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Merck

34084

Supelco

Flocoumafen

PESTANAL®, analytical standard

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About This Item

Empirische Formel (Hill-System):
C33H25F3O4
CAS-Nummer:
Molekulargewicht:
542.54
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Beschreibung

mixture of isomers

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

agriculture
environmental

Format

neat

SMILES String

OC1=C(C2CC(Cc3ccccc23)c4ccc(OCc5ccc(cc5)C(F)(F)F)cc4)C(=O)Oc6ccccc16

InChI

1S/C33H25F3O4/c34-33(35,36)24-13-9-20(10-14-24)19-39-25-15-11-21(12-16-25)23-17-22-5-1-2-6-26(22)28(18-23)30-31(37)27-7-3-4-8-29(27)40-32(30)38/h1-16,23,28,37H,17-19H2

InChIKey

KKBGNYHHEIAGOH-UHFFFAOYSA-N

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Allgemeine Beschreibung

Flocoumafen is a second generation anticoagulant rodenticides, which can have an array of applications in pest control.(1) It belongs to the 4-hydroxycoumarin class of rodenticides.

Anwendung

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

Rechtliche Hinweise

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

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 1 Dermal - Acute Tox. 1 Inhalation - Acute Tox. 1 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1B - STOT RE 1

Zielorgane

Blood

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

73.4 °F

Flammpunkt (°C)

23 °C

Persönliche Schutzausrüstung

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


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Rapid determination of three anticoagulant rodenticides in whole blood by liquid chromatography coupled with electrospray ionization mass spectrometry
Jin C-M and Chen H-X
Rapid Communications in Mass Spectrometry, 20, 2741-2746 (2006)
K R Huckle et al.
Xenobiotica; the fate of foreign compounds in biological systems, 19(1), 51-62 (1989-01-01)
1. 14C-Flocoumafen, administered to Japanese quail as a single oral or i.p. dose, was rapidly and extensively eliminated in excreta; most was eliminated within 24 h. Extensive metabolism of the rodenticide was seen, with at least 8 metabolites detected; unchanged
K R Huckle et al.
Xenobiotica; the fate of foreign compounds in biological systems, 19(1), 63-74 (1989-01-01)
1. Appreciable penetration of radioacticity occurred through rat skin following percutaneous administration of 14C-flocoumafen. At 7 days after dosing 12% of the administered radioactivity remained at the site of application, while 25% was located in the liver as unchanged flocoumafen.
F P Rowe et al.
The Journal of hygiene, 95(3), 623-627 (1985-12-01)
The efficacy of flocoumafen, a novel anticoagulant rodenticide, was evaluated in feeding tests on confined and free-living populations of house mice (Mus musculus L.). In four pen trials, family groups of laboratory-reared wild mice were conditioned to feeding on plain
A P Buckle
The Journal of hygiene, 96(3), 467-473 (1986-06-01)
The anticoagulant rodenticide flocoumafen was tested against warfarin-resistant Norway rats (Rattus norvegicus Berk.) infesting farm buildings. Complete control was obtained in 10-21 days (mean 14.2 days) in six treatments in which baits poisoned with 0.005% flocoumafen were maintained, in surplus

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