US2441491A - Cyanacetylamino phenol color formers for color photography - Google Patents
Cyanacetylamino phenol color formers for color photography Download PDFInfo
- Publication number
- US2441491A US2441491A US591828A US59182845A US2441491A US 2441491 A US2441491 A US 2441491A US 591828 A US591828 A US 591828A US 59182845 A US59182845 A US 59182845A US 2441491 A US2441491 A US 2441491A
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- United States
- Prior art keywords
- colour
- cyanacetylamino
- color
- group
- phenol
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- Expired - Lifetime
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- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 title description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 14
- 238000000034 method Methods 0.000 description 14
- 230000008569 process Effects 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 13
- 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 11
- 239000003795 chemical substances by application Substances 0.000 description 8
- 239000000839 emulsion Substances 0.000 description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 239000000975 dye Substances 0.000 description 6
- 125000005843 halogen group Chemical group 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 239000004332 silver Substances 0.000 description 5
- 229910052709 silver Inorganic materials 0.000 description 5
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 4
- -1 amino naphthols Chemical class 0.000 description 4
- 238000005859 coupling reaction Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- ZIUSEGSNTOUIPT-UHFFFAOYSA-N ethyl 2-cyanoacetate Chemical compound CCOC(=O)CC#N ZIUSEGSNTOUIPT-UHFFFAOYSA-N 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- WTEVQBCEXWBHNA-YFHOEESVSA-N neral Chemical compound CC(C)=CCC\C(C)=C/C=O WTEVQBCEXWBHNA-YFHOEESVSA-N 0.000 description 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- KJTXCKZBFHBRQT-UHFFFAOYSA-N 2-amino-5-ethoxyphenol Chemical compound CCOC1=CC=C(N)C(O)=C1 KJTXCKZBFHBRQT-UHFFFAOYSA-N 0.000 description 1
- HCPJEHJGFKWRFM-UHFFFAOYSA-N 2-amino-5-methylphenol Chemical compound CC1=CC=C(N)C(O)=C1 HCPJEHJGFKWRFM-UHFFFAOYSA-N 0.000 description 1
- 229940018563 3-aminophenol Drugs 0.000 description 1
- XBTWVJKPQPQTDW-UHFFFAOYSA-N 4-n,4-n-diethyl-2-methylbenzene-1,4-diamine Chemical compound CCN(CC)C1=CC=C(N)C(C)=C1 XBTWVJKPQPQTDW-UHFFFAOYSA-N 0.000 description 1
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- WTEVQBCEXWBHNA-JXMROGBWSA-N citral A Natural products CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 150000008049 diazo compounds Chemical class 0.000 description 1
- 150000002085 enols Chemical class 0.000 description 1
- 230000008570 general process Effects 0.000 description 1
- 239000001046 green dye Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 238000011065 in-situ storage Methods 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
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- KOOMFXGDLMRWSN-UHFFFAOYSA-N n-phenylnitrous amide Chemical compound O=NNC1=CC=CC=C1 KOOMFXGDLMRWSN-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000004060 quinone imines Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000008096 xylene 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
Definitions
- This invention relates to colour photography and particularly to dyestuff intermediates for use in colour photographic processes.
- colour-formers compounds, generally known as colour-formers" or colourcouplers, which couple with theoxidation products of such developers, formed during development, to form quinone-imine or azomethine dyes.
- the colour-couplers may be present in the developing solution employed, or may be included in a photographic emulsion layer which contains the reducible silver 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 diamine or its N.N.-dialkyl derivatives, e. g. N.N.-dimethyl and N.N.-diethyl p-ph'enylene diamines, or a homologue, e. g. 5-diethylamino-2- amino-toluene.
- ja'process of colour photography comprises developing a reducible silver. salt image by means of an aro-v matic primary amino developing agent in the presence of a cyanaetylamino phenol of the general formula:
- Such compounds may be prepared by reacting together an aminophenol (or naphthol or higher homologous compound) 'which is unsubstituted in' the para position tothe hydroxy group, or contains i a carboxyLsulphonic, halogen or other easily removable atom'or group in such position, with ethyl cyanacetate.
