CA1330348C - Nonaqueous liquid nonionic laundry detergent composition and method of use - Google Patents
Nonaqueous liquid nonionic laundry detergent composition and method of useInfo
- Publication number
- CA1330348C CA1330348C CA000545512A CA545512A CA1330348C CA 1330348 C CA1330348 C CA 1330348C CA 000545512 A CA000545512 A CA 000545512A CA 545512 A CA545512 A CA 545512A CA 1330348 C CA1330348 C CA 1330348C
- Authority
- CA
- Canada
- Prior art keywords
- percent
- group
- amount
- detergent composition
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000003599 detergent Substances 0.000 title claims abstract description 99
- 239000000203 mixture Substances 0.000 title claims abstract description 80
- 239000007788 liquid Substances 0.000 title claims abstract description 40
- 238000000034 method Methods 0.000 title claims abstract description 8
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 33
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 26
- 150000003839 salts Chemical class 0.000 claims abstract description 25
- 239000004094 surface-active agent Substances 0.000 claims description 33
- 239000003795 chemical substances by application Substances 0.000 claims description 32
- 239000002253 acid Substances 0.000 claims description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 27
- 150000001875 compounds Chemical class 0.000 claims description 22
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 19
- 239000007844 bleaching agent Substances 0.000 claims description 18
- -1 alkylene glycol mono-alkyl ether Chemical class 0.000 claims description 17
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 15
- 239000004744 fabric Substances 0.000 claims description 12
- 102000004190 Enzymes Human genes 0.000 claims description 11
- 108090000790 Enzymes Proteins 0.000 claims description 11
- 239000012190 activator Substances 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 10
- 125000001931 aliphatic group Chemical group 0.000 claims description 9
- 235000019832 sodium triphosphate Nutrition 0.000 claims description 9
- FRPJTGXMTIIFIT-UHFFFAOYSA-N tetraacetylethylenediamine Chemical compound CC(=O)C(N)(C(C)=O)C(N)(C(C)=O)C(C)=O FRPJTGXMTIIFIT-UHFFFAOYSA-N 0.000 claims description 9
- 230000003287 optical effect Effects 0.000 claims description 7
- 239000002304 perfume Substances 0.000 claims description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 6
- 150000003014 phosphoric acid esters Chemical class 0.000 claims description 6
- 238000003860 storage Methods 0.000 claims description 6
- 238000004140 cleaning Methods 0.000 claims description 4
- XSVSPKKXQGNHMD-UHFFFAOYSA-N 5-bromo-3-methyl-1,2-thiazole Chemical compound CC=1C=C(Br)SN=1 XSVSPKKXQGNHMD-UHFFFAOYSA-N 0.000 claims description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 3
- 239000003352 sequestering agent Substances 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 claims description 2
- 125000006538 C11 alkyl 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])* 0.000 claims 3
- 241000237519 Bivalvia Species 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 235000020639 clam Nutrition 0.000 claims 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract description 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 13
- 125000005233 alkylalcohol group Chemical group 0.000 abstract description 8
- 239000000725 suspension Substances 0.000 abstract description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical group CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract description 3
- 239000000047 product Substances 0.000 description 29
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 23
- 150000002191 fatty alcohols Chemical group 0.000 description 19
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 17
- 239000005977 Ethylene Substances 0.000 description 17
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- 150000002500 ions Chemical class 0.000 description 17
