ES305155A1 - New disazo pigments and processes for their manufacture - Google Patents

New disazo pigments and processes for their manufacture

Info

Publication number
ES305155A1
ES305155A1 ES0305155A ES305155A ES305155A1 ES 305155 A1 ES305155 A1 ES 305155A1 ES 0305155 A ES0305155 A ES 0305155A ES 305155 A ES305155 A ES 305155A ES 305155 A1 ES305155 A1 ES 305155A1
Authority
ES
Spain
Prior art keywords
formula
halogen atom
alkoxy
hydrogen
alkyl
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
ES0305155A
Other languages
Spanish (es)
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.)
Novartis AG
Original Assignee
Ciba Geigy 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 Ciba Geigy AG filed Critical Ciba Geigy AG
Publication of ES305155A1 publication Critical patent/ES305155A1/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/22—Compounds containing nitrogen bound to another nitrogen atom
    • C08K5/23—Azo-compounds
    • C08K5/235—Diazo and polyazo compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/32—Compounds containing nitrogen bound to oxygen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • 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
    • C09B33/00—Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
    • C09B33/02—Disazo dyes
    • C09B33/147—Disazo dyes in which the coupling component is a bis -(-o-hydroxy-carboxylic- acid amide)
    • 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
    • C09B41/00—Special methods of performing the coupling reaction
    • C09B41/006—Special methods of performing the coupling reaction characterised by process features
    • C09B41/008—Special methods of performing the coupling reaction characterised by process features using mechanical or physical means, e.g. using ultra-sound, milling during coupling or microreactors
    • 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
    • C09B43/00—Preparation of azo dyes from other azo compounds
    • C09B43/32—Preparation of azo dyes from other azo compounds by reacting carboxylic or sulfonic groups, or derivatives thereof, with amines; by reacting keto-groups with amines
    • C09B43/38—Preparation of azo dyes from other azo compounds by reacting carboxylic or sulfonic groups, or derivatives thereof, with amines; by reacting keto-groups with amines by reacting two or more ortho-hydroxy naphthoic acid dyes with polyamines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Photoreceptors In Electrophotography (AREA)

Abstract

Disazo pigments of general formula <FORM:1037988/C4-C5/1> in which Hal is halogen, either both X's are hydrogen atoms or alkyl or alkoxy groups or one X is a hydrogen atom the other being a halogen atom or an alkyl, alkoxy, cyano or trifluoromethyl group and Z is a hydrogen or halogen atom or an alkoxy group, are prepared by reacting an acid chloride of formula <R/2> with a diamine of formula <FORM:1037988/C4-C5/2> or by coupling a diazotized 2-nitro-4-halogenoaniline with a compound of formula <FORM:1037988/C4-C5/3> or with a compound of formula <FORM:1037988/C4-C5/4> The -CH2A in which A is an amine group is split off and replaced by the diazo compound. The preferred compounds are those in which the halogen is chlorine and both X's are methyl groups. The pigments give brown colours.ALSO:Disazo pigments of general formula <FORM:1037988/C3/1> in which Hal is a halogen atom, both X's represent hydrogen atoms or alkyl or alkoxy groups or one X is hydrogen and the other X is a halogen atom or an alkyl, alkoxy, cyano or trifluoromethyl group and 2 is a hydrogen or halogen atom or an alkoxy group, are incorporated into, polyvinyl chloride-dioctylphthalate mixture (Example 4) an alkyd melaminetitanium dioxide stoving lacquer (Example 5), and into a nitrocellulose-titanium dioxide lacquer (Example 6), or into various other resins mentioned generally.
ES0305155A 1963-10-22 1964-10-21 New disazo pigments and processes for their manufacture Expired ES305155A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH1295363A CH434520A (en) 1963-10-22 1963-10-22 Process for the production of new disazo pigments

Publications (1)

Publication Number Publication Date
ES305155A1 true ES305155A1 (en) 1965-04-01

Family

ID=4387933

Family Applications (2)

Application Number Title Priority Date Filing Date
ES0305155A Expired ES305155A1 (en) 1963-10-22 1964-10-21 New disazo pigments and processes for their manufacture
ES0305154A Expired ES305154A1 (en) 1963-10-22 1964-10-21 New disazo pigments and processes for their manufacture

Family Applications After (1)

Application Number Title Priority Date Filing Date
ES0305154A Expired ES305154A1 (en) 1963-10-22 1964-10-21 New disazo pigments and processes for their manufacture

Country Status (6)

Country Link
BE (2) BE654649A (en)
CH (1) CH434520A (en)
DE (2) DE1544428C3 (en)
ES (2) ES305155A1 (en)
GB (2) GB1058749A (en)
NL (2) NL6412256A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4046755A (en) * 1971-12-13 1977-09-06 Ciba-Geigy Corporation Disazo pigments containing naphthalene coupling components
NL7316786A (en) * 1972-12-12 1974-06-14
US4127567A (en) * 1972-12-12 1978-11-28 Sandoz Ltd. Bis-(1-substituted phenylazo-2-hydroxynaphthalene-3-carboxamido)naphthalenes
CH584744A5 (en) * 1973-12-20 1977-02-15 Ciba Geigy Ag

Also Published As

Publication number Publication date
GB1037988A (en) 1966-08-03
BE654650A (en) 1965-04-21
ES305154A1 (en) 1965-05-01
DE1544428A1 (en) 1970-04-16
GB1058749A (en) 1967-02-15
DE1544429A1 (en) 1970-04-16
NL6412256A (en) 1965-04-23
CH434520A (en) 1967-04-30
NL6412255A (en) 1965-04-23
DE1544428B2 (en) 1973-09-06
DE1544428C3 (en) 1974-04-11
BE654649A (en) 1965-04-21

Similar Documents

Publication Publication Date Title
ES305155A1 (en) New disazo pigments and processes for their manufacture
GB1016515A (en) Basic monoazo dyes and their production
GB1005899A (en) Diazotype copying material, and diazonium salts suitable for use therein
GB1142309A (en) Improved urea derivatives and their use as herbicides
GB1352100A (en)
GB1285238A (en) Disazo dyes
GB1095232A (en) Process for the production of azo compounds
GB1104537A (en) 3-pyrazolyl-7-aryltriazolyl-coumarins and process for the preparation thereof
GB1052002A (en)
GB1338250A (en) Basic azo dyes their production and use
ES387858A1 (en) Sparingly soluble disazo compounds their production and use as pigments
GB1053490A (en)
ES322224A1 (en) Processes for the manufacture of disazo pigments
ES414836A2 (en) Water-insoluble monoazo dyestuffs
GB1348591A (en) Disazo dyestuffs a process for their manufacture and their use
GB1028564A (en) Water-insoluble monoazo-dyestuffs and process for their manufacture
ES427401A1 (en) Disazo pigments and a process for their manufacture
GB1070765A (en) Monoazo pigments derived from hydroxynaphthoic acid amide derivatives and processes for their manufacture and use
GB1003448A (en) New water-insoluble monoazo-dyestuffs
GB1019113A (en) Improvements relating to water-soluble quaternised colour salts of triazene compounds and their use
ES385420A1 (en) Substituted 4-(2-nitroisobutylamino)-azobenzene
ES381812A1 (en) Compounds of the azobenzene series their production and use as disperse dyes
GB1405775A (en) Naphtholic acid amide colour couplers and their use in colour photography
GB1088611A (en) Monoazo basic dyes their production and use
GB1352464A (en) N-alkyl-alpha-3,5-substituted phenoxy-alkyl amides and their use as herbicides