64628-44-0

Basic information

• Product Name: Triflumuron
• Synonyms: triflumuron (bsi,iso), alsystin;BAYSIR;Triflumuron,W.P.;Triflumuron suspension;1-（2-chlorobenzoyl)-3-(4-trifluoromethoxyphenyl) urea;OMS 2015;N-(2-Chlorobenzoyl)-N'-[4-(trifluoromethoxy)phenyl]urea;BAY-8514
• CAS NO: 64628-44-0
• Molecular Formula: C₁₅H₁₀ClF₃N₂O₃
• Molecular Weight: 358.7
• EINECS: 264-980-3
• Product Categories: INSECTICIDE;Alpha sort;Growth regulatorsPesticides&Metabolites;Insecticides;Pesticides;Q-ZAlphabetic;TP - TZ
• Mol File: 64628-44-0.mol
• Article Data: 9

Chemical Properties

• Melting Point: 198℃
• Appearance: /
• Density: 1.475 g/cm³
• Vapor Pressure: 0Pa at 20℃
• Refractive Index: 1.581
• Storage Temp.: 0-6°C
• Solubility: Soluble in DMF
• PKA: 9.79±0.46(Predicted)
• Water Solubility: 40μg/L at 20℃
• BRN: 2776684
• CAS DataBase Reference: Triflumuron(CAS DataBase Reference)
• NIST Chemistry Reference: Triflumuron(64628-44-0)
• EPA Substance Registry System: Triflumuron(64628-44-0)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 2
• RTECS: CV2474000
• Hazardous Substances Data: 64628-44-0(Hazardous Substances Data)

Usage

Description

Triflumuron, a benzoylphenyl urea compound, is an insect development inhibitor that inhibits the synthesis of chitin. It is formulated as an off-shears pour-on lousicide for control of the sheep body louse Bovicola ovis.

Chemical Properties

White Solid

Uses

Different sources of media describe the Uses of 64628-44-0 differently. You can refer to the following data:
1. Triflumuron is a benzoylphenylurea insecticide. Triflumuron is a chitin synthesis inhibitor used to control insects pests such as mosquitos and flies.
2. A chitin biosynthesis inhibitor
3. Insecticide (larvicide).

Flammability and Explosibility

Notclassified

Toxicity evaluation

Acute oral LD50 for rats: >5,000 mg/kg

InChI:InChI=1/C15H10ClF3N2O3/c16-12-4-2-1-3-11(12)13(22)21-14(23)20-9-5-7-10(8-6-9)24-15(17,18)19/h1-8H,(H2,20,21,22,23)

Upstream product

• 89-97-4 2-CHLOROBENZYLAMINE 
• 35037-73-1 1-isocyanato-4-trifluoromethoxy-benzene 
• 615-41-8 2-iodochlorobenzene 
• 82971-90-2 1-(4-(trifluoromethoxy)phenyl)urea 
• 82102-37-2 9-methyl-9H-fluorene-9-carbonyl chloride 

Relevant articles and documents

Hydrogen bond directed aerobic oxidation of amines via photoredox catalysis

An application of H-bonding interactions for directing the α-C-H oxidation of amines to amides and amino-ketones catalyzed by an organic photocatalyst is reported. The high efficiency of this method is demonstrated by the aerobic oxidation of pyrrolidines, diarylamines and benzylamines bearing urea groups with high yields and a wide substrate scope.

Active agent combinations

The novel active compound combinations of extracts from seeds of the neem tree and the active compounds of groups (B) to (F) listed in the description have very good insecticidal and acaricidal properties.

Insecticidal combination to control mammal fleas, in particular fleas on cats and dogs

Process and composition, in particular for controlling fleas on small mammals, characterized in that the composition includes, on the one hand, at least one insecticide of 1-N-arylpyrazole type, in particular fipronil, and, on the other hand, at least one compound of IGR (insect growth regulator) type, in doses and proportions which are parasiticidally effective on fleas, in a fluid vehicle which is acceptable for the animal and convenient for local application to the skin, preferably localized over a small surface area.