GB1105962A - Colour photographic materials and processes - Google Patents
Colour photographic materials and processesInfo
- Publication number
- GB1105962A GB1105962A GB2679464A GB2679464A GB1105962A GB 1105962 A GB1105962 A GB 1105962A GB 2679464 A GB2679464 A GB 2679464A GB 2679464 A GB2679464 A GB 2679464A GB 1105962 A GB1105962 A GB 1105962A
- Authority
- GB
- United Kingdom
- Prior art keywords
- pyrazolone
- nitrophenyl
- reacting
- nitro
- 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
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 6
- -1 4 - n - dodecylphenyl Chemical group 0.000 abstract 4
- GMOVHLZDVIVTAW-UHFFFAOYSA-N 5-amino-2-(4-nitrophenyl)-4h-pyrazol-3-one Chemical compound O=C1CC(N)=NN1C1=CC=C([N+]([O-])=O)C=C1 GMOVHLZDVIVTAW-UHFFFAOYSA-N 0.000 abstract 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 4
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 abstract 3
- ZSZUZHXUJXYSMM-UHFFFAOYSA-N ethyl 3-oxoicosanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)CC(=O)OCC ZSZUZHXUJXYSMM-UHFFFAOYSA-N 0.000 abstract 2
- 150000007857 hydrazones Chemical class 0.000 abstract 2
- HORQAOAYAYGIBM-UHFFFAOYSA-N 2,4-dinitrophenylhydrazine Chemical compound NNC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O HORQAOAYAYGIBM-UHFFFAOYSA-N 0.000 abstract 1
- BXWAGNNCASBCKI-UHFFFAOYSA-N 2-(2,4-dinitrophenyl)-5-heptadecyl-4h-pyrazol-3-one Chemical compound O=C1CC(CCCCCCCCCCCCCCCCC)=NN1C1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O BXWAGNNCASBCKI-UHFFFAOYSA-N 0.000 abstract 1
- VEHDWLHOEXDHFQ-UHFFFAOYSA-N 4-(3-heptadecyl-5-oxo-4H-pyrazol-1-yl)-3-nitrobenzenesulfonic acid Chemical compound [N+](=O)([O-])C1=C(C=CC(=C1)S(=O)(=O)O)N1N=C(CC1=O)CCCCCCCCCCCCCCCCC VEHDWLHOEXDHFQ-UHFFFAOYSA-N 0.000 abstract 1
- JVNUKJQMJYKJCW-UHFFFAOYSA-N 4-[3-heptadecyl-4-[(4-methoxyphenyl)diazenyl]-5-oxo-4H-pyrazol-1-yl]-3-nitrobenzenesulfonic acid Chemical compound [N+](=O)([O-])C1=C(C=CC(=C1)S(=O)(=O)O)N1N=C(C(C1=O)N=NC1=CC=C(C=C1)OC)CCCCCCCCCCCCCCCCC JVNUKJQMJYKJCW-UHFFFAOYSA-N 0.000 abstract 1
- KLPPPIIIEMUEGP-UHFFFAOYSA-N 4-dodecylaniline Chemical compound CCCCCCCCCCCCC1=CC=C(N)C=C1 KLPPPIIIEMUEGP-UHFFFAOYSA-N 0.000 abstract 1
- DZRLKMNAQIOEOG-UHFFFAOYSA-N 4-hydrazinyl-3-nitrobenzenesulfonic acid Chemical compound NNC1=CC=C(S(O)(=O)=O)C=C1[N+]([O-])=O DZRLKMNAQIOEOG-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
- JYKYELVBACQBCY-UHFFFAOYSA-N 5-(4-dodecylphenyl)imino-2-(4-nitrophenyl)pyrazolidin-3-one Chemical compound [N+](=O)([O-])C1=CC=C(C=C1)N1N=C(CC1=O)NC1=CC=C(C=C1)CCCCCCCCCCCC JYKYELVBACQBCY-UHFFFAOYSA-N 0.000 abstract 1
- AFKHIUMDWUPZTP-UHFFFAOYSA-N N-(4-dodecylphenyl)-1,3-dioxo-2-benzofuran-5-carboxamide Chemical compound C(CCCCCCCCCCC)C1=CC=C(C=C1)NC(=O)C=1C=C2C(C(=O)OC2=O)=CC1 AFKHIUMDWUPZTP-UHFFFAOYSA-N 0.000 abstract 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 abstract 1
- UGQZLDXDWSPAOM-UHFFFAOYSA-N pyrrolo[3,4-f]isoindole-1,3,5,7-tetrone Chemical compound C1=C2C(=O)NC(=O)C2=CC2=C1C(=O)NC2=O UGQZLDXDWSPAOM-UHFFFAOYSA-N 0.000 abstract 1
- 159000000000 sodium salts Chemical class 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D231/44—Oxygen and nitrogen or sulfur and nitrogen atoms
- C07D231/52—Oxygen atom in position 3 and nitrogen atom in position 5, or vice versa
-
- 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
- G03C7/18—Processes for the correction of the colour image in subtractive colour photography
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Coloring (AREA)
Abstract
