DE1795091C3 - 4-Methoxy-naphthalimid-derivate, Verfahren zu ihrer Herstellung und deren Verwendung - Google Patents
4-Methoxy-naphthalimid-derivate, Verfahren zu ihrer Herstellung und deren VerwendungInfo
- Publication number
- DE1795091C3 DE1795091C3 DE1795091A DE1795091A DE1795091C3 DE 1795091 C3 DE1795091 C3 DE 1795091C3 DE 1795091 A DE1795091 A DE 1795091A DE 1795091 A DE1795091 A DE 1795091A DE 1795091 C3 DE1795091 C3 DE 1795091C3
- Authority
- DE
- Germany
- Prior art keywords
- radical
- phenyl
- parts
- substituted
- methyl
- 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.)
- Expired
Links
- 238000000034 method Methods 0.000 title description 11
- 238000002360 preparation method Methods 0.000 title description 5
- XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical class C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 description 17
- 150000001875 compounds Chemical class 0.000 description 17
- -1 2,5- Dimethyl-l-pyrazolium radical Chemical class 0.000 description 14
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000000835 fiber Substances 0.000 description 11
- 230000003287 optical effect Effects 0.000 description 11
- 239000000203 mixture Substances 0.000 description 8
- 150000003254 radicals Chemical class 0.000 description 8
- 238000002844 melting Methods 0.000 description 7
- 230000008018 melting Effects 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 6
- 229920002239 polyacrylonitrile Polymers 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 5
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 description 4
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 238000005282 brightening Methods 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 238000009833 condensation Methods 0.000 description 4
- 230000005494 condensation Effects 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 4
- 125000004174 2-benzimidazolyl group Chemical group [H]N1C(*)=NC2=C([H])C([H])=C([H])C([H])=C12 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 150000003949 imides Chemical class 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000012022 methylating agents Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- FKUONVSFQBBRTR-UHFFFAOYSA-N (4-bromonaphthalene-1-carbonyl) 4-bromonaphthalene-1-carboxylate Chemical compound C12=CC=CC=C2C(Br)=CC=C1C(=O)OC(=O)C1=CC=C(Br)C2=CC=CC=C12 FKUONVSFQBBRTR-UHFFFAOYSA-N 0.000 description 2
- ZOICTXNECDDJFS-UHFFFAOYSA-N 2,4-dimethyl-3h-1,2,4-triazole Chemical compound CN1CN(C)N=C1 ZOICTXNECDDJFS-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- FIULGFJIHJJXMT-UHFFFAOYSA-N [C]1[N]C=CC=C1 Chemical compound [C]1[N]C=CC=C1 FIULGFJIHJJXMT-UHFFFAOYSA-N 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 235000005074 zinc chloride Nutrition 0.000 description 2
- 239000011592 zinc chloride Substances 0.000 description 2
- UHMDKSPUHZLVPG-UHFFFAOYSA-N (4-methoxynaphthalene-1-carbonyl) 4-methoxynaphthalene-1-carboxylate Chemical compound COC1=CC=C(C2=CC=CC=C12)C(=O)OC(=O)C1=CC=C(C2=CC=CC=C12)OC UHMDKSPUHZLVPG-UHFFFAOYSA-N 0.000 description 1
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
- JWAWEQBUZOGIBZ-UHFFFAOYSA-O 1-methyl-2h-triazol-1-ium Chemical compound C[N+]1=CC=NN1 JWAWEQBUZOGIBZ-UHFFFAOYSA-O 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical class C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 1
- LNVWRBNPXCUYJI-UHFFFAOYSA-N 3,5-dimethyl-1h-pyrazol-4-amine Chemical compound CC1=NNC(C)=C1N LNVWRBNPXCUYJI-UHFFFAOYSA-N 0.000 description 1
- QEHKQNYBBLCFIJ-UHFFFAOYSA-N 4-phenyl-1h-pyrazol-5-amine Chemical compound NC1=NNC=C1C1=CC=CC=C1 QEHKQNYBBLCFIJ-UHFFFAOYSA-N 0.000 description 1
