Binapacryl

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Binapacryl[1]
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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
485-31-4 N
ChEBI CHEBI:82153 N
ChemSpider 9817 YesY
Jmol 3D model Interactive image
KEGG C19022 N
PubChem 10234
UNII 4X685BB13A YesY
  • 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 YesY
    Key: ZRDUSMYWDRPZRM-UHFFFAOYSA-N YesY
  • 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
  • O=C(Oc1c(cc(cc1C(C)CC)[N+]([O-])=O)[N+]([O-])=O)\C=C(/C)C
Properties
C15H18N2O6
Molar mass 322.32 g·mol−1
Density 1.2 g/cm3
Melting point 66 to 67 °C (151 to 153 °F; 339 to 340 K)
Insoluble
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
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

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  1. 1.0 1.1 Datasheet from International Programme on Chemical Safety
  2. Binapacryl at alanwood.net