SU727664A1 - Ammonium or sulfonium derivative of 2,9-dichloromethylquinacrydone possessing properties of cyanal and cationic dye - Google Patents
Ammonium or sulfonium derivative of 2,9-dichloromethylquinacrydone possessing properties of cyanal and cationic dye Download PDFInfo
- Publication number
- SU727664A1 SU727664A1 SU782640878A SU2640878A SU727664A1 SU 727664 A1 SU727664 A1 SU 727664A1 SU 782640878 A SU782640878 A SU 782640878A SU 2640878 A SU2640878 A SU 2640878A SU 727664 A1 SU727664 A1 SU 727664A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- cyanal
- ammonium
- dichloromethylquinacrydone
- cationic dye
- sulfonium derivative
- Prior art date
Links
Landscapes
- Pyridine Compounds (AREA)
Description
1 г 2,9-дихлорметилхинакридона смешивали с 70 мл пиридина и кип тили с обратным холодильником в течение 8 . Выпавший после охлаждени Осадок фильтровали, промывали бензолом и ацетоном. Выход 89-90%. Элементный анализ1 g of 2,9-dichloromethylquinacridone was mixed with 70 ml of pyridine and heated under reflux for 8. Precipitated after cooling, the precipitate was filtered, washed with benzene and acetone. Yield 89-90%. Elemental analysis
Найдено, %: С 67,1; И 4,0; N 8,9 Cft 11 ,04.Found,%: C 67.1; And 4.0; N 8.9 Cft 11, 04.
CjjH, .Ctj.Cjjh, .ctj.
Вычислено/ %: С 67,6; Н 4,2; N9,,3.Calculated /%: C 67.6; H 4.2; N9, 3.
П р и м е р 2, Получение тиурони вой (сульфониевой) соли на основе 2, 9-дихлОрметилхинакрид6на.,,;.,.,...EXAMPLE 2, Preparation of Thiuronium (Sulfonium) Salt on the Basis of 2, 9-DichlOrmethylquinacrid6. ,, ,,.,., ...
1 г 2,9-дихлорметилхинакридона и 6/5 г тетгэаметилтиомочевнны тщательно растирают, смешивают с 30 мл воды и сплавл ют в фарфоровой чашке на кип щей вод ной бане до сухого остатка. Полученную соль охлаждают, разжижают 30 мл ацетона и фильтруют и вновь промывают ацетоном. Выход 90-92%. Элементный анализ. HfaUfleHO, %: С 56, 6; Н 5,6;Ы 11,1 S 9,0; се 9,65.1 g of 2,9-dichloromethylquinacridone and 6/5 g of tetheamethylthiourea are triturated, mixed with 30 ml of water and fused in a porcelain dish in a boiling water bath to a dry residue. The resulting salt is cooled, diluted with 30 ml of acetone and filtered and washed again with acetone. Yield 90-92%. Elemental analysis. HfaUfleHO,%: C 56, 6; H 5.6; S 11.1 S 9.0; All 9.65.
C,,,ce ,C ,,, ce,
Вычислено,: С57,0;Н5,6; N 12,3; S ,5; Си 10,5.Calculated: С57,0; Н5,6; N 12.3; S, 5; C 10.5.
Предлагаемые соединени вл ютс красител ми, окрашивающими в бордовый цвет.The proposed compounds are burgundy-colored dyes.
Крашение целлюлозно-бумажного волокна .Dyeing pulp and paper fiber.
Крашение ведут путем плюсовани ткани при 50-55°с раствором красител в воде (30-40 г/л), отжимают и пропускают через раствор соды .. (5 г/л) при 40°С, затем промывают гор чей и холодной водой. .Dyeing is carried out by padding the fabric at 50-55 ° with a dye solution in water (30-40 g / l), squeezing and passing through soda solution .. (5 g / l) at 40 ° C, then washed with hot and cold water . .
