GB287995A - Improvements in the manufacture of triarylmethane dyes - Google Patents
Improvements in the manufacture of triarylmethane dyesInfo
- Publication number
- GB287995A GB287995A GB334027A GB334027A GB287995A GB 287995 A GB287995 A GB 287995A GB 334027 A GB334027 A GB 334027A GB 334027 A GB334027 A GB 334027A GB 287995 A GB287995 A GB 287995A
- Authority
- GB
- United Kingdom
- Prior art keywords
- naphthalenedisulphonate
- acid
- manufacture
- hydrol
- oxidized
- 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
- C09B11/12—Amino derivatives of triarylmethanes without any OH group bound to an aryl nucleus
- C09B11/16—Preparation from diarylketones or diarylcarbinols, e.g. benzhydrol
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Detergent Compositions (AREA)
Abstract
287,995. British Dyestuffs Corporation, Ltd., and Simmons, T. A. Feb. 5, 1927. Triarylmethane dyes.-In the manufacture of Lissamine green V (Colour Index No. 735) from 4 : 4<1>-tetraethyldiaminobenzhydrol and 2: 7- naphthalenedisulphonic acid, the hydrol is isolated in the form of its, 2 : 7-naphthalenedisulphonate. In an example, 4 : 4-tetraethyldiaminodiphenylmethane is oxidized with lead peroxide in order to form the hydrol. After removing the lead from solution, the 2 : 7-naphthalenedisulphonate is precipitated by adding sodium 2: 7-naphthalenedisulphonate and acidifying with sulphuric acid. To prepare the dyestuff, the naphthalenedisulphonate is washed and dissolved in sulpburic acid. The leuco dyestuff obtained by heating and pouring into water is then oxidized with lead peroxide in the usual manner. In preparing the 2 : 7-naphthalenedisulphonate anv soluble salt of 2: 7-naphthalenedisulphonic acid may be used.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB334027A GB287995A (en) | 1927-02-05 | 1927-02-05 | Improvements in the manufacture of triarylmethane dyes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB334027A GB287995A (en) | 1927-02-05 | 1927-02-05 | Improvements in the manufacture of triarylmethane dyes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB287995A true GB287995A (en) | 1928-04-05 |
Family
ID=9756463
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB334027A Expired GB287995A (en) | 1927-02-05 | 1927-02-05 | Improvements in the manufacture of triarylmethane dyes |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB287995A (en) |
-
1927
- 1927-02-05 GB GB334027A patent/GB287995A/en not_active Expired
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