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46438

Supelco

Tebufenpyrad

PESTANAL®, analytical standard

Synonym(s):

4-Chloro-N-(4-tert-butylbenzyl)-3-ethyl-1-methyl-1H-pyrazole-5-carboxamide

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About This Item

Empirical Formula (Hill Notation):
C18H24ClN3O
CAS Number:
119168-77-3
Molecular Weight:
333.86
Beilstein/REAXYS Number:
8636471
MDL number:
MFCD01632408
UNSPSC Code:
41116107
PubChem Substance ID:
329757184

grade

analytical standard

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

CCc1nn(C)c(C(=O)NCc2ccc(cc2)C(C)(C)C)c1Cl

InChI

1S/C18H24ClN3O/c1-6-14-15(19)16(22(5)21-14)17(23)20-11-12-7-9-13(10-8-12)18(2,3)4/h7-10H,6,11H2,1-5H3,(H,20,23)

InChI key

ZZYSLNWGKKDOML-UHFFFAOYSA-N

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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

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Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1B - STOT RE 2

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ6273
BCBX4055
SZBD324XV
SZBC220XV
SZBA088XV

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Santos Fustero et al.
The Journal of organic chemistry, 73(21), 8545-8552 (2008-10-16)
In previous studies, our group has shown that the use of fluorinated alcohols such as trifluoroethanol (TFE) and hexafluoroisopropanol (HFIP) as solvents dramatically increases the regioselectivity in the pyrazole formation from 1,3-diketone with methylhydrazine. We have now applied this synthetic
M A Ali et al.
Journal of economic entomology, 96(2), 259-263 (2004-03-05)
We evaluated three concentrations of tebufenpyrad (17.5, 15 and 12.5%) in strip formulations for controlling varroa mites, Varroa destructor Anderson and Trueman (2000), in honey bee colonies. We also included colonies treated with Apistan, CheckMite+, and untreated colonies in our
Hongjian Song et al.
Journal of agricultural and food chemistry, 60(6), 1470-1479 (2012-02-07)
On the basis of commercial insecticides tebufenpyrad and tolfenpyrad, two series of novel pyrazole-5-carboxamides containing α-hydroxymethyl-N-benzyl or α-chloromethyl-N-benzyl and pyrazoles containing 4,5-dihydrooxazole moieties were designed and synthesized via the key intermediate 2-amino-1-(4-substituted) phenyl ethanol. The structures of target compounds were
N Stumpf et al.
Journal of economic entomology, 94(6), 1577-1583 (2002-01-05)
Resistance of the twospotted spider mite, Tetranychus urticae Koch, to acaricides acting as mitochondrial electron transport inhibitors (METIs) is an increasing problem. Because of their high levels of cross-resistance to all commercially available METI-acaricides, a Japanese strain (AKITA) and an
G J Devine et al.
Pest management science, 57(8), 749-750 (2001-08-24)
The naphthoquinones and the METI group of compounds act on sites associated with mitochondrial respiration, but METI-resistant strains of two-spotted spider mite from Japan and the UK exhibited no cross-resistance to the naphthoquinones. The potential for developing commercial naphthoquinones therefore
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