N - (4 - n - dodecylphenyl) - N1 - (1 - [4 - nitrophenyl - 5 - pyrazolonyl - 3) pyromellitic diimide is obtained by reacting 1-(4-nitro-phenyl)-3 - amino - 5 - pyrazolone with N - (4 - n - dodecylphenyl) pyromellitic monoimide monoanhydride. 1 - (4 - nitrophenyl) - 3 - (a - sulphostearoylamino) - 5 - pyrazolone is obtained by reacting 1 - (4 - nitrophenyl) - 3 - amino - 5 - pyrazolone with a -sulphostearic acid monosodium salt. 4-(4n-Dodecylphenylaminocarbonyl) - N - [1 - (4 - nitrophenyl) - 5 - pyrazolonyl-3] phthalimide is obtained by reacting 4-(4-n-dodecylphenylaminocarbonyl) phthalic anhydride with 1-(4-nitrophenyl)-3-amino-5-pyrazolone. 1 - (4 - nitrophenyl) - 3 - (4 - n - dodecylanilino)-5-pyrazolone is obtained by reacting 1 - (4 - nitrophenyl) - 3 - amino - 5 - pyrazolone with 4-n-dodecylaniline in acetic acid. The sodium salt of the corresponding 3-sulpho anilino compound is prepared by reaction of the product with conc. sulphuric acid in the presence of Na+. 1-(2,4-dinitrophenyl) - 3 - heptadecyl - 5 - pyrazolone is obtained by reacting ethylstearoylacetate with 2,4-dinitrophenylhydrazine in acetic acid to give the corresponding hydrazone, followed by treatment with NaOH/ethanol. 1 - (2 - nitro - 4 - sulphophenyl) - 3 - heptadecyl - 4 - (4 - methoxy - phenylazo)-5-pyrazolone is obtained by reacting ethylstearoylacetate with 2-nitro-4-sulphophenyl hydrazine to give the corresponding hydrazone which is cyclized by treatment with NaOH/ethanol to 1-(2-nitro-4-sulphophenyl)-3-heptadecyl-5-pyrazolone, which compound is reacted with 4-methoxybenzene diazonium chloride to form the azo compound.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2679464A GB1105962A (en) | 1964-06-29 | 1964-06-29 | Colour photographic materials and processes |
| FR22684A FR1438036A (en) | 1964-06-29 | 1965-06-29 | Improvements in color photography |
| NL6508337A NL6508337A (en) | 1964-06-29 | 1965-06-29 | |
| BE666091A BE666091A (en) | 1964-06-29 | 1965-06-29 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2679464A GB1105962A (en) | 1964-06-29 | 1964-06-29 | Colour photographic materials and processes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1105962A true GB1105962A (en) | 1968-03-13 |
Family
ID=10249325
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2679464A Expired GB1105962A (en) | 1964-06-29 | 1964-06-29 | Colour photographic materials and processes |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE666091A (en) |
| GB (1) | GB1105962A (en) |
| NL (1) | NL6508337A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7329039B2 (en) | 1998-10-28 | 2008-02-12 | Covaris, Inc. | Systems and methods for determining a state of fluidization and/or a state of mixing |
| US7687039B2 (en) | 1998-10-28 | 2010-03-30 | Covaris, Inc. | Methods and systems for modulating acoustic energy delivery |
| US7757561B2 (en) | 2005-08-01 | 2010-07-20 | Covaris, Inc. | Methods and systems for processing samples using acoustic energy |
| US8353619B2 (en) | 2006-08-01 | 2013-01-15 | Covaris, Inc. | Methods and apparatus for treating samples with acoustic energy |
-
1964
- 1964-06-29 GB GB2679464A patent/GB1105962A/en not_active Expired
-
1965
- 1965-06-29 NL NL6508337A patent/NL6508337A/xx unknown
- 1965-06-29 BE BE666091A patent/BE666091A/xx unknown
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7329039B2 (en) | 1998-10-28 | 2008-02-12 | Covaris, Inc. | Systems and methods for determining a state of fluidization and/or a state of mixing |
| US7521023B2 (en) | 1998-10-28 | 2009-04-21 | Covaris, Inc. | Apparatus and methods for controlling sonic treatment |
| US7687039B2 (en) | 1998-10-28 | 2010-03-30 | Covaris, Inc. | Methods and systems for modulating acoustic energy delivery |
| US7757561B2 (en) | 2005-08-01 | 2010-07-20 | Covaris, Inc. | Methods and systems for processing samples using acoustic energy |
| US8353619B2 (en) | 2006-08-01 | 2013-01-15 | Covaris, Inc. | Methods and apparatus for treating samples with acoustic energy |
Also Published As
| Publication number | Publication date |
|---|---|
| BE666091A (en) | 1965-10-18 |
| NL6508337A (en) | 1965-12-30 |
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