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35029

Supelco

Triflumuron

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C15H10ClF3N2O3
Número de CAS:
64628-44-0
Peso molecular:
358.70
Beilstein/REAXYS Number:
2776684
EC Number:
264-980-3
MDL number:
MFCD00072496
UNSPSC Code:
41116107
PubChem Substance ID:
329755112
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

FC(F)(F)Oc1ccc(NC(=O)NC(=O)c2ccccc2Cl)cc1

InChI

1S/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)

InChI key

XAIPTRIXGHTTNT-UHFFFAOYSA-N

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General description

Triflumuron is a non-sysmetic insect growth regulator or insecticide, which can inhibit chitin synthesis. Its can act against moulting the larvae and also cause infertility of the eggs.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H330

Hazard Classifications

Acute Tox. 2 Inhalation

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
BCCM1210
BCCF3175
BCBS6972V
SZBB343XV
SZB7080XV

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Memorias do Instituto Oswaldo Cruz, 104(1), 43-47 (2009-03-11)
The control of Aedes aegypti is impaired due to the development of resistance to chemical insecticides. Insect Growth Regulators (IGR) exhibit distinct mechanisms of action and are considered potential vector control alternatives. Studies regarding the effects of sublethal IGR doses
Ralf Nauen et al.
Pest management science, 62(5), 379-382 (2006-03-24)
The mode of action of the 2,4-diphenyl-1,3-oxazoline acaricide/insecticide etoxazole has been argued to be moulting inhibition, but experimental results supporting this hypothesis are lacking. This study investigated the effect of etoxazole on chitin biosynthesis in the fall armyworm, Spodoptera frugiperda
K E Smith et al.
Medical and veterinary entomology, 12(4), 430-437 (1998-11-24)
Field trials were carried out in 1995 and 1996 on farms in the south-west of England to assess the extent to which odour-baited targets could be used to suppress populations of the ectoparasitic blowfly, Lucilia sericata, in sheep pastures. Targets
M Martínez Galera et al.
Talanta, 76(4), 815-823 (2008-07-29)
This study reports the first analytical application of luminol chemiluminescence reaction for the sensitive detection of two benzoylurea insecticides (diflubenzuron and triflumuron). Off-line experiments demonstrated that previously irradiated traces of these benzoylurea insecticides largely enhanced the chemiluminescence emission yielded from
Ademir Jesus Martins et al.
Pest management science, 64(6), 676-680 (2008-02-08)
In Brazil, dengue vector control is hampered by the resistance of Aedes aegypti L. populations to organophosphates (OPs). Insect growth regulators (IGRs) are a promising alternative, as their mechanisms of action are different from those of conventional insecticides. The authors
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