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137 results about "Lufenuron" patented technology

Lufenuron is the active ingredient in the veterinary flea control medication program, and one of the two active ingredients in the flea, heartworm, ringworm and anthelmintic medicine milbemycin oxime/lufenuron (Sentinel).

Pesticidal composition

InactiveUS20080009452A1Effective knock-down actionEffective long-term actionBiocideDead animal preservationFipronilNovaluron
The present invention provides an insecticidal composition comprising of at least one insecticidal compound with effective knock-down action selected from among group (A) comprising of imidacloprid, acetamiprid, thiamethoxam, thiacloprid, nitenpyram, dinotefuran, clothianidin, abamectin, emamectin, emamectin benzoate and fipronil, and at least one insecticidal compound with effective long-term action selected from among group (B) of insect growth regulators comprising of benzoylphenyl urea (BPU) compounds selected from among novaluron, lufenuron, hexaflumuron, triflumuron, diflubenzuron, chlorfluazuron, flufenoxuron, noviflumuron and teflubenzuron. Optionally, said insecticidal composition may further contain excipients and/or additives and/or surface active agents. Further provided is a method for insect control, comprising of applying at least one insecticidal compound with effective knock-down action selected from among group (A) comprising of imidacloprid, acetamiprid, thiamethoxam, thiacloprid, nitenpyram, dinotefuran, clothianidin, abamectin, emamectin, emamectin benzoate and fipronil, and at least one insecticidal compound with effective long-term action selected from among group (B) of insect growth regulators (IGR) comprising of benzoylphenyl urea (BPU) compounds; to a crop, agricultural product, plant matter, animal or locale.
Owner:MAKHTESHIM CHEM WORKS

Synthesis method of benzamide pesticide lufenuron

The invention discloses a synthesis method of benzamide pesticide lufenuron, 2, 5-dichlorophenol is takend as a raw material, the lufenuron is obtained through the steps of addition with hexafluoropropylene, nitration, reduction and condensation in sequence, and the synthesis method is characterized in that the addition step of 2, 5-dichlorophenol and hexafluoropropylene comprises the following steps: adding 2, 5-dichlorophenol (SMN-SM-1), acetonitrile, phenol and a sodium carbonate aqueous solution into a reaction kettle, uniformly stirring and mixing, vacuumizing, controlling the temperature of cooling water to be 20-25 DEG C, introducing hexafluoropropylene, controlling the ventilation speed to ensure that the temperature in the reaction kettle is not higher than 25 DEG C and no positive pressure exists in the reaction kettle, and carrying out heat preservation reaction for 1-1.5 hours after ventilation is finished to obtain an intermediate SMN-Z1; the method is high in yield, good in product quality and easy to operate, solvents and catalysts used in the whole production process are all recycled and reused, the production cost is reduced, meanwhile, environmental protection is facilitated, and the method is more suitable for industrial production requirements.
Owner:CHONGQING MEDICAL & PHARMA COLLEGE
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