GB254708A - Manufacture of new azo-dyestuffs and chromium derivatives thereof - Google Patents

Manufacture of new azo-dyestuffs and chromium derivatives thereof

Info

Publication number
GB254708A
GB254708A GB16012/26A GB1601226A GB254708A GB 254708 A GB254708 A GB 254708A GB 16012/26 A GB16012/26 A GB 16012/26A GB 1601226 A GB1601226 A GB 1601226A GB 254708 A GB254708 A GB 254708A
Authority
GB
United Kingdom
Prior art keywords
sulphamide
pyrazolone
aminophenol
phenyl
chromium
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
GB16012/26A
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 Schweiz AG
Original Assignee
Gesellschaft fuer Chemische Industrie in Basel CIBA
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 Gesellschaft fuer Chemische Industrie in Basel CIBA filed Critical Gesellschaft fuer Chemische Industrie in Basel CIBA
Publication of GB254708A publication Critical patent/GB254708A/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
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/34Monoazo dyes prepared by diazotising and coupling from other coupling components
    • C09B29/36Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
    • C09B29/3604Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
    • C09B29/3647Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms
    • C09B29/3652Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms containing a 1,2-diazoles or hydrogenated 1,2-diazoles
    • C09B29/366Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms containing a 1,2-diazoles or hydrogenated 1,2-diazoles containing hydroxy-1,2-diazoles, e.g. pyrazolone

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

254,708. Soc. of Chemical Industry in Basle. July 3, 1925, [Convention date]. Monoazo dyes and chromium compounds thereof.-Monoazo dyes are obtained by coupling an unsulphonated o-oxydiazo compound with an unsulphonated 1-aryl-5-pyrazolene, at least one of the components containing a sulphamido group. The products may be converted into chromium compounds by treating with agents which yield chromium; these dya wool, particularly loose wool or cardings, very equal orange tints fast to fulling and light. In examples 6-nitro-2-aminophenol-4-sulphamide (obtained by nitrating 2- aminophenol-4-sulphamide) is diazotized and coupled with 1-phenyl-3-methyl-5-pyrazolone and 2-aminophenol-4-sulphamide is diazotized and coupled with 1- (3<1>-sulphamido) -phenyl-3- methyl-5-pyrazolone; the dyestuffs from 4-nitro-2- aminophenol and 1-(3<1>-sulphamido)-phenyl-3- methyl- (or carboxyl) -5-pyrazolone are also referred to. In further examples, the dyestuff from 2-amirophenol-4-sulphamide and 1- (3<1>-sulphamido) -phenyl-3-methyl-5-pyrazolone is treated with chromium formate or sodium chromate, the dyestuff from 6-nitro-2-aminophenol-4-sulphamide and 1-phenyl-3-methyl-5-pyrazolone is treated with chromium acetate, and the dyestuff from 2-aminophenol-4-sulphamide and 1- (3<1>- sulphamido) - phenyl-5-pyrazolone-3-carboxylic acid is treated with a paste containing hydrated chromium oxide, caustic potash and glycerine, to yield the corresponding chromium compounds. Specifications 126,460 and 210,699 are referred to.
GB16012/26A 1925-07-03 1926-06-25 Manufacture of new azo-dyestuffs and chromium derivatives thereof Expired GB254708A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH254708X 1925-07-03

Publications (1)

Publication Number Publication Date
GB254708A true GB254708A (en) 1927-06-09

Family

ID=4470705

Family Applications (1)

Application Number Title Priority Date Filing Date
GB16012/26A Expired GB254708A (en) 1925-07-03 1926-06-25 Manufacture of new azo-dyestuffs and chromium derivatives thereof

Country Status (1)

Country Link
GB (1) GB254708A (en)

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