Patent US4643770A successfully refreshed from Google Patents.
US4643770A
Expired / Lapsed
US
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Amine-free, easily dispersible diarylide yellow pigment compositions
Assignee: BASF Corp
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Filing: 1985-04-12
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Granted: 1987-02-17
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Expires: 2005-04-12
Abstract
Abstract Diarylide yellow pigment compositions comprising the reaction product of tetrazotized 3,3'-dichlorobenzidine coupled into an acetoacetarylide, and, a ketimine formed by the reaction of a primary amine and an acetoacetarylide. The ketimine-containing diarylide yellow pigment compositions have improved color strength, improved transparency and contain essentially no free primary amine. Printing inks manufactured with the diarylide yellow pigment compositions of this invention have increased color strength, increased transparency, decreased degradation of publication gravure ink vehicles and decreased acidic fountain solution emulsification in offset ink printing processes.
Inventors
- 👤 Byron G. Hays
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-26 17:27
CPC Classifications
C; C09; C09D; C09D11/00; C09D11/02; C09D11/03; C09D11/037; C09B; C09B67/00; C09B67/0033; C09B67/0046; C09B67/0055
Claims Analysis
Total Claims: 12
Claim 1
Independent Claim
151 words
A diarylide yellow pigment composition manufactured by the method comprising forming a ketimine by reacting a pimary amine with an acetoacetarylide, reacting through a coupling reaction an acetoacetarylide with an excess of a tetrazonium salt of 3,3'-dichlorobenzidine, and subsequently further coupling the excess tetrazonium salt with the ketimine; or reacting through a coupling reaction an excess of a tetrazonium salt of 3,3'-dichlorobenzidine, and the ketimine, and subsequently further coupling the excess tetrazonium salt with an acetoacetarylide; or reacting through a coupling reaction a tetrazonium salt of 3,3'-dichlorobenzidine, an acetoacetarylide, and the ketimine, substantially simultaneously; resulting in a diarylide yellow pigment composition comprising (a) the tetrazonium salt of 3,3'-dichlorobenzidine coupled with the acetoacetarylide; and (b) the tetrazonium salt of 3,3'-dichlorobenzidine coupled with the ketimine; and, (c) the tetrazonium salt of 3,3'-dichlorobenzidine coupled with the ketimine and the acetoacetarylide, said composition having easy dispersibility, improved color strength and essentially no free primary amine.
Claim 2
Dependent Claim
151 words
A diarylide yellow pigment composition manufactured by the method comprising forming a ketimine by reacting a pimary amine with an acetoacetarylide, reacting through a coupling reaction an acetoacetarylide with an excess of a tetrazonium salt of 3,3'-dichlorobenzidine, and subsequently further coupling the excess tetrazonium salt with the ketimine; or reacting through a coupling reaction an excess of a tetrazonium salt of 3,3'-dichlorobenzidine, and the ketimine, and subsequently further coupling the excess tetrazonium salt with an acetoacetarylide; or reacting through a coupling reaction a tetrazonium salt of 3,3'-dichlorobenzidine, an acetoacetarylide, and the ketimine, substantially simultaneously; resulting in a diarylide yellow pigment composition comprising (a) the tetrazonium salt of 3,3'-dichlorobenzidine coupled with the acetoacetarylide; and (b) the tetrazonium salt of 3,3'-dichlorobenzidine coupled with the ketimine; and, (c) the tetrazonium salt of 3,3'-dichlorobenzidine coupled with the ketimine and the acetoacetarylide, said composition having easy dispersibility, improved color strength and essentially no free primary amine.
Claim 3
Dependent Claim
24 words
The diarylide yellow pigment composition of claim 1 wherein the acetoacetarylide is selected from the group consisting of acetoacetanilide, acetoacet-2,4,-xylidide, acetoacet-o-anisidide, acetoacet-o-toluidide, and acetoacet-2,5-dimethoxy-4-chloranilide.
Claim 4
Dependent Claim
18 words
The diarylide yellow pigment composition of claim 1 wherein the acetoacetarylide reacted with the primary amine is acetoacetanilide.
Claim 5
Dependent Claim
26 words
The diarylide yellow pigment composition of claim 3 wherein the primary amine is selected from the group consisting of aliphatic amines, cycloaliphatic amines and polycyclic amines.
Claim 6
Dependent Claim
27 words
The diarylide yellow pigment composition of claim 4, wherein the primary amine is selected from the group consisting of C 18-22 tertiary alkyl amine, 1-adamantylamine and dehydroabietylamine.
Claim 7
Independent Claim
154 words
A method of manufacturing a diarylide yellow pigment composition comprising initially forming a ketimine by reacting a primary amine with an acetoacetarylide, then reacting through a coupling reaction an acetotacetarylide with an excess of a tetrazonium salt of 3,3'-dichlorobenzidine, and subsequently further coupling the excess tetrazonium salt with the ketimine; or reacting through a coupling reaction and excess of a tetrazomium salt of 3,3'-dichlorobenzidine, and the ketimine, and subsequently further coupling the excess tetrazonium salt with an acetoacetarylide; or reacting through a coupling reaction a tetrazonium salt of 3,3'-dichlorobenzidine, an acetoacetarylide, and the ketimine, substantially simultaneously thereby resulting in a diarylide yellow pigment composition comprising: (a) the tetrazonium salt of 3,3'-dichlorobenzidine, coupled with the acetoacetarylide; and (b) the tetrazonium salt of 3,3'-dichlorobenzidine coupled with the ketimine; and, (c) the tetrazonium salt of 3,3'-dichlorobenzidine coupled with the ketimine and the acetoacetarylide, said composition having easy dispersibility, improved color strength and essentially no free primary amine.
Claim 8
Independent Claim
154 words
A method of manufacturing a diarylide yellow pigment composition comprising initially forming a ketimine by reacting a primary amine with an acetoacetarylide, then reacting through a coupling reaction an acetotacetarylide with an excess of a tetrazonium salt of 3,3'-dichlorobenzidine, and subsequently further coupling the excess tetrazonium salt with the ketimine; or reacting through a coupling reaction and excess of a tetrazomium salt of 3,3'-dichlorobenzidine, and the ketimine, and subsequently further coupling the excess tetrazonium salt with an acetoacetarylide; or reacting through a coupling reaction a tetrazonium salt of 3,3'-dichlorobenzidine, an acetoacetarylide, and the ketimine, substantially simultaneously thereby resulting in a diarylide yellow pigment composition comprising: (a) the tetrazonium salt of 3,3'-dichlorobenzidine, coupled with the acetoacetarylide; and (b) the tetrazonium salt of 3,3'-dichlorobenzidine coupled with the ketimine; and, (c) the tetrazonium salt of 3,3'-dichlorobenzidine coupled with the ketimine and the acetoacetarylide, said composition having easy dispersibility, improved color strength and essentially no free primary amine.
Claim 9
Dependent Claim
21 words
The method of claim 6 wherein the acetoacetarylide is selected from the group consisting of acetoacetanilide, acetoacet-2,4-xylidide, acetoacet-o-toluidide, acetoacet-o-anisidide and acetoacet-2,5-dimethoxy-4-chloranilide.
Claim 10
Dependent Claim
23 words
The method of claim 6 wherein the primary amine is selected from the group consisting of aliphatic amines, cycloaliphatic amines and polycyclic amines.
Claim 11
Dependent Claim
26 words
The method of claim 8 wherein the primary amine is selected from the group consisting of C 18-22 tertiary aklyl amines, 1-adamantyl amine and dehydroabietly amine.
Claim 12
Dependent Claim
33 words
A printing ink consisting essentially of a vehicle and a diarylide yellow pigment composition wherein the improvement comprises a diarylide yellow pigment comprising the pigment of claims 1, 2, 3, 4 or 5.
References Cited (Backward Citations)
US3991044A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1990-02-16 | 1990-08-18 | 1991-02-17 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1994-02-16 | 1994-08-18 | 1995-02-17 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1998-02-16 | 1998-08-18 | 1999-02-17 | $7700.00 | Window Closed / Lapsed |