AT29526B - Process for the preparation of halogen derivatives of anthracene dyes. - Google Patents
Process for the preparation of halogen derivatives of anthracene dyes.Info
- Publication number
- AT29526B AT29526B AT29526DA AT29526B AT 29526 B AT29526 B AT 29526B AT 29526D A AT29526D A AT 29526DA AT 29526 B AT29526 B AT 29526B
- Authority
- AT
- Austria
- Prior art keywords
- sep
- blue
- violet
- preparation
- halogen derivatives
- Prior art date
Links
- -1 halogen derivatives of anthracene Chemical class 0.000 title description 3
- 239000000975 dye Substances 0.000 title description 2
- 229910052736 halogen Inorganic materials 0.000 title 1
- 244000172533 Viola sororia Species 0.000 description 9
- 235000005811 Viola adunca Nutrition 0.000 description 4
- 240000009038 Viola odorata Species 0.000 description 4
- 235000013487 Viola odorata Nutrition 0.000 description 4
- 235000002254 Viola papilionacea Nutrition 0.000 description 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 1
- AXDJCCTWPBKUKL-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydron;chloride Chemical compound Cl.C1=CC(=N)C(C)=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 AXDJCCTWPBKUKL-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- GRWZHXKQBITJKP-UHFFFAOYSA-N dithionous acid Chemical compound OS(=O)S(O)=O GRWZHXKQBITJKP-UHFFFAOYSA-N 0.000 description 1
- ORFSSYGWXNGVFB-UHFFFAOYSA-N sodium 4-amino-6-[[4-[4-[(8-amino-1-hydroxy-5,7-disulfonaphthalen-2-yl)diazenyl]-3-methoxyphenyl]-2-methoxyphenyl]diazenyl]-5-hydroxynaphthalene-1,3-disulfonic acid Chemical compound COC1=C(C=CC(=C1)C2=CC(=C(C=C2)N=NC3=C(C4=C(C=C3)C(=CC(=C4N)S(=O)(=O)O)S(=O)(=O)O)O)OC)N=NC5=C(C6=C(C=C5)C(=CC(=C6N)S(=O)(=O)O)S(=O)(=O)O)O.[Na+] ORFSSYGWXNGVFB-UHFFFAOYSA-N 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
Landscapes
- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
Description
<Desc/Clms Page number 1>
EMI1.1
EMI1.2
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EMI2.2
<tb>
<tb>
Farbe <SEP> der
<tb> Küpenfarbe
<tb> Konzentrierte <SEP> alkalischen
<tb> Warmes <SEP> Nitrobenzol <SEP> Warmes <SEP> Anilin <SEP> auf
<tb> Rohfarbstoffe <SEP> H2SO4 <SEP> HydrosulfitBaumwolle
<tb> küpe
<tb> schwer <SEP> löslich
<tb> Cyananthren <SEP> trübe <SEP> grün <SEP> grünolive <SEP> braunrote <SEP> blaugrün <SEP> violettblau <SEP> blauviolett
<tb> Fluoreszene
<tb> schwer <SEP> löslich
<tb> Brom-Cyananthren
<tb> dto.
<SEP> grünlich <SEP> brauurote <SEP> blaugrün <SEP> blau <SEP> violettblau
<tb> nach <SEP> Beispiel <SEP> I
<tb> Fluoreszene
<tb> schwer <SEP> löslich
<tb> Chlor-Cyananthren
<tb> grün <SEP> grünlich <SEP> braunrote <SEP> grünblau <SEP> blau <SEP> blauviolett
<tb> nach <SEP> Beispiel <SEP> II
<tb> Fluoreszene
<tb> schwer <SEP> löslich
<tb> Chlor-Cyananthren <SEP> lebhaft
<tb> blaugrün <SEP> blau <SEP> braunrote <SEP> blau <SEP> grünlich <SEP> blau
<tb> nach <SEP> Beispiel <SEP> III <SEP> violett
<tb> Fluoreszenz
<tb> rot <SEP> violett <SEP> braun- <SEP> gut <SEP> löslich
<tb> Violauthren <SEP> trüb <SEP> violett <SEP> fuchsinrot <SEP> vioilett
<tb> rote <SEP> Fluoreszenz <SEP> reinblau
<tb> violettblau <SEP> starke
<tb> Brom-Violanthren <SEP> sehr <SEP> blaues
<tb> dto.
