JP2002503727A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2002503727A5 JP2002503727A5 JP2000532406A JP2000532406A JP2002503727A5 JP 2002503727 A5 JP2002503727 A5 JP 2002503727A5 JP 2000532406 A JP2000532406 A JP 2000532406A JP 2000532406 A JP2000532406 A JP 2000532406A JP 2002503727 A5 JP2002503727 A5 JP 2002503727A5
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- alkyl
- polyglycol
- hydroxyalkyl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
- 150000001875 compounds Chemical class 0.000 description 15
- 238000000034 method Methods 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 3
- 239000010695 polyglycol Substances 0.000 description 3
- -1 Phenylamino Chemical group 0.000 description 2
- 235000001014 amino acid Nutrition 0.000 description 2
- 125000000539 amino acid group Chemical group 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 2
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- NSMMFSKPGXCMOE-UHFFFAOYSA-N 2-[2-(2-sulfophenyl)ethenyl]benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1C=CC1=CC=CC=C1S(O)(=O)=O NSMMFSKPGXCMOE-UHFFFAOYSA-N 0.000 description 1
- REJHVSOVQBJEBF-OWOJBTEDSA-N 5-azaniumyl-2-[(e)-2-(4-azaniumyl-2-sulfonatophenyl)ethenyl]benzenesulfonate Chemical compound OS(=O)(=O)C1=CC(N)=CC=C1\C=C\C1=CC=C(N)C=C1S(O)(=O)=O REJHVSOVQBJEBF-OWOJBTEDSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- REJHVSOVQBJEBF-UHFFFAOYSA-N DSD-acid Natural products OS(=O)(=O)C1=CC(N)=CC=C1C=CC1=CC=C(N)C=C1S(O)(=O)=O REJHVSOVQBJEBF-UHFFFAOYSA-N 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 108010077895 Sarcosine Proteins 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 150000002431 hydrogen Chemical group 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229940043230 sarcosine Drugs 0.000 description 1
- 230000037072 sun protection Effects 0.000 description 1
- 229960003080 taurine Drugs 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP98810140 | 1998-02-20 | ||
| EP98810140.8 | 1998-02-20 | ||
| PCT/EP1999/000950 WO1999042454A1 (en) | 1998-02-20 | 1999-02-13 | A process for the preparation of stilbene compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002503727A JP2002503727A (ja) | 2002-02-05 |
| JP2002503727A5 true JP2002503727A5 (enExample) | 2006-04-13 |
Family
ID=8235955
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000532406A Withdrawn JP2002503727A (ja) | 1998-02-20 | 1999-02-13 | スチルベン化合物の製造方法 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US6365737B1 (enExample) |
| EP (1) | EP1054873B1 (enExample) |
| JP (1) | JP2002503727A (enExample) |
| KR (1) | KR100529488B1 (enExample) |
| CN (1) | CN1137107C (enExample) |
| AU (1) | AU759897B2 (enExample) |
| BR (1) | BR9908116A (enExample) |
| CA (1) | CA2319641A1 (enExample) |
| DE (1) | DE69920409T2 (enExample) |
| ES (1) | ES2228013T3 (enExample) |
| ID (1) | ID26102A (enExample) |
| IL (1) | IL137534A (enExample) |
| PL (1) | PL193440B1 (enExample) |
| RU (1) | RU2241703C2 (enExample) |
| WO (1) | WO1999042454A1 (enExample) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6165973A (en) * | 1999-02-05 | 2000-12-26 | Ciba Specialty Chemicals Corporation | Fluorescent whitening agent, its preparation and use |
| AU2917300A (en) | 1999-03-15 | 2000-10-04 | Ciba Specialty Chemicals Holding Inc. | Process for removing stain in a photographic material |
