GB826493A - A method of making masked photographic images - Google Patents
A method of making masked photographic imagesInfo
- Publication number
- GB826493A GB826493A GB25722/56A GB2572256A GB826493A GB 826493 A GB826493 A GB 826493A GB 25722/56 A GB25722/56 A GB 25722/56A GB 2572256 A GB2572256 A GB 2572256A GB 826493 A GB826493 A GB 826493A
- Authority
- GB
- United Kingdom
- Prior art keywords
- pyrazolone
- phenyl
- chloride
- sulphobenzamido
- tert
- 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
- 238000004519 manufacturing process Methods 0.000 title 1
- -1 3 - sulphobenzamido Chemical group 0.000 abstract 7
- 230000008878 coupling Effects 0.000 abstract 4
- 238000010168 coupling process Methods 0.000 abstract 4
- 238000005859 coupling reaction Methods 0.000 abstract 4
- 238000010438 heat treatment Methods 0.000 abstract 4
- AKRCTRQPMBWUTK-UHFFFAOYSA-M 3-pentoxycarbonylnaphthalene-2-diazonium chloride Chemical compound [Cl-].C(CCCC)OC(=O)C1=CC2=CC=CC=C2C=C1[N+]#N AKRCTRQPMBWUTK-UHFFFAOYSA-M 0.000 abstract 2
- PVKNQGWSRAGMNM-UHFFFAOYSA-N 5-amino-2-phenyl-1h-pyrazol-3-one Chemical compound N1C(N)=CC(=O)N1C1=CC=CC=C1 PVKNQGWSRAGMNM-UHFFFAOYSA-N 0.000 abstract 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 abstract 2
- HHBASJKMAJKMNN-UHFFFAOYSA-N benzoyl chloride;sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O.ClC(=O)C1=CC=CC=C1 HHBASJKMAJKMNN-UHFFFAOYSA-N 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 230000003301 hydrolyzing effect Effects 0.000 abstract 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 1
- SDZMCSYBOPYKCP-UHFFFAOYSA-N 2-[[4-[(2-dodecoxyphenyl)diazenyl]-5-oxo-1-phenyl-4H-pyrazol-3-yl]carbamoyl]benzoic acid Chemical compound C1(=CC=CC=C1)N1N=C(C(C1=O)N=NC1=C(C=CC=C1)OCCCCCCCCCCCC)NC(C1=C(C=CC=C1)C(=O)O)=O SDZMCSYBOPYKCP-UHFFFAOYSA-N 0.000 abstract 1
- XFXOLBNQYFRSLQ-UHFFFAOYSA-N 3-amino-2-naphthoic acid Chemical compound C1=CC=C2C=C(C(O)=O)C(N)=CC2=C1 XFXOLBNQYFRSLQ-UHFFFAOYSA-N 0.000 abstract 1
- KHXUUPPXJWVTHH-UHFFFAOYSA-M 4-methoxybenzenediazonium;chloride Chemical compound [Cl-].COC1=CC=C([N+]#N)C=C1 KHXUUPPXJWVTHH-UHFFFAOYSA-M 0.000 abstract 1
- UXICFQHPMBCLCN-UHFFFAOYSA-M 4-octadecoxybenzenediazonium chloride Chemical compound [Cl-].C(CCCCCCCCCCCCCCCCC)OC1=CC=C(C=C1)[N+]#N UXICFQHPMBCLCN-UHFFFAOYSA-M 0.000 abstract 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 abstract 1
- NUWYUFIOOWDUHS-UHFFFAOYSA-M [Cl-].C(CCCCCCCCCCC)OC1=CC=C(C=C1)[N+]#N Chemical compound [Cl-].C(CCCCCCCCCCC)OC1=CC=C(C=C1)[N+]#N NUWYUFIOOWDUHS-UHFFFAOYSA-M 0.000 abstract 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 abstract 1
- 238000006193 diazotization reaction Methods 0.000 abstract 1
- RMHJJUOPOWPRBP-UHFFFAOYSA-N naphthalene-1-carboxamide Chemical compound C1=CC=C2C(C(=O)N)=CC=CC2=C1 RMHJJUOPOWPRBP-UHFFFAOYSA-N 0.000 abstract 1
- QHDYIMWKSCJTIM-UHFFFAOYSA-N phenyl 1-hydroxynaphthalene-2-carboxylate Chemical compound C1=CC2=CC=CC=C2C(O)=C1C(=O)OC1=CC=CC=C1 QHDYIMWKSCJTIM-UHFFFAOYSA-N 0.000 abstract 1
- WSDQIHATCCOMLH-UHFFFAOYSA-N phenyl n-(3,5-dichlorophenyl)carbamate Chemical compound ClC1=CC(Cl)=CC(NC(=O)OC=2C=CC=CC=2)=C1 WSDQIHATCCOMLH-UHFFFAOYSA-N 0.000 abstract 1
- RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 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
- 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
- G03C7/333—Coloured coupling substances, e.g. for the correction of the coloured image
- G03C7/3335—Coloured coupling substances, e.g. for the correction of the coloured image containing an azo chromophore
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US536502A US2848326A (en) | 1955-09-26 | 1955-09-26 | Method for preparing masked images |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB826493A true GB826493A (en) | 1960-01-06 |
Family
ID=24138760
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB25722/56A Expired GB826493A (en) | 1955-09-26 | 1956-08-23 | A method of making masked photographic images |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US2848326A (enrdf_load_stackoverflow) |
| BE (1) | BE551200A (enrdf_load_stackoverflow) |
| FR (1) | FR1161137A (enrdf_load_stackoverflow) |
| GB (1) | GB826493A (enrdf_load_stackoverflow) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3127268A (en) * | 1964-03-31 | Hellmig | ||
| US3135609A (en) * | 1960-06-29 | 1964-06-02 | Gen Aniline & Film Corp | 1-hydroxy-2-naphthamide couplers for color photography |
| BE605204A (enrdf_load_stackoverflow) * | 1961-06-21 | |||
| US3233532A (en) * | 1962-04-25 | 1966-02-08 | Minnesota Mining & Mfg | Photographic apparatus |
| US3411905A (en) * | 1965-06-14 | 1968-11-19 | Eastman Kodak Co | Photographic masking process |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB503824A (en) * | 1936-07-07 | 1939-04-11 | Kodak Ltd | Process of colour photography |
| US2306410A (en) * | 1936-07-07 | 1942-12-29 | Eastman Kodak Co | Color development |
| US2350380A (en) * | 1940-08-01 | 1944-06-06 | Du Pont | Photography |
-
0
- BE BE551200D patent/BE551200A/xx unknown
-
1955
- 1955-09-26 US US536502A patent/US2848326A/en not_active Expired - Lifetime
-
1956
- 1956-08-23 GB GB25722/56A patent/GB826493A/en not_active Expired
- 1956-09-25 FR FR1161137D patent/FR1161137A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| US2848326A (en) | 1958-08-19 |
| FR1161137A (fr) | 1958-08-21 |
| BE551200A (enrdf_load_stackoverflow) |
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