GB795476A - Process for the production of photographic colour images by colour development - Google Patents
Process for the production of photographic colour images by colour developmentInfo
- Publication number
- GB795476A GB795476A GB19856/55A GB1985655A GB795476A GB 795476 A GB795476 A GB 795476A GB 19856/55 A GB19856/55 A GB 19856/55A GB 1985655 A GB1985655 A GB 1985655A GB 795476 A GB795476 A GB 795476A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- aminopyrazoline
- dihydrochloride
- sulphophenyl
- pyrazolone
- 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
- 238000000034 method Methods 0.000 title 1
- -1 sulpho groups Chemical group 0.000 abstract 5
- 239000003795 chemical substances by application Substances 0.000 abstract 3
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 abstract 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 abstract 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 abstract 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 abstract 2
- UQRQFLMLMSIRPO-UHFFFAOYSA-N 2-(4-aminophenyl)-1,3-dihydropyrazol-5-amine Chemical compound N1C(N)=CCN1C1=CC=C(N)C=C1 UQRQFLMLMSIRPO-UHFFFAOYSA-N 0.000 abstract 1
- FRMFNXXDJIHFAX-UHFFFAOYSA-N 4-(3-heptadecyl-5-oxo-4h-pyrazol-1-yl)benzenesulfonic acid Chemical compound O=C1CC(CCCCCCCCCCCCCCCCC)=NN1C1=CC=C(S(O)(=O)=O)C=C1 FRMFNXXDJIHFAX-UHFFFAOYSA-N 0.000 abstract 1
- 241001479434 Agfa Species 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 239000003086 colorant Substances 0.000 abstract 1
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 229910000027 potassium carbonate Inorganic materials 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 229910052709 silver Inorganic materials 0.000 abstract 1
- 239000004332 silver Substances 0.000 abstract 1
- 235000010265 sodium sulphite Nutrition 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 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
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/29—Development processes or agents therefor
- G03C5/30—Developers
- G03C5/3028—Heterocyclic compounds
- G03C5/3035—Heterocyclic compounds containing a diazole ring
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Plural Heterocyclic Compounds (AREA)
- Developing Agents For Electrophotography (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Abstract
795,476. Photographic colour development. AGFA AKT.-GES FUR PHOTOFABRIKATION. July 8, 1955 [July 8, 1954], No. 19856/55. Class 98(2) In photographic colour development, 1- (p - aminophenyl) - 3 - aminopyrazoline or a derivative thereof unsubstituted in both amino groups is used as the colour developing substance. The derivative may be one in which one or more hydrogen atoms in the 1 - phenyl nucleus are replaced by halogen atoms or by alkyl or substituted alkyl alkoxy, or sulpho groups. Derivatives specified are 1 - (4<SP>1</SP> - amino - 3<SP>1</SP> - methoxyphenyl)-, 1 (4<SP>1</SP> - amino - 3<SP>1</SP>-methylphenyl)-, 1 - (4<SP>1</SP> - amino - 2<SP>1</SP> - methylphenyl)-, 1 - (4<SP>1</SP> - amino, - 3<SP>1</SP> - # - hydroxyethylphenyl)-, and 1 - (4<SP>1</SP> - amino - 3' - # - carboxyethylphenyl) - 3 - aminopyrazoline dihydrochloride. In Example 1, an exposed silver halide emulsion containing 1 - (4<SP>1</SP> - sulphophenyl) - 3 - palmityl - 5 - pyrazolone is colour developed in 3 minutes to a gamma of 0.7 in a solution containing 1 - (p-aminophenyl) - 3 - aminopyrazolone dihydrochloride, potassium carbonate, potassium bromide and sodium sulphite, as contrasted with a time of 7 minutes to reach the same gamma in a colour developer containing 4 - amino - N - ethyl : N - # - hydroxyethylaniline. A table is given showing the difference in the colours obtained using the two colour developing agents and the following couplers: 4<SP>1</SP> - stearylaminobenzoylacet - 3 : 5 - dicarboxyanilide, 1 - p - sulphophenyl - 3 - heptadecyl.