US2427911A - 3, 5-diketo pyrazolidine color formers - Google Patents
3, 5-diketo pyrazolidine color formers Download PDFInfo
- Publication number
- US2427911A US2427911A US591830A US59183045A US2427911A US 2427911 A US2427911 A US 2427911A US 591830 A US591830 A US 591830A US 59183045 A US59183045 A US 59183045A US 2427911 A US2427911 A US 2427911A
- Authority
- US
- United States
- Prior art keywords
- colour
- image
- diketo
- pyrazolidine
- layer
- 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 - Lifetime
Links
- DNTVKOMHCDKATN-UHFFFAOYSA-N pyrazolidine-3,5-dione Chemical compound O=C1CC(=O)NN1 DNTVKOMHCDKATN-UHFFFAOYSA-N 0.000 title 1
- -1 amino, substituted amino Chemical group 0.000 description 29
- 238000000034 method Methods 0.000 description 18
- 125000001183 hydrocarbyl group Chemical group 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 12
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 12
- 239000000839 emulsion Substances 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 9
- 125000000623 heterocyclic group Chemical group 0.000 description 9
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 8
- 125000003545 alkoxy group Chemical group 0.000 description 7
- 239000000975 dye Substances 0.000 description 7
- 125000005429 oxyalkyl group Chemical group 0.000 description 6
- 239000004332 silver Substances 0.000 description 5
- 229910052709 silver Inorganic materials 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical compound [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 150000008049 diazo compounds Chemical class 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- USPWKWBDZOARPV-UHFFFAOYSA-N pyrazolidine Chemical compound C1CNNC1 USPWKWBDZOARPV-UHFFFAOYSA-N 0.000 description 2
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- KOOMFXGDLMRWSN-UHFFFAOYSA-N n-phenylnitrous amide Chemical compound O=NNC1=CC=CC=C1 KOOMFXGDLMRWSN-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 150000004060 quinone imines Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/32—Colour coupling substances
- G03C7/36—Couplers containing compounds with active methylene groups
- G03C7/38—Couplers containing compounds with active methylene groups in rings
- G03C7/381—Heterocyclic compounds
- G03C7/3815—Heterocyclic compounds with one heterocyclic ring
Definitions
- This invention relates to colour photography and particularly to dyestulf intermediates for use in 'colourphotographic processes.
- the colourcouplers may be present in the developing solution employed, or may be included in a photographic emulsion layer which contains the reduciblesilver salt image, or in an adjacent layer or a layer separated from the said emulsion layer only by a thin water-permeable layer.
- Thedeveloping agent may be, for-example, p-phenylene diamineor its N.N-dialkyl derivatives, e.:g. NN- dimethyl or N .Ndiethyl-p-phen-ylene diamines, or 'homologues thereof, e. g. '5-diethylamino-2- amino-toluene.
- a process of colour photography comprises developing a reducible silver salt image by means of an aromatic primary amino developing agent in the presence of a compound of the general formula:
- R1 and R2 are hydrogen atoms or substituted or unsubstituted hydrocarbon groups, e. g. alkyl, aralkyl or and groups, or heterocyclic groups, e. g. methyl, ethyl or higher alkyl, benzyl, phenyl or naphthyl groups which may be substituted by alkyl, aryl, aralkyl, amino, substituted amino, nitro, hydroXy, alkoxy, oxyalkyl, sulphonic and *carboxylic groups or I halogen atoms.
- hydrocarbon groups e. g. alkyl, aralkyl or and groups, or heterocyclic groups, e. g. methyl, ethyl or higher alkyl, benzyl, phenyl or naphthyl groups which may be substituted by alkyl, aryl, aralkyl, amino, substituted amino, nitro, hydroXy, alkoxy, oxyal
- '1:2'-diphenyl-3.5-diketo pyrazolidine may be prepared from hydrazobenzene, diethyl 'malonate or other dialkyl malonate and-sodium ethoxide in the manner described in Berichte der DeutscheniCheinischen Deutschen, volume 73B, pages 8204322, and other compounds can be prepared analogously by varying the nature of the starting materials.
- p.p-dichloro-hydrazobenzene the corresponding 1.2-di-(p-chlor phenyl) -3.5-diketo-pyrazolidine (melting point 177 'C.) may be obtained.
- the colour-couplersof this invention yield acct: magenta images suitable for use in three-colour subtractive colour processes.
- the colour-"couplers of this invention may b included in a developing solution containing an aromatic primary amino developingagenu-or may be included in a silver halide emulsion layer, or in a water-permeable colloid layer coated next to a silver halide emulsion layer, or separated therefrom only by a thin water-permeable colloid layer.
- the colour-couplers of this invention may be used in any of the colour processes of U. S. Patents Nos. 2,350,380, 2,363,764 and 2,369,171 and British Patents Nos. 551,116, 551,117, 554,302 and 556,858.
- the formation of coloured images by means of the colour-couplers of this invention may be applied to the development of a reducible silver salt image which is an original latent image formed in the emulsion layer by exposure to light or which is an image obtained by the conversion of a silver image to a reducible silver salt image,
- the colour-couplers of the invention may also be employed in other colour photographic processes, e. g. process in which the dye is formed by direct coupling between the colour-coupler and a nitroso aniline, e. g. p-nitroso dialkyl aniline, or between the colour-coupler and a diazo compound.
- a colourcoupler may be present in a layer containing a reducible silver salt image, such image, developed with an aromatic primary amino developing:
- the agent forming an azomethine dye image in situ with the developed silver image, the residual colour-coupler coupled with a diazo compound applied in solution to the photographic element, and the original azomethine dye image bleached out, leaving only the azo dye image in the layer.
- a process of colour photography which comprises developing a reducible silver salt image in a photographic element by means of an aromatic primary amino developing agent in the presence of a compound of the general formula:
- each of R1 and R2 is a group selected from the class consisting of hydrogen atoms, hydrocarbon groups, amino-, nitro-, hydroxy-, alkoxy-, oxyalkyl-, su1fonic-, carboXylic-, and halogensubstituted hydrocarbon groups and heterocyclic groups.
- a process of colour photography which comprises developing a reducible silver salt in a photographic element by means of a solution of an aromatic primary amino developing agent containing a compound of the general formula:
- each of R1 and R2 is a group selected from the class consisting of hydrogen atoms, hydrocarbon groups, amino-, nitro-, hydroxy-, alkoxy-, oxyalkyl-, sulfonic-, carboxylic-, and halogensubstituted hydrocarbon groups and heterocyclic groups.
- a photographic element for colour photography which comprises a support hearing at least one layer of a light-sensitive silver halide emulsion containing a compound of the general formula:
- each of R1 and R2 is a group selected from the class consisting of hydrogen atoms, hydrocarbon groups, amino-, nitro-, hydroxy-, alkoxy-, oxyalkyl-, sulfonic-, carboxylic-, and halogensubstituted hydrocarbon groups and heterocyclic groups,
- a process of colour photography which comprises forming a reducible silver salt image in an emulsion layer of a photographic element which contains a compound of the general formula:
- each of R1 and R2 is a group selected from the class consisting of hydrogen atoms, hydrocarbon groups, amin0-, nitro-, hydroxy-, alkoxy-, oxyalky1-, sulfonic-, carboxylic-, and halogensubstituted hydrocarbon groups and heterocyclic groups, and developing said image with an aromatic primary amino developing agent.
- a process of colour photography which comprises forming a reducible silver salt image in an emulsion layer of a photographic element which contains a compound of the general formula:
- R1N---NR2 to C0 Ci where each of R1 and R2 is a group selected from the class consisting of hydrogen atoms, hydrocarbon groups, amino-, nitro-, hydroxy-, alkoxy-, oxyalkyl-, sulfonic-, carboxylic-, and halogensubstituted hydrocarbon groups and heterocyclic groups, and developing said image with an N,N- dialkyl-p-phenylene diamine.
- a process of colour photography which comprises forming a reducible silver salt image in an emulsion layer of a photographic element which includes, adjacent thereto, a layer containing a compound of the general formula:
- each of R1 and R2 is a group selected from the class consisting of hydrogen atoms, hydrocarbon groups, amino-, nitro-, hydroxy-, alkoxy-, oxya1kyl-, sulfonic-, carboxylic-, and halogensubstituted hydrocarbon groups and heterocyclic groups, and developing said image with an aromatic primary amino developing agent.
- a process of colour photography which comprises forming a reducible silver salt; image in an emulsion layer of a photographic element which includes, adjacent thereto, a layer containing a compound of the general formula:
- each of R1 and R2 is a group selected from the class consisting of hydrogen atoms, hydrocarbon groups, amino-, nitro-, hydroxy-, alkoXy-, oxyalkyl-, sulfonic-, carboxylic-, and halogensubstituted hydrocarbon groups and heterocyclic groups, and developing said image with an N,N- dialkyl-p-phenylene diamine.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Plural Heterocyclic Compounds (AREA)
Description
Patented Sept. 23, 1947 3,5-DIKETOTYRAZOEIDINEGOIJOR LFORMERS John David "Kendall and Douglas James Fry, 'Ilford, "England, assignorsto IlfordLimited, "'Ilford,'England, a British company No Drawing. Application Mayi3, l945ys'ei ial No. 591,830. In Great Britain-May 12,;1944
8 Claims.
1 "This invention relates to colour photography and particularly to dyestulf intermediates for use in 'colourphotographic processes.
Processes of colour phdtography are'wellknown inwhich coloured images are produced'by the development of "reducible silver salt images by means of aromatic primary amino developing agents in "the presence of compounds, generally known as colour-formers or colour-couplers,
which couple with the-oxidation products of such developers, formed during development, to form quinone-imine or azomethine dyes. The colourcouplers may be present in the developing solution employed, or may be included in a photographic emulsion layer which contains the reduciblesilver salt image, or in an adjacent layer or a layer separated from the said emulsion layer only by a thin water-permeable layer. Thedeveloping agent may be, for-example, p-phenylene diamineor its N.N-dialkyl derivatives, e.:g. NN- dimethyl or N .Ndiethyl-p-phen-ylene diamines, or 'homologues thereof, e. g. '5-diethylamino-2- amino-toluene.
Large numbers of colour-couplers have been described in the extensive literature dealing with this type of colour photographic process. The requirements for a satisfactory colour-coupler, however, are rather strict. Thus, it must be capable of ready incorporation into the developing bath or photographic layer into which it is desired to include it, and where it is included .in a photographic layer, neither it nor the dye derived from it must have any substantial tendency to diffuse from such layer, either into adj acent layers of the photographic element, or into processing baths. Moreover, it must be selected so that the colour of the dye obtained from it is suitable for the particular colour process with which it is intended to be used.
According to the present invention a process of colour photography comprises developing a reducible silver salt image by means of an aromatic primary amino developing agent in the presence of a compound of the general formula:
where R1 and R2 are hydrogen atoms or substituted or unsubstituted hydrocarbon groups, e. g. alkyl, aralkyl or and groups, or heterocyclic groups, e. g. methyl, ethyl or higher alkyl, benzyl, phenyl or naphthyl groups which may be substituted by alkyl, aryl, aralkyl, amino, substituted amino, nitro, hydroXy, alkoxy, oxyalkyl, sulphonic and *carboxylic groups or I halogen atoms.
or .quinolyl, .pyridy1,furyl and similar heterocyclic groups.
These compounds may be prepared by anyconvenient'method. Thus, fortexample, '1:2'-diphenyl-3.5-diketo pyrazolidine may be prepared from hydrazobenzene, diethyl 'malonate or other dialkyl malonate and-sodium ethoxide in the manner described in Berichte der DeutscheniCheinischen Gesellschaft, volume 73B, pages 8204322, and other compounds can be prepared analogously by varying the nature of the starting materials. Thus, using p.p-dichloro-hydrazobenzene the corresponding 1.2-di-(p-chlor phenyl) -3.5-diketo-pyrazolidine (melting point 177 'C.) may be obtained. Similarly there may be employed: 4.4' dimeth'oxy hydrazobenzene, '3Z3'-dinitro-hydrazobenzene, dixenyl hydrazine, ditolyl hydrazine, B18-dinaphthyl hydrazine,'2.2'-1epidyl hydrazineand 2.2-quinoly1 hydrazine.
Particular compounds which may be 'used in.
accordancewith the present invention are:
1 -phenyl-3.5-diketo pyrazolidine -1-methyl- 3.5-diketopyrazolidine 1.2-di(4'-Inethoxyphenyl) -3.5-diketo pyrazolidine:
1.2-di(3-nitrophenyl) -3.5-diketo pyrazolidine 1 .2-dixeny1-3 .S-diketo pyrazolidine 1.2-diquinolyl-3.5-diketo pyrazolidine 1.2-ditolyl-3.5-diketo pyrazolidine These compounds are made by t-he' proce's's 'described above using the appropriate reagents.
The colour-couplersof this invention yield acct: magenta images suitable for use in three-colour subtractive colour processes.
The colour-"couplers of this invention may b included in a developing solution containing an aromatic primary amino developingagenu-or may be included in a silver halide emulsion layer, or in a water-permeable colloid layer coated next to a silver halide emulsion layer, or separated therefrom only by a thin water-permeable colloid layer. Thus, for example, the colour-couplers of this invention may be used in any of the colour processes of U. S. Patents Nos. 2,350,380, 2,363,764 and 2,369,171 and British Patents Nos. 551,116, 551,117, 554,302 and 556,858.
