GB1361409A - Azo dye-stuffs process for their manufacture and their use - Google Patents
Azo dye-stuffs process for their manufacture and their useInfo
- Publication number
- GB1361409A GB1361409A GB5156271A GB5156271A GB1361409A GB 1361409 A GB1361409 A GB 1361409A GB 5156271 A GB5156271 A GB 5156271A GB 5156271 A GB5156271 A GB 5156271A GB 1361409 A GB1361409 A GB 1361409A
- Authority
- GB
- United Kingdom
- Prior art keywords
- optionally
- optionally substituted
- dyes
- group
- nov
- 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
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 239000000975 dye Substances 0.000 abstract 3
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- 239000000987 azo dye Substances 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 230000008878 coupling Effects 0.000 abstract 1
- 238000010168 coupling process Methods 0.000 abstract 1
- 238000005859 coupling reaction Methods 0.000 abstract 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 abstract 1
- 238000006193 diazotization reaction Methods 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- 125000001841 imino group Chemical group [H]N=* 0.000 abstract 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 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 238000005956 quaternization reaction Methods 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 230000003381 solubilizing effect Effects 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- 125000000147 tetrahydroquinolinyl group Chemical group N1(CCCC2=CC=CC=C12)* 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/02—Disazo 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
- C09B27/00—Preparations in which the azo group is formed in any way other than by diazotising and coupling, e.g. oxidation
-
- 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
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/003—Cyclisation of azo dyes; Condensation of azo dyes with formation of ring, e.g. of azopyrazolone 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
- C09B44/00—Azo dyes containing onium groups
- C09B44/02—Azo dyes containing onium groups containing ammonium groups not directly attached to an azo group
- C09B44/04—Azo dyes containing onium groups containing ammonium groups not directly attached to an azo group from coupling components containing amino as the only directing group
-
- 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
- C09B62/0061—Azodyes with coupling components containing an amino directing group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Coloring (AREA)
- Paper (AREA)
- Pyridine Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1361409 Azo dyes CIBA-GEIGY AG 5 Nov 1971 [6 Nov 1970 4 Oct 1971] 51562/71 Heading C4P The invention comprises azo dyes free from acid water solubilizing groups of formula in which D is the radical of a diazo component; A is an optionally substituted p-phenylene radical; Y is -S-, -O- or an optionally alkylated imino group; R 1 is an optionally substituted alkyl group which together with A may form a tetrahydroquinoline ring; R 2 represents an optionally substituted divalent aliphatic group, optionally containing a chain-oxygen atom and R 4 is an optionally substituted aliphatic hydrocarbyl group and ring B, which may be aromatic or partially or wholly saturated, may be substituted by halogen atoms, nitro groups and organic radicals. The dyes may be obtained by diazotization and coupling followed optionally by quaternization of any introgen atoms in the residue D. The dyes may be used alone or in admixture, optionally with a different monoazo dye.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1647370A CH544137A (en) | 1970-11-06 | 1970-11-06 | Water-insol mono-azo dyes - contg benzothiazole benzoxazole or benzimidazole gps for dyeing wool,silk,leather and synthetic fibre |
| CH1446171A CH567066A5 (en) | 1971-10-04 | 1971-10-04 | Water-insol mono-azo dyes - contg benzothiazole benzoxazole or benzimidazole gps for dyeing wool,silk,leather and synthetic fibre |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1361409A true GB1361409A (en) | 1974-07-24 |
Family
ID=25714503
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5156271A Expired GB1361409A (en) | 1970-11-06 | 1971-11-05 | Azo dye-stuffs process for their manufacture and their use |
| GB4044072A Expired GB1361410A (en) | 1970-11-06 | 1971-11-05 | Benzthiazole-oxazole and -imidazole coupling agents |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4044072A Expired GB1361410A (en) | 1970-11-06 | 1971-11-05 | Benzthiazole-oxazole and -imidazole coupling agents |
Country Status (8)
| Country | Link |
|---|---|
| BE (1) | BE774960A (en) |
| DE (1) | DE2154477A1 (en) |
| ES (1) | ES396690A1 (en) |
| FR (1) | FR2116386B1 (en) |
| GB (2) | GB1361409A (en) |
| IT (1) | IT942277B (en) |
| NL (1) | NL7115287A (en) |
| PL (1) | PL81411B1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6787570B2 (en) | 1999-09-23 | 2004-09-07 | Pfizer, Inc. | Substituted N-cycloalkyl-N-benzyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA994761A (en) * | 1972-05-12 | 1976-08-10 | Max A. Weaver | Azo compounds and polyamide materials dyed therewith |
-
1971
- 1971-11-02 DE DE19712154477 patent/DE2154477A1/en active Pending
- 1971-11-04 PL PL15145271A patent/PL81411B1/en unknown
- 1971-11-04 FR FR7139531A patent/FR2116386B1/fr not_active Expired
- 1971-11-05 BE BE774960A patent/BE774960A/en unknown
- 1971-11-05 ES ES396690A patent/ES396690A1/en not_active Expired
- 1971-11-05 IT IT5387771A patent/IT942277B/en active
- 1971-11-05 GB GB5156271A patent/GB1361409A/en not_active Expired
- 1971-11-05 GB GB4044072A patent/GB1361410A/en not_active Expired
- 1971-11-05 NL NL7115287A patent/NL7115287A/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6787570B2 (en) | 1999-09-23 | 2004-09-07 | Pfizer, Inc. | Substituted N-cycloalkyl-N-benzyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1361410A (en) | 1974-07-24 |
| DE2154477A1 (en) | 1972-05-10 |
| IT942277B (en) | 1973-03-20 |
| FR2116386B1 (en) | 1975-07-18 |
| NL7115287A (en) | 1972-05-09 |
| FR2116386A1 (en) | 1972-07-13 |
| ES396690A1 (en) | 1974-11-16 |
| BE774960A (en) | 1972-05-05 |
| PL81411B1 (en) | 1975-08-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |