Name | tetradifon |
Synonyms | TEDION TEDONE tetradifon TEDION V-18 TEDION V-18(R) 3,4,6,4'-tetrachlor-diphenylsulfon 2,4,5,4'-Tetrachlorodiphenylsulfone 2,4,5,4'-Tetrachlorodiphenylsulphone 2,4,5,4'-tetrachlorodiphenylsulphone 2,4,5,4'-Tetrachlorodiphenyl sulfone P-CHLOROPHENYL-2,4,5-TRICHLOROPHENYL SULFONE 4-chlorophenyl 2,4,5-trichlorophenyl sulphone 1,2,4-Trichloro-5-[(4-chlorophenyl)sulfonyl]benzene 1,2,4-trichloro-5-((4-chlorophenyl)sulfonyl)-benzen 1,2,4-trichloro-5-((4-chlorophenyl)-sulfonyl)benzene |
CAS | 116-29-0 |
EINECS | 204-134-2 |
InChI | InChI=1/C12H6Cl4O2S/c13-7-1-3-8(4-2-7)19(17,18)12-6-10(15)9(14)5-11(12)16/h1-6H |
Molecular Formula | C12H6Cl4O2S |
Molar Mass | 356.05 |
Density | 1.5630 (estimate) |
Melting Point | 146.5-147.5° |
Boling Point | 484.0±45.0 °C(Predicted) |
Flash Point | 246.5°C |
Water Solubility | 50ug/L(10 ºC) |
Vapor Presure | 4.72E-09mmHg at 25°C |
Appearance | neat |
Merck | 13,9273 |
BRN | 2292528 |
Storage Condition | 0-6°C |
Refractive Index | 1.623 |
Physical and Chemical Properties | Pure white crystals, no smell; Industrial products for yellow or yellow yellow powder. m.p.145 -146 °c (industrial 120-140 °c), vapor pressure of 3.199 x 10-8Pa (20 °c). Slightly soluble in ethanol, acetone, benzene, xylene, chloroform and other organic solvents; Insoluble in water. Chemical stability, the general acid, alkali solution, high temperature and UV light is not easy to decompose, non-corrosive. |
Use | It has a good effect of killing acaricidal eggs and juvenile mites, and the residual effect period is up to 40 ~ 50d, which can be used to control the initial hatching mites, egg peak period or less adult mites of cotton, citrus, Apple and other plants. The use of content. 05%, can inhibit the female mite oviposition and infertility. |
Risk Codes | R22 - Harmful if swallowed R50/53 - 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 | UN3077 9/PG 3 |
WGK Germany | 3 |
RTECS | WR5850000 |
Toxicity | LD50 orally in rats: 556 mg/kg (Ben-dyke) |
Reference Show more | 1. Peng Zhenfei, Huang Hui, Li Yongning, et al. Determination of dicofol in tea by ultra performance liquid chromatography [J]. Anhui Agricultural Sciences, 2020, 048(003):200-202 |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
toxicity | acute oral LD50>5000 mg/kg in rats. Feeding rats with a dose of 500mg/kg for 2 months, no harmful effects were found, and feeding rats with a dose of 1000mg/kg for 60 days, no abnormal phenomena of their offspring were found. |
use | has a good effect of killing mites and young mites, with a residual period of 40 ~ 50d, and can be used to prevent cotton, citrus, apple and other plants from hatching mites, egg peak or less mites. Use content. 05%, can inhibit female mite oviposition and infertility. this product is a contact acaricide, which is used to control mites of fruit trees, cotton and vegetables. When the concentration is 0.05%, it can inhibit female mites from laying eggs and making them sterile. used to control pests such as hawthorn spider mites, apple whole melon mites, citrus whole melon mites and spider mites trichloroacilone is a contact acaricide, used to control fruit trees, cotton, and vegetables Mites. When the concentration is 0.05%, it can inhibit female mites from laying eggs and making them sterile. |
Production method | The intermediate trichlorobenzene sulfonyl chloride is prepared by chlorosulfonation of trichlorobenzene, which is then condensed with chlorobenzene in the presence of aluminum trichloride to obtain trichloroacilone. Raw material consumption quota: trichlorobenzene 750kg/t, chlorosulfonic acid 1570kg/t, trichlorobenzenesulfonyl chloride 990kg/t, chlorobenzene 440kg/t, aluminum trichloride 500kg/t. chlorosulfonation trichlorobenzene is added dropwise to chlorosulfonic acid, the chlorosulfonic acid is excessive, the reaction temperature is 80~90 ℃, and the chlorosulfonation time is 3h. The gas discharged from the reaction is absorbed with water. The generated trichlorobenzenesulfonyl chloride is cooled and precipitated, washed with water (if necessary, a small amount of nitric acid is added to oxidize the low-sulfur compound into trichlorobenzenesulfonyl chloride), and finally it is dehydrated and dried for condensation. Condensation of trichlorobenzenesulfonyl chloride and chlorobenzene to produce trichloroacilone. The reaction is an electrophilic secondary reaction, using AlCl3 or FeCl3 as catalyst, chlorobenzene is added dropwise, the reaction temperature is 145~155 ℃, and the reaction time is 1.5~3h. The condensation product is poured into 90 ℃ hot water, stirred to precipitate trichloroacilone, washed and dried to obtain raw powder. |
category | pesticide |
toxicity classification | poisoning |
acute toxicity | oral-rat LD50: 566 mg/kg; Oral-dog LD50: 2000 mg/kg |
flammability hazard characteristics | Combustion produces toxic sulfur oxides and chloride gases |
storage and transportation characteristics | warehouse ventilation and low temperature drying; Store separately from oxidant (ammonium nitrate) and food additives |
fire extinguishing agent | water, foam, sand. |
toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |