33028
Cyanofenphos solution
100 μg/mL in acetonitrile, PESTANAL®, analytical standard
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About This Item
Empirical Formula (Hill Notation):
C15H14NO2PS
CAS Number:
Molecular Weight:
303.32
Beilstein:
2945855
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
Recommended Products
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
concentration
100 μg/mL in acetonitrile
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
agriculture
format
single component solution
storage temp.
2-8°C
SMILES string
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
InChI key
LRNJHZNPJSPMGK-UHFFFAOYSA-N
General description
Cyanofenphos belongs to the class of phosphonothioate insecticides. It is used to control various insect pests in agriculture.
Application
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.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point(F)
35.6 °F
Flash Point(C)
2 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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