الصفحة الرئيسية>>Signaling Pathways>> Membrane Transporter/Ion Channel>> Sodium Channel>>Bifenthrin

Bifenthrin (Synonyms: (±)-Bifenthrin)

رقم الكتالوجGC60642 Copy One-Click Copy Product Info

Bifenthrin هو مبيد حشري بيرثرويد صناعي يطيل فتح قنوات الصوديوم مما يؤدي إلى إزالة الاستقطاب الغشائي وإعاقة التوصيل في الجهاز العصبي للحشرات

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Bifenthrin التركيب الكيميائي

Cas No.: 82657-04-3

الحجم السعر المخزون الكميّة
10mM (in 1mL DMSO)
50٫00
متوفر
5mg
32٫00
متوفر
10mg
45٫00
متوفر
25mg
63٫00
متوفر
50mg
81٫00
متوفر
100mg
104٫00
متوفر

Tel:(909) 407-4943 Email: sales@glpbio.com


مراجعات العميل

بناء على آراء العملاء.

Sample solution is provided at 25 µL, 10mM.



Description of Bifenthrin

Bifenthrin is a pyrethroid insecticide whose principal target of the neurotoxic action is the neuronal membrane’s voltage-gated Na+ channel [1]. Bifenthrin has greater photostability and insecticidal activity, but is neurotoxic to various animals, and its clinical signs of toxicity including tremors and convulsions. [1, 2].

Bifenthrin (20μM; 24h) induced a marked increase in PGE2, NO and TNF-alpha production in primary microglia; Bifenthrin (20μM; 24h) increased the expression of IL-6 and TNF-alpha mRNA in primary microglia [3]. Bifenthrin (1, 1.5μM; 24h) significantly decreased glutathione peroxidase activity in erythrocytes; Bifenthrin (1.5μM; 24h) induced hemolysis in erythrocytes [2].

Bifenthrin (30, 60ng/L; 14d) increased the number of congested blood vessels of juvenile rainbow trout [4]. Bifenthrin (8mg/kg; 7d; i.p.) induced local nuclear pyknosis and vacuolar degeneration of liver tissues in some BALB/c mouse specimens; Bifenthrin (2, 4, 8mg/kg; 7d; i.p.) resulted in a concentration-dependent increase in mitochondrial ROS generation of BALB/c mice [5]. Bifenthrin (0.6mg/kg; 6weeks; qod.; i.g.) significantly increased body weight of C57BL/6 mice; Bifenthrin (0.6mg/kg; 6weeks; qod.; i.g.) significantly downregulated the expression of HSL and ATGL while significantly upregulated the expression of LPL of C57BL/6 mice [6].

References:
[1] Moreira C V L, Ogbu J s, Monteiro K L C, et al. Bifenthrin under scrutiny: revisiting toxicological evidence amid regulatory gaps [J]. Journal of applied toxicology : JAT, 2026, 46(1): 61-77.
[2] Mukhtar F, Jilani K, Bibi I, et al. Stimulation of erythrocyte membrane blebbing by Bifenthrin induced oxidative stress [J]. Dose-response : a publication of International Hormesis Society, 2022, 20(1): 15593258221076710.
[3] Gargouri B, Yousif N M, Bouchard M, et al. Inflammatory and cytotoxic effects of bifenthrin in primary microglia and organotypic hippocampal slice cultures [J]. Journal of neuroinflammation, 2018, 15(1): 159.
[4] Magnuson J T, Caceres L, Sy N, et al. The use of non-targeted lipidomics and histopathology to characterize the neurotoxicity of Bifenthrin to juvenile rainbow trout (Oncorhynchus mykiss) [J]. Environmental science & technology, 2022, 56(16): 11482-11492.
[5] Zhang Y, Lu M, Zhou P, et al. Multilevel evaluations of potential liver injury of bifenthrin [J]. Pesticide biochemistry and physiology, 2015, 122: 29-37.
[6] Wei C, Wang X, Yao X, et al. Bifenthrin induces fat deposition by improving fatty acid uptake and inhibiting lipolysis in mice [J]. Journal of agricultural and food chemistry, 2019, 67(51): 14048-14055.

Protocol of Bifenthrin

Cell experiment [1]:

Cell lines

Primary microglia of Sprague Dawley rats

Preparation Method

Microglial cells were exposed to Bifenthrin (DMSO as a control) for 24h. Gene expression of TNF-alpha and IL-6 was analyzed by real-time quantitative PCR.

Reaction Conditions

20μM; 24h

Applications

Bifenthrin increased the expression of IL-6 and TNF-alpha mRNA in primary microglia.
Animal experiment [2]:

Animal models

BALB/c mice

Preparation Method

The animals were exposed daily to Bifenthrin via a 0.3 mL intraperitoneal injection of the appropriate concentration in corn oil. After a 7-day treatment period, the livers were collected for analysis.

Dosage form

2, 4, 8mg/kg; 7d; i.p.

Applications

Bifenthrin resulted in a concentration-dependent increase in mitochondrial ROS generation.

References:
[1] Gargouri B, Yousif N M, Bouchard M, et al. Inflammatory and cytotoxic effects of bifenthrin in primary microglia and organotypic hippocampal slice cultures [J]. Journal of neuroinflammation, 2018, 15(1): 159.
[2] Zhang Y, Lu M, Zhou P, et al. Multilevel evaluations of potential liver injury of bifenthrin [J]. Pesticide biochemistry and physiology, 2015, 122: 29-37.

Chemical Properties of Bifenthrin

Cas No. 82657-04-3 SDF
المرادفات (±)-Bifenthrin
Canonical SMILES O=C([C@H]1C(C)(C)[C@H]1/C=C(Cl)/C(F)(F)F)OCC2=C(C)C(C3=CC=CC=C3)=CC=C2
Formula C23H22ClF3O2 M.Wt 422.87
الذوبان DMSO: 100 mg/mL (236.48 mM) Storage 4°C, protect from light
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of Bifenthrin

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 2.3648 mL 11.824 mL 23.6479 mL
5 mM 473 μL 2.3648 mL 4.7296 mL
10 mM 236.5 μL 1.1824 mL 2.3648 mL
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In vivo Formulation Calculator (Clear solution) of Bifenthrin

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

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Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL saline, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
3. All of the above co-solvents are available for purchase on the GlpBio website.

Product Documents

Quality Control & SDS

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مراجعات

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Average Rating: 5 ★★★★★ (Based on Reviews and 15 reference(s) in Google Scholar.)

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