CH675251A5 - - Google Patents

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Publication number: CH675251A5
Authority: CH; Switzerland
Prior art keywords: composition according; liquid; agent; surfactant; bleach
Prior art date: 1986-09-09

Application number

CH3402/87A

Other languages

German (de)

English (en)

Inventor

Guy Broze

Danielle Bastin

Original Assignee

Colgate Palmolive Co

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.)

1986-09-09

Filing date

1987-09-04

Publication date

1990-09-14

1987-09-04 Application filed by Colgate Palmolive Co filed Critical Colgate Palmolive Co

1990-09-14 Publication of CH675251A5 publication Critical patent/CH675251A5/de

Links

239000000203 mixture Substances 0.000 claims description 114
239000007788 liquid Substances 0.000 claims description 87
239000002736 nonionic surfactant Substances 0.000 claims description 87
239000007844 bleaching agent Substances 0.000 claims description 80
239000003599 detergent Substances 0.000 claims description 65
239000012190 activator Substances 0.000 claims description 43
150000001875 compounds Chemical class 0.000 claims description 39
-1 alkylene glycol monoalkyl ether Chemical class 0.000 claims description 35
239000002245 particle Substances 0.000 claims description 33
150000003839 salts Chemical class 0.000 claims description 31
239000004094 surface-active agent Substances 0.000 claims description 31
239000003795 chemical substances by application Substances 0.000 claims description 30
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 24
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 23
150000002148 esters Chemical class 0.000 claims description 20
239000000725 suspension Substances 0.000 claims description 17
102000004190 Enzymes Human genes 0.000 claims description 16
108090000790 Enzymes Proteins 0.000 claims description 16
235000019832 sodium triphosphate Nutrition 0.000 claims description 16
239000002253 acid Substances 0.000 claims description 14
239000004753 textile Substances 0.000 claims description 14
125000000217 alkyl group Chemical group 0.000 claims description 13
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 12
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 12
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 12
239000002304 perfume Substances 0.000 claims description 11
230000003287 optical effect Effects 0.000 claims description 10
239000003352 sequestering agent Substances 0.000 claims description 10
239000003381 stabilizer Substances 0.000 claims description 10
239000000654 additive Substances 0.000 claims description 9
238000004140 cleaning Methods 0.000 claims description 8
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 7
238000004061 bleaching Methods 0.000 claims description 7
238000001556 precipitation Methods 0.000 claims description 7
UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 claims description 7
239000001205 polyphosphate Substances 0.000 claims description 6
235000011176 polyphosphates Nutrition 0.000 claims description 6
229920000388 Polyphosphate Polymers 0.000 claims description 5
229920001577 copolymer Polymers 0.000 claims description 5
229940028356 diethylene glycol monobutyl ether Drugs 0.000 claims description 5
239000002608 ionic liquid Substances 0.000 claims description 5
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 5
JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 claims description 5
230000003213 activating effect Effects 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
150000002894 organic compounds Chemical class 0.000 claims description 4
159000000000 sodium salts Chemical class 0.000 claims description 4
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 3
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims description 2
101150065749 Churc1 gene Proteins 0.000 claims description 2
102100038239 Protein Churchill Human genes 0.000 claims description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
230000000996 additive effect Effects 0.000 claims 2
MTHSVFCYNBDYFN-UHFFFAOYSA-N anhydrous diethylene glycol Natural products OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims 2
239000004215 Carbon black (E152) Substances 0.000 claims 1
239000002671 adjuvant Substances 0.000 claims 1
229930195733 hydrocarbon Natural products 0.000 claims 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 31
239000000047 product Substances 0.000 description 28
239000000499 gel Substances 0.000 description 25
239000007787 solid Substances 0.000 description 24
239000000126 substance Substances 0.000 description 18
