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Supelco

Imidacloprid-olefin

PESTANAL®, analytical standard

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C9H8ClN5O2
CAS Number:
115086-54-9
Molecular Weight:
253.65
MDL number:
MFCD02660798
UNSPSC Code:
77101502
PubChem Substance ID:
329755021
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

application(s)

agriculture
environmental

format

neat

storage temp.

2-8°C

SMILES string

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)

InChI key

TYLCDJYHUVCRBH-UHFFFAOYSA-N

General description

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

Find more information here: Neonicotinoids

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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.

Legal Information

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ8453
BCCD7355
BCCB1529
BCBS4509V
SZBF177XV

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Persistence and metabolism of imidacloprid in different soils of West Bengal.
Sarkar AM, et al.
Pest Management Science, 57(7), 598-602 (2001)
Natural Beekeeping: Organic Approaches to Modern Apiculture, 2nd Edition (2013)
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

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