GB2032943A - Diazo Pigments - Google Patents
Diazo Pigments Download PDFInfo
- Publication number
- GB2032943A GB2032943A GB7932858A GB7932858A GB2032943A GB 2032943 A GB2032943 A GB 2032943A GB 7932858 A GB7932858 A GB 7932858A GB 7932858 A GB7932858 A GB 7932858A GB 2032943 A GB2032943 A GB 2032943A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diazo
- amino
- dye
- pigment
- coupling
- 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.)
- Granted
Links
- 239000000049 pigment Substances 0.000 title claims abstract description 27
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 title claims abstract description 23
- 238000000034 method Methods 0.000 claims abstract description 8
- 238000005859 coupling reaction Methods 0.000 claims description 17
- 230000008878 coupling Effects 0.000 claims description 15
- 238000010168 coupling process Methods 0.000 claims description 15
- 150000001412 amines Chemical class 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- QVEXXKXDPXEDMT-UHFFFAOYSA-N NC1CC2C(NC(NC2=C(C1)N)=O)=O Chemical compound NC1CC2C(NC(NC2=C(C1)N)=O)=O QVEXXKXDPXEDMT-UHFFFAOYSA-N 0.000 claims description 5
- WDJHALXBUFZDSR-UHFFFAOYSA-M acetoacetate Chemical compound CC(=O)CC([O-])=O WDJHALXBUFZDSR-UHFFFAOYSA-M 0.000 claims description 3
- GPNNOCMCNFXRAO-UHFFFAOYSA-N 2-aminoterephthalic acid Chemical compound NC1=CC(C(O)=O)=CC=C1C(O)=O GPNNOCMCNFXRAO-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 150000001448 anilines Chemical group 0.000 claims description 2
- 150000004982 aromatic amines Chemical group 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 238000004040 coloring Methods 0.000 claims description 2
- 239000000976 ink Substances 0.000 claims description 2
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 239000003973 paint Substances 0.000 claims description 2
- 239000004033 plastic Substances 0.000 claims description 2
- 229920003023 plastic Polymers 0.000 claims description 2
- ZUVPLKVDZNDZCM-UHFFFAOYSA-N 3-chloro-2-methylaniline Chemical compound CC1=C(N)C=CC=C1Cl ZUVPLKVDZNDZCM-UHFFFAOYSA-N 0.000 claims 2
- 239000000463 material Substances 0.000 claims 2
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 claims 2
- GUMCAKKKNKYFEB-UHFFFAOYSA-N 2,4,5-trichloroaniline Chemical compound NC1=CC(Cl)=C(Cl)C=C1Cl GUMCAKKKNKYFEB-UHFFFAOYSA-N 0.000 claims 1
- GEQNZVKIDIPGCO-UHFFFAOYSA-N 2,4-dimethoxyaniline Chemical compound COC1=CC=C(N)C(OC)=C1 GEQNZVKIDIPGCO-UHFFFAOYSA-N 0.000 claims 1
- AVYGCQXNNJPXSS-UHFFFAOYSA-N 2,5-dichloroaniline Chemical compound NC1=CC(Cl)=CC=C1Cl AVYGCQXNNJPXSS-UHFFFAOYSA-N 0.000 claims 1
- NAZDVUBIEPVUKE-UHFFFAOYSA-N 2,5-dimethoxyaniline Chemical compound COC1=CC=C(OC)C(N)=C1 NAZDVUBIEPVUKE-UHFFFAOYSA-N 0.000 claims 1
- GVBHRNIWBGTNQA-UHFFFAOYSA-N 2-methoxy-4-nitroaniline Chemical compound COC1=CC([N+]([O-])=O)=CC=C1N GVBHRNIWBGTNQA-UHFFFAOYSA-N 0.000 claims 1
- XTTIQGSLJBWVIV-UHFFFAOYSA-N 2-methyl-4-nitroaniline Chemical compound CC1=CC([N+]([O-])=O)=CC=C1N XTTIQGSLJBWVIV-UHFFFAOYSA-N 0.000 claims 1
- DLURHXYXQYMPLT-UHFFFAOYSA-N 2-nitro-p-toluidine Chemical compound CC1=CC=C(N)C([N+]([O-])=O)=C1 DLURHXYXQYMPLT-UHFFFAOYSA-N 0.000 claims 1
