CZ116595A3 - Dyestuff-transfer inhibiting stable liquid detergents - Google Patents

Dyestuff-transfer inhibiting stable liquid detergents Download PDF

Info

Publication number: CZ116595A3
Authority: CZ; Czechia
Prior art keywords: transfer inhibiting; oxide; polyamine; dye transfer; group
Prior art date: 1992-11-06

Application number

CZ951165A

Other languages

Czech (cs)

English (en)

Inventor

Abdennaceur Fredj

Patrick Willy Goethals

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.)

1992-11-06

Filing date

1993-11-03

Publication date

1995-12-13

1993-11-03 Application filed by Procter & Gamble filed Critical Procter & Gamble

1995-12-13 Publication of CZ116595A3 publication Critical patent/CZ116595A3/cs

Links

230000002401 inhibitory effect Effects 0.000 title claims abstract description 14
239000003599 detergent Substances 0.000 title claims description 26
239000007788 liquid Substances 0.000 title claims description 22
239000000203 mixture Substances 0.000 claims abstract description 35
150000001204 N-oxides Chemical class 0.000 claims abstract description 25
229920000768 polyamine Polymers 0.000 claims abstract description 24
229920000642 polymer Polymers 0.000 claims abstract description 23
125000003118 aryl group Chemical group 0.000 claims abstract description 20
239000003945 anionic surfactant Substances 0.000 claims abstract description 19
239000004094 surface-active agent Substances 0.000 claims description 10
230000002209 hydrophobic effect Effects 0.000 claims description 7
230000003287 optical effect Effects 0.000 claims description 7
102000004190 Enzymes Human genes 0.000 claims description 5
108090000790 Enzymes Proteins 0.000 claims description 5
239000000945 filler Substances 0.000 claims description 5
239000004615 ingredient Substances 0.000 claims description 3
239000000654 additive Substances 0.000 claims 1
230000000996 additive effect Effects 0.000 claims 1
229920002717 polyvinylpyridine Polymers 0.000 claims 1
-1 di-anilinodicyclohexylamine Chemical compound 0.000 description 15
125000000217 alkyl group Chemical group 0.000 description 12
239000000975 dye Substances 0.000 description 12
239000011734 sodium Substances 0.000 description 12
125000004432 carbon atom Chemical group C* 0.000 description 11
229910052708 sodium Inorganic materials 0.000 description 11
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 9
235000014113 dietary fatty acids Nutrition 0.000 description 8
229930195729 fatty acid Natural products 0.000 description 8
239000000194 fatty acid Substances 0.000 description 8
229910052757 nitrogen Inorganic materials 0.000 description 8
150000003839 salts Chemical class 0.000 description 8
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
150000004665 fatty acids Chemical class 0.000 description 7
125000004433 nitrogen atom Chemical group N* 0.000 description 7
239000002253 acid Substances 0.000 description 6
150000008051 alkyl sulfates Chemical class 0.000 description 6
125000000623 heterocyclic group Chemical group 0.000 description 6
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
125000002723 alicyclic group Chemical group 0.000 description 5
125000001931 aliphatic group Chemical group 0.000 description 5
150000001412 amines Chemical class 0.000 description 5
239000003795 chemical substances by application Substances 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
239000000463 material Substances 0.000 description 5
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 4
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
229910052783 alkali metal Inorganic materials 0.000 description 4
239000007844 bleaching agent Substances 0.000 description 4
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 4
235000019864 coconut oil Nutrition 0.000 description 4
239000003240 coconut oil Substances 0.000 description 4
239000002736 nonionic surfactant Substances 0.000 description 4
241000894007 species Species 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 3
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
