ZA200501216B - Gel laundry detergent and/or pre-treater composition - Google Patents

Gel laundry detergent and/or pre-treater composition Download PDF

Info

Publication number: ZA200501216B
Authority: ZA; South Africa
Prior art keywords: composition; surfactant; fatty acid; weight; acid
Prior art date: 2002-09-20

Application number

ZA200501216A

Other languages

English (en)

Inventor

Hsu Feng-Lung Gordon

Zhu Yun-Peng

Vogel Ronald Frederick

Boudou Agnes

Ebert Charles

Hosseini-Nejad Mohammad

Original Assignee

Unilever Plc

Priority date (The priority date 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 date listed.)

2002-09-20

Filing date

2003-08-13

Publication date

2006-11-29

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=31992809&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ZA200501216(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2003-08-13 Application filed by Unilever Plc filed Critical Unilever Plc

2006-11-29 Publication of ZA200501216B publication Critical patent/ZA200501216B/en

Links

239000000203 mixture Substances 0.000 title claims description 110
239000003599 detergent Substances 0.000 title claims description 22
235000014113 dietary fatty acids Nutrition 0.000 claims description 64
239000000194 fatty acid Substances 0.000 claims description 64
229930195729 fatty acid Natural products 0.000 claims description 64
150000004665 fatty acids Chemical class 0.000 claims description 62
239000004094 surface-active agent Substances 0.000 claims description 58
239000004615 ingredient Substances 0.000 claims description 20
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
239000003945 anionic surfactant Substances 0.000 claims description 17
125000000129 anionic group Chemical group 0.000 claims description 14
239000002736 nonionic surfactant Substances 0.000 claims description 14
239000003752 hydrotrope Substances 0.000 claims description 11
239000003093 cationic surfactant Substances 0.000 claims description 10
QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 claims description 10
239000003963 antioxidant agent Substances 0.000 claims description 9
230000003078 antioxidant effect Effects 0.000 claims description 8
229920000642 polymer Polymers 0.000 claims description 7
239000002280 amphoteric surfactant Substances 0.000 claims description 4
125000002091 cationic group Chemical group 0.000 claims description 4
239000000344 soap Substances 0.000 claims description 4
102000004190 Enzymes Human genes 0.000 claims description 3
108090000790 Enzymes Proteins 0.000 claims description 3
239000002689 soil Substances 0.000 claims description 3
239000006172 buffering agent Substances 0.000 claims description 2
239000007850 fluorescent dye Substances 0.000 claims description 2
235000021122 unsaturated fatty acids Nutrition 0.000 claims description 2
150000004670 unsaturated fatty acids Chemical class 0.000 claims description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 51
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 33
239000000499 gel Substances 0.000 description 33
-1 alkali metal salts Chemical class 0.000 description 24
125000000217 alkyl group Chemical group 0.000 description 24
239000011734 sodium Substances 0.000 description 22
229910052708 sodium Inorganic materials 0.000 description 19
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 17
125000004432 carbon atom Chemical group C* 0.000 description 15
239000002253 acid Substances 0.000 description 13
150000003839 salts Chemical class 0.000 description 13
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 12
239000007788 liquid Substances 0.000 description 12
229910052700 potassium Inorganic materials 0.000 description 11
239000011591 potassium Substances 0.000 description 11
239000000047 product Substances 0.000 description 11
150000001875 compounds Chemical class 0.000 description 10
150000002191 fatty alcohols Chemical class 0.000 description 10
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 9
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 9
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 9
150000008051 alkyl sulfates Chemical class 0.000 description 9
238000002156 mixing Methods 0.000 description 9
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 9
239000000600 sorbitol Substances 0.000 description 9
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 8
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 8
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 8
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
239000005642 Oleic acid Substances 0.000 description 8
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 8
235000006708 antioxidants Nutrition 0.000 description 8
239000003795 chemical substances by application Substances 0.000 description 8
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 8
238000000034 method Methods 0.000 description 8
241000283652 Sisko Species 0.000 description 7
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical class [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 7
150000004996 alkyl benzenes Chemical class 0.000 description 7
239000003792 electrolyte Substances 0.000 description 7
