GB400870A - Manufacture of dyestuffs - Google Patents

Manufacture of dyestuffs

Info

Publication number
GB400870A
GB400870A GB13601/33A GB1360133A GB400870A GB 400870 A GB400870 A GB 400870A GB 13601/33 A GB13601/33 A GB 13601/33A GB 1360133 A GB1360133 A GB 1360133A GB 400870 A GB400870 A GB 400870A
Authority
GB
United Kingdom
Prior art keywords
sulpho
methoxy
aminodiphenylamine
condensed
dinitrobenzoic
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
GB13601/33A
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
Publication of GB400870A publication Critical patent/GB400870A/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
    • C09B51/00Nitro or nitroso dyes

Landscapes

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

Abstract

p-Aminodiphenylamine or its homologues or substitution products are condensed with 2-alkoxy-3 : 5-dinitro- or 4-alkoxy-3 : 5- dinitrobenzoic acids or alkyl esters to give dyes which yield yellow-brown to red-brown fast shades on animal fibres. Condensation may be conducted in a suitable solvent or diluent with or without the addition of an acid-binding agent such as sodium acetate, sodium carbonate, calcium carbonate, magnesium oxide. In examples: (1) 4-aminodiphenylamine-2-sulphonic acid is condensed with 4- and 2-methoxy-3 : 5-dinitrobenzoic acids (prepared by nitrating p- and o-methoxybenzoic acids); (2) 4-amino-diphenylamine is condensed with the methyl or ethyl ester of 4-methoxy-3 : 5-dinitrobenzoic acid. The use of the following derivatives of 4-aminodiphenylamine is also specified: 2 - sulpho - 4<1> - methyl, 2 - sulpho - 2<1> - carboxy, 2-carboxy, 2-sulpho-4<1>-methoxy-, 2-sulpho-2<1>-methoxy, 2-sulpho-4<1>-hydroxy-, and 4<1>-sulpho. Specification 279,133, [Class 2 (iii), Dyes &c.], is referred to.
GB13601/33A 1932-05-10 1933-05-10 Manufacture of dyestuffs Expired GB400870A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE400870X 1932-05-10

Publications (1)

Publication Number Publication Date
GB400870A true GB400870A (en) 1933-11-02

Family

ID=6402508

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13601/33A Expired GB400870A (en) 1932-05-10 1933-05-10 Manufacture of dyestuffs

Country Status (1)

Country Link
GB (1) GB400870A (en)

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