IL112069A - Preparations for the treatment of textiles containing compounds for ultraviolet light absorption - Google Patents

Preparations for the treatment of textiles containing compounds for ultraviolet light absorption

Info

Publication number: IL112069A
Authority: IL; Israel
Prior art keywords: composition according; composition; hydrogen; formula; triazine
Prior art date: 1993-12-23

Application number

IL112069A

Other languages

English (en)

Hebrew (he)

Other versions

IL112069A0 (en

Original Assignee

Ciba Geigy Ag

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.)

1993-12-23

Filing date

1994-12-20

Publication date

1998-04-05

1994-12-20 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1995-03-15 Publication of IL112069A0 publication Critical patent/IL112069A0/xx

1998-04-05 Publication of IL112069A publication Critical patent/IL112069A/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 107
239000004753 textile Substances 0.000 title claims abstract description 40
150000001875 compounds Chemical class 0.000 title claims description 40
239000006096 absorbing agent Substances 0.000 claims abstract description 59
239000004744 fabric Substances 0.000 claims abstract description 34
238000000034 method Methods 0.000 claims abstract description 19
239000004615 ingredient Substances 0.000 claims abstract description 17
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 15
125000002091 cationic group Chemical group 0.000 claims abstract description 13
239000002979 fabric softener Substances 0.000 claims abstract description 13
YHCGGLXPGFJNCO-UHFFFAOYSA-N 2-(2H-benzotriazol-4-yl)phenol Chemical compound OC1=CC=CC=C1C1=CC=CC2=C1N=NN2 YHCGGLXPGFJNCO-UHFFFAOYSA-N 0.000 claims abstract description 11
239000004902 Softening Agent Substances 0.000 claims abstract description 9
-1 phosphate anion Chemical group 0.000 claims description 64
229910052739 hydrogen Inorganic materials 0.000 claims description 55
239000001257 hydrogen Substances 0.000 claims description 54
150000002431 hydrogen Chemical group 0.000 claims description 25
239000006081 fluorescent whitening agent Substances 0.000 claims description 21
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 20
FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 claims description 19
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 18
229910052736 halogen Inorganic materials 0.000 claims description 17
150000002367 halogens Chemical class 0.000 claims description 17
229910052757 nitrogen Inorganic materials 0.000 claims description 17
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 14
125000004433 nitrogen atom Chemical group N* 0.000 claims description 12
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 11
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical group O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 claims description 9
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 9
125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims description 8
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 8
150000001450 anions Chemical group 0.000 claims description 8
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical group [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 7
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 7
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
239000011734 sodium Chemical group 0.000 claims description 7
229910052708 sodium Inorganic materials 0.000 claims description 7
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 6
239000002671 adjuvant Substances 0.000 claims description 6
239000000460 chlorine Substances 0.000 claims description 6
229910052801 chlorine Inorganic materials 0.000 claims description 6
150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 6
150000003254 radicals Chemical group 0.000 claims description 6
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
239000011575 calcium Chemical group 0.000 claims description 5
229910052791 calcium Inorganic materials 0.000 claims description 5
239000011777 magnesium Chemical group 0.000 claims description 5
229910052749 magnesium Inorganic materials 0.000 claims description 5
229910052700 potassium Inorganic materials 0.000 claims description 5
150000003852 triazoles Chemical class 0.000 claims description 5
210000002268 wool Anatomy 0.000 claims description 5
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical group [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 4
229920000742 Cotton Polymers 0.000 claims description 4
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical group [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 4
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
239000000975 dye Substances 0.000 claims description 4
239000011591 potassium Chemical group 0.000 claims description 4
