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 PDF

Info

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
Application number
SU782640878A
Other languages
Russian (ru)
Inventor
Роза Андреевна Петрова
Тамара Ильинична Потапова
Ольга Дмитриевна Краева
Original Assignee
Ивановский Химико-Технологический Институт
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 Ивановский Химико-Технологический Институт filed Critical Ивановский Химико-Технологический Институт
Priority to SU782640878A priority Critical patent/SU727664A1/en
Application granted granted Critical
Publication of SU727664A1 publication Critical patent/SU727664A1/en

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)

Формула изобретени Invention Formula Аммониевое или сульфониевое производное 2,9-дихлорметилхинакридона формулыAmmonium or sulfonium derivative of 2,9-dichloromethylquinacridone formula 5/55/5 5/5.5/5. 5/55/5 5/45/4 5/55/5 5/45/4 5/55/5 5/55/5 (jHjTJ U I или ыССН) 1 5 J «f,,.4 n v ujJiJ про вл ющее свойство цианала и катионного красител .. 72766 46 Источники информации, прин тые во внимание при экспертизе 1.Проспект по катионным красител м . Хими  , i НИОПИК, М., 1971, (jHjTJ U I or syCN) 1 5 J "f ,,. 4 n v ujJiJ showing the property of cyanal and cationic dye .. 72766 46 Information sources taken into account during the examination 1. Prospect of cationic dyes. Chemistry, i NIOPIK, M., 1971, 2.Андросов В.Ф., Голомб Л.М. Синтетические красители в текстильной промышленности. Легка  индуст и - , М., с. 156, 1963. 2. Androsov V.F., Golomb L.M. Synthetic dyes in the textile industry. Light industrial and - M., p. 156, 1963. 3. :Органические синтетические красители. Каталог, НИОПИК, М., 1977.3.: Organic synthetic dyes. Catalog, NIOPIK, M., 1977.
SU782640878A 1978-07-07 1978-07-07 Ammonium or sulfonium derivative of 2,9-dichloromethylquinacrydone possessing properties of cyanal and cationic dye SU727664A1 (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (3)

* Cited by examiner, † Cited by third party
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
CH427572A (en) Process for the production of an ammunition body and ammunition body produced by this process
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