GB342807A - The manufacture of acid disazodyestuffs - Google Patents

The manufacture of acid disazodyestuffs

Info

Publication number
GB342807A
GB342807A GB3534529A GB3534529A GB342807A GB 342807 A GB342807 A GB 342807A GB 3534529 A GB3534529 A GB 3534529A GB 3534529 A GB3534529 A GB 3534529A GB 342807 A GB342807 A GB 342807A
Authority
GB
United Kingdom
Prior art keywords
dyestuff
acid
give
dihydroxynaphthalene
diaminodiphenylmethane
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
GB3534529A
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
Priority to GB3534529A priority Critical patent/GB342807A/en
Publication of GB342807A publication Critical patent/GB342807A/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
    • C09B35/00Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • C09B35/02Disazo dyes
    • C09B35/039Disazo dyes characterised by the tetrazo component
    • C09B35/205Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of a diaryl- or triaryl- alkane or-alkene
    • C09B35/21Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of a diaryl- or triaryl- alkane or-alkene of diarylmethane or triarylmethane

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Luminescent Compositions (AREA)
  • Coloring (AREA)

Abstract

Disazodyes are made by combining the tetrazo compound of p-p1-diaminodiphenylmethane, p-p1-diaminotriphenylmethane, p-p1-diaminodiphenyldimethylmethane or their derivatives substituted in the aryl residues with two molecular proportions of combining components of which one at least is 2 : 8-dihydroxynaphthalene-6-sulphonic acid or a monoarylsulphonic acid ester of this acid. When the acid is used the dyestuff may further be esterified with an arylsulphochloride. In examples, (1) 4-41-diaminodiphenylmethane \sQ (in alkaline solution) 2 - 8 - dihydroxynaphthalene - 6 - sulphonic acid to give a dyestuff dyeing wool red shades; the dyestuff may further be esterified with p-toluenesulphochloride to give a dye which dyes wool yellowish-red shades; a similar product is obtained by using as a coupling component the monobenzenesulphonic acid ester of 2 : 8-dihydroxynaphthalene-6-sulphonic acid; (2) 4-41-diamino-3-31-dimethoxydiphenyldimethylmethane is tetrazotized and coupled in alkaline solution with one molecular proportion of 1-p-toluenesulphamino-8-hydroxynaphthalene-3-6-disulphonic acid and then with 2-8-dihydroxynaphthalene-6-sulphonic acid to give a bright claret red dyestuff; (3) 4-41-diaminodiphenylmethane \sQ 2,8-dihydroxynaphthalene-6-sulphonic acid to give a dyestuff dyeing wool red shades; the dyestuff may be further esterified to give a dyestuff of a brighter shade; (4) 4-41-diaminotriphenylmethane replaces the 4-41-diaminodiphenylmethane used in the previous example to give a red dyestuff which when esterified is brighter and yellower. Specifications 9642/89, [Class 2, Acids and salts, Organic &c.], 204,722 and 335,893, [both in Class 2 (iii), Dyes &c.], are referred to. Reference has been directed by the Comptroller to Specifications 206,831 and 244,782, [both in Class 2 (iii), Dyes &c.].
GB3534529A 1929-11-19 1929-11-19 The manufacture of acid disazodyestuffs Expired GB342807A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3534529A GB342807A (en) 1929-11-19 1929-11-19 The manufacture of acid disazodyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3534529A GB342807A (en) 1929-11-19 1929-11-19 The manufacture of acid disazodyestuffs

Publications (1)

Publication Number Publication Date
GB342807A true GB342807A (en) 1931-02-12

Family

ID=10376690

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3534529A Expired GB342807A (en) 1929-11-19 1929-11-19 The manufacture of acid disazodyestuffs

Country Status (1)

Country Link
GB (1) GB342807A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE745373C (en) * 1937-01-26 1944-03-21 Chem Ind Basel Process for the preparation of water-soluble acylaminoazo dyes
EP2163587A1 (en) * 2008-09-11 2010-03-17 Clariant International Ltd. Acid dyes

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE745373C (en) * 1937-01-26 1944-03-21 Chem Ind Basel Process for the preparation of water-soluble acylaminoazo dyes
EP2163587A1 (en) * 2008-09-11 2010-03-17 Clariant International Ltd. Acid dyes

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