125000001424 substituent group Chemical group 0.000 claims description 4
239000003760 tallow Substances 0.000 claims description 4
BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical group CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 claims description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 3
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical group [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 3
239000004952 Polyamide Substances 0.000 claims description 3
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical group I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 3
229920002647 polyamide Polymers 0.000 claims description 3
229920000728 polyester Polymers 0.000 claims description 3
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 3
LSXNXAWTJRVPSK-UHFFFAOYSA-M 2-(2-heptadec-1-enyl-1-octadecyl-4,5-dihydroimidazol-1-ium-1-yl)ethanol;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+]1(CCO)CCN=C1C=CCCCCCCCCCCCCCCC LSXNXAWTJRVPSK-UHFFFAOYSA-M 0.000 claims description 2
QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 claims description 2
RUCYXNQCSQDELI-UHFFFAOYSA-J C(CCCCCCCCCCCCCCCCC)[N+](C)(C)CCCCCCCCCCCCCCCCCC.[Br-].C(CCCCCCCCCCCCCCCCC)[N+](C)(C)CCCCCCCCCCCCCCCCCC.[Cl-].C(CCCCCCCCCCCCCCC)[N+](C)(C)CCCCCCCCCCCCCCCC.[Cl-].C(CCCCCCCCCCC)[N+](C)(C)CCCCCCCCCCCC.[Cl-].C(CCCCCCCCCCCCCCCCC)[N+](C)(C)CCCCCCCCCCCCCCCCCC Chemical compound C(CCCCCCCCCCCCCCCCC)[N+](C)(C)CCCCCCCCCCCCCCCCCC.[Br-].C(CCCCCCCCCCCCCCCCC)[N+](C)(C)CCCCCCCCCCCCCCCCCC.[Cl-].C(CCCCCCCCCCCCCCC)[N+](C)(C)CCCCCCCCCCCCCCCC.[Cl-].C(CCCCCCCCCCC)[N+](C)(C)CCCCCCCCCCCC.[Cl-].C(CCCCCCCCCCCCCCCCC)[N+](C)(C)CCCCCCCCCCCCCCCCCC RUCYXNQCSQDELI-UHFFFAOYSA-J 0.000 claims description 2
KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical group [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 2
229910002651 NO3 Inorganic materials 0.000 claims description 2
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical group [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 2
IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical group [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 claims description 2
229910019142 PO4 Inorganic materials 0.000 claims description 2
239000007983 Tris buffer Substances 0.000 claims description 2
CDBJBDCGBLHNGX-UHFFFAOYSA-M [Cl-].C(=CCCCCCCCCCCCCCCC)C=1[N+](CCN1)(CC1=CC=CC=C1)CCO Chemical compound [Cl-].C(=CCCCCCCCCCCCCCCC)C=1[N+](CCN1)(CC1=CC=CC=C1)CCO CDBJBDCGBLHNGX-UHFFFAOYSA-M 0.000 claims description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 claims description 2
230000000844 anti-bacterial effect Effects 0.000 claims description 2
239000003899 bactericide agent Substances 0.000 claims description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 2
238000004040 coloring Methods 0.000 claims description 2
230000007797 corrosion Effects 0.000 claims description 2
238000005260 corrosion Methods 0.000 claims description 2
239000003995 emulsifying agent Substances 0.000 claims description 2
239000003349 gelling agent Substances 0.000 claims description 2
239000003112 inhibitor Substances 0.000 claims description 2
239000002736 nonionic surfactant Substances 0.000 claims description 2
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 2
229940049964 oleate Drugs 0.000 claims description 2
239000003605 opacifier Substances 0.000 claims description 2
239000002304 perfume Substances 0.000 claims description 2
239000010452 phosphate Substances 0.000 claims description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 claims description 2
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims 4
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims 1
239000004665 cationic fabric softener Substances 0.000 claims 1
150000001805 chlorine compounds Chemical group 0.000 claims 1
125000002636 imidazolinyl group Chemical group 0.000 claims 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
125000001425 triazolyl group Chemical group 0.000 claims 1
239000003795 chemical substances by application Substances 0.000 abstract description 3
238000004078 waterproofing Methods 0.000 abstract description 3
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 27
WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Natural products O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 20
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 18
210000003491 skin Anatomy 0.000 description 16
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 10
125000004093 cyano group Chemical group *C#N 0.000 description 9
239000002253 acid Substances 0.000 description 8
239000007859 condensation product Substances 0.000 description 7
238000004519 manufacturing process Methods 0.000 description 7
230000005855 radiation Effects 0.000 description 7
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 6
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 6
