GB941009A - Dyes containing hydrazino groups - Google Patents

Dyes containing hydrazino groups

Info

Publication number
GB941009A
GB941009A GB578162A GB578162A GB941009A GB 941009 A GB941009 A GB 941009A GB 578162 A GB578162 A GB 578162A GB 578162 A GB578162 A GB 578162A GB 941009 A GB941009 A GB 941009A
Authority
GB
United Kingdom
Prior art keywords
sulphonic acid
hydrazine
reacting
dye
aminoethyl
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
GB578162A
Inventor
Arnold Tartter
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.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik 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 BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB941009A publication Critical patent/GB941009A/en
Expired legal-status Critical Current

Links

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
    • C09B69/00Dyes not provided for by a single group of this subclass
    • 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
    • C09B43/00Preparation of azo dyes from other azo compounds
    • C09B43/40Preparation of azo dyes from other azo compounds by substituting hetero atoms by radicals containing other hetero atoms
    • 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
    • C09B47/00Porphines; Azaporphines
    • C09B47/04Phthalocyanines abbreviation: Pc
    • C09B47/08Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
    • C09B47/24Obtaining compounds having —COOH or —SO3H radicals, or derivatives thereof, directly bound to the phthalocyanine radical
    • C09B47/26Amide radicals
    • 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
    • C09B62/00Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/44Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
    • C09B62/523Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an esterified or non-esterified hydroxyalkyl sulfonyl amido or hydroxyalkyl amino sulfonyl group, a quaternised or non-quaternised amino alkyl sulfonyl amido group, or a substituted alkyl amino sulfonyl group, or a halogen alkyl sulfonyl amido or halogen alkyl amino sulfonyl group or a vinyl sulfonylamido or a substituted vinyl sulfonamido group
    • 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
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/0056Dyeing with polymeric dyes involving building the polymeric dyes on the fibres
    • D06P1/0064Dyeing with polymeric dyes involving building the polymeric dyes on the fibres by using reactive polyfunctional compounds, e.g. crosslinkers
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Structural Engineering (AREA)
  • Coloring (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

In examples, (6), N-b -(11-acetylaminonaphthalene - 51- sulphonylamino) ethyl - N1 - isopropylidene-hydrazine is made by reacting 1-acetylamino naphthalene - 5 - sulphonic acid chloride with N-b -aminoethyl-N1- isopropyl-idene-hydrazine; (9), N-b -aminoethyl-N-phenyl-hydrazine is made by reacting phenylhydrazine with chloroethylamine hydrochloride, neutralising and fractioning the product; and (10) N-b -aminoethyl-N1-isopropylidene-hydrazine is made by reacting acetone with b -aminoethyl hydrazine.ALSO:The invention comprises dyes of the azo, anthraquinone and tetrazaporphin series containing at least one group of the formula <FORM:0941009/C3/1> where R is hydrogen, substituted or unsubstituted alkyl, cycloalkyl, aryl or aralkyl, A is alkylene with two to six carbon atoms in the alkylene chain and X is a hydrazino group containing at least one free hydrogen atom. The dyes are made by reacting a sulphonic acid halide of a dye or of a dye precursor of the aminobenzene sulphonic acid or aminonaphthalene sulphonic acid series with an amine of the formula: R-NH-A-X, in which the hydrazine group may be protected by an acyl or alkylidene group, in a solvent or diluent at about 0 DEG to 90 DEG C., or by reacting a sulphonic acid alkylene imide or a mineral acid ester of a sulphonic acid hydroxy-alkylamide of a dye or a dye precursor of the aminobenzene, sulphonic acid or aminonaphthalene sulphonic acid series with a hydrazine having at least two free hydrogen atoms and, when a precursor is used, reacting the product with a dyestuff sulphonic acid halide or coupling it with a diazotized amine. Examples are given. The dyes may be converted into the corresponding methylol or methylol ether derivatives. They dye natural or regenerated textile materials.
GB578162A 1961-02-16 1962-02-15 Dyes containing hydrazino groups Expired GB941009A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB61291A DE1207526B (en) 1961-02-16 1961-02-16 Process for the preparation of dyes containing hydrazino groups

Publications (1)

Publication Number Publication Date
GB941009A true GB941009A (en) 1963-11-06

Family

ID=6973146

Family Applications (1)

Application Number Title Priority Date Filing Date
GB578162A Expired GB941009A (en) 1961-02-16 1962-02-15 Dyes containing hydrazino groups

Country Status (4)

Country Link
BE (1) BE613989A (en)
CH (2) CH422192A (en)
DE (1) DE1207526B (en)
GB (1) GB941009A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002070609A1 (en) * 2001-03-03 2002-09-12 Avecia Limited Ink jet printing composition comprising a dye containing hydrazine or hydrazide
US7141106B2 (en) 2001-03-03 2006-11-28 Fujifilm Imaging Colorants Limited Ink jet printing composition comprising a dye containing hydrazine or hydrazide

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1066987B (en) * 1959-10-15 Ciba Aktiengesellschaft, Basel (Schweiz) Process for dyeing or printing cellulosic materials with a fibrous structure
FR1254330A (en) * 1959-04-17 1961-02-17 Sandoz Ag Reactive dyes bearing a halo-alkyl group, their production process and their applications

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002070609A1 (en) * 2001-03-03 2002-09-12 Avecia Limited Ink jet printing composition comprising a dye containing hydrazine or hydrazide
GB2389588A (en) * 2001-03-03 2003-12-17 Avecia Ltd Ink jet printing composition comprising a dye containing hydrazine or hydrazide
GB2389588B (en) * 2001-03-03 2005-03-23 Avecia Ltd Ink jet printing composition comprising a dye containing hydrazide groups
US7141106B2 (en) 2001-03-03 2006-11-28 Fujifilm Imaging Colorants Limited Ink jet printing composition comprising a dye containing hydrazine or hydrazide

Also Published As

Publication number Publication date
BE613989A (en) 1962-08-16
CH422192A (en) 1966-10-15
DE1207526B (en) 1965-12-23
CH420429A (en) 1966-09-15

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