Category: 153719-23-4

Application of 153719-23-4, Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn’t involve a screen. 153719-23-4, C8H10ClN5O3S. A document type is Patent, introducing its new discovery.

The invention discloses an insecticidal and disease-preventing suspended seed coating agent which is mainly characterized in that effective active components are fludioxonil and an effective component B, wherein a weight ratio of fludioxonil to the effective component B is 1:60-60:1. The composition is prepared into the suspended seed coating agent. The suspended seed coating agent provided by the invention has the advantages of good film-forming performance, uniform coating, high suspension rate, good safety, low toxicity, and the like. The suspended seed coating agent can be widely applied in seed treatments of crops such as wheat, corn, paddy rice, peanut, cotton, and the like. The seed coating agent has a sustained-release effect, such that pesticide dose is reduced. The seed coating agent is safe to human and animals, has no phytotoxicity, and has good environmental compatibility.

The invention discloses an insecticidal and disease-preventing suspended seed coating agent which is mainly characterized in that effective active components are fludioxonil and an effective component B, wherein a weight ratio of fludioxonil to the effective component B is 1:60-60:1. The composition is prepared into the suspended seed coating agent. The suspended seed coating agent provided by the invention has the advantages of good film-forming performance, uniform coating, high suspension rate, good safety, low toxicity, and the like. The suspended seed coating agent can be widely applied in seed treatments of crops such as wheat, corn, paddy rice, peanut, cotton, and the like. The seed coating agent has a sustained-release effect, such that pesticide dose is reduced. The seed coating agent is safe to human and animals, has no phytotoxicity, and has good environmental compatibility.

If you are hungry for even more, make sure to check my other article about 153719-23-4. Application of 153719-23-4

Reference£º
Thiazole | C3H8832NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Article£¬once mentioned of 153719-23-4, Application In Synthesis of N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide

A sensitive biotinylated indirect competitive enzyme-linked immunosorbent assay (Bic-ELISA) was developed to detect acetamiprid pesticides in pollen, based on the heterogeneous coating antigen and biotinylated anti-acetamiprid monoclonal antibody. Under optimized experimental conditions, the detection limit for the Bic-ELISA was 0.17 ng/mL and the linear range was 0.25?25 ng/mL. The cross-reactivities could be regarded as negligible for the biotinylated antibodies with their analogues except for thiacloprid (1.66%). Analyte recoveries for extracts of spiked pollen (camellia pollen, lotus pollen, rape pollen) ranged from 81.1% to 108.0%, with intra-day relative standard deviations (RSDs) of 4.8% to 10.9%, and the average reproducibility was 85.4% to 110.9% with inter-assay and inter-assay RSDs of 6.1% to 11.7%. The results of Bic-ELISA methods for the Taobao?s website samples were largely consistent with HPLC-MS/MS. Therefore, the established Bic-ELISA methods would be conducive to the monitoring of acetamiprid in pollen.

A sensitive biotinylated indirect competitive enzyme-linked immunosorbent assay (Bic-ELISA) was developed to detect acetamiprid pesticides in pollen, based on the heterogeneous coating antigen and biotinylated anti-acetamiprid monoclonal antibody. Under optimized experimental conditions, the detection limit for the Bic-ELISA was 0.17 ng/mL and the linear range was 0.25?25 ng/mL. The cross-reactivities could be regarded as negligible for the biotinylated antibodies with their analogues except for thiacloprid (1.66%). Analyte recoveries for extracts of spiked pollen (camellia pollen, lotus pollen, rape pollen) ranged from 81.1% to 108.0%, with intra-day relative standard deviations (RSDs) of 4.8% to 10.9%, and the average reproducibility was 85.4% to 110.9% with inter-assay and inter-assay RSDs of 6.1% to 11.7%. The results of Bic-ELISA methods for the Taobao?s website samples were largely consistent with HPLC-MS/MS. Therefore, the established Bic-ELISA methods would be conducive to the monitoring of acetamiprid in pollen.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.Application In Synthesis of N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 153719-23-4, in my other articles.