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical group C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 5
239000000835 fiber Substances 0.000 description 5
229910052760 oxygen Inorganic materials 0.000 description 5
239000001301 oxygen Substances 0.000 description 5
229910052717 sulfur Inorganic materials 0.000 description 5
238000005406 washing Methods 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
125000000129 anionic group Chemical group 0.000 description 4
125000000068 chlorophenyl group Chemical group 0.000 description 4
230000006378 damage Effects 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
239000000463 material Substances 0.000 description 4
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
239000011593 sulfur Substances 0.000 description 4
125000003944 tolyl group Chemical group 0.000 description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
239000002585 base Substances 0.000 description 3
229940076810 beta sitosterol Drugs 0.000 description 3
LGJMUZUPVCAVPU-UHFFFAOYSA-N beta-Sitostanol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(CC)C(C)C)C1(C)CC2 LGJMUZUPVCAVPU-UHFFFAOYSA-N 0.000 description 3
NJKOMDUNNDKEAI-UHFFFAOYSA-N beta-sitosterol Natural products CCC(CCC(C)C1CCC2(C)C3CC=C4CC(O)CCC4C3CCC12C)C(C)C NJKOMDUNNDKEAI-UHFFFAOYSA-N 0.000 description 3
238000006243 chemical reaction Methods 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
150000002191 fatty alcohols Chemical class 0.000 description 3
KZJWDPNRJALLNS-VJSFXXLFSA-N sitosterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CC[C@@H](CC)C(C)C)[C@@]1(C)CC2 KZJWDPNRJALLNS-VJSFXXLFSA-N 0.000 description 3
229950005143 sitosterol Drugs 0.000 description 3
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 3
230000037072 sun protection Effects 0.000 description 3
150000003918 triazines Chemical class 0.000 description 3
125000006656 (C2-C4) alkenyl group Chemical group 0.000 description 2
125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
206010042496 Sunburn Diseases 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
125000001309 chloro group Chemical group Cl* 0.000 description 2
238000005520 cutting process Methods 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
238000009472 formulation Methods 0.000 description 2
150000002462 imidazolines Chemical class 0.000 description 2
230000002452 interceptive effect Effects 0.000 description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
229920005610 lignin Polymers 0.000 description 2
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 2
239000000047 product Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
230000037380 skin damage Effects 0.000 description 2
235000011121 sodium hydroxide Nutrition 0.000 description 2
VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
239000000243 solution Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 2
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 1
125000004642 (C1-C12) alkoxy group Chemical group 0.000 description 1
ZPFAVCIQZKRBGF-UHFFFAOYSA-N 1,3,2-dioxathiolane 2,2-dioxide Chemical compound O=S1(=O)OCCO1 ZPFAVCIQZKRBGF-UHFFFAOYSA-N 0.000 description 1
ATZAUOICJHZAFI-UHFFFAOYSA-N 1-(2-phenylphenyl)dibenzofuran Chemical group C1=CC=CC=C1C1=CC=CC=C1C1=CC=CC2=C1C1=CC=CC=C1O2 ATZAUOICJHZAFI-UHFFFAOYSA-N 0.000 description 1
ZMLPKJYZRQZLDA-PHEQNACWSA-N 1-[(e)-2-phenylethenyl]-4-[4-[(e)-2-phenylethenyl]phenyl]benzene Chemical group C=1C=CC=CC=1/C=C/C(C=C1)=CC=C1C(C=C1)=CC=C1\C=C\C1=CC=CC=C1 ZMLPKJYZRQZLDA-PHEQNACWSA-N 0.000 description 1
TZXKVJQBBGEMSF-UHFFFAOYSA-N 1-ethenyl-4-[2-(4-ethenylphenyl)ethenyl]benzene Chemical compound C1=CC(C=C)=CC=C1C=CC1=CC=C(C=C)C=C1 TZXKVJQBBGEMSF-UHFFFAOYSA-N 0.000 description 1
JKTAIYGNOFSMCE-UHFFFAOYSA-N 2,3-di(nonyl)phenol Chemical compound CCCCCCCCCC1=CC=CC(O)=C1CCCCCCCCC JKTAIYGNOFSMCE-UHFFFAOYSA-N 0.000 description 1
BIEFDNUEROKZRA-UHFFFAOYSA-N 2-(2-phenylethenyl)aniline Chemical compound NC1=CC=CC=C1C=CC1=CC=CC=C1 BIEFDNUEROKZRA-UHFFFAOYSA-N 0.000 description 1
125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
ISCOWSBMWSYRMK-UHFFFAOYSA-N 2-hydroxy-3-[3-hydroxy-4-[4-[2-hydroxy-4-(2-hydroxy-3-sulfopropoxy)phenyl]-6-phenyl-1,3,5-triazin-2-yl]phenoxy]propane-1-sulfonic acid Chemical compound OC(COc1ccc(c(O)c1)-c1nc(nc(n1)-c1ccc(OCC(O)CS(O)(=O)=O)cc1O)-c1ccccc1)CS(O)(=O)=O ISCOWSBMWSYRMK-UHFFFAOYSA-N 0.000 description 1
FYIXKWULFOCEQD-UHFFFAOYSA-N 3-[4-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-3-hydroxyphenoxy]-2-hydroxypropane-1-sulfonic acid Chemical compound Cc1ccc(c(C)c1)-c1nc(nc(n1)-c1ccc(OCC(O)CS(O)(=O)=O)cc1O)-c1ccc(C)cc1C FYIXKWULFOCEQD-UHFFFAOYSA-N 0.000 description 1
ZENQAFUZFAZRHD-UHFFFAOYSA-N 3-[4-[4,6-bis(4-methylphenyl)-1,3,5-triazin-2-yl]-3-hydroxyphenoxy]-2-hydroxypropane-1-sulfonic acid Chemical compound Cc1ccc(cc1)-c1nc(nc(n1)-c1ccc(OCC(O)CS(O)(=O)=O)cc1O)-c1ccc(C)cc1 ZENQAFUZFAZRHD-UHFFFAOYSA-N 0.000 description 1
