GB1111463A - 1:2 chromium complexes of a reactive disazo dye and a monoazo dye and their use - Google Patents
1:2 chromium complexes of a reactive disazo dye and a monoazo dye and their useInfo
- Publication number
- GB1111463A GB1111463A GB1485166A GB1485166A GB1111463A GB 1111463 A GB1111463 A GB 1111463A GB 1485166 A GB1485166 A GB 1485166A GB 1485166 A GB1485166 A GB 1485166A GB 1111463 A GB1111463 A GB 1111463A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- dye
- benzene
- reacting
- complex
- 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
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 title abstract 2
- 150000001844 chromium Chemical class 0.000 title 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 title 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 8
- 239000011651 chromium Substances 0.000 abstract 4
- 239000000975 dye Substances 0.000 abstract 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical group C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 abstract 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 abstract 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical group C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 abstract 1
- 229920002678 cellulose Polymers 0.000 abstract 1
- 239000001913 cellulose Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 229910052804 chromium Inorganic materials 0.000 abstract 1
- 239000002657 fibrous material Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 150000002790 naphthalenes Chemical class 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
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
- C09B62/022—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 the heterocyclic ring being alternatively specified
- C09B62/026—Azo dyes
- C09B62/032—Metal complex azo dyes
-
- 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
- C09B62/002—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the linkage of the reactive group being alternatively specified
- C09B62/006—Azodyes
- C09B62/012—Metal complex azo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
The invention comprises chromium containing reactive dyestuffs of the formula <FORM:1111463/C4-C5/1> wherein A1 represents a benzene or naphthalene residue containing no reactive groups, B represents a benzene, naphthalene or pyrazole residue containing no reactive groups, each of A1 and B containing the -0- in a position adjacent to -N=N-, n is a positive whole number of at most 3, A2 represents an unsulphonated radical of the benzene or naphthalene series containing no reactive groups, and Z represents a monocyclic or dicyclic radical which comprises a 5- or 6- membered heterocyclic ring of aromatic character having at least one grouping <FORM:1111463/C4-C5/2> halogen as a portion of said heterocyclic ring. They may be obtained either by reacting a complex Cr compound of the formula <FORM:1111463/C4-C5/3> with a metallizable disazo dyestuff of the formula <FORM:1111463/C4-C5/4> or by reacting a Cr complex of the formula <FORM:1111463/C4-C5/5> with an acylating agent introducing the radical Z. Specified heterocyclic rings present in Z are triazine, pyrimidine, quinoxaline and benzthiazole rings. The dyes may be used to dye or print cellulose or polyamide fibrous material brown-black to green-black shades. The starting material of Formula IV may be obtained by reacting a complex Cr compound of Formula I with an aminodisazo dyestuff of formula <FORM:1111463/C4-C5/6> Reference has been directed by the Comptroller to Specification 851,861.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH470765A CH472477A (en) | 1963-10-07 | 1965-04-05 | Process for the production of chromium-containing reactive dyes |
| CH1816368A CH472479A (en) | 1963-10-07 | 1965-04-05 | Process for the production of chromium-containing reactive dyes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1111463A true GB1111463A (en) | 1968-04-24 |
Family
ID=25696114
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1485166A Expired GB1111463A (en) | 1965-04-05 | 1966-04-04 | 1:2 chromium complexes of a reactive disazo dye and a monoazo dye and their use |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1111463A (en) |
-
1966
- 1966-04-04 GB GB1485166A patent/GB1111463A/en not_active Expired
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