ES344876A1 - Procedure for the preparation of disazoic pigments. (Machine-translation by Google Translate, not legally binding) - Google Patents
Procedure for the preparation of disazoic pigments. (Machine-translation by Google Translate, not legally binding)Info
- Publication number
- ES344876A1 ES344876A1 ES344876A ES344876A ES344876A1 ES 344876 A1 ES344876 A1 ES 344876A1 ES 344876 A ES344876 A ES 344876A ES 344876 A ES344876 A ES 344876A ES 344876 A1 ES344876 A1 ES 344876A1
- Authority
- ES
- Spain
- Prior art keywords
- pigments
- disazoic
- translation
- procedure
- preparation
- 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
- 239000000049 pigment Substances 0.000 title abstract 4
- 238000000034 method Methods 0.000 title 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 230000008878 coupling Effects 0.000 abstract 2
- 238000010168 coupling process Methods 0.000 abstract 2
- 238000005859 coupling reaction Methods 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 239000003960 organic solvent Substances 0.000 abstract 2
- 239000000243 solution Substances 0.000 abstract 2
- BFCFYVKQTRLZHA-UHFFFAOYSA-N 1-chloro-2-nitrobenzene Chemical class [O-][N+](=O)C1=CC=CC=C1Cl BFCFYVKQTRLZHA-UHFFFAOYSA-N 0.000 abstract 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 238000013019 agitation Methods 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 239000012670 alkaline solution Substances 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- IFVTZJHWGZSXFD-UHFFFAOYSA-N biphenylene Chemical group C1=CC=C2C3=CC=CC=C3C2=C1 IFVTZJHWGZSXFD-UHFFFAOYSA-N 0.000 abstract 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 abstract 1
- 150000001989 diazonium salts Chemical class 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 229910052739 hydrogen Chemical group 0.000 abstract 1
- 239000001257 hydrogen Chemical group 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 239000000725 suspension Substances 0.000 abstract 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
- C09B33/00—Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
- C09B33/02—Disazo dyes
- C09B33/147—Disazo dyes in which the coupling component is a bis -(-o-hydroxy-carboxylic- acid amide)
-
- 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
- C09B41/00—Special methods of performing the coupling reaction
- C09B41/006—Special methods of performing the coupling reaction characterised by process features
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
Disazo pigments are prepared by mixing an acid solution of a diazonium compound with an aqueous alkaline solution of a bis-[2-hydroxynaphthoyl-(3)]-arylenediamine in continuous manner with vigorous agitation, the resulting pigment suspension being continuously withdrawn. In particular coupling components of formula in which R is phenylene or diphenylene and which may be substituted by one or more halogen atoms, alkyl or alkoxy groups and X is halogen or hydrogen or an alkoxy group are used. Preferably, the liquids are mixed in a mixing nozzle and the coupling component may be dissolved with the aid of a solution promoter which may be a water-miscible organic solvent, e.g. alcohols, ethers, bases. The pigments produced are advantageously purified by treating with an organic solvent, e.g. chloronitrobenzenes, pyridine, picoline and quinoline.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1309066A CH477517A (en) | 1966-09-09 | 1966-09-09 | Process for the production of disazo pigments |
| CH1114867 | 1967-08-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES344876A1 true ES344876A1 (en) | 1969-01-01 |
Family
ID=25707866
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES344876A Expired ES344876A1 (en) | 1966-09-09 | 1967-09-08 | Procedure for the preparation of disazoic pigments. (Machine-translation by Google Translate, not legally binding) |
Country Status (7)
| Country | Link |
|---|---|
| BE (1) | BE703662A (en) |
| CH (1) | CH477517A (en) |
| DE (1) | DE1644117A1 (en) |
| ES (1) | ES344876A1 (en) |
| GB (1) | GB1143727A (en) |
| NL (1) | NL6712378A (en) |
| SE (1) | SE314150B (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH477521A (en) * | 1966-08-15 | 1969-08-31 | Ciba Geigy | Process for the production of new disazo dye pigments |
| DE2302482C3 (en) * | 1973-01-19 | 1984-01-05 | Hoechst Ag, 6230 Frankfurt | Disazo pigment, process for its preparation and its use |
| DE2521249C2 (en) * | 1975-05-13 | 1983-11-10 | Bayer Ag, 5090 Leverkusen | Process for the production of opaque organic pigments |
| DE2844634A1 (en) * | 1978-10-13 | 1980-04-24 | Hoechst Ag | METHOD FOR THE CONTINUOUS PRODUCTION OF AZOPIGMENTS |
| EP0095442A1 (en) * | 1982-05-18 | 1983-11-30 | Ciba-Geigy Ag | Disazo pigments, method for their preparation and their use |
| IN169307B (en) * | 1986-05-03 | 1991-09-28 | Hoechst Ag | |
| DE10032019A1 (en) * | 2000-07-01 | 2002-01-10 | Clariant Gmbh | Process for the preparation of disazo condensation pigments in microreactors |
| KR20100016422A (en) * | 2007-04-13 | 2010-02-12 | 바스프 에스이 | Production of finely divided pigments |
-
0
- GB GB1143727D patent/GB1143727A/en not_active Expired
-
1966
- 1966-09-09 CH CH1309066A patent/CH477517A/en not_active IP Right Cessation
-
1967
- 1967-08-30 DE DE19671644117 patent/DE1644117A1/en active Pending
- 1967-09-08 NL NL6712378A patent/NL6712378A/xx unknown
- 1967-09-08 BE BE703662D patent/BE703662A/xx unknown
- 1967-09-08 ES ES344876A patent/ES344876A1/en not_active Expired
- 1967-09-08 SE SE1242667A patent/SE314150B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL6712378A (en) | 1968-03-11 |
| GB1143727A (en) | 1900-01-01 |
| CH477517A (en) | 1969-08-31 |
| BE703662A (en) | 1968-03-08 |
| DE1644117A1 (en) | 1970-10-29 |
| SE314150B (en) | 1969-09-01 |
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