IE913949A1 - Granular detergent of bleaching compositions containing¹aminoperoxyacid bleach and perfume - Google Patents

Granular detergent of bleaching compositions containing¹aminoperoxyacid bleach and perfume

Info

Publication number: IE913949A1
Authority: IE; Ireland
Prior art keywords: bleach; weight; perfume; napaa; methyl
Prior art date: 1990-11-14

Application number

IE394991A

Other languages

English (en)

Original Assignee

Procter & Gamble

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.)

1990-11-14

Filing date

1991-11-13

Publication date

1992-05-20

1991-11-13 Application filed by Procter & Gamble filed Critical Procter & Gamble

1992-05-20 Publication of IE913949A1 publication Critical patent/IE913949A1/en

Links

239000002304 perfume Substances 0.000 title claims abstract description 70
239000000203 mixture Substances 0.000 title claims abstract description 69
239000007844 bleaching agent Substances 0.000 title claims abstract description 58
239000003599 detergent Substances 0.000 title claims abstract description 43
238000004061 bleaching Methods 0.000 title claims abstract description 20
239000004615 ingredient Substances 0.000 claims abstract description 36
-1 Exaltex Chemical compound 0.000 claims description 43
239000008187 granular material Substances 0.000 claims description 37
125000004432 carbon atom Chemical group C* 0.000 claims description 32
NTPLXRHDUXRPNE-UHFFFAOYSA-N 4-methoxyacetophenone Chemical compound COC1=CC=C(C(C)=O)C=C1 NTPLXRHDUXRPNE-UHFFFAOYSA-N 0.000 claims description 26
239000011734 sodium Substances 0.000 claims description 25
229910052708 sodium Inorganic materials 0.000 claims description 25
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 claims description 24
125000000217 alkyl group Chemical group 0.000 claims description 21
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 21
ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 claims description 20
RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 claims description 18
239000002245 particle Substances 0.000 claims description 18
ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 claims description 16
239000000463 material Substances 0.000 claims description 15
QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 claims description 14
229930002839 ionone Natural products 0.000 claims description 13
WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 claims description 12
GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 claims description 12
150000002499 ionone derivatives Chemical class 0.000 claims description 12
FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 claims description 12
235000012141 vanillin Nutrition 0.000 claims description 12
QGFSQVPRCWJZQK-UHFFFAOYSA-N 9-Decen-1-ol Chemical compound OCCCCCCCCC=C QGFSQVPRCWJZQK-UHFFFAOYSA-N 0.000 claims description 11
YPZUZOLGGMJZJO-UHFFFAOYSA-N ambrofix Natural products C1CC2C(C)(C)CCCC2(C)C2C1(C)OCC2 YPZUZOLGGMJZJO-UHFFFAOYSA-N 0.000 claims description 11
YPZUZOLGGMJZJO-LQKXBSAESA-N ambroxan Chemical compound CC([C@@H]1CC2)(C)CCC[C@]1(C)[C@@H]1[C@]2(C)OCC1 YPZUZOLGGMJZJO-LQKXBSAESA-N 0.000 claims description 11
MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 claims description 11
GVONPEQEUQYVNH-SNAWJCMRSA-N 2-Methyl-3-(2-pentenyl)-2-cyclopenten-1-one Chemical compound CC\C=C\CC1=C(C)C(=O)CC1 GVONPEQEUQYVNH-SNAWJCMRSA-N 0.000 claims description 10
239000001725 2-hexylcyclopent-2-en-1-one Substances 0.000 claims description 10
229940062909 amyl salicylate Drugs 0.000 claims description 10
NYNCZOLNVTXTTP-UHFFFAOYSA-N ethyl 2-(1,3-dioxoisoindol-2-yl)acetate Chemical compound C1=CC=C2C(=O)N(CC(=O)OCC)C(=O)C2=C1 NYNCZOLNVTXTTP-UHFFFAOYSA-N 0.000 claims description 10
MDHYEMXUFSJLGV-UHFFFAOYSA-N phenethyl acetate Chemical compound CC(=O)OCCC1=CC=CC=C1 MDHYEMXUFSJLGV-UHFFFAOYSA-N 0.000 claims description 10
229930006727 (-)-endo-fenchol Natural products 0.000 claims description 9
FACFHHMQICTXFZ-UHFFFAOYSA-N 2-(2-phenylimidazo[1,2-a]pyridin-3-yl)ethanamine Chemical compound N1=C2C=CC=CN2C(CCN)=C1C1=CC=CC=C1 FACFHHMQICTXFZ-UHFFFAOYSA-N 0.000 claims description 9
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 9
NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 claims description 9
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 9
239000005770 Eugenol Substances 0.000 claims description 9
IAIHUHQCLTYTSF-MRTMQBJTSA-N Fenchyl alcohol Chemical compound C1C[C@]2(C)[C@H](O)C(C)(C)[C@H]1C2 IAIHUHQCLTYTSF-MRTMQBJTSA-N 0.000 claims description 9
UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 claims description 9
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 9
150000004996 alkyl benzenes Chemical class 0.000 claims description 9
NUQDJSMHGCTKNL-UHFFFAOYSA-N cyclohexyl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1CCCCC1 NUQDJSMHGCTKNL-UHFFFAOYSA-N 0.000 claims description 9
229960002217 eugenol Drugs 0.000 claims description 9
IAIHUHQCLTYTSF-UHFFFAOYSA-N fenchyl alcohol Natural products C1CC2(C)C(O)C(C)(C)C1C2 IAIHUHQCLTYTSF-UHFFFAOYSA-N 0.000 claims description 9
ONKNPOPIGWHAQC-UHFFFAOYSA-N galaxolide Chemical compound C1OCC(C)C2=C1C=C1C(C)(C)C(C)C(C)(C)C1=C2 ONKNPOPIGWHAQC-UHFFFAOYSA-N 0.000 claims description 9
229940067137 musk ketone Drugs 0.000 claims description 9
CZCBTSFUTPZVKJ-UHFFFAOYSA-N rose oxide Chemical compound CC1CCOC(C=C(C)C)C1 CZCBTSFUTPZVKJ-UHFFFAOYSA-N 0.000 claims description 9
229910052938 sodium sulfate Inorganic materials 0.000 claims description 9
235000011152 sodium sulphate Nutrition 0.000 claims description 9
239000004094 surface-active agent Substances 0.000 claims description 9
DGEPZINOUXMMAS-UHFFFAOYSA-N (2,4-dimethylcyclohexyl)methanol Chemical compound CC1CCC(CO)C(C)C1 DGEPZINOUXMMAS-UHFFFAOYSA-N 0.000 claims description 8
KHWTYGFHPHRQMP-UHFFFAOYSA-N (4-propan-2-ylcyclohexyl)methanol Chemical compound CC(C)C1CCC(CO)CC1 KHWTYGFHPHRQMP-UHFFFAOYSA-N 0.000 claims description 8
AZUVBPVDRHGGEP-UHFFFAOYSA-N 6a,9a-dimethyl-4,5,7,8,9,9a-hexahydro-6aH-dipyrrolo(2,3-b;3',2',1'-hi)indole Natural products CC(=C)C1CCC(C)=CCCC(C)=CCCC(C)=CC1O AZUVBPVDRHGGEP-UHFFFAOYSA-N 0.000 claims description 8
WSTYNZDAOAEEKG-UHFFFAOYSA-N Mayol Natural products CC1=C(O)C(=O)C=C2C(CCC3(C4CC(C(CC4(CCC33C)C)=O)C)C)(C)C3=CC=C21 WSTYNZDAOAEEKG-UHFFFAOYSA-N 0.000 claims description 8
229940077388 benzenesulfonate Drugs 0.000 claims description 8
XMWRWTSZNLOZFN-UHFFFAOYSA-N musk xylene Chemical compound CC1=C(N(=O)=O)C(C)=C(N(=O)=O)C(C(C)(C)C)=C1N(=O)=O XMWRWTSZNLOZFN-UHFFFAOYSA-N 0.000 claims description 8
QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 claims description 7
PRNCMAKCNVRZFX-UHFFFAOYSA-N 3,7-dimethyloctan-1-ol Chemical compound CC(C)CCCC(C)CCO PRNCMAKCNVRZFX-UHFFFAOYSA-N 0.000 claims description 7
GPMLJOOQCIHFET-UHFFFAOYSA-N Rhubafuran Chemical compound C1OC(C)CC1(C)C1=CC=CC=C1 GPMLJOOQCIHFET-UHFFFAOYSA-N 0.000 claims description 7
JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 claims description 7
235000000484 citronellol Nutrition 0.000 claims description 7
IMRYETFJNLKUHK-SJCJKPOMSA-N (S,S)-traseolide Chemical compound CC1=C(C(C)=O)C=C2[C@@H](C(C)C)[C@H](C)C(C)(C)C2=C1 IMRYETFJNLKUHK-SJCJKPOMSA-N 0.000 claims description 6
NGYMOTOXXHCHOC-UHFFFAOYSA-N 3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pentan-2-ol Chemical compound CC(O)C(C)CCC1CC=C(C)C1(C)C NGYMOTOXXHCHOC-UHFFFAOYSA-N 0.000 claims description 6
FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 claims description 6
240000002505 Pogostemon cablin Species 0.000 claims description 6
235000011751 Pogostemon cablin Nutrition 0.000 claims description 6
QUMXDOLUJCHOAY-UHFFFAOYSA-N alpha-methylbenzyl acetate Natural products CC(=O)OC(C)C1=CC=CC=C1 QUMXDOLUJCHOAY-UHFFFAOYSA-N 0.000 claims description 6
MIZGSAALSYARKU-UHFFFAOYSA-N cashmeran Chemical compound CC1(C)C(C)C(C)(C)C2=C1C(=O)CCC2 MIZGSAALSYARKU-UHFFFAOYSA-N 0.000 claims description 6
239000010634 clove oil Substances 0.000 claims description 6
229940067107 phenylethyl alcohol Drugs 0.000 claims description 6
OBDUMNZXAIUUTH-UHFFFAOYSA-N tetradec-2-ene Chemical compound CCCCCCCCCCCC=CC OBDUMNZXAIUUTH-UHFFFAOYSA-N 0.000 claims description 6
LFSYLMRHJKGLDV-UHFFFAOYSA-N tetradecanolide Natural products O=C1CCCCCCCCCCCCCO1 LFSYLMRHJKGLDV-UHFFFAOYSA-N 0.000 claims description 6
GFBCBQNBXRPRQD-JLHYYAGUSA-N (2e)-2-benzylidenehexanal Chemical compound CCCC\C(C=O)=C/C1=CC=CC=C1 GFBCBQNBXRPRQD-JLHYYAGUSA-N 0.000 claims description 5
BJLRAKFWOUAROE-UHFFFAOYSA-N 2500-83-6 Chemical compound C12C=CCC2C2CC(OC(=O)C)C1C2 BJLRAKFWOUAROE-UHFFFAOYSA-N 0.000 claims description 5
208000031968 Cadaver Diseases 0.000 claims description 5
241000218645 Cedrus Species 0.000 claims description 5
239000005792 Geraniol Substances 0.000 claims description 5
GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 claims description 5
244000299790 Rheum rhabarbarum Species 0.000 claims description 5
235000009411 Rheum rhabarbarum Nutrition 0.000 claims description 5
125000002947 alkylene group Chemical group 0.000 claims description 5
229940113087 geraniol Drugs 0.000 claims description 5
FJDUDHYHRVPMJZ-UHFFFAOYSA-N nonan-1-amine Chemical compound CCCCCCCCCN FJDUDHYHRVPMJZ-UHFFFAOYSA-N 0.000 claims description 5
NVIPUOMWGQAOIT-UHFFFAOYSA-N (E)-7-Hexadecen-16-olide Natural products O=C1CCCCCC=CCCCCCCCCO1 NVIPUOMWGQAOIT-UHFFFAOYSA-N 0.000 claims description 4
RZXAQFGBENAOAJ-CSKARUKUSA-N (e)-2-methyl-1-(5-methyl-5-bicyclo[2.2.1]hept-2-enyl)pent-1-en-3-ol Chemical compound C1C2C(/C=C(\C)C(O)CC)(C)CC1C=C2 RZXAQFGBENAOAJ-CSKARUKUSA-N 0.000 claims description 4
WSTQLNQRVZNEDV-CSKARUKUSA-N (e)-4-methyldec-3-en-5-ol Chemical compound CCCCCC(O)C(\C)=C\CC WSTQLNQRVZNEDV-CSKARUKUSA-N 0.000 claims description 4
GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 claims description 4
NVIPUOMWGQAOIT-DUXPYHPUSA-N 7-hexadecen-1,16-olide Chemical compound O=C1CCCCC\C=C\CCCCCCCCO1 NVIPUOMWGQAOIT-DUXPYHPUSA-N 0.000 claims description 4
WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 claims description 4
125000003493 decenyl group Chemical group [H]C([*])=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])[H] 0.000 claims description 4
SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 claims description 4
229930007790 rose oxide Natural products 0.000 claims description 4
229940116411 terpineol Drugs 0.000 claims description 4
