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37894

Supelco

Imidacloprid

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C9H10ClN5O2
CAS Number:
Molecular Weight:
255.66
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
NMR: suitable
gas chromatography (GC): suitable

mp

140-146 °C

suitability

passes test for identity (NMR)

application(s)

agriculture
environmental

format

neat

SMILES string

[O-][N+](=O)NC1=NCCN1Cc2ccc(Cl)nc2

InChI

1S/C9H10ClN5O2/c10-8-2-1-7(5-12-8)6-14-4-3-11-9(14)13-15(16)17/h1-2,5H,3-4,6H2,(H,11,13)

InChI key

YWTYJOPNNQFBPC-UHFFFAOYSA-N

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Related Categories

General description

Imidacloprid is a systemic chloronicotinyl insecticide, which can be effectively used in agriculture to control pests like aphids, scale insects, whiteflies, leafhoppers, some coleoptera and some lepidoptera species.

Find more information here: Neonicotinoids

Application

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

Legal Information

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

Pictograms

Skull and crossbonesEnvironment

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Yixi Zhang et al.
Insect biochemistry and molecular biology, 79, 50-56 (2016-10-30)
Target insensitivity contributing to imidacloprid resistance in Nilaparvata lugens has been reported to occur either through point mutations or quantitative change in nicotinic acetylcholine receptors (nAChRs). However, the metabolic resistance, especially the enhanced detoxification by P450 enzymes, is the major
DDT resistance in Drosophila correlates with Cyp6g1 over-expression and confers cross-resistance to the neonicotinoid imidacloprid
Decourtye A, et al.
Molecular Genetics and Genomics, 266, 556-563 (2001)
Lin-Rui Gao et al.
Journal of agricultural and food chemistry, 64(47), 9078-9088 (2016-10-30)
As a neonicotinoid pesticide, imidacloprid is widely used to control sucking insects on agricultural planting and fleas on domestic animals. However, the extent to which imidacloprid exposure has an influence on cardiogensis in early embryogenesis is still poorly understood. In
Alison R Holt et al.
The Science of the total environment, 573, 1422-1429 (2016-08-20)
Debate about how sustainable intensification and multifunctionality might be implemented continues, but there remains little understanding as to what extent they are achievable in arable landscapes. Policies that influence agronomic decisions are rarely made with an appreciation of the trade-offs
Elise Hughes Berheim et al.
Scientific reports, 9(1), 4534-4534 (2019-03-16)
Over the past decade, abnormalities have been documented in white-tailed deer (Odocoileus virginianus) in west-central Montana. Hypotheses proposed to explain these anomalies included contact with endocrine disrupting pesticides, such as imidacloprid. We evaluated the effects of imidacloprid experimentally at the

Protocols

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

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

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

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

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