239000000463 material Substances 0.000 description 7
229910052783 alkali metal Inorganic materials 0.000 description 6
150000008052 alkyl sulfonates Chemical class 0.000 description 6
239000002585 base Substances 0.000 description 6
239000012071 phase Substances 0.000 description 6
150000003467 sulfuric acid derivatives Chemical class 0.000 description 6
239000004322 Butylated hydroxytoluene Substances 0.000 description 5
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 5
244000060011 Cocos nucifera Species 0.000 description 5
235000013162 Cocos nucifera Nutrition 0.000 description 5
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical class CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 5
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 5
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 5
229910000323 aluminium silicate Inorganic materials 0.000 description 5
229910021538 borax Inorganic materials 0.000 description 5
235000010354 butylated hydroxytoluene Nutrition 0.000 description 5
229940095259 butylated hydroxytoluene Drugs 0.000 description 5
239000000975 dye Substances 0.000 description 5
238000006386 neutralization reaction Methods 0.000 description 5
239000004328 sodium tetraborate Substances 0.000 description 5
235000010339 sodium tetraborate Nutrition 0.000 description 5
QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 5
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 5
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
238000013019 agitation Methods 0.000 description 4
125000001931 aliphatic group Chemical group 0.000 description 4
150000001340 alkali metals Chemical class 0.000 description 4
125000003545 alkoxy group Chemical group 0.000 description 4
230000008901 benefit Effects 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
230000008859 change Effects 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
238000005342 ion exchange Methods 0.000 description 4
229910003002 lithium salt Inorganic materials 0.000 description 4
159000000002 lithium salts Chemical class 0.000 description 4
239000000243 solution Substances 0.000 description 4
PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 4
235000021286 stilbenes Nutrition 0.000 description 4
238000002834 transmittance Methods 0.000 description 4
GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 3
OGTPNDHOHCFDTK-UHFFFAOYSA-N 1,2,3-triphosphonopropan-2-ylphosphonic acid Chemical compound OP(O)(=O)CC(P(O)(O)=O)(P(O)(O)=O)CP(O)(O)=O OGTPNDHOHCFDTK-UHFFFAOYSA-N 0.000 description 3
QJRVOJKLQNSNDB-UHFFFAOYSA-N 4-dodecan-3-ylbenzenesulfonic acid Chemical compound CCCCCCCCCC(CC)C1=CC=C(S(O)(=O)=O)C=C1 QJRVOJKLQNSNDB-UHFFFAOYSA-N 0.000 description 3
RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 3
239000004952 Polyamide Substances 0.000 description 3
239000004721 Polyphenylene oxide Substances 0.000 description 3
BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 3
UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical class OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
239000003086 colorant Substances 0.000 description 3
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 3
229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
239000002304 perfume Substances 0.000 description 3
229920002647 polyamide Polymers 0.000 description 3
229920005646 polycarboxylate Polymers 0.000 description 3
229920000570 polyether Polymers 0.000 description 3
159000000000 sodium salts Chemical class 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
238000012360 testing method Methods 0.000 description 3
238000004383 yellowing Methods 0.000 description 3
239000002888 zwitterionic surfactant Substances 0.000 description 3
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
239000004255 Butylated hydroxyanisole Substances 0.000 description 2
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
229920002257 Plurafac® Polymers 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
239000004743 Polypropylene Substances 0.000 description 2
ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 2
RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
239000006096 absorbing agent Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
239000002518 antifoaming agent Substances 0.000 description 2
230000009286 beneficial effect Effects 0.000 description 2
SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 2
150000001642 boronic acid derivatives Chemical class 0.000 description 2
235000019282 butylated hydroxyanisole Nutrition 0.000 description 2
CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 description 2
229940043253 butylated hydroxyanisole Drugs 0.000 description 2
239000004202 carbamide Substances 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
150000004649 carbonic acid derivatives Chemical class 0.000 description 2
150000007942 carboxylates Chemical class 0.000 description 2
238000004140 cleaning Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
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LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
235000011187 glycerol Nutrition 0.000 description 2
