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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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J L Lewis et al.
Environmental entomology, 39(1), 98-104 (2010-02-12)
Eastern subterranean termite, Reticulitermes flavipes (Kollar), workers were continuously exposed to one of five chitin synthesis inhibiting (CSI) active ingredients and the protist community from the hindgut quantified biweekly for 21 d. The CSIs tested included commercially available formulations of
Michael I Haverty et al.
Journal of economic entomology, 103(3), 770-780 (2010-06-24)
The objective of this study was to evaluate lufenuron termite bait (1,500 ppm) for the elimination of colonies of Reticulitermes hesperus Banks (Isoptera: Rhinotermitidae). Dispersion of colonies in six baited and six unbaited sites near Placerville, CA, was determined by
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
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
S Khay et al.
Bulletin of environmental contamination and toxicology, 81(4), 369-372 (2008-07-02)
Chinese cabbage has long been consumed as a staple food by the Koreans in various forms of fresh, salted, or fermented as kimchi. To fulfill the off-season demand for this crop, it has become a common practice to be cultivated
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