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GB849705A - 1,2-chromium-containing benzene-monoazo-pyrazolene dyestuff complexes - Google Patents

1,2-chromium-containing benzene-monoazo-pyrazolene dyestuff complexes

Info

Publication number
GB849705A
GB849705A GB24450/58A GB2445058A GB849705A GB 849705 A GB849705 A GB 849705A GB 24450/58 A GB24450/58 A GB 24450/58A GB 2445058 A GB2445058 A GB 2445058A GB 849705 A GB849705 A GB 849705A
Authority
GB
United Kingdom
Prior art keywords
alkyl
dyes
halo
nitro
complexes
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
GB24450/58A
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.)
Bayer AG
Original Assignee
Bayer 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 Bayer AG filed Critical Bayer AG
Publication of GB849705A publication Critical patent/GB849705A/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
    • C09B45/00Complex metal compounds of azo dyes
    • C09B45/02Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
    • C09B45/14Monoazo compounds
    • C09B45/16Monoazo compounds containing chromium

Landscapes

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

Abstract

The invention comprises 1, 2 chromium complexes of dyes of formula: <FORM:0849705/IV (c)/1> where R is the residue of 4-nitro- or a 4- halo-or -alkyl-, 6-nitro -4- alkyl- or -halo -4, 6-dihalo-, 6-alkyl- or -halo-4-nitro-2-aminophenol or an O-alkyl ether or ester thereof, R1 is a sulphonamide group which may be alkyl substituted and Z is a substituent other than SO3H or COOH. The complexes are formed in substance, or on the fibre, by conventional processes from the metalfree dyes which are themselves prepared by usual methods. Alkyl and halogen groups are indicated for Z, specified pyrazolones from which the dyes are derived including 1-(21-methyl -61-chloro -41- sulphamido and -methylsulphamido)-and -(21, 61-dimethyl -31- and 41-sulphamido)-phenyl -3- methyl -5- pyrazolones. Wool and similar materials such as silk, leather, polyamides and polyurethanes, preferably dyed from neutral to organic acid baths, are dyed in bluish red shades. Examples are provided of the preparation of the dyes and their use in dyeing processes. Specification 740,589 and 758,016 are referred to.
GB24450/58A 1957-08-07 1958-07-29 1,2-chromium-containing benzene-monoazo-pyrazolene dyestuff complexes Expired GB849705A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE849705X 1957-08-07

Publications (1)

Publication Number Publication Date
GB849705A true GB849705A (en) 1960-09-28

Family

ID=6775924

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24450/58A Expired GB849705A (en) 1957-08-07 1958-07-29 1,2-chromium-containing benzene-monoazo-pyrazolene dyestuff complexes

Country Status (1)

Country Link
GB (1) GB849705A (en)

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