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Flubendiamide

PESTANAL®, analytical standard

Synonym(s):

N2-[1,1-Dimethyl-2-(methylsulfonyl)ethyl]-3-iodo-N1-{2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl}-1,2-benzenedicarboxamide

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About This Item

Empirical Formula (Hill Notation):
C23H22F7IN2O4S
CAS Number:
Molecular Weight:
682.39
Beilstein:
11326832
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

Cc1cc(ccc1NC(=O)c2cccc(I)c2C(=O)NC(C)(C)CS(C)(=O)=O)C(F)(C(F)(F)F)C(F)(F)F

InChI

1S/C23H22F7IN2O4S/c1-12-10-13(21(24,22(25,26)27)23(28,29)30)8-9-16(12)32-18(34)14-6-5-7-15(31)17(14)19(35)33-20(2,3)11-38(4,36)37/h5-10H,11H2,1-4H3,(H,32,34)(H,33,35)

InChI key

ZGNITFSDLCMLGI-UHFFFAOYSA-N

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General description

Flubendiamide is a novel insecticide that is grouped under the family of phthalic acid diamides. It is largely used against lepidopteron pests in various annual and perennial crops.

Application

Flubendiamide may be used as an analytical reference standard for the determination of the analyte in vegetables and fruits by high performance liquid chromatography coupled to ultraviolet detector (HPLC-UV) and HPLC combined with tandem mass spectrometry (MS/MS), respectively.
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

Environment

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Ana M Ares et al.
Food chemistry, 232, 169-176 (2017-05-12)
In this study, a new method has been developed to determine flubendiamide in honey using liquid chromatography coupled to a selective mass spectrometry detector (quadrupole-time-of-flight). An efficient sample treatment involving a solid phase extraction with a C
Dinakaran Venkatachalam et al.
Environmental toxicology and pharmacology, 39(1), 321-326 (2014-12-30)
The disposition kinetics study of cefquinome was conducted following single intravenous (IV) administration of 2mg/kg bodyweight in buffalo calves after oral subchronic exposure to flubendiamide and to determine the in vitro plasma protein binding of cefquinome. Plasma concentrations of cefquinome
Shun-Fan Wu et al.
Pesticide biochemistry and physiology, 146, 1-6 (2018-04-09)
The susceptibilities of three field populations of pink stem borer (PSB), Sesamia inferens (walker) to diamide insecticides, chlorantraniliprole and flubendiamide, were evaluated in this study. The results showed that these PSB field populations were still sensitive to the two diamide
Simple and efficient method for the estimation of residues of flubendiamide and its metabolite desiodo flubendiamide.
Singh B, et al.
Journal of Agricultural and Food Chemistry, 56(7), 2299-2302 (2008)
Rajesh Mandil et al.
Chemico-biological interactions, 260, 91-101 (2016-11-09)
Study was undertaken to evaluate ameliorative potential of α-tocopherol against copper sulphate and flubendiamide alone and in combination-induced toxicity in rats following 90 days exposure. Absolute and relative organ weights did not differ between treatments groups. Increase of LPO in

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