125000004432 carbon atom Chemical group C* 0.000 description 17
150000002191 fatty alcohols Chemical class 0.000 description 16
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 14
229940088598 enzyme Drugs 0.000 description 14
238000005406 washing Methods 0.000 description 14
238000009472 formulation Methods 0.000 description 11
229940014800 succinic anhydride Drugs 0.000 description 11
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 10
238000000227 grinding Methods 0.000 description 10
230000002378 acidificating effect Effects 0.000 description 9
238000003860 storage Methods 0.000 description 9
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 8
229910019142 PO4 Inorganic materials 0.000 description 8
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical class CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 8
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
235000021317 phosphate Nutrition 0.000 description 8
239000011734 sodium Substances 0.000 description 8
229910052708 sodium Inorganic materials 0.000 description 8
BGRWYDHXPHLNKA-UHFFFAOYSA-N Tetraacetylethylenediamine Chemical compound CC(=O)N(C(C)=O)CCN(C(C)=O)C(C)=O BGRWYDHXPHLNKA-UHFFFAOYSA-N 0.000 description 7
239000004744 fabric Substances 0.000 description 7
239000000463 material Substances 0.000 description 7
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 7
239000010452 phosphate Substances 0.000 description 7
150000007513 acids Chemical class 0.000 description 6
125000003545 alkoxy group Chemical group 0.000 description 6
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
230000036961 partial effect Effects 0.000 description 6
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 5
229920002125 Sokalan® Polymers 0.000 description 5
PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 5
DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 5
239000003513 alkali Substances 0.000 description 5
125000002947 alkylene group Chemical group 0.000 description 5
230000008901 benefit Effects 0.000 description 5
235000012216 bentonite Nutrition 0.000 description 5
239000001768 carboxy methyl cellulose Substances 0.000 description 5
239000007795 chemical reaction product Substances 0.000 description 5
235000019441 ethanol Nutrition 0.000 description 5
150000002903 organophosphorus compounds Chemical class 0.000 description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
239000011591 potassium Substances 0.000 description 5
229910052700 potassium Inorganic materials 0.000 description 5
235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 5
229920001027 sodium carboxymethylcellulose Polymers 0.000 description 5
239000000243 solution Substances 0.000 description 5
PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 5
235000021286 stilbenes Nutrition 0.000 description 5
239000010457 zeolite Substances 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
229910052799 carbon Inorganic materials 0.000 description 4
239000006185 dispersion Substances 0.000 description 4
239000000975 dye Substances 0.000 description 4
239000004615 ingredient Substances 0.000 description 4
238000002156 mixing Methods 0.000 description 4
150000002978 peroxides Chemical class 0.000 description 4
229920003023 plastic Polymers 0.000 description 4
239000004033 plastic Substances 0.000 description 4
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 4
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 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
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
229920002134 Carboxymethyl cellulose Polymers 0.000 description 3
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
108091005804 Peptidases Proteins 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
150000005215 alkyl ethers Chemical class 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
239000011575 calcium Substances 0.000 description 3
229910052791 calcium Inorganic materials 0.000 description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
235000010948 carboxy methyl cellulose Nutrition 0.000 description 3
150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
239000000470 constituent Substances 0.000 description 3
238000000354 decomposition reaction Methods 0.000 description 3
230000000694 effects Effects 0.000 description 3
238000007046 ethoxylation reaction Methods 0.000 description 3
230000002209 hydrophobic effect Effects 0.000 description 3
239000003112 inhibitor Substances 0.000 description 3
108010003855 mesentericopeptidase Proteins 0.000 description 3
238000003801 milling Methods 0.000 description 3
239000000049 pigment Substances 0.000 description 3
