Items 41 to 50 of 125 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Oxfendazole | 53716-50-0 | sc-205782 sc-205782A | 10 g 25 g | $166.00 $302.00 | ||
Oxfendazole functions as an insecticidal reagent by disrupting the energy metabolism of target insects. It interferes with mitochondrial function, inhibiting ATP synthesis and leading to energy depletion. This disruption triggers a cascade of metabolic failures, ultimately resulting in insect mortality. Its unique ability to penetrate the insect exoskeleton, combined with its selective toxicity, enhances its efficacy while reducing harm to beneficial species. | ||||||
Praziquantel | 55268-74-1 | sc-204857 | 5 g | $82.00 | 1 | |
Praziquantel acts as an insecticidal reagent by targeting the neuromuscular system of insects. It enhances calcium ion influx through specific channels, leading to paralysis and eventual death. This compound exhibits a high affinity for binding to certain receptors, disrupting synaptic transmission and causing hyperactivity in the nervous system. Its lipophilic nature allows for effective penetration of insect cuticles, ensuring rapid action against pests while minimizing impact on non-target organisms. | ||||||
(±)-Nicotine-d3 salicylate salt | 65636-94-4 | sc-301470 | 5 mg | $306.00 | ||
(±)-Nicotine-d3 salicylate salt functions as an insecticidal reagent by modulating neurotransmitter release at synaptic junctions, particularly affecting acetylcholine pathways. Its unique isotopic labeling enhances tracking in biological systems, allowing for detailed studies of its metabolic pathways. The compound's ability to disrupt ion channel dynamics leads to increased excitability and eventual insect mortality. Additionally, its solubility profile facilitates effective absorption through insect exoskeletons, promoting swift action against targeted pests. | ||||||
Dihydroavermectin B1a | 70161-11-4 | sc-202138 | 5 mg | $327.00 | 1 | |
Dihydroavermectin B1a acts as an insecticidal reagent by binding to glutamate-gated chloride channels, leading to hyperpolarization of nerve and muscle cells in insects. This unique interaction disrupts neuromuscular transmission, resulting in paralysis and death. Its high lipophilicity enhances penetration through the insect cuticle, ensuring rapid efficacy. The compound's stability under various environmental conditions further contributes to its effectiveness in pest management strategies. | ||||||
Dihydroavermectin B1b | 70209-81-3 | sc-202139 sc-202139-CW | 500 µg 500 µg | $301.00 $455.00 | 1 | |
Dihydroavermectin B1b functions as an insecticidal reagent by selectively targeting gamma-aminobutyric acid (GABA) receptors in insects, which disrupts inhibitory neurotransmission. This interaction leads to uncontrolled neural activity, causing paralysis. Its unique structural features enhance binding affinity, while its moderate solubility facilitates absorption through insect exoskeletons. Additionally, the compound exhibits prolonged residual activity, making it effective in various pest control applications. | ||||||
Milbemycin D | 77855-81-3 | sc-202228 sc-202228-CW sc-202228A | 1 mg 1 mg 5 mg | $395.00 $793.00 $1375.00 | 2 | |
Milbemycin D acts as an insecticidal reagent by interfering with glutamate-gated chloride channels in the nervous systems of target insects. This disruption results in hyperpolarization of neurons, leading to paralysis and eventual death. Its unique molecular structure allows for high specificity and potency, while its lipophilic nature enhances penetration through insect cuticles. The compound's stability under environmental conditions contributes to its effectiveness in pest management strategies. | ||||||
Nemadectin | 102130-84-7 | sc-202239 sc-202239A | 1 mg 5 mg | $357.00 $1428.00 | ||
Nemadectin functions as an insecticidal reagent by targeting specific ion channels, particularly those associated with gamma-aminobutyric acid (GABA) receptors in insects. This interaction disrupts neurotransmission, causing an accumulation of inhibitory signals that lead to paralysis. Its unique stereochemistry enhances binding affinity, while its hydrophobic characteristics facilitate absorption through insect exoskeletons. Additionally, Nemadectin exhibits remarkable stability, ensuring prolonged efficacy in various environmental conditions. | ||||||
Eprinomectin | 123997-26-2 | sc-204740 sc-204740B | 100 mg 500 mg | $151.00 $315.00 | ||
Eprinomectin acts as an insecticidal reagent by selectively binding to glutamate-gated chloride channels in the nervous systems of target insects. This binding disrupts ion flow, resulting in hyperpolarization and subsequent paralysis. Its lipophilic nature allows for effective penetration of the insect cuticle, enhancing bioavailability. Furthermore, Eprinomectin's unique structural features contribute to its low toxicity in non-target organisms, making it a safer option in integrated pest management strategies. | ||||||
Emamectin B1 Benzoate | 137512-74-4 | sc-204737 sc-204737A | 100 mg 250 mg | $48.00 $80.00 | 1 | |
Emamectin B1 Benzoate functions as an insecticidal reagent by targeting gamma-aminobutyric acid (GABA) receptors in the nervous systems of insects. This interaction leads to prolonged opening of chloride channels, causing an influx of ions that results in paralysis. Its high affinity for lipid membranes facilitates rapid absorption, while its stability under various environmental conditions enhances its efficacy. Additionally, its selective action minimizes impact on beneficial species, promoting ecological balance. | ||||||
Cycloechinulin | 143086-29-7 | sc-202114 | 1 mg | $205.00 | ||
Cycloechinulin acts as an insecticidal reagent by disrupting the energy metabolism of target insects. It interferes with mitochondrial function, leading to impaired ATP production and increased oxidative stress. This compound exhibits unique binding properties to specific enzyme sites, inhibiting critical metabolic pathways. Its lipophilic nature allows for effective penetration of insect cuticles, enhancing bioavailability. Furthermore, its rapid degradation in non-target environments reduces ecological risks. | ||||||