KR980002165A - 반응성 알루미늄 프탈로시아닌 염료, 그의 제조방법 및 그의 용도 - Google Patents
반응성 알루미늄 프탈로시아닌 염료, 그의 제조방법 및 그의 용도 Download PDFInfo
- Publication number
- KR980002165A KR980002165A KR1019970025302A KR19970025302A KR980002165A KR 980002165 A KR980002165 A KR 980002165A KR 1019970025302 A KR1019970025302 A KR 1019970025302A KR 19970025302 A KR19970025302 A KR 19970025302A KR 980002165 A KR980002165 A KR 980002165A
- Authority
- KR
- South Korea
- Prior art keywords
- formula
- compound
- alkyl
- hydrogen
- group
- 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- Withdrawn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
- HUVXQFBFIFIDDU-UHFFFAOYSA-N aluminum phthalocyanine Chemical compound [Al+3].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 HUVXQFBFIFIDDU-UHFFFAOYSA-N 0.000 title claims 6
- 238000002360 preparation method Methods 0.000 title claims 5
- 239000001007 phthalocyanine dye Substances 0.000 title 1
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 12
- 239000001257 hydrogen Substances 0.000 claims abstract 12
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract 9
- 229920002554 vinyl polymer Polymers 0.000 claims abstract 9
- -1 sulfo, hydroxyl Chemical group 0.000 claims abstract 8
- 239000000126 substance Substances 0.000 claims abstract 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical class [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 4
- 229920006395 saturated elastomer Polymers 0.000 claims abstract 4
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract 3
- 150000001340 alkali metals Chemical class 0.000 claims abstract 3
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims abstract 3
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims abstract 2
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052782 aluminium Inorganic materials 0.000 claims abstract 2
- 239000004411 aluminium Substances 0.000 claims abstract 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims abstract 2
- 125000005842 heteroatom Chemical group 0.000 claims abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 2
- 125000001424 substituent group Chemical group 0.000 claims abstract 2
- 150000001875 compounds Chemical class 0.000 claims 29
- 239000000460 chlorine Substances 0.000 claims 8
- 150000003254 radicals Chemical class 0.000 claims 8
- 150000002431 hydrogen Chemical group 0.000 claims 6
- 238000000034 method Methods 0.000 claims 4
- 150000001412 amines Chemical class 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 2
- 239000007795 chemical reaction product Substances 0.000 claims 2
- 239000003638 chemical reducing agent Substances 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000047 product Substances 0.000 claims 2
- 239000011734 sodium Chemical group 0.000 claims 2
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 claims 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims 2
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 claims 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims 1
- FXKMTSIKHBYZSZ-UHFFFAOYSA-N 2-chloroethanesulfonic acid Chemical compound OS(=O)(=O)CCCl FXKMTSIKHBYZSZ-UHFFFAOYSA-N 0.000 claims 1
- 229920003043 Cellulose fiber Polymers 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical group [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims 1
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- URRHWTYOQNLUKY-UHFFFAOYSA-N [AlH3].[P] Chemical compound [AlH3].[P] URRHWTYOQNLUKY-UHFFFAOYSA-N 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000005392 carboxamide group Chemical group NC(=O)* 0.000 claims 1
- 238000005660 chlorination reaction Methods 0.000 claims 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 150000001923 cyclic compounds Chemical class 0.000 claims 1
- 238000004043 dyeing Methods 0.000 claims 1
