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D-Phenothrin

CAS No. 26046-85-5

D-Phenothrin ( (-)-trans-Phenothrin )

Catalog No. M26559 CAS No. 26046-85-5

D-Phenothrin is used in veterinary medicine to control pests on animals and to protect crops. D-Phenothrin is an orally effective type II synthetic pyrethroid widely used to kill insects, mosquitoes and human lice.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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5MG 46 Get Quote
10MG 65 Get Quote
25MG 119 Get Quote
50MG 168 Get Quote
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Biological Information

  • Product Name
    D-Phenothrin
  • Note
    Research use only, not for human use.
  • Brief Description
    D-Phenothrin is used in veterinary medicine to control pests on animals and to protect crops. D-Phenothrin is an orally effective type II synthetic pyrethroid widely used to kill insects, mosquitoes and human lice.
  • Description
    D-Phenothrin is used in veterinary medicine to control pests on animals and to protect crops. D-Phenothrin is an orally effective type II synthetic pyrethroid widely used to kill insects, mosquitoes and human lice.(In Vivo):D-Phenothrin administered to rats intraperitoneally for 14 consecutive days generated free radical species in a dose-dependent manner and caused oxidative DNA damage in the liver and kidney.
  • Synonyms
    (-)-trans-Phenothrin
  • Pathway
    Microbiology/Virology
  • Target
    Parasite
  • Recptor
    Akt; CB1; Human Endogenous Metabolite; PPARγ
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    26046-85-5
  • Formula Weight
    350.5
  • Molecular Formula
    C23H26O3
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CC(C)=C[C@@H]1[C@@H](C(=O)OCc2cccc(Oc3ccccc3)c2)C1(C)C
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Wang S, et al. N-Oleoyl glycine, a lipoamino acid, stimulates adipogenesis associated with activation of CB1 receptor and Akt signaling pathway in 3T3-L1 adipocyte. Biochem Biophys Res Commun. 2015 Oct 23;466(3):438-43.
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