Name | naphthol as-D |
Synonyms | C.I. 37520 Naphtol AS-D naphthol as-D AcnaNaphtholE Acna Naphthol E C.I. Developer 21 Acco Naf-Sol AS-D Acco Naphthol AS-D Amanil Naphthol AS-D Azoic coupling component 18 C.I. Azoic Coupling Component 18 2-Naphtho-o-toluidide, 3-hydroxy- 2-Hydroxy-3-Naphthoyl-O-Toluidine C.I. Azoic Coupling Component 110 naphthol as-D type iii repurified 3-hydroxy-2-methyl-2-naphthanilide 1-(2',3'-Hydroxynaphthoylamino)-2-methylbenzene 3-hydroxy-n-(2-methylphenyl)-2-naphthalenecarboxamid 3-hydroxy-N-(2-methylphenyl)naphthalene-2-carboxamide |
CAS | 135-61-5 |
EINECS | 205-205-0 |
InChI | InChI=1/C18H15NO2/c1-12-6-2-5-9-16(12)19-18(21)15-10-13-7-3-4-8-14(13)11-17(15)20/h2-11,20H,1H3,(H,19,21) |
Molecular Formula | C18H15NO2 |
Molar Mass | 277.32 |
Density | 1.277±0.06 g/cm3(Predicted) |
Melting Point | 196-198°C |
Boling Point | 399.7±35.0 °C(Predicted) |
Flash Point | 195.5°C |
Vapor Presure | 5.83E-07mmHg at 25°C |
Appearance | Pale yellow powder |
Color | White to Gray to Brown |
pKa | 8.73±0.40(Predicted) |
Storage Condition | Room Temprature |
Refractive Index | 1.715 |
MDL | MFCD00021634 |
Physical and Chemical Properties | Characteristic beige powder. melting point 195~196 ℃ solubility in solvent naphtha. Insoluble in water and soda ash solution. |
Use | Mainly used for the production of insoluble azo dyes and used for cotton fiber, viscose fiber and some synthetic fiber dyeing and printing |
Hazard Symbols | N - Dangerous for the environment |
Risk Codes | 50/53 - Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. |
Safety Description | S60 - This material and its container must be disposed of as hazardous waste. S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. |
UN IDs | UN 3077 9/PG 3 |
WGK Germany | 2 |
Hazard Class | 9 |
Packing Group | III |
color index | 37520 |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
use | mainly used for producing insoluble azo dyes and for dyeing and printing of cotton fibers, viscose fibers and some synthetic fibers tryptopol AS-D is the main red primer for dyeing cotton fibers. The performance is similar to that of tryptopol AS, so it can be mixed to adjust the color light. Dye date red with red base B and rose red with red base RL. It is also used for dyeing vinylon, viscose fiber, silk and diacetate fiber. Chromophenol is AS-D used as a base agent for cotton printing. It can be combined with different color bases to obtain orange, red, purple and blue colors. Low affinity to cotton and moderate coupling ability. It is also used to make fast pigments and lake pigments. It is mainly used as a primer for dyeing and printing of cotton fabrics, and can be used as an intermediate for fast pigments and organic pigments. |
production method | 2,3-acid is salted and dehydrated with chlorobenzene and sodium carbonate, then condensed with o-toluidine in the presence of phosphorus trichloride, neutralized with sodium carbonate, evaporated to chlorobenzene, filtered and dried to obtain the finished product. Raw material consumption (kg/t)2,3-acid 750 o-toluidine 430 chlorobenzene 200 sodium carbonate 450 450 phosphorus trichloride 280 using 2,3-acid and o-toluidine as raw materials, the 2,3-acid is first prepared into sodium salt in chlorobenzene medium, then condensed with o-toluidine in the presence of PCl3, neutralized, distilled, filtered and dried to obtain the finished product.. Add 4000-4500L of chlorobenzene, 2,3-acid 630kg (100%) and 280kg of sodium carbonate to the salt-forming pot, heat to 45 ℃, continue to raise the temperature to 134-135 ℃ after carbon dioxide escapes, continuously dehydrate, stop heating when the chlorobenzene to be distilled does not contain water, and the volume of feed liquid is about 2800-3000L. The above salt-forming reaction is hydraulically put into a condensation kettle, cooled to 90 ℃, o-toluidine 430kg (98%) is added, cooling to 65-70 ℃ is continued, phosphorus trichloride-chlorobenzene mixed solution (230kg PCl3 is prepared into 55%-60% mixed solution with anhydrous chlorobenzene) is added within 2 hours, and the temperature is kept at 119-120 ℃ for 2 hours after adding. Add 1000L of water and 330L of 30% sodium hydroxide solution in the distillation kettle, then press the above condensate, stir for 15min, and determine the pH value at 8-8.5. Then direct steam distillation is used until the distillate is clear and free of chlorobenzene. Add hot water above 90 ℃ until the volume of the material reaches about 5000L, filter, wash the filter cake with hot water above 90 ℃ until the filtrate is clarified, drain the water, and dry the finished product to about 885kg. In the condensation reaction, the solvent must be anhydrous (that is, the moisture content should be below 1%), and the hydrogen chloride must be fully eliminated, otherwise the product yield will be seriously affected. |