239000003086 colorant Substances 0.000 description 3
229920001577 copolymer Polymers 0.000 description 3
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 3
239000004744 fabric Substances 0.000 description 3
125000001183 hydrocarbyl group Chemical group 0.000 description 3
229920005646 polycarboxylate Polymers 0.000 description 3
229910052700 potassium Inorganic materials 0.000 description 3
239000011591 potassium Substances 0.000 description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
229920006395 saturated elastomer Polymers 0.000 description 3
150000003467 sulfuric acid derivatives Chemical class 0.000 description 3
239000003760 tallow Substances 0.000 description 3
XMVBHZBLHNOQON-UHFFFAOYSA-N 2-butyl-1-octanol Chemical compound CCCCCCC(CO)CCCC XMVBHZBLHNOQON-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
150000001340 alkali metals Chemical class 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
229910000323 aluminium silicate Inorganic materials 0.000 description 2
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
238000005282 brightening Methods 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
150000001768 cations Chemical class 0.000 description 2
PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
239000003205 fragrance Substances 0.000 description 2
239000008103 glucose Substances 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
239000000178 monomer Substances 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
239000001267 polyvinylpyrrolidone Substances 0.000 description 2
229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
150000003138 primary alcohols Chemical class 0.000 description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
239000000344 soap Substances 0.000 description 2
239000003381 stabilizer Substances 0.000 description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
GHPCICSQWQDZLM-UHFFFAOYSA-N 1-(4-chlorophenyl)sulfonyl-1-methyl-3-propylurea Chemical compound CCCNC(=O)N(C)S(=O)(=O)C1=CC=C(Cl)C=C1 GHPCICSQWQDZLM-UHFFFAOYSA-N 0.000 description 1
OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
QDCPNGVVOWVKJG-VAWYXSNFSA-N 2-[(e)-dodec-1-enyl]butanedioic acid Chemical compound CCCCCCCCCC\C=C\C(C(O)=O)CC(O)=O QDCPNGVVOWVKJG-VAWYXSNFSA-N 0.000 description 1
BPZCDGMBCYAEKM-UHFFFAOYSA-N 2-amino-3-morpholin-4-ylphenol Chemical compound O1CCN(CC1)C=1C(=C(C=CC1)O)N BPZCDGMBCYAEKM-UHFFFAOYSA-N 0.000 description 1
XUKPITDBRGRGFK-UHFFFAOYSA-N 2-benzo[e]benzotriazol-2-yl-6-(2-phenylethenyl)benzenesulfonic acid Chemical compound N=1N(N=C2C1C1=CC=CC=C1C=C2)C2=C(C(=CC=C2)C=CC2=CC=CC=C2)S(=O)(=O)O XUKPITDBRGRGFK-UHFFFAOYSA-N 0.000 description 1
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
MWTDCUHMQIAYDT-UHFFFAOYSA-N 2-tetradecylbutanedioic acid Chemical compound CCCCCCCCCCCCCCC(C(O)=O)CC(O)=O MWTDCUHMQIAYDT-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
GSSXLFACIJSBOM-UHFFFAOYSA-N 2h-pyran-2-ol Chemical compound OC1OC=CC=C1 GSSXLFACIJSBOM-UHFFFAOYSA-N 0.000 description 1
ZTGKHKPZSMMHNM-UHFFFAOYSA-N 3-(2-phenylethenyl)benzene-1,2-disulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC(C=CC=2C=CC=CC=2)=C1S(O)(=O)=O ZTGKHKPZSMMHNM-UHFFFAOYSA-N 0.000 description 1
LWYAUHJRUCQFCX-UHFFFAOYSA-N 4-dodecoxy-4-oxobutanoic acid Chemical compound CCCCCCCCCCCCOC(=O)CCC(O)=O LWYAUHJRUCQFCX-UHFFFAOYSA-N 0.000 description 1
VCDRAONLIPOEFL-UHFFFAOYSA-N 4-n-[4-(4-anilinoanilino)phenyl]benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NC(C=C1)=CC=C1NC(C=C1)=CC=C1NC1=CC=CC=C1 VCDRAONLIPOEFL-UHFFFAOYSA-N 0.000 description 1
XDJAHNALPHLVAX-UHFFFAOYSA-N 4-oxo-4-tetradec-2-enoxybutanoic acid Chemical compound CCCCCCCCCCCC=CCOC(=O)CCC(O)=O XDJAHNALPHLVAX-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
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 1
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 1
125000000815 N-oxide group Chemical group 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004642 Polyimide Substances 0.000 description 1
229910004298 SiO 2 Inorganic materials 0.000 description 1
239000004115 Sodium Silicate Substances 0.000 description 1
JCQLAAMILSTQJX-UHFFFAOYSA-L [Na+].[Na+].C1(=C(C(=CC=C1)S(=O)(=O)[O-])S(=O)(=O)[O-])C=CC1=CC=CC=C1 Chemical compound [Na+].[Na+].C1(=C(C(=CC=C1)S(=O)(=O)[O-])S(=O)(=O)[O-])C=CC1=CC=CC=C1 JCQLAAMILSTQJX-UHFFFAOYSA-L 0.000 description 1
239000012190 activator Substances 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
125000005210 alkyl ammonium group Chemical group 0.000 description 1
125000005192 alkyl ethylene group Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
239000004327 boric acid Substances 0.000 description 1
PDNMJCUSNRJCAK-UHFFFAOYSA-N butanedioic acid dodec-2-ene Chemical compound CC=CCCCCCCCCC.C(CCC(=O)O)(=O)O PDNMJCUSNRJCAK-UHFFFAOYSA-N 0.000 description 1
HXDRSFFFXJISME-UHFFFAOYSA-N butanedioic acid;2,3-dihydroxybutanedioic acid Chemical compound OC(=O)CCC(O)=O.OC(=O)C(O)C(O)C(O)=O HXDRSFFFXJISME-UHFFFAOYSA-N 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
125000004185 ester group Chemical group 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
UZABCLFSICXBCM-UHFFFAOYSA-N ethoxy hydrogen sulfate Chemical class CCOOS(O)(=O)=O UZABCLFSICXBCM-UHFFFAOYSA-N 0.000 description 1
238000007046 ethoxylation reaction Methods 0.000 description 1
XWEOGMYZFCHQNT-UHFFFAOYSA-N ethyl 2-(2-methyl-1,3-dioxolan-2-yl)acetate Chemical compound CCOC(=O)CC1(C)OCCO1 XWEOGMYZFCHQNT-UHFFFAOYSA-N 0.000 description 1
229940071106 ethylenediaminetetraacetate Drugs 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
238000009472 formulation Methods 0.000 description 1
125000005456 glyceride group Chemical group 0.000 description 1
150000002391 heterocyclic compounds Chemical class 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
125000001165 hydrophobic group Chemical group 0.000 description 1
238000005342 ion exchange Methods 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
239000008101 lactose Substances 0.000 description 1
239000012669 liquid formulation Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
238000005259 measurement Methods 0.000 description 1
229910021645 metal ion Inorganic materials 0.000 description 1
238000000034 method Methods 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
125000001741 organic sulfur group Chemical group 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920001281 polyalkylene Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001721 polyimide Polymers 0.000 description 1
159000000001 potassium salts Chemical class 0.000 description 1
239000000047 product Substances 0.000 description 1
ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
229920005604 random copolymer Polymers 0.000 description 1
238000006268 reductive amination reaction Methods 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
239000002689 soil Substances 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
238000010186 staining Methods 0.000 description 1
150000003443 succinic acid derivatives Chemical class 0.000 description 1
235000000346 sugar Nutrition 0.000 description 1
150000008163 sugars Chemical class 0.000 description 1
230000001180 sulfating effect Effects 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
150000003457 sulfones Chemical group 0.000 description 1
229910021653 sulphate ion Inorganic materials 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229940095064 tartrate Drugs 0.000 description 1
KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
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 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
239000010457 zeolite 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/40—Dyes ; Pigments
- C11D3/42—Brightening agents ; Blueing agents
- 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
- 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0021—Dye-stain or dye-transfer inhibiting 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3792—Amine oxide containing polymers
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/525—Carboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain two or more hydroxy groups per alkyl group, e.g. R3 being a reducing sugar rest

