| Molecular Formula | C10H8Cl2N2O4S |
| Molar Mass | 323.15 |
| Density | 1.5186 (rough estimate) |
| Melting Point | 346°C (dec.)(lit.) |
| Appearance | powder to crystal |
| Color | White to Orange to Green |
| pKa | -1.41±0.50(Predicted) |
| Storage Condition | Room Temprature |
| Refractive Index | 1.6000 (estimate) |
| MDL | MFCD00035706 |
| Physical and Chemical Properties | Character white or yellow crystalline powder. soluble in water and ethanol, soluble in alkali, slightly soluble in ether. |
| Use | For the synthesis of C.I. Acid yellow 17, C.I. Acid orange 40, C.I. Reactive yellow 1 and other reactive dyes |
| Hazard Symbols | Xi - Irritant![]() |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
| WGK Germany | 3 |
| RTECS | DB6040000 |
white or yellow crystalline powder, soluble in water and ethanol, soluble in alkali, slightly soluble in ether.
2, 5-chloroaniline was sulfonated and then diazotized with sodium nitrite. The diazonium salt is reduced by sodium sulfite and sodium bisulfite to give 2, 5-chloro-4-sulfonylphenylhydrazine sulfonate sodium salt, which is acidified by sulfuric acid to form sulfate, then condensed with ethyl acetoacetate, and then neutralized by soda ash to remove ethyl ester, re-acidification to obtain finished product.
dye intermediates, mainly used in the manufacture of acid yellow 2G and active yellow M-5G,K-6G,X-6G and so on.
| EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
| Use | for the synthesis of C.I. Acid yellow 17, C.I. Acid orange 40, C.I. Reactive yellow 1 and other reactive dyes |
| production method | 2, 5-dichloroaniline was sulfonated and then diazotized with sodium nitrite. The diazonium salt is reduced by sodium sulfite and sodium bisulfite to obtain sodium 2, 5-dichloro-4-sulfonylphenylhydrazine sulfonate, which is acidified by sulfuric acid to form sulfate, then condensed with ethyl acetoacetate, and then neutralized by soda ash to remove ethyl ester, re-acidification to obtain finished product. |