DE175396C - - Google Patents
Info
- Publication number
- DE175396C DE175396C DENDAT175396D DE175396DA DE175396C DE 175396 C DE175396 C DE 175396C DE NDAT175396 D DENDAT175396 D DE NDAT175396D DE 175396D A DE175396D A DE 175396DA DE 175396 C DE175396 C DE 175396C
- Authority
- DE
- Germany
- Prior art keywords
- salt
- red
- barite
- insoluble
- hot water
- 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.)
- Active
Links
- 239000000975 dye Substances 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 5
- 125000003277 amino group Chemical group 0.000 claims description 4
- -1 p-dichlorotoluidine Chemical compound 0.000 claims description 4
- RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 3
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methyl-N-phenylamine Natural products CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 claims description 2
- 238000002844 melting Methods 0.000 claims description 2
- 230000008018 melting Effects 0.000 claims description 2
- BHAAPTBBJKJZER-UHFFFAOYSA-N p-anisidine Chemical compound COC1=CC=C(N)C=C1 BHAAPTBBJKJZER-UHFFFAOYSA-N 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical class [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 2
- XQVCBOLNTSUFGD-UHFFFAOYSA-N 3-chloro-4-methoxyaniline Chemical compound COC1=CC=C(N)C=C1Cl XQVCBOLNTSUFGD-UHFFFAOYSA-N 0.000 claims 1
- QSNSCYSYFYORTR-UHFFFAOYSA-N 4-chloroaniline Chemical compound NC1=CC=C(Cl)C=C1 QSNSCYSYFYORTR-UHFFFAOYSA-N 0.000 claims 1
- 235000015250 liver sausages Nutrition 0.000 claims 1
- 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 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 239000000460 chlorine Substances 0.000 description 12
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 6
- 125000001309 chloro group Chemical group Cl* 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 239000004922 lacquer Substances 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 150000001448 anilines Chemical class 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- PPKPKFIWDXDAGC-IHWYPQMZSA-N (z)-1,2-dichloroprop-1-ene Chemical compound C\C(Cl)=C\Cl PPKPKFIWDXDAGC-IHWYPQMZSA-N 0.000 description 1
- FOHHWGVAOVDVLP-UHFFFAOYSA-N 4-chloro-3-nitroaniline Chemical compound NC1=CC=C(Cl)C([N+]([O-])=O)=C1 FOHHWGVAOVDVLP-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001804 chlorine Chemical class 0.000 description 1
- 125000003963 dichloro group Chemical group Cl* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- DADSZOFTIIETSV-UHFFFAOYSA-N n,n-dichloroaniline Chemical compound ClN(Cl)C1=CC=CC=C1 DADSZOFTIIETSV-UHFFFAOYSA-N 0.000 description 1
- RZLBOHUWUYLABB-UHFFFAOYSA-N n-(2,3-dimethylphenyl)nitramide Chemical class CC1=CC=CC(N[N+]([O-])=O)=C1C RZLBOHUWUYLABB-UHFFFAOYSA-N 0.000 description 1
- UUVCWFCUJDNOCH-UHFFFAOYSA-N n-chloro-2,3-dimethylaniline Chemical class CC1=CC=CC(NCl)=C1C UUVCWFCUJDNOCH-UHFFFAOYSA-N 0.000 description 1
- LPEZIAPDJJLVHP-UHFFFAOYSA-N n-chloro-4-methylaniline Chemical compound CC1=CC=C(NCl)C=C1 LPEZIAPDJJLVHP-UHFFFAOYSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/16—Naphthol-sulfonic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE175396C true DE175396C (en:Method) |
Family
ID=440050
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT175396D Active DE175396C (en:Method) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE175396C (en:Method) |
-
0
- DE DENDAT175396D patent/DE175396C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE175396C (en:Method) | ||
| DE1644251A1 (de) | Verfahren zur Herstellung alkoholloeslicher Farbsalze | |
| DE162636C (en:Method) | ||
| DE2949517A1 (de) | Konzentrierte waessrige loesungen von monoazofarbstoffen und deren verwendung zum faerben von papier | |
| DE2622806C3 (de) | Monoazopigment und dessen Verwendung | |
| DE121868C (en:Method) | ||
| DE959393C (de) | Verfahren zur Herstellung von Pigmentfarbstoffen | |
| DE241723C (en:Method) | ||
| DE520239C (de) | Verfahren zur Darstellung von Azofarbstoffen | |
| DE76118C (de) | Verfahren zur Darstellung von primären Disazofarbstoffen mit m-Phenylendiamindisulfosäure | |
| DE237742C (en:Method) | ||
| DE180089C (en:Method) | ||
| DE714864C (de) | Verfahren zur Herstellung von wasserunloeslichen Monoazofarbstoffen | |
| DE472488C (de) | Verfahren zur Darstellung lichtechter gelber Monoazofarbstoffe | |
| DE164990C (en:Method) | ||
| DE543229C (de) | Dauerelektrode fuer elektrische OEfen | |
| DE146655C (en:Method) | ||
| DE275040C (en:Method) | ||
| DE122149C (en:Method) | ||
| DE667860C (de) | Verfahren zur Herstellung von Trisazofarbstoffen | |
| DE723845C (de) | Verfahren zur Herstellung eines wasserloeslichen Monoazofarbstoffs | |
| DE632135C (de) | Verfahren zur Herstellung von Disazofarbstoffen | |
| DE163141C (en:Method) | ||
| DE121867C (en:Method) | ||
| DE101286C (en:Method) |