Fluvalinate

Chemical compound
  • QP53AC10 (WHO)
Identifiers
  • [Cyano-(3-phenoxyphenyl)methyl] 2-[2-chloro-4-(trifluoromethyl)anilino]-3-methylbutanoate
CAS Number
  • 69409-94-5 ☒N
    102851-06-9 (tau-fluvalinate)
PubChem CID
  • 50516
ChemSpider
  • 45805 ☒N
UNII
  • 364G5G03VC
KEGG
  • C10989 checkY
ChEBI
  • CHEBI:5135
ChEMBL
  • ChEMBL3185183
CompTox Dashboard (EPA)
  • DTXSID7024110 Edit this at Wikidata
ECHA InfoCard100.233.047 Edit this at WikidataChemical and physical dataFormulaC26H22ClF3N2O3Molar mass502.92 g·mol−13D model (JSmol)
  • Interactive image
  • CC(C)C(Nc1ccc(C(F)(F)F)cc1Cl)C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1
InChI
  • InChI=1S/C26H22ClF3N2O3/c1-16(2)24(32-22-12-11-18(14-21(22)27)26(28,29)30)25(33)35-23(15-31)17-7-6-10-20(13-17)34-19-8-4-3-5-9-19/h3-14,16,23-24,32H,1-2H3 ☒N
  • Key:INISTDXBRIBGOC-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Fluvalinate[1] is a synthetic pyrethroid chemical compound contained as an active agent in the products Apistan,[2] Klartan, and Minadox, that is an acaricide (specifically, a miticide), commonly used to control Varroa mites in honey bee colonies,[citation needed] infestations that constitute a significant disease of such insects.

Fluvalinate is a stable, nonvolatile,[3] viscous, heavy oil (technical) soluble in organic solvents.[4] Although the compound may be found in drones, a study has found honey samples virtually absent of fluvalinate, on account of its affinity to beeswax.[5][better source needed]

Stereoisomerism

Fluvalinate is synthesized from racemic valine [(RS)-valine], the synthesis is not diastereoselective. Thus, fluvalinate is a mixture of four stereoisomers, each about 25%.[6]

Fluvalinate stereoisomers
(R,R)-Fluvalinat
(R,R)-configuration 		(S,S)-Fluvalinat
(S,S)-configuration
(S,R)-Fluvalinat
(S,R)-configuration 		(R,S)-Fluvalinat
(R,S)-configuration

Tau-fluvalinate (τ-fluvalinate) is the trivial name for (2R)-fluvalinate. The C atom in the valinate structure is in (R)-absolute configuration, while the second chiral atom is a mixture of (R)- and (S)-configurations:[4]

τ-Fluvalinate diastereomers
(R,R)-Fluvalinat
(R,R)-configuration 		(R,S)-Fluvalinat
(R,S)-configuration

See also

References

  1. ^ "Fluvalinate - an overview | ScienceDirect Topics". www.sciencedirect.com. Retrieved 2023-11-03.
  2. ^ "Apistan: Varroa Control". Vita Bee Health. 2023-06-28. Retrieved 2023-11-03.
  3. ^ "tau-fluvalinate", Pesticide Properties DataBase, University of Hertfordshire, retrieved June 24, 2017
  4. ^ a b "Tau-fluvalinate", PubChem. The Open Chemistry Database, National Institutes of Health, retrieved June 24, 2017
  5. ^ MAF Biosecurity New Zealand (2001), A Review of Treatment Options for Control of Varroa Mite in New Zealand [HortResearch Client Report No. 2001/249] (PDF), archived from the original (PDF) on 2016-09-11, retrieved 28 August 2016, This report was commissioned by MAF to aid in internal decision making only. This report in no way constitutes MAF's advice to beekeepers and is useful only as background information.
  6. ^ Whitacre DM (2012). Reviews of environmental contamination and toxicology. Springer. p. 125. ISBN 978-1-4614-3280-7.

Further reading

  • Bessin R (2016). "Varroa Mites Infesting Honey Bee Colonies [Insect & Pest Info, Home & Health Pests, ENTFACT-608, April 2016 revision]". North Lexington, KY: University of Kentucky, Department of Entomology. Retrieved 28 August 2016. Apistan is a product available that will kill the mites and cause the mites to drop from the bees. … Apistan strips, which contain the miticide fluvalinate, are available from most large beekeeping suppliers and can be used both for detection and treatment of varroa infestations.

External links

  • EPA: Tau-fluvalinate; Reregistration Eligibility Decision for Low Risk Pesticide; Notice of Availability
  • Tau-fluvalinate in the Pesticide Properties DataBase (PPDB)
  • Fluvalinate in the Pesticide Properties DataBase (PPDB)
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CarbamatesInorganic compoundsInsect growth regulatorsNeonicotinoidsOrganochloridesOrganophosphorusPyrethroidsRyanoidsOther chemicalsMetabolitesBiopesticides