JPH0450944B2 - - Google Patents

Info

Publication number: JPH0450944B2
Authority: JP; Japan
Prior art keywords: group; formula; acid; parts; methyl
Prior art date: 1984-01-25
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.): Expired

Application number

JP1022884A

Other languages

English (en)

Japanese (ja)

Other versions

JPS60156759A (ja

Inventor

Tadashi Matsuo

Junko Inoe

Yutaka Hirasawa

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Nippon Kayaku Co Ltd

Original Assignee

Nippon Kayaku Co Ltd

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.)

1984-01-25

Filing date

1984-01-25

Publication date

1992-08-17

1984-01-25 Application filed by Nippon Kayaku Co Ltd filed Critical Nippon Kayaku Co Ltd

1984-01-25 Priority to JP1022884A priority Critical patent/JPS60156759A/ja

1985-08-16 Publication of JPS60156759A publication Critical patent/JPS60156759A/ja

1992-08-17 Publication of JPH0450944B2 publication Critical patent/JPH0450944B2/ja

Status Granted legal-status Critical Current

Links

-1 N-methyl-N-acetylamino group Chemical group 0.000 claims description 63
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 10
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 10
239000002253 acid Substances 0.000 claims description 9
125000003277 amino group Chemical group 0.000 claims description 9
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 4
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims description 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
125000000542 sulfonic acid group Chemical group 0.000 claims description 3
125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 2
125000001624 naphthyl group Chemical group 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
150000001875 compounds Chemical class 0.000 description 28
KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 description 17
HBZVNWNSRNTWPS-UHFFFAOYSA-N 6-amino-4-hydroxynaphthalene-2-sulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C(O)C2=CC(N)=CC=C21 HBZVNWNSRNTWPS-UHFFFAOYSA-N 0.000 description 13
239000004372 Polyvinyl alcohol Substances 0.000 description 12
229920002451 polyvinyl alcohol Polymers 0.000 description 12
235000002639 sodium chloride Nutrition 0.000 description 12
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
239000000243 solution Substances 0.000 description 10
238000006243 chemical reaction Methods 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
238000010521 absorption reaction Methods 0.000 description 6
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
239000003086 colorant Substances 0.000 description 4
238000004043 dyeing Methods 0.000 description 4
238000000034 method Methods 0.000 description 4
239000002244 precipitate Substances 0.000 description 4
239000011780 sodium chloride Substances 0.000 description 4
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 4
NAZDVUBIEPVUKE-UHFFFAOYSA-N 2,5-dimethoxyaniline Chemical compound COC1=CC=C(OC)C(N)=C1 NAZDVUBIEPVUKE-UHFFFAOYSA-N 0.000 description 3
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
238000007796 conventional method Methods 0.000 description 3
229910052740 iodine Inorganic materials 0.000 description 3
239000011630 iodine Substances 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
230000010287 polarization Effects 0.000 description 3
RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 2
VOWZNBNDMFLQGM-UHFFFAOYSA-N 2,5-dimethylaniline Chemical group CC1=CC=C(C)C(N)=C1 VOWZNBNDMFLQGM-UHFFFAOYSA-N 0.000 description 2
JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 2
QEZZCWMQXHXAFG-UHFFFAOYSA-N 8-aminonaphthalene-2-sulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C2C(N)=CC=CC2=C1 QEZZCWMQXHXAFG-UHFFFAOYSA-N 0.000 description 2
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
229920000297 Rayon Polymers 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
