GB1358488A - Oxazine dyestuffs - Google Patents
Oxazine dyestuffsInfo
- Publication number
- GB1358488A GB1358488A GB2159372A GB2159372A GB1358488A GB 1358488 A GB1358488 A GB 1358488A GB 2159372 A GB2159372 A GB 2159372A GB 2159372 A GB2159372 A GB 2159372A GB 1358488 A GB1358488 A GB 1358488A
- Authority
- GB
- United Kingdom
- Prior art keywords
- nitroso compound
- optionally
- alkyl
- oxazine
- aminophenol
- 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
- C09B19/00—Oxazine dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Coloring (AREA)
Abstract
1358488 Preparing oxazine dyes IMPERIAL CHEMICAL INDUSTRIES Ltd 20 Nov 1972 [9 May 1972] 21593/72 Heading C4P Oxazine dyestuffs of the general formula wherein R, R<SP>1</SP> and R<SP>2</SP> are optionally substituted alkyl, aralkyl or aryl groups or R and R<SP>1</SP> together with the nitrogen atom and optionally other hetero atoms may form a heterocyclic ring, R<SP>3</SP> is H, alkyl or aralkyl or R<SP>2</SP> and R<SP>3</SP> together with the nitrogen atom and optionally other hetero atoms may form a heterocyclic ring, rings X and Y may be further substituted by alkyl groups and 2<SP>(-)</SP> is an anion are prepared by nitrosating an amine of the general formula in an aqueous acidic medium and without isolation of the nitroso compound formed the aqueous suspension of the nitroso compound is reacted with a m-aminophenol of the formula at a pH of 1À0 to 4À5, and preferably at 65-100‹ C. using 1À3 to 1-6 moles of nitroso compound per mole of m-aminophenol. The dyes give greenblue shades on polymers and copolymers of acrylonitrile and dicyanoethylene.
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2159372A GB1358488A (en) | 1972-05-09 | 1972-05-09 | Oxazine dyestuffs |
DE19722259341 DE2259341A1 (en) | 1972-05-09 | 1972-12-04 | PROCESS FOR THE PREPARATION OF OXAZINE DYES |
JP12195472A JPS4923226A (en) | 1972-05-09 | 1972-12-05 | |
IT3261772A IT971650B (en) | 1972-05-09 | 1972-12-06 | OXZIN DYES |
NL7216600A NL7216600A (en) | 1972-05-09 | 1972-12-07 | |
FR7243873A FR2183653B3 (en) | 1972-05-09 | 1972-12-08 | |
ES409606A ES409606A1 (en) | 1972-05-09 | 1972-12-14 | Oxazine dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2159372A GB1358488A (en) | 1972-05-09 | 1972-05-09 | Oxazine dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1358488A true GB1358488A (en) | 1974-07-03 |
Family
ID=10165533
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2159372A Expired GB1358488A (en) | 1972-05-09 | 1972-05-09 | Oxazine dyestuffs |
Country Status (7)
Country | Link |
---|---|
JP (1) | JPS4923226A (en) |
DE (1) | DE2259341A1 (en) |
ES (1) | ES409606A1 (en) |
FR (1) | FR2183653B3 (en) |
GB (1) | GB1358488A (en) |
IT (1) | IT971650B (en) |
NL (1) | NL7216600A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5917035A (en) * | 1992-12-15 | 1999-06-29 | Ciba Specialty Chemicals Corporation | Oxazine dyes, their preparation and the use thereof |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH593321A5 (en) * | 1974-04-29 | 1977-11-30 | Ciba Geigy Ag | |
JPS52138774U (en) * | 1976-04-15 | 1977-10-21 |
-
1972
- 1972-05-09 GB GB2159372A patent/GB1358488A/en not_active Expired
- 1972-12-04 DE DE19722259341 patent/DE2259341A1/en active Pending
- 1972-12-05 JP JP12195472A patent/JPS4923226A/ja active Pending
- 1972-12-06 IT IT3261772A patent/IT971650B/en active
- 1972-12-07 NL NL7216600A patent/NL7216600A/xx unknown
- 1972-12-08 FR FR7243873A patent/FR2183653B3/fr not_active Expired
- 1972-12-14 ES ES409606A patent/ES409606A1/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5917035A (en) * | 1992-12-15 | 1999-06-29 | Ciba Specialty Chemicals Corporation | Oxazine dyes, their preparation and the use thereof |
Also Published As
Publication number | Publication date |
---|---|
IT971650B (en) | 1974-05-10 |
JPS4923226A (en) | 1974-03-01 |
FR2183653A1 (en) | 1973-12-21 |
ES409606A1 (en) | 1975-12-16 |
NL7216600A (en) | 1973-11-13 |
FR2183653B3 (en) | 1976-01-09 |
DE2259341A1 (en) | 1973-11-29 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |