PH26725A - Bleaching compounds and compositions comprising fatty peroxyacids salts thereof and precursors therefor having amide moieties in the fatty chain - Google Patents

Bleaching compounds and compositions comprising fatty peroxyacids salts thereof and precursors therefor having amide moieties in the fatty chain Download PDF

Info

Publication number: PH26725A
Authority: PH; Philippines
Prior art keywords: group; alkyl; bleaching; carbon atoms; compound
Prior art date: 1987-05-08

Application number

PH36889A

Other languages

English (en)

Inventor

Michael Eugene Burns

Frederick Edward Hardy

Original Assignee

Michael Eugene Burns

Frederick Edward Hardy

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.)

1987-05-08

Filing date

1988-05-04

Publication date

1992-09-28

1988-05-04 Application filed by Michael Eugene Burns, Frederick Edward Hardy filed Critical Michael Eugene Burns

1992-09-28 Publication of PH26725A publication Critical patent/PH26725A/en

Links

238000004061 bleaching Methods 0.000 title claims abstract description 63
239000000203 mixture Substances 0.000 title claims abstract description 63
150000001875 compounds Chemical class 0.000 title claims abstract description 41
150000001408 amides Chemical group 0.000 title abstract description 8
-1 peroxyacids salts Chemical class 0.000 title description 28
239000002243 precursor Substances 0.000 title description 2
239000007844 bleaching agent Substances 0.000 claims abstract description 40
239000003599 detergent Substances 0.000 claims abstract description 24
150000004965 peroxy acids Chemical class 0.000 claims abstract description 23
239000004753 textile Substances 0.000 claims abstract description 14
125000004432 carbon atom Chemical group C* 0.000 claims description 49
125000000217 alkyl group Chemical group 0.000 claims description 42
239000012190 activator Substances 0.000 claims description 29
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 22
239000000243 solution Substances 0.000 claims description 22
239000011734 sodium Substances 0.000 claims description 16
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group 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 claims description 15
229910052708 sodium Inorganic materials 0.000 claims description 15
239000002253 acid Substances 0.000 claims description 14
125000003118 aryl group Chemical group 0.000 claims description 14
229910052799 carbon Inorganic materials 0.000 claims description 11
239000004094 surface-active agent Substances 0.000 claims description 11
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 10
125000002877 alkyl aryl group Chemical group 0.000 claims description 10
229910052700 potassium Chemical group 0.000 claims description 9
239000011591 potassium Chemical group 0.000 claims description 9
150000001450 anions Chemical class 0.000 claims description 8
239000007864 aqueous solution Substances 0.000 claims description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 6
238000000034 method Methods 0.000 claims description 6
230000003381 solubilizing effect Effects 0.000 claims description 5
150000001768 cations Chemical class 0.000 claims description 4
PEYZZYZIHZNZHH-UHFFFAOYSA-L magnesium;oxido formate Chemical compound [Mg+2].[O-]OC=O.[O-]OC=O PEYZZYZIHZNZHH-UHFFFAOYSA-L 0.000 claims description 4
125000004429 atom Chemical group 0.000 claims description 3
ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 claims 2
229960002163 hydrogen peroxide Drugs 0.000 claims 2
UNILWMWFPHPYOR-KXEYIPSPSA-M 1-[6-[2-[3-[3-[3-[2-[2-[3-[[2-[2-[[(2r)-1-[[2-[[(2r)-1-[3-[2-[2-[3-[[2-(2-amino-2-oxoethoxy)acetyl]amino]propoxy]ethoxy]ethoxy]propylamino]-3-hydroxy-1-oxopropan-2-yl]amino]-2-oxoethyl]amino]-3-[(2r)-2,3-di(hexadecanoyloxy)propyl]sulfanyl-1-oxopropan-2-yl Chemical compound O=C1C(SCCC(=O)NCCCOCCOCCOCCCNC(=O)COCC(=O)N[C@@H](CSC[C@@H](COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)C(=O)NCC(=O)N[C@H](CO)C(=O)NCCCOCCOCCOCCCNC(=O)COCC(N)=O)CC(=O)N1CCNC(=O)CCCCCN\1C2=CC=C(S([O-])(=O)=O)C=C2CC/1=C/C=C/C=C/C1=[N+](CC)C2=CC=C(S([O-])(=O)=O)C=C2C1 UNILWMWFPHPYOR-KXEYIPSPSA-M 0.000 claims 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 1
235000002918 Fraxinus excelsior Nutrition 0.000 claims 1
239000002956 ash Substances 0.000 claims 1
239000012267 brine Substances 0.000 claims 1
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 claims 1
230000002209 hydrophobic effect Effects 0.000 abstract description 5
229920001296 polysiloxane Polymers 0.000 description 13
239000003795 chemical substances by application Substances 0.000 description 12
239000004744 fabric Substances 0.000 description 12
239000002689 soil Substances 0.000 description 11
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical group O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
VZCYOOQTPOCHFL-OWOJBTEDSA-N fumaric acid group Chemical group C(\C=C\C(=O)O)(=O)O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 10
FJDUDHYHRVPMJZ-UHFFFAOYSA-N nonan-1-amine Chemical compound CCCCCCCCCN FJDUDHYHRVPMJZ-UHFFFAOYSA-N 0.000 description 10
