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68535

Supelco

Halofenozide

PESTANAL®, analytical standard

Synonym(s):

N-tert-Butyl-N′-(4-chlorobenzoyl)benzohydrazide

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About This Item

Empirical Formula (Hill Notation):
C18H19ClN2O2
CAS Number:
Molecular Weight:
330.81
Beilstein:
8421868
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

Assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

composition

carbon content, 65.35%
hydrogen content, 5.79%
nitrogen content, 8.47%

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CC(C)(C)N(NC(=O)c1ccc(Cl)cc1)C(=O)c2ccccc2

InChI

1S/C18H19ClN2O2/c1-18(2,3)21(17(23)14-7-5-4-6-8-14)20-16(22)13-9-11-15(19)12-10-13/h4-12H,1-3H3,(H,20,22)

InChI key

CNKHSLKYRMDDNQ-UHFFFAOYSA-N

General description

Halofenozide is a systemic type of insect growth regulator belonging to the class of non-steroidal ecdysone agonists. It shows a broad spectrum of activity in controlling beetle grub and lepidopteran larval pests.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Chronic 2 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Insect Control: Biological and Synthetic Agents (2010)
Effects of ecdysone agonist halofenozide against Culex pipiens.
Boudjelida H, et al.
Pesticide Biochemistry and Physiology, 83(2-3), 115-123 (2005)
Ji-Feng Shi et al.
Insect biochemistry and molecular biology, 68, 1-12 (2015-11-26)
Uridine diphosphate-N-acetylglucosamine-pyrophosphorylase (UAP) is involved in the biosynthesis of chitin, an essential component of the epidermal cuticle and midgut peritrophic matrix (PM) in insects. In the present paper, two putative LdUAP genes were cloned in Leptinotarsa decemlineata. In vivo bioassay revealed
Jinhua Gan et al.
Ecotoxicology and environmental safety, 210, 111853-111853 (2021-01-11)
A multi-residue analysis of six diacylhydrazine insecticides in water, sediment, and aquatic products was established by liquid chromatography triple quadrupole tandem mass spectrometry (LC-MS/MS). The water sample was extracted with acetonitrile by low-temperature enrichment liquid-liquid extraction technology. The sediment and
Sayoko Ito-Harashima et al.
FEBS open bio, 7(7), 995-1008 (2017-07-07)
Synthetic nonsteroidal ecdysone agonists, a class of insect growth regulators (IGRs), target the ecdysone receptor (EcR), which forms a heterodimer with ultraspiracle (USP) to transactivate ecdysone response genes. These compounds have high binding affinities to the EcR-USP complexes of certain

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