GB389758A - Manufacture of dyestuffs - Google Patents
Manufacture of dyestuffsInfo
- Publication number
- GB389758A GB389758A GB27968/32A GB2796832A GB389758A GB 389758 A GB389758 A GB 389758A GB 27968/32 A GB27968/32 A GB 27968/32A GB 2796832 A GB2796832 A GB 2796832A GB 389758 A GB389758 A GB 389758A
- Authority
- GB
- United Kingdom
- Prior art keywords
- class
- dyes
- sulphonic
- chloraniline
- sulphonated
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Azo dyes; cellulose esters or ethers, dyeing.--Azo dyes suitable for dyeing cellulose ester or ether materials are produced in substance by coupling diazotized 4-nitro-2-chloraniline with an N-alkyl-o -sulphonic acid of a non-sulphonated mononuclear primary amine of the benzene series containing no substituent in m-position to the amino group and splitting off the alkyl-o -sulphonic group. The products dye acetate silk pure orange to red orange shades fast to light and washing. They are preferably used in finely subdivided form obtained by grinding to form a paste with water containing a dispersing agent such as a sulphonated residue from the manufacture of benzaldehyde or turpentine (cf. Specification 271,898, [Class 2 (iii), Dyes &c.]. Such pastes may be converted into dry preparations, which can be powdered, by cautious drying in vacuo in presence of a further quantity of the same dispersing agent or another such as sulphite cellulose lye. In an example diazotized 4-nitro-2-chloraniline is coupled in the cold with the sodium salt of the o -methanesulphonic acid of aniline, o-toluidine or o-anisidine and the product is heated with caustic soda solution to split off the methyl-o -sulphonic group. Specifications 11343/99, [Class 2, Acids and salts, Organic &c.], and 200,873, [Class 2 (iii), Dyes &c.], also are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH389758X | 1931-10-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB389758A true GB389758A (en) | 1933-03-23 |
Family
ID=4513906
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB27968/32A Expired GB389758A (en) | 1931-10-12 | 1932-10-07 | Manufacture of dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB389758A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2500080A (en) * | 1945-02-02 | 1950-03-07 | Francolor Sa | Insolubilization of a soluble azoic dyestuff on the fiber |
-
1932
- 1932-10-07 GB GB27968/32A patent/GB389758A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2500080A (en) * | 1945-02-02 | 1950-03-07 | Francolor Sa | Insolubilization of a soluble azoic dyestuff on the fiber |
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