ES251284A1 - Polyazo-dyestuffs derived from barbituric acid and process for their manufacture - Google Patents

Polyazo-dyestuffs derived from barbituric acid and process for their manufacture

Info

Publication number
ES251284A1
ES251284A1 ES0251284A ES251284A ES251284A1 ES 251284 A1 ES251284 A1 ES 251284A1 ES 0251284 A ES0251284 A ES 0251284A ES 251284 A ES251284 A ES 251284A ES 251284 A1 ES251284 A1 ES 251284A1
Authority
ES
Spain
Prior art keywords
dyes
group
residue
naphthalene
acid
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
ES0251284A
Other languages
Spanish (es)
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
BASF Schweiz AG
Original Assignee
Ciba Geigy AG
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 Geigy AG, Ciba AG filed Critical Ciba Geigy AG
Publication of ES251284A1 publication Critical patent/ES251284A1/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
    • C09B39/00Other azo dyes prepared by diazotising and coupling
    • 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
    • C09B31/00Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
    • C09B31/16Trisazo dyes
    • C09B31/26Trisazo dyes from other coupling components "D"
    • C09B31/28Heterocyclic compounds
    • 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
    • C09B35/00Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • C09B35/36Trisazo dyes of the type
    • 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
    • C09B45/02Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
    • C09B45/24Disazo or polyazo compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

The invention comprises dyes of formula <FORM:0902228/IV (b)/1> where R is the residue of a diazo component containing at least one azo group, and also contains a metallisable group in a vicinal position to the N=N-A group, and A is the residue of a naphthol sulphonic acid bound to R-N=N- vicinal to the hydroxy group the naphthalene nucleus of A being advantageously bound directly to the two azo links, and the heavy metal, especially copper, complexes of the dyes. The dyes are made by coupling barbituric acid with appropriate diazo components, or metal complexes thereof, the metal-free dyes being subsequently metallised if required. The dyes may also be made by coupling a diazo compound of an amine RNH2 with the necessary naphthol-azo-barbituric acid component with metallisation of the product if necessary. Preferred are dyes of formula <FORM:0902228/IV (b)/2> where m and n are 1 or 2, R1 and R3 are benzene or naphthalene residues and R2 is a benzene, naphthalene, diphenyl or 5-pyrazolone residue and especially dyes where m is 1, or is 2 and R2 is a 5-pyrazolone residue bound in the 4-position to the R3-N=N-group and in the 1-position through an arylene group to the -N=N-R1 group and particularly dyes of formula <FORM:0902228/IV (b)/3> where n is 1 or 2, R is a benzene or naphthalene residue and R2 is a benzene, diphenyl, naphthalene or 5-pyrazolone residue. Amongst indicated compounds from which R is derived are aminosalicyclic acid, aniline-2,5-disulphonic acid, nitro- and chloro-anilines, 4-amino- 41-acetylaminodiphenyl- 3-sulphonic acid, 2-naphthylamine-4,8-disulphonic acid, dehydrothiotoluidine mono- and di-sulphonic acids, aminoazobenzene mono- and di-sulphonic acids and compounds obtained by coupling the above azo group free amines with coupling components such as 3-methyl-aniline and 1-naphthylamine-6- and -7-sulphonic acids. R may also be derived from diamines such as 4,41-diamino-3,31-dimethoxy-diphenyl or from stilbene or triazole or acetoacet-anilide derivatives. The portion of the dye corresponding to R may also be metallised. Representative of indicated components corresponding to R1 are 2-methoxy-5-methyl-aniline and 2-methoxy-1-naphthylamine monosulphonic acids unsubstituted in the 4-position. Copper and nickel are specified metals. Hydroxyl, alkoxy and carboxy groups are specified metallisable groups. The dyes colour materials such as wool, silk and leather and especially cellulosic materials such as cotton, linen, artificial silk and regenerated cellulose fibres. The dyeings may be metallised on the fibre or in the dye-bath. Examples are provided of the preparation of the dyes and their use in colouring processes. Green and grey shades are obtained on cellulosic materials. Specifications 619,969, 644,883 and 744,666 are referred to.
ES0251284A 1958-08-06 1959-08-05 Polyazo-dyestuffs derived from barbituric acid and process for their manufacture Expired ES251284A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH6263458A CH369844A (en) 1958-08-06 1958-08-06 Process for the preparation of polyazo dyes

Publications (1)

Publication Number Publication Date
ES251284A1 true ES251284A1 (en) 1960-02-16

Family

ID=4524416

Family Applications (1)

Application Number Title Priority Date Filing Date
ES0251284A Expired ES251284A1 (en) 1958-08-06 1959-08-05 Polyazo-dyestuffs derived from barbituric acid and process for their manufacture

Country Status (4)

Country Link
CH (1) CH369844A (en)
DE (1) DE1135596B (en)
ES (1) ES251284A1 (en)
GB (1) GB902228A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH613468A5 (en) * 1975-07-31 1979-09-28 Ciba Geigy Ag
SG74532A1 (en) * 1994-09-16 2000-08-22 Sumitomo Chemical Co Tetrakisazo compound and a polarizing film containing the same
BR0311610A (en) 2002-06-06 2005-02-22 Ciba Sc Holding Ag Yellow anionic dyes
CN110079118A (en) * 2019-04-12 2019-08-02 上海应用技术大学 A kind of synthetic method of yellow Mono azo organic pigment

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2448158A (en) * 1945-01-04 1948-08-31 Du Pont Green tetrakisazo dyes

Also Published As

Publication number Publication date
GB902228A (en) 1962-08-01
DE1135596B (en) 1962-08-30
DE1135596C2 (en) 1963-03-21
CH369844A (en) 1963-06-15

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