AT49561B - Process for the preparation of dianthraquinonyl or polyanthraquinonyl ureas. - Google Patents
Process for the preparation of dianthraquinonyl or polyanthraquinonyl ureas.Info
- Publication number
- AT49561B AT49561B AT49561DA AT49561B AT 49561 B AT49561 B AT 49561B AT 49561D A AT49561D A AT 49561DA AT 49561 B AT49561 B AT 49561B
- Authority
- AT
- Austria
- Prior art keywords
- dianthraquinonyl
- preparation
- polyanthraquinonyl
- ureas
- diaminoanthraquinones
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 2
- 235000013877 carbamide Nutrition 0.000 title 1
- 150000003672 ureas Chemical class 0.000 title 1
- LRMDXTVKVHKWEK-UHFFFAOYSA-N 1,2-diaminoanthracene-9,10-dione Chemical class C1=CC=C2C(=O)C3=C(N)C(N)=CC=C3C(=O)C2=C1 LRMDXTVKVHKWEK-UHFFFAOYSA-N 0.000 claims description 2
- 230000004048 modification Effects 0.000 claims 1
- 238000012986 modification Methods 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000001043 yellow dye Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<Desc/Clms Page number 1>
EMI1.1
EMI1.2
<Desc/Clms Page number 2>
Der hiebei erhaltono gelbe Farbstoff löst sich in konzentrierter Schwefelsäure mit gelbroter Farbe und färbt Baumwolle und Wolle in orangegelben Tönen an. Denselben Farbstoff erzielt man durch Erhitzen von 2 Mol. ss-Anthrachinonylharnstoffchlorid mit 1 Mol.
2 : 6/2 : 7-Diaminoanthrachinon.
<Desc / Clms Page number 1>
EMI1.1
EMI1.2
<Desc / Clms Page number 2>
The yellow dye obtained here dissolves in concentrated sulfuric acid with a yellow-red color and stains cotton and wool in orange-yellow tones. The same dye is obtained by heating 2 moles of ß-anthraquinonylurea chloride with 1 mole.
2: 6/2: 7 diaminoanthraquinone.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE47522X | 1909-02-01 | ||
| DE49561X | 1909-02-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT49561B true AT49561B (en) | 1911-08-25 |
Family
ID=25749052
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT49561D AT49561B (en) | 1909-02-01 | 1910-02-07 | Process for the preparation of dianthraquinonyl or polyanthraquinonyl ureas. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT49561B (en) |
-
1910
- 1910-02-07 AT AT49561D patent/AT49561B/en active
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