GB1013580A - Reactive monazo dyestuffs and copper complexes thereof - Google Patents

Reactive monazo dyestuffs and copper complexes thereof

Info

Publication number
GB1013580A
GB1013580A GB1427164A GB1427164A GB1013580A GB 1013580 A GB1013580 A GB 1013580A GB 1427164 A GB1427164 A GB 1427164A GB 1427164 A GB1427164 A GB 1427164A GB 1013580 A GB1013580 A GB 1013580A
Authority
GB
United Kingdom
Prior art keywords
dyes
acid
reactive
copper complexes
cellulose
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
GB1427164A
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.)
Bayer AG
Original Assignee
Bayer 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 Bayer AG filed Critical Bayer AG
Publication of GB1013580A publication Critical patent/GB1013580A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/44—Oxygen and nitrogen or sulfur and nitrogen atoms
    • C07D231/46—Oxygen atom in position 3 or 5 and nitrogen atom in position 4
    • 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
    • C09B62/006—Azodyes
    • C09B62/0067—Azodyes with heterocyclic compound as coupling component

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention comprises azo dyes of formula <FORM:1013580/C4-C5/1> wherein A is an aromatic radical which may contain, in ortho-position to the azo group, a metallizable substituent or one which is convertible thereto under metallizing conditions and X is a reactive group (i.e. reacting with the hydroxyl groups of cellulose to form a covalent bond) and copper complexes thereof. The dyes may be prepared by coupling a diazotized amine A-NH2 with 1-(61-aminonaphthyl-(21)-41, 81-disulphonic acid) - 3 - methyl - 5 - pyrazolone and condensing the aminoazo dye so formed with a bifunctional reactive component such as 2,3 -dichloroquinoxaline - 6 - carboxylic acid or sulphonic acid chloride, cyanuric chloride, tri-or tetra-chloropyrimidine and 2-methoxy- or -phenylmercapto - 4,6 - dichlorotriazine. The condensation step may precede the coupling reaction. The dyes may be coppered in usual manner before or after the condensation reaction. The dyes give yellow to red shades on cellulose materials in the presence of acid-binding agents. Specification 841,413 is referred to.
GB1427164A 1963-04-18 1964-04-07 Reactive monazo dyestuffs and copper complexes thereof Expired GB1013580A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF39504A DE1243801B (en) 1963-04-18 1963-04-18 Process for the production of azo dyes or their metal complex compounds

Publications (1)

Publication Number Publication Date
GB1013580A true GB1013580A (en) 1965-12-15

Family

ID=7097799

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1427164A Expired GB1013580A (en) 1963-04-18 1964-04-07 Reactive monazo dyestuffs and copper complexes thereof

Country Status (3)

Country Link
CH (1) CH464400A (en)
DE (1) DE1243801B (en)
GB (1) GB1013580A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB878726A (en) * 1959-04-10 1961-10-04 Ici Ltd New copper complexes of azo dyestuffs containing halogeno-ú=-triazinylamino groups

Also Published As

Publication number Publication date
DE1243801B (en) 1967-07-06
CH464400A (en) 1968-10-31

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