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| Product | Description | |
|---|---|---|
| Dinotefuran | analytical standard. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. |  |
| Dinotefuran | Dinotefuran, a new neonicotinoid, has excellent insecticidal properties due to disruption of the insect's nervous system by inhibiting nicotinic acetylcholine receptors. Synonyms: 2-methyl-1-nitro-3- (oxolan-3-ylmethyl) guanidineDinotefuran165252-70-01-Methyl-2-nitro-3- ( (tetrahydrofuran-3-yl) methyl) guanidineAlbarinMikeblockMTI-446; MTI 446; MTI446Dinotefuran [ISO]1-Methyl-2-nitro-3-(tetrahydro-3-furylmethyl)guanidineCHEBI:39183HSDB 74651-m. Grades: 95%. CAS No. 165252-70-0. Molecular formula: C7H14N4O3. Mole weight: 202.21. |  |
| Dinotefuran | Dinotefuran is an insecticide of the neonicotinoid class developed by Mitsui Chemicals for control of insect pests such as aphids, whiteflies, thrips, leafhoppers, leafminers, sawflies, mole cricket, white grubs, lacebugs, billbugs, beetles, mealybugs, and cockroaches on leafy vegetables, in residential and commercial buildings, and for professional turf management. Its mechanism of action involves disruption of the insects nervous system by inhibiting nicotinic acetylcholine receptors. In order to avoid harming beneficial insects such as bees, it should not be applied during bloom. ; In July of 2013, the state of Oregon temporarily restricted the use of dinotefuran pending the results of an investigation into a large bee kill.Dinotefuran is also used in veterinary medicine as a flea and tick preventative for dogs and as a flea preventative for cats. It is used in combination with pyriproxifen or permethrin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N-methyl-N-nitro-N"-[(tetrahydro-3-furanyl)methyl]guanidine;2-methyl-1-nitro-3-(oxolan-3-ylmethyl)guanidine;1-Methyl-2-nitro-3-((tetrahydrofuran-3-yl)methyl)guanidine;(EZ)-(RS)-1-methyl-2-nitro-3-(tetrahydro-3-furylmethyl)guanidine;rac-(Ξ)-N-methyl-N"-nitro-N-[(3R)-oxolan-3-ylmethyl]guanidine. Product Category: Inhibitors. Appearance: White crystalline powder. CAS No. 165252-70-0. Molecular formula: C7H14N4O3. Mole weight: 20 |  |
| Dinotefuran | Dinotefuran is an insecticide of the neonicotinoid class, its mechanism of action involves disruption of the insect's nervous system by inhibiting nicotinic acetylcholine receptors. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MTI-446. CAS No. 165252-70-0. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 1 g. Product ID: HY-B0827. |  |
| 2-Chloro-1,3-thiazole-5-carboxylic Acid | 2-Chloro-5-thiazolecarboxylic Acid (C411465) was studied as one of the metabolites of thiamethoxam, clothianidin, and dinotefuran in mice. Group: Biochemicals. Grades: Highly Purified. CAS No. 101012-12-8. Pack Sizes: 1g, 5g. Molecular Formula: C4H2ClNO2S. US Biological Life Sciences. |  Worldwide |
| 2-Chloro-5-thiazolecarboxylic Acid-13C3,15N | 2-Chloro-5-thiazolecarboxylic Acid-13C3,15N is an isotopically labeled analog of 2-Chloro-5-thiazolecarboxylic Acid (C411465), which was studied as one of the metabolites of thiamethoxam, clothianidin, and dinotefuran in mice. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500μg, 1mg. Molecular Formula: C13C3H2Cl15NO2S, Molecular Weight: 167.55. US Biological Life Sciences. | Worldwide |
| Ethyl 2-Chlorothiazole-5-carboxylate | Ethyl 2-chlorothiazole-5-carboxylate is an intermediate in the synthesis of 2-Chloro-5-thiazolecarboxylic Acid. It is one of the metabolites of thiamethoxam, clothianidin, and dinotefuran in mice. Synonyms: Ethyl 2-Chloro-5-thiazolecarboxylate; 5-Thiazolecarboxylic acid, 2-chloro-, ethyl ester; 2-Chloro-5-thiazolecarboxylic acid ethyl ester; 2-Chloro-thiazole-5-carboxylic acid ethyl ester. Grades: ≥95%. CAS No. 81449-93-6. Molecular formula: C6H6ClNO2S. Mole weight: 191.64. | |
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