GB651749A - Improvements in photographic developers - Google Patents
Improvements in photographic developersInfo
- Publication number
- GB651749A GB651749A GB6104/48A GB610448A GB651749A GB 651749 A GB651749 A GB 651749A GB 6104/48 A GB6104/48 A GB 6104/48A GB 610448 A GB610448 A GB 610448A GB 651749 A GB651749 A GB 651749A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethyl
- methylsulphonamidoethyl
- phenetidine
- prepared
- amino
- 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
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
-
- 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
- G03C7/407—Development processes or agents therefor
- G03C7/413—Developers
- G03C7/4136—Developers p-Phenylenediamine or derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
4 - Amino - N - ethyl : N - (b - methylsulphonamidoethyl) - m - phenetidine oxalate is prepared by reducing N-ethyl : N - (b - methylsulphonamidoethyl) - 4 - nitroso - m - phenetidine in absolute alcohol with hydrogen in presence of Raney Nickel, filtering off the catalyst, and adding oxalic acid. 4-Amino-n-methyl : N-(b -methylsulphonamidoethyl) - m - anisidine, 4-amino - N - ethyl : N - (b - methylsulphonamidoethyl) - m - anisidine, 4 - amino - 3 - propoxy - N - propyl : N - (b - methylsulphonamidoethyl) - aniline, 4 - amino - 3 - methoxy - 5-methyl - N - ethyl : N - (2 - methylsulphonamidoethyl) - aniline, and 4 - amino - 3 : 5 - diethoxy-N - ethyl : N - (b - methylsulphonamidoethyl)-aniline are similarly prepared. N - Ethyl - m - acetophenetidide is prepared by reacting m-phenetidine first with ethyl iodide and then with acetic anhydride. N - Ethyl - m - phenetidine is prepared by hydrolysing N - ethyl - m - acetophenetidide by boiling with aqueous HCl. N - (b - Aminoethyl) : N - ethyl - m - phenetidine is prepared by heating a mixture of N-ethyl - m - phenetidine and b - bromoethylamine hydrobromide. N - Ethyl : N - (b - methylsulphonamidoethyl)-m-phenetidine is prepared by reacting N-(b -aminoethyl) : N - ethyl - m - phenetidine with methanesulphonyl chloride. N - Ethyl : N - (b - methylsulphonamidoethyl)-4 - nitroso - m - phenetidine is prepared by adding sodium nitrite to an acidified solution of N - ethyl : N - (b - methylsulphonamidoethyl) - m - phenetidine. Specifications 2562/13, [Class 98 (ii)], 478,989, 493,952, [Group XX], and 536,577 are referred to.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US731420A US2548574A (en) | 1947-02-27 | 1947-02-27 | Sulfonamide substituted p-phenylenediamines containing o-alkoxy groups as silver halide photographic developers |
US82281A US2552240A (en) | 1947-02-27 | 1949-03-14 | N-beta-methylsulfonamidoethyl-p-phenylenediamines |
Publications (1)
Publication Number | Publication Date |
---|---|
GB651749A true GB651749A (en) | 1951-04-11 |
Family
ID=26767282
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB6104/48A Expired GB651749A (en) | 1947-02-27 | 1948-02-27 | Improvements in photographic developers |
Country Status (3)
Country | Link |
---|---|
US (2) | US2548574A (en) |
FR (1) | FR980375A (en) |
GB (1) | GB651749A (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2652428A (en) * | 1951-05-05 | 1953-09-15 | Eastman Kodak Co | N-alkyl-n-(beta-methylsulfonamidoethyl)-p-aminophenols |
US2739981A (en) * | 1952-08-26 | 1956-03-27 | American Home Prod | Diamines and salts thereof |
JPS5079132A (en) * | 1973-11-14 | 1975-06-27 | ||
DE2628999C2 (en) * | 1976-06-28 | 1987-03-26 | Henkel KGaA, 4000 Düsseldorf | Hair dye |
JPS5916261B2 (en) * | 1978-12-20 | 1984-04-14 | 富士写真フイルム株式会社 | Color image forming method |
DE3431860A1 (en) * | 1984-08-30 | 1986-03-06 | Agfa-Gevaert Ag, 5090 Leverkusen | METHOD FOR PRODUCING COLOR PHOTOGRAPHIC IMAGES |
GB9702194D0 (en) * | 1997-02-04 | 1997-03-26 | Lilly Co Eli | Sulphonide derivatives |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2039730A (en) * | 1935-02-27 | 1936-05-05 | Eastman Kodak Co | Color-forming developer |
US2241769A (en) * | 1939-03-29 | 1941-05-13 | Eastman Kodak Co | Sulphonic acid derivatives of aryl diamines |
US2193015A (en) * | 1939-05-24 | 1940-03-12 | Eastman Kodak Co | Developer containing sulphonamide groups |
GB541328A (en) * | 1940-02-19 | 1941-11-24 | Eastman Kodak Co | Improvements relating to the use of substituted aromatic diamines in photography |
FR956696A (en) * | 1941-08-08 | 1950-02-02 | ||
US2364350A (en) * | 1941-11-06 | 1944-12-05 | Eastman Kodak Co | Photographic developer |
US2374337A (en) * | 1943-03-04 | 1945-04-24 | Eastman Kodak Co | Arylene diamine compounds |
-
1947
- 1947-02-27 US US731420A patent/US2548574A/en not_active Expired - Lifetime
-
1948
- 1948-02-27 GB GB6104/48A patent/GB651749A/en not_active Expired
- 1948-02-27 FR FR980375D patent/FR980375A/en not_active Expired
-
1949
- 1949-03-14 US US82281A patent/US2552240A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US2548574A (en) | 1951-04-10 |
US2552240A (en) | 1951-05-08 |
FR980375A (en) | 1951-05-11 |
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