GB312330A - - Google Patents
Info
- Publication number
- GB312330A GB312330A GB16093/29A GB1609329A GB312330A GB 312330 A GB312330 A GB 312330A GB 16093/29 A GB16093/29 A GB 16093/29A GB 1609329 A GB1609329 A GB 1609329A GB 312330 A GB312330 A GB 312330A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- acids
- monoazo
- dyes
- dyestuff
- 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
- C09B43/00—Preparation of azo dyes from other azo compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
312,330. Geigy Akt.-Ges., J. R. May 24, 1928, [Convention date]. Monoazo dyes; phthalein dyes. - Monoazo phthalein dyes are obtained bv condensing arylazoresorcinols with N-alkylated or N-arylated aminooxybenzoylbenzoic acids or aminooxybenzoylpropionic acids in equimolecular proportions. The products are mordant dyestuffs, those obtained from diazotized o-oxyamines yielding mainly blue to greenish-blue dyeings when aftertreated on the fibre with metal salts; the presence of additiona.l mordant-dyeing groups, such as carboxyl or o-oxycarboxyl groups in the arylazoresorcinol results in dyeings which are red to brown-red on after-chroming. The following examples are specified. (1) A mixture of the monoazo dyestuff 6-methyl-2-aminophenol-4-sulphonic acid # resorcinol with dimethylaminooxybenzoylbenzoic acid is heated with concentra,ted sulphuric acid for 20 hrs. at 70‹ C., and the dyestuff is precipitated by pouring into water; it dyes wool from an acid bath a reddishblue which is rendered a fast blue by aftertreatment; a similar product is obtained when 4-chloro-2-aminophenol-6-sulphonic acid is used as first component. (2) A mixture of the monoazo dyestuff 1:2: 4-aminonaphtholsulphonic acid # resorcinol and diethylaminooxybenzoylbenzoic acid is heated with concentrated sulphuric acid for 4-5 hrs. at 70‹ C., and the product is separated as in (1); it dyes wool from an acid bath a pure greenish-blue which is rendered duller but faster by after-chroming or after-coppering; the corresponding dyestuff obtained when nitro -1:2:4- aminonaphtholsulphonic acid is used as first component yields green dyeings when after-chromed on wool. (3) A mixture of the monoazo dyestuff anthranilic acid # resorcinol and dimethylaminooxy. benzoylbenzoic acid is heated with concentrated sulphuric acid for 24 hrs. at 70‹ C., and the product is separated as in (1); it yields brownred dyeings when after-chromed on wool. The use as first components of aniline and its sulphonic acids, e.g. sulphanilic acid, chloranilinesulphonic acid, naphthylamines or their sulphonic acids, e.g. 1 :5- or 2 : 6-naphthylaminesulphonic acids gives rise to brown to red dyestuffs, valuable mainly as intermediates. Specifications 12181/97 and 10523/11 are referred to. The Specification as open to inspection under Sect. 91 (3) (a) comprises also the use of derivatives of resorcinol as coupling components. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE312330T | 1928-05-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB312330A true GB312330A (en) | 1930-08-07 |
Family
ID=31894625
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16093/29A Expired GB312330A (en) | 1928-05-24 | 1929-05-24 |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB312330A (en) |
-
1929
- 1929-05-24 GB GB16093/29A patent/GB312330A/en not_active Expired
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