DE1051635B - Verfahren zur Erzeugung eines gelben Farbstoffbildes mit Hilfe von Azofarbstoffen nach dem Silberfarbbleichverfahren in einer photographischen Schicht, insbesondere fuerfarbenphotographische Zwecke - Google Patents
Verfahren zur Erzeugung eines gelben Farbstoffbildes mit Hilfe von Azofarbstoffen nach dem Silberfarbbleichverfahren in einer photographischen Schicht, insbesondere fuerfarbenphotographische ZweckeInfo
- Publication number
- DE1051635B DE1051635B DEG24496A DEG0024496A DE1051635B DE 1051635 B DE1051635 B DE 1051635B DE G24496 A DEG24496 A DE G24496A DE G0024496 A DEG0024496 A DE G0024496A DE 1051635 B DE1051635 B DE 1051635B
- Authority
- DE
- Germany
- Prior art keywords
- yellow
- dye
- amino
- silver
- layer
- 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.)
- Pending
Links
- 239000000975 dye Substances 0.000 title claims description 58
- 229910052709 silver Inorganic materials 0.000 title claims description 30
- 239000004332 silver Substances 0.000 title claims description 30
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 title claims description 25
- 238000000034 method Methods 0.000 title claims description 19
- 238000004061 bleaching Methods 0.000 title claims description 12
- 239000001043 yellow dye Substances 0.000 title claims description 11
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 title claims description 8
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 239000000987 azo dye Substances 0.000 title claims description 3
- 235000005979 Citrus limon Nutrition 0.000 claims description 18
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 18
- -1 silver halide Chemical class 0.000 claims description 18
- 229920000159 gelatin Polymers 0.000 claims description 16
- 239000000839 emulsion Substances 0.000 claims description 15
- 235000019322 gelatine Nutrition 0.000 claims description 15
- 239000008273 gelatin Substances 0.000 claims description 12
- 108010010803 Gelatin Proteins 0.000 claims description 11
- 235000011852 gelatine desserts Nutrition 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 239000011780 sodium chloride Substances 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 8
- 230000008878 coupling Effects 0.000 claims description 8
- 238000010168 coupling process Methods 0.000 claims description 8
- 238000005859 coupling reaction Methods 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 7
- 239000007844 bleaching agent Substances 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 239000001828 Gelatine Substances 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 4
- 244000248349 Citrus limon Species 0.000 claims description 3
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 claims 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims 2
- FKHNZQFCDGOQGV-UHFFFAOYSA-N 2,3-dimethylquinoxaline Chemical compound C1=CC=C2N=C(C)C(C)=NC2=C1 FKHNZQFCDGOQGV-UHFFFAOYSA-N 0.000 claims 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 claims 1
- 239000004133 Sodium thiosulphate Substances 0.000 claims 1
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims 1
- 239000013078 crystal Substances 0.000 claims 1
- 230000005484 gravity Effects 0.000 claims 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 claims 1
- 235000019345 sodium thiosulphate Nutrition 0.000 claims 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 claims 1