- PXHOKIKYPZXSKW-UHFFFAOYSA-N 5-methyl-3-phenyl-1h-pyrazol-4-amine Chemical compound NC1=C(C)NN=C1C1=CC=CC=C1 PXHOKIKYPZXSKW-UHFFFAOYSA-N 0.000 description 1
- UMDNRKCXSUJMCY-UHFFFAOYSA-N 5-methyl-4-phenyl-1h-pyrazol-3-amine Chemical compound N1N=C(N)C(C=2C=CC=CC=2)=C1C UMDNRKCXSUJMCY-UHFFFAOYSA-N 0.000 description 1
- PWSZRRFDVPMZGM-UHFFFAOYSA-N 5-phenyl-1h-pyrazol-3-amine Chemical compound N1N=C(N)C=C1C1=CC=CC=C1 PWSZRRFDVPMZGM-UHFFFAOYSA-N 0.000 description 1
- CNUWYNDMLFVRBU-UHFFFAOYSA-N 6-methoxy-2-methylbenzo[de]isoquinoline-1,3-dione Chemical compound O=C1N(C)C(=O)C2=CC=CC3=C2C1=CC=C3OC CNUWYNDMLFVRBU-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 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
- 238000005684 Liebig rearrangement reaction Methods 0.000 description 1
- PQBAWAQIRZIWIV-UHFFFAOYSA-N N-methylpyridinium Chemical compound C[N+]1=CC=CC=C1 PQBAWAQIRZIWIV-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-N methyl sulfate Chemical class COS(O)(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000005956 quaternization reaction Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- UKLNMMHNWFDKNT-UHFFFAOYSA-M sodium chlorite Chemical compound [Na+].[O-]Cl=O UKLNMMHNWFDKNT-UHFFFAOYSA-M 0.000 description 1
- 229960002218 sodium chlorite Drugs 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
- C07D221/06—Ring systems of three rings
- C07D221/14—Aza-phenalenes, e.g. 1,8-naphthalimide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/60—Optical bleaching or brightening
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/92—Synthetic fiber dyeing
- Y10S8/927—Polyacrylonitrile fiber
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR117728A FR1541050A (fr) | 1967-08-11 | 1967-08-11 | Nouveaux agents de blanchiment optique, leur préparation et leurs applications |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE1795091A1 DE1795091A1 (de) | 1972-01-05 |
| DE1795091B2 DE1795091B2 (de) | 1977-11-10 |
| DE1795091C3 true DE1795091C3 (de) | 1978-06-22 |
Family
ID=8636807
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1795091A Expired DE1795091C3 (de) | 1967-08-11 | 1968-08-08 | 4-Methoxy-naphthalimid-derivate, Verfahren zu ihrer Herstellung und deren Verwendung |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3649633A (enExample) |
| BE (1) | BE718203A (enExample) |
| BR (1) | BR6801378D0 (enExample) |
| CH (1) | CH483429A (enExample) |
| DE (1) | DE1795091C3 (enExample) |
| FR (1) | FR1541050A (enExample) |
| GB (1) | GB1227239A (enExample) |
| NL (1) | NL143234B (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2186025A5 (enExample) * | 1972-05-24 | 1974-01-04 | Ugine Kuhlmann | |
| CH590965A5 (enExample) * | 1973-12-19 | 1977-08-31 | Ciba Geigy Ag | |
| DE2507459C3 (de) * | 1975-02-21 | 1979-11-15 | Basf Ag, 6700 Ludwigshafen | 4,5-Dialkoxy-N-cycloammoniumnaphthalimide |
| DE2944867A1 (de) * | 1979-11-07 | 1981-05-27 | Hoechst Ag, 6000 Frankfurt | Kationische verbindungen der naphthalimid-reihe, verfahren zu deren herstellung und deren verwendung |
-
1967
- 1967-08-11 FR FR117728A patent/FR1541050A/fr not_active Expired
-
1968
- 1968-07-09 CH CH1021568A patent/CH483429A/fr not_active IP Right Cessation
- 1968-07-17 BE BE718203D patent/BE718203A/xx unknown
- 1968-07-31 NL NL686810816A patent/NL143234B/xx not_active IP Right Cessation
- 1968-08-08 DE DE1795091A patent/DE1795091C3/de not_active Expired
- 1968-08-09 US US751349A patent/US3649633A/en not_active Expired - Lifetime
- 1968-08-12 GB GB1227239D patent/GB1227239A/en not_active Expired
