DE127425C - - Google Patents
Info
- Publication number
- DE127425C DE127425C DENDAT127425D DE127425DA DE127425C DE 127425 C DE127425 C DE 127425C DE NDAT127425 D DENDAT127425 D DE NDAT127425D DE 127425D A DE127425D A DE 127425DA DE 127425 C DE127425 C DE 127425C
- Authority
- DE
- Germany
- Prior art keywords
- blue
- amidophenol
- green
- solution
- dye
- 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.)
- Active
Links
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical class Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 9
- 239000000975 dye Substances 0.000 claims description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 3
- 239000011707 mineral Substances 0.000 claims description 3
- 239000003638 reducing agent Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 2
- 238000004040 coloring Methods 0.000 claims 1
- 239000000243 solution Substances 0.000 description 6
- 210000002268 Wool Anatomy 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- HPGGPRDJHPYFRM-UHFFFAOYSA-J Tin(IV) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001844 chromium Chemical class 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 239000001046 green dye Substances 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000004893 oxazines Chemical class 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000005185 salting out Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
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
- C09B19/00—Oxazine dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
KAISERLICHESIMPERIAL
PATENTAMT.PATENT OFFICE.
PATENTSCHRIFTPATENT LETTERING
- JV! 127425 KLASSE 22 c. - JV! 127425 CLASS 22 c.
BADISCHE ANILIN- UND SODA-FABRIK in LUDWIGSHAFEN a. Rh.BADISCHE ANILINE AND SODA FACTORY in LUDWIGSHAFEN a. Rh.
Patentirt im Deutschen Reiche vom 15. August 1899 ab.Patented in the German Empire on August 15, 1899.
Es wurde gefunden, dafs man blaugrüne, vermuthlich der Oxazinklasse angehörige Farbstoffe erhält, wenn man die salzsauren Nitrosoalkyl-m-amidophenole in wässeriger, verdünnt salzsaurer oder verdünnt essigsaurer Lösung bei Gegenwart gewisser Reductionsmittel erhitzt. Die Farbstoffbildung geht sehr rasch (in circa ι Stunde) mit guter Ausbeute vor sich, und die erhaltenen Producte sind von grofser Reinheit.It has been found that blue-green dyes, presumably belonging to the oxazine class, are found obtained when the hydrochloric acid nitrosoalkyl-m-amidophenols heated in aqueous, diluted hydrochloric acid or diluted acetic acid solution in the presence of certain reducing agents. The dye formation goes very quickly (in about 1 hour) with good yield, and the the products obtained are of great purity.
Als Reductionsmittel kann man Zinnchlorür oder Eisenoxydulsalze benutzen; die besten Resultate wurden bisher unter Verwendung des ersteren erhalten.Tin chloride or iron oxide salts can be used as reducing agents; the best Results have so far been obtained using the former.
Die so entstehenden Farbstoffe unterscheiden sich von allen ähnlichen bisher bekannten, und besonders von den aus dem Amidoalkyl-mamidophenol nach Möhlau (Berichte 25, 1066) entstehenden, durch ihr charakteristisches Verhalten gegen Mineralsäuren, wobei sie mit leuchtend grüner Farbe gelöst bezw. als lebhaft grüne Niederschläge gefällt werden.The resulting dyes differ from all similar previously known, and especially from the amidoalkyl-mamidophenol according to Möhlau (Reports 25, 1066) resulting from their characteristic behavior towards mineral acids, whereby they are with bright green color solved respectively. when vivid green rainfall is precipitated.
Des weiteren besitzen sie die Fähigkeit, mit Metallbeizen sehr beständige Lacke zu bilden; sie färben chromgebeizte Wolle und Seide in hervorragend walk- und lichtechten Tönen an. Die Färbungen können auch auf ungeheizter Wolle mit Chromsalzen nachbehandelt werden. Auch zum Färben von chromgebeizter Baumwolle und zum Baumwolldruck können sie, mit Chromsalzen gemischt, benutzt werden.Furthermore, they have the ability to form very stable lacquers with metal stains; they dye chrome-stained wool and silk in excellent mill-fast and lightfast shades. The dyeings can also be treated with chromium salts on unheated wool. They can also be used for dyeing chrome-stained cotton and for cotton printing, mixed with chromium salts, can be used.
