RU99122588A - FLUORESCENT BLEACHING PRODUCTS - Google Patents
FLUORESCENT BLEACHING PRODUCTSInfo
- Publication number
- RU99122588A RU99122588A RU99122588/04A RU99122588A RU99122588A RU 99122588 A RU99122588 A RU 99122588A RU 99122588/04 A RU99122588/04 A RU 99122588/04A RU 99122588 A RU99122588 A RU 99122588A RU 99122588 A RU99122588 A RU 99122588A
- Authority
- RU
- Russia
- Prior art keywords
- formula
- paper
- indicated above
- fluorescent whitening
- represents hydrogen
- Prior art date
Links
- 238000004061 bleaching Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 11
- 229910052739 hydrogen Inorganic materials 0.000 claims 11
- 239000001257 hydrogen Substances 0.000 claims 10
- 239000004753 textile Substances 0.000 claims 8
- 239000000463 material Substances 0.000 claims 7
- 230000002087 whitening Effects 0.000 claims 7
- 125000000217 alkyl group Chemical group 0.000 claims 6
- 239000003599 detergent Substances 0.000 claims 6
- 150000002431 hydrogen Chemical group 0.000 claims 6
- 239000003795 chemical substances by application Substances 0.000 claims 5
- 239000006081 fluorescent whitening agent Substances 0.000 claims 4
- DHMQDGOQFOQNFH-UHFFFAOYSA-N glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 4
- 150000002978 peroxides Chemical class 0.000 claims 4
- 125000000539 amino acid group Chemical group 0.000 claims 3
- 239000002657 fibrous material Substances 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- 239000002736 nonionic surfactant Substances 0.000 claims 3
- 239000004471 Glycine Substances 0.000 claims 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims 2
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims 2
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 claims 2
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 claims 2
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims 2
- 239000012190 activator Substances 0.000 claims 2
- 239000002671 adjuvant Substances 0.000 claims 2
- 230000000240 adjuvant Effects 0.000 claims 2
- 229910052783 alkali metal Inorganic materials 0.000 claims 2
- 150000001340 alkali metals Chemical group 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- 125000003277 amino group Chemical group 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 2
- 239000003945 anionic surfactant Substances 0.000 claims 2
- 239000011230 binding agent Substances 0.000 claims 2
- 239000007844 bleaching agent Substances 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 150000001768 cations Chemical class 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 239000004744 fabric Substances 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- -1 hydroxy, thio, methylthio, amino, carboxy, sulfo, phenyl Chemical group 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 238000007493 shaping process Methods 0.000 claims 2
- 239000000758 substrate Substances 0.000 claims 2
- 239000012463 white pigment Substances 0.000 claims 2
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 229960005261 Aspartic Acid Drugs 0.000 claims 1
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N DL-alanine Chemical compound CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 claims 1
- FFEARJCKVFRZRR-UHFFFAOYSA-N DL-methionine Chemical compound CSCCC(N)C(O)=O FFEARJCKVFRZRR-UHFFFAOYSA-N 0.000 claims 1
- 102000004190 Enzymes Human genes 0.000 claims 1
- 108090000790 Enzymes Proteins 0.000 claims 1
- 229960002989 Glutamic Acid Drugs 0.000 claims 1
- 229960000310 ISOLEUCINE Drugs 0.000 claims 1
- CKLJMWTZIZZHCS-UWTATZPHSA-N L-Aspartic acid Natural products OC(=O)[C@H](N)CC(O)=O CKLJMWTZIZZHCS-UWTATZPHSA-N 0.000 claims 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims 1
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 claims 1
- 239000004395 L-leucine Substances 0.000 claims 1
- 235000019454 L-leucine Nutrition 0.000 claims 1
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 claims 1
- 229960005190 Phenylalanine Drugs 0.000 claims 1
