GB287609A - Improvements in or relating to the dyeing of regenerated cellulose materials - Google Patents
Improvements in or relating to the dyeing of regenerated cellulose materialsInfo
- Publication number
- GB287609A GB287609A GB3139826A GB3139826A GB287609A GB 287609 A GB287609 A GB 287609A GB 3139826 A GB3139826 A GB 3139826A GB 3139826 A GB3139826 A GB 3139826A GB 287609 A GB287609 A GB 287609A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- dyestuffs
- sulphonic
- cresolmethylether
- amino
- 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)
Abstract
287,609. British Dyestuffs Corporation, Ltd., and Baddiley, J. Dec. 10, 1926. Addition to 283,319. Seconda.ry disazo dyes.-The secondary disazo dyes, other than those used in the parent Specifification, obtained by coupling the diazo compound of a sulphonated or carboxylated p-nitroarylamine with one of the usual middle components, rediazotizing, and coupling with an aminonaphthol sulphonic acid or an N-derivative thereof (except the 2 : 8-aminonaphthol sulphonic acids and their derivatives) are used for dyeing regenerated cellulose materials, e.g. viscose silk, in level shades. The dyestuffs obtained by reduction of the nitro group may also be used, the latter being diazotized on the fibre, if desired, and developed with the usual developers. The shades obtained on viscose silk with dyestuffs from the following components, the end component being coupled alkaline, are tabulated :-p-nitraniline-o-sulphonic acid, m-amino-p-cresolmethylether, and H-acid, acetyl-H-acid, glycine of 2: 5 : 7-acid, 1 : 8 : 4- acid, or 1 : 8-aminonaphthol-2 : 4-disulphonic acid ; p-nitraniline-o-sulphonic acid, m-toluidine, p-xylidine or Cleves acid, and 1 : 8 : 4-acid ; 5- nitro-2-aminobenzoic acid or 2 : 4-dinitraniline-6- sulphonic acid, m-amino-p-cresolmethylether, and 1 : 8 : 4-acid; and the reduced dyestuffs from pnitraniline-o-sulphonic acid: m-amino-p-cresolmethylether and H-a,cid or 1 : 8 : 4-acid. Specifications 19743/92, 4767/09. 4768/09, 11364/09, and 23992/09 are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3139826A GB287609A (en) | 1926-12-10 | 1926-12-10 | Improvements in or relating to the dyeing of regenerated cellulose materials |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3139826A GB287609A (en) | 1926-12-10 | 1926-12-10 | Improvements in or relating to the dyeing of regenerated cellulose materials |
GB3139926A GB283319A (en) | 1926-12-10 | 1926-12-10 | Improvements in the application of azo dyes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB287609A true GB287609A (en) | 1928-03-12 |
Family
ID=26260887
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3139826A Expired GB287609A (en) | 1926-12-10 | 1926-12-10 | Improvements in or relating to the dyeing of regenerated cellulose materials |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB287609A (en) |
-
1926
- 1926-12-10 GB GB3139826A patent/GB287609A/en not_active Expired
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