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Supelco

Tefluthrin

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C17H14ClF7O2
CAS Number:
Molecular Weight:
418.73
Beilstein:
8398039
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

description

mixture of isomers

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

Cc1c(F)c(F)c(COC(=O)C2C(\C=C(/Cl)C(F)(F)F)C2(C)C)c(F)c1F

InChI

1S/C17H14ClF7O2/c1-6-11(19)13(21)7(14(22)12(6)20)5-27-15(26)10-8(16(10,2)3)4-9(18)17(23,24)25/h4,8,10H,5H2,1-3H3/b9-4-/t8-,10-/m0/s1

InChI key

ZFHGXWPMULPQSE-UKSCLKOJSA-N

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General description

Tefluthrin is a synthetic soil pyrethroid insecticide, which can be actively used against corn rootworms and cut worms. It can also be widely used to control a large variety of pests that affect maize and sugar beet crop.

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. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

329.0 °F

Flash Point(C)

165 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Desorption of tefluthrin insecticide from soil in simulated rainfall runoff systems?Kinetic studies and modelling
Zhou.LJ, et al.
Water Research, 31(1), 75-84 (1997)
Underlying mechanism of actions of tefluthrin, a pyrethroid insecticide, on voltage-gated ion currents and on action currents in pituitary tumor (GH 3) cells and GnRH-secreting (GT1-7) neurons
Wu N-S, et al.
Toxicology, 258(1), 70-77 (2009)
Chin-Wei Huang et al.
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 47(1), 330-343 (2018-05-17)
Rotenone (Rot) is known to suppress the activity of complex I in the mitochondrial chain reaction; however, whether this compound has effects on ion currents in neurons remains largely unexplored. With the aid of patch-clamp technology and simulation modeling, the
Yong Wen et al.
Journal of agricultural and food chemistry, 67(42), 11591-11597 (2019-09-27)
A simple and eco-friendly dispersive solid-phase extraction method coupled with ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was developed for the determination of the chiral pesticide tefluthrin in food and environmental samples. The response surface methodology was applied to optimize
Rukshan V Mehta et al.
BMC public health, 20(1), 1877-1877 (2020-12-09)
Population growth which has resulted in a need for increased crop yields to sustain food security, in addition to the effects of climate change, have led to the widespread use of chemical pesticides. The indiscriminate use of pesticides has in

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