GB315400A - Manufacture of new dyestuffs - Google Patents
Manufacture of new dyestuffsInfo
- Publication number
- GB315400A GB315400A GB19133/29A GB1913329A GB315400A GB 315400 A GB315400 A GB 315400A GB 19133/29 A GB19133/29 A GB 19133/29A GB 1913329 A GB1913329 A GB 1913329A GB 315400 A GB315400 A GB 315400A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- aminophenol
- dyestuff
- dyestuffs
- oxidized
- 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/48—Preparation from other complex metal compounds of azo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Abstract
315,400. Soc. of Chemical Industry in Basle. July 13. 1928, [Convention date]. Azo dyes are made (1) by treating with an oxidizing agent metal compounds of the dyestuffs o-oxy- or o-carboxyamine # J-acid, 2:8:6-acid or 1-sulpho J acid or o-oxy or o-carboxypolyazo dyestuffs containing these end components, or (2) by treating the above metal-free dyestuffs first with an oxidizing agent and then with compounds yielding metal. They dye cotton, wool and viscose silk generally in grey tints. In examples, (1) the dyestuff 4-chloro-2-aminophenol-6-sulphonic acid # J acid is treated with ammoniacal copper oxide and the product dried with free access of air; glycerine or an oxygen carrier may be added; (2) an ammoniacal solution of the copper compound of the dyestuff in (1) is oxidized by air in the presence or absence of an oxygen carrier, e.g. a copper or vanadium salt; (U) a caustic soda solution of the same copper compound is oxidized with potassium ferricyanide, an alkali perborate or persulphate, or lead peroxide; (4) an alkaline solution of the chromium compound of the dyestuff from nitrated 1-diazo-2-naphthol-4-sulphonic acid and J acid is oxidized with potassium hypochlorite; (5) the zinc compound of the dyestuff in 1 is oxidized with alkali hypochlorite; (6) the copper compound of the dyestuff 2-aminophenol-4: 6-disulphonic acid # J acid is oxidized in acetic acid with potassium bichromate; (7) a current of air is passed through a boiling ammoniacal solution of the copper compound obtained as in example 1; the oxidation may be effected under pressure above 100‹ C.; (8) the product obtained by oxidizing the dyestuff 4-nitro-2-aminophenol-6- sulphonic acid # J acid with alkali hypochlorite is converted into the copper compound. A table is given showing the shades produced from metalliferous dyestuffs using the following additional diazo components before and after oxidation with hypochlorite : 6-carboxy-4-sulpho-2- aminophenol, 4- and 5-nitro-2-aminophenol, 2- diazo-1-naphthol-4: 8-disulphonic acid, anthranilic acid, o-aminophenol-4-sulphonic acid, and the aminoazo product 4-chlor-2-aminophenol-6-sulphonic acid # (alkaline) J acid. Specification 296,680 is referred to. 6-Carboxy-4-sulpho-2-amino-1-phenol is made by sulphonating salicylic acid, nitrating and reducing. The Specification as open to inspection under Sect. 91 (3) (a) comprises also azo dyestuffs obtained (1) by treating metal compounds of azo dyestuffs in general with oxidizing agents and (2) by treating any suitable azo dyestuff first with an oxidizing agent and then with a metal compound. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH315400X | 1928-07-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB315400A true GB315400A (en) | 1930-10-21 |
Family
ID=4495981
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB19133/29A Expired GB315400A (en) | 1928-07-13 | 1929-06-21 | Manufacture of new dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB315400A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4988805A (en) * | 1987-07-29 | 1991-01-29 | Bayer Aktiengesellschaft | Naphtholazophenylazoaminonaphthol compounds and copper complexes thereof |
-
1929
- 1929-06-21 GB GB19133/29A patent/GB315400A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4988805A (en) * | 1987-07-29 | 1991-01-29 | Bayer Aktiengesellschaft | Naphtholazophenylazoaminonaphthol compounds and copper complexes thereof |
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