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DE475553C - Process for the production of real colors on the vegetable fiber - Google Patents

Process for the production of real colors on the vegetable fiber

Info

Publication number
DE475553C
DE475553C DEC36744D DEC0036744D DE475553C DE 475553 C DE475553 C DE 475553C DE C36744 D DEC36744 D DE C36744D DE C0036744 D DEC0036744 D DE C0036744D DE 475553 C DE475553 C DE 475553C
Authority
DE
Germany
Prior art keywords
amino
aryl
alkyl
vegetable fiber
production
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
Application number
DEC36744D
Other languages
German (de)
Inventor
Dr Arthur Zitscher
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to DEC36744D priority Critical patent/DE475553C/en
Application granted granted Critical
Publication of DE475553C publication Critical patent/DE475553C/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/10Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
    • C09B29/18Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides
    • C09B29/20Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides of the naphthalene series
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/58Material containing hydroxyl groups
    • D06P3/60Natural or regenerated cellulose
    • D06P3/68Preparing azo dyes on the material

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Description

Verfahren zur Erzeugung echter Färbungen auf der pflanzlichen Faser In dem Patent 467 545 ist ein Verfahren zur Erzeugung echter Färbungen auf der pflanzlichen Faser beschrieben, welches darin besteht, daß man die mit 2 - 3-Oxynaphthoesäure-J3-nap,hthaäd imprägnierte Faser mit den Diazoverbindungen solcher Aminobasen. behandelt, welche in ?- - 5-SteHung zur Amino-,gruppe Substituenten tragen, von denen mindestens einer ein Chloratom, ist. Die erhaltenen Färbungen zeichnen sich neben andeeren Echtheitseigenschaften besonders durch ihre gute Beur-hbeständigkeit aus.A method for generating real dyeings on the plant fiber in the patent 467 545 a method for generating real dyes is described on vegetable fiber, which consists in that the 2 - 3-oxynaphthoic acid-J3-nap, hthaäd impregnated fiber with the Diazo compounds of such amino bases. treated, which in ? - - 5-position to the amino, group carry substituents, of which at least one is a chlorine atom. In addition to other fastness properties, the dyeings obtained are particularly notable for their good resistance to testing.

Bei der weiteren Bearbeitung dieses Erfindungsgedankens wurde nun gefunden, daß man zu neuen, gleich wertvollen Färbungen gelangt, wenn man in dem Verfahren solche in 2 - 5-Stellung zur Aminogruppe- substituierten Basen verwendet, welche an Stelle eines Chloratoms eine der Gruppen - SO. - R oder - CO - R tragen-, worin R einen Alkyl, Aryl- bzw. Aralk-ylrest oder einem Alkyl, Aryl- bzw. Aralk,ylamidrest bedeutet, also Derivate von aromatischen Ketonen, Sulfonen, S"ulfosäu#r-e- und Carbonsäureary.U,den. Dabei so-Ilen die Alkyl-, Aryl- und Aralkylamide der Alkyloxy-, Aryloxy- und Aralkyloxy-m-aminoben7,oesäure ausgenommen sein. An zweiter Stelle kommen beliebige Substituenten in Betracht, wie z. B. Alkyl-, Alkyloxy-, Aryloxy- und Aralkyloxygruppen, Halogene u. dgl. - Man erhält so Farbstoffe, welche neben einer klaren Nuance eine besonders gute Beuchechtheit aufweisen.In the further processing of this inventive idea has now been found that leads to new, equally valuable dyes when such in the method in 2 - 5 positions are used to Aminogruppe- substituted bases which instead of a chlorine atom one of the groups - SO. - R or - CO - R carry, in which R denotes an alkyl, aryl or aralkyl radical or an alkyl, aryl or aralkylamide radical, that is to say derivatives of aromatic ketones, sulfones, sulfonates and Carboxylic acid ary.U, the alkyl, aryl and aralkyl amides of the alkyloxy, aryloxy and aralkyloxy-m-aminobes7, oesäure be excluded -, alkyloxy, aryloxy and aralkyloxy groups, halogens and the like - This gives dyes which, in addition to a clear shade, have particularly good color fastness.

Beispiel Gut ausgekochtes und getrocknetes Garn wird mit einer Lösung von 3 g 2 - 3-OxY-naplithoesä-ur,e-13-napht'halid, 9 ccm NatronlaUge 34' B6 und 8 ccm Türkis,chrotöl im Liter imprägniert, gründlich abgewunden und, ohne zu trocknen, in einer mit Kreide neutralisierten Diazolösung, welche 4,9 9 -2-AminotO1Y1-4-phenylsulfon,oder 4,79 4-Chlor-3-aininobenzan-ilid im Liter enthält, entwickelt, gezspült und geseift.Good example of boiled and dried yarn is treated with a solution of 3 g of 2 - 3-oxy-naplithoesä-ur e-napht'halid 13, 9 cc of sodium hydroxide solution 34 'B6 and 8 cc turquoise, chrotöl impregnated in liters, thoroughly unwound and Without drying, developed, rinsed and soaped in a diazo solution neutralized with chalk, which contains 4,9 9 -2-aminotO1Y1-4-phenylsulfone, or 4,79 4-chloro-3-aininobenzanilide per liter.

Miari erhält SO Mit 2-AmincktO1Y1-4-phenylsulfon eine blaustichi g-, mit 4-Chlor-3-2nlinobenzanilid eine gelbstichigrote Färbung von sehr guter Beuchechtheit.Miari obtained by using the 2-phenyl sulfone AmincktO1Y1-4 a blaustichi g-, with 4-chloro-3-2nlinobenzanilid a gelbstichigrote coloring of very good Beuchechtheit.

Die neuen Farbstoffe können auch im Druckverfahren nach einer der üblichen Arbeitsweisen erzeugt werden.The new dyes can also be used in the printing process according to one of the usual working methods.

In der nachfolgenden Tabelle sind die Nuancen einer Anzahl nach dem vorliegenden Verfahren hergestellter Färbungen zusammengestellt: -- 2 -3-Oxvnaphthol-g-naphthylamin, gelzuppelt mit der I 'Dia:zo- bzw. Tetrazoverbindung aus Nuance 3-Anüno-4-phenoxy-benzophenon bordo 3'Amino-4'-methyl-benzoyl-2-chloranilin lebhaftes Scharlach 3'Amino-4'-methyl-benzoyl-2-anisidin lebhaftes Scharlachrot 3'-Amino-4'-methyl-benzoyl-2-aininodiphenyläther klares Scharlachrot 3'-Amin0-4'#methyl-benzOYI-3-toluidin lebhaftes Scharlach 3'Amino-4'-methyl-benzoyl-4-phenetidin 3'-Amin0-4'-methyl-benzoyl-4-chlor-,-,-toluidin klares Rot 3'-Amino-4'-methyl-benzOYI-5-chlor-2-anisidin klares Scharlachrot 3 - 3-Diamino-4 - 4'-ditO1Y1ketOn leuchtendes Scharlach Bis-(3'-amino-4'-methyl-benzoyl)-dianisidin kupferrot Bis-(3'-amino-4'-methyl-benzoyl)-o-tolidin korinth 3-Arnino-4-chlor-diphenylsuffon rot 2,-Amino-tolyl-4-benzylsulfon klares Scharlachrot 2-Amino-toluol-4-sulfodünethylamid leuchtendes Scharlach 2-Amino-phenetol-4-sulfodirnethylamid blaustichigrot In the following table the nuances of a number produced by the present process dyeings are summarized: - 2 -3-Oxvnaphthol-g-naphthylamine, gelled with the I 'Dia: zo- or tetrazo compound from Nuance 3-Anüno-4-phenoxy-benzophenone bordo 3'Amino-4'-methyl-benzoyl-2-chloroaniline vivid scarlet fever 3'Amino-4'-methyl-benzoyl-2-anisidine bright scarlet 3'-Amino-4'-methyl-benzoyl-2-ainodiphenyl ether clear scarlet red 3'-Amin0-4 '# methyl-benzOYI-3-toluidine vivid scarlet fever 3'Amino-4'-methyl-benzoyl-4-phenetidine 3'-Amin0-4'-methyl-benzoyl-4-chloro -, -, - toluidine clear red 3'-Amino-4'-methyl-benzOYI-5-chloro-2-anisidine clear scarlet red 3 - 3-Diamino-4 - 4'-ditO1Y1ketOn bright scarlet Bis- (3'-amino-4'-methyl-benzoyl) -dianisidine copper red Bis- (3'-amino-4'-methyl-benzoyl) -o-tolidine corinth 3-Amino-4-chloro-diphenylsuffon red 2, -amino-tolyl-4-benzylsulfone clear scarlet red 2-Amino-toluene-4-sulfodünethylamide bright scarlet fever 2-Amino-phenetol-4-sulfodimethylamide bluish-tinted red

Claims (1)

PATEN TA NS PRUCH: Abänderung des durch das Hauptpatent 467 545 geschützten Verfahrens zur Erzeugung echter Färbungen auf der pflanzlichen Faser, darin bestehend, daß man an Stelle der Diazoverbindungen solcher Aminobasen, welche in 2 - 5 -Stellung zur Aminogruppe Substituenten tragen, von denen mindestens einerein Chloratom ist, hier die Diazoverbindungen von 2 - 5-substituierten Aminobasen, welche an Stelle eines Chloratoms eine der Gruppen -SO.-R oder -CO-R enflialten, worin R einen Alkyl-, Aryl-bzw. Aralkylrest oder einen Alkyl-, Aryl-bzw. AraJkylaminrest bedeutet, auf die mit -- - 3-Oxynaphthoesäure-p-naphthahd unprägnierte Faser einwirken läßt, wobei die Ver,vendung von Alkyl-, Aryl- und Aralkylamiden der Alkyloxy, Aryloxy- und Aralkyloxy-m-aniinobenzoesäur-e ausgenommen sein soll.PAT EN TA NS Pruch: modification of protected by the main patent 467,545 a process for forming a true dyeings on the vegetable fiber, consisting in that in place of diazo compounds such amino bases, which in 2 - 5 - wear to the amino substituents, of which at least one pure chlorine atom, here, the diazo compounds 2-5-substituted amino bases which enflialten instead of a chlorine atom one of the groups -SO.-R or -CO-R, wherein R is an alkyl or aryl. Aralkyl radical or an alkyl, aryl or. AraJkylaminrest means, on which - - 3-oxynaphthoic acid-p-naphthahd impregnated fiber is allowed to act, the use of alkyl, aryl and aralkylamides of alkyloxy, aryloxy and aralkyloxy-m-aniinobenzoic acid to be excluded .
DEC36744D 1925-05-29 1925-05-29 Process for the production of real colors on the vegetable fiber Expired DE475553C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEC36744D DE475553C (en) 1925-05-29 1925-05-29 Process for the production of real colors on the vegetable fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEC36744D DE475553C (en) 1925-05-29 1925-05-29 Process for the production of real colors on the vegetable fiber

Publications (1)

Publication Number Publication Date
DE475553C true DE475553C (en) 1929-04-27

Family

ID=7022430

Family Applications (1)

Application Number Title Priority Date Filing Date
DEC36744D Expired DE475553C (en) 1925-05-29 1925-05-29 Process for the production of real colors on the vegetable fiber

Country Status (1)

Country Link
DE (1) DE475553C (en)

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