GB1153561A - Improvements relating to the Producion of Colour Images - Google Patents
Improvements relating to the Producion of Colour ImagesInfo
- Publication number
- GB1153561A GB1153561A GB2241/66A GB224166A GB1153561A GB 1153561 A GB1153561 A GB 1153561A GB 2241/66 A GB2241/66 A GB 2241/66A GB 224166 A GB224166 A GB 224166A GB 1153561 A GB1153561 A GB 1153561A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bromo
- chloro
- amino
- methoxynitrobenzene
- hexadecyl
- 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
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 238000010438 heat treatment Methods 0.000 abstract 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 3
- MEQKSFQEPDRNEQ-UHFFFAOYSA-N 1-bromo-3-methoxy-5-nitrobenzene Chemical compound COC1=CC(Br)=CC([N+]([O-])=O)=C1 MEQKSFQEPDRNEQ-UHFFFAOYSA-N 0.000 abstract 2
- IYHHGLULQDOFGC-UHFFFAOYSA-N 1-chloro-3-methyl-5-nitrobenzene Chemical compound CC1=CC(Cl)=CC([N+]([O-])=O)=C1 IYHHGLULQDOFGC-UHFFFAOYSA-N 0.000 abstract 2
- QYLWEPIKPMUYAW-UHFFFAOYSA-N 2-bromo-6-methoxy-4-nitroaniline Chemical compound COC1=CC([N+]([O-])=O)=CC(Br)=C1N QYLWEPIKPMUYAW-UHFFFAOYSA-N 0.000 abstract 2
- FHUSNGUPJXGLPL-UHFFFAOYSA-N 3-bromo-5-methoxyaniline Chemical compound COC1=CC(N)=CC(Br)=C1 FHUSNGUPJXGLPL-UHFFFAOYSA-N 0.000 abstract 2
- XUZCJDBXXYJXDD-UHFFFAOYSA-N 3-chloro-5-methylaniline Chemical compound CC1=CC(N)=CC(Cl)=C1 XUZCJDBXXYJXDD-UHFFFAOYSA-N 0.000 abstract 2
- 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 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 abstract 2
- 125000001246 bromo group Chemical group Br* 0.000 abstract 2
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 2
- 235000019253 formic acid Nutrition 0.000 abstract 2
- 150000002431 hydrogen Chemical class 0.000 abstract 2
- -1 γ-sulphopropyl Chemical group 0.000 abstract 2
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 abstract 1
- MYMSJFSOOQERIO-UHFFFAOYSA-N 1-bromodecane Chemical compound CCCCCCCCCCBr MYMSJFSOOQERIO-UHFFFAOYSA-N 0.000 abstract 1
- HNTGIJLWHDPAFN-UHFFFAOYSA-N 1-bromohexadecane Chemical compound CCCCCCCCCCCCCCCCBr HNTGIJLWHDPAFN-UHFFFAOYSA-N 0.000 abstract 1
- UGXUJYWOKLTNET-UHFFFAOYSA-N 2-chloro-4-methyl-6-nitroaniline Chemical compound CC1=CC(Cl)=C(N)C([N+]([O-])=O)=C1 UGXUJYWOKLTNET-UHFFFAOYSA-N 0.000 abstract 1
- GVBHRNIWBGTNQA-UHFFFAOYSA-N 2-methoxy-4-nitroaniline Chemical compound COC1=CC([N+]([O-])=O)=CC=C1N GVBHRNIWBGTNQA-UHFFFAOYSA-N 0.000 abstract 1
- YIZRPAWCIFTHNA-UHFFFAOYSA-N 3-bromo-5-methylaniline Chemical compound CC1=CC(N)=CC(Br)=C1 YIZRPAWCIFTHNA-UHFFFAOYSA-N 0.000 abstract 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 abstract 1
- KTHQWIFNBZERPZ-UHFFFAOYSA-N N-[(2,4,5-trimethylphenyl)methyl]nitramide Chemical compound [N+](=O)([O-])NCC=1C(C)=CC(C)=C(C)C1 KTHQWIFNBZERPZ-UHFFFAOYSA-N 0.000 abstract 1
- SWKLMYUDTHRKGN-UHFFFAOYSA-N N-[(decylamino)-(2,4,5-trimethylphenyl)methyl]formamide Chemical compound C(CCCCCCCCC)NC(C=1C(C)=CC(C)=C(C)C1)NC=O SWKLMYUDTHRKGN-UHFFFAOYSA-N 0.000 abstract 1
- ONRZTVAADPBAMG-UHFFFAOYSA-N N-[amino-(2,4,5-trimethylphenyl)methyl]formamide Chemical compound NC(C=1C(C)=CC(C)=C(C)C1)NC=O ONRZTVAADPBAMG-UHFFFAOYSA-N 0.000 abstract 1
- XFZOXYYIHFLFCZ-UHFFFAOYSA-N N-[nitro-(2,4,5-trimethylphenyl)methyl]formamide Chemical compound [N+](=O)([O-])C(C=1C(C)=CC(C)=C(C)C1)NC=O XFZOXYYIHFLFCZ-UHFFFAOYSA-N 0.000 abstract 1
