Name | 1,4,5,6,7,7-hexachlorobicyclo[2.2.1]hept-5-ene-2,3-dimethanol |
Synonyms | endodiol thiodandiol chlorendicdiol endosulfandiol 1,4,5,6,7,7-hexachloro-5-norbornene-3-dimethanol 1,4,5,6,7,7-hexachloro-bicyclo(2.2.1)hept-5-ene-3-dimethanol 1,4,5,6,7,7-hexachloro-bicyclo[2.2.1]hept-5-ene-3-dimethanol 1,4,5,6,7,7-hexachlorobicyclo(2.2.1)hept-5-ene-2,3-dimethanol 1,4,5,6,7,7-hexachlorobicyclo[2.2.1]hept-5-ene-2,3-dimethanol |
CAS | 2157-19-9 |
EINECS | 218-467-6 |
InChI | InChI=1/C9H8Cl6O2/c10-5-6(11)8(13)4(2-17)3(1-16)7(5,12)9(8,14)15/h3-4,16-17H,1-2H2 |
Molecular Formula | C9H8Cl6O2 |
Molar Mass | 360.88 |
Density | 1.5459 (estimate) |
Melting Point | 207-208℃ |
Boling Point | 411.8±40.0 °C(Predicted) |
Flash Point | 100°C |
Vapor Presure | 1.68E-08mmHg at 25°C |
Appearance | neat |
BRN | 2057348 |
pKa | 14.62±0.10(Predicted) |
Storage Condition | Room Temprature |
Refractive Index | 1.63 |
Physical and Chemical Properties | Endosulfan alcohol is solid. |
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 |
RTECS | DT5300000 |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
use | endosulfan is an intermediate of the organochlorine insecticide endosulfan. |
production method | there are two methods for the synthesis of endosulfan alcohol: direct method and indirect method. in our country, direct method is mostly used, which is prepared by the reaction of hexachlorocyclopentadiene and butene diol. Put hexachlorocyclopentadiene and solvent into the reaction kettle, stir and heat to the reaction temperature, add butylene glycol dropwise, after the dropwise addition, continue to stir for 10h at the reaction temperature, precipitate endosulfan crystals after cooling, and obtain endosulfan after filtration and solvent washing. |