GB190904768A - Manufacture and Production of New Azodyestuffs. - Google Patents
Manufacture and Production of New Azodyestuffs.Info
- Publication number
- GB190904768A GB190904768A GB190904768DA GB190904768A GB 190904768 A GB190904768 A GB 190904768A GB 190904768D A GB190904768D A GB 190904768DA GB 190904768 A GB190904768 A GB 190904768A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- sulphonic
- benzoyl
- xylidine
- acetyl
- 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
- 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
- C09B31/08—Disazo dyes from a coupling component "C" containing directive hydroxyl and amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Photoreceptors In Electrophotography (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
4768. Newton, P. A., [Farbenfabriken vorm. F. Bayer & Co.]. Feb. 26. Samples furnished. Secondary disazo dyes are obtained by combining diazotized p-aminoazo compounds wherein the azo and amino groups are linked to the same benzene or naphthalene ring (except those derived from 1 : 8-aminonaphthol or its sulphonic acids) with 2-acidylamino-5-naphthol-7-sulphonic or -1 : 7-disulphonic acid. The following components are specified :-aminoazobenzene sulpbonic acid and 2 - benzoylamino - 5 - naphthol - 7 - sulphonic acid ; aminoazobenzene and 2-ethylurethane-5-naphthol- 1 : 7 - disulphonic acid ; m - aminobenzoic acid, aniline, and 2-benzoylamino-5-naphthol-7-sulphonic acid ; m-aminobenzoic acid, p-xylidine, and acetyl- 2 : 5 : 7-acid ; o-aminobenzene sulphonic acid, mtoluidine, and acetyl- or benzoyl-2 : 5 : 7-acid ; o-aminobenzene sulphonic acid, p - xylidine, and acetyl- or benzoyl-2 : 5 : 7-acid or 2-ethylurethane- 5-naphthol-1 : 7-disulphonic acid ; m-aminobenzene sulpbonic acid, aniline, and 2-methylurethane-5- naphthol-7-sulphonic acid ; m-aminobenzene sulphonic acid, p-xylidine and benzoyl-2 : 5 : 7- or - 2 : 5 : 1 : 7-acid ; sulphanilic acid, aniline, and 2-phenylurethane-5-naphthol-7-sulphonic acid or benzoyl-2 : 5 : 7-acid, aminoazobenzene disulphonic acid and benzoyl-2 : 5 : 7-acid ; 1 : 3 : 4 : 6-xylidine sulphonic acid, cresidine, and acetyl-2 : 5 : 7 acid ; p-chloraniline-o-sulphonic acid, o - toluidine, and 2-phenylurea-5-naphthol-7-sulphonic acid ; p-chloraniline-o-sulphonic acid, m-toluidine, and acetyl- or benzoyl-2 : 5 : 7-acid ; p-chloraniline - o - sulphonic acid, aniline, and m-aminobenzoyl-2 : 5 : 7-acid ; p-nitraniline-m-sulphonic acid, p - xylidine, and benzoyl- or ethylurethane-2 : 5 : 7-acid ; p-nitraniline-m-sulphonic acid, cresidine, and benzoyl- 2 : 5 : 7-acid ; o-nitraniline-p-sulphonic acid, pxylidine, and benzoyl-2 : 5 : 7-acid ; 1-naphthylamine-2 : 5-disulphonic acid, 1-naphthylamine, and benzoyl-2 : 5 : 7-acid ; 1 - naphthylamine - 3 : 6- disulpbonic acid, 1-naphthylamine, and urea-2 : 5 : 7- acid ; 2-naphthylamine-1 : 6- or -3 : 6-disulphonic acid, 1-naphthylamine, and benzoyl-2 : 5 : 7-acid ; 2-naphthylamine-4 : 8-disulphonic acid, p-xylidine, and benzoyl-2 : 5 : 7-acid ; 1 : 5-aminonaphthol-7- sulphonic acid, p-xylidine, and acetyl-2 : 5 : 7-acid ; 1 : 5-aminonaphthol-2 : 7-disulphonic acid, p-xylidine, and acetyl- or benzoyl-2 : 5 : 7-acid : 2 : 5 : 7- acid, p-xylidine, and acetyl-2 :5 :7-acid ; 2 : 5 : 1 :7- acid, p-xylidine and benzoyl-2 : 5 : 7-acid ; p-chloraniline-o-sulphonic acid. p-xylidine, and acetyl- 2 : 5 : 7-acid. The products dye cotton red to blue shades.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB190904768T | 1909-02-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB190904768A true GB190904768A (en) | 1910-01-13 |
Family
ID=32490438
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB190904768D Expired GB190904768A (en) | 1909-02-26 | 1909-02-26 | Manufacture and Production of New Azodyestuffs. |
GB191100316D Expired GB191100316A (en) | 1909-02-26 | 1911-01-05 | A New Azodyestuff. |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB191100316D Expired GB191100316A (en) | 1909-02-26 | 1911-01-05 | A New Azodyestuff. |
Country Status (1)
Country | Link |
---|---|
GB (2) | GB190904768A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5554738A (en) * | 1987-04-27 | 1996-09-10 | Ciba-Geigy Corporation | Acyl-aryl disazo having a 6-ureido-1-hydroxy-naphthalene-3-sulfonic acid coupling component |
-
1909
- 1909-02-26 GB GB190904768D patent/GB190904768A/en not_active Expired
-
1911
- 1911-01-05 GB GB191100316D patent/GB191100316A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5554738A (en) * | 1987-04-27 | 1996-09-10 | Ciba-Geigy Corporation | Acyl-aryl disazo having a 6-ureido-1-hydroxy-naphthalene-3-sulfonic acid coupling component |
Also Published As
Publication number | Publication date |
---|---|
GB191100316A (en) | 1911-12-21 |
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