- XQVCBOLNTSUFGD-UHFFFAOYSA-N 3-chloro-4-methoxyaniline Chemical compound COC1=CC=C(N)C=C1Cl XQVCBOLNTSUFGD-UHFFFAOYSA-N 0.000 claims 1
- CXNVOWPRHWWCQR-UHFFFAOYSA-N 4-Chloro-ortho-toluidine Chemical compound CC1=CC(Cl)=CC=C1N CXNVOWPRHWWCQR-UHFFFAOYSA-N 0.000 claims 1
- WRZOMWDJOLIVQP-UHFFFAOYSA-N 5-Chloro-ortho-toluidine Chemical compound CC1=CC=C(Cl)C=C1N WRZOMWDJOLIVQP-UHFFFAOYSA-N 0.000 claims 1
- WBSMIPLNPSCJFS-UHFFFAOYSA-N 5-chloro-2-methoxyaniline Chemical compound COC1=CC=C(Cl)C=C1N WBSMIPLNPSCJFS-UHFFFAOYSA-N 0.000 claims 1
- DSBIJCMXAIKKKI-UHFFFAOYSA-N 5-nitro-o-toluidine Chemical compound CC1=CC=C([N+]([O-])=O)C=C1N DSBIJCMXAIKKKI-UHFFFAOYSA-N 0.000 claims 1
- 229940102398 methyl anthranilate Drugs 0.000 claims 1
- 239000000975 dye Substances 0.000 abstract description 9
- 230000007613 environmental effect Effects 0.000 abstract description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 7
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 4
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000000080 wetting agent Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 3
- KQCMTOWTPBNWDB-UHFFFAOYSA-N 2,4-dichloroaniline Chemical compound NC1=CC=C(Cl)C=C1Cl KQCMTOWTPBNWDB-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- URYBQXRJUBJCRK-UHFFFAOYSA-N N-[2,4-dioxo-8-(3-oxobutanoylamino)-4a,5,6,7-tetrahydro-1H-quinazolin-6-yl]-3-oxobutanamide Chemical compound C(CC(=O)C)(=O)NC1CC2C(NC(NC2=C(C1)NC(CC(=O)C)=O)=O)=O URYBQXRJUBJCRK-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- 239000012954 diazonium Substances 0.000 description 2
- 150000001989 diazonium salts Chemical class 0.000 description 2
- WASQWSOJHCZDFK-UHFFFAOYSA-N diketene Chemical compound C=C1CC(=O)O1 WASQWSOJHCZDFK-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 235000010288 sodium nitrite Nutrition 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- SVDAJTZKOJZQFC-UHFFFAOYSA-N 2,4-dichlorobenzenediazonium Chemical compound ClC1=CC=C([N+]#N)C(Cl)=C1 SVDAJTZKOJZQFC-UHFFFAOYSA-N 0.000 description 1
- JCYPECIVGRXBMO-UHFFFAOYSA-N 4-(dimethylamino)azobenzene Chemical compound C1=CC(N(C)C)=CC=C1N=NC1=CC=CC=C1 JCYPECIVGRXBMO-UHFFFAOYSA-N 0.000 description 1
- 101000623895 Bos taurus Mucin-15 Proteins 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- KUDPGZONDFORKU-UHFFFAOYSA-N n-chloroaniline Chemical compound ClNC1=CC=CC=C1 KUDPGZONDFORKU-UHFFFAOYSA-N 0.000 description 1
- VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical compound [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 description 1
- VLZLOWPYUQHHCG-UHFFFAOYSA-N nitromethylbenzene Chemical compound [O-][N+](=O)CC1=CC=CC=C1 VLZLOWPYUQHHCG-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 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
- C09B33/153—Disazo dyes in which the coupling component is a bis-(aceto-acetyl amide) or a bis-(benzoyl-acetylamide)
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
A diazo pigment dye having the formula <IMAGE> wherein D is the residue of an aromatic diazo component without water-solubilizing groups. The dyes possess good tinctorial and advantageous environmental properties. Methods for preparing the dyes are disclosed.