235000011114 ammonium hydroxide Nutrition 0.000 description 2
229910000365 copper sulfate Inorganic materials 0.000 description 2
ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 2
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
239000000463 material Substances 0.000 description 2
239000000203 mixture Substances 0.000 description 2
238000005185 salting out Methods 0.000 description 2
235000011121 sodium hydroxide Nutrition 0.000 description 2
235000010288 sodium nitrite Nutrition 0.000 description 2
229910052979 sodium sulfide Inorganic materials 0.000 description 2
GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 2
238000000859 sublimation Methods 0.000 description 2
230000008022 sublimation Effects 0.000 description 2
239000000758 substrate Substances 0.000 description 2
XPKFTIYOZUJAGA-UHFFFAOYSA-N 2,5-diethoxyaniline Chemical compound CCOC1=CC=C(OCC)C(N)=C1 XPKFTIYOZUJAGA-UHFFFAOYSA-N 0.000 description 1
TUOWYJFPLMIKCX-UHFFFAOYSA-N 2-ethoxynaphthalen-1-amine Chemical compound C1=CC=CC2=C(N)C(OCC)=CC=C21 TUOWYJFPLMIKCX-UHFFFAOYSA-N 0.000 description 1
FAOJNWOJCPKVTM-UHFFFAOYSA-N 2-methoxynaphthalen-1-amine Chemical compound C1=CC=CC2=C(N)C(OC)=CC=C21 FAOJNWOJCPKVTM-UHFFFAOYSA-N 0.000 description 1
ZCNCWYFISJTFHB-UHFFFAOYSA-N 4-hydroxy-7-(methylamino)naphthalene-2-sulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=CC(NC)=CC=C21 ZCNCWYFISJTFHB-UHFFFAOYSA-N 0.000 description 1
YGNDWDUEMICDLW-UHFFFAOYSA-N 7-anilino-4-hydroxynaphthalene-2-sulfonic acid Chemical compound C=1C=C2C(O)=CC(S(O)(=O)=O)=CC2=CC=1NC1=CC=CC=C1 YGNDWDUEMICDLW-UHFFFAOYSA-N 0.000 description 1
ZLHGMJOGMLVDFS-UHFFFAOYSA-N 7-benzamido-4-hydroxynaphthalene-2-sulfonic acid Chemical compound C=1C=C2C(O)=CC(S(O)(=O)=O)=CC2=CC=1NC(=O)C1=CC=CC=C1 ZLHGMJOGMLVDFS-UHFFFAOYSA-N 0.000 description 1
229920000298 Cellophane Polymers 0.000 description 1
229920003043 Cellulose fiber Polymers 0.000 description 1
OVBJJZOQPCKUOR-UHFFFAOYSA-L EDTA disodium salt dihydrate Chemical compound O.O.[Na+].[Na+].[O-]C(=O)C[NH+](CC([O-])=O)CC[NH+](CC([O-])=O)CC([O-])=O OVBJJZOQPCKUOR-UHFFFAOYSA-L 0.000 description 1
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 1
239000004677 Nylon Substances 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000003973 alkyl amines Chemical class 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
238000004040 coloring Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
239000012954 diazonium Substances 0.000 description 1
150000001989 diazonium salts Chemical class 0.000 description 1
238000006193 diazotization reaction Methods 0.000 description 1
150000002169 ethanolamines Chemical class 0.000 description 1
125000004464 hydroxyphenyl group Chemical group 0.000 description 1
229910003002 lithium salt Inorganic materials 0.000 description 1
159000000002 lithium salts Chemical class 0.000 description 1
239000011259 mixed solution Substances 0.000 description 1
LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
SJWQCBCAGCEWCV-UHFFFAOYSA-N n-(3-amino-4-methoxyphenyl)acetamide Chemical compound COC1=CC=C(NC(C)=O)C=C1N SJWQCBCAGCEWCV-UHFFFAOYSA-N 0.000 description 1
PEMGGJDINLGTON-UHFFFAOYSA-N n-(3-aminophenyl)acetamide Chemical compound CC(=O)NC1=CC=CC(N)=C1 PEMGGJDINLGTON-UHFFFAOYSA-N 0.000 description 1
229920001778 nylon Polymers 0.000 description 1
125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 1
229920006122 polyamide resin Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
239000002964 rayon Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
235000017550 sodium carbonate Nutrition 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
238000003756 stirring Methods 0.000 description 1

JP1022884A 1984-01-25 1984-01-25 水溶性ジスアゾ化合物 Granted JPS60156759A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP1022884A JPS60156759A (ja)	1984-01-25	1984-01-25	水溶性ジスアゾ化合物

