GB1235747A - Antifoggants for photographic products and processes - Google Patents
Antifoggants for photographic products and processesInfo
- Publication number
- GB1235747A GB1235747A GB58958/68A GB5895868A GB1235747A GB 1235747 A GB1235747 A GB 1235747A GB 58958/68 A GB58958/68 A GB 58958/68A GB 5895868 A GB5895868 A GB 5895868A GB 1235747 A GB1235747 A GB 1235747A
- Authority
- GB
- United Kingdom
- Prior art keywords
- prepared
- azabenzimidazole
- solution
- amino
- bromo
- 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
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 18
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 8
- QQXIHQFSQBHJTP-UHFFFAOYSA-N Cl.Cl.NC1=NC2=C(N=CN2)C=C1 Chemical compound Cl.Cl.NC1=NC2=C(N=CN2)C=C1 QQXIHQFSQBHJTP-UHFFFAOYSA-N 0.000 abstract 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 5
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 4
- 235000019253 formic acid Nutrition 0.000 abstract 4
- 238000010992 reflux Methods 0.000 abstract 4
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 abstract 4
- 239000001117 sulphuric acid Substances 0.000 abstract 4
- 235000011149 sulphuric acid Nutrition 0.000 abstract 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 abstract 3
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 3
- CRELZBHEKSIUDR-UHFFFAOYSA-N 5-bromo-6-methyl-3-nitropyridin-2-amine Chemical compound CC1=NC(N)=C([N+]([O-])=O)C=C1Br CRELZBHEKSIUDR-UHFFFAOYSA-N 0.000 abstract 2
- SEOZHXRTVJPQPZ-UHFFFAOYSA-N 5-bromo-6-methylpyridin-2-amine Chemical compound CC1=NC(N)=CC=C1Br SEOZHXRTVJPQPZ-UHFFFAOYSA-N 0.000 abstract 2
- XFHAYQGHHKCVBA-UHFFFAOYSA-N 5-bromo-6-methylpyridine-2,3-diamine Chemical compound CC1=NC(N)=C(N)C=C1Br XFHAYQGHHKCVBA-UHFFFAOYSA-N 0.000 abstract 2
- ZRCMCGQDIYNWDX-UHFFFAOYSA-N 5-chloropyridine-2,3-diamine Chemical compound NC1=CC(Cl)=CN=C1N ZRCMCGQDIYNWDX-UHFFFAOYSA-N 0.000 abstract 2
- ZZFKQUTYXXPQBS-UHFFFAOYSA-N 6-bromo-5-methyl-1h-imidazo[4,5-b]pyridine Chemical compound C1=C(Br)C(C)=NC2=C1NC=N2 ZZFKQUTYXXPQBS-UHFFFAOYSA-N 0.000 abstract 2
- XSLCKYZPGSZOQQ-UHFFFAOYSA-N 6-nitro-1H-imidazo[4,5-b]pyridin-5-amine Chemical compound [N+](=O)([O-])C=1C(=NC2=C(N=CN2)C1)N XSLCKYZPGSZOQQ-UHFFFAOYSA-N 0.000 abstract 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 abstract 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 2
- 229910052794 bromium Inorganic materials 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 239000003610 charcoal Substances 0.000 abstract 2
- 238000001816 cooling Methods 0.000 abstract 2
- 238000001704 evaporation Methods 0.000 abstract 2
- 230000005484 gravity Effects 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 229910017604 nitric acid Inorganic materials 0.000 abstract 2
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 abstract 2
- 229910003446 platinum oxide Inorganic materials 0.000 abstract 2
- OLOSAKLIEXRQST-UHFFFAOYSA-N pyridine-2,3,6-triamine;dihydrochloride Chemical compound Cl.Cl.NC1=CC=C(N)C(N)=N1 OLOSAKLIEXRQST-UHFFFAOYSA-N 0.000 abstract 2
- 235000010288 sodium nitrite Nutrition 0.000 abstract 2
- KTIHRQBDCJLDQX-UHFFFAOYSA-N 1,4-dihydroimidazo[4,5-b]pyridin-5-one Chemical compound N1C(=O)C=CC2=C1N=CN2 KTIHRQBDCJLDQX-UHFFFAOYSA-N 0.000 abstract 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 abstract 1