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
239000000463 material Substances 0.000 description 9
150000003839 salts Chemical class 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 7
239000008187 granular material Substances 0.000 description 7
239000007787 solid Substances 0.000 description 7
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 7
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
239000001301 oxygen Substances 0.000 description 6
229910052760 oxygen Inorganic materials 0.000 description 6
239000000344 soap Substances 0.000 description 6
108090000790 Enzymes Proteins 0.000 description 5
102000004190 Enzymes Human genes 0.000 description 5
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
125000002947 alkylene group Chemical group 0.000 description 5
230000001276 controlling effect Effects 0.000 description 5
229940088598 enzyme Drugs 0.000 description 5
125000004494 ethyl ester group Chemical group 0.000 description 5
239000001530 fumaric acid Substances 0.000 description 5
238000002844 melting Methods 0.000 description 5
230000008018 melting Effects 0.000 description 5
230000000269 nucleophilic effect Effects 0.000 description 5
239000000377 silicon dioxide Substances 0.000 description 5
238000003860 storage Methods 0.000 description 5
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
125000001931 aliphatic group Chemical group 0.000 description 4
239000003945 anionic surfactant Substances 0.000 description 4
235000019864 coconut oil Nutrition 0.000 description 4
239000003240 coconut oil Substances 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
230000000694 effects Effects 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
150000004665 fatty acids Chemical class 0.000 description 4
239000004615 ingredient Substances 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
239000003760 tallow Substances 0.000 description 4
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
238000005406 washing Methods 0.000 description 4
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 3
BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical group [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 3
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
SCKXCAADGDQQCS-UHFFFAOYSA-N Performic acid Chemical compound OOC=O SCKXCAADGDQQCS-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
229910052783 alkali metal Inorganic materials 0.000 description 3
150000001340 alkali metals Chemical class 0.000 description 3
239000006172 buffering agent Substances 0.000 description 3
229910001424 calcium ion Inorganic materials 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
230000000875 corresponding effect Effects 0.000 description 3
238000004090 dissolution Methods 0.000 description 3
239000003925 fat Substances 0.000 description 3
235000019197 fats Nutrition 0.000 description 3
125000002768 hydroxyalkyl group Chemical group 0.000 description 3
238000005342 ion exchange Methods 0.000 description 3
239000011777 magnesium Substances 0.000 description 3
229910052749 magnesium Inorganic materials 0.000 description 3
235000001055 magnesium Nutrition 0.000 description 3
229940091250 magnesium supplement Drugs 0.000 description 3
239000004200 microcrystalline wax Substances 0.000 description 3
235000019808 microcrystalline wax Nutrition 0.000 description 3
239000002736 nonionic surfactant Substances 0.000 description 3
239000003921 oil Substances 0.000 description 3
235000019198 oils Nutrition 0.000 description 3
159000000001 potassium salts Chemical class 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000001993 wax Substances 0.000 description 3
XSVSPKKXQGNHMD-UHFFFAOYSA-N 5-bromo-3-methyl-1,2-thiazole Chemical compound CC=1C=C(Br)SN=1 XSVSPKKXQGNHMD-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
229910000503 Na-aluminosilicate Inorganic materials 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
108010056079 Subtilisins Proteins 0.000 description 2
102000005158 Subtilisins Human genes 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
125000002252 acyl group Chemical group 0.000 description 2
150000001335 aliphatic alkanes Chemical class 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
239000013078 crystal Substances 0.000 description 2
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 2
238000001035 drying Methods 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000001914 filtration Methods 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical class CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
229910003002 lithium salt Inorganic materials 0.000 description 2
159000000002 lithium salts Chemical class 0.000 description 2
159000000003 magnesium salts Chemical class 0.000 description 2
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
239000011976 maleic acid Substances 0.000 description 2
YDSWCNNOKPMOTP-UHFFFAOYSA-N mellitic acid Chemical compound 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
239000003607 modifier Substances 0.000 description 2