SUFVBWNLZKCJOQ-UHFFFAOYSA-N 4-benzoyl-3-hydroxybenzonitrile Chemical compound OC1=CC(C#N)=CC=C1C(=O)C1=CC=CC=C1 SUFVBWNLZKCJOQ-UHFFFAOYSA-N 0.000 description 1
ZOUTYVWHWSUKPL-NOZJJQNGSA-N C[C@H](CS)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(O)=O Chemical group C[C@H](CS)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(O)=O ZOUTYVWHWSUKPL-NOZJJQNGSA-N 0.000 description 1
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
201000009030 Carcinoma Diseases 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Chemical group CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
206010015150 Erythema Diseases 0.000 description 1
206010016275 Fear Diseases 0.000 description 1
BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
206010040799 Skin atrophy Diseases 0.000 description 1
239000004115 Sodium Silicate Substances 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
239000000654 additive Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
125000002947 alkylene group Chemical class 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
125000001204 arachidyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000000732 arylene group Chemical group 0.000 description 1
SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 1
229940077388 benzenesulfonate Drugs 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-M benzoate Chemical compound [O-]C(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-M 0.000 description 1
239000001110 calcium chloride Substances 0.000 description 1
229910001628 calcium chloride Inorganic materials 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 1
150000001896 cresols Chemical class 0.000 description 1
230000000254 damaging effect Effects 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
OGQYPPBGSLZBEG-UHFFFAOYSA-N dimethyl(dioctadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC OGQYPPBGSLZBEG-UHFFFAOYSA-N 0.000 description 1
IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
RSHVNDLJRRLWEF-UHFFFAOYSA-M dioctadecyl-di(propan-2-yl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C(C)C)(C(C)C)CCCCCCCCCCCCCCCCCC RSHVNDLJRRLWEF-UHFFFAOYSA-M 0.000 description 1
239000004664 distearyldimethylammonium chloride (DHTDMAC) Substances 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
210000002615 epidermis Anatomy 0.000 description 1
231100000321 erythema Toxicity 0.000 description 1
125000004705 ethylthio group Chemical group C(C)S* 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002193 fatty amides Chemical class 0.000 description 1
125000001188 haloalkyl group Chemical group 0.000 description 1
238000005259 measurement Methods 0.000 description 1
201000001441 melanoma Diseases 0.000 description 1
125000001802 myricyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
150000002823 nitrates Chemical class 0.000 description 1
150000002826 nitrites Chemical class 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000002245 particle Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical class O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
231100000760 phototoxic Toxicity 0.000 description 1
150000007519 polyprotic acids Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
DOKHEARVIDLSFF-UHFFFAOYSA-N prop-1-en-1-ol Chemical group CC=CO DOKHEARVIDLSFF-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
230000037307 sensitive skin Effects 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
239000004317 sodium nitrate Substances 0.000 description 1
235000010344 sodium nitrate Nutrition 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
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
239000000516 sunscreening agent Substances 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
239000004758 synthetic textile Substances 0.000 description 1
125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229960004418 trolamine Drugs 0.000 description 1
230000037303 wrinkles Effects 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
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/06—Phosphates, including polyphosphates
- C11D3/065—Phosphates, including polyphosphates in admixture with sulfonated products
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/35—Heterocyclic compounds
- D06M13/352—Heterocyclic compounds having five-membered heterocyclic rings
- 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
- C11D1/62—Quaternary ammonium compounds
- 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
- C11D3/001—Softening compositions
- C11D3/0015—Softening compositions liquid
- 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
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/35—Heterocyclic compounds
- D06M13/355—Heterocyclic compounds having six-membered heterocyclic rings
- D06M13/358—Triazines

