|Status:||ISO 1750 (published)|
|Activity:||rodenticides (coumarin rodenticides)|
|Notes:||When the name bromadiolone was approved, no information on the proportions of the 4 stereoisomers was provided, and the name has been assumed to apply to any mixture of stereoisomers. It is now known that bromadiolone has always comprised a mixture of ≥ 80% (1RS,3SR)-isomer and ≤ 20% (1RS,3RS)-isomer, and the definition will be updated when ISO 1750 is revised.
The mixture of ≥ 80% (1RS,3RS)-isomer and ≤ 20% (1RS,3SR)-isomer has its own ISO common names, alpha-bromadiolone
|Pronunciation:||brō-ma-dī-ō-lōn Guide to British pronunciation|
|InChIKey:||LQAGAOMQXARIFO-YORONTHLSA-N (major component)|
|InChI:||InChI=1S/2C30H23BrO4/c2*31-23-16-14-20(15-17-23)19-10-12-22(13-11-19)26(32)18-25(21-6-2-1-3-7-21)28-29(33)24-8-4-5-9-27(24)35-30(28)34/h2*1-17,25-26,32-33H,18H2/t2*25-,26+/m10/s1 (major component)|
A data sheet from the Compendium of Pesticide Common Names