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Lufenuron is an insect development inhibitor belonging to the benzoylphenyl urea class. It is a dichlorobenzene, N-acylurea, aromatic ether, and organofluorine compound. Lufenuron demonstrates activity against fleas that have fed on treated animals, as well as through its presence in adult flea feces, leading to ingestion by flea larvae. This results in the production of eggs that are unable to hatch, causing significant reductions in flea larvae populations. Its lipophilicity allows for deposition in adipose tissues of animals, from where it is slowly released into the bloodstream, maintaining effective blood concentrations throughout the recommended oral dosing interval of 1 month.

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  • 103055-07-8 Structure
  • Basic information

    1. Product Name: Lufenuron
    2. 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;LUFENURON PESTANAL, 100 MG;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
    3. CAS NO:103055-07-8
    4. Molecular Formula: C17H8Cl2F8N2O3
    5. Molecular Weight: 511.15
    6. EINECS: 410-690-9
    7. Product Categories: PROGRAM
    8. Mol File: 103055-07-8.mol
  • Chemical Properties

    1. Melting Point: 174.1°
    2. Boiling Point: N/A
    3. Flash Point: 170 °C
    4. Appearance: COA
    5. Density: 1.631 g/cm3
    6. Vapor Pressure: <0.4 x10 -3 Pa (25 °C)
    7. Refractive Index: 1.522
    8. Storage Temp.: 0-6°C
    9. Solubility: 100mg/L in organic solvents at 20 ℃
    10. PKA: 8.49±0.46(Predicted)
    11. Water Solubility: <0.06 mg l-1(25 °C)
    12. BRN: 8398291
    13. CAS DataBase Reference: Lufenuron(CAS DataBase Reference)
    14. NIST Chemistry Reference: Lufenuron(103055-07-8)
    15. EPA Substance Registry System: Lufenuron(103055-07-8)
  • Safety Data

    1. Hazard Codes: Xi;N,N,Xi
    2. Statements: 43-50/53
    3. Safety Statements: 2-24-37-60-61
    4. RIDADR: 3077
    5. WGK Germany: 2
    6. RTECS:
    7. HazardClass: 9
    8. PackingGroup: III
    9. Hazardous Substances Data: 103055-07-8(Hazardous Substances Data)

103055-07-8 Usage

Uses

Used in Agricultural Industry:
Lufenuron is used as a pesticide for the control of Lepidoptera and Coleoptera larvae on crops such as cotton, maize, and vegetables. It is also effective against citrus whitefly and rust mites on citrus fruit.
Used in Veterinary Medicine:
Lufenuron is used as an antiparasitic agent for controlling fleas on pets, such as cats and dogs. It helps in reducing flea larvae populations by preventing the hatching of eggs.
Used in Household Pest Control:
Lufenuron is used as an insecticide for controlling cockroaches in houses, providing an effective solution for pest management.

Flammability and Explosibility

Notclassified

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.

Check Digit Verification of cas no

The CAS Registry Mumber 103055-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,0,5 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103055-07:
(8*1)+(7*0)+(6*3)+(5*0)+(4*5)+(3*5)+(2*0)+(1*7)=68
68 % 10 = 8
So 103055-07-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H8Cl2F8N2O3/c18-6-5-11(32-17(26,27)14(22)16(23,24)25)7(19)4-10(6)28-15(31)29-13(30)12-8(20)2-1-3-9(12)21/h1-5,14H,(H2,28,29,30,31)

103055-07-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Sigma-Aldrich

  • (Y0001284)  Lufenuron  European Pharmacopoeia (EP) Reference Standard

  • 103055-07-8

  • Y0001284

  • 1,880.19CNY

  • Detail
  • Sigma-Aldrich

  • (Y0001261)  Lufenuron for peak identification  European Pharmacopoeia (EP) Reference Standard

  • 103055-07-8

  • Y0001261

  • 1,880.19CNY

  • Detail
  • USP

  • (1370779)  Lufenuron  United States Pharmacopeia (USP) Reference Standard

  • 103055-07-8

  • 1370779-200MG

  • 4,787.64CNY

  • Detail

103055-07-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name lufenuron

1.2 Other means of identification

Product number -
Other names Lufenuron

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:103055-07-8 SDS

103055-07-8Upstream product

103055-07-8Downstream Products

103055-07-8Relevant articles and documents

Method for exterminating termites

-

, (2008/06/13)

A method for exterminating termites comprising using an entomopathogenic nematode together with an inset-growth regulator or a slow-acting insecticide, wherein insecticidal effects are reinforced compared with the cases using singly the entomopathogenic nematode and the insect-growth regulator or the slow-acting insecticide, respectively, and a bait station for exterminating termites that contains an entomopathogenic nematode with an insect-growth regulator or a slow-acting insecticide. According to the invention, emission of harmful chemicals to environment can be suppressed. The invention is nonpoisonous for human being and livestock, and is useful for indoor or outdoor extermination of termites.

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

-

, (2008/06/13)

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.

Method for the treatment of coccidioidomycosis in warm-blooded animals

-

, (2008/06/13)

This invention relates to the use of acyl urea compounds for the treatment or prophylaxis of Coccidioides immitis infections in warm-blooded animals. The invention has particular application in the treatment, prophylaxis or reduction of coccidioidomycosis.

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