The formation of coloured images by means of the colour-couplers of this invention may be applied to the development of a reducible silver salt image which is an original latent image formed in the emulsion layer by exposure to light or which is an image obtained by the conversion of a silver image to a reducible silver salt image,
by the usual bleachingtechnique.
Although this invention is primarily concerned with colour photographic processes in which the dye is formed by the coupling of the colour-couplers of the invention with the oxidation products of an aromatic primary amino developing agent formed in situ during the development of a reducible silver salt image, the colour-couplers of the invention may also be employed in other colour photographic processes, e. g. process in which the dye is formed by direct coupling between the colour-coupler and a nitroso aniline, e. g. p-nitroso dialkyl aniline, or between the colour-coupler and a diazo compound. As an example of this latter type of process a colourcoupler may be present in a layer containing a reducible silver salt image, such image, developed with an aromatic primary amino developing:
agent forming an azomethine dye image in situ with the developed silver image, the residual colour-coupler coupled with a diazo compound applied in solution to the photographic element, and the original azomethine dye image bleached out, leaving only the azo dye image in the layer.
What we claim is:
1. A process of colour photography which comprises developing a reducible silver salt image in a photographic element by means of an aromatic primary amino developing agent in the presence of a compound of the general formula:
CO CO where each of R1 and R2 is a group selected from the class consisting of hydrogen atoms, hydrocarbon groups, amino-, nitro-, hydroxy-, alkoxy-, oxyalkyl-, su1fonic-, carboXylic-, and halogensubstituted hydrocarbon groups and heterocyclic groups.
2. A process of colour photography which comprises developing a reducible silver salt in a photographic element by means of a solution of an aromatic primary amino developing agent containing a compound of the general formula:
where each of R1 and R2 is a group selected from the class consisting of hydrogen atoms, hydrocarbon groups, amino-, nitro-, hydroxy-, alkoxy-, oxyalkyl-, sulfonic-, carboxylic-, and halogensubstituted hydrocarbon groups and heterocyclic groups.
3. A photographic element for colour photography which comprises a support hearing at least one layer of a light-sensitive silver halide emulsion containing a compound of the general formula:
where each of R1 and R2 is a group selected from the class consisting of hydrogen atoms, hydrocarbon groups, amino-, nitro-, hydroxy-, alkoxy-, oxyalkyl-, sulfonic-, carboxylic-, and halogensubstituted hydrocarbon groups and heterocyclic groups,
5. A process of colour photography which comprises forming a reducible silver salt image in an emulsion layer of a photographic element which contains a compound of the general formula:
where each of R1 and R2 is a group selected from the class consisting of hydrogen atoms, hydrocarbon groups, amin0-, nitro-, hydroxy-, alkoxy-, oxyalky1-, sulfonic-, carboxylic-, and halogensubstituted hydrocarbon groups and heterocyclic groups, and developing said image with an aromatic primary amino developing agent.
6. A process of colour photography which comprises forming a reducible silver salt image in an emulsion layer of a photographic element which contains a compound of the general formula:
R1N---NR2 to C0 Ci where each of R1 and R2 is a group selected from the class consisting of hydrogen atoms, hydrocarbon groups, amino-, nitro-, hydroxy-, alkoxy-, oxyalkyl-, sulfonic-, carboxylic-, and halogensubstituted hydrocarbon groups and heterocyclic groups, and developing said image with an N,N- dialkyl-p-phenylene diamine.
7. A process of colour photography which comprises forming a reducible silver salt image in an emulsion layer of a photographic element which includes, adjacent thereto, a layer containing a compound of the general formula:
where each of R1 and R2 is a group selected from the class consisting of hydrogen atoms, hydrocarbon groups, amino-, nitro-, hydroxy-, alkoxy-, oxya1kyl-, sulfonic-, carboxylic-, and halogensubstituted hydrocarbon groups and heterocyclic groups, and developing said image with an aromatic primary amino developing agent.
8. A process of colour photography which comprises forming a reducible silver salt; image in an emulsion layer of a photographic element which includes, adjacent thereto, a layer containing a compound of the general formula:
where each of R1 and R2 is a group selected from the class consisting of hydrogen atoms, hydrocarbon groups, amino-, nitro-, hydroxy-, alkoXy-, oxyalkyl-, sulfonic-, carboxylic-, and halogensubstituted hydrocarbon groups and heterocyclic groups, and developing said image with an N,N- dialkyl-p-phenylene diamine.
JOHN DAVID KENDALL.
DOUGLAS JAMES FRY.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9091/44A GB577260A (en) | 1944-05-12 | 1944-05-12 | Improvements in or relating to colour photography |
Publications (1)
Publication Number | Publication Date |
---|---|
US2427911A true US2427911A (en) | 1947-09-23 |
Family
ID=9865174
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US591830A Expired - Lifetime US2427911A (en) | 1944-05-12 | 1945-05-03 | 3, 5-diketo pyrazolidine color formers |
Country Status (2)
Country | Link |
---|---|
US (1) | US2427911A (en) |
GB (1) | GB577260A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2569418A (en) * | 1948-07-09 | 1951-09-25 | Gen Aniline & Film Corp | 3-azo derivatives of 1-substituted 2, 5-diketo-7-methylpyrimidopyrazoles |
US2674600A (en) * | 1954-04-06 | Derivatives of j | ||
US2745783A (en) * | 1950-11-06 | 1956-05-15 | Geigy Ag J R | Substituted 1. 2-diphenyl-3. 5-dioxo-pyrazolidines |
US2790807A (en) * | 1957-04-30 | Certain carbethoxy derivatives of | ||
US2801254A (en) * | 1955-07-25 | 1957-07-30 | Eastman Kodak Co | 1-phenyl-3, 5-pyrazolidinediones as antioxidants for fats and oils |
US2909465A (en) * | 1952-09-18 | 1959-10-20 | Knoll Ag | 1, 4-diphenyl-3, 5-diketo pyrazolidine compounds and compositions |
US3062806A (en) * | 1959-08-07 | 1962-11-06 | Geigy Ag J R | 1:2-metal complexes of monoazo dyes containing a 1, 2-diphenyl-3, 5-diketopyrazolidine coupling component |
US3250782A (en) * | 1961-09-21 | 1966-05-10 | Sandoz Ltd | Pyrazolidine-3, 5-dione derivatives |
US3379533A (en) * | 1963-06-10 | 1968-04-23 | Eastman Kodak Co | Dyes derived from 1, 2-disubstituted-3, 5-pyrazolidinediones and photographic elements containing such dyes |
US6210447B1 (en) * | 1996-03-22 | 2001-04-03 | L'oreal | Compositions containing pyrazolin-3,5-dione couplers for use in keratin fiber dyeing methods and kits |
-
1944
- 1944-05-12 GB GB9091/44A patent/GB577260A/en not_active Expired
-
1945
- 1945-05-03 US US591830A patent/US2427911A/en not_active Expired - Lifetime
Non-Patent Citations (1)
Title |
---|
None * |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2674600A (en) * | 1954-04-06 | Derivatives of j | ||
US2790807A (en) * | 1957-04-30 | Certain carbethoxy derivatives of | ||
US2569418A (en) * | 1948-07-09 | 1951-09-25 | Gen Aniline & Film Corp | 3-azo derivatives of 1-substituted 2, 5-diketo-7-methylpyrimidopyrazoles |
US2745783A (en) * | 1950-11-06 | 1956-05-15 | Geigy Ag J R | Substituted 1. 2-diphenyl-3. 5-dioxo-pyrazolidines |
US2909465A (en) * | 1952-09-18 | 1959-10-20 | Knoll Ag | 1, 4-diphenyl-3, 5-diketo pyrazolidine compounds and compositions |
US2801254A (en) * | 1955-07-25 | 1957-07-30 | Eastman Kodak Co | 1-phenyl-3, 5-pyrazolidinediones as antioxidants for fats and oils |
US3062806A (en) * | 1959-08-07 | 1962-11-06 | Geigy Ag J R | 1:2-metal complexes of monoazo dyes containing a 1, 2-diphenyl-3, 5-diketopyrazolidine coupling component |
US3250782A (en) * | 1961-09-21 | 1966-05-10 | Sandoz Ltd | Pyrazolidine-3, 5-dione derivatives |
US3379533A (en) * | 1963-06-10 | 1968-04-23 | Eastman Kodak Co | Dyes derived from 1, 2-disubstituted-3, 5-pyrazolidinediones and photographic elements containing such dyes |
US6210447B1 (en) * | 1996-03-22 | 2001-04-03 | L'oreal | Compositions containing pyrazolin-3,5-dione couplers for use in keratin fiber dyeing methods and kits |
US6551360B2 (en) * | 1996-03-22 | 2003-04-22 | Laurent Vidal | Pyrazoline-3,5-dione-containing compositions for dyeing keratin fibres; their use in dyeing as couplers; dyeing process |
Also Published As
Publication number | Publication date |
---|---|
GB577260A (en) | 1946-05-10 |
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