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1716-09-2

1716-09-2 Structure

1716-09-2 Structure
IdentificationBack Directory
[Name]

FENTHION-ETHYL
[CAS]

1716-09-2
[Synonyms]

lucijet
om-1455
B-29492
bay29492
ent25,636
bayer29492
bayers1751
ethylfenthion
FENTHION-ETHYL
O,O-diethyl O-[3-methyl-4-(methylthio)phenyl] thiophosphate
o,o-diethylo-(3-methyl-4-(methylthio)phenyl)phosphorothioate
phosphorothioicacid,o,o-diethylo-(4-(methylthio)-m-tolyl)ester
Thiophosphoric acid O,O-diethyl O-(4-methylthio-m-tolyl) ester
phosphorothioicacid,o,o-diethylo-(3-methyl-4-(methylthio)phenyl)ester
[EINECS(EC#)]

216-999-3
[Molecular Formula]

C12H19O3PS2
[MDL Number]

MFCD01704910
[MOL File]

1716-09-2.mol
[Molecular Weight]

306.381
Chemical PropertiesBack Directory
[EPA Substance Registry System]

Phosphorothioic acid, O,O-diethyl O-[3-methyl-4-(methylthio)phenyl] ester (1716-09-2)
Safety DataBack Directory
[Symbol(GHS) ]

Environment (GHS09)Skull and Crossbones (GHS06)
GHS09,GHS06
[Signal word ]

Danger
[Hazard statements ]

H300+H330-H311-H410
[Precautionary statements ]

P273-P391-P501-P280-P302+P352-P312-P322-P361-P363-P405-P501
Hazard InformationBack Directory
[Production Methods]

Fenthion-ethyl was produced by adapting the standard organophosphorothioate assembly used across the fenthion family. Commercial manufacture began with preparation of the phosphorothiochloridate intermediate, generated from inexpensive phosphorus trichloride and sulphur chemistry under controlled conditions. This activated phosphorus species was then reacted with the appropriate ethyl-substituted thioether alcohol to form the O-alkyl phosphorothioate framework that defines fenthion-ethyl. Producers focused on achieving clean substitution at phosphorus, managing sulphur-based impurities, and purifying the resulting ester to technical grade suitable for formulation.
[Mechanism of action]

Acetylcholinesterase (AchE) inhibitor.
[Pesticide Type]

Insecticide
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