GB880886A - New azo dyestuffs containing sulphone radicals - Google Patents
New azo dyestuffs containing sulphone radicalsInfo
- 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
Links
Classifications
-
- 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
- C09B62/44—Reactive 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
- C09B62/503—Reactive 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
- C09B62/507—Azo 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.
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)
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 |
-
1959
- 1959-07-13 GB GB2394459A patent/GB880886A/en not_active Expired
-
1960
- 1960-07-13 CH CH798660A patent/CH393582A/en unknown
Cited By (1)
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 |
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