235000002949 phytic acid Nutrition 0.000 description 2
239000000047 product Substances 0.000 description 2
CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 2
238000007127 saponification reaction Methods 0.000 description 2
235000015067 sauces Nutrition 0.000 description 2
235000012217 sodium aluminium silicate Nutrition 0.000 description 2
229910000029 sodium carbonate Inorganic materials 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
238000006467 substitution reaction Methods 0.000 description 2
150000004685 tetrahydrates Chemical class 0.000 description 2
DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 description 1
CIOXZGOUEYHNBF-UHFFFAOYSA-N (carboxymethoxy)succinic acid Chemical compound OC(=O)COC(C(O)=O)CC(O)=O CIOXZGOUEYHNBF-UHFFFAOYSA-N 0.000 description 1
FSQQTNAZHBEJLS-OWOJBTEDSA-N (e)-4-amino-4-oxobut-2-enoic acid Chemical class NC(=O)\C=C\C(O)=O FSQQTNAZHBEJLS-OWOJBTEDSA-N 0.000 description 1
XLYMOEINVGRTEX-ONEGZZNKSA-N (e)-4-ethoxy-4-oxobut-2-enoic acid Chemical compound CCOC(=O)\C=C\C(O)=O XLYMOEINVGRTEX-ONEGZZNKSA-N 0.000 description 1
RIZUCYSQUWMQLX-UHFFFAOYSA-N 2,3-dimethylbenzoic acid Chemical compound CC1=CC=CC(C(O)=O)=C1C RIZUCYSQUWMQLX-UHFFFAOYSA-N 0.000 description 1
XYJLPCAKKYOLGU-UHFFFAOYSA-N 2-phosphonoethylphosphonic acid Chemical class OP(O)(=O)CCP(O)(O)=O XYJLPCAKKYOLGU-UHFFFAOYSA-N 0.000 description 1
GONFBOIJNUKKST-UHFFFAOYSA-N 5-ethylsulfanyl-2h-tetrazole Chemical compound CCSC=1N=NNN=1 GONFBOIJNUKKST-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical group CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
108010065511 Amylases Proteins 0.000 description 1
102000013142 Amylases Human genes 0.000 description 1
102100023006 Basic leucine zipper transcriptional factor ATF-like 2 Human genes 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
101100435497 Drosophila melanogaster ari-1 gene Proteins 0.000 description 1
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical class OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
241001553290 Euphorbia antisyphilitica Species 0.000 description 1
101000903615 Homo sapiens Basic leucine zipper transcriptional factor ATF-like 2 Proteins 0.000 description 1
IMQLKJBTEOYOSI-GPIVLXJGSA-N Inositol-hexakisphosphate Chemical class OP(O)(=O)O[C@H]1[C@H](OP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O IMQLKJBTEOYOSI-GPIVLXJGSA-N 0.000 description 1
244000234179 Myrtus ugni Species 0.000 description 1
235000012093 Myrtus ugni Nutrition 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
108091005804 Peptidases Proteins 0.000 description 1
102000035195 Peptidases Human genes 0.000 description 1
235000014676 Phragmites communis Nutrition 0.000 description 1
IMQLKJBTEOYOSI-UHFFFAOYSA-N Phytic acid Natural products OP(O)(=O)OC1C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C1OP(O)(O)=O IMQLKJBTEOYOSI-UHFFFAOYSA-N 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Chemical class OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
235000003095 Vaccinium corymbosum Nutrition 0.000 description 1
240000000851 Vaccinium corymbosum Species 0.000 description 1
235000017537 Vaccinium myrtillus Nutrition 0.000 description 1
229910021536 Zeolite Inorganic materials 0.000 description 1
MEESPVWIOBCLJW-KTKRTIGZSA-N [(z)-octadec-9-enyl] dihydrogen phosphate Chemical compound CCCCCCCC\C=C/CCCCCCCCOP(O)(O)=O MEESPVWIOBCLJW-KTKRTIGZSA-N 0.000 description 1
ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
150000008041 alkali metal carbonates Chemical class 0.000 description 1
150000004973 alkali metal peroxides Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
125000005192 alkyl ethylene group Chemical class 0.000 description 1
229910000323 aluminium silicate Inorganic materials 0.000 description 1
125000003368 amide group Chemical group 0.000 description 1
235000019418 amylase Nutrition 0.000 description 1
229940025131 amylases Drugs 0.000 description 1
230000003625 amylolytic effect Effects 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
235000021168 barbecue Nutrition 0.000 description 1
235000013871 bee wax Nutrition 0.000 description 1
229940092738 beeswax Drugs 0.000 description 1
239000012166 beeswax Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
235000021014 blueberries Nutrition 0.000 description 1
238000009835 boiling Methods 0.000 description 1
150000001642 boronic acid derivatives Chemical class 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical class O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
239000004203 carnauba wax Substances 0.000 description 1
235000013869 carnauba wax Nutrition 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000003093 cationic surfactant Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
229940000425 combination drug Drugs 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
239000012297 crystallization seed Substances 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
229940079919 digestives enzyme preparation Drugs 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