Brauchbare Farbstoffe wurden bisher unter Anwendung von:Useful dyes have so far been made using:
Nitrosodimethyl-m-amidophenol,
Nitrosodiäthyl-m-amidophenol und
Nitrosomonoäthyl-m-amidophenol
erhalten.Nitrosodimethyl-m-amidophenol,
Nitrosodiethyl-m-amidophenol and
Nitrosomonoethyl-m-amidophenol
obtain.
12 Theile salzsaures Nitrosodiäthyl-m-amidophenol werden mit 80 Theilen Wasser übergössen, 5 Theile krystallisirtes Zinnchlorür hinzugefügt und unter Rühren circa 1 Stunde in kochendem Wasserbade erhitzt.12 parts of hydrochloric acid nitrosodiethyl-m-amidophenol are poured over with 80 parts of water, 5 parts of crystallized tin chloride are added and, while stirring, for about 1 hour heated in a boiling water bath.
Zur Isolirung des Farbstoffs wird die grüngefärbte Mischung mit verdünnter Salzsäure versetzt und die erhaltene Fällung abfiltrirt. Diese wird dann mit verdünnter kalter Sodalösung angerührt, wobei sie mit tiefblauer Farbe in Lösung geht; aus der filtrirten Lösung wird der Farbstoff durch Zusatz von Kochsalzlösung abgeschieden.To isolate the dye, the green-colored mixture is mixed with dilute hydrochloric acid added and the precipitate obtained is filtered off. This is then diluted with cold soda solution mixed, whereby it goes into solution with deep blue color; from the filtered solution the dye is deposited by adding saline solution.
In ganz ähnlicher Weise verfährt man bei Anwendung des Dimethyl- und des Monoäthylderivates an Stelle des im Beispiel benutzten Nitrosodiäthyl-m-amidophenols; der Farbstoff scheidet sich in ersterem Falle, wenn das Aussalzen warm vorgenommen wird, in grünglänzenden Nädelchen aus.A very similar procedure is followed when using the dimethyl and monoethyl derivatives instead of the nitrosodiethyl-m-amidophenol used in the example; the dye In the first case, if the salting out is carried out warm, it becomes green and shiny Needle off.
Die nachstehende Tabelle giebt die Eigenschaften der entstehenden Producte an:The following table gives the properties of the resulting products:
des Natronsalzes
in Wassersolution
of sodium salt
in water
der wässerigen Lösung
beim Versetzen mit
Mineralsäurencolour
the aqueous solution
when moving with
Mineral acids
chromirte WolleColors
chromed wool
Claims (1)
Publications (1)
Publication Number | Publication Date |
---|---|
DE127425C true DE127425C (en) |
Family
ID=396012
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT127425D Active DE127425C (en) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE127425C (en) |
-
0
- DE DENDAT127425D patent/DE127425C/de active Active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE749073C (en) | Process for producing a tetrakisazo dye | |
DE127425C (en) | ||
DE942104C (en) | Process for the production of metal-containing azo dyes | |
DE677662C (en) | Process for the preparation of o-oxyazo dyes | |
DE455953C (en) | Process for the preparation of monoazo dyes | |
DE77120C (en) | Process for the preparation of blue stain-coloring oxazine dyes ^ | |
DE243491C (en) | ||
DE226002C (en) | ||
DE842090C (en) | Process for the production of on-fiber or in substance chromable azo dyes | |
DE79583C (en) | ||
DE216904C (en) | ||
DE195085C (en) | ||
DE109261C (en) | ||
DE229525C (en) | ||
DE84509C (en) | ||
DE88084C (en) | ||
DE169579C (en) | ||
DE494531C (en) | Process for the preparation of oxynitroso dyes and their metallic lacquers | |
DE66886C (en) | Process for the preparation of indulin-like dyes from azo compounds of benzidine and diamidotriphenylmethane | |
DE65863C (en) | Process for the preparation of a brown azo dye from 1 molecule of toluenediaminesulfonic acid and 1 molecule of m-phenylenediamine | |
DE85390C (en) | ||
DE244652C (en) | ||
DE125581C (en) | ||
DE534931C (en) | Process for the production of wool dyes | |
DE151018C (en) |