GB923148A - New anthraquinone dyestuffs - Google Patents
New anthraquinone dyestuffsInfo
- Publication number
- GB923148A GB923148A GB1055260A GB1055260A GB923148A GB 923148 A GB923148 A GB 923148A GB 1055260 A GB1055260 A GB 1055260A GB 1055260 A GB1055260 A GB 1055260A GB 923148 A GB923148 A GB 923148A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- formula
- hydrogen
- group
- 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
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
- C09B62/004—Anthracene dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
The invention comprises dyes of the formula <FORM:0923148/IV(a)/1> where the ring A may contain a sulphonic acid group or up to two halogen atoms, the ring B may be substituted by halogen, alkoxy, alkyl, sulphonic acid or carboxylic acid, n and m are each 0 or 1, Y is -SO2-,-CO- or -NR2CO-where R2 is hydrogen or alkyl the carbonyl being attached to the alkylene radical, R and R1 are each hydrogen, alkyl, hydroxyalkyl, sulphatoalkyl, sulphoalkyl, cycloalkyl, aralkyl, sulphonated aralkyl, aryl or substituted aryl, X is a divalent aliphatic radical or for an aromatic radical if neither R nor R1 is aromatic, and Z is an aryl radical which contain a group capable of reaction with cellulose fibre to form a covalent bond. Specified acyl radicals are those of acrylic, a -chloracrylic, propiolic, maleic, mono- and dichloromaleic, chloroacetic, sulphochloroacetic, b -chloro- and b -bromopropionic and a :b -dichloropropionic acids and radicals derived by reaction of one of the halogen atoms of 2:4:6-tribromo- and trichloro-pyrimidine, 2:4:5:6-tetrachloropyrimidine 5-methyl-, 5-nitro- and 5-cyano-2:4:6-trichloropyrimidine, 5-carboxy-, 5-carboethoxy-, 5-nitro-6-methyl- and 5-nitro-2:4-dichloropyrimidine, cyanuric bromide, cyanuric chloride and primary condensation products of cyanuric chloride or bromide with ammonia, methanol, ethanol, isopropanol, phenol, o-, m- and p-chlorophenol, o-, m- and p-cresol, o-, m- and p-sulphophenol, thiophenol, thioglycollic acid, diethyldithiocarbamic acid, mercaptobenzthiazole, methyl-, dimethyl-, ethyl-, diethyl-, n-propyl-, isopropyl-, butyl-, hexyl- and cyclohexyl-amine, toluidine, piperidine, morpholine, methoxyethylamine, ethanolamine, aminoacetic acid, aniline-2:5-disulphonic acid, orthanilic, metanilic and sulphanilic acid, 2-, 3- and 4-aminobenzoic acid, 5-amino-2-hydroxybenzoic acid, 2-aminoethane-sulphonic acid, aminonaphthalene mono- and di-sulphonic acid and N-methylaminoethane sulphonic acid. The dyes are made by acylating compounds of the above formula where Z is hydrogen and A, B, X, Y, R, R1, m and n are as above with an anhydride or acid halide of an acid containing a group capable of reacting with cellulose fibres. The compounds where Z is hydrogen are made by reacting compounds of the formulae <FORM:0923148/IV(a)/2> or <FORM:0923148/IV(a)/3> where A, B, Y and n are as above, Q is halogen, an esterified hydroxyl group or -S-Z where Z is a heterocycle or a negatively substituted phenyl group and Q1 is an alkenyl group having the unsaturated link in a :b -position to Y, with a compound of the formula <FORM:0923148/IV(a)/4> and if desired sulphating or sulphonating the products, or by condensing a compound of the formula <FORM:0923148/IV(a)/5> where P is chlorine or bromine, with an amine of the formula <FORM:0923148/IV(a)/6> Examples are given. The dyes dye and print cotton, viscose rayon, regenerated cellulose, wool, silk, cellulose acetate, polyamides, polyacrylonitrile and aromatic polyester fibres and dye and print cellulose fibres in conjunction with an acid-binding agent. Specifications 822,047, 848,742, 867,571, 885,059, 885,547, 885,814, 885,815, 887,723, 891,601 and 917,780 are referred to.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1055260A GB923148A (en) | 1960-03-24 | 1960-03-24 | New anthraquinone dyestuffs |
CH340061A CH419397A (en) | 1960-03-24 | 1961-03-22 | Process for the production of new anthraquinone dyes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1055260A GB923148A (en) | 1960-03-24 | 1960-03-24 | New anthraquinone dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB923148A true GB923148A (en) | 1963-04-10 |
Family
ID=9969940
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1055260A Expired GB923148A (en) | 1960-03-24 | 1960-03-24 | New anthraquinone dyestuffs |
Country Status (2)
Country | Link |
---|---|
CH (1) | CH419397A (en) |
GB (1) | GB923148A (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002348492A (en) * | 2001-05-24 | 2002-12-04 | Nippon Kagaku Kogyosho:Kk | Novel cationic dye |