125000000129 anionic group Chemical group 0.000 claims description 3
KCAZSAYYICOMMG-UHFFFAOYSA-N 6-hydroperoxy-6-oxohexanoic acid Chemical compound OOC(=O)CCCCC(O)=O KCAZSAYYICOMMG-UHFFFAOYSA-N 0.000 claims description 2
UODXCYZDMHPIJE-UHFFFAOYSA-N menthanol Chemical compound CC1CCC(C(C)(C)O)CC1 UODXCYZDMHPIJE-UHFFFAOYSA-N 0.000 claims 4
229910014569 C—OOH Inorganic materials 0.000 claims 2
DNRJTBAOUJJKDY-UHFFFAOYSA-N 2-Acetyl-3,5,5,6,8,8-hexamethyl-5,6,7,8- tetrahydronaphthalene Chemical compound CC(=O)C1=C(C)C=C2C(C)(C)C(C)CC(C)(C)C2=C1 DNRJTBAOUJJKDY-UHFFFAOYSA-N 0.000 claims 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 23
239000008363 phosphate buffer Substances 0.000 description 20
150000004965 peroxy acids Chemical class 0.000 description 13
150000003839 salts Chemical class 0.000 description 12
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 11
239000000243 solution Substances 0.000 description 11
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 9
239000004327 boric acid Substances 0.000 description 9
235000019441 ethanol Nutrition 0.000 description 9
238000005406 washing Methods 0.000 description 9
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
229940022663 acetate Drugs 0.000 description 8
WJJMNDUMQPNECX-UHFFFAOYSA-N dipicolinic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=N1 WJJMNDUMQPNECX-UHFFFAOYSA-N 0.000 description 8
238000000034 method Methods 0.000 description 8
229910052700 potassium Inorganic materials 0.000 description 8
239000011591 potassium Substances 0.000 description 8
239000003795 chemical substances by application Substances 0.000 description 7
239000002253 acid Substances 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
235000014113 dietary fatty acids Nutrition 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
239000000194 fatty acid Substances 0.000 description 6
229930195729 fatty acid Natural products 0.000 description 6
239000000047 product Substances 0.000 description 6
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 6
235000019832 sodium triphosphate Nutrition 0.000 description 6
235000019818 tetrasodium diphosphate Nutrition 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
229910019142 PO4 Inorganic materials 0.000 description 5
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 5
125000001931 aliphatic group Chemical group 0.000 description 5
150000008051 alkyl sulfates Chemical class 0.000 description 5
239000003945 anionic surfactant Substances 0.000 description 5
239000000872 buffer Substances 0.000 description 5
239000007795 chemical reaction product Substances 0.000 description 5
238000004140 cleaning Methods 0.000 description 5
150000004665 fatty acids Chemical class 0.000 description 5
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 5
235000021317 phosphate Nutrition 0.000 description 5
239000003760 tallow Substances 0.000 description 5
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 4
101000581940 Homo sapiens Napsin-A Proteins 0.000 description 4
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
102100027343 Napsin-A Human genes 0.000 description 4
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 4
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235000019864 coconut oil Nutrition 0.000 description 4
239000003240 coconut oil Substances 0.000 description 4
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ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 4