Description
SPECIFICATION
Disazo Pigments
Background of the Invention 1. Field of the Invention
This invention relates to diazo pigments and particularly to diazo pigments derived from novel coupling agents.
2. Description of the Prior Art
Diazo coloring agents, as a class, are well known and desirable because of their brilliant shades and good tinctorial properties. The diazo moieties of these pigments are usually prepared with coupling agents. However, one of the problems observed with such pigments is that they often require the presence of solubilizing agents which represent environmental pollutants.
Summary of the Invention
We have discovered new diazo pigments which provide both excellent properties as pigments and also avoid the environmental problems resulting from the use of certain stabilizers.
More particularly, the diazo pigment dyes of the present invention have the formula
in which D represents the residue of an aromatic diazo component without water-solubilizing groups.
Pigment dyes of formula I are obtained by coupling diazotized amines which contain the D residue, with 6,8-diacetoacelainino-2,4-dioxotetrahydrnquinazoline (formula II).
The new diazo pigment dyes do not only represent an interesting enrichment to the range of pigment dyes available, but they also are distinguished by an environment-compatible method of manufacture because, as a result of the relatively good alkali solubility of the coupling components, the use of effluent contaminating solubilizers is omitted. On the basis of these advantageous properties, these diazo pigment dyes may be used in all areas of application of the pigment industry. They are, for example, well suited for the coloring of plastics, especially of PVC, as well as for the preparation of paints and printing inks.
Coupling component II is prepared by reacting 6,8-diamino-2,4-dioxotetrahydroquinazoline (Beilstein 25 1 699) with diketene.
Description of the Preferred Embodiment
The coupling normally is carried out in such a manner that an acidic solution of the diazonium salt is added dropwise to an acetic acid suspension of the coupling component with a pH of ca. 5, with a final pH of ca. 4 being obtained. This step may optionally be carried out in the presence of a wetting agent.
The suspension of the coupling component is obtained by adding the coupling component, dissolved in alkali, dropwise into aqueous acetic acid at OOC. If a wetting agent is added, it is preferably added to the alkaline solution of 6,8-diacetoacetylamino-2,4-dioxotetrahydroquinazoline.
In another feasible coupling reaction, the coupling component dissolved in alkali, is added dropwise to a solution of diazonium salt, which has been buffered to a pH of 3 to 4. A final pH of 6 to 7 is obtained.
As wetting agents, cationic substances, such as, for example, fatty amines and their salts, nonionic products, such as, for example, sorbitan esters of fatty acids, or anionic wetting agents, such as, for example, aryl-alkyl sulfonates, may be used. Polyoxyethylated fatty amines may also be employed with success.
As diazo components, aromatic amines without water-solubilizing groups, which are conventionally used for the manufacture of pigments are employed. Examples of such amines are the anilines, substituted with chloro, nitro, alkyl or alkoxy groups or by carbonamido groups.
The pigments of formula (I) do not always exist in the physical form which is optimum for their intended application. They may, however, be converted into the desired form by known methods, such as, for example, salt grinding or heating in a solvent.
Obviously, for the preparation of the diazo pigment dye of formula (I), it is also possible to use an acetoacetate pigment which is obtained by coupling an acetoacetate with a diazotized amine, which contains the D residue, and condensing with 6,8-diamino-2,4-dioxotetrahydroquinazoline in a solvent.
The following examples illustrate the present invention:
Example 1
Preparation of the Coupling Component:
6,8-diamino-2,4-dioxotetrahydroquinazoline (115.32 g), dissolved with heating in Nmethylpyrrolidone, is mixed with 151.34 g of diketene. In order to complete the reaction, stirring is continued at a higher temperature. The clarified and cooled reaction solution is added to 6,000 g of water with stirring in order to precipitate the product. The suspension is filtered with suction, washed and dried.
