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5-amino-3-cyano-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-1H-pyrazole-4-sulfonic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

209248-72-6

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209248-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209248-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,2,4 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 209248-72:
(8*2)+(7*0)+(6*9)+(5*2)+(4*4)+(3*8)+(2*7)+(1*2)=136
136 % 10 = 6
So 209248-72-6 is a valid CAS Registry Number.

209248-72-6Upstream product

209248-72-6Downstream Products

209248-72-6Relevant academic research and scientific papers

Kinetics and Mechanisms of Abiotic Degradation of Fipronil (Hydrolysis and Photolysis)

Bobe, Alain,Meallier, Pierre,Cooper, Jean-Francois,Coste, Camille M.

, p. 2834 - 2839 (1998)

The abiotic degradation of fipronil (compound I), a phenylpyrazole insecticide, was studied in aqueous solution and on the surface of two soils from Niger (Saguia and Banizoumbou) and one Mediterranean soil (Montpellier). The rate of hydrolysis of fipronil in solution was measured at different values of pH and temperature. The pH was an influencing factor: hydrolysis kinetics were pseudo-firstorder, the half-life being 770 h at pH 9.0, 114 h at pH 10.0, 11 h at pH 11.0, and 2.4 h at pH 12.0. Fipronil was stable under acid (pH 5.5) and neutral conditions. The Arrhenius relation was verified over the temperature range 22-45 °C: the activation energy was 62 kJ mol-1 and the calculated entropy change -32 J mol-1. Compound II [5-amino-3-carbamoyl-1-(2,6-dichloro-4-(trifluoromethyl)-phenyl)-4- [(trifluoromethyl)sulfinyl]pyrazole] was the only hydrolysis product detected. The hydrolysis reaction mechanism involves nucleophilic addition of OH- to the polar nitrile bond, producing a hydroxyimine which then undergoes tautomerization into an amide. Fipronil in acidic (pH 5.5) aqueous solution exposed to light from a xenon lamp degraded with first-order kinetics (Kobs, = 1.7 h-1) with concomitant appearance of 5-amino-3-cyano-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-4-(trifluoromethyl) pyrazole (compound III) and 5-amino-3-cyano-1-(2,6-dichloro-4-(trifluoromethyl)-phenyl)pyrazole-4-sulfonic acid (compound IV). The photolyte formation rate constants were 0.11 h-1 (III) and 0.05 h-1 (IV). The observed degradation process corresponded to a desulfinylation and an oxidation. The reaction mechanisms were not elucidated. The irradiation (xenon lamp) of fipronil adsorbed on three natural soils when dry led to the formation of 4-(trifluoromethyl)pyrazole (III). The Kobs values were 0.0047 h-1 (Saguia), 0.0039 h-1 (Banizoumbou), and 0.0032 h-1 (Montpellier). The degree of photodegradation was inversely proportional to fipronil adsorption: the Freundlich adsorption coefficients were, respectively, 4.3 (Saguia), 7.3 (Banizoumbou), and 45.5 (Montpellier).

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