CH653048A5 - Azo-pigmentfarbstoffe. - Google Patents
Azo-pigmentfarbstoffe. Download PDFInfo
- Publication number
- CH653048A5 CH653048A5 CH4923/82A CH492382A CH653048A5 CH 653048 A5 CH653048 A5 CH 653048A5 CH 4923/82 A CH4923/82 A CH 4923/82A CH 492382 A CH492382 A CH 492382A CH 653048 A5 CH653048 A5 CH 653048A5
- Authority
- CH
- Switzerland
- Prior art keywords
- parts
- chs
- formula
- hydrogen
- pigment
- Prior art date
Links
- 239000000049 pigment Substances 0.000 title description 18
- 239000000975 dye Substances 0.000 title description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 35
- 239000000460 chlorine Substances 0.000 description 18
- 229910052739 hydrogen Inorganic materials 0.000 description 14
- 239000001257 hydrogen Substances 0.000 description 14
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 229910052801 chlorine Inorganic materials 0.000 description 9
- 150000002431 hydrogen Chemical group 0.000 description 9
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 9
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 230000008878 coupling Effects 0.000 description 4
- 238000010168 coupling process Methods 0.000 description 4
- 238000005859 coupling reaction Methods 0.000 description 4
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- GLLRIXZGBQOFLM-UHFFFAOYSA-N Xanthorin Natural products C1=C(C)C=C2C(=O)C3=C(O)C(OC)=CC(O)=C3C(=O)C2=C1O GLLRIXZGBQOFLM-UHFFFAOYSA-N 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- 239000012954 diazonium Substances 0.000 description 2
- 150000001989 diazonium salts Chemical class 0.000 description 2
- QKIUAMUSENSFQQ-UHFFFAOYSA-N dimethylazanide Chemical compound C[N-]C QKIUAMUSENSFQQ-UHFFFAOYSA-N 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical group COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- 229940093475 2-ethoxyethanol Drugs 0.000 description 1
- ALKYHXVLJMQRLQ-UHFFFAOYSA-N 3-Hydroxy-2-naphthoate Chemical compound C1=CC=C2C=C(O)C(C(=O)O)=CC2=C1 ALKYHXVLJMQRLQ-UHFFFAOYSA-N 0.000 description 1
- OALYTRUKMRCXNH-UHFFFAOYSA-N 5-pentyloxolan-2-one Chemical compound CCCCCC1CCC(=O)O1 OALYTRUKMRCXNH-UHFFFAOYSA-N 0.000 description 1
- -1 Ci-s-alkyl Chemical group 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000001054 red pigment Substances 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/18—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides
- C09B29/20—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides of the naphthalene series
-
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/0003—Monoazo dyes prepared by diazotising and coupling from diazotized anilines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Coloring (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3134126 | 1981-08-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH653048A5 true CH653048A5 (de) | 1985-12-13 |
Family
ID=6140364
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH4923/82A CH653048A5 (de) | 1981-08-28 | 1982-08-17 | Azo-pigmentfarbstoffe. |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US4623397A (en]) |
| JP (1) | JPS5842658A (en]) |
| CH (1) | CH653048A5 (en]) |
| FR (1) | FR2512042B1 (en]) |
| GB (1) | GB2104911B (en]) |
| HK (1) | HK29986A (en]) |
| IT (1) | IT1186697B (en]) |
| KE (1) | KE3613A (en]) |
| MY (1) | MY8600532A (en]) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102007028871A1 (de) | 2007-06-22 | 2008-12-24 | Clariant International Limited | Verfahren zur Herstellung von reinem C.I. Pigment Orange 74 |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0104240D0 (en) * | 2001-02-21 | 2001-04-11 | Clariant Int Ltd | Copolymer composition having pigment like properties |
| JP5134794B2 (ja) * | 2006-08-22 | 2013-01-30 | 東京色材工業株式会社 | 変異原性の低減されたナフトール系アゾ顔料組成物およびその製造方法 |
| JP7158957B2 (ja) * | 2018-08-30 | 2022-10-24 | 保土谷化学工業株式会社 | アゾ化合物を含有する着色組成物、カラーフィルター用着色剤およびカラーフィルター |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1927115A (en) * | 1931-11-13 | 1933-09-19 | Gen Aniline Works Inc | Water-insoluble mono-azodyestuff and fiber dyed therewith |
| FR768931A (fr) * | 1933-03-01 | 1934-08-16 | Ig Farbenindustrie Ag | Production de nouveaux colorants azoïques insolubles à l'eau |
| US2066986A (en) * | 1933-03-01 | 1937-01-05 | Gen Aniline Works Inc | Water-insoluble azodyestuffs |
| US2004383A (en) * | 1933-08-12 | 1935-06-11 | Gen Aniline Works Inc | Azo-dyestuff and fiber dyed therewith |
| FR777163A (fr) * | 1933-08-12 | 1935-02-13 | Ig Farbenindustrie Ag | Colorant azoïque et son procédé de fabrication |
| US2209749A (en) * | 1937-05-22 | 1940-07-30 | Gen Aniline & Film Corp | Water-insoluble azo dyestuffs |
| FR838200A (fr) * | 1937-05-22 | 1939-02-28 | Ig Farbenindustrie Ag | Colorants azoïques insolubles dans l'eau et procédé pour préparer ces colorants en substance ou sur la fibre |
| GB496735A (en) * | 1937-06-04 | 1938-12-05 | Ig Farbenindustrie Ag | Process for the manufacture of water-insoluble azo-dyestuffs in substance or on the fibre |
| DE700160C (de) * | 1938-02-24 | 1940-12-14 | I G Farbenindustrie Akt Ges | Verfahren zur Herstellung von Monoazofarbstoffen |
| FR858782A (fr) * | 1938-08-06 | 1940-12-03 | Ig Farbenindustrie Ag | Colorants azoïques insolubles dans l'eau, fibres végétales colorées par ceux-ci et procédés de préparation de ces divers produits |
| DE724831C (de) * | 1939-04-02 | 1942-09-08 | Ig Farbenindustrie Ag | Verfahren zur Herstellung von wasserunloeslichen Monoazofarbstoffen |
| IT500247A (en]) * | 1951-08-31 | |||
| GB897484A (en) * | 1959-08-24 | 1962-05-30 | Ici Ltd | New insoluble monoazo colouring matters containing isopropylsulphamyl groups |
| DE1225321B (de) * | 1961-12-29 | 1966-09-22 | Hoechst Ag | Verfahren zur Herstellung von wasserunloeslichen Monoazofarbstoffen |
| CH452749A (de) * | 1967-01-27 | 1968-03-15 | Ciba Geigy | Verfahren zur Herstellung neuer Azofarbstoffpigmente |
| CH498877A (de) * | 1967-11-10 | 1970-11-15 | Ciba Geigy | Verfahren zur Herstellung transparent gefärbter Formkörper auf Basis regenerierter Cellulose mit organischen schwerlöslichen Farbstoffen |
| FR2034105A1 (en) * | 1969-02-04 | 1970-12-11 | Wolfen Filmfab Veb | Preparation of azo pigments |
| CH509384A (de) * | 1969-02-18 | 1971-06-30 | Sandoz Ag | Verfahren zur Herstellung von Azoverbindungen |
| JPS5516573B2 (en]) * | 1972-11-16 | 1980-05-02 | ||
| CH619584GA3 (en]) * | 1975-03-26 | 1980-10-15 | ||
| DE2716934A1 (de) * | 1977-04-16 | 1978-10-26 | Basf Ag | Farbstoffzubereitungen zum faerben von cellulose und cellulosehaltigem textilmaterial sowie neue farbstoffe |
| DE2916484A1 (de) * | 1979-04-24 | 1980-11-06 | Bayer Ag | Verfahren zum faerben und bedrucken von cellulosefasern |
-
1982
- 1982-08-17 CH CH4923/82A patent/CH653048A5/de not_active IP Right Cessation
- 1982-08-17 FR FR8214313A patent/FR2512042B1/fr not_active Expired
- 1982-08-25 GB GB08224349A patent/GB2104911B/en not_active Expired
- 1982-08-26 IT IT49036/82A patent/IT1186697B/it active
- 1982-08-26 JP JP57147010A patent/JPS5842658A/ja active Granted
-
1984
- 1984-10-10 US US06/659,246 patent/US4623397A/en not_active Expired - Lifetime
-
1986
- 1986-03-06 KE KE3613A patent/KE3613A/xx unknown
- 1986-04-24 HK HK299/86A patent/HK29986A/xx not_active IP Right Cessation
- 1986-12-30 MY MY532/86A patent/MY8600532A/xx unknown
-
1987
- 1987-02-19 US US07/016,300 patent/US4879373A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102007028871A1 (de) | 2007-06-22 | 2008-12-24 | Clariant International Limited | Verfahren zur Herstellung von reinem C.I. Pigment Orange 74 |
| WO2009000375A3 (de) * | 2007-06-22 | 2009-05-28 | Clariant Finance Bvi Ltd | Verfahren zur herstellung von reinem c.i. pigment orange 74 |
| US8329369B2 (en) | 2007-06-22 | 2012-12-11 | Clariant Finance (Bvi) Limited | Method for the production of pure C.I. pigment orange 74 |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2104911A (en) | 1983-03-16 |
| US4623397A (en) | 1986-11-18 |
| KE3613A (en) | 1986-03-27 |
| GB2104911B (en) | 1985-04-17 |
| JPS5842658A (ja) | 1983-03-12 |
| HK29986A (en) | 1986-05-02 |
| IT8249036A0 (it) | 1982-08-26 |
| FR2512042B1 (fr) | 1986-12-05 |
| US4879373A (en) | 1989-11-07 |
| MY8600532A (en) | 1986-12-31 |
| FR2512042A1 (fr) | 1983-03-04 |
| JPH0413387B2 (en]) | 1992-03-09 |
| IT1186697B (it) | 1987-12-04 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| NV | New agent |
Representative=s name: SANDOZ TECHNOLOGIE AG |
|
| PUE | Assignment |
Owner name: SANDOZ AG TRANSFER- CLARIANT FINANCE (BVI) LIMITED |
|
| NV | New agent |
Representative=s name: CLARIANT INTERNATIONAL LTD. |
|
| PL | Patent ceased |