GB1242047A - Photographic silver dye-bleach material containing azo dyestuffs - Google Patents

Photographic silver dye-bleach material containing azo dyestuffs

Info

Publication number
GB1242047A
GB1242047A GB534469A GB534469A GB1242047A GB 1242047 A GB1242047 A GB 1242047A GB 534469 A GB534469 A GB 534469A GB 534469 A GB534469 A GB 534469A GB 1242047 A GB1242047 A GB 1242047A
Authority
GB
United Kingdom
Prior art keywords
acid
group
formula
aminonaphthalene
nitro
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
Application number
GB534469A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis AG
Original Assignee
Ciba Geigy AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG
Publication of GB1242047A publication Critical patent/GB1242047A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B43/00Preparation of azo dyes from other azo compounds
    • C09B43/12Preparation of azo dyes from other azo compounds by acylation of amino groups
    • C09B43/136Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C7/00Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
    • G03C7/28Silver dye bleach processes; Materials therefor; Preparing or processing such materials
    • G03C7/29Azo dyes therefor

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

1,242,047. Azo dyestuffs. CIBA-GEIGY A.G. 31 Jan., 1969 [2 Feb., 1968], No. 5344/69. Heading C4P. [Also in Division G2] The invention comprises azo dyes of the formula wherein A is a naphthalene residue attached at the 1-position to the azo group, at the 2-position to an amino group and in 8-position to a hydroxyl group and contains at least one sulphonic acid or sulphonamide group in 6-position; B is a naphthalene residue containing one or two sulphonic acid or sulphonamide groups; n is 1, 2, 3 or 4 and D is an n-valent acyl residue of an at least n-valent acylating agent, e.g. the group -CO-, -CS-, a diacyl residue of a dicarboxylic acid such as terephthalic or isophthalic acid, fumaric acid, glutaric acid, thiophene-2 :5- dicarboxylic acid, an azobenzene dicarboxylic acid or a cyanuric chloride or a dichlorotriazine derivative. The dyes are made (1) by reacting an amine of the formula with a halide of the acylating agent, e.g. in Example A 1 , 2-nitro-6-aminonaphthalene-4:8- disulphonic acid # 2-amino-8-hydroxynaphthalene-6-sulphonic acid, the nitro group is reduced and 2 moles of the product reacted with terephthaloyl chloride; or (2) by coupling diazonium salts of the formula with compounds of the formula A-H, e.g. in Example O, the reaction product of two moles of 2-nitro-6-aminonaphthalene-4 :8-disulphonic acid with terephthaloyl chloride is reduced to the amine which is diazotized and coupled with 1 - hydroxy - 3 - pyrrolidinosulphonyl - 7 - aminonaphthalene. Other examples are given.
GB534469A 1968-02-02 1969-01-31 Photographic silver dye-bleach material containing azo dyestuffs Expired GB1242047A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH161668A CH507532A (en) 1968-02-02 1968-02-02 Photographic material containing at least one azo dye

Publications (1)

Publication Number Publication Date
GB1242047A true GB1242047A (en) 1971-08-11

Family

ID=4214594

Family Applications (1)

Application Number Title Priority Date Filing Date
GB534469A Expired GB1242047A (en) 1968-02-02 1969-01-31 Photographic silver dye-bleach material containing azo dyestuffs

Country Status (5)

Country Link
BE (1) BE727738A (en)
CH (1) CH507532A (en)
DE (1) DE1900790A1 (en)
FR (1) FR2001183A1 (en)
GB (1) GB1242047A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4841027A (en) * 1981-05-14 1989-06-20 Sumitomo Chemical Company, Limited Process for preparing phenyl- and naphthylazo-aminonaphthol sulphonic acids

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH508225A (en) * 1969-02-13 1971-05-31 Ciba Geigy Ag Photographic material
EP0169808A3 (en) * 1984-07-24 1988-12-21 Ciba-Geigy Ag Uv-absorber compounds, method for their preparation and their use as image dyes in photographic materials for the silver dye-bleaching process
DE3775573D1 (en) * 1986-02-11 1992-02-13 Ilford Ag PHOTOGRAPHIC MATERIAL FOR THE SILVER COLORING METHOD.
WO1997019916A2 (en) * 1995-11-29 1997-06-05 Fuji Photo Film Co., Ltd. Bisazo compounds, intermediates thereof, process for synthesizing the same and therapeutic agent for viral infection containing the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4841027A (en) * 1981-05-14 1989-06-20 Sumitomo Chemical Company, Limited Process for preparing phenyl- and naphthylazo-aminonaphthol sulphonic acids

Also Published As

Publication number Publication date
CH507532A (en) 1971-05-15
DE1900790A1 (en) 1969-09-11
FR2001183A1 (en) 1969-09-26
BE727738A (en) 1969-07-31

Similar Documents

Publication Publication Date Title
ES378465A1 (en) Reactive disazo dyestuffs containing triazines
GB1165661A (en) Reactive Dyestuffs
US3691148A (en) Insoluble heterocyclic disazo dyes
GB1242047A (en) Photographic silver dye-bleach material containing azo dyestuffs
US2835663A (en) Copperable disazo dyestuffs
US3895004A (en) Disazo dyestuffs containing a heterocyclic bridging member
US3642764A (en) Disazo dyestuffs
US2391164A (en) Metallizable triazine azo dyestuffs
GB1160361A (en) New Metal-Complex Azo Dyestuffs
GB838311A (en) New copper-containing triazine monoazo dyestuffs
GB1439801A (en) Reactive azo dyestuffs
GB1458374A (en) 2-pyrazolin-5-one derivatives as colour couplers for magenta
US3443953A (en) Photographic materials for the silver dyestuff bleaching process
US3627747A (en) Mixed chromium complexes of a phenylazonaphthyl dyestuff and a phenylazophenyl dyestuff
US2665273A (en) Azo compounds
US1867088A (en) New water soluble diazo akino compounds
US1896450A (en) Disazo dyes
US3211718A (en) Azo dyes and intermediates therefor
US2636030A (en) Copper-containing disazo dyestuffs
US1858623A (en) Diazo-amino compounds
GB1508461A (en) Fibre-reactive polyazo dyes their manufacture and use
GB769163A (en) New hydrazone dyestuffs and process for making them
USRE23380E (en) Polyazo dyestuffs
US1871850A (en) New diazo-amino compounds
GB1163840A (en) New bis-formazane dyestuffs containing copper or nickel, their production and use