GB312330A - - Google Patents
Info
- Publication number
- GB312330A GB312330A GB16093/29A GB1609329A GB312330A GB 312330 A GB312330 A GB 312330A GB 16093/29 A GB16093/29 A GB 16093/29A GB 1609329 A GB1609329 A GB 1609329A GB 312330 A GB312330 A GB 312330A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- acids
- monoazo
- dyes
- dyestuff
- 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
- 239000000975 dye Substances 0.000 abstract 10
- 239000002253 acid Substances 0.000 abstract 7
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 6
- 238000004043 dyeing Methods 0.000 abstract 5
- 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 4
- 210000002268 wool Anatomy 0.000 abstract 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 3
- 150000007513 acids Chemical class 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 235000011149 sulphuric acid Nutrition 0.000 abstract 3
- 239000001117 sulphuric acid Substances 0.000 abstract 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
- 241000974482 Aricia saepiolus Species 0.000 abstract 2
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 abstract 2
- 150000005207 1,3-dihydroxybenzenes Chemical class 0.000 abstract 1
- BYYUJKBBBSJVTL-UHFFFAOYSA-N 2-aminooxy-2-methyl-3-oxo-3-phenylpropanoic acid Chemical class NOC(C(=O)O)(C)C(C1=CC=CC=C1)=O BYYUJKBBBSJVTL-UHFFFAOYSA-N 0.000 abstract 1
- DZBPBQLHKGMMOJ-UHFFFAOYSA-N 2-benzoyl-3-(diethylaminooxy)benzoic acid Chemical compound C(C)N(OC=1C(=C(C(=O)O)C=CC1)C(C1=CC=CC=C1)=O)CC DZBPBQLHKGMMOJ-UHFFFAOYSA-N 0.000 abstract 1
- JMEQDCKZJGYAEP-UHFFFAOYSA-N 2-benzoyl-3-(dimethylaminooxy)benzoic acid Chemical compound CN(OC=1C(=C(C(=O)O)C=CC1)C(C1=CC=CC=C1)=O)C JMEQDCKZJGYAEP-UHFFFAOYSA-N 0.000 abstract 1
- FGTYTUFKXYPTML-UHFFFAOYSA-N 2-benzoylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)C1=CC=CC=C1 FGTYTUFKXYPTML-UHFFFAOYSA-N 0.000 abstract 1
- DQSCKJGJALPIOD-UHFFFAOYSA-N 3-aminooxy-2-benzoylbenzoic acid Chemical class NOC=1C(=C(C(=O)O)C=CC1)C(C1=CC=CC=C1)=O DQSCKJGJALPIOD-UHFFFAOYSA-N 0.000 abstract 1
- LHYQAEFVHIZFLR-UHFFFAOYSA-L 4-(4-diazonio-3-methoxyphenyl)-2-methoxybenzenediazonium;dichloride Chemical compound [Cl-].[Cl-].C1=C([N+]#N)C(OC)=CC(C=2C=C(OC)C([N+]#N)=CC=2)=C1 LHYQAEFVHIZFLR-UHFFFAOYSA-L 0.000 abstract 1
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 abstract 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- OXMVLGLNXOXNTF-UHFFFAOYSA-N chloro(phenyl)sulfamic acid Chemical compound OS(=O)(=O)N(Cl)C1=CC=CC=C1 OXMVLGLNXOXNTF-UHFFFAOYSA-N 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
- -1 dimethylaminooxy Chemical group 0.000 abstract 1
- 239000000835 fiber Substances 0.000 abstract 1
- 238000007689 inspection Methods 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 150000005002 naphthylamines Chemical class 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229950000244 sulfanilic acid Drugs 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
- C09B43/00—Preparation of azo dyes from other azo compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE312330T | 1928-05-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB312330A true GB312330A (enrdf_load_stackoverflow) | 1930-08-07 |
Family
ID=31894625
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB16093/29A Expired GB312330A (enrdf_load_stackoverflow) | 1928-05-24 | 1929-05-24 |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB312330A (enrdf_load_stackoverflow) |
-
1929
- 1929-05-24 GB GB16093/29A patent/GB312330A/en not_active Expired
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