CH363323A - Verwendung von 2,6-Dichlor-ms-dioxy-chromonoxanthonen als Pigmentfarbstoffe für den Textildruck - Google Patents
Verwendung von 2,6-Dichlor-ms-dioxy-chromonoxanthonen als Pigmentfarbstoffe für den TextildruckInfo
- Publication number
- CH363323A CH363323A CH858060A CH858060A CH363323A CH 363323 A CH363323 A CH 363323A CH 858060 A CH858060 A CH 858060A CH 858060 A CH858060 A CH 858060A CH 363323 A CH363323 A CH 363323A
- Authority
- CH
- Switzerland
- Prior art keywords
- dyes
- parts
- dichloro
- textile printing
- chromonoxanthones
- Prior art date
Links
- 239000000975 dye Substances 0.000 title claims description 26
- 239000000049 pigment Substances 0.000 title claims description 15
- 239000004753 textile Substances 0.000 title claims description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 238000000227 grinding Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- JCUBOZLXXVCRNO-UHFFFAOYSA-N 2,5-dichloro-3,6-dioxocyclohexa-1,4-diene-1,4-dicarboxylic acid Chemical class ClC=1C(C(=C(C(C1C(=O)O)=O)Cl)C(=O)O)=O JCUBOZLXXVCRNO-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 238000005684 Liebig rearrangement reaction Methods 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 150000001987 diarylethers Chemical class 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 235000002864 food coloring agent Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- -1 polypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 229940005657 pyrophosphoric acid Drugs 0.000 description 1
- 239000001054 red pigment Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- KBAFDSIZQYCDPK-UHFFFAOYSA-M sodium;octadecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCCCCCCCS([O-])(=O)=O KBAFDSIZQYCDPK-UHFFFAOYSA-M 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0041—Optical brightening agents, organic pigments
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB54506A DE1157325B (de) | 1959-08-22 | 1959-08-22 | Die Verwendung von 2, 6-Dichlor- und 2, 4, 6, 8-Tetrachlor-9, 10-dihydroxychromonoxanthon als Pigmente |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CH858060A4 CH858060A4 (enrdf_load_html_response) | 1962-02-15 |
| CH363323A true CH363323A (de) | 1962-09-14 |
Family
ID=6970634
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH858060A CH363323A (de) | 1959-08-22 | 1960-07-27 | Verwendung von 2,6-Dichlor-ms-dioxy-chromonoxanthonen als Pigmentfarbstoffe für den Textildruck |
| CH588661A CH420443A (de) | 1959-08-22 | 1960-07-27 | Verwendung von 2,6-Dichlor-ms-dioxy-chromonoxanthonen als Pigmentfarbstoffe |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH588661A CH420443A (de) | 1959-08-22 | 1960-07-27 | Verwendung von 2,6-Dichlor-ms-dioxy-chromonoxanthonen als Pigmentfarbstoffe |
Country Status (3)
| Country | Link |
|---|---|
| CH (2) | CH363323A (enrdf_load_html_response) |
| DE (1) | DE1157325B (enrdf_load_html_response) |
| GB (1) | GB920851A (enrdf_load_html_response) |
-
1959
- 1959-08-22 DE DEB54506A patent/DE1157325B/de active Pending
-
1960
- 1960-07-27 CH CH858060A patent/CH363323A/de unknown
- 1960-07-27 CH CH588661A patent/CH420443A/de unknown
- 1960-08-18 GB GB2861160D patent/GB920851A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| CH858060A4 (enrdf_load_html_response) | 1962-02-15 |
| CH420443A (de) | 1966-09-15 |
| GB920851A (en) | 1963-03-13 |
| DE1157325B (de) | 1963-11-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2856222C3 (de) | Wäßrige Farbstoffpräparate von in Wasser schwerlöslichen Farbstoffen, deren Herstellung und Verwendung | |
| DE2757982C2 (de) | Verbindungen der Isoindolinreihe und Verfahren zur Herstellung von in den anwendungstechnischen Eigenschaften verbesserten Pigmenten | |
| DE3142609A1 (de) | Marineblaue dispersionsfarbstoffmischungen | |
| DE3101885A1 (de) | Perylen-3,4,9,10-tetracarbonsaeurediimid- farbstoff | |
| CH363323A (de) | Verwendung von 2,6-Dichlor-ms-dioxy-chromonoxanthonen als Pigmentfarbstoffe für den Textildruck | |
| DE949309C (de) | Verfahren zur Herstellung von gefaerbtem Polyvinylharzpulver | |
| DE1150046B (de) | Verfahren zur Umwandlung der Kristallstruktur von linearem Rohchinacridon in die reine ª‰-Kristallphase | |
| DE637937C (de) | Verfahren zur Herstellung von Kuepenfarbstoffen der Anthrachinonreihe | |
| DE1544586C3 (de) | Anthrachinon-monoazofarbstoff-Pigmente, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| DE630219C (de) | Verfahren zur Herstellung von quartaeren Ammoniumverbindungen von Abkoemmlingen der Anthracenreihe | |
| DE1644244C (de) | Monoazopigmentfarbstoff, Verfahren zu dessen Herstellung und dessen Verwendung | |
| DE291983C (enrdf_load_html_response) | ||
| AT224781B (de) | Verfahren zur Herstellung neuer gemischter 1:2-Metallkomplexazofarbstoffe | |
| DE1285648B (de) | Verfahren zur Herstellung von Metallkomplexverbindungen | |
| DE723293C (de) | Verfahren zur Herstellung von Kuepenfarbstoffen | |
| DE1120043B (de) | Verfahren zur Umwandlung eines Kobaltphthalocyanins in einen Kuepenfarbstoff mit verbesserter Loeslichkeit in der Kuepe | |
| DE493352C (de) | Verfahren zur Herstellung von Farbstoffen | |
| DE2528063C2 (de) | Stabile, flüssige, wasserhaltige Färbezubereitungen, die Dispersionsund Reaktivfarbstoffe enthalten | |
| DE1444278A1 (de) | Verfahren zum Faerben von Fasermaterialien | |
| DE1544343C3 (de) | Benzthiazolylazonaphtholfarbstoffe, Verfahren zu deren Herstellung und Verwendung | |
| AT159419B (de) | Verfahren zur Herstellung metallhaltiger Farbstoffe. | |
| AT150610B (de) | Verfahren zur Herstellung von wasserunlöslichen Indulinen. | |
| DE663549C (de) | Verfahren zur Herstellung von Azofarbstoffen | |
| DE3422757A1 (de) | Perylen-3,4,9,10-tetracarbonsaeurediimid-farbstoff | |
| AT224778B (de) | Verfahren zur Herstellung neuer 1:2-Chromkomplexfarbstoffe |