GB629473A - Metallized azomethine dyes and nylon dyed therewith - Google Patents
Metallized azomethine dyes and nylon dyed therewithInfo
- Publication number
- GB629473A GB629473A GB34568/46A GB3456846A GB629473A GB 629473 A GB629473 A GB 629473A GB 34568/46 A GB34568/46 A GB 34568/46A GB 3456846 A GB3456846 A GB 3456846A GB 629473 A GB629473 A GB 629473A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- aminophenol
- nitro
- benzene
- hydroxy
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B55/00—Azomethine dyes
- C09B55/002—Monoazomethine dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Nylon is dyed using hot aqueous solutions of azomethine dyes containing cobalt in complex combination, which are free from sulphonic groups and have the formula <FORM:0629473/IV (c)/1> where R is a benzene radical having at least one nitro group, and R1 is a benzene or naphthalene radical which may be unsubstituted or may contain monovalent substituents such as nitro, halogen, amino, alkyl, alkoxy, hydroxy, or cyano. These dyestuffs are obtained by condensing an aromatic ortho-hydroxy amino compound of the benzene or naphthalene series with an ortho-hydroxy benzaldehyde substituted in the nucleus by one or more nitro groups, and heating the resulting azomethine dye, preferably after separation from the reaction mixture, with a solution of a salt of bivalent cobalt. Solvents for this reaction are water, alcohols, acetone, or esters. The cobalt compound may be added with the orthohydroxy-amino compound. Reactants specified are 2-aminophenol, 4-chloro-2-aminophenol, 2 - amino - 4.6 - dichlorophenol, 4 - or 5 - nitro-2 - aminophenol, 3 - amino - p - cresol, 4-aminoresorcin - 1 - methylether, 2 - aminoresorcinol, 6 - amino - 2 - cyanphenol, 2 - amino-1 - naphthol, and 2 - amino - 1.4 - dihydroxynaphthalene. The dyeing solutions may be acid or neutral and may contain surface-active agents and assistants such as ammonium chloride or sodium sulphate. In examples: 5-nitrosalicylaldehyde is reacted with (1) 2-aminophenol; (2) 4-chloro-2-aminophenol; (3) 4 - nitro - 2 - aminophenol; (4) 2 - amino-4.6 - dichlorophenol and the product is treated with ammonia and cobaltous chloride. Also, (5) 5-nitro-2-aminophenol is treated with cobaltous chloride in ethanol and then with 3-nitrosalicylaldehyde. An example of dyeing nylon with the product of (1) is given.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US629473XA | 1945-12-27 | 1945-12-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB629473A true GB629473A (en) | 1949-09-21 |
Family
ID=22045896
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB34568/46A Expired GB629473A (en) | 1945-12-27 | 1946-11-21 | Metallized azomethine dyes and nylon dyed therewith |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB629473A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2726920A (en) * | 1951-12-05 | 1955-12-13 | Basf Ag | Colored structures of polyamides and polyurethanes |
-
1946
- 1946-11-21 GB GB34568/46A patent/GB629473A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2726920A (en) * | 1951-12-05 | 1955-12-13 | Basf Ag | Colored structures of polyamides and polyurethanes |
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