise Citronensäure, oder Acrylpolymere mit einer relativen Molmassen (Gewichtsmittel) von 1.000 bis 5.000 g / mol eingesetzt.Soluble builders, such as citric acid, or acrylic polymers with a relative molar mass (weight average) of 1,000 to 5,000 g / mol are preferably used in liquid textile treatment agents.
Liegen die erfindungsgemäßen Textilbehandlungsmittel flüssig vor, so enthalten sie vorzugsweise Wasser als Hauptlösungsmittel. Dabei ist es bevorzugt, dass das Textilbehandlungsmittel mehr als 5 Gew.-%, bevorzugt mehr als 15 Gew.-% und insbesondere bevorzugt mehr als 25 Gew.-%, jeweils bezogen auf die Gesamtmenge an Textilbehandlungsmittel, Wasser enthält. Besonders bevorzugte flüssige Textilbehandlungsmittel enthalten - bezogen auf ihr Gewicht - 5 bis 90 Gew.-%, bevorzugt 10 bis 85 Gew.-%, besonders bevorzugt 25 bis 75 Gew.-% und insbesondere 35 bis 65 Gew.-% Wasser. Alternativ kann es sich bei den Textilbehandlungsmittel um wasserarme bis wasserfreie Textilbehandlungsmittel handeln, wobei der Gehalt an Wasser in einer bevorzugten Ausführungsform weniger als 10 Gew.-% und mehr bevorzugt weniger als 8 Gew.-%, jeweils bezogen auf das gesamte flüssige Textilbehandlungsmittel, beträgt.If the textile treatment agents according to the invention are in liquid form, they preferably contain water as the main solvent. It is preferred that the textile treatment agent contains more than 5% by weight, preferably more than 15% by weight and particularly preferably more than 25% by weight, in each case based on the total amount of textile treatment agent. Particularly preferred liquid textile treatment agents contain - based on their weight - 5 to 90% by weight, preferably 10 to 85% by weight, particularly preferably 25 to 75% by weight and in particular 35 to 65% by weight of water. Alternatively, the textile treatment agents can be water-poor to anhydrous textile treatment agents, the water content in a preferred embodiment being less than 10% by weight and more preferably less than 8% by weight, in each case based on the total liquid textile treatment agent .
Daneben können dem Textilbehandlungsmittel nichtwässrige Lösungsmittel zugesetzt werden. Geeignete nichtwässrige Lösungsmittel umfassen ein- oder mehrwertige Alkohole, Alkanolamine oder Glykolether, sofern sie im angegebenen Konzentrationsbereich mit Wasser mischbar sind. Vorzugsweise werden die Lösungsmittel ausgewählt aus Ethanol, n-Propanol, i-Propanol, Butanolen, Glykol, Propandiol, Butandiol, Methylpropandiol, Glycerin, Diglykol, Propyldiglycol, Butyldiglykol, Hexylenglycol, Ethylenglykolmethylether, Ethylenglykolethylether, Ethylenglykolpropylether, Ethylenglykolmono-n-butylether, Diethylenglykolmethylether, Diethylenglykolethylether, Propylenglykolmethylether, Propylenglykolethylether, Propylenglykolpropylether, Dipropylenglykolmonomethylether, Dipropylenglykolmonoethylether, Methoxytriglykol, Ethoxytriglykol, Butoxytriglykol, 1-Butoxyethoxy-2-propanol, 3-Methyl-3-methoxybutanol, Propylen-glykol-t-butylether, Di-n-octylether sowie Mischungen dieser Lösungsmittel. Es ist allerdings bevorzugt, dass das Textilbehandlungsmittel einen Alkohol, insbesondere Ethanol und/oder Glycerin, in Mengen zwischen 0,5 und 5 Gew.-%, bezogen auf das gesamte Textilbehandlungsmittel enthält.In addition, non-aqueous solvents can be added to the textile treatment agent. Suitable non-aqueous solvents include monohydric or polyhydric alcohols, alkanolamines or glycol ethers, provided that they are miscible with water in the concentration range indicated. The solvents are preferably selected from ethanol, n-propanol, i-propanol, butanols, glycol, propanediol, butanediol, methylpropanediol, glycerol, diglycol, propyldiglycol, butyldiglycol, hexylene glycol, ethylene glycol methyl ether, ethylene glycol ethyl ether, ethylene glycol propyl ether, ethylene glycol mono-ether, n-butyl butyl Diethylene glycol ethyl ether, propylene glycol methyl ether, propylene glycol ethyl ether, propylene glycol propyl ether, dipropylene glycol monomethyl ether, dipropylene glycol monoethyl ether, methoxytriglycol, ethoxytriglycol, butoxytriglycol, 1-butoxyethoxy-2-propanol, 3-methyl-3-n-methoxybutyl ether, mixtures thereof, Solvent. However, it is preferred that the textile treatment agent contains an alcohol, in particular ethanol and / or glycerin, in amounts between 0.5 and 5% by weight, based on the entire textile treatment agent.