235000019820 disodium diphosphate Nutrition 0.000 description 4
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229940071106 ethylenediaminetetraacetate Drugs 0.000 description 4
QPCDCPDFJACHGM-UHFFFAOYSA-K pentetate(3-) Chemical compound OC(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O QPCDCPDFJACHGM-UHFFFAOYSA-K 0.000 description 4
239000010452 phosphate Substances 0.000 description 4
239000008055 phosphate buffer solution Substances 0.000 description 4
SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 4
239000000344 soap Substances 0.000 description 4
229910000029 sodium carbonate Inorganic materials 0.000 description 4
239000007921 spray Substances 0.000 description 4
RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 3
108090000790 Enzymes Proteins 0.000 description 3
102000004190 Enzymes Human genes 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
108091005804 Peptidases Proteins 0.000 description 3
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 3
239000004353 Polyethylene glycol 8000 Substances 0.000 description 3
102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 3
239000004115 Sodium Silicate Substances 0.000 description 3
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
229910001424 calcium ion Inorganic materials 0.000 description 3
238000001035 drying Methods 0.000 description 3
239000008233 hard water Substances 0.000 description 3
125000002768 hydroxyalkyl group Chemical group 0.000 description 3
239000002736 nonionic surfactant Substances 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 3
235000019446 polyethylene glycol 8000 Nutrition 0.000 description 3
229940085678 polyethylene glycol 8000 Drugs 0.000 description 3
159000000001 potassium salts Chemical class 0.000 description 3
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 3
239000003352 sequestering agent Substances 0.000 description 3
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 3
229910052911 sodium silicate Inorganic materials 0.000 description 3
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238000005507 spraying Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
230000001180 sulfating effect Effects 0.000 description 1
150000003462 sulfoxides Chemical class 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
229940095064 tartrate Drugs 0.000 description 1
RBTVSNLYYIMMKS-UHFFFAOYSA-N tert-butyl 3-aminoazetidine-1-carboxylate;hydrochloride Chemical compound Cl.CC(C)(C)OC(=O)N1CC(N)C1 RBTVSNLYYIMMKS-UHFFFAOYSA-N 0.000 description 1
UIERETOOQGIECD-ONEGZZNKSA-N tiglic acid Chemical compound C\C=C(/C)C(O)=O UIERETOOQGIECD-ONEGZZNKSA-N 0.000 description 1
XMLSXPIVAXONDL-UHFFFAOYSA-N trans-jasmone Natural products CCC=CCC1=C(C)CCC1=O XMLSXPIVAXONDL-UHFFFAOYSA-N 0.000 description 1
229940001496 tribasic sodium phosphate Drugs 0.000 description 1
150000003628 tricarboxylic acids Chemical class 0.000 description 1
229910000406 trisodium phosphate Inorganic materials 0.000 description 1
235000019801 trisodium phosphate Nutrition 0.000 description 1
238000003828 vacuum filtration Methods 0.000 description 1
239000003643 water by type Substances 0.000 description 1
ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 0.000 description 1
239000002888 zwitterionic surfactant Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
- 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)
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)

