DE2842469A1 - Bis-n-dialkylcarbamoyl-chinacridone, verfahren zu ihrer herstellung und ihre verwendung - Google Patents
Bis-n-dialkylcarbamoyl-chinacridone, verfahren zu ihrer herstellung und ihre verwendungInfo
- Publication number
- DE2842469A1 DE2842469A1 DE19782842469 DE2842469A DE2842469A1 DE 2842469 A1 DE2842469 A1 DE 2842469A1 DE 19782842469 DE19782842469 DE 19782842469 DE 2842469 A DE2842469 A DE 2842469A DE 2842469 A1 DE2842469 A1 DE 2842469A1
- Authority
- DE
- Germany
- Prior art keywords
- parts
- bis
- compounds
- pigment
- 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.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims description 4
- 238000004519 manufacturing process Methods 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 12
- 239000000049 pigment Substances 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 239000003973 paint Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 239000004033 plastic Substances 0.000 claims description 3
- 229920003023 plastic Polymers 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 230000000485 pigmenting effect Effects 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 8
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- 230000007935 neutral effect Effects 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000001054 red pigment Substances 0.000 description 5
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- 229920000137 polyphosphoric acid Polymers 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000000740 bleeding effect Effects 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 238000006798 ring closing metathesis reaction Methods 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- FVLUGNOOEZYDNV-UHFFFAOYSA-N 2,5-bis(4-methylanilino)terephthalic acid Chemical compound C1=CC(C)=CC=C1NC(C(=C1)C(O)=O)=CC(C(O)=O)=C1NC1=CC=C(C)C=C1 FVLUGNOOEZYDNV-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 125000005118 N-alkylcarbamoyl group Chemical group 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
- 125000005521 carbonamide group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000000203 mixture Chemical group 0.000 description 1
- YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- C09B48/00—Quinacridones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782842469 DE2842469A1 (de) | 1978-09-29 | 1978-09-29 | Bis-n-dialkylcarbamoyl-chinacridone, verfahren zu ihrer herstellung und ihre verwendung |
| EP79103527A EP0011105B1 (de) | 1978-09-29 | 1979-09-19 | Bis-N-dialkylcarbamoyl-chinacridone, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE7979103527T DE2962151D1 (en) | 1978-09-29 | 1979-09-19 | Bis-n-dialkylcarbamyl-quinacridones, process for their preparation and their application |
| JP12429379A JPS5548249A (en) | 1978-09-29 | 1979-09-28 | Bissnndialkylcarbamoyllquinacridone*its manufacture and pigment made thereof |
| BR7906237A BR7906237A (pt) | 1978-09-29 | 1979-09-28 | Compostos processo para a sua producao e sua aplicacao |
| MX179458A MX152117A (es) | 1978-09-29 | 1979-09-28 | Procedimiento para la preparacion de pigmentos de bis-n-dialquilcarbanoil-quinacridona |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782842469 DE2842469A1 (de) | 1978-09-29 | 1978-09-29 | Bis-n-dialkylcarbamoyl-chinacridone, verfahren zu ihrer herstellung und ihre verwendung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2842469A1 true DE2842469A1 (de) | 1980-04-10 |
Family
ID=6050854
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19782842469 Withdrawn DE2842469A1 (de) | 1978-09-29 | 1978-09-29 | Bis-n-dialkylcarbamoyl-chinacridone, verfahren zu ihrer herstellung und ihre verwendung |
| DE7979103527T Expired DE2962151D1 (en) | 1978-09-29 | 1979-09-19 | Bis-n-dialkylcarbamyl-quinacridones, process for their preparation and their application |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE7979103527T Expired DE2962151D1 (en) | 1978-09-29 | 1979-09-19 | Bis-n-dialkylcarbamyl-quinacridones, process for their preparation and their application |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0011105B1 (enExample) |
| JP (1) | JPS5548249A (enExample) |
| BR (1) | BR7906237A (enExample) |
| DE (2) | DE2842469A1 (enExample) |
| MX (1) | MX152117A (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4560580A (en) * | 1982-09-30 | 1985-12-24 | Phillips Petroleum Company | Process for encapsulating articles with optional laser printing |
| US4443571A (en) * | 1982-09-30 | 1984-04-17 | Phillips Petroleum Company | Laser printable polyarylene sulfide compositions |
| JPS6412232A (en) * | 1987-07-03 | 1989-01-17 | Yamato Scale Co Ltd | Number combination scale |
| JP2751078B2 (ja) * | 1989-12-12 | 1998-05-18 | 原子燃料工業株式会社 | 原子炉燃料集合体用スペーサー及び燃料集合体 |
| JP2003096324A (ja) * | 2001-09-27 | 2003-04-03 | Dainippon Ink & Chem Inc | キナクリドンスルホン酸誘導体の製造方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1960896C3 (de) * | 1969-12-04 | 1978-11-30 | Hoechst Ag, 6000 Frankfurt | Lineare trans-Chinacridon-Pigmente, Verfahren zu ihrer Herstellung und mit ihnen gefärbte Lacke, Druckfarben und Kunststoffe |
| DE1960897C3 (de) * | 1969-12-04 | 1978-11-30 | Hoechst Ag, 6000 Frankfurt | Lineare trans- Chinacridon-Pigmente, Verfahren zu ihrer Herstellung und mit ihnen gefärbte Lacke, Druckfarben und Kunststoffe |
| DE2148866C3 (de) * | 1971-09-30 | 1974-05-30 | Farbwerke Hoechst Ag, Vormals Meister Lucius & Bruening, 6000 Frankfurt | Chinacridonpigmentgemische und Verfahren zu ihrer Herstellung |
-
1978
- 1978-09-29 DE DE19782842469 patent/DE2842469A1/de not_active Withdrawn
-
1979
- 1979-09-19 EP EP79103527A patent/EP0011105B1/de not_active Expired
- 1979-09-19 DE DE7979103527T patent/DE2962151D1/de not_active Expired
- 1979-09-28 JP JP12429379A patent/JPS5548249A/ja active Granted
- 1979-09-28 MX MX179458A patent/MX152117A/es unknown
- 1979-09-28 BR BR7906237A patent/BR7906237A/pt not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6241267B2 (enExample) | 1987-09-02 |
| DE2962151D1 (en) | 1982-03-25 |
| MX152117A (es) | 1985-05-30 |
| EP0011105A1 (de) | 1980-05-28 |
| BR7906237A (pt) | 1980-05-27 |
| JPS5548249A (en) | 1980-04-05 |
| EP0011105B1 (de) | 1982-02-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8130 | Withdrawal |