Reference£º
Thiazole | C3H8956NS – PubChem,
Thiazole | chemical compound | Britannica

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Patent£¬once mentioned of 153719-23-4, Quality Control of: N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide

The present invention relates to N-acylimino compound of formula (I): (I) wherein X1 is O or S, in particular O; X2 is CN or NO2; m is an integer selected from 0, 1, 2, 3, 4, 5 and 6; Het is a 5- or 6- membered carbon-bound or nitrogen-bound heterocyclic or heteroaromatic ring, W1 is O, S or NRw1; W2-W3-W4 isa bivalent radical selected from -C(Rv2Rw2)-C(Rv3Rw3)-, -C(Rv4)=C(Rv5)- and – C(Rv2Rw2)-O-C(Rv3Rw3)-; R1, R2 may be hydrogen, halogen, etc. R3 may be hydrogen, halogen, CN, C1-C6-alkyl, etc. R4a, R4b if present, may be hydrogen, halogen, C1-C6-alkyl, etc. R5 may be hydrogen, halogen, C1-C6-alkyl, C1-C6-alkenyl, C1-C6-alkynyl, C3-C8- cycloalkyl, S(O)nNR9aR9b, NR9aR9b, C(=O)OR8, C(=O)NR9aR9b, C(=S)NR9aR9b, C(=O)R7a, C(=S)R7a, NR9a-C(=O)R7a, NR9a-C(=S)R7a, NR9a-S(O)nR8a, a moitey Q-phenyl, where the phenyl ring is optionally substituted with one or more, e.g. 1, 2, 3, 4 or 5 identical or different substituents R10, or a moiety Q-HetNo., or R3 and R5 together may also form with the carbon atom they are bound to, a 3-, 4-, 5- or 6- membered saturated partially unsaturated carbocycle or heterocycle, wherein Rw1, Rw2, Rw3, Rv2, Rv3, Rv5, R7a, R8, R8a, R9a, R9b, Q, HetNo. are as defomed in the claims. The invention also relates to the use of the N-acylimino heterocyclic compounds, their stereoisomers, their tautomers and their salts, for combating invertebrate pests. Furthermore the invention relates also to methods of combating invertebrate pests, which comprises applying such compounds.

The present invention relates to N-acylimino compound of formula (I): (I) wherein X1 is O or S, in particular O; X2 is CN or NO2; m is an integer selected from 0, 1, 2, 3, 4, 5 and 6; Het is a 5- or 6- membered carbon-bound or nitrogen-bound heterocyclic or heteroaromatic ring, W1 is O, S or NRw1; W2-W3-W4 isa bivalent radical selected from -C(Rv2Rw2)-C(Rv3Rw3)-, -C(Rv4)=C(Rv5)- and – C(Rv2Rw2)-O-C(Rv3Rw3)-; R1, R2 may be hydrogen, halogen, etc. R3 may be hydrogen, halogen, CN, C1-C6-alkyl, etc. R4a, R4b if present, may be hydrogen, halogen, C1-C6-alkyl, etc. R5 may be hydrogen, halogen, C1-C6-alkyl, C1-C6-alkenyl, C1-C6-alkynyl, C3-C8- cycloalkyl, S(O)nNR9aR9b, NR9aR9b, C(=O)OR8, C(=O)NR9aR9b, C(=S)NR9aR9b, C(=O)R7a, C(=S)R7a, NR9a-C(=O)R7a, NR9a-C(=S)R7a, NR9a-S(O)nR8a, a moitey Q-phenyl, where the phenyl ring is optionally substituted with one or more, e.g. 1, 2, 3, 4 or 5 identical or different substituents R10, or a moiety Q-HetNo., or R3 and R5 together may also form with the carbon atom they are bound to, a 3-, 4-, 5- or 6- membered saturated partially unsaturated carbocycle or heterocycle, wherein Rw1, Rw2, Rw3, Rv2, Rv3, Rv5, R7a, R8, R8a, R9a, R9b, Q, HetNo. are as defomed in the claims. The invention also relates to the use of the N-acylimino heterocyclic compounds, their stereoisomers, their tautomers and their salts, for combating invertebrate pests. Furthermore the invention relates also to methods of combating invertebrate pests, which comprises applying such compounds.