IE394991A 1990-11-14 1991-11-13 Granular detergent of bleaching compositions containing¹aminoperoxyacid bleach and perfume IE913949A1 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US61342790A	1990-11-14	1990-11-14

Publications (1)

Publication Number	Publication Date
IE913949A1 true IE913949A1 (en)	1992-05-20

Family

ID=24457273

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IE394991A IE913949A1 (en)	1990-11-14	1991-11-13	Granular detergent of bleaching compositions containing¹aminoperoxyacid bleach and perfume

Country Status (17)

Country	Link
EP (1)	EP0557419B1 (fr)
JP (1)	JPH06502669A (fr)
CN (1)	CN1062375A (fr)
AR (1)	AR244802A1 (fr)
AT (1)	ATE133195T1 (fr)
AU (1)	AU9053891A (fr)
BR (1)	BR9106962A (fr)
CA (1)	CA2096254C (fr)
DE (1)	DE69116572T2 (fr)
ES (1)	ES2082445T3 (fr)
IE (1)	IE913949A1 (fr)
MA (1)	MA22338A1 (fr)
MX (1)	MX9102021A (fr)
NZ (1)	NZ240572A (fr)
PT (1)	PT99511A (fr)
TR (1)	TR26092A (fr)
WO (1)	WO1992008780A1 (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5707953A (en) *	1993-04-19	1998-01-13	Akzo Nobel N.V.	Fluidized bed coated amidoperoxyacid bleach composition
US5500154A (en) *	1994-10-20	1996-03-19	The Procter & Gamble Company	Detergent compositions containing enduring perfume
CZ308797A3 (cs) *	1995-04-03	1998-03-18	The Procter & Gamble Company	Bělící přípravky s vybranými parfémy pro maskování zápachu bělidla
EP0778342A1 (fr) *	1995-12-06	1997-06-11	The Procter & Gamble Company	Compositions détergentes
US5780404A (en) *	1996-02-26	1998-07-14	The Procter & Gamble Company	Detergent compositions containing enduring perfume
WO1998056337A1 (fr) *	1997-06-09	1998-12-17	The Procter & Gamble Company	Composition desodorisante contenant du musc et de l'ambre
GB9809772D0 (en) *	1998-05-07	1998-07-08	Quest Int	Perfume composition
EP1072673A3 (fr) *	1999-07-20	2001-03-21	The Procter & Gamble Company	Compositions parfumantes
DE102005054565A1 (de) *	2005-11-14	2007-05-16	Henkel Kgaa	Oxidationsmittel enthaltende,wohlriechende Verbrauchsprodukte

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FI780439A7 (fi) *	1978-01-12	1979-07-13	Unilever Nv	Tvaettmedel
FR2537732A1 (fr) *	1982-12-10	1984-06-15	Thomson Csf	Dispositif d'echauffement d'une zone annulaire superficielle d'un objet filiforme
GB8334159D0 (en) *	1983-12-22	1984-02-01	Unilever Plc	Perfume
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
DE3623619C1 (de) *	1986-07-12	1987-09-10	Ant Nachrichtentech	Verfahren zum Ausrichten zweier Lichtleitfaserenden auf stirnseitigen Kontakt
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
US4727237A (en) *	1987-05-04	1988-02-23	Hewlett-Packard Company	Pyrolysis coated optical fiber splices: apparatus and method
US4909953A (en) *	1988-06-30	1990-03-20	The Procter & Gamble Company	Phosphate buffer wash for improved amidoperoxyacid storage stability
US4932989A (en) *	1989-04-05	1990-06-12	At&T Bell Laboratories	Method and apparatus for fabricating microlenses on optical fibers
GB8914055D0 (en) *	1989-06-19	1989-08-09	Unilever Plc	Low-odour deodorant perfume compositions

1991
- 1991-11-06 AU AU90538/91A patent/AU9053891A/en not_active Abandoned
- 1991-11-06 AT AT92900440T patent/ATE133195T1/de not_active IP Right Cessation
- 1991-11-06 ES ES92900440T patent/ES2082445T3/es not_active Expired - Lifetime
- 1991-11-06 BR BR919106962A patent/BR9106962A/pt unknown
- 1991-11-06 EP EP92900440A patent/EP0557419B1/fr not_active Expired - Lifetime
- 1991-11-06 DE DE69116572T patent/DE69116572T2/de not_active Expired - Fee Related
- 1991-11-06 CA CA002096254A patent/CA2096254C/fr not_active Expired - Fee Related
- 1991-11-06 JP JP4501056A patent/JPH06502669A/ja active Pending
- 1991-11-06 WO PCT/US1991/008206 patent/WO1992008780A1/fr not_active Ceased
- 1991-11-12 MX MX9102021A patent/MX9102021A/es unknown
- 1991-11-13 IE IE394991A patent/IE913949A1/en not_active Application Discontinuation
- 1991-11-13 TR TR91/1071A patent/TR26092A/xx unknown
- 1991-11-13 NZ NZ240572A patent/NZ240572A/en unknown
- 1991-11-13 AR AR91321142A patent/AR244802A1/es active
- 1991-11-13 MA MA22621A patent/MA22338A1/fr unknown
- 1991-11-14 PT PT99511A patent/PT99511A/pt not_active Application Discontinuation
- 1991-11-14 CN CN91111518.8A patent/CN1062375A/zh not_active Withdrawn

