Molecular Formula | C8H4Cl6 |
Molar Mass | 312.84 |
Density | 1.6957 (rough estimate) |
Melting Point | 106-110 °C |
Boling Point | 312 °C |
Appearance | Morphological Crystalline Powder and Chunks, color Light yellow |
Storage Condition | Room Temprature |
Refractive Index | 1.5840 (estimate) |
MDL | MFCD00000791 |
Physical and Chemical Properties | Chemical properties White needle crystal or crystalline powder, made of special odor, tasteless. Melting point 108-110 ℃. Insoluble in water, easily soluble in ethanol, xylene, petroleum ether and vegetable oil. When exposed to light and alkali, acid will be formed. |
Use | Widely used in pharmaceutical, pesticide, paint, dye production |
Hazard Symbols | C - Corrosive![]() |
Risk Codes | 34 - Causes burns |
Safety Description | S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
RTECS | ZE4655000 |
HS Code | 29036990 |
Raw Materials | Xylene Benzoyl peroxide Triethanolamine Activated carbon,decolor m-Xylene P-XYLENE |
Downstream Products | 1,4-Bis(trifluoromethyl)-benzene |
use
1. As an anti-schistosomiasis drug, it is effective for liver fluke disease, amoebic disease, malaria and intestinal protozoa in animals.
2. Anti-schistosomiasis drugs. It has certain curative effect on liver fluke disease, amoebic disease, malaria and intestinal nematode. However, adverse reactions to the nervous system are more common, and the delayed reaction lasts for a long time.
production method
1. using mixed xylene as raw material, sulfonate with 98% sulfuric acid first to make m-xylene generate m-xylene sulfonate. The oil layer containing o-and p-xylene is separated from the sulfonated reactant, washed and dried, and distilled o-and p-xylene under reduced pressure. The by-product m-xylene can be obtained by hydrolysis of m-xylene sulfonate. Chlorination of o-and p-xylene yields 1, 4-bis (trichloromethyl) benzene: put o-and p-xylene in the reaction pot, and then add benzoyl peroxide and triethanolamine. After heating to 70 ℃, chlorine gas is introduced under light irradiation, reacted at 70-80 ℃ for 6 hours, and then heated to 100-120 ℃ to continue the reaction until the relative density of the reaction liquid phase reaches 1.560-1.580(65 ℃), which is the end point of the reaction. Chlorine is stopped and residual chlorine is removed under reduced pressure. Cool down to 5 ℃, filter, wash the crude, recrystallize, and decolorize the finished product with activated carbon.
2. It is obtained by chlorination with o-or p-xylene as raw material.
add benzoyl peroxide and triethanolamine to o-or p-xylene, and react with chlorine at 70-80 ℃ for 6h. Then the temperature is raised to 100-120 ℃, and the chlorine gas reaction is continued until the relative density of the feed liquid reaches 1.560-1.580(65 ℃). After the reaction is over, the residual chlorine gas is removed under reduced pressure, cooled to 5 ℃, filtered, washed, decolorized, and recrystallized to obtain the finished product.
Merck | 1303 |
EPA chemical information | p-Di(trichloromethyl)benzene (68-36-0) |
toxic substance data | 68-36-0(Hazardous Substances Data) |