<SEP> braunrote <SEP> grünblau <SEP> violettrot
<tb> nach <SEP> Beispiel <SEP> I <SEP> violettblau
<tb> Fluoreszenz
<tb> Chlor-Violanthren <SEP> violett <SEP> braunrote <SEP> lebhaftes
<tb> dto. <SEP> blauvioilett <SEP> blauviolett
<tb> nach <SEP> Beispiel <SEP> II <SEP> Fluoreszenz <SEP> rotviolett
<tb> Chlor-Violanthren <SEP> violett <SEP> braunrote <SEP> sehr <SEP> blaues
<tb> dto. <SEP> violettblau <SEP> grünblau
<tb> nach <SEP> Beispiel <SEP> III <SEP> Fluoreszenz <SEP> violettblau
<tb>
<Desc / Clms Page number 1>
EMI1.1
EMI1.2
<Desc / Clms Page number 2>
EMI2.1
EMI2.2
<tb>
<tb>
Color <SEP> the
<tb> vat color
<tb> Concentrated <SEP> alkaline
<tb> Warm <SEP> nitrobenzene <SEP> warm <SEP> aniline <SEP>
<tb> raw dyes <SEP> H2SO4 <SEP> hydrosulphite cotton
<tb> vat
<tb> poorly <SEP> soluble
<tb> Cyananthrene <SEP> cloudy <SEP> green <SEP> green-olive <SEP> brown-red <SEP> blue-green <SEP> violet-blue <SEP> blue-violet
<tb> fluorescent scene
<tb> poorly <SEP> soluble
<tb> bromo-cyananthrene
<tb> dto.
<SEP> greenish <SEP> brownish red <SEP> blue-green <SEP> blue <SEP> violet-blue
<tb> according to <SEP> example <SEP> I
<tb> fluorescent scene
<tb> poorly <SEP> soluble
<tb> chlorine cyananthrene
<tb> green <SEP> greenish <SEP> brown-red <SEP> green-blue <SEP> blue <SEP> blue-violet
<tb> according to <SEP> example <SEP> II
<tb> fluorescent scene
<tb> poorly <SEP> soluble
<tb> Chlor-Cyananthrene <SEP> lively
<tb> blue-green <SEP> blue <SEP> brown-red <SEP> blue <SEP> greenish <SEP> blue
<tb> according to <SEP> example <SEP> III <SEP> violet
<tb> fluorescence
<tb> red <SEP> violet <SEP> brown- <SEP> well <SEP> soluble
<tb> Violauthren <SEP> cloudy <SEP> violet <SEP> fuchsin red <SEP> violet
<tb> red <SEP> fluorescence <SEP> pure blue
<tb> violet blue <SEP> strong
<tb> Brom-Violanthren <SEP> very <SEP> blue
<tb> dto.
<SEP> brown-red <SEP> green-blue <SEP> violet-red
<tb> according to <SEP> example <SEP> I <SEP> violet blue
<tb> fluorescence
<tb> Chlor-Violanthren <SEP> violet <SEP> brown-red <SEP> lively
<tb> dto. <SEP> blue-violet <SEP> blue-violet
<tb> according to <SEP> example <SEP> II <SEP> fluorescence <SEP> red-violet
<tb> Chlor-Violanthren <SEP> violet <SEP> brown-red <SEP> very <SEP> blue
<tb> same as <SEP> violet-blue <SEP> green-blue
<tb> according to <SEP> example <SEP> III <SEP> fluorescence <SEP> violet blue
<tb>
Claims (1)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT29526D AT29526B (en) | 1904-12-31 | 1905-11-25 | Process for the preparation of halogen derivatives of anthracene dyes. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT27319T | 1904-12-31 | ||
| AT29526D AT29526B (en) | 1904-12-31 | 1905-11-25 | Process for the preparation of halogen derivatives of anthracene dyes. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT29526B true AT29526B (en) | 1907-08-10 |
Family
ID=25598993
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT29526D AT29526B (en) | 1904-12-31 | 1905-11-25 | Process for the preparation of halogen derivatives of anthracene dyes. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT29526B (en) |
-
1905
- 1905-11-25 AT AT29526D patent/AT29526B/en active
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