GB439885A - Improvements in the manufacture and production of dyestuffs of the anthraquinone series - Google Patents
Improvements in the manufacture and production of dyestuffs of the anthraquinone seriesInfo
- Publication number
- GB439885A GB439885A GB1706034A GB1706034A GB439885A GB 439885 A GB439885 A GB 439885A GB 1706034 A GB1706034 A GB 1706034A GB 1706034 A GB1706034 A GB 1706034A GB 439885 A GB439885 A GB 439885A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alcohols
- condensed
- amino
- give
- blue
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Anthraquinone dyes are obtained by causing anthraquinones, negatively substituted, to react with aminophenylethyl alcohols, aminonaphthyl ethyl alcohols or their nuclear substitution products, or by causing aminoanthraquinones to react with halogen-substituted phenylethyl alcohols or naphthylethyl alcohols or their nuclear substitution products. The leuco anthraquinone compounds may be used. The products are suitable for dyeing cellulose esters and ethers. According to examples: (1) 1-chloranthraquinone is condensed with p-amino-phenylethylalcohol, and gives a rose-red dye for acetate-silk; 1 : 5-dichlor-, 1-amino-4-chlor-, 1 - amino - 4 - bromo - 2 - sulpho- and 1 : 4-diamino - 2 : 3 - dichloranthraquinones give in a similar manner bluish-red, blue-violet, and blue dyes, and leuco-quinizarin a blue green dye, respectively; (2) 1-aminoanthraquinone is condensed with p-chlorphenylethylalcohol to give a similar product to the first in example (1); (3) leucoquinizarin is condensed with 2 : 4-diaminophenylethyl alcohol e to give a green dye for acetate silk.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEI48449D DE609120C (en) | 1933-05-14 | 1933-05-14 | Process for the preparation of dyes of the anthraquinone series |
GB1706034A GB439885A (en) | 1934-06-08 | 1934-06-08 | Improvements in the manufacture and production of dyestuffs of the anthraquinone series |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1706034A GB439885A (en) | 1934-06-08 | 1934-06-08 | Improvements in the manufacture and production of dyestuffs of the anthraquinone series |
Publications (1)
Publication Number | Publication Date |
---|---|
GB439885A true GB439885A (en) | 1935-12-09 |
Family
ID=10088535
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1706034A Expired GB439885A (en) | 1933-05-14 | 1934-06-08 | Improvements in the manufacture and production of dyestuffs of the anthraquinone series |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB439885A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2641602A (en) * | 1950-11-29 | 1953-06-09 | Eastman Kodak Co | 1, 8-dihydroxy-5-nitro-4-hydroxyethylphenyl aminoanthraquinone compounds |
US3413257A (en) * | 1965-07-19 | 1968-11-26 | Ici Ltd | Coloration process |
-
1934
- 1934-06-08 GB GB1706034A patent/GB439885A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2641602A (en) * | 1950-11-29 | 1953-06-09 | Eastman Kodak Co | 1, 8-dihydroxy-5-nitro-4-hydroxyethylphenyl aminoanthraquinone compounds |
US3413257A (en) * | 1965-07-19 | 1968-11-26 | Ici Ltd | Coloration process |
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