GB191112126A - Process for the Production of Tertiary Trisazodyestuffs. - Google Patents
Process for the Production of Tertiary Trisazodyestuffs.Info
- Publication number
- GB191112126A GB191112126A GB191112126DA GB191112126A GB 191112126 A GB191112126 A GB 191112126A GB 191112126D A GB191112126D A GB 191112126DA GB 191112126 A GB191112126 A GB 191112126A
- Authority
- GB
- United Kingdom
- Prior art keywords
- nitro
- naphthylamine
- phenylenediamine
- sulphonic
- aniline
- 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
- C09B31/16—Trisazo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
12,126. Farbenfabriken vorm. F. Bayer & Co. May 21, 1910, [Convention date]. Samples furnished. Trisazo dyes are obtained by combining a diazosulphonic or diazo carboxylic acid with an amine of the benzene series having a free para-position, rediazotizing, combining the diazoazo compound with a second molecule of the same or a different amine of the benzene series having a free para-position, diazotizing again, and combining with nitro-m-phenylenediamine, nitro-m-toluylenediamine, or 1:3-dioxyquinoline; one of the middle components above-mentioned may be replaced by 1-naphthylamine or its 6- or 7-sulphonic acids; when one of the middle components contains a sulphonic group, a non-sulphonated amine such as aniline may be used as first component. The following combinations are specified : -2-naphthylamine-3:6- disulphonic acid, m-toluidine, m-toluidine, and nitro-m-phenylenediamine; 2-naphthylamine-4: 8-disulphonic acid, alpha-naphthylamine, cresidine, and nitro-m-phenylenediamine; aniline, 1-naphthylamine-7-sulphonic acid, m-toluidine, and nitro - m - phenylenediamine ; aminoazobenzene sulphonic acid, p-xylidine, and nitro-m-phenylenediamine. Other sulphonic or carboxylic acids of the benzene or naphthalene series may be used as first components; aniline, o- or manisidine or their homologues or substitution products may be used as middle components; when aniline is used as middle component, the formaldehyde bisulphite compound or .toluenesulphoanilide is preferably used. The products dye cotton orange to reddish-blue to brown shades. The products with dioxyquinoline as end component have similar properties. Specifications 3673/00, 7292/00, 3654/03, and 5484/08 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE191112126X | 1910-05-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB191112126A true GB191112126A (en) | 1911-12-30 |
Family
ID=34353967
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB191112126D Expired GB191112126A (en) | 1910-05-21 | 1911-05-19 | Process for the Production of Tertiary Trisazodyestuffs. |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB191112126A (en) |
-
1911
- 1911-05-19 GB GB191112126D patent/GB191112126A/en not_active Expired
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