Also Published As

Publication number	Publication date
WO1992008780A1 (fr)	1992-05-29
CA2096254A1 (fr)	1992-05-15
EP0557419B1 (fr)	1996-01-17
CA2096254C (fr)	1998-01-06
AU9053891A (en)	1992-06-11
JPH06502669A (ja)	1994-03-24
NZ240572A (en)	1994-12-22
MX9102021A (es)	1994-04-29
AR244802A1 (es)	1993-11-30
CN1062375A (zh)	1992-07-01
ES2082445T3 (es)	1996-03-16
MA22338A1 (fr)	1992-07-01
DE69116572D1 (de)	1996-02-29
BR9106962A (pt)	1993-08-31
ATE133195T1 (de)	1996-02-15
DE69116572T2 (de)	1996-09-19
EP0557419A1 (fr)	1993-09-01
TR26092A (tr)	1994-12-15
PT99511A (pt)	1992-09-30

Legal Events

Date	Code	Title	Description
2002-11-27	FC9A	Application refused sect. 31(1)

Publication	Publication Date	Title
CA2004269C (fr)	1995-02-21	Coloration de produits d'extrusion stabilises contenant des activants d'agent de blanchiment
US5405412A (en)	1995-04-11	Bleaching compounds comprising N-acyl caprolactam and alkanoyloxybenzene sulfonate bleach activators
US5405413A (en)	1995-04-11	Bleaching compounds comprising acyl valerolactam bleach activators
US4412934A (en)	1983-11-01	Bleaching compositions
US4606838A (en)	1986-08-19	Bleaching compositions comprising alkoxy substituted aromatic peroxyacids
EP0699189B1 (fr)	1998-07-29	Composes de blanchiment comprenant des adjuvants de blanchiment a base de benzoyl caprolactame substitue
US4923631A (en)	1990-05-08	Perfume and bleach compositions
US4852989A (en)	1989-08-01	Bleaching compounds and compositions comprising fatty peroxyacids salts thereof and precursors therefor having amide moieties in the fatty chain
US5055218A (en)	1991-10-08	Bleach granules containing an amidoperoxyacid
EP0170386A2 (fr)	1986-02-05	Combinaisons de blanchiment et compositions contenant des acides gras péroxy, leurs sels et précurseurs
US4525292A (en)	1985-06-25	Bleaching detergent compositions comprising sulfosuccinate bleach promoters
EP0557419B1 (fr)	1996-01-17	Compositions granulaires detersives ou de blanchiment contenant un agent de blanchiment d'amidoperoxyacide et un parfum
EP0163331A1 (fr)	1985-12-04	Composition granulaires détergent-agent de blanchiment
CA2162362C (fr)	1999-07-27	Composes de blanchiment renfermant des activateurs de blanchiment a base de caprolactame n-acyle et de sulfonate d'alcanoyloxybenzene
US6034047A (en)	2000-03-07	Bleach detergent compositions comprising nitrones and nitroso spin traps
EP0195597A1 (fr)	1986-09-24	Activateurs de blanchiment et compositions containing them
CA2022321C (fr)	1995-02-14	Compositions detergents granulaires a solubilite amelioree
HK1006465B (en)	1999-02-26	Bleach granules containing an amidoperoxyacid
MXPA00009189A (en)	2001-12-04	Detergent composition containing cylindrically-shaped bleach activator extrudates having enhanced flowability