Оценка прочности, ба лEvaluation of strength, ball
КрасительDye
727664727664
Испытание прочности окрасок провод т по ГОСТУ 9733-61.Test the strength of the colors carried out according to GOST 9733-61.
Полученные выкраски показали высокие прочности к различным видам обработок.The obtained color showed high strength to various types of treatments.
Крашение полиакрилонитрильного волокна (нитрон).Dyeing polyacrylonitrile fiber (Nitron).
Крашение нитрона проводили из ванны, содержащей пропиленкарбонат (50 г/л). Модуль ванны 50. Образец помещали в красильную ванну при 5060 С на 15-20 мин, затем поднимали температуру до кипени и красили еие 1 ч. Окршиенный образец тщательно прмывали гор чей водой, раствором моющего средства, холодной водой и сушили. Испытание прочности окрасок щэоизводили по ГОСТУ 9733-61..Nitron was dyed from a bath containing propylene carbonate (50 g / l). Bath module 50. The sample was placed in a dye bath at 5060 C for 15–20 min, then the temperature was raised to a boil and dyed for 1 h. The painted sample was thoroughly washed with hot water, detergent solution, cold water, and dried. The test of the strength of the paint is produced according to GOST 9733-61 ..
Полученные выкраски имеют высокие показатели прочности к различным видам обработок.The obtained vykraski have high strength to various types of treatments.
Важным свойством синтезированных соединений вл етс высока прочност к химчистке, к стирке и свету, и что особенно ценно - универсальность применени . Они позвол ют проводить крашение как полиакрилонитрильного волокна (нитрона), так и хлопчатобумажной ткани непосредственно из водных растворов, с сохранением высоких прочностных свойств красителей к физико-химическим воздействи м (таблица). Это особенно важно с точк зрени применени к ткан м из смешанных волокон. An important property of the synthesized compounds is the high strength to dry cleaning, washing and light, and that the versatility of application is especially valuable. They allow dyeing both polyacrylonitrile fiber (Nitron) and cotton fabric directly from aqueous solutions, while maintaining the high strength properties of dyes to the physicochemical effects (table). This is especially important from the point of view of application to mixed-fiber fabrics.
Показатели прочности окрасок к физико-химическим воздействи м Приведены в таблице.Indicators of the strength of colors to physicochemical effects are given in the table.
Пиридиниёва Pyridiniev
соль на основеsalt based
2,9-дихлорметилхинакридона 2,9-dichloromethylquinacridone
Тиурониева ,: соль на основе 2, 9 -Ди . тилхинакридбна Tiuroniev, salt on the basis of 2, 9 -Di. tilhinacridbna
/ - X;Й:ЧЧ, -- ---г---- ------ - -И р И М ё ч а иri ё: Верхн цифра показывает прочность/ - X; Y: HH, - --- r ---- ------ - - And p And M y ch iri ri y: The upper figure shows the strength
окрасок на полиакрилонитрильном волокне, нижн - на хлопчатобумажной ткани.stains on polyacrylonitrile fiber, the bottom - on cotton fabric.
