A chitin synthesis inhibitor
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Hexaflumuron

Item No. 18598

Technical Information
Formal Name
N-[[[3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl]amino]carbonyl]-2,6-difluoro-benzamide
CAS Number
86479-06-3
Synonyms
  • AI-3-29832
  • OMS-3031
  • XRD-473
Molecular Formula
C16H8Cl2F6N2O3
Formula Weight
Purity
≥95%
Formulation
A crystalline solid
DMF: 10 mg/mlDMSO: 10 mg/mlDMSO:PBS(pH 7.2) (1:2): 0.3 mg/ml
λmax
209, 254 nm
SMILES
FC1=C(C(NC(NC2=CC(Cl)=C(OC(F)(F)C(F)F)C(Cl)=C2)=O)=O)C(F)=CC=C1
InChi Code
InChI=1S/C16H8Cl2F6N2O3/c17-7-4-6(5-8(18)12(7)29-16(23,24)14(21)22)25-15(28)26-13(27)11-9(19)2-1-3-10(11)20/h1-5,14H,(H2,25,26,27,28)
InChi Key
RGNPBRKPHBKNKX-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Hexaflumuron is a chitin synthesis inhibitor used to bait and eliminate termite colonies.1 Hexaflumuron spreads efficiently through entire populations through mutual exchange of liquids via regurgitation.2 Termites are unable to metabolize hexaflumuron and clearance is slow, resulting in up to 100% elimination. Hexaflumuron has also been tested for use with the raisin moth, cowpea weevil, and Asiatic rice borer with positive results.3,4 Formulations containing hexaflumuron have been used in the control of insects in residential areas.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Evans, T.A., and Igbal, N. Termite (order Blattodea, infraorder Isoptera) baiting 20 years after commercial release. Pest. Manag. Sci. 71(7), 897-906 (2015).

    2. Sheets, J.J., Karr, L.L., and Dripps, J.E. Kinetics of uptake, clearance, transfer, and metabolism of hexaflumuron by eastern subterranean termites (Isoptera: Rhinotermitidae). J. Econ. Entomol. 93(3), 871-877 (2000).

    3. Khajepour, S., Izadi, H., and Asari, M.J. Evaluation of two formulated chitin synthesis inhibitors, hexaflumuron and lufenuron against the raisin moth, Ephestia figulilella. J. Insect. Sci. 12, 102 (2012).

    4. Abo-Elghar, G.E., El-Sheikh, A.E., El-Sayed, F.M., et alPersistence and residual activity of an organophosphate, pirimiphos-methyl, and three IGRs, hexaflumuron, teflubenzuron and pyriproxyfen, against the cowpea weevil, Callosobruchus maculatus (Coleoptera: Bruchidae). Pest. Manag. Sci. 60(1), 95-102 (2004).