GB443841A - Process for the manufacture of azodyestuffs - Google Patents
Process for the manufacture of azodyestuffsInfo
- Publication number
- GB443841A GB443841A GB2569234A GB2569234A GB443841A GB 443841 A GB443841 A GB 443841A GB 2569234 A GB2569234 A GB 2569234A GB 2569234 A GB2569234 A GB 2569234A GB 443841 A GB443841 A GB 443841A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- amino
- acetyl
- sulphonic acid
- cotton
- 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/02—Disazo dyes
- C09B31/08—Disazo dyes from a coupling component "C" containing directive hydroxyl and amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Paper (AREA)
Abstract
Secondary disazo dyes are made by coupling diazotized monoamines of the diphenyl series with 1-amino-2-naphtholalkyl ethers, again diazotizing and coupling with non-diazotizable 1-acylamino-8-naphtholsulphonic acids. They dye cotton in clear green to bluish greenshades and some are suitable for dyeing viscose, leather, paper and jute. In examples the following dyes are described: (1) 4-amino-diphenyl - 3 - sulphonic acid --> 1 - amino - 2 - ethoxy or methoxynaphthalene-6-sulpho acid --> N-benzoyl-H acid (green on viscose and cotton); (2) 2-aminodiphenyl-5-sulphonic acid --> 1-amino-2-ethoxynaphthalene-6-sulphonic acid --> N-acetyl-H acid (bluish-green on cotton). Other components specified are 1-acetylamino-8-naphthol- 6-sulphonic acid, N-benzoyl- or acetyl-K acid, 1-acetyl-, propionyl-, chloracetyl - or benzoylamino - 8 - naphthol - 4 - sulpho- or 2 : 4-disulpho acids. Unsulphonated 1 - amino - 2 - naphtholalkyl ethers may also be used as middle components.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2569234A GB443841A (en) | 1934-09-06 | 1934-09-06 | Process for the manufacture of azodyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2569234A GB443841A (en) | 1934-09-06 | 1934-09-06 | Process for the manufacture of azodyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB443841A true GB443841A (en) | 1936-03-06 |
Family
ID=10231741
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2569234A Expired GB443841A (en) | 1934-09-06 | 1934-09-06 | Process for the manufacture of azodyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB443841A (en) |
-
1934
- 1934-09-06 GB GB2569234A patent/GB443841A/en not_active Expired
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