- 1968-09-09 BR BR201378/68A patent/BR6801378D0/pt unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BR6801378D0 (pt) | 1973-02-20 |
| US3649633A (en) | 1972-03-14 |
| FR1541050A (fr) | 1968-10-04 |
| DE1795091A1 (de) | 1972-01-05 |
| DE1795091B2 (de) | 1977-11-10 |
| BE718203A (enExample) | 1969-01-17 |
| CH483429A (fr) | 1969-12-31 |
| NL6810816A (enExample) | 1969-02-13 |
| GB1227239A (enExample) | 1971-04-07 |
| NL143234B (nl) | 1974-09-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2915323C2 (enExample) | ||
| DE2262633C3 (de) | Sulfogruppen und v-Triazolylreste enthaltende 4,4'-Divinyldiphenyl-Verbindungen und deren Salze | |
| DE1619428A1 (de) | Verwendung von quaternaeren Methinverbindungen zum Faerben von Textilgut aus Faeden oder Fasern aus hydrophoben Polymeren | |
| EP0055224A2 (de) | Verfahren zum Spinnfärben von Polymeren oder Mischpolymeren des Acrylnitrils | |
| DE1795091C3 (de) | 4-Methoxy-naphthalimid-derivate, Verfahren zu ihrer Herstellung und deren Verwendung | |
| DE2020817A1 (de) | Optische Aufhellungsmittel auf der Basis von mit Heterocyclen substituierten Stilbenen | |
| DE1940065B2 (de) | Verfahren zur Verminderung der Viskosität von Polytrimellithamidimidlösungen | |
| DE2337845A1 (de) | Neue konjugierte aromatische verbindungen und ihre verwendung als optische aufheller | |
| DE1138318B (de) | Photographische Schichten fuer das Silberfarbbleichverfahren | |
| DE1794396C2 (de) | Aufhellungsmittel | |
| DE2159469C3 (de) | Quaternierte 2-(2-Benzofuranyl)-benzimidazole | |
| EP0011824A1 (de) | Benzofuranyl-benzimidazole, Verfahren zu ihrer Herstellung sowie ihre Verwendung zum optischen Aufhellen von organischen Materialien | |
| EP0061624A1 (de) | Kationische Farbstoffe und deren Verwendung | |
| DE1670908A1 (de) | Neue Benzimidazolverbindungen,Verfahren zu ihrer Herstellung und ihre Verwendung als optische Aufhellungsmittel | |
| DE1670873B2 (de) | Pyrazolyl-triazolyl-cumarine | |
| EP0005465A1 (de) | Benzofuranyl-benzimidazole, Verfahren zu ihrer Herstellung sowie ihre Verwendung zum optischen Aufhellen von organischen Materialien | |
| DE1695524C3 (de) | 4-(2-Naphtho [a] triazolyl) - zimtsäurederivate, Verfahren zu deren Herstellung und deren Verwendung als optische Aufheller für organische Materialien | |
| DE1670999B2 (de) | Triazolyl-cumarine | |
| DE3029746A1 (de) | Organische verbindungen, deren herstellung und verwendung | |
| DE2158304A1 (de) | Delta 2-Pyrazolinderivate, ihre Herstellung und Verwendung als optische Aufheller | |
| DE1939620C (de) | Naphthalimiddenvate und ihre Verwendung | |
| DE899042C (de) | Verfahren zur Herstellung von neuen 4, 4'-Diaminostilbendisulfon- oder -dicarbonsaeuren | |
| AT204547B (de) | Verfahren zur Herstellung von neuen Oxyketonen | |
| DE2604699A1 (de) | Neue basische azofarbstoffe und deren additionssalze mit saeuren | |
| DE2507459C3 (de) | 4,5-Dialkoxy-N-cycloammoniumnaphthalimide |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) | ||
| 8327 | Change in the person/name/address of the patent owner |
Owner name: PCUK-PRODUITS CHIMIQUES UGINE KUHLMANN, 92400 COUR |
|
| 8328 | Change in the person/name/address of the agent |
Free format text: BERG, W., DIPL.-CHEM. DR.RER.NAT. STAPF, O., DIPL.-ING. SCHWABE, H., DIPL.-ING. SANDMAIR, K., DIPL.-CHEM. DR.JUR. DR.RER.NAT., PAT.-ANW., 8000 MUENCHEN |
|
| 8327 | Change in the person/name/address of the patent owner |
Owner name: I.C.I. FRANCOLOR S.A., CLAMART, FR |
|
| 8328 | Change in the person/name/address of the agent |
Free format text: SCHWABE, H., DIPL.-ING. SANDMAIR, K., DIPL.-CHEM. DR.JUR. DR.RER.NAT. MARX, L., DIPL.-PHYS. DR.RER.NAT., PAT.-ANW., 8000 MUENCHEN |