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45483

Supelco

Fenamiphos

PESTANAL®, analytical standard

Synonym(s):

Phenamiphos

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About This Item

Empirical Formula (Hill Notation):
C13H22NO3PS
CAS Number:
Molecular Weight:
303.36
Beilstein:
4752893
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

storage temp.

2-8°C

SMILES string

CCOP(=O)(NC(C)C)Oc1ccc(SC)c(C)c1

InChI

1S/C13H22NO3PS/c1-6-16-18(15,14-10(2)3)17-12-7-8-13(19-5)11(4)9-12/h7-10H,6H2,1-5H3,(H,14,15)

InChI key

ZCJPOPBZHLUFHF-UHFFFAOYSA-N

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General description

Fenamiphos is a non-fumigant nematicide, which is widely used for controlling nematodes in agricultural fields.

Application

Fenamiphos may be used as a reference standard in the determination of fenamiphos in water samples using high-performance liquid chromatography (HPLC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Legal Information

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

Pictograms

Skull and crossbonesEnvironment

Signal Word

Danger

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Persistence and effects of fenamiphos on native algal populations and enzymatic activities in soil.
Megharaj M, et al.
Soil Biology and Biochemistry, 31(11), 1549-1553 (1999)
Panneerselvan Logeshwaran et al.
Chemosphere, 252, 126549-126549 (2020-04-02)
Fenamiphos is a neurotoxic organophosphorus pesticide used widely to control pests of crops. Fenamiphos and its toxic oxidation products have been detected in surface and groundwaters. A novel enzyme capable of hydrolysing P-O-C bond of fenamiphos is purified from Microbacterium
Transformation and adsorption of fenamiphos, f. sulfoxide and f. sulfone in Molokai soil and simulated movement with irrigation.
Lee C-C, et al.
Journal of Contaminant Hydrology, 1(1-2), 211-225 (1986)
Dimitrios Georgios Karpouzas et al.
Environmental toxicology and chemistry, 23(9), 2099-2107 (2004-09-24)
The application of fenamiphos either alone or in combination with soil fumigants is a common practice in greenhouses and potato-cultivation areas in Greece. However, repeated applications of fenamiphos in the same field for a number of years can lead to
Marie Lecoeur-Lorin et al.
Electrophoresis, 30(16), 2931-2939 (2009-08-05)
The enantioseparation of fenamiphos and its two main metabolites (fenamiphos sulfoxide and fenamiphos sulfone) were simultaneously achieved by CE by using a dual CD system. A mixture of 25 mM carboxymethyl-beta-CD and 10 mM hydroxypropyl-alpha-CD was added to the acetic

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