235000021395 porridge Nutrition 0.000 description 3
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
SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
ZNBNBTIDJSKEAM-UHFFFAOYSA-N 4-[7-hydroxy-2-[5-[5-[6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-3-methyloxolan-2-yl]-5-methyloxolan-2-yl]-2,8-dimethyl-1,10-dioxaspiro[4.5]decan-9-yl]-2-methyl-3-propanoyloxypentanoic acid Chemical compound C1C(O)C(C)C(C(C)C(OC(=O)CC)C(C)C(O)=O)OC11OC(C)(C2OC(C)(CC2)C2C(CC(O2)C2C(CC(C)C(O)(CO)O2)C)C)CC1 ZNBNBTIDJSKEAM-UHFFFAOYSA-N 0.000 description 2
FUXZRRZSHWQAAA-UHFFFAOYSA-N 5,5-dioxodibenzothiophene-3,7-diamine Chemical compound C1=C(N)C=C2S(=O)(=O)C3=CC(N)=CC=C3C2=C1 FUXZRRZSHWQAAA-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
239000004382 Amylase Substances 0.000 description 2
102000013142 Amylases Human genes 0.000 description 2
108010065511 Amylases Proteins 0.000 description 2
102000016938 Catalase Human genes 0.000 description 2
108010053835 Catalase Proteins 0.000 description 2
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
102000035195 Peptidases Human genes 0.000 description 2
229920002257 Plurafac® Polymers 0.000 description 2
229930182556 Polyacetal Natural products 0.000 description 2
239000002202 Polyethylene glycol Substances 0.000 description 2
239000004721 Polyphenylene oxide Substances 0.000 description 2
239000004365 Protease Substances 0.000 description 2
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
150000001447 alkali salts Chemical class 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
235000019418 amylase Nutrition 0.000 description 2
150000008064 anhydrides Chemical class 0.000 description 2
239000003945 anionic surfactant Substances 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
239000000440 bentonite Substances 0.000 description 2
229910000278 bentonite Inorganic materials 0.000 description 2
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
150000007942 carboxylates Chemical class 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
230000007423 decrease Effects 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
229940090960 diethylenetriamine pentamethylene phosphonic acid Drugs 0.000 description 2
238000009826 distribution Methods 0.000 description 2
DUYCTCQXNHFCSJ-UHFFFAOYSA-N dtpmp Chemical compound OP(=O)(O)CN(CP(O)(O)=O)CCN(CP(O)(=O)O)CCN(CP(O)(O)=O)CP(O)(O)=O DUYCTCQXNHFCSJ-UHFFFAOYSA-N 0.000 description 2
230000032050 esterification Effects 0.000 description 2
238000005886 esterification reaction Methods 0.000 description 2
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
229940071106 ethylenediaminetetraacetate Drugs 0.000 description 2
239000012530 fluid Substances 0.000 description 2
150000002430 hydrocarbons Chemical group 0.000 description 2
229910000378 hydroxylammonium sulfate Inorganic materials 0.000 description 2
229920003063 hydroxymethyl cellulose Polymers 0.000 description 2
229940031574 hydroxymethyl cellulose Drugs 0.000 description 2
238000010348 incorporation Methods 0.000 description 2
230000002401 inhibitory effect Effects 0.000 description 2
230000003993 interaction Effects 0.000 description 2
230000004048 modification Effects 0.000 description 2
238000012986 modification Methods 0.000 description 2
229910052901 montmorillonite Inorganic materials 0.000 description 2
MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical class OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
238000005457 optimization Methods 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229960003330 pentetic acid Drugs 0.000 description 2
150000004965 peroxy acids Chemical class 0.000 description 2
125000005342 perphosphate group Chemical group 0.000 description 2
238000005191 phase separation Methods 0.000 description 2
150000003014 phosphoric acid esters Chemical class 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
229920000570 polyether Polymers 0.000 description 2
229920001223 polyethylene glycol Polymers 0.000 description 2
229920006324 polyoxymethylene Polymers 0.000 description 2
229920001296 polysiloxane Polymers 0.000 description 2
159000000001 potassium salts Chemical class 0.000 description 2
230000002265 prevention Effects 0.000 description 2
229960001922 sodium perborate Drugs 0.000 description 2
YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 2
239000007858 starting material Substances 0.000 description 2
239000001384 succinic acid Substances 0.000 description 2
ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 2
239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 2
239000002562 thickening agent Substances 0.000 description 2
