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35029

Supelco

Triflumuron

PESTANAL®, analytical standard

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About This Item

Formula empirica (notazione di Hill):
C15H10ClF3N2O3
Numero CAS:
64628-44-0
Peso molecolare:
358.70
Beilstein:
2776684
Numero CE:
264-980-3
Numero MDL:
MFCD00072496
Codice UNSPSC:
41116107
ID PubChem:
329755112
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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)
XAIPTRIXGHTTNT-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

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.

Applicazioni

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

Note legali

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

Pittogrammi

Skull and crossbones
GHS06

Avvertenze

Danger

Indicazioni di pericolo

H330

Classi di pericolo

Acute Tox. 2 Inhalation

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
BCCM1210
BCCF3175
BCBS6972V
SZBB343XV
SZB7080XV

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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
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
Thiago Affonso Belinato et al.
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
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
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
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