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| FLUMICLORAC-PENTYL Basic information |
| Product Name: | FLUMICLORAC-PENTYL | | Synonyms: | SUMIVERDE;RESOURCE;FLUMICLORAC-PENTYL;flumiclorac-pentyl (bsi,pa iso,ansi);PENTYL2-CHLORO-4-FLUORO-5-(3,4,5,6-TETRAHYDROPHTHALIMIDO)PHENOXYACETATE;PENTYL2-CHLORO-4-FLUORO-5-(3,4,5,6-TETRAHYDROPHTHALIMIDO).;pentyl-[2-chloro-5-(cyclohex-1-ene-1,2-dicarboxamido)-4-fluorophenoxy] acetate;S 23031 | | CAS: | 87546-18-7 | | MF: | C21H23ClFNO5 | | MW: | 423.86 | | EINECS: | | Product Categories: | | Mol File: | 87546-18-7.mol |
| FLUMICLORAC-PENTYL Chemical Properties |
| Melting point | 90-91℃ | | Boiling point | 558.0±50.0 °C(Predicted) | | density | d20 1.3316 | | storage temp. | 0-6°C | | pka | -2.32±0.20(Predicted) | | EPA Substance Registry System | Flumiclorac-pentyl (87546-18-7) |
| HS Code | 29251900 | | Toxicity | LD50 in rats (mg/kg): >5000 orally; >2000 dermally (Kamoshita) |
| FLUMICLORAC-PENTYL Usage And Synthesis |
| Uses | Herbicide. | | Uses | Flumiclorac-pentyl is a herbicide. | | Metabolic pathway | In the feces and urine of rats, more than 90% of
administered 14C-flumiclorac pentyl is excreted within
48 h of treatment. Flumiclorac pentyl is rapidly and
extensively metabolized. The major fecal metabolites
are identified as the sulfonic acid conjugates, and the
major urinary metabolite is identified as 5-amino-2-
chloro-4-fluorophenoxyacetic acid. The metabolic
reactions include cleavage of the ester linkage, cleavage
of the imide linkage, hydroxylation and following
reduction at the cyclohexene ring of the cyclohexene-
1,2-dicarboxylic acid moiety, and incorporation of a
sulfonic acid group into the carbon ? carbon double bond
of the 3,4,5,6-tetrahydrophthalimide moiety. |
| FLUMICLORAC-PENTYL Preparation Products And Raw materials |
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