Name | 2,4,5-Trichlorobenzenesulphonyl chloride |
Synonyms | AKOS 213-16 2,4,5-trichloro-benzenesulfonylchlorid 2,4,5-Trichlorobenzenesulfonyl chloride 2,4,5-TRICHLOROBENZENESULFONYL CHLORIDE 2,4,5-TRICHLOROBENZENESULPHONYL CHLORIDE 2,4,5-Trichlorobenzenesulphonyl chloride 2,4,5-THRICHLOROBENZENESULFONYL CHLORIDE 2,4,5-TRICHLOROBENZENE-1-SULFONYL CHLORIDE |
CAS | 15945-07-0 |
EINECS | 240-079-0 |
InChI | InChI=1/C6H2Cl4O2S/c7-3-1-5(9)6(2-4(3)8)13(10,11)12/h1-2H |
Molecular Formula | C6H2Cl4O2S |
Molar Mass | 279.96 |
Density | 1.728±0.06 g/cm3(Predicted) |
Melting Point | 65-69 °C |
Boling Point | 138 °C(Press: 0.5 Torr) |
Flash Point | 162.4°C |
Vapor Presure | 0.000127mmHg at 25°C |
BRN | 1112595 |
Storage Condition | Inert atmosphere,2-8°C |
Sensitive | Moisture Sensitive |
Refractive Index | 1.593 |
MDL | MFCD00007428 |
Hazard Symbols | C - Corrosive |
Risk Codes | R34 - Causes burns R14 - Reacts violently with water |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S27 - Take off immediately all contaminated clothing. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S8 - Keep container dry. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
UN IDs | 3261 |
WGK Germany | 3 |
TSCA | T |
HS Code | 29049095 |
Hazard Note | Corrosive/Moisture Sensitive |
Hazard Class | 8 |
Packing Group | II |
use | 2,4, 5-trichlorobenzenesulfonyl chloride is abbreviated as sulfonyl chloride, which is an important intermediate for the synthesis of acaricide trichlorosulfone. |
production method | 2,4, 5-trichlorobenzenesulfonyl chloride is made from trichlorobenzene. The metered chlorosulfonic acid is added to the dried chlorosulfonation kettle, stirred at 30~50 ℃, and the metered trichlorobenzene is added dropwise. After addition, the temperature is raised to 80~85 ℃ for 3h. After the reaction is completed, the temperature is reduced to about 40 ℃, and the reaction solution is slowly added dropwise into a water separation kettle with a certain amount of cold water in advance to precipitate sulfonyl chloride at 30~40 ℃. After filtration, washing and drying, the intermediate sulfonyl chloride is obtained with the content ≥ 97% and the yield ≥ 80% (calculated as 1,2, 4-trichlorobenzene). 2,4, 5-trichlorobenzenesulfonyl chloride industrial products are white porous crystals, insoluble in water, soluble in alcohol, benzene, chlorobenzene and other solvents. |
EPA chemical information | information provided by: ofmpub.epa.gov (external link) |