238000012549 training Methods 0.000 description 2
150000003852 triazoles Chemical class 0.000 description 2
HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical class [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 2
235000014101 wine Nutrition 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 1
MXVMODFDROLTFD-UHFFFAOYSA-N 2-[2-[2-(2-butoxyethoxy)ethoxy]ethoxy]ethanol Chemical compound CCCCOCCOCCOCCOCCO MXVMODFDROLTFD-UHFFFAOYSA-N 0.000 description 1
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
YTZPUTADNGREHA-UHFFFAOYSA-N 2h-benzo[e]benzotriazole Chemical class C1=CC2=CC=CC=C2C2=NNN=C21 YTZPUTADNGREHA-UHFFFAOYSA-N 0.000 description 1
BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-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
MXMWUQAFMKOTIQ-UHFFFAOYSA-N 4-(carboxymethoxy)-4-oxobutanoic acid Chemical class OC(=O)CCC(=O)OCC(O)=O MXMWUQAFMKOTIQ-UHFFFAOYSA-N 0.000 description 1
ZFXPBTZXYNIAJW-UHFFFAOYSA-N 4-[2-(2-phenylethenyl)phenyl]triazine Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1C1=CC=NN=N1 ZFXPBTZXYNIAJW-UHFFFAOYSA-N 0.000 description 1
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 1
NCCFHSBQJYDEJE-UHFFFAOYSA-N 6-(1,2-dianilino-2-phenylethenyl)-2,3-dimorpholin-4-ylbenzenesulfonic acid Chemical compound C1COCCN1C2=C(C(=C(C=C2)C(=C(C3=CC=CC=C3)NC4=CC=CC=C4)NC5=CC=CC=C5)S(=O)(=O)O)N6CCOCC6 NCCFHSBQJYDEJE-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical class CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 1
238000012935 Averaging Methods 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
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JQVUAIXYUJWPHM-UHFFFAOYSA-N C(C)(=O)O.C(C1=CC=CC=C1)(=O)O.C=C Chemical group C(C)(=O)O.C(C1=CC=CC=C1)(=O)O.C=C JQVUAIXYUJWPHM-UHFFFAOYSA-N 0.000 description 1
125000006539 C12 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])C([H])([H])* 0.000 description 1
BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical group [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
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102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
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239000004115 Sodium Silicate Substances 0.000 description 1
UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
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229910052783 alkali metal Inorganic materials 0.000 description 1
229910052910 alkali metal silicate Inorganic materials 0.000 description 1
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JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
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239000008365 aqueous carrier Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
238000010936 aqueous wash Methods 0.000 description 1
IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
229910021538 borax Inorganic materials 0.000 description 1
150000001642 boronic acid derivatives Chemical class 0.000 description 1
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
229910001424 calcium ion Inorganic materials 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
229910000389 calcium phosphate Inorganic materials 0.000 description 1
235000011010 calcium phosphates Nutrition 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
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238000005341 cation exchange Methods 0.000 description 1
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235000016213 coffee Nutrition 0.000 description 1
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HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
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UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
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125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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238000001879 gelation Methods 0.000 description 1
125000000268 heptanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000005842 heteroatom Chemical group 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
229940051250 hexylene glycol Drugs 0.000 description 1
125000001165 hydrophobic group Chemical group 0.000 description 1
150000002443 hydroxylamines Chemical class 0.000 description 1
239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
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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
229910010272 inorganic material Inorganic materials 0.000 description 1
239000011147 inorganic material Substances 0.000 description 1
