DE216223C - - Google Patents
Info
- Publication number
 - DE216223C DE216223C DENDAT216223D DE216223DA DE216223C DE 216223 C DE216223 C DE 216223C DE NDAT216223 D DENDAT216223 D DE NDAT216223D DE 216223D A DE216223D A DE 216223DA DE 216223 C DE216223 C DE 216223C
 - Authority
 - DE
 - Germany
 - Prior art keywords
 - acid
 - dye
 - parts
 - diazo compound
 - solution
 - 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.)
 - Expired
 
Links
- 239000002253 acid Substances 0.000 claims description 11
 - 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 10
 - 150000008049 diazo compounds Chemical class 0.000 claims description 7
 - QYFYIOWLBSPSDM-UHFFFAOYSA-N 6-aminonaphthalen-1-ol Chemical compound OC1=CC=CC2=CC(N)=CC=C21 QYFYIOWLBSPSDM-UHFFFAOYSA-N 0.000 claims description 3
 - 238000000034 method Methods 0.000 claims description 3
 - 239000003929 acidic solution Substances 0.000 claims description 2
 - 239000012670 alkaline solution Substances 0.000 claims description 2
 - 239000013067 intermediate product Substances 0.000 claims description 2
 - 239000000975 dye Substances 0.000 description 20
 - 239000000243 solution Substances 0.000 description 9
 - QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
 - HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
 - OUFRIWNNMFWZTM-UHFFFAOYSA-M sodium arsanilate Chemical group [Na+].NC1=CC=C([As](O)([O-])=O)C=C1 OUFRIWNNMFWZTM-UHFFFAOYSA-M 0.000 description 6
 - NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 5
 - XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
 - QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
 - 229910052785 arsenic Inorganic materials 0.000 description 3
 - RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 3
 - 201000010099 disease Diseases 0.000 description 3
 - 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
 - RBDJQFKUZPMOFH-UHFFFAOYSA-I pentasodium;3-amino-4-[[4-[4-[(2-amino-3,6-disulfonatonaphthalen-1-yl)diazenyl]-3-sulfonatophenyl]phenyl]diazenyl]naphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].C12=CC=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(N)=C1N=NC1=CC=C(C=2C=C(C(N=NC=3C4=CC=C(C=C4C=C(C=3N)S([O-])(=O)=O)S([O-])(=O)=O)=CC=2)S([O-])(=O)=O)C=C1 RBDJQFKUZPMOFH-UHFFFAOYSA-I 0.000 description 3
 - 238000003756 stirring Methods 0.000 description 3
 - RNXVXXXZBIXZMS-UHFFFAOYSA-N (4-aminophenyl)arsinic acid Chemical compound NC1=CC=C([AsH](O)=O)C=C1 RNXVXXXZBIXZMS-UHFFFAOYSA-N 0.000 description 2
 - VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
 - 241000699670 Mus sp. Species 0.000 description 2
 - FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
 - YKQNYRADBBHWOK-UHFFFAOYSA-N phenylarsonamidic acid Chemical compound N[As](O)(=O)C1=CC=CC=C1 YKQNYRADBBHWOK-UHFFFAOYSA-N 0.000 description 2
 - 239000000725 suspension Substances 0.000 description 2
 - 241000947840 Alteromonadales Species 0.000 description 1
 - 229910000906 Bronze Inorganic materials 0.000 description 1
 - LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
 - IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
 - CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
 - 238000009825 accumulation Methods 0.000 description 1
 - 230000002378 acidificating effect Effects 0.000 description 1
 - VJWWIRSVNSXUAC-UHFFFAOYSA-N arsinic acid Chemical class O[AsH2]=O VJWWIRSVNSXUAC-UHFFFAOYSA-N 0.000 description 1
 - 239000000987 azo dye Substances 0.000 description 1
 - 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
 - 230000015572 biosynthetic process Effects 0.000 description 1
 - 239000010974 bronze Substances 0.000 description 1
 - 238000006243 chemical reaction Methods 0.000 description 1
 - 239000007795 chemical reaction product Substances 0.000 description 1
 - KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 1
 - 230000008878 coupling Effects 0.000 description 1
 - 238000010168 coupling process Methods 0.000 description 1
 - 238000005859 coupling reaction Methods 0.000 description 1
 - UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 description 1
 - 238000004090 dissolution Methods 0.000 description 1
 - 239000003814 drug Substances 0.000 description 1
 - 230000000694 effects Effects 0.000 description 1
 - 239000000706 filtrate Substances 0.000 description 1
 - 238000001914 filtration Methods 0.000 description 1
 - 230000035876 healing Effects 0.000 description 1
 - 230000002045 lasting effect Effects 0.000 description 1
 - 231100001231 less toxic Toxicity 0.000 description 1
 - 230000008560 physiological behavior Effects 0.000 description 1
 - 239000002244 precipitate Substances 0.000 description 1
 - 238000001556 precipitation Methods 0.000 description 1
 - 239000000047 product Substances 0.000 description 1
 - 159000000000 sodium salts Chemical class 0.000 description 1
 - 239000000126 substance Substances 0.000 description 1
 - 231100000419 toxicity Toxicity 0.000 description 1
 - 230000001988 toxicity Effects 0.000 description 1
 - 230000001742 trypanosomicidal effect Effects 0.000 description 1
 
Classifications
- 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
 - C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
 - C07F9/66—Arsenic compounds
 - C07F9/70—Organo-arsenic compounds
 - C07F9/74—Aromatic compounds
 
 
Landscapes
- Chemical & Material Sciences (AREA)
 - Organic Chemistry (AREA)
 - Coloring (AREA)
 
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| DE190907905X | 1908-04-14 | 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| DE216223C true DE216223C (enEXAMPLES) | 1900-01-01 | 
Family
ID=32405255
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| DENDAT216223D Expired DE216223C (enEXAMPLES) | 1908-04-14 | 
Country Status (2)
| Country | Link | 
|---|---|
| DE (1) | DE216223C (enEXAMPLES) | 
| GB (1) | GB190907905A (enEXAMPLES) | 
- 
        0
        
- DE DENDAT216223D patent/DE216223C/de not_active Expired
 
 - 
        1909
        
- 1909-04-02 GB GB190907905D patent/GB190907905A/en not_active Expired
 
 
Also Published As
| Publication number | Publication date | 
|---|---|
| GB190907905A (en) | 1909-05-27 | 
Similar Documents
| Publication | Publication Date | Title | 
|---|---|---|
| DE1132540B (de) | Verfahren zur Herstellung von Loesungen von Kupplungskomponenten der Eisfarbenreihe | |
| DE216223C (enEXAMPLES) | ||
| DE148875C (enEXAMPLES) | ||
| DE2504068C2 (de) | Triazo-farbstoff und Verfahren zu seiner Herstellung | |
| DE725224C (de) | Verfahren zur Herstellung von Trisazofarbstoffen | |
| DE971896C (de) | Verfahren zur Herstellung kobalthaltiger Azofarbstoffe | |
| DE633786C (de) | Verfahren zur Herstellung von Komplexverbindungen des 1, 3-Dimethylxanthins | |
| DE193740C (enEXAMPLES) | ||
| DE513209C (de) | Verfahren zur Darstellung von Diazoaminoverbindungen | |
| DE531222C (de) | Verfahren zur Darstellung von Wismutdithioglykolsaeure und ihren Salzen | |
| DE254187C (enEXAMPLES) | ||
| DE254421C (enEXAMPLES) | ||
| DE742325C (de) | Verfahren zur Herstellung von Trisazofarbstoffen | |
| DE949104C (de) | Verfahren zur Herstellung fester, haltbarer Diazonium-Verbindungen | |
| CH616447A5 (enEXAMPLES) | ||
| DE270258C (enEXAMPLES) | ||
| DE79564C (enEXAMPLES) | ||
| DE459362C (de) | Verfahren zur Darstellung von wasserloeslichen Kondensationsprodukten der Aminoarylarsinsaeuren | |
| AT135691B (de) | Verfahren zur Darstellung von 1-Oxy-2-methoxy-6-aminobenzolarsinsäuren und deren Reduktions-produkten. | |
| DE256858C (enEXAMPLES) | ||
| AT114530B (de) | Verfahren zur Darstellung neuer unsymmetrischer Arsenoverbindungen. | |
| DE620908C (de) | Verfahren zur Herstellung von heteronuclearen Halogenaminoanthrachinonsulfonsaeuren | |
| DE415095C (de) | Verfahren zur Herstellung einer in Wasser leicht loeslichen Wismutkomplexverbindung der Chinolinreihe | |
| DE704549C (de) | Verfahren zur Herstellung von Pplyjodoxyphenylphenylessigsaeuren | |
| DE237787C (enEXAMPLES) |