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33028

Supelco

Cyanofenphos solution

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

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About This Item

Empirical Formula (Hill Notation):
C15H14NO2PS
CAS Number:
13067-93-1
Molecular Weight:
303.32
Beilstein:
2945855
EC Number:
200-835-2
MDL number:
MFCD00055313
UNSPSC Code:
41116107
PubChem Substance ID:
329754441
NACRES:
NA.24

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

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PDSCL

Deleterious substance

FSL

Group 4: Flammable liquids
Type 1 petroleums
Hazardous rank II
Water insoluble liquid

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

33028-BULK:
33028-2ML:4548173985213
33028-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
BCBV4522
SZBC199XV
SZBB024XV
SZBB024X
SZE9217X

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High-pressure liquid chromatography of neurotoxic phenylphosphonothioate esters and related compounds.
J M Lasker et al.
Analytical biochemistry, 109(2), 369-375 (1980-12-01)
Determination of toxic substances, pesticides and mycotoxins, in ginkgo biloba nutraceutical products by liquid chromatography Orbitrap-mass spectrometry.
Martinez-Dominguez G, et al.
Microchemical Journal, Devoted to the Application of Microtechniques in All Branches of Science, 118(2), 124-130 (2015)
N Konno et al.
The Tohoku journal of experimental medicine, 142(2), 155-163 (1984-02-01)
Cyanofenphos (Surecide, O-ethyl O-4-cyanophenyl phenylphosphonothioate) is an organophosphorus pesticide. The protective effect against the near lethal dose, 140% the LD50, of formulated cyanofenphos developed in hens pretreated daily with a small dosage of 1.4% the LD50. The oral LD50 for
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)
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