Skip to Content
Merck

Key Documents

View All Documentation

31223

Fenpropathrin

PESTANAL®, analytical standard

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C22H23NO3
CAS Number:
39515-41-8
Molecular Weight:
349.42
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329753687
EC Number:
254-485-0
Beilstein/REAXYS Number:
2673776
MDL number:
MFCD00144305
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

grade

analytical standard

Quality Level

100

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

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

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

Other Notes

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

Still not finding the right product?

Explore all of our products under Fenpropathrin

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

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

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCK2881
BCBZ6259
BCBT7187

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
View All Related Papers