Bevorzugt in den erfindungsgemäßen Textilbehandlungsmitteln einsetzbare weichmachende Komponenten (im Folgenden: Textil-weichmachende Verbindung) werden ausgewählt aus mindestens einer Verbindung aus der Gruppe, die gebildet wird aus quaternären Ammoniumverbindungen, kationischen Polymeren, Polysiloxanen, textilweichmachenden Tonen.Softening components which can preferably be used in the textile treatment compositions according to the invention (hereinafter: textile-softening compound) are selected from at least one compound from the group formed from quaternary ammonium compounds, cationic polymers, polysiloxanes, textile-softening clays.
Geeignete Beispiele für quaternäre Ammoniumverbindungen sind beispielsweise in den Formeln (Q1) und (Q2) gezeigt:
Verbindungen der Formel (Q2) sind so genannte Esterquats. Esterquats zeichnen sich durch eine hervorragende biologische Abbaubarkeit aus. In Formel (Q2) steht R4 für einen aliphatischen Alk(en)ylrest mit 11 bis 21 Kohlenstoffatomen mit 0, 1, 2 oder 3 Doppelbindungen und/oder gegebenenfalls mit Substituenten; R5 steht für H, OH oder O(CO)R7, R6 steht unabhängig von R5 für H, OH oder O(CO)R8, wobei R7 und R8 unabhängig voneinander jeweils für einen aliphatischen Alk(en)ylrest mit 11 bis 21 Kohlenstoffatomen mit 0, 1, 2 oder 3 Doppelbindungen steht. m, n und p können jeweils unabhängig voneinander den Wert 1, 2 oder 3 haben. X- kann entweder ein Halogenid-, Methosulfat-, Methophosphat- oder Phosphation sowie Mischungen aus diesen Anionen sein. Bevorzugt sind Verbindungen, bei denen R5 die Gruppe O(CO)R7 darstellt. Besonders bevorzugt sind Verbindungen, bei denen R5 die Gruppe O(CO)R7 darstellt und R4 und R7 Alk(en)ylreste mit 15 bis 17 Kohlenstoffatomen sind. Insbesondere bevorzugt sind Verbindungen, bei denen R6 zudem für OH steht.Compounds of the formula (Q2) are so-called ester quats. Esterquats are characterized by excellent biodegradability. In formula (Q2), R 4 represents an aliphatic alk (en) yl radical having 11 to 21 carbon atoms with 0, 1, 2 or 3 double bonds and / or optionally with substituents; R 5 stands for H, OH or O (CO) R 7 , R 6 stands independently of R 5 for H, OH or O (CO) R 8 , where R 7 and R 8 each independently represent an aliphatic alk (en) yl radical having 11 to 21 carbon atoms with 0, 1, 2 or 3 double bonds. m, n and p can each independently have the value 1, 2 or 3. X - can be either a halide, methosulfate, methophosphate or phosphate ion, as well as mixtures of these anions. Compounds in which R 5 represents the group O (CO) R 7 are preferred. Compounds in which R 5 represents the group O (CO) R 7 and R 4 and R 7 are alk (en) yl radicals having 15 to 17 carbon atoms are particularly preferred. Compounds in which R 6 is also OH are particularly preferred.
Verbindungen der Formel (Q2) werden bevorzugt als textilweichmachenden Verbindungen in den erfindungsgemäßen Textilbehandlungsmitteln eingesetzt. Bevorzugt einsetzbare Esterquats der Formel (Q2) als weichmachende Komponente sind Methyl-N-(2-hydroxyethyl)-N,N-di(talgacyloxyethyl)ammonium-methosulfat, Methyl-N-(2-hydroxyethyl)-N,N-di(palmacyloxyethyl)ammoniummethosulfat, 1,2-Bis-[talgacyloxy]-3-trimethylammoniumpropanchlorid, N,N-Dimethyl-N,N-di(talgacyloxyethyl)ammonium-methosulfat, N,N-Dimethyl-N,N-di(talgacyloxyethyl)-ammoniumchlorid oder Methyl-N,N-bis(stearoyloxyethyl)-N-(2-hydroxyethyl)ammonium-methosulfat.Compounds of the formula (Q2) are preferably used as textile-softening compounds in the textile treatment compositions according to the invention. Ester quats of the formula (Q2) which can preferably be used as plasticizing components are methyl-N- (2-hydroxyethyl) -N, N-di (tallow acyloxyethyl) ammonium methosulfate, methyl-N- (2-hydroxyethyl) -N, N-di ( palmacyloxyethyl) ammonium methosulfate, 1,2-bis- [tallow acyloxy] -3-trimethylammonium propane chloride, N, N-dimethyl-N, N-di (tallow acyloxyethyl) ammonium methosulfate, N, N-dimethyl-N, N-di (tallow acyloxyethyl) -ammonium chloride or methyl-N, N-bis (stearoyloxyethyl) -N- (2-hydroxyethyl) ammonium methosulfate.
Werden quaternierte Verbindungen der Formel (Q2) eingesetzt, die ungesättigte Alkylketten aufweisen, sind die Acylgruppen bevorzugt, deren korrespondierenden Fettsäuren eine Jodzahl zwischen 1 und 100, bevorzugt zwischen 5 und 80, mehr bevorzugt zwischen 10 und 60 und insbesondere zwischen 15 und 45 aufweisen und die ein cis/trans-Isomerenverhältnis (in Gew.-%) von größer als 30 : 70, vorzugsweise größer als 50 : 50 und insbesondere gleich oder größer als 60 : 40 haben. Handelsübliche Beispiele sind die von Stepan unter dem Warenzeichen Stepantex® vertriebenen Methylhydroxyalkyldialkoyloxyalkylammoniummethosulfate oder die unter Dehyquart® bekannten Produkte von Cognis, die unter Rewoquat® bekannten Produkte von Evonik bzw. die unter Tetranyl® bekannten Produkte von Kao.If quaternized compounds of the formula (Q2) are used which have unsaturated alkyl chains, the acyl groups are preferred whose corresponding fatty acids have an iodine number between 1 and 100, preferably between 5 and 80, more preferably between 10 and 60 and in particular between 15 and 45 and which have a cis / trans isomer ratio (in% by weight) of greater than 30:70, preferably greater than 50:50 and in particular equal to or greater than 60:40. Commercial examples are the methylhydroxyalkyldialkoyloxyalkylammonium methosulfates sold by Stepan under the trademark Stepantex® or the products from Cognis known under Dehyquart®, the products from Evonik known under Rewoquat® or the products from Kao known under Tetranyl®.
Anstelle der Estergruppe O(CO)R, wobei R für einen langkettigen Alk(en)ylrest steht, können weichmachende Verbindungen eingesetzt werden, die folgende Gruppen aufweisen: RO(CO), N(CO)R oder RN(CO) weisen, wobei von diesen Gruppen N(CO)R-Gruppen bevorzugt sind.Instead of the ester group O (CO) R, where R stands for a long-chain alk (en) yl radical, plasticizing compounds can be used which have the following groups: RO (CO), N (CO) R or RN (CO), where of these groups, N (CO) R groups are preferred.
Es ist insbesondere bevorzugt, wenn mindestens ein Polysiloxan als Textil-weichmachende Verbindung eingesetzt wird, da diese nicht nur einen weichmachenden Effekt zeigen, sondern auch den Parfümeindruck auf der Wäsche verstärken. Ein bevorzugt einsetzbares Polysiloxan weist zumindest folgende Struktureinheit auf
- R1= unabhängig von einander C1-C30-Alkyl, vorzugsweise C1-C4-Alkyl, insbesondere Methyl oder Ethyl,
- n = 1 bis 5000, vorzugsweise 10 bis 2500, insbesondere 100 bis 1500.
- R 1 = independently of one another C 1 -C 30 alkyl, preferably C 1 -C 4 alkyl, in particular methyl or ethyl,
- n = 1 to 5000, preferably 10 to 2500, in particular 100 to 1500.
Es kann bevorzugt sein, dass das Polysiloxan zusätzlich auch folgende Struktureinheit aufweist:
- R1= C1-C30-Alkyl, vorzugsweise C1-C4-Alkyl, insbesondere Methyl oder Ethyl,
- Y = ggf. substituiertes, lineares oder verzweigtes C1-C20-Alkylen, vorzugsweise -(CH2)m- mit m= 1 bis 16, vorzugsweise 1 bis 8, insbesondere 2 bis 4, im speziellen 3,
- R2, R3 = unabhängig voneinander H oder gegebenenfalls substituiertes, lineares oder verzweigtes C1-C30-Alkyl, vorzugsweise mit Aminogruppen substituiertes C1-C30-Alkyl, besonders bevorzugt - (CH2)b-NH2 mit b = 1 bis 10, äußerst bevorzugt b = 2,
- x = 1 bis 5000, vorzugsweise 10 bis 2500, insbesondere 100 bis 1500.