- 239000002245 particle Substances 0.000 description 14
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- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 10
- 229920000388 Polyphosphate Polymers 0.000 description 9
- 229940088598 enzyme Drugs 0.000 description 9
- 238000000227 grinding Methods 0.000 description 9
- 239000001205 polyphosphate Substances 0.000 description 9
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
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- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 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 6
- 230000000052 comparative effect Effects 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
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- 229920002125 Sokalan® Polymers 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 5
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- 239000000460 chlorine Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
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- 239000004365 Protease Substances 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
- 230000002378 acidificating effect Effects 0.000 description 4
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- 150000001721 carbon Chemical group 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 4
- 239000004615 ingredient 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
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 3
- 241000047703 Nonion Species 0.000 description 3
- 229920002257 Plurafac® Polymers 0.000 description 3
- 240000001987 Pyrus communis Species 0.000 description 3
- 101100409194 Rattus norvegicus Ppargc1b gene Proteins 0.000 description 3
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
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- 125000004429 atom Chemical group 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
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- 108010003855 mesentericopeptidase Proteins 0.000 description 3
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- ODBPOHVSVJZQRX-UHFFFAOYSA-M sodium;[2-[2-[bis(phosphonomethyl)amino]ethyl-(phosphonomethyl)amino]ethyl-(phosphonomethyl)amino]methyl-hydroxyphosphinate Chemical compound [Na+].OP(=O)(O)CN(CP(O)(O)=O)CCN(CP(O)(=O)O)CCN(CP(O)(O)=O)CP(O)([O-])=O ODBPOHVSVJZQRX-UHFFFAOYSA-M 0.000 description 3
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- YGUMVDWOQQJBGA-VAWYXSNFSA-N 5-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-[(e)-2-[4-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound C=1C=C(\C=C\C=2C(=CC(NC=3N=C(N=C(NC=4C=CC=CC=4)N=3)N3CCOCC3)=CC=2)S(O)(=O)=O)C(S(=O)(=O)O)=CC=1NC(N=C(N=1)N2CCOCC2)=NC=1NC1=CC=CC=C1 YGUMVDWOQQJBGA-VAWYXSNFSA-N 0.000 description 2
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- 238000006482 condensation reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 150000004675 formic acid derivatives Chemical class 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- ACGUYXCXAPNIKK-UHFFFAOYSA-N hexachlorophene Chemical compound OC1=C(Cl)C=C(Cl)C(Cl)=C1CC1=C(O)C(Cl)=CC(Cl)=C1Cl ACGUYXCXAPNIKK-UHFFFAOYSA-N 0.000 description 1
- 229960004068 hexachlorophene Drugs 0.000 description 1
- 125000001145 hydrido group Chemical group *[H] 0.000 description 1
- 229910000378 hydroxylammonium sulfate Inorganic materials 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- VAMFXQBUQXONLZ-UHFFFAOYSA-N icos-1-ene Chemical group CCCCCCCCCCCCCCCCCCC=C VAMFXQBUQXONLZ-UHFFFAOYSA-N 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000010412 laundry washing Methods 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- 229940099990 ogen Drugs 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 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 1
- 229940055729 papain Drugs 0.000 description 1
- 235000019834 papain Nutrition 0.000 description 1