- 239000002657 fibrous material Substances 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 229910052744 lithium Inorganic materials 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011591 potassium Chemical group 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- IWOKCMBOJXYDEE-UHFFFAOYSA-N sulfinylmethane Chemical compound C=S=O IWOKCMBOJXYDEE-UHFFFAOYSA-N 0.000 claims 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 claims 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 claims 1
- 125000004306 triazinyl group Chemical group 0.000 claims 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 claims 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 239000000985 reactive dye Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
- C09B62/503—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an esterified or non-esterified hydroxyalkyl sulfonyl or mercaptoalkyl sulfonyl group, a quaternised or non-quaternised aminoalkyl sulfonyl group, a heterylmercapto alkyl sulfonyl group, a vinyl sulfonyl or a substituted vinyl sulfonyl group, or a thiophene-dioxide group
- C09B62/517—Porphines; Azaporphines
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/002—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the linkage of the reactive group being alternatively specified
- C09B62/016—Porphines; Azaporphines
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
- C09B62/4401—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring with two or more reactive groups at least one of them being directly attached to a heterocyclic system and at least one of them being directly attached to a non-heterocyclic system
- C09B62/4403—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring with two or more reactive groups at least one of them being directly attached to a heterocyclic system and at least one of them being directly attached to a non-heterocyclic system the heterocyclic system being a triazine ring
- C09B62/4418—Porphines; Azoporphines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Paper (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19624469A DE19624469A1 (de) | 1996-06-19 | 1996-06-19 | Reaktive Aluminiumphthalocyaninfarbstoffe, Verfahren zu ihrer Herstellung und Verwendung |
| DE19624469.2 | 1996-06-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR980002165A true KR980002165A (ko) | 1998-03-30 |
Family
ID=7797383
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019970025302A Withdrawn KR980002165A (ko) | 1996-06-19 | 1997-06-18 | 반응성 알루미늄 프탈로시아닌 염료, 그의 제조방법 및 그의 용도 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US5856472A (enExample) |
| EP (1) | EP0814131B1 (enExample) |
| JP (1) | JPH10273604A (enExample) |
| KR (1) | KR980002165A (enExample) |
| BR (1) | BR9703630A (enExample) |
| CZ (1) | CZ191197A3 (enExample) |
| DE (2) | DE19624469A1 (enExample) |
| IN (1) | IN192323B (enExample) |
| TR (1) | TR199700513A2 (enExample) |
| TW (1) | TW455617B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9331841B2 (en) | 2013-05-21 | 2016-05-03 | Korea Research Institute Of Standards And Science | Data synchronization apparatus |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19937328B4 (de) * | 1998-08-11 | 2016-09-22 | Gottlieb Binder Gmbh & Co | Verwendung von Reaktivfarbstoffen |
| DE19964296B4 (de) * | 1998-08-11 | 2007-08-30 | Gottlieb Binder Gmbh & Co | Verwendung von Reaktivfarbstoffen |
| US6730780B2 (en) | 2000-02-21 | 2004-05-04 | Kao Corporation | Water-based ink |
| CN103694741B (zh) * | 2013-12-24 | 2014-12-31 | 丽源(湖北)科技有限公司 | 一种绿色活性染料混合物及其制备和应用 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE644252A (enExample) * | 1963-02-23 | |||
| IN150949B (enExample) * | 1978-06-02 | 1983-01-29 | Hoechst Ag | |
| DE3025790A1 (de) * | 1980-07-08 | 1982-02-04 | Hoechst Ag, 6000 Frankfurt | Wasserloesliche phthalocyaninverbindungen, verfahren zu ihrer herstellung und ihre verwendung als farbstoffe |
| DE3603124A1 (de) * | 1986-02-01 | 1987-08-06 | Hoechst Ag | Verfahren zur herstellung von wasserloeslichen phthalocyaninfarbstoffen |
| DE4226045A1 (de) * | 1992-08-06 | 1994-02-10 | Bayer Ag | Phthalocyaninreaktivfarbstoffe |
