GB462629A - Manufacture of dyestuffs - Google Patents
Manufacture of dyestuffsInfo
- Publication number
- GB462629A GB462629A GB5910/36A GB591036A GB462629A GB 462629 A GB462629 A GB 462629A GB 5910/36 A GB5910/36 A GB 5910/36A GB 591036 A GB591036 A GB 591036A GB 462629 A GB462629 A GB 462629A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- amino
- sulphone
- nitrophenyl
- wool
- 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
- C09B29/24—Monoazo dyes prepared by diazotising and coupling from coupling components containing both hydroxyl and amino directing groups
- C09B29/28—Amino naphthols
- C09B29/30—Amino naphtholsulfonic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Azo dyes; acid wool dyes without mordants, dyeing with.--Azo dyestuffs are manufactured by coupling a diazo-compound with an aldehyde bisulphite compound of 2-amino-8-naphthol-6-sulphonic acid in alkaline, neutral or acid medium. Suitable diazo components are aniline, toluidines, anisidines and sulphonic acids thereof, their substitution products containing a nitro-group in p-position to the amino-group, and particularly compounds nitrated in p-position to the amino-group and containing in o-position a sulphone-alkyl or -aralkyl group, e.g. 1-amino-4-nitrophenyl-2-methyl, -ethyl or benzyl sulphone, or substitution products thereof, e.g. those containing halogen, alkyl, alkoxy or nitro-groups. The products dye animal fibres, e.g. wool and silk, advantageously in the presence of sulphuric acid or of capillary active substances containing in their kation a basic nitrogen atom and an aliphatic or araliphatic residue of more than 8 carbon atoms. Examples describe the manufacture of the following dyestuffs: (1) 1-amino-4-nitrophenyl-2-methyl sulphone --> the sodium salt of the formaldehyde bisulphite compound of 2 : 8 : 6-acid; the product dyes wool or silk in an acid bath blue shades; (2) 1-amino-4-nitrophenyl-2-benzyl sulphone --> the same coupling component or the corresponding potassium or other salt (somewhat more greenish-blue shades); the diazo-component may be replaced by the 2-ethyl sulphone, by nitrated amines such as p-nitraniline or p-nitro-o-chloraniline (violet shades), by p - nitraniline - o - sulphonic acid (reddish-blue shades), or by simpler amines such as aniline, sulphanilic acid, naphthionic acid or monobenzoyl - p - phenylenediamine (orange to red); the coupling component may be replaced by the corresponding acetaldehyde or furfural bisulphite compound. In example (3), wool is dyed blue with the product of (1) from a bath containing sodium sulphate and sulphuric acid. Specifications 11343/99, [Class 2], 433,230, 436,790, 436,863, 439,890, and 451,970 are referred to. Aldehyde bisulphite compounds of 2 : 8 : 6-acid are manufactured by reacting the acid or a salt thereof with an aldehyde bisulphite compound. 1-Amino-4-nitrophenyl-2-methyl, -ethyl and benzyl sulphones are obtainable by reacting sodium 1 - chloro - 4 - nitrobenzene - 2 - sulphinate with methyl bromide, ethyl bromide or benzyl chloride respectively, and heating the products with aqueous ammonia under pressure.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH462629X | 1935-02-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB462629A true GB462629A (en) | 1937-03-12 |
Family
ID=4515767
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5910/36A Expired GB462629A (en) | 1935-02-28 | 1936-02-27 | Manufacture of dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB462629A (en) |
-
1936
- 1936-02-27 GB GB5910/36A patent/GB462629A/en not_active Expired
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