- 229960002429 Proline Drugs 0.000 claims 1
- 229920001131 Pulp (paper) Polymers 0.000 claims 1
- 239000004473 Threonine Substances 0.000 claims 1
- 239000000853 adhesive Substances 0.000 claims 1
- 230000000844 anti-bacterial Effects 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- 239000003899 bactericide agent Substances 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 238000005260 corrosion Methods 0.000 claims 1
- 239000006185 dispersion Substances 0.000 claims 1
- 239000000975 dye Substances 0.000 claims 1
- 239000003995 emulsifying agent Substances 0.000 claims 1
- 239000002979 fabric softener Substances 0.000 claims 1
- 239000000835 fiber Substances 0.000 claims 1
- 239000007850 fluorescent dye Substances 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 229960003136 leucine Drugs 0.000 claims 1
- 239000003605 opacifier Substances 0.000 claims 1
- 230000003287 optical Effects 0.000 claims 1
- 239000002304 perfume Substances 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 230000037072 sun protection Effects 0.000 claims 1
- 229960002898 threonine Drugs 0.000 claims 1
- 210000001519 tissues Anatomy 0.000 claims 1
- 229960004295 valine Drugs 0.000 claims 1
- 238000005406 washing Methods 0.000 claims 1
Claims (15)
где Х представляет О или NH; М представляет водород, атом щелочного металла, аммоний или катион, образованный из амина; каждый R1 независимо представляет аминокислотный остаток, из которого был удален атом водорода на аминогруппе; n равно 1 или 2; а каждый R2 независимо представляет водород, C1-С3алкил, галоген, циано, COOR, где R представляет водород или C1-С3алкил, CONH-R, где R представляет значение, указанное выше, SO2NH-R, где R имеет значение, указанное выше, NH-COR, где R имеет значение, указанное выше, SО3М, где М имеет значение, указанное выше; или, если n равно 1, то R2 может также быть СО-R3, где R3 представляет C1-С3алкил или фенил;
при условии, что исключены такие соединения, в которых:
a) Х представляет NH, n равно 1, a R2 представляет SО3М, где М имеет значение, указанное выше; или
b) Х представляет NH, n равно 2, и один из R2 представляет SО3М, где М имеет значение, указанное выше, а другой R2 представляет водород, метил или галоген, или
c) Х представляет NH, n равно 1, R1 представляет глицин, a R2 представляет Н или СO2Н; или
d) Х представляет NH, n равно 2, каждый из R2 представляет SО3М, где М имеет значение, указанное выше, а группы SО3М находятся в 2,5-положениях фенильного кольца, и R1 представляет D,L-аланин, L-валин, L-лейцин, L-изолейцин, L-треонин, L-аспарагиновую кислоту, L-глутаминовую кислоту, L-фенилаланин, L-пролин, D,L-метионин или глицин.1. The compound having the formula:
where X represents O or NH; M represents hydrogen, an alkali metal atom, ammonium or a cation formed from an amine; each R 1 independently represents an amino acid residue from which a hydrogen atom on an amino group has been removed; n is 1 or 2; and each R 2 independently represents hydrogen, C 1 -C 3 alkyl, halogen, cyano, COOR, where R represents hydrogen or C 1 -C 3 alkyl, CONH-R, where R represents the value indicated above, SO 2 NH-R where R has the meaning indicated above, NH-COR, where R has the meaning indicated above, SO 3 M, where M has the meaning indicated above; or, if n is 1, then R 2 may also be CO-R 3 , where R 3 is C 1 -C 3 alkyl or phenyl;
provided that such compounds are excluded in which:
a) X is NH, n is 1, and R 2 is SO 3 M, where M is as defined above; or
b) X is NH, n is 2, and one of R 2 is SO 3 M, where M is as defined above and the other R 2 is hydrogen, methyl or halogen, or
c) X is NH, n is 1, R 1 is glycine, and R 2 is H or CO 2 H; or
d) X is NH, n is 2, each of R 2 is SO 3 M, where M is as defined above, and SO 3 M groups are in the 2,5-positions of the phenyl ring, and R 1 is D, L- alanine, L-valine, L-leucine, L-isoleucine, L-threonine, L-aspartic acid, L-glutamic acid, L-phenylalanine, L-proline, D, L-methionine or glycine.
