AT49485B - Process for the preparation of vat-coloring arylaminoanthraquinones. - Google Patents
Process for the preparation of vat-coloring arylaminoanthraquinones.Info
- Publication number
- AT49485B AT49485B AT49485DA AT49485B AT 49485 B AT49485 B AT 49485B AT 49485D A AT49485D A AT 49485DA AT 49485 B AT49485 B AT 49485B
- Authority
- AT
- Austria
- Prior art keywords
- sep
- violet
- arylaminoanthraquinones
- vat
- coloring
- Prior art date
Links
- 238000004040 coloring Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 3
- 150000004056 anthraquinones Chemical class 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 description 2
- 240000007817 Olea europaea Species 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- NNBFNNNWANBMTI-UHFFFAOYSA-M brilliant green Chemical compound OS([O-])(=O)=O.C1=CC(N(CC)CC)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](CC)CC)C=C1 NNBFNNNWANBMTI-UHFFFAOYSA-M 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000010959 steel 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
EMI1.3
EMI1.4
<Desc/Clms Page number 2>
EMI2.1
EMI2.2
<tb>
<tb> Lösung <SEP> in
<tb> Farbstoff <SEP> aus <SEP> Aussehen <SEP> Ausfärbung
<tb> Pyridin <SEP> konz.
<tb>
(Chinolin) <SEP> Schwefelsäure <SEP> Oleum <SEP> (20%)
<tb> braune
<tb> 4.41-Dichlordiphenyl <SEP> + <SEP> bronzierende <SEP> blaustichig <SEP> aufangs <SEP> grün,
<tb> 1. <SEP> + <SEP> 1-Aminoanthrachinon <SEP> Prismen <SEP> rot <SEP> gelb <SEP> daun <SEP> blau <SEP> violett
<tb> 4.41-Dibromdiphenyl <SEP> # <SEP> Mono- <SEP> dunkelblaue
<tb> 2. <SEP> benzoyl-1.4-diaminoanthra- <SEP> Prismen <SEP> blau <SEP> graubraun <SEP> oliv <SEP> blaugrün
<tb> chinon
<tb> 4.41-Dichlor-3.31-dimethyl- <SEP> violett- <SEP> gelbbraun,
<tb> 3. <SEP> diphenyl <SEP> + <SEP> 1-Amino-2-mehtyl- <SEP> braunes <SEP> violettrot <SEP> gelbbraun <SEP> dann <SEP> violett- <SEP> violett
<tb> Anthrachinon <SEP> Kristallmehl <SEP> rot
<tb> 3.31-Dichlordiphenyl <SEP> # <SEP> Mono- <SEP> stahlblaue
<tb> 4.
<SEP> benzoyl-1.4-diamino-Anthra- <SEP> Nadeln <SEP> violett <SEP> oliv <SEP> dunkelgrün <SEP> blau
<tb> chinon
<tb> rotbraune
<tb> 4.41-Dichlordiphenyl-sulfon- <SEP> bronze- <SEP> smaragdgrün,
<tb> 5. <SEP> -1-aminoanthrachinon <SEP> glänzende <SEP> (braunrot) <SEP> grün <SEP> dann <SEP> blau <SEP> braunrot
<tb> Blättchen
<tb> 4.41-Dichlordiphenyl-sulfon <SEP> # <SEP> violette <SEP> schmutzig <SEP> schmutzig
<tb> 6. <SEP> # <SEP> Monobenzoyl-1.4-Diamino- <SEP> Prismen <SEP> (violettblau) <SEP> grün <SEP> grün <SEP> stumpf <SEP> grün
<tb> anthrachinon
<tb> 3.31-Dichlordiphenyl-sulfon <SEP> # <SEP> braunrote <SEP> smaragdg <SEP> ün.