235000011180 diphosphates Nutrition 0.000 description 1
KRHIGIYZRJWEGL-UHFFFAOYSA-N dodecapotassium;tetraborate Chemical class [K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-] KRHIGIYZRJWEGL-UHFFFAOYSA-N 0.000 description 1
239000000975 dye Substances 0.000 description 1
125000004185 ester group Chemical group 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
XWENCHGJOCJZQO-UHFFFAOYSA-N ethane-1,1,2,2-tetracarboxylic acid Chemical compound OC(=O)C(C(O)=O)C(C(O)=O)C(O)=O XWENCHGJOCJZQO-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
125000005313 fatty acid group Chemical group 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000012065 filter cake Substances 0.000 description 1
239000012530 fluid Substances 0.000 description 1
235000021588 free fatty acids Nutrition 0.000 description 1
229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
239000007789 gas Substances 0.000 description 1
230000002070 germicidal effect Effects 0.000 description 1
239000011521 glass Substances 0.000 description 1
125000005456 glyceride group Chemical group 0.000 description 1
150000004820 halides Chemical group 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
125000000623 heterocyclic group Chemical group 0.000 description 1
125000001183 hydrocarbyl group Chemical group 0.000 description 1
125000001165 hydrophobic group Chemical group 0.000 description 1
239000003752 hydrotrope Substances 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
108010003855 mesentericopeptidase Proteins 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000005341 metaphosphate group Chemical group 0.000 description 1
229940098779 methanesulfonic acid Drugs 0.000 description 1
JZMJDSHXVKJFKW-UHFFFAOYSA-N methyl sulfate Chemical group COS(O)(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-N 0.000 description 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
150000004682 monohydrates Chemical class 0.000 description 1
239000012170 montan wax Substances 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
UHGIMQLJWRAPLT-UHFFFAOYSA-N octadecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCCCOP(O)(O)=O UHGIMQLJWRAPLT-UHFFFAOYSA-N 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
239000010502 orange oil Substances 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000005486 organic electrolyte Substances 0.000 description 1
150000001451 organic peroxides Chemical class 0.000 description 1
MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
239000012188 paraffin wax Chemical class 0.000 description 1
239000002245 particle Substances 0.000 description 1
230000035515 penetration Effects 0.000 description 1
239000002304 perfume Substances 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
125000005342 perphosphate group Chemical group 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
239000000467 phytic acid Substances 0.000 description 1
229940068041 phytic acid Drugs 0.000 description 1
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
229920006324 polyoxymethylene Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000002797 proteolythic effect Effects 0.000 description 1
229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
238000010992 reflux Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
229960001922 sodium perborate Drugs 0.000 description 1
PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
235000019832 sodium triphosphate Nutrition 0.000 description 1
YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
239000002195 soluble material Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000003107 substituted aryl group Chemical group 0.000 description 1
230000001180 sulfating effect Effects 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
150000003462 sulfoxides Chemical class 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
108010075550 termamyl Proteins 0.000 description 1
MSLRPWGRFCKNIZ-UHFFFAOYSA-J tetrasodium;hydrogen peroxide;dicarbonate Chemical compound [Na+].[Na+].[Na+].[Na+].OO.OO.OO.[O-]C([O-])=O.[O-]C([O-])=O MSLRPWGRFCKNIZ-UHFFFAOYSA-J 0.000 description 1
238000004448 titration Methods 0.000 description 1
150000004684 trihydrates Chemical class 0.000 description 1
FDGZUBKNYGBWHI-UHFFFAOYSA-N trioctadecyl phosphate Chemical class CCCCCCCCCCCCCCCCCCOP(=O)(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC FDGZUBKNYGBWHI-UHFFFAOYSA-N 0.000 description 1
125000001874 trioxidanyl group Chemical group [*]OOO[H] 0.000 description 1
SVETUDAIEHYIKZ-IUPFWZBJSA-N tris[(z)-octadec-9-enyl] phosphate Chemical compound CCCCCCCC\C=C/CCCCCCCCOP(=O)(OCCCCCCCC\C=C/CCCCCCCC)OCCCCCCCC\C=C/CCCCCCCC SVETUDAIEHYIKZ-IUPFWZBJSA-N 0.000 description 1
AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
230000002087 whitening effect Effects 0.000 description 1
239000010457 zeolite Substances 0.000 description 1
239000002888 zwitterionic surfactant Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/40—Peroxy compounds containing nitrogen atoms
- 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
- C11D3/3945—Organic per-compounds

