Bifenthrin

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Bifenthrin

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Cat No: 24057

Biochemicals - Pesticides

Bifenthrin is a synthetic pyrethroid insecticide that prolongs opening of sodium channels resulting in membrane depolarization and conductance block in the insect nervous system.{36375} It is effective against A. gambiae and C. quinquefasciatus mosqui...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

(1R,3R)-rel-3-[(1Z)-2-chloro-3,3,3-trifluoro-1-propen-1-yl]-2,2-dimethyl-cyclopropanecarboxylic acid, (2-methyl[1,1'-biphenyl]-3-yl)methyl ester

Correlated keywords:

92880-79-0 107497-60-9 107538-32-9 AGST 02002 AGST02002 Allectus Bifen XTS BifenXTS Bifenthrine Bifenture Biflex FT Biphenate Biphenthrin Biphentrin Bixan Bixan MG Brigade 10WP Brigata Flo Capture 2EC LFR pesticide DeterMite Discipline Empower FMC 54800 Fanfare Gyro Kiros EV Maxxthor OMS3024 OMS-3024 Onyx Seizer Semafor Silencer Sniper pyrethroid Talstar EZ F Pro One TalstarEZ TalstarPro TalstarOne Torant Transport Zipak Anopheles Culex Orius Daphnia

Product Overview:
Bifenthrin is a synthetic pyrethroid insecticide that prolongs opening of sodium channels resulting in membrane depolarization and conductance block in the insect nervous system.{36375} It is effective against A. gambiae and C. quinquefasciatus mosquitos (LD50s = 0.15 and 0.16 ng/mg, respectively) and increases O. insidiosus mortality in treated corn and sorghum plants.{41760,41761} Bifenthrin exhibits aquatic toxicity, inducing reproductive defects and lethality in D. magna (LC50 = 12.4 µg/L).{41762} Acute oral administration of bifenthrin induces fine tremor, decreases motor activity and grip strength, and increases pawing and head shaking behaviors in rats, indicating typical Type I pyrethroid neurotoxicity.{41763} Bifenthrin (8 mg/kg) also decreases locomotor activity, induces anemia, elevates white blood cell counts, alanine transaminase (ALT), and superoxide dismutase (SOD), as well as decreases glutathione peroxidase (Gpx) activity in mice.{41764}

Size	5 mg
Shipping	dry ice
CAS Number	82657-04-3
Molecular Formula	C₂₃H₂₂ClF₃O₂
SMILES	CC1=C(C2=CC=CC=C2)C=CC=C1COC([C@H]3C(C)(C)[C@H]3/C=C(Cl)/C(F)(F)F)=O
Molecular Weight	422,9
Formulation	A solid
Purity	≥98%
Custom Code	2914.50
UNSPSC code	12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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