DE135016C - - Google Patents
Info
- Publication number
- DE135016C DE135016C DENDAT135016D DE135016DA DE135016C DE 135016 C DE135016 C DE 135016C DE NDAT135016 D DENDAT135016 D DE NDAT135016D DE 135016D A DE135016D A DE 135016DA DE 135016 C DE135016 C DE 135016C
- Authority
- DE
- Germany
- Prior art keywords
- toluene
- nitro
- dye
- sulfamidotoluene
- wool
- 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 17
- 150000008049 diazo compounds Chemical class 0.000 claims description 8
- 150000002828 nitro derivatives Chemical class 0.000 claims description 2
- 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
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- OXNIZHLAWKMVMX-UHFFFAOYSA-N Picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 9
- 210000002268 Wool Anatomy 0.000 description 9
- 229940114148 picric acid Drugs 0.000 description 9
- 229950002929 trinitrophenol Drugs 0.000 description 9
- 238000002844 melting Methods 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- VYZAMTAEIAYCRO-UHFFFAOYSA-N chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 5
- 239000000155 melt Substances 0.000 description 5
- 235000011121 sodium hydroxide Nutrition 0.000 description 5
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-Toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Substances ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- PZKPUGIOJKNRQZ-UHFFFAOYSA-N 1-methylcyclohexa-3,5-diene-1,3-diamine Chemical class CC1(N)CC(N)=CC=C1 PZKPUGIOJKNRQZ-UHFFFAOYSA-N 0.000 description 1
- DLURHXYXQYMPLT-UHFFFAOYSA-N 2-nitro-p-toluidine Chemical compound CC1=CC=C(N)C([N+]([O-])=O)=C1 DLURHXYXQYMPLT-UHFFFAOYSA-N 0.000 description 1
- CSKNSYBAZOQPLR-UHFFFAOYSA-N Benzenesulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CC=C1 CSKNSYBAZOQPLR-UHFFFAOYSA-N 0.000 description 1
- QXYMVUZOGFVPGH-UHFFFAOYSA-N Picramic acid Chemical compound NC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O QXYMVUZOGFVPGH-UHFFFAOYSA-N 0.000 description 1
- NVBFHJWHLNUMCV-UHFFFAOYSA-N Sulfamide Chemical compound NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000009963 fulling Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- -1 p-toluenesulfonyl Chemical group 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001376 precipitating Effects 0.000 description 1
- 239000003638 reducing agent Substances 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 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
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE135016C true DE135016C (xx) |
Family
ID=403090
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT135016D Active DE135016C (xx) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE135016C (xx) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE748473C (de) * | 1936-11-19 | 1944-11-03 | Verfahren zur Herstellung von wasserunloeslichen Monoazofarbstoffen | |
| DE1243137B (de) * | 1959-09-16 | 1967-06-29 | Ici Ltd | Verfahren zum Faerben von Textilmaterialien |
| US5446425A (en) * | 1993-06-07 | 1995-08-29 | Atr Optical And Radio Communications Research Laboratories | Floating potential conductor coupled quarter-wavelength coupled line type directional coupler comprising cut portion formed in ground plane conductor |
| EP0887346A2 (en) * | 1997-06-23 | 1998-12-30 | F. Hoffmann-La Roche Ag | Phenyl-and aminophenyl-alkylsulfonamide and urea derivatives, their preparation and their use as alpha1A/1L adrenoceptor agonists |
| EP1398020A1 (en) * | 2002-09-16 | 2004-03-17 | Kao Corporation | Hair dye composition comprising an azo dye containing a dissociative proton, method and use |
| EP1398022A1 (en) * | 2002-09-16 | 2004-03-17 | Kao Corporation | Hair dye composition comprising an azo dye containing a dissociative proton, method and use |
-
0
- DE DENDAT135016D patent/DE135016C/de active Active
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE748473C (de) * | 1936-11-19 | 1944-11-03 | Verfahren zur Herstellung von wasserunloeslichen Monoazofarbstoffen | |
| DE1243137B (de) * | 1959-09-16 | 1967-06-29 | Ici Ltd | Verfahren zum Faerben von Textilmaterialien |
| US5446425A (en) * | 1993-06-07 | 1995-08-29 | Atr Optical And Radio Communications Research Laboratories | Floating potential conductor coupled quarter-wavelength coupled line type directional coupler comprising cut portion formed in ground plane conductor |
| EP0887346A2 (en) * | 1997-06-23 | 1998-12-30 | F. Hoffmann-La Roche Ag | Phenyl-and aminophenyl-alkylsulfonamide and urea derivatives, their preparation and their use as alpha1A/1L adrenoceptor agonists |
| EP0887346A3 (en) * | 1997-06-23 | 1999-05-06 | F. Hoffmann-La Roche Ag | Phenyl-and aminophenyl-alkylsulfonamide and urea derivatives, their preparation and their use as alpha1A/1L adrenoceptor agonists |
| US5952362A (en) * | 1997-06-23 | 1999-09-14 | Syntex (U.S.A) Inc. | 2-imidazoline, 2-oxazoline, 2-thiazoline, and 4-imidazole derivatives of methylphenyl, methoxyphenyl, and aminophenyl alkylsulfonamides and ureas and their use |
| US6057349A (en) * | 1997-06-23 | 2000-05-02 | F. Hoffman La Roche Ag | 2-imidazoline, 2-oxazoline, 2-thiazoline, and 4-imidazole derivatives of methylphenyl, methoxphenyl, and aminophenyl alkylsulfonamides and ureas and their use |
| EP1398020A1 (en) * | 2002-09-16 | 2004-03-17 | Kao Corporation | Hair dye composition comprising an azo dye containing a dissociative proton, method and use |
| EP1398022A1 (en) * | 2002-09-16 | 2004-03-17 | Kao Corporation | Hair dye composition comprising an azo dye containing a dissociative proton, method and use |
| US7056355B2 (en) | 2002-09-16 | 2006-06-06 | Kao Corporation | Hair dye composition and dyeing method |
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