GB880886A - New azo dyestuffs containing sulphone radicals - Google Patents

New azo dyestuffs containing sulphone radicals

Info

Publication number
GB880886A
GB880886A GB2394459A GB2394459A GB880886A GB 880886 A GB880886 A GB 880886A GB 2394459 A GB2394459 A GB 2394459A GB 2394459 A GB2394459 A GB 2394459A GB 880886 A GB880886 A GB 880886A
Authority
GB
United Kingdom
Prior art keywords
amino
enylsulphonyl
dyes
aniline
chloro
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
GB2394459A
Inventor
Gerald Booth
Frank Hall
George Harold Keats
James Stuart Hunter
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB2394459A priority Critical patent/GB880886A/en
Priority to CH798660A priority patent/CH393582A/en
Publication of GB880886A publication Critical patent/GB880886A/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
    • C09B62/44Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
    • C09B62/503Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an esterified or non-esterified hydroxyalkyl sulfonyl or mercaptoalkyl sulfonyl group, a quaternised or non-quaternised aminoalkyl sulfonyl group, a heterylmercapto alkyl sulfonyl group, a vinyl sulfonyl or a substituted vinyl sulfonyl group, or a thiophene-dioxide group
    • C09B62/507Azo dyes

Landscapes

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

Abstract

The invention comprises disperse azo dyes of formula D-(SO2R)n where D is an azo dye residue, R is CH2. CHOH. CH2X, CH= CH. CH2OH or CH=CH.CH2X where X is Cl or Br and n is 1 or 2, provided that D is free from SO3H and COOH groups and that each of the SO2R groups is attached to a carbon atom of an aryl ring present in D. The dyes are made by conventional diazotisation and coupling processes. Representative of specified diazo components are aniline, 2-chloro-4-nitroaniline, 2 - amino - 5 - nitrobenzonitrile, p - aminobenzenesulphonamide, 4 - amino - 3 - chlorophenyl methyl sulphone, 2-amino-5-cyanobenzotrifluoride, 2-amino-5-nitrothiazole, 2-amino-6-methoxybenzthiazole, 4-(31-chloroprop-11,21-enylsulphonyl) aniline, 2-amino-4-(31-chloro-21-hydroxypropylsulphonyl) - anisole, 2 - chloro - 4 - (31-hydroxyprop - 11,21 - enylsulphonyl) aniline, 4 - amin - 2,5 - dimethoxy - 4 - nitroazobenzene and 6 - (31 - hydroxyprop - 11,21 - enylsulphonyl) - 2 - naphthylamine. Examples of specified coupling components are p-cresol, 2-hydroxy-5,6,7,8- tetrahydronaphthalene, 3-methyl-and-carbethoxy-5-pyrazolones, 1-o-phenyl-3-methyl-5-pyrazolone, 1 - [31-and 41 - (311 - chloro - 211 - hydroxypropylsulphonyl) - phenyl - 3 - methyl - 5 - pyrazolone, 3- and 4-(31-hydroxyprop-11,21-enylsulphonyl) -acetoacetanilide, 6 - (31 - chloroprop - 11, 21 - enylsulphonyl) - 2 - naphthol, 2 - hydroxy - 3 - naphthoic anilide, 1-carboethoxyamino-7-naphthol, 2,4-dihydroxyquinoline, barbituric acid, 1 - naphthylamine, N,N - di - (b - hydroxyethyl) aniline and 6-sulphonyl-2-naphthylamine. Preferred are dyes of formula A(SO2R)-N=N-E where A is a benzenic residue and E is a coupling component residue containing an amino, or substituted amino, group o or p to the azo group. The dyes colour textile materials comprising natural and synthetic fibres, e.g. polyamide, modified polyacrylonitrile, aromatic polyester, rayon, cellulose triacetate, wool and cellulosic fibres. Disperse colouring processes are used. Yellow to blue shades are obtained. Examples are provided of the preparation of the dyes and their use in colouring processes.
GB2394459A 1959-07-13 1959-07-13 New azo dyestuffs containing sulphone radicals Expired GB880886A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB2394459A GB880886A (en) 1959-07-13 1959-07-13 New azo dyestuffs containing sulphone radicals
CH798660A CH393582A (en) 1959-07-13 1960-07-13 Process for the production of azo dyes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2394459A GB880886A (en) 1959-07-13 1959-07-13 New azo dyestuffs containing sulphone radicals

Publications (1)

Publication Number Publication Date
GB880886A true GB880886A (en) 1961-10-25

Family

ID=10203852

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2394459A Expired GB880886A (en) 1959-07-13 1959-07-13 New azo dyestuffs containing sulphone radicals

Country Status (2)

Country Link
CH (1) CH393582A (en)
GB (1) GB880886A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5231171A (en) * 1990-12-24 1993-07-27 Basf Aktiengesellschaft Reactive dyes having an allylsulfonyl or propargylesulfonyl group

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5231171A (en) * 1990-12-24 1993-07-27 Basf Aktiengesellschaft Reactive dyes having an allylsulfonyl or propargylesulfonyl group

Also Published As

Publication number Publication date
CH393582A (en) 1965-06-15

Similar Documents

Publication Publication Date Title
GB909843A (en) New monoazo dyestuffs containing ester groups
GB880886A (en) New azo dyestuffs containing sulphone radicals
GB955085A (en) Improvements relating to monoazo aminopyrazole dyestuffs and their use
US2234723A (en) Azo compounds and material colored therewith
ES402665A1 (en) Monoazo dispersion dyes - from benzisothiazole diazo components for synthetic fibre
GB1039379A (en) Reactive dyestuffs containing a quinoxaline nucleus
US2412312A (en) Cellulose acetate dyed with monoazo dyes
US2032463A (en) Fibers dyed with water-insoluble azo-dyestuffs
US2113029A (en) Dyeing
US2383264A (en) Azo dyestuffs from 5-amino coumaran
GB924599A (en) New metal complex monoazo triazine dyestuffs
GB923887A (en) New monoazo triazine dyestuffs
ES254256A1 (en) Monoazophthalocyanine dyes
GB901692A (en) New monoazo dyestuffs containing sulphonoxy groups, their preparation and their application to dyeing
US2275124A (en) Azo dye
US4010151A (en) Water insoluble mono azo and disazo dyes containing cinnamonitrile group
US2307921A (en) Azo dyes
US2172753A (en) Dibazo dyes fob cellulose esters
DE1644109C3 (en) Water-insoluble nitromonoazo dyes and processes for dyeing polyester fibers
GB879263A (en) Monoazo dyestuffs containing halogenoacyl groups
GB902776A (en) Metal complexes of mixtures of monoazo-dyestuffs and process for their manufacture
Allen Miscellaneous dyes
GB868742A (en) New monoazo dyestuffs and the production of the same
GB731448A (en) Monoazo dyestuffs and process for their manufacture
GB762844A (en) Polyazo dyestuffs