GB1080252A - Improvements relating to reactive disazo dyestuffs and their use - Google Patents
Improvements relating to reactive disazo dyestuffs and their useInfo
- Publication number
- GB1080252A GB1080252A GB4286564A GB4286564A GB1080252A GB 1080252 A GB1080252 A GB 1080252A GB 4286564 A GB4286564 A GB 4286564A GB 4286564 A GB4286564 A GB 4286564A GB 1080252 A GB1080252 A GB 1080252A
- Authority
- GB
- United Kingdom
- Prior art keywords
- radical
- group
- halogeno
- hydrogen
- alkyl
- 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
- C09B62/002—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
- C09B62/01—Disazo or polyazo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
The invention comprises reactive dyestuffs of general formula <FORM:1080252/C4-C5/1> wherein D is a sulphonated benzene or naphthalene radical containing neither hydroxyl or acylatable amino groups, Y1 is hydrogen or a C1-C2 alkyl or alkoxy group; Y2 is hydrogen, C1-C2 alkyl or alkoxy group or an acylamino group; R is hydrogen or a C1-C2 alkyl group; Z is a reactive acyl radical capable of reacting with cellulose and polyamide fibrous material to form a chemical bond and is an a - or b -halogeno-alkanoyl radical, an a - or b -halogeno- or an a ,b -di-halogeno-alkenoyl radical, an a ,b -alkenoyl radical, an a ,b -alkynoyl radical, a halogeno-nitrobenzene carboxylic or sulphonic acid radical in which the halogen is o and/or p to the nitro group or groups, or a mono or dicyclic radical comprising a 5- or 6-membered heterocyclic ring of aromatic character having at least one reactive grouping <FORM:1080252/C4-C5/2> which forms part of the heterocycle and ring A may also contain a sulphonic acid group. Preferably, D is a naphthalene 1-sulphonic 2-azo radical having 1 or 2 additional sulphonic acid groups. They are prepared by acylating the corresponding amino substituted disazo dye to introduce the Z radical or alternatively the diazonium compound of an amine D-NH2 is coupled with an appropriate coupling component. Conventional condensing and coupling procedures are used. The reactive dye products dye staple fibre, jute, ramie, hemp, cotton, wool, silk and synthetic polyamides, e.g. nylon in orange-red shades.ALSO:Staple fibre, jute, ramie, hemp, cotton, mercerised cotton, wool silk, and synthetic polyamides, e.g. nylon are dyed in orange-red shades using reactive disazo-dyes of the general formula <FORM:1080252/D1-D2/1> wherein D is a sulphonated benzene or naphthalene radical free from hydroxyl and acylatable amino groups, Y1 is hydrogen or a C1-C2 alkyl or alkoxy group; Y2 is hydrogen, a C1-C2 alkyl or alkoxy group or an acylamino group; R is hydrogen or a C1-C2 alkyl group and Z is a reactive acyl radical capable of reacting with cellulose or polyamide fibrous material to form a chemical bond, e.g. an a or b -halogen-alkanoyl radical; a or b halogeno or a , b dihalogeno-alkenoyl radical; a or b alkenoyl or alkynoyl radical, a halogeno-nitrobenzene carboxylic or sulphonic acid radical wherein the halogen is o and/or p to the nitro group or groups or is a mono or dicyclic radical comprising a 5 or 6 membered ring having at least one <FORM:1080252/D1-D2/2> group which forms part of the heterocycle.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1296563A CH430003A (en) | 1963-10-22 | 1963-10-22 | Process for the preparation of reactive disazo dyes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1080252A true GB1080252A (en) | 1967-08-23 |
Family
ID=4388041
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4286564A Expired GB1080252A (en) | 1963-10-22 | 1964-10-21 | Improvements relating to reactive disazo dyestuffs and their use |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE654651A (en) |
CH (1) | CH430003A (en) |
FR (1) | FR1422175A (en) |
GB (1) | GB1080252A (en) |
NL (1) | NL6412258A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5686584A (en) * | 1994-11-17 | 1997-11-11 | Ciba-Geigy Corporation | Reactive dyes, their preparation, and their use |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1515030A (en) * | 1976-02-11 | 1978-06-21 | Ici Ltd | Fibre reactive disazo dyestuffs |
-
1963
- 1963-10-22 CH CH1296563A patent/CH430003A/en unknown
-
1964
- 1964-10-21 GB GB4286564A patent/GB1080252A/en not_active Expired
- 1964-10-21 NL NL6412258A patent/NL6412258A/xx unknown
- 1964-10-21 BE BE654651D patent/BE654651A/xx unknown
- 1964-10-22 FR FR992262A patent/FR1422175A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5686584A (en) * | 1994-11-17 | 1997-11-11 | Ciba-Geigy Corporation | Reactive dyes, their preparation, and their use |
Also Published As
Publication number | Publication date |
---|---|
FR1422175A (en) | 1965-12-24 |
BE654651A (en) | 1965-04-21 |
CH430003A (en) | 1967-02-15 |
NL6412258A (en) | 1965-04-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ES437447A1 (en) | Arylazoarylazo-substituted azo, azomethine 1:2 chromium complex dyes | |
GB1080252A (en) | Improvements relating to reactive disazo dyestuffs and their use | |
ES454384A1 (en) | Fibre-reactive azo dyes containing a monofluororotriazine group | |
GB1243941A (en) | Disazo dyestuffs | |
JPS5599967A (en) | Disazo dye for cellulose-containing fibers | |
GB1470633A (en) | Soluble trisazo dyestuffs and their production and use | |
GB1080056A (en) | 1:2-chromium-complexes of a reactive disazo dye and a monoazo dye and their use | |
GB952061A (en) | Novel disazo compounds | |
GB1061268A (en) | New water-insoluble azo dyestuffs | |
GB1458491A (en) | Reactive disazo dyestuffs | |
GB1460494A (en) | Disazo reactive dyestuffs | |
GB994502A (en) | New reactive monoazo dyestuffs and their use | |
GB944250A (en) | Improvements in and relating to the manufacture of azo dyes and the dyeing of synthetic thermoplastic material therewith | |
GB1039928A (en) | Reactive monoazo dyestuffs containing a benzene sulphonanilide group | |
GB1039379A (en) | Reactive dyestuffs containing a quinoxaline nucleus | |
GB1083793A (en) | Water-soluble reactive dyes | |
GB929426A (en) | New triazine azo dyestuffs | |
GB1470483A (en) | Soluble trisazo dyestuffs and their prod and use | |
GB949502A (en) | New azophthalocyanine dyestuffs and their manufacture and use | |
GB991793A (en) | Water-soluble reactive disazo dyes | |
GB1033264A (en) | Reactive monoazo dyestuffs containing triazole residues and their use | |
GB1330582A (en) | Fibre-reacrive copper-complex monoazo dyestuffs | |
US2049433A (en) | Coloring of materials made with or containing cellulose derivatives | |
GB707488A (en) | Manufacture of new disazo-dyestuffs | |
GB901692A (en) | New monoazo dyestuffs containing sulphonoxy groups, their preparation and their application to dyeing |