GB1377697A - Disazo dyestuffs their preparation and use in photographic materials - Google Patents
Disazo dyestuffs their preparation and use in photographic materialsInfo
- Publication number
- GB1377697A GB1377697A GB1474172A GB1474172A GB1377697A GB 1377697 A GB1377697 A GB 1377697A GB 1474172 A GB1474172 A GB 1474172A GB 1474172 A GB1474172 A GB 1474172A GB 1377697 A GB1377697 A GB 1377697A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bis
- give
- chloroformyl
- ethane
- carboxy
- 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
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 title 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 6
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 6
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 abstract 2
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 abstract 1
- AJHPGXZOIAYYDW-UHFFFAOYSA-N 3-(2-cyanophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid Chemical compound CC(C)(C)OC(=O)NC(C(O)=O)CC1=CC=CC=C1C#N AJHPGXZOIAYYDW-UHFFFAOYSA-N 0.000 abstract 1
- GBKBAXRLGXLFPA-UHFFFAOYSA-N 4-[2-(4-carbonochloridoylphenoxy)ethoxy]benzoyl chloride Chemical compound C1=CC(C(=O)Cl)=CC=C1OCCOC1=CC=C(C(Cl)=O)C=C1 GBKBAXRLGXLFPA-UHFFFAOYSA-N 0.000 abstract 1
- VAXBLYWAVAIJJJ-UHFFFAOYSA-N 4-[2-(4-carboxyphenoxy)ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCOC1=CC=C(C(O)=O)C=C1 VAXBLYWAVAIJJJ-UHFFFAOYSA-N 0.000 abstract 1
- VPUFWUGWXMKIKA-UHFFFAOYSA-N 4-[2-[(4-carbonochloridoylbenzoyl)amino]ethylcarbamoyl]benzoyl chloride Chemical compound ClC(=O)C1=CC=C(C(=O)NCCNC(C2=CC=C(C=C2)C(=O)Cl)=O)C=C1 VPUFWUGWXMKIKA-UHFFFAOYSA-N 0.000 abstract 1
- WBYJBCBKDGJMCI-UHFFFAOYSA-N 4-[2-[(4-carboxybenzoyl)amino]ethylcarbamoyl]benzoic acid Chemical compound C(=O)(O)C1=CC=C(C(=O)NCCNC(C2=CC=C(C=C2)C(=O)O)=O)C=C1 WBYJBCBKDGJMCI-UHFFFAOYSA-N 0.000 abstract 1
- OKIFHHUBCATEKX-UHFFFAOYSA-N 4-[3-(4-carbonochloridoylbenzoyl)benzoyl]benzoyl chloride Chemical compound C1=CC(C(=O)Cl)=CC=C1C(=O)C1=CC=CC(C(=O)C=2C=CC(=CC=2)C(Cl)=O)=C1 OKIFHHUBCATEKX-UHFFFAOYSA-N 0.000 abstract 1
- ADWVJWLBIORHFO-UHFFFAOYSA-N 4-[3-(4-carboxybenzoyl)benzoyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C(=O)C1=CC=CC(C(=O)C=2C=CC(=CC=2)C(O)=O)=C1 ADWVJWLBIORHFO-UHFFFAOYSA-N 0.000 abstract 1
- LKYGFDGSOYBOLS-UHFFFAOYSA-N 4-methoxycarbonylbenzoic acid;hydrochloride Chemical compound Cl.COC(=O)C1=CC=C(C(O)=O)C=C1 LKYGFDGSOYBOLS-UHFFFAOYSA-N 0.000 abstract 1
- NQUVCRCCRXRJCK-UHFFFAOYSA-N 4-methylbenzoyl chloride Chemical compound CC1=CC=C(C(Cl)=O)C=C1 NQUVCRCCRXRJCK-UHFFFAOYSA-N 0.000 abstract 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 1
- FIALLYBQVILKOF-UHFFFAOYSA-N [3-(4-methylbenzoyl)phenyl]-(4-methylphenyl)methanone Chemical compound C1=CC(C)=CC=C1C(=O)C1=CC=CC(C(=O)C=2C=CC(C)=CC=2)=C1 FIALLYBQVILKOF-UHFFFAOYSA-N 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- LOCJPOYKBUUVKU-UHFFFAOYSA-N methyl 3-amino-4-chlorobenzoate Chemical compound COC(=O)C1=CC=C(Cl)C(N)=C1 LOCJPOYKBUUVKU-UHFFFAOYSA-N 0.000 abstract 1
- BBCJQHYOGQEOAA-UHFFFAOYSA-N methyl 4-[2-(4-methoxycarbonylphenoxy)ethoxy]benzoate Chemical compound C1=CC(C(=O)OC)=CC=C1OCCOC1=CC=C(C(=O)OC)C=C1 BBCJQHYOGQEOAA-UHFFFAOYSA-N 0.000 abstract 1
- ZVJNDEOCNHLFIR-UHFFFAOYSA-N methyl 4-[2-[(4-methoxycarbonylbenzoyl)amino]ethylcarbamoyl]benzoate Chemical compound C1=CC(C(=O)OC)=CC=C1C(=O)NCCNC(=O)C1=CC=C(C(=O)OC)C=C1 ZVJNDEOCNHLFIR-UHFFFAOYSA-N 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G17/00—Electrographic processes using patterns other than charge patterns, e.g. an electric conductivity pattern; Processes involving a migration, e.g. photoelectrophoresis, photoelectrosolography; Processes involving a selective transfer, e.g. electrophoto-adhesive processes; Apparatus essentially involving a single such process
- G03G17/02—Electrographic processes using patterns other than charge patterns, e.g. an electric conductivity pattern; Processes involving a migration, e.g. photoelectrophoresis, photoelectrosolography; Processes involving a selective transfer, e.g. electrophoto-adhesive processes; Apparatus essentially involving a single such process with electrolytic development
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/08—Preparation of azo dyes from other azo compounds by reduction
- C09B43/085—Preparation of azo dyes from other azo compounds by reduction by reacting nitro azo dyes with amine or amino azo dye with nitro compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
- C09B43/136—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents
- C09B43/145—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents with polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
- C09B43/136—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents
- C09B43/16—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents linking amino-azo or cyanuric acid residues
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B45/00—Complex metal compounds of azo dyes
-
- 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
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Molecular Biology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH720871A CH566029A5 (enrdf_load_stackoverflow) | 1971-05-14 | 1971-05-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1377697A true GB1377697A (en) | 1974-12-18 |
Family
ID=4321562
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1474172A Expired GB1377697A (en) | 1971-05-14 | 1972-03-29 | Disazo dyestuffs their preparation and use in photographic materials |
| GB2054472A Expired GB1384162A (en) | 1971-05-14 | 1972-05-03 | Disazo dyestuffs their manufacture and use in photographic materials |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2054472A Expired GB1384162A (en) | 1971-05-14 | 1972-05-03 | Disazo dyestuffs their manufacture and use in photographic materials |
Country Status (9)
| Country | Link |
|---|---|
| JP (1) | JPS5529419B1 (enrdf_load_stackoverflow) |
| AT (1) | AT321718B (enrdf_load_stackoverflow) |
| BE (1) | BE783388A (enrdf_load_stackoverflow) |
| CA (1) | CA987309A (enrdf_load_stackoverflow) |
| CH (1) | CH566029A5 (enrdf_load_stackoverflow) |
| DE (1) | DE2223311A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2137637B1 (enrdf_load_stackoverflow) |
| GB (2) | GB1377697A (enrdf_load_stackoverflow) |
| IT (1) | IT957826B (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4314816A (en) | 1980-05-30 | 1982-02-09 | Mobay Chemical Corporation | Direct blue dyes from the condensation of diaminostilbenedisulfonic acid with N-alkyl or N-hydroxyalkyl-8-amino-1-naphthol-3,6-disulfonic acid |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL284975A (enrdf_load_stackoverflow) * | 1961-11-02 |
-
1971
- 1971-05-14 CH CH720871A patent/CH566029A5/xx not_active IP Right Cessation
-
1972
- 1972-03-29 GB GB1474172A patent/GB1377697A/en not_active Expired
- 1972-03-30 CA CA138,613A patent/CA987309A/en not_active Expired
- 1972-05-03 GB GB2054472A patent/GB1384162A/en not_active Expired
- 1972-05-08 FR FR7216407A patent/FR2137637B1/fr not_active Expired
- 1972-05-12 BE BE783388A patent/BE783388A/xx unknown
- 1972-05-12 AT AT414472A patent/AT321718B/de not_active IP Right Cessation
- 1972-05-12 IT IT5020972A patent/IT957826B/it active
- 1972-05-12 DE DE19722223311 patent/DE2223311A1/de not_active Withdrawn
- 1972-05-13 JP JP4758472A patent/JPS5529419B1/ja active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4314816A (en) | 1980-05-30 | 1982-02-09 | Mobay Chemical Corporation | Direct blue dyes from the condensation of diaminostilbenedisulfonic acid with N-alkyl or N-hydroxyalkyl-8-amino-1-naphthol-3,6-disulfonic acid |
Also Published As
| Publication number | Publication date |
|---|---|
| CH566029A5 (enrdf_load_stackoverflow) | 1975-08-29 |
| BE783388A (fr) | 1972-11-13 |
| GB1384162A (en) | 1975-02-19 |
| AT321718B (de) | 1975-04-10 |
| DE2223311A1 (de) | 1972-11-30 |
| JPS5529419B1 (enrdf_load_stackoverflow) | 1980-08-04 |
| IT957826B (it) | 1973-10-20 |
| FR2137637A1 (enrdf_load_stackoverflow) | 1972-12-29 |
| FR2137637B1 (enrdf_load_stackoverflow) | 1978-02-03 |
| CA987309A (en) | 1976-04-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |