GB457534A - Manufacture of 4-amino-3:4-dinitro-diphenylamine and of azo-dyestuffs therefrom - Google Patents
Manufacture of 4-amino-3:4-dinitro-diphenylamine and of azo-dyestuffs therefromInfo
- Publication number
- GB457534A GB457534A GB16178/35A GB1617835A GB457534A GB 457534 A GB457534 A GB 457534A GB 16178/35 A GB16178/35 A GB 16178/35A GB 1617835 A GB1617835 A GB 1617835A GB 457534 A GB457534 A GB 457534A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- dinitrodiphenylamine
- diazotized
- soaped
- rinsed
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/18—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides
- C09B29/20—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides of the naphthalene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Abstract
Azo dyes insoluble in water are made in substance, on the fibre or on a substratum by coupling diazotized 4 - amino - 3 : 4<1> - dinitrodiphenylamine with an arylide of 2 : 3-oxynaphthoic acid. Black-currant to black shades are obtained. They may be used for the production on the fibre of mixed shades with other dyes derived from 2 : 3-oxynaphthoic arylides, e.g. with those from diazotized 4-aminodiphenylamines. According to the examples: (1) cotton is impregnated with the a -naphthylamide by the usual process and developed with the diazo solution; (2) the material is prepared with the o-toluidide, printed with a paste containing the diazo compound, dried, treated with hot soda solution, rinsed and soaped; (3) crude, desized cotton piece goods are impregnated with the o-anisidide, passed through an acetic acid solution of the diazo compound, steamed, rinsed and soaped; (4) bleached cotton material is grounded with the o-anisidide, dried, passed through a solution containing diazotized 4-amino-4<1>-methoxydiphenylamine, diazotized 4 - amino - 3 : 4<1> - dinitrodiphenylamine and ammonium sulphate, steamed, rinsed and soaped; (5) the diazo compound is coupled in substance with the anilide. Other arylides are also specified. Specification 329,960, [Class 2 (iii)], is referred to. 4 - Amino - 3 : 4<1> - dinitrodiphenylamine is obtained by condensing 4-nitro-1-chlorobenzene-2-sulphonic acid with 1 : 4-diamino-3-nitrobenzene and splitting off the sulphonic group from the 4-amino-3 : 4<1>-dinitrodiphenylamine-2<1>-sulphonic acid thus obtained. According to the example, the condensation is effected under pressure in the presence of water and calcium carbonate and the sulphonic group is split off by heating with sulphuric acid. The Specification as open to inspection under Sect. 91 describes the preparation of 4-amino-6-methyl - 3 : 4<1> - dinitrodiphenylamine and mentions 6<1> - bromo - 2<1> : 3<1> - hydroxynaphthoyl - (1 - amino - 2 : 4 - dimethoxybenzene) and 6<1> - methoxy - 2<1> : 3<1> - hydroxynaphthoyl-(1-amino-2-methoxybenzene as coupling components. The use of the condensation product of oleyl alcohol and ethylene oxide in the printing paste of example 2 is also mentioned. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE457534X | 1934-06-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB457534A true GB457534A (en) | 1936-11-30 |
Family
ID=6539324
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16180/35A Expired GB457535A (en) | 1934-06-02 | 1935-06-04 | Manufacture of 4-amino-6-methyl-3:4-dinitrodiphenylamine |
GB16178/35A Expired GB457534A (en) | 1934-06-02 | 1935-06-04 | Manufacture of 4-amino-3:4-dinitro-diphenylamine and of azo-dyestuffs therefrom |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16180/35A Expired GB457535A (en) | 1934-06-02 | 1935-06-04 | Manufacture of 4-amino-6-methyl-3:4-dinitrodiphenylamine |
Country Status (3)
Country | Link |
---|---|
FR (1) | FR790859A (en) |
GB (2) | GB457535A (en) |
NL (1) | NL40149C (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3054792A (en) * | 1956-06-15 | 1962-09-18 | Ici Ltd | New triazino nitro dyestuffs |
-
0
- NL NL40149D patent/NL40149C/xx active
-
1935
- 1935-06-03 FR FR790859D patent/FR790859A/en not_active Expired
- 1935-06-04 GB GB16180/35A patent/GB457535A/en not_active Expired
- 1935-06-04 GB GB16178/35A patent/GB457534A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR790859A (en) | 1935-11-28 |
NL40149C (en) | |
GB457535A (en) | 1936-11-30 |
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