- an aminophenol or naphthol or higher homologous compound
- cyanacet-o-hydroxy-anilide may be prepared from o-amino-phenol and 'ethylcyanacetate in hot xylene solution in the presence of piperidine or other base. The'product separates on cooling, and after purification has a melting point of 178" 0.
- amino phenols and ,amino naphthols which may be similarly employed as initial reagents .are; for example, m-amino-phenol, 3- amino-e-naphthol, ,2-amino-5-ethoxy phenol, 2- amino-3-methyl 'phenol and 2-amino-5-chlor ph'enol. 1
- Particular compounds which may be employed arez' 1-cyanacetylamino-2ehydroxy-l-ethoxy benzene 2-cyan'acetylamino l-hydroxy naphthalene I-cyanacetyIaminO-2-hydroxy-6-methyl benzene These compounds are made by the general process described above, using the appropriate reagents.
- the benzene, naphthalene or other ring system present may'contain other substituent groups, e; g. hydrocarbon groups or alkoxy groups.
- the colour-couplers of this invention maybe included in a developing solution containin an aromatic primary amino developing agent, 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 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 areducible silver salt i a e by the usual ble hin techni ue;
- colour photographic processes in which the dye is formed by the coupling of the colourcouplers of the invention with the endatienprednets of an aromatic primary amino developing agent formed in situ during the deyeiopment, of a reducible silver salt image, ;th'e colours-couplers of the invention may also be employed in other colour photographic processes, ,e, g, .processesin which the dye is formed by direct coupling between the colour-coupler and a nitroso aniline, e. g. penitroso dialkyl aniline, or between the colour-coupler and a diazo compound.
- a nitroso aniline e. g. penitroso dialkyl aniline
- opin age trermin an a omethi idyeimase .situ with t e dev lop dsi er ima e, the esidua o o ler c p d it .;.a diet-to compound ppl di ution, t the ph tos arms el ment and t e n l az meth ne .de image bleached out, eavi only he az .dyeuiinage n the layer.
- a process of colour photography which comprises developing a reducible silver salt in a pho tographic element by means ore solution of an aromatic primary amino developing agent containing a compoundei t g neral o mu V NH.CO.CH2.CN
- a photographic element for colour photography which comprises a support bearing at least one layer of a light-sensitive silver halide emulsign and, adjacent thereto, a layer containing a compound of the general formula:
- hydroxy group is in a position taken frorn the group consisting of ortho and meta positions to the cyanacetylamino group and where X para to the hydroxy group and is a member selected from the class consisting .of the ydrogen 'andhalo en atoms and su phonic and carboxyl groups.
- v p i v V .5 A proeess'o colour ph t g aphy which comprises forming a reducible silver salt image in an emulsion layer of .a photographic element which contains a, compound oi the general formula:
- hydroxy group is in a position taken from the group consisting of ortho and meta positions to the cyanacetylamino group and where X s para to the hydroxy group and is a member selected from the classiconsisting of the hydrogen and halogen atoms and sulphonic and carboxyl 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:
- hydroxy group is in a position taken from the group consisting of ortho and meta positions to the cyanacetylamino group and where X is para to the hydroxy group and is a member selected from the class consisting of the hydrogen and halogenatoms and sulphonic and carboxyl groups, and developing said image with an -N,N-dialky1-p-phenylene diamine.
- i i 7 A process of colour photography which com prises forming a reducible silver salt image in an emulsionilayer of a photographic element which includes, adjacent thereto, a layer containing a compound of the general formula:
- amino developing agent -(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethy
- a process of colour photography which comprises torming a reducible silver salt image in an emulsion layer of a photographic element which includes, adjacent thereto, a layer containing a com ound of the general formula:
- hydroxy group is in a. position taken from the group consisting of ortho and meta positions to the cyanacetylamino group and where X is para to the hydroxy group and is a member selected from the class consisting of the hydrogen and halogen atoms and sulphonic and carboxyl groups, and developing said image with an N,N-dialkyl-p-phenylene diamine.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Patented May 11, 1948 CYANAGETYLAMINO PHENOL COLOR FORM- ERS FOR COLOR PHOTOGRAPHY John David Kendall and Douglas James-Fry, Ilford, England, assignors to Ilford Limited, Ilford, England, a British-companyv No Drawing. Application May 3, 1945, Serial No.
591,828. In Great Britain May 12, V
8 Claims.
1 p This invention relates to colour photography and particularly to dyestuff intermediates for use in colour photographic processes.
Processes of colour. photography are well known in which coloured images are produced by the development of reducible silver salt images by means of aromaticprimary amino develop-' ing agents in the presence of compounds, generally known as colour-formers" or colourcouplers, which couple with theoxidation products of such developers, formed during development, to form quinone-imine or azomethine dyes. The colour-couplers may be present in the developing solution employed, or may be included in a photographic emulsion layer which contains the reducible silver 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 diamine or its N.N.-dialkyl derivatives, e. g. N.N.-dimethyl and N.N.-diethyl p-ph'enylene diamines, or a homologue, 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 itis desired to include it, and where it is included ina photographic layer, neither it nor the dye derived from it must have any substantial tendency to diffuse from such layer, either into adjacent layers of the photographic element, or into processing baths. Moreover, it must be selected so that thecolourTof the dye obtained from it issuitable for the particular colour process with which it is intended to be used. 4
According to the present invention ja'process of colour photography comprises developing a reducible silver. salt image by means of an aro-v matic primary amino developing agent in the presence of a cyanaetylamino phenol of the general formula:
phonic, carboxyl, or halogen (or other atom or group readily removed during the dye-coupling reaction), or in the presence of a correspondin naphthol or higher homologous compound.
7 Such compoundsmay be prepared by reacting together an aminophenol (or naphthol or higher homologous compound) 'which is unsubstituted in' the para position tothe hydroxy group, or contains i a carboxyLsulphonic, halogen or other easily removable atom'or group in such position, with ethyl cyanacetate. Thus, for example, cyanacet-o-hydroxy-anilide may be prepared from o-amino-phenol and 'ethylcyanacetate in hot xylene solution in the presence of piperidine or other base. The'product separates on cooling, and after purification has a melting point of 178" 0. Similarly, using 2-amino-5-methyl phenol, the compound cyan'acet-o-h'ydroxy-p-toluidine, M.Pt. 189 C., is obtained. Both these compounds yield deep blue to blue-green dyes on colour-coupling development in accordance with thisinvention. Y
Other amino phenols and ,amino naphthols which may be similarly employed as initial reagents .are; for example, m-amino-phenol, 3- amino-e-naphthol, ,2-amino-5-ethoxy phenol, 2- amino-3-methyl 'phenol and 2-amino-5-chlor ph'enol. 1
Particular compounds which may be employed arez' 1-cyanacetylamino-2ehydroxy-l-ethoxy benzene 2-cyan'acetylamino l-hydroxy naphthalene I-cyanacetyIaminO-2-hydroxy-6-methyl benzene These compounds are made by the general process described above, using the appropriate reagents.
As will be clear from the foregoing discussion of the compounds, the benzene, naphthalene or other ring system present may'contain other substituent groups, e; g. hydrocarbon groups or alkoxy groups. 1 The colour-couplers of this invention maybe included in a developing solution containin an aromatic primary amino developing agent, 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 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 areducible silver salt i a e by the usual ble hin techni ue;
Although this invention is primarily concerned with colour photographic processes in which the dye is formed by the coupling of the colourcouplers of the invention with the endatienprednets of an aromatic primary amino developing agent formed in situ during the deyeiopment, of a reducible silver salt image, ;th'e colours-couplers of the invention may also be employed in other colour photographic processes, ,e, g, .processesin which the dye is formed by direct coupling between the colour-coupler and a nitroso aniline, e. g. penitroso dialkyl aniline, or between the colour-coupler and a diazo compound. As an examp e f. t s latter time Qf.- processes 9191. 1:- up er m be P s nt in a layer so aim-nee e bl si e t ima e, s ch mage .1: oped w th ar mat c p imary i lino dev. opin age trermin an a omethi idyeimase .situ with t e dev lop dsi er ima e, the esidua o o ler c p d it .;.a diet-to compound ppl di ution, t the ph tos arms el ment and t e n l az meth ne .de image bleached out, eavi only he az .dyeuiinage n the layer.
