GB347430A - - Google Patents
Info
- Publication number
- GB347430A GB347430A GB10012/30A GB1001230A GB347430A GB 347430 A GB347430 A GB 347430A GB 10012/30 A GB10012/30 A GB 10012/30A GB 1001230 A GB1001230 A GB 1001230A GB 347430 A GB347430 A GB 347430A
- Authority
- GB
- United Kingdom
- Prior art keywords
- thiourea
- boric
- layers
- amino
- biguanidine
- 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
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 abstract 10
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 abstract 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 5
- 235000002906 tartaric acid Nutrition 0.000 abstract 5
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 abstract 4
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- 239000011975 tartaric acid Substances 0.000 abstract 3
- PQMFVUNERGGBPG-UHFFFAOYSA-N (6-bromopyridin-2-yl)hydrazine Chemical compound NNC1=CC=CC(Br)=N1 PQMFVUNERGGBPG-UHFFFAOYSA-N 0.000 abstract 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 abstract 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 2
- 239000004327 boric acid Substances 0.000 abstract 2
- 235000010338 boric acid Nutrition 0.000 abstract 2
- 150000008049 diazo compounds Chemical class 0.000 abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 2
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 abstract 2
- 229960001553 phloroglucinol Drugs 0.000 abstract 2
- 239000011592 zinc chloride Substances 0.000 abstract 2
- 235000005074 zinc chloride Nutrition 0.000 abstract 2
- GWEHVDNNLFDJLR-UHFFFAOYSA-N 1,3-diphenylurea Chemical compound C=1C=CC=CC=1NC(=O)NC1=CC=CC=C1 GWEHVDNNLFDJLR-UHFFFAOYSA-N 0.000 abstract 1
- ZYSOYLBBCYWEMB-UHFFFAOYSA-N 7-aminonaphthalen-1-ol Chemical compound C1=CC=C(O)C2=CC(N)=CC=C21 ZYSOYLBBCYWEMB-UHFFFAOYSA-N 0.000 abstract 1
- HCHRPHAOXFUFJH-UHFFFAOYSA-N NC(=N)NNC(=N)N.OC1=CC=CC2=CC=CC=C12 Chemical compound NC(=N)NNC(=N)N.OC1=CC=CC2=CC=CC=C12 HCHRPHAOXFUFJH-UHFFFAOYSA-N 0.000 abstract 1
- GVTKFZHQGDNNFU-UHFFFAOYSA-N S(=O)(=O)(O)OS(=O)(=O)OS(=O)(=O)O.C1=CC=CC2=CC=CC=C12 Chemical compound S(=O)(=O)(O)OS(=O)(=O)OS(=O)(=O)O.C1=CC=CC2=CC=CC=C12 GVTKFZHQGDNNFU-UHFFFAOYSA-N 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 239000001164 aluminium sulphate Substances 0.000 abstract 1
- 235000011128 aluminium sulphate Nutrition 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 abstract 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 abstract 1
- 239000001166 ammonium sulphate Substances 0.000 abstract 1
- 235000011130 ammonium sulphate Nutrition 0.000 abstract 1
- 229950011260 betanaphthol Drugs 0.000 abstract 1
- 229910021538 borax Inorganic materials 0.000 abstract 1
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 abstract 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 abstract 1
- AXJDDGOHBYMCAJ-UHFFFAOYSA-N n-(3,4-dimethoxyphenyl)benzamide Chemical compound C1=C(OC)C(OC)=CC=C1NC(=O)C1=CC=CC=C1 AXJDDGOHBYMCAJ-UHFFFAOYSA-N 0.000 abstract 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 1
- 229910000029 sodium carbonate Inorganic materials 0.000 abstract 1
- 239000004328 sodium tetraborate Substances 0.000 abstract 1
- 235000010339 sodium tetraborate Nutrition 0.000 abstract 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 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
- G03C1/00—Photosensitive materials
- G03C1/52—Compositions containing diazo compounds as photosensitive substances
- G03C1/54—Diazonium salts or diazo anhydrides
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
347,430. Photographic diazotype layers. KALLE & CO. AKT.-GES., 23, Rheinstrasse, Biebrich-on-Rhine, Wiesbaden, Germany. March 28, 1930, No. 10012. Convention date, March 30, 1929. [Class 98 (ii).] Diazo compounds of aromatic amino compounds substituted by acylamino or thioacylamino group are used in the preparation of light sensitive layers. Tetrazo groups containing two amino groups in the acyl residue may be used. Examples are given of layers containing (1) the tin chloride double salt of tetrazo-diaminodiphenyl-thiourea, boric and tartaric acid and thiourea, (2) tetrazo-diaminotetramethoxy diphenylurea, tartaric acid and thiourea, both layers being developed with phloroglucinol and borax, (3) the zinc chloride double salt of 1-amino-2: 5-diethoxy-4-benzoylamino benzene, 1-hydroxy naphthalene-7-biguanidine, naphthalene trisulphuric acid, boric and tartaric acids, thiourea and ammonium sulphate developed with ammonia or sodium carbonate, (4) the diazo compound referred to under (3) above, boric and tartaric acid and thiourea developed with phloroglucinol, 1: 7-aminonaphthol, 2: 7-dihydroxynaphthalene or 1: 7 hydroxynaphthalene-biguanidine, (5) the zinc chloride double salt of diazo 1-amino-2: 5 dimethoxy-4-benzoylamino benzene, aluminium sulphate, boric and tartaric acids and thiourea, suitable developers being beta-naphthol, resorcine, 1-hydroxynaphthalene-1-biguanidine and 1-hydroxy naphthalene-7-phenyl guanidine.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEK0114139 | 1929-03-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB347430A true GB347430A (en) | 1931-04-30 |
Family
ID=7242946
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB10012/30A Expired GB347430A (en) | 1929-03-30 | 1930-03-28 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US1816989A (en) |
| BE (1) | BE369000A (en) |
| ES (1) | ES117245A1 (en) |
| FR (1) | FR693032A (en) |
| GB (1) | GB347430A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL61567C (en) * | 1945-09-07 | |||
| BE471525A (en) * | 1946-03-20 | |||
| US2657141A (en) * | 1947-07-14 | 1953-10-27 | Grinten Chem L V D | Diazotype developer composition containing a potassium borate and process of using same |
| US2537919A (en) * | 1948-05-05 | 1951-01-09 | Gen Aniline & Film Corp | Diazotype layer containing three coupling components for neutral black shades |
-
0
- BE BE369000D patent/BE369000A/xx unknown
-
1930
- 1930-03-12 ES ES0117245A patent/ES117245A1/en not_active Expired
- 1930-03-24 US US438648A patent/US1816989A/en not_active Expired - Lifetime
- 1930-03-28 GB GB10012/30A patent/GB347430A/en not_active Expired
- 1930-03-29 FR FR693032D patent/FR693032A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BE369000A (en) | |
| US1816989A (en) | 1931-08-04 |
| ES117245A1 (en) | 1930-04-16 |
| FR693032A (en) | 1930-11-14 |
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