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                                  Flumioxazin

                                  English name:Flumioxazin
                                  Cas No. 103361-09-7
                                  Product Description:

                                  Information:

                                  IUPAC name : 2-[7-fluoro-3,4-dihydro-3-oxo-4-(2-propynyl)-2H-1,4-benzoxazin-6-yl]-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione

                                  Chemical formula: C19H15FN2O4

                                  Molecular mass (g mol-1) :354.33

                                  Physical state :White when pure (99.6%), yellow-brown powder (97.65)

                                  Properties :

                                  Melting point (°C) : 203.5

                                  Bulk density : 1.5 g/cm3

                                  Vapour pressure at 20°C (mPa):0.32

                                  Degradation point (°C) :273.3

                                  Solubility - In water at 20°C(mg l-1) :0.786

                                  Solubility - In organic solvents at 20°C (mg l-1) :Acetone:17000 ;Methanol:1600 ;Hexane :25;Ethyl acetate :17800

                                  ECOTOXICOLOGY

                                  Mammals - Acute oral LD50 (mg kg-1) :> 5000

                                  Mammals - Short term dietary NOEL(ppm diet):300

                                  Birds - Acute LD50 (mg kg-1):> 2250

                                  Birds - Short term dietary (LC50/LD50)> 500 ppm

                                  Fish - Chronic 21 day NOEC (mg l-1)0.37

                                  Fish - Acute 96 hour LC50 (mg l-1) :2.3

                                  Aquatic invertebrates - Acute 48 hour EC50 (mg l-1)5.9

                                  Aquatic invertebrates - Chronic 21 day NOEC (mg l-1)0.057

                                  Earthworms -Acute 14 day LC50 (mg kg-1)> 491

                                  Algae - Acute 72 hour EC50, growth (mg l-1)0.000852

                                  TOXICOLOGY

                                  Mammals - Acute oral LD50 (mg kg-1) > 5000 Rat

                                  Mammals - Dermal LD50 (mg kg-1 body weight) > 2000 Rat

                                  Mammals - Inhalation LC50 (mg l-1) > 3.93  Rat, 4 hr (nose only)

                                  ADI - Acceptable Daily Intake (mg kg-1bw day-1):  0.009 Mouse 

                                  ARfD - Acute Reference Dose (mg kg-1bw day-1):0.05

                                  Product description:

                                  Propyrazine is a protoporphyrinogen oxidase (PPO) inhibitor. In light and oxygen, it causes a large amount of accumulation of protoporphyrin in sensitive crops, which enhances the lipid peroxidation of the cell membrane, resulting in irreversible damage to the cell membrane structure and cell function of sensitive weeds. Propyrachlor is also a contact selective herbicide. After treating the surface layer of soil, the agent is absorbed by the soil particles and forms a treatment layer on the surface of the soil particles. After the weeds germinate, the seedlings die after contacting the treatment layer.

                                  Propyrachlor is used pre-emergence to control most annual broad-leaved weeds and some annual gramineous weeds in soybeans, peanuts, orchards, grapes and other crop fields, such as Commelina communis, P. chinensis, Xanthium sibiricum, Abutilon , Portulaca oleracea, Mustard petal flower, horse tang, etc., also have a certain inhibitory effect on barnyard grass, bristlegrass, golden bristlegrass, wild oats and endives. Propyrazine has a good control effect on the glyphosate weeds, which is becoming increasingly difficult to control-water hemp, and it has an excellent control effect on concentrated farming systems. The crops after the application of propaflux can choose to plant crops such as corn, wheat, barley, sorghum, alfalfa, dried bean, sugar beet and other crops.

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