Landscapes

Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Textile Engineering (AREA)
Inorganic Chemistry (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Detergent Compositions (AREA)

IL112069A 1993-12-23 1994-12-20 Preparations for the treatment of textiles containing compounds for ultraviolet light absorption IL112069A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB939326358A GB9326358D0 (en)	1993-12-23	1993-12-23	Compositions for the treatment of textiles

Publications (2)

Publication Number	Publication Date
IL112069A0 IL112069A0 (en)	1995-03-15
IL112069A true IL112069A (en)	1998-04-05

Family

ID=10747143

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL112069A IL112069A (en)	1993-12-23	1994-12-20	Preparations for the treatment of textiles containing compounds for ultraviolet light absorption

Country Status (13)

Country	Link
US (2)	US6174854B1 (de)
EP (1)	EP0659877B1 (de)
JP (1)	JP3871720B2 (de)
KR (1)	KR100390226B1 (de)
AT (1)	ATE242307T1 (de)
AU (1)	AU684116B2 (de)
BR (1)	BR9405213A (de)
DE (1)	DE69432783T2 (de)
ES (1)	ES2199951T3 (de)
GB (2)	GB9326358D0 (de)
IL (1)	IL112069A (de)
NZ (1)	NZ270206A (de)
ZA (1)	ZA9410243B (de)

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GB9610865D0 (en) *	1996-05-23	1996-07-31	Unilever Plc	Detergent composition
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GB2332444A (en) *	1997-12-20	1999-06-23	Procter & Gamble	A cleaning composition
GB2332443A (en) *	1997-12-20	1999-06-23	Procter & Gamble	Liquid cleaning composition
GB2332445A (en) *	1997-12-20	1999-06-23	Procter & Gamble	Solid detergent compositions
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AU2007214600A1 (en) *	2006-02-14	2007-08-23	Basf Se	Aromatic sulphonate flame retardant compositions
ES2463674T3 (es)	2009-01-19	2014-05-28	Basf Se	Pigmentos negros orgánicos y su preparación
KR101517039B1 (ko) *	2013-12-12	2015-05-04	한국화학연구원	디에스테르기 함유 디암모늄 양이온 계면활성제, 이의 제조방법 및 이를 포함하는 섬유유연제 조성물
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US5474691A (en) *	1994-07-26	1995-12-12	The Procter & Gamble Company	Dryer-added fabric treatment article of manufacture containing antioxidant and sunscreen compounds for sun fade protection of fabrics
ES2152413T3 (es) *	1994-07-26	2001-02-01	Procter & Gamble	Composiciones suavizantes de tejidos con aclarado que contienen antioxidantes para proteccion de tejidos frente a la decoloracion.
CA2192802C (en) *	1994-07-26	2000-11-21	Mark Robert Sivik	Rinse added fabric softener compositions containing sunscreens for sun-fade protection for fabrics