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 153719-23-4 is helpful to your research., Quality Control of: N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide

Reference£º
Thiazole | C3H8717NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Patent£¬once mentioned of 153719-23-4, Application In Synthesis of N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide

The present invention relates to a pesticide composition intended for protecting plants, crops or seeds against phyto-pathogenic fungi or damaging insects, and the corresponding methods of treatment using the said composition. More precisely, the subject of the present invention is a pesticide composition based on fosetyl-Al, propamocarb-HCl, an insecticide active substance and optionally a further fungicide active substance.

The present invention relates to a pesticide composition intended for protecting plants, crops or seeds against phyto-pathogenic fungi or damaging insects, and the corresponding methods of treatment using the said composition. More precisely, the subject of the present invention is a pesticide composition based on fosetyl-Al, propamocarb-HCl, an insecticide active substance and optionally a further fungicide active substance.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application In Synthesis of N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide. In my other articles, you can also check out more blogs about 153719-23-4

Reference£º
Thiazole | C3H8737NS – PubChem,
Thiazole | chemical compound | Britannica

Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn¡¯t involve a screen. 153719-23-4, C8H10ClN5O3S. A document type is Patent, introducing its new discovery., Recommanded Product: N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide

Methods to control certain invertebrates including insects in agricultural, urban, animal health, and industrial systems by directly or systemically applying to a locus where control is desired an effective amount of a compound of N-substituted sulfoximines.

Methods to control certain invertebrates including insects in agricultural, urban, animal health, and industrial systems by directly or systemically applying to a locus where control is desired an effective amount of a compound of N-substituted sulfoximines.

Interested yet? Keep reading other articles of 153719-23-4!, Recommanded Product: N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide

Reference£º
Thiazole | C3H8900NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Patent£¬once mentioned of 153719-23-4, Computed Properties of C8H10ClN5O3S

Pesticide concentrates are provided containing an emulsifier that is an EPA list 4 inert and is a polyglycerol fatty acid ester, a sorbitan fatty acid ester or a combination thereof, a pesticide and a solvent that is either a EPA list 3 inert of acetyl ester, EPA list 4 inert of a methyl fatty ester, an acetyltributyl citrate, white mineral oil or a combination thereof. The pesticide can be a water-insoluble synthetic pyrethroid, natural pyrethrum, channel blocking insecticide, acetylcholinesterase inhibitor, oxadiazine, organophosphate, neonicotinoid insecticide, thiamethoxam, imidacloprid, acetamiprid, thiacloprid, clothianidin, nitenpyran, insect growth regulator, juvenile hormone mimic, fermentation insecticide, plant oil insecticide, acaracide, miticide, fungicide, herbicide and combinations thereof. The pesticide concentrate is diluted with a hydrocarbon solvent, a white mineral oil or a combination thereof and mixed with water. A corrosion inhibitor is added to form a stable water-in-oil emulsion in conjunction with a propellant to make a ready-to-use aerosol for home, garden and public health pest control.

Pesticide concentrates are provided containing an emulsifier that is an EPA list 4 inert and is a polyglycerol fatty acid ester, a sorbitan fatty acid ester or a combination thereof, a pesticide and a solvent that is either a EPA list 3 inert of acetyl ester, EPA list 4 inert of a methyl fatty ester, an acetyltributyl citrate, white mineral oil or a combination thereof. The pesticide can be a water-insoluble synthetic pyrethroid, natural pyrethrum, channel blocking insecticide, acetylcholinesterase inhibitor, oxadiazine, organophosphate, neonicotinoid insecticide, thiamethoxam, imidacloprid, acetamiprid, thiacloprid, clothianidin, nitenpyran, insect growth regulator, juvenile hormone mimic, fermentation insecticide, plant oil insecticide, acaracide, miticide, fungicide, herbicide and combinations thereof. The pesticide concentrate is diluted with a hydrocarbon solvent, a white mineral oil or a combination thereof and mixed with water. A corrosion inhibitor is added to form a stable water-in-oil emulsion in conjunction with a propellant to make a ready-to-use aerosol for home, garden and public health pest control.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.Computed Properties of C8H10ClN5O3S, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 153719-23-4, in my other articles.

Reference£º
Thiazole | C3H8890NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Patent£¬once mentioned of 153719-23-4, 153719-23-4

Pesticide concentrates are provided containing an emulsifier that is an EPA list 4 inert and is a polyglycerol fatty acid ester, a sorbitan fatty acid ester or a combination thereof, a pesticide and a solvent that is either a EPA list 3 inert of acetyl ester, EPA list 4 inert of a methyl fatty ester, an acetyltributyl citrate, white mineral oil or a combination thereof. The pesticide can be a water-insoluble synthetic pyrethroid, natural pyrethrum, channel blocking insecticide, acetylcholinesterase inhibitor, oxadiazine, organophosphate, neonicotinoid insecticide, thiamethoxam, imidacloprid, acetamiprid, thiacloprid, clothianidin, nitenpyran, insect growth regulator, juvenile hormone mimic, fermentation insecticide, plant oil insecticide, acaracide, miticide, fungicide, herbicide and combinations thereof. The pesticide concentrate is diluted with a hydrocarbon solvent, a white mineral oil or a combination thereof and mixed with water. A corrosion inhibitor is added to form a stable water-in-oil emulsion in conjunction with a propellant to make a ready-to-use aerosol for home, garden and public health pest control.

Pesticide concentrates are provided containing an emulsifier that is an EPA list 4 inert and is a polyglycerol fatty acid ester, a sorbitan fatty acid ester or a combination thereof, a pesticide and a solvent that is either a EPA list 3 inert of acetyl ester, EPA list 4 inert of a methyl fatty ester, an acetyltributyl citrate, white mineral oil or a combination thereof. The pesticide can be a water-insoluble synthetic pyrethroid, natural pyrethrum, channel blocking insecticide, acetylcholinesterase inhibitor, oxadiazine, organophosphate, neonicotinoid insecticide, thiamethoxam, imidacloprid, acetamiprid, thiacloprid, clothianidin, nitenpyran, insect growth regulator, juvenile hormone mimic, fermentation insecticide, plant oil insecticide, acaracide, miticide, fungicide, herbicide and combinations thereof. The pesticide concentrate is diluted with a hydrocarbon solvent, a white mineral oil or a combination thereof and mixed with water. A corrosion inhibitor is added to form a stable water-in-oil emulsion in conjunction with a propellant to make a ready-to-use aerosol for home, garden and public health pest control.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.153719-23-4, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 153719-23-4, in my other articles.

Reference£º
Thiazole | C3H8890NS – PubChem,
Thiazole | chemical compound | Britannica

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Patent, authors is WALTHAM, Mark£¬once mentioned of 153719-23-4, 153719-23-4

This invention relates to a method of pest and fungal control and more particularly to a method for combating pests and disease of ornamental plants by controlled release of insecticides and fungicides, which method comprises applying to the growing medium in which said plants are grown, a granular composition obtainable by preparing one or more melts comprising: 1-60% by weight of an insecticidal, nematicidal or fungicidal active ingredient or a combination of such ingredients and 20-80% by weight of at least one thermoplastic polymer to a total of 100% by weight; extruding or co-extruding the melt or melts and granulating the extrudate.

