CH625537A5 - - Google Patents
Download PDFInfo
- Publication number
- CH625537A5 CH625537A5 CH729777A CH729777A CH625537A5 CH 625537 A5 CH625537 A5 CH 625537A5 CH 729777 A CH729777 A CH 729777A CH 729777 A CH729777 A CH 729777A CH 625537 A5 CH625537 A5 CH 625537A5
- Authority
- CH
- Switzerland
- Prior art keywords
- atoms
- benzoylamino
- dyeing
- formula
- polyesters
- Prior art date
Links
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 15
- -1 anthraquinone compound Chemical class 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 10
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 238000004043 dyeing Methods 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 229920000728 polyester Polymers 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 239000011368 organic material Substances 0.000 claims description 4
- 239000000020 Nitrocellulose Substances 0.000 claims description 2
- 229920002678 cellulose Polymers 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 229920001220 nitrocellulos Polymers 0.000 claims description 2
- 229920000098 polyolefin Polymers 0.000 claims description 2
- 229920002635 polyurethane Polymers 0.000 claims description 2
- 239000004814 polyurethane Substances 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
- 229940081735 acetylcellulose Drugs 0.000 claims 1
- 239000001913 cellulose Substances 0.000 claims 1
- 229920002301 cellulose acetate Polymers 0.000 claims 1
- 238000004040 coloring Methods 0.000 claims 1
- 239000004922 lacquer Substances 0.000 claims 1
- 229920003023 plastic Polymers 0.000 claims 1
- 239000004033 plastic Substances 0.000 claims 1
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 11
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 2
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 2
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical class CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 2
- YZVJFFKAKLWXOE-UHFFFAOYSA-N 6-heptadecyl-1,3,5-triazine-2,4-diamine Chemical compound CCCCCCCCCCCCCCCCCC1=NC(N)=NC(N)=N1 YZVJFFKAKLWXOE-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- BOCJQSFSGAZAPQ-UHFFFAOYSA-N 1-chloroanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2Cl BOCJQSFSGAZAPQ-UHFFFAOYSA-N 0.000 description 1
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical class CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- NJYZCEFQAIUHSD-UHFFFAOYSA-N acetoguanamine Chemical class CC1=NC(N)=NC(N)=N1 NJYZCEFQAIUHSD-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- GBRBMTNGQBKBQE-UHFFFAOYSA-L copper;diiodide Chemical compound I[Cu]I GBRBMTNGQBKBQE-UHFFFAOYSA-L 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- 238000005108 dry cleaning Methods 0.000 description 1
- 238000007380 fibre production Methods 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 150000002537 isoquinolines Chemical class 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- RHSBIGNQEIPSCT-UHFFFAOYSA-N stearonitrile Chemical compound CCCCCCCCCCCCCCCCCC#N RHSBIGNQEIPSCT-UHFFFAOYSA-N 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Coloring (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH729777A CH625537A5 (en, 2012) | 1977-06-14 | 1977-06-14 | |
| US05/913,159 US4211688A (en) | 1977-06-14 | 1978-06-06 | Process for dyeing high-molecular organic material in the melt |
| DE19782825613 DE2825613A1 (de) | 1977-06-14 | 1978-06-12 | Verfahren zum faerben von hochmolekularem organischem material in der masse |
| CA305,245A CA1104305A (en) | 1977-06-14 | 1978-06-12 | Process for dyeing high-molecular organic material in the melt |
| IT7824511A IT7824511A0 (it) | 1977-06-14 | 1978-06-13 | Procedimento per la tintura di un materiale organico di elevato peso molecolare nella massa. |
| GB7826820A GB2000159B (en) | 1977-06-14 | 1978-06-13 | Process for dyeing high-molecular organic material in the melt |
| JP7201978A JPS546035A (en) | 1977-06-14 | 1978-06-14 | Method of dyeing high molecular organic material |
| FR7817768A FR2394572A1 (fr) | 1977-06-14 | 1978-06-14 | Procede pour teindre, dans la masse, des matieres organiques a haut poids moleculaire |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH729777A CH625537A5 (en, 2012) | 1977-06-14 | 1977-06-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH625537A5 true CH625537A5 (en, 2012) | 1981-09-30 |
Family
ID=4322921
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH729777A CH625537A5 (en, 2012) | 1977-06-14 | 1977-06-14 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4211688A (en, 2012) |
| JP (1) | JPS546035A (en, 2012) |
| CA (1) | CA1104305A (en, 2012) |
| CH (1) | CH625537A5 (en, 2012) |
| DE (1) | DE2825613A1 (en, 2012) |
| FR (1) | FR2394572A1 (en, 2012) |
| GB (1) | GB2000159B (en, 2012) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4725378A (en) * | 1982-03-22 | 1988-02-16 | The Dow Chemical Company | Systems for delayed release of bleaching agents |
