Oxabetrinil
Structural formula | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
![]() |
||||||||||
General | ||||||||||
Surname | Oxabetrinil | |||||||||
other names |
|
|||||||||
Molecular formula | C 12 H 12 N 2 O 3 | |||||||||
Brief description |
colorless crystals |
|||||||||
External identifiers / databases | ||||||||||
|
||||||||||
properties | ||||||||||
Molar mass | 232.24 g mol −1 | |||||||||
Physical state |
firmly |
|||||||||
Melting point |
77.7 ° C |
|||||||||
solubility |
practically insoluble in water (0.02 g l −1 at 20 ° C) |
|||||||||
safety instructions | ||||||||||
|
||||||||||
Toxicological data | ||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Oxabetrinil is a chemical compound from the group of oxime ethers and a herbicide safener introduced by Ciba-Geigy in 1982 .
use
Oxabetrinil is at different Sorghum as mordant applied to the plant against damage by the herbicide metolachlor preserve. The active ingredient stimulates the breakdown of metolachlor by glutathione-S-transferase . Oxabetrinil has been replaced by fluxofenim .
Individual evidence
- ↑ a b c d e f Entry on Oxabetrinil. In: Römpp Online . Georg Thieme Verlag, accessed on March 5, 2014.
- ↑ a b Oxabetrinil data sheet from Sigma-Aldrich , accessed on May 21, 2017 ( PDF ).