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150000008040 ionic compounds Chemical class 0.000 description 1
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NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
235000019421 lipase Nutrition 0.000 description 1
239000006194 liquid suspension Substances 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
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230000014759 maintenance of location Effects 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
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239000002524 monosodium citrate Substances 0.000 description 1
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238000006386 neutralization reaction Methods 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
239000003002 pH adjusting agent Substances 0.000 description 1
239000006174 pH buffer Substances 0.000 description 1
230000020477 pH reduction Effects 0.000 description 1
229940055729 papain Drugs 0.000 description 1
235000019834 papain Nutrition 0.000 description 1
HJKYXKSLRZKNSI-UHFFFAOYSA-I pentapotassium;hydrogen sulfate;oxido sulfate;sulfuric acid Chemical compound [K+].[K+].[K+].[K+].[K+].OS([O-])(=O)=O.[O-]S([O-])(=O)=O.OS(=O)(=O)O[O-].OS(=O)(=O)O[O-] HJKYXKSLRZKNSI-UHFFFAOYSA-I 0.000 description 1
229940111202 pepsin Drugs 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
229920000141 poly(maleic anhydride) Polymers 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000867 polyelectrolyte Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
235000007686 potassium Nutrition 0.000 description 1
235000019353 potassium silicate Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002243 precursor Substances 0.000 description 1
125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
235000019419 proteases Nutrition 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
230000002829 reductive effect Effects 0.000 description 1
239000004576 sand Substances 0.000 description 1
150000003333 secondary alcohols Chemical class 0.000 description 1
238000000926 separation method Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
235000015424 sodium Nutrition 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
235000017550 sodium carbonate Nutrition 0.000 description 1
239000001509 sodium citrate Substances 0.000 description 1
FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
229940048086 sodium pyrophosphate Drugs 0.000 description 1
235000018341 sodium sesquicarbonate Nutrition 0.000 description 1
229910000031 sodium sesquicarbonate Inorganic materials 0.000 description 1
235000019351 sodium silicates Nutrition 0.000 description 1
HELHAJAZNSDZJO-UHFFFAOYSA-L sodium tartrate Chemical class [Na+].[Na+].[O-]C(=O)C(O)C(O)C([O-])=O HELHAJAZNSDZJO-UHFFFAOYSA-L 0.000 description 1
235000010339 sodium tetraborate Nutrition 0.000 description 1
239000004328 sodium tetraborate Substances 0.000 description 1
MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000012265 solid product Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000004071 soot Substances 0.000 description 1
238000001179 sorption measurement Methods 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000013589 supplement Substances 0.000 description 1
150000003892 tartrate salts Chemical class 0.000 description 1
235000013616 tea 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
RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical compound C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 description 1
JZBRFIUYUGTUGG-UHFFFAOYSA-J tetrapotassium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [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
RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 description 1
235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
229930192474 thiophene Natural products 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
JEVFKQIDHQGBFB-UHFFFAOYSA-K tripotassium;2-[bis(carboxylatomethyl)amino]acetate Chemical compound [K+].[K+].[K+].[O-]C(=O)CN(CC([O-])=O)CC([O-])=O JEVFKQIDHQGBFB-UHFFFAOYSA-K 0.000 description 1
229940038773 trisodium citrate Drugs 0.000 description 1
WCTAGTRAWPDFQO-UHFFFAOYSA-K trisodium;hydrogen carbonate;carbonate Chemical compound [Na+].[Na+].[Na+].OC([O-])=O.[O-]C([O-])=O WCTAGTRAWPDFQO-UHFFFAOYSA-K 0.000 description 1
239000012588 trypsin Substances 0.000 description 1
229960001322 trypsin Drugs 0.000 description 1
238000009736 wetting Methods 0.000 description 1
238000004383 yellowing Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3947—Liquid 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0004—Non aqueous liquid compositions comprising insoluble particles