- R 1 = C 1 -C 30 alkyl, preferably C 1 -C 4 alkyl, especially methyl or ethyl,
- Y = optionally substituted, linear or branched C 1 -C 20 alkylene, preferably - (CH 2 ) m - with m = 1 to 16, preferably 1 to 8, in particular 2 to 4, in particular 3,
- R 2 , R 3 = independently of one another H or optionally substituted, linear or branched C 1 -C 30 -alkyl, preferably C 1 -C 30 -alkyl substituted with amino groups, particularly preferably - (CH 2 ) b -NH 2 with b = 1 to 10, most preferably b = 2,
- x = 1 to 5000, preferably 10 to 2500, in particular 100 to 1500.
Weist das Polysiloxan nur die Struktureinheit a) mit R1 = Methyl auf, handelt es sich um ein Polydimethylsiloxan. Polydimethylpolysiloxane sind als effiziente Textil-pflegende Verbindungen bekannt.If the polysiloxane has only the structural unit a) with R 1 = methyl, it is a polydimethylsiloxane. Polydimethylpolysiloxanes are known as efficient textile care compounds.
Geeignete Polydimethysiloxane umfassen DC-200 (ex Dow Corning), Baysilone® M 50, Baysilone® M 100, Baysilone® M 350, Baysilone® M 500, Baysilone® M 1000, Baysilone® M 1500, Baysilone® M 2000 oder Baysilone® M 5000 (alle ex GE Bayer Silicones).Suitable polydimethysiloxanes include DC-200 (ex Dow Corning), Baysilone® M 50, Baysilone® M 100, Baysilone® M 350, Baysilone® M 500, Baysilone® M 1000, Baysilone® M 1500, Baysilone® M 2000 or Baysilone® M 5000 (all ex GE Bayer Silicones).
Es kann allerdings auch bevorzugt sein, dass das Polysiloxan die Struktureinheiten a) und b) enthält. Ein besonders bevorzugtes Polysiloxan weist die folgende Struktur auf:
(CH3)3Si-[O-Si(CH3)2]n-[O-Si(CH3){(CH2)3-NH-(CH2)2-NH2}]x-OSi(CH3)3
wobei die Summe n + x eine Zahl zwischen 2 und 10.000 ist.However, it can also be preferred that the polysiloxane contains the structural units a) and b). A particularly preferred polysiloxane has the following structure:
(CH 3 ) 3 Si- [O-Si (CH 3 ) 2 ] n - [O-Si (CH 3 ) {(CH 2 ) 3 -NH- (CH 2 ) 2 -NH 2 }] x -OSi ( CH 3 ) 3
where the sum n + x is a number between 2 and 10,000.
Geeignete Polysiloxane mit den Struktureinheiten a) und b) sind beispielsweise kommerziell unter den Markennamen DC2-8663, DC2-8035, DC2-8203, DC05-7022 oder DC2-8566 (alle ex Dow Corning) erhältlich. Ebenfalls geeignet sind beispielsweise die im Handel erhältlichen Produkte Dow Corning® 7224, Dow Corning® 929 Cationic Emulsion oder Formasil 410 (GE Silicones). Weiterhin sind auch kationische Polymere geeignete textilweichmachende Verbindungen. Diese weisen teilweise zusätzlich haut- und/oder textilpflegende Eigenschaften auf. Geeignete kationische Polymere umfassen insbesondere solche, die in "
Ein geeigneter textilweichmachender Ton ist beispielsweise ein Smectit-Ton. Bevorzugte Smectit-Tone sind Beidellit-Tone, Hectorit-Tone, Laponit-Tone, Montmorillonit-Tone, Nontronit-Tone, Saponit-Tone, Sauconit-Tone und Mischungen daraus. Montmorillonit-Tone sind die bevorzugten weichmachenden Tone. Bentonite enthalten hauptsächlich Montmorillonite und können als bevorzugte Quelle für den textilweichmachenden Ton dienen.
- (J) Textilbehandlungsmittel, enthaltend
- mindestens ein Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylat, -sulfat, -phosphat und/oder -isethionat, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
R-O-(G)p (I)
mit der Bedeutung- R
- C6-22-Alkyl oder C6-22-Alkenyl,
- G
- Glykosideinheit, die sich von einem Zucker mit 5 oder 6 Kohlenstoffatomen ableitet,
- p
- Zahl von 1 bis 10,
- mindestens eine quaternäre Ammoniumverbindung ausgewählt aus Formel (Q2)
- R4 steht für einen aliphatischen Alk(en)ylrest mit 11 bis 21 Kohlenstoffatomen mit 0, 1, 2 oder 3 Doppelbindungen und/oder gegebenenfalls mit Substituente;
- R5 steht für H, OH oder O(CO)R7,
- R6 steht unabhängig von R5 für H, OH oder O(CO)R8,
- wobei R7 und R8 unabhängig voneinander jeweils für einen aliphatischen Alk(en)ylrest mit 11 bis 21 Kohlenstoffatomen mit 0, 1, 2 oder 3 Doppelbindungen steht,
- m, n und p haben unabhängig voneinander den Wert 1, 2 oder 3
- X- steht für ein Halogenid-, Methosulfat-, Methophosphat- oder Phosphation sowie Mischungen aus diesen Anionen sein.
