- Thiamethoxam
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- $19.00 / 1KG
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2026-01-30
- CAS:153719-23-4
- Min. Order: 100KG
- Purity: 99%
- Supply Ability: 100 mt
- Thiamethoxam
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- $77.00 / 500mg
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2026-01-19
- CAS:153719-23-4
- Min. Order:
- Purity: 99.86%
- Supply Ability: 10g
- Thiamethoxam
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- $0.00 / 1kg
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2025-12-02
- CAS:153719-23-4
- Min. Order: 1kg
- Purity: 95
- Supply Ability: 200000
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| | Thiamethoxam Basic information |
| | Thiamethoxam Chemical Properties |
| Melting point | 139.1° | | Boiling point | 485.8±55.0 °C(Predicted) | | density | 1.71±0.1 g/cm3(Predicted) | | vapor pressure | 6.6 x 10-9 Pa (25 °C) | | storage temp. | Inert atmosphere,2-8°C | | solubility | DMSO: 250 mg/mL (857.02 mM) | | Water Solubility | 4.1 x 103 mg l-1 (25 °C) | | pka | 0.99±0.10(Predicted) | | form | Solid | | color | Off-white to yellow | | BRN | 8491021 | | Major Application | agriculture
environmental | | InChI | InChI=1S/C8H10ClN5O3S/c1-12-4-17-5-13(8(12)11-14(15)16)3-6-2-10-7(9)18-6/h2H,3-5H2,1H3 | | InChIKey | NWWZPOKUUAIXIW-DHZHZOJOSA-N | | SMILES | O1CN(C)C(=N[N+]([O-])=O)N(CC2SC(Cl)=NC=2)C1 | | LogP | -0.13 at 25℃ | | EPA Substance Registry System | Thiamethoxam (153719-23-4) |
| Hazard Codes | Xn | | Risk Statements | 22-50/53 | | Safety Statements | 22-61-60 | | RIDADR | UN 3077 9 / PGIII | | WGK Germany | 2 | | HS Code | 29341000 | | Storage Class | 4.1B - Flammable solid hazardous materials | | Hazard Classifications | Acute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Flam. Sol. 1
Repr. 2 | | Hazardous Substances Data | 153719-23-4(Hazardous Substances Data) | | Toxicity | LD50 in rats (mg/kg): 1563 orally, >2000 dermally; LD50 in bobwhite quail, mallard duck (mg/kg): 1552, 576 orally. LC50 (96hr) in rainbow trout, bluegill (mg/l): >100, >114 (Senn). |
| | Thiamethoxam Usage And Synthesis |
| Chemical Properties | Off-White to Pale Yellow Solid | | Uses | Thiamethoxam is a broad spectrum insecticide active against a
wide spectrum of sucking and chewing insect pests after foliar, soil or
seed treatment. | | Definition | ChEBI: Thiamethoxam is an oxadiazane that is tetrahydro-N-nitro-4H-1,3,5-oxadiazin-4-imine bearing (2-chloro-1,3-thiazol-5-yl)methyl and methyl substituents at positions 3 and 5 respectively. It has a role as an antifeedant, a carcinogenic agent, an environmental contaminant, a xenobiotic and a neonicotinoid insectide. It is an oxadiazane, a member of 1,3-thiazoles, an organochlorine compound and a 2-nitroguanidine derivative. It derives from a 2-chlorothiazole. | | Application | Thiamethoxam is a neonicotinoid insecticide that is used widely in Wisconsin. Thiamethoxam is the active ingredient in a variety of products used in agriculture to kill sucking and chewing insects that feed on roots, leaves, and other plant tissues. Agricultural uses include soil and seed treatments as well as leaf spraying for most row and vegetable crops like corn, soybeans, snap beans, and potatoes. It is also used to control insects in livestock pens, poultry houses, sod farms, golf courses, lawns, household plants, and tree nurseries. It was first registered by the U.S. Environmental Protection Agency in 1999. Reports show that when exposed to neonicotinid pesticides honeybees have probelms returnign home after foraging and bumblebee colonies grow poorly and produce fewer queens. | | Flammability and Explosibility | Flammable | | Synthesis | In a 500 ml round bottom flask, 70 g of N,N-dimethylformamide (DMF) as solvent, 150 g of anhydrous potassium carbonate as base, and 80 g of 3-methyl-4-nitroimino-1,3,5-oxadiazine as one of the reactants were added sequentially. The mixture was stirred and warmed to 50°C. 110 g of 2-chloro-5-(chloromethyl)thiazole was added dropwise at a rate of 50 ml/hour in a 250 ml constant pressure dropping funnel, ensuring that the reaction temperature did not exceed 50°C. After the dropwise addition was completed, the reaction was maintained at 50°C for 16 hours. Upon completion of the reaction, the mixture was cooled to 10°C and filtered to obtain the solid product thiamethoxam. Thiamethoxam was analyzed by liquid chromatography with a purity of 98.4% and a yield of 98%.The recovery of N,N-dimethylformamide was 92%. | | Metabolic pathway | All the information on thiamethoxam is taken from a summary of the
proceedings of meeting published by the manufacturer. Full experimental
details are not given in the report and the identity of metabolites is not
disclosed (Novartis, 1997). | | Degradation | Thiamethoxam is hydrolytically stable at pH 5 (half-life about 200-300
days). The compound is more labile at pH 9 where the half-life is a few
days. It is rapidly photodegraded with a half-life of about 1 hour. In
aquatic systems, degradation occurs under alkaline conditions and the
insecticide is rapidly photodegraded but not readily biodegraded
(Novartis, 1997). | | Mode of action | Thiamethoxam interferes with nicotinic acetylcholine receptors in the insect’s nervous system, which are essential for proper functioning of the nerves. Within hours of contact or ingestion of thiamethoxam, insects stop feeding. Death usually occurs within 24 to 48 hours.
The activity of thiamethoxam, or any insecticide, at the target site is just one factor in its efficacy. When comparing insecticides, other variables – including how the compound interacts with the environment, the plant and the insect – also contribute to its insecticidal mode of action.
The Insecticide Resistance Action Committee (IRAC) has organized insecticides into 28 groups, plus sub-groups, based on their modes of action. Thiamethoxam is a Group 4A insecticide (neonicotinoids). | | References | [1] Patent: CN106188032, 2016, A. Location in patent: Paragraph 0017-0019
[2] Patent: CN103880832, 2016, B. Location in patent: Paragraph 0027-0029
[3] Patent: WO2015/180585, 2015, A1. Location in patent: Page/Page column 13-18
[4] Patent: CN107698578, 2018, A. Location in patent: Paragraph 0028; 0035; 0036; 0040-0042; 0049
[5] Patent: CN108164522, 2018, A. Location in patent: Paragraph 0027; 0030; 0034; 0038 |
| | Thiamethoxam Preparation Products And Raw materials |
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