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)
Inorganic Chemistry (AREA)
Detergent Compositions (AREA)

CH3402/87A 1986-09-09 1987-09-04 CH675251A5 (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US90521186A	1986-09-09	1986-09-09

Publications (1)

Publication Number	Publication Date
CH675251A5 true CH675251A5 (no)	1990-09-14

Family

ID=25420433

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH3402/87A CH675251A5 (no)	1986-09-09	1987-09-04

Country Status (16)

Country	Link
JP (1)	JPS6372800A (no)
AU (1)	AU601762B2 (no)
BE (1)	BE1001772A5 (no)
CH (1)	CH675251A5 (no)
DE (1)	DE3729074A1 (no)
DK (1)	DK468787A (no)
FR (1)	FR2603605B1 (no)
GB (1)	GB2195125B (no)
IL (1)	IL83674A (no)
IT (1)	IT1211761B (no)
LU (1)	LU86991A1 (no)
MY (1)	MY102524A (no)
NL (1)	NL8702062A (no)
NZ (1)	NZ221555A (no)
SE (1)	SE8703421L (no)
ZA (1)	ZA876372B (no)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NZ221505A (en) *	1986-09-09	1989-08-29	Colgate Palmolive Co	Liquid detergent compositions with peroxygen bleach and calcium cyanamide activator
GB8625974D0 (en) *	1986-10-30	1986-12-03	Unilever Plc	Non-aqueous liquid detergent
US4892673A (en) *	1988-05-02	1990-01-09	Colgate-Palmolive Company	Non-aqueous, nonionic heavy duty laundry detergent with improved stability
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
DE3842007A1 (de) *	1988-12-14	1990-06-21	Henkel Kgaa	Fluessiges bis pastoeses, bleichmittelhaltiges waschmittel
EP0521863B1 (en) *	1990-03-28	1994-05-18	Unilever Plc	Liquid cleaning products
MX9702315A (es) *	1994-09-26	1997-06-28	Procter & Gamble	Composiciones detergentes liquidas que contienen blanqueador no acuosas.
WO2001023274A1 (en)	1999-09-30	2001-04-05	The Procter & Gamble Company	Detergent package with means to mask amine malodours
DE10140786A1 (de)	2001-08-20	2003-03-06	Haarmann & Reimer Gmbh	Depotpräparate
JP5058570B2 (ja) *	2005-11-30	2012-10-24	ライオン株式会社	殺ダニ方法
US8871807B2 (en)	2008-03-28	2014-10-28	Ecolab Usa Inc.	Detergents capable of cleaning, bleaching, sanitizing and/or disinfecting textiles including sulfoperoxycarboxylic acids
US9321664B2 (en)	2011-12-20	2016-04-26	Ecolab Usa Inc.	Stable percarboxylic acid compositions and uses thereof
US9242879B2 (en)	2012-03-30	2016-01-26	Ecolab Usa Inc.	Use of peracetic acid/hydrogen peroxide and peroxide-reducing agents for treatment of drilling fluids, frac fluids, flowback water and disposal water
US10165774B2 (en)	2013-03-05	2019-01-01	Ecolab Usa Inc.	Defoamer useful in a peracid composition with anionic surfactants
US20140256811A1 (en)	2013-03-05	2014-09-11	Ecolab Usa Inc.	Efficient stabilizer in controlling self accelerated decomposition temperature of peroxycarboxylic acid compositions with mineral acids
US8822719B1 (en)	2013-03-05	2014-09-02	Ecolab Usa Inc.	Peroxycarboxylic acid compositions suitable for inline optical or conductivity monitoring
US12096768B2 (en)	2019-08-07	2024-09-24	Ecolab Usa Inc.	Polymeric and solid-supported chelators for stabilization of peracid-containing compositions

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4283301A (en) *	1980-07-02	1981-08-11	The Procter & Gamble Company	Bleaching process and compositions
DE3465334D1 (en) *	1983-04-14	1987-09-17	Interox Chemicals Ltd	Peroxygen compounds
GB8310080D0 (en) *	1983-04-14	1983-05-18	Interox Chemicals Ltd	Bleach composition
GB8328654D0 (en) *	1983-10-26	1983-11-30	Interox Chemicals Ltd	Hydrogen peroxide compositions
ZA852197B (en) *	1984-04-06	1986-11-26	Colgate Palmolive Co	Liquid laundry detergent composition containing polyphosphate
EP0195663A3 (en) *	1985-03-20	1987-05-13	The Procter & Gamble Company	Bleaching compositions
MX162823B (es) *	1985-03-29	1991-06-28	Colgate Palmolive Co	Mejoras a composicion de detergente blanqueadora liquida para lavar ropa
EP0217454B1 (en) *	1985-09-30	1992-03-11	Unilever N.V.	Non-aqueous liquid detergent composition and perborate anhydrous
US4772413A (en) *	1986-08-28	1988-09-20	Colgate-Palmolive Company	Nonaqueous liquid nonbuilt laundry detergent bleach booster composition containing diacetyl methyl amine and method of use

