GB1100574A - New anthraquinone dyestuffs and processes for their manufacture and use - Google Patents

New anthraquinone dyestuffs and processes for their manufacture and use

Info

Publication number
GB1100574A
GB1100574A GB29733/66A GB2973366A GB1100574A GB 1100574 A GB1100574 A GB 1100574A GB 29733/66 A GB29733/66 A GB 29733/66A GB 2973366 A GB2973366 A GB 2973366A GB 1100574 A GB1100574 A GB 1100574A
Authority
GB
United Kingdom
Prior art keywords
acid
compounds
carboxylic acid
dihalopropionic
formula
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
GB29733/66A
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.)
BASF Schweiz AG
Original Assignee
Ciba 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 AG filed Critical Ciba AG
Publication of GB1100574A publication Critical patent/GB1100574A/en
Expired legal-status Critical Current

Links

Classifications

    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01C—RESISTORS
    • H01C17/00—Apparatus or processes specially adapted for manufacturing resistors
    • H01C17/06—Apparatus or processes specially adapted for manufacturing resistors adapted for coating resistive material on a base
    • H01C17/075—Apparatus or processes specially adapted for manufacturing resistors adapted for coating resistive material on a base by thin film techniques
    • H01C17/14—Apparatus or processes specially adapted for manufacturing resistors adapted for coating resistive material on a base by thin film techniques by chemical deposition
    • H01C17/18—Apparatus or processes specially adapted for manufacturing resistors adapted for coating resistive material on a base by thin film techniques by chemical deposition without using electric current
    • 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
    • C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/002—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the linkage of the reactive group being alternatively specified
    • C09B62/004—Anthracene dyes
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
    • C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
    • C23C18/31—Coating with metals
    • C23C18/32—Coating with nickel, cobalt or mixtures thereof with phosphorus or boron
    • C23C18/34—Coating with nickel, cobalt or mixtures thereof with phosphorus or boron using reducing agents
    • C23C18/36—Coating with nickel, cobalt or mixtures thereof with phosphorus or boron using reducing agents using hypophosphites
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F13/00—Inhibiting corrosion of metals by anodic or cathodic protection
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors

Abstract

The invention comprises compounds of the formula <FORM:1100574/C4-C5/1> where Z is a sulphonic acid group; a, b, c and d are methyl groups and X is the residue of an a ,b -dihalopropionic acid, a -bromoacrylic acid, dichloroquinoxaline carboxylic acid, dichlorophthalazine carboxylic acid, dichloropyridazone propionic acid or 2-chlorobenzthiazole carboxylic acid. The compounds are prepared by treating compounds of the above formula wherein X is H with the corresponding acid halide, or with a ,b -dihalopropionic acid anhydride. The compounds of the above formula wherein X is a ,b -dibromopropionyl may be treated with an alkali to split off HBr giving the compounds wherein X is b -dibromoacrylyl.ALSO:Materials are dyed or printed with compounds of the formula <FORM:1100574/D1-D2/1> where Z is SO3H; a, b, c and d are methyl and X is the residue of an a , b -dihalopropionic acid, a -bromo-acrylic acid, dichloroquinoxaline carboxylic acid, dichlorophthalazine carboxylic acid, dichloropyridazone propionic acid or 2-chlorobenzthiazole carboxylic acid. An example describes the dyeing of wool knitting yarn from an aqueous dye bath containing sodium sulphate, acetic acid and an addition product of oleylamine and ethylene oxide.
GB29733/66A 1965-07-07 1966-07-01 New anthraquinone dyestuffs and processes for their manufacture and use Expired GB1100574A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH955865A CH461680A (en) 1965-07-07 1965-07-07 Process for the production of new anthraquinone dyes

Publications (1)

Publication Number Publication Date
GB1100574A true GB1100574A (en) 1968-01-24

Family

ID=4353228

Family Applications (1)

Application Number Title Priority Date Filing Date
GB29733/66A Expired GB1100574A (en) 1965-07-07 1966-07-01 New anthraquinone dyestuffs and processes for their manufacture and use

Country Status (6)

Country Link
BE (1) BE683735A (en)
CH (1) CH461680A (en)
DE (1) DE1644506B2 (en)
ES (1) ES328776A1 (en)
GB (1) GB1100574A (en)
NL (1) NL6609467A (en)

Also Published As

Publication number Publication date
DE1644506A1 (en) 1969-10-02
CH461680A (en) 1968-08-31
DE1644506B2 (en) 1975-03-06
NL6609467A (en) 1967-01-09
ES328776A1 (en) 1967-08-16
BE683735A (en) 1967-01-06

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