- 229940111202 pepsin Drugs 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- 125000005342 perphosphate group Chemical group 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- HCTVWSOKIJULET-LQDWTQKMSA-M phenoxymethylpenicillin potassium Chemical compound [K+].N([C@H]1[C@H]2SC([C@@H](N2C1=O)C([O-])=O)(C)C)C(=O)COC1=CC=CC=C1 HCTVWSOKIJULET-LQDWTQKMSA-M 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000011012 sanitization Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 235000012976 tarts Nutrition 0.000 description 1
- 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
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- 229960001322 trypsin Drugs 0.000 description 1
- LHMSJZLSCNPWNJ-UHFFFAOYSA-N wyomin Chemical compound OC1C(O)C(O)C(C)OC1OCC1C(O)C(O)C(O)C(OC=2C(=C(O)C=3C(=O)C=C(OC=3C=2)C=2C=C(O)C(O)=CC=2)C2C(C(O)C(O)C(CO)O2)O)O1 LHMSJZLSCNPWNJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/04—Saturated ethers
- C07C43/10—Saturated ethers of polyhydroxy compounds
- C07C43/11—Polyethers containing —O—(C—C—O—)n units with ≤ 2 n≤ 10
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
- C08G65/2606—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups
- C08G65/2609—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups containing aliphatic hydroxyl groups
-
- 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
- C11D1/722—Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US90133986A | 1986-08-28 | 1986-08-28 | |
| US901,339 | 1986-08-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1330348C true CA1330348C (en) | 1994-06-21 |
Family
ID=25413974
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000545512A Expired - Fee Related CA1330348C (en) | 1986-08-28 | 1987-08-27 | Nonaqueous liquid nonionic laundry detergent composition and method of use |
Country Status (19)
| Country | Link |
|---|---|
| JP (1) | JPS6363630A (en)) |
| AU (1) | AU595060B2 (en)) |
| BE (1) | BE1003118A5 (en)) |
| BR (1) | BR8704401A (en)) |
| CA (1) | CA1330348C (en)) |
| CH (1) | CH674358A5 (en)) |
| DE (1) | DE3727793A1 (en)) |
| DK (1) | DK449487A (en)) |
| FR (1) | FR2603277B1 (en)) |
| GB (1) | GB2194536B (en)) |
| IL (1) | IL83635A (en)) |
| IT (1) | IT1211744B (en)) |
| LU (1) | LU86979A1 (en)) |
| MY (1) | MY102879A (en)) |
| NL (1) | NL8702024A (en)) |
| NZ (1) | NZ221508A (en)) |
| PH (1) | PH25005A (en)) |
| SE (1) | SE8703301L (en)) |
| ZA (1) | ZA876157B (en)) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8625974D0 (en) * | 1986-10-30 | 1986-12-03 | Unilever Plc | Non-aqueous liquid detergent |
| CA1339903C (en) * | 1988-08-09 | 1998-06-09 | Eugene Frederick Lutz | Process for the preparation of surfactants having improved physical properties |
| US4919834A (en) * | 1988-09-28 | 1990-04-24 | The Clorox Company | Package for controlling the stability of a liquid nonaqueous detergent |
| US4874537A (en) * | 1988-09-28 | 1989-10-17 | The Clorox Company | Stable liquid nonaqueous detergent compositions |
| GB8906820D0 (en) * | 1989-03-23 | 1989-05-10 | Ici Plc | Novel chemical compounds and their use as low foam surfactants and antifoamingagents |
| SE501132C2 (sv) * | 1992-11-19 | 1994-11-21 | Berol Nobel Ab | Användning av alkoxilat av 2-propylheptanol i rengörande kompositioner |
| DE4311114A1 (de) * | 1993-04-05 | 1994-10-06 | Henkel Kgaa | Detergensgemische |
| DE4314524A1 (de) * | 1993-05-03 | 1994-11-10 | Henkel Ecolab Gmbh & Co Ohg | Mittel zur maschinellen Reinigung und Desinfektion von Textilien |
| DE4404199A1 (de) * | 1994-02-10 | 1995-08-17 | Henkel Kgaa | Reinigungsmittel für harte Oberflächen |
| CN1166856A (zh) * | 1994-09-26 | 1997-12-03 | 普罗格特-甘布尔公司 | 非水含漂白剂的液体洗涤剂组合物 |
| DE19605526A1 (de) | 1996-02-15 | 1997-08-21 | Hoechst Ag | Ammoniumnitrile und deren Verwendung als Bleichaktivatoren |
| DE19719397A1 (de) * | 1997-05-07 | 1998-11-12 | Clariant Gmbh | Bleichaktive Metall-Komplexe |
| DE19728021A1 (de) * | 1997-07-01 | 1999-01-07 | Clariant Gmbh | Metall-Komplexe als Bleichaktivatoren |
| BRPI0720328B1 (pt) * | 2007-01-11 | 2018-06-12 | Dow Global Technologies Inc. | Composição tensoativa e detergente ou limpador. |
| US20240026248A1 (en) * | 2022-07-20 | 2024-01-25 | Ecolab Usa Inc. | Novel nonionic extended surfactants, compositions and methods of use thereof |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2174761A (en) * | 1935-04-13 | 1939-10-03 | Ig Farbenindustrie Ag | Condensation products derived from hydroxy compounds and method of producing them |
| GB1097491A (en) * | 1964-03-09 | 1968-01-03 | Ici Ltd | Improvements in and relating to surface active compounds |
| US3350462A (en) * | 1964-11-24 | 1967-10-31 | Gen Aniline & Film Corp | Preparation of nonionic surface active agents of high wetting power |
| BR7408365D0 (pt) * | 1973-10-12 | 1975-07-29 | Olin Corp | Produto tenso ativo |
| JPS53113805A (en) * | 1977-03-16 | 1978-10-04 | Mitsubishi Petrochem Co Ltd | Nonion surfactant suitable as liquid cleaning agent for clothing |
| US4171455A (en) * | 1978-09-19 | 1979-10-16 | Shiseido Company Ltd. | Polyoxypropylene polyoxyethylene addition ether of higher branched primary saturated alcohol |
| DE2918826A1 (de) * | 1979-05-10 | 1980-11-27 | Basf Ag | Verwendung von alkoxylierten alkoholen als biologisch abbaubare, schaumarme tenside in wasch- und reinigungsmitteln |
| US4308402A (en) * | 1979-11-20 | 1981-12-29 | Shell Oil Company | Process for methyl-capped alkoxylates |
| EP0034194B1 (de) * | 1980-02-18 | 1983-07-13 | Henkel Kommanditgesellschaft auf Aktien | Verfahren zur Herstellung eines schüttfähigen, nichtionische Tenside enthaltenden Wasch- und Reinigungsmittelgranulates |
| GB2145726A (en) * | 1983-08-26 | 1985-04-03 | Diversey Corp | Surface active agents |
| US4753750A (en) * | 1984-12-31 | 1988-06-28 | Delaware | Liquid laundry detergent composition and method of use |
-
1987
- 1987-08-19 MY MYPI87001374A patent/MY102879A/en unknown
- 1987-08-19 ZA ZA876157A patent/ZA876157B/xx unknown
- 1987-08-19 NZ NZ221508A patent/NZ221508A/xx unknown
- 1987-08-20 DE DE19873727793 patent/DE3727793A1/de not_active Withdrawn
- 1987-08-24 AU AU77359/87A patent/AU595060B2/en not_active Ceased
- 1987-08-25 IL IL83635A patent/IL83635A/xx not_active IP Right Cessation
- 1987-08-25 FR FR878711913A patent/FR2603277B1/fr not_active Expired - Fee Related
- 1987-08-25 CH CH3266/87A patent/CH674358A5/de not_active IP Right Cessation
- 1987-08-26 SE SE8703301A patent/SE8703301L/ not_active Application Discontinuation
- 1987-08-27 BR BR8704401A patent/BR8704401A/pt not_active Application Discontinuation
- 1987-08-27 DK DK449487A patent/DK449487A/da not_active Application Discontinuation
- 1987-08-27 CA CA000545512A patent/CA1330348C/en not_active Expired - Fee Related
- 1987-08-27 PH PH35743A patent/PH25005A/en unknown
- 1987-08-27 IT IT8748333A patent/IT1211744B/it active
- 1987-08-28 JP JP62214962A patent/JPS6363630A/ja active Pending
- 1987-08-28 NL NL8702024A patent/NL8702024A/nl not_active Application Discontinuation
- 1987-08-28 BE BE8700959A patent/BE1003118A5/fr not_active IP Right Cessation
- 1987-08-28 LU LU86979A patent/LU86979A1/fr unknown
- 1987-08-28 GB GB8720426A patent/GB2194536B/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| LU86979A1 (fr) | 1988-03-02 |
| IL83635A (en) | 1991-06-30 |
| IL83635A0 (en) | 1988-01-31 |
| ZA876157B (en) | 1989-04-26 |
| BR8704401A (pt) | 1988-04-19 |
| GB8720426D0 (en) | 1987-10-07 |
| JPS6363630A (ja) | 1988-03-22 |
| IT1211744B (it) | 1989-11-03 |
| SE8703301L (sv) | 1988-03-01 |
| FR2603277A1 (fr) | 1988-03-04 |
| AU595060B2 (en) | 1990-03-22 |
| DK449487A (da) | 1988-02-29 |
| SE8703301D0 (sv) | 1987-08-26 |
| NZ221508A (en) | 1989-09-27 |
| AU7735987A (en) | 1988-03-03 |
| CH674358A5 (en)) | 1990-05-31 |
| GB2194536B (en) | 1991-05-22 |
| GB2194536A (en) | 1988-03-09 |
| DE3727793A1 (de) | 1988-03-10 |
| FR2603277B1 (fr) | 1993-08-13 |
| BE1003118A5 (fr) | 1991-12-03 |
| PH25005A (en) | 1991-01-28 |
| DK449487D0 (da) | 1987-08-27 |
| MY102879A (en) | 1993-03-31 |
| NL8702024A (nl) | 1988-03-16 |
| IT8748333A0 (it) | 1987-08-27 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKLA | Lapsed |