Structure via PubChem · Public domain (PubChem)
binapacryl
Sign in to saveBinapacryl was used as a miticide and fungicide. Chemically, it is an ester derivative of dinoseb. Although binapacryl has low toxicity itself, it is readily metabolized to form dinoseb, which is highly toxic.
Chemical data
- Formula
- C15H18N2O6
- Molecular weight
- 322.31 g/mol
- IUPAC name
- (2-butan-2-yl-4,6-dinitrophenyl) 3-methylbut-2-enoate
- SMILES
- CCC(C)C1=C(C(=CC(=C1)[N+](=O)[O-])[N+](=O)[O-])OC(=O)C=C(C)C
- InChIKey
- ZRDUSMYWDRPZRM-UHFFFAOYSA-N
- XLogP
- 4.6
- Polar surface area
- 118 Ų
- H-bond donors
- 0
- H-bond acceptors
- 6
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 322.116
- Has use
- fungicide
Show 3 more facts
- Commons category
- Binapacryl
- chemical formula
- C₁₅H₁₈N₂O₆
- canonical SMILES
- CCC(C)C1=CC(=CC(=C1OC(=O)C=C(C)C)[N+](=O)[O-])[N+](=O)[O-]
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Binapacryl was used as a miticide and fungicide. Chemically, it is an ester derivative of dinoseb. Although binapacryl has low toxicity itself, it is readily metabolized to form dinoseb, which is highly toxic.
International trade in binapacryl is regulated by the Rotterdam Convention; it has been withdrawn as a pesticide, since products were highly toxic to mammals, fish and aquatic invertebrates.
Excerpted from Wikipedia’s “binapacryl” article, available under the CC BY-SA 4.0 licence.
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