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Inorganic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Detergent Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

PH36889A 1987-05-08 1988-05-04 Bleaching compounds and compositions comprising fatty peroxyacids salts thereof and precursors therefor having amide moieties in the fatty chain PH26725A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US07/047,804 US4852989A (en)	1987-05-08	1987-05-08	Bleaching compounds and compositions comprising fatty peroxyacids salts thereof and precursors therefor having amide moieties in the fatty chain

Publications (1)

Publication Number	Publication Date
PH26725A true PH26725A (en)	1992-09-28

Family

ID=21951065

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PH36889A PH26725A (en)	1987-05-08	1988-05-04	Bleaching compounds and compositions comprising fatty peroxyacids salts thereof and precursors therefor having amide moieties in the fatty chain

Country Status (6)

Country	Link
US (1)	US4852989A (de)
EP (1)	EP0290292B1 (de)
AT (1)	ATE110409T1 (de)
CA (1)	CA1331622C (de)
DE (1)	DE3851177T2 (de)
PH (1)	PH26725A (de)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8830235D0 (en) *	1988-12-24	1989-02-22	Interox Chemicals Ltd	Percarboxylic acids
GB8911957D0 (en) *	1989-05-24	1989-07-12	Interox Chemicals Ltd	Peroxyacid manufacture
GB9018749D0 (en) *	1990-08-28	1990-10-10	Unilever Plc	Bleaching and detergent compositions
EP0504952A1 (de) *	1991-02-15	1992-09-23	The Procter & Gamble Company	Flüssiges stabiles Amidoperoxysäure-Bleichmittel
US5234617A (en) *	1992-04-20	1993-08-10	Kathleen B. Hunter	Aqueous liquid bleach compositions with fluorescent whitening agent and polyvinyl pyrrolidone or polyvinyl alcohol
US5248434A (en) *	1992-04-20	1993-09-28	The Proctor & Gamble Company	Liquid or gel bleaching composition containing amidoperoxyacid bleach and perfume
CA2098353A1 (en) *	1992-06-15	1993-12-16	Yueting Chou	Sulfonamide peroxycarboxylic acids
EP0592033A1 (de) *	1992-10-07	1994-04-13	The Procter & Gamble Company	Verfahren zur Herstellung von Peroxysäure enthaltenden Partikeln
US5409632A (en) *	1992-11-16	1995-04-25	The Procter & Gamble Company	Cleaning and bleaching composition with amidoperoxyacid
US5281746A (en) *	1993-02-01	1994-01-25	Monsanto Company	Process for preparing peroxyacid precursors having amide moieties in the fatty chain
JPH08510778A (ja) *	1993-05-20	1996-11-12	ザ、プロクター、エンド、ギャンブル、カンパニー	アミド部分を有するペルオキシ酸活性剤を含む漂白組成物
CZ305995A3 (en) *	1993-05-20	1996-05-15	Procter & Gamble	Bleaching preparations comprising bleaching agent activators, peroxy acid and enzymes
US5414099A (en) *	1993-09-14	1995-05-09	The Procter & Gamble Company	Synthesis of amido acids from carboxylic acids and lactams
US5932532A (en) *	1993-10-14	1999-08-03	Procter & Gamble Company	Bleach compositions comprising protease enzyme
GB9410225D0 (en) *	1994-05-21	1994-07-06	Procter & Gamble	Detergent compositions having suds suppressing properties