Example 2
Coupling of diazotized 2,4-dichloroaniline with 6,8-diacetoacetyla mino-2,4- dioxotetrahydroquinazoline:
2,4-dichloroaniline (32.4 g, 0.2 moles) is converted into a paste with 500 g of water and 82.95 g of concentrated hydrochloric acid, heated, cooled to OOC and diazotized with 14.0 g of dissolved sodium nitrite, stirred for an additional time and filtered with suction. 6,8-diacetoacetylamino-2,4- dioxotetrahydroquinazoline (36.8 g, 0.102 moles) are dissolved in 750 g of water with 31.2 g of sodium hydroxide solution. The coupling component is reprecipitated by being added dropwise to a mixture of 250 g of water/ice and 101.21 g of 60% acetic acid. To this suspension, the diazo solution is added dropwise.Stirring is continued for some time in order to complete the coupling reaction. The pigment suspension is filtered with suction and washed until it is neutral. The filter cake is dried and the crude product obtained is subjected to a solvent finishing in dimethyl sulfoxide.
Example 3
The procedure is identical with that in Example 2 with the exception, however, that, instead of 2,4-dichloroaniline, the following diazo components are used in equimojar amounts:
Diazo Component: Shade:
0.20 moles, 32. 4 g of 2,5-dichloro- yellow with greenish tint
aniline
0.20 moles, 39.2 g of 2,4,5-tri- yellow
chloroaniline
0.20 moles, 28.3 g of 2-amino-4- yellow with greenish tint
chlorotoluene
0.20 moles, 28.3 g of 2-amino-5- yellow with reddish tint
chlorotoluene
0.20 moles, 28.3 g of 2-amino-6- yellow with greenish tint
chlorotoluene
0.20 moles, 30.42 g of 2-amino-4- yellow with greenish tint
nitroluene
0.20 moles, 30.8 g of 2-amino-5- yellow with reddish tint
nitrotoluene
0.20 moles, 30.44 g of 3-nitro-4- yellow with reddish tint
aminotoluene
0.20 moles, 33.64 g of 2-methoxy-4- reddish yellow
nitroaniline
Diazo Component: Shade: 0.20 moles, 48.46 g of 3-amino4- yellow with greenish tint
methoxy benzanalide 0.20 moles, 31.52 g of 4-chloro-2- yellow
aminoanisole
0.20 moles, 31.7 g of 2-chloro-4- yellow with reddish tint
aminoanisole
0.20 moles, 30.64 g of 2,4-dimethoxy- yellow with reddish tint
aniline
0.20 moles, 30.64 g of 2,5-dimethoxy- yellow with reddish tint
aniline
0.20 moles, 30.24 g of methyl yellow with greenish tint
anthranilate
0.20 moles, 41.84 g of dimethyl ester yellow with greenish tint.
of 2-aminoterephthalic acid
Example 4
Process for the Preparation of a Pigment in Accordance with the Present Invention by
Condensation in a Solvent: 2A-dichloroaniline (32.4 g) is stirred for 3 hours in 89.83 g of 30.59G hydrochloric acid, diluted
with ice water and diazotized by the addition of 14.1 g of sodium nitrite, dissolved in water.
Ethyl acetoacetate (26.67 g) is dissolved in 181.54 g of 80% acetic acid and mixed with a
solution of 27.2 g of sodium hydroxide in water, the temperature increasing to 300C. The diazo solution is rapidly added dropwise to the solution of the coupling component. After continuing to stir for a further 2 hours, the pigment suspension is filtered off with suction, washed until neutral and dried.
The pale yellow ester pigment obtained (6.67 g) is suspended together with 1.92 g of 6,8
diamino-2,4-dioxotetrahydroquinazoline in nitrobenzene and heated under reflux. The ethyl alcohol,
formed by the condensation, is distilled off. After 3 hours, the reaction product is filtered off, washed
with benzene and petroleum ether and dried.
