Pure product is colorless translucent liquid, b.p.126℃/5.332Pa, relative density 1.107, m.p.22.5～23.8℃, refractive index n20D1.5106. easily soluble in many organic solvents, insoluble in water. Stable to light and acid, easy to decompose when meet alkaline material, industrial product is light yellow oily liquid.
Iprobenfos is a systemic fungicide which provides effective
protective and curative control of leaf and ear blast (Pyricularia oryzae),
stem rot (Helminthosporium spp.) and sheath blight (Rhizoctonia solani) in
rice.
ChEBI: An organic thiophosphate that is the S-benzyl O,O-diisopropyl ester of phosphorothioic acid. Used as a rice fungicide to control leaf and ear blast, stem rot and sheath blight.
The industrial production of iprobenfos involves the reaction of phosphorothioic acid with benzyl alcohol and isopropanol to form S-benzyl-O,O-diisopropyl phosphorothioate. This process typically includes controlled esterification under anhydrous conditions, followed by purification steps such as distillation or crystallisation to achieve high purity.
Systemic, with both curative and protective properties. Absorbed through roots and translocated. Phospholipid biosynthesis inhibitor
Iprobenfos undergoes extensive degradation and metabolism. Primary
metabolic pathways include isomerisation to the thionate (P=S) ester,
cleavage of the P-S-benzyl and P-O-isopropyl moieties, and transesterification.
Benzyl mercaptan, upon cleavage, undergoes additional
oxidation reactions to yield the alcohol, carboxylic acid, disulfide and
sulfonic acid. The formation of the oxon from the isomerisation product
(P=S ester) was minor and was observed only under UV light irradiation.
The primary metabolic pathways of iprobenfos are presented in
Scheme 1.
Iprobenfos (1) is stable to hydrolytic degradation (<50 °C). The DTN
value of iprobenfos in aqueous solution was approximately 301-324 days(PM).
Iprobenfos degraded rapidly when deposited as a thin film and
exposed to UV light (DT50 ca. 10 min). Two major degradation reactions
were observed during the initial phase of the irradiation. The first reaction
involved the isomerisation of iprobenfos to O,O-diisopropyl O-
benzyl phosphorothioate (2) followed by the oxidative desulfuration
of compound 2 to yield the corresponding oxon analogue 3 (O,O-diisopropyl
O-benzyl phosphate). The second reaction involved the
hydrolytic cleavage of the S-C linkage of iprobenfos to yield O,O-diisopropyl
hydrogen phosphorothioate (4) and the cleavage of the
P-O-benzyl linkage of compound 3 to yield O,O-diisopropyl hydrogen
phosphate (5). Other major photolytic degradation reactions include the
cleavage of the parent P-S linkage to O,O-diisopropyl phosphonate (6).
Benzyl alcohol (7) and benzyl mercaptan (8) were also detected. Further
oxidation of compound 7 yielded benzoic acid (9) and the oxidation
of compound 8 yielded benzylsulfonic acid (10), dibenzyl disulfide (11)
and sulfuric acid as terminal products. Other minor products detected
included transesterification products [O,O,S-triisopropyl phosphorothioate
(12), O,O,O-triisopropyl phosphate (13)] and benzyl isopropyl
sulfide (14).