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)
Detergent Compositions (AREA)
Cosmetics (AREA)

CZ951165A 1992-11-06 1993-11-03 Dyestuff-transfer inhibiting stable liquid detergents CZ116595A3 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP92870182A EP0596185A1 (fr)	1992-11-06	1992-11-06	Détergents liquides stables inhibant le transfert de couleur

Publications (1)

Publication Number	Publication Date
CZ116595A3 true CZ116595A3 (en)	1995-12-13

Family

ID=8212282

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CZ951165A CZ116595A3 (en)	1992-11-06	1993-11-03	Dyestuff-transfer inhibiting stable liquid detergents

Country Status (11)

Country	Link
EP (1)	EP0596185A1 (fr)
JP (1)	JPH08503246A (fr)
KR (1)	KR950704458A (fr)
CN (1)	CN1041840C (fr)
AU (1)	AU670851B2 (fr)
CA (1)	CA2148808C (fr)
CZ (1)	CZ116595A3 (fr)
HU (1)	HUT71963A (fr)
MX (1)	MX9306971A (fr)
PL (1)	PL175677B1 (fr)
WO (1)	WO1994011473A1 (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5597795A (en) *	1992-10-27	1997-01-28	The Procter & Gamble Company	Detergent compositions inhibiting dye transfer
CN1145093A (zh) *	1994-03-30	1997-03-12	普罗格特-甘布尔公司	具有改进的增白和染料转移抑制效果的洗衣用洗涤剂条
US5804543A (en) *	1994-10-11	1998-09-08	The Procter & Gamble Company	Detergent compositions with optimized surfactant systems to provide dye transfer inhibition benefits
DE69706715T2 (de)	1996-01-25	2002-05-29	Unilever N.V., Rotterdam	Waschmittelzusammensetzung
DE10353310A1 (de) *	2003-11-10	2005-06-09	Maier, Ursula, Dipl.-Ing.	Verwendung einer Lösung mit mindestens einem nichtionischen Tensid
DE102007037430A1 (de) *	2007-08-08	2009-02-12	Henkel Ag & Co. Kgaa	Farbschützendes Wasch- oder Reinigungsmittel mit optischem Aufheller
JP5396707B2 (ja) *	2007-11-07	2014-01-22	ライオンハイジーン株式会社	洗浄剤組成物
EP2964740B1 (fr) *	2013-03-05	2017-10-04	The Procter and Gamble Company	Compositions comprenat des combinaisons de tensio-actifs dérivés d'amides de sucres
DE102013205079A1 (de) *	2013-03-22	2014-09-25	Henkel Ag & Co. Kgaa	Farbschützendes Wasch- oder Reinigungsmittel mit optischem Aufheller
JP2017509774A (ja)	2014-01-20	2017-04-06	ザプロクターアンドギャンブルカンパニー	蛍光増白剤プレミックス
CN105907490A (zh) *	2016-05-17	2016-08-31	河南工程学院	一种酸性护色洗涤剂组合物

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3637339A (en) *	1968-03-07	1972-01-25	Frederick William Gray	Stain removal
BE785653A (fr) *	1971-07-02	1973-01-02	Procter & Gamble Europ
US4123376A (en) *	1973-08-24	1978-10-31	Colgate-Palmolive Company	Peroxymonosulfate-base bleaching and bleaching detergent compositions
US4300897A (en) *	1973-08-24	1981-11-17	Colgate-Palmolive Company	Method for bleaching with peroxymonosulfate-based compositions
US3929678A (en) *	1974-08-01	1975-12-30	Procter & Gamble	Detergent composition having enhanced particulate soil removal performance
DE2504276A1 (de) *	1975-02-01	1976-08-05	Henkel & Cie Gmbh	Waschmittel mit einem gehalt an n-alkansulfonaten und optischen aufhellern
US4146496A (en) *	1977-05-18	1979-03-27	Colgate-Palmolive Company	Peroxy bleach system suitable for colored laundry
DE2814329A1 (de) *	1978-04-03	1979-10-11	Henkel Kgaa	Waschmittel mit einem gehalt an verfaerbungsinhibierenden zusaetzen
US4545919A (en) *	1982-08-31	1985-10-08	Ciba-Geigy Corporation	Detergent composition for washing off dyeings obtained with fibre-reactive dyes and washing process comprising the use thereof
US4548744A (en) *	1983-07-22	1985-10-22	Connor Daniel S	Ethoxylated amine oxides having clay soil removal/anti-redeposition properties useful in detergent compositions
DE3585512D1 (de) *	1984-12-28	1992-04-09	Procter & Gamble	Fluessiges hypochlorit-bleichmittel, enthaltend optische aufheller, geloest in aminoxid.
EP0314630A3 (fr) *	1987-10-30	1989-10-25	Sandoz Ag	Compositions détergentes
EP0350449A3 (fr) *	1988-07-08	1990-10-24	Ciba-Geigy Ag	Composition détergente liquide contenant des azurants optiques