US5523434A (en) *	1995-03-15	1996-06-04	The Procter & Gamble Company	Synthesis of bleach activators
US5837670A (en) *	1995-04-18	1998-11-17	Hartshorn; Richard Timothy	Detergent compositions having suds suppressing properties
US5945392A (en) *	1995-06-20	1999-08-31	Procter & Gamble Company	Nonaqueous, particulate-containing detergent compositions
WO1999009004A2 (en)	1997-08-20	1999-02-25	The Procter & Gamble Company	Process for preparing and/or purifying amido acid phenyl ester sulfonates
US6500973B2 (en)	2000-06-02	2002-12-31	Eastman Chemical Company	Extractive solution crystallization of chemical compounds
US6498124B2 (en)	2000-06-02	2002-12-24	Eastman Chemical Company	Isolation of phenyl ester salts from mixtures comprising sulfolane
DE60108379T2 (de)	2000-06-02	2005-12-22	Eastman Chemical Co., Kingsport	Reinigung von phenylestersalzen
US6660712B2 (en) *	2000-06-02	2003-12-09	Dale Elbert Van Sickle	Stabilization of amido acids with antioxidants
WO2001092209A2 (en)	2000-06-02	2001-12-06	Eastman Chemical Company	Process for hydrolyzing amido-carboxylic acid esters into amido-carboxylic acids

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2043086A1 (de) *	1970-08-31	1972-03-30	Henkel & Cie GmbH, 4000 Dusseldorf	Schwachschaumendes Wasch , Reimgungs und Enthartungsmittel
FR2427326A2 (fr) *	1978-05-31	1979-12-28	Guerbet Sa	Nouveaux derives ioniques polyiodes du benzene, utilisables comme produits opacifiants pour la radiographie
US4283301A (en) *	1980-07-02	1981-08-11	The Procter & Gamble Company	Bleaching process and compositions
ES506859A0 (es) *	1980-11-06	1983-11-01	Procter & Gamble	Un procedimiento para preparar una composicion granular ac- tivadora del blanqueo.
US4443623A (en) *	1982-05-12	1984-04-17	American Cyanamid Company	Preparation of predominately methyl acrylamidoglycolate methyl ether in a normally liquid product
US4623729A (en) *	1982-07-22	1986-11-18	E. R. Squibb & Sons, Inc.	Acylalkylaminocarbonyl substituted amino and imino acid compounds
EP0105689B1 (de) *	1982-09-30	1987-12-09	The Procter & Gamble Company	Magnesiumsalze von Peroxycarbonsäuren
GB8304990D0 (en) *	1983-02-23	1983-03-30	Procter & Gamble	Detergent ingredients
US4525292A (en) *	1983-03-07	1985-06-25	Cushman Mark E	Bleaching detergent compositions comprising sulfosuccinate bleach promoters
US4671891A (en) *	1983-09-16	1987-06-09	The Procter & Gamble Company	Bleaching compositions
US4539130A (en) *	1983-12-22	1985-09-03	The Procter & Gamble Company	Peroxygen bleach activators and bleaching compositions
US4634551A (en) *	1985-06-03	1987-01-06	Procter & Gamble Company	Bleaching compounds and compositions comprising fatty peroxyacids salts thereof and precursors therefor having amide moieties in the fatty chain
GB8415909D0 (en) *	1984-06-21	1984-07-25	Procter & Gamble Ltd	Peracid compounds
US4686063A (en) *	1986-09-12	1987-08-11	The Procter & Gamble Company	Fatty peroxyacids or salts thereof having amide moieties in the fatty chain and low levels of exotherm control agents

