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Fenpropathrin

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C22H23NO3
CAS Number:
Molecular Weight:
349.42
Beilstein:
2673776
EC Number:
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

storage temp.

2-8°C

SMILES string

CC1(C)C(C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2)C1(C)C

InChI

1S/C22H23NO3/c1-21(2)19(22(21,3)4)20(24)26-18(14-23)15-9-8-12-17(13-15)25-16-10-6-5-7-11-16/h5-13,18-19H,1-4H3

InChI key

XQUXKZZNEFRCAW-UHFFFAOYSA-N

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General description

Fenpropathrin is a synthetic pyrethroid insecticide used in veterinary medicine and also for crop protection in agriculture. Pyrethroid insecticides act by disrupting nerve function and produce acute neurotoxic effects in both insects and non-target organisms.

Application

Fenpropathrin may be used as an insecticide reference standard for the determination of the analyte:
  • In vegetables using high-performance liquid chromatography with a photochemically-induced post-column method, and fluorescence detection and using gas chromatography with electron capture detector (GC-ECD).
  • In Chinese tea by gas chromatography–mass spectrometry (GC–MS) method following the extraction with acetone–ethyl acetate–hexane, clean-up using gel permeation chromatography (GPC) and solid-phase extraction (SPE).

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

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

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. 2 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - 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)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number

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Simultaneous determination of 102 pesticide residues in Chinese teas by gas chromatography- mass spectrometry.
Huang Z, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 853(1-2), 154- 162 (2007)
The 28-day exposure to fenpropathrin decreases locomotor activity and reduces activity of antioxidant enzymes in mice brains.
Nieradko-Iwanicka B and Borzecki A
Pharmacological Reports, 68(2), 495- 501 (2016)
A gas chromatographic method with electron-capture detector (GC-ECD) for simultaneous determination of fenpropathrin, lambda-cyhalothrin, and deltamethrin residues in tomato and its applications to kinetic studies after field treatment.
Albadri et al.
Food Analytical Methods, 5(6), 1296- 1302 (2012)
Toxic effects of five insecticides and their mixture on male albino rats.
Mansour SA, et al.
Journal of the Egyptian Society of Toxicology, 39(2), 85- 94 (2008)
Zhaoyany Li et al.
Chemosphere, 76(4), 509-516 (2009-04-10)
Fenpropathrin and fenvalerate are two widely used pyrethroid insecticides. Due to one and two asymmetrical centers, fenpropathrin and fenvalerate consist of two and four stereoisomers, respectively. In the present study, the degradation of fenpropathrin and fenvalerate in two soils, an

Protocols

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