GB870985A - New complex metal compounds of monoazo-dyestuffs derived from cyanuric halides, their manufacture and use - Google Patents

New complex metal compounds of monoazo-dyestuffs derived from cyanuric halides, their manufacture and use

Info

Publication number
GB870985A
GB870985A GB25422/57A GB2542257A GB870985A GB 870985 A GB870985 A GB 870985A GB 25422/57 A GB25422/57 A GB 25422/57A GB 2542257 A GB2542257 A GB 2542257A GB 870985 A GB870985 A GB 870985A
Authority
GB
United Kingdom
Prior art keywords
dyes
sulphonic acid
naphthol
acid
complexes
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
GB25422/57A
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 GB870985A publication Critical patent/GB870985A/en
Priority claimed from CH1180064A external-priority patent/CH467321A/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
    • C09B62/00Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/02Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
    • C09B62/04Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to a triazine ring
    • C09B62/08Azo dyes
    • C09B62/095Metal complex azo dyes
    • 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
    • C09B45/00Complex metal compounds of azo dyes
    • C09B45/48Preparation from other complex metal compounds of azo dyes
    • 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
    • C09B67/00Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0032Treatment of phthalocyanine pigments
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J2893/00Discharge tubes and lamps
    • H01J2893/0072Disassembly or repair of discharge tubes
    • H01J2893/0073Discharge tubes with liquid poolcathodes; constructional details

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Coloring (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

870,985. Monoazo triazine dyes. CIBA Ltd. Aug. 12, 1957 [Aug. 10, 1956; Oct. 17, 1956; Jan. 25, 1957], No. 25422/57. Class 2(4). The invention comprises complex metal compounds of #, #<SP>1</SP>-dioxy-monoazo dyes which contain at least two, and advantageously more than two carboxylic or sulphonic acid groups and contain bound through an N bridge a residue of formula:- where R is NH 2 or the residue of an organic monoamine bound to C through its amino group and having at most 13 C atoms and, if it is aromatic, is substituted by at least one carboxylic or sulphonic acid group as the sole salt-forming substituent or substituents present. The dyes may be made by treating a 2, 4, 6-trihalogen- 1, 3, 5-triazine with an appropriate metalliferous aminoazo dye and treating the product, with or without isolation, with ammonia or an appropriate monoamine. In some instances they may be made by metallizing appropriate dyes, e.g. when the triazine halogen is not affected by the metallization process. The amino group in the dye residue may be obtained by reducing nitro or hydrolysing acylamino groups. Preferred classes of the dyes are copper complexes and 1, 2-chromium and cobalt complexes of dyes containing two sulphonic acid groups and of formula:- where R is a chloro- or nitro-benzene residue with OH #- to the azo group and X is an amino group. Preferably the triazine residue is in the coupling component moiety of the dye. Copper, chromium, cobalt, nickel, manganese, iron and aluminium complexes are mentioned. 1, 1-Complexes of copper and nickel and 1, 2-complexes of chromium and cobalt are preferred. Representative of specified or indicated amines from which R is derived are:-methyl-, methoxypropyl-, cyclohexyl-, diethyl- and chloroethyl-amines, ethanolamines, aminocarbonic acid esters, aminoacetic acid ethyl esters, aminoethane sulphonic acid, #-aminobenzoic acid, m-aminobenzene sulphonic acid and aminonaphthalene mono-, di- and tri-sulphonic acids. Representative of specified or indicated amines comprising the diazo component of the dyes are:-chloro- and nitro- #-amino-phenols and #-aminophenol, mono- or di-sulphonic acids and representative of coupling components specified and indicated are m-aminophenol, 1-(41-aminophenyl)- 3-methyl- 5-pyrazolone, #-ketocarboxylic acid arylamides, 2-amino- 8-naphthol- 6-, 2-alkylamino- 5-naphthol- 7-, 2-(3<SP>1</SP>-aminobenzoylamino)- 5-naphthol- 7- and 2-(4<SP>1</SP>-aminophenylamino)- 5-naphthol-3<SP>1</SP>, 7- di-sulphonic acids. The dyes colour polyhydroxylated fibrous materials, e.g. wood pulp, regenerated cellulose, viscose, linen and cotton, especially when used with alkalis. Examples are provided of the preparation of the dyes and their use in dyeing processes, representative of the diazo components used additional to those indicated above being -6-acetylamino- 2-aminophenol- 4-sulphonic acid, 4-methyl- 2-aminophenol- 5-sulphonic acid and 1-amino- 2- naphthol- 4-sulphonic acid and amongst the pyrazolone coupling components used is one of formula:- Specifications 299,331, 797,946, 851,537, 852,120 and 863,754 are referred to.
GB25422/57A 1956-08-10 1957-08-12 New complex metal compounds of monoazo-dyestuffs derived from cyanuric halides, their manufacture and use Expired GB870985A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH3640856 1956-08-10
CH1180064A CH467321A (en) 1964-09-10 1964-09-10 Process for the production of new azo dyes

Publications (1)

Publication Number Publication Date
GB870985A true GB870985A (en) 1961-06-21

Family

ID=32394641

Family Applications (2)

Application Number Title Priority Date Filing Date
GB25422/57A Expired GB870985A (en) 1956-08-10 1957-08-12 New complex metal compounds of monoazo-dyestuffs derived from cyanuric halides, their manufacture and use
GB3878465A Expired GB1108297A (en) 1956-08-10 1965-09-10 New reactive copper complex mono azo dyestuffs and processes for their manufacture and use

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB3878465A Expired GB1108297A (en) 1956-08-10 1965-09-10 New reactive copper complex mono azo dyestuffs and processes for their manufacture and use

Country Status (5)

Country Link
BE (2) BE559945A (en)
CH (4) CH354187A (en)
FR (2) FR1180975A (en)
GB (2) GB870985A (en)
NL (1) NL106787C (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH406480A (en) * 1960-01-29 1966-01-31 Sandoz Ag Process for the production of reactive dyes
DE3376318D1 (en) * 1982-06-22 1988-05-26 Bayer Ag NAPHTHOL AMINE DERIVATIVES
CN106854381A (en) * 2017-01-03 2017-06-16 上海安诺其集团股份有限公司 A kind of dye composite, its preparation method and application

Also Published As

Publication number Publication date
GB1108297A (en) 1968-04-03
FR88875E (en) 1967-04-07
NL106787C (en) 1963-12-16
FR1180975A (en) 1959-06-10
CH362472A (en) 1962-06-15
CH353474A (en) 1961-04-15
BE571893A (en) 1959-04-09
CH354187A (en) 1961-05-15
CH361068A (en) 1962-03-31
BE559945A (en) 1958-02-10

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