- mindestens ein Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylat, -sulfat, -phosphat und/oder -isethionat, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
- (K) Textilbehandlungsmittel, enthaltend
- in einer Gesamtmenge von 0,1 bis 2,0 Gew.-% mindestens eines Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylats, -sulfats, -phosphats und/oder-isethionats, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
R-O-(G)p (I)
mit der Bedeutung- R
- C6-22-Alkyl oder C6-22-Alkenyl,
- G
- Glykosideinheit, die sich von einem Zucker mit 5 oder 6 Kohlenstoffatomen ableitet,
- p
- Zahl von 1 bis 10,
- in einer Gesamtmenge von 0,1 bis 2,0 Gew.-% mindestens einer quaternären Ammoniumverbindung ausgewählt aus Formel (Q2)
- R4 steht für einen aliphatischen Alk(en)ylrest mit 11 bis 21 Kohlenstoffatomen mit 0, 1, 2 oder 3 Doppelbindungen und/oder gegebenenfalls mit Substituente;
- R5 steht für H, OH oder O(CO)R7,
- R6 steht unabhängig von R5 für H, OH oder O(CO)R8,
- wobei R7 und R8 unabhängig voneinander jeweils für einen aliphatischen Alk(en)ylrest mit 11 bis 21 Kohlenstoffatomen mit 0, 1, 2 oder 3 Doppelbindungen steht,
- m, n und p haben unabhängig voneinander den Wert 1, 2 oder 3
- X- steht für ein Halogenid-, Methosulfat-, Methophosphat- oder Phosphation sowie Mischungen aus diesen Anionen sein.
- in einer Gesamtmenge von 0,1 bis 2,0 Gew.-% mindestens eines Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylats, -sulfats, -phosphats und/oder-isethionats, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
- (L) Textilbehandlungsmittel, enthaltend
- in einer Gesamtmenge von 0,1 bis 1,0 Gew.-% mindestens eines Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylats, -sulfats, -phosphats und/oder-isethionats, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
R-O-(G)p (I)
mit der Bedeutung- R
- C6-22-Alkyl oder C6-22-Alkenyl,
- G
- Glykosideinheit, die sich von einem Zucker mit 5 oder 6 Kohlenstoffatomen ableitet,
- p
- Zahl von 1 bis 10,
- in einer Gesamtmenge von 0,1 bis 2,0 Gew.-% mindestens einer quaternären Ammoniumverbindung ausgewählt aus Formel (Q2)
- R4 steht für einen aliphatischen Alk(en)ylrest mit 11 bis 21 Kohlenstoffatomen mit 0, 1, 2 oder 3 Doppelbindungen und/oder gegebenenfalls mit Substituente;
- R5 steht für H, OH oder O(CO)R7,
- R6 steht unabhängig von R5 für H, OH oder O(CO)R8,
- wobei R7 und R8 unabhängig voneinander jeweils für einen aliphatischen Alk(en)ylrest mit 11 bis 21 Kohlenstoffatomen mit 0, 1, 2 oder 3 Doppelbindungen steht,
- m, n und p haben unabhängig voneinander den Wert 1, 2 oder 3
- X- steht für ein Halogenid-, Methosulfat-, Methophosphat- oder Phosphation sowie Mischungen aus diesen Anionen sein.
- in einer Gesamtmenge von 0,1 bis 1,0 Gew.-% mindestens eines Alkyl- und/oder Alkenyl-Oligoglykosidcarboxylats, -sulfats, -phosphats und/oder-isethionats, das sich von Alkyl- und/oder Alkenyloligoglykosiden der allgemeinen Formel (I) ableitet,
- (J) containing textile treatment agent
- at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate which is derived from alkyl and / or alkenyl oligoglycosides of the general formula (I),
RO- (G) p (I)
with the meaning- R
- C 6-22 alkyl or C 6-22 alkenyl,
- G
- Glycoside unit derived from a sugar with 5 or 6 carbon atoms,
- p
- Number from 1 to 10,
- at least one quaternary ammonium compound selected from formula (Q2)
- R 4 represents an aliphatic alk (en) yl radical having 11 to 21 carbon atoms with 0, 1, 2 or 3 double bonds and / or optionally with substituents;
- R 5 stands for H, OH or O (CO) R 7 ,
- R 6 stands independently of R 5 for H, OH or O (CO) R 8 ,
- where R 7 and R 8 each independently represent an aliphatic alk (en) yl radical having 11 to 21 carbon atoms with 0, 1, 2 or 3 double bonds,
- m, n and p are independently 1, 2 or 3
- X - stands for a halide, methosulfate, methophosphate or phosphate ion and mixtures of these anions.