| JPS60250052A (ja) * | 1984-05-28 | 1985-12-10 | Mitsubishi Chem Ind Ltd | 樹脂用着色材 |
| US6357527B1 (en) | 2000-05-05 | 2002-03-19 | Halliburton Energy Services, Inc. | Encapsulated breakers and method for use in treating subterranean formations |
| RU2580144C2 (ru) * | 2010-10-28 | 2016-04-10 | Тейджин Арамид Б.В. | Окрашенные в процессе формования арамидные волокна |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE551884C (de) * | 1930-02-20 | 1932-06-06 | Ig Farbenindustrie Ag | Verfahren zur Darstellung von Kuepenfarbstoffen der Anthrachinonreihe |
| DE553312C (de) * | 1930-06-04 | 1932-06-24 | Ig Farbenindustrie Ag | Verfahren zur Darstellung von Kuepenfarbstoffen der Anthrachinonreihe |
| BE567462A (en, 2012) * | 1957-05-08 | |||
| BE620471A (en, 2012) * | 1961-07-21 | |||
| GB950378A (en) * | 1962-02-14 | 1964-02-26 | Arthur Jack Sackville Evans | New anthraquinone dyestuffs and process for their manufacture |
| DE1274069B (de) * | 1963-09-25 | 1968-08-01 | Cassella Farbwerke Mainkur Ag | Verfahren zur Herstellung goldgelber Kuepenfarbstoffdrucke auf Cellulosetextilien |
| CH471852A (de) * | 1966-04-28 | 1969-04-30 | Ciba Geigy | Verfahren zum Färben organischer Erzeugnisse mit Pigmentfarbstoffen |
| US3839332A (en) * | 1967-08-18 | 1974-10-01 | Ciba Geigy Ag | Process for the manufacture of anthraquinone dyestuffs |
| US3642795A (en) * | 1968-02-19 | 1972-02-15 | Ciba Ltd | Triazinyl-anthraquinone dyestuffs |
| FR2128369A1 (en) * | 1971-03-03 | 1972-10-20 | Ciba Geigy Ag | Anthraquinone/acridone vat dyes - and pigments contg triazine grps for cellulosic fibres, plastics, paints, etc |
| CH580136A5 (en, 2012) * | 1973-01-30 | 1976-09-30 | Ciba Geigy Ag | |
| CH579613A5 (en, 2012) * | 1973-01-30 | 1976-09-15 | Ciba Geigy Ag | |
| GB1476687A (en) * | 1973-08-22 | 1977-06-16 | Ciba Geigy Ag | Vat dyes their manufacture and their use |
-
1977
- 1977-06-14 CH CH729777A patent/CH625537A5/de not_active IP Right Cessation
-
1978
- 1978-06-06 US US05/913,159 patent/US4211688A/en not_active Expired - Lifetime
- 1978-06-12 DE DE19782825613 patent/DE2825613A1/de not_active Withdrawn
- 1978-06-12 CA CA305,245A patent/CA1104305A/en not_active Expired
- 1978-06-13 GB GB7826820A patent/GB2000159B/en not_active Expired
- 1978-06-14 FR FR7817768A patent/FR2394572A1/fr active Granted
- 1978-06-14 JP JP7201978A patent/JPS546035A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| FR2394572A1 (fr) | 1979-01-12 |
| GB2000159B (en) | 1982-01-27 |
| GB2000159A (en) | 1979-01-04 |
| US4211688A (en) | 1980-07-08 |
| JPS546035A (en) | 1979-01-17 |
| DE2825613A1 (de) | 1979-01-04 |
| CA1104305A (en) | 1981-07-07 |
| FR2394572B1 (en, 2012) | 1980-06-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1695090A1 (de) | Praktisch farblose, uv-licht absorbierende verbindungen, sowie verfahren zu deren herstellung | |
| DE2121013A1 (de) | Quaternäre Ammoniumverbindungen | |
| CH625537A5 (en, 2012) | ||
| DE1298074B (de) | Optische Aufhellmittel | |
| DE1142212B (de) | Verfahren zur Herstellung von sulfonsaeuregruppenfreien Dioxazinfarbstoffen | |
| DE1294917B (de) | Optisches Aufhellmittel | |
| DE1444006C3 (de) | Verwendung von Azolyl-thiophenverbindungen als optische Aufhellmittel für organische Materialien | |
| DE2729369A1 (de) | Arylaminoanthrachinone, verfahren zu deren herstellung und deren verwendung | |
| DE1282214B (de) | Verfahren zur Herstellung von Farbstoffen der Phthaloperinonreihe | |
| DE1281385B (de) | Optische Aufheller | |
| DE1253222B (de) | Optische Aufhellmittel | |
| EP1293538B1 (de) | Verfahren zur Herstellung von Styrylfarbstoffen | |
| CH630938A5 (de) | Verfahren zum faerben von hochmolekularem organischem material. | |
| AT254838B (de) | Verfahren zur Herstellung modifizierter Polyolefinwachse | |
| DE1278983B (de) | Optische Aufhellmittel | |
| EP0020305B1 (de) | 1-Hydroxy-4-hetero-arylamino-anthrachinon-Farbstoffe, deren Herstellung und deren Verwendung beim Färben von Polyestern in der Masse | |
| DE2727776A1 (de) | Verfahren zum flammfestmachen von polyesterfasermaterialien mit substituierten sulfurylamiden | |
| AT286224B (de) | Aufhellungsmittel | |
| EP1329482B1 (de) | Verfahren zur Herstellung von Styrylverbindungen | |
| DE1298659B (de) | Verfahren zur Herstellung wasserunloeslicher Azofarbstoffe | |
| DE1569693A1 (de) | Verfahren zur Herstellung von Farbstoffen | |
| DE2159797A1 (de) | Styryltriazole, deren Verwendung zum optischen Aufhellen von organischen Materialien und Verfahren zu deren Herstellung | |
| CH523955A (de) | Verfahren zur Herstellung sulfonsäuregruppenfreier Azoverbindungen | |
| DE1569856C (de) | Farbstoffe der Naphthoylenbenzimid azolreihe, deren Herstellung und Verwen dung | |
| DE1594822C (de) | Optische Aufhellmittel |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased | ||
| PL | Patent ceased |