Claims (3)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU782640878A SU727664A1 (en) | 1978-07-07 | 1978-07-07 | Ammonium or sulfonium derivative of 2,9-dichloromethylquinacrydone possessing properties of cyanal and cationic dye |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU782640878A SU727664A1 (en) | 1978-07-07 | 1978-07-07 | Ammonium or sulfonium derivative of 2,9-dichloromethylquinacrydone possessing properties of cyanal and cationic dye |
Publications (1)
Publication Number | Publication Date |
---|---|
SU727664A1 true SU727664A1 (en) | 1980-04-15 |
Family
ID=20775427
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU782640878A SU727664A1 (en) | 1978-07-07 | 1978-07-07 | Ammonium or sulfonium derivative of 2,9-dichloromethylquinacrydone possessing properties of cyanal and cationic dye |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU727664A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5137576A (en) * | 1988-10-01 | 1992-08-11 | Hoechst Aktiengesellschaft | Quinacridones having selectively adjusted triboelectric effects |
US6264733B1 (en) * | 1999-02-02 | 2001-07-24 | Ciba Specialty Chemicals Corporation | Pigment particle growth and/or crystal phase directors |
CN104448896A (en) * | 2014-10-28 | 2015-03-25 | 江苏工程职业技术学院 | Preparation method of antibacterial azo dye for polyarmide fibers |
-
1978
- 1978-07-07 SU SU782640878A patent/SU727664A1/en active
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5137576A (en) * | 1988-10-01 | 1992-08-11 | Hoechst Aktiengesellschaft | Quinacridones having selectively adjusted triboelectric effects |
US6264733B1 (en) * | 1999-02-02 | 2001-07-24 | Ciba Specialty Chemicals Corporation | Pigment particle growth and/or crystal phase directors |
CN104448896A (en) * | 2014-10-28 | 2015-03-25 | 江苏工程职业技术学院 | Preparation method of antibacterial azo dye for polyarmide fibers |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS61245385A (en) | Dyeing of natural polyamide fiber material | |
AT335587B (en) | LAUNDRY, NETS AND COLOR SUPPLIES | |
SU727664A1 (en) | Ammonium or sulfonium derivative of 2,9-dichloromethylquinacrydone possessing properties of cyanal and cationic dye | |
CA1164159A (en) | Process for the finishing of fibrous materials | |
DE1965765A1 (en) | Process for washing freshly dyed textile material | |
EP0248356B1 (en) | Naphthalimides containing sulfuric-acid ester groups, process for their preparation and their use | |
SU740765A1 (en) | Dichloromethyltetrabenzoporphyrin ammonium or sulfonium derivatives possessing properties of cyanals and cationic dyes | |
EP0246551A2 (en) | Bis-benzoxazolylnaphthalenes containing sulfonate or sulfonamide groups, process for their preparation, and their use | |
EP0758005A1 (en) | Vat dyes mixtures, process to manufacture them and their use in dyeing cellulose-containing fibrous materials | |
SU1578161A1 (en) | Chlorous tetra(n-methyl-pyridinyl)octaphenyltetraazaporefin for dyeing polycrolonitrile or cellulose fibre | |
SU1028672A1 (en) | Ammonium or sulfoammonium derivatives of tetra(methyl-phenyl)prophine for dyeing polyacrylonitrile or cellulose fiber | |
DE4402210A1 (en) | Process for the production of aminated cotton fibers | |
EP0109029B1 (en) | Process for the dyeing of textile goods containing modified polyester fibres | |
DE2405152B2 (en) | Anthraquinone compounds containing sulfonic groups, their preparation and their use | |
SU303898A1 (en) | Method of dyeing textile materials and printing on them | |
SU1260377A1 (en) | Tetra-(para-methylthiosulfatphenyl)-porphin for dyeing wool,polyamide and cellulose fibres | |
US3835155A (en) | Blue disperse 1,4-diaminoanthraquinone-2,3-dicarboximide dyes | |
DE1644663C3 (en) | Anthraquinone reactive dyes, process for their preparation and their use | |
AT153974B (en) | Process for improving the fastness of dyeings with water-soluble dyes on fibers, fabrics and the like. like | |
DE2365762B2 (en) | Anthraquinone dyes, their manufacture and use | |
DE2341427C3 (en) | Method of making multicolor effects n | |
SU383322A1 (en) | ||
US3461141A (en) | 1-amino-4-cyclopentadienylamino-2-anthraquinone sulfonic acids | |
DE3830686A1 (en) | THERMOFIXING METHOD FOR ALKALIFREE CREATION AND PRINTING WITH REACTIVE POWERS AND WATER-SOLUBLE SULFUR Paints | |
DE2254498C3 (en) | Process for dyeing fiber material |