| Identification | More | [Name]
Oryzaemate | [CAS]
27605-76-1 | [Synonyms]
ALLYLOXY-1,2-BENZ[D]ISOTHIAZOLE-1,1-DIOXIDE
ORYZAMATE(R)
ORYZEMATE
PROBENAZOLE
1,2-benzisothiazole,3-(2-propenyloxy)-,1,1-dioxide
1,2-benzisothiazole,3-(allyloxy)-,1,1-dioxide
3-(2-propenyloxy)-1,2-benzisothiazole1,1-dioxide
3-(allyloxy)-1,2-benzisothiazole1,1-dioxide
oryzaemate
po-20
PROBENAZOIE
probenazole (jmaf)
ORYZAMATE
3-Allyloxy-1,2-benzoisothiazole 1,1-dioxide | [Molecular Formula]
C10H9NO3S | [MDL Number]
MFCD00274602 | [Molecular Weight]
223.25 | [MOL File]
27605-76-1.mol |
| Chemical Properties | Back Directory | [Melting point ]
136～141℃ | [Boiling point ]
220°C (rough estimate) | [density ]
1.3588 (rough estimate) | [vapor pressure ]
5 x 10-4 Pa (20 °C) (est.) | [refractive index ]
1.6500 (estimate) | [storage temp. ]
0-6°C | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
-2.43±0.20(Predicted) | [Water Solubility ]
150 mg l-1 | [color ]
White to Off-White | [CAS DataBase Reference]
27605-76-1(CAS DataBase Reference) | [NIST Chemistry Reference]
Probenazole(27605-76-1) |
| Hazard Information | Back Directory | [Uses]
Probenazole can be used in agricultural use and biological study of preparation of nicotinamide compounds containing chiral oxazoline and application thereof as agricultural antimicrobial agent. | [Uses]
Probenazole is used for the control of rice blast and bacterial
diseases in paddy rice. | [Definition]
ChEBI: A member of the class of 1,2-benzothiazoles that is 1,2-benzothiazole 1,1-dioxide substituted at position 3 by an allyloxy group. A fungicide used to control rice blast. | [Production Methods]
Probenazole is industrially produced starting from saccharin (1,2-benzisothiazolin-3-one 1,1-dioxide). The key steps involve chlorination of saccharin with thionyl chloride in the presence of catalysts like dioxane and DMF to form saccharin chloride (pseudosaccharyl chloride). This intermediate is then concentrated and undergoes etherification with allyl alcohol in dichloromethane (or similar solvent) to introduce the allyloxy group at the 3-position. The resulting crude probenazole is purified through pH adjustment, washing, drying, and grinding (or milling) to yield the final technical-grade product suitable for formulation. | [Mechanism of action]
Induces systemic acquired resistence - plant defense activator | [Metabolic pathway]
Probenazole is metabolised readily in plants by hydrolytic ring opening
followed by a cyclisation-induced dealkylation to form saccharin which
is N-glucosylated. Saccharin may be the active metabolite of probenazole.
No information on the fate of probenazole in soil or animals could
be located. | [Metabolism]
Probenazole is taken up by the rice plants after spray or paddy application and distributed
throughout the plants as parent compound or as one of its
metabolites . The main metabolites of probenazole
in rice are 2-sulfamoyl-allyl-benzoate, saccharin, and N-β-
D-glucopyranosylsaccharin (37). | [Degradation]
Probenazole is a stable compound but it is subject to hydrolysis. | [Pesticide Type]
Fungicide |
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