- GAMYYCRTACQSBR-UHFFFAOYSA-N 4-azabenzimidazole Chemical class C1=CC=C2NC=NC2=N1 GAMYYCRTACQSBR-UHFFFAOYSA-N 0.000 abstract 1
- INKJIWXVLWIENL-UHFFFAOYSA-N 5-bromo-1h-imidazo[4,5-b]pyridine Chemical compound BrC1=CC=C2NC=NC2=N1 INKJIWXVLWIENL-UHFFFAOYSA-N 0.000 abstract 1
- YRGMYJUKFJPNPD-UHFFFAOYSA-N 5-bromopyridine-2,3-diamine Chemical compound NC1=CC(Br)=CN=C1N YRGMYJUKFJPNPD-UHFFFAOYSA-N 0.000 abstract 1
- IANINCNCSTYFSO-UHFFFAOYSA-N 5-methyl-1h-imidazo[4,5-b]pyridine Chemical compound CC1=CC=C2NC=NC2=N1 IANINCNCSTYFSO-UHFFFAOYSA-N 0.000 abstract 1
- XPHWCAKVRKUXLK-UHFFFAOYSA-N 6-bromo-1h-imidazo[4,5-b]pyridine Chemical compound BrC1=CN=C2N=CNC2=C1 XPHWCAKVRKUXLK-UHFFFAOYSA-N 0.000 abstract 1
- ILPMNVPFPXMQAD-UHFFFAOYSA-N 6-chloro-1h-imidazo[4,5-b]pyridine Chemical compound ClC1=CN=C2N=CNC2=C1 ILPMNVPFPXMQAD-UHFFFAOYSA-N 0.000 abstract 1
- ZVIVLVMOMHEHIU-UHFFFAOYSA-N 6-chloro-2-methyl-1h-imidazo[4,5-b]pyridine Chemical compound C1=C(Cl)C=C2NC(C)=NC2=N1 ZVIVLVMOMHEHIU-UHFFFAOYSA-N 0.000 abstract 1
- QUXLCYFNVNNRBE-UHFFFAOYSA-N 6-methylpyridin-2-amine Chemical compound CC1=CC=CC(N)=N1 QUXLCYFNVNNRBE-UHFFFAOYSA-N 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 238000001914 filtration Methods 0.000 abstract 1
- 238000005984 hydrogenation reaction Methods 0.000 abstract 1
- 239000005457 ice water Substances 0.000 abstract 1
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 abstract 1
- DOOCXEFAMLFXHN-UHFFFAOYSA-N n-(1h-imidazo[4,5-b]pyridin-5-yl)methanesulfonamide Chemical compound CS(=O)(=O)NC1=CC=C2NC=NC2=N1 DOOCXEFAMLFXHN-UHFFFAOYSA-N 0.000 abstract 1
- 230000003472 neutralizing effect Effects 0.000 abstract 1
- 229910052759 nickel Inorganic materials 0.000 abstract 1
- 230000000802 nitrating effect Effects 0.000 abstract 1
- QQBPIHBUCMDKFG-GEEYTBSJSA-N phenazopyridine hydrochloride Chemical compound Cl.Nc1ccc(\N=N\c2ccccc2)c(N)n1 QQBPIHBUCMDKFG-GEEYTBSJSA-N 0.000 abstract 1
- OENLEHTYJXMVBG-UHFFFAOYSA-N pyridine;hydrate Chemical compound [OH-].C1=CC=[NH+]C=C1 OENLEHTYJXMVBG-UHFFFAOYSA-N 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 239000000725 suspension Substances 0.000 abstract 1
- 238000010792 warming Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/73—Unsubstituted amino or imino radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
-
- 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
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/34—Fog-inhibitors; Stabilisers; Agents inhibiting latent image regression
-
- 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
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
-
- 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
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/02—Photosensitive materials characterised by the image-forming section
- G03C8/04—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of inorganic or organo-metallic compounds derived from photosensitive noble metals
- G03C8/06—Silver salt diffusion transfer
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US68961167A | 1967-12-11 | 1967-12-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1235747A true GB1235747A (en) | 1971-06-16 |
Family
ID=24769187
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB58958/68A Expired GB1235747A (en) | 1967-12-11 | 1968-12-11 | Antifoggants for photographic products and processes |