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP1022884A JPS60156759A (ja)	1984-01-25	1984-01-25	水溶性ジスアゾ化合物

Publications (2)

Publication Number	Publication Date
JPS60156759A JPS60156759A (ja)	1985-08-16
JPH0450944B2 true JPH0450944B2 (fr)	1992-08-17

Family

ID=11744420

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP1022884A Granted JPS60156759A (ja)	1984-01-25	1984-01-25	水溶性ジスアゾ化合物

Country Status (1)

Country	Link
JP (1)	JPS60156759A (fr)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0374655B1 (fr) *	1988-12-23	1993-09-15	Bayer Ag	Film ou feuille polarisant contenant des colorants de stilbène
US5272259A (en) *	1988-12-23	1993-12-21	Bayer Aktiengesellschaft	Stilbene dyestuffs and light-polarizing films or sheets containing stilbene
ES2104881T3 (es) *	1991-09-26	1997-10-16	Ciba Geigy Ag	Procedimiento para teñir papel con colorantes diazoicos.
US5423100A (en) *	1992-08-26	1995-06-13	Mitsui Toatsu Chemicals, Inc.	Water-soluble azo compounds and polarizing films using the compounds
US5639809A (en)	1994-06-22	1997-06-17	Mitsui Toatsu Chemicals, Inc.	Azo compounds and polarizing films using the compounds
WO2000037973A1 (fr) *	1998-12-18	2000-06-29	Nippon Kayaku Kabushiki Kaisha	Polariseur de couleur a support pour projecteur a cristaux liquides et projecteur associe
DE60020976T2 (de)	1999-07-14	2005-12-29	Nippon Kayaku K.K.	Farbstoff-polarisator
WO2004092282A1 (fr)	2003-04-16	2004-10-28	Nippon Kayaku Kabushiki Kaisha	Compose azoique et sel correspondant
CA2553415A1 (fr)	2004-02-04	2005-08-18	Nippon Kayaku Kabushiki Kaisha	Compose azoique et film polarisant et plaque polarisante le contenant
CA2586123A1 (fr)	2004-11-24	2006-06-01	Nippon Kayaku Kabushiki Kaisha	Composes azo et films ou plaques polarisant(e)s de type colorant les contenant
WO2007138980A1 (fr)	2006-06-01	2007-12-06	Nippon Kayaku Kabushiki Kaisha	Composé azo, sel et film polarisant contenant un colorant comprenant le composé ou son sel
CN101466798B (zh)	2006-06-13	2013-01-16	日本化药株式会社	偶氮化合物和包含它的染料偏振膜
CN101479347B (zh)	2006-06-22	2013-08-07	日本化药株式会社	偶氮化合物和含有该偶氮化合物的染料偏振膜
CN101688065B (zh) *	2007-07-09	2014-03-12	三菱化学株式会社	各向异性膜用化合物
TWI406907B (zh)	2007-11-02	2013-09-01	Nippon Kayaku Kk	偶氮化合物及含有彼等之染料系偏光膜
CN102037082B (zh)	2008-05-20	2014-05-28	日本化药株式会社	偶氮化合物及包含所述偶氮化合物的染料基偏振膜和偏振片
US8477268B2 (en)	2008-06-17	2013-07-02	Nippon Kayaku Kabushiki Kaisha	Azo compound and salts thereof, as well as dye-based polarization films and polarizing plates comprising the same
KR20140031861A (ko)	2011-05-30	2014-03-13	니폰 가야꾸 가부시끼가이샤	염료계 편광소자 및 편광판
US20140085721A1 (en)	2011-05-30	2014-03-27	Polatechno Co., Ltd.	Dye-Based Polarizing Element And Polarizing Plate
US20140126054A1 (en)	2011-05-31	2014-05-08	Polatechno Co., Ltd.	Dye-Based Polarizing Element And Polarizing Plate
JP6317334B2 (ja)	2013-04-03	2018-04-25	日本化薬株式会社	無彩色な染料系偏光素子、及び偏光板
TWI643908B (zh)	2013-04-03	2018-12-11	日本化藥公司	具有高透過率之無彩色之染料系偏光元件及偏光板
EP2983019A4 (fr)	2013-04-03	2016-11-02	Nippon Kayaku Kk	Élément polarisant achromatique, et plaque de polarisation
JP6064759B2 (ja) *	2013-04-12	2017-01-25	三菱化学株式会社	異方性色素膜用色素、該色素を含む組成物、異方性色素膜及び偏光素子
WO2016186183A1 (fr)	2015-05-20	2016-11-24	日本化薬株式会社	Élément polarisant de type colorant, plaque polarisante et dispositif d'affichage à cristaux liquides l'utilisant
CN109154691B (zh)	2016-05-16	2020-05-12	日本宝来科技有限公司	偏振构件和具有该偏振构件的平视显示装置
JP7035018B2 (ja)	2017-03-31	2022-03-14	日本化薬株式会社	アゾ化合物又はその塩、並びにこれを含有する染料系偏光膜、染料系偏光板、及び液晶表示装置

