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Thiacloprid

PESTANAL®, analytical standard

Synonym(s):

[3-(6-Chloro-3-pyridinylmethyl)-2-thiazolidinylidene]cyanamide

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About This Item

Empirical Formula (Hill Notation):
C10H9ClN4S
CAS Number:
111988-49-9
Molecular Weight:
252.72
MDL number:
MFCD02101042
UNSPSC Code:
41116107
PubChem Substance ID:
329755719
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
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

Clc1ccc(CN2CCS\C2=N\C#N)cn1

InChI

1S/C10H9ClN4S/c11-9-2-1-8(5-13-9)6-15-3-4-16-10(15)14-7-12/h1-2,5H,3-4,6H2/b14-10+

InChI key

HOKKPVIRMVDYPB-GXDHUFHOSA-N

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General description

Thiacloprid is a chloronicotinyl insecticide, which can be commonly used in agriculture in order to control various sucking insects like aphids, whiteflies and some jassids. It can also be actively used against weevils, leaf miners and various species of beetles.

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

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Repr. 1B - STOT SE 3

Target Organs

Central nervous system

Storage Class Code

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

WGK

WGK 3

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)

Lot/Batch Number
BCCG2065
BCBW6020
BCBT5886
SZBD234XV
SZBC180XV

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Céline Lukowicz et al.
Environmental health perspectives, 126(6), 067007-067007 (2018-06-29)
Epidemiological evidence suggests a link between pesticide exposure and the development of metabolic diseases. However, most experimental studies have evaluated the metabolic effects of pesticides using individual molecules, often at nonrelevant doses or in combination with other risk factors such
Dissipation rates of iprodione and thiacloprid during tomato production in greenhouse
Omirou.M, et al.
Food Chemistry, 116, 499-504 (2009)
Makoto Ihara et al.
British journal of pharmacology, 175(11), 1999-2012 (2017-06-16)
Neonicotinoid insecticides interact with the orthosteric site formed at subunit interfaces of insect nicotinic ACh (nACh) receptors. However, their interactions with the orthosteric sites at α-non α and α-α subunit interfaces remain poorly understood. The aim of this study was
Jochen P Zubrod et al.
Environmental science & technology, 51(16), 9280-9287 (2017-07-07)
Disturbance regimes determine communities' structure and functioning. Nonetheless, little effort has been undertaken to understand interactions of press and pulse disturbances. In this context, leaf-shredding macroinvertebrates can be chronically exposed to wastewater treatment plant effluents (i.e., press disturbance) before experiencing
Effects of thiacloprid, a new chloronicotinyl insecticide, on the egg parasitoid Trichogramma cacaoeciae
Schuld M and Schmuck R
Ecotoxicology (London, England), 9, 197-205 (2000)
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