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Supelco

Imidacloprid-olefin

PESTANAL®, analytical standard

Sinonimo/i:

1-[(6-Chloro-3-pyridinyl)methyl]-N-nitro-1H-imidazol-2-amine

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About This Item

Formula empirica (notazione di Hill):
C9H8ClN5O2
Numero CAS:
Peso molecolare:
253.65
Numero MDL:
Codice UNSPSC:
77101502
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

applicazioni

agriculture
environmental

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

ClC1=NC=C(CN2C(N[N+]([O-])=O)=NC=C2)C=C1

InChI

1S/C9H8ClN5O2/c10-8-2-1-7(5-12-8)6-14-4-3-11-9(14)13-15(16)17/h1-5H,6H2,(H,11,13)
TYLCDJYHUVCRBH-UHFFFAOYSA-N

Descrizione generale

Imidacloprid-olefin is a metabolite of the insecticide, imidacloprid.

Find more information here: Neonicotinoids

Prodotti consigliati

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

Exclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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I clienti hanno visto anche

Persistence and metabolism of imidacloprid in different soils of West Bengal.
Sarkar AM, et al.
Pest Management Science, 57(7), 598-602 (2001)
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Maura J Hall et al.
Molecules (Basel, Switzerland), 25(12) (2020-06-18)
Consistent with the large-scale use of pesticide seed treatments in U.S. field crop production, there has been an increased use of neonicotinoid-treated corn and soybean seed over the past decade. Neonicotinoids can move downwind to adjacent off-field pollinator habitats in
Margaret L Eng et al.
The Science of the total environment, 760, 143409-143409 (2020-11-22)
Neonicotinoids are the most widely used insecticides globally, but their rapid metabolism in vertebrates makes diagnosing wildlife exposure challenging. More detailed information on the pattern of imidacloprid metabolites over time could be used to better approximate the timing and level

Protocolli

Learn more about Neonicotinoids - active substances used in plant protection products to control harmful insects.

Analysis of banned neonicotinoid insecticides from dandelion blossoms using QuEChERS and LC-MS.

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