где X представляет О или NH; М представляет водород, атом щелочного металла, аммоний или катион, образованный из амина; каждый R1 независимо представляет аминокислотный остаток, из которого был удален атом водорода на аминогруппе; n равно 1 или 2; а каждый R'2 независимо представляет водород, C1-С3алкил, галоген, циано, COOR, где R представляет водород или C1-С3алкил, CONH-R, где R имеет значение, указанное выше, SO2NH-R, где R имеет значение, указанное выше, NH-COR, где R имеет значение, указанное выше, или SО3М, где М имеет значение, указанное выше;
при условии, что исключены соединения, в которых Х представляет NH, n равно 2, и один из R2 представляет SО3М, где М имеет значение, указанное выше, а другой R2 представляет водород, метил или галоген.3. A method of fluorescent whitening of a substrate, comprising contacting the substrate with a compound of formula (1A):
where X represents O or NH; M represents hydrogen, an alkali metal atom, ammonium or a cation formed from an amine; each R 1 independently represents an amino acid residue from which a hydrogen atom on an amino group has been removed; n is 1 or 2; and each R ′ 2 independently represents hydrogen, C 1 -C 3 alkyl, halogen, cyano, COOR, where R represents hydrogen or C 1 -C 3 alkyl, CONH-R, where R has the meaning indicated above, SO 2 NH- R, where R has the meaning indicated above, NH-COR, where R has the meaning indicated above, or SO 3 M, where M has the meaning indicated above;
with the proviso that compounds in which X is NH, n is 2, and one of R 2 is SO 3 M, where M is as defined above and the other R 2 is hydrogen, methyl or halogen, are excluded.
i) 5 - 90% анионогенного поверхностно-активного вещества и/или неионогенного поверхностно-активного вещества;
ii) 5 - 70% агента, придающего форму;
iii) 0 - 30% пероксида;
iv) 0 - 10% пероксидного активатора, и/или 0 - 1% катализатора отбеливания;
v) 0,005 - 2% по крайней мере, одного из соединений формулы 1А; и
vi) 0,005 - 10% одного или нескольких вспомогательных агентов, где количество каждого компонента взято исходя из общей массы моющего средства.11. The method of claim 10, wherein the detergent composition used comprises:
i) 5 to 90% of an anionic surfactant and / or a nonionic surfactant;
ii) 5 to 70% of a shaping agent;
iii) 0-30% peroxide;
iv) 0-10% peroxide activator and / or 0-1% whitening catalyst;
v) 0.005 - 2% of at least one of the compounds of formula 1A; and
vi) 0.005 - 10% of one or more auxiliary agents, where the amount of each component is taken based on the total weight of the detergent.
i) 5 - 90% анионогенного поверхностно-активного вещества и/или неионогенного поверхностно-активного вещества;
ii) 5 - 70% агента, придающего форму;
iii) 0 - 30% пероксида;
iv) 0 - 10% пероксидного активатора, и/или 0 - 1% катализатора отбеливания;
v) 0,005 - 2% по крайней мере, одного из соединений формулы 1А по п.7, и
vi) 0,005 - 10% одного или нескольких вспомогательных агентов, где количество каждого компонента взято исходя из общей массы моющего средства.13. A detergent composition comprising:
i) 5 to 90% of an anionic surfactant and / or a nonionic surfactant;
ii) 5 to 70% of a shaping agent;
iii) 0-30% peroxide;
iv) 0-10% peroxide activator and / or 0-1% whitening catalyst;
v) 0.005 - 2% of at least one of the compounds of formula 1A according to claim 7, and
vi) 0.005 - 10% of one or more auxiliary agents, where the amount of each component is taken based on the total weight of the detergent.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9706110.5 | 1997-03-25 | ||
GBGB9706110.5A GB9706110D0 (en) | 1997-03-25 | 1997-03-25 | Compounds |
GB9709980.8 | 1997-05-17 | ||
