GB652943A - Manufacture of xanthene dyestuffs - Google Patents
Manufacture of xanthene dyestuffsInfo
- Publication number
- GB652943A GB652943A GB1990848A GB1990848A GB652943A GB 652943 A GB652943 A GB 652943A GB 1990848 A GB1990848 A GB 1990848A GB 1990848 A GB1990848 A GB 1990848A GB 652943 A GB652943 A GB 652943A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxy
- fluoran
- followed
- manufacture
- mols
- 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
- C09B11/245—Phthaleins having both OH and amino substituent(s) on aryl ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Abstract
Dyes are made by sulphonating 3.6-di-(211.611-dimethyl - anilino) - 41 - hydroxy - 51 - carboxy - fluoran and/or the corresponding 51-hydroxy-41-carboxy fluoran. The products may be chromed. The starting material may be made by condensing one mol. 5-hydroxy-trimellitic acid with two mols. of (1) 3-hydroxy-21.61-dimethyldiphenylamine, (2) m - chlorphenol, followed by condensation with two mols. 2.6-dimethylaniline, or (3) resorcinol, followed by conversion of the fluorescein derivative so obtained to the 3.6-dichloro-fluoran, and condensation as under (2). An example is given of process (1), followed by sulphonation of the product. Specification 472,757 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1990848A GB652943A (en) | 1948-07-26 | 1948-07-26 | Manufacture of xanthene dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1990848A GB652943A (en) | 1948-07-26 | 1948-07-26 | Manufacture of xanthene dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB652943A true GB652943A (en) | 1951-05-02 |
Family
ID=10137139
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1990848A Expired GB652943A (en) | 1948-07-26 | 1948-07-26 | Manufacture of xanthene dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB652943A (en) |
-
1948
- 1948-07-26 GB GB1990848A patent/GB652943A/en not_active Expired
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