A pyrethroid ester insecticide and acaricide
Technical Support & Resources

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

Fenvalerate

Item No. 29399

Technical Information
Formal Name
4-chloro-α-(1-methylethyl)-benzeneacetic acid, cyano(3-phenoxyphenyl)methyl ester
CAS Number
51630-58-1
Molecular Formula
C25H22ClNO3
Formula Weight
Purity
≥95%
Formulation
A neat oil
DMF: 30 mg/mlDMSO: 1 mg/mlEthanol: 5 mg/ml
SMILES
O=C(C(C1=CC=C(Cl)C=C1)C(C)C)OC(C#N)C2=CC=CC(OC3=CC=CC=C3)=C2
InChi Code
InChI=1S/C25H22ClNO3/c1-17(2)24(18-11-13-20(26)14-12-18)25(28)30-23(16-27)19-7-6-10-22(15-19)29-21-8-4-3-5-9-21/h3-15,17,23-24H,1-2H3
InChi Key
NYPJDWWKZLNGGM-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Recommended Products

Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    Add

    Add

    Add

    Add

    Cayman Chemical
    Visit Our Environmental Toxicology Resource Center

    Explore additional resources to study natural toxins, pollutants including PFAS and 6-PPD-Q, and their biological effects.

    ENVIRONMENTAL TOXICOLOGY TOOLS & SERVICES
    Product Description

    Fenvalerate is a pyrethroid ester insecticide and acaricide.1,2 It is a slow activator of voltage-gated sodium channel 1.8 (Nav1.8).1 It induces mortality in pyrethroid-susceptible and -resistant strains of M. domestica (LD50s = 0.014-5 µg/fly).3 Fenvalerate also induces mortality in tobacco budworm larvae but is associated with pyrethroid resistance with an increase in LD50 values from 1.01 to 20.85 µg/g over a six-year timeframe.4 It induces mortality in 95.5% of T. macfarlanei spider mites when applied to leaves at a concentration of 0.015%.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Choi, J.S., and Soderlund, D.M. Structure-activity relationships for the action of 11 pyrethroid insecticides on rat Nav1.8 sodium channels expressed in Xenopus oocytes. Toxicol. Appl. Pharmacol. 211(3), 233-244 (2006).

    2. Jose, V.T., and Shah, A.H. Chemical control of the spider mite, Tetranychus macfarlanei B & P, the pest of cotton. Pesticides 20(12), 19-23 (1986).

    3. Pedersen, L.-E.K. The potency of cyclopropane pyrethroid ethers against susceptible and resistant strains of the house fly Musca domestica. Experientia 42(9), 1057-1058 (1986).

    4. Martinez-Carrillo, J.L., and Reynolds, H.T. Dosage-mortality studies with pyrethroids and other insecticides on the tobacco budworm (Lepidoptera: Noctuidae) from the Imperial Valley, California. J. Econ. Entomol. 76(5), 983-986 (1983).