1987
- 1987-05-08 US US07/047,804 patent/US4852989A/en not_active Expired - Fee Related
1988
- 1988-05-04 CA CA000565883A patent/CA1331622C/en not_active Expired - Fee Related
- 1988-05-04 PH PH36889A patent/PH26725A/en unknown
- 1988-05-09 AT AT88304168T patent/ATE110409T1/de not_active IP Right Cessation
- 1988-05-09 DE DE3851177T patent/DE3851177T2/de not_active Expired - Fee Related
- 1988-05-09 EP EP88304168A patent/EP0290292B1/de not_active Expired - Lifetime

Also Published As

Publication number	Publication date
ATE110409T1 (de)	1994-09-15
EP0290292A3 (en)	1990-05-23
US4852989A (en)	1989-08-01
DE3851177T2 (de)	1995-03-02
EP0290292B1 (de)	1994-08-24
CA1331622C (en)	1994-08-23
EP0290292A2 (de)	1988-11-09
DE3851177D1 (de)	1994-09-29

Publication	Publication Date	Title
PH26725A (en)	1992-09-28	Bleaching compounds and compositions comprising fatty peroxyacids salts thereof and precursors therefor having amide moieties in the fatty chain
US4634551A (en)	1987-01-06	Bleaching compounds and compositions comprising fatty peroxyacids salts thereof and precursors therefor having amide moieties in the fatty chain
EP0170386B1 (de)	1993-12-08	Bleichmittelverbindungen und Zusammensetzungen, die Peroxyfettsäuren enthalten, deren Salze und deren Vorläufer
US4606838A (en)	1986-08-19	Bleaching compositions comprising alkoxy substituted aromatic peroxyacids
JP2608898B2 (ja)	1997-05-14	脂肪鎖中にアミド部分を有する脂肪ペルオキシ酸またはそれらの塩および少量の発熱制御剤
US4412934A (en)	1983-11-01	Bleaching compositions
EP0062523B1 (de)	1987-12-09	Reinigungszusatzmittel, deren Herstellung und Anwendung in Reinigungsmittelzusammensetzungen
FI71764C (fi)	1987-02-09	Katalytkomposition foer persyreblekmedel som skall anvaendas i en blekmedelssammansaettning foer tvaettinraettningar, blekmedelkomposition innehaollande katalytkomposition och foerfarande foer framstaellning av kompositionen.
US4525292A (en)	1985-06-25	Bleaching detergent compositions comprising sulfosuccinate bleach promoters
JPH0696720B2 (ja)	1994-11-30	漂白剤及び漂白洗浄剤組成物
CA2079487C (en)	1997-01-14	Bleach granules containing an amidoperoxyacid
JP2000500518A (ja)	2000-01-18	繊維漂白組成物
EP0163331A1 (de)	1985-12-04	Körnige Detergens-Bleichmittelzusammensetzungen
JP2914484B2 (ja)	1999-06-28	漂白化合物
EP0195597B1 (de)	1989-11-02	Bleichaktivatoren und diese enthaltende Bleichmittelzusammensetzungen
CA1245222A (en)	1988-11-22	Bleaching compounds and compositions comprising fatty peroxyacids salts thereof and precursors therefor having amide moieties in the fatty chain
JP2538646B2 (ja)	1996-09-25	新規カチオン化合物、それを含有する漂白剤組成物及び漂白洗浄剤組成物
JPH04234498A (ja)	1992-08-24	漂白洗剤組成物
IT8447557A1 (it)	1985-07-18	Composizione di candeggio a bassa temperatura.