GB251644A - Improved manufacture of acid dyestuffs of the rhodamine series - Google Patents
Improved manufacture of acid dyestuffs of the rhodamine seriesInfo
- Publication number
- GB251644A GB251644A GB11311/26A GB1131126A GB251644A GB 251644 A GB251644 A GB 251644A GB 11311/26 A GB11311/26 A GB 11311/26A GB 1131126 A GB1131126 A GB 1131126A GB 251644 A GB251644 A GB 251644A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dyes
- dyestuff
- phthalic anhydride
- sulphonation
- rhodamine
- 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
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
- C09B11/10—Amino derivatives of triarylmethanes
- C09B11/24—Phthaleins containing amino groups ; Phthalanes; Fluoranes; Phthalides; Rhodamine dyes; Phthaleins having heterocyclic aryl rings; Lactone or lactame forms of triarylmethane dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
Abstract
251,644. Soc. Anon. Durand et Huguenin. May 4, 1925, [Convention date]. Phthalein dyes.-Acid dyes of the rhodamine series are obtained by condensing an aryl-maminophenol with phthalic anhydride, or a substitution product thereof, in presence of a sulphonating agent, whereby the formation and sulphonation of the dyestuff takes place in one operation. In examples (1) o-tolyl-m-aminophenol. phthalic anhydride and sulphuric acid mono-hydrate are melted together and maintained at a temperature of 140-170‹ C. until the mass solidifies, when the dyestuff is dissolved in dilute alkali and isolated by salting out or evaporation; it dyes wool in clear bluish-red tints, which are redder than those yielded by the dyestuff obtained by a subsequent sulphonation of the corresponding rhodamine, and (2) xylidylm-aminophenol (from 1 : 3-dimethyl-2-aminobenzene and resorcinol) and phthalic anhydride are melted together, sulphuric acid monohydrate is added gradually to the molten mass, which is then kept at 170‹ C. until it solidifies; the product, isolated in the same manner as in example (1), dyes wool clear red tints, which are more yellowish than those obtained with the body made by subsequent sulphonation. Substituted phthalic anhydrides, such as dichlor- or tetrachlor-phthalic anhydrides, may be used.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE251644X | 1925-05-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB251644A true GB251644A (en) | 1927-07-29 |
Family
ID=5943951
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB11311/26A Expired GB251644A (en) | 1925-05-04 | 1926-04-29 | Improved manufacture of acid dyestuffs of the rhodamine series |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB251644A (en) |
-
1926
- 1926-04-29 GB GB11311/26A patent/GB251644A/en not_active Expired
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