GB457535A - Manufacture of 4-amino-6-methyl-3:4-dinitrodiphenylamine - Google Patents
Manufacture of 4-amino-6-methyl-3:4-dinitrodiphenylamineInfo
- Publication number
- GB457535A GB457535A GB16180/35A GB1618035A GB457535A GB 457535 A GB457535 A GB 457535A GB 16180/35 A GB16180/35 A GB 16180/35A GB 1618035 A GB1618035 A GB 1618035A GB 457535 A GB457535 A GB 457535A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dinitrodiphenylamine
- amino
- methyl
- manufacture
- sulphonic acid
- 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
4 - Amino - 6 - methyl - 3 : 4<1> - dinitrodiphenylamine is made by condensing 4-nitro-1-chlorobenzene-2-sulphonic acid with 1 : 4-diamino-3-nitro-6-methylbenzene and splitting off the sulphonic group from the 4-amino-6-methyl-3 : 4<1>-dinitrodiphenylamine - 2<1> - sulphonic acid thus obtained. It is an azo dye intermediate. In the example, the condensation is effected under pressure in presence of water and calcium carbonate and the sulphonic acid group is split off by heating with sulphuric acid. Specification 457,534 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE457534X | 1934-06-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB457535A true GB457535A (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 After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16178/35A Expired GB457534A (en) | 1934-06-02 | 1935-06-04 | Manufacture of 4-amino-3:4-dinitro-diphenylamine and of azo-dyestuffs therefrom |
Country Status (3)
Country | Link |
---|---|
FR (1) | FR790859A (en) |
GB (2) | GB457535A (en) |
NL (1) | NL40149C (en) |
Cited By (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
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3054792A (en) * | 1956-06-15 | 1962-09-18 | Ici Ltd | New triazino nitro dyestuffs |
Also Published As
Publication number | Publication date |
---|---|
GB457534A (en) | 1936-11-30 |
FR790859A (en) | 1935-11-28 |
NL40149C (en) |
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