- 5 - pyrazolone, 1 - naphthol 4 - sulpho - 2 - N - octadecylnaphthamide, 4 - # - octadecylsuccinamylbenzoylacetonitrile, and 1 - p - sulphophenyl - 3 - (4<SP>1</SP> - stearylaminobenzamido) - 5 - pyrazolone. Similar data are given for the colour developing agents 1-(41-amino - 3' - methoxyphenyl) - 3 - aminopyrazoline and 1 - (4<SP>1</SP> amino - 2' - methylphenyl) - 3 - aminopyrazoline, both compared with 4 - amino - N - ethyl : N - # - hydroxyethylaniline, and the coupler 1 - p - sulphophenyl - 3 - heptadecyl - 5 - pyrazolone. In examples 2 to 7, the colour developing agent and the coupler are (2) 1 - (4<SP>1</SP> - amino - 31 - methoxyphenyl) - 3 - aminopyrazoline dihydrochloride and 1 - (4<SP>1</SP> - sulphophenyl) - 3 - palmityl - 5 - pyrazolone; (3) 1 - (41 - amino - 3<SP>1</SP> - chlorophenyl) - 3 - aminopyrazoline dihydrochloride and 1 - hydroxy - 4 - sulpho - 2 - naphthoyl - stearylamilide; (4) 1 - (4<SP>1</SP> - amino - 31 - methylphenyl) - 3 - aminopyrazoline dihydrochloride and 4<SP>1</SP> - stearylaminobenzoylacet - 3 : 5 - dicarboxyanilide; (5) 1 - (4<SP>1</SP> - amino - 2<SP>1</SP> - methylphenyl) - 3 - aminopyrazoline dihydrochloride and 4 - #-octadecylsuccinamylbenzoylacetonitrile; (6) 1 - (4<SP>1</SP> - amino - 3<SP>1</SP> - methoxyphenyl) - 3 - aminopyrazoline dihydrochloride and 1 - (4<SP>1</SP> - sulphophenyl) - 3 - palmityl - 5 - pyrazolone; and (7) 1 - (4<SP>1</SP> - amino - 3<SP>1</SP> - chlorophenyl) - 3 - aminopyrazoline dihydrochloride and 1 - hydroxy - 4 - sulpho - 2 - naphthoyl - stearylanilide. Specifications 757,840 and 776,322 [Group IV(b)] are referred to.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEA20693A DE955026C (en) | 1954-07-08 | 1954-07-08 | Process for producing colored images by color development |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB795476A true GB795476A (en) | 1958-05-21 |
Family
ID=6924750
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB19856/55A Expired GB795476A (en) | 1954-07-08 | 1955-07-08 | Process for the production of photographic colour images by colour development |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US2892714A (en) |
| BE (1) | BE539271A (en) |
| CH (1) | CH336259A (en) |
| DE (1) | DE955026C (en) |
| FR (1) | FR1126757A (en) |
| GB (1) | GB795476A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE611885A (en) * | 1960-12-24 | |||
| US3547646A (en) * | 1966-12-16 | 1970-12-15 | Keuffel & Esser Co | Light-sensitive imaging material containing hydrazones |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB542502A (en) * | 1940-07-10 | 1942-01-13 | John David Kendall | Improvements in or relating to photographic development processes |
| US2533514A (en) * | 1947-11-19 | 1950-12-12 | Eastman Kodak Co | Photographic emulsions containing color couplers and amide coupler solvents |
| DE875048C (en) * | 1950-04-06 | 1953-04-30 | Ilford Ltd | Process for the preparation of 3-pyrazolidones |
| DE870418C (en) * | 1950-04-06 | 1953-03-12 | Ilford Ltd | Process for the preparation of pyrazoline compounds |
-
0
- BE BE539271D patent/BE539271A/xx unknown
-
1954
- 1954-07-08 DE DEA20693A patent/DE955026C/en not_active Expired
-
1955
- 1955-06-15 CH CH336259D patent/CH336259A/en unknown
- 1955-06-28 FR FR1126757D patent/FR1126757A/en not_active Expired
- 1955-07-07 US US520608A patent/US2892714A/en not_active Expired - Lifetime
- 1955-07-08 GB GB19856/55A patent/GB795476A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BE539271A (en) | |
| CH336259A (en) | 1959-02-15 |
| DE955026C (en) | 1956-12-27 |
| FR1126757A (en) | 1956-11-30 |
| US2892714A (en) | 1959-06-30 |
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