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Fenpropathrin

PESTANAL®, analytical standard

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About This Item

Formula empirica (notazione di Hill):
C22H23NO3
Numero CAS:
Peso molecolare:
349.42
Beilstein:
2673776
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

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
XQUXKZZNEFRCAW-UHFFFAOYSA-N

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Descrizione generale

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.

Applicazioni

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.

Prodotti consigliati

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.

Note legali

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

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Pittogrammi

Skull and crossbonesEnvironment

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

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

Codice della classe di stoccaggio

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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


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Certificati d'analisi (COA)

Lot/Batch Number

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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)
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)
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)
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)
Songbai Zhang et al.
Biodegradation, 22(5), 869-875 (2010-12-25)
A novel bacterial strain capable of degrading the pyrethroid pesticide fenpropathrin was isolated from mixed wastewater and sludge samples. Phylogenetic analysis of the 16S rDNA sequence revealed that the organism belongs to the genus Clostridium. The organism can co-metabolically transform

Protocolli

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