- at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate which is derived from alkyl and / or alkenyl oligoglycosides of the general formula (I),
- (K) Containing textile treatment agents
- in a total amount of 0.1 to 2.0% by weight of at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate, which is derived from alkyl and / or alkenyl oligoglycosides of the general formula ( I) deduces
RO- (G) p (I)
with the meaning- R
- C 6-22 alkyl or C 6-22 alkenyl,
- G
- Glycoside unit derived from a sugar with 5 or 6 carbon atoms,
- p
- Number from 1 to 10,
- in a total amount of 0.1 to 2.0% by weight of at least one quaternary ammonium compound selected from formula (Q2)
- R 4 represents an aliphatic alk (en) yl radical having 11 to 21 carbon atoms with 0, 1, 2 or 3 double bonds and / or optionally with substituents;
- R 5 stands for H, OH or O (CO) R 7 ,
- R 6 stands independently of R 5 for H, OH or O (CO) R 8 ,
- where R 7 and R 8 each independently represent an aliphatic alk (en) yl radical having 11 to 21 carbon atoms with 0, 1, 2 or 3 double bonds,
- m, n and p are independently 1, 2 or 3
- X - stands for a halide, methosulfate, methophosphate or phosphate ion and mixtures of these anions.
- in a total amount of 0.1 to 2.0% by weight of at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate, which is derived from alkyl and / or alkenyl oligoglycosides of the general formula ( I) deduces
- (L) Textile treatment agent containing
- in a total amount of 0.1 to 1.0% by weight of at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate, which is derived from alkyl and / or alkenyl oligoglycosides of the general formula ( I) deduces
RO- (G) p (I)
with the meaning- R
- C 6-22 alkyl or C 6-22 alkenyl,
- G
- Glycoside unit derived from a sugar with 5 or 6 carbon atoms,
- p
- Number from 1 to 10,
- in a total amount of 0.1 to 2.0% by weight of at least one quaternary ammonium compound selected from formula (Q2)
- R 4 represents an aliphatic alk (en) yl radical having 11 to 21 carbon atoms with 0, 1, 2 or 3 double bonds and / or optionally with substituents;
- R 5 stands for H, OH or O (CO) R 7 ,
- R 6 stands independently of R 5 for H, OH or O (CO) R 8 ,
- where R 7 and R 8 each independently represent an aliphatic alk (en) yl radical having 11 to 21 carbon atoms with 0, 1, 2 or 3 double bonds,
- m, n and p are independently 1, 2 or 3
- X - stands for a halide, methosulfate, methophosphate or phosphate ion and mixtures of these anions.
- in a total amount of 0.1 to 1.0% by weight of at least one alkyl and / or alkenyl oligoglycoside carboxylate, sulfate, phosphate and / or isethionate, which is derived from alkyl and / or alkenyl oligoglycosides of the general formula ( I) deduces
Die vorgenannten bevorzugten Ausführungsformen der jeweiligen Parameter der Ausführungsformen (J) bis (L) sind selbstredend mutatis mutandis erfindungsgemäß bevorzugt. Ganz besonders bevorzugt sind in den Ausführungsformen (J) bis (L) solche Verbindungen der allgemeinen Formel (I), wobei sich in der allgemeinen Formel (I) die Glykosideinheit G von Aldosen oder Ketosen, insbesondere der Glucose ableitet, p eine Zahl von 1,1 bis 3,0 ist, R ein C12-18-Alkylrest ist. Darüber hinaus ist es zusätzlich bsonders bevorzugt, wenn in mindestens einer der Glycosideinheiten G mindestens eine Hydroxylgruppe durch -O-C1-12-Alkylen-COOM oder -O-(CH2-)nCOOM mit M = H, Na oder K und n =1, 2 oder 3, ersetzt ist.The aforementioned preferred embodiments of the respective parameters of embodiments (J) to (L) are, of course, mutatis mutandis preferred according to the invention. In the embodiments (J) to (L), such compounds are very particularly preferred general formula (I), wherein in the general formula (I) the glycoside unit G is derived from aldoses or ketoses, in particular glucose, p is a number from 1.1 to 3.0, R is a C 12-18 alkyl radical . In addition, it is particularly preferred if at least one of the glycoside units G contains at least one hydroxyl group by -OC 1-12 alkylene-COOM or -O- (CH 2 -) n COOM with M = H, Na or K and n = 1, 2 or 3.