125000000623 heterocyclic group Chemical group 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
239000004973 liquid crystal related substance Substances 0.000 description 2
238000005259 measurement Methods 0.000 description 2
YDSWCNNOKPMOTP-UHFFFAOYSA-N mellitic acid Chemical class OC(=O)C1=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C(C(O)=O)=C1C(O)=O YDSWCNNOKPMOTP-UHFFFAOYSA-N 0.000 description 2
230000003472 neutralizing effect Effects 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
239000012188 paraffin wax Substances 0.000 description 2
239000002245 particle Substances 0.000 description 2
235000002949 phytic acid Nutrition 0.000 description 2
239000000049 pigment Substances 0.000 description 2
229920000573 polyethylene Polymers 0.000 description 2
229920000139 polyethylene terephthalate Polymers 0.000 description 2
239000005020 polyethylene terephthalate Substances 0.000 description 2
229920005862 polyol Polymers 0.000 description 2
150000003077 polyols Chemical class 0.000 description 2
229920001155 polypropylene Polymers 0.000 description 2
239000002243 precursor Substances 0.000 description 2
238000012545 processing Methods 0.000 description 2
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150000004760 silicates Chemical class 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
239000004250 tert-Butylhydroquinone Substances 0.000 description 2
235000019281 tert-butylhydroquinone Nutrition 0.000 description 2
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239000002562 thickening agent Substances 0.000 description 2
150000003852 triazoles Chemical class 0.000 description 2
238000005406 washing Methods 0.000 description 2
CIOXZGOUEYHNBF-UHFFFAOYSA-N (carboxymethoxy)succinic acid Chemical class OC(=O)COC(C(O)=O)CC(O)=O CIOXZGOUEYHNBF-UHFFFAOYSA-N 0.000 description 1
SFRLSTJPMFGBDP-UHFFFAOYSA-N 1,2-diphosphonoethylphosphonic acid Chemical class OP(O)(=O)CC(P(O)(O)=O)P(O)(O)=O SFRLSTJPMFGBDP-UHFFFAOYSA-N 0.000 description 1
YVPHSTVRTGSOSK-UHFFFAOYSA-N 1,3,3-triphosphonopropylphosphonic acid Chemical compound OP(O)(=O)C(P(O)(O)=O)CC(P(O)(O)=O)P(O)(O)=O YVPHSTVRTGSOSK-UHFFFAOYSA-N 0.000 description 1
TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
PQHYOGIRXOKOEJ-UHFFFAOYSA-N 2-(1,2-dicarboxyethylamino)butanedioic acid Chemical class OC(=O)CC(C(O)=O)NC(C(O)=O)CC(O)=O PQHYOGIRXOKOEJ-UHFFFAOYSA-N 0.000 description 1
VIFBEEYZXDDZCT-UHFFFAOYSA-N 2-(2-phenylethenyl)benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1C=CC1=CC=CC=C1 VIFBEEYZXDDZCT-UHFFFAOYSA-N 0.000 description 1
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IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
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ATGAWOHQWWULNK-UHFFFAOYSA-I pentapotassium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical class [K+].[K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O ATGAWOHQWWULNK-UHFFFAOYSA-I 0.000 description 1
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235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
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FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
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125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
DIORMHZUUKOISG-UHFFFAOYSA-N sulfoformic acid Chemical compound OC(=O)S(O)(=O)=O DIORMHZUUKOISG-UHFFFAOYSA-N 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
239000006188 syrup Substances 0.000 description 1
235000020357 syrup Nutrition 0.000 description 1
239000003760 tallow Substances 0.000 description 1
235000015523 tannic acid Nutrition 0.000 description 1
LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
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BDOBMVIEWHZYDL-UHFFFAOYSA-N tetrachlorosalicylanilide Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC=C1 BDOBMVIEWHZYDL-UHFFFAOYSA-N 0.000 description 1
JZBRFIUYUGTUGG-UHFFFAOYSA-J tetrapotassium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical class [K+].[K+].[K+].[K+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O JZBRFIUYUGTUGG-UHFFFAOYSA-J 0.000 description 1
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VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
235000013799 ultramarine blue Nutrition 0.000 description 1
KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical class CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 1
235000019154 vitamin C Nutrition 0.000 description 1
239000011718 vitamin C Substances 0.000 description 1
235000019165 vitamin E Nutrition 0.000 description 1
239000011709 vitamin E Substances 0.000 description 1
229940046009 vitamin E Drugs 0.000 description 1
239000008096 xylene Chemical class 0.000 description 1
229940071104 xylenesulfonate Drugs 0.000 description 1
239000010457 zeolite Substances 0.000 description 1
UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
239000004711 α-olefin Substances 0.000 description 1
GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
- C11D3/2079—Monocarboxylic acids-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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/003—Colloidal solutions, e.g. gels; Thixotropic solutions or pastes

