| Identification | Back Directory | [Name]
BUTROXYDIM | [CAS]
138164-12-2 | [Synonyms]
FALCON
Fenoxydim
BUTROXYDIM
Butroxydim [iso]
butroxydim (bsi, pa e-iso)
ZOGDSYNXUXQGHF-XIEYBQDHSA-N
Butroxydim@100 μg/mL in Methanol
Butroxydim, 10 μg /μL in cyclohexane
5-(3-butyryl-2,4,6-trimethylphenyl)-2-[1-(ethoxyimino)propyl]-3-hydroxycyclohex-2-en-1-one
2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-[2,4,6-trimethyl-3-(1-oxobutyl)phenyl]-2-cyclohexen-1-one
2-Cyclohexen-1-one, 2-[1-(ethoxyimino)propyl]-3-hydroxy-5-[2,4,6-trimethyl-3-(1-oxobutyl)phenyl]- | [EINECS(EC#)]
414-790-3 | [Molecular Formula]
C24H33NO4 | [MDL Number]
MFCD04112609 | [MOL File]
138164-12-2.mol | [Molecular Weight]
399.52 |
| Chemical Properties | Back Directory | [Melting point ]
80.8℃ | [Boiling point ]
535.9±60.0 °C(Predicted) | [density ]
1.11±0.1 g/cm3(Predicted) | [storage temp. ]
0-6°C | [pka]
4.18±0.25(Predicted) | [Henry's Law Constant]
1.7×104 mol/(m3Pa) at 25℃, MacBean (2012) |
| Hazard Information | Back Directory | [Description]
Butroxydim is an obsolete herbicide. It has a low aqueous solubility, is relatively volatile and, based on its chemical properties, is non-mobile and would not be expected to leach to groundwater. It is generally non-persistent in soil systems but may persist in aquatic systems under certain conditions. It is not generally susceptible to hydrolysis. It has a moderate mammalian toxicity and has a high potential to bioaccumulate. It is moderately toxic to most aquatic species, birds and earthworms but relatively non-toxic to honeybees. | [Definition]
ChEBI: Butroxydim is a butanone. | [Production Methods]
The production of butroxydim involves synthesising a cyclohexane-1,3-dione core, which serves as the backbone for its herbicidal activity. The process begins with constructing the substituted aromatic ring, typically a 3-butanoyl-2,4,6-trimethylphenyl group, through Friedel–Crafts acylation and methylation reactions. This aromatic moiety is then coupled to the cyclohexanedione ring via condensation, forming a stable enone intermediate. Next, the key oxime ether side chain is introduced by reacting the enone with ethoxyamine, yielding the biologically active ketoxime structure. | [Mechanism of action]
Selective and systemic. Absorbed by leaves and translocated. Acetyl CoA carboxylase inhibitor (ACCase) - distrupts fatty acid biosynthesis and lipid formation. | [Pesticide Type]
Herbicide |
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| Company Name: |
Wuhan Topule
|
| Tel: |
+86-02787215551 19945035818 |
| Website: |
http://www.topule.com/ |
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