- 244000131522 Citrus pyriformis Species 0.000 description 15
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 14
- 239000002253 acid Substances 0.000 description 13
- 239000000243 solution Substances 0.000 description 12
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000000843 powder Substances 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 5
- 230000007935 neutral effect Effects 0.000 description 5
- JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- ZLYYJUJDFKGVKB-OWOJBTEDSA-N (e)-but-2-enedioyl dichloride Chemical compound ClC(=O)\C=C\C(Cl)=O ZLYYJUJDFKGVKB-OWOJBTEDSA-N 0.000 description 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 3
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- ZQHJVIHCDHJVII-UPHRSURJSA-N (z)-2-chlorobut-2-enedioic acid Chemical compound OC(=O)\C=C(/Cl)C(O)=O ZQHJVIHCDHJVII-UPHRSURJSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 2
- KBOPZPXVLCULAV-UHFFFAOYSA-N mesalamine Chemical compound NC1=CC=C(O)C(C(O)=O)=C1 KBOPZPXVLCULAV-UHFFFAOYSA-N 0.000 description 2
- WXWCDTXEKCVRRO-UHFFFAOYSA-N para-Cresidine Chemical compound COC1=CC=C(C)C=C1N WXWCDTXEKCVRRO-UHFFFAOYSA-N 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 150000003378 silver Chemical class 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- LATZCKQPCAXJJJ-NSCUHMNNSA-N (e)-2-methylbut-2-enedioyl dichloride Chemical compound ClC(=O)C(/C)=C/C(Cl)=O LATZCKQPCAXJJJ-NSCUHMNNSA-N 0.000 description 1
- LATZCKQPCAXJJJ-IHWYPQMZSA-N (z)-2-methylbut-2-enedioyl dichloride Chemical compound ClC(=O)C(/C)=C\C(Cl)=O LATZCKQPCAXJJJ-IHWYPQMZSA-N 0.000 description 1
- ZLYYJUJDFKGVKB-UPHRSURJSA-N (z)-but-2-enedioyl dichloride Chemical compound ClC(=O)\C=C/C(Cl)=O ZLYYJUJDFKGVKB-UPHRSURJSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- CHLICZRVGGXEOD-UHFFFAOYSA-N 1-Methoxy-4-methylbenzene Chemical compound COC1=CC=C(C)C=C1 CHLICZRVGGXEOD-UHFFFAOYSA-N 0.000 description 1
- JLUIOEOHOOLSJC-UHFFFAOYSA-N 1H-Pyrrole-2,5-dicarboxylic acid Natural products OC(=O)C1=CC=C(C(O)=O)N1 JLUIOEOHOOLSJC-UHFFFAOYSA-N 0.000 description 1
- CFCXQQUQLZIZPI-UHFFFAOYSA-N 2-amino-3,5-dimethylbenzenesulfonic acid Chemical compound CC1=CC(C)=C(N)C(S(O)(=O)=O)=C1 CFCXQQUQLZIZPI-UHFFFAOYSA-N 0.000 description 1
- KTFUNVBAGAPLLC-UHFFFAOYSA-N 2-amino-5-ethoxybenzenesulfonic acid Chemical compound CCOC1=CC=C(N)C(S(O)(=O)=O)=C1 KTFUNVBAGAPLLC-UHFFFAOYSA-N 0.000 description 1
- LTPSRQRIPCVMKQ-UHFFFAOYSA-N 2-amino-5-methylbenzenesulfonic acid Chemical compound CC1=CC=C(N)C(S(O)(=O)=O)=C1 LTPSRQRIPCVMKQ-UHFFFAOYSA-N 0.000 description 1
- FLIOATBXVNLPLK-UHFFFAOYSA-N 3-amino-4-methoxybenzenesulfonic acid Chemical compound COC1=CC=C(S(O)(=O)=O)C=C1N FLIOATBXVNLPLK-UHFFFAOYSA-N 0.000 description 1
- ZAJAQTYSTDTMCU-UHFFFAOYSA-N 3-aminobenzenesulfonic acid Chemical compound NC1=CC=CC(S(O)(=O)=O)=C1 ZAJAQTYSTDTMCU-UHFFFAOYSA-N 0.000 description 1
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 1
- QTOZDUVONNAWKW-UHFFFAOYSA-N Br/C(/C(=O)Cl)=CC(=O)Cl Chemical compound Br/C(/C(=O)Cl)=CC(=O)Cl QTOZDUVONNAWKW-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- WJJMNDUMQPNECX-UHFFFAOYSA-N Dipicolinic acid Natural products OC(=O)C1=CC=CC(C(O)=O)=N1 WJJMNDUMQPNECX-UHFFFAOYSA-N 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 1
- 125000004442 acylamino group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QFFVPLLCYGOFPU-UHFFFAOYSA-N barium chromate Chemical compound [Ba+2].[O-][Cr]([O-])(=O)=O QFFVPLLCYGOFPU-UHFFFAOYSA-N 0.000 description 1
- FDQSRULYDNDXQB-UHFFFAOYSA-N benzene-1,3-dicarbonyl chloride Chemical compound ClC(=O)C1=CC=CC(C(Cl)=O)=C1 FDQSRULYDNDXQB-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- CHTHALBTIRVDBM-UHFFFAOYSA-N dehydromucic acid Natural products OC(=O)C1=CC=C(C(O)=O)O1 CHTHALBTIRVDBM-UHFFFAOYSA-N 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- NCBZRJODKRCREW-UHFFFAOYSA-N m-anisidine Chemical compound COC1=CC=CC(N)=C1 NCBZRJODKRCREW-UHFFFAOYSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- BLJHLOLVEXWHFS-UHFFFAOYSA-N methyl 2,3-diaminobenzoate Chemical compound COC(=O)C1=CC=CC(N)=C1N BLJHLOLVEXWHFS-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- RBQWGHBZCHFUQU-UHFFFAOYSA-N n-(3-amino-4-methylphenyl)acetamide Chemical compound CC(=O)NC1=CC=C(C)C(N)=C1 RBQWGHBZCHFUQU-UHFFFAOYSA-N 0.000 description 1
- VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- RWEWEOKGGLQXPR-UHFFFAOYSA-N pyridine-2,5-dicarbonyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)N=C1 RWEWEOKGGLQXPR-UHFFFAOYSA-N 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229950000244 sulfanilic acid Drugs 0.000 description 1
- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 description 1
- TXXHDPDFNKHHGW-ZPUQHVIOSA-N trans,trans-muconic acid Chemical compound OC(=O)\C=C\C=C\C(O)=O TXXHDPDFNKHHGW-ZPUQHVIOSA-N 0.000 description 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
- G03C7/28—Silver dye bleach processes; Materials therefor; Preparing or processing such materials
- G03C7/29—Azo dyes therefor
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Plural Heterocyclic Compounds (AREA)
- Paper (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB14809/57A GB841300A (en) | 1957-05-09 | 1957-05-09 | Improvements in or relating to colour photography |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1051635B true DE1051635B (de) | 1959-02-26 |
Family
ID=10047857
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEG24496A Pending DE1051635B (de) | 1957-05-09 | 1958-05-08 | Verfahren zur Erzeugung eines gelben Farbstoffbildes mit Hilfe von Azofarbstoffen nach dem Silberfarbbleichverfahren in einer photographischen Schicht, insbesondere fuerfarbenphotographische Zwecke |
Country Status (7)
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1165998B (de) * | 1961-09-27 | 1964-03-19 | Ciba Geigy | Photographische Schichten fuer das Silberfarbbleichverfahren |
| DE1167651B (de) * | 1961-01-26 | 1964-04-09 | Ciba Geigy | Photographische Schicht fuer das Silberfarbbleichverfahren |
| DE1285880B (de) * | 1962-12-11 | 1968-12-19 | Ciba Geigy | Photographische Materialien fuer das Silberfarbbleichverfahren |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL270722A (US06368395-20020409-C00050.png) * | 1960-10-27 | |||
| NL284975A (US06368395-20020409-C00050.png) * | 1961-11-02 | |||
| CH440967A (de) * | 1964-11-09 | 1967-07-31 | Ciba Geigy | Photographisches Material für das Silberfarbbleichverfahren |
| CH449423A (de) * | 1965-02-22 | 1967-12-31 | Ciba Geigy | Photographisches Material für das Silberfarbbleichverfahren |
| US3498787A (en) * | 1965-08-20 | 1970-03-03 | Eastman Kodak Co | Rapid dye-bleach photographic process and element comprising dye-developers |
| US3538075A (en) * | 1966-12-03 | 1970-11-03 | Basf Ag | Disazo dyes from bis-p,p'-diamino-alkylenedicarboxylic acid anilides |
| TW200815533A (en) * | 2006-05-30 | 2008-04-01 | Mitsubishi Chem Corp | Azo pigment for anisotropic pigment film |
| DE602007003933D1 (de) * | 2006-08-26 | 2010-02-04 | Fujifilm Imaging Colorants Ltd | Tintenstrahldruckverfahren, tinte und färbemittel |
| JP6680211B2 (ja) * | 2014-10-17 | 2020-04-15 | 住友化学株式会社 | 化合物および組成物 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB496559A (en) * | 1936-05-30 | 1938-11-30 | Bela Gaspar | Process for the manufacture of coloured photographic materials |
| GB520529A (en) * | 1938-08-06 | 1940-04-26 | Bela Gaspar | Process for producing colour photographs |
| DE740708C (de) * | 1940-05-07 | 1943-10-27 | Kodak Ag | Verfahren zur Erzeugung von lichtempfindlichen Schichten fuer das Silberblechverfahren |
| US2514234A (en) * | 1939-08-09 | 1950-07-04 | Chromogen Inc | Process for the manufacture of color photographic images |
| GB705171A (en) * | 1950-01-06 | 1954-03-10 | Bela Gaspar | Colour photography |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA522241A (en) * | 1956-02-28 | Steinemann Willy | Azo dyestuffs | |
| GB541073A (en) * | 1940-04-09 | 1941-11-12 | Eastman Kodak Co | Process of colour photography and materials therefor |
| US2322001A (en) * | 1940-10-10 | 1943-06-15 | Eastman Kodak Co | Method of producing dye images |
| US2673198A (en) * | 1950-06-23 | 1954-03-23 | Sandoz Ag | Polyazo dyestuffs |
-
0
- NL NL227619D patent/NL227619A/xx unknown
- US US2899305D patent/US2899305A/en not_active Expired - Lifetime
- BE BE567518D patent/BE567518A/xx unknown
- NL NL106253D patent/NL106253C/xx active
-
1957
- 1957-05-09 GB GB14809/57A patent/GB841300A/en not_active Expired
-
1958
- 1958-04-18 CH CH5848558A patent/CH373640A/de unknown
- 1958-05-08 DE DEG24496A patent/DE1051635B/de active Pending
- 1958-05-09 FR FR1206766D patent/FR1206766A/fr not_active Expired
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB496559A (en) * | 1936-05-30 | 1938-11-30 | Bela Gaspar | Process for the manufacture of coloured photographic materials |
| GB520529A (en) * | 1938-08-06 | 1940-04-26 | Bela Gaspar | Process for producing colour photographs |
| US2514234A (en) * | 1939-08-09 | 1950-07-04 | Chromogen Inc | Process for the manufacture of color photographic images |
| DE740708C (de) * | 1940-05-07 | 1943-10-27 | Kodak Ag | Verfahren zur Erzeugung von lichtempfindlichen Schichten fuer das Silberblechverfahren |
| GB705171A (en) * | 1950-01-06 | 1954-03-10 | Bela Gaspar | Colour photography |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1167651B (de) * | 1961-01-26 | 1964-04-09 | Ciba Geigy | Photographische Schicht fuer das Silberfarbbleichverfahren |
| DE1165998B (de) * | 1961-09-27 | 1964-03-19 | Ciba Geigy | Photographische Schichten fuer das Silberfarbbleichverfahren |
| DE1285880B (de) * | 1962-12-11 | 1968-12-19 | Ciba Geigy | Photographische Materialien fuer das Silberfarbbleichverfahren |
Also Published As
| Publication number | Publication date |
|---|---|
| US2899305A (en) | 1959-08-11 |
| NL227619A (US06368395-20020409-C00050.png) | |
| GB841300A (en) | 1960-07-13 |
| BE567518A (US06368395-20020409-C00050.png) | |
| FR1206766A (fr) | 1960-02-11 |
| NL106253C (US06368395-20020409-C00050.png) | |
| CH373640A (de) | 1963-11-30 |
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