GBGB9709980.8A GB9709980D0 (en) | 1997-05-17 | 1997-05-17 | Compounds |
Publications (2)
Publication Number | Publication Date |
---|---|
RU99122588A true RU99122588A (en) | 2001-08-20 |
RU2198168C2 RU2198168C2 (en) | 2003-02-10 |
Family
ID=26311253
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU99122588/04A RU2198168C2 (en) | 1997-03-25 | 1998-03-14 | Fluorescent bleaching agents |
Country Status (15)
Country | Link |
---|---|
US (3) | US6210449B1 (en) |
EP (2) | EP0971905B1 (en) |
JP (1) | JP2001518919A (en) |
KR (1) | KR100519872B1 (en) |
CN (1) | CN1168723C (en) |
AT (2) | ATE244227T1 (en) |
AU (1) | AU6831498A (en) |
BR (1) | BR9808058B1 (en) |
CA (1) | CA2284723A1 (en) |
DE (2) | DE69816135T2 (en) |
ES (1) | ES2226117T3 (en) |
ID (1) | ID22819A (en) |
NO (1) | NO314083B1 (en) |
RU (1) | RU2198168C2 (en) |
WO (1) | WO1998042685A1 (en) |
Families Citing this family (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9726365D0 (en) * | 1997-12-13 | 1998-02-11 | Ciba Sc Holding Ag | Compounds |
EP1166179A1 (en) * | 1999-03-15 | 2002-01-02 | Ciba SC Holding AG | Process for removing stain in a photographic material |
WO2000077290A2 (en) * | 1999-06-11 | 2000-12-21 | Ciba Specialty Chemicals Holding Inc. | Use of uv absorbers for suppressing the fluorescence of textile fibre materials treated with fluorescent whitening agents |
KR20020087043A (en) * | 1999-09-10 | 2002-11-21 | 시바 스페셜티 케미칼스 홀딩 인크. | Triazinylaminostilbene derivative as fluorescent whitening agents |
ATE306537T1 (en) * | 2000-06-19 | 2005-10-15 | Ciba Sc Holding Ag | FLUORESCENT BRIGHTENING PIGMENT COMPOSITIONS |
CN1486303A (en) * | 2001-01-12 | 2004-03-31 | �������⻯ѧƷ�ع�����˾ | Process for the preparation of triazinylaminostilbene-disulphonic acid compounds |
GB0125177D0 (en) * | 2001-10-19 | 2001-12-12 | Clariant Int Ltd | Improvements in or relating to organic compounds |
BR0311712A (en) * | 2002-06-11 | 2005-03-15 | Ciba Sc Holding Ag | Bleaching pigments |
US7270771B2 (en) * | 2002-07-05 | 2007-09-18 | Ciba Specialty Chemicals Corporation | Triazinylaminostilbene disulphonic acid mixtures |
FI122297B (en) * | 2003-10-27 | 2011-11-15 | M Real Oyj | Cardboard and the method used to make it |
EP1571149A1 (en) * | 2004-03-05 | 2005-09-07 | Clariant International Ltd. | Optical brightener solutions |
EP1612209A1 (en) | 2004-06-28 | 2006-01-04 | Clariant International Ltd. | Improvements relating to optical brightening agents |
DE102004038578A1 (en) * | 2004-08-06 | 2006-03-16 | Lanxess Deutschland Gmbh | Alkanolammonium-containing Triazinylflavonataufheller |
DE602005022622D1 (en) * | 2004-12-09 | 2010-09-09 | Clariant Finance Bvi Ltd | AQUEOUS DISPERSION OPTICAL LIGHTER |
EP1712677A1 (en) | 2005-04-08 | 2006-10-18 | Clariant International Ltd. | Aqueous solutions of optical brighteners |
KR100735711B1 (en) | 2006-01-09 | 2007-07-06 | 삼원산업주식회사 | Fluorescent whitening agent and process of producing thereof |
SE530020C2 (en) * | 2006-06-15 | 2008-02-12 | Holmen Ab | Method for stabilizing the whiteness of surface treatment adhesive / smear for paper containing flurorescent whitening agent (FWA) and of this / these shaped surface treatment layers |
EP1881108A1 (en) * | 2006-07-18 | 2008-01-23 | CIBA SPECIALTY CHEMICALS HOLDING INC. Patent Departement | Fluorescent Whitening Compositions |
KR20090058516A (en) * | 2006-08-08 | 2009-06-09 | 클라리언트 파이넌스 (비브이아이)리미티드 | Aqueous solutions of optical brighteners |
US7445567B2 (en) * | 2006-12-13 | 2008-11-04 | Bridgestone Sports Co., Ltd. | Multi-piece solid golf ball |
CA2719543C (en) | 2008-03-26 | 2016-05-31 | Clariant Finance (Bvi) Limited | Improved optical brightening compositions |