1987
- 1987-08-24 NZ NZ221555A patent/NZ221555A/xx unknown
- 1987-08-26 ZA ZA876372A patent/ZA876372B/xx unknown
- 1987-08-27 AU AU77498/87A patent/AU601762B2/en not_active Ceased
- 1987-08-28 MY MYPI87001467A patent/MY102524A/en unknown
- 1987-08-28 IL IL83674A patent/IL83674A/xx not_active IP Right Cessation
- 1987-09-01 DE DE19873729074 patent/DE3729074A1/de not_active Ceased
- 1987-09-02 NL NL8702062A patent/NL8702062A/nl not_active Application Discontinuation
- 1987-09-03 SE SE8703421A patent/SE8703421L/ not_active Application Discontinuation
- 1987-09-04 CH CH3402/87A patent/CH675251A5/de not_active IP Right Cessation
- 1987-09-08 DK DK468787A patent/DK468787A/da not_active Application Discontinuation
- 1987-09-08 BE BE8701008A patent/BE1001772A5/fr not_active IP Right Cessation
- 1987-09-08 IT IT8748365A patent/IT1211761B/it active
- 1987-09-08 GB GB8721062A patent/GB2195125B/en not_active Expired - Lifetime
- 1987-09-09 FR FR8712527A patent/FR2603605B1/fr not_active Expired - Fee Related
- 1987-09-09 JP JP62226225A patent/JPS6372800A/ja active Pending
- 1987-09-09 LU LU86991A patent/LU86991A1/fr unknown

Also Published As

Publication number	Publication date
DK468787A (da)	1988-03-10
AU601762B2 (en)	1990-09-20
DE3729074A1 (de)	1988-03-17
SE8703421D0 (sv)	1987-09-03
BE1001772A5 (fr)	1990-03-06
SE8703421L (sv)	1988-03-10
FR2603605A1 (fr)	1988-03-11
LU86991A1 (fr)	1988-03-02
AU7749887A (en)	1988-03-17
IL83674A (en)	1991-07-18
ZA876372B (en)	1989-04-26
NL8702062A (nl)	1988-04-05
GB2195125A (en)	1988-03-30
IL83674A0 (en)	1988-01-31
DK468787D0 (da)	1987-09-08
NZ221555A (en)	1989-08-29
GB2195125B (en)	1991-05-15
JPS6372800A (ja)	1988-04-02
GB8721062D0 (en)	1987-10-14
IT8748365A0 (it)	1987-09-08
FR2603605B1 (fr)	1993-07-30
MY102524A (en)	1992-07-31
IT1211761B (it)	1989-11-03

Publication	Publication Date	Title
AT395165B (de)	1992-10-12	Nicht-waesseriges, fluessiges waschmittel
AT395166B (de)	1992-10-12	Vollwaschmittel
AT396114B (de)	1993-06-25	Waschmittel
AT394390B (de)	1992-03-25	Fluessige vollwaschmittelzusammensetzung
DE3728256A1 (de)	1988-03-10	Nicht-waessrige fluessige bleichmittelverstaerkende zusammensetzung
CH674371A5 (no)	1990-05-31
CH671234A5 (no)	1989-08-15
CH676993A5 (no)	1991-03-28
CH672498A5 (no)	1989-11-30
AT396113B (de)	1993-06-25	Nicht-waesseriges fluessiges grobwaschmittel
DE3728047A1 (de)	1988-03-17	Zusammensetzung zum behandeln und reinigen von textilien, diese enthaltendes vollwaschmittel und anwendung
CH675251A5 (no)	1990-09-14
CH678533A5 (no)	1991-09-30
AT395168B (de)	1992-10-12	Nichtwaesseriges fluessiges grobwaschmittel
DE3704876A1 (de)	1987-08-27	Vollwaschmittelzusammensetzung
AT398431B (de)	1994-12-27	Nicht-wässeriges flüssiges waschmittel
CH675428A5 (no)	1990-09-28
DE3609345C2 (de)	1996-11-21	Flüssiges Textilwasch- und Bleichmittel und Reinigungsverfahren damit
DE3727793A1 (de)	1988-03-10	In hohem masse bioabbaubare nichtionische tenside, diese enthaltende waschmittel und deren anwendung
CH675589A5 (no)	1990-10-15
DE3625256A1 (de)	1987-02-05	Phosphatfreies oder gering phosphathaltiges waschmittel
CH674850A5 (no)	1990-07-31

Legal Events

Date	Code	Title	Description
1994-05-31	PL	Patent ceased
2024-10-31	PL	Patent ceased