GB914453A - Dyes of the anthraquinone series - Google Patents

Dyes of the anthraquinone series

Info

Publication number
GB914453A
GB914453A GB2935560A GB2935560A GB914453A GB 914453 A GB914453 A GB 914453A GB 2935560 A GB2935560 A GB 2935560A GB 2935560 A GB2935560 A GB 2935560A GB 914453 A GB914453 A GB 914453A
Authority
GB
United Kingdom
Prior art keywords
group
anthraquinone
dyes
formula
nucleus
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
GB2935560A
Inventor
Willy Braun
Ernst Hartwig
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 GB914453A publication Critical patent/GB914453A/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
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/50—Amino-hydroxy-anthraquinones; Ethers and esters thereof
    • 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
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16—Amino-anthraquinones
    • C09B1/20—Preparation from starting materials already containing the anthracene nucleus
    • C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
    • C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
    • 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
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16—Amino-anthraquinones
    • C09B1/20—Preparation from starting materials already containing the anthracene nucleus
    • C09B1/36—Dyes with acylated amino groups
    • C09B1/42—Dyes with acylated amino groups the acyl groups being residues of an aromatic carboxylic acid

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Polysryrene or linear polyamides, possibly with the addition of titanium dioxide are dyed in bulk with a dye of the anthraquinone series containing at least one para-(arylcarbonyl)-phenylamino radical attached to the nucleus. For dyeing polystyrene, dyes are preferred of the formula <FORM:0914453/IV(a)/1> where D is a group of the formula <FORM:0914453/IV(a)/2> and each of X1, Y1 and Z1 is hydrogen, a group D or a group of the formula <FORM:0914453/IV(a)/3> Red, violet and blue dyeings are obtained.ALSO:The invention comprises anthraquinone dyes containing at least one phenylaryl ketone radical, free from carboxylic acid groups, attached to the anthraquinone nucleus via an amino group in the position of the phenyl ring para to the keto group, and a process for making them by reacting at elevated temperatures an anthraquinone derivative containing at least one primary or secondary amino group directly attached to the nucleus with a p-halo-phenyl aryl ketone. Anthraquinone derivatives include aminophthaloylacridones, aminoanthrapyrimidines and amino-anthraquinones substituted by hydroxy, methoxy, acylamino, bromo and nitro groups. Aryl radicals may be substituted by hydroxy, alkyl or alkoxy but those specified are naphthyl, diphenyl and phenyl. Examples are given. The dyes are pigments for cellulose acetate, viscose, polyacrylonitrile, copolymers of acrylonitrile and polystyrene, giving red, violet and blue shades (see Group IV(a)).
GB2935560A 1959-08-28 1960-08-25 Dyes of the anthraquinone series Expired GB914453A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB54591A DE1128066B (en) 1959-08-28 1959-08-28 Process for the preparation of dyes of the anthraquinone series

Publications (1)

Publication Number Publication Date
GB914453A true GB914453A (en) 1963-01-02

Family

ID=6970664

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2935560A Expired GB914453A (en) 1959-08-28 1960-08-25 Dyes of the anthraquinone series

Country Status (4)

Country Link
BE (1) BE594368A (en)
CH (1) CH391930A (en)
DE (1) DE1128066B (en)
GB (1) GB914453A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6884899B2 (en) * 2001-08-16 2005-04-26 Bayer Aktiengesellschaft Preparation of 1-amino-4-hydroxyanthraquinones

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1284540B (en) * 1965-02-04 1968-12-05 Basf Ag Process for the preparation of anthraquinone dyes
US3507606A (en) * 1966-09-27 1970-04-21 Toms River Chemical Corp Acylphenylaminoanthraquinone dyes for linear polyester materials

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR828581A (en) * 1936-11-04 1938-05-20 Ig Farbenindustrie Ag Process for preparing compounds of the anthraquinone series

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6884899B2 (en) * 2001-08-16 2005-04-26 Bayer Aktiengesellschaft Preparation of 1-amino-4-hydroxyanthraquinones

Also Published As

Publication number Publication date
CH391930A (en) 1965-05-15
DE1128066B (en) 1962-04-19
BE594368A (en) 1961-02-24

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