| WO2001023660A1 (en) * | 1999-09-30 | 2001-04-05 | The Procter & Gamble Company | Cotton fabric with durable properties |
| CN1326843C (zh) * | 2000-12-22 | 2007-07-18 | 富士胶片株式会社 | 二氨基-1,2-二苯乙烯衍生物 |
| BR0206398A (pt) * | 2001-01-12 | 2004-02-10 | Ciba Sc Holding Ag | Processo para a preparação de compostos do ácido triazinilaminoestilbeno-dissulfÈnico |
| GB0127903D0 (en) * | 2001-11-21 | 2002-01-16 | Clariant Int Ltd | Improvements relating to organic compounds |
| EP1511901B1 (en) * | 2002-06-11 | 2007-07-04 | Ciba SC Holding AG | Whitening pigments |
| WO2004046293A2 (en) * | 2002-11-19 | 2004-06-03 | Ciba Specialty Chemicals Holding Inc. | Amphoteric fluorescent whitening agents |
| WO2004069790A2 (en) * | 2003-02-10 | 2004-08-19 | Ciba Specialty Chemicals Holding Inc. | Crystalline modifications of triazinylaminostilbenes |
| EP1612209A1 (en) | 2004-06-28 | 2006-01-04 | Clariant International Ltd. | Improvements relating to optical brightening agents |
| CN101039924A (zh) * | 2004-10-20 | 2007-09-19 | 西巴特殊化学品控股有限公司 | 作为纸荧光增白剂的两性4,4′-二(三嗪基氨基)均二苯代乙烯-2,2′-二磺酸衍生物 |
| CN101048551B (zh) * | 2004-10-27 | 2012-02-15 | 西巴特殊化学品控股有限公司 | 荧光增白剂组合物 |
| RU2285719C1 (ru) * | 2005-04-18 | 2006-10-20 | Открытое акционерное общество "Химпром" | Состав для отбеливания текстильных материалов |
| KR100689260B1 (ko) * | 2005-05-24 | 2007-03-02 | 삼원산업주식회사 | 항산화성 스틸벤계 형광증백제 및 이의 합성방법 |
| EP1752453A1 (en) * | 2005-08-04 | 2007-02-14 | Clariant International Ltd. | Storage stable solutions of optical brighteners |
| WO2007048720A1 (en) * | 2005-10-24 | 2007-05-03 | Ciba Specialty Chemicals Holding Inc. | A composition for whitening paper |
| PL209690B1 (pl) * | 2005-11-24 | 2011-10-31 | Termo Organika Społka Z Ograniczoną Odpowiedzialnością | Sposób preparacji tworzyw, zabezpieczający przed działaniem promieniowania ultrafioletowego i ozonu |
| WO2008001368A2 (en) * | 2006-06-27 | 2008-01-03 | Hadasit Medical Research Services And Development Ltd. | Use of stilbene derivatives for treatment and prevention of aquatic mold infections |
| KR100907903B1 (ko) | 2007-07-30 | 2009-07-15 | 에스케이에너지 주식회사 | 아미노 트리아진이 치환된 스틸벤디설폰산나트륨염의제조방법 |
| PT2135997E (pt) * | 2008-06-11 | 2011-03-10 | Blankophor Gmbh & Co Kg | Composição e processo para branquear papel |
| EP2412870B1 (en) * | 2010-07-30 | 2013-04-17 | Blankophor GmbH & Co. KG | Composition and process for whitening paper |
| PT2518058E (pt) * | 2011-04-27 | 2014-11-25 | Clariant Int Ltd | Novos derivados de bis-(triazinilamino)-estilbeno |
| CA2839961C (en) * | 2011-06-21 | 2019-08-13 | Piramal Imaging Sa | Formulations of fluorinated stilbene suitable for pet imaging |
| KR101421622B1 (ko) | 2012-06-29 | 2014-07-23 | 삼원산업주식회사 | 항산화성 스틸벤계 형광증백의 합성방법 |
| CN103205134B (zh) * | 2013-03-14 | 2014-04-23 | 浙江传化华洋化工有限公司 | 一种dsd酸三嗪类荧光增白剂的合成方法 |
| PT2781648E (pt) * | 2013-03-21 | 2016-03-07 | Clariant Int Ltd | Agentes de branqueamento ótico para impressão a jato de tinta de alta qualidade |
| CN113717117A (zh) * | 2021-09-29 | 2021-11-30 | 浙江宏达化学制品有限公司 | 一种超声波辅助合成荧光增白剂的工艺 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4737240A (en) | 1985-05-02 | 1988-04-12 | Ciba-Geigy Corporation | Trisazo black dyes from 2-(4'-aminophenylazo)-7-amino-1-naphthol-3-sulfonic acid |
| GB8704328D0 (en) | 1987-02-24 | 1987-04-01 | Sandoz Products Ltd | Organic compounds |