<tb> <SEP>
7. <SEP> # <SEP> 1-Aminoanthrachinon <SEP> Nadeln <SEP> ora@gerot <SEP> grün <SEP> dann <SEP> blau <SEP> rot
<tb> 3.31-Dichlordiphenyl-sulfon <SEP> # <SEP> violettes
<tb> 8. <SEP> - <SEP> Monobenzoyl-1.4-Diamino- <SEP> Kristallmehl <SEP> violett <SEP> grasgrün <SEP> grün <SEP> violett
<tb> anthrachinon
<tb>
**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.
<Desc / Clms Page number 1>
EMI1.1
EMI1.2
EMI1.3
EMI1.4
<Desc / Clms Page number 2>
EMI2.1
EMI2.2
<tb>
<tb> Solution <SEP> in
<tb> Dye <SEP> from <SEP> Appearance <SEP> Color
<tb> pyridine <SEP> conc.
<tb>
(Quinoline) <SEP> sulfuric acid <SEP> oleum <SEP> (20%)
<tb> brown
<tb> 4.41-dichlorodiphenyl <SEP> + <SEP> bronzing <SEP> bluish tint <SEP> on top <SEP> green,
<tb> 1. <SEP> + <SEP> 1-aminoanthraquinone <SEP> prisms <SEP> red <SEP> yellow <SEP> daun <SEP> blue <SEP> violet
<tb> 4.41-Dibromodiphenyl <SEP> # <SEP> Mono- <SEP> dark blue
<tb> 2. <SEP> benzoyl-1.4-diaminoanthra- <SEP> prisms <SEP> blue <SEP> gray-brown <SEP> olive <SEP> blue-green
<tb> chinone
<tb> 4.41-dichloro-3.31-dimethyl- <SEP> violet- <SEP> yellow-brown,
<tb> 3. <SEP> diphenyl <SEP> + <SEP> 1-amino-2-mehtyl- <SEP> brown <SEP> violet-red <SEP> yellow-brown <SEP> then <SEP> violet- <SEP> violet
<tb> Anthraquinone <SEP> crystal powder <SEP> red
<tb> 3.31-dichlorodiphenyl <SEP> # <SEP> Mono- <SEP> steel blue
<tb> 4.
<SEP> benzoyl-1.4-diamino-anthra- <SEP> needles <SEP> violet <SEP> olive <SEP> dark green <SEP> blue
<tb> chinone
<tb> red-brown
<tb> 4.41-dichlorodiphenyl-sulfone- <SEP> bronze- <SEP> emerald green,
<tb> 5. <SEP> -1-aminoanthraquinone <SEP> shiny <SEP> (brown-red) <SEP> green <SEP> then <SEP> blue <SEP> brown-red
<tb> leaflets
<tb> 4.41-dichlorodiphenyl-sulfone <SEP> # <SEP> violet <SEP> dirty <SEP> dirty
<tb> 6. <SEP> # <SEP> Monobenzoyl-1.4-Diamino- <SEP> prisms <SEP> (violet blue) <SEP> green <SEP> green <SEP> blunt <SEP> green
<tb> anthraquinone
<tb> 3.31-dichlorodiphenyl-sulfone <SEP> # <SEP> brown-red <SEP> emeraldg <SEP> ün.
<tb> <SEP>
7. <SEP> # <SEP> 1-aminoanthraquinone <SEP> needles <SEP> ora @ gerot <SEP> green <SEP> then <SEP> blue <SEP> red
<tb> 3.31-Dichlorodiphenyl-sulfone <SEP> # <SEP> violet
<tb> 8. <SEP> - <SEP> monobenzoyl-1.4-diamino- <SEP> crystal powder <SEP> violet <SEP> grass green <SEP> green <SEP> violet
<tb> anthraquinone
<tb>
** WARNING ** End of DESC field may overlap beginning of CLMS **.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT29216T | 1906-07-16 | ||
| DE49485X | 1909-10-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT49485B true AT49485B (en) | 1911-08-25 |
Family
ID=25599274
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT49485D AT49485B (en) | 1906-07-16 | 1910-09-05 | Process for the preparation of vat-coloring arylaminoanthraquinones. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT49485B (en) |
-
1910
- 1910-09-05 AT AT49485D patent/AT49485B/en active
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