Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Chemical pesticides >  Insecticides >  Organochlorine pesticides >  Lufenuron

Lufenuron

Basic information Safety Supplier Related

Lufenuron Basic information

Product Name:
Lufenuron
Synonyms:
  • fluphenacur
  • (rs)-1-[2,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxyl)phenyl]3-(2,6-difluorobenzoyl)urea
  • cga-184,699
  • LUFENURON
  • Benzamide, N-2,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenylaminocarbonyl-2,6-difluoro-
  • lufenuron (bsi,iso,inn)
  • (RS)-1-[2,5-Dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]-3-(2,6-difluorobenzoyl)urea
  • N-[2,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)-phenyl-aminocarbonyl]-2,6-difluorobenzamide
CAS:
103055-07-8
MF:
C17H8Cl2F8N2O3
MW:
511.15
EINECS:
410-690-9
Product Categories:
  • PROGRAM
  • 103055-07-8
Mol File:
103055-07-8.mol
More
Less

Lufenuron Chemical Properties

Melting point:
174.1°
Density 
1.631±0.06 g/cm3(Predicted)
vapor pressure 
<0.4 x10 -3 Pa (25 °C)
Flash point:
170 °C
storage temp. 
0-6°C
solubility 
100mg/L in organic solvents at 20 ℃
form 
Solid
Water Solubility 
<0.06 mg l-1(25 °C)
pka
8.49±0.46(Predicted)
color 
Off-white to light yellow
JECFA Number
85
BRN 
8398291
InChIKey
PWPJGUXAGUPAHP-UHFFFAOYSA-N
LogP
5.12 at 25℃
CAS DataBase Reference
103055-07-8(CAS DataBase Reference)
EPA Substance Registry System
Benzamide, N-[[[2,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]amino]carbonyl]-2,6-difluoro- (103055-07-8)
More
Less

Safety Information

Hazard Codes 
Xi;N,N,Xi
Risk Statements 
43-50/53
Safety Statements 
2-24-37-60-61
RIDADR 
3077
WGK Germany 
2
HazardClass 
9
PackingGroup 
III
HS Code 
29242990
Toxicity
LD50 in rats (mg/kg): >2000 orally; LC50 in rats (mg/m3): >2350 (Buholzer)
More
Less

Lufenuron Usage And Synthesis

Description

Lufenuron is an insect development inhibitor of the benzoylphenyl urea class. It demonstrates activity against fleas that have fed on treated cats and dogs and become exposed to lufenuron in the host’s blood. Lufenuron also has activity by virtue of its presence in adult flea feces, leading to its ingestion by flea larvae. Both activities result in the production of eggs that are unable to hatch, causing significant reductions in flea larvae populations. The lipophilicity of lufenuron leads to its deposition in adipose tissues of animals from where it is slowly released into the bloodstream. This permits effective blood concentrations to be maintained throughout the recommended oral dosing interval of 1 month.

Uses

Lufenuron is used for the control of Lepidoptera and Coleoptera larvae on cotton, maize and vegetables, and of citrus whitefly and rust mites on citrus fruit. It is also used to control fleas on pets and cockroaches in houses.

Definition

ChEBI: Lufenuron is a benzoylurea insecticide, a dichlorobenzene, a N-acylurea, an aromatic ether and an organofluorine compound.

Flammability and Explosibility

Not classified

Pharmacology

Antiparasitic. Lufenuron is a benzoylurea insecticide. This class of insecticides was previously used on fruits to decrease damage by insects. Lufenuron (Program) has been used for prevention of flea infections in dogs and cats because it inhibits chitin synthesis. For this use, it has been given to dogs at a dose of 10 mg/kg every 30 days and to cats at a dose of 30 mg/kg every 30 days. It may also have some inhibition on fungal cell membranes because it inhibits the cell wall of fungi, which contain chitin, and other complex polysaccharides. Because of this property on fungal cell membranes, there has been interest in using lufenuron to treat dermatophytes in small animals. However, proven efficacy has been controversial. Well-controlled studies have not confirmed consistent efficacy for treating dermatophytes in animals.

Veterinary Drugs and Treatments

Lufenuron is approved for use in dogs and cats 6 weeks of age and older for the control of flea populations. The combination product of lufenuron and milbemycin (Sentinel?) is indicated for use in puppies and dogs 4 weeks and older for prevention and control flea populations, prevention of heartworm disease, control of adult hookworms, and the removal and control of adult roundworms and whipworms.
Lufeneron showed initial promise as a treatment for fungal infections, but the early enthusiasm has dampened considerably as efficacy appears doubtful.

Metabolic pathway

Only limited information is available in the open literature on the metabolism of lufenuron.

Degradation

Lufenuron is less stable at alkaline pH than under acidic conditions. The DT50 at 25 °C is 160 days at pH 5,70 days at pH 7 and 32 days at pH 9 (PM).

Mode of action

Lufenuron has no systemic or translaminar effect. It is persistent with a transovarial effect. It may reduce the egg-Iaying rate or hinder the hatching process of embryos.

LufenuronSupplier

Bailing Agrochemical Co., Ltd. Gold
Tel
0510-86822183
Email
info@bailingcn.com
Shanghai Yuzhicheng Pharmaceutical Technology Co., Ltd. Gold
Tel
18001856580
Email
2415195517@qq.com
Shanghai Boyle Chemical Co., Ltd.
Tel
021-50182298 021-50180596
Email
sales@boylechem.com
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Email
jkinfo@jkchemical.com
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com