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Y0001284

Lufenuron

European Pharmacopoeia (EP) Reference Standard

Synonym(s):

1-[2,5-Dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]-3-(2,6-difluorobenzoyl)urea

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About This Item

Empirical Formula (Hill Notation):
C17H8Cl2F8N2O3
CAS Number:
103055-07-8
Molecular Weight:
511.15
Beilstein:
8398291
MDL number:
MFCD00867616
UNSPSC Code:
41116107
PubChem Substance ID:
329831341
NACRES:
NA.24

grade

pharmaceutical primary standard

API family

lufenuron

manufacturer/tradename

EDQM

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

SMILES string

FC(C(F)(F)F)C(F)(F)Oc1cc(Cl)c(NC(=O)NC(=O)c2c(F)cccc2F)cc1Cl

InChI

1S/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)

InChI key

PWPJGUXAGUPAHP-UHFFFAOYSA-N

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General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the Issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Lufenuron EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Packaging

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Other Notes

Sales restrictions may apply.

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H317,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

>338.0 °F - (External MSDS)

Flash Point(C)

> 170 °C - (External MSDS)

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Martín Breijo et al.
Veterinary parasitology, 181(2-4), 341-344 (2011-05-20)
The aim of this work was to evaluate the potential of lufenuron, a benzylphenylurea with ability to interfere with the formation of insect exoskeleton, as a therapeutic drug for larval echinococcosis (hydatid disease). For this purpose lufenuron, alone or in
Vicente Navarro-Llopis et al.
Pest management science, 66(5), 511-519 (2010-01-27)
The chemosterilisation technique has been demonstrated to reduce the population and fruit damage of the Mediterranean fruit fly, Ceratitis capitata (Wiedemann), in citrus orchards. Field trials showed efficacy by reducing the fruit fly population, which was progressively achieved by continuous
Umesh Gangishetti et al.
European journal of cell biology, 88(3), 167-180 (2008-11-11)
Chitin is an essential constituent of the insect exoskeleton, the cuticle, which is an extracellular matrix (ECM) covering the animal. It is produced by the glycosyltransferase chitin synthase at the apical plasma membrane of epidermal and tracheal cells. To fulfil
Theo C M Brock et al.
Environmental toxicology and chemistry, 29(9), 1994-2008 (2010-09-08)
Under typical agricultural use of an insecticide, it is likely that only part of an edge-of-field drainage ditch will be directly contaminated by spray drift. The response, including recovery, of aquatic macroinvertebrates in sprayed ditch sections may be affected by
Francesca Mancianti et al.
Journal of feline medicine and surgery, 11(2), 91-95 (2008-08-08)
The effectiveness of enilconazole (4 weekly rinses with a 0.2% solution) or griseofulvin (50mg/kg twice daily for 40 days) following a pre-treatment with oral lufenuron (100mg/kg by-weekly for 8 weeks) was tested on 25 (11+14) Microsporum canis infected cats. Control
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