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Safety Information

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:
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

Signal Word

Danger

Hazard Statements

H301,H317,H332,H373,H410

Hazard Classifications

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

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

Regulatory Information

农药列管产品

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ6273
BCBX4055

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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
Grant Herron et al.
Experimental & applied acarology, 26(3-4), 253-256 (2003-01-23)
The successful use of chemical rotations to manage insecticide resistance requires reversion between alternate chemical applications. We tested a tebufenpyrad resistant population of Tetranychus urticae Koch after some 55 months laboratory culture without pesticide selection and found LC50 level resistance
Santos Fustero et al.
The Journal of organic chemistry, 73(9), 3523-3529 (2008-04-11)
The preparation of N-methylpyrazoles is usually accomplished through reaction of a suitable 1,3-diketone with methylhydrazine in ethanol as the solvent. This strategy, however, leads to the formation of regioisomeric mixtures of N-methylpyrazoles, which sometimes are difficult to separate. We have
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
Dejan Marcic
Experimental & applied acarology, 36(3), 177-185 (2005-09-01)
Sublethal effects of the mitochondrial electron transport inhibitor (METI) tebufenpyrad on Tetranychus urticae Koch females surviving treatment as eggs or immatures (> or =90% mortality) were investigated in life-table assay. The developmental time of females that had survived treatment as
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