GB1020304A - Phthalocyanine dyestuffs - Google Patents
Phthalocyanine dyestuffsInfo
- Publication number
- GB1020304A GB1020304A GB1447564A GB1447564A GB1020304A GB 1020304 A GB1020304 A GB 1020304A GB 1447564 A GB1447564 A GB 1447564A GB 1447564 A GB1447564 A GB 1447564A GB 1020304 A GB1020304 A GB 1020304A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- radical
- dyes
- phthalocyanine
- quinoxaline
- 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
- C09B62/36—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to some other heterocyclic ring
- C09B62/42—Porphines; Azaporphines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
The invention comprises phthalocyanine dyes which, in the free acid state, have the formula <FORM:1020304/C4-C5/1> where Ap is a metal phthalocyanine dyestuff radical, R is a carbocyclic aromatic radical, X and Y are each hydrogen or substituted or unsubstituted alkyl, aralkyl or cycloalkyl radicals, "alkylene" is an alkylene radical of 1-4 carbons, one Z is halogen and the other Z is halogen or the residue of a hydroxy compound attached via the -O- atom, Q is -CO- or -SO2-, n is 0, 1 or 2, m is an integer of from 1-4, p is an integer of from 1-8, the sum of p and m is less than 9 and the radical A may be further substituted. The dyes are made by condensing a phthalocyanine of the Formula II:- <FORM:1020304/C4-C5/2> with a quinoxaline of Formula III:- <FORM:1020304/C4-C5/3> or by acylating a compound of the formula <FORM:1020304/C4-C5/4> with a quinoxaline of Formula III and condensing the product with a metal phthalocyanine carboxylic or sulphonic acid halide. The specified values for Z are chlorine, bromine, methoxy and esterified hydroxyalkoxy. Substituents in nucleus A may be chloro, methyl, methoxy, methylsulphonyl and nitro and phthalocyanines of copper, nickel and cobalt are specified for Ap. The dyes are reactive for cellulose and also dye wool and synthetic polyamides
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF0039467 | 1963-04-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1020304A true GB1020304A (en) | 1966-02-16 |
Family
ID=7097782
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1447564A Expired GB1020304A (en) | 1963-04-11 | 1964-04-08 | Phthalocyanine dyestuffs |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE646314A (en) |
GB (1) | GB1020304A (en) |
NL (1) | NL6403579A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2038213A1 (en) * | 1969-04-03 | 1971-01-08 | Sandoz Sa | |
US6713613B1 (en) | 1999-05-19 | 2004-03-30 | North Carolina State University | Reactive dye compounds |
US6716969B1 (en) | 1999-05-19 | 2004-04-06 | North Carolina State University | Reactive dye compounds |
US6723834B1 (en) | 1999-10-01 | 2004-04-20 | North Carolina State University | Reactive dye compounds |
US6736864B1 (en) | 1999-10-01 | 2004-05-18 | North Carolina State University | Reactive dye compounds |
US6790943B1 (en) | 1999-10-01 | 2004-09-14 | North Carolina State University | Reactive dye compounds |
US6869453B1 (en) | 1999-10-01 | 2005-03-22 | North Carolina State University | Reactive dye compounds |
-
1964
- 1964-04-03 NL NL6403579A patent/NL6403579A/xx unknown
- 1964-04-08 GB GB1447564A patent/GB1020304A/en not_active Expired
- 1964-04-09 BE BE646314D patent/BE646314A/xx unknown
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2038213A1 (en) * | 1969-04-03 | 1971-01-08 | Sandoz Sa | |
US6713613B1 (en) | 1999-05-19 | 2004-03-30 | North Carolina State University | Reactive dye compounds |
US6716969B1 (en) | 1999-05-19 | 2004-04-06 | North Carolina State University | Reactive dye compounds |
US6723834B1 (en) | 1999-10-01 | 2004-04-20 | North Carolina State University | Reactive dye compounds |
US6736864B1 (en) | 1999-10-01 | 2004-05-18 | North Carolina State University | Reactive dye compounds |
US6790943B1 (en) | 1999-10-01 | 2004-09-14 | North Carolina State University | Reactive dye compounds |
US6869453B1 (en) | 1999-10-01 | 2005-03-22 | North Carolina State University | Reactive dye compounds |
Also Published As
Publication number | Publication date |
---|---|
NL6403579A (en) | 1964-10-12 |
BE646314A (en) | 1964-07-31 |
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