- OJGMBLNIHDZDGS-UHFFFAOYSA-N N-ethyl-N-phenylamine Natural products CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 abstract 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 abstract 1
- 229940045803 cuprous chloride Drugs 0.000 abstract 1
- 150000001989 diazonium salts Chemical class 0.000 abstract 1
- 238000001704 evaporation Methods 0.000 abstract 1
- 150000003840 hydrochlorides Chemical class 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 abstract 1
- 150000004989 p-phenylenediamines Chemical class 0.000 abstract 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 abstract 1
- 238000010992 reflux Methods 0.000 abstract 1
- 235000011150 stannous chloride Nutrition 0.000 abstract 1
- 239000001119 stannous chloride 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
- G03C7/18—Processes for the correction of the colour image in subtractive colour photography
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2241/66A GB1153561A (en) | 1966-01-18 | 1966-01-18 | Improvements relating to the Producion of Colour Images |
| BE692636D BE692636A (sv) | 1966-01-18 | 1967-01-16 | |
| FR91845A FR1508682A (fr) | 1966-01-18 | 1967-01-17 | Procédé de formation d'images photographiques en couleurs |
| NL6700716A NL6700716A (sv) | 1966-01-18 | 1967-01-17 | |
| US610023A US3535113A (en) | 1966-01-18 | 1967-01-18 | Production of color masking images using p-phenylenediamine mask-forming compounds |
| DE19671644046 DE1644046A1 (de) | 1966-01-18 | 1967-01-18 | Verfahren zur Herstellung photographischer Farbbilder |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2241/66A GB1153561A (en) | 1966-01-18 | 1966-01-18 | Improvements relating to the Producion of Colour Images |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1153561A true GB1153561A (en) | 1969-05-29 |
Family
ID=9736087
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2241/66A Expired GB1153561A (en) | 1966-01-18 | 1966-01-18 | Improvements relating to the Producion of Colour Images |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3535113A (sv) |
| BE (1) | BE692636A (sv) |
| DE (1) | DE1644046A1 (sv) |
| FR (1) | FR1508682A (sv) |
| GB (1) | GB1153561A (sv) |
| NL (1) | NL6700716A (sv) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE786710A (fr) * | 1971-10-04 | 1973-01-25 | Bristol Myers Co | Composition pour la teinture du cheveu avec |
| US4066456A (en) * | 1974-12-10 | 1978-01-03 | Gaf Corporation | Incorporated carboxy substituted p-phenylenediamine color developer |
| US4066457A (en) * | 1974-12-10 | 1978-01-03 | Gaf Corporation | Color developer for diffusion transfer |
| JPS60164499A (ja) * | 1984-02-07 | 1985-08-27 | Kyowa Medetsukusu Kk | 酵素活性測定法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE519872A (sv) * | 1952-05-13 | |||
| BE567154A (sv) * | 1957-04-26 |
-
1966
- 1966-01-18 GB GB2241/66A patent/GB1153561A/en not_active Expired
-
1967
- 1967-01-16 BE BE692636D patent/BE692636A/xx unknown
- 1967-01-17 NL NL6700716A patent/NL6700716A/xx unknown
- 1967-01-17 FR FR91845A patent/FR1508682A/fr not_active Expired
- 1967-01-18 US US610023A patent/US3535113A/en not_active Expired - Lifetime
- 1967-01-18 DE DE19671644046 patent/DE1644046A1/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| US3535113A (en) | 1970-10-20 |
| FR1508682A (fr) | 1968-01-05 |
| NL6700716A (sv) | 1967-03-28 |
| BE692636A (sv) | 1967-07-17 |
| DE1644046A1 (de) | 1971-04-15 |
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