1984
- 1984-01-25 JP JP1022884A patent/JPS60156759A/ja active Granted

Also Published As

Publication number	Publication date
JPS60156759A (ja)	1985-08-16

Legal Events

Date	Code	Title	Description
2004-01-25	EXPY	Cancellation because of completion of term

Publication	Publication Date	Title
JPH0450944B2 (fr)	1992-08-17
JP3205096B2 (ja)	2001-09-04	水溶性アゾ染料及び該染料を用いた偏光フィルム
JPH0312606A (ja)	1991-01-21	水溶性アゾ染料及びこれを含有する偏光膜
JP4078476B2 (ja)	2008-04-23	アゾ化合物又はその塩及びそれらを含有する染料系偏光膜
JP2001033627A (ja)	2001-02-09	染料系偏光膜
EP0727465B1 (fr)	1999-08-04	Composé azoique et film polarisant le contenant
EP0584962B1 (fr)	1999-02-03	Composés azoiques solubles dans l'eau et films polarisants qui les utilisent
JPH0261988B2 (fr)	1990-12-21
JP4815721B2 (ja)	2011-11-16	ポリアゾ化合物又はその塩及びそれらを含有する染料系偏光膜
EP0688830B1 (fr)	1998-11-18	Composés azoiques et films polarisant les utilisant
JPH0813932B2 (ja)	1996-02-14	水溶性アゾ染料及びこれを含有する偏光膜
JP3270536B2 (ja)	2002-04-02	水溶性アゾ染料及び該染料を用いた偏光フィルム
US3859271A (en)	1975-01-07	Reactive yellow ' -sulfatoethylsulfonyl phenylazo-4-(1-substituted phenyl-3-methyl-5-amino)-pyrazole dyes
JP3617540B2 (ja)	2005-02-09	アゾ化合物及び該化合物を用いた偏光フィルム
JP2657416B2 (ja)	1997-09-24	偏光板
JPH05295282A (ja)	1993-11-09	水溶性アゾ染料及び該染料を用いた偏光フィルム
JPH09302250A (ja)	1997-11-25	アゾ化合物及びそれを含有する染料系偏光膜
EP0621317B1 (fr)	1998-12-16	Composé azoique et film polarisant le contenant
US4297278A (en)	1981-10-27	Pentakis-and heptakis-azoxy dyestuffs
JP3852966B2 (ja)	2006-12-06	アゾ化合物及び該化合物を用いた偏光フィルム
JP3803394B2 (ja)	2006-08-02	アゾ化合物及び該化合物を用いた偏光フィルム
JP3263121B2 (ja)	2002-03-04	水溶性アゾ染料及び該染料を用いた偏光フィルム
JP2001002631A (ja)	2001-01-09	ジスアゾ化合物及びそれを含有する染料系偏光膜
JP2003301120A (ja)	2003-10-21	新規なアゾ染料
US2420630A (en)	1947-05-13	Disazo dye compounds