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Supelco

Imidacloprid

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C9H10ClN5O2
CAS Number:
138261-41-3
Molecular Weight:
255.66
MDL number:
MFCD00468059
UNSPSC Code:
41116107
PubChem Substance ID:
329755710
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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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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
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H301,H410

Hazard Classifications

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

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCJ5226
BCCD6887
BCBZ3018
BCBT2267
SZBE125XV

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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
Mara Andrione et al.
Scientific reports, 6, 38110-38110 (2016-12-03)
Exposure to neonicotinoid pesticides is considered one of the possible causes of honeybee (Apis mellifera) population decline. At sublethal doses, these chemicals have been shown to negatively affect a number of behaviours, including performance of olfactory learning and memory, due
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
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
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Neonicotinoids

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

Banned and Other Neonicotinoids from Plant Material

On Friday, April 27, 2018, the European Union decided to ban the use of three neonicotinoid insecticides from use on field crops, having deemed them dangerous to bees. This application demonstrates the analysis of these banned compounds and others from dandelion blossoms using QuEChERS and LC-MS.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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