GB191117123A - Manufacture of New Indophenols and of New Sulphur Dyestuffs Derived therefrom. - Google Patents
Manufacture of New Indophenols and of New Sulphur Dyestuffs Derived therefrom.Info
- Publication number
- GB191117123A GB191117123A GB191117123DA GB191117123A GB 191117123 A GB191117123 A GB 191117123A GB 191117123D A GB191117123D A GB 191117123DA GB 191117123 A GB191117123 A GB 191117123A
- Authority
- GB
- United Kingdom
- Prior art keywords
- indophenols
- new
- derivatives
- green
- chlorimide
- 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
- C09B49/00—Sulfur dyes
- C09B49/10—Sulfur dyes from diphenylamines, indamines, or indophenols, e.g. p-aminophenols or leucoindophenols
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
Abstract
17,123. Bloxam, A. G., [Akt.-Ges. f³r Anilin-Fabrikation]. July 26. Indophenols are obtained from those derivatives of 1:8-diaminonaphthalene in which a heteronuclear ring is found by inclusion of a carbon or nitrogen atom, such as perimidine and its derivatives, dihydrothioperimidone, dihydroperimidone, or 1:8-aziminonaphthalene, by oxidation with p-aminophenol or its derivatives, or by condensation with quinone chlorimide or its derivatives. Products are specified from:- 2-methylperimidine and 2:6-dichlor-p-aminophenol; perimidine or 2-phenylperimidine and quinone chlorimide; dihydrothioperimidone or dihydroperimidone and quinone chlorimide or dichlorquinone chlorimide; 1:8-aziminonaphthalene and dichlorquinonechlorimide. Leucoindophenols are obtained by reducing the above-described indophenols. Sulphuretted dyes are obtained by heating the above-described indophenols or leucoindophenols with alkali polysulphide of high or low percentage of sulphur, in the presence or absence of a solvent or diluent. The products dye cotton in sodium sulphide baths green, olive-green, and blackish-green tints.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB191117123T | 1911-07-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB191117123A true GB191117123A (en) | 1912-05-22 |
Family
ID=32565656
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB191117123D Expired GB191117123A (en) | 1911-07-26 | 1911-07-26 | Manufacture of New Indophenols and of New Sulphur Dyestuffs Derived therefrom. |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB191117123A (en) |
-
1911
- 1911-07-26 GB GB191117123D patent/GB191117123A/en not_active Expired
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