What-We claim 7 V 1. A process of c lour photegraphy which coinprises developing a, redlleibie silver salt image in a photograph c elementby means of. an arsomatie p imary amine eerelep ng a enti the presence of a c mpound oi v-thesenerel formul where the hydroxy group in a position taken from the group consisting of ortho and meta positions to the cyanacetylaminogroup andwhere ;X. is para to the hydroxy group and, is a member se, lected from the class consisting of the hydrogen and halogen atoms and 'sulphonic and carboxyl groups. I r .l 2, A process of colour photography which comprises developing a reducible silver salt in a pho tographic element by means ore solution of an aromatic primary amino developing agent containing a compoundei t g neral o mu V NH.CO.CH2.CN
from the group consisting of ortho and meta positions to the cyanacetylamino group and where X is para to the hydroxy group and is a member selected from the class consisting of the, hydrogen and halogen atoms and-sulphonic ande r ox l g ups. 1
4. A photographic element for colour photography which comprises a support bearing at least one layer of a light-sensitive silver halide emulsign and, adjacent thereto, a layer containing a compound of the general formula:
NH.OO.CH2.CN
where the hydroxy group is in a position taken frorn the group consisting of ortho and meta positions to the cyanacetylamino group and where X para to the hydroxy group and is a member selected from the class consisting .of the ydrogen 'andhalo en atoms and su phonic and carboxyl groups. v p i v V .5 A proeess'o colour ph t g aphy which comprises forming a reducible silver salt image in an emulsion layer of .a photographic element which contains a, compound oi the general formula:
where the hydroxy group is in a position taken from the group consisting of ortho and meta positions to the cyanacetylamino group and where X s para to the hydroxy group and is a member selected from the classiconsisting of the hydrogen and halogen atoms and sulphonic and carboxyl 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:
where the hydroxy group is in a position taken from the group consisting of ortho and meta positions to the cyanacetylamino group and where X is para to the hydroxy group and is a member selected from the class consisting of the hydrogen and halogenatoms and sulphonic and carboxyl groups, and developing said image with an -N,N-dialky1-p-phenylene diamine. i i 7. A process of colour photography which com prises forming a reducible silver salt image in an emulsionilayer of a photographic element which includes, adjacent thereto, a layer containing a compound of the general formula:
' ATNHD 0.0Hz.CN
where the hydroxy group is in a position taken from the group consisting of ortho and meta positions to the cyanacetylamino group and where X is para to the hydroxy group and is a memberseleoted from the class consisting of the hydrogen and halogen atoms and sulphonic and carboxyl groups, and developing said image with an aromatic primary. amino developing agent,-
8. A process of colour photography which comprises torming a reducible silver salt image in an emulsion layer of a photographic element which includes, adjacent thereto, a layer containing a com ound of the general formula:
NH.CO.CH1.CN
where the hydroxy group is in a. position taken from the group consisting of ortho and meta positions to the cyanacetylamino group and where X is para to the hydroxy group and is a member selected from the class consisting of the hydrogen and halogen atoms and sulphonic and carboxyl groups, and developing said image with an N,N-dialkyl-p-phenylene diamine.
JOHN DAVID KENDALL. DOUGLAS'JAMES FRY.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9088/44A GB576891A (en) | 1944-05-12 | 1944-05-12 | Improvements in or relating to colour photography |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2441491A true US2441491A (en) | 1948-05-11 |
Family
ID=9865125
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US591828A Expired - Lifetime US2441491A (en) | 1944-05-12 | 1945-05-03 | Cyanacetylamino phenol color formers for color photography |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US2441491A (en) |
| GB (1) | GB576891A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2507180A (en) * | 1947-02-08 | 1950-05-09 | Eastman Kodak Co | Cyano acetamino color couplers |
| US2525503A (en) * | 1946-01-10 | 1950-10-10 | Gen Aniline & Film Corp | Production of phenazonium dyestuff images |
| US2536010A (en) * | 1947-07-11 | 1950-12-26 | Gen Aniline & Film Corp | Preparation of azine dyestuff images |
| US2595768A (en) * | 1948-09-07 | 1952-05-06 | Ilford Ltd | Photographic color correction |
| DE1041357B (en) * | 1957-07-31 | 1958-10-16 | Agfa Ag | Process and multilayer material for the production of yellow dye images by color development |
| US3909190A (en) * | 1972-08-21 | 1975-09-30 | Henkel & Cie Gmbh | Hair dyeing process and composition containing {60 -cyano-methanesulfonamido-nitrobenzene derivatives |
Citations (11)
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|---|---|---|---|---|
| US2108602A (en) * | 1935-03-21 | 1938-02-15 | Eastman Kodak Co | Photographic color-forming compounds |
| US2133937A (en) * | 1937-02-15 | 1938-10-18 | Du Pont Film Mfg Corp | Color photography |
| US2181944A (en) * | 1936-11-26 | 1939-12-05 | Agfa Ansco Corp | Production of black-and-white photographic pictures |
| US2220908A (en) * | 1938-04-04 | 1940-11-12 | Ilford Ltd | Production of colored photographic images by color development |
| US2269481A (en) * | 1938-08-03 | 1942-01-13 | Ilford Ltd | Production of colored photographic images |
| US2303380A (en) * | 1937-08-06 | 1942-12-01 | American Mach & Foundry | Sewing apparatus |
| US2328652A (en) * | 1941-04-18 | 1943-09-07 | Du Pont | Process of color photography and composition thereof |
| US2350380A (en) * | 1940-08-01 | 1944-06-06 | Du Pont | Photography |
| US2367531A (en) * | 1942-06-12 | 1945-01-16 | Eastman Kodak Co | Acylaminophenol photographic couplers |
| US2369929A (en) * | 1943-03-18 | 1945-02-20 | Eastman Kodak Co | Acylamino phenol couplers |
| US2380809A (en) * | 1939-12-11 | 1945-07-31 | Verkinderen Honore | Color couplers for photographic color development |
-
1944
- 1944-05-12 GB GB9088/44A patent/GB576891A/en not_active Expired
-
1945
- 1945-05-03 US US591828A patent/US2441491A/en not_active Expired - Lifetime
Patent Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2108602A (en) * | 1935-03-21 | 1938-02-15 | Eastman Kodak Co | Photographic color-forming compounds |
| US2181944A (en) * | 1936-11-26 | 1939-12-05 | Agfa Ansco Corp | Production of black-and-white photographic pictures |
| US2133937A (en) * | 1937-02-15 | 1938-10-18 | Du Pont Film Mfg Corp | Color photography |
| US2303380A (en) * | 1937-08-06 | 1942-12-01 | American Mach & Foundry | Sewing apparatus |
| US2220908A (en) * | 1938-04-04 | 1940-11-12 | Ilford Ltd | Production of colored photographic images by color development |
| US2269481A (en) * | 1938-08-03 | 1942-01-13 | Ilford Ltd | Production of colored photographic images |
| US2380809A (en) * | 1939-12-11 | 1945-07-31 | Verkinderen Honore | Color couplers for photographic color development |
| US2350380A (en) * | 1940-08-01 | 1944-06-06 | Du Pont | Photography |
| US2328652A (en) * | 1941-04-18 | 1943-09-07 | Du Pont | Process of color photography and composition thereof |
| US2367531A (en) * | 1942-06-12 | 1945-01-16 | Eastman Kodak Co | Acylaminophenol photographic couplers |
| US2369929A (en) * | 1943-03-18 | 1945-02-20 | Eastman Kodak Co | Acylamino phenol couplers |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2525503A (en) * | 1946-01-10 | 1950-10-10 | Gen Aniline & Film Corp | Production of phenazonium dyestuff images |
| US2507180A (en) * | 1947-02-08 | 1950-05-09 | Eastman Kodak Co | Cyano acetamino color couplers |
| US2536010A (en) * | 1947-07-11 | 1950-12-26 | Gen Aniline & Film Corp | Preparation of azine dyestuff images |
| US2595768A (en) * | 1948-09-07 | 1952-05-06 | Ilford Ltd | Photographic color correction |
| DE1041357B (en) * | 1957-07-31 | 1958-10-16 | Agfa Ag | Process and multilayer material for the production of yellow dye images by color development |
| US3909190A (en) * | 1972-08-21 | 1975-09-30 | Henkel & Cie Gmbh | Hair dyeing process and composition containing {60 -cyano-methanesulfonamido-nitrobenzene derivatives |
Also Published As
| Publication number | Publication date |
|---|---|
| GB576891A (en) | 1946-04-25 |
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