AT48689B - Process for the preparation of a water- and oil-insoluble disazo dye. - Google Patents
Process for the preparation of a water- and oil-insoluble disazo dye.Info
- Publication number
- AT48689B AT48689B AT48689DA AT48689B AT 48689 B AT48689 B AT 48689B AT 48689D A AT48689D A AT 48689DA AT 48689 B AT48689 B AT 48689B
- Authority
- AT
- Austria
- Prior art keywords
- water
- oil
- preparation
- disazo dye
- insoluble disazo
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
<Desc/Clms Page number 1>
Verfahren zur Darstellung eines wasser- und ölunlöslichen Disazofarbstoffes.
Lässt man auf die Diazethylverbindung des m-m'-Dichlorbenzidin (NH2 : Cl = 1 : 3) die zwei Molekülen entsprechende Menge Salpetersäure einwirken, so erhält man nach der Verseifung des Reaktionsproduktes ein Dichlordinitrobenzidin, welchem wahrscheinlich die Konstitution :
EMI1.1
zukommt.
Es wurde nun gefunden, dass die Tetrazoverbindung dieses Dichtordinitrobenzidin bei der Kombination mit 2 Molekülen ss-Naphtol einen roten Disazofarbstoff liefert, welcher wegen seiner Wasserunlöslichkeit und hervorragenden Olechtheit der Darstellung von
EMI1.2
hervorragend ölechten Disazofarbstoff liefern würde.
Darstellung des Dichlordinitrobenzidin : m-m'-Dichlorbenzidin wird in üblicher Weise in die Diazethylverbindung übergeführt,
EMI1.3
ungefähr 2550 C.
Darstellung dos Farbstoffes : 34 3 Tei) o Dichlordinitrobenzidin werden mit 200 Teilen Wasser und HO Teilen
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<Desc/Clms Page number 2>
140 Teile Natriumazetat zugefügt waren, einfliessen. Der Farbstoff bildet'sich rasch und scheidet sich in roten Flocken airs. Er wird abfiltriort, mit Wasser gewaschen und vorteil- haft in Pastenform verwendet.
EMI2.1
oder Harxteim, zugesetzt worden oder es kann die Kombination bei Abwesenheit eines dieser Stoffe ausgeführt werden. Selbstvorständlich kann man die Kupplung der Tetr8O- verbindung mit -Naphtol auch bei Gegenwart eines Substrates vornehmen.
<Desc / Clms Page number 1>
Process for the preparation of a water- and oil-insoluble disazo dye.
If the diazethyl compound of m-m'-dichlorobenzidine (NH2: Cl = 1: 3) is allowed to act in the amount of nitric acid corresponding to two molecules, a dichlorodonitrobenzidine is obtained after saponification of the reaction product, which probably has the constitution:
EMI1.1
comes to.
It has now been found that the tetrazo compound of this dense-ordinitrobenzidine, when combined with 2 molecules of ss-naphtol, produces a red disazo dye which, because of its insolubility in water and excellent weakness of the representation of
EMI1.2
would provide excellent oleic disazo dye.
Preparation of the dichloroditrobenzidine: m-m'-dichlorobenzidine is converted into the diazethyl compound in the usual way,
EMI1.3
about 2550 C.
Presentation of the dye: 34 3 parts dichlorodinitrobenzidine are mixed with 200 parts of water and HO parts
EMI1.4
<Desc / Clms Page number 2>
140 parts of sodium acetate were added, flow in. The dye forms rapidly and separates in red flakes. It is filtered off, washed with water and advantageously used in paste form.
EMI2.1
or Harxteim, has been added, or the combination can be carried out in the absence of one of these substances. Of course, the coupling of the Tetr8O compound with -naphtol can also be carried out in the presence of a substrate.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE48689X | 1910-02-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
AT48689B true AT48689B (en) | 1911-06-26 |
Family
ID=5626070
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT48689D AT48689B (en) | 1910-02-10 | 1910-07-04 | Process for the preparation of a water- and oil-insoluble disazo dye. |
Country Status (1)
Country | Link |
---|---|
AT (1) | AT48689B (en) |
-
1910
- 1910-07-04 AT AT48689D patent/AT48689B/en active
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