CN106496489A (en) * | 2016-11-11 | 2017-03-15 | 清华大学 | Water-soluble colour chain extender, copoly type colorful polyurethane emulsion and colour polyurethane acrylate copolymer emulsion and preparation method |
US9852846B2 (en) | 2015-02-26 | 2017-12-26 | Capacitor Sciences Incorporated | Self-healing capacitor and methods of production thereof |
US9899150B2 (en) | 2014-05-12 | 2018-02-20 | Capacitor Sciences Incorporated | Energy storage device and method of production thereof |
US9932358B2 (en) | 2015-05-21 | 2018-04-03 | Capacitor Science Incorporated | Energy storage molecular material, crystal dielectric layer and capacitor |
US9941051B2 (en) | 2015-06-26 | 2018-04-10 | Capactor Sciences Incorporated | Coiled capacitor |
US9978517B2 (en) | 2016-04-04 | 2018-05-22 | Capacitor Sciences Incorporated | Electro-polarizable compound and capacitor |
US10026553B2 (en) * | 2015-10-21 | 2018-07-17 | Capacitor Sciences Incorporated | Organic compound, crystal dielectric layer and capacitor |
US10153087B2 (en) | 2016-04-04 | 2018-12-11 | Capacitor Sciences Incorporated | Electro-polarizable compound and capacitor |
US10305295B2 (en) | 2016-02-12 | 2019-05-28 | Capacitor Sciences Incorporated | Energy storage cell, capacitive energy storage module, and capacitive energy storage system |
US10340082B2 (en) | 2015-05-12 | 2019-07-02 | Capacitor Sciences Incorporated | Capacitor and method of production thereof |
US10395841B2 (en) | 2016-12-02 | 2019-08-27 | Capacitor Sciences Incorporated | Multilayered electrode and film energy storage device |
-
1960
- 1960-03-24 GB GB1055260A patent/GB923148A/en not_active Expired
-
1961
- 1961-03-22 CH CH340061A patent/CH419397A/en unknown
Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002348492A (en) * | 2001-05-24 | 2002-12-04 | Nippon Kagaku Kogyosho:Kk | Novel cationic dye |
US10685782B2 (en) | 2014-05-12 | 2020-06-16 | Capacitor Sciences Incorporated | Capacitor and method of production thereof |
US9899150B2 (en) | 2014-05-12 | 2018-02-20 | Capacitor Sciences Incorporated | Energy storage device and method of production thereof |
US10347424B2 (en) | 2014-05-12 | 2019-07-09 | Capacitor Sciences Incorporated | Energy storage device and method of production thereof |
US9852846B2 (en) | 2015-02-26 | 2017-12-26 | Capacitor Sciences Incorporated | Self-healing capacitor and methods of production thereof |
US10340082B2 (en) | 2015-05-12 | 2019-07-02 | Capacitor Sciences Incorporated | Capacitor and method of production thereof |
US9932358B2 (en) | 2015-05-21 | 2018-04-03 | Capacitor Science Incorporated | Energy storage molecular material, crystal dielectric layer and capacitor |
US9941051B2 (en) | 2015-06-26 | 2018-04-10 | Capactor Sciences Incorporated | Coiled capacitor |
US10672561B2 (en) | 2015-06-26 | 2020-06-02 | Capacitor Sciences Incorporated | Coiled capacitor |
US10854386B2 (en) | 2015-06-26 | 2020-12-01 | Capacitor Sciences Incorporated | Coiled capacitor |
US10026553B2 (en) * | 2015-10-21 | 2018-07-17 | Capacitor Sciences Incorporated | Organic compound, crystal dielectric layer and capacitor |
US10305295B2 (en) | 2016-02-12 | 2019-05-28 | Capacitor Sciences Incorporated | Energy storage cell, capacitive energy storage module, and capacitive energy storage system |
US10153087B2 (en) | 2016-04-04 | 2018-12-11 | Capacitor Sciences Incorporated | Electro-polarizable compound and capacitor |
US9978517B2 (en) | 2016-04-04 | 2018-05-22 | Capacitor Sciences Incorporated | Electro-polarizable compound and capacitor |
US10672560B2 (en) | 2016-04-04 | 2020-06-02 | Capacitor Sciences Incorporated | Electro-polarizable compound and capacitor |
US10707019B2 (en) | 2016-04-04 | 2020-07-07 | Capacitor Science Incorporated | Electro-polarizable compound and capacitor |
CN106496489B (en) * | 2016-11-11 | 2019-04-23 | 清华大学 | Water-soluble colour chain extender, copoly type colorful polyurethane emulsion and colour polyurethane-acrylate copolymer emulsion and preparation method |
CN106496489A (en) * | 2016-11-11 | 2017-03-15 | 清华大学 | Water-soluble colour chain extender, copoly type colorful polyurethane emulsion and colour polyurethane acrylate copolymer emulsion and preparation method |
US10395841B2 (en) | 2016-12-02 | 2019-08-27 | Capacitor Sciences Incorporated | Multilayered electrode and film energy storage device |
Also Published As
Publication number | Publication date |
---|---|
CH419397A (en) | 1966-08-31 |
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