SULFENTRAZONE
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- CAS-Nr.
- 122836-35-5
- Englisch Name:
- SULFENTRAZONE
- Synonyma:
- N-(2,4-dichloro-5-(4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl)phenyl)methanesulfonamide;BORAL;CAPAZ;f6285;FMC97285;AUTHORITY;SULFENTRAZONE;Sulfentrazonel;Sulfentrazone standard;SULFENTRAZONE,FMC 97285
- CBNumber:
- CB7677780
- Summenformel:
- C11H10Cl2F2N4O3S
- Molgewicht:
- 387.19
- MOL-Datei:
- 122836-35-5.mol
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SULFENTRAZONE Eigenschaften
- Schmelzpunkt:
- 75-78°
- Siedepunkt:
- 468.2±55.0 °C(Predicted)
- Dichte
- 1.21 g/cm3
- storage temp.
- 0-6°C
- L?slichkeit
- Chloroform (Slightly), Methanol (Slightly)
- pka
- 6.56(at 25℃)
- Aggregatzustand
- Solid
- Farbe
- Pale Brown to Beige
- EPA chemische Informationen
- Sulfentrazone (122836-35-5)
SULFENTRAZONE Chemische Eigenschaften,Einsatz,Produktion Methoden
Beschreibung
Solubility. In water at 25 ?C: 100 mg/L at pH 6,
800 mg/mL at pH 7, 1,600 mg/mL at pH 7.5; soluble to
some extent in acetone and other polar organic solvents
Pka. 6.56
Stability. Stable
Verwenden
Sulfentrazone is an herbicide used for controlling sedges in turfgrass.
Handelsname
AUTHORITY® Sulfentrazone; CANOPY XL®; COVER®; F6285®; FMC® 97285; GAUNTLET®; SPARTAN®; SULFENTRAZONE® (F6285) 4F; SULFENTRAZONE® (F6285) 75DF
Stoffwechselwegen
When 14C-sulfentrazone is applied to coffee senna
and sicklepod through the roots, 83% of the parent
compound remains in coffee senna leaf tissue after
9 h exposure and in contrast, sicklepod takes up
relatively less sulfentrazone through the root and
metabolizes sulfentrazone in the foliage more rapidly
than coffee senna. The primary detoxification reaction
appears to be oxidation of the methyl group on the
triazolinone ring, resulting in the formation of the more
polar hydroxymethyl derivative. The aniline analog is
identified as a plant-specific metabolite. The tolerance
of sicklepod to sulfentrazone is primarily due to a
relatively high rate of metabolism of sulfentrazone
compared with coffee senna. When 14C-sulfentrazone
is administered orally to rats, goats, and hens in a
daily diet, administered radioactivity is quantitatively
excreted in the urine, feces, or hen excreta. In all of
the species, unchanged sulfentrazone and two non-conjugated metabolites are found, which are 3-hydroxymethyl and carboxylic acid derivatives, the
latter of which decomposes at high temperature or
acidic pH to give the corresponding desmethyl analog
of sulfentrazone. In rats, a minor reduction metabolite
is detected which is tentatively characterized as the
2,3-dihydro-3-hydroxymethyl derivative.
SULFENTRAZONE Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
SULFENTRAZONE Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.
Global( 161)Lieferanten
122836-35-5()Verwandte Suche:
- 2′,4′-dichloro-5′-(4-difluoromethyl-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl)methanesulfonanilide
- SULFENTRAZONE,FMC 97285
- Methanesulfonamide, N-2,4-dichloro-5-4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-ylphenyl-
- 2',4'-dichloro-5'-(4-difluoromethyl-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl) methanesulfonanilide
- Sulfentrazone standard
- N-(2,4-dichloro-5-(4-(difluoroMethyl)-3-Methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)phenyl)MethanesulfonaMide
- FREE SAMPLE NCV SULFENTRAZONE TECHNICAL
- SULFENTRAZONE
- CAPAZ
- BORAL
- AUTHORITY
- 4-triazol-1-yl)phenyl)-5-oxo-1h-2
- f6285
- FMC97285
- n-(2,4-dichloro-5-(4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1h-1,2,4-triazol-1-yl)phenyl)-methanesulfonamid
- n-(2,4-dichloro-5-(4-(difluoromethyl)-4,5-dihydro-3-methyl-methanesulfonamid
- Sulfentrazone@1000 μg/mL in Acetonitrile
- Sulfentrazone100 μg/mL in Acetonitrile
- Sulfentrazonel
- SULFENTRAZONE ISO 9001：2015 REACH
- N-(2,4-dichloro-5-(4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl)phenyl)methanesulfonamide
- C17000300 Sulfentrazone
- L17000300ALSulfentrazonE10μg/mLin Acetonitr
- Sulfentrazone 10.0 μg/ml Acetonitrile
- Sulfentrazone 10.0 μg/ml Ethyl acetate
- Sulfentrazone in Acetonitrile
- 122836-35-5
- C11H10Cl2F2N4O3S