Country Status (5)
Country | Link |
---|---|
US (1) | US3473924A (enrdf_load_stackoverflow) |
BE (1) | BE725273A (enrdf_load_stackoverflow) |
FR (1) | FR1594983A (enrdf_load_stackoverflow) |
GB (1) | GB1235747A (enrdf_load_stackoverflow) |
NL (1) | NL159790B (enrdf_load_stackoverflow) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2571924A (en) * | 2018-03-07 | 2019-09-18 | Subsea 7 Ltd | Electrofusion fittings for lined pipes |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3687660A (en) * | 1970-10-15 | 1972-08-29 | Polaroid Corp | Diffusion transfer photographic elements comprising 5-hydroxy-4-azabenzimidazole and a second azabenzimidazole,and processes for their use |
DE2118943C3 (de) * | 1971-04-19 | 1982-04-01 | Polaroid Corp., 02139 Cambridge, Mass. | Photographisches Aufzeichnungsmaterial für das Diffusionsübertragungsverfahren |
JPS549058B1 (enrdf_load_stackoverflow) * | 1971-04-19 | 1979-04-20 | ||
US3833370A (en) * | 1973-01-05 | 1974-09-03 | Polaroid Corp | Color diffusion transfer with development controlling polymeric salt |
US3899331A (en) * | 1973-11-14 | 1975-08-12 | Polaroid Corp | Multicolor dye developer diffusion transfer processes with pyrazolo-{8 3,4d{9 {0 pyrimidines |
US4057425A (en) * | 1975-07-16 | 1977-11-08 | Polaroid Corporation | 2-Substituted benzimidazoles in multicolor diffusion transfer |
US4292391A (en) * | 1980-02-06 | 1981-09-29 | E. I. Du Pont De Nemours And Company | Silver halide development accelerators |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2324123A (en) * | 1941-07-08 | 1943-07-13 | Eastman Kodak Co | Fog inhibitor for photographic developers |
US2353754A (en) * | 1942-11-07 | 1944-07-18 | Eastman Kodak Co | Color photography using metallic salt coupler compounds |
BE559754A (enrdf_load_stackoverflow) * | 1956-08-03 | |||
NL126854C (enrdf_load_stackoverflow) * | 1960-08-22 | |||
NL268156A (enrdf_load_stackoverflow) * | 1960-08-22 | |||
US3212893A (en) * | 1961-03-27 | 1965-10-19 | Eastman Kodak Co | Photographic multicolor diffusion transfer process using dye developers |
US3271154A (en) * | 1961-11-30 | 1966-09-06 | Gen Aniline & Film Corp | Antifogging and stabilizing agents for photography |
US3307947A (en) * | 1964-12-16 | 1967-03-07 | Polaroid Corp | Photographic products and processes |
-
1967
- 1967-12-11 US US689611A patent/US3473924A/en not_active Expired - Lifetime
-
1968
- 1968-12-10 FR FR1594983D patent/FR1594983A/fr not_active Expired
- 1968-12-11 GB GB58958/68A patent/GB1235747A/en not_active Expired
- 1968-12-11 NL NL6817754.A patent/NL159790B/xx not_active IP Right Cessation
- 1968-12-11 BE BE725273D patent/BE725273A/xx not_active IP Right Cessation
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2571924A (en) * | 2018-03-07 | 2019-09-18 | Subsea 7 Ltd | Electrofusion fittings for lined pipes |
GB2571924B (en) * | 2018-03-07 | 2020-10-14 | Subsea 7 Ltd | Electrofusion fittings for lined pipes |
Also Published As
Publication number | Publication date |
---|---|
DE1814020B2 (de) | 1977-03-03 |
US3473924A (en) | 1969-10-21 |
DE1814020A1 (de) | 1969-12-11 |
BE725273A (enrdf_load_stackoverflow) | 1969-06-11 |
NL159790B (nl) | 1979-03-15 |
NL6817754A (enrdf_load_stackoverflow) | 1969-06-13 |
FR1594983A (enrdf_load_stackoverflow) | 1970-06-08 |
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