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46119

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Pymetrozin

PESTANAL®, analytical standard

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About This Item

Formula empirica (notazione di Hill):
C10H11N5O
Numero CAS:
123312-89-0
Peso molecolare:
217.23
Beilstein:
7814151
Numero MDL:
MFCD01632346
Codice UNSPSC:
41116107
ID PubChem:
329756612
NACRES:
NA.24

Grado

analytical standard

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

applicazioni

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

Stringa SMILE

CC1=NNC(=O)N(C1)\N=C\c2cccnc2

InChI

1S/C10H11N5O/c1-8-7-15(10(16)14-13-8)12-6-9-3-2-4-11-5-9/h2-6H,7H2,1H3,(H,14,16)/b12-6+
QHMTXANCGGJZRX-WUXMJOGZSA-N

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Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Note legali

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

Pittogrammi

Health hazardEnvironment
GHS08,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H351,H361fd,H410

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Repr. 2

Codice della classe di stoccaggio

13 - Non Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Ralf Nauen et al.
Pest management science, 69(4), 457-461 (2013-01-18)
Resistance to neonicotinoid insecticides such as imidacloprid in the cotton whitefly, Bemisia tabaci, is linked to its hydroxylation by constitutively overexpressed CYP6CM1, a cytochrome P450 enzyme. Here, an investigation was conducted to establish whether CYP6CM1 functionally expressed in Sf9 cells
Guoqing Shen et al.
Journal of hazardous materials, 164(2-3), 497-501 (2008-09-20)
The disappearance kinetics of pymetrozine was studied in a broccoli-field ecosystem, and an efficient method for the determination of pymetrozine in broccoli and soil was also developed. Pymetrozine residues were extracted from samples using acetonitrile. The extracts were cleaned up
Dhana Raj Boina et al.
Pest management science, 67(2), 146-155 (2010-10-21)
Vector-borne plant disease management can be enhanced by deployment of antifeedants in addition to the use of broad-spectrum neurotoxic insecticides. The effects of pymetrozine on Asian citrus psyllid (ACP), Diaphorina citri Kuwayama, feeding behaviour, survival and transmission of Candidatus Liberibacter
Kevin Gorman et al.
Pest management science, 66(11), 1186-1190 (2010-07-16)
Although cross-resistance between compounds in the same insecticide group is a frequently observed phenomenon, cross-resistance between groups that differ in structural and functional characteristics can be extremely unpredictable. In the case of controlling the whitefly, Bemisia tabaci Gennadius, neonicotinoids and
Lanfeng Ban et al.
Journal of economic entomology, 105(6), 2129-2135 (2013-01-30)
Laodelphax striatellus (Fallén) is a major pest of cultivated rice. Pymetrozine, a pyridine azomethine compound, represents a novel insecticide with a selective activity against sucking pests. The resistance of L. striatellus to thiamethoxam, nitenpyram, chlorpyrifos, and pymetrozine in five field
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