CAS No.: | 103361-09-7 |
---|---|
Formula: | C19h15fn2o4 |
EINECS: | 103361-09-7 |
Appearance: | Powder |
Method of Application: | Cauline Leaf, Soil Treatment Agent |
Usage: | Selective |
Samples: |
---|
Customization: |
---|
Suppliers with verified business licenses
Product Name: | FLUMIOXAZIN |
Synonyms: | 7-fluoro-6-(3,4,5,6-tetrahydrophthalimido)-4-(2-propynyl)-1,4-benzoxazin-3(2;sumisoya;1H-Isoindole-1,3(2H)-dione, 2-7-fluoro-3,4-dihydro-3-oxo-4-(2-propynyl)-2H-1,4-benzoxazin-6-yl-4,5,6,7-tetrahydro-;flumioxazin (bsi, draft iso, ansi);FLUMIOXAZIN STANDARD;flumioxazin (ISO) N-(7-fluoro-3,4-dihydro-3-oxo-4-prop-2-ynyl-2H-1,4-benzoxazin-6-yl)cyclohex-1-ene-1,2-dicarboxamide;N-(7-fluoro-3,4-dihydro-3-oxo-4-prop-2-ynyl-2H-1,4-benzoxazin-6-yl)cyclohex-1-ene-1,2-dicarboxamide ,flumioxazin (ISO);Flumioxazin Solution, 1000ppm |
CAS: | 103361-09-7 |
MF: | C19H15FN2O4 |
MW: | 354.33 |
EINECS: | |
Product Categories: | Agro-Products;Aromatics;Heterocycles |
Mol File: | 103361-09-7.mol |
FLUMIOXAZIN Chemical Properties |
Melting point | 201.83-203.83° |
Boiling point | 644.4±55.0 °C(Predicted) |
density | d20 1.5132 g/ml |
storage temp. | 0-6°C |
form | neat |
pka | -0.01±0.20(Predicted) |
EPA Substance Registry System | Flumioxazin (103361-09-7) |
Safety Information |
Hazard Codes | T,N |
Risk Statements | 61-50/53 |
Safety Statements | 53-45-60-61 |
RIDADR | UN 3077 9 / PGIII |
WGK Germany | 3 |
Toxicity | LD50 in rats (mg/kg): >5000 orally; >2000 dermally; LC50 (4 hr) in rats (mg/m3): >3930 by inhalation; LC50 (96 hr) in bluegill, rainbow trout (mg/l): >21, 2.3 (Yoshida). |
MSDS Information |
FLUMIOXAZIN Usage And Synthesis |
Description | FLUMIOXAZIN is a benzoxazinones-type herbicide used on soybeans, peanuts, orchard fruits and other crop. It is a diphenyl ether group G herbicide that functioning through inhibiting the protoorphyrinogen oxidase. As a light-dependent peroxidising herbicide (LDPH), it takes effect by blocking heme and chlorophyll biosynthesis resulting in the accumulation of phototoxic porphyrins, leading to the membrane damage and further killing the weeds. |
Uses | Herbicide. |
Metabolic pathway | When the rats are given a single oral dose of 14C-S- 53482, seven metabolites are identified in the urine and the feces. Alcohol derivatives and the acetoanilide derivative are isolated from the urine, and three sulfonic acid conjugates with a sulfonic acid group incorporated into the double bond of the 3,4,5,6- tetrahydrophthalimide moiety are isolated from the feces. |
Suppliers with verified business licenses