| Identification | Back Directory | [Name]
EGT | [CAS]
2514-53-6 | [Synonyms]
EGT
GLYTAC(R)
TCA-ethadyl
ethylenglykoltrichloracetat
ETHYLENE BISTRICHLOROACETATE
trichloro-aceticaciethyleneester(2:1)
ETHYLENE GLYCOL BIS[TRICHLOROACETATE]
Bis(trichloroacetic acid)ethylene ester
2-(2,2,2-trichloroacetyl)oxyethyl 2,2,2-trichloroacetate
2-(2,2,2-trichloroethanoyloxy)ethyl 2,2,2-trichloroethanoate
2,2,2-trichloroacetic acid 2-(2,2,2-trichloroacetyl)oxyethyl ester | [EINECS(EC#)]
219-732-9 | [Molecular Formula]
C6H4Cl6O4 | [MDL Number]
MFCD00128020 | [MOL File]
2514-53-6.mol | [Molecular Weight]
352.81 |
| Hazard Information | Back Directory | [Definition]
ChEBI: TCA-ethadyl is a diester. It is functionally related to a trichloroacetic acid and an ethylene glycol. | [Production Methods]
TCA-ethadyl was produced by first generating technical trichloroacetic acid through the standard chlorination-oxidation route from acetic acid or acetaldehyde, then converting it into an ester with ethylene glycol derivatives under controlled acidic conditions. This esterification step yielded the di-(2-hydroxyethyl) trichloroacetate material historically referred to as TCA-ethadyl, which offered improved handling and reduced volatility compared with the free acid. After reaction completion, the product mixture was purified by phase separation and controlled distillation or crystallisation to remove unreacted alcohols and by products. | [Mechanism of action]
Selective, systemic, absorbed by roots and translocated. Inhibition of lipid synthesis | [Pesticide Type]
Herbicide |
|
|