| SU1646260A1 (ru) * | 1989-02-28 | 1995-01-27 | Л.В. Байгузова | Тетранатриевая соль 4,4'-бис-4-морфолино- 6-(n-сульфоанилино)- сим-триазинил-2-ил- аминостильбен-2,2'- дисульфокислоты в качестве оптически отбеливающего вещества |
| ES2104881T3 (es) | 1991-09-26 | 1997-10-16 | Ciba Geigy Ag | Procedimiento para teñir papel con colorantes diazoicos. |
| GB9418958D0 (en) * | 1994-09-21 | 1994-11-09 | Ciba Geigy Ag | Fluorescent whitening agents |
| DE19500791C1 (de) * | 1995-01-13 | 1996-08-01 | Bayer Ag | Verfahren zur Herstellung von substituierten 4,4'-Diaminostilben-2,2'-disulfonsäuresalzen |
| GB9503474D0 (en) * | 1995-02-22 | 1995-04-12 | Ciba Geigy Ag | Compounds and their use |
-
1999
- 1999-02-13 US US09/622,472 patent/US6365737B1/en not_active Expired - Fee Related
- 1999-02-13 ES ES99908890T patent/ES2228013T3/es not_active Expired - Lifetime
- 1999-02-13 CN CNB998030856A patent/CN1137107C/zh not_active Expired - Fee Related
- 1999-02-13 AU AU28337/99A patent/AU759897B2/en not_active Ceased
- 1999-02-13 KR KR10-2000-7009102A patent/KR100529488B1/ko not_active Expired - Fee Related
- 1999-02-13 EP EP99908890A patent/EP1054873B1/en not_active Expired - Lifetime
- 1999-02-13 DE DE69920409T patent/DE69920409T2/de not_active Expired - Fee Related
- 1999-02-13 RU RU2000124270/04A patent/RU2241703C2/ru not_active IP Right Cessation
- 1999-02-13 CA CA002319641A patent/CA2319641A1/en not_active Abandoned
- 1999-02-13 IL IL13753499A patent/IL137534A/xx active IP Right Grant
- 1999-02-13 BR BR9908116-4A patent/BR9908116A/pt not_active Application Discontinuation
- 1999-02-13 ID IDW20001777A patent/ID26102A/id unknown
- 1999-02-13 JP JP2000532406A patent/JP2002503727A/ja not_active Withdrawn
- 1999-02-13 WO PCT/EP1999/000950 patent/WO1999042454A1/en not_active Ceased
- 1999-02-13 PL PL99342469A patent/PL193440B1/pl unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2002503727A5 (enExample) | ||
| RU2000124270A (ru) | Способ получения соединений стильбена | |
| JP4243483B2 (ja) | 蛍光増白剤組成物、それらの製造およびそれらの使用 | |
| JP2002536501A5 (enExample) | ||
| AU2005279193B2 (en) | Shading process | |
| AU768659B2 (en) | Fluorescent whitening agent, its preparation and use | |
| TW201116663A (en) | Disulfo-type fluorescent whitening agent compositions | |
| ES2525151T3 (es) | Nuevos derivados de bis-(triacinilamino)-estilbeno | |
| BR9908116A (pt) | Processo para a preparação de compostos de estilbeno | |
| JP2007526383A (ja) | 濃厚蛍光増白剤溶液 | |
| TW201245542A (en) | Fluorescent whitening agent compositions | |
| ZA200503105B (en) | Amphoteric fluorescent whitening agents | |
| JP2011507988A (ja) | 蛍光増白剤の貯蔵安定性溶液 | |
| JPH10226680A (ja) | 置換4、4′−ジアミノスチルベン−2、2′−ジスルホン酸の製造法 | |
| JPH08119946A (ja) | 蛍光増白剤 | |
| CA2425165A1 (en) | A process for the preparation of bis-benzazolyl compounds | |
| JPS596260A (ja) | 金属化されたジスアゾ化合物 | |
| JPH09165526A5 (enExample) | ||
| HUP0102666A2 (hu) | Eljárás 2,4-imidazolidindion-származék előállítására | |
| TW588015B (en) | Nonaborate compositions and their preparation | |
| CN1173888A (zh) | 活性偶氮染料的制备方法 | |
| KR100735711B1 (ko) | 형광 증백제 및 이의 합성방법 | |
| EP0873989A3 (en) | Process for the preparation of distyryl-biphenyl compounds | |
| ITMI20111449A1 (it) | Soluzioni acquose di agenti sbiancanti fluorescenti | |
| KR100847235B1 (ko) | 디스아조 염료의 구리 착물을 사용하는 천연 재료 또는 합성 재료의 염색방법 |