GB691989A - Photographic non-diffusing color formers - Google Patents
Photographic non-diffusing color formersInfo
- Publication number
- GB691989A GB691989A GB84/51A GB8451A GB691989A GB 691989 A GB691989 A GB 691989A GB 84/51 A GB84/51 A GB 84/51A GB 8451 A GB8451 A GB 8451A GB 691989 A GB691989 A GB 691989A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- prepared
- naphthol
- refluxing
- acetyl
- 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
- 238000010992 reflux Methods 0.000 abstract 9
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 7
- WFDIJRYMOXRFFG-UHFFFAOYSA-N acetic acid anhydride Natural products CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 abstract 7
- 239000002253 acid Substances 0.000 abstract 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 5
- -1 4 - Carboxyphenyl Chemical group 0.000 abstract 4
- KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 abstract 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract 3
- 229960000583 acetic acid Drugs 0.000 abstract 3
- RTGWIFXXIBLLQU-UHFFFAOYSA-N 2-amino-4-methyl-6-(octadecanoylamino)benzenesulfonic acid Chemical compound NC=1C(=C(C=C(C1)C)NC(CCCCCCCCCCCCCCCCC)=O)S(=O)(=O)O RTGWIFXXIBLLQU-UHFFFAOYSA-N 0.000 abstract 2
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 abstract 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N alpha-naphthol Natural products C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 abstract 2
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 abstract 2
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 abstract 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 abstract 2
- 150000003222 pyridines Chemical class 0.000 abstract 2
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 abstract 2
- 239000004296 sodium metabisulphite Substances 0.000 abstract 2
- 235000010262 sodium metabisulphite Nutrition 0.000 abstract 2
- 159000000000 sodium salts Chemical class 0.000 abstract 2
- MUEHADHOTBZWBO-UHFFFAOYSA-N 3-[[3-[acetyl-(5-hydroxynaphthalen-2-yl)amino]benzoyl]amino]-4-(octadecylamino)benzenesulfonic acid Chemical compound C(C)(=O)N(C1=CC(=CC=C1)C(NC1=C(C=CC(=C1)S(=O)(=O)O)NCCCCCCCCCCCCCCCCCC)=O)C=1C=C2C=CC=C(C2=CC=1)O MUEHADHOTBZWBO-UHFFFAOYSA-N 0.000 abstract 1
- XYLPLVUYPAPCML-UHFFFAOYSA-N 5-chloropyridine-3-carboxylic acid Chemical compound OC(=O)C1=CN=CC(Cl)=C1 XYLPLVUYPAPCML-UHFFFAOYSA-N 0.000 abstract 1
- UAMDHIZCOZSZFZ-UHFFFAOYSA-N 6-[acetyl-(5-hydroxynaphthalen-2-yl)amino]-2-methyl-N-octadecylquinoline-4-carboxamide Chemical compound C(C)(=O)N(C=1C=C2C=CC=C(C2=CC1)O)C=1C=C2C(=CC(=NC2=CC1)C)C(NCCCCCCCCCCCCCCCCCC)=O UAMDHIZCOZSZFZ-UHFFFAOYSA-N 0.000 abstract 1
- NZTPZUIIYNYZKT-UHFFFAOYSA-N 6-aminonaphthalene-2-carboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(N)=CC=C21 NZTPZUIIYNYZKT-UHFFFAOYSA-N 0.000 abstract 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 abstract 1
- PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 abstract 1
- 125000003047 N-acetyl group Chemical group 0.000 abstract 1
- OVIFWPXOJVGZFR-UHFFFAOYSA-M NC=1C=C(C=CC1S(=O)(=O)[O-])C.[K+] Chemical compound NC=1C=C(C=CC1S(=O)(=O)[O-])C.[K+] OVIFWPXOJVGZFR-UHFFFAOYSA-M 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- 229960004050 aminobenzoic acid Drugs 0.000 abstract 1
- 239000000908 ammonium hydroxide Substances 0.000 abstract 1
- 238000001914 filtration Methods 0.000 abstract 1
- 239000012362 glacial acetic acid Substances 0.000 abstract 1
- 230000007935 neutral effect Effects 0.000 abstract 1
- 230000000802 nitrating effect Effects 0.000 abstract 1
- WTBAHSZERDXKKZ-UHFFFAOYSA-N octadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCCCC(Cl)=O WTBAHSZERDXKKZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000011591 potassium Substances 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- 235000011056 potassium acetate Nutrition 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 229940037312 stearamide Drugs 0.000 abstract 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 abstract 1
- 239000008096 xylene Substances 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
- G03C7/3244—Couplers forming azinic dyes; Specific developers therefor
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US137886A US2591642A (en) | 1950-01-10 | 1950-01-10 | Nondiffusing color formers comprising aryl j-acids in which the aryl radical is provided with a nondiffusing group |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB691989A true GB691989A (en) | 1953-05-27 |
Family
ID=22479487
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB84/51A Expired GB691989A (en) | 1950-01-10 | 1951-01-01 | Photographic non-diffusing color formers |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US2591642A (enExample) |
| BE (1) | BE500494A (enExample) |
| DE (1) | DE874248C (enExample) |
| GB (1) | GB691989A (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2871120A (en) * | 1955-11-18 | 1959-01-27 | Gen Aniline & Film Corp | Azine cyan color formers |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1273137B (de) * | 1955-04-12 | 1968-07-18 | Arthur J Schmitt Foundation Ch | Verwendung einer UEberzugsmasse als Formsand-Bindemittel |
| US3099559A (en) * | 1959-08-31 | 1963-07-30 | Gen Aniline & Film Corp | Silver-free color reproduction process and composition therefor |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE416898A (enExample) * | 1935-08-07 | |||
| BE488697A (enExample) * | 1948-05-06 |
-
0
- BE BE500494D patent/BE500494A/xx unknown
-
1950
- 1950-01-10 US US137886A patent/US2591642A/en not_active Expired - Lifetime
-
1951
- 1951-01-01 GB GB84/51A patent/GB691989A/en not_active Expired
- 1951-01-10 DE DEG4984A patent/DE874248C/de not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2871120A (en) * | 1955-11-18 | 1959-01-27 | Gen Aniline & Film Corp | Azine cyan color formers |
Also Published As
| Publication number | Publication date |
|---|---|
| DE874248C (de) | 1953-04-23 |
| BE500494A (enExample) | |
| US2591642A (en) | 1952-04-01 |
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