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Documenti fondamentali

33028

Supelco

Cyanofenphos

100 μg/mL in acetonitrile, PESTANAL®, analytical standard

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About This Item

Formula empirica (notazione di Hill):
C15H14NO2PS
Numero CAS:
Peso molecolare:
303.32
Beilstein:
2945855
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

Concentrazione

100 μg/mL in acetonitrile

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture

Formato

single component solution

Temperatura di conservazione

2-8°C

Stringa SMILE

CCOP(=S)(Oc1ccc(cc1)C#N)c2ccccc2

InChI

1S/C15H14NO2PS/c1-2-17-19(20,15-6-4-3-5-7-15)18-14-10-8-13(12-16)9-11-14/h3-11H,2H2,1H3
LRNJHZNPJSPMGK-UHFFFAOYSA-N

Descrizione generale

Cyanofenphos belongs to the class of phosphonothioate insecticides. It is used to control various insect pests in agriculture.

Applicazioni

Cyanofenphos may be used as an analytical reference standard for the determination of the analyte in:
  • Nutraceutical products by liquid chromatography Orbitrap-mass spectrometry (LC-Orbitrap-MS).
  • Animal samples by gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-tandem mass spectrometry (LC-MS/MS).
  • Agricultural products by GC-MS.
  • Fruits and vegetables by GC-MS/MS.

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

Note legali

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

Pittogrammi

FlameExclamation mark

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

35.6 °F

Punto d’infiammabilità (°C)

2 °C

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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S A Soliman et al.
Journal of toxicology and environmental health, 14(5-6), 789-801 (1984-01-01)
Trio-o-cresyl phosphate (TOCP), leptophos [O-methyl O-(4-bromo-2,5,-dichlorophenyl) phenylphosphonothioate] and cyanofenphos [O-ethyl O-(4-cyanophenyl) phenyl-phosphonothioate] were used to determine whether adult peking ducks would exhibit neurotoxicity after exposure to such chemicals. Clinical, histopathological, and specific biochemical tests were used to detect the neurologic
Metabolism of the optical isomers of cyanofenphos in rice stem borer larvae.
Ohkawa H, et al.
Agricultural and Biological Chemistry, 42(2), 445-450 (1978)
Delayed neuropathy in sheep by the phosphonothioate insecticide cyanofenphos.
El-Sebae AH, et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 14(3), 247-263 (1979)
E Enan et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 22(2), 149-170 (1987-04-01)
Male Baladi rabbits were acutely and sub-chronically intoxicated with cyanofenphos and profenophos. The levels of cholesterol, triglycerides, B-lipoproteins and total proteins were determined in the serum, brain, spinal cord and sciatic nerve of rabbits. Moreover, the activities of alkaline phosphatase
A H El-Sebae et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 15(3), 267-285 (1980-01-01)
Delayed neurotoxic ataxia, similar to that caused by neurotoxic organophosphorous compounds, has been shown to occur in hens after oral administration of Cyanofenphos (O-ethyl-O-Cyanophenyl phenyl phosphonothionate) following either single or repeated oral doses. Axonal and myelin degeneration affecting the long

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