GB1402061A - Disazo pigmetn - Google Patents

Disazo pigmetn

Info

Publication number
GB1402061A
GB1402061A GB4141073A GB4141073A GB1402061A GB 1402061 A GB1402061 A GB 1402061A GB 4141073 A GB4141073 A GB 4141073A GB 4141073 A GB4141073 A GB 4141073A GB 1402061 A GB1402061 A GB 1402061A
Authority
GB
United Kingdom
Prior art keywords
pigment
tio
give
dioctylphthalate
sept
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
GB4141073A
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 GB1402061A publication Critical patent/GB1402061A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • 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
    • 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
    • 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
    • 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
    • C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0025—Crystal modifications; Special X-ray patterns
    • C09B67/0028—Crystal modifications; Special X-ray patterns of azo compounds

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)
  • Inks, Pencil-Leads, Or Crayons (AREA)
  • Paints Or Removers (AREA)
  • Crystals, And After-Treatments Of Crystals (AREA)

Abstract

1402061 Coloured polymer compositions CIBA-GEIGY AG 4 Sept 1973 [5 Sept 1972] 41410/73 Headings C3P and C3R [Also in Division C4] The disazo pigment is claimed in its #- and Y-modifications. The pigments may be used to colour high molecular weight material in the form of plastics, melts, spinning solutions, lacquers or printing inks. Such materials include cellulose ethers and esters, aminoplasts, alkyd resins, phenolic plastics, polycarbonates, polyolefines, polyacrylonitrile, polyacrylic acid esters, polyamides, polyurethanes, polyesters, rubber, casein and silicones. Polyvinyl chloride, dioctylphthalate and the pigment are roll milled at 140‹ C. to give yellowish red sheet; polyvinylchloride suspension, a stabilizer, the pigment, and TiO 2 are roll mixed at 180‹ C. and pressed to give red p.v.c. board; p.v.c. emulsion, dioctylphthalate, epoxidized soya oil, TiO 2 , and the pigment are processed at 160‹ C. to give p.v.c. sheet. Alkydmelamine stoving varnish, TiO 2 and the pigment produce a brilliant red lacquer which may be coated on aluminium. Similarly coconut alkyd resin, melamine resin, xylene, ethylene glycol monomethyl ether, TiO 2 , and the pigment may be sprayed on to aluminium and stoved at 120‹ C.
GB4141073A 1972-09-05 1973-09-04 Disazo pigmetn Expired GB1402061A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH1303472A CH579128A5 (en) 1972-09-05 1972-09-05

Publications (1)

Publication Number Publication Date
GB1402061A true GB1402061A (en) 1975-08-06

Family

ID=4388697

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4141073A Expired GB1402061A (en) 1972-09-05 1973-09-04 Disazo pigmetn

Country Status (16)

Country Link
JP (1) JPS4967920A (en)
AR (1) AR199683A1 (en)
AU (1) AU469450B2 (en)
BE (1) BE804483A (en)
BR (1) BR7306748D0 (en)
CA (1) CA1001156A (en)
CH (1) CH579128A5 (en)
CS (1) CS177142B2 (en)
DE (1) DE2344313A1 (en)
DK (1) DK133112C (en)
ES (1) ES418462A1 (en)
FR (1) FR2197945B1 (en)
GB (1) GB1402061A (en)
IT (1) IT995279B (en)
NL (1) NL7312079A (en)
SU (1) SU667149A3 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH629529A5 (en) * 1977-11-04 1982-04-30 Ciba Geigy Ag NEW MODIFICATION OF A DISAZOPIGMENT.

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH460991A (en) * 1965-08-19 1968-08-15 Geigy Ag J R Process for the production of a disazo pigment
CH477522A (en) * 1966-07-15 1969-08-31 Geigy Ag J R Process for the production of a disazo pigment

Also Published As

Publication number Publication date
JPS4967920A (en) 1974-07-02
DK133112C (en) 1976-09-06
IT995279B (en) 1975-11-10
FR2197945A1 (en) 1974-03-29
AU469450B2 (en) 1976-02-12
BE804483A (en) 1974-03-05
CH579128A5 (en) 1976-08-31
DE2344313A1 (en) 1974-03-21
NL7312079A (en) 1974-03-07
DK133112B (en) 1976-03-22
SU667149A3 (en) 1979-08-05
ES418462A1 (en) 1976-07-16
BR7306748D0 (en) 1974-07-18
AR199683A1 (en) 1974-09-23
CA1001156A (en) 1976-12-07
CS177142B2 (en) 1977-07-29
AU5966473A (en) 1975-02-27
FR2197945B1 (en) 1976-10-01

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee