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Iodofenphos

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Iodofenphos Basic information
Product Name:Iodofenphos
Synonyms:JODFENPHOS;JODFENPHOS(R);NUVANOL(R) N;O-2,5-DICHLORO-4-IODOPHENYL-O,O-DIMETHYLPHOSPHOROTHIOATE;3,4-dichloro-phenoo-esterwitho-methylmethylphosphoramidothioate;C 9491;monocron9491;NSC 190998
CAS:18181-70-9
MF:C8H8Cl2IO3PS
MW:413
EINECS:242-069-1
Product Categories:JPesticides;Alpha sort;Alphabetic;H-MAnalytical Standards;Insecticides;Organophorous;Pesticides&Metabolites
Mol File:18181-70-9.mol
Iodofenphos Structure
Iodofenphos Chemical Properties
Melting point 72-73° (Beriger); mp 75° (Haddow)
Boiling point 30.1°C
density 2.0 g/cm3
storage temp. APPROX 4°C
form solid
Water Solubility 0.1mg/L(20 ºC)
Merck 13,5054
Henry's Law Constant2.2×100 mol/(m3Pa) at 25℃, HSDB (2015)
Major Applicationagriculture
environmental
InChI1S/C8H8Cl2IO3PS/c1-12-15(16,13-2)14-8-4-5(9)7(11)3-6(8)10/h3-4H,1-2H3
InChIKeyLFVLUOAHQIVABZ-UHFFFAOYSA-N
SMILESCOP(=S)(OC)Oc1cc(Cl)c(I)cc1Cl
EPA Substance Registry SystemJodfenphos (18181-70-9)
Safety Information
Hazard Codes Xn,N
Risk Statements 21-50/53
Safety Statements 36/37-60-61
RIDADR UN2811 6.1/PG 3
WGK Germany WGK 3
RTECS TF0175000
HS Code 29201900
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Dermal
Aquatic Acute 1
Hazardous Substances Data18181-70-9(Hazardous Substances Data)
ToxicityLD50 in rats, female mice (mg/kg): 2100, >10000, orally (Haddow, Marks)
MSDS Information
Iodofenphos Usage And Synthesis
UsesInsecticide.
UsesJodfenphos is lavendustin A.
DefinitionChEBI: Iodofenphos is an organic thiophosphate.
Production MethodsIodofenphos is produced through a targeted esterification process. The synthesis begins with O,O-dimethylthiophosphoryl chloride, which reacts with 2,5-dichloro-4-iodophenol sodium salt. This reaction typically occurs in an organic solvent like dichloromethane or benzene under controlled temperature and stirring conditions. The thiophosphoryl chloride acts as the electrophilic agent, forming a phosphorothioate ester bond with the phenolic component. After the reaction is complete, the mixture is purified through filtration, solvent extraction, and crystallization, yielding iodofenphos.
Mechanism of actionContact and stomach action with long lasting effects. Acetylcholinesterase (AchE) inhibitor.
Pesticide TypeInsecticide; Acaricide; Veterinary substance
Iodofenphos Preparation Products And Raw materials
Tag:Iodofenphos(18181-70-9) Related Product Information
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