This invention relates to a method of pest and fungal control and more particularly to a method for combating pests and disease of ornamental plants by controlled release of insecticides and fungicides, which method comprises applying to the growing medium in which said plants are grown, a granular composition obtainable by preparing one or more melts comprising: 1-60% by weight of an insecticidal, nematicidal or fungicidal active ingredient or a combination of such ingredients and 20-80% by weight of at least one thermoplastic polymer to a total of 100% by weight; extruding or co-extruding the melt or melts and granulating the extrudate.

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 153719-23-4 is helpful to your research., 153719-23-4

Reference£º
Thiazole | C3H8674NS – PubChem,
Thiazole | chemical compound | Britannica

153719-23-4, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Patent, authors is Zhang, Wei£¬once mentioned of 153719-23-4

The invention discloses an oxa-fluoroalkyl sulfanilamide and neonicotinoid-containing insecticidal composition. The composition contains oxa-fluoroalkyl sulfanilamide and active constituent B. The active constituent B is a neonicotinoid insecticide which is one selected from thiamethoxam, thiacloprid, clothianidin and dinotefuran. The weight ratio of oxa-fluoroalkyl sulfanilamide to the active constituent B is 1:80-80:1. The composition can control various insect pests, has obvious synergistic effects, broadens the insecticidal spectrum and has high activity against various insect pests. The composition reduces dosage of pesticides, reduces residual quantity of pesticides on crops, reduces environmental pollution, is safe for people and livestock, and has advantages of good environmental compatibility and difficult generation of resistance to pesticide of insect pests.

The invention discloses an oxa-fluoroalkyl sulfanilamide and neonicotinoid-containing insecticidal composition. The composition contains oxa-fluoroalkyl sulfanilamide and active constituent B. The active constituent B is a neonicotinoid insecticide which is one selected from thiamethoxam, thiacloprid, clothianidin and dinotefuran. The weight ratio of oxa-fluoroalkyl sulfanilamide to the active constituent B is 1:80-80:1. The composition can control various insect pests, has obvious synergistic effects, broadens the insecticidal spectrum and has high activity against various insect pests. The composition reduces dosage of pesticides, reduces residual quantity of pesticides on crops, reduces environmental pollution, is safe for people and livestock, and has advantages of good environmental compatibility and difficult generation of resistance to pesticide of insect pests.

The reactant in an enzyme-catalyzed reaction is called a substrate. 153719-23-4 Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 153719-23-4 is helpful to your research.

Reference£º
Thiazole | C3H8829NS – PubChem,
Thiazole | chemical compound | Britannica

153719-23-4, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Patent, authors is SLATER, Russell£¬once mentioned of 153719-23-4

The invention relates to a method of controlling aphids that are resistant to neonicotinoid insecticides, using the compound 4,5-dihydro-6-methyl-4-(3- pyridylmethyleneamino)-1,2,4-triazin-3(2H)-one in free form or in agrochemically acceptable salt form as well as the use of compositions comprising said compound to control neonicontinoid resistant insects. In particular the methods relate to controlling neonicotinoid resistant insects in the Aphididae family, that are resistant to one or more neonicotinoid insecticides. Methods of the invention find particular use in controlling neonicotinoid resistant insects in crops of useful plants. Furthermore, the invention extends to methods of controlling plant viruses spread by neonicotinoid resistant insects.

The invention relates to a method of controlling aphids that are resistant to neonicotinoid insecticides, using the compound 4,5-dihydro-6-methyl-4-(3- pyridylmethyleneamino)-1,2,4-triazin-3(2H)-one in free form or in agrochemically acceptable salt form as well as the use of compositions comprising said compound to control neonicontinoid resistant insects. In particular the methods relate to controlling neonicotinoid resistant insects in the Aphididae family, that are resistant to one or more neonicotinoid insecticides. Methods of the invention find particular use in controlling neonicotinoid resistant insects in crops of useful plants. Furthermore, the invention extends to methods of controlling plant viruses spread by neonicotinoid resistant insects.

Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about 153719-23-4 is helpful to your research., 153719-23-4

Reference£º
Thiazole | C3H8807NS – PubChem,
Thiazole | chemical compound | Britannica