AU2014259497B2 (en) * | 2008-03-26 | 2016-05-12 | Archroma Ip Gmbh | Improved optical brightening compositions |
PT2135997E (en) * | 2008-06-11 | 2011-03-10 | Blankophor Gmbh & Co Kg | Composition and process for whitening paper |
EP2356183B2 (en) * | 2008-12-08 | 2021-01-27 | Hewlett-Packard Development Company, L.P. | Surface coating composition for inkjet media |
PL2302132T3 (en) * | 2009-09-17 | 2013-01-31 | Blankophor Gmbh & Co Kg | Disulfo-type fluorescent whitening agents |
CN102906239B (en) | 2010-05-18 | 2015-09-09 | 美利肯公司 | White dyes and containing its composition |
ES2433917T3 (en) | 2010-09-17 | 2013-12-13 | Blankophor Gmbh & Co. Kg | Composition of fluorescent bleaching agents |
EP2518058B1 (en) * | 2011-04-27 | 2014-10-29 | Clariant International Ltd. | Novel bis-(triazinylamino)-stilbene derivatives |
CN102311657B (en) * | 2011-06-25 | 2013-12-11 | 山东大学 | Low-water-solubility fluorescent whitening agent with bactericidal action as well as synthesis method and application thereof |
CN102898855B (en) * | 2012-09-29 | 2013-12-11 | 山东大学 | Synthesis and application of cetyl or octadecyl dimethyl tertiary amine quaternary ammonium salt high performance fluorescent whitening agent having amino acid structure |
EP2781648B1 (en) * | 2013-03-21 | 2016-01-06 | Clariant International Ltd. | Optical brightening agents for high quality ink-jet printing |
FR3013591B1 (en) * | 2013-11-28 | 2019-06-14 | L'oreal | COSMETIC METHOD FOR LIGHTENING THE SKIN WITH ANIONIC OPTICAL AZURANT |
US9487503B2 (en) * | 2014-04-17 | 2016-11-08 | 3V Sigma S.P.A. | Stilbene optical brighteners |
EP3346052A4 (en) | 2015-08-31 | 2019-05-01 | Shima Seiki Mfg., Ltd | Method for manufacturing processed fiber, processed fiber, method for suppressing damage to animal fiber, and method for processing animal fiber |
CN105482488A (en) * | 2015-11-25 | 2016-04-13 | 山西青山化工有限公司 | Liquid fluorescent whitener and preparation method thereof |
WO2017128201A1 (en) * | 2016-01-28 | 2017-08-03 | 德丰铭国际股份有限公司 | Fluorescent whitening agent composition |
WO2017162918A1 (en) * | 2016-03-22 | 2017-09-28 | Åbo Akademi University | Polysaccharide derivatives as optical brightening agents |
CN106632116B (en) * | 2016-12-20 | 2019-08-13 | 贺州学院 | A kind of water solubility heavy calcium carbonate powder fluorescent whitening agent and its preparation method and application |
CN107311952A (en) * | 2017-07-06 | 2017-11-03 | 广西碳酸钙产业化工程院有限公司 | A kind of preparation method and applications of calcium carbonate powder brightening agent and surfactant |
ES2904846T3 (en) | 2017-12-22 | 2022-04-06 | Archroma Ip Gmbh | Optical brightener to whiten paper |
WO2021061713A1 (en) * | 2019-09-27 | 2021-04-01 | B&B Blending, Llc | Use of a fluorescent optical brightener or phosphorescent indicator within ceramic coatings for visual detection and identification |
CN110922531B (en) * | 2019-12-06 | 2022-06-24 | 陕西科技大学 | Starch grafted fluorescent copolymer emulsion and preparation method and application thereof |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DD20974A (en) * | ||||
DE20974C (en) * | H. REUSCH, Ober-Bergrath a. D. in Dillingen a. Saar | Process for plating iron and steel | ||
DE20794C (en) | L. RÖ.SSLER in Altenmarkt a. Alz, Ober-Bayern | Malt peeling machine | ||
DE1011889B (en) * | 1956-06-14 | 1957-07-11 | Cassella Farbwerke Mainkur Ag | Process for the manufacture of optical bleaching agents |
GB1008457A (en) | 1963-04-12 | 1965-10-27 | Gen Aniline & Film Corp | Improvements in or relating to stilbene-cyanuric compounds |
GB1021527A (en) | 1963-04-12 | 1966-03-02 | Gen Aniline & Film Corp | Improvements in or relating to stilbene-cyanuric compounds |
DE1469218B1 (en) * | 1964-06-30 | 1971-09-08 | Hoechst Ag | 4,4'-bis-triazinylamino-stilbene compounds and their use as reactive optical brightening agents |
NL6714386A (en) * | 1967-10-23 | 1969-04-25 | ||
GB1238833A (en) | 1968-01-18 | 1971-07-14 | ||
DE2700293A1 (en) | 1977-01-05 | 1978-07-06 | Bayer Ag | DYE LASER |
JPS62106965A (en) * | 1985-11-05 | 1987-05-18 | Shin Nisso Kako Co Ltd | Fluorescent brightener |
JPS63282382A (en) * | 1987-05-14 | 1988-11-18 | 日本化薬株式会社 | Dyeing method |
GB9412590D0 (en) * | 1994-06-23 | 1994-08-10 | Sandoz Ltd | Organic compounds |
GB9503474D0 (en) * | 1995-02-22 | 1995-04-12 | Ciba Geigy Ag | Compounds and their use |
GB2313850A (en) | 1996-06-04 | 1997-12-10 | Ciba Geigy Ag | Triazine based UVA compounds as quenchers in paper making processes |
GB9611614D0 (en) * | 1996-06-04 | 1996-08-07 | Ciba Geigy Ag | Process for inhibiting the effect of flourescent whitening agents |
-
1998
- 1998-03-14 AU AU68314/98A patent/AU6831498A/en not_active Abandoned
- 1998-03-14 AT AT01111295T patent/ATE244227T1/en not_active IP Right Cessation
- 1998-03-14 ID IDW991234A patent/ID22819A/en unknown
- 1998-03-14 CN CNB988037289A patent/CN1168723C/en not_active Expired - Fee Related
- 1998-03-14 JP JP54482598A patent/JP2001518919A/en active Pending
- 1998-03-14 EP EP98913720A patent/EP0971905B1/en not_active Expired - Lifetime
- 1998-03-14 WO PCT/EP1998/001495 patent/WO1998042685A1/en active IP Right Grant
- 1998-03-14 DE DE69816135T patent/DE69816135T2/en not_active Expired - Lifetime
- 1998-03-14 BR BRPI9808058-0A patent/BR9808058B1/en not_active IP Right Cessation
- 1998-03-14 DE DE69825574T patent/DE69825574T2/en not_active Expired - Lifetime
- 1998-03-14 CA CA002284723A patent/CA2284723A1/en not_active Abandoned
- 1998-03-14 AT AT98913720T patent/ATE273290T1/en not_active IP Right Cessation
- 1998-03-14 US US09/381,468 patent/US6210449B1/en not_active Expired - Fee Related
- 1998-03-14 EP EP01111295A patent/EP1123929B1/en not_active Expired - Lifetime
- 1998-03-14 KR KR10-1999-7008739A patent/KR100519872B1/en not_active IP Right Cessation
- 1998-03-14 ES ES98913720T patent/ES2226117T3/en not_active Expired - Lifetime
- 1998-03-14 RU RU99122588/04A patent/RU2198168C2/en not_active IP Right Cessation
-
1999
- 1999-09-24 NO NO19994662A patent/NO314083B1/en not_active IP Right Cessation
-
2001
- 2001-01-22 US US09/766,984 patent/US6464735B2/en not_active Expired - Fee Related
- 2001-01-22 US US09/767,112 patent/US6458169B2/en not_active Expired - Fee Related
Similar Documents
Publication | Publication Date | Title |
---|---|---|
RU99122588A (en) | FLUORESCENT BLEACHING PRODUCTS | |
RU2198168C2 (en) | Fluorescent bleaching agents | |
ES2228013T3 (en) | A PROCEDURE FOR THE PREPARATION OF STILBENE COMPOUNDS. | |
KR20020087043A (en) | Triazinylaminostilbene derivative as fluorescent whitening agents | |
RU2000124270A (en) | METHOD OF OBTAINING STYLBENE COMPOUNDS | |
NO965487L (en) | Optical whitening agents | |
RU2005102918A (en) | MIXTURES OF DISULPHIC ACIDS OF TRIAZINYLAMINOSTINESIS | |
KR970074774A (en) | Stilbene Compounds and Uses thereof | |
ATE86474T1 (en) | METHOD OF DYING KERATINE FIBERS WITH MONOHYDROXYINDOL AND HYDROXYINDOL 5,6DISUBSTITUTED AND COMPOSITION. | |
CN1492866A (en) | Bis-triazinylaminobenzoxazole derivatives | |
JPH0451599B2 (en) | ||
TH46773A (en) | Reactive dye compounds | |
MXPA98010407A (en) | Asymmetric estilb compounds | |
RU98101720A (en) | CONTAINING PEROXIDE BLEACH COMPOSITIONS WITH POLYAMINE STABILIZERS FOR PRELIMINARY SPOT PROCESSING, ENSURING IMPROVED CONSERVATION OF FABRIC AND DYE | |
MXPA99008749A (en) | Fluorescent whitening agents |