1993
- 1993-12-23 GB GB939326358A patent/GB9326358D0/en active Pending
1994
- 1994-12-14 ES ES94810726T patent/ES2199951T3/es not_active Expired - Lifetime
- 1994-12-14 AT AT94810726T patent/ATE242307T1/de not_active IP Right Cessation
- 1994-12-14 GB GB9425204A patent/GB2285065B/en not_active Expired - Fee Related
- 1994-12-14 DE DE69432783T patent/DE69432783T2/de not_active Expired - Lifetime
- 1994-12-14 EP EP94810726A patent/EP0659877B1/de not_active Expired - Lifetime
- 1994-12-20 IL IL112069A patent/IL112069A/en not_active IP Right Cessation
- 1994-12-20 NZ NZ270206A patent/NZ270206A/en not_active IP Right Cessation
- 1994-12-20 AU AU81608/94A patent/AU684116B2/en not_active Ceased
- 1994-12-21 US US08/361,257 patent/US6174854B1/en not_active Expired - Fee Related
- 1994-12-21 KR KR1019940035547A patent/KR100390226B1/ko not_active Expired - Fee Related
- 1994-12-22 ZA ZA9410243A patent/ZA9410243B/xx unknown
- 1994-12-22 BR BR9405213A patent/BR9405213A/pt not_active IP Right Cessation
- 1994-12-22 JP JP31895494A patent/JP3871720B2/ja not_active Expired - Fee Related
2000
- 2000-11-20 US US09/716,553 patent/US6398982B1/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
GB2285065A (en)	1995-06-28
IL112069A0 (en)	1995-03-15
KR950018411A (ko)	1995-07-22
DE69432783T2 (de)	2004-05-19
NZ270206A (en)	1995-08-28
US6174854B1 (en)	2001-01-16
EP0659877A2 (de)	1995-06-28
BR9405213A (pt)	1995-08-01
KR100390226B1 (ko)	2003-09-19
JPH07216740A (ja)	1995-08-15
EP0659877B1 (de)	2003-06-04
GB9326358D0 (en)	1994-02-23
GB2285065B (en)	1998-07-29
GB9425204D0 (en)	1995-02-15
US6398982B1 (en)	2002-06-04
JP3871720B2 (ja)	2007-01-24
ATE242307T1 (de)	2003-06-15
DE69432783D1 (de)	2003-07-10
ZA9410243B (en)	1995-06-23
ES2199951T3 (es)	2004-03-01
EP0659877A3 (de)	1996-03-13
AU684116B2 (en)	1997-12-04
AU8160894A (en)	1995-06-29

Legal Events

Date	Code	Title
1998-10-30	FF	Patent granted
1999-01-26	KB	Patent renewed
2005-09-25	MM9K	Patent not in force due to non-payment of renewal fees

Publication	Publication Date	Title
US6174854B1 (en)	2001-01-16	Composition for the treatment of textiles
EP0682145B1 (de)	2004-08-25	Textilbehandlungen
US5810889A (en)	1998-09-22	Aqueous textile treatment compositions containing an ultra-violet absorbing agent
US5688758A (en)	1997-11-18	Textile treatment
EP0850934B1 (de)	2004-03-10	Triazinylaminostilbene-Ultraviolett-absorbierenden Agenzien
GB2289290A (en)	1995-11-15	Textile Treatment
US6080208A (en)	2000-06-27	Stilbene compounds and their use
AU2002254958B2 (en)	2006-01-12	Fabric rinse composition containing a benztriazole UV absorber
AU2002254958A1 (en)	2003-03-27	Fabric rinse composition containing a benztriazole UV absorber
US20040103482A1 (en)	2004-06-03	Fabric rinse composition containing a cationic uv absorber
GB2290803A (en)	1996-01-10	Textile treatment
US20040078901A1 (en)	2004-04-29	Fabric rinse composition comprising a triazine uv absorber
MXPA97010436A (en)	1998-11-16	Compound
AU2002315254A1 (en)	2002-10-15	Fabric rinse composition comprising a triazine UV absorber
AU2002240950A1 (en)	2002-11-11	Fabric rinse composition containing a cationic UV absorber