1992
- 1992-11-06 EP EP92870182A patent/EP0596185A1/fr not_active Withdrawn
1993
- 1993-11-03 PL PL93308760A patent/PL175677B1/pl unknown
- 1993-11-03 WO PCT/US1993/010542 patent/WO1994011473A1/fr not_active Ceased
- 1993-11-03 CA CA002148808A patent/CA2148808C/fr not_active Expired - Fee Related
- 1993-11-03 JP JP6512172A patent/JPH08503246A/ja active Pending
- 1993-11-03 AU AU55904/94A patent/AU670851B2/en not_active Ceased
- 1993-11-03 CZ CZ951165A patent/CZ116595A3/cs unknown
- 1993-11-03 KR KR1019950701775A patent/KR950704458A/ko not_active Withdrawn
- 1993-11-03 HU HU9501296A patent/HUT71963A/hu unknown
- 1993-11-06 CN CN93112697A patent/CN1041840C/zh not_active Expired - Fee Related
- 1993-11-08 MX MX9306971A patent/MX9306971A/es not_active IP Right Cessation

Also Published As

Publication number	Publication date
CA2148808C (fr)	1999-05-18
KR950704458A (ko)	1995-11-20
PL175677B1 (pl)	1999-01-29
EP0596185A1 (fr)	1994-05-11
PL308760A1 (en)	1995-08-21
AU670851B2 (en)	1996-08-01
CN1041840C (zh)	1999-01-27
CN1088610A (zh)	1994-06-29
CA2148808A1 (fr)	1994-05-26
JPH08503246A (ja)	1996-04-09
AU5590494A (en)	1994-06-08
WO1994011473A1 (fr)	1994-05-26
HU9501296D0 (en)	1995-06-28
MX9306971A (es)	1995-01-31
HUT71963A (en)	1996-02-28

Publication	Publication Date	Title
CA1141108A (fr)	1983-02-15	Compositions detergentes-assouplissantes
US4233167A (en)	1980-11-11	Liquid detergent softening and brightening composition
AU661672B2 (en)	1995-08-03	Detergent compositions containing lipase and water-soluble quaternary ammonium compounds
US5466802A (en)	1995-11-14	Detergent compositions which provide dye transfer inhibition benefits
US5035814A (en)	1991-07-30	Liquid detergent having improved softening properties
US5783548A (en)	1998-07-21	Stable liquid detergent compositions inhibiting dye transfer
CA1231205A (fr)	1988-01-12	Detergents liquides stables aux agents tensioactifs anioniques et aux agents d'avivage monosulfones
AU595851B2 (en)	1990-04-12	Liquid softergent having improved detergency containing alkyl glycoside
AU600694B2 (en)	1990-08-23	Liquid detergent having improved softening properties
CZ116595A3 (en)	1995-12-13	Dyestuff-transfer inhibiting stable liquid detergents
CA2006439A1 (fr)	1990-07-03	Detersif non ionique pour la lessive
KR950004931B1 (ko)	1995-05-16	소수성 증백제를 함유하는 액체 세제 조성물
EP0672099B1 (fr)	1997-04-02	Compositions de detergents liquides stables inhibant le transfert des couleurs
WO1995003390A1 (fr)	1995-02-02	Compositions detergentes inhibant le transfert de colorants en cours de lavage
JPH09507527A (ja)	1997-07-29	布帛斑点形成を防止するための増白剤含有液体洗剤組成物中における重合体の用途
US4970029A (en)	1990-11-13	Stable liquid detergent containing anionic surfactant and monosulfonated brightener
CA1315638C (fr)	1993-04-06	Formules de detergent doux liquide a caracteristique de haute stabilite et adoucissante
US20090293210A1 (en)	2009-12-03	Laundering process for whitening synthetic textiles
US5151223A (en)	1992-09-29	Liquid softergent formulations having improved stability and softening properties
US4978475A (en)	1990-12-18	Stable liquid detergents containing anionic surfactant and monosulfonated brightener
HU217365B (hu)	2000-01-28	Festékátvitelt gátló készítmény és ezt tartalmazó mosószer
US5597795A (en)	1997-01-28	Detergent compositions inhibiting dye transfer
CA1235553A (fr)	1988-04-26	Detergents liquides stables a teneur d'agent tensio-actif anionique et agent d'avivage monosulfone
US5024786A (en)	1991-06-18	Detergent compositions containing an anionic surfactant and a 4,4'-bis(triazinylamino)-stilbene disulphonic acid optical brightener
US5604194A (en)	1997-02-18	Stable liquid detergent compositions comprising specific brightener and PVP to inhibit dye transfer