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Merck

46037

Supelco

Cyphenothrin

PESTANAL®, analytical standard, sum of isomers

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About This Item

Empirische Formel (Hill-System):
C24H25NO3
CAS-Nummer:
Molekulargewicht:
375.46
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Beschreibung

mixture of cis and trans 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

C\C(C)=C\C1C(C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2)C1(C)C

InChI

1S/C24H25NO3/c1-16(2)13-20-22(24(20,3)4)23(26)28-21(15-25)17-9-8-12-19(14-17)27-18-10-6-5-7-11-18/h5-14,20-22H,1-4H3

InChIKey

FJDPATXIBIBRIM-UHFFFAOYSA-N

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Allgemeine Beschreibung

Cyphenothrin is classified under the synthetic pyrethroid category of pesticides.

Anwendung

Cyphenothrin may be used as a reference standard for the identification of cyphenothrin in:
  • Animal fat samples by ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) equipped with electrospray ionization (ESI) and multiple reaction monitoring (MRM) mode of detection.
  • Indoor air by passive sampling using Tenax Tenax® tubes followed by thermal desorption gas chromatography-mass spectrometry (TD-GC-MS).
  • Urine samples by GC-MS with electron impact (EI) ionization.
  • Fruit matrices by HPLC with ultraviolet (UV) detection.

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Cyphenothrin may be used as a reference standard for the identification of cyphenothrin in:
  • Animal fat samples by ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) equipped with electrospray ionization (ESI) and multiple reaction monitoring (MRM) mode of detection.
  • Indoor air by passive sampling using Tenax® TA tubes followed by thermal desorption gas chromatography-mass spectrometry (TD-GC-MS).
  • Urine samples by GC-MS with electron impact (EI) ionization.
  • Fruit matrices by HPLC with ultraviolet (UV) detection.

Rechtliche Hinweise

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
Tenax is a registered trademark of Buchem B.V.

Piktogramme

Exclamation markEnvironment

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, multi-purpose combination respirator cartridge (US)


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T Itoh et al.
Journal of the American Mosquito Control Association, 8(1), 84-85 (1992-03-01)
Laboratory tests were conducted to determine the effect of different bed net materials, impregnated with permethrin or cyphenothrin, on Culex mosquitoes. Polyethylene, polyester and vinylon nettings were more efficacious than cotton or nylon.
Development of magnetic molecularly imprinted polymers based on carbon nanotubes-Application for trace analysis of pyrethroids in fruit matrices.
Ma G and Chen L
Journal of Chromatography A, 1329(9), 1-9 (2014)
Chien-Che Hung et al.
Environmental science and pollution research international (2018-06-07)
We conducted a pilot study to examine pesticides in dust of homes in a rural county of Taiwan. A total of 56 homes of pregnant women were included in the study. Indoor and outdoor dust was collected by a vacuum
Mary H Grace
Phytotherapy research : PTR, 16(2), 183-185 (2002-04-05)
The volatile fractions obtained by hydrodistillation of the fresh leaves of Anthemis melampodina and Pluchea dioscoridis were analysed by GC-MS technique. Of 38 components identified in the volatile oil of A. melampodina, santolinatriene was the major component (27.33%). The oil
Efficacy of Cyphenothrin (Gokilaht-S 5% EC) as space spray against mosquitoes in sentinel cages.
P K Mittal et al.
Journal of vector borne diseases, 46(3), 241-243 (2009-09-03)

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