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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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Certificates of Analysis (COA)

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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)
Tanya Cáceres et al.
Chemosphere, 66(7), 1264-1269 (2006-08-26)
The acute toxicity of an organophosphorous pesticide, fenamiphos and its metabolites, fenamiphos sulfoxide, fenamiphos sulfone, fenamiphos phenol, fenamiphos sulfoxide phenol and fenamiphos sulfone phenol, to a cladoceran, Daphnia carinata was studied in both cladoceran culture medium and natural water collected
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)
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

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