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Emergency Medicine (AREA)
Dispersion Chemistry (AREA)
Detergent Compositions (AREA)

ZA200501216A 2002-09-20 2003-08-13 Gel laundry detergent and/or pre-treater composition ZA200501216B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US10/251,738 US6794348B2 (en)	2002-09-20	2002-09-20	Gel laundry detergent and/or pre-treater composition

Publications (1)

Publication Number	Publication Date
ZA200501216B true ZA200501216B (en)	2006-11-29

Family

ID=31992809

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200501216A ZA200501216B (en)	2002-09-20	2003-08-13	Gel laundry detergent and/or pre-treater composition

Country Status (9)

Country	Link
US (1)	US6794348B2 (de)
EP (1)	EP1539915B1 (de)
AR (1)	AR041301A1 (de)
AT (1)	ATE346907T1 (de)
AU (1)	AU2003255428A1 (de)
BR (1)	BR0314043A (de)
DE (1)	DE60310092T2 (de)
WO (1)	WO2004027010A1 (de)
ZA (1)	ZA200501216B (de)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA2535218C (en) *	2003-09-16	2012-04-03	Unilever Plc	Gel laundry detergent composition
US7018970B2 (en) *	2003-10-28	2006-03-28	Unilever Home And Personal Care Usa Division Of Conopco, Inc.	Process of making fatty alcohol based gel detergent compositions
US20050274399A1 (en) *	2004-06-15	2005-12-15	Heise Karl A	Method of fomulating a cleaning composition in a concentrated form
US20080032909A1 (en) *	2006-05-05	2008-02-07	De Buzzaccarini Francesco	Compact fluid laundry detergent composition
US20080015135A1 (en) *	2006-05-05	2008-01-17	De Buzzaccarini Francesco	Compact fluid laundry detergent composition
US20070270325A1 (en) *	2006-05-05	2007-11-22	De Buzzaccarini Francesco	Gel compositions contained in bottom dispensing containers
DE102009028891A1 (de) *	2009-08-26	2011-03-03	Henkel Ag & Co. Kgaa	Verbesserte Waschleistung durch Radikalfänger
UY33129A (es) *	2009-12-21	2011-01-31	Colgate Palmolive Co	Lavavajillas en pasta
EP2551335A1 (de)	2011-07-25	2013-01-30	The Procter & Gamble Company	Flüssige Waschmittelzusammensetzung mit stabilisiertem Enzym
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2002
- 2002-09-20 US US10/251,738 patent/US6794348B2/en not_active Expired - Lifetime
2003
- 2003-08-13 BR BR0314043-1A patent/BR0314043A/pt not_active IP Right Cessation
- 2003-08-13 EP EP03797236A patent/EP1539915B1/de not_active Revoked
- 2003-08-13 DE DE60310092T patent/DE60310092T2/de not_active Expired - Fee Related
- 2003-08-13 ZA ZA200501216A patent/ZA200501216B/en unknown
- 2003-08-13 WO PCT/EP2003/008952 patent/WO2004027010A1/en not_active Ceased
- 2003-08-13 AU AU2003255428A patent/AU2003255428A1/en not_active Abandoned
- 2003-08-13 AT AT03797236T patent/ATE346907T1/de not_active IP Right Cessation
- 2003-09-18 AR ARP030103387A patent/AR041301A1/es not_active Application Discontinuation

Also Published As

Publication number	Publication date
DE60310092T2 (de)	2007-04-12
AR041301A1 (es)	2005-05-11
EP1539915B1 (de)	2006-11-29
EP1539915A1 (de)	2005-06-15
DE60310092D1 (de)	2007-01-11
US6794348B2 (en)	2004-09-21
AU2003255428A1 (en)	2004-04-08
BR0314043A (pt)	2005-07-19
ATE346907T1 (de)	2006-12-15
WO2004027010A1 (en)	2004-04-01
US20040058838A1 (en)	2004-03-25

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