| DE4238047A1 (de) * | 1992-11-11 | 1994-05-19 | Basf Ag | Verfahren zur Herstellung von Phthalocyaninreaktivfarbstoffen |
| DE4340160A1 (de) * | 1993-10-15 | 1995-04-20 | Hoechst Ag | Wasserlösliche, metallfreie Phthalocyaninfarbstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE4338853A1 (de) * | 1993-11-13 | 1995-05-18 | Hoechst Ag | Wasserlösliche schwermetallfreie Phthalocyaninfarbstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung |
| GB2286403B (en) * | 1994-02-12 | 1998-09-16 | Sandoz Ltd | Solvent dyes |
| DE19521056A1 (de) * | 1994-06-15 | 1995-12-21 | Sandoz Ag | Aluminium Phthalocyanin Reaktivfarbstoffe |
| CH690649A5 (de) * | 1995-06-07 | 2000-11-30 | Clariant Finance Bvi Ltd | Phthalocyanin-Reaktivfarbstoffe für Fasern. |
| DE19529853A1 (de) * | 1995-08-14 | 1997-02-20 | Bayer Ag | Aluminium-Phthalocyanin-Reaktivfarbstoffe |
-
1996
- 1996-06-19 DE DE19624469A patent/DE19624469A1/de not_active Withdrawn
-
1997
- 1997-05-30 IN IN1010CA1997 patent/IN192323B/en unknown
- 1997-06-10 EP EP97109377A patent/EP0814131B1/de not_active Expired - Lifetime
- 1997-06-10 DE DE59701295T patent/DE59701295D1/de not_active Expired - Fee Related
- 1997-06-16 US US08/874,462 patent/US5856472A/en not_active Expired - Fee Related
- 1997-06-17 TR TR97/00513A patent/TR199700513A2/xx unknown
- 1997-06-17 TW TW086108447A patent/TW455617B/zh not_active IP Right Cessation
- 1997-06-18 KR KR1019970025302A patent/KR980002165A/ko not_active Withdrawn
- 1997-06-18 CZ CZ971911A patent/CZ191197A3/cs unknown
- 1997-06-18 JP JP9161650A patent/JPH10273604A/ja not_active Withdrawn
- 1997-06-19 BR BR9703630A patent/BR9703630A/pt not_active Application Discontinuation
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9331841B2 (en) | 2013-05-21 | 2016-05-03 | Korea Research Institute Of Standards And Science | Data synchronization apparatus |
Also Published As
| Publication number | Publication date |
|---|---|
| IN192323B (enExample) | 2004-04-10 |
| TW455617B (en) | 2001-09-21 |
| CZ191197A3 (cs) | 1998-06-17 |
| TR199700513A2 (xx) | 1998-01-21 |
| EP0814131B1 (de) | 2000-03-22 |
| DE59701295D1 (de) | 2000-04-27 |
| DE19624469A1 (de) | 1998-01-02 |
| US5856472A (en) | 1999-01-05 |
| JPH10273604A (ja) | 1998-10-13 |
| EP0814131A1 (de) | 1997-12-29 |
| BR9703630A (pt) | 1998-11-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP3649749B2 (ja) | 水溶性モノアゾ色素 | |
| KR980002165A (ko) | 반응성 알루미늄 프탈로시아닌 염료, 그의 제조방법 및 그의 용도 | |
| KR950008627A (ko) | 섬유-반응성 염료의 혼합물 및 섬유 물질을 염색하기 위한 그의 용도 | |
| KR930008074A (ko) | 수용성 섬유 - 반응성 염료, 그의 제조방법 및 그의 용도 | |
| CN1071361C (zh) | 纤维活性染料 | |
| KR860004114A (ko) | 음이온 염료의 리튬염을 제조하는 방법 | |
| KR930013007A (ko) | 수용성 섬유-반응성 염료, 그의 제조방법 및 그의 용도 | |
| KR970027222A (ko) | 반응성 염료, 이의 제조방법 및 이의 용도 | |
| KR870007989A (ko) | 수용성 프탈로시아닌 염료의 제조방법 | |
| JPH09165526A5 (enExample) | ||
| EP0356931A2 (en) | Anthrapyridone compounds having vinylsulfone type fiber reactive group through triazinyl bridging group | |
| KR880009974A (ko) | 구리 착염 포르마잔 화합물, 이의 제조방법, 염료로서 이의 용도 | |
| CA2435128A1 (en) | Fiber-reactive mono-azo dyes | |
| KR830006389A (ko) | 수가용성 프탈로시아닌 화합물의 제조방법 | |
| JP2009228007A (ja) | ビスアゾ化合物及びそれを用いる繊維材料の染色又は捺染方法 | |
| KR890010123A (ko) | 수용성 디스아조 화합물, 이의 제조방법 및 염료로서의 이의 용도 | |
| KR930006118A (ko) | 수용성 섬유 반응성 염료의 혼합물 및 그의 용도 | |
| JPH08511576A (ja) | 繊維反応性アントラキノン染料 | |
| KR950014230A (ko) | 수용성 프탈로시아닌 염료, 그 제조방법 및 용도 | |
| JPH09195181A (ja) | 混紡品の染色または捺染法 | |
| JP3576187B2 (ja) | 染料混合物、それらの製造方法及びそれらの用途 | |
| KR900014534A (ko) | 수용성 섬유-반응성 염료, 이의 제조방법 및 이의 용도 | |
| KR960001063B1 (ko) | 안트라퀴논 화합물, 그 제조방법 및 이를 사용한 섬유의 염색 또는 날염방법 | |
| KR970010888A (ko) | 알루미늄 프탈로시아닌 반응성 염료 | |
| KR950032485A (ko) | 신규반응성 염료, 그의 제조 방법 및 그의 용도 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19970618 |
|
| PG1501 | Laying open of application | ||
| PC1203 | Withdrawal of no request for examination | ||
| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |