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| | CYCLOXYDIM Basic information |
| | CYCLOXYDIM Chemical Properties |
| Melting point | 41℃ | | Boiling point | 455.7±55.0 °C(Predicted) | | density | 1.21 | | storage temp. | -20°C | | solubility | Chloroform (Slightly), Methanol (Slightly) | | pka | 4.32±0.25(Predicted) | | color | White to Pale Yellow | | BRN | 8436332 | | Stability: | Hygroscopic | | Major Application | agriculture
environmental | | InChI | 1S/C17H27NO3S/c1-3-6-14(18-21-4-2)17-15(19)9-13(10-16(17)20)12-7-5-8-22-11-12/h12-13,19H,3-11H2,1-2H3/b18-14+ | | InChIKey | GGWHBJGBERXSLL-NBVRZTHBSA-N | | SMILES | CCC\C(=N/OCC)C1=C(O)CC(CC1=O)C2CCCSC2 |
| Hazard Codes | F,Xi,Xn | | Risk Statements | 11-36-66-67-63 | | Safety Statements | 9-16-26 | | RIDADR | UN 1090 3/PG 2 | | WGK Germany | 3 | | RTECS | GW6425000 | | HS Code | 29349990 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Repr. 2 |
| | CYCLOXYDIM Usage And Synthesis |
| Uses | Cycloxydim is a cyclohexene oxime herbicide that is used for the control of grass weeds of many agricultural and horticultural broad-leaved crops. | | Definition | ChEBI: A beta-diketone that is cyclohexa-1,3-dione which is substituted at position 2 by an N-ethoxybutanimidoyl group and at position 5 by a tetrahydro-2H-thiopyran-3-yl group. A systemic herbicide effective
against grasses, it is used in the cultivation of a variety of crops, including oil seed rape and potatoes. | | Metabolic pathway | Cycloxydim is rapidly metabolized in soybean plants,
and four series of different types of metabolite in either
free or conjugated form are identified. Transformation
products are formed by chemical and/or enzymatic
reactions involving a range of oxidation, a
rearrangement, and cleavage of the cyclohexanone
ring or ethoxyimino side chain. |
| | CYCLOXYDIM Preparation Products And Raw materials |
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