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46119

Supelco

Pymetrozin

PESTANAL®, analytical standard

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About This Item

Empirische Formel (Hill-System):
C10H11N5O
CAS-Nummer:
123312-89-0
Molekulargewicht:
217.23
Beilstein:
7814151
MDL-Nummer:
MFCD01632346
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329756612
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Anwendung(en)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

Format

neat

SMILES String

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+

InChIKey

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.

Rechtliche Hinweise

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

Piktogramme

Health hazardEnvironment
GHS08,GHS09

Signalwort

Warning

Gefahreneinstufungen

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

Lagerklassenschlüssel

13 - Non Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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D Thomas Lowery et al.
Journal of economic entomology, 99(4), 1369-1374 (2006-08-30)
Laboratory bioassays using leaf disks of apple dipped in test solutions of insecticides demonstrated that the apple aphid, Aphis pomi De Geer, and the spirea aphid, Aphis spiraecola Patch, differed significantly in susceptibility to a number of insecticides registered for
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Pest management science, 67(4), 483-491 (2011-01-22)
Pymetrozine is a valuable novel insecticide for control of sucking insects, including the brown planthopper Nilaparvata lugens (Stål), one of the most serious pests on rice. This study was conducted to elucidate the action mechanisms of pymetrozine on the feeding
Doreen Möckel et al.
Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology, 197(2), 193-202 (2010-11-06)
The tympanal organ of the bushcricket Mecopoda elongata emits pronounced distortion-product otoacoustic emissions (DPOAEs). Their characteristics are comparable to those measured in other insects, such as locusts and moths, with the 2f1-f2 emission being the most prominent one. Yet the
Ralf Nauen et al.
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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
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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