Claims (6)
1. A diazo pigment dye having the formula
wherein D is the residue of an aromatic diazo component without a water-solubilizing group.
2. The dye of claim 1 wherein the diazo component is an aromatic amine selected from the group consisting of anilines substituted with chloro, nitro, alkyl, alkoxv or carbonamido.
3. The dye of claim 1 wherein the diazo component is selected from the group consisting of: 2,5-dichloroaniline, 2,4,5-trichloroaniline, 2-amino4-chlorotoluene,
2-amino-5-chlorotoluene,
2-amino-6-chlorotoluene,
2-amino-4-nitrotoluene,
2-amino-5-nitrotoluene,
3-nitro-4-aminotoluene,
2-methoxy-4-nitroaniline,
3-amino-4-methoxy benzanalide, 4-chloro-2-aminoanisole, 2-chloro-4-aminoanisole, 2,4-dimethoxyaniline, 2,5-dimethoxyaniline, methyl anthranilate, and
dimethylester of 2-aminoterephthalic acid.
4. A method for preparing the dye of claim 1 comprising coupling a diazotized amine containing residue D with 6,8-diacetoacetyla m ino-2,4-dioxotetrahydroquinazoline.
5. A method for preparing the dye of claim 1 comprising coupling an acetoacetate with a diazotized amine containing residue D, and condensing this product with 6,8-diamino-2,4dioxotetrahydroquinazoline in a solvent.
6. In a method for coloring materials selected from the group consisting of plastics, paints and printing inks, wherein the material is contacted with a diazo pigment, the improvement which comprises said diazo pigment being the pigment of claim 1.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782841532 DE2841532C2 (en) | 1978-09-23 | 1978-09-23 | New disazo pigment dyes, processes for their production and their use for coloring plastics, lacquers and printing inks |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| GB2032943A true GB2032943A (en) | 1980-05-14 |
| GB2032943B GB2032943B (en) | 1982-10-13 |
Family
ID=6050287
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB7932858A Expired GB2032943B (en) | 1978-09-23 | 1979-09-21 | Disazo pigments |
Country Status (3)
| Country | Link |
|---|---|
| CH (1) | CH644884A5 (en) |
| DE (1) | DE2841532C2 (en) |
| GB (1) | GB2032943B (en) |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH478205A (en) * | 1966-05-23 | 1969-09-15 | Bayer Ag | Process for the preparation of sulfonic acid group-free azo dyes |
| CH515308A (en) * | 1967-12-06 | 1971-11-15 | Bayer Ag | Process for the preparation of bis (N-acylamino-phthalimide) -disazo dyes |
| DE2329781C2 (en) * | 1973-06-12 | 1986-06-05 | Hoechst Ag, 6230 Frankfurt | Benzoxazinedione azo pigments, process for their preparation and their use as colorants |
| CH585247A5 (en) * | 1973-08-24 | 1977-02-28 | Sandoz Ag | Yellow disazo pigments contg. substd. methyl quinoline gps. - for plastics, coatings, textiles, paper etc. |
| CH599299A5 (en) * | 1973-10-30 | 1978-05-31 | Ciba Geigy Ag | |
| CH620702A5 (en) * | 1974-03-25 | 1980-12-15 | Chemetron Corp | Process for conditioning yellow disazo diimide dyestuffs |
-
1978
- 1978-09-23 DE DE19782841532 patent/DE2841532C2/en not_active Expired
-
1979
- 1979-09-20 CH CH850179A patent/CH644884A5/en not_active IP Right Cessation
- 1979-09-21 GB GB7932858A patent/GB2032943B/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB2032943B (en) | 1982-10-13 |
| DE2841532A1 (en) | 1980-03-27 |
| CH644884A5 (en) | 1984-08-31 |
| DE2841532C2 (en) | 1983-01-05 |
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| PCNP | Patent ceased through non-payment of renewal fee |