GB786928A - Improvements in or relating to 1,2 cobalt-complexes of monoazo-dyestuffs - Google Patents

Improvements in or relating to 1,2 cobalt-complexes of monoazo-dyestuffs

Info

Publication number
GB786928A
GB786928A GB35292/55A GB3529255A GB786928A GB 786928 A GB786928 A GB 786928A GB 35292/55 A GB35292/55 A GB 35292/55A GB 3529255 A GB3529255 A GB 3529255A GB 786928 A GB786928 A GB 786928A
Authority
GB
United Kingdom
Prior art keywords
hydroxy
methoxy
dyestuffs
methyl
propylamides
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
GB35292/55A
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.)
Sandoz AG
Original Assignee
Sandoz 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 Sandoz AG filed Critical Sandoz AG
Publication of GB786928A publication Critical patent/GB786928A/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
    • C09B45/20Monoazo compounds containing cobalt

Landscapes

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

Abstract

The invention comprises dyestuffs of formula <FORM:0786928/IV (b)/1> where v is H or Me, w is H, Cl, Me or NO2 and R is 31-methoxy- or 21-hydroxy-propyl, the NV group is in the 1 or 2 position of the naphthalene nucleus and o to the azo group, the SO2NHR group is in the 4, 5 or 6 position and A is A1, a compound of the same formula as A1, the residue of the dyestuff a 2-aminophenol-sulphonamide-\sY2 - (31 - chloro) - phenylnaphthylamine or the residue of a compound of formula <FORM:0786928/IV (b)/2> where X is OH or MeO, y is H, Me or CH3CONH, z is an alkyl group of up to 4 C atoms or the residue of an aliphatic, cycloaliphatic, araliphatic, aromatic or heterocyclic primary or secondary amine which may contain hydroxy, methoxy, ethoxy or methyl groups, R1 is an alkyl radicle of 6-18 C atoms and R2 is an alkyl or aryl radicle. They are made by treating appropriate dyestuffs or dyestuff mixtures with cobalt-yielding agents so that the final product contains approximately 2 mols. of dyestuff per atom of metal. Cobalting may be effected in conventional fashion, preferably with the use of cobaltous acetate, formate or sulphate in aqueous or organic media and especially in an aqueous caustic alkaline medium in the presence of compounds such as tartaric, citric or lactic acids. The dyestuffs dye wool, silk, leather and especially polyamide fibres from neutral to weakly acid baths in blue, green and olive shades. In examples illustrating the preparation of the dyestuffs and their use in dyeing processes the diazo components used are 4- and 5-nitro-, 4-chloro-, 5- and 6-nitro, 4-nitro-6-methyl-, 4,6-dinitro-2-aminophenols, 2-aminophenol-4- and -5-sulphonamides, -4-sulphonmethylamide, -(21-hydroxy, -methoxy and ethoxy) - ethylamides, -(21-hydroxy and 31-methoxy) - propylamides, - di - (21 - hydroxy-ethyl)amide, -cyclohexylamide, -benzylamide, -phenylamide, -(41-methyl)-phenylamide, -pyrrolidide and -morpholide, 2-aminophenol-6-methyl- and -acetylamino-4-sulphonamides, 2-amino - 1 - methoxybenzene - 4 - sulphonamide and 2 - amino - 1 - hydroxy - 4 - methyl - and -ethylsulphonylbenzenes, the coupling components being 2-naphthylamine-5 and 6-sulphon - (21 - hydroxy) - and - 6 - sulphon - (31-methoxy) - propylamides, 1 - naphthylamine-4- and -5-sulphon-(21-hydroxy and -methoxy)-propylamides and 2-methylaminophthalene-6-sulphon-(21-hydroxy and 31-methoxy)-propylamides, 2 - (31 - chloro) - phenylnaphthylamine, 1 - acetoacetylamino - 2 - ethylhexane, -octane, -hexane, -dodecane, -octadecane and -1,1-dimethyl -3,3 - dimethyl - butane and 1 - benzoylacetylaminooctane. Reference has been directed by the Comptroller to Specification 755,113.
GB35292/55A 1954-12-15 1955-12-08 Improvements in or relating to 1,2 cobalt-complexes of monoazo-dyestuffs Expired GB786928A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH786928X 1954-12-15

Publications (1)

Publication Number Publication Date
GB786928A true GB786928A (en) 1957-11-27

Family

ID=4536652

Family Applications (1)

Application Number Title Priority Date Filing Date
GB35292/55A Expired GB786928A (en) 1954-12-15 1955-12-08 Improvements in or relating to 1,2 cobalt-complexes of monoazo-dyestuffs

Country Status (1)

Country Link
GB (1) GB786928A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2631830A1 (en) * 1975-07-25 1977-02-10 Sandoz Ag ORGANIC COMPOUNDS

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2631830A1 (en) * 1975-07-25 1977-02-10 Sandoz Ag ORGANIC COMPOUNDS

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