153719-23-4 Usage
Description
Thiamethoxam, an oxadiazane derivative, is a neonicotinoid insecticide characterized by its tetrahydro-N-nitro-4H-1,3,5-oxadiazin-4-imine structure with (2-chloro-1,3-thiazol-5-yl)methyl and methyl substituents. It exhibits properties of an antifeedant, a carcinogenic agent, an environmental contaminant, a xenobiotic, and a neonicotinoid insecticide. Thiamethoxam is classified as an oxadiazane, a member of 1,3-thiazoles, an organochlorine compound, and a 2-nitroguanidine derivative. It is derived from a 2-chlorothiazole and appears as an off-white to pale yellow solid.
Uses
Used in Agricultural Industry:
Thiamethoxam is used as a broad-spectrum insecticide for controlling a wide range of sucking and chewing insect pests. It is applied through foliar, soil, or seed treatments and is effective against various pests that feed on roots, leaves, and other plant tissues. Thiamethoxam is utilized in the production of most row and vegetable crops, such as corn, soybeans, snap beans, and potatoes.
Used in Livestock and Poultry Industry:
Thiamethoxam is also used to control insects in livestock pens and poultry houses, helping to maintain a healthy environment for animals and reduce the impact of insect-borne diseases.
Used in Turf and Landscape Management:
The insecticide is employed in sod farms, golf courses, lawns, household plants, and tree nurseries to protect plants from insect damage and ensure their healthy growth.
Environmental Concerns:
Reports have shown that exposure to neonicotinoid pesticides, such as Thiamethoxam, can cause honeybees to have problems returning home after foraging, and bumblebee colonies to grow poorly and produce fewer queens. This highlights the need for responsible use and ongoing research into the environmental impact of Thiamethoxam and other neonicotinoid insecticides.
Flammability and Explosibility
Flammable
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).
Check Digit Verification of cas no
The CAS Registry Mumber 153719-23-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,7,1 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 153719-23:
(8*1)+(7*5)+(6*3)+(5*7)+(4*1)+(3*9)+(2*2)+(1*3)=134
134 % 10 = 4
So 153719-23-4 is a valid CAS Registry Number.
InChI:InChI=1/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/b11-8+
153719-23-4Relevant articles and documents
Experimental and DFT studies on the vibrational, electronic spectra and NBO analysis of thiamethoxam
Zhang, Fang,Zhang, Yu,Ni, Haiwei,Ma, Kuirong,Li, Rongqing
, p. 162 - 171 (2014)
Vibrational and electronic spectral measurements were performed for 3-(2-chloro-1,3-thiazol-5-ylmethyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene(nitro) amine (thiamethoxam). Optimized geometrical structure and harmonic vibrational frequencies were calculated
Thiamethoxam production method and extractant
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Paragraph 0088-0089; 0098-0099, (2020/05/01)
The invention provides a thiamethoxam production method and an extractant, belongs to the technical field of pesticides, particularly provides an extractant taking ethylene glycol salicylate as a complexing agent, and also provides a composite extractant. The extractant comprises a complexing agent and a diluent, and the complexing agent comprises the ethylene glycol salicylate and P204, wherein the extraction ratio of ethylene glycol salicylate to P204 is 1:1.5 to 1:2. The ethylene glycol salicylate used as the complexing agent and -N- of thiamethoxam have strong ion association to generate an ion extract with the same structure, so that the distribution ratio is increased; and when the extractant and the P204 are used for composite extraction, hydrogen bond association of the strong electron withdrawing group nitro -NO2 of thiamethoxam and -OH of P204 can be promoted, and when the extraction ratio of ethylene glycol salicylate to the P204 extractant is 1:(1.5-2), the distribution ratio can be synergistically increased, and the extraction rate is increased.
PROCESS FOR THE PREPARATION OF THIAMETHOXAM
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Page/Page column 18, (2019/05/22)
There is disclosed the use of a solvent system comprising a C1 to C4 alcohol, a substituted benzene derivative bearing two or more C1 to C4 alkyl substituents, or a mixture thereof in the preparation of a crystalline form of 3-(2-chloro-1, 3-thiazol-5-yl methyl)-5-methyl-1, 3, 5-oxadiazinan-4-yledene (nitro) amine (thiamethoxam). Crystalline thiamethoxam prepared in this way exhibits a significantly improved stability, in particular a resistance to photolysis, compared with crystalline thiamethoxam prepared using other solvents.
