Binapacryl

Binapacryl^[1]
Names
	IUPAC name (RS)-(2-Butan-2-yl-4,6-dinitrophenyl) 3-methylbut-2-enoate
	Other names Dapacryl; Morocide; Morrocid; Acricid; Endosan; Ambox; Dinoseb methacrylate
Identifiers
CAS Number	485-31-4 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:82153 ;
ChemSpider	9817 ;
ECHA InfoCard	100.006.921
KEGG	C19022 ;
PubChem CID	10234;
UNII	4X685BB13A ;
CompTox Dashboard (EPA)	DTXSID9040269 ;
	InChI InChI=1S/C15H18N2O6/c1-5-10(4)12-7-11(16(19)20)8-13(17(21)22)15(12)23-14(18)6-9(2)3/h6-8,10H,5H2,1-4H3 Key: ZRDUSMYWDRPZRM-UHFFFAOYSA-N ; InChI=1/C15H18N2O6/c1-5-10(4)12-7-11(16(19)20)8-13(17(21)22)15(12)23-14(18)6-9(2)3/h6-8,10H,5H2,1-4H3 Key: ZRDUSMYWDRPZRM-UHFFFAOYAH;
	SMILES O=C(Oc1c(cc(cc1C(C)CC)[N+]([O-])=O)[N+]([O-])=O)\C=C(/C)C;
Properties
Chemical formula	C15H18N2O6
Molar mass	322.317 g·mol−1
Density	1.2 g/cm3
Melting point	66 to 67 °C (151 to 153 °F; 339 to 340 K)
Solubility in water	Insoluble
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Binapacryl is an miticide and fungicide.^[2] Chemically, it is an ester derivative of dinoseb. Although binapacryl has low toxicity itself, it is readily metabolized to form dinoseb, which is toxic.^[1]

International trade in binapacryl is regulated by the Rotterdam Convention.

References

^ ^a ^b Datasheet from International Programme on Chemical Safety
^ Binapacryl at alanwood.net

[inchem-1] Datasheet from International Programme on Chemical Safety

[2] Binapacryl at alanwood.net

[1]

[2]