GB421610A - Manufacture of azo-dyestuffs insoluble in water - Google Patents

Manufacture of azo-dyestuffs insoluble in water

Info

Publication number
GB421610A
GB421610A GB18193/33A GB1819333A GB421610A GB 421610 A GB421610 A GB 421610A GB 18193/33 A GB18193/33 A GB 18193/33A GB 1819333 A GB1819333 A GB 1819333A GB 421610 A GB421610 A GB 421610A
Authority
GB
United Kingdom
Prior art keywords
amino
benzene
hydroxy
chlorobenzene
diazotized
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
GB18193/33A
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 GB421610A publication Critical patent/GB421610A/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
    • C09B29/24Monoazo dyes prepared by diazotising and coupling from coupling components containing both hydroxyl and amino directing groups
    • C09B29/28Amino naphthols
    • 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
    • C09B35/08Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl

Landscapes

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

Abstract

Azo dyes; lakes; azo dyes, forming upon the material; printing.--Azo dyestuffs, insoluble in water, are manufactured by coupling, in substance, on the fibre or on substrata, a diazo-, tetrazo- or diazo - azo - compound with a 1-hydroxy-3 : 5-diarylaminobenzene (obtainable by condensing phloroglucinol with the appropriate aminoaryl compound), only such components being used as do not contain any group lending solubility. In examples: (1) cotton yarn is impregnated with a solution of 1-hydroxy-3 : 5-diphenylaminobenzene or the corresponding di-(4<1>-methylphenylamino)- or di - (2<1> - 4<1> - dimethylphenylamino) - compounds, and developed with diazotized 1-amino-2 : 5-dichlorobenzene, yielding yellow-brown dyeings; (2) an orange-brown dyeing is similarly obtained from 1 - hydroxy - 3 : 5 - di - (4<1> - methoxyphenylamino) - benzene and diazotized 1 - amino - 2 - (4<1> - chlorophenoxy) - 5 - chlorobenzene; the same coupling component yields a deep reddish-brown dyeing with tetrazotized 4 : 4<1>-diamino-3 : 3<1>-dichlorodiphenyl and a brownish garnet with diazotized 4 - amino - 3 : 2<1> - dimethylazo-benzene. The Specification as open to inspection under Sect. 91 comprises also the following subject-matter: (a) the first dyestuff of (2) above may be prepared by the nitrosamine printing process, by printing with a mixture prepared from an alkali salt of the nitrosamine of 1-amino-2-(4<1>-chlorophenoxy)-5-chlorobenzene and an alkali salt of 1-hydroxy-3 : 5-di-(4<1>-methoxyphenylamino)-benzene; (b) wool is grounded with a caustic soda solution of 1-hydroxy-3 : 5-di-(4<1>-chlorophenylamino)-benzene and developed with diazotized 1-amino-2-phenoxy-5-chlorobenzene, yielding a yellow-brown dyeing; (c) in an additional example the dyestuff 1-amino-2-chloro - 4 - nitrobenzene --> 1 - hydroxy - 3 : 5-di-(4<1>-methylphenylamino)-benzene is prepared in substance, and yields a brown lake when mixed with substrata; (d) a table gives the shades obtained from additional dyestuffs, the following additional components being specified: diazo-components: 1-amino-3-chlorobenzene, 1-amino-2-methoxy-4-nitrobenzene, 1-amino-2-methoxy-5-(diethylaminosulphonyl)-benzene, 1-amino-2-methoxy-5-chlorobenzene, 4-amino-4<1>-methoxydiphenylamine, 1-amino-2 : 4 : 5-trichlorobenzene, 1-aminoanthraquinone, 2-amino - 1 : 6 - dibromonaphthalene, 1 - amino - 2 - (2<1> : 5<1> - dichlorophenoxy) - 5 - chlorobenzene, 1 - amino - 2 - chloro - 5 - trifluoromethylbenzene, 1-amino-4-benzoylamino-2 : 5-diethoxybenzene, 1-amino-3-benzoylbenzene, 1-amino-2-methyl-5 - (carbonyl - [1<1> - amino - 2<1> : 5<1> - dimethoxy - benzene])-benzene, 3-aminocarbazole, 4 : 4<1>-diamino-3 : 3<1>-dimethoxydiphenyl, 1-amino-4-benzoylamino-2 : 5-dichlorobenzene, 1-amino-3 - methyl - 2 : 4 - dichlorobenzene, 1 - amino - 2 - phenylsulphonylbenzene; coupling components: 1 - hydroxy - 3 : 5 - di - (4<1>-ethoxyphenylamino) - benzene, 1-hydroxy-3 : 5-di-(4<1>-phenoxyphenylamino) - benzene, 1 - hydroxy - 3 : 5 - di - (3<1> - 4<1> dichlorophenylamino) - benzene, 1 - hydroxy - 3 : 5 - di - (3<1> - methylphenylamino) - benzene, 1-hydroxy-3 : 5-di-(2<1>-methyl-4<1>-chlorophenylamino) - benzene, 1 - hydroxy - 3 : 5 - di - (2<1> - methoxy - 4<1> - chlorophenylamino) - benzene, 1 - hydroxy - 3 : 5 - di - (4<1> - acetylaminophenylamino) - benzene, 1 - hydroxy - 3 : 5 - di - (naphthyl - 2<1> - amino) - benzene, 1 - hydroxy - 3 : 5 - di - (quinolyl - 6<1> - amino) - benzene, 1 - hydroxy - 3 : 5-di-(4<1>-chloro-3<1>-nitrophenylamino)-benzene, 1 - hydroxy - 3 : 5 - di - (4<1> - [4<11> - methoxyphenylamino] - phenylamino) - benzene, 1 - hydroxy - 3 : 5 - di - (3<1> - methoxynaphthyl - 2<1>-amino)-benzene. This subject-matter does not appear in the Specification as accepted.
GB18193/33A 1932-06-25 1933-06-26 Manufacture of azo-dyestuffs insoluble in water Expired GB421610A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE421610X 1932-06-25

Publications (1)

Publication Number Publication Date
GB421610A true GB421610A (en) 1934-12-27

Family

ID=6458971

Family Applications (1)

Application Number Title Priority Date Filing Date
GB18193/33A Expired GB421610A (en) 1932-06-25 1933-06-26 Manufacture of azo-dyestuffs insoluble in water

Country Status (1)

Country Link
GB (1) GB421610A (en)

Similar Documents

Publication Publication Date Title
GB457763A (en) Improvements relating to the production of insoluble azo dyestuffs on textile fibres
GB421610A (en) Manufacture of azo-dyestuffs insoluble in water
US2144578A (en) Process for producing fast dyeings on the fiber
US2155685A (en) Azo dyes
GB536159A (en) Manufacture of brown polyazo dyestuffs, especially suitable for dyeing leather
GB457534A (en) Manufacture of 4-amino-3:4-dinitro-diphenylamine and of azo-dyestuffs therefrom
US2243014A (en) Manufacture of disazo dyestuffs
GB424262A (en) Manufacture of azo-dyestuffs suitable for dyeing leather
GB441178A (en) Manufacture of azo-dyestuffs
GB481747A (en) Manufacture of azo-dyestuffs insoluble in water
GB216527A (en) Manufacture of azo-dyestuffs
GB193834A (en) Manufacture of azo-dyestuffs
GB426564A (en) Process for the manufacture of water-insoluble azodyestuffs
GB299791A (en) Manufacture of azo-dyestuffs
GB437675A (en) Manufacture of arylides from 4-hydroxydiphenyl-3-carboxylic acid and of azo-dyestuffs therefrom
GB423736A (en) Manufacture of azo-dyestuffs insoluble in water
GB245790A (en) Process of dyeing cellulose esters and ethers
GB587348A (en) Manufacture of disazo-dyestuffs
GB248766A (en) Manufacture of azo-dyestuffs
GB421611A (en) Manufacture of 4:8-dihydroxy-1:2:5:6-dibenzophenazines and azo-dyestuffs therefrom
GB311400A (en) Manufacture of azo-dyestuffs, dyeing black tints
GB379555A (en) Manufacture of azo-dyestuffs on the fibre
GB400920A (en) Improvements in the manufacture and production of water-soluble azo dystuffs
GB488595A (en) Improvements in azo-dyestuffs
GB303424A (en) Improvements in the manufacture and production of a black trisazo dyestuff