Bromopropylate
Names | |
---|---|
Preferred IUPAC name Propan-2-yl bis(4-bromophenyl)hydroxyacetate | |
Other names Acarol; Isopropyl 4,4'-dibromobenzilate; Phenisobromolate | |
Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
ChemSpider |
|
ECHA InfoCard | 100.038.231 |
PubChem CID |
|
UNII |
|
CompTox Dashboard (EPA) |
|
InChI
| |
| |
Properties | |
Chemical formula | C17H16Br2O3 |
Molar mass | 428.120 g·mol−1 |
Appearance | White solid[1] |
Density | 1.59 g/cm3 (20 °C)[1] |
Melting point | 77 °C (171 °F; 350 K)[1] |
Solubility in water | 0.1 mg/L (20 °C)[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references |
Chemical compound
Bromopropylate is a chemical compound used as an acaricide against spider mites in apiaries and on fruit crops such as citrus and grapes.[1] It was banned by the European Union in 2011.
Preparation
Bromopropylate is prepared by the esterification of the 4,4'-dibromo derivative of benzilic acid with isopropanol.
References
- ^ a b c d e Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health