Ein weiterer Erfindungsgegenstand ist ein Verfahren zur Textilbehandlung, worin Textilien, insbesondere gefärbte Textilien, mit mindestens einer Alkyl- und/oder Alkenyl-Oligoglykosidverbindung wie sie im ersten Erfindungsgegenstand beschrieben wurden (insbesondere als Bestandteil zuvor beschriebener Textilbehandlungsmittel) mit einem Textil in Kontakt gebracht wird.Another object of the invention is a method for textile treatment, in which textiles, in particular colored textiles, are brought into contact with a textile with at least one alkyl and / or alkenyl oligoglycoside compound as described in the first object of the invention (in particular as a component of textile treatment agents described above).
Folgende Flüssigwaschmittelrezeptur wurde durch Vermischen der Komponenten hergestellt:
Es wurden 2 identische Ladungen Buntwäsche mit verschiedenster Farbgebung hergestellt und jede Waschladung mit je einen der Flüssigwaschmittel 20 Mal bei 40°C gewaschen.
Die Farbe der jeweiligen gleichen Wäschestücke aus den Waschladungen wurde miteinander verglichen. Der Farberhalt der mit Flüssigwaschmittel E gewaschenen Waschladung war besser, als der Farberhalt der mit dem Flüssigwaschmittel V gewaschenen Waschladung.Two identical loads of colored laundry with different colors were produced and each washing load was washed with one of the liquid detergents 20 times at 40 ° C.
The color of the same items of laundry from the wash loads was compared. The color retention of the wash load washed with liquid detergent E was better than the color retention of the wash load washed with liquid detergent V.
Claims (7)
- The use of alkyl and/or alkenyl oligoglycoside carboxylates, sulfates, phosphates and/or isethionates which are derived from alkyl and/or alkenyl oligoglycosides of general formula (I),
R-O-(G)p (I)
whereR is C6-22 alkyl or C6-22 alkenyl,G is a glycoside unit derived from a sugar having 5 or 6 carbon atoms,p is a number from 1 to 10,in textile treatment agents, in particular detergents or softeners, to improve the color stability of dyed textiles treated therewith, in particular to reduce or avoid the decolorization and discoloration of dyed textiles treated therewith. - The use according to claim 1, characterized in that, in the alkyl and/or alkenyl oligoglycosides, in at least one of the functional groups G, at least one hydroxyl group is replaced by -O-C1-12 alkenyl-COOM, -OSO3M, -OP(O)(OM)2, -O-CH2-CH2-O-SO3M or -O-CH2-CH2-SO3M where M = H, alkali metal, or NH4.
- The use according to one of the preceding claims, characterized in that, in general formula (I), the glycoside unit G is derived from aldoses or ketoses, in particular glucose, p is a number from 1.1 to 3.0 and R is a C12-18 alkyl functional group.
- The use according to one of the preceding claims, characterized in that an alkyl oligoglycoside carboxylate is used in which, in at least one of the functional groups G, at least one hydroxyl group is replaced by -O-C1-12 alkylene-COOM or -O-(CH2-)n COOM where M = H, Na or K and n = 1, 2 or 3.
- The use according to one of the preceding claims, characterized in that said alkyl and/or alkenyl oligoglycoside compounds are used together with at least one additional anionic surfactant.
- The use according to one of the preceding claims, characterized in that said alkyl and/or alkenyl oligoglycoside compounds are used together with at least one non-ionic surfactant.
- The use according to one of the preceding claims, characterized in that said alkyl and/or alkenyl oligoglycoside compounds are additionally used together with one or more substances from the group of enzymes, bleaching agents, complexing agents, builders, electrolytes, non-aqueous solvents, pH adjusters, perfumes, perfume carriers, fluorescing agents, dyes, hydrotropic substances, suds suppressors, silicone oils, anti-redeposition agents, graying inhibitors, anti-shrink agents, anti-crease agents, dye transfer inhibitors, antimicrobial active ingredients, germicides, fungicides, antioxidants, preservatives, corrosion inhibitors, antistatic agents, bittering agents, ironing aids, repellants and impregnating agents, anti-swelling and anti-slip agents, softening components and UV absorbers.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102013218616.9A DE102013218616A1 (en) | 2013-09-17 | 2013-09-17 | Use of alkyl / alkenyl oligoglycoside derivatives for textile treatment |
PCT/EP2014/069543 WO2015039973A1 (en) | 2013-09-17 | 2014-09-12 | Use of alkyl-/ alkenyl-oligoglycoside derivatives for treating textiles |
Publications (2)
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EP3047011A1 EP3047011A1 (en) | 2016-07-27 |
EP3047011B1 true EP3047011B1 (en) | 2020-04-15 |
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EP14765940.3A Active EP3047011B1 (en) | 2013-09-17 | 2014-09-12 | Use of alkyl-/ alkenyl-oligoglycoside derivatives for treating textiles |
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EP (1) | EP3047011B1 (en) |
DE (1) | DE102013218616A1 (en) |
WO (1) | WO2015039973A1 (en) |
Citations (3)
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WO1988001640A1 (en) * | 1986-09-05 | 1988-03-10 | A.E. Staley Manufacturing Company | Ionic derivatives of alkyl mono and polyglycosides |
WO1998038270A1 (en) * | 1997-02-28 | 1998-09-03 | Henkel Corporation | Dye transfer inhibition system |
JP2007084631A (en) * | 2005-09-20 | 2007-04-05 | Dai Ichi Kogyo Seiyaku Co Ltd | Migration proofing agent |
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US3547828A (en) | 1968-09-03 | 1970-12-15 | Rohm & Haas | Alkyl oligosaccharides and their mixtures with alkyl glucosides and alkanols |
US3839318A (en) | 1970-09-27 | 1974-10-01 | Rohm & Haas | Process for preparation of alkyl glucosides and alkyl oligosaccharides |
US4597770A (en) | 1984-12-24 | 1986-07-01 | The Procter & Gamble Company | Coal-water slurry compositions |
DE3723826A1 (en) | 1987-07-18 | 1989-01-26 | Henkel Kgaa | METHOD FOR PRODUCING ALKYL GLYCOSIDES |
DE4010876A1 (en) | 1990-04-04 | 1991-10-10 | Henkel Kgaa | AQUEOUS SURFACE BLENDS WITH GOOD SKIN TOLERABILITY |
JP3240150B2 (en) * | 1991-04-26 | 2001-12-17 | 花王株式会社 | Detergent composition |
DE4137893A1 (en) | 1991-11-18 | 1993-05-19 | Henkel Kgaa | WAESSER DETERGENSGEMISCHE |
DE4315810A1 (en) | 1993-05-12 | 1994-11-17 | Henkel Kgaa | Aqueous detergent mixtures |
DE19500780A1 (en) | 1995-01-13 | 1996-07-18 | Henkel Kgaa | Cosmetic and pharmaceutical compsns. |
DE19501185A1 (en) | 1995-01-17 | 1996-07-18 | Henkel Kgaa | Synergistic detergent mixts. for hair shampoos or washing up liquids |
DE10027975A1 (en) | 2000-06-06 | 2001-12-13 | Henkel Kgaa | Colorant for keratin fibers, e.g. fur, wool, feathers or especially human hair, contains indole and/or indoline derivative and pyrimidine derivative |
DE10031014A1 (en) | 2000-06-23 | 2002-01-10 | Goldwell Gmbh | Hair Dye |
DE10138094A1 (en) | 2001-08-03 | 2003-02-13 | Henkel Kgaa | Agent for selective coloration of keratin fibers comprises oxidation component containing fatty acid or dicarboxylic acid to give product with stable viscosity |
DE102006004697A1 (en) * | 2006-01-31 | 2007-08-02 | Henkel Kgaa | Detergent or cleaner, useful for colored textile products, comprises surfactants and fatty alkyl dialkylhydroxyethyl ammonium salt as dye transfer inhibitor |
DE102007001115A1 (en) * | 2007-01-04 | 2008-07-10 | Cognis Ip Management Gmbh | Use of aqueous emulsions in foam form for the reload of textiles |
-
2013
- 2013-09-17 DE DE102013218616.9A patent/DE102013218616A1/en not_active Withdrawn
-
2014
- 2014-09-12 EP EP14765940.3A patent/EP3047011B1/en active Active
- 2014-09-12 WO PCT/EP2014/069543 patent/WO2015039973A1/en active Application Filing
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Publication number | Priority date | Publication date | Assignee | Title |
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WO1988001640A1 (en) * | 1986-09-05 | 1988-03-10 | A.E. Staley Manufacturing Company | Ionic derivatives of alkyl mono and polyglycosides |
WO1998038270A1 (en) * | 1997-02-28 | 1998-09-03 | Henkel Corporation | Dye transfer inhibition system |
JP2007084631A (en) * | 2005-09-20 | 2007-04-05 | Dai Ichi Kogyo Seiyaku Co Ltd | Migration proofing agent |
Non-Patent Citations (1)
Title |
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DATABASE WPI Week 200736, Derwent World Patents Index; AN 2007-382651 * |
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DE102013218616A1 (en) | 2015-03-19 |
WO2015039973A1 (en) | 2015-03-26 |
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